| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs192165570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76404058 | TCTACAGAGCAGAAT[A/G]CCAGCTAAAAGAAAT | 63893 |
| rs192269855 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76442840 | AGGAGGACTAGAGGC[A/G]GGGAGACCAGGGAGA | 63893 |
| rs192297454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76403703 | GCAATTAGCACACCT[A/G]GCATCCAGATCTTGG | 63893 |
| rs192343784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397445 | CTCTCCTTTCTCTCC[C/T]TCTCTGTTAGAGCTT | 63893 |
| rs192631453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413994 | AATGGTCAGTAATTC[A/C]GGCTGGTGCCAGTGT | 63893 |
| rs192642844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76392755 | GTCAGGAGTTCAAGA[A/G]CAGTCTGGCCAACGT | 63893 |
| rs192645367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434093 | CTAAGAAAGAAGTCT[A/G]TTTTCTTTGTCTGTG | 63893 |
| rs192690351 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | UBE2O | GRCh38.p7 | 17:76424197 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTTTTT | 63893 |
| rs192697190 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76393391 | GCTTCAGTCTCCTCA[C/T]GCCCGGCTAATTTTT | 63893 |
| rs192746119 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76450004 | GCTGAGGCAGGAGGA[C/T]TGTGTGAGACCAGGA | 63893 |
| rs192773816 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76421437 | CAATGGCGTGATCTC[A/G]GCACACCATAGCCTG | 63893 |
| rs192884885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449184 | AAAACTTGAGACTAA[C/G]ATTAAGCCTTTACTC | 63893 |
| rs192886965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76407676 | GAGTGCAGGGGAAAC[C/T]GAGGTGTCAACTCTG | 63893 |
| rs192914654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433297 | ATACATGCTACAACA[C/T]GGATGAACCTTGAAA | 63893 |
| rs192963976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439843 | ATCTCCTAATGCTCC[A/C]CACCACATCCTTCAG | 63893 |
| rs192975384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397742 | TACACGCCTGTGGCC[C/T]CCGGCCCAAGTTGCC | 63893 |
| rs193108843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429636 | CTCTGGACAGGTGAG[G/T]ACCACATTAGATGGA | 63893 |
| rs193125452 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76425317 | CATATTGTATTTTTT[A/T]AAATAATAGTTTAGC | 63893 |
| rs193126669 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452272 | GGATTTTCACCTCTA[C/T]CTTTGTTTTGGAATG | 63893 |
| rs193156008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411789 | CACCTGGGCTCAAGT[A/T]ATCCTTCTGCCTCAG | 63893 |
| rs193282444 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76443929 | GAAATACCGTTAAGA[C/G]GGCATGGTCGGCCAG | 63893 |
| rs199508873 | in-del | -/TA | 0.0441155 | 0.141815 | intron-variant | UBE2O | GRCh38.p7 | 17:76416104 | ATACATGTATATGCG[-/TA]TGTGTATACATATAT | 63893 |
| rs199532822 | in-del | -/TT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397436 | GGGTCGGCTCTCTCC[-/TT]TCTCTCCTTCTCTGT | 63893 |
| rs199546447 | snp | C/T | 1.66924e-05 | 0.00288893 | synonymous-codon, intron-variant | UBE2O | GRCh38.p7 | 17:76400150 | CCAAGGACATACCTT[C/T]TTGGCCATAGAGCCC | 63893 |
| rs199568080 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396363 | GTTTTCCTGTAGCTT[C/T]TTGATGTCATCCAGA | 63893 |
| rs199615423 | snp | C/T | 9.8894e-05 | 0.00703116 | missense | UBE2O | GRCh38.p7 | 17:76396260 | CAGGTGACTGCCCCT[C/T]GGGCTTGTCCTCCTT | 63893 |
| rs199618431 | snp | C/T | 0.000174902 | 0.00934988 | missense | UBE2O | GRCh38.p7 | 17:76399914 | TGCTTCTTCAACAGG[C/T]GCTTCACCTGCAAGG | 63893 |
| rs199680423 | snp | A/G | 0.00103727 | 0.0227499 | missense | UBE2O | GRCh38.p7 | 17:76399543 | GGATGCTCTTTTTGC[A/G]ACTCGTGCCGCTGCC | 63893 |
| rs199702344 | snp | A/G | 1.7525e-05 | 0.0029601 | intron-variant | UBE2O | GRCh38.p7 | 17:76400424 | CCCTGGGTTGCTGGC[A/G]GTAAGGGCATGCTTA | 63893 |
| rs199731811 | snp | A/G | 0.00649417 | 0.0566119 | intron-variant | UBE2O | GRCh38.p7 | 17:76405185 | CCCAGAAAGGATGAT[A/G]AGAAGACAGGGCCGG | 63893 |
| rs199817180 | snp | A/C | 0.000562197 | 0.0167566 | intron-variant | UBE2O | GRCh38.p7 | 17:76391831 | GAAACACACAGGGCA[A/C]CATCAATTCTGTTCC | 63893 |
| rs199844330 | in-del | -/AAATAAAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423694 | GGACACTCCATCTCA[-/AAATAAAT]AAATAAATAAATAAA | 63893 |
| rs199845309 | in-del | -/C | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389510 | GCTAATGAGCCAACA[-/C]AAAAAAAAAAAAAAA | 63893 |
| rs199863143 | in-del | -/AA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446458 | TGAAAAAACAAAAAC[-/AA]AAACAAAAAAAAAAA | 63893 |
| rs199929032 | snp | C/G | 0.00068266 | 0.0184625 | intron-variant | UBE2O | GRCh38.p7 | 17:76400577 | AGGTGGGACACGCCA[C/G]TCAGGGCAGGCTCTG | 63893 |
| rs199944977 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433617 | TAAACCTTTTTTTTT[A/T]TAAGAGATGGGGTCT | 63893 |
| rs199954654 | in-del | -/TATG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416034 | GTACACACACGTATA[-/TATG]TGTGTGTACATATGT | 63893 |
| rs199955445 | snp | A/C | 0.000230719 | 0.0107381 | missense | UBE2O | GRCh38.p7 | 17:76398258 | TTGAAGGCGTACCTC[A/C]TCCTCCTTGTGAGGA | 63893 |
| rs199992045 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424870 | TTTTTTTTATTTTTT[A/T]TTTTTTTTTTTTGAG | 63893 |
| rs200006271 | snp | A/G | 4.94344e-05 | 0.00497139 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398267 | TACCTCATCCTCCTT[A/G]TGAGGAGCCCCATCC | 63893 |
| rs200035390 | snp | G/T | 0.0139594 | 0.08237 | stop-gained | UBE2O | GRCh38.p7 | 17:76391069 | GAAGCCGATGTCAGG[G/T]TAGCCACTCTTCTCA | 63893 |
| rs200057437 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76392119 | AGAAGAGGTCCTAGG[G/T]AGGGAGGGAGGGAGG | 63893 |
| rs200124853 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412924 | GAGGCAGGAGAATCG[C/T]TTGAACCCGGGAGGC | 63893 |
| rs200167973 | snp | C/G/T | 8.2854e-05 | 0.00643591 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396708 | CACCAGCCCATTGTC[C/G/T]GTCTCCCAGCTGTCA | 63893 |
| rs200186813 | snp | C/T | 0.000639311 | 0.0178675 | missense | UBE2O | GRCh38.p7 | 17:76402087 | TGACGTGCGGGCAGA[C/T]GTCGTAGAGCTTGGC | 63893 |
| rs200190308 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442095 | TAGGCGGGGTTCTTA[-/C]AGGGGAAATGCAGCC | 63893 |
| rs200206239 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395055 | TAATTTTTGTATTTT[A/T]AGTAGAGACAGGGTT | 63893 |
| rs200206989 | snp | A/G | 0.000399281 | 0.0141238 | missense | UBE2O | GRCh38.p7 | 17:76391163 | TCTGGTGCGGTCTCC[A/G]AAGTCTGGTCTGTGT | 63893 |
| rs200208578 | snp | C/T | 3.52026e-05 | 0.00419524 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76390964 | GTCCTCTGTGCACTC[C/T]GGCATGCCTGCCTCT | 63893 |
| rs200219712 | snp | A/G | 1.65477e-05 | 0.00287638 | intron-variant | UBE2O | GRCh38.p7 | 17:76395877 | CTAGAGGGGGGAAGA[A/G]AATAGTCAGTCCCTC | 63893 |
| rs200317048 | in-del | -/T | 0.232359 | 0.249377 | intron-variant | UBE2O | GRCh38.p7 | 17:76426914 | CTTAGTAAATACAAC[-/T]TTTTTTTTTTTCTGT | 63893 |
| rs200328484 | snp | C/T | 8.29993e-05 | 0.00644149 | missense | UBE2O | GRCh38.p7 | 17:76391461 | CCTGCTCAAAGACCT[C/T]GGGGGGCCGCCGCAC | 63893 |
| rs200340348 | snp | A/G | 8.23811e-05 | 0.00641746 | missense | UBE2O | GRCh38.p7 | 17:76399650 | TCTGCGTCCTGCTCT[A/G]CCGAGTGCAGCCTGT | 63893 |
| rs200415901 | snp | A/G | 1.82214e-05 | 0.00301834 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391979 | GTTGGGGTTCAGGCG[A/G]CCACTGCATTGGGAG | 63893 |
| rs200497213 | snp | C/G | 0.000140336 | 0.00837546 | intron-variant | UBE2O | GRCh38.p7 | 17:76405478 | TAAGGTGGCTGCCCC[C/G]AGGCCCGGGGCTGGG | 63893 |
| rs200535974 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431652 | GGTAGGGAAAAGAAA[A/G]ACTATTAGGGCCAGA | 63893 |
| rs200553803 | snp | C/T | 1.68391e-05 | 0.0029016 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396627 | CACCACTCCCTTGTC[C/T]TCAGGGGCCACCGGC | 63893 |
| rs200595829 | snp | C/T | 0.0039921 | 0.0444985 | intron-variant | UBE2O | GRCh38.p7 | 17:76395673 | TGGTGGCCTCTTGGG[C/T]ACTGGGTGCCCACAC | 63893 |
| rs200605073 | snp | A/G | 1.65029e-05 | 0.00287248 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391784 | GAGCACCTGGAGAAG[A/G]CTGGACTTGCTTGTC | 63893 |
| rs200616282 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424910 | CGCCCTCACCCTGTC[A/T]CCCAGGCTGGAGTGC | 63893 |
| rs200665791 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423548 | AATACAAAAAATTAG[C/T]CAGGCATGGTGGCAC | 63893 |
| rs200678618 | snp | A/C/T | 9.9054e-05 | 0.00703685 | intron-variant | UBE2O | GRCh38.p7 | 17:76398226 | CAGGGCAGTGAGCAG[A/C/T]CATCCAGAACTTGAA | 63893 |
| rs200685368 | snp | C/T | | | synonymous-codon, intron-variant | UBE2O | GRCh38.p7 | 17:76400171 | CATAGAGCCCTCCCC[C/T]TGGGCGCAGTTTTTT | 63893 |
| rs200705112 | in-del | -/T | 0.416382 | 0.186593 | intron-variant | UBE2O | GRCh38.p7 | 17:76394880 | AATTTTTTTTTTTTT[-/T]GAGATGAAGTCTCGC | 63893 |
| rs200785455 | in-del | -/TCTC | 0.0205511 | 0.0992634 | intron-variant | UBE2O | GRCh38.p7 | 17:76425863 | CAGAATTCCATCCTG[-/TCTC]TCTAACTCAGACTTT | 63893 |
| rs200786237 | snp | C/T | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389445 | GGGACACAAAGGCAA[C/T]GGAGCCCAGATGAAT | 63893 |
| rs200804649 | snp | C/G | 0.000271368 | 0.0116452 | intron-variant | UBE2O | GRCh38.p7 | 17:76396826 | TTGTACAAGTGCTGG[C/G]GGCAGAAGGGAAGTG | 63893 |
| rs200806608 | snp | A/G | 9.90688e-05 | 0.00703737 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391060 | GAAGAGGGGGAAGCC[A/G]ATGTCAGGGTAGCCA | 63893 |
| rs200976427 | snp | A/C | 0.00199806 | 0.0315443 | missense | UBE2O | GRCh38.p7 | 17:76401104 | GATCTTGGCAGGGCC[A/C]ATGAGCACCTGGCCT | 63893 |
| rs201072765 | snp | A/C | 5.34088e-05 | 0.00516735 | intron-variant | UBE2O | GRCh38.p7 | 17:76402014 | CGAAGTCCTCCTTCC[A/C]GAGGACTGAGCAATC | 63893 |
| rs201081174 | snp | C/G | 0.000331824 | 0.0128764 | intron-variant | UBE2O | GRCh38.p7 | 17:76397894 | CCACCGATGGCTGCT[C/G]GGCAAAGGGGACAAA | 63893 |
| rs201129970 | snp | A/G | 4.08914e-05 | 0.00452151 | intron-variant | UBE2O | GRCh38.p7 | 17:76400554 | TACAACCTGCACCTG[A/G]GGATGGCAGGTGGGA | 63893 |
| rs201152699 | snp | C/G | 3.34778e-05 | 0.00409119 | missense | UBE2O | GRCh38.p7 | 17:76399862 | ATGGTCCCGGGAACA[C/G]TGGGTGTCTGGGGAG | 63893 |
| rs201187862 | snp | C/T | 0.000222471 | 0.0105445 | intron-variant | UBE2O | GRCh38.p7 | 17:76399421 | TTCACGCTGACGCCA[C/T]TGGGGAGGGGCACAA | 63893 |
| rs201218957 | in-del | -/T | 0.00716266 | 0.059414 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389795 | GCATCATGCTTTGGC[-/T]TTTTTTTTTGTCTTT | 63893 |
| rs201241277 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407532 | ACCATGTGTGGCAGG[A/G]GGGCTGCCTCCACCA | 63893 |
| rs201264179 | snp | C/T | 4.95103e-05 | 0.00497521 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396216 | CTGCTGGCACAGCAC[C/T]GGGGTTTCGCTGGGC | 63893 |
| rs201273063 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412932 | AGAATCGTTTGAACC[C/T]GGGAGGCGGAGGTTG | 63893 |
| rs201376977 | snp | G/T | 0.000153988 | 0.00877328 | missense | UBE2O | GRCh38.p7 | 17:76400530 | GGTAATCCATGTAAC[G/T]TTCAACTCTACAACC | 63893 |
| rs201449534 | in-del | -/C | 0.180702 | 0.240204 | intron-variant | UBE2O | GRCh38.p7 | 17:76446463 | AAACAAAAACAAACA[-/C]AAAAAAAAAACCAAA | 63893 |
| rs201472411 | snp | A/G | 3.31055e-05 | 0.00406837 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396723 | CGTCTCCCAGCTGTC[A/G]CTATCATCTTCCCAT | 63893 |
| rs201483522 | snp | A/G | 0.000132604 | 0.00814152 | intron-variant | UBE2O | GRCh38.p7 | 17:76391730 | GGCCCTCCCTTGTCC[A/G]CACCCCCGCTTCAGC | 63893 |
| rs201492674 | in-del | -/AAAAAGC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440129 | AGGTGCTATGAGGGA[-/AAAAAGC]TGAGTAGGAGATCAC | 63893 |
| rs201526520 | snp | C/T | 1.65031e-05 | 0.00287251 | intron-variant | UBE2O | GRCh38.p7 | 17:76398231 | CAGTGAGCAGCCATC[C/T]AGAACTTGAATTTGA | 63893 |
| rs201543604 | in-del | -/AC | 0.172028 | 0.23753 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389507 | CTTGCTAATGAGCCA[-/AC]ACAAAAAAAAAAAAA | 63893 |
| rs201550259 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant | UBE2O | GRCh38.p7 | 17:76391620 | GGATCAGACCTGTGT[A/G]GGCGGGACACCTTCC | 63893 |
| rs201557543 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423896 | CTTCCAGGTTGGGTT[C/T]TTTTTTTTTTTTTTT | 63893 |
| rs201575312 | in-del | -/ACACACACACAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435406 | AATATACAGATACAC[-/ACACACACACAT]ACACACACACACACA | 63893 |
| rs201596350 | in-del | -/AGGAGGAA | 0.0205511 | 0.0992634 | intron-variant | UBE2O | GRCh38.p7 | 17:76417704 | AGGGCCTTCGACTAC[-/AGGAGGAA]AGAATGCTAAGCATG | 63893 |
| rs201638285 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443595 | TGCCCAGTCAGAACA[A/T]TTTTTTTTTTTTTAA | 63893 |
| rs201652216 | snp | A/G | 0.000119327 | 0.00772328 | missense | UBE2O | GRCh38.p7 | 17:76400472 | GGGTGATGACAGAGG[A/G]TGGGGGGCTGACGCT | 63893 |
| rs201664546 | snp | A/C | 0.180702 | 0.240204 | intron-variant | UBE2O | GRCh38.p7 | 17:76446469 | AAAACAAACAAAAAA[A/C]AAAACCAAACAAACA | 63893 |
| rs201696419 | snp | A/G | 0.00199805 | 0.0315441 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398559 | CTGTACCACACCGTA[A/G]ACAGCAGGGTCTGGA | 63893 |
| rs201750774 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405308 | GATCACCGTGCCACA[C/T]TGACTGTCCTGGGGG | 63893 |
| rs201764614 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442096 | AGGCGGGGTTCTTAC[A/G]GGGGAAATGCAGCCA | 63893 |
| rs201796669 | snp | G/T | 3.30732e-05 | 0.00406638 | missense | UBE2O | GRCh38.p7 | 17:76391205 | GCTGAGGCCAGGCCC[G/T]GGGCACCGCCCTCTG | 63893 |
| rs201816148 | in-del | -/GGGTGT | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451778 | GTGTGAGATACAGGG[-/GGGTGT]GTGTGTGTGTGTGTG | 63893 |
| rs201880760 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412940 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 63893 |
| rs201921441 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424849 | TAATTTCACCTGTTT[C/T]TTTTTTTTTTTTTAT | 63893 |
| rs201937397 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431504 | AGGGTGCTCTGTCTC[-/A]AAAAAAAAAGTCAAC | 63893 |
| rs201970029 | snp | C/T | 0.000861469 | 0.0207363 | intron-variant | UBE2O | GRCh38.p7 | 17:76391840 | AGGGCACCATCAATT[C/T]TGTTCCCCAGGCCCC | 63893 |
| rs201974775 | snp | A/G | 0.0039921 | 0.0444985 | intron-variant | UBE2O | GRCh38.p7 | 17:76396827 | TGTACAAGTGCTGGG[A/G]GCAGAAGGGAAGTGC | 63893 |
| rs201981235 | snp | C/T | 0.00154013 | 0.0277073 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76397883 | GGCCACCTGGCCCAC[C/T]GATGGCTGCTGGGCA | 63893 |
| rs201983628 | snp | C/T | 0.000219994 | 0.0104856 | intron-variant | UBE2O | GRCh38.p7 | 17:76391623 | TCAGACCTGTGTGGG[C/T]GGGACACCTTCCCTC | 63893 |
| rs201991279 | snp | C/T | 0.000461559 | 0.0151844 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398538 | ACGGCCGATGTGGTC[C/T]CCAGACTGTACCACA | 63893 |
| rs202002025 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441275 | TGGGTGTGTTATACT[A/C]AAAACAACTACCATA | 63893 |
| rs202009838 | in-del | -/TATATG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416032 | ATGTACACACACGTA[-/TATATG]TGTGTGTACATATGT | 63893 |
| rs202061651 | snp | C/T | 0.000267076 | 0.0115528 | missense | UBE2O | GRCh38.p7 | 17:76391404 | AGGACTCGATACGGT[C/T]CACCAGCCGCCAGCC | 63893 |
| rs202081283 | snp | A/G | 3.29609e-05 | 0.00405948 | missense | UBE2O | GRCh38.p7 | 17:76402699 | CCCCATACATGAAGG[A/G]CTGCAGACCAAGGAG | 63893 |
| rs202108643 | in-del | -/T/TT | 0.055478 | 0.158255 | intron-variant | UBE2O | GRCh38.p7 | 17:76443295 | GAATATATATATATA[-/T/TT]TTTTTTTCCTCGAGA | 63893 |
| rs202120728 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442100 | GGGGTTCTTACAGGG[C/T]AAATGCAGCCAGAAG | 63893 |
| rs202122073 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429016 | AAGCAATTCTCCTGC[C/T]TCAGCCTCCCGAGTA | 63893 |
| rs202124321 | in-del | -/G | 0.0166325 | 0.0896639 | intron-variant | UBE2O | GRCh38.p7 | 17:76391685 | ACCCTCCACCTGCCA[-/G]GGGGACTATCAGAGT | 63893 |
| rs202144250 | snp | A/C/G | 0.00201882 | 0.0317125 | intron-variant | UBE2O | GRCh38.p7 | 17:76401204 | AGCGGTGTCTCCATG[A/C/G]GTGACCATGCTCTCC | 63893 |
| rs202165048 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392312 | GAACAGCCTGGAATC[C/T]TTTTTTTTTGAGACA | 63893 |
| rs202208955 | snp | A/C | 0.000862169 | 0.0207447 | intron-variant | UBE2O | GRCh38.p7 | 17:76395902 | TCCCTCATGGAGAGG[A/C]CCTGGAGCTCCATCT | 63893 |
| rs267605060 | snp | C/T | | | missense | UBE2O | GRCh38.p7 | 17:76402111 | GCTTGGCGCCATCTT[C/T]CGTGTTCATGGAGCA | 63893 |
| rs267605061 | snp | A/G | | | missense | UBE2O | GRCh38.p7 | 17:76405237 | TCCTTGCTGTTGACG[A/G]GATAGATGATGCAGT | 63893 |
| rs367556687 | snp | A/G | 0.000153988 | 0.00877328 | missense | UBE2O | GRCh38.p7 | 17:76395853 | CAATTTTCTTAAAAG[A/G]ATGATTTGCTAGAGG | 63893 |
| rs367630532 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427897 | AACTCCATGCTTCAC[A/G]TGTTCATGCAAATCC | 63893 |
| rs367658458 | snp | C/G | 9.91867e-05 | 0.00704155 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400252 | ATACAGACAGCGCTC[C/G]CCAAGCTGCCGCTGA | 63893 |
| rs367751872 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419837 | GAAGGGAGCGAGCTG[G/T]TGTGAAAGCGTGGCT | 63893 |
| rs367762677 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436169 | GGAGAATTGCTTGAA[C/T]CCGGGAGGCGGAGGT | 63893 |
| rs367812947 | snp | A/G | 7.52389e-05 | 0.00613301 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390914 | GCTGGCCTCTCCCAC[A/G]GTGATGCTCTTTCCT | 63893 |
| rs367836180 | snp | C/T | 0.000149919 | 0.00865661 | missense | UBE2O | GRCh38.p7 | 17:76391412 | ATACGGTTCACCAGC[C/T]GCCAGCCACCAGTGC | 63893 |
| rs367858837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76399390 | GCACACCGAGGGGAC[A/G]CGCACTCTGCCTGGC | 63893 |
| rs367864952 | snp | A/T | 0.000217991 | 0.0104378 | intron-variant | UBE2O | GRCh38.p7 | 17:76400338 | GCTGGGCTGGACTCC[A/T]GGGAGGCCAGCAGTG | 63893 |
| rs367870567 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417127 | AGCTCCAGGCCCTTC[C/T]GGCTACAGCTCCAGA | 63893 |
| rs367873169 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76432937 | TGACAGTCACAAGCA[C/T]TGGTGAGCATGTGGA | 63893 |
| rs367897734 | snp | C/T | 3.33778e-05 | 0.00408507 | intron-variant | UBE2O | GRCh38.p7 | 17:76399001 | GCCACCCTGCGGGTG[C/T]AGGCCAGTCAGCAGG | 63893 |
| rs367905486 | snp | C/T | 6.59283e-05 | 0.00574106 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396435 | AGAGGTGGGCGAGCC[C/T]GTCAGCAGCTGCTCC | 63893 |
| rs367951178 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419999 | GCAACTGCGAATGCA[C/T]AGAAGCATGACATAA | 63893 |
| rs368053131 | snp | A/G | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389191 | ACTACAGCTGCTGGG[A/G]GGCTGCTCTAAGCTG | 63893 |
| rs368135488 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394696 | TTTGGAAGGAGACCC[A/G]CTAAACTTCCAACAA | 63893 |
| rs368179537 | snp | A/G | 7.57906e-05 | 0.00615545 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390895 | GGGGAGTGAGCAGGC[A/G]GCGGCTGGCCTCTCC | 63893 |
| rs368232493 | snp | C/G | 5.0671e-05 | 0.00503318 | intron-variant | UBE2O | GRCh38.p7 | 17:76398593 | CTCTGGACTAGGGAA[C/G]CAGAGAAAGGGAAGT | 63893 |
| rs368245168 | snp | A/G | 1.65512e-05 | 0.00287669 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398565 | CACACCGTAGACAGC[A/G]GGGTCTGGACAGCTC | 63893 |
| rs368318418 | snp | C/T | 1.65228e-05 | 0.00287422 | missense | UBE2O | GRCh38.p7 | 17:76391569 | GGCCTCGGTCACTGT[C/T]GAAGCCGGCTTCGTT | 63893 |
| rs368324324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397745 | ACGCCTGTGGCCCCC[A/G]GCCCAAGTTGCCATA | 63893 |
| rs368378503 | snp | A/C | 1.70159e-05 | 0.00291679 | missense | UBE2O | GRCh38.p7 | 17:76396773 | TGGTGCTGCCTTCTA[A/C]CGAATCGTAGTCTGA | 63893 |
| rs368379476 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402688 | GGCAATGTAGTCCCC[A/G]TACATGAAGGGCTGC | 63893 |
| rs368395116 | snp | A/G | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390164 | ACTTGCCCTGGCCTT[A/G]TGCAGCTGCTCTTGC | 63893 |
| rs368400268 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76423452 | TAATCCCAGCACTTC[A/G]GGAGGCCGAGGTGGG | 63893 |
| rs368411420 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398841 | GCTGGCACTACCTCG[C/T]TTATCTACCACGAAG | 63893 |
| rs368494524 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446662 | CTCAGCATTCCCAGC[C/T]GAAGGATGACAGCAG | 63893 |
| rs368516552 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395405 | CACTGTGTTAGCCAG[C/G]ATGGTCTCGATCTCC | 63893 |
| rs368523942 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438260 | CTGGGGGTGGATGGT[G/T]GGGATGGTTGCACAA | 63893 |
| rs368533534 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427037 | GATTTTACTTCCTTA[C/T]GGCCTCTACTGTTGC | 63893 |
| rs368550366 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455173 | GCTCACGCCTGAAAT[C/T]CCAACACTTTGACTG | 63893 |
| rs368560276 | snp | G/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390391 | TATAGCCGGGAGTCA[G/T]TGACAGCAGCTACAA | 63893 |
| rs368572923 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76397820 | CAGGATGATGGTCTT[C/T]GAGTTGTCAGCCCAC | 63893 |
| rs368576807 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435318 | TGAAAATGGTAGGAG[A/G]GAGACAAACATTTCA | 63893 |
| rs368628714 | snp | C/T | 0.00151458 | 0.0274772 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76401032 | CACCACCACTCGGAA[C/T]TTGCTCTTGGTGCTG | 63893 |
| rs368650758 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76437480 | GAAAAAGAAAAAAAA[-/A]GGCAATTATGTTAAA | 63893 |
| rs368695410 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413677 | ACCTGCGCCGACTCT[C/T]GGTCCTTTCTGGCCA | 63893 |
| rs368720072 | snp | C/T | 8.38933e-05 | 0.00647608 | missense | UBE2O | GRCh38.p7 | 17:76391296 | CGGAGTCTGACAGCT[C/T]GGCTACAGCTGGGGG | 63893 |
| rs368880051 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420791 | CTGCCAGCATTCAAA[A/G]TCGGCCTGCCACACA | 63893 |
| rs368942445 | snp | A/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390311 | CGGAACCTAGCCTGG[A/T]CCCAACCTCTCTTAG | 63893 |
| rs368949620 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450319 | CAGACCAGGAGACAT[C/T]CAGCTAATCAGTCAC | 63893 |
| rs368991683 | snp | A/G | 3.31225e-05 | 0.00406941 | intron-variant | UBE2O | GRCh38.p7 | 17:76391837 | CACAGGGCACCATCA[A/G]TTCTGTTCCCCAGGC | 63893 |
| rs369002553 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452390 | GCCGCACTGGTGTAA[C/G]GCCGAACGCGCCCCA | 63893 |
| rs369070451 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | UBE2O | GRCh38.p7 | 17:76399735 | GCTCCTCTGCACCCT[C/T]GTCCTGCATCTCCAC | 63893 |
| rs369083653 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407231 | CACTGGCCCTGTGAG[C/T]TGCAGGGTGAAGACC | 63893 |
| rs369118884 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404759 | ATGTTTTGGGAAGAA[A/G]AAAGACCGGAGGGGG | 63893 |
| rs369147166 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452115 | CCCAAGTACTATTCA[C/T]ACCGGGGCTCTGATT | 63893 |
| rs369169412 | snp | G/T | 5.07627e-05 | 0.00503774 | intron-variant | UBE2O | GRCh38.p7 | 17:76400971 | GCTCCAGGGTGTGGA[G/T]GTCAAGGACTCCATC | 63893 |
| rs369176132 | snp | G/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390383 | AGGCCATGTATAGCC[G/T]GGAGTCAGTGACAGC | 63893 |
| rs369336104 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411444 | CACTAGCACCAGCAT[G/T]TGAACACTAAATGGG | 63893 |
| rs369336849 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76406886 | TGTATTTTTAGTAGA[C/G]ATGGGGCTTCACCAT | 63893 |
| rs369396247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428941 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 63893 |
| rs369400615 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415675 | CTGGGTGTGGTGGTG[C/T]GCACCTGTAATCCCA | 63893 |
| rs369505696 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427352 | GATTCTTTAAAAAAT[A/G]ATCCCTTTTAAGATG | 63893 |
| rs369517143 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410656 | GTGGCAGGAGGCTGG[A/G]CACTTCTGTTGTGCC | 63893 |
| rs369517491 | snp | C/T | 0.000134957 | 0.00821343 | intron-variant | UBE2O | GRCh38.p7 | 17:76391871 | TATCCACCAGTGGCT[C/T]TTCCTCCTTCTTGGC | 63893 |
| rs369523561 | in-del | -/GAGGAAAG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417706 | GGCCTTCGACTACAG[-/GAGGAAAG]AATGCTAAGCATGTC | 63893 |
| rs369525391 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442508 | TGAAGATGTTTCCCA[A/G]GAGTCTGCATGTGCG | 63893 |
| rs369624493 | snp | C/T | 1.67565e-05 | 0.00289447 | intron-variant | UBE2O | GRCh38.p7 | 17:76397936 | CAGCTCAAGCTCCAG[C/T]TCCCCAGCCCCTCCT | 63893 |
| rs369628430 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407590 | GAAAGGAGGAGAGAA[A/G]AACGCAGACACAGAC | 63893 |
| rs369675245 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393367 | CCTCCCAGGTTCAAG[C/T]GATTCTCTGCTTCAG | 63893 |
| rs369700634 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76402444 | CCACGGCAGATAAGG[A/C]GAACGGTACAGGGTT | 63893 |
| rs369705758 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76406840 | GAGTAGGTGGGACTG[C/G]AGGCACGTGCCACCA | 63893 |
| rs369707672 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399658 | CTGCTCTGCCGAGTG[C/T]AGCCTGTCATCTCTG | 63893 |
| rs369738788 | snp | C/T | 0.000549923 | 0.0165728 | intron-variant | UBE2O | GRCh38.p7 | 17:76400402 | CAGAGCCCTGTCCCA[C/T]GCGTGCCCCTGGGTT | 63893 |
| rs369775609 | snp | G/T | 0.00013913 | 0.00833942 | intron-variant | UBE2O | GRCh38.p7 | 17:76405190 | AAAGGATGATGAGAA[G/T]ACAGGGCCGGCTCAC | 63893 |
| rs369791949 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429165 | TCGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCA | 63893 |
| rs369867426 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395050 | CCGGCTAATTTTTGT[A/G]TTTTTAGTAGAGACA | 63893 |
| rs369950547 | snp | A/C/T | 8.3181e-05 | 0.00644863 | intron-variant | UBE2O | GRCh38.p7 | 17:76391714 | GTCACTTTCCTCCAC[A/C/T]GGCCCTCCCTTGTCC | 63893 |
| rs369975381 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404016 | TAAAAAAAAAGAATA[C/T]ATAAATAGGGCAGAA | 63893 |
| rs369978032 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76421588 | CAGGCTGGTCTTGAA[C/T]TTCCGACCTCAGGTG | 63893 |
| rs369991298 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417714 | ACTACAGGAGGAAAG[A/G]ATGCTAAGCATGTCC | 63893 |
| rs370018691 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399233 | CAGAAGGCCAAGCTT[A/G]AGGCCACCACCATCC | 63893 |
| rs370023180 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450976 | ACTCTGTATAATTAC[A/C]CATAGTGCAGGAGGC | 63893 |
| rs370100297 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452079 | TCATCAATCCCGGTC[A/G]CAGCTGTCAGAATCC | 63893 |
| rs370101730 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBE2O | GRCh38.p7 | 17:76400437 | GCAGTAAGGGCATGC[C/T]TACCTGCCTAGGTTT | 63893 |
| rs370251725 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408053 | GGGAGGCTCTTGTGA[C/T]TTTCCTTCCTAACTT | 63893 |
| rs370272992 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425028 | GGCACCCGCCACCAC[A/G]CCCAGCTAACTTTTT | 63893 |
| rs370274546 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440409 | CACGGCCCATTGCCA[C/G]CTCGACCGCCAGGAC | 63893 |
| rs370367744 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408481 | AGGCAGTTTGGCTCC[A/G]GAGTCCATTCTCTTA | 63893 |
| rs370410096 | snp | C/G | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454095 | TTCGATAAGCTTAAC[C/G]ATTGTTGTACTATTT | 63893 |
| rs370421905 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76425636 | CAACAGTTCCACTGC[A/T]TTAATTGAAAAATCT | 63893 |
| rs370506474 | snp | C/T | 0.000153988 | 0.00877328 | missense | UBE2O | GRCh38.p7 | 17:76396521 | AGCTCTTGGGTGGCC[C/T]GTCCTTGCCAGCCTT | 63893 |
| rs370517188 | snp | A/G | 1.67654e-05 | 0.00289524 | missense | UBE2O | GRCh38.p7 | 17:76396662 | CCAGGGGTGGGATGG[A/G]GGGCTCCTCTATCTT | 63893 |
| rs370524048 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409189 | TAGCCACGATGCTCT[C/T]GATCTCCTAACCTCG | 63893 |
| rs370599980 | in-del | -/CAAGTTCTAGGCTGCATCC | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76402869 | AGCAGGCCCTCCCTA[-/CAAGTTCTAGGCTGCATCC]CAGCTGCTCTTCCCA | 63893 |
| rs370664701 | snp | A/G | 0.000106589 | 0.00729953 | intron-variant | UBE2O | GRCh38.p7 | 17:76399929 | CGCTTCACCTGCAAG[A/G]GCGGAGCAGAGAGGA | 63893 |
| rs370722718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418260 | GCCCACAGCCTCCCG[A/G]AGGGCTCTCCAGGCC | 63893 |
| rs370727151 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413639 | GCTGGAGAATCTCCA[C/T]TCTACTGAATTCTCT | 63893 |
| rs370773712 | snp | C/G | 0.0111196 | 0.0737302 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452595 | GTGTACCCTCCACTG[C/G]GGCTGTCCTCCCGCG | 63893 |
| rs370813249 | snp | A/C/G | 3.78582e-05 | 0.00435062 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390898 | GAGTGAGCAGGCGGC[A/C/G]GCTGGCCTCTCCCAC | 63893 |
| rs370836885 | snp | C/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389984 | GGGCCTGTCTCTGGG[C/T]ACTAGGAGAGCCCCC | 63893 |
| rs370887693 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430633 | CTGTCAAAGCAATTC[A/G]CTTCTTATTGATTTT | 63893 |
| rs370904103 | snp | A/G | 0.00193372 | 0.0310342 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452721 | CAGCCCCCGCCCGCC[A/G]CACCTTGGTCTCCTT | 63893 |
| rs370912660 | snp | A/G | 1.66493e-05 | 0.0028852 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76401053 | CTTGGTGCTGAGCAC[A/G]GGCTTGACACCTGAC | 63893 |
| rs370939220 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE2O | GRCh38.p7 | 17:76391902 | TGGGGGCCTGGCCCT[A/G]TACTCACCTTTCCAA | 63893 |
| rs371018680 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76400800 | TCCCACCTTGCTCAG[C/T]CTGTACAGGCTGGGC | 63893 |
| rs371045437 | snp | C/T | 0.000333628 | 0.0129113 | missense | UBE2O | GRCh38.p7 | 17:76391281 | CAGGTTCTTGTTGGC[C/T]GGAGTCTGACAGCTC | 63893 |
| rs371076398 | snp | C/T | 6.59544e-05 | 0.0057422 | intron-variant | UBE2O | GRCh38.p7 | 17:76398250 | ACTTGAATTTGAAGG[C/T]GTACCTCATCCTCCT | 63893 |
| rs371076705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76404093 | GGAACAAGGGAGTCA[C/T]AGAACCACCATTTAG | 63893 |
| rs371087938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446230 | CATGTCACAGAAAAC[C/T]ACCCTGACTCCAACT | 63893 |
| rs371091639 | in-del | -/CTCT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425866 | AATTCCATCCTGTCT[-/CTCT]AACTCAGACTTTCCT | 63893 |
| rs371101042 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | UBE2O | GRCh38.p7 | 17:76391690 | CCACCTGCCAGGGGG[A/T]CTATCAGAGTCACTT | 63893 |
| rs371105335 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412899 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 63893 |
| rs371135396 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405046 | TTACTTGAAAGCAGC[A/G]AAAACAAGGCTACAG | 63893 |
| rs371145139 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435523 | CGCAATATTCCCCCC[A/G]TTTACTGCATGGGCT | 63893 |
| rs371152354 | snp | A/C/G | 0.000103475 | 0.00719226 | intron-variant | UBE2O | GRCh38.p7 | 17:76399041 | CCCCACCCCCTCCGC[A/C/G]GAAAGGGCAGAGAGT | 63893 |
| rs371165088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76421644 | TGCTAGGATTACAGG[C/T]GTGAGCCACCACGCC | 63893 |
| rs371269312 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405485 | GCTGCCCCCAGGCCC[A/G]GGGCTGGGGTGGGGA | 63893 |
| rs371273433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76445439 | CCCCCAACCAAAGAA[C/T]CAGATTAAACCCAAA | 63893 |
| rs371287586 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418903 | TTGTTTATCAGCTTG[A/G]AAAACACGGATTTTT | 63893 |
| rs371289958 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | UBE2O | GRCh38.p7 | 17:76400305 | GCTTCACCCTGGTTG[C/G]GGAAGAAGTGGGGGT | 63893 |
| rs371315298 | snp | C/T | 4.9652e-05 | 0.00498232 | missense | UBE2O | GRCh38.p7 | 17:76391026 | CCCGGATGCTCTTGA[C/T]GAAACCCTTGGAAAG | 63893 |
| rs371343659 | in-del | -/CTGTGA/GT/TG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415796 | CAACAGAGCAAGACT[-/CTGTGA/GT/TG]GTGTGTGTGTGTGTG | 63893 |
| rs371387784 | snp | C/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390345 | GCAAGTTCAACAGGC[C/T]TGAGGGCTATAACGT | 63893 |
| rs371423844 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416603 | CTCCCTGAGCCCACA[C/T]CAACCTCCCCGCGCT | 63893 |
| rs371463239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76392867 | CTGAGGTGGGAGAAT[C/T]GCTTCAACCCGGAGG | 63893 |
| rs371501522 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | UBE2O | GRCh38.p7 | 17:76400098 | GCCATGGAAATGGCT[A/C]AAGGCCAGTTCCTCA | 63893 |
| rs371507668 | snp | A/G | 8.47738e-05 | 0.00650997 | intron-variant | UBE2O | GRCh38.p7 | 17:76401159 | AAGAAGAGACCCTGC[A/G]GGATGTGGGGCCAAA | 63893 |
| rs371513273 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394671 | AAAAGTATAAAAAAA[-/A]GGTCATCCGTTTGGA | 63893 |
| rs371519187 | snp | A/T | 0.000236195 | 0.0108647 | intron-variant | UBE2O | GRCh38.p7 | 17:76405500 | GGGGCTGGGGTGGGG[A/T]CGCAGGACTCACGGT | 63893 |
| rs371521687 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421595 | GTCTTGAACTTCCGA[A/C]CTCAGGTGATCCGCC | 63893 |
| rs371531547 | snp | C/G | 1.65272e-05 | 0.0028746 | missense | UBE2O | GRCh38.p7 | 17:76397823 | GATGATGGTCTTTGA[C/G]TTGTCAGCCCACACC | 63893 |
| rs371549024 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436230 | CCAGCCTGGGCAACA[A/C]GAGCAAACTCCATCT | 63893 |
| rs371550905 | snp | C/T | 5.04113e-05 | 0.00502027 | missense | UBE2O | GRCh38.p7 | 17:76390992 | TCTAGCAGGGCAGCC[C/T]GGAACTGCGTCAGGA | 63893 |
| rs371604644 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76401975 | AGGAAACCGCTCTGT[A/T]TAGCTGGGTCCAGGT | 63893 |
| rs371614426 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBE2O | GRCh38.p7 | 17:76401202 | TGAGCGGTGTCTCCA[C/T]GGGTGACCATGCTCT | 63893 |
| rs371627144 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416846 | CAGTGAAACAGGACT[C/T]AAATACTAACTAGAA | 63893 |
| rs371636783 | snp | A/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389985 | GGCCTGTCTCTGGGC[A/T]CTAGGAGAGCCCCCG | 63893 |
| rs371735191 | in-del | -/AATAAAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423726 | ATAAATAAATAAATA[-/AATAAAT]AAAAATAAGGTCAGG | 63893 |
| rs371769625 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76397235 | GACATGTAGAAGGGC[C/T]GACATATCCTGCTGC | 63893 |
| rs371771176 | in-del | -/GAGA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433734 | AAAAAAAGAGAGAGA[-/GAGA]TGGGGTTTCGGCCAG | 63893 |
| rs371797000 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76410375 | GTGGTCATAAAGGGT[A/G]GTGGGGGTTCTGGTA | 63893 |
| rs371801297 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426908 | AGGTCTCTTAGTAAA[C/T]ACAACTTTTTTTTTT | 63893 |
| rs371859513 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455067 | GGGGAGTGGAGGTTG[C/T]AGTGAGCCTAGATCG | 63893 |
| rs371894501 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | UBE2O | GRCh38.p7 | 17:76402732 | AGGGGCAGTGAGACA[C/T]AGCAGACAACGTTCA | 63893 |
| rs372007033 | snp | A/C | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390236 | TTGCTTTCCCTGCAG[A/C]TCCCTGGTCCTCAAC | 63893 |
| rs372011070 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423596 | TACTTGGGGGGCTGA[A/G]GCAGGAAAATCGCTT | 63893 |
| rs372034469 | snp | A/C/G | 3.34176e-05 | 0.00408753 | intron-variant | UBE2O | GRCh38.p7 | 17:76399008 | TGCGGGTGCAGGCCA[A/C/G]TCAGCAGGCCATGCA | 63893 |
| rs372055745 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431045 | AGGTGCTTGATCTTT[A/C]GTTCTGTGAAATTCC | 63893 |
| rs372106023 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433289 | AAGTACTGATACATG[C/T]TACAACATGGATGAA | 63893 |
| rs372109904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432977 | ACCCACCAACATTGC[C/T]GGTGGGTATGTAAAA | 63893 |
| rs372258675 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76406172 | CCTCAGGATGGTTGG[C/G]TCTTGGAGCCCGGCC | 63893 |
| rs372266259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406860 | ACGTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 63893 |
| rs372284263 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438388 | ACTTAAAGGCTCCTC[A/G]TCGCTCTTCTGATCA | 63893 |
| rs372317090 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405889 | CACATAAGGCTGCAC[A/T]TTAATGAAGGATTTA | 63893 |
| rs372330416 | snp | A/G | 9.89511e-05 | 0.00703319 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398862 | TACCACGAAGTCTCC[A/G]GGGCAGAACTCGTTG | 63893 |
| rs372379940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76404687 | TTGGAAAACACACAA[A/G]AGGTGTGTGTATTCC | 63893 |
| rs372402688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434705 | AAACTAAGCAATTCC[A/G]ACATGGCAAAGGTCA | 63893 |
| rs372452472 | in-del | -/ACAC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435418 | CACACACACACACAT[-/ACAC]ACACACACACACACA | 63893 |
| rs372466589 | snp | C/G/T | 2.15692e-05 | 0.00328392 | intron-variant | UBE2O | GRCh38.p7 | 17:76400561 | TGCACCTGGGGATGG[C/G/T]AGGTGGGACACGCCA | 63893 |
| rs372550691 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417466 | ATTTTAGATACACCA[G/T]GAGAGCTATCTGAAG | 63893 |
| rs372570552 | snp | A/T | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451450 | TGTGGATGTATGTGC[A/T]TCCCCAACAAAAAGA | 63893 |
| rs372642735 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76399374 | GTGCGAGCGCAGGCA[C/T]GCACACCGAGGGGAC | 63893 |
| rs372648373 | snp | A/G | 1.67981e-05 | 0.00289806 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391297 | GGAGTCTGACAGCTC[A/G]GCTACAGCTGGGGGC | 63893 |
| rs372651010 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416093 | TACATATGTACATAC[A/G]TGTATATGCGTATGT | 63893 |
| rs372665160 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76448873 | CTGGTGATGGGGAAG[C/G]GGCAAGCCTCCTCTA | 63893 |
| rs372712711 | snp | A/G | 0.000549543 | 0.0165671 | intron-variant | UBE2O | GRCh38.p7 | 17:76400403 | AGAGCCCTGTCCCAC[A/G]CGTGCCCCTGGGTTG | 63893 |
| rs372835090 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422559 | AGTCCTGCAGGTGTC[C/T]GAGCAGGACGGAGGT | 63893 |
| rs372928726 | snp | A/G/T | 0.000149725 | 0.00865112 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405236 | GTCCTTGCTGTTGAC[A/G/T]GGATAGATGATGCAG | 63893 |
| rs372937922 | snp | C/G | 0.000153988 | 0.00877328 | missense | UBE2O | GRCh38.p7 | 17:76398383 | CCTCTTCTCCAATCA[C/G]CTGTGGCACAGGACA | 63893 |
| rs372959759 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76444375 | CCAATACCATGGTGA[A/G]ACCCTGTTTCTACAA | 63893 |
| rs372960676 | in-del | -/GGAAAGAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417708 | CCTTCGACTACAGGA[-/GGAAAGAA]TGCTAAGCATGTCCA | 63893 |
| rs372973421 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445574 | TCAGGAGAACACAGC[C/T]TACCTGTGTCTAGGG | 63893 |
| rs373028762 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421340 | AAAGACACTAGAGCA[C/T]GGAACATAATTTGAG | 63893 |
| rs373042754 | snp | C/T | 4.94189e-05 | 0.00497062 | missense | UBE2O | GRCh38.p7 | 17:76399558 | GACTCGTGCCGCTGC[C/T]GCTCTGGGAGGAAGT | 63893 |
| rs373070715 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427921 | CAAATCCAAACCTCT[A/G]TTATTGTTAGGGTCG | 63893 |
| rs373073174 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401836 | AGCCGAGATCGCACC[A/G]TTGCACTCCAGCCTG | 63893 |
| rs373148547 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411327 | CTACTTTCAAGTGAT[G/T]TTGATTGTCATGTCC | 63893 |
| rs373170036 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420866 | CAGTGAGTTGGCAGG[A/G]ACGGCCTTGTCACTC | 63893 |
| rs373306096 | snp | A/G | 3.29587e-05 | 0.00405934 | missense | UBE2O | GRCh38.p7 | 17:76399773 | GCAGAGCCATCGGGC[A/G]TCTCCTCAGGGCTGG | 63893 |
| rs373380516 | snp | A/G | 1.65236e-05 | 0.00287429 | intron-variant | UBE2O | GRCh38.p7 | 17:76398213 | TGCAGCTGGTGCACA[A/G]GGCAGTGAGCAGCCA | 63893 |
| rs373403612 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424266 | CAGCCTGGAGTGCAA[C/T]GGCACAACCTAGGCT | 63893 |
| rs373417537 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE2O | GRCh38.p7 | 17:76404987 | CACTGGCAGCCTATG[C/T]TGGGGTTGGGGAAGG | 63893 |
| rs373424474 | snp | A/G | 0.000266658 | 0.0115437 | intron-variant | UBE2O | GRCh38.p7 | 17:76405506 | GGGGTGGGGACGCAG[A/G]ACTCACGGTGGATCG | 63893 |
| rs373478803 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415950 | GTATGCGTATACATA[C/T]GCACATACACGTATA | 63893 |
| rs373499618 | snp | A/G | 4.98815e-05 | 0.00499382 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396183 | GCTGGTGAAGGTGAC[A/G]CCAGGCTTGCCGCCA | 63893 |
| rs373516733 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439090 | CACACACAGCAAGCA[C/T]GACACCAGTGGCCTT | 63893 |
| rs373522679 | in-del | -/ACTTA | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453965 | TAGGCACACTGATTA[-/ACTTA]TTTTCATCTTAATTT | 63893 |
| rs373569493 | in-del | -/TTTA | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76422759 | TCTCTATCCACCTGC[-/TTTA]TTTTTCTTCACAGCA | 63893 |
| rs373582548 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396228 | CACCGGGGTTTCGCT[A/G]GGCCACTCAGCCTTC | 63893 |
| rs373607363 | snp | C/G | 5.15389e-05 | 0.0050761 | intron-variant | UBE2O | GRCh38.p7 | 17:76401180 | TGGGGCCAAAGGAAA[C/G]TCCCCGTGAGCGGTG | 63893 |
| rs373668112 | snp | C/T | 0.000254231 | 0.0112717 | intron-variant | UBE2O | GRCh38.p7 | 17:76391880 | GTGGCTCTTCCTCCT[C/T]CTTGGCTGGGGGCCT | 63893 |
| rs373720636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408181 | TCCTCTCCCTGCCCC[C/T]GTATGCACAACCTGC | 63893 |
| rs373727300 | snp | C/T | 6.59033e-05 | 0.00573997 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396381 | GATGTCATCCAGAAA[C/T]TTCTTCTCCCGAGTT | 63893 |
| rs373770714 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399360 | ATGCAGAGGTGTGTG[C/T]GCGAGCGCAGGCACG | 63893 |
| rs373789259 | snp | A/G/T | 0.000183306 | 0.0095719 | intron-variant | UBE2O | GRCh38.p7 | 17:76400315 | GGTTGGGGAAGAAGT[A/G/T]GGGGTGAGCTGGGCT | 63893 |
| rs373819270 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408557 | AAGACTTCTGGCAGG[C/T]CTACACATTTAAAGA | 63893 |
| rs373849213 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411486 | AAAAGGGGAGCTGGA[A/G]GAAGTCCAAAAGCAG | 63893 |
| rs373851595 | snp | A/G | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390869 | GGCATGGGAAGAGGG[A/G]TGATTCCGGGGGGGA | 63893 |
| rs373907725 | snp | C/T | 0.000193981 | 0.00984647 | intron-variant | UBE2O | GRCh38.p7 | 17:76391704 | GACTATCAGAGTCAC[C/T]TTCCTCCACCGGCCC | 63893 |
| rs373949750 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394601 | ATACAAAATATTATG[C/T]ACTTATGGTGATACA | 63893 |
