SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs76901441 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60337245 | TCACCAGCACTAATA[C/G]GAAAATATCCTACTA | 84669 |
rs76938499 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | USP32 | GRCh38.p7 | 17:60229622 | TGAAAGAGTAACAGC[A/G]CCACCTTTGAGAAAA | 84669 |
rs76940479 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60237598 | CCCCATTACCCACTT[C/T]GCCCAGACCTTAACA | 84669 |
rs77024136 | snp | C/T | 0.00431734 | 0.0462605 | missense | USP32 | GRCh38.p7 | 17:60185651 | CATGCTCATCTACAA[C/T]CTGCAGGTAGAGGGA | 84669 |
rs77064129 | snp | A/G | 0.029116 | 0.117091 | intron-variant | USP32 | GRCh38.p7 | 17:60263912 | CTAAACCTCTATTTA[A/G]TAACACCATTGTGGT | 84669 |
rs77064220 | snp | C/G | 0.0547245 | 0.156101 | intron-variant | USP32 | GRCh38.p7 | 17:60286501 | AGGCAAGGAATAATT[C/G]TTTTCTAGGGACTGA | 84669 |
rs77113104 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP32 | GRCh38.p7 | 17:60283953 | AAATAACTTTTATTT[C/T]AAAAGTAGGTGGTAA | 84669 |
rs77145086 | snp | A/G | 0.5 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414870 | CTTTTTTTTTTTTTT[A/G]GATGGAGTCTTGCTC | 84669 |
rs77201739 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60400301 | ATCTCTGACTGCTGT[A/G]TTGAAAGTGGACTGG | 84669 |
rs77211692 | snp | C/T | 0.106278 | 0.204558 | intron-variant | USP32 | GRCh38.p7 | 17:60236902 | TTTGTGGTTCATCTA[C/T]TATTGTGGCAGACAT | 84669 |
rs77232762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337088 | AGGGATTTAATCAAT[A/C]ATATAGATCAACTAT | 84669 |
rs77243263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60281176 | TTCTCTGAAGACAGA[A/G]GGGTAAAAACCACTG | 84669 |
rs77264293 | in-del | -/AAAAAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60386379 | TAAAAAAAAAAAAAA[-/AAAAAT]CCCTCCACCACTGCA | 84669 |
rs77292300 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60302596 | TCTGCATATTACAGA[C/T]CCACACAACTGAATT | 84669 |
rs77298743 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60366877 | ACCCAGGCTGGAGTG[A/C]CAGGGTGCGATCTCG | 84669 |
rs77299884 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60385839 | TAGAGACTCTGTCTC[A/C]AAAAAAAAAAAAGAA | 84669 |
rs77341051 | snp | G/T | 0.5 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416933 | TCCTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTC | 84669 |
rs77416668 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295820 | CTTTATCATAGATAC[A/G]TATGTATAGGAAGAA | 84669 |
rs77462919 | snp | C/T | 0.030278 | 0.119257 | intron-variant | USP32 | GRCh38.p7 | 17:60387718 | AAGTTGAAAATATCA[C/T]TAAGTCAAAAATGTA | 84669 |
rs77474435 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60368870 | GACTTCATATAATGC[A/G]ATCCAAGTTTCTCTG | 84669 |
rs77512064 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60398814 | AAGACCCTGTCTCTA[A/C]AAAAAAAAAAAATTT | 84669 |
rs77564057 | snp | C/T | 0.106633 | 0.204807 | intron-variant | USP32 | GRCh38.p7 | 17:60252937 | TATATTAATTGCATA[C/T]ATTAATTGTACATAT | 84669 |
rs77649115 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60356743 | TTAAAATGTCTCATT[C/T]TCAACAAAAAATTGC | 84669 |
rs77652295 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60389903 | GCACCTATAGTCCCA[A/G]CTGCTGGGGAGGCTG | 84669 |
rs77652880 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60346896 | CTACAGCAAAGCACG[A/G]AGTAGCAAACGATAA | 84669 |
rs77664204 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60184731 | AAGAGAATCACTTGA[G/T]CCCGAGAGGTGGAGG | 84669 |
rs77673476 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309235 | AATCCCTTGTCAGAT[C/G]GATACTTTGCAAATA | 84669 |
rs77693548 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60391562 | AGGGGGGCTGGATGG[C/G]CTGGAGCCGCCCAAG | 84669 |
rs77714183 | snp | C/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60271317 | CAGGTATGTTTACCA[C/G]TGAACATATGTAGAA | 84669 |
rs77719366 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60336715 | AGCGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 84669 |
rs77761822 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414997 | GCTGGGATTACAGGA[A/T]GAAATTTAAAACAAA | 84669 |
rs77765775 | snp | A/T | | | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266012 | GTCCTTCCAGACTTC[A/T]AAAAGTGCAACCACC | 84669 |
rs77792840 | snp | A/G/T | 1.64898e-05 | 0.00287135 | missense, synonymous-codon | USP32 | GRCh38.p7 | 17:60223522 | ACACTGGTTGTTATT[A/G/T]TCAGAAGTGTTATGT | 84669 |
rs77847606 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60221257 | AAATTAGCTGTTATG[G/T]TGGTGTGTGCCTGCA | 84669 |
rs77853457 | snp | A/C | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60281538 | GAGACTCCGTCTCAA[A/C]AAAAAAAAAAAATGC | 84669 |
rs77879262 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | USP32 | GRCh38.p7 | 17:60352481 | GTGAGAAAAATAAAC[C/G]CTTATATCTTATTTA | 84669 |
rs77906461 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | USP32 | GRCh38.p7 | 17:60338077 | GCCTTGTAATCCAGT[A/C]CCCTGGGAGGCTAGG | 84669 |
rs77923584 | in-del | -/GA | 0.379158 | 0.214052 | intron-variant | USP32 | GRCh38.p7 | 17:60340349 | GGGAGGCCAAGGTGG[-/GA]GAGGATCATTTGAGC | 84669 |
rs77947567 | in-del | -/CTCGCAAGTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60326431 | TTCTCCTGCCTCAGC[-/CTCGCAAGTA]GCTGGGATTACAGGC | 84669 |
rs77948831 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60354756 | TGAATCCAAAAAAGT[A/C]TGATATAAGGCCAGG | 84669 |
rs77965831 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60356244 | AGCAGTGGCAGATGG[G/T]GCTAACAAGAGGTTA | 84669 |
rs78013849 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60283298 | CACGTGAGGAGAAAT[A/G]AGCATGGGAAATTAA | 84669 |
rs78025849 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60384805 | CCAAAAAAAAAAAAA[-/AA]TCCCTAAAATAAAGA | 84669 |
rs78038914 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60223952 | GAAAAATATTCCAAA[C/T]GTTCTTGGTAGATAA | 84669 |
rs78073575 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408279 | ACTATATTTAAAGAA[A/G]AACATGAATATAATG | 84669 |
rs78084217 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60228044 | TCTTTTTTTTTTTTT[G/T]AGACAGAGTCAAGCT | 84669 |
rs78092459 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60262139 | CATATGAACTTTTTC[G/T]AAAGCAAATTCACTG | 84669 |
rs78097279 | snp | G/T | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60297843 | AATATTGAAAACAGT[G/T]GCAGCTCATTCACCA | 84669 |
rs78111417 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306147 | TAATAGGCAGTCCTT[C/T]AACATTTAGAGAATA | 84669 |
rs78146118 | snp | A/G | | | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231602 | TTGGCCTCCAGCCTT[A/G]GCTAAGGAGAACAGG | 84669 |
rs78147168 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60298370 | AGGCTATAACCCTTT[A/G]TAAGAAATAAAGTTT | 84669 |
rs78169939 | snp | A/C | 0.375 | 0.216506 | intron-variant | USP32 | GRCh38.p7 | 17:60266388 | GGGCGAAGTTACTGT[A/C]CAATAAATATTACAA | 84669 |
rs78191558 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | USP32 | GRCh38.p7 | 17:60249011 | TAGAGTTTATCTTCC[A/G]GTACAGTATCTTGCA | 84669 |
rs78193875 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60293836 | AATTGTGTCAAAAAG[C/T]CACCCAAAAGAAAAT | 84669 |
rs78198604 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60334107 | ATGGAGATGATTAGC[A/G]CCTCGAATACTTACA | 84669 |
rs78232094 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60199148 | AAAGATGCCAGTGGA[A/G]AAAAAAAAAAAAGAC | 84669 |
rs78275779 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424370 | ATGAATCCCTGTTCA[G/T]TCCCCCAAGGAGCTG | 84669 |
rs78305932 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60348397 | ATATGGAATAGTCAG[G/T]AGAAAAGAAGGAGAA | 84669 |
rs78358085 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60362152 | CCCCATCTGCCACTA[C/T]TTCTGTTCCCCCAGC | 84669 |
rs78358174 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | USP32 | GRCh38.p7 | 17:60314801 | TACATTCCTGAAAAA[C/T]AGTAATACAGAAAAT | 84669 |
rs78421770 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408786 | GAAGCAAGCATGCAA[C/T]GATAGGGGGAATCTA | 84669 |
rs78454582 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60329492 | TTTATTTTTTTTTTT[G/T]GAGATGAGGTCTCAC | 84669 |
rs78472943 | snp | A/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60250019 | AAATGAATAAACAAA[A/T]TTTAAAAAAAACCCA | 84669 |
rs78479487 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60394347 | CTACTATTATTACTG[G/T]CCTAAACCGTCAGTA | 84669 |
rs78498204 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378331 | AAATGGAAGGAGCAC[G/T]TGTGCATTGCTGGTG | 84669 |
rs78509635 | snp | A/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60372681 | CCCGTTCTCTACATT[A/T]AAAAAAAAAAAAGAA | 84669 |
rs78512980 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP32 | GRCh38.p7 | 17:60257887 | AACAGTTTTAGTTTC[A/G]GCTTCTTACTAAGTT | 84669 |
rs78514675 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60311994 | TTAAGTGACAGATAC[C/T]GTTTTATCATGGCTT | 84669 |
rs78550825 | snp | A/G | 0.0547245 | 0.156101 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295278 | TGTCAACAAGAGAAC[A/G]GGTAAAATGAGATAC | 84669 |
rs78554998 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60372556 | GATAAAAAAAAAAAA[-/AA]GTCCAGGCACGGTGG | 84669 |
rs78599343 | snp | A/C | | | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271435 | CCGGGATTGAGCCTT[A/C]AATAACCAATAGCGT | 84669 |
rs78605124 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60292884 | TCACGCTGTCCTATA[A/G]GACAATATATAATCA | 84669 |
rs78627372 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264859 | AGCAAGACTCTGTCA[A/C]AAAAAAAAAAAAAAA | 84669 |
rs78629371 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60228043 | TTCTTTTTTTTTTTT[G/T]GAGACAGAGTCAAGC | 84669 |
rs78655817 | snp | G/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60373462 | TTTTTTTTTTTTTTT[G/T]AGACCAAGTCTTGCT | 84669 |
rs78694817 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60289661 | CACGCCAATCCCTTT[A/G]CTTGGAAGACAAGAG | 84669 |
rs78722654 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423194 | TTCTTTTTTTCTTTG[G/T]TCTTTTTTTTTTTTT | 84669 |
rs78785651 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60237214 | GGTGCAATCTCAGCT[C/T]GCTGAAGCCTTGACC | 84669 |
rs78799708 | snp | C/T | 0.0858192 | 0.188533 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232052 | ACAATTAGTAATATT[C/T]GTAAGTAAATATGTC | 84669 |
rs78809010 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60336716 | GCGAGACTCCATCTC[A/C]AAAAAAAAAAAAAAG | 84669 |
rs78811246 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60220662 | CTTTTTTTTTTTTTT[G/T]AGACACAGTCTCGCT | 84669 |
rs78812326 | snp | A/G | 0.00538163 | 0.0515932 | intron-variant | USP32 | GRCh38.p7 | 17:60249687 | TCCATTGTTCTCACC[A/G]AGGATTAGTAGTTCT | 84669 |
rs78832134 | snp | C/T | 0.104859 | 0.203554 | intron-variant | USP32 | GRCh38.p7 | 17:60387592 | ATTATTAAACATACA[C/T]AAGTTAGAACTATAA | 84669 |
rs78847608 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60387675 | TGATACAACTTACAA[C/T]GAGATTACCTCCCAA | 84669 |
rs78862134 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60293289 | ATGTCTGCATAAACC[A/G]TATTAAAATGAAAAA | 84669 |
rs78898529 | snp | A/T | 0.105924 | 0.204309 | intron-variant | USP32 | GRCh38.p7 | 17:60365731 | TATTAAAAGAATGCA[A/T]TAAGATAAACCATTT | 84669 |
rs78900541 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60229327 | GGATTACAGGCATGA[A/G]TCACCCGGCCAAAGG | 84669 |
rs78941555 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60383660 | TGAGAATGAGCCAGA[C/T]ATGTAAAAATTCATA | 84669 |
rs78975773 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60299776 | TACCATAAACTGGGT[A/G]CTTATAAATAACAGA | 84669 |
rs78976337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60235133 | TACGGAAAACAAAAC[A/G]TAATACATCCAAGAC | 84669 |
rs78980193 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60327154 | CCAACACAAAGAAAT[A/G]ACAAATGTTTGAGAT | 84669 |
rs79005843 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60220661 | CCTTTTTTTTTTTTT[G/T]GAGACACAGTCTCGC | 84669 |
rs79021418 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | USP32 | GRCh38.p7 | 17:60224039 | AGTAATGGGGGCTAG[A/T]TCCTATTGTATCTAT | 84669 |
rs79021874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60218964 | GAGCAAGTCTTGCCC[A/G]TCAATAAAGTTTAAC | 84669 |
rs79029332 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60322002 | GTTGAGAAAACTTAA[C/T]AAACAGAAATAAATA | 84669 |
rs79030592 | snp | G/T | 0.5 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403029 | ATCTCTGTTTTTTTT[G/T]TGAGACGGAGTCTCG | 84669 |
rs79041272 | snp | A/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60246413 | TGTATATATATATAT[A/T]TTTTTTTTTTTTCTT | 84669 |
rs79056307 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60355012 | TAGCGCCACCGCACC[C/G]CAGCCTGGGCAACAT | 84669 |
rs79067269 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60373441 | AATTTTAGCTTACTG[G/T]AATTTTTTTTTTTTT | 84669 |
rs79089047 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60198106 | CTCCTACTCCAAATA[G/T]CAAACCAAATGGTTG | 84669 |
rs79098808 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60256586 | CCATGTCTGCATGAA[A/T]TTTCTCCAGGTACTC | 84669 |
rs79113768 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60317674 | TTCAAGAATTAGCTA[C/G]GTGTAGTGCCATGCA | 84669 |
rs79117509 | snp | C/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60210299 | CATTAGTTTCATTCA[C/T]TCATCCTTCTACTTT | 84669 |
rs79128132 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60383236 | GACAGACATCGTCCC[A/C]AAAAAAAAAAAAAAA | 84669 |
rs79160035 | snp | A/G | 0 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407805 | AAAAAAAAAAAAAAA[A/G]AGCAGAAACAGGCCG | 84669 |
rs79195447 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305298 | AGCAGAGAACAAGCA[A/T]GTCACATGGTGAGAG | 84669 |
rs79201147 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421018 | CTTAGGACTAATTCC[C/T]CCTATAAGTAGAATT | 84669 |
rs79205391 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413102 | AAAACTACAGTAAAT[A/G]TCAGATAAGAGTGAA | 84669 |
rs79207248 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60277443 | TGTAAGCCTTGCATC[A/C]CTAACGGATAAGAGG | 84669 |
rs79210680 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60395248 | AAGATTTCCTCTTTA[A/C]GTTTCAGGCCTGGCA | 84669 |
rs79233939 | snp | A/C | 0.248755 | 0.249997 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407472 | AGGTCTAAACTAGGT[A/C]TAGAGTAAAGTACAC | 84669 |
rs79272653 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60240094 | AGCTCTTTGAACATA[C/T]TTAAGATAATTGATT | 84669 |
rs79295220 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | USP32 | GRCh38.p7 | 17:60400885 | TTTAAAAATTAGCTT[A/G]ATATGGTGCCACCTG | 84669 |
rs79328572 | snp | A/G | 0.077417 | 0.180873 | intron-variant | USP32 | GRCh38.p7 | 17:60192162 | TGGGTACAGTGGTGT[A/G]CACCTGTAGTCCCGG | 84669 |
rs79370602 | snp | G/T | 0.269267 | 0.249256 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417463 | TTTTAATTTTTTTTT[G/T]TTTTTTTGTGACAGA | 84669 |
rs79379609 | snp | A/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60246411 | TGTGTATATATATAT[A/T]TATTTTTTTTTTTTC | 84669 |
rs79422508 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232568 | TTTTTTTTTTTTTAA[A/T]TACAGTCTCATTCTG | 84669 |
rs79429298 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265116 | AGGTTAGCCTTACCA[C/T]AACTTAGTCAAATGG | 84669 |
rs79468780 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60234045 | GTCTTGACCTATCAG[A/G]CTCAAGCAATCCTCC | 84669 |
rs79470411 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264857 | AGAGCAAGACTCTGT[A/C]AAAAAAAAAAAAAAA | 84669 |
rs79483098 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60335311 | TGCAAATATTAAGTA[C/T]GTGTCTGTCTTTCTT | 84669 |
rs79485136 | snp | C/T | 0.0135563 | 0.0812057 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422564 | ACGTGGGGAGTGCCA[C/T]CCTGGAGCCTACCGG | 84669 |
rs79506968 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414851 | ATTTTTCTTTTCTTT[A/C/T]TTTCTTTTTTTTTTT | 84669 |
rs79519684 | snp | C/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60312751 | AAGAACTTGATGTCA[C/G]CAACCTACATGCTTA | 84669 |
rs79574693 | snp | A/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60303545 | CTAAAAAAAAAAAAG[A/T]AACCCTAGAATGGAA | 84669 |
rs79583756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60397320 | TGGCTTTGATTTCTT[C/T]ATCTTGTGGATGAGA | 84669 |
rs79597866 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60225953 | GTGAAACTCAGTCTC[A/C]AAAAAAAAAAAAAAA | 84669 |
rs79632058 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | USP32 | GRCh38.p7 | 17:60240887 | ACAGAACTTCTGACG[A/G]ATAACCCTGCCTGCC | 84669 |
rs79685010 | snp | A/G | 0.00260821 | 0.036018 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231552 | AAGGCTGCCCCACTC[A/G]TGGCAGTCCTGACGA | 84669 |
rs79701708 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60184809 | AGTGAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 84669 |
rs79703401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60396917 | GTATCTCCTTCAAAT[C/T]AATAGTTTACAAAGG | 84669 |
rs79708659 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210322 | TTCTACTTTTTTTTT[A/C/T]CTTTTTGGAGACAGA | 84669 |
rs79723967 | snp | C/T | 0.5 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414855 | TTCTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTA | 84669 |
rs79732897 | snp | A/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60202443 | AATCAGCTTATCAAA[A/T]CACACACACACACAC | 84669 |
rs79800762 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60390089 | CTATCTCTTCAAATA[A/C]ATGTGTTTTAAAATT | 84669 |
rs79801306 | snp | A/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60372679 | ACCCCGTTCTCTACA[A/T]TAAAAAAAAAAAAAG | 84669 |
rs79813353 | snp | A/G | 0.0779248 | 0.181356 | missense, intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422626 | CAAGGGGGTGAAGGG[A/G]ACAAGCCACTAGAGC | 84669 |
rs79817016 | snp | A/T | 0.5 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403885 | TGTCTACAAAAAATT[A/T]AAAAATTAGCCAGGC | 84669 |
rs79851920 | snp | C/T | 0.00764794 | 0.0613635 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231625 | AGAACAGGGACCCCC[C/T]AAAGCCCATGGGAGA | 84669 |
rs79857482 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60384124 | AAAGGGAGGAACTGA[A/G]GATATGTCTAGATTT | 84669 |
rs79861141 | snp | A/C | 0.5 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412534 | AGTGATACCCTGTTT[A/C]AAAAAAAAAAAAAAA | 84669 |
rs79864283 | snp | C/T | 0.029116 | 0.117091 | intron-variant | USP32 | GRCh38.p7 | 17:60364714 | TTCATGAATTTACAA[C/T]CATTTACTATGTCCA | 84669 |
rs79865750 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60360281 | GAGTTTGACACCAGC[C/G]TGGCCACCATGGCAA | 84669 |
rs79866252 | snp | C/G | 0.030278 | 0.119257 | intron-variant | USP32 | GRCh38.p7 | 17:60252729 | ACATTACCTCAGGAA[C/G]AGATTTCAGAATAAT | 84669 |
rs79884210 | snp | C/T | 0.105569 | 0.204058 | intron-variant | USP32 | GRCh38.p7 | 17:60241534 | TGGGCAGTTTGTTCT[C/T]TATTTTTCAATGTTT | 84669 |
rs79885247 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60191794 | GATTACACGCGTGAG[C/G]CACCACGCCTGGCCA | 84669 |
rs79920206 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60283579 | TCTAATATGAAGCTT[A/G]ACAAGGAAAAGTCAA | 84669 |
rs79935942 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP32 | GRCh38.p7 | 17:60313599 | CCAGGGATTAGAAAG[C/T]GGAATAGTACCCAAA | 84669 |
rs79950654 | snp | G/T | 0.273856 | 0.248859 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417469 | TTTTTTTTTTTTTTT[G/T]TGTGACAGAGTCTCG | 84669 |
rs79954866 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60330567 | TCTCTTTTTTTTAAA[G/T]ACAGGTTCTCACTCT | 84669 |
rs79958986 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | USP32 | GRCh38.p7 | 17:60398055 | TTTGAAAGCTATAAA[A/G]TAGCATTTAGTTAAA | 84669 |
rs80012888 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60344644 | CTGTTTTTAAGTAGA[A/G]ATGAGGTCTCACTAT | 84669 |
rs80019625 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60289489 | CTCCTAGAGTAGACA[A/T]TCAGGATCCCAGAAG | 84669 |
rs80057311 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60368516 | CTAGTTACAGGGCCA[C/T]TGCGGTTGGGGGGCG | 84669 |
rs80080676 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | USP32 | GRCh38.p7 | 17:60292963 | TATTGTTCCTTGGAC[A/G]TACAAGTACACCCCC | 84669 |
rs80110102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60243007 | TTTCAAATCCATTTA[C/T]GTACATTTTCTTAAA | 84669 |
rs80115238 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60327031 | AGAAAAGTACAGCCA[A/G]ATAGGAGGGAAAAGT | 84669 |
rs80123555 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407385 | ACAAATTATGACCAA[C/T]TGGAGTAGAAATAAC | 84669 |
rs80141586 | snp | A/C | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60300153 | GTTCAAGAATAAAAG[A/C]AAAGGAATTTTGGGT | 84669 |
rs80142904 | snp | A/C | 0.00027114 | 0.0116403 | synonymous-codon, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269556 | AAAAGCATTAAACAA[A/C]CCTGTAAAATAGGAA | 84669 |
rs80154564 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60394900 | AGGCGCACACCATCC[C/T]GCCCGGCTAATTTTT | 84669 |
rs80174765 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | USP32 | GRCh38.p7 | 17:60272958 | CTATGTACAAATGCC[A/G]GGAAATTTGTTTTGT | 84669 |
rs80207453 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231326 | TTTGGAAAAATAGAG[C/G]GCAGCATGGAGCAAC | 84669 |
rs80212228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60311014 | GTAGTGGGGAGGAGG[A/G]GGGAATACAGATAAG | 84669 |
rs80219541 | snp | A/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60350026 | TTTTGTTTTTTTTTT[A/T]ATTTTGAGACGGGAT | 84669 |
rs80228045 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402651 | TACCTGTGCTACTGT[C/G]ATTCTGGGTTGTCAT | 84669 |
rs80278607 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60354686 | GCAAGAGGGGGCCTA[C/T]AACTAGCAATTTTTT | 84669 |
rs80328813 | snp | G/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60180029 | ATTAACTAACTCCTG[G/T]TTTTTTTTTTTCTTG | 84669 |
rs80346569 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60274707 | ACAGATTTTTTTTTT[G/T]GACAAATGAAGTGTT | 84669 |
rs111232092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60399483 | AACATAGCAAGAGCC[C/T]GTCTCTACAAAAAAA | 84669 |
rs111282078 | snp | A/C/T | 0.000399281 | 0.0141238 | splice-acceptor-variant | USP32 | GRCh38.p7 | 17:60214776 | AGAAGGTACATTTCC[A/C/T]ATGGTTACAGTAATC | 84669 |
rs111297286 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60319511 | AGCTAGGCACAGTAG[C/T]TCATGCCTGTAATCC | 84669 |
rs111297586 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60336648 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 84669 |
rs111324705 | in-del | -/A | 0.140581 | 0.224783 | intron-variant | USP32 | GRCh38.p7 | 17:60256176 | GACACCATCTCTTTG[-/A]AAAAAAAAATAATAA | 84669 |
rs111328492 | snp | C/T | 0.5 | 0 | synonymous-codon | USP32 | GRCh38.p7 | 17:60198436 | CAGGAAATACAGTTC[C/T]GTCCTCATCTGTATG | 84669 |
rs111330712 | in-del | -/ACCCAGC | 0.287606 | 0.247155 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422013 | CACATCCCACCCAGT[-/ACCCAGC]ACCCAGCACCCAGCA | 84669 |
rs111335380 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, synonymous-codon, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421489 | AAGAACAGGGCCACA[A/C/T]TGAGTGGGGACAACT | 84669 |
rs111369805 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60227246 | CTATTTCTGGCAAGC[A/G]ACACTAGTTTTCTTT | 84669 |
rs111374350 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60195833 | CTCCAGCAGAGGACA[G/T]TCAAGTGAATTTCCC | 84669 |
rs111402906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416029 | ATTTTTAGTAGAGAC[A/G]GGGTTTCAGCATGTT | 84669 |
rs111424514 | in-del | -/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60227583 | TCAGTTTTTCTTTTC[-/T]TTTTTTTTTTTTTGA | 84669 |
rs111427866 | snp | A/G | 0.0596104 | 0.162024 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417599 | GCTGGGATTACAGGT[A/G]CCTGCCACCACACCC | 84669 |
rs111445359 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60362667 | TGACTATTTAACATA[A/T]GTTGATGACAAATGT | 84669 |
rs111480037 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414096 | GGCTGGGCGTGGTGG[C/G]TCACGCCTATAATCC | 84669 |
rs111482227 | snp | C/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60260716 | ATAGAAAATTATATA[C/T]AGATTTAGGAAAATT | 84669 |
rs111491865 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60358158 | TACTTTTTTATTGCA[A/C]ATATAGAGTATTTCA | 84669 |
rs111492991 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393716 | TGAGACGGAGTTTCA[C/T]CCCTGTTGCCCAGGC | 84669 |
rs111493965 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60202685 | TATTCCTAGGTACTT[A/G]ATTTTTTCTCAGCAT | 84669 |
rs111499378 | snp | C/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60330530 | TCTCCCCCCCTCCCT[C/T]CTTTCTCTCTTTCTC | 84669 |
rs111499716 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60218359 | ACTCCACTTCAGCCT[A/G]GGCGACAGAGCAAGA | 84669 |
rs111525421 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60334623 | CCTGAACCCGGGAGG[C/G/T]GGAGCTTGCAGTGAG | 84669 |
rs111532419 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60264241 | AAAAAATTTTTTAGG[C/T]CAGCACAGTGGCTCA | 84669 |
rs111538514 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60343065 | ATCTTGGGCCATTAC[A/G]TAATGGTAAAGGGAT | 84669 |
rs111555075 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60210704 | GTCCACCTTGCAGTT[A/G]GAATACTGCTAATAG | 84669 |
rs111556971 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60267233 | CAACATGGTGAAATC[C/T]CGTCGCTACTAAAAA | 84669 |
rs111559688 | snp | A/T | 0.0626037 | 0.165477 | intron-variant | USP32 | GRCh38.p7 | 17:60234743 | CTCAGAAAAAAAAAA[A/T]TTTTTTTTTGTTTTG | 84669 |
rs111586105 | snp | C/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60255298 | GAACATCTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 84669 |
rs111590733 | in-del | -/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60237116 | AAAAAATCTACTCTA[-/C]TCTATCTATCTATCT | 84669 |
rs111594383 | in-del | -/A | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60348765 | GAGCGAGACTGTCTT[-/A]AAAAAAAAAAAAGAT | 84669 |
rs111605710 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60357289 | GACCCCATCTCTACA[A/T]AAAATAAATAATAAT | 84669 |
rs111648674 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60380031 | AAAATACTCAAATAC[A/G]AAGGATCCAAATGTA | 84669 |
rs111675414 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402287 | ACAGAGTCTCACTCT[C/G]TTGCCCAGGCTGGAG | 84669 |
rs111697501 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409286 | CTAGGAGGCGGAGGT[G/T]GCAGTGAGCCGAAAT | 84669 |
rs111710231 | in-del | -/A | 0.190205 | 0.242744 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295241 | AAGAGCAAAACTTCG[-/A]AAAAAAAAAAAGATA | 84669 |
rs111794547 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60188787 | GGGCAATAATCCCAA[A/T]TTAAACCACGGTATC | 84669 |
rs111804260 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60360345 | TTTTGTATTTTTACA[A/C]ATACAAAAAATTTTT | 84669 |
rs111845103 | snp | C/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60379679 | ATTATAAACTTCAGT[C/T]ACATTGCTATAAAAT | 84669 |
rs111858139 | in-del | -/A | 0.132066 | 0.220435 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306086 | TTTTCACTCAAAAAG[-/A]AAAAAAAAAGGAAAA | 84669 |
rs111888206 | snp | C/T | 0.077417 | 0.180873 | intron-variant | USP32 | GRCh38.p7 | 17:60200142 | TAGAGTACAGTGAGC[C/T]GAGATCGTGCCATTG | 84669 |
rs111893871 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60391618 | CACATCCAGGATCAC[A/G]ACGCCACCAGCGAGC | 84669 |
rs111900408 | snp | A/G | 0.5 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408318 | AGAAAAAAGAACCAG[A/G]TGGAACTTCTAGTGG | 84669 |
rs111906586 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378010 | CTGTAACCCACAGAA[A/G]TATTTGGGAGAAAAT | 84669 |
rs111911459 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410561 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 84669 |
rs112006098 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | USP32 | GRCh38.p7 | 17:60315643 | TATTCACAGCAGCAT[C/T]ATTGACAATAGAAGA | 84669 |
rs112006539 | snp | C/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60220664 | TTTTTTTTTTTTTGA[C/G]ACACAGTCTCGCTCT | 84669 |
rs112015986 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | USP32 | GRCh38.p7 | 17:60279933 | TTGATTAAAAAATTA[A/G]TTAAGATGTATTAAA | 84669 |
rs112053240 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377978 | CCATGAAAGACAATC[C/T]ACAGATATTAATATA | 84669 |
rs112054536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60284201 | TTTCAAATAATTCAA[C/G]ATTTTTTCTTTTCTT | 84669 |
rs112091512 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60250492 | TCACTATAGCCACAT[A/G]AAAGCCTTTATGTAT | 84669 |
rs112091573 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60379545 | TCTCAAACTGACACA[A/C]ATACATGAGATGCGC | 84669 |
rs112103106 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60332254 | CGAGATGCTGTCTCA[A/G]GAAAGAAAAAAGTGT | 84669 |
rs112119691 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | USP32 | GRCh38.p7 | 17:60394754 | TTTATTTATTTATTT[A/T]TTTTTTTGAGACGGA | 84669 |
rs112131503 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60345611 | TCTACATCTGTAACT[C/G]CAATTCAGAAACAGA | 84669 |
rs112135325 | snp | G/T | 0.0524604 | 0.153226 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393042 | ACATTGATATTGTTT[G/T]GCATCCATTGCCACG | 84669 |
rs112143993 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378887 | GCCACTAATTGTACA[C/T]TTTTTAAAATAGTTC | 84669 |
rs112161223 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60375965 | TGTATCTTCCTATGT[A/G]TGTAATCAAAAAATA | 84669 |
rs112180612 | snp | A/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60343015 | CTGCATCGATCACGC[A/T]GGGAGCTGCAGACCA | 84669 |
rs112185254 | snp | A/T | 0.0310518 | 0.120672 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394074 | TTCCAGTTCACTGTG[A/T]GGTGGTTAATTTTAA | 84669 |
rs112196642 | snp | C/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60310025 | CTCCAGCCTGGGTGA[C/T]AGAGCAAGACTCCAT | 84669 |
rs112201486 | in-del | -/TTAA | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60236522 | TTTCCAATTAATTAA[-/TTAA]TTAATTACATTTTTT | 84669 |
rs112204924 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60287098 | GAGGTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 84669 |
rs112233389 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60267146 | GGCATGGTGGCTCAC[A/G]CCTGCAATCCCAGTA | 84669 |
rs112269738 | snp | C/T | 0.084364 | 0.187256 | intron-variant | USP32 | GRCh38.p7 | 17:60246813 | CATTTTTTCATATAT[C/T]TGCTGGCCATTTGTA | 84669 |
rs112322802 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60302931 | AGTTCTTTGTTGAGT[A/G]CCTACTATCTGCCAG | 84669 |
rs112329702 | snp | A/G | 0.0013558 | 0.0260011 | synonymous-codon | USP32 | GRCh38.p7 | 17:60226226 | AATTACCACAGGGTT[A/G]GCATCCTAAAATCAG | 84669 |
rs112334573 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60194167 | TCCCACATCAGCCTC[C/T]CAAGTAGCTAGGATT | 84669 |
rs112346215 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60308503 | GACCAATGGACGACA[A/G]AGAACCCAGATATAA | 84669 |
rs112346293 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60275913 | AGACCTTGTCTCTAT[A/T]TAAAAAAAAAAAAAA | 84669 |
rs112346360 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60329484 | TGTTTTTATTTATTT[A/T]TTTTTTTTGAGATGA | 84669 |
rs112369454 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60394889 | GCTGGGATTATAGGC[A/G]CACACCATCCCGCCC | 84669 |
rs112375424 | in-del | -/AAAT/AAATAAAT | 0.5 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411324 | GCAAAACTGTCTCAA[-/AAAT/AAATAAAT]AAATAAATAAATAAA | 84669 |
rs112376238 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | USP32 | GRCh38.p7 | 17:60395022 | GTACTGGGATTAGAG[G/T]CACGAGCCACCACGC | 84669 |
rs112405591 | snp | C/T | 0.138886 | 0.22395 | intron-variant | USP32 | GRCh38.p7 | 17:60299031 | TAGCTACTTGGGAGG[C/T]TGAGGTAGGTGGATC | 84669 |
rs112406424 | snp | A/C | 0.0588605 | 0.161139 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421828 | ACTTTCGCCGACACC[A/C]GGCTCCCCGCCTGGT | 84669 |
rs112411192 | snp | A/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60226311 | AAACAAATCTCACAA[A/T]TATCTATTTTTTTAA | 84669 |
rs112413567 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60213945 | TACGTTTTGTTTTTT[G/T]TTTTTTTTTTTTTTA | 84669 |
rs112423624 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60222287 | AATCCACACAGGTTC[A/G]GAACACTCTTCTACC | 84669 |
rs112429970 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60219187 | ATGTTTTGCCAAAAA[A/G]CCAAACAACAACAAA | 84669 |
rs112463179 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | USP32 | GRCh38.p7 | 17:60198051 | GAATGGAAGGATTAT[C/T]TGACACTAGAATGTT | 84669 |
rs112464113 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | USP32 | GRCh38.p7 | 17:60198645 | AAAGGGGCTGAGGTA[C/T]TGCCAGTTTTAGAGT | 84669 |
rs112473482 | in-del | -/A | 0.5 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413056 | AAACATTGCTACAGG[-/A]AAAAAAAAAGTGAAA | 84669 |
rs112496447 | snp | G/T | | | intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179431 | CCGGGTGAAGTTCCT[G/T]AAAGGGCAAGAAAAA | 84669 |
rs112501199 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60361661 | AGTTTCTACAATTCA[A/G]CTTTTTAAAAATTAT | 84669 |
rs112518269 | snp | A/G/T | 0.00358938 | 0.0422398 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403157 | GCTGGGTCTACAGGC[A/G/T]CGCGCCACCACGCCC | 84669 |
rs112522271 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60375122 | AAATAAGTTTTACAA[A/G]AGTGCTGTTGGTGGC | 84669 |
rs112525191 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | USP32 | GRCh38.p7 | 17:60400228 | CCTCGGCCTCCAGAA[A/G]TTCTGAGATTACAGG | 84669 |
rs112527134 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378497 | GATATTTGTACACCA[A/G]TGTTCACAACAACAT | 84669 |
rs112551554 | snp | C/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60375950 | AAAGACAGAAAAATT[C/T]GTATCTTCCTATGTG | 84669 |
rs112551638 | in-del | -/A | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60338343 | AAAAAAAAAAAAAAT[-/A]CTACATAGAAATGTT | 84669 |
rs112559958 | snp | A/C | 0.0861826 | 0.188849 | intron-variant | USP32 | GRCh38.p7 | 17:60341655 | TTTCATTGATTTGAT[A/C]TTCGATCACTGATAC | 84669 |
rs112560951 | snp | C/T | 0.0528381 | 0.153711 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179181 | CTTGCCTTTCAGTGA[C/T]GCTTTTGCCAAATGT | 84669 |
rs112584197 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60332572 | AGAATCGCTTGAACC[A/C]AGGAGGCGGAGACTG | 84669 |
rs112589951 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60180480 | AGTCCATTATTTCAA[A/C]AAATGTTCCCCAGTT | 84669 |
rs112593048 | snp | C/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60371435 | AGCCAGGTGCGGTGG[C/T]ACACGCCTATATAAT | 84669 |
rs112601410 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | USP32 | GRCh38.p7 | 17:60261431 | GCGGGTGGATCACTT[A/G]AGGTCAGGAGTTTGA | 84669 |
rs112608834 | snp | A/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60374993 | TAAACACTAATTTGA[A/T]AAAAGAGTAACAGCA | 84669 |
rs112609916 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60240886 | TACAGAACTTCTGAC[A/G]AATAACCCTGCCTGC | 84669 |
rs112611110 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | USP32 | GRCh38.p7 | 17:60288108 | AACAGAGGGAGACTT[C/T]GTCTCAAAAAAAAAA | 84669 |
rs112640722 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60315188 | GGAATGCCTGAGCTC[A/C]GGAGTTCAAAACCAG | 84669 |
rs112641290 | snp | A/T | 0.0524604 | 0.153226 | intron-variant | USP32 | GRCh38.p7 | 17:60367616 | AGTTCAAGACCAGCT[A/T]GGCCACCATGGCAAA | 84669 |
rs112648343 | snp | C/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60272063 | CAAGCAGTCCTCTCA[C/G]CTCTGCTTCCCAAAG | 84669 |
rs112650493 | in-del | -/A | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60370765 | AAATGCTACTGTCTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs112658702 | in-del | -/TC | 0.135825 | 0.222405 | intron-variant | USP32 | GRCh38.p7 | 17:60249067 | TTTTCTTTTTTATTA[-/TC]TCTGTTTTTATTTTT | 84669 |
rs112664641 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | USP32 | GRCh38.p7 | 17:60399592 | TGCCTGAGCCCAGGA[A/G]GTGGAGGCTCCAGTA | 84669 |
rs112684324 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | USP32 | GRCh38.p7 | 17:60395163 | TCCTTTGACTGAAAC[A/T]CGACTGTAGCTCATG | 84669 |
rs112701088 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60292003 | CCAGCAATTTTTTAA[G/T]TCCACAGGACCTACA | 84669 |
rs112729780 | in-del | -/T | 0.331874 | 0.236213 | intron-variant | USP32 | GRCh38.p7 | 17:60297448 | ATGTTTTTCCTTTTC[-/T]TTTTTTTTTTTTCTT | 84669 |
rs112734506 | in-del | -/T | 0.320575 | 0.239832 | intron-variant | USP32 | GRCh38.p7 | 17:60373549 | CCTGGGTTCAAGCAA[-/T]TCTCGTGCCTCAGCC | 84669 |
rs112743613 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60357392 | CAGGAGTTGGAGGCT[A/G]CAGTGAGCTATGATT | 84669 |
rs112744529 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60252703 | GAAGGAAGAAAAAGC[C/G]AAAGGGGAAGACATT | 84669 |
rs112745256 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60316342 | TCCCACTTGCAGTCA[C/T]TTACTTAGGTAGCTT | 84669 |
rs112758447 | snp | A/T | 0.084364 | 0.187256 | intron-variant | USP32 | GRCh38.p7 | 17:60340533 | CTTGGTAGATCTTTC[A/T]CCATCCCTTTATTTT | 84669 |
rs112784819 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60395532 | ATGCAGTACTTAAGT[C/G]TAATAACGTAGAAAG | 84669 |
rs112791796 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378480 | AAAGCAGGACTCAGA[C/T]AGATATTTGTACACC | 84669 |
rs112794655 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60279050 | AGAGGGAAGAACTGT[A/G]CTAACTTATTTCAAA | 84669 |
rs112795347 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264860 | GCAAGACTCTGTCAA[A/G]AAAAAAAAAAAAAAA | 84669 |
rs112800336 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60289143 | CTCCTGAGTAGCTGG[A/G]ACTACAGGCACCCAC | 84669 |
rs112800759 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233639 | AAACATTTTTAAAAA[A/C]TCTGTCAGTGTGCAG | 84669 |
rs112818052 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | USP32 | GRCh38.p7 | 17:60192551 | GCGATTCTCCTGCCT[C/T]AGTCTCCCAAGTAGC | 84669 |
rs112818809 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60257166 | AAAAAGGAGATGGGA[G/T]TCCAGCTCAAGTCTG | 84669 |
rs112819714 | in-del | -/AATT | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60236512 | ACAACTGGTGTTTCC[-/AATT]AATTAATTAATTAAT | 84669 |
rs112820197 | snp | A/G | 0.0588605 | 0.161139 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421176 | CTCGCAAAATAATCT[A/G]GAATTAATGATCAGA | 84669 |
rs112822370 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406572 | CCAGGCTGGAGTGCA[A/T]TGGCATGACCTCGGC | 84669 |
rs112827548 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378543 | AAAGGTGGAAACAAC[C/T]CAAATATGTCCCATC | 84669 |
rs112833680 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | USP32 | GRCh38.p7 | 17:60289240 | GTCTTGATCTCCTGA[A/C]CTTGTGATCTGCCCG | 84669 |
rs112842442 | snp | C/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60376031 | CAATCTTTTGCCAAT[C/T]ATAATCTAATTTTTT | 84669 |
rs112859029 | snp | A/C | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60225895 | GAAGGTGGAGGTTGC[A/C]GTGAGCAGAGATCGC | 84669 |
rs112859416 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60245280 | CATAAAACATGCATA[A/T]GAGCTGTCTATTCAT | 84669 |
rs112859538 | snp | C/G | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60297230 | TAGCGAGACCCCTAT[C/G]TCTACAAAAAATTTA | 84669 |
rs112892104 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60230326 | AATGAAACCATTCCT[G/T]TAATAATGCTTCTCA | 84669 |
rs112895667 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60292583 | ATACGAGAAAAAATT[C/T]TAGGCCAACTCTACC | 84669 |
rs112898467 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | USP32 | GRCh38.p7 | 17:60343564 | CTACTGGGTAAATAA[C/T]GAAATGAAGGCAGAA | 84669 |
rs112909736 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60343859 | CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 84669 |
rs112918106 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60285584 | CATGTCTCCTAACTC[A/G]TAGGATCCTTTCCGG | 84669 |
rs112918509 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60189270 | CTAGAAAGGGCTCCC[A/G]GGAGCCTTGGTGTGT | 84669 |
rs112925886 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60379693 | TCACATTGCTATAAA[A/C]TTCCAAATTGGGAGT | 84669 |
rs112933038 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410603 | AACCTGGGAGGCGGA[A/G]CTTGCAGTGAGCCGA | 84669 |
rs112937397 | snp | A/T | 0.0554779 | 0.157039 | intron-variant | USP32 | GRCh38.p7 | 17:60253787 | AAATAAATAAATAAA[A/T]AATAAAAAATAGTTG | 84669 |
rs112939543 | snp | C/T | 0.084728 | 0.187577 | intron-variant | USP32 | GRCh38.p7 | 17:60297509 | GTTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC | 84669 |
rs112945866 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60379120 | AGCCATAATCCTATT[A/G]CAGTCAAAATCATAA | 84669 |
rs112949570 | in-del | -/A | 0.258288 | 0.249863 | intron-variant | USP32 | GRCh38.p7 | 17:60335565 | TGAATGGTGAAGTAG[-/A]AAAAAATATATCTAC | 84669 |
rs112957616 | snp | A/T | 0.021333 | 0.101051 | intron-variant | USP32 | GRCh38.p7 | 17:60273960 | GAGCGAGACTCAGTC[A/T]CAAAAAAAAAAAAAA | 84669 |
rs112957797 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378942 | TATATATATATTCAC[A/C]ATAAAAATAAAATAA | 84669 |
rs112994170 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264532 | AAAAAACAAACAGAC[-/A]AAAAAAAAAACAAAA | 84669 |
rs112995905 | in-del | -/T | 0.0592355 | 0.161582 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406517 | AAGTTCTTCTTTTGC[-/T]TTTTTTTCTCTTTTT | 84669 |
rs113005505 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60375017 | AACAGCAAATAATTA[A/G]CTGTGTTTGGTGATG | 84669 |
rs113006047 | in-del | -/T | 0.376592 | 0.215579 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416921 | TATATATCCAATTCC[-/T]TTTTTTTTTTTTTTG | 84669 |
rs113037530 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419102 | CACAATAGCAAAGAC[A/G]TGGAATCAACCTAAA | 84669 |
rs113046248 | snp | C/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60228505 | TTTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTAA | 84669 |
rs113054250 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60254476 | GAGGCTGAGACAGAA[A/G]AACTACTTGAGCCTA | 84669 |
rs113058231 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378962 | AAATAAAATAAATTG[C/G]CAAAGCCAGGAGAAG | 84669 |
rs113078960 | snp | A/G | 0.346368 | 0.23068 | intron-variant | USP32 | GRCh38.p7 | 17:60334675 | CCAGCCTGGGCAACA[A/G]AGCGAGACTCCGTCT | 84669 |
rs113079719 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60196963 | AGGTAGGTGGATTAC[C/T]TGAGGCCAGGAGTTC | 84669 |
rs113092127 | in-del | -/TGT | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295996 | AAGGACACATAAACA[-/TGT]TGTATAAAAACCAGC | 84669 |
rs113098615 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60257183 | CCAGCTCAAGTCTGT[C/T]TCCCTGTGCTTGTTT | 84669 |
rs113100960 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377488 | CTTACAGCAATTGGG[C/T]TAAGAAAGGTTAAAT | 84669 |
rs113109088 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60258538 | GCGTGACAAAAGTGA[C/T]TTTGTTGTTGATCCT | 84669 |
rs113139623 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60347987 | ATTAGCCAGGCCTGG[G/T]GGCGGGCACCTGTAG | 84669 |
rs113139835 | snp | G/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60244039 | ATTGTGTTTTTTTTT[G/T]TTTTTTTTTTTTTTG | 84669 |
rs113169154 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60284453 | TCTCGAACTCCTAAC[C/T]TTGTGATCCGCCCGC | 84669 |
rs113178925 | in-del | -/AAGAT | 0.5 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414355 | GTGACAGAGCAAGAC[-/AAGAT]GTTATCTTTAGTTTC | 84669 |
rs113228710 | snp | C/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60345231 | TCATGGAAATGTTCC[C/T]ATGATCATAATCAGT | 84669 |
rs113254040 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60309430 | CATGGCAGAAACCCC[C/T]GTCTCTACAAAAAAT | 84669 |
rs113267729 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60379025 | TGAAGATCAGACAAA[A/G]ATTCACATGAACTAT | 84669 |
rs113294055 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | USP32 | GRCh38.p7 | 17:60199070 | ACAGTGAGCTGTGAT[C/T]GTGCCACTGCACTCC | 84669 |
rs113297876 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232476 | TTGCACCTGGCCCAA[A/T]TTTTTTTTTTTTTTT | 84669 |
rs113306332 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60374287 | ACGTATTGTCCCACT[A/G]GAAAGTCTTCAGGGC | 84669 |
rs113313081 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60331624 | ATTTAAAGTATACAA[G/T]TGAGGTCAGGCACAG | 84669 |
rs113334845 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60199102 | GCCTGGAAGGTAGAG[C/T]GAGACCTGTCTCAAA | 84669 |
rs113338113 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415830 | ATATGCTTGGTGGTG[G/T]TTTTTTTGTTTATTT | 84669 |
rs113343610 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | USP32 | GRCh38.p7 | 17:60273828 | AGCTGGGCGTGGTGG[C/T]GGGTGCCTGTAGTCC | 84669 |
rs113352377 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60267578 | TGTCACCCAGGCTGG[A/C]GTGCAGTTCTCAGCT | 84669 |
rs113379045 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60379259 | CAAAGTAGCACTGGC[A/C]TAAATTGAGGCAAAT | 84669 |
rs113382873 | snp | A/G | 0.131381 | 0.220067 | intron-variant | USP32 | GRCh38.p7 | 17:60200649 | AACAGAATATAGCGA[A/G]CACTCAAAAGCCTCC | 84669 |
rs113387130 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60275877 | CCACCATGCCTGGCT[A/G]ATTTTTTGTATTTTT | 84669 |
rs113390027 | snp | A/G | 0.084364 | 0.187256 | intron-variant | USP32 | GRCh38.p7 | 17:60286037 | GCTACTTGGGAGGCT[A/G]AGGCAAGAGAATCAC | 84669 |
rs113396508 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413790 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC | 84669 |
rs113408126 | snp | A/G | 0.126909 | 0.217598 | intron-variant | USP32 | GRCh38.p7 | 17:60196003 | TGGGCCGGGTGCAGC[A/G]GCTCACGCCTGTAAT | 84669 |
rs113413455 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60239819 | GATCACTACAACCTC[C/T]GCCTCCCGGGTTCAA | 84669 |
rs113429434 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60379002 | AGCTATGTACATACC[C/T]GAGTTTGTGAAGATC | 84669 |
rs113431523 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | USP32 | GRCh38.p7 | 17:60189415 | GAATGCTTTAAAAAA[C/T]AGTAAAGGAAATTTC | 84669 |
rs113433185 | snp | A/G | 0.198324 | 0.244601 | intron-variant | USP32 | GRCh38.p7 | 17:60334687 | ACAAAGCGAGACTCC[A/G]TCTCAAAAAAAAAGA | 84669 |
rs113440014 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405383 | AATTTTTTTTGTATT[G/T]TAGTAGAGATGGGGT | 84669 |
rs113454063 | in-del | -/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60329480 | ATTTGTTTTTATTTA[-/T]TTTTTTTTTTTTGAG | 84669 |
rs113513048 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60379975 | TGGGAGAGTAAATTA[A/C]TACACATAAAACATG | 84669 |
rs113513951 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60194066 | TTTTTTTTTTGAGAC[A/G]GGGTATCACTCTGTT | 84669 |
rs113540158 | snp | G/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60262585 | GTTCTACTTGAATCT[G/T]TGGAGGTTTCTCCAT | 84669 |
rs113546748 | in-del | -/ATTATT | 0.5 | 0 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419818 | TCAAGGTTAAAAAAA[-/ATTATT]ATTATTATTATTATT | 84669 |
rs113556293 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | USP32 | GRCh38.p7 | 17:60202524 | ATTAAGTCATCCGTA[C/G]ATTAGTTTGTAGAGA | 84669 |
rs113582001 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233245 | CCAAGGCAGGAGAAT[C/T]GCTTGAGCCCAGGAG | 84669 |
rs113591501 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60315382 | TCCACACTCCAGCCT[A/G]GGCGACAGAGTGAGA | 84669 |
rs113597175 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60379085 | AGACATAGTTGAAAA[C/T]ATAATACTGATCATG | 84669 |
rs113598031 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | USP32 | GRCh38.p7 | 17:60388255 | TTATTACTACAATTT[A/G]AAAGTTAAGAATCAT | 84669 |
rs113608142 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60331573 | CCCATCTCAAAAAAA[A/G]ATAAAATAAACTTTA | 84669 |
rs113625393 | snp | A/G | 0.5 | 0 | synonymous-codon | USP32 | GRCh38.p7 | 17:60223506 | CATTGGCTCCCAGCA[A/G]ACACTGGTTGTTATT | 84669 |
rs113634396 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264863 | AGACTCTGTCAAAAA[A/C]AAAAAAAAAAAAAAA | 84669 |
rs113654324 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378506 | ACACCAATGTTCACA[A/G]CAACATTATTCACAA | 84669 |
rs113668247 | snp | C/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60379351 | CTGAAAAATCCACCT[C/G]TAGTATTTTGACTTC | 84669 |
rs113675314 | snp | C/T | 0.0513262 | 0.151752 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417522 | GCAGTGCCATGATCT[C/T]GGCTCACTACAACAT | 84669 |
rs113681537 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | USP32 | GRCh38.p7 | 17:60241324 | AACTCTATAAATAAG[A/G]TATGTTCTGCTCTCT | 84669 |
rs113693415 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406547 | TTGAGACAGAGACTT[A/G]CTCTGTCACCCAGGC | 84669 |
rs113699009 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60206682 | CATTAAATTACATAT[A/T]ATATTGGATTTCTTT | 84669 |
rs113700865 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60218500 | CAAGTACTTCTTTTG[C/G]TCAGGGTTTAGAGGT | 84669 |
rs113706834 | snp | C/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60245839 | ATGTCTTTAGTTCAC[C/T]TTCTTTTTTTTTTAA | 84669 |
rs113708729 | snp | C/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60195134 | ATCTTTTTTAATGTC[C/T]GAAGGACATAACCCA | 84669 |
rs113710288 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | USP32 | GRCh38.p7 | 17:60373466 | TTTTTTTTTTTGAGA[C/T]CAAGTCTTGCTTTGA | 84669 |
rs113715657 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60222807 | CTGCCTCAGCCTCCC[A/G]AGTATCTGGGATTAC | 84669 |
rs113743603 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60371429 | AAAATCAGCCAGGTG[C/T]GGTGGCACACGCCTA | 84669 |
rs113747602 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60379924 | GTCCAATGTGGTTTT[A/C/T]AAAAAAGGTTACTCT | 84669 |
rs113759758 | in-del | -/A | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60385839 | TAGAGACTCTGTCTC[-/A]AAAAAAAAAAAAGAA | 84669 |
rs113762196 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378954 | CACAATAAAAATAAA[A/G]TAAATTGGCAAAGCC | 84669 |
rs113764494 | snp | A/C | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60379293 | TTTTTAACTAGTAGG[A/C]GATAACTGTGAAGGA | 84669 |
rs113787687 | snp | A/G | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60252188 | ATTTTAATGTTAAAT[A/G]GAATTTGCCTTCTTA | 84669 |
rs113788539 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60196765 | AGGAGGTGGAGGTTG[C/T]GTTGAGCCGAGATTG | 84669 |
rs113801615 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60192593 | GCACGCATCACCACG[C/T]CCCGCTAATTTTTGT | 84669 |
rs113808627 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | USP32 | GRCh38.p7 | 17:60188247 | CCCAACAGGAGAGAA[A/C]TGTAAAGGATAAGAG | 84669 |
rs113809019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60181072 | AATTATTTCTAGAGA[C/T]GGGGCCAGGCTGGTC | 84669 |
rs113826022 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60327063 | GTAGCATGCTACAGC[A/C]CTATAGGGTGACTAT | 84669 |
rs113860838 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60234441 | TTTAAAAAAAAATTT[C/T]TTTGGACCGGGCGTG | 84669 |
rs113878940 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60192656 | GGCTGGTCTCCTGAT[C/G]TCAGGTGATCCACCC | 84669 |
rs113881007 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405116 | GCTGCAGTGACCCAC[A/G]ATCATGCCACTGCAC | 84669 |
rs113886698 | snp | A/T | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60263834 | TCAGTTAATAGGGCC[A/T]TTAACAATTTCTTCT | 84669 |
rs113906671 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378490 | TCAGACAGATATTTG[C/T]ACACCAATGTTCACA | 84669 |
rs113909630 | in-del | -/TTTGTTTG | 0.091965 | 0.196319 | intron-variant | USP32 | GRCh38.p7 | 17:60214955 | GAGACCCAAGTTCTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 84669 |
rs113926131 | snp | A/G | 0.0520825 | 0.152737 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264721 | AAAAAATCAGCCGGC[A/G]TGGTGGCACACACCT | 84669 |
rs113935624 | snp | C/T | 0.0170251 | 0.090679 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177048 | ACAGGCCACAGATGG[C/T]ACTGGTCTGTAGCCC | 84669 |
rs113937176 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377675 | TATAATTGACTCTTC[C/T]GTGTTTTCATCACAA | 84669 |
rs113943940 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264881 | AAAAAAAAAAAAAAA[A/G]AGAGAGAGAGAATAT | 84669 |
rs113962380 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60357591 | AAGGAATTGGGAGTT[A/G]TCAGCAAGAGATGTA | 84669 |
rs113975095 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60192518 | TGGCTCACTGGAACC[A/G]CTGCCTCCTGGGTTC | 84669 |
rs113982756 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60285476 | GAATTTGGGTGTCAA[A/G]TGCTATTTGTATCCA | 84669 |
rs113989413 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60379078 | CCTAGTAAGACATAG[C/T]TGAAAATATAATACT | 84669 |
rs114039484 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404813 | CTTAAATAGAAGGCT[G/T]GTCTTTTTACTTAAC | 84669 |
rs114077760 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60342327 | GGCACCTGCCTATAT[A/G]AGGTGTCTGTAGGCC | 84669 |
rs114080174 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409123 | GAGGCCGAGGTGCAC[A/G]GATCACCTGAGGCCA | 84669 |
rs114143662 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | USP32 | GRCh38.p7 | 17:60329392 | TGCTAGGTATGAGCC[C/T]AGACCATAAAATGTT | 84669 |
rs114148151 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60367140 | CCTAAGCCCACTTTT[C/G]AAAAGAATCTCACCT | 84669 |
rs114151449 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410281 | AACTGACTCAGTGCA[G/T]GAAGACAGCTTTGAC | 84669 |
rs114159398 | snp | A/G | 0.030665 | 0.119967 | intron-variant | USP32 | GRCh38.p7 | 17:60281819 | ATCTACATCAAAATC[A/G]CCCTGGAGGTCTGTA | 84669 |
rs114167832 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60355067 | AAACATAAAACTATG[A/G]TACATTCTTATTATA | 84669 |
rs114212653 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60245035 | TGCTCAAATATAGCT[C/T]CCCTTCTACTCTCAC | 84669 |
rs114223792 | snp | A/T | 0.0584853 | 0.160693 | intron-variant | USP32 | GRCh38.p7 | 17:60289766 | GCTACAACCTGAACT[A/T]TTTGATCAGGAAAAA | 84669 |
rs114265936 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60254178 | AAGTTAAATATTTGC[A/G]AATAACTATAAAAAT | 84669 |
rs114271481 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60357561 | TATGTAGATATATCA[A/G]TACATTCATAGTCAT | 84669 |
rs114293308 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60275064 | TAGAACATAAGCTTG[A/T]GGGCTGAGTTTCTGG | 84669 |
rs114298827 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60218115 | TTGCTATAATTACTA[C/T]GAAACACTACTGAAA | 84669 |
rs114327137 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60192467 | TGAGACGGAGTTTCG[C/G]TCTTGTTGCCCGGCT | 84669 |
rs114394505 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60337993 | TTTAATGCTTGAAAG[A/G]GAGTTTAGGATAAGA | 84669 |
rs114437248 | snp | A/T | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60243003 | AAGTTTTCAAATCCA[A/T]TTACGTACATTTTCT | 84669 |
rs114439504 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60349999 | CTCTGTGGTTTTTTC[A/G]TTGTTGTTGGTTTTT | 84669 |
rs114441917 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60287203 | GAGGGAGTCACACCC[A/G]TGAGCCAGTTAACGT | 84669 |
rs114480715 | snp | C/T | 0.021333 | 0.101051 | intron-variant | USP32 | GRCh38.p7 | 17:60352650 | CATGCACATTGGTGT[C/T]GATGCAATAAACAAG | 84669 |
rs114517815 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416350 | CCATCACATATACTA[A/G]GGGATGGAGGTAAAG | 84669 |
rs114527733 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP32 | GRCh38.p7 | 17:60268007 | GCCGAGACTATGTTT[C/T]GCCATGTTGGCCAGG | 84669 |
rs114551517 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | USP32 | GRCh38.p7 | 17:60391486 | GCTGTTAGGAACGAG[A/G]TTAGGATGTTATTTG | 84669 |
rs114598273 | snp | C/T | 0.029116 | 0.117091 | intron-variant | USP32 | GRCh38.p7 | 17:60298141 | ATTTAAATATTAAGT[C/T]TCCACCCCAAAGTAA | 84669 |
rs114598870 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | USP32 | GRCh38.p7 | 17:60294549 | TAGCACATAAATGGA[A/T]ACATCAATAAATATA | 84669 |
rs114613615 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403457 | TCATGCCACAGTCTG[C/T]CCTCGGGTTACAATT | 84669 |
rs114628997 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60194985 | ATAAACACTCAAGAA[A/G]TCGAGAACTATACAA | 84669 |
rs114636488 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60368169 | TTCCACCTAATCAAC[C/T]TCACCCTGTTTCATA | 84669 |
rs114641325 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405039 | AAAAATTAGCCGGTA[C/T]GGTGCTGCACAGCTA | 84669 |
rs114667540 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60262673 | TCCAATCCAGGTCTA[C/T]AGCCTTCAATATATG | 84669 |
rs114672378 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | USP32 | GRCh38.p7 | 17:60188815 | ATCTCTTTTGTCTAC[A/G]TGACTTTCTAAGCAC | 84669 |
rs114695649 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60281253 | ATTATAAAACACATG[C/T]TCTGGCCGGGTGCAG | 84669 |
rs114728992 | snp | C/T | 0.029116 | 0.117091 | intron-variant | USP32 | GRCh38.p7 | 17:60229407 | CAGAATTAATAACTA[C/T]TGCCCTAGTGAGGAT | 84669 |
rs114764221 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | USP32 | GRCh38.p7 | 17:60237215 | GTGCAATCTCAGCTC[A/G]CTGAAGCCTTGACCT | 84669 |
rs114772144 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60293199 | TATCAGCTAATACAT[C/G]TGCCTGCTATTGTGT | 84669 |
rs114803350 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60278555 | GTAAGACAGATAGTA[A/T]TAGGACAGAAAGACA | 84669 |
rs114806136 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60241794 | TATATAAAATTTGCA[A/G]ATATTTTCTCTAGGG | 84669 |
rs114880528 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408921 | TCAGATCATGCCTTC[G/T]GGCATCACCTCATTG | 84669 |
rs114927770 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305954 | ATTTGACAAATGATT[A/C]AGAGGAAGCCCCCAA | 84669 |
rs114933597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60242194 | TGTGATCACTGCATA[C/T]TCACACTAAAGCCGT | 84669 |
rs114941209 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60400365 | GGGAGACCAATTAGG[A/G]GGCGACTGCATTAAT | 84669 |
rs114944889 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60199253 | ATTTGTGAAACCTAG[C/T]AATTCTATTTTATAA | 84669 |
rs114953030 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | USP32 | GRCh38.p7 | 17:60187473 | TGCTTCAAAAGGAAA[C/T]GTGCTGCATCATCGT | 84669 |
rs114975069 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60352332 | CCAGCAGCCATTTTA[C/T]ACACCTATTTTTGAG | 84669 |
rs114977359 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60272497 | AACTAAACACAGGAA[C/T]CAAAGTGATCCTGTT | 84669 |
rs114978821 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60283803 | GAGGTTTCAGAAATA[C/T]CTCAAGAGCAGAAAA | 84669 |
rs114989781 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60398875 | GGTCCCAGCTACTTG[A/G]GAGGCTAAACTGGGG | 84669 |
rs115001162 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60230357 | TTCTGAAGAGCTCAG[A/T]CCATAGGTTAAATCT | 84669 |
rs115047082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60198940 | GCAATGTAGGGAGAC[C/T]CTATCTCTATAAAGA | 84669 |
rs115098783 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | USP32 | GRCh38.p7 | 17:60373814 | GCTCTTATAATAACC[C/T]TTACCTTAAAACACA | 84669 |
rs115122186 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60355762 | GATCACTAGCGCCTG[A/G]GAGGTCAAGGCTGCA | 84669 |
rs115134523 | snp | A/T | 0.029116 | 0.117091 | intron-variant | USP32 | GRCh38.p7 | 17:60244389 | TGTTCAATCTGTTTA[A/T]ATTTAAGGTAAAAAC | 84669 |
rs115136630 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60348596 | CCTAGGCAACATAGT[A/G]AGACCCTGTCTCTAC | 84669 |
rs115140437 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60422463 | GTGTTGGCGGTTGCC[A/G]TGGCTTTGCTCCGAG | 84669 |
rs115140667 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60391009 | GGACAGCGGTATCAG[A/C]GTGAGTGGTAGGGGG | 84669 |
rs115186291 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60387952 | TAGCTTCTGCACCAT[C/T]GTAAAGTTAAATTGT | 84669 |
rs115189846 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | USP32 | GRCh38.p7 | 17:60250870 | CAACATTTAAAAAAA[C/T]AGATTTTGCTTAATC | 84669 |
rs115195297 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | USP32 | GRCh38.p7 | 17:60282264 | ATTTAGCTAACCAAA[A/C]GTTTTAGAAGGAAGA | 84669 |
rs115272399 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60254116 | GACCTTCACAGTGGT[A/G]AAAGGAAAATAAAAT | 84669 |
rs115459353 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60293354 | TGTTTTGGACATCTA[C/T]GTCAAAAATCCAATC | 84669 |
rs115461269 | snp | A/G | 0.021333 | 0.101051 | intron-variant | USP32 | GRCh38.p7 | 17:60236707 | ATTTAAAACATTTCA[A/G]TTAATCCAAAAAGAC | 84669 |
rs115531896 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412366 | AAAAATTGGCCGGGT[A/G]TGTGATGTGAACCTG | 84669 |
rs115592943 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60242295 | ACTGTGCTCAGCTCC[C/T]CCTGGACCATTTTTT | 84669 |
rs115650131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60186636 | GGCCCCTAATACTCA[C/T]CCAAACCTTTGGGGT | 84669 |
rs115654059 | snp | C/G/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60257797 | GCCAGCTTTTTGGTG[C/G/T]TTTTTTTTTCCTTCA | 84669 |
rs115666893 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403569 | GTCCAGGGGGACTAA[C/G]GCTCCTCAGGTGTGG | 84669 |
rs115680583 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402777 | AGAGCTAATCTGTAC[A/G]CCATTTAGTGTCAGC | 84669 |
rs115710481 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60271815 | ATTTTTTTTCTTCTT[C/T]TTTTTTTTTTAAGAG | 84669 |
rs115721966 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60364542 | CCACCATGCCTGGCT[A/T]ATTTTTCTATTTTTA | 84669 |
rs115751951 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60283234 | ATATAAAAGTTCATG[A/G]TGTGGTCACGGTATA | 84669 |
rs115756040 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60314532 | TATCCAATCTGAAGT[A/G]CGGTGAAGAAAAAGA | 84669 |
rs115757694 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | USP32 | GRCh38.p7 | 17:60304368 | TATTTTTTTATTTTT[A/T]TTTTTTACGGAAACA | 84669 |
rs115798958 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405828 | TTAATAAATTCATCC[A/G]TAACCATCGTGCATA | 84669 |
rs115834539 | snp | C/T | 0.126564 | 0.217402 | intron-variant | USP32 | GRCh38.p7 | 17:60207364 | GAAGTGTGTTATATA[C/T]GACTGACTTCAGTTT | 84669 |
rs115839401 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | USP32 | GRCh38.p7 | 17:60329844 | ACCAACTCCTGCGAC[A/T]CAGTCTCCTTTTCTT | 84669 |
rs115876198 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411774 | GCTTATTTCACTTAG[G/T]AGAGTTTTTAAGATT | 84669 |
rs115932254 | snp | A/T | 0.0611083 | 0.163768 | intron-variant | USP32 | GRCh38.p7 | 17:60251285 | CACTTAAAAAAAAAA[A/T]AATAATAATAAATAA | 84669 |
rs115933168 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60192466 | TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCCGGC | 84669 |
rs115933675 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | USP32 | GRCh38.p7 | 17:60245734 | TGGATGTTAATAACC[A/G]TCTGGTGTCACTTAT | 84669 |
rs115984052 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412682 | GGGAGGGAGTGGGGT[A/G]CAAATACGGTGCCCT | 84669 |
rs115985602 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | USP32 | GRCh38.p7 | 17:60401951 | CTGAGACAAACTCTC[C/G]CCTAACTCTTATAGT | 84669 |
rs115986435 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60364360 | ACCTGCTAAGCCAAT[A/C]ATATTTATTTGGTTT | 84669 |
rs116011370 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60261993 | ATACTGACACCTGAG[C/T]AATAATTAACACACT | 84669 |
rs116013302 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60221390 | AAATTACATTAGTCT[A/G]TTTTATAACAGATTT | 84669 |
rs116015550 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60399501 | CTCTACAAAAAAATT[A/T]AAAAAAAAAAATTTA | 84669 |
rs116143833 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305443 | GGGGATCTGCCCCCA[A/T]GATCCAAACACCTCC | 84669 |
rs116195934 | snp | G/T | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60289001 | AGTAAACTGCATTTT[G/T]TTTTTTGTTTTTGTT | 84669 |
rs116217151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60230345 | TAATGCTTCTCATTC[C/T]GAAGAGCTCAGTCCA | 84669 |
rs116218857 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60392208 | CTCCTCCCTCTCCTT[C/T]CCTCCTCACGCCCTC | 84669 |
rs116255819 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405895 | TGCAGAAGCTCACTC[C/T]TGTAATCCAGCACTT | 84669 |
rs116271976 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60275794 | TTAGCTCACTGTAAC[G/T]TCTGCCTCCTAGGTT | 84669 |
rs116287261 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60240863 | GCAGGTGGCTGGCTC[A/G]TTTGCCTTACAGAAC | 84669 |
rs116288846 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233057 | AGCAAGAAGTAGTAA[A/T]TTATTCAAGGTCATA | 84669 |
rs116328627 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60353974 | CACAGAATGGATGTT[G/T]TCATTACCATGAGCA | 84669 |
rs116384169 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60361942 | GTATTACTATATGTG[A/G]GTATGTGCCTGGAAA | 84669 |
rs116413183 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60370501 | TGCAATGGCTCACAC[C/T]TGTAATCCCAACACT | 84669 |
rs116491640 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60195287 | TTCCTGAAATACTTC[A/C]TTCACTTAACTCCTG | 84669 |
rs116493380 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | USP32 | GRCh38.p7 | 17:60326608 | CCGGCCATGGTTTAT[C/T]TTCTCATTCTACTGG | 84669 |
rs116510075 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60361472 | TTTAGGCTGTTACCC[A/G]TCATGAAAAACCATA | 84669 |
rs116527161 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60226579 | CATGAATGTATATAA[A/T]TTTTTTATTATTAAA | 84669 |
rs116563086 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178019 | TTGTTCCAGTCTTGA[A/T]TAGAGAAAAAAATGA | 84669 |
rs116746247 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60331192 | TAAATAGTGTTAAGT[A/G]TTCTTCCTGAAAAAC | 84669 |
rs116747744 | snp | A/G/T | 0.0119091 | 0.0762411 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410799 | GAAATAGAAACTGTC[A/G/T]GCTGGGTGCGGTGGC | 84669 |
rs116764230 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60248855 | TTTCCTCGTATATGG[C/G]TCACATTTTCCTGTT | 84669 |
rs116799656 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60263101 | CTATAGACATGTGCT[A/G]CTGTGCCTGGCTACG | 84669 |
rs116801615 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393245 | GCTTATTTCACTTGG[C/T]ATCGTGCCTTCCAGG | 84669 |
rs116802718 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | USP32 | GRCh38.p7 | 17:60401444 | AGATCTTAGGAGCTT[C/T]ATTGGTTTTTGTCAG | 84669 |
rs116837619 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60286839 | ACTCAATGCTCACCA[A/T]CCTTCTTTGTTCTAA | 84669 |
rs116840198 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60281034 | GGTTCTTTGTTTTTA[C/T]AGATTATAAAATAAA | 84669 |
rs116859201 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | USP32 | GRCh38.p7 | 17:60254062 | ATTCTTTGTTTAAAA[G/T]GGTAGATCATGATAC | 84669 |
rs116897156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190511 | TAATAGTTACACTGG[A/T]GGAAATTTCTCATAT | 84669 |
rs116902251 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422793 | AAGAACTTTCATTCA[A/T]TCAGAAGTTTATGCA | 84669 |
rs116928133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423268 | ATGATCTTGGCCCAC[A/T]GCAACCTCTGCCCCC | 84669 |
rs116948275 | snp | A/G | 0.0379877 | 0.132479 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60392127 | ACCGCCTCCATGCCG[A/G]ATCACGTGACTCTTC | 84669 |
rs116975229 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393435 | GGAGAAACCAAATGG[A/G]GTGTATATGTACAGT | 84669 |
rs116983245 | snp | A/T | 0.106633 | 0.204807 | intron-variant | USP32 | GRCh38.p7 | 17:60210647 | ACTATCTTAGTTACG[A/T]TGAAAATGGATTGGA | 84669 |
rs117074095 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | USP32 | GRCh38.p7 | 17:60328127 | GGGCCAGGCTGCTAG[C/T]CCTGTGGACTGGAGT | 84669 |
rs117082737 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | USP32 | GRCh38.p7 | 17:60260496 | CTATTACACTCCAGC[C/G]TGGGTGACAAGAGCA | 84669 |
rs117112258 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60310815 | CCAAGGCAAGAGGAT[C/T]ACTTGAGCTCAAGAG | 84669 |
rs117154365 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60318004 | AAACAGAAAACAAAC[A/C]AACAAAAAAAACAGC | 84669 |
rs117178604 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60249022 | TTCCGGTACAGTATC[C/T]TGCAGTGTGAAGCTG | 84669 |
rs117198460 | snp | C/T | 0.0322114 | 0.122752 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378929 | GGTATGTTCTATATA[C/T]ATATATATTCACAAT | 84669 |
rs117213633 | snp | A/C | 0.0225045 | 0.103662 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393292 | ATGTGACTGACTCTC[A/C]CACTCCACCTCTCCA | 84669 |
rs117230595 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296516 | CCCCTACAGGTTTCA[A/G]AGAAAGCATGGCCCT | 84669 |
rs117264305 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | USP32 | GRCh38.p7 | 17:60350147 | CCTCCCAAGTAGGTG[A/G]GACCACAGGCTCCCA | 84669 |
rs117267778 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411630 | TCCTCCCACCTCAGC[C/G]TCCAGAGTAGCTGAG | 84669 |
rs117273931 | snp | A/G/T | 0.0182089 | 0.0937193 | intron-variant | USP32 | GRCh38.p7 | 17:60291052 | CTCTACAGAAGACAC[A/G/T]ATTATTATCCCCATT | 84669 |
rs117426739 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | USP32 | GRCh38.p7 | 17:60384637 | TCTCTACTGAAAATA[A/C]AAAATTAGTCGGGCA | 84669 |
rs117438032 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | USP32 | GRCh38.p7 | 17:60248955 | GGATTCTGAACCCCT[A/G]TGTGTTTTGTTTTGT | 84669 |
rs117491574 | snp | G/T | 0.106987 | 0.205054 | intron-variant | USP32 | GRCh38.p7 | 17:60247687 | TTTTGGTTTTTTTTT[G/T]GTTTGTTTGTTTTTG | 84669 |
rs117492812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337227 | GACTACTTCAGCATA[A/C]ATTCACCAGCACTAA | 84669 |
rs117516301 | snp | C/T | 0.0182019 | 0.0936463 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421987 | GGGATCTTTATACAC[C/T]CCCAAAACACACACA | 84669 |
rs117525554 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | USP32 | GRCh38.p7 | 17:60359593 | AGATGAGAGGATCAC[C/T]TGAGCCCAGGAGTTT | 84669 |
rs117606136 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | USP32 | GRCh38.p7 | 17:60187917 | AAGTAATAGTTTTCA[A/T]AGAAGACTATTGAAA | 84669 |
rs117611372 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | USP32 | GRCh38.p7 | 17:60182429 | TACATTTGTGAGAGA[A/G]TAAAAGTGAAAAGGC | 84669 |
rs117623174 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60290735 | GCTGCTAGATAGCCT[C/T]AGGATGGGGGCTGGC | 84669 |
rs117640420 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60325400 | TTCAGCCTGGGTGAC[A/T]GCGCAAGACCCTGTC | 84669 |
rs117659289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265738 | ATAGATTCTCATATA[C/T]GATTAAAAATTAAGA | 84669 |
rs117665140 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | USP32 | GRCh38.p7 | 17:60203564 | GATCTAGAAGCCTTG[C/T]TTTCCTTTATTTTAT | 84669 |
rs117677241 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60394251 | TCCGAGTTAGATTAT[C/T]GTAATTAATGGGAAG | 84669 |
rs117693502 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | USP32 | GRCh38.p7 | 17:60213951 | TTGTTTTTTGTTTTT[G/T]TTTTTTTTAAAGATG | 84669 |
rs117695334 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60351416 | TTCAACAAGCATTTA[C/T]GAAATGTCTACTATG | 84669 |
rs117703545 | snp | C/T | 0.0258936 | 0.110799 | intron-variant | USP32 | GRCh38.p7 | 17:60252340 | CCAATATATTTCAAG[C/T]ATGTGAAATTTCAAC | 84669 |
rs117732275 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | USP32 | GRCh38.p7 | 17:60326934 | AAAAAGTTGATCTCA[A/T]AGAAGTAGAGAGTAG | 84669 |
rs117768640 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP32 | GRCh38.p7 | 17:60276226 | TCAACTTTTTTGTAA[C/T]AAAATAAAAAATGTA | 84669 |
rs117789726 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | USP32 | GRCh38.p7 | 17:60254427 | AAACTTGGGCTGGGC[A/G]TGGTGGTTCACTCCT | 84669 |
rs117792986 | snp | C/T | 0.00636936 | 0.0560724 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60176897 | AGGCACAGTTCACAA[C/T]AGGGTTCGTTCTCCT | 84669 |
rs117808145 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60387653 | CTATGAATAGGCTTA[C/T]ATTCTTTGATACAAC | 84669 |
rs117879909 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60257053 | AATGGAGTTGATAAC[A/G]TTACCAAGCAAAGGA | 84669 |
rs117887047 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60327132 | ACGACCAGATTTTTT[A/G]ATGTTCCCAACACAA | 84669 |
rs117928432 | snp | C/T | 0.110167 | 0.207236 | intron-variant | USP32 | GRCh38.p7 | 17:60202009 | CTTTTATATGAGTAG[C/T]GTCAGGAATGTATTT | 84669 |
rs117959746 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60255625 | AAAAGTAATTTCTTC[C/T]TCTTTACTTTCCTAA | 84669 |
rs117989181 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60399661 | GAGCAAGACCCTGTC[A/T]AAATAAATAAATAAA | 84669 |
rs117992684 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60273210 | ACTCCTGGCCTCAAG[C/T]GATCTGTCTGCCTCG | 84669 |
rs118043345 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60262199 | TATGTATGTATGTAT[G/T]TATTTATTTGAGACA | 84669 |
rs118080663 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | USP32 | GRCh38.p7 | 17:60267970 | TGCCTGCCACTGCAC[C/T]CAGTTAATTTTTGTA | 84669 |
rs118095367 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | USP32 | GRCh38.p7 | 17:60320007 | CACCAAGGATGACTG[C/T]GTAAGTATCTTCAAT | 84669 |
rs118119096 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60291748 | CCATTTACAATGTTG[A/G]TTTTATACCAACTAG | 84669 |
rs118122258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259923 | ATATTTTTGTGACTA[A/G]AAATATGCTGTAGGA | 84669 |
rs118138720 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP32 | GRCh38.p7 | 17:60185319 | TCTCTGTATTCAACA[C/T]AAAAAGCTTGTACAG | 84669 |
rs118188487 | snp | A/G | 0.45843 | 0.138046 | intron-variant | USP32 | GRCh38.p7 | 17:60207830 | TATAGGCAGCCTTAC[A/G]TATTTCCCTTCTTCA | 84669 |
rs137876094 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60331911 | CTCAAAAAAAAATAA[A/C]ATAAACTTTAATATT | 84669 |
rs137876847 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | USP32 | GRCh38.p7 | 17:60205595 | GGGATGAATATTGGT[C/T]GGGGTAGGTCCCCAT | 84669 |
rs137880626 | in-del | -/A | | | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402244 | TTCCATCCCTCATTT[-/A]TCTTTTTTTTTTTTT | 84669 |
rs137882581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60239764 | TTGAGATGGAGTCTC[A/G]CTCTGTCACCCAGGC | 84669 |
rs137886376 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60400838 | CCAGCCTAGGCAACA[C/T]TGGTAGACCTAGTCT | 84669 |
rs137903463 | in-del | -/TCTGTGGCAGCAGCCAGTGTG | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60328862 | CCTGGAGCTACCTGC[-/TCTGTGGCAGCAGCCAGTGTG]TCTTGACTGCACACT | 84669 |
rs137903824 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60210646 | AACTATCTTAGTTAC[A/G]TTGAAAATGGATTGG | 84669 |
rs137916838 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | USP32 | GRCh38.p7 | 17:60197326 | AAATGATCTACAGGC[C/T]GGGTGTGGTGGCTCA | 84669 |
rs137922984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60336877 | TCAAACCAGTATCCT[C/G]CTGGTTGTTCTGTCA | 84669 |
rs137942340 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60285130 | CAGTCACACTCTTTT[C/T]GATATTAACAGAAAA | 84669 |
rs138068480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408789 | GCAAGCATGCAACGA[C/T]AGGGGGAATCTAAGT | 84669 |
rs138100138 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60181957 | TATAAGCAACAATGT[C/T]CTCAAAATGTAAAGT | 84669 |
rs138108299 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60291670 | CTACATGCAATCATC[A/G]ACACACTACTCAGAT | 84669 |
rs138165150 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP32 | GRCh38.p7 | 17:60394736 | ACTGTAGGTAATTTT[C/T]TATTTATTTATTTAT | 84669 |
rs138175986 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60252713 | AAAGCGAAAGGGGAA[C/G]ACATTACCTCAGGAA | 84669 |
rs138180427 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60340855 | CAGGAGCTCTTGTAA[C/G]GCAGGCCTGGTGGTG | 84669 |
rs138193471 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60345797 | GATCAGCCTGGACAA[C/T]GTGGCGAAACCCCAT | 84669 |
rs138199086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308534 | ATCCAAAAATTTACA[A/G]TCCACTCATCTTCAC | 84669 |
rs138206764 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414229 | TTAGCTAGGCATGGT[A/G]GCATAAGCCTGTAAT | 84669 |
rs138207619 | snp | C/T | 0.00494977 | 0.0495014 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205645 | TTCATTTGTAGATGG[C/T]GAAGAGGAGAAATCT | 84669 |
rs138209585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257693 | CTAGTTATGTTGCCC[A/T]GGCTGGTCTTGAACT | 84669 |
rs138220191 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | USP32 | GRCh38.p7 | 17:60380090 | GAAAGCTCCAAAGAA[A/G]GTAAGATTTAGGCAA | 84669 |
rs138223230 | snp | A/G/T | 0.024882 | 0.108992 | intron-variant | USP32 | GRCh38.p7 | 17:60212344 | ATGGTATAGGCTGTC[A/G/T]CTCCTTGGCTACAAA | 84669 |
rs138241938 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60297536 | TCACTGCAACCTCCA[C/T]CTCCTGGATTCAAGC | 84669 |
rs138260500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280547 | ACTATATATTTGTGT[A/G]TGAAAAAGTAATTAA | 84669 |
rs138274242 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60382662 | TTTTATATAACTCTG[C/T]ATAACACTTTAAGCA | 84669 |
rs138282980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183852 | CATCACACTGAATTG[C/T]AGTTACTGGTCTACA | 84669 |
rs138287544 | snp | C/T | 0.030278 | 0.119257 | intron-variant | USP32 | GRCh38.p7 | 17:60194260 | TGTTGTCCAGCCTGG[C/T]CTTAAACTCCTGGGC | 84669 |
rs138288421 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | USP32 | GRCh38.p7 | 17:60381619 | AGTCAGTCGTTTCAG[C/T]ATGGCAAGCCCTAGT | 84669 |
rs138288592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258343 | TGGGAAGCTCAACAA[C/T]GTATTTTAGAACATC | 84669 |
rs138309676 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60353245 | CATGTATGGATGCAA[C/G]GAGCAGGAAAGGCTC | 84669 |
rs138329623 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60262478 | ATTACAGGCGTGAGC[A/C]ACCATGCCCAACCTA | 84669 |
rs138389384 | in-del | -/C | 0.0158469 | 0.0875917 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409568 | TTAGTGGCTCTGAAA[-/C]CACCCTTGCAAAAAT | 84669 |
rs138440633 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60201086 | TGGTCTTAAACTCCT[A/G]GGCTCAAGCAATCGG | 84669 |
rs138468023 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60315095 | TCACACCTACAAGAA[A/C]GGCTATAATAAAATG | 84669 |
rs138502173 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422817 | TTATGCATGACCTGT[A/G]TTCCTGGCGAGATGA | 84669 |
rs138519242 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP32 | GRCh38.p7 | 17:60285801 | ATTAGGATTTAACAC[A/G]TAGAAGAAAAAGAGA | 84669 |
rs138519855 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60400057 | GCAACCTCCACCTCC[C/G]AGGTTCAAGCAATTT | 84669 |
rs138520671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229196 | AGGCATGCATCACCA[C/T]GCCCAACTAATTTTT | 84669 |
rs138524497 | snp | A/C | 0.0543475 | 0.155628 | intron-variant | USP32 | GRCh38.p7 | 17:60317973 | CTCGGCGACAGAGCC[A/C]GACTCCGTCTCAAGA | 84669 |
rs138532417 | in-del | -/T | 0.449218 | 0.151037 | intron-variant | USP32 | GRCh38.p7 | 17:60373444 | TTTAGCTTACTGTAA[-/T]TTTTTTTTTTTTTTT | 84669 |
rs138532685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60374844 | TGGGATCACAGTTGT[A/G]TATGCAGTCCATCGT | 84669 |
rs138545844 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232207 | AGATGGAGTCTCACT[C/G]TGTCATCCAGGATGG | 84669 |
rs138545882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60191801 | CGCGTGAGCCACCAC[A/G]CCTGGCCAATGCCTA | 84669 |
rs138554511 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60331420 | AAAAATACAAGTTAG[C/T]CAGGCATAGTGGCAT | 84669 |
rs138568290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60290869 | CATGATCGCTAGCGA[A/G]GATGTCTAGGGGTCA | 84669 |
rs138568519 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233264 | TGAGCCCAGGAGTTC[A/G]AGACTAGCCTGGCAG | 84669 |
rs138596888 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60238718 | CTGACACAGTAGAAT[C/T]GCTTGAACCCAGGAG | 84669 |
rs138623701 | snp | A/G | 1.65392e-05 | 0.00287564 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271463 | CGTTTCTCAAGATCA[A/G]TGATGTCTGATTCCT | 84669 |
rs138650393 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60244700 | GCAGGCGTTCCATCT[C/G]AGCTTACTGCAACCT | 84669 |
rs138660807 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60251750 | AAAGTAAATCCTTAA[A/G]CCAAGACATAGAGAT | 84669 |
rs138672235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337511 | ATAAATCAAATATTC[A/G]CTAAGTATATACAAT | 84669 |
rs138700863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60187863 | CTTCTTTTTCAAAGT[C/T]ACTTTAAAGCTCATC | 84669 |
rs138707769 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60376056 | TTTTTTTTAGTTTTT[A/G]TTTTTAGAGACGGGG | 84669 |
rs138712503 | snp | A/C | 3.29739e-05 | 0.00406028 | missense | USP32 | GRCh38.p7 | 17:60223480 | AGGGTTAAGGTGCAA[A/C]AAAATATTCCCATTG | 84669 |
rs138749078 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60365139 | TCATTATCAACTAAG[C/T]TCTATTCAGTTAATC | 84669 |
rs138751021 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | USP32 | GRCh38.p7 | 17:60401305 | AACCAGGGAGGCGGA[A/G]CTTGCAGTGAGCCGA | 84669 |
rs138774223 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60268818 | ATATTGAACACCACA[C/T]CCAAAATATGCAACA | 84669 |
rs138812926 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60292096 | CACTAGACCTTCCAG[G/T]GTATTTGACATAGTT | 84669 |
rs138819857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60352428 | ATGACCATGGAACTG[C/T]CATATGACCCTTGGA | 84669 |
rs138840563 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60303416 | TGCCTAAAACTGAGA[A/C]AGAAATAGGACTACA | 84669 |
rs138844900 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60253638 | GGGGGTGGTGGCACA[C/T]GCCTGTAATCCCAGC | 84669 |
rs138849671 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60215124 | AGGTGCACGCCACCA[C/T]ATCTGGCTAATTTTT | 84669 |
rs138868289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60218795 | GTAGAGACAGGGTTC[A/G]TGTTGGCCAGGCTGG | 84669 |
rs138883562 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60323429 | CTATATAGACAGAAA[G/T]TAGATTAGTATATTA | 84669 |
rs138891010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232826 | TGCTGGGATAATAGG[C/T]GTGAGCCACCATGCC | 84669 |
rs138893088 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423021 | TCCCTCCCCCTGGCC[C/T]TTCCCTTCAGAGTGG | 84669 |
rs138901306 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60297345 | TCAAGGCTGCAGTGA[A/G]CTATCTTGCCACTGT | 84669 |
rs138902101 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | USP32 | GRCh38.p7 | 17:60307959 | GGCACTGGCAGATGC[C/T]GGCAGGCCACTGACC | 84669 |
rs138904415 | in-del | -/AT | 0.247621 | 0.249989 | intron-variant | USP32 | GRCh38.p7 | 17:60324283 | TATATATATATATAT[-/AT]TTTAATTAAAAACTA | 84669 |
rs139004365 | snp | A/G | 0.000280642 | 0.0118424 | synonymous-codon | USP32 | GRCh38.p7 | 17:60192927 | ATAGCCCATACTGTC[A/G]TCACTGAAACAGAAG | 84669 |
rs139039180 | snp | C/G | 9.88403e-05 | 0.00702925 | missense, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179339 | CTTTTTGCCATCAGT[C/G]TTTGGCAGAAATTGT | 84669 |
rs139042899 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | USP32 | GRCh38.p7 | 17:60365734 | TAAAAGAATGCATTA[A/C]GATAAACCATTTTTA | 84669 |
rs139070104 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | USP32 | GRCh38.p7 | 17:60315266 | TTAGCCAGGCGTGGC[A/G]GTGTGCGCCTGTAGT | 84669 |
rs139078853 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60276845 | AAAACATCCTTTAGT[A/G]CTGACGTTTAAGTGT | 84669 |
rs139079481 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | USP32 | GRCh38.p7 | 17:60225325 | GGCTGGGCATGGTGG[C/T]GCGTGCCTGTAGTCC | 84669 |
rs139085176 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60348100 | GCACTCCAGCCTGGG[C/T]AACAGAGCGAGACCC | 84669 |
rs139153803 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60282285 | AGAAGGAAGACCTTA[A/G]AACTTTGCAACTTTC | 84669 |
rs139157689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60386011 | AAATTCTATTCTATT[A/G]CTGCATAACACACAC | 84669 |
rs139169562 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60341191 | TTGTGGTGTTCTCTG[C/T]TCCTGAATTTGAATG | 84669 |
rs139174970 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60230998 | TTCAAAATTATCCTA[G/T]AACCCTGGTTTTCAG | 84669 |
rs139224337 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60272154 | TCTTGGATTTAAAGT[C/T]TCTATGTACAGCTTC | 84669 |
rs139233301 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407169 | GCACAGATTGGAGTT[C/T]ATGGAACCTGAGGCA | 84669 |
rs139233366 | snp | A/T | 0.000153988 | 0.00877328 | missense | USP32 | GRCh38.p7 | 17:60209519 | GAAACCCATTAAACC[A/T]GGGAGCATATTTTGC | 84669 |
rs139251858 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394100 | TTTAAGACCTCAGAT[A/T]AGCTGCATTACTGAA | 84669 |
rs139262282 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60287871 | ATAATTCCAGCACTT[C/T]GGGAGGCCGAGGCGT | 84669 |
rs139318435 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60364441 | CTAGAGTGCGGTGGC[A/G]CGATGTCCACTCACC | 84669 |
rs139318680 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60276032 | AGATTGTAATCGCCT[C/G]ATGGGTCAATGTTTG | 84669 |
rs139327262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402687 | CATAAGAAATTATTC[C/T]AAACACTGAGTAGCA | 84669 |
rs139355198 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60223856 | CATAATGAGAATTAT[A/G]TGTCCTCCGACTGGA | 84669 |
rs139357149 | snp | A/T | 0.084364 | 0.187256 | intron-variant | USP32 | GRCh38.p7 | 17:60280110 | ATTATTATTATTATT[A/T]TTTGAGATGGAGTTT | 84669 |
rs139396841 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266221 | TCTGGAACAGTTCTC[A/T]TCTGTAATAAACTAT | 84669 |
rs139425883 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60339206 | ATGAGCCACCGCGCC[C/T]AGCCTAGAAGAACAT | 84669 |
rs139451251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60193174 | CCAGATGTCTCTAAG[A/G]GAGTCCATGTGGCCC | 84669 |
rs139460054 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60324744 | ATGGTGGCTCACATC[C/T]GTAATCCCAGCATTT | 84669 |
rs139462812 | in-del | -/T | 0.0433465 | 0.140692 | intron-variant | USP32 | GRCh38.p7 | 17:60221330 | CCCTGGAGCTTGAGG[-/T]TATTTTTCATAAACG | 84669 |
rs139463463 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60277842 | TACAAGACAGAATAG[-/AT]ATATGTTTTCTTCCA | 84669 |
rs139470955 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60319836 | ATAACAACTATTCAC[A/G]TAGTATTTACATTGC | 84669 |
rs139475411 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60311721 | TCCCAGCTACTCAGG[A/G]GGCTGAGGCAGAAGA | 84669 |
rs139490342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60273459 | AAGGCTACTCTAAAC[G/T]TGTCCCAACAAAGCT | 84669 |
rs139499854 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60254226 | CTTTAAAAATCAGAG[C/T]GAGGGAATTAGTTTA | 84669 |
rs139506357 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60359454 | CTCTTGTCCAAGGCC[-/T]TATGCTTATTACTAA | 84669 |
rs139515401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60259766 | TCACCACTATGACTG[C/T]TGCTGTCACTCACTA | 84669 |
rs139539403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60342995 | ATGCAGAAATCATCC[A/G]TCTTCTGCATCGATC | 84669 |
rs139543169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60384234 | AGATCCTTTTCATAA[C/T]GTAATCTCTCCAGAC | 84669 |
rs139560058 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60234264 | GACCATAGGCGCCTG[A/C]CACCATGCCCGGCTA | 84669 |
rs139579069 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60325543 | TGTGATATAATTTCA[C/T]TGGATTTTGTCAGGG | 84669 |
rs139605763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60266748 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTC | 84669 |
rs139606525 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60194831 | CTAATGATTCTTTCA[C/T]CCAAGAGAAACCTCC | 84669 |
rs139623259 | in-del | -/AC | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60356477 | CATTTGAACACACAC[-/AC]CCGAGTAGTATAGAA | 84669 |
rs139643828 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60245977 | CGTAATGATCAAATA[C/T]GGTAATTAGGATATT | 84669 |
rs139646955 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | USP32 | GRCh38.p7 | 17:60366415 | ACCTGCCTCGGCCTC[A/C]CAAAGTGCTGGGATT | 84669 |
rs139685416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60241158 | GTGCGCCACCATGGC[C/T]GGCTAATTTTTTGTA | 84669 |
rs139716093 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415091 | TATTTTCATGCTTGG[A/G]GAGGGTGGTATCCAG | 84669 |
rs139735771 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60298772 | CTGGGTTTATGGATA[C/T]ATTCATTATCTTGAT | 84669 |
rs139767693 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420975 | TTCCAAATTGTCACT[A/G]TTGTAACAGTCCTCA | 84669 |
rs139770283 | in-del | -/AC | 0.266819 | 0.249434 | intron-variant | USP32 | GRCh38.p7 | 17:60260715 | GATAGAAAATTATAT[-/AC]AGATTTAGGAAAATT | 84669 |
rs139782998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60247856 | ACCTGGATAATTGTT[C/T]TGTATTTTTAGTAGA | 84669 |
rs139824249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60375199 | TCTCTGTGGATACCA[C/T]GCTTCTTCTTACCCT | 84669 |
rs139834899 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60316251 | TAACATTTCATTCTC[-/A]AAAAAAAAAAAAAAT | 84669 |
rs139849460 | in-del | -/GAGAGAG | | | intron-variant | USP32 | GRCh38.p7 | 17:60355847 | AAAAAAAAAAAAAAA[-/GAGAGAG]AAAGAAAAAAAAAAA | 84669 |
rs139898713 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393036 | TTAAGAACATTGATA[C/T]TGTTTTGCATCCATT | 84669 |
rs139929562 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60235043 | CAACAATAAACCAGG[C/T]TCATGTTCTTGTCAG | 84669 |
rs139948167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60278367 | ATCTAGTGTGGAAAG[C/T]ACAATGAAAAAATAG | 84669 |
rs139964086 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410484 | CCATCTTGGCTAACA[C/T]GGTGAAACCCTGTCT | 84669 |
rs139993416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60226562 | CCTTATTTCCCATAG[C/T]ACATGAATGTATATA | 84669 |
rs139997177 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60370531 | TTTGGGAGGCCGAGG[C/T]GGGAGGATCACTTGA | 84669 |
rs140014385 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60212863 | GGCTTGACTGATTCT[C/T]GTGCCTCAGCTTCCT | 84669 |
rs140025044 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | USP32 | GRCh38.p7 | 17:60240745 | TGTACAGTGTGCTTT[A/T]GGGTACTTTAATTTC | 84669 |
rs140053785 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60340539 | AGATCTTTCTCCATC[C/G]CTTTATTTTGAGCCT | 84669 |
rs140063471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60224623 | CTCGTCTCTACAAAA[A/C]AATTAAAAAATTAGC | 84669 |
rs140093957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60290881 | CGAAGATGTCTAGGG[A/G]TCAGTTTTGTGGAAC | 84669 |
rs140157108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60189385 | GTCAGTTACCGTTAC[C/T]AACTTATCCAAAGGG | 84669 |
rs140157858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254626 | ATGACCTGAGTCTGC[A/G]CAGTCAAGGCTGCAG | 84669 |
rs140162592 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60342364 | CAGAAGTGTTTCCCA[G/T]TTAGGCTACACAGGG | 84669 |
rs140202875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258737 | TGTTTACAGGACATT[C/T]CAAAATGAAATGACT | 84669 |
rs140203689 | snp | A/C/G | 0.02016 | 0.0983543 | intron-variant | USP32 | GRCh38.p7 | 17:60207451 | ATTAAGAAACTGTCA[A/C/G]TGAGGTGAGAGTGTG | 84669 |
rs140207573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60346355 | CAGGTAAGCTAAATG[A/C]CACTGGATTCTGGCA | 84669 |
rs140222871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60300794 | TATGTAATTCCAGAA[C/T]ATTTTCGCCAACCCA | 84669 |
rs140243015 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60214037 | AACCTCTGCCTCTGG[G/T]TTCAAGCAATTCTCC | 84669 |
rs140298337 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60355324 | AACTTTCATAGGTGA[C/T]AGAAATGTTCTGTAT | 84669 |
rs140314036 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419460 | CTGTGCAACAGGCTG[A/G]GCACGGTGGCTCATG | 84669 |
rs140333093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60188041 | GCTGGAGTGCACTGG[C/T]GAGATCACAGCTCAC | 84669 |
rs140352529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315485 | ATCTATACACTGTTG[A/G]TGGAAATGTAAAAGG | 84669 |
rs140358274 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60267253 | GCTACTAAAAATACA[A/G]AAAATTAGCTGGGCG | 84669 |
rs140376997 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60389546 | AGACTCTGTCTCGAG[-/A]AAAAAAAAAGCTTCA | 84669 |
rs140378781 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423590 | TGCCCCAGCCTCCCA[A/G]GTAGATGGGATTACA | 84669 |
rs140382321 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60355798 | CCATGATCATGCCAC[C/T]GCACTCCAGGCTGAG | 84669 |
rs140418995 | snp | A/G | 0.077417 | 0.180873 | intron-variant | USP32 | GRCh38.p7 | 17:60218170 | TGGATGGATCACGAG[A/G]TCAGGAGATAGAGAC | 84669 |
rs140441164 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | USP32 | GRCh38.p7 | 17:60220978 | GAAAACAGAAACTCT[A/G]TACAGAGTCTTTTAA | 84669 |
rs140449325 | snp | A/G | 0.00138381 | 0.0262676 | missense | USP32 | GRCh38.p7 | 17:60205646 | TCATTTGTAGATGGC[A/G]AAGAGGAGAAATCTA | 84669 |
rs140451644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60310963 | TAGATCTCATGAAGA[C/T]GAGAGTAGATTGGTG | 84669 |
rs140453793 | snp | G/T | 0.104504 | 0.2033 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393762 | CGATCTCGACTCACC[G/T]CAACCTCTGCCTCTC | 84669 |
rs140458697 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60321081 | AGAGGACTGAAAATC[A/G]GAGATCCAGGGAAAT | 84669 |
rs140463372 | snp | A/C | 0.000402185 | 0.014175 | missense | USP32 | GRCh38.p7 | 17:60183179 | CCTTTCGGGCTGCTG[A/C]TGATGTTAGCGCTGA | 84669 |
rs140478456 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60274898 | TCCTTCAGATCTTTA[C/T]TCAAATGTCACATTC | 84669 |
rs140514528 | in-del | -/A | 0.0755793 | 0.179102 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306642 | ACTCCGTCTCGAAAG[-/A]AAAAAAAAAATGTCT | 84669 |
rs140528683 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60357681 | TTAATATCATTAAAC[A/G]TTCTCAGGCTGAAGC | 84669 |
rs140544951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422741 | AGAAGAGAAGAACAA[C/T]GATAGGGTACCTGAG | 84669 |
rs140545507 | snp | C/T | 0.000610033 | 0.0174541 | missense, utr-variant-5-prime, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266080 | GGTCAACATCAAATA[C/T]CTTGAAGCAAACTAA | 84669 |
rs140561773 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60238600 | CTGAGGTCAGGAGTT[C/T]GAGACCTGCCTGACT | 84669 |
rs140593236 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60363182 | TTTTGAGGCCAGGCG[C/T]GGTGGCTCACACCTG | 84669 |
rs140629289 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60312975 | GTGGCTGGGCACGGT[A/G]GCTCATGCCTGTAAT | 84669 |
rs140636604 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60222744 | TGGAGTACAGTGGCG[C/T]GATCTTCGCTTGCTG | 84669 |
rs140675254 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60294420 | TGTGTATTACTGTGT[C/T]AGTGTGAGTATATAG | 84669 |
rs140694577 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60242446 | CAGGCAGAGTCTCAC[C/T]GTCACCCAGGCTGGG | 84669 |
rs140735257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402847 | GCTTTCTCACTCATG[C/T]CTGCCAGTTGATGCT | 84669 |
rs140773142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60338837 | CCCTCAAATTCTGTT[C/T]ATTATTTTATTCAAG | 84669 |
rs140773193 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60283045 | TATAAAGTGTTGCAG[A/C]AATGCAAATAGTAAA | 84669 |
rs140801872 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60255456 | GTGCCCGCCACCATG[A/C]CTGGCTAAGTTTTTG | 84669 |
rs140812576 | in-del | -/A | 0.316968 | 0.240864 | intron-variant | USP32 | GRCh38.p7 | 17:60386191 | ATGCAGAAAGACATT[-/A]AACTGCTCAACTTAA | 84669 |
rs140836005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404136 | TCCCTTGAGCTTGGG[C/T]GGAACTGTATGACTG | 84669 |
rs140880223 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411999 | ATAATTTAATATTTA[A/G]TAATGCTTCTGTTTA | 84669 |
rs140896998 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60260584 | ACTATGCAGAGGATA[A/C]AAAGACTAAGTTAAT | 84669 |
rs140902555 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407927 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 84669 |
rs140905334 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60187666 | TGTGGAACACAGGCT[A/G]CAGTGCTAGATGAAG | 84669 |
rs140926140 | in-del | -/T | 0.0995161 | 0.199636 | intron-variant | USP32 | GRCh38.p7 | 17:60247687 | GTTTGTTTGTTTTGG[-/T]TTTTTTTTTGTTTGT | 84669 |
rs140938184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60290739 | CTAGATAGCCTCAGG[A/T]TGGGGGCTGGCCACT | 84669 |
rs140967842 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60357270 | AGCCTGGGCAACAGA[A/G]GGAGACCCCATCTCT | 84669 |
rs140985609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60316482 | AGTGAGCACGTTTCC[A/G]CAGTTCAACTAGTAA | 84669 |
rs140993473 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | USP32 | GRCh38.p7 | 17:60220736 | GCAAGCTCTGCCTCC[C/T]GGGTTCTTGCCATTC | 84669 |
rs140999599 | in-del | -/TGTG | | | intron-variant | USP32 | GRCh38.p7 | 17:60291538 | CTCTCTGTGTGTGTA[-/TGTG]TGTGTGTGTGTGTGT | 84669 |
rs141020011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403462 | CCACAGTCTGCCCTC[A/G]GGTTACAATTCAGAT | 84669 |
rs141029275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60274339 | CAAACATACATACAA[C/T]TGGGATCCCAGAAAG | 84669 |
rs141035473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362565 | ATCTGTTGTATACTT[A/C]AACGCTGCAGGAGAG | 84669 |
rs141053396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60374543 | GCTAGGACCACAGGC[A/G]TGTGCCTAATTTTTG | 84669 |
rs141055799 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60284972 | TAAATCCCCACTTGT[C/T]GTTGTTATATTGAGA | 84669 |
rs141067102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60222233 | CCTTGCCTTTATTTA[C/T]GAATGAATGAACGAA | 84669 |
rs141105409 | in-del | -/TAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60180868 | TATAATTGTAATTAC[-/TAT]TATTATTATTATTAT | 84669 |
rs141126106 | snp | C/G | 0.000307953 | 0.0124049 | missense, intron-variant | USP32 | GRCh38.p7 | 17:60288559 | TTTGGTAGAAAGTAG[C/G]AGTATCACTATCATC | 84669 |
rs141140280 | in-del | -/G | 0.0154538 | 0.0865337 | intron-variant | USP32 | GRCh38.p7 | 17:60269240 | ACTCCATTGTTAATA[-/G]CAAATATCCCAAACT | 84669 |
rs141145808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256394 | TCAAAAAATTGTCCT[A/G]TTCACTTACAGCAGA | 84669 |
rs141167976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60394625 | TGGTGCAAATATCAT[A/C]GATTACTTACACAAA | 84669 |
rs141203044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60276515 | AGTAGTAGATCAGCA[C/T]ACAAAAAAATCTAAC | 84669 |
rs141203672 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60187285 | GCACTGCATAACTAT[C/G]CAGGCTAAAGAGCTC | 84669 |
rs141223408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60225173 | AAATAGTGAAAATAG[C/T]CGCATGTGATGGCTC | 84669 |
rs141274536 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402508 | CCTCTTTGGCCTCCC[A/T]AAGTGCTGGGATTAC | 84669 |
rs141282387 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60332695 | CTATGCTTTCCCTTT[A/T]CTCCTGCACCAATAT | 84669 |
rs141285121 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60351751 | TTTATTAAATGTCTA[C/T]TTATCTCAGTCAAGA | 84669 |
rs141289721 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60396993 | CTTCCTAAGCTCCTG[-/A]AAAAATCAAGTAGCA | 84669 |
rs141297386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387154 | GTGTATAGAATGATA[C/T]ATTATGCTAAACGAA | 84669 |
rs141306183 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412488 | TTCAGTGAGCTATGA[C/T]TGCACCACTGCACTC | 84669 |
rs141312789 | snp | A/C | 0.000153988 | 0.00877328 | missense | USP32 | GRCh38.p7 | 17:60211404 | AAAGATGTCTCCCTG[A/C]GATAAAATACTGTGT | 84669 |
rs141324652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60282137 | TTCAATGACTACCAC[A/G]GAAATCAATGCGCAC | 84669 |
rs141346475 | snp | C/T | 4.94279e-05 | 0.00497107 | missense | USP32 | GRCh38.p7 | 17:60190652 | TGAAAGCTCTGTCTT[C/T]CCCACAATCAATTTT | 84669 |
rs141356612 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60201117 | CCCACCTCAGCCTCC[C/G]AAAATGCTGAGATTA | 84669 |
rs141371172 | in-del | -/C | 0.277334 | 0.248501 | intron-variant | USP32 | GRCh38.p7 | 17:60330518 | TTTCTCTCTCTCTCT[-/C]CCCCCCTCCCTCCTT | 84669 |
rs141376143 | snp | A/G | 0.077417 | 0.180873 | intron-variant | USP32 | GRCh38.p7 | 17:60202974 | AGGGATTGCAGTTAT[A/G]CAGTCACAAGCCAAA | 84669 |
rs141431934 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60302129 | TTTATTTATTTATTT[A/G]TTTATTTATTTATTT | 84669 |
rs141470616 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60252675 | ATCTCTAGGTAAGAA[A/G]GGAAGAGAAAGGGAA | 84669 |
rs141470683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60307041 | ATTGAAGAGGACACA[C/T]ACACAAAATGGAAAG | 84669 |
rs141481291 | in-del | -/TTTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60302114 | TAAATATTTTGTTTG[-/TTTA]TTTATTTATTTATTT | 84669 |
rs141486526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258137 | AACCTGAGGGACTCT[G/T]AAGTTGAGCTCCAAC | 84669 |
rs141534752 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60233702 | TTCTAATTAAAACAT[A/G]TTCAGAGGATTGTTA | 84669 |
rs141563795 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231759 | TCAAAAAGGAAGATA[C/T]ACATTATGTAATGTA | 84669 |
rs141575581 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | USP32 | GRCh38.p7 | 17:60314777 | ACAAAACCAAACAAA[G/T]GTATATAATACATTC | 84669 |
rs141589287 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60189288 | AGCCTTGGTGTGTGC[A/G]GCATATTTTGGGATC | 84669 |
rs141596145 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264391 | GGCATGGTGGTGCAC[A/G]CCTATAGTCTCAGCT | 84669 |
rs141622337 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60201661 | TAGTGTCGTTGATCA[C/T]TTTTTTTTTTTTTTT | 84669 |
rs141626267 | snp | C/T | 0.030278 | 0.119257 | intron-variant | USP32 | GRCh38.p7 | 17:60238790 | GCCTGGGCAACAGAG[C/T]GAGACTCCATCTCAA | 84669 |
rs141641824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244551 | ATGCCTTTTTAAATA[A/C]AACTATTTTGGGGGA | 84669 |
rs141648875 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60369646 | ACACATTAAAAGTAG[C/G]AATACAAAACAAATA | 84669 |
rs141665170 | snp | C/T | 3.46266e-05 | 0.00416078 | missense | USP32 | GRCh38.p7 | 17:60181673 | CTCCTCCCCAAAGTC[C/T]GTGGGCTGCTATTAG | 84669 |
rs141665670 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | USP32 | GRCh38.p7 | 17:60197025 | GTCTCTACTAAAAAT[A/G]CAAAAATTAGCTGGG | 84669 |
rs141670319 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60319022 | ATATGATACCACTTA[C/G/T]GTAAAGTAATTTGAA | 84669 |
rs141677707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229694 | CACTTTAGTTTTGCT[A/C]TAAGTGATCTTAAAT | 84669 |
rs141690406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60195258 | CTGTAGCATTTGAAA[C/T]GACTATCACTCCTTT | 84669 |
rs141720689 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405684 | GGAGGATCACCTGAG[C/G]CTGGGGAGGTGGAGG | 84669 |
rs141734673 | snp | A/T | 9.88419e-05 | 0.00702931 | missense | USP32 | GRCh38.p7 | 17:60345506 | TTTGGAGGCACTCCA[A/T]CCCCAAGCACTTCCC | 84669 |
rs141739810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286220 | TAGAAATTAACACTT[A/C]GGCCTGTGTAGTGAA | 84669 |
rs141799474 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60386603 | TCACAATCCCAACTC[-/T]TAACTTCCTTACACA | 84669 |
rs141822323 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60309046 | ACTAGAAAAAAACAT[C/T]GGGGGAAATGCTCCA | 84669 |
rs141823674 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410001 | CAAAACTAACAATCT[C/T]CTTGTTCAGCGACTA | 84669 |
rs141832425 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60367231 | AAATATTCAGAGGTC[A/G]GGAGTGGTTGCTCAA | 84669 |
rs141832443 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403260 | TGACCTCGTGATCTG[C/T]CGGCCTCGGCCTCCC | 84669 |
rs141841872 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60370591 | CATGGCAAAACCCTG[A/C]CTCTACAAAAAAAAA | 84669 |
rs141851529 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60184060 | GGGAGGCCAAGGCGG[A/G]TGGCTCATGAGGTCA | 84669 |
rs141886077 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60228983 | AATTAGGTTTCAAAA[G/T]AAAATTTTCCATAAA | 84669 |
rs141897832 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60373532 | CACTGCAACCTGCAC[C/T]TCCTGGGTTCAAGCA | 84669 |
rs141911023 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60352543 | TTAAACCTAACTGAT[A/G]AAGGTATCAGGTACA | 84669 |
rs141916071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416548 | GACTTGATTTGCCCT[A/G]TAGAGTCATTTTATG | 84669 |
rs141964471 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60303813 | TTTGGAATGGCTCAA[A/G]AATAAACTCAACAGA | 84669 |
rs141975764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214981 | TGTTTGTTTGTTTGT[C/T]TTTAATAGATGGAGT | 84669 |
rs141981646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301346 | GTTACAATTTTTCCA[C/T]ATCTTCCTCAACACT | 84669 |
rs142000207 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60219020 | TTTTGCATGTTATAC[A/G]TTAAAATGGGAACTA | 84669 |
rs142000332 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178276 | CATGTGTTCTCTCTT[C/T]TTTAAAGTGCAAGAC | 84669 |
rs142003903 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422873 | TGGTTATGAAGACTT[G/T]AGAGTATGTGTATGT | 84669 |
rs142007289 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60359281 | ACAGCTTATATTGTA[C/T]GTTTATTGAATTGTA | 84669 |
rs142026337 | snp | A/C | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60220375 | ATTTTTTGTACTAGT[A/C]GTGAGGATGCAACTG | 84669 |
rs142037093 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60308096 | TCCAGCTGCTGAGAG[C/G]TACTTCTACCATTCA | 84669 |
rs142046029 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60267230 | GGTCAACATGGTGAA[A/G]TCCCGTCGCTACTAA | 84669 |
rs142119436 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | USP32 | GRCh38.p7 | 17:60380472 | GCTAGGGAAGCTGAA[A/G]TAGGAGGATGGCTTG | 84669 |
rs142238740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60346791 | TTTTAAAGGCTAAAC[C/T]AAGCAAAATGAACAA | 84669 |
rs142238919 | snp | C/G | 0.104859 | 0.203554 | intron-variant | USP32 | GRCh38.p7 | 17:60190124 | ACTTAGTTTCCAAGA[C/G]AGCGGGCTGTTAGAA | 84669 |
rs142256076 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414776 | TTCATCAAGTTGCTC[A/G]TTTACTTCTCCAGGC | 84669 |
rs142258820 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60369423 | AGCAAGACCCCTACC[A/T]AAAAAAAAAAAAAAA | 84669 |
rs142276303 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60247462 | TGGGATTACAGGCAT[A/G]AGCCACCTCGCCCAG | 84669 |
rs142287056 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60373343 | AGCCCTAGGACATTA[C/T]CATGGAGTACTGCAG | 84669 |
rs142307882 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296182 | AGCTAGGTGGAGGTA[C/T]GTATTAGATATATGT | 84669 |
rs142310202 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60348946 | GTACTTTATTTAAAA[C/T]TGGATTTATAATATT | 84669 |
rs142317905 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | USP32 | GRCh38.p7 | 17:60332155 | CCCAGATACTCGGGA[A/G]GCTGAGGCACGAGAC | 84669 |
rs142320839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60398687 | GTTGCTTAGCTAGGT[A/G]CAGTGGCTGGCTCAG | 84669 |
rs142330691 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP32 | GRCh38.p7 | 17:60320857 | CACATGCAGGTTCCA[A/G]GAACTAGGACCTGGA | 84669 |
rs142335014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60195499 | CGTACCACCATGCCC[A/G]GCTAATTTTTGCATT | 84669 |
rs142358232 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60281475 | CTCGGAGGATGGAGG[G/T]TGCAGTGAGCTGAGA | 84669 |
rs142372395 | snp | C/T | 0.00335509 | 0.0408202 | synonymous-codon | USP32 | GRCh38.p7 | 17:60198331 | TACTTGAATCCAAAC[C/T]GCATCATATAGGTCT | 84669 |
rs142389140 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306363 | AATTTTCTGGCCGGG[C/T]GCAGTGGCTCATGCC | 84669 |
rs142403251 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60200072 | GGTGGCAGGCACCTG[C/T]AGTCCCAGCTACTCG | 84669 |
rs142448957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60285556 | GATAGGATAATACTG[C/T]AGACCCCCTCTGCCG | 84669 |
rs142493530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60221725 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 84669 |
rs142554721 | in-del | -/G | 0.0770498 | 0.180522 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403652 | AATGAGTTTATTTAA[-/G]GAAAGGGGGTCGTGA | 84669 |
rs142567502 | snp | C/G | 0.0325976 | 0.123435 | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419279 | CAGAAAACCAAATAC[C/G]GCATGTTCTCACTTA | 84669 |
rs142634334 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60323080 | AGCCACTTTGGAAAA[C/T]AGTCTGGCAGTTCCT | 84669 |
rs142634698 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394033 | AAACCAGATCAGCAG[C/T]GTGGCATTAGTCACA | 84669 |
rs142645250 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60325182 | ATTTTGGGAGCCTGA[A/G]GAGGGCAGATCACTT | 84669 |
rs142660066 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60275228 | TTGGGAGGCCAGGGC[A/G]GGCGGATCACCTGAG | 84669 |
rs142660599 | snp | C/T | 0.000184504 | 0.00960301 | synonymous-codon | USP32 | GRCh38.p7 | 17:60208742 | ACTTATATGCCCACA[C/T]GTCTTGCATTTTACT | 84669 |
rs142661032 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60329054 | AAGGCGCCACCAGCC[A/G]CACGTTTCTGGCCAG | 84669 |
rs142684839 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60233873 | TTGAATAAATTCCCA[C/T]ACTCTGCCTCCTTTC | 84669 |
rs142695090 | in-del | -/ATT | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419818 | TCAAGGTTAAAAAAA[-/ATT]ATTATTATTATTATT | 84669 |
rs142722432 | in-del | -/TAATAATAAT | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60279843 | GCCTGTCTCAAATAA[-/TAATAATAAT]TAATAATAATAATAA | 84669 |
rs142724988 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423746 | GTTGGGATTACAGGC[A/G]TGAGCCACTGGGCCT | 84669 |
rs142732123 | snp | A/C | 1.64969e-05 | 0.00287196 | missense | USP32 | GRCh38.p7 | 17:60223548 | TATGTTGTCGAGCAA[A/C]GCAAACATCTGCCCC | 84669 |
rs142734238 | in-del | -/AAGTA | 0.084364 | 0.187256 | intron-variant | USP32 | GRCh38.p7 | 17:60326162 | TCACTTTGATAAAAT[-/AAGTA]AATAAGTAAGATTTA | 84669 |
rs142761382 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60376077 | AGAGACGGGGTCTCA[C/G]TCCTGTCGCCCAGGC | 84669 |
rs142766763 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP32 | GRCh38.p7 | 17:60258624 | CTCTAAGTACCTTTC[C/T]TACATTTTCTTTTCC | 84669 |
rs142787202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60292348 | AAATCCTTTACTCCT[A/C]AACAACAGATTTATA | 84669 |
rs142797231 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60206934 | CTGCTATAATATCCT[C/T]AGCATGAACAAATAT | 84669 |
rs142807683 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60297357 | TGAGCTATCTTGCCA[C/T]TGTACTGCAGACTGG | 84669 |
rs142809065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60292987 | CACCCCCACCTCAAG[A/G]CCTTTGCTATATTCT | 84669 |
rs142840528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60396328 | GTAATCCGCCTGCCT[C/T]AGTCTCCCAAAGTGC | 84669 |
rs142845447 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60263929 | AACACCATTGTGGTG[A/T]AGATCCTACCAATCT | 84669 |
rs142869159 | in-del | -/G | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60241554 | TTTCAATGTTTCTGT[-/G]GAGAGACAGGCTCTT | 84669 |
rs142882121 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60244788 | AGGCACGCACCACCA[C/T]GCCAGGCTAATTTTT | 84669 |
rs142906462 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60259601 | ATAACAAGTATGCAA[C/T]GATCATACAAATGCA | 84669 |
rs142909524 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60347377 | TTTTTTTTATGAGAC[A/G]GCATCTTGCTCTGTC | 84669 |
rs142925729 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60213177 | AATATACAAATAGCT[C/G]TGTCAGTGAGTAGCC | 84669 |
rs142939623 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B, nc-transcript-variant | CA4, USP32 | GRCh38.p7 | 17:60176781 | AAGACAATTTTTCCA[C/T]GGACTGGGGGATGGG | 84669 |
rs142945337 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403307 | AGGCATGAGCCACTG[C/T]GCCCAGCCAAGCTGT | 84669 |
rs142985645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418947 | CAACCATAGCGGAAA[A/G]TAGTGTGGTGAATCC | 84669 |
rs143028358 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406619 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 84669 |
rs143037898 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306078 | AGTACCCTTTTTTCA[C/T]TCAAAAAGAAAAAAA | 84669 |
rs143049340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60251432 | TTCCAAACAACTCTA[C/T]TTTAGTAAACTCCCA | 84669 |
rs143053128 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60340065 | ATGCTCTGTTTACTC[A/T]GACTTAAAGGTCCAA | 84669 |
rs143069047 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60204376 | GGTTGGAGTGGAGTG[C/G]TTATTTACAGGTGTG | 84669 |
rs143089485 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394177 | TCCAGGTCATTAGTT[C/T]GGTATAGAGAGACAT | 84669 |
rs143090407 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP32 | GRCh38.p7 | 17:60323823 | CCTTCATGTGAAGTA[C/T]TATATGCTTTACTGT | 84669 |
rs143109655 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60307814 | CCCCCAAGGTGTGCC[A/T]ATAAAAATCCCAAGA | 84669 |
rs143121616 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409397 | GCCACAGTATTGGCC[G/T]CTATGCACGTCGGGC | 84669 |
rs143128535 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60230397 | ACTGGCAAGAAAACA[C/G]GATAATAAAAATATT | 84669 |
rs143135626 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60319893 | TGATTTAAAGTATAC[A/G]GGGGTGAGGGGTGTG | 84669 |
rs143162869 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | USP32 | GRCh38.p7 | 17:60360302 | ACCATGGCAAAACCC[C/T]GTCTCTACTAAAAAT | 84669 |
rs143163005 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394103 | AAGACCTCAGATTAG[C/T]TGCATTACTGAAAGG | 84669 |
rs143173285 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | USP32 | GRCh38.p7 | 17:60272955 | GGGCTATGTACAAAT[A/G]CCGGGAAATTTGTTT | 84669 |
rs143213135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60222915 | TCAAACTCCTAACCT[C/T]AGGTGATCTGCCCAC | 84669 |
rs143215341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60276260 | CTCATACTAAAGAAT[A/G]CTGTTTTCGTTTTTT | 84669 |
rs143217247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60314059 | TGGAAATAGAAACTA[C/T]ATTTTAAAAAGAAAC | 84669 |
rs143226926 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60365056 | ATGCCTTTTAGTTAA[A/G]AAATCATGTTATTTC | 84669 |
rs143300048 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422113 | CTTCTCCCTTTCAGC[C/T]CTCCCTAGACCTCTG | 84669 |
rs143304435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60223960 | TTCCAAATGTTCTTG[A/G]TAGATAATGGTGATA | 84669 |
rs143348960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274419 | ATTCATGAAAACTAT[A/G]TTCCCACAGATCCAG | 84669 |
rs143383253 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60237988 | TGCTGAGGAACTGCC[A/G]AACTGTTTTCCACAG | 84669 |
rs143394829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60364171 | TCCTGACATGGTGGG[A/G]CAAAGCAAGTTCTCT | 84669 |
rs143396459 | in-del | -/AGTG | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393005 | TTTTCACAATTTCTA[-/AGTG]AGTTCAGTGGCGTTA | 84669 |
rs143409455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60366134 | AGGCATGTGACACCA[C/T]GCCGGGCTAAGTTTT | 84669 |
rs143414010 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | USP32 | GRCh38.p7 | 17:60222544 | TTCTAGTGTTAATGA[C/T]GTAGCCTGAGAAAGA | 84669 |
rs143435866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411830 | ATTTCATTCTTTCTG[C/T]GGTTGAATAATATTC | 84669 |
rs143446568 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60384394 | TCCCACTTTAGCATA[A/G]TTTTGCTTTTAATGC | 84669 |
rs143458546 | in-del | -/CTCTAG | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60328909 | ACTGGCTGTACCCCA[-/CTCTAG]CTCTAGCTCACACAC | 84669 |
rs143470557 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295571 | CCTCCCTCTTTATCC[C/T]ACCTGGGACCTGAAT | 84669 |
rs143483656 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60226643 | ATGAAGAAAATATCA[C/T]ATGTACTCAGATTCC | 84669 |
rs143489423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60243618 | TAAGGTGTCACAAAA[C/T]ATTTATCCCCTTTTG | 84669 |
rs143506662 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60281091 | TGTCTTTCCACAAAT[C/G]TGGGCAAGTTAATTT | 84669 |
rs143510962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60368761 | ATGGTTCTATACACA[A/G]CCTCGAAATGGCAAC | 84669 |
rs143531278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60350859 | GCACACTTCATCCAC[A/G]TAACGAAAAACCACC | 84669 |
rs143554831 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60298175 | TGGGACACATATAAC[A/C]GTATGCATGTGTCAG | 84669 |
rs143571114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60215027 | GACTAGAGTGCGGTG[C/T]TGTGATTTTGGCTCA | 84669 |
rs143581535 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405468 | CCTCAACCTCCCAAA[A/G]TGCTAGGATTACAGG | 84669 |
rs143590635 | snp | C/T | 0.00517822 | 0.0506191 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177229 | TGAGGAAAAACGGCA[C/T]ATGGAGGCATCCACA | 84669 |
rs143597863 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60337989 | AGGCTTTAATGCTTG[A/C]AAGAGAGTTTAGGAT | 84669 |
rs143646639 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60340935 | CACTTATGAAGCTCA[C/G]TTTGGCTAGATATGA | 84669 |
rs143648237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358235 | AATCATCACTTATAA[C/T]ATTGTTTCTACGGAA | 84669 |
rs143667322 | snp | C/T | 0.0026031 | 0.035983 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265467 | TCAGAGAGATCCATA[C/T]GTAATTCCTTTAAAA | 84669 |
rs143679318 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | USP32 | GRCh38.p7 | 17:60219103 | TTTAATCTTCAAAAA[C/T]ATGCCTTTTGCTCTG | 84669 |
rs143702944 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393508 | TTGCGTCTTCAACCT[A/G]AAAGTCACGGAATAA | 84669 |
rs143710804 | in-del | -/TC | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60301532 | ATCCTCTACCTGTCA[-/TC]TCAGAATTTTGAGAT | 84669 |
rs143754216 | snp | A/G | 0.084728 | 0.187577 | intron-variant | USP32 | GRCh38.p7 | 17:60339573 | GGGCAACAAGAGCAA[A/G]ACTCCATCTCAAAAA | 84669 |
rs143783648 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407849 | ACGCATGTAATTCCA[C/G]CACTTTGGGAGGCCA | 84669 |
rs143795688 | snp | C/G | 3.30775e-05 | 0.00406665 | synonymous-codon | USP32 | GRCh38.p7 | 17:60219722 | GGCAGGCTGCTGTCT[C/G]AGGAAGAGAAGATAG | 84669 |
rs143818870 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60217395 | TGCCTCCTGGGTTCA[A/C]GCAGTTCTCATGCCT | 84669 |
rs143830692 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60388195 | AGAGCAATATAAATG[C/T]CAGATTTTAAAGAAA | 84669 |
rs143833137 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60342378 | AGTTAGGCTACACAG[C/G]GGTCAGGAACCCACT | 84669 |
rs143848756 | snp | C/T | 0.000148252 | 0.00860837 | missense | USP32 | GRCh38.p7 | 17:60198353 | TATAGGTCTTTCTTC[C/T]GGGTATGCACAGTAC | 84669 |
rs143882926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60293697 | GGCAGTCCAAAGATA[C/T]ATCAGAACCAGATAC | 84669 |
rs143894362 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411076 | GCTCACACCTGTAAT[C/T]TCAGCACTTTGGGAG | 84669 |
rs143900080 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60207712 | GAATTCTAGTAACAG[C/T]GGTAATACAGAAGAG | 84669 |
rs143958745 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60315096 | CACACCTACAAGAAC[A/G]GCTATAATAAAATGA | 84669 |
rs143969798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60277449 | CCTTGCATCACTAAC[A/G]GATAAGAGGATAATG | 84669 |
rs143971219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423475 | TGGGATTACAGGTGT[C/G]AGCCACTGTGCCCAG | 84669 |
rs143998206 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266295 | ATCATGAATCTGTAT[C/T]TCTAAATCATTATTC | 84669 |
rs143998563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318473 | ACTTGTTCACATCTC[C/T]AGAAGGGAAAGTTCC | 84669 |
rs144055742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60191899 | TCCCTGTTGTAACAG[C/T]AATGACCAATCAATC | 84669 |
rs144072484 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP32 | GRCh38.p7 | 17:60315825 | TAAGTAAATAAGTCT[C/T]TATAGCATGGCCTGT | 84669 |
rs144077758 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60386038 | ACACACACACACACA[A/C]CACAAAAGAAACAAA | 84669 |
rs144090363 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60271242 | CCATTAAACCTGCAA[A/G]CATATGAGAAGATGG | 84669 |
rs144119370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320558 | AGGGAAGAAACCGGG[A/G]TACCTGGAGAAAACC | 84669 |
rs144122809 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60391649 | ACGGGCACTGCCCTG[C/T]CAGCGCCGATCCCCC | 84669 |
rs144136223 | snp | A/G | 4.94344e-05 | 0.00497139 | missense | USP32 | GRCh38.p7 | 17:60226174 | GGGCTGCAGTTCCAA[A/G]TGAGTATTTTCCTCC | 84669 |
rs144158255 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60239826 | ACAACCTCCGCCTCC[C/T]GGGTTCAAGGGATTC | 84669 |
rs144170255 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60355337 | GATAGAAATGTTCTG[A/T]ATCTTGTCAAAATGC | 84669 |
rs144186406 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420103 | ATTTTATTTGTTTTG[C/T]TTTATTTTATTTATT | 84669 |
rs144192242 | snp | A/G | 0.000181241 | 0.00951777 | synonymous-codon | USP32 | GRCh38.p7 | 17:60236138 | AGGAATCTAACTCAC[A/G]TATTTGACATATTCT | 84669 |
rs144233314 | snp | A/C/G | 1.64942e-05 | 0.00287173 | missense | USP32 | GRCh38.p7 | 17:60209522 | ACCCATTAAACCTGG[A/C/G]AGCATATTTTGCTAT | 84669 |
rs144234740 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60361707 | GTATAGCCTATCTAA[A/G]GGTAGCTGTTTAAAT | 84669 |
rs144246666 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306678 | TATTAAAAAAGGAAA[A/G]GCCAGAGCAATCAGG | 84669 |
rs144285646 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60311247 | GATCACATGTACCCC[C/T]CAAAAAATGTATCTA | 84669 |
rs144295301 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60246804 | GATGTTGAGCATTTT[C/T]TCATATATCTGCTGG | 84669 |
rs144299601 | snp | C/T | 0.0210169 | 0.100333 | intron-variant | USP32 | GRCh38.p7 | 17:60180514 | TTGATATTCTGTTTC[C/T]AACTTTCATTCAAAG | 84669 |
rs144315222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60229384 | TGTGATCTCACTACA[C/T]ATGCAGCCAGAATTA | 84669 |
rs144335865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418956 | CGGAAAGTAGTGTGG[C/T]GAATCCTCAAAGAGC | 84669 |
rs144338483 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60186267 | CCTATAAGGGATTAC[A/G]TGTGAGCTGGCCCTC | 84669 |
rs144349438 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60294471 | TAAGTATGAATAGTT[A/G]CCTTTACAGTAGAAT | 84669 |
rs144355273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306225 | AGACGGAGTGTGAAT[A/G]GGATAGCAAGGATGC | 84669 |
rs144361832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415754 | TTTTCTTGGAGTCTT[C/T]ATACAATTCTAATTG | 84669 |
rs144376024 | snp | A/G | 0.077417 | 0.180873 | intron-variant | USP32 | GRCh38.p7 | 17:60234782 | GAGTCTCACTATGTT[A/G]CCCAGGCTGGTCTTG | 84669 |
rs144429400 | snp | A/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60361734 | AAATAATGAAGAAAA[A/T]TCAATATCCACTTAT | 84669 |
rs144442494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298888 | AGCACTTTGGAAGAC[A/T]GAGGCAGAAGGATCA | 84669 |
rs144453913 | snp | A/G | 9.89087e-05 | 0.00703168 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183223 | TTTGCTCAGGAGCAC[A/G]TCCTCTTCCCCAGCC | 84669 |
rs144457236 | snp | A/C | 4.94197e-05 | 0.00497066 | missense | USP32 | GRCh38.p7 | 17:60181433 | TTGCTGTAGCCATTG[A/C]CACATGCTTCATGCT | 84669 |
rs144482967 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60248039 | ATTTGTCTGTTCTTA[C/T]GTCAGTGCCATGCTG | 84669 |
rs144540150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416586 | ATGGAATTTTGAAGA[A/G]TGCTCCCAAAGGCAA | 84669 |
rs144544967 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178577 | GCTCTGGGTGGAAGG[C/T]ACACAGCTCTTAAGA | 84669 |
rs144565273 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60337837 | AATGAGCCATGATCG[A/G]GCCACTGCACTCCAG | 84669 |
rs144582327 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402917 | CAGCCCACTGTGCTT[C/T]CTCTTTCCTGACAAC | 84669 |
rs144593211 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404815 | TAAATAGAAGGCTGG[C/T]CTTTTTACTTAACAG | 84669 |
rs144618313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60285739 | AAGAAGGCAAGAAAA[G/T]GTTTCATGAAAAAGA | 84669 |
rs144626921 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60374840 | CTTATGGGATCACAG[C/T]TGTGTATGCAGTCCA | 84669 |
rs144627198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407958 | TAAAAATCAGCTGGG[C/T]GTGGGGGTGAGCGCC | 84669 |
rs144629589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60285909 | TGAGAGGCCAAGGCA[C/G]GTGGATCACCTGAGG | 84669 |
rs144658472 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60283286 | AGGCAAAGAACACAC[A/G]TGAGGAGAAATGAGC | 84669 |
rs144688578 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | USP32 | GRCh38.p7 | 17:60290823 | GGGCTTAAAGTTGAG[C/T]TGATTACCAATGGTC | 84669 |
rs144693498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254177 | CAAGTTAAATATTTG[C/T]GAATAACTATAAAAA | 84669 |
rs144696163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231392 | CTCTAGAGTGCTAGA[C/T]AAAGTAATAAAATAA | 84669 |
rs144699678 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | USP32 | GRCh38.p7 | 17:60341864 | ATACTCCTTTAGCTC[G/T]GAGAAGTTTGTTATT | 84669 |
rs144700003 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60287390 | CCATGTATTGATTTA[C/T]GATTTTTGCCTGTAG | 84669 |
rs144710628 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60209731 | CAAATGACCCCCCCC[-/C]AAAAAAAGAGAAGTA | 84669 |
rs144739585 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60206310 | TGACAGAGTGAGACC[A/G]TTTCTCAAAATAAAT | 84669 |
rs144748838 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | USP32 | GRCh38.p7 | 17:60218747 | TAGCTGAAATTACAG[C/T]ACCACCACGCCCAGC | 84669 |
rs144751700 | snp | A/C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395562 | GTCTGAAGTCTGCTT[A/C/G]TCATGCTGAAAGGAA | 84669 |
rs144763887 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP32 | GRCh38.p7 | 17:60276380 | CAAAGGAATCTGATA[C/T]ATAAATTGAGATTCC | 84669 |
rs144782086 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60310003 | GAGCCGAGATTGTGC[A/C]ACTGCACTCCAGCCT | 84669 |
rs144788971 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60216481 | TCATGAGTTAGCTTC[C/T]TTCTTCCTGAAAAAT | 84669 |
rs144802777 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60259348 | GCCCTTTTTGTTTGT[A/G]TTGTAAACAATTCAC | 84669 |
rs144851274 | in-del | -/TT | 0.00796324 | 0.0625956 | intron-variant | USP32 | GRCh38.p7 | 17:60246712 | CAGAATCAGTTATTC[-/TT]TGTCTTTTTTATAAT | 84669 |
rs144887558 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416086 | CTCATGATCTGCCCG[C/T]GTCGGCCTCCCAAAG | 84669 |
rs144928841 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60398765 | AGAGGATTGATTGAG[A/G]TCAGGAGTTCAAGAA | 84669 |
rs144929681 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60301166 | TCTGTACAAGTTTTT[G/T]TGTGTGTGTGTGGTA | 84669 |
rs144967178 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60381684 | GTACCCTTGCAAATG[C/T]TGCTTTCTAGATCTT | 84669 |
rs144993584 | in-del | -/TA | 0.355941 | 0.226443 | intron-variant | USP32 | GRCh38.p7 | 17:60323274 | AAATAAACAAAATGT[-/TA]TATATATATGCATAC | 84669 |
rs144994340 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231176 | ATAGTTTATGTGTTC[A/T]AAAATATGGGTCAAG | 84669 |
rs144997344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60357216 | AGAACTCTGAGTGGT[C/T]CAGGTGGGAGGACAG | 84669 |
rs145006662 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421991 | TCTTTATACACCCCC[A/G]AAACACACACATCCC | 84669 |
rs145015306 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60193426 | AGCTACATACCATTT[C/T]TGGAGTAACTGCTTT | 84669 |
rs145024243 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60387233 | ATACTGAGAAATTGG[C/T]GAACAAAATCTTAGT | 84669 |
rs145024776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60351953 | CTGGCAAAAAAAAAC[A/G]CAAAGGGCTATTCTA | 84669 |
rs145026879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60264180 | TTACATGCTTATTCT[A/G]GCTACCACTAAAGGA | 84669 |
rs145047657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60268768 | ATTAAATCAATTGAG[C/T]GCATCATAGTACAAC | 84669 |
rs145057528 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60357383 | GCTTGAGCCCAGGAG[G/T]TGGAGGCTGCAGTGA | 84669 |
rs145060407 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60307246 | CTGGGATTACAGGCA[C/T]GCACCACAATACCCA | 84669 |
rs145067535 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60260409 | GTGCCTGTAATCCCA[A/G]CTACTCAGGAGGCTG | 84669 |
rs145100882 | snp | C/T | 0.0050163 | 0.0498296 | missense | USP32 | GRCh38.p7 | 17:60214624 | ATGCCTCTTACCTCA[C/T]TGTTGTATAGCCACA | 84669 |
rs145115039 | snp | A/G | 0.102726 | 0.202016 | intron-variant | USP32 | GRCh38.p7 | 17:60203719 | GTAGCTAGGACTACC[A/G]GCGTGTGCCACCATG | 84669 |
rs145121439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354129 | TATTATTACTCATTA[A/C]ATGGTATAAAATATT | 84669 |
rs145135502 | snp | A/G | 0.00019784 | 0.00994389 | synonymous-codon | USP32 | GRCh38.p7 | 17:60192855 | TTACCTATACCATGG[A/G]CACCAAGCACAGGAG | 84669 |
rs145187351 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60363778 | TGCTGAGATTATACA[C/T]GTGAGCCACTGTGCC | 84669 |
rs145187514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235195 | TTAAAACATTAACAA[C/T]CACTCATTCTAAGGC | 84669 |
rs145209160 | in-del | -/TA | | | intron-variant | USP32 | GRCh38.p7 | 17:60361865 | AGAGAAAGATACATG[-/TA]TATATATATATGCCA | 84669 |
rs145255314 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60372660 | GTCTGGGTAACACAG[A/T]AAGACCCCGTTCTCT | 84669 |
rs145292019 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP32 | GRCh38.p7 | 17:60239688 | TTCTCTTTATTGATA[C/T]TCTATTTGTACATAT | 84669 |
rs145365507 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60336246 | AACTCTGTTTTTCAA[C/T]AGCTTATGAAGCTGT | 84669 |
rs145391697 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60327344 | GAGCAGCAATAGTGG[C/T]AGTGGGTCCCCTGTG | 84669 |
rs145393574 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407629 | CAACAATGTGACATC[C/T]ACATTAGCCAGGTGT | 84669 |
rs145395429 | snp | G/T | 0.000463062 | 0.0152091 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269504 | ATAACCCACAGGATA[G/T]CTCCTTAAAATCTAT | 84669 |
rs145397314 | in-del | -/TTGT | 0.131381 | 0.220067 | intron-variant | USP32 | GRCh38.p7 | 17:60375602 | TCTGGTGTTTTGTTG[-/TTGT]TTGTTTGTTTGTTTT | 84669 |
rs145410669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288481 | AGCCAATTATATATA[C/T]AAAAAAAGGCAAACA | 84669 |
rs145421736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60188240 | CTGAGGTCCCAACAG[G/T]AGAGAAATGTAAAGG | 84669 |
rs145423121 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393992 | CCCCACCAATATTTC[G/T]TGTTTTTCTACTCAC | 84669 |
rs145448131 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60195389 | GTCGCCCAGGCTGGA[A/G]TACAGTGGTGTGATC | 84669 |
rs145448231 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60240939 | GAGTTAAGTATAACA[C/T]AGCTGAGCATCTTGC | 84669 |
rs145476706 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60221496 | ACATTATAAAAGGAA[A/G]AGTGTTTCTTTCTTT | 84669 |
rs145488890 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60343269 | GTTAACAAGGATATC[C/T]GGGACTTGAACTTAG | 84669 |
rs145497360 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411265 | GGAGGTGGAGGTTGC[A/G]GTGAGCCGAGATTGC | 84669 |
rs145517427 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294994 | ATCTTTTCAAACATG[A/C]CAAATTTGCAAAAAT | 84669 |
rs145524585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210416 | TCCCAGGTTCAAGCG[C/T]TTCTCGTGCCTCAGC | 84669 |
rs145562207 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60278786 | AGATGACTTGGAGCT[C/G]CTAGACTGCTTGGAG | 84669 |
rs145592518 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60350214 | GCGATGGGGTTTTGC[C/T]ATGTTGCCCAGACTG | 84669 |
rs145625464 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422799 | TTTCATTCATTCAGA[A/T]GTTTATGCATGACCT | 84669 |
rs145653296 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60308181 | ATCAAGGCAAGAATC[C/T]GGGATACAGAAAACC | 84669 |
rs145667783 | snp | C/T | 0.000153988 | 0.00877328 | missense | USP32 | GRCh38.p7 | 17:60190619 | GATCCCAATCCACAG[C/T]GATATAGGCATTTCC | 84669 |
rs145690333 | snp | C/T | 3.29674e-05 | 0.00405988 | missense | USP32 | GRCh38.p7 | 17:60185575 | TCACTGGTGAAAGCA[C/T]GGAGACAGCTGTCCA | 84669 |
rs145715720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60387314 | AAAGTACTGAATTAT[C/T]AACTGTTACATGCTT | 84669 |
rs145720299 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60301469 | GTTGCACATTTTTTA[G/T]GTGTTTATTTACCAC | 84669 |
rs145734929 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60214989 | TGTTTGTTTTTAATA[C/G]ATGGAGTCTTGTTAT | 84669 |
rs145764781 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP32 | GRCh38.p7 | 17:60326527 | TGGTCTTGAACTCCT[A/G]ACCTTGGGTGATCCA | 84669 |
rs145795828 | snp | C/T | 0.000307953 | 0.0124049 | missense | USP32 | GRCh38.p7 | 17:60214642 | TTGTATAGCCACAGG[C/T]GCATATCTTCCTCTT | 84669 |
rs145797978 | snp | A/T | 1.64868e-05 | 0.00287109 | stop-gained | USP32 | GRCh38.p7 | 17:60223478 | TGAGGGTTAAGGTGC[A/T]ACAAAATATTCCCAT | 84669 |
rs145799359 | in-del | -/A | 0.0205511 | 0.0992634 | intron-variant | USP32 | GRCh38.p7 | 17:60356421 | TGACCTTAAACCTCC[-/A]CACAAGCAGGAAGTG | 84669 |
rs145836234 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60242602 | TTTTAGTAGAGATAG[C/G]GTTTCGCCATGTTGG | 84669 |
rs145866578 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60242376 | AAAAACAATAAAAAT[G/T]ATAATAAAAATAACC | 84669 |
rs145894628 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306711 | AGAGAAAGAAATAAA[-/G]GGTCTCCAAATTGGA | 84669 |
rs145921314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409094 | GGCTCATGCCTGTAA[A/T]CCCAGCACTTTGGGA | 84669 |
rs145926251 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | USP32 | GRCh38.p7 | 17:60341136 | CCTTAGTGAATCTGA[A/C]AACTATGTGTCTTGG | 84669 |
rs145928074 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60281501 | TGAGATCATGCCACT[A/G]CACTCCAGCCTGGGC | 84669 |
rs145933280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60370247 | ACACATCTTTAAGAA[A/C]TAAAATGATGACAAC | 84669 |
rs145944956 | in-del | -/ACC | 0.00398564 | 0.0444627 | cds-indel, intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178153 | AGTTGACTTCCTAAA[-/ACC]ACCAATTTCATTAAA | 84669 |
rs145954033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60229920 | CTGGGTTCAAGCAAT[C/T]CTCCTGCCTCAGCCT | 84669 |
rs145974061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233188 | CTGTTTTAAAATACT[G/T]AACAAGAGTCTGGGT | 84669 |
rs146017030 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60394904 | GCACACCATCCCGCC[C/T]GGCTAATTTTTGTAT | 84669 |
rs146032517 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412157 | CAAGCTCACCACACC[A/G]GTATTTTCCAAATTT | 84669 |
rs146035106 | snp | A/G | 0.132751 | 0.2208 | intron-variant | USP32 | GRCh38.p7 | 17:60401302 | GTGAACCAGGGAGGC[A/G]GAGCTTGCAGTGAGC | 84669 |
rs146035705 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP32 | GRCh38.p7 | 17:60366014 | CGGAGTTTCGCTCTT[A/G]TTGCCCAGGCTGGAG | 84669 |
rs146038055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60277748 | ACCATTCAAAGAAAT[C/T]ACTCAGTTAGCAAGC | 84669 |
rs146048628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60258689 | TGCAAGAGAACACTT[C/T]GCTGTTTTACAGTCA | 84669 |
rs146054672 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60346236 | AAGCATGAGCCAGCA[C/T]GCCAAGCCAAAATTC | 84669 |
rs146072369 | snp | A/G | 0.000181227 | 0.00951738 | synonymous-codon | USP32 | GRCh38.p7 | 17:60236144 | CTAACTCACGTATTT[A/G]ACATATTCTTTCCAC | 84669 |
rs146076142 | snp | C/T | 0.135143 | 0.222054 | intron-variant | USP32 | GRCh38.p7 | 17:60212771 | TTCCTTTTTTTTTTT[C/T]TGAGACAGTCTGGCT | 84669 |
rs146139758 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378897 | GTACATTTTTTAAAA[G/T]AGTTCAAATGGTAAA | 84669 |
rs146159338 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60342052 | GGTTTTTATCTATCT[C/T]TGGTCTTTGATGTTG | 84669 |
rs146159562 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60254602 | TACTTGGGAGGCTGC[A/G]GAAGGAGAATGACCT | 84669 |
rs146170956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60233757 | CTTATTAATAAGTTG[C/T]CATAGTTCCCTGTCT | 84669 |
rs146179201 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60349214 | AGACTACCTGTATAA[C/T]AGTATAGGTAATCTC | 84669 |
rs146180377 | snp | C/T | 0.100588 | 0.200439 | intron-variant | USP32 | GRCh38.p7 | 17:60324528 | GTTATTAATGGTAAT[C/T]AACAACATGTAAATG | 84669 |
rs146208027 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60197238 | TCAAAATACCCCATA[A/T]CATAACAAATAAGTA | 84669 |
rs146260446 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | USP32 | GRCh38.p7 | 17:60370617 | AAAAATACAAAAAAA[A/T]TTAGCTGGGCATGGT | 84669 |
rs146274347 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60320172 | ACTGCAACTTCAAAT[A/G]ACACCAGGTAGAATG | 84669 |
rs146279461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60230734 | TTCTTCCCCTTCCTA[C/T]ACGCTTATTTTTCTT | 84669 |
rs146298957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60304434 | AAGAAAGTACCTCAG[A/G]CTGGAGGAAATATTA | 84669 |
rs146326619 | snp | A/G | 0.000691711 | 0.0185843 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183340 | CTGGCAGAGAGCCGG[A/G]TCTCTTGGTACCAAA | 84669 |
rs146328593 | in-del | -/CAGAAGCAGTGGGT | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422520 | GAGACGGCTAGGTCA[-/CAGAAGCAGTGGGT]CAGAAGCCAGAGGGG | 84669 |
rs146337114 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60258300 | TTAAGAGAAAAACTG[C/T]TGTCAGTTTGAGGAT | 84669 |
rs146379809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414937 | CTAGCTGCAACCTAC[A/G]GTCTCCCGGGTTCAA | 84669 |
rs146382867 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | USP32 | GRCh38.p7 | 17:60346895 | ACTACAGCAAAGCAC[A/G]GAGTAGCAAACGATA | 84669 |
rs146394103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298412 | TTATAGATATCATAA[C/T]TTTTTTCAGTTGACA | 84669 |
rs146398372 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60212959 | GATTTCACCATGTTG[G/T]CCAGGCTGGTCTGGA | 84669 |
rs146400293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60353152 | TTATAAGGATAGGAC[A/G]CTGAACTTACAGGAT | 84669 |
rs146462923 | snp | A/C/T | 0.00637159 | 0.0561118 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407872 | GGAGGCCAAGGCAGG[A/C/T]GGATTGCCTGAGGTC | 84669 |
rs146483883 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | USP32 | GRCh38.p7 | 17:60391787 | GCCTCAGGCGCCCCA[A/C]GCCCTCAATCTCCCC | 84669 |
rs146485373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60268268 | TTTAAGACAACAATT[A/G]ACTTTAATGGAAATG | 84669 |
rs146485471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320587 | CCCACACAGACATGT[A/G]GGGGAGCATGCAAAC | 84669 |
rs146497122 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60274244 | CTTGAAGGACAGGCA[A/G]TAGAAACTATCTAAA | 84669 |
rs146534448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60207235 | TTAGGCGCTTTCATC[C/T]GTAAAACCAACGAGA | 84669 |
rs146544566 | in-del | -/AC | | | intron-variant | USP32 | GRCh38.p7 | 17:60386019 | TTCTATTGCTGCATA[-/AC]ACACACACACACACA | 84669 |
rs146577219 | snp | C/T | 0.0742686 | 0.177816 | missense | USP32 | GRCh38.p7 | 17:60211060 | TTCCACTCCAAAGTT[C/T]CTGCACTAAATCACC | 84669 |
rs146580750 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | USP32 | GRCh38.p7 | 17:60190629 | CACAGCGATATAGGC[A/G]TTTCCAATGAAAGCT | 84669 |
rs146586655 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | USP32 | GRCh38.p7 | 17:60386949 | CTACTTAAAAACTGC[C/T]CCATTTTTCTCCTTT | 84669 |
rs146600389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60335791 | GGCAATGGGTCATGT[A/G]CTTTTGTTGAAGGTT | 84669 |
rs146605863 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60243002 | TAAGTTTTCAAATCC[A/G]TTTACGTACATTTTC | 84669 |
rs146616953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60248892 | CATGTCTCATAATTT[C/T]TTCTTGTTGAAAACT | 84669 |
rs146626088 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60339305 | AAGGTATAAATGGCC[A/G]AGCATGGTGGCTTAC | 84669 |
rs146652488 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | USP32 | GRCh38.p7 | 17:60192603 | CCACGCCCCGCTAAT[C/T]TTTGTATGTTTAGTA | 84669 |
rs146667931 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408185 | AGAAGCAGGGGGGAA[A/T]AATCAGGTGACAGAC | 84669 |
rs146719060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312303 | TTTTTCCAGAGTAAA[C/T]TCTAGTACACCAATC | 84669 |
rs146721341 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60222673 | ATGTTGCTGGAAAAA[-/C]TTAATTTTTTTTTTT | 84669 |
rs146723044 | snp | A/G | 0.000399281 | 0.0141238 | missense | USP32 | GRCh38.p7 | 17:60222452 | TACCAGTGATAAAGT[A/G]CTCTCCACACAGGTT | 84669 |
rs146725059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60366138 | ATGTGACACCACGCC[A/G]GGCTAAGTTTTTTTT | 84669 |
rs146736089 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | USP32 | GRCh38.p7 | 17:60226671 | TCCATCATTTAGCAA[C/T]AACTGTGTTTTAGTT | 84669 |
rs146805752 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60422433 | AAATGGGAGCGGGGT[C/G]GGGGGCTGGGTTCTG | 84669 |
rs146822514 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60311834 | CACCTCAAACAAAAC[-/A]AAAAAAAAACGGTAG | 84669 |
rs146827049 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60362665 | AATGACTATTTAACA[C/T]ATGTTGATGACAAAT | 84669 |
rs146831188 | in-del | -/GGGGGGGGGG | | | intron-variant | USP32 | GRCh38.p7 | 17:60354913 | GCTGGGCATAGTGGC[-/GGGGGGGGGG]GGTGCCTGTAGTCCC | 84669 |
rs146844693 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410653 | AGCCTGGGCCACAGA[C/G]TGAAACACTGTCTCA | 84669 |
rs146844808 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | USP32 | GRCh38.p7 | 17:60203766 | ATTTTTAATAGAGAC[A/G]GGGTTTCACCATCTT | 84669 |
rs146847510 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394051 | GGCATTAGTCACAGC[A/G]CTGCCCTTTCCAGTT | 84669 |
rs146847602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289350 | ATCCAATTTTTCACT[G/T]GCCTTATCCCTCTTC | 84669 |
rs146847764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60342504 | AGAAGTTGTCTGCTG[C/T]ATTTTGTTCAGCTAT | 84669 |
rs146857227 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60209870 | GCTCACATTGAAAGA[C/T]ATCCTGTTCTATAAC | 84669 |
rs146867233 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60294024 | TTGTTTAATTTTTCT[A/G]TAAAGACACAATGAA | 84669 |
rs146901167 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60201656 | ATTACTAGTGTCGTT[A/G]ATCATTTTTTTTTTT | 84669 |
rs146907845 | snp | A/G | 0.000445953 | 0.0149257 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271449 | TCAATAACCAATAGC[A/G]TTTCTCAAGATCAAT | 84669 |
rs146907902 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60275453 | CAGAGCAAGACTCCA[A/T]CTCAAAAACAAACAA | 84669 |
rs146908333 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | USP32 | GRCh38.p7 | 17:60329651 | CCTTATTACTTTTCT[A/C]CCTTCCTCAACTCTT | 84669 |
rs146922159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60343838 | GGAGTTCAAGACCAG[C/T]CTGGCCAACATGGTG | 84669 |
rs146924167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256931 | ACTGACCAACAACGT[A/G]ATTTCATCATTCTAA | 84669 |
rs146994610 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378532 | CACAATAGCCAAAAG[A/G]TGGAAACAACTCAAA | 84669 |
rs147029535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60191800 | ACGCGTGAGCCACCA[C/T]GCCTGGCCAATGCCT | 84669 |
rs147029549 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231965 | TCTAAGAAAGGATGG[C/T]TCATTTTTCCTGATC | 84669 |
rs147067023 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414115 | CGCCTATAATCCCAG[A/C]GCTTTGGGAGGCCAT | 84669 |
rs147083637 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60365085 | TCAAAAAGGGAAAGT[G/T]TTTTTTAAATGAAGA | 84669 |
rs147110730 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60229115 | GGGTCTTGCTCAGTC[A/G]CCTATAGCTCACTAT | 84669 |
rs147139044 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60384520 | CCCTAGGCCAGGCAC[A/G]GTGGCTCATGCTTGT | 84669 |
rs147155483 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60354752 | CAAATGAATCCAAAA[A/G]AGTATGATATAAGGC | 84669 |
rs147166981 | snp | C/T | 6.83913e-05 | 0.0058473 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183169 | CCAGGCCTCACCTTT[C/T]GGGCTGCTGATGATG | 84669 |
rs147171919 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60360637 | CTGAGATTGCACCAC[C/T]GCACTCCAGCCTGGG | 84669 |
rs147189913 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60286685 | TAGTAGCCTAAAAGA[A/T]GATGTTTGATTTCCC | 84669 |
rs147204628 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60205862 | TTTGGCCAAATGAAA[A/G]GGAAAGAGTAACTGC | 84669 |
rs147230634 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60278983 | AAAGAGTATTATAAG[-/A]AAAAAACAAAAATGA | 84669 |
rs147273206 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60338176 | AAAAAATACAAAAAA[A/T]TAGCTGGGCATGGTG | 84669 |
rs147275848 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405906 | ACTCCTGTAATCCAG[C/T]ACTTTGGGAGGCCAG | 84669 |
rs147296064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60318603 | GTGACAAAATCATTA[A/G]TGGCTTTTAGCTGCA | 84669 |
rs147296142 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60266326 | AGATATAAGACCCTA[A/C]CCTTCAGCCAAATCT | 84669 |
rs147305887 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60272034 | TGGTCAGGCTGGTCC[C/T]AAACTCCTGGTCTCA | 84669 |
rs147310540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60192008 | CAAACTTATATTTAA[C/T]GAGAGGCTTGGCGTG | 84669 |
rs147349022 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60376123 | CAATCATGGCTCACT[A/G]CAGCCTCAAATTTCT | 84669 |
rs147350613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423841 | CATCCACTTTTTCTG[A/C]ATAGTCATTAGATGC | 84669 |
rs147383770 | snp | C/T | 8.25103e-05 | 0.00642249 | missense | USP32 | GRCh38.p7 | 17:60226039 | ATAGGTCATATTTAC[C/T]GCTGCCAGCAGTTTC | 84669 |
rs147394191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60240104 | ACATATTTAAGATAA[C/T]TGATTTTAAATGTTT | 84669 |
rs147413172 | snp | A/G/T | 0.274099 | 0.248843 | synonymous-codon, missense | USP32 | GRCh38.p7 | 17:60208181 | GTCTTAGTCCATACC[A/G/T]TACAGGGGTAGTACC | 84669 |
rs147417977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60245222 | TTTCTACTATTGGTG[C/T]TCTTTATTTTTTTTT | 84669 |
rs147427178 | in-del | -/ATAG | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232824 | CAAAGTGCTGGGATA[-/ATAG]ATAGGCGTGAGCCAC | 84669 |
rs147456113 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407088 | AAATTCTGTGATTTT[C/T]CTAGCTTTTTGCCTA | 84669 |
rs147471684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409504 | GAGGGAAAAAAAGAG[A/G]GTTACCTAATGCATT | 84669 |
rs147489517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60292437 | TTACAACTTTCTTGA[C/T]ATCCAACCCCCTAAC | 84669 |
rs147498263 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60220800 | AGGAGCCCGCCACCA[C/G/T]GCCTGGCTAATTTTG | 84669 |
rs147518129 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60315072 | CAAAACCACAATGAC[A/G]TACCACTTCACACCT | 84669 |
rs147522072 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60185397 | ACAAAACCTCCTGTT[C/T]GTTCATGTCTTCTTT | 84669 |
rs147522112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60224398 | GAAAGGGAGGGAAGA[A/G]GCAGATTCTACAAGG | 84669 |
rs147531613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60189350 | TTCCCCAGTCCTCCA[C/T]AGCACAACAAGACAG | 84669 |
rs147560846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60260548 | ATACAGGAATAAATC[A/G]TAGCATAATCATAAT | 84669 |
rs147561473 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60348605 | CATAGTGAGACCCTG[C/T]CTCTACAAAAACAGA | 84669 |
rs147594374 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60217355 | GAATAGAGTGCATGG[C/T]GCGATCTCGGCTCAC | 84669 |
rs147650181 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60380870 | TAGAAATTTGTGCTT[A/G]TCCTTGCATATAAGG | 84669 |
rs147661323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60328178 | CCAGGCACAGCAATC[C/T]ATAGACCAATCAGTG | 84669 |
rs147675052 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60195485 | TGGGATTACAGGCAC[A/G]TACCACCATGCCCGG | 84669 |
rs147694276 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60282847 | GTACACTTTAAGAGG[C/T]TGAAAAATTTTCAAT | 84669 |
rs147698068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60199863 | TTTCTCAGTTACTAC[A/T]GAGATAAATTCTACT | 84669 |
rs147703757 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60201734 | CATGATCTCGGCCCA[C/T]TGCAACCTCTGCCTC | 84669 |
rs147738818 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60373595 | GCTAGGATTACAGGC[A/G]TGCACCACCACAACC | 84669 |
rs147769627 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60379249 | ATGCAAATGTCAAAG[C/T]AGCACTGGCATAAAT | 84669 |
rs147771097 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306784 | TTATATTTAGAAAAA[C/T]CTAAAGATTCCACCA | 84669 |
rs147778127 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60180769 | ATATTTTAGAACCCT[C/G]TAACTTTTTCTAAAA | 84669 |
rs147781268 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60255801 | TCTGAATTTTATCAA[C/T]GCAGTAAGAAATACT | 84669 |
rs147802630 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60186960 | TCACACAGTATATAT[C/T]TGTGTCCCAAAGCAG | 84669 |
rs147804103 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60259721 | TCCTTATAATTTTCA[C/T]TTTGCAAATTTATCC | 84669 |
rs147849426 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | USP32 | GRCh38.p7 | 17:60183237 | CGTCCTCTTCCCCAG[C/T]CGAACTCTGCGCATC | 84669 |
rs147853035 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60301917 | ACTGTAAAATACGTA[C/G]AGATGGTCCTCAGCT | 84669 |
rs147857748 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420317 | TTGTTTTAAAACTTA[G/T]CATTATATAATGTTT | 84669 |
rs147886293 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60287842 | TCTCAGGCCGGGCAT[C/G]GTGGCTCACGCCTAT | 84669 |
rs147909831 | snp | A/C | 0.0770498 | 0.180522 | intron-variant | USP32 | GRCh38.p7 | 17:60234783 | AGTCTCACTATGTTG[A/C]CCAGGCTGGTCTTGA | 84669 |
rs147948547 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60399210 | AGGCGCTGAAGATAC[A/G]GAATTGAGCAAAGTA | 84669 |
rs147965535 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | USP32 | GRCh38.p7 | 17:60367049 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT | 84669 |
rs147965557 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403081 | CAGTGTCACGATCTC[A/G]GCTCACTGCAACCTC | 84669 |
rs147998157 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60243676 | AAAACATTTTTAGCT[C/T]GCAGATTGTACAGAA | 84669 |
rs148010211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229619 | TTTTGAAAGAGTAAC[A/G]GCGCCACCTTTGAGA | 84669 |
rs148018980 | snp | C/T | 1.65252e-05 | 0.00287443 | synonymous-codon | USP32 | GRCh38.p7 | 17:60301669 | ATTATTGAAGTGCAG[C/T]CCTTTGGATGTTCCA | 84669 |
rs148019639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60318906 | AATGGGATATTATTC[A/G]GTCATAAAAAGGAAT | 84669 |
rs148029152 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60302711 | GTGCAATTACACAAC[G/T]TCCTTCAAACCTGGG | 84669 |
rs148033940 | snp | C/G | 0.077417 | 0.180873 | intron-variant | USP32 | GRCh38.p7 | 17:60215043 | TGTGATTTTGGCTCA[C/G]TGCAGCCTCCACCTC | 84669 |
rs148034797 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405620 | ACAAAAATTAGCCAG[A/G]CCTAGTGGCATGTTG | 84669 |
rs148043947 | snp | A/G | 0.0543475 | 0.155628 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177926 | AAAGACCAAAAATAA[A/G]GTGAAACATTTCCTT | 84669 |
rs148080804 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60219288 | GACCAGTCAATGACT[A/G]GTATACTACTACTTA | 84669 |
rs148122062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60351433 | AAATGTCTACTATGC[C/T]AGGCTTCTTTTTTTT | 84669 |
rs148158108 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60388740 | TCCCTAACAGTGTTT[A/C]AATGTACACTTTTAG | 84669 |
rs148174666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60358784 | ATGACGGTGCTTCGC[A/G]AGGTTTTGATATTAC | 84669 |
rs148177339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60270325 | AAGTACTCTAGAAAT[C/T]TGAAGAATACAGATA | 84669 |
rs148177663 | snp | C/T | 0.000181191 | 0.00951644 | synonymous-codon | USP32 | GRCh38.p7 | 17:60222490 | CATTTCATAGTCTCT[C/T]CCATGAATCAGCTGT | 84669 |
rs148203054 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60204533 | GAGTGCTGTGGCGCA[A/T]TCTTCGCTCACTGCA | 84669 |
rs148207782 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60323860 | AAAAGCGTCAAAACA[C/T]CTCTACAGCTTCTGC | 84669 |
rs148210645 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60394239 | CAGAGTGCGAGTTCC[C/G]AGTTAGATTATCGTA | 84669 |
rs148230590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60276394 | ATATAAATTGAGATT[C/T]CTAAATAAGATGTCT | 84669 |
rs148240080 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60258053 | AAAAAGGGAGCAAGC[A/C]GATAAGATGAAGAAG | 84669 |
rs148243877 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60345240 | TGTTCCTATGATCAT[A/T]ATCAGTGGCTATTAA | 84669 |
rs148293377 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60264209 | GACACAGGAGAGGTC[C/G]TTACCACAACCATTT | 84669 |
rs148340395 | in-del | -/ATTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60236513 | TTAATTAATTAATTA[-/ATTA]CATTTTTTGCAGAAT | 84669 |
rs148387519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60314676 | GTGAACAGAAACATA[C/T]TTGAAGAACAGTACT | 84669 |
rs148387557 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414573 | AGCAGAGATTACAGG[C/T]GCCCACCACCAGGCC | 84669 |
rs148425378 | snp | C/T | 0.000153988 | 0.00877328 | missense | USP32 | GRCh38.p7 | 17:60181607 | AAGTTCTCTTTACTA[C/T]TTGACAGTTTATTTT | 84669 |
rs148426945 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60363455 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs148454932 | in-del | -/A | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419851 | ATTATTATTATTATT[-/A]TTATTATTATTTTAT | 84669 |
rs148458839 | snp | A/G | 0.00185106 | 0.0303662 | synonymous-codon | USP32 | GRCh38.p7 | 17:60208706 | TGGCAAAGACAAAAA[A/G]TTGAAAGGGTCAAAT | 84669 |
rs148491672 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60233788 | CTTTATTTAGTAAAA[A/G]CACTTTTCTAATTAA | 84669 |
rs148493397 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60361762 | TATCCTGTCATTCAG[A/G]AGGTATAAATCTGGC | 84669 |
rs148514385 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409818 | AAAATACACTAACAC[C/T]AATGATAGCTCATAA | 84669 |
rs148522107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60292501 | GTGGTAATTCCATTC[A/C]TTTACTGAATCAGGC | 84669 |
rs148525964 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60206924 | CAAAATTCTTCTGCT[A/G]TAATATCCTCAGCAT | 84669 |
rs148528805 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60396237 | CATGCGCCACCACAC[C/T]TGACTAATTTTTTAT | 84669 |
rs148556588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259422 | AAATAAATTGTCCCA[C/G]TATGAGTGAGTGTGG | 84669 |
rs148561314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60346926 | AACCTAGAGAGGCAG[C/T]AAGACCAAGTCACAG | 84669 |
rs148578575 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60212967 | CATGTTGTCCAGGCT[A/G]GTCTGGAACTCCTGA | 84669 |
rs148606122 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60190027 | GGAGGTGGGGCCTAG[C/T]AGGAGGTGTTTGGGT | 84669 |
rs148679051 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | USP32 | GRCh38.p7 | 17:60332239 | GCCTGGGTGACAGAG[C/T]GAGATGCTGTCTCAA | 84669 |
rs148683559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60239892 | GAGCCTGCCACCAGG[C/T]CTGGCTAATTTTTGT | 84669 |
rs148698043 | in-del | -/CTCA | 0.084364 | 0.187256 | intron-variant | USP32 | GRCh38.p7 | 17:60329503 | TTTTTGAGATGAGGT[-/CTCA]CTATGTTGCCCAGGC | 84669 |
rs148701433 | snp | A/C/G | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60384997 | CTGAGCCCAAGCTAA[A/C/G]CCATCACATCCCCTG | 84669 |
rs148720689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298152 | AAGTTTCCACCCCAA[A/C]GTAAACATGGGACAC | 84669 |
rs148730808 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60246881 | CCATTTTTAAATTGG[A/G]TTATTTGGTTTTTTG | 84669 |
rs148739092 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60372763 | GCAGGAGGATAACTT[A/G]AGCCCTTGAGCCCAA | 84669 |
rs148765949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60216337 | GTTAACTACTCCGCC[A/G]AAAATCTAGACAAAA | 84669 |
rs148775472 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407695 | GCTGAGGCAGAAGAA[C/T]TGCTTGAACCCAGGA | 84669 |
rs148779486 | in-del | -/T | 0.104859 | 0.203554 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305175 | TATAAAGAAAAGAGG[-/T]TTTTTTTGGCTCACG | 84669 |
rs148789404 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60180058 | TGAGACAGAGTCTTG[C/T]TCTGTTGCCCAGGCT | 84669 |
rs148828035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411489 | TTACACTCTAGCCTC[A/G]GTGACAAAGTGAGAG | 84669 |
rs148834804 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60271582 | ATATATTTTAGTTTC[A/T]CAATTCAATTGCTAA | 84669 |
rs148847752 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295199 | CCTGCGTACAAAATA[C/T]AAGATGTTCACTGAA | 84669 |
rs148865292 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | USP32 | GRCh38.p7 | 17:60381417 | CTGCACTCCAGCTAG[A/G]GTGACAGAGGGAGAC | 84669 |
rs148882230 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | USP32 | GRCh38.p7 | 17:60262191 | GTTTTATGTATGTAT[C/G]TATGTATTTATTTAT | 84669 |
rs148891996 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | USP32 | GRCh38.p7 | 17:60215023 | GCCAGACTAGAGTGC[A/G]GTGCTGTGATTTTGG | 84669 |
rs148916973 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60388193 | TAAGAGCAATATAAA[C/T]GCCAGATTTTAAAGA | 84669 |
rs148934217 | snp | A/G | 0.000181239 | 0.00951769 | synonymous-codon | USP32 | GRCh38.p7 | 17:60190590 | TGTTTGATAGCGAAG[A/G]TGAAGGGCTGTGGGA | 84669 |
rs148961936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60279181 | CTGTACCTTTAGTAC[A/G]AACGGCTTTAAAGAT | 84669 |
rs148987140 | snp | A/G | 4.94222e-05 | 0.00497078 | synonymous-codon | USP32 | GRCh38.p7 | 17:60219674 | GCTCATCATACCCAT[A/G]TTCACCCAGATGTTA | 84669 |
rs149003273 | in-del | -/C | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295757 | ATTGTTATAATATTA[-/C]TATTTTATTATTGTT | 84669 |
rs149016469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317124 | TCCATGTAAATTTGA[A/G]AAAAATGGAGTGATG | 84669 |
rs149054239 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60340052 | ACCAAGAATAATGAT[A/G]CTCTGTTTACTCAGA | 84669 |
