SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs191026455 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490536 | CATATGCTCCTCACA[A/G]CAACCCTGTGAGGTG | 89910 |
rs191030526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532705 | CTGCCGCTTGGAGAA[C/T]GCCGGGAGTTCCCAG | 89910 |
rs191032230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109509362 | TGCACCTGTCACCCC[A/G]TCATCTAGGTTTTAA | 89910 |
rs191041722 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109505946 | TTCTGAGGAACACAC[C/T]TTAATGTATATTCAG | 89910 |
rs191147864 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508679 | GAGGCAAGAGCAGGG[G/T]TCTAGCTGCTGGTGA | 89910 |
rs191152653 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109484101 | TCACCCTCACATCCT[C/G]TCCCTTTTGTTTTCT | 89910 |
rs191257443 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109490205 | GGACAGTGGTGCTGG[A/G]ATCCCTTGAATGCTC | 89910 |
rs191271992 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519889 | GCCTAACCCCTGAAT[A/C]GGGGCACCATAGGAT | 89910 |
rs191277164 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109493229 | TACCCAAGTCACCTT[A/G]TGGGGCAGCTCATTC | 89910 |
rs191288751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513597 | ATGAAAAAAGTTACT[G/T]CAGTGATAGAGGTGC | 89910 |
rs191308411 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535341 | TGCTGCCCAGGGAAG[C/T]GCAGGCGCCTGCTAG | 89910 |
rs191431176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495519 | AGACCCTAACCCAGC[A/G]GCACTAGAGGAATTA | 89910 |
rs191437839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538314 | GCTTATCTCCTGGAA[A/G]CTTATCAAATTGGCC | 89910 |
rs191451600 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477799 | GGTAGGGCCTGCGGT[C/G]CGGCCTGCGGGAGAA | 89910 |
rs191455725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538783 | ACATTCCCTCATCCA[C/T]ACTGCCGCCTCTGAG | 89910 |
rs191465272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109518531 | AGGGACTCCCTTTCT[A/G]GCACTTCCCTCTGCA | 89910 |
rs191523717 | snp | A/G | 0.000910332 | 0.0213152 | intron-variant | UBE3B | GRCh38.p7 | 12:109485998 | TGTATAACCCCCAGT[A/G]TGTCTCTTTGCAGAG | 89910 |
rs191554789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518099 | GTCTCATTACAGGAG[A/C]ATTCTGTTTGCGTGC | 89910 |
rs191582739 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524723 | CTTCCCGCAGAGACC[C/T]TGCTTTCTTATATCG | 89910 |
rs191594782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533230 | CACAAGTGGCCAGTC[A/G]CACCTATTGGGTATG | 89910 |
rs191596382 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109491769 | GTCATGGTGGAACCA[A/G]CTTGGTGAAAGCTGC | 89910 |
rs191654024 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485619 | TTTGGCTACTGGCTG[G/T]GAGGCAAAAGTCAGT | 89910 |
rs191781825 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109492442 | CACAGTTAGAGCCAC[A/T]TTTAAAAAGCCAAAA | 89910 |
rs191799657 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477738 | TGCGGCCCCGACCCC[A/C]AGTGCGGGGACCTCC | 89910 |
rs191818925 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476090 | AAATCATTAGTCTAA[G/T]CCCTTGCAGGGCTTG | 89910 |
rs191861033 | snp | C/T | 0.00348138 | 0.041576 | intron-variant | UBE3B | GRCh38.p7 | 12:109510310 | TCTCTGGCTCTGACT[C/T]CTCCTCTGACTTTCC | 89910 |
rs191866960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109541207 | AGACAGGCTAGGATC[C/T]TGCAGGCAGCAGGGG | 89910 |
rs191928670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517093 | TGCTGGAGACCCAGC[A/G]GTGTCTTCCTTTACC | 89910 |
rs191935084 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479339 | TTAATCCTAATCACA[A/G]TGTTGTGATGACTAA | 89910 |
rs191939387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528265 | CATACTCTCTTCTCT[C/T]GTATCTCCCTCTCTC | 89910 |
rs191972425 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497051 | GTCTGTGGCTCATTT[A/C]ATTATTTTTTATATA | 89910 |
rs191985156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520330 | CAGAAGCCAGGAAGG[C/T]CTCAACAGATTAGAA | 89910 |
rs192106134 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UBE3B | GRCh38.p7 | 12:109484667 | AGTGCTGGGATTACA[C/G]GCGTGAGCCACTGTA | 89910 |
rs192120537 | snp | C/T | 3.29968e-05 | 0.00406169 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524467 | CATCACTGACCTGGG[C/T]CTGACGCTGTCTTAC | 89910 |
rs192138893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109502320 | CACTGAACCACAGGC[A/G]GGGCTAGCGCTTCAG | 89910 |
rs192260574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494734 | GTTTGCAGTGTGTGT[A/G]GTTTTTTGAGTCTGG | 89910 |
rs192277830 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109537991 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCAACATT | 89910 |
rs192368208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109488017 | AGCAGCCAACATTAC[A/G]TGGAGTTATCTATGT | 89910 |
rs192483866 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109529608 | CTCCTTGTGATTCCC[A/G]ACATAGTGGGGGCTT | 89910 |
rs192640331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485338 | CGGGCAAGATCTCTA[C/T]GCTCATGGAGCTCAT | 89910 |
rs192694454 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109512173 | GGGAGAGCACCCAAA[G/T]CTCCTGACTGCCCCC | 89910 |
rs192723804 | snp | A/G | 0.000596044 | 0.017253 | intron-variant | UBE3B | GRCh38.p7 | 12:109507551 | AGCTTGGGTTTCTCT[A/G]TGTTTTTTCCAGGTC | 89910 |
rs192805046 | snp | C/T | 0.000186338 | 0.00965061 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534621 | CTGGGCAGCGTCCTC[C/T]GGGGCTTCTTCACCA | 89910 |
rs192840623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109506932 | AAATAAGGCAAAGCC[A/G]AGGTGTAACCAGTCA | 89910 |
rs192850952 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109539479 | AACCCCAGCTCTGCC[A/G]CCCACGATCTGGGAG | 89910 |
rs192868868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109533823 | GAGTGGGGGTGGGTA[C/T]GTGCTGTTTTTAGTG | 89910 |
rs192873361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502804 | GGCTTATTCTGAGAA[A/G]TATTTGGGTATTCTG | 89910 |
rs192919618 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494266 | CTCTTTCTTCTTATT[A/C]TTTGTACTTGCCTCA | 89910 |
rs192977667 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535691 | CATCCCATCTGGGCG[A/G]TGGCTTCACTCCTGA | 89910 |
rs193042160 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109487342 | ACTTCCACTTTGCTT[A/G]TAAGGATAGAGAGGT | 89910 |
rs193060858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520157 | TTGTTCCATCACAGT[A/G]TCTGAAGACATCAGT | 89910 |
rs193091424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478321 | ATTCTGTGAACGGGG[A/G]AGCCCTGGATCTTGT | 89910 |
rs193195960 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109514737 | CATTCCTATCACCAG[C/T]CTCCCTCCCTGTGTC | 89910 |
rs193234555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539166 | GCTTGAACCCAGGAG[C/G]CGGAGGTTGCAATGA | 89910 |
rs193250109 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109496248 | CATGGATCAGTACTT[A/C]ATGCATTTTATGGCC | 89910 |
rs199551591 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | UBE3B | GRCh38.p7 | 12:109481526 | CCCAGTGGTGTTTTT[-/A]AAAAACCATTGGCAT | 89910 |
rs199605739 | snp | A/C | 1.65734e-05 | 0.00287862 | intron-variant | UBE3B | GRCh38.p7 | 12:109523953 | ATCCTGGCTGATGGA[A/C]AGCTCTGCTTCTCTG | 89910 |
rs199651712 | snp | C/T | 1.68949e-05 | 0.0029064 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477225 | GCTCCCTCGGCCGCC[C/T]TCAACCCCTAGTCCA | 89910 |
rs199655024 | snp | A/G | 9.88435e-05 | 0.00702937 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109489931 | TAGGTGAAAGTCTTC[A/G]ACCAGCGATGAACCA | 89910 |
rs199656810 | in-del | -/ATAAG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519886 | AAGCCTAACCCCTGA[-/ATAAG]ATCGGGGCACCATAG | 89910 |
rs199680941 | snp | A/G | 1.65203e-05 | 0.002874 | intron-variant | UBE3B | GRCh38.p7 | 12:109501340 | GCATCAGATGGAACT[A/G]ACAGACCAGGTCTCC | 89910 |
rs199696846 | snp | A/G | 0.00022192 | 0.0105314 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510422 | ACGAGCGGGACTGCC[A/G]GCGGCGCTTCACCCC | 89910 |
rs199700946 | in-del | -/CA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527734 | GGGCCCAGCCAGGGC[-/CA]GAGAGAGAGCATGGT | 89910 |
rs199720082 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483789 | GTTTTTTCTCATAAA[-/A]GTGCTTGAAAAGCCT | 89910 |
rs199843612 | in-del | -/TCCTGCTGTAA | 0.00597247 | 0.0543191 | intron-variant | UBE3B | GRCh38.p7 | 12:109487067 | GGTCACCTCGTCCTT[-/TCCTGCTGTAA]TCATGGCAACGAGCA | 89910 |
rs199869687 | in-del | -/G | 0.0770498 | 0.180522 | intron-variant | UBE3B | GRCh38.p7 | 12:109515367 | TATTACTGTTTTTTT[-/G]TTGTTGTTGTTGTTG | 89910 |
rs199888518 | in-del | -/AA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109492738 | CAAAAAAAAAAAAAA[-/AA]GTCAAAATAAAAGGG | 89910 |
rs200095998 | snp | C/T | 4.94246e-05 | 0.0049709 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488659 | ACGTGGAAAATTCTT[C/T]GGGGAAAAGGTCTGT | 89910 |
rs200114053 | snp | G/T | 8.34341e-05 | 0.00645834 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483663 | GCTGTTGTGATCCAG[G/T]CCCATGTCCGGAGTT | 89910 |
rs200182141 | snp | C/T | 0.000115305 | 0.00759205 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109529972 | CTCATTAGCGGATTC[C/T]GTTCCATTATCAAAC | 89910 |
rs200207745 | snp | A/C | 0.00199792 | 0.0315431 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491068 | AACCCGTGGCCTGGC[A/C]AGACCCCGTCCTTGT | 89910 |
rs200222959 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507981 | CAGTACCACTGGCTG[G/T]GGCTTGGGGTCTCCT | 89910 |
rs200272943 | snp | C/T | 3.2994e-05 | 0.00406152 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483869 | TTTCTAGGAGAGAGA[C/T]TGATGACTTTTTTAA | 89910 |
rs200295015 | snp | C/T | 0.000138218 | 0.00831204 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510401 | ACGGGTGGCTTATGG[C/T]GCTGTACGAGCGGGA | 89910 |
rs200296256 | snp | A/G | 0.000115682 | 0.00760446 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511275 | AGTTGATCCTGCAGT[A/G]CATCCCACATGTCAT | 89910 |
rs200342908 | snp | A/G | 3.94501e-05 | 0.00444111 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510405 | GTGGCTTATGGTGCT[A/G]TACGAGCGGGACTGC | 89910 |
rs200362048 | snp | C/T | 0.000131778 | 0.00811614 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497855 | TCAGACAATCTGATT[C/T]GGCCGTTCCTCATCC | 89910 |
rs200389976 | snp | A/G | 0.000101058 | 0.00710765 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534661 | GGGAGCCAGGCGGCC[A/G]CCTGCCCACCTCCTC | 89910 |
rs200429727 | snp | A/C/G | 3.29458e-05 | 0.00405857 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488594 | TCCTGCAGGACTCCC[A/C/G]ACTCATCACCCTGTA | 89910 |
rs200433175 | snp | A/G | 0.00013224 | 0.00813035 | intron-variant | UBE3B | GRCh38.p7 | 12:109524143 | TGGTGGGTGAGCTAA[A/G]CCGAGCACTGGTGTG | 89910 |
rs200514073 | snp | A/G | 1.69683e-05 | 0.00291271 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499680 | AGAGTGTTAGAGGAG[A/G]AGACAGATGGGTTCG | 89910 |
rs200541587 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539241 | CTCCGTCTCAAAAAC[-/A]AAAAAAACCCCACAA | 89910 |
rs200548330 | snp | A/G | 0.000512545 | 0.0160003 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533549 | CTGCGTGGAGGTGTC[A/G]GACGATCAGGTACCC | 89910 |
rs200710207 | in-del | -/T | 0.116916 | 0.211633 | intron-variant | UBE3B | GRCh38.p7 | 12:109521560 | TATGAGGTAGGAACG[-/T]TTAAGAAACAGAGAA | 89910 |
rs200727329 | snp | G/T | 0.00171824 | 0.0292603 | intron-variant | UBE3B | GRCh38.p7 | 12:109530087 | AGTAAGAGGCGGGTG[G/T]GGGGAAGGGTGAAAT | 89910 |
rs200771801 | snp | A/G/T | 8.26008e-05 | 0.00642607 | intron-variant | UBE3B | GRCh38.p7 | 12:109501330 | CCCTGGCCCTGCATC[A/G/T]GATGGAACTGACAGA | 89910 |
rs200787724 | snp | A/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498309 | AAGATCGATGCCGTG[A/T]TGTATGTGAAAGTTT | 89910 |
rs200794116 | in-del | -/T | 0.0810589 | 0.184279 | intron-variant | UBE3B | GRCh38.p7 | 12:109488402 | CCACATTCCCTGTTA[-/T]TTTAACTCCTGGAGT | 89910 |
rs200796822 | snp | A/G | 3.57654e-05 | 0.00422864 | intron-variant | UBE3B | GRCh38.p7 | 12:109521565 | AGGTAGGAACGTTAA[A/G]AAACAGAGAAATGTA | 89910 |
rs200838466 | snp | C/G/T | 0.000152131 | 0.00872048 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477241 | TCAACCCCTAGTCCA[C/G/T]GGGCACCGCCCTCCC | 89910 |
rs200878507 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524082 | ACTGCCTTCTCTGGA[C/T]TCCGAGTTCTATAAA | 89910 |
rs200936935 | snp | A/G/T | 4.95678e-05 | 0.00497814 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486542 | GATCAAGAACATTTT[A/G/T]TGGTACTGCTGTGAT | 89910 |
rs200964637 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483904 | GATGACCCTGAGTCC[A/G]CTAAAAGAAGTGCAC | 89910 |
rs201028903 | snp | C/T | 0.000529267 | 0.0162589 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499714 | GTTTGCTCACCCAGA[C/T]GCTGTGCTACTGTCG | 89910 |
rs201030846 | in-del | -/CCAGGGTGCAGAT | 0.00478085 | 0.0486577 | intron-variant | UBE3B | GRCh38.p7 | 12:109508073 | ATTCCAAAGTCAGAG[-/CCAGGGTGCAGAT]CCTTGCTAAGCAGAT | 89910 |
rs201045720 | in-del | -/AATT | 0.200801 | 0.245111 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475536 | GCTACACCCCAGATC[-/AATT]AATCAGTATCTCAGA | 89910 |
rs201130963 | snp | A/G | 4.94605e-05 | 0.0049727 | intron-variant | UBE3B | GRCh38.p7 | 12:109503195 | GATACTCACAGGTTC[A/G]CAGTCCCCAGGGCAT | 89910 |
rs201190797 | snp | A/G | 0.000102575 | 0.00716078 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509747 | TGCTGTTGTTTGGTT[A/G]ATGCTGCACCCAGGG | 89910 |
rs201191919 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109485241 | CCAAGTTACCAGCTG[A/T]TAGGCTGTTAGGCAT | 89910 |
rs201226299 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | UBE3B | GRCh38.p7 | 12:109541541 | TTCTTCCTTGGCCTT[-/G]GGGCCAGGCAGGGTG | 89910 |
rs201243745 | snp | A/C/G/T | 0.000973488 | 0.0220434 | intron-variant | UBE3B | GRCh38.p7 | 12:109490023 | TGTGACTCCTGCCCC[A/C/G/T]CAGTGTGCAACTTCT | 89910 |
rs201300822 | snp | C/G | 0.000683463 | 0.0184733 | intron-variant | UBE3B | GRCh38.p7 | 12:109510484 | GGGGTGAGGAGGGCT[C/G]CATGGAAGCCAGCCT | 89910 |
rs201326766 | in-del | -/T | 0.00317509 | 0.0397173 | intron-variant | UBE3B | GRCh38.p7 | 12:109526335 | AGTCCTCCCTATTAA[-/T]TTACTCCCATCTTCT | 89910 |
rs201336062 | in-del | -/AAAAAAAA | 0.373397 | 0.217424 | intron-variant | UBE3B | GRCh38.p7 | 12:109486581 | GCAGCTCAAGGTAAC[-/AAAAAAAA]AAAAAAAAAAAAAAA | 89910 |
rs201364013 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109485848 | CCCTTTAGTCTTTAT[C/G]ATCTTCAGTGTCCTC | 89910 |
rs201398969 | snp | A/C | 0.000115878 | 0.00761088 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483961 | CTGCTGTTCCTATTC[A/C]GAATCAAAGAGGATA | 89910 |
rs201440748 | in-del | -/CTT | 0.0341408 | 0.126114 | intron-variant | UBE3B | GRCh38.p7 | 12:109519780 | TGTACATAAAAAGTC[-/CTT]CTCAGGTTTGCCTCC | 89910 |
rs201525907 | snp | A/G | 0.000891943 | 0.0210992 | intron-variant | UBE3B | GRCh38.p7 | 12:109498364 | AATGGGTAAGTATCC[A/G]TGGCTGGAACTTGAT | 89910 |
rs201572763 | snp | G/T | 4.94189e-05 | 0.00497062 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524047 | CACCACCACAGCGTC[G/T]TCTATAGCTCGGTGG | 89910 |
rs201620860 | snp | A/G | 0.00043562 | 0.014752 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483673 | TCCAGGCCCATGTCC[A/G]GAGTTTTCTCTGTCG | 89910 |
rs201631937 | snp | C/T | 6.64794e-05 | 0.00576501 | intron-variant | UBE3B | GRCh38.p7 | 12:109498403 | GGCCATCAGGGAAAG[C/T]CCGAGTGTTTTGCCT | 89910 |
rs201644978 | snp | C/T | 4.94947e-05 | 0.00497443 | intron-variant | UBE3B | GRCh38.p7 | 12:109501368 | TCCTCTGCTCTCTCC[C/T]AGCCTTAACGAGTCA | 89910 |
rs201692069 | snp | A/G | 0.000230635 | 0.0107361 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488660 | CGTGGAAAATTCTTC[A/G]GGGAAAAGGTCTGTG | 89910 |
rs201706780 | in-del | -/AC | 0.0123036 | 0.0774623 | intron-variant | UBE3B | GRCh38.p7 | 12:109543388 | GGTCAGCGGCTGGTA[-/AC]ACAGCAGGACTCGGC | 89910 |
rs201712288 | snp | C/T | 3.32718e-05 | 0.00407858 | intron-variant | UBE3B | GRCh38.p7 | 12:109524511 | TGGGTCAGGTAGGTC[C/T]GCCCTTTGGCTGAGC | 89910 |
rs201722927 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477237 | GCCCTCAACCCCTAG[A/T]CCATGGGCACCGCCC | 89910 |
rs201925415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109538517 | TCCCCTCCAGAGCAC[A/G]TGAGGATTAAATGCA | 89910 |
rs201964985 | snp | G/T | 9.06396e-05 | 0.00673139 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534798 | CTCCTGTCCCAGCCC[G/T]GCCTCCAGGGCTCCT | 89910 |
rs202119239 | snp | C/T | 0.001239 | 0.0248589 | intron-variant | UBE3B | GRCh38.p7 | 12:109516747 | CCTGTTTTCTGATCC[C/T]GCCTTTGTTCATTTT | 89910 |
rs202144137 | snp | C/T | 0.000527001 | 0.0162241 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530026 | ACTCCTGAACTGCAG[C/T]GTCTCATCTCTGGCG | 89910 |
rs202210474 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534602 | TCAGGACACCGGGGA[C/T]ACTCTGGGCAGCGTC | 89910 |
rs367696294 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508037 | GCCATTTATTCACTG[A/T]GCTAGCTAGATTCCT | 89910 |
rs367761514 | in-del | -/AA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480651 | GCGAGACCCTGCCTT[-/AA]AAAAAAAAAAAAGAC | 89910 |
rs367768757 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488232 | CCTAGTCATGCTCAA[C/T]TGCATTTCTGCTCTG | 89910 |
rs367828195 | snp | C/T | 3.62911e-05 | 0.0042596 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534803 | GTCCCAGCCCTGCCT[C/T]CAGGGCTCCTGGGCT | 89910 |
rs367891553 | in-del | -/C | 0.00438332 | 0.0466095 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536144 | CATCCTGGTGTCCCA[-/C]CCAGGTCGAGCCCCC | 89910 |
rs367916038 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476364 | GATTTTCCCTTAAGA[A/C]TGCACTTTCCAGGGA | 89910 |
rs367936977 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537577 | CGCAGGCGTCCTCAC[A/G]AGGAGCGTTCATGTA | 89910 |
rs367953530 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109498953 | ACCTCAGCCTCCTGA[A/G]TAGCTGGGACTACAA | 89910 |
rs367971212 | snp | A/G | 1.65411e-05 | 0.00287581 | intron-variant | UBE3B | GRCh38.p7 | 12:109503234 | CCTCTCACATTTGGC[A/G]GACAGTTTGTCTTAG | 89910 |
rs368097236 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530647 | CCGGATGAGAGAGCT[A/G]TGTTTCTGAAGGTAT | 89910 |
rs368120913 | snp | A/G | 1.71749e-05 | 0.00293038 | intron-variant | UBE3B | GRCh38.p7 | 12:109483738 | GGATCTCCCTAGCAC[A/G]TGATTCTCTGGCTCC | 89910 |
rs368149678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109497716 | TTCTCAGAAATCCCA[C/T]GCAGAATAATTTCTA | 89910 |
rs368155159 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508398 | AAGTGAAAAAAACAG[C/T]GTCAAATACTTAGTG | 89910 |
rs368214041 | snp | C/T | 6.58968e-05 | 0.00573969 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497917 | TCTCAGCACAGTGAC[C/T]CCTGAGGTAAGCAGG | 89910 |
rs368215388 | snp | C/T | 3.30136e-05 | 0.00406273 | intron-variant | UBE3B | GRCh38.p7 | 12:109523970 | GCTCTGCTTCTCTGC[C/T]CTCCCAGGGAATTGT | 89910 |
rs368299416 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516542 | CAGACCACTCTTTCC[A/G]GAACGTTTTTTGCTT | 89910 |
rs368343229 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494240 | CAGGCTATTTAACTC[C/T]AGAACTCATACTCTT | 89910 |
rs368350404 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3B | GRCh38.p7 | 12:109532772 | CCCACTTGGGCTGCC[A/G]GCACCTCAGCCTGCT | 89910 |
rs368398958 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476140 | TCCACCCCAAGAATG[A/T]CTGATTCAGTAGTCT | 89910 |
rs368428917 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109493639 | GAACACAATCAGGAC[C/T]TTTTAAAGTAAGATA | 89910 |
rs368528858 | multinucleotide-polymorphism | AT/TC | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503645 | CATGTCACAAATTCT[AT/TC]GAAAACCTTATCTTT | 89910 |
rs368536875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109528151 | GTCAGGGTAAGGATA[C/T]TCAGTTCTGCATACT | 89910 |
rs368537073 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491244 | TTTTGTCAGAATTTA[C/T]GGGAAGCATTGTTCT | 89910 |
rs368580939 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523111 | TAGGCCCTGCATGAG[A/G]AGTGGCATGGATTAA | 89910 |
rs368626531 | snp | A/G/T | 6.61436e-05 | 0.0057505 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499715 | TTTGCTCACCCAGAC[A/G/T]CTGTGCTACTGTCGG | 89910 |
rs368632031 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484160 | AGTGCTTTTAGGAAT[C/G]TTTTCACATTGACCA | 89910 |
rs368647016 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532557 | AGAAGGGAGAACATT[-/T]CTTGGCTACTGTTGA | 89910 |
rs368668526 | snp | A/C | 1.64874e-05 | 0.00287113 | intron-variant | UBE3B | GRCh38.p7 | 12:109533439 | AGGAGCCTGCCCCGT[A/C]CCCACTGACCCTGCT | 89910 |
rs368699646 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524603 | GAGCCCCAAGCTGAG[G/T]CTCTGTCTGGTCCCT | 89910 |
rs368703761 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503670 | TATCTTTATTGGCTA[A/C]ATAGTATCTCATCAC | 89910 |
rs368743705 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517020 | CTCTGGGAGCAGGAA[A/G]GGGGTCATTTGTCCT | 89910 |
rs368767023 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484377 | GCAGCTACTACACAC[C/T]TCGGTGGTGGACTCA | 89910 |
rs368805878 | snp | C/T | 0.000248092 | 0.0111348 | intron-variant | UBE3B | GRCh38.p7 | 12:109530507 | GTCCATAAGTGCCCA[C/T]GCTAGCACATTGCTG | 89910 |
rs368809737 | snp | C/T | 0.000214392 | 0.0103513 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516841 | CCAGCTCTGCCTCCC[C/T]GCATGTCACTCACAT | 89910 |
rs368887776 | snp | A/G/T | 4.94281e-05 | 0.00497112 | stop-gained, missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501418 | AGCTGCAGTTCTTGT[A/G/T]GGGGGTGCCTCTGAT | 89910 |
rs368894886 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477373 | GATAACTTCCGCTGT[C/T]CGCACCCCACTTCCG | 89910 |
rs368948769 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109502917 | TTGCCCCACTGTCTG[G/T]CCTGGCTGTGCATTT | 89910 |
rs368961114 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491516 | GAAATAATGTGAATA[C/T]GCATGTAAAATGTTA | 89910 |
rs368973418 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479974 | CATTGTGCTTGTGGC[-/T]TTGGGCCCTGCTCTT | 89910 |
rs369032099 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495610 | AGAGCTGAGAGCCTC[A/G]AACAGAGATTTACCC | 89910 |
rs369069499 | snp | A/C | 1.67139e-05 | 0.00289079 | intron-variant | UBE3B | GRCh38.p7 | 12:109516911 | GCCTATGGAATCCTA[A/C]CACAAGGAAGTGGGC | 89910 |
rs369075901 | snp | A/G | 0.00146966 | 0.0270679 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534576 | CCAATTCAAGGCCAC[A/G]ATGTGTGCCTTCAGG | 89910 |
rs369112970 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512551 | AGGAGTCTAGGTTGT[A/G]TCCTTTATTTTTCTC | 89910 |
rs369160337 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109481087 | TCCAGCCTGGGCGAC[A/G]GAGCAAGACTCCGTC | 89910 |
rs369171639 | snp | C/T | 8.27164e-05 | 0.0064305 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533552 | CGTGGAGGTGTCGGA[C/T]GATCAGGTACCCCCA | 89910 |
rs369207743 | snp | C/T | 4.94531e-05 | 0.00497234 | intron-variant | UBE3B | GRCh38.p7 | 12:109497949 | TCTGTGAGTTCCCCG[C/T]GAAAACCCAATTGTG | 89910 |
rs369239008 | snp | C/T | 0.000152229 | 0.00872303 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477256 | TGGGCACCGCCCTCC[C/T]TACCATGAAAAGTCG | 89910 |
rs369247467 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE3B | GRCh38.p7 | 12:109502975 | TCCAGGGTGGGATTT[A/G]GCAGCTGGCTGAGCT | 89910 |
rs369284447 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518600 | CCCCACTACCCATCA[C/T]GCCTACCCAGACGTG | 89910 |
rs369331660 | in-del | -/AC | 0.001691 | 0.0290282 | intron-variant | UBE3B | GRCh38.p7 | 12:109486579 | AAGCAGCTCAAGGTA[-/AC]AAAAAAAAAAAAAAA | 89910 |
rs369331998 | snp | A/G | 8.36365e-05 | 0.00646616 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486065 | GGATGCTGAGAATGA[A/G]CCTAAGGTAAGTGGA | 89910 |
rs369410122 | snp | A/G | 1.97634e-05 | 0.00314346 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510413 | TGGTGCTGTACGAGC[A/G]GGACTGCCGGCGGCG | 89910 |
rs369445751 | snp | C/T | 4.96471e-05 | 0.00498208 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507720 | TGTTCTGTGACTGTT[C/T]GCGGCACCTCATCAC | 89910 |
rs369498355 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540984 | CTCCTCTTGGGCCAC[A/G]TGAGCCCTTCTCTGC | 89910 |
rs369617790 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109518523 | TGTGTGGTAGGGACT[-/C]CCTTTCTAGCACTTC | 89910 |
rs369660865 | snp | G/T | 3.30852e-05 | 0.00406712 | intron-variant | UBE3B | GRCh38.p7 | 12:109526466 | TTGAAAAGACTTCAT[G/T]CTGGCTCTCTGCGCT | 89910 |
rs369683005 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495036 | TTAGGGAATTGTGCT[C/T]TTCTGTTTTAAACTT | 89910 |
rs369728531 | snp | A/C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477130 | CCCCTAACCAATCCC[A/C/G]CAAATGCCTCTCCAC | 89910 |
rs369731773 | snp | A/C/G | 0.000369758 | 0.0135922 | intron-variant | UBE3B | GRCh38.p7 | 12:109499606 | TGTTTGTCTGGGCCC[A/C/G]TCACACTCAGCCTTC | 89910 |
rs369743781 | snp | C/T | 3.29701e-05 | 0.00406005 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533504 | CCCGCTCCTGGGATT[C/T]GCCTACCTCAAGCCT | 89910 |
rs369745421 | snp | C/T | 0.000214445 | 0.0103526 | intron-variant | UBE3B | GRCh38.p7 | 12:109529878 | TTGTTATCTCTTCCT[C/T]GTTGGCAACAGAATT | 89910 |
rs369763096 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109524769 | ATGGTAACGAAAAGC[A/C]ATGTTACAAATGGGG | 89910 |
rs369770710 | snp | G/T | 0.000247478 | 0.011121 | intron-variant | UBE3B | GRCh38.p7 | 12:109530531 | ATTGCTGAGCCCAGG[G/T]CTGTATTGCTTTCAG | 89910 |
rs369783919 | snp | A/G | 4.94328e-05 | 0.00497131 | intron-variant | UBE3B | GRCh38.p7 | 12:109488555 | TGTCTTAATCTTGCT[A/G]TGTTTATTGTTTCCA | 89910 |
rs369808425 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBE3B | GRCh38.p7 | 12:109529128 | ATCGCACCACTGCAC[A/T]CCAGCCTGGGTGACG | 89910 |
rs369810322 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109541402 | AGCATTTCACTTCTC[C/G]GAGATTCATTTTCCC | 89910 |
rs369860465 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE3B | GRCh38.p7 | 12:109501544 | TGAAGAGTGAGTGAC[A/G]GGAGCAGGCCCAACC | 89910 |
rs369888070 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109530923 | TGTGCTCGGCACTCC[A/G]TCCTCCCCTTTGCCT | 89910 |
rs369925703 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506038 | TATACCCGTGATGTG[A/G]CCTGTGTGTCTAAGG | 89910 |
rs369927539 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | UBE3B | GRCh38.p7 | 12:109485424 | AGGACAGATAAGCTG[A/G/T]AGGAGGTGAACCTCA | 89910 |
rs369983686 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109512225 | GGGAATCAGACAGCA[A/C/T]CCAAGTCTGCTGACT | 89910 |
rs369988714 | snp | C/T | 6.75824e-05 | 0.00581263 | intron-variant | UBE3B | GRCh38.p7 | 12:109501560 | GGAGCAGGCCCAACC[C/T]TGTAGCTCCACTTGG | 89910 |
rs370005095 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525897 | GATAGTGTGTTACCT[A/G]CGTCCCTTGAGACTC | 89910 |
rs370059886 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486756 | CCTCCTTTGGTGTGT[G/T]TTGGACCCTTAAACT | 89910 |
rs370067670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479289 | TCACTTACATGCTAC[A/G]TGCTTTTAGATATCC | 89910 |
rs370069736 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE3B | GRCh38.p7 | 12:109506449 | TGCCTCCCAGGTTCA[A/G]GCGATTCTCCTGCCT | 89910 |
rs370136647 | snp | A/G | 3.32806e-05 | 0.00407912 | intron-variant | UBE3B | GRCh38.p7 | 12:109524512 | GGGTCAGGTAGGTCC[A/G]CCCTTTGGCTGAGCT | 89910 |
rs370153925 | in-del | -/GAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109498785 | GGCAGAGGCACAGAA[-/GAA]TTCTCCTTGCCTAAA | 89910 |
rs370344870 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503085 | CTCAGGCCTGTCGGG[G/T]GTAAACGGGTCGACT | 89910 |
rs370421149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109543201 | TGCGTGTGCGTGTGG[C/T]TTGTCTGAACACTGC | 89910 |
rs370431051 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482417 | CCCACTTCTAAGTGA[A/G]GTCATGCAGTATTTG | 89910 |
rs370443056 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521491 | CACATCCTACATCCA[C/T]GAGAATTACCTGCAG | 89910 |
rs370465245 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495942 | GCAGAGATTTTGTTT[A/T]TGGCCAGTTTTGGGG | 89910 |
rs370493351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539692 | GGGATCGAATTGACA[C/T]TCCTTCTGGAGTTTG | 89910 |
rs370576457 | snp | A/T | 3.30764e-05 | 0.00406659 | intron-variant | UBE3B | GRCh38.p7 | 12:109483827 | GCTACAAGCTGTTAA[A/T]TTAAAATGTCTTTTT | 89910 |
rs370585220 | snp | C/T | 3.62063e-05 | 0.00425463 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534791 | CTCCTAGCTCCTGTC[C/T]CAGCCCTGCCTCCAG | 89910 |
rs370590020 | snp | A/C | 2.11647e-05 | 0.00325298 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510435 | CCGGCGGCGCTTCAC[A/C]CCCGAGGACCACTGG | 89910 |
rs370593803 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109492088 | AACCACTCTGCCATT[A/G]CATCTTGAAAGCAGT | 89910 |
rs370725709 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109526387 | ACTGATTCCTGGAGG[A/G]AAGACCATTCCTGTT | 89910 |
rs370786061 | snp | C/G/T | 6.59352e-05 | 0.00574142 | intron-variant | UBE3B | GRCh38.p7 | 12:109503194 | AGATACTCACAGGTT[C/G/T]GCAGTCCCCAGGGCA | 89910 |
rs370821111 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488456 | ATTAAGACTGACTTA[C/T]AATCCTGACTCAGTG | 89910 |
rs370825092 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109530729 | CAGTTGATGTAATAA[C/T]TTACGCTGAAGAAAC | 89910 |
rs370825252 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510913 | TCAAGCTTTATGGCA[A/G]CTGCTGAAGCTGTGG | 89910 |
rs370834382 | snp | A/G | 8.25525e-05 | 0.00642413 | intron-variant | UBE3B | GRCh38.p7 | 12:109530522 | CGCTAGCACATTGCT[A/G]AGCCCAGGTCTGTAT | 89910 |
rs370843966 | snp | A/G | 6.97107e-05 | 0.00590343 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534732 | AAGAGCGTCCTCCGC[A/G]AGAAGCTGCGCTACG | 89910 |
rs370879008 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541789 | CTCTTCTAGCTTCTG[A/G]TGGCCCCTGCGTGCT | 89910 |
rs370887582 | in-del | -/GCCACTGGAGGTGCTG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513297 | TTCACGTGTGCTGTG[-/GCCACTGGAGGTGCTG]CACAATATTTTAAAT | 89910 |
rs370952056 | snp | C/G | 0.000252813 | 0.0112402 | intron-variant | UBE3B | GRCh38.p7 | 12:109511312 | CAAAAACGTGAGTTG[C/G]ACTCAGAGCTGGGCC | 89910 |
rs370955440 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487123 | TCTTACTCTGTCTTG[A/G]CTAAAGGGAGGAGAG | 89910 |
rs370965720 | snp | A/T | 9.88403e-05 | 0.00702925 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503163 | TCGCTGACAACTCTC[A/T]CACAGATTCGGCTGC | 89910 |
rs370992279 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478085 | ACTGGAGTTCGAATA[C/G]TGTTCGCTCGCTGTG | 89910 |
rs371000990 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496303 | TACCACATTTGAGTT[A/G]TTTCTACTTTTTGGC | 89910 |
rs371047200 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537298 | GGACACGCAGCCGTT[-/A]CTCACTGCATTCCCC | 89910 |
rs371072652 | snp | C/T | 3.33206e-05 | 0.00408156 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511214 | TCAAGGGATCTCAAA[C/T]CTAGCGTGCTCTTCC | 89910 |
rs371080492 | snp | C/T | 5.59289e-05 | 0.00528785 | intron-variant | UBE3B | GRCh38.p7 | 12:109511352 | CTTTCTATTCCCCCA[C/T]GTGGTTCCTGCCTTT | 89910 |
rs371384730 | snp | A/G | 1.65504e-05 | 0.00287662 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507721 | GTTCTGTGACTGTTC[A/G]CGGCACCTCATCACG | 89910 |
rs371386595 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109487960 | AGGCCTTTTGCTTGA[C/G]TTACACTTGGTGAAA | 89910 |
rs371397837 | snp | C/T | 0.000108984 | 0.00738106 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534809 | GCCCTGCCTCCAGGG[C/T]TCCTGGGCTGCCAGG | 89910 |
rs371427138 | snp | C/T | 3.31011e-05 | 0.0040681 | intron-variant | UBE3B | GRCh38.p7 | 12:109498213 | CAGTTTCTGATTTAA[C/T]GGTCTGCTATTCTTT | 89910 |
rs371457408 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516158 | AGGATTTTCTTTTTT[C/T]TTTTTTTTCTTTTTT | 89910 |
rs371469951 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510132 | ATGACACACTAGTGG[A/G]AGGCAGCATGAGTGA | 89910 |
rs371492874 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540300 | ACAACCTCCGCCTCC[A/G]AGGCTCAAGCAATCC | 89910 |
rs371503476 | snp | A/G | 1.65677e-05 | 0.00287812 | intron-variant | UBE3B | GRCh38.p7 | 12:109503238 | TCACATTTGGCAGAC[A/G]GTTTGTCTTAGCAAA | 89910 |
rs371521249 | snp | C/T | 6.59544e-05 | 0.0057422 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530648 | CGGATGAGAGAGCTA[C/T]GTTTCTGAAGGTATT | 89910 |
rs371552529 | snp | C/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109535084 | TAGTTTGATCTTTTG[C/G]GAGTCTGTCTTTCCT | 89910 |
rs371575065 | snp | A/G | 4.96504e-05 | 0.00498224 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516865 | CTCACATCACCATCC[A/G]CCGGTCCAGGATGCT | 89910 |
rs371590722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478839 | ACAAGTTGGTTAAAT[A/C]ATCTGTGCAGTGTCT | 89910 |
rs371614817 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480575 | AGAATCGCTTGAGCC[C/T]GGGAGGTAGAAGCTG | 89910 |
rs371629430 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109508938 | ATCGACTCTCAGTCA[A/G]TGTTCCTTGATATGC | 89910 |
rs371668886 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500890 | GGAACCACTAGGAGT[C/T]TCACCTCACCTTCTT | 89910 |
rs371710583 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537727 | GTTTTGTTTTTTTGA[A/G]ATGGAGTCTCGCTGT | 89910 |
rs371725562 | snp | A/T | 4.70179e-05 | 0.00484837 | intron-variant | UBE3B | GRCh38.p7 | 12:109510333 | GACTTTCCTGTTTGT[A/T]TGTCCCACAGAGAAC | 89910 |
rs371798394 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495075 | CCTGCAGAAAAGAAC[A/T]TGGTTCTCTTTTCAT | 89910 |
rs371809941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532809 | CCTCACTGGCTCTGG[A/G]GCCTCATTTTTGTCA | 89910 |
rs371910170 | snp | A/C | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535845 | CATTTCTCTTCCAAC[A/C]CATTGTGTTCCTCTG | 89910 |
rs371925079 | snp | C/T | 3.36842e-05 | 0.00410378 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534668 | AGGCGGCCGCCTGCC[C/T]ACCTCCTCCACCTGC | 89910 |
rs371984949 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | UBE3B | GRCh38.p7 | 12:109526479 | ATTCTGGCTCTCTGC[A/G]CTTATGTTGAGAATT | 89910 |
rs372028587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528289 | CTCTCTCCTTCCCTC[C/T]CTCTCACCTCCTCCC | 89910 |
rs372052099 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499747 | AGTATGTGTCTCAGA[A/G]GAAGTCCAACCTGAC | 89910 |
rs372115497 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484431 | AAGTCTCTCTCTGTC[A/G]CCAGGCTGGTGTGCA | 89910 |
rs372136566 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538902 | GGCACCTCACTGTGC[A/C]CCCTACACTGCACAT | 89910 |
rs372150461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109511726 | CTAGAGCAAGACAGC[C/T]TTAGAAACCAAGGCT | 89910 |
rs372221466 | snp | A/G | 0.000103001 | 0.00717564 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521513 | TACCTGCAGCTCTTC[A/G]AGTTTGTGGGGAAGA | 89910 |
rs372222827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475576 | GAGGGGTGGCTGATC[A/G]GTCACTAGTGTTTAA | 89910 |
rs372292606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109510627 | AAGCACCTGTCAGGA[C/T]GCTTCTGTTAAGAGA | 89910 |
rs372352298 | snp | A/G | 0.000115421 | 0.00759587 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498234 | GCTATTCTTTGCAGC[A/G]CCTCACTGTTTTAGA | 89910 |
rs372439376 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531069 | CTGTTCCTCCAGTAT[A/G]GAATTGTCAACTCTC | 89910 |
rs372494462 | snp | A/G | 1.65619e-05 | 0.00287762 | intron-variant | UBE3B | GRCh38.p7 | 12:109521107 | AATTGTGTGCATAAG[A/G]CTTTGGGCTTCCTAA | 89910 |
rs372569082 | in-del | -/CCCCC | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518291 | CCCCAGAAGAGGCCA[-/CCCCC]CCGCCACTCAGCTCC | 89910 |
rs372604916 | snp | A/G | 8.29745e-05 | 0.00644052 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483637 | TTGTGCAGAAGGAAC[A/G]GGAGCGGGCAGCTGT | 89910 |
rs372616845 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507619 | ATTTATCTGTGAGCT[C/T]GGGCCCCACGGAGGG | 89910 |
rs372644582 | snp | A/C | 0.000164853 | 0.00907741 | intron-variant | UBE3B | GRCh38.p7 | 12:109533440 | GGAGCCTGCCCCGTC[A/C]CCACTGACCCTGCTT | 89910 |
rs372661553 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523646 | GTGCTGGTACTGTGC[A/G]CGTTCCATCCTCTTA | 89910 |
rs372705093 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527700 | GCAGATTGGGAGGGA[C/T]TGCCTGCAAGAGTAG | 89910 |
rs372718403 | snp | C/G | 1.8267e-05 | 0.00302211 | intron-variant | UBE3B | GRCh38.p7 | 12:109490155 | CCTCTTCTTCCTTCC[C/G]CTGCCTTGTCTCACT | 89910 |
rs372728834 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533125 | CTGTTCCTCTTAACA[A/G]TCCCACAGGAGACCT | 89910 |
rs372744344 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484287 | ACAAATCATATTAAA[C/T]GGTAACTGACAGGCA | 89910 |
rs372750014 | snp | C/T | 3.3e-05 | 0.00406189 | intron-variant | UBE3B | GRCh38.p7 | 12:109503008 | TGCTCACATGTCTTC[C/T]TTTCTCCATGCCAGG | 89910 |
rs372759313 | snp | A/G | 3.30546e-05 | 0.00406524 | intron-variant | UBE3B | GRCh38.p7 | 12:109516748 | CTGTTTTCTGATCCC[A/G]CCTTTGTTCATTTTA | 89910 |
rs372773906 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538948 | GTGATTCAGAAGAAG[A/C]TGCATGGCCAGGCTC | 89910 |
rs372809787 | snp | A/C | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501462 | TGTGACATCCTGAGC[A/C]AGAAGCTACTGGAGA | 89910 |
rs372827099 | snp | A/G | 4.05836e-05 | 0.00450446 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510425 | AGCGGGACTGCCGGC[A/G]GCGCTTCACCCCCGA | 89910 |
rs372840694 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480789 | GCATGCTGTGGAAAA[C/T]TTAGAAAATACAGAC | 89910 |
rs372845836 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109492955 | AGCCGCATTTTTAAG[-/T]GCTCAGTAGCCACAT | 89910 |
rs372846302 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517110 | TGTCTTCCTTTACCC[A/C]ATGAGAGCTAGAGTA | 89910 |
rs373033803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485044 | TTACAGGCGTGAGCT[A/G]CCATCAATGTTCTAA | 89910 |
rs373048861 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503092 | CTGTCGGGGGTAAAC[A/G]GGTCGACTCTGCAGA | 89910 |
rs373077064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479421 | GGACATAGACACTAT[C/T]ATTACCCTCGATTTA | 89910 |
rs373127599 | snp | C/T | 6.76865e-05 | 0.0058171 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477248 | CTAGTCCATGGGCAC[C/T]GCCCTCCCTACCATG | 89910 |
rs373137217 | snp | A/C/T | 0.000163215 | 0.0090325 | intron-variant | UBE3B | GRCh38.p7 | 12:109486088 | TAAGTGGACGGGAGC[A/C/T]GCAGTGTCTCCCACA | 89910 |
rs373234197 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480843 | TTCAGTACCTCAAAA[-/C]CAGCCACTGGTAACA | 89910 |
rs373265333 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525060 | CCAAGGGCCGCTCAG[C/G]AGAAACCACGCCATG | 89910 |
rs373313874 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBE3B | GRCh38.p7 | 12:109526351 | TTACTCCCATCTTCT[C/T]CCCCAGCTTGTTTGC | 89910 |
rs373314734 | snp | A/G | 6.60415e-05 | 0.00574599 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511258 | GGACAGAAAACGGGC[A/G]CAGTTGATCCTGCAG | 89910 |
rs373316360 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539530 | CCCCTCAGACCTGCA[A/G]TTTCCTCTTCCATGA | 89910 |
rs373337503 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498339 | TAGAAGGATGCCATA[C/T]GCTTTGTCTAATGGG | 89910 |
rs373355311 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109514080 | CCTTAACATTTGTTA[A/C]AGCCTCAGCTCTGCC | 89910 |
rs373360499 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477068 | TCCCTACCACCACCC[A/C]CGCCCCTAATTCTCC | 89910 |
rs373366043 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109512293 | CGGAGTGAGAAGTCC[A/T]GGGCACTGAGGCAGA | 89910 |
rs373380833 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506417 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT | 89910 |
rs373439467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109541292 | CAGGCCGGTGACGGG[C/T]AATGTGGACTAGTGG | 89910 |
rs373512561 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109509407 | AGGTATTTGTCCTAA[A/G]GCTCTCCCTCCCCTT | 89910 |
rs373533946 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487165 | AGTTCAAAAATCCAG[A/G]TTTCTTGTAGGTCCA | 89910 |
rs373624920 | snp | A/G | 1.65597e-05 | 0.00287743 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509684 | TTCCTGAATTCTTTT[A/G]TGTTTAAGATGATCT | 89910 |
rs373625485 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500503 | TTTCTTTTGTTGTAC[C/T]TGAGTGACATCCCTG | 89910 |
rs373640919 | snp | A/G/T | 3.29679e-05 | 0.00405991 | intron-variant | UBE3B | GRCh38.p7 | 12:109489895 | GCAAGAGACTTTTTT[A/G/T]TTCTCACTGTTTTCT | 89910 |
rs373667919 | snp | C/T | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536055 | AAAGACGCAAAACAT[C/T]TTCCAACAAGAGCTG | 89910 |
rs373717944 | snp | A/C/T | 8.23627e-05 | 0.0064168 | synonymous-codon, stop-gained, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488593 | ATCCTGCAGGACTCC[A/C/T]GACTCATCACCCTGT | 89910 |
rs373859718 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477677 | GCGTCGGCTGCTGCC[C/T]CGGGTCTGGCAGAAC | 89910 |
rs373874193 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109522411 | AGAGTCCTGTTTCCC[A/T]GGAGGAAGGAAAGCT | 89910 |
rs373925222 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501223 | TGATTTGTTAGTTCC[A/G]CTTTTTATTTTTGTA | 89910 |
rs373926402 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3B | GRCh38.p7 | 12:109519640 | TGGAATTCTCCATCC[A/G]TTCTCATCTCAGTGC | 89910 |
rs374018902 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534420 | TCTCTGGAAGCCAGT[C/T]GTCTTGTGTCTGGGG | 89910 |
rs374025418 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480108 | GGAAAAAAGTTAATG[A/G]GTGAGAAATGTCAGA | 89910 |
rs374025917 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502714 | CTAATATAGTCCTCT[A/G]AATTTTTACCATTGT | 89910 |
rs374032767 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497673 | TGTCCATTTCCCCAG[G/T]GTATGTCCCCAATTT | 89910 |
rs374046452 | snp | A/G | 5.05412e-05 | 0.00502673 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534657 | AAGCGGGAGCCAGGC[A/G]GCCGCCTGCCCACCT | 89910 |
rs374082823 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516167 | TTTTTTCTTTTTTTT[-/C]TTTTTTTTTTTTTTT | 89910 |
rs374117870 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499646 | AGGCAACCTCCTACA[C/T]TTGGGCTCCCTCAGC | 89910 |
rs374127222 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109529956 | AAACCAAACAGCTGC[C/T]CTCATTAGCGGATTC | 89910 |
rs374132856 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515379 | TTTGTTGTTGTTGTT[A/G]TTGTTTTGAGACAGA | 89910 |
rs374191030 | snp | A/G | 1.77767e-05 | 0.00298128 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534750 | AAGCTGCGCTACGCC[A/G]TCAGCATGAACACGG | 89910 |
rs374215887 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488872 | GTGTTGTACTCAACC[C/T]TTCTTTGAATTTACA | 89910 |
rs374216396 | snp | C/T | 5.07172e-05 | 0.00503548 | intron-variant | UBE3B | GRCh38.p7 | 12:109501561 | GAGCAGGCCCAACCC[C/T]GTAGCTCCACTTGGC | 89910 |
rs374242166 | snp | C/T | 1.76424e-05 | 0.00297 | intron-variant | UBE3B | GRCh38.p7 | 12:109499852 | TTTCCTGCCTCTCTC[C/T]CACCATCTTCTTCTT | 89910 |
rs374246772 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537731 | TGTTTTTTTGAGATG[A/G]AGTCTCGCTGTCGCC | 89910 |
rs374276396 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514962 | TCTGTCGCCCAGGCT[A/G]GAGTGCAGTGGCGCG | 89910 |
rs374346591 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526426 | AAATAAGTGAGTATA[A/G]CAATTAGGTTTTTAA | 89910 |
rs374348924 | snp | C/T | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503172 | ACTCTCACACAGATT[C/T]GGCTGCAGATACTCA | 89910 |
rs374374638 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535259 | CCTCGCCAAGCCTCT[A/G]TGCACCCCACAAAGT | 89910 |
rs374406550 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487716 | CAAACAAAAAAAGTT[C/T]ATGCAAAGAAACAGA | 89910 |
rs374427871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109511544 | ACGGAGACCTGACCA[G/T]CTGGAGGGAGGGAAA | 89910 |
rs374684265 | snp | A/C/G | 0.0001489 | 0.00862738 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524492 | TCTTACGACGAGGAC[A/C/G]TCATGGGTCAGGTAG | 89910 |
rs374713884 | in-del | -/TGGCCACTGGAGGTGC | 0.0162398 | 0.0886349 | intron-variant | UBE3B | GRCh38.p7 | 12:109513295 | GGTTCACGTGTGCTG[-/TGGCCACTGGAGGTGC]TGCACAATATTTTAA | 89910 |
rs374718999 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516167 | TTTTTTCTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 89910 |
rs374744734 | snp | A/G | 3.31225e-05 | 0.00406941 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516868 | ACATCACCATCCGCC[A/G]GTCCAGGATGCTGGA | 89910 |
rs374747896 | snp | A/G | 4.96348e-05 | 0.00498146 | intron-variant | UBE3B | GRCh38.p7 | 12:109530496 | CCTGCCTGCCTGTCC[A/G]TAAGTGCCCACGCTA | 89910 |
rs374753771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486793 | CACGCCACAGCCTCC[A/G]TGGCAGGGAATCTGT | 89910 |
rs374772085 | in-del | -/TT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527436 | GGAGCATCAGTCTCT[-/TT]AGTGACAAGTGAGGG | 89910 |
rs374804291 | snp | C/G | 6.86401e-05 | 0.00585793 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521509 | GAATTACCTGCAGCT[C/G]TTCGAGTTTGTGGGG | 89910 |
rs374891002 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109494180 | GAAGTTAAACTGTTT[G/T]CTCTTGGTCACACAG | 89910 |
rs374991203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533240 | CAGTCGCACCTATTG[A/G]GTATGGGTTTCATGT | 89910 |
rs375032042 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524073 | GGTGGATGAACTGCC[C/T]TCTCTGGACTCCGAG | 89910 |
rs375050551 | snp | A/G/T | 0.000131866 | 0.00811894 | intron-variant | UBE3B | GRCh38.p7 | 12:109497948 | CTCTGTGAGTTCCCC[A/G/T]TGAAAACCCAATTGT | 89910 |
rs375062055 | snp | C/T | 6.59087e-05 | 0.00574021 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521310 | GTTTTTGACCCAGCA[C/T]TCAATCTGTTCAAGG | 89910 |
rs375063722 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495540 | AGAGGAATTAAAGAC[A/C]CACACACAGAAATAT | 89910 |
rs375089150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527204 | AGACTCTGAGGCCCA[A/G]CAACTATTGTCACAG | 89910 |
rs375093429 | snp | A/C | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488656 | TCAACGTGGAAAATT[A/C]TTCGGGGAAAAGGTC | 89910 |
rs375121190 | snp | A/G | | | intron-variant, missense | UBE3B | GRCh38.p7 | 12:109533957 | CAGCAGGCTGTGCAC[A/G]TCCAGGCTCGCTGCT | 89910 |
rs375131150 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523303 | GTCTGCCTCCTGTCT[G/T]CCTCTCGCCAGCCCA | 89910 |
rs375134911 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537820 | CACCATTCTCCTGCC[A/G]CAGCCTCCCACATAG | 89910 |
rs375154171 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109512185 | AAATCTCCTGACTGC[C/T]CCCATGGACTGGGTG | 89910 |
rs375156821 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532959 | AATAAGGAGCCGGCA[A/G]GATGCCAAGTGCAAG | 89910 |
rs375186905 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518999 | ATTGTTTCCTTTTTT[-/T]ATGGTTAGTATTGAG | 89910 |
rs375191730 | snp | A/T | 1.65831e-05 | 0.00287945 | intron-variant | UBE3B | GRCh38.p7 | 12:109523948 | TCAGAATCCTGGCTG[A/T]TGGACAGCTCTGCTT | 89910 |
rs375217782 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501657 | GTTTTTGTTGTTATC[A/G]TTCTTGTTGTTAGAG | 89910 |
rs375236597 | snp | A/G | 0.000181194 | 0.00951651 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497846 | GCACAGTTCTCAGAC[A/G]ATCTGATTCGGCCGT | 89910 |
rs375274454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491199 | GGTTTTTCTTTCTCT[C/G]GTTACTGGTATTAGG | 89910 |
rs375289269 | in-del | -/CCATGGGTGTTCC | 0.0788843 | 0.182262 | intron-variant | UBE3B | GRCh38.p7 | 12:109524333 | CAAGCTGTTCAGCAG[-/CCATGGGTGTTCC]CAGCACCAAAGCAGC | 89910 |
rs375298625 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539745 | GCTTTGGCTGACGTT[A/G]ACAGGACATCCCGGG | 89910 |
rs375335935 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109533411 | CAGCTGCAAGGGCCC[A/G]TCCTGGAAGAGCAGG | 89910 |
rs375384123 | snp | C/G/T | 5.93928e-05 | 0.00544917 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510412 | ATGGTGCTGTACGAG[C/G/T]GGGACTGCCGGCGGC | 89910 |
rs375548041 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484115 | TGTCCCTTTTGTTTT[A/C/T]TTGGGACCTGTTTTG | 89910 |
rs375625631 | snp | C/T | 0.000119088 | 0.00771556 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477289 | GGACGCAGGAGTCTC[C/T]AAACCCGGACTGAGA | 89910 |
rs375632180 | snp | A/G | 9.95933e-05 | 0.00705597 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483638 | TGTGCAGAAGGAACG[A/G]GAGCGGGCAGCTGTT | 89910 |
rs375635592 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510437 | GGCGGCGCTTCACCC[C/T]CGAGGACCACTGGCT | 89910 |
rs375643683 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE3B | GRCh38.p7 | 12:109483286 | CCAGGTGCTGTGCTC[C/T]TTCCCTTAAGAAGAT | 89910 |
rs375692065 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109499413 | ATGGGTTGACGGCCA[C/T]GGCTCACCTTGTCTG | 89910 |
rs375692389 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487383 | GAGGCTTGGCAAGGA[C/T]ACAGATAGCAGCTCA | 89910 |
rs375736666 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506433 | GGCTCACTGCAACCT[C/T]TGCCTCCCAGGTTCA | 89910 |
rs375737107 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525596 | TGGCTTCAAATGATA[C/T]GTCCTTTGATTTTTA | 89910 |
rs375756386 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109509358 | TTGCTGCACCTGTCA[-/C]CCCGTCATCTAGGTT | 89910 |
rs375781261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517370 | ACAGAAACTTACAAG[A/T]TACCACTGAAGTGAC | 89910 |
rs375876329 | snp | A/C | 1.64923e-05 | 0.00287156 | intron-variant | UBE3B | GRCh38.p7 | 12:109533419 | AGGGCCCGTCCTGGA[A/C]GAGCAGGAGCCTGCC | 89910 |
rs375969272 | in-del | -/T | 0.0967024 | 0.197484 | intron-variant | UBE3B | GRCh38.p7 | 12:109513690 | ATAGTAATCCCCACA[-/T]TTTTTTTTTCTTTTG | 89910 |
rs376000542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507904 | AGTGTGCAGTAAATG[C/T]TCAGCAGTTGTTAGG | 89910 |
rs376000909 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480843 | TTTCAGTACCTCAAA[A/C]CAGCCACTGGTAACA | 89910 |
rs376005630 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109527653 | CTCCTTGGCCACAGG[A/G]CATTAGTTTGAAAAC | 89910 |
rs376035800 | snp | G/T | 3.31312e-05 | 0.00406995 | intron-variant | UBE3B | GRCh38.p7 | 12:109530102 | GGGGGAAGGGTGAAA[G/T]TCCTTGGCCTCCCAG | 89910 |
rs376040921 | snp | C/T | 0.000108527 | 0.00736556 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534787 | AACTCTCCTAGCTCC[C/T]GTCCCAGCCCTGCCT | 89910 |
rs376149192 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109530797 | CTCTCCCACAGGCAG[A/G]CCTCCCGGTAGGCCA | 89910 |
rs376162558 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510011 | CTTCCATTTGATTTC[C/T]GTGAAGATAAAACAT | 89910 |
rs376167553 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489291 | ATAATGTGGTAAGTG[C/T]TTGGAAGGAAGCATG | 89910 |
rs376210471 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504973 | ACCATGCCCGGCTAA[-/T]TTTTTTTTTTGTATT | 89910 |
rs376213401 | snp | A/C/G | 3.30241e-05 | 0.0040634 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511254 | ACAGGGACAGAAAAC[A/C/G]GGCACAGTTGATCCT | 89910 |
rs376232986 | snp | C/T | 0.00018185 | 0.00953372 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511278 | TGATCCTGCAGTACA[C/T]CCCACATGTCATCCC | 89910 |
rs376242194 | snp | C/T | 0.000109587 | 0.00740145 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534831 | GCTGCCAGGGACCTT[C/T]AGCTCCCAGAGGCAG | 89910 |
rs376253129 | snp | A/C | | | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534146 | GAGCCCGTGATGCCA[A/C]CTTGTACAGGAAGCT | 89910 |
rs376259551 | snp | C/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477250 | AGTCCATGGGCACCG[C/T]CCTCCCTACCATGAA | 89910 |
rs376394269 | snp | C/G | 0.000319782 | 0.0126408 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534671 | CGGCCGCCTGCCCAC[C/G]TCCTCCACCTGCTTC | 89910 |
rs376407012 | in-del | -/ACAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504583 | TGTGTTGTGGCTGTG[-/ACAA]GGGAAAGGGGCCTGC | 89910 |
rs376481440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109525105 | GAGCCGACTTATTAG[A/G]CTCGCGCTTGGGCAC | 89910 |
rs376485678 | in-del | -/T | 0.494358 | 0.0528145 | intron-variant | UBE3B | GRCh38.p7 | 12:109520744 | GTTCTGTAGGTTTGA[-/T]TTTTTTTTTTTTTCT | 89910 |
rs376501677 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518479 | CCACCCATTTGCAAC[C/T]TCTGCTTTTGATTCA | 89910 |
rs376517537 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503110 | TCGACTCTGCAGAAG[C/T]CCAGAAGGTTTGCAA | 89910 |
rs376526924 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540886 | AGACCAGCTCAGAGC[C/T]AGAGCAGGTGGTGAG | 89910 |
rs376669302 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538649 | CCATGACCCTGGAGA[G/T]CAGGCTCGGATTAAG | 89910 |
rs376690658 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488598 | GCAGGACTCCCGACT[C/T]ATCACCCTGTACCTC | 89910 |
rs376714335 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524724 | TTCCCGCAGAGACCC[A/T]GCTTTCTTATATCGC | 89910 |
rs376743176 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478586 | AGAAGTTCAAGACCA[A/G]CGTGGCCAACATGGT | 89910 |
rs376752676 | snp | C/T | 3.37439e-05 | 0.00410741 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483683 | TGTCCGGAGTTTTCT[C/T]TGTCGGAGTCGACTG | 89910 |
rs376756684 | snp | A/G | 7.66665e-05 | 0.00619091 | intron-variant | UBE3B | GRCh38.p7 | 12:109521596 | AAATAAAATGTTAAC[A/G]GTACCATGGGCTTCT | 89910 |
rs376773160 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109499423 | GGCCACGGCTCACCT[C/T]GTCTGTGGCATAGCC | 89910 |