| rs373951372 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425695 | ACAGCTGAACCAAGT[G/T]GTGTTCCGTGTCCTC | 63893 |
| rs373953466 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413562 | TCAGTTGCATATATA[A/C]CACGTATGTGTCCCG | 63893 |
| rs373977188 | snp | C/T | 0.000101008 | 0.00710591 | intron-variant | UBE2O | GRCh38.p7 | 17:76400988 | TCAAGGACTCCATCT[C/T]CTACCCTTGGGCCCG | 63893 |
| rs373984461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76398199 | GCAGCATCAGGGACT[A/G]CAGCTGGTGCACAGG | 63893 |
| rs374072444 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391537 | GTAACAGCGACTGTT[C/T]TCATAGCCTTCCTGC | 63893 |
| rs374073452 | snp | A/G | 0.00013967 | 0.00835556 | intron-variant | UBE2O | GRCh38.p7 | 17:76402160 | GGTTTGGTCTCCACC[A/G]GGGGACACAGTGAGT | 63893 |
| rs374117717 | snp | C/T | 3.29696e-05 | 0.00406001 | missense | UBE2O | GRCh38.p7 | 17:76398531 | TGCAGGTACGGCCGA[C/T]GTGGTCCCCAGACTG | 63893 |
| rs374130898 | in-del | -/CAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433191 | AAAATGACACAACAA[-/CAA]ATGTCCATCAACTAA | 63893 |
| rs374156280 | snp | C/T | 3.43141e-05 | 0.00414197 | missense | UBE2O | GRCh38.p7 | 17:76400456 | CTGCCTAGGTTTTCC[C/T]GGGTGATGACAGAGG | 63893 |
| rs374180409 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449168 | GTAAATTTGTTCACT[A/G]AAAACTTGAGACTAA | 63893 |
| rs374182519 | snp | C/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390062 | TGACAGTAGGCCTTC[C/T]AGTCCAAGAGAGGGC | 63893 |
| rs374257751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411986 | CTGTGCCTGGCCCCA[A/G]TACTAGGTTTTCAGC | 63893 |
| rs374290854 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426964 | CCCATTATTGAACGA[C/T]AATTTAAGCTGGTTG | 63893 |
| rs374402352 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405152 | CCCAGAGGTCGTGCC[A/G]CCGAGAGAACCAGAG | 63893 |
| rs374408473 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435628 | AGCCCTCTCGAAGGT[C/G]ATCTCGTGCAATCCC | 63893 |
| rs374430472 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413667 | TCTGCCCAGCACCTG[C/T]GCCGACTCTCGGTCC | 63893 |
| rs374498059 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | UBE2O | GRCh38.p7 | 17:76417006 | CAGGGACCAGGTCCT[-/G]CAGGGGCCACAGAGT | 63893 |
| rs374509574 | snp | A/G | 1.7119e-05 | 0.00292562 | intron-variant | UBE2O | GRCh38.p7 | 17:76399420 | CTTCACGCTGACGCC[A/G]TTGGGGAGGGGCACA | 63893 |
| rs374536958 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449780 | AAAAAATTAGCCGGG[C/T]GTGATGGCGTATGCC | 63893 |
| rs374586900 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76404395 | GGGCATGAGGCAACA[A/C]CAGGAAGACCCAGGC | 63893 |
| rs374688537 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392267 | GATGCCACCAGCAGT[A/G]GAGAAGCTAAGGACA | 63893 |
| rs374692975 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | UBE2O | GRCh38.p7 | 17:76400206 | GACATTCCCAGGCAA[C/T]CTTGGCTGGCTCTAC | 63893 |
| rs374702723 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405655 | GCTTCTGAAGGAAAG[C/T]GTCACATCCACACTG | 63893 |
| rs374708728 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419802 | TGGCCCTGAGAACCC[A/G]ATGCTCAGAGCTGTG | 63893 |
| rs374829321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395636 | GGTGCCAGTCAGCCC[C/T]GGAGGTTTGGGGACC | 63893 |
| rs374833812 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76427102 | GGGGAGTAATCTGCC[C/T]TTCTTCTCAAGCTGC | 63893 |
| rs374950260 | snp | C/T | 1.65343e-05 | 0.00287521 | missense | UBE2O | GRCh38.p7 | 17:76397840 | TGTCAGCCCACACCA[C/T]CTCCACCTTGCTGCT | 63893 |
| rs374962765 | in-del | -/TTAAC | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453962 | AAATAGGCACACTGA[-/TTAAC]TTATTTTCATCTTAA | 63893 |
| rs374964908 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444278 | GGTCAGCTAGGCACC[A/G]TGGCTCACGTCTGTA | 63893 |
| rs375011301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410189 | AAGATGGAAGCCCCT[A/G]AAGGCCTCCACTCAG | 63893 |
| rs375028778 | snp | C/T | 3.31466e-05 | 0.0040709 | missense | UBE2O | GRCh38.p7 | 17:76396703 | TCCTCCACCAGCCCA[C/T]TGTCCGTCTCCCAGC | 63893 |
| rs375065665 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441986 | CCAATAGAGAGCCTC[A/G]TTCGTACTTAGCCAT | 63893 |
| rs375071440 | in-del | -/CAAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444230 | ATCTCACAAACAAAG[-/CAAAA]CAAAACAAAACAAAA | 63893 |
| rs375146547 | snp | C/T | 8.88123e-05 | 0.0066632 | intron-variant | UBE2O | GRCh38.p7 | 17:76400399 | GCCCAGAGCCCTGTC[C/T]CACGCGTGCCCCTGG | 63893 |
| rs375168133 | snp | A/C | 0.000214138 | 0.0103452 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399571 | GCCGCTCTGGGAGGA[A/C]GTGGTGGAGCTGGCA | 63893 |
| rs375168376 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76406823 | TCCCGTCTCAACCTC[A/C]CGAGTAGGTGGGACT | 63893 |
| rs375228819 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76414156 | GGGAGGGGAGGGAGA[A/C]CCTCCGGAAATGGCT | 63893 |
| rs375244216 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421293 | ATGGTCACCATTCTT[C/G]CAGATACTGAAACAC | 63893 |
| rs375245770 | snp | A/C | 1.69006e-05 | 0.00290689 | missense | UBE2O | GRCh38.p7 | 17:76401154 | CATCGAAGAAGAGAC[A/C]CTGCGGGATGTGGGG | 63893 |
| rs375247499 | snp | C/T | 0.000207076 | 0.0101733 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390913 | GGCTGGCCTCTCCCA[C/T]GGTGATGCTCTTTCC | 63893 |
| rs375251859 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399315 | GCACCTACGTTGTCT[C/T]GGGTGGGAGCCCCGG | 63893 |
| rs375258046 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425613 | CCTTTGCCTGTACTC[C/T]ATCCTTTCAACAGTT | 63893 |
| rs375303509 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431923 | TGGATTGCTGTGATC[A/T]AACCATGACAGTCAG | 63893 |
| rs375354678 | snp | C/T | | | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399892 | GCATGACATGATCCG[C/T]ACAACCTGCTTCTTC | 63893 |
| rs375363695 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394954 | GATCTTGGCTCACTA[C/T]AACCTCTGCCTCCCA | 63893 |
| rs375368940 | snp | C/T | 0.000206132 | 0.0101501 | intron-variant | UBE2O | GRCh38.p7 | 17:76399416 | CTGGCTTCACGCTGA[C/T]GCCATTGGGGAGGGG | 63893 |
| rs375374825 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390286 | GCCACCACCTCTCCT[A/G]GGCGTCACCCGGAAC | 63893 |
| rs375378883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76423642 | AGCTTGCAGTGAGCC[A/G]AGATCACAACACTGC | 63893 |
| rs375380912 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409811 | AACACAGTTGCCCTC[C/T]GAGGAGAGGGATTCT | 63893 |
| rs375434012 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE2O | GRCh38.p7 | 17:76400401 | CCAGAGCCCTGTCCC[A/G]CGCGTGCCCCTGGGT | 63893 |
| rs375469255 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433152 | AATGCTTATAGCAGC[A/G]TTATTCAGAATAGCC | 63893 |
| rs375471685 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430653 | TTATTGATTTTGCCA[A/C/T]GGCCATGCTTGTAGA | 63893 |
| rs375519843 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76397744 | CACGCCTGTGGCCCC[C/T]GGCCCAAGTTGCCAT | 63893 |
| rs375540388 | snp | A/G | 0.00019998 | 0.00999749 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452740 | CTTGGTCTCCTTCAC[A/G]TGCTGCTTGACGCCC | 63893 |
| rs375662538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425019 | GGGACTACAGGCACC[C/T]GCCACCACGCCCAGC | 63893 |
| rs375708844 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414394 | GAGGTAAGATGAAAT[C/T]ACACCTGAAAACAGT | 63893 |
| rs375726164 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434936 | TAGAGGGGCTCGGGC[A/G]CGCCCATCCAGGGAT | 63893 |
| rs375726548 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405935 | GAGAGCAAAACATTT[A/G]CTTTGCGTTCAATCT | 63893 |
| rs375729911 | snp | C/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452101 | TCAGAATCCTCCCCC[C/G]CAAGTACTATTCATA | 63893 |
| rs375747340 | snp | C/T | 1.68929e-05 | 0.00290623 | intron-variant | UBE2O | GRCh38.p7 | 17:76398806 | TCATTGGCGACCACC[C/T]TGCTGGCTGCCCTTC | 63893 |
| rs375760688 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414162 | GGAGGGAGAACCTCC[A/G]GAAATGGCTGGAAGT | 63893 |
| rs375831833 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448883 | GGAAGGGGCAAGCCT[C/G]CTCTAAGGAGATCCA | 63893 |
| rs375855569 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449220 | CCTCCAATTTACAGA[A/G]AAAACTACAAAAATA | 63893 |
| rs375915007 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411863 | AATTTTATTTTTTTT[-/T]GTAGAGACTGGGTTT | 63893 |
| rs376043748 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | UBE2O | GRCh38.p7 | 17:76405481 | GGTGGCTGCCCCCAG[A/G]CCCGGGGCTGGGGTG | 63893 |
| rs376102165 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412825 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 63893 |
| rs376201036 | snp | C/G/T | 8.23885e-05 | 0.00641781 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398475 | GGCTGCACACACCTC[C/G/T]ACGTCGTCCCCACTC | 63893 |
| rs376313758 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394063 | CAACCCAAGAAAAAA[-/A]CCAAAAGCGTTATTA | 63893 |
| rs376362212 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBE2O | GRCh38.p7 | 17:76398238 | CAGCCATCCAGAACT[C/T]GAATTTGAAGGCGTA | 63893 |
| rs376413640 | in-del | -/A/AAA | 0.439363 | 0.163222 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454322 | CTACTAAAAATACGG[-/A/AAA]AAAAAAAAAAAAAAT | 63893 |
| rs376500825 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420235 | TTTTTAAAAATGCAA[A/C]TATGGTAGGAAAAGG | 63893 |
| rs376532912 | snp | C/G/T | 6.62048e-05 | 0.00575314 | intron-variant | UBE2O | GRCh38.p7 | 17:76391737 | CCTTGTCCGCACCCC[C/G/T]GCTTCAGCCCAACTG | 63893 |
| rs376566042 | snp | C/T | 6.62405e-05 | 0.00575464 | missense | UBE2O | GRCh38.p7 | 17:76405271 | TGCCGATGAGCTTGA[C/T]GGCACAGTCGATGTT | 63893 |
| rs376589354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405007 | GTTGGGGAAGGGCAC[A/G]TCCTGACCTCATGTC | 63893 |
| rs376597762 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435520 | ATTCGCAATATTCCC[C/G]CCGTTTACTGCATGG | 63893 |
| rs376636790 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76402263 | AACTCAGCCCGAGGT[A/G]GTACAAGAAACTCTC | 63893 |
| rs376705308 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418553 | GCCTCCACAGGTCCC[C/T]TGGAAGGAGGAACAG | 63893 |
| rs376734404 | snp | A/C | 0.000101138 | 0.00711046 | missense | UBE2O | GRCh38.p7 | 17:76390990 | CCTCTAGCAGGGCAG[A/C]CCGGAACTGCGTCAG | 63893 |
| rs376767198 | snp | A/G/T | 9.92847e-05 | 0.00704517 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396195 | GACGCCAGGCTTGCC[A/G/T]CCACACTGCTGGCAC | 63893 |
| rs376776215 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416236 | TATGTATATGTGTAT[A/G]TATGTGTGTATATGT | 63893 |
| rs376813113 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428835 | CCTGATTTTCATATT[A/G]TCTGTGATTATATAA | 63893 |
| rs376814313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415314 | ACCCTATGACCCCCA[C/T]GAAGGAGGCACCACT | 63893 |
| rs376889823 | snp | A/C/T | 6.77568e-05 | 0.00582018 | intron-variant | UBE2O | GRCh38.p7 | 17:76401158 | GAAGAAGAGACCCTG[A/C/T]GGGATGTGGGGCCAA | 63893 |
| rs376904746 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424809 | GGCAACAGAGCAAGA[A/C]TCCATCCACCTCTAC | 63893 |
| rs376906577 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76451166 | CGTTCCAAAAATCAC[G/T]AATCTCTCAAATAGA | 63893 |
| rs376966817 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439529 | TCACTGCTCTGATGG[C/G]CAATAGAATGTATGC | 63893 |
| rs376974866 | snp | A/G | 3.2956e-05 | 0.00405918 | missense | UBE2O | GRCh38.p7 | 17:76399717 | GCTCTCCTGCCTCGT[A/G]GGGCTCCTCTGCACC | 63893 |
| rs377100110 | in-del | -/AGTTCTAGGCTGCATCCCA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76402871 | CAGGCCCTCCCTACA[-/AGTTCTAGGCTGCATCCCA]GCTGCTCTTCCCAGT | 63893 |
| rs377282089 | snp | C/T | 3.306e-05 | 0.00406558 | intron-variant | UBE2O | GRCh38.p7 | 17:76397796 | GTCTTGCCAGAGCCT[C/T]ACCTGGGGCAGGATG | 63893 |
| rs377295538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76406521 | GGAGAACTGAGTCGC[C/T]GAAAAAGGAAGATAC | 63893 |
| rs377315336 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439041 | ATGTAAAAAACAAAT[C/T]CCAACTCCTGAGTCA | 63893 |
| rs377405687 | snp | C/T | 0.000207652 | 0.0101874 | intron-variant | UBE2O | GRCh38.p7 | 17:76405606 | GTGTGAGAGAATGGA[C/T]TCTGAAGCCACCACA | 63893 |
| rs377453162 | snp | C/G | 0.000153988 | 0.00877328 | missense | UBE2O | GRCh38.p7 | 17:76391242 | AGCCCTGGGAGGCCT[C/G]TCCTGGGGCTGGCCC | 63893 |
| rs377494770 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394938 | TGGAGTGCAATGGTG[C/T]GATCTTGGCTCACTA | 63893 |
| rs377512923 | snp | C/T | 0.000131848 | 0.00811828 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399796 | AGGGCTGGCAGACTC[C/T]GCTTCGCTCTTGGTT | 63893 |
| rs377615515 | snp | C/T | 0.000270961 | 0.0116365 | missense | UBE2O | GRCh38.p7 | 17:76396584 | CCACAGCCCCCTGGA[C/T]GGCAGCTGTGGCTGC | 63893 |
| rs377632119 | snp | A/G | 1.67441e-05 | 0.0028934 | intron-variant | UBE2O | GRCh38.p7 | 17:76401003 | CCTACCCTTGGGCCC[A/G]GACCCACCTCTTCCA | 63893 |
| rs377680283 | snp | C/T | 0.000218583 | 0.010452 | intron-variant | UBE2O | GRCh38.p7 | 17:76399972 | GTGCACCTGGGCAGG[C/T]CTGGCCCTAGGCATC | 63893 |
| rs377689096 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76418726 | AGGCACCCGCCACCA[C/T]GCCCGGCTAACTTTT | 63893 |
| rs377753174 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421819 | TTCCCATTTCTCCCA[G/T]CCTGGCTGGCTCTAT | 63893 |
| rs386799315 | multinucleotide-polymorphism | CAGAG/GCACC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434737 | GAGTGAAGTCGAAAG[CAGAG/GCACC]TGCGATGTTCTGGAA | 63893 |
| rs386799316 | in-del | AAC/CA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446462 | AAAAACAAAAACAAA[AAC/CA]AAAAAAAAAACCAAA | 63893 |
| rs386799317 | multinucleotide-polymorphism | AAC/CAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446462 | AAAAACAAAAACAAA[AAC/CAA]AAAAAAAAACCAAAC | 63893 |
| rs397714854 | in-del | -/A | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76395056 | ATTTTTGTATTTTTA[-/A]GTAGAGACAGGGTTT | 63893 |
| rs397726411 | in-del | -/ACTA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431656 | GGAAAAGAAAGACTA[-/ACTA]TTAGGGCCAGACACT | 63893 |
| rs397739307 | in-del | -/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76410771 | TCAGGCAGCCGTGGA[-/G]GGAGAGTGCTCCTGG | 63893 |
| rs397832924 | snp | A/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76435423 | tgtgtgtgtgtgtgt[A/G]tgtgtgtgtgtgtgt | 63893 |
| rs397951488 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431366 | AGATACAAAAAAAAA[-/A]TTAGCTGGGCGTGCT | 63893 |
| rs397969327 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450097 | AAAAAAAAAAAAAAA[-/A]TCTGCCACTACATTA | 63893 |
| rs398031643 | in-del | -/C | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76405327 | ACTTGCATGTCTCCT[-/C]CCCTCCCCCAGGACA | 63893 |
| rs398039142 | in-del | -/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76401895 | AGAAAGTATTAGAAC[-/T]TTTTTTTTTTTTTTT | 63893 |
| rs398041919 | in-del | -/G | 0.5 | 0 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389033 | AAAGAATGTGGCAGG[-/G]AAGGATCCATCCAAG | 63893 |
| rs398120026 | in-del | -/TTT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419135 | AGATTTTTTTTTTTT[-/TTT]AAATTAGGCCTGGTG | 63893 |
| rs527257739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449988 | CCCAGCTACCTGGGA[A/G]GCTGAGGCAGGAGGA | 63893 |
| rs527259607 | in-del | -/CACGCCATGCATGCATAGGT | 0.00676609 | 0.0577691 | intron-variant | UBE2O | GRCh38.p7 | 17:76438856 | GCACCTCTAGCACTC[-/CACGCCATGCATGCATAGGT]CACGCCATGCATGCA | 63893 |
| rs527281433 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441650 | ACTGGGAGTTTGTTA[C/G]ACACGCAGATTCTTC | 63893 |
| rs527293413 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416024 | GTATACATATGTACA[C/T]ACACGTATATATGTG | 63893 |
| rs527332984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444239 | AACAAAGCAAAACAA[A/C]ACAAAACAAAACAAA | 63893 |
| rs527380460 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | UBE2O | GRCh38.p7 | 17:76440328 | AATTTCATCTCTTTG[-/T]TTTTTTTTACTTTGA | 63893 |
| rs527440733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76401622 | GGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG | 63893 |
| rs527461499 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436277 | TATTAATTAATTAAC[A/G]AATAAAAGACTAGAA | 63893 |
| rs527520904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439108 | CACCAGTGGCCTTTC[C/T]AGGGGCAGCTGACGG | 63893 |
| rs527556177 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389434 | GGTGTGTGTGAGGGA[C/T]ACAAAGGCAACGGAG | 63893 |
| rs527582705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425666 | TAAATGTGTTATGAT[A/G]GAGGACAGAGCTCAC | 63893 |
| rs527591408 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390015 | GCCGGCCGTCCCCTT[C/T]GGATTGAGCCTGCAG | 63893 |
| rs527723200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437443 | CGACAGAGCGAGATT[C/G]CATCTCAAAAAAAAA | 63893 |
| rs527781513 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411962 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 63893 |
| rs527845982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76424257 | TTTGTTGCCCAGCCT[A/G]GAGTGCAATGGCACA | 63893 |
| rs527900782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418770 | GAGACAGGGTTTCAC[C/T]GTGTTGGCCAGGATG | 63893 |
| rs528021633 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | UBE2O | GRCh38.p7 | 17:76414520 | CAGGGGAACTGCACA[A/C]CAGGGACAGCCCCCA | 63893 |
| rs528035580 | in-del | -/GACC | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453416 | GCGAGAAGGGGCGGG[-/GACC]CGGGAGGAGGAAGTG | 63893 |
| rs528055432 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400076 | AAAGCACAGACTGTC[C/G]TTCTTGGCCATGGAA | 63893 |
| rs528129530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434541 | AAAAAAGGATTCCAA[A/G]CATGAATTAGGGTGA | 63893 |
| rs528144543 | snp | C/T | 3.40229e-05 | 0.00412435 | intron-variant | UBE2O | GRCh38.p7 | 17:76391641 | GACACCTTCCCTCAG[C/T]GGGTGAGAGAGGCCC | 63893 |
| rs528231663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421745 | TGGTAACTGATGCCT[G/T]GGGACTGCTGGCTGA | 63893 |
| rs528250805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76428755 | GTTACATGTGGTTAC[A/G]TGAATCCACAGATGT | 63893 |
| rs528296034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422191 | CCTCAATGGCTCCCA[A/G]CTATTTCAGTCACTC | 63893 |
| rs528308555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422315 | GCGGCTCACTTTAAC[C/T]TGGCTTTTCCCAGGC | 63893 |
| rs528411919 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453414 | GAGCGAGAAGGGGCG[A/G]GGACCCGGGAGGAGG | 63893 |
| rs528414242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410767 | CCTGCCAGGAGCACT[A/C]TCCCTCCACGGCTGC | 63893 |
| rs528435498 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76426227 | CAGGCTGGTCTCGAA[A/C/T]GGGGCTCAAGCGATC | 63893 |
| rs528570105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76421246 | GCAGAAAGAAGTGAC[A/G]GCCTGCTGTCAGCGC | 63893 |
| rs528579933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415575 | TTTGAGAGGGCAAGG[C/T]GGTTGGATCACTTGA | 63893 |
| rs528601986 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451396 | GCCTGATTCACATTT[A/C]TCTGAGGGGAAGCAG | 63893 |
| rs528638694 | snp | A/G | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390084 | AGAGAGGGCTGGCTC[A/G]CTTGGAGTTCAGTGA | 63893 |
| rs528676509 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392798 | TCTCTACTAAAAATA[C/T]AAAAATTAGCCAGGC | 63893 |
| rs528726825 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76446216 | TGGGTGAAAACCCAC[A/T]TGTCACAGAAAACCA | 63893 |
| rs528749456 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76403186 | CTAACAGAAAGGGAG[A/C]AGGAAGGAGAAGAAG | 63893 |
| rs528791480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446550 | AGAGGCCTCTAATGT[C/T]CTAAAGCAAAAACAC | 63893 |
| rs528827361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397234 | GGACATGTAGAAGGG[C/T]CGACATATCCTGCTG | 63893 |
| rs528900870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76424154 | ACCTTGTGATCCGTC[C/T]GTCTCGGCCTCCCAA | 63893 |
| rs528903652 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76417914 | GATGGTGCTGTTTCC[A/G]CTGGTATTTGAGTCC | 63893 |
| rs528911521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455081 | GTAGTGAGCCTAGAT[C/T]GCGCCGCTGCACTCC | 63893 |
| rs528963230 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76418434 | TCTGCACCCTGTGCT[A/G]GCCTCTGAAGGGCAA | 63893 |
| rs528980884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76412678 | ATAGTTCAAGACAGG[C/G]GTCACGTGTGTTAGT | 63893 |
| rs528998800 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76448700 | GGCTGAACTTGAACT[A/G]ACAGACAGCAGTCCT | 63893 |
| rs529045213 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76413457 | ACTGGACAAAAAAAA[A/C]CCTGAGTGCATTAAT | 63893 |
| rs529065883 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408742 | GCCGGCCTGGCAGGT[C/G]AACACTAGAGGGCAC | 63893 |
| rs529098485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449765 | CTCCACTAAAAATAC[A/C]AAAAATTAGCCGGGC | 63893 |
| rs529131065 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76443334 | CACTCTGTCGCCCAG[G/T]CTGGAGTGCCGGGGC | 63893 |
| rs529215123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76400935 | ACCCTCAAGAGCAGG[A/C]AGGAAAGGGGCAGCA | 63893 |
| rs529255002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447386 | CAGGGTTGTTGTGAG[C/T]GTGAAGTAAAACATC | 63893 |
| rs529256126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411732 | ACTCTGCCACCCAGG[C/T]TGGAGGGCAGTGGCG | 63893 |
| rs529278492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76404935 | ATTTTTTTAAAGAAA[C/T]GTTAGAGGAGAAAGG | 63893 |
| rs529325024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76398644 | CTAAGGAGCCCACAT[C/T]TCAAGCCAGTGCAGA | 63893 |
| rs529411177 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405957 | GTTCAATCTTTTTTC[C/T]GCCCTCTGCAAGTGC | 63893 |
| rs529416983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436064 | CTAGCCTGGGCAACA[C/T]GGCGAAAGCCTGTCT | 63893 |
| rs529447432 | snp | A/G | 6.58924e-05 | 0.0057395 | missense | UBE2O | GRCh38.p7 | 17:76399548 | CTCTTTTTGCGACTC[A/G]TGCCGCTGCCGCTCT | 63893 |
| rs529477484 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76429485 | AGGCAGAGGTTGCAG[C/T]GAGCCAAGATTACAC | 63893 |
| rs529491325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393071 | CAAAACCAACCTGGG[A/C]AACATAGTGGGACCC | 63893 |
| rs529537234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430002 | TCCCTATACAGACTG[C/T]CAACTAATCATAATC | 63893 |
| rs529560463 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76423183 | GTAGGTGAGGGGGTG[A/G]ATGTGGGCTGAGGAA | 63893 |
| rs529661489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444761 | GGGACCAGAGAAATG[C/T]TTTCTTCCTTGGCTT | 63893 |
| rs529678423 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76409180 | TCACCATATTAGCCA[C/T]GATGCTCTCGATCTC | 63893 |
| rs529686564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76416613 | CCACACCAACCTCCC[C/T]GCGCTTCTCAAACAC | 63893 |
| rs529713502 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421660 | GTGAGCCACCACGCC[C/T]GGCCCTGAGTGACTA | 63893 |
| rs529723558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438859 | ACCTCTAGCACTCCA[A/C]GCCATGCATGCATAG | 63893 |
| rs529760579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439138 | GCGTGGTTTGGAGGC[A/G]CTTGCCTGGCTTTAG | 63893 |
| rs529810390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76433355 | AGGCCACATCTAGTA[C/T]GCTTCCATTTATATG | 63893 |
| rs529826299 | in-del | -/CA | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389510 | GCTAATGAGCCAACA[-/CA]AAAAAAAAAAAAAAA | 63893 |
| rs529830144 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390242 | TCCCTGCAGCTCCCT[G/T]GTCCTCAACTCCATG | 63893 |
| rs529868941 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76439728 | CCTCTCTTGCCTTTA[G/T]GCGCACTGGACTTCC | 63893 |
| rs529872739 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76426292 | AGGCGTGAACCACCA[C/T]GCCCAGCCAAAAGAA | 63893 |
| rs529877208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76396954 | TTGGCAACCTCATTC[C/T]ACCCTTTCCCTGACC | 63893 |
| rs529934136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76427098 | ACCTGGGGAGTAATC[C/T]GCCTTTCTTCTCAAG | 63893 |
| rs529967560 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390761 | AAGCTCGCTTCAAAA[C/T]AGAAACGGCAGCATC | 63893 |
| rs530023877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76394907 | TTGAGATGAAGTCTC[A/G]CTCTGTTGCCCAGGC | 63893 |
| rs530171163 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76421086 | GGAAAGTGAACAGGA[-/C]TCAGCACCACCCATT | 63893 |
| rs530187848 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76450218 | TGGAATTCATAAGGA[G/T]CAGGAGGTGAGAAGA | 63893 |
| rs530235406 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438553 | CTTTGCGCCCCATCT[A/G]AGAAACCTTCTCCAA | 63893 |
| rs530252837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414537 | AGGGACAGCCCCCAC[A/G]CCCTCACCCCTGACA | 63893 |
| rs530274513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425462 | AATACTTTTTAATTT[C/T]TTAGCTGTTTGAATA | 63893 |
| rs530276024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419350 | TCTGACTACTTAGGA[A/C]TATTTGTCTTTAATT | 63893 |
| rs530325440 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447910 | CTGTCTGCTAATAAC[C/T]AAGTGGCCATCCTAG | 63893 |
| rs530424899 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450620 | CCTCAAAGTTGTTGT[A/G/T]TTTTTTTTCTTTTCT | 63893 |
| rs530473972 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76415427 | GCCTTTGTTTTGCTC[A/G]CCTGCCCTTCCTCAT | 63893 |
| rs530480649 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2O | GRCh38.p7 | 17:76435519 | AATTCGCAATATTCC[C/T]CCCGTTTACTGCATG | 63893 |
| rs530504102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76392419 | TACAGTGTGGGCCAC[C/T]GTGCCCAGATGATTT | 63893 |
| rs530537374 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2O | GRCh38.p7 | 17:76428897 | GTAGAGGGGACCCCT[C/T]TACTATTTTTTTTTT | 63893 |
| rs530588564 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424136 | GATGGTCTCGATCTC[C/T]TGACCTTGTGATCCG | 63893 |
| rs530599894 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76422404 | TCATAAGGTCTGGGC[A/C]CCCAGTGGCCTCTTC | 63893 |
| rs530626298 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426128 | TTACTTCAGCCTCCT[A/G]AGTAGCTGGGACTAC | 63893 |
| rs530741918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76400384 | AGGCATGTGACCAGG[A/G]CCCAGAGCCCTGTCC | 63893 |
| rs530761878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76412449 | GTCCTAGGTGTATAG[A/G]AAAAGAGTGAACTTG | 63893 |
| rs530764198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405397 | CCCAGGCAACCCCAG[C/T]GCACCCCCTGCAGAG | 63893 |
| rs530773887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421298 | CACCATTCTTCCAGA[C/T]ACTGAAACACTGGAG | 63893 |
| rs530820491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411785 | CAACCACCTGGGCTC[A/G]AGTAATCCTTCTGCC | 63893 |
| rs530829750 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76448017 | CATTGCAGAGGGAGA[A/C]AATGAGGCAGTGACT | 63893 |
| rs530859446 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452157 | TACTCACAAAGTTCC[C/T]TGCAGCAATTAAAAG | 63893 |
| rs530905658 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447046 | CTGCCTGCCCACTGG[A/C]ACAACTTCCACCTAT | 63893 |
| rs530919287 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452571 | GCTGCTGCAATGACT[C/T]TGCATGGAGTGTACC | 63893 |
| rs530994083 | snp | C/G | 0.000791814 | 0.0198816 | intron-variant | UBE2O | GRCh38.p7 | 17:76396041 | GGTCTGGCGAGGGGA[C/G]TAACCACCCTGCACC | 63893 |
| rs531040975 | snp | C/T | | | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400491 | GGGGCTGACGCTGTC[C/T]GTGCCCCCTGGACAG | 63893 |
| rs531041183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76447233 | TCCTGAACTTAAGTA[C/T]TCTCAGGTGAGAACA | 63893 |
| rs531042950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440472 | AGTTGGGACTACAGG[C/T]GTAAGCTGCCACGCT | 63893 |
| rs531063527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397724 | GAGAGCCCATCTTCT[A/G]GCTACACGCCTGTGG | 63893 |
| rs531102351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434650 | AGAGTCTTGCCTTGG[C/G]TTCTGCAAGGAGCTC | 63893 |
| rs531138680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403851 | AAGTTCTTAAAAAAC[C/G]AACAAAAAGGGCCAT | 63893 |
| rs531149304 | snp | C/T | 1.65941e-05 | 0.00288041 | intron-variant | UBE2O | GRCh38.p7 | 17:76391720 | TTCCTCCACCGGCCC[C/T]CCCTTGTCCGCACCC | 63893 |
| rs531160313 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397566 | CTGGAGGTTTGTGAA[A/G]GTCTACATGCACCCA | 63893 |
| rs531160618 | in-del | -/GCTCTCTTCACTTCCCCCTCC | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76441764 | AATCCATTTATTCAT[-/GCTCTCTTCACTTCCCCCTCC]CCCTCCACTGATAAA | 63893 |
| rs531209311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76419021 | TGCCACGGTGACTCG[C/T]GCTGTAATACCAGTA | 63893 |
| rs531245322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449281 | ATAGATACTACTAAA[A/C]AATTTCAATGGGGCA | 63893 |
| rs531303976 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436523 | CAGACTATTACACCT[A/G]GGACTTTCCCTCCTT | 63893 |
| rs531308161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449881 | GCCGAGCTGGCGCCA[C/T]TGCACTCCAGCCTGG | 63893 |
| rs531331658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407203 | GGTGCTCAGCAAGGT[C/T]GGCAGCTGTGATCAC | 63893 |
| rs531336962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413558 | CCGTTCAGTTGCATA[C/T]ATAACACGTATGTGT | 63893 |
| rs531398619 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76406621 | ACAAAAAAAAAAAGG[A/G]AAGAAAAGCAATGAA | 63893 |
| rs531430892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444626 | TCAGGGGAGCCGTCA[A/C]ACTCAGTGGTGTGAG | 63893 |
| rs531575120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76442048 | CATTCAGGAAACCCA[C/T]GTGTGTGGAATCTGC | 63893 |
| rs531587051 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76401570 | AGAAAAAAAAGCTAC[C/G]AAAAATGCAAATAAA | 63893 |
| rs531607230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395075 | GAGACAGGGTTTCAC[C/T]GGGTTGGTCAGGCTG | 63893 |
| rs531608103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76406011 | GGGAGAGTGGGCTGG[A/G]GGAGAAGCAGGACAC | 63893 |
| rs531622425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76431572 | CTTAGTTCAGACATT[C/T]ACCTACTCACCAATT | 63893 |
| rs531675474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395532 | AGGAAAGAAAGAACC[A/C]TCTGGCCTGGACACA | 63893 |
| rs531704942 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76448579 | GCACTATATCTCAAA[A/C]CTGGTGAAACCCTGA | 63893 |
| rs531746814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430049 | CAAACCTTATTCCCA[C/T]CTTGAGTGCCACCAA | 63893 |
| rs531789644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76393936 | CCAGGGAATGCACTA[C/T]TTTTCTTCTCCTGAG | 63893 |
| rs531801689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423806 | GATAGAGGTGGCCTA[C/T]GGCACAGTGTCCGCA | 63893 |
| rs531824451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76436720 | ACTTGACCCCTTGCC[C/T]TGACATCAAAAGCCA | 63893 |
| rs531855309 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412141 | GAGTGTGTAGACAAC[A/C]GGTCAGCTTGCAATG | 63893 |
| rs531911556 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454796 | CCACTACACTCCAGC[C/T]TTGGCAACAGAGCAG | 63893 |
| rs531963089 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76406607 | AAGAACGTGACTCAC[-/A]AAAAAAAAAAAGGAA | 63893 |
| rs531969509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403020 | TGGACACAGGACACC[C/T]GGCAAAGTAGGCTGT | 63893 |
| rs532014526 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76393360 | ACCTCTGCCTCCCAG[A/G]TTCAAGCGATTCTCT | 63893 |
| rs532018567 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76423965 | GTAGTGCTAGTGCAG[C/T]GGCGCGATCTTGGCT | 63893 |
| rs532157331 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397259 | CTGCTGCGTTCCCTG[C/G]AATGGCCGTTAAGGT | 63893 |
| rs532159708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76427163 | TCATACCACCATCCA[C/T]GTTTGTAATGTCTCT | 63893 |
| rs532229735 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76405006 | GGTTGGGGAAGGGCA[C/G/T]GTCCTGACCTCATGT | 63893 |
| rs532358244 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76432412 | TACCCAGCATGCCAC[A/G]GTACATGTGACTGGT | 63893 |
| rs532379988 | snp | A/T | 0.00119737 | 0.0244387 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389375 | AGGACCCACTGCCAC[A/T]TGCCTTCCCTGGCAA | 63893 |
| rs532484520 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418818 | TCGTGATCCACCCGC[A/G]TCGGCCTCCCAAAGT | 63893 |
| rs532535522 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428591 | CTGATTCCTCGGAGA[C/T]ACATTTTTCTCTTTG | 63893 |
| rs532568486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425623 | TACTCCATCCTTTCA[A/G]CAGTTCCACTGCATT | 63893 |
| rs532571455 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76445081 | GAGGAAGAACATCAT[C/T]GGAGCTGCTGAGTGT | 63893 |
| rs532597469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415530 | TGGCCCTGGGCCTGG[C/T]GAGGTGGCTCACACC | 63893 |
| rs532626675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420075 | TGATCCGGAGCCTCA[C/T]CCCTACCCAGCGCAG | 63893 |
| rs532632482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426130 | ACTTCAGCCTCCTGA[G/T]TAGCTGGGACTACAG | 63893 |
| rs532661123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408510 | TAACCAAATAAAAAG[C/T]TCATCTCTCCCCAGA | 63893 |
| rs532678351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414995 | TAAGTAGAAGGCAGA[A/G]AAGTGATCAGCATGA | 63893 |
| rs532692750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420603 | ATGATTCTCCACTCC[C/T]TACAACTCTGTAACT | 63893 |
| rs532693880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76402273 | GAGGTAGTACAAGAA[A/T]CTCTCCCACAACGAA | 63893 |
| rs532714607 | in-del | -/TTT | 0.0360663 | 0.129354 | cds-indel | UBE2O | GRCh38.p7 | 17:76389845 | ATCTTTGCTTTTGAG[-/TTT]TTTTTCCAACCTTAA | 63893 |
| rs532864700 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76425930 | CTGGATCCTGGGAAA[A/T]GTCCCTGGTTTTGGT | 63893 |
| rs532865654 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76409054 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 63893 |
| rs532892701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429433 | TGTAATCCCAGCTAC[G/T]TGGGAGGCTGAGGTG | 63893 |
| rs532900383 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454323 | CTACTAAAAATACGG[A/G]AAAAAAAAAAAAATA | 63893 |
| rs533037954 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76417237 | TCTTCACATGTGGGC[A/C]CCCCCATTGACCATC | 63893 |
| rs533088900 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76449044 | GAAGCCTCAGGAACA[C/G]GACAAATTCCATAGC | 63893 |
| rs533104181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76417871 | ACTGCACCTGCAGAA[C/T]TGGGCAGAAACTCCT | 63893 |
| rs533104734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76406453 | GCCAACCAGACACTC[C/T]TCCGTGGTGGCCTCT | 63893 |
| rs533148854 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452631 | CACTGCAGTGGCACC[A/G]CTCCGGGCAGGGCCC | 63893 |
| rs533157288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416259 | GTATATGTATGTATA[C/T]GTATATATATAAAGC | 63893 |
| rs533203441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446718 | AGCTCCTAATGGAGC[C/T]GACCACTTCTGAGGC | 63893 |
| rs533304139 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426351 | GGCTGGATACGGAAT[G/T]CTCTCAGAATGTTGC | 63893 |
| rs533313023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441422 | AGCACTGGCGGATGA[C/T]GAGTCCGCCTCATCC | 63893 |
| rs533323560 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449411 | AAACTGCCGTCTCTA[C/T]TAAAAATACAAAAAT | 63893 |
| rs533364618 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424722 | TCTACATAAAAAAAT[A/G]GCAGCAGGATCCCTT | 63893 |
| rs533373640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441989 | ATAGAGAGCCTCGTT[C/T]GTACTTAGCCATCCT | 63893 |
| rs533571482 | snp | C/T | 3.10429e-05 | 0.0039396 | intron-variant | UBE2O | GRCh38.p7 | 17:76400599 | CAGGCTCTGACAGCA[C/T]TCTCTTTAGCCAGCT | 63893 |
| rs533640058 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76392546 | CTGGGTTTACAGCCC[C/T]GAGCCGTCACTGTGC | 63893 |
| rs533641690 | snp | C/T | 1.65644e-05 | 0.00287783 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398979 | CATCGTGGTCACCAC[C/T]TCCACTGCCACCCTG | 63893 |
| rs533677066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393026 | ACTTTTGGGAGGCCA[A/G]GGTGGGAGGACTGCT | 63893 |
| rs533750084 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414523 | GGGAACTGCACACCA[C/G]GGACAGCCCCCACGC | 63893 |
| rs533778890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425151 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 63893 |
| rs533804677 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76423822 | GGCACAGTGTCCGCA[-/AAG]GAACCAGAACACAGG | 63893 |
| rs533838512 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434876 | GTTATAGTCCTTCCA[C/T]CTCCATCGGTGGTAC | 63893 |
| rs533898428 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407619 | ACCTAAATCAGTGCC[A/G]TCACTGATGAAACAC | 63893 |
| rs533899078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76431041 | ATTCAGGTGCTTGAT[C/G]TTTAGTTCTGTGAAA | 63893 |
| rs533917890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395153 | AGTGCTGGGATTACA[C/G]TCGTGAGCCACCGCA | 63893 |
| rs533972713 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76430107 | AGTGCTTTTCCTTGG[C/T]GTTTTTCCGCAGGTA | 63893 |
| rs534024929 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76417648 | ACTGAGCTGGGTCTT[A/T]AGAGGCCATCACTAA | 63893 |
| rs534030440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76423886 | CTCTCAGCTACTTCC[A/G]GGTTGGGTTCTTTTT | 63893 |
| rs534073844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419721 | ATCCCGCCAGCACGC[A/G]TCCTTGGGAACCTGG | 63893 |
| rs534082937 | in-del | -/TA | 0.00359352 | 0.0422356 | intron-variant | UBE2O | GRCh38.p7 | 17:76416004 | ATACACGTATATACG[-/TA]TGTGTATACATATGT | 63893 |
| rs534143189 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76413042 | AAAACAAAATGAAAC[A/T]AAAAAACCCAACTCA | 63893 |
| rs534145166 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76409291 | TTTCTTAGAGAGTCG[-/T]TAACTATCAGAGGTT | 63893 |
| rs534201143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413755 | GCTGGTCTTGGAACC[A/G]AAAAACATGCAAACC | 63893 |
| rs534231952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423393 | TCTAAAAAATAAATA[A/C]AGTAAAAATAAAAAT | 63893 |
| rs534243105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442994 | AGGTAAATTAAAAAT[G/T]ACCCCAAATGCTCTA | 63893 |
| rs534267690 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE2O | GRCh38.p7 | 17:76406684 | ATGGGAACTCATGAG[C/T]CCAAGTTGTTTTTTT | 63893 |
| rs534395867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455105 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGATTC | 63893 |
| rs534411060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415861 | TATACAAATATATAT[A/G]CATACATGTATATAC | 63893 |
| rs534463253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76448798 | GTCTAGCCAGTGCTC[A/G]TGAAGGTTTAAGTGG | 63893 |
| rs534468540 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76416001 | CACATACACGTATAT[A/G]CGTATGTGTATACAT | 63893 |
| rs534471447 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397237 | CATGTAGAAGGGCCG[A/C]CATATCCTGCTGCGT | 63893 |
| rs534483689 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419012 | ACTTCTGACTGCCAC[A/G]GTGACTCGCGCTGTA | 63893 |
| rs534499408 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440617 | ATAGCCATGAGCCAC[C/T]ATGCCTGGCCTCTAT | 63893 |
| rs534521314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394299 | CATAGTGCTTGGCTC[A/G]ATGCACAGGCCCAGT | 63893 |
| rs534540587 | snp | A/C/G | 3.30345e-05 | 0.00406403 | missense, intron-variant | UBE2O | GRCh38.p7 | 17:76400170 | CCATAGAGCCCTCCC[A/C/G]CTGGGCGCAGTTTTT | 63893 |
| rs534570468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446414 | AAGTAGTAAAAAATA[A/G]AAAAAGTTCCTCTTA | 63893 |
| rs534598292 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76403660 | TAATACATATGTATT[A/T]CCTAGTGTGTCCCAA | 63893 |
| rs534640260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397412 | GACCCAGCAGGTGGG[G/T]CTAGAACTGGGTCGG | 63893 |
| rs534651393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76427229 | TAACTAACTTCTGCA[C/G]ATCTGTTTTCCAGTT | 63893 |
| rs534761342 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76438957 | CCTCCAGGCTTCCTA[A/G]CTCCCCACATTCCAC | 63893 |
| rs534762688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76450734 | TCAAGCAATTCTCCC[A/G]CCTCAGCCTCCCGAG | 63893 |
| rs534777947 | snp | C/T | 1.65048e-05 | 0.00287265 | missense | UBE2O | GRCh38.p7 | 17:76391112 | CGGTAGCTCTTTCTC[C/T]GCTTCTTTGGTTTCA | 63893 |
| rs534791352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407878 | AGGGGCTCTTCTGAC[C/T]TTTCTATGACAAGGA | 63893 |
| rs534828278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444907 | AGAATCCCTGGAGAC[G/T]TATTTGTGTGTCTAC | 63893 |
| rs534852112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454272 | ACGAGGTCAAGAGAT[C/T]GAGACCATCCTGGCC | 63893 |
| rs534936905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76446972 | TCTGCAGAAGCACAC[C/T]GCCAGTGCGAATGCA | 63893 |
| rs534939939 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389700 | CCACGGTGTGTGGTC[A/C]GGCTCCATCCTCCCG | 63893 |
| rs534943122 | snp | A/C | 1.65825e-05 | 0.00287941 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396531 | TGGCCCGTCCTTGCC[A/C]GCCTTCTCCATCAGC | 63893 |
| rs534974997 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76420101 | CGCAGCAGTGGCCCC[C/G]TTCGCACCACACTCC | 63893 |
| rs535009898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450273 | GCAAGGTCCCAGGAC[C/T]CACCCTACCACCCTG | 63893 |
| rs535016862 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450083 | CAAACCAGTAACTCA[-/A]AAAAAAAAAAAAAAT | 63893 |
| rs535028022 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390381 | ACAGGCCATGTATAG[A/C]CGGGAGTCAGTGACA | 63893 |
| rs535038157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415053 | ACTGGGTATCACTAC[C/G]TAACCAGTGGCCCCG | 63893 |
| rs535039251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407413 | TTTGTGCTGCCCCAC[A/C]CTATCTTAATCCCCT | 63893 |
