SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs747423 | snp | C/T | 0.310386 | 0.242597 | intron-variant | USP36 | GRCh38.p7 | 17:78788699 | AGATGTGGAGGGACT[C/T]GGGTCCATGGGGTAG | 57602 |
rs867596 | snp | C/T | 0.481242 | 0.0950111 | intron-variant | USP36 | GRCh38.p7 | 17:78795135 | GTCTGAAGGCATTTG[C/T]GTTGTAGCCTGGGCA | 57602 |
rs900348 | snp | G/T | 0.322721 | 0.23919 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837347 | CCCACTCTCCTGCTT[G/T]GCTTTTCTTCTTCTC | 57602 |
rs900349 | snp | A/G | 0.492435 | 0.0610346 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836051 | TGACGAAGTGGATGG[A/G]CTTAAATATTGACTA | 57602 |
rs931226 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | USP36 | GRCh38.p7 | 17:78824498 | agagtgcagtggtgc[A/G]atctccgctcacggc | 57602 |
rs1044486 | snp | C/T | 0.442113 | 0.159977 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796097 | ACATACATTCGTTAA[C/T]TCTTGGGCAGTGGTG | 57602 |
rs1057040 | snp | C/T | 0.499029 | 0.0220079 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803713 | CTGGGCTCAGAGACG[C/T]GCCTCCCACAGCACA | 57602 |
rs1108430 | snp | A/G | 0.128632 | 0.218563 | intron-variant | USP36 | GRCh38.p7 | 17:78792617 | caactggtgttttaa[A/G]gagcccctggcaatt | 57602 |
rs1110274 | snp | G/T | 0.493703 | 0.0557558 | intron-variant | USP36 | GRCh38.p7 | 17:78814202 | TTCTCAGACTTGCAG[G/T]GAGACACGGAAGAGG | 57602 |
rs1317718 | snp | A/G | 0.361684 | 0.223667 | intron-variant | USP36 | GRCh38.p7 | 17:78789158 | CCAGGCTGGGGTGCA[A/G]TGGCGCAATCTCGAC | 57602 |
rs1531797 | snp | A/G | 0.439085 | 0.163545 | intron-variant | USP36 | GRCh38.p7 | 17:78826086 | CCAGGTCTGCCCTTC[A/G]GTGAACTGGGTAATT | 57602 |
rs1531798 | snp | C/T | 0.49614 | 0.0437598 | intron-variant | USP36 | GRCh38.p7 | 17:78826049 | CTGTTCCCTGTGTGC[C/T]GGGCCCCATAGCTAG | 57602 |
rs2054623 | snp | A/G | 0.00872282 | 0.0654624 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807148 | GAGATGGGCCGCTCC[A/G]CTCCTGGGGGTCTGG | 57602 |
rs2054624 | snp | C/T | 0.237593 | 0.249692 | intron-variant | USP36 | GRCh38.p7 | 17:78806016 | GATCTTGGTCAGTGA[C/T]GCCCCCCTGTACCTC | 57602 |
rs2277701 | snp | G/T | 0.0539704 | 0.155153 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78840779 | CGGGCCGAAGGAGTC[G/T]CCAGGGCTGCGTAGG | 57602 |
rs2277702 | snp | C/T | 0.117537 | 0.212022 | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840488 | GCCGGGCTGTCCTCG[C/T]CGGTCTCCGCCGTCC | 57602 |
rs2277703 | snp | C/G | 0.183886 | 0.241099 | intron-variant | USP36 | GRCh38.p7 | 17:78838839 | TCGTGGTAGAGGGTT[C/G]CCGGTGCGCGCCGCA | 57602 |
rs2277704 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838678 | TACATTCAGGAGCTC[C/T]GCGTAGCACCTGCCC | 57602 |
rs2279308 | snp | C/T | 0.496681 | 0.0405994 | intron-variant | USP36 | GRCh38.p7 | 17:78798899 | AGGGAAGGTATGATG[C/T]GTGATGCTGACCACA | 57602 |
rs2279309 | snp | A/G | 0.167158 | 0.235875 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796751 | TAAGTCCAACACCAC[A/G]TTGTCCATCTCCACC | 57602 |
rs2279310 | snp | C/T | 0.182933 | 0.240836 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796788 | GACTCCGGGAGGAAA[C/T]GACGGGGACAGACCC | 57602 |
rs2306525 | snp | A/G | 0.0153263 | 0.0861874 | intron-variant | USP36 | GRCh38.p7 | 17:78802289 | GTGGGAACCGCATGG[A/G]TGTGCACCGGGCGAG | 57602 |
rs2306526 | snp | A/G | 0.496235 | 0.0432229 | intron-variant | USP36 | GRCh38.p7 | 17:78802280 | GCATGGGTGTGCACC[A/G]GGCGAGGGGTTGGGG | 57602 |
rs2306527 | snp | A/G | 0.476833 | 0.105105 | intron-variant | USP36 | GRCh38.p7 | 17:78802073 | GCGTGGGTGTGCACC[A/G]GGTGAGGGGGTATTG | 57602 |
rs2376827 | snp | C/T | 0.181659 | 0.240478 | intron-variant | USP36 | GRCh38.p7 | 17:78788217 | GTCGCCAGGCTGGAG[C/T]GCAGTGGTGCAATCT | 57602 |
rs2376828 | snp | C/T | 0.453331 | 0.145452 | intron-variant | USP36 | GRCh38.p7 | 17:78816758 | ctgacattagagttg[C/T]gagccattgtgccca | 57602 |
rs2376829 | snp | C/T | 0.448452 | 0.152042 | intron-variant | USP36 | GRCh38.p7 | 17:78817043 | ccacatatacaacag[C/T]gatcccataagatta | 57602 |
rs2889479 | snp | C/T | 0.496416 | 0.0421803 | intron-variant | USP36 | GRCh38.p7 | 17:78788116 | caggaagcgagtaca[C/T]GAAGCTCTGCAAGTT | 57602 |
rs3068285 | in-del | -/G | 0.496314 | 0.0427728 | intron-variant | USP36 | GRCh38.p7 | 17:78813270 | CACCAGAAAGCAAGA[-/G]ACCTCAAACACCTCA | 57602 |
rs3068286 | in-del | -/CC | | | intron-variant | USP36 | GRCh38.p7 | 17:78813273 | CAGAAAGCAAGAACC[-/CC]TCAAACACCTCAGCC | 57602 |
rs3088040 | snp | A/G | 0.495057 | 0.0500417 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803778 | CCAGTGAGCCCCCCC[A/G]GAGCCCCTCTGAGAA | 57602 |
rs3744791 | snp | G/T | 0.0433397 | 0.140682 | intron-variant | USP36 | GRCh38.p7 | 17:78827178 | GGTGGCAGCAGAACA[G/T]TCCTATGGCAACAGC | 57602 |
rs3744792 | snp | A/C | 0.0179029 | 0.0929027 | intron-variant | USP36 | GRCh38.p7 | 17:78827145 | GCCCGGCACCTTTCT[A/C]CCCAGGCTGCCCTTG | 57602 |
rs3744793 | snp | A/G | 0.489343 | 0.0722135 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821008 | GACCCCTACTTGGAC[A/G]TCGCGCTGGAGATCC | 57602 |
rs3744794 | snp | A/G | 0.000197772 | 0.00994217 | intron-variant | USP36 | GRCh38.p7 | 17:78818656 | CCAAGGTGAGCGCTC[A/G]TGACACCATCCCAGG | 57602 |
rs3744795 | snp | A/G | 0.0758518 | 0.179367 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807577 | GATTGGTGTGCCCAT[A/G]TCCAGGAATGGCTCC | 57602 |
rs3744796 | snp | A/G | 0.0119854 | 0.0764792 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807115 | CGATTCTCAGGAAAC[A/G]AACTGTTCCACCGCT | 57602 |
rs3744797 | snp | G/T | 0.0221062 | 0.102783 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803753 | TGAGAAGAGGAAAAA[G/T]ACCTTTGTGGGAGAG | 57602 |
rs3744799 | snp | A/G | 0.495818 | 0.0455352 | intron-variant | USP36 | GRCh38.p7 | 17:78798692 | TGCAGGTCGCCGTGC[A/G]CAGGGGTCATTGTGA | 57602 |
rs3744800 | snp | C/T | 0.497473 | 0.0354532 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797743 | ACAGACCGCCCAACA[C/T]AGAGGCTTTGAGGCT | 57602 |
rs3744801 | snp | C/T | 0.499995 | 0.00159744 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797646 | GTGAGCAGAGGTGGC[C/T]GCACACCTGCTGGAC | 57602 |
rs3744802 | snp | C/T | 0.446641 | 0.154377 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797518 | GGTGGCCACATGTCC[C/T]CCAGGTGGTCTCCCG | 57602 |
rs3744803 | snp | A/G/T | 0.0490535 | 0.14873 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797451 | CTTCTCGGGGCTGAC[A/G/T]CCACCGTTGTGTCCG | 57602 |
rs3809895 | snp | A/G | 0.0437281 | 0.141251 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842763 | TGCATTAACAGAATA[A/G]TTGTATTGTCACCCA | 57602 |
rs3826552 | snp | C/T | 0.446641 | 0.154377 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797803 | GTGTGGGCTCTGCTG[C/T]GCTGGGAGCCTGTCA | 57602 |
rs4352096 | snp | C/T | 0.496314 | 0.0427728 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837834 | AGTGAAAGTAAGGAC[C/T]TCCTCCAGCACCTCA | 57602 |
rs4602087 | snp | A/G | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78816870 | aagtatatacTGATG[A/G]ACATGCAGAAcatca | 57602 |
rs4796800 | snp | A/G | 0.248188 | 0.249993 | intron-variant | USP36 | GRCh38.p7 | 17:78808465 | TATGTTGCCCCGGCT[A/G]GCCTTGAATTCCTGA | 57602 |
rs4796817 | snp | C/T | 0.463559 | 0.129972 | intron-variant | USP36 | GRCh38.p7 | 17:78806566 | GCTGCCCAAGCTTCC[C/T]GCTGCAGAGGTGCCG | 57602 |
rs4796819 | snp | A/G | 0.230603 | 0.249246 | intron-variant | USP36 | GRCh38.p7 | 17:78840332 | GAAGGTGCCCGCCCC[A/G]GGGCCGCACCCGCCC | 57602 |
rs4796820 | snp | A/G | 0.214239 | 0.247429 | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840446 | CAGCGGGCCCCGGCG[A/G]CCCCCATCACCGGCC | 57602 |
rs6501249 | snp | A/G | 0.496348 | 0.0425753 | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787560 | ATCTCCGTTAGGGGC[A/G]CTGTTCGTGTGCTGG | 57602 |
rs6501250 | snp | C/T | 0.497271 | 0.0368399 | intron-variant | USP36 | GRCh38.p7 | 17:78812644 | GCAGTGAGCCGAGAT[C/T]GGAGATCGCACCACT | 57602 |
rs6501252 | snp | C/T | 0.130694 | 0.219696 | intron-variant | USP36 | GRCh38.p7 | 17:78817300 | gcccttgtggttaca[C/T]gacacctgaGTCTAC | 57602 |
rs6501253 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78825617 | ATTCCTCCCATCTCA[C/T]AGCCCCAAATCCAAA | 57602 |
rs7206939 | snp | A/G | 0.134802 | 0.221877 | intron-variant | USP36 | GRCh38.p7 | 17:78820420 | gtgagctatgattgc[A/G]ccactgcactcctgc | 57602 |
rs7207007 | snp | A/C | 0.135143 | 0.222054 | intron-variant | USP36 | GRCh38.p7 | 17:78820601 | AAGGCAGACCACCCT[A/C]CCGCACCCTGTAGCT | 57602 |
rs7207012 | snp | C/G | 0.148326 | 0.228391 | intron-variant | USP36 | GRCh38.p7 | 17:78820607 | GACCACCCTCCCGCA[C/G]CCTGTAGCTGCAGCA | 57602 |
rs7207246 | snp | A/G | 0.134802 | 0.221877 | intron-variant | USP36 | GRCh38.p7 | 17:78820830 | GAAAAACTCTAGAAA[A/G]AAACAGGTAAAGACA | 57602 |
rs7208551 | snp | G/T | 0.134802 | 0.221877 | intron-variant | USP36 | GRCh38.p7 | 17:78820811 | AATAAAAGGATACGC[G/T]TAGGAAAAACTCTAG | 57602 |
rs7208858 | snp | C/T | 0.139564 | 0.224285 | intron-variant | USP36 | GRCh38.p7 | 17:78810247 | cccccaacagcttac[C/T]gaataTTCTCTGTGC | 57602 |
rs7209141 | snp | A/G | 0.139225 | 0.224118 | intron-variant | USP36 | GRCh38.p7 | 17:78810973 | acaaaaattagccgg[A/G]agtgctggcgggcac | 57602 |
rs7210763 | snp | C/T | 0.0157215 | 0.0872558 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814538 | TATGTTGAGGAATTC[C/T]GGATAGCCTACATCC | 57602 |
rs7210788 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | USP36 | GRCh38.p7 | 17:78825194 | GTCTCAGCAGCCACC[A/G]CCAAGCATGCAGGAA | 57602 |
rs7211645 | snp | C/T | 0.34303 | 0.232046 | intron-variant | USP36 | GRCh38.p7 | 17:78807874 | ACACCTGGCTAATTT[C/T]TGTATTTTTGACAGA | 57602 |
rs7211960 | snp | C/T | 0.386694 | 0.20932 | intron-variant | USP36 | GRCh38.p7 | 17:78808026 | ATATCTTTATGGCCA[C/T]CTTTACTATAAAACC | 57602 |
rs7212126 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | USP36 | GRCh38.p7 | 17:78808132 | ATAACCATGCATTAA[C/T]ATTCTAGTGCTTTCT | 57602 |
rs7212290 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | USP36 | GRCh38.p7 | 17:78826716 | GGCAACCATCACATA[C/T]AAGGGCTTACGTGGC | 57602 |
rs7213204 | snp | C/T | 0.496649 | 0.0407971 | intron-variant | USP36 | GRCh38.p7 | 17:78835718 | GCTTGGCTAAAGAAT[C/T]CAAGGGCCCCTCTAT | 57602 |
rs7215525 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | USP36 | GRCh38.p7 | 17:78840116 | GGCCGCGGACACAGC[A/G]ACCCGAGCACCTCTC | 57602 |
rs7216266 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78827571 | AGGCTTGAGCATTCA[C/T]TACTGCACAGACAAG | 57602 |
rs7216559 | snp | G/T | 0.189576 | 0.242588 | intron-variant | USP36 | GRCh38.p7 | 17:78827576 | TGAGCATTCACTACT[G/T]CACAGACAAGGAAGA | 57602 |
rs7216626 | snp | A/G | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78827802 | tagtcccagctactt[A/G]ggtggctgaggcagg | 57602 |
rs7217047 | snp | A/G | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78827844 | agcctaggaggttga[A/G]gctgcagtgagctat | 57602 |
rs7217654 | snp | A/G | 0.304188 | 0.244057 | intron-variant | USP36 | GRCh38.p7 | 17:78815225 | TAGTTCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 57602 |
rs7217867 | snp | C/T | 0.141258 | 0.225111 | intron-variant | USP36 | GRCh38.p7 | 17:78822527 | CGGCTCTGCACCCGT[C/T]TCAGAGAGGACAGCG | 57602 |
rs7218057 | snp | C/T | 0.169435 | 0.236663 | intron-variant | USP36 | GRCh38.p7 | 17:78822670 | CCCGGGGCTGCCTGG[C/T]GCCTCCCACGCCTAC | 57602 |
rs7218605 | snp | C/T | 0.494774 | 0.0508504 | intron-variant | USP36 | GRCh38.p7 | 17:78815721 | ATAGAAAAAAataca[C/T]gcacacatatacata | 57602 |
rs7219360 | snp | C/T | 0.134119 | 0.221521 | intron-variant | USP36 | GRCh38.p7 | 17:78822702 | TATCCATATGGTAGC[C/T]ACTCACGCTGGAAGG | 57602 |
rs7220532 | snp | C/T | 0.497211 | 0.037236 | intron-variant | USP36 | GRCh38.p7 | 17:78812691 | GACAGAGCGAGACTC[C/T]GTCTCGAAAAAAAAA | 57602 |
rs7222131 | snp | A/G | 0.337841 | 0.23406 | intron-variant | USP36 | GRCh38.p7 | 17:78820117 | AGGCAGCAAATCACA[A/G]AACTTAGACTCGCAT | 57602 |
rs7223832 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78804664 | AAAAAGCAAGCCAAC[A/C]CGTGATTTTAAAAGT | 57602 |
rs7224190 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78832438 | CAAGATAGTAAGATG[C/T]ACTAATATTTCACAG | 57602 |
rs7224341 | snp | A/G | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78832601 | cggggatttacagat[A/G]ttatctagttttaac | 57602 |
rs7224531 | snp | A/G | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78832760 | TGAGACGAAAACAAC[A/G]GCCATCTAGTCAAAT | 57602 |
rs7224590 | snp | A/G | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78832540 | cttactcacacgctt[A/G]ctgctgacatgctgc | 57602 |
rs7225821 | snp | A/G | 0.213937 | 0.247385 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841775 | TGTGTCTTTTTTGAT[A/G]TAAGTAGGAATGATG | 57602 |
rs7226033 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | USP36 | GRCh38.p7 | 17:78792706 | TCACTATGATCCCCC[C/T]GGGAAGGtttttttt | 57602 |
rs7226043 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78825683 | GAATTTCTTCCACCG[C/T]AGACTCTGGTTAATT | 57602 |
rs7226193 | snp | A/G | 0.335788 | 0.23482 | intron-variant | USP36 | GRCh38.p7 | 17:78820596 | CAGCAAAGGCAGACC[A/G]CCCTCCCGCACCCTG | 57602 |
rs7226316 | snp | A/G | 0.169435 | 0.236663 | intron-variant | USP36 | GRCh38.p7 | 17:78792758 | gagtctcactctgtc[A/G]cccaggctggagtgc | 57602 |
rs8064351 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78825941 | ATTGGCCACACCACA[C/T]TGCAAACGCTGCTGG | 57602 |
rs8065170 | snp | A/G | 0.0191375 | 0.0959297 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821009 | GATCTCCAGCGCGAC[A/G]TCCAAGTAGGGGTCG | 57602 |
rs8068534 | snp | A/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78826267 | aggaatggtggctca[A/T]gcctgtaatcccagc | 57602 |
rs8069001 | snp | C/T | 0.134802 | 0.221877 | intron-variant | USP36 | GRCh38.p7 | 17:78821279 | TTGCACTCACAGGGC[C/T]CTCCCTGCCTGGACT | 57602 |
rs8069028 | snp | A/C | 0.135143 | 0.222054 | intron-variant | USP36 | GRCh38.p7 | 17:78821381 | TGCACGGCACTTCCT[A/C]ATGAGAatatatata | 57602 |
rs8069157 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78821420 | tatatatatatatat[A/T]ttttttttttttttt | 57602 |
rs8069830 | snp | C/T | 0.186737 | 0.241863 | intron-variant | USP36 | GRCh38.p7 | 17:78821776 | GCTCCAGTGGCCAGG[C/T]GGGCCAAGAGTCTCA | 57602 |
rs8071100 | snp | G/T | 0.33875 | 0.233717 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78786996 | tttattttttgagac[G/T]gagtctcgctctgtt | 57602 |
rs8072569 | snp | A/G | 0.495445 | 0.0475058 | intron-variant | USP36 | GRCh38.p7 | 17:78790918 | TGGCAGCCATGTCCT[A/G]TTGCTTCCTCTAATC | 57602 |
rs8073626 | snp | C/T | 0.480931 | 0.0957637 | intron-variant | USP36 | GRCh38.p7 | 17:78794197 | TCTCAGCCAACCTGG[C/T]GGCTGGTCATGCTCA | 57602 |
rs8075902 | snp | A/G | 0.040671 | 0.13668 | intron-variant | USP36 | GRCh38.p7 | 17:78816143 | TGTTTAGGAACTCCG[A/G]AAAACATACGCATAA | 57602 |
rs8076017 | snp | A/C | 0.040671 | 0.13668 | intron-variant | USP36 | GRCh38.p7 | 17:78816152 | ACTCCGAAAAACATA[A/C]GCATAAttttttttt | 57602 |
rs8078042 | snp | A/G | 0.030278 | 0.119257 | intron-variant | USP36 | GRCh38.p7 | 17:78819787 | TATTTAGAAGTTTGA[A/G]TTTTTAGGACACACA | 57602 |
rs8079153 | snp | C/T | 0.492237 | 0.0618148 | intron-variant | USP36 | GRCh38.p7 | 17:78800772 | CCTCCTTGCTGAGCA[C/T]GAGCCCTTACTGTGT | 57602 |
rs8079955 | snp | C/G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78804438 | gcactccagcctggg[C/G/T]gacaaagcaagactc | 57602 |
rs8182240 | snp | A/G | 0.000446117 | 0.0149285 | intron-variant | USP36 | GRCh38.p7 | 17:78820977 | CAAAAGTGAAGGGCA[A/G]GACAGATCTGTACCC | 57602 |
rs8182269 | snp | A/T | 0.490563 | 0.0680388 | intron-variant | USP36 | GRCh38.p7 | 17:78793909 | CCCTGGGTTCCCTGT[A/T]CTGGTAAGATGCCAA | 57602 |
rs9302885 | snp | A/G | 0.495416 | 0.0476568 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803816 | CAACTGGTGTGGAAG[A/G]GACACAAGGTCCTCG | 57602 |
rs9675033 | snp | A/G | 0.177503 | 0.239258 | intron-variant | USP36 | GRCh38.p7 | 17:78800768 | AGCGCCTCCTTGCTG[A/G]GCATGAGCCCTTACT | 57602 |
rs9889651 | snp | A/G | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78830318 | GCTTTACAAAAatcc[A/G]tgttgctagacatag | 57602 |
rs9889908 | snp | A/C/T | 0.000956429 | 0.0218477 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803871 | ATGGAGGAGCAGCTC[A/C/T]GTGGTTCTGACGTCC | 57602 |
rs9890452 | snp | A/G | 0.136847 | 0.222927 | intron-variant | USP36 | GRCh38.p7 | 17:78823401 | CGCCCGCAGGGCCAC[A/G]AGGAATCCCCTCTTG | 57602 |
rs9891151 | snp | A/G | 0.135143 | 0.222054 | intron-variant | USP36 | GRCh38.p7 | 17:78823714 | aagaggcaggcaggc[A/G]gccttagaagggcag | 57602 |
rs9891175 | snp | C/G | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78831934 | cgtgacagagtgaga[C/G]cttgtctcaaaaaaa | 57602 |
rs9893633 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818537 | TTCACAATATGTGTA[A/G]AACCTTTAGAACAGG | 57602 |
rs9894078 | snp | A/G | | | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818691 | CTTCCCCCCGCTGAA[A/G]TTGGCAAAGCGCTTG | 57602 |
rs9895281 | snp | G/T | 0.0320281 | 0.122427 | intron-variant | USP36 | GRCh38.p7 | 17:78827094 | TTTGGGCTCCAACAG[G/T]TTGAGTACCCAGAGG | 57602 |
