SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs535664839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466770 | AAAAAATTAGAATCC[A/G]CATATTTGGTGTATA | 10054 |
rs535720884 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453399 | ACAGGAAAAACTTGG[A/C]TTGTATTGCCTTATT | 10054 |
rs535740244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432141 | AGTTTAATACTTTTA[A/G]TAAATAAGTTACTTG | 10054 |
rs535881270 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442934 | GTTGTACAAAGGATT[A/T]CTGTAAGATAACTTT | 10054 |
rs535905628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34468271 | TGAGAATTTTGGAGA[C/T]GAACATTCAGATTAT | 10054 |
rs535930010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460319 | TGAATCCCCACGGCT[C/T]TCCTGCTTGCTCTAA | 10054 |
rs535992005 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426926 | CTCTATTTTTTAAAT[A/C]TACATCAAAAGCTTT | 10054 |
rs536048012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426254 | TTGGGTGCTGGTGCC[A/G]GGGCCGGGGCCGGGC | 10054 |
rs536050169 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34432927 | ACCTCCTTACCCTGT[A/G]TTGCTTTCCCAGTGC | 10054 |
rs536113477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34439163 | GAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 10054 |
rs536243977 | snp | G/T | 0.000296703 | 0.0121763 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428504 | GGTGCTGGTGGTGGG[G/T]GCGGGCGGCATCGGC | 10054 |
rs536255457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435338 | GAGAGGCAGAGGTTG[C/T]AGTAAGCTGAGATTG | 10054 |
rs536294164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34461236 | TTTCGAAGGTTTCTA[A/G]GCCCTGTGTTTCCCT | 10054 |
rs536432448 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34456653 | ACCTCCACCTCCCAA[A/G]TAGAAGTGATTCTCC | 10054 |
rs536447611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440824 | CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 10054 |
rs536452692 | snp | A/C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34452768 | TGTTGAAGATTAGTC[A/C/G]TGGGTCTTAAGGCAT | 10054 |
rs536459951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440047 | ACTTACTAAGTGCCC[A/T]GTGCGGTGGCTCAGG | 10054 |
rs536522930 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBA2 | GRCh38.p7 | 19:34446690 | TCTCAGCTTGCTGCA[A/G]CCTCTGCCTCCTGGT | 10054 |
rs536680033 | snp | C/T | 0.000184637 | 0.00960647 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469091 | ATGAAGAAGATTCTT[C/T]AAATAATGCCGACGT | 10054 |
rs536717986 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34434511 | TCTGCCTTCATTTCT[A/G]TCATGTATTATCTGC | 10054 |
rs536738393 | snp | C/T | 4.97442e-05 | 0.00498695 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467022 | CTCCACAGGTGAGTA[C/T]GGCCCCAGCCAGCAG | 10054 |
rs536818715 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34428076 | TGGGGGTGACACTTG[G/T]TAATTTGTAAGAGCT | 10054 |
rs536823411 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34431770 | ATAAATAAGGTACTA[C/T]GTAAGTAGATAACAG | 10054 |
rs536894456 | snp | A/G | 0.000386701 | 0.0138997 | intron-variant | UBA2 | GRCh38.p7 | 19:34463983 | CAACCTGACTGCTCT[A/G]TGAAGATGTAACTGA | 10054 |
rs536906161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463385 | AACAAATACCACAAC[C/G]CAGGTGGCTTAAACA | 10054 |
rs536968848 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469775 | CCTGGTATGTCTGTG[C/T]AAGAAGCCAATTTTT | 10054 |
rs537038333 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427336 | CCTTGATAAGTGTTA[C/G]TTATTTTTTCTTTCT | 10054 |
rs537041879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34434426 | TGGCGTGAAATTACT[C/T]TCTTAACCTGACTCA | 10054 |
rs537048553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34433828 | GCCGGTGTGGTGGCA[C/T]GTGCCTGTAGTCCCA | 10054 |
rs537052237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440779 | TAAAAATACAAAATT[A/G]GCCGGACATGGTGGT | 10054 |
rs537067697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426181 | AAATATGTTTGTATG[C/T]ACCTTATTTTAACTC | 10054 |
rs537118474 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34456428 | CTCGATGCACTCTTA[A/T]AATATTTTATTTTCA | 10054 |
rs537222141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446639 | TTTTGAGAGAGAATC[C/T]TGCTCTGTCGCCCAG | 10054 |
rs537255015 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453867 | CGTCTTTTGGCCTGG[A/T]TTCTGTGTTTGTCCA | 10054 |
rs537273761 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469709 | GTTAGATGGCACTAT[A/G]TATATTAATGTAAAA | 10054 |
rs537281416 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34456393 | TACTGGGATTTCAGG[C/T]GTGAGCTATTGCGCC | 10054 |
rs537286720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34454014 | AGTTCCTAGAAGCTG[A/G]TGATTCTTGGTGTTC | 10054 |
rs537297068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453471 | AGTTTGGCAAAGGGG[A/T]GTGAAAAAGAGTCAT | 10054 |
rs537374497 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427861 | CTTACCATTTTGCAT[G/T]GTTTACATTTTTTTC | 10054 |
rs537486441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34448086 | CAGTGGGAATCCATT[A/G]AAAGGTGGTCTTACA | 10054 |
rs537559139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463194 | AGACTGCTCAAGTCT[C/G]GGATGCACTCTGGCC | 10054 |
rs537560876 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34455265 | GGGAAGATACTCCTC[A/C]CCCTCCACTAAGCAC | 10054 |
rs537646387 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | UBA2 | GRCh38.p7 | 19:34436132 | TCAAAAAAAAAAAAA[A/C]CAAAAAATTCTGTTG | 10054 |
rs537679673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462547 | CTGGAAAAGAACTAG[A/G]AGAAACTGTTAGTAT | 10054 |
rs538171051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457543 | AACAAATCTTTCTCC[C/G]TCTGTAGCCTGCTTG | 10054 |
rs538304055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462271 | CAGGTGATAGATTTG[A/C]GATTTGCAAAGTCAG | 10054 |
rs538316241 | snp | C/T | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470212 | TGCAGTGAGCCAAGA[C/T]TGTGCTATTGCTACT | 10054 |
rs538369337 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34429891 | ATTTTGTACTTGAAA[G/T]AGTAATTCGATTGAA | 10054 |
rs538466627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34441539 | CTCAACCCGATAAAG[A/G]GTATTTTGTAGAAAC | 10054 |
rs538478814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450567 | TGTTCTGGTGGTCCG[C/T]CCTATGTACACAGAT | 10054 |
rs538493245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34449863 | CTTGGAGGCATTGCT[C/G]ACTGGCATCCCTAGG | 10054 |
rs538526220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447917 | GTATGTACAAGGAAA[C/T]TCTGAATAGGGTACA | 10054 |
rs538666484 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437384 | GGAGGCCAAGGCGGG[C/T]GGATCACCTGAGGTA | 10054 |
rs538835717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435405 | TCTGTCTCAAAAAAC[A/G]AACTTAAAATGCTAT | 10054 |
rs538930473 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461308 | TATTCATACTTTGTG[A/C]GGTCCTGATGGCGAT | 10054 |
rs539044099 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34437253 | AGGTATGAGCCACCA[C/T]GCCCGGCCAGACATT | 10054 |
rs539046067 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430236 | TTAATATATTTTCAG[A/T]TAGTGTTTACCTCGA | 10054 |
rs539056591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436704 | TACATTTGAAGAGTC[A/G]TTTTCCATGTTTTGA | 10054 |
rs539116088 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34469937 | CCTTATATCTACTGC[A/G]GGAATGTCAAATTCT | 10054 |
rs539172277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436052 | TTGAACCGGGGAAGC[A/G]GAGGTTGCGGTGAGC | 10054 |
rs539202607 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34463676 | GTGGTACAGTCACAC[A/C/G]CCTCACTGTGTAACT | 10054 |
rs539262260 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435321 | GCGAATCACTTGAAC[C/T]TGAGAGGCAGAGGTT | 10054 |
rs539385048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430762 | AAAAATGGGTGAAGC[A/T]CTCATTTCAGCTGAG | 10054 |
rs539427397 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453644 | TCCCGCCACCTCAGG[C/T]TCCCGAGTACCTGGG | 10054 |
rs539427775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34452270 | AAATATATTGATTTG[C/G]CTTGGATATTTTCAG | 10054 |
rs539429570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34444180 | CTCCTGCCTCAGGCT[C/T]CTGAGTAGCTGGGAT | 10054 |
rs539503627 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34458656 | ATTTTGCCATCTGGA[C/T]GGGAATTTTTAAGTC | 10054 |
rs539560660 | in-del | -/TTTG | 0.0166325 | 0.0896639 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427534 | GTTTCGGTGTTTTTT[-/TTTG]TTTGTTTGTTTGTTT | 10054 |
rs539561745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34458288 | AGGCCGGGCGCGGTG[A/G]CTCACGCCTGTAATC | 10054 |
rs539709033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437959 | CTTTGGGAGCCTGAG[G/T]CAGGAGAATTGCTTG | 10054 |
rs539805343 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34456964 | GAACTTATTAAAATG[C/T]CTGTTATTTCCCATC | 10054 |
rs539854853 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34435617 | GGCAGATGACTTGAG[G/T]TCAGGAGTTCGAGAC | 10054 |
rs539887958 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449482 | GTATTGATGGATTAA[G/T]TATATTTTGATAGAA | 10054 |
rs539910816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441749 | AACATGGCGAAACCC[C/T]GTCTCTACTAAAAAT | 10054 |
rs540025944 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34438496 | TTAGTTTATCATAAA[A/G]TAAGCATTTTGGAGT | 10054 |
rs540028235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432010 | AAAGTCATTCAGCTT[C/T]TTTAAAAAAAATGAT | 10054 |
rs540070762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464387 | ACACGGTGAAACCCC[A/G]TCTCTGCTAAAAATG | 10054 |
rs540143955 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470030 | AAGGCTGAGGCAGGT[A/G]GATCACCTGAGGTCA | 10054 |
rs540234811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34438998 | CGGATCACCTGAGCG[C/T]AGGAGTTTGAGACCA | 10054 |
rs540293527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435134 | CAGGTGCAGTGGCTC[A/G]TACCTGTAATCCCAG | 10054 |
rs540562180 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBA2 | GRCh38.p7 | 19:34439857 | GAATGAGAAGGAAGG[A/G]TATTAATTGAAGTAA | 10054 |
rs540579435 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465115 | CCCCCTATTCTGATA[C/T]ATTCATGTGTTGACC | 10054 |
rs540611275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34468133 | AATATTTACTCCTCT[C/T]CCTTTCTTCCTTTAG | 10054 |
rs540618992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443131 | TAATCTTGTTCATTG[C/T]TGAATTTCTATCCCC | 10054 |
rs540666583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450084 | GCTGTTTTCAATGTA[C/G]AGATTCTGTTAGAAC | 10054 |
rs540811943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34438101 | AAGAGTATTTGGTTT[A/G]GTAACACCTAAGATT | 10054 |
rs540816862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430863 | GAAATAATCCCGTGA[C/T]GGTGTAACTTTCATG | 10054 |
rs540902313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34436889 | TTGTGTATGTCAGTG[C/T]GTATTAAGTTGTTGA | 10054 |
rs541004123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436350 | TGTTGCCCAGGCTGC[A/C]GTGCAGTGGCGCGAT | 10054 |
rs541038718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432454 | AATTGTCCTTTATCT[A/G]TGGTGGTTTAGCTTG | 10054 |
rs541059607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458363 | GATCGAGACCATCCT[C/G]GCTAACACGGTGAAA | 10054 |
rs541100027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438880 | TAAATATGGTGAAGG[A/G]ATGCTTTAGTAGCTT | 10054 |
rs541133175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465411 | TGGGAGGCTGAGGCG[A/G]GTGGATCACGAGGTC | 10054 |
rs541201723 | in-del | -/TAG | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426403 | TTCTGGTGGGCATTC[-/TAG]GGGGGAGGAGAGCAG | 10054 |
rs541224403 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461879 | TTGTGAAACGGAGGG[A/G]GAGTAATAGGAGAGG | 10054 |
rs541266748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444348 | GCGTAAGCAACCGTG[C/T]CTATCCAAAACAATG | 10054 |
rs541290222 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34453974 | ATACAACTGAGTCTC[C/T]GGTGCCTTTGTTTAG | 10054 |
rs541293438 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34452935 | GGTTTTGTGATATTT[A/G]AAGGGTAACTTTTCA | 10054 |
rs541319127 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34459859 | AGCTTATGTTTTGGT[C/G/T]AAGGAAGTGGCAGGT | 10054 |
rs541356727 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458849 | CAACCCCAATTGTTA[C/T]GTATGTGCCAGCAAG | 10054 |
rs541395498 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426387 | GTTGTCTGCACAGCC[A/G]TTCTGGTGGGCATTC | 10054 |
rs541669819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450857 | CGATTCTCCCGCCTC[A/G]GCCTCCCGAGTAGCT | 10054 |
rs541681554 | snp | C/G | 3.62043e-05 | 0.00425451 | intron-variant | UBA2 | GRCh38.p7 | 19:34450382 | AAAGAATACATTTTA[C/G]TCTTGGAACACCTAA | 10054 |
rs541781029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457877 | TTTGTATATTTGCCT[C/T]GGTTCTTAATTATTT | 10054 |
rs541811251 | snp | A/G | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470152 | TAATTCCAGCTACTC[A/G]GGAGGCTAAGGCAGC | 10054 |
rs541873729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444249 | ATTTAGTAGAGACAG[A/G]GTTTCACCATGTTAG | 10054 |
rs541874310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430281 | TTAATGAATTCACAT[A/G]TTTTTATGGCATCCA | 10054 |
rs541930236 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34437581 | CGCCATTGCACTCCA[A/C]CCTGGGCAACGAGCG | 10054 |
rs541983921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34454027 | TGGTGATTCTTGGTG[G/T]TCTTGTCAGACTCAT | 10054 |
rs542053673 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467146 | TTGGTATTGATTGTT[A/G]TAATGGAGCTTTGAA | 10054 |
rs542070053 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34458346 | GGATCACGAGGTCAG[A/G]AGATCGAGACCATCC | 10054 |
rs542093685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459075 | TCTGGATTCCTGCAG[C/G]CTTTTCTGTCTGTGG | 10054 |
rs542131786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34465710 | TTCACAGTTAGATAA[C/T]GGAGTCAAAGTGGTC | 10054 |
rs542249283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438046 | ACAGAGCAAGACTCC[C/G]TCTCCCCACCGCCAA | 10054 |
rs542377493 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432568 | GGATTGTGTTTTTTT[G/T]GTGTGTGAGATAGGG | 10054 |
rs542378822 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444344 | ACAGGCGTAAGCAAC[C/T]GTGCCTATCCAAAAC | 10054 |
rs542412000 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBA2 | GRCh38.p7 | 19:34438243 | AAAAAAAAACACATA[C/T]AAGAAAATGGCTGCG | 10054 |
rs542464493 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460026 | TTCTTTTTTAGGAGC[G/T]GGTAGGATTTAACAG | 10054 |
rs542548884 | snp | C/T | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467756 | ACAGAGCGAGGCTTC[C/T]GGCTCCAAACAAACA | 10054 |
rs542624273 | in-del | -/TAT | 0.00478085 | 0.0486577 | intron-variant | UBA2 | GRCh38.p7 | 19:34468227 | TGGCATTCTTTGGAA[-/TAT]GTTTACTCTTGGCTC | 10054 |
rs542637379 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465282 | GTATACAAACATGCA[C/T]AGTGTTGGTGTGGTT | 10054 |
rs542668816 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34452691 | TTACTTAATTTTAAT[G/T]GTAATCAGTATTTTC | 10054 |
rs542694016 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34445557 | GATTCTCCTGCCTCA[A/G]CCTTCCGAGTAGCTG | 10054 |
rs542729887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459706 | CACTTCCTATTGTTC[C/T]CTGGTTGTGACCATC | 10054 |
rs542778905 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBA2 | GRCh38.p7 | 19:34443397 | AAGCTGTCCAAGCAC[A/G]TTGTGTTAAACTTTT | 10054 |
rs542787633 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427415 | CGCTGTATTGCTCAG[G/T]CTGGAGTGCAGTGGT | 10054 |
rs542794869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441128 | AAATTTAGCAAATGG[C/T]CTTTCATGATGAAAG | 10054 |
rs542801426 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426626 | TCCCATCTTCTGCTC[C/T]TGCAGTATCCCAGGA | 10054 |
rs542912624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34455418 | CTTAAGGCTAACACT[A/G]CTTGGATGTTCTCTT | 10054 |
rs542973874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462609 | TAAGCGTTTTCCTTA[C/T]AAATAATGAAAAAAT | 10054 |
rs543038704 | in-del | -/AC | 0.0123036 | 0.0774623 | intron-variant | UBA2 | GRCh38.p7 | 19:34450960 | AGATTTAATCTAGAA[-/AC]ACATTTTTAATGTAA | 10054 |
rs543040894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34461768 | TGCCTTGCAGCCTGG[A/T]AGAAGGGAGATTGTC | 10054 |
rs543326239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34454750 | AGGAAAAATTAAGAA[A/G]TTGCTTTTGCTTTTA | 10054 |
rs543365931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444493 | TGCTTTGAACTGTTA[C/T]ATGTGTAGCTTTCAG | 10054 |
rs543415513 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426550 | TGGAGGTTTTTGCTC[C/T]GTGACCCTGGCTGTT | 10054 |
rs543436928 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461741 | AATAAGACAACAGAC[C/G]TTGGCTTGAAGTGCC | 10054 |
rs543469258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34451918 | TTGAACTTGTTAAAC[A/C]GAGCACAGTAGAGGA | 10054 |
rs543578552 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458509 | GAGCCTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 10054 |
rs543605951 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450787 | CGTGTCTCGCTCTGT[C/T]GCCAAGGCTGGAGCG | 10054 |
rs543640507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34438950 | GCGGTGGCTCACACC[C/T]GTAATCCCGGCACTT | 10054 |
rs543657167 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34445502 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 10054 |
rs543739343 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447179 | CATGGGAGAAAGATG[G/T]AGGCTGGGAGGCTAG | 10054 |
rs543748476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34461628 | GTGACCCTTCTGTAC[A/G]GAATACATGTGGTAT | 10054 |
rs543764071 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467793 | TTAAGACTGGGGGAA[A/G]TTCTTATGGAAATTT | 10054 |
rs543842037 | snp | G/T | 6.11733e-05 | 0.00553018 | intron-variant | UBA2 | GRCh38.p7 | 19:34434982 | AGGTAAAGAAAAGTT[G/T]TATTTTTTTAACTTC | 10054 |
rs543856087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447393 | TCCAATCAAGTTGAC[A/C]CTCAGTATTAAGCAT | 10054 |
rs543869369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445294 | ATGCAAGTTTTAAAA[G/T]GTTACCATCTACACT | 10054 |
rs543915253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34446934 | TCTTATCCCTATTGC[A/G]TTTATTTCCTCACTA | 10054 |
rs544173655 | in-del | -/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427527 | CCAGCTGTTTCGGTG[-/T]TTTTTTTTTGTTTGT | 10054 |
rs544238987 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34434254 | GTAGCTACTCTGCAG[A/G]CAGGTACCACCATAC | 10054 |
rs544251169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440385 | ATGTAAGTAGTTTAA[A/G]TTATTCTAAATAATG | 10054 |
rs544380254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463559 | CACATCCCTGATGTC[C/T]CTGTCCAGATTTTGG | 10054 |
rs544380903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34429723 | CGCCTGTGGTCCCAG[C/T]TACCCGGGAGGCTGT | 10054 |
rs544421132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34428745 | CGGGAGGAGACTGTT[C/G]TTTGGGCACGGGGCG | 10054 |
rs544485235 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428215 | CTATGCTGGTGTGGG[A/T]ATAACACCGCCGGTC | 10054 |
rs544494841 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469321 | AAAAATTGACAGCAG[A/T]GACTTGAAAATGATT | 10054 |
rs544519252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436403 | CTCCCTGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 10054 |
rs544589054 | snp | C/G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441889 | TCATGCTACTGCACT[C/G/T]CAACCTGGGGGACAG | 10054 |
rs544644786 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34448437 | CCATCTCTAAAAACG[A/G]AAAAAAAATAGCCAG | 10054 |
rs544707969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456244 | CTCAGCCTCTCAAGT[A/G]GCTGGGATTACTGGC | 10054 |
rs544725271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446893 | TTACAGGCATGAGCC[A/G]TCGTGCCCAGCCCAC | 10054 |
rs544737499 | snp | A/G | 0.000134628 | 0.00820341 | intron-variant | UBA2 | GRCh38.p7 | 19:34454210 | GAAAGTAATGCTTCA[A/G]AATAGTCAATTTGTG | 10054 |
rs544773247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436849 | ATTCTTGGAACCTTA[C/T]TGAATACCATTCTAC | 10054 |
rs544875772 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34428171 | AGGCTAGAAGGCGAC[C/G]CTTAGACTTTTTAGG | 10054 |
rs545042197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446218 | AAAACTTTCTCAGCT[C/G]TTATCAAACTGCCTC | 10054 |
rs545113486 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462418 | CTTTTGAATGTGATG[A/G]TTCCAAGAGGTTTGC | 10054 |
rs545173287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435812 | AGCCTGGGCAACAGA[A/G]TGAGACTCCATCTCA | 10054 |
rs545176184 | snp | C/T | 3.36598e-05 | 0.00410229 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469107 | AAATAATGCCGACGT[C/T]AGTGAAGAAGAGAGA | 10054 |
rs545194838 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436511 | TCTATGTTGGTCAGG[C/G]TGGTCTTCAACTCCT | 10054 |
rs545199288 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427533 | TGTTTCGGTGTTTTT[G/T]TTTGTTTGTTTGTTT | 10054 |
rs545234712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34434647 | GTGTTTCTGTGGGTA[C/T]TTCTCCTGGAGTAAA | 10054 |
rs545296379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34434120 | AAAAGTCAAAATTAC[A/G]TTTATTTTTTAAGGC | 10054 |
rs545331942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34448371 | AGGCTGAGGCGGGAG[G/T]ATCACTTGAGGCCAG | 10054 |
rs545456617 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34428942 | GGATGTTGTGACTTT[A/T]ATTTTGAGGTCCCTG | 10054 |
rs545456911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436337 | AGAATTTCGCTCTTG[C/T]TGCCCAGGCTGCAGT | 10054 |
rs545509450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462647 | AGCCAAAAAAAAAGT[A/G]GGGGGAGACTGAAAA | 10054 |
rs545579638 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | UBA2 | GRCh38.p7 | 19:34434137 | TATTTTTTAAGGCTT[-/G]GGGGGGTCTCACTGT | 10054 |
rs545700152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447706 | CTTTGAACAATAAAT[A/T]TCAGCTTCAGAGTCT | 10054 |
rs545732098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456195 | TCTCGGCTCACTGCA[A/G]CCTCCACCTGCTGGG | 10054 |
rs545848645 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34450689 | ATTAACATGTAGTGT[G/T]TTTGTATTTTCCCTG | 10054 |
rs545852241 | in-del | -/TGTACATTTATTTACAACTACATAA | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34449898 | GTGATTGTCTGTAGT[-/TGTACATTTATTTACAACTACATAA]TGTACATTTATTTGT | 10054 |
rs546045762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465923 | GTGTCTTTTGTTTGA[C/T]TTAAATGTTTCTGAT | 10054 |
rs546071287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465081 | TCCTGAGTCTATAGC[A/C]CAGTTAAGATAGACA | 10054 |
rs546155163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437434 | GGCCAACATGGTGAA[A/G]CCCCATCTCTACTAA | 10054 |
rs546158216 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469439 | CCCTTTGAACAAAGT[G/T]TGTGCATAACCAGTC | 10054 |
rs546257744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437047 | ATCAGAAATGGTGTT[C/T]CAGAGAAAACTCTAA | 10054 |
rs546271525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34468823 | TTGAGTTACATAATG[C/T]TTGTCACAATTTTTT | 10054 |
rs546369373 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444794 | CCTGGGCAACAGAGT[A/G]AGACTTTGTCTCCAA | 10054 |
rs546496782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462898 | TCAGGAGTTGGAGAC[C/G]AGCTTGGCCAATATG | 10054 |
rs546530880 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34469972 | ATTAAAAAAAGAACT[C/T]GGTCGGGCACGGTGG | 10054 |
rs546594031 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440460 | CAAGGAGTATATTGT[A/G]ATATTAGCTAAACTC | 10054 |
rs546663038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34429065 | AACGCGCACCATCTT[C/T]ATACCACCCGAGGAG | 10054 |
rs546719243 | in-del | -/GCTG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435251 | AAAATACAAAAATTA[-/GCTG]GCTGGACATGGTGGC | 10054 |
rs546775830 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468014 | AGGCATGTTAGAGTT[C/T]CCTTGTCACCAGTAT | 10054 |
rs547064994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435989 | AGCGGGCGTGGTGGT[A/G]TGCACCTGTAATCCC | 10054 |
rs547075083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435358 | AGCTGAGATTGCACC[A/G]CTGCCCTCCAGCCTG | 10054 |
rs547092778 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34448493 | CCAGCTACTCAGGAG[G/T]CTGGGACAGGAATAT | 10054 |
rs547166220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34449733 | TTTTTGTTCATGTTT[C/T]TGTGGGTTATTTTTG | 10054 |
rs547180233 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34457353 | GCCTGGCAACAAGAG[C/T]GAAACTCTGCCTCAA | 10054 |
rs547183318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464650 | TTATCAGAAAGACCT[A/G]GAGTCCAGGTGTTTG | 10054 |
rs547188768 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34463080 | CCAGCCTGGACAACA[A/G]AGTGAGACTCTGTCT | 10054 |
rs547237169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437669 | ATAATGAAAGATGAT[G/T]CATTTGATAGTTTTG | 10054 |
rs547249364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437211 | AGGTGATCCGCCTGC[C/G]TTGGCCTCCCAAAGT | 10054 |
rs547352685 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBA2 | GRCh38.p7 | 19:34458553 | GCGACAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 10054 |
rs547456937 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447034 | CAAAGGGGAGTTGAT[A/G]GAGTATTAATTCACA | 10054 |
rs547464657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466205 | GCCAGGTGTGGTGGC[A/G]CGCCTATAGTCCCAG | 10054 |
rs547464866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34457958 | TACATTTTTTTCCCT[C/T]ATTATATAAATGTTA | 10054 |
rs547554994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431086 | TCTTTTCCCTTTGCC[C/T]GTCTCCCAACCTGTT | 10054 |
rs547615357 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34430294 | ATATTTTTATGGCAT[C/T]CAGGGAGTTTCCTGA | 10054 |
rs547678961 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34429766 | GCTTGAGCCTGGGAG[G/T]TCGAGGCTGCAGTGA | 10054 |
rs547691637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459228 | GTGGGTAAATTCTGT[A/G]TTTTTTGACAAATAA | 10054 |
rs547696644 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455893 | GATCCGCCCACCTCG[A/G]CCTCCCAAAGTGCTG | 10054 |