| rs535042532 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455163 | GGGCACAGTGGCTCA[C/T]GCCTGAAATCCCAAC | 63893 |
| rs535065268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454457 | GCCACTGCACTCCAC[C/T]CTGGGCAACAGAGCA | 63893 |
| rs535103852 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76401569 | GAGAAAAAAAAGCTA[-/C]CAAAAATGCAAATAA | 63893 |
| rs535172509 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431671 | ATTAGGGCCAGACAC[C/T]GTGGCTCACACCTGT | 63893 |
| rs535279024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432995 | TGGGTATGTAAAATG[C/G]TGCAGTTGCTTCAGA | 63893 |
| rs535281487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439392 | ATCCCTGAAACCCTT[C/T]CAGGAGGTCCAAAGT | 63893 |
| rs535305751 | snp | C/G | 1.79483e-05 | 0.00299564 | intron-variant | UBE2O | GRCh38.p7 | 17:76399940 | CAAGGGCGGAGCAGA[C/G]AGGACAGGGCTGTGA | 63893 |
| rs535343577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393667 | GGCCTGGGGAAGGGG[A/G]GATGGTCTCACAACC | 63893 |
| rs535345903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76433520 | ATAGCGGTGATGACC[A/G]TACAACCGTTTGAGT | 63893 |
| rs535379947 | snp | C/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452397 | TGGTGTAACGCCGAA[C/G]GCGCCCCAGAACCTG | 63893 |
| rs535400155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411346 | ATTGTCATGTCCCTG[C/T]AGGAGCGGATGGCTC | 63893 |
| rs535476543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448220 | ATCAAGGGACAAAGA[A/G]TAAAATCACAGAACA | 63893 |
| rs535528574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76405691 | TGCACAAATCCTAAG[C/T]GTTTGGCTAGCAGTA | 63893 |
| rs535554759 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393640 | AGCTGAAAGGCAGTT[C/T]CAGGCTGGTGAGGCC | 63893 |
| rs535561394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428505 | CTTTTTATTTCATGG[A/G]TAAAATATTGGCTCT | 63893 |
| rs535612613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436396 | TGCACTTTTGTATTA[A/C]GTATATAAATAACTT | 63893 |
| rs535623773 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76429047 | GCTGGGATTACGGGC[G/T]CATGCCACCATGCCC | 63893 |
| rs535645972 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76422144 | AAGTAACCCCAAAAT[A/G]CTAGTTCTCGTGGCC | 63893 |
| rs535676048 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76429814 | GGGATTTGCTCTTTT[A/T]GTGTGCAGACGTTCA | 63893 |
| rs535766425 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453629 | CAAAACAAATACACA[C/T]TAAATAGATAACAAA | 63893 |
| rs535838689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438279 | ATGGTTGCACAACAA[C/T]GGGAATGTACTTAAT | 63893 |
| rs535873039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76432098 | ATAAATAGCAGCACA[C/T]GTGCCCCTCAGCAGA | 63893 |
| rs535885412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395235 | CACCCAGGCTGGAGT[A/G]CAGTGGCGTGATCTC | 63893 |
| rs535932594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425222 | TTCTCAAGGTCCTTT[A/C]GACAAAAAAAAAAAA | 63893 |
| rs535949436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76436970 | AACCATTTCTACTAA[A/G]AATGCAAAACAAACA | 63893 |
| rs535997206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76392679 | GTATTCCAGCTGGGC[A/G]CGGTGGTTCGTGCCT | 63893 |
| rs536073449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420163 | AGCCACACTCTGAAA[A/G]TGCACCGTACCTTCC | 63893 |
| rs536133065 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76415099 | GATGCGACAGGCTGC[A/G]GTCCTGTGGCTGCCG | 63893 |
| rs536162790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76450923 | CCACACCCGGCCGTT[A/G]TTTTCGATTTAACTC | 63893 |
| rs536181042 | in-del | -/AGTG | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76423320 | GGAATTCGACGCTGC[-/AGTG]AGCCCTGATTGTGCC | 63893 |
| rs536206021 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76417984 | GCCTTGGGAGAAGTG[C/G]AGGTGGAGAAGTGGG | 63893 |
| rs536258136 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76444869 | TGCTTTCAGCACTGC[-/AT]ATGTCAAGCCCTGAG | 63893 |
| rs536286076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76424479 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAAC | 63893 |
| rs536293532 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431895 | TCAAATGTTAAAGAA[A/G]GTTTAAGTCCCATGG | 63893 |
| rs536303329 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389043 | GCAGGGAAGGATCCA[C/T]CCAAGTCTAAACTGG | 63893 |
| rs536345083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418820 | GTGATCCACCCGCGT[C/T]GGCCTCCCAAAGTGC | 63893 |
| rs536346394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413201 | TTTGCAAGAATCTGA[C/T]GTAGGGATGGGGTGG | 63893 |
| rs536390685 | snp | C/T | 0.00358779 | 0.0422022 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389496 | TGTCACCTTGTCTTG[C/T]TAATGAGCCAACACA | 63893 |
| rs536400525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419777 | ACTTCCAGGCAGGAA[G/T]GCCATGCTGTGGCCC | 63893 |
| rs536409667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413885 | ACAGTAAAACCAGGA[C/G]AGGCAGAAAATGGGG | 63893 |
| rs536471474 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441491 | CCGGTTCATTAACAC[C/T]GGCACTAGAAGAATA | 63893 |
| rs536533661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407311 | GGAGAGGCATGCTGG[C/T]GTGACGGTGCCACTT | 63893 |
| rs536544911 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76420738 | AGACGTCCTGGGATC[C/G]AGTGCAAGCTGGGGT | 63893 |
| rs536545520 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439017 | TAAACTCTGATGTAA[A/C/G]TCCTCTTTATGTAAA | 63893 |
| rs536570544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401226 | ATGCTCTCCACGCCT[C/G]TGCCCGCTGGCTGCC | 63893 |
| rs536580295 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76416040 | ACACGTATATATGTG[G/T]GTGTACATATGTACA | 63893 |
| rs536583399 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445973 | TCATGGGCAAGTGGA[A/G]CCTCAGGAAGGAGCT | 63893 |
| rs536660342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76416011 | TATATACGTATGTGT[A/G]TACATATGTACACAC | 63893 |
| rs536770609 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450036 | TCAAGGACACCTGAG[-/T]TAACAGTGAGACCCC | 63893 |
| rs536820847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449673 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCGAGG | 63893 |
| rs536854891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411059 | GGGGTGGGTGGGAAG[A/G]ACAGAGTTTCACTCT | 63893 |
| rs536892288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450028 | ACCAGGAATTCAAGG[A/C]CACCTGAGTAACAGT | 63893 |
| rs536892684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443716 | CAGCTGGGCATGTGA[C/T]GTCACTGTGGAAGTC | 63893 |
| rs536909261 | snp | A/C/G | 3.34181e-05 | 0.00408756 | intron-variant | UBE2O | GRCh38.p7 | 17:76397928 | AGGGGGCCCAGCTCA[A/C/G]GCTCCAGCTCCCCAG | 63893 |
| rs536929386 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408089 | ACCCCACCCATACTG[A/G]GCACTGGCTTTCTCC | 63893 |
| rs536940092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76400633 | CAAAGCCCACTTGAC[C/T]TCCAGAGCAGGAAAC | 63893 |
| rs536978551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394684 | AAAGGTCATCCGTTT[A/G]GAAGGAGACCCACTA | 63893 |
| rs536995783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421468 | CTTCCCCGGTTCAAG[C/G]GATTGTCCTGCCTCA | 63893 |
| rs537009746 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445370 | TCCTTTGACTTAGCT[A/G]CAGAATATTAAATAT | 63893 |
| rs537057600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421810 | GCCACGTGCTTCCCA[C/T]TTCTCCCATCCTGGC | 63893 |
| rs537127754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76416133 | TATACATATATGTGC[A/G]TGTATAGATATATAA | 63893 |
| rs537153762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439453 | TATTTGCCTTTTTTC[C/T]TCTCATCCTCTCCAA | 63893 |
| rs537167020 | snp | A/G | 0.000170984 | 0.00924461 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452992 | GCCGGCTTCTGGGCC[A/G]GAGTCCGAGGACGGC | 63893 |
| rs537219903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447041 | CCCTCCTGCCTGCCC[A/C]CTGGCACAACTTCCA | 63893 |
| rs537228095 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453491 | CAGGATGGTGGAGAG[A/G]CTGTCAACAACTTTT | 63893 |
| rs537260454 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390532 | GGACCAGGGGAATTG[C/T]TGGCGCAACCCACAC | 63893 |
| rs537282809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447505 | ATCTTTGTAATTTAT[A/G]ATCTCATTACCAGTC | 63893 |
| rs537330465 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449278 | TAAATAGATACTACT[A/G]AAAAATTTCAATGGG | 63893 |
| rs537353440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76441695 | AGGACAATTTGCATT[A/G]GGAGACCCTAGGTGA | 63893 |
| rs537371883 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76435239 | TATTTATGTAAAAAG[C/G]TAAAATATAAAAAAG | 63893 |
| rs537372447 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443290 | GTTGGGGAATATATA[C/T]ATATATTTTTTTCCT | 63893 |
| rs537424492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448764 | ACCATGACAGGTGGA[G/T]ACCAGAAGGACCCAC | 63893 |
| rs537466140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408781 | CTCTGGGAAAGCACC[A/G]GATTTGTGAACAAAA | 63893 |
| rs537486486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442895 | CAAGCAGAGAGCAAA[A/C]CAGGGTTGTGAAAGG | 63893 |
| rs537518945 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | UBE2O | GRCh38.p7 | 17:76432432 | TGTGACTGGTAAATA[-/T]TTTGAAAGCTTGCCC | 63893 |
| rs537546317 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410448 | CAGGACATCCCTCAA[C/T]GAAGAATGGCGTGGC | 63893 |
| rs537550649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443445 | AGGCACCCACCACCA[C/T]GCATGGCTAATTTTT | 63893 |
| rs537587745 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76394672 | AAAGTATAAAAAAAA[C/G]GTCATCCGTTTGGAA | 63893 |
| rs537590894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403423 | ACAGGCATGCATCAC[C/T]GTGCCTGGCCAATTT | 63893 |
| rs537607604 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76437564 | AGTGTATGGTTTAGA[C/T]AACAGTATGTGGCTG | 63893 |
| rs537618284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440003 | CTCCTAGCACCTACT[C/T]TGGGCCAGTCACTGA | 63893 |
| rs537665381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397262 | CTGCGTTCCCTGGAA[C/T]GGCCGTTAAGGTGAT | 63893 |
| rs537672138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426577 | TGAAAGCTTTAAACA[C/G]TATTTCTATTCTTTT | 63893 |
| rs537681905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76434191 | GAAATGACCCCGAGG[A/G]TCCCTTCCAGTCTTA | 63893 |
| rs537733710 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76427366 | TAATCCCTTTTAAGA[C/T]GTATTCTGTCTTATT | 63893 |
| rs537903969 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76393235 | TGCACTCCAGCCTGG[G/T]CGACAGAGTGAGACC | 63893 |
| rs537936419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422787 | ACAGCACTTACTGTT[C/T]CCACACCTGCAGTCT | 63893 |
| rs537995062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393779 | ATTTGCGTGCATCTG[G/T]GCACACACGCGTGTG | 63893 |
| rs538000583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423260 | GGTACGCACCTGGAG[C/T]CCCAGCTACTCAAGA | 63893 |
| rs538130927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76424665 | GGATTGCTTGAGGCC[A/G]GGAGTTCAAGACCAG | 63893 |
| rs538133296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418038 | CCACCTCAGGAGGAA[A/G]GCGCAGGGGGAGGTC | 63893 |
| rs538180954 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455087 | AGCCTAGATCGCGCC[A/G]CTGCACTCCAGCCTG | 63893 |
| rs538196825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76412964 | AGTGAGCCGAGATTG[C/T]GCCATTGCACTCCAG | 63893 |
| rs538224945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76392735 | AGACGGGTGGATCAC[C/T]TAAGGTCAGGAGTTC | 63893 |
| rs538273754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76425889 | CAGACTTTCCTCTGC[C/T]GCTCACCTGTGTCAG | 63893 |
| rs538402270 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76420858 | GCTGACCCCAGTGAG[C/T]TGGCAGGGACGGCCT | 63893 |
| rs538447575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76417489 | ATCTGAAGAGAACCA[A/G]CAGGAAATCTTAGAG | 63893 |
| rs538474665 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | UBE2O | GRCh38.p7 | 17:76415799 | ACAGAGCAAGACTGT[A/G]TGTGTGTGTGTGTGT | 63893 |
| rs538494150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454597 | AAGCAGATGGATCAC[C/T]TGATCACCTGAGGTC | 63893 |
| rs538507824 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451742 | TCTTGAAGGGGAGGG[C/G]AAGTAGGAGAGAAAG | 63893 |
| rs538528864 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432475 | AACCTATTTAGCAAC[C/T]CCTTTCTCATCCTAG | 63893 |
| rs538536115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408814 | AAACCTTGGAATAAA[C/G]CCAATCCCTACTGTT | 63893 |
| rs538538585 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427049 | TTATGGCCTCTACTG[C/T]TGCTACTTGGCATTT | 63893 |
| rs538538632 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401732 | AATACAAAAATTAGA[C/T]GGGTGTGGTGGCACA | 63893 |
| rs538570102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445879 | GAAGCAATTCCGAAC[G/T]GGCACTCTTGCTCAG | 63893 |
| rs538655753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433421 | CATGGCTTCCAGGAG[C/T]TGGGAGGGGTGCAGG | 63893 |
| rs538690476 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401771 | ATCCCAGCTACTCGG[A/G]AGGCTGAGGCCAAAG | 63893 |
| rs538727373 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76417390 | TTACAAAGAACAGAA[C/G]ACAATGCAAAATTTC | 63893 |
| rs538796747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407321 | GCTGGCGTGACGGTG[C/T]CACTTTTCTAAATCA | 63893 |
| rs538837844 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416925 | GCAGTGAGACAAAGC[A/T]GCGGCTGGTCACATG | 63893 |
| rs538868505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401295 | CCTAAAACAAGTCCT[A/G]TGGCTCCACATCAGC | 63893 |
| rs538906708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395334 | CTACAGGCGCCCGCA[C/T]GGTGGCGGGAGAGTT | 63893 |
| rs538938203 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452183 | AAAAGGAGGCAGCAG[A/G]GTAAAACAAAAAGAG | 63893 |
| rs538964856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76409257 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCTATTG | 63893 |
| rs538965258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438886 | ATAGGTGACGCCATG[C/T]ACACCGAGGGCACAG | 63893 |
| rs538973925 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390575 | ACATGTGCTCTCCTG[C/T]GGGTCTGCAGGGAAC | 63893 |
| rs538990251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418832 | CGTCGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 63893 |
| rs538990561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425052 | ACTTTTTTGTATTTT[C/T]AGTAGAGACGGGATT | 63893 |
| rs539040407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413952 | CCTAAGCCCGAGTTT[C/T]CAGTTTGGACTGGAT | 63893 |
| rs539053296 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76453056 | GGGACGGGGGCTGCG[C/G]CTGGGGCCGGGACTG | 63893 |
| rs539079928 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76410478 | CCAACGCACCCGCAG[C/T]GCCACAGCTGAGAAG | 63893 |
| rs539149607 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439323 | CCAGCACTCTCTCAC[C/T]TGACTTCTTCCACCC | 63893 |
| rs539210499 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76450703 | CTCAGCTCACCGCAA[A/C]CTCCGCCTCCCTGGT | 63893 |
| rs539225220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407825 | TCCCGTGGGGTCTCC[A/G]GACAACAGCAGCTCC | 63893 |
| rs539307099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76399248 | AAGGCCACCACCATC[C/T]CACCCTCTGCACCAC | 63893 |
| rs539395032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416142 | ATGTGCGTGTATAGA[C/T]ATATAAAGTGTGGCT | 63893 |
| rs539450501 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397736 | TCTGGCTACACGCCT[A/G]TGGCCCCCGGCCCAA | 63893 |
| rs539471755 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453570 | TGCAGAAAGAGAAAG[A/G]TACTGTCCCTGTCCT | 63893 |
| rs539542037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447606 | TCCTGGAGGACGGCC[A/G]GGGTTACTTTAAATG | 63893 |
| rs539557582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440551 | CAGGCTGGTCTCGAA[C/T]TCCTGGCCTCAAGTG | 63893 |
| rs539562482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405085 | TGGCTGCTGTGCTCC[A/G]CCTTCTGACCCAGGA | 63893 |
| rs539770702 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447392 | TGTTGTGAGCGTGAA[A/G]TAAAACATCTAAAGC | 63893 |
| rs539825362 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE2O | GRCh38.p7 | 17:76437143 | AACAAAGTGAGACTC[A/C]ATCTTTAAAAAAAAA | 63893 |
| rs539994520 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405765 | AGGCAGAGCGCGTCA[C/G/T]GCCCACAGGCCTCCT | 63893 |
| rs540024258 | snp | A/C | 1.65116e-05 | 0.00287324 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391811 | TGTCCACCTCTCTGT[A/C]CCCTGAAACACACAG | 63893 |
| rs540190281 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76449754 | AGAAACCCCGTCTCC[A/C]CTAAAAATACAAAAA | 63893 |
| rs540206902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429946 | ATTGAGTATTTTCTG[C/G]TTTGCAGAATTCAAA | 63893 |
| rs540251396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393846 | AGTGATGAGCTGAGA[A/G]GCAGGGAAGGCAGAG | 63893 |
| rs540272961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423641 | GAGCTTGCAGTGAGC[C/T]GAGATCACAACACTG | 63893 |
| rs540387286 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429473 | CTTCAGCCTGGGAGG[A/C]AGAGGTTGCAGTGAG | 63893 |
| rs540402196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454746 | GAGAATTGCTTGAAT[C/T]TGGGAGGCAGAAGTT | 63893 |
| rs540403702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418406 | CCAGCAACTGCGAGG[A/C]GCCATTTGGCTGTCT | 63893 |
| rs540465898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448348 | ACATTACATCACTAA[A/G]AACAATTGCTTTTAA | 63893 |
| rs540466077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418869 | CCACCGCGCCTGTCC[A/G]GAACAGATTTTAAGG | 63893 |
| rs540485027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442279 | ATTAGGATGCCCATA[C/T]GTCCCAGTCCTGGAG | 63893 |
| rs540489786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449111 | TCATGAAGGCAGCAG[A/G]GAAAGGACATGACTT | 63893 |
| rs540490382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405745 | CGACCAGCACCCAGA[C/T]CCACAGGCAGAGCGC | 63893 |
| rs540518155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406486 | TGACCTGGGGGCACT[C/G]AGAGGTCACCACCAA | 63893 |
| rs540544367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436492 | CTTCGGTGCTGGATT[A/G]TCAGAGACTGAAGAA | 63893 |
| rs540563772 | snp | C/G | 6.78104e-05 | 0.00582242 | intron-variant | UBE2O | GRCh38.p7 | 17:76399434 | CATTGGGGAGGGGCA[C/G]AACTCTGAGTTTACC | 63893 |
| rs540662049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415355 | TTCCACAGGAGACTG[C/G]GTGGCTTGGAGAAGT | 63893 |
| rs540689276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453929 | CAATTTTTGGCACTG[C/T]CACTTACTAATCTAT | 63893 |
| rs540708724 | in-del | -/A | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453938 | GCACTGCCACTTACT[-/A]ATCTATAAAAATAGG | 63893 |
| rs540717328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411692 | AATACCAGATTTTTT[C/T]TTTTTTTTCTTGAGA | 63893 |
| rs540727156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76451107 | CTCCCTGAGTCCTAG[C/G]GCAGGAGGCCACAAC | 63893 |
| rs540786892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445232 | GCCTTTTTTTTTTTC[G/T]TTTTCCAAGCATGAC | 63893 |
| rs540787317 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76408849 | GGTGCCCTGCTTGTA[G/T]TTTAAAAAAAAATTG | 63893 |
| rs540869148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439538 | TGATGGCCAATAGAA[C/T]GTATGCCCAGGCATT | 63893 |
| rs540948527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433802 | CAAGGTAGGAGGATC[A/G]CTTGAGGAAAGGAGT | 63893 |
| rs540959175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393419 | TTTTGTATTTTAATA[C/G]AGACGGGGTTTCACC | 63893 |
| rs541025241 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76406530 | AGTCGCCGAAAAAGG[A/G]AGATACTGGCTCAAG | 63893 |
| rs541055273 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE2O | GRCh38.p7 | 17:76406275 | CAAAAGCCCAGGCAC[A/G]TGATGCTCCCACCAG | 63893 |
| rs541070771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76400878 | TTTATCCCCAAAGCC[C/T]TTTGAGATCAACAGG | 63893 |
| rs541110423 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444072 | CTAAAAAGACAAATA[C/T]TACTCGGACGTGGTG | 63893 |
| rs541139721 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451933 | AGCATCACCCCAAAA[A/T]CCATACGGGAGTCAG | 63893 |
| rs541139767 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418110 | CCCTGGGGTCTGGGA[C/T]AGCTGCCCCACACTG | 63893 |
| rs541141358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420754 | AGTGCAAGCTGGGGT[C/T]TTGCACCACCAGGTG | 63893 |
| rs541156915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395470 | GTGCTGGGATTACGG[C/G]TGTGAGCCACTGCGC | 63893 |
| rs541175289 | snp | C/T | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451573 | ACAGACCCCGCTTTG[C/T]AGTTTGACATGAAAC | 63893 |
| rs541242987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76402904 | AGCTGCTCTTCCCAG[C/T]GAGGAGGAAGTGGTG | 63893 |
| rs541245815 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389149 | AACCTGGAAGGAGCT[C/G]AACTGGTCAGTTGTA | 63893 |
| rs541308374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76396920 | CCGCACAGCTGATGG[C/T]GACTGGGCTCATGAG | 63893 |
| rs541345579 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435974 | TCGTTAGGCCCCGTG[C/T]GGTGGCTCACGCCTG | 63893 |
| rs541367065 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390704 | ATGGAAAATCGGCAA[C/T]AGGGTTCCGATTTTC | 63893 |
| rs541374332 | in-del | -/AAAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415903 | CATACACGTATATAC[-/AAAT]ATATACACATGCACA | 63893 |
| rs541472507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76444534 | AGAGCATAAGGCTGA[C/T]GGATCAAAATGAGGA | 63893 |
| rs541497573 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76441767 | CCATTTATTCATGCT[C/G]TCTTCACTTCCCCCT | 63893 |
| rs541503822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441946 | CGTTCCTGATTCATT[C/T]GCAGTCGGGTGGGGC | 63893 |
| rs541507146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401346 | GCAGAGGTCATCTGG[C/T]GCCCTTGTTCAAACA | 63893 |
| rs541514802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76392380 | GCAATAATGGCTCAC[G/T]GCAGCCTCCCAAGTA | 63893 |
| rs541557159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438530 | TATTCCTCAAACGTC[C/G]TTCACACCTTTGCGC | 63893 |
| rs541567607 | snp | A/G | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389188 | GAGACTACAGCTGCT[A/G]GGAGGCTGCTCTAAG | 63893 |
| rs541622523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76432248 | GTCTTAGACCCGTCA[A/G]ACTGCTACGGAAAGG | 63893 |
| rs541731169 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438384 | AAAAACTTAAAGGCT[C/T]CTCGTCGCTCTTCTG | 63893 |
| rs541769973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76404474 | AGAAAGGCTGGGAAG[C/T]GATTCCAGATTGGAG | 63893 |
| rs541802678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76423053 | TCCCAATGGGTGGCG[C/T]GGGCAGAATCCCCAA | 63893 |
| rs541905853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421265 | TGCTGTCAGCGCTCA[C/T]GGCTGACACCACATG | 63893 |
| rs542014655 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452521 | GGCCCGCCCGGTCCC[A/G]GGCCAGCAGTGCCTG | 63893 |
| rs542076053 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | AANAT, UBE2O | GRCh38.p7 | 17:76453145 | GGGATCCGCCATAAC[C/T]GCTCTGCGCGAGTCT | 63893 |
| rs542179740 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76424172 | CTCGGCCTCCCAAAG[G/T]GCTGGGATTACAGGC | 63893 |
| rs542183879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76431150 | AAAAAAGAGGCAACC[A/G]GAGGTTTTTAATCTT | 63893 |
| rs542215423 | in-del | -/C | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452095 | AGCTGTCAGAATCCT[-/C]CCCCCCCAAGTACTA | 63893 |
| rs542255272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76427894 | TTCAACTCCATGCTT[C/T]ACGTGTTCATGCAAA | 63893 |
| rs542347862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419019 | ACTGCCACGGTGACT[C/T]GCGCTGTAATACCAG | 63893 |
| rs542402155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76449845 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 63893 |
| rs542408916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414112 | TTTACCAGCAAAGCA[A/C]AAATGGCCAGGGGGC | 63893 |
| rs542473534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450309 | TGGTCAGTAACAGAC[C/G]AGGAGACATTCAGCT | 63893 |
| rs542479125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76409863 | CTCCTGCAGGGGGGA[C/T]GCAGACAGACAGACG | 63893 |
| rs542536689 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403632 | GTGACATATTTAGAT[A/G]TGTGTATACATATAA | 63893 |
| rs542563591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411747 | TTGGAGGGCAGTGGC[A/G]CAAGCAGGGTTCACT | 63893 |
| rs542647954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76412406 | CCCTCCCTGACCCCC[C/T]ATCTCTTATTGTCTG | 63893 |
| rs542711314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405950 | GCTTTGCGTTCAATC[C/T]TTTTTCTGCCCTCTG | 63893 |
| rs542768683 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411745 | GGTTGGAGGGCAGTG[A/G]CGCAAGCAGGGTTCA | 63893 |
| rs542792808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76436595 | GCCCCTGCCCTGCAC[A/G]CTGTCCCTCGCCTGC | 63893 |
| rs542919341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430568 | ATGAATCAGATCCTC[C/G]ATGCAGATGATGCCA | 63893 |
| rs542966486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76408303 | AGGTGCTTCCTACCT[A/G]GCAGACAGTTCTCCA | 63893 |
| rs543029900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408950 | CAACCTCAGAGTTGG[C/T]GAGCTATTTATTGTC | 63893 |
| rs543097096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448513 | ATCAGGGATGTTTCA[C/T]ACACACAGCTTCATA | 63893 |
| rs543124364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76442464 | GAATACTATTTGTAG[C/T]AAGTGGGAGGGAGCA | 63893 |
| rs543129266 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433043 | CTCAAAATGCTAAAC[A/G]TAGATTTACCTACCA | 63893 |
| rs543152088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403715 | CCTAGCATCCAGATC[G/T]TGGGTTTTAAAAATA | 63893 |
| rs543165909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76439732 | TCTTGCCTTTATGCG[C/T]ACTGGACTTCCCGCC | 63893 |
| rs543188461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76396992 | TGGCTTTTGCAGTCC[C/G]TAGGTCTCTGGGAGA | 63893 |
| rs543207193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393442 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCGAA | 63893 |
| rs543286529 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419041 | TAATACCAGTACTTT[A/G]AGAGGCTGAGCTTTG | 63893 |
| rs543313655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76428017 | TTCCTGCTTTGCTTT[C/T]GGTTCTCTGTTTTTC | 63893 |
| rs543354715 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454225 | CTCACACCTGTCATC[C/T]CAGTACTTTGGGAGG | 63893 |
| rs543374722 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417605 | AGGACATGGATGGAG[A/G]CCAAATGAGAGTGCA | 63893 |
| rs543442723 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414604 | GCAATACAGTGCTGC[C/T]GCATCACCGCCTGGA | 63893 |
| rs543512684 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389266 | GCTCCAGGACAAGAA[C/G]TACAAAAGGCATGCA | 63893 |
| rs543537660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76417342 | GGGCAGGTCCCTAGA[C/T]GAGGACCTCTTCCCT | 63893 |
| rs543549596 | snp | C/T | | | missense | UBE2O | GRCh38.p7 | 17:76391340 | CTGGCCTTGGGCACC[C/T]CGTTGGGCAGTGCCT | 63893 |
| rs543557202 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404357 | CAGGGCAGAGCTCTG[C/T]GGCGGGCCTGCCAAG | 63893 |
| rs543581646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440310 | AGTAAAATATATTAA[A/C]ATTAATTTCATCTCT | 63893 |
| rs543626285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397448 | TCCTTTCTCTCCTTC[A/T]CTGTTAGAGCTTTCT | 63893 |
| rs543640596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434433 | CTGGAAATCACAGGG[C/T]ACATTTGTCTTCCTG | 63893 |
| rs543680120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420510 | ACCGAGCAACCCTAC[A/G]TGCAGGCCAGGAGAA | 63893 |
| rs543693344 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440916 | CCCCTTATCTAGAGG[A/G]CAGGGCCTGTGTGGG | 63893 |
| rs543746568 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76415490 | CTACACCTGGACCAA[C/T]TGGAACCATGCTGCC | 63893 |
| rs543840935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438931 | CTGCCCCATAAAATC[C/T]TCCTAACTGGCCTCC | 63893 |
| rs543922641 | snp | A/G | 0 | 0 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389734 | CTCTGCTGGCTGGGC[A/G]GTCACAGCACAGCAC | 63893 |
| rs543938742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433163 | CAGCATTATTCAGAA[C/T]AGCCAAAAGGTGAAA | 63893 |
| rs543956201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426238 | CGAACGGGGCTCAAG[C/T]GATCCTCCTGTCTTG | 63893 |
| rs543974144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429830 | GTGTGCAGACGTTCA[C/T]GAATCCCTCTTTCAG | 63893 |
| rs544000868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426024 | CTTACATGCCTAAAA[A/G]GAGGGTCTCACTCTG | 63893 |
| rs544065023 | in-del | -/ACAAAAAAAA | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76425224 | CTCAAGGTCCTTTCG[-/ACAAAAAAAA]AAAAAAAAAAAAAAA | 63893 |
| rs544089854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76429295 | GCCTGTGATCCCAGC[A/G]CTTTGTGAGGCTGAG | 63893 |
| rs544096896 | in-del | -/ACACACAT | 0.461813 | 0.132798 | intron-variant | UBE2O | GRCh38.p7 | 17:76435410 | TACAGATACACACAC[-/ACACACAT]ACACACACACACACA | 63893 |
| rs544112432 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443496 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCGAA | 63893 |
| rs544164134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428586 | CAGCTCTGATTCCTC[A/G]GAGATACATTTTTCT | 63893 |
| rs544168280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421621 | CCGCCCACCTTGGCC[C/T]CCCAAGGTGCTAGGA | 63893 |
| rs544218045 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76392988 | CTCAGCCAGACGTGA[C/T]GGCTCACACCTGTAA | 63893 |
| rs544231104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422200 | CTCCCAACTATTTCA[C/G]TCACTCCACTCATTC | 63893 |
| rs544325641 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453257 | CTGACGTGTCCCTGC[A/G]TGGCGCCGTCGTCAG | 63893 |
| rs544347250 | snp | A/C | | | upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453218 | GGCGGGACCAGCGGG[A/C]GCCGGGGGCGGGGCC | 63893 |
| rs544387375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423473 | CCGAGGTGGGAGGAT[A/C]ATGAGGTCAGAAGAT | 63893 |
| rs544401176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447260 | AACAAAGTACATTTA[G/T]TTCAATTTGTATTCA | 63893 |
| rs544441400 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399202 | CCACTTGGGAGAGCT[C/G]AGGCAAATGTGGTTC | 63893 |
| rs544460144 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454990 | AAATTAGCCGGGCGC[A/G]GTGGCAGCCGCCTGT | 63893 |
| rs544478300 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453725 | AATTCCAAGCAGTTC[A/G]AACGTCATGACCCCT | 63893 |
| rs544488832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76412478 | TGACAGTGGCCAACT[A/G]GGGGTGTGGGAGAGA | 63893 |
| rs544494337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411506 | TCCAAAAGCAGGGGC[C/T]TGCATGGAGCCTAAG | 63893 |
| rs544511708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418292 | CACACAAAAACTCAT[C/T]TTATCACAGTCCTGA | 63893 |
| rs544516701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441978 | TTCTTTTTCCAATAG[A/G]GAGCCTCGTTCGTAC | 63893 |
| rs544539679 | snp | C/T | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76441289 | TCAAAACAACTACCA[C/T]ATTTACATCCTAAAA | 63893 |
| rs544575688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419032 | CTCGCGCTGTAATAC[C/G]AGTACTTTGAGAGGC | 63893 |
| rs544634783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419830 | GTGACTAGAAGGGAG[A/C]GAGCTGGTGTGAAAG | 63893 |
| rs544640653 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76394615 | GTACTTATGGTGATA[C/T]ATGAAAATGTAAAAA | 63893 |
| rs544746395 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76410695 | GCTCCCCGAAGCTAT[G/T]CTGGGGGCCACTCAG | 63893 |
| rs544800598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76444667 | GAAAATGACTGAAGG[C/T]GAGAGCAGGTCATGA | 63893 |
| rs544803619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450399 | ACCCTCCAAAACAAA[C/T]CTATTCTAAATCCTA | 63893 |
| rs544803807 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442371 | ACACACCTAGTACGG[G/T]GGGTGGGAGACAGAG | 63893 |
| rs544863978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445113 | AAAAGACCAGCTCTC[C/T]TGCAGGATGCAAATG | 63893 |
| rs544898757 | snp | A/G | 3.56132e-05 | 0.00421963 | intron-variant | UBE2O | GRCh38.p7 | 17:76405157 | AGGTCGTGCCGCCGA[A/G]AGAACCAGAGGGCCC | 63893 |
| rs544924683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439000 | CGCCAAATCACCCAT[C/T]GTAAACTCTGATGTA | 63893 |
| rs545027572 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76413255 | CACCCCCATCCCACA[A/G]TGTTAATGCAGCTTG | 63893 |
| rs545090572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406378 | ATCATGGATGGGTCT[C/G]TGTGTGTGTCCACCT | 63893 |
| rs545132232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393963 | TGAGTGAGATGTGGG[A/G]AAAACAGAACAAAAC | 63893 |
| rs545142073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415116 | TCCTGTGGCTGCCGG[G/T]CATCCCTGAGAACAA | 63893 |
| rs545207211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408103 | GGGCACTGGCTTTCT[C/T]CAAATAAGCCCATAC | 63893 |
| rs545217948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394745 | AGGCCTATGATTCGG[C/G]GAGAAAGGGAAGTGA | 63893 |
| rs545257795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437761 | ATATATATCATGATA[C/T]GTAAGATGTGAACAT | 63893 |
| rs545304271 | snp | A/G | 1.68721e-05 | 0.00290444 | missense | UBE2O | GRCh38.p7 | 17:76402113 | TTGGCGCCATCTTCC[A/G]TGTTCATGGAGCACC | 63893 |
| rs545305768 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76424873 | TTTTTATTTTTTATT[A/T]TTTTTTTTTGAGACA | 63893 |
| rs545323978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76431341 | ACATGGTGAAATCCC[A/G]CCTCTACTAAAGATA | 63893 |
| rs545418917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448984 | ATAAGAGACACTGGC[C/T]ACTAGCTCCTTTTGA | 63893 |
| rs545437391 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76423892 | GCTACTTCCAGGTTG[C/G]GTTCTTTTTTTTTTT | 63893 |
| rs545480762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443172 | AACTGCTGACTCATA[A/G]TGGTTGGGGGTTAGC | 63893 |
| rs545505950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437410 | AGCCAAGATCATGCC[A/T]CTGCACTCCAGCCTG | 63893 |
| rs545507073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76412330 | GCACTGGAAACTTCT[A/G]AATTCCAACTTGATA | 63893 |
| rs545523264 | snp | A/G | 1.65677e-05 | 0.00287812 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391576 | GTCACTGTCGAAGCC[A/G]GCTTCGTTGTAGTAT | 63893 |
| rs545525187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76398156 | GCCCAGAGGACTTTC[A/G]GGTCTTGTCTCCTAG | 63893 |
| rs545540947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447057 | CTGGCACAACTTCCA[A/C]CTATCCCAACATCCT | 63893 |
| rs545542100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443767 | TGCAGCTACAAGCAG[A/G]GAGGTCACTCCAAAA | 63893 |
| rs545546249 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415497 | TGGACCAATTGGAAC[C/T]ATGCTGCCATTCAAG | 63893 |
| rs545561474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76404327 | CCAGCACTTTGGCTA[C/T]GGGGTACCATGAACC | 63893 |
| rs545600248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434466 | AACTGTAAAGGACAC[A/G]CCAATAGTCCTGCCA | 63893 |
| rs545685817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432187 | AAGGCCCCCTATCGC[A/C]AGGCACACACACCCG | 63893 |
| rs545698872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422287 | CAACACGGGGAGAGG[A/G]CATGGGCAAAGGGCG | 63893 |
| rs545732670 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389098 | GGAGTTGTGGCACCT[C/G]TCCACCGCCAGGTGC | 63893 |
| rs545758000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395171 | GTGAGCCACCGCACC[C/T]GGCCTATTTCAAAGT | 63893 |
| rs545780470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76439514 | TGATGTGTGATGACG[C/T]CACTGCTCTGATGGC | 63893 |
| rs545790415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429190 | CAGGCATGAGCCACC[A/G]CGTCCAGCCAGCCCT | 63893 |
| rs545802313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403769 | TTCTTGGAGAAATGG[C/T]TGATTCTGGGGCTGG | 63893 |
| rs545875767 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425480 | AGCTGTTTGAATATT[C/T]ACCTCCATACATATA | 63893 |
| rs545944106 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401943 | TAGACCCTCTGGCGC[A/G]CACCCGCCCCTTTTC | 63893 |
| rs545947555 | in-del | -/TGTATATGTA | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76416243 | ATGTGTATATATGTG[-/TGTATATGTA]TGTATATGTATATAT | 63893 |
| rs546163989 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415676 | TGGGTGTGGTGGTGC[A/G]CACCTGTAATCCCAG | 63893 |
| rs546173276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76409055 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG | 63893 |
| rs546262613 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422431 | CTTCCTCCCGTTCAT[C/T]ATATGCTGTAGACCA | 63893 |
| rs546289487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426745 | TTTTTTGTTGGGACT[C/T]TGGTTTTTAATCCTC | 63893 |
| rs546384922 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431470 | GCAGTGAGCCGAGAT[C/T]GCACTCCAGCCTGGG | 63893 |
| rs546390656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421218 | GAGCTGAGCCCAACC[A/G]TAGGGAAACACTGCA | 63893 |
| rs546409589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455011 | AGCCGCCTGTAATCC[C/T]AGCTACTCGGAAGGC | 63893 |
| rs546453934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415923 | TATACACATGCACAT[A/G]CACGTATATACGTAT | 63893 |
| rs546504326 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452416 | CCCCAGAACCTGAGT[A/C]CCCACGGGAGTCGGT | 63893 |
| rs546515384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76416036 | ACACACACGTATATA[C/T]GTGTGTGTACATATG | 63893 |
| rs546555056 | snp | C/T | 3.34767e-05 | 0.00409112 | missense | UBE2O | GRCh38.p7 | 17:76399863 | TGGTCCCGGGAACAC[C/T]GGGTGTCTGGGGAGC | 63893 |
| rs546706348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448190 | CACTGAGGCCCGAGG[A/G]CTAGAAGGGGAAAAA | 63893 |
| rs546709270 | in-del | -/AAGGGAGCAGGAAGGAGAAG/AG | 0.00676609 | 0.0577691 | intron-variant | UBE2O | GRCh38.p7 | 17:76403178 | GTGTTTACTAACAGA[-/AAGGGAGCAGGAAGGAGAAG/AG]AAGGGAGCAGGAAGG | 63893 |
| rs546721269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76441428 | GGCGGATGATGAGTC[C/T]GCCTCATCCCTTTCC | 63893 |
| rs546727920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411845 | CACATGCCACCACCC[A/G]GCTAATTTTATTTTT | 63893 |
| rs546750906 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430908 | CAGCTTTTCTTGCCA[C/T]CCTAGCCTTTCAAAT | 63893 |
| rs546847407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436038 | GATCACCTGAGCTCA[A/G]GAGTATGAGACTAGC | 63893 |
| rs546870800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442699 | GATAGAGCAGGATGT[A/G]TAGGTGAGGGGCCCT | 63893 |
| rs546905770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443307 | TATATTTTTTTCCTC[A/G]AGAAAGAGTCTCACT | 63893 |
| rs546932164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436827 | TGAAAGATCAACGAG[C/G]AGCATTTATTTCAAC | 63893 |
| rs546944587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410306 | CCAGTGGTTCTCACC[C/T]AGGGGTAATTTTGCT | 63893 |
| rs546986248 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76449651 | CGGGCGGGTGCGGTG[G/T]CTCCTGCCTGTAATC | 63893 |
| rs546986831 | in-del | -/C | 0.00239616 | 0.0345303 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390540 | GAATTGTTGGCGCAA[-/C]CCCACACTTCATGCA | 63893 |
| rs546998259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429464 | GGAGAAGTGCTTCAG[C/T]CTGGGAGGCAGAGGT | 63893 |
| rs547017238 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411855 | ACCCGGCTAATTTTA[-/T]TTTTTTTTGTAGAGA | 63893 |
| rs547019596 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76451156 | AAATGAGTTGCGTTC[C/G]AAAAATCACGAATCT | 63893 |
| rs547025227 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76407714 | AGCAGAAAAAAACAG[C/T]TGGTGAAAGCTGGCA | 63893 |
| rs547069686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444268 | AAGAGGGTGTGGTCA[C/G]CTAGGCACCGTGGCT | 63893 |
| rs547095247 | snp | G/T | 1.65272e-05 | 0.0028746 | missense | UBE2O | GRCh38.p7 | 17:76397824 | ATGATGGTCTTTGAG[G/T]TGTCAGCCCACACCA | 63893 |
| rs547157924 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416399 | ATGATTCTGATGCAC[A/T]CCCCCCAGAGAAACA | 63893 |
| rs547167660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432818 | AGATATACACATGGC[C/G]AATAAGCACATGAAA | 63893 |
| rs547183186 | snp | C/T | 0.000309443 | 0.0124349 | intron-variant | UBE2O | GRCh38.p7 | 17:76398611 | GAGAAAGGGAAGTGA[C/T]TAGCTAAGGGATCCC | 63893 |
| rs547196685 | snp | A/G | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390365 | GGCTATAACGTGGTC[A/G]ACAGGCCATGTATAG | 63893 |
| rs547219965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76392575 | GCCTGGCCCTTGCCT[A/G]GAATCATTGAACCCT | 63893 |
| rs547230982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433320 | CCTTGAAAACATCAC[A/G]TTAAATAAATCAGTC | 63893 |
| rs547296096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422547 | GGAACACGAGACAGT[C/T]CTGCAGGTGTCCGAG | 63893 |
| rs547306982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393028 | TTTTGGGAGGCCAAG[G/T]TGGGAGGACTGCTTG | 63893 |
| rs547316922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425703 | ACCAAGTGGTGTTCC[A/G]TGTCCTCACACAACT | 63893 |
| rs547350653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393622 | GTAGTACAAGCAGTT[G/T]CAAGCTGAAAGGCAG | 63893 |
| rs547365098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450596 | CTGCAAAATCTATCC[A/G]AAGTGGTGCCTCAAA | 63893 |
| rs547406751 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | UBE2O | GRCh38.p7 | 17:76395552 | GCCTGGACACACGGC[A/T]GAGTCAGCCCTCACC | 63893 |
| rs547424605 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76444753 | CACACTGGGGGACCA[C/G]AGAAATGCTTTCTTC | 63893 |