rs149073788 | snp | A/C | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422027 | GTACCCAGCACCCAG[A/C]ACCCAGCACGGAGGG | 84669 |
rs149085831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60307759 | CTCCTGCCTTGGTGC[A/C]CAAATGTTGCATTTT | 84669 |
rs149100110 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60182015 | AAAGATGATTTATGT[C/T]AGATTCAGTTGAAAA | 84669 |
rs149108882 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60257761 | GGTGCTGGGGTTACA[C/G]AGGTGAGAGCCACCA | 84669 |
rs149127429 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60364105 | AGATCAAAGTACCAG[C/G]AGATTCAGTGTCTGG | 84669 |
rs149139263 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP32 | GRCh38.p7 | 17:60314027 | TATGCTCAAGAATTT[A/G]AACAAAAATAAAAAC | 84669 |
rs149157181 | in-del | -/AC | 0.0854556 | 0.188216 | intron-variant | USP32 | GRCh38.p7 | 17:60300372 | TCTATATCCCACGAA[-/AC]ACAGACGGACACTAA | 84669 |
rs149208274 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60289168 | ACCCACCACCACGCC[C/T]GGCTAATTTTTTGTA | 84669 |
rs149211434 | in-del | -/A | 0.029116 | 0.117091 | intron-variant | USP32 | GRCh38.p7 | 17:60382530 | AGGGAGGGAAGCATT[-/A]AGCCATGGAATATAA | 84669 |
rs149235150 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | USP32 | GRCh38.p7 | 17:60285875 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 84669 |
rs149236868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390643 | AGGTGATGGTCAACT[G/T]AACTTACCCACTTAC | 84669 |
rs149244340 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon | USP32 | GRCh38.p7 | 17:60180614 | AGTGACGTAATGGCC[C/T]CCACCCAGAATTCCT | 84669 |
rs149309118 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60380110 | GATTTAGGCAAAGTC[A/C]AGAAGGATAGACAGA | 84669 |
rs149317573 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60337694 | CCAGCCTAGGCAATA[C/T]GGTGAGACCCCGTCT | 84669 |
rs149321191 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405394 | TATTGTAGTAGAGAT[G/T]GGGTTTCACCGTGTT | 84669 |
rs149353990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60191787 | GTGCTGGGATTACAC[A/G]CGTGAGCCACCACGC | 84669 |
rs149356926 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60268957 | GATTTAATAATGGAA[C/T]GTATTTATGCTTACA | 84669 |
rs149376161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60341225 | GCCTGCCTTGCTAGG[A/T]TGGGGAAGTTCTCCT | 84669 |
rs149386197 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60205990 | CCTTTGAAGACACTG[C/T]CCAATACAGTAACCT | 84669 |
rs149394391 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60323727 | TACTGCTCCTATAAG[G/T]CTTTTTATATCTCAC | 84669 |
rs149406881 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60309965 | AGGAGAACTGTTTGA[A/G]CCTGGGAGGTGGAGG | 84669 |
rs149450659 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60365932 | TATGTGGGGTTTTTC[A/G]GTTCATTTTTGGTTT | 84669 |
rs149459704 | snp | A/C/G | 1.64795e-05 | 0.00287045 | missense | USP32 | GRCh38.p7 | 17:60205641 | ACATTTCATTTGTAG[A/C/G]TGGCGAAGAGGAGAA | 84669 |
rs149491602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232942 | ATCTGCCAGGCACTG[G/T]GCTAAGTGCTTCACA | 84669 |
rs149513018 | snp | C/T | 0.000148245 | 0.00860815 | missense | USP32 | GRCh38.p7 | 17:60226111 | CTTCTGTAGTATTCA[C/T]GTAACTGAGGCTGCT | 84669 |
rs149518519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408826 | ACCAAGGAGCAGAGA[C/T]GGAACTAAGTGGACA | 84669 |
rs149535647 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60291991 | TAGTATCCTACACCA[C/G]CAATTTTTTAATTCC | 84669 |
rs149566071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60346032 | AATTGGCAAGCATTA[C/T]ACTTCTTTTTTGGTT | 84669 |
rs149568143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60222843 | CACGTCACCATGCCC[A/G]GCTAATTTTTGTATT | 84669 |
rs149570008 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414452 | TTTATTTTTTGAGAC[A/T]GAGTCTCGCTCTGTT | 84669 |
rs149577741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60189047 | TAAAAAGGGGAAGAG[A/G]TTTATAGAGCCAAAT | 84669 |
rs149588621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60297766 | ATGGCATGAGCCACC[A/G]TGCCTGGCCATTTTT | 84669 |
rs149607440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60383545 | AAGGCTGTACACAAA[C/T]TGTTCAGAATATTGC | 84669 |
rs149621084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229254 | TATGTTACCCAGACT[C/G]GTCTCAAACTCCTGG | 84669 |
rs149623738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353318 | CTTGCTGGAACCCAA[C/T]GTTATTTCCAATGGG | 84669 |
rs149627489 | in-del | -/GAACATAG | 0.0123036 | 0.0774623 | intron-variant | USP32 | GRCh38.p7 | 17:60261115 | GGGAGAAGCTATGTT[-/GAACATAG]GCTATATTTCAAAAT | 84669 |
rs149668827 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60273821 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGTGCCT | 84669 |
rs149687746 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60255488 | GTTTTTCAGTAGAAA[C/T]GGGGTTTCACTATGT | 84669 |
rs149695770 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60343024 | TCACGCTGGGAGCTG[C/T]AGACCAGAGCTGTTC | 84669 |
rs149710296 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP32 | GRCh38.p7 | 17:60395210 | GTAAAGTAAGATTTA[C/T]AGCAGTACTAACATG | 84669 |
rs149731162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312102 | CTTTCTGGGCCTTAG[C/T]TGCAGTCCATGACAC | 84669 |
rs149762901 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60216137 | CGACAGACATGACCT[C/T]GAATTCCTGAAGGGC | 84669 |
rs149764035 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60242177 | AGGTGGCTATTCACA[A/C/G]GTGTGATCACTGCAT | 84669 |
rs149767106 | snp | C/T | 1.64882e-05 | 0.00287121 | missense | USP32 | GRCh38.p7 | 17:60185516 | CTAAGCAGTGGGTCT[C/T]ACACTTGGAACAGTA | 84669 |
rs149774169 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP32 | GRCh38.p7 | 17:60200137 | AGGCATAGAGTACAG[C/T]GAGCCGAGATCGTGC | 84669 |
rs149817202 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | USP32 | GRCh38.p7 | 17:60249310 | TCAACTAGGGAAGAA[A/T]AAAGTGCTAAAGCCC | 84669 |
rs149879224 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60225733 | CCGAGGCAGGCAGAT[C/T]ACGAGGTTGGGAGTT | 84669 |
rs149888560 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | USP32 | GRCh38.p7 | 17:60315307 | CAGGAGGCTGAGGCA[G/T]GAGAATGGCTTGAAC | 84669 |
rs149900581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301031 | TCAGTACTTTATTCC[G/T]TTTTATACCAGAATA | 84669 |
rs149923051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60282432 | AATCTCGGCTCACTG[C/T]AACCTCTGCCTCCCA | 84669 |
rs149923342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60371720 | AACTGAAAGACTGAC[A/C]ATATGAAGCACCAGT | 84669 |
rs149937692 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60356459 | AAGCAGAGTTGCAAA[C/G]TGACTGTACAACATT | 84669 |
rs150011833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402827 | GGGACTGGAATCCTC[C/T]GAAGGCTTTCTCACT | 84669 |
rs150047706 | snp | A/T | 3.30611e-05 | 0.00406565 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269490 | CCTGCAACAGGCTGA[A/T]AACCCACAGGATATC | 84669 |
rs150057997 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60339289 | TGCACATAAGTGCTA[A/C]AAGGTATAAATGGCC | 84669 |
rs150063131 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407219 | AAAATTCCAAAAAGG[A/C]AGAAGGTATGCAAAA | 84669 |
rs150075671 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60244697 | AGAGCAGGCGTTCCA[C/T]CTCAGCTTACTGCAA | 84669 |
rs150162791 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60260755 | AATTATTGCATAATC[A/G/T]CTTATACAGTATTAT | 84669 |
rs150166514 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60187793 | ACCTCTTGGGATCTA[C/T]GCTTAGATCCTCTAC | 84669 |
rs150183974 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | USP32 | GRCh38.p7 | 17:60367018 | AGTTTTAGTAGAGAC[G/T]GGGTTTCACCGTGTT | 84669 |
rs150203053 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60228750 | GATGGCCTCAACCCA[C/G]GGGGTGGAGGTTGAA | 84669 |
rs150205652 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60316603 | CTCAACACTTTGGGA[A/G]GCTGAGACAGGGGGA | 84669 |
rs150213029 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60191123 | AAAGTTTACAGGGGC[C/T]GGGCATGGTGGCTCA | 84669 |
rs150224191 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60303125 | ACTCAACCCAGCAAA[A/T]ACTAGCCAAAGGAAA | 84669 |
rs150225214 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378625 | AAAAGAAATTAAATT[A/C]TGCTATGTACTACAA | 84669 |
rs150233863 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60284973 | AAATCCCCACTTGTC[A/G]TTGTTATATTGAGAG | 84669 |
rs150255904 | snp | C/T | 0.0383715 | 0.133092 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232295 | CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGGAAC | 84669 |
rs150260302 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422978 | TAGGACCTGGAGGAG[C/G]CTGTGTCCCATCTCC | 84669 |
rs150286225 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | USP32 | GRCh38.p7 | 17:60290883 | AAGATGTCTAGGGGT[C/T]AGTTTTGTGGAACTA | 84669 |
rs150330152 | snp | C/T | 0 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403665 | AAGGAAAGGGGGTCG[C/T]GATGTATTGAACTTA | 84669 |
rs150372806 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | USP32 | GRCh38.p7 | 17:60307173 | GGCTCGATCTTGGCT[C/T]TCTGCAAACTCAACC | 84669 |
rs150377528 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60340631 | TTTATCCAATTTGCC[A/C]ATCTGTGCCTTTTAA | 84669 |
rs150381975 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408673 | ATGAGCCACCATGCC[C/T]GGCCAATCTGGCTCA | 84669 |
rs150398988 | snp | A/C | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393775 | CCGCAACCTCTGCCT[A/C]TCTGGTTCAAGCGAC | 84669 |
rs150415095 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | USP32 | GRCh38.p7 | 17:60363281 | GCAACACGATGAAAC[C/G]CCGTCTCTACTAAAA | 84669 |
rs150429593 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60345720 | GGCACAGTGGCTCAC[G/T]CCTATAATCCCAGTA | 84669 |
rs150445172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330397 | TGGATCTTCTATTCT[C/T]AGTAATCTCATTCTG | 84669 |
rs150468918 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60280379 | TGGGATTACAGGCTC[G/T]GGCTACTGCACCTGG | 84669 |
rs150487350 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | USP32 | GRCh38.p7 | 17:60198382 | ACATGGAACAATCAA[C/T]GGCATTCCAAAGAGG | 84669 |
rs150520954 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | USP32 | GRCh38.p7 | 17:60201652 | ACTGATTACTAGTGT[C/T]GTTGATCATTTTTTT | 84669 |
rs150525264 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60390382 | AGCCATTGCCTAATT[C/G]AGGCCAGACCTGTCA | 84669 |
rs150529055 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419320 | CTAAATGATGAGAAC[A/G]CATGAACACGTAGAG | 84669 |
rs150537662 | in-del | -/AAC | 0.263535 | 0.249633 | intron-variant | USP32 | GRCh38.p7 | 17:60219191 | TTTGCCAAAAAACCA[-/AAC]AACAACAAAAACCTT | 84669 |
rs150551007 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60253536 | TTTGGGAGGCTGAGG[C/G]GGGCAGATCACTTGA | 84669 |
rs150570702 | snp | C/T | 3.295e-05 | 0.00405881 | missense | USP32 | GRCh38.p7 | 17:60345569 | AGTCCACAGGTCCTC[C/T]TGAAAGCATCCTTCA | 84669 |
rs150572054 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60325233 | AGCCTGGCCAACATG[A/G]TGAAACCCTGTCTCT | 84669 |
rs150592297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194777 | GCAACCACCACCTCC[C/T]ATCTTTTTGGGTTAC | 84669 |
rs150612998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60293288 | AATGTCTGCATAAAC[C/T]GTATTAAAATGAAAA | 84669 |
rs150677509 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | USP32 | GRCh38.p7 | 17:60360128 | CTGCCTCAGCCTCCT[A/G]AAGTGCTGGGATTAC | 84669 |
rs150698699 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60309375 | GAGGCTGACACAGGC[G/T]GATAACTTGAGCTCA | 84669 |
rs150701747 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410388 | AAAAACCCTAGCCTC[A/G]GTGGGCGCGGTGGCT | 84669 |
rs150726565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60276817 | TGATCAGATTGGTCA[C/T]GGTCACCAGTGAAAA | 84669 |
rs150750020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225207 | CCTGTAATCCCAGCA[C/T]TTTGAGAGGCTGAGG | 84669 |
rs150753508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415829 | GATATGCTTGGTGGT[A/G]TTTTTTTTGTTTATT | 84669 |
rs150758833 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60211663 | GTCTCTGAAATGCTA[C/G]AGAAGGCTTTTCATG | 84669 |
rs150770135 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60333536 | ACCCGGGAGGTGGAG[A/G]TTACAGTGAGCCAAG | 84669 |
rs150771203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402574 | GTTATTCTTCTGAAA[C/T]GCTAAATTAGTAATC | 84669 |
rs150784651 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60198803 | TTAAACAATTAAGGC[C/T]CTTTCTTTCTCCAGA | 84669 |
rs150812249 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | USP32 | GRCh38.p7 | 17:60215584 | ACTTTCCTAAACTTT[A/C]TTTGAATCACTAATC | 84669 |
rs150821486 | snp | A/G/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60247779 | ACCTCCACCTCCCCA[A/G/T]TTCAAGCGATTCTCC | 84669 |
rs150823981 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60339115 | GGGGTTTCACCATGT[C/T]GGCCAGGCTGGTCAC | 84669 |
rs150894577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60382127 | CATAGTGAGATAAGC[A/T]CACCGGCAAACTGCC | 84669 |
rs150909700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265148 | AGAAATACAGATGAT[A/G]GGCTATAGTTGCCAA | 84669 |
rs150921213 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP32 | GRCh38.p7 | 17:60187456 | CAAGGAAAAAACTGA[C/T]GTGCTTCAAAAGGAA | 84669 |
rs150958664 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306407 | CTTTGGAAAGCCGAG[C/G]GGGGTGGATCATTTG | 84669 |
rs150998458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362163 | ACTACTTCTGTTCCC[C/T]CAGCATCCCTGAGCT | 84669 |
rs151002997 | in-del | -/TAT | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419829 | AAAAATTATTATTAT[-/TAT]TATTATTATTATTAT | 84669 |
rs151012034 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60311813 | CTGGGCAACAAGAGC[A/G]AAATTCCACCTCAAA | 84669 |
rs151016613 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60222152 | TCTTCCCCTCCAGCC[G/T]AAGTTCCACATATCC | 84669 |
rs151016809 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411903 | GATGGACACTTGGGT[C/T]GTTTCCACTTTTTGG | 84669 |
rs151033815 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | USP32 | GRCh38.p7 | 17:60398387 | GCAACAGAGTGAGAC[C/T]TTGCCTCAAAAAAAG | 84669 |
rs151050590 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366984 | GCCCGCCACCACACC[C/T]AGCTAATTTTGTTTT | 84669 |
rs151053350 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | USP32 | GRCh38.p7 | 17:60279613 | AGGCTGAGGCAGGTA[C/G]ATCACTAGAGCCCAG | 84669 |
rs151073979 | in-del | -/T | 0.084364 | 0.187256 | intron-variant | USP32 | GRCh38.p7 | 17:60242787 | TTGATTAATGTATCC[-/T]TAGGTAAATTGTGAA | 84669 |
rs151079186 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60213926 | TGGTGTTTGGTTACA[C/T]GAATACGTTTTGTTT | 84669 |
rs151088622 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60300455 | CATTATAGCATTTCC[C/T]TGATCAGCAGGATTT | 84669 |
rs151092952 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403432 | GGTGAAATAATATCC[A/G]GAAATGTTGTCATGC | 84669 |
rs151127410 | in-del | -/A | 0.0916144 | 0.193427 | intron-variant | USP32 | GRCh38.p7 | 17:60310045 | AAGACTCCATCAAGG[-/A]AAAAAAAAAAGAAAG | 84669 |
rs151158730 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60234117 | ACCAAGCATGACTAA[-/T]TTTTTTTTTTTTTTT | 84669 |
rs151173705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347828 | ACAGAGAATGTAAGA[A/G]TAAGTCAGGAAAGGC | 84669 |
rs151208872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60385946 | AAGGTCTTGAATTCT[C/G]GTCATCTTTGAATAG | 84669 |
rs151225579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355708 | AAAATTGGTGGCACA[C/T]GCCTGTAGTCTCAAC | 84669 |
rs151265987 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60321036 | AGTATATGGCACAGT[A/C]GTATAACTAAAAACC | 84669 |
rs151266227 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP32 | GRCh38.p7 | 17:60196537 | TTTATTTAAATAACT[C/T]ATTTTGGCCGGGCAC | 84669 |
rs151275525 | snp | C/T | 8.23757e-05 | 0.00641725 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266029 | AAAGTGCAACCACCA[C/T]GTCTCTCAGTTCAAC | 84669 |
rs151298104 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60254936 | ATTCTCTATATGTCT[A/G]TGTACTGCTCTATAA | 84669 |
rs151298270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375544 | CCCATGAAGTGTACA[A/G]ACAATACATACTAAA | 84669 |
rs151309518 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60238465 | TTGAGCCCAGGAGTT[C/T]AAGACCAGCCTGGGC | 84669 |
rs151318641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330068 | GCTTCCTTTAAAGCA[A/G]TATTTGTCCCTACTC | 84669 |
rs180672251 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60262121 | TACTGCTAAGCAAGG[A/T]ATCATATGAACTTTT | 84669 |
rs180676536 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60307012 | AGGAAAACTATAAAA[C/T]ACTGATGAAAGAAAT | 84669 |
rs180682988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60282962 | CTTGCAACTTGTGGG[G/T]GTAAACAAAATCATT | 84669 |
rs180685118 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60269618 | ATGTTAATAATGACA[A/T]GTTTACAAAAGGAGG | 84669 |
rs180695070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60292571 | AGTCCATAATCAATA[C/T]GAGAAAAAATTCTAG | 84669 |
rs180695881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60241625 | CATTGTGCTTTTAAT[C/T]TGCCTTCTCTGAGGA | 84669 |
rs180709456 | snp | A/G | 0.000330825 | 0.012857 | synonymous-codon | USP32 | GRCh38.p7 | 17:60301687 | TTTGGATGTTCCACC[A/G]AAAGAACAGTAAATC | 84669 |
rs180709491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318329 | TTTAGGCTAATACAA[C/T]TTTATGCTGAATGGT | 84669 |
rs180712640 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60358739 | CATAGATCTAATTTT[G/T]AGAAACTAGATGAGA | 84669 |
rs180714543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326344 | AGACAGAGTTTCGCT[C/T]TCGTCGCCCCGGCTC | 84669 |
rs180720289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60335850 | TGCAACATGTATAAC[A/C]AAATTCTGATTAAGT | 84669 |
rs180729198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381565 | CATTTTACTCAGGTG[C/T]TCTTCTTCAGTGGAA | 84669 |
rs180733647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400316 | GTTGAAAGTGGACTG[G/T]AGTGAGAGGAGAAGG | 84669 |
rs180736296 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420458 | AGATCACCTGAAGTC[A/G]GGAGTTAGACACCAG | 84669 |
rs180839647 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60198845 | TAAGCTGGGTGTGGT[A/G]GCTCACGCCTGTAAT | 84669 |
rs180839949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60205140 | CAGATGCACTGACTA[C/T]CCTGTTGCCTCTTAA | 84669 |
rs180840072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60189254 | TTATACTTATTTCTG[A/G]CTAGAAAGGGCTCCC | 84669 |
rs180857027 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60251062 | ATCCTCCCACCTCAG[A/C]CTCCCAAGTAGCTGG | 84669 |
rs180873243 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60221562 | CAGGCAGGAGTGCAA[C/T]GGTGTGCAGTCTTGG | 84669 |
rs180881146 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232329 | AGGCACACGCCACCA[C/T]GCCAGGCTAATTTTT | 84669 |
rs180893491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237450 | GAGGTGAAAATGGCA[C/T]AATATGAAATTATTT | 84669 |
rs180894014 | snp | C/T | 6.61452e-05 | 0.0057505 | intron-variant | USP32 | GRCh38.p7 | 17:60180511 | CTGTTGATATTCTGT[C/T]TCTAACTTTCATTCA | 84669 |
rs180895589 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60185281 | TAGGAAAAAGAACTA[C/T]AAAATATTTGTAGAA | 84669 |
rs180896740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214399 | GTAACTTAAAAGATG[A/G]ACTTTTCACTGATAT | 84669 |
rs180905112 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265599 | GATGGGGTCTCCTTA[C/T]GTTGCCCAGGATTAT | 84669 |
rs180906157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196197 | GCTTGAACCTGGGAG[A/G]CAGAGGTGCAGTGAG | 84669 |
rs180920174 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60279133 | ATCATCATCGAGATG[A/C]TCAGCATCATCACAA | 84669 |
rs180929821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60321809 | TTAACAGTGACCATT[C/T]GTTGTGATGGTCAAC | 84669 |
rs180932053 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60226981 | CCCGGGAGGTTGCAG[G/T]AAGCTGAGATTGCGC | 84669 |
rs180934653 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60257329 | ACTTCGTGGATCACA[C/T]GTGCCAATTGGGGGG | 84669 |
rs180938954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60201583 | TCAGTCTGTTTAATT[C/T]TACCTGTTCAGGTGA | 84669 |
rs180964559 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60304565 | TGAAAGATTAACTAG[C/T]AGTCTACATCAGTAA | 84669 |
rs180978146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244193 | GGCGCCCACCACCAC[A/G]CCCAGCTAATTTTTT | 84669 |
rs180989335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60286584 | TGCATGGAAATAAAG[A/G]ATACTCCTGAGTTCC | 84669 |
rs181103459 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60313759 | CTCACCATTACAAAG[C/T]TTTAACACAGGATTA | 84669 |
rs181103515 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60361622 | ATTGTGCTTTTCCTA[A/C/G]CCTCTTGTTCACTAT | 84669 |
rs181109788 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60338979 | CAGTGACGTGATCTT[A/G/T]GCTGATTGCAACCTC | 84669 |
rs181110013 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60297895 | CCTGTTCCACAAGCC[A/G]TAACTACAGCTTTGA | 84669 |
rs181116244 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60384852 | GTGGCTCACGCCTGT[A/G]ATTCCAGCATTTTGG | 84669 |
rs181214599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60376021 | CACTGTCACTCAATC[C/T]TTTGCCAATTATAAT | 84669 |
rs181234218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60352217 | AGAAATGACTGGGGG[A/G]ACCTCCATGAAGGCT | 84669 |
rs181234660 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414219 | AATACAAAAATTAGC[G/T]AGGCATGGTGGCATA | 84669 |
rs181240926 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60394880 | TCCTGGGTAGCTGGG[A/G]TTATAGGCGCACACC | 84669 |
rs181283635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388802 | GTCTAGCTAAAATAG[C/T]GTGCAAAAACCAATC | 84669 |
rs181283798 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | USP32 | GRCh38.p7 | 17:60220788 | AGCTGGGAATACAGG[A/C]GCCCGCCACCACGCC | 84669 |
rs181287061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369755 | TCTACACAATGATTT[G/T]TTTTTAAGAGACAGG | 84669 |
rs181305172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60282474 | TTCTCCTGCCTCAGC[A/G]TCCAAGGTAGCTGGG | 84669 |
rs181311517 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60240897 | TGACGAATAACCCTG[C/G]CTGCCTTTCCATCCT | 84669 |
rs181312879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60261823 | AATCTGATTCTTTTA[C/T]ATAACCACAAATATT | 84669 |
rs181316786 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60318204 | AAAGCAACAAAATTA[A/C]ATTTAATCTATTTAA | 84669 |
rs181328488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301188 | TGTGTGGTAAACATA[C/T]GTATTAAATTTTCTT | 84669 |
rs181371384 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418670 | TACATTTACAAGAAT[A/C]AAAACAAACAACCCC | 84669 |
rs181396383 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60179629 | GGAAAATATTTTGAC[C/T]ATAGACAAGTCAAAA | 84669 |
rs181417242 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | USP32 | GRCh38.p7 | 17:60209255 | GAAATTCATTCATTT[C/T]TGCAGTAAAGTTCTG | 84669 |
rs181427749 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60293720 | CCAGATACATGCAAA[G/T]GCTGAAATATGGACA | 84669 |
rs181430246 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60346337 | ACAAATATTTCAAAT[A/T]AGCAGGTAAGCTAAA | 84669 |
rs181436686 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60252312 | TAAAATAGGACATGC[G/T]GTTCCTCAGTAACCA | 84669 |
rs181442960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60328524 | CCTCACCCTCCATCT[A/G]CATACCTCATTCTTC | 84669 |
rs181455353 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | USP32 | GRCh38.p7 | 17:60357918 | GGATTACAGGCATGT[A/G]CCACCACACCCAGCT | 84669 |
rs181463879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305798 | TAAGGAAGAAATTTT[A/G]AGTAAGGTATGACTT | 84669 |
rs181465101 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60399502 | TCTACAAAAAAATTT[A/T]AAAAAAAAAATTTAG | 84669 |
rs181474141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60266613 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 84669 |
rs181478817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60289101 | CAAGCTCTGCCTCCC[A/G]GGTTCACGCCATTCT | 84669 |
rs181489734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60279067 | TAACTTATTTCAAAC[C/T]TTTAATTACATAGAA | 84669 |
rs181490851 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60323503 | TGACTGTTAAAGTAA[A/G]GTTTCTTTTTGGGGA | 84669 |
rs181491206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375501 | GTTAGAATTTTCACT[A/G]TAAAACCAAACACGT | 84669 |
rs181492778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60363329 | GCGTAGCGGCGTGCA[C/T]CTGTAGTCCCAACTA | 84669 |
rs181496320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60312137 | GTTGAAGCAATGTGC[C/T]AAGTCGTCTCATTCC | 84669 |
rs181497896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413512 | GGTGGATTAAAAAAA[A/T]TTTGATTTCTAATTG | 84669 |
rs181499818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60394385 | ATGGCCTTGCTATAC[A/C]AGGGATAGGCTTGGG | 84669 |
rs181501277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60340087 | AAGGTCCAAGCTCTC[C/T]ATAGGATTTTTTTTT | 84669 |
rs181501833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60351183 | GGTTCAAAGTCTATG[A/G]GGAGTAGTTAGACTC | 84669 |
rs181524325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234094 | AGCTGGGACTACAGG[C/T]GCACACTACCAAGCA | 84669 |
rs181551422 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60195436 | TCCACCTACAGGGTT[A/G]AAGCAATTCTCAGGC | 84669 |
rs181554413 | snp | A/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178966 | ATCTGGACAAGCACA[A/T]TTGAATTCTTATTTG | 84669 |
rs181565157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60385419 | AGTGTGGTGGCACAC[A/G]CCTGTAGTCCCAGCT | 84669 |
rs181573741 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60334344 | AAATTTTATGGTAGT[A/C]CCTGATAAAATAAAC | 84669 |
rs181580552 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60197409 | TGGAAGTTTGAGAAC[A/G]GCCTGACCAACATGA | 84669 |
rs181595363 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60308549 | ATCCACTCATCTTCA[C/T]GAAAAAGCACAAAGA | 84669 |
rs181598559 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | USP32 | GRCh38.p7 | 17:60381428 | CTAGGGTGACAGAGG[A/G]AGACCCTGTCTCAAA | 84669 |
rs181609745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297597 | GGGATTACAGTCACA[C/T]GCCCAGCTAATTTTT | 84669 |
rs181612868 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60256325 | GAGGGGTAGGCAAAT[A/C]ACTAGATTATGACTA | 84669 |
rs181641188 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60331688 | GCCAAGGTGGGAGGA[C/T]TGCTTGAGTCCAGGA | 84669 |
rs181650190 | snp | C/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60251706 | TTTTTAAATATAATC[C/T]GGATATTTGATCTTA | 84669 |
rs181660205 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60292913 | CATTTCCTACCACTC[C/T]CTTGTTCACACCATT | 84669 |
rs181668250 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60307430 | TGAAATGACAATACT[A/G]TCCACAGCAATTTAC | 84669 |
rs181672389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271102 | ACAACCACTGCCTTG[G/T]TCAAACACATTTTAT | 84669 |
rs181702425 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403209 | TAGAGACAGGGACAG[G/T]GTTTCACCATGTTGG | 84669 |
rs181713430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236367 | ATTAGGAGAGACTGC[A/C]AAAACCCAATTAGTA | 84669 |
rs181745383 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60191754 | GACCTCTTGATCTGC[C/T]CGCCTCCACCTCCCA | 84669 |
rs181771834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233497 | ACAAAACACTTAACA[A/T]GCATCAAACTCATTT | 84669 |
rs181844213 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60326908 | CAGTTCTCAGTCTTA[C/T]GTAGATGCTAAAAAA | 84669 |
rs181847208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400413 | GCGGTGAGAGGTTAG[A/G]TCCCAGATATTATTT | 84669 |
rs181849960 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421971 | CCCGTAGGCACTGGC[A/G]GGGATCTTTATACAC | 84669 |
rs181869999 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60345945 | CAAGACCATGCCGCC[A/G]CACTCCAGCATGGAC | 84669 |
rs181874752 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60214144 | ACAGGGTTTCACCAC[A/G]TTGGCCAGGCTGGTC | 84669 |
rs181892690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60395305 | TCCATGGATTAAGCA[C/T]TTCTAAAAATTGTGA | 84669 |
rs181902367 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415259 | GACTTCACTGTACAT[A/G]GTCAAATATCTTACT | 84669 |
rs181998479 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60202302 | ATGACATTATTTTAA[A/G]TATCATATCTTTGTG | 84669 |
rs182004835 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60255773 | ATATGGTTGGTAAAA[C/T]TCACTAAATATCTCT | 84669 |
rs182004963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185833 | TTAGGAGGCCGAGGT[A/G]GGGTAATTGCTTGAG | 84669 |
rs182030058 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60336143 | ACTTAGAACATCCAT[A/C]ATCTATGTAATGTTC | 84669 |
rs182032045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227838 | ACTGCTTCACTTTAG[C/T]AGCCAAAAAATTTTT | 84669 |
rs182036979 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60278269 | AAACGTATTATATGC[C/T]TGACATTGTACTAAA | 84669 |
rs182037770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408440 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 84669 |
rs182037994 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60381820 | CAAGGAATTATCCTG[C/T]AAAATTAAGATACAG | 84669 |
rs182047468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60210374 | TGGAGTACAGTGGTG[C/T]GATCTTGGCTCATTG | 84669 |
rs182050119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234718 | CTGGGCGACAAAAGC[A/G]AGACTCCGTCTCAGA | 84669 |
rs182053068 | snp | A/G | 0.00143204 | 0.0267202 | intron-variant | USP32 | GRCh38.p7 | 17:60205401 | ATGACTATTTCACAA[A/G]TGACACTAGCAAGAC | 84669 |
rs182060907 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60192478 | TTCGCTCTTGTTGCC[C/T]GGCTGGAGTGCAGTG | 84669 |
rs182063217 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60273161 | TATTTTTAGTAGAGA[C/T]GGAGTTTCGCCGTAT | 84669 |
rs182071714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60294202 | TGAGCCACCTTGCCT[A/G]GCCCAAAGATGACAA | 84669 |
rs182074360 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60252734 | ACCTCAGGAACAGAT[C/T]TCAGAATAATTCTTC | 84669 |
rs182136229 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403110 | TCCACCTCCCGGGTT[C/T]AAATGATTCTCCTGC | 84669 |
rs182159446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60320934 | ATGGTCCTAGGAGAA[C/T]GGGACAAATTCTCAT | 84669 |
rs182169547 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60360375 | TGTATTTGTATTTTG[G/T]ATTACAGGCGCAGTG | 84669 |
rs182174803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60338281 | AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAG | 84669 |
rs182228559 | snp | C/G | 0.0770498 | 0.180522 | intron-variant | USP32 | GRCh38.p7 | 17:60213133 | AAAAAGTTTTTAATG[C/G]CATGTGCATGCCAGT | 84669 |
rs182268181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194858 | CTCCAATCACTGCCC[C/T]GAAATCCTCACTTGC | 84669 |
rs182299584 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60319264 | TTTTATATATTTTGC[C/G]ACAACAAAAATTTTA | 84669 |
rs182301071 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60322116 | TAAGATGTGTTTAAC[A/G]TAAGACTCAACATGC | 84669 |
rs182309702 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388276 | TAAGAATCATTTTAA[G/T]TCAGCCGATTCTTAC | 84669 |
rs182311129 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60288063 | AGATTGCAGTGAGCC[A/G]AGATCACACCACTGT | 84669 |
rs182328133 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60359204 | TGTCCCTCCTACAAA[A/G]TAACTTTCCTTATAA | 84669 |
rs182342659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362701 | AGTTTATTCATTTGC[C/T]TCCAGCAGTTTCTCG | 84669 |
rs182382066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60382610 | ATTTAAAATCACCTG[A/G]ATTATTTAGAACCAA | 84669 |
rs182386056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60243166 | CTTTCAAATTATTCT[A/G]TCTAGTACATGACAA | 84669 |
rs182401287 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60200470 | GAGGCTGAGGCAGGA[A/G]AATCACTTGAACACA | 84669 |
rs182402161 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60401045 | CCTATAGTCCCAGCT[A/G]CTTAGGAGGCTGTGG | 84669 |
rs182402804 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60385114 | ACATTCCACCATTGT[A/G]ATTTATTCCTGTCCC | 84669 |
rs182411056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60284622 | GCCATTTTTAACATA[C/T]TGAAAATTATTTGAC | 84669 |
rs182413880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423755 | ACAGGCGTGAGCCAC[A/T]GGGCCTGGCCTAATT | 84669 |
rs182414798 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60309438 | AAACCCCTGTCTCTA[A/C]AAAAAATACAAAAAT | 84669 |
rs182436979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347644 | AGGCGTGAGCCACCG[C/T]GCCCGGCCTACACCT | 84669 |
rs182467584 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60389621 | TTACTAAATGGACCA[C/T]GCTTAAAGAAGGGGG | 84669 |
rs182489186 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60235850 | CCTCACAAGGGTGGT[A/G]CGAGAAATAAATGAG | 84669 |
rs182548991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305285 | AAAGTGAAGGGGGAG[C/G]AGAGAACAAGCATGT | 84669 |
rs182570148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60372415 | TATGGGATGGCCTAT[C/T]ACTCCTAGGCTACAA | 84669 |
rs182578482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60391235 | GAAACCTAAGACAAG[A/G]TCTGGTGCCAACGCC | 84669 |
rs182578559 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411272 | GAGGTTGCGGTGAGC[A/C]GAGATTGCCCGATTG | 84669 |
rs182584967 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60339240 | AATATTAAGTACACT[A/G]ATCTATCCTCAAAAC | 84669 |
rs182586254 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60239443 | CTCCTTTCCTAAGAT[A/T]CTTATGTTGACACAT | 84669 |
rs182592339 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60260644 | AAGATGCTTAGTAAA[C/T]ATTTTACTAAGTTTA | 84669 |
rs182605911 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60182822 | TTTTGATCCTCTAGA[A/C]CCCCTGAAAGATGGG | 84669 |
rs182609373 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60299982 | CTTATGATTAACCCT[C/T]ATGACCTAATCACCT | 84669 |
rs182619986 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60316302 | TAGTTCTGAACCCTA[C/G]ATTTTTTTTTCCCCA | 84669 |
rs182623460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60191877 | ACTTTAGTATCATTA[A/G]GCACTTTCCCTGTTG | 84669 |
rs182625753 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60341101 | TCTGGCTGCCCTTAA[C/T]ATTTTTTCCTTCATT | 84669 |
rs182625924 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60280810 | CAAAGACATCAATAG[G/T]GAATTGTTTAGCCAG | 84669 |
rs182627427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60186995 | CAGACCACAAGGCCC[A/G]CACTGACTGCCTCTC | 84669 |
rs182634606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60385598 | TATAATCTCAGCACT[C/T]TGGGAGGCCAGCGTA | 84669 |
rs182638423 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP32 | GRCh38.p7 | 17:60223665 | ATATGAACTCAATGC[C/T]CATGTATTGTATTAC | 84669 |
rs182639504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333525 | GAGTCACTTGAACCC[A/G]GGAGGTGGAGGTTAC | 84669 |
rs182643831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60364202 | CAGGCCTCTTTTAGA[A/G]GGGCACTAATCCCAT | 84669 |
rs182645890 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60229007 | CCATAAACATAAATG[C/T]CTTATTATTTAAATC | 84669 |
rs182647838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403818 | GCCAAGGCGGGAGTA[C/T]TGATTGAGCCCAGGA | 84669 |
rs182667329 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60303703 | ATATGAAGCACTTAT[C/G]TTTCAACCATAAATT | 84669 |
rs182677801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263332 | ACATCTAGATCTCTT[G/T]AGCCACTACAGAGTA | 84669 |
rs182678950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337705 | AATATGGTGAGACCC[C/T]GTCTCCACAAAAAAT | 84669 |
rs182682348 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60328940 | CCCTCCCCAGCTCCA[C/T]GCCTGACTCACGCAG | 84669 |
rs182688468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60319755 | ACTGCACTCCAGCCT[A/G]GATGACAGAGTGAGA | 84669 |
rs182689115 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60370719 | GTGAGTTGTGATCAC[A/G]CCACTATACTCCAGC | 84669 |
rs182811175 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60242894 | CTATACAATTTAGGA[A/C]TAGCTTGTCAATTTA | 84669 |
rs182833184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60303041 | TAGTCACCAAATTAT[A/G]TTTATAAATATATTT | 84669 |
rs182843030 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60262655 | GGCCCTTCAAGATAC[G/T]TCTCCAATCCAGGTC | 84669 |
rs182848090 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60284253 | AAGTCTCGCCCTGTC[A/G]CCCAGGCTGGAGTGT | 84669 |
rs182862736 | snp | A/C | 0.0020028 | 0.0315815 | intron-variant | USP32 | GRCh38.p7 | 17:60246711 | TCAGAATCAGTTATT[A/C]TTTGTCTTTTTTATA | 84669 |
rs182864138 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP32 | GRCh38.p7 | 17:60196706 | GGCGGGCACCTGTAA[C/T]CCCAGCTACTCAGGA | 84669 |
rs182867322 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177462 | TAATTTAATAAATTT[C/T]CTGCTAGTTCATGAA | 84669 |
rs182870679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228421 | TAAAGATAATATCAA[A/G]CTTCTCACAGCTTTT | 84669 |
rs182891736 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60215490 | TAGGACAGAGTTAAA[A/G]AAAAAAAAAACTCAG | 84669 |
rs182907492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60266950 | TGAGCCACTGTGCCC[A/G]GCCAATTTTTGTATT | 84669 |
rs182921270 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306193 | ATTACTAATTAGCTT[G/T]CATTTTCGGATTTAG | 84669 |
rs182933881 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60247684 | TTGTTTTGGTTTTTT[G/T]TTTGTTTGTTTGTTT | 84669 |
rs182955566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410302 | CAGCTTTGACCCCCT[A/G]TGATTTCATCCCTGA | 84669 |
rs182975079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60365794 | AAATACCAAAAATAA[C/T]GCCCAGAACAAATAT | 84669 |
rs182981378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378247 | AAAATGACAATACTA[C/T]GTCACACCCATTAGG | 84669 |
rs182982971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60386971 | TTCTCCTTTACAAAT[A/G]GTAAGATCTGGTATA | 84669 |
rs182986780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416566 | GAGTCATTTTATGCC[A/G]ACCAATGGAATTTTG | 84669 |
rs183016005 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | USP32 | GRCh38.p7 | 17:60359900 | TGAGATGGAGTCTTG[C/T]TTTGTTGCCCAGGCT | 84669 |
rs183040248 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60400915 | GTGATCCCAGCTCTT[G/T]GGGATGCTGAGGCAG | 84669 |
rs183043282 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60329583 | CAAAGTGCTAGGATA[A/C]AGGCATAAGCCACCA | 84669 |
rs183077846 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60199445 | ATTATCCTGGAAATG[A/G]CTGTTAAATAAACAT | 84669 |
rs183091584 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60180915 | TGAGACAGGGACTTG[C/T]TCTATCACCCAGGCT | 84669 |
rs183116057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60242076 | GGTCTAAAATAATCT[A/G]TTTGTGTATGGATAT | 84669 |
rs183117589 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60222639 | AGGAAAACAAACTCA[A/T]ATATCACCACCCAGT | 84669 |
rs183133071 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60182023 | TTTATGTCAGATTCA[G/T]TTGAAAAAAATCTAA | 84669 |
rs183160571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274019 | CCTAGAAATAACAGA[C/T]GATGTAATTAACAGG | 84669 |
rs183174510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60310152 | AGGAATGTAAACTAG[C/T]ACAGCCATTGTGTAA | 84669 |
rs183175946 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60289254 | ACCTTGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 84669 |
rs183185480 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60329291 | GTGTTTTTTTTTTCA[C/G/T]GTAAGAATTGTCCTA | 84669 |
rs183186759 | snp | A/G | 0.000339807 | 0.0130303 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294804 | AGACTAAAAATGTCT[A/G]AGAAAAAGAAAGATA | 84669 |
rs183198302 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60348455 | GGAAAAGGGGACTTA[C/T]CAAGTTAAGGCAGAA | 84669 |
rs183199304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60324054 | GGAAGGCCAAGGTAA[C/G]AAGATTGCTTGAGGC | 84669 |
rs183207604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390082 | GATTTTGCTATCTCT[G/T]CAAATACATGTGTTT | 84669 |
rs183212496 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60371831 | AGGAGACTTAGGCAA[A/G]TGACAGTGTTCAGGG | 84669 |
rs183238007 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60353821 | CAGAACTCACTGTCC[A/G]TGAAAGGAAAATAAA | 84669 |
rs183244702 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60202841 | AGGATGTTTGTAGAT[A/G]TAATTAAGTTGAGGA | 84669 |
rs183252126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354502 | TAGGACAAGAAGAAA[C/T]TGTATAATGCAGCAA | 84669 |
rs183255112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60398101 | CAGGCAGGGTGCTTC[A/G]TGCCTGTAATCCAAG | 84669 |
rs183265159 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377351 | TAGCATTTCATTTTT[A/T]AAAGTGCCTACAAAA | 84669 |
rs183289015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60238184 | TGTGCTTGATGATCA[C/T]TGAACATCTGGAGAA | 84669 |
rs183293278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60310643 | GGCGGAGGTTGCAGT[A/G]AGCCAAGATCGACCC | 84669 |
rs183296422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60348795 | TAAAGACTAAAGAGT[A/G]CTTGGCACACAGTTA | 84669 |
rs183300062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60280419 | GTAAGTTAATTATTC[C/T]AAGTCTGTACTGAAT | 84669 |
rs183302435 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60382158 | ATGTATCTTTCCCCT[C/G]GAACTACCTGCCTTG | 84669 |
rs183305380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315645 | TTCACAGCAGCATTA[C/T]TGACAATAGAAGAAA | 84669 |
rs183313058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354211 | ATATTATAACTTTTT[A/T]TCAAAGGTAATATTT | 84669 |
rs183313566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423113 | GCTTTTGAAAGGTGA[A/G]GGGCAAATCCAGTTC | 84669 |
rs183398527 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60200116 | GGAGAATCACTTGAA[C/T]GCAGGAGGCATAGAG | 84669 |
rs183425927 | snp | C/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60229382 | TATGTGATCTCACTA[C/T]ATATGCAGCCAGAAT | 84669 |
rs183430582 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60203733 | CGGCGTGTGCCACCA[C/T]GCCTGGCTGATTGTT | 84669 |
rs183430771 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60187295 | ACTATCCAGGCTAAA[C/G]AGCTCATTTAAAAAG | 84669 |
rs183440168 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60290680 | CAAAGTGATAAATGA[C/G]TCTGCATGCTAATGA | 84669 |
rs183444562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60332836 | TTATTCAGCATAATG[C/T]TTCTGAGATTCATTC | 84669 |
rs183446381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249580 | GGCATTTATTCCTGC[C/T]CTCCTTCAAATCATG | 84669 |
rs183448280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298718 | AAGAAATGCTAATTT[C/G]CAAAAATCAGGATCA | 84669 |
rs183452001 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60267645 | CCTGCCTCAGCCTCC[C/G]GAGTAGCTGGGACTA | 84669 |
rs183452185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60314926 | CAGAAGAAACAATTT[C/T]ACTATACTGAAAGAA | 84669 |
rs183489065 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60259143 | AAGCTTTCCTTTAGC[C/T]CCCTTTACACATTTT | 84669 |
rs183527257 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60262440 | CAGGTGATCCGCCCA[C/T]TGTGGCCTCCCAAAG | 84669 |
rs183544400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60299157 | CCTATCCCCTCCAAA[A/C]ACAAAAACAAAACCA | 84669 |
rs183555470 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60333190 | CCAGAAAAGCTTTAC[C/T]AATAGCCTGACAATC | 84669 |
rs183557366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377953 | TGGGCATTAAAAGAT[C/T]CTATCAAGACCATGA | 84669 |
rs183623335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194409 | CTCTTCCTTACTCCT[A/G]TGCCACTTGTGCATG | 84669 |
rs183659223 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60186900 | TCCCTCTAATGTATG[A/G]GAAGGTGGGTGAAGC | 84669 |
rs183665846 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60254777 | TGATTCATCTTTCTG[A/G]TCATACTGCCTTACT | 84669 |
rs183670577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235578 | TGGCAATGAGTGTAT[A/G]TATCAGTTGGCTCTC | 84669 |
rs183671691 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60213083 | AAAGGCAGCTAACAA[C/T]GTTGCCACAAAACTT | 84669 |
rs183675349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296474 | GATTGTCAGTCATCC[G/T]AGAAGCAACAGAGAA | 84669 |
rs183686173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60311585 | CCCAACACTTTGGGA[A/G]GCCGAGGATGGTGGA | 84669 |
rs183687595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60277010 | GCAGCTAAATTACTA[C/G]GAAGAGGGAGTTTAA | 84669 |
rs183739641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60338991 | CTTGGCTGATTGCAA[C/T]CTCTGTCTCCTGGGT | 84669 |
rs183747116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60384878 | TTTGGGAGGTGGAGG[C/T]GGGTGGATCATTTAA | 84669 |
rs183750164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60361637 | GCCTCTTGTTCACTA[C/T]TGCTTAGTAGTTTCT | 84669 |
rs183754041 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403100 | CACTGCAACCTCCAC[C/T]TCCCGGGTTTAAATG | 84669 |
rs183758272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302541 | ATTCCCAACTTACAA[C/T]GGGTTTATCGGGCTG | 84669 |
rs183758840 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP32 | GRCh38.p7 | 17:60210730 | AATAGTGAAGTATTA[C/T]CAAAAAAGGTTTACT | 84669 |
rs183787971 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60234910 | CATTTGACAGACGCA[A/T]GCTAGAAAATAATAT | 84669 |
rs183794883 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406106 | AGGCTGCAGAGAGCC[A/G]TGATCATACCACTGT | 84669 |
rs183809883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358141 | CATAGTATTGTTTCT[A/G]CTACTTTTTTATTGC | 84669 |
rs183810120 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406930 | TTTGTTTCTGATCAT[A/G]ATGGAGTTAAAAGGG | 84669 |
rs183842969 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410444 | GAGGCTGAGGCGGGC[A/G]GATCACAAGGTCAGG | 84669 |
rs183863776 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60196777 | TTGCGTTGAGCCGAG[A/T]TTGCACCACTGCACT | 84669 |
rs183910143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325052 | TGATTTAGCTACAGG[A/T]GTTATGAAAACTAAG | 84669 |
rs183921406 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60364828 | GTTCACTAATGTTTG[A/T]GAAGAAACAAAAACC | 84669 |
rs183929427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405452 | TCAGACAGTCCACCC[A/G]CCTCAACCTCCCAAA | 84669 |
rs183976443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60283115 | AAGGCAGCATCTGAA[C/T]TGGGCTTTGATGACA | 84669 |
rs183976607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60253129 | ACAAAAATAGTGCCA[A/C]TCCAAGTCCTTAGTA | 84669 |
rs183979843 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP32 | GRCh38.p7 | 17:60334909 | CGTGATCCACCTGCC[C/T]CGGCCTCCCAAAGTG | 84669 |
rs183982513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387908 | AAATATTAATACTTT[A/G]CTGAAATATGATTTC | 84669 |
rs183985432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60366281 | CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGGGAT | 84669 |
rs183994187 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60285966 | ACACAGTGAAGCCCC[A/G]TCTCTAATAAAAATA | 84669 |
rs183996778 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60244066 | TTTGAGATGGAGTCT[A/T]GCTCTGTCACCCAGG | 84669 |
rs184023534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60338660 | GCTTGACTTCAGGAG[A/G]TCGAGGATGCAGTGA | 84669 |
rs184025714 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60214967 | TCTTTTTGTTTGTTT[A/G]TTTGTTTGTTTGTTT | 84669 |
rs184028008 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60304376 | TATTTTTTTTTTTTA[C/T]GGAAACAAAAACAGA | 84669 |
rs184028085 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60321644 | ACATTCTTGAAATGA[A/G]TGGAAACACAACAGT | 84669 |
rs184032066 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60361158 | ACAACAACAAAAACC[C/T]GGTATATATAAAGCT | 84669 |
rs184045311 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177123 | TGAAGCATCCCCTCT[C/G]TAAGTCAGAAAGAAA | 84669 |
rs184050712 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60257789 | CCACACAGGCCAGCT[C/T]TTTGGTGTTTTTTTT | 84669 |
rs184062438 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60341195 | GGTGTTCTCTGTTCC[G/T]GAATTTGAATGTTGG | 84669 |
rs184067223 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306404 | GCACTTTGGAAAGCC[A/G]AGGGGGGTGGATCAT | 84669 |
rs184084721 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60188994 | TTCCTATAAGCAGGA[C/T]GTCCTAAAGAGCTTT | 84669 |
rs184091261 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60217504 | TTCACCATGTTGACC[A/C]GGTTGGTCTCGAACT | 84669 |
rs184097453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60386171 | AAATGAGAGGACTTA[C/T]TGGAATGCAGAAAGA | 84669 |
rs184188271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196459 | AACTAAACTGCTTAT[C/T]TATTATTTGCAGTTT | 84669 |
rs184192869 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179051 | CTGAAAGTTCTCTAT[C/T]GGAGAGCTTGTATGA | 84669 |
rs184210116 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60279530 | TCACAAGTAATTTTA[C/T]AAATAAAATCTGAAG | 84669 |
rs184212413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237537 | TATTAAGTTTCAAAA[C/T]ATTCTGATACACCTC | 84669 |
rs184213569 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60268523 | GGTTACAGTGAGCTA[A/C]GATCACACCACTGCA | 84669 |
rs184214492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60240814 | TCAGCATTCTATTAT[A/C]TGCCTCAATTAAAAT | 84669 |
rs184216103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60219101 | ACTTTAATCTTCAAA[A/G]ATATGCCTTTTGCTC | 84669 |
rs184221561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197450 | TCTCTACCAAAAAAG[C/T]AAAATTAGCCAGGCA | 84669 |
rs184229232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60250366 | AGTTGTAAAATAAGC[C/T]AATAAATATAAATAT | 84669 |
rs184241732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60291559 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTAT | 84669 |
rs184245581 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60325684 | ATAACCCCAGCACTT[C/T]TGGAAGTTGAGGCTG | 84669 |
rs184246015 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306652 | CGAAAGAAAAAAAAA[A/G]TGTCTTTAGCTATTA | 84669 |
rs184247206 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60261294 | AATAACTTCTATTAA[A/T]TTTATTGTTTGAAAA | 84669 |
rs184312002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60210812 | AGAGTGTACCTTTGG[C/T]CTTTATCCTACCCAC | 84669 |
rs184313065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60193978 | CTTCTGAAAATTTCT[G/T]TTACCTTTTTGCTCT | 84669 |
rs184382023 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360008 | GAGTAGCTGGGACTA[C/T]AGGCGCCCACCACCA | 84669 |
rs184433821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60342560 | GAGGCAGTAGGCCTT[A/G]CTGAGCTGCAGTGGG | 84669 |
rs184444381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413682 | CATCCTGGCCAACAA[C/T]AGTGAAACCCTGTCT | 84669 |
rs184466650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60321852 | TAACACCTCAGTGGT[A/G]ACTATTTTAATCAGA | 84669 |
rs184468073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286757 | TGTCATTCAGAAGCA[C/G]AGACCCCCTCCCTCA | 84669 |
rs184475247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60349198 | TATATATTAATCTAA[A/T]AGACTACCTGTATAA | 84669 |
rs184477134 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392610 | AATGGGGTTCTGAGG[G/T]ATGCGGCATATGGCT | 84669 |
rs184564730 | snp | G/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177829 | TACTTAGTTACATTG[G/T]TAATTACTATCTATG | 84669 |
rs184569886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381478 | TATCTGTCCCTTGGA[C/T]TATTTGCCTCCTACT | 84669 |
rs184585536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418675 | TTACAAGAATAAAAA[C/T]AAACAACCCCATTAA | 84669 |
rs184588482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330750 | TGGGGTCTCGCTGTG[C/T]TGGCCAGGCTGGAGA | 84669 |
rs184598021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373390 | TGTGCAATTCGGTTA[C/T]ACCAAATTTACTAAT | 84669 |
rs184605152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60304597 | AGAAGAAATGTAAAG[C/T]GTCTTTATAGAATAT | 84669 |
rs184610848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225416 | AAGCCGTGATTATGC[C/T]ACTGTACTCCAGCCT | 84669 |
rs184622225 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412000 | TAATTTAATATTTAA[C/T]AATGCTTCTGTTTAG | 84669 |
rs184624994 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60201148 | CAGGTGTGAGCCACC[A/G]TGCCTAGCCTAATTC | 84669 |
rs184630769 | snp | C/G/T | 0.00189859 | 0.0307525 | intron-variant | USP32 | GRCh38.p7 | 17:60183503 | AGGGTTCTGAAGATA[C/G/T]AAAATTTACATGGAA | 84669 |
rs184653011 | snp | A/C/T | 0.00239401 | 0.0345304 | intron-variant | USP32 | GRCh38.p7 | 17:60243406 | CAATGTTGATAAGTG[A/C/T]GGCAAAAGCAAGTAT | 84669 |
rs184653162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60264148 | TTAATTTATAAAGTA[C/T]ATGTTTATTTTTGCT | 84669 |
rs184684069 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418489 | ACCAAAAGCAGTTTC[A/C]ACAAAAGCAAAAAGT | 84669 |
rs184684905 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60268959 | TTTAATAATGGAATG[G/T]ATTTATGCTTACAAA | 84669 |
rs184686934 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232132 | ATGAAGCTCTAAGAT[A/C/T]AAATTATCTGACATG | 84669 |
rs184698746 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306983 | TTTAGCCAGAGATGT[G/T]AAAGATCTATAAAAG | 84669 |
rs184703541 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60399903 | ATCAAATCCTCTTTA[C/G]AGACTTTGGCTCTTG | 84669 |
rs184727438 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393588 | TTGGACCCAAGGTGC[C/T]GGTTAGGTAATTTAG | 84669 |
rs184731129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60374822 | TTTCAGCTCTACTAT[C/T]ATCTTATGGGATCAC | 84669 |
rs184735859 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60343961 | ATCGCTTGAACCTGG[A/G]AGGCGAAACTTGCCA | 84669 |
rs184742377 | snp | C/T | 0 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412948 | GACTATTTAGAAACA[C/T]GCTCTAAAGTTCCGA | 84669 |
rs184791542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295450 | CAAGGTTTCAGTCAC[C/T]TGTGGTTAACAGAGG | 84669 |
rs184799037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60204895 | CCTCCTGCCTCAGCC[C/T]CCAGAGTAGTTGAGA | 84669 |
rs184817035 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60250712 | CCCACCTACTCAAGA[A/G]GCTGAAGTGGAAGGA | 84669 |
rs184852222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326213 | TGCATTTCCTACTGA[C/T]ACATAGATTCATCAT | 84669 |
rs184852523 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60292335 | GTAAGCCAACAACAA[A/G]TCCTTTACTCCTCAA | 84669 |
rs184858110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402938 | TCCTGACAACATTGT[G/T]GTTAGGTTCCAAAGG | 84669 |
rs184871343 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60297401 | ACCCTGTCTCAATCA[A/G]TCAATCAATAAACTA | 84669 |
rs184892101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60331132 | TAGAAAAGGAAATGA[C/T]AGTTCTGTCCAATAG | 84669 |
rs184901763 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60311854 | AAAAACGGTAGATAT[A/G]TGTAGGTCTCCAGAG | 84669 |
rs184906093 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60350890 | TGTACCCCAAAAGCT[A/T]TTGAATTTTTTTTTT | 84669 |
rs184917008 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60251302 | ATAATAATAAATAAC[C/T]GTTTTTAAAACTTGT | 84669 |
rs184933745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60205217 | TACTAAATCCTGGCT[A/C]TGATCACTTATATTA | 84669 |
rs184935555 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232584 | TACAGTCTCATTCTG[C/T]TGCCCAGGCTGGAGT | 84669 |
rs184945331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60307026 | ATACTGATGAAAGAA[A/T]TTGAAGAGGACACAC | 84669 |
rs184945581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316967 | TGTATGATTCCACTA[A/T]ATGAAATATTTAGAA | 84669 |
rs184950166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254285 | CTCTGTGACTTAGTG[A/T]TCACTTCTGGTAGCT | 84669 |
rs184951432 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60355756 | TGGGAGGATCACTAG[C/G]GCCTGGGAGGTCAAG | 84669 |
rs184951585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60270344 | AGAATACAGATAGTA[C/T]ATTCCCAGAATCTAA | 84669 |
rs184958217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60226286 | AATCTGACAACTATG[C/T]AGTCTTCAGAAACAA | 84669 |
rs184959318 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60292572 | GTCCATAATCAATAC[A/G]AGAAAAAATTCTAGG | 84669 |
rs184959446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60384388 | GTAAAATCCCACTTT[A/G]GCATAGTTTTGCTTT | 84669 |
rs184961113 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60333755 | AAAGGAAAGAAAATC[A/G]TAAAGAAGAGAAAAT | 84669 |
rs184972618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378409 | TTAAAGGGTTAAATA[C/T]AGAATTACCATATGA | 84669 |
rs184972974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60184411 | GGAGCTAGCTAACAA[C/T]CAATGTTATTAATTT | 84669 |
rs184980763 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60398460 | CTGGTGTTCTGGCCG[C/G]AGGGAAGCAAAGAGA | 84669 |
rs184983090 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418274 | ATTTTTGTATTTTTA[G/T]TAGAGACAGCATTTC | 84669 |
rs184983854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400387 | TGCATTAATCCAGGC[A/G]TGAGGGTTAGGCGGT | 84669 |
rs184990141 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, missense, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421435 | GCAGGGGAGGCCCGG[G/T]CCGACGGCGGTCCCA | 84669 |
rs185052948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281875 | AATCAAAATCTTTGC[C/T]GACAGAGCCAGTAAC | 84669 |
rs185066105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60201527 | TTTATATTCTCATCA[A/G]CATGGTATGAGAGTT | 84669 |
rs185069836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60275283 | GAAACATGGTGAAAC[A/G]CCATCTCTACTAAAA | 84669 |
rs185083854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235459 | GAATGATGAGATAGA[A/T]AATGTAAAAAGTATG | 84669 |
rs185113519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60230105 | AGGCGTGAGTCACTG[C/T]GCCCGACCACAAATT | 84669 |
rs185121679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60187837 | ATCTATAAATTACTT[A/G]TAGGCACCCTCTTCT | 84669 |
rs185181467 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60279185 | ACCTTTAGTACAAAC[G/T]GCTTTAAAGATTAAC | 84669 |
rs185182385 | snp | C/T | 7.02112e-05 | 0.00592458 | intron-variant | USP32 | GRCh38.p7 | 17:60185421 | CTTCTTTCTTTTATG[C/T]CAGATTCCTGCTCTC | 84669 |
rs185190438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60237468 | TATGAAATTATTTTA[A/G]ATCATACAATTCAAT | 84669 |
rs185191923 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60257358 | GGAGTCAGTATGAAA[C/T]ACACAGTGGGAATTA | 84669 |
rs185195483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60314734 | CCTACCAATCCAAAA[C/T]GCTCAAAGAAACTCA | 84669 |
rs185209873 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60298169 | TAAACATGGGACACA[A/T]ATAACAGTATGCATG | 84669 |
rs185210269 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60332490 | ACGACTCTACTAAAA[A/T]TAAAAAAATTAGCTG | 84669 |
rs185271446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317961 | CTGCACTCCAGCCTC[A/G]GCGACAGAGCCAGAC | 84669 |
rs185301351 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60357329 | ATGGTGATACACGCC[C/T]ATGGTTCCAGCTACA | 84669 |
rs185305569 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60399232 | AGCAAAGTAAAAGCT[C/G]CTGCTCTCATGGAAT | 84669 |
rs185394088 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60221055 | TCTTCTGCAACAGAA[A/C]TTTTTTTTTTTAGTA | 84669 |
rs185397288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60300643 | GAAACAAATAGACTA[C/T]TATGTCTATGTCATC | 84669 |
rs185406392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60334160 | AGCAACAAGAGGTGG[C/T]CATGCAATTACTATA | 84669 |
rs185415443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60380009 | TATTTATGTACATAT[A/G]TATGTAAAAATACTC | 84669 |
rs185428914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60282485 | CAGCGTCCAAGGTAG[C/T]TGGGACTACAGGCAC | 84669 |
rs185433022 | snp | A/C/T | 0.0244723 | 0.108003 | intron-variant | USP32 | GRCh38.p7 | 17:60234345 | GTCTCGATCTCCCGA[A/C/T]CTCGTGATCCGCCCG | 84669 |
rs185436782 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60240979 | TCTGGTAGCCCCAGA[C/T]GGTTTAGACAAACAC | 84669 |
rs185437051 | snp | A/C | 0.106633 | 0.204807 | intron-variant | USP32 | GRCh38.p7 | 17:60209616 | CATGTCCTATAATCC[A/C]ATCAGAGCCATTGTA | 84669 |
rs185440997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60192160 | GCTGGGTACAGTGGT[A/G]TGCACCTGTAGTCCC | 84669 |
rs185442981 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60261972 | ATGATCAAAAGCCCA[C/T]TTGCTATACTGACAC | 84669 |
rs185460853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194860 | CCAATCACTGCCCTG[A/C]AATCCTCACTTGCCT | 84669 |
rs185463733 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60301306 | CTGCACTACTTTATA[A/C]TCCCATCAGCAATGT | 84669 |
rs185469168 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60318249 | ATAAACTCAGCATAT[A/G]TAAAGATATAGAAGA | 84669 |
rs185477367 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60214246 | TGTGCTCGGCCACAC[A/C]ATTAGTTTATAATGT | 84669 |
rs185481307 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60236819 | TTGTCTTTTCTCAAC[G/T]ATTCATATAAATAAA | 84669 |
rs185485758 | snp | A/G | 0.000774459 | 0.0196629 | intron-variant | USP32 | GRCh38.p7 | 17:60236251 | ATCCTCTGTATGTAC[A/G]AAAGAAATTAAATAC | 84669 |
rs185490703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60385699 | ATACAAAAATGAGCC[A/G]GGCATGGTGGTGGGT | 84669 |
rs185492960 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60195442 | TACAGGGTTGAAGCA[A/G]TTCTCAGGCCTCAGC | 84669 |
rs185505563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403991 | GCCGCAGTGAGCCGC[A/G]ATCACACCACTGCAC | 84669 |
rs185522079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60304014 | TCTGAGGAGATAAGG[C/T]TGGGGATTTTCAAAA | 84669 |
rs185522276 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60338477 | AGCGCACATCTGTAA[C/T]CCCAGCAATTTGGGA | 84669 |
rs185526183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60278380 | AGTACAATGAAAAAA[C/T]AGAGAGTTTTCTGGG | 84669 |
rs185536489 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP32 | GRCh38.p7 | 17:60383106 | CAAAAATTAGCTGGG[C/T]GTGGTGGCTTGTGCC | 84669 |
rs185551315 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60389337 | ACCTGTGGTTGAGAG[C/T]TTGAGACCATCCTGG | 84669 |
rs185553329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409337 | TATGCAACAGAGCGA[A/G]ACTCCGTCTCAAAAA | 84669 |
rs185562522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60300285 | TCTGTCTTTGGGGAG[C/T]TCAAAGAAAAGAATG | 84669 |
rs185572485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60261036 | ATTTCAACTCATTCA[A/G]GAGTTTTACACTGAA | 84669 |
rs185614636 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60326359 | CTCGTCGCCCCGGCT[C/G]GAGTGGAATGGCGCA | 84669 |
rs185616301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60368037 | ATATAAGAAACATGA[A/G]CATCCTTGGATTTCA | 84669 |
rs185617049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60285651 | AATACAAAGATGAAT[A/G]GGATAAATTAATTCA | 84669 |
rs185628342 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60213807 | TACTATAGTTGTTCA[A/T]AAATATTTATAACTT | 84669 |
rs185638646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60321096 | GGAGATCCAGGGAAA[C/T]AGAAAGTAAAAAGAA | 84669 |
rs185645675 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408117 | AGAAAAAGAAAGAAA[A/C]AGAAAAACAATGTGA | 84669 |
rs185653319 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60255955 | ATATATACACATATT[A/G]TTCTCTAAAGAGAAA | 84669 |
rs185676381 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60360487 | AACATGGAGAAACCC[C/T]GTATCTACTAAAAAT | 84669 |
rs185684956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60402031 | CTAACTTATCCCAGA[A/T]CTTCTAGTTTTTGTC | 84669 |
rs185708386 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60281221 | AAGTGTTCACAAATA[C/T]AAGAGGATGCATATT | 84669 |
rs185712343 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178429 | CCCTTCCCTCAGCAT[A/G]GGTGGGGCCGGGGGT | 84669 |
rs185739980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60344868 | AGTGTCTCACTATGT[C/T]GCCTAGACTGGACTC | 84669 |
rs185745057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218268 | GGGCGCCTGTAGTCC[C/T]AGCTACTCAGGAGGC | 84669 |
rs185759017 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306069 | TAATGTCTAAGTACC[C/G]TTTTTTCACTCAAAA | 84669 |
rs185764276 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60266802 | TGGGACTATAGACAC[A/G]TGCCACCATGCCTGG | 84669 |
rs185781699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60323850 | CTGTTTTCTAAAAAG[C/T]GTCAAAACATCTCTA | 84669 |
rs185791834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363380 | GAATTGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 84669 |
rs185797984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60340092 | CCAAGCTCTCCATAG[A/G]ATTTTTTTTTCTCCA | 84669 |
rs185816909 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60202045 | TATTATCTTCCAAGG[C/G]CTGTTTCATTGTTTT | 84669 |
rs185851822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244681 | CTGTCGCCCAGGCTG[A/G]AGAGCAGGCGTTCCA | 84669 |
rs185859995 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60370992 | CAGCACTTTGAGAGG[C/T]CAAGGCTGGAAGATT | 84669 |
rs185873649 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60239923 | ATATTTTTTAGTAGA[A/G]ACGGGGTTTTACCAT | 84669 |
rs185883848 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60196848 | ACAAAATAAAAATAA[A/G]TAAATAACTTATTTA | 84669 |
rs185884366 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410307 | TTGACCCCCTATGAT[G/T]TCATCCCTGACCCAA | 84669 |
rs185969070 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265689 | AGGCAAGAACTACTG[C/T]GCCCGGCCTTGCTCA | 84669 |
rs185972926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196354 | AGCAAGTCCTGGGAA[A/T]AGCCCTCGTCTAGAA | 84669 |
rs185973967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60199536 | CATTTAATTCCCTAA[A/G]AAGTTTGGTATTTAT | 84669 |
rs185975216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227077 | CATATTTTTTTCTTT[C/T]ACCAAACATTGTATT | 84669 |
rs185995324 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60347755 | GACTGGGATTACAGG[C/T]TTGAGCCACCGCACA | 84669 |
rs185996198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60385449 | TACTTTGGAGTCTGA[A/G]GCAAGAGAATCGCTT | 84669 |
rs185997392 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60389830 | GACCATCCCGGCTAA[A/C]ACGGTGAAACCCCGT | 84669 |
rs186075382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60332970 | TCTATGTATAGTACA[C/T]AGAACTTACATTTTC | 84669 |
rs186083144 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60314969 | CTAGGATTATATATC[C/T]AACAACAAAATGACC | 84669 |
rs186086805 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353954 | ATTAACCTTTTCTGC[A/T]GTGACACAGAATGGA | 84669 |
rs186107278 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377786 | TCTATCTAGGGAAGT[A/C]TTTTGGGTTTTAGAG | 84669 |
rs186115032 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60352829 | CTAAGGCATAAAGTA[A/C]AAAGGGAGGTAAGAA | 84669 |
rs186117524 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60395960 | AACGTGACACCAACA[C/T]ATTAAGAGAATTGAT | 84669 |
rs186118927 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60394964 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTGAG | 84669 |
rs186119440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415755 | TTTCTTGGAGTCTTT[A/T]TACAATTCTAATTGG | 84669 |
rs186168806 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60308575 | AAAGAAAATACAATG[G/T]GGGAAAGAACAGTCT | 84669 |
rs186170882 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60346543 | TTAACAAACTAAAAT[G/T]TTTAGATACTTATTA | 84669 |
rs186191276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60292957 | CCTTTTTATTGTTCC[C/T]TGGACATACAAGTAC | 84669 |
rs186195295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60242498 | TCACTGCAACCTCCG[C/T]CTCCTGGGCTCAAGT | 84669 |
rs186197094 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60262583 | CTGTTCTACTTGAAT[C/G]TTTGGAGGTTTCTCC | 84669 |
rs186201884 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60307856 | AGAGACATACAATTG[C/G]CTGGACGTTGAGAGG | 84669 |
rs186212894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60222718 | ACGGGGTCTTGTTCC[A/G]TCACCCAGGCTGGAG | 84669 |
rs186218749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327862 | CCCGGCCAGGTATGT[A/G]GACACTCAGGGCGGT | 84669 |
rs186233365 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60283542 | AGATGCAAGAAATAT[A/G]TCTGAGTTAAGATGG | 84669 |
rs186235566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60346060 | GTTAAATAAAACTCT[A/G]TGACATTTAGTCATA | 84669 |
rs186238349 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60376140 | AGCCTCAAATTTCTG[A/G]ACTCAAGAAATCCTC | 84669 |
rs186243685 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60388491 | ATGCTGTGTTCCAAG[A/C]ATTTAAAACACGTTT | 84669 |
rs186248014 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60368545 | CGGGGGAAACGAGGG[G/T]AAAATATATTTAAAC | 84669 |
rs186254122 | snp | C/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408459 | CTTGGCTCACTGCAA[C/G]CTCTGCCTCCCGGGT | 84669 |
rs186259386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414221 | TACAAAAATTAGCTA[A/G]GCATGGTGGCATAAG | 84669 |
rs186297051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197937 | AGAGGACTGAGATTA[C/T]ACAAATTTCCTGGTG | 84669 |
rs186325842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60328576 | GGGATCCACTAAATG[A/G]CAAGGCTAAAAGAGC | 84669 |
rs186337726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369821 | TAACTCACTGCAGAC[C/T]TGAACTCCCTGGCTC | 84669 |
rs186346423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60272330 | TGTGATAGCAATAGC[A/G]AAGCCATGAAAGCAT | 84669 |
rs186347477 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60309641 | GATCTGAAATCTTCA[A/C]AAGAAGACATATAAA | 84669 |
rs186347644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60358782 | GGATGACGGTGCTTC[A/G]CAAGGTTTTGATATT | 84669 |
rs186350182 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60186931 | ATCAGGGTTATGAAT[A/G]CTATCATGAGACTTC | 84669 |
rs186355711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60335978 | AAAGACTCACTTGGA[C/T]AGGATCCCAACTGTT | 84669 |
rs186355913 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60381751 | CTCTCCTATTACTTA[C/T]GTAAACTGTACAAAT | 84669 |
rs186362604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60329234 | GTTAGTTGCTCCATC[G/T]TCTTGGTATATTTTA | 84669 |
rs186379996 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60297737 | TGAGCCATCACAACC[A/C]ACCTCAAAATATCAT | 84669 |
rs186380972 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60202511 | ATTGGGATTGTGCAT[G/T]AAGTCATCCGTAGAT | 84669 |
rs186383443 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60256702 | GTGAGGAAAGGAACA[C/T]CAATGCCTGCACCAC | 84669 |
rs186387278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185883 | CCTGGTCAAAAGAGT[A/G]AGACCCTGTCTCTGT | 84669 |
rs186387969 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60228633 | GACCAGCCCGAGCAA[A/C/T]GTGGATAGATCCCGT | 84669 |
rs186404482 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266276 | CTTGTAGGACTTCCT[A/G]CATATCATGAATCTG | 84669 |
rs186420086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228085 | GGCTGGAGGTCAGTG[A/G]TGCAGTCTCGGCTCA | 84669 |
rs186434694 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60288370 | GCTTGAGCCCAGGAA[G/T]TTGAGACTGCCGTAA | 84669 |
rs186444383 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60331694 | GTGGGAGGATTGCTT[A/G]AGTCCAGGAGTTCAA | 84669 |
rs186447429 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60375521 | ACCAAACACGTCATA[G/T]ATGCACACCCATGAA | 84669 |
rs186457779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60179702 | TTTGAGATGGAGTCT[C/T]GCTCTGTCACCAGGC | 84669 |
rs186525687 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60294106 | AGTCGGGGTCTTGCT[A/G]CATTGTCCAGGCTGG | 84669 |
rs186555989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60187203 | CTTCCCTATATGAGA[A/G]TCACGAGGCTCTCAA | 84669 |
rs186582934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60279069 | ACTTATTTCAAACTT[A/T]TAATTACATAGAATG | 84669 |
rs186587844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190860 | TATTAATAATTAGTA[C/T]AGTTTCAGGGAATCA | 84669 |
rs186596190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60246816 | TTTTTCATATATCTG[C/T]TGGCCATTTGTATGT | 84669 |
rs186606404 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60203341 | AGGAGGCGGAGGCTG[C/T]AGTGAGTGGAGATCA | 84669 |
rs186615588 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312428 | TGTTGTTGTTGTTGT[C/T]GTTGTCGTTGTTGTT | 84669 |
rs186621801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60351617 | ATTTTTAGTAGAGGC[A/G]GGGTTTCGCCATGCT | 84669 |
rs186633179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60251830 | AGAATGAACAGGAAT[C/G]CTAGCCAATCATTTA | 84669 |
rs186646910 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60207254 | AAACCAACGAGATGA[C/T]TGAATAATTTTTCAA | 84669 |
rs186723586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60382679 | TAACACTTTAAGCAA[A/G]TAACTTTCTAACTCT | 84669 |
rs186729502 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60360457 | TGAAGTCAGGAGTTC[A/G]AGACCAGCCTGGCAA | 84669 |
rs186734653 | snp | C/T | 0.0166424 | 0.0896896 | intron-variant | USP32 | GRCh38.p7 | 17:60401230 | GGGGGCCAAGGTGGG[C/T]GTGGTGGTGGGCGCC | 84669 |
rs186750744 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423961 | CTGCAGGCTGTACAC[A/G]AAGCATCTGCTTCTG | 84669 |
rs186753972 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60203663 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 84669 |
rs186802641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378257 | TACTATGTCACACCC[A/G]TTAGGATGGTTATTA | 84669 |
rs186828300 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP32 | GRCh38.p7 | 17:60191786 | AGTGCTGGGATTACA[C/T]GCGTGAGCCACCACG | 84669 |
rs186850641 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60233736 | GTCAACTTACATTTC[C/G]CCCACCTTATTAATA | 84669 |
rs186898243 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411406 | AGTCCCAGCTACTCA[A/G]GAGGCTGAGGTGGGA | 84669 |
rs186916112 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60239733 | TTCATTTATTTATTT[A/C]TTTATTTATTAGTTT | 84669 |
rs186918039 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60319321 | ATTAAGAATATTCAG[A/G]TAATAAATACGAGTA | 84669 |
rs186921935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60260774 | ATACAGTATTATTCA[A/G]TTTTTAAATATAGAA | 84669 |
rs186942135 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60300196 | ATTCTGTGTAATATA[A/T]ACAGCTGCCATACTT | 84669 |
rs186953175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60359403 | TTTGGATAAAGACAG[A/C]ATTTTTTAAATGATC | 84669 |
rs186953813 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60280999 | AGCAGCAATTCAGTT[G/T]TCTGTTGAATAAATT | 84669 |
rs186959977 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60333570 | GTGCCACTGCACTCC[A/G]CCTGGGTGACAGACT | 84669 |
rs186964049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400647 | GTTAAATAGAGAGTT[A/G]GATATTTAACTCTGA | 84669 |
rs186966054 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60364282 | CTTCATACAATCACA[C/T]TGGGAATTAGGTTTC | 84669 |
rs186971858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316697 | AATACAAAAATGAGT[C/T]GGGTGTGGTGGTGGG | 84669 |
rs186980006 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60355065 | AAAAACATAAAACTA[C/T]GATACATTCTTATTA | 84669 |
rs186983144 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60339532 | AGTTTGCAGTGAGCT[C/G]AGATCATGCTGTTGC | 84669 |
rs186983885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254426 | AAAACTTGGGCTGGG[C/T]GTGGTGGTTCACTCC | 84669 |
rs186987835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60303290 | AAACACCTTTATCCC[C/T]GGGGAAGGGCAGGAA | 84669 |
rs186996083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60263089 | TTGTAGCTGGAACTA[C/T]AGACATGTGCTACTG | 84669 |
rs187000665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235494 | TACCAATATTCTGAT[A/C]ATAAGCAGTGACAGA | 84669 |
rs187003480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60337827 | TCGAGGCTACAATGA[A/G]CCATGATCGGGCCAC | 84669 |
rs187008837 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60319810 | AATAATACAAAATTT[A/T]AAAATACACTATAAC | 84669 |
rs187009682 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60385307 | TCCCTTCGCTGACTT[C/T]CTTTTTGGACTCAGC | 84669 |
rs187016163 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60360163 | GTGAGCCACCGCGCC[C/G]GGCCCTGTAAGACAA | 84669 |
rs187039810 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60382218 | AGATGTCAAGTTCTC[A/T]CAGAGGCCTCCGCCA | 84669 |
rs187095307 | snp | C/G | 3.30262e-05 | 0.0040635 | intron-variant | USP32 | GRCh38.p7 | 17:60271346 | AAAATGGAATGATCC[C/G]TACCTTCACTTAGAG | 84669 |
rs187100777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302840 | AGAAATAAGTATTAT[A/T]GTAATCAGAAATAAA | 84669 |
rs187127248 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60337163 | CTAAACCTAGACTAT[C/G]TGGTAAATATGCAGG | 84669 |
rs187137219 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60212809 | CCCAGGTTGGAGTGC[A/G]GTGATGTGATCTTGA | 84669 |
rs187138029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381889 | TCCCAGTCGATACCG[A/G]CCCTCAGAGGTCACC | 84669 |
rs187142130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194099 | CCAGGCTGGAGTGCA[A/G]TGGCGCAATTATGGC | 84669 |
rs187162530 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422738 | GAAAGAAGAGAAGAA[A/C]AATGATAGGGTACCT | 84669 |
rs187165679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305304 | GAACAAGCATGTCAC[A/G]TGGTGAGAGAGGAAG | 84669 |
rs187170239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280253 | AGGCGTCCACCACCA[C/T]ACCCAGCTAACTTTT | 84669 |
rs187186625 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60221587 | TCTTGGCTCACTGCA[A/C]CCTCTGCCTCCTGGG | 84669 |
rs187193346 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60180697 | CTATGGCCAGGGTAT[A/G]GCACTAGGATCTGAG | 84669 |
rs187200818 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60322351 | GATATTGTTCTTAAA[C/T]CAATGAATTTAATAA | 84669 |
rs187202038 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60262258 | GTGCAATGGTGTCAT[C/T]TTGGCTCACTGCAAC | 84669 |
rs187203023 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60196756 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCGTTGAG | 84669 |
rs187204504 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177492 | ATTAAAAAAATTAAT[G/T]ACAACCAGTATAACA | 84669 |
rs187206798 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60298729 | ATTTGCAAAAATCAG[G/T]ATCACAATTATATTC | 84669 |
rs187208630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362728 | CTCGAATCAAATACA[C/T]AATTTATCATTCTCC | 84669 |
rs187218062 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403139 | GCCTCAGCCTCCTGA[A/G]TAGCTGGGTCTACAG | 84669 |
rs187232161 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60259363 | ATTGTAAACAATTCA[C/T]GTAACAATGCTGTGA | 84669 |
rs187238325 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60238656 | AAAAATACAAAAAAA[A/T]TAGCTGGTGTAGTGG | 84669 |
rs187239645 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP32 | GRCh38.p7 | 17:60215664 | ACTGCACCAGAAAAC[A/G]TATGTATATCTATTA | 84669 |
rs187276554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301988 | TCAGTAGAAACCATA[C/T]AGTACTCCATAAATT | 84669 |
rs187295864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60291772 | CAACTAGAGGTATCT[A/T]ATAGTTCAAATAGCC | 84669 |
rs187299167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326078 | CCCTGATAAAATTGA[A/G]CTAGGTAAGGATAGG | 84669 |
rs187303464 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306973 | TAGGAATCAGTTTAG[C/T]CAGAGATGTGAAAGA | 84669 |
rs187303521 | snp | C/T | 0.148744 | 0.228577 | intron-variant | USP32 | GRCh38.p7 | 17:60212146 | TATCTATCTAATTTA[C/T]ACCCATTCGATTGCT | 84669 |
rs187310074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60342765 | CTCCTCTGCTGGTTG[C/T]TAAGACCTTGGGGAA | 84669 |
rs187314985 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60387394 | ATCCTTTAACACTCA[A/G/T]TTATTGAGCATATAC | 84669 |
rs187319716 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60365810 | GCCCAGAACAAATAT[A/G]TAAGAGAAAAACCAG | 84669 |
rs187324017 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406440 | CTCCTCAGCCTCCTA[A/C]AGTGCTGGGATCACA | 84669 |
rs187370663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258220 | ATGAAATGATGCAAA[C/T]GATAAATGAACATTA | 84669 |
rs187372843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410529 | AAAAATTAGCTGGGC[A/G]TGGTGGCAGGCACCT | 84669 |
rs187406180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60198961 | TCTATAAAGAAATAA[A/G]TACAATTAGCTGGGC | 84669 |
rs187423734 | snp | C/T | 0.000269428 | 0.0116035 | intron-variant | USP32 | GRCh38.p7 | 17:60181789 | TCACAAATTCAAATG[C/T]CACAAAGTAAGCCAG | 84669 |
rs187436503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60241747 | TGTGTTGTAACAGTC[A/C]TTTATATATTCTGGA | 84669 |
rs187469096 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60283050 | AGTGTTGCAGAAATG[A/C]AAATAGTAAAATAAA | 84669 |
rs187473146 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60318446 | TGTGGTTAAGAAGCA[A/G]CAGGGAAAAGGACTT | 84669 |
rs187513379 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60329475 | ATTATAATTTGTTTT[C/T]ATTTATTTTTTTTTT | 84669 |
rs187520216 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60310571 | GGGCGTGGTGGCACG[C/T]GCCTATAGTCCCAGC | 84669 |
rs187527395 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60348666 | ATAGCTACTCAGGAG[A/G]CTGAGATGGGAGGAT | 84669 |
rs187533649 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60390744 | AATTACCATTTTATA[A/T]CCTTAGCTACTAAAA | 84669 |
rs187534264 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60338282 | GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC | 84669 |
rs187535160 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60372377 | CAAACTTAGATGGTA[G/T]AGACTACTACACACC | 84669 |
rs187539937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267961 | GATTACAGATGCCTG[C/T]CACTGCACCCAGTTA | 84669 |
rs187547489 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60291264 | AGACCAAAAATTATA[C/T]AGTCAAATCTGATTT | 84669 |
rs187550384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249654 | TGAAAGCTGCTCCTG[A/G]TTAAATTACCACACA | 84669 |
rs187568064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412063 | ATCAGCTCTGATGAG[C/T]CTGTTAGAGCCAGCT | 84669 |
rs187571802 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306638 | GCAAGACTCCGTCTC[A/G]AAAGAAAAAAAAAAT | 84669 |
rs187597573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60398166 | GCCAAGGAGTTTGAG[A/G]CCAGCTTGGGCAACA | 84669 |
rs187688009 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177953 | CCTTCAAGTATATAT[C/T]AAAAAACTACACGAA | 84669 |
rs187705002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60289817 | TAATGACAGTCAAGA[C/T]TGGAGCAGCTCTAAT | 84669 |
rs187715160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218144 | AAGAATTCTTACCAA[A/T]CAGGCCGAGGTGGAT | 84669 |
rs187717918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60248539 | AAACTCTGTTCATTT[A/C]TTTGGTCTTCTTTCT | 84669 |
rs187727456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60324481 | ATCAATGGGTTCCTA[C/T]AGATAGAATTTTATA | 84669 |
rs187744550 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60203963 | CTAAAACATAGGTTG[C/T]TAAATTCCTAGTTCA | 84669 |
rs187746121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229577 | CTTCCTGCCCATAAA[A/G]ATGGAGCAAGACAGA | 84669 |
rs187756709 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60187424 | ATTAACTGTCATCAT[C/T]TTTTGAACTGGTCAC | 84669 |
rs187759683 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60356253 | AGATGGGGCTAACAA[A/G]AGGTTAACCAAAAAA | 84669 |
rs187772291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320995 | CCTCCTACAGCTTGG[C/G]TCCGGATACAGACGC | 84669 |
rs187772579 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60379131 | TATTGCAGTCAAAAT[A/C]ATAATTTAGTACAAT | 84669 |
rs187781222 | snp | A/G | 0.000220266 | 0.0104921 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183172 | GGCCTCACCTTTCGG[A/G]CTGCTGATGATGTTA | 84669 |
rs187787795 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60210443 | CAGCCTCCCAAGTAG[C/T]TGGGATTACAAGCAT | 84669 |
rs187791010 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418307 | CATCTTGGCCAGGCT[A/G]GTCTCAAACTCCTGA | 84669 |
rs187793053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60398732 | TATGTAATCCTAGCA[C/T]TTTGGGAGGCTGAGG | 84669 |
rs187810750 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60273584 | ATCCAGATGCTCAGA[C/T]ACGTAACATCCACAA | 84669 |
rs187822756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60275597 | TGACCTTGGCATCTA[A/G]TAACTTTCATTTATT | 84669 |
rs187826600 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60252802 | ACTCAGCCATGTGTG[A/G]GATCTTGGCAAATAA | 84669 |
rs187826983 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60310805 | CTTTGGGAGGCCAAG[A/G]CAAGAGGATCACTTG | 84669 |
rs187834978 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60348815 | GCACACAGTTAATCA[C/T]TTTGATAAATGCTTG | 84669 |
rs187842937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60294486 | GCCTTTACAGTAGAA[G/T]TGAAAATTTTCAGAT | 84669 |
rs187856252 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423236 | TCACTCTGTCACCTA[G/T]GCTGGACTGCAGTGG | 84669 |
rs187868295 | snp | C/T | 0.0570934 | 0.159019 | upstream-variant-2KB, intron-variant, synonymous-codon | USP32 | GRCh38.p7 | 17:60392373 | GAGGGGGACGCATCT[C/T]CGCACGTAACGCATC | 84669 |
rs187956618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60242916 | GTCAATTTATAGAAA[A/G]AAGCTGGGATTTGAT | 84669 |
rs187969930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229116 | GGTCTTGCTCAGTCG[C/T]CTATAGCTCACTATA | 84669 |
rs187973890 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60196808 | CCAGCCTGGGTGACA[C/G]AGCGAGACTCTGTGT | 84669 |
rs187974570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60200172 | GCACTCCAGCCTGGC[C/T]GACAACAGCAAGACT | 84669 |
rs188015904 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60267386 | TCCAGCCCAAGCAAC[A/G]GTGCGAGACTTCGTC | 84669 |
rs188030243 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306223 | GAAGACGGAGTGTGA[A/C]TAGGATAGCAAGGAT | 84669 |
rs188032246 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60341179 | TGAGGAGTATCTTTG[C/T]GGTGTTCTCTGTTCC | 84669 |
rs188064633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60268704 | AAATAGAGATTTGAA[C/T]TTTTAGTTGAAAAAT | 84669 |
rs188071719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60230706 | CTGAAACTGTCAGCA[C/T]AACTCAGGTTCCTTC | 84669 |
rs188077966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60299226 | GTATGACAATTATAC[C/T]TCAATAAAACTTTTC | 84669 |
rs188111072 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295539 | CACTGTTCTGAGTAA[C/T]GTGATAAAATCTCTT | 84669 |
rs188122288 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60385056 | GAAGCAACTGAAGAA[C/T]CACAAAAGAAGTGAA | 84669 |
rs188123857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60329828 | TGCCAACACATAGAA[C/T]ACCAACTCCTGCGAC | 84669 |
rs188129681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373067 | AGCTACTCTATAGGC[C/T]AAGGTGGGAGGATAG | 84669 |
rs188132487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401022 | AAAAGCTGGCATGGT[A/G]GCATGTGCCTATAGT | 84669 |
rs188141033 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403104 | GCAACCTCCACCTCC[C/T]GGGTTTAAATGATTC | 84669 |
rs188171322 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60335316 | ATATTAAGTATGTGT[C/G]TGTCTTTCTTCATCC | 84669 |
rs188178778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318309 | AGTGATGACCTTTTG[G/T]CTTGTTTAGGCTAAT | 84669 |
rs188183001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60358567 | TAACAGAGGGAGACT[C/G]TGTCTCAAAAAAACA | 84669 |
rs188188851 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407302 | CATAAGTAGAGCTAA[A/G]TTCCAGGAGACTGAG | 84669 |
rs188191019 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60297026 | AGACTGACAGACTCT[C/T]TGTGGCAGAAAAATC | 84669 |
rs188201667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60311739 | CTGAGGCAGAAGAAT[C/T]CCTTAAACCCAGGAG | 84669 |
rs188202890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381488 | TTGGACTATTTGCCT[C/T]CTACTCCTCCAATTC | 84669 |
rs188203382 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60227715 | ACTGTGCCCAGTGGA[C/T]ATAAGTTTTCTACTT | 84669 |
rs188205286 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60277198 | GCAGTATACCATATT[C/T]CCAACATTCTAAGTA | 84669 |
rs188210609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400110 | GCTGGGATTATAGGC[A/G]TGCGCCACCATGCCT | 84669 |
rs188217582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330915 | CCCTCCATTCCAGGC[A/G]AGTTTCCAAGTCAAT | 84669 |
rs188224870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60182397 | TATTCCATGTCATGT[C/T]ATCTCTCACACCATT | 84669 |
rs188232046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60349308 | CTGGTGGCTGGGCAC[A/G]ATAGTTCACACCTGT | 84669 |
rs188254162 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60222911 | GGTCTCAAACTCCTA[A/C]CCTCAGGTGATCTGC | 84669 |
rs188295803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378045 | GTAAATCATATATCT[A/G]ATGTGAGAATAATAT | 84669 |
rs188318030 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417005 | TCACTGCAACCTCCC[C/G]CTCTTGGGTTCAAGC | 84669 |
rs188330092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261994 | TACTGACACCTGAGT[A/G]ATAATTAACACACTG | 84669 |
rs188338286 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60282533 | TAATTTTTGTACTTT[C/T]AGTAGAGACAGGGTT | 84669 |
rs188353278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60315879 | GACCATGGTAAAGCA[C/T]CCACGAAGTAACTAG | 84669 |
rs188355650 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60280495 | AAAATATGATTAAAC[A/G]TGGCAGTGTGTTCAA | 84669 |
rs188356023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60250452 | TACTATAATAAATTA[A/G]ATTGTAATATTCTAA | 84669 |
rs188387846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360536 | TGGTGGCACATGCCT[A/G]TAGTCCCAGTTACTT | 84669 |
rs188397971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402597 | TAGTAATCAGAATCA[C/T]GTTCCAGCACAGTAT | 84669 |
rs188399812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60279098 | TGTTTATGCTCCCTA[C/T]ACAAGCTTTCTGACT | 84669 |
rs188411934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204982 | TTTTTTAGAAGAGAC[A/G]AGGTCTCACTATGTT | 84669 |
rs188413358 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60286311 | GAAATAGGGTCTTTG[A/C]GGATGTAATGAATTA | 84669 |
rs188415319 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60189064 | TTATAGAGCCAAATA[A/G]TTTGTCATCATTGAC | 84669 |
rs188418598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60321729 | ATACAGTAACAACAA[C/T]AAAAAAATTTTAAGC | 84669 |
rs188420811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60304462 | TTATGCCATTAGAGA[C/T]ACATGTACCTCCATA | 84669 |
rs188430291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60361594 | AGTGGCTCTACCAAT[C/T]TACATTCCCACAATT | 84669 |
rs188434323 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60338808 | TATTTTCCATTTACC[C/T]TGTTTTCTCAATCCC | 84669 |
rs188436750 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60384426 | GTCCAGTGTCTAGTA[C/T]CCCAACAAACATGTT | 84669 |
rs188443097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232268 | ACCTCTGCTTCTTGG[A/G]TTTAAGCGATTCTCC | 84669 |
rs188477034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210774 | GTTTGACAAATTAGT[A/G]AAATGAATGACATCC | 84669 |
rs188522280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60253594 | AACATGGTGAAACCT[C/T]GTCTCTACTAAAAAT | 84669 |
rs188544292 | snp | A/G | 0.001298 | 0.0254424 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294853 | AAAGACCAAATATAC[A/G]TTGGTGGAAGTAGGG | 84669 |
rs188575247 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60321341 | ACATTGGAACTACAA[C/T]CAACGTAAGACTGGT | 84669 |
rs188582098 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60354315 | AAGACAGCCAAGGCA[A/G]GACCATGCATTCTGA | 84669 |
rs188597723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179494 | TAAATCCTTGCCAGG[A/G]AAGGGAAGACCAACC | 84669 |
rs188598295 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60397389 | TGTTTAAGACACAGC[A/C/G]TCTCTCTCTATCACT | 84669 |
rs188616378 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60341695 | CACTTGATTGAATCC[A/G]CTATTGAAACTTGTG | 84669 |
rs188632065 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60197611 | CTCTGCTGTAAAGGG[A/G]AAAAAAGAAAAGAAA | 84669 |
rs188646240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403063 | TGTTGCCAGGCTGGA[C/G]TGCAGTGTCACGATC | 84669 |
rs188649027 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60386753 | ACCAGCAAGTGATGT[A/C]CCCTCATTTTGCTCA | 84669 |
rs188678327 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60383209 | CCAAGGTCGCACTCC[A/T]GCCTGGGAAGCGACA | 84669 |
rs188720776 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60326403 | GCAACCTCCGCCTCC[C/T]AGGTTCAAGCGATTC | 84669 |
rs188734316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196547 | TAACTTATTTTGGCC[A/G]GGCACGATGGCTCAT | 84669 |
rs188762586 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60237814 | GTATATACTACATCT[C/T]GTTTAACCATTCATC | 84669 |
rs188775828 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60193291 | TAAACTAAAATAATT[A/G]GATCTTTCCATGACA | 84669 |
rs188790898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274054 | GCTTTAAAATGTCTA[C/T]TGTAAGTATCTCAGG | 84669 |
rs188799204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60235006 | CCCAAATTTCTTTAG[C/T]GCACAAAAGGACTAT | 84669 |
rs188833971 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60224101 | AATACATGATCTTTA[C/T]AATACGAAAATATGC | 84669 |
rs188845160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281927 | CAAATAATTCCAATG[C/T]TCAATATAGCTGGTA | 84669 |
rs188849860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60338554 | GGGCAACATGGTGAA[A/G]CCCCATCCCTACAAA | 84669 |
rs188858445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60240885 | TTACAGAACTTCTGA[C/T]GAATAACCCTGCCTG | 84669 |
rs188864217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60303762 | ATATATTGTCAGAGA[C/T]GAAGGAAAAATATGC | 84669 |
rs188865387 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP32 | GRCh38.p7 | 17:60261594 | GAGGTTCCAGTGAGC[C/T]GAGATCATTCCACTG | 84669 |
rs188872844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263356 | CAGAGTATCATTAAA[C/T]AGTCAACAGATGAAT | 84669 |
rs188904050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325451 | AAAAAGAAAGAAAAC[C/T]ATATCATAGTACACT | 84669 |
rs188908134 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60365044 | AGTAAATTCCTTATG[C/T]CTTTTAGTTAAGAAA | 84669 |
rs188937634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405692 | ACCTGAGCCTGGGGA[A/G]GTGGAGGCTGCAGTG | 84669 |
rs189009090 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60215210 | CTCCTGGGCTCAAGC[A/G]ATCCACCTGCCTCGG | 84669 |
rs189024663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60328448 | TGGCTACAGAGAGGA[A/G]CTGCCCACTGCAGGT | 84669 |
rs189026112 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177255 | CCACAGTATTTAATT[C/T]GTTTGTATACTAGTT | 84669 |
rs189044868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60346110 | TAATTTAGAAAATAA[C/G]TATAATTTTTTTTTT | 84669 |
rs189051426 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60388724 | CTACCAGTAATACAT[A/C]TCCCTAACAGTGTTT | 84669 |
rs189055083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369708 | CAGCAAATTAGTGAA[A/G]TAGTTGATTAAATTC | 84669 |
rs189070795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225648 | TCTGTCAAATTAGAC[C/T]GCCTTAATAACTATC | 84669 |
rs189071890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409218 | CTGGGCATGGTGGCA[C/T]ATGCCTGTAATCCCC | 84669 |
rs189073948 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60331555 | TGGCCACCAGAGTAA[C/G]ACCCCATCTCAAAAA | 84669 |
rs189074804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201251 | ATTCATTTTCATTCC[C/T]GTATAATGTTCCATT | 84669 |
rs189078840 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60183758 | GGCTTAGCCTAAGCT[C/T]CCACCCTCCACAGAG | 84669 |
rs189084030 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265775 | TCCTATGGTTTCATT[A/C]TTATTTTACATAGTT | 84669 |
rs189089042 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60351018 | CCTAAGCCAACCCAA[A/G]AAAGTTAAAACCTAG | 84669 |
rs189091440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60285655 | CAAAGATGAATAGGA[C/T]AAATTAATTCAAAAA | 84669 |
rs189098808 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60305012 | TTGTCCAAAGTCATA[C/T]ATCAATGAAGCAGCA | 84669 |
rs189101079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243658 | AAGCCACTTAAAACG[C/G]TAAAAACATTTTTAG | 84669 |
rs189103557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264423 | CTCGAAAGGCTGAGG[C/T]AGGATTGCTTGAACC | 84669 |
rs189109960 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60375164 | ATTCCTGTTTGTCTT[C/T]GTTTATGAAGCTCCC | 84669 |
rs189112284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243348 | ATCTTGATGCCTTTT[A/G]TTTCCTTTTCTTGCC | 84669 |
rs189114986 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60373724 | CCACAGTGTTGGGTT[A/G]CAAGCGTGAGCCACC | 84669 |
rs189116716 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394027 | CCTGGCAAACCAGAT[C/G]AGCAGCGTGGCATTA | 84669 |
rs189118647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413135 | AAATAGTACAAAACA[C/T]TTTTGAAAACTATTT | 84669 |
rs189130968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339199 | TGCAGGCATGAGCCA[C/T]CGCGCCCAGCCTAGA | 84669 |
rs189196245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60366830 | TTTAAGCCCACTCTT[C/T]TTTTTCTTTTGAGAG | 84669 |
rs189303136 | snp | C/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178458 | GTGCAGAATACATTT[C/G]TGAGGATACTTGAAG | 84669 |
rs189305471 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60251615 | ATGTGTAGCATAATA[G/T]CAATGTCACAAAGCA | 84669 |
rs189313037 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233252 | AGGAGAATCGCTTGA[G/T]CCCAGGAGTTCGAGA | 84669 |
rs189314994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60205303 | AAAAAGTAAAAAAAT[A/G]AAATTTGTAAAATTA | 84669 |
rs189326131 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60221171 | GGCCAAGGCAGAAGG[A/G]CTGCTTGAGACCAGG | 84669 |
rs189327234 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60307195 | AACTCAACCTCCCAG[A/G]TTCAAGCAATTCTCC | 84669 |
rs189328210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60251024 | CTTGGCTCACTGCAG[C/G]CTTGACCTCCTGGGC | 84669 |
rs189336357 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60270885 | AGCACCTCGGAGATG[A/G]TCTAGTCCAATAGTT | 84669 |
rs189340694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60292590 | AAAAAATTCTAGGCC[A/G]ACTCTACCTTTGAAA | 84669 |
rs189342511 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60333799 | TGTACTGTTTTTATC[A/G]TAAGTTTATGTCATC | 84669 |
rs189349242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326635 | CTGGGACTTAATACT[C/T]ATAGCAGCAGCACAT | 84669 |
rs189361096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244912 | GCTGGGATTACAGGC[A/G]TGAGCCATGGCACCC | 84669 |
rs189362455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326247 | TCAAAGATTGCATTT[A/C]ATCACACCCTCTGCC | 84669 |
rs189366647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60345104 | TAATTTTATAGAATT[A/G]ACTATGTTTTACTAT | 84669 |
rs189369472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60292445 | TTCTTGATATCCAAC[C/T]CCCTAACCTGCTTCT | 84669 |
rs189380073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201528 | TTATATTCTCATCAG[A/C]ATGGTATGAGAGTTC | 84669 |
rs189395572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60322095 | CAAAATAGGCCCACT[C/G]TTTTATAAGATGTGT | 84669 |
rs189397474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60286963 | AACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCTT | 84669 |
rs189408740 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392681 | TAGGGACGTCTTTGA[C/G]TGGGAGGGCGTTGTG | 84669 |
rs189421977 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60244104 | GCAGTGACGCGATCT[C/T]GGCTCACTGCAAGCC | 84669 |
rs189450828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312954 | TTAACATTTAATGCA[A/G]GCTCTGTGGCTGGGC | 84669 |
rs189462205 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60344508 | AGGCTGGAGTGCAGT[A/G]GTGCAATCATAGCTC | 84669 |
rs189489156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60387918 | ACTTTACTGAAATAT[A/G]ATTTCTACTGAACGC | 84669 |
rs189515932 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419531 | AGGTCAGGAGATGGA[A/G]GCCATCCTGGCTAAC | 84669 |
rs189540043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60202282 | TTGTCTTTTCTTGTA[C/T]CAATATGACATTATT | 84669 |
rs189543760 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60235796 | CTTTTTCTTTCAGCA[C/T]CAGGTTCCCCACAGG | 84669 |
rs189545937 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60255030 | CAAGCACCCATCTTT[C/T]AGACGAGTAATGTAG | 84669 |
rs189554280 | snp | A/G | 6.59413e-05 | 0.00574163 | missense | USP32 | GRCh38.p7 | 17:60185576 | CACTGGTGAAAGCAC[A/G]GAGACAGCTGTCCAG | 84669 |
rs189634935 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306984 | TTAGCCAGAGATGTG[A/T]AAGATCTATAAAAGG | 84669 |
rs189643740 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60188073 | GCAGCCTTGATCTCT[C/T]GGGTTCAAGCAGCCC | 84669 |
rs189648278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60279507 | AAAAAAAAAACCTTA[C/T]CTATATTTCACAAGT | 84669 |
rs189661460 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60226620 | TCAATGTAGAAAATA[C/T]AGAAAACATGAAGAA | 84669 |
rs189662632 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60257620 | TCAGCCTCCTGACTA[C/T]AGGCACAGGTTACCA | 84669 |
rs189669595 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60185191 | CACCACGTTGTACCC[C/G]TTGTGGCAGTTCTCA | 84669 |
rs189672203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404629 | AGGCATCTTGAAGCT[A/G]TGTATGGTTTATAGG | 84669 |
rs189679828 | snp | A/G | 0.000232423 | 0.0107776 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265468 | CAGAGAGATCCATAT[A/G]TAATTCCTTTAAAAA | 84669 |
rs189682172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60298562 | TATTTTTTTTGCTGT[A/G]CTGTTACCTTAAGCT | 84669 |
rs189684635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332760 | ATAGATTAGTTTGCA[C/T]TTCCTGGAATTTTAT | 84669 |
rs189690037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60314834 | TGAAAGCACTGAGAG[A/G]GAAAAAGGTATAAAG | 84669 |
rs189698704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353189 | TCATAGAAGAAGAGA[A/C]ACCAAAGGGCTCAAG | 84669 |
rs189700816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60352112 | CAGACAAAACAGAAC[C/T]CTGACTTTATTCAAG | 84669 |
rs189706466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60376873 | CATATCAGTTATCAG[C/T]TGGATAAAAGTTTTC | 84669 |
rs189707004 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60297832 | TTGAGATAAGCAATA[C/T]TGAAAACAGTTGCAG | 84669 |
rs189716202 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60394758 | TTTATTTATTTATTT[A/T]TTTGAGACGGAGTCT | 84669 |
rs189726553 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60252702 | GGAAGGAAGAAAAAG[C/T]GAAAGGGGAAGACAT | 84669 |
rs189740215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332172 | CTGAGGCACGAGACT[C/T]GCTTGAACCTGGGAG | 84669 |
rs189879205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60303549 | AAAAAAAAAAGTAAC[A/C]CTAGAATGGAAATTG | 84669 |
rs189896658 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60234356 | CCGACCTCGTGATCC[A/G]CCCGCCTTGGCCTCC | 84669 |
rs189904076 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60320710 | GGATGTGCTGCACAC[A/C]GTTATATAAACCTAT | 84669 |
rs189904548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60210055 | ACAATTACATTTTCT[A/G]GTCTTGTTGCATCCT | 84669 |
rs189906970 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | USP32 | GRCh38.p7 | 17:60204368 | ATTGCCCAGGTTGGA[A/G]TGGAGTGGTTATTTA | 84669 |
rs189909789 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60192470 | GACGGAGTTTCGCTC[C/T]TGTTGCCCGGCTGGA | 84669 |
rs189919064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337940 | GTGAATGGGCCATTA[C/T]CTAATAAAATGTTGT | 84669 |
rs189927791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60300801 | TTCCAGAACATTTTC[A/G]CCAACCCAAAAGGAA | 84669 |
rs189929868 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60334196 | ATAATATATATTACA[A/G]TTAATTTTATGCAGT | 84669 |
rs189933235 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60382390 | TAGTCCCCACAATTC[A/G]GGAGACCTGAACCAC | 84669 |
rs189939673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401032 | ATGGTGGCATGTGCC[C/T]ATAGTCCCAGCTACT | 84669 |
rs189942256 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | USP32 | GRCh38.p7 | 17:60380764 | CTATTCATACCCACT[A/C]CTCATTTGCTATTTG | 84669 |
rs189943775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214263 | TTAGTTTATAATGTA[A/C]CATATAATCTTTGTA | 84669 |
rs189943866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236960 | GTATTCCACTGTATG[C/T]ATATATTACATTTTG | 84669 |
rs189945089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423490 | GAGCCACTGTGCCCA[A/G]TTTTGCTCTGTCACC | 84669 |
rs189947314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375626 | TGTTTGTTTTTGTGA[C/T]GGAGTCTCGCTCTGT | 84669 |
rs189958114 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60196084 | CCATCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 84669 |
rs189965714 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418512 | CAAAAAGTGACTAAT[C/G]GGATCTAATTAAACT | 84669 |
rs189973441 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413721 | AATACAAAAATCAGC[C/T]GGGCATGGCAGCGTG | 84669 |
rs189983271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256856 | ACATTAATCAACTTA[C/T]TATTCCTCACAGATT | 84669 |
rs190130725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306121 | GAACAACTATTTAAA[C/T]GGTCACCTTATAATA | 84669 |
rs190167989 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60318046 | TGTTATTGATCATGA[C/G]TGTTAAACATTTTTA | 84669 |
rs190170647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60297525 | GCAATCTCGGCTCAC[C/T]GCAACCTCCACCTCC | 84669 |
rs190181035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60255992 | GACTTGCAGAATCAC[C/T]GAAGTGTATAGATCA | 84669 |
rs190197423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60240118 | ATTGATTTTAAATGT[C/T]TGTCTACTAAGTCCA | 84669 |
rs190197829 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60357830 | CTGGAGTGCAATGGC[A/G]CAATCTCAACTCACT | 84669 |
rs190209909 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60197268 | AAAGAACTTTTTTTA[A/G]TTACCATAAAACAGA | 84669 |
rs190213685 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60281662 | TCATTATCCCTGTTT[C/T]ACAAAGGAGGAAAAA | 84669 |
rs190244175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317403 | TGCCTGTAGTACCAG[C/T]GACTCGGGAGGCTGA | 84669 |
rs190249107 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60312013 | TTATCATGGCTTTTA[C/G]AGTCAGAAAGGCCTG | 84669 |
rs190350559 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60323968 | AATCAGCAGTGCAAA[A/C]TATAAAATGATTTTT | 84669 |
rs190360740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60364103 | CAAGATCAAAGTACC[A/G]GCAGATTCAGTGTCT | 84669 |
rs190363040 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60340968 | TTCTGGGTTGAAAAT[G/T]CTTTTCTTTAAGAAT | 84669 |
rs190371777 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60385499 | GCAGTGAGCCAAGAT[G/T]GCGCCACTACACTCC | 84669 |
rs190383364 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403481 | TACAATTCAGATTCC[G/T]CCCATTTGTAAGATG | 84669 |
rs190389510 | snp | A/C | 1.65034e-05 | 0.00287253 | intron-variant | USP32 | GRCh38.p7 | 17:60236275 | TAAATACATCAAACA[A/C]AGTGTGAAATAGGTG | 84669 |
rs190407591 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60195105 | GAATCAGGTGAGAGC[G/T]ACCATGCCTGGCTAT | 84669 |
rs190433483 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60278731 | CAGTTGAACCTGGAA[C/T]AGCAGGCATTTCAGT | 84669 |
rs190438586 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60194416 | TTACTCCTATGCCAC[C/T]TGTGCATGATTTCTT | 84669 |
rs190443788 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60191210 | AGGTCGAGACCAGTC[A/T]GACCAACATGGTGAA | 84669 |
rs190452475 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60218732 | CCCCAGCCTCCCAAG[G/T]AGCTGAAATTACAGC | 84669 |
rs190469564 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60300569 | ATTAAAAAAATTAAA[A/C]CTTTTACAAATAACG | 84669 |
rs190474409 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60261159 | TGTTTATCTTTGAAG[A/T]AATAATTGTCAATGA | 84669 |
rs190493476 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60379958 | GCAGCTTTCAATCTA[C/G]TTGGGAGAGTAAATT | 84669 |
rs190527130 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60368240 | GAGATACTGAAGCAT[C/T]TCACACTGTACAACA | 84669 |
rs190541528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200006 | CGAGACCAGCCTGGC[A/C]AATATGGTGAAACCC | 84669 |
rs190546080 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60181847 | TCACAACTGTACACA[A/C]AAAGGTAAAGACAGG | 84669 |
rs190561982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377829 | TATTCTGGTTTTCTG[C/T]AGCTGTGGGGTCACT | 84669 |
rs190566078 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242796 | GTATCCTTAGGTAAA[C/T]TGTGAAATCAGGAAG | 84669 |
rs190570191 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60262647 | GTACCCAAGGCCCTT[C/G]AAGATACGTCTCCAA | 84669 |
rs190582599 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60396866 | TTATACTCCTGTCTC[A/G]CCCTTCTCTACTCCA | 84669 |
rs190585486 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60222806 | CCTGCCTCAGCCTCC[A/C/T]GAGTATCTGGGATTA | 84669 |
rs190589411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302914 | AAATTCACTCATTCA[A/G]CAGTTCTTTGTTGAG | 84669 |
rs190596828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414762 | CTATTGCCTTCTTGT[C/T]CATCAAGTTGCTCAT | 84669 |
rs190600545 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60307876 | ACGTTGAGAGGAACA[G/T]ATCAGCAGAAGAACG | 84669 |
rs190605042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60386121 | GTGCCAATAATTAAC[C/T]ACATACCTCTAACTT | 84669 |
rs190642172 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305333 | AGCATGAGAGAGAGG[A/C]GGAAGTACCAGGCTC | 84669 |
rs190654047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60266543 | GCCCAGGCTAGAGTG[C/T]AGTGGCATGATCTCA | 84669 |
rs190660525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288404 | ACGATGGTGCCACTG[A/C]ACTCCAGCCTGGGAC | 84669 |
rs190670781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60322463 | TAAATCTTCACAAAA[A/C]TTTATTTATACAAAA | 84669 |
rs190699925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196410 | CAAATTTAATCTTGT[A/C]CAACTTTCATCTTTA | 84669 |
rs190725066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237514 | CAAAATGCTGTGTGA[C/T]CACCTCTTATTAAGT | 84669 |
rs190732597 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60213118 | GGAAAAGATACACTT[A/T]AAAAGTTTTTAATGG | 84669 |
rs190752047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267468 | GTCCACTTCCATGTT[A/T]CCTTTCCAGTATAAC | 84669 |
rs190753243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408183 | CAAGAAGCAGGGGGG[A/G]AAAATCAGGTGACAG | 84669 |
rs190772483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306275 | TGATGTCATTTTTTG[A/T]AAAGCACTTAATAAA | 84669 |
rs190773357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60273623 | ATCCAAAGAAAACAT[G/T]AAAGTAGTAGAAAAA | 84669 |
rs190774364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60341187 | ATCTTTGTGGTGTTC[C/T]CTGTTCCTGAATTTG | 84669 |
rs190789279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60202546 | TTGTAGAGAACTGAT[A/G]TCTTAAAATATTGAG | 84669 |
rs190792668 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60294192 | ATTACAGGTGTGAGC[C/T]ACCTTGCCTGGCCCA | 84669 |
rs190793738 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60252859 | ACCTAACAAATTAAC[A/T]CTATCAATTTTAAAA | 84669 |
rs190812852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60246638 | TTTTCCATATTGACT[C/G]TACTAATTTACATTC | 84669 |
rs190818644 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60196638 | GAGACCAGCCTGGCC[A/G]ACATGGTGAAACCCT | 84669 |
rs190826661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60328860 | CACCTGGAGCTACCT[A/G]CTCTGTGGCAGCAGC | 84669 |
rs190826813 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177330 | ATACAGTTCATATTT[C/T]GGTACATCAACACTA | 84669 |
rs190833011 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60228379 | GTCAAAAAAGAAGTA[C/T]AAATTAGTCCTAAGT | 84669 |
rs190847074 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60364777 | ACATAATAAAGGCCA[A/C]CATAATTTATCCATA | 84669 |
rs190850240 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410251 | GCTCATCTGGTCTTG[C/T]AACCTCCACCCAGAA | 84669 |
rs190869304 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60199043 | ATTGCCTGAGTCTGG[C/T]AAGTTGAGGGTACAG | 84669 |
rs190871629 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60180742 | TCATGTAAATGATCA[A/G]TAGGTGAAAAAATAT | 84669 |
rs190933713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60214853 | AATGGGGACCATACT[A/G]TTTTAGGAAATAATA | 84669 |
rs190959033 | snp | A/C | 0.00358779 | 0.0422022 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60176893 | TAGCAGGCACAGTTC[A/C]CAATAGGGTTCGTTC | 84669 |
rs190990008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60290191 | TTGCCCACCACCATC[A/G]CCCACCAACTGAAGT | 84669 |
rs190991390 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60309973 | TGTTTGAACCTGGGA[A/G]GTGGAGGTTGCAGTG | 84669 |
rs191001706 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60381819 | CCAAGGAATTATCCT[G/T]CAAAATTAAGATACA | 84669 |
rs191001888 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60294591 | AGTAATCTGCACATA[A/T]ACATCTGTTTGTCAT | 84669 |
rs191003949 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60329262 | TTATTGTTTTTGCCT[C/G]ACAATGTGTGTGTGT | 84669 |
rs191006234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60324944 | GGAGGCAGAATTTGC[A/G]GTGAGCCGAGATCAT | 84669 |
rs191012174 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60400392 | TAATCCAGGCGTGAG[A/G]GTTAGGCGGTGAGAG | 84669 |
rs191015833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60371636 | ATAAAGGGTGTTCAA[C/T]ATCACTTAGTCAAGG | 84669 |
rs191020704 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60395074 | TAACAATGGTATTTG[A/T]GTATCTAAACATAGA | 84669 |
rs191024062 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60347982 | AAAAAATTAGCCAGG[C/T]CTGGTGGCGGGCACC | 84669 |
rs191030244 | snp | A/G/T | 0.00279242 | 0.0372774 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421538 | CACGAAGGAAGGTCC[A/G/T]GGAGAAGGAATTCCT | 84669 |
rs191033181 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60272976 | AAATTTGTTTTGTTT[G/T]GTTGTTGTTTGAGAC | 84669 |
rs191038425 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60247416 | AACTCCTGGCCTCAG[A/G]TGATCCAGCCGTCTC | 84669 |
rs191057733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289164 | AGGCACCCACCACCA[C/T]GCCCGGCTAATTTTT | 84669 |
rs191068091 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60346742 | ATGCTAGAGAAAACA[C/G]AGAATTCTTCCAGAT | 84669 |
rs191072186 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60309282 | AAGGAGCTCAAACAA[C/T]TTACTAGCAAAAAAA | 84669 |
rs191099566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60389567 | AAAAGCTTCATAAAC[C/T]TTTTTTGTAATCTTA | 84669 |
rs191183861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197968 | AATTCATACTCTCTA[A/C]TTTTGCAACACAGAA | 84669 |
rs191207588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60229280 | CCTGGAGGATCCAAA[C/T]AATCCTCCTGCCTTG | 84669 |
rs191223225 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | USP32 | GRCh38.p7 | 17:60203696 | ATTCTCCTGCCTCAG[C/G]CTCCTGAGTAGCTAG | 84669 |
rs191227236 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP32 | GRCh38.p7 | 17:60187258 | GGATTTGATCGTGCA[A/G]TTAAGGTTCTAGCAC | 84669 |
rs191229886 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60333592 | TGACAGACTGAGACT[C/G]CATCTCAAAAACAAA | 84669 |
rs191242421 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60355070 | CATAAAACTATGATA[C/T]ATTCTTATTATAGAA | 84669 |
rs191251255 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60186952 | ATGAGACTTCACACA[A/G]TATATATTTGTGTCC | 84669 |
rs191258562 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60398289 | TAGTCTCAGCTACTC[A/G]GGAACCTGAGGTGGG | 84669 |
rs191264587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60191824 | AATGCCTACTTTAGA[C/T]TCAGTTTGCTAAGTC | 84669 |
rs191279833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60228937 | CACCCAAAGTGGTGG[A/G]ATTACAGGTGTGAGC | 84669 |
rs191314060 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60266876 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT | 84669 |
rs191335690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60397442 | ATCATAACTCACTGT[A/G]ACCTCAAACCCTGGG | 84669 |
rs191389363 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60382132 | TGAGATAAGCTCACC[A/G]GCAAACTGCCATGTA | 84669 |
rs191395517 | snp | C/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423090 | TAGAATTCATACTTT[C/T]CTGAGAAGCTTTTGA | 84669 |
rs191407528 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60300197 | TTCTGTGTAATATAA[A/T]CAGCTGCCATACTTC | 84669 |
rs191437184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194370 | GTATTCTCATACGTT[A/C]CAGAACCTGGAGGTA | 84669 |
rs191463211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60254769 | CCTCCTTATGATTCA[C/T]CTTTCTGGTCATACT | 84669 |
rs191471518 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60212869 | ACTGATTCTCGTGCC[C/T]CAGCTTCCTGAGTAG | 84669 |
rs191473213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60235550 | ATGATTAGAATTTTC[A/G]TTAGTGATCATTTGG | 84669 |
rs191475313 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60284598 | AAGATGATTTTCAAA[C/T]AAAACGGAGCCATTT | 84669 |
rs191483843 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60233806 | CTTTTCTAATTAATA[C/T]GTATTTTCAGAAAGT | 84669 |
rs191489723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60276075 | TACTTTGGAATGGGA[C/T]CTAATTTTTAAAATA | 84669 |
rs191524847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271558 | ATCCTGATAATATAT[C/T]TTCCACAGATATATT | 84669 |
rs191559644 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60337435 | TCTCTTGGTTATTGT[A/T]TTGGTCATTCTTTTA | 84669 |
rs191562900 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378138 | AAAAATGGGCAAAGG[A/T]TTGAATAGACATGTC | 84669 |
rs191580348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259041 | ATTGCTTCATTTTTG[C/T]AATAACACTTAAATT | 84669 |
rs191587653 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417461 | ATTTTTAATTTTTTT[G/T]TTTTTTTTTGTGACA | 84669 |
rs191606560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403074 | TGGAGTGCAGTGTCA[C/T]GATCTCGGCTCACTG | 84669 |
rs191619265 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60363165 | TAAATTAAAAAAAAA[A/T]TTTTTGAGGCCAGGC | 84669 |
rs191626870 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60298839 | AACATATACAAATGT[A/G]TAACTAAGTATGCTA | 84669 |
rs191637408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400712 | AGGAGTCATTAGAGA[C/T]TGATGGTATTGAAAG | 84669 |
rs191642687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333175 | GTATAACTTTGGACT[A/C]CAGAAAAGCTTTACT | 84669 |
rs191664179 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177724 | TTTTCTGAAAAGGAT[C/T]TCAATTTAGGTAGCC | 84669 |
rs191677156 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60239416 | TTCAAATATTCTGCC[C/T]TTTCCTTCTCTCTCC | 84669 |
rs191681931 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60259465 | GCGCGCCCTTCAGTG[A/G]GATGGAGTCTTGTCC | 84669 |
rs191688970 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60217377 | TCGGCTCACTGCAAC[C/G]TCTGCCTCCTGGGTT | 84669 |
rs191743823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60252126 | TACTAAAGAAAACTG[C/G]CTACCTTTTATCTCA | 84669 |
rs191748392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60208599 | ACAAATTCAGGCTAT[G/T]TAAATAAAGTAAATT | 84669 |
rs191749747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186223 | TGACAAAAACAAAAA[G/T]AATTGCATTTATTTA | 84669 |
rs191765847 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60215458 | CAAAATGAAATAAAA[C/T]TCAGTGAAAAAAAAA | 84669 |
rs191766035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60293165 | TTTATTCTACTTTAT[C/T]TTCCCCTATAGCACT | 84669 |
rs191801294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60319396 | TAGCTCTTGCCACAA[C/T]AAAAATTTTAAAACA | 84669 |
rs191830648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326108 | GAACTCTTGTTTTCA[C/G]TAACTCTTTTTTTAT | 84669 |
rs191844406 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60210629 | TTGTATTCTACAGAT[A/T]GAACTATCTTAGTTA | 84669 |
rs191845487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60343232 | CCCACTGACAATATT[A/G]GACAGATCAACGAGA | 84669 |
rs191848140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60359760 | AGACTGCAGTGACCT[A/G]TGATTGAACCACTAT | 84669 |
rs191853018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60387834 | AACACAGTAATGCAT[C/T]GAAAATCTCATGTAA | 84669 |
rs191853818 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60241971 | AGATTTTCTACATTT[A/G]CTTTTCTAGAAGTGT | 84669 |
rs191855417 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60365849 | TACCAAAGAGTTTGG[A/C]CTTGAATACAAACTT | 84669 |
rs191861962 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60299830 | CTGGGAAGTACACCA[A/T]CAATTCGGTGTCTGG | 84669 |
rs191869465 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406797 | GGGATTACAGACATG[A/C]GCCACTGCGCCTGGC | 84669 |
rs191870457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60283086 | TCAAAGAGAAATGGA[C/T]AAGCATGACAGAAAA | 84669 |
rs191873954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318722 | AGAACCAAAACACAA[A/G]AATTTTACTGAATTA | 84669 |
rs191875114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280562 | ATGAAAAAGTAATTA[A/G]AGGCATCTGCATGTT | 84669 |
rs191881966 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60348723 | CAGTGGGCCATGATC[A/G]TGCCACTGCACTCTA | 84669 |
rs191895080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237982 | AATTCTTGCTGAGGA[A/G]CTGCCAAACTGTTTT | 84669 |
rs191895255 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60338555 | GGCAACATGGTGAAA[A/C]CCCATCCCTACAAAA | 84669 |
rs191899619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60304224 | TTATAGCTGGATTAT[C/T]ATCAAAAATTATGTA | 84669 |
rs191902463 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60321568 | ATCAGGTGAGACACA[C/T]TGGATATAGACAAAG | 84669 |
rs191903412 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60339644 | CTCACCTAAAATATT[A/C]TCTGCATTGGAATGT | 84669 |
rs191905005 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60372409 | AGGCTATATGGGATG[G/T]CCTATTACTCCTAGG | 84669 |
rs191911471 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60390913 | TACACACACTGAAAT[C/T]CCAGTCATGAAAAAT | 84669 |
rs191915428 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410600 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 84669 |
rs191916296 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60280285 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 84669 |
rs191921480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315101 | CTACAAGAACGGCTA[C/T]AATAAAATGAATGAG | 84669 |
rs191937744 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60385376 | CACAAAGTCTGTTTG[A/G]TGGTCTCTTCACATG | 84669 |
rs192059743 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60358894 | ATTGAGAATCTCTGG[C/G]TTAGGCCAAAAAGAT | 84669 |
rs192062732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201334 | TGTTTTCATTTTGGG[A/G]CTACTATAGATAATG | 84669 |
rs192073922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60389956 | CGGGAGGCGGGGCTT[A/G]CAGTGAGCCGAGATC | 84669 |
rs192074213 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264447 | TTGAACCCAGGAGGT[C/T]GAGGCTGCAGTGAGC | 84669 |
rs192080699 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60285713 | CAGAGGAATGAGAGA[G/T]AATTTCTGATAAGAA | 84669 |
rs192084181 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60243989 | TTATTCTTTTACTTT[C/T]AACCTATTTGTGCCT | 84669 |
rs192103793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229803 | AAAGTTGATGCATTA[A/C]AAATTACTTTTTTTT | 84669 |
rs192120469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268444 | CAGGCATGGTGGTAC[A/G]TGCCTGTAGTCCCAG | 84669 |
rs192128356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60218844 | AAGTAATCTGCCCAC[C/T]TCAGCCTCCCAAATT | 84669 |
rs192130140 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60291494 | TAAATCTAAGCACTA[C/G]GTCCTTATATTTTAG | 84669 |
rs192142891 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60250243 | TTCATGCAGTTATTC[C/T]AAGGACCAGATGAGA | 84669 |
rs192145850 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60262353 | CCCAACACCATGCCC[A/G]GCTAATTTTTGTATT | 84669 |
rs192149164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192594 | CACGCATCACCACGC[A/C]CCGCTAATTTTTGTA | 84669 |
rs192156618 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60221998 | CAAAAACATAAACCA[C/G]AAAAATCCACCAAAA | 84669 |
rs192161201 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60344625 | CTGCTAATTTTTTTG[A/G]TTGCTGTTTTTAAGT | 84669 |
rs192167302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306644 | CTCCGTCTCGAAAGA[A/G]AAAAAAAATGTCTTT | 84669 |
rs192167504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60325652 | CAGTAAAGGGCCAGG[C/T]GCGGTGGCTCACACC | 84669 |
rs192179691 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417914 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGGCTA | 84669 |
rs192182472 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60341732 | TCACGAAGTTCTCGC[A/G]CCATGGTTTTCAGCT | 84669 |
rs192185072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302437 | TAGGCATGAGCCACC[A/G]CGCCTGGCCTGAGCA | 84669 |
rs192189728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388021 | TGACCCAAGCTATAT[A/G]ATCCTAGAGAGAGGG | 84669 |
rs192225962 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60212874 | TTCTCGTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 84669 |
rs192247967 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60196812 | CCTGGGTGACAGAGC[A/G]AGACTCTGTGTCAAA | 84669 |
rs192268121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60239820 | ATCACTACAACCTCC[A/G]CCTCCCGGGTTCAAG | 84669 |
rs192338767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60223315 | ACAGTAATTAAATGA[A/G]CCATCAATGTTTTGC | 84669 |
rs192352472 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | USP32 | GRCh38.p7 | 17:60183326 | GTGAGTGGTTTATGC[C/T]GGCAGAGAGCCGGGT | 84669 |
rs192362826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263315 | CAAACTATCCAAGGG[A/T]AACATCTAGATCTCT | 84669 |
rs192382394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60224752 | CATGCCATTGCACTA[C/T]AGCCTGGGCAACAGA | 84669 |
rs192386312 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60201072 | CATGTTGCCCAGGCT[C/G]GTCTTAAACTCCTGG | 84669 |
rs192393702 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296143 | CAAATCAGGGACATA[C/T]GATACAATGTTAAGA | 84669 |
rs192401561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330026 | TTTCTTTGAAGTTCT[A/G]GGTTGTAACTCCCTT | 84669 |
rs192407347 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60373122 | CTCTTGAGCCCAGGA[A/G]CTCGAGGCTACAGTA | 84669 |
rs192410852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60336070 | AGTAATTATACATAA[A/G]GTATTTTCTGTAAGA | 84669 |
rs192442078 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60379317 | TGAAGGACTTAGTAA[A/G]TGTGAAAACTTTGAA | 84669 |
rs192458852 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410323 | TCATCCCTGACCCAA[A/C]CAATCAGCATACCCC | 84669 |
rs192460997 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60399071 | GAGGTATTAGTCCAG[A/T]TTGAAGGAGTGGGAA | 84669 |
rs192465900 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418353 | CCGCTTTGGCCTCCC[A/C]AAGTGCTGGGATTAC | 84669 |
rs192508209 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60182684 | GGGAGGATTGATTGA[A/C]CCCAGGAGGTAGAGG | 84669 |
rs192520707 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60342049 | TGTGGTTTTTATCTA[C/T]CTTTGGTCTTTGATG | 84669 |
rs192559370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60367021 | TTTAGTAGAGACGGG[A/G]TTTCACCGTGTTAGC | 84669 |
rs192582688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407873 | GAGGCCAAGGCAGGC[A/G]GATTGCCTGAGGTCA | 84669 |
rs192596754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204746 | AGTGCTGGGAGTATA[A/G]ATGTGAGCCACCGCA | 84669 |
rs192617491 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60297268 | GCTGGGCATTGTGGT[A/G]CGTGCCTCTAGTCCC | 84669 |
rs192624255 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60311808 | CCAGCCTGGGCAACA[A/T]GAGCGAAATTCCACC | 84669 |
rs192641899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411740 | TAAGTGGAATTATAT[A/G]TTTGTTCATTTGTGT | 84669 |
rs192644452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60331104 | AACCAAAATACAAAT[A/G]CCCTAACAAAGATAG | 84669 |
rs192661891 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178078 | ACTACTGTAAAATTT[A/T]AAAAAAAGACAAATA | 84669 |
rs192668696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60350758 | AGATATAAACTCACA[A/G]GGACAGAGGGATAAA | 84669 |
rs192674091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401767 | ATCTCTGCCTATGCA[G/T]GAACTTCAGCCTGGT | 84669 |
rs192676225 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424445 | TAATGATATTGAAAC[C/T]GTCCCTAGAAACTTT | 84669 |
rs192678203 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393052 | TGTTTTGCATCCATT[A/G]CCACGTCCCATTTCC | 84669 |
rs192684268 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60373833 | CCTTAAAACACATTG[C/T]ACAGTGTCCAAAAAT | 84669 |
rs192692145 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60218250 | TGAGCCAGGTGTGGT[A/G]GTGGGCGCCTGTAGT | 84669 |
rs192710388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261027 | ATCTGATAAATTTCA[A/G]CTCATTCAGGAGTTT | 84669 |
rs192719612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243086 | CTTTTGTTGAATTTG[C/T]TTCCAAGGGTTTGAT | 84669 |
rs192721939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200360 | TGAGGTCGGGAGTTC[A/G]AGACAGCCTGACCAA | 84669 |
rs192749150 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60311435 | AATAATATGATTAAC[C/T]CTGAAGAGAGGGAAA | 84669 |
rs192762527 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60316211 | GCATATATGGAGCAC[A/G]TGCTTAAGAATATGC | 84669 |
rs192764060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348884 | TAATGATAAAACAAT[A/G]AGAACCACTAGTTGA | 84669 |
rs192765549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60250489 | AAGTCACTATAGCCA[C/T]ATAAAAGCCTTTATG | 84669 |
rs192776047 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60292019 | TCCACAGGACCTACA[C/T]CAATGACCTACCTGC | 84669 |
rs192776850 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60354355 | TAGGATAGGAGTTTC[C/T]GTTTTAACAGTTTGG | 84669 |
rs192827974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384147 | CTAGATTTTTCAGTT[C/T]AGTACTTGTGTTGCA | 84669 |
rs192869075 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392416 | CGCCAATCGCAGCCG[C/T]GCGCCCCGCCCGGGC | 84669 |
rs192870501 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60193482 | GGCCCTGTGAATTTT[A/C]CAACTTTTAAAAAAA | 84669 |
rs192883993 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60275142 | CATTTTGAGCACTCA[A/G]TAAATAAGTTTAATG | 84669 |
rs192885671 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60235031 | GACTATGGTAGGCAA[C/G]AATAAACCAGGTTCA | 84669 |
rs192902066 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60310572 | GGCGTGGTGGCACGC[A/G]CCTATAGTCCCAGCT | 84669 |
rs192914272 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60187695 | AGACAGGAAAGAAGG[C/T]TGATAAAAAACATAT | 84669 |
rs192933857 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60300583 | ACCTTTTACAAATAA[A/C]GTATATAAAATGTTA | 84669 |
rs192935749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261261 | AGATAGGAAAATCAC[A/G]GTGAAATATGAAAAT | 84669 |
rs192940895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60365736 | AAAGAATGCATTAAG[A/C]TAAACCATTTTTATA | 84669 |
rs192966139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268795 | CAACAGTACTAAATA[C/T]GATAAAAATATTGAA | 84669 |
rs192970170 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231762 | AAAAGGAAGATACAC[A/G]TTATGTAATGTAATA | 84669 |
rs192975120 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306976 | GAATCAGTTTAGCCA[C/G]AGATGTGAAAGATCT | 84669 |
rs192976577 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60333394 | ACTTGAGGTCAGGAG[C/T]TTGAGACCAGCCTGG | 84669 |
rs193025339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360851 | TACATAAAGTAGGCC[A/G]GGCGCGGTGGCTCAC | 84669 |
rs193032943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402629 | CATTACTTTGCTTAC[A/G]TGAGTATACCTGTGC | 84669 |
rs193043535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243354 | ATGCCTTTTATTTCC[G/T]TTTCTTGCCTAATTT | 84669 |
rs193054423 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405867 | TTCTTTCAAAGGTTA[C/T]TATTTGGCTGGGTGC | 84669 |
rs193073333 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60210790 | AAATGAATGACATCC[C/T]GAATTTAGAGTGTAC | 84669 |
rs193087533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254229 | TAAAAATCAGAGCGA[A/G]GGAATTAGTTTAACT | 84669 |
rs193118259 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60184001 | TTTAAAAGGTCTACC[C/G/T]GTCAGCCGGGCGCAG | 84669 |
rs193126281 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60284997 | TTGAGAGCTGAGCTT[A/C]TCTCTCTCCCCTACT | 84669 |
rs193132035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60320998 | CCTACAGCTTGGCTC[C/T]GGATACAGACGCAGT | 84669 |
rs193140175 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | USP32 | GRCh38.p7 | 17:60360472 | GAGACCAGCCTGGCA[A/C]ACATGGAGAAACCCC | 84669 |
rs193146592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60329486 | TTTTTATTTATTTTT[C/T]TTTTTTGAGATGAGG | 84669 |
rs193153445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295312 | CAATGAAATACTACA[C/T]AGAAGTTAAAATATG | 84669 |
rs193156713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60204080 | TTTTCTTTTTTACCA[A/G]AGAGTCAACCTTTAA | 84669 |
rs193163133 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60240445 | GTGGGGAGAGGGAGA[A/G]AAGAAAAGAGAGAGG | 84669 |
rs193167249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60281714 | TATTTCCCACAGCAA[C/T]AGTAAGTGGCAGGGG | 84669 |
rs193174579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60317578 | CCAATACTTTGGGAG[A/G]CCAATGCAGGAAGAT | 84669 |
rs193177217 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60356484 | AACATTTGAACACAC[A/G]CCCGAGTAGTATAGA | 84669 |
rs193179129 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60386937 | CATATAAGCAGACTA[C/T]TTAAAAACTGCCCCA | 84669 |
rs193284147 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60264134 | TCAAGGATTTTTTTT[A/T]AATTTATAAAGTACA | 84669 |
rs193287783 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60303781 | GGAAAAATATGCTAA[C/T]GGAGTTTGAAGAATG | 84669 |
rs193289464 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60338464 | GGCCAGGCATGGTAG[C/T]GCACATCTGTAATCC | 84669 |
rs193291371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60383052 | AGAAATGAAGACCAT[C/G]CTGGCCAACATGCTG | 84669 |
rs193300067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412156 | TCAAGCTCACCACAC[C/T]GGTATTTTCCAAATT | 84669 |
rs199497937 | in-del | -/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60247192 | TTTTCTTTTCTTTTT[-/G]TTTTTGAGGCGGAGT | 84669 |
rs199500544 | in-del | -/A | 0.029116 | 0.117091 | intron-variant | USP32 | GRCh38.p7 | 17:60316545 | TGTTCCTGTAACTAC[-/A]AAAAAAAGGAATGGG | 84669 |
rs199503346 | in-del | -/TA | | | intron-variant | USP32 | GRCh38.p7 | 17:60349677 | ACACATATATATATA[-/TA]CACACATATATATAT | 84669 |
rs199517729 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60379988 | TAATACACATAAAAC[-/AT]GTGTTATTTATGTAC | 84669 |
rs199558407 | snp | C/G | 3.30502e-05 | 0.00406497 | intron-variant | USP32 | GRCh38.p7 | 17:60198489 | TCAGAAGACAGGCCT[C/G]TGATTCCTCCCTTTA | 84669 |
rs199585017 | in-del | -/T | 0.0766824 | 0.180169 | intron-variant | USP32 | GRCh38.p7 | 17:60216961 | ATGATTAATGATTGA[-/T]TTCACAACTAATTAG | 84669 |
rs199592987 | in-del | -/GTAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60262198 | TATGTATGTATGTAT[-/GTAT]TTATTTATTTGAGAC | 84669 |
rs199628321 | in-del | -/CTTT | 0.0722614 | 0.17581 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406812 | GCCACTGCGCCTGGC[-/CTTT]CTTTCTTTCTTTCTT | 84669 |
rs199631640 | snp | G/T | 3.3384e-05 | 0.00408545 | missense | USP32 | GRCh38.p7 | 17:60226222 | GCTCAATTACCACAG[G/T]GTTGGCATCCTAAAA | 84669 |
rs199642457 | snp | C/T | 0.00399272 | 0.0445019 | intron-variant | USP32 | GRCh38.p7 | 17:60209338 | AGAACATTTTGTCTA[C/T]TGCTTACATTAGAAA | 84669 |
rs199646467 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60180898 | ATTATTATTATTATT[-/A]TTGAGACAGGGACTT | 84669 |
rs199657049 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60360186 | AAGACAAAGATCCTT[-/A]AAACCTGGCCAGGCA | 84669 |
rs199668486 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178008 | TATTTATACTTTTGT[C/T]CCAGTCTTGATTAGA | 84669 |
rs199681661 | snp | C/G | 0.00199795 | 0.0315433 | synonymous-codon | USP32 | GRCh38.p7 | 17:60301666 | TAAATTATTGAAGTG[C/G]AGCCCTTTGGATGTT | 84669 |
rs199686163 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308832 | ACTCAGGAGGCTGAG[A/G]CAGGAGAATTGCTCT | 84669 |
rs199691539 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227848 | TTTAGTAGCCAAAAA[A/T]TTTTTTTAAATTTTA | 84669 |
rs199695331 | snp | A/T | | | missense | USP32 | GRCh38.p7 | 17:60223535 | TTGTCAGAAGTGTTA[A/T]GTTGTCGAGCAAAGC | 84669 |
rs199703267 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305179 | AAAGAAAAGAGGTTT[A/T]TTTGGCTCACGGTTC | 84669 |
rs199708599 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388518 | GTTTTTAAGAATACA[G/T]AAGCCACAAACTTAG | 84669 |
rs199740646 | in-del | -/A | 0.0298908 | 0.118541 | intron-variant | USP32 | GRCh38.p7 | 17:60351942 | AGGGGTTCACCTGGC[-/A]AAAAAAAAACGCAAA | 84669 |
rs199746265 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60230641 | CTTCTCATTGTCTTC[A/G]GCTTTCTTTTCTATT | 84669 |
rs199754722 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60241448 | ATTTTTTTTATAATT[-/G]TTTTAAATCAACATT | 84669 |
rs199764317 | snp | G/T | 0.000115834 | 0.00760943 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266102 | GCAAACTAATGAAAA[G/T]AAACTCTTATGGAGG | 84669 |
rs199765756 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60282360 | AAACATAGTATACTC[-/T]TTTTTTTTTATTGAG | 84669 |
rs199766140 | in-del | -/TG | | | intron-variant | USP32 | GRCh38.p7 | 17:60329267 | GTTTTTGCCTGACAA[-/TG]TGTGTGTGTGTTTTT | 84669 |
rs199769573 | snp | A/C | 0.000149488 | 0.00864417 | missense | USP32 | GRCh38.p7 | 17:60212054 | TTTTACTACTATTTG[A/C]TATAAAAGACATCTC | 84669 |
rs199779287 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306435 | TTGAGGTCAGGAGTT[C/T]GAGAGCTGCCTGGCC | 84669 |
rs199789832 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413876 | CAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 84669 |
rs199835526 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60183471 | GGAGAAGTAAAGGTA[G/T]AAAACATCTGCATTA | 84669 |
rs199852454 | in-del | -/TTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60246411 | GTGTATATATATATA[-/TTT]TATTTTTTTTTTTTC | 84669 |
rs199891376 | in-del | -/TTTGTTTATTTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60302110 | TATATAAATATTTTG[-/TTTGTTTATTTA]TTTATTTATTTATTT | 84669 |
rs199894903 | snp | C/T | 0.000576744 | 0.0169717 | missense, intron-variant | USP32 | GRCh38.p7 | 17:60288594 | AGGGTAACATACACA[C/T]CTCCAGATAGAAGCC | 84669 |
rs199945638 | snp | C/G | 1.6476e-05 | 0.00287014 | missense | USP32 | GRCh38.p7 | 17:60222427 | TCTAGGTAAGGCCAG[C/G]TTTGCTCCATACCAG | 84669 |
rs199976887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232857 | TGGCATGAAAGAAGA[A/C]ATTTAAATCCTCATA | 84669 |
rs199996618 | in-del | -/TATG | 0.0337553 | 0.125452 | intron-variant | USP32 | GRCh38.p7 | 17:60262179 | TTATTTATTTTGTTT[-/TATG]TATGTATGTATGTAT | 84669 |
rs200026711 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60216901 | ATACATTTTAGGATT[A/G]GTTGTAAGATTACAG | 84669 |
rs200037233 | snp | A/C | 1.64732e-05 | 0.0028699 | synonymous-codon | USP32 | GRCh38.p7 | 17:60236210 | GTGTCCTGCTTGCAG[A/C]CCATACCTGCTCTCT | 84669 |
rs200044629 | snp | A/G | 1.65252e-05 | 0.00287443 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60294736 | CATCCACCACGTGGA[A/G]CATTCTTTCCATTTC | 84669 |
rs200047889 | snp | A/T | 0.000115715 | 0.00760553 | missense | USP32 | GRCh38.p7 | 17:60198266 | TGAACTCACCAATCC[A/T]GGGCATGATTACTAG | 84669 |
rs200065411 | snp | C/G/T | 0.000115344 | 0.00759341 | intron-variant, synonymous-codon, missense | USP32 | GRCh38.p7 | 17:60219655 | GCTGAGGAAACATTC[C/G/T]CAGGCTCATCATACC | 84669 |
rs200071576 | in-del | -/GA | 0.0146672 | 0.084371 | intron-variant | USP32 | GRCh38.p7 | 17:60240465 | AAAGAGAGAGGGAGG[-/GA]GAGAGAGGAAGAGAA | 84669 |
rs200078597 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60309415 | CCAGCCTGGGCAACA[-/A]TGGCAGAAACCCCTG | 84669 |
rs200079824 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60209723 | CTTAATGTCAAATGA[-/C]CCCCCCCCAAAAAAA | 84669 |
rs200083885 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60370597 | AAACCCTGCCTCTAC[-/A]AAAAAAAAATACAAA | 84669 |
rs200085645 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60329480 | AATTTGTTTTTATTT[-/A]TTTTTTTTTTTTGAG | 84669 |
rs200100116 | snp | A/G | 0.309648 | 0.24278 | intron-variant | USP32 | GRCh38.p7 | 17:60401726 | TCTCTATAAAAAAAA[A/G]AAAAAAAAAAAAAGA | 84669 |
rs200117637 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295241 | AAGAGCAAAACTTCG[A/G]AAAAAAAAAAAGATA | 84669 |
rs200134145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315869 | CCTGCAAACTGACCA[C/T]GGTAAAGCACCCACG | 84669 |
rs200141950 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60266687 | TTGAGATGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 84669 |
rs200146465 | snp | A/G | 8.25702e-05 | 0.00642482 | intron-variant | USP32 | GRCh38.p7 | 17:60236089 | GGCTGGAAGTCTCAC[A/G]CAGCTGAAAATCCTG | 84669 |
rs200149970 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410789 | ACATAGGTTAGAAAT[A/G]GAAACTGTCGGCTGG | 84669 |
rs200175189 | in-del | -/CT | 0.0360663 | 0.129354 | intron-variant | USP32 | GRCh38.p7 | 17:60358565 | GGTAACAGAGGGAGA[-/CT]CTGTCTCAAAAAAAC | 84669 |
rs200207670 | in-del | -/TTTAT | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420070 | ATTTTATTTATTTTG[-/TTTAT]TTTATTTTATTTTAT | 84669 |
rs200213426 | snp | C/G | 0.00102126 | 0.0225741 | intron-variant | USP32 | GRCh38.p7 | 17:60212015 | TAAAAAATAATACTG[C/G]AGACTTACCCTTGTG | 84669 |
rs200247474 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60241444 | TATTATTTTTTTTAT[-/A]AATTTTTTAAATCAA | 84669 |
rs200247739 | snp | C/T | 8.2445e-05 | 0.00641995 | missense | USP32 | GRCh38.p7 | 17:60223520 | AAACACTGGTTGTTA[C/T]TGTCAGAAGTGTTAT | 84669 |
rs200252048 | snp | A/C/T | 0.00120375 | 0.0245043 | intron-variant | USP32 | GRCh38.p7 | 17:60223592 | TACAGAAAGCCTATA[A/C/T]AAAAAAAAGAGGATA | 84669 |
rs200295075 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60299411 | TCTTCCATCATCCCA[C/T]AGCGGAAAGCAGAAG | 84669 |
rs200300632 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60206604 | GCCTAATTAACCTAA[C/T]TGTAAGTAATATAAA | 84669 |
rs200310243 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60330525 | CTCTCTCTCCCCCCC[-/T]CCCTCCTTTCTCTCT | 84669 |
rs200349183 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227065 | AAAAAAAAAAATCAT[A/T]TTTTTTTCTTTCACC | 84669 |
rs200365482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302367 | GGCCAGGCTGGTCTC[A/G]AACTCCTGGCCTCAA | 84669 |
rs200398949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60195956 | AATGGTACCACCATT[A/C]ACAAACAATTGTTCA | 84669 |
rs200406695 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60255065 | TTTTTTTTTTTTTTA[A/T]TATATGGTTTTGCAG | 84669 |
rs200421738 | snp | A/G | | | missense | USP32 | GRCh38.p7 | 17:60198291 | TACTAGCTTCCTGAG[A/G]TGGGAGTGGGCTCGC | 84669 |
rs200478675 | snp | A/G/T | 1.65776e-05 | 0.00287898 | missense | USP32 | GRCh38.p7 | 17:60226212 | ACAGATGATGGCTCA[A/G/T]TTACCACAGGGTTGG | 84669 |
rs200488928 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60325761 | CAAAACCCTGTCTCT[-/A]ACAAAAAAATACAAA | 84669 |
rs200491057 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60341572 | TCTTTTCACATAGTC[C/T]CATATTTCTTGGCGG | 84669 |
rs200504332 | in-del | -/TTTATT | 0.121369 | 0.214369 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417782 | ATTTTTATGTATTTA[-/TTTATT]TTTATTTTTATTTTT | 84669 |
rs200516481 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60251285 | CACTTAAAAAAAAAA[-/T]AATAATAATAAATAA | 84669 |
rs200522790 | snp | G/T | 0.000214651 | 0.0103576 | intron-variant | USP32 | GRCh38.p7 | 17:60214781 | GTACATTTCCTATGG[G/T]TACAGTAATCACAGT | 84669 |
rs200529353 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60309318 | CAAAAACAAACCCAC[-/A]AAAAATTACATTTCT | 84669 |
rs200531154 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60347195 | GAAGCTTTTTTTTTT[C/T]TTTTTTTGAGACAGA | 84669 |
rs200546301 | snp | C/T | | | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402246 | CCATCCCTCATTTAT[C/T]TTTTTTTTTTTTTTT | 84669 |
rs200584009 | snp | A/G | 8.55469e-05 | 0.00653958 | intron-variant | USP32 | GRCh38.p7 | 17:60226242 | GCATCCTAAAATCAG[A/G]AAATCAGAGAATAAG | 84669 |
rs200587474 | snp | C/T | 0.00019501 | 0.00987252 | intron-variant | USP32 | GRCh38.p7 | 17:60226267 | AATAAGAAGCAAAGT[C/T]TATAATCTGACAACT | 84669 |
rs200646774 | in-del | -/C | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232174 | TTCTTTTTCTTTTTT[-/C]TTTTTTTTTTTTTTT | 84669 |
rs200656569 | snp | A/T | 1.7789e-05 | 0.00298231 | intron-variant | USP32 | GRCh38.p7 | 17:60269583 | GGAAGAGATGCCATA[A/T]ATCACAGCCAAGCTT | 84669 |
rs200692170 | snp | C/G | 4.97806e-05 | 0.00498877 | missense | USP32 | GRCh38.p7 | 17:60207038 | GTCTGTGTTGGACTA[C/G]AAGCTGAAATTGGAG | 84669 |
rs200704637 | snp | A/G | 8.24165e-05 | 0.00641883 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181543 | CCCTCGACTCAAGGC[A/G]TCAGCCAGCTCACAT | 84669 |
rs200728476 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182467 | GTCTTAGTATTTTTA[C/T]GAAAATAGTTTTGGG | 84669 |
rs200738756 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60215334 | AGCAAAGGCCCAAGG[-/C]CCAAGGTCCAAATTA | 84669 |
rs200749752 | snp | A/C/G | 0.000103076 | 0.00717833 | intron-variant | USP32 | GRCh38.p7 | 17:60192977 | AAGCATTTCTGGTTC[A/C/G]AGGTCCAACTCCTCT | 84669 |
rs200771688 | snp | C/T | 3.46542e-05 | 0.00416244 | missense | USP32 | GRCh38.p7 | 17:60252393 | TACCTAATAATTTGT[C/T]CTTCTTCTTCCGGAG | 84669 |
rs200785728 | snp | C/T | 9.88321e-05 | 0.00702896 | missense | USP32 | GRCh38.p7 | 17:60236185 | ACTGCATGGAGATGA[C/T]AAACCAGTTGTGTCC | 84669 |
rs200789227 | in-del | -/C | 0.0225045 | 0.103662 | intron-variant | USP32 | GRCh38.p7 | 17:60389811 | ACAAGGTCAGGAGAT[-/C]CCAGACCATCCCGGC | 84669 |
rs200798078 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60349320 | CACGATAGTTCACAC[A/C]TGTAATGCCAGGACT | 84669 |
rs200846353 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182560 | TTGGGCACAGGAGTT[C/T]GAGCCCAGCCTGGGA | 84669 |
rs200863948 | snp | A/C/G | 0.476592 | 0.105621 | missense, intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422628 | AGGGGGTGAAGGGGA[A/C/G]AAGCCACTAGAGCAG | 84669 |
rs200874651 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227779 | GATTAAATAACTAAT[-/T]AATCACAAACAGTTA | 84669 |
rs200875222 | snp | A/G | 1.78388e-05 | 0.00298649 | intron-variant | USP32 | GRCh38.p7 | 17:60219793 | TCTTGATAACCTATT[A/G]TTTTAAAAGATAAAA | 84669 |
rs200889407 | in-del | -/C | 0.0799831 | 0.183287 | intron-variant | USP32 | GRCh38.p7 | 17:60340996 | AATGTTGAATATTGG[-/C]CCCCACTCTCTTCTG | 84669 |
rs200892726 | snp | C/T | 0.00199792 | 0.0315431 | missense, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179303 | CTCAAAGTCTTCATC[C/T]ATACTGCTTGTGTCT | 84669 |
rs200930573 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60340884 | TGACAAAATCTCTCA[C/G]CATTTGCTTGTCTGT | 84669 |
rs200943549 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60214439 | GGCTTTTAGCATAAT[A/T]ATTATAGGTAAAATC | 84669 |
rs200946094 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60200716 | CACAAAGGTAACTAT[A/T]ATTCTAAATGTTACA | 84669 |
rs200946847 | snp | C/T | 0.00177682 | 0.0297532 | synonymous-codon | USP32 | GRCh38.p7 | 17:60212025 | TACTGGAGACTTACC[C/T]TTGTGTCTATCTATT | 84669 |
rs200965508 | snp | A/G | 0.00150164 | 0.0273599 | intron-variant | USP32 | GRCh38.p7 | 17:60207165 | AGATGAGAAGGGGGA[A/G]ATGTTTCAGATAAAA | 84669 |
rs200970919 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60234742 | CTCAGAAAAAAAAAA[-/T]ATTTTTTTTTGTTTT | 84669 |
rs201017769 | snp | A/G | 1.65201e-05 | 0.00287398 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60294705 | AAACACTTCCTGAGT[A/G]TATCTGGGACTTTAC | 84669 |
rs201026362 | snp | A/G | 3.2963e-05 | 0.00405961 | missense | USP32 | GRCh38.p7 | 17:60226059 | CCAGCAGTTTCTGAG[A/G]CTTCAGATGCAGTAG | 84669 |
rs201029256 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | USP32 | GRCh38.p7 | 17:60222505 | TCCATGAATCAGCTG[C/T]GGAGTTCGTTTTAAT | 84669 |
rs201045699 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60254507 | GGAGTTTAATACCAG[C/T]CTGGGCAACATAGCA | 84669 |
rs201054197 | in-del | -/AATCA | 0.0528381 | 0.153711 | intron-variant | USP32 | GRCh38.p7 | 17:60213475 | TCATAAAAACATAAT[-/AATCA]AATAATAGTTGTTTT | 84669 |
rs201057872 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60246413 | TGTATATATATATAT[-/A]TTTTTTTTTTTTCTT | 84669 |
rs201070858 | in-del | -/C | 0.0166325 | 0.0896639 | intron-variant | USP32 | GRCh38.p7 | 17:60188474 | TTCCAGTATATGCAA[-/C]TTTATGTCTTGTTTT | 84669 |
rs201155437 | snp | C/G | 0.00199792 | 0.0315431 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271384 | AATAGGTGGTGAAAC[C/G]AATGGGCCAAATGTC | 84669 |
rs201161644 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60389614 | TGACATTTACTAAAT[-/G]GGACCATGCTTAAAG | 84669 |
rs201176428 | in-del | -/A | 0.0547245 | 0.156101 | intron-variant | USP32 | GRCh38.p7 | 17:60240497 | AGAGAAAAAAGGGAG[-/A]GAGAGAGAGAGAGAG | 84669 |
rs201201872 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60379747 | TTAACGTTCAGAAGA[C/T]GTATAAATGAGAGCA | 84669 |
rs201213363 | snp | A/G | | | synonymous-codon | USP32 | GRCh38.p7 | 17:60198289 | ATTACTAGCTTCCTG[A/G]GGTGGGAGTGGGCTC | 84669 |
rs201219280 | snp | A/G | 0.000889656 | 0.0210722 | intron-variant | USP32 | GRCh38.p7 | 17:60219831 | ACTAAAAAAAGAAAC[A/G]AAACTTGCCATTTTA | 84669 |
rs201223651 | in-del | -/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60314563 | GCTAGAACTGGGGGT[-/G]GGGGGAGGAAAGGAG | 84669 |
rs201234954 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418403 | GGCCTCTGTTTTTTT[-/TG]TTTTTTTTTTTTTAC | 84669 |
rs201269520 | in-del | -/AC | | | intron-variant | USP32 | GRCh38.p7 | 17:60202444 | CACACACACACACAC[-/AC]GCAGACTTTGCATTT | 84669 |
rs201283529 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60326979 | GAGGCGAGGAAAGGG[A/T]GGGGGAGGAAGTGAT | 84669 |
rs201290771 | snp | A/C | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420694 | AAACAAACAAACAAA[A/C]AAACCTCTTTCCTGA | 84669 |
rs201293326 | snp | A/C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60246108 | ACTGTGCTATTAAAC[A/C/G]CTAGAAGTCATTCAT | 84669 |
rs201301145 | in-del | -/AGCTACTCAGGAGCTGGG | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60359688 | GTGTGCACCTGTACC[-/AGCTACTCAGGAGCTGGG]AGCTACTCAGGTGGG | 84669 |
rs201302126 | snp | C/G | | | upstream-variant-2KB, intron-variant, missense | C17orf64, USP32 | GRCh38.p7 | 17:60422302 | AAGGGGCGCCAGCCT[C/G]TCCTGGCCTGCTGTG | 84669 |
rs201335097 | in-del | -/TTTTTTTCTTTTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60227264 | ACTAGTTTTCTTTTC[-/TTTTTTTCTTTTT]TTTTTTTTTTTGAGA | 84669 |
rs201336325 | snp | A/T | 3.40327e-05 | 0.00412495 | intron-variant | USP32 | GRCh38.p7 | 17:60288482 | GCCAATTATATATAT[A/T]AAAAAAGGCAAACAG | 84669 |
rs201347022 | snp | C/T | 0.000153929 | 0.00877159 | intron-variant | USP32 | GRCh38.p7 | 17:60391849 | CCCGTCGCGGGCCTC[C/T]CAGGCAGCTCGCCCA | 84669 |
rs201378109 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60357513 | CAACAGAGCAAGACC[A/C]TGTCTCTTAAAAAAT | 84669 |
rs201382281 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60206117 | TGAACCCAGGAGCTA[A/G]TGACCAGCCTAGGCA | 84669 |
rs201386903 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232474 | CATTGCACCTGGCCC[-/A]AATTTTTTTTTTTTT | 84669 |
rs201399712 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60368991 | ATTATTTTTTAAAAG[A/T]TTTTTTTTTTTTTTT | 84669 |
rs201407793 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60292779 | AGTGATCATGTGTGT[-/A]AAAAAAAAAAAAAAG | 84669 |
rs201411176 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60351452 | CTTCTTTTTTTTTTT[-/C]GAGATGGAGTCTCAC | 84669 |
rs201413343 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242116 | CCTGCACCGTTTTTT[G/T]TTTTTTAAAGAGACA | 84669 |
rs201430541 | snp | A/T | 0.000131998 | 0.0081229 | missense | USP32 | GRCh38.p7 | 17:60223555 | TCGAGCAAAGCAAAC[A/T]TCTGCCCCTGGTGTG | 84669 |
rs201446211 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60341094 | CTTTCTCTCTGGCTG[-/C]CCTTAACATTTTTTC | 84669 |
rs201454953 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60202451 | TATCAAATCACACAC[-/A]CACACACACACACAC | 84669 |
rs201455332 | in-del | -/TAA | 0.0592355 | 0.161582 | intron-variant | USP32 | GRCh38.p7 | 17:60279852 | AATAATAATAATAAT[-/TAA]TAATAATAATAATAA | 84669 |
rs201464834 | in-del | -/AAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60184810 | GTGAGACCCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 84669 |
rs201472643 | in-del | -/G | 0.077417 | 0.180873 | intron-variant | USP32 | GRCh38.p7 | 17:60179690 | TTTATTTATTTTTTT[-/G]AGATGGAGTCTCGCT | 84669 |
rs201475723 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60250790 | GACCCCATCTCAAAA[-/G]AAAAACCAAGACAGA | 84669 |
rs201508817 | in-del | -/C | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60239618 | CTCTAATAGATTTCT[-/C]ATTTCAGTTATTGTA | 84669 |
rs201521384 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60302139 | TATTTATTTATTTAT[G/T]TATTTATTTATTTGA | 84669 |
rs201549863 | snp | C/T | | | missense | USP32 | GRCh38.p7 | 17:60192913 | GTGAATGGATATTGA[C/T]AGCCCATACTGTCGT | 84669 |
rs201605753 | in-del | -/GCACCCC | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422032 | AGCACCCAGCACCCA[-/GCACCCC]GCACGGAGGGCTTAT | 84669 |
rs201613554 | snp | A/G | 3.29484e-05 | 0.00405871 | missense | USP32 | GRCh38.p7 | 17:60190636 | ATATAGGCATTTCCA[A/G]TGAAAGCTCTGTCTT | 84669 |
rs201662072 | in-del | -/TAAG | | | intron-variant | USP32 | GRCh38.p7 | 17:60326161 | GTCACTTTGATAAAA[-/TAAG]TAAATAAGTAAGATT | 84669 |
rs201686351 | snp | C/T | 0.000164734 | 0.00907413 | missense | USP32 | GRCh38.p7 | 17:60205629 | TAGTTAGGGTGAACA[C/T]TTCATTTGTAGATGG | 84669 |
rs201692157 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60241446 | ATTATTTTTTTTATA[A/T]TTTTTTAAATCAACA | 84669 |
rs201726260 | snp | A/G | 0.000132111 | 0.00812639 | intron-variant | USP32 | GRCh38.p7 | 17:60214805 | TCACAGTAAGAAAAA[A/G]GGCAGATGTGAAAAA | 84669 |
rs201753149 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60396069 | CTAAAGCACTTGAAG[C/T]TTTTTTTTTTTTTTT | 84669 |
rs201754306 | snp | A/G | 0.00127348 | 0.0252015 | intron-variant | USP32 | GRCh38.p7 | 17:60255283 | AGACACTCATGTTAG[A/G]AACATCTTTTTTTTC | 84669 |
rs201757343 | in-del | -/TT | | | intron-variant | USP32 | GRCh38.p7 | 17:60207890 | TCTGGTAGAAAACTC[-/TT]TTAAGTTTCTGGGTT | 84669 |
rs201757409 | snp | C/T | 1.84459e-05 | 0.00303688 | intron-variant | USP32 | GRCh38.p7 | 17:60212007 | AATCTCTTTAAAAAA[C/T]AATACTGGAGACTTA | 84669 |
rs201774601 | in-del | -/AG | 0.0839998 | 0.186933 | intron-variant | USP32 | GRCh38.p7 | 17:60220982 | ACAGAAACTCTGTAC[-/AG]AGTCTTTTAAGTCTC | 84669 |
rs201786399 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60304192 | AAACAAAATTACATT[-/A]AAAAAAAACCCAAAA | 84669 |
rs201805712 | snp | C/T | 0.000399281 | 0.0141238 | stop-gained | USP32 | GRCh38.p7 | 17:60236168 | TTTCCACTGTTGCCA[C/T]CACTGCATGGAGATG | 84669 |
rs201856017 | snp | A/T | 0.000216218 | 0.0103953 | intron-variant | USP32 | GRCh38.p7 | 17:60226002 | CCTATCCAGGGGGAA[A/T]AAACCAATAAACCTC | 84669 |
rs201896076 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178040 | AAAAAAATGAAGTAA[C/T]CAAAGAAACATAACT | 84669 |
rs201911130 | in-del | -/TTTTC | | | intron-variant | USP32 | GRCh38.p7 | 17:60284635 | ATTGAAAATTATTTG[-/TTTTC]ACTGATTAAATAAAT | 84669 |
rs201924371 | snp | A/G | 0.000296487 | 0.0121719 | missense | USP32 | GRCh38.p7 | 17:60222447 | CTCCATACCAGTGAT[A/G]AAGTGCTCTCCACAC | 84669 |
rs201933998 | snp | A/C | 0.00488054 | 0.0491574 | missense | USP32 | GRCh38.p7 | 17:60183298 | GGGCTCAGAGAGCTC[A/C]TCCCCCTGGGGTGTG | 84669 |
rs201935260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60226251 | AATCAGGAAATCAGA[A/G]AATAAGAAGCAAAGT | 84669 |
rs201964870 | snp | G/T | 0.478768 | 0.100824 | intron-variant | USP32 | GRCh38.p7 | 17:60206253 | GCCCATAAGGCAGAG[G/T]CTGCAGTGAGCCAAG | 84669 |
rs201967841 | snp | C/T | | | synonymous-codon | USP32 | GRCh38.p7 | 17:60198283 | GGCATGATTACTAGC[C/T]TCCTGAGGTGGGAGT | 84669 |
rs201996312 | in-del | -/G | 0.0372196 | 0.131242 | intron-variant | USP32 | GRCh38.p7 | 17:60329278 | ACAATGTGTGTGTGT[-/G]TTTTTTTTTTCATGT | 84669 |