rs9895282 | snp | C/T | 0.0319174 | 0.122229 | intron-variant | USP36 | GRCh38.p7 | 17:78827095 | TTGGGCTCCAACAGT[C/T]TGAGTACCCAGAGGC | 57602 |
rs9895939 | snp | A/G | 0.134802 | 0.221877 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836565 | GACATATTAGTTCAC[A/G]TTTCCCCCACAAAAA | 57602 |
rs9895988 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836608 | CTACAAATAGAGGTG[A/C]GCAGACAACAGTGGC | 57602 |
rs9899256 | snp | A/C | | | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840421 | GAAGTTGACCTGAAT[A/C]CTGCACAGACAGCGG | 57602 |
rs9900386 | snp | A/C | 0.138546 | 0.223781 | intron-variant | USP36 | GRCh38.p7 | 17:78819346 | gggaggcaaggcagg[A/C]agatcacctgagttc | 57602 |
rs9901315 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | USP36 | GRCh38.p7 | 17:78805670 | AAGGGGCTGCATCTC[C/T]GGCAGGTGTCTGCAG | 57602 |
rs9902176 | snp | C/T | 0.137867 | 0.223442 | intron-variant | USP36 | GRCh38.p7 | 17:78819314 | AGCCGGCTGTAGTAG[C/T]gtgatcccagcactt | 57602 |
rs9908106 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820215 | aacagcggctcacgc[C/T]tataatcccagcacc | 57602 |
rs9909968 | snp | A/G | 0.139225 | 0.224118 | intron-variant | USP36 | GRCh38.p7 | 17:78813567 | ACAGCATCAATGTGA[A/G]GGCAGATGGGATCCT | 57602 |
rs9910776 | snp | C/T | 0.123452 | 0.215605 | intron-variant | USP36 | GRCh38.p7 | 17:78838224 | aaaaatacaaaaaaa[C/T]tagccaggcatggtg | 57602 |
rs9910933 | snp | C/G/T | 0.0380199 | 0.132533 | intron-variant | USP36 | GRCh38.p7 | 17:78821896 | CCTGGGTTCATGTTC[C/G/T]AATCCTGGCAAGAAG | 57602 |
rs9910997 | snp | G/T | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78829708 | tctgcccacccctgC[G/T]CTACATAAAACGCCT | 57602 |
rs9911674 | snp | C/T | 0.00274554 | 0.036949 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803726 | GCGCGTCTCTGAGCC[C/T]AGCCTCTGCGGCTCT | 57602 |
rs9913300 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP36 | GRCh38.p7 | 17:78825889 | CACTTCTCCCAGGAA[A/G]CCGCCTCTGGGTGAG | 57602 |
rs9916289 | snp | C/T | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78829812 | gtggcacaatcttgg[C/T]tcactgcaacctccg | 57602 |
rs9916851 | snp | A/T | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78830138 | ccccattttccatgt[A/T]ccttcattcaaagtc | 57602 |
rs10522788 | in-del | -/T | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78791152 | TTTTTTTTTTTTTTT[-/T]AGCTGGAGTTTCGCT | 57602 |
rs10582083 | in-del | -/CA | | | intron-variant | USP36 | GRCh38.p7 | 17:78815848 | ATACATACACACACA[-/CA]TATGCATGCATACAC | 57602 |
rs10590690 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78804508 | AACAAAAAAAAAAAA[-/A]CAAAGTTACCTAGGT | 57602 |
rs10711355 | in-del | -/A | 0.449345 | 0.150869 | intron-variant | USP36 | GRCh38.p7 | 17:78815710 | ACCAATTTTTCATAG[-/A]AAAAAATACACGCAC | 57602 |
rs11077397 | snp | C/T | 0.441705 | 0.160466 | intron-variant | USP36 | GRCh38.p7 | 17:78800381 | CCCCATCAGCAACAC[C/T]GCACAGGTCCACCCA | 57602 |
rs11409517 | in-del | -/G | 0.496616 | 0.0409947 | intron-variant | USP36 | GRCh38.p7 | 17:78789039 | CCGTCTCTATTAAAA[-/G]TATGAAAATTAGCCG | 57602 |
rs11649885 | snp | A/G | 0.442113 | 0.159977 | intron-variant | USP36 | GRCh38.p7 | 17:78831798 | AGAATACAAAAAAAA[A/G]ATTAGCTGGGCATGG | 57602 |
rs11649964 | snp | C/G | 0.446902 | 0.154045 | intron-variant | USP36 | GRCh38.p7 | 17:78804100 | GGCTTTTACCCTGTA[C/G]TTTTCAGATACACAT | 57602 |
rs11650000 | snp | A/G | 0.494651 | 0.0514399 | intron-variant | USP36 | GRCh38.p7 | 17:78832072 | CATGGACAAATATTT[A/G]TTCATGTAATTTAGG | 57602 |
rs11652626 | snp | C/T | 0 | 0 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841051 | CAGGCGCTCCCGCCC[C/T]TGTGCCGCGGCAGGG | 57602 |
rs11653982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78834924 | agttcaagactacaa[C/T]gagttgtgatggagc | 57602 |
rs11655882 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78831089 | caattagccaggcat[C/G]gtggcacgtgcctgt | 57602 |
rs11658295 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78829624 | cagccatagacaata[C/T]atgaacaatggggta | 57602 |
rs11658299 | snp | C/T | 0.473359 | 0.112298 | intron-variant | USP36 | GRCh38.p7 | 17:78829640 | ATGAACAATGGGGTA[C/T]GAACGTGTTCAATAA | 57602 |
rs11867428 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78804722 | aGGCAAAGTTAATAA[A/G]AATTGTTCCATGCCT | 57602 |
rs11869631 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | USP36 | GRCh38.p7 | 17:78795047 | aaaaaCCACAGCCTC[A/G]CCCATGTCGCCACTG | 57602 |
rs11870366 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796451 | CTCCACTCACTGCTG[C/T]TGGGACACAGGTGGC | 57602 |
rs11870759 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | USP36 | GRCh38.p7 | 17:78809205 | AGTAAATTATGTACA[A/G]AAATGTAAATCTTAG | 57602 |
rs12103553 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP36 | GRCh38.p7 | 17:78833719 | ACATCCTGCATTCCT[A/G]GGATAAACATAAGTT | 57602 |
rs12103607 | snp | A/G/T | 0.143907 | 0.229287 | intron-variant | USP36 | GRCh38.p7 | 17:78833890 | agaatgagctgggaa[A/G/T]gattctctcctcctc | 57602 |
rs12103727 | snp | C/G | 0.296364 | 0.245663 | intron-variant | USP36 | GRCh38.p7 | 17:78818034 | AGACTGTAGTGAGCG[C/G]TGATTATGCCACTGC | 57602 |
rs12103728 | snp | G/T | 0.296364 | 0.245663 | intron-variant | USP36 | GRCh38.p7 | 17:78818033 | AAGACTGTAGTGAGC[G/T]CTGATTATGCCACTG | 57602 |
rs12103730 | snp | A/G | 0.136847 | 0.222927 | intron-variant | USP36 | GRCh38.p7 | 17:78818095 | gtcttaaaacaaaat[A/G]aaaTTTAAACAATAA | 57602 |
rs12452199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78792535 | cagccccggggacta[C/T]tggacatgcacattc | 57602 |
rs12600666 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78792550 | ttggacatgcacatt[A/C]tcaggcctcatccca | 57602 |
rs12936425 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811155 | aaaaaaaaaaaaaaa[A/G]gaaaCAGTCATCAAG | 57602 |
rs12936793 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78801979 | TGAAGGTTGGTAGGG[G/T]CCCAGGGCCCTCCAC | 57602 |
rs12936955 | snp | C/T | 0.177824 | 0.239355 | intron-variant | USP36 | GRCh38.p7 | 17:78793634 | ACACACAGTCCTCCT[C/T]TACCACCACGTCCTT | 57602 |
rs12942129 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792591 | atcagaatgcggggg[A/T]aggagcccggcaact | 57602 |
rs12942166 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792630 | aaggagcccctggca[A/T]ttctggtgctcactt | 57602 |
rs12942382 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792633 | gagcccctggcaatt[C/T]tggtgctcacttgag | 57602 |
rs12942641 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792664 | tttgagaCCAGGGAC[C/T]AGGATGGCAACTCTC | 57602 |
rs12942645 | snp | A/G | 0.106987 | 0.205054 | intron-variant | USP36 | GRCh38.p7 | 17:78808234 | CTCAAGCATTTTTAT[A/G]GGCGATAACTCTCAA | 57602 |
rs12942851 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792594 | agaatgcgggggaag[A/G]agcccggcaactggt | 57602 |
rs12948018 | snp | A/G | 0.496681 | 0.0405994 | intron-variant | USP36 | GRCh38.p7 | 17:78833133 | agcctgggcgacaga[A/G]cgagactccatctcc | 57602 |
rs12953123 | snp | A/G | 0.412249 | 0.190198 | intron-variant | USP36 | GRCh38.p7 | 17:78793672 | CCACATCCTCATTGC[A/G]CTGAGGTTGTCCAAG | 57602 |
rs16971728 | snp | A/T | 0.179425 | 0.239831 | intron-variant | USP36 | GRCh38.p7 | 17:78811386 | ATATATGTATGACTA[A/T]GTACGTATGCATATA | 57602 |
rs28409751 | snp | C/T | 0.132066 | 0.220435 | intron-variant | USP36 | GRCh38.p7 | 17:78834897 | GAGATGGGAGGATCA[C/T]GTGAGCCCAGGAGTT | 57602 |
rs28436218 | snp | C/T | 0.132409 | 0.220618 | intron-variant | USP36 | GRCh38.p7 | 17:78826731 | TAAGGGCTTACGTGG[C/T]GTGTGAATAAGAAAC | 57602 |
rs28438597 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP36 | GRCh38.p7 | 17:78800332 | CTGCCATCAGGGGCC[C/T]GACCTCCTAAGCCCT | 57602 |
rs28483679 | snp | G/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78826921 | GTCCATGGTAAGAAC[G/T]GAATGCCCCTAAGAA | 57602 |
rs28489871 | snp | C/G | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78834157 | GAGGCTGAGACAGGA[C/G]AATTGCTTGCACCCA | 57602 |
rs28509325 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841887 | GGGAGAGAGGCTAGA[A/T]GTACTTGGAACAAAA | 57602 |
rs28531934 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790299 | TTCTTTTTCTTTTTC[C/T]TTTTTTTTAAAGACA | 57602 |
rs28557415 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | USP36 | GRCh38.p7 | 17:78834125 | GGTGGCGTGCGTCTA[C/T]AGTCCCAGCTATTTG | 57602 |
rs28559298 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78826783 | CCTAAAGTTATAAAC[C/T]TCCTCATGTTAAAGC | 57602 |
rs28605110 | snp | A/G | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78834533 | CTCACTGCAACCTCC[A/G]CCTTCTGGGTTCAAG | 57602 |
rs28645711 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78834999 | AAAAATAATATTTGT[A/G]TATATATATATATAT | 57602 |
rs28673177 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823547 | GAGAACAGCTGGGCA[A/G]GAATGGAGGAGGGGG | 57602 |
rs33980218 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78831225 | GTGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 57602 |
rs34018899 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78789040 | CGTCTCTATTAAAAT[-/G]ATGAAAATTAGCCGG | 57602 |
rs34056363 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78820386 | GGAGGATCACTTAAG[-/C]CTAGAGGTCAACACT | 57602 |
rs34078860 | snp | A/G | 0.0497574 | 0.149676 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835470 | CGGGGCTGGGACTCC[A/G]TCACCACAGCTCTCA | 57602 |
rs34121152 | snp | C/T | 0.0271774 | 0.11336 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806262 | GACGGAGGTCATTGC[C/T]GGTCGCCCTCCACAG | 57602 |
rs34126628 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78801630 | GGGTGGTGCCCAAGG[-/T]ACAGCCACAGCACAC | 57602 |
rs34184429 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78832061 | TTAAGTGGCACATGG[-/C]ACAAATATTTATTCA | 57602 |
rs34238419 | snp | A/G | 0.122411 | 0.214991 | intron-variant | USP36 | GRCh38.p7 | 17:78794855 | CTACTAAAAATACAA[A/G]AATTAGTCAGGCGTG | 57602 |
rs34274394 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78839263 | ATGGAGAACCGCACA[-/G]GGGAGCACATGAGCC | 57602 |
rs34297492 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78800068 | TGACCTGACACAATA[A/G]AGAAGGCTGTTGTCC | 57602 |
rs34398293 | snp | G/T | 0.022487 | 0.103624 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835437 | AGACAGTCGCTCCGT[G/T]GGGAAAAGCACTTTC | 57602 |
rs34458438 | snp | C/T | 0.00371599 | 0.042944 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798957 | ACCACGGTCTCAGTC[C/T]GGGCCTGTCTGCTGT | 57602 |
rs34503663 | multinucleotide-polymorphism | GC/TG | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78818033 | AAGACTGTAGTGAGC[GC/TG]TGATTATGCCACTGC | 57602 |
rs34518375 | snp | A/G | 0.175254 | 0.238565 | intron-variant | USP36 | GRCh38.p7 | 17:78811088 | GTGAGCTGAGATGGC[A/G]CCACTGCACTCCAGC | 57602 |
rs34531932 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78795085 | GTTGGTGTCAGATCA[-/C]CCACCTCTCCAAGCC | 57602 |
rs34568176 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78812188 | TGAGACCCTGTCTCC[-/A]AAAAAAAAAGTTTGC | 57602 |
rs34645192 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78794962 | CAGTGAGCGGAGAAT[A/C]GTGCCACTGCACTCC | 57602 |
rs34651394 | snp | A/G | 0.00337656 | 0.0409497 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828934 | GACGGGCTTGATGGC[A/G]TTGCCGCTGTTGGCG | 57602 |
rs34691953 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | USP36 | GRCh38.p7 | 17:78840249 | GGACCCCCACGCCAC[C/T]CGCCAGAAGCAGCAG | 57602 |
rs34694901 | snp | C/T | 0.185155 | 0.241444 | intron-variant | USP36 | GRCh38.p7 | 17:78809583 | GCCAATCTCCACCCT[C/T]GGGCATCACTCTGCC | 57602 |
rs34791045 | snp | C/T | 0.188 | 0.24219 | intron-variant | USP36 | GRCh38.p7 | 17:78808957 | AATGAAATTACAGAT[C/T]TCATTTTCATGAAAT | 57602 |
rs34810096 | in-del | -/T | 0.167484 | 0.23599 | intron-variant | USP36 | GRCh38.p7 | 17:78804691 | AAGTCAAAAAAAAAA[-/T]TTTTTTTTTTTTAAA | 57602 |
rs34947941 | in-del | -/GACC | 0.496314 | 0.0427728 | intron-variant | USP36 | GRCh38.p7 | 17:78813271 | ACCAGAAAGCAAGAA[-/GACC]CCTCAAACACCTCAG | 57602 |
rs34984995 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78805624 | AAGAGACGCAGGCAG[-/C]CCCTGCGGACCAGGG | 57602 |
rs34996187 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78799182 | GGAGGACGGCTCGAC[-/A]GCCCATGTGTGGTCG | 57602 |
rs35141467 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78802061 | CTGTGCACTCCCCAA[-/T]ACCCCCTCACCCGGT | 57602 |
rs35161732 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78828624 | TAGCACAGAGGGATT[-/A]CCCAAGACTTCATCC | 57602 |
rs35208777 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809583 | CCAATCTCCACCCTC[-/G]GGGCATCACTCTGCC | 57602 |
rs35262869 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78827156 | GGGTAGAAAGGTGCC[-/G]GGGCTGGCTGTTGCC | 57602 |
rs35273233 | snp | A/G | 0.268819 | 0.249291 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818700 | GCTGAAGTTGGCAAA[A/G]CGCTTGAGGGAAAGG | 57602 |
rs35371422 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78804625 | TGATCCCTGAGATTT[-/A]AAAAAAAAAAAAAAA | 57602 |
rs35635171 | snp | A/T | 0.192715 | 0.243348 | intron-variant | USP36 | GRCh38.p7 | 17:78804703 | AAATTTTTTTTTTTT[A/T]AAAAGGCAAAGTTAA | 57602 |
rs35721231 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813815 | TGGTTCAGAACCACC[-/T]TGACGTTGCTGGAAT | 57602 |
rs35775669 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78840006 | GGTCAACCACGTGCT[-/G]GGGGAGAGGAGCCCA | 57602 |
rs35796533 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78802978 | AGGGTTTAGCTGTCA[-/C]CCCAGGCTGTAGTGC | 57602 |
rs35820493 | snp | A/G | 0.0628225 | 0.165724 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807181 | GGCCTTGGTGGAGTC[A/G]CTGCTGGCCGAGTGC | 57602 |
rs35862601 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795886 | CAACAGACCCAGATC[C/T]TAAGTCAACCAAGTG | 57602 |
rs35863460 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78816071 | GCTGAGTGCACCAGG[-/C]ACAGCACAGAGCCCA | 57602 |
rs35886050 | in-del | -/T | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836164 | GACTAGCTCCCTCTG[-/T]TTTTGGGGTTGAGCA | 57602 |
rs35930734 | in-del | -/A | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842600 | TAAAAAAAAAAAAAA[-/A]GAAAGAAATGCAACG | 57602 |
rs35999286 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78831494 | GCAGTCACCTGTAAT[-/C]CCCAGCTACTTGGGA | 57602 |
rs36097597 | in-del | -/G | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795918 | TGCTATGACAAAGGC[-/G]TTGGGTTATTGACAT | 57602 |
rs55785416 | snp | A/T | 0.138886 | 0.22395 | intron-variant | USP36 | GRCh38.p7 | 17:78816175 | TTTTTTTTTTTTTTT[A/T]AAGAAACACAGTCTC | 57602 |
rs55790511 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78805009 | GGACACAGATGCGTA[A/G]AGCAGAATCATGAGC | 57602 |
rs55890956 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78828097 | GTGTGGTGCGCCTGT[A/G]ATCCCAGCTACTCAG | 57602 |
rs55909837 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78831256 | AAAAAAAAAAAAAGG[-/G]ACAACATAAATATTG | 57602 |
rs55968895 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78805014 | CAGATGCGTAGAGCA[A/G]AATCATGAGCAAGGC | 57602 |
rs56215857 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78804857 | GGTAAGGAAAAAAAA[A/G]ATCCCGTGAGGATTT | 57602 |
rs56262909 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78805594 | ACTCTCAACTTCCTG[C/T]CACTCGAGGCACCTA | 57602 |
rs56301475 | snp | C/T | 0.0155016 | 0.0866632 | intron-variant | USP36 | GRCh38.p7 | 17:78835245 | TCTAATCCAGAGGAC[C/T]CACAGCCACCCCACT | 57602 |
rs56306428 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78804830 | GGAGGAAACCTTCAC[A/G]AAACAATAAATGGTA | 57602 |
rs56404806 | in-del | -/AT/TATT/TT | | | intron-variant | USP36 | GRCh38.p7 | 17:78835017 | ATATATATATATATA[-/AT/TATT/TT]TTTTGGAAGTATCTT | 57602 |
rs56703747 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78821389 | ACTTCCTAATGAGAA[-/T]ATATATATATATATA | 57602 |
rs56743348 | snp | C/T | 0.138546 | 0.223781 | intron-variant | USP36 | GRCh38.p7 | 17:78816279 | ATCCTCCTATCTCTA[C/T]CTCCCAAGTAGCTGG | 57602 |
rs56836334 | in-del | -/GT | | | intron-variant | USP36 | GRCh38.p7 | 17:78788134 | AGCTCTGCAAGTTGT[-/GT]TTAAAATTGCATATG | 57602 |
rs57078433 | snp | C/T | 0.138546 | 0.223781 | intron-variant | USP36 | GRCh38.p7 | 17:78816369 | GATGGCTCACACCTA[C/T]AATCCCAACACTTTG | 57602 |
rs57162507 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | USP36 | GRCh38.p7 | 17:78823374 | TGTCATCCAGAAGCC[C/T]GCAAGCACCAGCGCC | 57602 |
rs57490171 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | USP36 | GRCh38.p7 | 17:78802618 | CCCGCCTGCAACATG[A/G]AGAAGGTGCCACCCC | 57602 |
rs57718722 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78826598 | TTTAAAGTATTTCTA[C/T]GATCCTAAGCTGAGG | 57602 |
rs57732935 | snp | C/T | 0.0201928 | 0.0984309 | intron-variant | USP36 | GRCh38.p7 | 17:78806926 | TTGGAGCTCTCCTGA[C/T]ACACAGCAGCGGCGA | 57602 |
rs57899453 | snp | A/C | 0.339882 | 0.233284 | intron-variant | USP36 | GRCh38.p7 | 17:78829368 | AAAATGAAGCTTAAA[A/C]GATGTATTCTCGAAT | 57602 |