| rs547446335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401660 | GTGGGCAGATCACCC[A/G]AGGTCAAGAGTTCGA | 63893 |
| rs547490181 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76395155 | TGCTGGGATTACAGT[A/C]GTGAGCCACCGCACC | 63893 |
| rs547495298 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428807 | TGCACATATTGTGTA[C/G]CCATGTCAATTCCCT | 63893 |
| rs547534219 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76430696 | CTGATTTCAGATTTG[G/T]GTTCCCCTTGTAATA | 63893 |
| rs547569920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418782 | CACCGTGTTGGCCAG[G/T]ATGGTCTTGATCTCC | 63893 |
| rs547581930 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446673 | CAGCCGAAGGATGAC[A/G]GCAGCAGAGCGGACA | 63893 |
| rs547597651 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE2O | GRCh38.p7 | 17:76424311 | TCTCCCAGGTTCAAG[C/T]GATTCTCCTGTCTCA | 63893 |
| rs547614944 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389446 | GGACACAAAGGCAAC[A/G]GAGCCCAGATGAATG | 63893 |
| rs547633252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413769 | CAAAAAACATGCAAA[C/T]CAACACAAAACCCAA | 63893 |
| rs547697697 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76414535 | CCAGGGACAGCCCCC[A/C]CGCCCTCACCCCTGA | 63893 |
| rs547702952 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390021 | CGTCCCCTTCGGATT[G/T]AGCCTGCAGTTTGTA | 63893 |
| rs547748940 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76430196 | TGGAGATCTTTTGTT[A/G]TTGTTTTCTCTCCCA | 63893 |
| rs547782476 | snp | G/T | 0.000102244 | 0.00714924 | intron-variant | UBE2O | GRCh38.p7 | 17:76391648 | TCCCTCAGTGGGTGA[G/T]AGAGGCCCACAATGC | 63893 |
| rs547808245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76437459 | CATCTCAAAAAAAAA[A/G]AAAAAGAAAAAGAAA | 63893 |
| rs547840926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397643 | AACTGCAGGCCTGCA[C/T]CAAGGGCTGTGTGGA | 63893 |
| rs548015366 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433669 | TGGAGTGAGTATTGC[A/G]CCACTGCATTCCAGC | 63893 |
| rs548018136 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76435837 | CAAAGCTCAGTGACA[-/C]CCCGGCACAGAGGGG | 63893 |
| rs548045128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76422341 | CAGGCTGAGCTCAAG[C/T]CCCATCTCTCCTCCA | 63893 |
| rs548053729 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409482 | GCTCACTGCAACCTC[C/T]GCCTCTGGGGTTCAA | 63893 |
| rs548068347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410901 | CTCTCATTCATAACA[C/T]TGACCTTGACTGACC | 63893 |
| rs548112473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416427 | ACAGCTAAAAGGGAC[C/T]GCATCCCTCTGAGCT | 63893 |
| rs548132935 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422470 | GTTGTTCCCTCGCCC[A/G]TTCAGCAAACTGAAT | 63893 |
| rs548172847 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397447 | CTCCTTTCTCTCCTT[C/T]TCTGTTAGAGCTTTC | 63893 |
| rs548184355 | in-del | -/TATGTG | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76416191 | GTGTGTGTATATGTA[-/TATGTG]TATATGTGTGTGTAT | 63893 |
| rs548189059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434553 | CAAGCATGAATTAGG[A/G]TGACTCCTCGTCCTG | 63893 |
| rs548249797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428185 | AATCCAATCCATCTT[A/C]ATTCCCAGTCTTTTG | 63893 |
| rs548251129 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445191 | CTAGCTGGGAATATT[A/C]ATGTCATTGTTGGGT | 63893 |
| rs548269025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421789 | CCTTTCTTTCATGGA[A/G]TAAATGCCACGTGCT | 63893 |
| rs548323110 | in-del | -/AAAT | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76423383 | GACCCTATCTCTAAA[-/AAAT]AAATAAATACAGTAA | 63893 |
| rs548328841 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76416119 | TATGTGTATACATAT[A/G]TACATATATGTGCGT | 63893 |
| rs548365212 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450736 | AAGCAATTCTCCCGC[C/G]TCAGCCTCCCGAGTA | 63893 |
| rs548415910 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452849 | TCGGAGCACCCCGAG[A/C]TCCCGCGGCCCTCCT | 63893 |
| rs548421049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445711 | AAATAACTTGGAGTA[A/G]ATAAATCCAGAGAGT | 63893 |
| rs548444104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76402588 | CCGATGGCTCTCTGG[C/T]GGTGAGACTCTACCT | 63893 |
| rs548445270 | in-del | -/AAGAC | 0.00676609 | 0.0577691 | intron-variant | UBE2O | GRCh38.p7 | 17:76414307 | GTTTTCTATAGACTT[-/AAGAC]AAGACAAGAATACAA | 63893 |
| rs548476892 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453448 | TGGAGTGGCCACCGA[C/G]GAAGAGGGGAGTGGT | 63893 |
| rs548485347 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400078 | AGCACAGACTGTCCT[C/T]CTTGGCCATGGAAAT | 63893 |
| rs548528703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76420689 | GAAGCAGGAGCTTGA[C/T]AAAGGCATGGGAAGC | 63893 |
| rs548581786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429991 | AGTTTCATCCCTCCC[C/T]ATACAGACTGTCAAC | 63893 |
| rs548616958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440413 | GCCCATTGCCACCTC[A/G]ACCGCCAGGACTCAA | 63893 |
| rs548629901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415600 | ACTTGAGGTCAGGAG[C/T]TGCAGACCAGCCTGG | 63893 |
| rs548630700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448729 | CTGCTCCCTTACCTC[A/G]CAGGGGGCTGTTCTG | 63893 |
| rs548646634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433925 | CAGGCCCAGCTACAG[G/T]GTTTCCTGTAAATCC | 63893 |
| rs548677771 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76436379 | CACCTTTCCTATGTC[A/C]TTGCACTTTTGTATT | 63893 |
| rs548689502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408753 | AGGTGAACACTAGAG[A/G]GCACTGTGCCCACTC | 63893 |
| rs548818026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439908 | CTCGCTCCCTTATGT[A/G]CATCAGTCATTCACC | 63893 |
| rs548818777 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410233 | GGTGATATCCAAAAC[A/G]TTACCTGATTTTTGG | 63893 |
| rs548893948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443335 | ACTCTGTCGCCCAGG[C/T]TGGAGTGCCGGGGCA | 63893 |
| rs548917515 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76404980 | ATAACCACACTGGCA[A/G/T]CCTATGCTGGGGTTG | 63893 |
| rs549004513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394439 | ACGAACAGAGGAGTG[A/G]GAAAATGGAATGTGG | 63893 |
| rs549079272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436118 | CAGGCATGGTGGTGT[A/G]CACCTGTAATCCCAG | 63893 |
| rs549089114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406211 | GAGCACCTGATTGTC[C/T]CTTTACGCACAGCTG | 63893 |
| rs549159194 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403968 | ATTAATTATAACCAA[C/T]GAATAAAACAGAAAT | 63893 |
| rs549161358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442015 | ATCCTCCTAAGGTGA[G/T]GACTGGGTGCTGATA | 63893 |
| rs549208087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430043 | TAGGCCCAAACCTTA[G/T]TCCCACCTTGAGTGC | 63893 |
| rs549208583 | snp | A/C/G/T | 0.000101883 | 0.00713673 | intron-variant | UBE2O | GRCh38.p7 | 17:76399034 | ATGCAAACCCCACCC[A/C/G/T]CTCCGCGGAAAGGGC | 63893 |
| rs549247080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76393085 | GCAACATAGTGGGAC[C/T]CTATCTCTACAAAAA | 63893 |
| rs549272390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437937 | AGGCTAAATACACGC[C/T]TCGAAGGGAGGTGTC | 63893 |
| rs549296756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76394992 | GTGATTCTCCTGCCT[C/T]AGTCTCCCGAGTAGC | 63893 |
| rs549313532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430807 | AAGAAGCTGCAACAT[A/C]TTTTGGCCCTTTGGG | 63893 |
| rs549338532 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76401869 | CGACAGTGAGACTCT[A/G]TCTCAAAAAAAAAAA | 63893 |
| rs549349817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441558 | TACTAAAACTGAACC[C/T]ATTGACATCAACGAG | 63893 |
| rs549370292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76398653 | CCACATCTCAAGCCA[A/G]TGCAGAGTGCAGAAC | 63893 |
| rs549412786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423804 | TTGATAGAGGTGGCC[A/T]ACGGCACAGTGTCCG | 63893 |
| rs549418007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432914 | CACTAGGATGGCTAT[A/G]AACAAAGTGACAGTC | 63893 |
| rs549419087 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE2O | GRCh38.p7 | 17:76410697 | TCCCCGAAGCTATGC[C/T]GGGGGCCACTCAGAG | 63893 |
| rs549456312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76392723 | TTTGGGAGGCCGAGA[C/T]GGGTGGATCACTTAA | 63893 |
| rs549510326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438874 | CGCCATGCATGCATA[A/G]GTGACGCCATGCACA | 63893 |
| rs549605924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420750 | ATCGAGTGCAAGCTG[C/G]GGTCTTGCACCACCA | 63893 |
| rs549608755 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389577 | ACTTTATACAGATAT[C/T]GTAAGCAGTAGGCAT | 63893 |
| rs549627040 | snp | C/T | 3.79802e-05 | 0.0043576 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390894 | GGGGGAGTGAGCAGG[C/T]GGCGGCTGGCCTCTC | 63893 |
| rs549630873 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392949 | GTGCGACGCTATCTC[-/A]AAAAAAAAAAAAAGA | 63893 |
| rs549634787 | in-del | -/A | 0.0562307 | 0.157967 | intron-variant | UBE2O | GRCh38.p7 | 17:76437450 | GCGAGATTCCATCTC[-/A]AAAAAAAAAAAAAAG | 63893 |
| rs549668384 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76398181 | TCCTAGAGCCACCTG[A/G]TGGCAGCATCAGGGA | 63893 |
| rs549672194 | snp | A/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451420 | GAAGCAGGGTCCTGT[A/G]TGTGGATTTGTGTCT | 63893 |
| rs549699742 | snp | A/G | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390428 | AGGGATAGTGTTGAC[A/G]CTGGAGGACTAGGGA | 63893 |
| rs549708985 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426785 | GTGACGATCACTTTC[A/G]GAAGCGAATGCTTAT | 63893 |
| rs549799555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76439233 | GGGGTTCTCCAGTGA[C/T]TGTGCCTAGAACGCG | 63893 |
| rs549811385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76415761 | GTGAGCTGAGATCAC[A/G]CCACTGCACTCCAGC | 63893 |
| rs549862897 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76433372 | CTTCCATTTATATGA[A/C]ATGTCCAAAATAGGC | 63893 |
| rs550047322 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415969 | CATACACGTATATAC[A/G]TATGCGTATACATAT | 63893 |
| rs550073103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414548 | CCACGCCCTCACCCC[G/T]GACACCCTCTCTGAT | 63893 |
| rs550115747 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444695 | TGAGGAAATGGAGGC[A/G]GACATCCATTTCCCC | 63893 |
| rs550137122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76425020 | GGACTACAGGCACCC[A/G]CCACCACGCCCAGCT | 63893 |
| rs550175306 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76431508 | GTGCTCTGTCTCAAA[A/G]AAAAAGTCAACAAAA | 63893 |
| rs550179156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76424575 | ACTGAGTTAAATAAA[A/C]CATTAAAATTAATTT | 63893 |
| rs550316855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76420021 | ATGACATAACCTTGG[A/G]GCAGCAGAAAGCTGC | 63893 |
| rs550343367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76412683 | TCAAGACAGGGGTCA[C/T]GTGTGTTAGTGCATA | 63893 |
| rs550379956 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76414913 | CAGCCCAGGCCTGGC[G/T]CCTGCATTTGAAGGG | 63893 |
| rs550397726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450121 | TACATTATTTTGTCA[A/G]TAATTGGGTTCTCAA | 63893 |
| rs550398410 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413084 | GTGGAAGCAGGAAAC[C/G]TTGCTGAGGCCTAGG | 63893 |
| rs550448207 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76402786 | TGCCCCACCGAAGAC[A/T]GGATGGGGGAGGATC | 63893 |
| rs550454234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76405431 | GCCAGTTCTCCCACA[C/T]GCAGAGTGCGAGGTG | 63893 |
| rs550458585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450679 | CAGGTTGGAGTGCAA[C/T]GGTGCCATCTCAGCT | 63893 |
| rs550469603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76417191 | TTCCACCTGCCTGGC[A/G]CCTCTCCCTGACTCA | 63893 |
| rs550504483 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454205 | AAGTAGGCCGGGCGC[G/T]GCAGCTCACACCTGT | 63893 |
| rs550531586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444788 | GCTTGAAGATGATGT[C/T]ATCAACCTTCAGGGC | 63893 |
| rs550563103 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452159 | CTCACAAAGTTCCCT[A/G]CAGCAATTAAAAGGA | 63893 |
| rs550580364 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76428940 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 63893 |
| rs550624420 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452583 | ACTTTGCATGGAGTG[C/T]ACCCTCCACTGGGGC | 63893 |
| rs550636852 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422779 | TTTTCTTCACAGCAC[C/T]TACTGTTCCCACACC | 63893 |
| rs550642307 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76422425 | TGGCCTCTTCCTCCC[A/G]TTCATCATATGCTGT | 63893 |
| rs550650448 | in-del | -/AAAAAACA | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454829 | TCTGTCTCAAAAAAC[-/AAAAAACA]AAAAAACAAAAAAAA | 63893 |
| rs550654291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416483 | AGCGGTGTTCCCCTG[C/T]AGCTATGCTCCCCAG | 63893 |
| rs550690542 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453523 | ATGAGCTCCCTTGGC[A/G]TCCTAGCCTAGCCCC | 63893 |
| rs550699508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423050 | CAGTCCCAATGGGTG[A/G]CGTGGGCAGAATCCC | 63893 |
| rs550718952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411098 | GGCTGGAGTGCAATC[A/G]TGGCTCCATCTTCCA | 63893 |
| rs550737725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76418274 | GGAGGGCTCTCCAGG[C/T]CTCACACAAAAACTC | 63893 |
| rs550787449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410115 | AGAAGGCAGAAGGCA[C/T]GGTGCTGTTATTCAG | 63893 |
| rs550832531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440034 | GGATATAGCAGTGAC[A/G]GAGATGCTTCTGTGC | 63893 |
| rs550866215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448068 | AGGTGACAGCCAGGA[A/G]GAGCACCCAAGGGTT | 63893 |
| rs550917804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415954 | GCGTATACATATGCA[C/T]ATACACGTATATACG | 63893 |
| rs550963697 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | UBE2O | GRCh38.p7 | 17:76395348 | ATGGTGGCGGGAGAG[-/T]TTTTTGTAATTTTTT | 63893 |
| rs550970101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449357 | AGGCCGGTGAATCAC[G/T]TGAGGCCAGAAGTTC | 63893 |
| rs550983249 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76409224 | CTGCCAGCCTCGGCC[C/T]CCCAAAGTGCTGGGA | 63893 |
| rs551014207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76435559 | ACACAGGGAAACAGA[A/C]GCAGAGCTAAATTAT | 63893 |
| rs551024379 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76392430 | CCACCGTGCCCAGAT[G/T]ATTTTTTTATTTTGT | 63893 |
| rs551086906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403510 | CTCTTGAGCTCAAGT[A/G]ATCCATCTGCCTCAG | 63893 |
| rs551094615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444090 | CTCGGACGTGGTGGC[A/G]GGAGCCTGTAATCCC | 63893 |
| rs551154624 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76440481 | TACAGGCGTAAGCTG[A/C]CACGCTAAGATGATT | 63893 |
| rs551159932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438080 | ATGCTCATGAGAAGC[C/T]TGAGTCTCTGCCACG | 63893 |
| rs551305424 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76430281 | AGCAGAGTTTCTAGG[G/T]GAAGTAGATTTAAAT | 63893 |
| rs551318407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428224 | CCGTTTTTGCTCTTC[A/G]GAAGCTTTATGCCCA | 63893 |
| rs551398859 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76436959 | CAACATGTTGAAACC[A/G]TTTCTACTAAAAATG | 63893 |
| rs551427927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449968 | AAAACCATCACTACT[A/G]TAGTCCCAGCTACCT | 63893 |
| rs551481625 | snp | C/T | 2.41882e-05 | 0.00347757 | intron-variant | UBE2O | GRCh38.p7 | 17:76400575 | GCAGGTGGGACACGC[C/T]AGTCAGGGCAGGCTC | 63893 |
| rs551543582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76423819 | TACGGCACAGTGTCC[A/G]CAAAGGAACCAGAAC | 63893 |
| rs551547119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436760 | ACCCTCCTTCTGAAC[A/C]AAATTCAAAAAAGGT | 63893 |
| rs551570946 | snp | C/T | 1.66463e-05 | 0.00288494 | missense | UBE2O | GRCh38.p7 | 17:76401079 | CTGACAGCCACTGGA[C/T]GCTGGAGAAGATCTT | 63893 |
| rs551579254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393529 | TGAGCCACCACGCCC[A/G]GCCAACCCTGTCTTT | 63893 |
| rs551606311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430065 | CTTGAGTGCCACCAA[C/T]TGCCTCCAATTCCTG | 63893 |
| rs551609455 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE2O | GRCh38.p7 | 17:76395127 | GTGATCCACCTGCCT[C/T]GGCTTCCCGAAGTGC | 63893 |
| rs551667267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418638 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAGCT | 63893 |
| rs551677987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432419 | CATGCCACGGTACAT[A/G]TGACTGGTAAATATT | 63893 |
| rs551688169 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389421 | CTTCCCCAGGAAGGG[C/T]GTGTGTGAGGGACAC | 63893 |
| rs551718539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425061 | TATTTTTAGTAGAGA[C/T]GGGATTTGACCATGT | 63893 |
| rs551723203 | snp | C/T | 0.000198003 | 0.00994799 | missense | UBE2O | GRCh38.p7 | 17:76396481 | AGGCTCTCCAGGATC[C/T]TGATGGCCTCTTTCA | 63893 |
| rs551752149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76436152 | CTCAGGAGGCTGAGG[C/T]AGGAGAATTGCTTGA | 63893 |
| rs551867812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407316 | GGCATGCTGGCGTGA[C/T]GGTGCCACTTTTCTA | 63893 |
| rs551879163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433449 | AGGGAAATATGGTAT[A/G]ACTCCTAATGGGTAT | 63893 |
| rs551891330 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390364 | GGGCTATAACGTGGT[C/T]GACAGGCCATGTATA | 63893 |
| rs552030588 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455089 | CCTAGATCGCGCCGC[C/T]GCACTCCAGCCTGGG | 63893 |
| rs552068839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428096 | TGGGAGCGGTTCTAA[C/T]TTTAGCTCAAGCTAC | 63893 |
| rs552197513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439887 | TCCTGCAGGTGGAAC[C/T]AGGCTCTCGCTCCCT | 63893 |
| rs552399943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415002 | AAGGCAGAAAAGTGA[A/T]CAGCATGATTCCATG | 63893 |
| rs552432998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450731 | GGTTCAAGCAATTCT[C/T]CCGCCTCAGCCTCCC | 63893 |
| rs552466043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407826 | CCCGTGGGGTCTCCA[A/G]ACAACAGCAGCTCCA | 63893 |
| rs552487700 | snp | C/G | 0.0123036 | 0.0774623 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452676 | CCCTGGCCTCGGCCC[C/G]GCCGCCGACCCCCTG | 63893 |
| rs552502199 | snp | A/G | 0.00282087 | 0.0374497 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76453048 | CCGGCGCCGGGACGG[A/G]GGCTGCGGCTGGGGC | 63893 |
| rs552530440 | snp | A/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76425625 | CTCCATCCTTTCAAC[A/G]GTTCCACTGCATTAA | 63893 |
| rs552648226 | snp | A/C/T | 0.00597534 | 0.0543715 | intron-variant | UBE2O | GRCh38.p7 | 17:76420086 | CTCACCCCTACCCAG[A/C/T]GCAGCAGTGGCCCCC | 63893 |
| rs552702671 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453587 | ACTGTCCCTGTCCTC[C/T]AGGTGTTTCCAGTCT | 63893 |
| rs552711358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420620 | ACAACTCTGTAACTA[C/T]ATCTTTGCGAGACAA | 63893 |
| rs552760026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76447623 | GGTTACTTTAAATGT[A/G]CATTACTGAATTTCT | 63893 |
| rs552772803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415567 | CCCAGCACTTTGAGA[A/G]GGCAAGGCGGTTGGA | 63893 |
| rs552804733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405097 | TCCGCCTTCTGACCC[A/T]GGAAGGCTGTGCTTG | 63893 |
| rs552826233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393288 | TGTGTTTTTTTGAGA[C/T]GGAGTATAGCTCTGT | 63893 |
| rs552874916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445663 | ACATTAAATCCTCAA[A/T]CACAGAGTATAGCTA | 63893 |
| rs552920172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410505 | GAAGCCCTGAAGGTG[C/G]TCTGGAGACGCAGGT | 63893 |
| rs552936771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447081 | ACATCCTGTGCCTCT[C/T]TCCTTCCTCACTTGT | 63893 |
| rs552938236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439280 | CTTTGTTGTTATCGT[C/T]ATTTACAGTCCTGTG | 63893 |
| rs552981835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76404333 | CTTTGGCTATGGGGT[A/G]CCATGAACCAGGGCA | 63893 |
| rs552989235 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76416615 | ACACCAACCTCCCCG[C/T]GCTTCTCAAACACCT | 63893 |
| rs553002261 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428345 | CTCTGATACATTATG[A/G]TCCTTAATTTTCCCT | 63893 |
| rs553009309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76429791 | CAGGAGCAGGCAGGG[A/G]CATGGCTGGGATTTG | 63893 |
| rs553040922 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405154 | CAGAGGTCGTGCCGC[C/T]GAGAGAACCAGAGGG | 63893 |
| rs553084208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434933 | CAATAGAGGGGCTCG[A/G]GCGCGCCCATCCAGG | 63893 |
| rs553132496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441846 | GTTCCTGACTCCTTC[A/C]AAGTAATAGGCCTGG | 63893 |
| rs553148654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76439651 | TTATTGTGGTCCTCA[A/G]TAATTTTTAAGTTAA | 63893 |
| rs553171898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76399307 | TACCCCAGGCACCTA[A/C]GTTGTCTCGGGTGGG | 63893 |
| rs553191591 | snp | A/C | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455131 | GATTCCGTCTCAAAA[A/C]AAAGTAACTCTAGGC | 63893 |
| rs553197822 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76435893 | AGTCAGCTGGCCAGA[A/G]TTCTAGCCCTCTAGA | 63893 |
| rs553197871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442133 | GCTTCATTTCGACCA[C/T]AGGTGACACCAGCTC | 63893 |
| rs553260402 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395188 | CCTATTTCAAAGTAA[-/T]TTTTTTTTTTTGAGA | 63893 |
| rs553287301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428421 | TTCCTGGGAGCCTTC[C/G]TCAACTTCAAAGAAA | 63893 |
| rs553354745 | snp | A/G | 0.000119885 | 0.00774131 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396780 | GCCTTCTACCGAATC[A/G]TAGTCTGACTCCTCA | 63893 |
| rs553407455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76431065 | TGTGAAATTCCTTTG[C/T]TTTTTCCCAAGGGTT | 63893 |
| rs553444474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397378 | AGGGAAGGAGAGCCC[A/G]TGTAGCCCTTCTGCT | 63893 |
| rs553447852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76427681 | GGTCTGGTGCCAGCT[C/T]GGGCATTCCTGCAAC | 63893 |
| rs553468610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76431944 | TGACAGTCAGAACTG[A/C]TCCAGGCTTAGGGTG | 63893 |
| rs553581660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421551 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTCTCCAT | 63893 |
| rs553598627 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76424856 | ACCTGTTTCTTTTTT[A/T]TTTTTTATTTTTTAT | 63893 |
| rs553601037 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447401 | CGTGAAGTAAAACAT[C/T]TAAAGCACTAAGAGT | 63893 |
| rs553675941 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76453068 | GCGGCTGGGGCCGGG[A/T]CTGCCTCCGGGGCTG | 63893 |
| rs553736862 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76402779 | TCCTCTATGCCCCAC[C/T]GAAGACAGGATGGGG | 63893 |
| rs553754197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76393855 | CTGAGAAGCAGGGAA[A/G]GCAGAGCGCTAGCTG | 63893 |
| rs553790069 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76417690 | AGAGAGCACCACGAA[A/G]GGCCTTCGACTACAG | 63893 |
| rs553822872 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417711 | TCGACTACAGGAGGA[A/C]AGAATGCTAAGCATG | 63893 |
| rs553842169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394646 | TATTTTTTTAGTGTA[C/T]AAATAATGTAAAAGT | 63893 |
| rs553857141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423417 | TAAAAATGAGGGCCC[C/G]GCGTGGTGGCTCATG | 63893 |
| rs553912095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413069 | CTCAGTTTTGCGGGG[A/G]TGGAAGCAGGAAACC | 63893 |
| rs554073737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437232 | AAGGCAGGCGGATCA[C/T]GAGGTCAGGAGATCG | 63893 |
| rs554075244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448853 | AAATTTTATTCAAAG[A/G]ATGACTGGTGATGGG | 63893 |
| rs554107638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414674 | AGGCACAGCCTGCCC[A/G]AGGGACAGAGAAAGG | 63893 |
| rs554181429 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440660 | GCTGTGGCTCACATT[A/G]TATCTCTATTTTTCA | 63893 |
| rs554181598 | snp | G/T | 3.29935e-05 | 0.00406149 | missense, intron-variant | UBE2O | GRCh38.p7 | 17:76400196 | TTTTTTTCTGGACAT[G/T]CCCAGGCAATCTTGG | 63893 |
| rs554182229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415872 | ATATACATACATGTA[C/T]ATACAAATATATGTA | 63893 |
| rs554369346 | snp | A/G | 0.00319552 | 0.039844 | intron-variant | UBE2O | GRCh38.p7 | 17:76416003 | CATACACGTATATAC[A/G]TATGTGTATACATAT | 63893 |
| rs554411657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449618 | AATAGGTAGCAGCTT[A/C]TTAAAAAAAATAAGT | 63893 |
| rs554525824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421053 | TTTGGGCTGAGTTCC[C/T]GGTAAAAGGCATGGA | 63893 |
| rs554539899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440377 | TGCCTAGGCTTAAGG[A/G]CAATGGGTCGCACGA | 63893 |
| rs554571725 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418838 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 63893 |
| rs554667697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444544 | GCTGATGGATCAAAA[C/T]GAGGACAAGGACTGA | 63893 |
| rs554670103 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446139 | ATCCAGAAGCAGGCT[A/G]AGCCTTGGGCAAGGA | 63893 |
| rs554692509 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451934 | GCATCACCCCAAAAA[A/C]CATACGGGAGTCAGA | 63893 |
| rs554750741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446432 | AAAGTTCCTCTTAGT[A/G]TAACAGGAAAATGAA | 63893 |
| rs554812028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440225 | CTATGGTAAAAAGAA[C/T]GCACAGTCTCTCATT | 63893 |
| rs554815973 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403969 | TTAATTATAACCAAT[A/G]AATAAAACAGAAATC | 63893 |
| rs554834643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397425 | GGGCTAGAACTGGGT[C/G]GGCTCTCTCCTTTCT | 63893 |
| rs554849357 | in-del | -/ACAATG | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76403744 | TACCATTCTCTGAAA[-/ACAATG]AGGCTTCTTGGAGAA | 63893 |
| rs554853500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439396 | CTGAAACCCTTTCAG[G/T]AGGTCCAAAGTCAAA | 63893 |
| rs554876093 | snp | A/G | 6.68405e-05 | 0.00578064 | missense | UBE2O | GRCh38.p7 | 17:76396553 | TCCATCAGCCCGGCC[A/G]TGGGGGCAGCCATGG | 63893 |
| rs554914891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425953 | GTTTTGGTGAAGAAC[A/G]ACTCCTTCTATCTCC | 63893 |
| rs554933555 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433528 | GATGACCGTACAACC[A/G]TTTGAGTATACTAAA | 63893 |
| rs554958445 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76450770 | CAGGTTACAGGCATG[C/T]GCCACCAAGCCCAGC | 63893 |
| rs554965589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407499 | CAGGACAGGAGAATC[C/T]AATGCAAGGGGGGCT | 63893 |
| rs554967555 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76415055 | TGGGTATCACTACCT[A/G]ACCAGTGGCCCCGGA | 63893 |
| rs554984378 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431742 | AAACCAGGAGTTTGG[A/G]ACCAGCCTGGGCCAA | 63893 |
| rs555033464 | snp | C/T | 5.05531e-05 | 0.00502733 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402079 | CGAGTCGCTGACGTG[C/T]GGGCAGACGTCGTAG | 63893 |
| rs555117871 | snp | C/T | 3.41151e-05 | 0.00412994 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396156 | CAGTACGGAGAAGAC[C/T]TCGCCCTTGGCGCTG | 63893 |
| rs555128327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438897 | CATGCACACCGAGGG[C/T]ACAGAGGACACAACT | 63893 |
| rs555133463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442185 | ACAATGCACGTAGTC[G/T]GCCTGGGGAGCCCGC | 63893 |
| rs555154059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76399386 | GCACGCACACCGAGG[C/G]GACGCGCACTCTGCC | 63893 |
| rs555189898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76433061 | GATTTACCTACCATA[C/T]GACCCAACAACTCCT | 63893 |
| rs555197097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436458 | TAAGGCAAATAAGAG[C/G]ATGACTCCAGCAATT | 63893 |
| rs555206544 | snp | C/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452486 | ATGTCTTAGAAGTCC[C/G]CTCAAGTCGGGAAGC | 63893 |
| rs555243997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393336 | GTGGTGTGATCTTGG[C/T]TCACTGCAACCTCTG | 63893 |
| rs555249750 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419943 | CTCGGCCATGGCCCT[C/T]GGGACCCTGGTGCTC | 63893 |
| rs555253031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433527 | TGATGACCGTACAAC[C/T]GTTTGAGTATACTAA | 63893 |
| rs555329719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76435135 | GTGAGTCACCACGAA[C/G]CAAACGGGAAGGTCA | 63893 |
| rs555352831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441952 | TGATTCATTTGCAGT[C/T]GGGTGGGGCATTCTT | 63893 |
| rs555367680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405135 | CACGGAGGAGGCTGT[A/G]GCCCAGAGGTCGTGC | 63893 |
| rs555387632 | snp | C/G | 0.000399281 | 0.0141238 | missense | UBE2O | GRCh38.p7 | 17:76398916 | GAGGTCGTTGGAGCG[C/G]ATGTTGCATTCCACG | 63893 |
| rs555393130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428532 | CTCTTCTTTCTGAGT[A/G]TATTTGCCATGTGCT | 63893 |
| rs555430655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405705 | GCGTTTGGCTAGCAG[C/T]ATCTTCACAGACCGC | 63893 |
| rs555454438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429060 | GCGCATGCCACCATG[C/T]CCGGCTAATTTTTGT | 63893 |
| rs555548194 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76393714 | GGTTTGAACTCCATG[C/G]GGGAGGTTGGGAGAC | 63893 |
| rs555652999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430233 | GTCCTTGTGGGTTTA[C/T]ACATCTAAAAACAAT | 63893 |
| rs555653357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423459 | AGCACTTCGGGAGGC[C/T]GAGGTGGGAGGATCA | 63893 |
| rs555737800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76432108 | GCACATGTGCCCCTC[A/G]GCAGACAGCCACACA | 63893 |
| rs555807327 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441609 | GTGCAATTCAAAAGA[C/G]AGTCCCAGCCAGCAG | 63893 |
| rs555847866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422168 | CGTGGCCTCTCTCTC[C/T]GGCTTTTCCTCAATG | 63893 |
| rs555909292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416192 | TGTGTGTATATGTAT[A/G]TGTGTATATGTGTGT | 63893 |
| rs556006566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419778 | CTTCCAGGCAGGAAG[A/G]CCATGCTGTGGCCCT | 63893 |
| rs556017929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450928 | CCCGGCCGTTGTTTT[C/T]GATTTAACTCCAAAA | 63893 |
| rs556036064 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401492 | TGCTGTGTGTGTCCA[C/T]GTACTATTGTAACTA | 63893 |
| rs556067944 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76414728 | AGTGAGGGGGAAGGA[C/G]TGCAGAGCTTGGCCT | 63893 |
| rs556100264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76411353 | TGTCCCTGTAGGAGC[A/G]GATGGCTCCTAAAGG | 63893 |
| rs556132272 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389078 | CCATTTTGGCTTAGC[A/G]TCCAGGAGTTGTGGC | 63893 |
| rs556244293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406334 | CTCAAACCTGGGGCA[A/G]CTCCTCTATGGTTCT | 63893 |
| rs556365782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415114 | GGTCCTGTGGCTGCC[A/G]GGCATCCCTGAGAAC | 63893 |
| rs556382858 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76400803 | CACCTTGCTCAGCCT[A/G]TACAGGCTGGGCTGG | 63893 |
| rs556385764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76400718 | AACCACGGCCCCCAC[A/C]CAATGCCCAGGACCA | 63893 |
| rs556424572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76401268 | GCCCACTCACACACA[C/T]GCCCCACACGCCCTA | 63893 |
| rs556434690 | snp | A/C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415007 | AGAAAAGTGATCAGC[A/C/G]TGATTCCATGTTCTG | 63893 |
| rs556492216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443739 | TGGAAGTCACCTAAA[G/T]ACAGGTACCAGATGC | 63893 |
| rs556551621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437730 | GGCTCAATGTCAATT[C/T]TTTTACTTTCGACAA | 63893 |
| rs556563657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394697 | TTGGAAGGAGACCCA[C/T]TAAACTTCCAACAAT | 63893 |
| rs556611777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455190 | CAACACTTTGACTGC[A/G]CCTGAAATCCCAACA | 63893 |
| rs556621595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413906 | GAAAATGGGGCCTCC[C/T]GTTGGAGCTGGACTC | 63893 |
| rs556759579 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76453047 | GCCGGCGCCGGGACG[G/T]GGGCTGCGGCTGGGG | 63893 |
| rs556780516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76398027 | GGTAAATGTAACCAG[C/T]GGCAGCTCAAGAAGC | 63893 |
| rs556791201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444414 | TAAAAAGCCGAGTGT[A/G]TAGTTCCAGCTGCAC | 63893 |
| rs556850686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438320 | TGTTTATTTAAAAAT[A/G]GTTAAAATGGTAAAT | 63893 |
| rs556868389 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428611 | TTTTCTCTTTGCTTT[A/C/T]TCTGGCCTCTACCTT | 63893 |
| rs556960900 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76409689 | GTGAGCCACCGCCCC[C/T]GGCAAACACACACCA | 63893 |
| rs556985836 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450185 | TGGTCTTTCCTTTAC[A/G]GCATACTATCACCTT | 63893 |
| rs557010753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76435832 | TCCCGCAAAGCTCAG[G/T]GACACCCCGGCACAG | 63893 |
| rs557059010 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423766 | GCCAAGGGAGAGCCT[A/G]AAGATTCAGGCCCAG | 63893 |
| rs557120914 | snp | C/T | 1.64925e-05 | 0.00287158 | missense | UBE2O | GRCh38.p7 | 17:76396224 | ACAGCACCGGGGTTT[C/T]GCTGGGCCACTCAGC | 63893 |
| rs557265545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441725 | ATGGCATGTGGCATT[C/T]ACCTTGGAAAAGTGC | 63893 |
| rs557269988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434203 | AGGATCCCTTCCAGT[A/C]TTACCACTATAGACC | 63893 |
| rs557340412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442929 | ATGCAGGCACAGGAT[A/G]CAAGAGGCCTCTCAA | 63893 |
| rs557349184 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402100 | GACGTCGTAGAGCTT[A/G]GCGCCATCTTCCGTG | 63893 |
| rs557361383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408802 | GTGAACAAAACTAAA[A/C]CTTGGAATAAACCCA | 63893 |
| rs557373039 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410594 | AAGTAGGAAAGCAAT[A/C]AAATGGTAAGTGAGG | 63893 |
| rs557399312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76439482 | AAAGTCTGCAGTGGA[A/G]TTTTCCAGAGGCTAC | 63893 |
| rs557537765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437064 | TGAGGCAGGAGAATC[A/G]CCTGAACCTAGGAGG | 63893 |
| rs557587325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426618 | CTTAAAATTGGAACA[C/T]GTCTACTTGACTCAG | 63893 |
| rs557640000 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445650 | CCTGGATTGAAGGAC[A/G]TTAAATCCTCAATCA | 63893 |
| rs557644712 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76421193 | ACTCACAGCTACAGT[A/G]AGCTCCCTAGAGCTG | 63893 |
| rs557740628 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76399394 | ACCGAGGGGACGCGC[A/G]CTCTGCCTGGCTTCA | 63893 |
| rs557743742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436477 | ACTCCAGCAATTTTT[C/G]TTCGGTGCTGGATTG | 63893 |
| rs557837992 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76392740 | GGTGGATCACTTAAG[G/T]TCAGGAGTTCAAGAG | 63893 |
| rs557849570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416928 | GTGAGACAAAGCTGC[A/G]GCTGGTCACATGGAG | 63893 |
| rs557849575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76423314 | AGCCCAGGAATTCGA[C/T]GCTGCAGTGAGCCCT | 63893 |
| rs557866434 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76437581 | ACAGTATGTGGCTGA[G/T]GTTAATATCTTTTTT | 63893 |
| rs557866756 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76429122 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCGT | 63893 |
| rs557926648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430838 | CTCACACCACTGATA[C/G]CTCTGACCCTGATGA | 63893 |
| rs557999442 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432160 | GCAGCAGCCAAGAGC[A/C]TTTGGAAACTCAAGG | 63893 |
| rs558011635 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76448322 | CTTGGTTAACCTTAT[A/G]TAACTTCTTCACATT | 63893 |
| rs558045861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418375 | GACACCCTCTTCCAG[A/G]AGCCATGCCTTACAA | 63893 |
| rs558074783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442199 | CTGCCTGGGGAGCCC[A/G]CGACGGAAGTTGCCA | 63893 |
| rs558076602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448782 | CAGAAGGACCCACCA[C/T]GTCTAGCCAGTGCTC | 63893 |
| rs558085765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454626 | TCAGGAGTTCAAGAC[C/T]GCCCTGGCCAACATG | 63893 |
| rs558107257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418846 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACCGCG | 63893 |
| rs558114391 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76412040 | CAGAAAAGGTCCAGC[A/G]TCATGCCAAGTGCCC | 63893 |
| rs558175602 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE2O | GRCh38.p7 | 17:76405729 | AGACCGCACACACCT[C/T]CGACCAGCACCCAGA | 63893 |
| rs558252686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415213 | TGCCATGTTAGTTCA[C/T]GGAATGAGGACCCAG | 63893 |
| rs558254633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420868 | GTGAGTTGGCAGGGA[C/G]GGCCTTGTCACTCAC | 63893 |
| rs558288197 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453773 | GCTGGTGAAGGAGGC[C/T]CAGAGAAAGGTAACA | 63893 |
| rs558317936 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76415828 | GTGTGTGTGTGTGTG[C/T]GCATACACATATATG | 63893 |
| rs558430854 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401852 | TTGCACTCCAGCCTG[G/T]GCGACAGTGAGACTC | 63893 |
| rs558454805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439526 | ACGTCACTGCTCTGA[C/T]GGCCAATAGAATGTA | 63893 |
| rs558495760 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389673 | AACAAGATACCGACT[C/T]GGTTCCAAATGCCAC | 63893 |
| rs558537106 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76436017 | TTTGGGAGGCTGAGA[C/T]GGGCGGATCACCTGA | 63893 |
| rs558609341 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76446364 | GCTGGCCCCCAACAG[G/T]TTCCACTGGATTCCA | 63893 |
| rs558641233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76400818 | GTACAGGCTGGGCTG[A/G]GGCACATCTGTCTTT | 63893 |
| rs558666316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413985 | GAGGATGTGAATGGT[C/T]AGTAATTCCGGCTGG | 63893 |
| rs558679764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401313 | GCTCCACATCAGCAC[A/T]TCCCAAACCCTGGGT | 63893 |
| rs558686987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449736 | ACAGCCTGGCCACCA[C/T]GGAGAAACCCCGTCT | 63893 |
| rs558695968 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419292 | CTATCTCAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 63893 |
| rs558754036 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439436 | TAACAAGACCAAGAC[A/G]TTATTTGCCTTTTTT | 63893 |
| rs558768109 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76437150 | GAGACTCCATCTTTA[-/A]AAAAAAAAAAAAAAA | 63893 |
| rs558803135 | snp | A/G | 1.77055e-05 | 0.00297531 | intron-variant | UBE2O | GRCh38.p7 | 17:76395940 | TGGCTGGACAGGTGA[A/G]CACACCCACAGACTT | 63893 |
| rs558824071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76402831 | ACTGGACCGGTTGGC[C/T]ACTAGCCCTAAACAG | 63893 |
| rs558831891 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76419919 | GGCATGCCTGCTTGG[-/C]CCCCATTCCTCGGCC | 63893 |
| rs558871560 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390591 | GGGTCTGCAGGGAAC[C/T]GGCCCAGAGAGCCCC | 63893 |
| rs558948760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397618 | CTGGGAGAAGCGAGG[C/G]TGGTGGGCCAACTGC | 63893 |
| rs558955750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76414613 | TGCTGCTGCATCACC[A/G]CCTGGAAACTCGGCT | 63893 |
| rs558957455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76432232 | ATTTCGGCACAACCA[C/T]GTCTTAGACCCGTCA | 63893 |
| rs558967403 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389105 | TGGCACCTGTCCACC[A/G]CCAGGTGCTATGACG | 63893 |
| rs558975158 | in-del | -/TCCTGAATTGGG | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76404527 | CAATGCAAGATGTGT[-/TCCTGAATTGGG]TCCTGGATCCGCAAA | 63893 |
| rs559062934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443811 | GAGATAAAGAAAAGA[C/G]AGGTCTTTGGAAAAG | 63893 |
| rs559072984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403779 | AATGGTTGATTCTGG[A/G]GCTGGATCACAAAAA | 63893 |
| rs559103219 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416101 | TACATACATGTATAT[A/G]CGTATGTGTATACAT | 63893 |
| rs559202587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438483 | CCGGCTCAGCTGTAC[A/G]TGCAAGGCTGTGAAA | 63893 |
| rs559202646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444850 | GAGCACATGAATACC[A/G]GGATGCTTTCAGCAC | 63893 |
| rs559234991 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416372 | TGGGAATCATCTGAA[A/C/G]AAGTTCCCCAAATGA | 63893 |
| rs559235926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432947 | AAGCATTGGTGAGCA[A/T]GTGGAGAAACTGGAA | 63893 |
| rs559263849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438887 | TAGGTGACGCCATGC[A/C]CACCGAGGGCACAGA | 63893 |
| rs559299317 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423995 | TCACTGCAAGCTCCA[C/T]CTCCCAAGTTCACGC | 63893 |
| rs559335939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422301 | GGCATGGGCAAAGGG[C/T]GGCTCACTTTAACCT | 63893 |
| rs559411615 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76408806 | ACAAAACTAAACCTT[A/G]GAATAAACCCAATCC | 63893 |
| rs559448284 | snp | A/C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421241 | ACACTGCAGAAAGAA[A/C/G]TGACGGCCTGCTGTC | 63893 |
| rs559456656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441005 | AGAGAACCTGCATTC[A/G]GGCAGCACAAACTGG | 63893 |
| rs559458632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434470 | GTAAAGGACACGCCA[A/G]TAGTCCTGCCATGAA | 63893 |
| rs559461645 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449468 | TAATCCCAGCTATGC[A/G]GGAGGCTGAGGCACA | 63893 |