rs202001884 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60205247 | AGCATATATAATACA[C/T]TGAAAATGCATTCAC | 84669 |
rs202004756 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60326826 | ATGTTCTGAGTTATA[-/T]TTATATAGATTACTA | 84669 |
rs202016511 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60297461 | TCTTTTTTTTTTTTT[C/T]TTTTTGAGACAGAGT | 84669 |
rs202019898 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60234743 | TCAGAAAAAAAAAAA[-/T]TTTTTTTTTGTTTTG | 84669 |
rs202049190 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418581 | TAAACAGACAACCTA[A/C]AAAATGGGAGAAAAA | 84669 |
rs202064971 | snp | C/T | 0.00199792 | 0.0315431 | missense | USP32 | GRCh38.p7 | 17:60183269 | ACTTTCTTCACCTCC[C/T]TTGCCAGAATCCTGG | 84669 |
rs202079564 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60398660 | GGAATACAAAGATGA[-/T]TTTTTTTTTAAGTTG | 84669 |
rs202088578 | in-del | -/AATT | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60371085 | AAAATAAAAATAATA[-/AATT]AATTAATTAAAAACA | 84669 |
rs202110833 | in-del | -/ACAC | 0.0704125 | 0.17392 | intron-variant | USP32 | GRCh38.p7 | 17:60388290 | ATTCAGCCGATTCTT[-/ACAC]ACACACACACACACA | 84669 |
rs202114126 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60362137 | CAAAGCATCAGGTTG[C/T]CCCATCTGCCACTAC | 84669 |
rs202119629 | snp | A/G | 0.000314114 | 0.0125283 | intron-variant | USP32 | GRCh38.p7 | 17:60255171 | TCATTTACCTTAAAC[A/G]TACCTGGAAAAGGAG | 84669 |
rs202121527 | snp | A/C/G | 0.000115314 | 0.00759241 | missense | USP32 | GRCh38.p7 | 17:60198332 | ACTTGAATCCAAACC[A/C/G]CATCATATAGGTCTT | 84669 |
rs202126341 | in-del | -/A | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419810 | CTGCAACTCAAGGTT[-/A]AAAAAAAATTATTAT | 84669 |
rs202148357 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60302117 | ATATTTTGTTTGTTT[A/G]TTTATTTATTTATTT | 84669 |
rs202153149 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245867 | AATGTGTTTTTTTTT[-/T]AAAAAGCTTTAAAAA | 84669 |
rs202153265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257234 | AAAAGCCTTATAGGG[G/T]GGATTCTGGGATTGG | 84669 |
rs202154853 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60269587 | GAGATGCCATAAATC[A/C]CAGCCAAGCTTCCTA | 84669 |
rs202179814 | in-del | -/A | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412535 | GTGATACCCTGTTTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs202188402 | in-del | -/CACAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60202445 | CAGCTTATCAAATCA[-/CACAC]CACACACACACACAC | 84669 |
rs202199889 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60341407 | TGCTTGTCTGTAAAG[G/T]ATTTTATTTCTCCTT | 84669 |
rs207476520 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60242206 | ATACTCACACTAAAG[A/C]CGTGAACTCCTGGGC | 84669 |
rs367543545 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60315356 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAC | 84669 |
rs367564793 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60209859 | AAACAGCGTTTGCTC[A/G]CATTGAAAGACATCC | 84669 |
rs367571500 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60369547 | TGTTTTTCAGATATA[C/T]GTAAGAGTAAAAATG | 84669 |
rs367576601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289047 | GAGTCTCACTTTGTC[A/G]CCCAGGCTGGAGTGC | 84669 |
rs367577366 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60182377 | CACTGTCAAAGTGAC[A/G]ATATTATTCCATGTC | 84669 |
rs367592546 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182307 | TCTATCAATATTTCC[C/T]GTATTAGAAATTAAA | 84669 |
rs367598033 | in-del | -/TC | 0.00476025 | 0.0485537 | intron-variant | USP32 | GRCh38.p7 | 17:60255305 | TTTTTTTCTTTTTTT[-/TC]TTTTTTTTTTGAGAC | 84669 |
rs367599069 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194655 | TTCTCTTTTCCAACA[A/T]TAAGTTCCTCCACCC | 84669 |
rs367601228 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60233935 | AGGTTTATTGTAACT[C/T]TAAGTTTGCCTTTAT | 84669 |
rs367612742 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60365822 | TATATAAGAGAAAAA[A/C]CAGAATAAATCTACC | 84669 |
rs367618781 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60193363 | TTCTTTAATCAGAAT[C/T]GCTGATGTGGTACAT | 84669 |
rs367648114 | snp | C/T | 3.59505e-05 | 0.00423957 | missense | USP32 | GRCh38.p7 | 17:60208111 | TGTTCTGAATTAAGT[C/T]CACAGAGATCACTCA | 84669 |
rs367660945 | snp | C/T | 9.91637e-05 | 0.00704074 | missense | USP32 | GRCh38.p7 | 17:60185617 | TCGGCTTGCGCTCGC[C/T]GACTCTGCTCCACAC | 84669 |
rs367661201 | snp | A/G | 0.000135704 | 0.0082361 | intron-variant | USP32 | GRCh38.p7 | 17:60252460 | AGGGAAAAAAATGGT[A/G]AATCAAAGTTTATTA | 84669 |
rs367704723 | snp | C/T | 8.27383e-05 | 0.00643135 | intron-variant | USP32 | GRCh38.p7 | 17:60222582 | GACAATGTTGACTTT[C/T]AATATTACAAAAGTT | 84669 |
rs367716124 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60340660 | AATTGGGGCATTTAG[C/T]CCATTTACATTTAAG | 84669 |
rs367720166 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60369337 | GACATCTGCCTGTAA[G/T]CCCAGCTACTTGGGA | 84669 |
rs367740272 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60347600 | CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 84669 |
rs367743880 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60323552 | GGTACACAACTCTAT[A/G]AACATAGTAAAAGCC | 84669 |
rs367749084 | snp | G/T | 6.74252e-05 | 0.00580586 | intron-variant | USP32 | GRCh38.p7 | 17:60192810 | ATCTAAAGCTGAAAT[G/T]CTACTAAAGTAATTC | 84669 |
rs367750657 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60358654 | ACTAGGAAAACAGAA[A/G]GTCAAGTAAGTTTTT | 84669 |
rs367765702 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60391723 | CGCTGCTTCCCACCC[C/G]ACCTCTCTCCTCCAC | 84669 |
rs367774619 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60334911 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 84669 |
rs367783613 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60267223 | CCAGCCTGGTCAACA[C/T]GGTGAAATCCCGTCG | 84669 |
rs367794928 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404664 | TTGTAGAAGAGTGCA[A/C]CTCAGCCTCCTTGGA | 84669 |
rs367808662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60189119 | CTGACAAAGATTTAT[A/G]AATCTATCAACTAGT | 84669 |
rs367858401 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60293013 | ATTCTCTTGATGAAA[A/C]GTGGTCCTCCAGATA | 84669 |
rs367883173 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60200766 | TCTTTACAGTTTTAT[-/AT]CCTATGCACAAGTAA | 84669 |
rs367932403 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60253175 | GAAAGGCAATACCAA[-/AA]GTCAAAATGCTATAC | 84669 |
rs367944832 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60272385 | CAGAATATACATCAA[A/G]AATCGCAAATAGGCT | 84669 |
rs367997887 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60202400 | AGTATCTTGGTTATT[C/T]CTGGTGCTTTGTATT | 84669 |
rs367998539 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60212241 | TACATTGCTTAACGA[C/T]GAGGTTATATTCTGA | 84669 |
rs368003725 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296023 | AGCATGAGAAAAAAA[G/T]CACCAAATTCATGAA | 84669 |
rs368015446 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60309723 | GGCAAATCAATACTA[C/T]AATGAGTTAAAATCT | 84669 |
rs368027361 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60273939 | CACTCCAGCCTGGGG[C/G]CAACAGAGCGAGACT | 84669 |
rs368051044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60266973 | TTTGTATTTTTAGTA[C/G]AGACGGGATTTCACC | 84669 |
rs368159562 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60385395 | TCTCTTCACATGGAC[G/T]CGCATGACAGTGTGG | 84669 |
rs368177387 | snp | C/G | 0.000115307 | 0.00759211 | missense | USP32 | GRCh38.p7 | 17:60236211 | TGTCCTGCTTGCAGA[C/G]CATACCTGCTCTCTC | 84669 |
rs368188847 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60344128 | AAGCCTAAAATTCCT[-/A]TTTTTTTTTTTTTTT | 84669 |
rs368192900 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60396032 | TGAGGATGTGGTCAC[A/G]TGTATTGTATTTTTA | 84669 |
rs368205060 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60324881 | GGTGGCGCATGCCTG[C/T]AATCCCAGCTACTCA | 84669 |
rs368210625 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60268030 | TGGCCAGGCTGATCT[C/T]GAACTCCTGACCTCA | 84669 |
rs368212137 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60364402 | TCTGTTTGTTTCAGA[C/T]AGAAGCTCACTCCAT | 84669 |
rs368212546 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60282255 | TCTGATATCATTTAG[C/G]TAACCAAAAGTTTTA | 84669 |
rs368223969 | snp | A/G | 3.29739e-05 | 0.00406028 | synonymous-codon, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265982 | ATAACTTACAGGAAT[A/G]TCATCAGTGCGGTTG | 84669 |
rs368231468 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60318015 | AAACAAACAAAAAAA[-/A]CAGCCAACTGGCTTT | 84669 |
rs368233296 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60271906 | AGCCTCAAATTCCTG[A/G]GCTCAAGCCATCTTC | 84669 |
rs368236407 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60201947 | TAGGCGTGAGCCACC[A/G]CACCCAGCCAAGTTA | 84669 |
rs368244048 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | USP32 | GRCh38.p7 | 17:60222469 | TCTCCACACAGGTTC[C/T]GGGACCATTTCATAG | 84669 |
rs368249293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60240265 | GAAATATTTCCCTCC[A/G]CCTCAGGGTTTGCTT | 84669 |
rs368262052 | in-del | -/TAATG | | | intron-variant | USP32 | GRCh38.p7 | 17:60283505 | AAGATAAGAAACTTA[-/TAATG]ATGGCACCAAGAAAG | 84669 |
rs368288136 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60321118 | TAAAAAGAATATTGA[A/G]GAGAGGAAGAAGCTC | 84669 |
rs368296284 | in-del | -/TTAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60344990 | TTAGAAACAGAATAT[-/TTAT]ATCAACTTAGCACAT | 84669 |
rs368297277 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | USP32 | GRCh38.p7 | 17:60351853 | CTATAATACCAAATA[C/G/T]GAAATATTAAACTGG | 84669 |
rs368369714 | snp | A/G | 1.65556e-05 | 0.00287707 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294757 | TTTCCATTTCTTCCC[A/G]TATAACATAGTTCCC | 84669 |
rs368383896 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60368915 | TTTCTGATGCAAGAC[A/G]ACATGGAGAAAATTA | 84669 |
rs368388553 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60229910 | CCTCTGCCTCCTGGG[C/T]TCAAGCAATTCTCCT | 84669 |
rs368389271 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60340468 | TGGTTTAAAGTCTGT[C/T]TTATCAGAGACTAGG | 84669 |
rs368391857 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60275183 | AAGTATTGGCCGGGC[A/G]CGGTGGCTCACGCCT | 84669 |
rs368396104 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366408 | GTGATCTACCTGCCT[C/T]GGCCTCCCAAAGTGC | 84669 |
rs368398194 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60251056 | CAAGCAATCCTCCCA[C/T]CTCAGCCTCCCAAGT | 84669 |
rs368410389 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60288457 | TTATAAGCATATTCT[C/G]ATATTACCAGCCAAT | 84669 |
rs368413503 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60246625 | CACCTCCATACTGTT[G/T]TCCATATTGACTGTA | 84669 |
rs368416983 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410843 | CTCAGCACTTTGGGA[A/G]GCTGAGGTGGGGGGA | 84669 |
rs368421162 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60315051 | AGTCATTAGGGAAAT[A/G]CAAATCAAAACCACA | 84669 |
rs368433375 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60358450 | TGTGGTGGCGGGTAC[C/T]TGTAGTCCCAGCTAC | 84669 |
rs368462508 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60206764 | GCTGTTGCCATGTTA[C/T]ATTAGATACAAGTTC | 84669 |
rs368469860 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410486 | ATCTTGGCTAACACG[A/G]TGAAACCCTGTCTCT | 84669 |
rs368478002 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60316346 | TACCTAAGTAAATGA[C/T]TGCAAGTGGGAAAAT | 84669 |
rs368505888 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60263440 | CAATCTAGTCACCAG[C/T]GAATATGGTTAATAG | 84669 |
rs368513005 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | USP32 | GRCh38.p7 | 17:60289260 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 84669 |
rs368519661 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60327993 | GCCTGCAGGTGCCCC[C/T]TGGCAGGAGCAGCCT | 84669 |
rs368573365 | snp | A/G | 0.000872688 | 0.0208706 | intron-variant | USP32 | GRCh38.p7 | 17:60211352 | AGTCACAGGTTAAGA[A/G]GCCAGTGACTCCAGA | 84669 |
rs368605093 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60240752 | TGTGCTTTTGGGTAC[G/T]TTAATTTCCCAAGGA | 84669 |
rs368607555 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60247684 | TGTTTTGGTTTTTTT[-/G]TTTGTTTGTTTGTTT | 84669 |
rs368619589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60397796 | TGATACTCAAAAAAA[A/G]TTCTGAGACAGAGAT | 84669 |
rs368626117 | snp | A/G | 4.52509e-05 | 0.00475641 | intron-variant | USP32 | GRCh38.p7 | 17:60209337 | CAGAACATTTTGTCT[A/G]TTGCTTACATTAGAA | 84669 |
rs368631615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60180446 | TCTAACAGAAATATC[C/T]ATTTCCTATTCAAGA | 84669 |
rs368636327 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60218175 | GGATCACGAGGTCAG[A/G]AGATAGAGACCATCC | 84669 |
rs368647836 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378120 | AAGCACACATCTCAA[C/T]TCAAAAATGGGCAAA | 84669 |
rs368652705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274242 | AGCTTGAAGGACAGG[A/C]AATAGAAACTATCTA | 84669 |
rs368695718 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60326765 | AATATTCCCCCCAAA[A/G]AGACTTACTAAGTTT | 84669 |
rs368709624 | snp | A/C | 0.00103903 | 0.0227692 | intron-variant | USP32 | GRCh38.p7 | 17:60192962 | CAAAAAGAGTGTAAG[A/C]AGCATTTCTGGTTCG | 84669 |
rs368720714 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242093 | TTGTGTATGGATATC[C/T]AAATTCTCCTGCACC | 84669 |
rs368761184 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60401177 | AAAAAAAAAAAAGAC[C/T]GGGCGCAATGGCTCA | 84669 |
rs368774578 | snp | A/G/T | 4.96309e-05 | 0.00498131 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265947 | ATTGGAAGTTTATAC[A/G/T]CAACAAGACATACAC | 84669 |
rs368798801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60398458 | CACTGGTGTTCTGGC[C/T]GGAGGGAAGCAAAGA | 84669 |
rs368808566 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60275778 | GTGCAGTGGTGTGAT[C/T]TTAGCTCACTGTAAC | 84669 |
rs368813905 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60237351 | AAGGTCTCACTATGT[C/T]ACCCAGGCTGGTCTT | 84669 |
rs368821824 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60328388 | GACCAGCTGAAGAGA[A/C]AAGCTACCCCTTCTG | 84669 |
rs368825356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305921 | CAAGTACAGCAATAA[C/T]CTAGAATCATCCAGT | 84669 |
rs368825449 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60317514 | AGTGAGACCCTGTCT[-/A]AAAAAAAAAAAAAAA | 84669 |
rs368829294 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60192952 | CAGAAGAGAACAAAA[-/A]GAGTGTAAGAAGCAT | 84669 |
rs368835253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60245179 | CAGAATGGTATATTT[A/G]TACTGTCTTTTATTA | 84669 |
rs368855174 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60226505 | TGGCAGCCATTTTTT[-/T]AACATTAAAAGTAAA | 84669 |
rs368857061 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60194218 | CTGGCTAATTTTTAC[A/C]TTTTTTGTAAAGACA | 84669 |
rs368872529 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60196560 | CCGGGCACGATGGCT[C/T]ATGCCTGTAATCCCA | 84669 |
rs368896615 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | USP32 | GRCh38.p7 | 17:60211528 | AACTGGAACAAACAA[C/T]ATGAGAACCAAAGCT | 84669 |
rs368918766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | CA4, USP32 | GRCh38.p7 | 17:60176782 | AGACAATTTTTCCAC[A/G]GACTGGGGGATGGGG | 84669 |
rs368942182 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408064 | GATGTCGCCACTGCA[C/T]TCCAGCCTGGGGTAC | 84669 |
rs368945307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60379909 | TTTGTGCTTAAAACA[A/G]TCCAATGTGGTTTTA | 84669 |
rs368966025 | in-del | -/AAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60359815 | GACCTTGTCTCTGAA[-/AAT]AATAGATAAATAAAG | 84669 |
rs368988764 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60300435 | CAGGGGAAATGGTGT[C/T]CTCTCATTATAGCAT | 84669 |
rs369003287 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60326459 | GGGATTACAGGCACC[A/G]ACAACCATGCTCGGC | 84669 |
rs369006282 | snp | A/G | 1.65603e-05 | 0.00287747 | intron-variant | USP32 | GRCh38.p7 | 17:60214826 | ATGTGAAAAAGAAGC[A/G]CCCCTCTCAGCAATG | 84669 |
rs369013598 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | USP32 | GRCh38.p7 | 17:60181422 | CAAGCTGACCATTGC[C/T]GTAGCCATTGCCACA | 84669 |
rs369025236 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60371252 | CTCTGTCTCTAAAAA[A/T]TAAAAAAAAAAAAAA | 84669 |
rs369036607 | snp | C/T | 0.000131991 | 0.0081227 | intron-variant | USP32 | GRCh38.p7 | 17:60345449 | GGAGGTGGATAACTA[C/T]CTCAAAGGAAAACTT | 84669 |
rs369045014 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60391799 | CCACGCCCTCAATCT[C/G]CCCTCTCCCTCCCGG | 84669 |
rs369051446 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60363775 | AAATGCTGAGATTAT[A/T]CACGTGAGCCACTGT | 84669 |
rs369054083 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60254719 | TAAAAATAATAATGA[C/T]AATAATAATAAAAGA | 84669 |
rs369060079 | in-del | -/CA | | | intron-variant | USP32 | GRCh38.p7 | 17:60300373 | ATATCCCACGAAACA[-/CA]GACGGACACTAAGCA | 84669 |
rs369064000 | snp | A/C | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420829 | TCTATGCATATATAA[A/C]TATATATGTACAAAA | 84669 |
rs369070465 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60202854 | ATGTAATTAAGTTGA[C/G]GATGTCAAGATGAGA | 84669 |
rs369082078 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393110 | ACTCTGTGCCTATTA[A/C]ACGGTAACTCCCCAA | 84669 |
rs369092558 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60349604 | AAAAAAAAATATATA[A/T]ATATATATATATATA | 84669 |
rs369094326 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60348203 | AACCTTGGAAAATGC[A/C]ATGGGGTTTTAGAAT | 84669 |
rs369099108 | in-del | -/CCAGCAC | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422036 | CCCAGCACCCAGCAC[-/CCAGCAC]GGAGGGCTTATTATT | 84669 |
rs369181948 | snp | A/G | 4.957e-05 | 0.00497821 | missense | USP32 | GRCh38.p7 | 17:60226201 | CTCCATTCAAAACAG[A/G]TGATGGCTCAATTAC | 84669 |
rs369210125 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60369736 | TTCAAGGTACTTATT[-/A]AGTTCTACACAATGA | 84669 |
rs369212443 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60191276 | GCATGGTGGCAGGCA[C/G]CTATAATCCCAGCTA | 84669 |
rs369250299 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60229117 | GTCTTGCTCAGTCGC[C/T]TATAGCTCACTATAC | 84669 |
rs369255540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286547 | ACCTTTTGAGGGGCC[A/G]AGGGGCCTAGGGGTC | 84669 |
rs369262528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60238636 | GGTGAAACCCCGTCT[C/G]TACTAAAAATACAAA | 84669 |
rs369304725 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60311558 | CCGGGCACAGTGGCT[C/G]ACGCCTGTAATCCCA | 84669 |
rs369341740 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60355986 | TAGCTTTGAAAACCA[A/G]AAATCTCCCTAAGCT | 84669 |
rs369352327 | snp | G/T | 1.72958e-05 | 0.00294068 | missense | USP32 | GRCh38.p7 | 17:60211111 | CCTTCATACCAATGG[G/T]ATTTGTCCTAGAAGT | 84669 |
rs369359022 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60390025 | GTCTCAAAAAAAAAA[-/A]CATAAATTCATTCCA | 84669 |
rs369371338 | snp | C/G | 1.65064e-05 | 0.00287279 | intron-variant | USP32 | GRCh38.p7 | 17:60255267 | GACCCATCTGAAACA[C/G]AGACACTCATGTTAG | 84669 |
rs369389081 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60304784 | AGGAAATTACGTGAC[C/T]TTAGTAATCTAGTGT | 84669 |
rs369400858 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60344747 | GGCATAAGCCAACAT[A/C]CCCAGCCAATAAATT | 84669 |
rs369416726 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60229779 | CTCACTTCTATATTC[C/T]ATTTATATAAAGTTG | 84669 |
rs369427451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60285644 | TAGTTATAATACAAA[C/G]ATGAATAGGATAAAT | 84669 |
rs369431852 | snp | A/G | 8.23662e-05 | 0.00641688 | missense | USP32 | GRCh38.p7 | 17:60226089 | GAAATGTTGTCTGAA[A/G]ATTTCTCTTCTGTAG | 84669 |
rs369438586 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177642 | CTTGAAACTATAAAG[C/T]ATGCATTTTGTCTGA | 84669 |
rs369440271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60307903 | AACGCACAAGTGGCT[A/G]GACGTCCAGAGGAAC | 84669 |
rs369446285 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60360883 | CCTATAATCCCAGCA[C/G]TTTGGGAGGCCAAGG | 84669 |
rs369449397 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60203559 | TACTTGATCTAGAAG[C/G]CTTGCTTTCCTTTAT | 84669 |
rs369452774 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191735 | AGGATGGTCTCAATC[G/T]CCTGACCTCTTGATC | 84669 |
rs369454822 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60225681 | TGGGGAGGCCAGGCA[C/T]GGTGGCTCACGCCTG | 84669 |
rs369481476 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60199709 | AGCCTCTATTTCATA[C/T]GTTACTATTATTATA | 84669 |
rs369510624 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60248084 | GCTTTGTAGTGTATT[C/T]TGAAGTCAGGTAGTA | 84669 |
rs369519575 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60180019 | AGTTTTTGCATTAAC[-/T]TAACTCCTGTTTTTT | 84669 |
rs369524618 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60199114 | GAGTGAGACCTGTCT[A/C]AAAAAAAAAAAGAAA | 84669 |
rs369544599 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60382611 | TTAAAATCACCTGGA[-/A]TTATTTAGAACCAAG | 84669 |
rs369582879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354563 | GCTTGGTGCAGCTGA[C/T]CTGAAGTAAATTAAC | 84669 |
rs369593109 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60399439 | GCGGGAGGATTGCTT[A/G]AGTCCAGGAGTTTGA | 84669 |
rs369594951 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373049 | GCATGCACCCATAGT[C/T]GCAGCTACTCTATAG | 84669 |
rs369598182 | snp | C/T | 0.000165093 | 0.009084 | missense | USP32 | GRCh38.p7 | 17:60192926 | GATAGCCCATACTGT[C/T]GTCACTGAAACAGAA | 84669 |
rs369601989 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60360828 | TCTTCTTCTAAATTC[A/C]AACAGTATACATAAA | 84669 |
rs369627051 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | USP32 | GRCh38.p7 | 17:60391841 | CCAGGCTGCCCGTCG[C/T]GGGCCTCCCAGGCAG | 84669 |
rs369657111 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60198851 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 84669 |
rs369657269 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60318362 | TGATTAAAGAATTAT[A/G]TATTCTCCTGTTCAC | 84669 |
rs369658730 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407848 | CACGCATGTAATTCC[A/G]GCACTTTGGGAGGCC | 84669 |
rs369661265 | snp | C/T | | | missense | USP32 | GRCh38.p7 | 17:60222485 | GGGACCATTTCATAG[C/T]CTCTTCCATGAATCA | 84669 |
rs369668745 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60264100 | AACATTACTAATAAA[C/T]GTTACCAAACTAAAT | 84669 |
rs369686734 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60210597 | CAGGCGTGAGCCCCT[A/G]CGCCCAGCCTACTTC | 84669 |
rs369731467 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60185828 | GCACTTTAGGAGGCC[A/G]AGGTGGGGTAATTGC | 84669 |
rs369737494 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60375000 | TAATTTGAAAAAAGA[A/G]TAACAGCAAATAATT | 84669 |
rs369742898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413395 | CCCAGATGGCTTACA[A/G]GTAAGGGTTTTTAAA | 84669 |
rs369758772 | in-del | -/TTTTTTAACAACGTACTGACTGTAAGTTAGAGACAAATATTTGTTTCACCTCATTGCATATGAACCAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60249857 | ATCACGATACTTTTT[lengthTooLong]CCTGAATCATCCTTT | 84669 |
rs369768456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60399107 | CAGGAAGCCTAGGGA[A/G]TGTGAATCTCGAAAG | 84669 |
rs369785538 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60385559 | CAAAAATAAATAAAT[A/G]GGCCAGAAGCAGTGG | 84669 |
rs369818801 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60386807 | AATATATTTATCTCC[C/T]CTTGTCAGAGACACA | 84669 |
rs369821093 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60289846 | ATCCTAATAGACATG[C/G]TAAAGAATACGAATA | 84669 |
rs369849688 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60236036 | TATTTAAGTTGGAGC[A/T]TTTTATTATTGGCTG | 84669 |
rs369856095 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60330913 | TCCCCTCCATTCCAG[A/G]CAAGTTTCCAAGTCA | 84669 |
rs369875236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60242910 | TAGCTTGTCAATTTA[C/T]AGAAAAAAGCTGGGA | 84669 |
rs369885560 | in-del | -/CACT | | | intron-variant | USP32 | GRCh38.p7 | 17:60329505 | TTTGAGATGAGGTCT[-/CACT]ATGTTGCCCAGGCTG | 84669 |
rs369916515 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60210387 | TGCGATCTTGGCTCA[C/T]TGCAAACACCACCTC | 84669 |
rs369928680 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60331427 | CAAGTTAGCCAGGCA[G/T]AGTGGCATGCACTTG | 84669 |
rs369932312 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60360170 | ACCGCGCCCGGCCCT[A/G]TAAGACAAAGATCCT | 84669 |
rs369948090 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407234 | AAGAAGGTATGCAAA[A/G]ACCTTCAGAAATTTG | 84669 |
rs369980525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401365 | ACAGAGTGAGACTCC[A/G]TCTCAATTAAAAAGA | 84669 |
rs369981691 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60381123 | AGCACAGCAGCACTA[A/G]GTAGTCCCATTTATT | 84669 |
rs369987526 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | USP32 | GRCh38.p7 | 17:60180505 | CCAGTTCTGTTGATA[C/T]TCTGTTTCTAACTTT | 84669 |
rs369998546 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60347244 | GGCTGGAGTGCAGTG[A/G]CATGATCTCAGGTCA | 84669 |
rs370007112 | snp | C/T | 0.000166575 | 0.00912468 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265478 | CATATGTAATTCCTT[C/T]AAAAATAACCCAAAG | 84669 |
rs370032347 | in-del | -/AA | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60396634 | CCAGGAGTTTGAGAT[-/AA]AGAGTGCCTAAAATT | 84669 |
rs370035825 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60247922 | ACCTCCTGACGTCAT[A/G]ATCCACCTACCTCAG | 84669 |
rs370048466 | snp | C/T | | | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60392130 | GCCTCCATGCCGGAT[C/T]ACGTGACTCTTCCGC | 84669 |
rs370061347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60197345 | TGTGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 84669 |
rs370074248 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60379198 | CATGTATTTGTATAC[C/T]AGAAAAACATACCTT | 84669 |
rs370111897 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60197544 | AGGAGGTGGAGGCTG[C/G]AGTAAGCCAGGATCG | 84669 |
rs370120680 | snp | G/T | 1.67022e-05 | 0.00288978 | synonymous-codon | USP32 | GRCh38.p7 | 17:60214712 | TGATGGTCTGCATTC[G/T]ACTAAAACAGCCTGT | 84669 |
rs370145880 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60379908 | ATTTGTGCTTAAAAC[A/G]GTCCAATGTGGTTTT | 84669 |
rs370187178 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60205161 | TGCCTCTTAATATAC[A/G]GATAAGGAATGTCAT | 84669 |
rs370187966 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366759 | TTGGTTTTTTTTTTT[-/T]CATGCTGCTTTTCTT | 84669 |
rs370198825 | in-del | -/GAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60372866 | AAAAAAAAAAAAAAA[-/GAC]AAAAAAATGGTTCAC | 84669 |
rs370200221 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60366051 | GGCGCGATCTCGGCT[A/C]ACCGCAACCTCTGCC | 84669 |
rs370205538 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60386364 | TTTTAGTTCATAAAT[A/T]AAAAAAAAAAAAAAA | 84669 |
rs370216444 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60313548 | AGTATAAATTCCTGA[A/C]GTCTAAGCAAAGAAC | 84669 |
rs370231460 | snp | C/T | | | upstream-variant-2KB, intron-variant, missense | C17orf64, USP32 | GRCh38.p7 | 17:60422345 | GTCTTCGCTCGACCC[C/T]GCACATCTTGCTCCG | 84669 |
rs370249902 | in-del | -/CA | 0.00914312 | 0.0669923 | intron-variant | USP32 | GRCh38.p7 | 17:60183809 | GAAGTTCAAATTCAC[-/CA]CATTGTACCCCTTGT | 84669 |
rs370269344 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60319841 | AACTATTCACGTAGT[A/T]TTTACATTGCAATAG | 84669 |
rs370271552 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410045 | AAAACTAACAAACTA[G/T]CTACAAAGTTAAAAT | 84669 |
rs370316129 | snp | G/T | 3.3018e-05 | 0.00406299 | missense, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179274 | TGTAACACACAGTAC[G/T]TTTTGTAATCAGACT | 84669 |
rs370320380 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60242779 | TCCAGTACTTGATTA[A/G]TGTATCCTTAGGTAA | 84669 |
rs370334080 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60327280 | GGCCGCTGACGTCAC[A/G]CCAGCTGCAGCAGGG | 84669 |
rs370340186 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60302820 | AAATATTTTTTAACA[C/T]TCTCAGAAATAAGTA | 84669 |
rs370347211 | in-del | -/T | 0.411074 | 0.191194 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232547 | GAAAGAGAAATTTGA[-/T]TTTTTTTTTTTTTTT | 84669 |
rs370363946 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409847 | AAGCTTAAAAAAATC[-/A]CAAAAAAACCCTCAA | 84669 |
rs370364236 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60369047 | TCGCCCAGGCTGGAG[A/T]GCAGTGGCGGGATCT | 84669 |
rs370375384 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60336522 | AGATCGAGACCATCC[C/T]GGCTAAAACGGTGAA | 84669 |
rs370387508 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395321 | TTCTAAAAATTGTGA[A/G]TTGAGATAGCAGATT | 84669 |
rs370399036 | snp | C/G | 0.000201444 | 0.010034 | intron-variant | USP32 | GRCh38.p7 | 17:60206988 | AAATATTTAAAGGAG[C/G]AATCATGAGAAGGAG | 84669 |
rs370423254 | snp | C/T | 0.000299003 | 0.0122234 | intron-variant | USP32 | GRCh38.p7 | 17:60288510 | CAGAAAACAATGAAA[C/T]GTCATTACTTACAAT | 84669 |
rs370534709 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179224 | GTCATCTCCCTCACC[A/G]CCAAGCTGTCTAGCA | 84669 |
rs370535147 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60188031 | TGTTACCCAGGCTGG[A/G]GTGCACTGGCGAGAT | 84669 |
rs370536336 | in-del | -/ACGCACCACCGTG | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60351573 | GCTGGGAGTACAGGC[-/ACGCACCACCGTG]CCTGGCTAATTCTTG | 84669 |
rs370559220 | in-del | -/TTC | | | intron-variant | USP32 | GRCh38.p7 | 17:60379865 | ACTGTAACCATATGG[-/TTC]TTCTCTCAATCATCA | 84669 |
rs370561663 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60243820 | TGCTGTTGGCTGAAG[A/G]GTTCTGTTGGTGGGT | 84669 |
rs370567424 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60314288 | CTGGGGCTACAGGTG[C/T]ATACCACTACTCCTG | 84669 |
rs370576528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302026 | ATATTTAACACTTTA[C/T]TATAAAATCTGATTT | 84669 |
rs370586600 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60192623 | TATGTTTAGTAGAGA[C/T]GAGGTTTTACTAGGT | 84669 |
rs370589910 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60347092 | CTGGAAGCAATAGCC[C/T]GCTACTACAAGAAAA | 84669 |
rs370624262 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60287447 | CCTTTAAAAACCCTT[-/A]ACCCATGAGCCTTGG | 84669 |
rs370626032 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60383213 | GGTCGCACTCCAGCC[G/T]GGGAAGCGACAGACA | 84669 |
rs370626879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60355000 | AGTGAGCCGAGATAG[C/T]GCCACCGCACCCCAG | 84669 |
rs370630001 | snp | C/T | 8.094e-05 | 0.00636109 | intron-variant | USP32 | GRCh38.p7 | 17:60301567 | TATTCTGTACATAGA[C/T]GAATTATTTTTGAGA | 84669 |
rs370632718 | snp | A/G | 0.00026383 | 0.0114824 | intron-variant | USP32 | GRCh38.p7 | 17:60236113 | AATCCTGTGAAAAAT[A/G]TAAATAGACAGGAAT | 84669 |
rs370645063 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60261475 | AACATGGCAAAACCC[A/G]TCTCTACTAAAAATA | 84669 |
rs370648457 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60379941 | AAAAGGTTACTCTTC[-/A]AGCAGCTTTCAATCT | 84669 |
rs370667204 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60243431 | AAGTATCCTTTCCTG[A/C]TCTTATGGGAAAAGC | 84669 |
rs370708574 | snp | A/T | 0.000100205 | 0.00707762 | missense | USP32 | GRCh38.p7 | 17:60205467 | TTCGGTGGACTGCAA[A/T]GATGTAACCTGTAAA | 84669 |
rs370724878 | snp | G/T | | | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402643 | CATGAGTATACCTGT[G/T]CTACTGTGATTCTGG | 84669 |
rs370741513 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415078 | ATAAATTTTTCGTTA[C/T]TTTCATGCTTGGGGA | 84669 |
rs370773686 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60364871 | GAGATTCATCTTCTA[C/T]ATACAAGTCAAACCT | 84669 |
rs370775792 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60375904 | TGAGCCACTATGCCC[A/G]GCCAAATCTTTAATT | 84669 |
rs370779753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60345802 | GCCTGGACAATGTGG[C/T]GAAACCCCATCTCTA | 84669 |
rs370780466 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60238746 | GAGGCAGAGTTTGCA[C/G]TGAGTCGAGATCATG | 84669 |
rs370784919 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60266988 | GAGACGGGATTTCAC[C/T]ATGTTGGCCAGGCTG | 84669 |
rs370802411 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60361901 | GCCTCAATGCTCAAT[A/G]TTAACACAAAGATAT | 84669 |
rs370804673 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60324284 | AAGACCGTGTTTCAA[-/AT]ATATATATATATATA | 84669 |
rs370806335 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60332562 | CTGAAGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 84669 |
rs370809148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60212278 | CATCATTAGGTGATT[C/T]TGTCTTTGTGTGAAC | 84669 |
rs370813482 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60307987 | ACCAGCAGAACGATG[C/T]GGAGTTAGGGTGGGG | 84669 |
rs370822104 | snp | A/C | 0.000153988 | 0.00877328 | missense | USP32 | GRCh38.p7 | 17:60236174 | CTGTTGCCACCACTG[A/C]ATGGAGATGATAAAC | 84669 |
rs370845007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60376674 | GATTACAGGTGCCTG[A/C]CATCACGCCCAGCTA | 84669 |
rs370852579 | snp | C/T | 0.00174543 | 0.0294901 | intron-variant | USP32 | GRCh38.p7 | 17:60211544 | ATGAGAACCAAAGCT[C/T]AGCTGTAGTAATATG | 84669 |
rs370860544 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60322951 | CAAAACCACAATGAG[A/C]CACAACTTCATACCC | 84669 |
rs370868832 | snp | A/G | 1.66776e-05 | 0.00288765 | intron-variant | USP32 | GRCh38.p7 | 17:60205409 | TTCACAAATGACACT[A/G]GCAAGACTGGCAGTG | 84669 |
rs370922683 | snp | C/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420660 | ATAAGAGCAAAACTC[C/T]GTCTCAAAAACAAAC | 84669 |
rs370934164 | snp | A/G | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421585 | AGGTGGCTCGAGTGA[A/G]GAAACTGCGGGGGCA | 84669 |
rs370948080 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60215174 | CAGGGTCTTGGCCAT[A/G]TTGCCCTGGCTGGTC | 84669 |
rs370977771 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60320614 | AAACCACACAGTGGC[A/C]CTGGCCAGAAATTGA | 84669 |
rs370981499 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60211371 | AGTGACTCCAGAAAG[A/T]TTACCTGTTGAGTTC | 84669 |
rs370982978 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377903 | TTGTTTAAGTTCAAA[A/G]CTACATACATTATTT | 84669 |
rs370986882 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201371 | CGAATATTCTTGTAC[A/C/G]TATCTCCTGGTACAC | 84669 |
rs370992615 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60333171 | CTGAGTATAACTTTG[A/G]ACTCCAGAAAAGCTT | 84669 |
rs371005378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281277 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 84669 |
rs371016912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60389542 | AGCGAGACTCTGTCT[C/T]GAGAAAAAAAAAAGC | 84669 |
rs371031167 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60225286 | GGCAAAACCCTATCC[C/T]TAAAATAAAAACACA | 84669 |
rs371035983 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60284300 | CTCACTGCAACCCCC[A/G]CCTCCCAGGTTCAAG | 84669 |
rs371054189 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178439 | AGCATGGGTGGGGCC[A/G]GGGGTGCAGAATACA | 84669 |
rs371066801 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | USP32 | GRCh38.p7 | 17:60198405 | CAAAGAGGCTGGGGC[A/G]ATTCTTCTGAGATGA | 84669 |
rs371069109 | snp | C/G | 1.64844e-05 | 0.00287087 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271383 | GAATAGGTGGTGAAA[C/G]CAATGGGCCAAATGT | 84669 |
rs371079197 | snp | C/T | 0.00361835 | 0.0423802 | intron-variant | USP32 | GRCh38.p7 | 17:60213702 | TTGTTATTTGGTTAG[C/T]AAACTTGAAACAAAT | 84669 |
rs371080591 | in-del | -/CT | | | intron-variant | USP32 | GRCh38.p7 | 17:60226479 | ATAAAGTAATTTACA[-/CT]CTATTCTGTTGGCAG | 84669 |
rs371109741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60340297 | AATTACCAGCCCTGC[C/T]AAGCTCAGTGGCTCA | 84669 |
rs371138189 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60234528 | GTCAGGAGATTGAGA[C/T]CATCCTGGCTAACAC | 84669 |
rs371142691 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60389913 | TCCCAGCTGCTGGGG[A/G]GGCTGAGGCAGGAGA | 84669 |
rs371145376 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | USP32 | GRCh38.p7 | 17:60288611 | TCCAGATAGAAGCCA[C/T]CGAGAGAAAGTAAAA | 84669 |
rs371153949 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60205802 | AATAATTCTAGATTT[A/G]TTGGAAGATTTTAAT | 84669 |
rs371155883 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | USP32 | GRCh38.p7 | 17:60255143 | GTACTGGTACTACTA[C/T]CCTCTGTTGCTGTCA | 84669 |
rs371165038 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416001 | CGTGCCACCACGCCC[A/G]GCTAATTTTTGTATT | 84669 |
rs371170528 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60276513 | CAAGTAGTAGATCAG[C/T]ATACAAAAAAATCTA | 84669 |
rs371179835 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60394447 | TTGGGAGCAAATTAA[C/T]GTATCTCTTTGTGGC | 84669 |
rs371220364 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60200717 | ACAAAGGTAACTATT[-/A]TTCTAAATGTTACAG | 84669 |
rs371222677 | snp | A/G | 1.70458e-05 | 0.00291935 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265366 | CATCCCAAATGGAGT[A/G]CATGATATTTTTAGA | 84669 |
rs371245807 | snp | C/T | 0.000778126 | 0.0197093 | intron-variant | USP32 | GRCh38.p7 | 17:60222361 | AAAGTAACAGAAGAC[C/T]CCCATCTATGACTGC | 84669 |
rs371267597 | snp | G/T | 0.000646022 | 0.0179609 | intron-variant | USP32 | GRCh38.p7 | 17:60223404 | GTTTAGATGTAAAAT[G/T]ACTTACCTTTACTGG | 84669 |
rs371289102 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306341 | TTTGTTTTAAAATCC[C/T]TATAATAATTTTCTG | 84669 |
rs371310250 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60385426 | TGGCACACGCCTGTA[A/G]TCCCAGCTACTTTGG | 84669 |
rs371317551 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60360059 | ATTTTTAGTAGAAAC[A/G]GGGTTTCACCATGTT | 84669 |
rs371320019 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60329024 | TGGATGGAAAAAGCC[C/T]AGCGGGCCCAGACAA | 84669 |
rs371326550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60278640 | GAAAGGTTTATACCA[C/T]GGACCCAAGATAAAA | 84669 |
rs371351324 | snp | A/G | 1.66369e-05 | 0.00288412 | missense | USP32 | GRCh38.p7 | 17:60181613 | TCTTTACTACTTGAC[A/G]GTTTATTTTTGCTGC | 84669 |
rs371363287 | in-del | -/A | | | frameshift-variant, intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422626 | AAGGGGGTGAAGGGG[-/A]ACAAGCCACTAGAGC | 84669 |
rs371371293 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60370019 | CCTGGGATTACAGGT[A/G]TAAGCCAGCGTGCAC | 84669 |
rs371373829 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60271713 | GAAATCTACAATTCC[C/G]CATTTAAGTAGGCTG | 84669 |
rs371378674 | snp | C/T | 3.29478e-05 | 0.00405867 | synonymous-codon | USP32 | GRCh38.p7 | 17:60236153 | GTATTTGACATATTC[C/T]TTCCACTGTTGCCAC | 84669 |
rs371386521 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60335203 | GGTCTTAAACTCCTG[A/G]GCTCAAGCAATCCTT | 84669 |
rs371388811 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60309593 | GGCAATGAAGTGAGA[A/C]ACTTTCTAAAAAAAA | 84669 |
rs371389912 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60276331 | TTATTTAAAAGGAGA[C/G]AGTATTTTAAAATTT | 84669 |
rs371406100 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60308812 | GCATGCCTGTAATCC[C/T]AGCTACTCAGGAGGC | 84669 |
rs371416520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413797 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 84669 |
rs371425177 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60363855 | GTTGGTTCCTTTGTT[C/T]TTGGGAGAAGGAAGG | 84669 |
rs371434911 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | USP32 | GRCh38.p7 | 17:60181418 | TTTCCAAGCTGACCA[C/T]TGCTGTAGCCATTGC | 84669 |
rs371442410 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60251468 | CCAGAAACCCAAGCC[A/G]GAAGAAACTACTGAA | 84669 |
rs371512688 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60275257 | AGGTCAGGAGTACAA[A/G]ACCAGCCTAGGAAAC | 84669 |
rs371534849 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60328024 | GGGAGCCATGGATGG[C/T]GGCAGGCAGCAGACA | 84669 |
rs371541924 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305755 | TTCACTGACTTTAAT[A/T]CAAAGAGTAAAGCAG | 84669 |
rs371564004 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60384926 | CAGCCTGGACAACAC[A/G]GCGAAACCCCATCTC | 84669 |
rs371582167 | in-del | -/TCTA | 0.0166325 | 0.0896639 | intron-variant | USP32 | GRCh38.p7 | 17:60375407 | AATATAGATTTACTC[-/TCTA]TCTTAGTAATTTTCA | 84669 |
rs371602577 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60297453 | TTCCTTTTCTTTTTT[-/C]TTTTTTTCTTTTTGA | 84669 |
rs371609933 | snp | C/T | 3.54824e-05 | 0.00421188 | missense | USP32 | GRCh38.p7 | 17:60208180 | AGTCTTAGTCCATAC[C/T]GTACAGGGGTAGTAC | 84669 |
rs371615403 | in-del | -/GT | | | intron-variant | USP32 | GRCh38.p7 | 17:60294384 | CAGGTTCCTGCAGGA[-/GT]GTGTGTGTGTGTGTG | 84669 |
rs371619130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60398185 | GCTTGGGCAACATAC[A/G]GAGACTCTGTCTCTA | 84669 |
rs371645431 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60234177 | GGAGTGCAGTGACGC[A/G]ATCTCGGCTCACTGC | 84669 |
rs371646002 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233453 | CAACAAAGGAAGATC[C/T]TGTCTCAACAAACAA | 84669 |
rs371649312 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60262472 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 84669 |
rs371693483 | in-del | -/GAATGGCTGAACCTCTGT | | | intron-variant | USP32 | GRCh38.p7 | 17:60355870 | AAGAAAAAAAAAAAA[-/GAATGGCTGAACCTCTGT]AAAAAAAAAAAAAAA | 84669 |
rs371697800 | snp | G/T | 0.000133485 | 0.00816851 | missense | USP32 | GRCh38.p7 | 17:60185483 | GTGGAAGCCTCCAGA[G/T]ATCCAGCTTCTTTGT | 84669 |
rs371709060 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60309748 | AAATCTCACCCATTA[C/T]ATCGAAAAGCAGGCA | 84669 |
rs371710851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60299911 | ACACAGGGGAAAATA[C/T]AAAGGGTCTCTCTGG | 84669 |
rs371740311 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407503 | GCTAGAACTGCTTAA[C/T]GAAGCTTAAAAACTA | 84669 |
rs371741213 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60334814 | TTCAAGGGTCAACTG[C/T]GTCTAGCTTTAGCAG | 84669 |
rs371741727 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60301180 | TTTGTGTGTGTGTGG[A/T]AAACATATGTATTAA | 84669 |
rs371763825 | snp | C/G/T | 4.94265e-05 | 0.00497104 | synonymous-codon, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266024 | TTCTAAAAGTGCAAC[C/G/T]ACCATGTCTCTCAGT | 84669 |
rs371771908 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60340886 | ACAAAATCTCTCACC[A/G]TTTGCTTGTCTGTAA | 84669 |
rs371772297 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60349625 | TATATATATATATAT[A/T]ATATATATATATATA | 84669 |
rs371773555 | in-del | -/TG/TGTG | | | intron-variant | USP32 | GRCh38.p7 | 17:60291537 | CTCTCTGTGTGTGTA[-/TG/TGTG]TGTGTGTGTGTGTGT | 84669 |
rs371774753 | snp | A/G | 1.70708e-05 | 0.00292149 | intron-variant | USP32 | GRCh38.p7 | 17:60226241 | GGCATCCTAAAATCA[A/G]GAAATCAGAGAATAA | 84669 |
rs371811691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289069 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 84669 |
rs371822482 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60202404 | TCTTGGTTATTCCTG[A/G]TGCTTTGTATTTCCA | 84669 |
rs371870407 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60227826 | TGTCTGTTACCACTG[-/G]CTTCACTTTAGTAGC | 84669 |
rs371875479 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60331770 | AGGCATAGTGGCATG[A/C]ACTTGTAGTCCCAGC | 84669 |
rs371898175 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60215818 | TAGTGCGGTGCGGCA[A/G]TCATGGCTCACTGCA | 84669 |
rs371922089 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60321631 | GAAATGAGGGCAAAC[A/C/G]TTCTTGAAATGAATG | 84669 |
rs371922158 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373384 | AAACACTGTGCAATT[C/T]GGTTACACCAAATTT | 84669 |
rs371927846 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60282423 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAACCTC | 84669 |
rs371930184 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60382115 | TCCAGAGGCTGGCAT[A/C]GTGAGATAAGCTCAC | 84669 |
rs371936680 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60284214 | AAGATTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 84669 |
rs371938852 | in-del | -/GTGGCAGCAGCCAGTGTGTCT | | | intron-variant | USP32 | GRCh38.p7 | 17:60328865 | GGAGCTACCTGCTCT[-/GTGGCAGCAGCCAGTGTGTCT]TGACTGCACACTGGC | 84669 |
rs371941594 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411085 | TGTAATCTCAGCACT[C/T]TGGGAGGCCGAGGCA | 84669 |
rs371948547 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60309535 | TGAGTCCAGGAGGCC[A/C/G]ATGTTGCAGTGGGCC | 84669 |
rs371954734 | snp | C/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421977 | GGCACTGGCGGGGAT[C/T]TTTATACACCCCCAA | 84669 |
rs371967092 | snp | C/T | 0.000132371 | 0.00813438 | intron-variant | USP32 | GRCh38.p7 | 17:60198496 | ACAGGCCTCTGATTC[C/T]TCCCTTTAGTTCTTC | 84669 |
rs371976160 | snp | C/G | 3.30136e-05 | 0.00406273 | intron-variant | USP32 | GRCh38.p7 | 17:60345438 | TTTAGGCTGGTGGAG[C/G]TGGATAACTACCTCA | 84669 |
rs372001057 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60283518 | ATAATGATGGCACCA[-/AT]AGAAAGAAAGATGCA | 84669 |
rs372010240 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60268159 | AACATGCTAACAATT[A/G]GAACACCAGTGCTTT | 84669 |
rs372022132 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60207242 | CTTTCATCCGTAAAA[C/T]CAACGAGATGATTGA | 84669 |
rs372048159 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308656 | AACTAGGCTGGATGC[A/G]GTGGCTCATGTCTGG | 84669 |
rs372048257 | in-del | -/TAGCTC | | | intron-variant | USP32 | GRCh38.p7 | 17:60328918 | ACCCCACTCTAGCTC[-/TAGCTC]ACACACCCCTCCCCA | 84669 |
rs372061701 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60344374 | ACCTCGTGATTCACC[C/T]GCCTCGGCCTCCCAA | 84669 |
rs372062002 | in-del | -/CCTCA | | | intron-variant | USP32 | GRCh38.p7 | 17:60327511 | CCCCACCCCACCTCA[-/CCTCA]GGAGCCAGGCTGAGC | 84669 |
rs372067227 | in-del | -/TAGTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60365049 | ATTCCTTATGCCTTT[-/TAGTT]AAGAAATCATGTTAT | 84669 |
rs372103553 | snp | C/T | 1.64743e-05 | 0.00287 | missense | USP32 | GRCh38.p7 | 17:60222521 | GGAGTTCGTTTTAAT[C/T]GTCCTCCTTCTAGTG | 84669 |
rs372106775 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60333043 | CTCAATGAAAAAAAA[-/A]TTACTGGTATCATAA | 84669 |
rs372161163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60379178 | GATATGAGAAAAGCT[G/T]CATACATGTATTTGT | 84669 |
rs372182842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60391830 | TTACCCACCCTCCAG[A/G]CTGCCCGTCGCGGGC | 84669 |
rs372194561 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60247428 | CAGGTGATCCAGCCG[C/T]CTCGGCCTCCCAAAG | 84669 |
rs372198767 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60297169 | TTGGGATGCCAAGAC[A/G]AGAGAATCATTTGAG | 84669 |
rs372199010 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60284340 | TGCCTCTGCCTCCCA[A/C]GTAGCTGGGACTACA | 84669 |
rs372210715 | in-del | -/AGCACTGAGTGCT | | | intron-variant | USP32 | GRCh38.p7 | 17:60293856 | CAAAAGAAAATGGGC[-/AGCACTGAGTGCT]GCATGAAAGAATCAG | 84669 |
rs372215644 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60349578 | GACTCTGTCTCAAAA[A/G]AAAAAAAAAAAAAAA | 84669 |
rs372216477 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60325655 | TAAAGGGCCAGGCGC[A/G]GTGGCTCACACCTAT | 84669 |
rs372217675 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388665 | TTTCCTTGTGTTTTA[C/T]TCAAAATATTTAAGA | 84669 |
rs372218447 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60283988 | GGAACAGTAAAACTC[A/G]TAAGAAATAAGAAGA | 84669 |
rs372235807 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60189338 | AGAATTGGTAGTTTC[C/T]CCAGTCCTCCATAGC | 84669 |
rs372244335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228064 | AGAGTCAAGCTCTGT[C/T]GCCCAGGCTGGAGGT | 84669 |
rs372250183 | snp | A/G/T | 0.000414389 | 0.0143889 | intron-variant | USP32 | GRCh38.p7 | 17:60345656 | TCAGGAGAGAAAAGA[A/G/T]GTGTCTCATAATTTT | 84669 |
rs372258120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60329110 | AACAACACTGTACTC[C/T]ATAAATATGTATAAT | 84669 |
rs372280021 | snp | A/G | 0.000521074 | 0.0161327 | intron-variant | USP32 | GRCh38.p7 | 17:60185670 | CAGGTAGAGGGAACA[A/G]GAGGAAAGGGGTGCG | 84669 |
rs372296599 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP32 | GRCh38.p7 | 17:60190548 | CACCATTTTATGGTG[A/G]CCCTAAATACTTACC | 84669 |
rs372298185 | in-del | -/CT | | | intron-variant | USP32 | GRCh38.p7 | 17:60249068 | TCTTTTTTATTATCT[-/CT]GTTTTTATTTTTAAG | 84669 |
rs372300794 | snp | C/T | 8.27712e-05 | 0.00643263 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294760 | CCATTTCTTCCCGTA[C/T]AACATAGTTCCCAGA | 84669 |
rs372315529 | in-del | -/TAC | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295755 | ATATTGTTATAATAT[-/TAC]TATTTTATTATTGTT | 84669 |
rs372365914 | in-del | -/C | 0.0137398 | 0.081738 | intron-variant | USP32 | GRCh38.p7 | 17:60255298 | GAACATCTTTTTTTT[-/C]TTTTTTTTTTTTTTT | 84669 |
rs372376073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194728 | AATACAAACTTTTCT[A/G]CCTCCAAAATCTCAA | 84669 |
rs372377838 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60342690 | ATCTCAGACTGCTGC[A/G]CTAACAGTGAGCAAG | 84669 |
rs372387966 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60304108 | TAATCCCAAAAACCA[A/G]CTAGACAAATCACAT | 84669 |
rs372392595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60401181 | AAAAAAAAGACCGGG[C/T]GCAATGGCTCACACC | 84669 |
rs372399235 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60187705 | AAGGCTGATAAAAAA[-/A]CATATTTGTGGACTG | 84669 |
rs372433134 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210421 | GGTTCAAGCGTTTCT[A/C/T]GTGCCTCAGCCTCCC | 84669 |
rs372461081 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60247078 | GGCTGACTGTGCTTT[C/T]GAGGTATTATACAGT | 84669 |
rs372544692 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60374588 | ACAGGTTTTCACCAT[A/G]TTGCCCAGGCTGGTC | 84669 |
rs372578712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405262 | GGCTGGAGTGCAGTG[A/G]CTCAATCTCGGCTCA | 84669 |
rs372581720 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377818 | AGGGTTCTTTCTATT[A/C/G]TGGTTTTCTGCAGCT | 84669 |
rs372593471 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417950 | GTCCACCACCACGTC[C/T]GGCTAATCTTTTTTT | 84669 |
rs372600143 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60384859 | ACGCCTGTAATTCCA[A/G]CATTTTGGGAGGTGG | 84669 |
rs372637043 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60239429 | CCCTTTCCTTCTCTC[A/T]CCTTTCCTAAGATTC | 84669 |
rs372639179 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60176982 | GGAGCAAGGGGGAGC[A/G]GCTCTAAATACAGCT | 84669 |
rs372645224 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60229255 | ATGTTACCCAGACTG[A/G]TCTCAAACTCCTGGA | 84669 |
rs372646185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418787 | ATCACTGGTCATTAA[A/G]GAAATGCAAATCAAA | 84669 |
rs372693592 | in-del | -/A | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404040 | GCGAGACCCTGCCTC[-/A]AAAAAAAAAAAAAAG | 84669 |
rs372701894 | snp | A/G | 1.65026e-05 | 0.00287246 | intron-variant | USP32 | GRCh38.p7 | 17:60236095 | AAGTCTCACGCAGCT[A/G]AAAATCCTGTGAAAA | 84669 |
rs372726448 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60212411 | AAGTGTAACACAATG[G/T]TAAGTATTTGTGTAT | 84669 |
rs372763366 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256118 | CTGAGGCAAGAGGAT[C/T]GCTTGAGCCCAGGAG | 84669 |
rs372783410 | snp | C/T | 4.95266e-05 | 0.00497603 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265960 | ACGCAACAAGACATA[C/T]ACAATCATAACTTAC | 84669 |
rs372788029 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60184008 | GGTCTACCCGTCAGC[A/C]GGGCGCAGTGGCTCA | 84669 |
rs372794533 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60324387 | CTACTAACTTGATTC[A/G]AAAAAGACTATCTCA | 84669 |
rs372797261 | snp | A/G | 0.00127194 | 0.0251864 | intron-variant | USP32 | GRCh38.p7 | 17:60214573 | ACTATTTAAAATTAA[A/G]CAAATACCAACAATC | 84669 |
rs372803199 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60398628 | TTCATAAAGCACTTT[G/T]TGTGTGCTAAATCCT | 84669 |
rs372842707 | snp | C/T | 1.66067e-05 | 0.00288151 | missense | USP32 | GRCh38.p7 | 17:60205487 | TAACCTGTAAAGGGG[C/T]TGTCAGGAAGAGATG | 84669 |
rs372855983 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60275178 | ATGAGAAGTATTGGC[C/T]GGGCGCGGTGGCTCA | 84669 |
rs372868611 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60371977 | AGCTGTGAATCCTAC[A/G]CATATGCTCATAAGG | 84669 |
rs372879550 | snp | C/T | 1.6492e-05 | 0.00287154 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271421 | TCAAATCGTCCAGTC[C/T]GGGATTGAGCCTTCA | 84669 |
rs372894634 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60384177 | AATAGTGATGCCATT[C/T]GCTGTCATGGGAAAG | 84669 |
rs372895602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289575 | GTTTCTTTGCTTTCT[C/T]TCCAGGTATTTTTCT | 84669 |
rs372906080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60182919 | GCACTGTGTGAAGTG[C/T]TTTACTCTCCATGTG | 84669 |
rs372910497 | snp | C/T | 0.000131781 | 0.00811621 | synonymous-codon | USP32 | GRCh38.p7 | 17:60226139 | GCTTCCAATTCTATC[C/T]TCGACCTGCTCCATA | 84669 |
rs372916908 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60274533 | AAAAGGAGCAAGATG[A/G]GGGAAAAACACATTA | 84669 |
rs372940106 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60214283 | TAATCTTTGTAACAT[A/G]TAATCTTTATATGTA | 84669 |
rs372941030 | in-del | -/T | 0.49753 | 0.0350569 | intron-variant | USP32 | GRCh38.p7 | 17:60347352 | ACCACACCTGGCTCA[-/T]TTTTTTTTTTTTTTT | 84669 |
rs372943119 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60240685 | AGGTCTTTTCTGAGT[A/G]TGTATCTTGTTGTTG | 84669 |
rs372945955 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60199774 | ATATTTTATAAAATT[G/T]TAAAACGTAGCTAAA | 84669 |
rs372949507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257336 | GGATCACATGTGCCA[A/G]TTGGGGGGAGTCAGT | 84669 |
rs372967075 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60204759 | TAGATGTGAGCCACC[A/G]CACCTGGCCATTTTC | 84669 |
rs373005384 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60262317 | CTGCGTCAGCCTCCT[A/G]AGTAGCTGGAATTAC | 84669 |
rs373010552 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60400240 | GAAATTCTGAGATTA[C/T]AGGCGTGAGCCACCA | 84669 |
rs373035470 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60257274 | GGTAGAAGGAGAGGA[A/C/T]TGGAAAGTCCTTCGG | 84669 |
rs373045436 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305241 | GCTCAGCTTCTCATG[A/G]GGCCTCAGAAAGCTT | 84669 |
rs373050968 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60356060 | GTTTAGAGCTTCTCA[A/G]AAGAAGTGTCAATAT | 84669 |
rs373056704 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60344950 | ACTACAGGGACGCAC[A/C]GTGGCGCCGGTTAAA | 84669 |
rs373071780 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60192032 | TGGCGTGGTGGCTCA[C/T]ACCTATAATCCCAGC | 84669 |
rs373080318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60196739 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 84669 |
rs373112638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60317675 | TCAAGAATTAGCTAG[A/G]TGTAGTGCCATGCAC | 84669 |
rs373128009 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60362608 | CATGGAGAGAATGTC[C/T]TTAAGTATTCATTAG | 84669 |
rs373132189 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60221021 | CAGGCTTTATTTTCC[G/T]TTACTCTCATAACCA | 84669 |
rs373140559 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60229040 | TCAACTTTTTTTTTT[-/T]CACTTATGCTTTTTG | 84669 |
rs373140967 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60364013 | CTGTTCAGGCTGCTA[A/C]AACAAAATATCTCAG | 84669 |
rs373143266 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177965 | TATTAAAAAACTACA[C/T]GAAAAAAATGCTACC | 84669 |
rs373175572 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60387674 | TTGATACAACTTACA[A/G]TGAGATTACCTCCCA | 84669 |
rs373180452 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60311640 | CCAGCCTGGCCAACA[G/T]GGTGAAACCCTGTCT | 84669 |
rs373184186 | snp | A/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422809 | TCAGAAGTTTATGCA[A/T]GACCTGTGTTCCTGG | 84669 |
rs373196276 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60367981 | AATCTAGAGATAACA[A/G]GAGGCTCTGCTTAGG | 84669 |
rs373227690 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60318380 | TTCTCCTGTTCACTA[A/G]TCTAATTCCATCTAG | 84669 |
rs373242290 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60371254 | CTGTCTCTAAAAATT[-/A]AAAAAAAAAAAAAAA | 84669 |
rs373254080 | snp | C/T | 0.000100323 | 0.00708176 | missense, intron-variant | USP32 | GRCh38.p7 | 17:60391887 | CCCCCCTCACCTCTC[C/T]TCAGCGCCTCCTCGT | 84669 |
rs373263908 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60386948 | ACTACTTAAAAACTG[C/T]CCCATTTTTCTCCTT | 84669 |
rs373268706 | snp | A/G | 6.70017e-05 | 0.0057876 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265395 | GAAAAAGATAAATTA[A/G]TTCTATCTAGACTCA | 84669 |
rs373281525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60326543 | ACCTTGGGTGATCCA[C/T]CCACCTTGGCCTCCC | 84669 |
rs373301136 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408332 | GATGGAACTTCTAGT[A/G]GTGAAAAATACAGTA | 84669 |
rs373302817 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60270043 | GATACACTATGCAAC[A/C]TAAGAGAAAGAAATT | 84669 |
rs373307373 | snp | C/T | 3.30912e-05 | 0.00406749 | intron-variant | USP32 | GRCh38.p7 | 17:60255277 | AAACAGAGACACTCA[C/T]GTTAGGAACATCTTT | 84669 |
rs373308604 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60300584 | CCTTTTACAAATAAC[A/G]TATATAAAATGTTAT | 84669 |
rs373314363 | snp | C/G | 3.3761e-05 | 0.00410845 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179226 | CATCTCCCTCACCGC[C/G]AAGCTGTCTAGCAGC | 84669 |
rs373315452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60247768 | GGCTCATTGCAACCT[A/C]CACCTCCCCAGTTCA | 84669 |
rs373322786 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60191332 | GCTTGAACCTGGGAG[A/G]TGGAGGTTGCAGTGA | 84669 |
rs373333392 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60241917 | ATAAACTGTGCTTTT[G/T]GTGTTATATCTATGA | 84669 |
rs373335526 | in-del | -/AATT | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60301511 | CTTTGGGAAAATGTC[-/AATT]CAAATCCTCTACCTG | 84669 |
rs373360716 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60332614 | GATCATGCCATTGCA[C/T]TCCAGCCTGGGCAAC | 84669 |
rs373364290 | in-del | -/C | 0.338976 | 0.23363 | intron-variant | USP32 | GRCh38.p7 | 17:60228501 | TTCTTTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT | 84669 |
rs373374469 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392422 | TCGCAGCCGCGCGCC[C/G]CGCCCGGGCGCCTCC | 84669 |
rs373418553 | snp | A/G | 1.67713e-05 | 0.00289575 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269450 | GTTTAACACACTTAC[A/G]TTTTTGTCTTTCAGC | 84669 |
rs373427496 | snp | G/T | | | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231020 | GGTTTTCAGAAGATA[G/T]ATTTCTAAATAGGTA | 84669 |
rs373433760 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410381 | ATCCTTTAAAAACCC[C/T]AGCCTCGGTGGGCGC | 84669 |
rs373437186 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312436 | TTGTTGTCGTTGTCG[C/T]TGTTGTTGAGACAGG | 84669 |
rs373481105 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60212171 | TTGCTTTTTTTTTTT[-/A]AAAGACATCTTATTC | 84669 |
rs373489871 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | USP32 | GRCh38.p7 | 17:60345534 | CCCGGATGAAGCAGT[A/G]CTGGCCCATGTAATA | 84669 |
rs373493631 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60379919 | AAACAGTCCAATGTG[A/G]TTTTAAAAAAAGGTT | 84669 |
rs373497180 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60247973 | ACAGGCGTGAGCCAC[C/G]ACGCCTGGCCTGGAT | 84669 |
rs373498551 | snp | A/G | | | synonymous-codon | USP32 | GRCh38.p7 | 17:60211441 | CTGTGTGTTACTAAC[A/G]CACTGGATGCTTGAG | 84669 |
rs373499281 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60266584 | ACCTCTGCCTCCCGA[A/G]TTCAAGTAATTCTCC | 84669 |
rs373499425 | snp | A/C | | | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402152 | ACAAGCACTAATATA[A/C]GGATCTTTCATTCTA | 84669 |
rs373507068 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60293114 | ATTCTATATAAAATA[A/T]CAAGATTCAGATTTT | 84669 |
rs373507590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60361296 | TCAGATCTTTTTCCA[C/T]GCTTTTATAAGATGT | 84669 |
rs373512628 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60345217 | GAATAAGAAGCCAAT[C/G]ATGGAAATGTTCCTA | 84669 |
rs373514364 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60248737 | TTTAAATACAGCTTC[A/G]TTTAGCTCTTTGAAA | 84669 |
rs373519844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332185 | CTCGCTTGAACCTGG[A/G]AGGTGGAGGTTGAGG | 84669 |
rs373535143 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60307615 | AAACTTACTAAAAAC[C/G]TATAGTAACCACAAC | 84669 |
rs373562033 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60389269 | GATTCTGGGGACAGC[C/T]GCAGTGGCTCACCTG | 84669 |
rs373568592 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60195159 | AACCCACTCCAATCT[C/G]TACTCCCTTATCTAT | 84669 |
rs373576333 | snp | A/T | 1.66682e-05 | 0.00288684 | intron-variant | USP32 | GRCh38.p7 | 17:60190732 | ATAATTATGAAGGAA[A/T]CTAAATTTTCTTAAT | 84669 |
rs373577151 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60354096 | AAAGGTAAGCTTTTT[C/T]CTTGAAGTTCAATAC | 84669 |
rs373598648 | snp | A/G | 8.26644e-05 | 0.00642848 | intron-variant | USP32 | GRCh38.p7 | 17:60214822 | GCAGATGTGAAAAAG[A/G]AGCACCCCTCTCAGC | 84669 |
rs373603783 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409081 | AGCCGGGCACAGTGG[C/T]TCATGCCTGTAATCC | 84669 |
rs373605350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60243745 | TGCTGACTAACTGCT[A/G]GCCTAGTATATGGTC | 84669 |
rs373617076 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60301249 | ACACACAGTAACAAC[A/G]TTTAACAATTTGAGG | 84669 |
rs373655607 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60188109 | CCTCAGCCTCCCAAG[C/T]AGCTGGGACTACAGG | 84669 |
rs373688349 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60199961 | AGCACTTCAGGAGGC[C/T]GAGGCGGGCGGATCA | 84669 |
rs373700541 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60245082 | TCACTCATATAAGAT[C/T]GTTATATGTAATGGG | 84669 |
rs373726178 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60369081 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG | 84669 |
rs373747605 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414859 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTAGATG | 84669 |
rs373773963 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60351547 | AATTCTCCTGCCCAG[C/T]CTCCCAAGTAGCTGG | 84669 |
rs373774007 | snp | C/T | 0.000135421 | 0.00822753 | intron-variant | USP32 | GRCh38.p7 | 17:60252456 | ACCTAGGGAAAAAAA[C/T]GGTAAATCAAAGTTT | 84669 |
rs373774045 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60397385 | TTGTTGTTTAAGACA[C/T]AGCGTCTCTCTCTAT | 84669 |
rs373778149 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60199404 | AGATATTTACGATAT[-/T]CCTTAATATAGAGAT | 84669 |
rs373790617 | in-del | -/TG | | | intron-variant | USP32 | GRCh38.p7 | 17:60291538 | CTCTCTGTGTGTGTA[-/TG]TGTGTGTGTGTGTGT | 84669 |
rs373799936 | in-del | -/T | 0.459233 | 0.136827 | intron-variant | USP32 | GRCh38.p7 | 17:60222678 | GCTGGAAAAACTTAA[-/T]TTTTTTTTTTTTTTT | 84669 |
rs373810267 | in-del | -/T | 0.0158531 | 0.0876085 | intron-variant | USP32 | GRCh38.p7 | 17:60207918 | TTGGAAAACTTGGCA[-/T]TTTTTTGTTGTTGTT | 84669 |
rs373810890 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60246414 | GTATATATATATATA[-/T]TTTTTTTTTTTCTTT | 84669 |
rs373817056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60316612 | TTGGGAGGCTGAGAC[A/G]GGGGGAGCACTTGAG | 84669 |
rs373817173 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60215013 | TTGTTATGTTGCCAG[A/G]CTAGAGTGCGGTGCT | 84669 |
rs373820842 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60380716 | AAAGCTCCTAAAATT[A/G]CATGGAATTTTGACA | 84669 |
rs373826877 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60310181 | AAATTAGAACAGCTA[C/T]GGCTGTTCCTCAAAA | 84669 |
rs373827007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60337309 | GTCTAAAAACACTCC[A/G]GAATCTAATACGGCT | 84669 |
rs373830260 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60202033 | TGTATTTACCAGTAT[C/T]ATCTTCCAAGGGCTG | 84669 |
rs373836052 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60338807 | TTATTTTCCATTTAC[C/T]TTGTTTTCTCAATCC | 84669 |
rs373839089 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60365931 | CTATGTGGGGTTTTT[C/T]GGTTCATTTTTGGTT | 84669 |
rs373843469 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295825 | TCATAGATACATATG[C/T]ATAGGAAGAAACGGT | 84669 |
rs373850668 | snp | C/T | 0.00247037 | 0.0350583 | intron-variant | USP32 | GRCh38.p7 | 17:60209330 | TTGTGGCCAGAACAT[C/T]TTGTCTATTGCTTAC | 84669 |
rs373857260 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421302 | AACATGCTGGCATAG[A/T]GGACAAGTTAAAAAG | 84669 |
rs373863672 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60238485 | CCAGCCTGGGCAACA[C/T]GGCAAACCCTCATCT | 84669 |
rs373872267 | snp | C/T | 3.52808e-05 | 0.0041999 | intron-variant | USP32 | GRCh38.p7 | 17:60208024 | GTCATCTTTGGAGGA[C/T]AGAATCAAAAGTTTC | 84669 |
rs373873268 | snp | C/T | 0.000149109 | 0.00863321 | intron-variant | USP32 | GRCh38.p7 | 17:60271326 | TTACCAGTGAACATA[C/T]GTAGAAAATGGAATG | 84669 |
rs373876348 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393157 | CCGTGGCAACCGCTG[C/T]CCTACTATCAATTTC | 84669 |
rs373888511 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60227231 | TAATATTATTGCCTT[C/T]TATTTCTGGCAAGCG | 84669 |
rs373889767 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | USP32 | GRCh38.p7 | 17:60222541 | TCCTTCTAGTGTTAA[C/T]GATGTAGCCTGAGAA | 84669 |
rs373892347 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60253520 | TCTATAATCCTAGCA[C/T]TTTGGGAGGCTGAGG | 84669 |
rs373973853 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60332051 | AGTTCAAGATCAGTT[C/T]TGGCAACATAGCGAA | 84669 |
rs373981258 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413824 | GAGCTGAGATCGCAC[C/T]GCTGCACTCCAGCCT | 84669 |
rs373991637 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60369211 | GTTTTAGCTGGGATG[C/G]TCTCGATCTCCTGAC | 84669 |
rs374016227 | snp | C/T | 0.000153988 | 0.00877328 | missense | USP32 | GRCh38.p7 | 17:60183411 | TTTTCTGTGATTTTA[C/T]CCACCGACCATTTAC | 84669 |
rs374017334 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60310054 | ATCAAGGAAAAAAAA[A/C]AGAAAGAAAAAGAAA | 84669 |
rs374020126 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395073 | TTAACAATGGTATTT[A/G]TGTATCTAAACATAG | 84669 |
rs374026543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60182279 | AACCTTTAGAACTTT[C/T]ATGTGAATTTTATCT | 84669 |
rs374029668 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60261607 | GCCGAGATCATTCCA[C/T]TGCACTCCAGCCTGG | 84669 |
rs374050025 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60207468 | GAGGTGAGAGTGTGT[C/T]CAGAAATCCCAAAGA | 84669 |
rs374080183 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60258041 | AATGGAAGAAGAAAA[A/C]AGGGAGCAAGCAGAT | 84669 |
rs374091620 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60187643 | TGATTTTTATTGACT[A/G]TATTTTCTGTGGAAC | 84669 |
rs374130483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60366182 | TCTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 84669 |
rs374137536 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60192379 | TTTGGTATGGACTGT[A/G]GTTTATAAAACCAGC | 84669 |
rs374138818 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60216330 | AACCCTGGTTAACTA[C/T]TCCGCCAAAAATCTA | 84669 |
rs374140453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60337961 | AAAATGTTGTGCTAT[A/G]TACTACAGATTCAGG | 84669 |
rs374141192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410440 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACAAGGT | 84669 |
rs374143180 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60381432 | GGTGACAGAGGGAGA[C/T]CCTGTCTCAAAAAAA | 84669 |
rs374145465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60311544 | AGGGTAGATGTAGGC[C/T]GGGCACAGTGGCTCA | 84669 |
rs374168836 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60371253 | TCTGTCTCTAAAAAT[A/T]AAAAAAAAAAAAAAA | 84669 |
rs374173955 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60325995 | AAAAAAAAAAAAAAG[A/T]AAAAATATTTAGAAC | 84669 |
rs374183916 | snp | A/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404458 | CCAACTTGATTTTTA[A/T]ACCAAACCTTTAGTT | 84669 |
rs374214644 | in-del | -/TTA | 0.0221141 | 0.102801 | intron-variant | USP32 | GRCh38.p7 | 17:60280089 | GGTAAATTGAGTAAG[-/TTA]TTATTATTATTATTA | 84669 |
rs374232665 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60394551 | ATACTCAGGAATTAA[C/T]AGAATATGACCGCAT | 84669 |
rs374245722 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60368829 | AACATTTCCCAAACA[A/G]CCAAACCAAAACAAA | 84669 |
rs374250123 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60340445 | TCTTTGTCTCTTTTG[A/T]TCGTTGTTGGTTTAA | 84669 |
rs374268757 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60347491 | CCCGAGTAGCTGGGA[C/T]TACAGGCGCCCGCCA | 84669 |
rs374271482 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60180411 | TGTTCCTTTAATACT[C/G]ACAGCATCTATATAT | 84669 |
rs374306740 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60250454 | CTATAATAAATTAGA[C/T]TGTAATATTCTAAGA | 84669 |
rs374347100 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60325972 | GTAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs374386562 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60237120 | AAATCTACTCTATCT[A/C]TCTATCTATCTATCT | 84669 |
rs374394383 | snp | C/G | 0.221439 | 0.248363 | intron-variant | USP32 | GRCh38.p7 | 17:60334609 | AGGCAGGAGAATGGC[C/G]TGAACCCGGGAGGCG | 84669 |
rs374397238 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60309555 | TGCAGTGGGCCAAGA[C/T]TGCACTACTGCTCTC | 84669 |
rs374460845 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60192527 | GGAACCGCTGCCTCC[G/T]GGGTTCAAGCGATTC | 84669 |
rs374471773 | snp | C/T | 1.64841e-05 | 0.00287085 | synonymous-codon | USP32 | GRCh38.p7 | 17:60209499 | TTCTTGGGAGTCCTG[C/T]TGCTGAAACCCATTA | 84669 |
rs374473506 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60210301 | TTAGTTTCATTCATT[C/G]ATCCTTCTACTTTTT | 84669 |
rs374476139 | snp | A/C | 6.99815e-05 | 0.00591488 | intron-variant | USP32 | GRCh38.p7 | 17:60255287 | ACTCATGTTAGGAAC[A/C]TCTTTTTTTTCTTTT | 84669 |
rs374479254 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60199114 | AGTGAGACCTGTCTC[-/A]AAAAAAAAAAAGAAA | 84669 |
rs374479993 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60249311 | CAACTAGGGAAGAAT[A/G]AAGTGCTAAAGCCCA | 84669 |
rs374486747 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416006 | CACCACGCCCAGCTA[A/G]TTTTTGTATTTTTAG | 84669 |
rs374556637 | snp | C/T | 0.000810822 | 0.0201185 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265946 | CATTGGAAGTTTATA[C/T]GCAACAAGACATACA | 84669 |
rs374562270 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60297896 | TGTTCCACAAGCCGT[-/T]AACTACAGCTTTGAC | 84669 |
rs374584121 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60421767 | TTTCCGCCCTCGGCC[C/T]CGGGTCCCTGGAGGG | 84669 |
rs374592512 | snp | G/T | 0.000153988 | 0.00877328 | missense, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179316 | TCCATACTGCTTGTG[G/T]CTGCCATCTTTTTGC | 84669 |
rs374611702 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60221895 | CGAGTGCTGTTTACC[A/G]TGTAAGCACAACAAA | 84669 |
rs374614024 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60363973 | TGATTCTCGTGCACT[A/G]TTATTCCCCCAAAAC | 84669 |
rs374646129 | in-del | -/CCAAGGAGTAA | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404850 | ACAATCTCCAAACAA[-/CCAAGGAGTAA]TCACTACTAAATGTC | 84669 |
rs374667113 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60391372 | CTCAAGAGACAGGCA[C/T]AGGCTCTGGGAAAAG | 84669 |
rs374668536 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309107 | GTAATACTTCAAAAG[A/G]GCAAATAACAAAAGC | 84669 |
rs374678378 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60269802 | GTCCATCTATATTTA[C/G/T]CTTACATCATTTTTA | 84669 |
rs374684056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60300414 | TATCTTCCCTTTCAC[A/T]TTTAGCAGGGGAAAT | 84669 |
rs374693916 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60190970 | GGCAAATAAATGACA[C/T]GGGAATTGCCTGTTT | 84669 |
rs374697109 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403652 | AATGAGTTTATTTAA[A/G]GAAAGGGGGTCGTGA | 84669 |
rs374768366 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60332579 | CTTGAACCCAGGAGG[C/T]GGAGACTGCAGTGAG | 84669 |
rs374770652 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60340571 | TGTACGACTTTGCAC[A/G]TGAGATGGGTCTCCT | 84669 |
rs374785497 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60239363 | GAGCTTTTTGAACGC[A/G]TAGGTTCACGTCTTA | 84669 |
rs374786424 | snp | G/T | 1.6473e-05 | 0.00286988 | missense | USP32 | GRCh38.p7 | 17:60236195 | GATGATAAACCAGTT[G/T]TGTCCTGCTTGCAGA | 84669 |
rs374795865 | in-del | -/TGC | | | intron-variant | USP32 | GRCh38.p7 | 17:60314894 | TGTAATCAGAAACAA[-/TGC]AAGCCACAAGACAAC | 84669 |
rs374800917 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60194874 | GAAATCCTCACTTGC[C/G]TCTTTACCCACTGTC | 84669 |
rs374809102 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60336587 | CGGGCGTAGTGGCGG[A/G]CGCCTGTAGTCCCAG | 84669 |
rs374814162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413249 | CTTATCCCTGTGTTA[C/T]AGAACTGGGGTCCAC | 84669 |
rs374815270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60188510 | AAATGTTCACATATC[A/G]TAAGCTTGTTCCCAT | 84669 |
rs374819776 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392449 | CTCCGCTGGCGACGG[G/T]GGGTGGTGACTTCCG | 84669 |
rs374826839 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60334899 | CTCCTGACCTCGTGA[G/T]CCACCTGCCTCGGCC | 84669 |
rs374828929 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60212343 | TATGGTATAGGCTGT[C/T]GCTCCTTGGCTACAA | 84669 |
rs374846523 | snp | A/G | 0.000801255 | 0.0199996 | intron-variant | USP32 | GRCh38.p7 | 17:60207182 | TGTTTCAGATAAAAT[A/G]GAAAAGTTCTCTCTC | 84669 |
rs374928984 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60190388 | AATGAACTCCAGAAG[A/C/T]TGGAAAATGAAAAAG | 84669 |
rs374936210 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60247522 | GTGTATGGTAAGAAA[C/T]TGGGAACTGGTTTCA | 84669 |
rs374970137 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60363072 | AGGAGGGAAGATCAC[-/AT]GAGACCAAGAGTTCA | 84669 |
rs374972949 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60359582 | TTGGGAGGCTGAGAT[A/G]AGAGGATCACTTGAG | 84669 |
rs374976239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196546 | ATAACTTATTTTGGC[C/T]GGGCACGATGGCTCA | 84669 |
rs374979967 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60221344 | GTTATTTTTCATAAA[C/T]GTAATTATTAAGAAC | 84669 |
rs374986468 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60349176 | ATAATTAATCTAATA[C/T]ATTAATTATATATTA | 84669 |
rs374999861 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60327469 | TCCACAAAGGCAGCG[A/G]GACCCAGGGACAAGC | 84669 |
rs375012516 | snp | C/T | 0.000212664 | 0.0103096 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294852 | CAAAGACCAAATATA[C/T]GTTGGTGGAAGTAGG | 84669 |
rs375064519 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60279314 | CATGATGAGATCCCA[C/T]CTCTACAAATAATTT | 84669 |
rs375064537 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366211 | TCGCCTAGGCTGGAG[G/T]GCAGTGGCGCGATCT | 84669 |
rs375066429 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60301366 | TCCTCAACACTTATT[A/T]TCAGGCTTTTTACTT | 84669 |
rs375091046 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60284214 | AAGATTTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 84669 |
rs375099637 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60340910 | TCTGTAAAGGATTTT[A/G]TTTCTCCTTCACTTA | 84669 |
rs375124902 | in-del | -/AGAG | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424055 | GTGAGAGAGCAAGCA[-/AGAG]AGAGAGGAGGGCGTG | 84669 |
rs375134848 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60220528 | GATTTTTAAGTAGTT[G/T]TAACCTGCTTATAAG | 84669 |
rs375140834 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60225971 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAGA | 84669 |
rs375176709 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60368301 | TTAATGTAATTTTTT[-/T]AACGCAATAGAATGA | 84669 |
rs375197107 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60366548 | TAGGGTTACAGGTGT[A/G]AGCCACTGCACCCAG | 84669 |
rs375202764 | snp | A/G | 8.66378e-05 | 0.00658114 | missense | USP32 | GRCh38.p7 | 17:60181674 | TCCTCCCCAAAGTCC[A/G]TGGGCTGCTATTAGG | 84669 |
rs375214681 | snp | A/G | 1.72475e-05 | 0.00293657 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391981 | TCGGAGCCTGATCTC[A/G]CCCCCACCCCCCTCC | 84669 |
rs375244696 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP32 | GRCh38.p7 | 17:60180681 | TTAGCAGTTAACTGT[A/G]CTATGGCCAGGGTAT | 84669 |
rs375258519 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60331834 | GCTTGGGGAGGTCAA[C/T]GCTGCAGTGAGCTGT | 84669 |
rs375264532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60213965 | TTTTTTTTTTAAAGA[C/T]GGAGTCTGGCTCTGT | 84669 |
rs375275315 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378285 | TAATTGAAAGAAAAC[-/AG]AAAATAACAAGTATT | 84669 |
rs375291822 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60318664 | GGGACTAGGTCAGGT[A/G]AATTTACAGAATTGT | 84669 |
rs375302441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417557 | CTCCCAGGTTCAAGC[A/G]TTTCTCCTGCCTCAG | 84669 |
rs375321127 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60352426 | AGATGACCATGGAAC[A/T]GCCATATGACCCTTG | 84669 |
rs375326495 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60355845 | CAAAAAAAAAAAAAA[A/G]AGAGAGAGAAAGAAA | 84669 |
rs375327977 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60243865 | TTATCATAATAAAAT[A/G]TCTCTCTGGCTCCAG | 84669 |
rs375331086 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60273213 | CCTGGCCTCAAGTGA[C/T]CTGTCTGCCTCGGCC | 84669 |
rs375332911 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60327099 | ACAACAATTGGTTGT[A/G]TATTTTCAAATAGCT | 84669 |
rs375337527 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60302205 | CAATGGCGTCATCTT[C/G]GCTCACTGCAACCTC | 84669 |
rs375337543 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405726 | CATGATCACACCACT[G/T]CATTCCTGCCTGGGC | 84669 |
rs375339995 | snp | A/G | 1.65138e-05 | 0.00287343 | synonymous-codon | USP32 | GRCh38.p7 | 17:60255184 | ACATACCTGGAAAAG[A/G]AGGTTCAAAAACTCA | 84669 |
rs375344640 | snp | A/G | 5.10174e-05 | 0.00505035 | intron-variant | USP32 | GRCh38.p7 | 17:60185685 | GGAGGAAAGGGGTGC[A/G]TGGGAAGGCATTTAA | 84669 |
rs375351066 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60376599 | GGCAATCTTGGCTCA[C/T]TGCAACCTCTGCCTC | 84669 |
rs375361797 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60322877 | AATATTTTCATTTCA[G/T]ATTTACTAGTCCATT | 84669 |
rs375369597 | snp | A/G | 0.00018149 | 0.00952428 | intron-variant | USP32 | GRCh38.p7 | 17:60198472 | ACAAGAGAATAGAGA[A/G]TTCAGAAGACAGGCC | 84669 |
rs375395453 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288909 | TCTGTATGTTAACTA[A/C/T]AAATTATTTCATCAA | 84669 |
rs375435948 | snp | A/G | 4.95659e-05 | 0.004978 | synonymous-codon, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60294731 | TTTACCATCCACCAC[A/G]TGGAGCATTCTTTCC | 84669 |
rs375445440 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182878 | GGACAAGACAGCAGC[G/T]ACCATTCCTGTTTAC | 84669 |
rs375463446 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60386071 | GAAAGAACAATAAAG[C/G]AAACACTTGAAAAGC | 84669 |
rs375508233 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | USP32 | GRCh38.p7 | 17:60183944 | AAACTGGATATTAAA[A/C]ATCTATGCTTTTAAT | 84669 |
rs375513472 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60185709 | CATTTAAAGTGGTGA[C/T]CTAGGTATGCATCAA | 84669 |
rs375513849 | snp | C/T | 0.000132433 | 0.00813627 | intron-variant | USP32 | GRCh38.p7 | 17:60190551 | CATTTTATGGTGGCC[C/T]TAAATACTTACCCTT | 84669 |
rs375537805 | snp | C/G | 6.61146e-05 | 0.00574917 | intron-variant | USP32 | GRCh38.p7 | 17:60214821 | GGCAGATGTGAAAAA[C/G]AAGCACCCCTCTCAG | 84669 |
rs375540859 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60289372 | TCCCTCTTCTTTAGC[A/G]CTCTTCAATCTGCCT | 84669 |
rs375548047 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245563 | TACACTTAGTTTTGA[C/T]ATATCAGTGTAACTG | 84669 |
rs375550445 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP32 | GRCh38.p7 | 17:60269569 | AAACCTGTAAAATAG[A/G]AAGAGATGCCATAAA | 84669 |
rs375567205 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60281451 | GCTGAGGCAGGAGAA[C/T]TGCTGGAACTCGGAG | 84669 |
rs375602393 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60193691 | TAAGAGTGGCATACT[G/T]TACAGCTCATCTGGC | 84669 |
rs375623047 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60349038 | ATTTTCATTAATGGC[C/T]TTAGTAACAAATTAG | 84669 |
rs375624385 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60200125 | CTTGAACGCAGGAGG[A/C]ATAGAGTACAGTGAG | 84669 |
rs375629402 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378573 | CAACAGATGGATGTA[C/T]AAACAAGATGTAGTA | 84669 |
rs375633282 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60247340 | GCCTGCCACCATACC[-/C]AACTAGTTTTTGTAC | 84669 |
rs375635046 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60250885 | TAGATTTTGCTTAAT[C/T]TTCTTTAAGAAATAA | 84669 |
rs375640848 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60335418 | TCCACAAAGTCCTAT[A/C]CAGTTCCTACATTCA | 84669 |
rs375641944 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60261932 | ATAATAGATACCACC[A/G]TACAGAATCATCATG | 84669 |
rs375643658 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60256105 | GCTACTCCAGAGGCT[-/G]AGGCAAGAGGATCGC | 84669 |
rs375649412 | snp | A/G | 6.60022e-05 | 0.00574428 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265964 | AACAAGACATACACA[A/G]TCATAACTTACAGGA | 84669 |
rs375650759 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178443 | TGGGTGGGGCCGGGG[G/T]TGCAGAATACATTTC | 84669 |
rs375659862 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60349997 | TGCTCTGTGGTTTTT[-/T]CGTTGTTGTTGGTTT | 84669 |
rs375661575 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60238804 | CGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 84669 |
rs375668742 | in-del | AA/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295241 | AAGAGCAAAACTTCG[AA/G]AAAAAAAAAAGATAA | 84669 |
rs375671859 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60307355 | ATCTGCCTGCCTTGG[C/T]CTCCCAAAGTGCTGG | 84669 |
rs375687153 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60351331 | TGCCCAAGTAGCTGG[A/G]ACTACAGGCATGCAC | 84669 |
rs375694727 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60240451 | AGAGGGAGAGAAGAA[A/G]AGAGAGAGGGAGGGA | 84669 |
rs375707036 | in-del | -/CAAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60297410 | AATCAATCAATCAAT[-/CAAT]AAACTATGTTCTAAC | 84669 |
rs375707787 | snp | G/T | 7.15743e-05 | 0.00598181 | intron-variant | USP32 | GRCh38.p7 | 17:60211559 | TAGCTGTAGTAATAT[G/T]CCATGGCACAAACAG | 84669 |
rs375720254 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421206 | AAAACAGACCTTCCA[A/T]CTTGGAGGCGGATAA | 84669 |
rs375766083 | snp | A/G | 1.64743e-05 | 0.00287 | missense | USP32 | GRCh38.p7 | 17:60222441 | GGTTTGCTCCATACC[A/G]GTGATAAAGTGCTCT | 84669 |
rs375776562 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60292275 | ACTCATTCTTCCAAC[C/G]TGTTTTCTATCTAAA | 84669 |
rs375777777 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328037 | GGCGGCAGGCAGCAG[A/G]CAGGCTCCTGGGCAG | 84669 |
rs375785521 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60254715 | AAATTAAAAATAATA[A/G]TGATAATAATAATAA | 84669 |
rs375786529 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60345111 | ATAGAATTAACTATG[C/T]TTTACTATACAGAAA | 84669 |
rs375803776 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60309950 | TCGGAAGTCTGAGGC[A/T]GGAGAACTGTTTGAA | 84669 |
rs375810780 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60329480 | AATTTGTTTTTATTT[A/T]TTTTTTTTTTTTGAG | 84669 |
rs375815162 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409669 | TTGCTTCTAACCTCA[A/G]AGCCACCCTTGTTCA | 84669 |
rs375819289 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60185306 | GTAGAAAGATTCATC[A/T]CTGTATTCAACATAA | 84669 |
rs375841770 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205576 | AGTGTTTGGCATTCC[A/G]TTGGGGATGAATATT | 84669 |
rs375841970 | in-del | -/TT | | | intron-variant | USP32 | GRCh38.p7 | 17:60371252 | CTCTGTCTCTAAAAA[-/TT]AAAAAAAAAAAAAAA | 84669 |
rs375896821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212868 | GACTGATTCTCGTGC[C/T]TCAGCTTCCTGAGTA | 84669 |
rs375903329 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60326347 | CAGAGTTTCGCTCTC[A/G]TCGCCCCGGCTCGAG | 84669 |
rs375905804 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60267871 | GCTGGAGTGCAATGG[C/T]GCAATCTTGGCTCAC | 84669 |
rs375913746 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60292434 | TAATTACAACTTTCT[C/T]GATATCCAACCCCCT | 84669 |
rs375913865 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60355971 | TCCCCAGCTATGCAA[C/T]AGCTTTGAAAACCAA | 84669 |
rs375914358 | in-del | -/GACC | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60355415 | AAAAACCTGTAAGGA[-/GACC]GACCGATTGCCGGAA | 84669 |
rs375915467 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60384204 | AAAGACTAGTGGAGG[A/C]CTATCTTGTTAGAAA | 84669 |
rs375923159 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408200 | AAATCAGGTGACAGA[A/C]ATGGACCCAGAAATG | 84669 |
rs375961125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60383046 | AGGTCAAGAAATGAA[A/G]ACCATCCTGGCCAAC | 84669 |
rs375964710 | snp | A/C/T | 0.000247078 | 0.0111121 | synonymous-codon, missense | USP32 | GRCh38.p7 | 17:60236162 | ATATTCTTTCCACTG[A/C/T]TGCCACCACTGCATG | 84669 |
rs376033149 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60244499 | TTCTTTTGTGGTAAA[C/T]AGGTATTTTCTAGGA | 84669 |
rs376036655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60187927 | TTTCATAGAAGACTA[C/T]TGAAAAAAAGAGAGT | 84669 |
rs376075675 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60238803 | AGCGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 84669 |
rs376085887 | snp | A/G | 0.000164079 | 0.00905608 | intron-variant | USP32 | GRCh38.p7 | 17:60223634 | TTTTAGTTATTATAC[A/G]TAAACAGGCTTGAGG | 84669 |
rs376086903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400114 | GGATTATAGGCATGC[A/G]CCACCATGCCTGGCT | 84669 |
rs376106661 | snp | A/C | 0.000132277 | 0.00813149 | missense | USP32 | GRCh38.p7 | 17:60205655 | GATGGCGAAGAGGAG[A/C]AATCTACAAATTCAA | 84669 |
rs376110989 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60375690 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 84669 |
rs376130568 | in-del | -/C | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232168 | ACTAATTTTCTTTTT[-/C]TTTTTTTTTTTTTTT | 84669 |
rs376147291 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305466 | ACACCTCCCACGAGG[C/T]CCCACCTCCAACATT | 84669 |
rs376162084 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377820 | GGTTCTTTCTATTCT[G/T]GTTTTCTGCAGCTGT | 84669 |
rs376168632 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60327421 | GGTGGGGGGCGGGGG[A/G]GAGGCGGAGCTGGGC | 84669 |
rs376172641 | in-del | -/GTAAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60326164 | ACTTTGATAAAATAA[-/GTAAA]TAAGTAAGATTTACT | 84669 |
rs376214408 | snp | A/G | 5.00563e-05 | 0.00500256 | synonymous-codon, intron-variant | USP32 | GRCh38.p7 | 17:60391931 | GATCCGTGACTCCTT[A/G]GCACCCATGCTCCCC | 84669 |
rs376216867 | snp | C/T | 3.38621e-05 | 0.0041146 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179223 | AGTCATCTCCCTCAC[C/T]GCCAAGCTGTCTAGC | 84669 |
rs376228034 | snp | A/C | 1.64982e-05 | 0.00287208 | missense | USP32 | GRCh38.p7 | 17:60223551 | GTTGTCGAGCAAAGC[A/C]AACATCTGCCCCTGG | 84669 |
rs376230220 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60363324 | GCTGGGCGTAGCGGC[A/G]TGCACCTGTAGTCCC | 84669 |
rs376232070 | snp | C/T | 0.000667223 | 0.0182528 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179247 | GTCTAGCAGCCAGAG[C/T]GGTAGCTTTACTGTA | 84669 |
rs376269459 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60368727 | TTCACAGTTGTCAGC[-/A]ATTTCCTAATAATCA | 84669 |
rs376290835 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308394 | GTTTGAACAGCAGGG[C/G]ACTGAAGAAGGGAGC | 84669 |
rs376352735 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | USP32 | GRCh38.p7 | 17:60226141 | TTCCAATTCTATCTT[C/T]GACCTGCTCCATAGG | 84669 |
rs376365944 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60272898 | TACTGAGTTTTGGCA[C/G]AATAGTAAGCTGTGT | 84669 |
rs376366511 | in-del | -/GAGA | | | intron-variant | USP32 | GRCh38.p7 | 17:60307491 | ATGACATTCTTCATA[-/GAGA]AAGAAAAAGAGAATC | 84669 |
rs376414431 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60262684 | CTACAGCCTTCAATA[-/A]TATGAATCTGTTATT | 84669 |
rs376417953 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60380814 | AGTCAAACCAAGGCT[C/T]ACCTTCAAAACCAGG | 84669 |
rs376427251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60287836 | AAAATTTCTCAGGCC[A/G]GGCATGGTGGCTCAC | 84669 |
rs376427853 | snp | C/T | 5.18309e-05 | 0.00509046 | intron-variant | USP32 | GRCh38.p7 | 17:60223361 | CTGAAATGAAATTTA[C/T]TAATAGCTTGCAAGA | 84669 |
rs376429066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210558 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 84669 |
rs376436759 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60205360 | AAGAGAAGAAAATAC[A/G]TTCAATGATGTTGCA | 84669 |
rs376456894 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60368601 | TATTACCAAAAAAAA[A/C]CCCACATACACACAA | 84669 |
rs376478706 | snp | A/C/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420383 | TAAAAAAGACTCTTT[A/C/T]CTGGCCGGACGCGGT | 84669 |
rs376490047 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60376622 | TCTGCCTCCCGGATT[C/T]AAGCAATTCTCCTGC | 84669 |
rs376555786 | snp | C/T | 1.6563e-05 | 0.00287771 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269519 | TCTCCTTAAAATCTA[C/T]GTGATTGTCACGATT | 84669 |
rs376573197 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418146 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 84669 |
rs376575764 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60238542 | GCGCAGTGCCTCACG[C/T]CTATAATCCCAGCAC | 84669 |
rs376579464 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60209714 | TCTTTTGAATCTTAA[-/T]GTCAAATGACCCCCC | 84669 |
rs376585619 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227271 | TCTTTTCTTTTTTTC[-/T]TTTTTTTTTTTTTTT | 84669 |
rs376608527 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60249857 | ATCACGATACTTTTT[C/T]TTTTTAACAACGTAC | 84669 |
rs376610860 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60268642 | GAGCAAATTGTAATG[A/G]AAACAACCAAGCCAG | 84669 |
rs376622399 | snp | A/G | 0.000153988 | 0.00877328 | missense | USP32 | GRCh38.p7 | 17:60345605 | TTTAGCTCTACATCT[A/G]TAACTGCAATTCAGA | 84669 |
rs376655891 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60243238 | TGCTGAACTCATTTT[-/T]ATTAATTCTAACAGT | 84669 |
rs376665624 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | USP32 | GRCh38.p7 | 17:60211411 | TCTCCCTGAGATAAA[A/G]TACTGTGTCAGTGGC | 84669 |
rs376669690 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60293241 | GAGTACTGGGTAGCC[A/T]ACCACCCTTAGTTTC | 84669 |
rs376670323 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60390405 | ACCTGTCAGGCTCAA[A/C]AGCATCCCGGAAATG | 84669 |
rs376674643 | snp | C/G/T | 3.30013e-05 | 0.00406199 | intron-variant | USP32 | GRCh38.p7 | 17:60345447 | GTGGAGGTGGATAAC[C/G/T]ACCTCAAAGGAAAAC | 84669 |
rs376675539 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60349602 | AAAAAAAAAAATATA[A/T]ATATATATATATATA | 84669 |
rs376678143 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290861 | TAATCAATCATGATC[A/G]CTAGCGAAGATGTCT | 84669 |
rs376684752 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60278616 | AAACAAGAAAAAGGA[A/T]CACCTATAGAAAGGT | 84669 |
rs376697408 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60339059 | GGATTACAGGAGCCC[A/G]CCACCACGCCCAGCT | 84669 |
rs376699082 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60388916 | TTAACATAACACTTC[-/G]TTTCCAAGGCCCCGC | 84669 |
rs376702836 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60367034 | GGGTTTCACCGTGTT[A/G]GCCAGGATGGTCTCA | 84669 |
rs376705882 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60398840 | AATTTAATTAGCTGG[G/T]TGTAGTGGTGTGTGC | 84669 |
rs376707392 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60289109 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 84669 |
rs376724230 | in-del | -/TG | 0.0010954 | 0.0233773 | intron-variant | USP32 | GRCh38.p7 | 17:60271308 | AGATGGGCTCAGGTA[-/TG]TTTACCAGTGAACAT | 84669 |
rs376754966 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60336444 | GAATTGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 84669 |
rs376780539 | snp | C/T | 3.29826e-05 | 0.00406082 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271367 | TCACTTAGAGATGGA[C/T]GAATAGGTGGTGAAA | 84669 |
rs376785313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60189380 | GAAAAGTCAGTTACC[A/G]TTACTAACTTATCCA | 84669 |
rs376816347 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60354335 | ATGCATTCTGATTTC[C/T]GTTATAGGATAGGAG | 84669 |
rs376822570 | snp | A/G | 0.000860001 | 0.0207186 | synonymous-codon | USP32 | GRCh38.p7 | 17:60301636 | GCCTCTTGTAAGGAG[A/G]ACAAGTCCAACTATT | 84669 |
rs376842196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347957 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAA | 84669 |
rs376845401 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309901 | ATATAAAAATTAGCC[A/G]GGCATGGTGGCATGT | 84669 |
rs376850378 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60204247 | AGCCATCCGCATTTA[C/T]GTGGCAGTGAAGATA | 84669 |
rs376863532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60226738 | AGTGGTGTATGTACA[C/T]AGAGTGAAGGGCAAT | 84669 |
rs376867266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60367062 | TCAATCTCCTGACCT[C/T]GTGATCCGCCCCCCT | 84669 |
rs376874537 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60349666 | TACATATATATACAC[-/AT]ATATATATATACACA | 84669 |
rs376880966 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60278162 | TCCTACCACAGCCTT[C/T]CAAAGTGCTGGGATT | 84669 |
rs376885618 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60300380 | CCCACGAAACAGACG[G/T]ACACTAAGCAACTAA | 84669 |
rs376908626 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60204888 | AAGTGATCCTCCTGC[C/T]TCAGCCTCCAGAGTA | 84669 |
rs376930511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413785 | CAGGAGAATCACTTG[A/G]ACCCAGGAGGCGGAG | 84669 |
rs376946656 | in-del | -/CA | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177521 | CAAACACAGATCAAA[-/CA]ACATTAGTAGATTGA | 84669 |
rs376952616 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60355870 | AAGAAAAAAAAAAAA[A/G]AATGGCTGAACCTCT | 84669 |
rs376984897 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60215112 | AGCTGGTACTACAGG[C/T]GCACGCCACCACATC | 84669 |
rs376999104 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60379899 | ATATGCTAAATTTGT[A/G]CTTAAAACAGTCCAA | 84669 |
rs377023063 | snp | C/T | 3.34102e-05 | 0.00408705 | missense | USP32 | GRCh38.p7 | 17:60214711 | TTGATGGTCTGCATT[C/T]GACTAAAACAGCCTG | 84669 |
rs377032408 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60263758 | GAGAGGAGAAAGAAG[A/G]GGACTGAATTGTCAA | 84669 |
rs377056105 | snp | A/G | 0.000373423 | 0.0136591 | intron-variant | USP32 | GRCh38.p7 | 17:60301568 | ATTCTGTACATAGAC[A/G]AATTATTTTTGAGAT | 84669 |
rs377061902 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60332744 | CAAGCTTCCTTTCAC[A/T]ATAGATTAGTTTGCA | 84669 |
rs377069337 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60374700 | AATAAATAGAAGGAG[C/T]ATACTCTAAAATAAT | 84669 |
rs377081743 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60283987 | GGGAACAGTAAAACT[C/T]GTAAGAAATAAGAAG | 84669 |
rs377095560 | snp | C/T | 1.76387e-05 | 0.00296969 | intron-variant | USP32 | GRCh38.p7 | 17:60181286 | CAAGTGAACAAAACA[C/T]AGACCACTCTCTGAA | 84669 |
rs377123457 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366392 | TTGAACTCCTGACCT[C/T]GTGATCTACCTGCCT | 84669 |
rs377134435 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420201 | GTTTTGCCATGTTGG[C/T]CAGGCTGGTCTCAAA | 84669 |
rs377136411 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392823 | CATCTCGCCTGCCCG[A/G]CCCACCTTCTCCTCC | 84669 |
rs377156228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60400056 | TGCAACCTCCACCTC[C/T]CAGGTTCAAGCAATT | 84669 |
rs377161843 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60182710 | AGAGGCTGCAGTGAG[C/G]TGTGATCTGTGTTGC | 84669 |
rs377165868 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60210373 | CTGGAGTACAGTGGT[A/G]CGATCTTGGCTCATT | 84669 |
rs377208612 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402375 | CCCACCTCAGCCTCC[C/T]GAGTAGCTGGGACCA | 84669 |
rs377219408 | in-del | -/GTGTGTGT | | | intron-variant | USP32 | GRCh38.p7 | 17:60294383 | CAGGTTCCTGCAGGA[-/GTGTGTGT]GTGTGTGTGTGTGTG | 84669 |
rs377249314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60298428 | TTTTTTCAGTTGACA[C/T]ATATAACCTATCCAC | 84669 |
rs377251395 | snp | C/T | 0.00109942 | 0.0234201 | intron-variant | USP32 | GRCh38.p7 | 17:60255302 | ATCTTTTTTTTCTTT[C/T]TTTTTTTTTTTTTGA | 84669 |
rs377254706 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60284428 | GGTTTCACCATATTG[A/G]CCAGGCTGGTCTCGA | 84669 |
rs377257156 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60221694 | TATTTTTATTAGACA[C/T]GGGGTTTCACTATGT | 84669 |
rs377265520 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60203532 | TCTCTTGTTGCTGCT[A/G]TACAATCAATTTACT | 84669 |
rs377273253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60312464 | AGGGTCTCATTCTAT[C/T]GCCCAGGCTGTAGTG | 84669 |
rs377277572 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306980 | CAGTTTAGCCAGAGA[C/T]GTGAAAGATCTATAA | 84669 |
rs377278378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60266844 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 84669 |
rs377291847 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360821 | AATGCATTCTTCTTC[C/T]AAATTCAAACAGTAT | 84669 |
rs377306317 | snp | C/T | 3.31225e-05 | 0.00406941 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265414 | TATCTAGACTCACCT[C/T]TGTGGTGTCATGTGC | 84669 |
rs377319911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60238671 | TTAGCTGGTGTAGTG[A/G]TGGGCACCTATAATC | 84669 |
rs377325827 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60327274 | TGGAGTGGCCGCTGA[C/T]GTCACGCCAGCTGCA | 84669 |
rs377326036 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393164 | AACCGCTGTCCTACT[A/G]TCAATTTCACTACTC | 84669 |
rs377336439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60383058 | GAAGACCATCCTGGC[C/T]AACATGCTGAAACCC | 84669 |
rs377342189 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60243991 | ATTCTTTTACTTTCA[A/C]CCTATTTGTGCCTTT | 84669 |
rs377345390 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60273522 | CACAAGTAACTTAAC[C/T]GCCTATCAAAATAAA | 84669 |
rs377389523 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60382381 | GCACACCTGTAGTCC[C/T]CACAATTCGGGAGAC | 84669 |
rs377389862 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181597 | GCTGGCATCCAAGTT[C/T]TCTTTACTACTTGAC | 84669 |
rs377396473 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60327075 | AGCACTATAGGGTGA[C/T]TATAATTAACAACAA | 84669 |
rs377398372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60230738 | TCCCCTTCCTACACG[C/T]TTATTTTTCTTGTTC | 84669 |
rs377409814 | snp | G/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177975 | CTACACGAAAAAAAT[G/T]CTACCTGAAATAAAT | 84669 |
rs377417081 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60376898 | GTTTTCTTCTATATA[G/T]GAAGTTATAAAATGC | 84669 |
rs377420779 | snp | C/T | 9.97954e-05 | 0.00706313 | intron-variant | USP32 | GRCh38.p7 | 17:60255280 | CAGAGACACTCATGT[C/T]AGGAACATCTTTTTT | 84669 |
rs377422791 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60389251 | TTTTTAGCTCTATCA[A/G]AAGATTCTGGGGACA | 84669 |
rs377450825 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60198059 | GGATTATTTGACACT[A/G]GAATGTTTGGCAAAA | 84669 |
rs377452831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267937 | TGCCTCAGCTTCTCA[A/G]GTAGCTGGGATTACA | 84669 |
rs377460032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60234614 | ACGTGCCTGTAGTCC[C/T]AGCTACTCGGGAGGC | 84669 |
rs377470304 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60379920 | AACAGTCCAATGTGG[C/T]TTTAAAAAAAGGTTA | 84669 |
rs377476435 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60351695 | GGCCTCGCAAAGTGC[C/T]GGGATTACAGGCGTG | 84669 |
rs377493057 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60394256 | GTTAGATTATCGTAA[C/T]TAATGGGAAGTGAAT | 84669 |
rs377505363 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60300789 | ACTCCTATGTAATTC[A/C]AGAACATTTTCGCCA | 84669 |
rs377537743 | in-del | -/GT | | | intron-variant | USP32 | GRCh38.p7 | 17:60325994 | AAAAAAAAAAAAAAA[-/GT]AAAAATATTTAGAAC | 84669 |
rs377538693 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60361892 | TGCCATTTGGCCTCA[A/G]TGCTCAATGTTAACA | 84669 |
rs377549701 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414906 | CCCAGGCTGGAGTGC[A/C]GTGGTGCAATCTCAG | 84669 |
rs377556401 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60387529 | ATACCATAAGCTAAT[C/G]ATTTATAAATGATAT | 84669 |
rs377559373 | in-del | -/CA | | | intron-variant | USP32 | GRCh38.p7 | 17:60239288 | TGGCTTTGTAAAATA[-/CA]GTTTCATTATAATGC | 84669 |
rs377613629 | in-del | -/CA/CACA/CACACA | | | intron-variant | USP32 | GRCh38.p7 | 17:60202443 | ATCAGCTTATCAAAT[-/CA/CACA/CACACA]CACACACACACACAC | 84669 |
rs377618714 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60284299 | GCTCACTGCAACCCC[C/T]GCCTCCCAGGTTCAA | 84669 |
rs377623009 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60248400 | GCTTCTAAGATTAAT[A/G]ATTTTCGAGAAATTT | 84669 |
rs377625284 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60386320 | TCAGTCCCACCTTAA[C/T]CTTCTCAGTACACTA | 84669 |
rs377651556 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395041 | GAGCCACCACGCCTG[C/G]GCTACAGTAGGTAAT | 84669 |
rs377653073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414100 | GGGCGTGGTGGCTCA[C/T]GCCTATAATCCCAGC | 84669 |
rs377659284 | snp | C/T | 3.30229e-05 | 0.0040633 | missense | USP32 | GRCh38.p7 | 17:60183210 | GTGAGGATGGGCTTT[C/T]GCTCAGGAGCACGTC | 84669 |
rs377671610 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60374399 | TTACAGTTAAGTTTT[-/G]TTTTTTTTTTTTTGA | 84669 |
rs377673346 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60243804 | TGAATATGTATTCTG[C/T]TGCTGTTGGCTGAAG | 84669 |
rs377689609 | snp | A/G | 1.70116e-05 | 0.00291642 | intron-variant | USP32 | GRCh38.p7 | 17:60192973 | TAAGAAGCATTTCTG[A/G]TTCGAGGTCCAACTC | 84669 |
rs377693012 | snp | C/G | 1.7093e-05 | 0.00292339 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265362 | GATACATCCCAAATG[C/G]AGTACATGATATTTT | 84669 |
rs377728607 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232162 | GTCAACACTAATTTT[C/T]TTTTTCTTTTTTTTT | 84669 |
rs377747179 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60238797 | CAACAGAGCGAGACT[C/G]CATCTCAAAAAAAAA | 84669 |
rs386798142 | multinucleotide-polymorphism | AG/CA | | | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177041 | GTTCCTAACAGGCCA[AG/CA]GATGGTACTGGTCTG | 84669 |
rs386798143 | multinucleotide-polymorphism | GC/TT | | | intron-variant | USP32 | GRCh38.p7 | 17:60226854 | ACTTGAGGTCAGGAG[GC/TT]CAAAATGGTGAAATC | 84669 |
rs386798144 | in-del | AGA/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60240495 | AAAGAGAAAAAAGGG[AGA/G]GAGAGAGAGAGAGAG | 84669 |
rs386798145 | multinucleotide-polymorphism | GGC/TGT | | | intron-variant | USP32 | GRCh38.p7 | 17:60284266 | TCGCCCAGGCTGGAG[GGC/TGT]AGTGGCATGATCTTG | 84669 |
rs386798146 | multinucleotide-polymorphism | AC/GT | | | intron-variant | USP32 | GRCh38.p7 | 17:60284267 | CGCCCAGGCTGGAGT[AC/GT]AGTGGCATGATCTTG | 84669 |
rs386798147 | in-del | AGTA/GAG | | | intron-variant | USP32 | GRCh38.p7 | 17:60297575 | TGTCTCAGCCTCCCT[AGTA/GAG]GCTGGGATTACAGTC | 84669 |
rs386798148 | multinucleotide-polymorphism | CCT/TCG | | | intron-variant | USP32 | GRCh38.p7 | 17:60339854 | AAAATCCCAAAAATA[CCT/TCG]TTCCTTGCTCTTAAA | 84669 |
rs386798149 | multinucleotide-polymorphism | AAAAGAATGCAT/TAAAGAATGCAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60365720 | AACAAAGTAATTATT[AAAAGAATGCAT/TAAAGAATGCAA]TAAGATAAACCATTT | 84669 |
rs386798150 | multinucleotide-polymorphism | CA/GG | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60379125 | TAATCCTATTGCAGT[CA/GG]AAATCATAATTTAGT | 84669 |
rs386798151 | multinucleotide-polymorphism | ACAGGAATTTATTTATCAGCTTCAAA/TCAGGAATTTATTTATCAGCTTCAAG | | | intron-variant | USP32 | GRCh38.p7 | 17:60382861 | CCCCATACTAATCTC[lengthTooLong]TATTTGAACTAAACA | 84669 |
rs386798152 | multinucleotide-polymorphism | AA/GC | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413176 | AGGAGTTGGAGAGAT[AA/GC]TCATGACTTATGTGC | 84669 |
rs397691577 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60277900 | TGACTATTAAAAAAA[-/A]TAACTTAATAATAGT | 84669 |
rs397707092 | in-del | -/CTTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60192000 | GAACTGGCAAACTTA[-/CTTA]TATTTAACGAGAGGC | 84669 |
rs397749468 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60248176 | CTTTTTTGGTTTTTT[-/T]CCTTATATCACTTTC | 84669 |
rs397784557 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60381456 | AAAAAAAAAAAAAAA[-/A]GGTTTTTATCTGTCC | 84669 |
rs397822657 | in-del | -/A | 0.375 | 0.216506 | intron-variant | USP32 | GRCh38.p7 | 17:60314153 | GAAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs397833209 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60381176 | aggcactgtagccca[C/T]acctgtaatcccagc | 84669 |
rs397833463 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60220746 | tgaggcgggagaatg[A/G]caagaacccgggagg | 84669 |
rs397840035 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60222364 | GTAACAGAAGACCCC[-/C]ATCTATGACTGCTCC | 84669 |
rs397841934 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60381204 | agcactttgagaggt[C/T]aaggccagaagattg | 84669 |
rs397843092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381270 | aacagtgagattccc[A/G]tcactacaacaaaat | 84669 |
rs397843093 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60381272 | cagtgagattcccgt[C/T]actacaacaaaataa | 84669 |
rs397857608 | in-del | -/A | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60210844 | ACATATACAGTAGTA[-/A]TTTTGCATATATTTA | 84669 |
rs397857722 | in-del | -/A | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406157 | GCAAGACCTTGTCTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs397857762 | in-del | -/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60204972 | TTTTTTTTTTTTTTT[-/T]AGAAGAGACGAGGTC | 84669 |
rs397938844 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60351451 | CTTCTTTTTTTTTTT[-/T]CGAGATGGAGTCTCA | 84669 |
rs397955624 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60329492 | TTATTTTTTTTTTTT[-/T]GAGATGAGGTCTCAC | 84669 |
rs397975379 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227072 | AAATCATATTTTTTT[-/T]CTTTCACCAAACATT | 84669 |
rs398031242 | in-del | -/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60225970 | CTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 84669 |
rs398031243 | in-del | -/C | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60273939 | AGTCTCGCTCTGTTG[-/C]CCCCAGGCTGGAGTG | 84669 |
rs398031244 | in-del | -/A | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60314204 | CAGTGAGCCAAGATC[-/A]ATGCCACTGTATTCT | 84669 |
rs398041778 | in-del | -/A | 0.5 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60184331 | AAAAAAAAAAAAAAA[-/A]GTCTCCCCCTCCTCC | 84669 |
rs398079081 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60273938 | GCACTCCAGCCTGGG[-/G]GCAACAGAGCGAGAC | 84669 |
rs398119928 | in-del | -/ATTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60236529 | TTAATTAATTAATTA[-/ATTA]CATTTTTTGCAGAAT | 84669 |
rs527257132 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60376192 | CTGAGATTACAAATG[C/T]GAGCCACTGAGCCCA | 84669 |
rs527264229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60208844 | CTAGCAATAAAAAAG[A/G]TGAGAATTTTCTCTC | 84669 |
rs527270365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317747 | CTTGGGCCTGGGAGA[C/T]TGAGGTACCACTGCA | 84669 |
rs527274658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60217198 | ACCAACAAATCTAGT[A/G]GAATTTATAGAAGCA | 84669 |
rs527314859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326596 | GAGCCACTGTGCCCG[A/G]CCATGGTTTATTTTC | 84669 |
rs527327241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60216334 | CTGGTTAACTACTCC[A/G]CCAAAAATCTAGACA | 84669 |
rs527336355 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60222881 | GAGACGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 84669 |
rs527352238 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256814 | TTGAATTCATACTTA[C/T]AGGTGAATTCTGGAT | 84669 |
rs527353443 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395451 | CAGATTAAAACCTGC[A/G]TTTTGGTTTGTATTA | 84669 |
rs527360017 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60334303 | CATAAGGTTTGATAA[A/C]TTTTAACTTTTAATA | 84669 |
rs527368454 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60317301 | CAAGGATCACTTGAG[C/T]CCAGGAGTTTGAGAC | 84669 |
rs527381221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60333714 | AGGAGAGGGGAGGGG[A/G]AAGAAGAGGAGAGGG | 84669 |
rs527381973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60276587 | GTTCTTATTTCTATA[C/T]TTCTCAGTATTGAGA | 84669 |
rs527383127 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60347159 | AACTTGAAGCTAGAC[C/T]GAGAGTAGAAGCAGT | 84669 |
rs527390709 | in-del | -/TTGT | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60247661 | TGTGGGGGGTTTTGC[-/TTGT]TTGTTTGTTTTGGTT | 84669 |
rs527440288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60185209 | GTGGCAGTTCTCACA[C/T]TGCACTGAATTGCAG | 84669 |
rs527446601 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182911 | TATATCAGGCACTGT[G/T]TGAAGTGCTTTACTC | 84669 |
rs527512636 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60192581 | CTGGGATTACAGGCA[C/T]GCATCACCACGCCCC | 84669 |
rs527513153 | in-del | -/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392974 | TGTGGTAAAATATAC[-/G]TAACAAAATGTACCA | 84669 |
rs527518859 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60370764 | GAAATGCTACTGTCT[A/C]AAAAAAAAAAAAAAA | 84669 |
rs527519411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60341731 | ATCACGAAGTTCTCG[C/T]GCCATGGTTTTCAGC | 84669 |
rs527537427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406426 | TCAAGTGATCCACCC[A/T]CCTCAGCCTCCTAAA | 84669 |
rs527548525 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60399215 | CTGAAGATACAGAAT[A/T]GAGCAAAGTAAAAGC | 84669 |
rs527569402 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60340920 | ATTTTATTTCTCCTT[A/C]ACTTATGAAGCTCAG | 84669 |
rs527582157 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60244678 | GCTCTGTCGCCCAGG[C/G]TGGAGAGCAGGCGTT | 84669 |
rs527588960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60243742 | GTCTGCTGACTAACT[A/G]CTGGCCTAGTATATG | 84669 |
rs527616045 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60222918 | AACTCCTAACCTCAG[A/G]TGATCTGCCCACCTC | 84669 |
rs527617451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192165 | GTACAGTGGTGTGCA[C/T]CTGTAGTCCCGGCTA | 84669 |
rs527619374 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60291553 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 84669 |
rs527630573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358210 | CTGTAAGCCACCACC[C/T]TATGAACCTAATCAT | 84669 |
rs527679827 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60199619 | TTAGCTAGTTTCTAA[C/G]TAAAAAGACCCTTTA | 84669 |
rs527680345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405780 | AACATAAAATAAAAT[A/T]AAATAAATAAATAAA | 84669 |
rs527680414 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413527 | TTTTGATTTCTAATT[A/G]GTTAAGAGGCAAAGC | 84669 |
rs527683638 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60313530 | ACAACATACAAATGC[-/A]AAAGTATAAATTCCT | 84669 |
rs527692013 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60198943 | ATGTAGGGAGACCCT[A/G]TCTCTATAAAGAAAT | 84669 |
rs527732036 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60248207 | TCATATCACTGCACA[A/C]TGAGCTCTATTGTTT | 84669 |
rs527732616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316111 | AGGAGGCAAATGATG[G/T]TTGGCCTTTTTGAAG | 84669 |
rs527749048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60206815 | GGTATATTAGCTAAC[A/G]ACTACCTATCTAACT | 84669 |
rs527752584 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421303 | ACATGCTGGCATAGA[A/G]GACAAGTTAAAAAGT | 84669 |
rs527763989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259972 | TATGGTAAAATTAGT[C/T]TTGTTCTATACCCTT | 84669 |
rs527782707 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231783 | TAATGTAATAATGAT[A/G]GAAAAGATTTCACCA | 84669 |
rs527783943 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60365807 | AATGCCCAGAACAAA[G/T]ATATAAGAGAAAAAC | 84669 |
rs527786473 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420287 | GTGTGAGCCACCGCA[C/T]CCGGCAGAATTATGT | 84669 |
rs527808201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60365252 | TTGGGAGGCCGAGGC[A/G]GGTGGATCATGAGGT | 84669 |
rs527820322 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60192537 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 84669 |
rs527822999 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233089 | AGCAAGTGCAAGGGA[C/G]AAGAGTCCAAGCTCA | 84669 |
rs527823142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60374216 | AGACATAAACACACA[C/T]CTTAGCCTAGGCCTA | 84669 |
rs527827866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267058 | CCTCCCAAAGTGGTA[C/T]GATTACAGGCATGAT | 84669 |
rs527838442 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264784 | AAAATCACTTGAAGC[C/T]GGGAGGCAGAGGTGG | 84669 |
rs527840604 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | USP32 | GRCh38.p7 | 17:60266499 | CTTGTTCTTCTTTTT[G/T]TTTGTTGGAGATGGA | 84669 |
rs527857092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373535 | TGCAACCTGCACCTC[C/G]TGGGTTCAAGCAATT | 84669 |
rs527859109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60382578 | ACCAAGAAAAAAAAA[G/T]TTAATCATAAAATTT | 84669 |
rs527866081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214559 | AGCAAATTTCTTTTA[C/T]TATTTAAAATTAAAC | 84669 |
rs527867827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325098 | GGCAATTTTTAAAAC[A/T]AGGAAAAACAAAATA | 84669 |
rs527871001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315388 | CTCCAGCCTGGGCGA[C/G]AGAGTGAGACTCCAT | 84669 |
rs527936208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60221283 | CTGCAGTCTTAGCTA[C/T]TGGGGAGGCTGAGGT | 84669 |
rs527949323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332214 | GGTGAGCAGAGATCA[C/T]GCCACTCCAGCCTGG | 84669 |
rs527963576 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60328769 | CGCCATCACACTCCC[C/T]GGGAGCAGCCAGAGA | 84669 |
rs527967199 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60292900 | GACAATATATAATCA[C/T]TTCCTACCACTCCCT | 84669 |
rs527984108 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60331341 | GAGGCCAAGGCAGGC[A/G]GACTGCTTGAGTCCA | 84669 |
rs527994127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339597 | TCAAAAAAAAAAAAA[A/C]AAAAAGTATAAACTG | 84669 |
rs527997423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228163 | CTGAGTAGCTGGAAC[C/T]ACAGGCACCTGCCAC | 84669 |
rs527998365 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60244851 | TGGCCAGGCTGGTAT[A/C]GAACTCCTGGCTTCA | 84669 |
rs528003090 | snp | C/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411498 | AGCCTCGGTGACAAA[C/G]TGAGAGTCTGTCACT | 84669 |
rs528039428 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60215891 | CCCAAGTAGAGACAG[G/T]GTCTCTCTATGTTGC | 84669 |
rs528080851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410339 | CAATCAGCATACCCC[A/C]TTCCCTAGTCTCCTG | 84669 |
rs528082498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402788 | GTACGCCATTTAGTG[C/T]CAGCTGCAGTGGCCT | 84669 |
rs528087644 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60203855 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 84669 |
rs528106459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60248521 | CATGTTCCAACTTCT[A/G]TGAAACTCTGTTCAT | 84669 |
rs528118178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409542 | TATTGCAGTAAAAAA[A/T]TACCACAAGCTTAGT | 84669 |
rs528122008 | snp | A/G | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422846 | GATGGGGAAGAGGTC[A/G]CCTCTCATTGTTGGT | 84669 |
rs528128831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312531 | CCCAGGCTCAAGTGA[C/T]CCTCCCAAGAGTCCT | 84669 |
rs528134099 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60226533 | AAATAAAGCTTAAAT[C/T]TTTTTCTTTTCTTCC | 84669 |
rs528143180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60303852 | AGAGATTATCCAAAA[C/T]GAAACAAAAGGGGGA | 84669 |
rs528148395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60203019 | ACCAGAGGTTAGAAG[A/T]GACAAGAAAGCATTC | 84669 |
rs528160122 | snp | A/T | 0.00135243 | 0.0259689 | intron-variant | USP32 | GRCh38.p7 | 17:60212001 | TAAAATAATCTCTTT[A/T]AAAAATAATACTGGA | 84669 |
rs528185381 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60247688 | TTTGGTTTTTTTTTT[G/T]TTTGTTTGTTTTTGA | 84669 |
rs528190001 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416498 | GCACATATTTGGATT[A/T]AAAAAAATGTGGTGG | 84669 |
rs528191132 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60256836 | ATTCTGGATTGGGCC[A/C]GTCAACATTAATCAA | 84669 |
rs528194858 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60283083 | AACTCAAAGAGAAAT[A/G]GACAAGCATGACAGA | 84669 |
rs528200144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60370091 | ACTCTTGTTGCCCAG[A/G]CTGGATTGCAATGGC | 84669 |
rs528201705 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60256186 | CTTTGAAAAAAAAAA[A/T]AATAAAAATAAAGAA | 84669 |
rs528203713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60264063 | ATAGTAATGCAAGCT[A/G]TAGGAGTAAATCTAT | 84669 |
rs528215715 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60211630 | ATCAGCTAAATGGTG[C/T]TAATAATTCTCTAGC | 84669 |
rs528254704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369156 | CCCGCCACTACGCCC[A/G]GCTAATTTTTTGTAT | 84669 |
rs528256553 | snp | A/C/G | 0.000168026 | 0.00916443 | intron-variant | USP32 | GRCh38.p7 | 17:60211350 | AAAGTCACAGGTTAA[A/C/G]AGGCCAGTGACTCCA | 84669 |
rs528258056 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60280019 | GATAAGGTAATAATA[A/G]TTTGGAATTTACACT | 84669 |
rs528258140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378907 | TAAAATAGTTCAAAT[A/G]GTAAATGGTATGTTC | 84669 |
rs528265090 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60325341 | GAGAATCTCTTGAAC[A/C]TGGGAGGCAGAGGTT | 84669 |
rs528266011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263362 | ATCATTAAATAGTCA[A/G]CAGATGAATTAGATA | 84669 |
rs528298708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378256 | ATACTATGTCACACC[A/C]ATTAGGATGGTTATT | 84669 |
rs528342085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60328169 | GTGCCTTTTCCAGGC[A/G]CAGCAATCCATAGAC | 84669 |
rs528360417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60344934 | CTCCTGAGTAGCTGG[A/G]ACTACAGGGACGCAC | 84669 |
rs528370368 | in-del | -/AGAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60401380 | GTCTCAATTAAAAAG[-/AGAA]AGAAAGAAAGAATTA | 84669 |
rs528373674 | snp | A/G | 3.29592e-05 | 0.00405938 | synonymous-codon, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179402 | AATGTAGGCAGAGTC[A/G]GTGTCAATTTCATCC | 84669 |
rs528378821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60336438 | AGAAATGAATTGGCC[A/G]GGCGCGGTGGCTCAC | 84669 |
rs528380629 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60307993 | AGAACGATGCGGAGT[C/T]AGGGTGGGGCAGTCA | 84669 |
rs528430194 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60288310 | CCAGGCATGGTGGCG[A/T]GTGCCTGTAGTCCCA | 84669 |
rs528436178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60269362 | TTATAAAAATTCAAG[A/C]CTTAATCCACAGATA | 84669 |
rs528447244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60278405 | TCTGGGAGCACATAC[A/G]TGGGTAGGCCCTGGA | 84669 |
rs528458005 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178526 | GGTAGCTGGATTTCC[C/T]AGGATGCTGTTTCTT | 84669 |
rs528494108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401851 | TTAACAAACAAATCA[A/C]TTCATGCAAAAATCT | 84669 |
rs528498310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186889 | CCTTCTGTTTGTCCC[C/T]CTAATGTATGGGAAG | 84669 |
rs528529395 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60285756 | TTTCATGAAAAAGAG[A/G]GTATGTGATTTAAGT | 84669 |
rs528535530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60344556 | CTGGACTCAAGCAAT[C/T]CTCCTACTTCAGCCT | 84669 |
rs528571060 | in-del | -/T | 0.323434 | 0.238972 | intron-variant | USP32 | GRCh38.p7 | 17:60277918 | CTTAATAATAGTTCC[-/T]TTTTTTTTTTTTTTT | 84669 |
rs528573661 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60343811 | CCAAGGCGGGTAGGT[C/G]ACCTGCGGTCAGGAG | 84669 |
rs528598216 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60294195 | ACAGGTGTGAGCCAC[C/T]TTGCCTGGCCCAAAG | 84669 |
rs528610948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60352259 | AACAGCTGGCAAATA[C/T]CCTTTTGCCCTTATC | 84669 |
rs528615975 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242305 | GCTCCTCCTGGACCA[-/T]TTTTTTTTCTTTTTA | 84669 |
rs528617377 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305826 | CTTTCAGTTTTGCAA[A/G]TACTTGTAAAATGTA | 84669 |
rs528617723 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60360354 | TTACAAATACAAAAA[-/TT]ATTTTTGTATTTGTA | 84669 |
rs528620809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186029 | CTGCGCTCCAGCCTG[A/G]ATGACAGAGAGAGAC | 84669 |
rs528629237 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60360585 | AATTGCTTGAGCCTG[A/G]AGGTGGAGGTTGCAG | 84669 |
rs528658980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60293315 | AAAAAATATCATACT[A/T]CCTGAAAAAGAAAAG | 84669 |
rs528686762 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407608 | AGACTACAAAATACA[A/G]ACATTCAACAATGTG | 84669 |
rs528691751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60201727 | GCAATGGCATGATCT[C/T]GGCCCATTGCAACCT | 84669 |
rs528692525 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60310488 | GGCAGATCATGAGGC[A/G]AAGAGATTAAGACCT | 84669 |
rs528701257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301950 | ATTTTTCAACTTTAC[A/G]ATGGTGTGAAAGTGA | 84669 |
rs528708051 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60201271 | AATGTTCCATTATCT[C/T]AATATATCTCAGCTT | 84669 |
rs528715830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60245579 | ATATCAGTGTAACTG[A/G]TGCTGGATGAAATTC | 84669 |
rs528719134 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60354380 | GTTTGGTTCCAAAGG[C/T]AAAGAGGAAAATTTA | 84669 |
rs528738121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60309925 | GGCATGTGCCTGTAA[G/T]CCAAGCTAGTCGGAA | 84669 |
rs528745599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423488 | GTGAGCCACTGTGCC[A/C]AGTTTTGCTCTGTCA | 84669 |
rs528768375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261981 | AGCCCATTTGCTATA[C/T]TGACACCTGAGTAAT | 84669 |
rs528769589 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60209666 | ACTTAGTCTGCCTCT[A/G]TTTCAACAAATATAT | 84669 |
rs528784469 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60386948 | ACTACTTAAAAACTG[-/C]CCCATTTTTCTCCTT | 84669 |
rs528785104 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60351716 | TACAGGCGTGAGCCA[-/C]CAAGCCCAGCTGTCA | 84669 |
rs528799200 | snp | A/C | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178223 | TTTGTAATTTATAGC[A/C]CTTAGAGCCATCAAA | 84669 |
rs528807545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60367069 | CCTGACCTTGTGATC[C/T]GCCCCCCTTGGCCTC | 84669 |
rs528813296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60361450 | AGGTATTCACTTACT[A/G]TTCATATTTAGGCTG | 84669 |
rs528855988 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178759 | TGCCTTAAGAATCAT[C/T]TGCACACCTTCGTGA | 84669 |
rs528860643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211251 | ATTCCTTGGCCTATT[A/T]CATATTAAATAGGGC | 84669 |
rs528873341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60202914 | ATTCAATAAGTATCC[G/T]TATCAGAGAAAGACA | 84669 |
rs528888571 | snp | C/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420976 | TCCAAATTGTCACTA[C/T]TGTAACAGTCCTCAT | 84669 |
rs528924591 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60387615 | AACTATAAACAGAAT[G/T]TCTAGTATTTTATTC | 84669 |
rs528928934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416423 | CAACCTGCATAAAGA[A/G]GGGGGTGGGCAAATT | 84669 |
rs528934442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60310646 | GGAGGTTGCAGTGAG[C/T]CAAGATCGACCCACT | 84669 |
rs528946349 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360763 | GGTTGTTGTGCTGGG[A/T]TTAATTTTTTAAATT | 84669 |
rs528955810 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60319548 | TCTGGGAGGCTGAGG[C/T]GGGCAGATTGCTTGA | 84669 |
rs528966213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424446 | AATGATATTGAAACC[A/G]TCCCTAGAAACTTTA | 84669 |
rs528980359 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60216678 | TTGTAACTGTAAGAA[A/G]GTTTGAATACTTGTC | 84669 |
rs529003968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423667 | AATTGGGTTTTGCCA[A/T]GCTGGCCAGGCTGGT | 84669 |
rs529015012 | snp | A/G | 0.000244156 | 0.0110462 | intron-variant | USP32 | GRCh38.p7 | 17:60219602 | TTAAGGAAATGCATG[A/G]TATTCTTGCTGCATT | 84669 |
rs529037020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60270153 | AATCCTGTGGTTTTC[A/C]AACATTTCGTAAAAA | 84669 |
rs529041532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60262604 | AGGTTTCTCCATAGT[C/T]TGGTATAAAGTTCAA | 84669 |
rs529044380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327988 | TGCTGGCCTGCAGGT[G/T]CCCCTTGGCAGGAGC | 84669 |
rs529049946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60269254 | AGCAAATATCCCAAA[C/G]TATTCCATAGTAAAA | 84669 |
rs529080381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327249 | ACACTGATGGCAACG[A/G]CGAGCCTTCTGGAGT | 84669 |
rs529091961 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60278317 | TGAACAAGACAATTA[A/T]GTTTAGAGATGAGAA | 84669 |
rs529100208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60217356 | AATAGAGTGCATGGC[A/G]CGATCTCGGCTCACT | 84669 |
rs529115297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268579 | CAGAACAAGACCCTG[C/T]CTCAAAAAAAAAAAA | 84669 |
rs529118233 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60326743 | AAAATTCATGCACAG[A/G]GTATAAAATATTCCC | 84669 |
rs529118608 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60335210 | AACTCCTGGGCTCAA[A/G]CAATCCTTGAGATTC | 84669 |
rs529137426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308499 | CACAGACCAATGGAC[A/G]ACAGAGAACCCAGAT | 84669 |
rs529178776 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60343585 | GAAGGCAGAAATAAA[A/G]ATGTTCTTTGAAACC | 84669 |
rs529191809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186793 | AAGGAAGGATCTAGA[A/G]TGCAACAGAAAAGAA | 84669 |
rs529203988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185966 | AGCTACTCAGGAGGA[C/T]TGCTTGAGCCTGGGA | 84669 |
rs529203989 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60260591 | AGAGGATAAAAAGAC[C/T]AAGTTAATCTATATA | 84669 |
rs529207387 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60223818 | ATGAACATTTGGCCA[C/T]CCTCCTAGAATATCT | 84669 |
rs529211971 | snp | C/T | 0.00031958 | 0.0126368 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231565 | TCGTGGCAGTCCTGA[C/T]GACGATCCTCGAGGG | 84669 |
rs529212223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60277155 | TTTATCACCCACCTA[C/T]AGGTATAATTTTTTC | 84669 |
rs529220783 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283245 | CATGGTGTGGTCACG[G/T]TATATTGACCAGTGC | 84669 |
rs529239914 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60294130 | AGGCTGGTCTTGAAC[G/T]CCTGGGCTCAAGAGA | 84669 |
rs529252407 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60293232 | AAGTTTTTAGAGTAC[C/T]GGGTAGCCAACCACC | 84669 |
rs529253955 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393316 | CTCTCCATTTCCCAA[A/C]GAATGAAAAGCAGGG | 84669 |
rs529253991 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60384788 | CAAGAGCAAAACTCC[A/G]TCCAAAAAAAAAAAA | 84669 |
rs529267472 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60185390 | AAAAATAACAAAACC[C/T]CCTGTTTGTTCATGT | 84669 |
rs529309002 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60338342 | AAAAAAAAAAAAAAA[C/T]ACTACATAGAAATGT | 84669 |
rs529309461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301827 | GGTAAATTTTAGTGA[A/T]ATCATGTTAAGTTTC | 84669 |
rs529370280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60351616 | TATTTTTAGTAGAGG[C/T]GGGGTTTCGCCATGC | 84669 |
rs529377883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192682 | CACCCACCTCGGCTT[C/G]CCAAAGTGATGGGAA | 84669 |
rs529395244 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | USP32 | GRCh38.p7 | 17:60245463 | GACCAGGAAATTCTG[A/G]AAGCCACTGGGCAGC | 84669 |
rs529399797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60201220 | ATTCATTTATACTCT[A/G]TATAACTACAAATCC | 84669 |
rs529403758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237376 | GGTCTTGAACTCCCA[A/G]AAGTGTTGGGATTAC | 84669 |
rs529404981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60292197 | CTTTTCTTGCAGGCT[A/G]TTTCTTAGTGGTCTG | 84669 |
rs529423096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301076 | GATATATCATGTTTT[A/G]TTTATCCATTTACCA | 84669 |
rs529424600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360077 | GTTTCACCATGTTAG[C/T]CAGGATGGTCTTGAT | 84669 |
rs529454377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60253658 | GTAATCCCAGCTACT[C/T]GGGAGGTTGAGGCAG | 84669 |
rs529462647 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406602 | CTCACTGTAATCTCC[A/G]CCTCCCAGGTTCAAG | 84669 |
rs529467906 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60367047 | TTAGCCAGGATGGTC[C/T]CAATCTCCTGACCTT | 84669 |
rs529477694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422825 | GACCTGTGTTCCTGG[C/T]GAGATGATGGGGAAG | 84669 |
rs529481210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200418 | ATACAAAATTAGCCA[A/G]GCGTGGTGCCGCATG | 84669 |
rs529501930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60209599 | ATAAAATTTGGAATG[A/G]ACATGTCCTATAATC | 84669 |
rs529525928 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60207828 | CATATAGGCAGCCTT[A/T]CGTATTTCCCTTCTT | 84669 |
rs529572100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316239 | TGCTATGATGAGTAA[C/T]ATTTCATTCTCAAAA | 84669 |
rs529576755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216006 | GTGTGTGAGCTACCA[C/T]ATTTGGTCAAAACAG | 84669 |
rs529578640 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60355382 | TTTGTATTTTAGGAT[A/G]TAAAAATTTTCCCTC | 84669 |
rs529608188 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60366716 | GACCATCCTGGGAAA[A/C]ACAGCAAGACATCGT | 84669 |
rs529626342 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60375454 | GTACTTAAAGGAACG[C/T]CTACAATGCACCATA | 84669 |
rs529690931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60389176 | AGTAGATGAAACCAA[C/T]GAATGCAGGTTTTAC | 84669 |
rs529712846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190436 | ATATATTAGGTGCCA[C/T]AGAGGATGCCAATGA | 84669 |
rs529714581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404660 | GAAATTGTAGAAGAG[C/T]GCACCTCAGCCTCCT | 84669 |
rs529720572 | in-del | -/TTG | | | intron-variant | USP32 | GRCh38.p7 | 17:60253383 | ACACTCAACATGTGA[-/TTG]TTATTTTAAAAAGTA | 84669 |
rs529729370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60347575 | AGCCAGGATGGTCTC[A/G]ATCTCCTAACCTCGT | 84669 |
rs529750018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234850 | TCAAAGTCCCGAGAT[G/T]ACAGGCCCAGCCAGA | 84669 |
rs529754838 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60201015 | CAGGTGTGTGGCACA[C/T]GCTGGCTAATTTCTG | 84669 |
rs529758117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348061 | CGGGAGGCGGAGCTC[A/G]CAGTGAGCCAAGATA | 84669 |
rs529782900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60267681 | GTCCACCACCACGCC[C/T]GGCTAACTTTTGTAT | 84669 |
rs529783184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60189952 | GCTATAGTTTGGACA[C/T]GGTTTATTTGTCTCC | 84669 |
rs529816193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249561 | ATTTTATTATCCTTG[A/G]ACAGGCATTTATTCC | 84669 |
rs529817737 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60241161 | CGCCACCATGGCCGG[C/T]TAATTTTTTGTATTT | 84669 |
rs529829554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356466 | GTTGCAAACTGACTG[C/T]ACAACATTTGAACAC | 84669 |
rs529838882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297540 | TGCAACCTCCACCTC[C/T]TGGATTCAAGCAATT | 84669 |
rs529846046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197277 | TTTTTAGTTACCATA[A/C]AACAGAACTCTCATT | 84669 |
rs529864787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258152 | GAAGTTGAGCTCCAA[C/T]GGTGCCATGAAATGA | 84669 |
rs529868579 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60419002 | CATTCAACCCAGCAA[A/T]CCTGTTACTGGATAT | 84669 |
rs529896902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60313546 | AAAGTATAAATTCCT[G/T]AAGTCTAAGCAAAGA | 84669 |
rs529912350 | snp | C/G/T | 4.94395e-05 | 0.00497169 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205552 | CTTCTCAGTTCCACA[C/G/T]GGCACAACAGTGTTT | 84669 |
rs529913885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60314589 | AGGAGAGAAAATAAT[A/C]AGTCTCAGTAACCTG | 84669 |
rs529922932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204868 | AGCTTTGACCTCCTA[C/G]TCTCAAGTGATCCTC | 84669 |
rs529946246 | in-del | -/TA | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60357035 | GAGGTTGCAGTGAAC[-/TA]TATGATTGCATCACT | 84669 |
rs529979472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264735 | CATGGTGGCACACAC[C/T]TGCAGTCCCAGCTAC | 84669 |
rs529984328 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60370337 | GGTTCTACTTTGACA[C/G]CAATCCAAAAAAAAC | 84669 |
rs529998887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60372340 | GTGATTTCATCATTG[C/T]GCAGACATCAGCGTG | 84669 |
rs530006371 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60363307 | TAAAATACAAAAAAT[C/T]AGCTGGGCGTAGCGG | 84669 |
rs530015662 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60380334 | CACTTTGGGAGGCTG[C/T]GGTGGGTGGATCTCT | 84669 |
rs530022797 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373789 | ATAAACTTTTAAATT[C/T]AACTTGTTGGCTCTT | 84669 |
rs530048348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387968 | GTAAAGTTAAATTGT[A/T]AGTCGGGGATTGTCT | 84669 |
rs530050558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271232 | TTTCCCCACTCCATT[A/C]AACCTGCAAACATAT | 84669 |
rs530083554 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60350512 | CAGGCTGGTCTCAAA[C/T]TCCTGACCTCAAGTG | 84669 |
rs530089708 | snp | A/C/G | 0.000164371 | 0.00906441 | intron-variant | USP32 | GRCh38.p7 | 17:60219599 | TTTTTAAGGAAATGC[A/C/G]TGGTATTCTTGCTGC | 84669 |
rs530090454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60220329 | CCACATTTCGTTAAT[A/G]TGAAGAGTATTATAA | 84669 |
rs530096806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312820 | TTCACAAAATAAGTC[A/T]TGCTGTATGTTGGTG | 84669 |
rs530097583 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60348268 | CATCAGTATAGAGGT[-/A]AGTAATTAAAACCAT | 84669 |
rs530098549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381756 | CTATTACTTACGTAA[A/T]CTGTACAAATCTTAC | 84669 |
rs530103600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212195 | CTTATTCCTAAATCA[G/T]AAGTTTTAAAATCTA | 84669 |
rs530133469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228127 | GCCTCTAGCTTCAAA[A/T]GATTCTCCTGCCTCA | 84669 |
rs530141989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337633 | TGTAATCTCAGCTCT[C/T]TGGGAGGCTGATGAG | 84669 |
rs530143276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60329925 | AGAGATACTCAGAGC[A/G]TAAGCAGTATTACTA | 84669 |
rs530150927 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60310561 | AAAATTAGCTGGGCG[C/T]GGTGGCACGCGCCTA | 84669 |
rs530158731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60226825 | GCACTTTGGGAGACC[A/G]AGGCAGATGGATCAC | 84669 |
rs530179527 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60387561 | CATATATACTACTTT[C/T]GAACATATTATGTGC | 84669 |
rs530211869 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60253173 | AGGAAAGGCAATACC[-/AA]AAGTCAAAATGCTAT | 84669 |
rs530217925 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60345873 | TATAATCCCAGCTAC[A/T]TGGGAGGCTGAGACA | 84669 |
rs530219743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60287983 | GCCAGGCATGGTGGT[A/G]GGCGCCTGTAGTCCC | 84669 |
rs530252770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60394231 | TCAGCCTGCAGAGTG[C/T]GAGTTCCGAGTTAGA | 84669 |
rs530257211 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60240111 | TAAGATAATTGATTT[C/T]AAATGTTTGTCTACT | 84669 |
rs530261785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60395602 | TCGTTTAGTTTGTTC[A/C]ATTTCATTATAATTA | 84669 |
rs530262400 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60245083 | CACTCATATAAGATC[A/G]TTATATGTAATGGGA | 84669 |
rs530267329 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60254311 | TAGCTTTCCTTCTTT[C/T]CTTCCCACTTAATCT | 84669 |
rs530274666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60345319 | CTTGACCTCTAAGAA[C/T]ACAGCCACGTTGACA | 84669 |
rs530289230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409409 | GCCTCTATGCACGTC[A/G]GGCAGTGAGCCCATT | 84669 |
rs530304932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60279408 | GAGGATCCCTTGAGC[C/T]TGGGAGGTTGAGGCG | 84669 |
rs530318453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296421 | TGTAAGAAAGGCAGG[A/G]ATTAGAACGATATAG | 84669 |
rs530330362 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60247678 | GTTTGTTTGTTTTGG[G/T]TTTTTTTTTGTTTGT | 84669 |
rs530356556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60195664 | TGATGCTTCTTTTTC[C/T]CTTTTCAATCTCTAA | 84669 |
rs530361682 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60336585 | GCCGGGCGTAGTGGC[A/G]GGCGCCTGTAGTCCC | 84669 |
rs530380595 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295358 | AAATATCAAAAGATA[C/T]AATATTCAGAGGAAA | 84669 |
rs530393649 | in-del | -/TT | | | intron-variant | USP32 | GRCh38.p7 | 17:60245137 | TCATGTAAAAATGTC[-/TT]TTAAACCAGTAAAAA | 84669 |
rs530400538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60344706 | GTGATCCTCCTGCCT[C/T]GATCTCCCAAAGTGC | 84669 |
rs530410860 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60248403 | TCTAAGATTAATAAT[C/T]TTCGAGAAATTTTAG | 84669 |
rs530416232 | snp | A/G | 1.77212e-05 | 0.00297663 | synonymous-codon, intron-variant | USP32 | GRCh38.p7 | 17:60288680 | ATAGTTTACCTTTTC[A/G]CCCTAAAATTAAAAC | 84669 |
rs530428497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297516 | TGCAGTGGCGCAATC[C/T]CGGCTCACTGCAACC | 84669 |
rs530437936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197121 | GGAGGTGGAGTTTGC[A/G]GTGAACAAAAATCAC | 84669 |
rs530459929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60205825 | ATTTTAATTTTCCAG[C/T]TTTACTTCCCTAACT | 84669 |
rs530484401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410395 | CTAGCCTCGGTGGGC[A/G]CGGTGGCTCATGCCT | 84669 |
rs530516260 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60355364 | ATGCAAGGACACATG[A/C]CTTTTGTATTTTAGG | 84669 |
rs530538356 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP32 | GRCh38.p7 | 17:60195493 | CAGGCACGTACCACC[A/G]TGCCCGGCTAATTTT | 84669 |
rs530538686 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60274696 | AATTCAAAGTACAGA[-/T]TTTTTTTTTTTGACA | 84669 |
rs530569721 | in-del | -/AC | | | intron-variant | USP32 | GRCh38.p7 | 17:60386018 | TTCTATTGCTGCATA[-/AC]ACACACACACACACA | 84669 |
rs530592369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256928 | AACACTGACCAACAA[C/T]GTGATTTCATCATTC | 84669 |
rs530594339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60296835 | CTAAAAAAGAAAATC[C/T]TAAGCACCCCAACCA | 84669 |
rs530607345 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60203934 | CAATCAGCTATCTAG[C/T]GGCAGAATTAGAACT | 84669 |
rs530609085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60276096 | TTTTAAAATATATAA[C/T]GGCTGGGCGTGGTGG | 84669 |
rs530614820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60313425 | GTGTTTCATAATACT[A/T]ACCATGTCTTTCCTG | 84669 |
rs530617549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418250 | GGCGTGAGACCCCTC[A/G]CCTGGCTAATTTTTG | 84669 |
rs530620461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60249352 | TCCTGAGTTTGTGTA[C/T]AGCCTTGTACAAGCA | 84669 |
rs530623785 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60277329 | AAAAAGGCCAGGCAC[A/G]TATCCAAATATTTTC | 84669 |
rs530634877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60248641 | TGCTAGAATTTCTAT[A/T]TGATTCTGTTTTAAA | 84669 |
rs530650661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312608 | ATCACACCTTGCTAA[C/T]TTTTTCATTTTTTTG | 84669 |
rs530653752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363252 | CTGAGCTCAGGAGTT[C/T]GCAACCAGCCTAGGC | 84669 |
rs530655044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204760 | AGATGTGAGCCACCG[A/C]ACCTGGCCATTTTCT | 84669 |
rs530663540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354305 | CTATTTCTTTAAGAC[A/G]GCCAAGGCAGGACCA | 84669 |
rs530731661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409693 | TTGTTCATTTCCCAG[C/G]ATAGGCCAAACTAAC | 84669 |
rs530736697 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305295 | GGGAGCAGAGAACAA[A/G]CATGTCACATGGTGA | 84669 |
rs530755514 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60271135 | ATGAGCATGCTCGGG[G/T]GCAGAGAGCTAAACT | 84669 |
rs530759028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60222774 | GCAGCCTCCGCCTCC[C/T]GGGTTCCAGTGATTC | 84669 |
rs530768426 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60280107 | ATTATTATTATTATT[A/T]TTTTTTGAGATGGAG | 84669 |
rs530788172 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60219560 | GCAACGTAGTTTTCA[A/C]CTTTTTTTTTTTTTT | 84669 |
rs530788498 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | USP32 | GRCh38.p7 | 17:60226499 | TTCTGTTGGCAGCCA[-/T]TTTTTTAACATTAAA | 84669 |
rs530797374 | snp | A/T | 1.66693e-05 | 0.00288693 | missense | USP32 | GRCh38.p7 | 17:60211384 | AGATTACCTGTTGAG[A/T]TCATAAAGATGTCTC | 84669 |
rs530808693 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60338102 | GCTAGGACAGGCAGA[A/T]AGCTTGAGCCCAAAA | 84669 |
rs530821421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60370249 | ACATCTTTAAGAACT[A/G]AAATGATGACAACAA | 84669 |
rs530845615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60319857 | TTTACATTGCAATAG[A/G]TATTATAAATAATCT | 84669 |
rs530846877 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60340775 | AGCATCAATGATCTT[C/G]ACAATTTGGCATGTT | 84669 |
rs530860216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232897 | CTACTACTACCACCA[A/T]TATTACCTTTAACCT | 84669 |
rs530874869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263469 | AGGCTTGGTTAAAAA[A/G]CCCAAGTTCTATCCC | 84669 |
rs530893420 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60351586 | GCACGCACCACCGTG[C/G]CTGGCTAATTCTTGT | 84669 |
rs530904096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378293 | AAGAAAACAAAATAA[C/T]AAGTATTGGGTAGAT | 84669 |
rs530904225 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218877 | GGGATTACAGGCATG[A/T]GCCACTGTGCTCAGC | 84669 |
rs530926722 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60257942 | GTAAGCCCAAGAATA[C/T]AGTCATTGGTTTCTT | 84669 |
rs530931168 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60239609 | GGAGAACCCCTCTAA[C/T]AGATTTCTCATTTCA | 84669 |
rs530939194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60287217 | CGTGAGCCAGTTAAC[A/G]TTCTTTTCTGCTGAC | 84669 |
rs530957476 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394152 | GGAATACATTTCAAA[G/T]CCTTTAATTTCCAGG | 84669 |
rs530967730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225601 | TTCTGTTAATGGAAG[A/C]CTGATCTCCTATTAC | 84669 |
rs530971771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60353206 | CCAAAGGGCTCAAGC[A/G]CAACATAGGCACAGA | 84669 |
rs530983718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60328337 | GGTGCAGAGAGGAGC[C/T]ACCCTCTCTGCTGAG | 84669 |
rs530987916 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283763 | CTAGAAAGTATAACC[A/T]AGAGGCATTTATTAA | 84669 |
rs531004211 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295242 | AGAGCAAAACTTCGA[A/G]AAAAAAAAAAGATAA | 84669 |
rs531009476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60336482 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 84669 |
rs531034632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408787 | AAGCAAGCATGCAAC[A/G]ATAGGGGGAATCTAA | 84669 |
rs531045856 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178749 | TCCTCGTCCATGCCT[G/T]AAGAATCATTTGCAC | 84669 |
rs531049862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232242 | CAGTGGCATGATCTC[A/G]GCTCACTGCAACCTC | 84669 |
rs531053773 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60345968 | GCATGGACAACAGAG[A/C]GAAACTCTGTCTCAA | 84669 |
rs531061237 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60384313 | CTTTTGCCACAGGGA[A/T]AAGATGCTGGGGCAA | 84669 |
rs531073694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416142 | TGCGCCTGGCTTACT[C/T]TTGGGTTTCTTACAA | 84669 |
rs531083445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60343841 | GTTCAAGACCAGCCT[A/G]GCCAACATGGTGAAA | 84669 |
rs531106433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60361332 | CACAGAAACTTACAG[C/T]GGTTAGCATATAATA | 84669 |
rs531118764 | snp | G/T | 1.65162e-05 | 0.00287365 | missense | USP32 | GRCh38.p7 | 17:60255183 | AACATACCTGGAAAA[G/T]GAGGTTCAAAAACTC | 84669 |
rs531128060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286703 | TGTTTGATTTCCCTA[C/T]AGCAACTAAAGATAA | 84669 |
rs531135412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201840 | ATTTTTGTATTTTTA[A/G]TAGAGATGGAGTTTC | 84669 |
rs531139159 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60294323 | GGCTAATGAATGAAT[G/T]ATATCCGTGATGAAA | 84669 |
rs531164743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60275862 | GATTACAGGCACCTG[C/T]CACCATGCCTGGCTA | 84669 |
rs531178502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60374459 | GAAGAGTGCACTGGC[G/T]TGATCAAGGCTCACC | 84669 |
rs531213486 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60391765 | AGGCCGGCCGCCTTT[C/T]CCTTCCGCCTCAGGC | 84669 |
rs531224052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60275282 | GGAAACATGGTGAAA[C/T]GCCATCTCTACTAAA | 84669 |
rs531242286 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60381996 | GTGTGTATGTGTGCA[G/T]GGTGAACTCATTTTT | 84669 |
rs531246877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60230512 | TGCCTCTAGCAACTG[C/T]GGTTCTACCACATGC | 84669 |
rs531247401 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60333435 | GAAACCCCCATCTCT[A/G]CTACAAATACAAAAA | 84669 |
rs531260891 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403020 | GTAAGCCGTATCTCT[G/T]TTTTTTTTTTGAGAC | 84669 |
rs531306870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60383937 | TAAGAATACACTGAC[C/T]GTGTGAAACTAGGAA | 84669 |
rs531310644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60215264 | GGTGTGAGCCACCAA[A/G]CCCAGCCTTCCAGGT | 84669 |
rs531327430 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60328948 | AGCTCCACGCCTGAC[G/T]CACGCAGTCTCCCTT | 84669 |
rs531374071 | snp | A/G | 0.000247074 | 0.011112 | synonymous-codon | USP32 | GRCh38.p7 | 17:60222493 | TTCATAGTCTCTTCC[A/G]TGAATCAGCTGTGGA | 84669 |
rs531380341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60333616 | AAACAAAAAATAAAT[A/G]AATAAAGGTAAGAAA | 84669 |
rs531419028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333105 | CTTCAATTACAGTTG[A/T]CCCTTGAACAACACA | 84669 |
rs531443798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235690 | TAAAATAAAGGACAA[C/T]GTAAATGATGTAGTT | 84669 |
rs531448488 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60363476 | AAAAAAAAAAAAGCG[C/T]CACTGCACTCCAGCC | 84669 |
rs531451231 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60374492 | AGCCTGAACCTCCTA[G/T]GCTCAAGTGATCCTC | 84669 |
rs531485160 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60348168 | GATGATAAACTTTTT[A/T]AAGGATACTGAATAT | 84669 |
rs531488498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192155 | AATTAGCTGGGTACA[C/G]TGGTGTGCACCTGTA | 84669 |
rs531489625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243220 | ATCTTGTATCCTGTC[A/T]TGTTGCTGAACTCAT | 84669 |
rs531497836 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60228111 | GCTCACAGCAACCTC[C/T]GCCTCTAGCTTCAAA | 84669 |
rs531503685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60251645 | AATGAAAGACACTCA[A/G]GTTATTAAAAATTGG | 84669 |
rs531513319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60395952 | ATTGCTACAACGTGA[C/T]ACCAACACATTAAGA | 84669 |
rs531522812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60291465 | AGATAGAAAAAGCTG[A/G]GACCCATATCACTTA | 84669 |
rs531525255 | in-del | -/A | 0.290719 | 0.246662 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404041 | CGAGACCCTGCCTCA[-/A]AAAAAAAAAAAAAGG | 84669 |
rs531537942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60299626 | AAGTTTCCACACATG[A/G]ACTTTGGGTAACGTG | 84669 |
rs531554011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60365203 | GACCATGTTTTAGCC[A/G]GGTGCGGTGGCTCAT | 84669 |
rs531554259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60191524 | TATTATTATTATTTT[A/T]CTTGAGATGGAGCCT | 84669 |
rs531561922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60250611 | GACAATCAAGAAAAC[A/G]CTCAAGAATATCAAG | 84669 |
rs531576445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348755 | CCTGGGTGACAGAGC[A/G]AGACTGTCTTAAAAA | 84669 |
rs531577065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339941 | AAGTTCTTTCCATCT[A/G]CAACTGGCAGCTTGT | 84669 |
rs531592602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412657 | CAGTCTCACCAAATC[C/T]GGGCCTGAAGGGAGG | 84669 |
rs531597975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214460 | AGGTAAAATCCCATA[C/G]TCATGAAATATGATT | 84669 |
rs531602378 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60198180 | GACATAGGCTGGGTC[C/T]TATCAGTCATGTAGA | 84669 |
rs531614574 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | USP32 | GRCh38.p7 | 17:60205783 | AGGGAGAAATCACAG[C/T]ATAAATAATTCTAGA | 84669 |
rs531687560 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405344 | AGTAGCTGGGATTAC[A/G]GGCACACACCTCCAA | 84669 |
rs531689746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258537 | AGCGTGACAAAAGTG[A/C]CTTTGTTGTTGATCC | 84669 |
rs531722748 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60372609 | CTTTGGAAGACTGAG[A/G]TGGGAGAATCACTTG | 84669 |
rs531724094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60323083 | CACTTTGGAAAATAG[C/T]CTGGCAGTTCCTCAA | 84669 |
rs531781229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381102 | AGCTTTCTCCTTTAA[A/G]GAGAAAGCACAGCAG | 84669 |
rs531787143 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60374055 | TGGGTGTGGTGGCAT[A/G]CACCTGTAATCCCAG | 84669 |
rs531807229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60323861 | AAAGCGTCAAAACAT[C/G]TCTACAGCTTCTGCC | 84669 |
rs531809270 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60266487 | GCAGAGTTGTTTCTT[G/T]TTCTTCTTTTTGTTT | 84669 |
rs531810669 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419280 | AGAAAACCAAATACC[A/G]CATGTTCTCACTTAT | 84669 |
rs531819148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388933 | TTCCAAGGCCCCGCT[C/T]TGCAAGATAAACTGC | 84669 |
rs531827236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60220490 | GATGTAAAAAAAACT[C/T]AGATTTCACATTGTT | 84669 |
rs531834241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60331276 | TACAATAAAACTGCA[C/T]ATACTTAGACTGGGT | 84669 |
rs531861525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227192 | CAGAGTCTTCAAAAG[A/G]CAACACTATTAGCTG | 84669 |
rs531903085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60338327 | AAGACTCTATCTCAA[A/G]AAAAAAAAAAAAAAT | 84669 |
rs531940956 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60304603 | AATGTAAAGTGTCTT[C/T]ATAGAATATGTAAAA | 84669 |
rs531951542 | snp | A/G | 1.8572e-05 | 0.00304724 | intron-variant | USP32 | GRCh38.p7 | 17:60181760 | GAACCTGTGAACAGG[A/G]CAGAAGAAAAGATTC | 84669 |
rs531960509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60272389 | ATATACATCAAAAAT[C/T]GCAAATAGGCTCTAA | 84669 |
rs531970065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274375 | GGCAGAAAAATATCT[A/C]AAAAAATAATGGCTG | 84669 |
rs531982845 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60234774 | TAGAGATGGAGTCTC[A/C]CTATGTTGCCCAGGC | 84669 |
rs531993016 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60398981 | GTGAGACTGTCTTTA[A/C]AAAATAAAATAATAA | 84669 |
rs532001182 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60282809 | TCTGGAGGCAATCAA[A/G]TGTTTAAATCAAGAC | 84669 |
rs532049715 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60269161 | CTAAATGTTTAAAAT[G/T]TTCAATTACATCATA | 84669 |
rs532074770 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60388181 | TCACTCAGCTACTAA[C/G]AGCAATATAAATGCC | 84669 |
rs532102054 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60336687 | CGCCACTGCACTCCA[C/G]CCTGGGAGACAGAGC | 84669 |
rs532126622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221830 | TCCCACCAAAACATC[C/T]TGTTATATTTTACTT | 84669 |
rs532126670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229542 | GAAGATTTAGATTTA[C/T]TTAGTTTTCAGGTCA | 84669 |
rs532126689 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60381793 | GCTTGACTGAATTTT[C/T]AGGGATGCATCCAAG | 84669 |
rs532145510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60182738 | TGCACCACTGCACTC[C/T]AGCCTGGGTGACAGA | 84669 |
rs532156911 | snp | A/C/G | 3.29516e-05 | 0.00405891 | missense | USP32 | GRCh38.p7 | 17:60183348 | GAGCCGGGTCTCTTG[A/C/G]TACCAAAAAAGCACT | 84669 |
rs532171813 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60201380 | TTGTACATATCTCCT[A/G]GTACACATATCTCTT | 84669 |
rs532177738 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405361 | GCACACACCTCCAAG[A/C]CAACCTAATTTTTTT | 84669 |
rs532192323 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60340716 | ATCCTGTCATTATGA[C/T]GTTAGCTGGTTATTT | 84669 |
rs532209690 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60221791 | TTACAGGTGGAAGAG[C/T]GTTTCTTAATATACC | 84669 |
rs532231968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339733 | CTTTTGCTCTAAAAA[G/T]ATAAAGCTACTGTTT | 84669 |
rs532239127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411104 | GAGGCCGAGGCAGGC[A/G]GATCACCTGAGGTTG | 84669 |
rs532254191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243066 | AGTGCACAAGTCTTG[C/T]ACTTCTTTTGTTGAA | 84669 |
rs532270395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60191350 | GAGGTTGCAGTGAGC[C/T]GAGGTTGCACCACTG | 84669 |
rs532276889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401221 | AGCACTTTGGGGGGC[A/C]AAGGTGGGCGTGGTG | 84669 |
rs532280467 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60324820 | CCAGCCTGACCAACA[C/T]GGAGAAAACCCCCTC | 84669 |
rs532303271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356524 | CCAAGGCTGAACTTA[C/T]AGGTTCAAGGCATTT | 84669 |
rs532306595 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419144 | GGTAGACTGAATAAA[A/G]AAAATGTGGTAATAT | 84669 |
rs532307327 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60347639 | ATTACAGGCGTGAGC[C/T]ACCGCGCCCGGCCTA | 84669 |
rs532313757 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195526 | CATTTTTAGTAGAGA[C/T]GGGGTTTTGCCATGT | 84669 |
rs532314899 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366221 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 84669 |
rs532338860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60364434 | ACCCAGGCTAGAGTG[C/T]GGTGGCGCGATGTCC | 84669 |
rs532344250 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60198795 | AAGGGCTTTTAAACA[A/C]TTAAGGCTCTTTCTT | 84669 |
rs532345550 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60257683 | AAAACAAGGTCTAGT[G/T]ATGTTGCCCAGGCTG | 84669 |
rs532365634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306881 | TACAATTTATATACA[A/T]CAACAGTAAACAATC | 84669 |
rs532373142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381036 | TCATGAGACAAAATT[C/T]ACTCTAGAAAGCACA | 84669 |
rs532375056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60371676 | TTAATCCACATTGAG[A/G]TACTACTTTCCAACA | 84669 |
rs532385568 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60369572 | AAAATGTAAAACTTC[A/C]GAAGTGAAACAGAAA | 84669 |
rs532400089 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419923 | GGAGTGCAGGGGCAT[A/G]GTCTTGGCTCACTGC | 84669 |
rs532426553 | in-del | -/ACAC | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60275508 | GTTTTATACATACAT[-/ACAC]ACACACACATACCCC | 84669 |
rs532437188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412420 | TGGGGGCGGTGGGGC[C/G]GGGGAGCAGGTGGCT | 84669 |
rs532445873 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403738 | TATATATTTGAAGAC[C/T]ATATACATACAGAAA | 84669 |
rs532466582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60220421 | TTACTACGTTCTACT[A/T]GCGTAACCAGTCTGT | 84669 |
rs532486954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265045 | TTCTTCGACTTCATA[G/T]AAATGGAATCATACA | 84669 |
rs532506530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265718 | CAAGTATTTTTATAA[C/T]TACCATAGATTCTCA | 84669 |
rs532508884 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60330037 | TTCTGGGTTGTAACT[A/C]CCTTTCCACTCACTA | 84669 |