rs376853832 | snp | A/G | 1.69911e-05 | 0.00291466 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534615 | GACACTCTGGGCAGC[A/G]TCCTCCGGGGCTTCT | 89910 |
rs376885266 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | UBE3B | GRCh38.p7 | 12:109510294 | GCTGTCCTCCCCTTG[C/T]TCTCTGGCTCTGACT | 89910 |
rs376922633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109529702 | ATGTGCACACAGTGG[C/T]GTATGGTGTGCAGTT | 89910 |
rs376987184 | snp | G/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503033 | GCCAGGTCTCCTAAA[G/T]CGTGCTTTTCAAAAG | 89910 |
rs377095229 | snp | G/T | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507677 | AATGACACTGAAGAG[G/T]CCAAGCAACTCTTGG | 89910 |
rs377115151 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506763 | GATGCCTCCATATTT[G/T]GAGTCCTTAAGTAAG | 89910 |
rs377310864 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE3B | GRCh38.p7 | 12:109484017 | ATGTATAATACTTCC[A/G]TATGTCAGATCTTTT | 89910 |
rs377311046 | in-del | -/GAT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497459 | CCCAATAGAGAAATC[-/GAT]TATACCAGCACTCCA | 89910 |
rs377311592 | snp | C/T | 1.65072e-05 | 0.00287286 | intron-variant | UBE3B | GRCh38.p7 | 12:109516759 | TCCCGCCTTTGTTCA[C/T]TTTAGAGAGTTCTAC | 89910 |
rs377311778 | snp | C/T | | | utr-variant-3-prime, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490697 | CTGTTTTTTTAACTT[C/T]ATTATTAAAGAATTT | 89910 |
rs377327621 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532033 | GTGACCACGACCATG[C/G]TTCTCTTAAATGTAA | 89910 |
rs377343817 | snp | A/G | 1.648e-05 | 0.0028705 | intron-variant | UBE3B | GRCh38.p7 | 12:109526419 | CAAATGAAAATAAGT[A/G]AGTATAGCAATTAGG | 89910 |
rs377353860 | snp | A/T | 0.000437904 | 0.0147905 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477331 | CACCCAGCTCACGCC[A/T]GCCGGGGGCGGAGGC | 89910 |
rs377395669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109481877 | TAAAAAAGTTGAAAC[C/T]CACAATTACTTTTGT | 89910 |
rs377434699 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479687 | AGGAAAGGATGAGAA[A/G]AACTGTAAAGTGTAG | 89910 |
rs377446075 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515115 | AGACGGGGTTTCACC[C/G]TGTTAGCCAGGATGG | 89910 |
rs377462796 | snp | C/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486567 | TGTGATTTTCTCAAG[C/G]AGCTCAAGGTAACAA | 89910 |
rs377488686 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504951 | GCTGGGATTACAGGC[A/G]CCTGCCACCATGCCC | 89910 |
rs377548629 | snp | A/G | 4.94344e-05 | 0.00497139 | intron-variant | UBE3B | GRCh38.p7 | 12:109488692 | GACTTGCTTCAAAAT[A/G]TTCTCTAACCAACAT | 89910 |
rs377553465 | snp | C/T | 1.74027e-05 | 0.00294975 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521446 | TGCCTTGCAGACAAC[C/T]AGTGGGGATGAGAGG | 89910 |
rs377597031 | in-del | -/T | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109482705 | AGTGCTGTGTGCTTT[-/T]AGGCTGCTAGCAAAA | 89910 |
rs377622854 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBE3B | GRCh38.p7 | 12:109501566 | GGCCCAACCCTGTAG[C/T]TCCACTTGGCTGAAG | 89910 |
rs377630367 | snp | A/G | 0.000753296 | 0.0193928 | intron-variant | UBE3B | GRCh38.p7 | 12:109533829 | GGGTGGGTACGTGCT[A/G]TTTTTAGTGGCGTCT | 89910 |
rs377638294 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513840 | GGGGGAGTATCTAAG[A/G]CTTGGTGTTTTCAGA | 89910 |
rs377643944 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496350 | GCTGTGAACATTTAT[A/G]TACAAGTTTTTGTAT | 89910 |
rs377657901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109519190 | TGAGGCCAGAGAACT[G/T]CAGTCAAGGTCACTT | 89910 |
rs377676632 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536432 | AAGGTTGGAACCAGT[A/G]AGGGACTGGGAGAGA | 89910 |
rs386377730 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480657 | CCTGCCTTAAAAAAA[-/A]AAAAAAAGACTTAGA | 89910 |
rs386377731 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513693 | TAATCCCCACATTTT[-/T]TTTTTTCTTTTGGGA | 89910 |
rs386766303 | multinucleotide-polymorphism | AAA/GAG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527852 | GTGTCAGGCTCAGAG[AAA/GAG]GGCTTAAATGACAGC | 89910 |
rs397714137 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109543381 | GCACGGGGTCAGCGG[-/G]CTGGTAACACAGCAG | 89910 |
rs398021030 | in-del | -/T | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109504821 | CTTTTTTTTTTTTTT[-/T]CGAGACGGAGTCTCA | 89910 |
rs398021031 | in-del | -/TT | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109520756 | TGATTTTTTTTTTTT[-/TT]CTTTTTTCTTTTTTT | 89910 |
rs398021032 | in-del | -/A | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109521588 | GAAATGTAAAATAAA[-/A]TGTTAACGGTACCAT | 89910 |
rs398044809 | in-del | -/T | 0.5 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109516169 | TTTTCTTTTTTTTCT[-/T]TTTTTTTTTTTTTTT | 89910 |
rs398098498 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515366 | TTATTACTGTTTTTT[-/T]GTTGTTGTTGTTGTT | 89910 |
rs398123020 | snp | C/T | | | splice-donor-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509716 | GGATGGAATTGTAGG[C/T]AAGAGAAAAGGTGTC | 89910 |
rs398123021 | in-del | -/AG | | | frameshift-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521294 | AGAGATCATCAAGAG[-/AG]TTTTTGACCCAGCAC | 89910 |
rs398123022 | snp | A/G | | | splice-acceptor-variant | UBE3B | GRCh38.p7 | 12:109489917 | CTGTTTTCTTTCTTT[A/G]GGTGAAAGTCTTCGA | 89910 |
rs398123023 | snp | A/C | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521251 | AAGCAGGGATTGATC[A/C]AGACGGTGTTTTTAA | 89910 |
rs527374076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109506408 | GGCTAGAGTGCAGTG[A/G]TGCGATCTCGGCTCA | 89910 |
rs527418518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513344 | TCTGAGGAGAACACA[A/G]TGAGACACCACATGA | 89910 |
rs527458018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486715 | TTCTGGAAGAGAGGA[A/G]TTTTGATTCTGTTAT | 89910 |
rs527519613 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109493699 | GAAAGTCTATAAAAT[A/C/T]GTCAGTGGTGTGCCA | 89910 |
rs527569370 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533299 | AGAGAGATGTACGGC[A/G]TGTGCCAGTTTTGGG | 89910 |
rs527574666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538924 | ACTGCACATACAATC[C/G]CTTGGACTGTGATTC | 89910 |
rs527581722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533057 | GCCTCGCCCTCACCG[A/T]CTCCCATTTTCTCCT | 89910 |
rs527596645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499408 | GAGACATGGGTTGAC[A/G]GCCACGGCTCACCTT | 89910 |
rs527667160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484727 | TAAAGAGATGCCAAA[C/G]ATCTGAGTTTTTATG | 89910 |
rs527695622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536776 | TCTGGGCTTAGGGAG[A/C]ATGTAGGCTTCCACA | 89910 |
rs527727945 | snp | A/C | 1.65422e-05 | 0.0028759 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491164 | AGGTGTTGGCATGTT[A/C]TTGAATGCTTCCTCC | 89910 |
rs527801321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505510 | TCCACAGTGTTAACT[A/G]TTTCCTCTGTTTCTA | 89910 |
rs527812204 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109542879 | TATGGTGCTTTGTTC[C/T]GTCAGCCACAGGAAA | 89910 |
rs527843275 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | UBE3B | GRCh38.p7 | 12:109520542 | TGATCCCTGCCATCC[A/C]CCTGCTCTGCTGCCA | 89910 |
rs527974430 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500045 | CTATCTAGAAATACT[A/G]ATCCTTTTTTACAAA | 89910 |
rs527988647 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109526612 | GCACAGTGGCTCATG[A/C]CTATAATCCCAGCAC | 89910 |
rs528050259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518209 | GAAAAATAGCCCCCA[C/T]GAGTGAGTTGATAAA | 89910 |
rs528073214 | snp | C/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535439 | CCCTCCCATTTTCTG[C/G]GTCCTCAGCGGGCTG | 89910 |
rs528095531 | snp | A/C | 6.85389e-05 | 0.00585361 | intron-variant | UBE3B | GRCh38.p7 | 12:109483725 | CAGGTAAGGGCTAGG[A/C]TCTCCCTAGCACATG | 89910 |
rs528121017 | snp | A/G | | | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543907 | AAGGAGGGTTGGAGC[A/G]GGCCTCTCAAAGCAA | 89910 |
rs528169730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109524907 | GCATACAGAGCAGAG[C/T]AGGGAGCAGAGACCC | 89910 |
rs528171156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109530894 | AGGCCCCCTGCACAG[A/G]TGGGCATACCTGTTG | 89910 |
rs528208828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109530495 | ACCTGCCTGCCTGTC[C/G]ATAAGTGCCCACGCT | 89910 |
rs528256818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542521 | CATCCTAACCCCCAC[A/T]ACCTCAGCATGTGGC | 89910 |
rs528360564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109511439 | GAAACGGTGGTTGCT[A/G]TTACTTTGGTGAGGT | 89910 |
rs528386447 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109519281 | CTGTGTGTGCATGTT[A/G]AGATGCAGTGAAGAA | 89910 |
rs528397628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518917 | AATATGAGAGCCCAG[A/G]GGCCTTTGCTGGATT | 89910 |
rs528440126 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109515456 | CTCACCACAACCTGC[A/G]CCTCCCAAGTTCAAG | 89910 |
rs528478288 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518128 | GCTAGACATATAGAA[A/G]TAATCTCCACTTCTG | 89910 |
rs528494779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510087 | CCAATTGCTCAGGAC[A/G]AAGCTCCTTAGACTT | 89910 |
rs528561564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517085 | GTTCTCATTGCTGGA[A/G]ACCCAGCAGTGTCTT | 89910 |
rs528607845 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109516442 | TGGGCCTCCCAGAGT[G/T]CTGGGATTACAGGCG | 89910 |
rs528651441 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535747 | GTCTTGCTGCCCATC[C/T]TTCCTCAGCACAGGG | 89910 |
rs528713420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109503690 | TATCTCATCACATGG[A/T]TATGCCCAACATTTT | 89910 |
rs528723092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496486 | CAGAGTGCCTGTGCT[A/G]TTTTACCTTCCCAGG | 89910 |
rs528730297 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537992 | AGGCGTGAGCCACCG[C/T]GCCCGGCCAACATTC | 89910 |
rs528738484 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109495920 | ATCACGAACATGTCA[C/T]AATGCTGCAGAGATT | 89910 |
rs528776713 | snp | C/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503063 | GTCGGCATCAGTCCG[C/G]AATATTCTCAGGCCT | 89910 |
rs528854156 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481176 | CCCAACTGAGATAGG[A/G]TATGGTGGCACACAC | 89910 |
rs528890210 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515974 | AGGGAGCTTTATACT[A/G]TAGGGTCATTTTTAA | 89910 |
rs528922508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109511543 | TACGGAGACCTGACC[A/G]GCTGGAGGGAGGGAA | 89910 |
rs528932198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518948 | TGGACACAAGGGGGC[A/G]TCAGTAAGCTGATCT | 89910 |
rs528968927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109525378 | AAGAATGCTGTCTCG[C/T]AGGATCGTTCTCTAC | 89910 |
rs529018629 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543654 | CCTGGCCAACATGGC[A/G]AAACCTCGTCTCTAC | 89910 |
rs529018925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536887 | TATTTGCTTCCAATT[A/G]TGTTTCAAGAAGTAA | 89910 |
rs529056617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109543125 | TCTCCAGATTTAAAA[A/G]TTGTTGGCAGATTGA | 89910 |
rs529087157 | snp | C/T | 1.66214e-05 | 0.00288278 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491179 | CTTGAATGCTTCCTC[C/T]TCTTGGTTTTTCTTT | 89910 |
rs529135439 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109506069 | CCTTGTAGCCATCAG[A/G]AAACAAATTTAGAAA | 89910 |
rs529136813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505597 | CATGGACAGTTGAAA[A/G]ACTAGTTATGAGTGG | 89910 |
rs529177572 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483283 | ATGCCAGGTGCTGTG[C/T]TCTTTCCCTTAAGAA | 89910 |
rs529268725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109541560 | CCAGGCAGGGTGGAG[C/T]ATTGGGTCAGAAGGT | 89910 |
rs529309783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109503280 | TTTTCTGGCTTCTTT[A/G]ACTCTGAAAATAGAT | 89910 |
rs529318790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504004 | AAAGAGAGAGCCAAG[G/T]TCTTCGTTCTCAAGG | 89910 |
rs529330722 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109510578 | TGCTTCATTTTGTCT[A/C/G]TTCATTTGTGTAAAG | 89910 |
rs529334996 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109507437 | TTCTCCATAATCCCA[-/C]CTTCTTTTCACGCAC | 89910 |
rs529380088 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536347 | ACGCTGGGCGGGTTC[A/G]TGCATACATGCGGGG | 89910 |
rs529405856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517878 | CTTCATTTTCTCCCT[C/T]GGTGCATCGTACCTT | 89910 |
rs529413628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510162 | ATTTTGTCTGAGAGG[C/T]ACTCAGGCCCTGCAG | 89910 |
rs529418891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534441 | GTGTCTGGGGCTTGA[A/C]CTCGGGTAGTGGTGC | 89910 |
rs529443721 | snp | C/T | 3.30513e-05 | 0.00406504 | intron-variant | UBE3B | GRCh38.p7 | 12:109483840 | AATTTAAAATGTCTT[C/T]TTTTGCACTTTCTTT | 89910 |
rs529496924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497310 | ATACTTATATATAGT[A/G]TACATACTATAGATA | 89910 |
rs529517375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109489785 | TCTGGCACCAGGCCT[A/G]AGGGAAAAGGGAGGC | 89910 |
rs529584441 | snp | C/G | 1.64735e-05 | 0.00286993 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109530604 | AGTCATCATCTGGCT[C/G]TGGGATATTCTGGCC | 89910 |
rs529595881 | in-del | -/TCTA | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109526074 | ATTTAACCGTCCTAC[-/TCTA]TCTACTCCGAAATGC | 89910 |
rs529617500 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535823 | TTTTTGTTTTTTTTT[A/T]AAACTTCATTTCTCT | 89910 |
rs529664266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109529244 | CTGTTGAGAGGATTA[C/T]ATGCTTTATGCAGTT | 89910 |
rs529728419 | in-del | -/AG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525427 | GGTGTTCCTGGAATC[-/AG]GGGAAACCTCAGGCT | 89910 |
rs529784491 | snp | A/G/T | 7.28616e-05 | 0.00603541 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534541 | TTGGCATCAGCCTGG[A/G/T]CTCCCAAACTAGGCC | 89910 |
rs529827606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109501983 | GCTTGTTCCACAACA[A/G]TTTTGAGGCTTGTTA | 89910 |
rs529914939 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109482341 | TGTCCCATCTCCCAC[C/G]TTTTGGAGTCTCCAT | 89910 |
rs529954423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517117 | CTTTACCCCATGAGA[G/T]CTAGAGTATCCTGGG | 89910 |
rs529959283 | snp | A/G | 6.62372e-05 | 0.0057545 | intron-variant | UBE3B | GRCh38.p7 | 12:109529847 | GTGACAGCCTGCCCC[A/G]TCCTGTTAATTGTCA | 89910 |
rs529998058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522812 | GATTTGGGTCCTGGG[C/T]CCATTCTCTGTGCCT | 89910 |
rs530122740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109480470 | AACCTGGGCAATATA[A/G]CGAGACCCCACCTCT | 89910 |
rs530147848 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109527780 | CCTGCCATGTAACCT[A/G]TAGCCATTCCTTTAG | 89910 |
rs530187251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479481 | TAAGTAACTTGGCCA[A/G]ATGTCGGATAGAAGG | 89910 |
rs530202194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539484 | CAGCTCTGCCGCCCA[C/T]GATCTGGGAGGCCGG | 89910 |
rs530282311 | snp | C/T | | | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543690 | ACACAAAAATTAGCC[C/T]GGCATGGTGGCAGGC | 89910 |
rs530319267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109488260 | CTGTTGCTGCAGAGT[G/T]CAGACAGACAGGCAG | 89910 |
rs530393916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109541997 | AAAAGGTCCCATGCA[C/T]AGGTTCTGGGGGTTA | 89910 |
rs530513454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482906 | CATAAAACCAAATAT[C/T]TTCAATATAATGGAC | 89910 |
rs530533238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109489613 | CGAAGGCAGTGCTAG[G/T]CCCTAGGAGGGAATT | 89910 |
rs530591049 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488615 | TCACCCTGTACCTCA[C/T]GATGCTTGTCACCTT | 89910 |
rs530625803 | snp | A/G | 8.23621e-05 | 0.00641672 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530027 | CTCCTGAACTGCAGC[A/G]TCTCATCTCTGGCGA | 89910 |
rs530732524 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109524852 | TGCCACCTGAGAAGC[A/G]CCTCAAGCTCAAGCA | 89910 |
rs530746485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475589 | TCAGTCACTAGTGTT[C/T]AAAAAGCTCTTTGGG | 89910 |
rs530769459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518809 | TCTTAGGCTTTAGGC[A/G]AAGTCCCTTTTCCTC | 89910 |
rs530793871 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109537819 | ACACCATTCTCCTGC[C/T]GCAGCCTCCCACATA | 89910 |
rs530822990 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109490398 | GATCATACCTCTAGG[A/G]AATTGTTGAGAAAGC | 89910 |
rs530842231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109508860 | TGCTTACTAAGTACC[G/T]GCTAAGTGTCACTAG | 89910 |
rs530846557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109517169 | GTCCCTTTGAAATGA[A/G]GACAGGAGCTGCCAG | 89910 |
rs530855275 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109516420 | GACCTCAGGTAATCC[A/G]CCCACCTGGGCCTCC | 89910 |
rs530877799 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529402 | CCGCCTTGCCATAGC[A/G]TTAGACTGTTGATCC | 89910 |
rs530886787 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109523630 | CCCTGAGAGCTTGGG[A/G]GTGCTGGTACTGTGC | 89910 |
rs530893114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515589 | GGTCAGGCTGGTCTC[A/G]AACTCCCGACCTCAG | 89910 |
rs530940752 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109481669 | TCTGAAGTGAGAAGC[G/T]GTTCTCAGCCACGAG | 89910 |
rs531001996 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512743 | CTTTCCCCCTCAAGC[A/C]GTGATGTGCAAACAA | 89910 |
rs531018228 | in-del | -/CTC | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541685 | CAACGGAAATGTATT[-/CTC]CTCGGACAGTTCTGG | 89910 |
rs531020774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109539876 | TCCTCCACCCGGGGA[C/T]CAGCAGTTGCAGTTC | 89910 |
rs531068185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510058 | GAGATGAGAGTCCAC[C/G]TCCCGAAGTGTCTCC | 89910 |
rs531102973 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540327 | ATCCTCCCACCTCAG[C/T]CTCCCAGGTAGCTGG | 89910 |
rs531297990 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109538999 | TGAACACTTTGGGAG[A/G]CTGAGGCGGGCAGAT | 89910 |
rs531327525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507100 | TAATTTAACAGCAGA[A/G]ACCTTCTGGCCCACA | 89910 |
rs531371066 | in-del | -/CGT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109530921 | TTGTGCTCGGCACTC[-/CGT]CGTCCTCCCCTTTGC | 89910 |
rs531396957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507792 | TGGAGAGACCAAAAT[A/G]CAGTGTCAGTAAGGA | 89910 |
rs531409954 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109500968 | GCAGTGTGGAGTCAG[A/G/T]CAAGGAACCCCTGGA | 89910 |
rs531412083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109479634 | GTTTTATTAATTGAC[A/G]AACTATAGTATACAC | 89910 |
rs531414421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487200 | ATCCTGGGTTCATCT[C/T]TGAACCAGTCACAGT | 89910 |
rs531487499 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109528488 | AGCATTGTAAAACAT[C/T]TATTTGGACTCTACT | 89910 |
rs531499189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527909 | GGTGACGTGTCACAT[A/G]GATCCTGCCACCCCC | 89910 |
rs531604391 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478016 | AATGCTGGGTGATTT[G/T]TTCCTGTGGTTGTTG | 89910 |
rs531687391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532907 | ATCAGCAGGCCCAGG[A/G]CTCAGGTGACTGCAC | 89910 |
rs531812488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109491908 | CAAACGTATCTGAGC[A/G]TGGAATACCCCTGCC | 89910 |
rs531961066 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109487290 | TCAGTGTTCTGAAAA[A/G]GATGGACAGGGGTGT | 89910 |
rs531983115 | snp | A/G | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109514257 | GCTTTGTAGTATGGG[A/G]GCTGTGTCTGGGCTT | 89910 |
rs532049562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527150 | ACCGTGATGAATTCA[A/G]ATGCCACAGACGGAG | 89910 |
rs532059916 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496784 | CTCTAGATACAAGTC[C/T]CTTTTCAGACAAGTG | 89910 |
rs532065756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478583 | GTCAGAAGTTCAAGA[C/G]CAGCGTGGCCAACAT | 89910 |
rs532127059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109500569 | ACAGCCTGCCCCAGC[A/G]TGACACCTCAGCCTG | 89910 |
rs532140729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539453 | CTCAGAGCATCCTGC[C/T]GCTGGGTGCAAACCC | 89910 |
rs532175040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494366 | TCCCAAACTTGCCCT[C/G]TTCCTCACACTGCCG | 89910 |
rs532217238 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109530503 | GCCTGTCCATAAGTG[C/T]CCACGCTAGCACATT | 89910 |
rs532241013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487838 | AGCTGCTTCCCCTCT[C/T]TTACTGTCGATGAGC | 89910 |
rs532262695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508559 | TATAAGATACAATGG[A/C]CCTCAGGCAGTTATG | 89910 |
rs532446669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109529116 | CAGTGAGCTGAGATC[A/G]CACCACTGCACTCCA | 89910 |
rs532465919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533348 | CTCCATACGGCTGGC[G/T]AGACAGCAGTTACAA | 89910 |
rs532484584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109528581 | ATGCAAGGCTGGGTG[C/T]GTTGGCTCACACCTG | 89910 |
rs532486347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534460 | GGGTAGTGGTGCCAG[A/G]GCAGCGCCCTGCACT | 89910 |
rs532495094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527162 | TCAAATGCCACAGAC[A/G]GAGGTCCTTAGACAT | 89910 |
rs532501662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533041 | GGTGCCACCAGCCTC[C/T]GCCTCGCCCTCACCG | 89910 |
rs532558236 | snp | C/T | 2.23786e-05 | 0.00334497 | intron-variant | UBE3B | GRCh38.p7 | 12:109486622 | AAACCAGAAACAGTA[C/T]GTATGTCATTTTCAC | 89910 |
rs532560135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478729 | GAGGTTGCAGTGAGC[A/G]GAGTTCGCGCCGCTG | 89910 |
rs532622621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486087 | GTAAGTGGACGGGAG[C/G]CGCAGTGTCTCCCAC | 89910 |
rs532765001 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494367 | CCCAAACTTGCCCTG[C/T]TCCTCACACTGCCGT | 89910 |
rs532800526 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109515455 | GCTCACCACAACCTG[C/T]GCCTCCCAAGTTCAA | 89910 |
rs532808426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513204 | CCTCCTCCTGGACCC[A/G]CGTGTCTGTGAAATC | 89910 |
rs532837652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515063 | GGACTACAGGTGCTC[A/G]CCACCACGCCCAGCT | 89910 |
rs532935357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109538448 | CCACTTCCTGCCCCA[C/T]GTGGAGGGCAGCCTC | 89910 |
rs533020177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109492030 | TTTTCTGGAAAGAGC[C/T]GGATAAATATTTCAA | 89910 |
rs533029067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520411 | GTTCTGGGGCTGTGC[A/G]TGTTGAGGTCTGGAT | 89910 |
rs533049830 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476028 | ACCTATAAGAGCCCT[C/T]TGACTCCCAACTCCT | 89910 |
rs533084604 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477795 | GGCCGGTAGGGCCTG[A/C]GGTCCGGCCTGCGGG | 89910 |
rs533120992 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543758 | GAATCACTTGAACCC[A/G]GGCGGCAGAAGGTTG | 89910 |
rs533132565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109492700 | GCGAGCCGTGATTGA[A/G]CTTCTCCAGCCTGGA | 89910 |
rs533184483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542285 | TGCTTTCAGCAGTCC[A/G]TGGGTATGGGCCTGG | 89910 |
rs533217331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497405 | AATTATGAGTTATTG[A/G]TGAGTTACCACAGAG | 89910 |
rs533226424 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504874 | CAGTAGCGCAATCTC[A/G/T]GCTCAACTGCAGGCT | 89910 |
rs533324312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525984 | TGGCCTTTTTTCACC[A/T]TTTTAGTAAACGCAC | 89910 |
rs533359971 | snp | G/T | 1.6964e-05 | 0.00291233 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477271 | CTACCATGAAAAGTC[G/T]GAGGACGCAGGAGTC | 89910 |
rs533407850 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535994 | ACCACCAAGGTTGAT[A/G]CCGGATTCGAAGCCA | 89910 |
rs533414698 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490992 | TGCTCTTTTATGTAC[A/C]AATGAATATAAAGTT | 89910 |
rs533470638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109511376 | TGCCTTTCCATCCTT[G/T]CTATGGCAATTGGAG | 89910 |
rs533517526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109541611 | AACAATTCCATTGGC[C/T]CCTATATTGGTTTCC | 89910 |
rs533579625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109491696 | CAGAACATGTTTAAA[C/T]TGTCAAGGGGAACAC | 89910 |
rs533662486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531658 | TGAAGAGGCCCTCAC[A/G]CAGTCCAGCAGATAA | 89910 |
rs533700712 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109531056 | TATTAAACAATTGCT[C/G]TTCCTCCAGTATGGA | 89910 |
rs533704550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536713 | GCATATGATGGCTGC[A/G]TTCTGCATTTCATTC | 89910 |
rs533750088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109537641 | CCCAAAACACACATC[A/G]CCAGCCTCCAGTGTG | 89910 |
rs533822957 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109526818 | GGAGGTTGCAGTGAG[C/T]CAAGATCGCACCAGC | 89910 |
rs534020993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478166 | TAAATGGAGTAATTA[G/T]CAGGTTTCACAGAGG | 89910 |
rs534045429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485730 | TTGCCAGATTGATAC[G/T]GTTTTTTGAAAGAAG | 89910 |
rs534108137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109492104 | CATCTTGAAAGCAGT[C/T]GTAGATTGTACATAC | 89910 |
rs534120612 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109532684 | TTTGCAGGAATAACG[C/G]AGGGGCTGCCGCTTG | 89910 |
rs534135240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525556 | CTGTAGGGTTATAGA[A/C]TCTTCACAGAATTTC | 89910 |
rs534248481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109490467 | TGAGAAGTAATGTTG[A/G]CTTTGCCCTTCCTTC | 89910 |
rs534277688 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBE3B | GRCh38.p7 | 12:109531165 | CACACCCACAGTGTC[C/G]CAATAAAACACACAC | 89910 |
rs534314918 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109530733 | TGATGTAATAATTTA[A/C/T]GCTGAAGAAACTGAA | 89910 |
rs534365751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109512282 | GGGGAGTCAGACGGA[A/G]TGAGAAGTCCAGGGC | 89910 |
rs534440510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109540809 | TTTACAACAAGAACA[C/T]TGTAGCCAGAACTTG | 89910 |
rs534485436 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535946 | TGTGTTGACAGCCAC[C/T]CACCCTCTCCCACCT | 89910 |
rs534521305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109541799 | TTCTGGTGGCCCCTG[C/G]GTGCTTGGCTGTAAC | 89910 |
rs534542159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496837 | TCCATGGGTTGTCTT[C/T]TCACTTTCTTGATAG | 89910 |
rs534557248 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517004 | TGATCTGAAATTAAG[A/G]CTCTGGGAGCAGGAA | 89910 |
rs534563601 | snp | A/G/T | 0.000103226 | 0.00718347 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510388 | TTCCAGTCTGTCCAC[A/G/T]GGTGGCTTATGGTGC | 89910 |
rs534577988 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109487866 | AGCTTTGAGGTTTGA[A/G]CTCAGTGGTCTCCAA | 89910 |
rs534778978 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511945 | TTAAGGAGGCCTCAG[A/G]GAATGGTCACATCCC | 89910 |
rs534861882 | snp | C/G | 1.65266e-05 | 0.00287455 | intron-variant | UBE3B | GRCh38.p7 | 12:109530080 | GATTTAAAGTAAGAG[C/G]CGGGTGGGGGGAAGG | 89910 |
rs534863176 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526984 | GGAGTTTAATAACGG[C/T]CCTAGATGCTGACAG | 89910 |
rs534898577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109529517 | AATTGATTTATGTCC[A/C]GAAGAATGAGATTAA | 89910 |
rs534906867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504321 | CAGCCAAATGCCCCC[C/T]GGGAGGCAAAATCAT | 89910 |
rs534917122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109503487 | AAAAGATAGGGTTGC[A/G]AAAAAAAAAGGAAAA | 89910 |
rs534917440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109510826 | TTTAGGTTTTTTGGA[A/G]AGTAATGGGGTGGGG | 89910 |
rs534963104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109488151 | ACCGAGGCACAGAAA[A/G]GTTAAGAAACTTGCC | 89910 |
rs535059609 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109541912 | TCCTTGAATTAGGAC[A/C]CACCCTCACCCAAGA | 89910 |
rs535195404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109511082 | TATGGTCATGTTCCC[A/G]TCAGACTCTTGAGAA | 89910 |
rs535206927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482524 | TATTTTCATGTGGGT[A/G]CTACTTCAAGTAAAG | 89910 |
rs535261568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531231 | AATAAAGTGGCTGAC[A/G]TTAACTGGTTCCCCA | 89910 |
rs535339398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487585 | AATGCCTTAGGGCCA[A/G]GTGAGCAGGGTATTT | 89910 |
rs535399093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542588 | TTCAGATGAGGTCAT[A/G]TAGGAGTAGGGTGGG | 89910 |
rs535449420 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535449 | TTCTGCGTCCTCAGC[A/G]GGCTGAGCTGCCAGA | 89910 |
rs535481073 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540619 | AGGAAGACACTTGTC[A/G]GAATGGCACATGGAT | 89910 |
rs535481493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109481036 | CATGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 89910 |
rs535504391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496001 | ATTCCCAAAAATCAC[C/T]ACAATCTAATTCCAT | 89910 |
rs535518805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495500 | GAGACCAGCTTGGTC[A/G]GGGAGACCCTAACCC | 89910 |
rs535545422 | snp | C/G | 3.97804e-05 | 0.00445967 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510415 | GTGCTGTACGAGCGG[C/G]ACTGCCGGCGGCGCT | 89910 |
rs535575586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502492 | TGTTCTTCTACTGAG[A/T]GTGTTGCAAAACTCT | 89910 |
rs535603518 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531765 | GGGAGAATCAGTTCA[C/G]TTTTCCCAGAAGTGC | 89910 |
rs535689858 | snp | C/G | 0.00302733 | 0.0387879 | intron-variant | UBE3B | GRCh38.p7 | 12:109533785 | AGCCCCTTTCTCTTT[C/G]CTTCCTCAGGGAAGG | 89910 |
rs535697686 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490556 | CCTGTGAGGTGGTCC[A/G]TTGGCAGAAGCTGGT | 89910 |
rs535707959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497640 | AGTATGGCATCAGCA[A/G]CTGGACCATCACTGA | 89910 |
rs535709820 | snp | A/G | 3.30267e-05 | 0.00406353 | intron-variant | UBE3B | GRCh38.p7 | 12:109490026 | GACTCCTGCCCCCCA[A/G]TGTGCAACTTCTCCA | 89910 |
rs535738848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524649 | TCGCCCATCCTCCTC[C/T]CCTCTTGCCAGGAGG | 89910 |
rs535745471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482602 | TTCATTTCAGTGTTT[C/T]TAACTGGGCTGATTG | 89910 |
rs535763165 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109504936 | TCAGCCTCCCGAGTA[C/G]CTGGGATTACAGGCG | 89910 |
rs535771809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497121 | TATCTTTTTTTGATT[A/G]TGGAAGCAATACATG | 89910 |
rs535781541 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536041 | CCTCTGCTCTCCTCA[A/G]AGACGCAAAACATTT | 89910 |
rs535803845 | snp | C/G | 0.00031523 | 0.0125505 | intron-variant | UBE3B | GRCh38.p7 | 12:109530109 | GGGTGAAATTCCTTG[C/G]CCTCCCAGAAAGCCA | 89910 |
rs535806594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478908 | AAACCTGGTGGCCCA[A/G]CTTTTCCTACTGCAC | 89910 |
rs535810361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109529598 | TGGGGAATGTCTCCT[C/T]GTGATTCCCGACATA | 89910 |
rs535845992 | snp | A/G | 3.48815e-05 | 0.00417607 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534734 | GAGCGTCCTCCGCGA[A/G]AAGCTGCGCTACGCC | 89910 |
rs535892254 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109488223 | GCCCAGAGTCCTAGT[C/T]ATGCTCAATTGCATT | 89910 |
rs535919379 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506568 | GTTGGCCAGGCTGGT[C/G]TCAAACTCCTGACCT | 89910 |
rs535920092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487324 | CAGACATACACAGGA[A/G]CCACTTCCACTTTGC | 89910 |
rs535993159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109540183 | GTATGTGCAGGGTTT[A/G]GGTGGGGGATTTTTG | 89910 |
rs536003780 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520201 | TGGGCCTCTCAAGTC[A/G]GGCCAACAGACTCTT | 89910 |
rs536060468 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481576 | CAGTGAGGAAGATGT[A/G]TGATACCACACCTAT | 89910 |
rs536077410 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3B | GRCh38.p7 | 12:109501727 | CATGATCATAGCTTA[C/T]TAGCCTCTAACTCCT | 89910 |
rs536093921 | snp | A/G/T | 6.61008e-05 | 0.00574862 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509640 | AACAGATTTCATTCA[A/G/T]ACTGGAAGAGCTGGT | 89910 |
rs536164716 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542865 | TAAGTCCCCGAGTTT[A/G]TGGTGCTTTGTTCCG | 89910 |
rs536316538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109480163 | AGAACCTTAGTAACT[A/G]TCCAGGTGGGAGCCT | 89910 |
rs536344224 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109522559 | CCTGGGCAGCACTCC[C/T]CGCATACCCCAGGAA | 89910 |
rs536361522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513785 | GAAAATGGGGCCCTC[A/G]TCATCTCCTGCCCCT | 89910 |
rs536409998 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485713 | AGGAATCCAAATCCA[C/G]TTTGCCAGATTGATA | 89910 |
rs536544881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109508978 | TAAGGAAGGCGTGAA[C/T]TGAGGTGTGAATTAA | 89910 |
rs536563176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515810 | TGATTCTTGAGCCCA[C/G]GATGGGGCAAAGAGT | 89910 |
rs536568501 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109508018 | GGGTTTAGATCATGG[C/G]TCAGCCATTTATTCA | 89910 |
rs536579251 | snp | C/T | | | stop-gained, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501480 | AAGCTACTGGAGAGC[C/T]AGGAGCCAGCCCACG | 89910 |
rs536582594 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109538689 | TGGCTCCTGCTGCTG[A/C]TGATGATCCCAGCAG | 89910 |
rs536685587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507309 | ATAACACTGGGCTTC[A/C]GAAAATGGAAAGCAA | 89910 |
rs536716721 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522907 | CCCATTAGGACCCAC[C/T]CGAGCACATGGCATA | 89910 |
rs536720386 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109532816 | GGCTCTGGGGCCTCA[-/T]TTTTGTCAGTGTGCT | 89910 |
rs536721582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109481863 | ACTTAGTGTTTTTTT[A/T]AAAAAGTTGAAACCC | 89910 |
rs536742081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523845 | GAGATACTGCCCTCC[A/G]GATTGGAAACTTAGG | 89910 |
rs536754785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538862 | AGGATCCAGCCAAGG[C/T]GTTTCCAGGCCCCTG | 89910 |
rs536866851 | in-del | -/TGT | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109502849 | TTGTACCTAAAAACC[-/TGT]TGTTAATGTTTTTCT | 89910 |
rs536881474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109503334 | TGTTCCTCTTAGAGA[C/T]TAGTCCACCTCAGTT | 89910 |
rs536887092 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542761 | GGAACAGATTCTCCT[A/T]CACAGCCTGGAGAGG | 89910 |
rs536906153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109493416 | CCTGTCCTGGTGTGG[C/T]TGTAATTCACATATG | 89910 |
rs536908032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109500676 | GCCTGCTCTCCGCTC[C/T]ACTTCCTCTTCTTGG | 89910 |
rs537012284 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489197 | CCAGGGACTTTAGGT[A/G]CTCCCTTCCTCACAG | 89910 |
rs537055901 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493089 | AACTATTTATCTAAT[A/G]AACAATTGTGCCTTC | 89910 |
rs537138482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109516057 | CATAATATTGATTTC[C/T]CTTAAAGCAGGCACA | 89910 |
rs537156034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507450 | CACCTTCTTTTCACG[C/T]ACATTAAATGTTCAT | 89910 |
rs537181115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523251 | GCACAGTCTGTCGGC[A/G]TTTTCCCCTGGCAGC | 89910 |
rs537203310 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541249 | GCAGTTCCCAGATAA[A/G]GAGGCCGCAGAAGAC | 89910 |
rs537217222 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109512536 | TTAGAAGAGTCTTCT[A/G]GGAGTCTAGGTTGTG | 89910 |
rs537224061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109519989 | CACTGGCATACTGCT[C/T]GTTTGCTTTGTGATG | 89910 |
rs537230063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109541040 | GAACTGCCTCTGAGT[A/C]CACCATCCTTGCAGC | 89910 |
rs537255279 | snp | A/G | 0.000188519 | 0.00970691 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534096 | AAAAACCCAGTGGCC[A/G]CCTCTGGGTGTAGCT | 89910 |
rs537262687 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3B | GRCh38.p7 | 12:109540299 | TACAACCTCCGCCTC[C/T]GAGGCTCAAGCAATC | 89910 |
rs537280536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495581 | AGTAGGAAATCAGGG[A/G]TCTCACAGCCTTCAG | 89910 |
rs537324994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539230 | GACAGAATGAGACTC[C/T]GTCTCAAAAACAAAA | 89910 |
rs537336443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109510268 | CTTGATGACAACTGC[A/G]GAAGACAAGAGCTGT | 89910 |
rs537348722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509777 | GAGGCCGAAGAGTCT[A/G]TGGCATCAACTGATT | 89910 |
rs537393126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533678 | AGGCAGCTGGACCCC[C/T]CAGAGCCAAGTGAGG | 89910 |
rs537414487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526909 | CAAAATAAGAATTGA[C/T]CATTTATTTTTTGCA | 89910 |
rs537452720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532708 | CCGCTTGGAGAACGC[C/T]GGGAGTTCCCAGGGG | 89910 |
rs537484212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109500839 | GCCTGGCCGTACTCA[A/G]GGGTGGCGGCTATTA | 89910 |
rs537505112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109492313 | TTTCAAATGCTCAGC[A/G]GCCACATGTAACTAG | 89910 |
rs537547506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109508104 | TGCTAAGCAGATCTT[A/G]AGACACCCTGGGCAA | 89910 |
rs537584903 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489739 | CCTACCAGGAGAGAG[A/T]GAGTTCCAGGTACGC | 89910 |
rs537604664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522376 | CACCTTCAGTGGGAA[A/G]TCACCGCCTGTTCCT | 89910 |
rs537604890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109514799 | TGGAACCTCTCAGGG[C/G]TTTTGGTTCTACTCA | 89910 |
rs537638663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109481044 | CGGGAGGCGGAGCTT[G/T]CAGTGAGCCAATATC | 89910 |
rs537699095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486963 | TTGTGCTCTAGAATA[A/T]ATTCAGTAACGTGGC | 89910 |
rs537699246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494603 | TAAGCAGTGCACTTA[C/T]AGACTTTGTCACCCA | 89910 |
rs537724977 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495730 | TGGGCCGAAATAAAG[A/G]GATGGGCTCTGGCTA | 89910 |
rs537727457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510140 | CTAGTGGGAGGCAGC[A/G]TGAGTGATTTTGTCT | 89910 |
rs537819400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109533122 | GCTCTGTTCCTCTTA[A/G]CAATCCCACAGGAGA | 89910 |
rs537893686 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526107 | ACACATTCCCCTCCA[C/T]GACATCCCGAAGTCT | 89910 |
rs537965854 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491243 | ATTTTGTCAGAATTT[A/G]TGGGAAGCATTGTTC | 89910 |
rs537966598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499083 | ACGCCTCAGCCTGCG[A/T]GATTACAGACTTGAG | 89910 |
rs537986548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109537997 | TGAGCCACCGCGCCC[A/G]GCCAACATTCTGGCT | 89910 |
rs538009402 | snp | A/G | 3.30764e-05 | 0.00406659 | intron-variant | UBE3B | GRCh38.p7 | 12:109498214 | AGTTTCTGATTTAAC[A/G]GTCTGCTATTCTTTG | 89910 |
rs538024855 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535732 | TCCCAGGAAACTTGG[A/G]TCTTGCTGCCCATCC | 89910 |
rs538153743 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109505782 | CACCCTCTAAGTATC[A/C]TTCAGTAGCTCTGAT | 89910 |
rs538173821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527278 | GTCCCTAGAAGCAAA[A/T]CCTCTCAGTGCATGG | 89910 |
rs538224549 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109479889 | TTTGGGAAGAGGCTC[C/G]CTCTTCCCCTTCTAA | 89910 |
rs538245901 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477379 | TTCCGCTGTCCGCAC[C/G]CCACTTCCGCCCCGC | 89910 |
rs538285802 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479023 | TCCTGCCTCTTAGTT[A/G]TTACAGCCTTGACTC | 89910 |
rs538410724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109508128 | TGGGCAAGGGATCAC[A/G]GATTCAACCTCTCTG | 89910 |
rs538415523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515655 | ATTACAGGCGTGAGC[C/T]ACTGTGCCCAGCTGT | 89910 |
rs538463240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109543306 | ACTGGAATAATCCAC[A/G]GACCTGTCACCAGGT | 89910 |
rs538466064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109506470 | TCTCCTGCCTCAGCC[C/T]CCTGAGCAGCTGGGA | 89910 |
rs538491904 | in-del | -/AA | 0.00716266 | 0.059414 | intron-variant | UBE3B | GRCh38.p7 | 12:109495708 | TCCTTATGGGGAAAC[-/AA]AGGGATGGGCCGAAA | 89910 |
rs538519197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109513520 | TCTTAGGACATAAAT[A/G]TTTGGGACCTAACTA | 89910 |
rs538576988 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523709 | GTGAGACAGCTGAGG[A/G]CCCCTGGCTTGGCAG | 89910 |
rs538612484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527994 | CTCACTCTCCCCACA[C/T]AGGCACTGGCTGCTA | 89910 |
rs538647225 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109527483 | TGAGTCATTTGAATC[A/G]GATGCACGTCGCAGT | 89910 |
rs538783361 | in-del | -/TTTA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526057 | ATGGATGTACCAGTG[-/TTTA]TTTAACCGTCCTACT | 89910 |
rs538787908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533187 | CTGGGCATTTGTGCT[C/G]TTCCTACTCTGCAGT | 89910 |
rs538922024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515274 | ACAATCATATTTGCC[G/T]AATAGAGTTAACATA | 89910 |
rs538955267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109499155 | GTGCGAATGTTCACA[C/T]GAGTGACGTTGACTA | 89910 |
rs538958715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109522459 | AGTCTGTGTGGCCTT[C/T]GCAGTGGGCTCCAGA | 89910 |
rs538994423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513615 | GTGATAGAGGTGCTG[C/T]GAATAAGAAAGTCAG | 89910 |
rs539012458 | in-del | -/CTC | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109530187 | TCTCCAGATCTCCTT[-/CTC]CTCCCTGGACTGGCT | 89910 |
rs539078172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505686 | ACCACATCCTCCTAC[C/T]CTTGAAAATGTGAGG | 89910 |
rs539081801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542649 | AGAAAGAGAGGACTC[A/G]GCCATGTGAAGACAG | 89910 |
rs539152935 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109505050 | TCCTGTGTGTCCAGC[C/T]TTTTAAATGAGCTCA | 89910 |
rs539155624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526699 | AACATGGTGAAACCC[C/T]GTCTCTACTGAAAAT | 89910 |
rs539166851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109511682 | TAGAAAGGATGGGGT[A/C]AAGAGGAAGCCGAGG | 89910 |
rs539206639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538574 | ACCTGGCACCAAGTA[C/T]GCATCCGTTAGTCCT | 89910 |
rs539231100 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109526106 | AACACATTCCCCTCC[A/G]TGACATCCCGAAGTC | 89910 |
rs539261315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532099 | CGCCCCTCCCCGCTC[A/G]CAGGAGCGGGAAAGC | 89910 |
rs539329897 | in-del | -/GACAGA | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109502433 | ACTAATGCATAATTT[-/GACAGA]GTTACCTGCCTGTGG | 89910 |
rs539332381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507180 | TCCCTGATTTAAAGC[A/G]TAAATGCTAAGTCAG | 89910 |
rs539344578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109506510 | CTGGCCACCACGCCC[A/G]GCTGATTTTGTATTT | 89910 |
rs539361108 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109514681 | GTTCTCAAAAGTCCT[A/G]CAGTTCCCCTGCCAT | 89910 |
rs539361227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527358 | GAGAAGCAGACATTG[G/T]CCCCCTTGTCAGTTT | 89910 |
rs539393486 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536952 | CCTCTCACCCACTTC[C/G]CAGAGGCAGCTGTCA | 89910 |
rs539407162 | snp | A/G | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533533 | CTCCATTCTCCATCC[A/G]CTGCGTGGAGGTGTC | 89910 |
rs539433876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109483361 | TGCATGAAAGAGCCT[A/G]TAGGAGGTAGGGACT | 89910 |
rs539440876 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109528379 | CTGGAAGGAGGAGCA[A/G]TGATAGGAAAATCGT | 89910 |
rs539495832 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109482695 | CTCCGGGGGTCAGTG[C/T]TGTGTGCTTTAGGCT | 89910 |
rs539524264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504643 | TGGGAGCATCAGCTG[A/C]GGGATGGAGTGTAAA | 89910 |
rs539570748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496106 | TGGCAACAACTAATC[C/T]ACTTTCTATCTCTTT | 89910 |
rs539628070 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3B | GRCh38.p7 | 12:109485621 | TGGCTACTGGCTGTG[A/G]GGCAAAAGTCAGTAT | 89910 |
rs539727915 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478400 | ATTCAAAAGCATCCA[C/T]CTTAGATAGGCTGTA | 89910 |
rs539740449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518385 | AATTCAGATCTTCCA[C/T]GTTGTGAACTAATTG | 89910 |
rs539760131 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490672 | TTAAGTCTGGCATTA[C/T]TTGTATTAGCTGTTT | 89910 |
rs539778151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525050 | GAGTGCAGGTCCAAG[A/G]GCCGCTCAGGAGAAA | 89910 |
rs539810272 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502131 | ATATGTTACATTAGG[C/G]CCACTGTGGCTACCT | 89910 |
rs539876342 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531955 | TGTGCCTGCCCTTTT[G/T]TGCAGCTGCATACAG | 89910 |
rs539880286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496665 | CTTTTCATGTGCTTA[C/T]TAACCATTTGTGTAT | 89910 |
rs539887135 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506216 | GGGGGGAAGCTTTGC[C/G]AAAGGTGGCGAGCCT | 89910 |
rs539902342 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531198 | TTGCTTAGGCTGATA[C/T]CAAGATGTATTTTTG | 89910 |
rs539907300 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109483769 | CAATTAATAGCAGAT[A/T]AATGAGTTTTTTCTC | 89910 |
rs539982376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109530914 | CATACCTGTTGTGCT[C/T]GGCACTCCGTCCTCC | 89910 |
rs540046316 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528623 | CTTTGGGAGGCCAAG[A/G]CAGGTGGATCACCTG | 89910 |
rs540120107 | snp | G/T | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109525406 | TACAGAATAGCTCAC[G/T]GGCAGGGTGTTCCTG | 89910 |
rs540126857 | in-del | -/TT | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109527435 | TGGAGCATCAGTCTC[-/TT]TAGTGACAAGTGAGG | 89910 |
rs540147216 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109511944 | TTTAAGGAGGCCTCA[A/G]AGAATGGTCACATCC | 89910 |
rs540162340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526259 | GCCATCTTAATTCCA[C/T]CATTATCATGGATGT | 89910 |
rs540237490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109510532 | GAGCACTCAGCTCTC[A/G]TGTTCTAGGGCAGAG | 89910 |
rs540252832 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536341 | GTGCGCACGCTGGGC[A/G]GGTTCGTGCATACAT | 89910 |
rs540283759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475443 | GATAATACCAGTGCA[C/T]TCTCCAGCCTGGGCG | 89910 |
rs540346480 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109482766 | TGATTTAGATAAAAA[A/C]TTAGTATATAATTTA | 89910 |
rs540360927 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536523 | AATTTCATTTAAATT[A/C]TTTTCAGCAGCTGGA | 89910 |
rs540446508 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536180 | TCTGGAAAAGAGTGT[A/G]TGCTCTACTTTGATG | 89910 |
rs540460635 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109497271 | TATATTTGTGTTTAT[A/G]TTTCGAAACATTATA | 89910 |
rs540484197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542111 | CATGCCATGAACCAC[C/T]ACATGCTCACAGATC | 89910 |
rs540512076 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109520171 | TGTCTGAAGACATCA[C/G]TTTCACCTGGTGATT | 89910 |
rs540523876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109504692 | AGGGCAGGTTTCCCA[A/G]AGATGAGCAGAGGGA | 89910 |
rs540550055 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477206 | TATACTCTGCTGCTG[C/T]CCAGCTCCCTCGGCC | 89910 |
rs540572148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109518582 | GTCTCTAGAAATCCT[C/T]AGCCCCACTACCCAT | 89910 |
rs540582384 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496245 | TAGCATGGATCAGTA[C/G]TTCATGCATTTTATG | 89910 |
rs540629914 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109532826 | CCTCATTTTTGTCAG[-/T]GTGCTGAGAGGTTAT | 89910 |
rs540796535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109542715 | GAACGCAGGGACTTC[C/T]AGCCATCACCCATAG | 89910 |
rs540933232 | snp | C/T | 1.71675e-05 | 0.00292976 | intron-variant | UBE3B | GRCh38.p7 | 12:109511328 | ACTCAGAGCTGGGCC[C/T]CGATGTGTCTTTCTA | 89910 |
rs540991838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502770 | GTATAAGAATCCCAT[A/G]TAAGATTTGAATATG | 89910 |
rs541005443 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535175 | TTTTGCAGCATGGGT[C/T]GAGTGTACAAAGCCT | 89910 |
rs541014981 | snp | A/G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512258 | CCCCATAACCTGGGC[A/G/T]AGGTGGTTGGGGAGT | 89910 |
rs541097940 | in-del | -/TTC | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109514907 | TCAGTACCATCCCCT[-/TTC]TTCTTCTTTTTTTTT | 89910 |
rs541102625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509923 | TTGCTCTCCCAGGCT[C/T]CCTTCAGGATTTGCA | 89910 |
rs541104296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109501858 | TGTAGAGATGGGGGC[C/T]TTACCTTATTGCCCA | 89910 |
rs541145610 | in-del | -/AG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514221 | TACCCAGAAGGCCTA[-/AG]AGGTGTGGAGTGGGC | 89910 |
rs541154471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494230 | AAATTAAACCCAGGC[C/T]ATTTAACTCCAGAAC | 89910 |
rs541167242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109533351 | CATACGGCTGGCTAG[A/G]CAGCAGTTACAACAC | 89910 |
rs541190391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109530292 | GGGGGTTCTCTGAAG[C/T]TCTAGGAGATGGGGT | 89910 |
rs541192354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524307 | AAAGTCACGAATGAC[C/T]TTCTTTGCGTCAAGC | 89910 |
rs541208353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539300 | CATTCATAGTTCTCA[C/T]CACCCTCTGGAGCGT | 89910 |
rs541222485 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535584 | TGCCTGTTCCCCAAA[A/G]CCTGCTTGTCCCGCG | 89910 |
rs541227244 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109529766 | TGTTCTGATGAAACA[C/T]TCTGGTACTATTTGT | 89910 |
rs541233789 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109518993 | CTGGGCATTGTTTCC[-/T]TTTTTTATGGTTAGT | 89910 |
rs541259831 | snp | C/T | 8.25648e-05 | 0.00642461 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511262 | AGAAAACGGGCACAG[C/T]TGATCCTGCAGTACA | 89910 |
rs541309181 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479470 | CCTAGAGAGGATAAG[C/T]AACTTGGCCAAATGT | 89910 |
rs541350140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109523354 | CTCTGTCCCTTCCCT[A/G]CTCAGAGCCCTCTGG | 89910 |
rs541444415 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535618 | GACGGCTGCCTTTGA[C/T]CCTGCTTATTTGTCT | 89910 |
rs541509610 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482005 | CACAGAGGTCCCTTG[A/G]TATGTTCATGTGGTG | 89910 |
rs541719988 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109482863 | CCTTGGCAGGATGGT[A/G]ATTGTAAGGACAATG | 89910 |
rs541736923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522707 | GAAACAGTCTATGTG[C/T]ACCGGCCTCAGTCCC | 89910 |
rs541830935 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535284 | CAAAGTTTCTGCCTC[C/T]ATGCCGTCCACAGCG | 89910 |
rs541878906 | snp | A/C/G | 8.24265e-05 | 0.00641929 | intron-variant | UBE3B | GRCh38.p7 | 12:109488537 | CTGGAATCAGAAGAC[A/C/G]TGTGTCTTAATCTTG | 89910 |
rs541904639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109503558 | TGTGCCTGAGTGTAC[C/T]GCACATATAAAATAA | 89910 |
rs541933384 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507895 | CAAGTGAGCAGTGTG[C/T]AGTAAATGTTCAGCA | 89910 |
rs541999783 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534362 | CCAAAAGCTTACTTA[C/G]TGCAGGAATTCTCTG | 89910 |
rs542013393 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109525166 | TTTCCATATCCATTT[G/T]CCAGATGCGAGTCCT | 89910 |
rs542028473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510041 | TGTGCCAGTGCACAC[C/T]TGAGATGAGAGTCCA | 89910 |
rs542146835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109516379 | ACGAGGTTTCACCAT[A/G]TTGGCCAGGCTGGTT | 89910 |
rs542211002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515341 | ATAGTATTTCCTGTT[A/G]TTGTTACTATTATTA | 89910 |
rs542308784 | snp | A/G | 0.00672148 | 0.0575809 | intron-variant | UBE3B | GRCh38.p7 | 12:109533757 | CTGCCCACGGACTCA[A/G]CCCTCTCTCGGCAGC | 89910 |
rs542334805 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109487156 | CTCCCGACCAGTTCA[A/G]AAATCCAGGTTTCTT | 89910 |
rs542419464 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487599 | AAGTGAGCAGGGTAT[G/T]TCCCTACCTGCACGC | 89910 |
rs542492304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109509378 | TCATCTAGGTTTTAA[A/G]CTCTACATGCATTAG | 89910 |
rs542522334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109500194 | AAGACAAATGATTCA[A/G]AGGGAATAGAAATCA | 89910 |
rs542567063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109508300 | TTATTATTATCAAGC[C/T]GACCCTGAGCAAGTT | 89910 |
rs542665961 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543631 | TGAAGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 89910 |