| rs559464572 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76402257 | ACCATCAACTCAGCC[A/C]GAGGTAGTACAAGAA | 63893 |
| rs559478620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433773 | TGGCCTGTAATGCCA[A/G]CACTTTGGGAGGCCA | 63893 |
| rs559521771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76435316 | AGTGAAAATGGTAGG[A/G]GGGAGACAAACATTT | 63893 |
| rs559553807 | snp | A/G | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390003 | AGGAGAGCCCCCGCC[A/G]GCCGTCCCCTTCGGA | 63893 |
| rs559561218 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448323 | TTGGTTAACCTTATA[C/T]AACTTCTTCACATTA | 63893 |
| rs559589674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76392781 | AACGTGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 63893 |
| rs559710201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430484 | GCTCCATTTTCTACA[A/C]AATGGGTGGTCTTTT | 63893 |
| rs559780038 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452423 | ACCTGAGTCCCCACG[A/G]GAGTCGGTCCACGTC | 63893 |
| rs559818584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76409779 | CTGTGCCTCCTCTGG[A/G]AACAGGAGCAGCAAA | 63893 |
| rs559836652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446540 | GAAGGTGCAAAGAGG[C/T]CTCTAATGTCCTAAA | 63893 |
| rs559901597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415574 | CTTTGAGAGGGCAAG[A/G]CGGTTGGATCACTTG | 63893 |
| rs559901691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421238 | GAAACACTGCAGAAA[A/G]AAGTGACGGCCTGCT | 63893 |
| rs559934957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76409062 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATCCT | 63893 |
| rs559995300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403141 | CGAGAGCCAAGTCCC[C/T]CATTGTTGGAGAAGG | 63893 |
| rs560092638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410742 | CCGGGGAAGCTCACC[A/G]GGGGCCTCTCCTGCC | 63893 |
| rs560129128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406519 | AAGGAGAACTGAGTC[A/G]CCGAAAAAGGAAGAT | 63893 |
| rs560154158 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389183 | CTCTGGAGACTACAG[C/G]TGCTGGGAGGCTGCT | 63893 |
| rs560163473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443327 | AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 63893 |
| rs560245904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76417913 | TGATGGTGCTGTTTC[C/T]GCTGGTATTTGAGTC | 63893 |
| rs560254118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441992 | GAGAGCCTCGTTCGT[A/C]CTTAGCCATCCTCCT | 63893 |
| rs560294182 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405947 | TTTGCTTTGCGTTCA[A/G]TCTTTTTTCTGCCCT | 63893 |
| rs560314175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76436043 | CCTGAGCTCAGGAGT[A/G]TGAGACTAGCCTGGG | 63893 |
| rs560360509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76447946 | ACCCAGCTACACTTC[C/T]GGTTATTCCATCCGA | 63893 |
| rs560366096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413419 | AGTGGGTTATAGAAC[C/G]AATTTAGTGGGTCAT | 63893 |
| rs560371330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449756 | AAACCCCGTCTCCAC[C/T]AAAAATACAAAAAAT | 63893 |
| rs560377870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76436569 | CCCGAGAGCCTAGAC[A/G]ATGCCTCCAGGCCCC | 63893 |
| rs560429295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76414039 | AGCAGTTGACCATCA[C/T]GTGGCTGAGCCCTGA | 63893 |
| rs560442396 | snp | A/C/G | 9.98947e-05 | 0.00706677 | intron-variant | UBE2O | GRCh38.p7 | 17:76398996 | CCACTGCCACCCTGC[A/C/G]GGTGCAGGCCAGTCA | 63893 |
| rs560466070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76406978 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCATCC | 63893 |
| rs560499619 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453369 | GAATCCACTAAGAAG[A/G]GGCGAGACCAGTGAG | 63893 |
| rs560527704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415413 | GCCAGGACTCCAGAG[C/T]CTTTGTTTTGCTCAC | 63893 |
| rs560594003 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429690 | AGGAGCCACTACATA[C/T]TGGCAATGGCAGGTC | 63893 |
| rs560613224 | in-del | -/GGC | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453410 | AAGGGAGCGAGAAGG[-/GGC]GGGGACCCGGGAGGA | 63893 |
| rs560675810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448410 | TTCACGTGCCATGAT[A/G]CTACACCTAAATAGC | 63893 |
| rs560787739 | snp | G/T | 1.64841e-05 | 0.00287085 | missense | UBE2O | GRCh38.p7 | 17:76399474 | GCTTGAAGTCTCGAG[G/T]GATTTTATTCTTCTT | 63893 |
| rs560813438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433820 | TGAGGAAAGGAGTTT[A/G]AGACCAGCCTGGGCA | 63893 |
| rs560821276 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392998 | CGTGATGGCTCACAC[C/T]TGTAATCCCAGCACT | 63893 |
| rs560881090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76451188 | TCAAATAGATGGGTG[A/G]TGAAAAACATTCTTA | 63893 |
| rs560884922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76402937 | GGTGGTGGGGCTGCC[C/T]GGAGGGAACGGGGTG | 63893 |
| rs560972710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76396940 | GGGCTCATGAGGCCT[C/T]GGCAACCTCATTCCA | 63893 |
| rs561111774 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390039 | CCTGCAGTTTGTAAG[C/T]GAAGGGCTGACAGTA | 63893 |
| rs561127506 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439435 | ATAACAAGACCAAGA[C/T]GTTATTTGCCTTTTT | 63893 |
| rs561173963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76435984 | CCGTGCGGTGGCTCA[C/T]GCCTGTAATCCTAGC | 63893 |
| rs561191313 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76411021 | AAATAAAGAAGCTAC[-/T]TTTTTTTGGTGTGGT | 63893 |
| rs561212455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76395491 | GCCACTGCGCCCGGC[C/T]GAGAAAGTAATTTTT | 63893 |
| rs561255160 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76424933 | TGGAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG | 63893 |
| rs561262447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76414781 | CTCTGCAGATGCTGC[A/G]GTGTTTGATAAGCAA | 63893 |
| rs561296589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76400911 | CCAGATGCTGAGGAG[C/T]GGGGCTCAACCCTCA | 63893 |
| rs561330563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76431445 | TGCTTGAATCCGGGA[A/G]GCACAGGTTGCAGTG | 63893 |
| rs561332324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438598 | TCTCTACCTCACTAC[C/T]CTAATAATTGAAAGC | 63893 |
| rs561399662 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417129 | CTCCAGGCCCTTCCG[A/G]CTACAGCTCCAGAGC | 63893 |
| rs561408179 | snp | C/T | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389381 | CACTGCCACATGCCT[C/T]CCCTGGCAACAAACA | 63893 |
| rs561441847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420465 | GCCAGAAATGTTACA[A/G]ACTCGCCCACATCTT | 63893 |
| rs561468426 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE2O | GRCh38.p7 | 17:76423158 | TGAAGAGCAGGAAAA[G/T]GAGGAAGAGGTAGGT | 63893 |
| rs561525511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425412 | AAAACAGGCAGTCCC[C/T]CATCTTACCCTCTCA | 63893 |
| rs561532906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448885 | AAGGGGCAAGCCTCC[C/T]CTAAGGAGATCCATG | 63893 |
| rs561591248 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76412969 | GCCGAGATTGCGCCA[C/T]TGCACTCCAGCCTAG | 63893 |
| rs561611604 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426082 | ATCATGGTTCACTGC[A/G]GCCTCAACCTCCTGG | 63893 |
| rs561853895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422347 | GAGCTCAAGTCCCAT[C/T]TCTCCTCCAGCAAGG | 63893 |
| rs561897745 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452548 | CCTGGCTGGCGTGTG[A/C]GCCCAGAGCTGCTGC | 63893 |
| rs561954420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454088 | TAGCTCCTTCGATAA[A/G]CTTAACCATTGTTGT | 63893 |
| rs561958124 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime | AANAT, UBE2O | GRCh38.p7 | 17:76453154 | CATAACTGCTCTGCG[C/T]GAGTCTCGGGCGGCG | 63893 |
| rs561995704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421585 | GGTCAGGCTGGTCTT[G/T]AACTTCCGACCTCAG | 63893 |
| rs562017870 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76402432 | AACAGAAATAGGCCA[C/T]GGCAGATAAGGAGAA | 63893 |
| rs562032247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76417776 | CGAGACAGGAGGAAG[C/G]GAAGAGGAGCAGGTG | 63893 |
| rs562105022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421274 | CGCTCATGGCTGACA[C/T]CACATGGTCACCATT | 63893 |
| rs562139965 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76424866 | TTTTTTTTTTTTATT[A/T]TTTATTTTTTTTTTT | 63893 |
| rs562249076 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438621 | TTGAAAGCTTTATTA[C/T]TGTTCTCTTAGGTTC | 63893 |
| rs562301619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449861 | GGAGGCAGAGGTTGC[A/G]GTGAGCCGAGCTGGC | 63893 |
| rs562310816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76410640 | CAGGGCAGAGGGCAA[C/T]GTGGCAGGAGGCTGG | 63893 |
| rs562329976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446590 | GAAGGGAACAGAAAC[C/T]GAAATTGAGGTGGAA | 63893 |
| rs562346084 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76396034 | TAGCTGGGGTCTGGC[A/G]AGGGGACTAACCACC | 63893 |
| rs562359312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450337 | GCTAATCAGTCACCT[C/G]TATCTATAGCTCATG | 63893 |
| rs562363813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76443991 | TTTGGGAAGCTGAGG[C/T]GGATGGATCACCTGA | 63893 |
| rs562389342 | snp | C/T | | | missense | UBE2O | GRCh38.p7 | 17:76398500 | CCACTCGGCCTCAGC[C/T]TGAACCACTTCACCA | 63893 |
| rs562391128 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76440452 | CTCACCTCAGCCTAC[G/T]GAGTAGTTGGGACTA | 63893 |
| rs562424116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397665 | CTGTGTGGAATGCCT[A/G]CCTTTCCCCTCACGC | 63893 |
| rs562425660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444604 | ATTCACTAGTCATTT[C/G]TGACCTTCAGGGGAG | 63893 |
| rs562524341 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76405385 | GGGGAGACCCAGCCC[A/G]GGCAACCCCAGCGCA | 63893 |
| rs562562136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419020 | CTGCCACGGTGACTC[C/G]CGCTGTAATACCAGT | 63893 |
| rs562622635 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76414126 | ACAAATGGCCAGGGG[C/G]CCTCACATGCTTGGG | 63893 |
| rs562658295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394999 | TCCTGCCTCAGTCTC[C/T]CGAGTAGCTGGGATT | 63893 |
| rs562701277 | snp | A/G | 5.00271e-05 | 0.0050011 | intron-variant | UBE2O | GRCh38.p7 | 17:76400316 | GTTGGGGAAGAAGTG[A/G]GGGTGAGCTGGGCTG | 63893 |
| rs562755842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430044 | AGGCCCAAACCTTAT[G/T]CCCACCTTGAGTGCC | 63893 |
| rs562788982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401552 | GTGGAACCTTAAAGG[A/G]TGAGAAAAAAAAGCT | 63893 |
| rs562823673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454984 | ATACAAAAATTAGCC[A/G]GGCGCGGTGGCAGCC | 63893 |
| rs562846593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438636 | CTGTTCTCTTAGGTT[C/T]GATAGATTTCAGATT | 63893 |
| rs562875305 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76424178 | CTCCCAAAGTGCTGG[C/G]ATTACAGGCGTGAGC | 63893 |
| rs562880882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76412413 | TGACCCCCCATCTCT[C/T]ATTGTCTGAGCTGGG | 63893 |
| rs562900423 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433128 | CATTCACACAAAAAC[A/G]TGGACTTGAATGCTT | 63893 |
| rs562971764 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76411748 | TGGAGGGCAGTGGCG[C/T]AAGCAGGGTTCACTG | 63893 |
| rs562990460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403018 | CATGGACACAGGACA[A/C]CTGGCAAAGTAGGCT | 63893 |
| rs563061326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397006 | CCTAGGTCTCTGGGA[G/T]AGGCCCTTCACCTGT | 63893 |
| rs563142675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393909 | CTCTTATCGGTGCCA[C/T]CCTGGGAGCCTCCAG | 63893 |
| rs563212664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428018 | TCCTGCTTTGCTTTC[A/G]GTTCTCTGTTTTTCT | 63893 |
| rs563229878 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451998 | CTTCGGGTTTCCAAA[C/T]TGGTGACTCCCCTCT | 63893 |
| rs563275310 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442271 | TTCCTAGTATTAGGA[C/T]GCCCATACGTCCCAG | 63893 |
| rs563281667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421634 | CCTCCCAAGGTGCTA[C/G]GATTACAGGCGTGAG | 63893 |
| rs563302663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421522 | AGGCATGTGCCACCA[C/T]GCCCAACTAATTTTG | 63893 |
| rs563344680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434456 | TCTTCCTGGAAACTG[G/T]AAAGGACACGCCAAT | 63893 |
| rs563395360 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444705 | GAGGCAGACATCCAT[C/T]TCCCCCAGTACAGTG | 63893 |
| rs563453678 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390879 | GAGGGGTGATTCCGG[C/G]GGGGAGTGAGCAGGC | 63893 |
| rs563614953 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389857 | GAGTTTTTTTTCCAA[C/T]CTTAAATATTACATA | 63893 |
| rs563655515 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76395519 | TTTTAAAGGAGGGAG[G/T]AAAGAAAGAACCATC | 63893 |
| rs563708121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432370 | CAAAAGAAATAGATT[G/T]TATGGTCTCCGCCTT | 63893 |
| rs563744644 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389279 | AAGTACAAAAGGCAT[A/G]CAAGCAGGTCTGGCA | 63893 |
| rs563809670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426059 | CTAGGCTGGAGTGTA[A/G]TGGTGTGATCATGGT | 63893 |
| rs563846487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415898 | ATGTACATACACGTA[C/T]ATACAAATATATACA | 63893 |
| rs563866108 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76420564 | TTTCATGACCCACCC[A/T]GGAATGACTATGTCA | 63893 |
| rs563879487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393010 | CACCTGTAATCCCAG[A/C]ACTTTTGGGAGGCCA | 63893 |
| rs563965005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415501 | CCAATTGGAACCATG[C/T]TGCCATTCAAGTGTG | 63893 |
| rs564008781 | in-del | -/GAG | 0.00312405 | 0.0393988 | intron-variant | UBE2O | GRCh38.p7 | 17:76405596 | AAAATACAGGTGTGA[-/GAG]GAGAATGGACTCTGA | 63893 |
| rs564122591 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453361 | GCAGGATGGAATCCA[C/T]TAAGAAGGGGCGAGA | 63893 |
| rs564145226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455000 | GGCGCGGTGGCAGCC[A/G]CCTGTAATCCCAGCT | 63893 |
| rs564204915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423579 | GTACCTATAGTCCCA[A/G]CTACTTGGGGGGCTG | 63893 |
| rs564245373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76406106 | CCTCCTGACCAGCTG[C/T]GGCCTGCACCTTATC | 63893 |
| rs564358804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76447823 | GCCTCTTTGGTGCAG[C/T]ATCACCCTCTTTCTC | 63893 |
| rs564360475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441334 | ATGAAACTTCTTAGC[A/C]ACAGCAGTGCATTAA | 63893 |
| rs564385396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76416209 | GTGTATATGTGTGTG[C/T]ATATGTATGTATATG | 63893 |
| rs564405274 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453298 | TGCAGTTGCTAGGAG[C/T]CACCGCCTCGTCGCT | 63893 |
| rs564415881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442641 | GCACAATTGAGTTGG[A/G]GAAAAGCAGTCAGAT | 63893 |
| rs564428449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413338 | TTCTGAAAAAGCTGC[A/G]GAAATCGTAGAATGG | 63893 |
| rs564448486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448996 | GGCCACTAGCTCCTT[C/T]TGAGTCCTTAAGAGG | 63893 |
| rs564536724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419860 | GCGTGGCTCTACCCA[A/C]GCGGAAACCTCAGAG | 63893 |
| rs564564648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410148 | CTTAGAGAGCCACAG[A/G]GAGGGCTTGAGATTC | 63893 |
| rs564653914 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76406232 | CGCACAGCTGGCAGC[A/G/T]GCCACTGCCTCCTGC | 63893 |
| rs564743299 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445151 | CTCTTTTTAAGGGTG[A/C/T]CTGCAGGAAATCTCT | 63893 |
| rs564743855 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76449969 | AAACCATCACTACTG[C/T]AGTCCCAGCTACCTG | 63893 |
| rs564785435 | snp | A/G | 3.3065e-05 | 0.00406588 | missense | UBE2O | GRCh38.p7 | 17:76398968 | TCGGCTGAGGTCATC[A/G]TGGTCACCACCTCCA | 63893 |
| rs564785545 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76435607 | CACTGGTCAGGTGCT[A/G]TGCTGAGCCCTCTCG | 63893 |
| rs564790762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407239 | CTGTGAGCTGCAGGG[A/T]GAAGACCCCTGAAAG | 63893 |
| rs564818512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76392517 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 63893 |
| rs564871397 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404998 | TATGCTGGGGTTGGG[C/G]AAGGGCACGTCCTGA | 63893 |
| rs564918605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408131 | TACCCTCCCATCTGT[A/G]AGCCACTCCACTGAA | 63893 |
| rs564953553 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76392398 | AGCCTCCCAAGTAGC[C/T]GGGACTACAGTGTGG | 63893 |
| rs564966472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76400363 | GCAGTGTTCTTAAGC[C/T]TCCCCAGGCATGTGA | 63893 |
| rs564977178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450409 | ACAAACCTATTCTAA[A/G]TCCTAAAAGAACTAT | 63893 |
| rs564980712 | snp | A/G | 0.000107465 | 0.00732947 | intron-variant | UBE2O | GRCh38.p7 | 17:76402176 | GGGGACACAGTGAGT[A/G]CCAAAAAGTTGCGAT | 63893 |
| rs565015606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407665 | AGCACCCTTGGGAGT[A/G]CAGGGGAAACCGAGG | 63893 |
| rs565053012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394126 | TGCCTAGCCCTGTTC[A/C]AGGGTTGTGGCTACT | 63893 |
| rs565079189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401607 | AATACTGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 63893 |
| rs565101643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395617 | GTGGGTGAGTGTCCT[C/T]GCAGGTGCCAGTCAG | 63893 |
| rs565127991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76424255 | CTTTTGTTGCCCAGC[C/T]TGGAGTGCAATGGCA | 63893 |
| rs565129292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76435765 | GCCTCTCAGTCCAGC[C/T]CTATGCTCGGGAGCC | 63893 |
| rs565193567 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389432 | AGGGTGTGTGTGAGG[G/T]ACACAAAGGCAACGG | 63893 |
| rs565267180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76406392 | TCTGTGTGTGTCCAC[C/T]TCCGAGACCCCAAAC | 63893 |
| rs565285327 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76443293 | GGGGAATATATATAT[A/T]TATTTTTTTCCTCGA | 63893 |
| rs565298849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76397212 | GCTGGGAACATATGA[C/G]AAGAGGGGACATGTA | 63893 |
| rs565344943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437428 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGATTC | 63893 |
| rs565384919 | snp | C/T | 5.00455e-05 | 0.00500202 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391000 | GGCAGCCCGGAACTG[C/T]GTCAGGACACCCCGG | 63893 |
| rs565405672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420943 | CTTTCTTCAGCCCCC[C/G]ACATCCCTGCAATTA | 63893 |
| rs565408131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437820 | GGACTTTCTGTATGA[A/T]CTTTGAAACTGTTCT | 63893 |
| rs565484192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76431382 | TTAGCTGGGCGTGCT[C/G]GTGCACGCCTGTAAT | 63893 |
| rs565545175 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76424875 | TTTATTTTTTATTTT[A/T]TTTTTTTGAGACAGA | 63893 |
| rs565588752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76416113 | TATGCGTATGTGTAT[A/G]CATATATACATATAT | 63893 |
| rs565633257 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76412675 | ACTATAGTTCAAGAC[-/AG]GGGTCACGTGTGTTA | 63893 |
| rs565651574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410358 | GTCTGGAGACACTTT[C/T]GGTGGTCATAAAGGG | 63893 |
| rs565653740 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448589 | TCAAACCTGGTGAAA[A/C]CCTGAATGTCATGGC | 63893 |
| rs565667831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421393 | TTTTTTTGAGACGGA[A/G]TTTCGCTCTTGTTGC | 63893 |
| rs565681306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76434072 | CCTCCTATAGACTTT[C/T]ATTTCCTAAGAAAGA | 63893 |
| rs565753521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76417773 | AGGCGAGACAGGAGG[A/G]AGGGAAGAGGAGCAG | 63893 |
| rs565789108 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76430683 | ATGAGTTTATTTACT[A/G]ATTTCAGATTTGGGT | 63893 |
| rs565855719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421722 | CACCATTTGAGATCC[A/G]TTACAACTGGTAACT | 63893 |
| rs565890043 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419011 | AACTTCTGACTGCCA[C/T]GGTGACTCGCGCTGT | 63893 |
| rs565892230 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452219 | GTGGCTTCACCATAA[C/T]GCAGCCTGTAAGCTA | 63893 |
| rs565953262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446401 | CCCATGGTGGGTTAA[A/G]TAGTAAAAAATAGAA | 63893 |
| rs565980519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403653 | ATACATATAATACAT[A/G]TGTATTTCCTAGTGT | 63893 |
| rs566020116 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76438154 | ATCCACTGCTTTTAG[-/A]AAAAGGTTTTTCTAA | 63893 |
| rs566055693 | snp | A/C/G | 6.60954e-05 | 0.00574838 | missense, synonymous-codon | UBE2O | GRCh38.p7 | 17:76396504 | CTCTTTCAACTCCCG[A/C/G]AAGCTCTTGGGTGGC | 63893 |
| rs566069041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414646 | AGCTCGCCAGCTTGC[G/T]GGAATGGCCTGGAGG | 63893 |
| rs566094554 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453619 | GTTGGGGAGACAAAA[A/C]AAATACACATTAAAT | 63893 |
| rs566116985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408633 | CTGAGGCAAGTGGAA[A/G]GCAGCAATGGTGGCC | 63893 |
| rs566132193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76415003 | AGGCAGAAAAGTGAT[C/T]AGCATGATTCCATGT | 63893 |
| rs566145057 | snp | A/G | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455128 | TGAGATTCCGTCTCA[A/G]AAAAAAGTAACTCTA | 63893 |
| rs566155940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445668 | AAATCCTCAATCACA[C/G]AGTATAGCTAACGAA | 63893 |
| rs566157257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454439 | GCAGTGAGCCCAGAT[C/T]GCGCCACTGCACTCC | 63893 |
| rs566162647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450733 | TTCAAGCAATTCTCC[C/T]GCCTCAGCCTCCCGA | 63893 |
| rs566261571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401999 | TCCAGGTCTTTGCTA[C/T]GAAGTCCTCCTTCCA | 63893 |
| rs566292968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76438891 | TGACGCCATGCACAC[C/T]GAGGGCACAGAGGAC | 63893 |
| rs566354468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439344 | TCTTCCACCCCACCT[C/T]TAGCTCAGTGGTCCT | 63893 |
| rs566444042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448194 | GAGGCCCGAGGGCTA[C/G]AAGGGGAAAAATCAA | 63893 |
| rs566449805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393650 | CAGTTCCAGGCTGGT[A/G]AGGCCTGGGGAAGGG | 63893 |
| rs566469042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76417276 | CCAGCCGAAAGTCAA[C/T]GACATCCCTGGGCAG | 63893 |
| rs566526370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411847 | CATGCCACCACCCGG[C/T]TAATTTTATTTTTTT | 63893 |
| rs566546000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76399367 | GGTGTGTGTGCGAGC[A/G]CAGGCACGCACACCG | 63893 |
| rs566589125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76412675 | ACTATAGTTCAAGAC[A/G]GGGGTCACGTGTGTT | 63893 |
| rs566601959 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76441477 | CCTTTGGACAATTCC[C/T]GGTTCATTAACACTG | 63893 |
| rs566622468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76448682 | CTTTGCCTCCGAAAC[A/G]AAGGCTGAACTTGAA | 63893 |
| rs566637739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406190 | TTGGAGCCCGGCCAA[C/T]TGCACGAGCACCTGA | 63893 |
| rs566683884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442809 | TCAGTTGGCGGCAGC[A/G]CTGTTCACTGGTTGA | 63893 |
| rs566692472 | snp | C/T | 6.94481e-05 | 0.0058923 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399907 | CACAACCTGCTTCTT[C/T]AACAGGCGCTTCACC | 63893 |
| rs566730666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76404023 | AAAGAATACATAAAT[A/G]GGGCAGAAGATAAAG | 63893 |
| rs566758741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436838 | CGAGGAGCATTTATT[C/T]CAACATTTAAAAGGC | 63893 |
| rs566788171 | snp | C/T | 0.000380294 | 0.0137841 | missense | UBE2O | GRCh38.p7 | 17:76397848 | CACACCACCTCCACC[C/T]TGCTGCTGACGTCCA | 63893 |
| rs566812092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76430213 | TGTTTTCTCTCCCAT[C/T]CTGTGTCCTTGTGGG | 63893 |
| rs566814704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403583 | GTGAACTCTGCCTGA[A/G]CTCATATATTTTAAT | 63893 |
| rs566847398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76424877 | TATTTTTTATTTTTT[A/T]TTTTTGAGACAGAGT | 63893 |
| rs566872264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76447380 | GCACCACAGGGTTGT[C/T]GTGAGCGTGAAGTAA | 63893 |
| rs566994695 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428498 | ATAGTAACTTTTTAT[A/T]TCATGGATAAAATAT | 63893 |
| rs567020726 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76422568 | GGTGTCCGAGCAGGA[C/T]GGAGGTTCCATCTGC | 63893 |
| rs567070190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432827 | CATGGCCAATAAGCA[A/C]ATGAAAAGATGCTCA | 63893 |
| rs567084686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447494 | AATACTCTATCATCT[C/T]TGTAATTTATAATCT | 63893 |
| rs567123440 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449689 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACCTGA | 63893 |
| rs567174649 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE2O | GRCh38.p7 | 17:76444758 | TGGGGGACCAGAGAA[A/G]TGCTTTCTTCCTTGG | 63893 |
| rs567183114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76401825 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCGTTGC | 63893 |
| rs567202358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76416616 | CACCAACCTCCCCGC[A/G]CTTCTCAAACACCTG | 63893 |
| rs567204511 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76397207 | GGGGAGCTGGGAACA[A/T]ATGACAAGAGGGGAC | 63893 |
| rs567215115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444312 | CCAACACTTTGGGAA[C/G]CTGAAGTGGGAGGAT | 63893 |
| rs567270979 | snp | A/G | 1.64773e-05 | 0.00287026 | missense | UBE2O | GRCh38.p7 | 17:76395783 | GAGGTAGCCAGCAGC[A/G]CCATCTCCTTCCGCA | 63893 |
| rs567283442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394350 | AGGTGGCAGGCAAAC[A/G]GGCTTGCCTGTTCCG | 63893 |
| rs567426465 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389486 | GGTTTAATGGTGTCA[C/T]CTTGTCTTGCTAATG | 63893 |
| rs567524053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420156 | AATCAACAGCCACAC[C/T]CTGAAAATGCACCGT | 63893 |
| rs567556273 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76423933 | TTGAGACGGAGTCTC[A/G]CTCTGTCACCCAGGC | 63893 |
| rs567574928 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBE2O | GRCh38.p7 | 17:76406761 | CTGGAGTGCAATGGC[A/G]CAGTCTCGGCTCGCT | 63893 |
| rs567576281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76414536 | CAGGGACAGCCCCCA[C/T]GCCCTCACCCCTGAC | 63893 |
| rs567637592 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76407301 | CCAGGAGGCTGGAGA[C/G]GCATGCTGGCGTGAC | 63893 |
| rs567748888 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433704 | GTGACAGAGCGAGAC[G/T]CCATCTCAGAAAAAA | 63893 |
| rs567749309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419238 | GCAGTGAGCCACGAT[C/T]GCACCACTGCACTCT | 63893 |
| rs567775281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418794 | CAGGATGGTCTTGAT[C/G]TCCTGACCTCGTGAT | 63893 |
| rs567777447 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399392 | ACACCGAGGGGACGC[A/G]CACTCTGCCTGGCTT | 63893 |
| rs567790148 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410010 | GCTGAACCAGAGATC[A/G]GGATGAGATGGGGAA | 63893 |
| rs567899804 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76411160 | GGGACTACAGGCGTA[C/T]GCCACCATGCTTGGC | 63893 |
| rs567907000 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422504 | CACTGGGTGGGCAGA[C/T]GCTGTGCCAGATGCC | 63893 |
| rs567908958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410401 | TGGTATCTAGTGGGC[A/T]GAGGCCAGAATGCTG | 63893 |
| rs567937999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450009 | GGCAGGAGGATTGTG[A/T]GAGACCAGGAATTCA | 63893 |
| rs567972248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411002 | TTGAAAATACAAAGA[C/T]GCTAAATAAAGAAGC | 63893 |
| rs568034054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421807 | AATGCCACGTGCTTC[C/G]CATTTCTCCCATCCT | 63893 |
| rs568072768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428199 | TCATTCCCAGTCTTT[C/T]GTATGTGACCCGTTT | 63893 |
| rs568081299 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416323 | GAGCTTGCTGGAAAC[A/G]CAGACTCTCAGGCCC | 63893 |
| rs568144436 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451567 | GTTGTCACAGACCCC[A/G]CTTTGTAGTTTGACA | 63893 |
| rs568154218 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394664 | ATAATGTAAAAGTAT[-/A]AAAAAAAGGTCATCC | 63893 |
| rs568171174 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419641 | CCAGATCCCAGCCTG[C/G]GCCAGTTTCCATGCT | 63893 |
| rs568228756 | snp | C/G | 0.000159987 | 0.00894248 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452980 | CAGGCGCTGCGAGCC[C/G]GCTTCTGGGCCGGAG | 63893 |
| rs568242248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416453 | GAGCTGCTTCTGGGA[A/C]AATTTGGGGGAAACA | 63893 |
| rs568274993 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397491 | AGGAAAGTCTCCATC[C/T]CCTTTTAGGAGGGAA | 63893 |
| rs568294528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447019 | GCTCCCTACCCATCA[C/T]CTCCCTCCCTCCTGC | 63893 |
| rs568354816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415638 | GGTGAAACCTGGTCT[C/G]TACTAAAAATACAAA | 63893 |
| rs568358314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447501 | TATCATCTTTGTAAT[G/T]TATAATCTCATTACC | 63893 |
| rs568521848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408776 | GCCCACTCTGGGAAA[A/G]CACCAGATTTGTGAA | 63893 |
| rs568545189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448742 | TCGCAGGGGGCTGTT[C/G]TGCCCAACCATGACA | 63893 |
| rs568559821 | snp | A/G | 6.59033e-05 | 0.00573997 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402610 | ACTCTACCTGGCGCC[A/G]TTGGATAGCTTCAGG | 63893 |
| rs568567523 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410359 | TCTGGAGACACTTTC[A/G]GTGGTCATAAAGGGT | 63893 |
| rs568583036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439935 | CACCCACTAATTCCA[C/T]TCATTCGCATGTGTG | 63893 |
| rs568600902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439421 | GTCAAAAATTTTCTA[C/T]AACAAGACCAAGACG | 63893 |
| rs568608342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449237 | AAACTACAAAAATAC[A/G]CCACACCCTATGAAA | 63893 |
| rs568650446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403336 | GTGCAATGGTGTGAT[A/C]TTGGCTTAATGCAAC | 63893 |
| rs568678775 | snp | A/G | 1.64977e-05 | 0.00287203 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391075 | GATGTCAGGGTAGCC[A/G]CTCTTCTCAGGTAAG | 63893 |
| rs568819732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76427338 | TAGAGGCTTTATTTG[A/G]TTCTTTAAAAAATAA | 63893 |
| rs568831320 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427219 | TGCAGAATTCTAACT[A/T]ACTTCTGCAGATCTG | 63893 |
| rs568948615 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76393742 | GACCACCGCTCCACA[A/G]ACATCTGGAATCTGT | 63893 |
| rs568983757 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455126 | GTGAGATTCCGTCTC[-/A]AAAAAAAAGTAACTC | 63893 |
| rs568993767 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE2O | GRCh38.p7 | 17:76406598 | CTGCTAGTAGAAGAA[C/T]GTGACTCACAAAAAA | 63893 |
| rs569052246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437563 | AAGTGTATGGTTTAG[A/G]TAACAGTATGTGGCT | 63893 |
| rs569059174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429626 | ATAAGCAAGGCTCTG[G/T]ACAGGTGAGGACCAC | 63893 |
| rs569101514 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76431514 | TGTCTCAAAAAAAAA[A/G]TCAACAAAACCCAGG | 63893 |
| rs569150944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76398683 | CCCTGACCTTCCCCC[A/G]TCTTGGAAGTGGTGA | 63893 |
| rs569155719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430808 | AGAAGCTGCAACATC[C/T]TTTGGCCCTTTGGGC | 63893 |
| rs569177870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423805 | TGATAGAGGTGGCCT[A/G]CGGCACAGTGTCCGC | 63893 |
| rs569186831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76406231 | ACGCACAGCTGGCAG[C/T]GGCCACTGCCTCCTG | 63893 |
| rs569187267 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76392732 | CCGAGACGGGTGGAT[C/G]ACTTAAGGTCAGGAG | 63893 |
| rs569222883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76424595 | AAAATTAATTTCTGG[C/T]TGAGTGAGGTGGCTC | 63893 |
| rs569225958 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404229 | TTCCCACAAAATACA[A/G]TCACTTAAAGGGGGT | 63893 |
| rs569233856 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76437225 | GGAGGCCAAGGCAGG[C/T]GGATCACGAGGTCAG | 63893 |
| rs569265734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76399046 | CCCCCTCCGCGGAAA[A/G]GGCAGAGAGTCTTTC | 63893 |
| rs569340257 | snp | C/T | 8.24015e-05 | 0.00641825 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396429 | AGTCGGAGAGGTGGG[C/T]GAGCCCGTCAGCAGC | 63893 |
| rs569353305 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76393179 | GGGAGGATCACTTGA[A/C]TCCAGGAGGCTGAGG | 63893 |
| rs569453584 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449772 | AAAAATACAAAAAAT[C/T]AGCCGGGCGTGATGG | 63893 |
| rs569458680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426315 | CAAAAGAACTTTTTT[C/T]TACTCTACTTGACGT | 63893 |
| rs569490091 | snp | C/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451723 | TTCCTGCTTAGAAAT[C/G]TTTTCTTGAAGGGGA | 63893 |
| rs569526163 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426810 | GCTTATTCAGATTTA[C/T]CTGCACTTCCCAACG | 63893 |
| rs569634311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433395 | AAATAGGCAAACCCA[C/G]AGAGACAGAACATGG | 63893 |
| rs569667394 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390290 | CCACCTCTCCTGGGC[A/G]TCACCCGGAACCTAG | 63893 |
| rs569699015 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393475 | CCTGACCTTGTGATC[C/T]GCCCACCTTGGCCTC | 63893 |
| rs569775028 | in-del | -/TT/TTT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424207 | CCACCGCGCCCGGCC[-/TT/TTT]TTTTTTTTTTTTTTT | 63893 |
| rs569849005 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439278 | ACCTTTGTTGTTATC[A/G]TTATTTACAGTCCTG | 63893 |
| rs569878581 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE2O | GRCh38.p7 | 17:76433655 | TTGAACCCAGGAGGT[A/G]GAGTGAGTATTGCGC | 63893 |
| rs569905016 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE2O | GRCh38.p7 | 17:76415798 | AACAGAGCAAGACTG[G/T]GTGTGTGTGTGTGTG | 63893 |
| rs569906189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76413251 | CATTCACCCCCATCC[C/T]ACAATGTTAATGCAG | 63893 |
| rs569912370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76407317 | GCATGCTGGCGTGAC[A/G]GTGCCACTTTTCTAA | 63893 |
| rs569928072 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451722 | ATTCCTGCTTAGAAA[G/T]GTTTTCTTGAAGGGG | 63893 |
| rs569963482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418829 | CCGCGTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 63893 |
| rs569980538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76401277 | CACACACGCCCCACA[C/T]GCCCTAAAACAAGTC | 63893 |
| rs570018214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401921 | TTTCTGCCTATACCC[A/G]AACTTTTAGACCCTC | 63893 |
| rs570045700 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76451025 | AACAAAGTTAACCAC[C/T]AAAGTCAAGACGGAC | 63893 |
| rs570108088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419515 | CTGATGCCCACCCTT[C/T]GGCACTCCCTGACAC | 63893 |
| rs570145600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414979 | TCCTTCCTCAAAAGT[A/G]TAAGTAGAAGGCAGA | 63893 |
| rs570168412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414577 | ATCTCACAACGCAGA[C/T]TCTCAGGCTGGGCAA | 63893 |
| rs570212250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407824 | TTCCCGTGGGGTCTC[A/C]AGACAACAGCAGCTC | 63893 |
| rs570219398 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450184 | ATGGTCTTTCCTTTA[A/C/T]GGCATACTATCACCT | 63893 |
| rs570307572 | snp | C/G | | | missense | UBE2O | GRCh38.p7 | 17:76400536 | CCATGTAACTTTCAA[C/G]TCTACAACCTGCACC | 63893 |
| rs570375790 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76398730 | CAGTCCCCTTCTGGA[A/C]CTCATTTTAGCTCTG | 63893 |
| rs570451120 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453529 | TCCCTTGGCGTCCTA[C/G]CCTAGCCCCCAGGCA | 63893 |
| rs570460606 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76436527 | TATTACACCTGGGAC[-/T]TTTCCCTCCTTGCTG | 63893 |
| rs570473052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422502 | ACCACTGGGTGGGCA[A/G]ACGCTGTGCCAGATG | 63893 |
| rs570534705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416508 | CCCCAGGAGAAGAGG[A/T]GCCCTGGAGGGGCTG | 63893 |
| rs570554255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405081 | CAGCTGGCTGCTGTG[C/T]TCCGCCTTCTGACCC | 63893 |
| rs570592689 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76440059 | CTGTGCTTCTCTTAC[C/T]TTCCGGCTGGGGACA | 63893 |
| rs570655374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440521 | TTTGAAGAGATGGGG[G/T]TTCATCATGTTGCCC | 63893 |
| rs570676248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441765 | ATCCATTTATTCATG[C/T]TCTCTTCACTTCCCC | 63893 |
| rs570700558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436153 | TCAGGAGGCTGAGGC[A/G]GGAGAATTGCTTGAA | 63893 |
| rs570738778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442084 | GTCAAGTGCTTTAGG[C/T]GGGGTTCTTACAGGG | 63893 |
| rs570753311 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453327 | CTAGGGGACGCTGAA[A/G]ATGCCGCGGGGGGCG | 63893 |
| rs570756057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76409247 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 63893 |
| rs570918422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403567 | GTGAGCCACTGCGCC[C/T]GTGAACTCTGCCTGA | 63893 |
| rs570925036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443568 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 63893 |
| rs570959270 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76397299 | AGCCATTCCCGCCCC[C/G]ACTCCTGCCCCCTGT | 63893 |
| rs570962041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434709 | TAAGCAATTCCGACA[C/T]GGCAAAGGTCAGGAG | 63893 |
| rs570964978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434204 | GGATCCCTTCCAGTC[C/T]TACCACTATAGACCT | 63893 |
| rs570979774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403908 | AAGGGGTTCCCACTG[C/G]CTAAATCTGGGACCA | 63893 |
| rs570986311 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76437597 | GTTAATATCTTTTTT[A/G]CGAGATGCAGTCTCA | 63893 |
| rs570988532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444135 | CTGAGGCAGGAGAAT[C/T]GCTAGAACCCAGAAG | 63893 |
| rs571023330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428291 | TCCATTTACCATTTT[C/T]GAAACTTATGACTGT | 63893 |
| rs571052212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438129 | CTTTTGGTAGGTGAC[C/T]ACATGTCTACATCCA | 63893 |
| rs571100829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445709 | GCAAATAACTTGGAG[C/T]AGATAAATCCAGAGA | 63893 |
| rs571185693 | in-del | -/C | 0.000367702 | 0.0135542 | intron-variant | UBE2O | GRCh38.p7 | 17:76397932 | GGCCCAGCTCAAGCT[-/C]CAGCTCCCCAGCCCC | 63893 |
| rs571199087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406673 | CAGAGAGTCCCATGG[A/G]AACTCATGAGCCCAA | 63893 |
| rs571246280 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438853 | GTCAGCACCTCTAGC[A/G]CTCCACGCCATGCAT | 63893 |
| rs571293647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430975 | GTGCTTCACTTCTTC[A/G]TGCATAAGTTTCCTC | 63893 |
| rs571335125 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76393593 | TGCTCCAACCCTTAT[C/T]CCCAACAAGGCAAGT | 63893 |
| rs571371908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423342 | CCTGATTGTGCCAAT[A/G]CACTCCAGCCTGGGT | 63893 |
| rs571455555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76395135 | CCTGCCTCGGCTTCC[C/T]GAAGTGCTGGGATTA | 63893 |
| rs571482405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425118 | CCTCGTGATCCACCC[A/G]TCTGGGCCTCCTGAA | 63893 |
| rs571498317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418127 | GCTGCCCCACACTGC[C/T]CTGGGACGCCCTGAA | 63893 |
| rs571530508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76426329 | TCTACTCTACTTGAC[A/G]TAGTTGGGCTGGATA | 63893 |
| rs571556457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76429661 | GATGGAGTAGAAAGC[C/T]GGCCACTGCTGTGAG | 63893 |
| rs571565657 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434531 | TCACATGAAGAAAAA[A/C]GGATTCCAAGCATGA | 63893 |
| rs571591493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419712 | AAAGAGCAGATCCCG[C/T]CAGCACGCATCCTTG | 63893 |
| rs571655665 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76404675 | CTGTCCTCATTTTTG[A/G]AAAACACACAAGAGG | 63893 |
| rs571681353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430074 | CACCAATTGCCTCCA[A/G]TTCCTGATGCTTTCT | 63893 |
| rs571686847 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76414497 | GGAAGGCAGGAGGAC[C/T]GGGGTTGCAGGGGAA | 63893 |
| rs571712594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76420407 | CTGGCTTCCTGCATC[A/G]TTTTGTTTTCCTAAT | 63893 |
| rs571767218 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430631 | ATCTGTCAAAGCAAT[A/T]CGCTTCTTATTGATT | 63893 |
| rs571769643 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407358 | ATTCTGTGCCTGTAA[A/C]CCTCTGTGCCCAAAT | 63893 |
| rs571783535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455104 | TGCACTCCAGCCTGG[C/G]CGACAGAGTGAGATT | 63893 |
| rs571837880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448791 | CCACCACGTCTAGCC[A/G]GTGCTCATGAAGGTT | 63893 |
| rs571838819 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76415842 | GTGCATACACATATA[A/T]GTATATACAAATATA | 63893 |
| rs571893532 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404995 | GCCTATGCTGGGGTT[A/G]GGGAAGGGCACGTCC | 63893 |
| rs571921579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413619 | CCGTGAGTGACTGCT[A/G]AGAAGCTGGAGAATC | 63893 |
| rs572039233 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76403114 | GTAAATACGTTAACA[A/C]ATCAAGGATATCGAG | 63893 |