rs58031704 | snp | A/T | 0.084364 | 0.187256 | intron-variant | USP36 | GRCh38.p7 | 17:78788176 | TTTATTTATTTATTT[A/T]TTTTTTTGAGACAGA | 57602 |
rs58053855 | in-del | -/AAG | | | intron-variant | USP36 | GRCh38.p7 | 17:78831252 | AAAAAAAAAAAAAAA[-/AAG]GGACAACATAAATAT | 57602 |
rs58129406 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78812547 | ACAAAAAAAATTAGC[C/T]GGGCGTGGTTCGGGC | 57602 |
rs58132736 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78789316 | GAAAGGTATGATCTA[A/G]AGGTAGCAGCTTTTC | 57602 |
rs58206259 | snp | A/G | 0.0482946 | 0.147699 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796716 | GCCTCTGGCCCAGCA[A/G]AGCCACACTGAAGGA | 57602 |
rs58212356 | snp | C/G | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78829131 | CAAACCAGGCTGTGA[C/G]AGAACGGCTGAGCCA | 57602 |
rs58388020 | snp | C/G | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78829528 | TGAAAATGTTTTCTG[C/G]GAAGATCCAGATAGC | 57602 |
rs58451711 | snp | C/T | 0.139564 | 0.224285 | intron-variant | USP36 | GRCh38.p7 | 17:78809121 | TTCATTTGAATGAGA[C/T]CTTTTGTTTACAAAT | 57602 |
rs58743280 | snp | A/G | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78795010 | GAGACTCTGTTCGGG[A/G]AAAAAAAAAAAAAAA | 57602 |
rs58756152 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78821408 | TATATATATATATAT[-/A]TATATATATATATTT | 57602 |
rs58765502 | snp | A/G | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78829281 | TCACCCCACATTAAT[A/G]CTGACCTGTGCATGA | 57602 |
rs58923077 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78821410 | TATATATATATATAT[-/A]TATATATATATTTTT | 57602 |
rs58951893 | snp | A/G | 0.429688 | 0.173817 | intron-variant | USP36 | GRCh38.p7 | 17:78809317 | CCTCTATTTTCTTCC[A/G]AGTTTTGTTTTGTTC | 57602 |
rs59060228 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | USP36 | GRCh38.p7 | 17:78791198 | GGAATGCAATGGTGC[A/G]ATCTCGGCTCACCGC | 57602 |
rs59230404 | snp | A/G | 0.0417532 | 0.138323 | intron-variant | USP36 | GRCh38.p7 | 17:78828869 | AAATAAATAAATCAC[A/G]AAAATTTTAACATGG | 57602 |
rs59310362 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78821386 | GGCACTTCCTAATGA[-/G]AATATATATATATAT | 57602 |
rs59341814 | snp | G/T | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78829494 | TCTAGTAAACACCTC[G/T]CTAGGATACATCTGG | 57602 |
rs59441706 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78811045 | CTTGAACCCAAGAGG[C/T]GGAGGCTGCATAGTG | 57602 |
rs59562526 | snp | A/G | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78833481 | GCACTCCCTCTTTGC[A/G]GGCTGCTACTCCAGG | 57602 |
rs59755031 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP36 | GRCh38.p7 | 17:78827554 | TTTCTCAATAAGATT[A/G]CAGGCTTGAGCATTC | 57602 |
rs60045444 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | USP36 | GRCh38.p7 | 17:78791360 | TGACCTCAGGTGATC[C/T]GCCCCGCCTAGGCCT | 57602 |
rs60102286 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78821416 | TATATATATATATAT[-/A]TATATTTTTTTTTTT | 57602 |
rs60185023 | snp | C/T | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78830014 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCATCG | 57602 |
rs60315324 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | USP36 | GRCh38.p7 | 17:78834027 | CAAGGCGGTTGGATC[A/T]CCTGAGGTCACGAGT | 57602 |
rs60591019 | snp | A/G | 0.147321 | 0.227941 | intron-variant | USP36 | GRCh38.p7 | 17:78829275 | ACACCATCACCCCAC[A/G]TTAATGCTGACCTGT | 57602 |
rs60805629 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | USP36 | GRCh38.p7 | 17:78830365 | TCTTCCAGCTAGAAT[A/G]TTTCACTGAATGAAG | 57602 |
rs60877034 | snp | A/G | 0.130008 | 0.219321 | intron-variant | USP36 | GRCh38.p7 | 17:78833468 | AGTCACTTCTATAGC[A/G]CTCCCTCTTTGCGGG | 57602 |
rs60943284 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | USP36 | GRCh38.p7 | 17:78825840 | CAACCCTCCTCCTGG[A/G]GACACCTACTTGCCT | 57602 |
rs61035362 | snp | A/G | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78833531 | TTATCGGAGCCTCAC[A/G]CAACTCTGTAAGGAA | 57602 |
rs61159316 | snp | A/C | 0.0482946 | 0.147699 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796528 | AAACAGAAGAAAATC[A/C]AAAAAGAGACACCCA | 57602 |
rs61211697 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | USP36 | GRCh38.p7 | 17:78790554 | CCGTGGCCTCCCAAA[A/G]AGCTGGGACTACAGG | 57602 |
rs61302693 | in-del | -/AG | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78811168 | AAGAAACAGTCATCA[-/AG]AGAGGGTCCACCCCA | 57602 |
rs61553210 | snp | G/T | 0.0441095 | 0.141807 | intron-variant | USP36 | GRCh38.p7 | 17:78825305 | CTGATCATAATGCAA[G/T]TAACATCAAAAGTCA | 57602 |
rs61555105 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | USP36 | GRCh38.p7 | 17:78800228 | AGATCTAAATGGAAT[C/T]CACCTCACCTACGGG | 57602 |
rs61582072 | snp | C/T | | | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795565 | CTAGCCCAGCCTCAA[C/T]TTCCAGGACAGGTGG | 57602 |
rs61588189 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP36 | GRCh38.p7 | 17:78806688 | GATCTTCCACCTACT[A/G]TGAAAACAGGGAACT | 57602 |
rs61651919 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP36 | GRCh38.p7 | 17:78805874 | TCAGTCCCCAGCACA[C/T]CACATCACCACAAGG | 57602 |
rs61729065 | snp | A/G | 0.00577557 | 0.0534269 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821039 | GTAGGTGTCCGAGAC[A/G]CTCTTGCACACGGAG | 57602 |
rs61737840 | snp | A/G | 0.00561437 | 0.0526846 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835332 | TAGAGGTGGTGTGTA[A/G]GTCAAGCACTGGATG | 57602 |
rs61757572 | snp | C/T | 0.0219852 | 0.102521 | intron-variant | USP36 | GRCh38.p7 | 17:78812853 | CCTCCATCATTCTCA[C/T]AAATACCTTTCCAGT | 57602 |
rs61760231 | snp | C/G/T | 0.00937502 | 0.0678346 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803535 | GTGCCATCTTCCTGC[C/G/T]GTCTGACAGCGGGCA | 57602 |
rs62075586 | snp | C/T | 0.485255 | 0.0845871 | intron-variant | USP36 | GRCh38.p7 | 17:78791803 | TCTTGCCTTAAAAGA[C/T]TGTCCTGGAGGCCAG | 57602 |
rs62075587 | snp | C/T | 0.444133 | 0.157519 | intron-variant | USP36 | GRCh38.p7 | 17:78793804 | ATAAACAGATGCCCA[C/T]CTGATTCCCCAGTGT | 57602 |
rs62075588 | snp | C/T | 0.0490859 | 0.148773 | intron-variant | USP36 | GRCh38.p7 | 17:78806334 | GTCTAAAAAAGGTTT[C/T]CGTGAGTGAAGAGGG | 57602 |
rs62075624 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | USP36 | GRCh38.p7 | 17:78813630 | AAAAGTGTCCTTCCC[C/T]GTGGACGGTCTCTAT | 57602 |
rs62075625 | snp | A/G | 0.173643 | 0.238054 | intron-variant | USP36 | GRCh38.p7 | 17:78815007 | TGGGTGTGCAGCAAC[A/G]CTGTGCAGGAGCTCC | 57602 |
rs62075626 | snp | A/G | 0.177182 | 0.23916 | intron-variant | USP36 | GRCh38.p7 | 17:78818318 | TAAATCCATTAAGAC[A/G]GTGGCCCTGGAACTT | 57602 |
rs62075627 | snp | A/G | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78820836 | CTCTAGAAAAAAACA[A/G]GTAAAGACAATGGTC | 57602 |
rs62075628 | snp | A/G | 0.192715 | 0.243348 | intron-variant | USP36 | GRCh38.p7 | 17:78821331 | TCTCCTGCTGAGGGA[A/G]AGCAGAGGGAAGAGC | 57602 |
rs62075629 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78821414 | TATATATATATATAT[A/T]TATATATTTTTTTTT | 57602 |
rs62075630 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78821469 | GTCTTGCTCTGTCAC[C/T]CAGGCTGGAGTGCAG | 57602 |
rs62075631 | snp | C/T | 0.203882 | 0.245709 | intron-variant | USP36 | GRCh38.p7 | 17:78827602 | GAAGAACACCAAGCC[C/T]TCAAAAATGTAAAAT | 57602 |
rs62075632 | snp | A/G | 0.170733 | 0.237101 | intron-variant | USP36 | GRCh38.p7 | 17:78827853 | GGTTGAGGCTGCAGT[A/G]AGCTATGATCTCACC | 57602 |
rs62075634 | snp | A/G | 0.170733 | 0.237101 | intron-variant | USP36 | GRCh38.p7 | 17:78829572 | TCTGAGGGCTATACA[A/G]TCTAGTCACAACTAT | 57602 |
rs62075635 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78831256 | AAAAAAAAAAAAAGG[A/G]ACAACATAAATATTG | 57602 |
rs62075636 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78834997 | AAAAAAATAATATTT[A/G]TATATATATATATAT | 57602 |
rs62075637 | snp | C/G | 0.267908 | 0.249358 | intron-variant | USP36 | GRCh38.p7 | 17:78838759 | TCAGAGCCTGTGGGA[C/G]GGACAGGGAGACCAT | 57602 |
rs66508510 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78831254 | ATATTTATGTTGTCC[-/C]TTTTTTTTTTTTTTT | 57602 |
rs66508511 | snp | A/G | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78831254 | AAAAAAAAAAAAAAA[A/G]GGACAACATAAATAT | 57602 |
rs67569924 | in-del | -/AG | | | intron-variant | USP36 | GRCh38.p7 | 17:78811169 | AGAAACAGTCATCAA[-/AG]GAGGGTCCACCCCAC | 57602 |
rs71360604 | in-del | AA/T | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78804702 | TTAACTTTGCCTTTT[AA/T]AAAAAAAAAAATTTT | 57602 |
rs71365535 | in-del | -/C | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78790590 | GCCACCATGCCTGGC[-/C]TTTTTTGGCTGGTCT | 57602 |
rs71365537 | in-del | -/A | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78804646 | AAAAAAAAAAAAAAA[-/A]AAAAAAAGCAAGCCA | 57602 |
rs71365538 | in-del | -/G | 0.114387 | 0.210022 | intron-variant | USP36 | GRCh38.p7 | 17:78825746 | CCTAAGAGCGCTCCA[-/G]GTGGCTGCACCCTGT | 57602 |
rs71365539 | in-del | -/CACA/CACACA | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836819 | ACACACACACACACA[-/CACA/CACACA]AACGGACACACACAC | 57602 |
rs71385991 | snp | C/T | 0.204803 | 0.245881 | intron-variant | USP36 | GRCh38.p7 | 17:78806073 | CTGTGAGGTTGGCGA[C/T]TCGTCCAACTCCTCA | 57602 |
rs71385992 | snp | C/T | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78831058 | AGTGAAACCCCGTCT[C/T]TACTACAAATACAAA | 57602 |
rs71964596 | in-del | -/TTTTTC | 0.495872 | 0.0452413 | cds-indel, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802479 | CTTTTTTTCTTTTTC[-/TTTTTC]CTTGGAGACTCTTCC | 57602 |
rs72011596 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78804496 | AACAAAAACAAAAAC[-/A]AAAAAAAAAAAACAA | 57602 |
rs72062649 | in-del | -/TG | 0.0310518 | 0.120672 | intron-variant | USP36 | GRCh38.p7 | 17:78788131 | TGAAGCTCTGCAAGT[-/TG]TGTTTAAAATTGCAT | 57602 |
rs72849516 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78793432 | GAAAGCCGAATCCAT[A/G]GCACCCAGATGATCT | 57602 |
rs72849519 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797628 | GCACAGCCTGGCAAA[A/G]ATGTCCAGCAGGTGT | 57602 |
rs72849521 | snp | A/G | 0.100231 | 0.200173 | intron-variant | USP36 | GRCh38.p7 | 17:78808804 | CCCGTTATCTCTCTC[A/G]TTCCCACTGCAGCCC | 57602 |
rs72849522 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78812265 | TGGCACACCTGTCAC[A/G]ACACCTGTAAGTGGT | 57602 |
rs73391008 | snp | C/T | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78829432 | ATATTTTAGGGCTGA[C/T]AGCCCCTTAGTAGTG | 57602 |
rs73391014 | snp | C/T | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78830793 | AAACTCTCCATGAGA[C/T]TGCCTTTACATAAAG | 57602 |
rs73391175 | snp | C/T | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78830941 | TCATTTAAAAGAAAA[C/T]ACAGGCCAGATGCAG | 57602 |
rs73393123 | snp | A/T | 0.123105 | 0.215401 | intron-variant | USP36 | GRCh38.p7 | 17:78838430 | TTTCAGAAGCTTATT[A/T]AAAAAAAAGCATTAT | 57602 |
rs73393127 | snp | A/G | 0.114738 | 0.210248 | intron-variant | USP36 | GRCh38.p7 | 17:78838785 | ACCATCAGTGGAGGC[A/G]ACTCTTCCTGTGCCT | 57602 |
rs73393129 | snp | G/T | 0.123452 | 0.215605 | intron-variant | USP36 | GRCh38.p7 | 17:78838824 | GCTACTTCCCAGGGA[G/T]GCGGCGCGCACCGGG | 57602 |
rs73394904 | snp | A/G | 0.179105 | 0.239737 | intron-variant | USP36 | GRCh38.p7 | 17:78791703 | GCTGAAGAGGCAGGG[A/G]GGATCTGGATCACAA | 57602 |
rs73394911 | snp | C/T | 0.030665 | 0.119967 | intron-variant | USP36 | GRCh38.p7 | 17:78794551 | TGGGACTCTGCCCGC[C/T]GCCTGCGAGACGACG | 57602 |
rs73394914 | snp | A/G | 0.0539704 | 0.155153 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797853 | AGACCGACAGCTCCC[A/G]GGAAGGGACGCCTTG | 57602 |
rs73394916 | snp | A/G | 0.00728935 | 0.0599294 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798504 | AAGTTTCTGGAAGGC[A/G]TTGAAGTTTCTCCTC | 57602 |
rs73394922 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | USP36 | GRCh38.p7 | 17:78799552 | CTTCCCATTCTCAAA[C/G]CCGAGCGATGCCCGC | 57602 |
rs73394926 | snp | C/T | 0.0258865 | 0.110784 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802371 | GATGGTGCGCAGCTG[C/T]TGGACTCGGGGACAA | 57602 |
rs73394943 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | USP36 | GRCh38.p7 | 17:78808846 | TCAAGGGTCTGGTAT[A/G]GAGTCGGTGCTTAAA | 57602 |
rs73394969 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | USP36 | GRCh38.p7 | 17:78815917 | ACGCACACATGCATA[C/T]GCACACATACACACA | 57602 |
rs73394977 | snp | A/T | 0.0966517 | 0.197444 | intron-variant | USP36 | GRCh38.p7 | 17:78816943 | TATTCACTGTTCTGA[A/T]TTCTGTCACCATTAA | 57602 |
rs73394987 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | USP36 | GRCh38.p7 | 17:78819803 | TTTTTAGGACACACA[C/T]AGGTTCCTCAAGAAA | 57602 |
rs73394990 | snp | C/T | 0.0156258 | 0.0869985 | intron-variant | USP36 | GRCh38.p7 | 17:78819888 | AGGGGACTTATTTCC[C/T]GTCTGGTATCAGTCT | 57602 |
rs73407927 | snp | A/G | 0.148661 | 0.22854 | intron-variant | USP36 | GRCh38.p7 | 17:78822717 | TACTCACGCTGGAAG[A/G]TTCTGAAACAATACA | 57602 |
rs73407930 | snp | C/T | 0.135143 | 0.222054 | intron-variant | USP36 | GRCh38.p7 | 17:78823055 | CCCGCAGGCTACACT[C/T]CCCCTCCCACAGAAC | 57602 |
rs73407932 | snp | A/C | 0.0798611 | 0.183174 | intron-variant | USP36 | GRCh38.p7 | 17:78823068 | CTTCCCCTCCCACAG[A/C]ACATGCACACCTCAG | 57602 |
rs73407940 | snp | C/T | 0.030278 | 0.119257 | intron-variant | USP36 | GRCh38.p7 | 17:78825446 | TTCACTACAGACCAG[C/T]GAAAGCTCCCTCATG | 57602 |
rs73407969 | snp | C/T | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78828452 | AGCTCTCCCTCAGGC[C/T]CACCTGCCTGCCCCA | 57602 |
rs74001239 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | USP36 | GRCh38.p7 | 17:78788008 | AGCCCTGAGGACACC[G/T]TGATTCCAGACTCTG | 57602 |
rs74001242 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78791435 | TGGCCTTCTTTTTAT[A/G]GGAAGTCATGATTCA | 57602 |
rs74001246 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78793285 | GTGGGCACATATGCA[A/G]TGAGAGAGCAAAATA | 57602 |
rs74001247 | snp | C/G | 0.00716266 | 0.059414 | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795648 | ACCAACAAAGACACA[C/G]AACTCACAAAACCGG | 57602 |
rs74001248 | snp | C/T | 0.0626037 | 0.165477 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797029 | CCACTATTTGCATAT[C/T]TGGGAAAGGAAACAT | 57602 |
rs74001249 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797302 | TACTCACAAGGAAGG[A/G]GTGCACAGTAGGGCC | 57602 |
rs74001250 | snp | C/T | 0.0383715 | 0.133092 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797665 | ACCTCTGCTCACACA[C/T]ACACTGTCGTTTCTC | 57602 |
rs74001252 | snp | A/G | 0.00272122 | 0.0367859 | intron-variant | USP36 | GRCh38.p7 | 17:78798866 | GAGCTGAGCCACGCC[A/G]CCCTGCTCCCTCAAG | 57602 |
rs74001255 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | USP36 | GRCh38.p7 | 17:78799205 | TGTGGTCGGTCAGCA[C/T]GGAACCCCCAGCGAT | 57602 |
rs74001256 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP36 | GRCh38.p7 | 17:78799277 | TTCTTTCTAAACCCA[C/T]GCCCTCGTCTGAGGA | 57602 |
rs74001257 | snp | C/T | 0.128632 | 0.218563 | intron-variant | USP36 | GRCh38.p7 | 17:78799613 | TCCACACCCTTCCCT[C/T]CTACAAAACCAACCA | 57602 |
rs74001264 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP36 | GRCh38.p7 | 17:78809618 | GAGTTCCTGTGGCAA[A/G]TGGGGCTTCCTTTGT | 57602 |
rs74001266 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | USP36 | GRCh38.p7 | 17:78813645 | TGTGGACGGTCTCTA[A/T]GACACATGACAAATC | 57602 |
rs74001269 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78818499 | CTTCCCGTCCTGGAC[A/G]AGGGCGAAACTACAG | 57602 |
rs74001272 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | USP36 | GRCh38.p7 | 17:78822658 | TTCTCACCCGGACCC[A/G]GGGCTGCCTGGCGCC | 57602 |
rs74001276 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | USP36 | GRCh38.p7 | 17:78822720 | TCACGCTGGAAGGTT[C/G]TGAAACAATACACCA | 57602 |
rs74001280 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78824410 | GGCGTATGAAACCAG[C/G]AGGCAGCATGGAGCG | 57602 |
rs74001283 | snp | A/G | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78828620 | GCTGTTAGCACAGAG[A/G]GATTCCCAAGACTTC | 57602 |
rs74001287 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78830330 | TCCATGTTGCTAGAC[A/G]TAGCTCCAGTTCCTT | 57602 |
rs74001291 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP36 | GRCh38.p7 | 17:78832236 | AGACAGTCCAGCCTA[C/T]GGCAGGAGCTGCTGC | 57602 |
rs74001296 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP36 | GRCh38.p7 | 17:78835539 | AAGAAAAGAGGAAGA[C/T]GTAAGTCCACACACA | 57602 |
rs74001297 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | USP36 | GRCh38.p7 | 17:78839122 | AACCTCAGGGAGTAA[C/T]AGGAGTTGCCAAAAT | 57602 |
rs74001298 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78839808 | CACTAGCAATCCCTC[C/G]GACGCACACACCATC | 57602 |
rs74001299 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841431 | CCGAGGAAATGGCTC[G/T]TCGGAATTAGGGATC | 57602 |
rs74256159 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | USP36 | GRCh38.p7 | 17:78815395 | GTGAGTCTTCTCCAG[C/T]CAGCCTATGGGAAAC | 57602 |