rs542671105 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109537422 | GTCCCAGTGGCTTCT[C/G]GCTGCTCCCCTGGCC | 89910 |
rs542693535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109491882 | TGGGCTTATTTAACC[C/T]GGGGTTGGCCCAAAC | 89910 |
rs542773787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109521798 | TTAAGGATGGGAGAC[A/C]TGAAGCTTTGAGGAG | 89910 |
rs542785310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533820 | CTGGAGTGGGGGTGG[G/T]TACGTGCTGTTTTTA | 89910 |
rs542820933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539675 | GTCATTATTTTGTTC[C/T]AGGGATCGAATTGAC | 89910 |
rs542855045 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501294 | TCCGAGTGGAAGGCC[A/G]TTAGGAACTGTGTGG | 89910 |
rs542860050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478550 | CTTTGGGAGGCCGAG[A/G]CGGGCGGATCACCTG | 89910 |
rs542983671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538287 | TAAATCCAGGACCCC[C/G]TTAAGCCTCAGGCTT | 89910 |
rs543029536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502093 | CACAATCAAGATTGG[G/T]TCATAAAAGCATGTC | 89910 |
rs543080786 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109499191 | TGAACGTTGAATAAC[A/G]GCGACTTCCCACGAC | 89910 |
rs543155461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505950 | GAGGAACACACCTTA[A/C]TGTATATTCAGTGAC | 89910 |
rs543160173 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514218 | GTTTACCCAGAAGGC[C/G]TAAGAGGTGTGGAGT | 89910 |
rs543204739 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109514757 | CTCCCTGTGTCCCCA[A/G]TCTGTCCCCTCTCTT | 89910 |
rs543210538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109527517 | GTGTTCCCAAGCATC[A/G]TGTTCCTCTCGGATC | 89910 |
rs543242631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109487736 | AAAGAAACAGACGTC[A/G]GGAGAAAAAGGGCCC | 89910 |
rs543249244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527031 | TCAGCACACTGTCCT[A/G]AACCCAGAGGGCACA | 89910 |
rs543266560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485922 | GCATAATACCTGCAC[A/G]TGCCAGGTACCCGCT | 89910 |
rs543304374 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542414 | ACTTTTTCTTGGAAT[A/G]TGTCACCAAATCCTC | 89910 |
rs543348672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532850 | AGGTTATTAGTCTCT[C/T]GCACAGGGTCCCCCG | 89910 |
rs543358101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109501793 | TATAATAGCTGGGAC[A/T]ACAGGCGTGTACTGC | 89910 |
rs543366313 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109539660 | ATGGCTGTGATAACT[C/G]TCATTATTTTGTTCC | 89910 |
rs543371980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109501189 | AGTCAATGCCCTTGA[C/T]GTACCAGCCCCTCAG | 89910 |
rs543410121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109509097 | CGATTTCAAATTAAT[A/G]GAAAGTAGAAAGGAT | 89910 |
rs543438554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109539414 | GAGTGCAGATCTTAC[A/G]AGGGCATTAGAGAGA | 89910 |
rs543468699 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109538403 | CGTGGGCTCTGGAAT[C/T]GCAGAGATGTGTGAG | 89910 |
rs543476177 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109532953 | TGCATGAATAAGGAG[C/G]CGGCAGGATGCCAAG | 89910 |
rs543547516 | snp | A/C/T | 3.34651e-05 | 0.00409043 | missense, synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499694 | GGAGACAGATGGGTT[A/C/T]GTGAGTTTGCTCACC | 89910 |
rs543577405 | snp | G/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109481734 | TCTGCGACACAGGCA[G/T]GTCCTCAGGTGAGAT | 89910 |
rs543590186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109529100 | CGGGAGTCAGAGGTC[A/G]CAGTGAGCTGAGATC | 89910 |
rs543629319 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534853 | CAGAGGCAGTGTGGT[C/T]CTGGGAATGTGACCA | 89910 |
rs543642429 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517402 | CACCTGAGCTAAATC[C/T]GTTGTCTGGAACTAC | 89910 |
rs543688929 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479680 | GGTATATAGGAAAGG[A/G]TGAGAAAAACTGTAA | 89910 |
rs543697938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539778 | TCCTCTGCTGGGCTT[C/T]GCTCAGCCCCTGGTG | 89910 |
rs543706827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109480244 | ACACCAGTTAGACTT[C/T]CTGACTATACACTCT | 89910 |
rs543904936 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527502 | GCACGTCGCAGTCCA[C/G]TGTTCCCAAGCATCA | 89910 |
rs543926104 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109492687 | AGTCAAGGCTGCAGC[A/G]AGCCGTGATTGAGCT | 89910 |
rs543993217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109484548 | AGGCTCGTGCCACCA[C/T]GCCCAGCTAATTTTT | 89910 |
rs544003079 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109515009 | AGCTCCACCTACCGG[G/T]TTCACGCCATTCTCC | 89910 |
rs544038253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109521961 | GGAGGCTGGGTCCCC[A/G]TTGTAGGAGGGCAGC | 89910 |
rs544053888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479246 | CCCTAACTAGATTGC[A/C]AGCTTCTTAAGGACA | 89910 |
rs544095767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513917 | CTCCCCTTAGTGGCA[C/T]GTGTGCTGCCCTCTG | 89910 |
rs544131889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513111 | TAGCCTCTCCACCTC[A/G]TCTTTGTTTGAAATA | 89910 |
rs544133526 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109520982 | TTTGCTTTTAATCAG[C/G]ACTCATTCAAAAGCA | 89910 |
rs544149439 | snp | C/G | 1.66081e-05 | 0.00288163 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486563 | CTGCTGTGATTTTCT[C/G]AAGCAGCTCAAGGTA | 89910 |
rs544159169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109506138 | TTTGTATAGTTCAGA[A/G]CATCCTACCACAGTC | 89910 |
rs544219741 | in-del | -/CT | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534898 | ATTGGCCCCTAGACC[-/CT]CTCTATAGCCATGAG | 89910 |
rs544232055 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491289 | ACATTTGTGACTGCT[C/G]AAACTTTTTCTTAAT | 89910 |
rs544250674 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109504800 | GGGGTTGTGGTTTGT[G/T]TCCAGCTTTTTTTTT | 89910 |
rs544361610 | snp | C/G | 1.81731e-05 | 0.00301433 | intron-variant | UBE3B | GRCh38.p7 | 12:109511346 | ATGTGTCTTTCTATT[C/G]CCCCACGTGGTTCCT | 89910 |
rs544363974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109506758 | CTGAGGATGCCTCCA[C/T]ATTTTGAGTCCTTAA | 89910 |
rs544383594 | snp | A/C/G | 0.00239393 | 0.0345281 | intron-variant | UBE3B | GRCh38.p7 | 12:109530837 | CAGAGAGGGGCTTGA[A/C/G]GGGCACGGCCGAGCC | 89910 |
rs544391829 | snp | A/G | 0.00219832 | 0.0330806 | intron-variant | UBE3B | GRCh38.p7 | 12:109521560 | GTATGAGGTAGGAAC[A/G]TTAAGAAACAGAGAA | 89910 |
rs544419885 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482805 | CTTCAGAAAAGCACC[C/T]GTTAGTGGACAGGAC | 89910 |
rs544436828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490927 | GGTACAAGCCACCAT[A/G]CCTGGCTCACAATAC | 89910 |
rs544461773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531516 | ATGTTTTCTTTTGGA[A/G]GTTTGGGCTTGAACA | 89910 |
rs544512298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497334 | ATAGATACACTACAT[A/G]TGTATATATTGTGTA | 89910 |
rs544546010 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524316 | AATGACTTTCTTTGC[A/G]TCAAGCTGTTCAGCA | 89910 |
rs544655263 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478480 | TTTCCTATTCTTTAA[A/G]TAAAAATTAGATTAT | 89910 |
rs544716818 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477826 | AGAACTGGGTCGTCA[G/T]TCCTCCGAGTGGTGG | 89910 |
rs544747162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109518700 | CGACTCCCTTCACAA[A/G]TATCATTGCTTATTG | 89910 |
rs544806082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109537243 | CTGGGTGTGCCAGGC[A/G]TTGTTCCCTTAGTGA | 89910 |
rs544842693 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536613 | GATGGCTCTTGATGG[C/T]TCTAAAAAGTTGTAG | 89910 |
rs544846335 | snp | C/T | | | missense | UBE3B | GRCh38.p7 | 12:109543597 | TAATCCCAACACTTT[C/T]GGAGGCAGATGGATG | 89910 |
rs544897060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505274 | GTGTCTGTTTGTGCT[C/T]CTCACACACATCTGA | 89910 |
rs544999962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109521065 | AATGATGCTGGGAGA[G/T]CTTCGCACAGAGGAG | 89910 |
rs545011514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109514898 | TTCCTCCACTCAGTA[C/T]CATCCCCTTTCTTCT | 89910 |
rs545039180 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109498083 | TTGTGTTAGTAGCCC[A/G]AAGAAGTGGGTTCTT | 89910 |
rs545040968 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487733 | TGCAAAGAAACAGAC[A/G]TCAGGAGAAAAAGGG | 89910 |
rs545042875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109520678 | GGCACTTCATGATTG[A/G]GAAGGCAGCGGGAGA | 89910 |
rs545168447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538890 | CTGTGGCCTCAGGGC[A/C]CCTCACTGTGCCCCC | 89910 |
rs545330124 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507429 | TAATGCTTTTCTCCA[C/T]AATCCCACCTTCTTT | 89910 |
rs545365246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109543354 | TGCAGACAGGCTCCA[A/G]GGGAGTGGCTCGGCA | 89910 |
rs545386705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505883 | TTCAGAGAGTGCCCT[A/G]TAAGATGAGAGGTAT | 89910 |
rs545400225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536730 | TCTGCATTTCATTCC[A/G]CCATATGCCTGGACC | 89910 |
rs545415767 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536116 | TCTCCACAGTCCTTC[A/T]GAGTTTCAGCTGCAT | 89910 |
rs545418009 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109530444 | TAGTAGTGTTCCCCA[G/T]GCCTGCCAGAGTGGA | 89910 |
rs545476248 | in-del | -/ACA | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109540797 | GGGACAAGTTATTTT[-/ACA]ACAAGAACATTGTAG | 89910 |
rs545515540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109512595 | TTTTTCTTTTTTTAA[C/T]GAAGTAGACATATTT | 89910 |
rs545520043 | in-del | -/GAA | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109519291 | ATGTTGAGATGCAGT[-/GAA]GAAGAGGAACGCTGA | 89910 |
rs545564854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109541896 | CTCTTAGAAGGACTT[A/G]TCCTTGAATTAGGAC | 89910 |
rs545590386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109519063 | AAGTCCTGTAGGAAG[C/G]CTCTTCTTCCCAGAG | 89910 |
rs545619892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532291 | TCAGGGAATGCTCGT[C/T]ACAGTGTGGAAACAC | 89910 |
rs545671482 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109491818 | TGGATCTACAGTACA[C/G]CTTCATGCTGAGAGC | 89910 |
rs545685627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498469 | AATTGGAAGTGCTTA[A/C]AATAAAAAACACGTA | 89910 |
rs545692074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518877 | TGTTATCCCAGTTGT[C/T]GTAATCTGGTGGCTT | 89910 |
rs545730841 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476289 | TTGCACAAAATGGAG[C/G]GGACTAGTCAACGTC | 89910 |
rs545756740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109537392 | GCTTCTGTCCTGACC[C/T]TCGGCAGCTCTGAAG | 89910 |
rs545764491 | snp | C/G | 1.67612e-05 | 0.00289488 | intron-variant | UBE3B | GRCh38.p7 | 12:109516923 | CTACCACAAGGAAGT[C/G]GGCCCTGCAACATGG | 89910 |
rs545840011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482921 | CTTCAATATAATGGA[C/G]TGTCTTGCATTCTGA | 89910 |
rs545877509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497189 | AAAAAGAAAAAAATT[G/T]CTCATAATTCTACAA | 89910 |
rs545888115 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109527924 | GGATCCTGCCACCCC[-/CT]GAGAGGACACGCATT | 89910 |
rs545898256 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532239 | TAACCACAGCCCCGA[C/G]ACACAGCATCCGTAG | 89910 |
rs545907592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109489646 | AAAAGGTGCTACAGG[C/T]GCTCAGAGGCCAGAG | 89910 |
rs545951376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109519276 | ATTCCCTGTGTGTGC[A/G]TGTTGAGATGCAGTG | 89910 |
rs545991561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109525735 | CCGACTATAAAGATA[A/G]TGAAACTTCTAACAA | 89910 |
rs545995032 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109511421 | TCATTCATTCAGCAC[A/T]AGGAAACGGTGGTTG | 89910 |
rs546020079 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477101 | CCAAAGCCCTTCCCC[C/G]ACCCCGGGCCTTTCC | 89910 |
rs546067614 | snp | C/T | 0.000154556 | 0.00878942 | intron-variant | UBE3B | GRCh38.p7 | 12:109510464 | GGCTGCGAAAGTGAG[C/T]TCCAGGGGTGAGGAG | 89910 |
rs546122887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517722 | GTTTGCACTTCAGAC[C/T]TTTTTATCACACTCC | 89910 |
rs546123838 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529075 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 89910 |
rs546237858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109510963 | AAACTTCTGTAAAGG[A/G]CCAGATGACTTTAGG | 89910 |
rs546293625 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109481673 | AAGTGAGAAGCTGTT[C/G]TCAGCCACGAGTCCT | 89910 |
rs546326253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523644 | GGGTGCTGGTACTGT[A/G]CACGTTCCATCCTCT | 89910 |
rs546378239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109543031 | AGCCCCAGCAGCTGG[C/T]CGCCCTGCCCAGGCT | 89910 |
rs546425021 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109542530 | CCCCACTACCTCAGC[A/C]TGTGGCCTTATTTGG | 89910 |
rs546453326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502940 | GTGCATTTAGAGCTT[C/T]ACTGAAATGCTCTTC | 89910 |
rs546475040 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536329 | TTCTGAACGTGTGTG[C/T]GCACGCTGGGCGGGT | 89910 |
rs546542889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518929 | CAGGGGCCTTTGCTG[A/G]ATTTGGACACAAGGG | 89910 |
rs546561926 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503096 | CGGGGGTAAACGGGT[C/T]GACTCTGCAGAAGTC | 89910 |
rs546664526 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476509 | CCCCACAGCTGAGAG[A/G]CAGATCTTGAAACAT | 89910 |
rs546674526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502328 | CACAGGCGGGGCTAG[C/T]GCTTCAGTGGCTTTC | 89910 |
rs546677078 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475742 | TTAAGAAACACTGTA[C/T]TGAGGCTTGTATAAA | 89910 |
rs546679136 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109516461 | GGATTACAGGCGTGA[-/G]CCCCCACGCCCAGCC | 89910 |
rs546769631 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109539351 | TGCTTCACGGCAGTC[A/G]TCCTGACTGTTACAC | 89910 |
rs546789045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505525 | GTTTCCTCTGTTTCT[A/G]TTTTAACCTATTTTT | 89910 |
rs546886525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496577 | TTTTTATTTAGCCAT[C/T]CCAGTGGCTGTACAG | 89910 |
rs546901106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504891 | CTCAACTGCAGGCTC[C/T]GCCTCCCAGGTTCAC | 89910 |
rs546977764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109488725 | CCATAGAGAGCTCAG[A/G]GACCTTTTTTCCTTT | 89910 |
rs546990178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495922 | CACGAACATGTCACA[A/G]TGCTGCAGAGATTTT | 89910 |
rs547082425 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508765 | ATGGAGCAGTGTTAG[A/G]AAATGTTCAGATAGA | 89910 |
rs547112776 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487291 | CAGTGTTCTGAAAAG[A/G/T]ATGGACAGGGGTGTG | 89910 |
rs547189069 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535776 | GGAACCCGGAAGCCC[A/G]TTGCACTGACAGAGG | 89910 |
rs547206933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109489736 | AGGCCTACCAGGAGA[G/T]AGAGAGTTCCAGGTA | 89910 |
rs547212009 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522135 | CGCATCAGTAAAGTG[A/G]AGATAAGAAAAGCCA | 89910 |
rs547276336 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109523727 | CCTGGCTTGGCAGCA[A/G]CCCAGCTAGGATTTA | 89910 |
rs547280897 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109481770 | GACTTTACTGCTGGG[G/T]CAGGAAGCGTAAATG | 89910 |
rs547285332 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542113 | TGCCATGAACCACCA[C/G]ATGCTCACAGATCCT | 89910 |
rs547310494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109480959 | CCCTTTATTCACTTC[A/T]AAGGCATAAACGTTT | 89910 |
rs547323568 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518962 | CGTCAGTAAGCTGAT[C/G]TCAGACTCATGCTCT | 89910 |
rs547389458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527728 | TAGAGAGGGCCCAGC[C/T]AGGGCCAGAGAGAGA | 89910 |
rs547396533 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109528600 | GGCTCACACCTGTAA[A/T]CCCAGCACTTTGGGA | 89910 |
rs547433467 | snp | C/T | 0.000185546 | 0.00963009 | intron-variant, missense | UBE3B | GRCh38.p7 | 12:109534017 | AAGCCTTCAGGGTTA[C/T]GGAGCTCTGTGTGTC | 89910 |
rs547437777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522096 | ATGTGCCTTCAAGTT[G/T]CTTTAGTTTTTAAGC | 89910 |
rs547467016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486863 | TGATCTACATTATTA[A/T]ACTAGTCAGGCCTCT | 89910 |
rs547479174 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109493872 | GCTTTGCCATCAAGG[G/T]TGGAGTGCAGTGGCA | 89910 |
rs547524613 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478266 | CTCCAGCTTAGCCCC[C/T]ACAGGCAATCTTGCA | 89910 |
rs547526124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109501301 | GGAAGGCCATTAGGA[A/G]CTGTGTGGGCTGGCC | 89910 |
rs547572406 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109515685 | TTACTGTTCTTATTT[G/T]TATTTAATAAAGTTC | 89910 |
rs547734479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109514700 | TTCCCCTGCCATGGA[A/G]GGGAGAGGTAGGAGC | 89910 |
rs547772813 | snp | A/G/T | 5.21076e-05 | 0.00510407 | intron-variant | UBE3B | GRCh38.p7 | 12:109521424 | CCTCTGCCTCTCCCC[A/G/T]TCTTTTTGCCTTGCA | 89910 |
rs547804434 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531135 | CCATTTTCTCAATAG[C/T]GTAAGACACACATAC | 89910 |
rs547842255 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533370 | CAGTTACAACACGGT[A/G]ACAGACAGAGCAAAC | 89910 |
rs547844541 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513201 | GCCCCTCCTCCTGGA[C/T]CCGCGTGTCTGTGAA | 89910 |
rs547903506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478732 | GTTGCAGTGAGCAGA[C/G]TTCGCGCCGCTGCAC | 89910 |
rs547915522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478129 | GTTCCCTCACCTCTC[G/T]GAGCCTCAGTTTCCT | 89910 |
rs547959172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539128 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCTG | 89910 |
rs547985395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109500638 | TGGGAGGTAAGTGAA[A/G]GAGAGCAGCACCTCC | 89910 |
rs548035147 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109510216 | CCTTTTAATTCTGTC[A/G]GTTCCACATATAATT | 89910 |
rs548118697 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505255 | TCTACTGACAACTTA[A/G]GAAGTGTCTGTTTGT | 89910 |
rs548182570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522826 | GCCCATTCTCTGTGC[C/G]TCTGTTTCCTCATCT | 89910 |
rs548192869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523787 | TGTCCTGACCACTGC[A/G]CTGTCCCCAGGAGGC | 89910 |
rs548320030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522254 | CCTCACCTTACTAAG[A/G]GGAAGTGAGTCTGGG | 89910 |
rs548403375 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532884 | CCCCAGCACATAGAC[C/G]ACTCTAAATCAGCAG | 89910 |
rs548411950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517118 | TTTACCCCATGAGAG[C/T]TAGAGTATCCTGGGC | 89910 |
rs548548564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109516469 | GGCGTGAGCCCCCAC[A/G]CCCAGCCTTGAGGAG | 89910 |
rs548569790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109515159 | ACCTCATGATCCGCC[C/T]GCCTAGGCCTCCCAA | 89910 |
rs548613701 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520217 | GGCCAACAGACTCTT[C/T]CCTGGGCCCTGTGCT | 89910 |
rs548625231 | in-del | -/GTGG | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109541915 | TGAATTAGGACCCAC[-/GTGG]CCTCACCCAAGATGA | 89910 |
rs548645445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508703 | CTGGTGAAGACATCC[C/T]TAATCACTGGATGGG | 89910 |
rs548649126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499069 | CTCGAACAATCCACA[C/T]GCCTCAGCCTGCGAG | 89910 |
rs548660432 | in-del | -/CATGGCCAGGCTCGGTAGCT | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109538951 | ATTCAGAAGAAGCTG[-/CATGGCCAGGCTCGGTAGCT]CATGCCTGTAATCTG | 89910 |
rs548758258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | UBE3B | GRCh38.p7 | 12:109534056 | GGCCCACTGTGGGTG[C/T]TCAAATGAGAGTCCT | 89910 |
rs548769864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502012 | TAGGTCACTAAGTTC[A/G]TATATAGCAAAACAA | 89910 |
rs548786572 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109527231 | ACAGATAAAGGGCTC[A/T]GCAGAATCTATCATA | 89910 |
rs548893124 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482902 | TATACATAAAACCAA[A/T]TATCTTCAATATAAT | 89910 |
rs548927015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533376 | CAACACGGTAACAGA[C/G]AGAGCAAACACGTGC | 89910 |
rs548937183 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109486721 | AAGAGAGGAATTTTG[A/G/T]TTCTGTTATCAATAT | 89910 |
rs548960750 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511823 | TACTTCAGGAAGGTC[A/G]TCTTGGCTGCAGCGT | 89910 |
rs548982411 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540687 | TGGCCTTCAGACCAC[A/G]GGCATGTGAAAGAGA | 89910 |
rs549074904 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537634 | CTGCCTCCCCAAAAC[A/T]CACATCGCCAGCCTC | 89910 |
rs549106621 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109506418 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 89910 |
rs549216654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109490479 | TTGACTTTGCCCTTC[C/T]TTCTCCCTAGTGCTG | 89910 |
rs549266816 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109519467 | AGATTTGAATCCAGT[-/A]AACGCTCCTTGAGCT | 89910 |
rs549285502 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477375 | TAACTTCCGCTGTCC[C/G]CACCCCACTTCCGCC | 89910 |
rs549334670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109493820 | CACCACATTCTCTTA[C/T]CTCCGTTTTATTTAT | 89910 |
rs549374486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531832 | GGCTCACGCTGGCCC[C/G]TCCTACAGAGGAAAA | 89910 |
rs549377592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109526012 | CACATTTTCATCATA[C/T]TGTTTAGTACCTGCA | 89910 |
rs549395038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484820 | GAGTGCAGTAGCACT[A/G]TCACAGCTCACTATA | 89910 |
rs549426023 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478632 | CTAAAAATACAAAAA[G/T]TAGCCGGGCGTGGTG | 89910 |
rs549434945 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109485406 | CACATGATTACGTAG[A/G]TGAGGACAGATAAGC | 89910 |
rs549446436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109493300 | GTCAGCACACTGAGG[C/G]CTGAACTTTCAAGCT | 89910 |
rs549456117 | snp | A/T | 1.65512e-05 | 0.00287669 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491169 | TTGGCATGTTCTTGA[A/T]TGCTTCCTCCTCTTG | 89910 |
rs549521815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513380 | TAGTTCAGAGTAGTT[C/T]GTGGTTTCAACATGA | 89910 |
rs549590060 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109500472 | ACTAAAGGCCTGGGG[A/T]GGAAATCCCCAAATT | 89910 |
rs549604804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520591 | AAGTCAGCCCTGTTA[C/T]TCTTTGCCTAAAACC | 89910 |
rs549651475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507825 | TAATTGCTAATGTGA[G/T]TACTGCAAACATTTG | 89910 |
rs549657175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487241 | ATGGGGTACTGCCAC[C/T]AGCCCAGCCTGGTCC | 89910 |
rs549694492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523061 | CTCCCTCACCTCTGA[C/T]AGTAATTGTGCTGAC | 89910 |
rs549733925 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109528495 | TAAAACATTTATTTG[C/G]ACTCTACTGATTTGG | 89910 |
rs549737612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109480612 | ACCATGATTGCACCA[C/G]TGCACTCCAGCTTGG | 89910 |
rs549739148 | snp | A/C/T | 0.00518141 | 0.0506816 | intron-variant | UBE3B | GRCh38.p7 | 12:109526643 | TTTGTTAGGCCGAGG[A/C/T]GGGCGGATCACGAGG | 89910 |
rs549739517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109519817 | AACTGTGCTCCTGTT[C/T]CCACATGTGACTTAG | 89910 |
rs549750695 | in-del | -/CTTT | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109482974 | AATGTTGAAATGGCC[-/CTTT]CTTTTTTGTGTGCTG | 89910 |
rs549889669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499522 | GCCCCTTATGTGGAA[A/G]TTTCTTGCTGCACAT | 89910 |
rs550009163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527972 | TGGGGGTGACAGTAG[G/T]TAGTCACTCACTCTC | 89910 |
rs550037942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109479771 | AATCTCAAGGAAGGG[A/G]ATAAGAGTAATTTCT | 89910 |
rs550176822 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478067 | GCCCCAGGACTCACC[C/T]AAACTGGAGTTCGAA | 89910 |
rs550185288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520617 | AAACCTTCTGCAGCT[C/T]CCATTACCTTCAGGA | 89910 |
rs550211406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532541 | GCCCCTGTATCCCCT[A/C]GAGAAGGGAGAACAT | 89910 |
rs550261725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504998 | GTATTTTTAGTTGAG[A/G]CGGGGTTTCACTGTG | 89910 |
rs550301464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109491931 | CCCCTGCCTTGTTTT[C/T]TGGATGCCGTTGATA | 89910 |
rs550301730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484947 | TTTTTTGTAGAGATA[A/G]GGTTTTACCTTATTG | 89910 |
rs550307304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518997 | GGCATTGTTTCCTTT[G/T]TTATGGTTAGTATTG | 89910 |
rs550392836 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543704 | CCGGCATGGTGGCAG[G/T]CACCTGTAGTCTCAG | 89910 |
rs550405951 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109514356 | ATGGGGAGAATGATC[C/T]GTACCCAACTGTCCA | 89910 |
rs550414338 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523397 | CTGCAGCAAGGCTTA[C/T]GGGCCCTCCCTGACC | 89910 |
rs550429850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109543157 | AATCTGAAACACCAC[C/T]GTTCAGGCCTCGGGA | 89910 |
rs550471391 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109498748 | GTAGATGGAAGAAAG[A/G]GTTTATGAATAGAAG | 89910 |
rs550528339 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109496588 | CCATCCCAGTGGCTG[G/T]ACAGGGGTATCTCAC | 89910 |
rs550543472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513533 | ATATTTGGGACCTAA[C/G]TACCTAGTAAAAAGG | 89910 |
rs550585222 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494937 | GCCCTTTGTACCCTT[A/G]TAACAATGCAGTCCT | 89910 |
rs550637209 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3B | GRCh38.p7 | 12:109480456 | AGTTTGAGACCACCA[A/G]CCTGGGCAATATAGC | 89910 |
rs550674530 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476699 | CTGGGCTCTCTCGAT[G/T]TCTTTCCCTCACTGG | 89910 |
rs550761138 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489284 | AATGACAATAATGTG[A/G]TAAGTGCTTGGAAGG | 89910 |
rs550782008 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525013 | ATTGTGTCCTGGTGG[A/G/T]GGTCCCTGCATGAGG | 89910 |
rs550817101 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537981 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 89910 |
rs550838359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109503319 | AGGGCATTTTTGAGC[C/T]GTTCCTCTTAGAGAT | 89910 |
rs550859444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109490307 | CCCTCAGATTCCTTC[C/T]TGGTTGATGTCTAGA | 89910 |
rs550865808 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109489803 | GGAAAAGGGAGGCAA[A/G]CCAGGGGGTATCTCA | 89910 |
rs550893322 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109505608 | GAAAGACTAGTTATG[A/C]GTGGGGCACCTATGT | 89910 |
rs550912698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109506387 | GAGTTTCGCTCTTGT[C/T]GCCCAGGCTAGAGTG | 89910 |
rs550974136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109513286 | TTTCTCTGTGGTTCA[C/T]GTGTGCTGTGGCCAC | 89910 |
rs550988619 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535837 | TTAAACTTCATTTCT[C/T]TTCCAACCCATTGTG | 89910 |
rs551027426 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | UBE3B | GRCh38.p7 | 12:109541566 | AGGGTGGAGTATTGG[C/G]TCAGAAGGTAACTCT | 89910 |
rs551049383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505695 | TCCTACCCTTGAAAA[C/T]GTGAGGTCTAAGCTC | 89910 |
rs551064206 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109540893 | CTCAGAGCCAGAGCA[G/T]GTGGTGAGGAGGTAT | 89910 |
rs551116324 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109543189 | ATACAGAAGGGCTGC[A/C/G]TGTGCGTGTGGCTTG | 89910 |
rs551131764 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109521610 | CGGTACCATGGGCTT[C/T]TTCACATACACATAT | 89910 |
rs551136436 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109525384 | GCTGTCTCGCAGGAT[C/T]GTTCTCTACAGAATA | 89910 |
rs551180133 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518350 | TCCATAACGCTCTTG[A/G]GTTTTTAAGAGAAGG | 89910 |
rs551183523 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541716 | GGCCAGAAGCCTGAA[A/G]TCAAGGTGCCCACAG | 89910 |
rs551190184 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542469 | TAATCCCGTCCTCAA[C/G]ATGGTGTATGGGTTG | 89910 |
rs551315736 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485339 | GGGCAAGATCTCTAC[A/G]CTCATGGAGCTCATA | 89910 |
rs551343401 | snp | A/C/T | 0.00398691 | 0.0444912 | intron-variant | UBE3B | GRCh38.p7 | 12:109519470 | TTTGAATCCAGTAAA[A/C/T]GCTCCTTGAGCTAGG | 89910 |
rs551361863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499368 | GGGATCATCATTCCA[A/G]TCTTACAAATGAAGA | 89910 |
rs551438517 | snp | A/G | 0.00368905 | 0.0427892 | intron-variant | UBE3B | GRCh38.p7 | 12:109489884 | GTCACATTATGGCAA[A/G]AGACTTTTTTGTTCT | 89910 |
rs551477905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515485 | AGCGATTCTCCTGCC[C/T]CAGCCTCCCGAGTAG | 89910 |
rs551566899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485628 | TGGCTGTGAGGCAAA[A/G]GTCAGTATCCATGGT | 89910 |
rs551590647 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477321 | AGGCAGGAAACACCC[A/G]GCTCACGCCAGCCGG | 89910 |
rs551623449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496706 | GAAATGTATGTTTAG[A/G]TCCTTCGTCTACTTT | 89910 |
rs551630142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109492045 | CGGATAAATATTTCA[A/G]CTCTATGGGCCATAC | 89910 |
rs551684416 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537289 | TCTCCCCACAGGACA[C/T]GCAGCCGTTCTCACT | 89910 |
rs551715435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109490372 | TTTCCACTTTGTACC[C/T]TGTTGTGCCAGATCA | 89910 |
rs551777565 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109531100 | TACACTCCTACTCAC[C/G]AGGGACTGTCTCTCT | 89910 |
rs551805595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542457 | AGATCATACTATTAA[C/T]CCCGTCCTCAAGATG | 89910 |
rs551827842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497412 | AGTTATTGGTGAGTT[A/G]CCACAGAGTGAACAC | 89910 |
rs551828185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525429 | TGTTCCTGGAATCAG[G/T]GGAAACCTCAGGCTG | 89910 |
rs551853600 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535916 | GGAACTGAGGCAGAG[A/G]CCCTGTTTGTGGTCT | 89910 |
rs551890082 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478441 | AATAGTAGCTGTTAA[-/T]ATGAATAGTCTCTTT | 89910 |
rs551944071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109504879 | GCGCAATCTCGGCTC[A/G]ACTGCAGGCTCCGCC | 89910 |
rs551953110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525996 | ACCTTTTTAGTAAAC[A/G]CACATTTTCATCATA | 89910 |
rs551980353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498003 | AGAAAGTAAAATGGC[C/T]TCTCTGCTTATTTCC | 89910 |
rs551981400 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540001 | TATAGACCTTCCACC[A/G]AGAGAGCCAGCCTGC | 89910 |
rs552036346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504227 | TTGGGATGTTTAGCA[A/G]CCCTGGTCCCTACTC | 89910 |
rs552143962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531704 | TCCCCACAGGTCTCC[G/T]GGGATTTAGGATGGG | 89910 |
rs552149631 | in-del | -/A | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536385 | ACTGTCAGCACAGGG[-/A]AGATGGATCCCATCC | 89910 |
rs552163748 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3B | GRCh38.p7 | 12:109516425 | CAGGTAATCCGCCCA[C/T]CTGGGCCTCCCAGAG | 89910 |
rs552167677 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109508862 | CTTACTAAGTACCTG[C/G]TAAGTGTCACTAGTA | 89910 |
rs552189154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517172 | CCTTTGAAATGAGGA[C/G]AGGAGCTGCCAGTCA | 89910 |
rs552288847 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109482480 | AGATGGCCCCTAGTT[A/C]TAGCCATCCGACTTT | 89910 |
rs552307109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109481870 | GTTTTTTTAAAAAAG[A/T]TGAAACCCACAATTA | 89910 |
rs552406939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539968 | CTTGGGCATACTGGG[A/G]TGGGGTCTGTGTCAG | 89910 |
rs552415231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109510706 | TTATATTTAGCATAC[A/G]TTTCTCATCCAAACT | 89910 |
rs552458676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475617 | GGGGGATTCGGATGT[A/G]GGACCAGGGCTTACT | 89910 |
rs552524891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109510278 | ACTGCGGAAGACAAG[A/G]GCTGTCCTCCCCTTG | 89910 |
rs552549233 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109529603 | AATGTCTCCTTGTGA[C/T]TCCCGACATAGTGGG | 89910 |
rs552570442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109495412 | AATTCACATCTCATA[C/T]ACTTTATTCATTTAA | 89910 |
rs552611161 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524937 | CTGGTCTCAGGGCCG[C/T]AGCACGTCTCCTCCC | 89910 |
rs552633407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502211 | CATGAAAAGGGGTCT[A/G]TGGATGCTTTCTTCT | 89910 |
rs552715717 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109529401 | TCCGCCTTGCCATAG[C/T]ATTAGACTGTTGATC | 89910 |
rs552742368 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523559 | GCTCCCCAACTCTGC[C/T]TTTGGGGGAGAGCTT | 89910 |
rs552760343 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494598 | TCAAGTAAGCAGTGC[A/G]CTTATAGACTTTGTC | 89910 |
rs552766612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109488058 | GTTCTTAGTGCATCA[C/T]ACGCATTAATCCATT | 89910 |
rs552771459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109540755 | CCCTCACACAGAGTC[C/T]TAAACTAGCCTGCCT | 89910 |
rs552777458 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493577 | AGGCTACTCTAAAGC[C/T]TTTTTCCCAAATAGA | 89910 |
rs552941303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109528806 | AGTGAGCCGAATCGC[A/G]CCATTGCACTCCAGC | 89910 |
rs553058449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109503619 | GCTTTCCTTTCCAAT[A/G]ATCATTTTACCATGT | 89910 |
rs553075528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517384 | GATACCACTGAAGTG[A/G]CCCACCTGAGCTAAA | 89910 |
rs553096680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109501691 | GAGTCTCACTGTATT[G/T]CCCAGGCTACAGTGC | 89910 |
rs553133233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109524571 | AGACCTGCCGTGTTA[C/T]TTGTTTTCCTCAGAA | 89910 |
rs553178742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494758 | AGTCTGGCCTCATGC[A/G]GACTAAAAAGATCAC | 89910 |
rs553201718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109530790 | GCACATCCTCTCCCA[C/T]AGGCAGGCCTCCCGG | 89910 |
rs553205157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109529548 | ATGAAAGTCCAAAAA[A/G]CACCCTTTGTACTAA | 89910 |
rs553337182 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523357 | TGTCCCTTCCCTGCT[C/T]AGAGCCCTCTGGACA | 89910 |
rs553347243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496202 | CTTTTTTCACTTTGC[A/G]TAATATAATCAGAGT | 89910 |
rs553351024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504357 | GTTGAAAGCCACTGG[C/T]CTAGTTTAGTAGCAA | 89910 |
rs553361313 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484266 | AGATAAAACATAATA[C/T]AAAATACAAATCATA | 89910 |
rs553476521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494234 | TAAACCCAGGCTATT[C/T]AACTCCAGAACTCAT | 89910 |
rs553672456 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516616 | ATGCTTCTGTTCTCA[C/G]AGGACACTTCTAACT | 89910 |
rs553673791 | in-del | -/GCTGTTAG | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109485237 | GTCTCCAAGTTACCA[-/GCTGTTAG]GCTGTTAGGCATTCC | 89910 |
rs553697254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109481987 | TCACTGTTGAGAAGG[G/T]GTCACAGAGGTCCCT | 89910 |
rs553708669 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109514902 | TCCACTCAGTACCAT[C/T]CCCTTTCTTCTTCTT | 89910 |
rs553858652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109527494 | AATCAGATGCACGTC[A/G]CAGTCCAGTGTTCCC | 89910 |
rs553919191 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510521 | GCACGCTGCCCGAGC[A/T]CTCAGCTCTCATGTT | 89910 |
rs554013265 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109520700 | AGCGGGAGATGAGGG[G/T]TGATGGGTAATTCTT | 89910 |
rs554047913 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109493336 | GCAGCTCTGCCTCCC[C/G]CTCCACCTCCAGAGA | 89910 |
rs554230274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505885 | CAGAGAGTGCCCTAT[A/G]AGATGAGAGGTATTG | 89910 |
rs554300410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109494966 | CTTTCCTTGCAAATG[C/T]GAAGTGACTGGTTGT | 89910 |
rs554311829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528805 | CAGTGAGCCGAATCG[C/T]GCCATTGCACTCCAG | 89910 |
rs554348419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109512758 | AGTGATGTGCAAACA[A/G]TGTGGCTGTTTAAAT | 89910 |
rs554355689 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503864 | CATGAAGGATTAAGA[A/G]CTTCTCTGCTGCATT | 89910 |
rs554377762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109480172 | GTAACTGTCCAGGTG[A/G]GAGCCTCTGCTGAAG | 89910 |
rs554411219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538170 | CAGAGTTTGAGAAGC[A/G]CTGGCCTCCACTCTT | 89910 |
rs554436416 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109532824 | GGCCTCATTTTTGTC[A/T]GTGTGCTGAGAGGTT | 89910 |
rs554450288 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109544064 | GTGTTTGGGAAGCAG[A/C]TGCCCACAGCTCTGG | 89910 |
rs554484024 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109501734 | ATAGCTTACTAGCCT[C/G]TAACTCCTAGGCTCA | 89910 |
rs554587775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515960 | CAGGTTGAAAGGTCA[A/G]GGAGCTTTATACTGT | 89910 |
rs554626494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523238 | TGCCGCTACCCTGGC[A/C]CAGTCTGTCGGCGTT | 89910 |
rs554848544 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109538735 | GATGGAGAGCAGTTA[C/T]CTGTTGCACTTAGGC | 89910 |
rs554859471 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109528235 | TCTTGCACTTTATGA[G/T]TGTTGGATGTTTCCC | 89910 |
rs554876573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528656 | ATCAGGAGTTGAAGA[C/G]CAGCCTAGTCAACAT | 89910 |
rs554896285 | snp | C/T | 0.001491 | 0.0272631 | intron-variant | UBE3B | GRCh38.p7 | 12:109533568 | GATCAGGTACCCCCA[C/T]GGGGTGGGTGGGGAA | 89910 |
rs554938099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526285 | GATGTTTGTGCTGGG[C/T]CCTCTCATCTCCGGG | 89910 |
rs555076610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109506646 | GTGAGCCACAGCACC[A/G]GGCTGCCAAATCTGT | 89910 |
rs555087852 | snp | C/T | 0.000349055 | 0.0132063 | intron-variant | UBE3B | GRCh38.p7 | 12:109498405 | CCATCAGGGAAAGCC[C/T]GAGTGTTTTGCCTGT | 89910 |
rs555124927 | snp | A/G | 1.73966e-05 | 0.00294924 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521547 | TGGGGAAGGCTGTGT[A/G]TGAGGTAGGAACGTT | 89910 |
rs555202272 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109526861 | GGGCGACAGAGTGAG[A/G]CTCCGTCTCAAAAAA | 89910 |
rs555222003 | snp | C/T | 4.94409e-05 | 0.00497172 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486509 | TTCTAAGGACCTCAC[C/T]CTCCTTTGGATTCAA | 89910 |
rs555285636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494026 | AGACAGGGTCTCACT[A/G]TATTGCCCAGGCTGG | 89910 |
rs555313890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485137 | CCAGTTTGCACCTTA[A/G]GGATTAGAATGATCA | 89910 |
rs555344807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109493440 | ACATATGATTCACCA[A/G]CATGCTCACATCCAG | 89910 |
rs555347084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109500709 | GGACTTGGACGACTT[G/T]CTTTGCCTTGCTTTC | 89910 |
rs555372385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478167 | AAATGGAGTAATTAG[C/T]AGGTTTCACAGAGGG | 89910 |
rs555374433 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477029 | CCCAAATGTGCTTCC[C/T]GGATTCCTAACCGCC | 89910 |
rs555374941 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109532232 | ACAGGACTAACCACA[G/T]CCCCGACACACAGCA | 89910 |
rs555383964 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513140 | TAGGCTCCAGCCTTC[A/G]TCTCCTGGGCCTCAT | 89910 |
rs555414168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109537134 | AGATTACTGGCATGA[A/G]CCACCATGCCCAGCC | 89910 |
rs555469855 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109537025 | GTAATATTCTTTTTT[C/T]GTTTTTTTGAGATGG | 89910 |
rs555496780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109518685 | GAGAGTGGCAGAATC[C/T]GACTCCCTTCACAAA | 89910 |
rs555521693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513818 | CTGCTCCGTGATTGC[A/G]GGTCCTGGGGGAGTA | 89910 |
rs555639642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505767 | AGAATTCCTTCAGTT[A/C]ACCCTCTAAGTATCC | 89910 |
rs555709234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486282 | CACAGGATAGTAAAT[G/T]TTCTTACTAGGCTAT | 89910 |
rs555715714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109521006 | AAAAGCAGGTGAGAA[C/T]GGCTCCTGTCATGCA | 89910 |
rs555815625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485800 | AAACATTTCTATAGG[C/G]TTCCTCCAGCTCTTG | 89910 |
rs555815951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525603 | AAATGATATGTCCTT[C/T]GATTTTTAGGTGATC | 89910 |
rs555841802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109483492 | TGTGTGTTTTTCACA[A/C]AACAATCTACAACAC | 89910 |
rs555856848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525106 | AGCCGACTTATTAGA[A/C]TCGCGCTTGGGCACC | 89910 |
rs555872086 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536729 | TTCTGCATTTCATTC[C/T]GCCATATGCCTGGAC | 89910 |
rs555878963 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109492317 | AAATGCTCAGCGGCC[A/G]CATGTAACTAGTAGC | 89910 |
rs555964783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109514835 | CGTCAGTCCTGTCAC[A/G]TCTAGATCTGTCAAC | 89910 |
rs556045196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542725 | ACTTCCAGCCATCAC[C/T]CATAGCCAGGAGAGA | 89910 |
rs556184657 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478985 | TCAGCTTTGGAAATA[C/T]AGAGGTAAGACAAGA | 89910 |
rs556230869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533154 | CTGCCTCTCGGGGAC[A/G]CCTCACCAGTGCCCT | 89910 |
rs556246915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532721 | GCCGGGAGTTCCCAG[C/G]GGGTAGCAGGGAAGT | 89910 |
rs556289279 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109491797 | TGCCTGCTCTGCCCC[C/T]ATCTGTGGATCTACA | 89910 |
rs556344294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526094 | CTCCGAAATGCCAAC[A/G]CATTCCCCTCCATGA | 89910 |
rs556372581 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477431 | TCCGTTGTGCGCCTA[A/G]GGGCCAGTTTTCTTT | 89910 |
rs556393125 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502193 | AAATGTTTCAGAAAC[C/T]GACATGAAAAGGGGT | 89910 |
rs556496211 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109506506 | GGTGCTGGCCACCAC[A/G]CCCGGCTGATTTTGT | 89910 |
rs556583501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109512401 | GGATGAGAGAGACTT[A/G]GGGAGGATTGGGCTG | 89910 |
rs556585094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109541987 | CTGTTTCCAAAAAAG[C/G]TCCCATGCACAGGTT | 89910 |
rs556618293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109519941 | TGAACATGGCAGGAA[A/G]GCAGCAAGGGTTCCC | 89910 |
rs556619380 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477083 | CCGCCCCTAATTCTC[C/T]ACCCAAAGCCCTTCC | 89910 |
rs556671750 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109516484 | GCCCAGCCTTGAGGA[-/G]GATTTTCTCGTGGGC | 89910 |
rs556785731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109537998 | GAGCCACCGCGCCCG[A/G]CCAACATTCTGGCTT | 89910 |
rs556808922 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536360 | TCGTGCATACATGCG[C/G]GGACCCCAGACTGTC | 89910 |
rs556842452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505809 | TGATGGAGTTCCCCC[A/G]ACTCCCACTGCTGGC | 89910 |
rs556845978 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536074 | CAACAAGAGCTGTCA[C/T]AGTGGCAGCAAAGCA | 89910 |
rs556846011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109542602 | TATAGGAGTAGGGTG[A/G]GACCCTAATCCGATG | 89910 |
rs556861326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109543308 | TGGAATAATCCACGG[A/G]CCTGTCACCAGGTGC | 89910 |
rs556884528 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109541282 | AGCAGTGACCCAGGC[C/T]GGTGACGGGCAATGT | 89910 |
rs556933777 | snp | A/C | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524067 | TAGCTCGGTGGATGA[A/C]CTGCCTTCTCTGGAC | 89910 |
rs556951279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497182 | AAACATAAAAAAGAA[A/G]AAAATTTCTCATAAT | 89910 |
rs556951575 | snp | C/T | 8.37542e-05 | 0.00647071 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483600 | TTCATCGATAGAGCC[C/T]GTCAGGCACGAGAAG | 89910 |
rs556990129 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519313 | AGGAACGCTGACTCA[-/C]ATTCACCTCCCAAGA | 89910 |
rs557037673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482124 | GCCTTTCAATAACAC[A/G]TAATTAATTTAATAC | 89910 |
rs557047411 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109511099 | CAGACTCTTGAGAAA[C/T]AGACAGCACCCTGCA | 89910 |
rs557117455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518333 | CATGTGACGAGGTGG[C/G]CTCCATAACGCTCTT | 89910 |
rs557130006 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109484116 | GTCCCTTTTGTTTTC[G/T]TGGGACCTGTTTTGG | 89910 |
rs557154574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517624 | ACAGCCTACCCATAC[A/G]TGCTCATCCTGCCAG | 89910 |
rs557155971 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109531269 | TGTCTGTAAAAGTTG[C/T]AAATGTTCAAAATAT | 89910 |
rs557193181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524653 | CCATCCTCCTCCCCT[C/G]TTGCCAGGAGGGAGG | 89910 |
rs557242227 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481810 | ATGGCTACCGTTTCT[C/T]TCCAAGCCTTTTATA | 89910 |
rs557273493 | snp | C/T | 0.000140795 | 0.00838916 | utr-variant-3-prime, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490610 | AGGAACCTTCTACTT[C/T]ATACCATAATTAAAC | 89910 |
rs557323111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109530126 | CTCCCAGAAAGCCAG[A/C]TGCTCCCTCGCTGGG | 89910 |
rs557336733 | snp | A/C/G/T | 6.71249e-05 | 0.00579301 | intron-variant | UBE3B | GRCh38.p7 | 12:109490046 | CAACTTCTCCACTCT[A/C/G/T]CAACACCTGCACTTG | 89910 |
rs557456064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536956 | TCACCCACTTCCCAG[A/T]GGCAGCTGTCACCAT | 89910 |
rs557489943 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494036 | TCACTATATTGCCCA[C/G]GCTGGTCTCAAACTC | 89910 |
rs557497964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109540228 | GTTTTTTGAGACAGG[A/G]TCTTGCTGTGTTGCC | 89910 |
rs557586007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532106 | CCCCGCTCGCAGGAG[C/T]GGGAAAGCTTCCCTC | 89910 |
rs557614886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497223 | GAGATACATTGTTAA[C/T]TTTATCTGTCCTCAA | 89910 |
rs557646178 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512632 | AAGAGCATAAATCAT[A/G]TTTTTGTAAATTAAA | 89910 |
rs557707482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490800 | TAAAAACACTGCATA[C/T]GGTTTTTTGTTTTTT | 89910 |
rs557775255 | snp | A/G | 8.375e-05 | 0.00647055 | intron-variant | UBE3B | GRCh38.p7 | 12:109486433 | AGTGATATGATCTCT[A/G]TAACAGCCCATGACA | 89910 |
rs557777133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109491407 | CTAAAAGAGGCCAAG[A/G]TGCAATCATTTTTCC | 89910 |
rs557796793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542677 | CAGAGGCAGAGACTC[A/C]AGTGGGGAACCTTCA | 89910 |
rs557798920 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541015 | ACGTCTCTGGCTCCA[C/G]CGTCCCCATGAACTG | 89910 |
rs557813966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109489064 | TCCCTGGTAAGTGTC[A/G]TTAGTGCCGTGTGTT | 89910 |
rs557849116 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514400 | GGTTGCCCAGCCCTT[A/G]CAGCCTGGATAAGCT | 89910 |
rs557871772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109489130 | GCCCATACATGCCAG[A/G]TGCCTCTAGGCGCTG | 89910 |
rs557889748 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517068 | GCTGCTTGGTTAAAC[A/T]TGTTCTCATTGCTGG | 89910 |
rs557890490 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109504684 | TTCAGCCTAGGGCAG[G/T]TTTCCCAAAGATGAG | 89910 |
rs557894439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109511720 | TAGGAACTAGAGCAA[A/G]ACAGCCTTAGAAACC | 89910 |
rs557913751 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109520082 | TGACAGTGTTACAGT[C/T]GTAGCTGAAAGGGAG | 89910 |
rs557919158 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109479550 | AGACTTTTTCTGCTG[C/T]GCACAGCCTTTTCTT | 89910 |
rs557922950 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510030 | AAGATAAAACATGTG[C/T]CAGTGCACACTTGAG | 89910 |
rs557950417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526156 | AAGGATTGGGTGAGA[A/G]AAAAACCTTTTGTAT | 89910 |
rs557950815 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489544 | AAAAATTGTTCAGTT[C/T]TGGGCCCTGCTGGGA | 89910 |
rs557960109 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481574 | CTCAGTGAGGAAGAT[A/G]TATGATACCACACCT | 89910 |
rs558017229 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477606 | TTTCCGGAACTGGAT[G/T]CTTGCTTCCTGGCGG | 89910 |
rs558092665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484360 | TGCCCCATCCACGGG[G/T]AGCAGCTACTACACA | 89910 |
rs558132559 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534446 | TGGGGCTTGACCTCG[G/T]GTAGTGGTGCCAGGG | 89910 |
rs558235590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109530277 | GCAGGCCTGAGGACT[C/G]GGGGTTCTCTGAAGC | 89910 |
rs558320336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495716 | GGGAAACAAAGGGAT[A/G]GGCCGAAATAAAGGG | 89910 |
rs558519514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539576 | ACCCACCATGCAGTC[C/T]TGCCGTGAACCACAG | 89910 |
rs558587738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109516588 | TTTCTAATTCCCACA[A/C]GTGTTCCAGGGAATG | 89910 |
rs558609897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109509150 | CCATTATCAGCTTCA[A/G]CAGTACCACCTCACA | 89910 |
rs558627823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502628 | GAACTAGAGGTTGTC[A/G]CGCCTTACTTCCCTC | 89910 |
rs558631820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494085 | CATGCCTCAGCCTCT[C/T]AAAAAGTGCTGGAAT | 89910 |
rs558651470 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3B | GRCh38.p7 | 12:109508116 | CTTGAGACACCCTGG[A/G]CAAGGGATCACGGAT | 89910 |
rs558657880 | snp | A/G | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109523869 | ACTTAGGAGGGGCCT[A/G]GAAATGCCGATGGCA | 89910 |
rs558670321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496139 | ATTTGCCTGTTGTGG[A/G]CATCTCACATAAATG | 89910 |
rs558724310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109516152 | ATGAGGAGGATTTTC[C/T]TTTTTCTTTTTTTTC | 89910 |
rs558730879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109503336 | TTCCTCTTAGAGATT[A/G]GTCCACCTCAGTTAC | 89910 |
rs558747324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109541109 | CTGCTGCATCCCTCA[A/G]ACCATGTTCCAGCGT | 89910 |
rs558780081 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523769 | CTGTAGCTCCAAACC[A/G]TGTGTCCTGACCACT | 89910 |
rs558818420 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109535026 | CAGATTCCACCAACA[C/T]GGGTCCATTCTTCCT | 89910 |
rs558821548 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109543405 | ACAGCAGGACTCGGC[C/T]GAGGCCCTAACGGTT | 89910 |
rs558844971 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540477 | TGGTCTCCCAAAGTT[-/C]TGGGATTACAGGCAT | 89910 |
rs558860537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109523310 | TCCTGTCTTCCTCTC[A/G]CCAGCCCATTCCCCA | 89910 |
rs558901034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528799 | AGGTTGCAGTGAGCC[A/G]AATCGCGCCATTGCA | 89910 |
rs559053982 | in-del | -/TC | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109484773 | TTCATTCTTTCATAT[-/TC]TGAGACAGGGTCTCA | 89910 |
rs559129517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534483 | CCTGCACTCTGCCCA[G/T]CATCCAGGGACTGGC | 89910 |
rs559155276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528307 | CTCACCTCCTCCCTT[C/T]CTCTCCCCCTTTCTC | 89910 |
rs559162274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109481056 | CTTGCAGTGAGCCAA[C/T]ATCGCGCCACTGCAC | 89910 |
rs559171754 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109539822 | TGTGCCCACACCCCA[C/G]CTATTCCCGAGCTTC | 89910 |
rs559187494 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517956 | CTGGTGATCAATGCC[A/G]AGAGCTGCTAGGAAG | 89910 |
rs559270192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487446 | ACCCCAGTAATAATC[C/T]ATTCCCAGCCATCCC | 89910 |
rs559307398 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534370 | TTACTTAGTGCAGGA[A/G]TTCTCTGTGCAGGCC | 89910 |
rs559361366 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508811 | GCTCATTTATTCATA[C/T]GTTCTTTCAAACATT | 89910 |
rs559392312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527744 | AGGGCCAGAGAGAGA[A/G]CATGGTGAGTCCTGC | 89910 |
rs559429046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533363 | TAGACAGCAGTTACA[A/G]CACGGTAACAGACAG | 89910 |
rs559461653 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539969 | TTGGGCATACTGGGA[C/T]GGGGTCTGTGTCAGC | 89910 |