rs547703895 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450995 | TTTTTTAATGTTTAG[A/G]AATGAAAAGTTTTTT | 10054 |
rs547763702 | snp | C/G | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426778 | ACTCCCAGCCATGTT[C/G]AGACATGCTCTGCCT | 10054 |
rs547797512 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34435561 | TCGGCTGCGTGCAGT[C/G]GCTCATGCCTGTAAT | 10054 |
rs547818445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34448673 | AGGTGATAATAATCA[A/G]TTTTGAACTCATTTG | 10054 |
rs547979787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456582 | CTTTTTTTTGAGATG[A/G]AGTCTTGCTCTGTCA | 10054 |
rs547990392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463922 | TTGGATTTTGGTGAA[C/T]GGGACACAAATCAGC | 10054 |
rs547998983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444899 | ATGTGTTGCATTTGG[A/G]GATTTCCATGAGTGA | 10054 |
rs548027850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443412 | ATTGTGTTAAACTTT[A/T]AAGTTTATAGTCATT | 10054 |
rs548038474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442844 | ACTAGTTGGCAAAGC[A/G]TTAATTTTAGGAAGT | 10054 |
rs548062013 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34429899 | CTTGAAAGAGTAATT[C/G]GATTGAAAGAGAAAT | 10054 |
rs548128851 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34436560 | TGCCTCGGCCTCCCA[A/T]AGTGCTGGGATTATA | 10054 |
rs548206188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34457321 | GCATTAAGCCGAGAT[C/T]GCGCCATTGCACTCC | 10054 |
rs548260687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465542 | CTCAGGAGGCTGAGG[C/T]GGGAGAATTGTTTGA | 10054 |
rs548610440 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34458168 | TGTGCCCTTACTCTT[C/G]CCAAATCAGGTTGCA | 10054 |
rs548831952 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34451215 | CTGCTTTCTCATCCC[A/G]CTCCCCTTTAACACT | 10054 |
rs548925335 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469303 | TCCTTTGTTCCAAAG[C/G]GAAAAAATTGACAGC | 10054 |
rs548925496 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437534 | AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG | 10054 |
rs548927992 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462823 | ATACAAAAATTAGGC[C/T]GGGCGTTGTAGCTGT | 10054 |
rs548946612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431829 | ATAGGAACAGAAATA[C/T]TGTAGTAATTCAGTG | 10054 |
rs548975884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432713 | CAGGCGCACGCCACC[A/G]CACTCAGCTAATTTT | 10054 |
rs549114124 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459870 | TGGTCAAGGAAGTGG[C/T]AGGTACAGCAGCGGG | 10054 |
rs549123791 | snp | G/T | 0.0869089 | 0.189476 | intron-variant | UBA2 | GRCh38.p7 | 19:34444054 | TTTTTGTTTTTTTTT[G/T]TTTTTTTTTTTTTTG | 10054 |
rs549206342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34460727 | TGCTGGGGGTCATCA[C/T]ACTTCCATGTTTGGG | 10054 |
rs549215895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440621 | ATAGATGCAAAAATC[C/T]TATGTAAAATATTAG | 10054 |
rs549281107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34466781 | ATCCACATATTTGGT[A/G]TATACATAGTGTATG | 10054 |
rs549298166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34434321 | AAGTCTTGCTTTGTT[A/G]CCCAGGCTGGCCTCG | 10054 |
rs549450346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453161 | ATGGGGATATAATTT[C/T]CCCTATTTAATAGAT | 10054 |
rs549602563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443566 | CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGATTA | 10054 |
rs549607919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431715 | GTAGCTTAACCCTAA[G/T]GCAATTTTCTCACAT | 10054 |
rs549620413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431118 | GGCAAACCCCCACTT[G/T]TTTCTCTTTTTCTTT | 10054 |
rs549765258 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34438257 | ATAAGAAAATGGCTG[C/T]GAATAATATTTAGAT | 10054 |
rs549774942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444034 | TGTGTTTAACATGTG[G/T]TTTTTTTTTGTTTTT | 10054 |
rs549890141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34451113 | CTCAAGCCATCCTCC[C/T]CCCTCAGTCTCCTGA | 10054 |
rs549906253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34458428 | AGCCGGGCGAGGTGG[C/T]GGGCGCCTGTAGTCC | 10054 |
rs550063711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453115 | CTGTGTTGAGTATTC[A/G]GTATTCTTAGTCCTC | 10054 |
rs550066528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437737 | ATAAATTCCTTAAAT[G/T]GTAATTTTAAACTTG | 10054 |
rs550204556 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466364 | AGATCACATTGTAAG[C/T]AGAGGATGTAGAAAT | 10054 |
rs550260556 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34466739 | TCTCTCATTTTTTTT[A/T]AAATAAAAATTAAAA | 10054 |
rs550310618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34452838 | CATATTTTGAAACTT[C/T]GGTTGAATCAGACAT | 10054 |
rs550420486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439618 | GAGGATCCCTTGAGC[C/T]CAGGAGTTTGAGACC | 10054 |
rs550463371 | in-del | -/C | 0.0146672 | 0.084371 | intron-variant | UBA2 | GRCh38.p7 | 19:34456106 | TTTCCTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT | 10054 |
rs550486496 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440772 | TCTCTATTAAAAATA[C/T]AAAATTAGCCGGACA | 10054 |
rs550535164 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463769 | TACTGTGCCTGCCTT[A/C]CTCCTCCTATAAGGA | 10054 |
rs550574144 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427612 | CGCGATCTCGGCTCA[C/T]TGCAACCTCTGCCTC | 10054 |
rs550683560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435307 | GGAGGCTGAGCCAGG[C/T]GAATCACTTGAACCT | 10054 |
rs550711447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34432851 | TGAGCCACTGCACCC[A/G]GCCTGTATCTCCGGC | 10054 |
rs550744635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34441231 | GAGGCTGAGGCGAGC[A/G]GATCACGAGGTCAGG | 10054 |
rs550804512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34428989 | ACGACGCGGGGCGGA[A/G]GATGGCAATGATAGC | 10054 |
rs550832839 | snp | C/T | 0.000529521 | 0.0162628 | utr-variant-5-prime, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428408 | TCCCGCCTCCGCCTC[C/T]GCCGCGGCTCGTGGT | 10054 |
rs551054383 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34447772 | AATAATAAGTTTCAT[C/G]TAAAGGACTCATCTC | 10054 |
rs551154171 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465862 | ATTAGGGTTTTTAAT[A/C]ATATTTTTTAGCTCT | 10054 |
rs551168546 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470354 | AAGAGTACTTTCTAA[A/G]ATAAAGCTCTTCCTG | 10054 |
rs551175735 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437316 | ACACCACTGTGTATT[A/G]AGACTGAAGGTGGCT | 10054 |
rs551176489 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444250 | TTTAGTAGAGACAGG[A/G/T]TTTCACCATGTTAGC | 10054 |
rs551210898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435936 | GACCAGCCTGTCCAA[C/T]ATGGTGAAACCCTGT | 10054 |
rs551279647 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469759 | TTTTCAGTTTGTACC[A/G]CCTGGTATGTCTGTG | 10054 |
rs551359893 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426744 | CTTCCCTTCAGCCCC[A/G]TAACAGCAGTATAAA | 10054 |
rs551445628 | in-del | -/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456405 | AGGCGTGAGCTATTG[-/C]GCCCAGCCTCGATGC | 10054 |
rs551516021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438434 | ACCAGGAGTCGGCGT[C/T]CTGGCACAGCCTTAG | 10054 |
rs551534993 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428378 | CCCCACCCGCTTCCG[G/T]CCGCGGCTCGGTTCT | 10054 |
rs551568967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460994 | TGGCTTTCTGATCTT[C/T]CCTTTCAAAAGTTCA | 10054 |
rs551598954 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427831 | CGTAAGCCACCGCGC[C/T]CGGCAGGTGAAAATC | 10054 |
rs551609299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34434380 | CTCAGCCTCCCAGAA[C/T]GCTGAGATTATGGGC | 10054 |
rs551677303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460188 | TGTGTAGCTCACTAC[C/G]TAACCTGCAGGGAAA | 10054 |
rs551685079 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | UBA2 | GRCh38.p7 | 19:34461596 | GAAACTGGTCAGGAA[-/T]TTTCAGTGGCTTCAG | 10054 |
rs551694277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467546 | TTGGGAGGCCGAGGC[A/G]GGCAGATCGCCTGAG | 10054 |
rs551718985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34455865 | TAGGCTGGTCTCGAA[C/T]TCCTGACCTCATGAT | 10054 |
rs551720810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463743 | AAAGTGCTGAGATTA[C/T]AGATGTGAGCTACTG | 10054 |
rs551778523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439838 | GAAGAAAGAAAGAAA[A/G]AAAGAATGAGAAGGA | 10054 |
rs551898757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34454883 | TTAAAATTTGCTTGG[A/T]CATTTTATAGTCCCC | 10054 |
rs552025893 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469688 | CATTGAAACTTGTTT[C/T]TAAATGTTAGATGGC | 10054 |
rs552053861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456453 | TTTTCATGAAATTTC[A/G]GTTTGAAGGAACAGA | 10054 |
rs552118125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442051 | AGCAGTGTGGGCAAC[A/G]TAGTGAAACCCCATC | 10054 |
rs552278665 | snp | A/G/T | 2.52535e-05 | 0.00355332 | intron-variant | UBA2 | GRCh38.p7 | 19:34451965 | AAATTTCTAATATAT[A/G/T]TATTTTTTTCTTTAG | 10054 |
rs552465875 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445742 | TGCTCCTGGCTTCAT[A/G]TTCACTTTTATTTCT | 10054 |
rs552649760 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437747 | TAAATTGTAATTTTA[A/T]ACTTGAATGTGTATC | 10054 |
rs552654321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436489 | TTTTTAGTAGAGACG[A/G]GGTTTCTCTATGTTG | 10054 |
rs552658195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34429241 | ACACTCGCTTGTTTC[A/G]TTAAAGACGTTAGGA | 10054 |
rs552661548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34454154 | ACCTCTTGTTCTAGT[C/T]GAAAGTCTATAGTAT | 10054 |
rs552719618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467539 | CAACGCTTTGGGAGG[C/T]CGAGGCGGGCAGATC | 10054 |
rs552721810 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34436088 | TCACGCCATTGCACT[C/G]CAGCCTGGGCAACGA | 10054 |
rs552762770 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34445342 | ATCTAAATAGGAGGT[-/AA]AATGAGAGGTGGCTT | 10054 |
rs552766707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34458034 | ACTGTGAAAGGCACT[A/G]TCGTTAACTGGAGAA | 10054 |
rs552773648 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34441835 | CTGAGCCATGAGAGC[C/T]GCTTGAACCTGGGAG | 10054 |
rs552812373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465454 | CCAGCCTGACCAACA[C/T]GGTGAAACCCCGTCT | 10054 |
rs552881127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457481 | ATTGCTTTTATTATT[A/G]TCAGTTTCCCTTAGC | 10054 |
rs553010530 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34453632 | GGGTTCAAGTGATCC[C/T]GCCACCTCAGGCTCC | 10054 |
rs553075602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460355 | CTTGAAGAGTGACTT[C/T]GCCGGTTTCCAATAA | 10054 |
rs553081158 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469367 | GCATTCATTTTGCTA[A/G]AACTGTTAGACACAT | 10054 |
rs553106717 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429270 | GACTGTGCCTTTTGC[A/G]TTGGTGTACGTTGAC | 10054 |
rs553146958 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436379 | ATCTCAGCTCGCCGC[A/C]ACCTCCGTCTCCCTG | 10054 |
rs553168237 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432065 | TGGTTTCTGCTTACA[A/G]AGTGGCATTCTTTTT | 10054 |
rs553215500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34434543 | AGTTATATTAGAATA[A/G]TGGTGAGTTTAGGAA | 10054 |
rs553228874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447301 | GTTTGCTTTTCCCAG[C/T]CCACTGACTCAAATA | 10054 |
rs553258709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34448342 | GCTTACACTTGTAAT[C/T]CTAGCACTTTGGAAG | 10054 |
rs553284229 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465088 | TCTATAGCACAGTTA[A/G]GATAGACATGGCCCC | 10054 |
rs553307965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34446723 | AGGCTATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 10054 |
rs553356971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34462627 | ATAATGAAAAAATGT[C/T]AAAAAGCCAAAAAAA | 10054 |
rs553380554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34436269 | AAATACCTGTGTGCT[C/T]ATACCTCAGTTTTGT | 10054 |
rs553382141 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428507 | GCTGGTGGTGGGGGC[A/G]GGCGGCATCGGCTGC | 10054 |
rs553440191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34442295 | CACTCGAAGGGAAAC[C/T]TAAATAAGCAATAAG | 10054 |
rs553452312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441796 | TGTGGTGGCACACGC[C/T]TGTAGTCCCACCTAC | 10054 |
rs553498579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34456714 | AGGCGGGTGCCACCA[C/T]GCCTGGCTAATTTTT | 10054 |
rs553503390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465029 | GGTGACAAGAGCAAA[A/G]CTCCATCTCAAAAAA | 10054 |
rs553743546 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438193 | ATAAGGATATGGCTG[G/T]ATTCCCCAGACCCAC | 10054 |
rs553744095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463436 | AGTTCTGGAGGCTGG[A/G]ACACCAAGATGAAGG | 10054 |
rs553950255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450145 | ATTGTTATGCTGCTG[G/T]TATATGACATGTATC | 10054 |
rs553983905 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, stop-gained, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34430178 | CCTCCCAAAGTGTTG[G/T]GATTACAGGTATGAG | 10054 |
rs554129871 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBA2 | GRCh38.p7 | 19:34459165 | AGCACAGTGGTGGCA[C/T]AGTATCACAGCAAGC | 10054 |
rs554175648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441725 | CAGGAGTTTGAGAAC[C/T]GCCTGGGCAACATGG | 10054 |
rs554251409 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34447398 | TCAAGTTGACACTCA[G/T]TATTAAGCATCATAA | 10054 |
rs554298309 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441033 | TGGTTTAAACTAGAA[A/T]ATCTGTAAATGTCAT | 10054 |
rs554348597 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446954 | TTTCCTCACTACAGC[C/T]CTTTTCTAAAACATG | 10054 |
rs554432495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437927 | GGGAGTGGTGGGAGA[C/T]GCCTGTAATCCCAGC | 10054 |
rs554434350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34430916 | GATGCTTTGCTTAGG[A/G]TGCACCTTGTGTTCC | 10054 |
rs554452536 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34443669 | CTGGTCTCGAACTCC[A/T]GACTTTGTGATCTGC | 10054 |
rs554660807 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34455948 | CCACTGCGCCCGGCC[C/T]TTTTTTTTTAAACTG | 10054 |
rs554805735 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34436152 | AAATTCTGTTGTCTA[A/G]GAGTCTGGGCTTATA | 10054 |
rs554808663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464308 | ACAGAAAAATTTGAG[A/G]ATTCAGAAATTGGCG | 10054 |
rs554862340 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34428777 | GCCTCCGCTCGCTGG[G/T]CCGGCTCCGGACGCC | 10054 |
rs554902365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436866 | GAATACCATTCTACA[A/G]AAGACTGTTGTGTAT | 10054 |
rs555081375 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447559 | ATCTCCAATCTGTTA[C/T]TTAGCAGATAATTTT | 10054 |
rs555114883 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34431160 | TTCCTCCTCCAGGAG[C/T]ACTTTCCTAAACCTT | 10054 |
rs555232837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443616 | CTGGCTAATTTTTAT[A/G]TTTTTGGTAGAGACG | 10054 |
rs555296212 | snp | A/G | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34450585 | TATGTACACAGATGC[A/G]GGCATTCGTTATACA | 10054 |
rs555308500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34449876 | CTGACTGGCATCCCT[A/G]GGCTCAGTGATTGTC | 10054 |
rs555353435 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433043 | ATGTGTTCTTTATGC[A/G]TTCCCAGGCACTTGC | 10054 |
rs555385756 | in-del | -/CGTG | | | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426468 | TGTACACCTCTGACA[-/CGTG]CACTCCAGTGCTTCC | 10054 |
rs555401696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430805 | ATAAAGATATATCAA[A/G]TAAAGGACTAAAGAT | 10054 |
rs555416590 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436254 | GAGAATAATAGAACA[A/G]AATACCTGTGTGCTC | 10054 |
rs555495671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467668 | GTAGTCCCAGCTACT[C/G]GGGAGGCTGAGGCAG | 10054 |
rs555509401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34451646 | TCCGCCTCCCGGGTT[C/T]GCGCCATTCTCCTGC | 10054 |
rs555540668 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461782 | GAAGAAGGGAGATTG[-/T]CAACAGCTGGATTGA | 10054 |
rs555553781 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34456989 | CCCATCACATCCTTC[C/T]GGTTTCTTTGCCTGC | 10054 |
rs555682625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458048 | TATCGTTAACTGGAG[A/G]AATTAATGTGTTGGT | 10054 |
rs555731270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426299 | TGTGGGTTGGTCTGC[C/T]CTTCCAGGGTCCAGG | 10054 |
rs555742759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466408 | TGTAGCTAAAGAAAT[A/C]ATGTCCAAGAGTTGC | 10054 |
rs556048470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432171 | GGAAATTTATAAAGA[C/T]CTTATATGCTTGCCT | 10054 |
rs556058236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34430771 | TGAAGCTCTCATTTC[A/G]GCTGAGAGATTGTGA | 10054 |
rs556214278 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | UBA2 | GRCh38.p7 | 19:34436724 | CCATGTTTTGAAACT[A/G]TAGAAAGAGAATTAT | 10054 |
rs556228366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443028 | TAGGATAACTTTATT[A/C]ATAAAAGAGAATCTC | 10054 |
rs556231650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465202 | TTATGGGTAGCATCT[A/G]ACAAACATAAAGGGT | 10054 |
rs556238047 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34451586 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 10054 |
rs556250678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458657 | TTTTGCCATCTGGAC[A/G]GGAATTTTTAAGTCA | 10054 |
rs556361946 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460321 | AATCCCCACGGCTTT[C/T]CTGCTTGCTCTAAGG | 10054 |
rs556407188 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434072 | GAGTTTACAACAAGT[A/T]GGGCCAGAAATATCT | 10054 |
rs556409180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465625 | TGGGCGACAGAGGGG[C/G]ACTCCATGTCAGAAA | 10054 |
rs556483580 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446453 | TTTTCGTCTCTGTCC[C/T]GTGTCTCGGATCTTT | 10054 |
rs556548807 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444143 | GCTCACTGCAACCTC[C/T]GCCTTCTGGGTTCAA | 10054 |
rs556556077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444187 | CTCAGGCTCCTGAGT[A/C]GCTGGGATTACAGGC | 10054 |
rs556570104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438539 | AAAATTTCCTTGACA[A/G]CGTAAAACGTAGTTG | 10054 |
rs556600646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445225 | TAAAATTGAATTAAG[C/G]TTCTATGTATATGCC | 10054 |
rs556655504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460302 | TGGGGATGGAACTCA[C/G]GTGAATCCCCACGGC | 10054 |
rs556712913 | snp | C/T | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467540 | AACGCTTTGGGAGGC[C/T]GAGGCGGGCAGATCG | 10054 |
rs556765865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467637 | AAAAATTAGCTGGGC[A/G]TGGCAGCATGCGTCT | 10054 |
rs556838091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438017 | GATTATGCCACTGTA[C/T]TCCAGCCAGGGTGAC | 10054 |
rs556854927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431579 | GAATGAATGACACTT[C/G]GTTACTTCATGTTGT | 10054 |
rs556919390 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427980 | AGCGATTCTTTTATG[A/G]TTTACATTTTAATAC | 10054 |
rs556980710 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427346 | TGTTACTTATTTTTT[C/T]TTTCTACCAGTTTAG | 10054 |
rs557004359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459671 | TTATGACCCAAAAGT[A/G]TCACTTTCCACTTTG | 10054 |
rs557004517 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34438089 | ATCAATAAAATGAAG[A/T]GTATTTGGTTTAGTA | 10054 |
rs557050707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426220 | TTAACCTCTGTTTTT[C/T]TGAGTTGCCTTTTTG | 10054 |
rs557066090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467079 | TAAAAACAAACTGAT[G/T]ATTAGGAACATTGAC | 10054 |
rs557152149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34439384 | ATACTCTGTACTGAT[A/G]ATGATGAAAATGCTA | 10054 |
rs557196179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440037 | ATTTTTAAAAACTTA[C/G]TAAGTGCCCAGTGCG | 10054 |
rs557228617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446671 | CTAGAGTGCAGTGGC[A/C]TGATCTCAGCTTGCT | 10054 |
rs557231392 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435538 | CAGGCATCAAAAATT[G/T]CTTTGTGTCGGCTGC | 10054 |
rs557354199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462548 | TGGAAAAGAACTAGG[A/G]GAAACTGTTAGTATT | 10054 |
rs557503433 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34463211 | GATGCACTCTGGCCT[A/G]TGTGACACGGTGAGA | 10054 |
rs557631279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453379 | CAGGAAAAATACAAA[C/T]CGTAACAGGAAAAAC | 10054 |
rs557695235 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429681 | CGTCTCTACAAAAAA[A/G]GAAAATTAGCGGGGC | 10054 |
rs557732544 | snp | A/T | 8.17946e-05 | 0.00639458 | intron-variant | UBA2 | GRCh38.p7 | 19:34469016 | CTTTTACCCATTTTC[A/T]TTTTCCCTTTTTTCT | 10054 |
rs557738756 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458881 | CAGAGGTGACTGTGC[A/G]GCTGAATGTCCATAA | 10054 |
rs557823026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439283 | AGCCATGTAACTAAG[C/T]GATAAAAATCTTTAT | 10054 |
rs557897068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445460 | TTTTTTTTTTTTGAG[A/G]TGGAGTCTCACTCTT | 10054 |
rs558007776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34452533 | ATTGTCTTTGAATTG[A/G]AATAGTTATTACTAT | 10054 |
rs558043951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34433783 | TAGTCAACATGGTGA[A/C]ACCGTCTCTACCAAA | 10054 |
rs558081433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34468371 | TTTGAGGAAGAGACT[A/G]TCTGGTAGATTTTCC | 10054 |
rs558120203 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427279 | AGAAGCTTTGCTTTG[G/T]AATCTTTACCTGGAG | 10054 |
rs558123542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459562 | TCACCTCTGGAGCTG[A/C]AGCGAGGGAAGAAAT | 10054 |
rs558428445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447343 | TGGCAACACCCTCAC[A/G]CACACACCCAAGACC | 10054 |
rs558441664 | snp | C/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426406 | TGGTGGGCATTCTAG[C/G/T]GGGGAGGAGAGCAGC | 10054 |
rs558676344 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445972 | TTTAAAAGTTTTTTT[G/T]TTCTGTCTTGACTCC | 10054 |
rs558818388 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34435424 | TTAAAATGCTATAAA[C/T]GTGCTCAAAAGACTA | 10054 |
rs558850821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442386 | ACAGATGCTTCTCAG[A/T]TACTTCCCGATAAAC | 10054 |
rs558883925 | snp | C/T | 0.00063709 | 0.0178365 | intron-variant | UBA2 | GRCh38.p7 | 19:34434834 | AACTAATTTTTTTTT[C/T]CCCAAAAACTCATAC | 10054 |
rs558964629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456241 | TGCCTCAGCCTCTCA[A/G]GTAGCTGGGATTACT | 10054 |
rs559034479 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBA2 | GRCh38.p7 | 19:34439376 | AGTTAAAAATACTCT[A/G]TACTGATAATGATGA | 10054 |
rs559110824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34428677 | GGCCCGGAGCCCGGG[A/C]CCGGAGTTGCGGAGC | 10054 |
rs559223574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34452736 | TTTTATCTCATGAAG[C/T]TTGTATGTTCCTGTG | 10054 |
rs559271931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34449115 | TCACTCTGTTGCCAG[A/G]CTGGAGTGCAGTGGT | 10054 |
rs559310788 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426679 | AGACTGTCCCTTTAT[C/G]CAGCTGCCTTCCAGT | 10054 |
rs559331090 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34456881 | GTTTTTAAATTATTT[A/T]AAAAAAATTTTTTAT | 10054 |
rs559358860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446165 | ATTACAGGCATGAAC[C/T]ACTGAGCCTAGCCCC | 10054 |
rs559377703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34433231 | TCTATATGACATATA[A/G]TCCTGATATCAGTTT | 10054 |
rs559470775 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34445558 | ATTCTCCTGCCTCAG[C/T]CTTCCGAGTAGCTGG | 10054 |
rs559601272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432743 | TTGTATTTTAGTAGG[C/T]GGGGTTTCATCATGT | 10054 |
rs559688377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439420 | GAATGTATTGAATGT[A/G]GTGGTTGGCAAAAAG | 10054 |
rs559706131 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470072 | CCAACCTGGTCAACA[G/T]GGTGAAACCCCATCT | 10054 |
rs559816599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435148 | CATACCTGTAATCCC[A/G]GCACTTCGGGAGGCC | 10054 |
rs559832751 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448997 | ATTCATCTCCTTGCC[C/T]TTGTACCCATTTCAC | 10054 |
rs559914117 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34468498 | TTGTTGGACGAGGAG[A/T]TAAAACCACCTTTAG | 10054 |
rs559929396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464413 | AAATGCAAAAATTAG[C/G]CGGGCATAGTGGCAG | 10054 |
rs559975927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447487 | ATCTTCCAAACCAGT[A/G]TCCTTATTTCCATTC | 10054 |
rs559996925 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447533 | TTGAAAGCCAGAAAA[A/G]TCTGAAGTGCATCTC | 10054 |
rs560041108 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34448577 | TTCAGCCTGGGCAGG[A/T]CAAAGAACAGAGGTG | 10054 |
rs560063716 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451356 | TTCTCAACAATCAGG[A/G]ATAGTTATCAAACAG | 10054 |
rs560118536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34428817 | GCGGGCCCCCGCCTC[C/G]CCGGCAGCGCCAATG | 10054 |
rs560242991 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453519 | TTAATGAAACAGCTT[-/T]TTTTTTTTTTTTTTT | 10054 |
rs560461793 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | UBA2 | GRCh38.p7 | 19:34441931 | GTCTCAGAAAAAGAC[A/C]AAAAAAAAAAAAAGA | 10054 |
rs560482286 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBA2 | GRCh38.p7 | 19:34436449 | GGATTACAGGCGTGC[A/G]CCACCACGCCTGGCT | 10054 |
rs560548199 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444448 | AGTAAATAGAGCTGC[A/G]AGTTGTTCCTAGATC | 10054 |
rs560656052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465420 | GAGGCGGGTGGATCA[C/T]GAGGTCAGGAGTTCA | 10054 |
rs560673621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34449244 | CCAGCTGATTTTTGT[A/G]TTTTTAGTAGAGATG | 10054 |