rs74336551 | snp | A/G | 0.0333695 | 0.124785 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796408 | GAACATTCAGAGACT[A/G]GTCCGCAGGAGAGGG | 57602 |
rs74363680 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78813303 | CACACTCTGCAGAGA[C/T]GTACAAAGCAGCAAA | 57602 |
rs74620083 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811018 | ACTCAGGAGGCAGAG[C/G]CAGGAGAATCGCTTG | 57602 |
rs74725827 | snp | A/G | 0.0134861 | 0.0810011 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797063 | GCTAATGGAAGCCAC[A/G]GGACTGGTCAAAAAT | 57602 |
rs74752375 | snp | A/G | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78804847 | AACAATAAATGGTAA[A/G]GAAAAAAAAGATCCC | 57602 |
rs74763131 | snp | A/C | 0.0501905 | 0.150254 | intron-variant | USP36 | GRCh38.p7 | 17:78804944 | GGAAAGCAAGTGTTG[A/C]GCTGGCCTAATGACA | 57602 |
rs74815092 | snp | A/G | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78831961 | AAAAAAAAAAAAAAA[A/G]AGCTTCTTTCAGCCT | 57602 |
rs74833171 | snp | C/T | 0.046775 | 0.145601 | intron-variant | USP36 | GRCh38.p7 | 17:78821857 | AAGAAAGAGCCCCAG[C/T]CTGCGTTCCAACTCT | 57602 |
rs74980201 | snp | A/G | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78791235 | CACCTCCCGGGTTCA[A/G]GCGATTCTCCTGCCT | 57602 |
rs75080886 | in-del | -/C | 0.442113 | 0.159977 | intron-variant | USP36 | GRCh38.p7 | 17:78833833 | CCATTTTCTTTCTCG[-/C]CATTTTCCTTATTAT | 57602 |
rs75130659 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | USP36 | GRCh38.p7 | 17:78811394 | ATGACTATGTACGTA[A/T]GCATATACACATATT | 57602 |
rs75241026 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | USP36 | GRCh38.p7 | 17:78805786 | CTCACTCAAGCCTCT[C/T]GCCAAGGCCTCACTT | 57602 |
rs75288702 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832751 | CCAAAACCATGAGAC[A/G]AAAACAACAGCCATC | 57602 |
rs75321857 | snp | A/G | 0.0029611 | 0.0383638 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812938 | CACACTCGGGCGGCC[A/G]GGAAGGGAGGAGGAG | 57602 |
rs75402140 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78800133 | ACAAAAAGCTAAAAA[A/C]CAAAAAAAAAAAAAC | 57602 |
rs75462245 | snp | C/G | 0.0209618 | 0.100207 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799723 | TCCTGGACCACATCA[C/G]ACTCCCGCTCTCCAT | 57602 |
rs75648773 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | USP36 | GRCh38.p7 | 17:78812375 | TTTCTCTATAGCCAA[C/T]GTCAGCTGATGACCA | 57602 |
rs75784291 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78827978 | CCTGTAATCCCAACA[A/C/T]TTTGGAAGGCCAAGG | 57602 |
rs75855154 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | USP36 | GRCh38.p7 | 17:78809556 | TGTGCCTGACACAGG[A/G]ACTCTCCTTGAGCCA | 57602 |
rs75908905 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | USP36 | GRCh38.p7 | 17:78800841 | GCACTTCAGTAGACA[A/C]AACCAGCACCTGGCA | 57602 |
rs75961490 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | USP36 | GRCh38.p7 | 17:78815838 | GCACACATATATACA[C/T]ACACACACACATATG | 57602 |
rs75975389 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802479 | CTTTTTTTCTTTTTC[C/T]TTTTCCTTGGAGACT | 57602 |
rs76011270 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78808179 | TCCAAATGGTTCTGG[A/C]CTGAAGAGTTGCATC | 57602 |
rs76042381 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816452 | CCAACATGGTGGAAC[C/T]CCGTCTCTACTAAAA | 57602 |
rs76141906 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78808295 | TTGCCCAGGCTGGAG[A/T]GCAGTGGCATGATGA | 57602 |
rs76177183 | snp | A/G | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78811885 | AGAAAAAAAAAAAAG[A/G]ATATTTTTTCCTACA | 57602 |
rs76208340 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78807826 | TGGTGTTCTGTGACA[C/T]CCCAAGAACAGGGAC | 57602 |
rs76302601 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | USP36 | GRCh38.p7 | 17:78838116 | CAAAAAAAATCGTGG[C/T]TCACGCCTGTAATCC | 57602 |
rs76330038 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | USP36 | GRCh38.p7 | 17:78809242 | CATAATTCTTCTACA[C/T]TTTATCCTTCAACTT | 57602 |
rs76398905 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802251 | CCCCTCGCCCGGTGC[A/G]CACCCATGCGGTCCC | 57602 |
rs76569259 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78820256 | GGGGCAGGAGGATCA[C/T]TGAGGCCAGGAGTTT | 57602 |
rs76579735 | snp | A/G | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78804849 | CAATAAATGGTAAGG[A/G]AAAAAAAGATCCCGT | 57602 |
rs76822769 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78817482 | GACATCTACTGGGCA[C/T]GGTGGCTCATGCCTG | 57602 |
rs76852804 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | USP36 | GRCh38.p7 | 17:78834961 | ATTCCAGCCTGGGTG[C/T]CAGAGCAAGATACTG | 57602 |
rs76853079 | snp | C/T | 0.154329 | 0.23097 | intron-variant | USP36 | GRCh38.p7 | 17:78815850 | ACATACACACACACA[C/T]ATGCATGCATACACA | 57602 |
rs76880523 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836820 | ACACACACACACACA[A/C]ACGGACACACACACA | 57602 |
rs76991945 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78839809 | ACTAGCAATCCCTCC[A/G]ACGCACACACCATCC | 57602 |
rs77044116 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78839601 | GGGAGATGTAACCCA[C/G]TTTCACTCGAGATAA | 57602 |
rs77095877 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78794328 | AACCCTTCTTGTCCA[A/T]ACTGTCAAACAAAAC | 57602 |
rs77203712 | snp | A/C/G | 0.0115166 | 0.0750268 | intron-variant | USP36 | GRCh38.p7 | 17:78838889 | TCCACGCGTGCACTC[A/C/G]GGATGAGGCGGGTGG | 57602 |
rs77261246 | snp | C/T | 0.0140998 | 0.0827712 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802378 | CGCAGCTGCTGGACT[C/T]GGGGACAACAGCATC | 57602 |
rs77292004 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78817187 | TAGGAGCAATGGGCT[A/G]TACCATACAGCTGGC | 57602 |
rs77302552 | snp | A/G | 0.00785297 | 0.0621677 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802353 | GGACACCAGCCATTC[A/G]CGGATGGTGCGCAGC | 57602 |
rs77517092 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78802250 | ACCCCTCGCCCGGTG[C/T]ACACCCATGCGGTCC | 57602 |
rs77861957 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | USP36 | GRCh38.p7 | 17:78816950 | TGTTCTGATTTCTGT[C/T]ACCATTAATTTTGCC | 57602 |
rs77865958 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78809656 | GGGTTTTTTGAGACA[A/G]GGTCTCATTCTGTTG | 57602 |
rs77866879 | snp | C/T | 0.00716266 | 0.059414 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787129 | TACACGCACGCGCTA[C/T]CACGCCCTGCTAATT | 57602 |
rs78113812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78830265 | CCAAACTTCCTTTCT[A/G]TAAATCGTATCATGC | 57602 |
rs78126166 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | USP36 | GRCh38.p7 | 17:78820740 | AGCCCTGGGGACAGC[A/G]TTGTTCCTGTTCATG | 57602 |
rs78335284 | snp | A/G | 0.029116 | 0.117091 | intron-variant | USP36 | GRCh38.p7 | 17:78793747 | TAAACTGCCCTTAAG[A/G]TCACTATTACAGTTA | 57602 |
rs78417383 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78827976 | TGCCTGTAATCCCAA[C/G]ACTTTGGAAGGCCAA | 57602 |
rs78427445 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78788561 | AGCTTCCAGAAGGTG[C/G]AAGCTGGAGGGTCTC | 57602 |
rs78492260 | in-del | -/AAA | | | intron-variant | USP36 | GRCh38.p7 | 17:78795027 | AAAAAAAAAAAAAAA[-/AAA]GTAAAAACCACAGCC | 57602 |
rs78570215 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP36 | GRCh38.p7 | 17:78812140 | TGCCCTGAACCATGA[C/T]TGTGCCACTGTACTC | 57602 |
rs78586109 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | USP36 | GRCh38.p7 | 17:78809392 | ATCTTTCCACTGCAC[C/T]GCAAAGCCGTTTCAC | 57602 |
rs78592046 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | USP36 | GRCh38.p7 | 17:78825137 | AAACTGCATCATCAG[G/T]AGACCCATCCATGGA | 57602 |
rs78602598 | in-del | -/CGATAACTCTCAATAAATA | 0.175897 | 0.238765 | intron-variant | USP36 | GRCh38.p7 | 17:78808237 | AAGCATTTTTATGGG[-/CGATAACTCTCAATAAATA]TCTTTAAGACAGAGC | 57602 |
rs78646319 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | USP36 | GRCh38.p7 | 17:78808210 | CCAGTTTTATCTTAA[A/G]GCTATTATCTCAAGC | 57602 |
rs78771345 | snp | A/C/G | 0.0444908 | 0.142359 | intron-variant | USP36 | GRCh38.p7 | 17:78829679 | TTACACACACAGAGA[A/C/G]CAGGCCAGATGAGTC | 57602 |
rs78872473 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP36 | GRCh38.p7 | 17:78835058 | TTCTGTCTGGGTAAT[C/T]ATTTACAGAAAAGCT | 57602 |
rs78902408 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78832697 | GGCAGCTCTACAGTG[G/T]AAGAGCCCTGACAGG | 57602 |
rs78991885 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837962 | CAGTGGCCTGGGCCT[C/G]TCGTCCCAGATGCTT | 57602 |
rs79112051 | snp | A/T | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78816157 | GAAAAACATACGCAT[A/T]ATTTTTTTTTTTTTT | 57602 |
rs79164046 | snp | A/T | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78816159 | AAAACATACGCATAA[A/T]TTTTTTTTTTTTTTT | 57602 |
rs79204268 | snp | C/T | 0.129664 | 0.219133 | intron-variant | USP36 | GRCh38.p7 | 17:78806059 | ATGCTTTGTCTGTCC[C/T]GTGAGGTTGGCGATT | 57602 |
rs79372583 | snp | A/G | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78811883 | AAAGAAAAAAAAAAA[A/G]GGATATTTTTTCCTA | 57602 |
rs79510368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816752 | TAAGTGCTGACATTA[C/G]AGTTGTGAGCCATTG | 57602 |
rs79569725 | snp | A/C | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78838371 | AGCAAGACTTGGTCT[A/C]AAAAAAAAAAAAAAA | 57602 |
rs79628244 | snp | C/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795665 | ACTCACAAAACCGGA[C/G]TATTTTATTGCACCA | 57602 |
rs79704391 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78823597 | CACCCGGAATCACAG[C/T]TGCAAAGGGCACCCT | 57602 |
rs79833420 | snp | A/C | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78833878 | TAGGAACTTTATAGA[A/C]TGAGCTGGGAAAGAT | 57602 |
rs79941976 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816451 | GCCAACATGGTGGAA[C/T]CCCGTCTCTACTAAA | 57602 |
rs79953196 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78824709 | AATTGAGACCAAACT[C/T]TTCAGTCATAACAGG | 57602 |
rs79959144 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | USP36 | GRCh38.p7 | 17:78816823 | TTGTTGAAATGCATA[A/G]ATCTTCAGTATATAG | 57602 |
rs80052933 | in-del | -/AA | | | intron-variant | USP36 | GRCh38.p7 | 17:78811882 | CAAAGAAAAAAAAAA[-/AA]GGATATTTTTTCCTA | 57602 |
rs80312300 | snp | A/C | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78838372 | GCAAGACTTGGTCTC[A/C]AAAAAAAAAAAAAAC | 57602 |
rs111298702 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78833085 | CACAGGAGGCGGGGG[C/T]TGCAGTGAGCCGAGA | 57602 |
rs111318763 | snp | A/G | 3.32502e-05 | 0.00407725 | intron-variant | USP36 | GRCh38.p7 | 17:78799777 | CTCAGCCCTGCAATC[A/G]GAGCAGCCAAGAAAC | 57602 |
rs111340845 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP36 | GRCh38.p7 | 17:78830181 | AATTAGGCAATTATC[A/G]TTCTCATTCATGTAT | 57602 |
rs111370500 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78802717 | ACGCAGCCACGGAGA[C/T]AGTAGAGGGAAAACC | 57602 |
rs111390283 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78819307 | GATATTCAGCCGGCT[C/G]TAGTAGTGTGATCCC | 57602 |
rs111519790 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78811639 | CTTTGGGAGGCTGAG[A/G]CGGGTGGATCAGGAG | 57602 |
rs111544658 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | USP36 | GRCh38.p7 | 17:78830387 | TGAATGAAGAGACCA[C/G]TGTTATTTATGTATC | 57602 |
rs111673036 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78816661 | CAAAATTTTTTTGTA[A/G]AGACAGGGTCTCACT | 57602 |
rs111682734 | snp | C/T | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78821356 | AAGAGCTGCCTCCTC[C/T]CTGCACGCGTGCACG | 57602 |
rs111709949 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | USP36 | GRCh38.p7 | 17:78793008 | GGTGTGAGCCACCGC[A/G]CCCGCCCCCCTCACC | 57602 |
rs111779104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833660 | TGTGTTTTCAACTGC[C/T]CTGCTCCCTCCAGAA | 57602 |
rs111805955 | snp | C/T | 0.109461 | 0.206758 | intron-variant | USP36 | GRCh38.p7 | 17:78833304 | TATGTTTTTTTGAGA[C/T]GGAATCTTGTTCTGT | 57602 |
rs111817223 | in-del | -/CACACCC | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78798131 | CAGATGCCAGGTGTA[-/CACACCC]CACACCCAACACACA | 57602 |
rs111838345 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | USP36 | GRCh38.p7 | 17:78801241 | TCGGCCTCCCAAAGT[A/G]TTGGGATTACAGGCG | 57602 |
rs111864724 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819550 | GCACAGTCCCTGGGG[C/T]GGCCGCCCGGTGCCA | 57602 |
rs112045226 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP36 | GRCh38.p7 | 17:78812652 | CCGAGATTGGAGATC[A/G]CACCACTGCACCCCA | 57602 |
rs112053931 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837115 | TTGAGTTAAATAAAT[C/T]ATGAAAATGAATTTC | 57602 |
rs112162421 | snp | C/T | 0.172028 | 0.23753 | intron-variant | USP36 | GRCh38.p7 | 17:78834928 | CAAGACTACAACGAG[C/T]TGTGATGGAGCCACT | 57602 |
rs112211361 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842894 | TTTTAGGATTTAGAG[A/G]TCATTCAGTCTCATC | 57602 |
rs112234844 | snp | C/T | 0.000132181 | 0.00812854 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803591 | CATGGGGCTCCCAGG[C/T]TGTCTCTGTGTCTGC | 57602 |
rs112248406 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78788542 | TGGGGCAGTGGGGGT[A/G]CCCAGCTTCCAGAAG | 57602 |
rs112349667 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | USP36 | GRCh38.p7 | 17:78815956 | CACATGCATGCACAC[A/G]CATATACATACACAC | 57602 |
rs112360629 | in-del | -/T | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78788172 | TATTTTATTTATTTA[-/T]TTTTTTTTTTTGAGA | 57602 |
rs112464815 | snp | A/C | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78835203 | GACCCAGACTGAGAG[A/C]AGCAGTGCCACAAGT | 57602 |
rs112469762 | snp | A/G | 0.00245901 | 0.0349779 | intron-variant | USP36 | GRCh38.p7 | 17:78813732 | GTATAAGAAAAGAGC[A/G]GAGGGAGTGAGCTCA | 57602 |
rs112525474 | snp | C/T | 0.000209386 | 0.0102298 | intron-variant | USP36 | GRCh38.p7 | 17:78829029 | GCGTGGAAGGAGGAG[C/T]AATTTTAAGACAAGA | 57602 |
rs112622238 | snp | A/G | 0.135484 | 0.22223 | intron-variant | USP36 | GRCh38.p7 | 17:78821658 | GGCCAGGCTGGCCTC[A/G]AACTCCTGACCTCAG | 57602 |
rs112631530 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836796 | CTGGTTATACACACA[C/T]GGACACACACACACA | 57602 |
rs112659657 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | USP36 | GRCh38.p7 | 17:78788207 | GCCTCACTCTGTCGC[C/G]AGGCTGGAGCGCAGT | 57602 |
rs112711505 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78794019 | CTACTACTTGGCCTC[C/T]GAACCCAACTAACCA | 57602 |
rs112779098 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78805702 | GGAACCCGAGAGCCC[C/T]GAGACAGTTCTTAAC | 57602 |
rs112790707 | snp | C/G/T | 4.95089e-05 | 0.00497518 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807401 | AGCCCCTGAGCAGTT[C/G/T]TGGGGGAAAAGTGCT | 57602 |
rs112843316 | snp | C/G/T | 0.000198461 | 0.00995969 | synonymous-codon, missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807153 | GGGCCGCTCCACTCC[C/G/T]GGGGGTCTGGGGGGC | 57602 |
rs112951160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799868 | AACTTACAGTAAGTG[C/G]ATGCTTGCCTTTTTT | 57602 |
rs113000955 | snp | A/G | 0.0287284 | 0.116357 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797695 | CTTGCAGGGCTGGTC[A/G]GGAATGTCACCAAAG | 57602 |
rs113006106 | in-del | -/T | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78790092 | TGGCAGAATAATACC[-/T]TTTTTTTTTTTTTTG | 57602 |
rs113046841 | snp | A/G | 0 | 0 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795677 | GGAGTATTTTATTGC[A/G]CCAAGATCTTGGCAA | 57602 |
rs113130752 | snp | G/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841284 | GGCCGTCAGGTGGCT[G/T]TGGAGAAGCGGAGGC | 57602 |
rs113136795 | snp | A/T | 0.00636936 | 0.0560724 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78786949 | AATATGTTTTTCCTA[A/T]GCTTATACCATGGTT | 57602 |
rs113156875 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | USP36 | GRCh38.p7 | 17:78833422 | AAGTAGCTGGGATTA[C/T]AGGTGTGAGCCACCG | 57602 |
rs113185249 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | USP36 | GRCh38.p7 | 17:78790352 | CTGGAGCACAATGGC[A/G]CGGTCTCAGCTCACT | 57602 |
rs113285510 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842286 | AGAGCGAGACTCCGT[C/T]TCAAAAGAAAAGAAA | 57602 |
rs113337240 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | USP36 | GRCh38.p7 | 17:78788857 | GCCAGAGGTGGGGAC[A/G]GGAGGGACACTGAGG | 57602 |
rs113341332 | snp | A/G | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78827942 | AAGAATGTAAAATCC[A/G]GCAGGATGCAATGGC | 57602 |
rs113361080 | snp | C/T | 0.132751 | 0.2208 | intron-variant | USP36 | GRCh38.p7 | 17:78831157 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 57602 |
rs113586045 | snp | A/C | 0.0142736 | 0.0832652 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797510 | CTATGCACCGGGAGA[A/C]CACCTGGGGGACATG | 57602 |
rs113602007 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | USP36 | GRCh38.p7 | 17:78794252 | GCCGCCTTTCAGGCC[A/T]TCAGGCAGCCTGGAA | 57602 |
rs113629302 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788180 | TTTATTTATTTTTTT[C/T]TTTGAGACAGAGCCT | 57602 |