| rs572108055 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76451040 | CAAAGTCAAGACGGA[C/T]GGGAACAACAACTGA | 63893 |
| rs572184912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445895 | GGCACTCTTGCTCAG[C/T]AAGAGCTGCAAATGT | 63893 |
| rs572196988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76402180 | ACACAGTGAGTACCA[A/G]AAAGTTGCGATTCTG | 63893 |
| rs572218178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394810 | CCACTCAAAGGATCT[C/G]TAATGTTCTAATTTT | 63893 |
| rs572256116 | snp | A/T | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389114 | TCCACCGCCAGGTGC[A/T]ATGACGTCGGCTCTC | 63893 |
| rs572294664 | snp | A/G | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390645 | CTCTGACCTGAGAAG[A/G]GGCAGCAAGGGAGCA | 63893 |
| rs572302619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395427 | TCGATCTCCTGACCT[C/T]GTGATCCACCCACCT | 63893 |
| rs572328133 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438323 | TTATTTAAAAATGGT[A/T]AAAATGGTAAATTTT | 63893 |
| rs572341588 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389109 | ACCTGTCCACCGCCA[A/G]GTGCTATGACGTCGG | 63893 |
| rs572364302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76415895 | TATATGTACATACAC[A/G]TATATACAAATATAT | 63893 |
| rs572368084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449737 | CAGCCTGGCCACCAC[A/G]GAGAAACCCCGTCTC | 63893 |
| rs572401154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407344 | CTAAATCAAAGAATA[C/T]TCTGTGCCTGTAACC | 63893 |
| rs572426862 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389688 | CGGTTCCAAATGCCA[C/T]GGTGTGTGGTCCGGC | 63893 |
| rs572445915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76419862 | GTGGCTCTACCCACG[C/T]GGAAACCTCAGAGTC | 63893 |
| rs572458839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76401332 | CAAACCCTGGGTCCG[C/T]AGAGGTCATCTGGCG | 63893 |
| rs572475646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76400849 | TGGTCACTATGACCA[C/G]AGCCTGGGTTCCCTT | 63893 |
| rs572614841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432243 | ACCATGTCTTAGACC[C/T]GTCAAACTGCTACGG | 63893 |
| rs572734075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393302 | ATGGAGTATAGCTCT[C/G]TCCCCAGGCTGGAGT | 63893 |
| rs572774061 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76425799 | ACAAATTATCGATCA[C/G]GTATCTTTGGGCTTT | 63893 |
| rs572832764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447627 | ACTTTAAATGTGCAT[C/T]ACTGAATTTCTCACA | 63893 |
| rs572848696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76417101 | GGGGTTGGGCAACAC[C/T]GAGCTGAATGAGCTC | 63893 |
| rs572849588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405108 | ACCCAGGAAGGCTGT[C/G]CTTGGCAAGAGCACG | 63893 |
| rs572861359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433783 | TGCCAGCACTTTGGG[A/G]GGCCAAGGTAGGAGG | 63893 |
| rs572866960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411188 | GGCTAATTTTTGTAA[C/T]TTTTTGTAGAGAAAG | 63893 |
| rs572916396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434239 | ATACATGGAAACCCA[A/G]CACACAGTCCTATCT | 63893 |
| rs573033461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76435922 | GATGCTGCTGACTAG[C/T]TGGGGATCCTGCAGA | 63893 |
| rs573037105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422882 | AGCAAGTGCCTGGAA[C/T]ACAGAAGGGTGCCTC | 63893 |
| rs573098523 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76429215 | AGCCCTCTACTATGT[C/T]TGCAACTTCCTATGC | 63893 |
| rs573138002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423451 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGTGG | 63893 |
| rs573151771 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395340 | GCGCCCGCATGGTGG[C/T]GGGAGAGTTTTTTGT | 63893 |
| rs573211688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426790 | GATCACTTTCAGAAG[C/T]GAATGCTTATTCAGA | 63893 |
| rs573231946 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425087 | CATGTTAGCCAGGAT[A/G]GTCTCGATCTCCTGA | 63893 |
| rs573263715 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437686 | AACCTCCTGAGTAGC[A/T]TGGATTACAGGCACG | 63893 |
| rs573269550 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390641 | CCGCCTCTGACCTGA[A/G]AAGGGGCAGCAAGGG | 63893 |
| rs573298339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421565 | AGATGGGGTTTCTCC[A/G]TGTTGGTCAGGCTGG | 63893 |
| rs573325602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76431113 | CTGCTGCTTCTCTTC[A/G]ACACCCTCCATGGTT | 63893 |
| rs573333107 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417830 | GCGTCCGCGAAGAGA[C/T]GTCTGGGTGAAGAGA | 63893 |
| rs573389433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422135 | ACGTGTGCTAAGTAA[C/G]CCCAAAATGCTAGTT | 63893 |
| rs573479010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416044 | GTATATATGTGTGTG[C/T]ACATATGTACATACA | 63893 |
| rs573544492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76409857 | CCCATTCTCCTGCAG[C/G]GGGGATGCAGACAGA | 63893 |
| rs573663681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76424861 | TTTCTTTTTTTTTTT[A/T]TATTTTTTATTTTTT | 63893 |
| rs573725036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76418932 | TTCAACCCAAACCCA[C/T]TGAATAAATTTCTGG | 63893 |
| rs573762747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419750 | GGTGGACATGGTTTC[A/G]CCACCTTGAAGACTT | 63893 |
| rs573889606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406300 | CACCAGGCCAGCCTG[C/T]GTCTTTTTTAGCTGG | 63893 |
| rs573952653 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76414709 | TGAGTCCAACTGCCT[A/G]CTAAGTGAGGGGGAA | 63893 |
| rs573986861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76417761 | TATTGCAGGCCCAGG[C/T]GAGACAGGAGGAAGG | 63893 |
| rs573993508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76437266 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 63893 |
| rs574016417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407565 | TGGGGGTCCCTGAGA[C/G]AGCAGCCAGGAAAGG | 63893 |
| rs574016939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418258 | GAGCCCACAGCCTCC[C/T]GGAGGGCTCTCCAGG | 63893 |
| rs574059849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448451 | GAAATGCTGGCCAGC[A/G]TAGGAGCCAAAAATA | 63893 |
| rs574195897 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438274 | TGGGGATGGTTGCAC[A/C]ACAATGGGAATGTAC | 63893 |
| rs574211744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443002 | TAAAAATGACCCCAA[A/G]TGCTCTAATTTTGAG | 63893 |
| rs574226501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76409623 | CTGGTCTCCAACTCC[C/T]GACCCCATGACCTGC | 63893 |
| rs574248052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443692 | GGCACAATGGAGCTA[C/T]CAAGTAAGCAGCTGG | 63893 |
| rs574258238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76400611 | GCACTCTCTTTAGCC[A/G]GCTGCCCAAAGCCCA | 63893 |
| rs574443544 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76451124 | AGGAGGCCACAACAC[-/A]AGAGGATGCTGCAGT | 63893 |
| rs574481596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445957 | CAGGACTGGCACCCA[C/T]TCATGGGCAAGTGGA | 63893 |
| rs574495109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76446217 | GGGTGAAAACCCACA[C/T]GTCACAGAAAACCAC | 63893 |
| rs574529816 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448979 | AGCATATAAGAGACA[C/T]TGGCCACTAGCTCCT | 63893 |
| rs574570736 | in-del | -/GT | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76425237 | GACAAAAAAAAAAAA[-/GT]AAAAAAAAAAAAAGT | 63893 |
| rs574572326 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440386 | TTAAGGGCAATGGGT[C/T]GCACGATCACGGCCC | 63893 |
| rs574626024 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447932 | CCATCCTAGGCTTGA[C/T]CCAGCTACACTTCTG | 63893 |
| rs574632752 | snp | A/C/G | 4.94493e-05 | 0.00497219 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396261 | AGGTGACTGCCCCTC[A/C/G]GGCTTGTCCTCCTTG | 63893 |
| rs574720232 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76416147 | CGTGTATAGATATAT[-/AA]AGTGTGGCTTTATAT | 63893 |
| rs574724998 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390399 | GGAGTCAGTGACAGC[A/C]GCTACAACTCCCAAG | 63893 |
| rs574747094 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76444584 | AGCAAATGCAGTGAT[C/G]AGAAATTCACTAGTC | 63893 |
| rs574775111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76444962 | CCACACACACAGTCC[A/G]GTGACCACACACACA | 63893 |
| rs574809624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76438606 | TCACTACTCTAATAA[C/T]TGAAAGCTTTATTAC | 63893 |
| rs574833003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438908 | AGGGCACAGAGGACA[C/G]AACTCATCTGCCCCA | 63893 |
| rs574844431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76395492 | CCACTGCGCCCGGCC[A/G]AGAAAGTAATTTTTT | 63893 |
| rs574876637 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431779 | TCTCTATGAAAAAGT[-/A]AAAATTAAGAATAAA | 63893 |
| rs574879765 | snp | C/T | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76407940 | GGAGCAGAGTGGGAG[C/T]GACAAGGGGCTGGGG | 63893 |
| rs575044446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433097 | GGGTATAATATCCAA[A/G]AGAATTGAAAATATA | 63893 |
| rs575064059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76420469 | GAAATGTTACAGACT[C/T]GCCCACATCTTTACC | 63893 |
| rs575073893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421139 | AGTACTGCAGACTTC[C/G]CTCCAAAAGGCCGTT | 63893 |
| rs575104494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76425997 | TTCACAGGAGGCACT[C/T]TTTTTCCAGCCCTTA | 63893 |
| rs575105261 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76442888 | CATGAGGCAAGCAGA[C/G]AGCAAACCAGGGTTG | 63893 |
| rs575109419 | snp | A/G | 4.94719e-05 | 0.00497328 | missense | UBE2O | GRCh38.p7 | 17:76398932 | ATGTTGCATTCCACG[A/G]AGCCATCCTGCCACA | 63893 |
| rs575110314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433604 | TGAATTGTCTCAATA[A/T]ACCTTTTTTTTTTTA | 63893 |
| rs575172545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426506 | TTTTCTTTGCTCTCT[G/T]TCTTTTAGACAAATG | 63893 |
| rs575195350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76427961 | TCCAATGAACCCACC[C/T]TGCCCCTCCCCAGAG | 63893 |
| rs575216033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76392975 | AAAGATTGTATTCCT[C/T]AGCCAGACGTGATGG | 63893 |
| rs575255663 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76428569 | CTTTCTCCTACCTGA[A/C/T]TCAGCTCTGATTCCT | 63893 |
| rs575285728 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76416070 | ATACACGTATATACG[-/TA]TGTGTATACATATGT | 63893 |
| rs575356536 | snp | A/C | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452621 | CCGCGTCGGCCACTG[A/C]AGTGGCACCGCTCCG | 63893 |
| rs575403063 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453249 | ATAGCGCGCTGACGT[A/G]TCCCTGCGTGGCGCC | 63893 |
| rs575515370 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394364 | CGGGCTTGCCTGTTC[C/T]GGAAGGATGCACTCA | 63893 |
| rs575525145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447770 | GAAACAACCACCTTC[A/C]CCACAACCCGCCTCG | 63893 |
| rs575530751 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76430242 | GGTTTATACATCTAA[A/G]AACAATTATTTTGCT | 63893 |
| rs575532583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76423460 | GCACTTCGGGAGGCC[A/G]AGGTGGGAGGATCAT | 63893 |
| rs575550580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76435137 | GAGTCACCACGAAGC[A/G]AACGGGAAGGTCAGG | 63893 |
| rs575596026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76424031 | TCCTGCCTCAGCCTC[A/C]TGAGTAGCTGGGACT | 63893 |
| rs575635766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425281 | GTGGTCACTAAAAAA[A/T]TTTAAAGGACCTACT | 63893 |
| rs575697496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76419801 | GTGGCCCTGAGAACC[C/T]GATGCTCAGAGCTGT | 63893 |
| rs575721997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401498 | GTGTGTCCATGTACT[A/G]TTGTAACTAACACAT | 63893 |
| rs575780232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420293 | ATCCAAGGCCAGTTG[C/T]TTCCCCGGGGGCCAA | 63893 |
| rs575803851 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401512 | TATTGTAACTAACAC[A/G]TCATCCTGTACTGAG | 63893 |
| rs575806419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416754 | GCTGGGTCATTAGGT[C/T]CTAAGACCCTCAACT | 63893 |
| rs575866718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76450942 | TCGATTTAACTCCAA[A/C]ATAGGTATTTCAAGT | 63893 |
| rs575867698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411366 | GCGGATGGCTCCTAA[A/C]GGCTGGGCTGCTCCT | 63893 |
| rs576042086 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76405151 | GCCCAGAGGTCGTGC[C/T]GCCGAGAGAACCAGA | 63893 |
| rs576135579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414729 | GTGAGGGGGAAGGAC[C/T]GCAGAGCTTGGCCTG | 63893 |
| rs576164433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76406846 | GTGGGACTGCAGGCA[C/T]GTGCCACCACGCCCG | 63893 |
| rs576167332 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76404041 | GCAGAAGATAAAGCT[C/T]TTCTACAGAGCAGAA | 63893 |
| rs576283685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76418897 | AGGCAGTTGTTTATC[A/G]GCTTGAAAAACACGG | 63893 |
| rs576359418 | in-del | -/AAACTT | 0.00874735 | 0.0655527 | intron-variant | UBE2O | GRCh38.p7 | 17:76438371 | ACAATTAAAAAAGAA[-/AAACTT]AAAGGCTCCTCGTCG | 63893 |
| rs576368247 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76424869 | TTTTTTTTTATTTTT[A/T]ATTTTTTTTTTTTGA | 63893 |
| rs576442844 | snp | A/G | 5.0491e-05 | 0.00502424 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402103 | GTCGTAGAGCTTGGC[A/G]CCATCTTCCGTGTTC | 63893 |
| rs576481344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403757 | AAACAATGAGGCTTC[C/T]TGGAGAAATGGTTGA | 63893 |
| rs576511960 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76435515 | AGCTAATTCGCAATA[A/T]TCCCCCCGTTTACTG | 63893 |
| rs576542663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76397582 | GTCTACATGCACCCA[A/G]AGATGGACGTGAAGA | 63893 |
| rs576593412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76437755 | CGACAAATATATATC[A/G]TGATATGTAAGATGT | 63893 |
| rs576604137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449696 | GGCCGAGGCGGGCGG[A/C]TCACCTGAGGTCAGG | 63893 |
| rs576604265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76443142 | CAGATAAGGCAAATA[C/T]GGCAGGATGTTAACA | 63893 |
| rs576641485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438343 | TGGTAAATTTTGTTA[C/T]GCATATTTTACTACA | 63893 |
| rs576651882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76431217 | GATGAAGGAGAAGTA[A/G]TAAGTCAACAAAAGC | 63893 |
| rs576666026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443741 | GAAGTCACCTAAATA[C/T]AGGTACCAGATGCAG | 63893 |
| rs576706149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432145 | AGAATCTGTGAGGCA[C/G]CAGCAGCCAAGAGCC | 63893 |
| rs576736891 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452401 | GTAACGCCGAACGCG[C/T]CCCAGAACCTGAGTC | 63893 |
| rs576752674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76409722 | TTGCACACATGTGAC[A/T]CAACAGTGGGGCTGC | 63893 |
| rs576765590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422278 | CTAAATGAACAACAC[A/G]GGGAGAGGGCATGGG | 63893 |
| rs576962157 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416806 | TCTCCCAAGGCACAA[C/G]AGCAACAAGCAGCTC | 63893 |
| rs577003095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440370 | GCTCTGTTGCCTAGG[C/T]TTAAGGGCAATGGGT | 63893 |
| rs577027726 | snp | A/C | 2.0609e-05 | 0.00321 | missense | UBE2O | GRCh38.p7 | 17:76392028 | GGCACGGCTGGGTAG[A/C]TGTTGGGGAGCTGGA | 63893 |
| rs577047284 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2O | GRCh38.p7 | 17:76435841 | GCTCAGTGACACCCC[A/G]GCACAGAGGGGACAG | 63893 |
| rs577067105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440968 | CCCAGCACAGTGCAG[A/G]GGGCACCCGTGTAGT | 63893 |
| rs577083283 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76419553 | CTGTGGTCCAGCCCT[C/T]GGGAAAGACACAGAG | 63893 |
| rs577111089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429147 | CCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 63893 |
| rs577119255 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76436198 | GTTACAGTGAGCCGA[G/T]ATAGCACCATTGCAC | 63893 |
| rs577184091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439513 | ATGATGTGTGATGAC[A/G]TCACTGCTCTGATGG | 63893 |
| rs577231788 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | UBE2O | GRCh38.p7 | 17:76437135 | GCCTGGGCAACAAAG[G/T]GAGACTCCATCTTTA | 63893 |
| rs577233009 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389881 | TTACATACATACACC[A/C]AAAATTACATAGCTG | 63893 |
| rs577247509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433728 | GAAAAAAAAAAAAGA[A/G]AGAGAGAGATGGGGT | 63893 |
| rs577339762 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441201 | GGAATCCATTGACAC[C/T]GGCTGGATAAAAGAC | 63893 |
| rs577372830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76427585 | TTCCAAAAGGCCTGT[A/G]CTGTGCAAGGGTCAC | 63893 |
| rs577380856 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443351 | TGGAGTGCCGGGGCA[C/T]GATCTCGGCTCACTG | 63893 |
| rs577432135 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE2O | GRCh38.p7 | 17:76415914 | ATACAAATATATACA[C/T]ATGCACATACACGTA | 63893 |
| rs577442288 | in-del | -/AT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446216 | TGGGTGAAAACCCAC[-/AT]GTCACAGAAAACCAC | 63893 |
| rs577456412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426697 | AAGAACTTAAGAGTG[C/T]GTTCATTCAAATCAC | 63893 |
| rs577495115 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76416028 | ACATATGTACACACA[C/T]GTATATATGTGTGTG | 63893 |
| rs577577644 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76421487 | TGTCCTGCCTCAGCC[G/T]CACAAGTAGCTGGGA | 63893 |
| rs577578712 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76429917 | CTCTGCTCTCTCACT[C/T]GCCAGCAAAGGGGAT | 63893 |
| rs577671117 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76409399 | AAAATGAACACACAC[-/T]ACTTTTTTTTTTTTT | 63893 |
| rs577678002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416986 | GGAGTATAAGCTTCA[A/G]GGCACAGGGACCAGG | 63893 |
| rs577711435 | snp | C/T | 6.63867e-05 | 0.00576099 | missense, intron-variant | UBE2O | GRCh38.p7 | 17:76400158 | ATACCTTCTTGGCCA[C/T]AGAGCCCTCCCCCTG | 63893 |
| rs577740955 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76417528 | ACCTCCTTGTTAATA[C/T]GGTCAAAATTCTCTA | 63893 |
| rs577749393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393825 | GACAGGGCAATGGGC[A/G]AGGTCAGTGATGAGC | 63893 |
| rs577762531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76424734 | AATGGCAGCAGGATC[A/C]CTTAAGCCAGGTGTT | 63893 |
| rs577916972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76418388 | AGGAGCCATGCCTTA[C/T]AACCAGCAACTGCGA | 63893 |
| rs577974262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413369 | CATATTCCCCAAAGC[A/G]GCACTTTTTTTCAAA | 63893 |
| rs578042341 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453917 | GACCACGGATTCCAA[C/T]TTTTGGCACTGCCAC | 63893 |
| rs578047966 | in-del | -/GT | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76393790 | TCTGTGCACACACGC[-/GT]GTGTGTGGGATCTCA | 63893 |
| rs578049204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76401522 | AACACATCATCCTGT[A/G]CTGAGAGAGACAAAG | 63893 |
| rs578073716 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453846 | GATAAATTCAAAGCT[C/T]CCTGAAGCCAAGAAT | 63893 |
| rs578083738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447844 | CCTCTTTCTCATGGA[A/C]GTGATCTTCTGAAGG | 63893 |
| rs578102907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454706 | TGTGCACCTGTAGTC[C/T]CAGCTACTTGGGAGG | 63893 |
| rs578114827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76412099 | TCAAGGACAAGCGGA[C/T]GACCAGCCCCACACT | 63893 |
| rs578144105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448340 | ACTTCTTCACATTAC[A/G]TCACTAAGAACAATT | 63893 |
| rs578159973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76405731 | ACCGCACACACCTCC[A/G]ACCAGCACCCAGACC | 63893 |
| rs578206791 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401854 | GCACTCCAGCCTGGG[C/T]GACAGTGAGACTCTG | 63893 |
| rs578252986 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395462 | CTCCCAAAGTGCTGG[G/T]ATTACGGGTGTGAGC | 63893 |
| rs745362727 | in-del | -/ACA | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389509 | TGCTAATGAGCCAAC[-/ACA]AAAAAAAAAAAAAAA | 63893 |
| rs745366704 | in-del | -/A | 1.81817e-05 | 0.00301504 | intron-variant | UBE2O | GRCh38.p7 | 17:76402179 | GACACAGTGAGTACC[-/A]AAAAGTTGCGATTCT | 63893 |
| rs745380256 | snp | C/T | 1.75523e-05 | 0.00296241 | intron-variant | UBE2O | GRCh38.p7 | 17:76398626 | CTAGCTAAGGGATCC[C/T]GGCTAAGGAGCCCAC | 63893 |
| rs745385708 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413497 | GTAAGAATAAGTACT[A/G]TTAGGTTGGCAAAAA | 63893 |
| rs745447812 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430367 | TTCAATTTGAGAGCA[A/G]GTACTATTTATTAAC | 63893 |
| rs745481207 | snp | C/T | 1.74014e-05 | 0.00294965 | intron-variant | UBE2O | GRCh38.p7 | 17:76401191 | GAAAGTCCCCGTGAG[C/T]GGTGTCTCCATGGGT | 63893 |
| rs745491281 | in-del | -/TATGTGTGTG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416199 | ATATGTATATGTGTA[-/TATGTGTGTG]TATATGTATGTATAT | 63893 |
| rs745498481 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401594 | AAATAAAAGTTCTAA[A/T]ACTGCCGGGCGCGGT | 63893 |
| rs745552878 | snp | A/G | 3.29968e-05 | 0.00406169 | missense | UBE2O | GRCh38.p7 | 17:76391511 | ACCACGCGGATCAGC[A/G]CCATCTCATTGTAAC | 63893 |
| rs745568315 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444668 | AAAATGACTGAAGGC[A/G]AGAGCAGGTCATGAG | 63893 |
| rs745639003 | snp | C/T | 1.65422e-05 | 0.0028759 | intron-variant | UBE2O | GRCh38.p7 | 17:76397759 | CGGCCCAAGTTGCCA[C/T]AGTCACAAGCTCAGC | 63893 |
| rs745641474 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445882 | GCAATTCCGAACGGG[A/C]ACTCTTGCTCAGTAA | 63893 |
| rs745714423 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76406035 | AGGACACTGGGCTGC[A/G]GTGGGTCACCCTGAA | 63893 |
| rs745726745 | snp | A/T | 1.69599e-05 | 0.00291199 | intron-variant | UBE2O | GRCh38.p7 | 17:76395689 | ACTGGGTGCCCACAC[A/T]GCACATCTGCACCTG | 63893 |
| rs745754238 | snp | A/G | 1.69235e-05 | 0.00290886 | missense | UBE2O | GRCh38.p7 | 17:76405307 | CGATCACCGTGCCAC[A/G]CTGACTGTCCTGGGG | 63893 |
| rs745772869 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394800 | TCTTCCATTTCCACT[A/C]AAAGGATCTGTAATG | 63893 |
| rs745799502 | in-del | -/ACAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447555 | TTTCAGACTCTGGAA[-/ACAT]ACATACATACATACA | 63893 |
| rs745815844 | in-del | -/GG | | | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453412 | GGAGCGAGAAGGGGC[-/GG]GGGGACCCGGGAGGA | 63893 |
| rs745825932 | snp | C/T | 1.80876e-05 | 0.00300724 | missense | UBE2O | GRCh38.p7 | 17:76390947 | GTGCCTGGCAGCTAC[C/T]TGTCCTCTGTGCACT | 63893 |
| rs745832941 | snp | C/T | 1.648e-05 | 0.0028705 | missense | UBE2O | GRCh38.p7 | 17:76398514 | CTTGAACCACTTCAC[C/T]ATGCAGGTACGGCCG | 63893 |
| rs745858375 | snp | C/T | 3.30721e-05 | 0.00406632 | missense | UBE2O | GRCh38.p7 | 17:76400262 | CGCTCCCCAAGCTGC[C/T]GCTGAGCATGGTCAA | 63893 |
| rs745860384 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438435 | CACTAATGTCCCTAC[C/T]CCTGCTCTGTCTCCC | 63893 |
| rs745886029 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397784 | CTCAGCAGGGGGGTC[G/T]TGCCAGAGCCTCACC | 63893 |
| rs745896489 | in-del | -/AG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438216 | TTATTTAATTGAGAC[-/AG]AGTTTCAGTGGGGAA | 63893 |
| rs745912636 | snp | A/G | 3.05274e-05 | 0.00390676 | intron-variant | UBE2O | GRCh38.p7 | 17:76396036 | GCTGGGGTCTGGCGA[A/G]GGGACTAACCACCCT | 63893 |
| rs745943321 | snp | A/G | 1.76537e-05 | 0.00297095 | intron-variant | UBE2O | GRCh38.p7 | 17:76400413 | CCCACGCGTGCCCCT[A/G]GGTTGCTGGCAGTAA | 63893 |
| rs745952082 | snp | C/T | 1.78912e-05 | 0.00299086 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452744 | GTCTCCTTCACATGC[C/T]GCTTGACGCCCTCCG | 63893 |
| rs745986422 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441243 | TAAAATGCTGAATAA[C/T]CATTCTCCTCTTGGA | 63893 |
| rs745998318 | snp | A/G | 3.30666e-05 | 0.00406598 | missense | UBE2O | GRCh38.p7 | 17:76391154 | ACCGATGCGTCTGGT[A/G]CGGTCTCCGAAGTCT | 63893 |
| rs746054159 | snp | C/T | 1.75203e-05 | 0.00295971 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400524 | ACTCTTGGTAATCCA[C/T]GTAACTTTCAACTCT | 63893 |
| rs746061392 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430328 | CCATGTTTACCTAAA[A/G]TATGCTAACCGAAGA | 63893 |
| rs746111143 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426276 | AAAGTGCTGGGATTA[C/T]AGGCGTGAACCACCA | 63893 |
| rs746117748 | in-del | -/ATACACACACACACAC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435400 | TGTTTAAATATACAG[-/ATACACACACACACAC]ATACACACACACACA | 63893 |
| rs746126113 | snp | G/T | 3.3379e-05 | 0.00408514 | missense | UBE2O | GRCh38.p7 | 17:76391285 | TTCTTGTTGGCCGGA[G/T]TCTGACAGCTCGGCT | 63893 |
| rs746126675 | in-del | -/TT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423896 | TTCCAGGTTGGGTTC[-/TT]TTTTTTTTTTTTTTT | 63893 |
| rs746176496 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420497 | ACCCAAACACACCAC[C/T]GAGCAACCCTACATG | 63893 |
| rs746202436 | snp | C/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390061 | CTGACAGTAGGCCTT[C/T]TAGTCCAAGAGAGGG | 63893 |
| rs746212527 | snp | C/T | 3.39593e-05 | 0.0041205 | intron-variant | UBE2O | GRCh38.p7 | 17:76391634 | TGGGCGGGACACCTT[C/T]CCTCAGTGGGTGAGA | 63893 |
| rs746231855 | snp | C/G | 1.6477e-05 | 0.00287024 | missense | UBE2O | GRCh38.p7 | 17:76399687 | TGCCTTCTTTTAGCA[C/G]GAATGGGGGCAGCTG | 63893 |
| rs746251977 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434294 | CTGCAATAAGCACAC[A/G]GTGGCTGAAAACTCC | 63893 |
| rs746290342 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439800 | CTTATCTTTCAAGAG[G/T]GAACTCAAAAGGCAC | 63893 |
| rs746317437 | snp | G/T | 3.31115e-05 | 0.00406874 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76397868 | GCTGACGTCCACACG[G/T]GCCACCTGGCCCACC | 63893 |
| rs746319735 | snp | A/C | 1.64787e-05 | 0.00287038 | missense | UBE2O | GRCh38.p7 | 17:76399764 | ACTGGACTGGCAGAG[A/C]CATCGGGCGTCTCCT | 63893 |
| rs746403346 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440954 | CTCTCCCCACAGCAC[C/T]CAGCACAGTGCAGGG | 63893 |
| rs746407523 | snp | A/G | 1.65201e-05 | 0.00287398 | intron-variant | UBE2O | GRCh38.p7 | 17:76398215 | CAGCTGGTGCACAGG[A/G]CAGTGAGCAGCCATC | 63893 |
| rs746416460 | snp | C/G | 1.65803e-05 | 0.00287922 | intron-variant | UBE2O | GRCh38.p7 | 17:76395900 | AGTCCCTCATGGAGA[C/G]GCCCTGGAGCTCCAT | 63893 |
| rs746429059 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450706 | AGCTCACCGCAACCT[C/T]CGCCTCCCTGGTTCA | 63893 |
| rs746435300 | snp | C/G | 0.000164401 | 0.00906495 | missense | UBE2O | GRCh38.p7 | 17:76405522 | ACTCACGGTGGATCG[C/G]ATGTGCCGGACCACA | 63893 |
| rs746487000 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454683 | CAAAAATTAGCTGGG[C/T]GTGGTGGTGTGCACC | 63893 |
| rs746506572 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410293 | GAGGCTGGTTAGCCC[A/G]GTGGTTCTCACCTAG | 63893 |
| rs746518566 | snp | A/G | 4.96857e-05 | 0.00498401 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396522 | GCTCTTGGGTGGCCC[A/G]TCCTTGCCAGCCTTC | 63893 |
| rs746540983 | snp | C/T | 8.40852e-05 | 0.00648348 | missense | UBE2O | GRCh38.p7 | 17:76402090 | CGTGCGGGCAGACGT[C/T]GTAGAGCTTGGCGCC | 63893 |
| rs746557953 | in-del | -/CAAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444235 | ACAAACAAAGCAAAA[-/CAAAA]CAAAACAAAACAAAA | 63893 |
| rs746598645 | snp | A/C | 1.70662e-05 | 0.00292109 | intron-variant | UBE2O | GRCh38.p7 | 17:76391657 | GGGTGAGAGAGGCCC[A/C]CAATGCAGGCCTACC | 63893 |
| rs746600674 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434994 | GGCAGAGCTGGGCTC[C/T]CCCTGCAGTGGCACA | 63893 |
| rs746600991 | snp | C/T | 6.5937e-05 | 0.00574144 | intron-variant | UBE2O | GRCh38.p7 | 17:76402574 | CTATCCTTCCCAAGC[C/T]GATGGCTCTCTGGTG | 63893 |
| rs746621547 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399195 | ACAGGATCCACTTGG[C/G]AGAGCTCAGGCAAAT | 63893 |
| rs746649174 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413320 | GTTTATCCCAGTGTG[G/T]ATTTCTGAAAAAGCT | 63893 |
| rs746688712 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433549 | GTATACTAAAAACCA[A/C]TTGAACTGCACACTT | 63893 |
| rs746688855 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399769 | ACTGGCAGAGCCATC[A/G]GGCGTCTCCTCAGGG | 63893 |
| rs746800237 | snp | C/T | 3.5536e-05 | 0.00421506 | missense | UBE2O | GRCh38.p7 | 17:76390959 | TACTTGTCCTCTGTG[C/T]ACTCCGGCATGCCTG | 63893 |
| rs746802125 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416171 | CTTTATATACACATA[C/T]GTGTGTGTGTGTATA | 63893 |
| rs746802263 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403564 | GGGGTGAGCCACTGC[A/G]CCCGTGAACTCTGCC | 63893 |
| rs746803974 | snp | A/G | 1.6615e-05 | 0.00288223 | missense | UBE2O | GRCh38.p7 | 17:76400295 | CATCCGAGACGCTTC[A/G]CCCTGGTTGGGGAAG | 63893 |
| rs746807610 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446937 | AATGACTGAGGGGTC[A/C]GGGAATGAAAAGAGT | 63893 |
| rs746848324 | snp | A/G | 0.000116558 | 0.00763317 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391054 | AAGTGGGAAGAGGGG[A/G]AAGCCGATGTCAGGG | 63893 |
| rs746874943 | snp | A/G | 1.69533e-05 | 0.00291142 | intron-variant | UBE2O | GRCh38.p7 | 17:76398786 | ACAAGCCCCAACCCG[A/G]GCCCTCATTGGCGAC | 63893 |
| rs746931536 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392990 | CAGCCAGACGTGATG[G/T]CTCACACCTGTAATC | 63893 |
| rs746940120 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76437331 | GGCGGGCACCTGTAG[G/T]CCCAGCTACTCAGGA | 63893 |
| rs746960916 | snp | C/T | 3.29511e-05 | 0.00405887 | missense | UBE2O | GRCh38.p7 | 17:76396400 | TTCTCCCGAGTTGGC[C/T]TCTCAGGCTCCACAG | 63893 |
| rs747009607 | snp | A/T | 1.64833e-05 | 0.00287078 | missense | UBE2O | GRCh38.p7 | 17:76398878 | GGGCAGAACTCGTTG[A/T]TGTCCAGGTGGTGCA | 63893 |
| rs747013689 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447959 | TCTGGTTATTCCATC[C/T]GAGCAGGATCATATC | 63893 |
| rs747058420 | in-del | -/CC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428807 | TGCACATATTGTGTA[-/CC]CATGTCAATTCCCTG | 63893 |
| rs747122028 | in-del | -/ACACAC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435418 | CACACACACACACAT[-/ACACAC]ACACACACACACACA | 63893 |
| rs747128445 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441255 | TAATCATTCTCCTCT[C/T]GGATTGGGTGTGTTA | 63893 |
| rs747181080 | snp | A/G | 1.67626e-05 | 0.002895 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391386 | GGGCATGGGTTTCCA[A/G]CCAGGACTCGATACG | 63893 |
| rs747186133 | snp | A/G | 1.71531e-05 | 0.00292852 | intron-variant | UBE2O | GRCh38.p7 | 17:76399417 | TGGCTTCACGCTGAC[A/G]CCATTGGGGAGGGGC | 63893 |
| rs747199265 | snp | C/G | 3.7527e-05 | 0.00433152 | intron-variant | UBE2O | GRCh38.p7 | 17:76396870 | ACAGGAAGTCACCTC[C/G]CCACCACTAAGGAGG | 63893 |
| rs747386430 | snp | C/T | | | missense | UBE2O | GRCh38.p7 | 17:76398266 | GTACCTCATCCTCCT[C/T]GTGAGGAGCCCCATC | 63893 |
| rs747393750 | snp | C/T | 1.67618e-05 | 0.00289493 | missense | UBE2O | GRCh38.p7 | 17:76399867 | CCCGGGAACACTGGG[C/T]GTCTGGGGAGCATGA | 63893 |
| rs747414784 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449567 | GTGACAGAGAGAGAC[C/T]CTGTTTAAAAAAGAA | 63893 |
| rs747445568 | in-del | -/GCAC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435105 | ACTAAGGGATGAGAT[-/GCAC]GCACCAAGCCAGCTG | 63893 |
| rs747459850 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419516 | TGATGCCCACCCTTC[A/G]GCACTCCCTGACACA | 63893 |
| rs747460273 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393368 | CTCCCAGGTTCAAGC[A/G]ATTCTCTGCTTCAGT | 63893 |
| rs747462062 | snp | C/G | 2.98245e-05 | 0.00386152 | intron-variant | UBE2O | GRCh38.p7 | 17:76396050 | AGGGGACTAACCACC[C/G]TGCACCCAGATCTGG | 63893 |
| rs747462248 | snp | A/G | 6.58957e-05 | 0.00573964 | missense | UBE2O | GRCh38.p7 | 17:76398299 | CAGTATTGCCGATGC[A/G]GATGACGATGTCAGT | 63893 |
| rs747471107 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400052 | CATCAGGGCTGCCCC[C/G]CAAGGCCTAAAGCAC | 63893 |
| rs747526884 | snp | A/G | 0.000305904 | 0.0123636 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452899 | GTCCTCGCCGTGGAT[A/G]AGGCGCACCAGCCCG | 63893 |
| rs747548323 | snp | A/G | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389165 | AACTGGTCAGTTGTA[A/G]GTCTCTGGAGACTAC | 63893 |
| rs747550257 | snp | C/T | 1.75545e-05 | 0.00296259 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396138 | CTCACAGGGTGCAAA[C/T]TCCAGTACGGAGAAG | 63893 |
| rs747555562 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392884 | CTTCAACCCGGAGGC[A/G]GAGGTTGCAGTGAGC | 63893 |
| rs747563919 | in-del | -/TT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403498 | GCTGGTCTTAAACTC[-/TT]GAGCTCAAGTGATCC | 63893 |
| rs747565244 | snp | C/T | 1.94237e-05 | 0.00311632 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400548 | CAACTCTACAACCTG[C/T]ACCTGGGGATGGCAG | 63893 |
| rs747581177 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418632 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 63893 |
| rs747590420 | in-del | -/ACAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435414 | GATACACACACACAC[-/ACAT]ACACACACACACACA | 63893 |
| rs747631780 | in-del | -/AC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447246 | TATTCTCAGGTGAGA[-/AC]AAAGTACATTTAGTT | 63893 |
| rs747659265 | snp | G/T | 1.64806e-05 | 0.00287054 | missense | UBE2O | GRCh38.p7 | 17:76399783 | CGGGCGTCTCCTCAG[G/T]GCTGGCAGACTCCGC | 63893 |
| rs747671147 | snp | C/T | 1.65822e-05 | 0.00287938 | intron-variant | UBE2O | GRCh38.p7 | 17:76391841 | GGGCACCATCAATTC[C/T]GTTCCCCAGGCCCCT | 63893 |
| rs747678904 | snp | A/G | 1.76524e-05 | 0.00297084 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391952 | GACACACACCTTCCC[A/G]TTGTCATACAGGTTG | 63893 |
| rs747681036 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404655 | TATGGTGGTTGCACA[A/G]GAGGCTGTCCTCATT | 63893 |
| rs747732499 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413544 | TATTTTGAAAAAACC[C/T]GTTCAGTTGCATATA | 63893 |
| rs747746753 | snp | C/T | 5.12501e-05 | 0.00506186 | missense | UBE2O | GRCh38.p7 | 17:76399890 | GAGCATGACATGATC[C/T]GCACAACCTGCTTCT | 63893 |
| rs747772680 | snp | A/G | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454538 | GTAACTCTAGGGCCA[A/G]GCGTGGTGGCTCATG | 63893 |
| rs747786239 | in-del | -/CAAAAAAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425225 | TCAAGGTCCTTTCGA[-/CAAAAAAAA]AAAAAAAAAAAAAAA | 63893 |
| rs747798273 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421673 | CCCGGCCCTGAGTGA[C/G]TATTTTCTATTTTCC | 63893 |
| rs747894720 | snp | A/G | 1.70577e-05 | 0.00292037 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400503 | GTCCGTGCCCCCTGG[A/G]CAGAAACTCTTGGTA | 63893 |
| rs747909060 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415106 | CAGGCTGCGGTCCTG[C/T]GGCTGCCGGGCATCC | 63893 |
| rs747935394 | in-del | -/GCT | 2.11741e-05 | 0.00325371 | intron-variant | UBE2O | GRCh38.p7 | 17:76395966 | GACTTCCCACTCGCC[-/GCT]GCTGGCCTCAGCACT | 63893 |
| rs747956830 | snp | A/G | 4.9445e-05 | 0.00497193 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398907 | CACAGGGAAGAGGTC[A/G]TTGGAGCGGATGTTG | 63893 |
| rs748012864 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446753 | CAGAAATGCCAGTTA[C/T]GTGGAGTGTCTGCAC | 63893 |
| rs748038435 | snp | C/G | 3.31713e-05 | 0.00407242 | missense | UBE2O | GRCh38.p7 | 17:76396532 | GGCCCGTCCTTGCCA[C/G]CCTTCTCCATCAGCC | 63893 |
| rs748096093 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403373 | CTTTGGGCTCAAGCG[A/T]CTCTCCCACCTCAGT | 63893 |
| rs748242690 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419107 | TGGGCAACCTAGTGA[C/G]ACCCTATCTCTACAG | 63893 |
| rs748299911 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407607 | ACGCAGACACAGACC[A/T]AAATCAGTGCCGTCA | 63893 |
| rs748312467 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450374 | GAGCTACCTATCAGG[C/T]ATAAACTCCACCCTC | 63893 |
| rs748382543 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393944 | TGCACTACTTTTCTT[C/T]TCCTGAGTGAGATGT | 63893 |
| rs748403647 | snp | C/G | 1.69129e-05 | 0.00290795 | intron-variant | UBE2O | GRCh38.p7 | 17:76395699 | CACACAGCACATCTG[C/G]ACCTGCCCATGCCAA | 63893 |
| rs748432889 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449308 | GGCAAGGCACTGTGG[A/C]TTATGCCTGTAATTC | 63893 |
| rs748438911 | in-del | -/GTA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435254 | TAAAATATAAAAAAG[-/GTA]GTATACTCACACACA | 63893 |
| rs748450877 | snp | A/G | 1.68562e-05 | 0.00290307 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396165 | GAAGACCTCGCCCTT[A/G]GCGCTGGTGAAGGTG | 63893 |
| rs748516397 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440672 | ATTGTATCTCTATTT[C/T]TCAGGATCCTTCCAG | 63893 |
| rs748529528 | snp | C/T | 3.29549e-05 | 0.00405911 | intron-variant | UBE2O | GRCh38.p7 | 17:76398462 | AGCAAGCAGTAGGGG[C/T]TGCACACACCTCCAC | 63893 |
| rs748531345 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76398047 | GCTCAAGAAGCCTGA[C/T]CCCAGAAGGGAGGCA | 63893 |
| rs748537220 | snp | C/G | 0.000152381 | 0.00872739 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452920 | CACCAGCCCGAAGTG[C/G]ACGGAGCCACGGTAA | 63893 |
| rs748546091 | in-del | -/CT | 1.64779e-05 | 0.00287031 | intron-variant | UBE2O | GRCh38.p7 | 17:76402596 | TCTCTGGTGGTGAGA[-/CT]CTACCTGGCGCCGTT | 63893 |
| rs748568657 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442204 | TGGGGAGCCCGCGAC[A/G]GAAGTTGCCAAAGTA | 63893 |
| rs748600590 | snp | C/T | 3.37342e-05 | 0.00410682 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391318 | AGCTGGGGGCTCTGG[C/T]GAGCTGCTGGCCTTG | 63893 |
| rs748646026 | snp | G/T | 1.67775e-05 | 0.00289629 | intron-variant | UBE2O | GRCh38.p7 | 17:76400997 | CCATCTCCTACCCTT[G/T]GGCCCGGACCCACCT | 63893 |
| rs748647369 | snp | A/G | 3.38553e-05 | 0.00411418 | intron-variant | UBE2O | GRCh38.p7 | 17:76401157 | CGAAGAAGAGACCCT[A/G]CGGGATGTGGGGCCA | 63893 |
| rs748650776 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432257 | CCGTCAAACTGCTAC[A/G]GAAAGGACTCAGTTA | 63893 |
| rs748651450 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443087 | TAGCAGGAGTTAGTA[A/C]CAGACATAATTCAGG | 63893 |
| rs748676202 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427690 | CAGCTCGGGCATTCC[-/T]TGCAACATGTAGATG | 63893 |
| rs748686473 | snp | A/G | 1.67234e-05 | 0.00289161 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391396 | TTCCAGCCAGGACTC[A/G]ATACGGTTCACCAGC | 63893 |
| rs748721654 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395623 | GAGTGTCCTCGCAGG[C/T]GCCAGTCAGCCCCGG | 63893 |
| rs748750993 | snp | G/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389957 | AAAAGCTTAGAAAAC[G/T]TGTAAACCTCTGGGC | 63893 |
| rs748771734 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445708 | GGCAAATAACTTGGA[A/G]TAGATAAATCCAGAG | 63893 |
| rs748787903 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398351 | GTGGTCAGCAATGTC[A/G]TAAACACTCACATCT | 63893 |
| rs748795835 | snp | C/T | 1.71108e-05 | 0.00292491 | intron-variant | UBE2O | GRCh38.p7 | 17:76400116 | GGCCAGTTCCTCAAA[C/T]GCCCACCAATCCCCA | 63893 |
| rs748804237 | snp | C/G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401967 | CCTTTTCTAGGAAAC[C/G/T]GCTCTGTTTAGCTGG | 63893 |
| rs748843692 | in-del | -/C | 1.73411e-05 | 0.00294453 | intron-variant | UBE2O | GRCh38.p7 | 17:76401191 | GAAAGTCCCCGTGAG[-/C]GGTGTCTCCATGGGT | 63893 |
| rs748876884 | snp | C/T | 1.85448e-05 | 0.003045 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390929 | GGTGATGCTCTTTCC[C/T]CTGTGCCTGGCAGCT | 63893 |
| rs748935218 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434575 | CTCGTCCTGGGGAAA[C/G]GCAACAGAACCCACC | 63893 |
| rs748935807 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420721 | AAGGAGGAAGAGACA[C/G]AAGACGTCCTGGGAT | 63893 |
| rs748969638 | snp | C/T | 6.91718e-05 | 0.00588057 | intron-variant | UBE2O | GRCh38.p7 | 17:76398615 | AAGGGAAGTGACTAG[C/T]TAAGGGATCCCGGCT | 63893 |
| rs749021534 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | UBE2O | GRCh38.p7 | 17:76399412 | CTGCCTGGCTTCACG[C/T]TGACGCCATTGGGGA | 63893 |
| rs749050041 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425979 | TCTCCTCCCCACAAG[A/G]GGTTCACAGGAGGCA | 63893 |
| rs749080271 | snp | C/T | 3.37844e-05 | 0.00410987 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396639 | GTCCTCAGGGGCCAC[C/T]GGCTGCTCCAGGGGT | 63893 |
| rs749090531 | snp | A/G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443432 | TAGCTGGGATCACAG[A/G/T]CACCCACCACCACGC | 63893 |
| rs749110407 | snp | C/T | 1.67156e-05 | 0.00289093 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396753 | TTCATCCGAGGATGC[C/T]CCGCTGGTGCTGCCT | 63893 |
| rs749142929 | snp | A/G | 1.64795e-05 | 0.00287045 | missense | UBE2O | GRCh38.p7 | 17:76402692 | ATGTAGTCCCCATAC[A/G]TGAAGGGCTGCAGAC | 63893 |
| rs749167261 | snp | A/C | 0.000116305 | 0.0076249 | intron-variant | UBE2O | GRCh38.p7 | 17:76391849 | TCAATTCTGTTCCCC[A/C]GGCCCCTATCCACCA | 63893 |
| rs749173456 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404361 | GCAGAGCTCTGCGGC[A/G]GGCCTGCCAAGAACA | 63893 |
| rs749203435 | in-del | -/ACC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429637 | TCTGGACAGGTGAGG[-/ACC]ACATTAGATGGAGTA | 63893 |
| rs749207332 | in-del | -/CATA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435415 | ATACACACACACACA[-/CATA]CACACACACACACAC | 63893 |
| rs749237308 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414984 | CCTCAAAAGTATAAG[G/T]AGAAGGCAGAAAAGT | 63893 |
| rs749257345 | snp | A/G | 3.56525e-05 | 0.00422197 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391964 | CCCATTGTCATACAG[A/G]TTGGGGTTCAGGCGG | 63893 |
| rs749300880 | snp | A/G | 1.66863e-05 | 0.0028884 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405230 | CTGCAGGTCCTTGCT[A/G]TTGACGGGATAGATG | 63893 |
| rs749311754 | snp | C/T | 1.65455e-05 | 0.00287619 | missense | UBE2O | GRCh38.p7 | 17:76397858 | CCACCTTGCTGCTGA[C/T]GTCCACACGGGCCAC | 63893 |
| rs749326133 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432184 | CTCAAGGCCCCCTAT[C/T]GCCAGGCACACACAC | 63893 |
| rs749360768 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76398187 | AGCCACCTGGTGGCA[G/T]CATCAGGGACTGCAG | 63893 |
| rs749406601 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448015 | TTCATTGCAGAGGGA[A/G]AAAATGAGGCAGTGA | 63893 |