rs560768311 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34436959 | GGAAGTTCTCTGTCT[G/T]CATTGCAGTATGAGT | 10054 |
rs560819958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34434271 | AGGTACCACCATACC[C/T]GGCTAATTTTTTTAT | 10054 |
rs560828724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430438 | TCAGTTTAACAATTT[C/T]GGTATGGCGATTCGA | 10054 |
rs560828912 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436767 | ATTTGCTGGTTGCGT[C/G]TAATTTTTTTTGGCA | 10054 |
rs560831564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440475 | AATATTAGCTAAACT[C/G]TCCCTGAGAAATTTT | 10054 |
rs560878446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34455667 | TTTATCTTTTGAGAC[A/G]GAGTCTAGCTCTGTT | 10054 |
rs560943950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34462812 | CTCTTGTAAAAATAC[A/G]AAAATTAGGCCGGGC | 10054 |
rs561038941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441051 | CTGTAAATGTCATTC[A/G]CTCATTAGGAAATTA | 10054 |
rs561052621 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462831 | ATTAGGCCGGGCGTT[G/T]TAGCTGTAATGCCAG | 10054 |
rs561189584 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428267 | TTTGCAAGAGCCTGC[C/G]GGTCCCCGCGGGCTG | 10054 |
rs561200230 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34451409 | TCCGCTTACTGAGTT[-/A]CTCATTCTCACTAGG | 10054 |
rs561236617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34449194 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 10054 |
rs561240240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441868 | GGAGGTTGAAGTGAA[C/T]GGAGATCATGCTACT | 10054 |
rs561258191 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBA2 | GRCh38.p7 | 19:34465563 | AATTGTTTGAACCGG[A/G]GAGCCGAGTTTGCAG | 10054 |
rs561271100 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34440632 | AATCCTATGTAAAAT[A/G]TTAGCATATCCTGGG | 10054 |
rs561344538 | in-del | -/A | 0.498589 | 0.02652 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470092 | AACCCCATCTCTACT[-/A]AAAAAAAAAAAAAAA | 10054 |
rs561433920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435940 | AGCCTGTCCAACATG[A/G]TGAAACCCTGTCTCT | 10054 |
rs561510478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443829 | ACAGAAGTATTTACT[A/C]TTCTTAAATTATAGC | 10054 |
rs561566140 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34429729 | TGGTCCCAGCTACCC[A/G]GGAGGCTGTGTCAGG | 10054 |
rs561579088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442466 | TGTTGTTTTTTTGAG[A/G]TGGAGTTTCGCTCTT | 10054 |
rs561623381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436418 | GATTCTCCTGCCTCA[A/G]TCTCCCGAGTAGCTG | 10054 |
rs561625919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443419 | TAAACTTTTAAGTTT[A/G]TAGTCATTTATCCGT | 10054 |
rs561651327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430357 | ATACCATTCTTTCAA[A/C]GTATTTTTGAGAAGT | 10054 |
rs561660628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464506 | GAGGTTGCAGTCAGC[C/T]GGGATCGCGCCATTG | 10054 |
rs561688106 | snp | C/T | 0.000335345 | 0.0129445 | intron-variant | UBA2 | GRCh38.p7 | 19:34450393 | TTTAGTCTTGGAACA[C/T]CTAAGCTGGAAATAT | 10054 |
rs561743813 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34458554 | CGACAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 10054 |
rs561843835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438069 | ACCGCCAAAAAGAAA[C/T]GTATATCAATAAAAT | 10054 |
rs561856751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437595 | AACCTGGGCAACGAG[C/T]GAAATTCCGTCTCAG | 10054 |
rs561974865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431651 | TGGTACGTGGGTCAG[A/G]GGGGGCTCTCCGGTT | 10054 |
rs562022795 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447194 | TAGGCTGGGAGGCTA[A/G]GCCAGTCTAGTCTTT | 10054 |
rs562095634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34459817 | GCCTTTCTTCCAGAA[A/G]CTGGTTAGGCAGGAC | 10054 |
rs562210687 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431013 | TTGAAACAAGACAGT[A/T]CCCCCGATCTTTGTT | 10054 |
rs562265070 | snp | A/C | 1.76924e-05 | 0.0029742 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34451985 | TTTTTCTTTAGGAGA[A/C]GAAACGAATGCATCA | 10054 |
rs562299538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34439100 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAA | 10054 |
rs562323795 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBA2 | GRCh38.p7 | 19:34459093 | TTTCTGTCTGTGGTT[C/G]CAGAATAAGTGCCTC | 10054 |
rs562365213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463889 | ATTCTGAGATACTGG[A/G]GATTAGGGTTTCAAC | 10054 |
rs562429573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457819 | GTGTTTTCTAAACTT[C/T]AGTAGAAGCAGGAGC | 10054 |
rs562445002 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444058 | TGTTTTTTTTTTTTT[G/T]TTTTTTTTTTGTCTC | 10054 |
rs562464872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464419 | AAAAATTAGCCGGGC[A/G]TAGTGGCAGGCGCCT | 10054 |
rs562513023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442779 | GTTGTAAAGGTGAAA[A/C]ATCATTGGTGGACCA | 10054 |
rs562776007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437480 | CTGGGTGTGGTGGCA[C/T]GCACCTGTAATCCCA | 10054 |
rs562899250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466567 | AAATTTGTTGTGTAC[C/T]GTCTTTTTTATTATA | 10054 |
rs563033687 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468978 | ATTATAGAAAATACA[A/G]GTGAGCACAGGTAAC | 10054 |
rs563118200 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34465945 | GTTTCTGATGTTTTT[A/G]GGAGTTCATGTACAG | 10054 |
rs563197399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430974 | ATGTTTGGGGGCTAG[A/G]GGAGCGTTATGCTGC | 10054 |
rs563243566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444544 | AGGCAAGGTGGCTCA[C/T]GCCCGTAGTCCCAGC | 10054 |
rs563248986 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34452624 | TTAAAATCATATTTA[A/T]TAGTACTCTGCAGTT | 10054 |
rs563253732 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBA2 | GRCh38.p7 | 19:34464917 | GAGTTTGAGACCAGC[C/G]TGGCCAAAGGCTGGT | 10054 |
rs563284878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459047 | GGCTGTGATTTCCTG[A/G]GTTATTTTGCCTTCT | 10054 |
rs563287332 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454974 | GTTAATGTCTGAGAT[A/C]TTTATGGGTGAGTCT | 10054 |
rs563354196 | snp | C/T | 2.28558e-05 | 0.00338044 | intron-variant | UBA2 | GRCh38.p7 | 19:34451962 | GTGAAATTTCTAATA[C/T]ATATATTTTTTTCTT | 10054 |
rs563418086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34451132 | TCAGTCTCCTGAGTA[G/T]CTGGGACTGTATGCA | 10054 |
rs563491439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460683 | GAGTGGCAGTGTTTG[A/G]TCATGAAGGTGCTCT | 10054 |
rs563510650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446938 | ATCCCTATTGCATTT[A/G]TTTCCTCACTACAGC | 10054 |
rs563612297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438258 | TAAGAAAATGGCTGC[A/G]AATAATATTTAGATA | 10054 |
rs563622442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446348 | AACCGAAAACTCTTT[C/T]TCTTTCTGCTGGAGA | 10054 |
rs563720444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459939 | TGGTATCTCCTGATT[C/T]TTGAGCTTCAAGGTT | 10054 |
rs563837205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467405 | CCCAGGAGTTCGACA[C/T]TGCAGTGAGCCATGA | 10054 |
rs563958018 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445517 | CGATCTCGGCTCACT[A/G]CAGCCCCGCCTCCTG | 10054 |
rs564084533 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34458369 | GACCATCCTGGCTAA[A/C]ACGGTGAAACCCCGT | 10054 |
rs564196443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34465865 | AGGGTTTTTAATCAT[A/G]TTTTTTAGCTCTCTG | 10054 |
rs564201648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444351 | TAAGCAACCGTGCCT[A/C]TCCAAAACAATGTTT | 10054 |
rs564212458 | in-del | -/T | 0.000219315 | 0.0104695 | intron-variant | UBA2 | GRCh38.p7 | 19:34434984 | TAAAGAAAAGTTTTA[-/T]TTTTTTTAACTTCCC | 10054 |
rs564220407 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454792 | TTTACTGAATTCTTC[A/G]AAGAATTCATTGTGC | 10054 |
rs564246279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431669 | GGGCTCTCCGGTTAT[C/T]TTATAAGTATAAAAG | 10054 |
rs564261604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34451737 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 10054 |
rs564293063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453788 | TTGCCTCAACCTACT[A/G]AATTGCTTGAGACTA | 10054 |
rs564489483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34459885 | CAGGTACAGCAGCGG[A/G]TGGTTGCCCCAGTTT | 10054 |
rs564528347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466705 | TCAAGACCAGCCTGG[A/G]CAACATTATGAGACC | 10054 |
rs564583228 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBA2 | GRCh38.p7 | 19:34445508 | GCAGTGGCACGATCT[C/T]GGCTCACTGCAGCCC | 10054 |
rs564618874 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34464483 | GAATCCCTTGAACCC[A/G]AGAGGTGGAGGTTGC | 10054 |
rs564807200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439582 | TGCCTCTAATCCCAG[C/T]ACTGTGGGAGGGTGA | 10054 |
rs564864590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34440213 | TCTGTAGTCCCAGCT[A/T]CTTGGGAGACTGAGC | 10054 |
rs565052436 | snp | A/G | 0.000791612 | 0.0198791 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469116 | CGACGTCAGTGAAGA[A/G]GAGAGAAGCCGCAAG | 10054 |
rs565106596 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439169 | GCCGAGATCGCGCCA[C/T]TGCACTCCAGCTTGG | 10054 |
rs565170429 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441472 | AAAAATAAAAAATAA[A/C]TAAATAGATAAAATT | 10054 |
rs565172899 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427557 | TTTGTTTGTTTGTTT[G/T]TTTGAGACGGAGTCT | 10054 |
rs565211145 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439822 | GATCCTGTCTTAAAA[C/T]GAAGAAAGAAAGAAA | 10054 |
rs565234089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34435244 | CTCTACTAAAAATAC[A/G]AAAATTAGCTGGACA | 10054 |
rs565377170 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465805 | GGAAGGACATGTACA[A/G]TAAAGTGGAAATACC | 10054 |
rs565448384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441186 | CTAGGCCGGGCGAGG[C/T]GGCTCACGCCTGTAA | 10054 |
rs565569436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441814 | TAGTCCCACCTACTC[A/G]GGAGGCTGAGCCATG | 10054 |
rs565743935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34431355 | ACTCCTGGCCTCAAG[A/G]GATCCTCCTACACTG | 10054 |
rs565749584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445816 | ATTGCCCTTGAACCC[C/T]ATAAGCCCCTTTTTC | 10054 |
rs565756812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438397 | GTAATTTTTATTTGG[A/G]CTTGTAAGTCATGTT | 10054 |
rs565818047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34437838 | GGCGGGCGAATCACA[C/T]GAAGTCAGGAGTTCA | 10054 |
rs565823892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444698 | TGTAGTCCCAACTAC[C/T]TGTGAGGTTGAGACG | 10054 |
rs565865975 | snp | A/C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450649 | TCACTTGCTTTTGTC[A/C/T]GTCAGTATAGTTAAC | 10054 |
rs565883515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467435 | ATTGCACCACTGCAC[C/T]GCAGCCTGGGCAACA | 10054 |
rs565899264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34434333 | GTTGCCCAGGCTGGC[C/T]TCGAACTCCTGGCTT | 10054 |
rs565933214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34468317 | TTCATAACCTGTTTT[C/T]TCCCCCCTCACTGAA | 10054 |
rs566015214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446461 | TCTGTCCTGTGTCTC[A/G]GATCTTTTTTTTCTT | 10054 |
rs566098933 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453616 | GCAGCCTCTGCGTCC[C/T]GGGTTCAAGTGATCC | 10054 |
rs566113838 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34457354 | CCTGGCAACAAGAGC[A/G]AAACTCTGCCTCAAG | 10054 |
rs566118660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462918 | TGGCCAATATGGCAA[A/G]ACCCTGTCTCTACTA | 10054 |
rs566132762 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34462262 | AGGCAGAGGCAGGTG[A/C]TAGATTTGAGATTTG | 10054 |
rs566150507 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468466 | CCATGAGTAAGATAG[A/G]TATTCTGCCTTTGAT | 10054 |
rs566193979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34468830 | ACATAATGCTTGTCA[C/T]AATTTTTTGTTTTGA | 10054 |
rs566224676 | in-del | -/CT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445825 | GAACCCCATAAGCCC[-/CT]TTTTCTTGGTGAAAT | 10054 |
rs566519707 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBA2 | GRCh38.p7 | 19:34465269 | AATATTTTCATGAGT[A/G]TACAAACATGCATAG | 10054 |
rs566624870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441447 | GCGACAGAGCGATAC[G/T]CCGTCTCAAAAAAAT | 10054 |
rs566652242 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | UBA2 | GRCh38.p7 | 19:34443003 | TATCCATGAGTTATT[-/A]AACAGTTTTTAGGAT | 10054 |
rs566673861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447864 | CAGGTGACATTTAAG[C/G]CCAAGGCTTGAAAGA | 10054 |
rs566824658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34429091 | AGGAGTGCAAACGCT[A/G]TTTCCACCCTGCTTT | 10054 |
rs566833339 | snp | C/T | 2.45053e-05 | 0.00350029 | intron-variant | UBA2 | GRCh38.p7 | 19:34428583 | CTGGTGAGGGCCGGG[C/T]GCGCGCGCGTGAATG | 10054 |
rs566927590 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34468205 | CATTTCTTTGACCCT[A/G]TGTCTGTGGCATTCT | 10054 |
rs566929670 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442812 | TTAAATTAGCGGCTG[G/T]CTACTATTTTGCACT | 10054 |
rs566952367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436046 | AATCCCTTGAACCGG[C/G]GAAGCGGAGGTTGCG | 10054 |
rs567011814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435397 | ATCAAGCCTCTGTCT[C/T]AAAAAACAAACTTAA | 10054 |
rs567092934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456833 | AAAGTGCTAGAATTA[A/C]AGGAGTGAGCCACCG | 10054 |
rs567094771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464769 | TTCTTCCATAAAACA[A/G]ATCATTTCGTTTGTG | 10054 |
rs567149514 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469365 | AAGCATTCATTTTGC[C/T]AGAACTGTTAGACAC | 10054 |
rs567182743 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466206 | CCAGGTGTGGTGGCG[C/T]GCCTATAGTCCCAGC | 10054 |
rs567207165 | in-del | -/GATT | 0.0321403 | 0.122626 | intron-variant | UBA2 | GRCh38.p7 | 19:34463578 | CCAGATTTTGGGATT[-/GATT]GATTGATTGATTGAT | 10054 |
rs567289868 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435033 | TTGGAGCAGGAGGAA[A/G]TAAACTTTGTATTTA | 10054 |
rs567367231 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426881 | AGCATTTTCCCATTA[A/T]TATTTTTCCCACAAC | 10054 |
rs567381626 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426225 | CTCTGTTTTTCTGAG[A/T]TGCCTTTTTGCCTTT | 10054 |
rs567422479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447284 | ACCCAGATTAAGAGA[A/G]GGTTTGCTTTTCCCA | 10054 |
rs567470503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34454977 | AATGTCTGAGATCTT[C/T]ATGGGTGAGTCTGCT | 10054 |
rs567486162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446674 | GAGTGCAGTGGCATG[A/G]TCTCAGCTTGCTGCA | 10054 |
rs567517385 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34428040 | TGAGTTTCCTGTTCA[C/T]ATCCTTTGCCTATAT | 10054 |
rs567545134 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34430204 | ATGAGCCACCACTCC[C/T]GGTGTAGAGAAATAT | 10054 |
rs567594570 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451475 | ATTATATCTTCAAAT[C/T]TCCCAGTAATCCTAT | 10054 |
rs567603490 | in-del | -/TA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449444 | TTGGCTTATTCTCTA[-/TA]AAGATTAAGGATGCT | 10054 |
rs567624324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34435317 | CCAGGCGAATCACTT[A/G]AACCTGAGAGGCAGA | 10054 |
rs567670286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442129 | GGTCCCAGCTACTTG[C/G]GAGGCTGAGGTGAGA | 10054 |
rs567746732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441252 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 10054 |
rs567806796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447788 | TAAAGGACTCATCTC[C/T]TGGCCTGCATACCCA | 10054 |
rs567847064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436444 | AGCTGGGATTACAGG[C/T]GTGCGCCACCACGCC | 10054 |
rs567864028 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470370 | ATAAAGCTCTTCCTG[C/T]GTGTGGTGGTGGTGC | 10054 |
rs567926381 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469764 | AGTTTGTACCGCCTG[C/G]TATGTCTGTGTAAGA | 10054 |
rs567960411 | snp | C/G | 0.00152014 | 0.0275274 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428443 | CCGCCATGGCACTGT[C/G]GCGGGGGCTGCCCCG | 10054 |
rs567979891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34457322 | CATTAAGCCGAGATC[A/G]CGCCATTGCACTCCA | 10054 |
rs568209928 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430085 | TTTATTTTTTCTATT[A/T]CTTGTAGCCACCAGG | 10054 |
rs568323273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436589 | TAGGTGTGAGCCGCC[A/G]TGCCTGGCACATATC | 10054 |
rs568367187 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453274 | ATTTTTTCTTCTGTT[A/C]TGTGATGCCTCTGAA | 10054 |
rs568463331 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34430611 | TGTAAGCAACCTCAA[C/T]AGACAGTTTTTGTTT | 10054 |
rs568478657 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445563 | CCTGCCTCAGCCTTC[C/T]GAGTAGCTGGGATTA | 10054 |
rs568615525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443094 | TTCAGCAGTAAAGAG[C/G]CATTCTACCATGAAA | 10054 |
rs568625765 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBA2 | GRCh38.p7 | 19:34444055 | TTTTGTTTTTTTTTT[G/T]TTTTTTTTTTTTTGT | 10054 |
rs568688960 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBA2 | GRCh38.p7 | 19:34458522 | GCCGAGATTGCGCCA[C/T]TGCACTCCAGCCTGG | 10054 |
rs568761041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450586 | ATGTACACAGATGCA[A/G]GCATTCGTTATACAC | 10054 |
rs568862357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34448657 | GGGGGAGGGTAGGAG[A/G]AGGTGATAATAATCA | 10054 |
rs568966412 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBA2 | GRCh38.p7 | 19:34463123 | AAAGAAAGAAAATTA[A/G]TTAGGCATGGTGGTG | 10054 |
rs569003227 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBA2 | GRCh38.p7 | 19:34436099 | CACTCCAGCCTGGGC[A/G]ACGAGCGAAACTCTG | 10054 |
rs569078000 | in-del | -/A | 0.449979 | 0.150028 | intron-variant | UBA2 | GRCh38.p7 | 19:34457167 | AACCTGGTCTCTACT[-/A]AAAAAAAAAAAAATA | 10054 |
rs569115327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442093 | TTTAAAAATTAGCAA[A/G]GCATGGTGGCACATG | 10054 |
rs569153016 | in-del | -/A | 0.170084 | 0.236883 | intron-variant | UBA2 | GRCh38.p7 | 19:34440926 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 10054 |
rs569229287 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34464882 | TGGGAGGTCGAGGCG[G/T]GTGGATCACCTGAGA | 10054 |
rs569260876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436495 | GTAGAGACGGGGTTT[C/T]TCTATGTTGGTCAGG | 10054 |
rs569282954 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34430790 | GAGAGATTGTGAAGG[A/T]TAAAGATATATCAAG | 10054 |
rs569381283 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34429250 | TGTTTCATTAAAGAC[C/G]TTAGGACTGTGCCTT | 10054 |
rs569431215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450566 | GTGTTCTGGTGGTCC[A/G]CCCTATGTACACAGA | 10054 |
rs569493984 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34449837 | ATACTTTGTGTGCAT[A/G]TCCCCATGAGCTTGG | 10054 |
rs569537359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34435784 | ACAGTGAGCCAAGAT[A/G]GCACCACACTCCAGC | 10054 |
rs569573450 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465870 | TTTTAATCATATTTT[C/T]TAGCTCTCTGGGAAC | 10054 |
rs569632288 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34444039 | TTAACATGTGTTTTT[G/T]TTTTGTTTTTTTTTT | 10054 |
rs569643444 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450526 | TCCCACACTTCAGAA[A/T]TAGCCACTAATAACA | 10054 |
rs569674802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445234 | ATTAAGCTTCTATGT[A/G]TATGCCTTGTGATGT | 10054 |
rs569674803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453130 | AGTATTCTTAGTCCT[C/T]ACCACACCTTATGAG | 10054 |
rs569736203 | snp | A/C | 0 | 0 | intron-variant | UBA2 | GRCh38.p7 | 19:34452360 | TTCATTTGGGATTCT[A/C]GTGATGTGTTCAGGG | 10054 |
rs569745379 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34466762 | AATTAAAAAAAAAAT[G/T]AGAATCCACATATTT | 10054 |
rs569997766 | snp | C/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427952 | TCACTGCAACCTCCA[C/T]CTCCAGGGTTCAAGC | 10054 |
rs570085143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459387 | CAGAGTTTTGGTTTC[A/T]CTGCGTGTTGGACAG | 10054 |
rs570141636 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453964 | ATTCCGGTGTATACA[A/G]CTGAGTCTCCGGTGC | 10054 |
rs570205428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34439674 | GTCTCTACAAAAAAT[A/G]GAAAAATGAGCCAGG | 10054 |
rs570260381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466606 | GCTTTGAAAATTAGA[A/G]TCCAAGGTGGGTATG | 10054 |
rs570306709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443483 | GTCTTGCTCTGTTGC[C/T]CAGGCCGGAGTGCAG | 10054 |
rs570368012 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBA2 | GRCh38.p7 | 19:34450442 | TATAGCCCTGTTGTT[C/G]CTTGAAAATGATATG | 10054 |
rs570374960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34438568 | TGGAATATAGATGAA[G/T]GAAGTGTTTATATTA | 10054 |
rs570393893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430740 | CCTGCCTGTCATATA[A/G]GAGGGAAAAAATGGG | 10054 |
rs570455696 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34437213 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 10054 |
rs570474414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459335 | GTAGAGCAAAGCCCC[A/G]GTTACCAGCTTTGTA | 10054 |
rs570511580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34442988 | TACTGGAAACTTTTA[C/T]ATCCATGAGTTATTA | 10054 |
rs570556393 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34467919 | TAGCAGGTTGGGGTT[G/T]TGTATGCTTGTTTTA | 10054 |
rs570647319 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34466219 | CGCGCCTATAGTCCC[A/T]GCTGCTTGGGAGGCT | 10054 |
rs570656689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446064 | GGTCTCACCATGTTG[C/G]CCAGGCAGATCTCAA | 10054 |
rs570661491 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448719 | ATTAGAGAAGTGGTT[C/T]TGTAGATAAGTAGAG | 10054 |
rs570785397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34451489 | TCTCCCAGTAATCCT[A/G]TGAGGTACTGAGGTG | 10054 |
rs571028474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34438445 | GCGTCCTGGCACAGC[C/T]TTAGCTATGACTGGT | 10054 |
rs571152961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467618 | CATCTGTACTAAAAA[C/T]ACAAAAAATTAGCTG | 10054 |
rs571171245 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBA2 | GRCh38.p7 | 19:34444095 | GGAGTTTCTCTCTTA[C/T]TGCCCAGGCTGGAGT | 10054 |
rs571190778 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440477 | TATTAGCTAAACTCT[C/T]CCTGAGAAATTTTTA | 10054 |
rs571222665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441849 | CCGCTTGAACCTGGG[A/G]GGCGGAGGTTGAAGT | 10054 |
rs571279441 | snp | A/G | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34469977 | AAAAAGAACTCGGTC[A/G]GGCACGGTGGCTCAT | 10054 |
rs571360828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432801 | CTCAGGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 10054 |
rs571373187 | snp | A/C | 4.66059e-05 | 0.00482709 | intron-variant | UBA2 | GRCh38.p7 | 19:34431977 | TATAAGGGTTTTGTA[A/C]GCCAAATATATAAGC | 10054 |
rs571428294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453978 | AACTGAGTCTCCGGT[A/G]CCTTTGTTTAGGCTG | 10054 |
rs571489655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34461001 | CTGATCTTTCCTTTC[A/T]AAAGTTCAAGCAGTT | 10054 |
rs571539173 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428387 | CTTCCGGCCGCGGCT[C/G]GGTTCTCCCGCCTCC | 10054 |
rs571602455 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427854 | TGAAAATCTTACCAT[C/T]TTGCATGGTTTACAT | 10054 |
rs571603982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460204 | TAACCTGCAGGGAAA[G/T]ACAAAGTAGCAAGAG | 10054 |
rs571614438 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBA2 | GRCh38.p7 | 19:34428630 | GGGCTGGGATTCGGG[C/G]GTTCCGGGGCTCCAG | 10054 |
rs571616348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34434396 | GCTGAGATTATGGGC[A/G]TGAGCCAGTGCTCCT | 10054 |
rs571647914 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435278 | TGGCCGGCGCCTGTA[A/T]TCCCAGCTACTTGGG | 10054 |
rs571724127 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437181 | TAGCCAGGCTGGTCT[C/G]AAACTCCTGACCTCA | 10054 |
rs571783418 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463098 | TGAGACTCTGTCTCA[A/G]AAAAAAAAAAAAGAA | 10054 |
rs571807523 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469707 | ATGTTAGATGGCACT[A/G]TGTATATTAATGTAA | 10054 |
rs571929803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460695 | TTGGTCATGAAGGTG[C/T]TCTTTCAAGGTGACA | 10054 |
rs571982943 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBA2 | GRCh38.p7 | 19:34458362 | AGATCGAGACCATCC[C/T]GGCTAACACGGTGAA | 10054 |
rs572046910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34466429 | CAAGAGTTGCTTTAG[A/G]CCACCAAGCTTTGGA | 10054 |
rs572109093 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34465734 | AGTGGTCCTGCTTCA[G/T]TTGGACACTAGATAT | 10054 |
rs572234504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445418 | CTTCTTCGTTTTCCT[C/G]CTGCTTCTCATCTTC | 10054 |
rs572305839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34432200 | CTTAAGTAAGAAGAT[A/G]TTTTAAACTATGAAA | 10054 |
rs572429009 | in-del | -/A | 0.349233 | 0.229462 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467466 | GCAAGACCATGTCTC[-/A]AAAAAAAAAAAAAAA | 10054 |
rs572468377 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34439499 | TTTACTAAGAATCCA[A/G]TTTAAGTTAGAAAAT | 10054 |
rs572638261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34461512 | AGCTGACTTTTAAAA[A/C]AATGTTTGTTTGTGA | 10054 |
rs572741631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432990 | CTGCCTGATCCTGAT[A/C]ATGTGAGGTGAAGTC | 10054 |
rs572761021 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438997 | TCGGATCACCTGAGC[A/G]CAGGAGTTTGAGACC | 10054 |
rs572788294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34446756 | TGGGATTACAGGTCC[A/G]CCACTATGCCTGGCT | 10054 |
rs572822375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441387 | GTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 10054 |
rs572888489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453688 | TGCGCCACCATGCCT[A/G]GCTAATTTTTTGTGT | 10054 |