rs113650447 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78840284 | GGAACCGCACCCCGC[C/G]CCGGGCTCCATGGCC | 57602 |
rs113660376 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842144 | ACATACAAAAATTAG[A/C]TGGGTGTGGTGGTGG | 57602 |
rs113671804 | snp | A/C | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78816897 | ATCAACTAGAAAATT[A/C]CCACATCCCAGTCAT | 57602 |
rs113744168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78798249 | CACACACCACAGACG[C/T]GCCCACACCACACAC | 57602 |
rs113781422 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP36 | GRCh38.p7 | 17:78838848 | CACCGGGAACCCTCT[A/G]CCACGAAAAAGCCGT | 57602 |
rs113839382 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78832881 | CTGCAGGGCACGGTG[A/G]CTCATGCCTGTAATC | 57602 |
rs113889989 | in-del | -/CT | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78823356 | CCACCCCCACAACCC[-/CT]CTGTCATCCAGAAGC | 57602 |
rs113942129 | snp | C/T | 0.077417 | 0.180873 | intron-variant | USP36 | GRCh38.p7 | 17:78812406 | GTTTAAGAAATAACA[C/T]TGGCCGGGCGCGGTG | 57602 |
rs113954300 | snp | C/T | 0.134802 | 0.221877 | intron-variant | USP36 | GRCh38.p7 | 17:78821576 | GGGATTGCAGGCATG[C/T]GCCACCGCGCCTGGC | 57602 |
rs113993737 | snp | A/G | 0.030665 | 0.119967 | intron-variant | USP36 | GRCh38.p7 | 17:78815062 | ATGCTGGCCAGGTGC[A/G]GTGGCTCACGCCTGT | 57602 |
rs114100446 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78790669 | TGGAATTACAAGCAT[A/G]AGCCACTGCGCCCGG | 57602 |
rs114124275 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78810738 | TAAATGACCAAAACC[A/C]CTGCAGACTGTGAAA | 57602 |
rs114167365 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78823056 | CCGCAGGCTACACTT[C/T]CCCTCCCACAGAACA | 57602 |
rs114243243 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78802967 | TTTTTTTTAGACAGG[C/G]TTTAGCTGTCACCCA | 57602 |
rs114270897 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837788 | GCCCTCAGAGAATCA[A/G]CAAGTCAAGTGTGCC | 57602 |
rs114280214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78834604 | GGTGCACCCCATCAC[A/G]CCTAATTTTTATATT | 57602 |
rs114461079 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | USP36 | GRCh38.p7 | 17:78809756 | AACCTCCAAACAGCT[A/G]GGACAACAGACGTGC | 57602 |
rs114473472 | snp | A/G | 0.00336079 | 0.0408546 | intron-variant | USP36 | GRCh38.p7 | 17:78827220 | GTGTCCAAAGCCCTG[A/G]GAGGGTGGGTGGGGA | 57602 |
rs114691947 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | USP36 | GRCh38.p7 | 17:78806092 | TCCAACTCCTCACCA[A/G]CCAAGCACACGCAAC | 57602 |
rs114693790 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78822963 | CCCAGCTGCTTCCCC[A/G]ACTCCTCACTGGCAC | 57602 |
rs114712966 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836907 | CAGACCTGCACTCTT[C/T]AATATGAAGGCCACA | 57602 |
rs114713166 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78805418 | GAGGCTGTGGGCGAC[A/G]CACAGTCATACCTCG | 57602 |
rs114894053 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78824414 | TATGAAACCAGCAGG[A/C]AGCATGGAGCGTGCC | 57602 |
rs114905121 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | USP36 | GRCh38.p7 | 17:78803314 | GACCATACCTACTTG[C/G]GGGTAGATTCTGTGG | 57602 |
rs114907107 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78792420 | GTCCCCACAGAGGAT[A/G]GGGAACAGCCCCTAT | 57602 |
rs114959181 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78813296 | CCTCAGCCACACTCT[A/G]CAGAGACGTACAAAG | 57602 |
rs114987270 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78819117 | GCTGAGTGATAAAAC[A/G]GGCAGGCAGGAAGTC | 57602 |
rs115029701 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78809833 | TTGGAGATGGGGGTC[A/T]TTCTATGTTGCCCAG | 57602 |
rs115036891 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | USP36 | GRCh38.p7 | 17:78815795 | ACACATATATACATA[A/C]ATGCATACATACATC | 57602 |
rs115042629 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | USP36 | GRCh38.p7 | 17:78827646 | GGTGGCTCACACCTG[C/T]CACTCTAACACTTCA | 57602 |
rs115083683 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | USP36 | GRCh38.p7 | 17:78825517 | CCTGGCCACCTGACA[C/G]CTGGCCTCCCTCCTC | 57602 |
rs115200170 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP36 | GRCh38.p7 | 17:78802737 | GAGGGAAAACCAGTC[A/G]CGTTTCCCATCCTAA | 57602 |
rs115477327 | snp | A/G | 0.00263437 | 0.0361973 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814475 | CACCAGGACAGCATA[A/G]AGTCCATACATGACA | 57602 |
rs115501663 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78815796 | CACATATATACATAC[A/G]TGCATACATACATCG | 57602 |
rs115656714 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78822595 | TCATTCATGTCCCCC[A/G]CACCGCTCACTAACT | 57602 |
rs115746476 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP36 | GRCh38.p7 | 17:78800738 | CACAGGACTGCAAGA[A/G]CCCATGCGGCCCCCA | 57602 |
rs115853169 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78813369 | CAGTGACAGCCAGCT[C/G]CAGGAGAAGGCCCCT | 57602 |
rs115856516 | snp | C/T | 0.0235261 | 0.105875 | intron-variant, synonymous-codon | USP36 | GRCh38.p7 | 17:78823163 | CTTGGGGGACCAATA[C/T]AGGATCATTCAATTT | 57602 |
rs115923305 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797504 | CACCAGCTATGCACC[A/G]GGAGACCACCTGGGG | 57602 |
rs115969510 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78804972 | ACACCTCCACATTAC[C/T]GTCATTAGGACGCTG | 57602 |
rs116034148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824660 | ACAGTAAATATGCTA[C/T]CTATAATTACTATAA | 57602 |
rs116069648 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | USP36 | GRCh38.p7 | 17:78808991 | ATGCAAAATGCCAAA[A/C]TGCTTTTACTATACT | 57602 |
rs116245487 | snp | G/T | 0.00585574 | 0.053792 | intron-variant | USP36 | GRCh38.p7 | 17:78814396 | GGAGGCAGCTGCACT[G/T]ACACAAGCCTCTCAC | 57602 |
rs116276318 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836844 | ACACACACACACCCA[C/T]GCAATAAATGAATTA | 57602 |
rs116283213 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP36 | GRCh38.p7 | 17:78792385 | CAGAGGGGGCACCTC[A/G]TCCAGCATCTCCAGT | 57602 |
rs116283596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823224 | AACTGCCACCATCTA[C/T]TGTCCCACCATTCTT | 57602 |
rs116298355 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78835607 | AGCATGCAGTGACTC[A/G]GAACATGGCACCAGA | 57602 |
rs116299579 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78829672 | ACTTTATTTACACAC[A/C]CAGAGAGCAGGCCAG | 57602 |
rs116447647 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797436 | AGGGGAGGGCGGGCT[C/T]GGACACAACGGTGGC | 57602 |
rs116463176 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | USP36 | GRCh38.p7 | 17:78834945 | GTGATGGAGCCACTG[A/C]ATTCCAGCCTGGGTG | 57602 |
rs116643275 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78809563 | GACACAGGGACTCTC[C/T]TTGAGCCAATCTCCA | 57602 |
rs116699838 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | USP36 | GRCh38.p7 | 17:78807906 | ATGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 57602 |
rs116919093 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | USP36 | GRCh38.p7 | 17:78830171 | CACTATCCTGAATTA[A/G]GCAATTATCGTTCTC | 57602 |
rs116930035 | snp | G/T | 0.0539704 | 0.155153 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837974 | CCTGTCGTCCCAGAT[G/T]CTTGGGAGGCTGAGG | 57602 |
rs116935963 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78794490 | ATGGCCTCCCTGCAT[C/G]TCCCTAACAGCACTC | 57602 |
rs116980189 | snp | C/T | 0.0225045 | 0.103662 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796923 | TAAGTTACAAGTTGG[C/T]AGGCACAGCTTGAGC | 57602 |
rs117093243 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | USP36 | GRCh38.p7 | 17:78798726 | CCCCTATTGACAAAG[A/G]GGCGGAAGCTGCGAG | 57602 |
rs117203268 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78818489 | CTGTGACTGTCTTCC[C/T]GTCCTGGACAAGGGC | 57602 |
rs117259737 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP36 | GRCh38.p7 | 17:78806821 | CAAATGGCTGGGAAC[A/G]ACTAAAAGACACTTT | 57602 |
rs117313714 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78824015 | AGAAAACAGACATGA[G/T]GCCAAGGACACAGCC | 57602 |
rs117389925 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP36 | GRCh38.p7 | 17:78820467 | GACCCTGTCCCTCAA[A/G]CCCCTATAAAAAAAA | 57602 |
rs117433267 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78798351 | CCTACACACATACAC[A/G]GCACACACACCCCCA | 57602 |
rs117475713 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797188 | AGCTACAGCACAGTC[A/G]TCTCAGAATAAACAG | 57602 |
rs117541464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792330 | GTCCCCAGGGTGGAA[A/G]AAGTTGGCCTCAAGG | 57602 |
rs117549034 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP36 | GRCh38.p7 | 17:78830334 | TGTTGCTAGACATAG[C/T]TCCAGTTCCTTCAAA | 57602 |
rs117644066 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | USP36 | GRCh38.p7 | 17:78831512 | CAGCTACTTGGGAGG[A/G]TGAGGGAAGAGAATC | 57602 |
rs117681764 | snp | A/G | 0.0130921 | 0.0798413 | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795642 | AATGAAACCAACAAA[A/G]ACACAGAACTCACAA | 57602 |
rs117685712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809542 | AGCGCCCCTGCAGGT[A/G]TGCCTGACACAGGGA | 57602 |
rs117738339 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | USP36 | GRCh38.p7 | 17:78808461 | TTGCTATGTTGCCCC[A/G]GCTAGCCTTGAATTC | 57602 |
rs117840411 | snp | C/T | 0.0119056 | 0.0762322 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812937 | TCACACTCGGGCGGC[C/T]GGGAAGGGAGGAGGA | 57602 |
rs117841914 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | USP36 | GRCh38.p7 | 17:78791743 | GACTATTTTCTCTGA[A/G]CAGGAGTGAGAAACC | 57602 |
rs117885497 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | USP36 | GRCh38.p7 | 17:78799165 | GTGAAGAGAAGGACA[A/C]GAGGAGGACGGCTCG | 57602 |
rs117897648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78815871 | TGCATACACATGTAC[A/G]CATATACATACATGC | 57602 |
rs117946159 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP36 | GRCh38.p7 | 17:78791865 | TTTGGGAGGCCAAGG[C/T]GAGAAGATTATTTGA | 57602 |
rs118136968 | snp | A/T | 0.0535932 | 0.154675 | intron-variant | USP36 | GRCh38.p7 | 17:78788712 | CTCGGGTCCATGGGG[A/T]AGGTATTGCTGAGGC | 57602 |
rs137858906 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78790444 | TACAGGCGTGTGCCA[C/T]GAGGCCCGGCTAATT | 57602 |
rs137902825 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842220 | CTTGAACCTAGGAGG[C/G]GGAGGTTGCAGCGAG | 57602 |
rs137934093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78812506 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 57602 |
rs137980652 | in-del | -/G | 0.0517044 | 0.152246 | intron-variant | USP36 | GRCh38.p7 | 17:78819154 | GCAAAGCTAGAAGAT[-/G]GCGCAAACACAGGGA | 57602 |
rs137984862 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP36 | GRCh38.p7 | 17:78833101 | TGCAGTGAGCCGAGA[C/T]TGCACCACTGCACTC | 57602 |
rs138013298 | snp | C/T | 0.0364591 | 0.130001 | intron-variant | USP36 | GRCh38.p7 | 17:78835230 | AAGTGCATGGGCTTA[C/T]CTAATCCAGAGGACC | 57602 |
rs138032507 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78794523 | CCTGCCCTGGAGCCG[A/T]CAGTCCTGCCGGTGG | 57602 |
rs138059388 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | USP36 | GRCh38.p7 | 17:78816153 | CTCCGAAAAACATAC[A/G]CATAATTTTTTTTTT | 57602 |
rs138141297 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78824425 | CAGGCAGCATGGAGC[A/G]TGCCTGCAGTTCCAG | 57602 |
rs138145090 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797517 | CCGGGAGACCACCTG[A/G]GGGACATGTGGCCAC | 57602 |
rs138210943 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | USP36 | GRCh38.p7 | 17:78805289 | CAAAAAAGCTTATAA[A/G]GCAAGAAACGAAAAA | 57602 |
rs138324901 | snp | A/C/G/T | 0.000198981 | 0.00997293 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835397 | GGAGTCCTGCGCCCA[A/C/G/T]GCGGAAGACCCGCTC | 57602 |
rs138406149 | snp | C/T | 0.00953873 | 0.0683987 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797634 | CCTGGCAAAGATGTC[C/T]AGCAGGTGTGCGGCC | 57602 |
rs138426339 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | USP36 | GRCh38.p7 | 17:78838829 | TTCCCAGGGATGCGG[C/G]GCGCACCGGGAACCC | 57602 |
rs138440440 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787551 | GCTGAACAAATCTCC[A/G]TTAGGGGCACTGTTC | 57602 |
rs138461758 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP36 | GRCh38.p7 | 17:78830072 | TACCTTTCAAATTAT[A/G]ATGTAAATAAACACT | 57602 |
rs138483624 | snp | C/T | 0.0139609 | 0.0823745 | intron-variant | USP36 | GRCh38.p7 | 17:78802291 | CGCCCGGTGCACACC[C/T]ATGCGGTTCCCACCC | 57602 |
rs138483928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832406 | AAAAAAAGGCCACAA[C/T]GTCTCTTCATATGTT | 57602 |
rs138526951 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78815811 | ATGCATACATACATC[A/G]TATACACACATGCAC | 57602 |
rs138604654 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78790823 | TCTCATGATGGTAAG[A/C]AGCTACCTAAATACC | 57602 |
rs138761721 | snp | A/G | 0.000165011 | 0.00908176 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799677 | AGTACCTTTTCTCCC[A/G]TAAGCTTTATCAGAT | 57602 |
rs138866771 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78818090 | ACCCTGTCTTAAAAC[-/A]AAATGAAATTTAAAC | 57602 |
rs138952849 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78806885 | GACAATGTTCTCACT[C/G]CCTTCAAACCACAAC | 57602 |
rs139009802 | snp | C/T | 0.000658946 | 0.0181394 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813784 | TTACCGCAGATAGAA[C/T]AGCACGTAGGCCTGC | 57602 |
rs139022664 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP36 | GRCh38.p7 | 17:78827721 | CAGCCTGGGTAACAT[A/C]GGGAGACTTCATCTC | 57602 |
rs139098305 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78805947 | AGGACTGCAGAGGCC[A/G]AACTGCCTTCACCAC | 57602 |
rs139133507 | snp | A/G | 0.00184754 | 0.0303374 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807136 | CTGAGAATCGCAGAG[A/G]TGGGCCGCTCCACTC | 57602 |
rs139147825 | snp | C/T | 0.000775348 | 0.0196742 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807635 | GTCCCAGAGTCTTGT[C/T]GCTAAGGAGACCAAA | 57602 |
rs139150225 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78823894 | ATCTTGAAAACCAGC[C/T]GACCCACAAGATAAA | 57602 |
rs139155069 | snp | C/T | 0.000232968 | 0.0107903 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807267 | CCTTCAGCCCATGCC[C/T]GTTGGCAGTGGCTGT | 57602 |
rs139186225 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78835588 | ACTCCTGAAGCATAC[A/G]CTTAGCATGCAGTGA | 57602 |
rs139205429 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78825017 | TAGAGCAAAACTAGA[C/G]GAGATGCAAGGAGAC | 57602 |
rs139221124 | snp | A/G | 0.00100781 | 0.0224252 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814418 | GCCTCTCACCTTCAC[A/G]TAGCAGTAATAGTGC | 57602 |
rs139238049 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78812284 | CCTGTAAGTGGTGCT[C/G]GTCTCATGAGTAGAA | 57602 |
rs139293512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78813628 | TAAAAAGTGTCCTTC[C/T]CTGTGGACGGTCTCT | 57602 |
rs139392617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817010 | TGTGCCACATAACAT[A/G]TTTTGGTCAATGACA | 57602 |
rs139422837 | snp | A/G/T | 0.000182106 | 0.00954069 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807165 | TCCTGGGGGTCTGGG[A/G/T]GGCCTTGGTGGAGTC | 57602 |
rs139437943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78831009 | AGGCAGGTGGATCGC[A/G]AGGTCAGGAGGTTGA | 57602 |
rs139495407 | snp | C/T | 0.000221537 | 0.0105223 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827338 | CCAAAGCGGAAGTGT[C/T]GGGCGATCTCTAAAA | 57602 |
rs139516900 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP36 | GRCh38.p7 | 17:78830664 | AATCATTTCCCCGCA[A/G]TATCTCCAACTCCTT | 57602 |
rs139599952 | snp | C/T | 3.29571e-05 | 0.00405924 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836243 | TGGCTGGCTCGAACT[C/T]GATTTTCTGTAAAAG | 57602 |
rs139624691 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78833696 | CTTAGAGATTTTCTG[A/C]GATGAAAACATCCTG | 57602 |
rs139647599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836554 | CTAATCACTTGGACA[C/T]ATTAGTTCACATTTC | 57602 |
rs139686888 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796509 | TCTAAGAAGAGAAAC[A/G]TAAAAACAGAAGAAA | 57602 |
rs139715778 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78809183 | TTTATTGCTTCATTT[-/G]GTTTGTAGTAAATTA | 57602 |
rs139742855 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP36 | GRCh38.p7 | 17:78798284 | CCCAACACACATGTG[C/T]CAGATACACAGCCCA | 57602 |
rs139745140 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | USP36 | GRCh38.p7 | 17:78789154 | GTGAGTCGAGATTGC[A/G]CCATTGCACCCCAGC | 57602 |
rs139783752 | snp | C/T | 0.00122005 | 0.0246686 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828933 | AGACGGGCTTGATGG[C/T]GTTGCCGCTGTTGGC | 57602 |
rs139827515 | snp | C/T | 0.000350178 | 0.0132275 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807223 | GCTGCTGGAGCCCCT[C/T]CTGTCGAGGCCAGCG | 57602 |
rs139867295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78798826 | GCTTCATGCCACTGC[C/T]GCCACCTCCAACTGC | 57602 |