rs532541558 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60204973 | TTTTTTTTTTTTTTT[A/G]GAAGAGACGAGGTCT | 84669 |
rs532547441 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60226994 | AGTAAGCTGAGATTG[C/T]GCCACTGTACTCCAG | 84669 |
rs532555078 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60250007 | AAATAAAACTGAAAA[C/T]GAATAAACAAATTTT | 84669 |
rs532568991 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60240294 | TTTCACTGACTGCTA[G/T]AGTTGTTTGTTTAGT | 84669 |
rs532577103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388094 | CTTCAGTAAAAATCT[A/G]CTGAATTAATGAGCA | 84669 |
rs532580503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60322901 | GTCCATTTGATCAAG[A/G]AATTTGAACATCTGG | 84669 |
rs532584214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221131 | AGGTGCAGTGGCTCA[C/T]GCCTGTAATACCAGC | 84669 |
rs532586098 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60341156 | ATGTGTCTTGGGGTT[G/T]CTCTTCTTGAGGAGT | 84669 |
rs532593597 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60256035 | TCAAACAACAGACAT[A/G]TGAGAGATTTAATAG | 84669 |
rs532597749 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409050 | TTGCCAGCTGACTCA[A/C]AGTAAAACTTTTCTC | 84669 |
rs532604505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60331134 | GAAAAGGAAATGATA[G/T]TTCTGTCCAATAGTC | 84669 |
rs532609871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60226369 | AAAAACATTCTAATA[C/G]ATAGCTATATTTTAA | 84669 |
rs532609889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234343 | TGGTCTCGATCTCCC[A/G]ACCTCGTGATCCGCC | 84669 |
rs532615268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60395749 | TTAAAGCACAGGAGA[C/T]TGGCATGTAATTTCT | 84669 |
rs532619376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60180498 | ATGTTCCCCAGTTCT[A/G]TTGATATTCTGTTTC | 84669 |
rs532648386 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378711 | TACGATTCTATTTAC[A/C]TGAAGTATCTAGAAT | 84669 |
rs532663724 | in-del | -/AT | 0.306666 | 0.243493 | intron-variant | USP32 | GRCh38.p7 | 17:60349668 | CATATATATACACAT[-/AT]ATATATATACACACA | 84669 |
rs532689636 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60345667 | AAGAGGTGTCTCATA[A/C]TTTTTTTCAACCTGG | 84669 |
rs532689947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355264 | AGGTCAGAACAGTTA[C/T]TGCCTCTGAGGATGT | 84669 |
rs532696160 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60224062 | GTATCTATGAACTCA[A/G]TGTCCACAAGTTCTT | 84669 |
rs532698719 | snp | C/T | 3.29489e-05 | 0.00405874 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181507 | AGTGACCAACTCTGG[C/T]TGGCTGCCCCCCAGC | 84669 |
rs532713894 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60240272 | TTCCCTCCACCTCAG[C/G]GTTTGCTTTCACTGA | 84669 |
rs532728308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60188947 | CACTGAAAGTGGAAG[C/T]AGGGTGAGATTTAAC | 84669 |
rs532756132 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60204538 | CTGTGGCGCAATCTT[C/T]GCTCACTGCAACCTC | 84669 |
rs532770176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218018 | TTGGGATTACAGGCA[G/T]CAGCCACCATGCCCA | 84669 |
rs532772987 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60280363 | CAGCCTCCCAAAGTG[A/G]TGGGATTACAGGCTC | 84669 |
rs532795330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60394953 | TTCACCATGTTGGCC[A/G]GGCTGGTCTCGAACT | 84669 |
rs532821524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318457 | AGCAGCAGGGAAAAG[C/G]ACTTGTTCACATCTC | 84669 |
rs532832414 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | USP32 | GRCh38.p7 | 17:60217270 | ACTAAAAGTGCAACA[A/C]CACATCTTGCCTCTC | 84669 |
rs532839081 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60273064 | ACCTCTGCCACCCAC[C/G]TGGGTTCAAGAGATT | 84669 |
rs532869680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60269017 | AAAAAGATCATTTTA[A/G]TATTTGACAAAATTA | 84669 |
rs532874385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297487 | AGAGTCTTGCCCTGT[C/T]GCCCAGGTTGGAGTG | 84669 |
rs532905979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60376447 | TATTAATTTTAAACA[C/T]AGTATTAAAGTATTA | 84669 |
rs532938463 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415526 | ATATCTTTGGGGCTA[C/G]ACCTCTTTGATGAGT | 84669 |
rs532941438 | snp | G/T | 3.29755e-05 | 0.00406038 | missense | USP32 | GRCh38.p7 | 17:60223467 | CCCCTGGTTTCTGAG[G/T]GTTAAGGTGCAACAA | 84669 |
rs532945660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60201338 | TTCATTTTGGGGCTA[C/T]TATAGATAATGGTGC | 84669 |
rs532953990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60310597 | CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 84669 |
rs532970943 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177457 | ATAGTTAATTTAATA[A/C]ATTTTCTGCTAGTTC | 84669 |
rs532988327 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60395101 | TAGAAAAGGTACAGT[G/T]TAAAAAGCAGTGTAA | 84669 |
rs532991007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60309980 | ACCTGGGAGGTGGAG[A/G]TTGCAGTGAGCCGAG | 84669 |
rs532992905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423572 | GGGTTCCAGCAATTC[C/T]CCTGCCCCAGCCTCC | 84669 |
rs533005918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185860 | TGAGTCCAGGAGTTC[A/G]AAACCAGCCTGGTCA | 84669 |
rs533006891 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60359075 | CCTCTGCCTATGAGC[G/T]CCAATCATACTCTGA | 84669 |
rs533007448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60334364 | ATAAAATAAACTAGT[A/G]TCTACTTGTATTTTA | 84669 |
rs533010451 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60319803 | AAATAAAAATAATAC[A/G]AAATTTAAAAATACA | 84669 |
rs533016219 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388139 | AATATGAATCCATAA[C/T]ATAACTTTTTGACAC | 84669 |
rs533021803 | snp | C/G | 0.000142184 | 0.00843042 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231545 | GGAAAACAAGGCTGC[C/G]CCACTCGTGGCAGTC | 84669 |
rs533028007 | in-del | -/A | 0.0162398 | 0.0886349 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178077 | ACTACTGTAAAATTT[-/A]AAAAAAAAGACAAAT | 84669 |
rs533032257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237711 | TATGTCTGGCTTCCT[C/T]CATTTAACATGTTTG | 84669 |
rs533032264 | snp | A/G | 1.67033e-05 | 0.00288987 | missense, intron-variant | USP32 | GRCh38.p7 | 17:60391893 | TCACCTCTCCTCAGC[A/G]CCTCCTCGTAGCTGA | 84669 |
rs533053210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326631 | TCTACTGGGACTTAA[C/T]ACTTATAGCAGCAGC | 84669 |
rs533069284 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60239287 | TTGGCTTTGTAAAAT[-/AC]AGTTTCATTATAATG | 84669 |
rs533077577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60341848 | TGCGATGGGTTCGAA[C/T]ATACTCCTTTAGCTC | 84669 |
rs533094585 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | USP32 | GRCh38.p7 | 17:60268407 | GACACTATCTCTATT[A/T]AAAAAAAAAAAAAAA | 84669 |
rs533099203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60351471 | ATGGAGTCTCACTCC[A/G]TCCCCCAGGCTGGAA | 84669 |
rs533104090 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182619 | AATACAAAAATTAGC[C/T]AGGTGCAGTGGTGCA | 84669 |
rs533106937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60293138 | AGATTTTCTCTATTA[C/T]CACCTTCTTCCTTTA | 84669 |
rs533119935 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60256718 | CAATGCCTGCACCAC[A/G]GCAACAGAAGAACTT | 84669 |
rs533123456 | snp | A/T | | | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231432 | ACAGCTTTGGGCAAT[A/T]ATAAAACCTAAGGAC | 84669 |
rs533123603 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60188060 | ATCACAGCTCACTGC[A/G]GCCTTGATCTCTTGG | 84669 |
rs533126866 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60220425 | TACGTTCTACTTGCG[C/T]AACCAGTCTGTTCAC | 84669 |
rs533130098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384654 | AAATTAGTCGGGCAT[A/G]GTGGCACCGTGCCTG | 84669 |
rs533166811 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179029 | ACAGGCTAATGGTGG[C/G]ATCTGCCTGAAAGTT | 84669 |
rs533168132 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392547 | AGCAGCTGACGGTTA[C/G]TGTGGCAGTTGCCGG | 84669 |
rs533169772 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60200368 | GGAGTTCGAGACAGC[C/T]TGACCAACATAGAGA | 84669 |
rs533183393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60276157 | GCCGAGGTAAGAGGA[C/T]TGCTTAAGTCTAGGG | 84669 |
rs533188285 | in-del | -/ATT | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60387717 | TAAGTTGAAAATATC[-/ATT]AAGTCAAAAATGTAT | 84669 |
rs533211379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308877 | GAGGTTGCAGTGAGC[C/T]GAGACTGTGCCACTG | 84669 |
rs533251913 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60249106 | CCTTCTTGGGGTGAG[C/T]CTAACTTACTGGTCA | 84669 |
rs533263613 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60261137 | GGCTATATTTCAAAA[C/T]GCTACTTGTTTATCT | 84669 |
rs533263786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60243838 | TCTGTTGGTGGGTGC[A/G]TATATCATCATTTAT | 84669 |
rs533273284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60237302 | TGTGCTATGCCCAGC[C/T]AATTTTTTTTTTTTT | 84669 |
rs533275471 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60340705 | ATGTGAATTTGATCC[C/T]GTCATTATGATGTTA | 84669 |
rs533278678 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60228507 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTAATT | 84669 |
rs533296349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185294 | TACAAAATATTTGTA[G/T]AAAGATTCATCTCTG | 84669 |
rs533324741 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60292558 | CATTCTGTCACATAG[C/T]CCATAATCAATACGA | 84669 |
rs533345335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308045 | AGGCCCGACTCCAGG[A/G]GAAAACTGCCTTCCC | 84669 |
rs533361706 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412962 | ACGCTCTAAAGTTCC[A/G]AGGTTGCCATTCTGC | 84669 |
rs533368505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301025 | CATGAATCAGTACTT[C/T]ATTCCTTTTTATACC | 84669 |
rs533379963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316149 | CCACTCTGCTATCCA[C/T]GCCAAACATGTAACA | 84669 |
rs533396729 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421378 | CTACCCCTACTTGAA[A/G]CCGCTATGCCCCTCT | 84669 |
rs533426323 | snp | C/T | 0.000381841 | 0.0138121 | synonymous-codon | USP32 | GRCh38.p7 | 17:60214737 | GCCTGTATAGGCTAA[C/T]ACCCGCTTTAAAGGT | 84669 |
rs533439609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60346906 | GCACGGAGTAGCAAA[C/T]GATAAACCTAGAGAG | 84669 |
rs533447727 | in-del | -/CAAAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60213478 | TAAAAACATAATAAT[-/CAAAT]AATAGTTGTTTTGGA | 84669 |
rs533460682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296252 | AAGATATACTGAAGT[C/T]CTAACCTTGAAGTCC | 84669 |
rs533462748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60253620 | AAAATACAAAAATTA[C/G]CTGGGGGTGGTGGCA | 84669 |
rs533463789 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60358967 | TGCAAACCTTAGAAC[C/G]AGAAGGTAGAGACAC | 84669 |
rs533464815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60324339 | AAAACTAACCAGATT[C/T]TAGAAAAAAGTGAAA | 84669 |
rs533476404 | in-del | -/GTTCAAGACCAGCCT | 0.133093 | 0.220981 | intron-variant | USP32 | GRCh38.p7 | 17:60226852 | CACTTGAGGTCAGGA[-/GTTCAAGACCAGCCT]GGCCAAAATGGTGAA | 84669 |
rs533490169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60275167 | TTAATGAATAAATGA[C/G]AAGTATTGGCCGGGC | 84669 |
rs533501015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264594 | AGGCGCAGTGGCTCA[C/T]GCCTATAATCCCAGC | 84669 |
rs533518873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60300857 | TCCATTTCCCTCTCA[C/T]CTGATACCTCCAGCA | 84669 |
rs533518965 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60366754 | AAAAGTTGGTTTTTT[C/T]TTTTTCATGCTGCTT | 84669 |
rs533532305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60365838 | CAGAATAAATCTACC[A/G]AAGAGTTTGGCCTTG | 84669 |
rs533532353 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60375283 | AAAGGTCACACAGAA[C/T]AATCATAATCTTTTC | 84669 |
rs533541012 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60260392 | GCTGGGTGTGGTGGC[A/G]GGTGCCTGTAATCCC | 84669 |
rs533582308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413214 | GTGTTCTGTATCCTG[A/C]CAGTGGGGGAGGGAA | 84669 |
rs533587012 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60251499 | AAGTTTGTATGCACA[A/G]TACTTTCAAGAAAAA | 84669 |
rs533590863 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60422364 | CATCTTGCTCCGTTC[C/T]CTAGTCCAGATCCCA | 84669 |
rs533611021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60215465 | AAATAAAACTCAGTG[A/G]AAAAAAAATTAGGAC | 84669 |
rs533633776 | snp | C/T | 4.94279e-05 | 0.00497107 | missense | USP32 | GRCh38.p7 | 17:60222432 | GTAAGGCCAGGTTTG[C/T]TCCATACCAGTGATA | 84669 |
rs533647673 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60325171 | GTAATCCCAGCATTT[C/T]GGGAGCCTGAGGAGG | 84669 |
rs533652604 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60320729 | ATATAAACCTATTTA[A/G]TAATCAAGGAAGAGT | 84669 |
rs533653976 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60321448 | AGAATCTCATAACAC[A/G]ATATTCCAAATGTCC | 84669 |
rs533660580 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60399360 | TGAAGATTATAATTT[-/A]AAACTAGAATGGGGC | 84669 |
rs533663763 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60267145 | GGGCATGGTGGCTCA[C/T]GCCTGCAATCCCAGT | 84669 |
rs533664060 | in-del | -/GAA | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60361726 | AGCTGTTTAAATAAT[-/GAA]GAAAAATCAATATCC | 84669 |
rs533686132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267348 | GGCGGAGGTTGCAGT[C/G]ATCCAAGATCGTGCC | 84669 |
rs533710632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60275325 | AGTGAGGTGTGGTGG[C/T]GTGTGCCTGTAATCC | 84669 |
rs533726512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373850 | CAGTGTCCAAAAATA[C/T]TTTTTCTTTATATCT | 84669 |
rs533744349 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60358774 | GATATTGAGGATGAC[A/G]GTGCTTCGCAAGGTT | 84669 |
rs533750347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60253095 | TAAGCAAATATAAAG[C/T]ATATGTTTATTCATT | 84669 |
rs533751217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381918 | CCACTATTCTGTCAC[C/T]ATAAATTAGTTTTGC | 84669 |
rs533757740 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60200011 | CCAGCCTGGCCAATA[C/T]GGTGAAACCCTGTCT | 84669 |
rs533764625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60300369 | TAAATCTATATCCCA[C/T]GAAACAGACGGACAC | 84669 |
rs533787430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390320 | AAACACTTCTGAACC[C/T]TGAAGCTGTAAATCA | 84669 |
rs533788989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333196 | AAGCTTTACTAATAG[A/C]CTGACAATCACAAGC | 84669 |
rs533820008 | snp | A/G | 0.000804829 | 0.0200441 | intron-variant | USP32 | GRCh38.p7 | 17:60207918 | GTTGGAAAACTTGGC[A/G]TTTTTTGTTGTTGTT | 84669 |
rs533841512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316271 | AAAAAAAAAATTCTC[C/T]CTTCCCTGTTACTGG | 84669 |
rs533842498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235827 | TAAAATGGGTATAAT[A/G]TTATCTTCCTCACAA | 84669 |
rs533849106 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60359775 | ATGATTGAACCACTA[C/T]ACTCCAGCATTCCAT | 84669 |
rs533859506 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60331908 | CATCTCAAAAAAAAA[A/T]AAAATAAACTTTAAT | 84669 |
rs533877972 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60287467 | ATGAGCCTTGGGGAG[A/G]TTGGGCTTTGAGCAT | 84669 |
rs533886472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348384 | AGAAAGAAAATTGAT[A/G]TGGAATAGTCAGGAG | 84669 |
rs533887751 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60322194 | TTTTTAAGGTTATTT[G/T]AAGATGAGTTCTTGC | 84669 |
rs533910400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243329 | AGTTTTATTTTTCTT[A/T]ACAATCTTGATGCCT | 84669 |
rs533927537 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60374812 | AATAGGAATTTTTCA[C/G]CTCTACTATTATCTT | 84669 |
rs533936988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60191660 | GACTACAGGTGCCCG[C/T]CACCATGCCTGGCTA | 84669 |
rs533964734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60397503 | AGTAGCTGGAACTAC[A/G]GGTGCACACCACCAC | 84669 |
rs533970923 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305684 | AAACACTGAGTTTTT[-/G]GCATCCCTTTCCATT | 84669 |
rs534017726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60274720 | TTTGACAAATGAAGT[A/G]TTTTAGCAGAACCAC | 84669 |
rs534026011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222094 | ATAACCTCTGCATCA[A/C]GCCCTACATTCACTG | 84669 |
rs534049809 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60304812 | TGTTTAAGCCTAACA[C/T]TGACCTCATTAATAA | 84669 |
rs534073082 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60332346 | ACCAAACATTTCTAT[C/T]GCCTCAAAAGTTTAC | 84669 |
rs534102826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249898 | TTAGAGACAAATATT[C/T]GTTTCACCTCATTGC | 84669 |
rs534115961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183614 | ATATGGTTTCATAAA[G/T]GCCTCTACATAGGCC | 84669 |
rs534117636 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60197527 | GAGATTTTTTTGAAC[C/T]CAGGAGGTGGAGGCT | 84669 |
rs534140763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363571 | CCAAGGCTGGAGTAC[A/T]GTAGTGCACTGTAGG | 84669 |
rs534162535 | in-del | -/AACAA | 3.53126e-05 | 0.00420179 | intron-variant | USP32 | GRCh38.p7 | 17:60181276 | ACATGAAGACAAGTG[-/AACAA]AACAAAACACAGACC | 84669 |
rs534174121 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60401287 | AGGCAGGAGAATAGC[A/G]TGAACCAGGGAGGCG | 84669 |
rs534191064 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60323326 | TAAAAAGGAATAAAG[G/T]ACTGATACATGTTTT | 84669 |
rs534195148 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60298923 | AGGCCAGCAGTTAGA[C/G]TCCAGCCTGGGCAAC | 84669 |
rs534228074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405223 | TGTTTTTGTTTTTGA[G/T]ACAGAGTTTCGCTCT | 84669 |
rs534247786 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60225175 | ATAGTGAAAATAGCC[G/T]CATGTGATGGCTCAT | 84669 |
rs534273742 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon | USP32 | GRCh38.p7 | 17:60198274 | CCAATCCTGGGCATG[A/G]TTACTAGCTTCCTGA | 84669 |
rs534275561 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60362283 | AGAAAAATATAGAAT[A/G]AAATCTGTATGTTGT | 84669 |
rs534282091 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60344809 | TGTACATCTGTGTAC[A/C]TAACTACAAAATAGT | 84669 |
rs534297504 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60188976 | ACAGGTCACGTAGGC[C/T]GTTTCCTATAAGCAG | 84669 |
rs534333582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60187150 | AAATTGGCACAGCTC[A/G]AGACATTCAGTTTAG | 84669 |
rs534346313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232354 | ATTTTTATATTTTTA[A/G]TAGAGTCGGGGTTTC | 84669 |
rs534362157 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60258569 | GATGGAGATTAAGAT[A/C/G]CCTTGAATTGTAGGG | 84669 |
rs534378645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60364524 | AGCTCAGATAGGTGC[A/G]CGCCACCATGCCTGG | 84669 |
rs534395025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60195023 | CCCATGTATTCATTA[A/C]CCAACTATAAAAGTC | 84669 |
rs534395907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306502 | AATTAGCTGGGCGTT[A/G]TGGTGGGCGCCTATA | 84669 |
rs534401716 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60206856 | GGGTTCTCTAAATTT[A/T]AGGTTTCTCGTCGAA | 84669 |
rs534404303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60372733 | ATGTGCCTCCAAGCT[A/G]CTGAAGACATTGAGG | 84669 |
rs534409091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353428 | AGTACCAATGGTAAA[G/T]AGACCAACTCCTCCA | 84669 |
rs534412815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60344025 | GGCAACAAGAGCAAA[C/T]CTCTGTCTCAAAGAA | 84669 |
rs534416314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60239360 | AATGAGCTTTTTGAA[C/T]GCGTAGGTTCACGTC | 84669 |
rs534420897 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60386998 | TATACTTTTAAAAGG[C/T]TTAACCGAAACCAAC | 84669 |
rs534424154 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60362853 | AGGAAAAAAAAAAAC[-/A]AAAAACACCTTAGTC | 84669 |
rs534428414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60247262 | TCGGCTCACTGCAAC[C/G]TCCACCTCCCGGTTT | 84669 |
rs534447002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60352581 | GGAAGGCCATTCTAA[G/T]CCATGTTAAAAATCC | 84669 |
rs534473273 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258918 | TCTTTAAAAATACAC[A/G]TGGGAAAAAACCCTA | 84669 |
rs534479839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257807 | TGGTGTTTTTTTTTT[C/T]CTTCAATCTGCTATT | 84669 |
rs534481230 | in-del | -/ATT | | | intron-variant | USP32 | GRCh38.p7 | 17:60241428 | ACAGGCTTTTAAAAA[-/ATT]ATTATTTTTTTTATA | 84669 |
rs534496133 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60202238 | TGTGAACTGGTTTCT[C/G]GGCTCTCTATTCTAT | 84669 |
rs534521102 | snp | A/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60368357 | TCACTATGTAGTAAA[A/T]ATTTTCACTTCATAG | 84669 |
rs534536426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381254 | GACCAGCCTGGGAAA[C/T]AACAGTGAGATTCCC | 84669 |
rs534544247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265336 | AAAGAGATTCAAGCA[C/T]GTATATAAGCGATAC | 84669 |
rs534548617 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60179002 | AGGTGGCTGGTGCCA[A/G]ACCTTTTGTTTACAG | 84669 |
rs534554814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210623 | ACTTCTTTGTATTCT[A/G]CAGATAGAACTATCT | 84669 |
rs534565498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210277 | ATATTAATATAAAAC[G/T]TATATTCATTAGTTT | 84669 |
rs534593514 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417980 | TTTTTTTTTTTGAGA[C/G]GGAGTTTCACTCTTG | 84669 |
rs534595159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60287594 | AGCAGACCCAATTGC[A/G]ATTCTATAACAGGAC | 84669 |
rs534605905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60379900 | TATGCTAAATTTGTG[C/T]TTAAAACAGTCCAAT | 84669 |
rs534608193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60278845 | GATGGCATAGACAGA[C/T]TTAAAATAGTGAAAG | 84669 |
rs534610416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60187828 | GTTTAAATAATCTAT[A/G]AATTACTTATAGGCA | 84669 |
rs534630566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402304 | TGCCCAGGCTGGAGT[A/G]CAGTGGTGCAATCAT | 84669 |
rs534633300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60217435 | GAGTAGCTGGGATTA[C/T]AGACACCTGCCACCA | 84669 |
rs534639232 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60343369 | TCTCAGCACCACATC[G/T]CATTTATTCTAAAAT | 84669 |
rs534643336 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393926 | CAACCTCAGATGATC[C/T]GCCCGCCTCAGCCTC | 84669 |
rs534669514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401591 | GTTAAAAGTAGACCT[C/G]TGGGGGCTGGGTGCA | 84669 |
rs534672305 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409070 | AAACTTTTCTCAGCC[A/G]GGCACAGTGGCTCAT | 84669 |
rs534676622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60294571 | ATAAATATAAAAATG[A/C]CAAGAGTAATCTGCA | 84669 |
rs534691544 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60382626 | ATTATTTAGAACCAA[C/G]AGAGAGCTCTGTGTG | 84669 |
rs534703059 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60387326 | TATCAACTGTTACAT[A/G]CTTAATTATTCCACT | 84669 |
rs534709480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423428 | GAACTCCTGACTTCA[A/G]GTGATCCACCCATCT | 84669 |
rs534728261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60277259 | TCAGGTCTCACCTCA[A/C]CAAAGGCTCCAGCTG | 84669 |
rs534729796 | in-del | -/C | 0.0859336 | 0.188633 | intron-variant | USP32 | GRCh38.p7 | 17:60209724 | TTAATGTCAAATGAC[-/C]CCCCCCCAAAAAAAG | 84669 |
rs534742321 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60396320 | GGGCTCAAGTAATCC[A/C/G]CCTGCCTTAGTCTCC | 84669 |
rs534750422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223864 | GAATTATATGTCCTC[C/T]GACTGGAAGGGAAGA | 84669 |
rs534764621 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392752 | ATGCTCACACCTAGC[A/G]GGAGATCCCTGAGGA | 84669 |
rs534769272 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283718 | CATGGCAGGGAAAGA[G/T]GAATTCACTTTAGAT | 84669 |
rs534778655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326362 | GTCGCCCCGGCTCGA[A/G]TGGAATGGCGCAATC | 84669 |
rs534779721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60255320 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCATACTGT | 84669 |
rs534788440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60246110 | TGTGCTATTAAACAC[C/T]AGAAGTCATTCATTC | 84669 |
rs534793470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60334563 | CGGGCGTGGTTGCAG[A/G]CGCCTGTAGTCCCAG | 84669 |
rs534821285 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60250014 | ACTGAAAATGAATAA[A/G]CAAATTTTAAAAAAA | 84669 |
rs534824024 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60285800 | TATTAGGATTTAACA[C/T]GTAGAAGAAAAAGAG | 84669 |
rs534825847 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410908 | ACATGGTGAAGCCCC[A/G]TTTCTACTAAAAATA | 84669 |
rs534847757 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60197740 | TGATAGGAAAAAGGG[A/G]AAGAAAACAGAAAAT | 84669 |
rs534883901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60284911 | TTTGATGTCTCCTCT[C/T]TGTAATTTTTCTATC | 84669 |
rs534887000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60310263 | TCCAAAAGAAAGGAA[A/G]TCAATGTATCAAAAA | 84669 |
rs534913269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60262802 | CCCCTAGTTGTTACC[C/T]CTTTTAGGAATCACC | 84669 |
rs534927348 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60281978 | GACTTACGGCTGACT[G/T]GTTTTTAATTTGGGG | 84669 |
rs534927486 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60313272 | TAAAATAAAGTAAGA[C/T]TAAAAAAATGCAAGC | 84669 |
rs534930577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423214 | TTTTTTTTTTTGAGA[C/T]AGAGTCTCACTCTGT | 84669 |
rs534949386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406676 | ACGCGCCACCACGCC[C/T]AGCTAATTTTTGTAT | 84669 |
rs534956550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231237 | TACTTTTTATGCCCT[A/G]TACATAGGTATGTTA | 84669 |
rs534958157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60367646 | AACCCCATCTCTACC[A/G]AAAATACAAAAATGA | 84669 |
rs534971397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60399580 | AGATGGGAGGATTGC[C/G]TGAGCCCAGGAAGTG | 84669 |
rs534986297 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60310904 | GCCAAGCACAGAGAG[A/G]CAAATATCACATGTT | 84669 |
rs534986387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406052 | TTCTCAGCTACTTGG[A/G]AGGCTGAGTTGGGAG | 84669 |
rs534993863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60376861 | CTAACACATTGGCAT[A/G]TCAGTTATCAGTTGG | 84669 |
rs535002930 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60244862 | GTATCGAACTCCTGG[A/C]TTCAAGAGATCCGCC | 84669 |
rs535033507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384964 | AAATACAAAAATTAG[C/T]CAGGTGTTGTCAGGC | 84669 |
rs535043063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60359591 | TGAGATGAGAGGATC[A/T]CTTGAGCCCAGGAGT | 84669 |
rs535053425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60238239 | GTGTCTATTTTTAAA[C/T]TGGGTTGTTTGCTTT | 84669 |
rs535058401 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60216648 | TTGTCTGTAGAAAAG[C/G]CTACATTTAAGTAAT | 84669 |
rs535061561 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60352921 | CTAGAAAGAAAAAAA[C/T]GATCTTTGATGATTT | 84669 |
rs535070342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223033 | GACTTTCAAAATAAA[A/C]TATGTAAGAAATGAA | 84669 |
rs535075131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60384387 | TGTAAAATCCCACTT[C/T]AGCATAGTTTTGCTT | 84669 |
rs535075180 | snp | C/T | 3.55044e-05 | 0.00421319 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231575 | CCTGACGACGATCCT[C/T]GAGGGCTGCTCTTGG | 84669 |
rs535098591 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60358314 | GCATGGTACCTCACA[C/T]CTGTAATCCCAGCAC | 84669 |
rs535134146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408056 | TGAGCTGAGATGTCG[C/T]CACTGCACTCCAGCC | 84669 |
rs535140225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60231005 | TTATCCTAGAACCCT[A/G]GTTTTCAGAAGATAG | 84669 |
rs535141271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60334063 | CTTTTACTGTAATAT[A/G]CCATTTACTGGAAAG | 84669 |
rs535145644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60342847 | GGATTCCCGTGGCTA[A/G]GAAAGGGAAATCCCC | 84669 |
rs535157195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60245888 | GCTTTAAAAATATTT[C/G]TATTAAAAAATTATA | 84669 |
rs535173313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201374 | ATATTCTTGTACATA[G/T]CTCCTGGTACACATA | 84669 |
rs535180789 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60342063 | ATCTTTGGTCTTTGA[G/T]GTTGGTGACCCCCAG | 84669 |
rs535214275 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60392103 | CGGCGGCTCCTCCCG[C/G]TCGCCGCCACCGCCT | 84669 |
rs535231097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60184826 | AAAAAAAAAAAAAAA[A/C]AAACATATAAATATC | 84669 |
rs535235800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60359780 | TGAACCACTATACTC[C/T]AGCATTCCATAAAGA | 84669 |
rs535246489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400144 | TAATTTTTGTATTTT[C/T]AGTAGAAACGGGGTT | 84669 |
rs535253977 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60212114 | CTGGAAGGACAGATA[C/G]GAATGTGTTAATTTC | 84669 |
rs535254602 | snp | C/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60210007 | AAAATAATATGTGTA[C/T]ACATTATTTTATATA | 84669 |
rs535267425 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60367459 | GGCTGCAGTGAGTCC[A/G]AATCATGCCACTGCA | 84669 |
rs535279803 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60310121 | GGAGAAAGGGAAACT[C/T]TTGTACACCATTTGC | 84669 |
rs535300088 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60376678 | ACAGGTGCCTGCCAT[A/C]ACGCCCAGCTAATTT | 84669 |
rs535310378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60209193 | TCTATTTTCATTAAA[C/T]GTATTTTTGTTTTGG | 84669 |
rs535311107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200646 | AGAAACAGAATATAG[C/T]GAACACTCAAAAGCC | 84669 |
rs535317967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317979 | GACAGAGCCAGACTC[C/T]GTCTCAAGAAAACAG | 84669 |
rs535327802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236757 | CAATTCCTATTACCA[C/T]CCTCAGCAACAGGAA | 84669 |
rs535377380 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60349446 | TTAGCCAGCCGTGGC[A/G]GTGGGTGCCTGTAAT | 84669 |
rs535408630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222952 | CTCCCAAAGTGCTAG[A/G]ATTACAGGCATGAGC | 84669 |
rs535425974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194884 | CTTGCCTCTTTACCC[A/T]CTGTCCCTGAAAATA | 84669 |
rs535438236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186198 | TGAAAAATTTTTGAA[C/T]GCTTCAAAATGACAA | 84669 |
rs535439001 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60180183 | GGCACGCGCCAACAC[A/G]CCCAACTAATTTTTG | 84669 |
rs535442332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60294432 | TGTTAGTGTGAGTAT[A/G]TAGAATTGTGTTTCA | 84669 |
rs535462160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400955 | TTGAGCCCAGCAGTT[C/T]GAGACCAGCCTGGCC | 84669 |
rs535477188 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60176908 | ACAATAGGGTTCGTT[C/T]TCCTGTGAGAATGGC | 84669 |
rs535483685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60284604 | ATTTTCAAATAAAAC[A/G]GAGCCATTTTTAACA | 84669 |
rs535492373 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388859 | TGTAACTGAAGTCAC[C/T]AGACTGCCCTTCCAC | 84669 |
rs535493455 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60302137 | TTTATTTATTTATTT[A/G]TTTATTTATTTATTT | 84669 |
rs535498524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333898 | GTATCAAACAATTCA[A/G]TTTTTTCCTATAATG | 84669 |
rs535503277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234454 | TTTTTTGGACCGGGC[A/G]TGGTGGTTCACGCCT | 84669 |
rs535504024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60383299 | AAAGGAAAAGAAATT[C/T]TGAGGTGGATACATA | 84669 |
rs535505075 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60193313 | TCCATGACAAGAACA[C/T]CGACACATTGCAGAA | 84669 |
rs535524929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60351896 | GAGTTCCAAAATAGG[C/G]AATAATTAGGAAGTG | 84669 |
rs535535155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333519 | GCAGGAGAGTCACTT[A/G]AACCCGGGAGGTGGA | 84669 |
rs535548315 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60307096 | TAATTAATTTTTTTT[-/C]CTTTCTTTTTTTTTT | 84669 |
rs535553851 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60348318 | ACACACCAAAACTAG[A/C]AGAAGCCAGTGTTTC | 84669 |
rs535554008 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60385047 | AGATGGCCTGAAGCA[A/C]CTGAAGAATCACAAA | 84669 |
rs535558681 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60341960 | GCTGGCGAGGAGCTG[C/T]GATCCTTTGGAGGAG | 84669 |
rs535620350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200840 | ATTTATAAATAGAAT[C/T]ACTTAATTCATTTTT | 84669 |
rs535646426 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60192425 | AAACTTATCTATTGA[A/C]CTCAAAAGGAAGTGA | 84669 |
rs535647435 | in-del | -/ACTT | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403676 | GTCGTGATGTATTGA[-/ACTT]ACTTTTAAATGCTTC | 84669 |
rs535667012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60309492 | TTGTAATCACAGTTA[C/T]TCGGGAGGCTGAGGT | 84669 |
rs535674224 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60266934 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 84669 |
rs535689639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423065 | TTCCTTGTTCTCCCC[A/G]AACACAGACTAGAAT | 84669 |
rs535689764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60300260 | TTATGAATGCTTTTG[A/G]TAAGGCAGATCTGTC | 84669 |
rs535727002 | snp | A/G | 0.000339041 | 0.0130156 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422653 | GAGCAGGTGAAGTGG[A/G]GTGTGAGGGAGGGAG | 84669 |
rs535727134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60241672 | ATGTACTTACATGTA[C/T]GGTTAAGAGTCTATT | 84669 |
rs535730405 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60277845 | AAGACAGAATAGATA[C/T]ATGTTTTCTTCCAAA | 84669 |
rs535751546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60252823 | TGGCAAATAAAAGCA[G/T]AATTCAATATTGTAT | 84669 |
rs535762183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348591 | ACCACCCTAGGCAAC[A/T]TAGTGAGACCCTGTC | 84669 |
rs535762927 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60207352 | TTTTCACAGGAAGAA[C/G]TGTGTTATATACGAC | 84669 |
rs535765427 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60246404 | ATGTGTGTGTGTATA[C/T]ATATATATATTTTTT | 84669 |
rs535777878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267872 | CTGGAGTGCAATGGC[A/G]CAATCTTGGCTCACT | 84669 |
rs535791484 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60375689 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 84669 |
rs535826718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60384281 | ACCAAAAGGCAACCA[C/T]AGCAAATGTTAAAAG | 84669 |
rs535873857 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60392035 | GTGACGGTGACGGTG[C/T]CGGCGTCCCCCGCCC | 84669 |
rs535879920 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60222733 | GTCACCCAGGCTGGA[C/G]TACAGTGGCGCGATC | 84669 |
rs535885155 | in-del | -/A | 0.339429 | 0.233457 | intron-variant | USP32 | GRCh38.p7 | 17:60338325 | GCAAGACTCTATCTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs535887117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330524 | TCTCTCTCTCCCCCC[C/T]TCCCTCCTTTCTCTC | 84669 |
rs535891944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271612 | AAAAATAATCACGAC[C/T]AAAAACAAAACTGAA | 84669 |
rs535900178 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60219984 | TCCGAAACCCATTTC[C/G]TAAGATTATAACTCC | 84669 |
rs535911642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60391337 | ACGGTGAAGGGTGGC[A/G]GAAGCGGATGGCCAC | 84669 |
rs535922235 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60270030 | TAAAGCAAAGGAAGA[C/T]ACACTATGCAACATA | 84669 |
rs535942590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229970 | AGGCACGCACCACTG[C/T]GCCTGGCTAATTTTT | 84669 |
rs535949992 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232366 | TTAGTAGAGTCGGGG[A/T]TTCACCATGTTGGCC | 84669 |
rs535964102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236624 | ACTTACCTATTTTAA[A/G]TGTACAACTCAGTGA | 84669 |
rs535975076 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60180914 | TTGAGACAGGGACTT[G/T]CTCTATCACCCAGGC | 84669 |
rs536000218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280618 | TGTAATTCCTTTTTG[C/T]TTCCTAGATACCTTG | 84669 |
rs536006717 | in-del | -/AT | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60209949 | TAGTATATACATAAC[-/AT]ATGCATAAAATAATG | 84669 |
rs536013282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60345724 | CAGTGGCTCACGCCT[A/G]TAATCCCAGTACTTT | 84669 |
rs536036676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288294 | AAGATAAAAAAATTA[A/G]CCAGGCATGGTGGCG | 84669 |
rs536047607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60395165 | CTTTGACTGAAACAC[A/G]ACTGTAGCTCATGAC | 84669 |
rs536050935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60188049 | GCACTGGCGAGATCA[C/T]AGCTCACTGCAGCCT | 84669 |
rs536052685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297047 | CAGAAAAATCCCAAA[C/T]TGTAAACAAAACCTA | 84669 |
rs536083608 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60302320 | GCCAGGCTAACTTTG[C/T]ATTTTTAGTAGAGAT | 84669 |
rs536083626 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60266403 | ACAATAAATATTACA[A/G]TACCTTACAAGTTTT | 84669 |
rs536088947 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60286746 | TGTCCCTGAGTTGTC[A/T]TTCAGAAGCACAGAC | 84669 |
rs536110065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409952 | AAGGGTTGGACAAGC[G/T]TGGTTTAAAACAAAG | 84669 |
rs536126750 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60196124 | ATACAAAAATTAGCC[A/G]AGTGTGGTGGCATGC | 84669 |
rs536135302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60243414 | ATAAGTGCGGCAAAA[A/G]CAAGTATCCTTTCCT | 84669 |
rs536138398 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60323742 | GCTTTTTATATCTCA[C/T]CTAAAATTTCTGAAA | 84669 |
rs536144414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417584 | TCAGCCTCCTGAGTA[A/G]CTGGGATTACAGGTG | 84669 |
rs536146310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409165 | CCACCCTGAGCAACA[A/T]GGCGAAACCCTGTCT | 84669 |
rs536147617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358417 | CCATCTCTACCAAAA[A/G]TACAAAAATTAGCCA | 84669 |
rs536186340 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60252061 | ATCTTTCTCTGCTTC[G/T]TTTTGTTTAGCTCTA | 84669 |
rs536202689 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60197974 | TACTCTCTACTTTTG[A/C]AACACAGAAGACAGG | 84669 |
rs536206994 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60256515 | TATAATGTTAATGGG[C/G]GAAAAAATGGATTCC | 84669 |
rs536215751 | in-del | -/A | 0.175576 | 0.238665 | intron-variant | USP32 | GRCh38.p7 | 17:60270824 | GCAAAACTCTGCCTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs536230058 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60380631 | CCACTTAATGCTTAT[C/T]GTAGAGAAGTGGTTA | 84669 |
rs536241769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60304338 | TTCAAAAAGAAAAGA[C/T]ATTTTGCTTCCCTTT | 84669 |
rs536263571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369384 | TCACTTGAACCCAGA[A/C]GTTCAAGACACCCTA | 84669 |
rs536267371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281260 | AACACATGCTCTGGC[C/T]GGGTGCAGTGGCTCA | 84669 |
rs536277848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227245 | TCTATTTCTGGCAAG[C/T]GACACTAGTTTTCTT | 84669 |
rs536289166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416910 | ATATATGTATGTATA[C/T]ATCCAATTCCTTTTT | 84669 |
rs536297810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60396052 | TTGTATTTTTATGTA[A/C]ACTAAAGCACTTGAA | 84669 |
rs536348198 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60234437 | CTAATTTAAAAAAAA[A/T]TTTTTTTGGACCGGG | 84669 |
rs536351134 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308493 | CAGACACACAGACCA[A/G]TGGACGACAGAGAAC | 84669 |
rs536375023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60270614 | AGATCACCTGAGATC[A/G]GGGATTCAAGACCAG | 84669 |
rs536395501 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378358 | GGTGGAAATATAAAA[A/C]GGTACAGAAGCTGTG | 84669 |
rs536407459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60269763 | TGGCAGAAAATACAT[C/T]ACAATCCTTTAGTGT | 84669 |
rs536418838 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60240572 | AATGGCGCTGTGCTG[C/G]GGCATTCCTACAATG | 84669 |
rs536438089 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60375448 | CATTGAGTACTTAAA[A/G]GAACGTCTACAATGC | 84669 |
rs536447741 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60370640 | GGCATGGTGGTGCCC[A/C]CCCAACCACTCAGGA | 84669 |
rs536453430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196781 | GTTGAGCCGAGATTG[C/T]ACCACTGCACTCCAG | 84669 |
rs536463013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60385660 | CAGCCTGGCCAACAT[A/G]GTAAAACCCTGTCTC | 84669 |
rs536478940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60224779 | CAGAGTGACACCCTG[A/T]CTCTTTAAGTAAATA | 84669 |
rs536498040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305213 | AGCCTGTATAAGCAT[G/T]GCACCAGCATCTGCT | 84669 |
rs536500482 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393810 | CTGCCTCAGCCTCCC[A/G]AGTAGTTGGGATTAC | 84669 |
rs536502183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373400 | GGTTACACCAAATTT[A/C]CTAATTTTTTCTTCA | 84669 |
rs536511503 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178371 | CAGAAGCTCTTGTTG[C/T]AACAGGTGCATGTGA | 84669 |
rs536519920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60335972 | TCTCATAAAGACTCA[C/T]TTGGATAGGATCCCA | 84669 |
rs536521215 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP32 | GRCh38.p7 | 17:60203997 | CCCTTTCTACTCTAC[C/T]AAGTTGCCACTATAC | 84669 |
rs536528353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60248847 | CTTTGTTTTTTCCTC[A/G]TATATGGGTCACATT | 84669 |
rs536538485 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60344956 | GGGACGCACAGTGGC[G/T]CCGGTTAAACATATT | 84669 |
rs536539154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354438 | AGAGATAAATAAACA[C/T]TGGGAAATATGCCTT | 84669 |
rs536542478 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201229 | TACTCTATATAACTA[A/C/T]AAATCCATTCATTTT | 84669 |
rs536548554 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60245843 | CTTTAGTTCACCTTC[-/T]TTTTTTTTTAATGTG | 84669 |
rs536551875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60238912 | CAGTGAGCTGTGATG[C/G]TGCCACTGCACTCCA | 84669 |
rs536557964 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60343868 | GAAACCTCGTCTCTA[C/G]TAAAAATACCAAAAA | 84669 |
rs536575702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353736 | ACAGAGTGAGACTCT[A/G]TCTAAAAACAAATAA | 84669 |
rs536575746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362740 | ACACAATTTATCATT[C/T]TCCTGGTTCACAAAC | 84669 |
rs536580456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286829 | GGAACTAAAGACTCA[A/G]TGCTCACCATCCTTC | 84669 |
rs536590165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257038 | CGGCAGCTGTGACAT[A/T]ATGGAGTTGATAACG | 84669 |
rs536664262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60180007 | TCTAGAAGATAGGAG[C/T]TTTTGCATTAACTAA | 84669 |
rs536667317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60255552 | ATCCATCCGCCTTGG[A/C]CTCCCAAAGTGCCGG | 84669 |
rs536684081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225950 | AATGTGAAACTCAGT[C/T]TCAAAAAAAAAAAAA | 84669 |
rs536688106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60328770 | GCCATCACACTCCCC[A/G]GGAGCAGCCAGAGAA | 84669 |
rs536688308 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60278096 | ATTTTTTGTAGAGAC[A/G]GGCCTTGCTGTTTCC | 84669 |
rs536706900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210766 | TATAAGATGTTTGAC[A/C]AATTAGTAAAATGAA | 84669 |
rs536715922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60311300 | AAAAACACTCTTAAA[C/T]ATTTTGTAGCCATGA | 84669 |
rs536717900 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306182 | GTGCCACACTCATTA[C/T]TAATTAGCTTTCATT | 84669 |
rs536742380 | in-del | -/TA | | | intron-variant | USP32 | GRCh38.p7 | 17:60238229 | CCATTTTTAGGTGTC[-/TA]TTTTTAAATTGGGTT | 84669 |
rs536749500 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60274414 | CTAAAATTCATGAAA[A/T]CTATATTCCCACAGA | 84669 |
rs536766195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424216 | ACCCTGCCTCCAACA[C/T]TGGGGATCACGTTTC | 84669 |
rs536774829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225691 | AGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 84669 |
rs536780500 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60202080 | TCAAATTTAGCTCTA[C/T]AGAACACCTGGAATT | 84669 |
rs536800596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353566 | GCCAACACGGAGAAA[A/C]ACCATCTCTACTAAA | 84669 |
rs536802534 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60273853 | TAGTCCCAGCTACTC[A/C]GGAGGCTGAGGCAGG | 84669 |
rs536805341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234856 | TCCCGAGATTACAGG[C/T]CCAGCCAGACTTCAT | 84669 |
rs536831018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377974 | AAGACCATGAAAGAC[A/C]ATCCACAGATATTAA | 84669 |
rs536839922 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60196011 | GTGCAGCAGCTCACG[C/T]CTGTAATCCCACCAC | 84669 |
rs536878043 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178965 | TATCTGGACAAGCAC[A/T]ATTGAATTCTTATTT | 84669 |
rs536878520 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60338932 | TTTCTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 84669 |
rs536881496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409119 | TTGGGAGGCCGAGGT[A/G]CACGGATCACCTGAG | 84669 |
rs536890361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327649 | GCTGCCGACATGCTC[C/G]AGGCAGTGAGCGAAA | 84669 |
rs536915540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60202261 | TATTCTATCCCAATG[G/T]TCTACTTGTCTTTTC | 84669 |
rs536958891 | snp | A/G | 0.196771 | 0.244268 | intron-variant | USP32 | GRCh38.p7 | 17:60334671 | CACTCCAGCCTGGGC[A/G]ACAAAGCGAGACTCC | 84669 |
rs536977205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60187084 | GGTGAACTTCCTCCA[C/T]GAATTTCCCTTCCTG | 84669 |
rs536986968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60277571 | AACTAAAATGTGGTA[A/G]GGGACCATAATAATA | 84669 |
rs536998053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60262889 | CAGCAGAAATCTTCT[A/G]GACTTTCAAAGTTCA | 84669 |
rs537004946 | snp | C/T | 0.000296516 | 0.0121725 | missense | USP32 | GRCh38.p7 | 17:60180579 | TAACAGTACCACTTG[C/T]AGTTTGGGTTTTTGG | 84669 |
rs537024399 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60321184 | CCAGCTGTATATGAA[A/T]GGATATAAGCCTAAA | 84669 |
rs537031047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60270968 | AAGAAAAAAAGTAGA[C/G]GCACCCTACTGGAGG | 84669 |
rs537045102 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60279698 | AAAACTTAGCCAGGC[C/G]TGGTGGTGTGCGCCT | 84669 |
rs537055632 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60288148 | AAAAAAAAGTCTTGG[C/G]TGGGCACAGTGACTC | 84669 |
rs537058202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377834 | TGGTTTTCTGCAGCT[A/G]TGGGGTCACTCTATC | 84669 |
rs537062887 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60326525 | GCTGGTCTTGAACTC[C/T]TAACCTTGGGTGATC | 84669 |
rs537074239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387102 | AAGGGAGATAAATAC[A/G]CATCCCAGAAGGTAC | 84669 |
rs537076163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234018 | GTAGTGGTGTGATCA[C/T]GGCTCACTGCAGTCT | 84669 |
rs537093930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424001 | TCAGGAAGCTTACAA[C/G]CATGACAGAAGATGA | 84669 |
rs537099496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60319035 | TACGTAAAGTAATTT[C/G]AATCGGCAAATTCAT | 84669 |
rs537100145 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60270953 | AATCTTCTTATGTAA[A/C]AGAAAAAAAGTAGAG | 84669 |
rs537105710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402834 | GAATCCTCTGAAGGC[C/T]TTCTCACTCATGTCT | 84669 |
rs537144561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60239836 | CCTCCCGGGTTCAAG[A/G]GATTCTCCTGCCTCA | 84669 |
rs537146124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60345702 | TAAGAAAAATTGAGG[C/T]TAGGCACAGTGGCTC | 84669 |
rs537170298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281398 | AAAAAATTAGCCAGG[C/T]GCGGTAGCAGGCGCC | 84669 |
rs537177861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60278567 | GTAATAGGACAGAAA[C/G]ACAAAAAAGCAGTTG | 84669 |
rs537194997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60385509 | AAGATTGCGCCACTA[C/T]ACTCCAACCTGGGTG | 84669 |
rs537207404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60247774 | TTGCAACCTCCACCT[C/T]CCCAGTTCAAGCGAT | 84669 |
rs537236457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402371 | TTCTCCCACCTCAGC[C/T]TCCTGAGTAGCTGGG | 84669 |
rs537257489 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60203357 | AGTGAGTGGAGATCA[C/T]GCCACTGCACTCCAG | 84669 |
rs537267451 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392998 | TGTACCATTTTCACA[A/T]TTTCTAAGTGAGTTC | 84669 |
rs537271662 | snp | C/T | 0.000160992 | 0.0089705 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231647 | CATGGGAGAGAGGCA[C/T]GAAAGGTGATTTAAA | 84669 |
rs537312572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60293396 | CTAGATTATCTTTTT[C/T]TCTTACAAGCAAATT | 84669 |
rs537316312 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60379261 | AAGTAGCACTGGCAT[A/C]AATTGAGGCAAATAG | 84669 |
rs537317501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60247350 | ATACCCAACTAGTTT[C/T]TGTACTTTGAGTAGA | 84669 |
rs537322384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408253 | ATAAGAATGATGAAA[C/T]AGCTATTATAACTAT | 84669 |
rs537333251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60238114 | ATTGAGAAGTAGAAT[C/T]TCATTGTTTTGACTT | 84669 |
rs537360185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60245817 | AATTTTCAGTGTTCA[A/T]ATAGGAATGTCTTTA | 84669 |
rs537360472 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60342229 | TTGCCTGGGTATCAC[C/G]AGTAGAGGCTGCAGA | 84669 |
rs537361338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415961 | TCTCCTGCCTCAGCC[C/T]CCTGAGTAGCTATGA | 84669 |
rs537373131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360914 | CAGGCAGATCGCTTG[A/T]AGTCAGGAGTTCGAG | 84669 |
rs537375104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369273 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 84669 |
rs537436014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60307247 | TGGGATTACAGGCAC[A/G]CACCACAATACCCAG | 84669 |
rs537460695 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60302839 | CAGAAATAAGTATTA[C/T]AGTAATCAGAAATAA | 84669 |
rs537462861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258774 | GGTTTTGATTGAAGA[C/T]AAATTGCCATAATAT | 84669 |
rs537466699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60266704 | TCTGTCGCCCAGGCT[A/G]TGGTGCAGTGGAATG | 84669 |
rs537471539 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60349819 | AGATTGAATAAATTA[C/T]TGTATACATTTAGAA | 84669 |
rs537473589 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230791 | GTGAAATAGCTACCT[A/T]TTCATCCGATTAATC | 84669 |
rs537480575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218178 | TCACGAGGTCAGGAG[A/C]TAGAGACCATCCTGG | 84669 |
rs537489582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60206040 | AAAATTTAAATTAGG[C/T]TGGATGAGGCAGCTC | 84669 |
rs537490845 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420627 | AGCCGAGATCACGCC[A/T]TTGCTCCAGCCTGGG | 84669 |
rs537494458 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60210339 | TTTTTGGAGACAGAG[G/T]CTTACTCTGTTGCCC | 84669 |
rs537495414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60224691 | GGTAGGCTAAGACAG[A/G]AGGATCATTTGAGCC | 84669 |
rs537526269 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60290860 | TTAATCAATCATGAT[C/T]GCTAGCGAAGATGTC | 84669 |
rs537558054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60223906 | TGGCTGGGCTTCTAC[A/G]TAGCATCCTTTAATT | 84669 |
rs537562361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60335608 | CATTCAGAAAAGGGA[A/G]AAGTGGAAAACATAC | 84669 |
rs537564417 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60243289 | GTTTTCTACACATAG[A/G]ATCATGTTATCTGCA | 84669 |
rs537574196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274472 | GAAAACTCAAAACCC[A/T]AACAAGGCAAGTCAT | 84669 |
rs537581697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268769 | TTAAATCAATTGAGC[A/G]CATCATAGTACAACA | 84669 |
rs537588765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60376954 | GAAGAGGTATTAGAT[C/G]AATGGCTGACAACAT | 84669 |
rs537591527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60373192 | AACAAGACCCTGTCT[C/T]GAGACAAAACTAAAA | 84669 |
rs537632459 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412194 | TGATGATAATTGCCT[A/G]GGATATTTATGAAAA | 84669 |
rs537637719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390189 | CTTCATTTGTATTTA[C/T]AAACGTACCATCTTA | 84669 |
rs537639227 | in-del | -/CA | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60373710 | CCCGCCTCGTCCTCC[-/CA]CAGTGTTGGGTTACA | 84669 |
rs537674559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60389557 | CGAGAAAAAAAAAAG[C/T]TTCATAAACTTTTTT | 84669 |
rs537676294 | in-del | -/TTGT | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60365974 | CTCGCTCCCTTTTTC[-/TTGT]TGTTGTTGTTGTTTT | 84669 |
rs537686085 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177146 | GAAAGAAATTATTCA[A/C]GTAGGAGAATTAAAA | 84669 |
rs537698659 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60308954 | CAAGAAACTAGACTC[C/T]TCATCTTTCAGCATA | 84669 |
rs537714659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281466 | TTGCTGGAACTCGGA[A/G]GATGGAGGTTGCAGT | 84669 |
rs537737770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231162 | TGTGAGTTGTATAAA[C/T]AGTTTATGTGTTCTA | 84669 |
rs537737854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60342921 | TCACCTCGCCCTCCG[C/T]GGGCTGCACCCATTG | 84669 |
rs537746820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227796 | ATCACAAACAGTTAT[A/C]AATTTCTTTGTTCCT | 84669 |
rs537757327 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60360227 | CACCTGTAATCCCAG[A/C]ACTTTGGGATGCGAG | 84669 |
rs537768661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194191 | TAGGATTACAGGCAC[A/G]CAACACCATACCTGG | 84669 |
rs537774706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60342208 | GAGGTCCACTCAAGA[C/T]CTTGTTTGCCTGGGT | 84669 |
rs537797456 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60262025 | TAAAAACATATAGAG[C/T]ATTATGCTTAAAATC | 84669 |
rs537803135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259454 | TATACGTGTGAGCGC[A/G]CCCTTCAGTGGGATG | 84669 |
rs537807360 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60365448 | ATCAGGCCACTTGCA[A/G]TCCAGCCTGGGTGAC | 84669 |
rs537831749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60207141 | GAAAGTTCTACAGAA[A/G]CAGAAGCAAGATGAG | 84669 |
rs537848179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60396378 | CACCACGCCTGTCCC[A/G]AAGCTATTTTTGTAC | 84669 |
rs537885771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403540 | GAGGTCTAGGATCTC[A/T]TCATCTAGATCAGGT | 84669 |
rs537898049 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60299338 | TTATTTCTTACAATT[A/C]GGGAGGCTAAGAAGT | 84669 |
rs537900639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221871 | GTAAAAAGTGAGTGT[C/T]CAGAGTACCGAGTGC | 84669 |
rs537900671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60214226 | GGATTACAGGCGTGA[A/G]CCACTGTGCTCGGCC | 84669 |
rs537924513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410634 | GATTGCACCACTGCA[C/T]GCCAGCCTGGGCCAC | 84669 |
rs537926125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249696 | CTCACCAAGGATTAG[C/T]AGTTCTTGAATAAAT | 84669 |
rs537943210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332293 | TCGGTTTTGTCATGC[A/G]TATATACCAATCACT | 84669 |
rs537944944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355745 | GGAGACTAAGGTGGG[A/G]GGATCACTAGCGCCT | 84669 |
rs537945028 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414089 | TGTTATCGGCTGGGC[A/G]TGGTGGCTCACGCCT | 84669 |
rs537959606 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60259381 | AACAATGCTGTGATG[C/T]AAAAAAACAAAAAAA | 84669 |
rs537961725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221451 | CTCATCTATACAAAA[C/T]CTTCCTGGCATAAGG | 84669 |
rs537966241 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60293006 | TTGCTATATTCTCTT[A/G]ATGAAAAGTGGTCCT | 84669 |
rs537977791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60363540 | AAAAAATTTGAGACA[A/G]GGTCTCACTCTGTCG | 84669 |
rs538014621 | in-del | -/T/TT | 0.392556 | 0.237222 | intron-variant | USP32 | GRCh38.p7 | 17:60329278 | CAATGTGTGTGTGTG[-/T/TT]TTTTTTTTTTCATGT | 84669 |
rs538015217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363061 | TTGGGAGACCAAGGA[A/G]GGAAGATCACATGAG | 84669 |
rs538034217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204287 | ACACAAACACACAGG[A/G]AACATAAATTTTGTG | 84669 |
rs538046153 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417074 | AGGTATGCACCACCA[C/T]ACCCAGTTAATTTTT | 84669 |
rs538050019 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60397737 | TTTTCCAATTGTCCT[C/G]CATTTTGGACCCCAG | 84669 |
rs538068563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60264280 | ATCCCAGCACTTTGG[A/G]AGGCTGAGGCAGGAC | 84669 |
rs538075968 | in-del | -/A | 0.289424 | 0.246872 | intron-variant | USP32 | GRCh38.p7 | 17:60317515 | AGTGAGACCCTGTCT[-/A]AAAAAAAAAAAAAAA | 84669 |
rs538077819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60331574 | CCATCTCAAAAAAAA[A/T]TAAAATAAACTTTAA | 84669 |
rs538101455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60219941 | CACATTTAAGTTACA[C/T]GGATCTGATTACTGT | 84669 |
rs538104941 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60313080 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 84669 |
rs538116900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339274 | ATGTCTAATGAGATA[C/T]GCACATAAGTGCTAA | 84669 |
rs538136803 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60183560 | TTGGGAATATATAAC[A/G]GAACATTTACTCTTC | 84669 |
rs538142646 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60234935 | TAATATCAAATGCCA[G/T]AGTGGAGAAGGGAAT | 84669 |
rs538156053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60338630 | AGCTACTTGAGAGGC[C/T]GAGGTGAGAGGATTG | 84669 |
rs538169260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60329390 | TATGCTAGGTATGAG[C/T]CCAGACCATAAAATG | 84669 |
rs538170509 | snp | A/C | 5.00388e-05 | 0.00500169 | intron-variant | USP32 | GRCh38.p7 | 17:60190532 | TTTCTCATATAAAAA[A/C]CACCATTTTATGGTG | 84669 |
rs538172391 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60182262 | CTTTAAAAATTATTG[A/G]GAACCTTTAGAACTT | 84669 |
rs538194590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356664 | ATAGCAGGAACAACA[A/C]CAAATAGCAGTAACA | 84669 |
rs538202917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60379737 | CACATGTTACTTAAC[A/G]TTCAGAAGACGTATA | 84669 |
rs538219765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298269 | CTCTTCAGCATAAAT[C/T]TCTGTTCTATTCTCC | 84669 |
rs538225245 | snp | C/T | | | synonymous-codon | USP32 | GRCh38.p7 | 17:60345586 | GAAAGCATCCTTCAG[C/T]CGTTTTAGCTCTACA | 84669 |
rs538230232 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60235960 | ATGTGGAAGTGTAAT[C/G]ACAAAGCCTAGACCA | 84669 |
rs538233136 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404368 | TTCCAAATAAAAAGT[G/T]TTTTTTTAATGTGAT | 84669 |
rs538236216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190142 | CGGGCTGTTAGAAAG[C/T]GAGGATCTTCCTCCT | 84669 |
rs538241872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197354 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 84669 |
rs538287111 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60334655 | CGAGATCGCGCCACT[A/G]CACTCCAGCCTGGGC | 84669 |
rs538305032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60205089 | TGAGCCACTGCACCC[A/G]GCCAGGAGACACAAA | 84669 |
rs538309590 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60196870 | ACTTATTTAAGTAAA[G/T]ATTTATTTAAATCTT | 84669 |
rs538310207 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60357207 | CTAATCCCAGAACTC[-/T]TGAGTGGTCCAGGTG | 84669 |
rs538341956 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60394839 | GCCTCTGCCTCCCAG[A/G]TTCCAGTGATTCTCC | 84669 |
rs538348271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60313765 | ATTACAAAGCTTTAA[C/G]ACAGGATTAAAGAGG | 84669 |
rs538348758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418562 | AAATAAATTATCAAT[A/G]GAGTAAACAGACAAC | 84669 |
rs538350511 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60330798 | TAAACCCAAATATAA[C/T]TTCATATCATAAGGA | 84669 |
rs538368155 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230015 | GACAGGGTTTCGCCA[C/T]GTTGGCCAGGCTGGT | 84669 |
rs538380031 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60282136 | TTTCAATGACTACCA[C/T]GGAAATCAATGCGCA | 84669 |
rs538388665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60272849 | AGGAAAGAGTTATGC[C/G]AAGAAAGGGCTCCAG | 84669 |
rs538408982 | in-del | -/TTTC | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60239730 | GGTTTCATTTATTTA[-/TTTC]TTTATTTATTAGTTT | 84669 |
rs538410893 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60344033 | GAGCAAACCTCTGTC[C/T]CAAAGAAAAAAAGAA | 84669 |
rs538441808 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60380589 | GAAATCACAGAAATA[C/T]GAAATAAGAAGAGCA | 84669 |
rs538442965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281313 | GGAGGCCGAGGCGGA[C/T]GGATCATGAGGTCAG | 84669 |
rs538468692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60181091 | GCCAGGCTGGTCTCA[A/G]ACTCCTGGGCTCAAG | 84669 |
rs538485284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417946 | AGGCGTCCACCACCA[C/T]GTCCGGCTAATCTTT | 84669 |
rs538493271 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60230915 | CTGGCTGCTTGCGGA[A/C]ATTTTTGTTTTTCTA | 84669 |
rs538495638 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60293562 | AAATGCTGGATAAAA[C/T]GTTAGCACCATAACC | 84669 |
rs538510222 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60323557 | ACAACTCTATGAACA[C/T]AGTAAAAGCCACTGA | 84669 |
rs538544032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60226460 | GTGAAGGATTTTGTG[A/C]CACATAAAGTAATTT | 84669 |
rs538557465 | snp | C/T | 0.000142888 | 0.00845124 | intron-variant | USP32 | GRCh38.p7 | 17:60249670 | TTAAATTACCACACA[C/T]TTCCATTGTTCTCAC | 84669 |
rs538566887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60240690 | TTTTCTGAGTGTGTA[C/T]CTTGTTGTTGGCATG | 84669 |
rs538569515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232053 | CAATTAGTAATATTC[A/G]TAAGTAAATATGTCA | 84669 |
rs538580249 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232196 | TTTTTTTTTTGAGAT[A/G]GAGTCTCACTCTGTC | 84669 |
rs538608838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60214194 | TGCTCCAGCCACCTC[A/G]GCCTCCCAAAGTGAT | 84669 |
rs538618494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60373050 | CATGCACCCATAGTC[A/G]CAGCTACTCTATAGG | 84669 |
rs538621808 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420630 | CGAGATCACGCCATT[G/T]CTCCAGCCTGGGCAA | 84669 |
rs538625836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354632 | AGCTACTGCAGAGCC[A/G]CTTCAGGTAGATGAT | 84669 |
rs538638201 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60297223 | GGCAACATAGCGAGA[A/C]CCCTATCTCTACAAA | 84669 |
rs538664466 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60362858 | AAAAAAAAACAAAAA[A/C]CACCTTAGTCAAAAG | 84669 |
rs538680055 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | USP32 | GRCh38.p7 | 17:60389395 | AAAAATACAAAAAAT[A/T]AGCCAGGAGTGGTGG | 84669 |
rs538682394 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410012 | ATCTCCTTGTTCAGC[A/G]ACTAAAACTGCCTTT | 84669 |
rs538695388 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60271947 | CTCCCAAGTAGCTAG[A/G]ACTACATGTGTACGC | 84669 |
rs538732289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417828 | AGAGTCTTGCTGTGT[C/T]GCCCAGGCTGGAGGG | 84669 |
rs538755442 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60227576 | TGCCCATTCAGTTTT[C/T]CTTTTCTTTTTTTTT | 84669 |
rs538810050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263711 | TTGTTCTCATACACA[C/T]GAAATAGAAGTCGAT | 84669 |
rs538826570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60379459 | TCTACCCTTTCAAAA[A/G]TTTAGCTTATCTCTG | 84669 |
rs538826660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369552 | TTCAGATATATGTAA[A/G]AGTAAAAATGTAAAA | 84669 |
rs538833659 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60253553 | GGCAGATCACTTGAG[G/T]TCAGGAGTTTGAGAC | 84669 |
rs538836743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211735 | CAGAAGCAGCAATTA[C/T]TCTTTTTAATTGCTA | 84669 |
rs538839099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190047 | GGTGTTTGGGTCATA[A/G]GGGTGAAACTCTTGT | 84669 |
rs538854373 | in-del | -/ATT | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419860 | ATTATTATTATTATT[-/ATT]TTATTATTATTATTT | 84669 |
rs538855697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60234493 | AGCACTTCGGGAGGC[C/T]GAGGAGGGCAGATCA | 84669 |
rs538881144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60270780 | GTGAGCCGAGATGGC[A/G]CCACTGCACTCCAGC | 84669 |
rs538894523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297706 | TCAGCCTCCCAAAGT[C/G]CTGGGATTACAGGTG | 84669 |
rs538896715 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60364241 | GCAGAGCCCTCATGA[A/G]GTAATCATTCCTGAA | 84669 |
rs538902581 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60225815 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGTGCCT | 84669 |
rs538909735 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60262644 | TTTGTACCCAAGGCC[C/T]TTCAAGATACGTCTC | 84669 |
rs538918543 | snp | C/T | | | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402667 | ATTCTGGGTTGTCAT[C/T]GCTTCATAAGAAATT | 84669 |
rs538925609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234099 | GGACTACAGGCGCAC[A/G]CTACCAAGCATGACT | 84669 |
rs538945511 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60196553 | ATTTTGGCCGGGCAC[A/G]ATGGCTCATGCCTGT | 84669 |
rs538953185 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60234314 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 84669 |
rs538958937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355647 | AGCCTAAGAGTTTAA[C/G]ACCAGCCTGGGCAAC | 84669 |
rs538961788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197344 | GTGTGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 84669 |
rs538967767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60345938 | ACTGAGCCAAGACCA[C/T]GCCGCCGCACTCCAG | 84669 |
rs538973650 | in-del | -/C | 0.00292275 | 0.038116 | intron-variant | USP32 | GRCh38.p7 | 17:60209724 | CTTAATGTCAAATGA[-/C]CCCCCCCAAAAAAAG | 84669 |
rs538986067 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60336879 | AAACCAGTATCCTGC[G/T]GGTTGTTCTGTCAGC | 84669 |
rs538986158 | in-del | -/GAT | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60401829 | TTGTGCACATTTGTA[-/GAT]AATATTAACAAACAA | 84669 |
rs538995536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363484 | AAAAGCGCCACTGCA[A/C]TCCAGCCTGGGTGAC | 84669 |
rs539021597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244892 | CTGCCTTGGCCTCCC[A/G]AAGAGCTGGGATTAC | 84669 |
rs539033097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360212 | AGGCACAGTGGCTCA[C/T]ACCTGTAATCCCAGC | 84669 |
rs539037646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204159 | GATTTTCCTCAAGAA[C/T]ATTCTTGTATCCTCT | 84669 |
rs539058839 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60245893 | AAAAATATTTCTATT[-/A]AAAAATTATATATAA | 84669 |
rs539061730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407632 | CAATGTGACATCCAC[A/G]TTAGCCAGGTGTGGT | 84669 |
rs539082174 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60344690 | GAACTCCTGAGCTCA[A/G]GTGATCCTCCTGCCT | 84669 |
rs539082584 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406945 | GATGGAGTTAAAAGG[G/T]ACCAGATTAACCCTT | 84669 |
rs539096385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414911 | GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTAGC | 84669 |
rs539099479 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60203622 | GCTCTTGTCGCCCAG[C/G]CTGGAGTGCAATGGC | 84669 |
rs539101195 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60335085 | GCCTCAAGTGATCCT[C/T]CCATCTTAGCTTCCC | 84669 |
rs539105441 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60312971 | CTCTGTGGCTGGGCA[C/G/T]GGTGGCTCATGCCTG | 84669 |
rs539124773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60208995 | AAAATCCTATTTTTC[A/G]TTTGTTCTTATCAAG | 84669 |
rs539133857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60253854 | TATAGTGGTGATCTA[C/T]ATTATTTTCATATAT | 84669 |
rs539137802 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60338682 | ATGCAGTGAGCCGAA[A/G]TTGCACCACTGCACT | 84669 |
rs539141922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312181 | GAAAGCAGCCCCTGG[G/T]TGGGAAATACTATCT | 84669 |
rs539143766 | snp | A/C | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60320960 | CTCATTGCTTTTTTT[A/C]CCCCATCTCTGTCCT | 84669 |
rs539167181 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60269321 | AAAACCCTAACATGA[A/G]ATTAATATTTGTTAA | 84669 |
rs539173693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60264231 | CAACCATTTAAAAAA[A/T]TTTTTTAGGCCAGCA | 84669 |
rs539180178 | snp | A/G | 0.000133003 | 0.00815376 | intron-variant | USP32 | GRCh38.p7 | 17:60271299 | ACAAATATGAGATGG[A/G]CTCAGGTATGTTTAC | 84669 |
rs539185855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60253186 | CCAAAAGTCAAAATG[C/T]TATACTCTGTGAGAG | 84669 |
rs539191587 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60366901 | GATCTCGGCTCACTG[A/C]AAGCTCCGCCTCCCA | 84669 |
rs539200731 | snp | C/T | 0.00096249 | 0.0219162 | intron-variant | USP32 | GRCh38.p7 | 17:60219614 | ATGGTATTCTTGCTG[C/T]ATTCTTAAGTTACCT | 84669 |
rs539218377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267808 | ACAGGTGTGAGCCAC[C/T]GTGCCAGGCCTTTTT | 84669 |
rs539230435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375661 | CAGGCTGGAGTGCAG[G/T]GGCACGATCTTGGCT | 84669 |
rs539237322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216405 | TTTATTGAGCAACCC[A/C]ACTTAAAAATATAAA | 84669 |
rs539240304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387666 | TACATTCTTTGATAC[A/G]ACTTACAATGAGATT | 84669 |
rs539248445 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60372936 | AGCTCTGGGAGGCCA[A/G]GGCAGGAGACTTGAG | 84669 |
rs539253619 | snp | C/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423043 | TCAGAGTGGTCTGGA[C/T]GGGATCTTCCTTGTT | 84669 |
rs539299145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60222705 | TTTTTTTTTTGAGAC[A/G]GGGTCTTGTTCCGTC | 84669 |
rs539301600 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60421732 | CCAACTCAGACTACA[C/T]CCGGACTCTGCCCAC | 84669 |
rs539327351 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60194068 | TTTTTTTTGAGACAG[C/G]GTATCACTCTGTTGC | 84669 |
rs539354821 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60179815 | AGCTGGGACTACAGG[G/T]GCGTGCCACCACGCC | 84669 |
rs539354888 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408177 | TTATACCAAGAAGCA[-/G]GGGGGAAAAATCAGG | 84669 |
rs539362576 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60229896 | TTGGGTCACTGCAAC[C/G]TCTGCCTCCTGGGTT | 84669 |
rs539368992 | in-del | -/TCTG | | | intron-variant | USP32 | GRCh38.p7 | 17:60197172 | GTGACAAATTAAGAA[-/TCTG]TCTCAAAAAAAAAAA | 84669 |
rs539373114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60279611 | GGAGGCTGAGGCAGG[A/T]AGATCACTAGAGCCC | 84669 |
rs539389917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60350963 | CTAAGAGACAGTCAA[A/G]TTTTTCTGGTGCACA | 84669 |
rs539398214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60292643 | CTCACTACCTCACTG[C/T]TACACCATGTTCTAA | 84669 |
rs539406025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60341075 | CCTTTGTGGGTAACT[A/C]GACCTTTCTCTCTGG | 84669 |
rs539426196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60359605 | CACTTGAGCCCAGGA[A/G]TTTGAGACCAGCTTG | 84669 |
rs539441279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200699 | ACAAATTCTCCCTTC[C/T]TCACAAAGGTAACTA | 84669 |
rs539441665 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393854 | CATGCCTGGCTAATT[C/T]TGTATTTTCAGTAGA | 84669 |
rs539454192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60291660 | TAGCAATGTTCTACA[C/T]GCAATCATCGACACA | 84669 |
rs539470295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390384 | CCATTGCCTAATTGA[A/G]GCCAGACCTGTCAGG | 84669 |
rs539476569 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236503 | AATTAGAAAAACAAC[A/T]GGTGTTTCCAATTAA | 84669 |
rs539476691 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60360465 | GGAGTTCGAGACCAG[C/G]CTGGCAAACATGGAG | 84669 |
rs539478203 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60352353 | TATTTTTGAGTGAAC[A/G]TCAAAGTTATAAGCC | 84669 |
rs539489743 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60316471 | CAAAGTGCTTCAGTG[A/C]GCACGTTTCCGCAGT | 84669 |
rs539494113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414116 | GCCTATAATCCCAGC[A/G]CTTTGGGAGGCCATG | 84669 |
rs539514233 | snp | C/T | 0.00104167 | 0.0227981 | synonymous-codon, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60294752 | CATTCTTTCCATTTC[C/T]TCCCGTATAACATAG | 84669 |
rs539522021 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60223212 | GAATAACAATAATGC[C/T]AAGGGTTACTAAACT | 84669 |
rs539541319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60340123 | TAGGATTTTGAAAAA[G/T]AACTCACAAGGGTCA | 84669 |
rs539546521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317019 | AAAGTAGACTGGAGG[A/T]TATCAGGGGCTGGGG | 84669 |
rs539572401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60260709 | ATGCTAGATAGAAAA[C/T]TATATACAGATTTAG | 84669 |
rs539573320 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60184039 | CGCCTATAAACCCCG[C/T]GCTTTGGGAGGCCAA | 84669 |
rs539576944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348494 | CAAGATAAAGACTAG[C/G]CCAGGTGCAGTGGCT | 84669 |
rs539588768 | in-del | -/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423196 | TTTTTTTCTTTGTTC[-/T]TTTTTTTTTTTTTGA | 84669 |
rs539597305 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60221483 | AGTTTTAGCTTGGAC[A/G]TTATAAAAGGAAGAG | 84669 |
rs539600595 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60207976 | TCTCTTGGTCACATA[A/G]CCTAACAATTGATCA | 84669 |
rs539603117 | in-del | -/CAAGATCCTGTCTCCAAAAAAACAAACAGA | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264501 | GCCTAGGCAACAGAG[lengthTooLong]CAAAAAAAAAAACAA | 84669 |
rs539619855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60242686 | TGCTGGGATTACAGG[C/G]ATGAGCCACCACGCC | 84669 |
rs539635578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60199058 | CAAGTTGAGGGTACA[C/G]TGAGCTGTGATCGTG | 84669 |
rs539635619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190855 | ATACTTATTAATAAT[C/T]AGTACAGTTTCAGGG | 84669 |
rs539650959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60357106 | AAAACAAAACAATTG[A/C]AAAATTTGAAGACAG | 84669 |
rs539656502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60215580 | GTCCACTTTCCTAAA[C/T]TTTCTTTGAATCACT | 84669 |
rs539693020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316348 | CCTAAGTAAATGACT[A/G]CAAGTGGGAAAATGG | 84669 |
rs539699881 | snp | C/G | 0.000860158 | 0.0207205 | intron-variant | USP32 | GRCh38.p7 | 17:60190714 | AGATCCACAGAGGAA[C/G]AAATAATTATGAAGG | 84669 |
rs539714305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306629 | GGCAACAGAGCAAGA[C/T]TCCGTCTCGAAAGAA | 84669 |
rs539729524 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60287101 | GTTGCAGTGAGCCGA[G/T]ATCGCGCCACTGCAC | 84669 |
rs539772408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60275371 | CTGAGGCAGAAGAAT[C/T]GCTTGAACCTGGGAG | 84669 |
rs539774113 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60217515 | GACCAGGTTGGTCTC[A/G]AACTCCTGACCTCTG | 84669 |
rs539790061 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60364644 | GCCTCCCAAAGTGCC[A/G]GGATTATGGGCGAGA | 84669 |
rs539810924 | in-del | -/TAGCTACT | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60367692 | ACATGCCTATACTTA[-/TAGCTACT]TGGGAGGTTGGGGCA | 84669 |
rs539823044 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60333648 | AAAGAAGGAAGAAAG[-/A]AAGGGAGGGAGAGAA | 84669 |
rs539823579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60291126 | CTACTGTTATACAGT[A/G]GAAGAAAGAGGACTG | 84669 |
rs539829517 | snp | C/G/T | 4.94241e-05 | 0.00497092 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183337 | ATGCTGGCAGAGAGC[C/G/T]GGGTCTCTTGGTACC | 84669 |
rs539830165 | in-del | -/AAGT | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60320360 | AAAATTAATAAAAAC[-/AAGT]AAGATAAATTACTAT | 84669 |
rs539830270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60282702 | TATGAAGTTGTTAAA[A/C]CTTATTTAAACATGA | 84669 |
rs539834169 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60191908 | TAACAGCAATGACCA[A/G]TCAATCTCCGTAACT | 84669 |
rs539834650 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60274931 | AGACCATCCAAACCA[C/T]ACCACCTTCAAAGAT | 84669 |
rs539855444 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60396778 | ACCTTGGAGGTTCTC[-/T]TTTTGTTTTACTACA | 84669 |
rs539864684 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60399331 | GCAGAGGAAGGAGGC[A/C]AGAAGTGCTGAGATG | 84669 |
rs539886874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60290161 | AGCTGCTGAGATGAC[C/T]TGCTGCAACTAATTT | 84669 |
rs539893084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60299268 | CTCTTTGTCCATTTT[A/G]TGCTGCTATAATAAA | 84669 |
rs539895098 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60219291 | CAGTCAATGACTGGT[A/G]TACTACTACTTAGTC | 84669 |
rs539912179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235890 | ATGTGACATATGCAG[C/G]TACCCCCGTACCCAA | 84669 |
rs539915982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60307517 | AGAGAATCCTAAAAC[A/G]TACATGGAACCTCAA | 84669 |
rs539916800 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412412 | GTGGGGAATGGGGGC[A/G]GTGGGGCGGGGGAGC | 84669 |
rs539917155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404665 | TGTAGAAGAGTGCAC[C/T]TCAGCCTCCTTGGAA | 84669 |
rs539955843 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60251898 | AAGTATTATTTTATA[A/T]GATCTAGAGTGAAAA | 84669 |
rs539986195 | snp | G/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420485 | CCAGCGTGACCAACA[G/T]GGAGAAACCCCGTCT | 84669 |
rs539995037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60357718 | AATCTCTGGAAAGGA[C/T]TGGATGACTCAGCAG | 84669 |
rs539996517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258914 | CCATTCTTTAAAAAT[A/G]CACATGGGAAAAAAC | 84669 |
rs540003297 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60299142 | CTCTCTCCTCTGTCC[C/T]CTATCCCCTCCAAAA | 84669 |
rs540004976 | in-del | -/A | 0.0713306 | 0.174864 | intron-variant | USP32 | GRCh38.p7 | 17:60192948 | GAAACAGAAGAGAAC[-/A]AAAAGAGTGTAAGAA | 84669 |
rs540011768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60251922 | GTGAAAATAGGAGCA[A/G]GGAATAAAGTAGGTA | 84669 |
rs540015310 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60389105 | CACACTGGACTAATG[A/T]GTGTTTGTCAAATCC | 84669 |
rs540089108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381486 | CCTTGGACTATTTGC[C/T]TCCTACTCCTCCAAT | 84669 |
rs540098057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306417 | CCGAGGGGGGTGGAT[C/T]ATTTGAGGTCAGGAG | 84669 |
rs540100752 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420375 | TAGATTTTTAAAAAA[G/T]ACTCTTTCCTGGCCG | 84669 |
rs540123933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60250985 | TCTCACATTGTCACC[C/G]AGGCTGGAATGCAAT | 84669 |
rs540123979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259443 | GTGAGTGTGGATATA[C/T]GTGTGAGCGCGCCCT | 84669 |
rs540127444 | in-del | -/GA/GAGA | 0.0876332 | 0.193734 | intron-variant | USP32 | GRCh38.p7 | 17:60240495 | AAGAGAAAAAAGGGA[-/GA/GAGA]GAGAGAGAGAGAGAG | 84669 |
rs540132044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60385086 | AAATGGCAGGTTCCT[A/G]CCTTAACCGATGACA | 84669 |
rs540143183 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419092 | CAGCACTATTCACAA[C/T]AGCAAAGACATGGAA | 84669 |
rs540146194 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353198 | AAGAGACACCAAAGG[G/T]CTCAAGCGCAACATA | 84669 |
rs540151641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221503 | AAAAGGAAGAGTGTT[C/T]CTTTCTTTTTTTTTT | 84669 |
rs540176733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373613 | CACCACCACAACCGG[C/G]TAATTTTTGTATATT | 84669 |
rs540200764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235507 | ATAATAAGCAGTGAC[A/G]GAGGAAATACAGGCA | 84669 |
rs540205596 | in-del | -/AAAT | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60385547 | AAGACTCTGTCTCAA[-/AAAT]AAATAAATAGGCCAG | 84669 |
rs540225014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381021 | ATATTTGCATAAATG[C/T]CATGAGACAAAATTT | 84669 |
rs540244207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348078 | AGTGAGCCAAGATAG[C/T]GCCACTGCACTCCAG | 84669 |
rs540260553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388703 | ATTCAAGCCAAAAAA[A/T]AAAAGCTACCAGTAA | 84669 |
rs540273646 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60347579 | AGGATGGTCTCGATC[C/T]CCTAACCTCGTGATC | 84669 |
rs540278576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60199381 | AATTTGCTTTGAGTA[C/T]GTTAAAGAGATATTT | 84669 |
rs540297317 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60284514 | CATGAGCCACCACGC[C/T]CAGCCTAATTCAAGA | 84669 |
rs540323041 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60319301 | AGTAAAATACAGGGA[C/T]TCAGATTAAGAATAT | 84669 |
rs540334898 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60234303 | TATTTTCAGTAGAGA[C/T]GGGGTTTCACCGTGT | 84669 |
rs540341630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190243 | AGCCTTTGCCAGAAG[C/G]CAGGACCATGTCCTT | 84669 |
rs540351487 | snp | A/C | 0.029116 | 0.117091 | intron-variant | USP32 | GRCh38.p7 | 17:60206199 | GTACACGTTTGTAGT[A/C]CCAGCTACTTGGGAA | 84669 |
rs540364501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60226829 | TTTGGGAGACCGAGG[C/T]AGATGGATCACTTGA | 84669 |
rs540369076 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60251294 | AAAAAATAATAATAA[A/T]AAATAACCGTTTTTA | 84669 |
rs540376656 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60395718 | ATGCCTGCAAAAGGG[A/T]TATCCATATAAAGAT | 84669 |
rs540403635 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60292201 | TCTTGCAGGCTATTT[C/T]TTAGTGGTCTGTTTT | 84669 |
rs540422270 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60312064 | TAATATACCAACTAT[A/G]TGGTCTTAAGCAAAT | 84669 |
rs540423360 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245228 | TATTGGTGCTCTTTA[-/T]TTTTTTTTTTTGGCA | 84669 |
rs540438024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373344 | GCCCTAGGACATTAC[C/G]ATGGAGTACTGCAGT | 84669 |
rs540462080 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283227 | AGCTATAATATAAAA[G/T]TTCATGGTGTGGTCA | 84669 |
rs540462417 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60315022 | TGACTTAAATAAAAA[C/G]ATGCAATGTCTTTAG | 84669 |
rs540472522 | snp | C/G/T | 0.000148251 | 0.00860842 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205606 | TGGTCGGGGTAGGTC[C/G/T]CCATTGGTAGTTAGG | 84669 |
rs540476258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315162 | TAGCACTTTGGGAGG[C/T]CGAGGTGGGCGGAAT | 84669 |
rs540487115 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204421 | TTATAGCTTCAAAAT[A/C]CTGTCCTAAAGGGAT | 84669 |
rs540508712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403158 | CTGGGTCTACAGGCG[C/T]GCGCCACCACGCCCA | 84669 |
rs540520691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60188853 | AACCCTACATGTAGG[A/G]GAGCCCAGATTAGTC | 84669 |
rs540544565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60212454 | GAACATAGAAAAGGC[A/G]CAACTAAAAATACAG | 84669 |
rs540548371 | snp | A/T | | | missense | USP32 | GRCh38.p7 | 17:60181692 | GGCTGCTATTAGGGC[A/T]GCTGTTTTTGCTGGA | 84669 |
rs540552813 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353197 | AAGAGACACCAAAGG[-/T]GCTCAAGCGCAACAT | 84669 |
rs540554181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60322678 | AGTTACATTTATAGA[A/C]CCACCATATAAAATA | 84669 |
rs540596677 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306822 | GTTAGAACTGATAAA[C/T]TGAGGAAAGATTGCA | 84669 |
rs540615497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60272963 | TACAAATGCCGGGAA[A/T]TTTGTTTTGTTTTGT | 84669 |
rs540615987 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60304759 | TCTCATCTTTAAACT[G/T]CCAGTCACCAGGAAA | 84669 |
rs540616129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377245 | CAGGAGGATCTCTTG[A/G]GGCCAAGAGTTTGAG | 84669 |
rs540616474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60248487 | AGACTTTCATTATGC[A/G]TATTTTGGTAGACTT | 84669 |
rs540651808 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306499 | AAAAATTAGCTGGGC[A/G/T]TTGTGGTGGGCGCCT | 84669 |
rs540652389 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227876 | TTAAGTAAAAATGGC[A/T]TAATTATTTATGTAA | 84669 |
rs540653972 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60385223 | GCCCCTGCCTGCAAG[A/T]GAAAAACCCCCTTTG | 84669 |
rs540658727 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60339890 | TATATGTTATTACTT[C/T]TACTATTAAAACAAA | 84669 |
rs540661276 | in-del | -/ATAG | 0.0693013 | 0.172766 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232820 | CAAAGTGCTGGGATA[-/ATAG]ATAGGCGTGAGCCAC | 84669 |
rs540666933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268980 | TGCTTACAAATTATG[C/T]TACAACATTTTAGTT | 84669 |
rs540676792 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360856 | AAAGTAGGCCGGGCG[C/T]GGTGGCTCACACCTA | 84669 |
rs540684272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384647 | AAATACAAAATTAGT[C/T]GGGCATGGTGGCACC | 84669 |
rs540690968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60396569 | CAGTAGCTCACACCC[A/G]AACTGTAATTCCAGT | 84669 |
rs540702198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289029 | GTTTGTTTGTTTGAG[A/G]CGGAGTCTCACTTTG | 84669 |
rs540704308 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | USP32 | GRCh38.p7 | 17:60181440 | AGCCATTGCCACATG[C/T]TTCATGCTCATAAAG | 84669 |
rs540719206 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377253 | TCTCTTGAGGCCAAG[A/G]GTTTGAGACCAGCCT | 84669 |
rs540719684 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231848 | CATAGAAGAATAAAG[C/T]TTGACACATTAAAGC | 84669 |
rs540720848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403592 | AGGTGTGGTTCCTCA[A/G]ATACAATGCCTTTTG | 84669 |
rs540726370 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60329980 | TATGCCCTTGCAATT[A/G]GCTTCACACTGGTTT | 84669 |
rs540732337 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60337058 | TAGCCCTTAATGCTG[C/G]TAAGTCCAACATAAA | 84669 |
rs540773571 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60354140 | ATTACATGGTATAAA[A/T]TATTTCACAATAAAC | 84669 |
rs540797465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60342412 | GGAGACAGTCTGTCC[A/G]TTCTCAGAGCTCAAA | 84669 |
rs540814226 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60288454 | CCTTTATAAGCATAT[G/T]CTCATATTACCAGCC | 84669 |
rs540870331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60193522 | CCTTGCCCTAACAAG[C/G]AGCAATGCAACAATT | 84669 |
rs540875453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297452 | TTTTCCTTTTCTTTT[C/T]TTTTTTTTCTTTTTG | 84669 |
rs540885867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296461 | AAGGAACCCCAAGGA[A/T]TGTCAGTCATCCTAG | 84669 |
rs540888262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305621 | ATTTTGGTGAAATCT[C/G]CTGAAGATTAAACAA | 84669 |
rs540902849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60249049 | GCTGCTCAGTTTCTT[C/T]GTGTTTTCTTTTTTA | 84669 |
rs540913891 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195589 | GTGATTCTCCCACCT[G/T]GGCCTCCCGAAGTGC | 84669 |
rs540925083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60313156 | CTCGGGAGGCTGAGT[A/G]AGGAGAATCGCTTGA | 84669 |
rs540943074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418021 | TGGAGTGCAATGGCA[C/T]GATCTCGGCTCACCA | 84669 |
rs540943152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409454 | AAAATGAAAAATTCA[A/G]CATGGCAGCTGGCTT | 84669 |
rs540954283 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60235462 | TGATGAGATAGATAA[G/T]GTAAAAAGTATGTAA | 84669 |
rs540974816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60309515 | GCTGAGGTGGGAGAA[A/T]CACCTGAGTCCAGGA | 84669 |
rs540986147 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60384648 | AATACAAAATTAGTC[A/G]GGCATGGTGGCACCG | 84669 |
rs541003582 | snp | A/C | | | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419287 | CAAATACCGCATGTT[A/C]TCACTTATAAGTAGG | 84669 |
rs541005659 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60209285 | GATCTCAGAATAGTT[G/T]AGTTTGCATTTAAGT | 84669 |
rs541005770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200325 | CCAGCACTTTGGGAG[A/G]CCAAGGTGGGTGGAT | 84669 |
rs541013011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60385901 | TATGTTAATGAATAC[C/T]AAGTCCCTAATAAAG | 84669 |
rs541013600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60359993 | CTGCCTCAGCCCCCC[G/T]AGTAGCTGGGACTAC | 84669 |
rs541067033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60208476 | TTTGAAACCAAAAAA[A/C]CATGCCCCAGTCTAC | 84669 |
rs541073191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317415 | CAGCGACTCGGGAGG[C/G]TGAGCTGGGAGGATT | 84669 |
rs541076350 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60336916 | GTCAAGATCAAGATA[C/T]ACCGTAACAAAAATG | 84669 |
rs541080943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60383650 | CCATCAGATATGAGA[A/G]TGAGCCAGACATGTA | 84669 |
rs541088438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60276609 | GTATTGAGAATATAA[C/T]AGGTGTTCAATAAGT | 84669 |
rs541094955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186280 | ACATGTGAGCTGGCC[C/G]TCAAGCCAGGGGTGC | 84669 |
rs541108192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316594 | GCCTGTAATCTCAAC[A/C]CTTTGGGAGGCTGAG | 84669 |
rs541115966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422747 | GAAGAACAATGATAG[G/T]GTACCTGAGATAGCA | 84669 |
rs541148784 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60325703 | AAGTTGAGGCTGGCA[A/G]ATCGCTTGAGCCCAG | 84669 |
rs541167466 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416535 | GACTTTGTTGAATGA[C/T]TTGATTTGCCCTATA | 84669 |
rs541203900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267510 | CAATCTTTTTTTGGC[A/T]AAAACAATTTTAACT | 84669 |
rs541204497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407758 | CTGTGCTCCAGCCTG[A/G]GCGACAGAGCAAGCC | 84669 |
rs541208876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60293803 | GAACAATGGAGGACT[A/G]TCATACTGGTGAAAT | 84669 |
rs541231947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60284244 | TTTGAGACCAAGTCT[C/T]GCCCTGTCGCCCAGG | 84669 |
rs541246098 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60367794 | GCCTGGGTGACAGAG[A/T]GAGACCCTGTCTAAA | 84669 |
rs541267847 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407714 | TTGAACCCAGGAGGC[A/G]GAGGTTACAGTGAGC | 84669 |
rs541283289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192582 | TGGGATTACAGGCAC[A/G]CATCACCACGCCCCG | 84669 |
rs541291512 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60275872 | ACCTGCCACCATGCC[C/T]GGCTAATTTTTTGTA | 84669 |
rs541293624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60391487 | CTGTTAGGAACGAGG[G/T]TAGGATGTTATTTGA | 84669 |
rs541296835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60283620 | AGTTAGACACTGGAA[C/T]TAAAAATACTATCAA | 84669 |
rs541305793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407181 | GTTCATGGAACCTGA[A/G]GCAGCTGTGGAAGTT | 84669 |
rs541313073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60276404 | AGATTCCTAAATAAG[A/G]TGTCTGTCTATTCCA | 84669 |
rs541327071 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60247109 | GTCATACCACTCAGA[A/C]AAATGTCCTACAGCA | 84669 |
rs541344715 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414391 | ATAGGGAATAAAATA[A/T]CTCCTGACTCTAACT | 84669 |
rs541397951 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | USP32 | GRCh38.p7 | 17:60261657 | TCAAAAAAACAAAAA[A/T]AAAAACAAAAACAAA | 84669 |
rs541398933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358924 | TTTAAAATGTTATAA[C/T]ACACAATAAATTGAT | 84669 |
rs541432131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231274 | TCAATTAACAGTTAT[A/G]TCAATTTCATATTTC | 84669 |
rs541453238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375863 | TCTGCCTGTCTCAGC[A/C]TCCCAAAGTGCTCGG | 84669 |
rs541461368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60260933 | AACTGCAAGCTCTGC[C/T]ACATCATGTATCTCA | 84669 |
rs541468000 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60279270 | TTTGGGAGTCTGTGG[C/T]AGGGGAGGATTGATA | 84669 |
rs541473023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60285269 | GGTTCCCTCAATATT[G/T]TAAGCAAAATAATTT | 84669 |
rs541488300 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60391778 | TTCCCTTCCGCCTCA[A/G]GCGCCCCACGCCCTC | 84669 |
rs541491900 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60188931 | GGTATCCTAAGTGCA[A/T]CACTGAAAGTGGAAG | 84669 |
rs541501073 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422032 | CAGCACCCAGCACCC[A/G]GCACGGAGGGCTTAT | 84669 |
rs541521928 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60371568 | GCAAGATTCTGTCTC[-/A]AAAAAAAAAAAAAAT | 84669 |
rs541548556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60342362 | CTCAGAAGTGTTTCC[C/G]AGTTAGGCTACACAG | 84669 |
rs541564739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407153 | CAATCTCACTGAGGA[C/T]GCACAGATTGGAGTT | 84669 |
rs541570355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237063 | TCCCATCAGCAATTC[C/T]AGTGGGTGTGAAACA | 84669 |
rs541578427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244588 | TCTTAGAGATTGTTG[C/T]AGGGTTTACAATATG | 84669 |
rs541584284 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403978 | CTTGGGAGTCAAGGC[C/T]GCAGTGAGCCGCGAT | 84669 |
rs541611413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60267059 | CTCCCAAAGTGGTAC[A/G]ATTACAGGCATGATG | 84669 |
rs541621625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60275096 | ATGTTTTGTTCCCTG[G/T]TACAGTCTAACACCA | 84669 |
rs541625418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358880 | TGTCACTTGCCAAGA[C/T]TGAGAATCTCTGGCT | 84669 |
rs541641323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243690 | TTGCAGATTGTACAG[A/C]ATCAGGCAGTGGGAC | 84669 |
rs541676254 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60230247 | TAATATTTGGAATTG[G/T]ATCTTAAATGTTTTA | 84669 |
rs541676946 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60390623 | CAATTCTGTATCTTA[C/T]TGTCAGGTGATGGTC | 84669 |
rs541679765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60208229 | GTAAAGAGAAAAGAT[A/C]TTTTATTGGTAAAAT | 84669 |
rs541716762 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60346707 | TCACAATAGAGGCAC[-/A]GAAATGGTACCTTTG | 84669 |
rs541723598 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60308697 | CTTTGGGAGGCTGAG[A/G]CAAGTGGATCACTTG | 84669 |
rs541737563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229400 | ATGCAGCCAGAATTA[A/G]TAACTATTGCCCTAG | 84669 |
rs541745524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60340668 | CATTTAGCCCATTTA[C/T]ATTTAAGGTTAATAT | 84669 |
rs541760641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60316481 | CAGTGAGCACGTTTC[C/T]GCAGTTCAACTAGTA | 84669 |
rs541760893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60358167 | ATTGCAAATATAGAG[C/T]ATTTCAGCTATACTA | 84669 |
rs541771290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60366227 | GCAGTGGCGCGATCT[C/T]GGCTCACTGAAACCT | 84669 |
rs541820794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60275894 | TTTTTTGTATTTTTA[A/G]TAGAGACCTTGTCTC | 84669 |
rs541822251 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60386446 | TCTCAGCATTACTCT[A/G]GTGCTGCAAAAACAG | 84669 |
rs541844419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375120 | TTAAATAAGTTTTAC[A/G]AAAGTGCTGTTGGTG | 84669 |
rs541852987 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60353231 | CACAGAGGAAAGAGC[A/G]TGTATGGATGCAACG | 84669 |
rs541857451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60215022 | TGCCAGACTAGAGTG[C/T]GGTGCTGTGATTTTG | 84669 |
rs541878165 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306643 | ACTCCGTCTCGAAAG[-/A]AAAAAAAAATGTCTT | 84669 |
rs541884080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60284365 | ACTACAGGGGTCTGC[C/G]ACCATGGTTGGCTAA | 84669 |
rs541890470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60230526 | GCGGTTCTACCACAT[G/T]CTTTTAACATGGTAC | 84669 |
rs541914593 | snp | A/C/G | 0.00239393 | 0.0345281 | intron-variant | USP32 | GRCh38.p7 | 17:60214533 | AAAATTGGAACAATA[A/C/G]AAAGAAGTTTAGCAA | 84669 |
rs541914721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60399857 | CAGCAAGGAAGCAAG[C/T]GTGCCTGCAACAGTG | 84669 |
rs541937117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60323903 | AAGAAATTCTTCTTC[A/G]AAGATGGAATACTAG | 84669 |
rs541956855 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222266 | TGAAGGAACTTAACA[A/T]TGAACAATCCACACA | 84669 |
rs541967698 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60398826 | CTACAAAAAAAAAAA[A/T]TTTAATTAGCTGGGT | 84669 |
rs542025011 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | USP32 | GRCh38.p7 | 17:60183244 | TTCCCCAGCCGAACT[C/G]TGCGCATCCACTTTC | 84669 |
rs542030025 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60292097 | ACTAGACCTTCCAGG[G/T]TATTTGACATAGTTG | 84669 |
rs542051752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406282 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 84669 |
rs542075496 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60200113 | GCAGGAGAATCACTT[A/G]AACGCAGGAGGCATA | 84669 |
rs542088093 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60190864 | AATAATTAGTACAGT[A/T]TCAGGGAATCATGCT | 84669 |
rs542088161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60182646 | TGCATGCCTGTAGTC[C/T]CAGCTACTCAGGAGG | 84669 |
rs542093334 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60300720 | AAAATTCACCCTTTT[A/C]AAATAAACATTTCAG | 84669 |
rs542100357 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60244470 | TCTATTTGTTCCTCT[A/G]TTCCTCTAGTTCTTT | 84669 |
rs542123934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413447 | GGCTAAGTCATAAAC[C/T]AGTACAGGGAGGCTA | 84669 |
rs542136579 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60247324 | AGCTGGGATTACAGG[C/T]GCCTGCCACCATACC | 84669 |
rs542137603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60252508 | ATTATCTGCATGAGA[A/C]CCATTTCCTAAATTG | 84669 |
rs542163751 | snp | A/G | 0.00277227 | 0.0371275 | synonymous-codon | USP32 | GRCh38.p7 | 17:60301657 | TCCAACTATTAAATT[A/G]TTGAAGTGCAGCCCT | 84669 |
rs542202078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362277 | ATGTGAAGAAAAATA[C/T]AGAATGAAATCTGTA | 84669 |
rs542215068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256717 | TCAATGCCTGCACCA[A/C]GGCAACAGAAGAACT | 84669 |
rs542232657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60374102 | GGCAAGAGAATCGCT[G/T]GAACCAGGGAGGCGG | 84669 |
rs542247237 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60316059 | TGGGACTTCAAAACA[G/T]ATCTGTGCTTCCAGA | 84669 |
rs542248028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60266978 | ATTTTTAGTAGAGAC[A/G]GGATTTCACCATGTT | 84669 |
rs542248758 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60368702 | TGTTTCTACTGCACA[C/T]AGTAAGCACTTCACA | 84669 |
rs542269831 | in-del | -/ATTA | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423864 | TTAGATGCATGGTTT[-/ATTA]GTCCATTTTGCATTC | 84669 |
rs542272174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369828 | CTGCAGACTTGAACT[C/G]CCTGGCTCAAGTGAT | 84669 |
rs542310932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378821 | GGATGATGAACAAGT[C/T]CTGGAAATGGATAGT | 84669 |
rs542311781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211317 | AAGAGGAAATTTAGG[G/T]GATATTGGGTTTATA | 84669 |
rs542330447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60319650 | GCAGAAGTGGTGGTG[C/T]GCACCTGTAGTCCCA | 84669 |
rs542330525 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60328883 | GCAGCAGCCAGTGTG[C/T]CTTGACTGCACACTG | 84669 |
rs542341021 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60212160 | TACCCATTCGATTGC[-/T]TTTTTTTTTTTAAAG | 84669 |
rs542367259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60328042 | CAGGCAGCAGACAGG[C/T]TCCTGGGCAGAAGGG | 84669 |
rs542376096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60279090 | ACATAGAATGTTTAT[A/G]CTCCCTATACAAGCT | 84669 |
rs542376741 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60266490 | GAGTTGTTTCTTGTT[C/T]TTCTTTTTGTTTGTT | 84669 |
rs542379941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228862 | TGGTAGAAATGGAGT[C/T]TTACTGTATTGCCCA | 84669 |
rs542419041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60282479 | CTGCCTCAGCGTCCA[A/G]GGTAGCTGGGACTAC | 84669 |
rs542423298 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60398557 | TCATGCCTATTTAAC[A/G]TCTTCCCACTACCCT | 84669 |
rs542438419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274208 | CAGCCAATTATAAAC[C/T]AGACAGGAAAGATTA | 84669 |
rs542440101 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60390590 | TATTCTGGTAAATCC[A/C]CCACCACCAATACAT | 84669 |
rs542454947 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179203 | GCCAAATGTCAGCTA[C/T]AAGGAGTCATCTCCC | 84669 |
rs542479606 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295336 | AAATATGTGTTTCAA[C/G]ATGGATAAATATCAA | 84669 |
rs542481475 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60260510 | CCTGGGTGACAAGAG[A/C]AAGACTTTAAAAAAA | 84669 |
rs542482373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60289842 | TCTAATCCTAATAGA[C/T]ATGCTAAAGAATACG | 84669 |
rs542485571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60187302 | AGGCTAAAGAGCTCA[C/T]TTAAAAAGGGGAACT | 84669 |
rs542509002 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60181165 | AGGTGTGAGTCACCA[C/T]ACCTGGGCAGGCCAA | 84669 |
rs542514762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404630 | GGCATCTTGAAGCTA[C/T]GTATGGTTTATAGGG | 84669 |
rs542525850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235345 | CATTTGCCTACTTTT[C/T]ATTCCTTCAGAGACA | 84669 |
rs542527199 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210587 | GCTGAGATTACAGGC[A/G/T]TGAGCCCCTGCGCCC | 84669 |
rs542529915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60287039 | CCTATAATCCCAGCT[A/G]CTCAGGAGGCTGAGG | 84669 |
rs542535479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348015 | TAGTCCCAGCTACTT[G/T]GGAGGCTGAGGCAGG | 84669 |
rs542563017 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60401781 | ATGAACTTCAGCCTG[C/G]TTGTCACTCAGAGAT | 84669 |
rs542583155 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60344458 | TTATAAAATTTATTC[A/T]TTTTTTCTTTTGAGA | 84669 |
rs542584694 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60371244 | GGGGAAGACTCTGTC[G/T]CTAAAAATTAAAAAA | 84669 |
rs542595857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417372 | GCTGGTCTCTAACTC[C/T]TAGGCTCAAAAGATC | 84669 |
rs542596621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186862 | AACAATCAAGAATCA[C/T]AGAGCCGGGATCCTT | 84669 |
rs542659733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60294146 | CCTGGGCTCAAGAGA[G/T]CTTCTCACCTGGGTC | 84669 |
rs542665466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60263997 | CCAATTTATGCAAAT[A/G]TGTCTCATACAGGTA | 84669 |
rs542691157 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60190126 | TTAGTTTCCAAGAGA[C/G]CGGGCTGTTAGAAAG | 84669 |
rs542692435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416084 | ACCTCATGATCTGCC[C/T]GCGTCGGCCTCCCAA | 84669 |
rs542703538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60219230 | CAAAAAAGATGATAG[C/T]ATAAGAGGAATTGCT | 84669 |
rs542703773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194583 | CTCCACCATTTCTCC[C/T]GTTATTATTCTTGGT | 84669 |
rs542727465 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415223 | AGGGCTGGATGTAGG[C/T]TGCTGGCAGGGAAGA | 84669 |
rs542738453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60246606 | TATTTTTAGTTTATT[G/T]GGGCACCTCCATACT | 84669 |
rs542759218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60310428 | AAAAGAGGCTGGGTG[C/T]GGTGGTTCACGCCTG | 84669 |
rs542772359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60262338 | CTGGAATTACAGATG[C/T]CCAACACCATGCCCG | 84669 |
rs542785148 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60242966 | TAGAACAATTTGAGA[A/C]AATTGCCATATTGAC | 84669 |
rs542817647 | in-del | -/AA | 0.00729562 | 0.0599549 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404040 | GCGAGACCCTGCCTC[-/AA]AAAAAAAAAAAAAGG | 84669 |
rs542831249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387202 | GTAGTATAAATCTAA[C/T]GAAATTTTAAGATTA | 84669 |
rs542833888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261903 | CCAAAAGGAAAGAAA[C/T]GTCATGAAAAGAAAT | 84669 |
rs542834109 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60394738 | TGTAGGTAATTTTTT[A/T]TTTATTTATTTATTT | 84669 |
rs542835710 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60268833 | CCCAAAATATGCAAC[A/T]TTTGGGAAGATTTAT | 84669 |
rs542843468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60270218 | GATACATCAATCCCA[A/G]TTCTAAAAAGGTAAA | 84669 |
rs542852623 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230736 | CTTCCCCTTCCTACA[C/T]GCTTATTTTTCTTGT | 84669 |
rs542865581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60377127 | ATATGCCCATTAAGA[C/T]AGGATATCTTCTGAG | 84669 |
rs542869802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60386096 | AAAAGCTAGTTTTTA[C/T]CAGGCTTTTGTGCCA | 84669 |
rs542881941 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60303940 | AGATCATATCAATGA[C/T]GTAACATTCAAGTAA | 84669 |
rs542903293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422836 | CTGGCGAGATGATGG[A/G]GAAGAGGTCGCCTCT | 84669 |
rs542906600 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394066 | GCTGCCCTTTCCAGT[G/T]CACTGTGAGGTGGTT | 84669 |
rs542909852 | snp | C/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422228 | ACACGTGCAGGAAAA[C/T]GAGTTCAACAGCCTT | 84669 |
rs542925227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232658 | TTCGAGCTATTCTTG[C/T]GTCTCAGCCTCCTGA | 84669 |
rs542947840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232044 | CTACCCTCACAATTA[A/G]TAATATTCGTAAGTA | 84669 |
rs542947947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268224 | CTTCCATTAGTTCAT[C/T]AGCAAAAAAAGAAAT | 84669 |
rs542957578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223209 | TAAGAATAACAATAA[C/T]GCCAAGGGTTACTAA | 84669 |
rs542963140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60247426 | CTCAGGTGATCCAGC[C/T]GTCTCGGCCTCCCAA | 84669 |
rs542981256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60343602 | TGTTCTTTGAAACCA[A/G]TGAGAACAAAGACAC | 84669 |
rs543007069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60353007 | AGGGGAGAATTTGAA[C/T]ATATTACATTGTATT | 84669 |
rs543011785 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373506 | TAGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 84669 |
rs543043841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360996 | TAGCCAGGTGTGGTG[G/T]CACATGCCTGTAATT | 84669 |
rs543043899 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60293270 | TCCATCTACAAAAAT[A/G]AGAATGTCTGCATAA | 84669 |
rs543045116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263283 | GATCACACTTGTCTA[A/T]CTTTACCTGTATACT | 84669 |
rs543048443 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60218560 | TAATAACATGCTGGT[A/G]TTGTTAACATAGTCT | 84669 |
rs543055831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60352235 | CTCCATGAAGGCTTC[C/T]TAAAAGGTAACAGCT | 84669 |
rs543068131 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407959 | AAAAATCAGCTGGGC[A/G]TGGGGGTGAGCGCCT | 84669 |
rs543073114 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60369270 | AAGTGCTGGGATTAC[A/C]GGCGTGAGCCACCGC | 84669 |
rs543073972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378180 | CATACAAATGACCAA[C/T]AGCACATTAAAAAAA | 84669 |
rs543090263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60319401 | CTTGCCACAACAAAA[A/C]TTTTAAAACATAGTA | 84669 |
rs543111704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218050 | CCTCACTGTTCTTTG[A/G]TTTTGCTGTTTTCCC | 84669 |
rs543112796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60386001 | CTATAAAAGAAAATT[A/C]TATTCTATTGCTGCA | 84669 |
rs543113614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225268 | GACCAGCCTGGGCAA[A/C]ATGGCAAAACCCTAT | 84669 |
rs543123855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60224235 | CATCACTTTGTAACC[C/T]TCTGCCTGTGGTATG | 84669 |
rs543149727 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60236424 | CAATTTCAAGAGTCA[C/T]AGGGCAGTATCAAGA | 84669 |
rs543150440 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60216787 | CAGAACAAAACCCAA[-/C]CCGTGATCAGTTTTT | 84669 |
rs543162998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60254370 | AGGAAACAGCCTCAT[A/G]CCTTCAATGATCTCT | 84669 |
rs543166419 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60344330 | AAATGGTGTTTTACC[A/G]TGTTGGCCAGGCTGG | 84669 |
rs543168228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60195135 | TCTTTTTTAATGTCC[A/G]AAGGACATAACCCAC | 84669 |
rs543168255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60335011 | ATTTTTTAAGAGACA[C/G]GGTCTCTATTGCCCA | 84669 |
rs543184453 | in-del | -/GAGCATGCCCAGATGAAGC | 0.00358779 | 0.0422022 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408756 | AAGGTTATGTAACCT[-/GAGCATGCCCAGATGAAGC]GAGCATGCCCAGATG | 84669 |
rs543218173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186405 | AAACCAGAGCTGGAT[A/G]AAATAAGGGCACAGA | 84669 |
rs543227085 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231876 | AGCGGGGAAAGACTG[G/T]TAAGATTCCATGAGC | 84669 |
rs543246337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60309770 | AAGCAGGCAGACTGG[A/G]CACAGTGGCACATAC | 84669 |
rs543277114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60332870 | TTGTTGCATATACCA[A/G]TAGAGCTTCCTTTTT | 84669 |
rs543279865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60209613 | GAACATGTCCTATAA[C/T]CCAATCAGAGCCATT | 84669 |
rs543282649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194535 | TCTTCTTTACTCACT[A/G]AAGATTGCAGCACCC | 84669 |
rs543288037 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60268191 | CTATTTAACTCCAAA[C/T]GAATCATTCTAGTTT | 84669 |
rs543290423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286485 | CACCAAAAAATGGAA[A/G]AGGCAAGGAATAATT | 84669 |
rs543305537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60343538 | AAATTGAACAACCTG[C/T]TCCTGAATGACTACT | 84669 |
rs543313911 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60300961 | TATGGCCTATTGGGA[C/T]TGACATCTATCACTA | 84669 |
rs543328112 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232838 | AGGCGTGAGCCACCA[G/T]GCCTGGCATGAAAGA | 84669 |
rs543335749 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60266932 | GTGCTGGGATTACAG[A/G]CGTGAGCCACTGTGC | 84669 |
rs543337723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60238560 | ATAATCCCAGCACTT[C/T]GGGAGACCGAGGCAG | 84669 |
rs543355378 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413219 | CTGTATCCTGCCAGT[A/C/G/T]GGGGAGGGAAAGACC | 84669 |
rs543380498 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60352184 | CCTTGCAACTAGAAA[C/T]GGCCAATGAAATGCA | 84669 |
rs543387184 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60260488 | AAATCACGCTATTAC[A/G]CTCCAGCCTGGGTGA | 84669 |
rs543393116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60193746 | CTATTGAAGGTAATG[A/G]AACCATGATAAAGAG | 84669 |
rs543398051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424425 | TTCTCATCTGTAACT[A/G]GGGTTAATGATATTG | 84669 |
rs543419266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360459 | AAGTCAGGAGTTCGA[C/G]ACCAGCCTGGCAAAC | 84669 |
rs543442950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60270024 | CTTTCATAAAGCAAA[A/G]GAAGATACACTATGC | 84669 |
rs543460739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301806 | TCCACCTCCACAACA[G/T]GCCCTGGTAAATTTT | 84669 |
rs543467242 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60267724 | CAGGGTTTCACCATA[C/T]TGGCCAGGCTGATCT | 84669 |
rs543494370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201185 | GTTTGGCTTCTTTCC[A/G]TCAACATTAGGTTTA | 84669 |
rs543496396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415156 | TTGCAGCCTGTCTTG[A/G]AAGGTCCTGATGCCT | 84669 |
rs543504996 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60273378 | ACACATTGTTGGACA[C/T]TGGGAGCATTTGTGA | 84669 |
rs543507129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60269094 | CAGTGGATGGAAAAT[A/G]AGTTATGCCTCAACT | 84669 |
rs543516234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232544 | CTGGAAAGAGAAATT[C/T]GATTTTTTTTTTTTT | 84669 |
rs543518550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327196 | TAATGGCCATGTGTA[A/G]TGGCCTATTTGACAT | 84669 |
rs543524798 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179038 | TGGTGGGATCTGCCT[C/G]AAAGTTCTCTATCGG | 84669 |
rs543549275 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403169 | GGCGCGCGCCACCAC[A/G]CCCAGCTAATTTTTG | 84669 |
rs543579993 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60286958 | TTTGAAACCAGCCTG[A/G]CCAACATGGTGAAAC | 84669 |
rs543614831 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60374097 | GCTGAGGCAAGAGAA[A/T]CGCTTGAACCAGGGA | 84669 |
rs543617321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60278087 | AATTTTCAAATTTTT[C/T]GTAGAGACGGGCCTT | 84669 |
rs543643052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60268008 | CCGAGACTATGTTTC[A/G]CCATGTTGGCCAGGC | 84669 |
rs543670974 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60275844 | AGCCTCCTGAGTAGC[A/T]GGGATTACAGGCACC | 84669 |
rs543674449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401692 | TTGAGACCAGCCTGG[A/C]CAACATGGTGAAACC | 84669 |
rs543723562 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60200398 | AAACTCTGTCTCTAC[C/T]AAAAATACAAAATTA | 84669 |
rs543745385 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60316065 | TTCAAAACAGATCTG[A/T]GCTTCCAGAATACAG | 84669 |
rs543766258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60351519 | CTGCAACCTCTGTCT[C/T]CCGGGTTCAAGCAAT | 84669 |
rs543771877 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306447 | GTTCGAGAGCTGCCT[C/G]GCCAATGTGGTAAAA | 84669 |
rs543778549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201535 | CTCATCAGCATGGTA[A/T]GAGAGTTCCTGTTGC | 84669 |
rs543787739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190418 | GCTCAAGCAAACATG[C/T]CAATATATTAGGTGC | 84669 |
rs543791575 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60207818 | TAGAACACTCCATAT[A/T]GGCAGCCTTACGTAT | 84669 |
rs543792073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298690 | CTGGGGCCAATTTAT[A/G]TTTCTGCTGGTGAAG | 84669 |
rs543816674 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378274 | TAGGATGGTTATTAA[C/T]TGAAAGAAAACAAAA | 84669 |
rs543825445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347391 | CGGCATCTTGCTCTG[C/T]CGCCCAGGCAGGAGT | 84669 |
rs543847109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60198596 | ATAAAACCATCTTTA[C/T]TGACACAAAGAGAAC | 84669 |
rs543852388 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298065 | CTTATAGGGCCTAAC[A/T]GTAATGCATTTAAAT | 84669 |
rs543852992 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60254227 | TTTAAAAATCAGAGC[A/G]AGGGAATTAGTTTAA | 84669 |
rs543867848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306395 | GTAATCCCAGCACTT[C/T]GGAAAGCCGAGGGGG | 84669 |
rs543884171 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419571 | CCCCGTCTCTACTAG[A/G]AATACAAAAAAATTA | 84669 |
rs543913265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60208572 | TTTATTTGTAAACAA[A/G]TAACTATGCTTACAA | 84669 |
rs543914260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403979 | TTGGGAGTCAAGGCC[A/G]CAGTGAGCCGCGATC | 84669 |
rs543919991 | in-del | -/CTTTCT | | | intron-variant | USP32 | GRCh38.p7 | 17:60239671 | TGGTTCCTTTTTATA[-/CTTTCT]CTTTATTGATACTCT | 84669 |
rs543948867 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60203821 | ACCTCACGATCCACC[C/T]GCTTCGGCCTCCCAA | 84669 |
rs543948897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216846 | TCAGCAAGCAAAGGA[A/T]AATCTCTAAAAGAAA | 84669 |
rs543957325 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60316670 | ACATGGTGAAATCCC[A/G]TCTCTACTAAAAATA | 84669 |
rs543993055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204813 | AGACAGGGTCTTGCC[C/T]AGCCTGGAATGTGTG | 84669 |
rs543994673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265538 | TAATTTTGTTATTCA[A/G]TGGCTAAAGTATATT | 84669 |
rs544004388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60272901 | TGAGTTTTGGCAGAA[C/T]AGTAAGCTGTGTATA | 84669 |
rs544024883 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60287377 | CAATGAGTATCCTCC[A/G]TGTATTGATTTACGA | 84669 |
rs544050577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375339 | TAGTCTCAGCTTGCA[C/T]GGTCATTTTTACAGT | 84669 |
rs544055837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60383674 | ACATGTAAAAATTCA[C/T]AAATAGTCTTTCCAG | 84669 |
rs544056692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223165 | ACATAGCGTATGTGA[A/T]ACAACATTTTCAGAA | 84669 |
rs544058343 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60215953 | AATCCTCCCACCTTG[G/T]CCCCCCAAAGTTCTG | 84669 |
rs544061517 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233148 | AATAATAGCTACCTA[C/T]TTAGTACTTACTATG | 84669 |
rs544061651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388626 | TCCTTAGAAAACACA[C/T]GCAATATAAACAAGA | 84669 |
rs544065834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271874 | TGGAGTGCAGTGACA[C/T]GATCATAGTTCCCTA | 84669 |
rs544067508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257490 | GTTGTTATTTATTTT[A/G]TTTTGTTTTCTAAAA | 84669 |
rs544072144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325837 | GGGAGGCTGAGGCAG[A/G]AAGATTGCTTGAGCC | 84669 |
rs544081437 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264687 | CATAACGAAACCCCA[A/T]CTCTACTCTAAAAAT | 84669 |
rs544107904 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60272957 | GCTATGTACAAATGC[C/T]GGGAAATTTGTTTTG | 84669 |
rs544117961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60313482 | TGCTTAGCTCCAAAA[A/C]AAATAAAGGGCCCCT | 84669 |
rs544124862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60334150 | ACTGTAAAAAAGCAA[C/T]AAGAGGTGGCCATGC | 84669 |
rs544140344 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60380182 | CCTTTCCAACACATT[G/T]TACAATACAAAATTA | 84669 |
rs544167227 | in-del | -/ATTTT | 0.314337 | 0.24158 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420088 | ATTTTATTTTATTTT[-/ATTTT]ATTTGTTTTGTTTTA | 84669 |
rs544178635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280939 | CTTTGTGATAATGCT[G/T]TTCATAGTAAGACTC | 84669 |
rs544182256 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60241894 | GTCTTACACTTTTTT[C/T]CCCACTTATAAACTG | 84669 |
rs544187656 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60285719 | AATGAGAGATAATTT[C/G]TGATAAGAAGGCAAG | 84669 |
rs544197199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387963 | CCATCGTAAAGTTAA[A/C]TTGTAAGTCGGGGAT | 84669 |
rs544228928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60364888 | TACAAGTCAAACCTT[A/G]TATTTTAGACCCAAA | 84669 |
rs544228933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356397 | AATTCCCATATCTCT[C/G]ACTTTGGCTGACCTT | 84669 |
rs544233580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60395565 | TGAAGTCTGCTTGTC[A/T]TGCTGAAAGGAATTC | 84669 |
rs544246279 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60390741 | TCTAATTACCATTTT[A/C]TATCCTTAGCTACTA | 84669 |
rs544248684 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60364908 | TTAGACCCAAATTTT[A/G]TATTTGTAAAGAAAG | 84669 |
rs544252974 | snp | C/T | 1.70165e-05 | 0.00291684 | intron-variant | USP32 | GRCh38.p7 | 17:60226238 | GTTGGCATCCTAAAA[C/T]CAGGAAATCAGAGAA | 84669 |
rs544277011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60240838 | TTAAAATATTTTACC[C/T]CAGGTGACTGCAGGT | 84669 |
rs544287266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60180445 | TTCTAACAGAAATAT[A/C]TATTTCCTATTCAAG | 84669 |
rs544307039 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256449 | TTTTTTTTCCACCCA[A/T]ATCAGTACAGCAGAG | 84669 |
rs544331038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60287888 | GGAGGCCGAGGCGTG[C/T]GGATCACGAGGTCAG | 84669 |
rs544347822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60213289 | GAAAATTTTAAGGAA[C/T]TATAAATGTGTAAAC | 84669 |
rs544351094 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60292232 | GAGTCCTCTTCATCT[C/T]TCCAAACTCTAAACA | 84669 |
rs544354306 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60248296 | CTTGTGGCTTTCAAC[G/T]TCTTCCTTTGTCTTT | 84669 |
rs544355857 | in-del | -/A | 0.0547245 | 0.156101 | intron-variant | USP32 | GRCh38.p7 | 17:60240495 | AAAGAGAAAAAAGGG[-/A]GAGAGAGAGAGAGAG | 84669 |
rs544380595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60372319 | ATGACAGGAATGCAT[C/T]GTTAGGTGATTTCAT | 84669 |
rs544380748 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60346619 | GAAAACTTTTTTTCA[C/T]TATATGGAACAATCT | 84669 |
rs544409921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60345165 | AAAACATATTTGCAA[A/C]ATAAAAATTTTTATG | 84669 |
rs544419296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60247536 | ATTGGGAACTGGTTT[A/C]ATTCTTCTGCACGTG | 84669 |
rs544420075 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60380792 | TTGAGAGAAATGTCT[C/T]AGAACCAGTCAAACC | 84669 |
rs544433554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60322520 | ATAGATTGTAATAAA[C/T]AGATGTAATTTCAGA | 84669 |
rs544442442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60371463 | AATCCCAGCTACTCA[G/T]GAAGCTGAGGCAGGA | 84669 |
rs544445623 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60354060 | CATGTGTGAAATGCA[G/T]GAAATTAAATCCATT | 84669 |
rs544456449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60220891 | CTGACTTCGTGATCC[A/G]CCCGCCTCAGCCTCC | 84669 |
rs544476697 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60338513 | AGGCAGGGTGATCAC[C/T]TGAGCTCTGGAGTTC | 84669 |
rs544477983 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60221620 | CAGACAATTCTCCTG[C/T]CTCAGCCTACCAAGT | 84669 |
rs544501336 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60317420 | ACTCGGGAGGCTGAG[C/T]TGGGAGGATTACTTG | 84669 |
rs544505176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60226749 | TACATAGAGTGAAGG[A/G]CAATGCTATGACTTA | 84669 |
rs544517978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60220253 | AATTTACACTATTGC[C/G]AGTAATGTGTAAGTA | 84669 |
rs544566585 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60234259 | GCTGGGACCATAGGC[C/G]CCTGCCACCATGCCC | 84669 |
rs544584028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197007 | CCAACATGGTGAAAC[C/T]CTGTCTCTACTAAAA | 84669 |
rs544587069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60181216 | CTATCACTAAGCTCA[A/G]TGCTAGGAAATAAGC | 84669 |
rs544600896 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | USP32 | GRCh38.p7 | 17:60211222 | ATATCTTTTCTTTTT[A/G]AAACAAGAGATGTAT | 84669 |
rs544622229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60189323 | TAAGAAACTAGGTCT[A/T]GAATTGGTAGTTTCC | 84669 |
rs544632083 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60288387 | TGAGACTGCCGTAAG[A/C]CACGATGGTGCCACT | 84669 |
rs544645977 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60355269 | AGAACAGTTATTGCC[A/T]CTGAGGATGTGGTAA | 84669 |
rs544647365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60204657 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCACAT | 84669 |
rs544651164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60314199 | GCTGGAGAATACAGT[A/G]GCATTGATCTTGGCT | 84669 |
rs544659870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60395164 | CCTTTGACTGAAACA[C/T]GACTGTAGCTCATGA | 84669 |
rs544664750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403156 | AGCTGGGTCTACAGG[C/T]GCGCGCCACCACGCC | 84669 |
rs544684542 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60363183 | TTTGAGGCCAGGCGC[A/G]GTGGCTCACACCTGT | 84669 |
rs544685222 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60345989 | TCTGTCTCAAAAAAA[A/T]AAATAAATAAAAAGA | 84669 |
rs544685629 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60188565 | ATCATTTTCAACAAC[C/T]GCATTATATTTTATC | 84669 |
rs544690104 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60313274 | AAATAAAGTAAGATT[A/T]AAAAAATGCAAGCTC | 84669 |
rs544711944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337567 | TTTTTTTAAGTCATA[A/C]AGTCTGCCCATCAAG | 84669 |
rs544721839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355011 | ATAGCGCCACCGCAC[C/T]CCAGCCTGGGCAACA | 84669 |
rs544766888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320650 | TTTTCATCAACATTA[G/T]AATGAAAAACAACAC | 84669 |
rs544789938 | snp | A/G | 1.86597e-05 | 0.00305442 | intron-variant | USP32 | GRCh38.p7 | 17:60212006 | TAATCTCTTTAAAAA[A/G]TAATACTGGAGACTT | 84669 |
rs544807394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256696 | GTTGCTGTGAGGAAA[A/G]GAACATCAATGCCTG | 84669 |
rs544808635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280787 | TATTATTTGAGTAGA[A/C]GAGCCTGCAAAGACA | 84669 |
rs544848048 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60394706 | AAACCTGTATAGCAT[A/G]TTACTGTACTGAATA | 84669 |
rs544850046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211752 | CTTTTTAATTGCTAT[A/G]ATTTTTCAAAATAAT | 84669 |
rs544856818 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60324643 | CACATTACTTCAACA[A/G]AAATAAAAAATACAT | 84669 |
rs544865461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60264109 | AATAAATGTTACCAA[A/G]CTAAATAAGTCAAGG | 84669 |
rs544879914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271117 | GTCAAACACATTTTA[C/T]ACATGAGCATGCTCG | 84669 |
rs544882870 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60185679 | GGAACAGGAGGAAAG[C/G]GGTGCGTGGGAAGGC | 84669 |
rs544888130 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60397296 | ATACCAGCTCCAGCT[C/G]TGTACCTTTGGCTTT | 84669 |
rs544891043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320544 | ACACCGTTGGGATGA[A/G]GGAAGAAACCGGGGT | 84669 |
rs544900991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60219348 | CAAAGAAATAAAGCA[C/T]GTAAAATCTATTTCT | 84669 |
rs544904192 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60291468 | TAGAAAAAGCTGAGA[C/T]CCATATCACTTAAAT | 84669 |
rs544923063 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60311609 | TGGTGGATCACCTGA[C/G]ATCAGAAGTTAGAAA | 84669 |
rs544933942 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60387247 | GTGAACAAAATCTTA[C/G]TTGGGAGTCAATGTT | 84669 |
rs544949477 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60368721 | AAGCACTTCACAGTT[A/G]TCAGCAATTTCCTAA | 84669 |
rs544972293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249190 | CAGTAACATTCACAC[C/T]CTTTTCCTGATGGAT | 84669 |
rs544974585 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60328965 | ACGCAGTCTCCCTTG[A/G]AGGCATGAGATCCAG | 84669 |
rs544975002 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60256929 | ACACTGACCAACAAC[A/G]TGATTTCATCATTCT | 84669 |
rs544980684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257912 | TAAGTTGCTTTTTTT[C/T]GTAGCCTCTATCCTG | 84669 |
rs544982088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60287880 | GCACTTCGGGAGGCC[A/G]AGGCGTGTGGATCAC | 84669 |
rs545006016 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60376067 | TTTTGTTTTTAGAGA[C/T]GGGGTCTCACTCCTG | 84669 |
rs545007969 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60399501 | TCTACAAAAAAATTT[-/A]AAAAAAAAAAATTTA | 84669 |
rs545036974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257334 | GTGGATCACATGTGC[C/T]AATTGGGGGGAGTCA | 84669 |
rs545038351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212643 | CTTGAAGTAAAATTA[C/T]ACTCAACCATCTACA | 84669 |
rs545040906 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60287128 | GCACTCCAGCCTGGG[C/T]GACACAGCAATACTT | 84669 |
rs545069440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60394805 | CTGGAATGCAGTGGC[A/G]CAATCTCGGTTCACT | 84669 |
rs545074618 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60226547 | TTTTTTTCTTTTCTT[C/T]CTTATTTCCCATAGT | 84669 |
rs545101205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60220098 | TACTACCCTCACACC[A/G]TAAGTCTTTTCATTT | 84669 |
rs545115517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264582 | GATGTACTGGCCAGG[C/T]GCAGTGGCTCACGCC | 84669 |
rs545135524 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312200 | GAAATACTATCTCAG[G/T]ACAGAAGGCGGAAAC | 84669 |
rs545156898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60255644 | TTACTTTCCTAACTC[C/T]CCTACAATGCAGAAG | 84669 |
rs545169330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60371394 | CAATGTGGTGAAACC[C/T]CGTCTCTACTAAAAA | 84669 |
rs545180092 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60303447 | GAGAATGTCTTTGAG[G/T]TGTGATAACAAATAG | 84669 |
rs545183273 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60344663 | GGTCTCACTATGCCC[-/A]AGGCTGGCCTGGAAC | 84669 |
rs545209342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387930 | TATGATTTCTACTGA[A/T]CGCATATAGCTTCTG | 84669 |
rs545221161 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60247464 | GGATTACAGGCATGA[G/T]CCACCTCGCCCAGCC | 84669 |
rs545247969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60395274 | TGGCATCCCCTAAGG[A/T]CATAAAAATTTCCAC | 84669 |
rs545252831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378134 | ATTCAAAAATGGGCA[A/G]AGGATTGAATAGACA | 84669 |
rs545253933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60361249 | GCCCATTCAGTCTTC[C/T]CCAAGAGATAATCAG | 84669 |
rs545312718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60180172 | CTGGGATTAGAGGCA[C/T]GCGCCAACACGCCCA | 84669 |
rs545313365 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | USP32 | GRCh38.p7 | 17:60226220 | TGGCTCAATTACCAC[A/G]GGGTTGGCATCCTAA | 84669 |
rs545323494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233535 | GTAACACTATGAGGG[A/C]GATTATTATTATTAC | 84669 |
rs545324027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416118 | GCTGGGATTACAGGT[A/G]TGACCCACTGCGCCT | 84669 |
rs545328876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60262389 | TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGC | 84669 |
rs545359164 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60240015 | GCTGGGATTACAGGC[A/G]TGGGCCACCATGCCC | 84669 |
rs545362784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424249 | CATGAGATTTAGAGG[A/G]GACACACATTCAAAC | 84669 |
rs545371407 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60299933 | TCTCTCTGGGGCCTC[C/T]TTTATTAGGGCACTT | 84669 |
rs545390285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60344967 | TGGCGCCGGTTAAAC[A/T]TATTATTTTTAGAAA | 84669 |
rs545394878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353915 | TCTAAACTTTTAGAG[C/G]TTACCGTGTCTACAC | 84669 |
rs545395979 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | USP32 | GRCh38.p7 | 17:60217876 | TTGAGTAGCTGAGAC[C/T]ACAGGGCACACCACT | 84669 |
rs545426093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60399760 | CCAAAATTGGAAGGA[C/G]AGAATGAAGCAGACT | 84669 |
rs545427512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296079 | ACAGAATGGGATCAT[A/G]AAGGGATACAAAGAA | 84669 |
rs545429056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60344563 | CAAGCAATCCTCCTA[C/G]TTCAGCCTCCTGAGT | 84669 |
rs545432467 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60283701 | AATACCTTTAGGTGG[A/C]TCATGGCAGGGAAAG | 84669 |
rs545433157 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233021 | ATTAATCTCATTGTT[C/G]ATATGTGAAAACTGA | 84669 |
rs545441903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60244832 | AGACGAGGTTTTGCC[A/G]TGTTGGCCAGGCTGG | 84669 |
rs545455883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60236905 | GTGGTTCATCTATTA[C/T]TGTGGCAGACATCAG | 84669 |
rs545462659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60399039 | ATACAGGATGTTATG[A/G]GAACCTAGAGTAGGG | 84669 |
rs545462771 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406203 | TCTGAAAAAAAAAAT[G/T]TTTTTTTGGAGACAG | 84669 |
rs545469376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60247943 | CCTACCTCAGCCTCC[A/C]AAAGCACTAGGATTA | 84669 |
rs545473849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185012 | AGTGCACTGGTGTGC[C/T]TGTGTACACACACTC | 84669 |
rs545478721 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60247786 | CCTCCCCAGTTCAAG[C/T]GATTCTCCTGCCTCA | 84669 |
rs545484630 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60299986 | TGATTAACCCTCATG[A/C]CCTAATCACCTCCCA | 84669 |
rs545495655 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417071 | TACAGGTATGCACCA[A/C]CACACCCAGTTAATT | 84669 |
rs545500569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405656 | AGTCCCAGCTGCTCA[A/G]GAGGCTAAGGTGGGA | 84669 |
rs545520588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60292027 | ACCTACACCAATGAC[C/G]TACCTGCAGATCACC | 84669 |
rs545530641 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60247641 | AAAAAAGAGTTGGTT[A/G]TAAATGTGGGGGGTT | 84669 |
rs545533146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243636 | TTATCCCCTTTTGGT[C/T]TTTTCTAAGCCACTT | 84669 |
rs545543752 | snp | G/T | 0.000399281 | 0.0141238 | missense | USP32 | GRCh38.p7 | 17:60252391 | TTTACCTAATAATTT[G/T]TCCTTCTTCTTCCGG | 84669 |
rs545588191 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413283 | CCTGGCCCAGCAAAA[A/G]GAATGCTGATGTCAG | 84669 |
rs545592053 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60282403 | TCTATTGCCAGACTG[A/G]AGTGCAGTGGTGCAA | 84669 |
rs545593287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60202615 | TTCAGTCTTCTTTAA[C/T]TTCTATCAATATTTT | 84669 |
rs545605498 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328245 | GGATCAGCCAGAGCT[C/G]TACAGATGATGGAAC | 84669 |
rs545606748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60251480 | GCCAGAAGAAACTAC[C/T]GAAAAGTTTGTATGC | 84669 |
rs545610663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358794 | TTCGCAAGGTTTTGA[C/T]ATTACATCATGGGGC | 84669 |
rs545638735 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60368038 | TATAAGAAACATGAG[C/T]ATCCTTGGATTTCAG | 84669 |
rs545638761 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60218362 | CCACTTCAGCCTGGG[C/T]GACAGAGCAAGACTC | 84669 |
rs545656428 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201745 | CCCATTGCAACCTCT[G/T]CCTCTGGGGTTCAAG | 84669 |
rs545662829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60311495 | ATAACATACCAAAAA[C/T]CTACCTCTTGTCTAA | 84669 |
rs545694534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259731 | TTTCATTTTGCAAAT[G/T]TATCCCTTGATTTAA | 84669 |
rs545712151 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60362882 | TCAAAAGGCAGCTAA[C/T]AGTCCAATTTCCTTT | 84669 |
rs545717416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259152 | TTTAGCTCCCTTTAC[A/G]CATTTTATGGTAAGT | 84669 |
rs545718101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60269820 | TACATCATTTTTAAT[A/G]GCTAAAATGACTATT | 84669 |
rs545733007 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60381141 | AGTCCCATTTATTAC[A/G]TCAACATTTTAATAA | 84669 |
rs545733809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60365108 | AATGAAGAAAATGTT[A/C]ATTGTTTTCCAGTCT | 84669 |
rs545735818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60373950 | TACACTTTGGGAGGC[C/T]GAGGTGGGCGTATCA | 84669 |
rs545736161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318407 | CTAGAGAACAGCATG[A/G]GATTAACCATTATGC | 84669 |
rs545754965 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60238708 | ACTTGGGAGGCTGAC[A/G]CAGTAGAATCGCTTG | 84669 |
rs545761535 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60286934 | GGGTGGATCACTTGA[-/G]GTCAGGAGTTTGAAA | 84669 |
rs545770753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60341409 | CTTGTCTGTAAAGGA[C/T]TTTATTTCTCCTTCA | 84669 |
rs545787929 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60184058 | TTGGGAGGCCAAGGC[A/G]GGTGGCTCATGAGGT | 84669 |
rs545798581 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419946 | CTCACTGCAACCTCT[A/G]CCTCCCGAGTTCAAG | 84669 |
rs545804436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60324981 | GCACCCCAGTCTGGG[A/C]AACAAGAGCGAAACT | 84669 |
rs545844668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60354221 | TTTTTTTCAAAGGTA[A/G]TATTTGTCTTATCTC | 84669 |
rs545881551 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60221145 | ATGCCTGTAATACCA[C/G]CACTTTGGGAGGCCA | 84669 |
rs545887165 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60311647 | GGCCAACATGGTGAA[A/G]CCCTGTCTCTACTAA | 84669 |
rs545893703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228019 | GATGGTTCACCAAAG[C/T]AGTCAAAATTCTTTT | 84669 |
rs545898205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60299457 | GCAAGAGGGAGAGAG[A/G]AGGAGGCTGAATTCT | 84669 |
rs545905301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60340748 | GCCCATTAATTGATG[C/T]AGTTTCTTCATAGCA | 84669 |
rs545912551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348695 | ATCACTTGAGCCCGG[A/G]AAGTCAAGGCTGCAG | 84669 |
rs545926353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339447 | AATTAGCCAGGCGTG[G/T]TGGTGGGCACCTGCA | 84669 |
rs545945729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60273008 | GAATCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 84669 |
rs545949478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358021 | TGATCCACCCGCCTC[C/T]ACCTCCTAAAGTGCT | 84669 |
rs545996117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347304 | ATTTGCCTGCCTCAT[A/C]CTCCCAAGTACCTGG | 84669 |
rs546001512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60199477 | TAGTATAATGGAATG[A/G]TTGGTGGGAGTTCAA | 84669 |
rs546007188 | snp | A/C/G | 3.40595e-05 | 0.0041266 | missense | USP32 | GRCh38.p7 | 17:60183170 | CAGGCCTCACCTTTC[A/C/G]GGCTGCTGATGATGT | 84669 |
rs546008468 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60260727 | TATACAGATTTAGGA[A/G]AATTCAGAAAAAAAT | 84669 |
rs546024542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412473 | CTGAGAGGTCAAGGC[C/T]TCAGTGAGCTATGAT | 84669 |
rs546032690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60206308 | GGTGACAGAGTGAGA[A/C]CATTTCTCAAAATAA | 84669 |
rs546051518 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60197793 | TATGAAATTACTTCA[C/T]GTTAAAATGACATGG | 84669 |
rs546069930 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60257099 | AGACAGAAGCCAATA[-/CT]CTCTGATGTTGGGTT | 84669 |
rs546076828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388791 | ACTGACAAACAGTCT[A/G]GCTAAAATAGTGTGC | 84669 |
rs546092112 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60214379 | ATATTACAAGTATAC[A/T]TATAGTAACTTAAAA | 84669 |
rs546097698 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60386833 | ACACACCAAACCTAC[A/G]AACTAAAGATTAGTG | 84669 |
rs546098352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306322 | TATAATTTGTTGCAA[A/G]ACTTTTGTTTTAAAA | 84669 |
rs546105148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306897 | CAACAGTAAACAATC[C/T]AAAAAAGAAATCCCA | 84669 |
rs546144582 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60237096 | TTACACTGGGATTAT[-/A]AAAAAAAAAAATCTA | 84669 |
rs546167516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60266377 | CTGTCAAGAAAGGGC[A/G]AAGTTACTGTACAAT | 84669 |
rs546188903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60182697 | GACCCCAGGAGGTAG[A/G]GGCTGCAGTGAGCTG | 84669 |
rs546195463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297488 | GAGTCTTGCCCTGTC[A/G]CCCAGGTTGGAGTGC | 84669 |
rs546200267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381555 | CACCTCTAGTCATTT[C/T]ACTCAGGTGCTCTTC | 84669 |
rs546205385 | in-del | -/AATT | 0.353835 | 0.227417 | intron-variant | USP32 | GRCh38.p7 | 17:60236516 | CTGGTGTTTCCAATT[-/AATT]AATTAATTAATTACA | 84669 |
rs546236350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60389683 | TCAACTTGCTGCTCT[C/T]TTTTGCTTTAATTTT | 84669 |
rs546263098 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305340 | GAGAGAGGAGGAAGT[A/G]CCAGGCTCCTTTAAA | 84669 |
rs546277215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332006 | CTAGCACTTTGGGAG[A/G]CCAAGGTGGGAGGAT | 84669 |
rs546288540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60282429 | TGCAATCTCGGCTCA[C/G]TGCAACCTCTGCCTC | 84669 |
rs546306570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60288812 | GGAAGGATTATCTAA[C/T]AACACTGCAGGGTGT | 84669 |
rs546342217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190453 | GAGGATGCCAATGAA[G/T]GTTTTTCTGGTTGTT | 84669 |
rs546369141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60182503 | CACAGTGGCTCACAC[A/C]TGTAATCCCAGCACT | 84669 |
rs546369632 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233494 | ACAACAAAACACTTA[A/G]CATGCATCAAACTCA | 84669 |
rs546390787 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60332980 | GTACACAGAACTTAC[A/G]TTTTCAAGATATTTC | 84669 |
rs546397838 | in-del | -/TC | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60216849 | GCAAGCAAAGGATAA[-/TC]TCTAAAAGAAAACAA | 84669 |
rs546398174 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60322834 | CAATTACAAATTTCC[A/G]TATACATATACACCA | 84669 |
rs546420784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60297581 | AGCCTCCCTAGTAGC[C/T]GGGATTACAGTCACA | 84669 |
rs546425817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60242158 | TGTTGTACAGGCTGG[C/T]ATGAGGTGGCTATTC | 84669 |
rs546430692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297978 | AAGAAGACCACTGAC[A/C]ATGGACTGGTTCTGG | 84669 |
rs546451977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60396902 | AATGAAGTTATATTC[A/G]TATCTCCTTCAAATT | 84669 |
rs546454681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197997 | AAGACAGGATATTAC[C/T]TGAAGCATTAGCAGG | 84669 |
rs546456155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404542 | GTTCTAGGAGAAACC[C/G]TCTTTGAGAGAGGAG | 84669 |
rs546463214 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60251377 | ATCTTAATTGGCATG[C/T]CCTGTTTAAATGCTG | 84669 |
rs546474302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410472 | AGGAGATTGAGACCA[C/T]CTTGGCTAACACGGT | 84669 |
rs546487843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410798 | AGAAATAGAAACTGT[C/T]GGCTGGGTGCGGTGG | 84669 |
rs546494966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403725 | ATTTTTTCACACATA[C/T]ATATTTGAAGACTAT | 84669 |
rs546514947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418461 | CTGCATCTTCTCAGA[A/G]TTGTGTTCTGTCACC | 84669 |
rs546518753 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60422428 | TGAGGAAATGGGAGC[G/T]GGGTGGGGGGCTGGG | 84669 |
rs546527111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60257643 | GGTTACCAAAACTGG[C/T]TTAAAAAAAAGAGAA | 84669 |
rs546530503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196801 | CTGCACTCCAGCCTG[A/G]GTGACAGAGCGAGAC | 84669 |
rs546544977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60331348 | AGGCAGGCGGACTGC[C/T]TGAGTCCAGGAGTTC | 84669 |
rs546559469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60273270 | GCATGAGTCACCGCA[C/T]CCAGCCCAGATGCTA | 84669 |
rs546582021 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60339204 | GCATGAGCCACCGCG[A/C]CCAGCCTAGAAGAAC | 84669 |
rs546582443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60288365 | GGACTGCTTGAGCCC[A/G]GGAAGTTGAGACTGC | 84669 |
rs546584776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228168 | TAGCTGGAACTACAG[A/G]CACCTGCCACCACAC | 84669 |
rs546600240 | in-del | -/ATTTT | 0.00346963 | 0.0415063 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420092 | ATTTTATTTTATTTT[-/ATTTT]ATTTGTTTTGTTTTA | 84669 |
rs546600572 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60264214 | AGGAGAGGTCCTTAC[A/C]ACAACCATTTAAAAA | 84669 |
rs546605378 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60382384 | CACCTGTAGTCCCCA[A/C]AATTCGGGAGACCTG | 84669 |
rs546616615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281931 | TAATTCCAATGCTCA[A/G]TATAGCTGGTAACTA | 84669 |
rs546617412 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60380428 | CAAAAATTAGCAGGG[C/T]ATAGTGGTGCACACC | 84669 |
rs546619408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60257288 | ATTGGAAAGTCCTTC[A/G]GCATGCACAGTTATT | 84669 |
rs546634587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312933 | CTACTGATAAAATTT[C/T]AAATGTTAACATTTA | 84669 |
rs546641355 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60247888 | ACGGGGTTTCACCGC[A/G]TTAGCCAGTATGGTC | 84669 |
rs546647179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60397214 | TCAGTTTCTAGATAA[C/T]AATAACTTTGTCAAG | 84669 |
rs546673372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362767 | AAACTTCTGAAGCTA[A/T]CAAAAATGTGGTACT | 84669 |
rs546695393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227294 | TTTTTTTTTGAGACG[C/G]AGTCTTACTCTGTCA | 84669 |
rs546696642 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60254050 | TGCAGACAAGTTATT[A/C]TTTGTTTAAAATGGT | 84669 |
rs546734560 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60241191 | TTTAGTACAGACGGG[A/G]TTCCATCATGTTGGC | 84669 |
rs546750461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60189978 | TCTCCATCAAAATGC[A/G]TGTTGAAATCTGATT | 84669 |
rs546757695 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60233778 | TTCCCTGTCTCTTTA[A/T]TTAGTAAAAACACTT | 84669 |
rs546762414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60347602 | TCGTGATCCACCCGC[C/T]TCAGCCTCCCAAAGT | 84669 |
rs546766849 | in-del | -/T | 0.367503 | 0.220665 | intron-variant | USP32 | GRCh38.p7 | 17:60241446 | TTATTTTTTTTATAA[-/T]TTTTTTAAATCAACA | 84669 |
rs546785543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218978 | CGTCAATAAAGTTTA[A/G]CCTTACAGAGAAATG | 84669 |
rs546798961 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60304362 | CCCTTTATTTTTTTA[-/T]TTTTTTTTTTTTACG | 84669 |
rs546813718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197290 | TAAAACAGAACTCTC[A/G]TTTGTACCATGATGG | 84669 |
rs546820746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288082 | TCACACCACTGTACT[C/T]GAGGCTGGGCAACAG | 84669 |
rs546823032 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | USP32 | GRCh38.p7 | 17:60283906 | ATGTACATCATCCGA[G/T]AACAAACTAGAGCGA | 84669 |
rs546831314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60386953 | TTAAAAACTGCCCCA[C/T]TTTTCTCCTTTACAA | 84669 |
rs546837728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355511 | AATCCAACTTTTTCA[A/G]AACTCTAGAAATCAA | 84669 |
rs546845116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225705 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 84669 |
rs546861627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60270678 | AAAACACAAAATTAG[A/C]CGGGCATGGTGGCAC | 84669 |
rs546870406 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60310485 | GTGGGCAGATCATGA[A/G]GCGAAGAGATTAAGA | 84669 |
rs546894997 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60286260 | GTCTCCCAAACATTC[A/C]TGATTATCTGGAACC | 84669 |
rs546935498 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60239782 | CTGTCACCCAGGCTG[C/G]AGTGCAAGTGGCACA | 84669 |
rs546936112 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60401726 | CTCTATAAAAAAAAG[-/A]AAAAAAAAAAAAAGA | 84669 |
rs546951308 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60291282 | TCAAATCTGATTTTT[-/TA]TGTTTCTGAGTCATG | 84669 |
rs546956521 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265560 | AAGTATATTAAGCAA[A/G]ATTTGTTTTGCTTTT | 84669 |
rs546965037 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60371647 | TCAACATCACTTAGT[C/G]AAGGAAATGCAGATT | 84669 |
rs546978288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60253836 | AAGCAATTCTGTTGT[G/T]TTTATAGTGGTGATC | 84669 |
rs546994070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402302 | GTTGCCCAGGCTGGA[A/G]TGCAGTGGTGCAATC | 84669 |
rs547009053 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | USP32 | GRCh38.p7 | 17:60376218 | GCCCAACTATAATCC[A/G]ATTTTTTATTTGTAT | 84669 |
rs547017408 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60273149 | GGCTAATTTTTGTAT[C/T]TTTAGTAGAGATGGA | 84669 |
rs547041847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271239 | ACTCCATTAAACCTG[C/T]AAACATATGAGAAGA | 84669 |
rs547046776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212225 | AGTTAATTTTAGTAC[A/G]TACATTGCTTAACGA | 84669 |
rs547048225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375547 | ATGAAGTGTACAAAC[A/C]ATACATACTAAATTA | 84669 |
rs547064325 | snp | C/G | 0.000188283 | 0.00970082 | intron-variant | USP32 | GRCh38.p7 | 17:60219601 | TTTAAGGAAATGCAT[C/G]GTATTCTTGCTGCAT | 84669 |
rs547071829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60367076 | TTGTGATCCGCCCCC[C/G]TTGGCCTCCCAAAGT | 84669 |
rs547109861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320865 | GGTTCCAGGAACTAG[A/G]ACCTGGAGATCTTTG | 84669 |
rs547141565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60267762 | CTGACCTTGTGATCC[A/G]CCTGCCTTGGCCTCC | 84669 |
rs547145979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337669 | ACTGCTTGAGCCTAA[A/G]AGTTTGTGACCAGCC | 84669 |
rs547148545 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60329171 | AGGAAACTGTTTATT[C/T]GTAAAAAGAAAGTGT | 84669 |
rs547168374 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60355246 | CAACTCATCAATGAT[G/T]ACAGGTCAGAACAGT | 84669 |
rs547176383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222902 | GGCCAGGCTGGTCTC[A/T]AACTCCTAACCTCAG | 84669 |
rs547184746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60345348 | CATCTAAAACAAAAC[A/G]TTGTTTACCCACTCA | 84669 |
rs547201820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60180481 | GTCCATTATTTCAAC[A/T]AATGTTCCCCAGTTC | 84669 |
rs547204778 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60315727 | GAAGTATTATTTAGC[C/T]ATAAAAAAGAATGGG | 84669 |
rs547213164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60394901 | GGCGCACACCATCCC[A/G]CCCGGCTAATTTTTG | 84669 |
rs547213460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326225 | TGATACATAGATTCA[C/T]CATAAATCAAAGATT | 84669 |
rs547222932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60383075 | ACATGCTGAAACCCC[A/G]TCTATATTAAAAATA | 84669 |
rs547244386 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60333734 | AGAGGAGAGGGAAGT[A/T]AAAGGAAAGGAAAGA | 84669 |
rs547256191 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60370123 | CCATCTCAGCTCACT[A/G]CATCCTCCACCTCCT | 84669 |
rs547259031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288007 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 84669 |
rs547268466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60229780 | TCACTTCTATATTCC[A/G]TTTATATAAAGTTGA | 84669 |
rs547275128 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60387058 | GGTGAATTTTAAAAA[G/T]TCATAGGAAGGCAAA | 84669 |
rs547294420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60195691 | CTAAATGTCGGAATG[C/T]GTATGAACTCAGTTC | 84669 |
rs547327723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236311 | GCACAAAAATTATCA[C/T]TAGAAGTTTTATAAG | 84669 |
rs547338636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60184176 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGCGCCT | 84669 |
rs547341714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60187110 | TCCTGAAACTCATGA[A/T]GGGAACATTAGGCTG | 84669 |
rs547347045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400033 | GCAGTAGTGTGATCT[C/T]GGCTCACTGCAACCT | 84669 |
rs547373209 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60268398 | ACATAACAAGACACT[A/C]TCTCTATTTAAAAAA | 84669 |
rs547378495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317857 | GTGCATGGTGGCATG[A/C]GCCTATAGTCCCAGC | 84669 |
rs547382575 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312728 | GGCAAAAAATATATA[C/T]CTTTCCAAAGAACTT | 84669 |
rs547389559 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60366791 | AAGAAACAGAGACAC[A/G]CTATTACTAAAGTAT | 84669 |
rs547395791 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60217233 | AAATCTAGGATCAGC[A/C]CAAGAGTTACAAAGA | 84669 |
rs547425906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60199628 | TTCTAAGTAAAAAGA[A/C]CCTTTATTCAGATTA | 84669 |
rs547438292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60207303 | CTTGATAAAAATAAC[A/G]GAAAACTAACCTCAA | 84669 |
rs547442610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60357634 | AAAAATGTCCTAAGG[A/G]TACCTTTATCTTTCC | 84669 |
rs547447396 | snp | A/G | 1.76771e-05 | 0.00297291 | intron-variant | USP32 | GRCh38.p7 | 17:60208878 | ATCCAAAAGAGAAGC[A/G]TTTCTATATAAATTC | 84669 |
rs547453059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192175 | GTGCACCTGTAGTCC[A/C]GGCTACTCGGGAGGC | 84669 |
rs547453209 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60341370 | TAAGGCAGGCCTGGT[A/G]GTGACAAAATCTCTC | 84669 |
rs547468917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326603 | TGTGCCCGGCCATGG[C/T]TTATTTTCTCATTCT | 84669 |
rs547499191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60206880 | CGTCGAAAAAATATG[A/G]AATAATCAGTAAGGT | 84669 |
rs547514437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316881 | AATGAAGTTCTGATA[C/T]ACGCTACAAATGGAT | 84669 |
rs547529588 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60365809 | TGCCCAGAACAAATA[C/T]ATAAGAGAAAAACCA | 84669 |
rs547543602 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60363900 | AAAGAAGGAAGTGTT[C/G]GGGGGGCACCTTACA | 84669 |
rs547546211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267361 | GTGATCCAAGATCGT[A/G]CCCCTGCACTCCAGC | 84669 |
rs547556482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60307983 | ACTGACCAGCAGAAC[A/G]ATGCGGAGTTAGGGT | 84669 |
rs547570253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60185228 | ACTGAATTGCAGTTA[C/T]TGGTCTACATGATTG | 84669 |
rs547571615 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60224107 | TGATCTTTACAATAC[A/G]AAAATATGCACAGAA | 84669 |
rs547580460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333224 | AGCCTTACCAAAAAC[A/G]TAAACAGTTGATAAC | 84669 |
rs547587872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412895 | AATCATTAGGCCCCA[A/G]CAATTTTGACAAGAT | 84669 |
rs547597782 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421347 | GGGTGCTCCTCCAAA[C/G]CTCCGGGCCTCCGGG | 84669 |
rs547611509 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60275336 | GTGGCGTGTGCCTGT[A/C]ATCCCAGCTACTCAG | 84669 |
rs547626781 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60304689 | TTGTATAGTACACAT[-/A]AATGTTGTCTATACA | 84669 |
rs547654335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60284463 | CTAACCTTGTGATCC[A/G]CCCGCCTTGGCCTCC | 84669 |
rs547664956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60283914 | CATCCGAGAACAAAC[C/T]AGAGCGAAGGGCTGA | 84669 |
rs547679171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60324235 | TGCAATCAGCTATGA[C/T]TGCACCACTGCACTC | 84669 |
rs547680157 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60399234 | CAAAGTAAAAGCTCC[C/T]GCTCTCATGGAATTT | 84669 |
rs547699575 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60370542 | GAGGCGGGAGGATCA[C/G]TTGAGGTCAGAAGTT | 84669 |
rs547712008 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60366222 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGA | 84669 |
rs547741453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60372985 | GCCTGGCTAACATAG[C/T]GAGGTCTCTACAAAA | 84669 |
rs547747060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183632 | CTCTACATAGGCCCC[A/G]GTGCACTGGTGTGCT | 84669 |
rs547765841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221751 | CCTCGTGATCTGCCT[A/G]CCTCGGCCTTCCAAA | 84669 |
rs547780492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60389995 | GCACTCCAGCCTGGG[A/C]AACAGAGCAAGACTC | 84669 |
rs547782959 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60200968 | GGGCTTGAGAGATTC[C/T]CTTGCCTCAGCCTCC | 84669 |
rs547794442 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60287815 | AAACAAAACACTGAC[-/A]AAAAAAAAATTTCTC | 84669 |
rs547807150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332230 | GCCACTCCAGCCTGG[A/G]TGACAGAGCGAGATG | 84669 |
rs547808575 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60384000 | TGGCAGTGGGGACTA[A/C]AGTGGAGGCAATTAA | 84669 |
rs547827948 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60338886 | ATAAGCAAGATTAGA[A/C]GTACATAAAAATATT | 84669 |
rs547844672 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60281602 | ATAATAACAAAAGGT[-/A]TTACCTAATTTACTC | 84669 |
rs547850938 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60273489 | TTACAAACAATCCTG[G/T]AAAATATGGTGCTGA | 84669 |
rs547861776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298937 | AGTCCAGCCTGGGCA[A/G]CCTAGCAAGACCCTA | 84669 |
rs547881423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390895 | TACAAGCATACACAG[A/G]TCTACACACACTGAA | 84669 |
rs547931532 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420290 | TGAGCCACCGCACCC[A/G]GCAGAATTATGTTGT | 84669 |
rs547938642 | snp | C/T | 0.000399281 | 0.0141238 | missense | USP32 | GRCh38.p7 | 17:60236239 | CTCGTTCTAACCATC[C/T]TCTGTATGTACAAAA | 84669 |
rs547945882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60260068 | GTTAAAGGCATCTGG[A/G]ACTGTAATACATTAT | 84669 |
rs547962201 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60199933 | AGGTGCAGTGGCTCA[-/T]GCCTGTAATCCCAGC | 84669 |
rs547965219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60365270 | TGGATCATGAGGTTA[A/G]GAGTTAGAGACCAGC | 84669 |
rs548000943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373594 | AGCTAGGATTACAGG[C/T]GTGCACCACCACAAC | 84669 |
rs548007976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60259385 | ATGCTGTGATGTAAA[A/G]AAACAAAAAAATGAA | 84669 |
rs548020350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60266519 | TTGGAGATGGAGTCT[C/T]GCTCTGTCGCCCAGG | 84669 |
rs548046753 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60270471 | AACCCAAGTATTCAT[A/G]TTCAAAATATGATTT | 84669 |