rs572906683 | snp | G/T | 0.0126979 | 0.078662 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427528 | CCAGCTGTTTCGGTG[G/T]TTTTTTTTGTTTGTT | 10054 |
rs573006819 | snp | C/T | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34469976 | AAAAAAGAACTCGGT[C/T]GGGCACGGTGGCTCA | 10054 |
rs573027402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34434643 | TTATGTGTTTCTGTG[G/T]GTACTTCTCCTGGAG | 10054 |
rs573058554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441810 | CCTGTAGTCCCACCT[A/G]CTCGGGAGGCTGAGC | 10054 |
rs573090743 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UBA2 | GRCh38.p7 | 19:34440902 | CTGCGCTCCAGCCTG[C/G]GCAACAGAGCAAGAC | 10054 |
rs573155274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34455466 | TGTTGTGTCTGCAGA[C/T]ACTTCGCTTTCTTAC | 10054 |
rs573203865 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34440153 | ACATGGCGAAACCCC[A/G]TCTCTACTATAAATA | 10054 |
rs573204910 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468092 | TATTTTTCCAAATAA[C/T]TGATTGTTTACTGTA | 10054 |
rs573269525 | in-del | -/CTT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456106 | TTTCCTTTTCTTTTT[-/CTT]TTTTTTTTTTTTTTT | 10054 |
rs573273591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463456 | CAAGATGAAGGTGCT[A/G]GCAGGTTTGTTTTAT | 10054 |
rs573283754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462633 | AAAAAATGTTAAAAA[C/G]CCAAAAAAAAAGTGG | 10054 |
rs573330205 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34428166 | ACCCCAGGCTAGAAG[A/G]CGACCCTTAGACTTT | 10054 |
rs573407782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34448366 | TTGGAAGGCTGAGGC[A/G]GGAGGATCACTTGAG | 10054 |
rs573569263 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438541 | AATTTCCTTGACAAC[A/G]TAAAACGTAGTTGGA | 10054 |
rs573615094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456183 | ACAGTGATGTGATCT[C/T]GGCTCACTGCAACCT | 10054 |
rs573622286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459684 | GTGTCACTTTCCACT[G/T]TGGGATCACTTCCTA | 10054 |
rs573634303 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432320 | TCTGACTTCTGTAAT[A/G]TAACACTTGGAATTG | 10054 |
rs573672475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445529 | ACTGCAGCCCCGCCT[C/T]CTGGGTTCAAGTGAT | 10054 |
rs573672619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34453584 | GCTGGAGTGCAGTGG[C/G]ATGATCTTGGCTTAC | 10054 |
rs573684680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34452660 | ATCTTTTGAGATTTG[A/G]TATTATGAACTAATT | 10054 |
rs573698861 | snp | C/T | 3.32646e-05 | 0.00407814 | intron-variant | UBA2 | GRCh38.p7 | 19:34464016 | TATCTAAATTATTCA[C/T]GTTTCCTAGCTAATA | 10054 |
rs573707745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34433211 | GAAAGAGTCAAACCT[G/T]ACTATCTATATGACA | 10054 |
rs573768463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34439398 | TAATGATGAAAATGC[C/T]ATACCAGAATGTATT | 10054 |
rs573771427 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427359 | TTCTTTCTACCAGTT[G/T]AGTAGGTGAAAAACT | 10054 |
rs573802171 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433110 | GCCATCTTTCTGCCA[G/T]TTTGAGATCTTTCTC | 10054 |
rs573831538 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34459356 | CAGCTTTGTATTAAA[A/G]GGTATAAGTAACTTG | 10054 |
rs573889646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447399 | CAAGTTGACACTCAG[C/T]ATTAAGCATCATAAT | 10054 |
rs573896718 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442628 | TAGATACAGGGTTTC[A/G]CCTTGTTGGCCAGGC | 10054 |
rs573917814 | in-del | -/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427374 | TAGTAGGTGAAAAAC[-/T]TTTTTTTTTTTTTGA | 10054 |
rs573952921 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34451058 | AGTGCAGTGGCTGTT[A/C]ACAGGCTGTCATAGC | 10054 |
rs574108322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34441726 | AGGAGTTTGAGAACT[A/G]CCTGGGCAACATGGC | 10054 |
rs574121850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34468434 | TCTCTACTGTGGGTA[C/G]GTTTCCAAGGTTACA | 10054 |
rs574178136 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34455363 | AGGGTCTCCTGTTTT[A/C]AGAGTTCCTACCTTA | 10054 |
rs574214652 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34454725 | AAGCTTCCTGGAAAT[G/T]GCAACAAAAAGGAAA | 10054 |
rs574239313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34462590 | AACGTAGGGAAAGGC[A/G]TTCTAAGCGTTTTCC | 10054 |
rs574326961 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34435609 | CTGAGGTAGGCAGAT[A/G]ACTTGAGGTCAGGAG | 10054 |
rs574558087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34464956 | ATGCCTGTAATCCCA[A/G]AAACTTAGGAGGCAG | 10054 |
rs574583976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34463634 | AAATTTTTTTTGCTG[C/T]TCTGTTGCCTAGCAG | 10054 |
rs574681666 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34436199 | TGAAAACTTTTTAGG[G/T]GTGTATTTGTGAAGT | 10054 |
rs574716958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34428779 | CTCCGCTCGCTGGGC[C/T]GGCTCCGGACGCCGA | 10054 |
rs574730392 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34450007 | GGTGACTTAGGAAGG[A/C]AGGGGCAGTCGGCAG | 10054 |
rs574838333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34456937 | TTGAGCTCACCAACA[A/G]TACTAATTACTGAAC | 10054 |
rs574918245 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446495 | TTCTTTTGTCTGCTT[C/T]CCAACACGCACAGGT | 10054 |
rs574929809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430388 | TTATCTCTGACATTA[A/T]ATCTAGATTCTTACA | 10054 |
rs575003954 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444333 | AAAGTGCTGGGACAG[G/T]CGTAAGCAACCGTGC | 10054 |
rs575024112 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447876 | AAGCCCAAGGCTTGA[A/C]AGAATAAGAGTCAGA | 10054 |
rs575042460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34437380 | TTTGGGAGGCCAAGG[A/C]GGGCGGATCACCTGA | 10054 |
rs575098779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBA2 | GRCh38.p7 | 19:34443630 | TATTTTTGGTAGAGA[C/T]GAGGTTTCACCATGT | 10054 |
rs575102584 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34436886 | CTGTTGTGTATGTCA[G/T]TGCGTATTAAGTTGT | 10054 |
rs575124916 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438115 | TAGTAACACCTAAGA[G/T]TTTTCTGTGTAGGGA | 10054 |
rs575151416 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465149 | GTGCATTTTTGTTCA[C/T]GCTCATTGACATGGT | 10054 |
rs575154493 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBA2 | GRCh38.p7 | 19:34440262 | CCAGTGGGTGGAGAT[C/T]GGGCCACTGCACTCC | 10054 |
rs575214488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34447382 | GCATCTTTCAATCCA[A/G]TCAAGTTGACACTCA | 10054 |
rs575241796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443123 | AAAAAAGTTAATCTT[C/G]TTCATTGCTGAATTT | 10054 |
rs575377218 | snp | G/T | 0.00318978 | 0.0398085 | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34469949 | TGCAGGAATGTCAAA[G/T]TCTTTTCATTAAAAA | 10054 |
rs575391206 | snp | A/G | 1.69032e-05 | 0.00290711 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469127 | AAGAAGAGAGAAGCC[A/G]CAAGAGGAAATTAGA | 10054 |
rs575435858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34435547 | AAAATTTCTTTGTGT[C/T]GGCTGCGTGCAGTGG | 10054 |
rs575484019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34428728 | GGGTTGTGCCCCCCC[C/G]GCGGGAGGAGACTGT | 10054 |
rs575595776 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428204 | TGATGGCGGGCCTAT[A/G]CTGGTGTGGGAATAA | 10054 |
rs575704520 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34456888 | AATTATTTAAAAAAA[A/T]TTTTTTATAGCAGCC | 10054 |
rs575709141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443059 | AGCTTAATACTTTCA[A/G]ATTGTTTGTTAACAC | 10054 |
rs575782246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34429663 | GGCAACATAGAGAAA[C/T]CCCGTCTCTACAAAA | 10054 |
rs575823206 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439177 | CGCGCCACTGCACTC[C/T]AGCTTGGCAACAGAG | 10054 |
rs575823327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450840 | CGCAACCTGGGTTCA[A/G]GCGATTCTCCCGCCT | 10054 |
rs575971118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465237 | TGGTGCTGCCACCTG[C/T]GTCCAGTTATTTTGT | 10054 |
rs576041913 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBA2 | GRCh38.p7 | 19:34449132 | TGGAGTGCAGTGGTG[C/T]GATCTCAGCTGACTG | 10054 |
rs576044527 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34444212 | ACAGGCACCTGCCAC[C/G/T]GCGCCCAGCTAATTT | 10054 |
rs576152718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34460381 | AATAAATAGAAGGGG[A/G]AAGTAAGAGCCTTTA | 10054 |
rs576158094 | snp | A/C | 1.65059e-05 | 0.00287275 | intron-variant | UBA2 | GRCh38.p7 | 19:34443816 | AATGCTTTGTTATAC[A/C]GAAGTATTTACTATT | 10054 |
rs576163233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458331 | GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG | 10054 |
rs576221168 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458426 | TTAGCCGGGCGAGGT[-/G]GCGGGCGCCTGTAGT | 10054 |
rs576224693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465676 | AGGACTGAATGTGAG[A/T]TATTAGTAAGTAGTG | 10054 |
rs576255204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457827 | TAAACTTTAGTAGAA[A/G]CAGGAGCTTGGAGCT | 10054 |
rs576400210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34429475 | ATATTTAAGCAAAAA[C/T]TAGATAAAACTTAAA | 10054 |
rs576437997 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435778 | GAGGTTACAGTGAGC[C/G]AAGATGGCACCACAC | 10054 |
rs576514510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34436279 | GTGCTCATACCTCAG[C/T]TTTGTTTTGGTTTAT | 10054 |
rs576539148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467134 | GTGTGTATTGGTTTG[G/T]TATTGATTGTTGTAA | 10054 |
rs576603575 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450772 | TTTTTTTTTTGAGAC[C/T]GTGTCTCGCTCTGTT | 10054 |
rs576626699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34457741 | ACATTGTAGTCACAA[G/T]ATAAAGGTTTGTGTC | 10054 |
rs576638253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34465076 | CAGATTCCTGAGTCT[A/G]TAGCACAGTTAAGAT | 10054 |
rs576660302 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBA2 | GRCh38.p7 | 19:34432022 | CTTTTTTAAAAAAAA[A/T]GATTTTTCTAGAATT | 10054 |
rs576827840 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466197 | AAAAATTAGCCAGGT[A/G]TGGTGGCGCGCCTAT | 10054 |
rs576959700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34458287 | GAGGCCGGGCGCGGT[C/G]GCTCACGCCTGTAAT | 10054 |
rs577126693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34443672 | GTCTCGAACTCCTGA[C/T]TTTGTGATCTGCCTG | 10054 |
rs577192535 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34450653 | TTGCTTTTGTCAGTC[A/C]GTATAGTTAACTAGT | 10054 |
rs577485125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34431558 | GTAAATACTTGTTAA[C/G]TGAATGAATGAATGA | 10054 |
rs577584992 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426407 | GGTGGGCATTCTAGG[C/G]GGGAGGAGAGCAGCG | 10054 |
rs577595735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34437928 | GGAGTGGTGGGAGAT[A/G]CCTGTAATCCCAGCT | 10054 |
rs577596898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34430953 | CCCTAGAGGTTGACT[A/G]CTGCTATGTTTGGGG | 10054 |
rs577652700 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436456 | AGGCGTGCGCCACCA[C/T]GCCTGGCTAATTTTG | 10054 |
rs577698756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34433180 | AAATAATTTCTTTAA[A/G]ATCTGCTTATGTTTG | 10054 |
rs577707658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34459620 | AAGTTCCTGTTAAAT[C/T]GGCTAGATTTGTGTA | 10054 |
rs577729800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34445963 | GGTCCGTGTTTTAAA[A/G]GTTTTTTTGTTCTGT | 10054 |
rs577764273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34432531 | GAGGTACTTAACACT[G/T]TCTCAGGGCATTTGT | 10054 |
rs577768680 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437626 | CAAAAAGAAAAAAAG[-/A]AAGAGACTGAGGTTA | 10054 |
rs577780930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBA2 | GRCh38.p7 | 19:34445479 | AGTCTCACTCTTGTC[A/G]CCCAGGCTGGAGTGC | 10054 |
rs577787374 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34464691 | ACAGAGGCAAATTCA[C/T]TGTAGTAATTAAACT | 10054 |
rs577813535 | snp | C/G | 1.6519e-05 | 0.00287388 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454331 | TTTCAGTATGAATAT[C/G]AAGAGTAGATTTGAT | 10054 |
rs577878949 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426745 | TTCCCTTCAGCCCCA[C/T]AACAGCAGTATAAAA | 10054 |
rs577883506 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462041 | CCCATTATTTGGTTT[C/T]GCTGGAAGTTGGGGT | 10054 |
rs577939932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467792 | TTTAAGACTGGGGGA[A/G]ATTCTTATGGAAATT | 10054 |
rs577940888 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429356 | GAGATGTTACTGGCC[C/T]TTCGGTGTGAGTTTA | 10054 |
rs578024061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34452542 | GAATTGAAATAGTTA[C/T]TACTATTTCAGAGGT | 10054 |
rs578055568 | snp | C/T | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445009 | TTATAGGGGAACCAA[C/T]GGAAGCCGAAGCCAG | 10054 |
rs578173849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBA2 | GRCh38.p7 | 19:34468387 | TCTGGTAGATTTTCC[A/G]AAATCATAATTTGAA | 10054 |
rs745379510 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460703 | GAAGGTGCTCTTTCA[A/G]GGTGACATTGCTGGG | 10054 |
rs745389280 | snp | C/T | 1.93455e-05 | 0.00311005 | missense, intron-variant | UBA2 | GRCh38.p7 | 19:34460540 | AAGGAACAATCCTAA[C/T]ATCTTCCGAAGAGGG | 10054 |
rs745399004 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445916 | AATTGTTTTTATTGG[G/T]TCTACCTAATTATTG | 10054 |
rs745402973 | snp | C/G | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34443896 | TCTCCTGACAGAGCT[C/G]ACCCTGAAGCTGCCT | 10054 |
rs745466845 | in-del | -/TTT | 0.00452999 | 0.0473759 | intron-variant | UBA2 | GRCh38.p7 | 19:34460452 | TAATATTTTGAATCC[-/TTT]TTTTTTTTTTTGTAG | 10054 |
rs745497716 | snp | G/T | 0.000269651 | 0.0116083 | utr-variant-5-prime, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428423 | CGCCGCGGCTCGTGG[G/T]TGTCCCGCCATGGCA | 10054 |
rs745544916 | snp | A/G | 3.31587e-05 | 0.00407164 | intron-variant | UBA2 | GRCh38.p7 | 19:34444991 | AATAAAATAATGATC[A/G]TTTTATAGGGGAACC | 10054 |
rs745571922 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442068 | AGTGAAACCCCATCA[C/T]TACAAAAAATTTAAA | 10054 |
rs745584657 | in-del | -/TT | 0.00117169 | 0.0241759 | intron-variant | UBA2 | GRCh38.p7 | 19:34454427 | GAAACATACTCATCC[-/TT]TTTTTTTTTTCCCAG | 10054 |
rs745629916 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437900 | TCTCTACTAAAAATA[G/T]GAAAATTAGCTGGGA | 10054 |
rs745679545 | snp | G/T | 1.64776e-05 | 0.00287028 | intron-variant | UBA2 | GRCh38.p7 | 19:34431844 | TTGTAGTAATTCAGT[G/T]TTGTTTATTTTTCCA | 10054 |
rs745729897 | snp | C/G | 1.64836e-05 | 0.0028708 | missense, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458916 | ACTGTTCTCACCTTA[C/G]AAGACAAGGTCAGTG | 10054 |
rs745756264 | snp | A/G | 3.31554e-05 | 0.00407144 | intron-variant | UBA2 | GRCh38.p7 | 19:34450234 | CAATTAGGGATTATG[A/G]GGTTCATGGGATCTG | 10054 |
rs745842934 | in-del | -/TTTT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444045 | TGTGTTTTTTTTTTG[-/TTTT]TTTTTTTTTTTTTTT | 10054 |
rs745852508 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462800 | GCAAAACCTCATCTC[C/T]TGTAAAAATACAAAA | 10054 |
rs745955484 | snp | C/T | 2.91456e-05 | 0.00381732 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34434878 | TCCAGCTGCCCGAAA[C/T]CATGTTAATAGAATG | 10054 |
rs746021824 | snp | A/G | 1.65627e-05 | 0.00287769 | intron-variant | UBA2 | GRCh38.p7 | 19:34466844 | CTTTGCTTTCTAAAT[A/G]GTCATAGCAGTGACC | 10054 |
rs746052345 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429052 | GGTTTACACACGGAA[C/T]GCGCACCATCTTCAT | 10054 |
rs746063947 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443511 | CAGTTGTGCAGTCTC[G/T]GCTCACTGCAACCTC | 10054 |
rs746144921 | snp | C/T | 9.95124e-05 | 0.00705311 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464066 | ATTTGGAATTAGAAA[C/T]GGCAGCCGGCTTCAA | 10054 |
rs746213499 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442238 | CCCTGTCACACACAC[-/A]AAAAAAGATAATCTG | 10054 |
rs746231517 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455426 | TAACACTACTTGGAT[A/G]TTCTCTTTGGATTCC | 10054 |
rs746250684 | in-del | -/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465032 | GACAAGAGCAAAACT[-/C]CATCTCAAAAAAAAA | 10054 |
rs746264777 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431027 | TTCCCCCGATCTTTG[C/T]TTAGTTTTTTTAGTG | 10054 |
rs746271199 | snp | C/T | 1.68261e-05 | 0.00290048 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469104 | TTCAAATAATGCCGA[C/T]GTCAGTGAAGAAGAG | 10054 |
rs746328369 | in-del | -/AA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439207 | GTGAGAATTTGTCTC[-/AA]AAAAAAAAAAAAAAA | 10054 |
rs746352055 | snp | A/G | 1.65203e-05 | 0.002874 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454332 | TTCAGTATGAATATG[A/G]AGAGTAGATTTGATA | 10054 |
rs746370893 | snp | C/G | 1.65778e-05 | 0.002879 | intron-variant | UBA2 | GRCh38.p7 | 19:34433430 | GAGGTTATTTTAATA[C/G]TTTTAATTTCTCAGT | 10054 |
rs746425869 | snp | A/G | 1.66868e-05 | 0.00288845 | intron-variant | UBA2 | GRCh38.p7 | 19:34452186 | AGTACTTACATGTCA[A/G]AAGTGTGTTTTAGTT | 10054 |
rs746427987 | snp | A/G | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34469912 | GCCTGCACAGTTCCT[A/G]TTTCTGCTGCCTTAT | 10054 |
rs746513470 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443729 | AAAGGTGTGAGCCAC[A/T]GCGCCCAGCCAGTTG | 10054 |
rs746523608 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462175 | AGTATTTCACTGCCA[C/T]CTGCCACCAGGGTTT | 10054 |
rs746553086 | snp | A/G | 1.68069e-05 | 0.00289882 | intron-variant | UBA2 | GRCh38.p7 | 19:34458732 | GTATAAAATTACAGC[A/G]CGTTTCCGATTTCTG | 10054 |
rs746704881 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34438683 | TCATCCTAAGCCGAC[C/T]CAGAGAACCTTTCCT | 10054 |
rs746774934 | in-del | -/AT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440638 | ATGTAAAATATTAGC[-/AT]ATCCTGGGAATGGGC | 10054 |
rs746799681 | snp | C/T | 1.82747e-05 | 0.00302275 | intron-variant | UBA2 | GRCh38.p7 | 19:34450385 | GAATACATTTTAGTC[C/T]TGGAACACCTAAGCT | 10054 |
rs746823511 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448275 | AACAGGACTTTGCAT[A/G]TATATGGTGAAGATC | 10054 |
rs746874318 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436760 | ACTTAACATTTGCTG[C/G]TTGCGTCTAATTTTT | 10054 |
rs746961066 | snp | A/G | 0.000115614 | 0.0076022 | intron-variant | UBA2 | GRCh38.p7 | 19:34430536 | ACAGCTCAAACATAC[A/G]TAAACGTTTGTCATT | 10054 |
rs747064318 | snp | A/G | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427616 | ATCTCGGCTCACTGC[A/G]ACCTCTGCCTCCTGG | 10054 |
rs747071507 | snp | C/T | 8.24912e-05 | 0.00642175 | intron-variant | UBA2 | GRCh38.p7 | 19:34431959 | GATTACATTGCAAAG[C/T]TGTATAAGGGTTTTG | 10054 |
rs747088427 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462344 | CGTTGTTAGGCGAGC[A/G]CAAGACTTCACAGGT | 10054 |
rs747092317 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433629 | TCTGCATTTCTACCA[A/G]AAGGTATAAATAGAA | 10054 |
rs747100431 | snp | A/G | 3.32127e-05 | 0.00407495 | intron-variant | UBA2 | GRCh38.p7 | 19:34452163 | GTTCGTTTTGACAAT[A/G]TGTGGCAAGTACTTA | 10054 |
rs747154004 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34428855 | CTTCGTGGGCGTGAA[A/G]CCGCCTCTTATCCTC | 10054 |
rs747227812 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445085 | TAAGGAATGGGCTAA[A/G]TCAACTGGATATGAT | 10054 |
rs747345355 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453840 | AGCCTAAAACAGTTT[C/T]CTTAAATTGCTCGTC | 10054 |
rs747394011 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34452661 | TCTTTTGAGATTTGA[C/T]ATTATGAACTAATTT | 10054 |
rs747513752 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433762 | GTCAGGAGTTCGAGA[C/T]CAACCTAGTCAACAT | 10054 |
rs747515595 | snp | A/G | 1.6795e-05 | 0.0028978 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469097 | AAGATTCTTCAAATA[A/G]TGCCGACGTCAGTGA | 10054 |
rs747564179 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428189 | TAGACTTTTTAGGTC[-/T]GATGGCGGGCCTATG | 10054 |
rs747570802 | snp | C/T | 2.00439e-05 | 0.00316568 | intron-variant | UBA2 | GRCh38.p7 | 19:34469021 | ACCCATTTTCTTTTT[C/T]CCTTTTTTCTGAAAT | 10054 |
rs747597895 | snp | C/T | 6.60317e-05 | 0.00574556 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466878 | GTGATTCTCCTACAG[C/T]GAAGACCTAGGAAAG | 10054 |
rs747633028 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436646 | TCATTTGCTATTCAG[A/G]TATTTTTTCTTTCAG | 10054 |
rs747668801 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455758 | AAGCGATTCTCCTGT[C/T]TCAGCCTCCTCAGTA | 10054 |
rs747795732 | snp | C/T | 1.69864e-05 | 0.00291426 | intron-variant | UBA2 | GRCh38.p7 | 19:34454602 | CCCCCCTTAAAAAAA[C/T]CATTAATTAAAAGTA | 10054 |
rs747845013 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460286 | CATCAGTGGTCAGAT[A/G]TGGGGATGGAACTCA | 10054 |
rs747919067 | snp | A/G | 1.65858e-05 | 0.00287969 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464032 | GTTTCCTAGCTAATA[A/G]TCACAAGAAGTTGTC | 10054 |
rs747976785 | in-del | -/CA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463671 | GTGCAGTGGTACAGT[-/CA]CACGCCTCACTGTGT | 10054 |
rs748083549 | snp | C/T | 2.49616e-05 | 0.00353273 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428558 | GCTCACCGGTTTCTC[C/T]CACATCGACCTGGTG | 10054 |
rs748087413 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461320 | GTGAGGTCCTGATGG[C/T]GATTCAGATGTTAAG | 10054 |
rs748104362 | snp | G/T | 1.74695e-05 | 0.00295541 | intron-variant | UBA2 | GRCh38.p7 | 19:34450370 | CAAAGTCAAGGTAAA[G/T]AATACATTTTAGTCT | 10054 |
rs748155682 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444548 | AAGGTGGCTCACGCC[C/G]GTAGTCCCAGCATTT | 10054 |
rs748157952 | snp | C/G/T | 3.31467e-05 | 0.00407093 | intron-variant | UBA2 | GRCh38.p7 | 19:34466829 | ATTTCTCTGGTGCTC[C/G/T]TTTGCTTTCTAAATA | 10054 |
rs748253801 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457655 | TCTCTTGAGGGATTT[-/A]AGTTCTGTATTCTCA | 10054 |
rs748317475 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34452402 | GTTGACTAGAAAAAT[A/G]ACGTGAATATATTAA | 10054 |
rs748354405 | snp | C/T | 3.6495e-05 | 0.00427155 | intron-variant | UBA2 | GRCh38.p7 | 19:34431947 | GTATGCTATAGTGAT[C/T]ACATTGCAAAGTTGT | 10054 |
rs748434532 | in-del | -/A | 0.000662102 | 0.0181828 | intron-variant | UBA2 | GRCh38.p7 | 19:34451967 | ATTTCTAATATATAT[-/A]TTTTTTTCTTTAGGA | 10054 |
rs748445837 | snp | G/T | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452052 | CAGCAGGTTCTAGAT[G/T]TAAAGAGCTATGCAC | 10054 |
rs748495686 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465699 | AAGTAGTGTATTTCA[C/T]AGTTAGATAATGGAG | 10054 |
rs748498495 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432197 | TGCCTTAAGTAAGAA[G/T]ATATTTTAAACTATG | 10054 |
rs748540736 | snp | A/C | 1.65318e-05 | 0.002875 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466997 | GTGATGATGGAGCTC[A/C]GCCCTCCACCTCCAC | 10054 |
rs748644235 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444853 | AAAAGATGCTGATGA[A/G]TGTGTTATTTTCTTA | 10054 |
rs748704311 | snp | C/G | 2.8913e-05 | 0.00380206 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428528 | CATCGGCTGCGAGCT[C/G]CTCAAGAATCTCGTG | 10054 |
rs748713203 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451946 | GGAATGATGTTAATT[A/G]GTGAAATTTCTAATA | 10054 |
rs748759192 | in-del | -/TT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449067 | ATAAAATATAAATCT[-/TT]TTTTTTTTTTTTTTT | 10054 |
rs748823533 | snp | C/T | 3.31868e-05 | 0.00407336 | intron-variant | UBA2 | GRCh38.p7 | 19:34450218 | TTTTCTTGTATCTTA[C/T]CAATTAGGGATTATG | 10054 |
rs748840070 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468345 | GAAATTAGAAAGGTC[C/T]GTCATCTTCCTTTGA | 10054 |
rs748840513 | snp | C/T | 3.97117e-05 | 0.00445581 | utr-variant-5-prime, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428432 | TCGTGGTTGTCCCGC[C/T]ATGGCACTGTCGCGG | 10054 |
rs748871483 | snp | C/G | 1.83478e-05 | 0.00302879 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469246 | CCTCTAAACAGAACC[C/G]TCTTACTATTTAGTT | 10054 |
rs748901551 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457234 | TAGCTGGGCATGGTG[C/G]TGCATGTTTGTAATC | 10054 |
rs748996487 | snp | G/T | 1.68397e-05 | 0.00290165 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469109 | ATAATGCCGACGTCA[G/T]TGAAGAAGAGAGAAG | 10054 |
rs749023366 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459462 | CTGAGTTGAGGCTAA[G/T]TGGTGGTACACACTT | 10054 |
rs749043633 | snp | C/T | 6.61397e-05 | 0.00575026 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34433360 | TAGCCCTGACTATAA[C/T]GTGGAATTTTTCCGA | 10054 |
rs749117135 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461096 | TAGTAAGGATTGCAT[C/T]GTAGTTATTCCTCCT | 10054 |
rs749140983 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439518 | AAGTTAGAAAATGAA[C/G]CACAGAATACACTTT | 10054 |
rs749161804 | snp | C/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426951 | AGCTTTATACAATTT[C/T]TAGCCACTTGTATTT | 10054 |
rs749175179 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449664 | GATAGTTTCTCAATC[-/T]TACTTGTAATGTTTT | 10054 |
rs749236923 | snp | A/G | 0.000115507 | 0.00759869 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445010 | TATAGGGGAACCAAC[A/G]GAAGCCGAAGCCAGA | 10054 |
rs749290002 | snp | A/G | 2.00082e-05 | 0.00316286 | synonymous-codon, intron-variant | UBA2 | GRCh38.p7 | 19:34460550 | CCTAATATCTTCCGA[A/G]GAGGGAGAGACGGAA | 10054 |
rs749355238 | snp | C/T | 3.30693e-05 | 0.00406615 | intron-variant | UBA2 | GRCh38.p7 | 19:34466860 | GTCATAGCAGTGACC[C/T]GTGTGATTCTCCTAC | 10054 |
rs749383552 | snp | A/G | 1.65734e-05 | 0.00287862 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450336 | GAAACCTCCAGTTCC[A/G]TTGGACTGGGCTGAA | 10054 |
rs749407885 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451696 | GGGACTACAGGCGCC[C/T]GCCACCATGCCTGCA | 10054 |
rs749420719 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446011 | TGTACGTGTGTGGGG[-/T]TTTTTTTGACTCTTT | 10054 |
rs749503700 | snp | C/G/T | 5.68675e-05 | 0.00533208 | intron-variant | UBA2 | GRCh38.p7 | 19:34451978 | ATATATTTTTTTCTT[C/G/T]AGGAGAAGAAACGAA | 10054 |
rs749571435 | snp | A/G | 1.65034e-05 | 0.00287253 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466964 | CTGAAGATGCTGCCA[A/G]AAGCATAACCAATGG | 10054 |