rs559482791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522802 | GCCCTCCAGTGATTT[A/G]GGTCCTGGGCCCATT | 89910 |
rs559522182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109501918 | ATCCTCCTACCTCAG[C/T]CTCCCAAAGTGCTGG | 89910 |
rs559605469 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535198 | CAAAGCCTACTGTGC[A/G]TGAGATCCTCTCCTT | 89910 |
rs559621921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524357 | TTCCCAGCACCAAAG[C/T]AGCGCCTCAAGGGAG | 89910 |
rs559635527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486669 | GTATTTTCAGAGTCA[C/T]TATCAACGAGAGTTG | 89910 |
rs559712171 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109506945 | CCGAGGTGTAACCAG[G/T]CAAGCTGTCTCTGTA | 89910 |
rs559728881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522173 | GGGTTGCCGTTAATG[A/G]TAAGTGAGGAGGGCC | 89910 |
rs559753334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515473 | CTCCCAAGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 89910 |
rs559769389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109533789 | CCTTTCTCTTTCCTT[C/T]CTCAGGGAAGGGTAC | 89910 |
rs559779646 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109487061 | TTTTGGGGTCACCTC[A/G]TCCTTTCCTGCTGTA | 89910 |
rs559822978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478505 | GATTATTGAGGCTGG[C/T]CACGGTGGCTCACGC | 89910 |
rs559891959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109509319 | TGCAGGTTTGTTACA[C/T]AGGTATACATGTGCT | 89910 |
rs559902667 | in-del | -/TGTT | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109482372 | TATCTTATTCCACTC[-/TGTT]TGTCCATGTGGGCCC | 89910 |
rs560046487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499407 | TGAGACATGGGTTGA[C/T]GGCCACGGCTCACCT | 89910 |
rs560071565 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532068 | AGCAGAGCATCCAGG[A/G]GTTTCCTGTGTCCTC | 89910 |
rs560149761 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109513287 | TTCTCTGTGGTTCAC[A/G/T]TGTGCTGTGGCCACT | 89910 |
rs560248561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498481 | TTACAATAAAAAACA[A/C]GTATTTAGATAGACA | 89910 |
rs560316646 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109492829 | AATGTTATTTTTACA[G/T]GTAATCAATATTTTT | 89910 |
rs560323882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109543446 | TTAATTGTGGGAGAG[C/T]GTCTAGAGTGAAGGA | 89910 |
rs560455044 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491100 | TATCCAAAGGCACTT[C/T]AACAGCAGCTTTTTC | 89910 |
rs560457462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484669 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTACC | 89910 |
rs560537089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109500247 | GGAATATAAATTTTT[A/G]AAAGTGTAATTATGA | 89910 |
rs560602660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505509 | CTCCACAGTGTTAAC[C/T]GTTTCCTCTGTTTCT | 89910 |
rs560670744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109491824 | TACAGTACACCTTCA[C/T]GCTGAGAGCTCTGAG | 89910 |
rs560729072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520524 | GGTCTCTGCTCCCTG[A/C]GTTGATCCCTGCCAT | 89910 |
rs560776412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531772 | TCAGTTCAGTTTTCC[A/C]AGAAGTGCCTCATGG | 89910 |
rs560781931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109514996 | TCAGCTCACTGCAAG[C/G]TCCACCTACCGGGTT | 89910 |
rs560782394 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109487980 | ACTTGGTGAAACAAT[-/G]AACTGTCATCAAAAT | 89910 |
rs560874792 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109487162 | ACCAGTTCAAAAATC[C/T]AGGTTTCTTGTAGGT | 89910 |
rs560878345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109493783 | ATTGTTCTAAAACTT[C/T]TACACGTATTAACTG | 89910 |
rs561068194 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543653 | GCCTGGCCAACATGG[C/T]GAAACCTCGTCTCTA | 89910 |
rs561108077 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493975 | GGACTACAGGCACAT[A/G]CCCAGCTAATTTTTT | 89910 |
rs561108808 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3B | GRCh38.p7 | 12:109531349 | AAGTATTTCCTAGGA[C/T]GCTGAATGGCACACA | 89910 |
rs561150587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109539343 | GCATCCTTTGCTTCA[C/T]GGCAGTCATCCTGAC | 89910 |
rs561189167 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109538990 | CCTGTAATCTGAACA[C/T]TTTGGGAGGCTGAGG | 89910 |
rs561285335 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499237 | AAAGACCATTTCTTA[A/T]GTTAACCCTTGATTT | 89910 |
rs561285343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109491883 | GGGCTTATTTAACCC[A/G]GGGTTGGCCCAAACG | 89910 |
rs561343015 | snp | C/T | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109519352 | TATAATCCTCGCATA[C/T]CCACGCCAGTTCCCA | 89910 |
rs561381534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532405 | TTAAAACTTTTTTTG[A/G]TGCCCGACACACATA | 89910 |
rs561416428 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109537449 | GGCCTGGGAAGCCCC[A/T]GAGGATCAGAGCACA | 89910 |
rs561420611 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109525376 | GAAAGAATGCTGTCT[C/T]GCAGGATCGTTCTCT | 89910 |
rs561434311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532858 | AGTCTCTTGCACAGG[G/T]TCCCCCGGGGCCCCA | 89910 |
rs561465055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109521844 | TTCGTTGCTAGTTAA[A/G]TGGTAGAGGTGGAAT | 89910 |
rs561485973 | snp | C/T | | | missense | UBE3B | GRCh38.p7 | 12:109543603 | CAACACTTTCGGAGG[C/T]AGATGGATGACTTGA | 89910 |
rs561500228 | snp | A/G | 8.23771e-05 | 0.0064173 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521171 | CGAGCAGCTTAGGCA[A/G]CTCTCCCAGCACGCC | 89910 |
rs561504311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109543052 | TGCCCAGGCTAGATA[C/T]CATGTGGCCAGGCTC | 89910 |
rs561539818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527091 | GCAGATCATTTTGGA[C/T]GATAGCACGTGGCAG | 89910 |
rs561565830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527538 | CTCTCGGATCAGGTG[G/T]TTCAGTCAGTCTGCA | 89910 |
rs561716194 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482092 | TTAATACTAATAATA[A/G]AGCACACTTATTAAA | 89910 |
rs561735436 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507971 | GGAAGCTGATCAGTA[C/T]CACTGGCTGTGGCTT | 89910 |
rs561741092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109503752 | TCTGTGAGCACAGAA[C/T]TGGGTATCACAGGCT | 89910 |
rs561743867 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476576 | TGGAAGTTACAGATA[C/G]GTACCCAGGCGCCAG | 89910 |
rs561832848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109530922 | TTGTGCTCGGCACTC[C/T]GTCCTCCCCTTTGCC | 89910 |
rs561845491 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535440 | CCTCCCATTTTCTGC[A/G]TCCTCAGCGGGCTGA | 89910 |
rs561849956 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534424 | TGGAAGCCAGTCGTC[G/T]TGTGTCTGGGGCTTG | 89910 |
rs561861822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109483790 | GTTTTTTCTCATAAA[A/G]TGCTTGAAAAGCCTT | 89910 |
rs561907019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109482538 | TGCTACTTCAAGTAA[A/G]GTAGCCTGGTAGAGA | 89910 |
rs561923162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505537 | TCTATTTTAACCTAT[G/T]TTTGAATTGTGAGAG | 89910 |
rs561977112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109512123 | GGAAGCCATTGGAAA[C/G]GGGGTCTGGCATTCA | 89910 |
rs562000536 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529869 | TAATTGTCATTGTTA[C/T]CTCTTCCTTGTTGGC | 89910 |
rs562074019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504773 | GAGCAGCATCTTGAG[C/T]GAGAGGAGTTTGGGG | 89910 |
rs562119269 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109510542 | CTCTCATGTTCTAGG[A/G]CAGAGAGGACTTTTT | 89910 |
rs562130992 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477810 | CGGTCCGGCCTGCGG[C/G]AGAACTGGGTCGTCA | 89910 |
rs562161188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109489755 | GAGTTCCAGGTACGC[A/C]TTGCCTTTCTGTGCT | 89910 |
rs562169889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517859 | GCTGTTCCTCCTCAC[A/G]TGTCTTCATTTTCTC | 89910 |
rs562290450 | snp | A/G | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499756 | CTCAGAAGAAGTCCA[A/G]CCTGACCCACTGGCA | 89910 |
rs562350562 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536206 | TGATGGAAACATGGC[A/T]AGGAATTTAAAGACA | 89910 |
rs562374627 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496900 | AAGAAGCACAACTTA[C/T]CTGTTTTTTTCTTTT | 89910 |
rs562424196 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477791 | GGTAGGCCGGTAGGG[C/T]CTGCGGTCCGGCCTG | 89910 |
rs562480545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513942 | CCTCTGCCATTGAAA[C/T]ATTCTTGCTGGAGTA | 89910 |
rs562489456 | snp | A/G | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507684 | CTGAAGAGTCCAAGC[A/G]ACTCTTGGCCATGCT | 89910 |
rs562532233 | snp | A/C | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109499315 | TACCTCTGTGTGCCT[A/C]ACATTTTACCTGCCA | 89910 |
rs562695131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484558 | CACCACGCCCAGCTA[A/G]TTTTTGTATTTTTAG | 89910 |
rs562716290 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486760 | CTTTGGTGTGTGTTG[A/G]ACCCTTAAACTGCTT | 89910 |
rs562726995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498804 | TCCTTGCCTAAATTT[A/G]TTTTAGATAGGAAAA | 89910 |
rs562756062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490970 | TGAAGCACTCAGTTT[A/T]CTTTTTTGCTCTTTT | 89910 |
rs562838379 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109506226 | TTTGCCAAAGGTGGC[A/G]AGCCTGCAAGATGGT | 89910 |
rs562869226 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109490326 | TTGATGTCTAGAATC[A/G]TATTTCTAGCTCTGT | 89910 |
rs562891425 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109497364 | ATCTATAGTGTATAT[A/G]TAGTTTTAAATAAAC | 89910 |
rs562914383 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109542223 | CTGCCTCCTCCTCAC[C/T]CATGGCAGACATTAC | 89910 |
rs562972327 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535639 | TTATTTGTCTCACTG[C/G]TTATCTAATGAGGAA | 89910 |
rs563002842 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518145 | AATCTCCACTTCTGC[A/G]CCCTCCTGTTCTTGA | 89910 |
rs563020909 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109515103 | TATTTTTAGTGGAGA[C/T]GGGGTTTCACCGTGT | 89910 |
rs563049252 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109540715 | AGAAGCTATTGTGAA[C/G]TCATTCTGGCCCTTC | 89910 |
rs563063288 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513876 | TGGGCTGTCTTGTTG[C/T]CCCTCCGCCCATCTC | 89910 |
rs563087791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525972 | TTGTTACATCAGTGG[A/C]CTTTTTTCACCTTTT | 89910 |
rs563088555 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527161 | TTCAAATGCCACAGA[C/T]GGAGGTCCTTAGACA | 89910 |
rs563094201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482406 | ATTGTTTTGCTCCCA[C/T]TTCTAAGTGAGGTCA | 89910 |
rs563124554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531546 | AATCTCATGTGGCCT[C/T]ATCTGTTGAGGCAAC | 89910 |
rs563163856 | snp | A/T | 1.64727e-05 | 0.00286986 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530002 | CCCGAGTGGATCCGA[A/T]TGTTCTCAACTCCTG | 89910 |
rs563200724 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539711 | TTCTGGAGTTTGTTT[C/T]TGAAACTCCTTGCAA | 89910 |
rs563211637 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487103 | GAGCAGTTTTGACTT[C/T]ATATTCTTACTCTGT | 89910 |
rs563225726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109489518 | TGACCCTGGCCTCTT[A/G]GGGGGAACCCAAAAA | 89910 |
rs563286553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496284 | ATATTCCATTATATG[A/G]ATATACCACATTTGA | 89910 |
rs563303676 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476229 | GGACCAGAGTTTGAG[A/G]ACCACTGGTTTATGC | 89910 |
rs563362575 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109537584 | GTCCTCACAAGGAGC[A/G]TTCATGTAACTAAAA | 89910 |
rs563398823 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109495769 | CAGCAGGAGCAAGTC[C/G]TTAAGGCACAGATTG | 89910 |
rs563448395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109510658 | TGTTTACACCAAATA[C/T]GATTAGAGTTAATTA | 89910 |
rs563471115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518767 | TTTTTAAAGCATATC[C/T]CTCAGGGATGGCAAA | 89910 |
rs563478698 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482831 | AGGACCAGTTCTACA[A/G]TAAAGTCTTCACTGG | 89910 |
rs563511857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517942 | AGTGCCCCTGGCCAC[G/T]GGTGATCAATGCCGA | 89910 |
rs563571825 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109524814 | GTTACAAATGGAGGA[G/T]TATGTCTTAGAGAAG | 89910 |
rs563613701 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109479924 | ATGGACCCTCTGCCA[C/T]TGAGGCACTGTCTGC | 89910 |
rs563639799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528444 | AAAATTTTTTTAAAT[A/G]GGGATATTTTTGAGA | 89910 |
rs563733196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109502035 | CAAAACAAAAAATCC[A/G]TAAGAATAGAAAACA | 89910 |
rs563769031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109530882 | GGCTGCAGGGACAGG[C/T]CCCCTGCACAGGTGG | 89910 |
rs563775465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528946 | GGCAGATCACCCGAG[A/G]TCAGGAGTTTGAGAC | 89910 |
rs563779556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109481610 | ATTTAACCCTAAGTC[G/T]GGATTTTTTTCTTCT | 89910 |
rs563805012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109530462 | CTGCCAGAGTGGACC[A/G]TGCCAGCTGTCTGCA | 89910 |
rs563814925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534399 | CCCCAGGGAGAAGGG[G/T]TTCCTTCTCTGGAAG | 89910 |
rs563842166 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535746 | GGTCTTGCTGCCCAT[C/G]CTTCCTCAGCACAGG | 89910 |
rs563897934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502883 | ATTTATCCCAAAGAA[A/G]TGCCTTGAATTGAGT | 89910 |
rs563956547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524906 | AGCATACAGAGCAGA[G/T]CAGGGAGCAGAGACC | 89910 |
rs564103367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525259 | CTGGGCAGGCTGGCA[C/G]GTGAAGGCTCTGAGA | 89910 |
rs564194252 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109516427 | GGTAATCCGCCCACC[G/T]GGGCCTCCCAGAGTG | 89910 |
rs564255012 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109489647 | AAAGGTGCTACAGGC[A/G]CTCAGAGGCCAGAGA | 89910 |
rs564290509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109511438 | GGAAACGGTGGTTGC[G/T]ATTACTTTGGTGAGG | 89910 |
rs564359213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109518890 | GTCGTAATCTGGTGG[C/T]TTGGTTATTAGAATA | 89910 |
rs564411762 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508875 | TGCTAAGTGTCACTA[C/G]TATGTGTCTTAGATA | 89910 |
rs564475277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502970 | CCTTTTCCAGGGTGG[A/G]ATTTGGCAGCTGGCT | 89910 |
rs564520180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109516964 | GTGGACGGTCTCTGG[C/T]TTTTGAACTGTTCCT | 89910 |
rs564548718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495873 | CCTCATTCCAGTAGA[C/T]CTACAACCTTCTGGC | 89910 |
rs564556331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524228 | TTGCTGTAGCTGCTA[C/T]AGGCCCCTCACATCC | 89910 |
rs564602816 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109540773 | AACTAGCCTGCCTTA[C/T]GCTGGGGAGGGACAA | 89910 |
rs564802468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109490333 | CTAGAATCATATTTC[C/T]AGCTCTGTGTCCTCA | 89910 |
rs564823379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487743 | CAGACGTCAGGAGAA[A/G]AAGGGCCCTGACTCT | 89910 |
rs564884456 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487243 | GGGGTACTGCCACTA[G/T]CCCAGCCTGGTCCTG | 89910 |
rs564911605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539420 | AGATCTTACGAGGGC[A/G]TTAGAGAGAGCAAGA | 89910 |
rs564922910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523670 | CCTCTTAACTGAGAG[A/G]CTGGTGCTGCCCCCC | 89910 |
rs564964589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533305 | ATGTACGGCGTGTGC[C/T]AGTTTTGGGGCCAGA | 89910 |
rs565001996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533026 | GCACCACGTGCAGTG[G/T]GTGCCACCAGCCTCC | 89910 |
rs565008717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109508527 | TTCCACCTTTTCCCA[A/G]AAGGTTGGTGAAGAA | 89910 |
rs565019396 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537290 | CTCCCCACAGGACAC[A/G]CAGCCGTTCTCACTG | 89910 |
rs565110650 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520732 | TCATTTTACAGTGTT[C/G]TGTAGGTTTGATTTT | 89910 |
rs565231353 | snp | C/T | 0.000441846 | 0.0148569 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486570 | GATTTTCTCAAGCAG[C/T]TCAAGGTAACAAAAA | 89910 |
rs565232192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495131 | AGCTCAGTTGGTTAG[A/C]CTCACCTAGACAAGT | 89910 |
rs565236663 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478715 | GAACCTGGGAGGCGG[A/C]GGTTGCAGTGAGCAG | 89910 |
rs565293860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109493572 | AGGCCAGGCTACTCT[A/G]AAGCCTTTTTCCCAA | 89910 |
rs565295701 | snp | A/G | 8.20715e-05 | 0.00640539 | intron-variant | UBE3B | GRCh38.p7 | 12:109486082 | CTAAGGTAAGTGGAC[A/G]GGAGCCGCAGTGTCT | 89910 |
rs565296787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109480970 | CTTCTAAGGCATAAA[C/T]GTTTTTCCATTATCA | 89910 |
rs565310422 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476021 | GAATCACACCTATAA[A/G]AGCCCTCTGACTCCC | 89910 |
rs565342247 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541487 | CACATCTGTTAAGCA[C/T]CTGGCAAATTATAGT | 89910 |
rs565361817 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540105 | AGAGGAAGCTGAAAG[C/T]GTTCATTCTGCTGCC | 89910 |
rs565392269 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109522073 | TGTTCCTAGTCAGCC[A/G]TGTGACCATGTGCCT | 89910 |
rs565425762 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518217 | GCCCCCACGAGTGAG[C/T]TGATAAATGGCAACT | 89910 |
rs565455490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515422 | TTGCCCAGGCTGGAG[C/T]GTGATGGTACGATCT | 89910 |
rs565481454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479267 | CTTAAGGACAATACA[A/G]TAAAGCTCACTTACA | 89910 |
rs565484467 | snp | A/C | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510163 | TTTTGTCTGAGAGGT[A/C]CTCAGGCCCTGCAGA | 89910 |
rs565509574 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109517830 | CCCCCACCAGCAGAT[A/G]GCTTCTGGCAGCAGC | 89910 |
rs565662049 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503544 | CAAAAACAGTCAACT[A/G]TGCCTGAGTGTACTG | 89910 |
rs565666346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486864 | GATCTACATTATTAT[A/G]CTAGTCAGGCCTCTT | 89910 |
rs565691305 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109487297 | TCTGAAAAGGATGGA[A/C]AGGGGTGTGAGCAGA | 89910 |
rs565691993 | snp | C/G | 8.24681e-05 | 0.00642085 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516771 | TCATTTTAGAGAGTT[C/G]TACTGTTTCGAACCA | 89910 |
rs565724391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528627 | GGGAGGCCAAGGCAG[A/G]TGGATCACCTGAGAT | 89910 |
rs565947190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109486175 | ATTCACACACAAATG[C/T]AAATAAGTAGTGGAT | 89910 |
rs565948808 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536373 | CGGGGACCCCAGACT[A/G]TCAGCACAGGGAAGA | 89910 |
rs565951704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109523763 | TGAGCACTGTAGCTC[C/T]AAACCATGTGTCCTG | 89910 |
rs565972792 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109514734 | CTTCATTCCTATCAC[C/T]AGCCTCCCTCCCTGT | 89910 |
rs566045796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109483397 | CGGAGAGCTGTTAGC[A/G]CTTTGGAGGGTGTTG | 89910 |
rs566058920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109507288 | TTCCTCCTGTATAAG[A/G]TGGGGATAACACTGG | 89910 |
rs566060187 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109515108 | TTAGTGGAGACGGGG[A/T]TTCACCGTGTTAGCC | 89910 |
rs566097932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539129 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCTGG | 89910 |
rs566126428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498986 | GCACACTACCACGGC[C/T]GACTAATTTTTGTAT | 89910 |
rs566133476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109493918 | GCAGCCTCAAACTCC[C/T]GGGCTCAAGCCATCC | 89910 |
rs566138918 | snp | A/G | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498300 | TAAGAGACCAAGATC[A/G]ATGCCGTGATGTATG | 89910 |
rs566174579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109520750 | TAGGTTTGATTTTTT[C/T]TTTTTTTCTTTTTTC | 89910 |
rs566181829 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528031 | GCGCCCAGAGGAGGT[A/T]GGTGGGAGCAGGCTG | 89910 |
rs566226197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478765 | CAGCCTGGGCAACAA[A/T]GTGAGACTCCGTCTC | 89910 |
rs566306303 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543890 | GCCAGAGATGGTACC[A/G]TAAGGAGGGTTGGAG | 89910 |
rs566344353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109508001 | TGGGGTCTCCTGGAG[A/T]TGGGTTTAGATCATG | 89910 |
rs566374091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109533056 | CGCCTCGCCCTCACC[A/G]TCTCCCATTTTCTCC | 89910 |
rs566412653 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3B | GRCh38.p7 | 12:109532682 | CATTTGCAGGAATAA[C/T]GCAGGGGCTGCCGCT | 89910 |
rs566424790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109537070 | ACCCAGACCAGTCGC[A/G]AACTCAGGGGCTCAA | 89910 |
rs566459228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109491498 | CAGGGTGAGAGGATT[A/G]AGGAAATAATGTGAA | 89910 |
rs566619321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486160 | TGAATATTAGGACCA[A/G]TTCACACACAAATGC | 89910 |
rs566771767 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109490405 | CCTCTAGGGAATTGT[A/T]GAGAAAGCCTGATTG | 89910 |
rs566811242 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477325 | AGGAAACACCCAGCT[C/T]ACGCCAGCCGGGGGC | 89910 |
rs566871640 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476897 | CACCCCCAAATGTCC[A/G]TTTTCAATTGATATC | 89910 |
rs566884845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497514 | CCCCATCACAAACTC[C/T]TTCCTCTTCCATGTA | 89910 |
rs566903099 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540098 | ATCCTGCAGAGGAAG[C/T]TGAAAGCGTTCATTC | 89910 |
rs566954469 | snp | A/C | 9.96562e-05 | 0.0070582 | intron-variant | UBE3B | GRCh38.p7 | 12:109530699 | CATGCATGTATTCTC[A/C]TAAACCTGGAAGGCC | 89910 |
rs566985579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109519687 | AATTTAGGCAGAATG[G/T]TTTAAATGCTGTTAC | 89910 |
rs566986756 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109489978 | ATGGGACATCTCAAC[C/G]AGCATGGATTTTATT | 89910 |
rs566988150 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109499070 | TCGAACAATCCACAC[A/G]CCTCAGCCTGCGAGA | 89910 |
rs567041329 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493919 | CAGCCTCAAACTCCC[A/G]GGCTCAAGCCATCCT | 89910 |
rs567046548 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109492025 | CCAAATTTTCTGGAA[A/G]GAGCCGGATAAATAT | 89910 |
rs567065618 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525367 | TGAAGGAAGGAAAGA[A/G]TGCTGTCTCGCAGGA | 89910 |
rs567121801 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518993 | CCTGGGCATTGTTTC[C/G]TTTTTTATGGTTAGT | 89910 |
rs567123321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109519130 | GAAGGATCCTCAAAC[A/G]TACTCTTACCCAGTC | 89910 |
rs567130296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495019 | ATTTGCTTTTCTTCT[A/G]TTTAGGGAATTGTGC | 89910 |
rs567312559 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539713 | CTGGAGTTTGTTTTT[A/G]AAACTCCTTGCAAGA | 89910 |
rs567336990 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477041 | TCCCGGATTCCTAAC[C/G]GCCAGGGAGCCTCCC | 89910 |
rs567385679 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543920 | GCGGGCCTCTCAAAG[C/T]AAGCCTAGCAGTGTA | 89910 |
rs567395493 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493496 | TTTAAGAATATAACC[A/G]GCAGTCATCCTTGTA | 89910 |
rs567405672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109479585 | TCTCCATGGCATTTA[A/G]CAAAATAAGTACTTA | 89910 |
rs567422741 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE3B | GRCh38.p7 | 12:109538516 | GTCCCCTCCAGAGCA[C/T]GTGAGGATTAAATGC | 89910 |
rs567570072 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109484905 | GGGACTGCAGGTGTG[C/T]GCCACCATGCACAGC | 89910 |
rs567613517 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488183 | AAGCTCACACAGCTA[C/G]TAAGTGGTGAAGTCA | 89910 |
rs567675119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536814 | GAAGATGTGGAGGGG[C/T]GCAGAGCACATGTCC | 89910 |
rs567710342 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109526042 | ACAGTATTCCAGGGT[A/G]TGGATGTACCAGTGT | 89910 |
rs567748461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525621 | TTTTTAGGTGATCCA[C/T]GGAAGTGTTCTTGAA | 89910 |
rs567769188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531195 | CAATTGCTTAGGCTG[A/T]TATCAAGATGTATTT | 89910 |
rs567778412 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109521668 | CACTAGGATACAAGC[A/G]AGGACAGGGGCAGGA | 89910 |
rs567783657 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518511 | AAAAAGCCCAATTGT[A/G]TGGTAGGGACTCCCT | 89910 |
rs567792335 | snp | C/T | 3.31972e-05 | 0.004074 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491176 | GTTCTTGAATGCTTC[C/T]TCCTCTTGGTTTTTC | 89910 |
rs567799927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513407 | ATGAGATTGCACTAC[A/G]TTCTTTTTAATGATG | 89910 |
rs567818590 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512801 | TGGCAAACTCTCAGA[A/G]GTGAAGGGCCTTACG | 89910 |
rs567825672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109524943 | TCAGGGCCGCAGCAC[A/G]TCTCCTCCCACGGTT | 89910 |
rs567971584 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109519839 | GTGACTTAGGGGTCT[C/T]GAGAGGTAATTTTCC | 89910 |
rs567989143 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477976 | TCTTTTCACTTTGGG[A/G]ACGGTAGGCCTTTAT | 89910 |
rs568009398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542553 | TTATTTGGAAATAGG[G/T]TTGTTGTAGATGTAA | 89910 |
rs568031076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109541899 | TTAGAAGGACTTGTC[A/C]TTGAATTAGGACCCA | 89910 |
rs568038787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504362 | AAGCCACTGGCCTAG[A/T]TTAGTAGCAATGGAG | 89910 |
rs568088224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109511054 | TGCCATAGGCTATAC[A/G]TGTATGAATGAGTAT | 89910 |
rs568104365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109495969 | GGGGCCAGTTTATGG[C/T]CAGATTTTGGGGGCC | 89910 |
rs568119249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109518271 | AGCAGTTGGAAGCAC[A/G]TGCCTCCCCAGAAGA | 89910 |
rs568120373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495480 | TTGTGCAACCATCAC[C/T]TGCTGAGACCAGCTT | 89910 |
rs568182660 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109502398 | CGTTGCACGCTCTTA[C/T]TAAAAGTTATGGAAA | 89910 |
rs568200709 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475759 | GAGGCTTGTATAAAA[A/C]CTTCCCAAACTGAGG | 89910 |
rs568205941 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536330 | TCTGAACGTGTGTGC[A/G]CACGCTGGGCGGGTT | 89910 |
rs568227696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505293 | ACACACATCTGATAG[C/T]ACTGGCACTGCTGCT | 89910 |
rs568230513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504931 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 89910 |
rs568316605 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531075 | CTCCAGTATGGAATT[A/G]TCAACTCTCTACACT | 89910 |
rs568325097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496903 | AAGCACAACTTACCT[G/T]TTTTTTTCTTTTGAC | 89910 |
rs568356409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109488198 | GTAAGTGGTGAAGTC[A/T]GAAGGCTGAGCCCAG | 89910 |
rs568362592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524596 | TCAGAAAGAGCCCCA[A/G]GCTGAGGCTCTGTCT | 89910 |
rs568416862 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109489810 | GAGGCAAGCCAGGGG[-/T]GTATCTCATTTCTTA | 89910 |
rs568513965 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109483275 | CTTATCCTATGCCAG[A/G]TGCTGTGCTCTTTCC | 89910 |
rs568526741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109512187 | ATCTCCTGACTGCCC[C/T]CATGGACTGGGTGAG | 89910 |
rs568609560 | snp | C/T | 8.26576e-05 | 0.00642822 | intron-variant | UBE3B | GRCh38.p7 | 12:109530509 | CCATAAGTGCCCACG[C/T]TAGCACATTGCTGAG | 89910 |
rs568749634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109537503 | CAGGAAAGAACCCTG[G/T]AGAGGCTTGTGGCCT | 89910 |
rs568753755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531902 | AGGTGTGTTTGTGCC[G/T]TTGGATAACCTGTCA | 89910 |
rs568758926 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535408 | CTGCCTTGAAGCCAC[A/G]CGCTCCACGCCGCGG | 89910 |
rs568759308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505673 | AGGCTTCTTTATAAC[C/G]ACATCCTCCTACCCT | 89910 |
rs568764872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109488810 | AGGATGCCCTTGGTG[C/T]TGACCATCAGACTGC | 89910 |
rs568787520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109542614 | GTGGGACCCTAATCC[G/T]ATGTGACTGGTGTCC | 89910 |
rs568788272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536929 | TGAGCACCCTCTATG[G/T]GCCCATCCCTCTCAC | 89910 |
rs568832327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497684 | CCAGTGTATGTCCCC[A/C]ATTTCAGCCTTCAGT | 89910 |
rs568844763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505010 | GAGACGGGGTTTCAC[A/T]GTGTTAGCCAGGATG | 89910 |
rs568901074 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109489811 | GAGGCAAGCCAGGGG[G/T]TATCTCATTTCTTAG | 89910 |
rs568913183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496638 | TCCCTGGTAGTTAGT[C/G]ATGTTGAACATCTTT | 89910 |
rs568933103 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109489082 | AGTGCCGTGTGTTTC[A/G]TATGGTCATTTCATT | 89910 |
rs569045443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496077 | ACTCCCTTTTCCCCT[C/T]TCCCCAGAACCCCTG | 89910 |
rs569089545 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528393 | AATGATAGGAAAATC[-/G]TATTTGTATGTATTA | 89910 |
rs569124778 | snp | C/G/T | 5.11752e-05 | 0.0050582 | intron-variant | UBE3B | GRCh38.p7 | 12:109484003 | CGATAATAGCAAACA[C/G/T]GTATAATACTTCCAT | 89910 |
rs569137101 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489288 | ACAATAATGTGGTAA[G/T]TGCTTGGAAGGAAGC | 89910 |
rs569200278 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484213 | GATGCATGCAAGAGT[C/T]AGGAAGTTTAGGTAA | 89910 |
rs569306071 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476800 | TCCAAAACGCCAAAC[G/T]CTCCGCCCCAAGGAA | 89910 |
rs569351705 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478898 | GGTGGTCATTAAACC[C/T]GGTGGCCCAGCTTTT | 89910 |
rs569354479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109541587 | AGGTAACTCTCATTG[C/T]TGTTCTAAAACAATT | 89910 |
rs569376631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525385 | CTGTCTCGCAGGATC[A/G]TTCTCTACAGAATAG | 89910 |
rs569387212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109540941 | CCACGCAAGAAGTGC[A/G]GTGGGCGGGAGCTGA | 89910 |
rs569451187 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475992 | CAACCCCACTTTTTT[G/T]GGGAGAAAACTAGGA | 89910 |
rs569538291 | snp | A/G | 1.65195e-05 | 0.00287393 | intron-variant | UBE3B | GRCh38.p7 | 12:109524397 | TCTTAAGCACATAGT[A/G]CTCCATGGCCCTAAC | 89910 |
rs569651345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109481862 | GACTTAGTGTTTTTT[A/T]AAAAAAGTTGAAACC | 89910 |
rs569652799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528685 | ATGGTGAAACTCCGT[C/G]TCTACTAAAAATACA | 89910 |
rs569658152 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109516547 | CACTCTTTCCGGAAC[A/G]TTTTTTGCTTGTGTA | 89910 |
rs569679830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109481037 | ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 89910 |
rs569694852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523844 | GGAGATACTGCCCTC[C/T]GGATTGGAAACTTAG | 89910 |
rs569698539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109529330 | CATTGTAAGTTGCTC[C/T]GACTTCCCAGTTGAG | 89910 |
rs569750862 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109515588 | TGGTCAGGCTGGTCT[C/T]GAACTCCCGACCTCA | 89910 |
rs569825525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509767 | TGCACCCAGGGAGGC[C/T]GAAGAGTCTATGGCA | 89910 |
rs569826286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109522362 | AGCCAAGGTGGGACC[A/G]CCTTCAGTGGGAAGT | 89910 |
rs569832711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109503331 | AGCTGTTCCTCTTAG[A/G]GATTAGTCCACCTCA | 89910 |
rs569915425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109517151 | GAGCATCCACCTCTT[C/T]ATGTCCCTTTGAAAT | 89910 |
rs569956581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539870 | AGCAGCTCCTCCACC[C/T]GGGGACCAGCAGTTG | 89910 |
rs569989188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109508093 | GTGCAGATCCTTGCT[A/G]AGCAGATCTTGAGAC | 89910 |
rs569994424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539541 | TGCAGTTTCCTCTTC[C/G]ATGAAACGAGGATAG | 89910 |
rs570083324 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506502 | TACAGGTGCTGGCCA[A/C]CACGCCCGGCTGATT | 89910 |
rs570096018 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476703 | GCTCTCTCGATTTCT[C/T]TCCCTCACTGGGCCG | 89910 |
rs570155977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520691 | TGGGAAGGCAGCGGG[A/G]GATGAGGGGTGATGG | 89910 |
rs570193574 | snp | C/T | 0.000376293 | 0.0137115 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534095 | TAAAAACCCAGTGGC[C/T]GCCTCTGGGTGTAGC | 89910 |
rs570251728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109495318 | AAGAAACCTTTTTTT[C/T]CCCCTCTGTAAGTTG | 89910 |
rs570253731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487348 | ACTTTGCTTATAAGG[A/G]TAGAGAGGTCTCAGG | 89910 |
rs570266117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494597 | ATCAAGTAAGCAGTG[C/T]ACTTATAGACTTTGT | 89910 |
rs570345517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109518152 | ACTTCTGCGCCCTCC[C/T]GTTCTTGAAACAGCC | 89910 |
rs570459227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523899 | ACCCCTGGGCCATGT[A/C]TGCACCCTGAGCCAC | 89910 |
rs570461924 | in-del | -/GAAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528861 | TCTCAAAAAAAAAAA[-/GAAA]AGAAAAAGAAAAGGC | 89910 |
rs570582629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109508892 | ATGTGTCTTAGATAT[C/T]GAAAAGATTCTGCAG | 89910 |
rs570605529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482505 | GACTTTTTACTCTGG[A/G]TGATATTTTCATGTG | 89910 |
rs570622430 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109496755 | TTTTATGAGAGTTGT[A/G]AGTTCTTTATATGCT | 89910 |
rs570637635 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480617 | GATTGCACCACTGCA[C/T]TCCAGCTTGGATGAC | 89910 |
rs570667665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109504303 | ATCTTCAAATTTGGC[A/G]TTCAGCCAAATGCCC | 89910 |
rs570720547 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505741 | AATTGATACAATTCT[C/T]GGCCTCCTTTAGAAT | 89910 |
rs570752561 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535364 | CCTGCTAGGGACGCT[A/G]TGGACACCGTGAGTC | 89910 |
rs570756797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109529456 | GTTTTGACATGAAAC[A/T]ATTTTTTTCTATTTT | 89910 |
rs570808236 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478378 | TTTTGGATATACATG[A/G]ATTCAGATTCAAAAG | 89910 |
rs570821961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502293 | TGTGGGACTCCTTAT[A/G]AAGGAGCCACTCACT | 89910 |
rs570892677 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531167 | CACCCACAGTGTCCC[A/G]ATAAAACACACACAA | 89910 |
rs571103016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515648 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 89910 |
rs571138988 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109515217 | CGCGACTGGCCCATC[A/C]CCTTTCTTCTTAAGG | 89910 |
rs571155033 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109495413 | ATTCACATCTCATAC[A/G]CTTTATTCATTTAAA | 89910 |
rs571286827 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489141 | CCAGATGCCTCTAGG[C/T]GCTGAAGACAGATAA | 89910 |
rs571291011 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501987 | GTTCCACAACAATTT[G/T]GAGGCTTGTTAGGTC | 89910 |
rs571291643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109493310 | TGAGGCCTGAACTTT[C/G]AAGCTCAGGAGCAGC | 89910 |
rs571305686 | snp | A/G | 1.64912e-05 | 0.00287147 | intron-variant | UBE3B | GRCh38.p7 | 12:109533424 | CCGTCCTGGAAGAGC[A/G]GGAGCCTGCCCCGTC | 89910 |
rs571305885 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489738 | GCCTACCAGGAGAGA[A/G]AGAGTTCCAGGTACG | 89910 |
rs571342065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539070 | GTGAAACCCTGTCTC[C/T]ACTAAAAATACAAAA | 89910 |
rs571343858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533180 | GCCCTGGCTGGGCAT[G/T]TGTGCTGTTCCTACT | 89910 |
rs571369937 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484093 | AATTACTGTCACCCT[C/T]ACATCCTGTCCCTTT | 89910 |
rs571379435 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109538534 | GAGGATTAAATGCAG[A/T]TACATATGACGCACC | 89910 |
rs571380686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109537601 | TCATGTAACTAAAAG[A/C]AAAAACAGTGTAACC | 89910 |
rs571412671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532565 | AGAACATTCTTGGCT[A/G]CTGTTGAGTTAAAGT | 89910 |
rs571419691 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109522424 | CCAGGAGGAAGGAAA[A/G]CTGCAGCACAAGCCC | 89910 |
rs571447845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523095 | AGAAGATGGGACCTG[C/T]TAGGCCCTGCATGAG | 89910 |
rs571468308 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519570 | CGTGTGAAGGCTGGG[A/G]AGGCATAATTTTAAA | 89910 |
rs571605594 | snp | A/G | 9.91654e-05 | 0.0070408 | intron-variant | UBE3B | GRCh38.p7 | 12:109521363 | GGCTGACAGCAGCCA[A/G]ATTCAAGAAGTGAAG | 89910 |
rs571617468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526669 | CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGATCA | 89910 |
rs571746444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499555 | GATGTGGCCGCCTGA[A/G]CCACAGGCAGGGAGC | 89910 |
rs571758349 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477444 | TAGGGGCCAGTTTTC[C/T]TTCCAGCCTCCCCGG | 89910 |
rs571816648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485604 | GATGATACAGCAGCC[C/T]TTGGCTACTGGCTGT | 89910 |
rs571888292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109501693 | GTCTCACTGTATTGC[C/T]CAGGCTACAGTGCAG | 89910 |
rs571993667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109514914 | CATCCCCTTTCTTCT[C/T]CTTTTTTTTTTTTTA | 89910 |
rs572010570 | in-del | -/TTTTTTGT | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490803 | AAACACTGCATACGG[-/TTTTTTGT]TTTTTTGTTTTTTTG | 89910 |
rs572079698 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109544123 | TCTGGCCCCAGCAAT[A/C]ACAACAAAACAACCT | 89910 |
rs572099258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109539317 | ACCCTCTGGAGCGTG[C/G]GGTCAGAATGGCATC | 89910 |
rs572118676 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109522482 | GCTCCAGAGCTGCAG[C/G]GACCCTGCCTGGGTC | 89910 |
rs572155552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109521769 | TGTGACGGGGCTGCC[A/G]CTGTCCTGGCTATTT | 89910 |
rs572159682 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511040 | GTAGCACAAAAGCTG[-/C]CCATAGGCTATACAT | 89910 |
rs572196146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109527501 | TGCACGTCGCAGTCC[A/G]GTGTTCCCAAGCATC | 89910 |
rs572198132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513182 | GTGTCTGGTTTAAAA[C/T]GCAGCCCCTCCTCCT | 89910 |
rs572270375 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109537027 | AATATTCTTTTTTTG[C/T]TTTTTTGAGATGGGG | 89910 |
rs572294299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478540 | AATCCTAGCACTTTG[G/T]GAGGCCGAGGCGGGC | 89910 |
rs572314190 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493209 | AGATTCACTGCAACT[C/G]TCCCTACCCAAGTCA | 89910 |
rs572314590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515319 | ATATACTAGCACCCA[A/C]TGGTATATAGTATTT | 89910 |
rs572321343 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506825 | CTAGAAGTCTAACTT[A/C]GGACTATTCAGTATT | 89910 |
rs572393077 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531932 | ACCAAACCTACAGTT[A/C]CTTACCATGTGCCTG | 89910 |
rs572433144 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534178 | CACAGTCCTCGGCCT[C/G]CATGCTTAAGGGAAA | 89910 |
rs572433471 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503629 | CCAATAATCATTTTA[C/T]CATGTCACAAATTCT | 89910 |
rs572449769 | snp | C/T | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109499180 | TGACTAACTGGTGAA[C/T]GTTGAATAACAGCGA | 89910 |
rs572453418 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479303 | CATGCTTTTAGATAT[C/T]CTATATTAATATTTT | 89910 |
rs572456973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109512816 | AGTGAAGGGCCTTAC[A/G]GCAATTACTTAATCA | 89910 |
rs572468447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531443 | CACCAGCCTTCCTAC[C/T]TGACAGAATATCAAT | 89910 |
rs572473883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109513757 | CCTTAGTTCATAAAA[A/T]GTCCTCCCTCAGGAA | 89910 |
rs572557235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109485879 | ATCTGTAGGAAGGAA[C/G]TGCATGTGATTATGT | 89910 |
rs572564875 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476906 | ATGTCCGTTTTCAAT[A/T]GATATCTCTTTGTTC | 89910 |
rs572591928 | snp | A/G | 8.31331e-05 | 0.00644668 | intron-variant | UBE3B | GRCh38.p7 | 12:109486448 | ATAACAGCCCATGAC[A/G]TTCCTCTTTTTCCCA | 89910 |
rs572604514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109493368 | ACAAGCTCTAGGAGC[A/G]CCTCACCTTTCTTAC | 89910 |
rs572620204 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109492461 | AAAAAGCCAAAAGAG[G/T]CCAGGCACGGCGGCC | 89910 |
rs572683549 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109538263 | TGGGTTCTCGCCAAG[C/G]TTGGCGAGTAAATCC | 89910 |
rs572694451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538677 | AAGCTTCCAGAGTGG[C/T]TCCTGCTGCTGCTGA | 89910 |
rs572755168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490826 | TTTTTTGTTTTTTTG[G/T]TTTTTTTTTAAGAGA | 89910 |
rs572774756 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | UBE3B | GRCh38.p7 | 12:109532828 | TCATTTTTGTCAGTG[G/T]GCTGAGAGGTTATTA | 89910 |
rs572783543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526157 | AGGATTGGGTGAGAA[A/C]AAAACCTTTTGTATT | 89910 |
rs572819144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109497745 | TAGGAATTTGAGCAC[A/G]TTGGTGGGGTTGTGC | 89910 |
rs572824539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525787 | AGCAAAAGATGAAAA[A/G]ATAATGAAACTTCTA | 89910 |
rs572838524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109523689 | GTGCTGCCCCCCACT[C/G]ACAGGTGAGACAGCT | 89910 |
rs572845808 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536499 | TTTTGACAAGGAGGG[A/G]TAGTTTGTAATTTCA | 89910 |
rs572863270 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476044 | TGACTCCCAACTCCT[A/T]TGCCCCTTTCATTAC | 89910 |
rs572905203 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528481 | AAGCTTTAGCATTGT[A/G]AAACATTTATTTGGA | 89910 |
rs573036001 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3B | GRCh38.p7 | 12:109482697 | CCGGGGGTCAGTGCT[A/G]TGTGCTTTAGGCTGC | 89910 |
rs573082806 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109505198 | CTATTTAGCAACTTA[A/G/T]ATTATAGAAAATAAC | 89910 |
rs573096712 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477662 | CAAGATGGCGGTAGT[C/G]CGTCGGCTGCTGCCC | 89910 |
rs573114657 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526849 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 89910 |
rs573144345 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536253 | ATTGAAGGTGTGTTC[A/G]TAACCTCTGATTCTG | 89910 |
rs573156019 | snp | C/T | 1.65181e-05 | 0.00287381 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511269 | GGGCACAGTTGATCC[C/T]GCAGTACATCCCACA | 89910 |
rs573201906 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477148 | AATGCCTCTCCACTA[G/T]CGTGACTGCCCCTCA | 89910 |
rs573218566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109510516 | CTCCGGCACGCTGCC[C/G]GAGCACTCAGCTCTC | 89910 |
rs573354818 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109542106 | TTCTTCATGCCATGA[A/G]CCACCACATGCTCAC | 89910 |
rs573364796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497240 | TTATCTGTCCTCAAT[A/C]TTTTAAAAATGTATC | 89910 |
rs573366585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109491734 | GGGAGATGTTAATAA[A/G]AGATCCTGGAAGGAA | 89910 |
rs573421352 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532057 | AATGTAAAGCAAGCA[A/G]AGCATCCAGGGGTTT | 89910 |
rs573465629 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109518549 | ACTTCCCTCTGCAGA[C/T]CCAGATGCATCTCCC | 89910 |
rs573503568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109504788 | TGAGAGGAGTTTGGG[A/G]TTGTGGTTTGTGTCC | 89910 |
rs573548033 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477707 | CTCGGGTGTTTTGGG[C/T]TGAGACAGTGGCAGC | 89910 |
rs573561397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520818 | AGAGAGAGAGAAATG[C/T]ATCTTGTCCCGGTTT | 89910 |
rs573570449 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3B | GRCh38.p7 | 12:109485757 | GAAGCCTCAATTTGG[A/G]TTTTTATGTGAAGTA | 89910 |
rs573589439 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541335 | GCCTTGACCTTGGAC[C/T]TGTACTTGAGCTCGG | 89910 |
rs573599332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109520291 | CAGCACCCCAAGTAC[C/T]AGGAATGCATTAGAT | 89910 |
rs573791586 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539196 | AGCCAAGATCACACC[A/G]CTGCACTCCAGCTTG | 89910 |
rs573796970 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109487457 | AATCCATTCCCAGCC[A/G]TCCCTCTTTGGCTGC | 89910 |
rs573849357 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532534 | GTGACAAGCCCCTGT[A/G]TCCCCTAGAGAAGGG | 89910 |
rs573881235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109526862 | GGCGACAGAGTGAGA[C/G]TCCGTCTCAAAAAAA | 89910 |
rs573907809 | snp | C/T | 0.000179905 | 0.00948261 | intron-variant | UBE3B | GRCh38.p7 | 12:109517877 | TCTTCATTTTCTCCC[C/T]CGGTGCATCGTACCT | 89910 |
rs574111725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109496373 | TTTTGTATAGACATA[C/T]GTTTTCATTTCTCTT | 89910 |
rs574146073 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3B | GRCh38.p7 | 12:109518686 | AGAGTGGCAGAATCC[A/G]ACTCCCTTCACAAAT | 89910 |
rs574182680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525112 | CTTATTAGACTCGCG[C/T]TTGGGCACCTCAGAA | 89910 |
rs574228868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109481816 | ACCGTTTCTCTCCAA[A/G]CCTTTTATAAGTTGG | 89910 |
rs574264585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109511769 | TTTCTGCAAAGCCAC[C/T]GGAGGGCTGGAAGCT | 89910 |
rs574285673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475555 | AATCAGTATCTCAGA[C/G]ATGCGGAGGGGTGGC | 89910 |
rs574380585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109542760 | AGGAACAGATTCTCC[C/T]TCACAGCCTGGAGAG | 89910 |
rs574453691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109528885 | AAGAAAAGGCCAGGC[A/G]TGGTGGCTCACATCT | 89910 |
rs574489513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510018 | TTGATTTCCGTGAAG[A/G]TAAAACATGTGCCAG | 89910 |
rs574525798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109495720 | AACAAAGGGATGGGC[C/T]GAAATAAAGGGATGG | 89910 |
rs574536035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109502825 | GGGTATTCTGAAGAG[A/C]TCTTTGGGTTGTACC | 89910 |
rs574539443 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483572 | CACCCTGTCTCAGAC[C/G]TCGAGAGCATGGTTC | 89910 |
rs574586129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109530794 | ATCCTCTCCCACAGG[C/T]AGGCCTCCCGGTAGG | 89910 |
rs574639065 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBE3B | GRCh38.p7 | 12:109489506 | TTATTTCAGGCATGA[A/C]CCTGGCCTCTTGGGG | 89910 |
rs574653873 | snp | A/C | 0 | 0 | intron-variant | UBE3B | GRCh38.p7 | 12:109530349 | TGGGAACAGCAGGGC[A/C]AGCTCTCAAATTCCC | 89910 |
rs574690634 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535598 | AGCCTGCTTGTCCCG[C/T]GGAGGACGGCTGCCT | 89910 |
rs574723857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524798 | ATGGTGAGGATTAGC[C/T]GTTACAAATGGAGGA | 89910 |
rs574782044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487671 | TTCCACAACAGATTG[C/T]TCTTTGAGGAGAAGC | 89910 |
rs574802003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487088 | TGTAATCATGGCAAC[A/G]AGCAGTTTTGACTTT | 89910 |
rs574814881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109529572 | GTACTAAGAAGGGCC[C/T]TCTTCTTACGTGGGG | 89910 |
rs574851448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533790 | CTTTCTCTTTCCTTC[C/T]TCAGGGAAGGGTACC | 89910 |
rs574858098 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478472 | AAGTCGTGTTTCCTA[C/T]TCTTTAAATAAAAAT | 89910 |
rs574971788 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523351 | CAGCTCTGTCCCTTC[A/C]CTGCTCAGAGCCCTC | 89910 |
rs575013906 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526644 | TTGTTAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 89910 |
rs575020345 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109516340 | CCACACCCAGCTAAT[G/T]TTTGTATTTTGTATT | 89910 |
rs575025353 | snp | C/T | 3.29652e-05 | 0.00405974 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516785 | TCTACTGTTTCGAAC[C/T]ATGGTTACCAAGGAG | 89910 |
rs575057328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109482018 | TGATATGTTCATGTG[G/T]TGGGAGGCTTGCACC | 89910 |
rs575144023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109497187 | TAAAAAAGAAAAAAA[A/T]TTCTCATAATTCTAC | 89910 |
rs575222164 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109504624 | GCTGGCAGAGGTGAC[A/T]CTCTGGGAGCATCAG | 89910 |
rs575304347 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477094 | TCTCCACCCAAAGCC[A/C]TTCCCCCACCCCGGG | 89910 |
rs575309508 | snp | A/G | 3.36905e-05 | 0.00410416 | intron-variant | UBE3B | GRCh38.p7 | 12:109490049 | CTTCTCCACTCTCCA[A/G]CACCTGCACTTGGAT | 89910 |
rs575369954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109488318 | TGGTCATCTTGTTTT[C/G]TAGGGATTCTCAATT | 89910 |
rs575393015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109525728 | TTTTCTCCCGACTAT[A/G]AAGATAATGAAACTT | 89910 |
rs575415880 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476286 | ATTTTGCACAAAATG[A/G]AGCGGACTAGTCAAC | 89910 |
rs575418595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109511148 | ATTTCCCAGCCTCAC[A/G]CTAGAGGATGGTTTC | 89910 |
rs575427913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109531277 | AAAGTTGTAAATGTT[C/G]AAAATATTCCCCTAA | 89910 |
rs575459519 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109528963 | CAGGAGTTTGAGACC[A/G]GACTGGTCCAACATG | 89910 |
rs575475140 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109525220 | CGCTGGGAGCCCTGC[A/G]TGGCCTGTCCTCCTG | 89910 |
rs575480347 | snp | C/T | 0.000235392 | 0.0108462 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510438 | GCGGCGCTTCACCCC[C/T]GAGGACCACTGGCTG | 89910 |
rs575535776 | snp | C/T | 1.65471e-05 | 0.00287633 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516866 | TCACATCACCATCCG[C/T]CGGTCCAGGATGCTG | 89910 |
rs575564775 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109521024 | CTCCTGTCATGCATC[A/C]ACGTTTCATAATTTG | 89910 |
rs575646965 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490615 | CCTTCTACTTCATAC[A/C]ATAATTAAACGGCTT | 89910 |
rs575829703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487704 | TTCTATTTTGGACAA[A/G]CAAAAAAAGTTTATG | 89910 |
rs575852949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109524667 | TCTTGCCAGGAGGGA[A/G]GGCCCCCTCCTTTCC | 89910 |
rs575931932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109501131 | TTCGAGAAGAGTGTG[A/G]CTCATGGAGCTTGGG | 89910 |
rs576003067 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109508428 | GCAGTGCCTGGCACA[C/G]AGTGGGAAATTAACA | 89910 |
rs576085837 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507872 | CATTGTAAGAACTAG[C/T]CATTTACCAAGTGAG | 89910 |
rs576116612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538324 | TGGAAACTTATCAAA[C/T]TGGCCAGAGTGGCCG | 89910 |
rs576134003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109515970 | GGTCAGGGAGCTTTA[C/T]ACTGTAGGGTCATTT | 89910 |
rs576191716 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | UBE3B | GRCh38.p7 | 12:109492403 | GGACAAGGCTGACCT[-/AG]AGAGCAGGTCTGTCC | 89910 |
rs576196991 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535348 | CAGGGAAGCGCAGGC[A/G]CCTGCTAGGGACGCT | 89910 |
rs576235087 | snp | G/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536813 | GGAAGATGTGGAGGG[G/T]CGCAGAGCACATGTC | 89910 |
rs576261249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109501789 | CAAGTATAATAGCTG[A/G]GACTACAGGCGTGTA | 89910 |
rs576502683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109493454 | AACATGCTCACATCC[A/G]GTCATTCTACCACAC | 89910 |
rs576516150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109492572 | ACATGGCCAAACCTT[G/T]TCTCTACAAAAAATA | 89910 |
rs576643870 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476513 | ACAGCTGAGAGACAG[A/T]TCTTGAAACATCCTC | 89910 |
rs576677571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109533267 | ATGTGTCTTAGTCCC[C/T]GAGAGCAGCACCCTT | 89910 |
rs576713034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109486922 | CACAGCTAGTATCAC[A/G]TACCAGTTAAGCAAG | 89910 |
rs576774365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109494059 | TCAAACTCCTGGCCT[C/T]AAGCGATCCTCATGC | 89910 |