rs548046792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60340872 | CAGGCCTGGTGGTGA[A/C]AAAATCTCTCACCAT | 84669 |
rs548056121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60398418 | AAAAAAGAAAAAAAA[A/G]GGTGTTTTGGCAACC | 84669 |
rs548067847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60283811 | AGAAATACCTCAAGA[A/G]CAGAAAAGTTCATCT | 84669 |
rs548075356 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60221318 | ATATTGTTCAAACCC[G/T]GGAGCTTGAGGTTAT | 84669 |
rs548082541 | snp | A/T | 1.64912e-05 | 0.00287147 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266078 | ACGGTCAACATCAAA[A/T]ACCTTGAAGCAAACT | 84669 |
rs548084169 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60203557 | TTTACTTGATCTAGA[A/G]GCCTTGCTTTCCTTT | 84669 |
rs548114727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228942 | AAAGTGGTGGGATTA[C/T]AGGTGTGAGCCACCT | 84669 |
rs548114810 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60381269 | CAACAGTGAGATTCC[C/T]GTCACTACAACAAAA | 84669 |
rs548122299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243239 | TGCTGAACTCATTTT[A/G]TTAATTCTAACAGTT | 84669 |
rs548123737 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60316263 | CTCAAAAAAAAAAAA[A/C]AATTCTCTCTTCCCT | 84669 |
rs548152744 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60387455 | CTAGGCCATCAGAGA[C/T]ACCCATACACACTCT | 84669 |
rs548162928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326092 | AGCTAGGTAAGGATA[A/G]GAACTCTTGTTTTCA | 84669 |
rs548163449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60260506 | CCAGCCTGGGTGACA[A/G]GAGCAAGACTTTAAA | 84669 |
rs548163980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60357448 | ACAGAGCAAGACCCT[A/G]TCTCTTAAAAATAAA | 84669 |
rs548168505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405696 | GAGCCTGGGGAGGTG[A/G]AGGCTGCAGTGAATC | 84669 |
rs548198969 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60366000 | GTTGTTTTTTGAGAC[C/G]GAGTTTCGCTCTTGT | 84669 |
rs548202688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60365220 | GTGCGGTGGCTCATA[C/T]CTGTAATCCCAGTAC | 84669 |
rs548202761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356681 | AAATAGCAGTAACAA[A/C]CCTTAAGGTAGGGAA | 84669 |
rs548208601 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60201445 | AACTAGAAAATTGTA[C/T]TCCAAAGTAGTTGTT | 84669 |
rs548211872 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60198927 | GAGATCAGAATGGGC[A/T]ATGTAGGGAGACCCT | 84669 |
rs548238834 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60345942 | AGCCAAGACCATGCC[A/G]CCGCACTCCAGCATG | 84669 |
rs548238966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60364461 | GTCCACTCACCGCAA[A/C]CTTTGCCTCCCAAGT | 84669 |
rs548263581 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60394563 | TAATAGAATATGACC[G/T]CATGTGTCGTTTTCC | 84669 |
rs548288743 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60256175 | GACACCATCTCTTTG[-/A]AAAAAAAAAATAATA | 84669 |
rs548297985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325240 | CCAACATGGTGAAAC[C/G]CTGTCTCTACAAAAA | 84669 |
rs548313182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259328 | TATTCATATATAGCA[C/T]ATATGCCCTTTTTGT | 84669 |
rs548328717 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60281089 | ACTGTCTTTCCACAA[A/G]TCTGGGCAAGTTAAT | 84669 |
rs548330659 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60206476 | TTCTATTGGACAGTG[A/G]TGCTCTAAACTAAAA | 84669 |
rs548333191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60229114 | AGGGTCTTGCTCAGT[C/T]GCCTATAGCTCACTA | 84669 |
rs548344613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373497 | CACCCAGGCTAGAGT[A/G]CAGTGGCACGATCTT | 84669 |
rs548345764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60213035 | TGGGATTACAGGCGT[C/G]AGCCACTGCGCCCGG | 84669 |
rs548354782 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60236482 | AAAAACTTAAAAATT[-/A]AAAAAAATTAGAAAA | 84669 |
rs548362037 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60302439 | GGCATGAGCCACCGC[A/G]CCTGGCCTGAGCACA | 84669 |
rs548367405 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60275529 | CACATACCCCCACAC[C/T]CCTCTTCAGGATAAT | 84669 |
rs548373983 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60254988 | CCACTTTCCTATTTC[C/T]CACGTCACGATTTTG | 84669 |
rs548376987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332294 | CGGTTTTGTCATGCA[C/T]ATATACCAATCACTA | 84669 |
rs548382012 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411273 | AGGTTGCGGTGAGCC[A/G]AGATTGCCCGATTGC | 84669 |
rs548389352 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60184148 | AAATAAATAAATAAA[A/T]AAAAAACACACAAAA | 84669 |
rs548452507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183516 | TACAAAATTTACATG[C/G]AAAAAACAAGTCAAA | 84669 |
rs548465005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60191549 | GAGCCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 84669 |
rs548465918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60331334 | ACTTTGGGAGGCCAA[G/T]GCAGGCGGACTGCTT | 84669 |
rs548477425 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405075 | GAGGCTGAAGCACAA[C/G]AATTGCCTGAACCAG | 84669 |
rs548511668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348250 | AAGAGAGGTTGATAG[A/G]AGTCATCAGTATAGA | 84669 |
rs548524372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298865 | TGCTAGCTCATGTTT[A/G]TAATCCTAGCACTTT | 84669 |
rs548526062 | snp | C/T | 9.88712e-05 | 0.00703035 | missense | USP32 | GRCh38.p7 | 17:60190585 | TGGGATGTTTGATAG[C/T]GAAGGTGAAGGGCTG | 84669 |
rs548544075 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60358412 | AAACCCCATCTCTAC[C/G]AAAAATACAAAAATT | 84669 |
rs548573122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281827 | CAAAATCACCCTGGA[A/G]GTCTGTAAAGTACAA | 84669 |
rs548579513 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60205851 | TAACTCACACTTTTG[A/G]CCAAATGAAAAGGAA | 84669 |
rs548585425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228112 | CTCACAGCAACCTCC[A/G]CCTCTAGCTTCAAAT | 84669 |
rs548600652 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60312578 | CCCAAGTAGCTGAGC[A/G]CACAGGAACATGCCA | 84669 |
rs548600854 | snp | C/T | 1.66835e-05 | 0.00288816 | intron-variant | USP32 | GRCh38.p7 | 17:60198248 | AGGTTTAGATGGATC[C/T]CCTGAACTCACCAAT | 84669 |
rs548604246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60202937 | GAAAGACAGAGAGAA[A/G]GAGAAGGCTATATGA | 84669 |
rs548645488 | snp | C/T | | | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413989 | GGGAACAGTCCTCTG[C/T]TCCCCCTTATCTGAG | 84669 |
rs548646784 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60372607 | CACTTTGGAAGACTG[A/C]GGTGGGAGAATCACT | 84669 |
rs548661603 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60205794 | ACAGTATAAATAATT[A/C]TAGATTTATTGGAAG | 84669 |
rs548669701 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60230619 | CAAACAAACTAGACT[C/G]GTCTGTCTTCTCATT | 84669 |
rs548681088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306497 | ACAAAAATTAGCTGG[G/T]CGTTGTGGTGGGCGC | 84669 |
rs548683814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60210599 | GGCGTGAGCCCCTGC[A/G]CCCAGCCTACTTCTT | 84669 |
rs548710250 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60348200 | GGAAACCTTGGAAAA[C/T]GCAATGGGGTTTTAG | 84669 |
rs548718334 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60302197 | CTGGAGTGCAATGGC[A/G]TCATCTTGGCTCACT | 84669 |
rs548723962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60246957 | TGAATGGATAGTTTG[C/T]AAATATTTTCTCCTA | 84669 |
rs548726516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318643 | CCAAACCCAGAAAAC[A/G]AGGCTGGGACTAGGT | 84669 |
rs548727312 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419295 | GCATGTTCTCACTTA[C/T]AAGTAGGAGCTAAAT | 84669 |
rs548736987 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60328897 | GTCTTGACTGCACAC[C/T]GGCTGTACCCCACTC | 84669 |
rs548743858 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194303 | CCTGCCTCAGCCTCC[C/T]AAAGTGCTGGGATTA | 84669 |
rs548745798 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417117 | GAGACTGGTTTTAAC[C/T]GTGTTGGCCAGGCTG | 84669 |
rs548754610 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393095 | TCTTGCAAAAGGGAA[A/C]CTCTGTGCCTATTAA | 84669 |
rs548789501 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60381110 | CCTTTAAGGAGAAAG[C/T]ACAGCAGCACTAGGT | 84669 |
rs548790276 | in-del | -/TTAAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60395615 | TCAATTTCATTATAA[-/TTAAC]TTAATCCATTGAAGA | 84669 |
rs548796981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265822 | AAGCCAAACTCTCTT[C/T]CCAATTTTGCATCTT | 84669 |
rs548824706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60310661 | CCAAGATCGACCCAC[G/T]GCACTCCAGCCTGGG | 84669 |
rs548841031 | snp | A/C/T | 1.86027e-05 | 0.00304976 | intron-variant | USP32 | GRCh38.p7 | 17:60255310 | TTTCTTTTTTTTTTT[A/C/T]TTTTTGAGACGGAGT | 84669 |
rs548861925 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60317982 | AGAGCCAGACTCCGT[C/T]TCAAGAAAACAGAAA | 84669 |
rs548874510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60272464 | AATTTACAAAGCGTA[C/T]ATAGGACATTTATTC | 84669 |
rs548896266 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60368265 | ACAACAGCACTGGAT[A/T]GTATAATGCTTCCTG | 84669 |
rs548899178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326834 | AGTTATATTTATATA[C/G]ATTACTATCCTGCCA | 84669 |
rs548900966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60396999 | AAGCTCCTGAAAAAA[C/T]CAAGTAGCATCCTTT | 84669 |
rs548924996 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60359818 | CTTGTCTCTGAAAAT[A/G]ATAGATAAATAAAGA | 84669 |
rs548930141 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177738 | TTTCAATTTAGGTAG[C/T]CATTTAAGATAACCT | 84669 |
rs548951865 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409000 | ACCCAGACCCCAGCT[C/T]GGGGAGACACAGCTG | 84669 |
rs549016114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60368904 | AAATGAAAAAGTTTC[C/T]GATGCAAGACAACAT | 84669 |
rs549037700 | in-del | -/TCAA | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60297393 | GAATAAAACCCTGTC[-/TCAA]TCAATCAATCAATCA | 84669 |
rs549088788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416453 | TAACAACCCACAACC[C/T]CCTCACCTGCCAGAT | 84669 |
rs549118140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414676 | TCAGGAGATCCACCC[A/G]CCTTGGCCTCCAGAA | 84669 |
rs549118458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60342804 | ATTTGGGCAGGAGTG[C/T]CCCGTTTTTCTAGTT | 84669 |
rs549188684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218122 | AATTACTACGAAACA[C/T]TACTGAAAGAATTCT | 84669 |
rs549205508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60269305 | TTAGAGTGACCTCAG[C/T]AAAACCCTAACATGA | 84669 |
rs549227271 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60376708 | TTTGTATTTTTAGTA[C/G]ACAGGGTTTCACCAT | 84669 |
rs549228655 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60196123 | AATACAAAAATTAGC[C/T]GAGTGTGGTGGCATG | 84669 |
rs549234966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192705 | GATGGGAATACAGGC[A/G]TGAGCCACCGTGCCC | 84669 |
rs549251300 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60239235 | ATTGTATGGGACAAA[C/T]AGCTTCTCTTTTGCT | 84669 |
rs549253109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413842 | TGCACTCCAGCCTGG[A/C]GACAGCTAGATTCTG | 84669 |
rs549265725 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412527 | GTGACAGAGTGATAC[A/C]CTGTTTCAAAAAAAA | 84669 |
rs549268710 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60268616 | AAAAAGATTTTAGCT[G/T]CCTCATCTAAGAGCA | 84669 |
rs549291857 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, synonymous-codon | C17orf64, USP32 | GRCh38.p7 | 17:60422256 | CTTACCAGGTGGTGT[C/T]AGGATCAGCATCTGA | 84669 |
rs549294559 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60335219 | GCTCAAGCAATCCTT[C/G]AGATTCCGAAAAGTG | 84669 |
rs549297944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261185 | AATGATTCTGCACTG[A/T]TGACAAAATTAACAG | 84669 |
rs549333088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60253676 | GAGGTTGAGGCAGGA[A/G]AATCGCTTGAACCTG | 84669 |
rs549342965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360702 | AAACAAAAACTAAAA[C/T]TATACAAAATACATG | 84669 |
rs549359116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60245819 | TTTTCAGTGTTCATA[C/T]AGGAATGTCTTTAGT | 84669 |
rs549366841 | snp | C/T | 0.000355038 | 0.0133189 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231568 | TGGCAGTCCTGACGA[C/T]GATCCTCGAGGGCTG | 84669 |
rs549379107 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60360240 | AGCACTTTGGGATGC[A/G]AGGTGGCCTTCTGAC | 84669 |
rs549379850 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405202 | AAGCTGTTAGTTTTT[C/T]GTTTTTGTTTTTGTT | 84669 |
rs549389248 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60368222 | AGAGAAATACAGTAT[G/T]TAGAGATACTGAAGC | 84669 |
rs549392443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60309142 | ATAGACAAATGGGAT[C/T]TGATCAAGCTAAAAA | 84669 |
rs549398739 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409803 | TCTTGGACCACACAT[A/G]AAATACACTAACACT | 84669 |
rs549417453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60193955 | ATAGAAAGCTGTGCA[A/G]CACTTCCCTTCTGAA | 84669 |
rs549422796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60371736 | ATATGAAGCACCAGT[C/T]CTGCAAGCTCCTTTC | 84669 |
rs549426070 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328994 | AGGCTGGTAGTGTGA[A/G]CCTGCCAGGCCAAGT | 84669 |
rs549427310 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60316733 | GTAGTCCCAGCTACT[C/T]GGGTGGCTGAGGCAG | 84669 |
rs549437650 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60192591 | AGGCACGCATCACCA[C/T]GCCCCGCTAATTTTT | 84669 |
rs549441537 | snp | A/C | 0.000165824 | 0.00910409 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392663 | GCAGGGAGCTCCCAA[A/C]CTTAGGGACGTCTTT | 84669 |
rs549469640 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60383247 | TCCCAAAAAAAAAAA[A/C]AAAAAACTTTAAGCA | 84669 |
rs549477065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60217275 | AAGTGCAACAACACA[C/T]CTTGCCTCTCATGTT | 84669 |
rs549478435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237927 | ACCTGTTTTCAATTA[C/T]TCTGGTATATATTTA | 84669 |
rs549501139 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60245487 | GGGCAGCATGTGGTT[A/T]GTTTTTTGTTGCTGA | 84669 |
rs549540356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216434 | AACTTATCAATATAA[C/T]GTACATTCCAAATAA | 84669 |
rs549542559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60364064 | GGGAAATTTACTGCT[C/T]ACAGCTCTGGAACCT | 84669 |
rs549543199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201350 | CTACTATAGATAATG[C/G]TGCTACGAATATTCT | 84669 |
rs549543445 | in-del | -/AGAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60401379 | GTCTCAATTAAAAAG[-/AGAA]AGAAAGAAAGAAAGA | 84669 |
rs549549064 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60301423 | GTATCTCACTGTAAT[A/T]TTAATTTATATTTCT | 84669 |
rs549584696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360096 | GATGGTCTTGATCTC[C/T]TGACCTCGTGATCCA | 84669 |
rs549606387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60209857 | TAAAACAGCGTTTGC[C/T]CACATTGAAAGACAT | 84669 |
rs549621343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60359245 | AATATCAAATTCTCA[A/G]TGCTTTAACTTTAAA | 84669 |
rs549623091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317967 | TCCAGCCTCGGCGAC[A/C]GAGCCAGACTCCGTC | 84669 |
rs549650307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60199993 | GAGGTCAGGAGTTCG[A/G]GACCAGCCTGGCCAA | 84669 |
rs549657207 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60334524 | AGTGAAACCTCGTCT[C/G]TACTAAAAATACAAA | 84669 |
rs549661921 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60380004 | TGTGTTATTTATGTA[C/T]ATATATATGTAAAAA | 84669 |
rs549668226 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60297454 | TTCCTTTTCTTTTTT[C/T]TTTTTTCTTTTTGAG | 84669 |
rs549668284 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60261894 | TAATACTGTCCAAAA[A/G]GAAAGAAACGTCATG | 84669 |
rs549669065 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60308189 | AAGAATCCGGGATAC[A/G]GAAAACCCTTGCGAT | 84669 |
rs549694284 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60400696 | CTGGAGACATAGGTT[A/G]AGGAGTCATTAGAGA | 84669 |
rs549695765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333795 | GTACTGTACTGTTTT[A/T]ATCATAAGTTTATGT | 84669 |
rs549697017 | snp | A/C/G | 1.76191e-05 | 0.00296804 | synonymous-codon | USP32 | GRCh38.p7 | 17:60208760 | CTTGCATTTTACTTG[A/C/G]GATCTTAGCTGCCCA | 84669 |
rs549707176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216110 | TATTAGCCTGTCCAC[C/G]CAGTAAGTTGACGAC | 84669 |
rs549710515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60376480 | AATCAAACAAAGCCA[C/T]GCAGTGAAATGACAT | 84669 |
rs549744205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384685 | TAATCCCAGCTACTC[C/G]GAGGGCTGAGGCAGG | 84669 |
rs549748685 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60298106 | CACCCCAAAGTAAAC[A/G]TCGGGCCTAACTGTA | 84669 |
rs549754870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60262527 | GTCCTCCGTTTAAAT[G/T]TGGCCCTGATTTTCA | 84669 |
rs549769235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60350200 | TGAATTTTTAAATAG[C/T]GATGGGGTTTTGCCA | 84669 |
rs549781267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60210472 | ATGCACCACTATGCC[C/T]GGCTAATTTTTTTTA | 84669 |
rs549807885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377355 | ATTTCATTTTTAAAA[A/G]TGCCTACAAAAGCAG | 84669 |
rs549821102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60192287 | CAGAGCGAGACTCCA[C/T]CTCAAAACAAAACAA | 84669 |
rs549838575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414920 | CAGTGGTGCAATCTC[A/G]GCTAGCTGCAACCTA | 84669 |
rs549840878 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60310612 | GCTGAGGCAGGAGAA[G/T]CACTTGAACCCGGGA | 84669 |
rs549841199 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60302051 | TGATTTGCACTAGAT[G/T]ATTTTGCCCAACTGA | 84669 |
rs549866757 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60237323 | TTTTTTTTTTTTTTT[C/T]TTAACTAGAGACAAG | 84669 |
rs549882645 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60199922 | AAGCCAGGGCCAGGT[A/G]CAGTGGCTCATGCCT | 84669 |
rs549886703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308897 | CTGTGCCACTGCACT[C/T]TAGCCTGGTGACAGA | 84669 |
rs549886995 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60374184 | TGAGACTCTGTCTCC[-/A]AAAAAAAAAAGAAAA | 84669 |
rs549887265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185317 | CATCTCTGTATTCAA[A/C]ATAAAAAGCTTGTAC | 84669 |
rs549911690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60350360 | GTGGCATGATCTTGG[C/T]TCACTGCAACCTCCA | 84669 |
rs549919193 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422135 | AGACCTCTGTCCCAA[A/T]TCAGAAAAGAATTTT | 84669 |
rs549990187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267855 | TCTTGCTGTCTCCCA[C/G]GCTGGAGTGCAATGG | 84669 |
rs549999213 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60308070 | CTTCCCAATCCCCTT[C/G]TGGCTCACCGTCCAG | 84669 |
rs550012157 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60314534 | TCCAATCTGAAGTAC[G/T]GTGAAGAAAAAGAGC | 84669 |
rs550026200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413734 | GCTGGGCATGGCAGC[A/G]TGTGCCTGTAATCCC | 84669 |
rs550037348 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60316225 | CATGCTTAAGAATAT[A/G]CTATGATGAGTAACA | 84669 |
rs550037680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326263 | ATCACACCCTCTGCC[C/T]TAGTAACCTGATTTC | 84669 |
rs550048349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358978 | GAACCAGAAGGTAGA[G/T]ACACACGAGAGGTTC | 84669 |
rs550053121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60276167 | GAGGATTGCTTAAGT[C/T]TAGGGGTTTAGGACC | 84669 |
rs550067328 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60277994 | TCAATGTGGCCTCAA[-/C]CTCCTGGGCTCAAGT | 84669 |
rs550073520 | snp | A/T | 0.000497141 | 0.0157583 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392596 | GCAGAATCTTAGGGA[A/T]TGGGGTTCTGAGGGA | 84669 |
rs550074276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315616 | AGATTCAAACAGATA[A/C]TTGTATGCCAATATT | 84669 |
rs550107756 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60400536 | ACTCACTGAGATGAG[A/G]AATACAACAGGAGAA | 84669 |
rs550109618 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60392008 | CTCCCGCCTTCTCCT[C/T]GGCGTCCCTGGGTGA | 84669 |
rs550113964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60284516 | TGAGCCACCACGCCC[A/G]GCCTAATTCAAGATT | 84669 |
rs550125330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60338345 | AAAAAAAAAAAATAC[C/T]ACATAGAAATGTTTT | 84669 |
rs550141092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60207590 | ACATGATTGGTGTCA[A/G]TTTGTCTTTACTCTT | 84669 |
rs550143713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60181785 | AGATTCACAAATTCA[A/T]ATGCCACAAAGTAAG | 84669 |
rs550148573 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60319135 | GCCGAGTTTCTGTTT[C/G]GGATGATGAAAAGGT | 84669 |
rs550170662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236563 | CATGTAACCAATGAT[G/T]TTCTTCAAAACAGCC | 84669 |
rs550175682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60267173 | AGTACTTTGGGAGGC[C/T]GAGGTGGGCGAATCG | 84669 |
rs550193161 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60184477 | AAGAAAAACCTACAT[A/T]CAGCTTCACAGAGTA | 84669 |
rs550204344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60215209 | ACTCCTGGGCTCAAG[C/T]GATCCACCTGCCTCG | 84669 |
rs550207075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60189866 | AACAGAGAGATGCTT[A/T]TTGATATGTCATGGC | 84669 |
rs550214034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244731 | CTGCCTCCTGGGTTC[A/G]AGTGATTCTCCCACC | 84669 |
rs550247027 | in-del | -/AAT | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60349132 | ATGACTAAATATTAG[-/AAT]AACATAGTATTAGAA | 84669 |
rs550282730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60296909 | CCTTAAAAACAGATA[C/T]TGGTCATGAGGGGAT | 84669 |
rs550304555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412965 | CTCTAAAGTTCCGAG[G/T]TTGCCATTCTGCAGT | 84669 |
rs550324512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60234030 | TCATGGCTCACTGCA[A/G]TCTTGACCTATCAGG | 84669 |
rs550326223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243852 | CATATATCATCATTT[A/G]TCATAATAAAATGTC | 84669 |
rs550336377 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60372332 | ATCGTTAGGTGATTT[C/T]ATCATTGTGCAGACA | 84669 |
rs550353851 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405673 | AGGCTAAGGTGGGAG[A/G]ATCACCTGAGCCTGG | 84669 |
rs550361312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197204 | AAAGATGTATTTATC[C/T]TAAGCCCTACCCTAA | 84669 |
rs550365272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60288152 | AAAAGTCTTGGCTGG[A/G]CACAGTGACTCACAA | 84669 |
rs550381359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60366684 | GGCAGGAGGATCACT[C/T]GAGCCCAAGAGCTTG | 84669 |
rs550401077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60305026 | ACATCAATGAAGCAG[C/T]AGAGTCAGAATTTTA | 84669 |
rs550418810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60259444 | TGAGTGTGGATATAC[A/G]TGTGAGCGCGCCCTT | 84669 |
rs550445547 | snp | C/T | 1.65329e-05 | 0.0028751 | missense | USP32 | GRCh38.p7 | 17:60207048 | GACTAGAAGCTGAAA[C/T]TGGAGACACAGGGAC | 84669 |
rs550457071 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60374388 | GCCTAAGGCTGTTAC[A/G]GTTAAGTTTTGTTTT | 84669 |
rs550459855 | snp | G/T | 0.000399281 | 0.0141238 | missense | USP32 | GRCh38.p7 | 17:60214750 | AATACCCGCTTTAAA[G/T]GTGCATTCGGAGAAG | 84669 |
rs550507468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234428 | CAAGCATGACTAATT[A/T]AAAAAAAAATTTTTT | 84669 |
rs550510465 | snp | A/G | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422923 | GGTTGTGTGGTGTGT[A/G]TGCTGTGTTGGAGGA | 84669 |
rs550537954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281223 | GTGTTCACAAATATA[A/G]GAGGATGCATATTCA | 84669 |
rs550571217 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60270556 | AGACTGGGCGCAGTG[A/G]CTCACGCCTGTAATC | 84669 |
rs550578500 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60387631 | TCTAGTATTTTATTC[A/G]CATCCTCTATGAATA | 84669 |
rs550601824 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60228279 | CCTTGGCCTCCCAGT[A/G]TGCTGGGATTACAGG | 84669 |
rs550616963 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60311889 | GAAACAGTTGTAGCA[A/T]GTTTCAACTGCTGCT | 84669 |
rs550618014 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60355576 | CAGAAAAATGACTGA[C/G]CTGAGTGCGGTGGCA | 84669 |
rs550633317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256488 | ATAATGTTTCATTCA[A/G]TATCATTTTATTATA | 84669 |
rs550634278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60395969 | CCAACACATTAAGAG[A/G]ATTGATTTTTCAGTA | 84669 |
rs550634538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60279342 | TTTTTAGAAATTAGC[C/T]GGGTGTGGTGAATGC | 84669 |
rs550645419 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60309549 | CGATGTTGCAGTGGG[A/C/T]CAAGACTGCACTACT | 84669 |
rs550663226 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60223855 | TCATAATGAGAATTA[C/T]ATGTCCTCCGACTGG | 84669 |
rs550668153 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178774 | TTGCACACCTTCGTG[A/G]TCTTGCTTTCTCCAT | 84669 |
rs550668598 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410439 | TTTGGGAGGCTGAGG[C/T]GGGCAGATCACAAGG | 84669 |
rs550670572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196773 | GAGGTTGCGTTGAGC[C/T]GAGATTGCACCACTG | 84669 |
rs550681939 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60290714 | ACCCCACAGCTGGGT[-/G]GGGGGGCTGCTAGAT | 84669 |
rs550688337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355398 | TAAAAATTTTCCCTC[A/C]AAAAAAACCTGTAAG | 84669 |
rs550696005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60263480 | AAAAACCCAAGTTCT[A/G]TCCCAAACTATTACT | 84669 |
rs550708652 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60288978 | TTTGCTAAGTATATC[A/C]CAAAACCAGTAAACT | 84669 |
rs550725833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249395 | CTGGGGACATGAGAA[A/G]GCTTGCTAAGGCTCA | 84669 |
rs550725902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378310 | AGTATTGGGTAGATA[A/T]GGAGAAAATGGAAGG | 84669 |
rs550738548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183837 | TTGTGGCAGTTCTCA[C/T]ATCACACTGAATTGC | 84669 |
rs550741947 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60385098 | CCTGCCTTAACCGAT[C/G]ACATTCCACCATTGT | 84669 |
rs550762765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60386808 | ATATATTTATCTCCT[C/T]TTGTCAGAGACACAC | 84669 |
rs550770743 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363267 | CGCAACCAGCCTAGG[A/C]AACACGATGAAACCC | 84669 |
rs550779574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60238791 | CCTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA | 84669 |
rs550787104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60248683 | TTATTGCTATTTTCT[A/G]TTTGGACAAGTCAGT | 84669 |
rs550794359 | in-del | -/ATTATTATT | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419854 | ATTATTATTATTATT[-/ATTATTATT]TTATTATTATTATTT | 84669 |
rs550807614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362726 | TTCTCGAATCAAATA[C/T]ACAATTTATCATTCT | 84669 |
rs550817827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60264161 | TACATGTTTATTTTT[A/G]CTATTACATGCTTAT | 84669 |
rs550825584 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283330 | TCAAGGATAGGAAAC[G/T]AAGAGACTCTGAAGC | 84669 |
rs550835479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60217056 | AGAAGCATATAAGTA[C/T]AGTATTCAAGTCAAT | 84669 |
rs550835929 | in-del | -/AATT | 0.00258799 | 0.0358789 | intron-variant | USP32 | GRCh38.p7 | 17:60236513 | ACAACTGGTGTTTCC[-/AATT]AATTAATTAATTACA | 84669 |
rs550856092 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60370315 | TACAACTACCAAAAA[C/T]GGGAAAGGTTCTACT | 84669 |
rs550863022 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178752 | TCGTCCATGCCTTAA[A/G]AATCATTTGCACACC | 84669 |
rs550866456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60320786 | GAAAGGGTAATAAGC[A/G]ATAAAACTAGCATTT | 84669 |
rs550894509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212148 | TCTATCTAATTTATA[A/C]CCATTCGATTGCTTT | 84669 |
rs550900845 | snp | A/G | 0.000399281 | 0.0141238 | stop-gained | USP32 | GRCh38.p7 | 17:60211428 | ACTGTGTCAGTGGCT[A/G]TGTGTTACTAACACA | 84669 |
rs550905059 | snp | A/T | 0.000259341 | 0.0113843 | intron-variant | USP32 | GRCh38.p7 | 17:60219594 | TTTTTTTTTTAAGGA[A/T]ATGCATGGTATTCTT | 84669 |
rs550928959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60345670 | AGGTGTCTCATAATT[C/T]TTTTCAACCTGGCTC | 84669 |
rs550952251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60379142 | AAATCATAATTTAGT[A/G]CAATTTTTTGCTTTC | 84669 |
rs550953252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60294360 | GACACTACAACATGA[A/G]CACTGTTTCAGGTTC | 84669 |
rs550964222 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60218912 | TATTTCTTTACTGCT[C/G]AAGAATAATTTCAAA | 84669 |
rs550965787 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60397789 | ATTATCCTGATACTC[-/A]AAAAAAATTCTGAGA | 84669 |
rs550989035 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60387460 | CCATCAGAGACACCC[A/G]TACACACTCTGTATT | 84669 |
rs551018707 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60195978 | AATTGTTCAGGGTAA[A/G]AAGCCGGCCTGGGCC | 84669 |
rs551018739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60203870 | ATGAGCCACTGTGCC[C/T]GGCCTTTCCTTTACT | 84669 |
rs551030623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60352420 | AAGCCTAGATGACCA[C/T]GGAACTGCCATATGA | 84669 |
rs551034293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60179631 | AAAATATTTTGACCA[C/T]AGACAAGTCAAAAAA | 84669 |
rs551045041 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60368766 | TCTATACACAACCTC[A/G]AAATGGCAACATTAT | 84669 |
rs551080016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60203333 | TTGAACCCAGGAGGC[A/G]GAGGCTGCAGTGAGT | 84669 |
rs551084163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60312546 | TCCTCCCAAGAGTCC[C/T]TGGGAGTCTGAGGAC | 84669 |
rs551104901 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60250617 | CAAGAAAACACTCAA[A/G]AATATCAAGACTGAG | 84669 |
rs551112399 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60199403 | GAGATATTTACGATA[-/T]TCCTTAATATAGAGA | 84669 |
rs551121421 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60336579 | AAATTAGCCGGGCGT[A/G]GTGGCGGGCGCCTGT | 84669 |
rs551123101 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60341586 | CTCATATTTCTTGGC[A/G]GCTTTGTTCATTTCT | 84669 |
rs551177387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60187674 | ACAGGCTACAGTGCT[A/G]GATGAAGACAGGAAA | 84669 |
rs551178348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295492 | TAAATGGAAATTTCC[A/G]GAAATGAACAATTCA | 84669 |
rs551186888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60320377 | GTAAGATAAATTACT[A/G]TATCTACCCAATTAT | 84669 |
rs551210759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60303919 | ACAGAAAACCCAAGA[G/T]CTGTGAGATCATATC | 84669 |
rs551231048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353507 | GCACTTTGGGAGGCC[A/G]AAGCAGGTGGATCAC | 84669 |
rs551241314 | in-del | -/AC | 0.0854719 | 0.18823 | intron-variant | USP32 | GRCh38.p7 | 17:60349676 | TACACATATATATAT[-/AC]ACACACATATATATA | 84669 |
rs551256919 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60358413 | AACCCCATCTCTACC[A/T]AAAATACAAAAATTA | 84669 |
rs551278415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60201946 | ATAGGCGTGAGCCAC[C/T]GCACCCAGCCAAGTT | 84669 |
rs551307277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60240293 | CTTTCACTGACTGCT[A/G]TAGTTGTTTGTTTAG | 84669 |
rs551337738 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60359535 | GTTTTTTCAAGCAGG[A/G]CACAGTGGCTCAAAC | 84669 |
rs551362142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354244 | CTTATCTCTCCAAGT[A/G]TATTTTAAGTCTCTT | 84669 |
rs551388341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218166 | GAGGTGGATGGATCA[C/T]GAGGTCAGGAGATAG | 84669 |
rs551405697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60278459 | ATGAAGAGAATCTAA[A/G]GGTTAACTAGGGAAA | 84669 |
rs551414385 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60322109 | TGTTTTATAAGATGT[A/G]TTTAACATAAGACTC | 84669 |
rs551440812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402792 | GCCATTTAGTGTCAG[C/T]TGCAGTGGCCTGAAA | 84669 |
rs551441863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60304829 | GACCTCATTAATAAA[C/T]TCTTATTTTTATAAT | 84669 |
rs551451804 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60396874 | CTGTCTCGCCCTTCT[C/G]TACTCCAACTGCAAT | 84669 |
rs551459968 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60327369 | CCTGTGCTCCACGTC[A/C]CCGAAGCAGCCCATG | 84669 |
rs551471452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60188091 | GTTCAAGCAGCCCTC[C/T]AACCTCAGCCTCCCA | 84669 |
rs551471579 | snp | C/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60401283 | GCTGAGGCAGGAGAA[C/T]AGCGTGAACCAGGGA | 84669 |
rs551483476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402320 | CAGTGGTGCAATCAT[A/G]GCTCATTGCAGCCTC | 84669 |
rs551487634 | in-del | -/GTG | | | intron-variant | USP32 | GRCh38.p7 | 17:60182627 | AATTAGCCAGGTGCA[-/GTG]GTGCATGCCTGTAGT | 84669 |
rs551491220 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60392406 | CCCATCTTCCCGCCA[A/G]TCGCAGCCGCGCGCC | 84669 |
rs551492685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60335416 | CTTCCACAAAGTCCT[A/G]TCCAGTTCCTACATT | 84669 |
rs551516955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60385461 | TGAGGCAAGAGAATC[A/G]CTTGAACCAGGAGAC | 84669 |
rs551520156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409072 | ACTTTTCTCAGCCGG[G/T]CACAGTGGCTCATGC | 84669 |
rs551555281 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393517 | CAACCTAAAAGTCAC[A/G]GAATAAAGCTTCTGG | 84669 |
rs551556320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263401 | AAGAGTTGGAAGTCA[G/T]AAAAAGAATGAGTAA | 84669 |
rs551578695 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211351 | AAGTCACAGGTTAAG[A/T]GGCCAGTGACTCCAG | 84669 |
rs551593096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256220 | CCTCCAAATCAGAAT[A/G]GAGAAATAAGCTAAA | 84669 |
rs551594011 | snp | C/G | | | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231609 | CCAGCCTTGGCTAAG[C/G]AGAACAGGGACCCCC | 84669 |
rs551617625 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60253221 | AAGATGACTCAGACA[C/T]AAACTTAAGTGACCA | 84669 |
rs551622334 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | USP32 | GRCh38.p7 | 17:60369255 | CGCCTCGGCCTCCCA[A/T]AGTGCTGGGATTACA | 84669 |
rs551633554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60238043 | CCAGCAATATATGAG[A/G]GTCCCTAATTTCCCT | 84669 |
rs551660373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186044 | GATGACAGAGAGAGA[C/T]CCTGTCTCAAAAAAA | 84669 |
rs551674408 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258810 | AAACTATGCTTCTCT[A/G]TGATAACTATAATGC | 84669 |
rs551674846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60217830 | ACAACCTTGAACTCC[C/T]GGGCTTAAGAGATCT | 84669 |
rs551686254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423851 | TTCTGAATAGTCATT[A/C]GATGCATGGTTTATT | 84669 |
rs551693839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254450 | TCACTCCTGTAATTG[C/T]AGCACTTTGGGAGGC | 84669 |
rs551711823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60245687 | ACCTCCGTAGGCAGC[A/G]CCAAGGAAGAGAGCC | 84669 |
rs551712113 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60220720 | CCGATCTCGGCTCAC[C/T]GCAAGCTCTGCCTCC | 84669 |
rs551715985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60293331 | CCTGAAAAAGAAAAG[A/C]GTATTAATGTTTTGG | 84669 |
rs551723420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60336453 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 84669 |
rs551731179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60275185 | GTATTGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 84669 |
rs551744500 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60360164 | TGAGCCACCGCGCCC[A/C/G]GCCCTGTAAGACAAA | 84669 |
rs551748320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60386556 | AATCTTCCTTTTCTC[A/G]TCCTGAGAAAATATC | 84669 |
rs551754275 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60401233 | GGCCAAGGTGGGCGT[A/G]GTGGTGGGCGCCTGT | 84669 |
rs551784994 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394090 | GGTGGTTAATTTTAA[C/G]ACCTCAGATTAGCTG | 84669 |
rs551859227 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392840 | CCACCTTCTCCTCCT[C/G]ACCATGCCTCTTGTA | 84669 |
rs551861378 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | CA4, USP32 | GRCh38.p7 | 17:60176754 | TTTTGGCACCAGGGA[C/T]TGGTGTTGTGGAAGA | 84669 |
rs551863903 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60398314 | GGTGGGAGGATCACT[G/T]GGGCCTGAAAAGTAG | 84669 |
rs551868086 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | USP32 | GRCh38.p7 | 17:60206384 | CACTAACCACATCTC[A/G]AGCGCTTAACAGTCC | 84669 |
rs551882400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232163 | TCAACACTAATTTTC[A/T]TTTTCTTTTTTTTTT | 84669 |
rs551885000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60382737 | CTTGTCATCATAAAT[A/G]AAAAGTACATGAAGG | 84669 |
rs551923806 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60390732 | GTCTTTTAATCTAAT[G/T]ACCATTTTATATCCT | 84669 |
rs551951866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60343832 | CGGTCAGGAGTTCAA[A/G]ACCAGCCTGGCCAAC | 84669 |
rs551952627 | snp | C/T | 9.89968e-05 | 0.00703481 | missense | USP32 | GRCh38.p7 | 17:60183380 | GGATCAAAACTTTCC[C/T]GAGGAAATTTGACAA | 84669 |
rs551969601 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60360631 | AGTGAGCTGAGATTG[C/T]ACCACTGCACTCCAG | 84669 |
rs551979382 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60261238 | TTATAGGACTCAGCA[A/T]CTAGAACAGATAGGA | 84669 |
rs551986954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60342892 | TCCTGGGTGAGGCAA[C/T]GCCCCACCCTGCTTC | 84669 |
rs551993013 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60292680 | GATTAAATCACTGAC[A/C]ATTGGTAATCATGAC | 84669 |
rs552001561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60290574 | ATAGCATCCTTTAAT[C/T]GTAATTTCTTAGTGG | 84669 |
rs552034445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235576 | TTTGGCAATGAGTGT[A/G]TATATCAGTTGGCTC | 84669 |
rs552037108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404163 | ACTGCTTAAATGATG[G/T]AATGTAGCAGAAGTG | 84669 |
rs552051135 | snp | C/G | 3.29957e-05 | 0.00406162 | intron-variant | USP32 | GRCh38.p7 | 17:60198468 | ACAAACAAGAGAATA[C/G]AGAGTTCAGAAGACA | 84669 |
rs552054268 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60325212 | TGAAGTCAGCAGTTC[A/G]AGAATAGCCTGGCCA | 84669 |
rs552054677 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60319696 | GAGGTAGGAGGATTG[C/T]TTGAGCCCAGGAGGC | 84669 |
rs552058260 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60289633 | GGCTGAAAAAGAGCA[C/T]CATATGGTTGTTCAC | 84669 |
rs552069633 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | USP32 | GRCh38.p7 | 17:60209684 | TCAACAAATATATTT[A/T]GGATAATCATGAAAT | 84669 |
rs552073666 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60301259 | ACAACGTTTAACAAT[C/T]TGAGGAGCCACCAGG | 84669 |
rs552078762 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411063 | GCCAGGCACGGTGGC[G/T]CACACCTGTAATCTC | 84669 |
rs552079995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60250556 | ATTTTAAAATCCTAC[A/G]TTAATATATTTTAAA | 84669 |
rs552091712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60357380 | ACTGCTTGAGCCCAG[C/G]AGTTGGAGGCTGCAG | 84669 |
rs552106675 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60372051 | GTAGGATTAAGTAAC[-/AG]GGAGAGGGGAAGGGG | 84669 |
rs552113930 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60277542 | CCCTATTGACAGAAG[C/G]CTTTAACATTGTAAA | 84669 |
rs552114029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298792 | ATTATCTTGATTATG[A/G]TAATGGTTTACTGGG | 84669 |
rs552131145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60266682 | TTTTTTTGAGATGGA[C/G]TCTCACTCTGTCGCC | 84669 |
rs552141040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258509 | CTGCATCAGCCATTA[C/T]GATGGATTTAACAGC | 84669 |
rs552142002 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | USP32 | GRCh38.p7 | 17:60385274 | ACCCAAATCCTATAA[A/T]ACAGCCCCATCCCTA | 84669 |
rs552144404 | in-del | -/AC | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60276666 | ATACAGTAAATTGAA[-/AC]ACAGAAAAATCATAT | 84669 |
rs552148254 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296403 | CAGAAAAATAAAGCC[A/G]TGTGTAAGAAAGGCA | 84669 |
rs552173027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411916 | GTTGTTTCCACTTTT[C/T]GGCTATTGTGAACAA | 84669 |
rs552184674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381801 | GAATTTTTAGGGATG[C/T]ATCCAAGGAATTATC | 84669 |
rs552195258 | in-del | -/C | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392481 | GGCGCTTGAGGACGA[-/C]CCCCCCCGCCCCCGC | 84669 |
rs552199582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373693 | TGGCCTCAAATGATC[C/T]ACCCGCCTCGTCCTC | 84669 |
rs552204282 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60312747 | TCCAAAGAACTTGAT[A/G]TCACCAACCTACATG | 84669 |
rs552212493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60381075 | GATTACTGCTGCTAG[C/T]TGTATTCTGTCAGCT | 84669 |
rs552235204 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60382410 | ACCTGAACCACCATG[A/C]CCAGCTAACAGTACC | 84669 |
rs552239601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332270 | GAAAGAAAAAAGTGT[A/G]CAGTCAATCGGTTTT | 84669 |
rs552262091 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245183 | ATGGTATATTTATAC[C/T]GTCTTTTATTATTAC | 84669 |
rs552279526 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60283583 | ATATGAAGCTTGACA[A/C]GGAAAAGTCAAAGGT | 84669 |
rs552289852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265724 | TTTTTATAATTACCA[C/T]AGATTCTCATATATG | 84669 |
rs552304270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363491 | CCACTGCACTCCAGC[C/T]TGGGTGACAGAGCAA | 84669 |
rs552309760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234926 | GCTAGAAAATAATAT[C/T]AAATGCCAGAGTGGA | 84669 |
rs552314558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60230911 | ATTTCTGGCTGCTTG[C/T]GGAAATTTTTGTTTT | 84669 |
rs552316183 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60249162 | TCTCAGCAGTTTACT[A/G]GTTGTGTTTAGCCAG | 84669 |
rs552316268 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60213948 | GTTTTGTTTTTTGTT[G/T]TTTTTTTTTTTAAAG | 84669 |
rs552329831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339766 | AGGAAAATAATTTAG[A/C]AATTTACATTGCTTC | 84669 |
rs552337178 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60185156 | GAGCCAGAAGTTTAA[C/T]CTCTCTTGAAGTTCA | 84669 |
rs552348028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228372 | GATCTATGTCAAAAA[A/G]GAAGTATAAATTAGT | 84669 |
rs552349346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60380512 | AGTTGAGGCTGCAGT[A/G]AGCAGTAAATGTGCC | 84669 |
rs552354912 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60324997 | AACAAGAGCGAAACT[C/G]CATCTCAAAAAAAAC | 84669 |
rs552367769 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60310809 | GGGAGGCCAAGGCAA[G/T]AGGATCACTTGAGCT | 84669 |
rs552367870 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60351680 | TGATCCACCTCCCTC[A/G]GCCTCGCAAAGTGCT | 84669 |
rs552368522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339259 | TATCCTCAAAACAGT[A/G]TGTCTAATGAGATAT | 84669 |
rs552378869 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60191371 | TGCACCACTGCACTG[C/T]AGCCTGGGTGACAGA | 84669 |
rs552390845 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60307891 | TATCAGCAGAAGAAC[A/G]CACAAGTGGCTGGAC | 84669 |
rs552438829 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60285167 | TACCATACAATCACA[A/G]GTAAAAGTGAAAGTT | 84669 |
rs552439567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60226371 | AAACATTCTAATACA[C/T]AGCTATATTTTAATC | 84669 |
rs552453509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60198134 | TTGAATTGTATGCTG[C/T]CTGAGTGGTTCTTCC | 84669 |
rs552466917 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411232 | TGGGGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 84669 |
rs552480649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337729 | AAAAAATAAATAAAC[C/T]GATTAACTGGGCATG | 84669 |
rs552485507 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356542 | GTTCAAGGCATTTTT[A/T]AAAGTCTCTGTCCAA | 84669 |
rs552497282 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60346104 | CAAATCTAATTTAGA[A/G]AATAAGTATAATTTT | 84669 |
rs552505714 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60259494 | CCAGGGTTGGTTCCT[A/G]TCTTGTACCCTGAGC | 84669 |
rs552515569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212564 | GCTCTAAAACCATTC[C/T]TACTCTTCATATTGA | 84669 |
rs552523905 | snp | A/T | 0.0722614 | 0.17581 | intron-variant | USP32 | GRCh38.p7 | 17:60313229 | GCATTCCAGCCTGGG[A/T]GACAGAGTGAGACTC | 84669 |
rs552535377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271335 | AACATATGTAGAAAA[C/T]GGAATGATCCCTACC | 84669 |
rs552569806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204981 | TTTTTTTAGAAGAGA[C/T]GAGGTCTCACTATGT | 84669 |
rs552674996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60321831 | ATGGTCAACTCTATT[A/G]ATCATTAACACCTCA | 84669 |
rs552676194 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60343398 | ATTGACCACATAATT[A/C]GAAGTAAAGCACTCC | 84669 |
rs552706560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330594 | CTCTGTCACCCAGGT[C/T]GGAGTGCAGTGGTGC | 84669 |
rs552719794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60272298 | CACTGACAGAGAAGA[C/T]GGAGTAGGAGTCCCT | 84669 |
rs552727086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60371271 | AAAAAAAAAAAAAAA[A/G]AAAAAAATTAAATGG | 84669 |
rs552735233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60272574 | TAGCACCAGACTTCA[C/T]CTCCTACCACAAATT | 84669 |
rs552779472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288314 | GCATGGTGGCGAGTG[C/T]CTGTAGTCCCAGCTG | 84669 |
rs552843512 | snp | A/T | 6.58946e-05 | 0.0057396 | missense | USP32 | GRCh38.p7 | 17:60226146 | ATTCTATCTTCGACC[A/T]GCTCCATAGGATGGG | 84669 |
rs552846315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281139 | CCTCTATTTGAAAAT[C/T]TGCTTGATCCCAAAA | 84669 |
rs552852946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295924 | AGATAAGGGGGGAAC[C/T]AATGTGTACCATTTA | 84669 |
rs552871660 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409961 | ACAAGCTTGGTTTAA[A/C]ACAAAGATGAAAATA | 84669 |
rs552897992 | in-del | -/ATT | | | intron-variant | USP32 | GRCh38.p7 | 17:60180896 | ATTATTATTATTATT[-/ATT]TTGAGACAGGGACTT | 84669 |
rs552911581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403224 | GGTTTCACCATGTTG[A/G]CCAGGATGGTCTTGA | 84669 |
rs552918943 | snp | C/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423620 | AGGCACGTGCCACCA[C/T]ACTTAGCTGATTTTT | 84669 |
rs552928294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60371950 | AGTAATCAAAACTTA[C/T]TACCTAATTTCAGCT | 84669 |
rs552929675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60189164 | TTGCTAGTGAGCATG[A/G]TCTAGAACATTAGTT | 84669 |
rs552948072 | in-del | -/TTTG | | | intron-variant | USP32 | GRCh38.p7 | 17:60239322 | CTCAGTGTGGATCAC[-/TTTG]TTTATCTTTCTTTAA | 84669 |
rs552953427 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60223893 | GAGCTGGGCTAAGTG[A/G]CTGGGCTTCTACATA | 84669 |
rs552954862 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60348039 | AGGCAGGAGAATGGC[A/C/G]TGAACTCGGGAGGCG | 84669 |
rs552959583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256549 | CTGGGGCCACTATCT[A/G]TGTGGAGTTTGCATA | 84669 |
rs552983077 | snp | A/G | 0.000170486 | 0.00923113 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265368 | TCCCAAATGGAGTAC[A/G]TGATATTTTTAGAAA | 84669 |
rs552987567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271650 | ATATCCAAAATGGTA[C/G]GAAAATTAAACCAAA | 84669 |
rs553007076 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60337603 | CAATTTTGGCTGGGC[A/G]TAGTAGCTCATGCCT | 84669 |
rs553008172 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60220060 | TGAGGAAAAAAAAAA[A/C]CCCTAAGTATTATCT | 84669 |
rs553023126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263664 | TTTTATCTCTACACA[A/G]GGCATTTTCTAACAG | 84669 |
rs553042717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264434 | GAGGCAGGATTGCTT[A/G]AACCCAGGAGGTCGA | 84669 |
rs553047496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416959 | GTCTCAATCTGTCAC[A/G]CAGGTTGGAGTACAG | 84669 |
rs553049045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280639 | AGATACCTTGGCTCA[C/T]TACACAAATTTAAAT | 84669 |
rs553073426 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60226596 | TTTTTATTATTAAAG[A/C]TTACATGGTCAATGT | 84669 |
rs553075135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388380 | CAGAGAAGCAGATAA[A/G]ACAGAAGAATTAAAA | 84669 |
rs553114547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337951 | ATTATCTAATAAAAT[A/G]TTGTGCTATGTACTA | 84669 |
rs553119593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60195377 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTAC | 84669 |
rs553156792 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60234051 | ACCTATCAGGCTCAA[C/G]CAATCCTCCCACCTC | 84669 |
rs553164763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60255579 | CCGGGATTACAGGCA[C/T]CTGCCATGATCTAAA | 84669 |
rs553165584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60207236 | TAGGCGCTTTCATCC[A/G]TAAAACCAACGAGAT | 84669 |
rs553187290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60303349 | CCCTATCACTGGGAA[G/T]AAGGAAGATCAATGT | 84669 |
rs553197252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60368602 | ATTACCAAAAAAAAA[A/C]CCACATACACACAAA | 84669 |
rs553200054 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60233807 | TTTTCTAATTAATAT[G/T]TATTTTCAGAAAGTA | 84669 |
rs553209293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60279184 | TACCTTTAGTACAAA[C/T]GGCTTTAAAGATTAA | 84669 |
rs553216958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403041 | TTTTTGAGACGGAGT[C/G]TCGCTCTGTTGCCAG | 84669 |
rs553222570 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60345759 | GGCCAAGGCAGGCGG[A/T]TCACTTAAGGCCAGG | 84669 |
rs553260023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60385169 | TGAAATTCCTTCTCC[C/T]GGCTCAGAAGCTCCC | 84669 |
rs553263122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60344959 | ACGCACAGTGGCGCC[A/G]GTTAAACATATTATT | 84669 |
rs553264532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424226 | CAACATTGGGGATCA[C/T]GTTTCAACATGAGAT | 84669 |
rs553290361 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60304345 | AGAAAAGATATTTTG[C/T]TTCCCTTTATTTTTT | 84669 |
rs553292989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232322 | GAACTGCAGGCACAC[A/G]CCACCACGCCAGGCT | 84669 |
rs553309087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406086 | CACTTGAGTCCAGGA[A/G]GTCAAGGCTGCAGAG | 84669 |
rs553331370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60247899 | CCGCGTTAGCCAGTA[G/T]GGTCTCAACCTCCTG | 84669 |
rs553340681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60239957 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 84669 |
rs553352293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60253105 | TAAAGTATATGTTTA[C/T]TCATTATCACAAAAA | 84669 |
rs553354032 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60186510 | TGTAACACAGAGTTA[A/T]CAGAATACCAAGTCT | 84669 |
rs553363964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60361716 | ATCTAAGGGTAGCTG[C/T]TTAAATAATGAAGAA | 84669 |
rs553365661 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60217852 | AAGAGATCTTCCCAC[A/C]TCAGCCTCTTGAGTA | 84669 |
rs553374312 | in-del | -/TATT | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177360 | ATTTTATTTACACTC[-/TATT]TATGTACATTAACAT | 84669 |
rs553398826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369422 | TAGCAAGACCCCTAC[C/T]TAAAAAAAAAAAAAA | 84669 |
rs553417369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60252327 | TGTTCCTCAGTAACC[A/G]ATATATTTCAAGTAT | 84669 |
rs553437690 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60218315 | TGTGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 84669 |
rs553473112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60361011 | GCACATGCCTGTAAT[C/T]CCAGCTACAGGGGAG | 84669 |
rs553477811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244127 | TGCAAGCCCCGCCTC[C/T]CGGGTTCACGCCATT | 84669 |
rs553536479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60320240 | AGTCAAGTTCCTGAG[A/G]TATGTTTCTGGTCAC | 84669 |
rs553573660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60319227 | TGTACACTTTAAAAT[A/G]GTTAAAATGGCAAAT | 84669 |
rs553575545 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395428 | ATGGGAATTTTAAGT[A/G]TTAAACCCAGATTAA | 84669 |
rs553585046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60373865 | TTTTTTCTTTATATC[C/T]TTATTTAAAAAGTTT | 84669 |
rs553609390 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60224974 | ATCTGAATTCTTTCT[C/T]AGTATTTTAACAAAA | 84669 |
rs553618939 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60421671 | CTGCTGCCGCGCCAG[A/G]GGCGAGGGTCCCGGG | 84669 |
rs553619750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60381991 | TTTTTGTGTGTATGT[A/G]TGCATGGTGAACTCA | 84669 |
rs553645438 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393834 | GGATTACAGGCATGC[C/G]CCACCATGCCTGGCT | 84669 |
rs553650614 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60214870 | TTTAGGAAATAATAA[A/T]GAGAAATGAGAATTA | 84669 |
rs553692178 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60291685 | GACACACTACTCAGA[C/T]ATTACAGCAGGCAAA | 84669 |
rs553718628 | in-del | -/CT | 0.0399052 | 0.1355 | intron-variant | USP32 | GRCh38.p7 | 17:60293867 | GGGCAGCACTGAGTG[-/CT]GCATGAAAGAATCAG | 84669 |
rs553761806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60191961 | TCCAGCAAGGTCTAG[C/T]AAAGACTATGGTCTA | 84669 |
rs553763416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235107 | TAAGAGTAAGATCTC[C/T]ATTGTGTTCCTACGG | 84669 |
rs553765387 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421502 | CACTGAGTGGGGACA[A/C]CTGGGCCCGGGCCCA | 84669 |
rs553784381 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60357922 | TACAGGCATGTGCCA[A/C]CACACCCAGCTAATT | 84669 |
rs553789576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390326 | TTCTGAACCTTGAAG[C/T]TGTAAATCAGTTTGA | 84669 |
rs553797129 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60190002 | TCTGATTCCCAATGT[A/G]GCGTTGTTAGGAGGT | 84669 |
rs553808406 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60347847 | GTCAGGAAAGGCTGG[A/G]CGCAGTGGCTCACGC | 84669 |
rs553834147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200024 | TATGGTGAAACCCTG[C/T]CTCTACTAAAAACAC | 84669 |
rs553837904 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194095 | TTGCCCAGGCTGGAG[C/T]GCAGTGGCGCAATTA | 84669 |
rs553863434 | snp | A/C/G | 0.000164787 | 0.00907568 | synonymous-codon | USP32 | GRCh38.p7 | 17:60198295 | AGCTTCCTGAGGTGG[A/C/G]AGTGGGCTCGCTAAC | 84669 |
rs553909602 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60207226 | AAGAATGTCTTAGGC[G/T]CTTTCATCCGTAAAA | 84669 |
rs553919128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60182991 | AGATGAGAAAATAGA[C/T]TCAGGGAGGCTGAAC | 84669 |
rs553924921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60365580 | AACTAAAGAATTATC[C/T]TCCCTGTAAGCATTC | 84669 |
rs553926680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60346980 | GGGACACAGTCAGAT[A/G]CAACTCAGATAAAAA | 84669 |
rs553928716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60190805 | CCTCACAATTTGTCA[C/T]GGGCTTCTAACTTCA | 84669 |
rs553941140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60357073 | AGCTGGGACAACAGA[A/G]TAAGACCTTATCTCA | 84669 |
rs553950918 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60262764 | CTGTACAGTCCTATA[C/T]AGTAATAATGTCTTC | 84669 |
rs553978424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298400 | TCTTTTCCAAATTTA[C/T]AGATATCATAATTTT | 84669 |
rs553983734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60266305 | TGTATCTCTAAATCA[C/T]TATTCAGATATAAGA | 84669 |
rs554011206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60242607 | GTAGAGATAGGGTTT[C/T]GCCATGTTGGCCAGG | 84669 |
rs554012629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214311 | GTAACAATAATCTTT[C/G]AAAGATAGTACTGTC | 84669 |
rs554019851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60324918 | TGAGGCAGGAAAATG[G/T]CTTGAACCAAGGAGG | 84669 |
rs554025085 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60241550 | TATTTTTCAATGTTT[C/T]TGTGGAGAGACAGGC | 84669 |
rs554031816 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306533 | ATCCCAGCTACTTGA[A/G]AGGCTGAGGCAGGAG | 84669 |
rs554036979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60205277 | CAGCAACAGATTTTG[A/G]GGACAGGATAAAAAA | 84669 |
rs554049113 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60204439 | GTCCTAAAGGGATCC[G/T]CCTAAACATGCCTGG | 84669 |
rs554053682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60273913 | TGCAGTGAGCCGAGA[C/T]TGCGCCACTGCACTC | 84669 |
rs554056268 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373062 | GTCGCAGCTACTCTA[C/T]AGGCTAAGGTGGGAG | 84669 |
rs554074342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221538 | GAGACGGAATCTCGC[G/T]CTGTCACCCAGGCAG | 84669 |
rs554092183 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406662 | CTGTGATTACAGGCA[A/C/T]GCGCCACCACGCCCA | 84669 |
rs554108318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412362 | ATACAAAAATTGGCC[A/G]GGTATGTGATGTGAA | 84669 |
rs554126035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60283221 | TAGTGTAGCTATAAT[A/G]TAAAAGTTCATGGTG | 84669 |
rs554153429 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60373438 | ATTAATTTTAGCTTA[C/G]TGTAATTTTTTTTTT | 84669 |
rs554156665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60323789 | AAGAAGGAAGACTGG[A/G]AAAGTAGTTCAAGAT | 84669 |
rs554167157 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419328 | TGAGAACACATGAAC[A/G]CGTAGAGGGGAACAA | 84669 |
rs554168265 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60235493 | CTACCAATATTCTGA[C/T]AATAAGCAGTGACAG | 84669 |
rs554209610 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60237374 | TGGTCTTGAACTCCC[-/A]AAAAGTGTTGGGATT | 84669 |
rs554221285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60397643 | CTGGGATGAGACACC[A/G]TGCATAGTCACCCCA | 84669 |
rs554224179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60307380 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 84669 |
rs554238268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60282323 | CTTTAAGTGTGTAAG[C/T]ATCATAATTCATTTC | 84669 |
rs554244599 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412892 | GGAAATCATTAGGCC[C/T]CAGCAATTTTGACAA | 84669 |
rs554257990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190247 | TTTGCCAGAAGCCAG[G/T]ACCATGTCCTTGAAC | 84669 |
rs554262521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60182435 | TGTGAGAGAATAAAA[A/G]TGAAAAGGCACATAT | 84669 |
rs554273745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403283 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCATG | 84669 |
rs554282025 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419626 | TAGTCCCAGCTACTC[G/T]GGAGGCTGAGGCAAG | 84669 |
rs554299633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289718 | TTTCTAAGCAGAAAA[A/G]GGGAGAAGCAATTCA | 84669 |
rs554309811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289031 | TTGTTTGTTTGAGAC[A/G]GAGTCTCACTTTGTC | 84669 |
rs554317882 | snp | C/G | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424182 | GATCCACCCCCATGA[C/G]CCAAACACCTCCCAT | 84669 |
rs554319772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360385 | TTTTGTATTACAGGC[A/G]CAGTGGCTCATGCCT | 84669 |
rs554327517 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60332373 | TTACTCTGGGCCGGA[C/T]GCGGTGGCTCAAGCC | 84669 |
rs554329410 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266255 | ATGTCATTATAGTCC[A/T]CAGAACTTGTAGGAC | 84669 |
rs554332221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404499 | CCAGATTTCTACAAG[A/G]AGACAATCTCGTTTC | 84669 |
rs554344189 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60249990 | ATAGTAGAGGCAAAA[A/T]AAAATAAAACTGAAA | 84669 |
rs554361141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315817 | CTGAAGAATAAGTAA[A/G]TAAGTCTCTATAGCA | 84669 |
rs554364711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403660 | TATTTAAGGAAAGGG[A/G]GTCGTGATGTATTGA | 84669 |
rs554368887 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411420 | AGGAGGCTGAGGTGG[C/G]AGGATCACTTGAGCC | 84669 |
rs554370303 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232369 | GTAGAGTCGGGGTTT[A/C]ACCATGTTGGCCAGG | 84669 |
rs554374573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197692 | TCCCAAAAATTATTC[A/G]GAGTAAATGCATTTA | 84669 |
rs554401362 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60363639 | CCATAGGTCCATGCC[A/C]CCATGCCCAGCTAAT | 84669 |
rs554404650 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60263023 | GTGTAATCATGGCAC[A/G]CTGCAGCCTTGACCT | 84669 |
rs554461914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388627 | CCTTAGAAAACACAC[A/G]CAATATAAACAAGAG | 84669 |
rs554463582 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424389 | CCCAAGGAGCTGCTT[A/G]AATCTTTTGATGCCT | 84669 |
rs554471092 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60257833 | CTATTCTGCAAACTC[A/T]AGGAGTTCTGCTGGT | 84669 |
rs554486353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234966 | ATGTAGATTCTCCCA[A/T]GTATACCTCTCCCTT | 84669 |
rs554498669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60396428 | TCCATCAGTACACAA[A/G]TATATAATGTAAAAG | 84669 |
rs554498721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234679 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 84669 |
rs554501643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410682 | CAAAAAATAAATAAA[G/T]AAAGAAAGAACTAGA | 84669 |
rs554524935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60282253 | TATCTGATATCATTT[A/C]GCTAACCAAAAGTTT | 84669 |
rs554560679 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60260850 | AGAATAGTATATCTT[-/C]CCCTCTAACATCCAT | 84669 |
rs554576994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60198606 | CTTTATTGACACAAA[C/G]AGAACGGTTACAGTG | 84669 |
rs554577511 | snp | A/C | 2.57463e-05 | 0.00358783 | intron-variant | USP32 | GRCh38.p7 | 17:60207148 | CTACAGAAACAGAAG[A/C]AAGATGAGAAGGGGG | 84669 |
rs554588495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289609 | TAAATCTCTGGAGAA[A/C]AGTATCCAGGCTGAA | 84669 |
rs554602238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60357845 | GCAATCTCAACTCAC[C/T]GCAACTTCCACCTCC | 84669 |
rs554613915 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60194334 | CAGGCGTGAGTCACC[A/G]CACCCTACCCCCTGC | 84669 |
rs554618947 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404381 | GTTTTTTTTTAATGT[A/G]ATGCACATGGAAGAG | 84669 |
rs554631871 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60320721 | ACACAGTTATATAAA[C/T]CTATTTAGTAATCAA | 84669 |
rs554651188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347791 | AGTACCGAGAAACTT[C/G]AAGGATTATGTTATT | 84669 |
rs554652636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373318 | AGGGGTGAGTCAATG[C/T]TGAAGTCCTAGCCCT | 84669 |
rs554676300 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60364902 | TATATTTTAGACCCA[A/T]ATTTTATATTTGTAA | 84669 |
rs554681334 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60315145 | GCTCACGCCTGTAAT[A/C]CTAGCACTTTGGGAG | 84669 |
rs554688576 | snp | A/G | 1.65362e-05 | 0.00287538 | intron-variant | USP32 | GRCh38.p7 | 17:60214823 | CAGATGTGAAAAAGA[A/G]GCACCCCTCTCAGCA | 84669 |
rs554691150 | in-del | -/A | 0.44252 | 0.159487 | intron-variant | USP32 | GRCh38.p7 | 17:60203396 | CAGAGCGAGACTGTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs554694784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60206155 | GAAAACCCATCTCTA[C/T]AAAAGATACACCATA | 84669 |
rs554708882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214237 | GTGAGCCACTGTGCT[C/T]GGCCACACCATTAGT | 84669 |
rs554733567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60324733 | ATAGGCCAGGCATGG[A/T]GGCTCACATCTGTAA | 84669 |
rs554741909 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60363542 | AAAATTTGAGACAGG[G/T]TCTCACTCTGTCGCC | 84669 |
rs554774475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60323576 | AAAAGCCACTGAATT[A/G]TATACTTTAAATGTG | 84669 |
rs554778644 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60363132 | CCATCTCTATTTTTT[A/T]AAAAATATTAAATTT | 84669 |
rs554798027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249746 | ATATTTGGTCAGTTT[C/T]CAGAGTCCTGAAATG | 84669 |
rs554864236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60182894 | ACCATTCCTGTTTAC[C/T]GTATATCAGGCACTG | 84669 |
rs554882649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60220937 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCAACAC | 84669 |
rs554889204 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60375597 | CTTTTTCTGGTGTTT[C/T]GTTGTTGTTTGTTTG | 84669 |
rs554889423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211813 | AAAACATATAAATTA[C/T]TTAATTGCAGAGTTA | 84669 |
rs554889429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60219958 | GATCTGATTACTGTT[A/G]AAATTCCTGCTCCGA | 84669 |
rs554890620 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60227825 | TTGTCTGTTACCACT[-/G]GCTTCACTTTAGTAG | 84669 |
rs554895288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231786 | TGTAATAATGATAGA[A/G]AAGATTTCACCATTC | 84669 |
rs554897444 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60321987 | TGGCATTCAATGACT[A/G]TTGAGAAAACTTAAT | 84669 |
rs554948915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330995 | AAGCTAGTCATATAC[C/G]TAAATTCCTACAATT | 84669 |
rs554958558 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60238355 | TTGGTTTTAAAAATA[A/G]TATCTCTTGATGTAT | 84669 |
rs554960721 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60300863 | TCCCTCTCACCTGAT[A/G]CCTCCAGCAACCACT | 84669 |
rs554990510 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393064 | ATTGCCACGTCCCAT[A/T]TCCCACCGTTTTTCA | 84669 |
rs555002721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60351948 | TTCACCTGGCAAAAA[A/G]AAACGCAAAGGGCTA | 84669 |
rs555038249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190186 | TCTTGCCTGTGTCTG[G/T]TCTCCTTTGATCTTC | 84669 |
rs555056151 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60196900 | TTAAATTTAAATCTG[G/T]CCAGGTGTGGTGGCT | 84669 |
rs555062943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274447 | CAGAAGTTCAATGAA[A/C]CTTGTGTTAGAAAAC | 84669 |
rs555088639 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60343155 | AGATTCATAAAGCAG[G/T]TCCTTAGAGACCTAC | 84669 |
rs555095886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297815 | TTGAATAAGCACTGG[C/T]CTTGAGATAAGCAAT | 84669 |
rs555098820 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60286026 | CTGTAATCACAGCTA[C/T]TTGGGAGGCTAAGGC | 84669 |
rs555139137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60351228 | GCACAAGGCAATCAG[G/T]CACCAATCTACCACC | 84669 |
rs555152236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257249 | TGGATTCTGGGATTG[C/G]CAGATGACTGGTAGA | 84669 |
rs555156812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305520 | TTTGGAGGGGACAAA[C/T]ATCCAAACTATATCA | 84669 |
rs555164973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418610 | AATTTTGCAAACTAT[A/G]CATCCTACAAAGGTC | 84669 |
rs555173536 | in-del | -/TTTAG | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60365047 | AAATTCCTTATGCCT[-/TTTAG]TTAAGAAATCATGTT | 84669 |
rs555219116 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60236994 | ATCCATCCAACACCT[-/A]AAGAACATTTGAAAC | 84669 |
rs555231318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60209231 | GCATAAGAATTAAGC[A/G]CAGAAATAGAAATTC | 84669 |
rs555236440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60313107 | AATACAAAAATTAGC[C/T]AGTCATGGTGGCAGG | 84669 |
rs555243533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60208314 | TATAATAGCAAATAT[C/T]TCAGCCTAGAATTTT | 84669 |
rs555246449 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60379761 | ACGTATAAATGAGAG[A/C]AAAAGGTTATGGCTT | 84669 |
rs555247209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216530 | CCACTAAATAAAGCT[A/G]AGAAAATATGTGCAT | 84669 |
rs555271565 | snp | A/C | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264353 | GAGACCTGGTCTCTA[A/C]AAAAAAAAAAAAAAA | 84669 |
rs555291510 | in-del | -/AG | | | intron-variant | USP32 | GRCh38.p7 | 17:60335886 | CAGCTAAATTTTGGC[-/AG]AGTCTGTAACACTGC | 84669 |
rs555292697 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60388467 | CATCTTTCACCGAAC[C/G]GTTTTTGAATGCTGT | 84669 |
rs555300517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200941 | CTCAGCTCACTGCAA[C/T]CTCCACCTTCTGGGC | 84669 |
rs555309281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60215735 | AAATAGGTATAGACT[C/T]TACATAGCCAAACAG | 84669 |
rs555339672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60367013 | TTTATAGTTTTAGTA[A/G]AGACGGGGTTTCACC | 84669 |
rs555368114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60309494 | GTAATCACAGTTACT[C/T]GGGAGGCTGAGGTGG | 84669 |
rs555375889 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178175 | ATTTCATTAAATACA[C/T]TTATGAACTCCTAAT | 84669 |
rs555378116 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60375814 | GGTTTCACCATGTTG[G/T]CCAGGGTGGTCTCAA | 84669 |
rs555391757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194367 | TTTGTATTCTCATAC[G/T]TTCCAGAACCTGGAG | 84669 |
rs555408864 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60317352 | GACCTCATCTCTATT[A/T]AAAAAACTTAAAAAT | 84669 |
rs555422688 | in-del | -/AAAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60386380 | AAAAAAAAAAAAAAA[-/AAAA]TCCCTCCACCACTGC | 84669 |
rs555428483 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60386242 | CCAAAAAGCAAAAGC[-/AGA]AGCATAAACAAGCTC | 84669 |
rs555435065 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60259241 | AAAGACCAACCTGCG[G/T]TCTCTTTAGTTTACT | 84669 |
rs555453484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185768 | CTATATAAGGAAAAA[A/G]AAAATACAACTGGCT | 84669 |
rs555454722 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60201407 | TCTTGGGTGGATACC[A/T]ACAGGTAGAACTGCT | 84669 |
rs555461393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60287726 | CCTAGGAAACTAATA[C/T]AGCTTCATTAAGGAC | 84669 |
rs555465104 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60184724 | CTGAGGCAAGAGAAT[C/G]ACTTGAGCCCGAGAG | 84669 |
rs555489676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333524 | AGAGTCACTTGAACC[C/T]GGGAGGTGGAGGTTA | 84669 |
rs555497461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407161 | CTGAGGACGCACAGA[C/T]TGGAGTTCATGGAAC | 84669 |
rs555503529 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408331 | AGATGGAACTTCTAG[C/T]GGTGAAAAATACAGT | 84669 |
rs555519934 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60357287 | GAGACCCCATCTCTA[C/T]AAAAAATAAATAATA | 84669 |
rs555524432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407699 | AGGCAGAAGAATTGC[C/T]TGAACCCAGGAGGCG | 84669 |
rs555563084 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415055 | GTTTATAGTCCTCTA[A/T]AAAGAAAATAAATTT | 84669 |
rs555572045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60291774 | ACTAGAGGTATCTAA[C/T]AGTTCAAATAGCCAT | 84669 |
rs555601115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60284170 | AGGTGAAACAATCAA[C/T]GTACAGGAATATTTG | 84669 |
rs555611326 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60362983 | TTGCATCTAATCCAG[C/G]ATTTTACTCTTTAAA | 84669 |
rs555621374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60230010 | GTGGAGACAGGGTTT[C/T]GCCACGTTGGCCAGG | 84669 |
rs555633592 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60399533 | CTGGGTGTGGTGGCA[A/T]GTGCCTGTAGTCCCA | 84669 |
rs555634429 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423106 | CTGAGAAGCTTTTGA[A/T]AGGTGAGGGGCAAAT | 84669 |
rs555647477 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60299241 | CTCAATAAAACTTTT[A/C]TTAAAAATGATCTCT | 84669 |
rs555665946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413152 | TTTGAAAACTATTTT[A/G]GGAGAAGCAGGAGTT | 84669 |
rs555675519 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60261563 | AGGCAGGAGCATCAC[C/T]TGAACCCAGGACGTA | 84669 |
rs555695155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400244 | TTCTGAGATTACAGG[C/T]GTGAGCCACCAAGCC | 84669 |
rs555698324 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60222953 | TCCCAAAGTGCTAGG[A/T]TTACAGGCATGAGCC | 84669 |
rs555727132 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60189152 | AATTTTCCCTCCTTG[C/T]TAGTGAGCATGATCT | 84669 |
rs555746193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244898 | TGGCCTCCCAAAGAG[C/T]TGGGATTACAGGCGT | 84669 |
rs555755198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295491 | TTAAATGGAAATTTC[C/T]AGAAATGAACAATTC | 84669 |
rs555779026 | in-del | -/T | 0.27008 | 0.249192 | intron-variant | USP32 | GRCh38.p7 | 17:60351440 | ACTATGCCAGGCTTC[-/T]TTTTTTTTTTTCGAG | 84669 |
rs555783438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60260826 | TTTCTCCTACACTTG[A/T]TAGTAGTCAGAATAG | 84669 |
rs555783731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267890 | ATCTTGGCTCACTGC[A/C]ACCTCCACCTCCCAG | 84669 |
rs555787555 | in-del | -/AGATCACCAA | 0.0019968 | 0.0315343 | intron-variant | USP32 | GRCh38.p7 | 17:60292035 | CAATGACCTACCTGC[-/AGATCACCAA]ATTTAATGATCACTT | 84669 |
rs555790580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228962 | GTGAGCCACCTCACC[G/T]GGTTAAATTAGGTTT | 84669 |
rs555840926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384296 | TAGCAAATGTTAAAA[C/G]GCTTTTGCCACAGGG | 84669 |
rs555845032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267483 | ACCTTTCCAGTATAA[A/C]TAATGTACATTCAAT | 84669 |
rs555877312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60383332 | GTATAACTCGATTCC[G/T]GTCTTTATTTTTTAC | 84669 |
rs555877680 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60392062 | GCCCCCACCTCCCCC[C/G]ACACTAACAAGTGCG | 84669 |
rs555914280 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60391466 | CTCGTCCCCTTCCAG[C/G]TAAGGCTGTTAGGAA | 84669 |
rs555919911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60253265 | CTGATTATGAGATAA[A/G]GAGTACACTGAATAT | 84669 |
rs555922743 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60292829 | TCTACTCAAAACCTT[A/C]CAGTGGTTTCTATCT | 84669 |
rs555937326 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60293164 | CTTTATTCTACTTTA[A/T]TTTCCCCTATAGCAC | 84669 |
rs555940141 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60366968 | AGCTGGGACTACAGG[A/C]GCCCGCCACCACACC | 84669 |
rs555945899 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388325 | ACACACACACACACA[C/T]CGCCTTATAATCCTG | 84669 |
rs555951155 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60236693 | ATCAGTTTGAGAACA[G/T]TTAAAACATTTCAAT | 84669 |
rs555952118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60340544 | TTTCTCCATCCCTTT[A/G]TTTTGAGCCTATGTA | 84669 |
rs555964328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192437 | TGACCTCAAAAGGAA[A/G]TGAAAAATATTTTTT | 84669 |
rs555967587 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60394296 | GGGCCCAGCTGTGAG[A/G]GAGAAAAACCCTCAA | 84669 |
rs555971514 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60334226 | TTATGGTTTAATATT[G/T]CATTTTCTGTTTGCA | 84669 |
rs555977020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375666 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 84669 |
rs555977327 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP32 | GRCh38.p7 | 17:60366168 | TCTTTTTTCTTTTTT[C/T]TTTTTTTTGAGACGG | 84669 |
rs555987019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348592 | CCACCCTAGGCAACA[C/T]AGTGAGACCCTGTCT | 84669 |
rs555992555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200127 | TGAACGCAGGAGGCA[C/T]AGAGTACAGTGAGCC | 84669 |
rs555992874 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60225312 | ACACACAAAAAATGG[C/G]TGGGCATGGTGGCGC | 84669 |
rs556004118 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60397507 | GCTGGAACTACAGGT[A/G]CACACCACCACACCT | 84669 |
rs556008116 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60361199 | CTACCATAAAATCCT[A/C]CTTACTTCCTCCCCT | 84669 |
rs556012379 | snp | C/T | 6.60633e-05 | 0.00574694 | intron-variant | USP32 | GRCh38.p7 | 17:60236088 | TGGCTGGAAGTCTCA[C/T]GCAGCTGAAAATCCT | 84669 |
rs556014803 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414138 | GAGGCCATGGTGGGC[A/T]GATCACTTGAGGTCA | 84669 |
rs556016642 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60244041 | TGTGTTTTTTTTTTT[G/T]TTTTTTTTTTTTGAG | 84669 |
rs556059895 | snp | C/T | 3.56538e-05 | 0.00422204 | synonymous-codon | USP32 | GRCh38.p7 | 17:60208170 | ATCCATATTCAGTCT[C/T]AGTCCATACCGTACA | 84669 |
rs556073234 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60224439 | AGAAAATGCTAGCTC[G/T]GTCCAATTTGCTTAC | 84669 |
rs556076694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317908 | GAGAATCACTGGAAC[C/T]CAGGAGGCAGAGATT | 84669 |
rs556082820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214984 | TTGTTTGTTTGTTTT[G/T]AATAGATGGAGTCTT | 84669 |
rs556083082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222708 | TTTTTTTGAGACGGG[G/T]TCTTGTTCCGTCACC | 84669 |
rs556129073 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60243415 | TAAGTGCGGCAAAAG[A/C]AAGTATCCTTTCCTG | 84669 |
rs556140074 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60341117 | ATTTTTTCCTTCATT[G/T]CAACCTTAGTGAATC | 84669 |
rs556144258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332511 | AAATTAGCTGGGCGT[G/T]GTGGTGGGCGCCTGT | 84669 |
rs556156051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267452 | AGCTGATATAAAGAC[A/G]GTCCACTTCCATGTT | 84669 |
rs556173832 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60342212 | TCCACTCAAGACCTT[C/G]TTTGCCTGGGTATCA | 84669 |
rs556175418 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60259393 | ATGTAAAAAAACAAA[A/G]AAATGAAAAAATTAA | 84669 |
rs556176554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60316369 | GGGAAAATGGGGAAC[A/G]GAAATCAGGTATAGG | 84669 |
rs556194253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60226338 | TTAAGTCTCCTGTGG[C/T]TGGCCACAGACATTT | 84669 |
rs556196900 | in-del | -/TTG | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60312409 | TCAATACTTTTCCAT[-/TTG]TTGTTGTTGTTGTTG | 84669 |
rs556218473 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP32 | GRCh38.p7 | 17:60200770 | TACAGTTTTATATCC[C/T]ATGCACAAGTAAATA | 84669 |
rs556230610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60209041 | ATTAAAGTTATTTGT[C/T]CATTAACAAGTATAA | 84669 |
rs556249045 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60267818 | CCACCGTGCCAGGCC[-/T]TTTTTTTCTTTTGAG | 84669 |
rs556275834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317031 | AGGTTATCAGGGGCT[A/G]GGGAGGAAGAAGAAT | 84669 |
rs556278904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60340253 | TTCCATGAGTCTATC[C/T]ACCCACTAAAACTAA | 84669 |
rs556282663 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395542 | TAAGTCTAATAACGT[A/G]GAAAGTCTGAAGTCT | 84669 |
rs556298915 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60303316 | AGGAAAACATAATGG[A/C/T]CCCAGACCTTACAGA | 84669 |
rs556347026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308629 | ACTGGATAACTATAC[A/G]CAGAAAAATAAAACT | 84669 |
rs556359634 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422475 | GCCGTGGCTTTGCTC[C/T]GAGTTCTGGAGCCAA | 84669 |
rs556367304 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60309417 | CCAGCCTGGGCAACA[G/T]GGCAGAAACCCCTGT | 84669 |
rs556371022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190858 | CTTATTAATAATTAG[C/T]ACAGTTTCAGGGAAT | 84669 |
rs556403847 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60253177 | AAGGCAATACCAAAA[C/G]TCAAAATGCTATACT | 84669 |
rs556415638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235920 | ATATTATCTTTTTTT[A/G]GGGTTGTTGCAAGGA | 84669 |
rs556442307 | in-del | -/CAGCACTGAGT | 0.0399052 | 0.1355 | intron-variant | USP32 | GRCh38.p7 | 17:60293855 | CCAAAAGAAAATGGG[-/CAGCACTGAGT]GCTGCATGAAAGAAT | 84669 |
rs556449295 | snp | C/G | | | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402465 | CACGTTGCCCAGACT[C/G]GTCTTGAACTTGGTT | 84669 |
rs556455681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348527 | TACCTATAATCCTAG[C/T]ACTTTGGGAGGCCAA | 84669 |
rs556488648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60324991 | CTGGGCAACAAGAGC[A/G]AAACTCCATCTCAAA | 84669 |
rs556496176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60357780 | TTTAGATACTTTTTT[C/T]TTTTTGAGACGGAGT | 84669 |
rs556498759 | in-del | -/AGA | | | intron-variant | USP32 | GRCh38.p7 | 17:60299455 | ATGCAAGAGGGAGAG[-/AGA]AGGAGGCTGAATTCT | 84669 |
rs556516660 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60299143 | TCTCTCCTCTGTCCC[C/T]TATCCCCTCCAAAAA | 84669 |
rs556542229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337910 | AAGATTAGACAAGAC[A/G]TACATGAACAATTAG | 84669 |
rs556542470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60328814 | CACCTGGTCCAGCTG[C/T]AGCCTTGCAGGAAGG | 84669 |
rs556567692 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60401751 | AAAAGAAAGAAAGTA[-/G]ATCTCTGCCTATGCA | 84669 |
rs556572124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412239 | CCAGGTGTGGTGGCT[C/T]ATGCCTATAATCCCA | 84669 |
rs556586345 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60206025 | CCAGATGTTGCATTT[A/G]AAATTTAAATTAGGC | 84669 |
rs556642349 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60274956 | AAAGATACTCCTCTA[C/T]CCCTCTTCCCTGCTC | 84669 |
rs556654130 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417191 | CCAAAGTGCTGGGAT[C/T]ACAGGTGTGAACCAC | 84669 |
rs556658241 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60371396 | ATGTGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 84669 |
rs556659526 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60311588 | AACACTTTGGGAGGC[C/T]GAGGATGGTGGATCA | 84669 |
rs556665486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60263918 | CTCTATTTAATAACA[C/T]CATTGTGGTGTAGAT | 84669 |
rs556713394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235289 | TTCTCATTTTTCTAC[C/T]TACACATACCATCAT | 84669 |
rs556720852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378721 | TTTACATGAAGTATC[C/T]AGAATAGGCAAATTC | 84669 |
rs556732377 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423525 | TGGAGTGCAGTGGCT[-/C]CAGTCTCGGCTCACT | 84669 |
rs556754194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289768 | TACAACCTGAACTAT[C/T]TGATCAGGAAAAAAA | 84669 |
rs556799733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60251985 | ACAAATATCACTGTG[C/G]GCATATGTTTATATG | 84669 |
rs556800048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60242691 | GGATTACAGGCATGA[A/G]CCACCACGCCTGGCC | 84669 |
rs556815418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60304201 | TTACATTAAAAAAAA[A/C]CCAAAAATTATAGCT | 84669 |
rs556842181 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60397823 | AGATGGGCCTGCCTA[C/T]GTATAGGTATTTAAT | 84669 |
rs556842214 | in-del | -/AAAG | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60390542 | TGTTCCACAAGGGAA[-/AAAG]AAAGAAAGACATAAA | 84669 |
rs556844334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411644 | CCTCCAGAGTAGCTG[A/G]GATTACAGGCATGCA | 84669 |
rs556847126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60365413 | TTGAACACAGAAGGT[A/G]AAGGTTGCAGTGAGC | 84669 |
rs556853861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60303287 | CAAAAACACCTTTAT[C/T]CCTGGGGAAGGGCAG | 84669 |
rs556881786 | in-del | -/TA | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60200763 | TTTTCTTTACAGTTT[-/TA]TATCCTATGCACAAG | 84669 |
rs556887699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404604 | ATCTTTGTATGACCT[A/G]CTACACTAAAGGCAT | 84669 |
rs556898354 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | USP32 | GRCh38.p7 | 17:60267512 | ATCTTTTTTTGGCAA[A/C]AACAATTTTAACTCT | 84669 |
rs556900508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60344375 | CCTCGTGATTCACCC[A/G]CCTCGGCCTCCCAAA | 84669 |
rs556901137 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415996 | AGGCACGTGCCACCA[C/T]GCCCAGCTAATTTTT | 84669 |
rs556923867 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60228037 | CAAAATTCTTTTTTT[-/C]TTTTTTGAGACAGAG | 84669 |
rs556938015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424138 | CTCACTTAATTGGGG[C/T]AGGGAGGGCACCAAG | 84669 |
rs556940259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60314029 | TGCTCAAGAATTTAA[A/G]CAAAAATAAAAACAT | 84669 |
rs556977646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60180011 | GAAGATAGGAGTTTT[C/T]GCATTAACTAACTCC | 84669 |
rs556981198 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60351952 | CCTGGCAAAAAAAAA[C/T]GCAAAGGGCTATTCT | 84669 |
rs556983246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271563 | GATAATATATCTTCC[A/G]CAGATATATTTTAGT | 84669 |
rs556999108 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60221426 | CTTTTTAGAAGTTAA[C/T]GTACCATATCTCATC | 84669 |
rs557002777 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415568 | ATTCACTGGATAGCA[C/T]TTCAAAGGTTTGTTG | 84669 |
rs557002845 | in-del | -/TTTTCTTTTTTTTTT | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60376527 | TTTCTTTTTTTTTCC[-/TTTTCTTTTTTTTTT]GAGACAGAGTCTCAC | 84669 |
rs557025977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60310345 | GAATTAACCTAAGTG[C/T]CCATCAACAGATGAA | 84669 |
rs557034444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387753 | ATACACCAAATTTAC[C/T]GAACATAACTTAGCC | 84669 |
rs557035072 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60237386 | TCCCAAAAGTGTTGG[C/G]ATTACAGACATGAGC | 84669 |
rs557043000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60287815 | AAACAAAACACTGAC[A/C]AAAAAAAAATTTCTC | 84669 |
rs557044788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60270981 | GAGGCACCCTACTGG[A/T]GGAAGAGACGAGGTC | 84669 |
rs557047708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60201554 | AGTTCCTGTTGCTCT[A/G]CTTAGCAACCCTGTC | 84669 |
rs557049630 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60216293 | CAAAGAGAGGTGGCA[-/A]AAAAAAAAAAAAACA | 84669 |
rs557051356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233295 | GCATAGTGAGACCCC[A/G]TCTCTACAGAAAATC | 84669 |
rs557055378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60279736 | CAGCAAGTTGGGAGG[C/T]TGAGGTGGGGGGATC | 84669 |
rs557069237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387148 | ATTTCCGTGTATAGA[A/G]TGATACATTATGCTA | 84669 |
rs557081953 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393647 | ACCAACAGATTCTAA[C/T]ATACCCTGCTAGAGA | 84669 |
rs557086358 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418678 | CAAGAATAAAAACAA[A/C]CAACCCCATTAAAAA | 84669 |
rs557087834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254973 | ATAATAATCTACATC[C/T]CACTTTCCTATTTCC | 84669 |
rs557096524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60344916 | CAAGCCTCCTATTTC[A/G]GCCTCCTGAGTAGCT | 84669 |
rs557124420 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60279215 | CTTGTCATTAATCCT[A/G]TTGACTGGGCACAGT | 84669 |
rs557132028 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60251282 | CTTCACTTAAAAAAA[A/T]AATAATAATAATAAA | 84669 |
rs557132733 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60348515 | TGCAGTGGCTCATAC[C/T]TATAATCCTAGCACT | 84669 |
rs557147127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60262324 | AGCCTCCTGAGTAGC[C/T]GGAATTACAGATGCC | 84669 |
rs557161552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210350 | AGAGTCTTACTCTGT[C/T]GCCCAGGCTGGAGTA | 84669 |
rs557167707 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424402 | TTAAATCTTTTGATG[A/C/T]CTCATTGTTCTCATC | 84669 |
rs557175878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60377028 | TATCCAAAGGGCTAC[A/C]TTTGAGGGGTTATAT | 84669 |
rs557181227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60277448 | GCCTTGCATCACTAA[A/C]GGATAAGAGGATAAT | 84669 |
rs557193313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60276512 | CCAAGTAGTAGATCA[C/G]CATACAAAAAAATCT | 84669 |
rs557217555 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227061 | AAAAAAAAAAAAAAA[-/T]CATATTTTTTTCTTT | 84669 |
rs557228012 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60316082 | CTTCCAGAATACAGT[C/T]ACTGGTGCTCTGCAG | 84669 |
rs557241174 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60383557 | AAACTGTTCAGAATA[C/T]TGCACAATAGTGATA | 84669 |
rs557246285 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392303 | TCCCGGTAACGGCCG[A/C]CCAGGGCCGCACGCT | 84669 |
rs557263626 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60355910 | AAAAAAAAAAAAAAA[-/AA]GCAGTATTTGTGGTG | 84669 |
rs557291045 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60389416 | GGAGTGGTGGCATGC[A/G]CCTGTAGTCCCAGCT | 84669 |
rs557295973 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60212823 | CAGTGATGTGATCTT[A/G]AGTCACTGCAACCTC | 84669 |
rs557297294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210663 | TGAAAATGGATTGGA[C/T]TGGATGTAATTAATA | 84669 |
rs557301587 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60241060 | TGGAGTGCAGTGGCT[A/C]AATCTCAGCTCACTG | 84669 |
rs557324879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60247400 | GGTCAGGCTGGTCTC[A/G]AACTCCTGGCCTCAG | 84669 |
rs557333144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60262910 | TCAAAGTTCAATTTA[C/T]ATGGTTCCCTTTCTA | 84669 |
rs557334577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60344831 | CAAAATAGTAAACTT[C/T]TATTTTATTTTTTTT | 84669 |
rs557354707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232355 | TTTTTATATTTTTAG[C/T]AGAGTCGGGGTTTCA | 84669 |
rs557362491 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177224 | TTGTATGAGGAAAAA[C/T]GGCACATGGAGGCAT | 84669 |
rs557389200 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377867 | AATTTCATGGTTATA[C/T]CCTTTGCACAATCTG | 84669 |
rs557392093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60360950 | CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC | 84669 |
rs557403040 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP32 | GRCh38.p7 | 17:60326461 | GATTACAGGCACCGA[C/T]AACCATGCTCGGCTA | 84669 |
rs557427927 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60180210 | TTTGTATTTTTAGTA[A/G]AGATGGGGTTTCACC | 84669 |
rs557431710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327871 | GTATGTGGACACTCA[C/G]GGCGGTGCTGACGTG | 84669 |
rs557439661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60179817 | CTGGGACTACAGGTG[C/T]GTGCCACCACGCCTG | 84669 |
rs557442387 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60307101 | ATTTTTTTTCCTTTC[-/T]TTTTTTTTTTTTTCT | 84669 |
rs557465839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231857 | ATAAAGCTTGACACA[C/T]TAAAGCGGGGAAAGA | 84669 |
rs557467766 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296047 | TCATGAAAGTGGTAA[A/C]CTCTGTAGAGGGAAG | 84669 |
rs557473407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218180 | ACGAGGTCAGGAGAT[A/C]GAGACCATCCTGGCT | 84669 |
rs557474140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60335998 | TCCCAACTGTTTTTA[C/T]CGTCTACTACACTAG | 84669 |
rs557484850 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60251455 | AACTCCCATCTATCC[A/C]GAAACCCAAGCCAGA | 84669 |
rs557515317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60385921 | CCCTAATAAAGAGGG[A/G]TGTTAAGGAAAGGTC | 84669 |
rs557520354 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60327531 | CCAGGCTGAGCCCGC[A/C]CGCCAGCAGAAGAGC | 84669 |
rs557528288 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60301835 | TTAGTGAAATCATGT[C/T]AAGTTTCTCCCTCTT | 84669 |
rs557534718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60217769 | AAGAGACAAGCTCTT[A/G]CTCTGTTACCCAGGC | 84669 |
rs557536132 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178110 | CAAAATAAAAAAATT[A/G]GTGGACATGCAAACA | 84669 |
rs557548798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60352044 | TATGATATAAATGGA[C/G]TACAGGGTATAAGAA | 84669 |
rs557550233 | snp | A/G | 0.000107381 | 0.00732658 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231648 | ATGGGAGAGAGGCAC[A/G]AAAGGTGATTTAAAG | 84669 |
rs557559381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60202246 | GGTTTCTGGGCTCTC[C/T]ATTCTATCCCAATGG | 84669 |
rs557586375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186356 | AGTATGCTGCAGACT[C/T]TACAGAGGCTAGGAG | 84669 |
rs557592766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60285878 | ACAGTGGCTCACGCC[G/T]GTAATCCCAGCACTT | 84669 |
rs557609719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223181 | ACAACATTTTCAGAA[A/T]AGCTGTCCTAAGTAA | 84669 |
rs557646529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60186136 | CACAAATGTTACATC[A/G]GTAACATTCTGGATA | 84669 |
rs557658197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60293445 | ACAAACAAATCATAG[C/T]TCAGTTCGTCCTGAA | 84669 |
rs557665049 | in-del | -/TTTT | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60366146 | CCACGCCGGGCTAAG[-/TTTT]TTTTCTTTTTTCTTT | 84669 |
rs557670352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60246406 | GTGTGTGTGTATATA[C/T]ATATATATTTTTTTT | 84669 |
rs557686928 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60271669 | AATTAAACCAAAATA[A/T]ACAAAATGAAGCTTT | 84669 |
rs557704122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318121 | TTTGTAAATGACAAA[A/G]TTGGTAGGGATGGCT | 84669 |
rs557721168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360433 | GGAGGCCAAGGTGGG[C/T]GGATCACCTGAAGTC | 84669 |
rs557726346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60342951 | GTCCAACCAGTCCCA[A/G]TGAGATGAACCAGGT | 84669 |
rs557734837 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60323655 | AACAAAACACTATTT[A/C]TTTTAAAGCAAAGAA | 84669 |
rs557743438 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60179019 | CCTTTTGTTTACAGG[A/C]TAATGGTGGGATCTG | 84669 |
rs557776063 | in-del | -/TGT | | | intron-variant | USP32 | GRCh38.p7 | 17:60337950 | CATTATCTAATAAAA[-/TGT]TGTGCTATGTACTAC | 84669 |
rs557782760 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60394483 | CCCCACTTGAAAGAC[A/G]GGACTAGAGTTGCAG | 84669 |
rs557795062 | in-del | -/TATAG | | | intron-variant | USP32 | GRCh38.p7 | 17:60383313 | TTTGAGGTGGATACA[-/TATAG]TATAACTCGATTCCT | 84669 |
rs557799458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415090 | TTATTTTCATGCTTG[A/G]GGAGGGTGGTATCCA | 84669 |
rs557803731 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60287118 | TCGCGCCACTGCACT[C/T]CAGCCTGGGCGACAC | 84669 |
rs557814221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60278856 | CAGATTTAAAATAGT[A/G]AAAGTCTGATTAAAA | 84669 |
rs557814336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60287603 | AATTGCGATTCTATA[A/C]CAGGACTTCAGAGGG | 84669 |
rs557818982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317527 | TCTAAAAAAAAAAAA[A/C]AAAAAGTTAAAATGG | 84669 |
rs557836070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423225 | GAGACAGAGTCTCAC[C/T]CTGTCACCTAGGCTG | 84669 |
rs557838383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60209309 | TTTAAGTTGTGCTAC[A/G]TGTATTTGTGGCCAG | 84669 |
rs557862919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60367744 | ACCTGGGAGGCAGAG[A/G]TTGCAGTGAACTGAC | 84669 |
rs557875276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286919 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACTTGAG | 84669 |
rs557887723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286207 | GAAAGAAGAACAGTA[C/G]AAATTAACACTTAGG | 84669 |
rs557895060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60303058 | TTATAAATATATTTA[A/G]TAACACCTGACAACT | 84669 |
rs557899396 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60385447 | GCTACTTTGGAGTCT[C/G]AGGCAAGAGAATCGC | 84669 |
rs557911975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60352622 | TTAAACAAAGAAGTA[A/G]CAATCAGGTTTACAT | 84669 |
rs557936374 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60352488 | AAATAAACCCTTATA[C/T]CTTATTTAAACTATT | 84669 |
rs557943167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401079 | GAGGATGGCTTGAAC[C/T]GGGGAGGTAGAGGTT | 84669 |
rs557944788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408184 | AAGAAGCAGGGGGGA[A/G]AAATCAGGTGACAGA | 84669 |
rs557951245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60349671 | TATATATACACATAT[A/G]TATATACACACATAT | 84669 |
rs557955795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216758 | ATTTGAGAAAGATGA[A/C]CATCATGTTATGGCA | 84669 |
rs557962596 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60180876 | TAATTACTATTATTA[C/T]TATTATTATTATTAT | 84669 |
rs557984020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60255399 | GCCTCCTGGGTGCAA[A/G]CGATTCTCCTGCCTC | 84669 |
rs557998504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326396 | GCTCACTGCAACCTC[C/T]GCCTCCTAGGTTCAA | 84669 |
rs558026905 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415865 | GTTTTTTTGAGATTG[A/T]GTCTCACTCTGTTGC | 84669 |
rs558047719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254816 | AGGCCTTTTATTTAT[C/T]TATTTTCTTTTAAAA | 84669 |
rs558077561 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60389701 | TTGCTTTAATTTTCC[C/T]CTAAAGCAAACTGGT | 84669 |
rs558078552 | in-del | -/TTA | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60318866 | TGAAAAATTGACCAC[-/TTA]TTTTTAAAATAAGTT | 84669 |
rs558080255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407729 | GGAGGTTACAGTGAG[A/C]CGAGATTAAGCCACT | 84669 |
rs558122412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60184827 | AAAAAAAAAAAAAAA[A/C]AACATATAAATATCT | 84669 |
rs558139064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422753 | CAATGATAGGGTACC[A/T]GAGATAGCAAGAGGC | 84669 |
rs558148971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400166 | AACGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 84669 |
rs558159946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60262259 | TGCAATGGTGTCATC[C/T]TGGCTCACTGCAACC | 84669 |
rs558160531 | in-del | -/CTCCCAAGAGTCCTTGGGAGTCTGAGGA | 0.0119091 | 0.0762411 | intron-variant | USP32 | GRCh38.p7 | 17:60312532 | CAGGCTCAAGTGATC[-/CTCCCAAGAGTCCTTGGGAGTCTGAGGA]CTCCCAAGAGTCCTT | 84669 |
rs558175891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268705 | AATAGAGATTTGAAT[G/T]TTTAGTTGAAAAATT | 84669 |
rs558183006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60273587 | CAGATGCTCAGATAC[A/G]TAACATCCACAATGT | 84669 |
rs558203970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236882 | CCTCTTTGACTTTGC[C/G]TGTTTTTGTGGTTCA | 84669 |
rs558205519 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60202136 | CATATGGATATCTAA[C/T]TGTCCCAGCACCACT | 84669 |
rs558220100 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60314207 | ATACAGTGGCATTGA[A/T]CTTGGCTCACTGCAA | 84669 |
rs558225700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261711 | AATGTAATTTGATAT[A/G]TGTGATAAATTATTA | 84669 |
rs558230723 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377229 | CTTTGGGAGGCCAAG[A/G]CAGGAGGATCTCTTG | 84669 |
rs558241008 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60214203 | CACCTCGGCCTCCCA[A/G]AGTGATGGGATTACA | 84669 |
rs558260372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223865 | AATTATATGTCCTCC[A/G]ACTGGAAGGGAAGAG | 84669 |
rs558271466 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418802 | AGAAATGCAAATCAA[A/G]ACCACAGTGAGATAC | 84669 |
rs558310541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266155 | GTATAATATATTTTA[C/G]TAGAAGTTGCCCTTG | 84669 |
rs558327170 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60221569 | GAGTGCAATGGTGTG[C/T]AGTCTTGGCTCACTG | 84669 |
rs558331410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60223135 | AAAAATACTAGTTTG[A/G]AAAAAAAAATTCATA | 84669 |
rs558335414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60355434 | CGATTGCCGGAATGG[C/T]AAAGACCTCTGAAAA | 84669 |
rs558344976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381363 | GAAGGATTGCATGAG[C/T]GCAGGAAGTAGAGGC | 84669 |
rs558353571 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60286271 | ATTCATGATTATCTG[A/G]AACCTCAGAATATGG | 84669 |
rs558357487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60323437 | ACAGAAAGTAGATTA[G/T]TATATTAGTTGGCCA | 84669 |
rs558365155 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60198810 | ATTAAGGCTCTTTCT[C/T]TCTCCAGAAAATATG | 84669 |
rs558370790 | snp | C/T | 3.30464e-05 | 0.00406474 | synonymous-codon | USP32 | GRCh38.p7 | 17:60185613 | GGGCTCGGCTTGCGC[C/T]CGCCGACTCTGCTCC | 84669 |
rs558379255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60389417 | GAGTGGTGGCATGCG[A/C]CTGTAGTCCCAGCTA | 84669 |
rs558384820 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60254997 | TATTTCCCACGTCAC[A/G]ATTTTGACAAACTTC | 84669 |
rs558388438 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60342101 | TTTGGTGTAGATGTC[C/T]TTTTTGTTGATGATG | 84669 |
rs558393837 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410767 | TCACAAGAGTCAAAA[A/G]CACATAACATAGGTT | 84669 |
rs558398724 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60333690 | AGGGAGGGAAAGAAA[A/G]GAGAGGAGAGGAGAG | 84669 |
rs558408974 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60230335 | ATTCCTGTAATAATG[C/T]TTCTCATTCTGAAGA | 84669 |
rs558411322 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60237124 | TACTCTATCTATCTA[-/C]TCTATCTATCTATCT | 84669 |
rs558414337 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60396354 | AGTGCTGGGATTATA[C/G]GTGTGAGCCACCACG | 84669 |
rs558449430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60244865 | TCGAACTCCTGGCTT[C/T]AAGAGATCCGCCTGC | 84669 |
rs558494321 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419510 | GGGAGGCTGAGGTGG[A/T]TCACGAGGTCAGGAG | 84669 |
rs558494652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234526 | AGGTCAGGAGATTGA[A/G]ACCATCCTGGCTAAC | 84669 |
rs558524439 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60379403 | AACATCTACTACATT[C/T]CAGATTTAGGGACTC | 84669 |
rs558531499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60350896 | CCAAAAGCTATTGAA[A/T]TTTTTTTTTTAACTC | 84669 |
rs558532326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60248959 | TCTGAACCCCTGTGT[A/G]TTTTGTTTTGTTTTA | 84669 |
rs558558298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60387950 | TATAGCTTCTGCACC[A/G]TCGTAAAGTTAAATT | 84669 |
rs558562294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288944 | GTAAAGCAGTACACT[A/G]CCAATAAGCCAGATT | 84669 |
rs558565121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258019 | CTAAGAGTCTTCCTC[C/T]GGCACAAATGGAAGA | 84669 |
rs558592057 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60247969 | GATTACAGGCGTGAG[C/T]CACCACGCCTGGCCT | 84669 |
rs558593936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257167 | AAAAGGAGATGGGAG[G/T]CCAGCTCAAGTCTGT | 84669 |
rs558608803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407475 | TCTAAACTAGGTCTA[A/G]AGTAAAGTACACGCT | 84669 |
rs558631238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60380760 | TACCCTATTCATACC[C/T]ACTACTCATTTGCTA | 84669 |
rs558645565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60322436 | GGATTTCATTTTGGC[C/T]CTCTGTATTAGTAAA | 84669 |
rs558673060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221382 | CAACATCAAAATTAC[A/G]TTAGTCTGTTTTATA | 84669 |
rs558682227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330810 | TAACTTCATATCATA[A/G]GGAAAAGACAGAGTT | 84669 |
rs558696633 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60201803 | AGCTGGGACTACATG[-/T]GCCCACCATCACGCC | 84669 |
rs558707172 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309234 | ATATTTGCAAAATAC[C/G]CATCTTACAAGGGAT | 84669 |
rs558707371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256628 | CACATCCCAAAGACA[C/T]ACACGTTAGGTTAAC | 84669 |
rs558723824 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60370643 | ATGGTGGTGCCCACC[C/T]AACCACTCAGGAGGA | 84669 |
rs558734476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60220801 | GGAGCCCGCCACCAC[A/G]CCTGGCTAATTTTGT | 84669 |
rs558735442 | in-del | -/ATGTTATTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60243562 | CTGTGCTCTAGTAAA[-/ATGTTATTT]ATGTACACTGAAATG | 84669 |
rs558744981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227667 | ATACTCCTGCCTGGG[C/T]CTCCCAAAGGGCTAG | 84669 |
rs558762526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60379536 | TTTTCAAATTCTCAA[A/G]CTGACACAAATACAT | 84669 |
rs558773609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60181112 | TGGGCTCAAGTGATC[C/T]TCCTGCCTCAGCCTT | 84669 |
rs558778689 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60204196 | AAAAACAAAACAAAA[A/C]AAAAAAACCAACCCC | 84669 |
rs558789665 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60192479 | TCGCTCTTGTTGCCC[A/G]GCTGGAGTGCAGTGG | 84669 |
rs558792149 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60338591 | AAAAATTAGCTGGGC[A/G]TGGTGACACGCACCT | 84669 |
rs558792784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212318 | TGTACCTACACAAAC[C/T]TAGGCTATGTATGGT | 84669 |
rs558797576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378647 | GTACTACAACATGGA[G/T]AAACCTTGAAAACAT | 84669 |
rs558813143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409323 | ACAGCATTCCAGCCT[A/G]TGCAACAGAGCGAGA | 84669 |
rs558846338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190094 | TCTTGCAGTAGTTGA[G/T]TTCTCCTTCTGAGAA | 84669 |
rs558847243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234207 | CAAGCTCCGCCTCCC[A/G]GGTTCAAGCCTTTCT | 84669 |
rs558853086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417090 | ACCCAGTTAATTTTT[A/T]TATTTTTAGTAGAGA | 84669 |
rs558864911 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60264232 | AACCATTTAAAAAAA[A/T]TTTTTAGGCCAGCAC | 84669 |
rs558866163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306453 | GAGCTGCCTGGCCAA[C/T]GTGGTAAAACCTTGT | 84669 |
rs558866206 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60342725 | CGTGGGCATGGGACC[C/T]GCTGAGTCAGGCACG | 84669 |
rs558900761 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60246570 | ACCCAGCAGTGGGAT[C/T]GCTGGATAATATGGT | 84669 |
rs558905702 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306564 | AATCACTTGAACCCG[A/G]AAGGCAGAGGTTACA | 84669 |
rs558907969 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60273170 | TAGAGATGGAGTTTC[A/G]CCGTATCACCCAGGC | 84669 |
rs558929930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60337983 | AGATTCAGGCTTTAA[C/T]GCTTGAAAGAGAGTT | 84669 |
rs558936292 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60346762 | TTCTTCCAGATGAAG[A/T]TAATTACATTAAATT | 84669 |
rs558940949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60263130 | CGTTTTTTCTTTTTT[C/T]AGAGATAGAGTCTCG | 84669 |
rs558944482 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60276105 | ATATAACGGCTGGGC[A/G]TGGTGGCTCACACCT | 84669 |
rs559000361 | snp | A/T | 0.00050584 | 0.0158954 | intron-variant | USP32 | GRCh38.p7 | 17:60211973 | TTGAGAGAAGAAAAA[A/T]AAAGAATACATTTAA | 84669 |
rs559001355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410105 | CACAAGATTTGTAAT[A/C]TCCCCAGTTGCTCCT | 84669 |
rs559001641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60269865 | ATAAAAATTAAAAAC[A/C]AAAAAAAGGTCAGAA | 84669 |
rs559025259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196818 | TGACAGAGCGAGACT[C/T]TGTGTCAAAAAAATA | 84669 |
rs559036796 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60218512 | TTGGTCAGGGTTTAG[A/C]GGTAGTTCTTGCATA | 84669 |
rs559039560 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60314968 | CCTAGGATTATATAT[C/T]CAACAACAAAATGAC | 84669 |
rs559058812 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418027 | GCAATGGCACGATCT[C/T]GGCTCACCACAACCT | 84669 |
rs559062003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211322 | GAAATTTAGGTGATA[C/T]TGGGTTTATATCAAA | 84669 |
rs559068426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320639 | AATTGATGTTTTTTT[A/C]ATCAACATTATAATG | 84669 |
rs559070273 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60304787 | AATTACGTGACCTTA[-/G]GTAATCTAGTGTTTA | 84669 |
rs559078856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363181 | TTTTTGAGGCCAGGC[A/G]CGGTGGCTCACACCT | 84669 |
rs559144614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312197 | TGGGAAATACTATCT[C/T]AGGACAGAAGGCGGA | 84669 |
rs559148745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263883 | AGAAAAAAAACTGAC[A/G]TTCTTTATTTATTCT | 84669 |
rs559188681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60219044 | GGAACTACTTTATAT[A/G]TCATTTTGATAGGCT | 84669 |
rs559191839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60368961 | GGCAGAAAAGGAGTT[A/C]GTACACATACACGAA | 84669 |
rs559200273 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60271060 | CCAGGCACTAGCTAC[G/T]AATGCACCTTACTGG | 84669 |
rs559211314 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60367028 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 84669 |
rs559222216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60219241 | ATAGTATAAGAGGAA[C/T]TGCTTTTTACAAATT | 84669 |
rs559226615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60287065 | TGAGGCAGAAGAATC[A/G]CTTGAACCTGGGAGG | 84669 |
rs559229614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60328755 | TCCAAGCTTCCAGAC[A/G]CCATCACACTCCCCG | 84669 |
rs559257264 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178482 | CTTGAAGTATCCTAA[A/G]TGTAAGATGCCTCCA | 84669 |
rs559274681 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60304660 | GATGGGAGAAAGGAA[C/T]TGGAAGTATACTGTT | 84669 |
rs559292120 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60383798 | GGTAAATTACTACAA[C/T]TGAGGTTGGAGTTTT | 84669 |
rs559296445 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60337131 | CAAATACAAATCACT[A/G]TTCTGTGATACTCTC | 84669 |
rs559313318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312512 | CTCATCGCAGCCTTG[A/G]CCTCCCAGGCTCAAG | 84669 |
rs559318411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60319331 | TTCAGATAATAAATA[C/T]GAGTATAATAAACAC | 84669 |
rs559420647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408616 | CTCCTGACCTCAAAT[A/G]ATCTGCCCACCTCAC | 84669 |
rs559428104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256753 | GGCTATGTAAGATCT[A/G]CCAATCTCCCAAATC | 84669 |
rs559442178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60264007 | CAAATGTGTCTCATA[C/T]AGGTAATTTATTTTC | 84669 |
rs559512373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225394 | GCCAGGAGGCAGAGG[C/T]TGCAGTAAGCCGTGA | 84669 |
rs559514778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60250517 | ATGTATGTCCTTACA[A/G]TATCTGGTTTCTACA | 84669 |
rs559521428 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60343756 | ACTAGAGAAGGCCAG[G/T]CATGGTGGCTCACGC | 84669 |
rs559529137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414726 | GAGCCACCACGCCCA[G/T]CCAGTTATTGTTTTA | 84669 |
rs559530411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60270313 | CAAGTACTTCCGAAG[C/T]ACTCTAGAAATTTGA | 84669 |
rs559559048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60336296 | AAACTTGACAACTAA[A/G]GACCATCAAGATAAT | 84669 |
rs559565832 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60199311 | TAAGTGATTTTAATC[-/T]TTTTTTTTTGTTTTT | 84669 |
rs559574664 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60329659 | CTTTTCTCCCTTCCT[C/T]AACTCTTAAAAGCAA | 84669 |
rs559591630 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | USP32 | GRCh38.p7 | 17:60401235 | CCAAGGTGGGCGTGG[G/T]GGTGGGCGCCTGTAG | 84669 |
rs559606892 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60194206 | GCAACACCATACCTG[A/G]CTAATTTTTACATTT | 84669 |
rs559618577 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394069 | GCCCTTTCCAGTTCA[C/T]TGTGAGGTGGTTAAT | 84669 |
rs559631649 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP32 | GRCh38.p7 | 17:60387203 | TAGTATAAATCTAAC[A/G]AAATTTTAAGATTAA | 84669 |
rs559633695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378252 | GACAATACTATGTCA[C/T]ACCCATTAGGATGGT | 84669 |
rs559634473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268233 | GTTCATCAGCAAAAA[A/C]AGAAATTAAAACAAA | 84669 |
rs559650781 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60278050 | TAGCTGGGAATATAC[A/G]CATGTGCTACCACAT | 84669 |
rs559661589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401844 | GATAATATTAACAAA[C/T]AAATCAATTCATGCA | 84669 |
rs559680566 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404088 | GAAAAAGAAATATGC[A/G]CACACACACATATTT | 84669 |
rs559684805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60282807 | ACTCTGGAGGCAATC[A/C]AATGTTTAAATCAAG | 84669 |
rs559693865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60344507 | CAGGCTGGAGTGCAG[C/T]GGTGCAATCATAGCT | 84669 |
rs559707623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60309783 | GGGCACAGTGGCACA[C/T]ACCTGTAATCCCAGC | 84669 |
rs559708305 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60350495 | GGTTTCACCACGTTG[A/G]CCAGGCTGGTCTCAA | 84669 |
rs559709060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232763 | GGTTGGGCAGGTTGG[G/T]GCTGAACTCCCAGCC | 84669 |
rs559716964 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407928 | CATGGTGAAACCTCG[C/T]CTCTACTAAAAATAT | 84669 |
rs559726657 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60186882 | CCGGGATCCTTCTGT[C/T]TGTCCCTCTAATGTA | 84669 |
rs559761287 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60246628 | CTCCATACTGTTTTC[C/T]ATATTGACTGTACTA | 84669 |
rs559783046 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60239572 | CTTCTCTGATTCATT[C/G]TTCTGCCTGCTCATA | 84669 |
rs559789348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194682 | ACCCCATATGTAAAC[C/T]CTCTCCAAATGTCAT | 84669 |
rs559802006 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60376179 | GCTTCCCAAGGAGCT[C/G]AGATTACAAATGCGA | 84669 |
rs559817336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353014 | AATTTGAATATATTA[C/T]ATTGTATTTACATTT | 84669 |
rs559832144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302560 | TTTATCGGGCTGTAA[C/T]CCCAGGTAAGTAGAG | 84669 |
rs559839987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60352249 | CTTAAAAGGTAACAG[C/G]TGGCAAATATCCTTT | 84669 |
rs559849592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404773 | TGAGAAACAACCTTC[C/T]CATCTTTCCTGTATG | 84669 |
rs559852528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60398919 | CCAGGAATTTGAGGC[C/T]GCAGTGAGCTATGAT | 84669 |
rs559884504 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411859 | TCTATTGCATGCATA[C/T]ACCACATTTTTTTAT | 84669 |
rs559906890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60369274 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 84669 |
rs559920971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60342710 | CAGTGAGCAAGGCTC[C/T]GTGGGCATGGGACCC | 84669 |
rs559926483 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60209886 | ATCCTGTTCTATAAC[A/G]TTTTACATTTTTATA | 84669 |
rs559928587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60368012 | TTACATGCAAATACT[A/T]CACCATTTTATATAA | 84669 |
rs559954886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60210414 | CCTCCCAGGTTCAAG[C/T]GTTTCTCGTGCCTCA | 84669 |
rs559965667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377228 | ACTTTGGGAGGCCAA[A/G]GCAGGAGGATCTCTT | 84669 |
rs559984500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60191227 | ACCAACATGGTGAAA[C/T]CCTGTCTCTACTAAA | 84669 |
rs559987865 | in-del | -/GCTACTCAGGAG | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60184201 | GCGCCTGTAGTCCTA[-/GCTACTCAGGAG]GCTGAGGCAGGAGAA | 84669 |
rs559999734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318392 | CTAATCTAATTCCAT[C/T]TAGAGAACAGCATGG | 84669 |
rs560025590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60372394 | GACTACTACACACCT[A/G]GGCTATATGGGATGG | 84669 |
rs560041372 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60238687 | TGGGCACCTATAATC[C/T]CAGCTACTTGGGAGG | 84669 |
rs560044126 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60397580 | TTGCCCAGGCTGGTC[C/T]CAAACTCCTGGACTC | 84669 |
rs560063571 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60362592 | AGAGTCTTAAACATA[C/T]CATGGAGAGAATGTC | 84669 |
rs560064942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306861 | AATCAAAATACAAAA[A/G]TCAATACAATTTATA | 84669 |
rs560096211 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419810 | CCTGCAACTCAAGGT[C/T]AAAAAAAATTATTAT | 84669 |
rs560118606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60365076 | CATGTTATTTCAAAA[A/T]GGGAAAGTTTTTTTT | 84669 |
rs560137771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227912 | CTGTATGGCATTACA[A/T]GAGAAAAATGGTGAC | 84669 |
rs560158411 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60381024 | TTTGCATAAATGTCA[G/T]GAGACAAAATTTACT | 84669 |
rs560170692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60340678 | ATTTACATTTAAGGT[G/T]AATATTGTTACATGT | 84669 |
rs560188531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60398288 | GTAGTCTCAGCTACT[C/G]AGGAACCTGAGGTGG | 84669 |
rs560198637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190471 | TTTTCTGGTTGTTTT[G/T]AAATTGTCTAAAACA | 84669 |
rs560201446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235525 | GGAAATACAGGCAAA[C/T]AGGAATCAAATGATT | 84669 |
rs560209617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348660 | GTGCCTATAGCTACT[A/C]AGGAGGCTGAGATGG | 84669 |
rs560230783 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395378 | AGTTAAATTAAGCAT[A/G]TTATTGTAGCCAGTG | 84669 |
rs560237178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60388064 | CATTTCCTTAGTGCC[C/T]AATTCATACCCAGCC | 84669 |
rs560244267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60298160 | ACCCCAAAGTAAACA[C/T]GGGACACATATAACA | 84669 |
rs560245954 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60348089 | ATAGCGCCACTGCAC[C/T]CCAGCCTGGGCAACA | 84669 |
rs560248034 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60186180 | TATGACCATAGCTTT[A/T]CTTGAAAAATTTTTG | 84669 |
rs560248531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221120 | CACTACAAGCCAGGT[A/G]CAGTGGCTCATGCCT | 84669 |
rs560249664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60226967 | GAGAATCACTTGAAC[C/G]CGGGAGGTTGCAGTA | 84669 |
rs560278807 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233082 | GTCATAAAGCAAGTG[C/T]AAGGGACAAGAGTCC | 84669 |
rs560308174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306432 | CATTTGAGGTCAGGA[A/G]TTCGAGAGCTGCCTG | 84669 |
rs560311277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60272965 | CAAATGCCGGGAAAT[A/T]TGTTTTGTTTTGTTG | 84669 |
rs560330287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60346045 | TACACTTCTTTTTTG[A/G]TTAAATAAAACTCTA | 84669 |
rs560369931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355241 | AGGAACAACTCATCA[A/G]TGATGACAGGTCAGA | 84669 |
rs560400828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315164 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGAATGC | 84669 |
rs560419068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356496 | CACACCCGAGTAGTA[C/T]AGAACCCCTCCGCCA | 84669 |
rs560419242 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182645 | GTGCATGCCTGTAGT[C/T]CCAGCTACTCAGGAG | 84669 |
rs560517193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298700 | TTTATATTTCTGCTG[G/T]TGAAGAAATGCTAAT | 84669 |
rs560557294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281565 | ATGCTGTATACCAGA[C/T]GCAGGCTGAGTCCTT | 84669 |
rs560558192 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60220412 | TATAAAAATTTACTA[C/T]GTTCTACTTGCGTAA | 84669 |
rs560575216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190433 | TCAATATATTAGGTG[C/T]CATAGAGGATGCCAA | 84669 |
rs560584471 | snp | C/T | 8.23635e-05 | 0.00641677 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181486 | AGCTACCTCATGGTC[C/T]TGAGGAGTGACCAAC | 84669 |
rs560615701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196979 | TGAGGCCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 84669 |
rs560642453 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60400360 | ACACAGGGAGACCAA[C/T]TAGGGGGCGACTGCA | 84669 |
rs560644959 | in-del | -/AAAT | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410671 | AAACACTGTCTCAAA[-/AAAT]AAATAAAGAAAGAAA | 84669 |
rs560658269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305663 | ATGGTAACAAATTCA[A/G]TTTATAAACACTGAG | 84669 |
rs560666588 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60328594 | AGGCTAAAAGAGCTA[C/T]AACATAAACAGAGCT | 84669 |
rs560682762 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404649 | TGGTTTATAGGGAAA[G/T]TGTAGAAGAGTGCAC | 84669 |
rs560685278 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410992 | ACCAGCCTGGACAAC[A/C]TAATGAGACCTTCAC | 84669 |
rs560686627 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60300564 | AAAACATTAAAAAAA[G/T]TAAACCTTTTACAAA | 84669 |
rs560696813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60180488 | ATTTCAACAAATGTT[C/T]CCCAGTTCTGTTGAT | 84669 |
rs560698293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60395732 | GTTATCCATATAAAG[A/G]TTTAAAGCACAGGAG | 84669 |
rs560703891 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395874 | CAAAGAACCTTAGGT[A/G]AGCTAGAGAGAGGGA | 84669 |
rs560714813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60338144 | GCCTGGGCAACATGG[C/T]GAAACTGCATCTCTA | 84669 |
rs560720257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305834 | TTTGCAAGTACTTGT[A/G]AAATGTAACAGATTT | 84669 |
rs560750286 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60360355 | TACAAATACAAAAAA[-/T]TTTTTGTATTTGTAT | 84669 |
rs560758622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418287 | TAGTAGAGACAGCAT[C/T]TCACCATCTTGGCCA | 84669 |
rs560758901 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264728 | CAGCCGGCATGGTGG[C/T]ACACACCTGCAGTCC | 84669 |
rs560762192 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403160 | GGGTCTACAGGCGCG[C/T]GCCACCACGCCCAGC | 84669 |
rs560794130 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373959 | GGAGGCCGAGGTGGG[C/T]GTATCACCTGAGGTC | 84669 |
rs560797272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265571 | GCAAGATTTGTTTTG[C/T]TTTTCTTGTAGAGAT | 84669 |
rs560809932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197966 | TGAATTCATACTCTC[C/T]ACTTTTGCAACACAG | 84669 |
rs560821528 | snp | C/T | 1.65034e-05 | 0.00287253 | missense | USP32 | GRCh38.p7 | 17:60205527 | CATTAACCATTCCAT[C/T]TGTGAAGTTCTTCTC | 84669 |
rs560826111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60397161 | AATGCATAGAATAAT[A/G]TGGACTCCAACTTTG | 84669 |
rs560830689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60188913 | ATAGCCCTTCACTTC[C/T]ATGGTATCCTAAGTG | 84669 |
rs560832131 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60390632 | ATCTTACTGTCAGGT[A/G]ATGGTCAACTGAACT | 84669 |
rs560846793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196651 | CCGACATGGTGAAAC[C/T]CTGTCTGTACTAAAA | 84669 |
rs560869793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271952 | AAGTAGCTAGGACTA[C/T]ATGTGTACGCCACCA | 84669 |
rs560888967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60314558 | AAAGAGCTAGAACTG[A/G]GGGTGGGGGGAGGAA | 84669 |
rs560902125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387964 | CATCGTAAAGTTAAA[C/T]TGTAAGTCGGGGATT | 84669 |
rs560936535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356418 | GGCTGACCTTAAACC[G/T]CCACACAAGCAGGAA | 84669 |
rs560940351 | in-del | -/AT | 6.76888e-05 | 0.0058172 | intron-variant | USP32 | GRCh38.p7 | 17:60211171 | TCATAAATCACAATC[-/AT]GTGGGCGCAAAAATG | 84669 |
rs560954122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190275 | AACTTCCCAGGCTGC[C/T]GAACAGTAAGCTAAA | 84669 |
rs560963027 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60323318 | TTCAACAATAAAAAG[C/G]AATAAAGGACTGATA | 84669 |
rs560966738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60372320 | TGACAGGAATGCATC[A/G]TTAGGTGATTTCATC | 84669 |
rs560971481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347416 | AGGAGTGCAGTGGCA[C/T]GATTTCTGCTCACTG | 84669 |
rs560980435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60271225 | ATTTGTTTTTCCCCA[C/T]TCCATTAAACCTGCA | 84669 |
rs561002971 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | USP32 | GRCh38.p7 | 17:60380860 | TAATAAGAATTAGAA[A/C]TTTGTGCTTGTCCTT | 84669 |
rs561031798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60213320 | TGAATTCACTTGTTT[C/T]TTATCTACCATTCCC | 84669 |
rs561036996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403989 | AGGCCGCAGTGAGCC[A/G]CGATCACACCACTGC | 84669 |
rs561038283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387492 | CCGTAGCACTTTCTC[C/G]TATAGCACTGCAGCA | 84669 |
rs561038326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60395570 | TCTGCTTGTCATGCT[A/G]AAAGGAATTCTATTA | 84669 |
rs561071450 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60322605 | AAGATTAGAAAACAC[A/G]AAAATTAACTGACTC | 84669 |
rs561074598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60394898 | ATAGGCGCACACCAT[C/T]CCGCCCGGCTAATTT | 84669 |
rs561082298 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408454 | ACGATCTTGGCTCAC[C/T]GCAAGCTCTGCCTCC | 84669 |
rs561101311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204854 | GCATGGCTCACTGCA[C/G]CTTTGACCTCCTAGT | 84669 |
rs561123556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249497 | TTTTATCCCCAAGCT[G/T]GTGATGTCAGTTTTC | 84669 |
rs561127387 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60187151 | AATTGGCACAGCTCA[A/G]GACATTCAGTTTAGA | 84669 |
rs561145867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401598 | GTAGACCTCTGGGGG[A/C]TGGGTGCAGTGGCTC | 84669 |
rs561145922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60313506 | GGCCCCTTGAAATTC[C/T]GAATAAATAACAACA | 84669 |
rs561146485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212791 | ACAGTCTGGCTTTGT[A/C]CCCCCAGGTTGGAGT | 84669 |
rs561153727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60248345 | AATGATATGTCTAGG[C/T]GTGATTCTTTCTGTG | 84669 |
rs561159226 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60280991 | CAGAAGCCAGCAGCA[A/G]TTCAGTTGTCTGTTG | 84669 |
rs561187728 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60345993 | TCTCAAAAAAATAAA[A/T]AAATAAAAAGAAAAA | 84669 |
rs561188788 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227852 | GTAGCCAAAAAATTT[G/T]TTTAAATTTTAAGTA | 84669 |
rs561209848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60220269 | AGTAATGTGTAAGTA[C/T]ACTACTCTCATAAAA | 84669 |
rs561216766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60371562 | CAACAGAGCAAGATT[C/G]TGTCTCAAAAAAAAA | 84669 |
rs561219262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362064 | ATGGATGGTGGCTCC[A/G]TATCTTTACTTCACA | 84669 |
rs561219510 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60247655 | TGTAAATGTGGGGGG[G/T]TTTGCTTGTTTGTTT | 84669 |
rs561220489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288402 | CCACGATGGTGCCAC[C/T]GCACTCCAGCCTGGG | 84669 |
rs561221992 | snp | C/T | 0.000103087 | 0.00717866 | intron-variant | USP32 | GRCh38.p7 | 17:60219598 | TTTTTTAAGGAAATG[C/T]ATGGTATTCTTGCTG | 84669 |
rs561254460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60361432 | ATAACATTAGTAATA[C/T]ACAGGTATTCACTTA | 84669 |
rs561282987 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60311244 | AGTGATCACATGTAC[C/T]CCCCAAAAAATGTAT | 84669 |
rs561291388 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60338029 | ACAATGTTGGCTAAA[A/G]TTGTTGGACGCAGGC | 84669 |
rs561303112 | snp | A/G | 5.00238e-05 | 0.00500094 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181338 | CCGAAATTGCATATA[A/G]ATTATAAATAGGCTT | 84669 |
rs561358981 | in-del | -/CACCT | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60327504 | CCGCCCACCCCACCC[-/CACCT]CACCTCAGGAGCCAG | 84669 |
rs561359252 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60203776 | GAGACGGGGTTTCAC[C/T]ATCTTGGCCAGGCTG | 84669 |
rs561361674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231276 | AATTAACAGTTATGT[A/C]AATTTCATATTTCAC | 84669 |
rs561373669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267682 | TCCACCACCACGCCC[A/G]GCTAACTTTTGTATT | 84669 |
rs561392382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384566 | GGAGGCCGAGGCGGG[C/T]GGATCACCTGAGGTC | 84669 |
rs561392946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353314 | AAACCTTGCTGGAAC[C/T]CAACGTTATTTCCAA | 84669 |
rs561428739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280200 | CTCCTGGGTTCAAGC[G/T]ATTCTCCTGCCTCAG | 84669 |
rs561429123 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense | USP32 | GRCh38.p7 | 17:60392378 | GGACGCATCTCCGCA[C/T]GTAACGCATCGTCCC | 84669 |
rs561435346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296361 | AATATAATATGACTG[A/G]TGCCCTTATAAGAAG | 84669 |
rs561440791 | snp | C/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60287909 | ACGAGGTCAGGAAAT[C/T]GAGACCATCCTGGCT | 84669 |
rs561453969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312353 | TCAACAGAACCAAAT[G/T]AATGTTTTCAAATTT | 84669 |
rs561462150 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60248736 | CTTTAAATACAGCTT[A/C]GTTTAGCTCTTTGAA | 84669 |
rs561462516 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60233738 | CAACTTACATTTCCC[A/C]CACCTTATTAATAAG | 84669 |
rs561465913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60391780 | CCCTTCCGCCTCAGG[A/C]GCCCCACGCCCTCAA | 84669 |
rs561491788 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60272316 | AGTAGGAGTCCCTAT[A/G]TGATAGCAATAGCAA | 84669 |
rs561491957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60187718 | AAACATATTTGTGGA[A/C]TGTACTGACAATAAT | 84669 |
rs561494830 | snp | G/T | | | synonymous-codon | USP32 | GRCh38.p7 | 17:60301621 | TTTCTCTTCATCTTT[G/T]CCTCTTGTAAGGAGG | 84669 |
rs561498890 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402631 | TTACTTTGCTTACAT[G/T]AGTATACCTGTGCTA | 84669 |
rs561519413 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60304080 | AGAGAACAAGCAGAA[C/T]AGATCACACCTATAA | 84669 |
rs561534780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237136 | TCTATCTATCTATCT[A/G]TCTATCTATCTATCT | 84669 |
rs561545491 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60222880 | AGAGACGGGGTTTCA[A/C]CATGTTGGCCAGGCT | 84669 |
rs561561010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60304483 | TACCTCCATAAAGAA[A/G]TAAGAATACTGGAAA | 84669 |
rs561565777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354101 | TAAGCTTTTTTCTTG[A/G]AGTTCAATACTTTAT | 84669 |
rs561578633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60350172 | CTCCCACTGCCACAC[A/G]TGGATAATTTTTTGA | 84669 |
rs561606012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417236 | TTCTTTCTTTCTTTC[G/T]TTTTATTTTAACTGT | 84669 |
rs561618317 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60216302 | GTGGCAAAAAAAAAA[A/C]AAAACATCATTAAAC | 84669 |
rs561619422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358893 | GATTGAGAATCTCTG[C/G]CTTAGGCCAAAAAGA | 84669 |
rs561634960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60284436 | CATATTGACCAGGCT[A/G]GTCTCGAACTCCTAA | 84669 |
rs561646253 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60280372 | AAAGTGGTGGGATTA[C/G]AGGCTCGGGCTACTG | 84669 |
rs561653992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358208 | TTCTGTAAGCCACCA[C/T]CCTATGAACCTAATC | 84669 |
rs561654667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326565 | TGGCCTCCCAAAGTG[A/C]TGGGATTAAAGGCAT | 84669 |
rs561675526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223276 | CACAGAAATGTACTA[C/T]ACAAAGAGATGTCCA | 84669 |
rs561678905 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177286 | ACAGATAAACAGGTA[C/T]ACCCCATATACAATT | 84669 |
rs561710399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60207259 | AACGAGATGATTGAA[C/T]AATTTTTCAACTACA | 84669 |
rs561714312 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60219495 | TTAATTACTGAGTCT[A/G]TAGGAAAGCTGATGG | 84669 |
rs561725567 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60252306 | TTACATTAAAATAGG[A/G]CATGCTGTTCCTCAG | 84669 |
rs561744588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60334271 | AAATGAGGCCATGTA[C/T]GATCTGTGTTTGTAT | 84669 |
rs561750876 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178568 | TCCCACAAGGCTCTG[C/G]GTGGAAGGCACACAG | 84669 |
rs561814526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60285371 | TCATGCCAGAACTTA[C/G]CAGTCAGAACTTTTA | 84669 |
rs561821681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60206694 | TATAATATTGGATTT[C/G]TTTCTAGCTATATCT | 84669 |
rs561834236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406395 | TGTTGCTCAAGCTGG[A/T]CTCAAACTCCTGGCC | 84669 |
rs561849657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60283244 | TCATGGTGTGGTCAC[A/G]GTATATTGACCAGTG | 84669 |
rs561887711 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60285434 | TGGTGTGTAATCTGT[A/C]GTCAAGTTATATGTC | 84669 |
rs561891508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325057 | TAGCTACAGGTGTTA[G/T]GAAAACTAAGCATAG | 84669 |
rs561891762 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60184152 | AAATAAATAAATAAA[A/T]AACACACAAAAAATT | 84669 |
rs561919968 | in-del | -/TA | | | intron-variant | USP32 | GRCh38.p7 | 17:60361864 | AGAGAAAGATACATG[-/TA]TATATATATATATGC | 84669 |
rs561921569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60252530 | CCTAAATTGGAATCT[A/G]AATTAGCAACAGTTT | 84669 |
rs561928820 | in-del | -/A | 0.0554779 | 0.157039 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413047 | AAACATTGCTACAGG[-/A]AAAAAAAAAGTGAAA | 84669 |
rs561931289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244641 | TTGTTTATTTTACTT[A/T]ATGTTTTTGAGATGT | 84669 |
rs561941962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60291502 | AGCACTAGGTCCTTA[C/T]ATTTTAGCTAAAGTG | 84669 |
rs561991198 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60253539 | GGGAGGCTGAGGCGG[C/G]CAGATCACTTGAGGT | 84669 |
rs562004727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60299737 | AGGGCAGCAGCTTAG[C/T]CTGTTGAGGCTGCTG | 84669 |
rs562022063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60374193 | TGTCTCCAAAAAAAA[A/G]AGAAAAAAGACATAA | 84669 |
rs562035536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412809 | TTCATTGACATTCAT[C/T]CAGTTCTCTCCTGCT | 84669 |
rs562048385 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60308724 | CTTGAGGTCAGGAGT[C/T]CAAGACCAGCCTGGC | 84669 |
rs562049446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289853 | TAGACATGCTAAAGA[A/G]TACGAATAATTAGTT | 84669 |
rs562050579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405742 | CATTCCTGCCTGGGC[A/G]ACAGAGTGAGATCCT | 84669 |
rs562050638 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60227517 | TCAGGTTATCTGCCC[A/G]CCTGGGCCTCCCAAA | 84669 |
rs562058930 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60337059 | AGCCCTTAATGCTGG[C/T]AAGTCCAACATAAAG | 84669 |
rs562064658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312210 | CTCAGGACAGAAGGC[A/G]GAAACCAGAGTTTGA | 84669 |
rs562072948 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60308197 | GGGATACAGAAAACC[C/T]TTGCGATAATGCAGA | 84669 |
rs562093588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221697 | TTTTATTAGACACGG[C/G]GTTTCACTATGTTGG | 84669 |
rs562094444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60391701 | CCAAACGGCCCTAAT[A/T]CCCAAACGCTGCTTC | 84669 |
rs562111918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259929 | TTGTGACTAGAAATA[C/T]GCTGTAGGAACTTAA | 84669 |
rs562179113 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP32 | GRCh38.p7 | 17:60266493 | TTGTTTCTTGTTCTT[C/T]TTTTTGTTTGTTGGA | 84669 |
rs562237398 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60390738 | TAATCTAATTACCAT[G/T]TTATATCCTTAGCTA | 84669 |
rs562237438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60399821 | GAATGAGGCAAGAGC[A/G]CATCTGCCAGCTCTA | 84669 |
rs562257078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315386 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 84669 |
rs562280156 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60355360 | CAAAATGCAAGGACA[C/T]ATGACTTTTGTATTT | 84669 |
rs562314843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60381660 | ATTTGGTCCCTGTCT[A/G]AACACTGTGTACCCT | 84669 |
rs562317771 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60320665 | TAATGAAAAACAACA[C/T]CGAATGAGTGATGAG | 84669 |
rs562362877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229593 | ATGGAGCAAGACAGA[C/T]AGCAAAACCATTTTG | 84669 |
rs562401964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390615 | ATACATCTCAATTCT[G/T]TATCTTACTGTCAGG | 84669 |
rs562438699 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60283711 | GGTGGATCATGGCAG[A/G]GAAAGATGAATTCAC | 84669 |
rs562451143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60291451 | AATAATAAAGCACAA[A/G]ATAGAAAAAGCTGAG | 84669 |
rs562481833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60341478 | TTGAAAATTCTTTAG[C/G]AATGTTGAATATTGG | 84669 |
rs562504163 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60185827 | AGCACTTTAGGAGGC[C/T]GAGGTGGGGTAATTG | 84669 |
rs562520692 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60287856 | TGGTGGCTCACGCCT[A/G]TAATTCCAGCACTTC | 84669 |
rs562527877 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60340758 | TGATGCAGTTTCTTC[A/T]TAGCATCAATGATCT | 84669 |
rs562564493 | snp | C/T | | | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231273 | ATCAATTAACAGTTA[C/T]GTCAATTTCATATTT | 84669 |
rs562577818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358098 | AAATGACTTTTTCCA[C/T]TTAATTGTCTGCTTC | 84669 |
rs562581270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192014 | TATATTTAACGAGAG[G/T]CTTGGCGTGGTGGCT | 84669 |
rs562600884 | snp | A/C | 0.0019968 | 0.0315343 | intron-variant | USP32 | GRCh38.p7 | 17:60292034 | CCAATGACCTACCTG[A/C]AGATCACCAAATTTA | 84669 |
rs562615576 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60339044 | CCTCCCAAGTAGCTG[A/G]GATTACAGGAGCCCG | 84669 |
rs562633008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406254 | GACCATCTCAGCTCA[C/T]TGCAACCTCCGCCTC | 84669 |
rs562644765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60191466 | TGGGAGATGGGGTAG[A/G]GGGGAGGATATAATA | 84669 |
rs562676396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221152 | TAATACCAGCACTTT[A/G]GGAGGCCAAGGCAGA | 84669 |
rs562685771 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256609 | AGGTACTCCGGTTTC[C/T]TCCCACATCCCAAAG | 84669 |
rs562689199 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60206371 | TTATTCTCACTCACA[C/G]TAACCACATCTCAAG | 84669 |
rs562695846 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60220090 | TATAATTCTACTACC[C/G]TCACACCATAAGTCT | 84669 |
rs562702839 | in-del | -/AA | 0.0170251 | 0.090679 | intron-variant | USP32 | GRCh38.p7 | 17:60324552 | GTAAATGGTATGGTT[-/AA]AAGTCACCCTCATTT | 84669 |
rs562704234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404898 | AGAAGCTGTTTGGGT[A/G]GGTGCGATGACTCCA | 84669 |
rs562705636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315271 | CAGGCGTGGCGGTGT[A/G]CGCCTGTAGTCCCAG | 84669 |
rs562714759 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182399 | TTCCATGTCATGTTA[C/T]CTCTCACACCATTGT | 84669 |
rs562719106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339510 | ATTGCTTGAAACTGG[C/G]AGGCGGAGTTTGCAG | 84669 |
rs562723780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259216 | CACTTCTAGGAAACA[C/T]TGAGAAGATAAAGAC | 84669 |
rs562737379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348163 | AAAAAGATGATAAAC[A/T]TTTTTAAGGATACTG | 84669 |
rs562758566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60198809 | AATTAAGGCTCTTTC[C/T]TTCTCCAGAAAATAT | 84669 |
rs562773098 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | USP32 | GRCh38.p7 | 17:60205815 | TTATTGGAAGATTTT[-/A]ATTTTCCAGTTTTAC | 84669 |
rs562811253 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421117 | GAACGTATGTAAAGG[C/T]TCCTTTCCCCTTGCT | 84669 |
rs562830220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316044 | TTCCAGCATCTGATA[C/T]GGGACTTCAAAACAG | 84669 |
rs562842197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411984 | GTCCCTGCATTCAAT[A/G]TAATTTAATATTTAA | 84669 |
rs562842242 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60285747 | AAGAAAAGGTTTCAT[G/T]AAAAAGAGGGTATGT | 84669 |
rs562847489 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420052 | TTTAGTATTTTTATT[C/T]TTATTTTATTTATTT | 84669 |
rs562850330 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60189712 | TGAGATGTGCTCTTA[A/G]GTACCCAAAATGGAA | 84669 |
rs562867201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360972 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCCAG | 84669 |
rs562875704 | in-del | -/A | 0.149665 | 0.228982 | intron-variant | USP32 | GRCh38.p7 | 17:60238804 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs562878153 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60181829 | CTACCTCTGAGGTTA[-/G]CTTCACAACTGTACA | 84669 |
rs562910847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211244 | GAGATGTATTCCTTG[A/G]CCTATTTCATATTAA | 84669 |
rs562912100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60366581 | CGCCATTTTTTAATG[A/G]TAATAGTTCTTGGAC | 84669 |
rs562948202 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60234757 | AATTTTTTTTTGTTT[G/T]GTAGAGATGGAGTCT | 84669 |
rs562974549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60182576 | GAGCCCAGCCTGGGA[A/T]ATATGGCAAAGCACC | 84669 |
rs562984686 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60368807 | TACATATAAGCGAAA[G/T]TGTACAAACATTTCC | 84669 |
rs562993570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347335 | GAATACAGGTGCGCA[C/T]CACCACACCTGGCTC | 84669 |
rs562994263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60273030 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 84669 |
rs563008077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60241788 | TTATCATATATAAAA[A/T]TTGCAAATATTTTCT | 84669 |
rs563015511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381100 | TCAGCTTTCTCCTTT[A/T]AGGAGAAAGCACAGC | 84669 |
rs563023068 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60218578 | GTTAACATAGTCTGA[G/T]AATTTGTGTAAATGG | 84669 |
rs563023785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60397838 | CGTATAGGTATTTAA[C/T]AGTAATTGTGGTATA | 84669 |
rs563028382 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60394734 | ATACTGTAGGTAATT[A/T]TTTATTTATTTATTT | 84669 |
rs563036818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289077 | CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC | 84669 |
rs563039954 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60324801 | TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA | 84669 |
rs563050338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298002 | GTTCTGGCTGGTTTA[A/C]AGAGGCTGCTCACTT | 84669 |
rs563060511 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60357325 | AGGCATGGTGATACA[C/T]GCCTATGGTTCCAGC | 84669 |
rs563074958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327384 | ACCGAAGCAGCCCAT[A/G]GCACAGCTGTCAATG | 84669 |
rs563077779 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60331257 | TTTTGTGAAACAACT[G/T]AAGTACAATAAAACT | 84669 |
rs563089369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327929 | TGGACTTTGGGCACC[A/G]AAAAGCAAGATGGGG | 84669 |
rs563090428 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191983 | TATGGTCTACTGTGC[G/T]TAGAACTGGCAAACT | 84669 |
rs563094358 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60329209 | TACTTCCAGAAAAAA[A/C]CAAAAAGATGTTAGT | 84669 |
rs563106414 | in-del | -/AAAAACAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60261670 | AATAAAAACAAAAAC[-/AAAAACAA]AAAAACAAAAAAAGG | 84669 |
rs563125555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327216 | CTATTTGACATTATA[C/T]ACACGTATCTAAACA | 84669 |
rs563126782 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410243 | AGAAACTGGCTCATC[C/T]GGTCTTGTAACCTCC | 84669 |
rs563166265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60335206 | CTTAAACTCCTGGGC[C/T]CAAGCAATCCTTGAG | 84669 |
rs563193783 | snp | G/T | 1.7318e-05 | 0.00294256 | missense | USP32 | GRCh38.p7 | 17:60181680 | CCAAAGTCCGTGGGC[G/T]GCTATTAGGGCTGCT | 84669 |
rs563200983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60395956 | CTACAACGTGACACC[A/C]ACACATTAAGAGAAT | 84669 |
rs563205409 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60361698 | ACCTATCCTGTATAG[A/C]CTATCTAAGGGTAGC | 84669 |
rs563206430 | snp | A/T | 0.000101887 | 0.00713673 | intron-variant | USP32 | GRCh38.p7 | 17:60288483 | CCAATTATATATATA[A/T]AAAAAGGCAAACAGA | 84669 |
rs563251785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194549 | TAAAGATTGCAGCAC[C/T]CAGTTCACTGTGTTT | 84669 |
rs563253800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185946 | TGGTACATGTCTGTA[C/G]TCCCAGCTACTCAGG | 84669 |
rs563255687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377521 | CAGAATTCATAAAGA[C/T]AGGAGGCATTTCTCA | 84669 |
rs563263737 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60311696 | CAGTTGTGGTGGCAG[A/G]CACTTGTAATCCCAG | 84669 |
rs563271096 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60279450 | TAATTGTACCACTGC[A/G]CTCCTGCCTGGGGAG | 84669 |
rs563276905 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60277298 | AACTCTTTAATGCCA[C/G]AAGTCAATCCTCATC | 84669 |
rs563281263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60255834 | CCATTTTCTTTAAAA[G/T]GTTTAGGTAACTAAA | 84669 |
rs563285007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318512 | AATTCAAACAGCTGA[A/C]CTCTACCTCCATGAA | 84669 |
rs563317628 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60193866 | TGTACTGTCTAGTAC[C/T]ATGTCCAAATCAGGC | 84669 |
rs563334689 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60285073 | GTTTTAACAAATATC[-/A]GAATAATTTTTTCTT | 84669 |
rs563345288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263300 | TTTACCTGTATACTA[C/T]AAACTATCCAAGGGT | 84669 |
rs563366469 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60273684 | CAATAGAGGGCTGGA[C/T]GTGATGGCTCATGCC | 84669 |
rs563387301 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177620 | ACAGATTTTATATAC[C/T]GAAAATCTTGAAACT | 84669 |
rs563405142 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60221665 | GAGTGTGCCACCACA[A/C]TGGATAATTTTTGTA | 84669 |
rs563428269 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394048 | CGTGGCATTAGTCAC[A/T]GCGCTGCCCTTTCCA | 84669 |
rs563434676 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301815 | ACAACAGGCCCTGGT[A/T]AATTTTAGTGAAATC | 84669 |
rs563434898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384257 | CTCCAGACCCTTTCA[A/C]GAGTCATCACCAAAA | 84669 |
rs563437267 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309955 | AGTCTGAGGCAGGAG[A/G]ACTGTTTGAACCTGG | 84669 |
rs563441896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60285711 | TTCAGAGGAATGAGA[A/G]ATAATTTCTGATAAG | 84669 |
rs563451457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60224274 | GGGTGTCACAAGTTA[C/T]ATGGTAAGCACATAC | 84669 |
rs563464148 | snp | A/C | 0.000177582 | 0.00942123 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231560 | CCCACTCGTGGCAGT[A/C]CTGACGACGATCCTC | 84669 |
rs563473269 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60386571 | GTCCTGAGAAAATAT[C/T]TGGCTATGGGTTGGG | 84669 |
rs563475462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60343861 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 84669 |
rs563499395 | in-del | -/AAATTTATCCTGAC | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60312658 | GTTGCCCAGGCTAAA[-/AAATTTATCCTGAC]AAATTTATCCTGACT | 84669 |
rs563503381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60293226 | GTGTTTAAGTTTTTA[C/G]AGTACTGGGTAGCCA | 84669 |
rs563508748 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60308925 | AGAGCAAGACTCTGT[C/G]TCAAAATAAAAAACA | 84669 |
rs563512437 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178432 | TTCCCTCAGCATGGG[C/T]GGGGCCGGGGGTGCA | 84669 |
rs563527909 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60215496 | AGAGTTAAAAAAAAA[A/C]AAAACTCAGTGGAGG | 84669 |
rs563533123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60342750 | GGCACGGGAGAGAAT[C/G]TCCTCTGCTGGTTGC | 84669 |
rs563552339 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422157 | AAGAATTTTACAAAC[C/T]GTGCTTTCCTCTCGG | 84669 |
rs563567150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373951 | ACACTTTGGGAGGCC[A/G]AGGTGGGCGTATCAC | 84669 |
rs563567857 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60351585 | GGCACGCACCACCGT[A/G]CCTGGCTAATTCTTG | 84669 |
rs563584902 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60268090 | TGTTGGGATTACAGG[A/C]GTGAGCAACCATGCC | 84669 |
rs563597019 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60267630 | GGTTGAAGCGATTCT[A/C]CTGCCTCAGCCTCCC | 84669 |
rs563601442 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60210618 | AGCCTACTTCTTTGT[A/G]TTCTACAGATAGAAC | 84669 |
rs563638101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60400610 | TACATTTGAGATGTC[C/T]ATTAGACATCCAAGT | 84669 |
rs563662819 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60275851 | TGAGTAGCTGGGATT[A/G]CAGGCACCTGCCACC | 84669 |
rs563663126 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407767 | AGCCTGGGCGACAGA[A/G]CAAGCCTCTGTCTCA | 84669 |
rs563664319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237827 | CTCGTTTAACCATTC[A/C]TCCACTGATGGATGT | 84669 |
rs563679931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200412 | CTAAAAATACAAAAT[C/T]AGCCAGGCGTGGTGC | 84669 |
rs563703977 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415198 | AAGAGGAGATTCCTA[C/T]CCACTGGGGAGGGCT | 84669 |
rs563714590 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60253640 | GGGTGGTGGCACACG[C/G]CTGTAATCCCAGCTA | 84669 |
rs563734997 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60213102 | GCCACAAAACTTGAT[-/G]GGAAAAGATACACTT | 84669 |
rs563741321 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | USP32 | GRCh38.p7 | 17:60283700 | TAATACCTTTAGGTG[G/T]ATCATGGCAGGGAAA | 84669 |
rs563745760 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60360062 | TTTAGTAGAAACGGG[A/G]TTTCACCATGTTAGC | 84669 |
rs563762940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60224171 | AGTGGTATTTTAAGC[C/G]ATTTCAACTCTCAAC | 84669 |
rs563764368 | in-del | -/AT | 0.00245881 | 0.0349766 | intron-variant | USP32 | GRCh38.p7 | 17:60349667 | TACATATATATACAC[-/AT]ATATATATACACACA | 84669 |
rs563774181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261058 | TACACTGAACAGTCA[C/T]GACTAAAATTCCAGG | 84669 |
rs563774435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60367041 | ACCGTGTTAGCCAGG[A/C]TGGTCTCAATCTCCT | 84669 |
rs563777433 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60257549 | GGCTGGAGTGCAGTG[C/G]TGTGATCACAGCTCA | 84669 |
rs563787811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201186 | TTTGGCTTCTTTCCA[A/T]CAACATTAGGTTTAC | 84669 |
rs563788724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377264 | CAAGAGTTTGAGACC[A/G]GCCTGGGCAACACAG | 84669 |
rs563805961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375352 | CATGGTCATTTTTAC[A/C]GTCCCATACTACTAT | 84669 |
rs563825473 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60376431 | TTTTAAAAATAATAA[A/T]TATTAATTTTAAACA | 84669 |
rs563830726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216903 | ACATTTTAGGATTAG[C/T]TGTAAGATTACAGCA | 84669 |
rs563840631 | in-del | -/TCTC | | | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417339 | ATTTTTGGTGGGGAG[-/TCTC]TCTATGTTGCCCATG | 84669 |
rs563861206 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421086 | ATACATTGTTTACCA[A/G]TCTCACTGCCAGTAG | 84669 |
rs563871745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317635 | GCCTGGGCAAAATAG[C/G]GAGACCCTCACCGCT | 84669 |
rs563874712 | snp | C/T | 1.64914e-05 | 0.00287149 | missense | USP32 | GRCh38.p7 | 17:60223454 | TGATTATCAATAGCC[C/T]CTGGTTTCTGAGGGT | 84669 |
rs563883324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60209708 | ATGAAATCTTTTGAA[A/T]CTTAATGTCAAATGA | 84669 |
rs563888027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261873 | ACACTGACCTCAAAG[A/G]TATGTTAATACTGTC | 84669 |
rs563894430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60215954 | ATCCTCCCACCTTGG[C/T]CCCCCAAAGTTCTGG | 84669 |
rs563905311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423520 | CCAGGCTGGAGTGCA[A/G]TGGCTCAGTCTCGGC | 84669 |
rs563910658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326502 | TTTTGGTAGGGACTG[C/T]TGGCCAGGCTGGTCT | 84669 |
rs563912920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60366690 | AGGATCACTTGAGCC[C/T]AAGAGCTTGAGACCA | 84669 |
rs563936614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231428 | TGATACAGCTTTGGG[C/T]AATTATAAAACCTAA | 84669 |
rs563939919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60241574 | GACAGGCTCTTAGAG[C/T]TACCCACTACATAAT | 84669 |
rs563946883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60230723 | ACTCAGGTTCCTTCT[C/T]CCCCTTCCTACACGC | 84669 |
rs563947384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60376084 | GGGTCTCACTCCTGT[C/T]GCCCAGGCTGGAATG | 84669 |
rs563950290 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60217253 | AGTTACAAAGAATAC[C/T]TACTAAAAGTGCAAC | 84669 |
rs563983627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384463 | AAGGTTTCAAAACAT[C/G]AGTTTTCCTGAATCT | 84669 |
rs563990322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60341741 | TCTCGCGCCATGGTT[C/T]TCAGCTCCATCAGGT | 84669 |
rs564004795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222835 | TACAGGCACACGTCA[C/T]CATGCCCGGCTAATT | 84669 |
rs564017548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60268401 | TAACAAGACACTATC[C/T]CTATTTAAAAAAAAA | 84669 |
rs564019944 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178311 | ACAGAAAAGAACAAC[C/T]ACTAATTGTGAAACG | 84669 |
rs564032847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60193643 | AATAAAGCTGGGGGT[G/T]GGGGAGAAGGAAGCA | 84669 |
rs564071311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60217961 | CAGGCTGGTCTCAAA[C/T]TCCTGGCTTCAAATG | 84669 |
rs564087013 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392481 | GGCGCTTGAGGACGA[C/T]CCCCCCCGCCCCCGC | 84669 |
rs564102913 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60398137 | TGGGCAGCCAAGGCA[-/G]TAGGATTGCTTGGGC | 84669 |
rs564108026 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60334345 | AATTTTATGGTAGTA[C/T]CTGATAAAATAAACT | 84669 |
rs564122910 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60319107 | AGGGGTTGGGAGCAT[C/T]AATGGTTAATGAGCC | 84669 |
rs564129185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60350243 | TGGTCTCAAACTCCT[C/G]AGCTCAAGCAATCCA | 84669 |
rs564136255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268992 | ATGCTACAACATTTT[A/C]GTTAGGTTAAAAAAG | 84669 |
rs564159610 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60288197 | CAAGACTCAGGACTT[C/T]GGGAAACTGAGGTGG | 84669 |
rs564160456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60277770 | TTAGCAAGCTGAATA[C/T]ATTATGATACATTCT | 84669 |
rs564173004 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60276641 | CTTCTGATTAATTGG[C/T]GTTTACATAATACAG | 84669 |
rs564193119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60385265 | CCACTACCCACCCAA[A/C]TCCTATAAAACAGCC | 84669 |
rs564223875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60199821 | CCTCTCATTAAGGAA[C/T]TTCTCCTAGTGCCCT | 84669 |
rs564227901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308856 | TTGCTCTAAACCCAG[A/G]AGGCGGAGGTTGCAG | 84669 |
rs564230321 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393137 | CCAATCCCCCTCCCA[C/G]TGGTCCGTGGCAACC | 84669 |
rs564234884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60292376 | ATATATCAAAAATCA[C/T]ATCTGACAACTCCAC | 84669 |
rs564238541 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177331 | TACAGTTCATATTTC[A/G]GTACATCAACACTAT | 84669 |
rs564239726 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60310269 | AGAAAGGAAATCAAT[A/G]TATCAAAAAGATACC | 84669 |
rs564248919 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60334859 | AGAGATGGGGTTTCA[C/T]CATGTTGGTCAGACT | 84669 |
rs564287017 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60315538 | CCTGGTGGTTCTTCA[A/G]AAAGGTAAACATAGA | 84669 |
rs564290829 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60176854 | GGCATTAGATTCTCA[C/T]AAGGAGCACACAACC | 84669 |
rs564303280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316141 | GACATCAACCACTCT[A/G]CTATCCATGCCAAAC | 84669 |
rs564315978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237708 | TTTTATGTCTGGCTT[C/T]CTTCATTTAACATGT | 84669 |
rs564328855 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413718 | AAAAATACAAAAATC[A/G]GCTGGGCATGGCAGC | 84669 |
rs564336325 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178210 | GGGATGTGTTTTGTT[C/T]GTAATTTATAGCCCT | 84669 |
rs564351459 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60358966 | ATGCAAACCTTAGAA[A/C]CAGAAGGTAGAGACA | 84669 |
rs564370003 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60284466 | ACCTTGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 84669 |
rs564395971 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60381316 | GTGTGGTCCACACAT[C/G]TGGAGTCCCAGACAC | 84669 |
rs564397396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60366486 | GGTCAGGCTGGTCTC[A/G]AACTTCCAACCTCAG | 84669 |
rs564439924 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60283637 | AAAAATACTATCAAC[A/C/T]AGGATATAAAACACA | 84669 |
rs564440866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406524 | TCTTTTGCTTTTTTT[C/T]CTCTTTTTTGAGACA | 84669 |
rs564465168 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60285439 | TGTAATCTGTAGTCA[A/T]GTTATATGTCATATA | 84669 |
rs564466051 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422036 | ACCCAGCACCCAGCA[C/T]GGAGGGCTTATTATT | 84669 |
rs564469799 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60357427 | CCCTGCACTCCAGCC[C/T]GGGCAACAGAGCAAG | 84669 |
rs564473460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414409 | CCTGACTCTAACTTC[C/T]TTGGTGATTGTTTTA | 84669 |
rs564482450 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60215103 | CTCCTGAGTAGCTGG[C/T]ACTACAGGTGCACGC | 84669 |