rs749638885 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443587 | GCTGGGATTACAGGC[A/G]TGCGCTACCACGCCT | 10054 |
rs749664920 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437133 | AGCCTGGCTAATTTT[C/T]GCATTTTTGGTAGAG | 10054 |
rs749672380 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34430205 | TGAGCCACCACTCCC[A/G]GTGTAGAGAAATATG | 10054 |
rs749748148 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant | UBA2 | GRCh38.p7 | 19:34438640 | CTCATATCCTGACTT[C/T]ATAGGGTGTGACCGA | 10054 |
rs749748328 | in-del | -/T | 2.00837e-05 | 0.00316883 | intron-variant | UBA2 | GRCh38.p7 | 19:34450408 | CCTAAGCTGGAAATA[-/T]CCTCGCGTAAAGTCT | 10054 |
rs749765724 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442507 | CTGGAGTGCAGTGCA[A/G]CTGCAATCTCTGCCT | 10054 |
rs749801328 | snp | C/T | 7.91233e-05 | 0.00628931 | intron-variant | UBA2 | GRCh38.p7 | 19:34454584 | GTTTGCATTTTTATG[C/T]AACCCCCCTTAAAAA | 10054 |
rs749824524 | in-del | -/GGGTTT | 1.65015e-05 | 0.00287237 | intron-variant | UBA2 | GRCh38.p7 | 19:34431967 | TGCAAAGTTGTATAA[-/GGGTTT]TGTAAGCCAAATATA | 10054 |
rs749994495 | snp | C/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427946 | CTTGGTTCACTGCAA[C/T]CTCCACCTCCAGGGT | 10054 |
rs750004188 | snp | C/G | 1.68491e-05 | 0.00290245 | intron-variant | UBA2 | GRCh38.p7 | 19:34433464 | TCCTCTCTCCCATAT[C/G]AAATTTGTTTACAAA | 10054 |
rs750024144 | in-del | -/TTC | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456104 | TTTTTCCTTTTCTTT[-/TTC]TTTTTTTTTTTTTTT | 10054 |
rs750073044 | snp | G/T | 1.68995e-05 | 0.00290679 | intron-variant | UBA2 | GRCh38.p7 | 19:34445160 | CATGGATAGATGTAT[G/T]GTTGTGCATAGATGT | 10054 |
rs750123534 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426656 | AAGGGGTCTTTACTC[C/T]GTTCTGGAGACTGTC | 10054 |
rs750137889 | snp | C/T | 1.67922e-05 | 0.00289755 | intron-variant | UBA2 | GRCh38.p7 | 19:34463992 | TGCTCTATGAAGATG[C/T]AACTGAAGTATCTAA | 10054 |
rs750143119 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455289 | TAAGCACCAAGTTTA[A/G]GATCATTTTTATGGA | 10054 |
rs750182047 | snp | C/T | 1.65078e-05 | 0.00287291 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452137 | ATGGAGCTGAGCTCA[C/T]ATGGGATAAGGTTCG | 10054 |
rs750201725 | snp | A/G | 1.81549e-05 | 0.00301283 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34451982 | ATTTTTTTCTTTAGG[A/G]GAAGAAACGAATGCA | 10054 |
rs750242782 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453555 | TTGAGACAGGGTCTC[A/T]CTCTGTCACCAAGGC | 10054 |
rs750246887 | snp | A/G | 1.67262e-05 | 0.00289185 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469078 | ATAGTTGATTCAGAT[A/G]AAGAAGATTCTTCAA | 10054 |
rs750303288 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439395 | TGATAATGATGAAAA[C/T]GCTATACCAGAATGT | 10054 |
rs750341722 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433326 | AGTTATTTTGGTGAC[C/T]TTTTTTTATTTTGTT | 10054 |
rs750427035 | snp | C/T | 9.88354e-05 | 0.00702908 | missense, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458830 | CTTGTGCACTGGATC[C/T]TCCCAACCCCAATTG | 10054 |
rs750473545 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438854 | CTTGAAGAGATTGAA[C/T]TCAGGATGTTTAAAT | 10054 |
rs750487163 | snp | C/T | 3.29728e-05 | 0.00406021 | intron-variant | UBA2 | GRCh38.p7 | 19:34438629 | AGTAAATTTTTCTCA[C/T]ATCCTGACTTCATAG | 10054 |
rs750527719 | snp | A/C | 3.69816e-05 | 0.00429993 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454503 | GTAATTGCTGGGTTG[A/C]TAGTATTGGAAGGAT | 10054 |
rs750535068 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431687 | ATAAGTATAAAAGTA[C/T]AATTTTATAAGTGTA | 10054 |
rs750574266 | in-del | -/A | 0.00042892 | 0.0146382 | intron-variant | UBA2 | GRCh38.p7 | 19:34454595 | TATGCAACCCCCCTT[-/A]AAAAAATCATTAATT | 10054 |
rs750636642 | snp | A/T | 1.66585e-05 | 0.00288599 | intron-variant | UBA2 | GRCh38.p7 | 19:34458962 | TTTTCCTTTTGCTTT[A/T]ACAGTATTACTGTGA | 10054 |
rs750698484 | in-del | -/TCTG | 3.30918e-05 | 0.00406753 | intron-variant | UBA2 | GRCh38.p7 | 19:34450246 | ATGGGGTTCATGGGA[-/TCTG]TCTTTCTTTTGTAAG | 10054 |
rs750701216 | snp | C/T | 2.44007e-05 | 0.00349281 | intron-variant | UBA2 | GRCh38.p7 | 19:34428593 | CCGGGCGCGCGCGCG[C/T]GAATGGCGGGCTGTG | 10054 |
rs750861992 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436385 | GCTCGCCGCAACCTC[C/T]GTCTCCCTGGTTCAA | 10054 |
rs751028308 | snp | C/G | 1.66407e-05 | 0.00288446 | intron-variant | UBA2 | GRCh38.p7 | 19:34433308 | AAGATCATGTGGAAG[C/G]CTAGTTATTTTGGTG | 10054 |
rs751039177 | snp | A/T | 1.66252e-05 | 0.00288311 | intron-variant | UBA2 | GRCh38.p7 | 19:34431935 | CAGCATCATGAAGTA[A/T]GCTATAGTGATTACA | 10054 |
rs751100677 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440063 | GTGCGGTGGCTCAGG[A/C]CTGCAATCCCAGCAC | 10054 |
rs751200474 | in-del | -/TTT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449066 | GATAAAATATAAATC[-/TTT]TTTTTTTTTTTTTTT | 10054 |
rs751218794 | snp | G/T | 2.29261e-05 | 0.00338563 | synonymous-codon, intron-variant | UBA2 | GRCh38.p7 | 19:34460490 | GAAAGAAAAATTTGC[G/T]ATGGTAGCACCAGAT | 10054 |
rs751320187 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450842 | CAACCTGGGTTCAAG[C/T]GATTCTCCCGCCTCA | 10054 |
rs751341763 | in-del | -/TTCC | 1.64963e-05 | 0.00287192 | intron-variant | UBA2 | GRCh38.p7 | 19:34438777 | TCAAGTAAGAGTGTA[-/TTCC]TATTTCTTGGCATGC | 10054 |
rs751432630 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444361 | TGCCTATCCAAAACA[A/G]TGTTTTACAAAAAAA | 10054 |
rs751434813 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429919 | GAAAGAGAAATACTT[C/T]AGTATTTTTTGAGAC | 10054 |
rs751456545 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449741 | CATGTTTCTGTGGGT[C/T]ATTTTTGGAGGGGAG | 10054 |
rs751483555 | snp | A/G | 0.000149149 | 0.00863435 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452008 | ATGCATCAGATCAAC[A/G]GAATGAACCCCAGTT | 10054 |
rs751532872 | in-del | -/TTTTTCTTTT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456101 | CTTTTTTTCCTTTTC[-/TTTTTCTTTT]TTTTTTTTTTTTTTG | 10054 |
rs751534707 | snp | C/T | 0.000128444 | 0.00801283 | intron-variant | UBA2 | GRCh38.p7 | 19:34468999 | CACAGGTAACTCCCA[C/T]GCTTTTACCCATTTT | 10054 |
rs751599877 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461762 | TTGAAGTGCCTTGCA[G/T]CCTGGAAGAAGGGAG | 10054 |
rs751647329 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436553 | ATCCACCTGCCTCGG[A/C]CTCCCAAAGTGCTGG | 10054 |
rs751673848 | in-del | -/TG | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470391 | GTGGTGGTGCACATC[-/TG]TGTTCCAGCTACTCA | 10054 |
rs751700754 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443286 | GTTTCTTGAGCAGAG[G/T]TTTTAACATTGAAAT | 10054 |
rs751708679 | snp | A/C | 1.79961e-05 | 0.00299962 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469231 | GATTGAACAGAAATG[A/C]CTCTAAACAGAACCC | 10054 |
rs751716413 | snp | A/T | 4.71999e-05 | 0.00485775 | intron-variant | UBA2 | GRCh38.p7 | 19:34434850 | CCCAAAAACTCATAC[A/T]GTTTGTTTTACTTCC | 10054 |
rs751744479 | in-del | -/GTGAGGGCCGGGCGCGCGCGC | 2.44574e-05 | 0.00349687 | splice-donor-variant | UBA2 | GRCh38.p7 | 19:34428571 | TCCCACATCGACCTG[-/GTGAGGGCCGGGCGCGCGCGC]GTGAATGGCGGGCTG | 10054 |
rs751804943 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438107 | ATTTGGTTTAGTAAC[A/G]CCTAAGATTTTTCTG | 10054 |
rs751851049 | snp | A/G | 2.75547e-05 | 0.00371168 | intron-variant | UBA2 | GRCh38.p7 | 19:34434976 | TCAAAAAGGTAAAGA[A/G]AAGTTTTATTTTTTT | 10054 |
rs751869475 | snp | C/T | 4.9534e-05 | 0.0049764 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454295 | TTTTGTCACCTCTGC[C/T]GCAAACCTCAGGATG | 10054 |
rs751878768 | snp | A/G | 1.66599e-05 | 0.00288611 | intron-variant | UBA2 | GRCh38.p7 | 19:34445126 | TTTTTACCAAGGTTA[A/G]ATTTACTTTTTTTAT | 10054 |
rs751899336 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447850 | GAGGCTTTCTAGAGC[A/C]GGTGACATTTAAGCC | 10054 |
rs752042660 | snp | A/C | 4.76406e-05 | 0.00488037 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428487 | GCGGTGGCCGGGGGC[A/C]GGGTGCTGGTGGTGG | 10054 |
rs752090279 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445438 | TTCTCATCTTCACTT[-/T]TTTTTTTTTTTTTTT | 10054 |
rs752162191 | snp | A/G | 2.30338e-05 | 0.00339358 | intron-variant | UBA2 | GRCh38.p7 | 19:34451961 | AGTGAAATTTCTAAT[A/G]TATATATTTTTTTCT | 10054 |
rs752209821 | snp | A/C/G | 3.33457e-05 | 0.00408313 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452001 | GAAACGAATGCATCA[A/C/G]ATCAACAGAATGAAC | 10054 |
rs752258770 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450211 | AATGACGTTTTCTTG[C/T]ATCTTATCAATTAGG | 10054 |
rs752263306 | snp | G/T | 8.36953e-05 | 0.00646844 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467060 | AATACCCACAAAGCA[G/T]AAGTAAAAACAAACT | 10054 |
rs752267823 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437631 | AAGAAAAAAAGAAGA[C/G]ACTGAGGTTAGGAAT | 10054 |
rs752376577 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431918 | ATCGTTGCCTACCAT[A/G]ACAGCATCATGAAGT | 10054 |
rs752444389 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463935 | AACGGGACACAAATC[A/G]GCCCATAACAGAGGT | 10054 |
rs752539074 | snp | C/T | 3.30098e-05 | 0.00406249 | intron-variant | UBA2 | GRCh38.p7 | 19:34438606 | ATGTTGAGAAACTGC[C/T]ATCATGGAGTAAATT | 10054 |
rs752559941 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442045 | TTTGAGAGCAGTGTG[A/G]GCAACATAGTGAAAC | 10054 |
rs752562007 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456315 | AGACGGTGTTTCACC[A/T]GTTGCCCAGATTGGT | 10054 |
rs752571035 | snp | C/T | 1.64944e-05 | 0.00287175 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466913 | TTGAATTTGAAGTTG[C/T]TGGTGATGCCCCGGA | 10054 |
rs752671356 | snp | C/T | 5.62984e-05 | 0.00530528 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428480 | GGCTGAGGCGGTGGC[C/T]GGGGGCCGGGTGCTG | 10054 |
rs752706786 | in-del | -/T | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467800 | TGGGGGAAATTCTTA[-/T]GGAAATTTCTTACAG | 10054 |
rs752785530 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459149 | TTTGACTGGAATCTG[C/T]AGCACAGTGGTGGCA | 10054 |
rs752831719 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455120 | ATTTCTTCAAAGAGC[A/G]TTTGTGGTTATTATA | 10054 |
rs752840284 | in-del | -/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456145 | GGAATCTTGCTCTCA[-/C]CCAGGCTGGAGTACA | 10054 |
rs752849445 | snp | A/T | 0.000165832 | 0.00910431 | intron-variant | UBA2 | GRCh38.p7 | 19:34452158 | ATAAGGTTCGTTTTG[A/T]CAATGTGTGGCAAGT | 10054 |
rs752903915 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434676 | AATTTGTGATATAAA[A/T]TCTATTTGATATTTT | 10054 |
rs752912878 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34467988 | ACAGGTGCTTGTTAA[G/T]TATGGAATTTAGGCA | 10054 |
rs752948957 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433156 | CCAAAAAGGATAGGA[A/T]TTTGAAGGAAATAAT | 10054 |
rs752957132 | snp | A/G | 1.69735e-05 | 0.00291315 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469170 | TCTCAGTGCAAAGAG[A/G]TCACGTATAGAACAG | 10054 |
rs752978155 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445881 | ATTTGCCTGTTAAAT[A/G]TTTCTAGAGAAATCT | 10054 |
rs753012656 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441251 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 10054 |
rs753102681 | snp | A/G | | | synonymous-codon, intron-variant | UBA2 | GRCh38.p7 | 19:34460562 | CGAAGAGGGAGAGAC[A/G]GAAGGTATCATACAT | 10054 |
rs753103869 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446569 | ATTTCGTCTTATTTC[C/T]TCAGTGGTAACAGAT | 10054 |
rs753181209 | snp | C/T | 3.35368e-05 | 0.00409479 | intron-variant | UBA2 | GRCh38.p7 | 19:34444950 | GTGAGTGAAAAGAGT[C/T]CAGTTCTACATTTAT | 10054 |
rs753350288 | snp | A/G | 1.64991e-05 | 0.00287215 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466893 | TGAAGACCTAGGAAA[A/G]GACGTTGAATTTGAA | 10054 |
rs753410512 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444447 | TAGTAAATAGAGCTG[C/T]GAGTTGTTCCTAGAT | 10054 |
rs753416347 | snp | A/G | 1.78953e-05 | 0.00299121 | intron-variant | UBA2 | GRCh38.p7 | 19:34464153 | GCTATTAGTATTTTA[A/G]TTGTAAGAAATTATT | 10054 |
rs753481860 | snp | C/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34428147 | GTCTTGGCTGGGAGT[C/T]GAAACCCCAGGCTAG | 10054 |
rs753505599 | snp | A/C/G | 7.59068e-05 | 0.00616024 | intron-variant | UBA2 | GRCh38.p7 | 19:34428615 | CGGGCTGTGGTGCGG[A/C/G]GGCTGGGATTCGGGG | 10054 |
rs753550400 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454835 | AAGAAGATGTTTCAA[C/T]TGTTTTTCAATTCTG | 10054 |
rs753573737 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429615 | TTCAATAAACGTTTG[C/T]CATGTATCATTTAAG | 10054 |
rs753581326 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458426 | TTAGCCGGGCGAGGT[A/G]GCGGGCGCCTGTAGT | 10054 |
rs753621172 | snp | C/T | 1.65652e-05 | 0.0028779 | intron-variant | UBA2 | GRCh38.p7 | 19:34434844 | TTTTTTCCCAAAAAC[C/T]CATACTGTTTGTTTT | 10054 |
rs753644005 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440523 | TAGCTTGTGTTATTA[A/G]GCTAGCAATGTCTTT | 10054 |
rs753669396 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429293 | ACGTTGACAAGCCAG[A/T]GCTATTTTGAATCGT | 10054 |
rs753673541 | snp | C/T | 1.66676e-05 | 0.00288679 | intron-variant | UBA2 | GRCh38.p7 | 19:34454254 | AATTGTTTAAATTAT[C/T]GGCAGGATGACCCAT | 10054 |
rs753696890 | snp | C/T | 0.000145465 | 0.0085271 | intron-variant | UBA2 | GRCh38.p7 | 19:34435010 | TTCCCAAATATTTAT[C/T]TGAGACCTTGGAGCA | 10054 |
rs753733125 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468897 | AACAGTATGGAAATA[A/C]GTAATGTGTAAAGTG | 10054 |
rs753765616 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453675 | ACGACTTTAGGTGTG[C/T]GCCACCATGCCTGGC | 10054 |
rs753814042 | snp | A/G | 1.65422e-05 | 0.0028759 | intron-variant | UBA2 | GRCh38.p7 | 19:34443949 | GTTTTATCAGATACT[A/G]TTATCTTTATTTTGT | 10054 |
rs753868994 | snp | A/G | 4.91026e-05 | 0.00495469 | intron-variant | UBA2 | GRCh38.p7 | 19:34460435 | TCTTTAATTACCTAC[A/G]TTAATATTTTGAATC | 10054 |
rs753899663 | in-del | -/CCTGGGTCTCTTTT | 1.65288e-05 | 0.00287474 | intron-variant | UBA2 | GRCh38.p7 | 19:34458937 | AAGGTCAGTGCAAGG[-/CCTGGGTCTCTTTT]CCTTTTGCTTTTACA | 10054 |
rs753923692 | in-del | -/CTTT | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34426701 | CCTTCCAGTCTTCCC[-/CTTT]CTTTATTTTTAACAT | 10054 |
rs753925131 | snp | A/G | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467748 | CCTGGGTGACAGAGC[A/G]AGGCTTCCGGCTCCA | 10054 |
rs753959285 | snp | A/G | 1.65113e-05 | 0.00287322 | intron-variant | UBA2 | GRCh38.p7 | 19:34443802 | ACATGTTTGTTTAGA[A/G]TGCTTTGTTATACAG | 10054 |
rs754004933 | snp | A/G | 2.07985e-05 | 0.00322472 | intron-variant | UBA2 | GRCh38.p7 | 19:34469010 | CCCACGCTTTTACCC[A/G]TTTTCTTTTTCCCTT | 10054 |
rs754027632 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433113 | ATCTTTCTGCCAGTT[C/T]GAGATCTTTCTCTTG | 10054 |
rs754046501 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445731 | GCGTGAGCCACTGCT[C/T]CTGGCTTCATGTTCA | 10054 |
rs754076282 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455655 | CACTTACTTTTTTTT[A/C]TCTTTTGAGACGGAG | 10054 |
rs754163463 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439107 | CAGCTACTCGGGAGG[C/G]TGAGGCAAGAGAATT | 10054 |
rs754220267 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459091 | CTTTTCTGTCTGTGG[G/T]TCCAGAATAAGTGCC | 10054 |
rs754236216 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34438662 | TGTGACCGAGTGTTA[C/T]GAGTGTCATCCTAAG | 10054 |
rs754320292 | snp | A/G | 8.25525e-05 | 0.00642413 | intron-variant | UBA2 | GRCh38.p7 | 19:34430686 | TCTCATACCATTTCT[A/G]TAACTTGATGGAGCT | 10054 |
rs754322990 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441022 | GAATACAAGCATGGT[C/T]TAAACTAGAAAATCT | 10054 |
rs754360341 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458838 | CTGGATCCTCCCAAC[C/T]CCAATTGTTATGTAT | 10054 |
rs754412920 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449066 | GATAAAATATAAATC[-/T]TTTTTTTTTTTTTTT | 10054 |
rs754414395 | in-del | -/TC | 5.59143e-05 | 0.00528716 | intron-variant | UBA2 | GRCh38.p7 | 19:34454566 | AGAACAGTGAGTATT[-/TC]TGTTTGCATTTTTAT | 10054 |
rs754425348 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448259 | ATGGAGGAGTAGACT[A/G]AACAGGACTTTGCAT | 10054 |
rs754508345 | snp | C/T | 1.65734e-05 | 0.00287862 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450337 | AAACCTCCAGTTCCG[C/T]TGGACTGGGCTGAAG | 10054 |
rs754693572 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446987 | TGTATTAGGGTTCTC[C/T]AGAGGGACAGAGCTA | 10054 |
rs754714453 | snp | A/G | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427116 | TTTTTCTTTTTTTTC[A/G]AGACAGGGTCTTGCT | 10054 |
rs754805224 | snp | A/G | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34428157 | GGAGTTGAAACCCCA[A/G]GCTAGAAGGCGACCC | 10054 |
rs754815295 | in-del | -/AAA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466751 | TTTTAAATAAAAATT[-/AAA]AAAAAAATTAGAATC | 10054 |
rs754880010 | snp | A/G | 1.66222e-05 | 0.00288285 | intron-variant | UBA2 | GRCh38.p7 | 19:34464017 | ATCTAAATTATTCAC[A/G]TTTCCTAGCTAATAA | 10054 |
rs754895329 | snp | A/G | 1.82118e-05 | 0.00301754 | intron-variant | UBA2 | GRCh38.p7 | 19:34464159 | AGTATTTTAATTGTA[A/G]GAAATTATTTGAATA | 10054 |
rs754912455 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440698 | CTTGGAAGCTGAAGC[A/G]GGTGGATCACCTGAG | 10054 |
rs754980410 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34467880 | AAATGATAGTTTACT[A/C]GTGTGCAAAGTCAGC | 10054 |
rs755063672 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453949 | GTGAGTGGAATTGAG[A/G]TTCCGGTGTATACAA | 10054 |
rs755068665 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453736 | TTTTGCCACGTTGCC[C/T]GGGCTGGTCACAAAC | 10054 |
rs755107690 | snp | A/G | 1.67189e-05 | 0.00289122 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469079 | TAGTTGATTCAGATG[A/G]AGAAGATTCTTCAAA | 10054 |
rs755118829 | snp | A/T | 1.65463e-05 | 0.00287626 | intron-variant | UBA2 | GRCh38.p7 | 19:34443952 | TTATCAGATACTATT[A/T]TCTTTATTTTGTTGA | 10054 |
rs755129421 | in-del | -/TT | 0.000116101 | 0.00761819 | intron-variant | UBA2 | GRCh38.p7 | 19:34458947 | CAAGGCCTGGGTCTC[-/TT]TTCCTTTTGCTTTTA | 10054 |
rs755148218 | snp | A/G | 3.29853e-05 | 0.00406098 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452024 | GAATGAACCCCAGTT[A/G]GGCCTGAAAGACCAG | 10054 |
rs755235644 | snp | A/T | 2.07282e-05 | 0.00321926 | intron-variant | UBA2 | GRCh38.p7 | 19:34469011 | CCACGCTTTTACCCA[A/T]TTTCTTTTTCCCTTT | 10054 |
rs755274637 | snp | C/G | 9.7326e-05 | 0.00697521 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428388 | TTCCGGCCGCGGCTC[C/G]GTTCTCCCGCCTCCG | 10054 |
rs755317821 | snp | A/C | 4.40131e-05 | 0.00469091 | intron-variant | UBA2 | GRCh38.p7 | 19:34454587 | TGCATTTTTATGCAA[A/C]CCCCCTTAAAAAAAT | 10054 |
rs755335328 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444740 | TGAGCCCAAGAGGTA[C/G]AAGCTACAGTGAGCC | 10054 |
rs755421035 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445779 | TATCTGCTATTAGCA[A/G]TTTGACTGACATGTG | 10054 |
rs755465490 | in-del | -/AT | 7.50854e-05 | 0.00612675 | intron-variant | UBA2 | GRCh38.p7 | 19:34451959 | TTAGTGAAATTTCTA[-/AT]ATATATATTTTTTTC | 10054 |
rs755537849 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441112 | GAGAAAGCATTTGGT[A/G]AAATTTAGCAAATGG | 10054 |
rs755558564 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461948 | CTCCCTGGACAAAGA[A/G]GAGAGCATTTAGACA | 10054 |
rs755571680 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459164 | CAGCACAGTGGTGGC[A/G]CAGTATCACAGCAAG | 10054 |
rs755644321 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446867 | TGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 10054 |
rs755659924 | snp | C/T | 0.000134798 | 0.00820859 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428513 | GGTGGGGGCGGGCGG[C/T]ATCGGCTGCGAGCTC | 10054 |
rs755665902 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446611 | CTTTTTTTTTTCTTT[-/T]CTTTTTTTTTTTTTT | 10054 |
rs755666249 | snp | A/G | 1.66863e-05 | 0.0028884 | intron-variant | UBA2 | GRCh38.p7 | 19:34464006 | GTAACTGAAGTATCT[A/G]AATTATTCACGTTTC | 10054 |
rs755738708 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450314 | TGGACAAACTATGGC[A/G]GAAAAGGAAACCTCC | 10054 |
rs755792693 | snp | C/T | 8.48169e-05 | 0.00651163 | intron-variant | UBA2 | GRCh38.p7 | 19:34445165 | ATAGATGTATTGTTG[C/T]GCATAGATGTATTGT | 10054 |
rs755822209 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460835 | CCTGGGAGCTAACCT[C/T]GTGATGAGAAGACTA | 10054 |
rs755837722 | snp | G/T | 3.30852e-05 | 0.00406712 | intron-variant | UBA2 | GRCh38.p7 | 19:34452150 | CATATGGGATAAGGT[G/T]CGTTTTGACAATGTG | 10054 |
rs755867791 | snp | C/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427439 | CAGTGGTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 10054 |
rs755869466 | snp | A/G | 1.69634e-05 | 0.00291229 | intron-variant | UBA2 | GRCh38.p7 | 19:34431944 | GAAGTATGCTATAGT[A/G]ATTACATTGCAAAGT | 10054 |
rs755881273 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426662 | TCTTTACTCCGTTCT[A/G]GAGACTGTCCCTTTA | 10054 |
rs755883133 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453600 | ATGATCTTGGCTTAC[C/T]GCAGCCTCTGCGTCC | 10054 |
rs756006157 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440206 | GTGGGCATCTGTAGT[C/T]CCAGCTACTTGGGAG | 10054 |
rs756100814 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429039 | CTGGTCACGAGCGGG[C/T]TTACACACGGAACGC | 10054 |
rs756104810 | snp | C/T | 1.65888e-05 | 0.00287996 | intron-variant | UBA2 | GRCh38.p7 | 19:34433329 | TATTTTGGTGACCTT[C/T]TTTTATTTTGTTTTG | 10054 |
rs756178540 | in-del | -/TTCTTT | 1.84327e-05 | 0.00303579 | intron-variant | UBA2 | GRCh38.p7 | 19:34450389 | CATTTTAGTCTTGGA[-/TTCTTT]ACACCTAAGCTGGAA | 10054 |
rs756179504 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465506 | GCTGGGTGTGGTGGC[A/G]TGTGCCTGCAGTCCC | 10054 |
rs756227723 | snp | A/G | 1.648e-05 | 0.0028705 | intron-variant | UBA2 | GRCh38.p7 | 19:34438635 | TTTTTCTCATATCCT[A/G]ACTTCATAGGGTGTG | 10054 |
rs756284694 | snp | A/G | 0.000131976 | 0.00812223 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466926 | TGTTGGTGATGCCCC[A/G]GAAAAAGTGGGGCCC | 10054 |
rs756339885 | in-del | -/A | 0.00042892 | 0.0146382 | intron-variant | UBA2 | GRCh38.p7 | 19:34454594 | TATGCAACCCCCCTT[-/A]AAAAAAATCATTAAT | 10054 |
rs756361325 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451574 | TTTTTTTGAGACAGA[G/T]TCTTGCTCTGTCGCC | 10054 |
rs756459829 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443549 | TGGGTTCAAGCGATT[C/T]TCCTGCCTCAGCTTC | 10054 |
rs756483389 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457452 | TGTTAGCCCAGGTAT[C/T]AATAGTGGTAGCAAT | 10054 |
rs756487858 | snp | A/G | 1.81589e-05 | 0.00301316 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469240 | GAAATGCCTCTAAAC[A/G]GAACCCTCTTACTAT | 10054 |
rs756527148 | snp | A/G | 2.65827e-05 | 0.00364563 | intron-variant | UBA2 | GRCh38.p7 | 19:34454559 | CCAGTGCAGAACAGT[A/G]AGTATTTCTGTTTGC | 10054 |
rs756529151 | snp | C/T | 2.46296e-05 | 0.00350916 | intron-variant | UBA2 | GRCh38.p7 | 19:34428600 | CGCGCGCGTGAATGG[C/T]GGGCTGTGGTGCGGG | 10054 |
rs756644073 | snp | G/T | 1.65509e-05 | 0.00287666 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454353 | AGATTTGATATCAAA[G/T]GTAAGTTATTTGTAC | 10054 |
rs756660822 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437549 | CGGGAGGCAGAGGTT[G/T]TGGTGAGCCTAGATC | 10054 |
rs756702652 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465160 | TTCATGCTCATTGAC[A/G]TGGTGGAACTGTGCC | 10054 |
rs756745389 | snp | A/G | 1.66286e-05 | 0.0028834 | intron-variant | UBA2 | GRCh38.p7 | 19:34433315 | TGTGGAAGGCTAGTT[A/G]TTTTGGTGACCTTTT | 10054 |
rs756797808 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426422 | GGGGAGGAGAGCAGC[A/G]AAAGAGCCAAGAGCA | 10054 |
rs756809102 | snp | C/T | 4.98774e-05 | 0.00499362 | intron-variant | UBA2 | GRCh38.p7 | 19:34444986 | TTGAAAATAAAATAA[C/T]GATCGTTTTATAGGG | 10054 |
rs756812162 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460654 | TTACTGTATGTGATA[C/T]TCAGTATTGCAGAGA | 10054 |
rs756864177 | snp | C/G | 1.98801e-05 | 0.00315272 | missense, intron-variant | UBA2 | GRCh38.p7 | 19:34460506 | ATGGTAGCACCAGAT[C/G]TCCAAATTGAAGATG | 10054 |
rs756881562 | snp | A/T | 2.69002e-05 | 0.00366734 | intron-variant | UBA2 | GRCh38.p7 | 19:34460602 | TCATTCCTCTCATTG[A/T]GGAGACTGCTTGAAG | 10054 |
rs756929438 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455083 | TGTGTCTGGTAATTC[-/T]TTAGGGACCCATTGT | 10054 |
rs757004175 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467254 | GGGAGTATTACTTGA[A/G]GCCAGGAGTTGGAGA | 10054 |
rs757010303 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466293 | GTGAACCGAGATCAC[A/G]CTACTGCACTCTAGC | 10054 |
rs757020110 | snp | C/G | 4.27323e-05 | 0.00462216 | intron-variant | UBA2 | GRCh38.p7 | 19:34469000 | ACAGGTAACTCCCAC[C/G]CTTTTACCCATTTTC | 10054 |
rs757021782 | snp | C/T | 3.96157e-05 | 0.00445043 | intron-variant | UBA2 | GRCh38.p7 | 19:34451974 | ATATATATATTTTTT[C/T]CTTTAGGAGAAGAAA | 10054 |
rs757083534 | in-del | -/T | 3.34403e-05 | 0.00408889 | intron-variant | UBA2 | GRCh38.p7 | 19:34445132 | CAAGGTTAGATTTAC[-/T]TTTTTTTATAATCAT | 10054 |
rs757143338 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451813 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 10054 |
rs757248676 | snp | A/G | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452010 | GCATCAGATCAACAG[A/G]ATGAACCCCAGTTAG | 10054 |
rs757360956 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429943 | TTGAGACAGGGTCTG[A/G]CCCTGTCACCCTGGC | 10054 |
rs757389922 | snp | A/G | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454320 | AGGATGCATATTTTC[A/G]GTATGAATATGAAGA | 10054 |
rs757441495 | in-del | -/GC | 2.44275e-05 | 0.00349473 | intron-variant | UBA2 | GRCh38.p7 | 19:34428581 | CCTGGTGAGGGCCGG[-/GC]GCGCGCGCGCGTGAA | 10054 |
rs757494147 | snp | A/G | 3.29995e-05 | 0.00406185 | intron-variant | UBA2 | GRCh38.p7 | 19:34438610 | TGAGAAACTGCCATC[A/G]TGGAGTAAATTTTTC | 10054 |
rs757550172 | snp | A/G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436363 | GCAGTGCAGTGGCGC[A/G/T]ATCTCAGCTCGCCGC | 10054 |
rs757588307 | snp | C/T | 2.13336e-05 | 0.00326593 | utr-variant-5-prime, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428413 | CCTCCGCCTCCGCCG[C/T]GGCTCGTGGTTGTCC | 10054 |
rs757608217 | snp | G/T | 1.68281e-05 | 0.00290065 | intron-variant | UBA2 | GRCh38.p7 | 19:34445151 | TTTTATAATCATGGA[G/T]AGATGTATTGTTGTG | 10054 |