rs576782910 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534946 | AGAAATTTAGACGCC[C/T]ACGACAGCACTACAC | 89910 |
rs576865126 | in-del | -/T | 0.216649 | 0.247765 | intron-variant | UBE3B | GRCh38.p7 | 12:109504972 | ACCATGCCCGGCTAA[-/T]TTTTTTTTTTGTATT | 89910 |
rs576878536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109516174 | TTTTTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 89910 |
rs576956735 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109501837 | TTTTTTTTTTTTTTT[A/T]ATTTTTGTAGAGATG | 89910 |
rs576958566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509866 | AATTTTCTTTCTTCA[C/G]TCTCTGTGACTTCTT | 89910 |
rs576959895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109538863 | GGATCCAGCCAAGGC[A/G]TTTCCAGGCCCCTGT | 89910 |
rs576968479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109509168 | GTACCACCTCACAGC[A/C]AGTTTTGCTTCATCC | 89910 |
rs576973581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109496169 | GGAATCACATCATAT[A/G]TGGTCTTTTGCTACT | 89910 |
rs576977166 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109488406 | CATTCCCTGTTATTT[A/C]ACTCCTGGAGTGGTC | 89910 |
rs577061967 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109541144 | CACCTGCCTGCGGCT[C/G]AGTGGCCTTCAGCTA | 89910 |
rs577069407 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535535 | GGGAAGAAAAACAAC[A/G]GCCCTTAGCAGCAGC | 89910 |
rs577105418 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109540388 | AGTTTATTTTGTATT[A/T]TTTATAGAAACAGGG | 89910 |
rs577175530 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479010 | ACAAGAGTCTGAATC[C/G]TGCCTCTTAGTTATT | 89910 |
rs577203772 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109535119 | CGTCTGAGTGAGCTG[C/T]GTATGAACAAGTCCC | 89910 |
rs577239113 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3B | GRCh38.p7 | 12:109493632 | TATAATTGAACACAA[C/T]CAGGACCTTTTAAAG | 89910 |
rs577240291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109500847 | GTACTCAGGGGTGGC[A/G]GCTATTAACAATATG | 89910 |
rs577306098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109487006 | GAGAGCTAGGGGGTT[C/G]TGATTCTCCCTCTCA | 89910 |
rs577398805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109508127 | CTGGGCAAGGGATCA[C/T]GGATTCAACCTCTCT | 89910 |
rs577415282 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496400 | CTTGGGCATATTCCT[-/G]GGGAGTAGACTTCCC | 89910 |
rs577449109 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3B | GRCh38.p7 | 12:109522659 | GGGCCAAACTCCTTT[C/T]ACTCTCGAATAATCC | 89910 |
rs577482321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109514851 | TCTAGATCTGTCAAC[C/T]AGCCTCAGCAAGATG | 89910 |
rs577521597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109514029 | TGTTGAACCTCTCCC[C/T]TGTTCTCGATTTCAC | 89910 |
rs577522609 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526893 | AAAAAAAATTGATTT[A/G]CAAAATAAGAATTGA | 89910 |
rs577744805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499879 | TCTTCCTTCTTTCTT[C/T]CTTCCAGCTTGTGGT | 89910 |
rs577770802 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541105 | ACCACTGCTGCATCC[C/T]TCAGACCATGTTCCA | 89910 |
rs577777455 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514502 | TCTTTAGTTCTGTTT[C/G]TGTGTCTTCTGCTAT | 89910 |
rs577806733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109484637 | CCTTGTGATCTGCCC[A/G]CCTCAGCCTCCCAGA | 89910 |
rs577815659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109492377 | ACTTCCAGCATCACA[C/G]AAAGTTCTGTTGGAC | 89910 |
rs577823861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109491808 | CCCCCATCTGTGGAT[A/C]TACAGTACACCTTCA | 89910 |
rs577914586 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507103 | TTTAACAGCAGAGAC[C/T]TTCTGGCCCACAGTG | 89910 |
rs577953919 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | UBE3B | GRCh38.p7 | 12:109479614 | TAATAAACACTTGAT[-/TG]TGTGTTTTATTAATT | 89910 |
rs578005002 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBE3B | GRCh38.p7 | 12:109505318 | GCTGCTGGTCTGTCT[G/T]CCATTGCTCTGCCAG | 89910 |
rs578120021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109511785 | GGAGGGCTGGAAGCT[C/T]AGGAGGCACCTGGTC | 89910 |
rs578130191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109499144 | AGGAGTTTCTGGTGC[A/G]AATGTTCACACGAGT | 89910 |
rs578147674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3B | GRCh38.p7 | 12:109519251 | CCAGGCATCCCTTTT[C/T]TAGCTCAGTATTCCC | 89910 |
rs578166494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109498456 | TGTTTTCTGTAACAA[C/T]TGGAAGTGCTTACAA | 89910 |
rs578187097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3B | GRCh38.p7 | 12:109532289 | ATTCAGGGAATGCTC[A/G]TCACAGTGTGGAAAC | 89910 |
rs578195204 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109544047 | GCCTCAGACTGCAGG[G/T]TGTGTTTGGGAAGCA | 89910 |
rs672601304 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483552 | TGCAAGTTTGCAAAC[A/G]TGTTCACCCTGTCTC | 89910 |
rs672601305 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510375 | GACCTTGGAGCTGTT[-/C]CAGTCTGTCCACGGG | 89910 |
rs745305989 | snp | C/T | 1.7573e-05 | 0.00296415 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499661 | CTTGGGCTCCCTCAG[C/T]CCCAGAGTGTTAGAG | 89910 |
rs745306464 | snp | C/T | 7.18856e-05 | 0.0059948 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510348 | TTGTCCCACAGAGAA[C/T]GCCAAGGGTGAGACC | 89910 |
rs745325113 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507468 | ATTAAATGTTCATGG[A/T]TAGGTTTAAGTGTTT | 89910 |
rs745426222 | snp | A/G | 3.38593e-05 | 0.00411443 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534622 | TGGGCAGCGTCCTCC[A/G]GGGCTTCTTCACCAT | 89910 |
rs745446082 | snp | A/G | | | missense | UBE3B | GRCh38.p7 | 12:109543546 | AGCCACACTTTAAGA[A/G]GGATGCAGGAGGCTG | 89910 |
rs745469763 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476225 | GGTGGGACCAGAGTT[-/TG]AGAACCACTGGTTTA | 89910 |
rs745492079 | snp | A/T | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109526384 | TGAACTGATTCCTGG[A/T]GGGAAGACCATTCCT | 89910 |
rs745509722 | snp | C/T | 9.88614e-05 | 0.00703 | intron-variant | UBE3B | GRCh38.p7 | 12:109489907 | TTTGTTCTCACTGTT[C/T]TCTTTCTTTAGGTGA | 89910 |
rs745516932 | snp | A/G | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499744 | GGAAGTATGTGTCTC[A/G]GAAGAAGTCCAACCT | 89910 |
rs745518534 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109529906 | ATTAGCTACATCCAT[C/T]TGATGGCACATTTTC | 89910 |
rs745562218 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483501 | TTCACACAACAATCT[A/G]CAACACCCACTTGCC | 89910 |
rs745564831 | snp | C/T | 1.64972e-05 | 0.00287199 | intron-variant | UBE3B | GRCh38.p7 | 12:109490020 | GTCTGTGACTCCTGC[C/T]CCCCAGTGTGCAACT | 89910 |
rs745569236 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481135 | AATGTCAAACATGGC[C/T]GGGCACAGTGGCTCA | 89910 |
rs745611524 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484503 | TTCAAGCAGTTCTCC[A/G]GCCTCAGCCTCCCTA | 89910 |
rs745711632 | snp | A/G | 0.000131774 | 0.00811601 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521218 | GTGTGAAGTTTGTCA[A/G]TGACCTCGGGGTGGA | 89910 |
rs745713775 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530630 | TGGCCTCCGACTTCA[C/T]ACCGGATGAGAGAGC | 89910 |
rs745747381 | in-del | -/TTAA | 1.65474e-05 | 0.00287636 | intron-variant | UBE3B | GRCh38.p7 | 12:109529853 | GCCTGCCCCGTCCTG[-/TTAA]TTGTCATTGTTATCT | 89910 |
rs745755711 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109499123 | TCCCTGGGGCCAAAT[G/T]TCATGAGGAGTTTCT | 89910 |
rs745759304 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486320 | TGCGTTTAGTGTTAA[-/T]AATAAGTCCTGTTTA | 89910 |
rs745768897 | snp | A/G | 1.65438e-05 | 0.00287605 | intron-variant | UBE3B | GRCh38.p7 | 12:109521368 | ACAGCAGCCAGATTC[A/G]AGAAGTGAAGAGCTG | 89910 |
rs745803105 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501059 | AGCCAGCTATGAGGA[A/G]GGAGGCAGTGCAGTG | 89910 |
rs745812554 | snp | C/G | 1.65146e-05 | 0.0028735 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509667 | TGGTCACTATCTCCT[C/G]TTTCCTGAATTCTTT | 89910 |
rs745815924 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532934 | GCACCTGTGCAGTCC[C/T]CTCTGCATGAATAAG | 89910 |
rs745839378 | snp | C/T | 8.12579e-05 | 0.00637357 | intron-variant | UBE3B | GRCh38.p7 | 12:109486098 | GGAGCCGCAGTGTCT[C/T]CCACAAGCTCTTAAG | 89910 |
rs745858129 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489443 | GAGCGGGGATGAAAC[A/G]GAAAGCAGGGAAAGC | 89910 |
rs745881276 | snp | C/T | 1.65326e-05 | 0.00287507 | intron-variant | UBE3B | GRCh38.p7 | 12:109498216 | TTTCTGATTTAACGG[C/T]CTGCTATTCTTTGCA | 89910 |
rs745905368 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486535 | TTCAACAGATCAAGA[A/G]CATTTTGTGGTACTG | 89910 |
rs745937313 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493744 | AATCCTGAAATATGA[A/G]TAGCTAACATTCATG | 89910 |
rs746003315 | snp | C/T | 1.65425e-05 | 0.00287593 | intron-variant | UBE3B | GRCh38.p7 | 12:109523961 | TGATGGACAGCTCTG[C/T]TTCTCTGCTCTCCCA | 89910 |
rs746006243 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109521963 | AGGCTGGGTCCCCGT[C/T]GTAGGAGGGCAGCAT | 89910 |
rs746041287 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519397 | TATCACAAGAGGCAG[C/T]CCCCTCTAAACGTTT | 89910 |
rs746051489 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109509300 | AGGATACATGTGCTG[A/G]AAGTGCAGGTTTGTT | 89910 |
rs746058354 | snp | C/T | 4.82905e-05 | 0.00491355 | stop-gained, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510454 | GAGGACCACTGGCTG[C/T]GAAAGTGAGCTCCAG | 89910 |
rs746077832 | snp | A/G | 2.06969e-05 | 0.00321683 | intron-variant | UBE3B | GRCh38.p7 | 12:109486614 | AAAAAGCAAAACCAG[A/G]AACAGTACGTATGTC | 89910 |
rs746084692 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523387 | AGAATCCAGCCTGCA[A/G]CAAGGCTTACGGGCC | 89910 |
rs746100402 | snp | C/T | 1.65179e-05 | 0.00287379 | intron-variant | UBE3B | GRCh38.p7 | 12:109501342 | ATCAGATGGAACTGA[C/T]AGACCAGGTCTCCTC | 89910 |
rs746106778 | snp | C/T | 1.82533e-05 | 0.00302098 | intron-variant | UBE3B | GRCh38.p7 | 12:109511184 | TTTAATTCTCCCAAA[C/T]CCATGTCTTTCTTCT | 89910 |
rs746130124 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510116 | TTAAAAGGCCCTTCG[A/G]ATGACACACTAGTGG | 89910 |
rs746154533 | snp | C/T | | | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516863 | CACTCACATCACCAT[C/T]CGCCGGTCCAGGATG | 89910 |
rs746229005 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535417 | AGCCACGCGCTCCAC[A/G]CCGCGGCCCTCCCAT | 89910 |
rs746232379 | in-del | -/GC | 1.72597e-05 | 0.00293761 | intron-variant | UBE3B | GRCh38.p7 | 12:109501585 | CTTGGCTGAAGTACA[-/GC]GCTCCTGTTTCTTCC | 89910 |
rs746238845 | in-del | -/CCTAGAC | | | intron-variant | UBE3B | GRCh38.p7 | 12:109509228 | TATTTTGAAGCAAAT[-/CCTAGAC]ATCATATCATTTTTT | 89910 |
rs746301277 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503091 | CCTGTCGGGGGTAAA[C/T]GGGTCGACTCTGCAG | 89910 |
rs746325229 | snp | A/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533469 | TTTGTGTTGCAGTTC[A/G]TGACCAGCTGCTCCA | 89910 |
rs746333199 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528956 | CCGAGGTCAGGAGTT[C/T]GAGACCAGACTGGTC | 89910 |
rs746352099 | snp | A/G | 1.64985e-05 | 0.0028721 | intron-variant | UBE3B | GRCh38.p7 | 12:109503205 | GGTTCGCAGTCCCCA[A/G]GGCATCTTCTTCACC | 89910 |
rs746369635 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485637 | GGCAAAAGTCAGTAT[C/T]CATGGTGCTTAAGAA | 89910 |
rs746387554 | snp | A/G | 1.65616e-05 | 0.00287759 | splice-donor-variant | UBE3B | GRCh38.p7 | 12:109533559 | GTGTCGGACGATCAG[A/G]TACCCCCACGGGGTG | 89910 |
rs746405663 | snp | A/T | 1.64806e-05 | 0.00287054 | intron-variant | UBE3B | GRCh38.p7 | 12:109497940 | TAAGCAGGCTCTGTG[A/T]GTTCCCCGTGAAAAC | 89910 |
rs746462871 | snp | A/C/T | 8.26038e-05 | 0.00642622 | intron-variant | UBE3B | GRCh38.p7 | 12:109501329 | GCCCTGGCCCTGCAT[A/C/T]AGATGGAACTGACAG | 89910 |
rs746483758 | snp | C/G | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475440 | CAAGATAATACCAGT[C/G]CACTCTCCAGCCTGG | 89910 |
rs746526539 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541703 | CTCGGACAGTTCTGG[C/G]CAGAAGCCTGAAATC | 89910 |
rs746578379 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109529930 | CATTTTCGAATGCAC[A/G]CTCAAATAAAAAACC | 89910 |
rs746624505 | in-del | -/AGCAGCATGGAT | 1.77212e-05 | 0.00297663 | cds-indel, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486042 | TGTCGCAGCATCCTG[-/AGCAGCATGGAT]GCTGAGAATGAGCCT | 89910 |
rs746631323 | snp | A/G | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516844 | GCTCTGCCTCCCCGC[A/G]TGTCACTCACATCAC | 89910 |
rs746633637 | snp | C/T | 4.94173e-05 | 0.00497053 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530014 | CGAATGTTCTCAACT[C/T]CTGAACTGCAGCGTC | 89910 |
rs746633699 | snp | A/G | 1.6734e-05 | 0.00289253 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483601 | TCATCGATAGAGCCC[A/G]TCAGGCACGAGAAGA | 89910 |
rs746667475 | snp | C/T | 2.5702e-05 | 0.00358474 | intron-variant | UBE3B | GRCh38.p7 | 12:109490095 | CAGCATACCTGGTGT[C/T]CTCCTCAGAAACACT | 89910 |
rs746676812 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494104 | AAGTGCTGGAATTAT[A/G]GGAGTGAGCCACCAC | 89910 |
rs746682731 | in-del | -/TTT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484924 | ACCATGCACAGCAAG[-/TTT]TTGTATTTTTTGTAG | 89910 |
rs746682760 | in-del | -/G | 1.93489e-05 | 0.00311032 | intron-variant | UBE3B | GRCh38.p7 | 12:109486603 | AAAAAAAAAAAAAAA[-/G]GCAAAACCAGAAACA | 89910 |
rs746688590 | snp | A/G | 1.68119e-05 | 0.00289926 | intron-variant | UBE3B | GRCh38.p7 | 12:109516930 | AAGGAAGTGGGCCCT[A/G]CAACATGGAAGCTCT | 89910 |
rs746694145 | snp | C/G | 1.65081e-05 | 0.00287293 | intron-variant | UBE3B | GRCh38.p7 | 12:109503214 | TCCCCAGGGCATCTT[C/G]TTCACCTCTCACATT | 89910 |
rs746722966 | snp | C/T | 1.69479e-05 | 0.00291095 | stop-gained, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483693 | TTTCTCTGTCGGAGT[C/T]GACTGCAGAGAGATA | 89910 |
rs746732023 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482569 | GATTGTTTTCTGGAA[A/G]TCTGGATTTCTGAAT | 89910 |
rs746811263 | snp | A/G | 4.94539e-05 | 0.00497238 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486493 | ATGTGTCCCTGGCTT[A/G]TTCTAAGGACCTCAC | 89910 |
rs746890451 | snp | C/T | 1.71669e-05 | 0.00292971 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521512 | TTACCTGCAGCTCTT[C/T]GAGTTTGTGGGGAAG | 89910 |
rs746925407 | snp | C/T | 1.6867e-05 | 0.002904 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534639 | GGCTTCTTCACCATC[C/T]GCAAGCGGGAGCCAG | 89910 |
rs746934413 | snp | C/G | 3.44893e-05 | 0.00415252 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534725 | CAGCAAGAAGAGCGT[C/G]CTCCGCGAGAAGCTG | 89910 |
rs746952158 | snp | G/T | 1.64904e-05 | 0.00287139 | intron-variant | UBE3B | GRCh38.p7 | 12:109526436 | GTATAGCAATTAGGT[G/T]TTTAAGGTCACCACT | 89910 |
rs746954929 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514014 | ACCATCTGCCCTAAA[A/T]GTTGAACCTCTCCCT | 89910 |
rs746977582 | snp | C/T | 4.95749e-05 | 0.00497845 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499762 | AGAAGTCCAACCTGA[C/T]CCACTGGCATCCTGT | 89910 |
rs746999758 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501005 | GGAAACACTGAGGAG[A/G]CTGCTGAGTCATCTA | 89910 |
rs747012515 | in-del | -/TC | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533651 | CTTATCTAGTCCATA[-/TC]TCAGCAAGGCAGGCA | 89910 |
rs747030779 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488459 | AAGACTGACTTATAA[G/T]CCTGACTCAGTGATT | 89910 |
rs747033125 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488616 | CACCCTGTACCTCAC[A/G]ATGCTTGTCACCTTC | 89910 |
rs747112092 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531785 | CCCAGAAGTGCCTCA[C/T]GGGCAAAGCAGTTTC | 89910 |
rs747158016 | snp | A/G | 1.66888e-05 | 0.00288862 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511212 | TCTCAAGGGATCTCA[A/G]ACCTAGCGTGCTCTT | 89910 |
rs747165379 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520620 | CCTTCTGCAGCTCCC[A/G]TTACCTTCAGGATGT | 89910 |
rs747175384 | snp | A/C | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511277 | TTGATCCTGCAGTAC[A/C]TCCCACATGTCATCC | 89910 |
rs747207308 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501425 | GTTCTTGTGGGGGGT[A/G]CCTCTGATCCGGATC | 89910 |
rs747227099 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489347 | GGTGGGGAGGCCTTG[C/T]TTGGTCTGGGTCTCT | 89910 |
rs747230707 | snp | A/G | 8.24069e-05 | 0.00641846 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491076 | GCCTGGCAAGACCCC[A/G]TCCTTGTCTATCCAA | 89910 |
rs747235597 | snp | C/G | 1.6543e-05 | 0.00287597 | intron-variant | UBE3B | GRCh38.p7 | 12:109530504 | CCTGTCCATAAGTGC[C/G]CACGCTAGCACATTG | 89910 |
rs747273441 | snp | C/T | 1.67643e-05 | 0.00289515 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507568 | GTTTTTTCCAGGTCT[C/T]ACTTACCTTGATGAC | 89910 |
rs747311414 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508973 | ATGAATAAGGAAGGC[A/G]TGAATTGAGGTGTGA | 89910 |
rs747337543 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479939 | TTGAGGCACTGTCTG[C/T]ATGTCATGGAGGGAG | 89910 |
rs747380038 | snp | A/G | 3.31702e-05 | 0.00407235 | intron-variant | UBE3B | GRCh38.p7 | 12:109533569 | ATCAGGTACCCCCAC[A/G]GGGTGGGTGGGGAAG | 89910 |
rs747423628 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537848 | TAGCTGGGACTACAG[A/G]TGCCCGCCACCTTGC | 89910 |
rs747429223 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538775 | GGAAAGTCACATTCC[C/G]TCATCCACACTGCCG | 89910 |
rs747433142 | snp | G/T | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109523987 | TCCCAGGGAATTGTG[G/T]TGGACGTGCCATTTG | 89910 |
rs747461682 | snp | G/T | 3.30028e-05 | 0.00406205 | intron-variant | UBE3B | GRCh38.p7 | 12:109498228 | CGGTCTGCTATTCTT[G/T]GCAGCGCCTCACTGT | 89910 |
rs747470546 | snp | A/G | 6.7974e-05 | 0.00582944 | intron-variant | UBE3B | GRCh38.p7 | 12:109533693 | TCAGAGCCAAGTGAG[A/G]AGGGCCCCACAGTTC | 89910 |
rs747512672 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484914 | GGTGTGTGCCACCAT[A/G]CACAGCAAGTTTTTG | 89910 |
rs747557488 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497656 | CTGGACCATCACTGA[A/C]TTGTCCATTTCCCCA | 89910 |
rs747561690 | snp | A/G | 1.69758e-05 | 0.00291335 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483698 | CTGTCGGAGTCGACT[A/G]CAGAGAGATATCAGG | 89910 |
rs747564887 | snp | A/G | 3.29788e-05 | 0.00406058 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524104 | TTCTATAAAAACCTC[A/G]CCTCCATCAAGGTGA | 89910 |
rs747578527 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489125 | AAGTAGCCCATACAT[G/T]CCAGATGCCTCTAGG | 89910 |
rs747593694 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498305 | GACCAAGATCGATGC[C/T]GTGATGTATGTGAAA | 89910 |
rs747605088 | snp | C/T | 3.29919e-05 | 0.00406138 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491055 | TTCAGATATTGTTAA[C/T]CCGTGGCCTGGCAAG | 89910 |
rs747642763 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485443 | AGGTGAACCTCATCT[G/T]ACAGAGAAGGAAACT | 89910 |
rs747664467 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505558 | ATTGTGAGAGTTCCA[C/T]ATTCTTGGGTGTGTT | 89910 |
rs747672997 | in-del | -/TTA | 1.64779e-05 | 0.00287031 | intron-variant | UBE3B | GRCh38.p7 | 12:109488559 | TTAATCTTGCTGTGT[-/TTA]TTGTTTCCAGCCTGA | 89910 |
rs747762235 | in-del | -/G | 1.67136e-05 | 0.00289076 | intron-variant | UBE3B | GRCh38.p7 | 12:109507752 | TAGGTTGACTGCTGT[-/G]GGACTGAATTCCTTT | 89910 |
rs747778462 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517815 | GTGGCCAGATAGCCA[C/T]CCCCACCAGCAGATG | 89910 |
rs747781423 | snp | A/G/T | 6.5895e-05 | 0.00573967 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521184 | CAGCTCTCCCAGCAC[A/G/T]CCATGAAGGGGGTCA | 89910 |
rs747794226 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528682 | AACATGGTGAAACTC[C/T]GTCTCTACTAAAAAT | 89910 |
rs747815389 | snp | A/G | 0.000126976 | 0.00796693 | intron-variant | UBE3B | GRCh38.p7 | 12:109533718 | CAGTTCTCACGGCAG[A/G]AGAACCAGCCAGCCC | 89910 |
rs747815860 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503782 | TTTTAGGTTGCAGCA[A/C]AGTTGTTGTTATGAA | 89910 |
rs747834266 | snp | C/T | 1.65116e-05 | 0.00287324 | intron-variant | UBE3B | GRCh38.p7 | 12:109483855 | TTTTTGCACTTTCTT[C/T]TCTAGGAGAGAGATT | 89910 |
rs747886893 | snp | A/G | 1.6888e-05 | 0.00290581 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499800 | TGGTTCTCCCAATCT[A/G]TGGATTATGGGTGAG | 89910 |
rs748088079 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524679 | GGAGGGCCCCCTCCT[A/T]TCCTTCCCAGTTGAC | 89910 |
rs748136642 | snp | C/T | 8.57082e-05 | 0.00654574 | intron-variant | UBE3B | GRCh38.p7 | 12:109490154 | TCCTCTTCTTCCTTC[C/T]CCTGCCTTGTCTCAC | 89910 |
rs748147684 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500929 | AGGTGACAGCAGATT[C/T]CAGGAAGTTGAGGGA | 89910 |
rs748153144 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478761 | ACTCCAGCCTGGGCA[A/G]CAAAGTGAGACTCCG | 89910 |
rs748196238 | snp | C/G | 1.69186e-05 | 0.00290844 | upstream-variant-2KB, splice-donor-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477259 | GCACCGCCCTCCCTA[C/G]CATGAAAAGTCGGAG | 89910 |
rs748196468 | snp | C/G | 1.72952e-05 | 0.00294063 | intron-variant | UBE3B | GRCh38.p7 | 12:109501586 | CTTGGCTGAAGTACA[C/G]CTCCTGTTTCTTCCT | 89910 |
rs748236573 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540597 | CATGGCAGTGGCCAC[C/T]GAGTAAAGGAAGACA | 89910 |
rs748279232 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109530634 | CTCCGACTTCACACC[A/G]GATGAGAGAGCTATG | 89910 |
rs748313609 | in-del | -/TTG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515365 | ATTATTACTGTTTTT[-/TTG]TTGTTGTTGTTGTTG | 89910 |
rs748334287 | snp | A/G | 5.16151e-05 | 0.00507985 | intron-variant | UBE3B | GRCh38.p7 | 12:109521407 | CCTTGCAAGGCACTT[A/G]ACCTCTGCCTCTCCC | 89910 |
rs748358729 | snp | C/T | 1.64898e-05 | 0.00287135 | intron-variant | UBE3B | GRCh38.p7 | 12:109497769 | GTTGTGCTTTTGTTC[C/T]GGATGCACACGGAGA | 89910 |
rs748359838 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541123 | AGACCATGTTCCAGC[A/G]TGGTCCACCTGCCTG | 89910 |
rs748371643 | snp | A/C/T | 9.10861e-05 | 0.00674806 | intron-variant | UBE3B | GRCh38.p7 | 12:109499610 | TGTCTGGGCCCATCA[A/C/T]ACTCAGCCTTCTCTC | 89910 |
rs748405786 | snp | C/T | 1.73549e-05 | 0.0029457 | intron-variant | UBE3B | GRCh38.p7 | 12:109484015 | ACATGTATAATACTT[C/T]CATATGTCAGATCTT | 89910 |
rs748411631 | snp | A/G | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497847 | CACAGTTCTCAGACA[A/G]TCTGATTCGGCCGTT | 89910 |
rs748446094 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488284 | CAGGCAGGCACATGT[A/G]CATACAGCAAGCCAG | 89910 |
rs748467518 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478336 | GAGCCCTGGATCTTG[A/T]TTGTTTTACTTAGTG | 89910 |
rs748573703 | snp | C/T | 3.32182e-05 | 0.00407529 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511219 | GGATCTCAAACCTAG[C/T]GTGCTCTTCCAAGAA | 89910 |
rs748579047 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520576 | GAAAGATCTGACAGA[A/C]AGTCAGCCCTGTTAC | 89910 |
rs748582198 | snp | C/T | 3.30775e-05 | 0.00406665 | intron-variant | UBE3B | GRCh38.p7 | 12:109524145 | GTGGGTGAGCTAAGC[C/T]GAGCACTGGTGTGAA | 89910 |
rs748598136 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488623 | TACCTCACGATGCTT[A/G]TCACCTTCACAGACA | 89910 |
rs748637278 | snp | C/T | 9.90884e-05 | 0.00703807 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524482 | CCTGACGCTGTCTTA[C/T]GACGAGGACGTCATG | 89910 |
rs748648057 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486309 | CTATTTTGTCTTTGC[A/G]TTTAGTGTTAAAATA | 89910 |
rs748649242 | in-del | -/GA | 1.70478e-05 | 0.00291952 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477301 | CTCCAAACCCGGACT[-/GA]GAGAGGCAGGAAACA | 89910 |
rs748682278 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537738 | TTGAGATGGAGTCTC[A/G]CTGTCGCCCAGGTTG | 89910 |
rs748711749 | snp | C/T | | | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511303 | CATCCCTCACAAAAA[C/T]GTGAGTTGCACTCAG | 89910 |
rs748760399 | snp | A/G | 3.34829e-05 | 0.00409149 | intron-variant | UBE3B | GRCh38.p7 | 12:109483989 | ATAATGAGGTAAAAC[A/G]ATAATAGCAAACATG | 89910 |
rs748791009 | in-del | -/ACG | 1.65105e-05 | 0.00287315 | cds-indel, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524481 | GCCTGACGCTGTCTT[-/ACG]ACGAGGACGTCATGG | 89910 |
rs748814658 | snp | A/G | 0.000198666 | 0.0099646 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507723 | TCTGTGACTGTTCGC[A/G]GCACCTCATCACGTA | 89910 |
rs748859849 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527587 | TTAGACTGTCAGAAA[C/T]GTCAGGAGAACAGAC | 89910 |
rs748892701 | snp | A/T | 1.71187e-05 | 0.00292559 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534603 | CAGGACACCGGGGAC[A/T]CTCTGGGCAGCGTCC | 89910 |
rs748898698 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542613 | GGTGGGACCCTAATC[C/T]GATGTGACTGGTGTC | 89910 |
rs748916432 | snp | A/G | 1.651e-05 | 0.0028731 | splice-donor-variant | UBE3B | GRCh38.p7 | 12:109498354 | CGCTTTGTCTAATGG[A/G]TAAGTATCCGTGGCT | 89910 |
rs748948510 | snp | A/C | 1.65222e-05 | 0.00287417 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509642 | CAGATTTCATTCAAA[A/C]TGGAAGAGCTGGTCA | 89910 |
rs748948860 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514559 | ATGTAACTCGCCTTC[C/T]GCCTGTGTATCACCA | 89910 |
rs748971736 | snp | A/G | 0.0001812 | 0.00951667 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488644 | TTCACAGACACTTCA[A/G]CGTGGAAAATTCTTC | 89910 |
rs748985642 | snp | A/G | 1.65244e-05 | 0.00287436 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524486 | ACGCTGTCTTACGAC[A/G]AGGACGTCATGGGTC | 89910 |
rs749006235 | in-del | -/T | | | frameshift-variant | UBE3B | GRCh38.p7 | 12:109543538 | CTCCAGGAGCCACAC[-/T]TTTAAGAAGGATGCA | 89910 |
rs749093015 | in-del | -/TT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482767 | GATTTAGATAAAAAC[-/TT]AGTATATAATTTAGA | 89910 |
rs749095735 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533061 | CGCCCTCACCGTCTC[C/G]CATTTTCTCCTCACA | 89910 |
rs749157533 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530041 | CGTCTCATCTCTGGC[A/G]ACAATGCTGAGATTG | 89910 |
rs749193019 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521196 | CACGCCATGAAGGGG[A/G]TCATCCGTGTGAAGT | 89910 |
rs749211880 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505048 | TCTCCTGTGTGTCCA[C/G]CTTTTTAAATGAGCT | 89910 |
rs749212032 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491200 | GTTTTTCTTTCTCTC[A/G]TTACTGGTATTAGGT | 89910 |
rs749220992 | snp | A/G | 1.65674e-05 | 0.00287809 | intron-variant | UBE3B | GRCh38.p7 | 12:109521102 | CCCCGAATTGTGTGC[A/G]TAAGGCTTTGGGCTT | 89910 |
rs749221306 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533916 | CAGGAGGCAGGCAGG[C/T]GCAGACTCGAATGCT | 89910 |
rs749221416 | snp | C/T | 1.65315e-05 | 0.00287498 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491163 | GAGGTGTTGGCATGT[C/T]CTTGAATGCTTCCTC | 89910 |
rs749275521 | in-del | -/TGTT | 5.12282e-05 | 0.00506078 | intron-variant | UBE3B | GRCh38.p7 | 12:109510326 | CTCCTCTGACTTTCC[-/TGTT]TGTTTGTCCCACAGA | 89910 |
rs749282936 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481342 | AGGAAAATGTCAAAT[A/G]TAATTTTCAGTAGCT | 89910 |
rs749290531 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480334 | ATTATCAACCTCTAA[A/G]CCAATTAATAGATGA | 89910 |
rs749323192 | snp | A/G | 4.94189e-05 | 0.00497062 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497856 | CAGACAATCTGATTC[A/G]GCCGTTCCTCATCCA | 89910 |
rs749443443 | snp | G/T | 1.71678e-05 | 0.00292978 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521517 | TGCAGCTCTTCGAGT[G/T]TGTGGGGAAGATGCT | 89910 |
rs749455719 | snp | C/T | 1.64887e-05 | 0.00287125 | intron-variant | UBE3B | GRCh38.p7 | 12:109497773 | TGCTTTTGTTCTGGA[C/T]GCACACGGAGACCTG | 89910 |
rs749457639 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497921 | AGCACAGTGACCCCT[A/G]AGGTAAGCAGGCTCT | 89910 |
rs749472819 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539637 | CATCTATGAGCCATC[A/G]ATGACTCATGGCTGT | 89910 |
rs749509059 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511107 | TGAGAAACAGACAGC[A/G]CCCTGCATGTGGCCC | 89910 |
rs749513015 | snp | C/G | 1.64795e-05 | 0.00287045 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486525 | CTCCTTTGGATTCAA[C/G]AGATCAAGAACATTT | 89910 |
rs749549306 | snp | A/G | 1.65625e-05 | 0.00287766 | intron-variant | UBE3B | GRCh38.p7 | 12:109523954 | TCCTGGCTGATGGAC[A/G]GCTCTGCTTCTCTGC | 89910 |
rs749557894 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109499494 | CACACAGCAGCCTCC[A/G]GCATTGACAGGTGCC | 89910 |
rs749558915 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522708 | AAACAGTCTATGTGC[A/T]CCGGCCTCAGTCCCT | 89910 |
rs749563584 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109498546 | AAATATTCCAGCCTG[A/G]CAAACTAGTTAAGTG | 89910 |
rs749597781 | snp | A/G | 0.000115366 | 0.00759405 | intron-variant | UBE3B | GRCh38.p7 | 12:109489886 | CACATTATGGCAAGA[A/G]ACTTTTTTGTTCTCA | 89910 |
rs749613721 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486947 | AGCAAGGAAGAGAAC[A/G]TTGTGCTCTAGAATA | 89910 |
rs749615757 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512585 | TCTATTTTCTTTTTC[-/T]TTTTTTTAACGAAGT | 89910 |
rs749669361 | in-del | -/GTTTGCAAACAT | 3.58064e-05 | 0.00423106 | cds-indel, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483542 | GCAGGGTTTGTGCAA[-/GTTTGCAAACAT]GTTCACCCTGTCTCA | 89910 |
rs749686366 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109526372 | GCTTGTTTGCCATGA[A/G]CTGATTCCTGGAGGG | 89910 |
rs749720246 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109530263 | ATTAAGAAGTGGAAG[C/G]AGGCCTGAGGACTGG | 89910 |
rs749721290 | in-del | -/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109537042 | TTTTTTGAGATGGGG[-/T]TTTTGCCATGTCACC | 89910 |
rs749737746 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518984 | TCATGCTCTCCTGGG[C/T]ATTGTTTCCTTTTTT | 89910 |
rs749739500 | snp | A/T | 1.68772e-05 | 0.00290488 | intron-variant | UBE3B | GRCh38.p7 | 12:109511313 | AAAAACGTGAGTTGC[A/T]CTCAGAGCTGGGCCC | 89910 |
rs749752343 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510881 | ATAGGCATGTATCTG[C/T]ATTTTTATCAATGAG | 89910 |
rs749754231 | snp | A/G | 1.69582e-05 | 0.00291184 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477272 | TACCATGAAAAGTCG[A/G]AGGACGCAGGAGTCT | 89910 |
rs749755560 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486862 | ATGATCTACATTATT[-/A]TACTAGTCAGGCCTC | 89910 |
rs749759238 | in-del | -/AAAAAAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486581 | GCAGCTCAAGGTAAC[-/AAAAAAA]AAAAAAAAAAAAAAA | 89910 |
rs749794174 | snp | C/G | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475572 | TGCGGAGGGGTGGCT[C/G]ATCAGTCACTAGTGT | 89910 |
rs749832440 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520404 | AGTTGTGGTTCTGGG[G/T]CTGTGCATGTTGAGG | 89910 |
rs749845480 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503075 | CCGGAATATTCTCAG[G/T]CCTGTCGGGGGTAAA | 89910 |
rs749845957 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477183 | ACCCCCTCCTCTCGG[C/T]CCCTTCTTATACTCT | 89910 |
rs749860136 | snp | C/T | 5.18453e-05 | 0.00509116 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483574 | CCCTGTCTCAGACCT[C/T]GAGAGCATGGTTCAT | 89910 |
rs749899539 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478182 | CAGGTTTCACAGAGG[G/T]TGTGAATACGTTTTA | 89910 |
rs749905472 | snp | C/T | 1.65056e-05 | 0.00287272 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486474 | TCCCACCTATAGGTG[C/T]GGTATGTGTCCCTGG | 89910 |
rs749946688 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515035 | CTCCTGCCTCAGCCT[-/C]CCCGAGTAGCTGGGA | 89910 |
rs749950650 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479597 | TTAGCAAAATAAGTA[C/T]TTAATAAACACTTGA | 89910 |
rs749998401 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538506 | GAATCTTGATGTCCC[C/T]TCCAGAGCACGTGAG | 89910 |
rs750030747 | snp | C/T | 1.69006e-05 | 0.00290689 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534691 | CCACCTGCTTCAACC[C/T]GCTCAAGCTGCCCAA | 89910 |
rs750076941 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522467 | TGGCCTTCGCAGTGG[G/T]CTCCAGAGCTGCAGG | 89910 |
rs750087592 | snp | A/C | 1.65222e-05 | 0.00287417 | intron-variant | UBE3B | GRCh38.p7 | 12:109501321 | GTGGGCTGGCCCTGG[A/C]CCTGCATCAGATGGA | 89910 |
rs750128681 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516786 | CTACTGTTTCGAACC[A/G]TGGTTACCAAGGAGA | 89910 |
rs750132011 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509734 | GAGAAAAGGTGTCTG[C/T]TGTTGTTTGGTTGAT | 89910 |
rs750143964 | snp | C/T | 3.89978e-05 | 0.00441558 | intron-variant | UBE3B | GRCh38.p7 | 12:109510504 | GAAGCCAGCCTGCTC[C/T]GGCACGCTGCCCGAG | 89910 |
rs750163727 | snp | C/T | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503034 | CCAGGTCTCCTAAAG[C/T]GTGCTTTTCAAAAGT | 89910 |
rs750166728 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527337 | TAAAACAGTGGAGCC[G/T]GGCATGAGAAGCAGA | 89910 |
rs750209617 | snp | A/C | 5.11356e-05 | 0.0050562 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477295 | AGGAGTCTCCAAACC[A/C]GGACTGAGAGAGGCA | 89910 |
rs750250486 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485348 | CTCTACGCTCATGGA[A/G]CTCATAGCCCAGCAA | 89910 |
rs750296240 | snp | C/T | 1.64904e-05 | 0.00287139 | intron-variant | UBE3B | GRCh38.p7 | 12:109533434 | AGAGCAGGAGCCTGC[C/T]CCGTCCCCACTGACC | 89910 |
rs750357911 | in-del | -/CAAGGCTGGGAG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511735 | GACAGCCTTAGAAAC[-/CAAGGCTGGGAG]CAAGGGCTTTCTGCA | 89910 |
rs750360001 | snp | C/T | 4.94197e-05 | 0.00497066 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503147 | TGTCCTCTACCAGAC[C/T]TCGCTGACAACTCTC | 89910 |
rs750360032 | snp | C/T | 1.64735e-05 | 0.00286993 | stop-gained, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497834 | CCTGTGATTGCTGCA[C/T]AGTTCTCAGACAATC | 89910 |
rs750397701 | snp | A/G | 3.29728e-05 | 0.00406021 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533509 | TCCTGGGATTCGCCT[A/G]CCTCAAGCCTCCATT | 89910 |
rs750400885 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517527 | CGTGCCTCCAATCTG[C/T]TGGAACATGGTTGTC | 89910 |
rs750401530 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109543505 | CTCACACCCTACCTG[G/T]AATCGATCCTTTGTT | 89910 |
rs750407419 | snp | C/T | 1.71764e-05 | 0.00293051 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521500 | CATCCATGAGAATTA[C/T]CTGCAGCTCTTCGAG | 89910 |
rs750411366 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497892 | TGTCTGTGCCTGCTC[C/T]GGTGACTCATCTCAG | 89910 |
rs750469973 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483896 | TTAAAGCAGATGACC[C/T]TGAGTCCACTAAAAG | 89910 |
rs750517597 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522404 | CCTTGGGAGAGTCCT[C/G]TTTCCCAGGAGGAAG | 89910 |
rs750519425 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109492202 | TGGTCTAGACTGTGC[C/T]TTCCACTAACCACTA | 89910 |
rs750608824 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542789 | AGGAACCAACCCTGT[C/G]AATCTCTTGATTTCA | 89910 |
rs750638203 | snp | C/T | 0.000193367 | 0.00983089 | intron-variant | UBE3B | GRCh38.p7 | 12:109533867 | CCAGGGCTCCAGATC[C/T]GAGGCAGCATGGGAG | 89910 |
rs750639710 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505985 | GGCATTTCAGATCCA[A/G]CCTTTCTAAGTCAAG | 89910 |
rs750656809 | snp | C/T | 1.68425e-05 | 0.00290189 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534660 | CGGGAGCCAGGCGGC[C/T]GCCTGCCCACCTCCT | 89910 |
rs750662403 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493652 | ACCTTTTAAAGTAAG[A/G]TATCAGTGGTTTCAT | 89910 |
rs750663891 | snp | A/T | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524446 | ACATTAGCGCTATGA[A/T]GGGGACATCACTGAC | 89910 |
rs750665433 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498296 | TTTTTAAGAGACCAA[C/G]ATCGATGCCGTGATG | 89910 |
rs750697452 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511050 | AAGCTGCCATAGGCT[A/T]TACATGTATGAATGA | 89910 |
rs750701232 | snp | G/T | 1.75708e-05 | 0.00296397 | intron-variant | UBE3B | GRCh38.p7 | 12:109490061 | CCAACACCTGCACTT[G/T]GATTTTTACATTTGC | 89910 |
rs750706247 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524231 | CTGTAGCTGCTACAG[A/G]CCCCTCACATCCCCC | 89910 |
rs750717595 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482038 | AGGCTTGCACCAACT[G/T]TTTTTTGGTTATAAA | 89910 |
rs750718180 | in-del | -/CT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541086 | CCTGGGGCCTCTAGC[-/CT]CAAACCACTGCTGCA | 89910 |
rs750728353 | snp | A/G | 2.42568e-05 | 0.0034825 | intron-variant | UBE3B | GRCh38.p7 | 12:109499592 | GGGAGGCACCAAAAT[A/G]TTTGTCTGGGCCCAT | 89910 |
rs750753894 | snp | C/T | 3.29837e-05 | 0.00406088 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501377 | CTCTCCTAGCCTTAA[C/T]GAGTCAATGCACTTG | 89910 |
rs750759209 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524927 | AGCAGAGACCCTGGT[C/T]TCAGGGCCGCAGCAC | 89910 |
rs750801159 | snp | A/G | 1.68707e-05 | 0.00290432 | intron-variant, missense, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491009 | ATGAATATAAAGTTG[A/G]TATCATCCTCTGACC | 89910 |
rs750817238 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482867 | GGCAGGATGGTAATT[A/G]TAAGGACAATGGAAT | 89910 |
rs750821474 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500239 | CAAGAGGTGGAATAT[A/G]AATTTTTAAAAGTGT | 89910 |
rs750827971 | in-del | -/AG | 1.64738e-05 | 0.00286995 | frameshift-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521290 | TGGAAGAGATCATCA[-/AG]AGAGTTTTTGACCCA | 89910 |
rs750907029 | snp | G/T | 1.65299e-05 | 0.00287483 | intron-variant | UBE3B | GRCh38.p7 | 12:109530084 | TAAAGTAAGAGGCGG[G/T]TGGGGGGAAGGGTGA | 89910 |
rs750913398 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540367 | TGTGCATCACCACAA[C/G]CGGCTAGTTTATTTT | 89910 |
rs750938326 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512017 | TGGCTTGGGTACTTG[C/G]GGGGTGTTTTCCTGA | 89910 |
rs750962414 | in-del | -/CTG | 1.74708e-05 | 0.00295552 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534585 | GCCACGATGTGTGCC[-/CTG]TTCAGGACACCGGGG | 89910 |
rs750988480 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109499279 | TATAATATTAAAATG[C/T]AACACTAACTAAATA | 89910 |
rs750995160 | snp | C/T | 1.71126e-05 | 0.00292506 | intron-variant | UBE3B | GRCh38.p7 | 12:109507546 | CCTGAAGCTTGGGTT[C/T]CTCTGTGTTTTTTCC | 89910 |
rs751045596 | snp | C/T | 0.000181263 | 0.00951834 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510421 | TACGAGCGGGACTGC[C/T]GGCGGCGCTTCACCC | 89910 |
rs751081044 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488789 | GGCCCTGAGACCATA[A/C]AAATGAGGATGCCCT | 89910 |
rs751147219 | snp | G/T | 5.45678e-05 | 0.00522311 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534816 | CTCCAGGGCTCCTGG[G/T]CTGCCAGGGACCTTC | 89910 |
rs751210670 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532200 | GATACTTCTGTGTCT[C/G]TCCCCTTATTCTTAA | 89910 |
rs751218901 | snp | A/C/T | 3.30985e-05 | 0.00406797 | intron-variant, missense, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491037 | ACCAATTAAAACATT[A/C/T]TTTTCAGATATTGTT | 89910 |
rs751254413 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501393 | GAGTCAATGCACTTG[A/G]TCACCAAACAGCTGC | 89910 |
rs751265914 | snp | C/T | 1.73333e-05 | 0.00294386 | intron-variant | UBE3B | GRCh38.p7 | 12:109507516 | GGAGAAATAACAGAC[C/T]AGGTGGAGTCTCCAC | 89910 |
rs751273435 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478098 | TACTGTTCGCTCGCT[C/G]TGTGACCTTGGGTGA | 89910 |
rs751307576 | snp | C/T | 1.65078e-05 | 0.00287291 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501494 | CCAGGAGCCAGCCCA[C/T]GCACAGCCAGCATCC | 89910 |
rs751348475 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508486 | TTTTTAAGCTTATGC[A/C]TCTTGTGTGTTTGGT | 89910 |
rs751361049 | snp | A/G | 1.66112e-05 | 0.00288189 | intron-variant | UBE3B | GRCh38.p7 | 12:109498182 | AAGTTCACTCTCTAC[A/G]GGAAACTGTTTCTGG | 89910 |
rs751378709 | snp | A/G/T | 6.60539e-05 | 0.00574658 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533538 | TTCTCCATCCGCTGC[A/G/T]TGGAGGTGTCGGACG | 89910 |
rs751477806 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538500 | ACACAGGAATCTTGA[C/T]GTCCCCTCCAGAGCA | 89910 |
rs751480328 | snp | A/C/G | 3.49194e-05 | 0.00417836 | intron-variant | UBE3B | GRCh38.p7 | 12:109533623 | TTGTCTGCTGTGCCC[A/C/G]CTGTGCAAGGCCCTT | 89910 |
rs751532958 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527175 | ACGGAGGTCCTTAGA[C/T]ATGGGAATTGGAGAG | 89910 |
rs751547397 | snp | A/C | 3.40745e-05 | 0.00412748 | intron-variant | UBE3B | GRCh38.p7 | 12:109486581 | GCAGCTCAAGGTAAC[A/C]AAAAAAAAAAAAAAA | 89910 |
rs751551547 | snp | A/G | 6.58913e-05 | 0.00573945 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524044 | GGGCACCACCACAGC[A/G]TCTTCTATAGCTCGG | 89910 |
rs751602561 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496685 | CATTTGTGTATCTTC[G/T]TTGGAGAAATGTATG | 89910 |
rs751692219 | snp | C/G | 1.64914e-05 | 0.00287149 | intron-variant | UBE3B | GRCh38.p7 | 12:109488719 | ACATTTCCATAGAGA[C/G]CTCAGGGACCTTTTT | 89910 |
rs751728714 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517461 | AGATAGGTACCCAGT[C/T]CTCATATGTCAGAAA | 89910 |
rs751748843 | in-del | -/AACA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486578 | CAAGCAGCTCAAGGT[-/AACA]AAAAAAAAAAAAAAA | 89910 |
rs751750924 | snp | A/G | 0.000115108 | 0.00758556 | intron-variant | UBE3B | GRCh38.p7 | 12:109533713 | CCCCACAGTTCTCAC[A/G]GCAGGAGAACCAGCC | 89910 |
rs751777398 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504695 | GCAGGTTTCCCAAAG[A/G]TGAGCAGAGGGAGGA | 89910 |
rs751783439 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | UBE3B | GRCh38.p7 | 12:109526325 | TTCCCCATTAGAGTC[C/T]TCCCTATTAATTACT | 89910 |
rs751799524 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502635 | AGGTTGTCACGCCTT[A/G]CTTCCCTCTAAAGGC | 89910 |
rs751799891 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505253 | TTTCTACTGACAACT[G/T]AGGAAGTGTCTGTTT | 89910 |
rs751800469 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109543338 | CCAGAAACCAGCCTC[A/G]TGCAGACAGGCTCCA | 89910 |
rs751840457 | snp | C/T | 1.85262e-05 | 0.00304348 | intron-variant | UBE3B | GRCh38.p7 | 12:109511349 | TGTCTTTCTATTCCC[C/T]CACGTGGTTCCTGCC | 89910 |
rs751856076 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521163 | GACGGCTACGAGCAG[C/G]TTAGGCAGCTCTCCC | 89910 |
rs751856458 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530561 | GGAAGCACACAGTCT[A/G]CTACGGTGGTTTCCA | 89910 |
rs751875776 | snp | A/C | | | stop-gained, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490521 | TTCCTGATTTGGTTT[A/C]ATATGCTCCTCACAA | 89910 |
rs751887905 | snp | C/T | 4.94222e-05 | 0.00497078 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109489969 | GCAAATATAATGGGA[C/T]ATCTCAACCAGCATG | 89910 |
rs751986014 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493542 | ATGTATTAGATTCCA[C/T]TGAATCACTTGTTAA | 89910 |
rs752047709 | snp | A/G | 5.17023e-05 | 0.00508414 | intron-variant | UBE3B | GRCh38.p7 | 12:109509561 | CTTCGCCTTTTTTCA[A/G]TGTGGAATTGTGGGT | 89910 |
rs752095625 | snp | C/T | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524011 | CCATTTGCATCCTTC[C/T]TCCTGAGCCAACTGC | 89910 |
rs752097347 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507701 | CTCTTGGCCATGCTG[A/G]TGCTGTTCTGTGACT | 89910 |
rs752104283 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510776 | AGAGTTAAAAGGCAG[C/T]TTTTATTAGCAGAAT | 89910 |
rs752138708 | in-del | -/GT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515365 | TTATTACTGTTTTTT[-/GT]TGTTGTTGTTGTTGT | 89910 |
rs752149260 | snp | A/G | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498275 | ATGCTTCGTAAATTC[A/G]TCATATTTTTAAGAG | 89910 |
rs752173846 | snp | C/T | 1.691e-05 | 0.0029077 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477217 | GCTGCCCAGCTCCCT[C/T]GGCCGCCCTCAACCC | 89910 |
rs752174375 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481803 | TCAGAAGATGGCTAC[C/T]GTTTCTCTCCAAGCC | 89910 |
rs752191578 | snp | G/T | 1.66142e-05 | 0.00288216 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501529 | AGAATGTGCTCCCAG[G/T]GAAGAGTGAGTGACG | 89910 |
rs752213664 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540120 | CGTTCATTCTGCTGC[C/T]GAAGTCTTCTGCTCC | 89910 |
rs752272938 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530588 | TCCATGGAAGTCACA[A/G]AGTCATCATCTGGCT | 89910 |
rs752287117 | snp | G/T | 1.65081e-05 | 0.00287293 | intron-variant | UBE3B | GRCh38.p7 | 12:109502990 | GGCAGCTGGCTGAGC[G/T]GCTGCTCACATGTCT | 89910 |
rs752322235 | snp | A/G | 3.31016e-05 | 0.00406813 | intron-variant | UBE3B | GRCh38.p7 | 12:109530095 | GCGGGTGGGGGGAAG[A/G]GTGAAATTCCTTGGC | 89910 |
rs752371397 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540930 | GGCTCTGGGACCCAC[A/G]CAAGAAGTGCGGTGG | 89910 |
rs752372545 | snp | A/G | | | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530038 | CAGCGTCTCATCTCT[A/G]GCGACAATGCTGAGA | 89910 |
rs752381933 | snp | A/G | 1.64846e-05 | 0.0028709 | splice-donor-variant | UBE3B | GRCh38.p7 | 12:109521325 | CTCAATCTGTTCAAG[A/G]TATTTAAGGGGAGCA | 89910 |
rs752383193 | snp | A/G | 4.94246e-05 | 0.0049709 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498278 | CTTCGTAAATTCATC[A/G]TATTTTTAAGAGACC | 89910 |
rs752385010 | in-del | -/CAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481411 | ATCACAGCTGTAATT[-/CAA]CAACAACTTTGGGAT | 89910 |
rs752392755 | snp | C/T | 1.64958e-05 | 0.00287187 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491126 | TTTTCTCTAGCGTTA[C/T]GGTGAGTAAGAAACC | 89910 |
rs752425436 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518517 | CCCAATTGTGTGGTA[A/G]GGACTCCCTTTCTAG | 89910 |
rs752442109 | in-del | -/AG | 3.59357e-05 | 0.0042387 | intron-variant | UBE3B | GRCh38.p7 | 12:109521570 | GGAACGTTAAGAAAC[-/AG]AGAAATGTAAAATAA | 89910 |
rs752444128 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | UBE3B | GRCh38.p7 | 12:109497811 | GAGTGGATCTATCTG[C/T]GTCTAGCCCTGTGAT | 89910 |
rs752474667 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484651 | CGCCTCAGCCTCCCA[C/G]AGTGCTGGGATTACA | 89910 |
rs752489808 | snp | A/G | 1.86698e-05 | 0.00305525 | intron-variant | UBE3B | GRCh38.p7 | 12:109486599 | AAAAAAAAAAAAAAA[A/G]AAAAGCAAAACCAGA | 89910 |
rs752551850 | snp | A/G | 3.29484e-05 | 0.00405871 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524058 | CGTCTTCTATAGCTC[A/G]GTGGATGAACTGCCT | 89910 |
rs752552812 | snp | C/T | 1.92565e-05 | 0.00310288 | intron-variant | UBE3B | GRCh38.p7 | 12:109511176 | TTCCTTCTTTTAATT[C/T]TCCCAAACCCATGTC | 89910 |
rs752569056 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507273 | TTTCTGTGCTTCAGT[C/T]TCCTCCTGTATAAGA | 89910 |
rs752604839 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524439 | CTCTGTTACATTAGC[A/G]CTATGATGGGGACAT | 89910 |
rs752606144 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501409 | TCACCAAACAGCTGC[A/G]GTTCTTGTGGGGGGT | 89910 |
rs752671363 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109489997 | ATGGATTTTATTCTG[C/T]GCTGCAGGTCTGTGA | 89910 |
rs752725248 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508420 | TACTTAGTGCAGTGC[C/T]TGGCACAGAGTGGGA | 89910 |
rs752731691 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483234 | GACTGATTCATTCTT[C/T]GTTCATTCGTAAAGC | 89910 |
rs752760779 | snp | C/T | 0.000198824 | 0.00996856 | intron-variant | UBE3B | GRCh38.p7 | 12:109529846 | GGTGACAGCCTGCCC[C/T]GTCCTGTTAATTGTC | 89910 |
rs752798164 | in-del | -/CC | 3.30101e-05 | 0.00406251 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491140 | ACGGTGAGTAAGAAA[-/CC]ATAGCTGAGGTGTTG | 89910 |
rs752815009 | in-del | -/AAAAAAAAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486581 | GCAGCTCAAGGTAAC[-/AAAAAAAAA]AAAAAAAAAAAAAAG | 89910 |
rs752829020 | snp | C/T | 6.69053e-05 | 0.00578344 | intron-variant | UBE3B | GRCh38.p7 | 12:109490044 | TGCAACTTCTCCACT[C/T]TCCAACACCTGCACT | 89910 |
rs752830444 | snp | A/C | 1.80595e-05 | 0.0030049 | intron-variant | UBE3B | GRCh38.p7 | 12:109483507 | CAACAATCTACAACA[A/C]CCACTTGCCCATTTT | 89910 |
rs752846938 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527068 | GAAAGACACCTTGGC[A/G]GGGAGGGGCAGATCA | 89910 |
rs752871728 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542089 | AGTGTGGCAGGAGGT[A/G]ATTCTTCATGCCATG | 89910 |
rs752904633 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516883 | GGTCCAGGATGCTGG[A/G]GGTGAGTGTGAAGCC | 89910 |
rs752918068 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532515 | GACAGCTTGATGATG[-/T]TAAGTGACAAGCCCC | 89910 |
rs752922530 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527528 | CATCATGTTCCTCTC[A/G]GATCAGGTGGTTCAG | 89910 |
rs752947844 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513673 | TTTTAAGTCCAGGGT[A/G]TATAGTAATCCCCAC | 89910 |
rs753003633 | snp | C/T | 1.66991e-05 | 0.00288951 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509610 | GAATCCTTGATGACA[C/T]TGAAGTTTATGAAGA | 89910 |
rs753065516 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502370 | TCAGTAATGGGTTCC[A/G]TGGGAAGGTTCTCGT | 89910 |
rs753070117 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526585 | ATTGTATTAAATTCA[A/G]TTTGCGGCCGGGCAC | 89910 |
rs753118621 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109490341 | ATATTTCTAGCTCTG[C/T]GTCCTCAAACAGCCC | 89910 |
rs753126281 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532411 | CTTTTTTTGATGCCC[A/G]ACACACATAAACTGT | 89910 |
rs753126557 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518703 | CTCCCTTCACAAATA[C/T]CATTGCTTATTGGAA | 89910 |
rs753179139 | snp | C/T | 5.21127e-05 | 0.00510428 | intron-variant | UBE3B | GRCh38.p7 | 12:109521423 | ACCTCTGCCTCTCCC[C/T]GTCTTTTTGCCTTGC | 89910 |
rs753193373 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479915 | TCTAATTCCATGGAC[C/G]CTCTGCCATTGAGGC | 89910 |
rs753221661 | snp | A/G | 0.000148374 | 0.00861191 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533505 | CCGCTCCTGGGATTC[A/G]CCTACCTCAAGCCTC | 89910 |
rs753230600 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522649 | GGAGGTCTCAGGGCC[A/G]AACTCCTTTCACTCT | 89910 |
rs753230950 | snp | A/G | 1.76281e-05 | 0.0029688 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534579 | ATTCAAGGCCACGAT[A/G]TGTGCCTTCAGGACA | 89910 |
rs753244272 | snp | C/G | 2.06222e-05 | 0.00321102 | intron-variant | UBE3B | GRCh38.p7 | 12:109499627 | CTCAGCCTTCTCTCT[C/G]TGTAGGCAACCTCCT | 89910 |
rs753254006 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480738 | TGACTCCCAAAGCCC[A/G]TGTGCCCCTCACTGT | 89910 |
rs753282061 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant | UBE3B | GRCh38.p7 | 12:109526349 | AATTACTCCCATCTT[C/T]TCCCCCAGCTTGTTT | 89910 |
rs753285450 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523917 | CACCCTGAGCCACCC[C/G]AATCCAAACACTGCA | 89910 |
rs753307359 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479748 | AATAACATTGCTGAA[A/G]GGATAATAATCTCAA | 89910 |
rs753310808 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491862 | GCTATGCTAGCAGGA[C/T]CCCATGGGCTTATTT | 89910 |
rs753407105 | snp | C/G | 1.73189e-05 | 0.00294264 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521470 | TGAGAGGCTGTACCC[C/G]TCACCCACATCCTAC | 89910 |
rs753431891 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497541 | TGTATATAGTTTTTC[A/G]TCTTGCCTTTTTTTA | 89910 |
rs753450646 | snp | A/G | 1.65029e-05 | 0.00287248 | intron-variant | UBE3B | GRCh38.p7 | 12:109521346 | AAGGGGAGCAACAGC[A/G]GGGCTGACAGCAGCC | 89910 |
rs753464361 | snp | C/G | 0.000201593 | 0.0100377 | intron-variant | UBE3B | GRCh38.p7 | 12:109510327 | TCCTCTGACTTTCCT[C/G]TTTGTTTGTCCCACA | 89910 |
rs753509600 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529663 | TTGGGGAGGAGTGAA[C/T]GATGCAGTGCCCTCA | 89910 |
rs753548932 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528739 | GGCGCTGTAATGTCA[C/G]CTCAGGAGACTGAGG | 89910 |
rs753562673 | snp | A/G/T | 3.29713e-05 | 0.00406015 | intron-variant | UBE3B | GRCh38.p7 | 12:109526316 | AAGCTTTATTTCCCC[A/G/T]TTAGAGTCCTCCCTA | 89910 |
rs753563565 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539909 | TCATGCTTTTCTTAC[C/T]GTGACAGTCCAAGTG | 89910 |
rs753580359 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109498173 | CAAGTGATCAAGTTC[A/G]CTCTCTACAGGAAAC | 89910 |
rs753585725 | snp | C/T | 1.68932e-05 | 0.00290625 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477226 | CTCCCTCGGCCGCCC[C/T]CAACCCCTAGTCCAT | 89910 |
rs753600156 | snp | C/T | 1.6537e-05 | 0.00287545 | intron-variant | UBE3B | GRCh38.p7 | 12:109486465 | TCCTCTTTTTCCCAC[C/T]TATAGGTGTGGTATG | 89910 |
rs753631624 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486004 | ACCCCCAGTGTGTCT[C/G]TTTGCAGAGATTTGA | 89910 |
rs753643385 | snp | A/T | 1.64781e-05 | 0.00287033 | intron-variant | UBE3B | GRCh38.p7 | 12:109488691 | GGACTTGCTTCAAAA[A/T]GTTCTCTAACCAACA | 89910 |
rs753701231 | snp | A/G | 3.35357e-05 | 0.00409472 | intron-variant | UBE3B | GRCh38.p7 | 12:109501545 | GAAGAGTGAGTGACG[A/G]GAGCAGGCCCAACCC | 89910 |
rs753704881 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518384 | AAATTCAGATCTTCC[A/G]TGTTGTGAACTAATT | 89910 |
rs753761671 | snp | C/T | 3.59984e-05 | 0.00424239 | intron-variant | UBE3B | GRCh38.p7 | 12:109511344 | CGATGTGTCTTTCTA[C/T]TCCCCCACGTGGTTC | 89910 |
rs753826150 | snp | A/G | 3.3432e-05 | 0.00408838 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483667 | TTGTGATCCAGGCCC[A/G]TGTCCGGAGTTTTCT | 89910 |
rs753836842 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530614 | TGGCTCTGGGATATT[C/G]TGGCCTCCGACTTCA | 89910 |