rs139867786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78821840 | CCCAGGTCTGCACAG[C/T]GAAGAAAGAGCCCCA | 57602 |
rs139874390 | snp | C/G/T | 9.89746e-05 | 0.0070341 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806236 | GTCGGAGGATGGTGA[C/G/T]GGGGGAGGTGGACGG | 57602 |
rs139909760 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78808555 | TGCACCCTGCCTGTC[A/G]GCCTGTCTTTGACAT | 57602 |
rs139956557 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78810479 | TTTTAGTAGAGACAG[A/G]GTTTTGCCCAGGTTG | 57602 |
rs139958921 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78793094 | TACTTCCGTCAGTAT[C/G]GAATGCCTCTCCCCA | 57602 |
rs140036426 | in-del | -/A | 0.172028 | 0.23753 | intron-variant | USP36 | GRCh38.p7 | 17:78819212 | TTGGAGAGCTGCAGG[-/A]AACAGACCTAAAGAA | 57602 |
rs140076085 | snp | A/G | 0.000461156 | 0.0151778 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798922 | CCTTCCCTCGGTCAA[A/G]CTCTTCGTCCCAGTC | 57602 |
rs140142093 | snp | A/C | 0.000276679 | 0.0117585 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802441 | GCCCATCCTCTTCTA[A/C]TGCCCGCTGTGTCTC | 57602 |
rs140156119 | snp | C/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841928 | ATTTATTACCTGGGC[C/G]CTGGTGTTTTTTGAA | 57602 |
rs140224225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78818604 | GGCTATCACTTTCTT[C/T]GTGTTATTCTGATGC | 57602 |
rs140233656 | snp | C/T | 0.02016 | 0.0983543 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78840976 | CTTCCGTGTCGCCTA[C/T]GTCACCTCCCCATCA | 57602 |
rs140272054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790165 | GCGATCTCAGCTCAC[A/T]GCAACCTCGGCTTTC | 57602 |
rs140283267 | snp | A/C/G | 0.0188418 | 0.0952163 | intron-variant | USP36 | GRCh38.p7 | 17:78803996 | GTGGGGACAGCCAGG[A/C/G]AACAGGGAGAGGATG | 57602 |
rs140290111 | snp | A/G | 0.0128008 | 0.0789727 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806170 | CCTGGCTCTATGGAC[A/G]GGCCAAGTGGAGGCA | 57602 |
rs140291695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793647 | CTTTACCACCACGTC[C/T]TTGGCGTACCCACAT | 57602 |
rs140328430 | snp | A/G | 0.00774921 | 0.0617621 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807608 | TCTTCAGTGGTGTGC[A/G]GCTTCTTCATCGTCC | 57602 |
rs140332801 | snp | A/G | 0.000197954 | 0.00994676 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803546 | CTGCCGTCTGACAGC[A/G]GGCAGCTGTGCCTGG | 57602 |
rs140438817 | snp | C/T | 0.000131776 | 0.00811608 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818725 | GAAAGGGTTAAGACG[C/T]TGGATGTTCTGTGGA | 57602 |
rs140440602 | in-del | -/ACAC/ACACAC | 0.316485 | 0.240998 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836798 | GTTATACACACACGG[-/ACAC/ACACAC]ACACACACACACACA | 57602 |
rs140576306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78831296 | TTTTTTTCCAAAACC[C/T]AACTTCAGGTAAGAT | 57602 |
rs140617093 | snp | A/G | 0.000199226 | 0.00997865 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803414 | GTCCTGGTGCAGGCC[A/G]CCTTCTTCACCAAGA | 57602 |
rs140651368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78809530 | CATGGTCAGTGAAGC[A/G]CCCCTGCAGGTGTGC | 57602 |
rs140654133 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835376 | AGCAGGTGTTGCCAA[A/G]GTTGTGGAGTCCTGC | 57602 |
rs140681842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825739 | TTTCTGTCCTAAGAG[C/T]GCTCCAGGTGGCTGC | 57602 |
rs140695347 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP36 | GRCh38.p7 | 17:78816628 | AAGACTCCGTCTCAA[A/G]AAAAAAAACAAAAAA | 57602 |
rs140775990 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78793970 | CCACCTGAAGGCCTT[C/G/T]CTGAAACCATCGGTG | 57602 |
rs140802096 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787573 | GCACTGTTCGTGTGC[C/T]GGGAACACACAGGTC | 57602 |
rs140856412 | snp | C/T | 4.9489e-05 | 0.00497414 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803467 | GCTTCCTGCTGCTCG[C/T]GTGGTGGCCGTCCGT | 57602 |
rs140862933 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78819399 | CAACAAGGTGAAACC[C/G]TGTCACTACTAAAAA | 57602 |
rs140866344 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797150 | CTCAGTGAAGACCTG[A/C]GGGTTATTGCAGCTG | 57602 |
rs140965115 | snp | C/T | 0.00236342 | 0.0342947 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835312 | TTGGAGAGCAGGTAG[C/T]TGGCTAGAGGTGGTG | 57602 |
rs141066245 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78814233 | CACTAGATTCTGGTG[C/T]AACACTTCTGTAAAG | 57602 |
rs141123403 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78834575 | CTTCAGCCTCCCGAG[C/T]AGCTGGGATTACAGG | 57602 |
rs141196869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78806794 | CACCCCAAGATAGCC[A/G]TTCTTTAATTGCAAA | 57602 |
rs141222382 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78832977 | AACATGGTGAAACTT[C/T]GTCTCTACTAAAAAT | 57602 |
rs141280149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808915 | GCTAATTTTCTGGAA[A/G]TGGAATTACAAGGCT | 57602 |
rs141304755 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78794207 | CCTGGCGGCTGGTCA[C/T]GCTCACCTGCTGTTC | 57602 |
rs141354205 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP36 | GRCh38.p7 | 17:78823576 | GGCAGGAGGTGGCCC[A/G]AGAGCCACCCGGAAT | 57602 |
rs141395272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78825934 | TCACAGCATTGGCCA[C/T]ACCACATTGCAAACG | 57602 |
rs141425456 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | USP36 | GRCh38.p7 | 17:78802108 | CCCCACCCCCTTGCC[C/T]GGTGCACACCCACGC | 57602 |
rs141488170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78813446 | CATATCCCTACAGGG[A/G]CAGCTTCCCCACACG | 57602 |
rs141534176 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805741 | CGCTAGCAGGCAAGA[C/T]GTCCCACAAAAAACG | 57602 |
rs141540569 | snp | A/G | 9.88566e-05 | 0.00702983 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813812 | TGCTGGTTCAGAACC[A/G]CCTTGACGTTGCTGG | 57602 |
rs141616643 | snp | A/G | 0.000102608 | 0.00716194 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827310 | CAGGAACTCATGCGC[A/G]TCCTCCTGGTTCCCA | 57602 |
rs141690071 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78826726 | ACATATAAGGGCTTA[C/T]GTGGCGTGTGAATAA | 57602 |
rs141706175 | in-del | -/TC | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78788025 | GATTCCAGACTCTGG[-/TC]TCTCTCTGGCACTGT | 57602 |
rs141802450 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78812684 | CCTGGATGACAGAGC[A/G]AGACTCTGTCTCGAA | 57602 |
rs141805185 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78810230 | CGGGTTCAAGTGATC[C/T]TCCCCCAACAGCTTA | 57602 |
rs141821093 | snp | A/T | 0.000165096 | 0.00908408 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799699 | TTATCAGATGAGTAT[A/T]TGAGCAGTTCCTGGA | 57602 |
rs141861189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78789477 | CAAGCCTCCTGGACT[C/T]GCTAATTTTGCAGCA | 57602 |
rs141872352 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797685 | TGTCGTTTCTCTTGC[A/G]GGGCTGGTCGGGAAT | 57602 |
rs141889413 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78816455 | ACATGGTGGAACCCC[A/G]TCTCTACTAAAAATA | 57602 |
rs142036786 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78791415 | TGAGCCACCGTGCCC[A/G]GCCCTGGCCTTCTTT | 57602 |
rs142065427 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP36 | GRCh38.p7 | 17:78828800 | GCTTAAGGCCAGGAA[C/T]TTAAGACCAGCCTGG | 57602 |
rs142110941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838577 | ATACACAGAAGCCTC[A/G]CAGACTCACCTGGGA | 57602 |
rs142147823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78829322 | ATTTCACTAGTATTA[C/T]TTACTTATAAAAAGA | 57602 |
rs142149420 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797581 | GCAGCAGCCTCTGCC[A/G]GCACAGACCACTGTC | 57602 |
rs142162440 | snp | A/G | 8.24165e-05 | 0.00641883 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814485 | GCATAGAGTCCATAC[A/G]TGACAGGATCACCAT | 57602 |
rs142172537 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78831483 | CCGTGTGTGGTGGCA[A/G]TCACCTGTAATCCCA | 57602 |
rs142203151 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78827783 | GCATGATGGCATGTG[C/T]CTGTAGTCCCAGCTA | 57602 |
rs142216826 | snp | C/T | 0.0043778 | 0.0465804 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821050 | AGACGCTCTTGCACA[C/T]GGAGCACTTCACTGC | 57602 |
rs142237548 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78799305 | GGAACAAAGATGTCA[C/T]GTTTGGTCTCGAAGT | 57602 |
rs142254504 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78838092 | CATCGTGAGACCCCA[C/T]CTTTAAAACAAAAAA | 57602 |
rs142483821 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78828090 | CAGTCAAGTGTGGTG[C/T]GCCTGTAATCCCAGC | 57602 |
rs142518712 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78803001 | TGTAGTGCAGTGACG[A/C]GATCTCAGCTCACTG | 57602 |
rs142555796 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841132 | CACACCTGGCGGCGT[C/G]GCGGACGCCTGAAGT | 57602 |
rs142594430 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78811724 | AATAAAAAAATTAGC[C/T]ATGCATGGTGGCACA | 57602 |
rs142617524 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807389 | CTGGTCCCAGGCAGC[C/T]CCTGAGCAGTTCTGG | 57602 |
rs142620769 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78806611 | GCTCTGCGCTTCCTG[C/T]CCGCCCCACCCCTGC | 57602 |
rs142625598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78788689 | GCCAAGGACGAGATG[C/T]GGAGGGACTCGGGTC | 57602 |
rs142691788 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842243 | GCAGCGAGCTGAGAT[A/G]TCGCCACTGCACTCC | 57602 |
rs142705072 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78807760 | GCATGCTCAAGATAA[A/G]TTATTTATCTGGACT | 57602 |
rs142725072 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | USP36 | GRCh38.p7 | 17:78810003 | AGGCGCACGCCACCA[A/T]GCCCAGCTAACTTTT | 57602 |
rs142785001 | snp | A/T | 0.00159617 | 0.0282053 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835283 | ACCCACACTCACAGC[A/T]GCGAGCATGCTCCTT | 57602 |
rs142887697 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | USP36 | GRCh38.p7 | 17:78789109 | GGCTGAGGCAGAAGA[A/C]TCACTTGAACCTGGG | 57602 |
rs142888715 | in-del | -/AAAGACTTCTCACCAACTGA | 0.124491 | 0.216211 | intron-variant | USP36 | GRCh38.p7 | 17:78838496 | CTCATGAGAATTATC[-/AAAGACTTCTCACCAACTGA]ACAATCACTGCTGCG | 57602 |
rs143004059 | snp | C/T | 0.00241046 | 0.0346326 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835408 | CCCACGCGGAAGACC[C/T]GCTCCCACCTCAGAG | 57602 |
rs143010831 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78794001 | AGCCGCTTGCTTCCC[C/T]GGCTACTACTTGGCC | 57602 |
rs143011665 | snp | A/G | 0.00424341 | 0.0458661 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802330 | GGTGCATACCCATGC[A/G]GTCCCCAGGACACCA | 57602 |
rs143016615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821200 | TAGCCCCTGAAGCAT[A/C]CTGGTGTCCGAACAG | 57602 |
rs143059191 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78792384 | ACAGAGGGGGCACCT[C/T]GTCCAGCATCTCCAG | 57602 |
rs143061001 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78823933 | GGCCCAGTCTATGCA[A/C]AGTGCTTCAAGCACA | 57602 |
rs143094463 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78789869 | GCTCAGGGAAGGCAA[C/T]GTGAAGGGGAATTAG | 57602 |
rs143102313 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805298 | TTATAAGGCAAGAAA[C/T]GAAAAACACCCAAAC | 57602 |
rs143152002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794546 | GCCGGTGGGACTCTG[C/T]CCGCCGCCTGCGAGA | 57602 |
rs143161068 | snp | C/T | 3.33367e-05 | 0.00408255 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807246 | GGCCAGCGCTCTCGT[C/T]GTTCCCCTTCAGCCC | 57602 |
rs143164546 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | USP36 | GRCh38.p7 | 17:78826711 | GTGATGGCAACCATC[-/A]CATATAAGGGCTTAC | 57602 |
rs143211507 | snp | C/T | 0.000120682 | 0.00776702 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803829 | AGAGACACAAGGTCC[C/T]CGTTGACCTGAGGCA | 57602 |
rs143223744 | snp | A/G | 3.30814e-05 | 0.00406689 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807155 | GCCGCTCCACTCCTG[A/G]GGGTCTGGGGGGCCT | 57602 |
rs143240679 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78829605 | TCCTGTATTGTAGAG[A/G]AGGCAGCCATAGACA | 57602 |
rs143301368 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78821849 | GCACAGCGAAGAAAG[A/G]GCCCCAGCCTGCGTT | 57602 |
rs143307341 | snp | A/G/T | 0.000461631 | 0.0151858 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806238 | CGGAGGATGGTGAGG[A/G/T]GGGAGGTGGACGGAG | 57602 |
rs143366003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832723 | ACAGGCCTGGGATAG[C/T]AGAGTCTTACTGCCA | 57602 |
rs143395187 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78810491 | CAGGGTTTTGCCCAG[C/G]TTGGTCTCGAACTCC | 57602 |
rs143422402 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78838891 | CACGCGTGCACTCAG[G/T]ATGAGGCGGGTGGAC | 57602 |
rs143436236 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP36 | GRCh38.p7 | 17:78833126 | GCACTCCAGCCTGGG[C/T]GACAGAACGAGACTC | 57602 |
rs143475063 | snp | C/T | 0.00351973 | 0.0418028 | intron-variant | USP36 | GRCh38.p7 | 17:78806141 | GCACCCAGAAGATCC[C/T]GGCCCAAAGCTTACC | 57602 |
rs143571508 | snp | C/T | 0.00100471 | 0.0223907 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807531 | GCAGCTTTGGAGGAA[C/T]GCAGCCGTTCTGGGA | 57602 |
rs143597417 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797466 | CGTCAGCCCCGAGAA[A/G]CAAGGGATGGCTTGC | 57602 |
rs143600798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809204 | TAGTAAATTATGTAC[A/C]AAAATGTAAATCTTA | 57602 |
rs143626464 | snp | C/T | 3.29516e-05 | 0.00405891 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836181 | TTTGGGGTTGAGCAA[C/T]ACATATTTGCTCTTT | 57602 |
rs143666818 | snp | C/T | 0.000247184 | 0.0111144 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807085 | TGCTCCACTTGGCGG[C/T]GTTTTGGAGTGGCCA | 57602 |
rs143701541 | snp | G/T | 0.0527106 | 0.153555 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827343 | GCGGAAGTGTCGGGC[G/T]ATCTCTAAAAGAGGA | 57602 |
rs143765903 | snp | A/C/G | 0.000230697 | 0.0107377 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807086 | GCTCCACTTGGCGGC[A/C/G]TTTTGGAGTGGCCAG | 57602 |
rs143772552 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812919 | TCTTGGAGTGATCTG[A/G]AATCACACTCGGGCG | 57602 |
rs143816156 | snp | A/C/G | 0.000395602 | 0.0140589 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807097 | CGGCGTTTTGGAGTG[A/C/G]CCAGCGGTGGAACAG | 57602 |
rs143816809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824841 | CAGCAAGGGGCCGGC[A/G]GAAACCCTGCAAAAG | 57602 |
rs143856425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794877 | TCAGGCGTGGTGATG[C/T]GTGCCTGTACTCCCA | 57602 |
rs143942831 | snp | C/T | 1.64885e-05 | 0.00287123 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814462 | TGTAGCCCGAGTGCA[C/T]CAGGACAGCATAGAG | 57602 |
rs143963015 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | USP36 | GRCh38.p7 | 17:78828190 | CTGTCCTCCAGCCTA[C/G]GTATAAGAGCAAAAC | 57602 |
rs143995729 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP36 | GRCh38.p7 | 17:78822868 | CTGCAGGCCCTTTAC[C/T]AGGAGGCTGCGCAGT | 57602 |
rs144005453 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | USP36 | GRCh38.p7 | 17:78816308 | GGGACTATAGGCACG[C/T]GCCACCATGACTGGC | 57602 |
rs144058120 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796741 | GAAGGAGGTCTAAGT[C/T]CAACACCACGTTGTC | 57602 |
rs144079295 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78808477 | GCTAGCCTTGAATTC[C/T]TGAGCTCAAGCAATC | 57602 |
rs144099986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835941 | CAGATTTCCTTGCTA[C/T]CAACCCTGTATCATT | 57602 |
rs144214925 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP36 | GRCh38.p7 | 17:78794986 | GCACTCCAGCCTGGG[C/T]GACAGAGGGAGACTC | 57602 |
rs144324833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808707 | CCCTTCAGAGCACTT[A/C]TTACAACTGCATAGA | 57602 |
rs144379379 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78824598 | AAAACACACATCTTC[C/T]TAATATCCAAAGAAA | 57602 |
rs144381842 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807186 | TGGTGGAGTCGCTGC[C/T]GGCCGAGTGCTCTGG | 57602 |
rs144463621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78830834 | TTTCATTTTAGACTT[C/T]TGCTTGCCTTTTCTA | 57602 |
rs144466335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78810115 | CCTCCCAAAGTGCCC[A/G]GCCCCCCTCTTCTTT | 57602 |
rs144517101 | snp | A/G | 0.00168245 | 0.028955 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803452 | CTCCTTTCCTCCTCC[A/G]CTTCCTGCTGCTCGC | 57602 |
rs144554402 | snp | C/T | 0.00133495 | 0.025801 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806249 | GAGGGGGGAGGTGGA[C/T]GGAGGTCATTGCCGG | 57602 |
rs144571361 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP36 | GRCh38.p7 | 17:78833995 | TTCACACCTGTAATC[C/T]CAGCACTTTAGGAGG | 57602 |
rs144640900 | snp | C/T | 0.000148247 | 0.00860822 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818703 | GAAGTTGGCAAAGCG[C/T]TTGAGGGAAAGGGTT | 57602 |
rs144665968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78818171 | AAAAAGCCAGAGCAT[A/G]CAACGGCACCTGTTC | 57602 |