rs564496015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360024 | AGGCGCCCACCACCA[C/T]ACCTGGCTAATTTTT | 84669 |
rs564507472 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60336277 | TTAAATTTGCTCTAG[C/T]TTAAAACTTGACAAC | 84669 |
rs564508443 | in-del | -/T/TT | 0.171298 | 0.246192 | intron-variant | USP32 | GRCh38.p7 | 17:60228836 | TTTTTTTTGTTTTTG[-/T/TT]TTTTTTTTTTTGGTA | 84669 |
rs564514013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60253595 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 84669 |
rs564526627 | in-del | -/A | 0.0173314 | 0.0914621 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404041 | GAGACCCTGCCTCAA[-/A]AAAAAAAAAAAAAGG | 84669 |
rs564527152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60260940 | AGCTCTGCCACATCA[C/T]GTATCTCAGTCATGA | 84669 |
rs564527541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325146 | CTAGCTGCCACGGTG[A/G]CTCACACTTGTAATC | 84669 |
rs564582385 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60375203 | TGTGGATACCACGCT[G/T]CTTCTTACCCTATAT | 84669 |
rs564588732 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60260317 | CCTGAGGTCAGGAGT[G/T]CGAGAGCAGCCTGGC | 84669 |
rs564598844 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305490 | CAACATTGGGGATCA[C/T]ATTTCAATATAAGAT | 84669 |
rs564628719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305775 | GAGTAAAGCAGTGAG[A/G]GTAAAATTAAGGAAG | 84669 |
rs564630071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308035 | GGCCGCTGAGAGGCC[A/C]GACTCCAGGGGAAAA | 84669 |
rs564663435 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60384503 | GATAGTGATGAGCGC[C/T]GCCCTAGGCCAGGCA | 84669 |
rs564665997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60313382 | TAGTGCAGAGTCCAA[C/T]AGAACAAAATGTTTC | 84669 |
rs564666368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60304843 | ACTCTTATTTTTATA[A/G]TAAAAGCAATAGCTA | 84669 |
rs564666435 | in-del | -/AAAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60333608 | CATCTCAAAAACAAA[-/AAAT]AAATAAATAAAGGTA | 84669 |
rs564667015 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60325824 | GTCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAA | 84669 |
rs564682251 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421367 | GGGCCTCCGGGCTAC[A/C]CCTACTTGAAGCCGC | 84669 |
rs564710671 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60354321 | GCCAAGGCAGGACCA[C/T]GCATTCTGATTTCTG | 84669 |
rs564714446 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403912 | AGGCAGTTTGGCACA[C/T]GCCTGTGGGTCCCAG | 84669 |
rs564717676 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60374289 | GTATTGTCCCACTGG[A/T]AAGTCTTCAGGGCAA | 84669 |
rs564798446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190758 | TTAATAAAAAATATT[C/T]TCCCTTCCTACTTTT | 84669 |
rs564798447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232977 | TTAACTCATTTAATT[C/T]TCACATCCCTACTTA | 84669 |
rs564802359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274347 | CATACAATTGGGATC[C/T]CAGAAAGGGATAGGC | 84669 |
rs564821918 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60369464 | TAACTTTTTACTACA[C/T]TCCAAGATAAATTTT | 84669 |
rs564837282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221817 | ATACCAAAACAAATC[C/G]CACCAAAACATCTTG | 84669 |
rs564841832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362696 | GTTCTAGTTTATTCA[C/T]TTGCTTCCAGCAGTT | 84669 |
rs564843066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403241 | CAGGATGGTCTTGAT[A/C]TCTTGACCTCGTGAT | 84669 |
rs564844026 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256654 | TTAACAGGAGTGTCT[A/T]AATTGTCCCACTGTA | 84669 |
rs564854877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60250148 | AGGTCCTAAACTTGA[C/T]TCTGCCAGTCCCATG | 84669 |
rs564859661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280106 | TATTATTATTATTAT[G/T]ATTTTTTGAGATGGA | 84669 |
rs564880010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212675 | AAGTAATTAAAGTTC[A/G]GAAACAATGGAATTT | 84669 |
rs564882038 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403717 | AACTATATATTTTTT[C/T]ACACATATATATTTG | 84669 |
rs564894237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60321141 | AGAAGCTCAGGAAAG[C/T]TGTCTTTTGAACTCC | 84669 |
rs564901378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410394 | CCTAGCCTCGGTGGG[C/T]GCGGTGGCTCATGCC | 84669 |
rs564944047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60248562 | TTCTTTCTCTCTTTC[A/T]GATGAAATAATCTCT | 84669 |
rs564956724 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60363226 | TTGGGAGGCTGAGGC[G/T]GGCAGATTGCCTGAG | 84669 |
rs564974735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60287882 | ACTTCGGGAGGCCGA[A/G]GCGTGTGGATCACGA | 84669 |
rs564984238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60371428 | AAAAATCAGCCAGGT[A/G]CGGTGGCACACGCCT | 84669 |
rs565030308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402598 | AGTAATCAGAATCAC[A/G]TTCCAGCACAGTATG | 84669 |
rs565033928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418238 | GCTGGGATTACAGGC[A/G]TGAGACCCCTCGCCT | 84669 |
rs565034968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60220143 | TATATAAATGATTGA[C/T]ATTTTAAGGACAAAT | 84669 |
rs565040447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60203887 | GCCTTTCCTTTACTT[C/T]ATAAAATTAAGACAC | 84669 |
rs565053290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60180422 | TACTGACAGCATCTA[C/T]ATATTGATTCTAACA | 84669 |
rs565055658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60270354 | TAGTATATTCCCAGA[A/G]TCTAACGCAGTGCCC | 84669 |
rs565056207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256865 | AACTTATTATTCCTC[A/G]CAGATTTCTATTCTC | 84669 |
rs565067363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60402024 | AAGGGTGCTAACTTA[C/T]CCCAGATCTTCTAGT | 84669 |
rs565086382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60386747 | TCACTAACCAGCAAG[G/T]GATGTCCCCTCATTT | 84669 |
rs565094570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320660 | CATTATAATGAAAAA[C/T]AACACCGAATGAGTG | 84669 |
rs565095642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60219469 | GACCATAGTTCTAAG[A/C]CCTGTAAAAATTAAT | 84669 |
rs565106687 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378400 | AGCTGTTCCTTAAAG[C/G]GTTAAATATAGAATT | 84669 |
rs565114788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60328211 | TACTTCCTCCCCTCT[G/T]AGGCCCATAAAAGCC | 84669 |
rs565115943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60247465 | GATTACAGGCATGAG[C/T]CACCTCGCCCAGCCT | 84669 |
rs565131390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60233684 | TTTTAGAAAAGAACA[C/T]TTTTCTAATTAAAAC | 84669 |
rs565139316 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60240032 | GGGCCACCATGCCCA[A/G]GCCAATTCTCCTGGT | 84669 |
rs565144273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407910 | CGAGACCAGCCTGGC[C/T]AACATGGTGAAACCT | 84669 |
rs565147922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271130 | TATACATGAGCATGC[G/T]CGGGTGCAGAGAGCT | 84669 |
rs565153122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60379005 | TATGTACATACCTGA[A/G]TTTGTGAAGATCAGA | 84669 |
rs565167668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60188351 | CAGGGAATCCTTTTA[C/T]ATTCTTAATTATATT | 84669 |
rs565171350 | snp | C/G | | | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419363 | CACTGGGGCCTACCA[C/G]AGAGTGGAGGGTGGG | 84669 |
rs565182607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60255678 | AACTAGTTCAAGTTC[A/G]TTCCTGTATGTTTTC | 84669 |
rs565200308 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60400897 | CTTGATATGGTGCCA[A/C]CTGTGATCCCAGCTC | 84669 |
rs565209910 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60218866 | TCCCAAATTGTGGGA[C/T]TACAGGCATGAGCCA | 84669 |
rs565211391 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60368747 | CCTAATAATCATACA[C/T]GGTTCTATACACAAC | 84669 |
rs565222313 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | USP32 | GRCh38.p7 | 17:60210311 | CATTCATCCTTCTAC[-/T]TTTTTTTTTTTCTTT | 84669 |
rs565228068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60329007 | GAGCCTGCCAGGCCA[A/G]GTGGATGGAAAAAGC | 84669 |
rs565233366 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60244835 | CGAGGTTTTGCCATG[C/T]TGGCCAGGCTGGTAT | 84669 |
rs565236333 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416268 | AGGGAAAGCGTAAGC[A/G]GTAGATGCTAAGAGT | 84669 |
rs565236422 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60394826 | TCGGTTCACTGCAGC[C/G]TCTGCCTCCCAGGTT | 84669 |
rs565249604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60368102 | AGACACCAAGGGACT[C/T]CTGTCCTTCAAAGAG | 84669 |
rs565254554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337506 | TATTAATAAATCAAA[C/T]ATTCGCTAAGTATAT | 84669 |
rs565271664 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412402 | CCAGCTACTAGTGGG[A/G]AATGGGGGCGGTGGG | 84669 |
rs565276619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225569 | TTTTACAATTGACCA[C/T]TTCATTCAAAACTTA | 84669 |
rs565289286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232885 | ATATAACTACTGCTA[C/G]TACTACCACCATTAT | 84669 |
rs565293774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60336454 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 84669 |
rs565299217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60179530 | TAATTACTAAACCTG[A/G]TTGCTTCCAATAAGC | 84669 |
rs565310336 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60294318 | CTCAAGGCTAATGAA[C/T]GAATGATATCCGTGA | 84669 |
rs565316811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60238764 | AGTCGAGATCATGCC[A/C]TTGCACTCCAGCCTG | 84669 |
rs565328698 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60344580 | TCAGCCTCCTGAGTA[A/C]CTGGGACTTACAGGC | 84669 |
rs565331298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60344789 | TCTCATTTAGAATGA[C/G]AAAATGTACATCTGT | 84669 |
rs565363763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60352302 | CTGGCACTTAGATAT[A/G]CAATGGCTGCATCTC | 84669 |
rs565366141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353388 | TTTTGTGATGGTAGC[C/T]CAAGCTGACTACTAT | 84669 |
rs565369383 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60247916 | GTCTCAACCTCCTGA[C/T]GTCATGATCCACCTA | 84669 |
rs565376637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60239046 | TTTTGGTGCTACAAC[A/T]AACATTCCACTGCAA | 84669 |
rs565391159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295188 | AAACTCTGAAACCTG[C/T]GTACAAAATACAAGA | 84669 |
rs565402730 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60360632 | GTGAGCTGAGATTGC[A/G]CCACTGCACTCCAGC | 84669 |
rs565409963 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60182696 | TGACCCCAGGAGGTA[A/G]AGGCTGCAGTGAGCT | 84669 |
rs565424691 | snp | G/T | 1.70475e-05 | 0.0029195 | intron-variant | USP32 | GRCh38.p7 | 17:60211153 | ATTTGTTGCCAAAGA[G/T]TCTCATAAATCACAA | 84669 |
rs565424863 | in-del | -/AGTA | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60388883 | CTTCCACTCAGGCCC[-/AGTA]AGTGTTATCTGTCAT | 84669 |
rs565428705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302691 | AATAATGTGATAAGA[A/T]TTTTGTGCAATTACA | 84669 |
rs565431502 | in-del | -/TTTG | 0.292266 | 0.246401 | intron-variant | USP32 | GRCh38.p7 | 17:60302106 | CATATATATAAATAT[-/TTTG]TTTGTTTATTTATTT | 84669 |
rs565436620 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60363180 | TTTTTTGAGGCCAGG[C/T]GCGGTGGCTCACACC | 84669 |
rs565449691 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60202639 | ATATTTTATTTTCTA[C/T]ATAGATGTCTTATGT | 84669 |
rs565449751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194789 | TCCTATCTTTTTGGG[A/T]TACTTACTTATTCGA | 84669 |
rs565456199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60275668 | TTAAGTTACCTGGAA[A/G]GATAAGAACAAAGTT | 84669 |
rs565479664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60202141 | GGATATCTAATTGTC[C/T]CAGCACCACTTGCTG | 84669 |
rs565480383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416130 | GGTGTGACCCACTGC[A/G]CCTGGCTTACTCTTG | 84669 |
rs565481189 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415457 | CTAACTTCCAGAATC[A/C]CTGCCGAGAAGGTCC | 84669 |
rs565491832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210608 | CCCTGCGCCCAGCCT[A/C]CTTCTTTGTATTCTA | 84669 |
rs565492556 | in-del | -/TATT | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60344987 | TTTTTAGAAACAGAA[-/TATT]TATATCAACTTAGCA | 84669 |
rs565496164 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60201444 | TAACTAGAAAATTGT[A/T]TTCCAAAGTAGTTGT | 84669 |
rs565510454 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60298812 | GGTTTACTGGGCATA[C/T]ACACGTGTCAAAACA | 84669 |
rs565514919 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60357967 | GAGATGGGGTTTTCA[A/C]CATGTTGGTCAGGCT | 84669 |
rs565517462 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60234587 | AAAAAAAAATTAGCC[A/G]GGCGTGGTGGCACGT | 84669 |
rs565548854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60401498 | GGGCTATCAATGTGC[A/G]ATACTTGACAGGAAG | 84669 |
rs565560044 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60210255 | TCACTAAAATCTACT[A/G]CATCTGATATTAATA | 84669 |
rs565560274 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60201762 | CTCTGGGGTTCAAGT[A/G]ATTCTCCTGCCTCAG | 84669 |
rs565594402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222842 | ACACGTCACCATGCC[C/T]GGCTAATTTTTGTAT | 84669 |
rs565598694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327319 | GCAGTGGTGGCAGGA[C/T]TGGCTTCAAGAGCAG | 84669 |
rs565605591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60361510 | CTCCTTAGATACATA[C/T]AGAGAGTGCTTCTCC | 84669 |
rs565605774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60310590 | TATAGTCCCAGCTAC[A/T]TGGGAGGCTGAGGCA | 84669 |
rs565614503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424250 | ATGAGATTTAGAGGG[A/G]ACACACATTCAAACC | 84669 |
rs565630584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286844 | ATGCTCACCATCCTT[C/T]TTTGTTCTAAATTTC | 84669 |
rs565630669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295483 | CAAAAATATTAAATG[G/T]AAATTTCCAGAAATG | 84669 |
rs565640344 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402303 | TTGCCCAGGCTGGAG[G/T]GCAGTGGTGCAATCA | 84669 |
rs565709644 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60278210 | ACCCAGACAATAAAT[-/A]AAAAATTTTAAAAGC | 84669 |
rs565715202 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60326859 | CTGCCAAGTTATTTT[A/G]TTGTTAAAAAATAAA | 84669 |
rs565748099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60195005 | GAACTATACAATGAA[C/T]ATCCCATGTATTCAT | 84669 |
rs565758119 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177794 | TTAATAGTTACTGGC[C/T]TCAGATATCAGAACA | 84669 |
rs565765591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254770 | CTCCTTATGATTCAT[C/T]TTTCTGGTCATACTG | 84669 |
rs565771833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360850 | ATACATAAAGTAGGC[C/T]GGGCGCGGTGGCTCA | 84669 |
rs565793635 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60255314 | TTTTTTTTTTTTTTT[C/T]TGAGACGGAGTCTCA | 84669 |
rs565794914 | snp | A/C | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177041 | GTTCCTAACAGGCCA[A/C]AGATGGTACTGGTCT | 84669 |
rs565820633 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60367645 | AAACCCCATCTCTAC[C/G]AAAAATACAAAAATG | 84669 |
rs565824244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416454 | AACAACCCACAACCC[C/G]CTCACCTGCCAGATG | 84669 |
rs565825872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186017 | GTGATTACACCACTG[C/T]GCTCCAGCCTGGATG | 84669 |
rs565826250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408158 | TCCAATAAAAAATTA[C/T]TATTTATACCAAGAA | 84669 |
rs565831808 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378915 | TTCAAATGGTAAATG[G/T]TATGTTCTATATATA | 84669 |
rs565872163 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60329112 | CAACACTGTACTCCA[C/T]AAATATGTATAATTA | 84669 |
rs565905333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407488 | TAGAGTAAAGTACAC[A/G]CTAGAACTGCTTAAT | 84669 |
rs565913957 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60368324 | TAGAATGAAATACAC[A/T]TTAGATTGCTTTTTA | 84669 |
rs565946975 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60301168 | TGTACAAGTTTTTTT[G/T]TGTGTGTGTGGTAAA | 84669 |
rs565950281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222958 | AAGTGCTAGGATTAC[A/C]GGCATGAGCCACCAC | 84669 |
rs565957862 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60197111 | ACTTGAACCTGGAGG[C/T]GGAGTTTGCAGTGAA | 84669 |
rs565964034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377809 | TTTTAGAGTAGGGTT[A/C]TTTCTATTCTGGTTT | 84669 |
rs565975567 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP32 | GRCh38.p7 | 17:60226759 | GAAGGGCAATGCTAT[A/G]ACTTATACCTATGTG | 84669 |
rs565980045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268670 | CAGTTTGAAATAGTG[C/G]TATAACAACAGGGAA | 84669 |
rs565999030 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60217428 | CCCTCCCGAGTAGCT[C/G]GGATTACAGACACCT | 84669 |
rs566002587 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60376820 | GCCACCACACCTGGT[A/C]AGAATGTTGGGAAAA | 84669 |
rs566015979 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60276293 | TGCTGAAGTATCTAC[C/T]TCAAATATCCAGATA | 84669 |
rs566029383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60277231 | TCTTGGTCTGCACTT[C/T]GGGCCATCCTAATCA | 84669 |
rs566037729 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308436 | CACACACCCTGTGAG[A/G]GGGACAAGGGAACCT | 84669 |
rs566038622 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60338896 | TTAGAAGTACATAAA[A/G]ATATTTTCTTTGTTT | 84669 |
rs566047420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261201 | TGACAAAATTAACAG[A/C]TAGTGTAAACCCATT | 84669 |
rs566057843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60300360 | AAAAGTAAATAAATC[C/T]ATATCCCACGAAACA | 84669 |
rs566062499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223746 | AGGAAATGTTATCCT[C/T]CTCTGAACAATACAT | 84669 |
rs566091192 | snp | A/C/T | 3.5504e-05 | 0.00421319 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231572 | AGTCCTGACGACGAT[A/C/T]CTCGAGGGCTGCTCT | 84669 |
rs566091401 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60277949 | TTGAAGAGACAGGGT[C/G]TCACTCTGTCACCCA | 84669 |
rs566112744 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296751 | ATTAGTTACAGAACC[C/T]CCAAGGACACCAAAA | 84669 |
rs566119553 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60342840 | CTGACATGGATTCCC[A/G]TGGCTAGGAAAGGGA | 84669 |
rs566194628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60244076 | AGTCTAGCTCTGTCA[C/T]CCAGGCTGAAGTGCA | 84669 |
rs566197048 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60400799 | GCTGAGTCGGGGGGA[A/T]CACTTGTGGCCAGGG | 84669 |
rs566198185 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60320534 | TCAAACGTGCACACC[A/G]TTGGGATGAGGGAAG | 84669 |
rs566201075 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60341460 | TGGATATGAAATTCC[A/G]GGTTGAAAATTCTTT | 84669 |
rs566206527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281970 | CCATAGTAGACTTAC[A/G]GCTGACTTGTTTTTA | 84669 |
rs566213874 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306127 | CTATTTAAATGGTCA[C/T]CTTATAATAGGCAGT | 84669 |
rs566214012 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60392075 | CCCACACTAACAAGT[C/G]CGGCTTCTGCCCCGG | 84669 |
rs566229909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192722 | GAGCCACCGTGCCCA[C/G]CCACAATTCTTAAGT | 84669 |
rs566240906 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60281296 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG | 84669 |
rs566262740 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60237397 | TTGGGATTACAGACA[C/T]GAGCCACTGTGCCCA | 84669 |
rs566270531 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60351624 | GTAGAGGCGGGGTTT[C/T]GCCATGCTGGCCAGG | 84669 |
rs566301855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244850 | TTGGCCAGGCTGGTA[C/T]CGAACTCCTGGCTTC | 84669 |
rs566304967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60288873 | AAATACTTGTGCTTC[A/G]TAACTTCTACTTGCA | 84669 |
rs566310490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60273325 | TAGAGCTCATACAGG[A/G]CTGGGAGATGTCTGA | 84669 |
rs566313948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60253682 | GAGGCAGGAGAATCG[C/T]TTGAACCTGAGAGAT | 84669 |
rs566316443 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60201147 | ACAGGTGTGAGCCAC[C/T]GTGCCTAGCCTAATT | 84669 |
rs566343674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221336 | AGCTTGAGGTTATTT[G/T]TCATAAACGTAATTA | 84669 |
rs566358039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60331355 | CGGACTGCTTGAGTC[C/T]AGGAGTTCAAGACCA | 84669 |
rs566371293 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60366748 | TCAAAAAAAAGTTGG[G/T]TTTTTTTTTTTCATG | 84669 |
rs566381007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358764 | ATGAGACCAGGATAT[C/T]GAGGATGACGGTGCT | 84669 |
rs566410390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60309180 | TCAGCAAAGGCAACA[A/T]TCAATAAAATTAAGA | 84669 |
rs566418088 | snp | C/T | 1.67609e-05 | 0.00289486 | synonymous-codon | USP32 | GRCh38.p7 | 17:60208799 | ATCCACAACAATTGA[C/T]CTATTTCTTCTTAGA | 84669 |
rs566438059 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392814 | TTTTCGGGTCATCTC[G/T]CCTGCCCGGCCCACC | 84669 |
rs566446270 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60322149 | GTTCTTTAAAGTGAA[A/C]TGAGTAGGTAACTCT | 84669 |
rs566447540 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60257672 | AAAAACACAGAAAAA[C/T]AAGGTCTAGTTATGT | 84669 |
rs566450295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60181998 | GACTCAGAAAATAGC[A/G]GAAAGATGATTTATG | 84669 |
rs566464835 | in-del | -/TCTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60237161 | CTATCTATCTATCTA[-/TCTA]CAGAATCTCACTCTA | 84669 |
rs566470836 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60220792 | GGGAATACAGGAGCC[C/T]GCCACCACGCCTGGC | 84669 |
rs566471979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410497 | CACGGTGAAACCCTG[C/T]CTCTACTAAAAATAC | 84669 |
rs566479733 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60397215 | CAGTTTCTAGATAAT[A/G]ATAACTTTGTCAAGT | 84669 |
rs566482354 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60289787 | TCAGGAAAAAAAAGA[A/C]AGAAATACATTGAAT | 84669 |
rs566484434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228256 | CCTGAACACAAGTGA[C/T]CCACCTGCCTTGGCC | 84669 |
rs566517252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330672 | CAGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 84669 |
rs566542842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227371 | ACCTCCCAGGTTCAG[C/G]AGATTCTCCTGCCTC | 84669 |
rs566546450 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60234889 | TTAAGTAAATTTTAA[A/T]GTTTGCATTTGACAG | 84669 |
rs566560247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60272653 | ATAAGCAGCATAGAA[C/T]GGTGAACCTTGAGAG | 84669 |
rs566577562 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60381697 | TGTTGCTTTCTAGAT[-/C]TTGAAATGTTCTGCA | 84669 |
rs566579521 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60188274 | GAGTGATTGCCTCTG[-/T]TTTTTTTTCTGATTA | 84669 |
rs566588676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388399 | GAAGAATTAAAAAAC[C/T]GGTGAAGATTTTTAA | 84669 |
rs566619526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60264222 | TCCTTACCACAACCA[C/T]TTAAAAAAATTTTTT | 84669 |
rs566628645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263679 | AGGCATTTTCTAACA[C/G]AAACTTTTCCTGGTT | 84669 |
rs566646259 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60379421 | GATTTAGGGACTCAG[C/G]ATACTAAGATAAACA | 84669 |
rs566664549 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60347635 | TGGGATTACAGGCGT[A/G]AGCCACCGCGCCCGG | 84669 |
rs566664608 | snp | A/G | 1.6693e-05 | 0.00288898 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179246 | TGTCTAGCAGCCAGA[A/G]TGGTAGCTTTACTGT | 84669 |
rs566677709 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306010 | ATGTACATATTTTCC[A/G]CCTTTAATCAATGTT | 84669 |
rs566699480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60346707 | TCACAATAGAGGCAC[A/G]GAAATGGTACCTTTG | 84669 |
rs566732716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418480 | TGTTCTGTCACCAAA[A/C]GCAGTTTCAACAAAA | 84669 |
rs566738172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355628 | GAAGCAGATGAATTG[C/T]TTGAGCCTAAGAGTT | 84669 |
rs566775488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212257 | GAGGTTATATTCTGA[A/G]AAATGCATCATTAGG | 84669 |
rs566806414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60297209 | TCGAGACCAGCCTGG[C/G]CAACATAGCGAGACC | 84669 |
rs566818575 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60364578 | GACAGGGTTTCACCA[C/T]GTTGGCCAGACTGGT | 84669 |
rs566819872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204936 | ACACCATCATGGCTG[C/T]TTAGTTAAAAAAAAG | 84669 |
rs566821576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60386965 | CCATTTTTCTCCTTT[A/G]CAAATAGTAAGATCT | 84669 |
rs566830150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401263 | TAGTCCCAGCTACTC[A/C]GGAGGCTGAGGCAGG | 84669 |
rs566836317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60313656 | AGAAGAGACACCTCA[C/T]TGAACATCCAGAGCA | 84669 |
rs566876454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417704 | AGTGATCCGCCTGCC[C/T]CAGCCTCCCAAAGTG | 84669 |
rs566887090 | snp | C/T | 2.2089e-05 | 0.00332325 | intron-variant | USP32 | GRCh38.p7 | 17:60219608 | AAATGCATGGTATTC[C/T]TGCTGCATTCTTAAG | 84669 |
rs566896964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362801 | TAGTTCAACTATATT[A/T]AAAAATGTTTCCAAG | 84669 |
rs566921345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60330442 | TAACTTAGATTTCTT[C/T]CTTTTCTTTTCTTCC | 84669 |
rs566934621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60261374 | AATGTAGGCCAGGCA[C/T]GGTGGCTCACACTTG | 84669 |
rs566967949 | in-del | -/TTTGTTTTTTTTGTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60228818 | AACAGAGCGAGACTC[-/TTTGTTTTTTTTGTT]TTTGTTTTTTTTTTT | 84669 |
rs567007474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211695 | AGTGTCTGGCAACAG[C/T]GATGATCCATGCTCA | 84669 |
rs567012043 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60362865 | AACAAAAAACACCTT[A/G]GTCAAAAGGCAGCTA | 84669 |
rs567019246 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60270779 | AGTGAGCCGAGATGG[C/T]GCCACTGCACTCCAG | 84669 |
rs567024663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60189081 | TTGTCATCATTGACA[C/G]TAATGTCTTGTCAGA | 84669 |
rs567046296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320292 | AATAAATACCCCAAA[A/G]CATTTCTAATATTAA | 84669 |
rs567052440 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60385580 | GAAGCAGTGGCTCAC[A/G]CCTATAATCTCAGCA | 84669 |
rs567054084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218993 | ACCTTACAGAGAAAT[A/G]AAAGGGGAACTTTTT | 84669 |
rs567057192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60187794 | CCTCTTGGGATCTAC[A/G]CTTAGATCCTCTACT | 84669 |
rs567068230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60328527 | CACCCTCCATCTGCA[C/T]ACCTCATTCTTCCTG | 84669 |
rs567107971 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60187480 | AAAGGAAACGTGCTG[A/C]ATCATCGTTGTTGGA | 84669 |
rs567132669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305094 | CCAACTTTTAGTTCT[A/G]TAGTACAATTAATAT | 84669 |
rs567138006 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411103 | GGAGGCCGAGGCAGG[C/T]GGATCACCTGAGGTT | 84669 |
rs567182886 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60338444 | AGACAATTCAGAGTT[C/G]GTGAGGCCAGGCATG | 84669 |
rs567197364 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60322170 | AGGTAACTCTATAGG[C/T]CAAACTTTTTTTTAA | 84669 |
rs567204023 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60388744 | TAACAGTGTTTAAAT[A/G]TACACTTTTAGAAAA | 84669 |
rs567210272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60287569 | TATGTGATTTTTACT[A/G]AGCCAGGTAAGCAGA | 84669 |
rs567216372 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178991 | TATTTGGTCCCAGGT[A/G]GCTGGTGCCAAACCT | 84669 |
rs567216736 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60292873 | AGTCAAAGGACTCAC[A/G]CTGTCCTATAGGACA | 84669 |
rs567219500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60346349 | AATTAGCAGGTAAGC[C/T]AAATGCCACTGGATT | 84669 |
rs567230099 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60288755 | ACCTGCACAACCTGA[A/G]ATTTGCAATTAGTTG | 84669 |
rs567239427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60349412 | TGGTGAAATCCCATC[C/T]CTACTAAAAATACAA | 84669 |
rs567271850 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60261962 | CATACAATGATGATC[-/A]AAAAGCCCATTTGCT | 84669 |
rs567273606 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60234429 | AAGCATGACTAATTT[A/T]AAAAAAAATTTTTTT | 84669 |
rs567276971 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60325842 | GCTGAGGCAGGAAGA[C/T]TGCTTGAGCCCAGGA | 84669 |
rs567283311 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60298548 | TTTCTTATTTGTATT[-/A]TTTTTTTTGCTGTAC | 84669 |
rs567287081 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195139 | TTTTAATGTCCGAAG[G/T]ACATAACCCACTCCA | 84669 |
rs567325736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337936 | ATTAGTGAATGGGCC[A/C]TTATCTAATAAAATG | 84669 |
rs567334430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234044 | AGTCTTGACCTATCA[G/T]GCTCAAGCAATCCTC | 84669 |
rs567336156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60280575 | TAAAGGCATCTGCAT[A/G]TTAACATGTTATTTA | 84669 |
rs567342790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60241159 | TGCGCCACCATGGCC[A/G]GCTAATTTTTTGTAT | 84669 |
rs567365159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60395975 | CATTAAGAGAATTGA[C/T]TTTTCAGTATTATGG | 84669 |
rs567375673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355414 | AAAAAAACCTGTAAG[C/G]AGACCGATTGCCGGA | 84669 |
rs567383124 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60290758 | GGGCTGGCCACTGGG[A/G]AAAAAAAAAAGAAAA | 84669 |
rs567395608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288243 | CCAAGAGTTCAAGAC[A/C]AGCATAGGCAATATA | 84669 |
rs567398894 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60248701 | TGGACAAGTCAGTGA[A/G]ATCATACATTCCTCT | 84669 |
rs567399155 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60183507 | TTCTGAAGATACAAA[A/G]TTTACATGGAAAAAA | 84669 |
rs567409078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60256958 | CTAAGAAATATATTG[A/G]TAAGAACACACATGC | 84669 |
rs567418832 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60270572 | CTCACGCCTGTAATC[C/G]CAGCACTTTGGGAGG | 84669 |
rs567425059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60269726 | TTCCTCTTGGTATAA[C/T]TATAATTGAAACTTG | 84669 |
rs567425461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60203972 | AGGTTGCTAAATTCC[C/T]AGTTCAGTGCCCTTT | 84669 |
rs567455151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60240518 | AGAGAGAGAGACAAA[A/G]GACAGAGACAAAGAC | 84669 |
rs567466353 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409834 | AATGATAGCTCATAA[C/G]CTTAAAAAAATCACA | 84669 |
rs567466930 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60370395 | TACTCAATTAGCAAA[A/G]AATTTTTTGCAAATG | 84669 |
rs567469218 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60252893 | AGATAGAAAATAAAA[A/G]CAATTTAGCATAACT | 84669 |
rs567495654 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60312746 | TTCCAAAGAACTTGA[A/T]GTCACCAACCTACAT | 84669 |
rs567510962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354370 | CGTTTTAACAGTTTG[G/T]TTCCAAAGGCAAAGA | 84669 |
rs567513846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60247851 | ATCACACCTGGATAA[C/T]TGTTTTGTATTTTTA | 84669 |
rs567528302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196092 | GCCAACATGGTGAAA[A/C]CCTGTCTCTACTAAA | 84669 |
rs567535759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320822 | CATGTACAATGATTA[C/T]CAGAATTCCAGGCAA | 84669 |
rs567575133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256508 | ATTTTATTATAATGT[A/T]AATGGGGGAAAAAAT | 84669 |
rs567585434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60361676 | ACTTTTTAAAAATTA[C/T]AGAAGAACCTATCCT | 84669 |
rs567605715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369356 | AGCTACTTGGGAGGC[C/T]GAGGTGGGAGGATCA | 84669 |
rs567609367 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60212171 | ATTGCTTTTTTTTTT[A/T]AAAGACATCTTATTC | 84669 |
rs567620833 | snp | A/T | 1.65042e-05 | 0.0028726 | missense | USP32 | GRCh38.p7 | 17:60211461 | GGATGCTTGAGTTCA[A/T]GAAGCATGTGTTTCC | 84669 |
rs567634646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60311912 | CTGCTGCTTTCTGGT[C/T]CTGGTCATTCCACTG | 84669 |
rs567662770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60279345 | TTAGAAATTAGCCGG[A/G]TGTGGTGAATGCACC | 84669 |
rs567681584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218947 | TGCAAAGCAAAAGCA[C/T]AGAGCAAGTCTTGCC | 84669 |
rs567699192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413212 | ATGTGTTCTGTATCC[C/T]GCCAGTGGGGGAGGG | 84669 |
rs567718843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60328378 | AGGATGGGATGACCA[A/G]CTGAAGAGAAAAGCT | 84669 |
rs567726508 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60287336 | AAGCTCCCCTTTCAA[C/G]ATATCTGGCCCTTTT | 84669 |
rs567738328 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60401734 | AAAAAAAGAAAAAAA[A/G]AAAAAGAAAGAAAGT | 84669 |
rs567738966 | in-del | -/GTG | 0.00120749 | 0.0245415 | intron-variant | USP32 | GRCh38.p7 | 17:60401230 | GGGGCCAAGGTGGGC[-/GTG]GTGGTGGTGGGCGCC | 84669 |
rs567778098 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60366210 | GTCGCCTAGGCTGGA[A/G]TGCAGTGGCGCGATC | 84669 |
rs567786330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218245 | AAAAATGAGCCAGGT[A/G]TGGTGGTGGGCGCCT | 84669 |
rs567798523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60179649 | ACAAGTCAAAAAAGA[A/G]TGACCTAAAACCTCA | 84669 |
rs567805018 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60267329 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 84669 |
rs567838327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60224767 | CAGCCTGGGCAACAG[A/T]GTGACACCCTGTCTC | 84669 |
rs567853815 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | USP32 | GRCh38.p7 | 17:60336582 | TTAGCCGGGCGTAGT[G/T]GCGGGCGCCTGTAGT | 84669 |
rs567861301 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402268 | TTTTTTTTTTTTTTT[A/T]AATACAGAGTCTCAC | 84669 |
rs567897857 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413884 | AAAAAAAGAAAAAAA[A/G]AAAAAAAAAAAGAAT | 84669 |
rs567918396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60343865 | GGTGAAACCTCGTCT[C/T]TACTAAAAATACCAA | 84669 |
rs567929724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286808 | GATCAGACCTTAGAC[C/T]ACAGGGGAACTAAAG | 84669 |
rs567961169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186159 | TCTGGATAAAATTTC[C/T]ATTTATATGACCATA | 84669 |
rs567976576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235807 | AGCACCAGGTTCCCC[A/C]CAGGTAAAATGGGTA | 84669 |
rs567981505 | in-del | -/G | 0.00250365 | 0.0352924 | intron-variant | USP32 | GRCh38.p7 | 17:60240660 | GAGGTGAAAGTTTAC[-/G]GGTCTTATAAGGTCT | 84669 |
rs567997770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265203 | AAAATGCCTAGCTTA[C/T]AATAAATGTTTTCAC | 84669 |
rs568003859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60294422 | TGTATTACTGTGTTA[A/G]TGTGAGTATATAGAA | 84669 |
rs568009016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390245 | GAGCTGAATACAAGT[C/T]TAATTTTGGAATTTC | 84669 |
rs568014121 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60385038 | AATACATTCAGATGG[A/C]CTGAAGCAACTGAAG | 84669 |
rs568014164 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60207894 | GGTAGAAAACTCTTA[A/G]GTTTCTGGGTTGGAA | 84669 |
rs568030216 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60262683 | TCTACAGCCTTCAAT[-/A]ATATGAATCTGTTAT | 84669 |
rs568031593 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant, missense | C17orf64, USP32 | GRCh38.p7 | 17:60422331 | TGCGCTCTGCCAAAG[G/T]CTTCGCTCGACCCCG | 84669 |
rs568046624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60374747 | TAGTAAATGACTACA[G/T]AAAAAAAGCAAAAAG | 84669 |
rs568050123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60316734 | TAGTCCCAGCTACTC[A/G]GGTGGCTGAGGCAGG | 84669 |
rs568076711 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60215460 | AAATGAAATAAAACT[C/T]AGTGAAAAAAAAATT | 84669 |
rs568100318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243320 | ATTACAGACAGTTTT[A/C]TTTTTCTTTACAATC | 84669 |
rs568121671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325256 | CTGTCTCTACAAAAA[A/C]TACAAAAATTACCCA | 84669 |
rs568130375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274641 | AAAACAAAATTGTCA[A/G]CCTCCAATTCTGTAT | 84669 |
rs568141304 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418339 | CTCAGGCAATCCACC[C/T]GCTTTGGCCTCCCAA | 84669 |
rs568153003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60242597 | TGTGTTTTTAGTAGA[A/G]ATAGGGTTTCGCCAT | 84669 |
rs568153053 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60275290 | GGTGAAACGCCATCT[C/G]TACTAAAAATACAAA | 84669 |
rs568175658 | snp | C/T | 8.25743e-05 | 0.00642498 | intron-variant | USP32 | GRCh38.p7 | 17:60222566 | TGAGAAAGAATAGAA[C/T]GACAATGTTGACTTT | 84669 |
rs568183021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356698 | CTTAAGGTAGGGAAT[C/G]CAATTTCCAGAGCTG | 84669 |
rs568190313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60214837 | AAGCACCCCTCTCAG[C/T]AATGGGGACCATACT | 84669 |
rs568197211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60365251 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCATGAGG | 84669 |
rs568221203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60364490 | GTTCAAGTAACTTTC[A/G]TGCCTCAGCCTCCCA | 84669 |
rs568222161 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60229057 | ACTTATGCTTTTTGA[-/T]TTTTTTAGTCTGGAG | 84669 |
rs568224781 | in-del | -/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403018 | GGGTAAGCCGTATCT[-/C]TGTTTTTTTTTTGAG | 84669 |
rs568233937 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60229668 | GTCACTTTGTTTTCC[A/T]CCAGAAAAATCACTT | 84669 |
rs568237435 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60270550 | AACAGCAGACTGGGC[A/G]CAGTGGCTCACGCCT | 84669 |
rs568245307 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265949 | TGGAAGTTTATACGC[A/T]ACAAGACATACACAA | 84669 |
rs568247303 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245632 | TGGACTTCACAAGGG[G/T]TCTGAGGGCAGCTAT | 84669 |
rs568258108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60205795 | CAGTATAAATAATTC[C/T]AGATTTATTGGAAGA | 84669 |
rs568266015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214088 | CTGGGACTACAGGCT[C/T]CCACCGCCATGCCCA | 84669 |
rs568270279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60205197 | ACATTAGCCACCATG[A/G]GTAATACTAAATCCT | 84669 |
rs568271544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60348287 | AATTAAAACCATGAG[A/G]AAGAAGCATAATGAG | 84669 |
rs568278930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60340883 | GTGACAAAATCTCTC[A/G]CCATTTGCTTGTCTG | 84669 |
rs568288230 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60307035 | AAGAAATTGAAGAGG[-/AC]ACACACACACAAAAT | 84669 |
rs568296374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332309 | TATATACCAATCACT[A/G]AACACAATGAAGAAA | 84669 |
rs568330450 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60213049 | TGAGCCACTGCGCCC[A/G]GCCTATTCATTTTAA | 84669 |
rs568333015 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60287391 | CATGTATTGATTTAC[A/G]ATTTTTGCCTGTAGC | 84669 |
rs568340546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60323238 | AAAAGTGGAAATAAC[C/T]CAAATATTCATTAAC | 84669 |
rs568345583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60191598 | CACTGCAAGCTCCGC[A/C]TCCCGGGTTCAAGCA | 84669 |
rs568352266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183580 | ATTTACTCTTCATTA[C/T]TTTTTAAAGACTTCA | 84669 |
rs568367201 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60182917 | AGGCACTGTGTGAAG[G/T]GCTTTACTCTCCATG | 84669 |
rs568376534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223721 | AGATTCTGGTAATTC[C/T]GTAGAAGACAGGAAA | 84669 |
rs568376962 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60331340 | GGAGGCCAAGGCAGG[C/T]GGACTGCTTGAGTCC | 84669 |
rs568412475 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60250761 | GTTCAAGACCAGCCT[C/G]GGCAATACAGTGAGA | 84669 |
rs568415577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289648 | TCATATGGTTGTTCA[C/T]GCCAATCCCTTTGCT | 84669 |
rs568420415 | in-del | -/TGT | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60258298 | AATTAAGAGAAAAAC[-/TGT]TGTCAGTTTGAGGAT | 84669 |
rs568449394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404385 | TTTTTTAATGTGATG[C/T]ACATGGAAGAGGTCC | 84669 |
rs568470294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347804 | TTCAAGGATTATGTT[A/G]TTATGTAGACAGAGA | 84669 |
rs568475762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258566 | CCTGATGGAGATTAA[G/T]ATGCCTTGAATTGTA | 84669 |
rs568481154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298346 | AGCCTGTCAAAATGG[A/C]CAACTTGCAGGCTAT | 84669 |
rs568500242 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420499 | ATGGAGAAACCCCGT[C/T]TTTACTAAAAATACA | 84669 |
rs568516729 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60186973 | TTTGTGTCCCAAAGC[-/A]AGAGCCCAGACCACA | 84669 |
rs568534440 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60315852 | CTGTACAAAACAGAT[C/T]GCCTGCAAACTGACC | 84669 |
rs568555640 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60297591 | GTAGCTGGGATTACA[A/G]TCACACGCCCAGCTA | 84669 |
rs568605333 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60372678 | GACCCCGTTCTCTAC[A/G]TTAAAAAAAAAAAAA | 84669 |
rs568614384 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411336 | TCAAAAATAAATAAA[C/T]AAATAAATAAATAAA | 84669 |
rs568618093 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420209 | ATGTTGGCCAGGCTG[C/G]TCTCAAACTCCTGAT | 84669 |
rs568641906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60381131 | AGCACTAGGTAGTCC[C/T]ATTTATTACGTCAAC | 84669 |
rs568651722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221264 | CTGTTATGGTGGTGT[A/G]TGCCTGCAGTCTTAG | 84669 |
rs568652713 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419297 | ATGTTCTCACTTATA[A/G]GTAGGAGCTAAATGA | 84669 |
rs568659773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60314026 | ATATGCTCAAGAATT[A/T]AAACAAAAATAAAAA | 84669 |
rs568665951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257806 | TTGGTGTTTTTTTTT[A/T]CCTTCAATCTGCTAT | 84669 |
rs568673675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60398333 | CCTGAAAAGTAGAGC[C/T]ACAGTTACCCATGAC | 84669 |
rs568686499 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60220706 | TGGAGTGCAGTGGCC[C/T]GATCTCGGCTCACCG | 84669 |
rs568687114 | in-del | -/AAAT | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60365484 | AGACTCCATCTCAAA[-/AAAT]AAATAAATAAATAAA | 84669 |
rs568716705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60397334 | TCATCTTGTGGATGA[A/G]AGATTTAAACTCAAT | 84669 |
rs568726785 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60351777 | CAAGATGAGTAATAC[A/G]TAGTCTCCATATTCT | 84669 |
rs568754764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60380626 | TTAGCCCACTTAATG[C/T]TTATTGTAGAGAAGT | 84669 |
rs568760549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60273169 | GTAGAGATGGAGTTT[C/T]GCCGTATCACCCAGG | 84669 |
rs568774674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60272485 | ACATTTATTCTCAAC[A/T]AAACACAGGAACCAA | 84669 |
rs568790961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60389125 | TTGTCAAATCCTATC[C/T]ACCCTTTCCCCCATT | 84669 |
rs568796213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60266694 | GGAGTCTCACTCTGT[A/C]GCCCAGGCTGTGGTG | 84669 |
rs568823766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373698 | TCAAATGATCCACCC[A/G]CCTCGTCCTCCCACA | 84669 |
rs568852283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404170 | AAATGATGGAATGTA[A/G]CAGAAGTGATACTGT | 84669 |
rs568887020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221867 | CAATGTAAAAAGTGA[C/G]TGTCCAGAGTACCGA | 84669 |
rs568889895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390131 | CACTGTATAAGAAAT[C/T]AAACAAAAACCTTCC | 84669 |
rs568894674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60241494 | AATCTTTGTCTCTTT[C/T]TTCAGAGTTCCAACA | 84669 |
rs568894864 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60184012 | TACCCGTCAGCCGGG[C/T]GCAGTGGCTCACGCC | 84669 |
rs568894922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60250563 | AATCCTACGTTAATA[C/T]ATTTTAAAATCTTTT | 84669 |
rs568896518 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60228429 | ATATCAAGCTTCTCA[C/T]AGCTTTTCTAATATG | 84669 |
rs568931192 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60187846 | TTACTTATAGGCACC[C/T]TCTTCTTTTTCAAAG | 84669 |
rs568931764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266165 | TTTTACTAGAAGTTG[C/T]CCTTGTATAATTACT | 84669 |
rs568932576 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60182795 | AAATAAAATAAATTA[A/T]AAAAAAAAGAGTTTT | 84669 |
rs568943744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183459 | GGTGAATAATCTGGA[C/G]AAGTAAAGGTAGAAA | 84669 |
rs568957448 | snp | A/G/T | 0.000709129 | 0.0188189 | intron-variant | USP32 | GRCh38.p7 | 17:60249691 | TTGTTCTCACCAAGG[A/G/T]TTAGTAGTTCTTGAA | 84669 |
rs568957822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60364445 | AGTGCGGTGGCGCGA[C/T]GTCCACTCACCGCAA | 84669 |
rs568958614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60291602 | AACACAAAGCATTGT[C/T]ATTGAAGGTCTGAAT | 84669 |
rs568962504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234933 | AATAATATCAAATGC[C/T]AGAGTGGAGAAGGGA | 84669 |
rs568964362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228994 | AAAAGAAAATTTTCC[A/G]TAAACATAAATGCCT | 84669 |
rs568989730 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60352370 | CAAAGTTATAAGCCA[C/T]ACAGTAAGGATGGCG | 84669 |
rs568994515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363523 | ACTCTGTCTCAAAAA[A/G]AAAAAAATTTGAGAC | 84669 |
rs569021412 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60309550 | GATGTTGCAGTGGGC[A/C]AAGACTGCACTACTG | 84669 |
rs569025119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60371728 | GACTGACAATATGAA[A/G]CACCAGTCCTGCAAG | 84669 |
rs569056740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60217161 | GCCACTTACTATACA[C/T]ACTTTTGTGCTTTTG | 84669 |
rs569061463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60370713 | GCTACAGTGAGTTGT[C/G]ATCACACCACTATAC | 84669 |
rs569062777 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60359544 | AGCAGGACACAGTGG[C/T]TCAAACCTGTAATTC | 84669 |
rs569067046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356647 | CACTAAGCAAATAAA[G/T]AATAGCAGGAACAAC | 84669 |
rs569079366 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418838 | CACACCAGTCAGAAT[A/G]ATGATGATTAAAAAG | 84669 |
rs569080078 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60316687 | CTCTACTAAAAATAC[-/A]AAAATGAGTCGGGTG | 84669 |
rs569101775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298245 | GTTGAATATGTACAA[C/G]TGGCCAACCTCTTCA | 84669 |
rs569104223 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60220469 | ATGACTTAAACAAAA[A/C]ATTTGGATGTAAAAA | 84669 |
rs569108654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339271 | AGTATGTCTAATGAG[A/T]TATGCACATAAGTGC | 84669 |
rs569124762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60219895 | TGTCCAACAAGTTCA[C/G]TAGCTACATTTCAGT | 84669 |
rs569143215 | in-del | -/T | 0.261332 | 0.249743 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418397 | CGTGCCTGGCCTCTG[-/T]TTTTTTTTTTTTTTT | 84669 |
rs569159958 | snp | C/T | 0.000183574 | 0.00957878 | intron-variant | USP32 | GRCh38.p7 | 17:60190524 | GGTGGAAATTTCTCA[C/T]ATAAAAACCACCATT | 84669 |
rs569176386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288961 | CAATAAGCCAGATTT[C/T]GTTTGCTAAGTATAT | 84669 |
rs569192183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60205759 | CAGTGTAGTCTCTTA[A/G]CACAGGGCAGGGAGA | 84669 |
rs569214514 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60249097 | AAGCTTGGCCTTCTT[-/G]GGGGTGAGCCTAACT | 84669 |
rs569220727 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60213111 | CTTGATGGGAAAAGA[C/T]ACACTTAAAAAGTTT | 84669 |
rs569220981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60198170 | TGATTAACTTGACAT[A/T]GGCTGGGTCCTATCA | 84669 |
rs569235915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197347 | TGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 84669 |
rs569278154 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60258531 | TTTAACAGCGTGACA[A/G]AAGTGACTTTGTTGT | 84669 |
rs569281935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60355718 | GCACACGCCTGTAGT[C/T]TCAACTACTCAGGAG | 84669 |
rs569285870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212926 | ACCCAGCTAATTTTT[G/T]TATTTTTAGCAGAGA | 84669 |
rs569286109 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418516 | AAGTGACTAATGGGA[C/T]CTAATTAAACTAAAG | 84669 |
rs569287113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60238215 | ACATGTATTCAAGTC[A/C]ATTTTTAGGTGTCTA | 84669 |
rs569293790 | in-del | -/AA | 0.00676609 | 0.0577691 | intron-variant | USP32 | GRCh38.p7 | 17:60385839 | TAGAGACTCTGTCTC[-/AA]AAAAAAAAAAAGAAA | 84669 |
rs569295113 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60246865 | TATTCAGATCACTTG[C/T]CCATTTTTAAATTGG | 84669 |
rs569304282 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP32 | GRCh38.p7 | 17:60380516 | GAGGCTGCAGTGAGC[A/G]GTAAATGTGCCACTG | 84669 |
rs569318430 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60288745 | CTTACTTGGAACCTG[C/T]ACAACCTGAAATTTG | 84669 |
rs569331161 | in-del | -/AG | 0.00398564 | 0.0444627 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408218 | GGACCCAGAAATGAC[-/AG]AAATTATGGAATTAG | 84669 |
rs569332458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60321832 | TGGTCAACTCTATTA[A/T]TCATTAACACCTCAG | 84669 |
rs569334198 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60205970 | TTTTCTTTTCCTTCT[C/G]TTTGCCTTTGAAGAC | 84669 |
rs569353279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257217 | GGCAATAATTTTATT[A/T]AAAAAGCCTTATAGG | 84669 |
rs569356105 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60258214 | AAAAACATGAAATGA[C/T]GCAAATGATAAATGA | 84669 |
rs569357600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360741 | GATGATAATGTGAAA[A/G]AAATGTGGTTGTTGT | 84669 |
rs569359700 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60245853 | CCTTCTTTTTTTTTT[A/G]ATGTGTTTTTTTTTA | 84669 |
rs569369348 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60204210 | ACAAAAAAACCAACC[C/T]CAAAACAAAAAACTT | 84669 |
rs569400327 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60254882 | TTTTAAAAAGACAAT[A/C]ATGAAGAAACTAGCA | 84669 |
rs569415343 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60351000 | ATCTGGAGTGGTCAC[A/T]GACCTAAGCCAACCC | 84669 |
rs569416981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60313761 | CACCATTACAAAGCT[G/T]TAACACAGGATTAAA | 84669 |
rs569430046 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60367300 | GGTTGCTTGAACTCA[C/G]GAGTTCAAGACAGCT | 84669 |
rs569453871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60312987 | GGTGGCTCATGCCTG[G/T]AATCCCAGATCCCAG | 84669 |
rs569460761 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60237963 | AGAATTGCTGGTACA[C/T]GGAAATTCTTGCTGA | 84669 |
rs569467172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60366981 | GGAGCCCGCCACCAC[A/G]CCCAGCTAATTTTGT | 84669 |
rs569505526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60293672 | CCAGAGTGGTAAGAA[A/G]CTAATGATAGGCAGT | 84669 |
rs569523249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60379633 | TAACACATAGAGAAC[C/T]TCTGTGTAGTGCAGT | 84669 |
rs569532745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216438 | TATCAATATAATGTA[C/T]ATTCCAAATAATTTT | 84669 |
rs569554695 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60285806 | GATTTAACACGTAGA[A/T]GAAAAAGAGAAGGCA | 84669 |
rs569560476 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407660 | GGTGGTCCATGCCTG[C/T]AATCCCAGCTACTCA | 84669 |
rs569562884 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60316368 | TGGGAAAATGGGGAA[C/T]GGAAATCAGGTATAG | 84669 |
rs569564178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387686 | ACAATGAGATTACCT[A/C]CCAATAAACCCATCA | 84669 |
rs569564290 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60286918 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACTTGA | 84669 |
rs569575753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60334526 | TGAAACCTCGTCTCT[A/C]CTAAAAATACAAAAA | 84669 |
rs569597360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60351894 | TGGAGTTCCAAAATA[C/G]GGAATAATTAGGAAG | 84669 |
rs569606578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408038 | GGGAGGTGGAGATTG[C/T]AGTGAGCTGAGATGT | 84669 |
rs569632664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194246 | ACAGTATTTCACCAT[C/G]TTGTCCAGCCTGGTC | 84669 |
rs569640537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302774 | AAGATACTCTCTAAC[C/T]GAATGTTCAGAAATT | 84669 |
rs569645732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222920 | CTCCTAACCTCAGGT[A/G]ATCTGCCCACCTCAG | 84669 |
rs569645919 | in-del | -/CTAT | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60361699 | CCTATCCTGTATAGC[-/CTAT]CTAAGGGTAGCTGTT | 84669 |
rs569701384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60209107 | CAATTACGGGGACTC[C/T]TTAAATTCCACTGGA | 84669 |
rs569746608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333480 | TGGCATGCTCCTGTA[A/G]TCCCAGCTACTTGGG | 84669 |
rs569757155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60262153 | CTAAAGCAAATTCAC[C/T]GACTATATGGCTTAT | 84669 |
rs569771009 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317070 | ATTGCTTAACAGGTA[C/G/T]AGTATTTCTGTTTGG | 84669 |
rs569775914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60310019 | ACTGCACTCCAGCCT[A/G]GGTGACAGAGCAAGA | 84669 |
rs569784938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60261474 | TAACATGGCAAAACC[C/T]GTCTCTACTAAAAAT | 84669 |
rs569789369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60341127 | TCATTTCAACCTTAG[C/T]GAATCTGACAACTAT | 84669 |
rs569798041 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305197 | TGGCTCACGGTTCTG[C/T]AGCCTGTATAAGCAT | 84669 |
rs569801822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60184523 | GAATAGAATAAGAAA[A/C]CATGGCTGGGCACGG | 84669 |
rs569809197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326278 | CTAGTAACCTGATTT[C/T]GGGTCCTTATTTGAC | 84669 |
rs569816895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423610 | ATGGGATTACAGGCA[C/T]GTGCCACCACACTTA | 84669 |
rs569845735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375688 | GGCTCACTGCAACCT[C/T]CGCCTCCTGGGTTCA | 84669 |
rs569852297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423061 | GATCTTCCTTGTTCT[C/G]CCCGAACACAGACTA | 84669 |
rs569865255 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60381908 | TCAGAGGTCACCACT[A/G]TTCTGTCACCATAAA | 84669 |
rs569871332 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60300200 | TGTGTAATATAAACA[G/T]CTGCCATACTTCCCC | 84669 |
rs569880428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384277 | CATCACCAAAAGGCA[A/C]CCATAGCAAATGTTA | 84669 |
rs569899232 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60268457 | ACATGCCTGTAGTCC[A/C]AGCTACCTAGGAGGC | 84669 |
rs569914470 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230621 | AACAAACTAGACTGG[C/T]CTGTCTTCTCATTGT | 84669 |
rs569923901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60384741 | AGGTTGCAGTGAGCC[A/G]AGACTGTGCCATTGC | 84669 |
rs569953346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60283463 | GTCCTTCATCCTTTC[A/G]TATCATTGAGAGGAA | 84669 |
rs569964144 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60267863 | TCTCCCAGGCTGGAG[G/T]GCAATGGCGCAATCT | 84669 |
rs569971601 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60176905 | TTCACAATAGGGTTC[A/G]TTCTCCTGTGAGAAT | 84669 |
rs569974772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60276171 | ATTGCTTAAGTCTAG[A/G]GGTTTAGGACCAGCT | 84669 |
rs569990519 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60375629 | TTGTTTTTGTGATGG[A/G]GTCTCGCTCTGTCGC | 84669 |
rs569994985 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392600 | AATCTTAGGGAATGG[A/G]GTTCTGAGGGATGCG | 84669 |
rs570000131 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60281276 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 84669 |
rs570003802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60284576 | GATACTACTAAAAAT[C/T]CAAAAAAAGATGATT | 84669 |
rs570019766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236601 | GGAATAATTTACATA[G/T]ATATAAAACTTACCT | 84669 |
rs570025366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60230788 | TCAGTGAAATAGCTA[C/T]CTTTTCATCCGATTA | 84669 |
rs570034076 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60392027 | GTCCCTGGGTGACGG[C/T]GACGGTGTCGGCGTC | 84669 |
rs570035075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60284010 | ATAAGAAGAATATTA[C/G]GAAACTACAATGTTT | 84669 |
rs570044710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308855 | ATTGCTCTAAACCCA[A/G]GAGGCGGAGGTTGCA | 84669 |
rs570062895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60349274 | AACTACTTGGTAATA[C/T]GTTTTTTAAAAATAT | 84669 |
rs570063416 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, stop-gained, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421462 | CCCACCGCACTGTCG[C/T]GAAGGCAGGCGAAGA | 84669 |
rs570068037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400084 | ATTTTCCCATCTCAG[C/T]CTCCTGAGTAGCTGG | 84669 |
rs570068481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60341956 | TGTTGCTGGCGAGGA[A/G]CTGCGATCCTTTGGA | 84669 |
rs570069851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60391310 | TCGTTCTTATCAAAG[G/T]CAGCCGCTCAAACGG | 84669 |
rs570079396 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60278437 | GTCTCGATGTTTAAA[C/G]AGGTACATGAAGAGA | 84669 |
rs570107851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60350558 | CCTCCCAAATTGCTG[A/G]GATTACAAGCATGGG | 84669 |
rs570136921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60244733 | GCCTCCTGGGTTCAA[A/G]TGATTCTCCCACCTC | 84669 |
rs570161579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60367122 | GTGAGCCACCGCGCC[C/T]AGCCTAAGCCCACTT | 84669 |
rs570162394 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60310730 | GTCATTTGCAGCAAC[A/G]TGTTAAGTGAAATAA | 84669 |
rs570170925 | snp | C/T | 0 | 0 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406584 | GCAATGGCATGACCT[C/T]GGCTCACTGTAATCT | 84669 |
rs570171543 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60261349 | AAATAAAGGCTGTTT[A/G]AAAAGTACAAATGTA | 84669 |
rs570172373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60359176 | TCCATGCCCCACCAC[A/C]TAAAATGTTAGGTGT | 84669 |
rs570197018 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60199958 | CCCAGCACTTCAGGA[C/G]GCCGAGGCGGGCGGA | 84669 |
rs570201830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60358377 | GTCAGGAGTTCGAGG[C/T]CAGCCTGGCCAACAT | 84669 |
rs570257412 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60206414 | CACGTGACTGGTGGA[C/T]ACTGTATTGGATGGC | 84669 |
rs570267905 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60228842 | TTTGTTTTTGTTTTT[G/T]TTTTTGGTAGAAATG | 84669 |
rs570291407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60260479 | AGTGAGCCAAAATCA[C/T]GCTATTACACTCCAG | 84669 |
rs570294099 | snp | A/G | 0.000181865 | 0.00953411 | missense | USP32 | GRCh38.p7 | 17:60207056 | GCTGAAATTGGAGAC[A/G]CAGGGACAGGAATTT | 84669 |
rs570304976 | snp | A/G | | | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414038 | TAGGATGTGGGTCCG[A/G]GTTTCTGAAAAACAA | 84669 |
rs570307813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222907 | GGCTGGTCTCAAACT[C/G]CTAACCTCAGGTGAT | 84669 |
rs570310847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60252750 | TCAGAATAATTCTTC[G/T]GACACTTGCATATGC | 84669 |
rs570313045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60357791 | TTTTTTTTTTGAGAC[A/G]GAGTTTCACTCTTGT | 84669 |
rs570314479 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60379469 | CAAAAGTTTAGCTTA[C/T]CTCTGCCAGGATCAC | 84669 |
rs570319838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222704 | TTTTTTTTTTTGAGA[C/T]GGGGTCTTGTTCCGT | 84669 |
rs570323169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60252037 | AATTATCTATAAATT[A/G]TCTATAAAATCTTTC | 84669 |
rs570324888 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60185029 | GTGTACACACACTCA[A/G]CTCAGTAGTGTGCCA | 84669 |
rs570334681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244875 | GGCTTCAAGAGATCC[A/G]CCTGCCTTGGCCTCC | 84669 |
rs570344910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60374451 | CCAGGCTGGAAGAGT[A/G]CACTGGCGTGATCAA | 84669 |
rs570372925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60316229 | CTTAAGAATATGCTA[C/T]GATGAGTAACATTTC | 84669 |
rs570376998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412267 | CCAGCACTTTGGGAG[A/G]CCAAGACAGAGAAGA | 84669 |
rs570383834 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60365424 | AGGTGAAGGTTGCAG[A/T]GAGCCAAGATCAGGC | 84669 |
rs570401354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60359602 | GATCACTTGAGCCCA[C/G]GAGTTTGAGACCAGC | 84669 |
rs570404750 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60422435 | ATGGGAGCGGGGTGG[C/G]GGGCTGGGTTCTGTG | 84669 |
rs570418051 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60229981 | ACTGCGCCTGGCTAA[-/T]TTTTGTATTTCTGGT | 84669 |
rs570424490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200664 | ACACTCAAAAGCCTC[C/T]CATTTGCTTCCTCCA | 84669 |
rs570443900 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422944 | TGTTGGAGGAGTTGA[C/T]CAGCCAGAGTCCTGT | 84669 |
rs570452311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60208910 | AAGAAGCTAGTTAAA[C/T]ATATTGGATTTAAAT | 84669 |
rs570455511 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60352111 | GCAGACAAAACAGAA[C/G]CCTGACTTTATTCAA | 84669 |
rs570466888 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60309373 | GGGAGGCTGACACAG[A/G]CGGATAACTTGAGCT | 84669 |
rs570490048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60207944 | TTGTTGTTCAGTTTT[C/T]GTTATGTTTTAGTAT | 84669 |
rs570491293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60344681 | GCTGGCCTGGAACTC[C/T]TGAGCTCAAGTGATC | 84669 |
rs570494610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229203 | CATCACCATGCCCAA[C/T]TAATTTTTAAAGTTT | 84669 |
rs570534230 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60238736 | TTGAACCCAGGAGGC[A/T]GAGTTTGCAGTGAGT | 84669 |
rs570539114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60340118 | CTCCATAGGATTTTG[A/G]AAAAGAACTCACAAG | 84669 |
rs570558277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216384 | TCTTCTCTGCTGAGG[C/T]TGTATTTTATTGAGC | 84669 |
rs570572858 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60325436 | ATACAAAAAAAAGAG[A/G]AAAAGAAAGAAAACT | 84669 |
rs570578069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384198 | CATGGGAAAGACTAG[C/T]GGAGGCCTATCTTGT | 84669 |
rs570590845 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60276564 | TAGCAGTCTTGACGA[C/T]AGAAACTGTTCTTAT | 84669 |
rs570606184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60326242 | ATAAATCAAAGATTG[A/C]ATTTCATCACACCCT | 84669 |
rs570610584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333247 | TTGATAACACATATT[A/G]TATGCCTTCCACAGT | 84669 |
rs570629813 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60222819 | CCCGAGTATCTGGGA[C/T]TACAGGCACACGTCA | 84669 |
rs570638765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333752 | AGGAAAGGAAAGAAA[A/G]TCGTAAAGAAGAGAA | 84669 |
rs570654489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60275364 | CAGGAGGCTGAGGCA[A/G]AAGAATCGCTTGAAC | 84669 |
rs570655710 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283671 | GGAAGAACAAGTTTG[C/T]CTTTTTTTTTTTTTA | 84669 |
rs570707875 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231156 | ATTCCCTGTGAGTTG[C/T]ATAAATAGTTTATGT | 84669 |
rs570717483 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60312760 | ATGTCACCAACCTAC[A/C]TGCTTAAAAGCCATC | 84669 |
rs570719714 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60281955 | GTAACTATCAATATG[C/T]CATAGTAGACTTACG | 84669 |
rs570727295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183716 | GGTACTGCCTCCAGG[A/C]TCAGTTGCTCTTCTA | 84669 |
rs570730343 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60205937 | CATGTTGTAGCACAC[A/G]AACAGTTCTACCACT | 84669 |
rs570731866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60184244 | GGCATGAACCCAGGA[A/G]GTGAGGCTTGCAGTG | 84669 |
rs570759268 | in-del | -/TTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60280090 | GGTAAATTGAGTAAG[-/TTA]TTATTATTATTATTA | 84669 |
rs570769559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60283920 | AGAACAAACTAGAGC[A/G]AAGGGCTGATCCACT | 84669 |
rs570776407 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60253288 | CTGAATATGTTCGTG[C/T]ACAAACAGCATATGA | 84669 |
rs570795451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192184 | TAGTCCCGGCTACTC[A/G]GGAGGCTGAGGCAGG | 84669 |
rs570802684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235852 | TCACAAGGGTGGTGC[A/G]AGAAATAAATGAGAT | 84669 |
rs570807830 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60249350 | TCTCCTGAGTTTGTG[C/T]ATAGCCTTGTACAAG | 84669 |
rs570826666 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60399235 | AAAGTAAAAGCTCCT[G/T]CTCTCATGGAATTTA | 84669 |
rs570830298 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60398690 | GCTTAGCTAGGTACA[G/T]TGGCTGGCTCAGAAA | 84669 |
rs570848030 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60324302 | TATATATATATATAT[A/T]TTTTAATTAAAAACT | 84669 |
rs570862912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405854 | GCATAGAATTTTATT[C/G]TTTCAAAGGTTATTA | 84669 |
rs570863027 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60262388 | GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG | 84669 |
rs570866541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243773 | GTCTATCCTAGAACA[A/C]TACTCTGTCTACATT | 84669 |
rs570889139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60358246 | ATAACATTGTTTCTA[C/T]GGAAAAATAAGTTTT | 84669 |
rs570902654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60225909 | CAGTGAGCAGAGATC[A/G]CGCCACTGCGCTCCA | 84669 |
rs570945601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60345677 | TCATAATTTTTTTCA[A/G]CCTGGCTCCTAAGAA | 84669 |
rs570975764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60251911 | TATGATCTAGAGTGA[A/G]AATAGGAGCAGGGAA | 84669 |
rs570982167 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60344840 | AAACTTTTATTTTAT[C/T]TTTTTTAGAGACAGT | 84669 |
rs571000251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405272 | CAGTGGCTCAATCTC[A/G]GCTCACCACAGCTTC | 84669 |
rs571002398 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60328999 | GGTAGTGTGAGCCTG[C/T]CAGGCCAAGTGGATG | 84669 |
rs571028056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306562 | AGAATCACTTGAACC[C/T]GGAAGGCAGAGGTTA | 84669 |
rs571036580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412169 | ACCGGTATTTTCCAA[A/T]TTTGCCCGATGATGA | 84669 |
rs571048538 | snp | A/C/T | 0.000418676 | 0.0144626 | missense | USP32 | GRCh38.p7 | 17:60214663 | TCTTCCTCTTTAATG[A/C/T]GCAGCCTTTGAGATA | 84669 |
rs571068221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60195116 | GAGCTACCATGCCTG[G/T]CTATCTTTTTTAATG | 84669 |
rs571077950 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419374 | ACCAGAGAGTGGAGG[A/G]TGGGAGAAGTGAGAG | 84669 |
rs571083853 | in-del | -/CCTTCTCTGTG | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60375181 | TTTATGAAGCTCCCT[-/CCTTCTCTGTG]GATACCACGCTTCTT | 84669 |
rs571086790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60250959 | CTTTTCTTTTTTTTT[A/T]TTTGAGAGAGTCTCA | 84669 |
rs571095524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214177 | AAACTCCTGACCTCT[A/G]GTGCTCCAGCCACCT | 84669 |
rs571102067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60364643 | TGCCTCCCAAAGTGC[C/T]GGGATTATGGGCGAG | 84669 |
rs571113391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60311844 | CAAAACAAAAAAAAA[C/T]GGTAGATATGTGTAG | 84669 |
rs571123713 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60382184 | CCTTGCCAGATCCTT[A/T]TCTGTCAAAACTAAG | 84669 |
rs571126446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288113 | AGGGAGACTTCGTCT[C/G]AAAAAAAAAAAAAAA | 84669 |
rs571131017 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60202258 | CTCTATTCTATCCCA[A/G]TGGTCTACTTGTCTT | 84669 |
rs571148823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60233921 | ACTCCTCTCCTCCCA[A/G]GTTTATTGTAACTCT | 84669 |
rs571152177 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60258645 | TTTCTTTTCCTTTTT[A/T]AAAAATTAAACAGAT | 84669 |
rs571155087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347646 | GCGTGAGCCACCGCG[A/C]CCGGCCTACACCTGG | 84669 |
rs571162342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60240417 | TTGACAGTGATTTCC[C/T]AGAATGGCAGAAGTG | 84669 |
rs571187431 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60372989 | GGCTAACATAGCGAG[G/T]TCTCTACAAAACATA | 84669 |
rs571199537 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60179865 | TTAGTAAAGGCGGGG[A/T]TTCACCATATTAGCC | 84669 |
rs571223924 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60384829 | AATAAAGAGCCTGGC[C/T]GGGCGTGGTGGCTCA | 84669 |
rs571227994 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233257 | AATCGCTTGAGCCCA[G/T]GAGTTCGAGACTAGC | 84669 |
rs571228923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60354300 | CATCTCTATTTCTTT[A/T]AGACAGCCAAGGCAG | 84669 |
rs571268480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60394571 | TATGACCGCATGTGT[C/T]GTTTTCCAATGGGGT | 84669 |
rs571281679 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60187304 | CTAAAGAGCTCATTT[-/A]AAAAAGGGGAACTTA | 84669 |
rs571285544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60298109 | CCCAAAGTAAACATC[A/G]GGCCTAACTGTAATG | 84669 |
rs571286174 | snp | C/G | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419559 | AACACAGTGAAACCC[C/G]GTCTCTACTAGAAAT | 84669 |
rs571291213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60239827 | CAACCTCCGCCTCCC[A/G]GGTTCAAGGGATTCT | 84669 |
rs571404809 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402351 | GACCTCCCAGGCTCA[A/C]GTGATTCTCCCACCT | 84669 |
rs571405529 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415908 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT | 84669 |
rs571409969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263455 | CGAATATGGTTAATA[C/G]GCTTGGTTAAAAAAC | 84669 |
rs571413355 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60365776 | TTGTATGTAATTTTA[C/T]TAAAATACCAAAAAT | 84669 |
rs571416759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60286698 | GAAGATGTTTGATTT[C/T]CCTATAGCAACTAAA | 84669 |
rs571418635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60277354 | ATTTTCATACAGTAA[C/T]ACATTTCTTTAACAT | 84669 |
rs571437923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360913 | GCAGGCAGATCGCTT[G/T]AAGTCAGGAGTTCGA | 84669 |
rs571441674 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60349992 | AGTTCTGCTCTGTGG[-/T]TTTTTCGTTGTTGTT | 84669 |
rs571448254 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60396002 | ATGGACTTGTTACCT[G/T]ACAGTCAAACAATAT | 84669 |
rs571449067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60247771 | TCATTGCAACCTCCA[C/T]CTCCCCAGTTCAAGC | 84669 |
rs571475609 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP32 | GRCh38.p7 | 17:60401301 | CGTGAACCAGGGAGG[C/T]GGAGCTTGCAGTGAG | 84669 |
rs571480102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60285839 | TTAGTGATAGAAAGA[A/C]GCATAAGAAAAAGCA | 84669 |
rs571512332 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60247340 | GCCTGCCACCATACC[C/G]AACTAGTTTTTGTAC | 84669 |
rs571512810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256221 | CTCCAAATCAGAATA[C/G]AGAAATAAGCTAAAG | 84669 |
rs571516761 | snp | C/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423224 | TGAGACAGAGTCTCA[C/T]TCTGTCACCTAGGCT | 84669 |
rs571522963 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60255401 | CTCCTGGGTGCAAGC[A/G]ATTCTCCTGCCTCAG | 84669 |
rs571578398 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378270 | CCATTAGGATGGTTA[G/T]TAATTGAAAGAAAAC | 84669 |
rs571605075 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178735 | AATAAATTGAAAAAT[C/T]CTCGTCCATGCCTTA | 84669 |
rs571624673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254493 | ACTACTTGAGCCTAG[A/G]AGTTTAATACCAGCC | 84669 |
rs571645905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60372599 | AATCCCAGCACTTTG[A/G]AAGACTGAGGTGGGA | 84669 |
rs571649250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407631 | ACAATGTGACATCCA[C/T]ATTAGCCAGGTGTGG | 84669 |
rs571677999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60224642 | TAAAAAATTAGCTGT[A/G]TGTGGCAGTGTACAC | 84669 |
rs571681482 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60385186 | GCTCAGAAGCTCCCC[C/G]ACTGGGCACCTCGTG | 84669 |
rs571711795 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409020 | AGACACAGCTGAGCA[C/T]TTCCTCCTATTTCCT | 84669 |
rs571712708 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392950 | GCTTAGCGTGGAGTC[A/G]TTTTAATCTGTGGTA | 84669 |
rs571721350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60335449 | GGTCCAAGGTCTCTA[C/T]GTGATTTTCAATTCT | 84669 |
rs571738421 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60334611 | GCAGGAGAATGGCCT[G/T]AACCCGGGAGGCGGA | 84669 |
rs571739740 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393655 | ATTCTAATATACCCT[G/T]CTAGAGAAAGAAGGT | 84669 |
rs571741007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223873 | GTCCTCCGACTGGAA[C/G]GGAAGAGCTGGGCTA | 84669 |
rs571748141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60374277 | TTCCACCTTCACGTA[C/T]TGTCCCACTGGAAAG | 84669 |
rs571753943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231840 | AGATTACACATAGAA[A/G]AATAAAGCTTGACAC | 84669 |
rs571767978 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60238376 | CTTGATGTATAAAAG[G/T]TTTAAGTTTTGCCAG | 84669 |
rs571784785 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60186075 | AGGGAAAAGAAAACA[C/T]AACCCAAACTAGAGT | 84669 |
rs571787451 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60289229 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG | 84669 |
rs571810793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60351951 | ACCTGGCAAAAAAAA[A/C]CGCAAAGGGCTATTC | 84669 |
rs571832352 | snp | C/T | 9.91457e-05 | 0.0070401 | missense | USP32 | GRCh38.p7 | 17:60185614 | GGCTCGGCTTGCGCT[C/T]GCCGACTCTGCTCCA | 84669 |
rs571854122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60238052 | TATGAGAGTCCCTAA[C/T]TTCCCTACTTGCCAA | 84669 |
rs571884059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60262869 | ATTATTAAAGTGCCA[C/T]ATCCCAGCAGAAATC | 84669 |
rs571895909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60342896 | GGGTGAGGCAACGCC[C/T]CACCCTGCTTCACCT | 84669 |
rs571917982 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393910 | GCTGTTCTCGAACTC[A/G]CAACCTCAGATGATC | 84669 |
rs571935715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302006 | TACTCCATAAATTAC[A/G]TAAGATATTTAACAC | 84669 |
rs571940164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60335980 | AGACTCACTTGGATA[A/G]GATCCCAACTGTTTT | 84669 |
rs571949529 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60351345 | GGACTACAGGCATGC[A/G]CCACTATGTCAGGCC | 84669 |
rs571953196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194175 | CAGCCTCCCAAGTAG[C/G]TAGGATTACAGGCAC | 84669 |
rs571969720 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422178 | TTCCTCTCGGGGAGC[C/T]CCCACCACGGCGTAA | 84669 |
rs571981533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60350958 | AGAACCTAAGAGACA[A/G]TCAAATTTTTCTGGT | 84669 |
rs571984920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194215 | TACCTGGCTAATTTT[C/T]ACATTTTTTGTAAAG | 84669 |
rs572008573 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60291707 | GCAGGCAAATAAATC[A/G]AATAGTTGAATCAAA | 84669 |
rs572009948 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393087 | GTTTTTCATCTTGCA[A/G]AAGGGAAACTCTGTG | 84669 |
rs572016325 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60234161 | CTCTGTCGCCCAGGC[C/T]GGAGTGCAGTGACGC | 84669 |
rs572018574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60193118 | TACACTCTGGCTTCC[C/T]ATCCTCTATCTGGGC | 84669 |
rs572031259 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60398190 | GGCAACATACGGAGA[C/T]TCTGTCTCTACAAAA | 84669 |
rs572038021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60334686 | AACAAAGCGAGACTC[C/T]GTCTCAAAAAAAAAG | 84669 |
rs572043332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60200173 | CACTCCAGCCTGGCC[A/G]ACAACAGCAAGACTC | 84669 |
rs572045638 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60294572 | TAAATATAAAAATGC[C/G]AAGAGTAATCTGCAC | 84669 |
rs572051367 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178274 | TGCATGTGTTCTCTC[C/T]TTTTTAAAGTGCAAG | 84669 |
rs572062946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60246036 | GGGTTGGGAATATTC[C/T]GAATCTTCTAGCTAA | 84669 |
rs572104195 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60208334 | CCTAGAATTTTTATT[A/T]TATGTGTAAACACTA | 84669 |
rs572110258 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60302156 | ATTTATTTATTTGAG[A/T]TGGAGTTTTGCTCCT | 84669 |
rs572112841 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60384279 | TCACCAAAAGGCAAC[C/T]ATAGCAAATGTTAAA | 84669 |
rs572117422 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60323035 | GAAATTGGAACCCAC[A/G]TATACTATTGGTAGA | 84669 |
rs572125936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400380 | GGGCGACTGCATTAA[C/T]CCAGGCGTGAGGGTT | 84669 |
rs572127842 | in-del | -/CAGAGGTTGCAGTGAGCCAAGATCGCACCACTGCATTCCAGCCTGGGTGA | 0.084728 | 0.187577 | intron-variant | USP32 | GRCh38.p7 | 17:60313182 | CTTGAACCTGGGAGG[lengthTooLong]CAGAGTGAGACTCTG | 84669 |
rs572139214 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177300 | ACACCCCATATACAA[C/T]TACCAATACTTTTTA | 84669 |
rs572149775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185786 | AATACAACTGGCTGG[A/G]TATGGTGGCTCATGC | 84669 |
rs572158862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325694 | CACTTTTGGAAGTTG[A/G]GGCTGGCAGATCGCT | 84669 |
rs572220652 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60285447 | GTAGTCAAGTTATAT[A/G]TCATATAAAGTAATG | 84669 |
rs572220714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60293724 | ATACATGCAAAGGCT[A/G]AAATATGGACAATCA | 84669 |
rs572248140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407708 | AATTGCTTGAACCCA[A/G]GAGGCGGAGGTTACA | 84669 |
rs572273835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60184780 | ACACCACTGCACTAC[A/G]GCCTGGGTGACACAG | 84669 |
rs572295981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254138 | AAATAAAATAAGAAG[A/T]AACTAAAATAACCAC | 84669 |
rs572311573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60366315 | AGACACATGCCACCA[C/G]GCCCAGCTAATTTTT | 84669 |
rs572325845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236013 | CATTTCCTTTCCCTT[C/T]GAATCTTTATTTAAG | 84669 |
rs572326089 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308727 | GAGGTCAGGAGTTCA[A/G/T]GACCAGCCTGGCCAA | 84669 |
rs572328451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60367017 | TAGTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 84669 |
rs572342834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60309495 | TAATCACAGTTACTC[A/G]GGAGGCTGAGGTGGG | 84669 |
rs572347940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60216612 | TAAAAAGTCACCTAA[A/G]AAACAATGACTTCTA | 84669 |
rs572350206 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60199382 | ATTTGCTTTGAGTAC[A/G]TTAAAGAGATATTTA | 84669 |
rs572365754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375862 | ATCTGCCTGTCTCAG[A/C]CTCCCAAAGTGCTCG | 84669 |
rs572385061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183989 | ACCTCAATTTTTTTT[A/T]AAAGGTCTACCCGTC | 84669 |
rs572418682 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373491 | CTTTGACACCCAGGC[C/T]AGAGTGCAGTGGCAC | 84669 |
rs572431579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60291110 | AGGTTAAGGAATTTG[C/T]CTACTGTTATACAGT | 84669 |
rs572440046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60260843 | AGTAGTCAGAATAGT[A/C]TATCTTCCCCTCTAA | 84669 |
rs572444892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375192 | CCCTCCTTCTCTGTG[A/G]ATACCACGCTTCTTC | 84669 |
rs572446275 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60274108 | CTAAGGAAAGAAATG[A/G]CAACTATAAAGAAGT | 84669 |
rs572499220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60275094 | GTATGTTTTGTTCCC[G/T]GTTACAGTCTAACAC | 84669 |
rs572504971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60204554 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 84669 |
rs572521489 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | USP32 | GRCh38.p7 | 17:60313231 | ATTCCAGCCTGGGTG[A/G]CAGAGTGAGACTCTG | 84669 |
rs572523297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60322198 | TAAGGTTATTTTAAG[A/G]TGAGTTCTTGCCATG | 84669 |
rs572534294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222341 | TTAGTGAGAGTCACA[C/T]AGAAAAAGTAACAGA | 84669 |
rs572548399 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60273909 | AGGCTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 84669 |
rs572550529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267499 | TAATGTACATTCAAT[A/C]TTTTTTTGGCAAAAA | 84669 |
rs572553307 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60335565 | TGAATGGTGAAGTAG[A/G]AAAAAATATATCTAC | 84669 |
rs572558228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60321130 | TGAGGAGAGGAAGAA[A/G]CTCAGGAAAGTTGTC | 84669 |
rs572560511 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60303836 | TCAACAGAGTTGCAT[A/G]AGAGATTATCCAAAA | 84669 |
rs572571849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60384333 | TGCTGGGGCAACCAA[A/G]CTTCTTTACAGAAAT | 84669 |
rs572574114 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60391314 | TCTTATCAAAGTCAG[-/C]CGCTCAAACGGTGAA | 84669 |
rs572594218 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60188655 | TAATAACTTTTTGCT[A/G]TTCTAAAAAATGCTA | 84669 |
rs572607108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60383385 | AGCTCTCCACAACTT[C/T]TCTCCATTATTTATA | 84669 |
rs572608687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60399559 | TCCCAGATGCTTGGG[A/G]GGCTGAGATGGGAGG | 84669 |
rs572623359 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60300679 | TTTAAAAAATAAGTT[A/C]TATTGAGACATAATT | 84669 |
rs572624053 | in-del | -/GGATT | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232442 | CCTCCCAAAGAGCTG[-/GGATT]GCAGGTGTGAGCCAT | 84669 |
rs572626378 | in-del | -/T | 0.0970103 | 0.197722 | intron-variant | USP32 | GRCh38.p7 | 17:60346115 | AGAAAATAAGTATAA[-/T]TTTTTTTTTTTTAAG | 84669 |
rs572673249 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60280698 | CTACTTATAAATCAG[A/T]TAATAACATTCCCTA | 84669 |
rs572689757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60390619 | ATCTCAATTCTGTAT[C/T]TTACTGTCAGGTGAT | 84669 |
rs572695627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60398870 | CCTTCGGTCCCAGCT[A/G]CTTGGGAGGCTAAAC | 84669 |
rs572714726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60243458 | AAGCCTTCAGTGTTC[C/T]ACCATTAAGTATGAT | 84669 |
rs572742778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60349440 | CAAAAATTAGCCAGC[C/T]GTGGCGGTGGGTGCC | 84669 |
rs572745496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405980 | AAACATAGTTAGACG[C/T]CACCTCTCCAAAATG | 84669 |
rs572757382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60212624 | CTTATCCCTCAATTA[C/T]CTACTTGAAGTAAAA | 84669 |
rs572770205 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60251889 | AATATATTAAAGTAT[G/T]ATTTTATATGATCTA | 84669 |
rs572776178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305698 | TGGCATCCCTTTCCA[G/T]TCACTGTATCTTGAT | 84669 |
rs572783585 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60180087 | CTGGAGTGCAGTGGC[A/G]CAGTCTTGGCTCACT | 84669 |
rs572787730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60288331 | TGTAGTCCCAGCTGC[C/T]TGGGAGGATGAGGTG | 84669 |
rs572790723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60213124 | GATACACTTAAAAAG[C/T]TTTTAATGGCATGTG | 84669 |
rs572796770 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60286717 | ATAGCAACTAAAGAT[A/C]ACATCTTAATATGTG | 84669 |
rs572798340 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60219254 | AATTGCTTTTTACAA[A/G]TTTGAGTGGAGTTGA | 84669 |
rs572821311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60220073 | AAACCCTAAGTATTA[C/T]CTATAATTCTACTAC | 84669 |
rs572822848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418062 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 84669 |
rs572827719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60371960 | ACTTACTACCTAATT[C/T]CAGCTGTGAATCCTA | 84669 |
rs572851011 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60287872 | TAATTCCAGCACTTC[A/G]GGAGGCCGAGGCGTG | 84669 |
rs572881428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402575 | TTATTCTTCTGAAAC[A/G]CTAAATTAGTAATCA | 84669 |
rs572909566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60257302 | CGGCATGCACAGTTA[C/T]TTCTTCATGTTACTT | 84669 |
rs572912779 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60352884 | CTGAACAGGGTTCAC[G/T]GAATAATTAGCTGTC | 84669 |
rs572946272 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60329554 | CCTCAAGCATTCCTC[C/G]CACTTCAGCCTCCCA | 84669 |
rs572957229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408656 | GTGCTGGGATTACAG[A/G]CATGAGCCACCATGC | 84669 |
rs572962386 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60371305 | GGCGCAGTGGCTCAC[A/C]CGTATAATCCCAGCA | 84669 |
rs572964200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60380690 | AATTATATAAATTAC[A/G]TGGGAGAAAAAAAGC | 84669 |
rs572972313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264511 | CAGAGCAAGATCCTG[C/T]CTCCAAAAAAACAAA | 84669 |
rs572980099 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378674 | ACATTATCCTAAGTG[-/A]AATAAGAAAGGTCAA | 84669 |
rs572991099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256560 | ATCTGTGTGGAGTTT[G/T]CATATTCTTTCCATG | 84669 |
rs573008868 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60284327 | CAAGTGATTCTCCTG[C/T]CTCTGCCTCCCAAGT | 84669 |
rs573033550 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60312038 | GGCCTGACATTGAAG[C/G]CAGGCTTTATTAATA | 84669 |
rs573056778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60337357 | GTTTCCTCTAATCTA[C/G]AAAAAGGTTAAGTGT | 84669 |
rs573071657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60239960 | CAGGCTGGTCTCGAA[C/T]TCCTGACCTCAAATT | 84669 |
rs573075289 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60383555 | ACAAACTGTTCAGAA[C/T]ATTGCACAATAGTGA | 84669 |
rs573077318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280079 | CTAAAATCTTGGGTA[A/T]ATTGAGTAAGTTATT | 84669 |
rs573092994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416090 | TGATCTGCCCGCGTC[A/G]GCCTCCCAAAGTGCT | 84669 |
rs573116470 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60323660 | AACACTATTTCTTTT[A/G]AAGCAAAGAACTGGT | 84669 |
rs573118976 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60184750 | GAGAGGTGGAGGTTG[C/T]GGTGAGCTGAGATTA | 84669 |
rs573132696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233520 | ACTCATTTAATCCTC[A/G]TAACACTATGAGGGC | 84669 |
rs573175340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60344965 | AGTGGCGCCGGTTAA[A/G]CATATTATTTTTAGA | 84669 |
rs573179809 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60262381 | ATTTTTAGTAGAGAC[A/C]GGGTTTCGCCATGTT | 84669 |
rs573186019 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60350015 | TGTTGTTGGTTTTTG[-/T]TTTTTTTTTTTATTT | 84669 |
rs573186817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60247905 | TAGCCAGTATGGTCT[C/T]AACCTCCTGACGTCA | 84669 |
rs573188097 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60200102 | GGGAGGCTGAGGCAG[C/G]AGAATCACTTGAACG | 84669 |
rs573200232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378048 | AATCATATATCTGAT[A/G]TGAGAATAATATCCA | 84669 |
rs573219742 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60239580 | ATTCATTCTTCTGCC[C/T]GCTCATATCTGATGG | 84669 |
rs573225115 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60218337 | TGCAGTGAGCCGAGA[C/T]CGTGCCACTCCACTT | 84669 |
rs573240291 | in-del | -/T | 0.0869089 | 0.189476 | intron-variant | USP32 | GRCh38.p7 | 17:60369293 | CCACCGCGCCCGGCC[-/T]AAAAGATATTTTTTA | 84669 |
rs573265048 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60357476 | AAAAATAAATATATA[C/T]ATGATATGTAGACCA | 84669 |
rs573278307 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360788 | TAAATTAGTTTTTCA[C/T]TACACAAGCAGTAAG | 84669 |
rs573280227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60369469 | TTTTACTACACTCCA[A/G]GATAAATTTTGGGTG | 84669 |
rs573292683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211935 | TTGAACTAGAAAACC[A/G]AAAGTTGTTAGCACT | 84669 |
rs573303290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60219200 | AAACCAAACAACAAC[A/G]AAAACCTTAAAAAAC | 84669 |
rs573312374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60353822 | AGAACTCACTGTCCA[C/T]GAAAGGAAAATAAAA | 84669 |
rs573332723 | snp | C/G | 0.193653 | 0.243567 | intron-variant | USP32 | GRCh38.p7 | 17:60334647 | CAGTGAGCCGAGATC[C/G]CGCCACTGCACTCCA | 84669 |
rs573348366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60368657 | CTACCCATCAAAAAA[C/T]AGTAAACATAAAGTA | 84669 |
rs573367679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60218329 | GCGGAGCTTGCAGTG[A/T]GCCGAGATCGTGCCA | 84669 |
rs573404683 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60180025 | TTGCATTAACTAACT[C/T]CTGTTTTTTTTTTTT | 84669 |
rs573436755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60269816 | ATCTTACATCATTTT[A/T]AATGGCTAAAATGAC | 84669 |
rs573457096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60217858 | TCTTCCCACCTCAGC[C/T]TCTTGAGTAGCTGAG | 84669 |
rs573468939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210800 | CATCCCGAATTTAGA[A/G]TGTACCTTTGGTCTT | 84669 |
rs573517507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60379887 | CAATCATCAAGCATA[C/T]GCTAAATTTGTGCTT | 84669 |
rs573519572 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60389831 | ACCATCCCGGCTAAC[A/G]CGGTGAAACCCCGTC | 84669 |
rs573522140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60268964 | TAATGGAATGTATTT[A/G]TGCTTACAAATTATG | 84669 |
rs573523643 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60357490 | ATATGATATGTAGAC[C/G]AAGCAAGCAACAGAG | 84669 |
rs573527958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327666 | GGCAGTGAGCGAAAG[C/G]CCCGCCCTCTCAGAT | 84669 |
rs573528933 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60336273 | CTGTTTAAATTTGCT[A/C]TAGCTTAAAACTTGA | 84669 |
rs573529815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60318393 | TAATCTAATTCCATC[C/T]AGAGAACAGCATGGG | 84669 |
rs573572295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60219971 | TTAAAATTCCTGCTC[C/T]GAAACCCATTTCCTA | 84669 |
rs573580638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60312435 | GTTGTTGTCGTTGTC[A/G]TTGTTGTTGAGACAG | 84669 |
rs573590957 | in-del | -/A/AA | 0.283421 | 0.247756 | intron-variant | USP32 | GRCh38.p7 | 17:60336715 | GCGAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA | 84669 |
rs573591039 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182318 | TTCCCGTATTAGAAA[C/T]TAAAACTAAGGAATG | 84669 |
rs573626532 | in-del | -/TA | 0.00878763 | 0.0657008 | intron-variant | USP32 | GRCh38.p7 | 17:60323275 | ATAAACAAAATGTTA[-/TA]TATATATATGCATAC | 84669 |
rs573644014 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60259295 | AAAGAGAAGAAGTCA[C/T]TATTTTTCACTGAGC | 84669 |
rs573674602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417357 | CTCTATGTTGCCCAT[G/T]CTGGTCTCTAACTCC | 84669 |
rs573705760 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60317409 | TAGTACCAGCGACTC[A/G]GGAGGCTGAGCTGGG | 84669 |
rs573720465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302438 | AGGCATGAGCCACCG[C/T]GCCTGGCCTGAGCAC | 84669 |
rs573730203 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233410 | GGCTGTAGTGAGCTA[A/T]GATTGTGCCACTACA | 84669 |
rs573755552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424179 | AAGGATCCACCCCCA[C/T]GACCCAAACACCTCC | 84669 |
rs573755599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415221 | GGAGGGCTGGATGTA[C/G]GCTGCTGGCAGGGAA | 84669 |
rs573760794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60270990 | TACTGGAGGAAGAGA[C/T]GAGGTCATGTGTGGA | 84669 |
rs573766059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225309 | AAAACACACAAAAAA[C/T]GGCTGGGCATGGTGG | 84669 |
rs573766622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402393 | GTAGCTGGGACCACA[A/G]GCACACACCACCACA | 84669 |
rs573773884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387799 | TAGAACACTTACATT[A/G]GCATACTGTTGGACA | 84669 |
rs573794496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60287003 | AAATACAAAAAATTT[A/G]GCTGCACATGGTGGC | 84669 |
rs573797397 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242496 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGCTCAA | 84669 |
rs573806706 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256262 | AAAAACAAAAACTCA[-/T]TTTTGTTTTTTCAAA | 84669 |
rs573829342 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232654 | TAGGTTCGAGCTATT[C/T]TTGTGTCTCAGCCTC | 84669 |
rs573846452 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60344415 | TTACAGGTGTGAGAC[A/C]CCTTGCCCAGCCATA | 84669 |
rs573856302 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60353118 | TTTGGAGTAAGGAAG[A/C]AATTATTGTTAAATA | 84669 |
rs573883357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60352993 | ATGAAGATTAGTCTA[A/G]GGGAGAATTTGAATA | 84669 |
rs573891720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423349 | AGGTATGCATTACCA[C/T]ACCTGGCTAATTTTT | 84669 |
rs573894320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60195281 | ACTCCTTTCCTGAAA[C/T]ACTTCCTTCACTTAA | 84669 |
rs573900608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409135 | CACGGATCACCTGAG[A/G]CCAGGACTTCAAGAC | 84669 |
rs573931842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60194556 | TGCAGCACCCAGTTC[A/G]CTGTGTTTTTTCTCC | 84669 |
rs573932473 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60239918 | TTTGTATATTTTTTA[G/T]TAGAGACGGGGTTTT | 84669 |
rs573966685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60353720 | CACCCCAGCCTGGGA[G/T]ACAGAGTGAGACTCT | 84669 |
rs573971534 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60268107 | TGAGCAACCATGCCC[A/G]GCCAACAATTTTAAC | 84669 |
rs573974444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60311263 | CAAAAAATGTATCTA[C/T]TATGCAACCCTAAAG | 84669 |
rs573978481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60255518 | TTGGCCAGGCTGGTC[G/T]TGAACTCCTGACCTC | 84669 |
rs574012713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60319186 | ATGGCTGCAAAATAT[C/T]GTGAATGTAGTTAGT | 84669 |
rs574012861 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393965 | CTGGGATTACAGGCG[G/T]GAGCCACCGCGCCCC | 84669 |
rs574021691 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418197 | TCCCGACCTCAGGTG[A/G]TCTGCCTGCCTCAGC | 84669 |
rs574033115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60368583 | CTAGTGAAAAACCAA[C/G]AATATTACCAAAAAA | 84669 |
rs574039731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60310378 | GATAAAGAAAATGTG[G/T]TATATACACACAATG | 84669 |
rs574041309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60262945 | CTCACCGTAATACTT[C/G]GTGCTAACCTTTTTT | 84669 |
rs574060371 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60324187 | CTTGGGAGGCTAAAG[C/T]GGGAAGATTGGTTGA | 84669 |
rs574068853 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60255020 | CAAACTTCAGCAAGC[A/C]CCCATCTTTCAGACG | 84669 |
rs574080959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60262333 | AGTAGCTGGAATTAC[A/T]GATGCCCAACACCAT | 84669 |
rs574083708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60299255 | TCTTAAAAATGATCT[A/C]TTTGTCCATTTTGTG | 84669 |
rs574095937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60298702 | TATATTTCTGCTGGT[A/G]AAGAAATGCTAATTT | 84669 |
rs574103505 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60363750 | GCAATCCTCCCACCT[C/T]AGCCTCCCAAAATGC | 84669 |
rs574108016 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | USP32 | GRCh38.p7 | 17:60246419 | TATATATATATTTTT[A/T]TTTTTTCTTTATCCA | 84669 |
rs574133238 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60377063 | AAAAGAAACCTTTTT[C/T]GGCCAATATTTACAT | 84669 |
rs574137954 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60360401 | CAGTGGCTCATGCCT[C/G]TAATCCCAGCACTTT | 84669 |
rs574146289 | snp | A/G | | | synonymous-codon | USP32 | GRCh38.p7 | 17:60301615 | TTTTGCTTTCTCTTC[A/G]TCTTTGCCTCTTGTA | 84669 |
rs574151821 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420706 | AAAAAAACCTCTTTC[C/T]TGACTGTAAAAGTAA | 84669 |
rs574184912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259555 | CTGAACTGGAATAAG[C/T]GGGTTGGAAATGAAT | 84669 |
rs574187426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60317647 | TAGCGAGACCCTCAC[C/T]GCTACAAAATATTCA | 84669 |
rs574194109 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60369906 | CATGCTCAGCTAATT[-/A]AAAAAAAAGATTTTG | 84669 |
rs574195470 | in-del | -/TTTTATTTT | 0.0019856 | 0.0314461 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420084 | GTTTATTTTATTTTA[-/TTTTATTTT]ATTTGTTTTGTTTTA | 84669 |
rs574199143 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60258901 | TTTTTTGACCTTTCC[A/C]TTCTTTAAAAATACA | 84669 |
rs574201504 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60367935 | TAACAGCCATTTACA[C/G/T]GGCACTTACACTGTA | 84669 |
rs574212551 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178136 | AAACAAAGCAAAACT[A/G]AAGTTGACTTCCTAA | 84669 |
rs574216617 | snp | A/G | 0.000328216 | 0.0128063 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231695 | AGTTACGTGATAACT[A/G]AATAGGAAAATCTGC | 84669 |
rs574241062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223191 | CAGAATAGCTGTCCT[A/G]AGTAAGAATAACAAT | 84669 |
rs574247853 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60376122 | ACAATCATGGCTCAC[A/T]ACAGCCTCAAATTTC | 84669 |
rs574271915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60385094 | GGTTCCTGCCTTAAC[C/T]GATGACATTCCACCA | 84669 |
rs574272728 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60217793 | CCCAGGCTGGAGTAT[G/T]GTGGCACAATCATAG | 84669 |
rs574283265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60384504 | ATAGTGATGAGCGCC[A/G]CCCTAGGCCAGGCAC | 84669 |
rs574285828 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419657 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 84669 |
rs574286901 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60217023 | TTGGAGCATCTGAAA[C/T]ATGCAGTTCTAGGAT | 84669 |
rs574319717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327015 | AAAGTTGGTTATGTA[C/T]AGAAAAGTACAGCCA | 84669 |
rs574323391 | in-del | -/AGTAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60397668 | ACCCCACTACCTATT[-/AGTAC]AGTGCTTCCATTCTG | 84669 |
rs574327443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60361418 | TAGTTTTTCATTATA[C/T]AACATTAGTAATATA | 84669 |
rs574329316 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60199348 | CAGGATAGGATAAAA[A/G]TAAGGTAAAATTTTT | 84669 |
rs574334823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405424 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGAGCTCA | 84669 |
rs574358315 | snp | A/C | 0.197082 | 0.244335 | intron-variant | USP32 | GRCh38.p7 | 17:60334670 | GCACTCCAGCCTGGG[A/C]AACAAAGCGAGACTC | 84669 |
rs574369665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60198628 | GTTACAGTGGAGTCA[C/T]TAAAGGGGCTGAGGT | 84669 |
rs574371980 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265593 | TGTAGAGATGGGGTC[C/T]CCTTACGTTGCCCAG | 84669 |
rs574387867 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60394560 | AATTAATAGAATATG[A/C]CCGCATGTGTCGTTT | 84669 |
rs574394230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60334190 | AGTATTATAATATAT[A/T]TTACAGTTAATTTTA | 84669 |
rs574401292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60252148 | TTTATCTCATTTCAA[A/C]AAATGAAATTTAGTA | 84669 |
rs574425444 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60340096 | GCTCTCCATAGGATT[A/T]TTTTTTCTCCATAGG | 84669 |
rs574428771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60389579 | AACTTTTTTTGTAAT[C/T]TTAAATTCTATATTA | 84669 |
rs574452514 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60365477 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAATAAAT | 84669 |
rs574467951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388642 | GCAATATAAACAAGA[A/G]TCAAGGCTTTCCTTG | 84669 |
rs574487862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60343463 | TGTCTCTGAGACCAC[A/G]GTGCAATCAAATTAG | 84669 |
rs574493744 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60256376 | TCTTATCATGATCAC[-/T]TTTCAAAAAATTGTC | 84669 |
rs574522906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315157 | AATCCTAGCACTTTG[A/G]GAGGCCGAGGTGGGC | 84669 |
rs574527742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60357878 | GGTTCAAGCAGTTCT[C/G]CTGCCTCAGCATCCC | 84669 |
rs574541611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234708 | GCACTCCAGCCTGGG[A/C]GACAAAAGCAAGACT | 84669 |
rs574543746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60241581 | TCTTAGAGCTACCCA[A/C]TACATAATTTTCACT | 84669 |
rs574552625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60328767 | GACGCCATCACACTC[C/T]CCGGGAGCAGCCAGA | 84669 |
rs574553801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60234289 | CGGCTAATTTGTTGT[A/G]TTTTCAGTAGAGACG | 84669 |
rs574591770 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60334769 | TGTATTCTGTGTATA[A/C]GTAGACCTGCGCTAT | 84669 |
rs574618139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60206190 | GGCATGGTGGTACAC[A/G]TTTGTAGTCCCAGCT | 84669 |
rs574649650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60228557 | GATGGTGGCTCATGT[C/T]TGTAATCCCTGCACT | 84669 |
rs574651739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60273854 | AGTCCCAGCTACTCC[A/G]GAGGCTGAGGCAGGA | 84669 |
rs574687410 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60233958 | GCCTTTATTTATTCA[C/T]TTATGTTATGAGACA | 84669 |
rs574694018 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60281489 | GTTGCAGTGAGCTGA[C/G]ATCATGCCACTGCAC | 84669 |
rs574728202 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177739 | TTCAATTTAGGTAGC[C/T]ATTTAAGATAACCTT | 84669 |
rs574728367 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60227842 | CTTCACTTTAGTAGC[A/C]AAAAAATTTTTTTAA | 84669 |
rs574729609 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377531 | AAAGATAGGAGGCAT[C/T]TCTCATTCTTATGGT | 84669 |
rs574733623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363570 | GCCAAGGCTGGAGTA[A/C]AGTAGTGCACTGTAG | 84669 |
rs574735308 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60374022 | AAACCCATCTCTACT[A/G]AAAATACAAAAATTA | 84669 |
rs574738113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60322638 | GGTTCAAAAAAAGGA[G/T]ATAGTCCCTGGGTTC | 84669 |
rs574752509 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60300884 | AGCAACCACTAATCT[A/G]TCATTTTCTGCCACT | 84669 |
rs574752745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60396480 | GAATGACTAAAAATA[C/T]GTCATTCTCTAATCT | 84669 |
rs574767556 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60339292 | ACATAAGTGCTAAAA[A/G]GTATAAATGGCCGAG | 84669 |
rs574769284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60338679 | AGGATGCAGTGAGCC[A/G]AAATTGCACCACTGC | 84669 |
rs574772519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60363164 | TTAAATTAAAAAAAA[A/T]TTTTTTGAGGCCAGG | 84669 |
rs574788790 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411216 | TGTAATCCCAGCTAT[C/T]TGGGGGCTGAGGCAG | 84669 |
rs574816850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60278790 | GACTTGGAGCTGCTA[A/G]ACTGCTTGGAGAGGA | 84669 |
rs574818606 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60282197 | TATTTAAAGCAAACT[A/G]ACTCTTCATGTGCCT | 84669 |
rs574819955 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60260276 | CTGTAATCCCAGCAC[C/T]TTGGGAGGCTGAGGC | 84669 |
rs574820608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60212439 | TATCTAAACATGTTA[A/G]AACATAGAAAAGGCA | 84669 |
rs574837312 | snp | A/G | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423802 | CCACTTTTGTGGTCA[A/G]AGGTTCTTTCTCATC | 84669 |
rs574843845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60197835 | GAAAAAAGAATGACA[C/T]GGTATGGAAATAATC | 84669 |
rs574854497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190188 | TTGCCTGTGTCTGTT[C/G]TCCTTTGATCTTCTC | 84669 |
rs574860568 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60193080 | TACTTACCCTAATCC[A/G]TTAGCTGCAGCCCAG | 84669 |
rs574875560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60331053 | TCTCAGAACTTAAGT[G/T]ACTAGGAAAAGATCA | 84669 |
rs574880273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403570 | TCCAGGGGGACTAAC[A/G]CTCCTCAGGTGTGGT | 84669 |
rs574882925 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60346003 | ATAAATAAATAAAAA[A/G]AAAAAAAAAGAAAAA | 84669 |
rs574888411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60196946 | AGTACTTTGAGAGGC[C/T]GAGGTAGGTGGATTA | 84669 |
rs574889193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249774 | ATGGTTGTTTGACAA[C/T]TTTGTTCAGTTTTTT | 84669 |
rs574901962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60289002 | GTAAACTGCATTTTG[C/T]TTTTTGTTTTTGTTT | 84669 |
rs574988696 | snp | A/T | | | synonymous-codon | USP32 | GRCh38.p7 | 17:60214632 | TACCTCACTGTTGTA[A/T]AGCCACAGGCGCATA | 84669 |
rs574996322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60313125 | TCATGGTGGCAGGCA[C/T]CTGTAATCCCAGCTA | 84669 |
rs575022625 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60311253 | ATGTACCCCCCAAAA[A/C]ATGTATCTATTATGC | 84669 |
rs575051472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60371020 | ATTGCTTGAGACCAG[A/G]AGGTTGAGACTATCT | 84669 |
rs575066957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60272894 | GTCTTACTGAGTTTT[C/G]GCAGAATAGTAAGCT | 84669 |
rs575078407 | snp | C/T | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60256706 | GGAAAGGAACATCAA[C/T]GCCTGCACCACGGCA | 84669 |
rs575103571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237623 | TTAACAACCACCAGT[C/T]TGCTGTCTGGACCTA | 84669 |
rs575105707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60203722 | GCTAGGACTACCGGC[A/G]TGTGCCACCATGCCT | 84669 |
rs575106636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418627 | ATCCTACAAAGGTCT[A/G]ATATCCAGCATCTGA | 84669 |
rs575130217 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP32 | GRCh38.p7 | 17:60206027 | AGATGTTGCATTTAA[A/G]ATTTAAATTAGGCTG | 84669 |
rs575132444 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60282339 | ATCATAATTCATTTC[C/G]CCCTAAAAACATAGT | 84669 |
rs575134382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356393 | CCAAAATTCCCATAT[C/T]TCTCACTTTGGCTGA | 84669 |
rs575139895 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60359453 | CTCTTGTCCAAGGCC[-/T]TATGCTTATTACTAA | 84669 |
rs575143573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418008 | TTGTTACCCAGGCTG[A/G]AGTGCAATGGCACGA | 84669 |
rs575144479 | snp | C/T | 3.3507e-05 | 0.00409297 | intron-variant | USP32 | GRCh38.p7 | 17:60205435 | CAGTGAGTTGCCTAA[C/T]ATTTAACTAACCATT | 84669 |
rs575169281 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60298054 | TCACCTTTTGACTTA[C/T]AGGGCCTAACTGTAA | 84669 |
rs575176827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60271873 | CTGGAGTGCAGTGAC[A/G]CGATCATAGTTCCCT | 84669 |
rs575176868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60281400 | AAAATTAGCCAGGCG[C/T]GGTAGCAGGCGCCTG | 84669 |
rs575191306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60396361 | GGATTATAGGTGTGA[C/G]CCACCACGCCTGTCC | 84669 |
rs575192252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60280860 | AGGTAATATAAATCA[C/T]AGTCATCAAATTGTA | 84669 |
rs575195334 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60357372 | GCAGGAGGACTGCTT[C/G]AGCCCAGGAGTTGGA | 84669 |
rs575209559 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60314235 | CAACCTCTGCCTCCC[A/G]GGCTCAAGCAATCGT | 84669 |
rs575214241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315119 | TAAAATGAATGAGGC[C/T]GGGTGTGGTGGCTCA | 84669 |
rs575220350 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410819 | GGTGCGGTGGCTCAC[C/G]CCTATAATCTCAGCA | 84669 |
rs575262902 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60268966 | ATGGAATGTATTTAT[A/G]CTTACAAATTATGCT | 84669 |
rs575274123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60213181 | TACAAATAGCTCTGT[A/C]AGTGAGTAGCCAATG | 84669 |
rs575292865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60249010 | GTAGAGTTTATCTTC[C/T]GGTACAGTATCTTGC | 84669 |
rs575314909 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60311594 | TTGGGAGGCCGAGGA[C/T]GGTGGATCACCTGAG | 84669 |
rs575329540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214217 | AAAGTGATGGGATTA[C/T]AGGCGTGAGCCACTG | 84669 |
rs575348308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60250213 | TTCCACTTTTACAAA[A/T]TGAGAGACACTAATT | 84669 |
rs575352265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60388540 | CAAACTTAGATGCAA[A/C]AAGGAGGTGAAATAA | 84669 |
rs575355815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60362967 | AGATTAATAATAAAT[A/G]TTGCATCTAATCCAG | 84669 |
rs575357621 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60248029 | CCATTGGTCTATTTG[G/T]CTGTTCTTATGTCAG | 84669 |
rs575378680 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60345889 | TGGGAGGCTGAGACA[C/T]GATAATCACTTGAAC | 84669 |
rs575380553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402626 | ATGCATTACTTTGCT[G/T]ACATGAGTATACCTG | 84669 |
rs575389884 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60348604 | ACATAGTGAGACCCT[-/G]TCTCTACAAAAACAG | 84669 |
rs575401736 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP32 | GRCh38.p7 | 17:60380098 | CAAAGAAGGTAAGAT[C/T]TAGGCAAAGTCCAGA | 84669 |
rs575428460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60321157 | TGTCTTTTGAACTCC[G/T]GGGTATACCTCCCAG | 84669 |
rs575441590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60372202 | ATACAAAGTGGTCTC[C/T]TCTAAGAGAAGGAAA | 84669 |
rs575465233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60329731 | ATTACCTACTTATAT[A/C]TGACAGACTGTCAGA | 84669 |
rs575470122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60256657 | ACAGGAGTGTCTAAA[C/T]TGTCCCACTGTAGTG | 84669 |
rs575503877 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60220832 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCAC | 84669 |
rs575508434 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60318618 | TGGCTTTTAGCTGCA[-/C]CCCCCACCTCCAAAC | 84669 |
rs575514395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60220200 | AACTATGGAAGTATT[C/T]ATTAGCTATATAGTC | 84669 |
rs575525139 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60247618 | TGTATGCTCTTGGCA[A/T]CTTTGTCAAAAAAGA | 84669 |
rs575528884 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60234244 | TCACCCTCCCGAGTA[C/G]CTGGGACCATAGGCG | 84669 |
rs575542661 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60330904 | TCACCCTTCTCCCCT[C/T]CATTCCAGGCAAGTT | 84669 |
rs575556822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60180425 | TGACAGCATCTATAT[A/C]TTGATTCTAACAGAA | 84669 |
rs575583685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60338601 | TGGGCGTGGTGACAC[A/G]CACCTGTATTCCCAG | 84669 |
rs575598410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60345953 | TGCCGCCGCACTCCA[A/G]CATGGACAACAGAGC | 84669 |
rs575601339 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392316 | CGCCCAGGGCCGCAC[G/T]CTCCGCCCCTCCCCA | 84669 |
rs575611853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60287885 | TCGGGAGGCCGAGGC[A/G]TGTGGATCACGAGGT | 84669 |
rs575613995 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227582 | TCAGTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTG | 84669 |
rs575654497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60240062 | TTTCCTTTAGTTTGT[C/T]GTCCATCACCTCCAT | 84669 |
rs575670676 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60237525 | GTGACCACCTCTTAT[A/T]AAGTTTCAAAACATT | 84669 |
rs575671485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60189309 | TTTTGGGATCTAAAT[A/G]AGAAACTAGGTCTAG | 84669 |
rs575680664 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60386774 | ATTTTGCTCATCCCC[C/T]AAAATCCAGAGTTCA | 84669 |
rs575683269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60236986 | TTTTGTTTATCCATC[A/C]AACACCTAAAGAACA | 84669 |
rs575702567 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP32 | GRCh38.p7 | 17:60203687 | GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCCTG | 84669 |
rs575713678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60354048 | AGAAATCACATGCAT[A/G]TGTGAAATGCATGAA | 84669 |
rs575735207 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60369075 | TCTCGGCTCACTGCA[A/G]GCTCCGCCTCCCGGG | 84669 |
rs575753148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60359765 | GCAGTGACCTATGAT[C/T]GAACCACTATACTCC | 84669 |
rs575765925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60211745 | AATTATTCTTTTTAA[C/T]TGCTATGATTTTTCA | 84669 |
rs575771435 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP32 | GRCh38.p7 | 17:60326467 | AGGCACCGACAACCA[C/T]GCTCGGCTAATTTTT | 84669 |
rs575779582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409334 | GCCTATGCAACAGAG[C/T]GAGACTCCGTCTCAA | 84669 |
rs575782305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60399855 | GCCAGCAAGGAAGCA[A/G]GTGTGCCTGCAACAG | 84669 |
rs575788699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60358877 | GGATGTCACTTGCCA[A/G]GATTGAGAATCTCTG | 84669 |
rs575789479 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60302997 | AATAATTCGAGAAGT[C/T]AGTCAATATGAAAAC | 84669 |
rs575789907 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60383645 | TGTGGCCATCAGATA[-/T]GAGAATGAGCCAGAC | 84669 |
rs575802300 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178140 | AAAGCAAAACTAAAG[C/T]TGACTTCCTAAAACC | 84669 |
rs575804904 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232708 | TACACCACCATACCC[A/G]GCTAATTTTTGTATT | 84669 |
rs575806141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60320486 | AGACATCCACACTCA[C/T]TCAGACTGGGACAAC | 84669 |
rs575810548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60202770 | CTCTAAAACAGTATA[C/T]CCATATATCCATGTT | 84669 |
rs575818663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417158 | CCTGACCTCAGGTGA[A/T]CCACCCACCTCAGCC | 84669 |
rs575840979 | in-del | -/AAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60284122 | TGAAACTAAAAAGAA[-/AAC]AATCATTAGGAATTA | 84669 |
rs575848697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263902 | TTTATTTATTCTAAA[A/C]CTCTATTTAATAACA | 84669 |
rs575877528 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378690 | AATAAGAAAGGTCAA[A/C]TATTGTACGATTCTA | 84669 |
rs575879348 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60251316 | CCGTTTTTAAAACTT[C/G]TCATTTAAAAACTTA | 84669 |
rs575905922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60263235 | TTATAGATGAGAACT[A/G]CCATGCCCAGCCTCA | 84669 |
rs575922186 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60211193 | CGCAAAAATGCCTAG[C/G]ATCTCACATCAAAAT | 84669 |
rs575922847 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60263175 | CTGGTCGAGAGCTCC[C/T]GGGCTCAAGTGATTC | 84669 |
rs575948672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60285146 | GATATTAACAGAAAA[C/G]TAATTTACCATACAA | 84669 |
rs575954236 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306570 | TTGAACCCGGAAGGC[-/AG]AGGTTACAATGAGCC | 84669 |
rs575961892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60215633 | AAGTAGCTCAATTAT[C/T]TGGCACAGTGGTACA | 84669 |
rs575965714 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230946 | AAACATCAAAGGATC[A/T]TGTTTTGTTTTTATT | 84669 |
rs575966392 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60284277 | GGAGTGTAGTGGCAT[C/G]ATCTTGGCTCACTGC | 84669 |
rs576004829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60292882 | ACTCACGCTGTCCTA[C/T]AGGACAATATATAAT | 84669 |
rs576030154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222246 | TATGAATGAATGAAC[A/G]AATGTGAAGGAACTT | 84669 |
rs576069967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60351019 | CTAAGCCAACCCAAG[A/G]AAGTTAAAACCTAGC | 84669 |
rs576075908 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60350138 | CCACCTCAGCCTCCC[A/T]AGTAGGTGGGACCAC | 84669 |
rs576091934 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60221673 | CACCACACTGGATAA[G/T]TTTTGTATTTTTATT | 84669 |
rs576093840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200836 | TTATATTTATAAATA[G/T]AATTACTTAATTCAT | 84669 |
rs576102555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332540 | GTGATCCCAGCTACT[C/T]GGGAAGCTGAAGCAG | 84669 |
rs576128991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183842 | GCAGTTCTCACATCA[C/G]ACTGAATTGCAGTTA | 84669 |
rs576137464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407112 | TTGCCTAGGGGTGCA[A/G]TCTGGATCATAAAAT | 84669 |
rs576142939 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406264 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 84669 |
rs576167501 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60194718 | AGACCTTGTGAATAC[A/C]AACTTTTCTACCTCC | 84669 |
rs576171653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414201 | AACCTCATCTCTACT[A/G]AAAATACAAAAATTA | 84669 |
rs576175408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60199569 | AGTAGTTAGAAAAGC[G/T]AAATCAACAACTTAT | 84669 |
rs576181359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413442 | TGCTAGGCTAAGTCA[C/T]AAACCAGTACAGGGA | 84669 |
rs576183363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60185129 | GGTTAGCCTAAGCTT[C/T]CTCTCTCCACAGAGC | 84669 |
rs576198567 | snp | A/C | 1.72219e-05 | 0.00293439 | intron-variant | USP32 | GRCh38.p7 | 17:60208225 | ACTAGTAAAGAGAAA[A/C]GATCTTTTATTGGTA | 84669 |
rs576221207 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60325424 | CCTGTCTCAAAATAC[-/A]AAAAAAAAGAGAAAA | 84669 |
rs576222175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60253289 | TGAATATGTTCGTGT[A/G]CAAACAGCATATGAA | 84669 |
rs576244985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60316370 | GGAAAATGGGGAACG[A/G]AAATCAGGTATAGGG | 84669 |
rs576245221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192520 | GCTCACTGGAACCGC[C/T]GCCTCCTGGGTTCAA | 84669 |
rs576246445 | snp | A/G | 3.38146e-05 | 0.00411171 | missense | USP32 | GRCh38.p7 | 17:60252405 | TGTCCTTCTTCTTCC[A/G]GAGTAGCTGGTCTTA | 84669 |
rs576249788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60301431 | CTGTAATTTTAATTT[A/G]TATTTCTCTAATGAC | 84669 |
rs576260607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60259872 | TTCAAAGCTTAATAT[C/T]AGAAGTGCTTGGGGT | 84669 |
rs576274473 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60339515 | TTGAAACTGGGAGGC[A/G]GAGTTTGCAGTGAGC | 84669 |
rs576277815 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60299287 | TGCTATAATAAAATA[C/T]CACAGATCTAGCAAC | 84669 |
rs576289492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60207246 | CATCCGTAAAACCAA[C/T]GAGATGATTGAATAA | 84669 |
rs576306776 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60335945 | TTATAATACCTATTA[A/T]GGATAGAAGTTTCTC | 84669 |
rs576315937 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373960 | GAGGCCGAGGTGGGC[A/C/G]TATCACCTGAGGTCA | 84669 |
rs576316389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60375045 | ATGAGATCATTAGTG[A/G]AATTTTCTCCCTTTA | 84669 |
rs576326247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308635 | TAACTATACGCAGAA[A/G]AATAAAACTAGGCTG | 84669 |
rs576343962 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60362632 | TCATTAGTTTTTTTC[A/G]TTTCCATAATATAAC | 84669 |
rs576356559 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60316054 | TGATATGGGACTTCA[A/C]AACAGATCTGTGCTT | 84669 |
rs576364944 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421958 | GAGGGTTACAGAGCC[C/T]GTAGGCACTGGCGGG | 84669 |
rs576379900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325582 | AAGAAAGTTAAATAC[G/T]TATCTCTTCTACAAA | 84669 |
rs576394818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325018 | CAAAAAAAACAAAAA[A/G]CTGTTGGAAGGTTTA | 84669 |
rs576413723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267465 | ACAGTCCACTTCCAT[A/G]TTACCTTTCCAGTAT | 84669 |
rs576416579 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60401707 | CCAACATGGTGAAAC[A/C]CCATCTCTATAAAAA | 84669 |
rs576429786 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366616 | ACATTTAGAACTAAA[A/T]TAAGCCAGGTGCTGT | 84669 |
rs576436207 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60241435 | TTTAAAAAATTATTA[-/T]TTTTTTTATAATTTT | 84669 |
rs576446306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60229331 | TACAGGCATGAGTCA[A/C]CCGGCCAAAGGCATT | 84669 |
rs576455801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60382369 | AGGTGTGGTGGTGCA[C/T]ACCTGTAGTCCCCAC | 84669 |
rs576464779 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60298548 | TTCTTATTTGTATTA[-/T]TTTTTTTTGCTGTAC | 84669 |
rs576471834 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242796 | GTATCCTTAGGTAAA[-/T]TGTGAAATCAGGAAG | 84669 |
rs576476172 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60203797 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAC | 84669 |
rs576477713 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60275528 | ACACATACCCCCACA[A/C/T]CCCTCTTCAGGATAA | 84669 |
rs576500681 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421155 | ATATAATTATCCTTC[C/T]TAATACTCGCAAAAT | 84669 |
rs576514259 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60207771 | GTAACAGCAGCAGTC[C/T]TTGGTGGAAACCTAT | 84669 |
rs576515408 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60272461 | TAAAATTTACAAAGC[A/G]TACATAGGACATTTA | 84669 |
rs576525244 | snp | A/G | 3.31642e-05 | 0.00407198 | missense | USP32 | GRCh38.p7 | 17:60183195 | TGATGTTAGCGCTGA[A/G]TGAGGATGGGCTTTT | 84669 |
rs576536002 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60290937 | TGCTATCTCCAGGTA[C/G/T]ACCCTTCTACCACCT | 84669 |
rs576537494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228753 | GGCCTCAACCCAGGG[G/T]GTGGAGGTTGAAGTG | 84669 |
rs576556750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235947 | AGGAAAGAAATGTAT[G/T]TGGAAGTGTAATCAC | 84669 |
rs576584319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60274995 | TCCATAATACTTATC[A/C]ACTCTAATATAAAAT | 84669 |
rs576599144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60235296 | TTTTCTACCTACACA[G/T]ACCATCATTATCTAC | 84669 |
rs576621210 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60348580 | AGGAGTTAGAGACCA[A/C]CCTAGGCAACATAGT | 84669 |
rs576643625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347997 | CCTGGTGGCGGGCAC[C/T]TGTAGTCCCAGCTAC | 84669 |
rs576644073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60390588 | GTTATTCTGGTAAAT[C/T]CACCACCACCAATAC | 84669 |
rs576660962 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60259667 | AGCCTCCCATATTTG[C/T]TATTGTTAGTTTTTG | 84669 |
rs576682020 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60304367 | TTATTTTTTTATTTT[A/T]TTTTTTTACGGAAAC | 84669 |
rs576682249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60389739 | AAATTCATGCCGGCC[C/G]GGCGCGGTGGCTCAT | 84669 |
rs576682407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60398802 | GGGCAACATTGCAAG[A/G]CCCTGTCTCTACAAA | 84669 |
rs576695676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60222127 | CTTTTTGGCACTGGC[C/T]CTTGGCCTGTCTTCC | 84669 |
rs576714190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60373886 | TAAAAAGTTTTTACT[A/G]TTCATGTTTTATTTT | 84669 |
rs576724735 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP32 | GRCh38.p7 | 17:60184038 | ACGCCTATAAACCCC[A/G]CGCTTTGGGAGGCCA | 84669 |
rs576755407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60382089 | ATTAGGGCCAGTGTA[C/T]GATTTCTATTTCCAG | 84669 |
rs576760748 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60329320 | TAAGAGTTCCAGAGG[G/T]GTCTTAGGATAGGAC | 84669 |
rs576770466 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60242848 | CATTTTTTTGAAGTT[C/G]TTTAGGCTAGTCTGA | 84669 |
rs576791717 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60381493 | CTATTTGCCTCCTAC[C/T]CCTCCAATTCATTCT | 84669 |
rs576810271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60221570 | AGTGCAATGGTGTGC[A/C]GTCTTGGCTCACTGC | 84669 |
rs576815849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60244165 | CTCAGCCTCCCGAGT[A/G]GCTGGGACTATAGGC | 84669 |
rs576827478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60279623 | AGGTAGATCACTAGA[A/G]CCCAGGAGTTTGAGG | 84669 |
rs576830572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60251055 | TCAAGCAATCCTCCC[A/G]CCTCAGCCTCCCAAG | 84669 |
rs576870075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60228639 | CCCGAGCAACGTGGA[C/T]AGATCCCGTCTTTAC | 84669 |
rs576884170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60227989 | GAATTTTGGACCATC[A/G]ATTTTTAAAATTTAG | 84669 |
rs576884858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60366137 | CATGTGACACCACGC[C/T]GGGCTAAGTTTTTTT | 84669 |
rs576884885 | in-del | -/TGC | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60221884 | GTCCAGAGTACCGAG[-/TGC]TGTTTACCGTGTAAG | 84669 |
rs576889783 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60357976 | TTTTCACCATGTTGG[G/T]CAGGCTGGTCTCGAA | 84669 |
rs576890918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60339435 | TAAAAATACAAAAAT[C/T]AGCCAGGCGTGGTGG | 84669 |
rs576898110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60299414 | TCCATCATCCCATAG[C/T]GGAAAGCAGAAGAGC | 84669 |
rs576924398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60365718 | GAAACAAAGTAATTA[C/T]TAAAAGAATGCATTA | 84669 |
rs576927485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60338855 | TATTTTATTCAAGTA[A/C]TACATGGTTACGATT | 84669 |
rs576927509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347849 | CAGGAAAGGCTGGGC[A/G]CAGTGGCTCACGCCT | 84669 |
rs576931983 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416494 | TATGGCACATATTTG[G/T]ATTAAAAAAAATGTG | 84669 |
rs576936607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60192001 | GAACTGGCAAACTTA[C/T]ATTTAACGAGAGGCT | 84669 |
rs576938639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60200026 | TGGTGAAACCCTGTC[A/T]CTACTAAAAACACAA | 84669 |
rs576944039 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | USP32 | GRCh38.p7 | 17:60234744 | TCAGAAAAAAAAAAA[A/T]TTTTTTTTGTTTTGT | 84669 |
rs576954190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412458 | GAAGATCACCTGAGT[C/T]TGAGAGGTCAAGGCT | 84669 |
rs576957353 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60421675 | TGCCGCGCCAGGGGC[A/G]AGGGTCCCGGGGCCT | 84669 |
rs576966853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60207227 | AGAATGTCTTAGGCG[C/T]TTTCATCCGTAAAAC | 84669 |
rs576975217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60214927 | AGTACCAAAACGCTT[C/T]AAAATGCAGGCAGGA | 84669 |
rs576991453 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421022 | GGACTAATTCCTCCT[A/G]TAAGTAGAATTGGTG | 84669 |
rs576998697 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60260913 | AAACAAAAAAAACCC[-/AGA]AGAACTGCAAGCTCT | 84669 |
rs577015660 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60225418 | GCCGTGATTATGCCA[C/T]TGTACTCCAGCCTGG | 84669 |
rs577033641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60214317 | ATAATCTTTGAAAGA[C/T]AGTACTGTCCATGGT | 84669 |
rs577043902 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60197726 | ATCAAATAGAACAGT[G/T]ATAGGAAAAAGGGAA | 84669 |
rs577052944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60308573 | ACAAAGAAAATACAA[C/T]GGGGGAAAGAACAGT | 84669 |
rs577062435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60347196 | AAGCTTTTTTTTTTC[A/T]TTTTTTGAGACAGAG | 84669 |
rs577080712 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60243525 | AGGAATTTCCCTTCC[C/T]CAAAGTTGTGAATGA | 84669 |
rs577114851 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60343340 | CCACCCCAAATCAAC[-/A]GAACATACATTCTTC | 84669 |
rs577120055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306483 | TCTCTACTAAAAATA[C/T]AAAAATTAGCTGGGC | 84669 |
rs577123120 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60206294 | TGCACTCCAGGCTGG[C/G]TGACAGAGTGAGACC | 84669 |
rs577127405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60315963 | CATCATTACAGGCCT[C/G]GTCTGGTACTCTGTG | 84669 |
rs577141877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60273916 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 84669 |
rs577154854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60196983 | GCCAGGAGTTCGAGA[C/G]CAGCCTGGCCAACAT | 84669 |
rs577160816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60332465 | CCAGCCTGGCCAACA[C/T]AGTGAAACCACGACT | 84669 |
rs577165536 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP32 | GRCh38.p7 | 17:60315192 | TGCCTGAGCTCAGGA[A/G]TTCAAAACCAGCCTG | 84669 |
rs577168546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60389672 | ATACAATTTTATCAA[C/T]TTGCTGCTCTCTTTT | 84669 |
rs577183891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378144 | GGGCAAAGGATTGAA[G/T]AGACATGTCTCCAAA | 84669 |
rs577196646 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP32 | GRCh38.p7 | 17:60331957 | ATTTAAAGTATACAA[G/T]TGAGGTCAGGCACAG | 84669 |
rs577208890 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP32 | GRCh38.p7 | 17:60218550 | ATTTAAATTATAATA[A/C]CATGCTGGTATTGTT | 84669 |
rs577225404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60225239 | CAGAGGACTGCTTGA[A/G]CCTGGGAGTTTGAGA | 84669 |
rs577252400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60183084 | CCCAACCAACCTGAT[G/T]TTCCAGAACAGAAGA | 84669 |
rs577286727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60242667 | CCACCTCTGCCTCCT[A/G]AAGTGCTGGGATTAC | 84669 |
rs577287356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60224187 | ATTTCAACTCTCAAC[C/T]ACATGCTAATCTTTG | 84669 |
rs577304863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60397673 | ACTACCTATTAGTAC[A/G]GTGCTTCCATTCTGT | 84669 |
rs577312895 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60246571 | CCCAGCAGTGGGATC[A/G]CTGGATAATATGGTG | 84669 |
rs577313170 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60182490 | GTTTTGGGCAAGGCA[C/T]AGTGGCTCACACCTG | 84669 |
rs577325136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60190255 | AAGCCAGGACCATGT[C/T]CTTGAACTTCCCAGG | 84669 |
rs577327655 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60324302 | TATATATATATATAT[-/AT]TTTAATTAAAAACTA | 84669 |
rs577328347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60344328 | AGAAATGGTGTTTTA[C/T]CATGTTGGCCAGGCT | 84669 |
rs577338198 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60279083 | TTTAATTACATAGAA[C/T]GTTTATGCTCCCTAT | 84669 |
rs577344007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60396783 | GGAGGTTCTCTTTTT[A/G]TTTTACTACAATCTA | 84669 |
rs577378627 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60243660 | GCCACTTAAAACGGT[A/G]AAAACATTTTTAGCT | 84669 |
rs577388297 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60297919 | GCTTTGACTGGACAA[C/G]AGAGCTATTTCAGTA | 84669 |
rs577396589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60241697 | TCTATTCAACTCTTT[C/T]ACACATTTTAAATTA | 84669 |
rs577405947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60357105 | AAAAACAAAACAATT[A/G]CAAAATTTGAAGACA | 84669 |
rs577430690 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60322190 | CTTTTTTTTAAGGTT[A/T]TTTTAAGATGAGTTC | 84669 |
rs577444556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60356202 | AACAATCAGTGGCAA[C/T]TATATAACTTCACAG | 84669 |
rs577460773 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60289734 | GGGAGAAGCAATTCA[C/T]AAGGAAATACAATGA | 84669 |
rs577465598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60343528 | AACTACATGGAAATT[C/G]AACAACCTGCTCCTG | 84669 |
rs577493750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404508 | TACAAGAAGACAATC[A/T]CGTTTCCTAAAAGAA | 84669 |
rs577501122 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60238580 | GACCGAGGCAGGCAG[A/G]TAACCTGAGGTCAGG | 84669 |
rs577533648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60387005 | TTAAAAGGCTTAACC[A/G]AAACCAACAATTCCA | 84669 |
rs577595264 | snp | A/G | 0 | 0 | intron-variant | USP32 | GRCh38.p7 | 17:60310322 | CCATTCATAATAGTC[A/G]AAGTTTGGAATTAAC | 84669 |
rs577600565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60327896 | GACGTGCTAGCTGCC[C/T]GCCACCTCAGCCCGC | 84669 |
rs577605170 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP32 | GRCh38.p7 | 17:60249995 | AGAGGCAAAATAAAA[A/T]AAAACTGAAAATGAA | 84669 |
rs577612110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60201137 | TGCTGAGATTACAGG[C/T]GTGAGCCACCGTGCC | 84669 |
rs577632424 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232429 | CTGCCTGCCTCAGCC[A/T]CCCAAAGAGCTGGGA | 84669 |
rs577657268 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60396950 | AGGAGAAGGGTCTTA[C/T]GGATAGTACCACCAG | 84669 |
rs577658277 | in-del | -/TTTTTTC | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60366148 | ACGCCGGGCTAAGTT[-/TTTTTTC]TTTTTTCTTTTTTCT | 84669 |
rs577669705 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60317534 | AAAAAAAAAAAAAAG[G/T]TAAAATGGTTAATTT | 84669 |
rs577693042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60185999 | TAGAGGTTGCAGTGA[A/G]CTGTGATTACACCAC | 84669 |
rs577712012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60187244 | AAACTAGCAAGGCTG[G/T]ATTTGATCGTGCAAT | 84669 |
rs577727931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60186382 | AGGAGAAATAACATG[A/C]AACACAGAAACCAGA | 84669 |
rs577744959 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP32 | GRCh38.p7 | 17:60239362 | TGAGCTTTTTGAACG[C/T]GTAGGTTCACGTCTT | 84669 |
rs577746094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231864 | TTGACACATTAAAGC[A/G]GGGAAAGACTGGTAA | 84669 |
rs577787793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60294091 | CCCACCCTCTGGTAG[A/G]GTCGGGGTCTTGCTA | 84669 |
rs577810146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60238540 | GGGCGCAGTGCCTCA[C/T]GCCTATAATCCCAGC | 84669 |
rs577813864 | in-del | -/ACACA | 0.103794 | 0.20279 | intron-variant | USP32 | GRCh38.p7 | 17:60388317 | CACACACACACACAC[-/ACACA]ACACACATCGCCTTA | 84669 |
rs577815326 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60367313 | CAGGAGTTCAAGACA[A/G]CTTAGGCAATATAAT | 84669 |
rs577859572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60277805 | AAATGCCAAAAACTT[C/T]CTTTATTTATTGGAA | 84669 |
rs577859686 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP32 | GRCh38.p7 | 17:60286940 | ATCACTTGAGGTCAG[C/G]AGTTTGAAACCAGCC | 84669 |
rs577881147 | in-del | -/AAAA | 0.370365 | 0.219117 | intron-variant | USP32 | GRCh38.p7 | 17:60386365 | TTTAGTTCATAAATT[-/AAAA]AAAAAAAAAAAAAAA | 84669 |
rs577888276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60401607 | TGGGGGCTGGGTGCA[A/G]TGGCTCACACCTGTA | 84669 |
rs577895423 | in-del | -/ATAAAA | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60319624 | CTCTACCAAAAAAAT[-/ATAAAA]ATTAGGCAGAAGTGG | 84669 |
rs577899665 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60288030 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGT | 84669 |
rs577911696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60302299 | TGGGATTACATGTGC[C/T]ACCATGCCAGGCTAA | 84669 |
rs577919278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60360033 | CCACCACACCTGGCT[A/C]ATTTTTTTGTATTTT | 84669 |
rs577929685 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60267077 | TACAGGCATGATGCA[C/T]GGTGCCAGGCCAGCA | 84669 |
rs577949980 | in-del | -/TAGAG | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418561 | AAAATAAATTATCAA[-/TAGAG]TAAACAGACAACCTA | 84669 |
rs577956218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60210323 | CTACTTTTTTTTTTT[A/C]TTTTTGGAGACAGAG | 84669 |
rs577961796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60400201 | AACTCCTGACCTCAG[G/T]TGATCCACCTGCCTC | 84669 |
rs577962102 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60284260 | GCCCTGTCGCCCAGG[C/T]TGGAGTGTAGTGGCA | 84669 |
rs577962479 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233018 | ACTATTAATCTCATT[G/T]TTCATATGTGAAAAC | 84669 |
rs577968099 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | USP32 | GRCh38.p7 | 17:60246412 | GTGTATATATATATA[A/T]ATTTTTTTTTTTTCT | 84669 |
rs577978058 | snp | C/G | 0.00161632 | 0.0283822 | intron-variant | USP32 | GRCh38.p7 | 17:60209320 | CTACATGTATTTGTG[C/G]CCAGAACATTTTGTC | 84669 |
rs577980575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414433 | TGTTTTATTGATTTA[G/T]TTGTTTATTTTTTGA | 84669 |
rs577985160 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60262278 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 84669 |
rs578013539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60254827 | TTATTTATTTTCTTT[A/T]AAAAAAATTCTCTTG | 84669 |
rs578024707 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60216810 | CAGTTTTTGAACACA[C/T]AGCAAGCAAATCTTT | 84669 |
rs578036272 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP32 | GRCh38.p7 | 17:60367842 | ATGCAGAAAAAATAA[C/T]GGATGGCTACCTCTG | 84669 |
rs578042646 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353838 | GAAAGGAAAATAAAA[G/T]TATGTAATTAACAAT | 84669 |
rs578048141 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60303390 | CCCCTAATATCCAGG[A/G]ACACAGCACCTGCCT | 84669 |
rs578091433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60267549 | TTTCTTTTTTTTGAG[A/G]TGGCGTCTCGCTCTG | 84669 |
rs578091813 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60368494 | TGCTTCAAACAAAAC[A/C]AGACTACTAGTTACA | 84669 |
rs578124234 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60392129 | CGCCTCCATGCCGGA[C/T]CACGTGACTCTTCCG | 84669 |
rs578134573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60325832 | TACTTGGGAGGCTGA[C/G]GCAGGAAGATTGCTT | 84669 |
rs578137128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60367024 | AGTAGAGACGGGGTT[C/T]CACCGTGTTAGCCAG | 84669 |
rs578137142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60376883 | ATCAGTTGGATAAAA[A/G]TTTTCTTCTATATAT | 84669 |
rs578145412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60334112 | GATGATTAGCACCTC[A/G]AATACTTACAGTACT | 84669 |
rs578166806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60333556 | AGTGAGCCAAGATTG[G/T]GCCACTGCACTCCAC | 84669 |
rs578201689 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60365727 | TAATTATTAAAAGAA[C/T]GCATTAAGATAAACC | 84669 |
rs578205305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP32 | GRCh38.p7 | 17:60223157 | AAATTCATACATAGC[A/G]TATGTGAAACAACAT | 84669 |
rs578229071 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP32 | GRCh38.p7 | 17:60184829 | AAAAAAAAAAAAAAA[A/C]CATATAAATATCTGA | 84669 |
rs578234306 | snp | A/T | | | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231406 | ATAAAGTAATAAAAT[A/T]ATTGTCTGATACAGC | 84669 |
rs578241138 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP32 | GRCh38.p7 | 17:60342143 | TTCTGTTTGTTCATT[A/T]TCCTTCTAACACTCA | 84669 |
rs745333817 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378502 | TTGTACACCAATGTT[C/T]ACAACAACATTATTC | 84669 |
rs745338143 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232661 | GAGCTATTCTTGTGT[C/T]TCAGCCTCCTGAGTA | 84669 |
rs745374484 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60283535 | GAAAGAAAGATGCAA[A/G]AAATATGTCTGAGTT | 84669 |
rs745375442 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265212 | AGCTTATAATAAATG[C/T]TTTCACATACAGTTT | 84669 |
rs745380717 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60228784 | AGTTGAGATCATGCC[A/G]CTGCACTCCAGCCAG | 84669 |
rs745388929 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60395268 | CAGGCCTGGCATCCC[C/T]TAAGGTCATAAAAAT | 84669 |
rs745389056 | snp | A/C | | | intron-variant, stop-gained | USP32 | GRCh38.p7 | 17:60377106 | CACCTACTACTCTCT[A/C]TATATATATGCCCAT | 84669 |
rs745396945 | in-del | -/AAAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60399662 | AGCAAGACCCTGTCA[-/AAAT]AAATAAATAAATAAG | 84669 |
rs745399940 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60322304 | GAACATACCACTATG[C/T]CTGGCTCCCTAAATC | 84669 |
rs745403152 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408480 | CCTCCCGGGTTCAAT[C/T]GATTTTCCTGCCTCC | 84669 |
rs745411386 | in-del | -/TA/TAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60180897 | TATTATTATTATTAT[-/TA/TAT]TTTGAGACAGGGACT | 84669 |
rs745433016 | snp | A/T | 1.64735e-05 | 0.00286993 | missense | USP32 | GRCh38.p7 | 17:60183254 | GAACTCTGCGCATCC[A/T]CTTTCTTCACCTCCC | 84669 |
rs745443601 | snp | C/T | 3.29804e-05 | 0.00406068 | missense | USP32 | GRCh38.p7 | 17:60223530 | TGTTATTGTCAGAAG[C/T]GTTATGTTGTCGAGC | 84669 |
rs745447432 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60277849 | CAGAATAGATATATG[-/T]TTTCTTCCAAATATT | 84669 |
rs745457397 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60247603 | TTGTCCTTTCTCTAA[C/T]GTATGCTCTTGGCAT | 84669 |
rs745464622 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60289876 | AATTAGTTACCTAAA[A/G]GAAATATGGTAGAAA | 84669 |
rs745481350 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60251357 | CTACTACTTTAAATA[A/T]CTATATCTTAATTGG | 84669 |
rs745481892 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60195247 | TTCCCAGTCCTCTGT[A/G]GCATTTGAAACGACT | 84669 |
rs745483703 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360751 | TGAAAAAAATGTGGT[G/T]GTTGTGCTGGGATTA | 84669 |
rs745484896 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60276948 | AGATTACATATACAT[-/AT]ATATATATATATATA | 84669 |
rs745488228 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60357236 | TGGGAGGACAGCTTG[A/T]GACCAGGAGTTCAAG | 84669 |
rs745490714 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60395588 | AGGAATTCTATTAAT[C/T]GTTTAGTTTGTTCAA | 84669 |
rs745505607 | snp | A/G | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420661 | TAAGAGCAAAACTCC[A/G]TCTCAAAAACAAACA | 84669 |
rs745530606 | in-del | -/TGAACCCAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60250044 | AACCCACAGATGAAA[-/TGAACCCAT]TTGGAACCAACAATT | 84669 |
rs745535363 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60303702 | TATATGAAGCACTTA[C/T]GTTTCAACCATAAAT | 84669 |
rs745544308 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60285029 | AATACCCTTAATTGC[-/A]AGTAGTCTTGAATAA | 84669 |
rs745568771 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60249498 | TTTATCCCCAAGCTG[G/T]TGATGTCAGTTTTCC | 84669 |
rs745568829 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60267064 | AAAGTGGTACGATTA[C/T]AGGCATGATGCACGG | 84669 |
rs745591299 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60318223 | TAATCTATTTAAACT[A/G]CAGTTTCCTTATAAA | 84669 |
rs745592664 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194103 | GCTGGAGTGCAGTGG[C/T]GCAATTATGGCTCAC | 84669 |
rs745603932 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60324931 | TGGCTTGAACCAAGG[A/C]GGCAGAATTTGCGGT | 84669 |
rs745604680 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360365 | AAAAAATTTTTGTAT[C/T]TGTATTTTGTATTAC | 84669 |
rs745625540 | snp | A/G | 6.59022e-05 | 0.00573993 | synonymous-codon | USP32 | GRCh38.p7 | 17:60180605 | TTTGGCATAAGTGAC[A/G]TAATGGCCCCCACCC | 84669 |
rs745634876 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60304119 | ACCAACTAGACAAAT[C/T]ACATTGAAACTTCTC | 84669 |
rs745639296 | snp | C/T | 5.07335e-05 | 0.00503629 | intron-variant | USP32 | GRCh38.p7 | 17:60219625 | GCTGCATTCTTAAGT[C/T]ACCTCTCGGTAAATG | 84669 |
rs745658170 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60290720 | ACAGCTGGGTGGGGG[G/T]CTGCTAGATAGCCTC | 84669 |
rs745679241 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60347353 | CCACACCTGGCTCAT[-/T]TTTTTTTTTTTTTTT | 84669 |
rs745679907 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60392200 | TCCTCTCTCTCCTCC[C/T]TCTCCTTCCCTCCTC | 84669 |
rs745699221 | in-del | -/ACAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60211567 | GTAATATGCCATGGC[-/ACAA]ACAGTTACTTATATT | 84669 |
rs745711350 | snp | A/C/G | 7.25168e-05 | 0.00602112 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231686 | TAGCTCTAAAGTTAC[A/C/G]TGATAACTAAATAGG | 84669 |
rs745712566 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60341927 | GTCAAGTGATTCTCC[A/G]TCCTGCTTTGTTCTG | 84669 |
rs745717932 | snp | A/C | 1.76197e-05 | 0.00296809 | intron-variant | USP32 | GRCh38.p7 | 17:60181287 | AAGTGAACAAAACAC[A/C]GACCACTCTCTGAAA | 84669 |
rs745724211 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60366746 | TCTCAAAAAAAAGTT[-/G]GTTTTTTTTTTTTCA | 84669 |
rs745750033 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60259487 | GTCTTGTCCAGGGTT[C/G]GTTCCTGTCTTGTAC | 84669 |
rs745759938 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60243583 | TTTATGTACACTGAA[A/C]TGTGAATTTTATATA | 84669 |
rs745761040 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60332853 | TCTGAGATTCATTCA[G/T]GTTGTTGCATATACC | 84669 |
rs745763779 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60390389 | GCCTAATTGAGGCCA[A/G]ACCTGTCAGGCTCAA | 84669 |
rs745781269 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60188518 | ACATATCATAAGCTT[C/G]TTCCCATAAATGTTA | 84669 |
rs745790033 | snp | A/T | 3.29843e-05 | 0.00406092 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271362 | TACCTTCACTTAGAG[A/T]TGGACGAATAGGTGG | 84669 |
rs745795346 | snp | A/C | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60421758 | CCCACCGCGTTTCCG[A/C]CCTCGGCCTCGGGTC | 84669 |
rs745804131 | in-del | -/CGCCGC | | | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60392104 | GCGGCTCCTCCCGGT[-/CGCCGC]CGCCGCCACCGCCTC | 84669 |
rs745832586 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60326475 | ACAACCATGCTCGGC[C/T]AATTTTTGTATTTTT | 84669 |
rs745834848 | snp | C/T | 1.69761e-05 | 0.00291337 | splice-acceptor-variant | USP32 | GRCh38.p7 | 17:60211516 | CTTTTCTGTGGGAAC[C/T]GGAACAAACAATATG | 84669 |
rs745842811 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60335968 | AGTTTCTCATAAAGA[C/T]TCACTTGGATAGGAT | 84669 |
rs745889742 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60399692 | TAAGTAAAAGTAAAA[C/T]ATAAAAATACAAATA | 84669 |
rs745895290 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60400776 | CTGTAATCCCAGCTA[C/T]TTGGGATGCTGAGTC | 84669 |
rs745898376 | snp | A/G | 6.65713e-05 | 0.00576899 | intron-variant | USP32 | GRCh38.p7 | 17:60214586 | AAACAAATACCAACA[A/G]TCAGACTCTCTATGA | 84669 |
rs745953202 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60399403 | CTCATACTTGTAATG[A/C]CAACACTTTGGGAGG | 84669 |
rs745976738 | snp | A/G | | | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402125 | TATTAGCTGCACCCA[A/G]TTTTGCATTGTACAA | 84669 |
rs746002121 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60356910 | AAAAAAAAACATGCC[C/T]AATGACTTCAAGTAT | 84669 |
rs746003083 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60300649 | AATAGACTACTATGT[C/T]TATGTCATCAGAATT | 84669 |
rs746025483 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60337293 | ACATGTTGATCACTA[C/T]GTCTAAAAACACTCC | 84669 |
rs746035512 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60273041 | TGGCGTGATCTCGGC[C/T]CACTGCAACCTCTGC | 84669 |
rs746043665 | snp | A/G | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424287 | CATGACGATGCTAGA[A/G]GCTAGGGATGCAAAG | 84669 |
rs746053861 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309308 | AAAAACAAAACAAAA[A/G]CAAACCCACAAAAAA | 84669 |
rs746065931 | in-del | -/GATT | | | intron-variant | USP32 | GRCh38.p7 | 17:60398754 | AGGCTGAGGCAAGAG[-/GATT]GATTGAGGTCAGGAG | 84669 |
rs746076148 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60385416 | GACAGTGTGGTGGCA[C/T]ACGCCTGTAGTCCCA | 84669 |
rs746105076 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60198036 | AGGTAAAAGATTAGA[A/G]AATGGAAGGATTATT | 84669 |
rs746121107 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60320965 | TGCTTTTTTTCCCCC[A/G]TCTCTGTCCTCTTAC | 84669 |
rs746121246 | in-del | -/CAGT | | | intron-variant | USP32 | GRCh38.p7 | 17:60311321 | GTAGCCATGACTATC[-/CAGT]CAAAGACTTAATACA | 84669 |
rs746154072 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60367970 | GAATTATAAGTAATC[C/T]AGAGATAACAGGAGG | 84669 |
rs746161253 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60348385 | GAAAGAAAATTGATA[C/T]GGAATAGTCAGGAGA | 84669 |
rs746174431 | snp | A/G | 1.70624e-05 | 0.00292077 | intron-variant | USP32 | GRCh38.p7 | 17:60252472 | GGTAAATCAAAGTTT[A/G]TTAACTGCATAATAT | 84669 |
rs746179325 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60300970 | TTGGGACTGACATCT[A/G]TCACTAAGCAAAATG | 84669 |
rs746213238 | snp | A/T | 3.51587e-05 | 0.00419262 | intron-variant | USP32 | GRCh38.p7 | 17:60209588 | ATTTCCTACCCATAA[A/T]ATTTGGAATGAACAT | 84669 |
rs746215934 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60293452 | AATCATAGCTCAGTT[C/T]GTCCTGAAGTAGTAA | 84669 |
rs746219878 | snp | A/G | 5.11104e-05 | 0.00505496 | intron-variant | USP32 | GRCh38.p7 | 17:60198220 | GATTATTTTTCTAGA[A/G]TTTGGAAACCACAGG | 84669 |
rs746230018 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256490 | AATGTTTCATTCAAT[A/T]TCATTTTATTATAAT | 84669 |
rs746236077 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60383549 | CTGTACACAAACTGT[C/T]CAGAATATTGCACAA | 84669 |
rs746265318 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60183968 | TTTTAATTGTATGCT[A/C]ATTATACCTCAATTT | 84669 |
rs746274947 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407053 | ACTGACGTCATTGAG[A/G]TAAAGAAAACAAATG | 84669 |
rs746276519 | snp | A/T | 1.6612e-05 | 0.00288196 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294775 | TAACATAGTTCCCAG[A/T]TTCACTTGAAAAAAG | 84669 |
rs746287376 | snp | C/T | 0.000142024 | 0.00842566 | intron-variant | USP32 | GRCh38.p7 | 17:60252358 | GTGAAATTTCAACTA[C/T]ATAATTGAAACTACA | 84669 |
rs746300702 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60282269 | GCTAACCAAAAGTTT[C/T]AGAAGGAAGACCTTA | 84669 |
rs746303914 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366043 | AGTGCAATGGCGCGA[A/T]CTCGGCTCACCGCAA | 84669 |
rs746307880 | snp | C/G | 1.65384e-05 | 0.00287557 | missense | USP32 | GRCh38.p7 | 17:60181594 | TTTGCTGGCATCCAA[C/G]TTCTCTTTACTACTT | 84669 |
rs746312766 | in-del | -/AT | 1.78979e-05 | 0.00299143 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231518 | CCCACTCAACTACAC[-/AT]GTCTGAGGCAGGAAA | 84669 |
rs746331736 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242561 | GACTACAGTCGTGTG[C/T]CACCATGCCTGGCTA | 84669 |
rs746331847 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60226559 | CTTCCTTATTTCCCA[C/T]AGTACATGAATGTAT | 84669 |
rs746333942 | in-del | -/TTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60343721 | CTAAAATCAACACTC[-/TTT]TAACATCACAATTAA | 84669 |
rs746366443 | snp | G/T | 3.33689e-05 | 0.00408453 | intron-variant | USP32 | GRCh38.p7 | 17:60294659 | GTCAATGAAAAGGGA[G/T]AAAATGTAAATCTTT | 84669 |
rs746374916 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60394030 | GGCAAACCAGATCAG[C/T]AGCGTGGCATTAGTC | 84669 |
rs746378362 | snp | C/T | 1.73972e-05 | 0.00294929 | missense | USP32 | GRCh38.p7 | 17:60181703 | GGGCTGCTGTTTTTG[C/T]TGGAGGGACAGCTGG | 84669 |
rs746394372 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60350338 | CTGTAGCCCAGGCTG[A/G]AGTGCAGTGGCATGA | 84669 |
rs746399035 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258044 | GGAAGAAGAAAAAAG[A/G]GAGCAAGCAGATAAG | 84669 |
rs746401689 | snp | C/T | 1.6686e-05 | 0.00288838 | missense | USP32 | GRCh38.p7 | 17:60214684 | CTTTGAGATAGATAT[C/T]CGTGAATTTCCTTGA | 84669 |
rs746411227 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60249606 | TCATGAATCAGACTG[A/G]CAGCCCATGCAGACT | 84669 |
rs746412958 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408364 | CTGAACTTGTAACCA[C/T]ATCGTATCAATCTGG | 84669 |
rs746434100 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60379731 | ATGAGCCACATGTTA[C/G]TTAACGTTCAGAAGA | 84669 |
rs746457499 | snp | G/T | 5.01534e-05 | 0.00500741 | intron-variant | USP32 | GRCh38.p7 | 17:60271517 | GATTATAAAACCTCA[G/T]AATTCTCTTCTCAGG | 84669 |
rs746506319 | in-del | -/TGTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60364389 | TTTTGAGGGGTTGTC[-/TGTT]TGTTTCAGACAGAAG | 84669 |
rs746506578 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60251743 | TTATCCTAAAGTAAA[A/T]CCTTAAGCCAAGACA | 84669 |
rs746518389 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305822 | ATGACTTTCAGTTTT[C/G]CAAGTACTTGTAAAA | 84669 |
rs746546282 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195434 | CTTCCACCTACAGGG[C/T]TGAAGCAATTCTCAG | 84669 |
rs746566118 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60316827 | GCCTGGGCAAAAGAG[C/G]GAGACTTTGACTCAT | 84669 |
rs746573411 | snp | A/G | 3.2969e-05 | 0.00405998 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271376 | GATGGACGAATAGGT[A/G]GTGAAACCAATGGGC | 84669 |
rs746574910 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360881 | CACCTATAATCCCAG[C/T]ACTTTGGGAGGCCAA | 84669 |
rs746583046 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60291977 | GAGTACATTTCATCT[A/G]GTATCCTACACCAGC | 84669 |
rs746584316 | snp | A/G | 1.82098e-05 | 0.00301738 | intron-variant | USP32 | GRCh38.p7 | 17:60183496 | GCATTAAAGGGTTCT[A/G]AAGATACAAAATTTA | 84669 |
rs746589138 | in-del | -/C | 1.64838e-05 | 0.00287083 | intron-variant | USP32 | GRCh38.p7 | 17:60198454 | CCTCATCTGTATGTA[-/C]AAACAAGAGAATAGA | 84669 |
rs746597842 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60276484 | CACTAGCTTTTTCAA[A/G]TTCTAAACTCTTCCA | 84669 |
rs746641889 | snp | A/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405348 | GCTGGGATTACAGGC[A/T]CACACCTCCAAGCCA | 84669 |
rs746654013 | snp | A/G | 0.000464684 | 0.0152357 | synonymous-codon, intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422625 | GCAAGGGGGTGAAGG[A/G]GACAAGCCACTAGAG | 84669 |
rs746664184 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388599 | CCAGTATCCATGAAG[C/T]ACAAGTGTACTTCCT | 84669 |
rs746681928 | snp | G/T | 1.64765e-05 | 0.00287019 | missense, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179311 | CTTCATCCATACTGC[G/T]TGTGTCTGCCATCTT | 84669 |
rs746687938 | snp | A/G | 1.65976e-05 | 0.00288072 | intron-variant | USP32 | GRCh38.p7 | 17:60225990 | AGAAAAGAAAGACCT[A/G]TCCAGGGGGAATAAA | 84669 |
rs746689628 | snp | C/T | 5.94513e-05 | 0.0054518 | intron-variant | USP32 | GRCh38.p7 | 17:60209362 | TTAGAAACTCAAAAC[C/T]GACAAACCTCTGCAG | 84669 |
rs746692959 | snp | A/G | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422665 | TGGGGTGTGAGGGAG[A/G]GAGGGAAGGAGGGTC | 84669 |
rs746700846 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60253362 | CTGTTCATACAAAAA[C/G]TTCGTACACTCAACA | 84669 |
rs746702610 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290794 | ATGATTAACCTCTAG[A/G]GAGGGAGGGGAGAGG | 84669 |
rs746709833 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60261751 | ATAAGAACCTTTTAT[A/G]TCTAACAGAACAAAA | 84669 |
rs746724929 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403857 | CCAGTCTGGGTAACA[C/T]AGTGAGACTCTATGT | 84669 |
rs746725190 | in-del | -/AAAAAAAAAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60372848 | GTGAGACCCTGTCTA[-/AAAAAAAAAA]AAAAAAAAAGACAAA | 84669 |
rs746732937 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60391620 | CATCCAGGATCACAA[A/C]GCCACCAGCGAGCAC | 84669 |
rs746762901 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60311910 | AACTGCTGCTTTCTG[A/G]TCCTGGTCATTCCAC | 84669 |
rs746766953 | snp | A/G | 3.55398e-05 | 0.00421528 | intron-variant | USP32 | GRCh38.p7 | 17:60211551 | CCAAAGCTTAGCTGT[A/G]GTAATATGCCATGGC | 84669 |
rs746795825 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60278514 | ATTATAAGCAGAGGT[A/G]AAACAGGATGTGTAA | 84669 |
rs746813664 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | USP32 | GRCh38.p7 | 17:60345525 | CAAGCACTTCCCGGA[C/T]GAAGCAGTGCTGGCC | 84669 |
rs746813689 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421116 | GGAACGTATGTAAAG[G/T]TTCCTTTCCCCTTGC | 84669 |
rs746817813 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60326604 | GTGCCCGGCCATGGT[C/T]TATTTTCTCATTCTA | 84669 |
rs746828961 | in-del | -/G | 0.00146988 | 0.0270699 | intron-variant | USP32 | GRCh38.p7 | 17:60222576 | TAGAATGACAATGTT[-/G]ACTTTCAATATTACA | 84669 |
rs746859349 | snp | A/G | 3.33089e-05 | 0.00408085 | missense | USP32 | GRCh38.p7 | 17:60219739 | GGAAGAGAAGATAGC[A/G]GGGAAATAATTCCAG | 84669 |
rs746869454 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60345327 | CTAAGAACACAGCCA[C/T]GTTGACATCTAAAAC | 84669 |
rs746882919 | snp | C/T | 1.65425e-05 | 0.00287593 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205501 | GCTGTCAGGAAGAGA[C/T]GGCATGTGACCATTA | 84669 |
rs746898615 | snp | C/T | 1.65252e-05 | 0.00287443 | missense | USP32 | GRCh38.p7 | 17:60212087 | CAGGCCAACTCATAT[C/T]TTTGTTGCGAACTGG | 84669 |
rs746900275 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60263132 | TTTTTTCTTTTTTTA[A/G]AGATAGAGTCTCGTT | 84669 |
rs746932622 | snp | A/G | | | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414037 | GTAGGATGTGGGTCC[A/G]GGTTTCTGAAAAACA | 84669 |
rs746933212 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60190877 | GTTTCAGGGAATCAT[C/G]CTTTTCATTTTTCAA | 84669 |
rs746941660 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60367816 | CTGTCTAAAACAAAA[C/T]AAAACCAAATATGCA | 84669 |
rs746949216 | snp | A/G | 1.6649e-05 | 0.00288518 | intron-variant, missense | USP32 | GRCh38.p7 | 17:60219633 | CTTAAGTTACCTCTC[A/G]GTAAATGCTGAGGAA | 84669 |
rs746989259 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417454 | CCAGCTGATTTTTAA[-/T]TTTTTTTTTTTTTTT | 84669 |
rs747003111 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60313020 | CTTTAGGAGGCTAAG[A/C]TGGGTGGATCACCTG | 84669 |