rs757615525 | snp | A/T | 1.79651e-05 | 0.00299704 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454481 | TGCTATTGCTACTAC[A/T]AATGCAGTAATTGCT | 10054 |
rs757617573 | snp | A/T | 8.3022e-05 | 0.00644237 | intron-variant | UBA2 | GRCh38.p7 | 19:34434860 | CATACTGTTTGTTTT[A/T]CTTCCAGCTGCCCGA | 10054 |
rs757662571 | snp | C/T | 1.80007e-05 | 0.003 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469232 | ATTGAACAGAAATGC[C/T]TCTAAACAGAACCCT | 10054 |
rs757698501 | snp | C/G | 7.3111e-05 | 0.00604567 | intron-variant | UBA2 | GRCh38.p7 | 19:34428589 | AGGGCCGGGCGCGCG[C/G]GCGTGAATGGCGGGC | 10054 |
rs757823032 | snp | C/G | 4.00986e-05 | 0.00447747 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428496 | GGGGGCCGGGTGCTG[C/G]TGGTGGGGGCGGGCG | 10054 |
rs757830545 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437760 | TAAACTTGAATGTGT[A/T]TCAATAAAATGGGCT | 10054 |
rs757856824 | in-del | -/AATGGTACCTGGCTGGGC | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448303 | ATCAGTGGAATAAAA[-/AATGGTACCTGGCTGGGC]ACTGTGGCTTACACT | 10054 |
rs757952367 | snp | A/G | 1.64827e-05 | 0.00287073 | intron-variant | UBA2 | GRCh38.p7 | 19:34431818 | GCAGATTTCAGATAG[A/G]AACAGAAATATTGTA | 10054 |
rs757999125 | snp | A/G | 3.29484e-05 | 0.00405871 | synonymous-codon, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458879 | GCCAGAGGTGACTGT[A/G]CGGCTGAATGTCCAT | 10054 |
rs758022781 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449696 | GTTTTTGTAATAATT[A/G]TGTGGGGGTTTTTAC | 10054 |
rs758046876 | snp | C/T | 3.30142e-05 | 0.00406276 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431926 | CTACCATGACAGCAT[C/T]ATGAAGTATGCTATA | 10054 |
rs758199826 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463945 | AAATCAGCCCATAAC[A/G]GAGGTTTAGCTTTTT | 10054 |
rs758231420 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448453 | AAAAAAAATAGCCAG[C/T]CATGGTGGCCTGAGC | 10054 |
rs758334467 | snp | A/T | 1.6495e-05 | 0.0028718 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466917 | ATTTGAAGTTGTTGG[A/T]GATGCCCCGGAAAAA | 10054 |
rs758413839 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466211 | TGTGGTGGCGCGCCT[A/G]TAGTCCCAGCTGCTT | 10054 |
rs758493188 | snp | A/G | 3.32292e-05 | 0.00407597 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454261 | TAAATTATTGGCAGG[A/G]TGACCCATCTGCAAT | 10054 |
rs758538550 | snp | A/G | 1.88234e-05 | 0.00306779 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428482 | CTGAGGCGGTGGCCG[A/G]GGGCCGGGTGCTGGT | 10054 |
rs758635739 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446530 | CTGTCTTAATCAAAT[G/T]ACATACTGCTCTCCC | 10054 |
rs758685466 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453806 | TTGCTTGAGACTACA[A/G]GCATGAGCCACCATG | 10054 |
rs758714738 | snp | A/G | 4.97847e-05 | 0.00498897 | intron-variant | UBA2 | GRCh38.p7 | 19:34452161 | AGGTTCGTTTTGACA[A/G]TGTGTGGCAAGTACT | 10054 |
rs758763355 | snp | A/T | 1.74014e-05 | 0.00294965 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469205 | AAGAGCTTGATGATG[A/T]CATAGCATTAGATTG | 10054 |
rs758773280 | in-del | -/CC | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433045 | TGTTCTTTATGCGTT[-/CC]CCCAGGCACTTGCTG | 10054 |
rs758774789 | snp | C/T | 2.38735e-05 | 0.00345488 | utr-variant-5-prime, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428396 | GCGGCTCGGTTCTCC[C/T]GCCTCCGCCTCCGCC | 10054 |
rs758869690 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434807 | TGAGTCTGTGTCATC[A/C]TAATTAAAGATAACT | 10054 |
rs758934169 | snp | C/G/T | 0.000161634 | 0.00898849 | intron-variant | UBA2 | GRCh38.p7 | 19:34469019 | TTACCCATTTTCTTT[C/G/T]TCCCTTTTTTCTGAA | 10054 |
rs758939673 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466896 | AGACCTAGGAAAGGA[C/T]GTTGAATTTGAAGTT | 10054 |
rs758971306 | snp | A/G | 1.67691e-05 | 0.00289556 | intron-variant | UBA2 | GRCh38.p7 | 19:34444953 | AGTGAAAAGAGTTCA[A/G]TTCTACATTTATTAC | 10054 |
rs759024942 | snp | A/G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34464781 | ACAAATCATTTCGTT[A/G/T]GTGATTTTGTGGCAA | 10054 |
rs759051596 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431069 | TTCAGAGTCTTAAAA[C/T]ATCTTTTCCCTTTGC | 10054 |
rs759133758 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433428 | GTGAGGTTATTTTAA[C/T]ACTTTTAATTTCTCA | 10054 |
rs759198909 | snp | C/T | 1.68863e-05 | 0.00290566 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34451994 | AGGAGAAGAAACGAA[C/T]GCATCAGATCAACAG | 10054 |
rs759291500 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450018 | AAGGCAGGGGCAGTC[A/G]GCAGTTCAGGGCTCC | 10054 |
rs759293408 | snp | C/T | 1.66693e-05 | 0.00288693 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467049 | GCAGGTTGTTAAATA[C/T]CCACAAAGCAGAAGT | 10054 |
rs759324387 | snp | A/G | 1.64923e-05 | 0.00287156 | intron-variant | UBA2 | GRCh38.p7 | 19:34438772 | ACTTGTTCAAGTAAG[A/G]GTGTATATTTCTTGG | 10054 |
rs759342644 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454426 | TGAAACATACTCATC[C/T]TTTTTTTTTTTTCCC | 10054 |
rs759441108 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435925 | CAGGATTTTGAGACC[A/G]GCCTGTCCAACATGG | 10054 |
rs759449268 | snp | C/T | 1.67609e-05 | 0.00289486 | intron-variant | UBA2 | GRCh38.p7 | 19:34458739 | ATTACAGCACGTTTC[C/T]GATTTCTGCCTGTTA | 10054 |
rs759575438 | snp | A/G | 5.05523e-05 | 0.00502728 | intron-variant | UBA2 | GRCh38.p7 | 19:34435014 | CAAATATTTATTTGA[A/G]ACCTTGGAGCAGGAG | 10054 |
rs759582442 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34438652 | CTTCATAGGGTGTGA[C/T]CGAGTGTTATGAGTG | 10054 |
rs759637646 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445386 | GGTTGTCTTTCCTTC[C/T]CTCACTTTTTACAGA | 10054 |
rs759644129 | snp | A/G | 2.36499e-05 | 0.00343866 | intron-variant | UBA2 | GRCh38.p7 | 19:34460581 | GGTATCATACATTGT[A/G]TTTATTCATTCCTCT | 10054 |
rs759670207 | in-del | -/GTG | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34470372 | AAGCTCTTCCTGCGT[-/GTG]GTGGTGGTGGTGCAC | 10054 |
rs759673886 | snp | A/G | 7.45184e-05 | 0.00610358 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428461 | GGGGGCTGCCCCGGG[A/G]GCTGGCTGAGGCGGT | 10054 |
rs759681034 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434580 | GAAACAGTGTTTTGT[A/G]TAAGGTACAGCAATA | 10054 |
rs759681394 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447554 | AGTGCATCTCCAATC[A/T]GTTATTTAGCAGATA | 10054 |
rs759697496 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435548 | AAATTTCTTTGTGTC[A/G]GCTGCGTGCAGTGGC | 10054 |
rs759724623 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462649 | CCAAAAAAAAAGTGG[A/G]GGGAGACTGAAAATT | 10054 |
rs759726803 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445056 | GAAGATGGTGACATT[A/G]AACGTATTTCTACTA | 10054 |
rs759884034 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446460 | CTCTGTCCTGTGTCT[C/T]GGATCTTTTTTTTCT | 10054 |
rs759893452 | snp | C/T | | | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426259 | TGCTGGTGCCGGGGC[C/T]GGGGCCGGGCCAGGA | 10054 |
rs759909924 | snp | C/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427687 | GATTACAGGCGCACG[C/T]CACCACGCCCGGCTA | 10054 |
rs759973121 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443143 | TTGCTGAATTTCTAT[C/T]CCCTAGATGGGGACT | 10054 |
rs759975403 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461773 | TGCAGCCTGGAAGAA[A/G]GGAGATTGTCAACAG | 10054 |
rs760007459 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458981 | TATTACTGTGATGAC[-/A]AAACAAACACTAGCT | 10054 |
rs760010760 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431911 | AGCTAATATCGTTGC[C/T]TACCATGACAGCATC | 10054 |
rs760095824 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444050 | TTTTTTTTTGTTTTT[G/T]TTTTTTTTTTTTTTT | 10054 |
rs760170347 | snp | G/T | 1.65111e-05 | 0.0028732 | intron-variant | UBA2 | GRCh38.p7 | 19:34431974 | TTGTATAAGGGTTTT[G/T]TAAGCCAAATATATA | 10054 |
rs760204217 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463305 | CCCTGAAGTAGTTTC[A/G]GTAGTTAAGTGTTTT | 10054 |
rs760257983 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442633 | ACAGGGTTTCACCTT[A/G]TTGGCCAGGCTGGTC | 10054 |
rs760329385 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434824 | ATTAAAGATAACTAA[-/T]TTTTTTTTTTCCCAA | 10054 |
rs760350191 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466891 | AGTGAAGACCTAGGA[A/G]AGGACGTTGAATTTG | 10054 |
rs760352818 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435443 | CTCAAAAGACTATGG[A/G]CAAGGAAATCTTTCA | 10054 |
rs760416019 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454692 | TAATTTTTCTGGTTA[C/T]CAAGTGAGTGTGTGT | 10054 |
rs760463123 | snp | A/T | 1.66355e-05 | 0.002884 | intron-variant | UBA2 | GRCh38.p7 | 19:34454396 | ACTAAAACCTTGAAG[A/T]TGTTTTTTAAACAGT | 10054 |
rs760492487 | snp | C/G | 1.68832e-05 | 0.00290539 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469128 | AGAAGAGAGAAGCCG[C/G]AAGAGGAAATTAGAT | 10054 |
rs760541239 | snp | C/T | 1.67379e-05 | 0.00289287 | intron-variant | UBA2 | GRCh38.p7 | 19:34434833 | TAACTAATTTTTTTT[C/T]TCCCAAAAACTCATA | 10054 |
rs760587717 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458151 | CCACAGATTAACATG[C/T]CTGTGCCCTTACTCT | 10054 |
rs760699121 | in-del | -/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440918 | CAACAGAGCAAGACT[-/C]CCATCTCAAAAAAAA | 10054 |
rs760724684 | snp | A/G | 3.35065e-05 | 0.00409293 | intron-variant | UBA2 | GRCh38.p7 | 19:34454243 | GAAACTTGTTAAATT[A/G]TTTAAATTATTGGCA | 10054 |
rs760736874 | snp | A/G | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467737 | ACTCCATCCAGCCTG[A/G]GTGACAGAGCGAGGC | 10054 |
rs760780066 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458831 | TTGTGCACTGGATCC[C/T]CCCAACCCCAATTGT | 10054 |
rs760842516 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446371 | GCTGGAGAGAATCCA[C/T]TTTCGGTAAAGGCTA | 10054 |
rs760868680 | snp | G/T | 5.16009e-05 | 0.00507915 | intron-variant | UBA2 | GRCh38.p7 | 19:34460420 | TAGGATTTCTTATGA[G/T]CTTTAATTACCTACG | 10054 |
rs760888384 | snp | C/T | 4.2725e-05 | 0.00462176 | missense, intron-variant | UBA2 | GRCh38.p7 | 19:34460561 | CCGAAGAGGGAGAGA[C/T]GGAAGGTATCATACA | 10054 |
rs760937953 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442878 | AACATGCCATTGTTG[A/G]GAGTGACTATCAGAG | 10054 |
rs761015183 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459845 | GACGGATTGATTTGA[C/G]CTTATGTTTTGGTCA | 10054 |
rs761037767 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439781 | ACCGAGATAGTGCCA[C/T]TGCACTCCAGCCTGG | 10054 |
rs761111743 | in-del | -/GC | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466203 | TAGCCAGGTGTGGTG[-/GC]GCGCCTATAGTCCCA | 10054 |
rs761125178 | in-del | -/CATAAAAG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34452447 | GTGTAGAGTAGATGT[-/CATAAAAG]ATTCATAGAAGTCAT | 10054 |
rs761131013 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451048 | CCCAGATTAGAGTGC[A/G]GTGGCTGTTCACAGG | 10054 |
rs761132998 | snp | A/G | 1.65061e-05 | 0.00287277 | intron-variant | UBA2 | GRCh38.p7 | 19:34430680 | TATATTTCTCATACC[A/G]TTTCTATAACTTGAT | 10054 |
rs761143821 | snp | C/T | | | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426336 | TGTCACAGTGGCAGC[C/T]AGGAAGGTAGCTCCT | 10054 |
rs761155964 | snp | C/T | 6.37586e-05 | 0.00564581 | intron-variant | UBA2 | GRCh38.p7 | 19:34450414 | CTGGAAATATCCTCG[C/T]GTAAAGTCTTTGTAT | 10054 |
rs761238714 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431906 | CCGAAAGCTAATATC[A/G]TTGCCTACCATGACA | 10054 |
rs761321323 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447601 | TGTGCCAGACACCTC[-/T]TTTAAGTACAGGGGA | 10054 |
rs761370223 | snp | A/T | 3.64651e-05 | 0.0042698 | intron-variant | UBA2 | GRCh38.p7 | 19:34434993 | AGTTTTATTTTTTTA[A/T]CTTCCCAAATATTTA | 10054 |
rs761395192 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440077 | GCCTGCAATCCCAGC[A/T]CTTTGGGAGGCTGAG | 10054 |
rs761397944 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454137 | TGGTCTTTCCCTCAG[C/G]AACCTCTTGTTCTAG | 10054 |
rs761412221 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441618 | ACAGTGTCAACTTGA[C/T]AAATGTTCACAAAAA | 10054 |
rs761569814 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468420 | GTACATTTATTGATT[A/C]TCTACTGTGGGTAGG | 10054 |
rs761579384 | in-del | -/C | 0.000175535 | 0.00936678 | intron-variant | UBA2 | GRCh38.p7 | 19:34454587 | TGCATTTTTATGCAA[-/C]CCCCCTTAAAAAAAT | 10054 |
rs761579972 | snp | C/T | 1.66452e-05 | 0.00288484 | intron-variant | UBA2 | GRCh38.p7 | 19:34433450 | AATTTCTCAGTATTT[C/T]CTCTCTCCCATATCA | 10054 |
rs761597710 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453437 | ACAGCATATGTGAGA[C/G]AGTGGTGCATATGAA | 10054 |
rs761681945 | snp | A/G | 3.38169e-05 | 0.00411185 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469121 | TCAGTGAAGAAGAGA[A/G]AAGCCGCAAGAGGAA | 10054 |
rs761692807 | snp | C/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445033 | AAGCCAGAGCTAGAG[C/G]ATCTAATGAAGATGG | 10054 |
rs761740909 | in-del | -/ACC | 2.10804e-05 | 0.0032465 | intron-variant | UBA2 | GRCh38.p7 | 19:34469006 | AACTCCCACGCTTTT[-/ACC]CATTTTCTTTTTCCC | 10054 |
rs761746096 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458188 | ATCAGGTTGCAGAAG[A/T]ACGCGGAGTCTTATA | 10054 |
rs761861960 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445577 | CCGAGTAGCTGGGAT[G/T]ACAGGTGTGTACCAT | 10054 |
rs761881393 | snp | A/G | 7.85006e-05 | 0.00626452 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428444 | CGCCATGGCACTGTC[A/G]CGGGGGCTGCCCCGG | 10054 |
rs761891474 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438450 | CTGGCACAGCCTTAG[C/G]TATGACTGGTAGATT | 10054 |
rs762048921 | snp | A/G | 3.32287e-05 | 0.00407593 | missense, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464100 | GATGACTTCCTCCAG[A/G]ACTATACTTTATTGA | 10054 |
rs762065525 | snp | C/T | 4.97583e-05 | 0.00498765 | intron-variant | UBA2 | GRCh38.p7 | 19:34458756 | ATTTCTGCCTGTTAT[C/T]TCTCCTCCAAAGATT | 10054 |
rs762279906 | snp | C/G | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450289 | GATGACATCAGGTAT[C/G]TGTTGACAATGGACA | 10054 |
rs762350688 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34464513 | CAGTCAGCCGGGATC[A/G]CGCCATTGCACTCCA | 10054 |
rs762402533 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453224 | CTGAGGATTCACAGC[C/G]AGCCAATAAATACAT | 10054 |
rs762418287 | snp | A/T | 6.95689e-05 | 0.00589742 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469058 | AAGAGCAAGATGACG[A/T]TCTCATAGTTGATTC | 10054 |
rs762442428 | snp | C/T | 1.65187e-05 | 0.00287386 | intron-variant | UBA2 | GRCh38.p7 | 19:34466872 | ACCTGTGTGATTCTC[C/T]TACAGTGAAGACCTA | 10054 |
rs762494992 | snp | C/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34467007 | AGCTCAGCCCTCCAC[C/T]TCCACAGGTGAGTAT | 10054 |
rs762510772 | snp | A/C | | | upstream-variant-2KB, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428324 | GCCTGTGTCTGCCGG[A/C]GGCTGTAGTGCGCAG | 10054 |
rs762546881 | snp | A/C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432702 | AGTTGGGATTACAGG[A/C/T]GCACGCCACCACACT | 10054 |
rs762558651 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34452587 | TCTTGATACAAAAAT[A/G]AGATGTAATTATTCT | 10054 |
rs762565906 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454878 | GGGTTTTAAAATTTG[C/T]TTGGTCATTTTATAG | 10054 |
rs762597512 | snp | C/G | 1.66568e-05 | 0.00288585 | intron-variant | UBA2 | GRCh38.p7 | 19:34433298 | TTATACTGCAAAGAT[C/G]ATGTGGAAGGCTAGT | 10054 |
rs762663503 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431381 | CACTGGCCTCCCAAG[C/T]GCTGGGATTACAGGC | 10054 |
rs762718346 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBA2, PDCD2L | GRCh38.p7 | 19:34426657 | AGGGGTCTTTACTCC[A/G]TTCTGGAGACTGTCC | 10054 |
rs762720345 | snp | A/G | 3.29674e-05 | 0.00405988 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452120 | TTTAGCAGAAAAGGG[A/G]GATGGAGCTGAGCTC | 10054 |
rs762810917 | in-del | -/T | 4.9476e-05 | 0.00497348 | intron-variant | UBA2 | GRCh38.p7 | 19:34438620 | CCATCATGGAGTAAA[-/T]TTTTCTCATATCCTG | 10054 |
rs762868890 | snp | A/G | 4.96463e-05 | 0.00498203 | intron-variant | UBA2 | GRCh38.p7 | 19:34458940 | GTCAGTGCAAGGCCT[A/G]GGTCTCTTTTCCTTT | 10054 |
rs762868955 | snp | G/T | 4.95086e-05 | 0.00497512 | intron-variant | UBA2 | GRCh38.p7 | 19:34438784 | AAGAGTGTATATTTC[G/T]TGGCATGCTTTTCGG | 10054 |
rs762906625 | in-del | -/TTT | 0.000727159 | 0.0190539 | intron-variant | UBA2 | GRCh38.p7 | 19:34454427 | GAAACATACTCATCC[-/TTT]TTTTTTTTTCCCAGC | 10054 |
rs763029692 | snp | A/G | 1.64871e-05 | 0.00287111 | intron-variant | UBA2 | GRCh38.p7 | 19:34443914 | CCTGAAGCTGCCTGT[A/G]AGTAAATTATTTGGC | 10054 |
rs763049513 | snp | C/T | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450270 | CTTTTGTAAGCTTTT[C/T]AAAGATGACATCAGG | 10054 |
rs763134405 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449156 | CTGACTGCACTCTCC[A/G]CCTCCCAGGTTCAAG | 10054 |
rs763154585 | in-del | -/TT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444047 | TGTTTTTTTTTTGTT[-/TT]TTTTTTTTTTTTTTT | 10054 |
rs763205545 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463297 | TTTGGTCCCCCTGAA[A/G]TAGTTTCGGTAGTTA | 10054 |
rs763321155 | snp | C/G | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427850 | CAGGTGAAAATCTTA[C/G]CATTTTGCATGGTTT | 10054 |
rs763410477 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447819 | TTTCAGATGTTGTTA[A/G]GGAGAGGCTTCAGAA | 10054 |
rs763503142 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452127 | GAAAAGGGGGATGGA[A/G]CTGAGCTCATATGGG | 10054 |
rs763517650 | snp | A/G | 0.000500488 | 0.0158112 | intron-variant | UBA2 | GRCh38.p7 | 19:34460589 | ACATTGTATTTATTC[A/G]TTCCTCTCATTGAGG | 10054 |
rs763602744 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434336 | GCCCAGGCTGGCCTC[A/G]AACTCCTGGCTTCAA | 10054 |
rs763642096 | snp | C/T | 3.4706e-05 | 0.00416555 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469060 | GAGCAAGATGACGTT[C/T]TCATAGTTGATTCAG | 10054 |
rs763657983 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431927 | TACCATGACAGCATC[A/G]TGAAGTATGCTATAG | 10054 |
rs763663684 | snp | A/G | 1.66524e-05 | 0.00288547 | intron-variant | UBA2 | GRCh38.p7 | 19:34433303 | CTGCAAAGATCATGT[A/G]GAAGGCTAGTTATTT | 10054 |
rs763706669 | snp | A/T | 1.66521e-05 | 0.00288544 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452002 | AAACGAATGCATCAG[A/T]TCAACAGAATGAACC | 10054 |
rs763715788 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432707 | GGATTACAGGCGCAC[A/G]CCACCACACTCAGCT | 10054 |
rs763826860 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466192 | TACAAAAAAATTAGC[C/G]AGGTGTGGTGGCGCG | 10054 |
rs763840037 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431388 | CTCCCAAGTGCTGGG[A/T]TTACAGGCATGAGCC | 10054 |
rs763845477 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451311 | AAACTTAAAAGATCC[C/T]GGGAGACTTGGGATA | 10054 |
rs763899954 | in-del | -/A | 1.64787e-05 | 0.00287038 | intron-variant | UBA2 | GRCh38.p7 | 19:34438639 | CTCATATCCTGACTT[-/A]CATAGGGTGTGACCG | 10054 |
rs763935686 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458032 | CAACTGTGAAAGGCA[C/T]TATCGTTAACTGGAG | 10054 |
rs764016231 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443220 | GTGTAAACACAAACA[C/T]TATTCTGGTGTTAGA | 10054 |
rs764017152 | snp | C/T | 1.6504e-05 | 0.00287258 | intron-variant | UBA2 | GRCh38.p7 | 19:34438785 | AGAGTGTATATTTCT[C/T]GGCATGCTTTTCGGT | 10054 |
rs764019019 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437883 | AACATGGAAAAACCC[C/G]GTCTCTACTAAAAAT | 10054 |
rs764027474 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465231 | GTTTAGTGGTGCTGC[C/T]ACCTGCGTCCAGTTA | 10054 |
rs764036599 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444213 | CAGGCACCTGCCACC[A/G]CGCCCAGCTAATTTT | 10054 |
rs764038201 | in-del | -/G | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427301 | TACCTGGAGTGTGTT[-/G]GAGTGCTTGTTTCCC | 10054 |
rs764109454 | in-del | -/TTTCTTTTTTTT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446608 | TGACTTTTTTTTTTC[-/TTTCTTTTTTTT]TTTCTTTTTTTTTTT | 10054 |
rs764147602 | snp | C/T | 2.43401e-05 | 0.00348847 | intron-variant | UBA2 | GRCh38.p7 | 19:34428585 | GGTGAGGGCCGGGCG[C/T]GCGCGCGTGAATGGC | 10054 |
rs764196256 | snp | A/G | 3.29739e-05 | 0.00406028 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450280 | CTTTTTAAAGATGAC[A/G]TCAGGTATCTGTTGA | 10054 |
rs764200638 | snp | C/G | 1.87623e-05 | 0.00306281 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428485 | AGGCGGTGGCCGGGG[C/G]CCGGGTGCTGGTGGT | 10054 |
rs764209362 | snp | A/G | 1.74567e-05 | 0.00295433 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469207 | GAGCTTGATGATGTC[A/G]TAGCATTAGATTGAA | 10054 |
rs764241057 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463431 | CTCACAGTTCTGGAG[C/G]CTGGAACACCAAGAT | 10054 |
rs764357463 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446169 | CAGGCATGAACCACT[C/G]AGCCTAGCCCCTAGC | 10054 |
rs764427801 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436375 | CGCGATCTCAGCTCG[C/T]CGCAACCTCCGTCTC | 10054 |
rs764442002 | snp | C/G | 1.65685e-05 | 0.00287819 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454266 | TATTGGCAGGATGAC[C/G]CATCTGCAATGGATT | 10054 |
rs764451159 | snp | A/C | 7.73086e-05 | 0.00621678 | intron-variant | UBA2 | GRCh38.p7 | 19:34460595 | TATTTATTCATTCCT[A/C]TCATTGAGGAGACTG | 10054 |
rs764527151 | snp | C/T | 3.31895e-05 | 0.00407353 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464078 | AAATGGCAGCCGGCT[C/T]CAAGCAGATGACTTC | 10054 |
rs764565555 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443363 | AACCTTGCTTACATT[G/T]CTGTTGAAATTGGGA | 10054 |
rs764571575 | in-del | -/GA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437651 | AGGTTAGGAATATCT[-/GA]GATAATGAAAGATGA | 10054 |
rs764572375 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461907 | AGGGAGTACTCTTGG[A/G]TCAGTTTTTGAAGTA | 10054 |
rs764580337 | in-del | -/GCCGGG | | | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426250 | CCTTTGGGTGCTGGT[-/GCCGGG]GCCGGGGCCGGGGCC | 10054 |
rs764582489 | snp | C/T | 0.000116732 | 0.00763887 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467053 | GTTGTTAAATACCCA[C/T]AAAGCAGAAGTAAAA | 10054 |
rs764590737 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462833 | TAGGCCGGGCGTTGT[A/G]GCTGTAATGCCAGCA | 10054 |
rs764641069 | snp | G/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427918 | TACCCAGCCTGGAGT[G/T]AAGTGGTGCGATCTT | 10054 |
rs764649580 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450075 | CTGCATTTCGCTGTT[C/T]TCAATGTAGAGATTC | 10054 |
rs764754571 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465965 | TTCATGTACAGAAGC[A/G]TGGTGTAGCTTGTAA | 10054 |
rs764800732 | snp | G/T | 6.02755e-05 | 0.00548945 | intron-variant | UBA2 | GRCh38.p7 | 19:34451948 | AATGATGTTAATTAG[G/T]GAAATTTCTAATATA | 10054 |
rs764859905 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431115 | TTTGGCAAACCCCCA[C/T]TTGTTTCTCTTTTTC | 10054 |
rs764899986 | in-del | -/T | 4.68439e-05 | 0.0048394 | intron-variant | UBA2 | GRCh38.p7 | 19:34434851 | CAAAAACTCATACTG[-/T]TTTGTTTTACTTCCA | 10054 |
rs764917517 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429666 | AACATAGAGAAACCC[C/T]GTCTCTACAAAAAAA | 10054 |
rs764921468 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438930 | TTAAATGTAGCTGGC[C/T]GGGTGCGGTGGCTCA | 10054 |
rs764943125 | snp | C/G | | | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426347 | CAGCTAGGAAGGTAG[C/G]TCCTCTCTAGTCCAG | 10054 |
rs764958220 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34452404 | TGACTAGAAAAATAA[C/T]GTGAATATATTAAAG | 10054 |
rs765038738 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443141 | CATTGCTGAATTTCT[A/G]TCCCCTAGATGGGGA | 10054 |
rs765097126 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442014 | CCAAGGCAGGAGGAT[A/T]GCTTGAGCCCAGCAG | 10054 |
rs765118876 | snp | A/G | 6.69534e-05 | 0.00578552 | intron-variant | UBA2 | GRCh38.p7 | 19:34458740 | TTACAGCACGTTTCC[A/G]ATTTCTGCCTGTTAT | 10054 |
rs765154232 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455065 | CTGAATGTGTATTAG[A/T]ATTGTGTCTGGTAAT | 10054 |
rs765166075 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461321 | TGAGGTCCTGATGGC[A/G]ATTCAGATGTTAAGC | 10054 |
rs765172219 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455997 | GTCCGGGTTGGTCCT[A/G]AACTCCTGGGCTCAA | 10054 |
rs765232649 | snp | C/T | 1.64947e-05 | 0.00287177 | intron-variant | UBA2 | GRCh38.p7 | 19:34438774 | TTGTTCAAGTAAGAG[C/T]GTATATTTCTTGGCA | 10054 |
rs765273348 | snp | C/T | 1.6552e-05 | 0.00287676 | intron-variant | UBA2 | GRCh38.p7 | 19:34443953 | TATCAGATACTATTA[C/T]CTTTATTTTGTTGAT | 10054 |
rs765338415 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34428581 | ACCTGGTGAGGGCCG[C/G]GCGCGCGCGCGTGAA | 10054 |
rs765342293 | snp | A/G | 2.39736e-05 | 0.00346211 | intron-variant | UBA2 | GRCh38.p7 | 19:34460585 | TCATACATTGTATTT[A/G]TTCATTCCTCTCATT | 10054 |
rs765468877 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461803 | GCTGGATTGAGCATC[A/G]TCCAAGGAAAACTAG | 10054 |
rs765506816 | in-del | -/TTT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444046 | GTGTTTTTTTTTTGT[-/TTT]TTTTTTTTTTTTTTT | 10054 |
rs765510684 | snp | A/G | 6.19444e-05 | 0.00556492 | missense, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428472 | CGGGAGCTGGCTGAG[A/G]CGGTGGCCGGGGGCC | 10054 |
rs765512665 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447760 | TTGCAGCCCTTGAAT[A/G]ATAAGTTTCATCTAA | 10054 |
rs765518394 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461781 | GAAGAAGGGAGATTG[-/T]TCAACAGCTGGATTG | 10054 |
rs765527310 | snp | A/C | 1.67643e-05 | 0.00289515 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469088 | CAGATGAAGAAGATT[A/C]TTCAAATAATGCCGA | 10054 |
rs765609004 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434670 | GGAGTAAATTTGTGA[C/T]ATAAATTCTATTTGA | 10054 |
rs765737655 | snp | A/C | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431913 | CTAATATCGTTGCCT[A/C]CCATGACAGCATCAT | 10054 |
rs765772822 | in-del | -/AA | 0.000401924 | 0.0141704 | intron-variant | UBA2 | GRCh38.p7 | 19:34460582 | TATCATACATTGTAT[-/AA]TTATTCATTCCTCTC | 10054 |
rs765778873 | snp | A/G | 1.93909e-05 | 0.00311369 | missense, intron-variant | UBA2 | GRCh38.p7 | 19:34460541 | AGGAACAATCCTAAT[A/G]TCTTCCGAAGAGGGA | 10054 |
rs765859148 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34463656 | GCCTAGCAGGCTGGA[A/G]TGCAGTGGTACAGTC | 10054 |