rs144734912 | snp | A/G | 8.23635e-05 | 0.00641677 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798996 | GCATCCTGACTGACC[A/G]CCGACATCTTGCCAT | 57602 |
rs144756950 | snp | C/T | 0.00233835 | 0.0341131 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802329 | CGGTGCATACCCATG[C/T]GGTCCCCAGGACACC | 57602 |
rs144862820 | snp | C/T | 8.62478e-05 | 0.00656631 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803832 | GACACAAGGTCCTCG[C/T]TGACCTGAGGCAGCG | 57602 |
rs144864410 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790721 | GGCCTTAAAAAAATC[A/T]CTGGTTTATGTAAAA | 57602 |
rs144889726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78823042 | AGACCATTCCACACC[C/T]GCAGGCTACACTTCC | 57602 |
rs144916519 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78814620 | TCAATTTGCCCTTTC[C/T]ATCCACAACCACACA | 57602 |
rs144952972 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78816824 | TGTTGAAATGCATAG[A/C]TCTTCAGTATATAGA | 57602 |
rs145087298 | snp | A/G | 0.000947351 | 0.0217435 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821024 | GTCCAAGTAGGGGTC[A/G]TAGGTGTCCGAGACG | 57602 |
rs145100246 | snp | C/T | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807053 | ACAGGGGACTTCAGC[C/T]TCACCGTCTTAGAAT | 57602 |
rs145213126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818967 | GGAAAGCTACCACAG[G/T]GAAATAAGACTACAG | 57602 |
rs145257561 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78829430 | AAATATTTTAGGGCT[C/G]ACAGCCCCTTAGTAG | 57602 |
rs145298376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817782 | AGAAACACATCTTCT[A/G]TGAAAATGCCACTAT | 57602 |
rs145346267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793757 | TTAAGGTCACTATTA[C/G]AGTTATGATGAGCCC | 57602 |
rs145375689 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78789495 | TAATTTTGCAGCATA[G/T]ACCTTGCAGAGAGGG | 57602 |
rs145417143 | in-del | -/TCTG | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78811348 | CTTTATCATCCTCTC[-/TCTG]TATGTATATGTACGT | 57602 |
rs145436112 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797274 | GCCTCTGCTCTCCAG[A/G]ACAGTTGAGAGCTAC | 57602 |
rs145444440 | snp | A/G | 0.000312956 | 0.0125052 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798479 | CAGACCAGAAGTTCC[A/G]TCGAGTCTGAAGTTT | 57602 |
rs145545790 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | USP36 | GRCh38.p7 | 17:78816047 | ATAGTGCCTGGCATG[C/G]CAGCTGTAGGCTGAG | 57602 |
rs145562419 | snp | A/C/T | 0.000199498 | 0.00998581 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802363 | CATTCGCGGATGGTG[A/C/T]GCAGCTGCTGGACTC | 57602 |
rs145591044 | snp | A/G | 0.00319455 | 0.039838 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803684 | CCCGTGGGGAGCCGC[A/G]GTGGCCTCCCTGATG | 57602 |
rs145619489 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | USP36 | GRCh38.p7 | 17:78832386 | AGGATCCAGTGGGGT[A/G]CAGGAAAAAAAGGCC | 57602 |
rs145638767 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78805053 | GACAGGATCTAGTGC[C/T]GAACCCAGTGAGGCT | 57602 |
rs145655217 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78840978 | TCCGTGTCGCCTACG[A/T]CACCTCCCCATCACG | 57602 |
rs145657048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78789493 | GCTAATTTTGCAGCA[C/T]AGACCTTGCAGAGAG | 57602 |
rs145684733 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78840894 | CGCTGCGCTAACTCC[G/T]AAAGGGTTGGGAGGC | 57602 |
rs145685427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806731 | AAACCTCCATGAGTC[A/G]CATGAGCATCACCAG | 57602 |
rs145731371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811367 | TATGTATATGTACGT[C/G]TGTATATATGTATGA | 57602 |
rs145768831 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | USP36 | GRCh38.p7 | 17:78804773 | ATTCAAGTATTTTTG[C/T]GAGCTCTAATGTAAA | 57602 |
rs145845613 | snp | G/T | 0.00874735 | 0.0655527 | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838664 | GGCTGAGTTTGGTTG[G/T]GCAGGTGCTACGCGG | 57602 |
rs145909229 | snp | A/C/T | 6.62563e-05 | 0.00575538 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835391 | GGTTGTGGAGTCCTG[A/C/T]GCCCACGCGGAAGAC | 57602 |
rs145977877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800156 | AAAAAAACCCTCCAA[A/G]ACCCCTTTAACCAGT | 57602 |
rs145987874 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836418 | AGATAACGAAATCCC[A/G]GGACAAAAACATCTC | 57602 |
rs146001432 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78788904 | ACAATGCTGGCTTCA[C/T]GAAAGAGAGATGAGG | 57602 |
rs146014293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839610 | AACCCAGTTTCACTC[A/G]AGATAAGTAACTTTG | 57602 |
rs146108910 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78798779 | ACACGCCCGGACAGG[C/T]CTGGGCAGCCTGGCT | 57602 |
rs146124160 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, missense | USP36 | GRCh38.p7 | 17:78823167 | GGGGACCAATACAGG[A/G]TCATTCAATTTTTAT | 57602 |
rs146137117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78802593 | GAAGGGGAGCAGGAG[C/T]GCACAGACACCCGCC | 57602 |
rs146168630 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813829 | CTTGACGTTGCTGGA[A/G]TGGACCAAGGAATCA | 57602 |
rs146186604 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821970 | CTCCAAAAATTTGAT[A/G]GACCAAGGTAGTAGC | 57602 |
rs146231280 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78810629 | GTGACCACCAACTTT[A/G]CAATTATATCATGTA | 57602 |
rs146291781 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | USP36 | GRCh38.p7 | 17:78802207 | GCGGTCCAACCCCTC[A/G]CCCAGTGCACGCCCA | 57602 |
rs146302851 | snp | A/G | 9.28617e-05 | 0.00681339 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807620 | TGCGGCTTCTTCATC[A/G]TCCCAGAGTCTTGTC | 57602 |
rs146351236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78824950 | AATGCTAAAAGCAAC[A/G]ATCCTCAATGAAGAC | 57602 |
rs146432997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793822 | GATTCCCCAGTGTCC[A/C]GACACCTGGGCTTTT | 57602 |
rs146557659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806754 | ATCACCAGATCAGGG[C/T]TCTCTCAACACCCCA | 57602 |
rs146583745 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78808753 | TGTATTTAGATGCTG[A/C]ATGTCAGCCTTCCCC | 57602 |
rs146676205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818206 | CATCAAAAGGACATG[A/G]ACAATGCAAGTCCCA | 57602 |
rs146702187 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78822600 | CATGTCCCCCGCACC[A/G]CTCACTAACTGGGAT | 57602 |
rs146706684 | snp | A/G | 9.999e-05 | 0.00707001 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807247 | GCCAGCGCTCTCGTC[A/G]TTCCCCTTCAGCCCA | 57602 |
rs146710968 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP36 | GRCh38.p7 | 17:78809710 | AATGATAGCTCAATG[C/T]AGCCTTGTGTTTAAG | 57602 |
rs146794733 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78832122 | AATCCATGACTACAC[A/G]GACATAGAGAGATTT | 57602 |
rs146823862 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78834108 | AAAAATTAGCCAGGC[A/G]TGGTGGCGTGCGTCT | 57602 |
rs146974392 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78823775 | TCAGGGTCCTGAAAA[A/G]AACTCAAAACTATCC | 57602 |
rs146984328 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78826091 | CCCAGTTCACTGAAG[A/G]GCAGACCTGGGATCA | 57602 |
rs147080650 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78835113 | GATTCACCTTCATGG[C/T]CCATTCTGCAGCAGG | 57602 |
rs147090135 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP36 | GRCh38.p7 | 17:78838246 | GGCATGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 57602 |
rs147090363 | snp | A/G | 0.00517822 | 0.0506191 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787133 | CGCACGCGCTACCAC[A/G]CCCTGCTAATTTTTG | 57602 |
rs147129971 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78833633 | CAAACCCTACAGGCC[A/G]GGCTCCTGAGCTGTG | 57602 |
rs147153153 | snp | A/G | 0.00167918 | 0.028927 | intron-variant | USP36 | GRCh38.p7 | 17:78806142 | CACCCAGAAGATCCC[A/G]GCCCAAAGCTTACCT | 57602 |
rs147163143 | snp | G/T | 0.000335591 | 0.0129492 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807581 | CCATTCCTGGATATG[G/T]GCACACCAATCTCTT | 57602 |
rs147255799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78816590 | GAGATGGTGCCACTG[C/T]ACTCTAGCCTGGGTG | 57602 |
rs147266244 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78820925 | CCTTTACTGTTCTGC[A/G]GGTTCTGTTTCACCC | 57602 |
rs147286136 | snp | A/G | 0.000155951 | 0.00882901 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802364 | ATTCGCGGATGGTGC[A/G]CAGCTGCTGGACTCG | 57602 |
rs147302564 | snp | C/T | 6.86271e-05 | 0.00585738 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803797 | GGGGCTCACTGGCCT[C/T]TGGCAACTGGTGTGG | 57602 |
rs147398039 | snp | A/G/T | 4.95171e-05 | 0.00497559 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828913 | TTTCAGGTCTCGGAT[A/G/T]AAGGAGACGGGCTTG | 57602 |
rs147436899 | in-del | -/GAG | 0.0209421 | 0.100162 | intron-variant | USP36 | GRCh38.p7 | 17:78801705 | AGCTACATAGAGGGA[-/GAG]GAGGATTCACTTTTG | 57602 |
rs147469304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792643 | CAATTCTGGTGCTCA[C/T]TTGAGTTTGAGACCA | 57602 |
rs147469549 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | USP36 | GRCh38.p7 | 17:78824188 | TGGAGGGTGGGCAAT[C/G]AGCAATGGGAAGATG | 57602 |
rs147479636 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78794851 | ATCTCTACTAAAAAT[A/G]CAAAAATTAGTCAGG | 57602 |
rs147551808 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP36 | GRCh38.p7 | 17:78803096 | GGTGCATGCCACCAT[A/G]CCCAACCAATTTTTG | 57602 |
rs147614171 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826467 | GCAGTTTTCTTTCTG[A/T]AAGTCTTATTTACGT | 57602 |
rs147624321 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78829176 | CTGCTGACTGGGTGA[C/G]CACCAAGGAAATGTT | 57602 |
rs147631589 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78824617 | TATCCAAAGAAATTT[C/G]AGAAATAAAGAAAAA | 57602 |
rs147635914 | snp | A/G | 0.0125733 | 0.0782851 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828991 | GACACACAGCATGCA[A/G]AAGCTTCCCTGGTGG | 57602 |
rs147654625 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78814156 | ATGGCCGATTTTGCC[A/G]GGGTTCTAAGGATGG | 57602 |
rs147716446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78838272 | CAGCTACGCAGGAGG[C/T]TGAGGCAGAGAATTG | 57602 |
rs147845110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806464 | ATGGTAGAAGAAGAA[A/C]CAGAAAAGTATTTTT | 57602 |
rs147865814 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP36 | GRCh38.p7 | 17:78789373 | CCCAGAAGGAGTAGG[C/T]TGAACAGTGGTTAGA | 57602 |
rs147867694 | snp | A/G | 0.00031294 | 0.0125049 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818724 | GGAAAGGGTTAAGAC[A/G]TTGGATGTTCTGTGG | 57602 |
rs147938729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78814690 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 57602 |
rs147962387 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78816912 | CCCACATCCCAGTCA[C/T]TGCCCCCATCTCAAA | 57602 |
rs147978428 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78810121 | AAAGTGCCCGGCCCC[A/C]CTCTTCTTTTTTTTG | 57602 |
rs147989943 | snp | A/G | 0.0020548 | 0.0319871 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827280 | GGCTTTCTGCATGGC[A/G]TCGATGGTGTACCGC | 57602 |
rs148007252 | snp | A/G | 4.94197e-05 | 0.00497066 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798929 | TCGGTCAAACTCTTC[A/G]TCCCAGTCATCAACC | 57602 |
rs148065333 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78819230 | CAGACCTAAAGAAGA[C/G]TAAAGCAGAATTAAG | 57602 |
rs148094776 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | USP36 | GRCh38.p7 | 17:78827404 | TCATCAAACGGCCTG[C/T]GGCTGCTTTCCTGAA | 57602 |
rs148192093 | snp | C/G | 0.00198003 | 0.0314022 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835366 | GCATTGAGAAAGCAG[C/G]TGTTGCCAAGGTTGT | 57602 |
rs148226667 | snp | C/T | 5.16391e-05 | 0.00508103 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835429 | CACCTCAGAGACAGT[C/T]GCTCCGTGGGGAAAA | 57602 |
rs148308500 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP36 | GRCh38.p7 | 17:78801495 | TCACTCAAGCTCGGC[C/T]CCCTATACCAAGCAG | 57602 |
rs148348436 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP36 | GRCh38.p7 | 17:78832938 | CAGATCACCTGAGGT[C/T]GAGAGTTCAAGACCA | 57602 |
rs148357920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78805726 | TCTTAACCTGCATGA[C/T]GCTAGCAGGCAAGAC | 57602 |
rs148422156 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78802812 | GATGAAACGGCAGAT[A/C]CTGGCCTGGCCCGGG | 57602 |
rs148452104 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP36 | GRCh38.p7 | 17:78834018 | TTAGGAGGCCAAGGC[A/G]GTTGGATCACCTGAG | 57602 |
rs148472270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806542 | CAACAATCACATCCA[C/T]GTGCCGTGGCTGCCC | 57602 |
rs148628582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828197 | CCAGCCTAGGTATAA[A/G]AGCAAAACCCTGTCT | 57602 |
rs148661480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788924 | GAGAGATGAGGCCAG[C/G]TGCGGTGACTCACGC | 57602 |
rs148713103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78838043 | TGAGCTATGATTACG[C/T]CTGTGAATAGCCAGT | 57602 |
rs148746275 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78791281 | CTGGGATTACAGGCA[C/T]GCACCACCATGCCCG | 57602 |
rs148941450 | snp | A/C | 0.000890701 | 0.0210845 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835282 | AACCCACACTCACAG[A/C]TGCGAGCATGCTCCT | 57602 |
rs148943735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805035 | TGAGCAAGGCGTGTC[C/T]GGGACAGGATCTAGT | 57602 |
rs148947886 | snp | A/G | 0.00373314 | 0.0430422 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812896 | AATAATCCCATTGCC[A/G]ATGTTCTTCTTGGAG | 57602 |
rs148975174 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78814709 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 57602 |
rs149071819 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78818070 | AGCCCAGGTGACAGA[C/G]TGAGACCCTGTCTTA | 57602 |
rs149099006 | snp | C/G/T | 9.88511e-05 | 0.00702975 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807063 | TCAGCTTCACCGTCT[C/G/T]AGAATCTGCTCCACT | 57602 |
rs149121986 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78823047 | ATTCCACACCCGCAG[A/G]CTACACTTCCCCTCC | 57602 |
rs149154662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78829594 | CACAACTATGCTCCT[A/G]TATTGTAGAGGAGGC | 57602 |
rs149178219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800755 | CCATGCGGCCCCCAG[C/T]GCCTCCTTGCTGAGC | 57602 |
rs149187688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78789759 | TGCCACGGTTTGGGC[A/G]TTCACTTCAAATAGA | 57602 |
rs149205576 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78832496 | GAAGGAAGACCAGGC[A/G]TTCCCCTTGAAGGGA | 57602 |
rs149235794 | in-del | -/C | 0.0681886 | 0.171594 | intron-variant | USP36 | GRCh38.p7 | 17:78793703 | TACCAAGACTTGAGG[-/C]CAGGGATTCTCACAG | 57602 |
rs149270390 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78830744 | ACATTAAAATGCTAT[C/T]ATTTACACAAAATTC | 57602 |
rs149302673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790981 | AACCAATGAAAACAC[A/G]CATGCAAGACATGTA | 57602 |
rs149344652 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799748 | CTCCATTCCAAGACA[C/T]AGGAGGGGCCTGGCT | 57602 |
rs149420360 | snp | C/G | 0.000296531 | 0.0121728 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807005 | GGTGGAGGAGACATG[C/G]TGCTTGCAGGCTCAG | 57602 |
rs149460713 | snp | C/T | 4.97921e-05 | 0.00498935 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835399 | AGTCCTGCGCCCACG[C/T]GGAAGACCCGCTCCC | 57602 |
rs149463432 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78812545 | ATACAAAAAAAATTA[G/T]CCGGGCGTGGTTCGG | 57602 |
rs149516702 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78816306 | CTGGGACTATAGGCA[C/T]GCGCCACCATGACTG | 57602 |
rs149597018 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78820846 | AAACAGGTAAAGACA[A/G]TGGTCTGTACTGCAA | 57602 |
rs149649666 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78824492 | GAGCCTGCCGTGAGC[A/G]GAGATTGCACCACTG | 57602 |
rs149658711 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78825785 | CCAGGCCCCCTGCTA[C/T]AGGCTCGCTGCACTC | 57602 |
rs149701651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78802712 | TCCACACGCAGCCAC[A/G]GAGACAGTAGAGGGA | 57602 |
rs149793535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832093 | GTAATTTAGGAAAAT[A/G]TAACTCAAAAGTCAA | 57602 |
rs149829984 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78793249 | TCTTGAGGTAGCCTT[C/G]GAAGTCACTTACCAA | 57602 |
rs149894958 | snp | C/T | 1.64944e-05 | 0.00287175 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814454 | ATGGCAGCTGTAGCC[C/T]GAGTGCACCAGGACA | 57602 |
rs149956146 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78808440 | TATTTTGTAGAGATG[A/G]GGATCTTGCTATGTT | 57602 |
rs149984186 | snp | G/T | 3.30879e-05 | 0.00406729 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836355 | CTTCAACTTATCCAC[G/T]ATTGGCATGGTGCAT | 57602 |