rs753850453 | snp | C/T | 1.64991e-05 | 0.00287215 | intron-variant | UBE3B | GRCh38.p7 | 12:109503009 | GCTCACATGTCTTCT[C/T]TTCTCCATGCCAGGT | 89910 |
rs753878565 | snp | G/T | 0.000140716 | 0.00838679 | missense, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490585 | GTATGACTGGCAGTT[G/T]TCTCGCTAGAGGAAC | 89910 |
rs753892158 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476437 | TCTTTGGTCATCTCT[A/T]CCCAGGGACAATGAG | 89910 |
rs753898522 | snp | A/G | 0.00171442 | 0.0292279 | intron-variant | UBE3B | GRCh38.p7 | 12:109516893 | GCTGGAGGTGAGTGT[A/G]AAGCCTATGGAATCC | 89910 |
rs753911232 | in-del | -/A | 1.66852e-05 | 0.0028883 | intron-variant | UBE3B | GRCh38.p7 | 12:109516904 | GTGTGAAGCCTATGG[-/A]ATCCTACCACAAGGA | 89910 |
rs753923454 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494934 | ACAGCCCTTTGTACC[C/T]TTATAACAATGCAGT | 89910 |
rs753952998 | in-del | -/AGAG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539423 | TCTTACGAGGGCATT[-/AGAG]AGAGCAAGAGCCTCA | 89910 |
rs753969069 | snp | A/C/T | 6.86407e-05 | 0.00585803 | intron-variant | UBE3B | GRCh38.p7 | 12:109483727 | GGTAAGGGCTAGGAT[A/C/T]TCCCTAGCACATGAT | 89910 |
rs753981947 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536724 | CTGCGTTCTGCATTT[C/T]ATTCCGCCATATGCC | 89910 |
rs753992567 | in-del | -/AAAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528850 | ATGAAACTCCATCTC[-/AAAA]AAAAAAAGAAAAGAA | 89910 |
rs754032570 | snp | C/T | 1.65345e-05 | 0.00287524 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533548 | GCTGCGTGGAGGTGT[C/T]GGACGATCAGGTACC | 89910 |
rs754066374 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483049 | TGAATACAATGATGA[C/T]GACAGCAAATAATCA | 89910 |
rs754085940 | snp | C/G | 2.72535e-05 | 0.00369134 | intron-variant | UBE3B | GRCh38.p7 | 12:109533664 | TATCTCAGCAAGGCA[C/G]GCAGCTGGACCCCTC | 89910 |
rs754089343 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524942 | CTCAGGGCCGCAGCA[C/T]GTCTCCTCCCACGGT | 89910 |
rs754099566 | snp | C/T | 1.72791e-05 | 0.00293926 | intron-variant | UBE3B | GRCh38.p7 | 12:109507527 | AGACCAGGTGGAGTC[C/T]CCACCTGAAGCTTGG | 89910 |
rs754140991 | snp | C/G | 1.65026e-05 | 0.00287246 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499726 | AGACGCTGTGCTACT[C/G]TCGGAAGTATGTGTC | 89910 |
rs754144424 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525512 | TGCTGACAGCAGTGG[A/G]ACTGGGATCAGTGTG | 89910 |
rs754195839 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513320 | AGGTGCTGCACAATA[A/T]TTTAAATTTCTGAGG | 89910 |
rs754271889 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541073 | TGCAGCCTTGCGCTC[C/T]TGGGGCCTCTAGCCA | 89910 |
rs754280878 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475412 | AGGCAGGGAAGGTGA[A/G]GCTTTAGTGAGCCAA | 89910 |
rs754281028 | snp | C/T | 1.80873e-05 | 0.00300721 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534785 | TGAACTCTCCTAGCT[C/T]CTGTCCCAGCCCTGC | 89910 |
rs754321780 | snp | C/T | 1.64727e-05 | 0.00286986 | stop-gained, intron-variant | UBE3B | GRCh38.p7 | 12:109529999 | AAACCCGAGTGGATC[C/T]GAATGTTCTCAACTC | 89910 |
rs754324814 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541962 | TTACCTTAATTACAT[C/T]TACAAAGACCTGTTT | 89910 |
rs754341321 | snp | C/T | 1.64895e-05 | 0.00287132 | intron-variant | UBE3B | GRCh38.p7 | 12:109490013 | GCTGCAGGTCTGTGA[C/T]TCCTGCCCCCCAGTG | 89910 |
rs754354555 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502178 | CTGTGAACCAACATG[A/C]AATGTTTCAGAAACC | 89910 |
rs754368148 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500654 | GAGAGCAGCACCTCC[A/G]CAGACAGCCTGCTCT | 89910 |
rs754392434 | in-del | -/TCT | 0.00010621 | 0.00728653 | intron-variant | UBE3B | GRCh38.p7 | 12:109499858 | GCCTCTCTCCCACCA[-/TCT]TCTTCTTCCTTCTTT | 89910 |
rs754416261 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516832 | TGGTGGAAACCAGCT[C/T]TGCCTCCCCGCATGT | 89910 |
rs754419254 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488916 | TTCTTCTGATTTTAA[C/T]TTTTATAGTTCCCAC | 89910 |
rs754511954 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538756 | GCACTTAGGCAAGAT[C/T]GGAGGAAAGTCACAT | 89910 |
rs754514239 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530024 | CAACTCCTGAACTGC[A/C]GCGTCTCATCTCTGG | 89910 |
rs754568858 | snp | A/G | 1.65452e-05 | 0.00287616 | intron-variant | UBE3B | GRCh38.p7 | 12:109530092 | GAGGCGGGTGGGGGG[A/G]AGGGTGAAATTCCTT | 89910 |
rs754594106 | snp | A/G | 3.29554e-05 | 0.00405914 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501401 | GCACTTGATCACCAA[A/G]CAGCTGCAGTTCTTG | 89910 |
rs754612044 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486166 | TTAGGACCAATTCAC[A/G]CACAAATGCAAATAA | 89910 |
rs754690536 | snp | C/T | 3.29853e-05 | 0.00406098 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491121 | CAGCTTTTTCTCTAG[C/T]GTTACGGTGAGTAAG | 89910 |
rs754724440 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517646 | TCCTGCCAGCGATAG[A/G]ATTGGTGACTGAGCC | 89910 |
rs754781555 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505076 | GCTCACATTGAAGCT[A/C]ATTTTCCCAAGTGAG | 89910 |
rs754811157 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529792 | TTTGTGTTTTTTGTA[A/G]AATGGTTCAGAAATG | 89910 |
rs754846113 | snp | A/G | 1.65759e-05 | 0.00287883 | intron-variant | UBE3B | GRCh38.p7 | 12:109523951 | GAATCCTGGCTGATG[A/G]ACAGCTCTGCTTCTC | 89910 |
rs754848171 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518459 | CACCAAATTCAACCT[G/T]TGGGCCACCCATTTG | 89910 |
rs754858689 | snp | C/T | 1.66076e-05 | 0.00288158 | intron-variant | UBE3B | GRCh38.p7 | 12:109498188 | ACTCTCTACAGGAAA[C/T]TGTTTCTGGCAGTTT | 89910 |
rs754874975 | snp | G/T | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535335 | CCCATCTGCTGCCCA[G/T]GGAAGCGCAGGCGCC | 89910 |
rs754877736 | snp | A/G | 4.18857e-05 | 0.00457614 | intron-variant | UBE3B | GRCh38.p7 | 12:109510510 | AGCCTGCTCCGGCAC[A/G]CTGCCCGAGCACTCA | 89910 |
rs754879316 | snp | A/C | 2.04887e-05 | 0.00320061 | intron-variant | UBE3B | GRCh38.p7 | 12:109486586 | TCAAGGTAACAAAAA[A/C]AAAAAAAAAAAAAAA | 89910 |
rs754894664 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507793 | GGAGAGACCAAAATA[C/G]AGTGTCAGTAAGGAA | 89910 |
rs754907304 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506273 | CAGACTACTGTTGGG[G/T]GGCCAAATCCAGCCC | 89910 |
rs755050744 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524950 | CGCAGCACGTCTCCT[A/C]CCACGGTTCCTTCTG | 89910 |
rs755054789 | snp | C/G | 3.29527e-05 | 0.00405898 | intron-variant | UBE3B | GRCh38.p7 | 12:109526341 | TCCCTATTAATTACT[C/G]CCATCTTCTCCCCCA | 89910 |
rs755094094 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524567 | CCTGAGACCTGCCGT[A/G]TTATTTGTTTTCCTC | 89910 |
rs755102431 | snp | C/T | 0.000320273 | 0.0126505 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534575 | CCCAATTCAAGGCCA[C/T]GATGTGTGCCTTCAG | 89910 |
rs755107792 | snp | C/G | 1.85197e-05 | 0.00304295 | intron-variant | UBE3B | GRCh38.p7 | 12:109511350 | GTCTTTCTATTCCCC[C/G]ACGTGGTTCCTGCCT | 89910 |
rs755119744 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494939 | CCTTTGTACCCTTAT[A/G]ACAATGCAGTCCTTT | 89910 |
rs755172467 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483106 | CTTGGCAAAATAAAA[A/G]CTGACCTCTCAGTTT | 89910 |
rs755173837 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant | UBE3B | GRCh38.p7 | 12:109489878 | AAACAGGTCACATTA[C/T]GGCAAGAGACTTTTT | 89910 |
rs755200485 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512220 | AGTCAGGGAATCAGA[C/T]AGCACCCAAGTCTGC | 89910 |
rs755281867 | snp | A/G | 1.71346e-05 | 0.00292694 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477310 | CGGACTGAGAGAGGC[A/G]GGAAACACCCAGCTC | 89910 |
rs755325921 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541084 | GCTCCTGGGGCCTCT[A/G]GCCAAACCACTGCTG | 89910 |
rs755351128 | snp | A/C | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507715 | GATGCTGTTCTGTGA[A/C]TGTTCGCGGCACCTC | 89910 |
rs755365552 | snp | G/T | 3.3006e-05 | 0.00406226 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483923 | AAAGAAGTGCACTTT[G/T]TATTTTCAAGATTGC | 89910 |
rs755377279 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531479 | TTTTGCCATGTTCTG[C/G]TGGTAAATTTAGTGC | 89910 |
rs755391870 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520481 | ACCACCAGCCAGAAG[C/T]CCAGGCCCAGCACCA | 89910 |
rs755402322 | snp | A/G | 4.94254e-05 | 0.00497094 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498306 | ACCAAGATCGATGCC[A/G]TGATGTATGTGAAAG | 89910 |
rs755472931 | snp | A/G | 1.72252e-05 | 0.00293467 | intron-variant | UBE3B | GRCh38.p7 | 12:109509563 | TCGCCTTTTTTCAGT[A/G]TGGAATTGTGGGTAA | 89910 |
rs755484440 | snp | A/G | 0.000185443 | 0.00962741 | intron-variant, synonymous-codon | UBE3B | GRCh38.p7 | 12:109533983 | CTGCTTCATTTCCTC[A/G]TTGGCCAAAGGAGAA | 89910 |
rs755570182 | snp | A/G | 0.000132492 | 0.00813809 | intron-variant | UBE3B | GRCh38.p7 | 12:109530101 | GGGGGGAAGGGTGAA[A/G]TTCCTTGGCCTCCCA | 89910 |
rs755585889 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479691 | AAGGATGAGAAAAAC[G/T]GTAAAGTGTAGGCTA | 89910 |
rs755644890 | snp | A/G/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521193 | CAGCACGCCATGAAG[A/G/T]GGGTCATCCGTGTGA | 89910 |
rs755667791 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538557 | GACGCACCCAGCGCA[A/G]CACCTGGCACCAAGT | 89910 |
rs755684157 | snp | C/G | 0.000204859 | 0.0101187 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509744 | GTCTGCTGTTGTTTG[C/G]TTGATGCTGCACCCA | 89910 |
rs755700009 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508737 | AAGCCAAGAGTGAAT[C/T]TTATTCTAGTGTATG | 89910 |
rs755711617 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517009 | TGAAATTAAGGCTCT[C/G]GGAGCAGGAAAGGGG | 89910 |
rs755741894 | snp | C/T | 1.65094e-05 | 0.00287305 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491143 | GTGAGTAAGAAACCA[C/T]AGCTGAGGTGTTGGC | 89910 |
rs755781431 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512414 | TTGGGGAGGATTGGG[C/T]TGTGGCAGGAGCATC | 89910 |
rs755789202 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496105 | CTGGCAACAACTAAT[C/G]TACTTTCTATCTCTT | 89910 |
rs755799083 | snp | A/T | 1.65627e-05 | 0.00287769 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483965 | TGTTCCTATTCAGAA[A/T]CAAAGAGGATAATGA | 89910 |
rs755845246 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497144 | AATACATGCTTATTG[C/T]AGAAAACCTAGATAA | 89910 |
rs755856794 | snp | C/T | 8.34272e-05 | 0.00645807 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486067 | ATGCTGAGAATGAGC[C/T]TAAGGTAAGTGGACG | 89910 |
rs755858165 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527425 | AACTGTTAATTGGAG[C/T]ATCAGTCTCTTTAGT | 89910 |
rs755911353 | in-del | -/TGTT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505264 | AACTTAGGAAGTGTC[-/TGTT]TGTGCTCCTCACACA | 89910 |
rs755913033 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482587 | GGATTTCTGAATAAT[-/A]TCATTTCAGTGTTTT | 89910 |
rs755935755 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539149 | GCTGAGGCTGGAGAA[C/T]TGCTTGAACCCAGGA | 89910 |
rs755976350 | snp | C/T | 3.80272e-05 | 0.00436029 | intron-variant | UBE3B | GRCh38.p7 | 12:109511178 | CCTTCTTTTAATTCT[C/T]CCAAACCCATGTCTT | 89910 |
rs755988562 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528462 | GATATTTTTGAGATT[A/G]CTAAAGCTTTAGCAT | 89910 |
rs756006509 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517563 | CTTAACTACCTACGA[C/T]GTCTGTGTTATCCAT | 89910 |
rs756009671 | snp | C/T | 0.000200558 | 0.0100119 | intron-variant | UBE3B | GRCh38.p7 | 12:109501540 | CCAGTGAAGAGTGAG[C/T]GACGGGAGCAGGCCC | 89910 |
rs756015112 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109543509 | CACCCTACCTGGAAT[C/T]GATCCTTTGTTTCTC | 89910 |
rs756049801 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504906 | CGCCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT | 89910 |
rs756125877 | snp | C/T | 1.64939e-05 | 0.0028717 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491056 | TCAGATATTGTTAAC[C/T]CGTGGCCTGGCAAGA | 89910 |
rs756208404 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109492312 | ATTTCAAATGCTCAG[C/T]GGCCACATGTAACTA | 89910 |
rs756221182 | in-del | -/TGTTTTTCTTTTC | 1.64988e-05 | 0.00287213 | intron-variant | UBE3B | GRCh38.p7 | 12:109497963 | GTGAAAACCCAATTG[-/TGTTTTTCTTTTC]TTCTTAAACATTAGA | 89910 |
rs756245634 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506048 | ATGTGGCCTGTGTGT[C/T]TAAGGCCTTGTAGCC | 89910 |
rs756250265 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533837 | ACGTGCTGTTTTTAG[C/T]GGCGTCTGGCCTCAC | 89910 |
rs756261850 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481227 | GAGGCTGAAGCAGGA[A/G]AATCGCTTGAACCTG | 89910 |
rs756262426 | snp | A/C | 1.65831e-05 | 0.00287945 | intron-variant | UBE3B | GRCh38.p7 | 12:109516714 | AGAGTGTTTTTATGG[A/C]ATCGTCAGTTTGCTG | 89910 |
rs756267187 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503062 | AGTCGGCATCAGTCC[A/G]GAATATTCTCAGGCC | 89910 |
rs756278716 | in-del | -/TTT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520744 | GTTCTGTAGGTTTGA[-/TTT]TTTTTTTTTTTCTTT | 89910 |
rs756283868 | snp | A/G | 1.7703e-05 | 0.0029751 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483558 | TTTGCAAACATGTTC[A/G]CCCTGTCTCAGACCT | 89910 |
rs756305761 | snp | C/T | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535197 | ACAAAGCCTACTGTG[C/T]GTGAGATCCTCTCCT | 89910 |
rs756382904 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500339 | GAATTTGAAATATCT[A/C]CCTGAGCTGAGATAA | 89910 |
rs756415175 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536991 | TGGGTGTATATCTTT[A/G]CAGTCCATGTTTTAC | 89910 |
rs756453947 | snp | C/T | 8.65928e-05 | 0.00657943 | synonymous-codon, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534593 | TGTGTGCCTTCAGGA[C/T]ACCGGGGACACTCTG | 89910 |
rs756494569 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512080 | GTTCAGCATCGAGCA[A/G]GTAGGATGTGAGATG | 89910 |
rs756503210 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540385 | GCTAGTTTATTTTGT[A/G]TTTTTTATAGAAACA | 89910 |
rs756503841 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542956 | CACATGTTTGGAAGA[A/G]GTCAAACCAGGATTT | 89910 |
rs756517854 | snp | A/T | 5.79391e-05 | 0.00538203 | intron-variant | UBE3B | GRCh38.p7 | 12:109510295 | CTGTCCTCCCCTTGC[A/T]CTCTGGCTCTGACTC | 89910 |
rs756519602 | snp | C/G | 2.03407e-05 | 0.00318903 | intron-variant | UBE3B | GRCh38.p7 | 12:109499629 | CAGCCTTCTCTCTCT[C/G]TAGGCAACCTCCTAC | 89910 |
rs756539409 | snp | A/C/G | 3.29616e-05 | 0.00405954 | intron-variant | UBE3B | GRCh38.p7 | 12:109489885 | TCACATTATGGCAAG[A/C/G]GACTTTTTTGTTCTC | 89910 |
rs756556511 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541047 | CTCTGAGTCCACCAT[C/T]CTTGCAGCTATGCAG | 89910 |
rs756634268 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488113 | GAAAGCAGTGTTACT[A/G]TTTCTGGTCAACAGA | 89910 |
rs756634558 | snp | C/G | 1.64754e-05 | 0.00287009 | intron-variant | UBE3B | GRCh38.p7 | 12:109526355 | TCCCATCTTCTCCCC[C/G]AGCTTGTTTGCCATG | 89910 |
rs756691692 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501846 | TTTTTTAATTTTTGT[A/G]GAGATGGGGGCCTTA | 89910 |
rs756704788 | snp | A/G | 1.65091e-05 | 0.00287303 | intron-variant | UBE3B | GRCh38.p7 | 12:109521352 | AGCAACAGCAGGGCT[A/G]ACAGCAGCCAGATTC | 89910 |
rs756750354 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512177 | GAGCACCCAAATCTC[C/T]TGACTGCCCCCATGG | 89910 |
rs756757808 | snp | C/T | 3.30235e-05 | 0.00406333 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509659 | GGAAGAGCTGGTCAC[C/T]ATCTCCTCTTTCCTG | 89910 |
rs756812580 | snp | A/G | 1.64904e-05 | 0.00287139 | intron-variant | UBE3B | GRCh38.p7 | 12:109533428 | CCTGGAAGAGCAGGA[A/G]CCTGCCCCGTCCCCA | 89910 |
rs756821406 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109521008 | AAGCAGGTGAGAACG[A/G]CTCCTGTCATGCATC | 89910 |
rs756839984 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510664 | CACCAAATATGATTA[A/G]AGTTAATTAATGGCA | 89910 |
rs756842533 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520341 | AAGGCCTCAACAGAT[C/T]AGAATCAAGAGACAA | 89910 |
rs756867523 | snp | A/G | 1.72291e-05 | 0.002935 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521484 | CCTCACCCACATCCT[A/G]CATCCATGAGAATTA | 89910 |
rs756881415 | snp | C/T | 4.88293e-05 | 0.00494088 | intron-variant | UBE3B | GRCh38.p7 | 12:109510330 | TCTGACTTTCCTGTT[C/T]GTTTGTCCCACAGAG | 89910 |
rs756908037 | snp | A/G | 1.65239e-05 | 0.00287431 | intron-variant | UBE3B | GRCh38.p7 | 12:109486467 | CTCTTTTTCCCACCT[A/G]TAGGTGTGGTATGTG | 89910 |
rs756928925 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507406 | TATCATTGTTACTCT[C/T]GTGGTGATAATGCTT | 89910 |
rs756974730 | in-del | -/TT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520745 | TTCTGTAGGTTTGAT[-/TT]TTTTTTTTTTTCTTT | 89910 |
rs756982317 | snp | A/G | | | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508555 | GAATTATAAGATACA[A/G]TGGACCTCAGGCAGT | 89910 |
rs756990736 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537446 | CCTGGCCTGGGAAGC[C/T]CCTGAGGATCAGAGC | 89910 |
rs757006162 | snp | A/T | 1.68986e-05 | 0.00290672 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477240 | CTCAACCCCTAGTCC[A/T]TGGGCACCGCCCTCC | 89910 |
rs757068440 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525945 | TCCAGAAATGATGCC[A/G]TTCTGTGCATGTTGT | 89910 |
rs757087258 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525995 | CACCTTTTTAGTAAA[C/T]GCACATTTTCATCAT | 89910 |
rs757091450 | snp | C/T | 1.80331e-05 | 0.00300271 | intron-variant | UBE3B | GRCh38.p7 | 12:109511345 | GATGTGTCTTTCTAT[C/T]CCCCCACGTGGTTCC | 89910 |
rs757142758 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503027 | CTCCATGCCAGGTCT[C/T]CTAAAGCGTGCTTTT | 89910 |
rs757150512 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497827 | GTCTAGCCCTGTGAT[C/T]GCTGCACAGTTCTCA | 89910 |
rs757183837 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495879 | TCCAGTAGACCTACA[A/C]CCTTCTGGCCGTGGG | 89910 |
rs757192855 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484462 | GTGGCGCAGTCTTGG[C/G]TCACTGCCAGTCTTC | 89910 |
rs757330991 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480623 | ACCACTGCACTCCAG[C/T]TTGGATGACAGAGCG | 89910 |
rs757335488 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502636 | GGTTGTCACGCCTTA[C/T]TTCCCTCTAAAGGCA | 89910 |
rs757386264 | snp | A/G | | | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490845 | TTTTTTAAGAGACAG[A/G]GTTGCCCTGTCACCC | 89910 |
rs757388043 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542268 | ACTGTGTCTTCATGT[C/G]CTGCTTTCAGCAGTC | 89910 |
rs757404245 | snp | C/G | 1.66788e-05 | 0.00288775 | intron-variant | UBE3B | GRCh38.p7 | 12:109516902 | GAGTGTGAAGCCTAT[C/G]GAATCCTACCACAAG | 89910 |
rs757416018 | snp | A/G | 1.65586e-05 | 0.00287733 | intron-variant | UBE3B | GRCh38.p7 | 12:109523955 | CCTGGCTGATGGACA[A/G]CTCTGCTTCTCTGCT | 89910 |
rs757437325 | snp | A/C | 1.65111e-05 | 0.0028732 | intron-variant | UBE3B | GRCh38.p7 | 12:109486605 | AAAAAAAAAAAAAAG[A/C]AAAACCAGAAACAGT | 89910 |
rs757444304 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533729 | GCAGGAGAACCAGCC[A/G]GCCCCAGAGAGACTG | 89910 |
rs757445125 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109543394 | CGGCTGGTAACACAG[C/G]AGGACTCGGCTGAGG | 89910 |
rs757449649 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507186 | ATTTAAAGCATAAAT[G/T]CTAAGTCAGACCTGA | 89910 |
rs757461338 | snp | C/T | 0.000103641 | 0.00719791 | intron-variant | UBE3B | GRCh38.p7 | 12:109507528 | GACCAGGTGGAGTCT[C/T]CACCTGAAGCTTGGG | 89910 |
rs757468470 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504868 | GTAGTGCAGTAGCGC[A/G]ATCTCGGCTCAACTG | 89910 |
rs757511606 | snp | C/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498292 | CATATTTTTAAGAGA[C/G]CAAGATCGATGCCGT | 89910 |
rs757520929 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109492183 | GCCATAGTTTATAAA[C/T]ACCTGGTCTAGACTG | 89910 |
rs757534213 | snp | C/T | 1.68354e-05 | 0.00290128 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534674 | CCGCCTGCCCACCTC[C/T]TCCACCTGCTTCAAC | 89910 |
rs757591265 | snp | A/G | 8.24804e-05 | 0.00642132 | intron-variant | UBE3B | GRCh38.p7 | 12:109529879 | TGTTATCTCTTCCTT[A/G]TTGGCAACAGAATTA | 89910 |
rs757616037 | snp | C/T | 1.76372e-05 | 0.00296956 | intron-variant | UBE3B | GRCh38.p7 | 12:109499853 | TTCCTGCCTCTCTCC[C/T]ACCATCTTCTTCTTC | 89910 |
rs757663823 | snp | A/C | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510111 | TAGACTTAAAAGGCC[A/C]TTCGGATGACACACT | 89910 |
rs757668753 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510831 | GTTTTTTGGAGAGTA[A/G]TGGGGTGGGGGAAAT | 89910 |
rs757679020 | snp | A/G | 3.44323e-05 | 0.00414909 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483575 | CCTGTCTCAGACCTC[A/G]AGAGCATGGTTCATC | 89910 |
rs757680127 | snp | A/C/T | 0.000164952 | 0.00908024 | intron-variant | UBE3B | GRCh38.p7 | 12:109490019 | GGTCTGTGACTCCTG[A/C/T]CCCCCAGTGTGCAAC | 89910 |
rs757722460 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530000 | AACCCGAGTGGATCC[A/G]AATGTTCTCAACTCC | 89910 |
rs757731326 | in-del | -/T | 1.78662e-05 | 0.00298878 | intron-variant | UBE3B | GRCh38.p7 | 12:109499860 | CTCTCTCCCACCATC[-/T]TCTTCTTCCTTCTTT | 89910 |
rs757776936 | snp | C/T | 4.94564e-05 | 0.0049725 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516835 | TGGAAACCAGCTCTG[C/T]CTCCCCGCATGTCAC | 89910 |
rs757786448 | snp | C/T | 3.34975e-05 | 0.00409238 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483672 | ATCCAGGCCCATGTC[C/T]GGAGTTTTCTCTGTC | 89910 |
rs757814302 | snp | A/G | 3.59228e-05 | 0.00423793 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534764 | CATCAGCATGAACAC[A/G]GGCTTTGAACTCTCC | 89910 |
rs757818603 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109521824 | AGGAGTCACCTGTCC[A/C]GAGTTTCGTTGCTAG | 89910 |
rs757898120 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499746 | AAGTATGTGTCTCAG[A/G]AGAAGTCCAACCTGA | 89910 |
rs757904528 | snp | C/T | | | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508596 | CTGGAAGACTTTAGC[C/T]GGAGAGGATCAGGGA | 89910 |
rs757910834 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540309 | GCCTCCGAGGCTCAA[C/G]CAATCCTCCCACCTC | 89910 |
rs757937564 | snp | C/T | 1.7232e-05 | 0.00293525 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534722 | CTACAGCAAGAAGAG[C/T]GTCCTCCGCGAGAAG | 89910 |
rs757940998 | in-del | -/TCTC | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484419 | TTTTTTGAGATGAAG[-/TCTC]TCTCTGTCGCCAGGC | 89910 |
rs757964808 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528943 | ACGGGCAGATCACCC[A/G]AGGTCAGGAGTTTGA | 89910 |
rs757976738 | snp | A/C/G | 3.29496e-05 | 0.00405881 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109529922 | TGATGGCACATTTTC[A/C/G]AATGCACACTCAAAT | 89910 |
rs757995890 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506574 | CAGGCTGGTCTCAAA[C/G]TCCTGACCTCAGATG | 89910 |
rs758014451 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476530 | CTTGAAACATCCTCC[G/T]CTCCTTAGGCGTGGT | 89910 |
rs758033351 | snp | C/G | 1.65214e-05 | 0.0028741 | intron-variant | UBE3B | GRCh38.p7 | 12:109501323 | GGGCTGGCCCTGGCC[C/G]TGCATCAGATGGAAC | 89910 |
rs758034388 | snp | C/T | 0.0001638 | 0.00904838 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510427 | CGGGACTGCCGGCGG[C/T]GCTTCACCCCCGAGG | 89910 |
rs758071173 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518547 | GCACTTCCCTCTGCA[G/T]ACCCAGATGCATCTC | 89910 |
rs758080209 | snp | C/T | 2.07613e-05 | 0.00322184 | intron-variant | UBE3B | GRCh38.p7 | 12:109490080 | TTTTACATTTGCATT[C/T]AGCATACCTGGTGTC | 89910 |
rs758113064 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494901 | CATAGGTTTCTGTGA[A/G]AACCCCTAGAGAATG | 89910 |
rs758132473 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520058 | AGCCTGTCTAACCTG[C/T]GAAGCATGTGACAGT | 89910 |
rs758212453 | snp | A/G | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533515 | GATTCGCCTACCTCA[A/G]GCCTCCATTCTCCAT | 89910 |
rs758243999 | snp | C/T | 8.24382e-05 | 0.00641968 | intron-variant | UBE3B | GRCh38.p7 | 12:109533436 | AGCAGGAGCCTGCCC[C/T]GTCCCCACTGACCCT | 89910 |
rs758248355 | snp | A/G | 9.88419e-05 | 0.00702931 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503150 | CCTCTACCAGACCTC[A/G]CTGACAACTCTCACA | 89910 |
rs758250458 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497835 | CTGTGATTGCTGCAC[A/G]GTTCTCAGACAATCT | 89910 |
rs758267073 | in-del | -/CT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541578 | TGGGTCAGAAGGTAA[-/CT]CTCATTGCTGTTCTA | 89910 |
rs758268257 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507274 | TTCTGTGCTTCAGTT[A/T]CCTCCTGTATAAGAT | 89910 |
rs758272839 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537295 | CACAGGACACGCAGC[C/T]GTTCTCACTGCATTC | 89910 |
rs758290112 | snp | C/T | 3.30028e-05 | 0.00406205 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486477 | CACCTATAGGTGTGG[C/T]ATGTGTCCCTGGCTT | 89910 |
rs758301802 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497898 | TGCCTGCTCTGGTGA[C/T]TCATCTCAGCACAGT | 89910 |
rs758321616 | snp | A/T | 8.27164e-05 | 0.0064305 | intron-variant | UBE3B | GRCh38.p7 | 12:109486122 | TCTTAAGGGCCAACC[A/T]ACTGGGCTCTGAAAG | 89910 |
rs758321665 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495094 | TTCTCTTTTCATGTG[A/C]CCCACTCAGATCAGA | 89910 |
rs758351341 | snp | C/G | 1.71711e-05 | 0.00293006 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521504 | CATGAGAATTACCTG[C/G]AGCTCTTCGAGTTTG | 89910 |
rs758352712 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483243 | ATTCTTTGTTCATTC[A/G]TAAAGCTGGGCCTGC | 89910 |
rs758425773 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541138 | GTGGTCCACCTGCCT[A/G]CGGCTGAGTGGCCTT | 89910 |
rs758431867 | snp | C/T | 0.000192845 | 0.00981761 | intron-variant | UBE3B | GRCh38.p7 | 12:109533877 | AGATCTGAGGCAGCA[C/T]GGGAGAAAGTGAGAG | 89910 |
rs758454164 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513783 | AGGAAAATGGGGCCC[G/T]CGTCATCTCCTGCCC | 89910 |
rs758475447 | snp | C/T | 1.68587e-05 | 0.00290329 | intron-variant | UBE3B | GRCh38.p7 | 12:109533679 | GGCAGCTGGACCCCT[C/T]AGAGCCAAGTGAGGA | 89910 |
rs758489290 | snp | A/G | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524451 | AGCGCTATGATGGGG[A/G]CATCACTGACCTGGG | 89910 |
rs758536392 | snp | C/T | 3.29544e-05 | 0.00405908 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524085 | GCCTTCTCTGGACTC[C/T]GAGTTCTATAAAAAC | 89910 |
rs758612295 | snp | C/T | 1.64751e-05 | 0.00287007 | stop-gained, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498299 | TTAAGAGACCAAGAT[C/T]GATGCCGTGATGTAT | 89910 |
rs758631445 | in-del | -/AT | 1.65055e-05 | 0.00287271 | intron-variant | UBE3B | GRCh38.p7 | 12:109503000 | TGAGCTGCTGCTCAC[-/AT]GTCTTCTTTTCTCCA | 89910 |
rs758659249 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488603 | ACTCCCGACTCATCA[A/C]CCTGTACCTCACGAT | 89910 |
rs758676781 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493000 | CCATATTAGACCACA[A/T]GCCTCTAGAGGCTAG | 89910 |
rs758710259 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489256 | ATTAAATAGATGTCG[C/T]TCATAGATATAAAAT | 89910 |
rs758725785 | snp | C/T | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533532 | CCTCCATTCTCCATC[C/T]GCTGCGTGGAGGTGT | 89910 |
rs758727981 | snp | A/C | 1.67181e-05 | 0.00289115 | intron-variant | UBE3B | GRCh38.p7 | 12:109516912 | CCTATGGAATCCTAC[A/C]ACAAGGAAGTGGGCC | 89910 |
rs758748721 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109530007 | GTGGATCCGAATGTT[C/T]TCAACTCCTGAACTG | 89910 |
rs758754192 | snp | C/G | 3.3493e-05 | 0.00409211 | intron-variant, missense, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491019 | AGTTGATATCATCCT[C/G]TGACCAATTAAAACA | 89910 |
rs758799716 | snp | A/G | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521444 | TTTGCCTTGCAGACA[A/G]CCAGTGGGGATGAGA | 89910 |
rs758807549 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479795 | AATTTCTTATTCTGG[A/G]AGGGCCCCTGGGAGA | 89910 |
rs758821239 | in-del | -/TT | 1.64741e-05 | 0.00286998 | frameshift-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521296 | AGATCATCAAGAGAG[-/TT]TTTGACCCAGCACTC | 89910 |
rs758851018 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522703 | TCTGGAAACAGTCTA[C/T]GTGCACCGGCCTCAG | 89910 |
rs758877442 | snp | G/T | 1.7184e-05 | 0.00293117 | intron-variant | UBE3B | GRCh38.p7 | 12:109483745 | CCTAGCACATGATTC[G/T]CTGGCTCCCAATTAA | 89910 |
rs758912603 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481779 | GCTGGGGCAGGAAGC[A/G]TAAATGATTCAGAAG | 89910 |
rs758966447 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494400 | CATTGATTTTCTGGA[C/T]GCCTAGTTTGCCCAG | 89910 |
rs758974816 | snp | A/C | 1.65312e-05 | 0.00287495 | intron-variant | UBE3B | GRCh38.p7 | 12:109498217 | TTCTGATTTAACGGT[A/C]TGCTATTCTTTGCAG | 89910 |
rs759054166 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520923 | CCCCTTGAGGTCAGT[C/G]TCCCCTTGCCAAGGA | 89910 |
rs759145811 | snp | C/T | 3.30224e-05 | 0.00406326 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511253 | GACAGGGACAGAAAA[C/T]GGGCACAGTTGATCC | 89910 |
rs759184843 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500263 | AAAGTGTAATTATGA[A/G]CTTAAAAACATGAGA | 89910 |
rs759206834 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539914 | CTTTTCTTACCGTGA[C/T]AGTCCAAGTGTTTTC | 89910 |
rs759212606 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512688 | CTCACTGCTGTCTGA[C/T]ACTGTTCTGTCCTTG | 89910 |
rs759231007 | snp | A/G | 1.69761e-05 | 0.00291337 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477278 | GAAAAGTCGGAGGAC[A/G]CAGGAGTCTCCAAAC | 89910 |
rs759233802 | snp | A/G | 1.65433e-05 | 0.002876 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501514 | AGCCAGCATCCCCTC[A/G]GAATGTGCTCCCAGT | 89910 |
rs759244593 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109499081 | ACACGCCTCAGCCTG[C/T]GAGATTACAGACTTG | 89910 |
rs759246438 | snp | C/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536284 | TGGACTTGCCACTTT[C/G]TCCAAACGCTCGGTT | 89910 |
rs759254157 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482746 | TAGGAAAAAACAGTT[A/G]CTGGTGATTTAGATA | 89910 |
rs759305768 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487864 | TGAGCTTTGAGGTTT[C/G]AACTCAGTGGTCTCC | 89910 |
rs759347259 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519719 | GCTGCCTGTTGACTT[C/T]CTGTTTCTCCCTTTT | 89910 |
rs759383140 | in-del | -/TTC | 1.74442e-05 | 0.00295327 | intron-variant | UBE3B | GRCh38.p7 | 12:109511192 | CCCAAACCCATGTCT[-/TTC]TTCTTCTCAAGGGAT | 89910 |
rs759401110 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540906 | CAGGTGGTGAGGAGG[C/T]ATGAGAGCGGCTCTG | 89910 |
rs759408557 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507112 | AGAGACCTTCTGGCC[C/G]ACAGTGCCTAAAAAT | 89910 |
rs759425173 | snp | C/G | 0.000175147 | 0.00935642 | intron-variant | UBE3B | GRCh38.p7 | 12:109533775 | CTCTCTCGGCAGCCC[C/G]TTTCTCTTTCCTTCC | 89910 |
rs759450133 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109530900 | CCTGCACAGGTGGGC[A/C]TACCTGTTGTGCTCG | 89910 |
rs759461082 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534481 | GCCCTGCACTCTGCC[C/T]AGCATCCAGGGACTG | 89910 |
rs759485665 | snp | C/T | 1.67528e-05 | 0.00289415 | intron-variant | UBE3B | GRCh38.p7 | 12:109507757 | TGACTGCTGTGGGAC[C/T]GAATTCCTTTCCTAG | 89910 |
rs759503614 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532026 | AGTGGATGTGACCAC[C/G]ACCATGCTTCTCTTA | 89910 |
rs759528348 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520671 | ACTTGCAGGCACTTC[A/G]TGATTGGGAAGGCAG | 89910 |
rs759572123 | in-del | -/ATTAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529528 | GTCCAGAAGAATGAG[-/ATTAA]ATGAAAGTCCAAAAA | 89910 |
rs759607042 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529076 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGT | 89910 |
rs759613604 | in-del | -/TGCCCC | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517929 | GAGAGCTTGTTTGAG[-/TGCCCC]TGGCCACTGGTGATC | 89910 |
rs759709669 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488395 | CTAGAGTGCCACATT[-/C]CCTGTTATTTAACTC | 89910 |
rs759732375 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508124 | ACCCTGGGCAAGGGA[A/T]CACGGATTCAACCTC | 89910 |
rs759737421 | snp | G/T | 1.68633e-05 | 0.00290368 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534654 | CGCAAGCGGGAGCCA[G/T]GCGGCCGCCTGCCCA | 89910 |
rs759741155 | in-del | -/TT | 6.57613e-05 | 0.00573379 | intron-variant | UBE3B | GRCh38.p7 | 12:109490110 | CCTCCTCAGAAACAC[-/TT]TTCATAGGAAGAGCT | 89910 |
rs759754597 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525781 | AATATGAGCAAAAGA[C/T]GAAAAGATAATGAAA | 89910 |
rs759764206 | in-del | -/AA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481313 | GAGTGAGACTATCTC[-/AA]AAAAAAAAAAAAAAG | 89910 |
rs759771388 | snp | A/G | 1.71393e-05 | 0.00292734 | intron-variant | UBE3B | GRCh38.p7 | 12:109499822 | ATGGGTGAGTCCCAG[A/G]TGCAAATCACTGTCT | 89910 |
rs759782924 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496427 | TCCCTGGGTCATGTG[A/G]TAACTCCATGCTTAA | 89910 |
rs759783015 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484224 | GAGTCAGGAAGTTTA[A/G]GTAAATGAGTAAAAA | 89910 |
rs759788668 | snp | C/G | 1.75696e-05 | 0.00296386 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534738 | GTCCTCCGCGAGAAG[C/G]TGCGCTACGCCATCA | 89910 |
rs759813881 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516787 | TACTGTTTCGAACCA[C/T]GGTTACCAAGGAGAA | 89910 |
rs759816886 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530564 | AGCACACAGTCTACT[A/G]CGGTGGTTTCCATGG | 89910 |
rs759826641 | snp | C/G | 3.30458e-05 | 0.0040647 | intron-variant | UBE3B | GRCh38.p7 | 12:109490028 | CTCCTGCCCCCCAGT[C/G]TGCAACTTCTCCACT | 89910 |
rs759845242 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109529966 | GCTGCCCTCATTAGC[A/G]GATTCCGTTCCATTA | 89910 |
rs759870756 | in-del | -/CAAGG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538213 | GAGCCTGTTAGCAGA[-/CAAGG]CACTGCTGAAAGCCA | 89910 |
rs759887413 | in-del | -/TTTTTTTTT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516167 | TTTTTCTTTTTTTTC[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 89910 |
rs759890228 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487524 | GAGACATGGCTCAGC[A/G]CAGGGTTTCCACACT | 89910 |
rs759946467 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521314 | TTGACCCAGCACTCA[A/G]TCTGTTCAAGGTATT | 89910 |
rs759949448 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540410 | GAAACAGGGTTTTGC[A/C]ATATTGCCCACGCTG | 89910 |
rs759953360 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479523 | GAACCAAGGCCCGCT[C/T]TCTCTGATGCAAGAC | 89910 |
rs759993199 | snp | C/T | 3.33739e-05 | 0.00408483 | intron-variant | UBE3B | GRCh38.p7 | 12:109486442 | ATCTCTATAACAGCC[C/T]ATGACATTCCTCTTT | 89910 |
rs759997769 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527684 | TTAGAAGGAACAAAG[-/T]GCAGATTGGGAGGGA | 89910 |
rs759998061 | snp | A/G | 1.65581e-05 | 0.00287728 | intron-variant | UBE3B | GRCh38.p7 | 12:109530679 | TTATTTATTACCTAT[A/G]CATGCATGCATGTAT | 89910 |
rs759999382 | snp | A/G | 1.73905e-05 | 0.00294872 | intron-variant | UBE3B | GRCh38.p7 | 12:109521432 | TCTCCCCGTCTTTTT[A/G]CCTTGCAGACAACCA | 89910 |
rs760000328 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527773 | GCCCCTGCCTGCCAT[A/G]TAACCTGTAGCCATT | 89910 |
rs760038282 | snp | C/G | 1.72597e-05 | 0.00293761 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521531 | TTTGTGGGGAAGATG[C/G]TGGGGAAGGCTGTGT | 89910 |
rs760039819 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491642 | CACCTGCAATTCTGA[G/T]AATTGCCAAATGTAA | 89910 |
rs760040837 | in-del | -/TT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515360 | TACTATTATTACTGT[-/TT]TTTTTTGTTGTTGTT | 89910 |
rs760043580 | snp | A/G | 1.64857e-05 | 0.00287099 | intron-variant | UBE3B | GRCh38.p7 | 12:109497783 | CTGGATGCACACGGA[A/G]ACCTGTCTGAATGAG | 89910 |
rs760050754 | snp | A/C | 1.72531e-05 | 0.00293705 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509756 | TTGGTTGATGCTGCA[A/C]CCAGGGAGGCCGAAG | 89910 |
rs760065718 | snp | A/G | 8.52842e-05 | 0.00652954 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486048 | AGCATCCTGAGCAGC[A/G]TGGATGCTGAGAATG | 89910 |
rs760078845 | snp | C/T | 0.000183509 | 0.0095771 | intron-variant, synonymous-codon, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491023 | GATATCATCCTCTGA[C/T]CAATTAAAACATTCT | 89910 |
rs760096558 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497863 | TCTGATTCGGCCGTT[C/G]CTCATCCACATCATG | 89910 |
rs760147611 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504189 | TGGCCCATTCTTTGT[C/T]ATGAGGGGCTGTCTT | 89910 |
rs760171800 | snp | A/C/G | 0.000322596 | 0.012697 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477282 | AGTCGGAGGACGCAG[A/C/G]AGTCTCCAAACCCGG | 89910 |
rs760183296 | snp | A/C | 3.29815e-05 | 0.00406075 | intron-variant | UBE3B | GRCh38.p7 | 12:109533418 | AAGGGCCCGTCCTGG[A/C]AGAGCAGGAGCCTGC | 89910 |
rs760189196 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539871 | GCAGCTCCTCCACCC[A/G]GGGACCAGCAGTTGC | 89910 |
rs760207401 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479069 | GTCTAGACTGGAGTA[A/G]ATGAGATCATGAATG | 89910 |
rs760211645 | snp | A/G | 4.94181e-05 | 0.00497057 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503097 | GGGGGTAAACGGGTC[A/G]ACTCTGCAGAAGTCC | 89910 |
rs760222552 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534291 | AGTTTTTACAGCATT[C/T]TACTTTTTGTCAATT | 89910 |
rs760286478 | snp | C/G | 3.30142e-05 | 0.00406276 | intron-variant | UBE3B | GRCh38.p7 | 12:109502991 | GCAGCTGGCTGAGCT[C/G]CTGCTCACATGTCTT | 89910 |
rs760359697 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493226 | CCCTACCCAAGTCAC[C/G]TTGTGGGGCAGCTCA | 89910 |
rs760370471 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | UBE3B | GRCh38.p7 | 12:109497812 | AGTGGATCTATCTGT[A/G]TCTAGCCCTGTGATT | 89910 |
rs760423512 | snp | A/G | 6.58903e-05 | 0.00573941 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497878 | CCTCATCCACATCAT[A/G]TCTGTGCCTGCTCTG | 89910 |
rs760450811 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511437 | AGGAAACGGTGGTTG[C/T]TATTACTTTGGTGAG | 89910 |
rs760461659 | snp | C/T | 6.69187e-05 | 0.00578402 | intron-variant | UBE3B | GRCh38.p7 | 12:109533832 | TGGGTACGTGCTGTT[C/T]TTAGTGGCGTCTGGC | 89910 |
rs760479443 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529581 | AGGGCCCTCTTCTTA[C/G]GTGGGGAATGTCTCC | 89910 |
rs760500457 | snp | A/C | 1.64906e-05 | 0.00287142 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524440 | TCTGTTACATTAGCG[A/C]TATGATGGGGACATC | 89910 |
rs760512064 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488665 | AAAATTCTTCGGGGA[A/G]AAGGTCTGTGGGACT | 89910 |
rs760514777 | snp | A/G | 1.81787e-05 | 0.0030148 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534548 | CAGCCTGGGCTCCCA[A/G]ACTAGGCCCTTCCCA | 89910 |
rs760555555 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493999 | ATTTTTTTATTTTTA[A/T]AATTTTTGTAGAGAC | 89910 |
rs760555647 | snp | C/T | 1.67144e-05 | 0.00289084 | intron-variant | UBE3B | GRCh38.p7 | 12:109524527 | GCCCTTTGGCTGAGC[C/T]CCCTTTCCACTGCCC | 89910 |
rs760563449 | snp | C/T | 1.69006e-05 | 0.00290689 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477221 | CCCAGCTCCCTCGGC[C/T]GCCCTCAACCCCTAG | 89910 |
rs760610712 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518294 | CCAGAAGAGGCCACC[A/G]CCACTCAGCTCCTCC | 89910 |
rs760612419 | snp | A/T | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499750 | ATGTGTCTCAGAAGA[A/T]GTCCAACCTGACCCA | 89910 |
rs760636375 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540757 | CTCACACAGAGTCCT[A/G]AACTAGCCTGCCTTA | 89910 |
rs760666371 | snp | G/T | 1.75496e-05 | 0.00296217 | intron-variant | UBE3B | GRCh38.p7 | 12:109511333 | GAGCTGGGCCCCGAT[G/T]TGTCTTTCTATTCCC | 89910 |
rs760671084 | snp | A/G | 1.726e-05 | 0.00293763 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499668 | TCCCTCAGCCCCAGA[A/G]TGTTAGAGGAGGAGA | 89910 |
rs760671236 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485934 | CACGTGCCAGGTACC[C/T]GCTGAAGGCTTGTTT | 89910 |
rs760781352 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476149 | AGAATGTCTGATTCA[G/T]TAGTCTCTGACAGGG | 89910 |
rs760808934 | snp | C/T | 1.65053e-05 | 0.0028727 | intron-variant | UBE3B | GRCh38.p7 | 12:109501360 | ACCAGGTCTCCTCTG[C/T]TCTCTCCTAGCCTTA | 89910 |
rs760830161 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494819 | TCCTATAATGCTTCC[A/G]CTGATACGTCGCTCC | 89910 |
rs760858025 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507026 | AGCTGTCTGAACCTC[A/G]TCTGGTTCTGAGGGC | 89910 |
rs760864407 | in-del | -/GTGA | 1.67149e-05 | 0.00289087 | splice-donor-variant | UBE3B | GRCh38.p7 | 12:109511304 | ATCCCTCACAAAAAC[-/GTGA]GTTGCACTCAGAGCT | 89910 |
rs760870790 | in-del | -/ACAAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491440 | TTGAAGTTTTAATTG[-/ACAAA]ACAAAAAACCTAGGA | 89910 |
rs760873554 | snp | C/T | 4.94173e-05 | 0.00497053 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109529987 | CGTTCCATTATCAAA[C/T]CCGAGTGGATCCGAA | 89910 |
rs760885344 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482924 | CAATATAATGGACTG[A/T]CTTGCATTCTGAAGT | 89910 |
rs760911449 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507880 | GAACTAGCCATTTAC[C/G]AAGTGAGCAGTGTGC | 89910 |
rs760926780 | snp | G/T | 1.64836e-05 | 0.0028708 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530060 | ATGCTGAGATTGATC[G/T]GGAAGATTTAAAGTA | 89910 |
rs760928630 | snp | G/T | 1.66515e-05 | 0.00288539 | splice-donor-variant | UBE3B | GRCh38.p7 | 12:109516885 | TCCAGGATGCTGGAG[G/T]TGAGTGTGAAGCCTA | 89910 |
rs760931393 | snp | C/T | 0.000281334 | 0.011857 | synonymous-codon, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490507 | CTGTGATGGGCTGTT[C/T]CCTGATTTGGTTTCA | 89910 |
rs760940529 | snp | A/G | 3.47608e-05 | 0.00416884 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521457 | CAACCAGTGGGGATG[A/G]GAGGCTGTACCCCTC | 89910 |
rs760954403 | in-del | -/ATGC | 1.65445e-05 | 0.00287611 | intron-variant | UBE3B | GRCh38.p7 | 12:109530676 | TTTTATTTATTACCT[-/ATGC]ATGCATGCATGCATG | 89910 |
rs760955545 | snp | G/T | 0.000121178 | 0.00778293 | intron-variant | UBE3B | GRCh38.p7 | 12:109507520 | AAATAACAGACCAGG[G/T]GGAGTCTCCACCTGA | 89910 |
rs760966447 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495628 | CAGAGATTTACCCAC[A/G]TATTTACTGACAGCA | 89910 |
rs760975776 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477467 | CTCCCCGGCCGGAGT[A/G]GGTTCCAGCTTTTCT | 89910 |
rs760978729 | snp | G/T | 4.96528e-05 | 0.00498236 | intron-variant | UBE3B | GRCh38.p7 | 12:109521114 | TGCATAAGGCTTTGG[G/T]CTTCCTAATGGGCTG | 89910 |
rs760993283 | snp | C/G | 1.71355e-05 | 0.00292702 | intron-variant | UBE3B | GRCh38.p7 | 12:109483724 | TCAGGTAAGGGCTAG[C/G]ATCTCCCTAGCACAT | 89910 |
rs761019034 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511750 | CAAGGCTGGGAGCAA[C/G]GGCTTTCTGCAAAGC | 89910 |
rs761058108 | snp | G/T | 1.66211e-05 | 0.00288275 | intron-variant | UBE3B | GRCh38.p7 | 12:109486449 | TAACAGCCCATGACA[G/T]TCCTCTTTTTCCCAC | 89910 |
rs761093675 | snp | C/T | 4.9445e-05 | 0.00497193 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533491 | GCTGCTCCAGACCCC[C/T]GCTCCTGGGATTCGC | 89910 |
rs761098287 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514821 | TTCTACTCAGAGCAC[A/G]TCAGTCCTGTCACGT | 89910 |
rs761113303 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536675 | TGAGATGTGATCAAA[A/G]GCTTTATTAAATTTG | 89910 |
rs761146816 | snp | C/G | 1.737e-05 | 0.00294698 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521545 | GCTGGGGAAGGCTGT[C/G]TATGAGGTAGGAACG | 89910 |
rs761168491 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525403 | CTCTACAGAATAGCT[C/T]ACGGGCAGGGTGTTC | 89910 |
rs761179245 | snp | G/T | 5.87354e-05 | 0.00541888 | intron-variant | UBE3B | GRCh38.p7 | 12:109510479 | CTCCAGGGGTGAGGA[G/T]GGCTCCATGGAAGCC | 89910 |
rs761182997 | snp | C/T | 3.52032e-05 | 0.00419528 | intron-variant | UBE3B | GRCh38.p7 | 12:109499836 | GATGCAAATCACTGT[C/T]TTTCCTGCCTCTCTC | 89910 |
rs761204135 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513142 | GGCTCCAGCCTTCAT[C/T]TCCTGGGCCTCATCT | 89910 |
rs761259258 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500551 | AAGACTCATTGCTAG[A/G]GAACAGCCTGCCCCA | 89910 |
rs761302056 | in-del | -/GA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538518 | CCCTCCAGAGCACGT[-/GA]GAGGATTAAATGCAG | 89910 |
rs761312022 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541946 | TCTCATCTTGTGGTC[C/G]TTACCTTAATTACAT | 89910 |
rs761353560 | snp | A/G | 1.64955e-05 | 0.00287184 | intron-variant | UBE3B | GRCh38.p7 | 12:109497959 | CCCCGTGAAAACCCA[A/G]TTGTGTTTTTCTTTT | 89910 |
rs761373980 | snp | A/G | 6.06275e-05 | 0.00550546 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510423 | CGAGCGGGACTGCCG[A/G]CGGCGCTTCACCCCC | 89910 |
rs761383572 | snp | C/T | 1.65127e-05 | 0.00287334 | intron-variant | UBE3B | GRCh38.p7 | 12:109503221 | GGCATCTTCTTCACC[C/T]CTCACATTTGGCAGA | 89910 |
rs761457273 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497889 | TCATGTCTGTGCCTG[C/T]TCTGGTGACTCATCT | 89910 |
rs761489505 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479469 | GCCTAGAGAGGATAA[C/G]TAACTTGGCCAAATG | 89910 |
rs761499136 | snp | A/G | 8.42779e-05 | 0.00649091 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534646 | TCACCATCCGCAAGC[A/G]GGAGCCAGGCGGCCG | 89910 |
rs761505766 | snp | C/T | 8.89846e-05 | 0.00666966 | intron-variant | UBE3B | GRCh38.p7 | 12:109521559 | TGTATGAGGTAGGAA[C/T]GTTAAGAAACAGAGA | 89910 |
rs761507744 | snp | A/C/G | 3.32559e-05 | 0.00407763 | intron-variant | UBE3B | GRCh38.p7 | 12:109533581 | CACGGGGTGGGTGGG[A/C/G]AAGAGCCTTGACTTC | 89910 |
rs761541223 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522227 | TCACACCAGGTGGAT[C/T]GGAGCAGTCATCCTC | 89910 |
rs761560741 | snp | A/C/T | 3.29464e-05 | 0.00405861 | missense, synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524023 | TTCTTCCTGAGCCAA[A/C/T]TGCTTGGGCACCACC | 89910 |
rs761562452 | snp | C/T | 1.64982e-05 | 0.00287208 | intron-variant | UBE3B | GRCh38.p7 | 12:109526447 | AGGTTTTTAAGGTCA[C/T]CACTTGAAAAGACTT | 89910 |
rs761611113 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539034 | TGAGGTCAGGAGTTC[C/T]AGACCATCCTGGCCA | 89910 |
rs761632028 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109489945 | CGACCAGCGATGAAC[C/T]ACATTTGTGCAAATA | 89910 |
rs761656078 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514660 | GACTCCACATGACAA[A/G]CACCTGTTCTCAAAA | 89910 |
rs761677615 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517277 | CTGTGATTGTAGTAT[A/G]TAAGTGGAGTGGAGG | 89910 |
rs761700377 | snp | C/T | 1.64868e-05 | 0.00287109 | stop-gained, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516780 | AGAGTTCTACTGTTT[C/T]GAACCATGGTTACCA | 89910 |
rs761702500 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493380 | AGCACCTCACCTTTC[-/T]TACCTGTCCAGCATC | 89910 |
rs761725664 | in-del | -/AACAAAAA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486578 | CAAGCAGCTCAAGGT[-/AACAAAAA]AAAAAAAAAAAAAAA | 89910 |
rs761753347 | snp | C/T | 1.65422e-05 | 0.0028759 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516864 | ACTCACATCACCATC[C/T]GCCGGTCCAGGATGC | 89910 |
rs761755340 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503127 | CAGAAGGTTTGCAAC[A/G]TCTGTGTCCTCTACC | 89910 |
rs761767080 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109509461 | TATCATTTTATCTGT[A/T]GATTTTACAGTAAGT | 89910 |
rs761783792 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515014 | CACCTACCGGGTTCA[C/T]GCCATTCTCCTGCCT | 89910 |
rs761817304 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539741 | AGACGCTTTGGCTGA[C/T]GTTAACAGGACATCC | 89910 |
rs761818359 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496712 | TATGTTTAGATCCTT[C/T]GTCTACTTTTTAATT | 89910 |
rs761818585 | snp | A/C | 1.64825e-05 | 0.00287071 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491096 | TGTCTATCCAAAGGC[A/C]CTTTAACAGCAGCTT | 89910 |
rs761850046 | snp | A/G | 1.66266e-05 | 0.00288323 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483614 | CCGTCAGGCACGAGA[A/G]GAAAGGCTTGTGCAG | 89910 |
rs761865168 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497988 | TTCTTCTTAAACATT[A/G]GAAAGTAAAATGGCT | 89910 |
rs761941189 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529339 | TTGCTCTGACTTCCC[A/T]GTTGAGTCCACTCCT | 89910 |
rs761944023 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481894 | ACAATTACTTTTGTA[A/C]CAACCTAATACCTTC | 89910 |
rs761956004 | in-del | -/A | 0.000173747 | 0.00931897 | intron-variant | UBE3B | GRCh38.p7 | 12:109533769 | CAGCCCTCTCTCGGC[-/A]AGCCCCTTTCTCTTT | 89910 |
rs761962852 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505789 | TAAGTATCCTTCAGT[A/G]GCTCTGATGGAGTTC | 89910 |
rs761985355 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475875 | TTATAAGACAGCTAC[C/T]GCCAATTGCAACTTC | 89910 |
rs761992471 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518144 | TAATCTCCACTTCTG[C/T]GCCCTCCTGTTCTTG | 89910 |
rs762004822 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483892 | TTTTTTAAAGCAGAT[A/G]ACCCTGAGTCCACTA | 89910 |
rs762033971 | snp | A/C | 1.72534e-05 | 0.00293708 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509758 | GGTTGATGCTGCACC[A/C]AGGGAGGCCGAAGAG | 89910 |
rs762052515 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521237 | CCTCGGGGTGGACGA[A/G]GCAGGGATTGATCAA | 89910 |
rs762083867 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507637 | GCCCCACGGAGGGTT[A/G]AAGCTCTTCTTGGAA | 89910 |
rs762136971 | snp | C/T | 1.74983e-05 | 0.00295784 | intron-variant | UBE3B | GRCh38.p7 | 12:109509549 | GATTTTTTTTCTCTT[C/T]GCCTTTTTTCAGTGT | 89910 |
rs762240756 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525283 | TCTGAGAAGCCTGTA[A/G]GGAGGAAACCAAAGT | 89910 |
rs762251221 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501442 | CTCTGATCCGGATCT[C/T]CTTCTGTGACATCCT | 89910 |
rs762293216 | snp | A/G | 3.2447e-05 | 0.00402771 | intron-variant | UBE3B | GRCh38.p7 | 12:109510491 | GGAGGGCTCCATGGA[A/G]GCCAGCCTGCTCCGG | 89910 |
rs762344319 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524865 | GCGCCTCAAGCTCAA[A/G]CAGAAGCCTGTCCTT | 89910 |
rs762367102 | in-del | -/AC | 1.68221e-05 | 0.00290014 | intron-variant | UBE3B | GRCh38.p7 | 12:109516933 | GAAGTGGGCCCTGCA[-/AC]ATGGAAGCTCTTTAG | 89910 |
rs762374079 | snp | C/T | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536651 | TGTTTTTGTAGCTAA[C/T]TTATGGATTGAGATG | 89910 |
rs762383336 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498254 | ACTGTTTTAGAATCC[C/T]ATGACATGCTTCGTA | 89910 |
rs762408364 | snp | C/T | 0.000149131 | 0.00863385 | intron-variant | UBE3B | GRCh38.p7 | 12:109533733 | GAGAACCAGCCAGCC[C/T]CAGAGAGACTGCCCA | 89910 |
rs762412388 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540940 | CCCACGCAAGAAGTG[C/T]GGTGGGCGGGAGCTG | 89910 |
rs762458401 | snp | C/T | 1.71546e-05 | 0.00292865 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486571 | ATTTTCTCAAGCAGC[C/T]CAAGGTAACAAAAAA | 89910 |
rs762521856 | snp | C/G | 1.69789e-05 | 0.00291362 | intron-variant | UBE3B | GRCh38.p7 | 12:109533612 | CCTCTTGGTGGTTGT[C/G]TGCTGTGCCCACTGT | 89910 |
rs762569322 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500273 | TATGAACTTAAAAAC[A/C]TGAGAAACACTAGAC | 89910 |
rs762580572 | snp | A/G | 4.94442e-05 | 0.00497188 | intron-variant | UBE3B | GRCh38.p7 | 12:109488547 | AAGACGTGTGTCTTA[A/G]TCTTGCTGTGTTTAT | 89910 |
rs762589832 | snp | C/T | 0.000142197 | 0.00843079 | intron-variant | UBE3B | GRCh38.p7 | 12:109490471 | AAGTAATGTTGACTT[C/T]GCCCTTCCTTCTCCC | 89910 |
rs762617907 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541691 | AAATGTATTCTCCTC[A/G]GACAGTTCTGGCCAG | 89910 |
rs762647795 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497401 | ACTGAATTATGAGTT[A/T]TTGGTGAGTTACCAC | 89910 |
rs762675211 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532151 | CCTGAATTTGCAGCG[A/G]GCAGACCTGAGCCGG | 89910 |
rs762718540 | snp | C/T | 1.65529e-05 | 0.00287683 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516867 | CACATCACCATCCGC[C/T]GGTCCAGGATGCTGG | 89910 |
rs762730707 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537906 | AGACAGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 89910 |
rs762746894 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478022 | GGGTGATTTGTTCCT[A/G]TGGTTGTTGATGCCG | 89910 |
rs762844974 | in-del | -/AACAAAAAA | 0.000749991 | 0.0193503 | intron-variant | UBE3B | GRCh38.p7 | 12:109486578 | CAAGCAGCTCAAGGT[-/AACAAAAAA]AAAAAAAAAAAAAAA | 89910 |
rs762902019 | snp | C/T | 4.97063e-05 | 0.00498505 | intron-variant | UBE3B | GRCh38.p7 | 12:109497974 | ATTGTGTTTTTCTTT[C/T]CTTCTTAAACATTAG | 89910 |
rs762914152 | in-del | -/TGGGG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487048 | ATCCCTGCTCCCTTT[-/TGGGG]TGGGGTCACCTCGTC | 89910 |
rs762930425 | in-del | -/T | 1.64764e-05 | 0.00287018 | intron-variant | UBE3B | GRCh38.p7 | 12:109489910 | GTTCTCACTGTTTTC[-/T]TTCTTTAGGTGAAAG | 89910 |
rs762954618 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522162 | GCCACATTCCTGGGT[C/T]GCCGTTAATGGTAAG | 89910 |
rs762970554 | snp | A/G | 1.70301e-05 | 0.00291801 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483706 | GTCGACTGCAGAGAG[A/G]TATCAGGTAAGGGCT | 89910 |
rs762971990 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507625 | CTGTGAGCTCGGGCC[C/T]CACGGAGGGTTAAAG | 89910 |