rs747004793 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60224614 | ACATGAGACCTCGTC[C/T]CTACAAAACAATTAA | 84669 |
rs747020387 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366402 | GACCTCGTGATCTAC[C/T]TGCCTCGGCCTCCCA | 84669 |
rs747035156 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60386816 | ATCTCCTCTTGTCAG[A/T]GACACACCAAACCTA | 84669 |
rs747036281 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60328173 | CTTTTCCAGGCACAG[A/C]AATCCATAGACCAAT | 84669 |
rs747054770 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60289512 | CCCAGAAGGCATCAC[C/T]GAAAACATGTATGTA | 84669 |
rs747059840 | snp | C/T | 4.96454e-05 | 0.00498199 | synonymous-codon | USP32 | GRCh38.p7 | 17:60214758 | CTTTAAAGGTGCATT[C/T]GGAGAAGGTACATTT | 84669 |
rs747075205 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308340 | GCTGCCCCTGGTGTC[A/G]GAGACCCATAACCTG | 84669 |
rs747093701 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60396505 | TAATCTGCAGTTAAA[G/T]AAATTTCTCCTCTCT | 84669 |
rs747126409 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60339293 | CATAAGTGCTAAAAG[A/G]TATAAATGGCCGAGC | 84669 |
rs747145160 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60397950 | TACCATGTGATTTAT[-/G]ATTCTAGGTTAAGAT | 84669 |
rs747149963 | snp | C/T | 3.55164e-05 | 0.0042139 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231562 | CACTCGTGGCAGTCC[C/T]GACGACGATCCTCGA | 84669 |
rs747157254 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309051 | AAAAAAACATTGGGG[A/G]AAATGCTCCAGGAGA | 84669 |
rs747180107 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60379050 | AACTATTTTGAAAGT[A/C]TTTTACAATAATCCT | 84669 |
rs747181082 | snp | C/T | 1.64825e-05 | 0.00287071 | synonymous-codon | USP32 | GRCh38.p7 | 17:60190578 | CCTTTCCTGGGATGT[C/T]TGATAGCGAAGGTGA | 84669 |
rs747191174 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60248958 | TTCTGAACCCCTGTG[G/T]GTTTTGTTTTGTTTT | 84669 |
rs747195166 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258274 | ACAATTTGGAAGCAC[A/G]GCAAAAAGAATTAAG | 84669 |
rs747218668 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264531 | AAAAAACAAACAGAC[-/A]AAAAAAAAAAACAAA | 84669 |
rs747219506 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408626 | CAAATGATCTGCCCA[C/T]CTCACCCTCCCAAAG | 84669 |
rs747234011 | snp | A/G | 3.47584e-05 | 0.00416869 | intron-variant | USP32 | GRCh38.p7 | 17:60226253 | TCAGGAAATCAGAGA[A/G]TAAGAAGCAAAGTTT | 84669 |
rs747234862 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60340414 | AAACCACGATTCTAC[-/A]AAAAAATACAAAAAT | 84669 |
rs747245527 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60204826 | CCCAGCCTGGAATGT[C/G]TGGGGCAAGCAAGCA | 84669 |
rs747251733 | snp | A/G | 1.74036e-05 | 0.00294983 | intron-variant | USP32 | GRCh38.p7 | 17:60181310 | CTCTGAAAACCATAT[A/G]ATAAACCACTTACCG | 84669 |
rs747262453 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60235987 | ACCATAGCAAGTATC[-/AT]ATAAACACTCATTTC | 84669 |
rs747268306 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309398 | TGAGCTCAGGAGTTC[A/G]AGACCAGCCTGGGCA | 84669 |
rs747282873 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60274617 | AACAGGGAAGAAGTA[C/G]TGAAAAAGAAAACAA | 84669 |
rs747288148 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60395607 | TAGTTTGTTCAATTT[C/T]ATTATAATTAACTTA | 84669 |
rs747309245 | snp | C/G | 0.000166237 | 0.00911542 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392592 | GACCGCAGAATCTTA[C/G]GGAATGGGGTTCTGA | 84669 |
rs747309438 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60331744 | GCAAAACAAAAAAAT[A/G]CAAGTTAGCCAGGCA | 84669 |
rs747314454 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60331575 | CATCTCAAAAAAAAA[-/T]AAAATAAACTTTAAT | 84669 |
rs747326572 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60244683 | GTCGCCCAGGCTGGA[G/T]AGCAGGCGTTCCATC | 84669 |
rs747339627 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60337055 | TGTTAGCCCTTAATG[C/T]TGGTAAGTCCAACAT | 84669 |
rs747340163 | in-del | -/T | 0.162553 | 0.234207 | intron-variant | USP32 | GRCh38.p7 | 17:60255299 | AACATCTTTTTTTTC[-/T]TTTTTTTTTTTTTTT | 84669 |
rs747345631 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60296905 | AAATCCTTAAAAACA[C/G]ATACTGGTCATGAGG | 84669 |
rs747350058 | snp | C/T | 1.64958e-05 | 0.00287187 | intron-variant | USP32 | GRCh38.p7 | 17:60198466 | GTACAAACAAGAGAA[C/T]AGAGAGTTCAGAAGA | 84669 |
rs747364925 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60282354 | CCCCTAAAAACATAG[C/T]ATACTCTTTTTTTTT | 84669 |
rs747374214 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60369751 | AGTTCTACACAATGA[-/T]TTTTTTTTTAAGAGA | 84669 |
rs747383001 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410300 | GACAGCTTTGACCCC[C/T]TATGATTTCATCCCT | 84669 |
rs747389781 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60285974 | AAGCCCCGTCTCTAA[C/T]AAAAATACAAAAATT | 84669 |
rs747408272 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60394232 | CAGCCTGCAGAGTGC[A/G]AGTTCCGAGTTAGAT | 84669 |
rs747409996 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242759 | ATCTCTATGATTCTC[C/T]TTATTCCAGTACTTG | 84669 |
rs747429429 | snp | A/G | 1.67002e-05 | 0.00288961 | intron-variant | USP32 | GRCh38.p7 | 17:60255282 | GAGACACTCATGTTA[A/G]GAACATCTTTTTTTT | 84669 |
rs747437357 | in-del | -/A | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415060 | TAGTCCTCTATAAAG[-/A]AAATAAATTTTTCGT | 84669 |
rs747437499 | snp | C/G | 1.74692e-05 | 0.00295539 | intron-variant | USP32 | GRCh38.p7 | 17:60183154 | ACCTGCATAAGGCCC[C/G]CAGGCCTCACCTTTC | 84669 |
rs747449360 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60229858 | TCGCTTTGTTGCCCA[A/G]GCTGGAGTGCAGTGG | 84669 |
rs747452085 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178467 | ACATTTCTGAGGATA[C/T]TTGAAGTATCCTAAA | 84669 |
rs747463249 | in-del | -/AGA | 1.65075e-05 | 0.00287289 | intron-variant | USP32 | GRCh38.p7 | 17:60345624 | CTGCAATTCAGAAAC[-/AGA]AGATGGGTAAGAAAT | 84669 |
rs747464928 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60350556 | GGCCTCCCAAATTGC[C/T]GGGATTACAAGCATG | 84669 |
rs747467477 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60318007 | AGAAAACAAACAAAC[-/A]AAAAAAAACAGCCAA | 84669 |
rs747488660 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404222 | GAGAGAGAGGTGGGG[G/T]AGAGGGAGAGAGAAT | 84669 |
rs747492436 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60283597 | AAGGAAAAGTCAAAG[C/G]TTAGTCAAGTTAGAC | 84669 |
rs747494849 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194190 | CTAGGATTACAGGCA[C/T]GCAACACCATACCTG | 84669 |
rs747515328 | snp | C/T | 1.66966e-05 | 0.00288929 | intron-variant | USP32 | GRCh38.p7 | 17:60255129 | GAAAAGATGTAGAAG[C/T]ACTGGTACTACTACC | 84669 |
rs747515702 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60321831 | ATGGTCAACTCTATT[-/A]ATCATTAACACCTCA | 84669 |
rs747517331 | snp | C/T | 1.6528e-05 | 0.00287467 | missense | USP32 | GRCh38.p7 | 17:60301650 | GGACAAGTCCAACTA[C/T]TAAATTATTGAAGTG | 84669 |
rs747521826 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60397228 | ATAATAACTTTGTCA[A/G]GTCACCTAAGTCCAG | 84669 |
rs747531811 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60269239 | ACTCCATTGTTAATA[-/G]GCAAATATCCCAAAC | 84669 |
rs747539117 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60316005 | TATCACAAGTCCACT[A/G]AACTTCTGATTCACA | 84669 |
rs747539467 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60243906 | TTTGTAACCTAAAAG[C/T]CATTTTCTTTTCTTA | 84669 |
rs747616627 | snp | C/T | 0.00197824 | 0.031388 | intron-variant | USP32 | GRCh38.p7 | 17:60249799 | TTTTTTAAGTGCTTT[C/T]GGGGAAAGGGTTGGC | 84669 |
rs747624839 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60292050 | AGATCACCAAATTTA[A/G]TGATCACTTCTCAGT | 84669 |
rs747629886 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60347107 | GCTACTACAAGAAAA[-/G]GGAGCTAAATTTGGG | 84669 |
rs747652756 | snp | C/T | 1.67604e-05 | 0.00289481 | synonymous-codon | USP32 | GRCh38.p7 | 17:60219755 | GGGAAATAATTCCAG[C/T]TCTGGGATGTCTGTC | 84669 |
rs747653141 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60308089 | CTCACCGTCCAGCTG[A/C]TGAGAGCTACTTCTA | 84669 |
rs747658578 | in-del | -/AA | 4.3917e-05 | 0.00468578 | intron-variant | USP32 | GRCh38.p7 | 17:60223591 | ATACAGAAAGCCTAT[-/AA]AAAAAAAAGAGGATA | 84669 |
rs747678179 | in-del | -/G | 0.000127915 | 0.00799632 | intron-variant | USP32 | GRCh38.p7 | 17:60208619 | TAAAGTAAATTTAAT[-/G]GAGTCAAGTAATTTT | 84669 |
rs747680390 | snp | C/T | 6.59022e-05 | 0.00573993 | missense | USP32 | GRCh38.p7 | 17:60180604 | TTTTGGCATAAGTGA[C/T]GTAATGGCCCCCACC | 84669 |
rs747690279 | snp | C/G | 3.77337e-05 | 0.00434344 | intron-variant | USP32 | GRCh38.p7 | 17:60211005 | TTATATTATTTTAAC[C/G]TGCTTACCCGAAGCT | 84669 |
rs747701203 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405597 | CAAAACCCCATCGCT[A/G]CAAAAATACAAAAAT | 84669 |
rs747701977 | snp | G/T | 2.19537e-05 | 0.00331306 | intron-variant | USP32 | GRCh38.p7 | 17:60288726 | TAGTCAAATTTTAAG[G/T]TATCTTACTTGGAAC | 84669 |
rs747704264 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191733 | CTAGGATGGTCTCAA[C/T]CTCCTGACCTCTTGA | 84669 |
rs747705982 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306632 | AACAGAGCAAGACTC[C/T]GTCTCGAAAGAAAAA | 84669 |
rs747709282 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182716 | TGCAGTGAGCTGTGA[G/T]CTGTGTTGCACCACT | 84669 |
rs747709348 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60254927 | TTGCAACTTATTCTC[C/T]ATATGTCTATGTACT | 84669 |
rs747712425 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60291284 | AAATCTGATTTTTTA[C/T]GTTTCTGAGTCATGG | 84669 |
rs747713946 | snp | C/T | 0.000198482 | 0.00995999 | intron-variant | USP32 | GRCh38.p7 | 17:60180506 | CAGTTCTGTTGATAT[C/T]CTGTTTCTAACTTTC | 84669 |
rs747742039 | snp | A/C | 1.64735e-05 | 0.00286993 | missense | USP32 | GRCh38.p7 | 17:60236216 | TGCTTGCAGACCATA[A/C]CTGCTCTCTCGTTCT | 84669 |
rs747749420 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392839 | CCCACCTTCTCCTCC[C/T]GACCATGCCTCTTGT | 84669 |
rs747762002 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328013 | AGGAGCAGCCTGGGA[A/G]CCATGGATGGCGGCA | 84669 |
rs747766743 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60262152 | TCTAAAGCAAATTCA[C/G]TGACTATATGGCTTA | 84669 |
rs747775681 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60224748 | TGATCATGCCATTGC[A/T]CTACAGCCTGGGCAA | 84669 |
rs747791843 | snp | C/T | 0.000609158 | 0.0174416 | intron-variant | USP32 | GRCh38.p7 | 17:60288479 | CCAGCCAATTATATA[C/T]ATAAAAAAAGGCAAA | 84669 |
rs747800694 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406728 | ACCATGTTGATCAAG[C/T]TGGTCTTAAACTCCT | 84669 |
rs747821511 | snp | A/T | 3.36355e-05 | 0.00410081 | intron-variant | USP32 | GRCh38.p7 | 17:60213700 | TTTTGTTATTTGGTT[A/T]GTAAACTTGAAACAA | 84669 |
rs747825492 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328139 | TAGTCCTGTGGACTG[A/G]AGTGGGAACTTGTGG | 84669 |
rs747849955 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295296 | TAAAATGAGATACAC[A/T]CAATGAAATACTACA | 84669 |
rs747859450 | snp | G/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419594 | AAAAATTAGCCGGGC[G/T]TGGTGGCAGGGGCCT | 84669 |
rs747861682 | snp | A/C | 5.06282e-05 | 0.00503106 | intron-variant | USP32 | GRCh38.p7 | 17:60211334 | ATATTGGGTTTATAT[A/C]AAAGTCACAGGTTAA | 84669 |
rs747871997 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60300834 | CCTGTACCCATTAGC[A/G]GTTGTTCTCCATTTC | 84669 |
rs747878007 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | USP32 | GRCh38.p7 | 17:60205607 | GGTCGGGGTAGGTCC[C/T]CATTGGTAGTTAGGG | 84669 |
rs747884393 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60263217 | CCTTCCAAAGTGCTG[G/T]GATTATAGATGAGAA | 84669 |
rs747896032 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60375200 | CTCTGTGGATACCAC[A/G]CTTCTTCTTACCCTA | 84669 |
rs747899691 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60239987 | AATTATCTGCGCCTT[A/G]GCCTCCCAAAGTGCT | 84669 |
rs747926052 | snp | C/T | 4.99147e-05 | 0.00499549 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266112 | GAAAAGAAACTCTTA[C/T]GGAGGAAAATCATTT | 84669 |
rs747935735 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60313266 | AAAAAATAAAATAAA[C/G]TAAGATTAAAAAAAT | 84669 |
rs747936012 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265993 | GAATATCATCAGTGC[A/G]GTTGTCCTTCCAGAC | 84669 |
rs747949725 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373729 | GTGTTGGGTTACAAG[C/T]GTGAGCCACCATGCC | 84669 |
rs747960590 | snp | C/G | 1.64795e-05 | 0.00287045 | missense | USP32 | GRCh38.p7 | 17:60183366 | CCAAAAAAGCACTTG[C/G]ATCAAAACTTTCCCG | 84669 |
rs747964018 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191061 | ATTTATCTGGTGTAA[C/T]ACCTAGCTCCTTGTC | 84669 |
rs747968135 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60226308 | CAGAAACAAATCTCA[C/T]AATTATCTATTTTTT | 84669 |
rs748012381 | snp | A/C | 0.000150259 | 0.00866643 | missense, intron-variant | USP32 | GRCh38.p7 | 17:60391894 | CACCTCTCCTCAGCG[A/C]CTCCTCGTAGCTGAG | 84669 |
rs748025912 | snp | C/T | 3.43424e-05 | 0.00414367 | intron-variant | USP32 | GRCh38.p7 | 17:60391835 | CACCCTCCAGGCTGC[C/T]CGTCGCGGGCCTCCC | 84669 |
rs748041533 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60270195 | ACAATTTTGTTTTCA[A/T]ATGAAATGATACATC | 84669 |
rs748047163 | snp | C/T | 1.73225e-05 | 0.00294295 | intron-variant | USP32 | GRCh38.p7 | 17:60205708 | TTGTGGTATTTTCAT[C/T]TTTGCTCTTTTCTCA | 84669 |
rs748052764 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60249060 | TCTTCGTGTTTTCTT[C/T]TTTATTATCTGTTTT | 84669 |
rs748058004 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60358411 | AAAACCCCATCTCTA[C/T]CAAAAATACAAAAAT | 84669 |
rs748096706 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60400815 | CACTTGTGGCCAGGG[A/G]TTTGAGACCAGCCTA | 84669 |
rs748097317 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60338183 | ACAAAAAATTAGCTG[A/G]GCATGGTGGTACATG | 84669 |
rs748127837 | snp | A/C | 1.69723e-05 | 0.00291305 | intron-variant | USP32 | GRCh38.p7 | 17:60255285 | ACACTCATGTTAGGA[A/C]CATCTTTTTTTTCTT | 84669 |
rs748141290 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60204466 | TGGCTTAGGAGATAC[-/T]TTTTTTTTTTTTTTT | 84669 |
rs748147491 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60301880 | CCTTATTATTGCACT[C/T]AGCCTAGAATAGACT | 84669 |
rs748161759 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264813 | GGCAGTGAGCTGAGA[G/T]CCTGTCAGTGCACTC | 84669 |
rs748162808 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60310559 | CAAAAATTAGCTGGG[C/T]GTGGTGGCACGCGCC | 84669 |
rs748166995 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60276081 | GGAATGGGATCTAAT[G/T]TTTAAAATATATAAC | 84669 |
rs748187150 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388166 | ACACACTATAGTTCA[C/T]CACTCAGCTACTAAG | 84669 |
rs748198875 | snp | G/T | 1.66225e-05 | 0.00288287 | intron-variant | USP32 | GRCh38.p7 | 17:60192824 | TTCTACTAAAGTAAT[G/T]CTTTTGCAGGTCACT | 84669 |
rs748200075 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60350914 | TTTTTTTTAACTCAC[A/G]AAGACAAAAATAGGA | 84669 |
rs748204158 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60247886 | AGACGGGGTTTCACC[A/G]CGTTAGCCAGTATGG | 84669 |
rs748215660 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258505 | CAATCTGCATCAGCC[A/G]TTATGATGGATTTAA | 84669 |
rs748237830 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60336896 | GTTGTTCTGTCAGCT[A/G]TGATGTCAAGATCAA | 84669 |
rs748266342 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60324701 | TTTGTCTCAGAAAAT[C/T]ATACTAAAAAACTGT | 84669 |
rs748291005 | snp | C/G | 1.69117e-05 | 0.00290785 | intron-variant | USP32 | GRCh38.p7 | 17:60192970 | GTGTAAGAAGCATTT[C/G]TGGTTCGAGGTCCAA | 84669 |
rs748319238 | snp | A/C | 1.64732e-05 | 0.0028699 | missense | USP32 | GRCh38.p7 | 17:60181447 | GCCACATGCTTCATG[A/C]TCATAAAGGAATCCA | 84669 |
rs748321912 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60244570 | TATTTTGGGGGATCA[C/T]TTTCTTAGAGATTGT | 84669 |
rs748324663 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283892 | TGATGAAGCAAAGAA[C/T]GTACATCATCCGAGA | 84669 |
rs748328428 | snp | C/T | 1.79693e-05 | 0.00299739 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231664 | AAAGGTGATTTAAAG[C/T]ATCTTCTAGCTCTAA | 84669 |
rs748350652 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60297175 | TGCCAAGACGAGAGA[A/G]TCATTTGAGGCCAGG | 84669 |
rs748354476 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60395896 | AGAGAGGGAGGTCAA[C/T]ACAATAGAAGTGGAA | 84669 |
rs748374205 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60189389 | GTTACCGTTACTAAC[G/T]TATCCAAAGGGAATG | 84669 |
rs748393495 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60266320 | TTATTCAGATATAAG[-/A]CCCTACCCTTCAGCC | 84669 |
rs748400291 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60243693 | CAGATTGTACAGAAT[C/T]AGGCAGTGGGACAAA | 84669 |
rs748406892 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60311794 | TGCACCATTGCACTC[C/T]AGCCTGGGCAACAAG | 84669 |
rs748414839 | snp | C/T | 1.65616e-05 | 0.00287759 | intron-variant | USP32 | GRCh38.p7 | 17:60212118 | AAGGACAGATAGGAA[C/T]GTGTTAATTTCTTAT | 84669 |
rs748432076 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60333168 | AATCTGAGTATAACT[G/T]TGGACTCCAGAAAAG | 84669 |
rs748482647 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60285808 | TTTAACACGTAGAAG[-/A]AAAAGAGAAGGCATT | 84669 |
rs748492212 | snp | C/T | 6.58968e-05 | 0.00573969 | missense | USP32 | GRCh38.p7 | 17:60183245 | TCCCCAGCCGAACTC[C/T]GCGCATCCACTTTCT | 84669 |
rs748503707 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178540 | CCAGGATGCTGTTTC[C/T]TTCTACTGGGTCTCC | 84669 |
rs748515925 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60397382 | TTGTTGTTGTTTAAG[A/G]CACAGCGTCTCTCTC | 84669 |
rs748517862 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245885 | AAAGCTTTAAAAATA[G/T]TTCTATTAAAAAATT | 84669 |
rs748529981 | in-del | -/C | 3.63875e-05 | 0.00426526 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391988 | CTGATCTCGCCCCCA[-/C]CCCCCTCCCGCCTTC | 84669 |
rs748531546 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60317927 | GAGGCAGAGATTGCA[A/G]TAAGCTGAGATGGTG | 84669 |
rs748548257 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230039 | GGCTGGTCTTGAACC[C/T]CTGACCTCAGGTGAT | 84669 |
rs748565641 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60253507 | TTGGTGGCTCATATC[C/T]ATAATCCTAGCACTT | 84669 |
rs748572931 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60321654 | AATGAATGGAAACAC[-/A]ACAGTTTAAACATAG | 84669 |
rs748580586 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404087 | AGAAAAAGAAATATG[C/T]GCACACACACATATT | 84669 |
rs748591655 | snp | A/G | 1.74586e-05 | 0.00295448 | synonymous-codon | USP32 | GRCh38.p7 | 17:60208188 | TCCATACCGTACAGG[A/G]GTAGTACCATCTAAC | 84669 |
rs748609853 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60221153 | AATACCAGCACTTTG[C/G]GAGGCCAAGGCAGAA | 84669 |
rs748610927 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60248887 | TATTCCATGTCTCAT[-/A]ATTTTTTCTTGTTGA | 84669 |
rs748631178 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178843 | GGTAGCATATCATGT[C/T]GTCCCTAGACAACAT | 84669 |
rs748655778 | snp | C/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422845 | TGATGGGGAAGAGGT[C/T]GCCTCTCATTGTTGG | 84669 |
rs748661391 | snp | C/T | | | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231209 | TCACCTTTTTCTCTA[C/T]TGATGATACTACTAC | 84669 |
rs748668187 | snp | C/T | 1.65089e-05 | 0.00287301 | synonymous-codon | USP32 | GRCh38.p7 | 17:60223561 | AAAGCAAACATCTGC[C/T]CCTGGTGTGGCAGAA | 84669 |
rs748685782 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306076 | TAAGTACCCTTTTTT[A/C]ACTCAAAAAGAAAAA | 84669 |
rs748702503 | snp | C/T | 1.65638e-05 | 0.00287778 | intron-variant | USP32 | GRCh38.p7 | 17:60180689 | TAACTGTACTATGGC[C/T]AGGGTATAGCACTAG | 84669 |
rs748704018 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245229 | TATTGGTGCTCTTTA[-/T]TTTTTTTTTTGGCAG | 84669 |
rs748707266 | snp | A/G | | | upstream-variant-2KB, missense, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421444 | GCCCGGGCCGACGGC[A/G]GTCCCACCGCACTGT | 84669 |
rs748729253 | snp | A/G | 1.68434e-05 | 0.00290197 | intron-variant | USP32 | GRCh38.p7 | 17:60211344 | TATATCAAAGTCACA[A/G]GTTAAGAGGCCAGTG | 84669 |
rs748734595 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411722 | TATTTTAGATATTTC[A/C]TATAAGTGGAATTAT | 84669 |
rs748746032 | snp | A/G | 1.66715e-05 | 0.00288712 | synonymous-codon, intron-variant | USP32 | GRCh38.p7 | 17:60391910 | CTCCTCGTAGCTGAG[A/G]AATCCGATCCGTGAC | 84669 |
rs748751451 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60224905 | TCTTCCTTGTAGGTG[A/T]GGAAACATGAAGTTT | 84669 |
rs748754291 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393780 | ACCTCTGCCTCTCTG[A/G]TTCAAGCGACTCTCC | 84669 |
rs748761018 | snp | C/T | 3.39432e-05 | 0.00411952 | intron-variant | USP32 | GRCh38.p7 | 17:60223383 | CTTGCAAGAGAATAA[C/T]TTTAAGTTTAGATGT | 84669 |
rs748772883 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60329317 | TCCTAAGAGTTCCAG[A/C]GGGGTCTTAGGATAG | 84669 |
rs748794134 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60294582 | AATGCCAAGAGTAAT[C/G]TGCACATAAACATCT | 84669 |
rs748811303 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407924 | CCAACATGGTGAAAC[C/T]TCGTCTCTACTAAAA | 84669 |
rs748817813 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290795 | TGATTAACCTCTAGG[A/G]AGGGAGGGGAGAGGG | 84669 |
rs748818751 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328363 | CTGAGAGCTGGACCG[A/G]GGATGGGATGACCAG | 84669 |
rs748819237 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60333142 | GGGCACAACTCCCCG[-/C]CAAGGTTGAAAATCT | 84669 |
rs748821396 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60241204 | GGGTTCCATCATGTT[A/G]GCCAGGCTGGTCTCG | 84669 |
rs748822775 | snp | C/G | 1.65004e-05 | 0.00287227 | intron-variant | USP32 | GRCh38.p7 | 17:60198470 | AAACAAGAGAATAGA[C/G]AGTTCAGAAGACAGG | 84669 |
rs748842597 | in-del | -/TTC | 0.000301453 | 0.0122734 | intron-variant | USP32 | GRCh38.p7 | 17:60255296 | AGGAACATCTTTTTT[-/TTC]TTTTTTTTTTTTTTT | 84669 |
rs748858005 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60375616 | GTTGTTTGTTTGTTT[C/G]TTTTTGTGATGGAGT | 84669 |
rs748858714 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60380573 | GTCATTCCAGATAAG[-/A]GAAATCACAGAAATA | 84669 |
rs748877739 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416221 | ATCACTGGTCAACCC[A/C]GAAAGAGAGATGGGC | 84669 |
rs748940986 | snp | C/T | 2.07136e-05 | 0.00321813 | intron-variant | USP32 | GRCh38.p7 | 17:60252349 | TTCAAGTATGTGAAA[C/T]TTCAACTATATAATT | 84669 |
rs748956245 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60186659 | TTTGGGGTCCTGTTA[A/G]TCAGCATGTTAGGCT | 84669 |
rs748987731 | snp | G/T | 1.66549e-05 | 0.00288568 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205477 | TGCAATGATGTAACC[G/T]GTAAAGGGGCTGTCA | 84669 |
rs749005912 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60325492 | GAATATTTACATAGT[C/T]ATAATATTGTAAATA | 84669 |
rs749018694 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60339457 | GCGTGGTGGTGGGCA[C/T]CTGCAATCCCAGCTA | 84669 |
rs749020060 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60263445 | TAGTCACCAGCGAAT[A/G]TGGTTAATAGGCTTG | 84669 |
rs749049002 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60360369 | AATTTTTGTATTTGT[A/C]TTTTGTATTACAGGC | 84669 |
rs749049496 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60279784 | GGAGGTTGCAATGAG[-/C]CTAGATAGGGCCACT | 84669 |
rs749066080 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60400971 | GAGACCAGCCTGGCC[A/G]ACATAGCAAAACCCC | 84669 |
rs749066699 | snp | C/T | 7.30007e-05 | 0.00604111 | missense | USP32 | GRCh38.p7 | 17:60207108 | TCACTGAGAGTCGTA[C/T]TTTTTGGTTGTCCTG | 84669 |
rs749072389 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60194083 | GGTATCACTCTGTTG[A/C]CCAGGCTGGAGTGCA | 84669 |
rs749074954 | in-del | -/AA/AAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60196270 | TTCTATCCCCACGCC[-/AA/AAA]AAAAAAAGAAAAAAA | 84669 |
rs749075669 | in-del | -/TG | | | intron-variant | USP32 | GRCh38.p7 | 17:60380887 | CCTTGCATATAAGGC[-/TG]TGTTTCATTTTTCCT | 84669 |
rs749081759 | snp | A/G | 1.83687e-05 | 0.00303051 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231473 | TCATTTGTAAATTCA[A/G]AGAAGAGAGGTGTTT | 84669 |
rs749096205 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60360987 | TACAAAAATTAGCCA[A/G]GTGTGGTGGCACATG | 84669 |
rs749102405 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60398455 | AGTCACTGGTGTTCT[G/T]GCCGGAGGGAAGCAA | 84669 |
rs749102974 | in-del | -/CA | | | intron-variant | USP32 | GRCh38.p7 | 17:60230521 | CAACTGCGGTTCTAC[-/CA]CATGCTTTTAACATG | 84669 |
rs749104149 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179367 | TGTGCATAGTCTATC[C/T]CCTGCTGCTCATAGA | 84669 |
rs749109778 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417302 | TTATGAAGTGTAGCA[C/T]ACATACCCTTTTATG | 84669 |
rs749128520 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60369610 | ATTGGCAGATCTGAC[-/AT]ATACAAAATTTTAAC | 84669 |
rs749138521 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60285104 | TAACACAACAAGGCA[-/T]TTAAGGAAAGCAGTC | 84669 |
rs749143412 | snp | C/T | 1.66178e-05 | 0.00288247 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269530 | TCTATGTGATTGTCA[C/T]GATTTTCATCAAAAG | 84669 |
rs749143576 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60315638 | GCCAATATTCACAGC[A/G]GCATTATTGACAATA | 84669 |
rs749169985 | snp | C/T | 1.65239e-05 | 0.00287431 | missense | USP32 | GRCh38.p7 | 17:60185612 | TGGGCTCGGCTTGCG[C/T]TCGCCGACTCTGCTC | 84669 |
rs749181957 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60213916 | GGGGAACAGGTGGTG[-/T]TTGGTTACATGAATA | 84669 |
rs749182481 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60274660 | CCAATTCTGTATCAC[A/G]TGAAAATATTCTTCA | 84669 |
rs749196529 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60204620 | GCTACAGGCGCATGC[C/T]ACCATGCCCAGCTAA | 84669 |
rs749214643 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60236582 | TTCAAAACAGCCTTA[C/T]TGAGGAATAATTTAC | 84669 |
rs749228877 | snp | C/T | 1.67826e-05 | 0.00289673 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266128 | GGAGGAAAATCATTT[C/T]TGTATTCTGAGGTAT | 84669 |
rs749230927 | snp | C/T | 1.72791e-05 | 0.00293926 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391984 | GAGCCTGATCTCGCC[C/T]CCACCCCCCTCCCGC | 84669 |
rs749246879 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60323213 | ACAGCAGCATTATTT[A/G]TAATAACAAAAAAGT | 84669 |
rs749248804 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60341826 | TTTCAAGGTTTTTTA[A/G]CTTCCTTGCGATGGG | 84669 |
rs749261759 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant | USP32 | GRCh38.p7 | 17:60180538 | TTCAAAGACTGAGAA[C/T]GTTTACCTTACAGCT | 84669 |
rs749282473 | snp | C/T | 0.0284313 | 0.11579 | missense | USP32 | GRCh38.p7 | 17:60211035 | TTTAATGGGGCAACA[C/T]TCTTCTGAGTTCCAC | 84669 |
rs749284778 | snp | A/G | 3.30923e-05 | 0.00406756 | intron-variant | USP32 | GRCh38.p7 | 17:60226020 | ACCAATAAACCTCAG[A/G]GGAATAGGTCATATT | 84669 |
rs749292711 | snp | C/T | | | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402452 | GACAGGGCTTCACCA[C/T]GTTGCCCAGACTGGT | 84669 |
rs749296534 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60266431 | TTTTAGGAAGTAATG[A/C]AAACCCCTAGGTTAA | 84669 |
rs749300132 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60395825 | TACTCACAGAGAAAT[G/T]ACATAAGAATAGGAC | 84669 |
rs749304491 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60235266 | ATGACTGATGCTGTA[C/T]CCCAATATTCTCATT | 84669 |
rs749310355 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60354047 | AAGAAATCACATGCA[C/T]GTGTGAAATGCATGA | 84669 |
rs749313392 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60261375 | ATGTAGGCCAGGCAC[A/G]GTGGCTCACACTTGT | 84669 |
rs749332349 | snp | A/G | 3.29843e-05 | 0.00406092 | missense | USP32 | GRCh38.p7 | 17:60181557 | CGTCAGCCAGCTCAC[A/G]TATCTGCCCAGCCCC | 84669 |
rs749370277 | snp | C/T | 1.6591e-05 | 0.00288015 | intron-variant | USP32 | GRCh38.p7 | 17:60212131 | AATGTGTTAATTTCT[C/T]ATCTATCTAATTTAT | 84669 |
rs749373523 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60244734 | CCTCCTGGGTTCAAG[C/T]GATTCTCCCACCTCA | 84669 |
rs749390138 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60372065 | CAGGGAGAGGGGAAG[A/G]GGAAGTGGCTAAGGT | 84669 |
rs749390724 | in-del | -/GTCT | | | intron-variant | USP32 | GRCh38.p7 | 17:60237123 | CTACTCTATCTATCT[-/GTCT]ATCTATCTATCTATC | 84669 |
rs749405806 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60279492 | CTCAAAAAAAAAAAG[-/A]AAAAAAAAACCTTAT | 84669 |
rs749415808 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60311851 | AAAAAAAACGGTAGA[C/T]ATGTGTAGGTCTCCA | 84669 |
rs749433707 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60352877 | AACTCAACTGAACAG[C/G]GTTCACTGAATAATT | 84669 |
rs749456034 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60270259 | ACTGTTGTTGAAGTA[C/G]GTAGAAACCCAGAGC | 84669 |
rs749462973 | snp | C/G | | | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231414 | ATAAAATAATTGTCT[C/G]ATACAGCTTTGGGCA | 84669 |
rs749463207 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60286340 | TAAGGATCTTGAGGT[A/T]AAATTATCCTGGATT | 84669 |
rs749512665 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60246142 | ATCCAACTGTATTTT[C/T]ACAGTCATTAACTAA | 84669 |
rs749529054 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403759 | CATACAGAAACATGG[G/T]CCGGGAGCAATGGCT | 84669 |
rs749532153 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60243229 | CCTGTCATGTTGCTG[-/A]ACTCATTTTATTAAT | 84669 |
rs749537765 | snp | A/G | 1.64838e-05 | 0.00287083 | missense | USP32 | GRCh38.p7 | 17:60219703 | TAGACTGCTGTGTCC[A/G]AGTGGCAGGCTGCTG | 84669 |
rs749538419 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60300323 | AGAAGACCTTATAAA[C/T]AATTAAATGAATGAA | 84669 |
rs749548188 | snp | A/T | 3.4782e-05 | 0.00417011 | intron-variant | USP32 | GRCh38.p7 | 17:60206986 | ACAAATATTTAAAGG[A/T]GCAATCATGAGAAGG | 84669 |
rs749564201 | snp | C/T | 5.02828e-05 | 0.00501387 | intron-variant | USP32 | GRCh38.p7 | 17:60294638 | ACAACTAAGAGTTAA[C/T]ACTTTGTCAATGAAA | 84669 |
rs749616217 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60365247 | GTACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAT | 84669 |
rs749641360 | snp | A/G/T | 5.00984e-05 | 0.00500471 | missense | USP32 | GRCh38.p7 | 17:60214664 | CTTCCTCTTTAATGC[A/G/T]CAGCCTTTGAGATAG | 84669 |
rs749650078 | snp | A/G | 2.13067e-05 | 0.00326388 | missense | USP32 | GRCh38.p7 | 17:60208735 | ATCGGACACTTATAT[A/G]CCCACATGTCTTGCA | 84669 |
rs749650949 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60220065 | AAAAAAAAAAACCCT[A/G]AGTATTATCTATAAT | 84669 |
rs749658871 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60196800 | ACTGCACTCCAGCCT[A/G]GGTGACAGAGCGAGA | 84669 |
rs749659045 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232888 | TAACTACTGCTACTA[C/T]TACCACCATTATTAC | 84669 |
rs749659291 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60271798 | CACTTTTACCTGTAC[C/T]GATTTTTTTTCTTCT | 84669 |
rs749672996 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60350441 | TTACAGGCACCTACC[A/G]TAACACCTGGGTAAG | 84669 |
rs749686302 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60311516 | TCTTGTCTAACAGTT[-/AA]GAGGTCAAAAAAGGG | 84669 |
rs749686663 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60294224 | AGATGACAATTTTTT[A/C]ACACAAATATTTCAC | 84669 |
rs749690478 | snp | C/T | 6.85158e-05 | 0.00585263 | intron-variant | USP32 | GRCh38.p7 | 17:60209332 | GTGGCCAGAACATTT[C/T]GTCTATTGCTTACAT | 84669 |
rs749701471 | snp | A/G | 1.66763e-05 | 0.00288753 | intron-variant | USP32 | GRCh38.p7 | 17:60288501 | AAAGGCAAACAGAAA[A/G]CAATGAAATGTCATT | 84669 |
rs749701629 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60319255 | AATATTATGTTTTAT[A/T]TATTTTGCCACAACA | 84669 |
rs749706406 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60338038 | GCTAAAATTGTTGGA[C/T]GCAGGCAAGGCGTGG | 84669 |
rs749709123 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60240387 | CATTTCACTTGTGTT[C/T]GAAGAGCTAGTATTT | 84669 |
rs749724604 | snp | C/T | 1.6504e-05 | 0.00287258 | missense | USP32 | GRCh38.p7 | 17:60192844 | TGCAGGTCACTTTAC[C/T]TATACCATGGGCACC | 84669 |
rs749731795 | in-del | -/ATAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60383673 | GACATGTAAAAATTC[-/ATAA]ATAGTCTTTCCAGGA | 84669 |
rs749740114 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60237002 | AACACCTAAAGAACA[-/T]TTGAAACTGGCAAGT | 84669 |
rs749772015 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60256414 | CTTACAGCAGAGGAA[A/G]TGCTGTGATAAGGTT | 84669 |
rs749797018 | snp | G/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424068 | CAAGAGAGAGAGGAG[G/T]GCGTGTCAGGCTCTT | 84669 |
rs749798676 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406890 | AGACTGACATGCTAA[C/T]CAAATTTCAGTGAAA | 84669 |
rs749809603 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | USP32 | GRCh38.p7 | 17:60226122 | TTCACGTAACTGAGG[C/T]TGCTTCCAATTCTAT | 84669 |
rs749830854 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60347894 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACGAGGT | 84669 |
rs749869681 | snp | A/T | 1.86932e-05 | 0.00305716 | intron-variant | USP32 | GRCh38.p7 | 17:60223618 | GGATAGAATCTCTTA[A/T]TTTTAGTTATTATAC | 84669 |
rs749877435 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353408 | CTGACTACTATCATT[A/T]CTATAGTACCAATGG | 84669 |
rs749894070 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60298003 | TTCTGGCTGGTTTAC[A/G]GAGGCTGCTCACTTG | 84669 |
rs749908641 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60260372 | CTAAAAATACAAAAA[A/C]ATTAGCTGGGTGTGG | 84669 |
rs749920052 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60333431 | TGGTGAAACCCCCAT[A/C]TCTACTACAAATACA | 84669 |
rs749953885 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60243713 | AGTGGGACAAAGTTG[A/G]TCAATATGCCATAGT | 84669 |
rs749961314 | snp | C/T | 1.65091e-05 | 0.00287303 | intron-variant | USP32 | GRCh38.p7 | 17:60255307 | TTTTTTCTTTTTTTT[C/T]TTTTTTTTGAGACGG | 84669 |
rs749970262 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60401338 | TCGCGCCACTGCACT[A/C]CAGCCTGGGCGACAG | 84669 |
rs749983705 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60189034 | ACACTGGATTTGTTA[A/G]AAAGGGGAAGAGATT | 84669 |
rs750000003 | snp | G/T | 1.64735e-05 | 0.00286993 | missense | USP32 | GRCh38.p7 | 17:60205584 | GCATTCCATTGGGGA[G/T]GAATATTGGTCGGGG | 84669 |
rs750014077 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60379460 | CTACCCTTTCAAAAG[-/T]TTAGCTTATCTCTGC | 84669 |
rs750034355 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60269301 | TTCCTTAGAGTGACC[G/T]CAGTAAAACCCTAAC | 84669 |
rs750066161 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230832 | TTTCCTTCTATAAGA[C/T]GAACAAACCAATCAC | 84669 |
rs750068767 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60398313 | AGGTGGGAGGATCAC[C/T]TGGGCCTGAAAAGTA | 84669 |
rs750088957 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60225490 | ATTTCCATATTGAGA[-/T]GATTTAATGAAGTAT | 84669 |
rs750095402 | snp | G/T | 0.000132701 | 0.00814449 | intron-variant | USP32 | GRCh38.p7 | 17:60255278 | AACAGAGACACTCAT[G/T]TTAGGAACATCTTTT | 84669 |
rs750107140 | snp | G/T | 1.70764e-05 | 0.00292197 | intron-variant | USP32 | GRCh38.p7 | 17:60301750 | AGGCATTTCAGTTGT[G/T]GAGGAATCTGAGGCA | 84669 |
rs750111932 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60268522 | AGGTTACAGTGAGCT[A/G]CGATCACACCACTGC | 84669 |
rs750116164 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60197581 | TGCACTCCAATCCGG[C/G]CAACAAGAGCAAAAC | 84669 |
rs750138751 | snp | G/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423340 | TGGGATTACAGGTAT[G/T]CATTACCACACCTGG | 84669 |
rs750149203 | snp | A/G | 1.6631e-05 | 0.00288362 | synonymous-codon, intron-variant | USP32 | GRCh38.p7 | 17:60288650 | GTTTAGAAAAAGCCA[A/G]TTTCTAAACTTTTCA | 84669 |
rs750162288 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60229838 | TCTTTTTTTGAGACA[A/G]AGTCTCGCTTTGTTG | 84669 |
rs750164726 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60179796 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 84669 |
rs750171827 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405144 | CACTCCAGCCTAGGC[A/G]ACAGAGCAAAACTGT | 84669 |
rs750184028 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60319892 | ATGATTTAAAGTATA[C/T]GGGGGTGAGGGGTGT | 84669 |
rs750201668 | snp | C/T | 2.53997e-05 | 0.0035636 | intron-variant | USP32 | GRCh38.p7 | 17:60208613 | TTTAAATAAAGTAAA[C/T]TTAATGGAGTCAAGT | 84669 |
rs750223272 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60422462 | TGTGTTGGCGGTTGC[C/G]GTGGCTTTGCTCCGA | 84669 |
rs750229080 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60271191 | GAATATCAGGCTCAA[C/G]ACTATAATAATAATT | 84669 |
rs750245177 | snp | C/T | 1.72555e-05 | 0.00293725 | intron-variant | USP32 | GRCh38.p7 | 17:60208851 | TAAAAAAGATGAGAA[C/T]TTTCTCTCAAAATCC | 84669 |
rs750252631 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60196096 | ACATGGTGAAACCCT[A/G]TCTCTACTAAAAATA | 84669 |
rs750257473 | in-del | -/CTTT | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406813 | GCCACTGCGCCTGGC[-/CTTT]CTTTCTTTCTTTCTT | 84669 |
rs750277088 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60207786 | TTTGGTGGAAACCTA[C/T]ACTATAGTGACACAG | 84669 |
rs750281654 | snp | A/C | 1.66322e-05 | 0.00288371 | intron-variant | USP32 | GRCh38.p7 | 17:60271497 | CTAAGGGTCAAATCA[A/C]AAAAGATTATAAAAC | 84669 |
rs750282769 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60262791 | CTTCTATTCTACCCC[-/T]AGTTGTTACCTCTTT | 84669 |
rs750285309 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60318257 | AGCATATATAAAGAT[A/G]TAGAAGAAGATCAAG | 84669 |
rs750294542 | snp | A/G | 0.000610936 | 0.017467 | intron-variant | USP32 | GRCh38.p7 | 17:60213564 | ATTTAATATAGATGC[A/G]TGCTTCCATCTTGTA | 84669 |
rs750307720 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60362370 | CAAATGGAGAAATAC[A/G]CAAGTTGGATGGGTT | 84669 |
rs750308890 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60185922 | AATCTAAAAATTAGC[G/T]GGGCATTGTGGTACA | 84669 |
rs750315307 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60374884 | ATCATCATGCAGCAC[-/A]ATGACTGTATAGGTA | 84669 |
rs750317481 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60292652 | TCACTGCTACACCAT[A/G]TTCTAAATGACTGAT | 84669 |
rs750323866 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60284295 | CTTGGCTCACTGCAA[-/C]CCCCGCCTCCCAGGT | 84669 |
rs750331338 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406536 | TTTTCTCTTTTTTGA[A/G]ACAGAGACTTGCTCT | 84669 |
rs750345039 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60307718 | ACCCTCAGGCCTGTG[C/T]CCACAGACCTAGGTG | 84669 |
rs750355600 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60247547 | GTTTCATTCTTCTGC[A/C]CGTGGATATCCAATT | 84669 |
rs750393341 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181423 | AAGCTGACCATTGCT[A/G]TAGCCATTGCCACAT | 84669 |
rs750395854 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | USP32 | GRCh38.p7 | 17:60226080 | GATGCAGTAGAAATG[C/T]TGTCTGAAAATTTCT | 84669 |
rs750404896 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378534 | CAATAGCCAAAAGGT[G/T]GAAACAACTCAAATA | 84669 |
rs750425321 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60254326 | CCTTCCCACTTAATC[C/T]TTTTTGGACCTTCTA | 84669 |
rs750431305 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | USP32 | GRCh38.p7 | 17:60198318 | TCGCTAACCGGGATA[C/T]TTGAATCCAAACCGC | 84669 |
rs750433328 | snp | G/T | 1.67562e-05 | 0.00289444 | intron-variant | USP32 | GRCh38.p7 | 17:60205429 | GACTGGCAGTGAGTT[G/T]CCTAACATTTAACTA | 84669 |
rs750435828 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377734 | TTAATTTATCCACAG[A/G]CTGTGTGAATAATTT | 84669 |
rs750446877 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60193785 | AGGGCAAAGGTGAGA[A/T]TCACATCTGGCATAG | 84669 |
rs750464514 | snp | C/T | 1.65304e-05 | 0.00287488 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269494 | CAACAGGCTGATAAC[C/T]CACAGGATATCTCCT | 84669 |
rs750478833 | snp | C/T | 1.79625e-05 | 0.00299682 | intron-variant | USP32 | GRCh38.p7 | 17:60183129 | TAGCCTACAGGAGTC[C/T]CAAGAAAGCACCTGC | 84669 |
rs750491730 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60192351 | GTAATAAATGTTTAT[C/T]ACAAGCTATGAATTT | 84669 |
rs750492845 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60222852 | ATGCCCGGCTAATTT[C/T]TGTATTTTTAGTAGA | 84669 |
rs750521958 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353770 | ATAATTTAGATAATC[C/T]ATGTAAATCGCTTTT | 84669 |
rs750543905 | in-del | -/GG | 6.36747e-05 | 0.0056421 | intron-variant | USP32 | GRCh38.p7 | 17:60252334 | AGTAACCAATATATT[-/GG]TCAAGTATGTGAAAT | 84669 |
rs750568674 | snp | A/G | 8.49322e-05 | 0.00651605 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391965 | TCCCCTCGGCGGGGG[A/G]TCGGAGCCTGATCTC | 84669 |
rs750569920 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60374664 | AGGTGGGAGCCACCA[C/T]GTTCAGCCAACTTTT | 84669 |
rs750570420 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60330273 | TCTTTGCTGTTCTAC[A/G]CTTTTCATCCATGAT | 84669 |
rs750586215 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60196278 | CCACGCCAAAAAAAG[-/AA]AAAAAAAAAAAAGAA | 84669 |
rs750604929 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60304358 | TGCTTCCCTTTATTT[C/T]TTTATTTTTTTTTTT | 84669 |
rs750608453 | snp | C/T | 1.67545e-05 | 0.0028943 | splice-donor-variant, intron-variant | USP32 | GRCh38.p7 | 17:60391881 | ACCCCTCCCCCCTCA[C/T]CTCTCCTCAGCGCCT | 84669 |
rs750622120 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60386470 | AAAACAGATTTTTCT[C/G]TAGTGACAACAAAAA | 84669 |
rs750632126 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60234861 | AGATTACAGGCCCAG[A/C]CAGACTTCATTCTTA | 84669 |
rs750638357 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60263318 | ACTATCCAAGGGTAA[C/T]ATCTAGATCTCTTGA | 84669 |
rs750639040 | in-del | -/TATC | | | intron-variant | USP32 | GRCh38.p7 | 17:60246429 | TTTTTTTTTTTTCTT[-/TATC]CATTCATCAACTGAT | 84669 |
rs750646846 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60402004 | CATGGGCAACCTTTC[G/T]GGAAAAGGGTGCTAA | 84669 |
rs750654077 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | USP32 | GRCh38.p7 | 17:60183309 | GCTCATCCCCCTGGG[A/G]TGTGAGTGGTTTATG | 84669 |
rs750659483 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60302898 | CAACAGAAATCACAA[G/T]AAATTCACTCATTCA | 84669 |
rs750705422 | snp | C/T | 1.65512e-05 | 0.00287669 | intron-variant | USP32 | GRCh38.p7 | 17:60180499 | TGTTCCCCAGTTCTG[C/T]TGATATTCTGTTTCT | 84669 |
rs750718305 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60349998 | GCTCTGTGGTTTTTT[C/T]GTTGTTGTTGGTTTT | 84669 |
rs750735448 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60387676 | GATACAACTTACAAT[C/G]AGATTACCTCCCAAT | 84669 |
rs750746500 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60329368 | CCCACAGAATTGTTG[A/G]CTATTATATGCTAGG | 84669 |
rs750773816 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60290205 | CGCCCACCAACTGAA[G/T]TTTGCCAGCTCCCTA | 84669 |
rs750780944 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60236335 | TTATAAGGAAAACCG[C/T]GAAACATTTAGATGT | 84669 |
rs750795444 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60340561 | TTTGAGCCTATGTAC[A/G]ACTTTGCACGTGAGA | 84669 |
rs750811780 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60386616 | CTCTAACTTCCTTAC[A/G]CATCTTTCTGGAAGG | 84669 |
rs750820136 | snp | A/C/G | 3.3184e-05 | 0.00407319 | missense | USP32 | GRCh38.p7 | 17:60214741 | GTATAGGCTAATACC[A/C/G]GCTTTAAAGGTGCAT | 84669 |
rs750829129 | snp | A/G | 1.64885e-05 | 0.00287123 | intron-variant | USP32 | GRCh38.p7 | 17:60180647 | ATGGCACTGTAAGAG[A/G]TAAGAGAGTGGAGGT | 84669 |
rs750838827 | in-del | -/GT | | | intron-variant | USP32 | GRCh38.p7 | 17:60294385 | GGTTCCTGCAGGAGT[-/GT]GTGTGTGTGTGTGTG | 84669 |
rs750848462 | in-del | -/AAAAAAAAAA | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407782 | GCAAGCCTCTGTCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 84669 |
rs750881038 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60296770 | AGGACACCAAAATCT[G/T]CAGGTGCTCAAGCCT | 84669 |
rs750884006 | in-del | -/CTG | | | intron-variant | USP32 | GRCh38.p7 | 17:60362220 | TAGTCTGAGAAAATT[-/CTG]CTCTTTTCTAACAGA | 84669 |
rs750886074 | snp | A/G | 3.43306e-05 | 0.00414296 | intron-variant | USP32 | GRCh38.p7 | 17:60211145 | AGAGGAAAATTTGTT[A/G]CCAAAGATTCTCATA | 84669 |
rs750890980 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60259223 | AGGAAACACTGAGAA[A/G]ATAAAGACCAACCTG | 84669 |
rs750925187 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60187524 | GGGGTGTATCATATA[C/T]GGTAGTGTTTCCTTT | 84669 |
rs750934011 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60222122 | CTGAACTTTTTGGCA[C/T]TGGCTCTTGGCCTGT | 84669 |
rs750937054 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409757 | TCCAATCTTTTGGCT[G/T]CCCTGGGTCACATTG | 84669 |
rs750939438 | snp | A/G | 3.32276e-05 | 0.00407586 | intron-variant | USP32 | GRCh38.p7 | 17:60271305 | ATGAGATGGGCTCAG[A/G]TATGTTTACCAGTGA | 84669 |
rs750941868 | snp | C/T | 1.77666e-05 | 0.00298043 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231551 | CAAGGCTGCCCCACT[C/T]GTGGCAGTCCTGACG | 84669 |
rs750954199 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | USP32 | GRCh38.p7 | 17:60198442 | ATACAGTTCTGTCCT[C/T]ATCTGTATGTACAAA | 84669 |
rs750962750 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60369702 | TACTTGCAGCAAATT[A/G]GTGAAATAGTTGATT | 84669 |
rs750973228 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60310392 | GGTATATACACACAA[C/T]GGAACATTATTCAGC | 84669 |
rs750974053 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232275 | CTTCTTGGGTTTAAG[C/T]GATTCTCCTGCCTCA | 84669 |
rs750978280 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60275585 | TAGTACCAGACATGA[C/T]CTTGGCATCTAGTAA | 84669 |
rs750982956 | snp | A/G | 1.66236e-05 | 0.00288297 | missense | USP32 | GRCh38.p7 | 17:60211406 | AGATGTCTCCCTGAG[A/G]TAAAATACTGTGTCA | 84669 |
rs750993559 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60383326 | CATATAGTATAACTC[A/G]ATTCCTGTCTTTATT | 84669 |
rs751033236 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60395035 | AGGCACGAGCCACCA[C/T]GCCTGGGCTACAGTA | 84669 |
rs751036783 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60400020 | TTGACCCTGGAGTGC[A/G]GTAGTGTGATCTCGG | 84669 |
rs751040153 | snp | C/T | 1.65138e-05 | 0.00287343 | missense | USP32 | GRCh38.p7 | 17:60205658 | GGCGAAGAGGAGAAA[C/T]CTACAAATTCAAAGA | 84669 |
rs751043214 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60398369 | CACTGCACTCAAGCC[C/T]GGGCAACAGAGTGAG | 84669 |
rs751051922 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60196402 | CTTCACTTCAAATTT[A/C]ATCTTGTCCAACTTT | 84669 |
rs751058892 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60337835 | ACAATGAGCCATGAT[C/T]GGGCCACTGCACTCC | 84669 |
rs751058904 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60318812 | TAGCAAGATACAAAA[A/T]CGGTAACCTTGTAAG | 84669 |
rs751088592 | snp | C/T | 4.94662e-05 | 0.00497299 | missense | USP32 | GRCh38.p7 | 17:60226189 | ATGAGTATTTTCCTC[C/T]ATTCAAAACAGATGA | 84669 |
rs751096511 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | USP32 | GRCh38.p7 | 17:60226097 | GTCTGAAAATTTCTC[C/T]TCTGTAGTATTCACG | 84669 |
rs751100709 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377978 | CCATGAAAGACAATC[-/CA]CAGATATTAATATAT | 84669 |
rs751127156 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60254710 | TCTCAAAATTAAAAA[C/T]AATAATGATAATAAT | 84669 |
rs751141086 | snp | A/G | 1.65321e-05 | 0.00287502 | missense | USP32 | GRCh38.p7 | 17:60207050 | CTAGAAGCTGAAATT[A/G]GAGACACAGGGACAG | 84669 |
rs751177922 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60272475 | CGTACATAGGACATT[G/T]ATTCTCAACTAAACA | 84669 |
rs751193414 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60219562 | AACGTAGTTTTCACC[-/T]TTTTTTTTTTTTTTT | 84669 |
rs751200149 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60385110 | GATGACATTCCACCA[C/T]TGTGATTTATTCCTG | 84669 |
rs751218015 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60320217 | ACAGGTTAATTGATA[A/T]AAACAAGAGTCAAGT | 84669 |
rs751222828 | snp | A/C | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423608 | AGATGGGATTACAGG[A/C]ACGTGCCACCACACT | 84669 |
rs751235730 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60364706 | ATTTAACATTCATGA[A/G]TTTACAATCATTTAC | 84669 |
rs751244653 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60203826 | ACGATCCACCCGCTT[C/T]GGCCTCCCAAAGTGC | 84669 |
rs751266596 | snp | G/T | 1.67697e-05 | 0.00289561 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265493 | TAAAAATAACCCAAA[G/T]GAGTAATTAGAAAAC | 84669 |
rs751280267 | snp | A/T | 1.68004e-05 | 0.00289826 | missense | USP32 | GRCh38.p7 | 17:60252416 | TTCCGGAGTAGCTGG[A/T]CTTAACCCCAGAACT | 84669 |
rs751324294 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242698 | AGGCATGAGCCACCA[C/T]GCCTGGCCAAGGGTT | 84669 |
rs751324478 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308972 | ATCTTTCAGCATACA[C/G]AAAAAATCAAATCAA | 84669 |
rs751332802 | snp | A/T | 1.67047e-05 | 0.00288999 | intron-variant | USP32 | GRCh38.p7 | 17:60192954 | GAAGAGAACAAAAAG[A/T]GTGTAAGAAGCATTT | 84669 |
rs751356626 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60185021 | GTGTGCTTGTGTACA[C/T]ACACTCAACTCAGTA | 84669 |
rs751363625 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60292753 | CAGCCTACTTCCCAC[A/G]TAAGATCCAAAGTGA | 84669 |
rs751366270 | snp | C/G | 3.30579e-05 | 0.00406544 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60294737 | ATCCACCACGTGGAG[C/G]ATTCTTTCCATTTCT | 84669 |
rs751376140 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60255998 | CAGAATCACTGAAGT[A/G]TATAGATCAACTGTC | 84669 |
rs751418639 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60309085 | TTCTGGGGAAAAAAA[A/T]TTTTGTGTAATACTT | 84669 |
rs751421100 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181522 | TTGGCTGCCCCCCAG[C/T]ACATGCCCTCGACTC | 84669 |
rs751449820 | snp | C/G | 1.71053e-05 | 0.00292444 | missense | USP32 | GRCh38.p7 | 17:60181647 | TCTGGGGCAGCCGGA[C/G]CCTCCCTTTGCTCCT | 84669 |
rs751463417 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60225823 | GCCAGGCGTGGTGGC[A/G]GGTGCCTGTAATCGC | 84669 |
rs751465417 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60241852 | AATGCTCTCTCTTGA[A/C]ACTCAAACGTTTTTA | 84669 |
rs751477865 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393570 | GTAACCATTTGGATT[A/C]GATTGGACCCAAGGT | 84669 |
rs751483897 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60245589 | AACTGGTGCTGGATG[-/A]AATTCTTGGTTCTCT | 84669 |
rs751499252 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60294188 | TTGGATTACAGGTGT[A/G]AGCCACCTTGCCTGG | 84669 |
rs751515709 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60372024 | ATCTAAAATTACCAT[A/G]TAACTATTGCGGTAG | 84669 |
rs751516915 | snp | A/T | 5.52685e-05 | 0.00525654 | intron-variant | USP32 | GRCh38.p7 | 17:60288690 | TTTTCACCCTAAAAT[A/T]AAAACAAGAAAACAT | 84669 |
rs751543719 | snp | A/T | 1.66145e-05 | 0.00288218 | missense | USP32 | GRCh38.p7 | 17:60214646 | ATAGCCACAGGCGCA[A/T]ATCTTCCTCTTTAAT | 84669 |
rs751557802 | in-del | -/C | 5.43198e-05 | 0.00521123 | intron-variant | USP32 | GRCh38.p7 | 17:60255306 | TTTTTTCTTTTTTTT[-/C]TTTTTTTTTGAGACG | 84669 |
rs751561395 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405337 | CCTCCCAAGTAGCTG[G/T]GATTACAGGCACACA | 84669 |
rs751581909 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60348901 | GAACCACTAGTTGAA[C/T]AAGTAGCTAGAGAAA | 84669 |
rs751626064 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60304377 | ATTTTTTTTTTTTAC[A/G]GAAACAAAAACAGAG | 84669 |
rs751627842 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60255858 | AACTAAATCAACAAA[C/G]ATGTTCTGGTAACAT | 84669 |
rs751664643 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60268490 | GGATGGGAGGATCCA[C/T]TGAGCCCAGAAGTTC | 84669 |
rs751665422 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60289538 | ATGTACACAGAGAAC[-/A]AAAAGAAGCAAGTTG | 84669 |
rs751693738 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290982 | TACCAAATGTTTACA[A/G]TGTCCTAAGAACTGC | 84669 |
rs751696277 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60250995 | TCACCCAGGCTGGAA[C/T]GCAATGGCATAATCT | 84669 |
rs751707132 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360341 | TATTTTTTGTATTTT[C/T]ACAAATACAAAAAAT | 84669 |
rs751707277 | snp | C/T | 2.57921e-05 | 0.00359102 | intron-variant | USP32 | GRCh38.p7 | 17:60208623 | GTAAATTTAATGGAG[C/T]CAAGTAATTTTTCAG | 84669 |
rs751730800 | snp | A/G | 1.65551e-05 | 0.00287702 | synonymous-codon, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269514 | GGATATCTCCTTAAA[A/G]TCTATGTGATTGTCA | 84669 |
rs751741929 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60275734 | ATTTTTTTTCCAAGA[C/T]GGAATCTCACTCTGT | 84669 |
rs751796466 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404972 | TCTTGAGGTGAGGAA[C/T]TGGAGACCAGTCTGG | 84669 |
rs751796868 | snp | A/C | 1.74631e-05 | 0.00295487 | intron-variant | USP32 | GRCh38.p7 | 17:60208872 | CTCAAAATCCAAAAG[A/C]GAAGCATTTCTATAT | 84669 |
rs751798546 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60387971 | AAGTTAAATTGTAAG[C/T]CGGGGATTGTCTATA | 84669 |
rs751806083 | in-del | -/AATT | | | intron-variant | USP32 | GRCh38.p7 | 17:60191999 | AGAACTGGCAAACTT[-/AATT]ATATTTAACGAGAGG | 84669 |
rs751813473 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60342711 | AGTGAGCAAGGCTCC[A/G]TGGGCATGGGACCCG | 84669 |
rs751830316 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60293093 | AGTTATCTGATAGAC[C/T]TAAGCATTCTATATA | 84669 |
rs751843015 | snp | A/G | 3.30371e-05 | 0.00406417 | synonymous-codon | USP32 | GRCh38.p7 | 17:60211438 | TGGCTGTGTGTTACT[A/G]ACACACTGGATGCTT | 84669 |
rs751847263 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60234730 | AGCAAGACTCCGTCT[C/T]AGAAAAAAAAAAATT | 84669 |
rs751856958 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60290401 | TGTTGCAGGGACATA[A/T]GAGTACACTGCCAAC | 84669 |
rs751872551 | snp | C/G | 1.64762e-05 | 0.00287016 | missense | USP32 | GRCh38.p7 | 17:60181382 | TCTCTTTGGTCATCA[C/G]TGCTGTCTTCTTCAC | 84669 |
rs751874853 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411484 | TACCATTACACTCTA[A/G]CCTCGGTGACAAAGT | 84669 |
rs751888217 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60252555 | CAGTTTTCAACTCAT[A/G]AATTATCAATTATTC | 84669 |
rs751890479 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60222339 | GGTTAGTGAGAGTCA[C/T]ATAGAAAAAGTAACA | 84669 |
rs751896184 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418110 | ATTATAGGCATGTGC[C/T]ACCACGCCCAGCTAA | 84669 |
rs751909888 | snp | C/T | 4.94442e-05 | 0.00497188 | missense | USP32 | GRCh38.p7 | 17:60345590 | GCATCCTTCAGTCGT[C/T]TTAGCTCTACATCTG | 84669 |
rs751925469 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60369773 | TTTAAGAGACAGGTT[C/T]TTGCTGTCACCCAGG | 84669 |
rs751934240 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60277392 | AAACAACCTCCTCTC[A/G]GGAGCAATGACCTTC | 84669 |
rs751938744 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60184670 | AAAAATTAGCCGGGT[A/G]GTAGTGGTGCATGCC | 84669 |
rs752027110 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60389183 | GAAACCAATGAATGC[A/T]GGTTTTACCAACTGT | 84669 |
rs752029999 | in-del | -/TG | | | intron-variant | USP32 | GRCh38.p7 | 17:60342112 | TGTCCTTTTTGTTGA[-/TG]ATGATGCTATTCCTT | 84669 |
rs752031126 | snp | G/T | 1.67871e-05 | 0.00289711 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205455 | AACTAACCATTTTTC[G/T]GTGGACTGCAATGAT | 84669 |
rs752090915 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60199568 | GAGTAGTTAGAAAAG[C/T]TAAATCAACAACTTA | 84669 |
rs752103952 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60362244 | TCTAACAGAAAGTTC[A/G]TATTAACAAGCATAA | 84669 |
rs752115252 | snp | C/T | 3.30213e-05 | 0.00406319 | missense | USP32 | GRCh38.p7 | 17:60185603 | CCAGGTTGATGGGCT[C/T]GGCTTGCGCTCGCCG | 84669 |
rs752118860 | snp | C/T | 4.94303e-05 | 0.00497119 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183238 | GTCCTCTTCCCCAGC[C/T]GAACTCTGCGCATCC | 84669 |
rs752119921 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312440 | TGTCGTTGTCGTTGT[C/T]GTTGAGACAGGGTCT | 84669 |
rs752123017 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | USP32 | GRCh38.p7 | 17:60205566 | ATGGCACAACAGTGT[C/T]TGGCATTCCATTGGG | 84669 |
rs752140184 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232259 | CTCACTGCAACCTCT[C/G]CTTCTTGGGTTTAAG | 84669 |
rs752141653 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60272844 | TGGAGAGGAAAGAGT[C/T]ATGCCAAGAAAGGGC | 84669 |
rs752143956 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60321764 | TCCCTAAATCTATCA[A/G]TTGGAAATCTGGAAA | 84669 |
rs752195102 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60338749 | AAAACATAGTGGCCT[C/T]GGTTCAGAAAAAGAC | 84669 |
rs752237332 | snp | A/T | 0.000166995 | 0.00913617 | missense | USP32 | GRCh38.p7 | 17:60214715 | TGGTCTGCATTCGAC[A/T]AAAACAGCCTGTATA | 84669 |
rs752257665 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60385188 | TCAGAAGCTCCCCCA[C/G]TGGGCACCTCGTGAC | 84669 |
rs752268651 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60240980 | CTGGTAGCCCCAGAC[A/G]GTTTAGACAAACACA | 84669 |
rs752281958 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60294433 | GTTAGTGTGAGTATA[C/T]AGAATTGTGTTTCAT | 84669 |
rs752285429 | snp | C/T | 0.000183216 | 0.00956945 | intron-variant | USP32 | GRCh38.p7 | 17:60198250 | GTTTAGATGGATCCC[C/T]TGAACTCACCAATCC | 84669 |
rs752288317 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60281876 | ATCAAAATCTTTGCC[A/G]ACAGAGCCAGTAACC | 84669 |
rs752291484 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60203290 | CCTGTAGTATCAGCT[A/G]CTTGGGAGGCTGAGG | 84669 |
rs752291997 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60239500 | GTTCTGTTCATTTTT[C/T]GTCATTCTGTTTTCT | 84669 |
rs752299758 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60320623 | AGTGGCCCTGGCCAG[A/T]AATTGATGTTTTTTT | 84669 |
rs752304566 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309956 | GTCTGAGGCAGGAGA[A/G]CTGTTTGAACCTGGG | 84669 |
rs752306118 | snp | A/C | 1.66813e-05 | 0.00288797 | intron-variant | USP32 | GRCh38.p7 | 17:60190531 | ATTTCTCATATAAAA[A/C]CCACCATTTTATGGT | 84669 |
rs752319678 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60347018 | CAGACGAGAAAAAAA[C/G]ACAGTGAGATATAAT | 84669 |
rs752327283 | snp | C/T | 1.6686e-05 | 0.00288838 | missense | USP32 | GRCh38.p7 | 17:60214661 | TATCTTCCTCTTTAA[C/T]GCGCAGCCTTTGAGA | 84669 |
rs752340598 | in-del | -/GTACAAATTGT | | | intron-variant | USP32 | GRCh38.p7 | 17:60318071 | TTTTTAAAATCAGTG[-/GTACAAATTGT]GACATAGAAAGCATG | 84669 |
rs752351340 | snp | G/T | 1.65021e-05 | 0.00287241 | intron-variant | USP32 | GRCh38.p7 | 17:60180661 | GATAAGAGAGTGGAG[G/T]TATGTTAGCAGTTAA | 84669 |
rs752357817 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309131 | CAAAAGCAAAAATAG[A/G]CAAATGGGATTTGAT | 84669 |
rs752360831 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60256181 | CATCTCTTTGAAAAA[A/C]AAAATAATAAAAATA | 84669 |
rs752397108 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60185253 | TGATTGATCTTCTAG[G/T]TTATAAGCTCTTTAG | 84669 |
rs752407925 | snp | A/G | 3.29728e-05 | 0.00406021 | missense | USP32 | GRCh38.p7 | 17:60223484 | TTAAGGTGCAACAAA[A/G]TATTCCCATTGGCTC | 84669 |
rs752417298 | snp | A/T | 1.65312e-05 | 0.00287495 | missense | USP32 | GRCh38.p7 | 17:60226204 | CATTCAAAACAGATG[A/T]TGGCTCAATTACCAC | 84669 |
rs752429406 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60228222 | TAGAGACAGGGTTTC[A/G]CCATGCTGGCCTCAA | 84669 |
rs752479310 | snp | A/T | 1.92792e-05 | 0.00310471 | intron-variant | USP32 | GRCh38.p7 | 17:60181794 | AATTCAAATGCCACA[A/T]AGTAAGCCAGCCCCA | 84669 |
rs752488963 | snp | C/G | 1.70278e-05 | 0.00291781 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391968 | CCTCGGCGGGGGGTC[C/G]GAGCCTGATCTCGCC | 84669 |
rs752519600 | in-del | -/GTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60397363 | ATCAGGCTTTTTCCA[-/GTT]GTTGTTGTTGTTTAA | 84669 |
rs752528324 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60303151 | GGAAATAGCTACAGA[A/C]CATTAAAAGTATTTT | 84669 |
rs752529805 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60330821 | CATAAGGAAAAGACA[C/G]AGTTCCAAATTTATC | 84669 |
rs752535152 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60315843 | TAGCATGGCCTGTAC[A/C]AAACAGATTGCCTGC | 84669 |
rs752549181 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393760 | CGCGATCTCGACTCA[C/T]CGCAACCTCTGCCTC | 84669 |
rs752550250 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409325 | AGCATTCCAGCCTAT[A/G]CAACAGAGCGAGACT | 84669 |
rs752551957 | snp | A/T | 1.64972e-05 | 0.00287199 | missense | USP32 | GRCh38.p7 | 17:60255250 | GTCTTCCAGAGTAAG[A/T]TGACCCATCTGAAAC | 84669 |
rs752552612 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377847 | CTGTGGGGTCACTCT[A/T]TCAGAATTTCATGGT | 84669 |
rs752567769 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60242109 | AAATTCTCCTGCACC[A/G]TTTTTTGTTTTTTAA | 84669 |
rs752572597 | in-del | -/A | 3.74167e-05 | 0.00432516 | intron-variant | USP32 | GRCh38.p7 | 17:60269421 | CTCTACATAGTTTGC[-/A]ATTTTTTGACAATGT | 84669 |
rs752581771 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60349925 | GTGAAATGTTGAAAA[C/T]TTTGAAAATAAAAAT | 84669 |
rs752601060 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60229569 | GTCATTTGCTTCCTG[C/T]CCATAAAGATGGAGC | 84669 |
rs752620402 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283062 | ATGCAAATAGTAAAA[C/T]AAATTAACTCAAAGA | 84669 |
rs752626541 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60313109 | TACAAAAATTAGCCA[-/G]TCATGGTGGCAGGCA | 84669 |
rs752641571 | snp | A/G | 1.68641e-05 | 0.00290375 | intron-variant | USP32 | GRCh38.p7 | 17:60252447 | ATGTGACACACCTAG[A/G]GAAAAAAATGGTAAA | 84669 |
rs752683254 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60332625 | TGCACTCCAGCCTGG[A/G]CAACAAGAGAGAAAC | 84669 |
rs752687260 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60315357 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCACA | 84669 |
rs752691927 | snp | C/T | 1.64972e-05 | 0.00287199 | intron-variant | USP32 | GRCh38.p7 | 17:60236266 | AAAAGAAATTAAATA[C/T]ATCAAACAAAGTGTG | 84669 |
rs752746770 | in-del | -/AAAT | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411328 | AACTGTCTCAAAAAT[-/AAAT]AAATAAATAAATAAA | 84669 |
rs752756276 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60344891 | CTGGACTCGAGTTCT[G/T]GGGCTTAAGCAAGCC | 84669 |
rs752758404 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60326298 | CCTTATTTGACACCA[C/T]GGTTTGTTTTCTTTT | 84669 |
rs752773156 | snp | C/T | 1.68117e-05 | 0.00289923 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179234 | TCACCGCCAAGCTGT[C/T]TAGCAGCCAGAGTGG | 84669 |
rs752780001 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60389792 | GAGGCCGAGGCGGGC[A/G]GATCACAAGGTCAGG | 84669 |
rs752794702 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | USP32 | GRCh38.p7 | 17:60219688 | TATTCACCCAGATGT[C/T]AGACTGCTGTGTCCG | 84669 |
rs752811564 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60342839 | TCTGACATGGATTCC[C/T]GTGGCTAGGAAAGGG | 84669 |
rs752812219 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60312651 | CTTACTATGTTGCCC[A/G]GGCTAAAAAATTTAT | 84669 |
rs752817553 | in-del | -/GCAGAAGAATC | | | intron-variant | USP32 | GRCh38.p7 | 17:60275361 | ACTCAGGAGGCTGAG[-/GCAGAAGAATC]GCTTGAACCTGGGAG | 84669 |
rs752823629 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60179694 | TTTATTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 84669 |
rs752833494 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405111 | TAGAGGCTGCAGTGA[C/T]CCACGATCATGCCAC | 84669 |
rs752837117 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60391522 | TTTATGAAGGAATGA[C/T]AGGAGAAAATGGCAA | 84669 |
rs752840266 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413372 | AGCTCATACTTAAGA[A/C]CTGACCTCCCAGATG | 84669 |
rs752868802 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60261217 | TAGTGTAAACCCATT[G/T]TAATTTTATAGGACT | 84669 |
rs752902560 | in-del | -/AGGCCCCC | 1.76643e-05 | 0.00297184 | intron-variant | USP32 | GRCh38.p7 | 17:60183148 | GAAAGCACCTGCATA[-/AGGCCCCC]AGGCCTCACCTTTCG | 84669 |
rs752936772 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60224060 | TTGTATCTATGAACT[C/T]AATGTCCACAAGTTC | 84669 |
rs752943992 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60340974 | TTGAAAATTCTTTTC[-/T]TTTAAGAATGTTGAA | 84669 |
rs752946362 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60184238 | GAGAATGGCATGAAC[A/C]CAGGAGGTGAGGCTT | 84669 |
rs752952266 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60321872 | TTTTAATCAGATGGC[-/T]TTTTTTTTTTTTTAG | 84669 |
rs752969880 | snp | C/T | 3.29478e-05 | 0.00405867 | missense | USP32 | GRCh38.p7 | 17:60205577 | GTGTTTGGCATTCCA[C/T]TGGGGATGAATATTG | 84669 |
rs752976131 | in-del | -/TAAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60267484 | CCTTTCCAGTATAAC[-/TAAT]GTACATTCAATCTTT | 84669 |
rs753002246 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60300027 | CCCCTAATACCATCA[C/T]CTTGGTGGTTAGGAT | 84669 |
rs753004626 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413182 | TGGAGAGATGCTCAT[A/G]ACTTATGTGCAGAGA | 84669 |
rs753011474 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60398694 | AGCTAGGTACAGTGG[C/G]TGGCTCAGAAATTAA | 84669 |
rs753028418 | snp | C/T | 9.92113e-05 | 0.00704243 | intron-variant | USP32 | GRCh38.p7 | 17:60222581 | TGACAATGTTGACTT[C/T]CAATATTACAAAAGT | 84669 |
rs753044816 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191970 | GTCTAGTAAAGACTA[C/T]GGTCTACTGTGCTTA | 84669 |
rs753049081 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60356107 | CTCATTAAAAAGTTC[C/T]ATTCTCAAGCTTTGT | 84669 |
rs753059819 | snp | C/T | 1.65655e-05 | 0.00287793 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265933 | CCCTCCAATTTCCCA[C/T]TGGAAGTTTATACGC | 84669 |
rs753072303 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60313822 | GCTAGAATAAAATCC[A/G]ACATTTTAAAAACAA | 84669 |
rs753072481 | snp | C/T | 4.94271e-05 | 0.00497102 | missense, utr-variant-5-prime, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266035 | CAACCACCATGTCTC[C/T]CAGTTCAACCCTGGA | 84669 |
rs753072825 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60262846 | CTTCTGTTAACCATA[A/T]TTAACTAATTATTAA | 84669 |
rs753078386 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60227707 | CGTGAGCCACTGTGC[A/C]CAGTGGACATAAGTT | 84669 |
rs753147497 | snp | A/T | 4.94784e-05 | 0.00497361 | missense | USP32 | GRCh38.p7 | 17:60345606 | TTAGCTCTACATCTG[A/T]AACTGCAATTCAGAA | 84669 |
rs753154998 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60391012 | CAGCGGTATCAGAGT[A/G]AGTGGTAGGGGGTTG | 84669 |
rs753162595 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60391862 | TCCCAGGCAGCTCGC[C/T]CAGACCCCTCCCCCC | 84669 |
rs753166336 | in-del | -/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412513 | CACTCCAGCTTGGGT[-/G]GACAGAGTGATACCC | 84669 |
rs753169758 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | USP32 | GRCh38.p7 | 17:60183332 | GGTTTATGCTGGCAG[A/G]GAGCCGGGTCTCTTG | 84669 |
rs753183802 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60373150 | GTAAGCCATGATCAC[A/G]CCACTTCAATCTACC | 84669 |
rs753183930 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353779 | ATAATCTATGTAAAT[C/T]GCTTTTACAAAGTCA | 84669 |
rs753189914 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60303449 | GAATGTCTTTGAGGT[A/G]TGATAACAAATAGAA | 84669 |
rs753220450 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60287432 | CTGAAAGTTACCCTT[A/G]CCTTTAAAAACCCTT | 84669 |
rs753223087 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60187439 | CTTTTGAACTGGTCA[C/T]TCAAGGAAAAAACTG | 84669 |
rs753226040 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232646 | CTGCCTCCTAGGTTC[A/G]AGCTATTCTTGTGTC | 84669 |
rs753257426 | snp | C/T | 1.67863e-05 | 0.00289704 | missense | USP32 | GRCh38.p7 | 17:60183419 | GATTTTATCCACCGA[C/T]CATTTACAAATTGAA | 84669 |
rs753272061 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60327568 | GTTGGGCAGGAGGGG[C/T]AGGCAGAGAGGGGCC | 84669 |
rs753276674 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60337964 | ATGTTGTGCTATGTA[C/T]TACAGATTCAGGCTT | 84669 |
rs753282302 | in-del | -/A | 1.66363e-05 | 0.00288407 | intron-variant | USP32 | GRCh38.p7 | 17:60288507 | AAACAGAAAACAATG[-/A]AATGTCATTACTTAC | 84669 |
rs753284054 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60357484 | ATATATATATGATAT[A/G]TAGACCAAGCAAGCA | 84669 |
rs753299323 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60301432 | TGTAATTTTAATTTA[C/T]ATTTCTCTAATGACT | 84669 |
rs753339760 | snp | A/C | 3.41291e-05 | 0.00413079 | missense | USP32 | GRCh38.p7 | 17:60301605 | AGTACTTACATTTTG[A/C]TTTCTCTTCATCTTT | 84669 |
rs753357135 | snp | C/T | 1.64958e-05 | 0.00287187 | synonymous-codon | USP32 | GRCh38.p7 | 17:60190683 | ACAGCCTCTGCAAAA[C/T]CTAAAAAGGGGGAAA | 84669 |
rs753384170 | in-del | -/AAAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60316844 | GACTTTGACTCATAA[-/AAAC]AAACAAACAAACAAA | 84669 |
rs753405307 | in-del | -/AAAAAAAA | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413877 | AAAAAAAAAAAAAAG[-/AAAAAAAA]AAAAAAAAAAAGAAT | 84669 |
rs753411555 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60185705 | AAGGCATTTAAAGTG[A/G]TGATCTAGGTATGCA | 84669 |
rs753416771 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60367720 | GGTTGGGGCATGAGA[A/C]TCACTTGAACCTGGG | 84669 |
rs753423241 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60312733 | AAAATATATACCTTT[A/C]CAAAGAACTTGATGT | 84669 |
rs753451700 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283260 | GTATATTGACCAGTG[C/T]TCTGTAGTTGAGGCA | 84669 |
rs753452315 | snp | C/T | 5.02727e-05 | 0.00501337 | missense | USP32 | GRCh38.p7 | 17:60212026 | ACTGGAGACTTACCC[C/T]TGTGTCTATCTATTT | 84669 |
rs753460365 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60331000 | AGTCATATACCTAAA[C/T]TCCTACAATTCTGAT | 84669 |
rs753460840 | snp | C/T | 1.6516e-05 | 0.00287362 | synonymous-codon | USP32 | GRCh38.p7 | 17:60211477 | GAAGCATGTGTTTCC[C/T]AGATTGCTTAGACCT | 84669 |
rs753462175 | in-del | -/GGCT | | | intron-variant | USP32 | GRCh38.p7 | 17:60344933 | CTCCTGAGTAGCTGG[-/GGCT]GACTACAGGGACGCA | 84669 |
rs753463059 | in-del | -/TAC | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60394330 | TTCAATTGCAACATA[-/TAC]TACTATTATTACTGT | 84669 |
rs753470915 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60274358 | GATCCCAGAAAGGGA[C/T]AGGCAGAAAAATATC | 84669 |
rs753496123 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60401578 | ATGATAATCAAGGGT[C/T]AAAAGTAGACCTCTG | 84669 |
rs753513602 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60380664 | TATTTTACATAGGAA[C/T]ACACATGTCAAATTA | 84669 |
rs753552787 | snp | C/T | 1.66338e-05 | 0.00288386 | missense | USP32 | GRCh38.p7 | 17:60214729 | CTAAAACAGCCTGTA[C/T]AGGCTAATACCCGCT | 84669 |
rs753555866 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60351470 | GATGGAGTCTCACTC[C/T]GTCCCCCAGGCTGGA | 84669 |
rs753565322 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60184210 | GTCCTAGCTACTCAG[A/G]AGGCTGAGGCAGGAG | 84669 |
rs753584880 | snp | A/G | 1.64912e-05 | 0.00287147 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183217 | TGGGCTTTTGCTCAG[A/G]AGCACGTCCTCTTCC | 84669 |
rs753609210 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60314036 | AATTTAAACAAAAAT[-/A]AAAAACATGGAAATA | 84669 |
rs753612798 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242309 | CTCCTGGACCATTTT[C/T]TTTTCTTTTTAAAGT | 84669 |
rs753613765 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60284130 | AAAAGAAAACAATCA[C/T]TAGGAATTAGAAGGT | 84669 |
rs753644992 | snp | A/T | 1.65274e-05 | 0.00287462 | intron-variant | USP32 | GRCh38.p7 | 17:60271340 | ATGTAGAAAATGGAA[A/T]GATCCCTACCTTCAC | 84669 |
rs753654150 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60290429 | AACATGTTTAGAGAT[G/T]AGAGTTCCTACCCAT | 84669 |
rs753670160 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60252797 | AAAACACTCAGCCAT[G/T]TGTGAGATCTTGGCA | 84669 |
rs753670657 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60218151 | CTTACCAAACAGGCC[A/G]AGGTGGATGGATCAC | 84669 |
rs753681827 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60266749 | CAACCTCTGCCTCCC[C/G]GGTTCAAGCAATTCT | 84669 |
rs753719168 | in-del | -/TTTC | | | intron-variant | USP32 | GRCh38.p7 | 17:60338901 | AGTACATAAAAATAT[-/TTTC]TTTGTTTCTTTCTTT | 84669 |
rs753731895 | snp | A/C/T | 3.33229e-05 | 0.00408173 | intron-variant | USP32 | GRCh38.p7 | 17:60190536 | TCATATAAAAACCAC[A/C/T]ATTTTATGGTGGCCC | 84669 |
rs753736037 | snp | G/T | 0.000107383 | 0.00732665 | missense, intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422607 | GATGGAGGCCTCAGA[G/T]GGGCAAGGGGGTGAA | 84669 |
rs753737859 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60362125 | ACCCCATCTTTGCAA[A/G]GCATCAGGTTGCCCC | 84669 |
rs753750813 | snp | A/C | 1.79133e-05 | 0.00299271 | missense | USP32 | GRCh38.p7 | 17:60208141 | AGCTGTTTTTTTAAA[A/C]CTGTGTACTTTTCAT | 84669 |
rs753769769 | snp | A/G | | | upstream-variant-2KB, intron-variant, synonymous-codon | C17orf64, USP32 | GRCh38.p7 | 17:60422319 | CCTGGCCTGCTGTGC[A/G]CTCTGCCAAAGTCTT | 84669 |
rs753775016 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60251945 | AGTAGGTATTTCAGA[A/T]TATTCCCATTTTTAT | 84669 |
rs753784374 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306403 | AGCACTTTGGAAAGC[A/C/T]GAGGGGGGTGGATCA | 84669 |
rs753790481 | snp | C/T | 0.000129537 | 0.00804685 | intron-variant | USP32 | GRCh38.p7 | 17:60255303 | TCTTTTTTTTCTTTT[C/T]TTTTTTTTTTTTGAG | 84669 |
rs753812817 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60269082 | ATTAATCTGTGCCAG[G/T]GGATGGAAAATGAGT | 84669 |
rs753830368 | snp | A/G | 1.72844e-05 | 0.00293971 | synonymous-codon | USP32 | GRCh38.p7 | 17:60211112 | CTTCATACCAATGGG[A/G]TTTGTCCTAGAAGTT | 84669 |
rs753838750 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305134 | TTTTGCATTGCTATA[A/G]AGGAATACCTGAGGC | 84669 |
rs753839181 | snp | C/T | 5.21435e-05 | 0.00510579 | intron-variant | USP32 | GRCh38.p7 | 17:60208253 | GTAAAATGCAGGTTT[C/T]ATTGAAAGTCTTAAA | 84669 |
rs753868123 | snp | C/G | 1.68491e-05 | 0.00290245 | intron-variant | USP32 | GRCh38.p7 | 17:60391873 | TCGCCCAGACCCCTC[C/G]CCCCTCACCTCTCCT | 84669 |
rs753890729 | in-del | -/AAAT | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411325 | GCAAAACTGTCTCAA[-/AAAT]AAATAAATAAATAAA | 84669 |
rs753897869 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60224504 | GAAATAATAACACAC[A/G]CCAGGAGGAATGGCT | 84669 |
rs753898944 | in-del | -/A | 6.73991e-05 | 0.00580474 | intron-variant | USP32 | GRCh38.p7 | 17:60211343 | TTATATCAAAGTCAC[-/A]GGTTAAGAGGCCAGT | 84669 |
rs753906758 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60312779 | TTAAAAGCCATCTTT[A/C]GGTAATGACAAAGAT | 84669 |
rs753918989 | in-del | -/C | 1.78646e-05 | 0.00298865 | intron-variant | USP32 | GRCh38.p7 | 17:60183476 | AGTAAAGGTAGAAAA[-/C]ATCTGCATTAAAGGG | 84669 |
rs753923586 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | USP32 | GRCh38.p7 | 17:60198311 | AGTGGGCTCGCTAAC[C/T]GGGATACTTGAATCC | 84669 |
rs753945916 | snp | G/T | 1.64779e-05 | 0.00287031 | synonymous-codon | USP32 | GRCh38.p7 | 17:60222535 | TCGTCCTCCTTCTAG[G/T]GTTAATGATGTAGCC | 84669 |
rs753950101 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60279679 | CCTTCTCTACAAAAA[A/T]TACAAAACTTAGCCA | 84669 |
rs753960406 | snp | G/T | 1.65138e-05 | 0.00287343 | intron-variant | USP32 | GRCh38.p7 | 17:60345630 | TTCAGAAACAGAAGA[G/T]GGGTAAGAAATCAGG | 84669 |
rs753962193 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60320021 | GCGTAAGTATCTTCA[A/G]TATCAGCATTGGAAC | 84669 |
rs753962327 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60282369 | ATACTCTTTTTTTTT[-/A]ATTGAGACGGGGTCT | 84669 |
rs753987585 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60240772 | TTTCCCAAGGAAACT[C/T]TCAAGTTCCCACCAC | 84669 |
rs753997793 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60301490 | TATTTACCACTTGTA[G/T]ATCTTCTTTGGGAAA | 84669 |
rs753998314 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60346301 | ATAGGCATACAAATT[G/T]TAGGCAGGGGCAAAG | 84669 |
rs754003137 | snp | A/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415436 | TTCCATGGGTTAAAG[A/T]CCCATCTAACTTCCA | 84669 |
rs754012578 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60391725 | CTGCTTCCCACCCGA[C/T]CTCTCTCCTCCACCA | 84669 |
rs754031421 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60374399 | TTACAGTTAAGTTTT[A/G]TTTTTTTTTTTTTGA | 84669 |
rs754040293 | snp | A/G | 1.65345e-05 | 0.00287524 | intron-variant | USP32 | GRCh38.p7 | 17:60222365 | TAACAGAAGACCCCC[A/G]TCTATGACTGCTCCT | 84669 |
rs754059383 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60225918 | GAGATCGCGCCACTG[C/T]GCTCCAGCCTGGGCA | 84669 |
rs754061283 | snp | A/G | 1.80286e-05 | 0.00300233 | intron-variant | USP32 | GRCh38.p7 | 17:60183120 | AAACATATGTAGCCT[A/G]CAGGAGTCCCAAGAA | 84669 |
rs754115244 | snp | A/G | 1.77253e-05 | 0.00297697 | intron-variant | USP32 | GRCh38.p7 | 17:60183468 | TCTGGAGAAGTAAAG[A/G]TAGAAAACATCTGCA | 84669 |
rs754119472 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60302990 | ATTAAACAATAATTC[A/G]AGAAGTTAGTCAATA | 84669 |
rs754132217 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60356706 | AGGGAATCCAATTTC[C/T]AGAGCTGCCACACTA | 84669 |
rs754137374 | in-del | -/AGA | | | intron-variant | USP32 | GRCh38.p7 | 17:60358711 | GAACATTATTCTTAC[-/AGA]AGGAGTTTATCATAG | 84669 |
rs754145986 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60287721 | GCAACCCTAGGAAAC[G/T]AATATAGCTTCATTA | 84669 |
rs754152851 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60281239 | GAGGATGCATATTCA[A/T]TATAAAACACATGCT | 84669 |
rs754158677 | in-del | -/AAAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60316845 | GACTTTGACTCATAA[-/AAAC]AAACAAACAAACAAA | 84669 |
rs754186490 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413093 | ATTAAATGGAAAACT[A/G]CAGTAAATATCAGAT | 84669 |
rs754195196 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403308 | GGCATGAGCCACTGC[A/G]CCCAGCCAAGCTGTA | 84669 |
rs754200698 | snp | A/G | 1.78096e-05 | 0.00298404 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231531 | ACATGTCTGAGGCAG[A/G]AAAACAAGGCTGCCC | 84669 |
rs754229841 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60362426 | CATTCTGAAACATGT[-/A]AAATATGCCACTATA | 84669 |
rs754243595 | snp | A/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416607 | CCAAAGGCAATGGAT[A/T]TTTGTTTTGTCTTAG | 84669 |
rs754255561 | snp | A/C | | | missense | USP32 | GRCh38.p7 | 17:60223527 | GGTTGTTATTGTCAG[A/C]AGTGTTATGTTGTCG | 84669 |
rs754263544 | snp | A/G | 1.65299e-05 | 0.00287483 | synonymous-codon, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269478 | AGCCAGGGGTCCCCT[A/G]CAACAGGCTGATAAC | 84669 |
rs754267796 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60184315 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs754278678 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | USP32 | GRCh38.p7 | 17:60185542 | CAGTAGTACATCTCA[C/T]TTTCCCCTAGCTCTT | 84669 |
rs754301987 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60193520 | ATCCTTGCCCTAACA[A/G]GGAGCAATGCAACAA | 84669 |
rs754302973 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60329373 | AGAATTGTTGACTAT[A/T]ATATGCTAGGTATGA | 84669 |
rs754305744 | snp | A/G | 4.94401e-05 | 0.00497168 | missense, utr-variant-5-prime, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266065 | AGAGAACTCCATCAC[A/G]GTCAACATCAAATAC | 84669 |
rs754316574 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60199767 | AGTACAAATATTTTA[C/T]AAAATTTTAAAACGT | 84669 |
rs754323086 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60386332 | TAATCTTCTCAGTAC[A/G]CTATCCAACTACTAA | 84669 |
rs754329547 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60274116 | AGAAATGGCAACTAT[A/C]AAGAAGTATCAACTG | 84669 |
rs754344911 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60323668 | TTCTTTTAAAGCAAA[C/G]AACTGGTGTATGTAA | 84669 |
rs754348710 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60272960 | ATGTACAAATGCCGG[A/G]AAATTTGTTTTGTTT | 84669 |
rs754349370 | snp | A/G/T | 0.000101744 | 0.00713181 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391960 | CCTCATCCCCTCGGC[A/G/T]GGGGGTCGGAGCCTG | 84669 |
rs754370249 | snp | C/T | 1.66913e-05 | 0.00288883 | intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179473 | AAGCCATCACTACTA[C/T]GGCTCTAAATCCTTG | 84669 |
rs754370319 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60322288 | GTAGCTGGGACTACA[C/T]GAACATACCACTATG | 84669 |
rs754390743 | snp | C/T | 1.73694e-05 | 0.00294693 | intron-variant | USP32 | GRCh38.p7 | 17:60209578 | CACAGTCATTATTTC[C/T]TACCCATAAAATTTG | 84669 |
rs754393495 | snp | C/T | 4.98625e-05 | 0.00499287 | missense | USP32 | GRCh38.p7 | 17:60214648 | AGCCACAGGCGCATA[C/T]CTTCCTCTTTAATGC | 84669 |
rs754398288 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60340431 | AAAAATACAAAAATT[A/C]TTTGTCTCTTTTGAT | 84669 |
rs754399504 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60197179 | TTAAGAATCTGTCTC[-/A]AAAAAAAAAAAAGAT | 84669 |
rs754412944 | snp | A/G | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423044 | CAGAGTGGTCTGGAC[A/G]GGATCTTCCTTGTTC | 84669 |
rs754415410 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60288801 | CTGTCTACAAAGGAA[A/G]GATTATCTAATAACA | 84669 |
rs754445695 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306514 | GTTGTGGTGGGCGCC[C/T]ATAATCCCAGCTACT | 84669 |
rs754447433 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60320288 | TCTAAATAAATACCC[C/T]AAAACATTTCTAATA | 84669 |
rs754479699 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60327852 | ACTGTCACAGCCCGG[C/T]CAGGTATGTGGACAC | 84669 |
rs754480396 | snp | G/T | 1.82334e-05 | 0.00301933 | intron-variant | USP32 | GRCh38.p7 | 17:60183499 | TTAAAGGGTTCTGAA[G/T]ATACAAAATTTACAT | 84669 |
rs754482719 | snp | A/G | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422687 | AGGAGGGTCCCGGAG[A/G]GGCTGGTTTTGGAAA | 84669 |
rs754500694 | snp | C/T | 0.000100385 | 0.00708395 | intron-variant | USP32 | GRCh38.p7 | 17:60271521 | ATAAAACCTCAGAAT[C/T]CTCTTCTCAGGAGTT | 84669 |
rs754514584 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60269603 | CAGCCAAGCTTCCTA[A/G]TGTTAATAATGACAT | 84669 |
rs754524139 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406664 | GTGATTACAGGCACG[C/T]GCCACCACGCCCAGC | 84669 |
rs754525774 | snp | G/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419358 | ACACACACTGGGGCC[G/T]ACCAGAGAGTGGAGG | 84669 |
rs754532413 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256121 | AGGCAAGAGGATCGC[C/T]TGAGCCCAGGAGCAT | 84669 |
rs754539361 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60383382 | GAAAGCTCTCCACAA[C/T]TTCTCTCCATTATTT | 84669 |
rs754554007 | snp | A/C | 0.000131036 | 0.00809325 | missense | USP32 | GRCh38.p7 | 17:60213603 | TACCAGGTGTTGTTC[A/C]TCCTGGATTTTCAAA | 84669 |
rs754565783 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60330134 | GAATCCTCCTCAGGT[C/T]CGCTGGTGCCCAAAA | 84669 |
rs754570695 | snp | A/G | 1.65146e-05 | 0.0028735 | synonymous-codon | USP32 | GRCh38.p7 | 17:60185591 | GGAGACAGCTGTCCA[A/G]GTTGATGGGCTCGGC | 84669 |
rs754622278 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60272859 | TATGCCAAGAAAGGG[A/C]TCCAGAAATCTGCAC | 84669 |
rs754622831 | in-del | -/A | 0.00260926 | 0.0360253 | intron-variant | USP32 | GRCh38.p7 | 17:60223591 | ATACAGAAAGCCTAT[-/A]AAAAAAAAAGAGGAT | 84669 |
rs754658667 | snp | C/T | 1.6552e-05 | 0.00287676 | intron-variant | USP32 | GRCh38.p7 | 17:60180500 | GTTCCCCAGTTCTGT[C/T]GATATTCTGTTTCTA | 84669 |
rs754659910 | snp | C/G/T | 3.29458e-05 | 0.00405857 | synonymous-codon | USP32 | GRCh38.p7 | 17:60226100 | TGAAAATTTCTCTTC[C/G/T]GTAGTATTCACGTAA | 84669 |
rs754663903 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60345328 | TAAGAACACAGCCAC[A/G]TTGACATCTAAAACA | 84669 |
rs754716596 | snp | C/T | 1.64819e-05 | 0.00287066 | missense | USP32 | GRCh38.p7 | 17:60181536 | GCACATGCCCTCGAC[C/T]CAAGGCGTCAGCCAG | 84669 |
rs754735502 | snp | C/T | 8.23554e-05 | 0.00641646 | intron-variant | USP32 | GRCh38.p7 | 17:60210988 | TTAGGAATTAAATAC[C/T]TTTATATTATTTTAA | 84669 |
rs754743853 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60389367 | GCTAACATGATGAAA[-/C]CCCATCTCTACTAAA | 84669 |
rs754758992 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60224735 | TTACAGTGAGCTATG[A/G]TCATGCCATTGCACT | 84669 |
rs754766267 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60398831 | AAAAAAAAAAATTTA[A/G]TTAGCTGGGTGTAGT | 84669 |
rs754769171 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60274420 | TTCATGAAAACTATA[C/T]TCCCACAGATCCAGA | 84669 |
rs754776019 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60329198 | GTGTTAAATAATACT[G/T]CCAGAAAAAAACAAA | 84669 |
rs754779692 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60401743 | AAAAAAAAAAAAGAA[A/G]GAAAGTAGATCTCTG | 84669 |
rs754791389 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392665 | AGGGAGCTCCCAACC[G/T]TAGGGACGTCTTTGA | 84669 |
rs754829647 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295988 | TGTTTAAGGACACAT[-/A]AACATGTTGTATAAA | 84669 |
rs754831296 | in-del | -/CCC | | | intron-variant | USP32 | GRCh38.p7 | 17:60197361 | GTAATCCCAGCACTT[-/CCC]TGGGAGGCTGAGGCA | 84669 |
rs754831986 | snp | C/G | 1.67798e-05 | 0.00289648 | synonymous-codon | USP32 | GRCh38.p7 | 17:60252422 | AGTAGCTGGTCTTAA[C/G]CCCAGAACTATGTGA | 84669 |
rs754850841 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60374772 | AAAAAGCAAAAACAA[C/G]TAAATGGCTACGATG | 84669 |
rs754869304 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227804 | CAGTTATAAATTTCT[G/T]TGTTCCTTGTCTGTT | 84669 |
rs754877373 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60307940 | GTTGAAGAGCACACT[C/G]ACAGGCACTGGCAGA | 84669 |
rs754884941 | snp | A/G | 1.72859e-05 | 0.00293984 | missense | USP32 | GRCh38.p7 | 17:60181667 | CCTTTGCTCCTCCCC[A/G]AAGTCCGTGGGCTGC | 84669 |
rs754890537 | in-del | -/C | 0.000115703 | 0.00760515 | intron-variant | USP32 | GRCh38.p7 | 17:60255289 | TCATGTTAGGAACAT[-/C]TTTTTTTTCTTTTTT | 84669 |
rs754899446 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60274820 | AAGGCTAACAATGTT[-/A]ACTTCTCTGCCTCAA | 84669 |
rs754913800 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60314489 | CTGAATAAAAGAGCA[A/G]TGAACTTGAAGAAAC | 84669 |
rs754928694 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415719 | CACTCCAGCTATGAC[A/C]GGGATTTCAATGGCC | 84669 |
rs754948064 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60373606 | AGGCGTGCACCACCA[A/C]AACCGGCTAATTTTT | 84669 |
rs754949506 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60281302 | CCAGCACTTCGGGAG[A/G]CCGAGGCGGATGGAT | 84669 |
rs754964725 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60324583 | TCACCTTTGATACTT[G/T]ATCTTTTCTTTGTTT | 84669 |
rs754966558 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290402 | GTTGCAGGGACATAT[A/G]AGTACACTGCCAACA | 84669 |
rs754967290 | snp | A/C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60263165 | GTTACCCAGGCTGGT[A/C/T]GAGAGCTCCTGGGCT | 84669 |
rs754972613 | snp | C/T | 7.76247e-05 | 0.00622947 | intron-variant | USP32 | GRCh38.p7 | 17:60288705 | TAAAACAAGAAAACA[C/T]AAGTTTAGTCAAATT | 84669 |
rs754975187 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407032 | TTGGACAATTGGCAG[C/T]GCAGAACTGACGTCA | 84669 |
rs754987271 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403261 | GACCTCGTGATCTGC[C/T]GGCCTCGGCCTCCCA | 84669 |
rs754990595 | snp | C/T | 3.21404e-05 | 0.00400864 | intron-variant | USP32 | GRCh38.p7 | 17:60219600 | TTTTAAGGAAATGCA[C/T]GGTATTCTTGCTGCA | 84669 |
rs754994597 | snp | A/G | 4.98144e-05 | 0.00499047 | intron-variant | USP32 | GRCh38.p7 | 17:60205673 | TCTACAAATTCAAAG[A/G]TAAGTACAGTATCAT | 84669 |
rs755008497 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393637 | AGTTCCTAAAACCAA[C/T]AGATTCTAATATACC | 84669 |
rs755014007 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60243606 | TTTATATAATTGTAA[G/T]GTGTCACAAAATATT | 84669 |
rs755058035 | snp | A/G | 7.83812e-05 | 0.00625975 | synonymous-codon | USP32 | GRCh38.p7 | 17:60208666 | TACCTGTTATTTCTA[A/G]GTGCATATAACTGTC | 84669 |
rs755079038 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60304818 | AGCCTAACATTGACC[A/T]CATTAATAAACTCTT | 84669 |
rs755102329 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60236437 | CATAGGGCAGTATCA[A/G]GAATAATTACTTCAG | 84669 |
rs755110144 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60284373 | GGTCTGCCACCATGG[C/T]TGGCTAATTTTTGTA | 84669 |
rs755127018 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60289634 | GCTGAAAAAGAGCAT[C/T]ATATGGTTGTTCACG | 84669 |
rs755132565 | snp | A/G | 1.65422e-05 | 0.0028759 | intron-variant | USP32 | GRCh38.p7 | 17:60271334 | GAACATATGTAGAAA[A/G]TGGAATGATCCCTAC | 84669 |
rs755148049 | snp | A/G | 1.75207e-05 | 0.00295973 | intron-variant | USP32 | GRCh38.p7 | 17:60208875 | AAAATCCAAAAGAGA[A/G]GCATTTCTATATAAA | 84669 |
rs755182464 | snp | A/T | 1.67722e-05 | 0.00289583 | intron-variant | USP32 | GRCh38.p7 | 17:60192815 | AAGCTGAAATTCTAC[A/T]AAAGTAATTCTTTTG | 84669 |
rs755184628 | in-del | -/TT | | | intron-variant | USP32 | GRCh38.p7 | 17:60189065 | TATAGAGCCAAATAA[-/TT]TGTCATCATTGACAG | 84669 |
rs755192115 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60369945 | AGGTCTCACTATGTT[A/G]CCTAGGCTAGTCTCG | 84669 |
rs755197740 | snp | A/G | 1.67363e-05 | 0.00289272 | intron-variant | USP32 | GRCh38.p7 | 17:60192957 | GAGAACAAAAAGAGT[A/G]TAAGAAGCATTTCTG | 84669 |
rs755212204 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60320533 | ATCAAACGTGCACAC[C/T]GTTGGGATGAGGGAA | 84669 |
rs755228289 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60350806 | TAATGTACCCTACTC[A/G]GGTGATGGGTGCATT | 84669 |
rs755232012 | in-del | -/AT | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412087 | GCCAGCTCTAGCACA[-/AT]ATCAGAGAATCTGTA | 84669 |
rs755256443 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60180933 | TATCACCCAGGCTGG[A/G]GTGCAGTCGAGTGAT | 84669 |
rs755262528 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295240 | AAGAGCAAAACTTCG[-/A]AAAAAAAAAAAAGAT | 84669 |
rs755300389 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60237558 | GATACACCTCAATTA[A/G]AAAGTCATCCATTAA | 84669 |
rs755304772 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60282607 | TCCACCCATCTCGGC[C/T]TCCCAAAGTGCTGGG | 84669 |
rs755305643 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60260910 | ACAAAACAAAAAAAA[C/T]CCAGAAGAACTGCAA | 84669 |
rs755316916 | snp | C/T | 0.000102349 | 0.0071529 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422550 | AGAAGCCAGAGGGGA[C/T]GTGGGGAGTGCCACC | 84669 |
rs755317579 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411608 | TCAAACTAATGGGCT[C/T]AAGTGATCCTCCCAC | 84669 |
rs755318172 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon | USP32 | GRCh38.p7 | 17:60345592 | ATCCTTCAGTCGTTT[C/T]AGCTCTACATCTGTA | 84669 |
rs755318661 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388105 | ATCTGCTGAATTAAT[G/T]AGCAAAAGGACATTT | 84669 |
rs755325080 | snp | A/G | 3.31895e-05 | 0.00407353 | intron-variant | USP32 | GRCh38.p7 | 17:60225995 | AGAAAGACCTATCCA[A/G]GGGGAATAAACCAAT | 84669 |
rs755371709 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60231004 | ATTATCCTAGAACCC[C/T]GGTTTTCAGAAGATA | 84669 |
rs755373374 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60382007 | TGCATGGTGAACTCA[C/T]TTTTAAGACCAAATT | 84669 |
rs755378454 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264718 | ACAAAAAAATCAGCC[A/G]GCATGGTGGCACACA | 84669 |
rs755389048 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60355006 | CCGAGATAGCGCCAC[C/T]GCACCCCAGCCTGGG | 84669 |
rs755394255 | in-del | -/TCTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60248556 | TTGGTCTTCTTTCTC[-/TCTT]TCTGATGAAATAATC | 84669 |
rs755394434 | in-del | -/ACAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60283128 | AATTGGGCTTTGATG[-/ACAA]ACAATCATCTCAATT | 84669 |
rs755396303 | snp | C/T | 1.67265e-05 | 0.00289188 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205462 | CATTTTTCGGTGGAC[C/T]GCAATGATGTAACCT | 84669 |
rs755397565 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60259373 | ATTCACGTAACAATG[C/T]TGTGATGTAAAAAAA | 84669 |
rs755409880 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60398400 | ACCTTGCCTCAAAAA[A/G]AGAAAAAAGAAAAAA | 84669 |
rs755429623 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60311757 | TTAAACCCAGGAGGC[A/G]CACGTTGCAGTGAGC | 84669 |
rs755440798 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60335521 | TATAAACTAAAACAC[A/C]AGTTGTACCTCTTCT | 84669 |
rs755463663 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60245499 | GTTTGTTTTTTGTTG[A/C]TGAACCTTCTACAAA | 84669 |
rs755470394 | snp | A/C | 0.000214223 | 0.0103472 | missense | USP32 | GRCh38.p7 | 17:60219679 | TCATACCCATATTCA[A/C]CCAGATGTTAGACTG | 84669 |
rs755481725 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60190492 | GTCTAAAACAGAAAT[A/G]GCATAATAGTTACAC | 84669 |
rs755492272 | snp | C/T | 4.9579e-05 | 0.00497866 | synonymous-codon | USP32 | GRCh38.p7 | 17:60301651 | GACAAGTCCAACTAT[C/T]AAATTATTGAAGTGC | 84669 |
rs755492379 | snp | C/T | 3.29489e-05 | 0.00405874 | missense | USP32 | GRCh38.p7 | 17:60205572 | CAACAGTGTTTGGCA[C/T]TCCATTGGGGATGAA | 84669 |
rs755492407 | snp | A/G | 3.29516e-05 | 0.00405891 | missense | USP32 | GRCh38.p7 | 17:60183239 | TCCTCTTCCCCAGCC[A/G]AACTCTGCGCATCCA | 84669 |
rs755505984 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378737 | AGAATAGGCAAATTC[A/G]TAAAAACAGAAAGTA | 84669 |
rs755534102 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412961 | CACGCTCTAAAGTTC[C/T]GAGGTTGCCATTCTG | 84669 |
rs755552276 | snp | A/T | 3.37975e-05 | 0.00411067 | intron-variant | USP32 | GRCh38.p7 | 17:60252451 | GACACACCTAGGGAA[A/T]AAAATGGTAAATCAA | 84669 |
rs755552495 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60309149 | AATGGGATTTGATCA[A/T]GCTAAAAACTTCTGC | 84669 |
rs755580051 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60363225 | TTTGGGAGGCTGAGG[C/T]GGGCAGATTGCCTGA | 84669 |
rs755581193 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60293133 | GATTCAGATTTTCTC[G/T]ATTACCACCTTCTTC | 84669 |
rs755607627 | in-del | -/ATAC | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295816 | TAATCTTTATCATAG[-/ATAC]ATATGTATAGGAAGA | 84669 |
rs755638485 | snp | C/T | 6.4043e-05 | 0.00565839 | intron-variant | USP32 | GRCh38.p7 | 17:60252336 | GTAACCAATATATTT[C/T]AAGTATGTGAAATTT | 84669 |
rs755642562 | snp | C/T | 3.30923e-05 | 0.00406756 | synonymous-codon, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294755 | TCTTTCCATTTCTTC[C/T]CGTATAACATAGTTC | 84669 |
rs755665587 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242160 | TTGTACAGGCTGGTA[G/T]GAGGTGGCTATTCAC | 84669 |
rs755686290 | snp | C/T | 3.37137e-05 | 0.00410557 | intron-variant | USP32 | GRCh38.p7 | 17:60211340 | GGTTTATATCAAAGT[C/T]ACAGGTTAAGAGGCC | 84669 |
rs755698725 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60269151 | AAAATATTTCCTAAA[C/T]GTTTAAAATTTTCAA | 84669 |
rs755705557 | snp | A/G | 1.65348e-05 | 0.00287526 | intron-variant | USP32 | GRCh38.p7 | 17:60180679 | TGTTAGCAGTTAACT[A/G]TACTATGGCCAGGGT | 84669 |
rs755711542 | in-del | -/AACAGGC | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416380 | GCATGATGATTATGA[-/AACAGGC]GTATGCCATCAAAGA | 84669 |
rs755732154 | snp | C/G | 1.65154e-05 | 0.00287358 | intron-variant | USP32 | GRCh38.p7 | 17:60288730 | CAAATTTTAAGGTAT[C/G]TTACTTGGAACCTGC | 84669 |
rs755773658 | in-del | -/TTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60191504 | GTTCCAATGCCTACT[-/TTA]TTATTATTATTATTA | 84669 |
rs755776063 | snp | A/C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60367116 | ACAGGCGTGAGCCAC[A/C/T]GCGCCTAGCCTAAGC | 84669 |
rs755779053 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60294456 | TGTTTCATTATACTC[G/T]AAGTATGAATAGTTG | 84669 |
rs755825780 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60329266 | TGTTTTTGCCTGACA[A/G]TGTGTGTGTGTGTTT | 84669 |
rs755844493 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264978 | ATTAATCTGCACACC[C/G]CTGAAATCACTATTC | 84669 |
rs755844653 | in-del | -/AC | | | frameshift-variant | USP32 | GRCh38.p7 | 17:60208699 | TTGGTAGTGGCAAAG[-/AC]AAAAAATTGAAAGGG | 84669 |
rs755858647 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60273296 | TGCTAGGAAACTGTA[A/C]GCTAAAAAAGTCCTA | 84669 |
rs755881700 | snp | A/T | 1.64961e-05 | 0.00287189 | intron-variant | USP32 | GRCh38.p7 | 17:60198467 | TACAAACAAGAGAAT[A/T]GAGAGTTCAGAAGAC | 84669 |
rs755882459 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60375451 | TGAGTACTTAAAGGA[A/C]CGTCTACAATGCACC | 84669 |
rs755885514 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407711 | TGCTTGAACCCAGGA[A/G]GCGGAGGTTACAGTG | 84669 |
rs755886156 | snp | C/T | 1.80393e-05 | 0.00300322 | intron-variant | USP32 | GRCh38.p7 | 17:60183118 | AGAAACATATGTAGC[C/T]TACAGGAGTCCCAAG | 84669 |
rs755888630 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306830 | TGATAAATTGAGGAA[A/G]GATTGCAGGATAGAA | 84669 |
rs755922977 | in-del | -/ATA | | | intron-variant | USP32 | GRCh38.p7 | 17:60380844 | GTGGGCACCCAAATT[-/ATA]ATAAGAATTAGAAAT | 84669 |
rs755932321 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60315461 | AGAATGTAAAAAAAC[C/T]CCTGCAACATCTATA | 84669 |
rs755956052 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60394766 | TTTATTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 84669 |
rs755974360 | snp | A/T | 1.64855e-05 | 0.00287097 | missense | USP32 | GRCh38.p7 | 17:60223492 | CAACAAAATATTCCC[A/T]TTGGCTCCCAGCAAA | 84669 |
rs755983597 | snp | C/T | 1.71032e-05 | 0.00292426 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391974 | CGGGGGGTCGGAGCC[C/T]GATCTCGCCCCCACC | 84669 |
rs755983764 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60330933 | TTTCCAAGTCAATGG[C/T]AGAACATCACAAGTT | 84669 |
rs755987436 | snp | C/G | 3.45375e-05 | 0.00415543 | intron-variant | USP32 | GRCh38.p7 | 17:60223367 | TGAAATTTATTAATA[C/G]CTTGCAAGAGAATAA | 84669 |
rs756008798 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60194795 | CTTTTTGGGTTACTT[A/G]CTTATTCGAACATCC | 84669 |
rs756029355 | snp | C/T | 1.64991e-05 | 0.00287215 | missense | USP32 | GRCh38.p7 | 17:60255254 | TCCAGAGTAAGATGA[C/T]CCATCTGAAACAGAG | 84669 |
rs756035231 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360360 | AATACAAAAAATTTT[C/T]GTATTTGTATTTTGT | 84669 |
rs756035565 | snp | C/T | 3.53107e-05 | 0.00420168 | missense | USP32 | GRCh38.p7 | 17:60207104 | CCACTCACTGAGAGT[C/T]GTACTTTTTGGTTGT | 84669 |
rs756045258 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378790 | GGGAAAAAAAGGGAT[A/G]GAGAATTTCTGTTTG | 84669 |
rs756056159 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60303195 | TAAACAGAACTAATA[C/T]ACTTTGTAAAATAAC | 84669 |
rs756087533 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60358505 | ATTGAACCCAGTAGG[C/T]AGAGGCTGCAGTGAG | 84669 |
rs756087858 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417279 | TCTTGATCCATATTT[A/G]TGTCCACTTATGAAG | 84669 |
rs756096347 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194001 | TTTGCTCTAACTGAA[C/T]GAAGCCTGGCTTTCT | 84669 |
rs756098965 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60316517 | GTATTTTTAATATTG[C/T]CTCTCTTCTGTGTTG | 84669 |
rs756123947 | snp | A/G | 0.000297167 | 0.0121859 | synonymous-codon | USP32 | GRCh38.p7 | 17:60185604 | CAGGTTGATGGGCTC[A/G]GCTTGCGCTCGCCGA | 84669 |
rs756128700 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60277693 | TTATAAAGTCCCATC[A/C]CCAAAATTAGAATTT | 84669 |
rs756135535 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60276947 | GTAGATTACATATAC[-/AT]ATATATATATATATA | 84669 |
rs756141801 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60327357 | GGCAGTGGGTCCCCT[A/G]TGCTCCACGTCACCG | 84669 |
rs756145276 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60239595 | TGCTCATATCTGATG[A/G]AGAACCCCTCTAATA | 84669 |
rs756146792 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60204155 | ACTTGATTTTCCTCA[A/C]GAACATTCTTGTATC | 84669 |
rs756154123 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60249152 | GAGGTTGTGCTCTCA[G/T]CAGTTTACTGGTTGT | 84669 |
rs756161438 | snp | G/T | 3.29549e-05 | 0.00405911 | missense | USP32 | GRCh38.p7 | 17:60345482 | AACAAAAAGATTACC[G/T]CAGCAACCTTTGGAG | 84669 |
rs756166667 | snp | C/T | 1.79564e-05 | 0.00299631 | missense | USP32 | GRCh38.p7 | 17:60208114 | TCTGAATTAAGTCCA[C/T]AGAGATCACTCAGCT | 84669 |
rs756181962 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, utr-variant-5-prime, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266071 | CTCCATCACGGTCAA[C/T]ATCAAATACCTTGAA | 84669 |
rs756183785 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | USP32 | GRCh38.p7 | 17:60219696 | CAGATGTTAGACTGC[C/T]GTGTCCGAGTGGCAG | 84669 |
rs756197533 | in-del | -/GCC | 1.76298e-05 | 0.00296894 | intron-variant | USP32 | GRCh38.p7 | 17:60183149 | AAGCACCTGCATAAG[-/GCC]GCCCCCAGGCCTCAC | 84669 |
rs756207619 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60313677 | ATCCAGAGCATTGAG[A/G]AGAGACCCCAAGAGT | 84669 |
rs756210335 | in-del | -/AC | | | intron-variant | USP32 | GRCh38.p7 | 17:60186707 | TAAGTATAAGAAAGG[-/AC]AGAGAGCAAAGAATG | 84669 |
rs756270591 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60246026 | TCATTTTTTTGGGTT[A/G]GGAATATTCCGAATC | 84669 |
rs756280393 | snp | A/C | 1.64887e-05 | 0.00287125 | missense | USP32 | GRCh38.p7 | 17:60181552 | CAAGGCGTCAGCCAG[A/C]TCACATATCTGCCCA | 84669 |
rs756318506 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413263 | ATAGAACTGGGGTCC[A/G]CTCACCTGGCCCAGC | 84669 |
rs756344947 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60314568 | AACTGGGGGTGGGGG[-/G]AGGAAAGGAGAGAAA | 84669 |
rs756385302 | snp | C/T | 1.64741e-05 | 0.00286998 | stop-gained | USP32 | GRCh38.p7 | 17:60236156 | TTTGACATATTCTTT[C/T]CACTGTTGCCACCAC | 84669 |
rs756405559 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60350115 | CCTCCCAGGCTCAAG[A/C]AATCCTCCCACCTCA | 84669 |
rs756410685 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415228 | TGGATGTAGGCTGCT[A/G]GCAGGGAAGACACAG | 84669 |
rs756436165 | in-del | -/TCTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60237117 | AAAAAATCTACTCTA[-/TCTA]TCTATCTATCTATCT | 84669 |
rs756440624 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60371999 | CTCATAAGGTAAACA[C/T]TTAACAGTTATCTAA | 84669 |
rs756459754 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, utr-variant-5-prime, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266056 | CAACCCTGGAGAGAA[C/G]TCCATCACGGTCAAC | 84669 |
rs756472820 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256263 | AAAACAAAAACTCAT[C/T]TTTGTTTTTTCAAAA | 84669 |
rs756473235 | snp | C/T | 3.31296e-05 | 0.00406985 | synonymous-codon, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271477 | AATGATGTCTGATTC[C/T]TCCACTAAGGGTCAA | 84669 |
rs756492301 | snp | A/G | 6.58979e-05 | 0.00573974 | missense | USP32 | GRCh38.p7 | 17:60183335 | TTATGCTGGCAGAGA[A/G]CCGGGTCTCTTGGTA | 84669 |
rs756513011 | snp | A/C | 1.64953e-05 | 0.00287182 | missense | USP32 | GRCh38.p7 | 17:60198278 | TCCTGGGCATGATTA[A/C]TAGCTTCCTGAGGTG | 84669 |
rs756517269 | snp | C/T | 3.40634e-05 | 0.00412681 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183430 | CCGACCATTTACAAA[C/T]TGAAATCGCTTAAGG | 84669 |
rs756532610 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60362337 | ATCAACCAGTAACAA[-/T]TTATAAACTTTAGAG | 84669 |
rs756543451 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60300138 | GACCCAGCATATGGT[C/G]TTCAAGAATAAAAGC | 84669 |
rs756545622 | in-del | -/CGTCAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60327364 | GTCCCCTGTGCTCCA[-/CGTCAC]CGTCACCGAAGCAGC | 84669 |
rs756546968 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60356402 | CCATATCTCTCACTT[C/T]GGCTGACCTTAAACC | 84669 |
rs756552577 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60385209 | ACCTCGTGACCCCCG[C/T]CCCTGCCTGCAAGAG | 84669 |
rs756575459 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | USP32 | GRCh38.p7 | 17:60226112 | TTCTGTAGTATTCAC[A/G]TAACTGAGGCTGCTT | 84669 |
rs756586487 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60287593 | AAGCAGACCCAATTG[C/T]GATTCTATAACAGGA | 84669 |
rs756620774 | snp | C/T | 1.65468e-05 | 0.00287631 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265944 | CCCATTGGAAGTTTA[C/T]ACGCAACAAGACATA | 84669 |
rs756635482 | snp | A/G | 2.29445e-05 | 0.00338699 | intron-variant | USP32 | GRCh38.p7 | 17:60209328 | ATTTGTGGCCAGAAC[A/G]TTTTGTCTATTGCTT | 84669 |
rs756636706 | snp | A/C | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423857 | ATAGTCATTAGATGC[A/C]TGGTTTATTAGTCCA | 84669 |
rs756639752 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60400588 | AGAAGCAGAGCTTTG[A/G]ACATATTACATTTGA | 84669 |
rs756661169 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191277 | CATGGTGGCAGGCAC[C/T]TATAATCCCAGCTAC | 84669 |
rs756670921 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60294113 | GTCTTGCTACATTGT[C/T]CAGGCTGGTCTTGAA | 84669 |
rs756704938 | snp | C/T | 0.000131778 | 0.00811614 | missense | USP32 | GRCh38.p7 | 17:60181421 | CCAAGCTGACCATTG[C/T]TGTAGCCATTGCCAC | 84669 |
rs756711104 | snp | C/T | 1.65023e-05 | 0.00287244 | intron-variant | USP32 | GRCh38.p7 | 17:60345617 | TCTGTAACTGCAATT[C/T]AGAAACAGAAGATGG | 84669 |
rs756716309 | snp | A/G | 1.67158e-05 | 0.00289096 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179244 | GCTGTCTAGCAGCCA[A/G]AGTGGTAGCTTTACT | 84669 |
rs756725817 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60358159 | ACTTTTTTATTGCAA[-/AT]ATAGAGTATTTCAGC | 84669 |
rs756738383 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60331061 | CTTAAGTGACTAGGA[A/G]AAGATCATTAAGTAA | 84669 |
rs756746789 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296711 | TAAAAAATTGTTACC[A/T]GTTGTACCTCAGTAT | 84669 |
rs756750212 | in-del | -/CAT | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378555 | AACTCAAATATGTCC[-/CAT]CAACAGATGGATGTA | 84669 |
rs756761907 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60294587 | CAAGAGTAATCTGCA[C/T]ATAAACATCTGTTTG | 84669 |
rs756762218 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60350224 | TTTGCCATGTTGCCC[A/G]GACTGGTCTCAAACT | 84669 |
rs756771084 | snp | A/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409590 | TGCAAAAATTACAAG[A/T]GAGATAAATCTGACA | 84669 |
rs756796530 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60229749 | TTGGCAAGGTAATCC[A/G]TTTATAAATTTATAC | 84669 |
rs756798275 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60242452 | GAGTCTCACCGTCAC[C/G]CAGGCTGGGGTGTAG | 84669 |
rs756805998 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60187465 | AACTGATGTGCTTCA[A/G]AAGGAAACGTGCTGC | 84669 |
rs756806668 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378333 | ATGGAAGGAGCACTT[A/G]TGCATTGCTGGTGGA | 84669 |
rs756811011 | in-del | -/CAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60210911 | TGAAGGATCCAAAAA[-/CAT]CATTTATTAAGTTAA | 84669 |
rs756815311 | snp | A/T | 1.66432e-05 | 0.00288467 | missense | USP32 | GRCh38.p7 | 17:60205479 | CAATGATGTAACCTG[A/T]AAAGGGGCTGTCAGG | 84669 |
rs756818090 | snp | C/T | 1.65225e-05 | 0.00287419 | intron-variant | USP32 | GRCh38.p7 | 17:60255274 | CTGAAACAGAGACAC[C/T]CATGTTAGGAACATC | 84669 |
rs756830486 | in-del | -/AGAT | 1.70945e-05 | 0.00292351 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294815 | GTCTAAGAAAAAGAA[-/AGAT]AGAATAAATTAATCT | 84669 |
rs756838028 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60203902 | TATAAAATTAAGACA[C/T]TAAAGTCCAAAGAGC | 84669 |
rs756842736 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60360013 | GCTGGGACTACAGGC[A/G]CCCACCACCACACCT | 84669 |
rs756860752 | snp | C/T | 1.66192e-05 | 0.00288259 | missense | USP32 | GRCh38.p7 | 17:60212036 | TACCCTTGTGTCTAT[C/T]TATTTTACTACTATT | 84669 |
rs756871406 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194089 | ACTCTGTTGCCCAGG[C/T]TGGAGTGCAGTGGCG | 84669 |
rs756901938 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60315641 | AATATTCACAGCAGC[A/G]TTATTGACAATAGAA | 84669 |
rs756903827 | snp | C/T | 1.66601e-05 | 0.00288614 | missense | USP32 | GRCh38.p7 | 17:60301617 | TTGCTTTCTCTTCAT[C/T]TTTGCCTCTTGTAAG | 84669 |
rs756913645 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60283280 | TAGTTGAGGCAAAGA[A/G]CACACGTGAGGAGAA | 84669 |
rs756914873 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60396696 | GAGTTTAAGACACAC[A/G]GGATTCCTAAATTAA | 84669 |
rs756919354 | snp | C/T | 1.65666e-05 | 0.00287802 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294765 | TCTTCCCGTATAACA[C/T]AGTTCCCAGATTCAC | 84669 |
rs756944218 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60365279 | GGTTAGGAGTTAGAG[-/A]ACCAGCCTGGCCAAC | 84669 |
rs756975256 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60374160 | CTGCACTCTAGCCTC[A/T]GGGACAGAGTGAGAC | 84669 |
rs756983439 | snp | A/G | 3.29468e-05 | 0.00405861 | missense | USP32 | GRCh38.p7 | 17:60205581 | TTGGCATTCCATTGG[A/G]GATGAATATTGGTCG | 84669 |
rs756990616 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195082 | CATAACTTTACCAAG[C/T]ACCACTAGAATCAGG | 84669 |
rs757013642 | snp | C/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420283 | ATAGGTGTGAGCCAC[C/T]GCACCCGGCAGAATT | 84669 |
rs757030992 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265665 | GGCTTCCCAAAGTGC[A/G]GAGATTCCAGGCAAG | 84669 |
rs757039527 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395110 | TACAGTTTAAAAAGC[A/G]GTGTAATCTTACATG | 84669 |
rs757054766 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60316685 | GTCTCTACTAAAAAT[A/T]CAAAAATGAGTCGGG | 84669 |
rs757067114 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60199141 | GAAATGAAAAGATGC[C/T]AGTGGAAAAAAAAAA | 84669 |
rs757107971 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60284151 | ATTAGAAGGTCATTA[C/T]TGTAGGTGAAACAAT | 84669 |
rs757111280 | snp | A/G | 0.0012164 | 0.0246317 | synonymous-codon, intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422613 | GGCCTCAGATGGGCA[A/G]GGGGGTGAAGGGGAC | 84669 |
rs757120597 | snp | C/T | 5.37418e-05 | 0.00518344 | missense | USP32 | GRCh38.p7 | 17:60208145 | GTTTTTTTAAACCTG[C/T]GTACTTTTCATCCAT | 84669 |
rs757128107 | in-del | -/TCG | 1.65149e-05 | 0.00287353 | cds-indel | USP32 | GRCh38.p7 | 17:60185602 | TCCAGGTTGATGGGC[-/TCG]GCTTGCGCTCGCCGA | 84669 |
rs757133011 | snp | A/T | 1.65192e-05 | 0.00287391 | intron-variant | USP32 | GRCh38.p7 | 17:60271343 | TAGAAAATGGAATGA[A/T]CCCTACCTTCACTTA | 84669 |
rs757151472 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60380704 | CATGGGAGAAAAAAA[C/G]CTCCTAAAATTGCAT | 84669 |
rs757162287 | in-del | -/TTTAT | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420074 | ATTTATTTTGTTTAT[-/TTTAT]TTTATTTTATTTTAT | 84669 |
rs757169185 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405449 | AGCTCAGACAGTCCA[C/T]CCGCCTCAACCTCCC | 84669 |
rs757175165 | snp | C/T | 1.86949e-05 | 0.0030573 | intron-variant | USP32 | GRCh38.p7 | 17:60223616 | GAGGATAGAATCTCT[C/T]ATTTTTAGTTATTAT | 84669 |
rs757176839 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60324285 | GACCGTGTTTCAAAT[-/AT]ATATATATATATATA | 84669 |
rs757194918 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60282331 | GTGTAAGTATCATAA[C/T]TCATTTCCCCCTAAA | 84669 |
rs757228324 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60177493 | TTAAAAAAATTAATT[A/G]CAACCAGTATAACAA | 84669 |
rs757242855 | snp | A/C | | | upstream-variant-2KB, intron-variant, stop-gained | C17orf64, USP32 | GRCh38.p7 | 17:60422339 | GCCAAAGTCTTCGCT[A/C]GACCCCGCACATCTT | 84669 |
rs757256225 | snp | C/T | 1.76446e-05 | 0.00297018 | intron-variant | USP32 | GRCh38.p7 | 17:60181284 | GACAAGTGAACAAAA[C/T]ACAGACCACTCTCTG | 84669 |
rs757258570 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60263062 | CAAATGATCCTCTCG[C/T]CTCAGCCTCCCTTGT | 84669 |
rs757268598 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60225636 | TTCACTACAGCCTCT[A/G]TCAAATTAGACTGCC | 84669 |
rs757276111 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290594 | TTTCTTAGTGGTTGC[A/G]ATATTGTTAAATATA | 84669 |
rs757276503 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403311 | ATGAGCCACTGCGCC[C/T]AGCCAAGCTGTATCT | 84669 |
rs757286500 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242800 | CCTTAGGTAAATTGT[G/T]AAATCAGGAAGTCTA | 84669 |
rs757291663 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60314013 | ACAGCTATTATAAAT[A/C]TGCTCAAGAATTTAA | 84669 |
rs757291832 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60300376 | ATATCCCACGAAACA[C/G]ACGGACACTAAGCAA | 84669 |
rs757298442 | snp | A/G | 3.30011e-05 | 0.00406195 | intron-variant | USP32 | GRCh38.p7 | 17:60190692 | GCAAAATCTAAAAAG[A/G]GGGAAAAGATCCACA | 84669 |
rs757320673 | snp | C/T | 3.4805e-05 | 0.00417149 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391989 | TGATCTCGCCCCCAC[C/T]CCCCTCCCGCCTTCT | 84669 |
rs757322107 | snp | A/G | 1.73384e-05 | 0.0029443 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181681 | CAAAGTCCGTGGGCT[A/G]CTATTAGGGCTGCTG | 84669 |
rs757344444 | snp | A/C/G | 5.04336e-05 | 0.00502142 | intron-variant | USP32 | GRCh38.p7 | 17:60391876 | CCCAGACCCCTCCCC[A/C/G]CTCACCTCTCCTCAG | 84669 |
rs757347774 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60190776 | CCTTCCTACTTTTCT[C/G]CTTTCCTCTTGGGCC | 84669 |
rs757356013 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | USP32 | GRCh38.p7 | 17:60198414 | TGGGGCGATTCTTCT[C/G]AGATGACAGGAAATA | 84669 |
rs757370384 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60349578 | ACTCTGTCTCAAAAG[-/AA]AAAAAAAAAAAAAAA | 84669 |
rs757381391 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312873 | ACAACATAAGGCCCA[C/T]GGTATATGAATACAT | 84669 |
rs757391609 | in-del | -/AA | 1.68223e-05 | 0.00290015 | intron-variant | USP32 | GRCh38.p7 | 17:60211348 | TCAAAGTCACAGGTT[-/AA]GAGGCCAGTGACTCC | 84669 |
rs757415819 | snp | C/T | 1.80289e-05 | 0.00300235 | intron-variant | USP32 | GRCh38.p7 | 17:60183121 | AACATATGTAGCCTA[C/T]AGGAGTCCCAAGAAA | 84669 |
rs757416066 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232917 | ACCTTTAACCTTATA[C/T]AGAGTTTCTATCTGC | 84669 |
rs757430486 | snp | G/T | 1.65364e-05 | 0.0028754 | intron-variant | USP32 | GRCh38.p7 | 17:60345644 | ATGGGTAAGAAATCA[G/T]GAGAGAAAAGAGGTG | 84669 |
rs757439966 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60248750 | TCGTTTAGCTCTTTG[A/T]AAACATTTACAATAG | 84669 |
rs757449507 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60399387 | GGGCTGGGCATGGTG[G/T]CTCATACTTGTAATG | 84669 |
rs757450650 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60293818 | GTCATACTGGTGAAA[C/T]GGAATTGTGTCAAAA | 84669 |
rs757468177 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60356866 | AGGTAAACACTTTAA[C/T]GAACTATTTATAAAC | 84669 |
rs757495273 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60358153 | TCTACTACTTTTTTA[C/T]TGCAAATATAGAGTA | 84669 |
rs757506818 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60221527 | TTTTTTTTTTTGAGA[C/T]GGAATCTCGCTCTGT | 84669 |
rs757507083 | snp | C/T | 3.32414e-05 | 0.00407671 | missense | USP32 | GRCh38.p7 | 17:60214733 | AACAGCCTGTATAGG[C/T]TAATACCCGCTTTAA | 84669 |
rs757511110 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60288932 | TTCATCAATTCAGTA[A/G]AGCAGTACACTGCCA | 84669 |
rs757526443 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264466 | GCTGCAGTGAGCCAA[G/T]ATCCCACCACTGCAC | 84669 |
rs757537811 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60383196 | GGTTGCAGTGATCCC[A/G]AGGTCGCACTCCAGC | 84669 |
rs757539740 | snp | G/T | 1.6525e-05 | 0.00287441 | intron-variant | USP32 | GRCh38.p7 | 17:60222375 | CCCCCATCTATGACT[G/T]CTCCTTATATAAGGC | 84669 |
rs757548007 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60338039 | CTAAAATTGTTGGAC[A/G]CAGGCAAGGCGTGGT | 84669 |
rs757550574 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60342137 | ATTCCTTTCTGTTTG[-/T]TCATTTTCCTTCTAA | 84669 |
rs757563793 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60324800 | CTGAGGTCGGGAGTT[C/T]GAGACCAGCCTGACC | 84669 |
rs757582881 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60205336 | AAATTTTAAAAAATT[A/G]AAGAAAAGAAGAGAA | 84669 |
rs757609295 | snp | C/T | 1.99213e-05 | 0.00315599 | missense | USP32 | GRCh38.p7 | 17:60207116 | AGTCGTACTTTTTGG[C/T]TGTCCTGAGGAAAGT | 84669 |
rs757611287 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415463 | TCCAGAATCACTGCC[A/G]AGAAGGTCCACAAGC | 84669 |
rs757622191 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60189105 | TGTCAGATTTTGTGC[C/T]GACAAAGATTTATGA | 84669 |
rs757632645 | snp | C/G | 0.00119259 | 0.02439 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179253 | CAGCCAGAGTGGTAG[C/G]TTTACTGTAACACAC | 84669 |
rs757642348 | snp | C/T | 1.67335e-05 | 0.00289248 | intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179476 | CCATCACTACTATGG[C/T]TCTAAATCCTTGCCA | 84669 |
rs757645913 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411027 | ACAAAAAAAAAAAAG[G/T]TTTTAAAGTTAGCCA | 84669 |
rs757653958 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60322311 | CCACTATGCCTGGCT[A/C]CCTAAATCATATTTA | 84669 |
rs757664749 | snp | A/C | 1.74964e-05 | 0.00295769 | intron-variant | USP32 | GRCh38.p7 | 17:60209584 | CATTATTTCCTACCC[A/C]TAAAATTTGGAATGA | 84669 |
rs757665381 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60385322 | TCTTTTTGGACTCAG[C/T]CCGCCTGCACCCAGG | 84669 |
rs757677738 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60287793 | TCTTTTTATTACATT[G/T]TGAAAAAAACAAAAC | 84669 |
rs757679223 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60309295 | AACTTACTAGCAAAA[A/T]AACAAAACAAAAACA | 84669 |
rs757707417 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60339058 | GGGATTACAGGAGCC[C/T]GCCACCACGCCCAGC | 84669 |
rs757709580 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60274245 | TTGAAGGACAGGCAA[C/T]AGAAACTATCTAAAT | 84669 |
rs757735118 | in-del | -/TGAAATCAGTATTTTTTTGGTGTTCATC | | | intron-variant | USP32 | GRCh38.p7 | 17:60208380 | AGGGATAATATTAAG[-/TGAAATCAGTATTTTTTTGGTGTTCATC]TGACATAAAAGTATC | 84669 |
rs757750858 | snp | G/T | 1.64743e-05 | 0.00287 | missense | USP32 | GRCh38.p7 | 17:60198314 | GGGCTCGCTAACCGG[G/T]ATACTTGAATCCAAA | 84669 |
rs757757927 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60321962 | CCCTTTGCAATAAAG[A/T]GCCCATAGCTGGCAT | 84669 |
rs757763614 | snp | G/T | 3.34079e-05 | 0.00408691 | missense | USP32 | GRCh38.p7 | 17:60226223 | CTCAATTACCACAGG[G/T]TTGGCATCCTAAAAT | 84669 |
rs757787405 | in-del | -/AATAAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60358584 | GTCTCAAAAAAACAT[-/AATAAA]AATAAAAATAAAGGT | 84669 |
rs757813118 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60199929 | GGCCAGGTGCAGTGG[C/T]TCATGCCTGTAATCC | 84669 |
rs757832810 | snp | C/T | 1.72644e-05 | 0.00293801 | synonymous-codon | USP32 | GRCh38.p7 | 17:60211115 | CATACCAATGGGATT[C/T]GTCCTAGAAGTTTGA | 84669 |
rs757844115 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256437 | ATAAGGTTTTTGTTT[C/T]TTTTCCACCCAAATC | 84669 |
rs757856104 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60335129 | TACAGGCGTGCAAGA[C/T]ACCCAGCTAATTTTT | 84669 |
rs757879989 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60316725 | GGGCGCCTGTAGTCC[C/T]AGCTACTCGGGTGGC | 84669 |
rs757907081 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205585 | CATTCCATTGGGGAT[A/G]AATATTGGTCGGGGT | 84669 |
rs757909051 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353451 | CTCCTCCATTTTAAT[G/T]TAGATAGAGGCCAGT | 84669 |
rs757910939 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60333432 | GGTGAAACCCCCATC[C/T]CTACTACAAATACAA | 84669 |
rs757924965 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245327 | CATTGGGATTGGTGA[C/T]TCTGATGGCCAGCTG | 84669 |
rs757925746 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60298435 | AGTTGACACATATAA[C/T]CTATCCACATCCTCC | 84669 |
rs757928692 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60195630 | GGCATGAGCCACTGC[A/G]CCCAGCCTCAATCTC | 84669 |
rs757933022 | snp | A/G | 0.00334189 | 0.0407404 | synonymous-codon, intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422622 | TGGGCAAGGGGGTGA[A/G]GGGGACAAGCCACTA | 84669 |
rs757940959 | snp | A/G | 3.29495e-05 | 0.00405877 | missense | USP32 | GRCh38.p7 | 17:60183338 | TGCTGGCAGAGAGCC[A/G]GGTCTCTTGGTACCA | 84669 |
rs757949150 | snp | A/C | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422487 | CTCCGAGTTCTGGAG[A/C]CAAACCGCCCACTCC | 84669 |
rs757949293 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60396882 | CCCTTCTCTACTCCA[A/G]CTGCAATGAAGTTAT | 84669 |
rs757952184 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60391160 | CATTTCATGGAGAGG[G/T]ATGGAGCGAGAACTG | 84669 |
rs757957822 | snp | C/T | 1.64974e-05 | 0.00287201 | intron-variant | USP32 | GRCh38.p7 | 17:60223619 | GATAGAATCTCTTAT[C/T]TTTAGTTATTATACA | 84669 |
rs757959164 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60318258 | GCATATATAAAGATA[G/T]AGAAGAAGATCAAGC | 84669 |
rs757959580 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60363779 | GCTGAGATTATACAC[-/G]TGAGCCACTGTGCCT | 84669 |
rs757959694 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60261514 | AGCCAGGTGTGGTGG[C/T]GCAAGCCTGTAATCC | 84669 |
rs757960222 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60209259 | TTCATTCATTTTTGC[-/A]GTAAAGTTCTGATCT | 84669 |
rs757967352 | snp | C/T | 0.000131915 | 0.00812036 | missense | USP32 | GRCh38.p7 | 17:60223532 | TTATTGTCAGAAGTG[C/T]TATGTTGTCGAGCAA | 84669 |
rs757974815 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60229845 | TTGAGACAGAGTCTC[A/G]CTTTGTTGCCCAGGC | 84669 |
rs758020053 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60298014 | TTACAGAGGCTGCTC[A/G]CTTGACTGCCTTGCT | 84669 |
rs758049454 | snp | G/T | 7.27392e-05 | 0.00603028 | intron-variant | USP32 | GRCh38.p7 | 17:60255308 | TTTTTCTTTTTTTTT[G/T]TTTTTTTGAGACGGA | 84669 |
rs758066931 | in-del | -/AGAG | | | intron-variant | USP32 | GRCh38.p7 | 17:60333005 | TATTTCTATTTTGAA[-/AGAG]AGAATGTCAAAGAAA | 84669 |
rs758081225 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60196148 | GGCATGCACCTGTAC[C/T]CCCAGCTACTTGGGA | 84669 |
rs758084341 | snp | A/C | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420690 | CAACAAACAAACAAA[A/C]AAAAAAACCTCTTTC | 84669 |
rs758087735 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403265 | TCGTGATCTGCCGGC[C/T]TCGGCCTCCCAAAGT | 84669 |
rs758100239 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60238100 | ATTCTAATAATCTTA[C/T]TGAGAAGTAGAATTT | 84669 |
rs758108145 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60362568 | TGTTGTATACTTAAA[C/T]GCTGCAGGAGAGTCT | 84669 |
rs758112992 | snp | C/T | 1.77385e-05 | 0.00297808 | intron-variant | USP32 | GRCh38.p7 | 17:60183469 | CTGGAGAAGTAAAGG[C/T]AGAAAACATCTGCAT | 84669 |
rs758124731 | snp | G/T | 1.65641e-05 | 0.00287781 | intron-variant | USP32 | GRCh38.p7 | 17:60190721 | CAGAGGAAGAAATAA[G/T]TATGAAGGAATCTAA | 84669 |
rs758132726 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60343388 | TTATTCTAAAATTGA[C/T]CACATAATTAGAAGT | 84669 |
rs758141190 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60179860 | TACTTTTAGTAAAGG[C/T]GGGGTTTCACCATAT | 84669 |
rs758145711 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60367373 | CAATTGGCAGGGCGT[A/G]ATGGCTCATGCTTGT | 84669 |
rs758147885 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60307797 | CACCCTGGCCTGCCA[C/G]GCCCCCAAGGTGTGC | 84669 |
rs758165446 | in-del | -/AA | 3.3279e-05 | 0.00407902 | intron-variant | USP32 | GRCh38.p7 | 17:60192948 | GAAACAGAAGAGAAC[-/AA]AAAGAGTGTAAGAAG | 84669 |
rs758167015 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60381704 | TTCTAGATCTTGAAA[C/T]GTTCTGCATTTCCAC | 84669 |
rs758168502 | snp | C/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405269 | GTGCAGTGGCTCAAT[C/G]TCGGCTCACCACAGC | 84669 |
rs758171211 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60195270 | AAACGACTATCACTC[C/G]TTTCCTGAAATACTT | 84669 |
rs758193917 | snp | A/G | 3.42015e-05 | 0.00413516 | intron-variant | USP32 | GRCh38.p7 | 17:60301753 | CATTTCAGTTGTTGA[A/G]GAATCTGAGGCAGCT | 84669 |
rs758194157 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60272094 | TGTTGGGATTATAGG[-/T]GTGAGCCACTGTGCT | 84669 |
rs758195418 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60239526 | TTTCTTTCTGCTCCT[C/T]AGTCAATAATTTCAA | 84669 |
rs758201889 | snp | C/G | 1.65162e-05 | 0.00287365 | missense | USP32 | GRCh38.p7 | 17:60219712 | GTGTCCGAGTGGCAG[C/G]CTGCTGTCTCAGGAA | 84669 |
rs758206642 | in-del | -/CTGAGGAAC | 6.38794e-05 | 0.00565116 | intron-variant | USP32 | GRCh38.p7 | 17:60252337 | AACCAATATATTTCA[-/CTGAGGAAC]AGTATGTGAAATTTC | 84669 |
rs758224514 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60291807 | ACATGAGCTTCACAT[C/T]TCTTTGATCTTTTCT | 84669 |
rs758241208 | snp | A/G | 3.3295e-05 | 0.00408 | intron-variant | USP32 | GRCh38.p7 | 17:60271499 | AAGGGTCAAATCAAA[A/G]AAGATTATAAAACCT | 84669 |
rs758277230 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60391754 | CACACTCCCCAAGGC[C/T]GGCCGCCTTTCCCTT | 84669 |
rs758292748 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60224558 | GGGAGGCCAAGGCTG[A/G]AGGACTGCTTGAAGC | 84669 |
rs758293266 | in-del | -/TC | | | intron-variant | USP32 | GRCh38.p7 | 17:60239506 | TTCATTTTTCGTCAT[-/TC]TGTTTTCTTTCTGCT | 84669 |
rs758305499 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60274929 | TCAGACCATCCAAAC[C/T]ACACCACCTTCAAAG | 84669 |
rs758321721 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60327413 | TGTGGGTTGGTGGGG[A/G]GCGGGGGGGAGGCGG | 84669 |
rs758326250 | snp | A/G | 1.74476e-05 | 0.00295356 | intron-variant | USP32 | GRCh38.p7 | 17:60213566 | TTAATATAGATGCAT[A/G]CTTCCATCTTGTACC | 84669 |
rs758329520 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60313213 | CCAAGATCGCACCAC[C/T]GCATTCCAGCCTGGG | 84669 |
rs758344057 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60401878 | ATCTAAGGGAGCAGC[C/T]AGTAGATACAAAGTT | 84669 |
rs758357327 | snp | A/C | 1.64735e-05 | 0.00286993 | missense | USP32 | GRCh38.p7 | 17:60181425 | GCTGACCATTGCTGT[A/C]GCCATTGCCACATGC | 84669 |
rs758374503 | in-del | -/ACTAT | 4.94654e-05 | 0.00497295 | intron-variant | USP32 | GRCh38.p7 | 17:60222398 | TATAAGGCACTATTA[-/ACTAT]ACTTACTGGTCTAGG | 84669 |
rs758387889 | snp | A/C | 1.6522e-05 | 0.00287414 | missense | USP32 | GRCh38.p7 | 17:60212063 | TATTTGCTATAAAAG[A/C]CATCTCCTCAGGCCA | 84669 |
rs758388174 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60279112 | ATACAAGCTTTCTGA[C/G]TCAACATCATCATCG | 84669 |
rs758400411 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60390419 | ACAGCATCCCGGAAA[C/T]GACTAGCCTACTAGG | 84669 |
rs758417680 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60193842 | TCCAGTGAATGATCA[C/T]TGATAGCCTGTACTG | 84669 |
rs758419623 | in-del | -/ATAGGAAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60235559 | TTTTCGTTAGTGATC[-/ATAGGAAA]ATTTGGCAATGAGTG | 84669 |
rs758420893 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60278210 | CACCCAGACAATAAA[A/T]AAAAATTTTAAAAGC | 84669 |
rs758420996 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60292718 | CCTGGATTATTCAGA[A/T]ACCTCAATTGGACTC | 84669 |
rs758427683 | snp | C/T | 1.65378e-05 | 0.00287552 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269502 | TGATAACCCACAGGA[C/T]ATCTCCTTAAAATCT | 84669 |
rs758432644 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60287895 | GAGGCGTGTGGATCA[C/T]GAGGTCAGGAAATCG | 84669 |
rs758441731 | snp | C/T | 4.94303e-05 | 0.00497119 | missense | USP32 | GRCh38.p7 | 17:60181514 | AACTCTGGTTGGCTG[C/T]CCCCCAGCACATGCC | 84669 |
rs758479132 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60200132 | GCAGGAGGCATAGAG[C/T]ACAGTGAGCCGAGAT | 84669 |
rs758491894 | snp | C/T | 1.64779e-05 | 0.00287031 | missense | USP32 | GRCh38.p7 | 17:60183233 | AGCACGTCCTCTTCC[C/T]CAGCCGAACTCTGCG | 84669 |
rs758513771 | snp | C/G/T | 0.000277203 | 0.0117698 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391966 | CCCCTCGGCGGGGGG[C/G/T]CGGAGCCTGATCTCG | 84669 |
rs758517796 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60324014 | GGCCAGGTGCAGTAG[C/T]TCATGCCTGTAAAAC | 84669 |
rs758528054 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60368991 | TTATTTTTTAAAAGA[-/T]TTTTTTTTTTTTTTT | 84669 |
rs758531745 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60417113 | AGTAGAGACTGGTTT[G/T]AACCGTGTTGGCCAG | 84669 |
rs758533801 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60400792 | TTGGGATGCTGAGTC[A/G]GGGGGATCACTTGTG | 84669 |
rs758547386 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60184390 | TTCCCTCTAGTTCCT[A/G]TCTGTGGAGCTAGCT | 84669 |
rs758575426 | in-del | -/AAAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60390132 | ACTGTATAAGAAATT[-/AAAC]AAAAACCTTCCAGTC | 84669 |
rs758577749 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60204761 | GATGTGAGCCACCGC[A/G]CCTGGCCATTTTCTT | 84669 |
rs758577802 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60236336 | TATAAGGAAAACCGC[A/G]AAACATTTAGATGTA | 84669 |
rs758590351 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60386727 | CAGTTTGGTAAATGG[C/G]GAGCTCACTAACCAG | 84669 |
rs758599023 | snp | C/T | 2.54314e-05 | 0.00356582 | intron-variant | USP32 | GRCh38.p7 | 17:60208615 | TAAATAAAGTAAATT[C/T]AATGGAGTCAAGTAA | 84669 |
rs758599108 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60339220 | CCAGCCTAGAAGAAC[A/G]TAAAAATATTAAGTA | 84669 |
rs758606826 | snp | C/T | 1.64789e-05 | 0.0028704 | missense | USP32 | GRCh38.p7 | 17:60208174 | ATATTCAGTCTTAGT[C/T]CATACCGTACAGGGG | 84669 |
rs758609282 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60289068 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 84669 |
rs758618687 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60285581 | CTGCCGGAAAGGATC[C/T]TATGAGTTAGGAGAC | 84669 |
rs758631539 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60317936 | ATTGCAGTAAGCTGA[A/G]ATGGTGCCACTGCAC | 84669 |
rs758632320 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60289398 | TGCCTGAGTTACTAT[A/G]TCTTAATTAAATCTG | 84669 |
rs758633535 | in-del | -/AAAAA | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413479 | ATATTATTTTGACTT[-/AAAAA]GGAAGGGAGGACAGG | 84669 |
rs758638741 | snp | C/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403196 | TTTGTATTTTTAGTA[C/G]AGACAGGGACAGGGT | 84669 |
rs758681505 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410511 | GTCTCTACTAAAAAT[A/G]CAAAAAATTAGCTGG | 84669 |
rs758718794 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60250843 | CTACATGAGACTAGA[A/G]TTTTATGAAAGCAAC | 84669 |
rs758721734 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60387699 | CTCCCAATAAACCCA[A/T]CATAAGTTGAAAATA | 84669 |
rs758742305 | snp | A/G | 1.64933e-05 | 0.00287165 | intron-variant | USP32 | GRCh38.p7 | 17:60180651 | CACTGTAAGAGATAA[A/G]AGAGTGGAGGTATGT | 84669 |
rs758763551 | snp | A/T | | | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402107 | TAGGTCACTGTGTGC[A/T]TGTATTAGCTGCACC | 84669 |
rs758772442 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60210904 | ATACCAAGTGAAGGA[C/T]CCAAAAACATTTATT | 84669 |
rs758781364 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60181907 | TATTATGTAGCCAGT[A/T]AGTTACATTTTTGTC | 84669 |
rs758783136 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295258 | AAAAAAAAAGATAAA[-/TT]TGTCTGTCAACAAGA | 84669 |
rs758797697 | in-del | -/CTTC | | | intron-variant | USP32 | GRCh38.p7 | 17:60330453 | TCTTTCTTTTCTTTT[-/CTTC]CTTCCTTCCTTCTTT | 84669 |
rs758798473 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60310475 | GGAGGCTGAGGTGGG[A/C]AGATCATGAGGCGAA | 84669 |
rs758804436 | in-del | -/TT | | | intron-variant | USP32 | GRCh38.p7 | 17:60191998 | TTAGAACTGGCAAAC[-/TT]ATATTTAACGAGAGG | 84669 |
rs758807038 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60323915 | TTCAAAGATGGAATA[C/T]TAGTAAAGTTGCCAC | 84669 |
rs758815723 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60296797 | GCCTCATATAAAATG[C/G]CATGGTATTTTGTAC | 84669 |
rs758826299 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60274565 | AAACAAAAGAACTAA[G/T]ATAATAATTTATCTC | 84669 |
rs758851473 | snp | A/G | 1.65373e-05 | 0.00287548 | missense | USP32 | GRCh38.p7 | 17:60301641 | TTGTAAGGAGGACAA[A/G]TCCAACTATTAAATT | 84669 |
rs758872904 | snp | C/T | 1.78128e-05 | 0.0029843 | intron-variant | USP32 | GRCh38.p7 | 17:60183140 | AGTCCCAAGAAAGCA[C/T]CTGCATAAGGCCCCC | 84669 |
rs758876671 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411282 | TGAGCCGAGATTGCC[C/T]GATTGCACTCCAGCC | 84669 |
rs758878831 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60369723 | ATAGTTGATTAAATT[C/T]AAGGTACTTATTAAG | 84669 |
rs758887368 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409969 | GGTTTAAAACAAAGA[C/T]GAAAATAGCCCCTTC | 84669 |
rs758890591 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60204186 | CTCTAAGAAAAAAAA[-/C]AAAACAAAACAAAAA | 84669 |
rs758891943 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60394238 | GCAGAGTGCGAGTTC[C/G]GAGTTAGATTATCGT | 84669 |
rs758893607 | snp | C/T | 5.33898e-05 | 0.00516644 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231634 | ACCCCCCAAAGCCCA[C/T]GGGAGAGAGGCACGA | 84669 |
rs758914635 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404510 | CAAGAAGACAATCTC[A/G]TTTCCTAAAAGAACT | 84669 |
rs758926881 | snp | G/T | 3.29669e-05 | 0.00405984 | intron-variant | USP32 | GRCh38.p7 | 17:60198451 | TGTCCTCATCTGTAT[G/T]TACAAACAAGAGAAT | 84669 |
rs758942956 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60187607 | GCCAACCACAAATTA[C/G]AGTAAGCTAGTAAAG | 84669 |
rs758953059 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60350357 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT | 84669 |
rs758972739 | snp | A/G | 3.35036e-05 | 0.00409276 | intron-variant | USP32 | GRCh38.p7 | 17:60192816 | AGCTGAAATTCTACT[A/G]AAGTAATTCTTTTGC | 84669 |
rs758985001 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60357340 | CGCCTATGGTTCCAG[C/T]TACACGGGAAGCCAA | 84669 |
rs759034694 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60248310 | CTTCTTCCTTTGTCT[G/T]TAGTTTTCAACACTT | 84669 |
rs759040324 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60384791 | AGCAAAACTCCGTCC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs759061272 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283638 | AAAATACTATCAACC[A/T]GGATATAAAACACAG | 84669 |
rs759064994 | snp | C/T | 3.6167e-05 | 0.00425232 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231505 | ATTCCTTTTATTTCC[C/T]ACTCAACTACACATG | 84669 |
rs759067659 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416387 | GATTATGAAACAGGC[A/G]TATGCCATCAAAGAG | 84669 |
rs759072707 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60199377 | TTAAAATTTGCTTTG[A/C]GTACGTTAAAGAGAT | 84669 |
rs759084484 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60317289 | GAGGCCAAGGCACAA[-/G]GATCACTTGAGCCCA | 84669 |
rs759093326 | in-del | -/ATTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60382867 | ACTAATCTCACAGGA[-/ATTT]ATTTATCAGCTTCAA | 84669 |
rs759097644 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60302153 | TTTATTTATTTATTT[A/G]AGATGGAGTTTTGCT | 84669 |
rs759123722 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60179569 | TTGGCTGTCTCACAC[C/T]TGCCCCTTTAAGATG | 84669 |
rs759150471 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60233902 | TCTCTCCATATAAAG[C/T]GATACTCCTCTCCTC | 84669 |
rs759152917 | snp | A/C | 1.65051e-05 | 0.00287267 | missense | USP32 | GRCh38.p7 | 17:60226197 | TTTCCTCCATTCAAA[A/C]CAGATGATGGCTCAA | 84669 |
rs759155086 | snp | A/T | 1.69919e-05 | 0.00291473 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266138 | CATTTTTGTATTCTG[A/T]GGTATAATATATTTT | 84669 |
rs759165489 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60321366 | ACTGGTGGGAACTGA[G/T]GCCCTGAGCCCATCA | 84669 |
rs759167463 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60315420 | TCAAAAAATAAAAAT[A/T]AATAAAATAAAATGA | 84669 |
rs759174208 | snp | A/G | 3.53951e-05 | 0.0042067 | intron-variant | USP32 | GRCh38.p7 | 17:60208045 | CAAAAGTTTCTTAGA[A/G]TAGTTAATATTACCT | 84669 |
rs759185537 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60301403 | ACTCTAGTAGGTGTG[A/C]AGTAGTATCTCACTG | 84669 |
rs759191316 | snp | C/T | 1.65012e-05 | 0.00287234 | missense | USP32 | GRCh38.p7 | 17:60255201 | GGTTCAAAAACTCAT[C/T]GGCAAGAACATTTTT | 84669 |
rs759194383 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60348464 | GACTTATCAAGTTAA[-/G]GCAGAAAGGACCAGC | 84669 |
rs759198726 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60224695 | GGCTAAGACAGGAGG[A/G]TCATTTGAGCCCAGG | 84669 |
rs759199768 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60368551 | AAACGAGGGGAAAAT[A/C]TATTTAAACTGAGGT | 84669 |
rs759209642 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60385955 | AATTCTGGTCATCTT[C/T]GAATAGATACATCTT | 84669 |
rs759226834 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60401244 | GCGTGGTGGTGGGCG[A/C]CTGTAGTCCCAGCTA | 84669 |
rs759249062 | snp | A/T | 1.64757e-05 | 0.00287012 | missense, utr-variant-5-prime, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266031 | AGTGCAACCACCATG[A/T]CTCTCAGTTCAACCC | 84669 |
rs759251246 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60387197 | CATAGGTAGTATAAA[A/T]CTAACGAAATTTTAA | 84669 |
rs759255440 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60281709 | AAATCTATTTCCCAC[A/C]GCAATAGTAAGTGGC | 84669 |
rs759268002 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60309776 | GCAGACTGGGCACAG[G/T]GGCACATACCTGTAA | 84669 |
rs759302259 | snp | C/T | 3.303e-05 | 0.00406373 | intron-variant | USP32 | GRCh38.p7 | 17:60214808 | CAGTAAGAAAAAAGG[C/T]AGATGTGAAAAAGAA | 84669 |
rs759310169 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60238371 | TATCTCTTGATGTAT[-/AA]AAGTTTTAAGTTTTG | 84669 |
rs759330501 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | USP32 | GRCh38.p7 | 17:60198355 | TAGGTCTTTCTTCCG[A/G]GTATGCACAGTACAT | 84669 |
rs759332904 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60394572 | ATGACCGCATGTGTC[A/G]TTTTCCAATGGGGTG | 84669 |
rs759355998 | snp | A/C | 2.82267e-05 | 0.00375667 | intron-variant | USP32 | GRCh38.p7 | 17:60301549 | CAGAATTTTGAGATA[A/C]ATTATTCTGTACATA | 84669 |
rs759358415 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60348973 | TATTAACATTTGCAA[C/T]TGAAGGAGGTAACTT | 84669 |
rs759359641 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312876 | ACATAAGGCCCATGG[C/T]ATATGAATACATTAA | 84669 |
rs759377224 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366977 | TACAGGAGCCCGCCA[C/T]CACACCCAGCTAATT | 84669 |
rs759382592 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60222591 | GACTTTCAATATTAC[-/AA]AAGTTTTTGGGTCTC | 84669 |
rs759384925 | in-del | -/ATC | 1.64866e-05 | 0.00287106 | cds-indel, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265982 | ATAACTTACAGGAAT[-/ATC]ATCAGTGCGGTTGTC | 84669 |
rs759443493 | snp | A/C | 1.65285e-05 | 0.00287471 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60294738 | TCCACCACGTGGAGC[A/C]TTCTTTCCATTTCTT | 84669 |
rs759455542 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409154 | GGACTTCAAGACCAC[A/C]CTGAGCAACATGGCG | 84669 |
rs759475592 | snp | C/G | 3.2969e-05 | 0.00405998 | missense, intron-variant | USP32 | GRCh38.p7 | 17:60288576 | GTATCACTATCATCA[C/G]TGAGGGTAACATACA | 84669 |
rs759518992 | snp | A/G | 2.70391e-05 | 0.00367679 | intron-variant | USP32 | GRCh38.p7 | 17:60206997 | AAGGAGCAATCATGA[A/G]AAGGAGTTCTAGTTC | 84669 |
rs759519638 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60351289 | CTTTTAGCAACTCCC[A/G]GGCTCAAGTGATCCT | 84669 |
rs759531107 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60252721 | AGGGGAAGACATTAC[C/T]TCAGGAACAGATTTC | 84669 |
rs759559983 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60364182 | TGGGGCAAAGCAAGT[C/T]CTCTCAGGCCTCTTT | 84669 |
rs759589184 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60258595 | TAGGGTGTTGTATAC[G/T]TAGAAAGTAACAGCT | 84669 |
rs759600168 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | USP32 | GRCh38.p7 | 17:60236139 | GGAATCTAACTCACG[C/T]ATTTGACATATTCTT | 84669 |
rs759621384 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60361756 | TCCACTTATCCTGTC[A/G]TTCAGAAGGTATAAA | 84669 |
rs759625690 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195818 | TGATGACATCTGTAT[C/T]TCCAGCAGAGGACAT | 84669 |
rs759627886 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60319346 | CGAGTATAATAAACA[C/T]TTAGATAGAAAGTAC | 84669 |
rs759628542 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60270737 | CTGAGATAGGAGAAT[C/T]GCTTGAACCCAGGAG | 84669 |
rs759631118 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60267359 | CAGTGATCCAAGATC[A/G]TGCCCCTGCACTCCA | 84669 |
rs759636610 | snp | G/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422171 | CTGTGCTTTCCTCTC[G/T]GGGAGCCCCCACCAC | 84669 |
rs759668248 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60285431 | AGCTGGTGTGTAATC[C/T]GTAGTCAAGTTATAT | 84669 |
rs759669513 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60382840 | TGTTCATAAGTACAA[C/T]ACTTACCCCATACTA | 84669 |
rs759675137 | snp | C/T | 1.6759e-05 | 0.00289469 | missense | USP32 | GRCh38.p7 | 17:60183416 | TGTGATTTTATCCAC[C/T]GACCATTTACAAATT | 84669 |
rs759691854 | snp | A/T | 1.65296e-05 | 0.00287481 | synonymous-codon, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271456 | CCAATAGCGTTTCTC[A/T]AGATCAATGATGTCT | 84669 |
rs759713172 | in-del | -/AAAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60399665 | AGACCCTGTCAAAAT[-/AAAT]AAATAAATAAATAAG | 84669 |
rs759719840 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60344827 | ACTACAAAATAGTAA[A/G]CTTTTATTTTATTTT | 84669 |
rs759741230 | snp | A/C | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423099 | TACTTTTCTGAGAAG[A/C]TTTTGAAAGGTGAGG | 84669 |
rs759752386 | snp | G/T | 1.65097e-05 | 0.00287308 | intron-variant | USP32 | GRCh38.p7 | 17:60226034 | GGGGAATAGGTCATA[G/T]TTACCGCTGCCAGCA | 84669 |
rs759753067 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312522 | CCTTGACCTCCCAGG[C/T]TCAAGTGATCCTCCC | 84669 |
rs759765849 | snp | C/G | 1.67961e-05 | 0.00289789 | missense | USP32 | GRCh38.p7 | 17:60185474 | CCAGGATGGGTGGAA[C/G]CCTCCAGAGATCCAG | 84669 |
rs759799219 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | USP32 | GRCh38.p7 | 17:60209488 | AAAGCCAGAAGTTCT[C/T]GGGAGTCCTGTTGCT | 84669 |
rs759812109 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60290987 | AATGTTTACAATGTC[C/T]TAAGAACTGCTCTAA | 84669 |
rs759824012 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179188 | TTCAGTGACGCTTTT[A/G]CCAAATGTCAGCTAC | 84669 |
rs759825674 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60197297 | GAACTCTCATTTGTA[A/C]CATGATGGCAAGAAA | 84669 |
rs759846610 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60271132 | TACATGAGCATGCTC[A/G]GGTGCAGAGAGCTAA | 84669 |
rs759850539 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60247188 | ATCCATTTTCTTTTC[-/T]TTTTTTTTTGAGGCG | 84669 |
rs759865691 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60307285 | TTTGTATTTTTAGTA[G/T]AGATGGGGTTTCACT | 84669 |
rs759869221 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405042 | AATTAGCCGGTATGG[C/T]GCTGCACAGCTACTC | 84669 |
rs759875673 | snp | A/C | 3.41676e-05 | 0.00413311 | intron-variant | USP32 | GRCh38.p7 | 17:60391854 | CGCGGGCCTCCCAGG[A/C]AGCTCGCCCAGACCC | 84669 |
rs759878294 | in-del | -/GAA | 8.94847e-05 | 0.00668837 | cds-indel | USP32 | GRCh38.p7 | 17:60181736 | CCACTTTTTCTTGAT[-/GAA]GAAGGAGAACCTGTG | 84669 |
rs759892851 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60220441 | AACCAGTCTGTTCAC[-/AT]ATGTTTTGTCTATGA | 84669 |
rs759916094 | in-del | -/T | 1.67147e-05 | 0.00289086 | intron-variant | USP32 | GRCh38.p7 | 17:60210964 | AGAGAAAAATGATTA[-/T]AACAACTATTAGGAA | 84669 |
rs759938177 | snp | A/T | 2.14719e-05 | 0.00327651 | intron-variant | USP32 | GRCh38.p7 | 17:60219819 | TAAAAAGAGATCACT[A/T]AAAAAAGAAACAAAA | 84669 |
rs759948291 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60345890 | GGGAGGCTGAGACAC[A/G]ATAATCACTTGAACC | 84669 |
rs759966874 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414977 | CTACCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC | 84669 |
rs759967789 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60240581 | GTGCTGGGGCATTCC[C/T]ACAATGGTTTACAAC | 84669 |
rs759971020 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60263673 | TACACAAGGCATTTT[C/G]TAACAGAAACTTTTC | 84669 |
rs760006695 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60391455 | GCAGCCGCCTCCTCG[A/T]CCCCTTCCAGCTAAG | 84669 |
rs760011282 | in-del | -/AAAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60376422 | GAAGCTGATTTTTAA[-/AAAT]AATAAATATTAATTT | 84669 |
rs760022604 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60247421 | CTGGCCTCAGGTGAT[C/T]CAGCCGTCTCGGCCT | 84669 |
rs760036893 | snp | C/T | 3.32535e-05 | 0.00407746 | intron-variant | USP32 | GRCh38.p7 | 17:60212137 | TTAATTTCTTATCTA[C/T]CTAATTTATACCCAT | 84669 |
rs760043060 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191184 | AGGTGGGTGGATCAC[C/T]TGAGGTCAGGAGGTC | 84669 |
rs760049265 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245925 | AATAGTATATGTTTT[G/T]GGGGTACATGTGATA | 84669 |
rs760076983 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60290090 | CAGAGTCAACAGGCC[C/T]GGGGTAGAAAGCATT | 84669 |
rs760087996 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60355421 | CCTGTAAGGAGACCG[A/T]TTGCCGGAATGGTAA | 84669 |
rs760112925 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60374110 | AATCGCTTGAACCAG[A/G]GAGGCGGAGGTTGCA | 84669 |
rs760113729 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60277363 | CAGTAACACATTTCT[C/T]TAACATTTTTGAAAA | 84669 |
rs760136044 | snp | C/G | | | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402883 | TCAGCTAAGGCCTTA[C/G]CTGGAGTTGTCATAA | 84669 |
rs760146432 | snp | C/T | 1.77492e-05 | 0.00297898 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231591 | GAGGGCTGCTCTTGG[C/T]CTCCAGCCTTGGCTA | 84669 |
rs760149323 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60303108 | CTCTAGTGCCAGTGA[C/T]AACTCAACCCAGCAA | 84669 |
rs760160278 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60225045 | TGTGGGGTGCATTTA[A/T]TTTAATTATGTTTAT | 84669 |
rs760166362 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60373126 | TGAGCCCAGGAGCTC[A/G]AGGCTACAGTAAGCC | 84669 |
rs760167451 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60235742 | TCAGTCCTTCGGTTT[A/G]ATCCCAGATCTTCCA | 84669 |
rs760168016 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393088 | TTTTTCATCTTGCAA[A/C]AGGGAAACTCTGTGC | 84669 |
rs760194721 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60342259 | AACAGCAAATATTGC[A/T]GAACAGCAAATATTG | 84669 |
rs760197428 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60187251 | CAAGGCTGGATTTGA[G/T]CGTGCAATTAAGGTT | 84669 |
rs760200800 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60401349 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 84669 |
rs760206117 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60386165 | ATTATTAAATGAGAG[G/T]ACTTATTGGAATGCA | 84669 |
rs760244010 | in-del | -/TCT | | | intron-variant | USP32 | GRCh38.p7 | 17:60237121 | AATCTACTCTATCTA[-/TCT]ATCTATCTATCTATC | 84669 |
rs760256168 | snp | C/T | 1.73e-05 | 0.00294104 | intron-variant | USP32 | GRCh38.p7 | 17:60208246 | TTTATTGGTAAAATG[C/T]AGGTTTCATTGAAAG | 84669 |
rs760275237 | snp | C/T | 1.64822e-05 | 0.00287068 | missense | USP32 | GRCh38.p7 | 17:60192883 | GAGTTCCCATCTTTC[C/T]GCACAACTCGTAGAG | 84669 |
rs760288653 | in-del | -/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403020 | GTAAGCCGTATCTCT[-/G]TTTTTTTTTTGAGAC | 84669 |
rs760294265 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60288769 | AAATTTGCAATTAGT[C/T]GGCAATTACCTTTCT | 84669 |
rs760296239 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60348046 | AGAATGGCGTGAACT[C/T]GGGAGGCGGAGCTCG | 84669 |
rs760299694 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60221460 | ACAAAACCTTCCTGG[A/C]ATAAGGAAGTTTTAG | 84669 |
rs760305171 | snp | A/C/G | 0.0124562 | 0.0779302 | synonymous-codon, missense | USP32 | GRCh38.p7 | 17:60214719 | CTGCATTCGACTAAA[A/C/G]CAGCCTGTATAGGCT | 84669 |
rs760329098 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60221814 | AATATACCAAAACAA[A/T]TCCCACCAAAACATC | 84669 |
rs760344082 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60258686 | TAATGCAAGAGAACA[A/C]TTCGCTGTTTTACAG | 84669 |
rs760365245 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60237245 | TCCTGGGCTCAAGCA[A/G]TCCTCCTGCCTCAGC | 84669 |
rs760366174 | snp | C/T | 1.78797e-05 | 0.0029899 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231519 | CCACTCAACTACACA[C/T]GTCTGAGGCAGGAAA | 84669 |
rs760379438 | in-del | -/TA | | | intron-variant | USP32 | GRCh38.p7 | 17:60336208 | CCCATTACGCTTAAC[-/TA]TATGTTAGATCTTCT | 84669 |
rs760402911 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181393 | ATCAGTGCTGTCTTC[C/T]TCACTGTGGTTTCCA | 84669 |
rs760404570 | snp | C/T | 4.95921e-05 | 0.00497932 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265429 | TTGTGGTGTCATGTG[C/T]ATTCAGTATGCCTTC | 84669 |
rs760431965 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60275232 | GAGGCCAGGGCAGGC[A/G]GATCACCTGAGGTCA | 84669 |
rs760453737 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60391334 | CAAACGGTGAAGGGT[G/T]GCAGAAGCGGATGGC | 84669 |
rs760479756 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60370899 | CCAGGAGTTTGGGAC[A/C]AGCCTGAGCAACATA | 84669 |
rs760491545 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230562 | GTAATAACCTTTAGA[C/T]TTGGAGAATATGGGC | 84669 |
rs760492357 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60344862 | AGAGACAGTGTCTCA[A/C]TATGTTGCCTAGACT | 84669 |
rs760496536 | snp | C/T | 0.000206676 | 0.0101634 | intron-variant | USP32 | GRCh38.p7 | 17:60255300 | ACATCTTTTTTTTCT[C/T]TTTTTTTTTTTTTTT | 84669 |
rs760503803 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60334429 | GTTTCTAAGCCATGC[A/G]GCTCATCTGTGGCTT | 84669 |
rs760512213 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60379336 | GAAAACTTTGAAAAG[C/G]TGAAAAATCCACCTG | 84669 |
rs760513198 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60243657 | TAAGCCACTTAAAAC[A/G]GTAAAAACATTTTTA | 84669 |
rs760527677 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60351404 | TAGCTGATTTTTTTC[A/C]ACAAGCATTTATGAA | 84669 |
rs760528671 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412768 | ATGCATTTTTTTCCT[C/T]TCCAAAATCATTCCC | 84669 |
rs760533282 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296283 | CTGTGTATGTGAGAT[C/T]ATCTGGAAACAGAGT | 84669 |
rs760537139 | snp | A/G | 1.65307e-05 | 0.0028749 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183205 | GCTGAGTGAGGATGG[A/G]CTTTTGCTCAGGAGC | 84669 |
rs760567277 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60396434 | AGTACACAAGTATAT[A/G]ATGTAAAAGATCACT | 84669 |
rs760584698 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60350702 | ATCTTCTCTCTCTCC[-/C]TCTATCCCTCTCTCA | 84669 |
rs760631192 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183301 | CTCAGAGAGCTCATC[C/T]CCCTGGGGTGTGAGT | 84669 |
rs760638356 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60288312 | AGGCATGGTGGCGAG[C/T]GCCTGTAGTCCCAGC | 84669 |
rs760650133 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60398060 | AAGCTATAAAATAGC[A/T]TTTAGTTAAAATTGT | 84669 |
rs760650930 | snp | C/G | 1.65463e-05 | 0.00287626 | missense | USP32 | GRCh38.p7 | 17:60185632 | CGACTCTGCTCCACA[C/G]TCTCATGCTCATCTA | 84669 |
rs760653466 | in-del | -/CAAAA | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421990 | ATCTTTATACACCCC[-/CAAAA]CACACACATCCCACC | 84669 |
rs760727401 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60266955 | CACTGTGCCCGGCCA[A/C]TTTTTGTATTTTTAG | 84669 |
rs760730281 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60277910 | AAAAAATAACTTAAT[A/G]ATAGTTCCTTTTTTT | 84669 |
rs760742040 | in-del | -/GAGTTC | 0.00121583 | 0.024626 | cds-indel | USP32 | GRCh38.p7 | 17:60211042 | GGGCAACATTCTTCT[-/GAGTTC]CACTCCAAAGTTCCT | 84669 |
rs760753437 | snp | C/G/T | 1.65671e-05 | 0.00287807 | intron-variant | USP32 | GRCh38.p7 | 17:60222360 | AAAAGTAACAGAAGA[C/G/T]CCCCATCTATGACTG | 84669 |
rs760758461 | snp | C/T | 3.4638e-05 | 0.00416147 | missense | USP32 | GRCh38.p7 | 17:60211088 | ACCATAGCATTTAGC[C/T]ATATGCCCCTTCATA | 84669 |
rs760767751 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60346209 | CTTGGCCTCCAGAAA[C/T]GCTGAGATTAAAAGC | 84669 |
rs760768257 | snp | A/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406318 | CAAATAGCTGGGACT[A/T]CAGGCCCATGCCACC | 84669 |
rs760772723 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60241541 | TTTGTTCTTTATTTT[C/T]CAATGTTTCTGTGGA | 84669 |
rs760779381 | snp | A/T | 1.95865e-05 | 0.00312936 | intron-variant | USP32 | GRCh38.p7 | 17:60252366 | TCAACTATATAATTG[A/T]AACTACAAATTTACC | 84669 |
rs760792293 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60225666 | CTTAATAACTATCCA[C/T]GGGGAGGCCAGGCAT | 84669 |
rs760797502 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393333 | AATGAAAAGCAGGGA[C/T]GTGAACAGGTATTTG | 84669 |
rs760802270 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60255531 | TCTTGAACTCCTGAC[C/G]TCGTGATCCATCCGC | 84669 |
rs760808251 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60292033 | ACCAATGACCTACCT[-/G]CAGATCACCAAATTT | 84669 |
rs760818400 | snp | A/C | 1.66021e-05 | 0.0028811 | intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179454 | AAGAAAAACCTTTAA[A/C]AAAAAGCCATCACTA | 84669 |
rs760820853 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60365443 | CCAAGATCAGGCCAC[C/T]TGCAATCCAGCCTGG | 84669 |
rs760860374 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60328797 | AGAAGCTGCTTGAAG[A/T]GCACCTGGTCCAGCT | 84669 |
rs760865449 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60357701 | CAGGCTGAAGCTGAA[A/T]TAATCTCTGGAAAGG | 84669 |
rs760871572 | snp | C/G | 3.30453e-05 | 0.00406467 | synonymous-codon, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60294701 | TGAGAAACACTTCCT[C/G]AGTGTATCTGGGACT | 84669 |
rs760873312 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | USP32 | GRCh38.p7 | 17:60236271 | AAATTAAATACATCA[A/G]ACAAAGTGTGAAATA | 84669 |
rs760892624 | snp | A/C | 0.000132356 | 0.00813391 | intron-variant | USP32 | GRCh38.p7 | 17:60214607 | CTCTCTATGACTCTG[A/C]GATGCCTCTTACCTC | 84669 |
rs760908360 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60307544 | TCAAAAGACCCCAAA[C/T]AGCCAAAAAATCCTG | 84669 |
rs760923620 | in-del | -/TAATA | | | intron-variant | USP32 | GRCh38.p7 | 17:60349171 | ACAATATAATTAATC[-/TAATA]TATTAATTATATATT | 84669 |
rs760927531 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | USP32 | GRCh38.p7 | 17:60198387 | GAACAATCAATGGCA[C/T]TCCAAAGAGGCTGGG | 84669 |
rs760928438 | in-del | -/TTCT | | | intron-variant | USP32 | GRCh38.p7 | 17:60281021 | GAATAAATTTGTTGG[-/TTCT]TTGTTTTTATAGATT | 84669 |
rs760940595 | snp | C/T | 3.2956e-05 | 0.00405918 | missense | USP32 | GRCh38.p7 | 17:60205638 | TGAACATTTCATTTG[C/T]AGATGGCGAAGAGGA | 84669 |
rs760953687 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60279510 | AAAAAAACCTTATCT[A/G]TATTTCACAAGTAAT | 84669 |
rs760954627 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60374259 | ATCATCAATATCACT[A/G]TCTTCCACCTTCACG | 84669 |
rs760959071 | snp | C/T | 3.29663e-05 | 0.00405981 | synonymous-codon, intron-variant | USP32 | GRCh38.p7 | 17:60288602 | ATACACACCTCCAGA[C/T]AGAAGCCATCGAGAG | 84669 |
rs760995798 | snp | C/T | 5.00638e-05 | 0.00500294 | missense | USP32 | GRCh38.p7 | 17:60211376 | CTCCAGAAAGATTAC[C/T]TGTTGAGTTCATAAA | 84669 |
rs760999999 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60280844 | CAGACTGAGAATTTA[C/T]AGGTAATATAAATCA | 84669 |
rs761001502 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60391611 | CCCTGGACACATCCA[C/G]GATCACAACGCCACC | 84669 |
rs761027827 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60297518 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAACCTC | 84669 |
rs761043171 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60237878 | GGCTATTGTGAACAG[C/T]GGTACTATGAAAGTT | 84669 |
rs761050329 | snp | A/G | 1.69069e-05 | 0.00290743 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391957 | TCCCCTCATCCCCTC[A/G]GCGGGGGGTCGGAGC | 84669 |
rs761060688 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392648 | GAAAGGAGTGGGTAG[A/G]CAGGGAGCTCCCAAC | 84669 |
rs761083826 | snp | C/T | 3.29478e-05 | 0.00405867 | missense | USP32 | GRCh38.p7 | 17:60222512 | ATCAGCTGTGGAGTT[C/T]GTTTTAATCGTCCTC | 84669 |
rs761092910 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60218858 | CCTCAGCCTCCCAAA[-/T]TGTGGGATTACAGGC | 84669 |
rs761092951 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60313848 | AACAAAGACAACAAA[C/T]TCAGGTACTTATAAC | 84669 |
rs761101248 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60249840 | ACTCGGCCATTCCAG[A/C]AATCACGATACTTTT | 84669 |
rs761137621 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60226733 | AGATGAGTGGTGTAT[C/G]TACATAGAGTGAAGG | 84669 |
rs761140302 | snp | C/G | 1.69928e-05 | 0.00291481 | intron-variant | USP32 | GRCh38.p7 | 17:60391863 | CCCAGGCAGCTCGCC[C/G]AGACCCCTCCCCCCT | 84669 |
rs761150923 | snp | G/T | 1.65198e-05 | 0.00287395 | missense | USP32 | GRCh38.p7 | 17:60223418 | TTACTTACCTTTACT[G/T]GTTCTTGAGTTACTA | 84669 |
rs761157255 | in-del | -/T | 1.79355e-05 | 0.00299456 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231656 | AGGCACGAAAGGTGA[-/T]TTTAAAGTATCTTCT | 84669 |
rs761161634 | snp | C/T | 3.65344e-05 | 0.00427386 | intron-variant | USP32 | GRCh38.p7 | 17:60255304 | CTTTTTTTTCTTTTT[C/T]TTTTTTTTTTTGAGA | 84669 |
rs761165794 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60311412 | CAGACAATGATGTCA[C/T]CCCAGTAAATAATAT | 84669 |
rs761185600 | snp | A/G | 3.33678e-05 | 0.00408446 | missense | USP32 | GRCh38.p7 | 17:60207032 | TTACCTGTCTGTGTT[A/G]GACTAGAAGCTGAAA | 84669 |
rs761196336 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60276929 | TGTCAAAAGCAAGCT[A/G]AAGTAGATTACATAT | 84669 |
rs761229583 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60338867 | GTAATACATGGTTAC[A/G]ATTATAAGCAAGATT | 84669 |
rs761231024 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60310268 | AAGAAAGGAAATCAA[C/T]GTATCAAAAAGATAC | 84669 |
rs761231463 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60359594 | GATGAGAGGATCACT[C/T]GAGCCCAGGAGTTTG | 84669 |
rs761253176 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60302517 | TGAAATGCCTTTTCA[A/G]CTCACAATATTCCCA | 84669 |