rs149988159 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78814067 | CAAAGTGTGCTCTGC[A/G]TCCCAGTTCCTTCCT | 57602 |
rs150038138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78817257 | CACACAGTGACAGAA[C/T]TGCCTGGTGACACAT | 57602 |
rs150088686 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78815483 | TAGTTCTCTCACCAC[C/G]TGGTTCCTAACGATC | 57602 |
rs150112017 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787576 | CTGTTCGTGTGCTGG[G/T]AACACACAGGTCAAT | 57602 |
rs150133518 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP36 | GRCh38.p7 | 17:78829412 | CACATGGTAAATAGG[C/T]TAAAATATTTTAGGG | 57602 |
rs150152331 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78820128 | CACAGAACTTAGACT[C/T]GCATAAAAATTTGCC | 57602 |
rs150183947 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78814951 | GAGACTGTCTCAAAA[-/C]CTGCCCCGCCACAAA | 57602 |
rs150184807 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78827720 | GCAGCCTGGGTAACA[C/T]AGGGAGACTTCATCT | 57602 |
rs150265420 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78834578 | CAGCCTCCCGAGCAG[C/T]TGGGATTACAGGTGC | 57602 |
rs150308159 | snp | C/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842087 | TGAGGTCAGGAGTTC[C/G]AGACCAGCATGGCCA | 57602 |
rs150319139 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78812461 | TTGGGAGGCCGAGGC[A/G]GGCAGATCCTGAGGT | 57602 |
rs150342066 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78804454 | GACAAAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 57602 |
rs150350738 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78794445 | ACCTCACCCCACGGT[C/G]CTTCAGGCAGAGCTC | 57602 |
rs150372851 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | USP36 | GRCh38.p7 | 17:78804501 | AAACAAAAACAAAAA[A/C]AAAAAAACAAAGTTA | 57602 |
rs150437022 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821001 | TGTACCCGGATCTCC[A/G]GCGCGACGTCCAAGT | 57602 |
rs150481067 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78809546 | CCCCTGCAGGTGTGC[C/T]TGACACAGGGACTCT | 57602 |
rs150547254 | snp | G/T | 0.0102422 | 0.0708251 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827336 | TCCCAAAGCGGAAGT[G/T]TCGGGCGATCTCTAA | 57602 |
rs150571260 | in-del | -/GGGGGGGG | | | intron-variant | USP36 | GRCh38.p7 | 17:78805408 | AGTAAGGCAGAGGCT[-/GGGGGGGG]GTGGGCGACGCACAG | 57602 |
rs150583152 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78810390 | TCTCCCTGGCTCAAG[G/T]GATCCTCCCACCTCA | 57602 |
rs150599271 | snp | A/G | 6.59109e-05 | 0.0057403 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836238 | CTTGCTGGCTGGCTC[A/G]AACTCGATTTTCTGT | 57602 |
rs150616678 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78798043 | ACACATGCCAGATAT[A/T]CACACAACCCACATC | 57602 |
rs150634688 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78789150 | TGCAGTGAGTCGAGA[C/T]TGCGCCATTGCACCC | 57602 |
rs150645043 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | USP36 | GRCh38.p7 | 17:78840182 | GGGGGCGCGCGGAGT[C/T]TCCCCTCTCGTGTGT | 57602 |
rs150656248 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP36 | GRCh38.p7 | 17:78830661 | CCAAATCATTTCCCC[A/G]CAATATCTCCAACTC | 57602 |
rs150677846 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78821772 | AACTGCTCCAGTGGC[C/G]AGGCGGGCCAAGAGT | 57602 |
rs150785930 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78829903 | TGCCACCATGCCAGG[-/G]CTAATTTTTTGTATT | 57602 |
rs150802920 | snp | C/T | 0.00804073 | 0.0628959 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835488 | ACCACAGCTCTCATA[C/T]GTGTGCTCACTGCCT | 57602 |
rs150813194 | snp | A/C | 0.000153932 | 0.00877167 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803744 | CCTCTGCGGCTCTCC[A/C]ACAAAGGTCTTTTTC | 57602 |
rs150845794 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78813460 | GGCAGCTTCCCCACA[C/T]GGGAAGGGGCATTGG | 57602 |
rs150865699 | snp | A/G | 6.6154e-05 | 0.00575088 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807156 | CCGCTCCACTCCTGG[A/G]GGTCTGGGGGGCCTT | 57602 |
rs150924360 | snp | C/G | 0.00209072 | 0.0322644 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806198 | GCAACGACGGGGTGA[C/G]AGGTTTTCATGGGGT | 57602 |
rs150939686 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78825222 | GAAACATTCACAAAC[A/G]CTGGTCACCTATAAT | 57602 |
rs150961543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78815099 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTAGATCA | 57602 |
rs150970909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806661 | GGCCCACCCTCCCTC[A/G]GGTTCAGTCAGGATC | 57602 |
rs150976064 | snp | A/C/G | 0.000231025 | 0.0107453 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807406 | CTGAGCAGTTCTGGG[A/C/G]GAAAAGTGCTGTGGA | 57602 |
rs151054144 | in-del | -/C | 0.0197687 | 0.0974348 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78840996 | CTCCCCATCACGGGA[-/C]CCCCGCCAGCCTACG | 57602 |
rs151065333 | snp | A/G | 0.000978523 | 0.0220976 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835286 | CACACTCACAGCTGC[A/G]AGCATGCTCCTTGGA | 57602 |
rs151110666 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78793027 | GCCCCCCTCACCCCC[A/C/G]CAGGAAGGCTTTAAA | 57602 |
rs151123050 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78811695 | TAATAAAGTGAAACC[C/T]CGTCTCCACTAAAAA | 57602 |
rs151130507 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78828807 | GCCAGGAATTTAAGA[A/C/T]CAGCCTGGGCAACAT | 57602 |
rs151175239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790018 | TCAACAAATATTTAC[C/T]GGGTGGCTGGTAAGT | 57602 |
rs151183976 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78831575 | CCGAGACTGTGGCAA[C/G]TGCACTCCAGCATAA | 57602 |
rs151236243 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78809497 | TATTTGGAAAATCAC[A/G]TTTGTAATGAAAATG | 57602 |
rs151312884 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796174 | CTGATTTGGAGGAGA[A/G]AAGGGAGAGAAAGGA | 57602 |
rs151321204 | snp | C/T | 0.000962287 | 0.0219139 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802405 | CATCTTGGGGCTTGG[C/T]ACTCCTTGGGCATTT | 57602 |
rs151331497 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78838152 | CTTGGGAGGCCGAGA[C/T]GGGTGGATCAGGAGG | 57602 |
rs180840934 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796661 | CTGCCCCAGGGAGAG[C/G]GGGTGCAGACAGCGA | 57602 |
rs180854132 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78815652 | AGACTTTTAATCAAC[C/T]GGATCAGAAGAAAGG | 57602 |
rs180869133 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833134 | GCCTGGGCGACAGAA[C/G/T]GAGACTCCATCTCCA | 57602 |
rs181127788 | snp | A/G | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78807849 | ACAGGGACCACAGCC[A/G]TGTACCACCACACCT | 57602 |
rs181144208 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78823925 | TGAAAGCAGGCCCAG[G/T]CTATGCAAAGTGCTT | 57602 |
rs181203001 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787255 | TGCTGGGATTACAGG[C/T]GTGAGTCACCATGCC | 57602 |
rs181228103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815066 | TGGCCAGGTGCGGTG[A/G]CTCACGCCTGTAATC | 57602 |
rs181237565 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795783 | GCCATGCAACCAGGA[C/T]GCGGGGCAGGCAAGT | 57602 |
rs181246074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832844 | AATAGGGGCTACAAT[A/T]AGCCATCTCAACAAT | 57602 |
rs181453846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78791797 | CTGGTTTCTTGCCTT[A/G]AAAGATTGTCCTGGA | 57602 |
rs181589906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811851 | CCAGCCTGGGCGACA[C/G]AATGAGACTCCGTCT | 57602 |
rs181600246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811365 | TGTATGTATATGTAC[A/G]TGTGTATATATGTAT | 57602 |
rs181612209 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78828598 | AGTCTGCACCACCAC[A/G]TGCAGGGCTGTTAGC | 57602 |
rs181672539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78791463 | TCAAACCTGACTCCA[A/G]CCTGACCCTACTTTA | 57602 |
rs181734276 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78802951 | ATTTTTTCTTTTTTC[G/T]TTTTTTTTAGACAGG | 57602 |
rs181755563 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838726 | GCCTGTTCAAACACC[A/G]AAGCCGCAGAGCGGG | 57602 |
rs181763430 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78792278 | TCCTAAGGGAAGAGT[A/G]AGACACGGGAGCAGA | 57602 |
rs181773477 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78838317 | GCAGAGGTTGGAGTG[A/C]GCCGAGATCGCGCCA | 57602 |
rs181775206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78812279 | CGACACCTGTAAGTG[A/G]TGCTGGTCTCATGAG | 57602 |
rs181779751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78829315 | TTTTCAGATTTCACT[A/G]GTATTATTTACTTAT | 57602 |
rs181961932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78819601 | GCTCGTGCTCTGCCA[C/T]GTCCTCTTGGTGTGG | 57602 |
rs181966734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820122 | GCAAATCACAGAACT[C/T]AGACTCGCATAAAAA | 57602 |
rs181971219 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833780 | GGTAGTATTTTCCTA[A/C/T]AATTTTTATATCTAT | 57602 |
rs182262524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818014 | CGCTTGAGCTTGGGA[A/G]GTCAAGACTGTAGTG | 57602 |
rs182326062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823369 | CCCTCTGTCATCCAG[A/C]AGCCCGCAAGCACCA | 57602 |
rs182332449 | snp | C/T | 0.00072098 | 0.0189729 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802327 | CCCGGTGCATACCCA[C/T]GCGGTCCCCAGGACA | 57602 |
rs182334331 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797645 | TGTCCAGCAGGTGTG[C/T]GGCCACCTCTGCTCA | 57602 |
rs182335364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799183 | GGAGGACGGCTCGAC[G/T]CCCATGTGTGGTCGG | 57602 |
rs182369506 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78825957 | TGCAAACGCTGCTGG[A/G]GTCCACTGTCTTCAC | 57602 |
rs182433189 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78809631 | AAGTGGGGCTTCCTT[C/T]GTTTTTCTGGGGTTT | 57602 |
rs182600144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816191 | AAGAAACACAGTCTC[A/G]CTCTGTCACCCAGGC | 57602 |
rs182609053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808401 | GACTATAGGAGTAGA[A/C]CACCACACCCGAATA | 57602 |
rs182774019 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78803062 | TCCCACCTCAGCCTC[A/C]TGAGTAGCTGGGACT | 57602 |
rs182774122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820338 | AAAAATTAGCCAGGC[A/G]TGGTGGTGCATGCCT | 57602 |
rs182788339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839259 | CACAGATGGAGAACC[G/T]CACAGGGAGCACATG | 57602 |
rs182847424 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78804919 | CCCGGGCAGGAAATG[A/G]GCCTCATAAGGAAAG | 57602 |
rs182847520 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP36 | GRCh38.p7 | 17:78790106 | CCTTTTTTTTTTTTT[C/T]GAGACGAAGTCTCGC | 57602 |
rs182847541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817419 | GGTGTCATTCCAAAC[C/G]ACATAACCAGGCTCT | 57602 |
rs182865910 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP36 | GRCh38.p7 | 17:78821222 | TCCGAACAGAGAGCT[C/T]TCTTTCACCACTGAA | 57602 |
rs182869864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788809 | CACTGCCTGATGTCA[C/T]TCCCCTCCACCAAGG | 57602 |
rs182925919 | snp | A/C | 0.0006094 | 0.017445 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812960 | GAGGAGGAGCCTGTC[A/C]TGGAGATGAGGCCCT | 57602 |
rs183125701 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78793003 | TTACAGGTGTGAGCC[A/G/T]CCGCGCCCGCCCCCC | 57602 |
rs183133682 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78798150 | CCCAACACACACTAC[A/G]CACACCCCCTTATAC | 57602 |
rs183138400 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78831017 | GGATCGCGAGGTCAG[A/G]AGGTTGAGACCATCC | 57602 |
rs183156381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835071 | ATTATTTACAGAAAA[A/G]CTTGGCGAACACAGC | 57602 |
rs183386108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78789054 | ATATGAAAATTAGCC[A/G]GGCGTGATGGCATGC | 57602 |
rs183389993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809099 | CTGCACATGCACTAA[A/G]GTGATCTTCATTTGA | 57602 |
rs183392115 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825699 | AGACTCTGGTTAATT[G/T]GACTGACTGAAGCCC | 57602 |
rs183410457 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841518 | CACCCACTCCCTCCA[A/C]AAGCTTTGTCCTCTG | 57602 |
rs183544527 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837597 | AAGAGACCCCTGCAC[C/T]TCTCCAATCGCTACC | 57602 |
rs183617780 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78801951 | CCAAGGGAGCAGACT[C/T]GGGGGTGGGGGGTGA | 57602 |
rs183619655 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78819491 | AAGTAAAAAATGAAA[C/G]CCAAAGAAAACACTC | 57602 |
rs183705928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792478 | CCAACCACCCAGCCC[C/G]TCTGGGAGGCATCAG | 57602 |
rs183744355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78820647 | ACAAAGCCAAGGCTG[C/T]TCTCCCAGGTGAGGC | 57602 |
rs183805620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78801121 | AGCTGGGACTAGAGG[C/T]GCCCGCCACCATGCC | 57602 |
rs183941112 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78804262 | AGGTCAGAAGTTTGA[A/G]ACCAGCCTAGCCAAC | 57602 |
rs183948807 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78840745 | GCCTACCCCGGCCTC[C/T]CCGCGGGCGCGCCAC | 57602 |
rs184006699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828666 | TTCTCTCCCTTCTAC[C/G]AACTCCCCAGCACCT | 57602 |
rs184045860 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842232 | AGGCGGAGGTTGCAG[C/T]GAGCTGAGATGTCGC | 57602 |
rs184048871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835578 | ACAAAAAGAAACTCC[C/T]GAAGCATACACTTAG | 57602 |
rs184119073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821718 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC | 57602 |
rs184120608 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78805415 | GCAGAGGCTGTGGGC[A/G]ACGCACAGTCATACC | 57602 |
rs184189100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818392 | TTCCTGGGCCCTGTC[C/T]TCCAGAGATTCAAAT | 57602 |
rs184319400 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | USP36 | GRCh38.p7 | 17:78810257 | CTTACTGAATATTCT[C/T]TGTGCTGATGGGATC | 57602 |
rs184443218 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78790841 | CTACCTAAATACCTA[A/C/G]ATCCTGCTTAAGGGA | 57602 |
rs184457404 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78826573 | CATTCTAGGTATATT[C/T]CCTAAACTATTTAAA | 57602 |
rs184562882 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78818859 | ACGCTAAGTTAATAA[A/C]AGCAACAACTGCTCT | 57602 |
rs184567725 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78791530 | CCTTGAGAAAGCAAC[C/T]TGAAGCAACAGTTTG | 57602 |
rs184711974 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836998 | GTGTAAAATGCACAC[C/T]AGATTTTGAAGAGAA | 57602 |
rs184718750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78811437 | CCATTTGAGTAAATT[A/G]CAGACATGATGTTCT | 57602 |
rs184724468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814760 | TCGAGATCAGCCTGA[C/T]CAATATAGCGAAACC | 57602 |
rs184738262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78831516 | TACTTGGGAGGATGA[A/G]GGAAGAGAATCGCTT | 57602 |
rs184796856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793919 | CCTGTACTGGTAAGA[A/T]GCCAACACGTCCACT | 57602 |
rs184827335 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796006 | TCCCTTCCCTATCTG[G/T]TTGATGACTTCGGTG | 57602 |
rs184949094 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78815321 | TCGCAACAGAGCGAG[A/T]CTCCATCTCAAAACA | 57602 |
rs184965426 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78810775 | GACTGCCTGTGTGTG[A/G]GGTTCAACTCTTCAT | 57602 |
rs184970831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828518 | AGCTACCTGTCCTGA[C/T]CTGCCCCCACTAAGA | 57602 |
rs185050395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78791408 | ACAGGCATGAGCCAC[A/C]GTGCCCGGCCCTGGC | 57602 |
rs185151472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814936 | GCCTGGGCGACAGAG[C/T]GAGACTGTCTCAAAA | 57602 |
rs185218980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833413 | CAGCCTCCCAAGTAG[C/G]TGGGATTACAGGTGT | 57602 |
rs185247824 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78820388 | AGGATCACTTAAGCC[G/T]AGAGGTCAACACTAC | 57602 |
rs185249320 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78803227 | CAGGTGTGAGCCACC[A/G]CACCCAGCCAGAGGA | 57602 |
rs185263667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839815 | AATCCCTCCGACGCA[A/C]ACACCATCCACACTC | 57602 |
rs185266773 | snp | A/G | 0.0103295 | 0.0711199 | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795241 | GAGCTGCCTCACCTC[A/G]CTTGTTCTTACTTGG | 57602 |
rs185283962 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78832368 | CCCACTTAGGGGTCA[C/T]TCAGGATCCAGTGGG | 57602 |
rs185392724 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78822535 | CACCCGTCTCAGAGA[C/G]GACAGCGGAGTCAGA | 57602 |
rs185512219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78806071 | TCCTGTGAGGTTGGC[A/G]ATTCGTCCAACTCCT | 57602 |
rs185529417 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842363 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCG | 57602 |