rs763004002 | snp | A/G/T | 8.62249e-05 | 0.00656554 | intron-variant | UBE3B | GRCh38.p7 | 12:109509560 | TCTTCGCCTTTTTTC[A/G/T]GTGTGGAATTGTGGG | 89910 |
rs763005158 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109509414 | TGTCCTAAGGCTCTC[A/C]CTCCCCTTTCCCCCT | 89910 |
rs763023000 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496583 | TTTAGCCATCCCAGT[A/G]GCTGTACAGGGGTAT | 89910 |
rs763122140 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485772 | GTTTTTATGTGAAGT[A/G]TACCAGTTTCTAAAA | 89910 |
rs763145273 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527088 | GGGGCAGATCATTTT[A/G]GATGATAGCACGTGG | 89910 |
rs763169673 | snp | A/C | 5.42363e-05 | 0.00520723 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534561 | CAAACTAGGCCCTTC[A/C]CAATTCAAGGCCACG | 89910 |
rs763219513 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485317 | GGCCCTTGGGAGGAA[A/G]CAGGACGGGCAAGAT | 89910 |
rs763347451 | in-del | -/CCACCTCCT | 1.68425e-05 | 0.00290189 | cds-indel, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534667 | CAGGCGGCCGCCTGC[-/CCACCTCCT]CCACCTGCTTCAACC | 89910 |
rs763349602 | snp | C/G/T | 3.30274e-05 | 0.0040636 | intron-variant | UBE3B | GRCh38.p7 | 12:109502983 | GGGATTTGGCAGCTG[C/G/T]CTGAGCTGCTGCTCA | 89910 |
rs763376287 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521286 | TTCTTGGAAGAGATC[A/C]TCAAGAGAGTTTTTG | 89910 |
rs763443089 | snp | G/T | 1.64974e-05 | 0.00287201 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501489 | GAGAGCCAGGAGCCA[G/T]CCCACGCACAGCCAG | 89910 |
rs763445215 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518051 | CCCACTGGGCCCTGC[A/T]GGCCATGTGAAGGAG | 89910 |
rs763473603 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504420 | TTAGAGGTAGAAGAT[A/G]TGGGTCTTACTGGTA | 89910 |
rs763480991 | snp | C/G | 4.94605e-05 | 0.0049727 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483900 | AGCAGATGACCCTGA[C/G]TCCACTAAAAGAAGT | 89910 |
rs763493721 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542232 | CCTCACCCATGGCAG[A/T]CATTACTAATTGATT | 89910 |
rs763496381 | snp | C/T | 1.64849e-05 | 0.00287092 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491109 | GCACTTTAACAGCAG[C/T]TTTTTCTCTAGCGTT | 89910 |
rs763525719 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541710 | AGTTCTGGCCAGAAG[C/T]CTGAAATCAAGGTGC | 89910 |
rs763539973 | snp | A/G | 4.94279e-05 | 0.00497107 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497822 | TCTGTGTCTAGCCCT[A/G]TGATTGCTGCACAGT | 89910 |
rs763581345 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493403 | CCAGCATCCCTCCCC[G/T]GTCCTGGTGTGGTTG | 89910 |
rs763622935 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541006 | CTTCTCTGCACGTCT[C/G]TGGCTCCAGCGTCCC | 89910 |
rs763633854 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500336 | CATGAATTTGAAATA[C/T]CTACCTGAGCTGAGA | 89910 |
rs763647541 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512853 | CCTTCCTTGAGGGAG[C/T]CCCTGCTATGATGTC | 89910 |
rs763655323 | snp | A/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478032 | TTCCTGTGGTTGTTG[A/T]TGCCGAGGAAAGACT | 89910 |
rs763686790 | snp | A/G | 0.000675815 | 0.0183698 | intron-variant | UBE3B | GRCh38.p7 | 12:109488718 | AACATTTCCATAGAG[A/G]GCTCAGGGACCTTTT | 89910 |
rs763783737 | snp | C/T | 0.000248437 | 0.0111426 | intron-variant | UBE3B | GRCh38.p7 | 12:109486081 | CCTAAGGTAAGTGGA[C/T]GGGAGCCGCAGTGTC | 89910 |
rs763834013 | snp | A/G | 6.59609e-05 | 0.00574248 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524442 | TGTTACATTAGCGCT[A/G]TGATGGGGACATCAC | 89910 |
rs763874814 | snp | C/G | 3.29495e-05 | 0.00405877 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109489925 | TTTCTTTAGGTGAAA[C/G]TCTTCGACCAGCGAT | 89910 |
rs763884868 | snp | C/T | 8.23676e-05 | 0.00641693 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109489937 | AAAGTCTTCGACCAG[C/T]GATGAACCACATTTG | 89910 |
rs763887553 | snp | C/T | 3.3521e-05 | 0.00409382 | intron-variant | UBE3B | GRCh38.p7 | 12:109524534 | GGCTGAGCTCCCTTT[C/T]CACTGCCCCCATGGG | 89910 |
rs763894625 | snp | A/G | 8.24097e-05 | 0.00641857 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533492 | CTGCTCCAGACCCCC[A/G]CTCCTGGGATTCGCC | 89910 |
rs763902249 | snp | A/C | 1.81556e-05 | 0.00301288 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534552 | CTGGGCTCCCAAACT[A/C]GGCCCTTCCCAATTC | 89910 |
rs763908760 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520128 | TTCATAGGACAGCAG[C/G]GTTGATTGGTCACTT | 89910 |
rs763945989 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512060 | GGACTGGGACATGGC[A/G]GCGAGTTCAGCATCG | 89910 |
rs763962038 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520894 | TGTCTAACTTCCCCA[C/T]CTCACTGCTCTGTCC | 89910 |
rs763985931 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant | UBE3B | GRCh38.p7 | 12:109488688 | GTGGGACTTGCTTCA[A/G]AATGTTCTCTAACCA | 89910 |
rs764002238 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479160 | AATGGGCACTCATTT[A/G]CTTTTTTAAATGATC | 89910 |
rs764009074 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508469 | CCATTTAGTTCCTTT[G/T]GTTTTTAAGCTTATG | 89910 |
rs764107428 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515520 | GATTACAGGCATGTG[C/T]CACCACGCCCAGCTA | 89910 |
rs764114695 | in-del | -/G | 5.23373e-05 | 0.00511526 | intron-variant | UBE3B | GRCh38.p7 | 12:109499842 | ATCACTGTCTTTCCT[-/G]GCCTCTCTCCCACCA | 89910 |
rs764116774 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480109 | GAAAAAAGTTAATGG[A/G]TGAGAAATGTCAGAC | 89910 |
rs764126226 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485319 | CCCTTGGGAGGAAAC[A/C]GGACGGGCAAGATCT | 89910 |
rs764128873 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539006 | TTTGGGAGGCTGAGG[C/T]GGGCAGATCCCCTGA | 89910 |
rs764141298 | snp | C/T | 1.6504e-05 | 0.00287258 | intron-variant | UBE3B | GRCh38.p7 | 12:109501362 | CAGGTCTCCTCTGCT[C/T]TCTCCTAGCCTTAAC | 89910 |
rs764200313 | in-del | -/TT | 3.5407e-05 | 0.0042074 | intron-variant | UBE3B | GRCh38.p7 | 12:109511338 | GGGCCCCGATGTGTC[-/TT]TCTATTCCCCCACGT | 89910 |
rs764202583 | snp | C/T | 0.000140677 | 0.00838561 | synonymous-codon, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490555 | CCCTGTGAGGTGGTC[C/T]GTTGGCAGAAGCTGG | 89910 |
rs764225543 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109529990 | TCCATTATCAAACCC[A/G]AGTGGATCCGAATGT | 89910 |
rs764226004 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484373 | GGGAGCAGCTACTAC[A/G]CACCTCGGTGGTGGA | 89910 |
rs764278964 | snp | G/T | 0.000152 | 0.00871647 | intron-variant | UBE3B | GRCh38.p7 | 12:109516892 | TGCTGGAGGTGAGTG[G/T]GAAGCCTATGGAATC | 89910 |
rs764278999 | snp | C/G | 1.67061e-05 | 0.00289011 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483666 | GTTGTGATCCAGGCC[C/G]ATGTCCGGAGTTTTC | 89910 |
rs764287974 | snp | C/T | 1.72952e-05 | 0.00294063 | intron-variant | UBE3B | GRCh38.p7 | 12:109507526 | CAGACCAGGTGGAGT[C/T]TCCACCTGAAGCTTG | 89910 |
rs764313914 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517422 | TCTGGAACTACCACT[A/C]TACGGTGACTCCATG | 89910 |
rs764377857 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534347 | CGGAAGGCCCCATTT[C/G]CAAAAGCTTACTTAG | 89910 |
rs764517825 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494967 | TTTCCTTGCAAATGC[A/G]AAGTGACTGGTTGTA | 89910 |
rs764552728 | snp | C/T | 1.65625e-05 | 0.00287766 | intron-variant | UBE3B | GRCh38.p7 | 12:109486460 | GACATTCCTCTTTTT[C/T]CCACCTATAGGTGTG | 89910 |
rs764643415 | snp | A/T | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497890 | CATGTCTGTGCCTGC[A/T]CTGGTGACTCATCTC | 89910 |
rs764646552 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480841 | AATTTCAGTACCTCA[A/C]AACAGCCACTGGTAA | 89910 |
rs764646560 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493469 | AGTCATTCTACCACA[C/T]TTAAATTCTCCTTTA | 89910 |
rs764690321 | snp | A/G | 3.30126e-05 | 0.00406266 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486473 | TTCCCACCTATAGGT[A/G]TGGTATGTGTCCCTG | 89910 |
rs764697868 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481785 | GCAGGAAGCGTAAAT[G/T]ATTCAGAAGATGGCT | 89910 |
rs764717237 | snp | C/T | 1.65239e-05 | 0.00287431 | intron-variant | UBE3B | GRCh38.p7 | 12:109503224 | ATCTTCTTCACCTCT[C/T]ACATTTGGCAGACAG | 89910 |
rs764759169 | snp | G/T | 3.30912e-05 | 0.00406749 | intron-variant | UBE3B | GRCh38.p7 | 12:109529853 | GCCTGCCCCGTCCTG[G/T]TAATTGTCATTGTTA | 89910 |
rs764784943 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524842 | AAGGGGAAGATGCCA[A/C]CTGAGAAGCGCCTCA | 89910 |
rs764799890 | snp | C/G | 1.64866e-05 | 0.00287106 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533507 | GCTCCTGGGATTCGC[C/G]TACCTCAAGCCTCCA | 89910 |
rs764802635 | in-del | -/AAAAT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109492757 | AAAAAAAAAAAAGTC[-/AAAAT]AAAAGGGAAATTTAG | 89910 |
rs764845806 | snp | C/T | 4.94882e-05 | 0.0049741 | intron-variant | UBE3B | GRCh38.p7 | 12:109497960 | CCCGTGAAAACCCAA[C/T]TGTGTTTTTCTTTTC | 89910 |
rs764853776 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540915 | AGGAGGTATGAGAGC[A/G]GCTCTGGGACCCACG | 89910 |
rs764933358 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487882 | CTCAGTGGTCTCCAA[A/G]GTTGTCTCCAAGGTC | 89910 |
rs764990817 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476469 | TACTCAGGGAACAGA[A/C]CCTTGAGGATCCCAA | 89910 |
rs765037011 | snp | A/T | 3.29451e-05 | 0.00405851 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530003 | CCGAGTGGATCCGAA[A/T]GTTCTCAACTCCTGA | 89910 |
rs765050840 | snp | A/T | 1.6501e-05 | 0.00287232 | intron-variant | UBE3B | GRCh38.p7 | 12:109526452 | TTTAAGGTCACCACT[A/T]GAAAAGACTTCATTC | 89910 |
rs765096758 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503143 | TCTGTGTCCTCTACC[A/G]GACCTCGCTGACAAC | 89910 |
rs765099758 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519758 | ACTTAATGATTCTCA[A/G]ACTTTATGTACATAA | 89910 |
rs765118724 | snp | C/T | 3.29478e-05 | 0.00405867 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109489949 | CAGCGATGAACCACA[C/T]TTGTGCAAATATAAT | 89910 |
rs765124542 | snp | A/T | | | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488618 | CCCTGTACCTCACGA[A/T]GCTTGTCACCTTCAC | 89910 |
rs765159309 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507208 | CAGACCTGAGTTCTA[C/T]TCCTGGCTCTGACAT | 89910 |
rs765172123 | snp | C/T | 1.70177e-05 | 0.00291694 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477293 | GCAGGAGTCTCCAAA[C/T]CCGGACTGAGAGAGG | 89910 |
rs765181442 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477944 | CTCCAGGGGCTCTTT[C/T]CGCGGCCCTTTCCAC | 89910 |
rs765184613 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493703 | GTCTATAAAATCGTC[-/A]GTGGTGTGCCAAGAT | 89910 |
rs765189519 | in-del | -/TG | 1.76783e-05 | 0.00297302 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534577 | AATTCAAGGCCACGA[-/TG]TGTGTGCCTTCAGGA | 89910 |
rs765224973 | snp | C/T | 4.97888e-05 | 0.00498918 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483636 | CTTGTGCAGAAGGAA[C/T]GGGAGCGGGCAGCTG | 89910 |
rs765242327 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525797 | GAAAAGATAATGAAA[C/T]TTCTAACAAAAAAAA | 89910 |
rs765251487 | in-del | -/AAC | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486578 | CAAGCAGCTCAAGGT[-/AAC]AAAAAAAAAAAAAAA | 89910 |
rs765252784 | snp | C/G | 6.58892e-05 | 0.00573936 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521253 | GCAGGGATTGATCAA[C/G]ACGGTGTTTTTAAGG | 89910 |
rs765271130 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529115 | GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC | 89910 |
rs765290917 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494944 | GTACCCTTATAACAA[C/T]GCAGTCCTTTCCTTG | 89910 |
rs765294910 | snp | C/T | 0.000103001 | 0.00717564 | intron-variant | UBE3B | GRCh38.p7 | 12:109483730 | AAGGGCTAGGATCTC[C/T]CTAGCACATGATTCT | 89910 |
rs765313107 | snp | G/T | 1.64895e-05 | 0.00287132 | intron-variant | UBE3B | GRCh38.p7 | 12:109533432 | GAAGAGCAGGAGCCT[G/T]CCCCGTCCCCACTGA | 89910 |
rs765326926 | snp | A/G | 0.000131889 | 0.00811956 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521151 | TGCTCTTGGCAGGAC[A/G]GCTACGAGCAGCTTA | 89910 |
rs765346165 | snp | A/C | 1.64868e-05 | 0.00287109 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483894 | TTTTAAAGCAGATGA[A/C]CCTGAGTCCACTAAA | 89910 |
rs765371775 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538268 | TCTCGCCAAGCTTGG[C/T]GAGTAAATCCAGGAC | 89910 |
rs765426919 | snp | A/C | 6.58968e-05 | 0.00573969 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507639 | CCCACGGAGGGTTAA[A/C]GCTCTTCTTGGAATG | 89910 |
rs765442198 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527370 | TTGGCCCCCTTGTCA[G/T]TTTATCAATCTCCCG | 89910 |
rs765485228 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498294 | TATTTTTAAGAGACC[A/G]AGATCGATGCCGTGA | 89910 |
rs765491401 | snp | A/G | 6.98812e-05 | 0.00591064 | intron-variant | UBE3B | GRCh38.p7 | 12:109509550 | ATTTTTTTTCTCTTC[A/G]CCTTTTTTCAGTGTG | 89910 |
rs765499233 | snp | C/G | 0.00063454 | 0.0178008 | intron-variant | UBE3B | GRCh38.p7 | 12:109510498 | TCCATGGAAGCCAGC[C/G]TGCTCCGGCACGCTG | 89910 |
rs765556102 | snp | A/C | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501371 | TCTGCTCTCTCCTAG[A/C]CTTAACGAGTCAATG | 89910 |
rs765557907 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526959 | AGGCACCCAGGCCAC[A/G]GTGTTCTTAGGAGTT | 89910 |
rs765619240 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513637 | GAAAGTCAGGGAACC[A/G]CTGAGATAAATTGGA | 89910 |
rs765635423 | in-del | -/GAG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513332 | ATATTTTAAATTTCT[-/GAG]GAGAACACAGTGAGA | 89910 |
rs765671626 | snp | C/T | 0.000282845 | 0.0118888 | utr-variant-3-prime, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490642 | GCTTCTAAAATAATA[C/T]GATGTCTTTAAATTT | 89910 |
rs765722215 | snp | A/T | 1.66838e-05 | 0.00288818 | intron-variant | UBE3B | GRCh38.p7 | 12:109516905 | TGTGAAGCCTATGGA[A/T]TCCTACCACAAGGAA | 89910 |
rs765731676 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502349 | AGTGGCTTTCCTATC[A/G]CAGGGTCAGTAATGG | 89910 |
rs765751345 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477396 | CACTTCCGCCCCGCA[A/G]AGGGCAACGTCTTAA | 89910 |
rs765784818 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504286 | GCGTGACAGCCAAAC[A/G]TATCTTCAAATTTGG | 89910 |
rs765785230 | in-del | -/G | 4.94173e-05 | 0.00497053 | frameshift-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521240 | GGGGTGGACGAAGCA[-/G]GGGATTGATCAAGAC | 89910 |
rs765804274 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479734 | AACAGAAATCAACCA[A/G]TAACATTGCTGAAGG | 89910 |
rs765830183 | snp | A/G | 3.30557e-05 | 0.00406531 | intron-variant | UBE3B | GRCh38.p7 | 12:109530082 | TTTAAAGTAAGAGGC[A/G]GGTGGGGGGAAGGGT | 89910 |
rs765843494 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534304 | TTCTACTTTTTGTCA[A/G]TTGGTTAACCAGTAA | 89910 |
rs765868498 | snp | A/G | 2.56092e-05 | 0.00357826 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486573 | TTTCTCAAGCAGCTC[A/G]AGGTAACAAAAAAAA | 89910 |
rs765877749 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510642 | CGCTTCTGTTAAGAG[A/G]TGTTTACACCAAATA | 89910 |
rs765892898 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523878 | GGGCCTGGAAATGCC[A/G]ATGGCACCCCTGGGC | 89910 |
rs765905832 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491774 | GGTGGAACCAGCTTG[G/T]TGAAAGCTGCCTGCT | 89910 |
rs765915360 | snp | A/T | 1.648e-05 | 0.0028705 | intron-variant | UBE3B | GRCh38.p7 | 12:109488550 | ACGTGTGTCTTAATC[A/T]TGCTGTGTTTATTGT | 89910 |
rs765961457 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480723 | GGCTCCAACTCTGTG[A/T]GACTCCCAAAGCCCG | 89910 |
rs765961470 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517541 | GCTGGAACATGGTTG[G/T]CATAAACTTAACTAC | 89910 |
rs766009221 | snp | C/G/T | 8.18239e-05 | 0.00639582 | intron-variant | UBE3B | GRCh38.p7 | 12:109510509 | CAGCCTGCTCCGGCA[C/G/T]GCTGCCCGAGCACTC | 89910 |
rs766063381 | snp | A/G | 6.59294e-05 | 0.00574111 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501388 | TTAACGAGTCAATGC[A/G]CTTGATCACCAAACA | 89910 |
rs766065772 | snp | C/G | 3.29484e-05 | 0.00405871 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503155 | ACCAGACCTCGCTGA[C/G]AACTCTCACACAGAT | 89910 |
rs766067011 | snp | A/G | 3.30437e-05 | 0.00406457 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511238 | CTCTTCCAAGAACTC[A/G]ACAGGGACAGAAAAC | 89910 |
rs766180673 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539175 | CAGGAGGCGGAGGTT[A/G]CAATGAGCCAAGATC | 89910 |
rs766201735 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533529 | AAGCCTCCATTCTCC[A/G]TCCGCTGCGTGGAGG | 89910 |
rs766225438 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507228 | GGCTCTGACATACAG[A/G]CTGTGTGATTTGGGG | 89910 |
rs766230277 | snp | C/T | 1.65718e-05 | 0.00287848 | intron-variant | UBE3B | GRCh38.p7 | 12:109503240 | ACATTTGGCAGACAG[C/T]TTGTCTTAGCAAAAG | 89910 |
rs766239729 | in-del | -/GTC | | | intron-variant, cds-indel | UBE3B | GRCh38.p7 | 12:109534418 | CTTCTCTGGAAGCCA[-/GTC]GTCTTGTGTCTGGGG | 89910 |
rs766247245 | snp | C/T | 1.65894e-05 | 0.00288 | intron-variant | UBE3B | GRCh38.p7 | 12:109497975 | TTGTGTTTTTCTTTT[C/T]TTCTTAAACATTAGA | 89910 |
rs766274696 | snp | C/T | 1.66084e-05 | 0.00288165 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483642 | CAGAAGGAACGGGAG[C/T]GGGCAGCTGTTGTGA | 89910 |
rs766286662 | snp | G/T | 1.72561e-05 | 0.0029373 | intron-variant | UBE3B | GRCh38.p7 | 12:109533616 | TTGGTGGTTGTCTGC[G/T]GTGCCCACTGTGCAA | 89910 |
rs766316526 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494067 | CTGGCCTCAAGCGAT[C/T]CTCATGCCTCAGCCT | 89910 |
rs766321954 | in-del | -/C | 1.64955e-05 | 0.00287184 | intron-variant | UBE3B | GRCh38.p7 | 12:109490018 | GGTCTGTGACTCCTG[-/C]CCCCCCAGTGTGCAA | 89910 |
rs766384655 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536089 | CAGTGGCAGCAAAGC[A/G]GGGGCCACCCGTCTC | 89910 |
rs766397846 | snp | A/G | 1.66078e-05 | 0.00288161 | intron-variant | UBE3B | GRCh38.p7 | 12:109523932 | CAATCCAAACACTGC[A/G]TCAGAATCCTGGCTG | 89910 |
rs766425132 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506075 | AGCCATCAGGAAACA[A/C]ATTTAGAAAGTCCTC | 89910 |
rs766425808 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476227 | TGGGACCAGAGTTTG[A/T]GAACCACTGGTTTAT | 89910 |
rs766478816 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507055 | GCTGCCTGATGGATG[A/C]ATTGTTTTTTGCTCA | 89910 |
rs766533954 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494827 | TGCTTCCACTGATAC[A/G]TCGCTCCCAGTCAGG | 89910 |
rs766569002 | snp | A/T | 1.64855e-05 | 0.00287097 | intron-variant | UBE3B | GRCh38.p7 | 12:109526318 | GCTTTATTTCCCCAT[A/T]AGAGTCCTCCCTATT | 89910 |
rs766589314 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538859 | AGAAGGATCCAGCCA[A/G]GGCGTTTCCAGGCCC | 89910 |
rs766624227 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477018 | TACTCCGCAAGCCCA[A/G]ATGTGCTTCCCGGAT | 89910 |
rs766669065 | snp | A/C | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521158 | GGCAGGACGGCTACG[A/C]GCAGCTTAGGCAGCT | 89910 |
rs766678043 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536712 | AGCATATGATGGCTG[C/T]GTTCTGCATTTCATT | 89910 |
rs766695635 | snp | A/G | 0.00013192 | 0.00812049 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491119 | AGCAGCTTTTTCTCT[A/G]GCGTTACGGTGAGTA | 89910 |
rs766704021 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484156 | GCCCAGTGCTTTTAG[A/G]AATCTTTTCACATTG | 89910 |
rs766713911 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503654 | AATTCTTCGAAAACC[G/T]TATCTTTATTGGCTA | 89910 |
rs766730318 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500587 | ACACCTCAGCCTGAG[A/G]AGGATGGGGCGGAGG | 89910 |
rs766738175 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541060 | ATCCTTGCAGCTATG[C/T]AGCCTTGCGCTCCTG | 89910 |
rs766744394 | snp | C/T | 1.64879e-05 | 0.00287118 | intron-variant | UBE3B | GRCh38.p7 | 12:109530542 | CAGGTCTGTATTGCT[C/T]TCAGGAAGCACACAG | 89910 |
rs766761734 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483000 | GTGTGCTGTCACAAA[G/T]TATGCACTGGTAAAT | 89910 |
rs766815000 | in-del | -/TTTTGT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506342 | CCAAATCTGTTTTGT[-/TTTTGT]TTTTGTTTTTGTTTT | 89910 |
rs766818160 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525460 | GCTGATTCTTAAGGG[C/T]CCTTTCAGCTTTAAA | 89910 |
rs766836888 | snp | A/T | 3.30147e-05 | 0.00406279 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501493 | GCCAGGAGCCAGCCC[A/T]CGCACAGCCAGCATC | 89910 |
rs766861580 | snp | A/G | 3.29734e-05 | 0.00406025 | intron-variant | UBE3B | GRCh38.p7 | 12:109497781 | TTCTGGATGCACACG[A/G]AGACCTGTCTGAATG | 89910 |
rs766912979 | snp | C/T | 8.80398e-05 | 0.00663417 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486030 | TTTGAGAAGTTGTGT[C/T]GCAGCATCCTGAGCA | 89910 |
rs766924601 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514871 | TCAGCAAGATGCTTC[A/T]CTGAACAGTAGTTCC | 89910 |
rs766925509 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488821 | GGTGCTGACCATCAG[A/G]CTGCATCGCAGTATC | 89910 |
rs766932225 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541958 | GTCCTTACCTTAATT[A/G]CATCTACAAAGACCT | 89910 |
rs766938540 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521309 | AGTTTTTGACCCAGC[A/G]CTCAATCTGTTCAAG | 89910 |
rs766994173 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513689 | ATAGTAATCCCCACA[-/T]TTTTTTTTTTCTTTT | 89910 |
rs767067337 | snp | C/T | 1.69126e-05 | 0.00290792 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477213 | TGCTGCTGCCCAGCT[C/T]CCTCGGCCGCCCTCA | 89910 |
rs767112113 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109479551 | GACTTTTTCTGCTGC[G/T]CACAGCCTTTTCTTT | 89910 |
rs767142131 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522444 | AGCACAAGCCCAGCC[A/G]GTCTGTGTGGCCTTC | 89910 |
rs767155819 | snp | C/T | 1.65726e-05 | 0.00287855 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501520 | CATCCCCTCAGAATG[C/T]GCTCCCAGTGAAGAG | 89910 |
rs767161329 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480525 | ATGTGGTGGTATGTA[A/C]CTGTGGTCCCAGCTA | 89910 |
rs767193337 | snp | A/T | 1.65965e-05 | 0.00288062 | intron-variant | UBE3B | GRCh38.p7 | 12:109498193 | CTACAGGAAACTGTT[A/T]CTGGCAGTTTCTGAT | 89910 |
rs767195331 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109509490 | GTATCTCTACAAGAT[A/G]AAGCTTATTTCTCAA | 89910 |
rs767211061 | snp | A/G | 3.29913e-05 | 0.00406135 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491122 | AGCTTTTTCTCTAGC[A/G]TTACGGTGAGTAAGA | 89910 |
rs767212645 | snp | A/G | | | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508566 | TACAATGGACCTCAG[A/G]CAGTTATGTTCAGGC | 89910 |
rs767212715 | snp | A/G | 1.65105e-05 | 0.00287315 | intron-variant | UBE3B | GRCh38.p7 | 12:109502986 | ATTTGGCAGCTGGCT[A/G]AGCTGCTGCTCACAT | 89910 |
rs767247184 | snp | C/T | 1.90612e-05 | 0.00308711 | intron-variant | UBE3B | GRCh38.p7 | 12:109533638 | ACTGTGCAAGGCCCT[C/T]ATCTAGTCCATATCT | 89910 |
rs767299377 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529472 | ATTTTTTTCTATTTT[A/G]AAACTTATTAGAGGA | 89910 |
rs767360700 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524048 | ACCACCACAGCGTCT[C/T]CTATAGCTCGGTGGA | 89910 |
rs767374794 | snp | G/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498273 | ACATGCTTCGTAAAT[G/T]CATCATATTTTTAAG | 89910 |
rs767375004 | snp | A/G | 3.89082e-05 | 0.00441051 | intron-variant | UBE3B | GRCh38.p7 | 12:109510505 | AAGCCAGCCTGCTCC[A/G]GCACGCTGCCCGAGC | 89910 |
rs767408299 | snp | C/T | 3.29815e-05 | 0.00406075 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524438 | TCTCTGTTACATTAG[C/T]GCTATGATGGGGACA | 89910 |
rs767434071 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485342 | CAAGATCTCTACGCT[A/C]ATGGAGCTCATAGCC | 89910 |
rs767453922 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496713 | ATGTTTAGATCCTTC[A/G]TCTACTTTTTAATTG | 89910 |
rs767507051 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497989 | TCTTCTTAAACATTA[A/G]AAAGTAAAATGGCTT | 89910 |
rs767524666 | snp | A/G | 1.71855e-05 | 0.00293129 | intron-variant | UBE3B | GRCh38.p7 | 12:109499824 | GGGTGAGTCCCAGAT[A/G]CAAATCACTGTCTTT | 89910 |
rs767530818 | in-del | -/C | 0.000937002 | 0.0216246 | intron-variant | UBE3B | GRCh38.p7 | 12:109486580 | AGCAGCTCAAGGTAA[-/C]AAAAAAAAAAAAAAA | 89910 |
rs767551183 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482112 | CACTTATTAAATGCC[A/T]TTCAATAACACGTAA | 89910 |
rs767564044 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517515 | TTGGTACAAGACCGT[A/G]CCTCCAATCTGCTGG | 89910 |
rs767564175 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529366 | TCCTAGCCCAGCTGC[A/G]TGTTTAAAGCATCTG | 89910 |
rs767577929 | snp | A/G | 4.96899e-05 | 0.00498422 | intron-variant | UBE3B | GRCh38.p7 | 12:109490033 | GCCCCCCAGTGTGCA[A/G]CTTCTCCACTCTCCA | 89910 |
rs767667166 | snp | G/T | 1.64757e-05 | 0.00287012 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109489987 | CTCAACCAGCATGGA[G/T]TTTATTCTGTGCTGC | 89910 |
rs767702458 | snp | A/C/G | 3.2961e-05 | 0.00405951 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516796 | GAACCATGGTTACCA[A/C/G]GGAGAAGGAGAAACT | 89910 |
rs767705265 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485921 | GGCATAATACCTGCA[C/T]GTGCCAGGTACCCGC | 89910 |
rs767721820 | snp | A/G | 1.65701e-05 | 0.00287833 | intron-variant | UBE3B | GRCh38.p7 | 12:109529842 | CATTGGTGACAGCCT[A/G]CCCCGTCCTGTTAAT | 89910 |
rs767791545 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477312 | GACTGAGAGAGGCAG[A/G]AAACACCCAGCTCAC | 89910 |
rs767796122 | in-del | -/GTGA | 1.64978e-05 | 0.00287205 | intron-variant, splice-donor-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491128 | TTCTCTAGCGTTACG[-/GTGA]GTAAGAAACCATAGC | 89910 |
rs767796302 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524872 | AAGCTCAAGCAGAAG[C/G]CTGTCCTTGTTCATT | 89910 |
rs767814601 | snp | C/T | 0.000170576 | 0.00923357 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486049 | GCATCCTGAGCAGCA[C/T]GGATGCTGAGAATGA | 89910 |
rs767814728 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494688 | CATGCTGGGGAAATC[A/G]GTAATAAGAAATTGA | 89910 |
rs767818877 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526648 | TAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG | 89910 |
rs767840192 | snp | C/T | 3.29598e-05 | 0.00405941 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521316 | GACCCAGCACTCAAT[C/T]TGTTCAAGGTATTTA | 89910 |
rs767855232 | snp | A/G | 1.72722e-05 | 0.00293867 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509760 | TTGATGCTGCACCCA[A/G]GGAGGCCGAAGAGTC | 89910 |
rs767891749 | snp | A/G | 1.71372e-05 | 0.00292717 | intron-variant | UBE3B | GRCh38.p7 | 12:109509577 | TGTGGAATTGTGGGT[A/G]ATTTTCTCTCTGATT | 89910 |
rs767893655 | snp | A/G | 1.73933e-05 | 0.00294895 | splice-acceptor-variant | UBE3B | GRCh38.p7 | 12:109521439 | GTCTTTTTGCCTTGC[A/G]GACAACCAGTGGGGA | 89910 |
rs767896553 | snp | C/T | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524057 | GCGTCTTCTATAGCT[C/T]GGTGGATGAACTGCC | 89910 |
rs767918868 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493634 | TAATTGAACACAATC[A/T]GGACCTTTTAAAGTA | 89910 |
rs767967416 | snp | C/T | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535947 | GTGTTGACAGCCACC[C/T]ACCCTCTCCCACCTC | 89910 |
rs767979699 | snp | G/T | 8.24219e-05 | 0.00641905 | intron-variant | UBE3B | GRCh38.p7 | 12:109497788 | TGCACACGGAGACCT[G/T]TCTGAATGAGTGGAT | 89910 |
rs768039127 | snp | A/G | 4.94588e-05 | 0.00497262 | intron-variant | UBE3B | GRCh38.p7 | 12:109497780 | GTTCTGGATGCACAC[A/G]GAGACCTGTCTGAAT | 89910 |
rs768091428 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514579 | GTGTATCACCAAACA[A/G]CACCCCTTCAGGTGG | 89910 |
rs768092150 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482865 | TTGGCAGGATGGTAA[G/T]TGTAAGGACAATGGA | 89910 |
rs768101373 | in-del | -/A | 5.03284e-05 | 0.00501614 | intron-variant | UBE3B | GRCh38.p7 | 12:109486423 | TAGAGCACAAGTGAT[-/A]ATGATCTCTATAACA | 89910 |
rs768107553 | snp | A/G | 6.74468e-05 | 0.00580679 | intron-variant | UBE3B | GRCh38.p7 | 12:109490138 | AGCTTGATGCCTGCT[A/G]TCCTCTTCTTCCTTC | 89910 |
rs768109633 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484639 | TTGTGATCTGCCCGC[C/T]TCAGCCTCCCAGAGT | 89910 |
rs768132757 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109529944 | CACTCAAATAAAAAA[A/C]CAAACAGCTGCCCTC | 89910 |
rs768138484 | snp | C/T | 1.65072e-05 | 0.00287286 | intron-variant | UBE3B | GRCh38.p7 | 12:109503215 | CCCCAGGGCATCTTC[C/T]TCACCTCTCACATTT | 89910 |
rs768162705 | snp | A/G | 0.000118707 | 0.00770322 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483694 | TTCTCTGTCGGAGTC[A/G]ACTGCAGAGAGATAT | 89910 |
rs768187824 | snp | C/T | 3.30131e-05 | 0.00406269 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516850 | CCTCCCCGCATGTCA[C/T]TCACATCACCATCCG | 89910 |
rs768240957 | snp | C/T | | | stop-gained, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501402 | CACTTGATCACCAAA[C/T]AGCTGCAGTTCTTGT | 89910 |
rs768309806 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516955 | AGCTCTTTAGTGGAC[A/G]GTCTCTGGCTTTTGA | 89910 |
rs768340824 | snp | A/G | 3.37467e-05 | 0.00410758 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534640 | GCTTCTTCACCATCC[A/G]CAAGCGGGAGCCAGG | 89910 |
rs768352464 | in-del | -/GTAC | 4.25822e-05 | 0.00461403 | intron-variant | UBE3B | GRCh38.p7 | 12:109486619 | GCAAAACCAGAAACA[-/GTAC]GTATGTCATTTTCAC | 89910 |
rs768406285 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478760 | CACTCCAGCCTGGGC[-/A]ACAAAGTGAGACTCC | 89910 |
rs768426032 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542648 | CAGAAAGAGAGGACT[C/T]GGCCATGTGAAGACA | 89910 |
rs768490349 | snp | G/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491213 | TCGTTACTGGTATTA[G/T]GTATAGACTTGCCCA | 89910 |
rs768502773 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539658 | TCATGGCTGTGATAA[C/T]TGTCATTATTTTGTT | 89910 |
rs768541955 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109492518 | AGACTGAGGTGGGCA[C/G]ATCATTTTGAGCTCA | 89910 |
rs768561722 | snp | A/G | 1.67511e-05 | 0.00289401 | missense, nc-transcript-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509705 | AAGATGATCTGGGAT[A/G]GAATTGTAGGTAAGA | 89910 |
rs768573518 | in-del | -/TG | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535931 | GCCCTGTTTGTGGTC[-/TG]TGTTGACAGCCACCC | 89910 |
rs768591150 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538389 | TCCAAGAAGCAGAGC[A/G]TGGGCTCTGGAATCG | 89910 |
rs768597417 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481374 | TTTAACATTCCATGA[C/T]CTCTAAGTTATTTTG | 89910 |
rs768598293 | snp | A/G | | | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530011 | ATCCGAATGTTCTCA[A/G]CTCCTGAACTGCAGC | 89910 |
rs768646478 | snp | G/T | 1.6492e-05 | 0.00287154 | intron-variant | UBE3B | GRCh38.p7 | 12:109526439 | TAGCAATTAGGTTTT[G/T]AAGGTCACCACTTGA | 89910 |
rs768659247 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476504 | ACAAACCCCACAGCT[A/G]AGAGACAGATCTTGA | 89910 |
rs768668323 | snp | C/T | 8.2689e-05 | 0.00642944 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499764 | AAGTCCAACCTGACC[C/T]ACTGGCATCCTGTCC | 89910 |
rs768767673 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487145 | GGAGGAGAGGCCTCC[C/T]GACCAGTTCAAAAAT | 89910 |
rs768803824 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540506 | ATGAGCCATTCACTG[C/T]ACCGGGCCCCCTATG | 89910 |
rs768820043 | snp | A/G | 3.43159e-05 | 0.00414207 | intron-variant | UBE3B | GRCh38.p7 | 12:109501578 | TAGCTCCACTTGGCT[A/G]AAGTACAGCTCCTGT | 89910 |
rs768821990 | snp | A/G | 1.64822e-05 | 0.00287068 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491086 | ACCCCGTCCTTGTCT[A/G]TCCAAAGGCACTTTA | 89910 |
rs768852371 | snp | A/G | 3.45596e-05 | 0.00415676 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510349 | TGTCCCACAGAGAAC[A/G]CCAAGGGTGAGACCT | 89910 |
rs768854577 | in-del | -/CCCCACTGA | 1.64876e-05 | 0.00287116 | intron-variant | UBE3B | GRCh38.p7 | 12:109533439 | AGGAGCCTGCCCCGT[-/CCCCACTGA]CCCTGCTTTGTGTTG | 89910 |
rs768879998 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485795 | TTCTAAAACATTTCT[A/G]TAGGGTTCCTCCAGC | 89910 |
rs768901588 | in-del | -/AG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508997 | GGTGTGAATTAAGAA[-/AG]TGTCACAGTCAGATC | 89910 |
rs768976555 | snp | A/G | 6.60404e-05 | 0.00574594 | intron-variant | UBE3B | GRCh38.p7 | 12:109524130 | GGTGAGCATGGAATG[A/G]TGGGTGAGCTAAGCC | 89910 |
rs768995826 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109530306 | GCTCTAGGAGATGGG[A/G]TCAGAGGATCTGGGG | 89910 |
rs769047912 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507553 | CTTGGGTTTCTCTGT[G/T]TTTTTTCCAGGTCTC | 89910 |
rs769063939 | snp | C/T | 1.66902e-05 | 0.00288874 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507572 | TTTCCAGGTCTCACT[C/T]ACCTTGATGACCTGC | 89910 |
rs769109805 | snp | A/T | 1.65897e-05 | 0.00288003 | intron-variant | UBE3B | GRCh38.p7 | 12:109533573 | GGTACCCCCACGGGG[A/T]GGGTGGGGAAGAGCC | 89910 |
rs769116854 | snp | A/C/T | 4.9482e-05 | 0.00497383 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498233 | TGCTATTCTTTGCAG[A/C/T]GCCTCACTGTTTTAG | 89910 |
rs769124539 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477336 | AGCTCACGCCAGCCG[A/G]GGGCGGAGGCGGGGC | 89910 |
rs769137229 | snp | G/T | 0.00014871 | 0.00862165 | intron-variant | UBE3B | GRCh38.p7 | 12:109510481 | CCAGGGGTGAGGAGG[G/T]CTCCATGGAAGCCAG | 89910 |
rs769175062 | snp | A/G | 7.32091e-05 | 0.00604973 | intron-variant | UBE3B | GRCh38.p7 | 12:109533696 | GAGCCAAGTGAGGAG[A/G]GCCCCACAGTTCTCA | 89910 |
rs769221797 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525237 | GGCCTGTCCTCCTGA[A/G]AGGCCCCTGGGCAGG | 89910 |
rs769242775 | snp | A/G | 4.50593e-05 | 0.00474632 | intron-variant | UBE3B | GRCh38.p7 | 12:109486623 | AACCAGAAACAGTAC[A/G]TATGTCATTTTCACC | 89910 |
rs769274251 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535901 | GAACTTTAGCTCCAG[A/G]GAACTGAGGCAGAGG | 89910 |
rs769334836 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507620 | TTTATCTGTGAGCTC[A/G]GGCCCCACGGAGGGT | 89910 |
rs769337515 | snp | C/T | 0.000330524 | 0.0128512 | intron-variant | UBE3B | GRCh38.p7 | 12:109517987 | GCAGTGTGTGCTGAA[C/T]AGTGGATGTTTCTGA | 89910 |
rs769361324 | in-del | -/TAAAA | 4.94662e-05 | 0.00497299 | intron-variant | UBE3B | GRCh38.p7 | 12:109489881 | AGGTCACATTATGGC[-/TAAAA]AAGAGACTTTTTTGT | 89910 |
rs769382022 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512707 | GTTCTGTCCTTGACT[C/T]TAATACTTATGGTTG | 89910 |
rs769390021 | snp | C/T | 1.64885e-05 | 0.00287123 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498236 | TATTCTTTGCAGCGC[C/T]TCACTGTTTTAGAAT | 89910 |
rs769441257 | snp | A/G | 4.94548e-05 | 0.00497242 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498340 | AGAAGGATGCCATAC[A/G]CTTTGTCTAATGGGT | 89910 |
rs769473261 | snp | A/G | 2.16144e-05 | 0.00328736 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510439 | CGGCGCTTCACCCCC[A/G]AGGACCACTGGCTGC | 89910 |
rs769483795 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482750 | AAAAAACAGTTACTG[A/G]TGATTTAGATAAAAA | 89910 |
rs769489654 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523642 | GGGGGTGCTGGTACT[A/G]TGCACGTTCCATCCT | 89910 |
rs769489667 | snp | C/T | 1.65119e-05 | 0.00287327 | intron-variant | UBE3B | GRCh38.p7 | 12:109483856 | TTTTGCACTTTCTTT[C/T]CTAGGAGAGAGATTG | 89910 |
rs769499813 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109529958 | ACCAAACAGCTGCCC[G/T]CATTAGCGGATTCCG | 89910 |
rs769501564 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542515 | AAGATGCATCCTAAC[A/C]CCCACTACCTCAGCA | 89910 |
rs769569204 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500265 | AGTGTAATTATGAAC[C/T]TAAAAACATGAGAAA | 89910 |
rs769575143 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514469 | GCCCTGTCCAGGCTT[A/T]CTGTGGTCACTTCTG | 89910 |
rs769577695 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489519 | GACCCTGGCCTCTTG[C/G]GGGGAACCCAAAAAT | 89910 |
rs769624231 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501088 | TGGGTACAAGATTGT[G/T]TTTGTCACCTGGGTG | 89910 |
rs769627108 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478921 | CAGCTTTTCCTACTG[C/T]ACAGGGACAATCCTC | 89910 |
rs769627314 | snp | C/G | 0.000143627 | 0.00847305 | intron-variant | UBE3B | GRCh38.p7 | 12:109533723 | CTCACGGCAGGAGAA[C/G]CAGCCAGCCCCAGAG | 89910 |
rs769627683 | snp | A/T | 1.69568e-05 | 0.00291172 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499807 | CCCAATCTGTGGATT[A/T]TGGGTGAGTCCCAGA | 89910 |
rs769709514 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530032 | GAACTGCAGCGTCTC[A/G]TCTCTGGCGACAATG | 89910 |
rs769736623 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532094 | TCCTCCGCCCCTCCC[C/T]GCTCGCAGGAGCGGG | 89910 |
rs769760194 | snp | A/T | 1.65135e-05 | 0.00287341 | intron-variant | UBE3B | GRCh38.p7 | 12:109502973 | TTTCCAGGGTGGGAT[A/T]TGGCAGCTGGCTGAG | 89910 |
rs769782398 | snp | A/G | | | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490925 | TAGGTACAAGCCACC[A/G]TGCCTGGCTCACAAT | 89910 |
rs769791757 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533017 | CCTCTGTTCGCACCA[C/T]GTGCAGTGGGTGCCA | 89910 |
rs769829361 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483504 | ACACAACAATCTACA[A/G]CACCCACTTGCCCAT | 89910 |
rs769962517 | snp | A/G | 1.76039e-05 | 0.00296676 | intron-variant | UBE3B | GRCh38.p7 | 12:109484021 | ATAATACTTCCATAT[A/G]TCAGATCTTTTATAA | 89910 |
rs769980608 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480319 | TCACATTTAGTCCTC[A/G]TTATCAACCTCTAAG | 89910 |
rs769983890 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109521997 | GTGGAGTTTGATAGT[C/T]TTAAAATCTTGTGTT | 89910 |
rs770005099 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496518 | GTAGTGTTGTGTGAG[G/T]TCTCCAGTTTCTCCA | 89910 |
rs770015961 | snp | A/G/T | 3.35454e-05 | 0.00409534 | intron-variant | UBE3B | GRCh38.p7 | 12:109486425 | AGAGCACAAGTGATA[A/G/T]GATCTCTATAACAGC | 89910 |
rs770019299 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497849 | CAGTTCTCAGACAAT[C/G]TGATTCGGCCGTTCC | 89910 |
rs770028750 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527797 | AGCCATTCCTTTAGG[C/G]GGGTGCTTGTAGGGC | 89910 |
rs770075084 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109530484 | CTGTCTGCATGACCT[A/G]CCTGCCTGTCCATAA | 89910 |
rs770110058 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510719 | ACATTTCTCATCCAA[A/G]CTAGGAAGAGGTCTT | 89910 |
rs770124611 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481241 | AGAATCGCTTGAACC[C/T]GGGAGCAGAAGTTAT | 89910 |
rs770198036 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485647 | AGTATCCATGGTGCT[C/T]AAGAAAAGGTAAACT | 89910 |
rs770202886 | snp | A/C/G | 0.000134907 | 0.00821191 | intron-variant | UBE3B | GRCh38.p7 | 12:109533835 | GTACGTGCTGTTTTT[A/C/G]GTGGCGTCTGGCCTC | 89910 |
rs770214667 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109509238 | CAAATCCTAGACATC[A/G]TATCATTTTTTTCAT | 89910 |
rs770217184 | snp | C/T | 1.69255e-05 | 0.00290903 | upstream-variant-2KB, missense, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477262 | CCGCCCTCCCTACCA[C/T]GAAAAGTCGGAGGAC | 89910 |
rs770252181 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488626 | CTCACGATGCTTGTC[A/G]CCTTCACAGACACTT | 89910 |
rs770253131 | in-del | -/AAACACCC | 1.71971e-05 | 0.00293227 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477313 | ACTGAGAGAGGCAGG[-/AAACACCC]AGCTCACGCCAGCCG | 89910 |
rs770253487 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486931 | TATCACGTACCAGTT[A/G]AGCAAGGAAGAGAAC | 89910 |
rs770263067 | snp | A/G | 0.00014885 | 0.00862571 | intron-variant | UBE3B | GRCh38.p7 | 12:109524146 | TGGGTGAGCTAAGCC[A/G]AGCACTGGTGTGAAC | 89910 |
rs770282528 | in-del | -/C | 1.64863e-05 | 0.00287104 | intron-variant | UBE3B | GRCh38.p7 | 12:109526312 | CGGGAAGCTTTATTT[-/C]CCCATTAGAGTCCTC | 89910 |
rs770282740 | snp | A/C | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501443 | TCTGATCCGGATCTT[A/C]TTCTGTGACATCCTG | 89910 |
rs770282819 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517927 | TGGAGAGCTTGTTTG[A/G]GTGCCCCTGGCCACT | 89910 |
rs770309975 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517135 | AGAGTATCCTGGGCT[A/G]GAGCATCCACCTCTT | 89910 |
rs770314364 | snp | A/G | 4.95454e-05 | 0.00497697 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524483 | CTGACGCTGTCTTAC[A/G]ACGAGGACGTCATGG | 89910 |
rs770345728 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518894 | TAATCTGGTGGCTTG[A/G]TTATTAGAATATGAG | 89910 |
rs770371345 | snp | A/G | 1.68476e-05 | 0.00290233 | intron-variant | UBE3B | GRCh38.p7 | 12:109511311 | ACAAAAACGTGAGTT[A/G]CACTCAGAGCTGGGC | 89910 |
rs770389235 | snp | C/T | | | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109544096 | CATTAAAGAAGAGAG[C/T]GAGCTGGTTCTTCTG | 89910 |
rs770423535 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481084 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 89910 |
rs770425940 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109543380 | CGGCACGGGGTCAGC[A/G]GCTGGTAACACAGCA | 89910 |
rs770427616 | snp | C/G | 1.65364e-05 | 0.0028754 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524488 | GCTGTCTTACGACGA[C/G]GACGTCATGGGTCAG | 89910 |
rs770448267 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109481681 | AGCTGTTCTCAGCCA[C/T]GAGTCCTGTGCAAGA | 89910 |
rs770449472 | snp | C/T | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535553 | CCTTAGCAGCAGCCC[C/T]GTTTCCAGAATGTGC | 89910 |
rs770460631 | snp | C/T | 1.65814e-05 | 0.00287931 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507728 | GACTGTTCGCGGCAC[C/T]TCATCACGTAGGTTG | 89910 |
rs770466164 | snp | A/G/T | 3.30236e-05 | 0.00406336 | intron-variant | UBE3B | GRCh38.p7 | 12:109498357 | TTTGTCTAATGGGTA[A/G/T]GTATCCGTGGCTGGA | 89910 |
rs770499603 | snp | C/G | 0.000247768 | 0.0111276 | intron-variant | UBE3B | GRCh38.p7 | 12:109524398 | CTTAAGCACATAGTG[C/G]TCCATGGCCCTAACA | 89910 |
rs770502621 | snp | C/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536441 | ACCAGTGAGGGACTG[C/G]GAGAGAGTGATTTAT | 89910 |
rs770520959 | snp | C/T | 1.84327e-05 | 0.00303579 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499647 | GGCAACCTCCTACAC[C/T]TGGGCTCCCTCAGCC | 89910 |
rs770557364 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505490 | ATAGGAGTATATTTG[C/T]GATCTCCACAGTGTT | 89910 |
rs770630390 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482682 | TCAATATGGGAGCCT[C/G]CGGGGGTCAGTGCTG | 89910 |
rs770640587 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479301 | TACATGCTTTTAGAT[A/T]TCCTATATTAATATT | 89910 |
rs770652239 | snp | C/T | 3.31301e-05 | 0.00406989 | intron-variant | UBE3B | GRCh38.p7 | 12:109521103 | CCCGAATTGTGTGCA[C/T]AAGGCTTTGGGCTTC | 89910 |
rs770676775 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512443 | TCCAGGAAATGAGGG[C/T]AGCAAGCATGGCTCA | 89910 |
rs770683123 | snp | A/C/T | 3.29643e-05 | 0.00405971 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491072 | CGTGGCCTGGCAAGA[A/C/T]CCCGTCCTTGTCTAT | 89910 |
rs770693481 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483443 | CTCTGCTGCCCAGGT[C/T]CCTGCCCACCCTCTG | 89910 |
rs770702927 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525043 | GCTCTGGGAGTGCAG[A/G]TCCAAGGGCCGCTCA | 89910 |
rs770705560 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507627 | GTGAGCTCGGGCCCC[A/G]CGGAGGGTTAAAGCT | 89910 |
rs770721812 | snp | A/T | 3.29728e-05 | 0.00406021 | intron-variant | UBE3B | GRCh38.p7 | 12:109499860 | CTCTCTCCCACCATC[A/T]TCTTCTTCCTTCTTT | 89910 |
rs770868206 | snp | C/G | 1.66123e-05 | 0.00288199 | intron-variant | UBE3B | GRCh38.p7 | 12:109530113 | GAAATTCCTTGGCCT[C/G]CCAGAAAGCCAGCTG | 89910 |
rs770894139 | in-del | -/C | 2.11786e-05 | 0.00325405 | frameshift-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510434 | GCCGGCGGCGCTTCA[-/C]CCCCGAGGACCACTG | 89910 |
rs770898948 | snp | C/T | 8.52043e-05 | 0.00652648 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483709 | GACTGCAGAGAGATA[C/T]CAGGTAAGGGCTAGG | 89910 |
rs770910131 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497859 | ACAATCTGATTCGGC[C/T]GTTCCTCATCCACAT | 89910 |
rs770918711 | snp | C/T | 1.68269e-05 | 0.00290055 | intron-variant | UBE3B | GRCh38.p7 | 12:109483994 | GAGGTAAAACGATAA[C/T]AGCAAACATGTATAA | 89910 |
rs770955936 | snp | C/T | 1.64931e-05 | 0.00287163 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483873 | TAGGAGAGAGATTGA[C/T]GACTTTTTTAAAGCA | 89910 |
rs770965255 | snp | C/G | 1.67424e-05 | 0.00289326 | intron-variant | UBE3B | GRCh38.p7 | 12:109486437 | ATATGATCTCTATAA[C/G]AGCCCATGACATTCC | 89910 |
rs771034258 | snp | C/G | 1.72136e-05 | 0.00293369 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521527 | CGAGTTTGTGGGGAA[C/G]ATGCTGGGGAAGGCT | 89910 |
rs771071865 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520632 | CCCATTACCTTCAGG[A/T]TGTCCCCTAAATTCC | 89910 |
rs771087203 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507977 | TGATCAGTACCACTG[A/G]CTGTGGCTTGGGGTC | 89910 |
rs771090476 | snp | A/G | 3.29516e-05 | 0.00405891 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497923 | CACAGTGACCCCTGA[A/G]GTAAGCAGGCTCTGT | 89910 |
rs771112628 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109516645 | CTGGTAGCACATGTT[A/C]AGGCATCCCATTCTG | 89910 |
rs771145796 | snp | A/C/G | 3.29599e-05 | 0.00405944 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486530 | TTGGATTCAACAGAT[A/C/G]AAGAACATTTTGTGG | 89910 |
rs771165448 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537993 | GGCGTGAGCCACCGC[A/G]CCCGGCCAACATTCT | 89910 |
rs771189120 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489348 | GTGGGGAGGCCTTGC[C/T]TGGTCTGGGTCTCTA | 89910 |
rs771191233 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477706 | ACTCGGGTGTTTTGG[A/G]CTGAGACAGTGGCAG | 89910 |
rs771201416 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487087 | CTGTAATCATGGCAA[C/T]GAGCAGTTTTGACTT | 89910 |
rs771222229 | in-del | -/C | 1.65348e-05 | 0.00287526 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483954 | CAGGAAACTGCTGTT[-/C]CTATTCAGAATCAAA | 89910 |
rs771285381 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508995 | GAGGTGTGAATTAAG[A/G]AAGTGTCACAGTCAG | 89910 |
rs771300927 | snp | G/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109526378 | TTGCCATGAACTGAT[G/T]CCTGGAGGGAAGACC | 89910 |
rs771384931 | snp | A/G | 3.3923e-05 | 0.0041183 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477273 | ACCATGAAAAGTCGG[A/G]GGACGCAGGAGTCTC | 89910 |
rs771385486 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497665 | CACTGACTTGTCCAT[C/T]TCCCCAGTGTATGTC | 89910 |
rs771411711 | snp | C/T | 3.37923e-05 | 0.00411036 | intron-variant | UBE3B | GRCh38.p7 | 12:109511314 | AAAACGTGAGTTGCA[C/T]TCAGAGCTGGGCCCC | 89910 |
rs771441016 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528827 | GCACTCCAGCATGGG[C/T]GACAAGAATGAAACT | 89910 |
rs771444497 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526732 | AAAAATTAGCTGGGC[A/G]TGGTGGCTCATGCCT | 89910 |
rs771450693 | snp | C/G | 1.65581e-05 | 0.00287728 | intron-variant | UBE3B | GRCh38.p7 | 12:109516733 | GTCAGTTTGCTGACC[C/G]TGTTTTCTGATCCCG | 89910 |
rs771495334 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527709 | GAGGGACTGCCTGCA[A/G]GAGTAGAGAGGGCCC | 89910 |
rs771497962 | snp | C/T | 1.65367e-05 | 0.00287543 | intron-variant | UBE3B | GRCh38.p7 | 12:109530674 | GTATTTTATTTATTA[C/T]CTATGCATGCATGCA | 89910 |
rs771505737 | snp | C/T | 4.94173e-05 | 0.00497053 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503081 | TATTCTCAGGCCTGT[C/T]GGGGGTAAACGGGTC | 89910 |
rs771514066 | in-del | -/CAC | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502627 | AGAACTAGAGGTTGT[-/CAC]GCCTTACTTCCCTCT | 89910 |
rs771525307 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109503784 | TTAGGTTGCAGCACA[A/G]TTGTTGTTATGAATT | 89910 |
rs771526956 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542752 | GAGAGGCTAGGAACA[A/G]ATTCTCCTTCACAGC | 89910 |
rs771547845 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505681 | TTATAACCACATCCT[A/C]CTACCCTTGAAAATG | 89910 |
rs771551150 | snp | A/G | 1.68983e-05 | 0.00290669 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534625 | GCAGCGTCCTCCGGG[A/G]CTTCTTCACCATCCG | 89910 |
rs771568927 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487110 | TTTGACTTTATATTC[-/T]TACTCTGTCTTGACT | 89910 |
rs771580274 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491412 | AGAGGCCAAGATGCA[A/G]TCATTTTTCCTTTTG | 89910 |
rs771603181 | snp | C/T | 1.7501e-05 | 0.00295807 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499662 | TTGGGCTCCCTCAGC[C/T]CCAGAGTGTTAGAGG | 89910 |
rs771664838 | snp | C/T | 3.29516e-05 | 0.00405891 | intron-variant | UBE3B | GRCh38.p7 | 12:109489912 | TCTCACTGTTTTCTT[C/T]CTTTAGGTGAAAGTC | 89910 |
rs771675959 | snp | A/C | 1.69812e-05 | 0.00291382 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477279 | AAAAGTCGGAGGACG[A/C]AGGAGTCTCCAAACC | 89910 |
rs771685459 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478762 | CTCCAGCCTGGGCAA[C/G]AAAGTGAGACTCCGT | 89910 |
rs771722819 | snp | A/G | 3.37798e-05 | 0.00410959 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483591 | AGAGCATGGTTCATC[A/G]ATAGAGCCCGTCAGG | 89910 |
rs771727612 | in-del | -/AG | 4.95569e-05 | 0.00497755 | frameshift-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511241 | TTCCAAGAACTCGAC[-/AG]GGACAGAAAACGGGC | 89910 |
rs771775987 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534136 | GATGCAGTTTGAGCC[C/T]GTGATGCCACCTTGT | 89910 |
rs771821223 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522908 | CCATTAGGACCCACC[C/T]GAGCACATGGCATAT | 89910 |
rs771844201 | snp | A/G | 3.30486e-05 | 0.00406487 | intron-variant | UBE3B | GRCh38.p7 | 12:109498366 | TGGGTAAGTATCCGT[A/G]GCTGGAACTTGATTG | 89910 |
rs771910977 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520583 | CTGACAGAAAGTCAG[C/T]CCTGTTACTCTTTGC | 89910 |
rs771913236 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481538 | TTTAAAAAACCATTG[G/T]CATTGTAGTTACTAC | 89910 |
rs771930135 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480652 | GAGACCCTGCCTTAA[-/A]AAAAAAAAAAAAGAC | 89910 |
rs771955083 | in-del | -/GA | 1.64727e-05 | 0.00286986 | frameshift-variant, intron-variant | UBE3B | GRCh38.p7 | 12:109530017 | ATGTTCTCAACTCCT[-/GA]ACTGCAGCGTCTCAT | 89910 |
rs771969794 | snp | C/T | 0.000115303 | 0.00759199 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521234 | TGACCTCGGGGTGGA[C/T]GAAGCAGGGATTGAT | 89910 |
rs772019008 | snp | A/G | 1.67576e-05 | 0.00289457 | intron-variant | UBE3B | GRCh38.p7 | 12:109507759 | ACTGCTGTGGGACTG[A/G]ATTCCTTTCCTAGAA | 89910 |
rs772022748 | snp | G/T | 1.65507e-05 | 0.00287664 | intron-variant | UBE3B | GRCh38.p7 | 12:109521374 | GCCAGATTCAAGAAG[G/T]GAAGAGCTGGGCTTG | 89910 |
rs772063272 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541617 | TCCATTGGCTCCTAT[A/G]TTGGTTTCCCATGGC | 89910 |
rs772068203 | snp | C/T | 1.82174e-05 | 0.00301801 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534542 | TGGCATCAGCCTGGG[C/T]TCCCAAACTAGGCCC | 89910 |
rs772074081 | snp | A/C | 1.65375e-05 | 0.0028755 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509679 | CCTCTTTCCTGAATT[A/C]TTTTGTGTTTAAGAT | 89910 |
rs772082369 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532859 | TCTCTTGCACAGGGT[-/C]CCCCCGGGGCCCCAG | 89910 |
rs772113376 | snp | G/T | 3.30322e-05 | 0.00406387 | intron-variant | UBE3B | GRCh38.p7 | 12:109523967 | ACAGCTCTGCTTCTC[G/T]GCTCTCCCAGGGAAT | 89910 |
rs772118009 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531700 | CACATCCCCACAGGT[C/T]TCCGGGGATTTAGGA | 89910 |
rs772157158 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540680 | GTGTCCTTGGCCTTC[A/G]GACCACGGGCATGTG | 89910 |
rs772185960 | in-del | -/TTTTGT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506337 | ACAGACCCAAATCTG[-/TTTTGT]TTTTGTTTTTGTTTT | 89910 |
rs772223833 | snp | C/T | 1.77625e-05 | 0.00298009 | intron-variant | UBE3B | GRCh38.p7 | 12:109511188 | ATTCTCCCAAACCCA[C/T]GTCTTTCTTCTCAAG | 89910 |
rs772274562 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109498916 | CTGCATCCTCTACCT[C/T]CTGGGCTTAGGTGAT | 89910 |
rs772277846 | snp | C/T | 3.30344e-05 | 0.004064 | intron-variant | UBE3B | GRCh38.p7 | 12:109501347 | ATGGAACTGACAGAC[C/T]AGGTCTCCTCTGCTC | 89910 |
rs772278597 | snp | C/T | 3.54095e-05 | 0.00420755 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534746 | CGAGAAGCTGCGCTA[C/T]GCCATCAGCATGAAC | 89910 |
rs772329662 | snp | C/T | 1.6693e-05 | 0.00288898 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499696 | AGACAGATGGGTTCG[C/T]GAGTTTGCTCACCCA | 89910 |
rs772339726 | snp | C/G | 2.13673e-05 | 0.00326851 | intron-variant | UBE3B | GRCh38.p7 | 12:109486617 | AAGCAAAACCAGAAA[C/G]AGTACGTATGTCATT | 89910 |
rs772468185 | snp | A/C/G | 0.000296864 | 0.0121803 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516842 | CAGCTCTGCCTCCCC[A/C/G]CATGTCACTCACATC | 89910 |
rs772517838 | snp | A/C | 1.65666e-05 | 0.00287802 | intron-variant | UBE3B | GRCh38.p7 | 12:109533563 | CGGACGATCAGGTAC[A/C]CCCACGGGGTGGGTG | 89910 |
rs772522646 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | UBE3B | GRCh38.p7 | 12:109503209 | CGCAGTCCCCAGGGC[A/G]TCTTCTTCACCTCTC | 89910 |
rs772531767 | snp | C/T | 1.67279e-05 | 0.002892 | intron-variant | UBE3B | GRCh38.p7 | 12:109533598 | AGAGCCTTGACTTCC[C/T]TCTTGGTGGTTGTCT | 89910 |
rs772582055 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495568 | TATAGAGGTGTGGAG[C/T]AGGAAATCAGGGGTC | 89910 |