rs761255529 | snp | C/T | 5.03157e-05 | 0.00501551 | intron-variant | USP32 | GRCh38.p7 | 17:60301728 | AGATGATAAAGCCAA[C/T]CTTAGGAGGCATTTC | 84669 |
rs761264854 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60371448 | GGCACACGCCTATAT[A/G]ATCCCAGCTACTCAG | 84669 |
rs761278201 | snp | A/G | 1.64814e-05 | 0.00287061 | intron-variant, missense | USP32 | GRCh38.p7 | 17:60219649 | GTAAATGCTGAGGAA[A/G]CATTCTCAGGCTCAT | 84669 |
rs761299930 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60329369 | CCACAGAATTGTTGA[C/G]TATTATATGCTAGGT | 84669 |
rs761322634 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon | USP32 | GRCh38.p7 | 17:60345550 | CTGGCCCATGTAATA[C/T]GAGAGTCCACAGGTC | 84669 |
rs761324016 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60222031 | TACAAGAAGAATCCA[A/C]TCCCTAACTAGATAC | 84669 |
rs761342227 | in-del | -/TTTTTTTTTTTTT | | | intron-variant, downstream-variant-500B | USP32, LOC105371850 | GRCh38.p7 | 17:60402247 | CATCCCTCATTTATC[-/TTTTTTTTTTTTT]TTTTTTTTTAATACA | 84669 |
rs761344044 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60326904 | TAAACAGTTCTCAGT[C/T]TTACGTAGATGCTAA | 84669 |
rs761357162 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60222214 | TTCAACAGCCTCCTA[-/T]TTTCCTTGCCTTTAT | 84669 |
rs761372607 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258971 | CTACTTTTTTACACA[A/G]TCCTTTAAATATATA | 84669 |
rs761374697 | in-del | -/AAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60269845 | ACTATTTTTGAAGTC[-/AAT]AAATAAAAATTAAAA | 84669 |
rs761382227 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60297911 | TAACTACAGCTTTGA[C/T]TGGACAAGAGAGCTA | 84669 |
rs761395232 | snp | A/G | 1.64825e-05 | 0.00287071 | missense | USP32 | GRCh38.p7 | 17:60192898 | TGCACAACTCGTAGA[A/G]TGAATGGATATTGAT | 84669 |
rs761395306 | snp | G/T | 1.67063e-05 | 0.00289014 | synonymous-codon | USP32 | GRCh38.p7 | 17:60209436 | ATATGGCTTTTCATG[G/T]ACTCGATTAAGATCT | 84669 |
rs761423704 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60353282 | GCAGGCCAGGAAGAG[A/G]GCCCTCACCAAAAAC | 84669 |
rs761425554 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60344285 | AGGCACCCGCCACTA[A/T]GCCCAGCTAATTTTT | 84669 |
rs761443392 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60275557 | AATGCTAACTGTGAT[A/G]AAAGATAACAATTAG | 84669 |
rs761463860 | snp | C/G/T | 4.94208e-05 | 0.00497075 | synonymous-codon, missense | USP32 | GRCh38.p7 | 17:60181498 | GTCCTGAGGAGTGAC[C/G/T]AACTCTGGTTGGCTG | 84669 |
rs761471046 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60325307 | TAATCCCAGCTACTT[A/G]GAAGGCTGAGGTGGG | 84669 |
rs761471781 | snp | C/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412592 | CATTCTGATTCTGAA[C/G]ATCTAAGGCAAGGTG | 84669 |
rs761476118 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60337568 | TTTTTTAAGTCATAA[A/C]GTCTGCCCATCAAGA | 84669 |
rs761483948 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60250536 | CTGGTTTCTACATGT[C/T]AATTATTTTAAAATC | 84669 |
rs761487138 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245103 | ATGTAATGGGAACAA[C/T]ATGGTTTTATAATTA | 84669 |
rs761497059 | in-del | -/TTTTTG | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405198 | ATAGAAGCTGTTAGT[-/TTTTTG]TTTTTGTTTTTGTTT | 84669 |
rs761501842 | snp | C/T | 5.10243e-05 | 0.0050507 | intron-variant | USP32 | GRCh38.p7 | 17:60212150 | TATCTAATTTATACC[C/T]ATTCGATTGCTTTTT | 84669 |
rs761507670 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60335356 | CTTATTCCTACACAT[-/A]AAATCTTTCTTCTAT | 84669 |
rs761514274 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60207307 | ATAAAAATAACGGAA[A/G]ACTAACCTCAATTTT | 84669 |
rs761516298 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60223284 | TGTACTATACAAAGA[C/G]ATGTCCATCTATAAT | 84669 |
rs761522850 | snp | A/G | 3.3089e-05 | 0.00406736 | intron-variant | USP32 | GRCh38.p7 | 17:60214824 | AGATGTGAAAAAGAA[A/G]CACCCCTCTCAGCAA | 84669 |
rs761526468 | snp | C/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409277 | CACTTGAACCTAGGA[C/G]GCGGAGGTTGCAGTG | 84669 |
rs761551747 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312209 | TCTCAGGACAGAAGG[C/T]GGAAACCAGAGTTTG | 84669 |
rs761563629 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60249869 | TTTTTTTTTAACAAC[A/G]TACTGACTGTAAGTT | 84669 |
rs761571202 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60285632 | GAATGCTATAAGTAG[C/T]TATAATACAAAGATG | 84669 |
rs761577288 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60259996 | TACCCTTTCACTTAA[A/G]GTTGCAGTTTCCAAG | 84669 |
rs761577420 | in-del | -/TA | | | intron-variant | USP32 | GRCh38.p7 | 17:60184651 | CATATCTACTAAAAG[-/TA]TACAAAAATTAGCCG | 84669 |
rs761600385 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60318086 | GTACAAATTGTGACA[C/T]AGAAAGCATGTGTAT | 84669 |
rs761614509 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378329 | GAAAATGGAAGGAGC[A/G]CTTGTGCATTGCTGG | 84669 |
rs761636088 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60319737 | GTGAGCCAAGATAGC[A/G]CCACTGCACTCCAGC | 84669 |
rs761650043 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60364264 | TTCCTGAAGGCCCCA[C/G]TTCTTCATACAATCA | 84669 |
rs761651563 | snp | A/G/T | 3.29458e-05 | 0.00405857 | missense | USP32 | GRCh38.p7 | 17:60183308 | AGCTCATCCCCCTGG[A/G/T]GTGTGAGTGGTTTAT | 84669 |
rs761672868 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60183940 | ATCAAACTGGATATT[-/A]AAAAATCTATGCTTT | 84669 |
rs761677631 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60272382 | CCTCAGAATATACAT[A/C]AAAAATCGCAAATAG | 84669 |
rs761770601 | snp | C/T | 1.67069e-05 | 0.00289019 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181336 | TACCGAAATTGCATA[C/T]AGATTATAAATAGGC | 84669 |
rs761791822 | snp | C/T | 0.000104455 | 0.0072261 | intron-variant | USP32 | GRCh38.p7 | 17:60208255 | AAAATGCAGGTTTCA[C/T]TGAAAGTCTTAAATG | 84669 |
rs761795412 | snp | A/G | 1.6654e-05 | 0.00288561 | synonymous-codon | USP32 | GRCh38.p7 | 17:60211393 | GTTGAGTTCATAAAG[A/G]TGTCTCCCTGAGATA | 84669 |
rs761800769 | snp | A/C | 6.62778e-05 | 0.00575626 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265460 | TACAATATCAGAGAG[A/C]TCCATATGTAATTCC | 84669 |
rs761816207 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60319651 | CAGAAGTGGTGGTGC[C/G]CACCTGTAGTCCCAA | 84669 |
rs761818092 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60361184 | AAGCTAAACATACCA[C/G]TACCATAAAATCCTA | 84669 |
rs761855692 | in-del | -/GTGGCAAC | 3.3095e-05 | 0.00406773 | intron-variant | USP32 | GRCh38.p7 | 17:60236288 | CAAAGTGTGAAATAG[-/GTGGCAAC]GCACAAAAATTATCA | 84669 |
rs761865591 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60241742 | CTTAATGTGTTGTAA[C/T]AGTCCTTTATATATT | 84669 |
rs761879410 | snp | C/G/T | 0.00030811 | 0.0124082 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231685 | CTAGCTCTAAAGTTA[C/G/T]GTGATAACTAAATAG | 84669 |
rs761883608 | snp | A/G | 5.0374e-05 | 0.00501841 | synonymous-codon | USP32 | GRCh38.p7 | 17:60208820 | TCTTCTTAGATGGTT[A/G]TCCCAGGCCTAGCAA | 84669 |
rs761891812 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60399761 | CAAAATTGGAAGGAG[A/C]GAATGAAGCAGACTT | 84669 |
rs761892554 | in-del | -/CCA | | | intron-variant | USP32 | GRCh38.p7 | 17:60245670 | AGTAGGAGATGGCTG[-/CCA]CCTCCGTAGGCAGCG | 84669 |
rs761893992 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60382919 | CAAAACTACATACTA[C/T]ATTTAGGACTATTTA | 84669 |
rs761903379 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60193463 | CCAATGATTATGTCA[A/C]GATGGCCCTGTGAAT | 84669 |
rs761912990 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393509 | TGCGTCTTCAACCTA[A/C]AAGTCACGGAATAAA | 84669 |
rs761916300 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60386328 | ACCTTAATCTTCTCA[A/G]TACACTATCCAACTA | 84669 |
rs761927937 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418116 | GGCATGTGCTACCAC[A/G]CCCAGCTAATTTTGT | 84669 |
rs761947996 | in-del | -/CCA | | | intron-variant | USP32 | GRCh38.p7 | 17:60370883 | GAGTGTCTCTTGAGG[-/CCA]CCAGGAGTTTGGGAC | 84669 |
rs761962310 | in-del | -/TAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60279853 | AATAATAATAATAAT[-/TAA]TAATAATAATAATAA | 84669 |
rs761968525 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60348653 | GTGGCACGTGCCTAT[A/G]GCTACTCAGGAGGCT | 84669 |
rs761980997 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60186641 | CTAATACTCACCCAA[A/C]CCTTTGGGGTCCTGT | 84669 |
rs761993157 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309473 | TGGGTGTGGTGGCAC[A/G]CACTTGTAATCACAG | 84669 |
rs761996740 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60329330 | AGAGGGGTCTTAGGA[C/T]AGGACTGTGTCAGAT | 84669 |
rs762057757 | snp | A/C | 1.64882e-05 | 0.00287121 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183220 | GCTTTTGCTCAGGAG[A/C]ACGTCCTCTTCCCCA | 84669 |
rs762071559 | snp | C/T | 5.37851e-05 | 0.00518553 | intron-variant | USP32 | GRCh38.p7 | 17:60211563 | TGTAGTAATATGCCA[C/T]GGCACAAACAGTTAC | 84669 |
rs762074069 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60394450 | GGAGCAAATTAATGT[A/G]TCTCTTTGTGGCACT | 84669 |
rs762075324 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60250491 | GTCACTATAGCCACA[G/T]AAAAGCCTTTATGTA | 84669 |
rs762078993 | snp | C/G | 1.74251e-05 | 0.00295165 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294841 | ATTAATCTTAACAAA[C/G]ACCAAATATACGTTG | 84669 |
rs762087138 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60297261 | AAAATTAGCTGGGCA[C/T]TGTGGTACGTGCCTC | 84669 |
rs762109678 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60304158 | AGATAAAAAGAAAAT[A/G]TTTAAGGCAGCCAGA | 84669 |
rs762120279 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60368672 | TAGTAAACATAAAGT[A/C]AGTCCAGGGGTTTAT | 84669 |
rs762127441 | snp | C/T | 3.30606e-05 | 0.00406561 | missense | USP32 | GRCh38.p7 | 17:60205506 | CAGGAAGAGATGGCA[C/T]GTGACCATTAACCAT | 84669 |
rs762131414 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227394 | CCTGCCTCAGCCTCC[C/T]GAGTAACTGGAATTA | 84669 |
rs762152475 | snp | C/T | 3.29489e-05 | 0.00405874 | synonymous-codon | USP32 | GRCh38.p7 | 17:60185547 | GTACATCTCATTTTC[C/T]CCTAGCTCTTCCTCA | 84669 |
rs762154688 | snp | A/G | 1.76328e-05 | 0.00296919 | intron-variant | USP32 | GRCh38.p7 | 17:60208019 | AAAATGTCATCTTTG[A/G]AGGATAGAATCAAAA | 84669 |
rs762155526 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60282703 | ATGAAGTTGTTAAAC[C/T]TTATTTAAACATGAT | 84669 |
rs762182394 | snp | C/G | 3.55448e-05 | 0.00421558 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231620 | TAAGGAGAACAGGGA[C/G]CCCCCAAAGCCCATG | 84669 |
rs762188832 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60361260 | CTTCCCCAAGAGATA[A/G]TCAGTTTGGTTTGTC | 84669 |
rs762199632 | snp | C/T | 1.88938e-05 | 0.00307352 | intron-variant | USP32 | GRCh38.p7 | 17:60269604 | AGCCAAGCTTCCTAA[C/T]GTTAATAATGACATG | 84669 |
rs762216513 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404384 | TTTTTTTAATGTGAT[G/T]CACATGGAAGAGGTC | 84669 |
rs762227074 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60340463 | GTTGTTGGTTTAAAG[A/T]CTGTTTTATCAGAGA | 84669 |
rs762236092 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60316143 | CATCAACCACTCTGC[C/T]ATCCATGCCAAACAT | 84669 |
rs762241894 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378883 | TCATGCCACTAATTG[C/T]ACATTTTTTAAAATA | 84669 |
rs762266028 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60267783 | CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 84669 |
rs762289592 | snp | A/G | 0.000117488 | 0.00766357 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392606 | AGGGAATGGGGTTCT[A/G]AGGGATGCGGCATAT | 84669 |
rs762310364 | snp | G/T | 1.64743e-05 | 0.00287 | missense | USP32 | GRCh38.p7 | 17:60226081 | ATGCAGTAGAAATGT[G/T]GTCTGAAAATTTCTC | 84669 |
rs762322580 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60355047 | AGGCTCTGCCTCAAA[A/G]ACAAAAACATAAAAC | 84669 |
rs762329654 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312212 | CAGGACAGAAGGCGG[A/T]AACCAGAGTTTGAAG | 84669 |
rs762331952 | in-del | -/AC | | | intron-variant | USP32 | GRCh38.p7 | 17:60386020 | CTATTGCTGCATAAC[-/AC]ACACACACACACACA | 84669 |
rs762332525 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon | USP32 | GRCh38.p7 | 17:60190593 | TTGATAGCGAAGGTG[A/G]AGGGCTGTGGGATCC | 84669 |
rs762337991 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60237398 | TGGGATTACAGACAT[A/G]AGCCACTGTGCCCAA | 84669 |
rs762380488 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60342411 | AGGAGACAGTCTGTC[C/T]GTTCTCAGAGCTCAA | 84669 |
rs762394291 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412611 | TAAGGCAAGGTGATT[C/T]TTCTGTCTGAAAAAC | 84669 |
rs762405475 | snp | A/G | 4.94401e-05 | 0.00497168 | synonymous-codon | USP32 | GRCh38.p7 | 17:60180635 | CAGAATTCCTGAATG[A/G]CACTGTAAGAGATAA | 84669 |
rs762435836 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60252171 | ATTTAGTATTCAGTG[A/C]AATTTTAATGTTAAA | 84669 |
rs762482749 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360272 | TGAGGTCAGGAGTTT[G/T]ACACCAGCCTGGCCA | 84669 |
rs762496621 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60313451 | TCCTGGAAGTAAATA[C/T]CATAAGGTAGAGTCA | 84669 |
rs762502916 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60299624 | TTAAGTTTCCACACA[A/T]GAACTTTGGGTAACG | 84669 |
rs762505665 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | USP32 | GRCh38.p7 | 17:60198345 | CCGCATCATATAGGT[C/G]TTTCTTCCGGGTATG | 84669 |
rs762529802 | snp | C/T | 1.70606e-05 | 0.00292062 | missense | USP32 | GRCh38.p7 | 17:60181643 | CCAATCTGGGGCAGC[C/T]GGAGCCTCCCTTTGC | 84669 |
rs762551650 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60287317 | CTATCTATGACCTAC[C/T]TGTAAGCTCCCCTTT | 84669 |
rs762553836 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60398348 | TACAGTTACCCATGA[A/C]TGCGTCACTGCACTC | 84669 |
rs762563066 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60337673 | CTTGAGCCTAAGAGT[C/T]TGTGACCAGCCTAGG | 84669 |
rs762573946 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60398823 | TCTCTACAAAAAAAA[A/T]AAATTTAATTAGCTG | 84669 |
rs762580340 | snp | C/G | 3.42636e-05 | 0.00413892 | intron-variant | USP32 | GRCh38.p7 | 17:60391844 | GGCTGCCCGTCGCGG[C/G]CCTCCCAGGCAGCTC | 84669 |
rs762596832 | snp | G/T | 1.76275e-05 | 0.00296874 | intron-variant | USP32 | GRCh38.p7 | 17:60219791 | GTTCTTGATAACCTA[G/T]TGTTTTAAAAGATAA | 84669 |
rs762614222 | snp | A/G | 1.66952e-05 | 0.00288917 | synonymous-codon | USP32 | GRCh38.p7 | 17:60214701 | GTGAATTTCCTTGAT[A/G]GTCTGCATTCGACTA | 84669 |
rs762619873 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60283981 | TAAAAGGGGAACAGT[-/A]AAACTCGTAAGAAAT | 84669 |
rs762621019 | snp | A/G | 3.59699e-05 | 0.00424072 | missense | USP32 | GRCh38.p7 | 17:60181739 | CTTTTTCTTGATGAA[A/G]AAGGAGAACCTGTGA | 84669 |
rs762628283 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60248202 | CTTTCTCATATCACT[C/G]CACACTGAGCTCTAT | 84669 |
rs762635621 | in-del | -/CACTTCCCTTTCTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60246672 | TCAATAGTGTACTAG[-/CACTTCCCTTTCTT]CACATCCTCATCAGA | 84669 |
rs762635910 | snp | A/T | 1.65729e-05 | 0.00287857 | synonymous-codon | USP32 | GRCh38.p7 | 17:60207040 | CTGTGTTGGACTAGA[A/T]GCTGAAATTGGAGAC | 84669 |
rs762649503 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60183736 | TTGCTCTTCTAGAGT[A/C]CACAAAGGCTTAGCC | 84669 |
rs762649958 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191091 | CTGTAAAATGGCAGA[G/T]TAAATAAATGCATAT | 84669 |
rs762656622 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60399922 | CTTTGGCTCTTGCTC[A/G]TAAAATCAGAAGCTG | 84669 |
rs762668257 | snp | A/C/T | 0.000115355 | 0.00759379 | missense | USP32 | GRCh38.p7 | 17:60345587 | AAAGCATCCTTCAGT[A/C/T]GTTTTAGCTCTACAT | 84669 |
rs762745009 | snp | C/G | 1.64955e-05 | 0.00287184 | missense | USP32 | GRCh38.p7 | 17:60209471 | GAAGACCATCCAAGA[C/G]AAAAGCCAGAAGTTC | 84669 |
rs762773736 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60184195 | TGGTGGGCGCCTGTA[C/G]TCCTAGCTACTCAGG | 84669 |
rs762781298 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60272460 | GTAAAATTTACAAAG[C/T]GTACATAGGACATTT | 84669 |
rs762785759 | snp | C/T | 3.39219e-05 | 0.00411823 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179213 | AGCTACAAGGAGTCA[C/T]CTCCCTCACCGCCAA | 84669 |
rs762799254 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60338510 | TCGAGGCAGGGTGAT[C/T]ACCTGAGCTCTGGAG | 84669 |
rs762804973 | snp | A/G | 8.70678e-05 | 0.00659745 | intron-variant | USP32 | GRCh38.p7 | 17:60208867 | TTTCTCTCAAAATCC[A/G]AAAGAGAAGCATTTC | 84669 |
rs762806266 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60240796 | CCACCACCCGCAAGA[C/T]TTTCAGCATTCTATT | 84669 |
rs762814686 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60319147 | TTTGGGATGATGAAA[A/C]GGTTTTAGAAAAAGA | 84669 |
rs762821493 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308882 | TGCAGTGAGCCGAGA[C/G]TGTGCCACTGCACTC | 84669 |
rs762823540 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60273331 | TCATACAGGGCTGGG[A/C]GATGTCTGAGTTGTG | 84669 |
rs762853173 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233359 | GAGTCTCAGCTACTC[A/G]GGAGGTGGGAGAATT | 84669 |
rs762853655 | snp | C/T | 1.66186e-05 | 0.00288254 | synonymous-codon | USP32 | GRCh38.p7 | 17:60214638 | ACTGTTGTATAGCCA[C/T]AGGCGCATATCTTCC | 84669 |
rs762855453 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405080 | TGAAGCACAAGAATT[G/T]CCTGAACCAGGGAGG | 84669 |
rs762865734 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60287063 | GCTGAGGCAGAAGAA[C/T]CGCTTGAACCTGGGA | 84669 |
rs762867766 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60320160 | AGGTTCTTGGAAACT[A/G]CAACTTCAAATGACA | 84669 |
rs762870640 | snp | A/C/G | 0.000149802 | 0.00865323 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422692 | GGTCCCGGAGGGGCT[A/C/G]GTTTTGGAAAGTAGA | 84669 |
rs762941717 | in-del | -/GAG | | | intron-variant | USP32 | GRCh38.p7 | 17:60354411 | ACAACATCTGAATCA[-/GAG]GATAACCACAGAGAT | 84669 |
rs762943381 | snp | G/T | 1.64789e-05 | 0.0028704 | synonymous-codon | USP32 | GRCh38.p7 | 17:60226175 | GGCTGCAGTTCCAAA[G/T]GAGTATTTTCCTCCA | 84669 |
rs762948613 | snp | C/T | | | upstream-variant-2KB, intron-variant, missense | USP32 | GRCh38.p7 | 17:60392351 | AACCGCGCGCAGGAG[C/T]GCCGGGGAGGGGGAC | 84669 |
rs762949960 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60329044 | GGCCCAGACAAAGGC[A/G]CCACCAGCCACACGT | 84669 |
rs762956583 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60353237 | GGAAAGAGCATGTAT[A/G]GATGCAACGAGCAGG | 84669 |
rs762978672 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366730 | ACACAGCAAGACATC[G/T]TCTCAAAAAAAAGTT | 84669 |
rs763001649 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60282983 | CAAAATCATTTCCAA[A/C]AGACTTAGAGATAGG | 84669 |
rs763015817 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60421757 | GCCCACCGCGTTTCC[A/G]CCCTCGGCCTCGGGT | 84669 |
rs763020175 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | USP32 | GRCh38.p7 | 17:60183311 | TCATCCCCCTGGGGT[A/G]TGAGTGGTTTATGCT | 84669 |
rs763020947 | snp | C/T | 1.66211e-05 | 0.00288275 | intron-variant | USP32 | GRCh38.p7 | 17:60271310 | ATGGGCTCAGGTATG[C/T]TTACCAGTGAACATA | 84669 |
rs763025104 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60316317 | GATTTTTTTTTCCCC[A/G]TGGGGTGAAAAGCTA | 84669 |
rs763031811 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60385698 | AATACAAAAATGAGC[C/T]GGGCATGGTGGTGGG | 84669 |
rs763032807 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60229451 | ATTTGTTTTTATAAT[A/G]TGCTCCAGATGTTAA | 84669 |
rs763038555 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195658 | CTCTTTTGATGCTTC[C/T]TTTTCCCTTTTCAAT | 84669 |
rs763046741 | in-del | -/CCT | | | intron-variant | USP32 | GRCh38.p7 | 17:60234651 | GAAGAATGGCGTGAA[-/CCT]CCTGGAAGGCGGAGC | 84669 |
rs763050423 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60199147 | AAAAGATGCCAGTGG[A/G]AAAAAAAAAAAAAGA | 84669 |
rs763058065 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60283929 | TAGAGCGAAGGGCTG[A/C]TCCACTGGAAATAAC | 84669 |
rs763058269 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60333982 | ATATGGGTCACATGG[C/T]GTTATTCAAGGTTTA | 84669 |
rs763060664 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60413670 | GGATATTGAGATCAT[C/T]CTGGCCAACAATAGT | 84669 |
rs763084906 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418396 | CGTGCCTGGCCTCTG[-/T]TTTTTTTTTTTTTTT | 84669 |
rs763110430 | in-del | -/GT | | | intron-variant | USP32 | GRCh38.p7 | 17:60361159 | AACAACAAAAACCCG[-/GT]GTATATATAAAGCTA | 84669 |
rs763153420 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60297400 | AACCCTGTCTCAATC[A/T]ATCAATCAATAAACT | 84669 |
rs763153581 | in-del | -/C | 3.65344e-05 | 0.00427386 | intron-variant | USP32 | GRCh38.p7 | 17:60255304 | TTTTTTTTCTTTTTT[-/C]TTTTTTTTTTTGAGA | 84669 |
rs763160136 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60361519 | TACATACAGAGAGTG[C/T]TTCTCCAGTGAGCAC | 84669 |
rs763187816 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60325533 | AACCAAAAATTGTGA[A/T]ATAATTTCACTGGAT | 84669 |
rs763203159 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230135 | TACTTTCTAAAAAAT[G/T]TGTAGTAATATATTT | 84669 |
rs763207494 | snp | C/T | 3.29457e-05 | 0.00405854 | missense | USP32 | GRCh38.p7 | 17:60205614 | GTAGGTCCCCATTGG[C/T]AGTTAGGGTGAACAT | 84669 |
rs763209308 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378994 | TGGGGGAGAGCTATG[C/T]ACATACCTGAGTTTG | 84669 |
rs763229553 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60255288 | CTCATGTTAGGAACA[A/T]CTTTTTTTTCTTTTT | 84669 |
rs763236757 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60397179 | GACTCCAACTTTGAA[C/T]ATATAGGATATACCT | 84669 |
rs763240233 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60314540 | TGAAGTACGGTGAAG[-/A]AAAAAGAGCTAGAAC | 84669 |
rs763244286 | in-del | -/AATT | | | intron-variant | USP32 | GRCh38.p7 | 17:60287150 | CAATACTTCGTCTCA[-/AATT]AATTAATTAATTAAT | 84669 |
rs763244417 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60342676 | CACCTCACAGTTTGA[C/T]CTCAGACTGCTGCGC | 84669 |
rs763251107 | snp | A/G/T | 0.000131834 | 0.00811793 | intron-variant | USP32 | GRCh38.p7 | 17:60236247 | AACCATCCTCTGTAT[A/G/T]TACAAAAGAAATTAA | 84669 |
rs763253053 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant, missense | USP32 | GRCh38.p7 | 17:60219666 | ATTCTCAGGCTCATC[A/G]TACCCATATTCACCC | 84669 |
rs763266212 | snp | C/T | 1.65231e-05 | 0.00287424 | missense | USP32 | GRCh38.p7 | 17:60183389 | CTTTCCCGAGGAAAT[C/T]TGACAATTTTCTGTG | 84669 |
rs763266953 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306200 | ATTAGCTTTCATTTT[C/T]GGATTTAGAAGACGG | 84669 |
rs763281982 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290908 | GAACTAATCCCTCAA[A/G]CTGTGGGATCTGATG | 84669 |
rs763287816 | snp | A/T | 1.64743e-05 | 0.00287 | missense | USP32 | GRCh38.p7 | 17:60190625 | AATCCACAGCGATAT[A/T]GGCATTTCCAATGAA | 84669 |
rs763294551 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60268156 | CACAACATGCTAACA[A/G]TTAGAACACCAGTGC | 84669 |
rs763300459 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194540 | TTTACTCACTAAAGA[C/T]TGCAGCACCCAGTTC | 84669 |
rs763324267 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60364016 | TTCAGGCTGCTACAA[C/T]AAAATATCTCAGATT | 84669 |
rs763330523 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60361918 | TAACACAAAGATATA[A/G]TGTTAACAGTATTAC | 84669 |
rs763337866 | snp | A/G | | | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419237 | ATGGAGCTGAAGGCC[A/G]TTATCCTTAGAAAAC | 84669 |
rs763341119 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60344665 | GTCTCACTATGCCCA[A/G]GCTGGCCTGGAACTC | 84669 |
rs763346841 | snp | C/T | 4.94482e-05 | 0.00497209 | intron-variant | USP32 | GRCh38.p7 | 17:60236128 | GTAAATAGACAGGAA[C/T]CTAACTCACGTATTT | 84669 |
rs763351749 | snp | G/T | 1.65143e-05 | 0.00287348 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271445 | GCCTTCAATAACCAA[G/T]AGCGTTTCTCAAGAT | 84669 |
rs763393825 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60278813 | GGAGAGGACTATTCA[C/T]GTACTACAGTATAGG | 84669 |
rs763403469 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60184811 | GAGACCCTGTCTCAA[-/AA]AAAAAAAAAAAAAAA | 84669 |
rs763409073 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60222181 | CCTAGGTGATGTCTA[C/T]TTTTATGTGGATAAC | 84669 |
rs763426309 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60272087 | CCCAAAGTGTTGGGA[G/T]TATAGGTGTGAGCCA | 84669 |
rs763472787 | snp | C/T | 3.29473e-05 | 0.00405864 | missense | USP32 | GRCh38.p7 | 17:60181463 | TCATAAAGGAATCCA[C/T]TGGCCAAAGCTACCT | 84669 |
rs763485021 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60292217 | TTAGTGGTCTGTTTT[G/T]AGTCCTCTTCATCTC | 84669 |
rs763496180 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60326941 | TGATCTCATAGAAGT[A/G]GAGAGTAGAATAGTG | 84669 |
rs763502495 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60371668 | AATGCAGATTAATCC[A/T]CATTGAGATACTACT | 84669 |
rs763508031 | snp | A/G | 3.31647e-05 | 0.00407201 | stop-gained | USP32 | GRCh38.p7 | 17:60211416 | CTGAGATAAAATACT[A/G]TGTCAGTGGCTGTGT | 84669 |
rs763518240 | in-del | -/T | 1.64844e-05 | 0.00287087 | intron-variant | USP32 | GRCh38.p7 | 17:60180640 | TCCTGAATGGCACTG[-/T]TAAGAGATAAGAGAG | 84669 |
rs763533698 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon | USP32 | GRCh38.p7 | 17:60190677 | AATTTTACAGCCTCT[A/G]CAAAATCTAAAAAGG | 84669 |
rs763540770 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60391073 | CCAATAAGCAGCAGG[C/G]CGGGACTGGCAGCCA | 84669 |
rs763553678 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60388974 | ATGTTTGTATGTGGT[A/G]ATATATGCCTATTTT | 84669 |
rs763553822 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60239346 | CTTTCTTTAAGTCCA[A/G]TGAGCTTTTTGAACG | 84669 |
rs763568797 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60387602 | ATACACAAGTTAGAA[C/T]TATAAACAGAATTTC | 84669 |
rs763576936 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60205677 | CAAATTCAAAGATAA[G/T]TACAGTATCATAAGC | 84669 |
rs763581882 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60199688 | AAGCTTAAATACATA[A/C]TTTTAAGCCTCTATT | 84669 |
rs763584308 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60267646 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAT | 84669 |
rs763597962 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60188842 | GCACATTCAGAAACC[A/C]TACATGTAGGGGAGC | 84669 |
rs763618652 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181417 | GTTTCCAAGCTGACC[A/G]TTGCTGTAGCCATTG | 84669 |
rs763628387 | snp | A/G | 1.73147e-05 | 0.00294228 | intron-variant | USP32 | GRCh38.p7 | 17:60208248 | TATTGGTAAAATGCA[A/G]GTTTCATTGAAAGTC | 84669 |
rs763630286 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60257746 | ACCTTGGCCTCCCAA[G/T]GTGCTGGGGTTACAC | 84669 |
rs763647690 | snp | C/T | 2.1872e-05 | 0.00330689 | intron-variant | USP32 | GRCh38.p7 | 17:60301583 | GAATTATTTTTGAGA[C/T]AATAAAAGTACTTAC | 84669 |
rs763661519 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60334582 | CTGTAGTCCCAGCTA[C/T]TTGGGAGGCTGAGGC | 84669 |
rs763662673 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60235917 | CCAATATTATCTTTT[C/T]TTAGGGTTGTTGCAA | 84669 |
rs763663202 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60275915 | ACCTTGTCTCTATTT[-/A]AAAAAAAAAAAAAAG | 84669 |
rs763680307 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290131 | TGCTCTCGAAATGTA[A/G]TTCTCTGTAAGTCCA | 84669 |
rs763706569 | snp | C/G | 3.57194e-05 | 0.00422592 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231522 | CTCAACTACACATGT[C/G]TGAGGCAGGAAAACA | 84669 |
rs763720885 | in-del | -/CTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60252057 | TAAAATCTTTCTCTG[-/CTT]CTTTTTGTTTAGCTC | 84669 |
rs763758976 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60219562 | AACGTAGTTTTCACC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTA | 84669 |
rs763763930 | snp | C/T | 1.77483e-05 | 0.0029789 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231595 | GCTGCTCTTGGCCTC[C/T]AGCCTTGGCTAAGGA | 84669 |
rs763770223 | snp | C/T | 3.29647e-05 | 0.00405971 | missense | USP32 | GRCh38.p7 | 17:60192892 | TCTTTCTGCACAACT[C/T]GTAGAGTGAATGGAT | 84669 |
rs763802987 | in-del | -/CTAGAGTCCACAAAGGCTTAGC | | | intron-variant | USP32 | GRCh38.p7 | 17:60183729 | GGCTCAGTTGCTCTT[-/CTAGAGTCCACAAAGGCTTAGC]CTAAGCTTCCACCCT | 84669 |
rs763824929 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258745 | GGACATTCCAAAATG[A/G]AATGACTCTGGAAGG | 84669 |
rs763844466 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405225 | TTTTTGTTTTTGAGA[C/T]AGAGTTTCGCTCTGT | 84669 |
rs763851834 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60373890 | AAGTTTTTACTATTC[A/G]TGTTTTATTTTCCTT | 84669 |
rs763853278 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60310092 | CAGGCAATAACAAAT[A/G]CTGGTGAGGATGTGG | 84669 |
rs763861492 | snp | A/G/T | 3.2948e-05 | 0.00405871 | missense | USP32 | GRCh38.p7 | 17:60181496 | TGGTCCTGAGGAGTG[A/G/T]CCAACTCTGGTTGGC | 84669 |
rs763883309 | snp | C/G/T | 3.62156e-05 | 0.0042552 | intron-variant | USP32 | GRCh38.p7 | 17:60223612 | AAAAGAGGATAGAAT[C/G/T]TCTTATTTTTAGTTA | 84669 |
rs763926351 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60241727 | AGATTTTCTTGATGT[C/T]TTAATGTGTTGTAAC | 84669 |
rs763939219 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60339903 | TTTTACTATTAAAAC[A/T]AAACATTATTAGCTA | 84669 |
rs763969785 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353151 | CTTATAAGGATAGGA[C/T]GCTGAACTTACAGGA | 84669 |
rs763974248 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60396449 | AATGTAAAAGATCAC[C/T]TCCAAAATATTGAAA | 84669 |
rs763974987 | snp | A/C/T | 3.29708e-05 | 0.00406011 | missense | USP32 | GRCh38.p7 | 17:60223493 | AACAAAATATTCCCA[A/C/T]TGGCTCCCAGCAAAC | 84669 |
rs763980774 | snp | A/G | 3.31137e-05 | 0.00406887 | missense | USP32 | GRCh38.p7 | 17:60301695 | TTCCACCAAAAGAAC[A/G]GTAAATCACCTGGAA | 84669 |
rs764019669 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60279655 | CAGCCCGGGCAACAT[A/G]GTAAAACCCCTTCTC | 84669 |
rs764021445 | snp | A/G | 5.01048e-05 | 0.00500499 | intron-variant | USP32 | GRCh38.p7 | 17:60209552 | TGGTCCACTATAAAT[A/G]TAAGAGAAGTCACAG | 84669 |
rs764027172 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60394804 | GCTGGAATGCAGTGG[C/T]GCAATCTCGGTTCAC | 84669 |
rs764028088 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194808 | TTACTTATTCGAACA[C/T]CCCTATTCTAATGAT | 84669 |
rs764029188 | snp | C/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60410804 | AGAAACTGTCGGCTG[C/G]GTGCGGTGGCTCACG | 84669 |
rs764049126 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60361995 | CTTCTACTATGTCCA[C/T]ACAAAGTTGTTCTTG | 84669 |
rs764051983 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232477 | TGCACCTGGCCCAAA[-/T]TTTTTTTTTTTTTTT | 84669 |
rs764061163 | snp | A/G | 1.6501e-05 | 0.00287232 | intron-variant | USP32 | GRCh38.p7 | 17:60255261 | TAAGATGACCCATCT[A/G]AAACAGAGACACTCA | 84669 |
rs764079032 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60391708 | GCCCTAATTCCCAAA[C/T]GCTGCTTCCCACCCG | 84669 |
rs764106957 | snp | C/T | 5.37447e-05 | 0.00518357 | synonymous-codon | USP32 | GRCh38.p7 | 17:60208128 | ACAGAGATCACTCAG[C/T]TGTTTTTTTAAACCT | 84669 |
rs764130661 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60255425 | GCCTCAGTCTCCCAA[A/G]TAGCTGAAATTACAG | 84669 |
rs764166369 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60316568 | GGAATGGGCCAGGCA[C/T]GGTGGCTCATGCCTG | 84669 |
rs764194474 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60255533 | TTGAACTCCTGACCT[C/T]GTGATCCATCCGCCT | 84669 |
rs764209159 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60293760 | TATACAGTCAGGAAG[A/G]CAGAGCTAACTCCCC | 84669 |
rs764245414 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60329670 | TCCTCAACTCTTAAA[A/C]GCAAAGGAGCCTTTT | 84669 |
rs764274702 | snp | C/T | 1.89439e-05 | 0.00307759 | intron-variant | USP32 | GRCh38.p7 | 17:60252372 | ATATAATTGAAACTA[C/T]AAATTTACCTAATAA | 84669 |
rs764276388 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | USP32 | GRCh38.p7 | 17:60198401 | ATTCCAAAGAGGCTG[A/G]GGCGATTCTTCTGAG | 84669 |
rs764277165 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60239709 | TTGTACATATATCAT[A/T]CTCTTGGTTTCATTT | 84669 |
rs764284173 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60313917 | TAGATACAAGAAACA[G/T]AAAATTGTAACCAAT | 84669 |
rs764294511 | in-del | -/T | 1.82058e-05 | 0.00301705 | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60231694 | AAGTTACGTGATAAC[-/T]AAATAGGAAAATCTG | 84669 |
rs764353408 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416514 | AAAAAAATGTGGTGG[A/G]GGGATGACTTTGTTG | 84669 |
rs764361669 | snp | C/G | 1.65509e-05 | 0.00287666 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269468 | TTTGTCTTTCAGCCA[C/G]GGGTCCCCTGCAACA | 84669 |
rs764362712 | snp | A/G | 1.65021e-05 | 0.00287241 | intron-variant | USP32 | GRCh38.p7 | 17:60236274 | TTAAATACATCAAAC[A/G]AAGTGTGAAATAGGT | 84669 |
rs764363973 | snp | C/T | 3.60555e-05 | 0.00424576 | intron-variant | USP32 | GRCh38.p7 | 17:60183119 | GAAACATATGTAGCC[C/T]ACAGGAGTCCCAAGA | 84669 |
rs764365957 | snp | A/G | 3.33317e-05 | 0.00408224 | intron-variant | USP32 | GRCh38.p7 | 17:60205404 | ACTATTTCACAAATG[A/G]CACTAGCAAGACTGG | 84669 |
rs764393851 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60289079 | GTGGCGCGATCTCGG[C/G]TCACTGCAAGCTCTG | 84669 |
rs764400725 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60248604 | TTCTGTTTTGCTGAA[C/T]ATTTCTCTGTCAACT | 84669 |
rs764403289 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60280959 | TAGTAAGACTCACTA[A/C]GAAAGTAGCTGCTTG | 84669 |
rs764453930 | in-del | -/TT | | | intron-variant | USP32 | GRCh38.p7 | 17:60224969 | GAGGCATCTGAATTC[-/TT]TCTCAGTATTTTAAC | 84669 |
rs764454603 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, intron-variant | USP32 | GRCh38.p7 | 17:60288607 | CACCTCCAGATAGAA[A/G]CCATCGAGAGAAAGT | 84669 |
rs764466068 | snp | C/G | 3.3264e-05 | 0.0040781 | missense | USP32 | GRCh38.p7 | 17:60207035 | CCTGTCTGTGTTGGA[C/G]TAGAAGCTGAAATTG | 84669 |
rs764479839 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | USP32 | GRCh38.p7 | 17:60185529 | CTTACACTTGGAACA[A/G]TAGTACATCTCATTT | 84669 |
rs764510986 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60324188 | TTGGGAGGCTAAAGC[A/G]GGAAGATTGGTTGAA | 84669 |
rs764516356 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403003 | GCTGGTGTAGTGGGC[A/G]GGTAAGCCGTATCTC | 84669 |
rs764520079 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60193504 | TTAAAAAAATTTACT[C/G]ATCCTTGCCCTAACA | 84669 |
rs764529529 | snp | C/G | 3.38644e-05 | 0.00411474 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391958 | CCCCTCATCCCCTCG[C/G]CGGGGGGTCGGAGCC | 84669 |
rs764539626 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60386282 | AGAAGCCATGCTTCC[C/T]GGATACAGTATAAAA | 84669 |
rs764542663 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60234724 | GACAAAAGCAAGACT[C/T]CGTCTCAGAAAAAAA | 84669 |
rs764551930 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393314 | ACCTCTCCATTTCCC[-/A]AAGAATGAAAAGCAG | 84669 |
rs764555080 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60301470 | TTGCACATTTTTTAG[G/T]TGTTTATTTACCACT | 84669 |
rs764563697 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60302551 | TACAATGGGTTTATC[A/G]GGCTGTAATCCCAGG | 84669 |
rs764565798 | in-del | -/TG | | | intron-variant | USP32 | GRCh38.p7 | 17:60301166 | CTGTACAAGTTTTTT[-/TG]TGTGTGTGTGTGGTA | 84669 |
rs764569932 | snp | C/T | 1.66751e-05 | 0.00288744 | intron-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179470 | AAAAAGCCATCACTA[C/T]TATGGCTCTAAATCC | 84669 |
rs764606054 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, utr-variant-5-prime, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266064 | GAGAGAACTCCATCA[C/T]GGTCAACATCAAATA | 84669 |
rs764612060 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60192020 | TAACGAGAGGCTTGG[C/T]GTGGTGGCTCACACC | 84669 |
rs764617478 | snp | C/T | 5.08574e-05 | 0.00504243 | intron-variant | USP32 | GRCh38.p7 | 17:60391867 | GGCAGCTCGCCCAGA[C/T]CCCTCCCCCCTCACC | 84669 |
rs764638281 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60340370 | ATCATTTGAGCTCAG[A/G]AGTTCAAAACCAGCC | 84669 |
rs764687375 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60267661 | GAGTAGCTGGGACTA[C/T]AGGTGTCCACCACCA | 84669 |
rs764694777 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60189012 | CCTAAAGAGCTTTTC[C/T]GATTGCACACTGGAT | 84669 |
rs764698272 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60259073 | AGGTATTTTCCACAT[A/G]TTGGCCCAGCTAAAA | 84669 |
rs764698884 | in-del | -/TAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60180870 | AATTGTAATTACTAT[-/TAT]TATTATTATTATTAT | 84669 |
rs764702784 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60351517 | CACTGCAACCTCTGT[C/G]TCCCGGGTTCAAGCA | 84669 |
rs764719694 | in-del | -/TTCATGCAGTTATTC | | | intron-variant | USP32 | GRCh38.p7 | 17:60250227 | ATGAGAGACACTAAT[-/TTCATGCAGTTATTC]TTCATGCAGTTATTC | 84669 |
rs764751682 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60246086 | TATTTTTAACTATAG[A/T]TACCCTACTGTGCTA | 84669 |
rs764760841 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60260302 | GAGGCAGGTGGATCA[C/T]CTGAGGTCAGGAGTT | 84669 |
rs764763177 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60359670 | AAAAATATTAGCATG[C/G]TGGTGTGCACCTGTA | 84669 |
rs764782878 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60371452 | CACGCCTATATAATC[C/T]CAGCTACTCAGGAAG | 84669 |
rs764789954 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60331103 | CAACCAAAATACAAA[C/T]GCCCTAACAAAGATA | 84669 |
rs764790820 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60411094 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 84669 |
rs764796109 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60243697 | TTGTACAGAATCAGG[C/T]AGTGGGACAAAGTTG | 84669 |
rs764800762 | snp | C/T | 3.62138e-05 | 0.00425507 | intron-variant | USP32 | GRCh38.p7 | 17:60255306 | TTTTTTTCTTTTTTT[C/T]TTTTTTTTTGAGACG | 84669 |
rs764804692 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412608 | ATCTAAGGCAAGGTG[A/C]TTTTTCTGTCTGAAA | 84669 |
rs764856540 | snp | C/G | 1.88553e-05 | 0.00307039 | intron-variant | USP32 | GRCh38.p7 | 17:60213541 | TCTTTAAATTCTTCC[C/G]CTTGAAAATTTAATA | 84669 |
rs764860751 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60281744 | GTAGTCTGTGTGACA[C/T]AGAGGTTGAAGAACT | 84669 |
rs764890697 | snp | C/G | 3.35604e-05 | 0.00409623 | intron-variant | USP32 | GRCh38.p7 | 17:60301729 | GATGATAAAGCCAAC[C/G]TTAGGAGGCATTTCA | 84669 |
rs764921114 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60196021 | TCACGCCTGTAATCC[C/T]ACCACTTTGGGAGGC | 84669 |
rs764934740 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60398220 | AATAAAAATTAAATT[A/G]CTAGCCATCTCAAAA | 84669 |
rs764940536 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60271131 | ATACATGAGCATGCT[C/T]GGGTGCAGAGAGCTA | 84669 |
rs764947108 | snp | C/T | 5.03512e-05 | 0.00501728 | missense | USP32 | GRCh38.p7 | 17:60181625 | GACAGTTTATTTTTG[C/T]TGCCAATCTGGGGCA | 84669 |
rs764970121 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60318222 | TTAATCTATTTAAAC[G/T]GCAGTTTCCTTATAA | 84669 |
rs764972058 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404593 | ACTTTTCAATTATCT[C/T]TGTATGACCTACTAC | 84669 |
rs764973131 | snp | A/G | 1.75286e-05 | 0.00296041 | intron-variant | USP32 | GRCh38.p7 | 17:60208261 | CAGGTTTCATTGAAA[A/G]TCTTAAATGCTGTGT | 84669 |
rs764982677 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60315452 | AAATAACAAGAATGT[-/A]AAAAAAACCCCTGCA | 84669 |
rs764990037 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60396840 | TTGTGTGAATTAAAG[C/T]TTACCCTATGTTATA | 84669 |
rs764995492 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60297968 | GTCTCCTGATAAGAA[A/G]ACCACTGACCATGGA | 84669 |
rs765039800 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60337585 | TCTGCCCATCAAGAA[C/T]AACAATTTTGGCTGG | 84669 |
rs765046435 | snp | A/G | 4.94295e-05 | 0.00497115 | synonymous-codon | USP32 | GRCh38.p7 | 17:60226070 | TGAGGCTTCAGATGC[A/G]GTAGAAATGTTGTCT | 84669 |
rs765094485 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60382974 | AAGCACAGGCCGGGC[A/G]CGGTGGTTCACTCCT | 84669 |
rs765110815 | snp | C/T | 3.31625e-05 | 0.00407188 | synonymous-codon, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271480 | GATGTCTGATTCCTC[C/T]ACTAAGGGTCAAATC | 84669 |
rs765118704 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60260518 | CAAGAGCAAGACTTT[-/A]AAAAAAAAAAAAAAA | 84669 |
rs765125393 | in-del | -/AGGC | 0.000132089 | 0.00812572 | intron-variant | USP32 | GRCh38.p7 | 17:60214805 | TCACAGTAAGAAAAA[-/AGGC]AGATGTGAAAAAGAA | 84669 |
rs765137656 | in-del | -/TTATA | | | intron-variant | USP32 | GRCh38.p7 | 17:60354194 | CTATTATATACTGCT[-/TTATA]TTATAACTTTTTTTC | 84669 |
rs765154982 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60344983 | TATTATTTTTAGAAA[A/C]AGAATATATCAACTT | 84669 |
rs765161453 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182376 | TCACTGTCAAAGTGA[C/T]GATATTATTCCATGT | 84669 |
rs765190818 | snp | A/G | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423326 | GCCTCCTGAGTAGAT[A/G]GGATTACAGGTATGC | 84669 |
rs765194436 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60230714 | GTCAGCACAACTCAG[C/G]TTCCTTCTTCCCCTT | 84669 |
rs765199917 | snp | C/G | 1.69012e-05 | 0.00290694 | synonymous-codon | USP32 | GRCh38.p7 | 17:60208826 | TAGATGGTTGTCCCA[C/G]GCCTAGCAATAAAAA | 84669 |
rs765205617 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227692 | GGCTAGGATTAAAGG[C/T]GTGAGCCACTGTGCC | 84669 |
rs765209432 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60223617 | AGGATAGAATCTCTT[A/C]TTTTTAGTTATTATA | 84669 |
rs765212072 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60307670 | GGCAGGGAAGTGCTG[G/T]GTAGAGAAAGGCAGG | 84669 |
rs765222192 | snp | A/G | 1.69542e-05 | 0.0029115 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391961 | CTCATCCCCTCGGCG[A/G]GGGGTCGGAGCCTGA | 84669 |
rs765233477 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60218755 | ATTACAGCACCACCA[C/T]GCCCAGCTAATTTTT | 84669 |
rs765245739 | snp | C/T | 1.65181e-05 | 0.00287381 | intron-variant | USP32 | GRCh38.p7 | 17:60190702 | AAAAGGGGGAAAAGA[C/T]CCACAGAGGAAGAAA | 84669 |
rs765248219 | in-del | -/T | 0.000141794 | 0.00841883 | intron-variant | USP32 | GRCh38.p7 | 17:60249699 | ACCAAGGATTAGTAG[-/T]TCTTGAATAAATGCT | 84669 |
rs765248959 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60197371 | GCACTTTGGGAGGCT[A/G]AGGCAGGTGGATCAC | 84669 |
rs765249922 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60184187 | AGGCGTGGTGGTGGG[C/T]GCCTGTAGTCCTAGC | 84669 |
rs765254615 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295837 | ATGTATAGGAAGAAA[C/T]GGTATATATAGGGTT | 84669 |
rs765254859 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60330058 | CCACTCACTAGCTTC[C/T]TTTAAAGCAATATTT | 84669 |
rs765261569 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60319879 | AAATAATCTAGAGAT[A/G]ATTTAAAGTATACGG | 84669 |
rs765270466 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60374580 | TTGTAGAGACAGGTT[G/T]TCACCATGTTGCCCA | 84669 |
rs765275577 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60364289 | CAATCACATTGGGAA[C/T]TAGGTTTCAACATAT | 84669 |
rs765293768 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378793 | AAAAAAAGGGATAGA[A/G]AATTTCTGTTTGGGA | 84669 |
rs765295042 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60394521 | GCTTTCATGAGATGG[C/T]AAATGATTTACAAAA | 84669 |
rs765309148 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306415 | AGCCGAGGGGGGTGG[A/C]TCATTTGAGGTCAGG | 84669 |
rs765324553 | in-del | -/CTTT | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406816 | CTGCGCCTGGCCTTT[-/CTTT]CTTTCTTTCTTTCTT | 84669 |
rs765333381 | snp | C/T | 1.64939e-05 | 0.0028717 | missense | USP32 | GRCh38.p7 | 17:60192916 | AATGGATATTGATAG[C/T]CCATACTGTCGTCAC | 84669 |
rs765339438 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60264556 | AACAAAAGAAATTTC[C/T]TGAAAGAATAGATGT | 84669 |
rs765343477 | snp | C/G | 1.66496e-05 | 0.00288522 | synonymous-codon | USP32 | GRCh38.p7 | 17:60211399 | TTCATAAAGATGTCT[C/G]CCTGAGATAAAATAC | 84669 |
rs765360936 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60248970 | GTGTGTTTTGTTTTG[C/T]TTTACGACTTCCTGG | 84669 |
rs765363260 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195993 | AAAGCCGGCCTGGGC[C/T]GGGTGCAGCAGCTCA | 84669 |
rs765364753 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60241848 | TCTTAATGCTCTCTC[C/T]TGAAACTCAAACGTT | 84669 |
rs765381930 | snp | C/T | 1.67677e-05 | 0.00289544 | intron-variant | USP32 | GRCh38.p7 | 17:60205420 | CACTAGCAAGACTGG[C/T]AGTGAGTTGCCTAAC | 84669 |
rs765409399 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60193751 | GAAGGTAATGAAACC[A/G]TGATAAAGAGTCACT | 84669 |
rs765418831 | snp | C/T | 1.64876e-05 | 0.00287116 | missense | USP32 | GRCh38.p7 | 17:60223470 | CTGGTTTCTGAGGGT[C/T]AAGGTGCAACAAAAT | 84669 |
rs765421340 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60315172 | GGAGGCCGAGGTGGG[C/T]GGAATGCCTGAGCTC | 84669 |
rs765428883 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60281293 | CCTGTAATCCCAGCA[A/C]TTCGGGAGGCCGAGG | 84669 |
rs765453908 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295003 | ACATGCCAAATTTGC[-/A]AAAAATCTTTAGGTA | 84669 |
rs765458415 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377703 | CAAGCAGCACTGTTA[A/C]AGATATCATTTCCTC | 84669 |
rs765480811 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265004 | TATTCCAACTTCTAT[C/T]ACTATTTGTTAGTTT | 84669 |
rs765508493 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60320549 | GTTGGGATGAGGGAA[A/G]AAACCGGGGTACCTG | 84669 |
rs765515873 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60222575 | ATAGAATGACAATGT[C/T]GACTTTCAATATTAC | 84669 |
rs765526479 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60290202 | CATCGCCCACCAACT[G/T]AAGTTTGCCAGCTCC | 84669 |
rs765584467 | snp | A/G | 3.29826e-05 | 0.00406082 | intron-variant | USP32 | GRCh38.p7 | 17:60236261 | TGTACAAAAGAAATT[A/G]AATACATCAAACAAA | 84669 |
rs765589267 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416810 | CAGCTAAGCTTTGAG[A/G]TACTAACAGTTATTT | 84669 |
rs765595386 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60204079 | TTTTTCTTTTTTACC[-/AA]AGAGTCAACCTTTAA | 84669 |
rs765602324 | snp | C/T | 1.70026e-05 | 0.00291565 | intron-variant | USP32 | GRCh38.p7 | 17:60185684 | AGGAGGAAAGGGGTG[C/T]GTGGGAAGGCATTTA | 84669 |
rs765622175 | snp | A/G | 1.64874e-05 | 0.00287113 | intron-variant | USP32 | GRCh38.p7 | 17:60180643 | CTGAATGGCACTGTA[A/G]GAGATAAGAGAGTGG | 84669 |
rs765643000 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60227142 | CATATTTTCTCTATT[G/T]CTCTTTTTAACAAAG | 84669 |
rs765648364 | snp | C/T | 1.65542e-05 | 0.00287695 | intron-variant | USP32 | GRCh38.p7 | 17:60180497 | AATGTTCCCCAGTTC[C/T]GTTGATATTCTGTTT | 84669 |
rs765656958 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60275566 | TGTGATAAAAGATAA[A/C]AATTAGTACCAGACA | 84669 |
rs765657592 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60397055 | TTCCCATGTGGCAGC[C/T]GGACTGTACATTTAG | 84669 |
rs765677367 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60303255 | AACTAGAAGAAAATA[A/G]CAGGGAAAAACAAAA | 84669 |
rs765683008 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60401998 | TAGCCTCATGGGCAA[C/G]CTTTCTGGAAAAGGG | 84669 |
rs765685956 | snp | C/T | 1.77669e-05 | 0.00298046 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231549 | AACAAGGCTGCCCCA[C/T]TCGTGGCAGTCCTGA | 84669 |
rs765694275 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60369700 | AATACTTGCAGCAAA[A/T]TAGTGAAATAGTTGA | 84669 |
rs765699335 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60358829 | CTGACAACTAAGAAA[A/G]TATAGCTTAGTCTAT | 84669 |
rs765726392 | in-del | -/TG | | | intron-variant | USP32 | GRCh38.p7 | 17:60387965 | ATCGTAAAGTTAAAT[-/TG]TAAGTCGGGGATTGT | 84669 |
rs765730734 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60342437 | CTCAAATGCCATGCC[A/G]GGAGAGCCACTGCTC | 84669 |
rs765736234 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388850 | CTTCTAAAATGTAAC[C/T]GAAGTCACTAGACTG | 84669 |
rs765776058 | snp | A/G | 8.26453e-05 | 0.00642774 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269491 | CTGCAACAGGCTGAT[A/G]ACCCACAGGATATCT | 84669 |
rs765784817 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60325403 | AGCCTGGGTGACAGC[A/G]CAAGACCCTGTCTCA | 84669 |
rs765849277 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60245360 | CTGCTCTTTCCACAA[C/T]GTCTTTGCAGTTCTT | 84669 |
rs765853702 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60335298 | TTGCCTGAGTCCCTG[A/C]AAATATTAAGTATGT | 84669 |
rs765857818 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414783 | AGTTGCTCATTTACT[C/T]CTCCAGGCTAGCTAG | 84669 |
rs765859091 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60281405 | TAGCCAGGCGCGGTA[A/G]CAGGCGCCTGTAATC | 84669 |
rs765893647 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60355157 | TGATGCTCACAGATA[C/T]TATACTAAGTAAAAG | 84669 |
rs765898199 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60385011 | AGCCATCACATCCCC[G/T]GTGACCTGCACAATA | 84669 |
rs765910049 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60398356 | CCCATGACTGCGTCA[C/G]TGCACTCAAGCCTGG | 84669 |
rs765917563 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60262250 | AGGCTGGAGTGCAAT[A/G]GTGTCATCTTGGCTC | 84669 |
rs765925689 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412766 | AGATGCATTTTTTTC[C/T]TCTCCAAAATCATTC | 84669 |
rs765929495 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60301237 | GGAATTGCTGGGACA[C/T]ACAGTAACAACGTTT | 84669 |
rs765950688 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60400013 | TCTGTTGTTGACCCT[A/G]GAGTGCAGTAGTGTG | 84669 |
rs765960768 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393678 | AAGAAGGTAATATTC[-/TG]TGTTTTTCTTTTTTT | 84669 |
rs765962415 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60338663 | TGACTTCAGGAGGTC[A/G]AGGATGCAGTGAGCC | 84669 |
rs765988392 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266027 | TAAAAGTGCAACCAC[C/T]ATGTCTCTCAGTTCA | 84669 |
rs765998835 | snp | A/G | 1.81529e-05 | 0.00301266 | missense | USP32 | GRCh38.p7 | 17:60181743 | TTCTTGATGAAGAAG[A/G]AGAACCTGTGAACAG | 84669 |
rs766024811 | snp | A/G | 1.7433e-05 | 0.00295232 | intron-variant | USP32 | GRCh38.p7 | 17:60208868 | TTCTCTCAAAATCCA[A/G]AAGAGAAGCATTTCT | 84669 |
rs766077403 | snp | A/G | 1.6743e-05 | 0.0028933 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265490 | CTTTAAAAATAACCC[A/G]AAGGAGTAATTAGAA | 84669 |
rs766098278 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60218132 | AAACACTACTGAAAG[A/G]ATTCTTACCAAACAG | 84669 |
rs766112802 | snp | A/G | 3.33023e-05 | 0.00408044 | intron-variant | USP32 | GRCh38.p7 | 17:60192948 | GAAACAGAAGAGAAC[A/G]AAAAGAGTGTAAGAA | 84669 |
rs766131041 | snp | C/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60423532 | GCAGTGGCTCAGTCT[C/T]GGCTCACTGCAACCT | 84669 |
rs766137278 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60283673 | AAGAACAAGTTTGCC[-/T]TTTTTTTTTTTTAAT | 84669 |
rs766154070 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60209099 | TACTTTAGCAATTAC[A/G]GGGACTCTTTAAATT | 84669 |
rs766163317 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60401497 | GGGGCTATCAATGTG[C/T]AATACTTGACAGGAA | 84669 |
rs766172179 | snp | C/T | 1.77631e-05 | 0.00298014 | missense, intron-variant | USP32 | GRCh38.p7 | 17:60288681 | TAGTTTACCTTTTCA[C/T]CCTAAAATTAAAACA | 84669 |
rs766178489 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60215425 | TCTGGCTGCACTCAG[C/T]TGAGTCACAGTCAAT | 84669 |
rs766178639 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60237441 | TATTTTTTTGAGGTG[-/A]AAATGGCATAATATG | 84669 |
rs766193854 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60321346 | GGAACTACAACCAAC[A/G]TAAGACTGGTGGGAA | 84669 |
rs766194250 | snp | A/G | 6.64485e-05 | 0.00576366 | missense | USP32 | GRCh38.p7 | 17:60214643 | TGTATAGCCACAGGC[A/G]CATATCTTCCTCTTT | 84669 |
rs766222222 | snp | C/G | 1.64885e-05 | 0.00287123 | missense | USP32 | GRCh38.p7 | 17:60209477 | CATCCAAGAGAAAAG[C/G]CAGAAGTTCTTGGGA | 84669 |
rs766257281 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393566 | AAAAGTAACCATTTG[G/T]ATTAGATTGGACCCA | 84669 |
rs766284234 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60292736 | CTCAATTGGACTCAG[G/T]TCAGCCTACTTCCCA | 84669 |
rs766284357 | snp | C/T | 1.64844e-05 | 0.00287087 | missense | USP32 | GRCh38.p7 | 17:60226182 | GTTCCAAATGAGTAT[C/T]TTCCTCCATTCAAAA | 84669 |
rs766303446 | in-del | -/CT | | | intron-variant | USP32 | GRCh38.p7 | 17:60233982 | TGAGACAGGGTCTTG[-/CT]CTGTCACCCAAACTG | 84669 |
rs766308690 | snp | C/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32, LOC105371850 | GRCh38.p7 | 17:60419241 | AGCTGAAGGCCATTA[C/T]CCTTAGAAAACTAAC | 84669 |
rs766309704 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60294155 | AAGAGATCTTCTCAC[C/G]TGGGTCACCCAAAGT | 84669 |
rs766311900 | snp | A/G | 1.65064e-05 | 0.00287279 | synonymous-codon | USP32 | GRCh38.p7 | 17:60198271 | TCACCAATCCTGGGC[A/G]TGATTACTAGCTTCC | 84669 |
rs766320498 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60257225 | TTTTATTAAAAAAGC[C/T]TTATAGGGTGGATTC | 84669 |
rs766329419 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60268298 | GCAGAGCTGGGCATG[C/G]AGGCTCATGTCTATA | 84669 |
rs766334182 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60197950 | TATACAAATTTCCTG[G/T]TGAATTCATACTCTC | 84669 |
rs766346798 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407409 | AAATAACTTAGTGAC[C/T]TCCCAAGATGTTCAG | 84669 |
rs766356995 | in-del | -/T/TCTTTTTTT | 0.000174937 | 0.00935092 | intron-variant | USP32 | GRCh38.p7 | 17:60255287 | CTCATGTTAGGAACA[-/T/TCTTTTTTT]TCTTTTTTTTCTTTT | 84669 |
rs766361934 | snp | A/G | 1.65781e-05 | 0.00287902 | intron-variant | USP32 | GRCh38.p7 | 17:60271323 | TGTTTACCAGTGAAC[A/G]TATGTAGAAAATGGA | 84669 |
rs766384194 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60225828 | GCGTGGTGGCGGGTG[C/T]CTGTAATCGCAGCTA | 84669 |
rs766389546 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60308906 | TGCACTCTAGCCTGG[C/T]GACAGAGCAAGACTC | 84669 |
rs766389706 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60398437 | GTTTTGGCAACCCTG[-/T]TTAGTCACTGGTGTT | 84669 |
rs766395923 | snp | C/G/T | 0.000345602 | 0.0131408 | intron-variant | USP32 | GRCh38.p7 | 17:60213576 | TGCATGCTTCCATCT[C/G/T]GTACCTTCAATTACC | 84669 |
rs766399049 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60316383 | CGGAAATCAGGTATA[A/G]GGAGTTTTTCTATTT | 84669 |
rs766412560 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60379239 | TTTTACAGCAATGCA[A/G]ATGTCAAAGTAGCAC | 84669 |
rs766420364 | in-del | -/CT | | | intron-variant | USP32 | GRCh38.p7 | 17:60188541 | AAATGTTAGCAAAAA[-/CT]CCTGGTAATCATTTT | 84669 |
rs766426907 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194594 | CTCCTGTTATTATTC[C/T]TGGTGACATCAACAT | 84669 |
rs766457688 | in-del | -/TTTGTTTATTTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60302109 | TATATAAATATTTTG[-/TTTGTTTATTTA]TTTGTTTATTTATTT | 84669 |
rs766475170 | snp | A/T | 1.73435e-05 | 0.00294473 | intron-variant | USP32 | GRCh38.p7 | 17:60223599 | AGCCTATAAAAAAAA[A/T]AGAGGATAGAATCTC | 84669 |
rs766484218 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60346828 | GCTGGTCAGAAATTA[C/T]AGTTTGCTTCAAAGT | 84669 |
rs766484275 | snp | A/G | 1.70691e-05 | 0.00292134 | missense | USP32 | GRCh38.p7 | 17:60181644 | CAATCTGGGGCAGCC[A/G]GAGCCTCCCTTTGCT | 84669 |
rs766496009 | snp | A/C/G | 9.88377e-05 | 0.00702923 | missense | USP32 | GRCh38.p7 | 17:60183325 | TGTGAGTGGTTTATG[A/C/G]TGGCAGAGAGCCGGG | 84669 |
rs766501052 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60193914 | TCAAAAGAAAGATAA[C/T]GGGATAAAACAGTCA | 84669 |
rs766503019 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60229528 | CTTGTGTTTTAGAAG[A/T]AGATTTAGATTTATT | 84669 |
rs766558212 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290400 | ATGTTGCAGGGACAT[A/G]TGAGTACACTGCCAA | 84669 |
rs766567474 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179052 | TGAAAGTTCTCTATC[A/G]GAGAGCTTGTATGAG | 84669 |
rs766602825 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60319834 | CTATAACAACTATTC[A/C]CGTAGTATTTACATT | 84669 |
rs766619860 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60195692 | TAAATGTCGGAATGC[A/G]TATGAACTCAGTTCA | 84669 |
rs766651288 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60421910 | TGTGTGAAGCGGGAC[C/G]GCTGCGGTACCTGCC | 84669 |
rs766676328 | snp | C/T | 6.60928e-05 | 0.00574822 | missense | USP32 | GRCh38.p7 | 17:60183390 | TTTCCCGAGGAAATT[C/T]GACAATTTTCTGTGA | 84669 |
rs766710912 | in-del | -/TTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60302110 | TATATAAATATTTTG[-/TTT]GTTTATTTATTTATT | 84669 |
rs766723464 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60252514 | TGCATGAGACCCATT[C/T]CCTAAATTGGAATCT | 84669 |
rs766724671 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60333477 | TGGTGGCATGCTCCT[C/G]TAGTCCCAGCTACTT | 84669 |
rs766736472 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60190338 | ACGTACTCTGTTATA[G/T]CAACACAAAATGGAC | 84669 |
rs766737458 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403206 | TAGTAGAGACAGGGA[C/T]AGGGTTTCACCATGT | 84669 |
rs766740427 | snp | C/T | 1.64743e-05 | 0.00287 | missense | USP32 | GRCh38.p7 | 17:60219673 | GGCTCATCATACCCA[C/T]ATTCACCCAGATGTT | 84669 |
rs766754497 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60290963 | CACCTTCATACAGAG[C/T]TAATACCAAATGTTT | 84669 |
rs766775037 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60259937 | AGAAATATGCTGTAG[G/T]AACTTAACTCTTGTT | 84669 |
rs766778526 | in-del | -/AG | | | intron-variant | USP32 | GRCh38.p7 | 17:60294060 | ATTATTTTTGAAAAC[-/AG]AAAAAATGACTTTCC | 84669 |
rs766796009 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60241066 | GCAGTGGCTCAATCT[C/T]AGCTCACTGTAACCT | 84669 |
rs766797074 | snp | C/T | | | missense | USP32 | GRCh38.p7 | 17:60198263 | CCCTGAACTCACCAA[C/T]CCTGGGCATGATTAC | 84669 |
rs766808194 | in-del | -/GAG | | | intron-variant | USP32 | GRCh38.p7 | 17:60329372 | AGAATTGTTGACTAT[-/GAG]TATATGCTAGGTATG | 84669 |
rs766814768 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60302741 | GAAAACTTACGCACA[A/T]TACTTTGATTGGAAA | 84669 |
rs766828112 | snp | C/T | 1.64781e-05 | 0.00287033 | splice-donor-variant | USP32 | GRCh38.p7 | 17:60236137 | CAGGAATCTAACTCA[C/T]GTATTTGACATATTC | 84669 |
rs766829124 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60389860 | TCTCTACTAAAAATA[-/C]AAAAAAATTAGCCGG | 84669 |
rs766834576 | snp | A/G | 1.65138e-05 | 0.00287343 | intron-variant | USP32 | GRCh38.p7 | 17:60345431 | TCAGGAATTTAGGCT[A/G]GTGGAGGTGGATAAC | 84669 |
rs766845183 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60389077 | TCTGTAGTTTTGTCA[A/C]GCTTGTTTTGCACAC | 84669 |
rs766867900 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60373073 | TCTATAGGCTAAGGT[A/G]GGAGGATAGCTAGAG | 84669 |
rs766884024 | snp | G/T | 9.94382e-05 | 0.00705048 | synonymous-codon | USP32 | GRCh38.p7 | 17:60211429 | CTGTGTCAGTGGCTG[G/T]GTGTTACTAACACAC | 84669 |
rs766896176 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404952 | GAGGCCGAGGCAGGC[A/G]GATCTCTTGAGGTGA | 84669 |
rs766906136 | in-del | -/AC | | | intron-variant | USP32 | GRCh38.p7 | 17:60388293 | AGCCGATTCTTACAC[-/AC]ACACACACACACACA | 84669 |
rs766937352 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60189287 | GAGCCTTGGTGTGTG[C/T]GGCATATTTTGGGAT | 84669 |
rs766958064 | snp | C/T | 9.9108e-05 | 0.00703876 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271448 | TTCAATAACCAATAG[C/T]GTTTCTCAAGATCAA | 84669 |
rs766962755 | snp | G/T | 1.78745e-05 | 0.00298947 | missense | USP32 | GRCh38.p7 | 17:60208075 | TTTATGTTGGAACCA[G/T]GTACTTCTGCTAGAA | 84669 |
rs766962890 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60388387 | CAGATAAGACAGAAG[-/AA]AATTAAAAAACTGGT | 84669 |
rs766973616 | snp | C/T | 1.67953e-05 | 0.00289782 | missense | USP32 | GRCh38.p7 | 17:60205454 | TAACTAACCATTTTT[C/T]GGTGGACTGCAATGA | 84669 |
rs766990376 | snp | C/G/T | 3.32271e-05 | 0.00407586 | synonymous-codon, missense | USP32 | GRCh38.p7 | 17:60207082 | AATTTCAAATGCACA[C/G/T]AAAAATCCACTCACT | 84669 |
rs767000506 | in-del | -/AG | 3.2981e-05 | 0.00406071 | intron-variant | USP32 | GRCh38.p7 | 17:60180649 | GCACTGTAAGAGATA[-/AG]AGAGAGTGGAGGTAT | 84669 |
rs767001565 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60232335 | ACGCCACCACGCCAG[A/G]CTAATTTTTATATTT | 84669 |
rs767004963 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60233938 | TTTATTGTAACTCTA[A/C]GTTTGCCTTTATTTA | 84669 |
rs767035078 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60311589 | ACACTTTGGGAGGCC[G/T]AGGATGGTGGATCAC | 84669 |
rs767045969 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60385142 | CCCACCTTAACTGAG[C/G]GATTAACTTTGTGAA | 84669 |
rs767054763 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60248327 | AGTTTTCAACACTTT[A/G]ACAATGATATGTCTA | 84669 |
rs767062719 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60323512 | AAGTAAGGTTTCTTT[C/T]TGGGGAGATGAAACT | 84669 |
rs767074426 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60338740 | GTCTCAAAAAAAACA[C/T]AGTGGCCTTGGTTCA | 84669 |
rs767080277 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60230621 | ACAAACTAGACTGGT[-/C]CTGTCTTCTCATTGT | 84669 |
rs767085209 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60385988 | GATACATCTCTGACT[A/G]TAAAAGAAAATTCTA | 84669 |
rs767088801 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60187664 | CTGTGGAACACAGGC[-/T]TACAGTGCTAGATGA | 84669 |
rs767123779 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, utr-variant-5-prime, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266034 | GCAACCACCATGTCT[C/T]TCAGTTCAACCCTGG | 84669 |
rs767142838 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60309069 | ATGCTCCAGGAGATT[A/G]TTCTGGGGAAAAAAA | 84669 |
rs767143443 | snp | C/T | 3.60783e-05 | 0.0042471 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231507 | TCCTTTTATTTCCCA[C/T]TCAACTACACATGTC | 84669 |
rs767145441 | snp | C/G | 1.66518e-05 | 0.00288542 | missense | USP32 | GRCh38.p7 | 17:60214655 | GGCGCATATCTTCCT[C/G]TTTAATGCGCAGCCT | 84669 |
rs767151846 | snp | G/T | 1.70472e-05 | 0.00291947 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266140 | TTTTTGTATTCTGAG[G/T]TATAATATATTTTAC | 84669 |
rs767166918 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242101 | GGATATCCAAATTCT[C/T]CTGCACCGTTTTTTG | 84669 |
rs767174346 | snp | C/T | 1.72353e-05 | 0.00293553 | intron-variant | USP32 | GRCh38.p7 | 17:60208233 | AGAGAAAAGATCTTT[C/T]ATTGGTAAAATGCAG | 84669 |
rs767186931 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256132 | TCGCTTGAGCCCAGG[A/T]GCATGAGTCCAGCCT | 84669 |
rs767222610 | snp | A/G | 1.64939e-05 | 0.0028717 | intron-variant | USP32 | GRCh38.p7 | 17:60180653 | CTGTAAGAGATAAGA[A/G]AGTGGAGGTATGTTA | 84669 |
rs767230689 | snp | A/G | 1.64836e-05 | 0.0028708 | missense | USP32 | GRCh38.p7 | 17:60198290 | TTACTAGCTTCCTGA[A/G]GTGGGAGTGGGCTCG | 84669 |
rs767230741 | snp | C/T | 1.7625e-05 | 0.00296854 | synonymous-codon | USP32 | GRCh38.p7 | 17:60211058 | AGTTCCACTCCAAAG[C/T]TCCTGCACTAAATCA | 84669 |
rs767236235 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60250891 | TTGCTTAATCTTCTT[A/T]AAGAAATAACCATGC | 84669 |
rs767236496 | snp | A/C | 3.46111e-05 | 0.00415985 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181672 | GCTCCTCCCCAAAGT[A/C]CGTGGGCTGCTATTA | 84669 |
rs767237764 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60321376 | ACTGATGCCCTGAGC[C/G]CATCATTATCAAGGA | 84669 |
rs767246841 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60294255 | TATGCAAATCAACTA[C/G]GTGAAATAAATGACA | 84669 |
rs767252493 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60214180 | CTCCTGACCTCTGGT[A/G]CTCCAGCCACCTCGG | 84669 |
rs767254005 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60262640 | GAGTTTTGTACCCAA[-/G]GCCCTTCAAGATACG | 84669 |
rs767256694 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60257441 | AGCCAGTTTTTAAAA[C/T]CTCACAGTGGAGAGA | 84669 |
rs767262696 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | USP32 | GRCh38.p7 | 17:60190626 | ATCCACAGCGATATA[A/G]GCATTTCCAATGAAA | 84669 |
rs767266172 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60273657 | GACCCAAAATCAGGA[C/T]TAAAAATTAGTCAAT | 84669 |
rs767274696 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60247386 | GGTTTCACCATGTTG[A/G]TCAGGCTGGTCTCGA | 84669 |
rs767279264 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60339246 | AAGTACACTAATCTA[G/T]CCTCAAAACAGTATG | 84669 |
rs767281985 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378504 | GTACACCAATGTTCA[C/G]AACAACATTATTCAC | 84669 |
rs767302297 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60309936 | GTAATCCAAGCTAGT[C/T]GGAAGTCTGAGGCAG | 84669 |
rs767304027 | snp | A/G | 1.67683e-05 | 0.00289549 | missense | USP32 | GRCh38.p7 | 17:60252426 | GCTGGTCTTAACCCC[A/G]GAACTATGTGACACA | 84669 |
rs767304058 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60396261 | TTTTTATTTTCTGTA[A/G]AGACAGAGTTTCTGT | 84669 |
rs767318717 | snp | C/T | 4.94197e-05 | 0.00497066 | missense | USP32 | GRCh38.p7 | 17:60198359 | TCTTTCTTCCGGGTA[C/T]GCACAGTACATGGAA | 84669 |
rs767346167 | snp | G/T | 3.30017e-05 | 0.00406199 | missense | USP32 | GRCh38.p7 | 17:60255203 | TTCAAAAACTCATTG[G/T]CAAGAACATTTTTCA | 84669 |
rs767350042 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60287986 | AGGCATGGTGGTGGG[C/T]GCCTGTAGTCCCAGC | 84669 |
rs767372301 | in-del | -/T | 5.78207e-05 | 0.00537653 | intron-variant | USP32 | GRCh38.p7 | 17:60269400 | ATTGATGAAAACTGA[-/T]TTTCTCTCTACATAG | 84669 |
rs767379974 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60355870 | AAGAAAAAAAAAAAA[-/G]AATGGCTGAACCTCT | 84669 |
rs767392429 | snp | C/T | 5.62762e-05 | 0.00530424 | intron-variant | USP32 | GRCh38.p7 | 17:60301551 | GAATTTTGAGATAAA[C/T]TATTCTGTACATAGA | 84669 |
rs767394591 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60187211 | TATGAGAGTCACGAG[G/T]CTCTCAAATGCTGCT | 84669 |
rs767432355 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60315336 | ACCCGGAAGGCAGAG[A/G]TTGCAGTGAGCCGAG | 84669 |
rs767440767 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60291217 | ATCTCTGAAATTCAC[A/T]TGCCCATTGGGAATC | 84669 |
rs767445276 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60228125 | CCGCCTCTAGCTTCA[A/G]ATGATTCTCCTGCCT | 84669 |
rs767449062 | in-del | -/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414854 | TTCTTTTCTTTCTTT[-/C]CTTTTTTTTTTTTTT | 84669 |
rs767455107 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60253972 | ATATGTTTTAAATAC[A/G]TAAAACTTAGTCATT | 84669 |
rs767478349 | snp | C/T | 4.95987e-05 | 0.00497965 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60294742 | CCACGTGGAGCATTC[C/T]TTCCATTTCTTCCCG | 84669 |
rs767480574 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60185059 | ATAGCCACATGATTA[C/T]GTGCAGTGGGTGTTG | 84669 |
rs767481485 | snp | A/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405099 | GAACCAGGGAGGTAG[A/T]GGCTGCAGTGACCCA | 84669 |
rs767486060 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60184810 | GTGAGACCCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 84669 |
rs767487136 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60283038 | ATTGAAATATAAAGT[A/G]TTGCAGAAATGCAAA | 84669 |
rs767493670 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60394573 | TGACCGCATGTGTCG[C/T]TTTCCAATGGGGTGC | 84669 |
rs767507152 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60332609 | GCCAAGATCATGCCA[C/T]TGCACTCCAGCCTGG | 84669 |
rs767532796 | snp | C/T | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422177 | TTTCCTCTCGGGGAG[C/T]CCCCACCACGGCGTA | 84669 |
rs767553931 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179189 | TCAGTGACGCTTTTG[C/T]CAAATGTCAGCTACA | 84669 |
rs767559855 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60342757 | GAGAGAATCTCCTCT[C/G]CTGGTTGCTAAGACC | 84669 |
rs767625645 | snp | A/C | 1.66996e-05 | 0.00288956 | missense | USP32 | GRCh38.p7 | 17:60214714 | ATGGTCTGCATTCGA[A/C]TAAAACAGCCTGTAT | 84669 |
rs767632088 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60330819 | ATCATAAGGAAAAGA[C/G]AGAGTTCCAAATTTA | 84669 |
rs767632156 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60351350 | ACAGGCATGCACCAC[G/T]ATGTCAGGCCCTTCC | 84669 |
rs767645771 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195847 | ATTCAAGTGAATTTC[C/T]CACTTGAATATATCA | 84669 |
rs767652365 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60307353 | TGATCTGCCTGCCTT[A/G]GTCTCCCAAAGTGCT | 84669 |
rs767657064 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60263097 | GGAACTATAGACATG[A/T]GCTACTGTGCCTGGC | 84669 |
rs767683690 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60252771 | TTGCATATGCTAGAT[C/T]TTAAATAACCAAAAC | 84669 |
rs767686907 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60349423 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCCAG | 84669 |
rs767707521 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306360 | AATAATTTTCTGGCC[A/G]GGCGCAGTGGCTCAT | 84669 |
rs767715730 | snp | A/C | 1.68576e-05 | 0.00290319 | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179228 | TCTCCCTCACCGCCA[A/C]GCTGTCTAGCAGCCA | 84669 |
rs767716411 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418628 | TCCTACAAAGGTCTA[A/G]TATCCAGCATCTGAA | 84669 |
rs767717762 | snp | C/T | 1.67818e-05 | 0.00289665 | synonymous-codon | USP32 | GRCh38.p7 | 17:60185475 | CAGGATGGGTGGAAG[C/T]CTCCAGAGATCCAGC | 84669 |
rs767728295 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60391517 | AGGTTTTTATGAAGG[A/C]ATGATAGGAGAAAAT | 84669 |
rs767751796 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182200 | AAAAATCCTGTAAGG[C/T]TTTAAACTTTTTGGT | 84669 |
rs767769636 | snp | A/G | 1.70664e-05 | 0.00292112 | intron-variant | USP32 | GRCh38.p7 | 17:60391855 | GCGGGCCTCCCAGGC[A/G]GCTCGCCCAGACCCC | 84669 |
rs767776821 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353288 | CAGGAAGAGAGCCCT[C/T]ACCAAAAACAAAACC | 84669 |
rs767777339 | in-del | -/AAGAA | 1.86385e-05 | 0.00305268 | intron-variant | USP32 | GRCh38.p7 | 17:60181764 | CTGTGAACAGGACAG[-/AAGAA]AAGATTCACAAATTC | 84669 |
rs767779682 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60292525 | ATCAGGCTAAATACT[A/G]ATCATCTTCCCCCTA | 84669 |
rs767797434 | snp | C/T | 1.65351e-05 | 0.00287528 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271461 | AGCGTTTCTCAAGAT[C/T]AATGATGTCTGATTC | 84669 |
rs767802358 | snp | C/T | 4.99272e-05 | 0.00499611 | intron-variant | USP32 | GRCh38.p7 | 17:60212138 | TAATTTCTTATCTAT[C/T]TAATTTATACCCATT | 84669 |
rs767822775 | in-del | -/C | 1.67217e-05 | 0.00289147 | intron-variant | USP32 | GRCh38.p7 | 17:60210987 | ATTAGGAATTAAATA[-/C]TTTTATATTATTTTA | 84669 |
rs767829952 | in-del | -/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60225952 | TGTGAAACTCAGTCT[-/C]AAAAAAAAAAAAAAA | 84669 |
rs767830468 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60262550 | GATTTTCAAAATAGT[A/G]TCAGCTGATCACTTG | 84669 |
rs767847952 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60337909 | TAAGATTAGACAAGA[C/T]GTACATGAACAATTA | 84669 |
rs767879834 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60386356 | CTACTAATTTTTAGT[A/T]CATAAATTAAAAAAA | 84669 |
rs767882612 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60301429 | CACTGTAATTTTAAT[C/T]TATATTTCTCTAATG | 84669 |
rs767887101 | snp | A/C/G | 3.29556e-05 | 0.00405918 | missense | USP32 | GRCh38.p7 | 17:60205637 | GTGAACATTTCATTT[A/C/G]TAGATGGCGAAGAGG | 84669 |
rs767899750 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328692 | ACCTGGGAGCTCCCT[A/G]AGCCAGGGCTATGAG | 84669 |
rs767905687 | in-del | -/TG | | | intron-variant | USP32 | GRCh38.p7 | 17:60329365 | ATCCCACAGAATTGT[-/TG]TGACTATTATATGCT | 84669 |
rs767911840 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60293843 | TCAAAAAGCCACCCA[A/C]AAGAAAATGGGCAGC | 84669 |
rs767941105 | in-del | -/AAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60357156 | CTGAGGAACAGAAAG[-/AAC]AACAAATGAAGAGGC | 84669 |
rs767944303 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191933 | GTAACTCTTTAAAAA[C/T]CAAGAACAGATTTCC | 84669 |
rs767959391 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373143 | GGCTACAGTAAGCCA[C/T]GATCACGCCACTTCA | 84669 |
rs767962683 | snp | A/T | 1.64746e-05 | 0.00287002 | missense | USP32 | GRCh38.p7 | 17:60219685 | CCATATTCACCCAGA[A/T]GTTAGACTGCTGTGT | 84669 |
rs767981128 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290797 | ATTAACCTCTAGGGA[A/G]GGAGGGGAGAGGGCT | 84669 |
rs767989882 | snp | C/T | 1.69703e-05 | 0.00291288 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265517 | AGAAAACAGTGAATA[C/T]ACTTTTAATTTTGTT | 84669 |
rs768008966 | snp | C/T | 3.29707e-05 | 0.00406008 | synonymous-codon | USP32 | GRCh38.p7 | 17:60345595 | CTTCAGTCGTTTTAG[C/T]TCTACATCTGTAACT | 84669 |
rs768026291 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60247445 | TCGGCCTCCCAAAGT[C/G]CTGGGATTACAGGCA | 84669 |
rs768028160 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60348839 | TGCTTGTGGTAGGAA[-/G]GGGGGGGTTCATGGT | 84669 |
rs768032258 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60253366 | TCATACAAAAAGTTC[A/G]TACACTCAACATGTG | 84669 |
rs768033343 | snp | A/C | 2.26201e-05 | 0.00336296 | intron-variant | USP32 | GRCh38.p7 | 17:60219824 | AGAGATCACTAAAAA[A/C]AGAAACAAAACTTGC | 84669 |
rs768061653 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60224042 | AATGGGGGCTAGATC[C/T]TATTGTATCTATGAA | 84669 |
rs768114842 | snp | A/C | 1.64741e-05 | 0.00286998 | missense | USP32 | GRCh38.p7 | 17:60183329 | AGTGGTTTATGCTGG[A/C]AGAGAGCCGGGTCTC | 84669 |
rs768156721 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271382 | CGAATAGGTGGTGAA[A/G]CCAATGGGCCAAATG | 84669 |
rs768184021 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60254028 | ATTTATTCCAACACA[C/G]ACGTGTTGCAGACAA | 84669 |
rs768191003 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60366746 | CTCAAAAAAAAGTTG[-/G]GTTTTTTTTTTTTCA | 84669 |
rs768200574 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60374194 | GTCTCCAAAAAAAAA[A/G]GAAAAAAGACATAAA | 84669 |
rs768200850 | snp | A/C | 1.67823e-05 | 0.0028967 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183418 | TGATTTTATCCACCG[A/C]CCATTTACAAATTGA | 84669 |
rs768241150 | snp | C/T | 3.295e-05 | 0.00405881 | missense, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179321 | ACTGCTTGTGTCTGC[C/T]ATCTTTTTGCCATCA | 84669 |
rs768252863 | snp | C/T | 1.69436e-05 | 0.00291058 | intron-variant | USP32 | GRCh38.p7 | 17:60198230 | CTAGAGTTTGGAAAC[C/T]ACAGGTTTAGATGGA | 84669 |
rs768267908 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178787 | TGATCTTGCTTTCTC[C/T]ATCTTGTCAATATAA | 84669 |
rs768300669 | in-del | -/CT | | | intron-variant | USP32 | GRCh38.p7 | 17:60345973 | GACAACAGAGCGAAA[-/CT]CTGTCTCAAAAAAAT | 84669 |
rs768304663 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60362861 | AAAAAACAAAAAACA[C/T]CTTAGTCAAAAGGCA | 84669 |
rs768311245 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60342281 | CAAATATTGCTGCCC[A/G]ATCCTTCCTCTGGAA | 84669 |
rs768324709 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60238428 | ATCTCAGCACTTTGG[C/G]AGGCTGAGGCAGGCG | 84669 |
rs768342871 | snp | C/G | 1.71991e-05 | 0.00293245 | intron-variant | USP32 | GRCh38.p7 | 17:60391831 | TACCCACCCTCCAGG[C/G]TGCCCGTCGCGGGCC | 84669 |
rs768350161 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60287346 | TTCAAGATATCTGGC[A/C]CTTTTAGGCCAAAAC | 84669 |
rs768350949 | snp | A/G | 3.30589e-05 | 0.00406551 | missense | USP32 | GRCh38.p7 | 17:60212096 | TCATATCTTTGTTGC[A/G]AACTGGAAGGACAGA | 84669 |
rs768378147 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60299115 | TACTCTAGCCTGGGC[C/T]ACAGAGTAAGGCTCT | 84669 |
rs768391055 | in-del | -/A | 1.724e-05 | 0.00293594 | intron-variant | USP32 | GRCh38.p7 | 17:60208222 | ATCACTAGTAAAGAG[-/A]AAAGATCTTTTATTG | 84669 |
rs768392859 | snp | C/T | 1.79329e-05 | 0.00299435 | missense | USP32 | GRCh38.p7 | 17:60209395 | ACTTCCCAGTCTGGT[C/T]GCCCATCACTGTCCT | 84669 |
rs768407456 | in-del | -/ACAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60195957 | ATGGTACCACCATTC[-/ACAA]ACAATTGTTCAGGGT | 84669 |
rs768445207 | snp | A/C/G | 4.96778e-05 | 0.00498366 | synonymous-codon, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265457 | TTCTACAATATCAGA[A/C/G]AGATCCATATGTAAT | 84669 |
rs768463863 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60372373 | TACACAAACTTAGAT[G/T]GTATAGACTACTACA | 84669 |
rs768464528 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60343780 | CTCACGCCTGCAATC[A/C]CAGCACTTTGGGAGG | 84669 |
rs768478538 | in-del | -/TTTG | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420066 | TTTTATTTTATTTAT[-/TTTG]TTTATTTTATTTTAT | 84669 |
rs768491461 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60189863 | TTTAACAGAGAGATG[C/T]TTATTGATATGTCAT | 84669 |
rs768505380 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60311959 | TAAAGGGTTATCCCA[C/T]AGTTCCTTAGGGGAA | 84669 |
rs768511776 | snp | A/G | 1.65411e-05 | 0.00287581 | missense | USP32 | GRCh38.p7 | 17:60205502 | CTGTCAGGAAGAGAT[A/G]GCATGTGACCATTAA | 84669 |
rs768514353 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60354468 | TTCACTGCCAAAGTG[G/T]GCTAAGAATTTACAA | 84669 |
rs768524439 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60190952 | GGAAGATGTGAACTT[C/T]ATGGCAAATAAATGA | 84669 |
rs768527392 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60361058 | TGCTTGAACCTGAGA[A/G]GCGGAGATTGAAGTG | 84669 |
rs768530857 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60230527 | CGGTTCTACCACATG[C/G]TTTTAACATGGTACA | 84669 |
rs768533033 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60238803 | GCGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 84669 |
rs768534537 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60278571 | TAGGACAGAAAGACA[A/G]AAAAGCAGTTGTGTT | 84669 |
rs768542527 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60323178 | GAAATATATATCCAC[A/G]CAAAGGTATACAAAT | 84669 |
rs768544066 | snp | C/G/T | 3.29458e-05 | 0.00405857 | missense | USP32 | GRCh38.p7 | 17:60183305 | GAGAGCTCATCCCCC[C/G/T]GGGGTGTGAGTGGTT | 84669 |
rs768612091 | in-del | -/TTTTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60369752 | AGTTCTACACAATGA[-/TTTTT]TTTTAAGAGACAGGT | 84669 |
rs768624257 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60357028 | AGAAGTATGAGGTTG[C/T]AGTGAACTATGATTG | 84669 |
rs768624890 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308860 | TCTAAACCCAGGAGG[C/G]GGAGGTTGCAGTGAG | 84669 |
rs768633869 | snp | C/G | 4.94287e-05 | 0.00497111 | missense | USP32 | GRCh38.p7 | 17:60183351 | CCGGGTCTCTTGGTA[C/G]CAAAAAAGCACTTGG | 84669 |
rs768635949 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60269830 | TTAATGGCTAAAATG[A/T]CTATTTTTGAAGTCA | 84669 |
rs768670688 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60257052 | TAATGGAGTTGATAA[C/T]GTTACCAAGCAAAGG | 84669 |
rs768676852 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60274648 | AATTGTCAACCTCCA[A/C]TTCTGTATCACGTGA | 84669 |
rs768692573 | snp | C/T | 1.67393e-05 | 0.00289299 | missense | USP32 | GRCh38.p7 | 17:60219751 | AGCGGGGAAATAATT[C/T]CAGCTCTGGGATGTC | 84669 |
rs768712706 | snp | C/T | 6.81803e-05 | 0.00583828 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181324 | TAATAAACCACTTAC[C/T]GAAATTGCATATAGA | 84669 |
rs768731430 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60398184 | AGCTTGGGCAACATA[C/T]GGAGACTCTGTCTCT | 84669 |
rs768752626 | snp | A/G | 1.65466e-05 | 0.00287628 | missense | USP32 | GRCh38.p7 | 17:60214759 | TTTAAAGGTGCATTC[A/G]GAGAAGGTACATTTC | 84669 |
rs768760833 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60273243 | CTCCGAAAGTGTGGG[A/G]ATTACTTACAGGCAT | 84669 |
rs768763479 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60258724 | CTGGCAGTTTGAATG[-/T]TTACAGGACATTCCA | 84669 |
rs768782432 | snp | C/T | 1.65048e-05 | 0.00287265 | intron-variant, missense | USP32 | GRCh38.p7 | 17:60219642 | CCTCTCGGTAAATGC[C/T]GAGGAAACATTCTCA | 84669 |
rs768789624 | snp | C/T | 1.72311e-05 | 0.00293518 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294827 | GAAAGATAGAATAAA[C/T]TAATCTTAACAAAGA | 84669 |
rs768812550 | in-del | -/GACAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60196637 | GAGACCAGCCTGGCC[-/GACAT]GACATGGTGAAACCC | 84669 |
rs768842550 | snp | C/T | 1.6686e-05 | 0.00288838 | missense | USP32 | GRCh38.p7 | 17:60214696 | TATTCGTGAATTTCC[C/T]TGATGGTCTGCATTC | 84669 |
rs768868274 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60228973 | CACCTGGTTAAATTA[A/G]GTTTCAAAAGAAAAT | 84669 |
rs768883281 | snp | A/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408661 | GGGATTACAGGCATG[A/T]GCCACCATGCCCGGC | 84669 |
rs768909965 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60376723 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 84669 |
rs768915372 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60421882 | CGGGACTTGCCCGCG[G/T]CTCAGCGCCTCCTGT | 84669 |
rs768922820 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60241624 | TCATTGTGCTTTTAA[C/T]TTGCCTTCTCTGAGG | 84669 |
rs768933073 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403800 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCGGGAG | 84669 |
rs768935256 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60332036 | TTGCTTGAGCTCAGG[A/G]GTTCAAGATCAGTTT | 84669 |
rs768956006 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60242881 | TCTCTGCATTTCCCT[A/G]TACAATTTAGGAATA | 84669 |
rs768963519 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | USP32 | GRCh38.p7 | 17:60181434 | TGCTGTAGCCATTGC[C/T]ACATGCTTCATGCTC | 84669 |
rs768967863 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60186302 | CAGGGGTGCTGATAG[C/T]AAGCCATTTACTTTT | 84669 |
rs768968478 | snp | C/G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60280241 | AGCTGGGATTACAGG[C/G/T]GTCCACCACCACACC | 84669 |
rs768990170 | snp | C/T | 8.92403e-05 | 0.00667924 | intron-variant | USP32 | GRCh38.p7 | 17:60211556 | GCTTAGCTGTAGTAA[C/T]ATGCCATGGCACAAA | 84669 |
rs768995042 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295376 | TATTCAGAGGAAAAG[A/C]AAATGACAAAATCAT | 84669 |
rs768996857 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60421257 | CTTACAACAACAACA[A/G]CGACAACAATAACAA | 84669 |
rs769039317 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60400594 | AGAGCTTTGGACATA[C/T]TACATTTGAGATGTC | 84669 |
rs769045110 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60395727 | AAAGGGTTATCCATA[C/T]AAAGATTTAAAGCAC | 84669 |
rs769055155 | in-del | -/T/TT/TTT | 0.592526 | 0.159497 | intron-variant | USP32 | GRCh38.p7 | 17:60255298 | AACATCTTTTTTTTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 84669 |
rs769058586 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60369423 | GCAAGACCCCTACCT[-/A]AAAAAAAAAAAAAAA | 84669 |
rs769066605 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60368471 | AAAATCTTTTCAACA[A/G]AAGACTCTGCTTCAA | 84669 |
rs769099704 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60283782 | GGCATTTATTAAAAT[C/G]AATCTGAGGTTTCAG | 84669 |
rs769122586 | snp | A/G | 1.76278e-05 | 0.00296877 | intron-variant | USP32 | GRCh38.p7 | 17:60208009 | ATAATTGAGAAAAAT[A/G]TCATCTTTGGAGGAT | 84669 |
rs769140175 | snp | G/T | 1.73601e-05 | 0.00294614 | intron-variant | USP32 | GRCh38.p7 | 17:60183158 | GCATAAGGCCCCCAG[G/T]CCTCACCTTTCGGGC | 84669 |
rs769140821 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60212901 | TGGGACTACAGGCAC[A/G]TGCCACCACACCCAG | 84669 |
rs769148126 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60278753 | CATTTCAGTCACAAC[A/G]TAGACATTTCAAAGA | 84669 |
rs769151064 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60317260 | GGCTCATGCCTATAA[A/C]CCCAGCACTTTGGGA | 84669 |
rs769154232 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60390938 | AAAAATTAAGACATT[C/G]CGGCCATAAACTGTG | 84669 |
rs769164414 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408671 | GCATGAGCCACCATG[C/T]CCGGCCAATCTGGCT | 84669 |
rs769177824 | in-del | -/CA | 1.70087e-05 | 0.00291617 | intron-variant | USP32 | GRCh38.p7 | 17:60391863 | CCCAGGCAGCTCGCC[-/CA]GACCCCTCCCCCCTC | 84669 |
rs769190238 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60347930 | GATCCAGACCATCCT[A/G]GCTAGCACAATGAAA | 84669 |
rs769192819 | in-del | -/TTAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60193064 | GTTGACAGCTCAATG[-/TTAC]TTACCCTAATCCATT | 84669 |
rs769202404 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60316128 | TGGCCTTTTTGAAGA[C/G]ATCAACCACTCTGCT | 84669 |
rs769204841 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60303861 | CCAAAACGAAACAAA[A/C]GGGGGAAAATGTGAG | 84669 |
rs769209188 | snp | C/T | 1.67652e-05 | 0.00289522 | synonymous-codon | USP32 | GRCh38.p7 | 17:60219758 | AAATAATTCCAGCTC[C/T]GGGATGTCTGTCTTG | 84669 |
rs769214208 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195484 | CTGGGATTACAGGCA[C/T]GTACCACCATGCCCG | 84669 |
rs769223443 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60345701 | CTAAGAAAAATTGAG[C/G]CTAGGCACAGTGGCT | 84669 |
rs769226436 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60360915 | AGGCAGATCGCTTGA[A/G]GTCAGGAGTTCGAGA | 84669 |
rs769256708 | snp | C/T | 1.64917e-05 | 0.00287151 | missense | USP32 | GRCh38.p7 | 17:60223452 | GCTGATTATCAATAG[C/T]CCCTGGTTTCTGAGG | 84669 |
rs769272355 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378784 | GGGCTGGGGAAAAAA[A/C]GGGATAGAGAATTTC | 84669 |
rs769321824 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60360502 | CGTATCTACTAAAAA[C/T]ACAAAAGTTAGCCAG | 84669 |
rs769332343 | in-del | -/TT | | | intron-variant | USP32 | GRCh38.p7 | 17:60240576 | CGCTGTGCTGGGGCA[-/TT]TTCCTACAATGGTTT | 84669 |
rs769346748 | snp | G/T | 1.66969e-05 | 0.00288932 | intron-variant | USP32 | GRCh38.p7 | 17:60255132 | AAGATGTAGAAGTAC[G/T]GGTACTACTACCCTC | 84669 |
rs769362183 | snp | C/T | 3.50896e-05 | 0.0041885 | missense | USP32 | GRCh38.p7 | 17:60211014 | TTTAACCTGCTTACC[C/T]GAAGCTTTAATGGGG | 84669 |
rs769365394 | in-del | -/TAACTC | | | intron-variant | USP32 | GRCh38.p7 | 17:60400654 | AGAGAGTTAGATATT[-/TAACTC]TGAAGTTAGAAAAGG | 84669 |
rs769365761 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60191067 | CTGGTGTAACACCTA[A/G]CTCCTTGTCTGTAAA | 84669 |
rs769370074 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60354818 | TGGGAGGCTGAGGCA[A/G]GCAGATCGCTTAAGG | 84669 |
rs769391071 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60372438 | GGCTACAAACCTACA[C/T]AGCATATTACTGTAC | 84669 |
rs769406363 | snp | A/G | 1.64789e-05 | 0.0028704 | intron-variant | USP32 | GRCh38.p7 | 17:60236243 | TTCTAACCATCCTCT[A/G]TATGTACAAAAGAAA | 84669 |
rs769407807 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60301896 | AGCCTAGAATAGACT[A/G]TGACTACTGTAAAAT | 84669 |
rs769448540 | snp | G/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60415858 | TTTGTTTGTTTTTTT[G/T]AGATTGAGTCTCACT | 84669 |
rs769452992 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60186323 | ATTTACTTTTAATCA[C/G]AAAGCCAGAGCATTA | 84669 |
rs769459560 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60224777 | AACAGAGTGACACCC[C/T]GTCTCTTTAAGTAAA | 84669 |
rs769469703 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60223618 | GGATAGAATCTCTTA[-/T]TTTTAGTTATTATAC | 84669 |
rs769478716 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60318718 | GAGTAGAACCAAAAC[A/C]CAAAAATTTTACTGA | 84669 |
rs769485131 | snp | A/G | 3.81047e-05 | 0.00436473 | intron-variant | USP32 | GRCh38.p7 | 17:60206975 | ACAACTCTTAGACAA[A/G]TATTTAAAGGAGCAA | 84669 |
rs769487199 | snp | A/G | 5.00471e-05 | 0.00500211 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266117 | GAAACTCTTATGGAG[A/G]AAAATCATTTTTGTA | 84669 |
rs769523215 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60367774 | ATGGCCCCACTGTAC[-/T]TCCAGCCTGGGTGAC | 84669 |
rs769548004 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60229772 | ATTTATACTCACTTC[C/T]ATATTCCATTTATAT | 84669 |
rs769564746 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60286990 | CCTTCTCTGATAAAA[A/C]TACAAAAAATTTAGC | 84669 |
rs769570851 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60304288 | ACTAAAGGAAAAAAA[C/T]TCAACCATAAGTTCT | 84669 |
rs769571694 | snp | C/G | 1.75807e-05 | 0.0029648 | intron-variant | USP32 | GRCh38.p7 | 17:60185409 | GTTTGTTCATGTCTT[C/G]TTTCTTTTATGCCAG | 84669 |
rs769612921 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60183686 | AGTGTGGCACAGCCA[C/T]GTGACTGCGCAGTGG | 84669 |
rs769619439 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60328194 | ATAGACCAATCAGTG[C/T]ATACTTCCTCCCCTC | 84669 |
rs769642439 | snp | C/T | 3.29489e-05 | 0.00405874 | missense | USP32 | GRCh38.p7 | 17:60226153 | CTTCGACCTGCTCCA[C/T]AGGATGGGCTGCAGT | 84669 |
rs769652298 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60300925 | CTAATCTTGAAATTT[C/T]ATATAAATGGAATCA | 84669 |
rs769660216 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60392210 | CCTCCCTCTCCTTCC[C/T]TCCTCACGCCCTCTT | 84669 |
rs769680159 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60400839 | CAGCCTAGGCAACAT[C/T]GGTAGACCTAGTCTC | 84669 |
rs769682417 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60399762 | AAAATTGGAAGGAGA[A/G]AATGAAGCAGACTTT | 84669 |
rs769688411 | snp | A/C/G | 3.32459e-05 | 0.00407702 | missense, stop-gained | USP32 | GRCh38.p7 | 17:60209441 | GCTTTTCATGGACTC[A/C/G]ATTAAGATCTTCATG | 84669 |
rs769692912 | snp | A/G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60248181 | TTTGGTTTTTTCCTT[A/G/T]TATCACTTTCTCATA | 84669 |
rs769701356 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60263272 | AACATAGCCCTGATC[A/T]CACTTGTCTATCTTT | 84669 |
rs769726271 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60314752 | TCAAAGAAACTCATA[C/T]GTAAGATAAACAAAA | 84669 |
rs769729040 | snp | A/C | 1.64779e-05 | 0.00287031 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266008 | GGTTGTCCTTCCAGA[A/C]TTCTAAAAGTGCAAC | 84669 |
rs769744701 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60237304 | GCTATGCCCAGCTAA[-/T]TTTTTTTTTTTTTTT | 84669 |
rs769764684 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60338384 | ATTTGTTTGAGAGGA[A/G]TAGATGTTCTGAGGA | 84669 |
rs769764728 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179348 | ATCAGTCTTTGGCAG[A/G]AATTGTGCATAGTCT | 84669 |
rs769766474 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | USP32 | GRCh38.p7 | 17:60181451 | CATGCTTCATGCTCA[C/T]AAAGGAATCCATTGG | 84669 |
rs769781914 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60246848 | TTTTTTTGAGCAATG[C/T]CTATTCAGATCACTT | 84669 |
rs769789669 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60385579 | AGAAGCAGTGGCTCA[C/T]GCCTATAATCTCAGC | 84669 |
rs769793443 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60360737 | GTAGATGATAATGTG[-/A]AAAAAAATGTGGTTG | 84669 |
rs769810268 | snp | C/T | 1.66874e-05 | 0.0028885 | synonymous-codon, intron-variant | USP32 | GRCh38.p7 | 17:60391898 | TCTCCTCAGCGCCTC[C/T]TCGTAGCTGAGGAAT | 84669 |
rs769833660 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258525 | GATGGATTTAACAGC[C/G]TGACAAAAGTGACTT | 84669 |
rs769840508 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60243285 | CAGGGTTTTCTACAC[A/G]TAGGATCATGTTATC | 84669 |
rs769846466 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178738 | AAATTGAAAAATCCT[C/T]GTCCATGCCTTAAGA | 84669 |
rs769857407 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60388683 | AAAATATTTAAGAAA[C/G]ATAGATTCAAGCCAA | 84669 |
rs769897348 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60333698 | AAAGAAAAGAGAGGA[A/G]AGGAGAGGGGAGGGG | 84669 |
rs769898127 | snp | C/T | 3.4343e-05 | 0.00414371 | intron-variant | USP32 | GRCh38.p7 | 17:60391838 | CCTCCAGGCTGCCCG[C/T]CGCGGGCCTCCCAGG | 84669 |
rs769899063 | in-del | -/C | 3.63875e-05 | 0.00426526 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391987 | CTGATCTCGCCCCCA[-/C]CCCCCCTCCCGCCTT | 84669 |
rs769899895 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60367867 | CCTCTGTACCAAACA[C/T]GTACAGGCTTTTTTT | 84669 |
rs769917658 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412118 | AATTTACCTGACTGG[A/C]CCCAACAAGCCCAAC | 84669 |
rs769931191 | snp | A/C | 8.6003e-05 | 0.00655699 | intron-variant | USP32 | GRCh38.p7 | 17:60255286 | CACTCATGTTAGGAA[A/C]ATCTTTTTTTTCTTT | 84669 |
rs769946053 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60230094 | GCTGGGGTTACAGGC[A/G]TGAGTCACTGCGCCC | 84669 |
rs769948008 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60235897 | ATATGCAGGTACCCC[C/T]GTACCCAATATTATC | 84669 |
rs769959819 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60326652 | TAGCAGCAGCACATG[C/G]AATTTGTGGATCTCA | 84669 |
rs769962817 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60397422 | GGCTGGAGTGCAGTG[C/G]TGTGATCATAACTCA | 84669 |
rs770004828 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60327540 | GCCCGCCCGCCAGCA[-/G]AAGAGCAGCACGGTT | 84669 |
rs770015605 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395927 | AAGCACCTAATTTAT[C/G]TATAACTTCATTGCT | 84669 |
rs770018687 | snp | C/T | 1.7959e-05 | 0.00299652 | intron-variant | USP32 | GRCh38.p7 | 17:60211566 | AGTAATATGCCATGG[C/T]ACAAACAGTTACTTA | 84669 |
rs770018843 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60350935 | AAAAATAGGACAAGA[C/G]AGACACGAGAACCTA | 84669 |
rs770036006 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60244615 | TATGGATCTTAACAT[A/G]GTCTACTTTATTGTT | 84669 |
rs770082982 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60417958 | CACGTCCGGCTAATC[-/T]TTTTTTTTTTTTTTT | 84669 |
rs770113666 | snp | A/G | 1.6563e-05 | 0.00287771 | intron-variant | USP32 | GRCh38.p7 | 17:60212119 | AGGACAGATAGGAAT[A/G]TGTTAATTTCTTATC | 84669 |
rs770115182 | snp | C/T | 4.94181e-05 | 0.00497057 | missense | USP32 | GRCh38.p7 | 17:60205610 | CGGGGTAGGTCCCCA[C/T]TGGTAGTTAGGGTGA | 84669 |
rs770145909 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60319071 | CTAAAAGTTGACTGC[A/G]TGTTATGAGGGTTTA | 84669 |
rs770161251 | snp | C/G | 1.74221e-05 | 0.00295139 | missense | USP32 | GRCh38.p7 | 17:60208192 | TACCGTACAGGGGTA[C/G]TACCATCTAACTTAA | 84669 |
rs770182944 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60236531 | AATTAATTAATTACA[-/T]TTTTTTGCAGAATGT | 84669 |
rs770235049 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60259539 | CTGGCCAGCCACTAA[A/C]CTGAACTGGAATAAG | 84669 |
rs770245478 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230583 | GAATATGGGCTTTTC[-/T]TTGCTTCTCTTCCAA | 84669 |
rs770249052 | snp | G/T | 1.64751e-05 | 0.00287007 | missense | USP32 | GRCh38.p7 | 17:60190612 | GCTGTGGGATCCCAA[G/T]CCACAGCGATATAGG | 84669 |
rs770251329 | snp | C/T | 1.65086e-05 | 0.00287298 | missense | USP32 | GRCh38.p7 | 17:60208726 | AAGGGTCAAATCGGA[C/T]ACTTATATGCCCACA | 84669 |
rs770272642 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60180762 | TGAAAAAATATTTTA[A/G]AACCCTCTAACTTTT | 84669 |
rs770283366 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60421668 | GCGCTGCTGCCGCGC[C/T]AGGGGCGAGGGTCCC | 84669 |
rs770317058 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60226445 | TAGACAAAACAGACT[G/T]TGAAGGATTTTGTGC | 84669 |
rs770324136 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60284864 | ATAGTCATTCCCCTC[A/G]CCTTGGACTGCTTTA | 84669 |
rs770341249 | snp | C/T | 6.63042e-05 | 0.0057574 | intron-variant | USP32 | GRCh38.p7 | 17:60192828 | ACTAAAGTAATTCTT[C/T]TGCAGGTCACTTTAC | 84669 |
rs770342074 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60253534 | ACTTTGGGAGGCTGA[A/G]GCGGGCAGATCACTT | 84669 |
rs770343245 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60253287 | ACTGAATATGTTCGT[A/G]TACAAACAGCATATG | 84669 |
rs770346187 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60379901 | ATGCTAAATTTGTGC[A/T]TAAAACAGTCCAATG | 84669 |
rs770351718 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60329367 | TCCCACAGAATTGTT[G/T]ACTATTATATGCTAG | 84669 |
rs770373388 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405606 | ATCGCTACAAAAATA[C/T]AAAAATTAGCCAGGC | 84669 |
rs770376590 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179180 | GCTTGCCTTTCAGTG[A/G]CGCTTTTGCCAAATG | 84669 |
rs770379876 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60263528 | ACATGGAAATGAAGC[A/C]GCTAAATGATCTTGT | 84669 |
rs770388437 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60357165 | AGAAAGAACAACAAA[A/T]GAAGAGGCCAGGCAC | 84669 |
rs770400000 | snp | A/C | 3.31636e-05 | 0.00407194 | intron-variant | USP32 | GRCh38.p7 | 17:60226003 | CTATCCAGGGGGAAT[A/C]AACCAATAAACCTCA | 84669 |
rs770401337 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60363606 | ACTTCCCACTCTCAC[C/T]CTCCTTAGTAGCTGG | 84669 |
rs770440659 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60337814 | TGAGCCTGGGAGGTC[A/G]AGGCTACAATGAGCC | 84669 |
rs770446456 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60191124 | AAGTTTACAGGGGCC[A/G]GGCATGGTGGCTCAT | 84669 |
rs770455497 | snp | A/C | 1.68315e-05 | 0.00290094 | intron-variant | USP32 | GRCh38.p7 | 17:60223388 | AAGAGAATAATTTTA[A/C]GTTTAGATGTAAAAT | 84669 |
rs770487678 | snp | A/G | 1.65151e-05 | 0.00287355 | missense | USP32 | GRCh38.p7 | 17:60223566 | AAACATCTGCCCCTG[A/G]TGTGGCAGAATACAG | 84669 |
rs770496834 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60248236 | TTCAAAAAGTCAGCT[A/G]TTTATCACATTGTGG | 84669 |
rs770515534 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60192801 | CTGTATAATATCTAA[A/C]GCTGAAATTCTACTA | 84669 |
rs770538015 | snp | C/T | 3.29484e-05 | 0.00405871 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183247 | CCCAGCCGAACTCTG[C/T]GCATCCACTTTCTTC | 84669 |
rs770539190 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393963 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 84669 |
rs770545534 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon | USP32 | GRCh38.p7 | 17:60222481 | TTCTGGGACCATTTC[A/G]TAGTCTCTTCCATGA | 84669 |
rs770562275 | snp | G/T | 1.65102e-05 | 0.00287312 | intron-variant | USP32 | GRCh38.p7 | 17:60214786 | TTTCCTATGGTTACA[G/T]TAATCACAGTAAGAA | 84669 |
rs770564979 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60400988 | CATAGCAAAACCCCA[C/T]CTCTACAAAAAGATT | 84669 |
rs770567790 | snp | A/G | 1.66696e-05 | 0.00288696 | synonymous-codon, intron-variant | USP32 | GRCh38.p7 | 17:60391916 | GTAGCTGAGGAATCC[A/G]ATCCGTGACTCCTTG | 84669 |
rs770572292 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416244 | AGATGGGCAGATTTC[A/G]TATCTATGAGGGAAA | 84669 |
rs770624674 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60241227 | TGGTCTCGAACTCCT[A/G]ACCTCAACTGATTCA | 84669 |
rs770632869 | in-del | -/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404305 | TATATGCAAGTGTTC[-/T]TTTGTGCTATTCTTG | 84669 |
rs770679494 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60375643 | GAGTCTCGCTCTGTC[A/G]CTCAGGCTGGAGTGC | 84669 |
rs770681490 | snp | C/T | 2.0658e-05 | 0.00321381 | intron-variant | USP32 | GRCh38.p7 | 17:60252352 | AAGTATGTGAAATTT[C/T]AACTATATAATTGAA | 84669 |
rs770724238 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60273465 | ACTCTAAACTTGTCC[A/C]AACAAAGCTTACAAA | 84669 |
rs770728335 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60235319 | TTATCTACCTACAAG[A/G]TCCAGGAAGTCATTT | 84669 |
rs770734475 | in-del | -/CA | | | intron-variant | USP32 | GRCh38.p7 | 17:60268582 | AACAAGACCCTGTCT[-/CA]AAAAAAAAAAAAAAA | 84669 |
rs770747867 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60339478 | ATCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 84669 |
rs770748357 | snp | A/C | 2.15051e-05 | 0.00327904 | missense | USP32 | GRCh38.p7 | 17:60211052 | CTTCTGAGTTCCACT[A/C]CAAAGTTCCTGCACT | 84669 |
rs770752546 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60239882 | GGGATTACAGGAGCC[C/T]GCCACCAGGCCTGGC | 84669 |
rs770763522 | snp | G/T | 0.000362349 | 0.0134552 | missense, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179370 | GCATAGTCTATCCCC[G/T]GCTGCTCATAGAAAA | 84669 |
rs770779564 | snp | A/C | 1.66999e-05 | 0.00288958 | missense | USP32 | GRCh38.p7 | 17:60214707 | TTCCTTGATGGTCTG[A/C]ATTCGACTAAAACAG | 84669 |
rs770805905 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60236589 | CAGCCTTATTGAGGA[A/G]TAATTTACATATATA | 84669 |
rs770812905 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60289838 | CAGCTCTAATCCTAA[C/T]AGACATGCTAAAGAA | 84669 |
rs770849727 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60204957 | TAAAAAAAAGAAGTC[-/T]TTTTTTTTTTTTTTT | 84669 |
rs770867343 | snp | A/G | 1.83515e-05 | 0.00302909 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231478 | TGTAAATTCAGAGAA[A/G]AGAGGTGTTTCATTC | 84669 |
rs770874415 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258536 | CAGCGTGACAAAAGT[A/G]ACTTTGTTGTTGATC | 84669 |
rs770901257 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60341836 | TTTTAGCTTCCTTGC[A/G]ATGGGTTCGAACATA | 84669 |
rs770923136 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60186701 | AGGAATTAAGTATAA[C/G]AAAGGACAGAGAGCA | 84669 |
rs770923244 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60368530 | ATTGCGGTTGGGGGG[C/T]GGGGGAAACGAGGGG | 84669 |
rs770956847 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60399463 | AGTTTGAGACCAGCC[G/T]GGGAAACATAGCAAG | 84669 |
rs770959871 | snp | A/G | 1.66189e-05 | 0.00288256 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60269531 | CTATGTGATTGTCAC[A/G]ATTTTCATCAAAAGC | 84669 |
rs770973607 | snp | C/T | 1.66272e-05 | 0.00288328 | intron-variant | USP32 | GRCh38.p7 | 17:60212135 | TGTTAATTTCTTATC[C/T]ATCTAATTTATACCC | 84669 |
rs770981756 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60244778 | ATAGGGTTACAGGCA[C/T]GCACCACCACGCCAG | 84669 |
rs770989474 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60383909 | AAGGAATAACAAGAT[A/C]TGGTTTGGATTTTAA | 84669 |
rs770996107 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60396657 | CCTAAAATTGGCAAC[A/G]TTTCAACAGGAGCCA | 84669 |
rs771004726 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60285280 | TATTTTAAGCAAAAT[A/T]ATTTTTTAAAAGGCT | 84669 |
rs771008665 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60397970 | TAGGTTAAGATAAAA[C/G]TTTTTCACATGGTGG | 84669 |
rs771020614 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60246307 | GCCTATCTCACTTAA[C/T]GTAATGACCTCCGGT | 84669 |
rs771049907 | snp | A/C/G | 3.39583e-05 | 0.00412046 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266137 | TCATTTTTGTATTCT[A/C/G]AGGTATAATATATTT | 84669 |
rs771052805 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60305438 | CTCGTGGGGATCTGC[C/T]CCCATGATCCAAACA | 84669 |
rs771059801 | snp | A/G | 1.65436e-05 | 0.00287602 | intron-variant | USP32 | GRCh38.p7 | 17:60226021 | CCAATAAACCTCAGG[A/G]GAATAGGTCATATTT | 84669 |
rs771075446 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60286346 | TCTTGAGGTAAAATT[A/T]TCCTGGATTTAGCCT | 84669 |
rs771080582 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60298219 | AATATTCATGGCCCC[-/T]CCGATAAGCTGTTGA | 84669 |
rs771083402 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60196952 | TTGAGAGGCCGAGGT[A/G]GGTGGATTACTTGAG | 84669 |
rs771103867 | snp | G/T | 1.65449e-05 | 0.00287614 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265419 | AGACTCACCTTTGTG[G/T]TGTCATGTGCATTCA | 84669 |
rs771108792 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60261418 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACTTAAG | 84669 |
rs771114310 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60399290 | ATAAGTATAATAGTA[C/T]ATCAGTTGTTCTACA | 84669 |
rs771126399 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60390731 | CGTCTTTTAATCTAA[-/T]TACCATTTTATATCC | 84669 |
rs771136624 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60292449 | TGATATCCAACCCCC[C/T]AACCTGCTTCTCCAT | 84669 |
rs771154344 | snp | A/T | 1.64749e-05 | 0.00287005 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205618 | GTCCCCATTGGTAGT[A/T]AGGGTGAACATTTCA | 84669 |
rs771193402 | snp | C/G | 1.64741e-05 | 0.00286998 | missense | USP32 | GRCh38.p7 | 17:60345521 | TCCCCAAGCACTTCC[C/G]GGATGAAGCAGTGCT | 84669 |
rs771195825 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60382272 | TGATCCCAGTGCTTT[C/G]GGAGGCTGAGGCTTG | 84669 |
rs771197758 | snp | C/T | 0.000867121 | 0.020804 | intron-variant | USP32 | GRCh38.p7 | 17:60255289 | TCATGTTAGGAACAT[C/T]TTTTTTTTCTTTTTT | 84669 |
rs771208613 | snp | C/T | 1.64969e-05 | 0.00287196 | missense | USP32 | GRCh38.p7 | 17:60192847 | AGGTCACTTTACCTA[C/T]ACCATGGGCACCAAG | 84669 |
rs771210696 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306933 | GTAATCCAAGTTAAA[A/T]TAGCTACAAAGAATA | 84669 |
rs771249137 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60337165 | AAACCTAGACTATCT[A/G]GTAAATATGCAGGCC | 84669 |
rs771272142 | in-del | -/TTT | | | intron-variant | USP32 | GRCh38.p7 | 17:60245187 | TATATTTATACTGTC[-/TTT]TATTATTACCTATGT | 84669 |
rs771272902 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60319309 | ACAGGGACTCAGATT[A/G]AGAATATTCAGATAA | 84669 |
rs771284593 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308631 | TGGATAACTATACGC[A/G]GAAAAATAAAACTAG | 84669 |
rs771289456 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60228338 | CAAAATCCTGTAGAC[-/A]AGACAGTAGAACCAA | 84669 |
rs771319522 | snp | A/T | | | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60424185 | CCACCCCCATGACCC[A/T]AACACCTCCCATCAG | 84669 |
rs771322949 | snp | C/T | 1.67618e-05 | 0.00289493 | intron-variant | USP32 | GRCh38.p7 | 17:60214574 | CTATTTAAAATTAAA[C/T]AAATACCAACAATCA | 84669 |
rs771323996 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60337036 | CTAGAGTTGTCAAGA[A/T]AGTTGTTAGCCCTTA | 84669 |
rs771325899 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60317786 | TGGGCAACACAGTGA[A/G]ACCAGCCTGGCCAAA | 84669 |
rs771333856 | snp | C/T | 1.74824e-05 | 0.0029565 | intron-variant | USP32 | GRCh38.p7 | 17:60185428 | CTTTTATGCCAGATT[C/T]CTGCTCTCTCAGAGG | 84669 |
rs771339612 | snp | C/T | 1.67536e-05 | 0.00289423 | intron-variant | USP32 | GRCh38.p7 | 17:60294643 | TAAGAGTTAATACTT[C/T]GTCAATGAAAAGGGA | 84669 |
rs771383704 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | USP32 | GRCh38.p7 | 17:60181464 | CATAAAGGAATCCAT[G/T]GGCCAAAGCTACCTC | 84669 |
rs771384029 | in-del | -/AAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60261063 | TGAACAGTCACGACT[-/AAA]ATTCCAGGACAGAAA | 84669 |
rs771411207 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60182247 | TAGCCCCTTTTATAC[C/T]TTTAAAAATTATTGA | 84669 |
rs771412702 | snp | C/T | 3.29457e-05 | 0.00405854 | missense | USP32 | GRCh38.p7 | 17:60226125 | ACGTAACTGAGGCTG[C/T]TTCCAATTCTATCTT | 84669 |
rs771429182 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258052 | AAAAAAGGGAGCAAG[C/G]AGATAAGATGAAGAA | 84669 |
rs771432231 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60320911 | CTACAACCCTCTCCA[A/G]AGTAGCTATGGTCCT | 84669 |
rs771439346 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60303736 | AAGTCACAGAAAGAA[A/G]GAAAAACCCAATATA | 84669 |
rs771454104 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328395 | TGAAGAGAAAAGCTA[C/G]CCCTTCTGCTGAGAG | 84669 |
rs771473422 | snp | C/T | 1.65007e-05 | 0.00287229 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181570 | ACATATCTGCCCAGC[C/T]CCATTTTCTTTGCTG | 84669 |
rs771478191 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, LOC105371850 | GRCh38.p7 | 17:60418249 | AGGCGTGAGACCCCT[C/T]GCCTGGCTAATTTTT | 84669 |
rs771488507 | snp | C/T | 1.72821e-05 | 0.00293951 | intron-variant | USP32 | GRCh38.p7 | 17:60269566 | AACAAACCTGTAAAA[C/T]AGGAAGAGATGCCAT | 84669 |
rs771489455 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60253630 | AATTAGCTGGGGGTG[A/G]TGGCACACGCCTGTA | 84669 |
rs771492040 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60276637 | AGTACTTCTGATTAA[C/T]TGGTGTTTACATAAT | 84669 |
rs771505454 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60345762 | CAAGGCAGGCGGATC[A/G]CTTAAGGCCAGGAGT | 84669 |
rs771509605 | in-del | -/AAAC | | | intron-variant | USP32 | GRCh38.p7 | 17:60332790 | TATGAATGTAATCTT[-/AAAC]ATGCATGCTATTTTT | 84669 |
rs771520585 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60249582 | CATTTATTCCTGCTC[C/T]CCTTCAAATCATGAA | 84669 |
rs771521956 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393069 | CACGTCCCATTTCCC[A/G]CCGTTTTTCATCTTG | 84669 |
rs771528616 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60347979 | TACAAAAAATTAGCC[A/T]GGCCTGGTGGCGGGC | 84669 |
rs771531220 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312497 | GTGGCATAACCACAG[C/T]TCATCGCAGCCTTGA | 84669 |
rs771554692 | in-del | -/AGA | 1.74488e-05 | 0.00295366 | intron-variant | USP32 | GRCh38.p7 | 17:60208871 | CTCAAAATCCAAAAG[-/AGA]AGAAGCATTTCTATA | 84669 |
rs771577414 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60391314 | TCTTATCAAAGTCAG[A/C]CGCTCAAACGGTGAA | 84669 |
rs771579167 | snp | A/C | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60406957 | AGGGACCAGATTAAC[A/C]CTTCTGCCATACACA | 84669 |
rs771610418 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265314 | AGTACTTGGTAGGGA[C/G]GATGCCAAAGAGATT | 84669 |
rs771613492 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon | USP32 | GRCh38.p7 | 17:60183292 | AATCCTGGGCTCAGA[C/G]AGCTCATCCCCCTGG | 84669 |
rs771616912 | snp | C/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416400 | GCGTATGCCATCAAA[C/G]AGCATGCCAACCTGC | 84669 |
rs771638023 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60302179 | TTGCTCCTGTCGCCC[A/G]GGCTGGAGTGCAATG | 84669 |
rs771658175 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60340004 | ATGTTAAAATACTGC[C/T]ATGATATCTCAAAAC | 84669 |
rs771706075 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194105 | TGGAGTGCAGTGGCG[C/T]AATTATGGCTCACAG | 84669 |
rs771711336 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60326590 | AGGCATGAGCCACTG[C/T]GCCCGGCCATGGTTT | 84669 |
rs771715009 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60251525 | AAAAAGTCAAATGAC[A/C]GTACCTATTGAGAGT | 84669 |
rs771723197 | snp | A/C | | | intron-variant, nc-transcript-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60402811 | AGTGGCCTGAAAGCT[A/C]GGGACTGGAATCCTC | 84669 |
rs771723463 | in-del | -/ATTTG | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60420093 | ATTTTATTTTATTTT[-/ATTTG]TTTTGTTTTATTTTA | 84669 |
rs771726795 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60359167 | CTAATTGCTTCCATG[C/T]CCCACCACCTAAAAT | 84669 |
rs771732802 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60378695 | GAAAGGTCAAATATT[A/G]TACGATTCTATTTAC | 84669 |
rs771740768 | in-del | -/AC | | | intron-variant | USP32 | GRCh38.p7 | 17:60260714 | GATAGAAAATTATAT[-/AC]ACAGATTTAGGAAAA | 84669 |
rs771805723 | snp | C/T | 3.35464e-05 | 0.00409537 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391946 | GGCACCCATGCTCCC[C/T]TCATCCCCTCGGCGG | 84669 |
rs771823950 | in-del | -/TT | | | intron-variant | USP32 | GRCh38.p7 | 17:60347352 | ACCACACCTGGCTCA[-/TT]TTTTTTTTTTTTTTT | 84669 |
rs771826167 | snp | C/T | 3.31214e-05 | 0.00406935 | intron-variant | USP32 | GRCh38.p7 | 17:60223406 | TTAGATGTAAAATTA[C/T]TTACCTTTACTGGTT | 84669 |
rs771827126 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60368992 | TTATTTTTTAAAAGA[-/T]TTTTTTTTTTTTTTT | 84669 |
rs771835373 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60388231 | TAGAAGAAATTCACC[C/T]ACTGTATTTTATTAC | 84669 |
rs771849065 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295411 | ATAGTACAGTAGTAC[A/C]CCCTTATCCATGGTT | 84669 |
rs771852787 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60258627 | TAAGTACCTTTCCTA[C/T]ATTTTCTTTTCCTTT | 84669 |
rs771874246 | snp | C/T | 1.67351e-05 | 0.00289263 | intron-variant | USP32 | GRCh38.p7 | 17:60211361 | TTAAGAGGCCAGTGA[C/T]TCCAGAAAGATTACC | 84669 |
rs771901687 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60324972 | CATGCCATTGCACCC[C/T]AGTCTGGGCAACAAG | 84669 |
rs771924763 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60325948 | ATTGGACTTTAGCCT[C/G]GGTGACAGAGTAAGA | 84669 |
rs771948350 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60187252 | AAGGCTGGATTTGAT[C/T]GTGCAATTAAGGTTC | 84669 |
rs771951145 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60276235 | TTGTAATAAAATAAA[A/G]AATGTAAAACTCATA | 84669 |
rs771958349 | snp | C/T | 1.67144e-05 | 0.00289084 | missense | USP32 | GRCh38.p7 | 17:60183183 | TCGGGCTGCTGATGA[C/T]GTTAGCGCTGAGTGA | 84669 |
rs771961356 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60236966 | CACTGTATGTATATA[C/T]TACATTTTGTTTATC | 84669 |
rs771964049 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60311886 | TTAGAAACAGTTGTA[C/G]CATGTTTCAACTGCT | 84669 |
rs771966018 | snp | A/G | 1.70455e-05 | 0.00291933 | intron-variant | USP32 | GRCh38.p7 | 17:60211519 | TTCTGTGGGAACTGG[A/G]ACAAACAATATGAGA | 84669 |
rs771970296 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60233918 | GATACTCCTCTCCTC[A/C]CAGGTTTATTGTAAC | 84669 |
rs771973087 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60370639 | GGGCATGGTGGTGCC[C/T]ACCCAACCACTCAGG | 84669 |
rs771973501 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416324 | GACATACAACAAGAA[C/T]TTCGTGAGTTCCATC | 84669 |
rs771979068 | snp | C/T | 1.66969e-05 | 0.00288932 | missense | USP32 | GRCh38.p7 | 17:60214685 | TTTGAGATAGATATT[C/T]GTGAATTTCCTTGAT | 84669 |
rs771990449 | snp | A/T | 1.76098e-05 | 0.00296725 | intron-variant | USP32 | GRCh38.p7 | 17:60181289 | GTGAACAAAACACAG[A/T]CCACTCTCTGAAAAC | 84669 |
rs771991664 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60372066 | AGGGAGAGGGGAAGG[A/G]GAAGTGGCTAAGGTG | 84669 |
rs772016924 | snp | A/C | 5.05089e-05 | 0.00502513 | intron-variant, splice-donor-variant | USP32 | GRCh38.p7 | 17:60219627 | TGCATTCTTAAGTTA[A/C]CTCTCGGTAAATGCT | 84669 |
rs772043257 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328057 | CTCCTGGGCAGAAGG[C/G]GGCAGGTCCCCACTG | 84669 |
rs772053906 | snp | C/T | 4.97748e-05 | 0.00498848 | missense | USP32 | GRCh38.p7 | 17:60205490 | CCTGTAAAGGGGCTG[C/T]CAGGAAGAGATGGCA | 84669 |
rs772056878 | snp | C/T | 6.20444e-05 | 0.00556941 | intron-variant | USP32 | GRCh38.p7 | 17:60207167 | ATGAGAAGGGGGAGA[C/T]GTTTCAGATAAAATG | 84669 |
rs772068141 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60189539 | AGATTCTTAATGTCT[C/T]TACCATTCAAATAAT | 84669 |
rs772068571 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60302003 | CAGTACTCCATAAAT[C/T]ACATAAGATATTTAA | 84669 |
rs772105733 | snp | A/T | 5.33234e-05 | 0.00516322 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231627 | AACAGGGACCCCCCA[A/T]AGCCCATGGGAGAGA | 84669 |
rs772108561 | snp | A/G | 1.65168e-05 | 0.00287369 | intron-variant | USP32 | GRCh38.p7 | 17:60214809 | AGTAAGAAAAAAGGC[A/G]GATGTGAAAAAGAAG | 84669 |
rs772138310 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407147 | ATGTGGCAATCTCAC[C/T]GAGGACGCACAGATT | 84669 |
rs772158077 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60188535 | TCCCATAAATGTTAG[C/G]AAAAACTCCTGGTAA | 84669 |
rs772163692 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233033 | GTTCATATGTGAAAA[C/G]TGAGGTAGAGCAAGA | 84669 |
rs772168961 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60333184 | TGGACTCCAGAAAAG[C/T]TTTACTAATAGCCTG | 84669 |
rs772171875 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60384235 | GATCCTTTTCATAAT[A/G]TAATCTCTCCAGACC | 84669 |
rs772184848 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60286670 | TAAGCCAGAAAGTAA[C/T]AGTAGCCTAAAAGAA | 84669 |
rs772196036 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60338142 | CAGCCTGGGCAACAT[A/G]GCGAAACTGCATCTC | 84669 |
rs772210856 | in-del | -/GTG | | | intron-variant | USP32 | GRCh38.p7 | 17:60385407 | GACGCGCATGACAGT[-/GTG]GTGGCACACGCCTGT | 84669 |
rs772214320 | in-del | -/GTAT/TA | | | intron-variant | USP32 | GRCh38.p7 | 17:60291572 | TGTGTGTGTGTGTGT[-/GTAT/TA]ATAAACACAAAAACA | 84669 |
rs772216745 | snp | A/C | 1.65496e-05 | 0.00287655 | intron-variant | USP32 | GRCh38.p7 | 17:60214598 | ACAATCAGACTCTCT[A/C]TGACTCTGAGATGCC | 84669 |
rs772228447 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60216903 | ACATTTTAGGATTAG[-/T]TGTAAGATTACAGCA | 84669 |
rs772291147 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60273090 | AGATTCTTGTGTTTC[A/G]GCTTCCCAAGTAGCT | 84669 |
rs772330734 | snp | A/G | 1.65866e-05 | 0.00287976 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181606 | CAAGTTCTCTTTACT[A/G]CTTGACAGTTTATTT | 84669 |
rs772342602 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60293581 | AGCACCATAACCACC[A/G]CCAAAAACTGCATGC | 84669 |
rs772351398 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60255400 | CCTCCTGGGTGCAAG[C/T]GATTCTCCTGCCTCA | 84669 |
rs772377523 | snp | A/G | 1.65299e-05 | 0.00287483 | missense | USP32 | GRCh38.p7 | 17:60185618 | CGGCTTGCGCTCGCC[A/G]ACTCTGCTCCACACT | 84669 |
rs772388467 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308704 | AGGCTGAGGCAAGTG[A/G]ATCACTTGAGGTCAG | 84669 |
rs772410623 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295203 | CGTACAAAATACAAG[A/G]TGTTCACTGAAATAC | 84669 |
rs772411170 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60186132 | TATTCACAAATGTTA[C/T]ATCGGTAACATTCTG | 84669 |
rs772419182 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60280724 | CCCTATTTTTATCAC[-/AA]GTTTCCACATTCCTA | 84669 |
rs772422001 | snp | C/T | 1.98924e-05 | 0.0031537 | intron-variant | USP32 | GRCh38.p7 | 17:60252363 | ATTTCAACTATATAA[C/T]TGAAACTACAAATTT | 84669 |
rs772444484 | in-del | -/TC | 0.00276575 | 0.0370841 | intron-variant | USP32 | GRCh38.p7 | 17:60255297 | GGAACATCTTTTTTT[-/TC]TTTTTTTTTTTTTTT | 84669 |
rs772453540 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60408513 | CTCCCAAGTAGCTGG[A/G]ATTATAGGTGCATGC | 84669 |
rs772456072 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60348411 | GGAGAAAAGAAGGAG[A/C]AGTAGAAGAGTATGC | 84669 |
rs772469472 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | USP32 | GRCh38.p7 | 17:60180607 | TGGCATAAGTGACGT[A/G]ATGGCCCCCACCCAG | 84669 |
rs772473142 | snp | A/G | 1.6486e-05 | 0.00287102 | missense | USP32 | GRCh38.p7 | 17:60190573 | CTTACCCTTTCCTGG[A/G]ATGTTTGATAGCGAA | 84669 |
rs772500052 | snp | C/T | 8.53439e-05 | 0.00653182 | intron-variant | USP32 | GRCh38.p7 | 17:60252473 | GTAAATCAAAGTTTA[C/T]TAACTGCATAATATT | 84669 |
rs772520294 | snp | C/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404091 | AAAGAAATATGCGCA[C/G]ACACACATATTTCTG | 84669 |
rs772544862 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60241523 | CAGAGTTGAAATGGG[C/T]AGTTTGTTCTTTATT | 84669 |
rs772550525 | snp | C/T | 1.64852e-05 | 0.00287094 | missense | USP32 | GRCh38.p7 | 17:60211033 | GCTTTAATGGGGCAA[C/T]ATTCTTCTGAGTTCC | 84669 |
rs772562037 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60331327 | TCCCAGCACTTTGGG[A/G]GGCCAAGGCAGGCGG | 84669 |
rs772569432 | snp | C/G | 1.64738e-05 | 0.00286995 | missense | USP32 | GRCh38.p7 | 17:60198330 | ATACTTGAATCCAAA[C/G]CGCATCATATAGGTC | 84669 |
rs772586065 | snp | C/T | 1.73993e-05 | 0.00294947 | missense | USP32 | GRCh38.p7 | 17:60181704 | GGCTGCTGTTTTTGC[C/T]GGAGGGACAGCTGGT | 84669 |
rs772605028 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60178561 | CTGGGTCTCCCACAA[A/G]GCTCTGGGTGGAAGG | 84669 |
rs772613018 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60329393 | GCTAGGTATGAGCCC[A/G]GACCATAAAATGTTT | 84669 |
rs772632812 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60240642 | AGTCTAGAAGCTCAG[C/T]CAGAGGTGAAAGTTT | 84669 |
rs772637225 | in-del | -/C | 7.10581e-05 | 0.0059602 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231619 | TAAGGAGAACAGGGA[-/C]CCCCCCAAAGCCCAT | 84669 |
rs772641150 | in-del | -/CTG | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60403018 | GGGTAAGCCGTATCT[-/CTG]TTTTTTTTTTGAGAC | 84669 |
rs772642882 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60377188 | AGTTTGGGCCAGGCA[C/T]GTGGTTCACGTCTGT | 84669 |
rs772666113 | snp | C/G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60190324 | AAGTTACCAGCCTCA[C/G/T]GTACTCTGTTATAGC | 84669 |
rs772669752 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60242590 | TAATTTTTGTGTTTT[C/T]AGTAGAGATAGGGTT | 84669 |
rs772671220 | snp | A/T | 1.66114e-05 | 0.00288192 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60294776 | AACATAGTTCCCAGA[A/T]TCACTTGAAAAAAGA | 84669 |
rs772700568 | snp | C/G | 7.38362e-05 | 0.00607558 | intron-variant | USP32 | GRCh38.p7 | 17:60207001 | AGCAATCATGAGAAG[C/G]AGTTCTAGTTCTATC | 84669 |
rs772711891 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60263378 | CAGATGAATTAGATA[A/C]AACAGAGAAGAGTTG | 84669 |
rs772716940 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60221345 | TTATTTTTCATAAAC[A/G]TAATTATTAAGAACT | 84669 |
rs772719995 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414728 | GCCACCACGCCCAGC[C/T]AGTTATTGTTTTAAA | 84669 |
rs772720742 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60372986 | CCTGGCTAACATAGC[A/G]AGGTCTCTACAAAAC | 84669 |
rs772737137 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60224817 | AACAATAGGGTAAGA[C/T]TGAGGGTTCTGCTAC | 84669 |
rs772741011 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60226633 | TATAGAAAACATGAA[G/T]AAAATATCACATGTA | 84669 |
rs772743216 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412609 | TCTAAGGCAAGGTGA[C/T]TTTTCTGTCTGAAAA | 84669 |
rs772747312 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312499 | GGCATAACCACAGCT[C/T]ATCGCAGCCTTGACC | 84669 |
rs772755160 | snp | C/T | 4.98434e-05 | 0.00499192 | intron-variant | USP32 | GRCh38.p7 | 17:60294672 | GATAAAATGTAAATC[C/T]TTAACTATACCTCTG | 84669 |
rs772768984 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373878 | TCTTTATTTAAAAAG[G/T]TTTTACTATTCATGT | 84669 |
rs772772422 | in-del | -/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393487 | GATTTTCAACTCTTA[-/T]TTAGTTTGCGTCTTC | 84669 |
rs772804226 | snp | C/T | 3.32768e-05 | 0.00407888 | intron-variant | USP32 | GRCh38.p7 | 17:60198251 | TTTAGATGGATCCCC[C/T]GAACTCACCAATCCT | 84669 |
rs772814237 | snp | C/G | 1.71372e-05 | 0.00292717 | intron-variant | USP32 | GRCh38.p7 | 17:60391843 | AGGCTGCCCGTCGCG[C/G]GCCTCCCAGGCAGCT | 84669 |
rs772820367 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60312311 | GAGTAAACTCTAGTA[C/T]ACCAATCTAACTGCT | 84669 |
rs772826389 | snp | A/G | 6.60175e-05 | 0.00574494 | missense | USP32 | GRCh38.p7 | 17:60183381 | GATCAAAACTTTCCC[A/G]AGGAAATTTGACAAT | 84669 |
rs772827233 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60240146 | CCAATGTCTGTGCTT[A/C]CTCAAAGAGAATTTC | 84669 |
rs772843661 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60390950 | ATTCCGGCCATAAAC[A/T]GTGCAACAAGACACT | 84669 |
rs772860070 | snp | C/T | 6.72156e-05 | 0.00579683 | missense | USP32 | GRCh38.p7 | 17:60219765 | TCCAGCTCTGGGATG[C/T]CTGTCTTGCTGTTCT | 84669 |
rs772862300 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191071 | TGTAACACCTAGCTC[C/T]TTGTCTGTAAAATGG | 84669 |
rs772869341 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416391 | ATGAAACAGGCGTAT[A/G]CCATCAAAGAGCATG | 84669 |
rs772878813 | snp | C/T | 1.64795e-05 | 0.00287045 | intron-variant | USP32 | GRCh38.p7 | 17:60236244 | TCTAACCATCCTCTG[C/T]ATGTACAAAAGAAAT | 84669 |
rs772884901 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60354829 | GGCAGGCAGATCGCT[C/T]AAGGTCAGGAGTTCG | 84669 |
rs772890083 | snp | C/T | 1.68858e-05 | 0.00290561 | missense | USP32 | GRCh38.p7 | 17:60181632 | TATTTTTGCTGCCAA[C/T]CTGGGGCAGCCGGAG | 84669 |
rs772892066 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | USP32 | GRCh38.p7 | 17:60198338 | ATCCAAACCGCATCA[C/T]ATAGGTCTTTCTTCC | 84669 |
rs772892746 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60247152 | CGTCTAGTAGTTTAG[A/G]TCTTAGATTTAAGTC | 84669 |
rs772893850 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60287060 | GAGGCTGAGGCAGAA[A/G]AATCGCTTGAACCTG | 84669 |
rs772913682 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392617 | TTCTGAGGGATGCGG[C/T]ATATGGCTCAGAAGA | 84669 |
rs772919136 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | USP32 | GRCh38.p7 | 17:60345579 | TCCTCTTGAAAGCAT[C/T]CTTCAGTCGTTTTAG | 84669 |
rs772922893 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191825 | ATGCCTACTTTAGAC[C/T]CAGTTTGCTAAGTCT | 84669 |
rs772926400 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60258399 | GATCAAGAAGAAAGG[A/G]AAGGTCTTTTAAACT | 84669 |
rs772948546 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60399867 | GCAAGTGTGCCTGCA[A/G]CAGTGAGAGAAGGGG | 84669 |
rs772965288 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60299548 | TCATTCATGGGTGTG[C/G]ACCCCTCATGATCTA | 84669 |
rs772977813 | snp | C/T | 1.65427e-05 | 0.00287595 | missense | USP32 | GRCh38.p7 | 17:60214627 | CCTCTTACCTCACTG[C/T]TGTATAGCCACAGGC | 84669 |
rs772982795 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60271244 | ATTAAACCTGCAAAC[-/AT]ATGAGAAGATGGTTT | 84669 |
rs772983327 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60323199 | GTATACAAATGTTCA[C/T]AGCAGCATTATTTAT | 84669 |
rs772986860 | snp | C/T | 1.77087e-05 | 0.00297557 | missense | USP32 | GRCh38.p7 | 17:60181727 | CAGCTGGTTCCACTT[C/T]TTCTTGATGAAGAAG | 84669 |
rs772988036 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60338497 | GCAATTTGGGAAGTC[A/G]AGGCAGGGTGATCAC | 84669 |
rs773040640 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409620 | ATAGAAAAAGTATGA[C/T]AGTGAAAAAAAGTCT | 84669 |
rs773046726 | snp | C/G | 3.59822e-05 | 0.00424144 | intron-variant | USP32 | GRCh38.p7 | 17:60226274 | AGCAAAGTTTATAAT[C/G]TGACAACTATGTAGT | 84669 |
rs773058051 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60313408 | GTTTCTTTTCTTCAA[A/T]TGTGTTTCATAATAC | 84669 |
rs773072431 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233253 | GGAGAATCGCTTGAG[C/T]CCAGGAGTTCGAGAC | 84669 |
rs773084741 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60384963 | AAAATACAAAAATTA[G/T]CCAGGTGTTGTCAGG | 84669 |
rs773096221 | snp | C/T | 1.75588e-05 | 0.00296295 | intron-variant | USP32 | GRCh38.p7 | 17:60185419 | GTCTTCTTTCTTTTA[C/T]GCCAGATTCCTGCTC | 84669 |
rs773108589 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60255548 | CGTGATCCATCCGCC[C/T]TGGCCTCCCAAAGTG | 84669 |
rs773112065 | in-del | -/C | 8.31705e-05 | 0.00644812 | intron-variant | USP32 | GRCh38.p7 | 17:60255301 | ATCTTTTTTTTCTTT[-/C]TTTTTTTTTTTTTTG | 84669 |
rs773117367 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60291931 | TTGAAAATTTAAGCA[-/T]TCCACTCTTCCTATC | 84669 |
rs773122176 | snp | C/T | 0.000201511 | 0.0100357 | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422237 | GGAAAATGAGTTCAA[C/T]AGCCTTACCAGGTGG | 84669 |
rs773130989 | snp | A/G | 1.67058e-05 | 0.00289009 | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60266120 | ACTCTTATGGAGGAA[A/G]ATCATTTTTGTATTC | 84669 |
rs773154330 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60301913 | GACTACTGTAAAATA[C/T]GTACAGATGGTCCTC | 84669 |
rs773156737 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392424 | GCAGCCGCGCGCCCC[A/G]CCCGGGCGCCTCCGC | 84669 |
rs773163402 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60308861 | CTAAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 84669 |
rs773187833 | snp | A/G | 4.94189e-05 | 0.00497062 | missense, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179364 | AATTGTGCATAGTCT[A/G]TCCCCTGCTGCTCAT | 84669 |
rs773195598 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60220453 | CACATATGTTTTGTC[C/T]ATGACTTAAACAAAA | 84669 |
rs773198581 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60272420 | ACCATTTTATCTGTG[C/T]TTGTTTTTCCTCCAA | 84669 |
rs773201488 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60295608 | GTTGTCCAGTGTATC[C/T]ACATGCTACTCGCCT | 84669 |
rs773208853 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60395933 | CTAATTTATGTATAA[C/G]TTCATTGCTACAACG | 84669 |
rs773209116 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60229388 | ATCTCACTACATATG[C/T]AGCCAGAATTAATAA | 84669 |
rs773210780 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60244718 | CTTACTGCAACCTCT[A/G]CCTCCTGGGTTCAAG | 84669 |
rs773217073 | snp | C/T | 4.94197e-05 | 0.00497066 | missense | USP32 | GRCh38.p7 | 17:60181461 | GCTCATAAAGGAATC[C/T]ATTGGCCAAAGCTAC | 84669 |
rs773218700 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60321181 | CTCCCAGCTGTATAT[G/T]AATGGATATAAGCCT | 84669 |
rs773223858 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60323738 | TAAGGCTTTTTATAT[C/G]TCACCTAAAATTTCT | 84669 |
rs773245430 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412633 | CTGAAAAACTCTAAT[A/G]TTAGTCCCCAGTCTC | 84669 |
rs773250013 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60263108 | CATGTGCTACTGTGC[C/T]TGGCTACGTTTTTTC | 84669 |
rs773265122 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60199071 | CAGTGAGCTGTGATC[A/G]TGCCACTGCACTCCA | 84669 |
rs773290176 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60194366 | CTTTGTATTCTCATA[C/T]GTTCCAGAACCTGGA | 84669 |
rs773300994 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60243342 | TTTACAATCTTGATG[C/G]CTTTTATTTCCTTTT | 84669 |
rs773310240 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60287987 | GGCATGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 84669 |
rs773356180 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60282949 | TATTCCCAAGGGGCT[C/T]GCAACTTGTGGGGGT | 84669 |
rs773394907 | snp | C/G | 1.6489e-05 | 0.00287128 | missense | USP32 | GRCh38.p7 | 17:60205544 | GTGAAGTTCTTCTCA[C/G]TTCCACATGGCACAA | 84669 |
rs773409588 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60230126 | ACCACAAATTACTTT[A/C]TAAAAAATTTGTAGT | 84669 |
rs773423418 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60333213 | TGACAATCACAAGCC[C/T]TACCAAAAACATAAA | 84669 |
rs773424755 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60352653 | GCACATTGGTGTCGA[C/T]GCAATAAACAAGACT | 84669 |
rs773444256 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60317433 | AGCTGGGAGGATTAC[C/T]TGAGCCAAGGAGGTC | 84669 |
rs773444568 | snp | A/G | 1.65244e-05 | 0.00287436 | synonymous-codon | USP32 | GRCh38.p7 | 17:60301660 | AACTATTAAATTATT[A/G]AAGTGCAGCCCTTTG | 84669 |
rs773454602 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60302279 | AGCTGGGATTACAGG[C/T]CACTTGGGATTACAT | 84669 |
rs773477618 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60351246 | CCAATCTACCACCTA[C/T]CCAAACCCCCATCAC | 84669 |
rs773478007 | snp | A/G | 1.65677e-05 | 0.00287812 | intron-variant | USP32 | GRCh38.p7 | 17:60212121 | GACAGATAGGAATGT[A/G]TTAATTTCTTATCTA | 84669 |
rs773500288 | snp | C/T | 1.64868e-05 | 0.00287109 | synonymous-codon | USP32 | GRCh38.p7 | 17:60223477 | CTGAGGGTTAAGGTG[C/T]AACAAAATATTCCCA | 84669 |
rs773508532 | in-del | -/AT | | | intron-variant | USP32 | GRCh38.p7 | 17:60371771 | AAGTAAAAAGGCCAC[-/AT]GAGACATTAGAAGAA | 84669 |
rs773519967 | in-del | -/TAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60260765 | TAATCGCTTATACAG[-/TAT]TATTCAATTTTTAAA | 84669 |
rs773542857 | snp | C/T | 1.64879e-05 | 0.00287118 | intron-variant | USP32 | GRCh38.p7 | 17:60236118 | TGTGAAAAATGTAAA[C/T]AGACAGGAATCTAAC | 84669 |
rs773545599 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60277295 | AACAACTCTTTAATG[C/T]CAGAAGTCAATCCTC | 84669 |
rs773566432 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60237449 | TGAGGTGAAAATGGC[A/G]TAATATGAAATTATT | 84669 |
rs773567488 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | USP32 | GRCh38.p7 | 17:60205612 | GGGTAGGTCCCCATT[A/G]GTAGTTAGGGTGAAC | 84669 |
rs773574606 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | USP32, CA4 | GRCh38.p7 | 17:60178927 | GATTATGGTAAACTC[A/T]ATACTCACTACATAT | 84669 |
rs773582870 | snp | A/C | 1.7339e-05 | 0.00294435 | missense | USP32 | GRCh38.p7 | 17:60208203 | GGTAGTACCATCTAA[A/C]TTAATCACTAGTAAA | 84669 |
rs773586367 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60239085 | TAATTTTTGAGGAAA[C/T]AGTTTTGTTAGATAT | 84669 |
rs773600784 | in-del | -/AGAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60321673 | TTTAAACATAGTAAC[-/AGAA]AGAAAATACAGAAGA | 84669 |
rs773600906 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60344624 | TCTGCTAATTTTTTT[C/G]GTTGCTGTTTTTAAG | 84669 |
rs773612394 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | USP32 | GRCh38.p7 | 17:60190622 | CCCAATCCACAGCGA[C/T]ATAGGCATTTCCAAT | 84669 |
rs773613730 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60342636 | GCCTCAGCAATGGTG[C/G]ATGCCCCTCCCTCAG | 84669 |
rs773630348 | snp | A/G | 1.64914e-05 | 0.00287149 | missense, utr-variant-5-prime | USP32 | GRCh38.p7 | 17:60271422 | CAAATCGTCCAGTCC[A/G]GGATTGAGCCTTCAA | 84669 |
rs773643296 | in-del | -/AA | | | intron-variant | USP32 | GRCh38.p7 | 17:60386367 | TAGTTCATAAATTAA[-/AA]AAAAAAAAAAAAAAA | 84669 |
rs773643947 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60368827 | CAAACATTTCCCAAA[A/C]AACCAAACCAAAACA | 84669 |
rs773647412 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404775 | AGAAACAACCTTCTC[A/G]TCTTTCCTGTATGAA | 84669 |
rs773655428 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60253537 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACTTGAG | 84669 |
rs773657814 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60240926 | CTGGGTAAATTCTGA[C/G]TTAAGTATAACATAG | 84669 |
rs773664615 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60195595 | CTCCCACCTTGGCCT[C/T]CCGAAGTGCTGGGAT | 84669 |
rs773667021 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60361508 | GCCTCCTTAGATACA[C/T]ACAGAGAGTGCTTCT | 84669 |
rs773680840 | snp | A/C | 3.3024e-05 | 0.00406336 | intron-variant | USP32 | GRCh38.p7 | 17:60198482 | AGAGAGTTCAGAAGA[A/C]AGGCCTCTGATTCCT | 84669 |
rs773701904 | snp | C/T | 0.00013214 | 0.00812726 | intron-variant | USP32 | GRCh38.p7 | 17:60192838 | TTCTTTTGCAGGTCA[C/T]TTTACCTATACCATG | 84669 |
rs773703910 | snp | A/G/T | 3.30804e-05 | 0.00406686 | missense | USP32 | GRCh38.p7 | 17:60181349 | TATAGATTATAAATA[A/G/T]GCTTAATACGAGTAT | 84669 |
rs773743582 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60270161 | GGTTTTCAAACATTT[C/T]GTAAAAAAAAGAAAT | 84669 |
rs773747237 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60290885 | GATGTCTAGGGGTCA[C/G]TTTTGTGGAACTAAT | 84669 |
rs773774214 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | C17orf64, USP32 | GRCh38.p7 | 17:60421748 | CCGGACTCTGCCCAC[C/G]GCGTTTCCGCCCTCG | 84669 |
rs773779465 | snp | A/G | 0.000116788 | 0.00764071 | intron-variant, upstream-variant-2KB | C17orf64, USP32 | GRCh38.p7 | 17:60422664 | GTGGGGTGTGAGGGA[A/G]GGAGGGAAGGAGGGT | 84669 |
rs773784245 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60197177 | AAATTAAGAATCTGT[C/T]TCAAAAAAAAAAAAG | 84669 |
rs773785026 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60191171 | CTTTGGGAGGCCGAG[G/T]TGGGTGGATCACCTG | 84669 |
rs773805655 | snp | C/T | 1.65627e-05 | 0.00287769 | intron-variant | USP32 | GRCh38.p7 | 17:60226015 | AATAAACCAATAAAC[C/T]TCAGGGGAATAGGTC | 84669 |
rs773808261 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416328 | TACAACAAGAATTTC[A/G]TGAGTTCCATCACAT | 84669 |
rs773829505 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405640 | GTGGCATGTTGCCTA[C/T]AGTCCCAGCTGCTCA | 84669 |
rs773844063 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60249465 | TGTTGTTAGTCTGCT[C/G]CTTCCCCTAACCAGT | 84669 |
rs773851147 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60384485 | CCTGAATCTTATTCA[C/T]AAGATAGTGATGAGC | 84669 |
rs773854889 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60248309 | ACTTCTTCCTTTGTC[A/T]TTAGTTTTCAACACT | 84669 |
rs773859656 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60414936 | GCTAGCTGCAACCTA[C/T]GGTCTCCCGGGTTCA | 84669 |
rs773861108 | snp | C/T | 5.53756e-05 | 0.00526163 | intron-variant | USP32 | GRCh38.p7 | 17:60181756 | AGGAGAACCTGTGAA[C/T]AGGACAGAAGAAAAG | 84669 |
rs773883196 | snp | A/C | 1.76502e-05 | 0.00297066 | intron-variant | USP32 | GRCh38.p7 | 17:60208028 | TCTTTGGAGGATAGA[A/C]TCAAAAGTTTCTTAG | 84669 |
rs773887194 | snp | A/G | 1.70834e-05 | 0.00292257 | intron-variant | USP32 | GRCh38.p7 | 17:60391852 | GTCGCGGGCCTCCCA[A/G]GCAGCTCGCCCAGAC | 84669 |
rs773887761 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60315009 | TAAACAGGGCAAATG[A/C]CTTAAATAAAAAGAT | 84669 |
rs773961272 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60226498 | ATTCTGTTGGCAGCC[A/G]TTTTTTTAACATTAA | 84669 |
rs773973063 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP32, SCARNA20 | GRCh38.p7 | 17:60233278 | CGAGACTAGCCTGGC[A/C]GGCATAGTGAGACCC | 84669 |
rs773973643 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60301719 | CCTGGAAAAAGATGA[C/T]AAAGCCAACCTTAGG | 84669 |
rs773975700 | snp | C/T | 1.66846e-05 | 0.00288826 | missense, intron-variant | USP32 | GRCh38.p7 | 17:60391930 | CGATCCGTGACTCCT[C/T]GGCACCCATGCTCCC | 84669 |
rs773986598 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60301388 | TTTTTACTTTTAGCC[A/G]CTCTAGTAGGTGTGA | 84669 |
rs774026738 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | USP32 | GRCh38.p7 | 17:60222486 | GGACCATTTCATAGT[C/T]TCTTCCATGAATCAG | 84669 |
rs774038631 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60235368 | CAGAGACACCAAAGT[C/T]CGTGTTTCCCAATTA | 84669 |
rs774048163 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60233869 | CTTATTGAATAAATT[C/T]CCATACTCTGCCTCC | 84669 |
rs774051615 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60268986 | AAATTATGCTACAAC[-/A]ATTTTAGTTAGGTTA | 84669 |
rs774053073 | in-del | -/AAG | | | intron-variant | USP32 | GRCh38.p7 | 17:60385062 | ACTGAAGAATCACAA[-/AAG]AAGTGAAAATGGCAG | 84669 |
rs774075289 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60187182 | ATGGGTTTTCAGGTG[A/C]GACTTCTTCCCTATA | 84669 |
rs774079401 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60385896 | AGCCTTATGTTAATG[A/T]ATACTAAGTCCCTAA | 84669 |
rs774096210 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon | USP32 | GRCh38.p7 | 17:60209487 | AAAAGCCAGAAGTTC[C/T]TGGGAGTCCTGTTGC | 84669 |
rs774098713 | snp | A/T | 1.64836e-05 | 0.0028708 | synonymous-codon, intron-variant | USP32 | GRCh38.p7 | 17:60288584 | ATCATCAGTGAGGGT[A/T]ACATACACACCTCCA | 84669 |
rs774099955 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60323418 | AATAGTGAAATCTAT[A/G]TAGACAGAAAGTAGA | 84669 |
rs774133894 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60387073 | TTCATAGGAAGGCAA[A/G]TAAGTGCTTTAATAA | 84669 |
rs774142388 | in-del | -/AAT | | | intron-variant | USP32 | GRCh38.p7 | 17:60279837 | CCAGAGCCTGTCTCA[-/AAT]AATAATAATAATAAT | 84669 |
rs774143059 | snp | C/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409075 | TTTCTCAGCCGGGCA[C/G]AGTGGCTCATGCCTG | 84669 |
rs774186115 | snp | A/G | 0.160858 | 0.233587 | synonymous-codon | USP32 | GRCh38.p7 | 17:60211055 | CTGAGTTCCACTCCA[A/G]AGTTCCTGCACTAAA | 84669 |
rs774206230 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60310576 | TGGTGGCACGCGCCT[A/G]TAGTCCCAGCTACTT | 84669 |
rs774220831 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60363517 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAATT | 84669 |
rs774224248 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60200994 | CCTCCCAAGTAGCTG[A/G]GACTACAGGTGTGTG | 84669 |
rs774227984 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60366891 | GCCAGGGTGCGATCT[C/T]GGCTCACTGCAAGCT | 84669 |
rs774232259 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60196872 | TTATTTAAGTAAAGA[C/T]TTATTTAAATCTTTA | 84669 |
rs774232341 | snp | C/G | | | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231616 | TGGCTAAGGAGAACA[C/G]GGACCCCCCAAAGCC | 84669 |
rs774244605 | snp | C/G | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60422079 | GAGGCCGCAGGGGCA[C/G]TGCTGGCTCACTGTG | 84669 |
rs774280636 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60396340 | CCTTAGTCTCCCAAA[A/G]TGCTGGGATTATAGG | 84669 |
rs774295396 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60289851 | AATAGACATGCTAAA[A/G]AATACGAATAATTAG | 84669 |
rs774302209 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60285331 | AAGGGCACTGAAAAG[C/T]AGTAGAATCAAGCTT | 84669 |
rs774305014 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60296117 | CCTTAGTTTTAATAT[A/T]TTTAAAAAATCAAAT | 84669 |
rs774311090 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60409089 | ACAGTGGCTCATGCC[C/T]GTAATCCCAGCACTT | 84669 |
rs774347956 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | USP32 | GRCh38.p7 | 17:60198354 | ATAGGTCTTTCTTCC[A/G]GGTATGCACAGTACA | 84669 |
rs774360678 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60357496 | TATGTAGACCAAGCA[A/G]GCAACAGAGCAAGAC | 84669 |
rs774370772 | snp | A/G | 5.32647e-05 | 0.00516038 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231569 | GGCAGTCCTGACGAC[A/G]ATCCTCGAGGGCTGC | 84669 |
rs774373761 | snp | C/T | 1.65307e-05 | 0.0028749 | intron-variant | USP32 | GRCh38.p7 | 17:60226025 | TAAACCTCAGGGGAA[C/T]AGGTCATATTTACCG | 84669 |
rs774380028 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60333142 | GGGGCACAACTCCCC[A/G]CAAGGTTGAAAATCT | 84669 |
rs774439302 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60230481 | ATTCTAATAACTTCT[C/T]AGAGATTGCAACATT | 84669 |
rs774458931 | snp | C/G | 1.83404e-05 | 0.00302818 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231480 | TAAATTCAGAGAAGA[C/G]AGGTGTTTCATTCCT | 84669 |
rs774493193 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60306347 | TTAAAATCCCTATAA[C/T]AATTTTCTGGCCGGG | 84669 |
rs774497179 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60270584 | ATCCCAGCACTTTGG[G/T]AGGCTGAGGTGGGCA | 84669 |
rs774511410 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60407041 | TGGCAGTGCAGAACT[A/G]ACGTCATTGAGATAA | 84669 |
rs774560359 | snp | A/G | 4.10534e-05 | 0.00453046 | intron-variant | USP32 | GRCh38.p7 | 17:60252354 | GTATGTGAAATTTCA[A/G]CTATATAATTGAAAC | 84669 |
rs774581922 | snp | C/T | 1.65348e-05 | 0.00287526 | missense, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265425 | ACCTTTGTGGTGTCA[C/T]GTGCATTCAGTATGC | 84669 |
rs774592089 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60364108 | TCAAAGTACCAGCAG[A/G]TTCAGTGTCTGGTGA | 84669 |
rs774608934 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60272011 | GCAGAGATGGGGTCT[C/T]GCTATGTTGGTCAGG | 84669 |
rs774618496 | snp | A/G | 2.85539e-05 | 0.00377838 | intron-variant | USP32 | GRCh38.p7 | 17:60206995 | TAAAGGAGCAATCAT[A/G]AGAAGGAGTTCTAGT | 84669 |
rs774620547 | snp | A/C | 3.31433e-05 | 0.0040707 | missense | USP32 | GRCh38.p7 | 17:60183400 | AAATTTGACAATTTT[A/C]TGTGATTTTATCCAC | 84669 |
rs774658113 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60193340 | AGAAAGCTGTATATT[G/T]AGAAGTCTTCTTTAA | 84669 |
rs774658790 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60347950 | GCACAATGAAACCCC[A/G]TCTCTACTAAAAATA | 84669 |
rs774660009 | snp | C/G | 1.75004e-05 | 0.00295802 | intron-variant | USP32 | GRCh38.p7 | 17:60223603 | TATAAAAAAAAAAGA[C/G]GATAGAATCTCTTAT | 84669 |
rs774668549 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60383999 | ATGGCAGTGGGGACT[A/C]AAGTGGAGGCAATTA | 84669 |
rs774681031 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60313733 | ATACTTATACTAAAG[G/T]CTATTCAAGACTCAC | 84669 |
rs774681984 | snp | C/T | 0.000103403 | 0.00718963 | intron-variant | USP32 | GRCh38.p7 | 17:60219815 | AAGATAAAAAGAGAT[C/T]ACTAAAAAAAGAAAC | 84669 |
rs774683920 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60253680 | TTGAGGCAGGAGAAT[C/T]GCTTGAACCTGAGAG | 84669 |
rs774690544 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60345856 | GCATGGTGGTGCATG[A/C]CTATAATCCCAGCTA | 84669 |
rs774695354 | in-del | -/A | | | upstream-variant-2KB, intron-variant | C17orf64, USP32 | GRCh38.p7 | 17:60419732 | GCGAGACACCATCTC[-/A]AAAAAAAAAAAAAAA | 84669 |
rs774706222 | snp | A/G | 1.68125e-05 | 0.00289931 | synonymous-codon | USP32 | GRCh38.p7 | 17:60185472 | TACCAGGATGGGTGG[A/G]AGCCTCCAGAGATCC | 84669 |
rs774717962 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60225034 | ATAGAATCTGATGTG[A/G]GGTGCATTTAATTTA | 84669 |
rs774726572 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60240715 | GGCATGTGCAAAGCC[G/T]TCTAAATTACCCAAT | 84669 |
rs774730299 | snp | A/G | 4.98807e-05 | 0.00499378 | intron-variant | USP32 | GRCh38.p7 | 17:60212136 | GTTAATTTCTTATCT[A/G]TCTAATTTATACCCA | 84669 |
rs774732320 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328438 | CAGGATACCCTGGCT[A/G]CAGAGAGGAGCTGCC | 84669 |
rs774733393 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181465 | ATAAAGGAATCCATT[A/G]GCCAAAGCTACCTCA | 84669 |
rs774743330 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60365278 | GAGGTTAGGAGTTAG[A/G]GACCAGCCTGGCCAA | 84669 |
rs774754544 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60298527 | AATAGTTGTTATAGT[A/G]TATTGTTTCTTATTT | 84669 |
rs774758623 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60400604 | ACATATTACATTTGA[A/G]ATGTCTATTAGACAT | 84669 |
rs774786091 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60391384 | GCATAGGCTCTGGGA[A/G]AAGGCAGGGACTCCC | 84669 |
rs774795135 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60292490 | CATCTCAGTTAGTGG[C/T]AATTCCATTCATTTA | 84669 |
rs774800137 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60240508 | GGAGAGAGAGAGAGA[A/G]AGAGACAAAAGACAG | 84669 |
rs774818947 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60262512 | GACTTATTTGTAAAT[A/G]TCCTCCGTTTAAATG | 84669 |
rs774820954 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60280446 | GAATACAAATAGCTC[C/T]ACAGTTTCCTTTGTG | 84669 |
rs774823380 | snp | C/T | 4.95569e-05 | 0.00497755 | missense | USP32 | GRCh38.p7 | 17:60181584 | CCCCATTTTCTTTGC[C/T]GGCATCCAAGTTCTC | 84669 |
rs774836186 | snp | A/G | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60405879 | TTATTATTTGGCTGG[A/G]TGCAGAAGCTCACTC | 84669 |
rs774852354 | snp | A/C | 1.64819e-05 | 0.00287066 | intron-variant | USP32 | GRCh38.p7 | 17:60236250 | CATCCTCTGTATGTA[A/C]AAAAGAAATTAAATA | 84669 |
rs774866093 | in-del | -/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60315319 | GCAGGAGAATGGCTT[-/G]AACCCGGAAGGCAGA | 84669 |
rs774880977 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60329383 | ACTATTATATGCTAG[A/G]TATGAGCCCAGACCA | 84669 |
rs774899602 | in-del | -/AG | 1.83586e-05 | 0.00302968 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231477 | TTGTAAATTCAGAGA[-/AG]AGAGGTGTTTCATTC | 84669 |
rs774909327 | in-del | -/TG | | | intron-variant | USP32 | GRCh38.p7 | 17:60291539 | CTCTGTGTGTGTATG[-/TG]TGTGTGTGTGTGTGT | 84669 |
rs774918188 | snp | A/G | 3.4528e-05 | 0.00415485 | intron-variant | USP32 | GRCh38.p7 | 17:60208238 | AAAGATCTTTTATTG[A/G]TAAAATGCAGGTTTC | 84669 |
rs774921022 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60236590 | AGCCTTATTGAGGAA[A/T]AATTTACATATATAT | 84669 |
rs774925292 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60235573 | TCATTTGGCAATGAG[A/T]GTATATATCAGTTGG | 84669 |
rs774925599 | in-del | -/TAA | | | intron-variant | USP32 | GRCh38.p7 | 17:60279855 | AATAATAATAATTAA[-/TAA]TAATAATAATAATAA | 84669 |
rs774942365 | snp | A/G | 1.64849e-05 | 0.00287092 | synonymous-codon, intron-variant | USP32 | GRCh38.p7 | 17:60288572 | AGGAGTATCACTATC[A/G]TCAGTGAGGGTAACA | 84669 |
rs774950912 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60318739 | ATTTTACTGAATTAA[A/T]GATATCCTACATCAT | 84669 |
rs774954961 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60404864 | ACCAAGGAGTAATCA[C/T]TACTAAATGTCCCAT | 84669 |
rs774964837 | snp | A/C | 1.67211e-05 | 0.00289142 | intron-variant | USP32 | GRCh38.p7 | 17:60214580 | AAAATTAAACAAATA[A/C]CAACAATCAGACTCT | 84669 |
rs775017109 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393071 | CGTCCCATTTCCCAC[C/T]GTTTTTCATCTTGCA | 84669 |
rs775018808 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60373125 | TTGAGCCCAGGAGCT[C/T]GAGGCTACAGTAAGC | 84669 |
rs775020407 | snp | C/G | 1.8789e-05 | 0.00306499 | intron-variant | USP32 | GRCh38.p7 | 17:60269419 | CTCTCTACATAGTTT[C/G]CAATTTTTTGACAAT | 84669 |
rs775027939 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60193957 | AGAAAGCTGTGCAGC[-/A]CTTCCCTTCTGAAAA | 84669 |
rs775047853 | in-del | -/CA | | | intron-variant | USP32 | GRCh38.p7 | 17:60250033 | ATTTTAAAAAAAACC[-/CA]CAGATGAAATGAACC | 84669 |
rs775048340 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60303737 | AGTCACAGAAAGAAG[A/G]AAAAACCCAATATAT | 84669 |
rs775067751 | in-del | -/AAGAG | 1.67186e-05 | 0.0028912 | intron-variant | USP32 | GRCh38.p7 | 17:60209554 | GTCCACTATAAATAT[-/AAGAG]AAGTCACAGTCATTA | 84669 |
rs775106277 | snp | A/G | 1.67203e-05 | 0.00289134 | intron-variant | USP32 | GRCh38.p7 | 17:60211365 | GAGGCCAGTGACTCC[A/G]GAAAGATTACCTGTT | 84669 |
rs775108236 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60188794 | AATCCCAATTTAAAC[C/T]ACGGTATCTCTTTTG | 84669 |
rs775116049 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60322517 | AAAATAGATTGTAAT[-/A]AATAGATGTAATTTC | 84669 |
rs775130823 | snp | A/C | | | intron-variant | USP32 | GRCh38.p7 | 17:60351392 | AATTTGTACCTTTAG[A/C]TGATTTTTTTCAACA | 84669 |
rs775134244 | snp | C/G | 1.73231e-05 | 0.002943 | intron-variant | USP32 | GRCh38.p7 | 17:60269568 | CAAACCTGTAAAATA[C/G]GAAGAGATGCCATAA | 84669 |
rs775148437 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60387405 | CTCAATTATTGAGCA[G/T]ATACTATAAAATGAG | 84669 |
rs775158799 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60344632 | TTTTTTTGGTTGCTG[-/T]TTTTAAGTAGAGATG | 84669 |
rs775186604 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60359335 | ACAAAGAAACTGCCT[G/T]ATTTATATGTATCCC | 84669 |
rs775209208 | snp | C/G | 1.80036e-05 | 0.00300024 | intron-variant, downstream-variant-500B | USP32, SCARNA20 | GRCh38.p7 | 17:60231509 | CTTTTATTTCCCACT[C/G]AACTACACATGTCTG | 84669 |
rs775211896 | snp | C/G/T | 3.5389e-05 | 0.00420636 | missense | USP32 | GRCh38.p7 | 17:60208759 | TCTTGCATTTTACTT[C/G/T]AGATCTTAGCTGCCC | 84669 |
rs775224154 | snp | A/G | 0.000670354 | 0.0182956 | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60392577 | GGACCTAACATGGAA[A/G]ACCGCAGAATCTTAG | 84669 |
rs775234292 | snp | A/G | 8.23676e-05 | 0.00641693 | missense | USP32 | GRCh38.p7 | 17:60345522 | CCCCAAGCACTTCCC[A/G]GATGAAGCAGTGCTG | 84669 |
rs775236302 | snp | C/T | 8.09504e-05 | 0.0063615 | intron-variant | USP32 | GRCh38.p7 | 17:60255290 | CATGTTAGGAACATC[C/T]TTTTTTTCTTTTTTT | 84669 |
rs775261728 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60183694 | ACAGCCACGTGACTG[C/T]GCAGTGGGTACTGCC | 84669 |
rs775306312 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60388529 | TACACAAGCCACAAA[C/G]TTAGATGCAACAAGG | 84669 |
rs775306775 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60245114 | ACAACATGGTTTTAT[-/A]ATTATTGTCATGTAA | 84669 |
rs775312380 | snp | C/T | 1.66726e-05 | 0.00288722 | intron-variant | USP32 | GRCh38.p7 | 17:60205398 | AAAATGACTATTTCA[C/T]AAATGACACTAGCAA | 84669 |
rs775319663 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60289924 | GTAGCATCCCATTAA[G/T]TGAGGCGATACTTTT | 84669 |
rs775328825 | snp | A/G | 3.3083e-05 | 0.00406699 | synonymous-codon | USP32 | GRCh38.p7 | 17:60301684 | CCCTTTGGATGTTCC[A/G]CCAAAAGAACAGTAA | 84669 |
rs775345410 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60370889 | TCTCTTGAGGCCAGG[A/G]GTTTGGGACCAGCCT | 84669 |
rs775361444 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60298870 | GCTCATGTTTGTAAT[C/T]CTAGCACTTTGGAAG | 84669 |
rs775375215 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60225018 | TTGGCCTGAAATATA[C/T]ATAGAATCTGATGTG | 84669 |
rs775382927 | in-del | -/CAAA | 0.000115482 | 0.00759787 | intron-variant | USP32 | GRCh38.p7 | 17:60236269 | AGAAATTAAATACAT[-/CAAA]CAAAGTGTGAAATAG | 84669 |
rs775390696 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60199034 | GGTGGGAGGATTGCC[C/T]GAGTCTGGCAAGTTG | 84669 |
rs775396092 | in-del | -/ATTA | | | intron-variant | USP32 | GRCh38.p7 | 17:60360763 | GGTTGTTGTGCTGGG[-/ATTA]ATTTTTTAAATTAGT | 84669 |
rs775400187 | snp | C/T | 1.65861e-05 | 0.00287972 | missense | USP32 | GRCh38.p7 | 17:60205491 | CTGTAAAGGGGCTGT[C/T]AGGAAGAGATGGCAT | 84669 |
rs775405099 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60321035 | AAGTATATGGCACAG[C/T]AGTATAACTAAAAAC | 84669 |
rs775417405 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60365418 | CACAGAAGGTGAAGG[G/T]TGCAGTGAGCCAAGA | 84669 |
rs775422451 | in-del | -/A | | | intron-variant | USP32 | GRCh38.p7 | 17:60398815 | AGACCCTGTCTCTAC[-/A]AAAAAAAAAAATTTA | 84669 |
rs775426346 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60276406 | ATTCCTAAATAAGAT[A/G]TCTGTCTATTCCATT | 84669 |
rs775465924 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60244911 | AGCTGGGATTACAGG[C/T]GTGAGCCATGGCACC | 84669 |
rs775472283 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60396377 | CCACCACGCCTGTCC[C/T]GAAGCTATTTTTGTA | 84669 |
rs775474541 | snp | A/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60384335 | CTGGGGCAACCAAGC[A/T]TCTTTACAGAAATGA | 84669 |
rs775488235 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60188296 | TTCTGATTACTAGGT[A/G]TAATATTCATGTTGG | 84669 |
rs775512185 | snp | C/T | 6.68606e-05 | 0.00578151 | intron-variant, synonymous-codon | USP32 | GRCh38.p7 | 17:60219632 | TCTTAAGTTACCTCT[C/T]GGTAAATGCTGAGGA | 84669 |
rs775544743 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60412293 | GAAGATTGCTTGAGC[C/T]CAGGAGTTTGAGACC | 84669 |
rs775546262 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60240648 | GAAGCTCAGCCAGAG[A/G]TGAAAGTTTACGGGT | 84669 |
rs775549745 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60353234 | AGAGGAAAGAGCATG[C/T]ATGGATGCAACGAGC | 84669 |
rs775592622 | snp | A/G | 3.14441e-05 | 0.00396498 | intron-variant | USP32 | GRCh38.p7 | 17:60207168 | TGAGAAGGGGGAGAT[A/G]TTTCAGATAAAATGG | 84669 |
rs775603775 | snp | A/T | 1.65181e-05 | 0.00287381 | intron-variant | USP32 | GRCh38.p7 | 17:60214814 | GAAAAAAGGCAGATG[A/T]GAAAAAGAAGCACCC | 84669 |
rs775614460 | snp | A/G | | | upstream-variant-2KB, intron-variant, missense | USP32 | GRCh38.p7 | 17:60392347 | AGCTAACCGCGCGCA[A/G]GAGCGCCGGGGAGGG | 84669 |
rs775629937 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60255511 | CACTATGTTGGCCAG[A/G]CTGGTCTTGAACTCC | 84669 |
rs775633057 | snp | A/G | 4.96405e-05 | 0.00498175 | intron-variant | USP32 | GRCh38.p7 | 17:60214606 | ACTCTCTATGACTCT[A/G]AGATGCCTCTTACCT | 84669 |
rs775637148 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60328727 | TCTTTGGGGCCCTGC[A/G]GTTCCTGATGTCTCC | 84669 |
rs775639153 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60348426 | AAGTAGAAGAGTATG[C/T]TCTCCAAAGGCCAGG | 84669 |
rs775658698 | in-del | -/C | 7.10581e-05 | 0.0059602 | intron-variant, nc-transcript-variant | USP32, SCARNA20 | GRCh38.p7 | 17:60231620 | TAAGGAGAACAGGGA[-/C]CCCCCAAAGCCCATG | 84669 |
rs775676791 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60212759 | AGAGTAATTTATTCC[-/T]TTTTTTTTTTTTTGA | 84669 |
rs775678943 | snp | A/C | 1.68185e-05 | 0.00289982 | utr-variant-5-prime, intron-variant | USP32 | GRCh38.p7 | 17:60391951 | CCATGCTCCCCTCAT[A/C]CCCTCGGCGGGGGGT | 84669 |
rs775680792 | snp | C/T | 1.65356e-05 | 0.00287533 | missense | USP32 | GRCh38.p7 | 17:60185626 | GCTCGCCGACTCTGC[C/T]CCACACTCTCATGCT | 84669 |
rs775681620 | snp | C/T | 1.65723e-05 | 0.00287852 | intron-variant | USP32 | GRCh38.p7 | 17:60294678 | ATGTAAATCTTTAAC[C/T]ATACCTCTGAGAAAC | 84669 |
rs775685619 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60307518 | GAGAATCCTAAAACA[C/T]ACATGGAACCTCAAA | 84669 |
rs775692594 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60345950 | CCATGCCGCCGCACT[C/T]CAGCATGGACAACAG | 84669 |
rs775700692 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60184040 | GCCTATAAACCCCGC[A/G]CTTTGGGAGGCCAAG | 84669 |
rs775707507 | snp | C/T | 0.000132229 | 0.00813001 | synonymous-codon | USP32 | GRCh38.p7 | 17:60223414 | AAAATTACTTACCTT[C/T]ACTGGTTCTTGAGTT | 84669 |
rs775723014 | snp | C/G | 1.64735e-05 | 0.00286993 | synonymous-codon | USP32 | GRCh38.p7 | 17:60226142 | TCCAATTCTATCTTC[C/G]ACCTGCTCCATAGGA | 84669 |
rs775748034 | snp | G/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60256801 | GTGAAGAGAGGGTTT[G/T]AATTCATACTTATAG | 84669 |
rs775749225 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, downstream-variant-500B | USP32, CA4 | GRCh38.p7 | 17:60179418 | GTGTCAATTTCATCC[A/G]GGTGAAGTTCCTGAA | 84669 |
rs775752851 | snp | A/C/G/T | 0.000105296 | 0.00725527 | missense | USP32 | GRCh38.p7 | 17:60181718 | CTGGAGGGACAGCTG[A/C/G/T]TTCCACTTTTTCTTG | 84669 |
rs775786927 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60366365 | GGTTTCACTATGTTG[A/G]CCAGGCTGGTCTTGA | 84669 |
rs775809734 | in-del | -/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60180029 | ATTAACTAACTCCTG[-/T]TTTTTTTTTTTCTTG | 84669 |
rs775810462 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60293609 | TGCTAGGCTCAAAAG[C/T]AAGAAAGAGATATCA | 84669 |
rs775824262 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60302416 | CCTCCCAAAGTGCCG[C/G]CATTATAGGCATGAG | 84669 |
rs775830160 | snp | C/T | | | intron-variant | USP32, LOC105371850 | GRCh38.p7 | 17:60416491 | GTATATGGCACATAT[C/T]TGGATTAAAAAAAAT | 84669 |
rs775836734 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | USP32 | GRCh38.p7 | 17:60265439 | ATGTGCATTCAGTAT[A/G]CCTTCTACAATATCA | 84669 |
rs775845161 | snp | A/C/G | 4.94273e-05 | 0.00497108 | synonymous-codon | USP32 | GRCh38.p7 | 17:60180611 | ATAAGTGACGTAATG[A/C/G]CCCCCACCCAGAATT | 84669 |
rs775845682 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60397124 | GAATAAGTACACCAG[C/T]TGAATTCTAATCAGC | 84669 |
rs775858497 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60212799 | GCTTTGTCCCCCCAG[A/G]TTGGAGTGCAGTGAT | 84669 |
rs775865187 | snp | A/G | 3.76145e-05 | 0.00433657 | intron-variant | USP32 | GRCh38.p7 | 17:60207014 | AGGAGTTCTAGTTCT[A/G]TCTTACCTGTCTGTG | 84669 |
rs775868804 | snp | C/G | 1.66291e-05 | 0.00288345 | synonymous-codon | USP32 | GRCh38.p7 | 17:60181612 | CTCTTTACTACTTGA[C/G]AGTTTATTTTTGCTG | 84669 |
rs775870343 | in-del | -/ACATTCATTTACTCTTAACAAATCC | | | intron-variant | USP32 | GRCh38.p7 | 17:60399139 | TAAATAAGAAAGCAG[-/ACATTCATTTACTCTTAACAAATCC]ACTGTGCCTACTCTG | 84669 |
rs775895687 | in-del | -/T | | | upstream-variant-2KB, intron-variant | USP32 | GRCh38.p7 | 17:60393086 | GTTTTTCATCTTGCA[-/T]AAAGGGAAACTCTGT | 84669 |
rs775905166 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60315990 | TGTGACACTGAACCT[C/T]ATCACAAGTCCACTG | 84669 |
rs775924508 | snp | C/T | | | intron-variant | USP32 | GRCh38.p7 | 17:60282351 | TTCCCCCTAAAAACA[C/T]AGTATACTCTTTTTT | 84669 |
rs775943362 | snp | C/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60374228 | ACACCTTAGCCTAGG[C/G]CTACACAGCATCAAG | 84669 |
rs775946313 | in-del | -/TC | 2.4821e-05 | 0.00352276 | frameshift-variant | USP32 | GRCh38.p7 | 17:60211039 | ATGGGGCAACATTCT[-/TC]TGAGTTCCACTCCAA | 84669 |
rs776048327 | snp | A/G | | | intron-variant | USP32 | GRCh38.p7 | 17:60238566 | CCAGCACTTTGGGAG[A/G]CCGAGGCAGGCAGAT | 84669 |