rs765919030 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429533 | AAGTTTCCTTTCACA[G/T]TTCTCAGGTTAATAG | 10054 |
rs765924922 | snp | A/G | 1.69968e-05 | 0.00291515 | intron-variant | UBA2 | GRCh38.p7 | 19:34464144 | TAGGTAAGAGCTATT[A/G]GTATTTTAATTGTAA | 10054 |
rs766043321 | in-del | -/ATATATATATATATAT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457180 | CTAAAAAAAAAAAAA[-/ATATATATATATATAT]ATATATATATATATA | 10054 |
rs766081956 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429150 | CAATGGGGTTGAGTA[A/G]CTTACCCTGGGTCAC | 10054 |
rs766083996 | snp | C/T | 3.34588e-05 | 0.00409002 | intron-variant | UBA2 | GRCh38.p7 | 19:34454246 | ACTTGTTAAATTGTT[C/T]AAATTATTGGCAGGA | 10054 |
rs766137009 | in-del | -/TG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455616 | TTGCAATGGTACTGT[-/TG]TATTTTGCAGTGTCA | 10054 |
rs766139489 | snp | G/T | 1.69132e-05 | 0.00290797 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469157 | ATGAGAAAGAGAATC[G/T]CAGTGCAAAGAGGTC | 10054 |
rs766152875 | snp | A/G | 1.64999e-05 | 0.00287222 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466892 | GTGAAGACCTAGGAA[A/G]GGACGTTGAATTTGA | 10054 |
rs766191418 | in-del | -/CTTTGG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458309 | CCTGTAATCCCAGCA[-/CTTTGG]CTTTGGGAGGCCGAG | 10054 |
rs766202420 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434414 | AGCCAGTGCTCCTGG[C/T]GTGAAATTACTCTCT | 10054 |
rs766212331 | in-del | -/TTTCG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461815 | TCGTCCAAGGAAAAC[-/TTTCG]TAGAAAGAGTGTGTA | 10054 |
rs766265280 | snp | C/T | 4.51681e-05 | 0.00475206 | intron-variant | UBA2 | GRCh38.p7 | 19:34435005 | TTAACTTCCCAAATA[C/T]TTATTTGAGACCTTG | 10054 |
rs766294084 | snp | G/T | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467740 | CCATCCAGCCTGGGT[G/T]ACAGAGCGAGGCTTC | 10054 |
rs766304367 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468665 | GAGTTGTCATATGCA[A/C]AGTGCTCAGAACAGT | 10054 |
rs766351030 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432658 | CGCCTCCTGGGTTCA[A/G]GCGATTCTCCTGTCT | 10054 |
rs766354987 | snp | A/G | 1.67643e-05 | 0.00289515 | intron-variant | UBA2 | GRCh38.p7 | 19:34454417 | TTTAAACAGTGAAAC[A/G]TACTCATCCTTTTTT | 10054 |
rs766421264 | snp | C/G | 0.000181191 | 0.00951644 | missense, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458832 | TGTGCACTGGATCCT[C/G]CCAACCCCAATTGTT | 10054 |
rs766436639 | in-del | -/T | 1.65187e-05 | 0.00287386 | frameshift-variant, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458769 | TTTCTCCTCCAAAGA[-/T]TTTTTTTGAATAAAC | 10054 |
rs766523011 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446436 | CCATTCTTCAGACAG[G/T]ATTTTCGTCTCTGTC | 10054 |
rs766748431 | snp | G/T | | | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426186 | TGTTTGTATGTACCT[G/T]ATTTTAACTCACAAG | 10054 |
rs766751351 | snp | C/T | 1.65081e-05 | 0.00287293 | intron-variant | UBA2 | GRCh38.p7 | 19:34430681 | ATATTTCTCATACCA[C/T]TTCTATAACTTGATG | 10054 |
rs766799955 | snp | A/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431908 | GAAAGCTAATATCGT[A/T]GCCTACCATGACAGC | 10054 |
rs766874191 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451049 | CCAGATTAGAGTGCA[A/G]TGGCTGTTCACAGGC | 10054 |
rs766891906 | snp | A/G | 2.14714e-05 | 0.00327647 | intron-variant | UBA2 | GRCh38.p7 | 19:34450415 | TGGAAATATCCTCGC[A/G]TAAAGTCTTTGTATA | 10054 |
rs766893670 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466210 | GTGTGGTGGCGCGCC[G/T]ATAGTCCCAGCTGCT | 10054 |
rs766926419 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438563 | GTAGTTGGAATATAG[A/G]TGAATGAAGTGTTTA | 10054 |
rs767004030 | snp | C/T | 1.67231e-05 | 0.00289159 | intron-variant | UBA2 | GRCh38.p7 | 19:34433458 | AGTATTTCCTCTCTC[C/T]CATATCAAATTTGTT | 10054 |
rs767050748 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34428997 | GGGCGGAGGATGGCA[A/G]TGATAGCGACCAACG | 10054 |
rs767058977 | snp | A/G | 1.6821e-05 | 0.00290004 | intron-variant | UBA2 | GRCh38.p7 | 19:34454225 | AAATAGTCAATTTGT[A/G]GAGAAACTTGTTAAA | 10054 |
rs767098230 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441732 | TTGAGAACTGCCTGG[A/G]CAACATGGCGAAACC | 10054 |
rs767228740 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453488 | TGAAAAAGAGTCATC[C/T]AGGTTTTTCTGAAGT | 10054 |
rs767292449 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440130 | GGAGTTTGAGAACAG[C/T]CTGGCCAACATGGCG | 10054 |
rs767363598 | in-del | -/C | 0.000175535 | 0.00936678 | intron-variant | UBA2 | GRCh38.p7 | 19:34454586 | TGCATTTTTATGCAA[-/C]CCCCCCTTAAAAAAA | 10054 |
rs767365980 | in-del | -/TTATT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431665 | GGGGGGGCTCTCCGG[-/TTATT]TTATAAGTATAAAAG | 10054 |
rs767387516 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466309 | CTACTGCACTCTAGC[C/T]TGGGTGACAGAGTGA | 10054 |
rs767396864 | snp | C/T | 1.93198e-05 | 0.00310797 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428455 | TGTCGCGGGGGCTGC[C/T]CCGGGAGCTGGCTGA | 10054 |
rs767397375 | snp | A/G | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467595 | ACCTGGGCAACACAG[A/G]GAAATCCCATCTGTA | 10054 |
rs767450764 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459768 | GAGGAGGAAGTGGCC[C/T]TTCTCAAATAGCAGT | 10054 |
rs767467878 | snp | A/C | 4.95258e-05 | 0.00497599 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452136 | GATGGAGCTGAGCTC[A/C]TATGGGATAAGGTTC | 10054 |
rs767500781 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432834 | TGCAGGGATTACAGG[C/T]GTGAGCCACTGCACC | 10054 |
rs767513822 | snp | C/T | 1.68917e-05 | 0.00290613 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469126 | GAAGAAGAGAGAAGC[C/T]GCAAGAGGAAATTAG | 10054 |
rs767587293 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444453 | ATAGAGCTGCGAGTT[C/G]TTCCTAGATCTCATG | 10054 |
rs767634002 | snp | G/T | 1.81082e-05 | 0.00300895 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34454493 | TACTAATGCAGTAAT[G/T]GCTGGGTTGATAGTA | 10054 |
rs767700828 | in-del | -/TTG | 1.6895e-05 | 0.00290641 | intron-variant | UBA2 | GRCh38.p7 | 19:34445159 | TCATGGATAGATGTA[-/TTG]TTGTGCATAGATGTA | 10054 |
rs767787976 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458250 | AGCTAGCCTAGCCTT[C/T]AGCTGATTAGAAAAG | 10054 |
rs767868336 | snp | C/T | 1.64923e-05 | 0.00287156 | intron-variant | UBA2 | GRCh38.p7 | 19:34430669 | GCACAGGTAACTATA[C/T]TTCTCATACCATTTC | 10054 |
rs767871747 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458792 | GAATAAACAACCAAA[C/T]CCAAGAAAGAAGCTT | 10054 |
rs767916845 | snp | A/G | 4.94776e-05 | 0.00497357 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450309 | GACAATGGACAAACT[A/G]TGGCGGAAAAGGAAA | 10054 |
rs768009995 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448087 | AGTGGGAATCCATTG[A/T]AAGGTGGTCTTACAG | 10054 |
rs768041032 | snp | A/G | 1.6651e-05 | 0.00288535 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464121 | ACTTTATTGATCAAC[A/G]TCCTTCATAGGTAAG | 10054 |
rs768061932 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34464514 | AGTCAGCCGGGATCG[C/T]GCCATTGCACTCCAA | 10054 |
rs768097853 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435120 | TTAAAATGCGGGGCC[A/G]GGTGCAGTGGCTCAT | 10054 |
rs768146952 | in-del | -/TAATGT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454955 | TTGTATAGTTTTTGA[-/TAATGT]TAATGTCTGAGATCT | 10054 |
rs768233493 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468402 | AAAATCATAATTTGA[A/C]ATGTACATTTATTGA | 10054 |
rs768247693 | snp | C/T | 2.56723e-05 | 0.00358266 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428549 | GAATCTCGTGCTCAC[C/T]GGTTTCTCCCACATC | 10054 |
rs768261217 | snp | C/G | 1.65745e-05 | 0.00287871 | intron-variant | UBA2 | GRCh38.p7 | 19:34454368 | TGTAAGTTATTTGTA[C/G]TAAAGTTGTATCACT | 10054 |
rs768266471 | in-del | -/TA | 1.65748e-05 | 0.00287874 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467019 | ACCTCCACAGGTGAG[-/TA]TATGGCCCCAGCCAG | 10054 |
rs768277632 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446154 | TAAGTGCTGGGATTA[C/T]AGGCATGAACCACTG | 10054 |
rs768299806 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461124 | CCTTCAGACTGTACT[C/T]GTTGATCCTATACCT | 10054 |
rs768311320 | snp | C/G | 1.66073e-05 | 0.00288156 | intron-variant | UBA2 | GRCh38.p7 | 19:34433442 | ATACTTTTAATTTCT[C/G]AGTATTTCCTCTCTC | 10054 |
rs768365473 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433955 | AGAGTGCGACCCTGT[C/G]TCAAAAAAAGAAAAA | 10054 |
rs768427671 | snp | A/G | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467335 | AAATTAACCACGCAT[A/G]GTAGCGTGTACCTGT | 10054 |
rs768487382 | snp | A/G | 4.0734e-05 | 0.0045128 | synonymous-codon, intron-variant | UBA2 | GRCh38.p7 | 19:34460553 | AATATCTTCCGAAGA[A/G]GGAGAGACGGAAGGT | 10054 |
rs768602405 | snp | A/G | 1.65078e-05 | 0.00287291 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466976 | CCAAAAGCATAACCA[A/G]TGGCAGTGATGATGG | 10054 |
rs768656738 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459500 | ATGACCTGATTCTGA[G/T]ATGGTAAGTTAGTCC | 10054 |
rs768662287 | snp | C/T | 1.97108e-05 | 0.00313927 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428439 | TGTCCCGCCATGGCA[C/T]TGTCGCGGGGGCTGC | 10054 |
rs768668419 | snp | A/G | 1.65839e-05 | 0.00287953 | intron-variant | UBA2 | GRCh38.p7 | 19:34450226 | TATCTTATCAATTAG[A/G]GATTATGGGGTTCAT | 10054 |
rs768719077 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442303 | GGGAAACCTAAATAA[A/G]CAATAAGCAAGTTAT | 10054 |
rs768723380 | snp | C/G | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445017 | GAACCAACGGAAGCC[C/G]AAGCCAGAGCTAGAG | 10054 |
rs768724353 | in-del | -/TTT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445436 | GCTTCTCATCTTCAC[-/TTT]TTTTTTTTTTTTTTT | 10054 |
rs768818315 | snp | A/G | 1.65312e-05 | 0.00287495 | intron-variant | UBA2 | GRCh38.p7 | 19:34466861 | TCATAGCAGTGACCT[A/G]TGTGATTCTCCTACA | 10054 |
rs768821964 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431878 | TGCCAAGGAAAGTGT[A/G]CTGCAGTTTTACCCG | 10054 |
rs768873340 | snp | A/G | 0.000164883 | 0.00907824 | intron-variant | UBA2 | GRCh38.p7 | 19:34430560 | TGTCATTTATCTGGG[A/G]TTTATGCATTTGTAG | 10054 |
rs768988117 | snp | A/C | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427692 | CAGGCGCACGCCACC[A/C]CGCCCGGCTAATTTT | 10054 |
rs769000544 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433327 | GTTATTTTGGTGACC[-/T]TTTTTTATTTTGTTT | 10054 |
rs769019163 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457519 | CCTTCCCGGTGAAGC[C/T]CAAAATCAAACAAAT | 10054 |
rs769109402 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429484 | CAAAAATTAGATAAA[A/C]CTTAAAACATGATAC | 10054 |
rs769131669 | in-del | -/ATAAA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440968 | TGGATCTAGAATCAT[-/ATAAA]ATAAAAAGTGTGTCT | 10054 |
rs769213360 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433784 | AGTCAACATGGTGAA[A/G]CCGTCTCTACCAAAA | 10054 |
rs769284607 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432652 | AACCTCCGCCTCCTG[A/G]GTTCAAGCGATTCTC | 10054 |
rs769365009 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454427 | GAAACATACTCATCC[-/T]TTTTTTTTTTTCCCA | 10054 |
rs769366116 | in-del | -/TT/TTT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431234 | TTACTTTTCCTATCA[-/TT/TTT]TTTTCTTTTCTTTTT | 10054 |
rs769406674 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459414 | ACAGTGCCCACTCCC[A/G]GCAAATTAGGGGGCT | 10054 |
rs769560340 | snp | C/T | 2.01221e-05 | 0.00317186 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428427 | GCGGCTCGTGGTTGT[C/T]CCGCCATGGCACTGT | 10054 |
rs769670689 | in-del | -/AAAAAAA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458559 | GCAAGACTCCGTCTC[-/AAAAAAA]AAAAAAAAAAAAAAA | 10054 |
rs769725472 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448904 | AGATGGAGCTTAGGC[C/T]TAGAAAACTGTTGGT | 10054 |
rs769745981 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449026 | ACATGTTGCTGTCAT[A/G]AGGAGACTCTTTCCT | 10054 |
rs769834912 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436922 | AAGTGGAGGCCTTCA[A/G]TATCTGTTGACAGAT | 10054 |
rs769858860 | snp | A/G | 1.65864e-05 | 0.00287974 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464068 | TTGGAATTAGAAATG[A/G]CAGCCGGCTTCAAGC | 10054 |
rs769863413 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458917 | CTGTTCTCACCTTAC[A/G]AGACAAGGTCAGTGC | 10054 |
rs769920585 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438016 | AGATTATGCCACTGT[A/T]CTCCAGCCAGGGTGA | 10054 |
rs769921817 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34464372 | AGACCAACCTGGCCA[A/G]CACGGTGAAACCCCG | 10054 |
rs769946567 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451838 | GGCGTGAGCCACCGT[G/T]CCTGGCCCCATGATA | 10054 |
rs769950788 | snp | A/G | | | intron-variant, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34430123 | TATTTTGCTTAGGCT[A/G]GTCTTGAAGGTCTGG | 10054 |
rs769962528 | snp | G/T | 1.84544e-05 | 0.00303758 | intron-variant | UBA2 | GRCh38.p7 | 19:34450388 | TACATTTTAGTCTTG[G/T]AACACCTAAGCTGGA | 10054 |
rs770015909 | snp | C/T | 1.65121e-05 | 0.00287329 | intron-variant | UBA2 | GRCh38.p7 | 19:34450259 | GATCTGTCTTTCTTT[C/T]GTAAGCTTTTTAAAG | 10054 |
rs770052012 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462742 | GGGCCGAGGCGGGCA[C/G]ATCACTTGAGGCCAG | 10054 |
rs770090531 | snp | A/G | 6.73219e-05 | 0.00580142 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469105 | TCAAATAATGCCGAC[A/G]TCAGTGAAGAAGAGA | 10054 |
rs770129751 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442442 | AGTAAAAAATGATGC[C/T]TTTTTTGTTGTTGTT | 10054 |
rs770219365 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429165 | ACTTACCCTGGGTCA[A/C]GGAGCGAGTGGCAGG | 10054 |
rs770234024 | snp | G/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452106 | ACTTTGAGAGTTCAT[G/T]TAGCAGAAAAGGGGG | 10054 |
rs770373263 | snp | G/T | 6.34296e-05 | 0.00563123 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34434938 | AAGTGGAACAGCTGG[G/T]TATCTTGGACAAGTA | 10054 |
rs770454400 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455903 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 10054 |
rs770460593 | snp | C/G | 1.64768e-05 | 0.00287021 | synonymous-codon, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458900 | GAATGTCCATAAAGT[C/G]ACTGTTCTCACCTTA | 10054 |
rs770584191 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34430701 | ATAACTTGATGGAGC[C/T]TCTATTTGTGATACC | 10054 |
rs770620132 | snp | C/G | 4.94482e-05 | 0.00497209 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34443872 | GAAGAAGATGCTGAT[C/G]AAGAAGTATCTCCTG | 10054 |
rs770675299 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457747 | TAGTCACAAGATAAA[G/T]GTTTGTGTCTCAGCT | 10054 |
rs770743309 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434825 | ATTAAAGATAACTAA[-/T]TTTTTTTTTCCCAAA | 10054 |
rs770787276 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460821 | CCGATATCATGGATC[C/T]TGGGAGCTAACCTTG | 10054 |
rs770863390 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462421 | TTGAATGTGATGGTT[C/T]CAAGAGGTTTGCAGT | 10054 |
rs770893479 | snp | G/T | 3.30786e-05 | 0.00406672 | intron-variant | UBA2 | GRCh38.p7 | 19:34433418 | GATAACAGAGGTGAG[G/T]TTATTTTAATACTTT | 10054 |
rs770965639 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435518 | GAGTGGTAAGCATGA[G/T]ATACCAGGCATCAAA | 10054 |
rs771020313 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445040 | AGCTAGAGCATCTAA[C/T]GAAGATGGTGACATT | 10054 |
rs771094791 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462578 | TTTCTGGGTGTCAAC[A/G]TAGGGAAAGGCGTTC | 10054 |
rs771123853 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441149 | ATGATGAAAGTTTCT[A/G]CTAAAACAGAATAAA | 10054 |
rs771145691 | snp | A/G | 1.65809e-05 | 0.00287926 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464038 | TAGCTAATAATCACA[A/G]GAAGTTGTCAGAATT | 10054 |
rs771411735 | snp | A/C | 7.43674e-05 | 0.00609739 | intron-variant | UBA2 | GRCh38.p7 | 19:34469035 | TCCCTTTTTTCTGAA[A/C]TAAGCTCAAGAGCAA | 10054 |
rs771419613 | snp | A/C/T | 0.000309562 | 0.012438 | intron-variant | UBA2 | GRCh38.p7 | 19:34431973 | GTTGTATAAGGGTTT[A/C/T]GTAAGCCAAATATAT | 10054 |
rs771463029 | snp | C/T | 3.32011e-05 | 0.00407424 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467027 | CAGGTGAGTATGGCC[C/T]CAGCCAGCAGGTTGT | 10054 |
rs771522402 | snp | C/T | 1.66507e-05 | 0.00288532 | intron-variant | UBA2 | GRCh38.p7 | 19:34452176 | ATGTGTGGCAAGTAC[C/T]TACATGTCAAAAGTG | 10054 |
rs771561345 | snp | C/G | 1.66098e-05 | 0.00288177 | intron-variant | UBA2 | GRCh38.p7 | 19:34454380 | GTACTAAAGTTGTAT[C/G]ACTAAAACCTTGAAG | 10054 |
rs771579414 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468167 | GGAAACTAAAGGTTA[C/T]CAGATTTTGACTTCT | 10054 |
rs771608712 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458106 | GAATAGCCTCAGGGA[A/G]GGACACCAGCTGCTG | 10054 |
rs771623364 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468448 | AGGTTTCCAAGGTTA[C/T]AGCCATGAGTAAGAT | 10054 |
rs771665690 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34438675 | TATGAGTGTCATCCT[A/G]AGCCGACCCAGAGAA | 10054 |
rs771715015 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435225 | AAGCATGGTGAAACC[C/G]CATCTCTACTAAAAA | 10054 |
rs771716935 | snp | C/T | 1.68428e-05 | 0.00290192 | intron-variant | UBA2 | GRCh38.p7 | 19:34458718 | TTAGATTGTATGGCG[C/T]ATAAAATTACAGCAC | 10054 |
rs771719036 | snp | A/C | 7.49372e-05 | 0.0061207 | intron-variant | UBA2 | GRCh38.p7 | 19:34434994 | GTTTTATTTTTTTAA[A/C]TTCCCAAATATTTAT | 10054 |
rs771773152 | snp | A/G | | | downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34469983 | AACTCGGTCGGGCAC[A/G]GTGGCTCATGCCTGT | 10054 |
rs771784590 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435348 | GGTTGCAGTAAGCTG[A/C]GATTGCACCACTGCC | 10054 |
rs771794453 | in-del | -/T | 1.98916e-05 | 0.00315363 | intron-variant | UBA2 | GRCh38.p7 | 19:34469023 | CATTTTCTTTTTCCC[-/T]TTTTTTCTGAAATAA | 10054 |
rs771826563 | in-del | -/CTTAG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440506 | TAAAAGGGAATACTA[-/CTTAG]CTTGTGTTATTAGGC | 10054 |
rs771832556 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434166 | GTTGCCCAGACTAGA[A/G]TGCACTGGTGTGATC | 10054 |
rs771879232 | snp | C/G | 1.65405e-05 | 0.00287576 | intron-variant | UBA2 | GRCh38.p7 | 19:34450247 | TGGGGTTCATGGGAT[C/G]TGTCTTTCTTTTGTA | 10054 |
rs772024003 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452055 | CAGGTTCTAGATGTA[A/G]AGAGCTATGCACGTC | 10054 |
rs772038466 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466178 | TCTCTACTAAAAATA[-/G]CAAAAAAATTAGCCA | 10054 |
rs772078393 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440850 | AGAATTGCTTGAACC[C/T]GGGAGGTGGAGGCTG | 10054 |
rs772086332 | snp | A/G | 0.00087146 | 0.0208559 | intron-variant, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34430100 | TCTTGTAGCCACCAG[A/G]GTCTCACTATTTTGC | 10054 |
rs772104168 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34446342 | CCACATAACCGAAAA[C/T]TCTTTTTCTTTCTGC | 10054 |
rs772167417 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431893 | ACTGCAGTTTTACCC[A/G]AAAGCTAATATCGTT | 10054 |
rs772188953 | snp | A/C | 0.000165599 | 0.0090979 | intron-variant | UBA2 | GRCh38.p7 | 19:34438812 | CGGTACTGATGATGG[A/C]AAATGGAGTCATTTT | 10054 |
rs772190461 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462258 | ACTAAGGCAGAGGCA[A/G]GTGATAGATTTGAGA | 10054 |
rs772202584 | snp | C/G | 2.4773e-05 | 0.00351936 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428561 | CACCGGTTTCTCCCA[C/G]ATCGACCTGGTGAGG | 10054 |
rs772222492 | snp | C/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427319 | GTGCTTGTTTCCCAA[C/T]CCCTTGATAAGTGTT | 10054 |
rs772248573 | snp | A/G | 1.64953e-05 | 0.00287182 | intron-variant | UBA2 | GRCh38.p7 | 19:34431950 | TGCTATAGTGATTAC[A/G]TTGCAAAGTTGTATA | 10054 |
rs772296248 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442557 | CCTGCTCAGCCTCTC[A/G]AGTGGCTGGGATTAC | 10054 |
rs772322922 | in-del | -/GAAAATATGAAA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450454 | TTGCTTGAAAATGAT[-/GAAAATATGAAA]ATGTCTTCATATATT | 10054 |
rs772346422 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439693 | AAATGAGCCAGGTGT[A/G]CCTGTACTCCCAGCT | 10054 |
rs772384824 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450669 | GTATAGTTAACTAGT[C/T]TCTTATTAACATGTA | 10054 |
rs772439326 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466840 | GCTCCTTTGCTTTCT[A/G]AATAGTCATAGCAGT | 10054 |
rs772540234 | snp | A/C | 1.68388e-05 | 0.00290158 | intron-variant | UBA2 | GRCh38.p7 | 19:34458721 | GATTGTATGGCGTAT[A/C]AAATTACAGCACGTT | 10054 |
rs772614183 | in-del | -/TT | 0.0450258 | 0.143128 | intron-variant | UBA2 | GRCh38.p7 | 19:34451967 | TTTCTAATATATATA[-/TT]TTTTTTTCTTTAGGA | 10054 |
rs772659086 | snp | A/T | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427892 | TTTTTTGAGACGGAG[A/T]CTTGCTCTGTTACCC | 10054 |
rs772710417 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454163 | TCTAGTCGAAAGTCT[A/G]TAGTATTATAAACAC | 10054 |
rs772722686 | snp | C/T | 1.654e-05 | 0.00287571 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34467004 | TGGAGCTCAGCCCTC[C/T]ACCTCCACAGGTGAG | 10054 |
rs772742814 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432340 | ACTTGGAATTGTGGT[A/C]GGGCAGTAGTATTGA | 10054 |
rs772758782 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455862 | GGTTAGGCTGGTCTC[A/G]AACTCCTGACCTCAT | 10054 |
rs772776689 | snp | A/G | 1.66269e-05 | 0.00288326 | intron-variant | UBA2 | GRCh38.p7 | 19:34454393 | ATCACTAAAACCTTG[A/G]AGTTGTTTTTTAAAC | 10054 |
rs772815901 | snp | C/G/T | 4.87582e-05 | 0.00493732 | intron-variant | UBA2 | GRCh38.p7 | 19:34428580 | GACCTGGTGAGGGCC[C/G/T]GGCGCGCGCGCGTGA | 10054 |
rs772883163 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34438680 | GTGTCATCCTAAGCC[A/G]ACCCAGAGAACCTTT | 10054 |
rs772887831 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442631 | ATACAGGGTTTCACC[C/T]TGTTGGCCAGGCTGG | 10054 |
rs772938339 | snp | C/T | 1.65375e-05 | 0.0028755 | intron-variant | UBA2 | GRCh38.p7 | 19:34450248 | GGGGTTCATGGGATC[C/T]GTCTTTCTTTTGTAA | 10054 |
rs773023245 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441754 | GGCGAAACCCTGTCT[C/G]TACTAAAAATACAAA | 10054 |
rs773052570 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434351 | GAACTCCTGGCTTCA[A/T]GCAGTCCTCCCACCT | 10054 |
rs773106408 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435364 | GATTGCACCACTGCC[C/T]TCCAGCCTGGGCTAC | 10054 |
rs773116538 | snp | A/C | 0.000330387 | 0.0128485 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428457 | TCGCGGGGGCTGCCC[A/C]GGGAGCTGGCTGAGG | 10054 |
rs773122522 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439208 | TGAGAATTTGTCTCA[-/A]AAAAAAAAAAAAAAA | 10054 |
rs773178552 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451537 | TCTCAGGTTTAACAG[-/T]TTTTTTTTTTTTTTT | 10054 |
rs773274889 | snp | A/G | 7.7994e-05 | 0.00624427 | intron-variant | UBA2 | GRCh38.p7 | 19:34431958 | TGATTACATTGCAAA[A/G]TTGTATAAGGGTTTT | 10054 |
rs773284354 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466179 | TCTCTACTAAAAATA[A/C]AAAAAAATTAGCCAG | 10054 |
rs773464341 | snp | A/G | 0.000217212 | 0.0104191 | intron-variant | UBA2 | GRCh38.p7 | 19:34458968 | TTTTGCTTTTACAGT[A/G]TTACTGTGATGACAA | 10054 |
rs773489948 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461622 | TTCAGCGTGACCCTT[C/T]TGTACGGAATACATG | 10054 |
rs773564267 | snp | A/C | 1.72761e-05 | 0.002939 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34451989 | TCTTTAGGAGAAGAA[A/C]CGAATGCATCAGATC | 10054 |
rs773581952 | in-del | -/AGA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458183 | GCCAAATCAGGTTGC[-/AGA]AGAACGCGGAGTCTT | 10054 |
rs773605844 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438518 | TTTTGGAGTCACTAA[A/T]ATTTTAAAATTTCCT | 10054 |
rs773606106 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34452611 | TTATTCTTAGAAGTT[A/G]AAATCATATTTAATA | 10054 |
rs773613168 | snp | C/G/T | 4.96071e-05 | 0.00498011 | intron-variant | UBA2 | GRCh38.p7 | 19:34466859 | AGTCATAGCAGTGAC[C/G/T]TGTGTGATTCTCCTA | 10054 |
rs773720762 | snp | G/T | 1.65037e-05 | 0.00287256 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466882 | TTCTCCTACAGTGAA[G/T]ACCTAGGAAAGGACG | 10054 |
rs773760841 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432482 | TTGCAAGTAAATAGT[A/G]TTAAAAATAGTCCTT | 10054 |
rs773800034 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457517 | TACCTTCCCGGTGAA[A/G]CCCAAAATCAAACAA | 10054 |
rs773804523 | snp | G/T | 1.68275e-05 | 0.0029006 | intron-variant | UBA2 | GRCh38.p7 | 19:34454216 | AATGCTTCAAAATAG[G/T]CAATTTGTGGAGAAA | 10054 |
rs773848330 | snp | A/G | 1.66076e-05 | 0.00288158 | intron-variant | UBA2 | GRCh38.p7 | 19:34433443 | TACTTTTAATTTCTC[A/G]GTATTTCCTCTCTCC | 10054 |
rs773851430 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455012 | TTTCTGCTATTTCTC[A/G]TAGTGATTTGCTTGT | 10054 |
rs773857522 | snp | C/G | 1.68664e-05 | 0.00290395 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469117 | GACGTCAGTGAAGAA[C/G]AGAGAAGCCGCAAGA | 10054 |
rs773976671 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453405 | AAAACTTGGATTGTA[C/T]TGCCTTATTTGAAGA | 10054 |
rs773980206 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34434007 | GGGGATGCTTGAGTG[A/T]TATTCTTTGTCTGTA | 10054 |
rs773980353 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34468407 | CATAATTTGAAATGT[A/G]CATTTATTGATTCTC | 10054 |
rs774051623 | snp | A/C | 2.50241e-05 | 0.00353715 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428557 | TGCTCACCGGTTTCT[A/C]CCACATCGACCTGGT | 10054 |
rs774083532 | snp | A/G | 4.16017e-05 | 0.0045606 | synonymous-codon, intron-variant | UBA2 | GRCh38.p7 | 19:34460556 | ATCTTCCGAAGAGGG[A/G]GAGACGGAAGGTATC | 10054 |
rs774108887 | snp | C/T | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467340 | AACCACGCATGGTAG[C/T]GTGTACCTGTAGTCT | 10054 |
rs774131542 | in-del | -/AGA | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439894 | ATTTGATTACAAAAT[-/AGA]AGAGGAGTAAGTGAG | 10054 |
rs774148442 | in-del | -/A | 4.2603e-05 | 0.00461516 | intron-variant | UBA2 | GRCh38.p7 | 19:34469001 | AGGTAACTCCCACGC[-/A]TTTTACCCATTTTCT | 10054 |
rs774173636 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432766 | CATCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC | 10054 |