rs772589870 | snp | A/C | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536654 | TTTTGTAGCTAACTT[A/C]TGGATTGAGATGTGA | 89910 |
rs772602095 | snp | C/T | 4.94181e-05 | 0.00497057 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497872 | GCCGTTCCTCATCCA[C/T]ATCATGTCTGTGCCT | 89910 |
rs772631499 | snp | A/T | 3.45191e-05 | 0.00415432 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521532 | TTGTGGGGAAGATGC[A/T]GGGGAAGGCTGTGTA | 89910 |
rs772641598 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533385 | AACAGACAGAGCAAA[C/T]ACGTGCTACACAGCT | 89910 |
rs772670524 | snp | A/G | 4.94311e-05 | 0.00497123 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507622 | TATCTGTGAGCTCGG[A/G]CCCCACGGAGGGTTA | 89910 |
rs772670592 | snp | A/C | 1.65441e-05 | 0.00287607 | intron-variant | UBE3B | GRCh38.p7 | 12:109497970 | CCCAATTGTGTTTTT[A/C]TTTTCTTCTTAAACA | 89910 |
rs772714100 | snp | G/T | 1.64817e-05 | 0.00287064 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486541 | AGATCAAGAACATTT[G/T]GTGGTACTGCTGTGA | 89910 |
rs772741332 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504003 | GAAAGAGAGAGCCAA[A/G]TTCTTCGTTCTCAAG | 89910 |
rs772779323 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523840 | ATGGGGAGATACTGC[C/G]CTCCGGATTGGAAAC | 89910 |
rs772794700 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491586 | CTTAGTTTGGAGATG[G/T]CAGGTACTGAAGAAG | 89910 |
rs772809947 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493171 | TCTAGGTACAAACAG[G/T]TTTTCCCAGAAGCCT | 89910 |
rs772832344 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510534 | GCACTCAGCTCTCAT[G/T]TTCTAGGGCAGAGAG | 89910 |
rs772905395 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505701 | CCTTGAAAATGTGAG[G/T]TCTAAGCTCTAGGCA | 89910 |
rs772912009 | snp | C/T | 0.00014794 | 0.00859931 | intron-variant | UBE3B | GRCh38.p7 | 12:109533731 | AGGAGAACCAGCCAG[C/T]CCCAGAGAGACTGCC | 89910 |
rs772971664 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481625 | TGGATTTTTTTCTTC[C/T]GCTTCTGCCAGAAAA | 89910 |
rs772988554 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524038 | CTGCTTGGGCACCAC[C/T]ACAGCGTCTTCTATA | 89910 |
rs773005902 | snp | C/T | 4.94173e-05 | 0.00497053 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109529965 | AGCTGCCCTCATTAG[C/T]GGATTCCGTTCCATT | 89910 |
rs773020501 | in-del | -/GTTG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515367 | TATTACTGTTTTTTT[-/GTTG]TTGTTGTTGTTGTTT | 89910 |
rs773041616 | snp | A/G | 3.30409e-05 | 0.0040644 | intron-variant | UBE3B | GRCh38.p7 | 12:109524392 | AAACCTCTTAAGCAC[A/G]TAGTGCTCCATGGCC | 89910 |
rs773052415 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540692 | TTCAGACCACGGGCA[C/T]GTGAAAGAGAAGCTA | 89910 |
rs773061391 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511432 | GCACAAGGAAACGGT[C/G]GTTGCTATTACTTTG | 89910 |
rs773075131 | snp | C/T | 0.000511902 | 0.0159903 | intron-variant | UBE3B | GRCh38.p7 | 12:109518006 | GGATGTTTCTGACAT[C/T]CTTCAAGGTAGGCAT | 89910 |
rs773083125 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541624 | GCTCCTATATTGGTT[C/T]CCCATGGCTGCTGCA | 89910 |
rs773111165 | snp | A/T | 1.65181e-05 | 0.00287381 | intron-variant | UBE3B | GRCh38.p7 | 12:109490027 | ACTCCTGCCCCCCAG[A/T]GTGCAACTTCTCCAC | 89910 |
rs773146357 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497995 | TAAACATTAGAAAGT[A/G]AAATGGCTTCTCTGC | 89910 |
rs773175903 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539758 | TTAACAGGACATCCC[A/G]GGGATCCTCTGCTGG | 89910 |
rs773198609 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517437 | ATACGGTGACTCCAT[A/G]TAAATTAGAGATAGG | 89910 |
rs773223999 | in-del | -/A/AAC | 0.172336 | 0.23763 | splice-donor-variant | UBE3B | GRCh38.p7 | 12:109486577 | CAAGCAGCTCAAGGT[-/A/AAC]AACAAAAAAAAAAAA | 89910 |
rs773302539 | snp | C/T | 1.73168e-05 | 0.00294246 | intron-variant | UBE3B | GRCh38.p7 | 12:109521416 | GCACTTGACCTCTGC[C/T]TCTCCCCGTCTTTTT | 89910 |
rs773313003 | snp | C/T | 3.2981e-05 | 0.00406071 | intron-variant | UBE3B | GRCh38.p7 | 12:109497779 | TGTTCTGGATGCACA[C/T]GGAGACCTGTCTGAA | 89910 |
rs773314063 | in-del | -/T | 3.29641e-05 | 0.00405968 | intron-variant | UBE3B | GRCh38.p7 | 12:109489888 | ATTATGGCAAGAGAC[-/T]TTTTTTGTTCTCACT | 89910 |
rs773339219 | snp | C/T | 1.80912e-05 | 0.00300754 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534560 | CCAAACTAGGCCCTT[C/T]CCAATTCAAGGCCAC | 89910 |
rs773343082 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109498983 | AGCGCACACTACCAC[A/G]GCCGACTAATTTTTG | 89910 |
rs773351206 | snp | A/G | 1.70191e-05 | 0.00291706 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483705 | AGTCGACTGCAGAGA[A/G]ATATCAGGTAAGGGC | 89910 |
rs773359496 | snp | C/T | 1.6966e-05 | 0.00291251 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509731 | TAAGAGAAAAGGTGT[C/T]TGCTGTTGTTTGGTT | 89910 |
rs773398244 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109487676 | CAACAGATTGCTCTT[C/T]GAGGAGAAGCTCTTC | 89910 |
rs773418865 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488627 | TCACGATGCTTGTCA[C/T]CTTCACAGACACTTC | 89910 |
rs773419349 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477435 | TTGTGCGCCTAGGGG[A/C]CAGTTTTCTTTCCAG | 89910 |
rs773451092 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488419 | TTAACTCCTGGAGTG[G/T]TCATTGCCCAAGAGA | 89910 |
rs773457514 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513439 | TTGCAAAGCTGGCTT[A/G]TAAGAACAAAATAAA | 89910 |
rs773470198 | in-del | -/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528724 | CTGGACATGGTGGCA[-/G]GCGCTGTAATGTCAG | 89910 |
rs773471114 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520619 | ACCTTCTGCAGCTCC[C/G]ATTACCTTCAGGATG | 89910 |
rs773482730 | snp | G/T | 1.73054e-05 | 0.00294149 | intron-variant | UBE3B | GRCh38.p7 | 12:109509554 | TTTTTCTCTTCGCCT[G/T]TTTTCAGTGTGGAAT | 89910 |
rs773528269 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507824 | GTAATTGCTAATGTG[A/G]TTACTGCAAACATTT | 89910 |
rs773540817 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506321 | ATAAATTTTTACTAG[A/G]ACAGACCCAAATCTG | 89910 |
rs773634908 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109492739 | TGATACCTGGTCTCA[-/A]AAAAAAAAAAAAAAG | 89910 |
rs773641603 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513116 | TCTCCACCTCGTCTT[C/T]GTTTGAAATAGGCTC | 89910 |
rs773652159 | snp | A/G | 6.59359e-05 | 0.00574139 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491105 | AAAGGCACTTTAACA[A/G]CAGCTTTTTCTCTAG | 89910 |
rs773663593 | snp | A/G | 4.96159e-05 | 0.00498051 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511231 | TAGCGTGCTCTTCCA[A/G]GAACTCGACAGGGAC | 89910 |
rs773680775 | snp | A/G | 1.65138e-05 | 0.00287343 | intron-variant | UBE3B | GRCh38.p7 | 12:109524402 | AGCACATAGTGCTCC[A/G]TGGCCCTAACACTTT | 89910 |
rs773738610 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478482 | TCCTATTCTTTAAAT[-/A]AAAATTAGATTATTG | 89910 |
rs773828131 | snp | C/T | 1.65143e-05 | 0.00287348 | intron-variant | UBE3B | GRCh38.p7 | 12:109502977 | CAGGGTGGGATTTGG[C/T]AGCTGGCTGAGCTGC | 89910 |
rs773839621 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537843 | CCACATAGCTGGGAC[C/T]ACAGGTGCCCGCCAC | 89910 |
rs773851994 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525377 | AAAGAATGCTGTCTC[A/G]CAGGATCGTTCTCTA | 89910 |
rs773867430 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109488652 | CACTTCAACGTGGAA[A/G]ATTCTTCGGGGAAAA | 89910 |
rs773916402 | snp | A/C/T | 3.37849e-05 | 0.00410991 | intron-variant | UBE3B | GRCh38.p7 | 12:109501559 | GGGAGCAGGCCCAAC[A/C/T]CTGTAGCTCCACTTG | 89910 |
rs773938235 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526282 | ATGGATGTTTGTGCT[A/G]GGCCCTCTCATCTCC | 89910 |
rs773968783 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522217 | AGCCAGCTGCTCACA[C/G]CAGGTGGATCGGAGC | 89910 |
rs773989312 | snp | C/T | 1.71349e-05 | 0.00292697 | intron-variant | UBE3B | GRCh38.p7 | 12:109483720 | GATATCAGGTAAGGG[C/T]TAGGATCTCCCTAGC | 89910 |
rs774025233 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502911 | AGTGAGTTGCCCCAC[-/T]GTCTGGCCTGGCTGT | 89910 |
rs774029712 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528675 | CCTAGTCAACATGGT[A/G]AAACTCCGTCTCTAC | 89910 |
rs774069161 | in-del | -/T | 1.75317e-05 | 0.00296067 | intron-variant | UBE3B | GRCh38.p7 | 12:109511191 | TCCCAAACCCATGTC[-/T]TTTCTTCTCAAGGGA | 89910 |
rs774102266 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491315 | TTAATCTTCAGTCTT[G/T]AATATTTCTTAATCT | 89910 |
rs774138409 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109514613 | TGCCAAAGATTTGGG[A/G]TCATAGGAAGTAGTT | 89910 |
rs774145584 | snp | A/G | 1.65162e-05 | 0.00287365 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511243 | CCAAGAACTCGACAG[A/G]GACAGAAAACGGGCA | 89910 |
rs774157395 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480410 | CCTAACATTTTGGGA[A/G]GCCAAGGCAGGAGGA | 89910 |
rs774162325 | in-del | -/C | 1.64955e-05 | 0.00287184 | intron-variant | UBE3B | GRCh38.p7 | 12:109490019 | GGTCTGTGACTCCTG[-/C]CCCCCAGTGTGCAAC | 89910 |
rs774184557 | snp | C/G | 5.11365e-05 | 0.00505625 | intron-variant | UBE3B | GRCh38.p7 | 12:109511321 | GAGTTGCACTCAGAG[C/G]TGGGCCCCGATGTGT | 89910 |
rs774201507 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523608 | GCCCCTGCCAATGCC[A/G]TGGCTGCCCTGAGAG | 89910 |
rs774203713 | snp | C/T | 6.65015e-05 | 0.00576596 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507735 | CGCGGCACCTCATCA[C/T]GTAGGTTGACTGCTG | 89910 |
rs774208483 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109481443 | TTTATTTTCAACATA[C/T]TCCCTTTAAACTGTG | 89910 |
rs774229226 | snp | A/G | 3.29837e-05 | 0.00406088 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483875 | GGAGAGAGATTGATG[A/G]CTTTTTTAAAGCAGA | 89910 |
rs774304507 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109539008 | TGGGAGGCTGAGGCG[C/G]GCAGATCCCCTGAGG | 89910 |
rs774310336 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485833 | CCACCAGTTGGAGAA[A/C]CCTTTAGTCTTTATG | 89910 |
rs774368115 | snp | C/T | 3.44424e-05 | 0.0041497 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521529 | AGTTTGTGGGGAAGA[C/T]GCTGGGGAAGGCTGT | 89910 |
rs774395024 | snp | C/T | 3.29511e-05 | 0.00405887 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498266 | TCCCATGACATGCTT[C/T]GTAAATTCATCATAT | 89910 |
rs774422074 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521212 | TCATCCGTGTGAAGT[C/T]TGTCAATGACCTCGG | 89910 |
rs774441855 | snp | C/G | 1.71593e-05 | 0.00292905 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509751 | GTTGTTTGGTTGATG[C/G]TGCACCCAGGGAGGC | 89910 |
rs774460468 | snp | G/T | 1.67144e-05 | 0.00289084 | intron-variant | UBE3B | GRCh38.p7 | 12:109486439 | ATGATCTCTATAACA[G/T]CCCATGACATTCCTC | 89910 |
rs774470180 | snp | G/T | 1.65072e-05 | 0.00287286 | intron-variant | UBE3B | GRCh38.p7 | 12:109526458 | GTCACCACTTGAAAA[G/T]ACTTCATTCTGGCTC | 89910 |
rs774495273 | snp | A/G | 1.71287e-05 | 0.00292644 | intron-variant | UBE3B | GRCh38.p7 | 12:109499821 | TATGGGTGAGTCCCA[A/G]ATGCAAATCACTGTC | 89910 |
rs774553326 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109529307 | CCCAGAGACCCTCTG[C/T]TTGGAACCATTGTAA | 89910 |
rs774583113 | snp | A/C | 1.6486e-05 | 0.00287102 | intron-variant | UBE3B | GRCh38.p7 | 12:109497782 | TCTGGATGCACACGG[A/C]GACCTGTCTGAATGA | 89910 |
rs774593011 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506740 | TGTTAGACTAAATTT[A/G]GCCTGAGGATGCCTC | 89910 |
rs774651376 | in-del | -/AG | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109537076 | ACCAGTCGCGAACTC[-/AG]GGGCTCAAGTGATCC | 89910 |
rs774659462 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519030 | GGCTATGCTTCTCTA[G/T]TAGGCTTCCAGATAT | 89910 |
rs774679982 | snp | A/G | 3.39219e-05 | 0.00411823 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477275 | CATGAAAAGTCGGAG[A/G]ACGCAGGAGTCTCCA | 89910 |
rs774684877 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109518141 | AAATAATCTCCACTT[C/T]TGCGCCCTCCTGTTC | 89910 |
rs774691514 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533622 | GTTGTCTGCTGTGCC[C/T]ACTGTGCAAGGCCCT | 89910 |
rs774735935 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505747 | TACAATTCTTGGCCT[C/T]CTTTAGAATTCCTTC | 89910 |
rs774779282 | snp | C/G | 1.78033e-05 | 0.00298351 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486035 | GAAGTTGTGTCGCAG[C/G]ATCCTGAGCAGCATG | 89910 |
rs774801610 | snp | A/T | 1.749e-05 | 0.00295714 | intron-variant | UBE3B | GRCh38.p7 | 12:109511331 | CAGAGCTGGGCCCCG[A/T]TGTGTCTTTCTATTC | 89910 |
rs774806358 | snp | C/G/T | 3.30236e-05 | 0.00406336 | intron-variant | UBE3B | GRCh38.p7 | 12:109502984 | GGATTTGGCAGCTGG[C/G/T]TGAGCTGCTGCTCAC | 89910 |
rs774829351 | snp | A/G | 1.6557e-05 | 0.00287719 | intron-variant | UBE3B | GRCh38.p7 | 12:109530677 | TTTTATTTATTACCT[A/G]TGCATGCATGCATGT | 89910 |
rs774882565 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant | UBE3B | GRCh38.p7 | 12:109533457 | CACTGACCCTGCTTT[A/G]TGTTGCAGTTCGTGA | 89910 |
rs774907684 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484120 | CTTTTGTTTTCTTGG[G/T]ACCTGTTTTGGAGGG | 89910 |
rs774966784 | snp | C/T | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536606 | ACACCTTGATGGCTC[C/T]TGATGGCTCTAAAAA | 89910 |
rs774988529 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512815 | AAGTGAAGGGCCTTA[C/T]GGCAATTACTTAATC | 89910 |
rs775000920 | snp | A/C | 3.39512e-05 | 0.00412001 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477280 | AAAGTCGGAGGACGC[A/C]GGAGTCTCCAAACCC | 89910 |
rs775038737 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541573 | AGTATTGGGTCAGAA[C/G]GTAACTCTCATTGCT | 89910 |
rs775074829 | in-del | -/AAG | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536490 | ATGTGGATTTTTGAC[-/AAG]AAGGAGGGGTAGTTT | 89910 |
rs775115131 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482772 | AGATAAAAACTTAGT[A/G]TATAATTTAGAGCTG | 89910 |
rs775158527 | in-del | -/AT | 1.73942e-05 | 0.00294903 | intron-variant | UBE3B | GRCh38.p7 | 12:109484017 | ATGTATAATACTTCC[-/AT]ATGTCAGATCTTTTA | 89910 |
rs775174414 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526083 | GTCCTACTCTACTCC[A/G]AAATGCCAACACATT | 89910 |
rs775203882 | snp | C/T | 1.65154e-05 | 0.00287358 | intron-variant | UBE3B | GRCh38.p7 | 12:109516753 | TTCTGATCCCGCCTT[C/T]GTTCATTTTAGAGAG | 89910 |
rs775226332 | snp | C/T | 1.64939e-05 | 0.0028717 | intron-variant | UBE3B | GRCh38.p7 | 12:109533415 | TGCAAGGGCCCGTCC[C/T]GGAAGAGCAGGAGCC | 89910 |
rs775234306 | in-del | -/ATGC | 1.65445e-05 | 0.00287611 | intron-variant | UBE3B | GRCh38.p7 | 12:109530677 | TTTTATTTATTACCT[-/ATGC]ATGCATGCATGTATT | 89910 |
rs775266234 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109536359 | TTCGTGCATACATGC[A/G]GGGACCCCAGACTGT | 89910 |
rs775298288 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542541 | CAGCATGTGGCCTTA[C/T]TTGGAAATAGGGTTG | 89910 |
rs775331033 | snp | G/T | 3.4239e-05 | 0.00413743 | intron-variant | UBE3B | GRCh38.p7 | 12:109484007 | AATAGCAAACATGTA[G/T]AATACTTCCATATGT | 89910 |
rs775343889 | snp | A/T | 1.7364e-05 | 0.00294647 | stop-gained, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499665 | GGCTCCCTCAGCCCC[A/T]GAGTGTTAGAGGAGG | 89910 |
rs775372931 | snp | C/T | 1.68295e-05 | 0.00290077 | intron-variant | UBE3B | GRCh38.p7 | 12:109507769 | GACTGAATTCCTTTC[C/T]TAGAATATGGAGAGA | 89910 |
rs775377841 | snp | C/T | 1.82111e-05 | 0.00301749 | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534545 | CATCAGCCTGGGCTC[C/T]CAAACTAGGCCCTTC | 89910 |
rs775389125 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109509392 | AGCTCTACATGCATT[A/G]GGTATTTGTCCTAAG | 89910 |
rs775413330 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480322 | CATTTAGTCCTCATT[A/G]TCAACCTCTAAGCCA | 89910 |
rs775428092 | snp | C/T | 1.65408e-05 | 0.00287578 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509680 | CTCTTTCCTGAATTC[C/T]TTTGTGTTTAAGATG | 89910 |
rs775430715 | snp | A/G | 1.68655e-05 | 0.00290387 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534636 | CGGGGCTTCTTCACC[A/G]TCCGCAAGCGGGAGC | 89910 |
rs775498000 | snp | A/G | 1.72151e-05 | 0.00293381 | intron-variant | UBE3B | GRCh38.p7 | 12:109499827 | TGAGTCCCAGATGCA[A/G]ATCACTGTCTTTCCT | 89910 |
rs775498457 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485887 | GAAGGAACTGCATGT[A/G]ATTATGTGTGAATCA | 89910 |
rs775500082 | snp | G/T | 8.2067e-05 | 0.00640521 | intron-variant | UBE3B | GRCh38.p7 | 12:109510469 | CGAAAGTGAGCTCCA[G/T]GGGTGAGGAGGGCTC | 89910 |
rs775549215 | snp | G/T | 1.65075e-05 | 0.00287289 | intron-variant | UBE3B | GRCh38.p7 | 12:109501359 | GACCAGGTCTCCTCT[G/T]CTCTCTCCTAGCCTT | 89910 |
rs775567447 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533034 | TGCAGTGGGTGCCAC[C/T]AGCCTCCGCCTCGCC | 89910 |
rs775569091 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520687 | TGATTGGGAAGGCAG[C/T]GGGAGATGAGGGGTG | 89910 |
rs775578305 | snp | A/G | 1.77263e-05 | 0.00297705 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534747 | GAGAAGCTGCGCTAC[A/G]CCATCAGCATGAACA | 89910 |
rs775634353 | snp | C/T | 0.000140855 | 0.00839093 | synonymous-codon, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490492 | TCCTTCTCCCTAGTG[C/T]TGTGATGGGCTGTTT | 89910 |
rs775651878 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510188 | TGCAGACACTTAGCA[C/T]TTACCCAGGGTGCCT | 89910 |
rs775675047 | snp | C/T | 1.65034e-05 | 0.00287253 | intron-variant | UBE3B | GRCh38.p7 | 12:109503210 | GCAGTCCCCAGGGCA[C/T]CTTCTTCACCTCTCA | 89910 |
rs775755821 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485285 | CTTCACATTGTGCCA[A/G]CCCTCTCTAGGCACT | 89910 |
rs775770252 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483734 | GCTAGGATCTCCCTA[G/T]CACATGATTCTCTGG | 89910 |
rs775807411 | in-del | -/A | 1.66454e-05 | 0.00288486 | frameshift-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511298 | CATGTCATCCCTCAC[-/A]AAAACGTGAGTTGCA | 89910 |
rs775823980 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527883 | GCAGTGATGTTTACC[A/G]TCCTCAGATGGGTGA | 89910 |
rs775842844 | snp | G/T | 1.73501e-05 | 0.00294529 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521544 | TGCTGGGGAAGGCTG[G/T]GTATGAGGTAGGAAC | 89910 |
rs775845272 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109529973 | TCATTAGCGGATTCC[A/G]TTCCATTATCAAACC | 89910 |
rs775879123 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517321 | GAGTTATGTAGAGAA[A/G]TACTTTTATCACAGA | 89910 |
rs775881980 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109530049 | CTCTGGCGACAATGC[C/T]GAGATTGATCTGGAA | 89910 |
rs775891742 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE3B | GRCh38.p7 | 12:109534323 | GTTAACCAGTAATTC[A/G]CTGTGAACCGGAAGG | 89910 |
rs775915235 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475560 | GTATCTCAGAGATGC[A/G]GAGGGGTGGCTGATC | 89910 |
rs775953709 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497876 | TTCCTCATCCACATC[A/G]TGTCTGTGCCTGCTC | 89910 |
rs775958934 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503118 | GCAGAAGTCCAGAAG[A/G]TTTGCAACATCTGTG | 89910 |
rs775972278 | in-del | -/AAGG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538213 | AGCCTGTTAGCAGAC[-/AAGG]AAGGCACTGCTGAAA | 89910 |
rs775981553 | snp | G/T | 1.66363e-05 | 0.00288407 | stop-gained, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483612 | GCCCGTCAGGCACGA[G/T]AAGAAAGGCTTGTGC | 89910 |
rs776054210 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109494122 | AGTGAGCCACCACAC[C/T]TGGCTTTTCTCCATT | 89910 |
rs776061254 | in-del | -/TG | 1.64789e-05 | 0.0028704 | intron-variant | UBE3B | GRCh38.p7 | 12:109488554 | GTGTCTTAATCTTGC[-/TG]TGTTTATTGTTTCCA | 89910 |
rs776070821 | snp | C/T | 3.30721e-05 | 0.00406632 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516860 | TGTCACTCACATCAC[C/T]ATCCGCCGGTCCAGG | 89910 |
rs776125794 | snp | A/C | 1.65119e-05 | 0.00287327 | intron-variant | UBE3B | GRCh38.p7 | 12:109503217 | CCAGGGCATCTTCTT[A/C]ACCTCTCACATTTGG | 89910 |
rs776146876 | snp | A/G | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535654 | GTTATCTAATGAGGA[A/G]CAAACACTAACCTAA | 89910 |
rs776177338 | in-del | -/CTAGTTTCCACTTTTCTTCCTTTTGCATTACAGGA | 1.67125e-05 | 0.00289067 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486561 | ACTGCTGTGATTTTC[lengthTooLong]TCAAGCAGCTCAAGG | 89910 |
rs776193459 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505550 | ATTTTTGAATTGTGA[A/G]AGTTCCACATTCTTG | 89910 |
rs776228289 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520831 | TGTATCTTGTCCCGG[G/T]TTCTTTCATCCTTTG | 89910 |
rs776234508 | snp | C/G | 1.69703e-05 | 0.00291288 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483696 | CTCTGTCGGAGTCGA[C/G]TGCAGAGAGATATCA | 89910 |
rs776246224 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493374 | TCTAGGAGCACCTCA[A/C]CTTTCTTACCTGTCC | 89910 |
rs776253847 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109499077 | ATCCACACGCCTCAG[C/G]CTGCGAGATTACAGA | 89910 |
rs776316953 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525117 | TAGACTCGCGCTTGG[G/T]CACCTCAGAACCCCC | 89910 |
rs776374559 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512459 | AGCAAGCATGGCTCA[C/T]GTCCCTGGTGAGTGG | 89910 |
rs776377131 | snp | A/G | 7.06739e-05 | 0.00594407 | intron-variant | UBE3B | GRCh38.p7 | 12:109521554 | GGCTGTGTATGAGGT[A/G]GGAACGTTAAGAAAC | 89910 |
rs776407171 | snp | A/G | 0.000164883 | 0.00907824 | intron-variant | UBE3B | GRCh38.p7 | 12:109497954 | GAGTTCCCCGTGAAA[A/G]CCCAATTGTGTTTTT | 89910 |
rs776429830 | snp | C/T | 3.37177e-05 | 0.00410582 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534645 | TTCACCATCCGCAAG[C/T]GGGAGCCAGGCGGCC | 89910 |
rs776447942 | snp | G/T | 2.04794e-05 | 0.00319989 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510390 | CCAGTCTGTCCACGG[G/T]TGGCTTATGGTGCTG | 89910 |
rs776453882 | snp | G/T | 1.65963e-05 | 0.0028806 | intron-variant | UBE3B | GRCh38.p7 | 12:109533575 | TACCCCCACGGGGTG[G/T]GTGGGGAAGAGCCTT | 89910 |
rs776473657 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109529953 | AAAAAACCAAACAGC[C/T]GCCCTCATTAGCGGA | 89910 |
rs776482506 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525488 | AAAACCCACTGGTGC[C/T]ACCTGAGATGCTGAC | 89910 |
rs776520335 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520655 | TAAATTCCTCAGCAT[C/G]ACTTGCAGGCACTTC | 89910 |
rs776529477 | snp | A/T | 1.68165e-05 | 0.00289965 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499688 | AGAGGAGGAGACAGA[A/T]GGGTTCGTGAGTTTG | 89910 |
rs776536072 | snp | A/G | 1.64944e-05 | 0.00287175 | intron-variant | UBE3B | GRCh38.p7 | 12:109526442 | CAATTAGGTTTTTAA[A/G]GTCACCACTTGAAAA | 89910 |
rs776546853 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489390 | GAAGTGGTGTGTGAG[C/G]TGAGAGCTGCAGAGG | 89910 |
rs776578322 | snp | A/G | 3.29484e-05 | 0.00405871 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109489938 | AAGTCTTCGACCAGC[A/G]ATGAACCACATTTGT | 89910 |
rs776582499 | snp | A/T | 1.65883e-05 | 0.00287991 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499772 | CCTGACCCACTGGCA[A/T]CCTGTCCTTGGCTGG | 89910 |
rs776589075 | snp | A/G | 1.64933e-05 | 0.00287165 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516773 | ATTTTAGAGAGTTCT[A/G]CTGTTTCGAACCATG | 89910 |
rs776667981 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519555 | ACGCATCTACTAATG[C/T]GTGTGAAGGCTGGGG | 89910 |
rs776694775 | snp | C/T | 1.69991e-05 | 0.00291535 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477287 | GAGGACGCAGGAGTC[C/T]CCAAACCCGGACTGA | 89910 |
rs776694880 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488501 | GCCCATAGAGCAGTT[A/G]TAAAGTGAACACTTC | 89910 |
rs776701584 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491094 | CTTGTCTATCCAAAG[A/G]CACTTTAACAGCAGC | 89910 |
rs776702371 | snp | A/G | 0.000231462 | 0.0107554 | intron-variant | UBE3B | GRCh38.p7 | 12:109530508 | TCCATAAGTGCCCAC[A/G]CTAGCACATTGCTGA | 89910 |
rs776705173 | snp | A/G | 6.59968e-05 | 0.00574404 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109530070 | TGATCTGGAAGATTT[A/G]AAGTAAGAGGCGGGT | 89910 |
rs776777512 | in-del | -/A | 2.31629e-05 | 0.00340307 | intron-variant | UBE3B | GRCh38.p7 | 12:109533655 | TCTAGTCCATATCTC[-/A]GCAAGGCAGGCAGCT | 89910 |
rs776782001 | snp | A/G | 1.64871e-05 | 0.00287111 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483889 | GACTTTTTTAAAGCA[A/G]ATGACCCTGAGTCCA | 89910 |
rs776802245 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538841 | GCAAAGTGCCTTTCA[G/T]CCAGAAGGATCCAGC | 89910 |
rs776824588 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478193 | GAGGGTGTGAATACG[-/T]TTTAGTACCGTGCCT | 89910 |
rs776878584 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | UBE3B | GRCh38.p7 | 12:109488530 | TCACTGTCTGGAATC[A/G]GAAGACGTGTGTCTT | 89910 |
rs776895286 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489645 | GAAAAGGTGCTACAG[G/T]CGCTCAGAGGCCAGA | 89910 |
rs776908594 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | UBE3B | GRCh38.p7 | 12:109497768 | GGTTGTGCTTTTGTT[C/T]TGGATGCACACGGAG | 89910 |
rs776938874 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538169 | ACAGAGTTTGAGAAG[C/T]GCTGGCCTCCACTCT | 89910 |
rs776947244 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496326 | TTTTTGGCTATTATA[A/G]ATAGTGCTGCTGTGA | 89910 |
rs776951480 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484177 | TTTCACATTGACCAT[C/T]ATAAGCACAAGTTGA | 89910 |
rs776965405 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109509268 | TTTTATTTTTATTTT[A/G]TTTTACTTTAAGTTC | 89910 |
rs776979160 | snp | A/G | 1.6495e-05 | 0.0028718 | intron-variant | UBE3B | GRCh38.p7 | 12:109521144 | GTAATTCTGCTCTTG[A/G]CAGGACGGCTACGAG | 89910 |
rs776995115 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527758 | AGCATGGTGAGTCCT[G/T]CCCCTGCCTGCCATG | 89910 |
rs777000643 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485020 | CCTCAGCATCCCAAA[C/G]TGCTGGGATTACAGG | 89910 |
rs777032511 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521235 | GACCTCGGGGTGGAC[A/G]AAGCAGGGATTGATC | 89910 |
rs777094936 | snp | A/T | 1.64735e-05 | 0.00286993 | missense, intron-variant | UBE3B | GRCh38.p7 | 12:109530609 | TCATCTGGCTCTGGG[A/T]TATTCTGGCCTCCGA | 89910 |
rs777101546 | snp | A/T | 3.29685e-05 | 0.00405995 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486549 | AACATTTTGTGGTAC[A/T]GCTGTGATTTTCTCA | 89910 |
rs777150314 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | UBE3B | GRCh38.p7 | 12:109521344 | TTAAGGGGAGCAACA[A/G]CAGGGCTGACAGCAG | 89910 |
rs777168095 | snp | A/C | 0.000329946 | 0.0128399 | intron-variant | UBE3B | GRCh38.p7 | 12:109501367 | CTCCTCTGCTCTCTC[A/C]TAGCCTTAACGAGTC | 89910 |
rs777189106 | snp | A/G | | | intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109508622 | AGGGACATGTAGGTG[A/G]CAGATTGGGTGAGGA | 89910 |
rs777247788 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486889 | CCTCTTGTTAAAAGT[A/G]CAGAAGCCGAACGTG | 89910 |
rs777312901 | snp | C/T | 1.65135e-05 | 0.00287341 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491147 | GTAAGAAACCATAGC[C/T]GAGGTGTTGGCATGT | 89910 |
rs777374306 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517887 | CTCCCTCGGTGCATC[A/G]TACCTTGTTTGTGTC | 89910 |
rs777392289 | in-del | -/TGT | 1.70009e-05 | 0.0029155 | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109509735 | AGAAAAGGTGTCTGC[-/TGT]TGTTTGGTTGATGCT | 89910 |
rs777400615 | snp | A/G | 1.65097e-05 | 0.00287308 | splice-acceptor-variant | UBE3B | GRCh38.p7 | 12:109483859 | TGCACTTTCTTTTCT[A/G]GGAGAGAGATTGATG | 89910 |
rs777440267 | snp | G/T | 0.000148274 | 0.008609 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501417 | CAGCTGCAGTTCTTG[G/T]GGGGGGTGCCTCTGA | 89910 |
rs777459573 | snp | C/G | 1.66341e-05 | 0.00288388 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483981 | CAAAGAGGATAATGA[C/G]GTAAAACGATAATAG | 89910 |
rs777470103 | snp | A/G | 1.64963e-05 | 0.00287192 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498349 | CCATACGCTTTGTCT[A/G]ATGGGTAAGTATCCG | 89910 |
rs777489921 | in-del | -/C | 1.64773e-05 | 0.00287026 | frameshift-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524083 | TGCCTTCTCTGGACT[-/C]CCGAGTTCTATAAAA | 89910 |
rs777503022 | snp | A/G | 1.85989e-05 | 0.00304945 | intron-variant | UBE3B | GRCh38.p7 | 12:109511181 | TCTTTTAATTCTCCC[A/G]AACCCATGTCTTTCT | 89910 |
rs777546046 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537370 | CAGGTGTTTGCCCCG[C/T]CTTGGTGCTTCTGTC | 89910 |
rs777572269 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517831 | CCCCACCAGCAGATG[A/G]CTTCTGGCAGCAGCT | 89910 |
rs777574524 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523017 | TGAATGTCATGCCAT[C/T]TCCCAGGCCTCGCCT | 89910 |
rs777631147 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506597 | CTCAGATGATCCACC[C/T]GCCTCAGCCTCCCAG | 89910 |
rs777653211 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482456 | TTTCAGAGTTATTTC[A/T]CTTAGGATAGATGGC | 89910 |
rs777654452 | in-del | -/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480189 | GCCTCTGCTGAAGAG[-/T]TTTTTTTTTTTTTTT | 89910 |
rs777686271 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109507376 | CATAGTCAGCACCCA[C/T]TGACTACTGGCTCTT | 89910 |
rs777734911 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109543370 | GGGAGTGGCTCGGCA[C/G]GGGGTCAGCGGCTGG | 89910 |
rs777742245 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525853 | AAAACGCAAGCTGCC[C/T]GTAATGCCAGTGCCC | 89910 |
rs777787383 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502519 | CTCTGTCTCATAGCT[A/G]GCAGTAAGCGTGGGC | 89910 |
rs777847492 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541222 | CTGCAGGCAGCAGGG[C/G]CTGTAGACACAGCAG | 89910 |
rs777889874 | snp | A/G | | | splice-donor-variant, intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478110 | GCTGTGTGACCTTGG[A/G]TGAGTTCCCTCACCT | 89910 |
rs777925635 | snp | C/T | 1.64942e-05 | 0.00287173 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491057 | CAGATATTGTTAACC[C/T]GTGGCCTGGCAAGAC | 89910 |
rs777958067 | snp | A/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516811 | AGGAGAAGGAGAAAC[A/T]GGGGCTGGTGGAAAC | 89910 |
rs777969427 | snp | C/T | 1.64857e-05 | 0.00287099 | intron-variant | UBE3B | GRCh38.p7 | 12:109533442 | AGCCTGCCCCGTCCC[C/T]ACTGACCCTGCTTTG | 89910 |
rs777984456 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478365 | TGATAAATAACTGTT[C/T]TGGATATACATGGAT | 89910 |
rs778021178 | snp | G/T | 1.65272e-05 | 0.0028746 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109533544 | ATCCGCTGCGTGGAG[G/T]TGTCGGACGATCAGG | 89910 |
rs778050946 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531746 | AATTCCAGAAGTTGA[C/T]TCTGGGAGAATCAGT | 89910 |
rs778069857 | snp | G/T | | | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521465 | GGGGATGAGAGGCTG[G/T]ACCCCTCACCCACAT | 89910 |
rs778071803 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109489330 | ATGAGAGTGTCCAGT[A/C]GGGTGGGGAGGCCTT | 89910 |
rs778076862 | snp | C/G | 1.648e-05 | 0.0028705 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109490002 | TTTTATTCTGTGCTG[C/G]AGGTCTGTGACTCCT | 89910 |
rs778080265 | snp | A/G | 3.8997e-05 | 0.00441554 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499636 | CTCTCTCTGTAGGCA[A/G]CCTCCTACACTTGGG | 89910 |
rs778119408 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522939 | GTTTTCCTTTAAACA[C/T]GTTGCTGTGATGACA | 89910 |
rs778142511 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109530886 | GCAGGGACAGGCCCC[C/T]TGCACAGGTGGGCAT | 89910 |
rs778155158 | snp | A/G | 3.44151e-05 | 0.00414806 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109534597 | TGCCTTCAGGACACC[A/G]GGGACACTCTGGGCA | 89910 |
rs778170508 | in-del | -/C | 1.80579e-05 | 0.00300476 | intron-variant | UBE3B | GRCh38.p7 | 12:109483507 | CAACAATCTACAACA[-/C]CCACTTGCCCATTTT | 89910 |
rs778216612 | in-del | -/AG | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502436 | AATGCATAATTTGAC[-/AG]AGTTACCTGCCTGTG | 89910 |
rs778237173 | snp | C/T | 1.65198e-05 | 0.00287395 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524485 | GACGCTGTCTTACGA[C/T]GAGGACGTCATGGGT | 89910 |
rs778260208 | in-del | -/A/AA | 0.35266 | 0.249787 | intron-variant | UBE3B | GRCh38.p7 | 12:109486580 | GCAGCTCAAGGTAAC[-/A/AA]AAAAAAAAAAAAAAA | 89910 |
rs778266028 | snp | C/G | | | missense, intron-variant, utr-variant-5-prime | UBE3B | GRCh38.p7 | 12:109490508 | TGTGATGGGCTGTTT[C/G]CTGATTTGGTTTCAT | 89910 |
rs778266973 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497643 | ATGGCATCAGCAACT[A/G]GACCATCACTGACTT | 89910 |
rs778292141 | snp | C/T | 4.94238e-05 | 0.00497086 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109526366 | CCCCCAGCTTGTTTG[C/T]CATGAACTGATTCCT | 89910 |
rs778309991 | snp | A/C/G | 1.65026e-05 | 0.00287246 | intron-variant | UBE3B | GRCh38.p7 | 12:109530528 | CACATTGCTGAGCCC[A/C/G]GGTCTGTATTGCTTT | 89910 |
rs778323368 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510062 | TGAGAGTCCACCTCC[C/T]GAAGTGTCTCCAATT | 89910 |
rs778414717 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109496226 | TCAGAGTTCATCCAC[A/G]TTGTAGCATGGATCA | 89910 |
rs778420746 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533143 | CCACAGGAGACCTGC[C/G]TCTCGGGGACGCCTC | 89910 |
rs778421140 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488968 | TTACATTCACTTAAG[C/T]CTTGTCATTTTACTT | 89910 |
rs778443017 | snp | A/G | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509660 | GAAGAGCTGGTCACT[A/G]TCTCCTCTTTCCTGA | 89910 |
rs778460147 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109538759 | CTTAGGCAAGATCGG[A/G]GGAAAGTCACATTCC | 89910 |
rs778467025 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109526382 | CATGAACTGATTCCT[A/G]GAGGGAAGACCATTC | 89910 |
rs778484611 | snp | C/T | 0.000149354 | 0.0086403 | intron-variant | UBE3B | GRCh38.p7 | 12:109516717 | GTGTTTTTATGGAAT[C/T]GTCAGTTTGCTGACC | 89910 |
rs778493484 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109499735 | GCTACTGTCGGAAGT[A/G]TGTGTCTCAGAAGAA | 89910 |
rs778507041 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109505495 | AGTATATTTGTGATC[C/T]CCACAGTGTTAACTG | 89910 |
rs778517210 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527633 | ATTGAAATACACCGG[C/T]CTTGCTCCTTGGCCA | 89910 |
rs778527208 | snp | C/T | 1.72249e-05 | 0.00293465 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521485 | CTCACCCACATCCTA[C/T]ATCCATGAGAATTAC | 89910 |
rs778580960 | snp | A/C | | | downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109543761 | TCACTTGAACCCGGG[A/C]GGCAGAAGGTTGCAG | 89910 |
rs778589223 | snp | A/G | 1.68801e-05 | 0.00290512 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534688 | CCTCCACCTGCTTCA[A/G]CCTGCTCAAGCTGCC | 89910 |
rs778682295 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517803 | CCCCTGAAGTATGTG[A/G]CCAGATAGCCACCCC | 89910 |
rs778763429 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524605 | GCCCCAAGCTGAGGC[C/T]CTGTCTGGTCCCTTG | 89910 |
rs778823190 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109522748 | GGAATCAGGTGGCCC[-/A]TCTGAGCCCCTGCCC | 89910 |
rs778989368 | in-del | -/C | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478762 | CTCCAGCCTGGGCAA[-/C]AAAGTGAGACTCCGT | 89910 |
rs779006274 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109483211 | TTGAATTAGAGCTTT[A/C]TGGGTGGGACTGATT | 89910 |
rs779011155 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109524988 | TCTGTAGCAGCCTCC[G/T]CGCCCTTTGATTGTG | 89910 |
rs779041350 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541120 | CTCAGACCATGTTCC[A/G]GCGTGGTCCACCTGC | 89910 |
rs779079358 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537379 | GCCCCGCCTTGGTGC[C/T]TCTGTCCTGACCCTC | 89910 |
rs779094781 | snp | C/G | 1.65433e-05 | 0.002876 | intron-variant | UBE3B | GRCh38.p7 | 12:109516742 | CTGACCCTGTTTTCT[C/G]ATCCCGCCTTTGTTC | 89910 |
rs779100203 | snp | C/T | 1.65515e-05 | 0.00287671 | intron-variant | UBE3B | GRCh38.p7 | 12:109523957 | TGGCTGATGGACAGC[C/T]CTGCTTCTCTGCTCT | 89910 |
rs779103751 | snp | G/T | 1.64795e-05 | 0.00287045 | intron-variant | UBE3B | GRCh38.p7 | 12:109497939 | GTAAGCAGGCTCTGT[G/T]AGTTCCCCGTGAAAA | 89910 |
rs779127680 | snp | A/G | 6.11889e-05 | 0.00553089 | intron-variant | UBE3B | GRCh38.p7 | 12:109486612 | AAAAAAAGCAAAACC[A/G]GAAACAGTACGTATG | 89910 |
rs779146543 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512251 | TGACTCCCCCCATAA[C/T]CTGGGCGAGGTGGTT | 89910 |
rs779152969 | snp | A/G | 8.26781e-05 | 0.00642901 | intron-variant | UBE3B | GRCh38.p7 | 12:109498215 | GTTTCTGATTTAACG[A/G]TCTGCTATTCTTTGC | 89910 |
rs779153754 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524068 | AGCTCGGTGGATGAA[C/T]TGCCTTCTCTGGACT | 89910 |
rs779186103 | snp | A/C/T | 8.92071e-05 | 0.0066781 | intron-variant | UBE3B | GRCh38.p7 | 12:109533677 | CAGGCAGCTGGACCC[A/C/T]TCAGAGCCAAGTGAG | 89910 |
rs779197075 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531613 | TTTCCTCTCTCCTGG[G/T]TGGTCATTCTGAGGA | 89910 |
rs779212378 | snp | A/G | 3.30366e-05 | 0.00406413 | intron-variant | UBE3B | GRCh38.p7 | 12:109521129 | GCTTCCTAATGGGCT[A/G]TAATTCTGCTCTTGG | 89910 |
rs779213811 | in-del | -/AGGT | 3.34694e-05 | 0.00409067 | intron-variant | UBE3B | GRCh38.p7 | 12:109501542 | GTGAAGAGTGAGTGA[-/AGGT]CGGGAGCAGGCCCAA | 89910 |
rs779243190 | snp | A/G | 2.40654e-05 | 0.00346873 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510453 | CGAGGACCACTGGCT[A/G]CGAAAGTGAGCTCCA | 89910 |
rs779252278 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532375 | GAATAGGAATAGATC[G/T]TGTTAATACTCTTTT | 89910 |
rs779252299 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520525 | GTCTCTGCTCCCTGC[A/G]TTGATCCCTGCCATC | 89910 |
rs779272983 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512720 | CTTTAATACTTATGG[G/T]TGCTATTCTTTCCCC | 89910 |
rs779284427 | snp | A/T | 1.64947e-05 | 0.00287177 | intron-variant | UBE3B | GRCh38.p7 | 12:109529880 | GTTATCTCTTCCTTG[A/T]TGGCAACAGAATTAG | 89910 |
rs779284561 | snp | C/T | 1.70551e-05 | 0.00292015 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483582 | CAGACCTCGAGAGCA[C/T]GGTTCATCGATAGAG | 89910 |
rs779284917 | snp | C/T | 8.49885e-05 | 0.00651821 | intron-variant | UBE3B | GRCh38.p7 | 12:109490052 | CTCCACTCTCCAACA[C/T]CTGCACTTGGATTTT | 89910 |
rs779314990 | in-del | -/AAAG | 1.87661e-05 | 0.00306312 | intron-variant | UBE3B | GRCh38.p7 | 12:109486600 | AAAAAAAAAAAAAAA[-/AAAG]AAAGCAAAACCAGAA | 89910 |
rs779335516 | snp | C/T | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109516838 | AAACCAGCTCTGCCT[C/T]CCCGCATGTCACTCA | 89910 |
rs779401795 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109508786 | TTCAGATAGAGCTGT[A/G]TCTTAAATGGCTCAT | 89910 |
rs779402156 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109500746 | TGAAACCTGGGGATA[A/G]TTTTCACCCTCCCTT | 89910 |
rs779418221 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478274 | TAGCCCCCACAGGCA[A/G]TCTTGCACTCTCAAC | 89910 |
rs779435030 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109526177 | CCTTTTGTATTGATC[A/G]TGCAGGGTCTGCTTG | 89910 |
rs779453997 | snp | C/G | 1.72835e-05 | 0.00293964 | intron-variant | UBE3B | GRCh38.p7 | 12:109521414 | AGGCACTTGACCTCT[C/G]CCTCTCCCCGTCTTT | 89910 |
rs779474280 | snp | A/G | 0.000344448 | 0.0131189 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534723 | TACAGCAAGAAGAGC[A/G]TCCTCCGCGAGAAGC | 89910 |
rs779532572 | snp | G/T | 0.000592885 | 0.0172073 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507664 | GGAATGCCTGAACAA[G/T]GACACTGAAGAGTCC | 89910 |
rs779588646 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488076 | GCATTAATCCATTTA[C/T]TTCTCACAACAACCC | 89910 |
rs779620109 | snp | A/G | 1.64966e-05 | 0.00287194 | intron-variant | UBE3B | GRCh38.p7 | 12:109503204 | AGGTTCGCAGTCCCC[A/G]GGGCATCTTCTTCAC | 89910 |
rs779665594 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537621 | ACAGTGTAACCACCT[A/G]CCTCCCCAAAACACA | 89910 |
rs779725749 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109517575 | CGATGTCTGTGTTAT[C/T]CATGCCACAGCCTCC | 89910 |
rs779730305 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant | UBE3B | GRCh38.p7 | 12:109530013 | CCGAATGTTCTCAAC[C/T]CCTGAACTGCAGCGT | 89910 |
rs779736754 | snp | A/G | 4.95651e-05 | 0.00497796 | intron-variant | UBE3B | GRCh38.p7 | 12:109501327 | TGGCCCTGGCCCTGC[A/G]TCAGATGGAACTGAC | 89910 |
rs779790098 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109484611 | TGGCCAGGATAGTCT[C/T]GATCTCTTAGCCTTG | 89910 |
rs779854553 | snp | A/G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109543510 | ACCCTACCTGGAATC[A/G/T]ATCCTTTGTTTCTCT | 89910 |
rs779857014 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109497905 | TCTGGTGACTCATCT[C/T]AGCACAGTGACCCCT | 89910 |
rs779898052 | snp | A/G | 1.64928e-05 | 0.00287161 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109491120 | GCAGCTTTTTCTCTA[A/G]CGTTACGGTGAGTAA | 89910 |
rs779906381 | snp | A/G | 1.64969e-05 | 0.00287196 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109486478 | ACCTATAGGTGTGGT[A/G]TGTGTCCCTGGCTTG | 89910 |
rs779937701 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476445 | CATCTCTACCCAGGG[A/T]CAATGAGCTACTCAG | 89910 |
rs779945321 | snp | C/T | 5.11862e-05 | 0.00505871 | intron-variant | UBE3B | GRCh38.p7 | 12:109521393 | GAGCTGGGCTTGCTC[C/T]TTGCAAGGCACTTGA | 89910 |
rs779946643 | snp | C/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524086 | CCTTCTCTGGACTCC[C/G]AGTTCTATAAAAACC | 89910 |
rs780025464 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501783 | GCCTCCCAAGTATAA[C/T]AGCTGGGACTACAGG | 89910 |
rs780034708 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109504907 | GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC | 89910 |
rs780086334 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109482123 | TGCCTTTCAATAACA[C/T]GTAATTAATTTAATA | 89910 |
rs780111946 | snp | G/T | 1.73821e-05 | 0.00294801 | intron-variant | UBE3B | GRCh38.p7 | 12:109511193 | CCCAAACCCATGTCT[G/T]TCTTCTCAAGGGATC | 89910 |
rs780145283 | snp | G/T | | | utr-variant-3-prime, intron-variant | UBE3B | GRCh38.p7 | 12:109535286 | AAGTTTCTGCCTCCA[G/T]GCCGTCCACAGCGCC | 89910 |
rs780186260 | snp | A/T | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109524460 | ATGGGGACATCACTG[A/T]CCTGGGCCTGACGCT | 89910 |
rs780192987 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533841 | GCTGTTTTTAGTGGC[C/G]TCTGGCCTCACCAGG | 89910 |
rs780201047 | snp | C/G | 0.000133975 | 0.00818348 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109510362 | ACGCCAAGGGTGAGA[C/G]CTTGGAGCTGTTCCA | 89910 |
rs780208266 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109511074 | TGAATGAGTATGGTC[A/G]TGTTCCCATCAGACT | 89910 |
rs780218892 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495634 | TTTACCCACGTATTT[A/C]CTGACAGCAAGCCAG | 89910 |
rs780242339 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109523486 | GTATGCCTGGGGCCT[C/T]GTACCAGTGCCTGGC | 89910 |
rs780254875 | snp | A/G | 2.16856e-05 | 0.00329277 | intron-variant | UBE3B | GRCh38.p7 | 12:109486619 | GCAAAACCAGAAACA[A/G]TACGTATGTCATTTT | 89910 |
rs780259260 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109498545 | AAAATATTCCAGCCT[A/G]GCAAACTAGTTAAGT | 89910 |
rs780297349 | snp | G/T | 0.00014844 | 0.00861383 | intron-variant | UBE3B | GRCh38.p7 | 12:109524427 | CACTTTCCCCTTCTC[G/T]GTTACATTAGCGCTA | 89910 |
rs780309495 | snp | C/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501420 | CTGCAGTTCTTGTGG[C/G]GGGTGCCTCTGATCC | 89910 |
rs780311262 | snp | C/T | 1.65272e-05 | 0.0028746 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511276 | GTTGATCCTGCAGTA[C/T]ATCCCACATGTCATC | 89910 |
rs780348344 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540421 | TTGCCATATTGCCCA[C/T]GCTGGTCTTGAACTC | 89910 |
rs780380636 | snp | A/G | 1.69112e-05 | 0.0029078 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483688 | GGAGTTTTCTCTGTC[A/G]GAGTCGACTGCAGAG | 89910 |
rs780425977 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109486940 | CCAGTTAAGCAAGGA[A/G]GAGAACGTTGTGCTC | 89910 |
rs780476078 | snp | A/G | 1.69968e-05 | 0.00291515 | intron-variant | UBE3B | GRCh38.p7 | 12:109533683 | GCTGGACCCCTCAGA[A/G]CCAAGTGAGGAGGGC | 89910 |
rs780482789 | snp | A/T | 1.6823e-05 | 0.00290021 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507565 | TGTGTTTTTTCCAGG[A/T]CTCACTTACCTTGAT | 89910 |
rs780484204 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109531428 | GATCCTATCATTTCC[C/T]ACCAGCCTTCCTACT | 89910 |
rs780492742 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109536992 | GGGTGTATATCTTTG[C/T]AGTCCATGTTTTACA | 89910 |
rs780496224 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507685 | TGAAGAGTCCAAGCA[A/G]CTCTTGGCCATGCTG | 89910 |
rs780507038 | snp | A/G | 1.65496e-05 | 0.00287655 | intron-variant | UBE3B | GRCh38.p7 | 12:109483812 | AAAAGCCTTCCAGGT[A/G]CTACAAGCTGTTAAT | 89910 |
rs780528804 | in-del | -/ATAT | | | intron-variant | UBE3B | GRCh38.p7 | 12:109541845 | TCTGCCTCCATCCCC[-/ATAT]AGTCTTCCCTCTAGG | 89910 |
rs780534706 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512116 | GGCTCCTGGAAGCCA[C/T]TGGAAAGGGGGTCTG | 89910 |
rs780539134 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109520343 | GGCCTCAACAGATTA[A/G]AATCAAGAGACAAAC | 89910 |
rs780545883 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109488170 | AAGAAACTTGCCTAA[A/G]CTCACACAGCTAGTA | 89910 |
rs780574195 | snp | A/G | 1.65449e-05 | 0.00287614 | intron-variant | UBE3B | GRCh38.p7 | 12:109530093 | AGGCGGGTGGGGGGA[A/G]GGGTGAAATTCCTTG | 89910 |
rs780649712 | snp | C/T | 1.65127e-05 | 0.00287334 | intron-variant | UBE3B | GRCh38.p7 | 12:109483853 | TTTTTTTGCACTTTC[C/T]TTTCTAGGAGAGAGA | 89910 |
rs780685602 | snp | C/T | 0.000177794 | 0.00942683 | intron-variant | UBE3B | GRCh38.p7 | 12:109517886 | TCTCCCTCGGTGCAT[C/T]GTACCTTGTTTGTGT | 89910 |
rs780724429 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478151 | CAGTTTCCTTCTGTG[C/T]AAATGGAGTAATTAG | 89910 |
rs780804954 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109501150 | ATGGAGCTTGGGGAC[C/G]TGGGGAAAGCAGACA | 89910 |
rs780814928 | snp | A/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109506639 | TACAGGCGTGAGCCA[A/C]AGCACCGGGCTGCCA | 89910 |
rs780827180 | snp | C/G | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109501408 | ATCACCAAACAGCTG[C/G]AGTTCTTGTGGGGGG | 89910 |
rs780880141 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant, splice-acceptor-variant, missense, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109491043 | TAAAACATTCTTTTC[A/G]GATATTGTTAACCCG | 89910 |
rs780883789 | snp | G/T | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507597 | ACCTGCTTCCCAAAC[G/T]GTGGGCATTTATCTG | 89910 |
rs780883830 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109521183 | GCAGCTCTCCCAGCA[C/T]GCCATGAAGGGGGTC | 89910 |
rs780892707 | in-del | -/GA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527736 | GCCCAGCCAGGGCCA[-/GA]GAGAGAGCATGGTGA | 89910 |
rs780901409 | in-del | -/T | 3.40229e-05 | 0.00412435 | intron-variant | UBE3B | GRCh38.p7 | 12:109507554 | TTGGGTTTCTCTGTG[-/T]TTTTTCCAGGTCTCA | 89910 |
rs780925025 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495297 | CTATTGGAGCACATT[A/T]GCTAGAAGAAACCTT | 89910 |
rs780979678 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109527242 | GCTCTGCAGAATCTA[C/T]CATAAATGTCATCCT | 89910 |
rs780986770 | snp | A/G | 1.7423e-05 | 0.00295147 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109534730 | AGAAGAGCGTCCTCC[A/G]CGAGAAGCTGCGCTA | 89910 |
rs780998123 | snp | A/C | 3.72245e-05 | 0.00431403 | intron-variant | UBE3B | GRCh38.p7 | 12:109486590 | GGTAACAAAAAAAAA[A/C]AAAAAAAAAAAAAGC | 89910 |
rs781081455 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109498878 | TCACCCAGGCTGGAC[C/T]GCAGTGGCACAGTCA | 89910 |
rs781093271 | snp | A/C | 3.33678e-05 | 0.00408446 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109511301 | GTCATCCCTCACAAA[A/C]ACGTGAGTTGCACTC | 89910 |
rs781119404 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109495909 | GCATCACGGCCATCA[C/T]GAACATGTCACAATG | 89910 |
rs781150216 | snp | C/T | 1.72591e-05 | 0.00293756 | intron-variant | UBE3B | GRCh38.p7 | 12:109501584 | CACTTGGCTGAAGTA[C/T]AGCTCCTGTTTCTTC | 89910 |
rs781174586 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109515626 | CACCTGCCTCGGCCT[C/G]TCAAAGTGCTGGGAT | 89910 |
rs781259682 | snp | A/T | 1.95735e-05 | 0.00312832 | intron-variant | UBE3B | GRCh38.p7 | 12:109511172 | TGGTTTCCTTCTTTT[A/T]ATTCTCCCAAACCCA | 89910 |
rs781280361 | in-del | -/A | 5.10412e-05 | 0.00505154 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477289 | GACGCAGGAGTCTCC[-/A]AAACCCGGACTGAGA | 89910 |
rs781308027 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109502938 | CTGTGCATTTAGAGC[G/T]TTACTGAAATGCTCT | 89910 |
rs781317598 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109542431 | GTCACCAAATCCTCT[C/T]AATAGCTCTGAGATC | 89910 |
rs781340424 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109521865 | GAGGTGGAATTTGAA[C/T]CCAGGCCGGCCCAAG | 89910 |
rs781363141 | snp | G/T | | | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109490862 | TTGCCCTGTCACCCA[G/T]GCTGGCCTCAAGGAA | 89910 |
rs781370436 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532864 | TTGCACAGGGTCCCC[C/T]GGGGCCCCAGCACAT | 89910 |
rs781376412 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE3B | GRCh38.p7 | 12:109510114 | ACTTAAAAGGCCCTT[C/T]GGATGACACACTAGT | 89910 |
rs781382838 | snp | A/T | 3.29522e-05 | 0.00405894 | intron-variant | UBE3B | GRCh38.p7 | 12:109526345 | TATTAATTACTCCCA[A/T]CTTCTCCCCCAGCTT | 89910 |
rs781481928 | in-del | -/AA | | | intron-variant | UBE3B | GRCh38.p7 | 12:109509224 | ACATTATTTTGAAGC[-/AA]ATCCTAGACATCATA | 89910 |
rs781484866 | snp | C/G | 2.10968e-05 | 0.00324776 | intron-variant | UBE3B | GRCh38.p7 | 12:109499623 | CACACTCAGCCTTCT[C/G]TCTCTGTAGGCAACC | 89910 |
rs781503494 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109480263 | ACTATACACTCTACA[A/G]TGTGCACTCAAGTAC | 89910 |
rs781506345 | snp | C/G | 1.65334e-05 | 0.00287514 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109507717 | TGCTGTTCTGTGACT[C/G]TTCGCGGCACCTCAT | 89910 |
rs781547128 | snp | G/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109503041 | TCCTAAAGCGTGCTT[G/T]TCAAAAGTCGGCATC | 89910 |
rs781555443 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109497667 | CTGACTTGTCCATTT[C/T]CCCAGTGTATGTCCC | 89910 |
rs781557449 | snp | A/G | 6.59326e-05 | 0.00574125 | intron-variant | UBE3B | GRCh38.p7 | 12:109533452 | GTCCCCACTGACCCT[A/G]CTTTGTGTTGCAGTT | 89910 |
rs781600900 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540345 | CCCAGGTAGCTGGGA[C/G]CACAAGTGTGCATCA | 89910 |
rs781608135 | snp | C/T | 1.65373e-05 | 0.00287548 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109483955 | AGGAAACTGCTGTTC[C/T]TATTCAGAATCAAAG | 89910 |
rs781612620 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485539 | ATAGCCAAAATGGAA[C/T]CTGTTTTCTAGTTTC | 89910 |
rs781638290 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109498332 | GAAAGTTTAGAAGGA[C/T]GCCATACGCTTTGTC | 89910 |
rs781638655 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109510874 | ACTGAACATAGGCAT[A/G]TATCTGCATTTTTAT | 89910 |
rs781760960 | snp | A/G | 0.000185512 | 0.00962919 | intron-variant, synonymous-codon | UBE3B | GRCh38.p7 | 12:109534004 | CAAAGGAGAAGGAAA[A/G]CCTTCAGGGTTACGG | 89910 |
rs786205621 | in-del | -/CTC | | | cds-indel, nc-transcript-variant | UBE3B | GRCh38.p7 | 12:109509662 | AGAGCTGGTCACTAT[-/CTC]CTCTTTCCTGAATTC | 89910 |
rs796068500 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109493669 | ATCAGTGGTTTCATC[A/G]TATAGGAATATAGTG | 89910 |
rs796259687 | in-del | -/A | | | intron-variant | UBE3B | GRCh38.p7 | 12:109491559 | CAGAGAAGAGGTGAT[-/A]ATTTGCCTTCACTTA | 89910 |
rs796272286 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109513295 | GGTTCACGTGTGCTG[C/T]GGCCACTGGAGGTGC | 89910 |
rs796319716 | snp | A/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109528333 | TTCTCAGTAAAGTGG[A/T]GCAGTACTCGTCACC | 89910 |
rs796471974 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525619 | GATTTTTAGGTGATC[C/T]ACGGAAGTGTTCTTG | 89910 |
rs796480757 | in-del | -/C | | | intron-variant | UBE3B | GRCh38.p7 | 12:109512651 | TTGTAAATTAAATCT[-/C]ATTTTTCAGAGGTAT | 89910 |
rs796529250 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475628 | ATGTGGGACCAGGGC[C/T]TACTGCCACCTAGCT | 89910 |
rs796559892 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109533906 | AGAGTGGGCTCAGGA[A/G]GCAGGCAGGCGCAGA | 89910 |
rs796608851 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109490088 | TTGCATTCAGCATAC[C/T]TGGTGTCCTCCTCAG | 89910 |
rs796645044 | snp | A/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109485633 | GTGAGGCAAAAGTCA[A/G]TATCCATGGTGCTTA | 89910 |
rs796660080 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109540724 | TGTGAAGTCATTCTG[C/G]CCCTTCCAGGACTGC | 89910 |
rs796710490 | snp | C/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109532410 | ACTTTTTTTGATGCC[C/T]GACACACATAAACTG | 89910 |
rs796741593 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109537583 | CGTCCTCACAAGGAG[C/G]GTTCATGTAACTAAA | 89910 |
rs796766327 | snp | C/G | | | intron-variant | UBE3B | GRCh38.p7 | 12:109519546 | TAACCACAAACGCAT[C/G]TACTAATGCGTGTGA | 89910 |
rs796820953 | snp | G/T | | | intron-variant | UBE3B | GRCh38.p7 | 12:109525613 | TCCTTTGATTTTTAG[G/T]TGATCCACGGAAGTG | 89910 |
rs796825299 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479279 | ACAATAAAGCTCACT[-/T]ACATGCTACATGCTT | 89910 |