| rs749442267 | snp | C/G/T | 3.31029e-05 | 0.00406823 | intron-variant | UBE2O | GRCh38.p7 | 17:76395880 | GAGGGGGGAAGAGAA[C/G/T]AGTCAGTCCCTCATG | 63893 |
| rs749448510 | snp | A/G | | | missense | UBE2O | GRCh38.p7 | 17:76396503 | CCTCTTTCAACTCCC[A/G]GAAGCTCTTGGGTGG | 63893 |
| rs749452583 | snp | A/T | | | missense | UBE2O | GRCh38.p7 | 17:76399810 | CCGCTTCGCTCTTGG[A/T]TTTGGATTCCCCCTT | 63893 |
| rs749483780 | snp | A/G | 0.000199216 | 0.0099784 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405513 | GGACGCAGGACTCAC[A/G]GTGGATCGCATGTGC | 63893 |
| rs749507682 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438414 | ATCACCTCAAAGCCC[-/T]TGGCACACTAATGTC | 63893 |
| rs749532176 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421478 | TCAAGCGATTGTCCT[C/G]CCTCAGCCTCACAAG | 63893 |
| rs749534354 | snp | A/G | 2.8883e-05 | 0.00380008 | intron-variant | UBE2O | GRCh38.p7 | 17:76396020 | TTGCCCTGGGGCAGT[A/G]GCTGGGGTCTGGCGA | 63893 |
| rs749618723 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411003 | TGAAAATACAAAGAC[A/G]CTAAATAAAGAAGCT | 63893 |
| rs749725743 | snp | A/T | 1.65023e-05 | 0.00287244 | missense | UBE2O | GRCh38.p7 | 17:76391496 | TGGGTCATGGACTGC[A/T]CCACGCGGATCAGCG | 63893 |
| rs749735403 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438452 | CTGCTCTGTCTCCCA[A/C]CTCCCCCACTACACC | 63893 |
| rs749767902 | snp | A/G | 3.38215e-05 | 0.00411213 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402070 | GCACACTACCGAGTC[A/G]CTGACGTGCGGGCAG | 63893 |
| rs749793750 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442153 | GACACCAGCTCTAGC[G/T]AGCTCTAGCCTAGTC | 63893 |
| rs749809087 | snp | A/G | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454199 | TATAAAAAGTAGGCC[A/G]GGCGCGGCAGCTCAC | 63893 |
| rs749838228 | snp | G/T | 1.65348e-05 | 0.00287526 | intron-variant | UBE2O | GRCh38.p7 | 17:76397781 | AAGCTCAGCAGGGGG[G/T]TCTTGCCAGAGCCTC | 63893 |
| rs749846160 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441427 | TGGCGGATGATGAGT[C/T]CGCCTCATCCCTTTC | 63893 |
| rs749869260 | in-del | -/ACAAAAAAAAAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425224 | CTCAAGGTCCTTTCG[-/ACAAAAAAAAAAA]AAAAAAAAAAAAAAG | 63893 |
| rs749873487 | snp | C/G/T | 4.29943e-05 | 0.00463634 | intron-variant | UBE2O | GRCh38.p7 | 17:76395967 | ACTTCCCACTCGCCG[C/G/T]TGCTGGCCTCAGCAC | 63893 |
| rs749896292 | snp | A/G | 8.41971e-05 | 0.00648779 | intron-variant | UBE2O | GRCh38.p7 | 17:76400341 | GGGCTGGACTCCTGG[A/G]AGGCCAGCAGTGTTC | 63893 |
| rs749904417 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426848 | ATACCATTACTGTCC[A/G]CATTTCTCCTTTCTC | 63893 |
| rs749923110 | snp | C/T | 1.65784e-05 | 0.00287905 | missense | UBE2O | GRCh38.p7 | 17:76391017 | TCAGGACACCCCGGA[C/T]GCTCTTGATGAAACC | 63893 |
| rs749954241 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440484 | AGGCGTAAGCTGCCA[C/T]GCTAAGATGATTTCT | 63893 |
| rs749955936 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397484 | GGGTGGTAGGAAAGT[C/T]TCCATCTCCTTTTAG | 63893 |
| rs749991958 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395003 | GCCTCAGTCTCCCGA[A/G]TAGCTGGGATTACTG | 63893 |
| rs750013336 | snp | A/C | 1.65231e-05 | 0.00287424 | missense | UBE2O | GRCh38.p7 | 17:76391140 | TCACACTGGGTGGCA[A/C]CGATGCGTCTGGTGC | 63893 |
| rs750033867 | snp | C/G | 5.11539e-05 | 0.00505711 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400470 | CTGGGTGATGACAGA[C/G]GGTGGGGGGCTGACG | 63893 |
| rs750044994 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415764 | AGCTGAGATCACGCC[A/G]CTGCACTCCAGCTTG | 63893 |
| rs750123879 | snp | C/T | 0.00021452 | 0.0103544 | missense | UBE2O | GRCh38.p7 | 17:76398954 | CCTGCCACATCACGT[C/T]GGCTGAGGTCATCGT | 63893 |
| rs750135296 | in-del | -/AAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419284 | GTAAGACCCTATCTC[-/AAA]AAAAAAAAAAAAAAA | 63893 |
| rs750185602 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407389 | CTCCACTCTGAGATA[C/T]GGCATTTTTTTGTGC | 63893 |
| rs750201170 | snp | A/G | 1.66112e-05 | 0.00288189 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391582 | GTCGAAGCCGGCTTC[A/G]TTGTAGTATGGTTCA | 63893 |
| rs750231248 | snp | C/T | | | missense | UBE2O | GRCh38.p7 | 17:76392044 | TGTTGGGGAGCTGGA[C/T]GTCAAACAAGTAGAG | 63893 |
| rs750298228 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408424 | AAGAGAAAATAAGCA[A/G]CTCATTCAATGTCAC | 63893 |
| rs750311893 | snp | A/G | 8.26398e-05 | 0.00642753 | missense | UBE2O | GRCh38.p7 | 17:76397830 | GTCTTTGAGTTGTCA[A/G]CCCACACCACCTCCA | 63893 |
| rs750312229 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409630 | CCAACTCCTGACCCC[A/G]TGACCTGCCCTCCTC | 63893 |
| rs750374705 | snp | C/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451405 | ACATTTCTCTGAGGG[C/G]AAGCAGGGTCCTGTG | 63893 |
| rs750401785 | snp | A/G | 4.9606e-05 | 0.00498002 | intron-variant | UBE2O | GRCh38.p7 | 17:76395867 | GAATGATTTGCTAGA[A/G]GGGGGAAGAGAATAG | 63893 |
| rs750410011 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434594 | ACAGAACCCACCTTA[C/T]ATGGCCGTGGTTTGC | 63893 |
| rs750434101 | snp | C/T | 7.02691e-05 | 0.00592703 | intron-variant | UBE2O | GRCh38.p7 | 17:76405484 | GGCTGCCCCCAGGCC[C/T]GGGGCTGGGGTGGGG | 63893 |
| rs750511226 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403339 | CAATGGTGTGATCTT[G/T]GCTTAATGCAACCTC | 63893 |
| rs750516021 | snp | A/G | 1.78768e-05 | 0.00298966 | intron-variant | UBE2O | GRCh38.p7 | 17:76399934 | CACCTGCAAGGGCGG[A/G]GCAGAGAGGACAGGG | 63893 |
| rs750518226 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | UBE2O | GRCh38.p7 | 17:76398289 | GCCCCATCCTCAGTA[C/T]TGCCGATGCGGATGA | 63893 |
| rs750527209 | snp | A/C | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453977 | TTAACTTATTTTCAT[A/C]TTAATTTGCTCATCT | 63893 |
| rs750570774 | in-del | -/AGGG | 0.00163655 | 0.0285586 | intron-variant | UBE2O | GRCh38.p7 | 17:76392120 | GAAGAGGTCCTAGGT[-/AGGG]AGGGAGGGAGGGAGG | 63893 |
| rs750593364 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76396118 | GAAGACCAGGCAAGG[A/G]CTGACTCACAGGGTG | 63893 |
| rs750596537 | snp | C/G | 0.000562588 | 0.0167624 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452829 | CGTGGCCCGCGCCCC[C/G]GGCCTCGGAGCACCC | 63893 |
| rs750608032 | snp | C/T | 3.29506e-05 | 0.00405884 | intron-variant | UBE2O | GRCh38.p7 | 17:76398421 | ATGAGCTAGGGGTCC[C/T]ACACCCAACCCCAGA | 63893 |
| rs750647778 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442873 | GCTACACAGTGCAGG[C/T]ATGAGGCAAGCAGAG | 63893 |
| rs750656396 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441996 | GCCTCGTTCGTACTT[A/T]GCCATCCTCCTAAGG | 63893 |
| rs750683169 | snp | C/G | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390867 | GGGGCATGGGAAGAG[C/G]GGTGATTCCGGGGGG | 63893 |
| rs750686120 | snp | A/G | 1.69392e-05 | 0.00291021 | intron-variant | UBE2O | GRCh38.p7 | 17:76400966 | GCTCAGCTCCAGGGT[A/G]TGGAGGTCAAGGACT | 63893 |
| rs750688444 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412853 | TCTCTATTAAAAATA[A/C]AAAAATTACCTGGGC | 63893 |
| rs750731052 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404213 | ATAATCTGGGACTAC[A/G]TTCCCACAAAATACA | 63893 |
| rs750760266 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447405 | AAGTAAAACATCTAA[A/T]GCACTAAGAGTGCCT | 63893 |
| rs750765625 | snp | A/G | 1.68778e-05 | 0.00290493 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396594 | CTGGACGGCAGCTGT[A/G]GCTGCCTCTTCACTG | 63893 |
| rs750779586 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435622 | GTGCTGAGCCCTCTC[A/G]AAGGTGATCTCGTGC | 63893 |
| rs750832592 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446325 | ATTCATGTTATACAC[A/G]ACAATTGCACCCTTT | 63893 |
| rs750841720 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403106 | TGCTCTGAGTAAATA[C/T]GTTAACACATCAAGG | 63893 |
| rs750919899 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445832 | TGGCTCCTGACAGAG[-/T]CCCCCCGTGGCTGGC | 63893 |
| rs750941760 | snp | A/G | 1.71018e-05 | 0.00292414 | intron-variant | UBE2O | GRCh38.p7 | 17:76391888 | TCCTCCTTCTTGGCT[A/G]GGGGCCTGGCCCTAT | 63893 |
| rs750974977 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392152 | GGCCAAGGTTGGCAG[C/G]GGTGGAAGGGGGTGT | 63893 |
| rs750978218 | snp | C/T | 1.76655e-05 | 0.00297194 | intron-variant | UBE2O | GRCh38.p7 | 17:76405172 | GAGAACCAGAGGGCC[C/T]AGAAAGGATGATGAG | 63893 |
| rs750993705 | snp | C/T | 1.66128e-05 | 0.00288204 | missense | UBE2O | GRCh38.p7 | 17:76391257 | CTCCTGGGGCTGGCC[C/T]TCCATCCTCAGGTTC | 63893 |
| rs751032129 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438998 | GCCGCCAAATCACCC[A/G]TTGTAAACTCTGATG | 63893 |
| rs751087303 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438391 | TAAAGGCTCCTCGTC[A/G]CTCTTCTGATCACCT | 63893 |
| rs751168646 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407295 | AAGACCCCAGGAGGC[A/T]GGAGAGGCATGCTGG | 63893 |
| rs751262022 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432915 | ACTAGGATGGCTATA[A/T]ACAAAGTGACAGTCA | 63893 |
| rs751273744 | snp | C/T | 3.29663e-05 | 0.00405981 | missense | UBE2O | GRCh38.p7 | 17:76402654 | TCAAGTCGTAGACCT[C/T]CCCCAGCCAGCAGTC | 63893 |
| rs751416906 | snp | A/G | 8.23757e-05 | 0.00641725 | missense | UBE2O | GRCh38.p7 | 17:76399614 | GAACTGGTGTCGTCC[A/G]TGTCATCAGCAGCCT | 63893 |
| rs751420301 | snp | A/G | 2.75016e-05 | 0.00370811 | intron-variant | UBE2O | GRCh38.p7 | 17:76396007 | ACAGGGAAATGGTTT[A/G]CCCTGGGGCAGTAGC | 63893 |
| rs751450114 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448977 | GAAGCATATAAGAGA[C/T]ACTGGCCACTAGCTC | 63893 |
| rs751455157 | in-del | -/G | 1.65351e-05 | 0.00287528 | intron-variant | UBE2O | GRCh38.p7 | 17:76395866 | GAATGATTTGCTAGA[-/G]GGGGGGAAGAGAATA | 63893 |
| rs751461817 | snp | A/C | 2.13113e-05 | 0.00326423 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452709 | GCCCGCGCCGCCCAG[A/C]CCCCGCCCGCCGCAC | 63893 |
| rs751508295 | snp | A/G | 2.08019e-05 | 0.00322498 | intron-variant | UBE2O | GRCh38.p7 | 17:76396100 | GAGAAGGCGGGGGAA[A/G]GCGAAGACCAGGCAA | 63893 |
| rs751511677 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417959 | TAGAGGAGCTGCTTG[C/T]TGCTGTTGTGCCTTG | 63893 |
| rs751511764 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405829 | GGCACTTGGCTTGCC[A/G]GAGGTAGCCTTCCTC | 63893 |
| rs751583769 | snp | C/T | 1.70032e-05 | 0.0029157 | missense | UBE2O | GRCh38.p7 | 17:76400486 | GGTGGGGGGCTGACG[C/T]TGTCCGTGCCCCCTG | 63893 |
| rs751611192 | in-del | -/TG | 1.80595e-05 | 0.0030049 | intron-variant | UBE2O | GRCh38.p7 | 17:76399951 | CAGAGAGGACAGGGC[-/TG]TGAGGTGCACCTGGG | 63893 |
| rs751731637 | snp | C/T | 1.67354e-05 | 0.00289265 | missense | UBE2O | GRCh38.p7 | 17:76401132 | CCTGGGTAGAAGCCA[C/T]AGGAATCATCGAAGA | 63893 |
| rs751745147 | snp | A/G | 1.6537e-05 | 0.00287545 | missense | UBE2O | GRCh38.p7 | 17:76391470 | AGACCTCGGGGGGCC[A/G]CCGCACCAGCTGGGT | 63893 |
| rs751759639 | snp | C/T | 3.29576e-05 | 0.00405928 | missense | UBE2O | GRCh38.p7 | 17:76396299 | CGTCGGGCACTGCTT[C/T]CATCTTCTCCTCCTC | 63893 |
| rs751773686 | snp | A/C | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451690 | ACCTCCCAAGGACCT[A/C]AAACAGCGTAGGCCT | 63893 |
| rs751781270 | in-del | -/AGTG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76402169 | TCCACCAGGGGACAC[-/AGTG]AGTACCAAAAAGTTG | 63893 |
| rs751799376 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453944 | CCACTTACTAATCTA[C/T]AAAAATAGGCACACT | 63893 |
| rs751812510 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401232 | TCCACGCCTGTGCCC[A/G]CTGGCTGCCCACCTG | 63893 |
| rs751817694 | snp | A/C | 1.64732e-05 | 0.0028699 | missense | UBE2O | GRCh38.p7 | 17:76399523 | TAAGTTCTTGATGGA[A/C]AAGGGGATGCTCTTT | 63893 |
| rs751819366 | snp | A/G | 1.76602e-05 | 0.0029715 | intron-variant | UBE2O | GRCh38.p7 | 17:76402027 | CCAGAGGACTGAGCA[A/G]TCAGAGAAGGGTGCT | 63893 |
| rs751919957 | snp | C/T | 1.74363e-05 | 0.0029526 | missense | UBE2O | GRCh38.p7 | 17:76391926 | TTTCCAATCCAGGTG[C/T]CCAGGAGGCTGACAC | 63893 |
| rs751931605 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414681 | GCCTGCCCGAGGGAC[A/G]GAGAAAGGGGACTGA | 63893 |
| rs751998179 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434775 | CTTTTTCACTTAAGC[-/T]TTTTTTTTTTTTTTT | 63893 |
| rs752102546 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446257 | AACTCTGAGGGGACC[C/G]ACCACCAGCGGCAGC | 63893 |
| rs752134380 | snp | C/T | 1.6495e-05 | 0.0028718 | missense, intron-variant | UBE2O | GRCh38.p7 | 17:76400203 | CTGGACATTCCCAGG[C/T]AATCTTGGCTGGCTC | 63893 |
| rs752145576 | snp | C/G | 1.6476e-05 | 0.00287014 | intron-variant | UBE2O | GRCh38.p7 | 17:76398435 | CTACACCCAACCCCA[C/G]AGCCCACCTGAAGCA | 63893 |
| rs752149532 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445465 | CCAAAAAGGACATTC[A/G]TTCCAATCCTTATTG | 63893 |
| rs752169017 | in-del | -/AA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435511 | GACAAGCTAATTCGC[-/AA]TATTCCCCCCGTTTA | 63893 |
| rs752224956 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447882 | CTGGCTCTCTCTGAC[A/G]GACATCAGAATGCTG | 63893 |
| rs752229286 | snp | C/T | 1.66189e-05 | 0.00288256 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396744 | ATCTTCCCATTCATC[C/T]GAGGATGCCCCGCTG | 63893 |
| rs752235323 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399487 | AGTGATTTTATTCTT[C/T]TTCCTCTTGTGTTTG | 63893 |
| rs752272168 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400912 | CAGATGCTGAGGAGC[A/G]GGGCTCAACCCTCAA | 63893 |
| rs752287440 | in-del | -/CTT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409400 | AATGAACACACACTA[-/CTT]CTTTTTTTTTTTTTG | 63893 |
| rs752300414 | snp | C/T | 1.7238e-05 | 0.00293576 | intron-variant | UBE2O | GRCh38.p7 | 17:76405198 | ATGAGAAGACAGGGC[C/T]GGCTCACCCAGATGT | 63893 |
| rs752302605 | in-del | -/TATATACGTATGTGTATACATATGTACACACACGTA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415996 | ATATGCACATACACG[lengthTooLong]TATATGTGTGTGTAC | 63893 |
| rs752321377 | snp | C/T | 1.87608e-05 | 0.00306269 | intron-variant | UBE2O | GRCh38.p7 | 17:76396869 | GACAGGAAGTCACCT[C/T]CCCACCACTAAGGAG | 63893 |
| rs752330855 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438291 | CAATGGGAATGTACT[C/T]AATGGCACTGAACTG | 63893 |
| rs752390284 | snp | A/G | 6.62219e-05 | 0.00575383 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405281 | CTTGACGGCACAGTC[A/G]ATGTTGACGTCGATC | 63893 |
| rs752397602 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442765 | TGACACAATCCAGGC[A/G]ATCACTTGGGAGGTC | 63893 |
| rs752404070 | snp | A/C/G | 0.000157552 | 0.00887444 | intron-variant | UBE2O | GRCh38.p7 | 17:76392125 | GGTCCTAGGTAGGGA[A/C/G]GGAGGGAGGGAGGCC | 63893 |
| rs752421229 | snp | C/T | | | missense | UBE2O | GRCh38.p7 | 17:76398516 | TGAACCACTTCACCA[C/T]GCAGGTACGGCCGAT | 63893 |
| rs752424654 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393637 | TCAAGCTGAAAGGCA[C/G]TTCCAGGCTGGTGAG | 63893 |
| rs752432724 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76437037 | ACCCATAATCCTAGC[C/T]GCTCAGGAGGCTGAG | 63893 |
| rs752457692 | snp | A/G | 2.02218e-05 | 0.0031797 | intron-variant | UBE2O | GRCh38.p7 | 17:76396103 | AAGGCGGGGGAAGGC[A/G]AAGACCAGGCAAGGG | 63893 |
| rs752465640 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418202 | TCAGCCTTCTGACAA[-/T]TGTTTTCTATACTAT | 63893 |
| rs752475733 | in-del | -/TTTA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427330 | TTTCACTCTAGAGGC[-/TTTA]TTTGATTCTTTAAAA | 63893 |
| rs752503430 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430135 | GTACCAACATTTCAG[C/T]CTCTGCTCTGCTCAG | 63893 |
| rs752504556 | in-del | -/T | 1.74051e-05 | 0.00294996 | intron-variant | UBE2O | GRCh38.p7 | 17:76400434 | CTGGCAGTAAGGGCA[-/T]GCTTACCTGCCTAGG | 63893 |
| rs752536750 | snp | C/T | 8.39666e-05 | 0.00647891 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452814 | TGGCCCGGCCCTCCT[C/T]GTGGCCCGCGCCCCC | 63893 |
| rs752541784 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411844 | GCACATGCCACCACC[C/T]GGCTAATTTTATTTT | 63893 |
| rs752543834 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397661 | AGGGCTGTGTGGAAT[G/T]CCTGCCTTTCCCCTC | 63893 |
| rs752545386 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441947 | GTTCCTGATTCATTT[A/G]CAGTCGGGTGGGGCA | 63893 |
| rs752582557 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392423 | GTGTGGGCCACCGTG[A/C]CCAGATGATTTTTTT | 63893 |
| rs752608177 | snp | C/G | 3.33017e-05 | 0.00408041 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76401059 | GCTGAGCACGGGCTT[C/G]ACACCTGACAGCCAC | 63893 |
| rs752624995 | snp | C/T | 2.81599e-05 | 0.00375222 | intron-variant | UBE2O | GRCh38.p7 | 17:76400591 | AGTCAGGGCAGGCTC[C/T]GACAGCACTCTCTTT | 63893 |
| rs752632303 | in-del | -/TATA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416030 | ATATGTACACACACG[-/TATA]TATGTGTGTGTACAT | 63893 |
| rs752633351 | snp | G/T | 3.35965e-05 | 0.00409843 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391372 | GGCCTTCTCCAGCAG[G/T]GCATGGGTTTCCAGC | 63893 |
| rs752648846 | in-del | -/TTC | 0.000115343 | 0.0075933 | cds-indel | UBE2O | GRCh38.p7 | 17:76399482 | TCTCGAGTGATTTTA[-/TTC]TTCTTCCTCTTGTGT | 63893 |
| rs752654700 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431712 | GCTGGGAAGCCCAGC[C/G]GGGGGGACTGCTTGA | 63893 |
| rs752672212 | in-del | -/AGGATG | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389034 | AGAATGTGGCAGGGA[-/AGGATG]AGGATCCATCCAAGT | 63893 |
| rs752756709 | snp | A/G | 1.64784e-05 | 0.00287035 | intron-variant | UBE2O | GRCh38.p7 | 17:76402592 | TGGCTCTCTGGTGGT[A/G]AGACTCTACCTGGCG | 63893 |
| rs752808182 | snp | C/G | 5.16116e-05 | 0.00507968 | intron-variant | UBE2O | GRCh38.p7 | 17:76402143 | CTAAAACAGAGAACA[C/G]AGGTTTGGTCTCCAC | 63893 |
| rs752814930 | snp | A/G | 1.71129e-05 | 0.00292509 | intron-variant | UBE2O | GRCh38.p7 | 17:76402053 | GTGCTGGCCTGGATG[A/G]AGCACACTACCGAGT | 63893 |
| rs752839250 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419284 | GTAAGACCCTATCTC[-/A]AAAAAAAAAAAAAAA | 63893 |
| rs752881580 | snp | C/G | 5.03512e-05 | 0.00501728 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391609 | TTCATTTACCAGGAT[C/G]AGACCTGTGTGGGCG | 63893 |
| rs752900798 | in-del | -/TA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435406 | ATATACAGATACACA[-/TA]CACACACACATACAC | 63893 |
| rs752959461 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413179 | TACACATATGGTCTT[C/T]AAAGATTTTGCAAGA | 63893 |
| rs752963483 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | UBE2O | GRCh38.p7 | 17:76395799 | CCATCTCCTTCCGCA[C/T]TGTGCTGAAGAACTT | 63893 |
| rs752978918 | in-del | -/C | 0.000481788 | 0.0155133 | intron-variant | UBE2O | GRCh38.p7 | 17:76391717 | ACTTTCCTCCACCGG[-/C]CCTCCCTTGTCCGCA | 63893 |
| rs753011633 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412610 | GAGCTTGAAGGGTCT[A/G]GCTCCACGCTGCCAT | 63893 |
| rs753049680 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394377 | TCCGGAAGGATGCAC[C/T]CAGCGCTGCCTCAGT | 63893 |
| rs753050594 | snp | A/G | 1.65094e-05 | 0.00287305 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400231 | CTCTACCTTGGCTGG[A/G]AAGACATACAGACAG | 63893 |
| rs753075861 | snp | A/G | 1.69887e-05 | 0.00291446 | intron-variant | UBE2O | GRCh38.p7 | 17:76398601 | TAGGGAACCAGAGAA[A/G]GGGAAGTGACTAGCT | 63893 |
| rs753088535 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76398028 | GTAAATGTAACCAGC[A/G]GCAGCTCAAGAAGCC | 63893 |
| rs753162146 | snp | A/G | 8.23839e-05 | 0.00641757 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396327 | CTCTACAATGGCCAC[A/G]TTGTCCAGGGTCTTC | 63893 |
| rs753266916 | snp | A/G | 1.68818e-05 | 0.00290527 | intron-variant | UBE2O | GRCh38.p7 | 17:76398808 | ATTGGCGACCACCCT[A/G]CTGGCTGCCCTTCCA | 63893 |
| rs753284361 | snp | C/T | 3.31549e-05 | 0.0040714 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405299 | GTTGACGTCGATCAC[C/T]GTGCCACACTGACTG | 63893 |
| rs753365266 | snp | A/C | 4.85614e-05 | 0.0049273 | intron-variant | UBE2O | GRCh38.p7 | 17:76392141 | GGAGGGAGGGAGGCC[A/C]AGGTTGGCAGGGGTG | 63893 |
| rs753395308 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430045 | GGCCCAAACCTTATT[C/T]CCACCTTGAGTGCCA | 63893 |
| rs753400999 | in-del | -/CCCACAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425971 | TCCTTCTATCTCCTC[-/CCCACAA]GAGGTTCACAGGAGG | 63893 |
| rs753427543 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447698 | GGTTTAATAAAGTCA[A/C]ACCTATAATCCATCT | 63893 |
| rs753433061 | snp | C/T | 1.65282e-05 | 0.00287469 | missense | UBE2O | GRCh38.p7 | 17:76400247 | AAGACATACAGACAG[C/T]GCTCCCCAAGCTGCC | 63893 |
| rs753461922 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404377 | GGCCTGCCAAGAACA[C/T]GTGGGCATGAGGCAA | 63893 |
| rs753467368 | snp | A/G | 1.65236e-05 | 0.00287429 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76395857 | TTTCTTAAAAGAATG[A/G]TTTGCTAGAGGGGGG | 63893 |
| rs753473341 | snp | C/T | 3.52703e-05 | 0.00419927 | intron-variant | UBE2O | GRCh38.p7 | 17:76405475 | CCCTAAGGTGGCTGC[C/T]CCCAGGCCCGGGGCT | 63893 |
| rs753521818 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409939 | GGGGGCCAGCAGAGG[A/G]AGAGCACAGTGAAGA | 63893 |
| rs753550200 | snp | A/G | 0.000201386 | 0.0100326 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391375 | CTTCTCCAGCAGGGC[A/G]TGGGTTTCCAGCCAG | 63893 |
| rs753582561 | in-del | -/TATGG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433441 | AGGGGTGCAGGGAAA[-/TATGG]TATGACTCCTAATGG | 63893 |
| rs753611258 | snp | A/G | 1.68935e-05 | 0.00290628 | missense | UBE2O | GRCh38.p7 | 17:76396634 | CCCTTGTCCTCAGGG[A/G]CCACCGGCTGCTCCA | 63893 |
| rs753617981 | snp | C/T | 1.66463e-05 | 0.00288494 | missense | UBE2O | GRCh38.p7 | 17:76401082 | ACAGCCACTGGACGC[C/T]GGAGAAGATCTTGGC | 63893 |
| rs753704538 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421203 | ACAGTGAGCTCCCTA[A/G]AGCTGAGCCCAACCG | 63893 |
| rs753707427 | snp | A/T | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451577 | ACCCCGCTTTGTAGT[A/T]TGACATGAAACCCCG | 63893 |
| rs753736949 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408658 | GTGGCCACTGACTGC[A/G]GATGCCTGCTAGGCA | 63893 |
| rs753742875 | snp | G/T | 6.58935e-05 | 0.00573955 | missense | UBE2O | GRCh38.p7 | 17:76399507 | TCTTGTGTTTGCGCT[G/T]TAAGTTCTTGATGGA | 63893 |
| rs753752199 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397590 | GCACCCAGAGATGGA[C/T]GTGAAGAGATTGCTG | 63893 |
| rs753835801 | snp | C/G/T | 0.00013236 | 0.00813423 | intron-variant | UBE2O | GRCh38.p7 | 17:76397753 | GGCCCCCGGCCCAAG[C/G/T]TGCCATAGTCACAAG | 63893 |
| rs753860307 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394351 | GGTGGCAGGCAAACG[A/G]GCTTGCCTGTTCCGG | 63893 |
| rs753865817 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440738 | TCCAGCCTACTGCCT[C/G]TTTCTTAAAATTTTA | 63893 |
| rs753925922 | snp | A/G | 0.000181958 | 0.00953656 | intron-variant | UBE2O | GRCh38.p7 | 17:76391738 | CTTGTCCGCACCCCC[A/G]CTTCAGCCCAACTGT | 63893 |
| rs753942240 | snp | C/T | 1.65392e-05 | 0.00287564 | missense | UBE2O | GRCh38.p7 | 17:76399843 | TGTCTGGGTCTTCCA[C/T]GGAATGGTCCCGGGA | 63893 |
| rs753943012 | snp | A/G | 1.64773e-05 | 0.00287026 | missense | UBE2O | GRCh38.p7 | 17:76399749 | TCGTCCTGCATCTCC[A/G]CTGGACTGGCAGAGC | 63893 |
| rs753954096 | snp | G/T | 1.6476e-05 | 0.00287014 | missense | UBE2O | GRCh38.p7 | 17:76402621 | CGCCGTTGGATAGCT[G/T]CAGGATGATCTGGTT | 63893 |
| rs754023189 | snp | A/G | 1.6525e-05 | 0.00287441 | intron-variant | UBE2O | GRCh38.p7 | 17:76398206 | CAGGGACTGCAGCTG[A/G]TGCACAGGGCAGTGA | 63893 |
| rs754071367 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446717 | GAGCTCCTAATGGAG[-/C]TGACCACTTCTGAGG | 63893 |
| rs754129379 | in-del | -/ACACACACAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435408 | TATACAGATACACAC[-/ACACACACAT]ACACACACACACACA | 63893 |
| rs754136965 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393513 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 63893 |
| rs754166650 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436951 | AGCCTGGCCAACATG[C/T]TGAAACCATTTCTAC | 63893 |
| rs754178014 | snp | A/C | 1.67374e-05 | 0.00289282 | intron-variant | UBE2O | GRCh38.p7 | 17:76398827 | GCTGCCCTTCCAGAG[A/C]TGGCACTACCTCGCT | 63893 |
| rs754215942 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422644 | GGGAACAGCCATGGC[G/T]CAAATGTTCCCCCAG | 63893 |
| rs754218354 | snp | C/T | 3.29951e-05 | 0.00406159 | missense | UBE2O | GRCh38.p7 | 17:76391097 | TCAGGTAAGAAGCTC[C/T]GGTAGCTCTTTCTCC | 63893 |
| rs754230366 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440169 | GATGGTTCTCTCTCC[C/T]ATCTAAGTCTCTGAA | 63893 |
| rs754232552 | in-del | -/C | 4.97006e-05 | 0.00498476 | intron-variant | UBE2O | GRCh38.p7 | 17:76391732 | CCTCCCTTGTCCGCA[-/C]CCCCCGCTTCAGCCC | 63893 |
| rs754261379 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392647 | TGTTTTTCCTCATAA[A/C]TCATTACTTTAAGAC | 63893 |
| rs754265766 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396468 | AGTCATGTTCTTGAG[A/G]CTCTCCAGGATCTTG | 63893 |
| rs754278138 | in-del | -/AGGAAAGA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417706 | GCCTTCGACTACAGG[-/AGGAAAGA]AGGAAAGAATGCTAA | 63893 |
| rs754366411 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455174 | CTCACGCCTGAAATC[C/T]CAACACTTTGACTGC | 63893 |
| rs754375679 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412116 | ACCAGCCCCACACTA[C/G]GTCCCTGGTGAGTGT | 63893 |
| rs754526385 | in-del | -/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433552 | TACTAAAAACCACTT[-/G]AACTGCACACTTTAA | 63893 |
| rs754551925 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403350 | TCTTGGCTTAATGCA[A/G]CCTCCATCTTTGGGC | 63893 |
| rs754591622 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435787 | TCGGGAGCCACATTC[C/G]CTGAGCTGAAGGCAC | 63893 |
| rs754607683 | snp | A/G | 3.29489e-05 | 0.00405874 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402660 | CGTAGACCTTCCCCA[A/G]CCAGCAGTCATAGGC | 63893 |
| rs754621962 | in-del | -/AAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435051 | GGCACAAAGGACAAC[-/AAT]GAGGAGAGGAAAGGG | 63893 |
| rs754623704 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392668 | ACTTTAAGACTGTAT[A/T]CCAGCTGGGCGCGGT | 63893 |
| rs754628003 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447860 | GTGATCTTCTGAAGG[C/G]ACAGGGCTGGCTCTC | 63893 |
| rs754634574 | snp | A/G | 1.74738e-05 | 0.00295577 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391934 | CCAGGTGCCCAGGAG[A/G]CTGACACACACCTTC | 63893 |
| rs754636521 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404422 | AGGCTGAGGGTCAAA[C/T]TACTGAATGTATCAC | 63893 |
| rs754741739 | snp | A/G | 0.00010092 | 0.00710281 | intron-variant | UBE2O | GRCh38.p7 | 17:76405502 | GGCTGGGGTGGGGAC[A/G]CAGGACTCACGGTGG | 63893 |
| rs754757335 | snp | C/T | 4.18953e-05 | 0.00457667 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452710 | CCCGCGCCGCCCAGC[C/T]CCCGCCCGCCGCACC | 63893 |
| rs754768986 | snp | C/T | 8.38469e-05 | 0.00647429 | intron-variant | UBE2O | GRCh38.p7 | 17:76396010 | GGGAAATGGTTTGCC[C/T]TGGGGCAGTAGCTGG | 63893 |
| rs754822739 | snp | A/G | 1.65247e-05 | 0.00287438 | missense | UBE2O | GRCh38.p7 | 17:76391145 | CTGGGTGGCACCGAT[A/G]CGTCTGGTGCGGTCT | 63893 |
| rs754864126 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449693 | GGAGGCCGAGGCGGG[C/T]GGATCACCTGAGGTC | 63893 |
| rs754891584 | in-del | -/G | 1.65887e-05 | 0.00287994 | intron-variant | UBE2O | GRCh38.p7 | 17:76395905 | TCATGGAGAGGCCCT[-/G]GGAGCTCCATCTGCC | 63893 |
| rs754907129 | snp | A/C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430116 | CCTTGGTGTTTTTCC[A/C/G]CAGGTACCAACATTT | 63893 |
| rs754936278 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435059 | GGACAACAATGAGGA[C/G]AGGAAAGGGGAGGTG | 63893 |
| rs754940630 | snp | A/G | 3.40287e-05 | 0.0041247 | missense | UBE2O | GRCh38.p7 | 17:76400492 | GGGCTGACGCTGTCC[A/G]TGCCCCCTGGACAGA | 63893 |
| rs754978362 | in-del | -/CTTGGCTGGCTCTAC | 1.64959e-05 | 0.00287188 | cds-indel, splice-donor-variant | UBE2O | GRCh38.p7 | 17:76400207 | ACATTCCCAGGCAAT[-/CTTGGCTGGCTCTAC]CTTGGCTGGGAAGAC | 63893 |
| rs754982202 | snp | C/T | 3.32474e-05 | 0.00407708 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391264 | GGCTGGCCCTCCATC[C/T]TCAGGTTCTTGTTGG | 63893 |
| rs754989642 | in-del | -/AC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411707 | CTTTTTTTTCTTGAG[-/AC]AGGGTCTCACTCTGC | 63893 |
| rs755027709 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443938 | TTAAGAGGGCATGGT[C/T]GGCCAGGCGCGGTAG | 63893 |
| rs755034817 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428710 | TAAGAGATCTTTGTG[A/G]TGATGGAAGAGTTGT | 63893 |
| rs755036827 | snp | C/T | 1.65518e-05 | 0.00287674 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398973 | TGAGGTCATCGTGGT[C/T]ACCACCTCCACTGCC | 63893 |
| rs755037503 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445313 | TCCCAGGTATAGTTA[C/T]GCTATCAATTTAAAC | 63893 |
| rs755044197 | snp | A/G | 1.67981e-05 | 0.00289806 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76401143 | GCCATAGGAATCATC[A/G]AAGAAGAGACCCTGC | 63893 |
| rs755099611 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418338 | CCTGAAAGTAACAGA[C/G]TAAACTGTACTTGGA | 63893 |
| rs755110422 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | UBE2O | GRCh38.p7 | 17:76396311 | CTTCCATCTTCTCCT[C/T]CTCTACAATGGCCAC | 63893 |
| rs755114691 | snp | G/T | 1.67475e-05 | 0.00289369 | missense | UBE2O | GRCh38.p7 | 17:76391391 | TGGGTTTCCAGCCAG[G/T]ACTCGATACGGTTCA | 63893 |
| rs755125524 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446751 | ACAGAAATGCCAGTT[-/A]ACGTGGAGTGTCTGC | 63893 |
| rs755200941 | snp | A/T | 1.74827e-05 | 0.00295652 | intron-variant | UBE2O | GRCh38.p7 | 17:76402039 | GCAATCAGAGAAGGG[A/T]GCTGGCCTGGATGGA | 63893 |
| rs755212514 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449201 | TTAAGCCTTTACTCA[C/T]TGCCCTCCAATTTAC | 63893 |
| rs755256656 | snp | C/T | 4.94271e-05 | 0.00497102 | missense | UBE2O | GRCh38.p7 | 17:76399639 | CAGCCTCATCATCTG[C/T]GTCCTGCTCTGCCGA | 63893 |
| rs755260792 | snp | A/G | 1.65855e-05 | 0.00287967 | intron-variant | UBE2O | GRCh38.p7 | 17:76397773 | ATAGTCACAAGCTCA[A/G]CAGGGGGGTCTTGCC | 63893 |
| rs755264808 | snp | A/G | 1.73748e-05 | 0.00294739 | intron-variant | UBE2O | GRCh38.p7 | 17:76405191 | AAGGATGATGAGAAG[A/G]CAGGGCCGGCTCACC | 63893 |
| rs755284610 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417277 | CAGCCGAAAGTCAAC[A/G]ACATCCCTGGGCAGC | 63893 |
| rs755346888 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423072 | CAGAATCCCCAATGG[C/T]GGGGCCTGGAGAACA | 63893 |
| rs755358154 | snp | C/G | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454224 | GCTCACACCTGTCAT[C/G]CCAGTACTTTGGGAG | 63893 |
| rs755365755 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422698 | CAGATGTCACCTCCT[C/G]AGAAGGGCTTCTCTG | 63893 |
| rs755388729 | snp | G/T | 1.80902e-05 | 0.00300745 | intron-variant | UBE2O | GRCh38.p7 | 17:76399957 | GGACAGGGCTGTGAG[G/T]TGCACCTGGGCAGGC | 63893 |
| rs755418038 | snp | A/G | 3.78301e-05 | 0.00434898 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390902 | GAGCAGGCGGCGGCT[A/G]GCCTCTCCCACGGTG | 63893 |
| rs755430163 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443033 | AAGATTCAAGCTTAG[A/G]TATTTAGGGGTGAAG | 63893 |
| rs755451502 | in-del | -/GAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395519 | TTTTAAAGGAGGGAG[-/GAAA]GAAAGAACCATCTGG | 63893 |
| rs755483056 | snp | A/G | 3.295e-05 | 0.00405881 | intron-variant | UBE2O | GRCh38.p7 | 17:76398436 | TACACCCAACCCCAG[A/G]GCCCACCTGAAGCAA | 63893 |
| rs755498007 | snp | A/C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424653 | GCCAAGGTGGGAGGA[A/C/T]TGCTTGAGGCCAGGA | 63893 |
| rs755499583 | snp | A/G | 3.38524e-05 | 0.00411401 | intron-variant | UBE2O | GRCh38.p7 | 17:76398596 | TGGACTAGGGAACCA[A/G]AGAAAGGGAAGTGAC | 63893 |
| rs755504180 | snp | C/G | 5.25818e-05 | 0.00512719 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452905 | GCCGTGGATGAGGCG[C/G]ACCAGCCCGAAGTGC | 63893 |
| rs755514402 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420649 | AAACTGGGCTGGGGC[A/G]CTGCAGACATTTCTT | 63893 |
| rs755600627 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412132 | GTCCCTGGTGAGTGT[A/G]TAGACAACAGGTCAG | 63893 |
| rs755610974 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428665 | TATCCAGTTATTCTT[C/G]GCATCCATTCCTATT | 63893 |
| rs755656471 | snp | G/T | 1.69507e-05 | 0.0029112 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405209 | GGGCCGGCTCACCCA[G/T]ATGTGCTGCAGGTCC | 63893 |
| rs755684986 | snp | C/T | 1.76552e-05 | 0.00297108 | missense | UBE2O | GRCh38.p7 | 17:76391953 | ACACACACCTTCCCA[C/T]TGTCATACAGGTTGG | 63893 |
| rs755700294 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416178 | TACACATACGTGTGT[A/G]TGTGTATATGTATAT | 63893 |
| rs755734876 | in-del | -/TCA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419971 | CTCCCTGCCCCTCCT[-/TCA]TCACCTCCCTGCAAC | 63893 |
| rs755757903 | snp | C/T | 1.86218e-05 | 0.00305132 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390924 | CCCACGGTGATGCTC[C/T]TTCCTCTGTGCCTGG | 63893 |
| rs755780950 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434333 | CTGATGTTCCCAGCA[C/T]AGAAAAGGAAAGTGA | 63893 |
| rs755785698 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440024 | CAGTCACTGAGGATA[C/T]AGCAGTGACAGAGAT | 63893 |
| rs755800685 | in-del | -/C | 1.70564e-05 | 0.00292026 | intron-variant | UBE2O | GRCh38.p7 | 17:76401170 | CTGCGGGATGTGGGG[-/C]CAAAGGAAAGTCCCC | 63893 |
| rs755834257 | snp | C/G/T | 3.30372e-05 | 0.0040642 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400240 | GGCTGGGAAGACATA[C/G/T]AGACAGCGCTCCCCA | 63893 |
| rs755843042 | snp | C/T | 9.79384e-05 | 0.00699711 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452821 | GCCCTCCTCGTGGCC[C/T]GCGCCCCCGGCCTCG | 63893 |
| rs755854532 | in-del | -/CGAGGGGA | 3.05125e-05 | 0.0039058 | intron-variant | UBE2O | GRCh38.p7 | 17:76396033 | GTAGCTGGGGTCTGG[-/CGAGGGGA]CTAACCACCCTGCAC | 63893 |
| rs755874632 | snp | C/T | 1.71932e-05 | 0.00293195 | missense | UBE2O | GRCh38.p7 | 17:76400513 | CCTGGACAGAAACTC[C/T]TGGTAATCCATGTAA | 63893 |
| rs755896207 | snp | A/G | 1.66815e-05 | 0.00288799 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391282 | AGGTTCTTGTTGGCC[A/G]GAGTCTGACAGCTCG | 63893 |
| rs755896633 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407457 | ACTTCAAAAAGCCAC[A/G]ATTGCTCCCAGAGAA | 63893 |
| rs755924631 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404001 | TAAGTCCATACTGAT[-/A]AAAAAAAAAGAATAC | 63893 |
| rs755970380 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420087 | TCACCCCTACCCAGC[A/G]CAGCAGTGGCCCCCT | 63893 |
| rs756000381 | snp | A/G | 1.6793e-05 | 0.00289763 | missense | UBE2O | GRCh38.p7 | 17:76391373 | GCCTTCTCCAGCAGG[A/G]CATGGGTTTCCAGCC | 63893 |
| rs756059308 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443232 | TCAATATTTTTTCCT[A/G]TTAAAAAGTTGGGTC | 63893 |
| rs756062083 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392633 | TTATCTTATCAGGTG[-/A]TTTTTCCTCATAAAT | 63893 |
| rs756084287 | snp | A/G | 3.40507e-05 | 0.00412604 | intron-variant | UBE2O | GRCh38.p7 | 17:76402059 | GCCTGGATGGAGCAC[A/G]CTACCGAGTCGCTGA | 63893 |
| rs756088819 | in-del | -/TACACA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435414 | ATACACACACACACA[-/TACACA]CATACACACACACAC | 63893 |
| rs756119498 | snp | C/T | 1.65176e-05 | 0.00287376 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396498 | GATGGCCTCTTTCAA[C/T]TCCCGGAAGCTCTTG | 63893 |
| rs756139115 | snp | A/G | 1.67956e-05 | 0.00289784 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391611 | CATTTACCAGGATCA[A/G]ACCTGTGTGGGCGGG | 63893 |
| rs756167925 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442032 | ACTGGGTGCTGATAA[A/C]CATTCAGGAAACCCA | 63893 |
| rs756174592 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394802 | TTCCATTTCCACTCA[A/T]AGGATCTGTAATGTT | 63893 |
| rs756176989 | snp | A/G | 3.32386e-05 | 0.00407654 | missense | UBE2O | GRCh38.p7 | 17:76396745 | TCTTCCCATTCATCC[A/G]AGGATGCCCCGCTGG | 63893 |
| rs756238650 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412095 | GACCTCAAGGACAAG[C/T]GGACGACCAGCCCCA | 63893 |
| rs756242780 | snp | A/G | 1.7306e-05 | 0.00294155 | intron-variant | UBE2O | GRCh38.p7 | 17:76402150 | AGAGAACAGAGGTTT[A/G]GTCTCCACCAGGGGA | 63893 |
| rs756288445 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399640 | AGCCTCATCATCTGC[A/G]TCCTGCTCTGCCGAG | 63893 |
| rs756294792 | snp | C/T | 1.654e-05 | 0.00287571 | missense | UBE2O | GRCh38.p7 | 17:76397852 | CCACCTCCACCTTGC[C/T]GCTGACGTCCACACG | 63893 |
| rs756315357 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445734 | CAGAGAGTTATCCAG[-/T]AACACAATTCAATTT | 63893 |
| rs756332600 | snp | C/G | 1.64773e-05 | 0.00287026 | missense | UBE2O | GRCh38.p7 | 17:76399741 | CTGCACCCTCGTCCT[C/G]CATCTCCACTGGACT | 63893 |
| rs756382980 | snp | G/T | 1.65438e-05 | 0.00287605 | intron-variant | UBE2O | GRCh38.p7 | 17:76395872 | ATTTGCTAGAGGGGG[G/T]AAGAGAATAGTCAGT | 63893 |
| rs756396119 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76398764 | CCAGATCCACTGCCC[A/G]TTCTCCACAAGCCCC | 63893 |
| rs756396947 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442881 | GTGCAGGCATGAGGC[A/T]AGCAGAGAGCAAACC | 63893 |
| rs756422580 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430538 | GATAACTTGAAGGGC[C/T]ACAGTATAGAGCTCA | 63893 |
| rs756495399 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404220 | GGGACTACGTTCCCA[C/T]AAAATACAATCACTT | 63893 |
| rs756512313 | snp | C/G | 1.70699e-05 | 0.00292142 | intron-variant | UBE2O | GRCh38.p7 | 17:76398604 | GGAACCAGAGAAAGG[C/G]AAGTGACTAGCTAAG | 63893 |
| rs756622298 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422583 | CGGAGGTTCCATCTG[C/T]AATGAAGCCGAGGCA | 63893 |
| rs756627488 | snp | A/G | 3.29663e-05 | 0.00405981 | missense | UBE2O | GRCh38.p7 | 17:76396436 | GAGGTGGGCGAGCCC[A/G]TCAGCAGCTGCTCCA | 63893 |
| rs756652116 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76398108 | CTGAGCGGCAGCTTG[A/C]CTCTGGGGCAGCTGC | 63893 |
| rs756694402 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439012 | CATTGTAAACTCTGA[C/T]GTAAGTCCTCTTTAT | 63893 |
| rs756721426 | snp | A/G | 1.65886e-05 | 0.00287993 | missense | UBE2O | GRCh38.p7 | 17:76405300 | TTGACGTCGATCACC[A/G]TGCCACACTGACTGT | 63893 |
| rs756743218 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436889 | AGTGGCTCATGCCTT[C/T]GAGAGGTCAAGGTGG | 63893 |
| rs756836867 | snp | A/G | 5.49889e-05 | 0.00524323 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390939 | TTTCCTCTGTGCCTG[A/G]CAGCTACTTGTCCTC | 63893 |
| rs756870939 | snp | A/C | 1.73294e-05 | 0.00294353 | intron-variant | UBE2O | GRCh38.p7 | 17:76398618 | GGAAGTGACTAGCTA[A/C]GGGATCCCGGCTAAG | 63893 |
| rs756925063 | snp | A/G | 6.666e-05 | 0.00577283 | missense | UBE2O | GRCh38.p7 | 17:76391001 | GCAGCCCGGAACTGC[A/G]TCAGGACACCCCGGA | 63893 |
| rs756958890 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | UBE2O | GRCh38.p7 | 17:76396355 | TTCTTGAGGTTTTCC[C/T]GTAGCTTCTTGATGT | 63893 |
| rs756960800 | snp | C/T | 1.66746e-05 | 0.00288739 | intron-variant | UBE2O | GRCh38.p7 | 17:76398833 | CTTCCAGAGCTGGCA[C/T]TACCTCGCTTATCTA | 63893 |
| rs756978878 | snp | C/G | 1.66466e-05 | 0.00288496 | missense | UBE2O | GRCh38.p7 | 17:76401084 | AGCCACTGGACGCTG[C/G]AGAAGATCTTGGCAG | 63893 |
| rs757025377 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | UBE2O | GRCh38.p7 | 17:76399515 | TTGCGCTTTAAGTTC[C/T]TGATGGACAAGGGGA | 63893 |
| rs757033675 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416938 | GCTGCGGCTGGTCAC[A/G]TGGAGGCTACACACT | 63893 |
| rs757129683 | snp | C/T | 1.66507e-05 | 0.00288532 | missense | UBE2O | GRCh38.p7 | 17:76405235 | GGTCCTTGCTGTTGA[C/T]GGGATAGATGATGCA | 63893 |
| rs757140729 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438392 | AAAGGCTCCTCGTCG[C/T]TCTTCTGATCACCTC | 63893 |
| rs757169704 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407177 | TGGCACATGGTGCAC[A/G]GTACAGAGTAGGTGC | 63893 |
| rs757225491 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449090 | ACTTTGTTTCTGTTG[C/T]TATTTTCATGAAGGC | 63893 |
| rs757253368 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407366 | CCTGTAACCCTCTGT[G/T]CCCAAATCTCCACTC | 63893 |
| rs757253434 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393726 | ATGGGGGAGGTTGGG[A/G]GACCACCGCTCCACA | 63893 |
| rs757266197 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418183 | AACATGTGAGACCTG[G/T]AACCTCAGCCTTCTG | 63893 |
| rs757278690 | snp | A/T | 1.6528e-05 | 0.00287467 | missense | UBE2O | GRCh38.p7 | 17:76397825 | TGATGGTCTTTGAGT[A/T]GTCAGCCCACACCAC | 63893 |
| rs757283649 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401166 | GACCCTGCGGGATGT[C/G]GGGCCAAAGGAAAGT | 63893 |
| rs757295481 | snp | C/T | 1.65269e-05 | 0.00287457 | intron-variant | UBE2O | GRCh38.p7 | 17:76398207 | AGGGACTGCAGCTGG[C/T]GCACAGGGCAGTGAG | 63893 |
| rs757304780 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405834 | TTGGCTTGCCGGAGG[C/T]AGCCTTCCTCACACT | 63893 |
| rs757323371 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428924 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 63893 |
| rs757324570 | snp | C/T | 1.7011e-05 | 0.00291637 | intron-variant | UBE2O | GRCh38.p7 | 17:76395680 | CTCTTGGGCACTGGG[C/T]GCCCACACAGCACAT | 63893 |
| rs757380373 | snp | A/G | 9.11979e-05 | 0.00675208 | intron-variant | UBE2O | GRCh38.p7 | 17:76396031 | CAGTAGCTGGGGTCT[A/G]GCGAGGGGACTAACC | 63893 |
| rs757386982 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421245 | TGCAGAAAGAAGTGA[C/T]GGCCTGCTGTCAGCG | 63893 |
| rs757426729 | snp | A/G | 3.31752e-05 | 0.00407265 | missense | UBE2O | GRCh38.p7 | 17:76399849 | GGTCTTCCATGGAAT[A/G]GTCCCGGGAACACTG | 63893 |
| rs757427829 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435120 | GCACCAAGCCAGCTG[-/T]TGAGTCACCACGAAG | 63893 |
| rs757460590 | snp | C/T | 3.29506e-05 | 0.00405884 | missense | UBE2O | GRCh38.p7 | 17:76398284 | GAGGAGCCCCATCCT[C/T]AGTATTGCCGATGCG | 63893 |
| rs757460900 | snp | C/T | 3.64578e-05 | 0.00426937 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452726 | CCCGCCCGCCGCACC[C/T]TGGTCTCCTTCACAT | 63893 |
| rs757465246 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397662 | GGGCTGTGTGGAATG[C/G]CTGCCTTTCCCCTCA | 63893 |
| rs757503360 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441152 | AGTGAGATGACACAG[C/G]TAAAGTGTGAGTTAA | 63893 |