rs774232159 | snp | C/T | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445022 | AACGGAAGCCGAAGC[C/T]AGAGCTAGAGCATCT | 10054 |
rs774257506 | snp | A/G | 1.72835e-05 | 0.00293964 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469063 | CAAGATGACGTTCTC[A/G]TAGTTGATTCAGATG | 10054 |
rs774357307 | snp | C/T | 2.00761e-05 | 0.00316822 | intron-variant | UBA2 | GRCh38.p7 | 19:34450408 | CCTAAGCTGGAAATA[C/T]CCTCGCGTAAAGTCT | 10054 |
rs774358685 | snp | A/G | 1.65037e-05 | 0.00287256 | intron-variant | UBA2 | GRCh38.p7 | 19:34443930 | AGTAAATTATTTGGC[A/G]TATGTTTTATCAGAT | 10054 |
rs774395120 | in-del | -/A | 7.09019e-05 | 0.00595365 | intron-variant | UBA2 | GRCh38.p7 | 19:34454581 | TCTGTTTGCATTTTT[-/A]TGCAACCCCCCTTAA | 10054 |
rs774412201 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465936 | GACTTAAATGTTTCT[G/T]ATGTTTTTGGGAGTT | 10054 |
rs774435691 | snp | A/T | 3.75382e-05 | 0.00433217 | splice-acceptor-variant | UBA2 | GRCh38.p7 | 19:34451979 | TATATTTTTTTCTTT[A/T]GGAGAAGAAACGAAT | 10054 |
rs774460249 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450140 | TGAAAATTGTTATGC[-/T]GCTGGTATATGACAT | 10054 |
rs774496297 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34450604 | ATTCGTTATACACTG[C/T]GTAAATGGAATCATA | 10054 |
rs774510935 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431679 | GTTATTTTATAAGTA[-/T]AAAAGTATAATTTTA | 10054 |
rs774583903 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431890 | TGTACTGCAGTTTTA[C/T]CCGAAAGCTAATATC | 10054 |
rs774595373 | in-del | -/A | 1.65663e-05 | 0.002878 | intron-variant | UBA2 | GRCh38.p7 | 19:34433425 | AGGTGAGGTTATTTT[-/A]AATACTTTTAATTTC | 10054 |
rs774664167 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438365 | CAAGGTAAACTCATA[C/T]TTGACACTCAGGTGT | 10054 |
rs774678151 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34464481 | GAGAATCCCTTGAAC[C/T]CGAGAGGTGGAGGTT | 10054 |
rs774695616 | snp | C/T | 9.91146e-05 | 0.007039 | intron-variant | UBA2 | GRCh38.p7 | 19:34466871 | GACCTGTGTGATTCT[C/T]CTACAGTGAAGACCT | 10054 |
rs774733807 | snp | A/G | 1.65982e-05 | 0.00288077 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464086 | GCCGGCTTCAAGCAG[A/G]TGACTTCCTCCAGGA | 10054 |
rs774799787 | snp | A/C | 0.00020536 | 0.010131 | utr-variant-5-prime, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428429 | GGCTCGTGGTTGTCC[A/C]GCCATGGCACTGTCG | 10054 |
rs774817880 | in-del | -/AT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34452487 | TGGAGAAAACATCTC[-/AT]TGGCCTGATTTGCCC | 10054 |
rs774818251 | snp | C/T | 1.74708e-05 | 0.00295552 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469056 | TCAAGAGCAAGATGA[C/T]GTTCTCATAGTTGAT | 10054 |
rs774840183 | snp | A/T | 6.93049e-05 | 0.00588622 | intron-variant | UBA2 | GRCh38.p7 | 19:34434990 | AAAAGTTTTATTTTT[A/T]TAACTTCCCAAATAT | 10054 |
rs774984418 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429485 | AAAAATTAGATAAAA[C/T]TTAAAACATGATACT | 10054 |
rs774986076 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34443681 | TCCTGACTTTGTGAT[C/T]TGCCTGCCTCAGCCT | 10054 |
rs775002456 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34430320 | CCTGAAATATTTTCC[A/G]GGATGATTAAACAAA | 10054 |
rs775039102 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432684 | TGTCTCAGCCTCCTG[A/G]GTAGTTGGGATTACA | 10054 |
rs775070397 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445285 | AGTCAGGATATGCAA[A/G]TTTTAAAATGTTACC | 10054 |
rs775115177 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466048 | TATAGTTAAGATCAC[A/G]TTGTAGGCCAGGCGT | 10054 |
rs775154655 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431356 | CTCCTGGCCTCAAGG[A/G]ATCCTCCTACACTGG | 10054 |
rs775179504 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34454807 | GAAGAATTCATTGTG[C/T]GGTCCTTATACTAAG | 10054 |
rs775330873 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459421 | CCACTCCCAGCAAAT[G/T]AGGGGGCTTTTGTTA | 10054 |
rs775334519 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444126 | ACAATGGTATAATCT[C/T]GGCTCACTGCAACCT | 10054 |
rs775373199 | snp | C/T | 4.94605e-05 | 0.0049727 | synonymous-codon, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458921 | TCTCACCTTACAAGA[C/T]AAGGTCAGTGCAAGG | 10054 |
rs775534336 | snp | C/T | 9.89169e-05 | 0.00703197 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34443911 | GACCCTGAAGCTGCC[C/T]GTGAGTAAATTATTT | 10054 |
rs775551383 | snp | C/G | 1.65891e-05 | 0.00287998 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464069 | TGGAATTAGAAATGG[C/G]AGCCGGCTTCAAGCA | 10054 |
rs775557006 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438018 | ATTATGCCACTGTAC[G/T]CCAGCCAGGGTGACA | 10054 |
rs775616765 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444542 | CAGGCAAGGTGGCTC[-/A]ACGCCCGTAGTCCCA | 10054 |
rs775715477 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34464393 | TGAAACCCCGTCTCT[A/G]CTAAAAATGCAAAAA | 10054 |
rs775752073 | snp | A/G | 2.44849e-05 | 0.00349884 | intron-variant | UBA2 | GRCh38.p7 | 19:34428582 | CCTGGTGAGGGCCGG[A/G]CGCGCGCGCGTGAAT | 10054 |
rs775755415 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436971 | TCTGCATTGCAGTAT[G/T]AGTCTCATGACTGCT | 10054 |
rs775894014 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442475 | TTTGAGATGGAGTTT[C/T]GCTCTTGTTGCCCAG | 10054 |
rs775937019 | snp | C/T | 0.00014923 | 0.00863671 | intron-variant | UBA2 | GRCh38.p7 | 19:34433434 | TTATTTTAATACTTT[C/T]AATTTCTCAGTATTT | 10054 |
rs775944623 | snp | A/T | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34443883 | TGATCAAGAAGTATC[A/T]CCTGACAGAGCTGAC | 10054 |
rs775960390 | snp | A/C | 2.51253e-05 | 0.00354429 | intron-variant | UBA2 | GRCh38.p7 | 19:34460588 | TACATTGTATTTATT[A/C]ATTCCTCTCATTGAG | 10054 |
rs775985439 | snp | C/G/T | 5.0173e-05 | 0.00500843 | intron-variant | UBA2 | GRCh38.p7 | 19:34452192 | TACATGTCAAAAGTG[C/G/T]GTTTTAGTTCTTGAG | 10054 |
rs776007825 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441572 | TCAGCAAACATTGTC[A/T]TTAATTTTTGCACTC | 10054 |
rs776066081 | snp | A/G | 1.65853e-05 | 0.00287964 | intron-variant | UBA2 | GRCh38.p7 | 19:34431982 | GGGTTTTGTAAGCCA[A/G]ATATATAAGCTCAAA | 10054 |
rs776091327 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465428 | TGGATCACGAGGTCA[-/G]GAGTTCAAGACCAGC | 10054 |
rs776126905 | snp | A/C | 1.66443e-05 | 0.00288477 | intron-variant, utr-variant-3-prime | UBA2 | GRCh38.p7 | 19:34467046 | CCAGCAGGTTGTTAA[A/C]TACCCACAAAGCAGA | 10054 |
rs776172916 | in-del | -/GGTGCT | | | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426241 | GCCTTTTTGCCTTTG[-/GGTGCT]GGTGCTGGTGCCGGG | 10054 |
rs776208385 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457869 | CAGTGTAATTTGTAT[A/T]TTTGCCTTGGTTCTT | 10054 |
rs776350927 | snp | C/T | 1.64939e-05 | 0.0028717 | intron-variant | UBA2 | GRCh38.p7 | 19:34430555 | ACGTTTGTCATTTAT[C/T]TGGGGTTTATGCATT | 10054 |
rs776410820 | in-del | -/AC | 3.3557e-05 | 0.00409602 | intron-variant | UBA2 | GRCh38.p7 | 19:34454238 | TGGAGAAACTTGTTA[-/AC]AATTGTTTAAATTAT | 10054 |
rs776440034 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34461273 | TGACTTAATTCATAC[C/T]TATTTGTCCATTGGT | 10054 |
rs776463970 | in-del | -/TTT | 8.84525e-05 | 0.00664969 | intron-variant | UBA2 | GRCh38.p7 | 19:34434825 | ATTAAAGATAACTAA[-/TTT]TTTTTTTCCCAAAAA | 10054 |
rs776606686 | snp | A/G | 8.39511e-05 | 0.00647831 | intron-variant | UBA2 | GRCh38.p7 | 19:34458734 | ATAAAATTACAGCAC[A/G]TTTCCGATTTCTGCC | 10054 |
rs776638349 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445218 | TAGTCCATAAAATTG[-/A]ATTAAGCTTCTATGT | 10054 |
rs776644251 | snp | C/T | 2.31613e-05 | 0.00340296 | intron-variant | UBA2 | GRCh38.p7 | 19:34460577 | GGAAGGTATCATACA[C/T]TGTATTTATTCATTC | 10054 |
rs776692432 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34435541 | GCATCAAAAATTTCT[G/T]TGTGTCGGCTGCGTG | 10054 |
rs776805745 | snp | C/T | 1.65825e-05 | 0.00287941 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34464060 | GTCAGAATTTGGAAT[C/T]AGAAATGGCAGCCGG | 10054 |
rs776824258 | snp | A/G | | | upstream-variant-2KB | UBA2 | GRCh38.p7 | 19:34427670 | GCCTCCCGAGTAGCT[A/G]GGATTACAGGCGCAC | 10054 |
rs776883509 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445053 | AATGAAGATGGTGAC[A/G]TTAAACGTATTTCTA | 10054 |
rs776887295 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34447511 | TCCATTCCAATCTGA[A/G]CAAGACTTGAAAGCC | 10054 |
rs776902990 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441375 | CAGGAGAATGGCGTG[A/G]ACCCGGGAGGCGGAG | 10054 |
rs776932517 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462608 | CTAAGCGTTTTCCTT[A/G]TAAATAATGAAAAAA | 10054 |
rs777025042 | snp | A/G | | | intron-variant, upstream-variant-2KB | PDCD2L, UBA2 | GRCh38.p7 | 19:34426201 | TATTTTAACTCACAA[A/G]TTATTAACCTCTGTT | 10054 |
rs777027812 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453929 | GGAAAGGGTTGCCAT[A/T]GTCAGTGAGTGGAAT | 10054 |
rs777055477 | snp | A/T | 1.81243e-05 | 0.00301029 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469041 | TTTTCTGAAATAAGC[A/T]CAAGAGCAAGATGAC | 10054 |
rs777077347 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34431909 | AAAGCTAATATCGTT[A/G]CCTACCATGACAGCA | 10054 |
rs777085650 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452088 | TTTTCAAAGAGCATC[A/G]AGACTTTGAGAGTTC | 10054 |
rs777136817 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453063 | GAGTAAAGTCCACAT[C/G]TAATGGGTGTGATAA | 10054 |
rs777203834 | snp | A/G | 1.69318e-05 | 0.00290957 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34451993 | TAGGAGAAGAAACGA[A/G]TGCATCAGATCAACA | 10054 |
rs777222906 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439920 | AAGTGAGAACTAAAC[A/G]GGGAATACAGATAGC | 10054 |
rs777283315 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436743 | AAAGAGAATTATAAT[A/G]TACTTAACATTTGCT | 10054 |
rs777323882 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34464876 | GCATTTTGGGAGGTC[A/G]AGGCGGGTGGATCAC | 10054 |
rs777379660 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457617 | TTGTACGGAGAAGCT[A/G]TTTTACAGAGGACGG | 10054 |
rs777474708 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448455 | AAAAAATAGCCAGCC[A/G]TGGTGGCCTGAGCCT | 10054 |
rs777491546 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437779 | ATAAAATGGGCTGGG[C/T]GCAGTGGCTCACGCC | 10054 |
rs777497418 | in-del | -/CCGCCT | | | utr-variant-5-prime, cds-indel, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428394 | CGCGGCTCGGTTCTC[-/CCGCCT]CCGCCTCCGCCTCCG | 10054 |
rs777514183 | snp | C/T | 3.29484e-05 | 0.00405871 | missense, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458880 | CCAGAGGTGACTGTG[C/T]GGCTGAATGTCCATA | 10054 |
rs777565481 | snp | C/T | 1.82837e-05 | 0.00302349 | intron-variant | UBA2 | GRCh38.p7 | 19:34450384 | AGAATACATTTTAGT[C/T]TTGGAACACCTAAGC | 10054 |
rs777609385 | snp | C/T | 1.65726e-05 | 0.00287855 | intron-variant | UBA2 | GRCh38.p7 | 19:34466834 | TCTGGTGCTCCTTTG[C/T]TTTCTAAATAGTCAT | 10054 |
rs777683786 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34444802 | ACAGAGTGAGACTTT[G/T]TCTCCAAAAACAAGA | 10054 |
rs777687061 | snp | C/G | | | upstream-variant-2KB, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428311 | CGCGATGTGCCCTGC[C/G]TGTGTCTGCCGGAGG | 10054 |
rs777778716 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442179 | GGTCGAGGCTGCAGT[G/T]AGCTGTGATCACACC | 10054 |
rs777790811 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462330 | TACAATGTTAGCAGC[A/G]TTGTTAGGCGAGCAC | 10054 |
rs777798268 | snp | C/T | 1.65247e-05 | 0.00287438 | intron-variant | UBA2 | GRCh38.p7 | 19:34430535 | TACAGCTCAAACATA[C/T]GTAAACGTTTGTCAT | 10054 |
rs777842929 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469381 | AGAACTGTTAGACAC[A/G]TTGCAGTATGCTGTA | 10054 |
rs777860871 | snp | C/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34455167 | ACTGCCAATACAGGA[C/G]CACTTTTAAATTAGG | 10054 |
rs777935548 | snp | C/T | 1.65979e-05 | 0.00288074 | intron-variant | UBA2 | GRCh38.p7 | 19:34452162 | GGTTCGTTTTGACAA[C/T]GTGTGGCAAGTACTT | 10054 |
rs777968951 | snp | A/G | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452068 | TAAAGAGCTATGCAC[A/G]TCTTTTTTCAAAGAG | 10054 |
rs777973567 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34440858 | TTGAACCCGGGAGGT[A/G]GAGGCTGCAGTGAGC | 10054 |
rs777999005 | snp | C/T | | | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34433348 | TATTTTGTTTTGTAG[C/T]CCTGACTATAATGTG | 10054 |
rs778045326 | snp | A/G | 1.67607e-05 | 0.00289483 | intron-variant | UBA2 | GRCh38.p7 | 19:34444958 | AAAGAGTTCAGTTCT[A/G]CATTTATTACGGTTG | 10054 |
rs778056215 | snp | C/T | 5.63269e-05 | 0.00530663 | missense, intron-variant | UBA2 | GRCh38.p7 | 19:34460474 | TTTTTTTGTAGATAG[C/T]GAAAGAAAAATTTGC | 10054 |
rs778131908 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445902 | AGAGAAATCTGTGAA[A/G]TTGTTTTTATTGGGT | 10054 |
rs778152932 | snp | A/T | 0.000244505 | 0.0110541 | intron-variant | UBA2 | GRCh38.p7 | 19:34434848 | TTCCCAAAAACTCAT[A/T]CTGTTTGTTTTACTT | 10054 |
rs778168210 | snp | G/T | 1.64923e-05 | 0.00287156 | intron-variant | UBA2 | GRCh38.p7 | 19:34443839 | TTACTATTCTTAAAT[G/T]ATAGCCAGTTGTTTG | 10054 |
rs778252250 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34430259 | ACCTCGACAGCACAT[-/A]ATAGTTTTAATGAAT | 10054 |
rs778276299 | snp | C/T | 0.00064704 | 0.017975 | utr-variant-5-prime, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428402 | CGGTTCTCCCGCCTC[C/T]GCCTCCGCCGCGGCT | 10054 |
rs778288448 | in-del | -/TT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460452 | TAATATTTTGAATCC[-/TT]TTTTTTTTTTTTGTA | 10054 |
rs778346245 | snp | C/T | 1.90116e-05 | 0.00308309 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469264 | TTACTATTTAGTTTA[C/T]CTGGGCAGAACCAGA | 10054 |
rs778384280 | in-del | -/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34466086 | ACACCTGTAATCCCA[-/G]GCACTTTGGGAGGCT | 10054 |
rs778448025 | in-del | -/CT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456104 | TTTTCCTTTTCTTTT[-/CT]TCTTTTTTTTTTTTT | 10054 |
rs778458035 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456303 | TATTATTAGTAGAGA[C/T]GGTGTTTCACCTGTT | 10054 |
rs778505251 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460132 | TATGAAACCCCTGCC[A/G]TTACAGGGTTGGCAC | 10054 |
rs778561963 | snp | A/G | 2.63564e-05 | 0.00363008 | intron-variant | UBA2 | GRCh38.p7 | 19:34428620 | TGTGGTGCGGGGGCT[A/G]GGATTCGGGGGTTCC | 10054 |
rs778610267 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462227 | CTATTAGGGAGGAGG[A/G]GATTGAGGGATTTTT | 10054 |
rs778617351 | snp | C/G | 5.03681e-05 | 0.00501812 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450352 | TTGGACTGGGCTGAA[C/G]TACAAAGTCAAGGTA | 10054 |
rs778745206 | snp | A/G | | | | | GRCh38.p7 | 19:34444515 | AGCTTTCAGAAACTA[A/G]GTTACAACAGGCCAG | 10054 |
rs778804340 | snp | C/T | 2.05324e-05 | 0.00320403 | intron-variant | UBA2 | GRCh38.p7 | 19:34469014 | CGCTTTTACCCATTT[C/T]CTTTTTCCCTTTTTT | 10054 |
rs778845283 | snp | C/G | 2.42904e-05 | 0.00348491 | utr-variant-5-prime, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428389 | TCCGGCCGCGGCTCG[C/G]TTCTCCCGCCTCCGC | 10054 |
rs778908683 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439587 | CTAATCCCAGCACTG[A/T]GGGAGGGTGAGATGG | 10054 |
rs779010147 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34453790 | GCCTCAACCTACTAA[A/G]TTGCTTGAGACTACA | 10054 |
rs779026330 | snp | A/G | 3.31581e-05 | 0.00407161 | intron-variant | UBA2 | GRCh38.p7 | 19:34450231 | TATCAATTAGGGATT[A/G]TGGGGTTCATGGGAT | 10054 |
rs779037441 | snp | C/G | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34452025 | AATGAACCCCAGTTA[C/G]GCCTGAAAGACCAGC | 10054 |
rs779082465 | snp | C/T | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34438653 | TTCATAGGGTGTGAC[C/T]GAGTGTTATGAGTGT | 10054 |
rs779117901 | snp | A/G | 1.65176e-05 | 0.00287376 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466985 | TAACCAATGGCAGTG[A/G]TGATGGAGCTCAGCC | 10054 |
rs779182762 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458843 | TCCTCCCAACCCCAA[C/T]TGTTATGTATGTGCC | 10054 |
rs779266686 | in-del | -/T | 0.0762157 | 0.179719 | intron-variant | UBA2 | GRCh38.p7 | 19:34460452 | TAATATTTTGAATCC[-/T]TTTTTTTTTTTTTGT | 10054 |
rs779298946 | in-del | -/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34429575 | TGTATGGATGAAGGC[-/T]TTGAATTAAGGGAGG | 10054 |
rs779300437 | in-del | -/T | 0.00161365 | 0.0283588 | intron-variant | UBA2 | GRCh38.p7 | 19:34451965 | AATTTCTAATATATA[-/T]TATTTTTTTCTTTAG | 10054 |
rs779311373 | snp | A/G | 6.48782e-05 | 0.00569516 | intron-variant | UBA2 | GRCh38.p7 | 19:34454601 | ACCCCCCTTAAAAAA[A/G]TCATTAATTAAAAGT | 10054 |
rs779367603 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445866 | TCAGTAGTATATACT[A/G]TTTGCCTGTTAAATA | 10054 |
rs779369453 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34432060 | AGTGGTGGTTTCTGC[C/T]TACAGAGTGGCATTC | 10054 |
rs779622483 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441208 | GCCTGTAATCCCAGC[-/A]ACTTTGGGAGGCTGA | 10054 |
rs779625426 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34460975 | GAAATTCAGTGCCCG[A/G]TTTTGGCTTTCTGAT | 10054 |
rs779648958 | snp | A/G | 1.70081e-05 | 0.00291612 | intron-variant | UBA2 | GRCh38.p7 | 19:34445171 | GTATTGTTGTGCATA[A/G]ATGTATTGTTCTAGT | 10054 |
rs779717895 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462012 | TGAAACAACCTAAAC[G/T]GCCTTGGGAGTGGCC | 10054 |
rs779763810 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34442285 | CAGCATTTTTCACTC[A/G]AAGGGAAACCTAAAT | 10054 |
rs779774514 | snp | C/G | 0.000124123 | 0.00787695 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428522 | GGGCGGCATCGGCTG[C/G]GAGCTCCTCAAGAAT | 10054 |
rs779822348 | snp | A/T | 8.29084e-05 | 0.00643796 | intron-variant | UBA2 | GRCh38.p7 | 19:34433333 | TTGGTGACCTTTTTT[A/T]ATTTTGTTTTGTAGC | 10054 |
rs779858360 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439394 | CTGATAATGATGAAA[A/G]TGCTATACCAGAATG | 10054 |
rs779869491 | snp | G/T | 1.74662e-05 | 0.00295513 | intron-variant | UBA2 | GRCh38.p7 | 19:34431946 | AGTATGCTATAGTGA[G/T]TACATTGCAAAGTTG | 10054 |
rs779877900 | snp | C/G | 1.6504e-05 | 0.00287258 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34450320 | AACTATGGCGGAAAA[C/G]GAAACCTCCAGTTCC | 10054 |
rs779938078 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451608 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 10054 |
rs779952020 | snp | C/T | 3.31027e-05 | 0.0040682 | intron-variant | UBA2 | GRCh38.p7 | 19:34452151 | ATATGGGATAAGGTT[C/T]GTTTTGACAATGTGT | 10054 |
rs780105492 | snp | A/G | | | intron-variant, downstream-variant-500B | UBA2 | GRCh38.p7 | 19:34467689 | GCTGAGGCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 10054 |
rs780110047 | in-del | -/ACCTAA | 1.85407e-05 | 0.00304467 | intron-variant | UBA2 | GRCh38.p7 | 19:34450392 | TTTTAGTCTTGGAAC[-/ACCTAA]GCTGGAAATATCCTC | 10054 |
rs780134179 | in-del | -/T/TT/TTT | 0.503902 | 0.144342 | intron-variant | UBA2 | GRCh38.p7 | 19:34460451 | TAATATTTTGAATCC[-/T/TT/TTT]TTTTTTTTTTTTTTG | 10054 |
rs780144465 | snp | A/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34439448 | AAGTTACAGATTTAC[A/C]TACATGAAGAAAGGC | 10054 |
rs780152033 | snp | A/G | 3.29641e-05 | 0.00405968 | intron-variant | UBA2 | GRCh38.p7 | 19:34431820 | AGATTTCAGATAGGA[A/G]CAGAAATATTGTAGT | 10054 |
rs780215564 | snp | A/G | 1.65029e-05 | 0.00287248 | missense, utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34466963 | GCTGAAGATGCTGCC[A/G]AAAGCATAACCAATG | 10054 |
rs780222517 | snp | C/G | 0.000149094 | 0.00863278 | intron-variant | UBA2 | GRCh38.p7 | 19:34454365 | AAATGTAAGTTATTT[C/G]TACTAAAGTTGTATC | 10054 |
rs780233262 | snp | C/G | 1.64798e-05 | 0.00287047 | intron-variant | UBA2 | GRCh38.p7 | 19:34438637 | TTTCTCATATCCTGA[C/G]TTCATAGGGTGTGAC | 10054 |
rs780315112 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34451839 | GCGTGAGCCACCGTG[C/T]CTGGCCCCATGATAA | 10054 |
rs780319099 | snp | A/G | | | intron-variant, synonymous-codon, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34430183 | CAAAGTGTTGGGATT[A/G]CAGGTATGAGCCACC | 10054 |
rs780320490 | snp | C/G | 1.82367e-05 | 0.00301961 | intron-variant | UBA2 | GRCh38.p7 | 19:34428603 | GCGCGTGAATGGCGG[C/G]CTGTGGTGCGGGGGC | 10054 |
rs780453380 | snp | A/G | 6.81052e-05 | 0.00583506 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34434957 | CTTGGACAAGTAACT[A/G]CTATCAAAAAGGTAA | 10054 |
rs780462629 | snp | A/G | 1.82503e-05 | 0.00302073 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469243 | ATGCCTCTAAACAGA[A/G]CCCTCTTACTATTTA | 10054 |
rs780633385 | snp | C/T | 1.64803e-05 | 0.00287052 | synonymous-codon, intron-variant, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34458909 | TAAAGTGACTGTTCT[C/T]ACCTTACAAGACAAG | 10054 |
rs780645837 | snp | A/G | 0.000108227 | 0.00735539 | intron-variant | UBA2 | GRCh38.p7 | 19:34454581 | TCTGTTTGCATTTTT[A/G]TGCAACCCCCCTTAA | 10054 |
rs780691089 | snp | C/G | 1.96227e-05 | 0.00313224 | missense, intron-variant | UBA2 | GRCh38.p7 | 19:34460509 | GTAGCACCAGATGTC[C/G]AAATTGAAGATGGGA | 10054 |
rs780740889 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34457456 | AGCCCAGGTATTAAT[A/G]GTGGTAGCAATTGCT | 10054 |
rs780801172 | snp | C/G | | | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34445044 | AGAGCATCTAATGAA[C/G]ATGGTGACATTAAAC | 10054 |
rs780852819 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34459392 | TTTTGGTTTCTCTGC[A/G]TGTTGGACAGTGCCC | 10054 |
rs780926045 | snp | C/T | 1.65971e-05 | 0.00288067 | intron-variant | UBA2 | GRCh38.p7 | 19:34444990 | AAATAAAATAATGAT[C/T]GTTTTATAGGGGAAC | 10054 |
rs780977140 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant | UBA2 | GRCh38.p7 | 19:34431843 | ATTGTAGTAATTCAG[C/T]GTTGTTTATTTTTCC | 10054 |
rs781017665 | snp | C/G/T | 3.37298e-05 | 0.00410658 | intron-variant | UBA2 | GRCh38.p7 | 19:34431943 | TGAAGTATGCTATAG[C/G/T]GATTACATTGCAAAG | 10054 |
rs781020667 | snp | C/T | 1.97416e-05 | 0.00314172 | intron-variant | UBA2 | GRCh38.p7 | 19:34451975 | TATATATATTTTTTT[C/T]TTTAGGAGAAGAAAC | 10054 |
rs781095906 | snp | C/G | 2.09703e-05 | 0.00323801 | intron-variant | UBA2 | GRCh38.p7 | 19:34469008 | CTCCCACGCTTTTAC[C/G]CATTTTCTTTTTCCC | 10054 |
rs781128434 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465295 | CATAGTGTTGGTGTG[A/G]TTATTTGGAGAGAAC | 10054 |
rs781185008 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437871 | ACCAAGCTGGCCAAC[A/G]TGGAAAAACCCCGTC | 10054 |
rs781202812 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34430012 | CGCCTCCCAGGCTCC[A/G]GTGATCCTCCACCTC | 10054 |
rs781207280 | in-del | -/GC | 2.44275e-05 | 0.00349473 | intron-variant | UBA2 | GRCh38.p7 | 19:34428582 | CCTGGTGAGGGCCGG[-/GC]GCGCGCGCGTGAATG | 10054 |
rs781220012 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34448749 | GAGGTTTCAACTAGG[G/T]ATATGGTTGGGATTC | 10054 |
rs781231147 | in-del | -/C | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431243 | CTATCATTTTCTTTT[-/C]CTTTTTTTTTTTTTT | 10054 |
rs781313344 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449856 | CCATGAGCTTGGAGG[C/T]ATTGCTGACTGGCAT | 10054 |
rs781352231 | snp | A/G | 3.42214e-05 | 0.00413637 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34434870 | GTTTTACTTCCAGCT[A/G]CCCGAAACCATGTTA | 10054 |
rs781359800 | snp | A/G | 1.68315e-05 | 0.00290094 | missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469102 | TCTTCAAATAATGCC[A/G]ACGTCAGTGAAGAAG | 10054 |
rs781406807 | in-del | -/TT | | | intron-variant | UBA2 | GRCh38.p7 | 19:34445437 | CTTCTCATCTTCACT[-/TT]TTTTTTTTTTTTTTT | 10054 |
rs781455778 | snp | C/T | 5.0606e-05 | 0.00502995 | intron-variant | UBA2 | GRCh38.p7 | 19:34445157 | AATCATGGATAGATG[C/T]ATTGTTGTGCATAGA | 10054 |
rs781472157 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456857 | GCCACCGTTCCTGGC[C/T]GATACCCAGTTTTTA | 10054 |
rs781537032 | snp | C/G | 0.000115276 | 0.00759109 | synonymous-codon, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428501 | CCGGGTGCTGGTGGT[C/G]GGGGCGGGCGGCATC | 10054 |
rs781585024 | snp | C/G | 1.64972e-05 | 0.00287199 | intron-variant | UBA2 | GRCh38.p7 | 19:34438615 | AACTGCCATCATGGA[C/G]TAAATTTTTCTCATA | 10054 |
rs781588563 | snp | C/T | 2.09369e-05 | 0.00323543 | utr-variant-5-prime, missense, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428416 | CCGCCTCCGCCGCGG[C/T]TCGTGGTTGTCCCGC | 10054 |
rs781698445 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469315 | AAGGGAAAAAATTGA[C/T]AGCAGTGACTTGAAA | 10054 |
rs781699500 | snp | A/C/G | 0.000108418 | 0.00736201 | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469236 | AACAGAAATGCCTCT[A/C/G]AACAGAACCCTCTTA | 10054 |
rs781729755 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34436382 | TCAGCTCGCCGCAAC[C/T]TCCGTCTCCCTGGTT | 10054 |
rs781736251 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34433816 | ACACAAAAATTAGCC[A/G]GTGTGGTGGCATGTG | 10054 |
rs781755246 | snp | A/C | 1.66774e-05 | 0.00288763 | intron-variant | UBA2 | GRCh38.p7 | 19:34452179 | TGTGGCAAGTACTTA[A/C]ATGTCAAAAGTGTGT | 10054 |
rs781770651 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34469769 | GTACCGCCTGGTATG[C/T]CTGTGTAAGAAGCCA | 10054 |
rs796095920 | snp | A/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34456091 | CCGATGCGCTCTTTT[A/T]TTCCTTTTCTTTTTC | 10054 |
rs796224307 | snp | G/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34458193 | GTTGCAGAAGAACGC[G/T]GAGTCTTATATAATA | 10054 |
rs796382180 | in-del | -/A | | | intron-variant | UBA2 | GRCh38.p7 | 19:34437781 | AAATGGGCTGGGCGC[-/A]AGTGGCTCACGCCTG | 10054 |
rs796393606 | snp | C/T | | | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | UBA2 | GRCh38.p7 | 19:34428386 | GCTTCCGGCCGCGGC[C/T]CGGTTCTCCCGCCTC | 10054 |
rs796689375 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34431778 | GGTACTATGTAAGTA[A/G]ATAACAGCATTGTGG | 10054 |
rs796691817 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34462802 | AAAACCTCATCTCTT[A/G]TAAAAATACAAAAAT | 10054 |
rs796851360 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34441449 | GACAGAGCGATACTC[C/T]GTCTCAAAAAAATAA | 10054 |
rs796868543 | in-del | -/AG | | | intron-variant | UBA2 | GRCh38.p7 | 19:34465618 | TCCAGCCTGGGCGAC[-/AG]AGGGGGACTCCATGT | 10054 |
rs796935522 | snp | C/T | | | intron-variant | UBA2 | GRCh38.p7 | 19:34438333 | GTCTTTCCAGTAGTT[C/T]TTCTGTTTAGTGTGA | 10054 |
rs797017010 | snp | A/G | | | intron-variant | UBA2 | GRCh38.p7 | 19:34449783 | AAGATATCGCAGTTC[A/G]GAAGTTCTGTTGTGA | 10054 |