| rs757539526 | in-del | -/GC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409839 | TCTGGCACATGCTAA[-/GC]GCCCATTCTCCTGCA | 63893 |
| rs757546901 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant | UBE2O | GRCh38.p7 | 17:76396106 | GCGGGGGAAGGCGAA[A/G]ACCAGGCAAGGGCTG | 63893 |
| rs757641241 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415705 | AGCTACTTAGGAGGC[C/T]GAGGTAGGAGAATTG | 63893 |
| rs757643814 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442732 | ATGACAACCAAGGCA[C/T]GATCAGAGGCTGGGT | 63893 |
| rs757644215 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420370 | ATGGAAGTGCAGGGG[A/G]GCCTATCTTCCCACA | 63893 |
| rs757676811 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445555 | TGCTTTTCACAATAC[C/T]GCTTCAGGAGAACAC | 63893 |
| rs757686476 | in-del | -/TT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421401 | GACGGAGTTTCGCTC[-/TT]TTGTTGCCCAGGCTG | 63893 |
| rs757689409 | snp | C/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390627 | AGGCCCTGGAACACC[C/T]GCCTCTGACCTGAGA | 63893 |
| rs757698260 | in-del | -/TT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440325 | AATTAATTTCATCTC[-/TT]TGTTTTTTTTACTTT | 63893 |
| rs757728570 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435610 | TGGTCAGGTGCTGTG[C/T]TGAGCCCTCTCGAAG | 63893 |
| rs757730913 | snp | A/G | 1.69089e-05 | 0.0029076 | intron-variant | UBE2O | GRCh38.p7 | 17:76391624 | CAGACCTGTGTGGGC[A/G]GGACACCTTCCCTCA | 63893 |
| rs757731628 | snp | A/G | 5.0583e-05 | 0.00502881 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402076 | TACCGAGTCGCTGAC[A/G]TGCGGGCAGACGTCG | 63893 |
| rs757756725 | snp | A/G | 1.65111e-05 | 0.0028732 | intron-variant | UBE2O | GRCh38.p7 | 17:76391752 | CGCTTCAGCCCAACT[A/G]TACCTTGGATGGAGA | 63893 |
| rs757772163 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403194 | AAGGGAGCAGGAAGG[-/A]GAAGAAGGAAGAGGA | 63893 |
| rs757775266 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434251 | CCAGCACACAGTCCT[A/G]TCTCAGAGGTTCAGA | 63893 |
| rs757817683 | snp | A/G | 1.74677e-05 | 0.00295526 | intron-variant | UBE2O | GRCh38.p7 | 17:76402161 | GTTTGGTCTCCACCA[A/G]GGGACACAGTGAGTA | 63893 |
| rs757859829 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434917 | TGAGAAAACCCTGCC[A/C]CAATAGAGGGGCTCG | 63893 |
| rs757877088 | snp | A/G | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389282 | TACAAAAGGCATGCA[A/G]GCAGGTCTGGCAGGC | 63893 |
| rs757878536 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76437060 | AGGCTGAGGCAGGAG[A/G]ATCGCCTGAACCTAG | 63893 |
| rs757878690 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448753 | TGTTCTGCCCAACCA[C/T]GACAGGTGGAGACCA | 63893 |
| rs757907694 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399751 | GTCCTGCATCTCCAC[C/T]GGACTGGCAGAGCCA | 63893 |
| rs757913486 | snp | A/C | 1.77451e-05 | 0.00297863 | intron-variant | UBE2O | GRCh38.p7 | 17:76400398 | GGCCCAGAGCCCTGT[A/C]CCACGCGTGCCCCTG | 63893 |
| rs757949487 | snp | A/G | 1.64885e-05 | 0.00287123 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398868 | GAAGTCTCCAGGGCA[A/G]AACTCGTTGTTGTCC | 63893 |
| rs758047273 | snp | G/T | 1.68559e-05 | 0.00290304 | missense | UBE2O | GRCh38.p7 | 17:76396603 | AGCTGTGGCTGCCTC[G/T]TCACTGATCACCACT | 63893 |
| rs758053854 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394410 | ACATGACTCAGAGAC[A/G]CTAGGCCCCGTCCAC | 63893 |
| rs758055414 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422890 | CCTGGAACACAGAAG[A/G]GTGCCTCTGAGGAGT | 63893 |
| rs758205503 | snp | C/T | 1.65304e-05 | 0.00287488 | missense | UBE2O | GRCh38.p7 | 17:76397831 | TCTTTGAGTTGTCAG[C/T]CCACACCACCTCCAC | 63893 |
| rs758240723 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430286 | AGTTTCTAGGGGAAG[G/T]AGATTTAAATGAATA | 63893 |
| rs758268533 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412923 | TGAGGCAGGAGAATC[C/G]TTTGAACCCGGGAGG | 63893 |
| rs758269729 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409963 | GTGAAGAATTTTAAA[C/T]GTGTGGTCAGGAAAG | 63893 |
| rs758289118 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447923 | ACCAAGTGGCCATCC[G/T]AGGCTTGACCCAGCT | 63893 |
| rs758341069 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416831 | CAGCTCATCTCAGGA[C/T]AGTGAAACAGGACTC | 63893 |
| rs758349656 | in-del | -/AGGG | 0.00163655 | 0.0285586 | intron-variant | UBE2O | GRCh38.p7 | 17:76392119 | GAAGAGGTCCTAGGT[-/AGGG]AGGGAGGGAGGGAGG | 63893 |
| rs758384623 | in-del | -/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407956 | GACAAGGGGCTGGGG[-/G]ATGGTAACATGGTGG | 63893 |
| rs758396527 | snp | A/G | 6.89536e-05 | 0.00587129 | intron-variant | UBE2O | GRCh38.p7 | 17:76405491 | CCCAGGCCCGGGGCT[A/G]GGGTGGGGACGCAGG | 63893 |
| rs758423491 | snp | C/T | 1.83316e-05 | 0.00302745 | intron-variant | UBE2O | GRCh38.p7 | 17:76396120 | AGACCAGGCAAGGGC[C/T]GACTCACAGGGTGCA | 63893 |
| rs758506382 | snp | A/G | 0.000620617 | 0.0176046 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452836 | CGCGCCCCCGGCCTC[A/G]GAGCACCCCGAGCTC | 63893 |
| rs758507673 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451618 | GTCTTTGTCTCCCAC[C/G/T]GTGTGAGAAACCCAG | 63893 |
| rs758513467 | snp | G/T | 1.67203e-05 | 0.00289134 | missense | UBE2O | GRCh38.p7 | 17:76391286 | TCTTGTTGGCCGGAG[G/T]CTGACAGCTCGGCTA | 63893 |
| rs758554592 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429135 | TCGAACTCCTGACCT[C/T]GTGATCTGCCCGCCT | 63893 |
| rs758566479 | snp | C/T | 3.29506e-05 | 0.00405884 | intron-variant | UBE2O | GRCh38.p7 | 17:76398423 | GAGCTAGGGGTCCTA[C/T]ACCCAACCCCAGAGC | 63893 |
| rs758606691 | snp | C/T | 1.64874e-05 | 0.00287113 | missense | UBE2O | GRCh38.p7 | 17:76396239 | CGCTGGGCCACTCAG[C/T]CTTCACAGGTGACTG | 63893 |
| rs758625503 | snp | A/G | 1.64868e-05 | 0.00287109 | intron-variant | UBE2O | GRCh38.p7 | 17:76402570 | GAGGCTATCCTTCCC[A/G]AGCCGATGGCTCTCT | 63893 |
| rs758671409 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401873 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 63893 |
| rs758674294 | in-del | -/AG | 0.0013833 | 0.0262629 | intron-variant | UBE2O | GRCh38.p7 | 17:76402135 | TGGAGCACCTAAAAC[-/AG]AGAACAGAGGTTTGG | 63893 |
| rs758679397 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420300 | GCCAGTTGTTTCCCC[A/G]GGGGCCAAGTTCCCA | 63893 |
| rs758698833 | snp | C/G | 1.6777e-05 | 0.00289624 | missense | UBE2O | GRCh38.p7 | 17:76391379 | TCCAGCAGGGCATGG[C/G]TTTCCAGCCAGGACT | 63893 |
| rs758713064 | snp | A/G | 1.71711e-05 | 0.00293006 | intron-variant | UBE2O | GRCh38.p7 | 17:76399415 | CCTGGCTTCACGCTG[A/G]CGCCATTGGGGAGGG | 63893 |
| rs758767139 | snp | C/T | 1.65072e-05 | 0.00287286 | missense | UBE2O | GRCh38.p7 | 17:76391803 | GACTTGCTTGTCCAC[C/T]TCTCTGTCCCCTGAA | 63893 |
| rs758784960 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433276 | ATAAAAACAAATGAA[A/G]TACTGATACATGCTA | 63893 |
| rs758798133 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420474 | GTTACAGACTCGCCC[A/C]CATCTTTACCCAAAC | 63893 |
| rs758832091 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444233 | CTCACAAACAAAGCA[A/C]AACAAAACAAAACAA | 63893 |
| rs758865506 | snp | A/C/T | 3.29578e-05 | 0.00405931 | missense | UBE2O | GRCh38.p7 | 17:76399768 | GACTGGCAGAGCCAT[A/C/T]GGGCGTCTCCTCAGG | 63893 |
| rs758886804 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445304 | CAGACTGTTTCCCAG[A/G]TATAGTTATGCTATC | 63893 |
| rs758962287 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400890 | GCCCTTTGAGATCAA[C/T]AGGGTCCAGATGCTG | 63893 |
| rs758968721 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401169 | CCTGCGGGATGTGGG[A/G]CCAAAGGAAAGTCCC | 63893 |
| rs759024133 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400028 | TACACCTGAGTAGCC[A/G]GCAAGGGTCATCAGG | 63893 |
| rs759028925 | snp | A/G | 1.68457e-05 | 0.00290216 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391345 | CTTGGGCACCCCGTT[A/G]GGCAGTGCCTGGGCC | 63893 |
| rs759032712 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | UBE2O | GRCh38.p7 | 17:76396278 | GCTTGTCCTCCTTGC[A/G]CTCTACGTCGGGCAC | 63893 |
| rs759037963 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76402415 | CAGATCAGAAACTGA[A/G]CAACAGAAATAGGCC | 63893 |
| rs759120535 | snp | A/G | 0.000183191 | 0.00956881 | missense | UBE2O | GRCh38.p7 | 17:76391413 | TACGGTTCACCAGCC[A/G]CCAGCCACCAGTGCT | 63893 |
| rs759134620 | snp | C/T | 1.66524e-05 | 0.00288547 | missense | UBE2O | GRCh38.p7 | 17:76401052 | TCTTGGTGCTGAGCA[C/T]GGGCTTGACACCTGA | 63893 |
| rs759139089 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448675 | ATAAACGCTTTGCCT[C/T]CGAAACGAAGGCTGA | 63893 |
| rs759144719 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443358 | CCGGGGCACGATCTC[A/G]GCTCACTGCAACCTC | 63893 |
| rs759152657 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431226 | GAAGTAATAAGTCAA[C/T]AAAAGCCGGCCACGG | 63893 |
| rs759163013 | in-del | -/AT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443283 | AAAAAAAGTTGGGGA[-/AT]ATATATATATATTTT | 63893 |
| rs759221383 | snp | C/T | 3.29875e-05 | 0.00406112 | missense | UBE2O | GRCh38.p7 | 17:76399470 | CCTGGCTTGAAGTCT[C/T]GAGTGATTTTATTCT | 63893 |
| rs759222483 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392216 | TTCCCAGGACACTGT[A/G]CAGATCACGCAGGAA | 63893 |
| rs759313394 | snp | A/G | 8.23662e-05 | 0.00641688 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399559 | ACTCGTGCCGCTGCC[A/G]CTCTGGGAGGAAGTG | 63893 |
| rs759315409 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432617 | GGGGTTAAATCCCAA[C/T]ATAATGCAAAATGGC | 63893 |
| rs759345420 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422122 | GATAAGTAATGGGAC[A/G]TGTGCTAAGTAACCC | 63893 |
| rs759348756 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453370 | AATCCACTAAGAAGG[A/G]GCGAGACCAGTGAGG | 63893 |
| rs759375922 | snp | C/T | 4.94214e-05 | 0.00497074 | missense | UBE2O | GRCh38.p7 | 17:76398319 | ACGATGTCAGTTGTA[C/T]GGAACCTAAAGTCAG | 63893 |
| rs759381468 | snp | A/G | 1.76739e-05 | 0.00297265 | intron-variant | UBE2O | GRCh38.p7 | 17:76399924 | ACAGGCGCTTCACCT[A/G]CAAGGGCGGAGCAGA | 63893 |
| rs759459526 | snp | A/C | 0.000951701 | 0.0217932 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76453018 | ACGGCCCGGAGGCCG[A/C]GTCCGAGGCGGGCGC | 63893 |
| rs759467117 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant | UBE2O | GRCh38.p7 | 17:76398395 | TCAGCTGTGGCACAG[A/G]ACAGGTTGTCATGAG | 63893 |
| rs759468779 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393118 | AAAAAATTAGCTGGG[C/T]ATGGTGGTGCATACC | 63893 |
| rs759486941 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442623 | CATGAGAGGAAGGGA[A/C]CGGCACAATTGAGTT | 63893 |
| rs759497833 | snp | C/T | 6.63064e-05 | 0.0057575 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452804 | CGCAGGGGGCTGGCC[C/T]GGCCCTCCTCGTGGC | 63893 |
| rs759558089 | in-del | -/AA | 1.97143e-05 | 0.00313955 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452715 | CCGCCCAGCCCCCGC[-/AA]CCGCCGCACCTTGGT | 63893 |
| rs759559863 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427782 | CAATCCAGAGTGTGG[A/G]GCAATGATCAGCTCC | 63893 |
| rs759586977 | snp | A/G | 0.000214732 | 0.0103595 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391066 | GGGGAAGCCGATGTC[A/G]GGGTAGCCACTCTTC | 63893 |
| rs759617825 | snp | C/T | 7.38598e-05 | 0.00607655 | intron-variant | UBE2O | GRCh38.p7 | 17:76400579 | GTGGGACACGCCAGT[C/T]AGGGCAGGCTCTGAC | 63893 |
| rs759625121 | snp | A/G/T | 0.000181303 | 0.00951948 | missense, synonymous-codon | UBE2O | GRCh38.p7 | 17:76398919 | GTCGTTGGAGCGGAT[A/G/T]TTGCATTCCACGGAG | 63893 |
| rs759663154 | snp | A/G | 1.69312e-05 | 0.00290952 | intron-variant | UBE2O | GRCh38.p7 | 17:76398799 | CGGGCCCTCATTGGC[A/G]ACCACCCTGCTGGCT | 63893 |
| rs759786146 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438239 | AGTGGGGAATGATGA[A/G]AAGTTCTGGGGGTGG | 63893 |
| rs759821609 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445128 | TTGCAGGATGCAAAT[A/G]AAGGCCTCTCTTTTT | 63893 |
| rs759829928 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407099 | GCCGACATGTGGAAG[A/G]AGAGATGATGGCAGC | 63893 |
| rs759841188 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434086 | TTATTTCCTAAGAAA[A/G]AAGTCTGTTTTCTTT | 63893 |
| rs759860392 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449744 | GCCACCACGGAGAAA[C/T]CCCGTCTCCACTAAA | 63893 |
| rs759874059 | snp | C/T | 0.000100085 | 0.00707337 | missense | UBE2O | GRCh38.p7 | 17:76396548 | CCTTCTCCATCAGCC[C/T]GGCCATGGGGGCAGC | 63893 |
| rs759876043 | snp | C/T | 1.66344e-05 | 0.0028839 | missense | UBE2O | GRCh38.p7 | 17:76391586 | AAGCCGGCTTCGTTG[C/T]AGTATGGTTCATTTA | 63893 |
| rs759880031 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415276 | CCTGCCAGGAAAGAA[A/C]CCCACGTGCACTGCC | 63893 |
| rs759902938 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | UBE2O | GRCh38.p7 | 17:76395793 | GCAGCGCCATCTCCT[C/T]CCGCACTGTGCTGAA | 63893 |
| rs759925606 | snp | C/G | 3.30033e-05 | 0.00406209 | missense, intron-variant | UBE2O | GRCh38.p7 | 17:76400218 | CAATCTTGGCTGGCT[C/G]TACCTTGGCTGGGAA | 63893 |
| rs759940694 | snp | A/G | 3.2824e-05 | 0.00405104 | intron-variant | UBE2O | GRCh38.p7 | 17:76392118 | GAGAAGAGGTCCTAG[A/G]TAGGGAGGGAGGGAG | 63893 |
| rs759991964 | in-del | -/GA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435404 | AAATATACAGATACA[-/GA]CACACACACACATAC | 63893 |
| rs760013983 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395603 | CCTGTAAAAGGTGGG[C/T]GGGTGAGTGTCCTCG | 63893 |
| rs760024506 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426294 | GCGTGAACCACCATG[A/C]CCAGCCAAAAGAACT | 63893 |
| rs760026376 | in-del | -/TT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76398161 | GAGGACTTTCAGGTC[-/TT]GTCTCCTAGAGCCAC | 63893 |
| rs760063110 | snp | C/T | 1.72249e-05 | 0.00293465 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76390973 | GCACTCCGGCATGCC[C/T]GCCTCTAGCAGGGCA | 63893 |
| rs760107639 | snp | C/T | 6.58989e-05 | 0.00573978 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399598 | GGCAGAGGAGGTCAC[C/T]GAACTGGTGTCGTCC | 63893 |
| rs760151400 | snp | A/G | 1.66763e-05 | 0.00288753 | intron-variant | UBE2O | GRCh38.p7 | 17:76400319 | GGGGAAGAAGTGGGG[A/G]TGAGCTGGGCTGGAC | 63893 |
| rs760169223 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391528 | CATCTCATTGTAACA[A/G]CGACTGTTTTCATAG | 63893 |
| rs760188089 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444332 | AGTGGGAGGATCACT[C/T]GGGGTCAGGAGTTCG | 63893 |
| rs760194329 | snp | A/G | 1.64871e-05 | 0.00287111 | intron-variant | UBE2O | GRCh38.p7 | 17:76398251 | CTTGAATTTGAAGGC[A/G]TACCTCATCCTCCTT | 63893 |
| rs760301499 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442402 | TGGTCTAGTAAGGGG[A/C]CCATACAGCTCCAGC | 63893 |
| rs760335192 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | UBE2O | GRCh38.p7 | 17:76399711 | GCAGCTGCTCTCCTG[C/T]CTCGTGGGGCTCCTC | 63893 |
| rs760354261 | snp | A/G | 0.000198304 | 0.00995555 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76397814 | CTGGGGCAGGATGAT[A/G]GTCTTTGAGTTGTCA | 63893 |
| rs760443570 | snp | A/G | 3.4219e-05 | 0.00413622 | intron-variant | UBE2O | GRCh38.p7 | 17:76405466 | GGCTCAAGTCCCTAA[A/G]GTGGCTGCCCCCAGG | 63893 |
| rs760454245 | snp | A/G | 1.65855e-05 | 0.00287967 | intron-variant, stop-gained | UBE2O | GRCh38.p7 | 17:76397891 | GGCCCACCGATGGCT[A/G]CTGGGCAAAGGGGAC | 63893 |
| rs760492126 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435193 | CAAAGCTCTGACCTG[C/G]CAAATACAGAGCAGT | 63893 |
| rs760567031 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76437063 | CTGAGGCAGGAGAAT[C/T]GCCTGAACCTAGGAG | 63893 |
| rs760589670 | snp | C/T | 1.77874e-05 | 0.00298218 | intron-variant | UBE2O | GRCh38.p7 | 17:76401200 | CGTGAGCGGTGTCTC[C/T]ATGGGTGACCATGCT | 63893 |
| rs760604481 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422086 | CAGGCCTGTGGTGAT[A/G]TTTTTGAGACCTCTA | 63893 |
| rs760629840 | snp | A/C | 3.33189e-05 | 0.00408146 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76401062 | GAGCACGGGCTTGAC[A/C]CCTGACAGCCACTGG | 63893 |
| rs760640210 | snp | C/T | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452576 | TGCAATGACTTTGCA[C/T]GGAGTGTACCCTCCA | 63893 |
| rs760649703 | snp | C/T | 1.65891e-05 | 0.00287998 | missense | UBE2O | GRCh38.p7 | 17:76391439 | GTGCTAAAGTGTTGC[C/T]TGATCTCCTGCTCAA | 63893 |
| rs760657891 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421172 | TCCTCTGACAGGAAA[C/T]GGGAAACTCACAGCT | 63893 |
| rs760677574 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394177 | TCCCGCTTGGCTGCT[C/T]TCAGGATCGCTTGGC | 63893 |
| rs760724773 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399496 | ATTCTTCTTCCTCTT[A/G]TGTTTGCGCTTTAAG | 63893 |
| rs760763080 | snp | C/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451411 | CTCTGAGGGGAAGCA[C/G]GGTCCTGTGTGTGGA | 63893 |
| rs760831407 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443840 | AGCTGCACATCTATG[A/G]GTAAGAGGAAGAAGA | 63893 |
| rs760836131 | snp | C/T | 1.66449e-05 | 0.00288482 | intron-variant | UBE2O | GRCh38.p7 | 17:76391853 | TTCTGTTCCCCAGGC[C/T]CCTATCCACCAGTGG | 63893 |
| rs760858402 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412957 | AGGTTGCAGTGAGCC[A/G]AGATTGCGCCATTGC | 63893 |
| rs760866715 | snp | C/T | 3.29766e-05 | 0.00406045 | missense | UBE2O | GRCh38.p7 | 17:76399819 | TCTTGGTTTTGGATT[C/T]CCCCTTCTTGTCTGG | 63893 |
| rs760867546 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438687 | AAGTCAAATTGAACA[G/T]CATTAAAATTATCCT | 63893 |
| rs760871948 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415088 | GCTCCATTTCAGATG[C/T]GACAGGCTGCGGTCC | 63893 |
| rs760947663 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414116 | CCAGCAAAGCACAAA[C/T]GGCCAGGGGGCCTCA | 63893 |
| rs760961057 | snp | A/G | 3.28456e-05 | 0.00405237 | missense | UBE2O | GRCh38.p7 | 17:76405527 | CGGTGGATCGCATGT[A/G]CCGGACCACATCTCG | 63893 |
| rs761001081 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430654 | TATTGATTTTGCCAC[A/G]GCCATGCTTGTAGAT | 63893 |
| rs761029173 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426131 | CTTCAGCCTCCTGAG[G/T]AGCTGGGACTACAGA | 63893 |
| rs761037369 | snp | C/T | 1.64942e-05 | 0.00287173 | intron-variant | UBE2O | GRCh38.p7 | 17:76402722 | CCAAGGAGGCAGGGG[C/T]AGTGAGACACAGCAG | 63893 |
| rs761042286 | snp | A/C | 1.6748e-05 | 0.00289374 | intron-variant | UBE2O | GRCh38.p7 | 17:76400334 | GTGAGCTGGGCTGGA[A/C]TCCTGGGAGGCCAGC | 63893 |
| rs761111343 | in-del | -/GGGG | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451775 | GGGGTGTGAGATACA[-/GGGG]GGTGTGTGTGTGTGT | 63893 |
| rs761119087 | snp | A/G | 3.31763e-05 | 0.00407272 | intron-variant | UBE2O | GRCh38.p7 | 17:76395906 | TCATGGAGAGGCCCT[A/G]GAGCTCCATCTGCCA | 63893 |
| rs761128133 | snp | A/G | 1.67489e-05 | 0.00289381 | intron-variant | UBE2O | GRCh38.p7 | 17:76398824 | CTGGCTGCCCTTCCA[A/G]AGCTGGCACTACCTC | 63893 |
| rs761132235 | snp | A/G | 1.74763e-05 | 0.00295598 | intron-variant | UBE2O | GRCh38.p7 | 17:76400429 | GGTTGCTGGCAGTAA[A/G]GGCATGCTTACCTGC | 63893 |
| rs761153937 | in-del | -/G | 6.64005e-05 | 0.00576158 | frameshift-variant | UBE2O | GRCh38.p7 | 17:76391461 | CTGCTCAAAGACCTC[-/G]GGGGGGCCGCCGCAC | 63893 |
| rs761205208 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438132 | TTGGTAGGTGACCAC[A/G]TGTCTACATCCACTG | 63893 |
| rs761234552 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393392 | CTTCAGTCTCCTCAC[A/G]CCCGGCTAATTTTTT | 63893 |
| rs761235210 | snp | A/G | 1.66158e-05 | 0.0028823 | intron-variant | UBE2O | GRCh38.p7 | 17:76397903 | GCTGCTGGGCAAAGG[A/G]GACAAAGTCAGGGGG | 63893 |
| rs761279677 | snp | G/T | 6.61682e-05 | 0.0057515 | missense | UBE2O | GRCh38.p7 | 17:76391178 | GAAGTCTGGTCTGTG[G/T]GGTCCCTGCTAGCTG | 63893 |
| rs761310196 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448486 | GCAAAGCCAATTCCC[A/G]AGGGACCTGTCATCA | 63893 |
| rs761355341 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76451205 | GAAAAACATTCTTAA[A/G]AACTCACAGAAAGAC | 63893 |
| rs761364365 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76396072 | CAGATCTGGTGACAC[A/C]AACAGGAGCCCCGAG | 63893 |
| rs761385678 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428303 | TTTTGAAACTTATGA[C/T]TGTCCATTCTGAAAT | 63893 |
| rs761420009 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408312 | CTACCTGGCAGACAG[C/T]TCTCCAAGCGTTTCA | 63893 |
| rs761431551 | snp | A/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452414 | CGCCCCAGAACCTGA[A/G]TCCCCACGGGAGTCG | 63893 |
| rs761439412 | snp | A/G | 4.83664e-05 | 0.00491741 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452781 | ACTGGACGCGCACGT[A/G]GCCGCGGCGCAGGGG | 63893 |
| rs761463182 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420220 | CACTCAGCAGTGCTA[C/T]TTTTAAAAATGCAAA | 63893 |
| rs761477535 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436117 | CCAGGCATGGTGGTG[G/T]GCACCTGTAATCCCA | 63893 |
| rs761480042 | snp | A/G | 1.64944e-05 | 0.00287175 | intron-variant | UBE2O | GRCh38.p7 | 17:76398239 | AGCCATCCAGAACTT[A/G]AATTTGAAGGCGTAC | 63893 |
| rs761502532 | snp | A/G | 1.6855e-05 | 0.00290297 | intron-variant | UBE2O | GRCh38.p7 | 17:76405590 | GTAAAAGAAAATACA[A/G]GTGTGAGAGAATGGA | 63893 |
| rs761513501 | snp | A/G | 0.00031678 | 0.0125813 | intron-variant | UBE2O | GRCh38.p7 | 17:76395963 | ACAGACTTCCCACTC[A/G]CCGCTGCTGGCCTCA | 63893 |
| rs761531315 | in-del | -/CA | 1.83011e-05 | 0.00302493 | intron-variant | UBE2O | GRCh38.p7 | 17:76395947 | ACAGGTGAGCACACC[-/CA]CAGACTTCCCACTCG | 63893 |
| rs761546526 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397377 | GAGGGAAGGAGAGCC[C/T]GTGTAGCCCTTCTGC | 63893 |
| rs761599555 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409683 | ACAGGCGTGAGCCAC[C/G]GCCCCTGGCAAACAC | 63893 |
| rs761628770 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444956 | CGGTGACCACACACA[C/G]AGTCCGGTGACCACA | 63893 |
| rs761650345 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419963 | CCCTGGTGCTCCCTG[C/T]CCCTCCTTCATCACC | 63893 |
| rs761686349 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400698 | TCAGAGCAGGCCCCA[A/G]CTGTAACCACGGCCC | 63893 |
| rs761699483 | snp | A/G | 6.59098e-05 | 0.00574026 | missense | UBE2O | GRCh38.p7 | 17:76396418 | TCAGGCTCCACAGTC[A/G]GAGAGGTGGGCGAGC | 63893 |
| rs761706546 | snp | C/T | 0.000100995 | 0.00710543 | missense | UBE2O | GRCh38.p7 | 17:76402102 | CGTCGTAGAGCTTGG[C/T]GCCATCTTCCGTGTT | 63893 |
| rs761778318 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | UBE2O | GRCh38.p7 | 17:76399615 | AACTGGTGTCGTCCG[C/T]GTCATCAGCAGCCTC | 63893 |
| rs761936362 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411864 | AATTTTATTTTTTTT[G/T]TAGAGACTGGGTTTT | 63893 |
| rs761952225 | snp | A/C | 1.69175e-05 | 0.00290834 | intron-variant | UBE2O | GRCh38.p7 | 17:76391877 | CCAGTGGCTCTTCCT[A/C]CTTCTTGGCTGGGGG | 63893 |
| rs761999686 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant | UBE2O | GRCh38.p7 | 17:76398403 | GGCACAGGACAGGTT[A/G]TCATGAGCTAGGGGT | 63893 |
| rs761999992 | snp | C/T | 1.65277e-05 | 0.00287464 | intron-variant | UBE2O | GRCh38.p7 | 17:76402750 | CAGACAACGTTCATG[C/T]CCAGGGCACAGATTC | 63893 |
| rs762018432 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436587 | GCCTCCAGGCCCCTG[C/T]CCTGCACGCTGTCCC | 63893 |
| rs762032734 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417027 | GCCACAGAGTTGCCA[-/C]TCCCCAGCTGTGTGT | 63893 |
| rs762048366 | snp | C/G | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455050 | GAGAATCACTTGAAC[C/G]TGGGGAGTGGAGGTT | 63893 |
| rs762067311 | in-del | -/GCAC | 1.67069e-05 | 0.00289019 | intron-variant | UBE2O | GRCh38.p7 | 17:76398830 | GCCCTTCCAGAGCTG[-/GCAC]TACCTCGCTTATCTA | 63893 |
| rs762087931 | snp | A/G | 5.36351e-05 | 0.00517829 | intron-variant | UBE2O | GRCh38.p7 | 17:76399932 | TTCACCTGCAAGGGC[A/G]GAGCAGAGAGGACAG | 63893 |
| rs762117018 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417266 | TCAGAGCAGGCCAGC[C/T]GAAAGTCAACGACAT | 63893 |
| rs762134574 | in-del | -/CT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449584 | TGTTTAAAAAAGAAA[-/CT]CACACACAAAAATTT | 63893 |
| rs762165530 | in-del | -/CCG | 1.65531e-05 | 0.00287686 | intron-variant | UBE2O | GRCh38.p7 | 17:76391736 | CCCTTGTCCGCACCC[-/CCG]CTTCAGCCCAACTGT | 63893 |
| rs762184050 | snp | G/T | 1.65132e-05 | 0.00287339 | missense, intron-variant | UBE2O | GRCh38.p7 | 17:76400172 | ATAGAGCCCTCCCCC[G/T]GGGCGCAGTTTTTTT | 63893 |
| rs762187180 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429474 | TTCAGCCTGGGAGGC[A/T]GAGGTTGCAGTGAGC | 63893 |
| rs762229952 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405741 | CTCCGACCAGCACCC[-/A]AGACCCACAGGCAGA | 63893 |
| rs762242944 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431500 | GCGACAGGGTGCTCT[C/G]TCTCAAAAAAAAAGT | 63893 |
| rs762255665 | snp | C/T | 1.6549e-05 | 0.0028765 | missense | UBE2O | GRCh38.p7 | 17:76391202 | CTAGCTGAGGCCAGG[C/T]CCTGGGCACCGCCCT | 63893 |
| rs762269115 | snp | A/C | 1.67899e-05 | 0.00289736 | intron-variant | UBE2O | GRCh38.p7 | 17:76399017 | AGGCCAGTCAGCAGG[A/C]CATGCAAACCCCACC | 63893 |
| rs762269152 | snp | G/T | 1.69152e-05 | 0.00290814 | missense | UBE2O | GRCh38.p7 | 17:76396589 | GCCCCCTGGACGGCA[G/T]CTGTGGCTGCCTCTT | 63893 |
| rs762346403 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416061 | CATATGTACATACAC[G/T]TATATACGTATGTGT | 63893 |
| rs762356889 | snp | A/G | 1.66576e-05 | 0.00288592 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396681 | CTCCTCTATCTTGGG[A/G]TGCTCGTCCTCCACC | 63893 |
| rs762357587 | in-del | -/T | 1.86395e-05 | 0.00305277 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390923 | CCCACGGTGATGCTC[-/T]TTTCCTCTGTGCCTG | 63893 |
| rs762363403 | snp | A/G | 2.21051e-05 | 0.00332446 | intron-variant | UBE2O | GRCh38.p7 | 17:76396093 | GAGCCCCGAGAAGGC[A/G]GGGGAAGGCGAAGAC | 63893 |
| rs762364751 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404048 | ATAAAGCTCTTCTAC[A/G]GAGCAGAATGCCAGC | 63893 |
| rs762453593 | snp | A/G | 1.65446e-05 | 0.00287612 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391213 | CAGGCCCTGGGCACC[A/G]CCCTCTGAGTCTGAG | 63893 |
| rs762478509 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402624 | CGTTGGATAGCTTCA[A/G]GATGATCTGGTTCTT | 63893 |
| rs762480668 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446277 | CCAGCGGCAGCTGAC[A/G]CTGATCACGTGCCCA | 63893 |
| rs762484853 | snp | A/C | 3.70556e-05 | 0.00430423 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452681 | GCCTCGGCCCGGCCG[A/C]CGACCCCCTGCCGCC | 63893 |
| rs762529413 | snp | G/T | | | missense | UBE2O | GRCh38.p7 | 17:76399681 | CATCTCTGCCTTCTT[G/T]TAGCAGGAATGGGGG | 63893 |
| rs762538819 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438984 | CCACCTTGTAAACTG[C/T]CGCCAAATCACCCAT | 63893 |
| rs762548653 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433509 | TCTAAAATTAGATAG[C/T]GGTGATGACCGTACA | 63893 |
| rs762570675 | snp | A/G | 5.45717e-05 | 0.0052233 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452793 | CGTAGCCGCGGCGCA[A/G]GGGGCTGGCCCGGCC | 63893 |
| rs762622595 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415444 | CTGCCCTTCCTCATT[C/T]GACCTGTCTGGTCTC | 63893 |
| rs762678062 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408206 | ACCTGCTTCACAAAG[C/G]CTTTCAGTGCCCCCG | 63893 |
| rs762684344 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444388 | GAGACCCTGTTTCTA[-/C]AAAAATATTTTAAAA | 63893 |
| rs762697684 | snp | C/T | 1.68618e-05 | 0.00290356 | missense | UBE2O | GRCh38.p7 | 17:76391341 | TGGCCTTGGGCACCC[C/T]GTTGGGCAGTGCCTG | 63893 |
| rs762702724 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448702 | TGAACTTGAACTGAC[-/A]AGACAGCAGTCCTGC | 63893 |
| rs762746336 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399724 | TGCCTCGTGGGGCTC[C/T]TCTGCACCCTCGTCC | 63893 |
| rs762748026 | snp | C/T | 1.66718e-05 | 0.00288715 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76401023 | CACCTCTTCCACCAC[C/T]ACTCGGAACTTGCTC | 63893 |
| rs762840507 | snp | A/G | 3.29647e-05 | 0.00405971 | missense | UBE2O | GRCh38.p7 | 17:76399797 | GGGCTGGCAGACTCC[A/G]CTTCGCTCTTGGTTT | 63893 |
| rs762842083 | snp | A/G | 8.3273e-05 | 0.0064521 | intron-variant | UBE2O | GRCh38.p7 | 17:76397916 | GGGGACAAAGTCAGG[A/G]GGCCCAGCTCAAGCT | 63893 |
| rs762913987 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432726 | AGATCCAAATGCAGG[G/T]TGTAATAAGCAGACC | 63893 |
| rs762967179 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442095 | AGGCGGGGTTCTTAC[-/A]AGGGGAAATGCAGCC | 63893 |
| rs762989506 | in-del | -/CTTT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409401 | AATGAACACACACTA[-/CTTT]TTTTTTTTTTGAGAC | 63893 |
| rs763008379 | snp | C/T | 0.000284455 | 0.0119225 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390897 | GGAGTGAGCAGGCGG[C/T]GGCTGGCCTCTCCCA | 63893 |
| rs763093268 | snp | A/C/G | 3.50651e-05 | 0.00418707 | missense | UBE2O | GRCh38.p7 | 17:76390965 | TCCTCTGTGCACTCC[A/C/G]GCATGCCTGCCTCTA | 63893 |
| rs763098792 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421204 | CAGTGAGCTCCCTAG[A/G]GCTGAGCCCAACCGT | 63893 |
| rs763104453 | snp | A/G | 1.65002e-05 | 0.00287225 | missense, intron-variant | UBE2O | GRCh38.p7 | 17:76400179 | CCTCCCCCTGGGCGC[A/G]GTTTTTTTCTGGACA | 63893 |
| rs763120879 | in-del | -/CA | 1.64735e-05 | 0.00286993 | frameshift-variant | UBE2O | GRCh38.p7 | 17:76399585 | AAGTGGTGGAGCTGG[-/CA]GAGGAGGTCACCGAA | 63893 |
| rs763126326 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443438 | GGATCACAGGCACCC[A/T]CCACCACGCATGGCT | 63893 |
| rs763138134 | snp | A/C/T | 4.94298e-05 | 0.0049712 | missense | UBE2O | GRCh38.p7 | 17:76402606 | TGAGACTCTACCTGG[A/C/T]GCCGTTGGATAGCTT | 63893 |
| rs763228276 | snp | A/G | 2.54832e-05 | 0.00356945 | intron-variant | UBE2O | GRCh38.p7 | 17:76395994 | GCACTGTGACCACAC[A/G]GGGAAATGGTTTGCC | 63893 |
| rs763229276 | snp | A/G | 1.65195e-05 | 0.00287393 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398556 | AGACTGTACCACACC[A/G]TAGACAGCAGGGTCT | 63893 |
| rs763243551 | snp | A/G | 1.66186e-05 | 0.00288254 | intron-variant | UBE2O | GRCh38.p7 | 17:76391715 | TCACTTTCCTCCACC[A/G]GCCCTCCCTTGTCCG | 63893 |
| rs763297039 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447127 | ACTAAGACTTTCAAC[C/T]GTTTAAAGAAGGGAT | 63893 |
| rs763319538 | snp | C/T | 1.64798e-05 | 0.00287047 | missense | UBE2O | GRCh38.p7 | 17:76396287 | CCTTGCGCTCTACGT[C/T]GGGCACTGCTTCCAT | 63893 |
| rs763319665 | snp | C/T | 4.94181e-05 | 0.00497057 | intron-variant | UBE2O | GRCh38.p7 | 17:76398795 | AACCCGGGCCCTCAT[C/T]GGCGACCACCCTGCT | 63893 |
| rs763323125 | snp | A/G | 5.43601e-05 | 0.00521317 | intron-variant | UBE2O | GRCh38.p7 | 17:76396828 | GTACAAGTGCTGGGG[A/G]CAGAAGGGAAGTGCC | 63893 |
| rs763342762 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439983 | AGTGCTCACTAAACA[A/C]ATCTCTCCTAGCACC | 63893 |
| rs763443332 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411460 | TGAACACTAAATGGG[A/C]TCCCAGTTCAAAAAG | 63893 |
| rs763447974 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449959 | AAGTTTCTCAAAACC[A/T]TCACTACTGTAGTCC | 63893 |
| rs763449920 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420104 | AGCAGTGGCCCCCTT[C/T]GCACCACACTCCCCC | 63893 |
| rs763508877 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415495 | CCTGGACCAATTGGA[A/G]CCATGCTGCCATTCA | 63893 |
| rs763559987 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428088 | GATTGTAATGGGAGC[A/G]GTTCTAACTTTAGCT | 63893 |
| rs763580143 | snp | C/T | 3.31246e-05 | 0.00406955 | missense | UBE2O | GRCh38.p7 | 17:76405267 | TTGGTGCCGATGAGC[C/T]TGACGGCACAGTCGA | 63893 |
| rs763610862 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399610 | CACCGAACTGGTGTC[A/G]TCCGTGTCATCAGCA | 63893 |
| rs763638453 | snp | A/C | 1.65474e-05 | 0.00287636 | intron-variant | UBE2O | GRCh38.p7 | 17:76397748 | CCTGTGGCCCCCGGC[A/C]CAAGTTGCCATAGTC | 63893 |
| rs763659418 | snp | C/G | 0.00509941 | 0.0502364 | intron-variant | UBE2O | GRCh38.p7 | 17:76405474 | TCCCTAAGGTGGCTG[C/G]CCCCAGGCCCGGGGC | 63893 |
| rs763675176 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419895 | AGAAAGAAGCATGCC[A/G]GCAGAAGGAGGCATG | 63893 |
| rs763716043 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444378 | ATACCATGGTGAGAC[A/C]CTGTTTCTACAAAAA | 63893 |
| rs763716871 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394426 | CTAGGCCCCGTCCAC[A/G]AACAGAGGAGTGGGA | 63893 |
| rs763741898 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76396024 | CCTGGGGCAGTAGCT[A/G]GGGTCTGGCGAGGGG | 63893 |
| rs763762484 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438995 | ACTGCCGCCAAATCA[C/G]CCATTGTAAACTCTG | 63893 |
| rs763789963 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431929 | GCTGTGATCTAACCA[C/T]GACAGTCAGAACTGA | 63893 |
| rs763827091 | snp | G/T | 1.65187e-05 | 0.00287386 | missense | UBE2O | GRCh38.p7 | 17:76395852 | TCAATTTTCTTAAAA[G/T]AATGATTTGCTAGAG | 63893 |
| rs763935618 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | UBE2O | GRCh38.p7 | 17:76399504 | TCCTCTTGTGTTTGC[A/G]CTTTAAGTTCTTGAT | 63893 |
| rs763949024 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443622 | TTAAGTCCACAGACT[G/T]GGGGATGGGAAGGGC | 63893 |
| rs763985993 | in-del | -/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397130 | TAGGGGACCTTGGCA[-/G]GCCCAGTCCCACACC | 63893 |
| rs764090054 | snp | A/G | 1.77168e-05 | 0.00297626 | intron-variant | UBE2O | GRCh38.p7 | 17:76401203 | GAGCGGTGTCTCCAT[A/G]GGTGACCATGCTCTC | 63893 |
| rs764104315 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432888 | ATCACAATGCAATAC[C/T]CATGCATGCCCACTA | 63893 |
| rs764132543 | snp | A/T | 1.64773e-05 | 0.00287026 | missense | UBE2O | GRCh38.p7 | 17:76399743 | GCACCCTCGTCCTGC[A/T]TCTCCACTGGACTGG | 63893 |
| rs764199321 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403694 | AGCCAAGTAGCAATT[A/G]GCACACCTAGCATCC | 63893 |
| rs764201464 | in-del | -/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409584 | ATTTCTAGTAGAGAT[-/G]GGAGTTTCACCATGT | 63893 |
| rs764260315 | in-del | -/ACACACACA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435408 | TATACAGATACACAC[-/ACACACACA]TACACACACACACAC | 63893 |
| rs764310794 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421211 | CTCCCTAGAGCTGAG[A/C]CCAACCGTAGGGAAA | 63893 |
| rs764315531 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446220 | TGAAAACCCACATGT[C/T]ACAGAAAACCACCCT | 63893 |
| rs764319583 | snp | A/T | 1.64757e-05 | 0.00287012 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402616 | CCTGGCGCCGTTGGA[A/T]AGCTTCAGGATGATC | 63893 |
| rs764375159 | snp | A/C | 1.64933e-05 | 0.00287165 | missense | UBE2O | GRCh38.p7 | 17:76399826 | TTTGGATTCCCCCTT[A/C]TTGTCTGGGTCTTCC | 63893 |
| rs764394968 | snp | C/T | 3.353e-05 | 0.00409437 | intron-variant | UBE2O | GRCh38.p7 | 17:76400336 | GAGCTGGGCTGGACT[C/T]CTGGGAGGCCAGCAG | 63893 |
| rs764425464 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428127 | CATGTCACTGAAACA[C/G]GAAATCCACCCCATT | 63893 |
| rs764459575 | snp | C/T | 3.29511e-05 | 0.00405887 | missense | UBE2O | GRCh38.p7 | 17:76402645 | TCTGGTTCTTCAAGT[C/T]GTAGACCTTCCCCAG | 63893 |
| rs764480697 | snp | A/G | 1.67368e-05 | 0.00289277 | intron-variant | UBE2O | GRCh38.p7 | 17:76398826 | GGCTGCCCTTCCAGA[A/G]CTGGCACTACCTCGC | 63893 |
| rs764482702 | snp | A/G | 1.74583e-05 | 0.00295446 | intron-variant | UBE2O | GRCh38.p7 | 17:76400430 | GTTGCTGGCAGTAAG[A/G]GCATGCTTACCTGCC | 63893 |
| rs764502270 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414680 | AGCCTGCCCGAGGGA[C/T]AGAGAAAGGGGACTG | 63893 |
| rs764510546 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415672 | CAGCTGGGTGTGGTG[A/G]TGCGCACCTGTAATC | 63893 |
| rs764546792 | snp | G/T | 1.6498e-05 | 0.00287206 | missense | UBE2O | GRCh38.p7 | 17:76391086 | AGCCACTCTTCTCAG[G/T]TAAGAAGCTCCGGTA | 63893 |
| rs764552754 | in-del | -/ACATA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435414 | GATACACACACACAC[-/ACATA]CACACACACACACAC | 63893 |
| rs764570685 | snp | C/T | 9.89218e-05 | 0.00703215 | missense | UBE2O | GRCh38.p7 | 17:76398930 | GGATGTTGCATTCCA[C/T]GGAGCCATCCTGCCA | 63893 |
| rs764649091 | snp | C/T | 9.8943e-05 | 0.0070329 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396462 | CTCCACAGTCATGTT[C/T]TTGAGGCTCTCCAGG | 63893 |
| rs764750146 | snp | A/G | 4.98575e-05 | 0.00499262 | intron-variant | UBE2O | GRCh38.p7 | 17:76397904 | CTGCTGGGCAAAGGG[A/G]ACAAAGTCAGGGGGC | 63893 |
| rs764778038 | snp | A/G | 2.39593e-05 | 0.00346108 | intron-variant | UBE2O | GRCh38.p7 | 17:76396085 | ACAAACAGGAGCCCC[A/G]AGAAGGCGGGGGAAG | 63893 |
| rs764802300 | snp | C/G | 3.42841e-05 | 0.00414016 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400458 | GCCTAGGTTTTCCTG[C/G]GTGATGACAGAGGGT | 63893 |
| rs764804416 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405499 | CGGGGCTGGGGTGGG[A/G]ACGCAGGACTCACGG | 63893 |
| rs764821937 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393586 | AAACACCTGCTCCAA[A/C]CCTTATCCCCAACAA | 63893 |
| rs764837828 | snp | G/T | 2.13067e-05 | 0.00326388 | intron-variant | UBE2O | GRCh38.p7 | 17:76395966 | GACTTCCCACTCGCC[G/T]CTGCTGGCCTCAGCA | 63893 |
| rs764883849 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431603 | CATTTTGATGGACTC[C/T]CCTCATGTTGCTATT | 63893 |
| rs764893079 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407151 | GAGTCACCAAGGCAG[A/C]GGACCGCAGGTGGCA | 63893 |
| rs764944129 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417816 | GCATGGATGCATCAG[C/T]GTCCGCGAAGAGACG | 63893 |
| rs764961456 | snp | A/G | 3.30355e-05 | 0.00406407 | missense | UBE2O | GRCh38.p7 | 17:76391136 | GGTTTCACACTGGGT[A/G]GCACCGATGCGTCTG | 63893 |
| rs765017989 | snp | C/T | 4.96175e-05 | 0.00498059 | missense | UBE2O | GRCh38.p7 | 17:76391469 | AAGACCTCGGGGGGC[C/T]GCCGCACCAGCTGGG | 63893 |
| rs765050393 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434467 | ACTGTAAAGGACACG[C/T]CAATAGTCCTGCCAT | 63893 |
| rs765055564 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441894 | CAGGCCCCGCCCCCA[A/G]GGGTCTTGGTGCAGG | 63893 |
| rs765061414 | snp | A/C | 1.64784e-05 | 0.00287035 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396420 | AGGCTCCACAGTCGG[A/C]GAGGTGGGCGAGCCC | 63893 |
| rs765064091 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399616 | ACTGGTGTCGTCCGT[A/G]TCATCAGCAGCCTCA | 63893 |
| rs765083048 | snp | A/G | 1.65282e-05 | 0.00287469 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76397826 | GATGGTCTTTGAGTT[A/G]TCAGCCCACACCACC | 63893 |
| rs765106288 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436262 | AAAAATTAATTAATT[A/T]ATTAATTAATTAACA | 63893 |
| rs765152145 | snp | G/T | 1.64779e-05 | 0.00287031 | missense | UBE2O | GRCh38.p7 | 17:76399719 | TCTCCTGCCTCGTGG[G/T]GCTCCTCTGCACCCT | 63893 |
| rs765225575 | snp | A/G | 8.23879e-05 | 0.00641772 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398481 | ACACACCTCCACGTC[A/G]TCCCCACTCGGCCTC | 63893 |
| rs765231628 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403205 | AGGAGAAGAAGGAAG[-/C]AGGAGTCTGAGGTGT | 63893 |
| rs765284278 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442624 | ATGAGAGGAAGGGAA[C/T]GGCACAATTGAGTTG | 63893 |
| rs765290648 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430127 | TTCCGCAGGTACCAA[C/T]ATTTCAGCCTCTGCT | 63893 |
| rs765291512 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443939 | TAAGAGGGCATGGTC[A/G]GCCAGGCGCGGTAGC | 63893 |
| rs765294001 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445137 | GCAAATGAAGGCCTC[C/T]CTTTTTAAGGGTGCC | 63893 |
| rs765318152 | snp | A/G | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390387 | CATGTATAGCCGGGA[A/G]TCAGTGACAGCAGCT | 63893 |
| rs765371406 | in-del | -/G | 0.000214678 | 0.0103582 | frameshift-variant | UBE2O | GRCh38.p7 | 17:76392007 | AGAGGTAGCAGAAGT[-/G]GGGGGGGCACGGCTG | 63893 |
| rs765388627 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415485 | CCTTGCTACACCTGG[A/G]CCAATTGGAACCATG | 63893 |
| rs765450180 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423899 | TCCAGGTTGGGTTCT[-/TTTTTTTTTTTTTT]TTTTTTTTGAGACGG | 63893 |
| rs765455651 | snp | A/G | 1.78777e-05 | 0.00298974 | intron-variant | UBE2O | GRCh38.p7 | 17:76399933 | TCACCTGCAAGGGCG[A/G]AGCAGAGAGGACAGG | 63893 |
| rs765458710 | snp | C/T | 0.000110284 | 0.00742495 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452828 | TCGTGGCCCGCGCCC[C/T]CGGCCTCGGAGCACC | 63893 |
| rs765492413 | snp | A/T | 3.29484e-05 | 0.00405871 | intron-variant | UBE2O | GRCh38.p7 | 17:76398407 | CAGGACAGGTTGTCA[A/T]GAGCTAGGGGTCCTA | 63893 |
| rs765506877 | in-del | -/T | 1.68641e-05 | 0.00290375 | intron-variant | UBE2O | GRCh38.p7 | 17:76399439 | GGAGGGGCACAACTC[-/T]TGAGTTTACCTGTCC | 63893 |
| rs765628982 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408142 | CTGTGAGCCACTCCA[C/G]TGAACAGTTACTTCC | 63893 |
| rs765630769 | snp | C/T | 1.69083e-05 | 0.00290755 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396591 | CCCCTGGACGGCAGC[C/T]GTGGCTGCCTCTTCA | 63893 |
| rs765676711 | snp | A/T | 1.6808e-05 | 0.00289892 | intron-variant | UBE2O | GRCh38.p7 | 17:76399023 | GTCAGCAGGCCATGC[A/T]AACCCCACCCCCTCC | 63893 |
| rs765680772 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438271 | TGGTGGGGATGGTTG[C/T]ACAACAATGGGAATG | 63893 |
| rs765722923 | snp | A/G | 3.30033e-05 | 0.00406209 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391778 | GGAGATGAGCACCTG[A/G]AGAAGGCTGGACTTG | 63893 |
| rs765802909 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414584 | AACGCAGACTCTCAG[A/G]CTGGGCAATACAGTG | 63893 |
| rs765804023 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429887 | GCCCAAGGTACCTCA[A/G]TCTGGTGCATAAGCC | 63893 |
| rs765844618 | snp | A/G | 2.12995e-05 | 0.00326332 | intron-variant | UBE2O | GRCh38.p7 | 17:76396097 | CCCGAGAAGGCGGGG[A/G]AAGGCGAAGACCAGG | 63893 |
| rs765845761 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402634 | CTTCAGGATGATCTG[A/G]TTCTTCAAGTCGTAG | 63893 |
| rs765934813 | snp | A/G | 1.65685e-05 | 0.00287819 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391234 | TGAGTCTGAGCCCTG[A/G]GAGGCCTCTCCTGGG | 63893 |
| rs765943714 | snp | C/T | 5.90441e-05 | 0.0054331 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452798 | CCGCGGCGCAGGGGG[C/T]TGGCCCGGCCCTCCT | 63893 |
| rs765945405 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | UBE2O | GRCh38.p7 | 17:76400477 | ATGACAGAGGGTGGG[A/G]GGCTGACGCTGTCCG | 63893 |
| rs766018322 | snp | C/T | | | missense | UBE2O | GRCh38.p7 | 17:76399744 | CACCCTCGTCCTGCA[C/T]CTCCACTGGACTGGC | 63893 |
| rs766034432 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441865 | TAATAGGCCTGGCAT[A/G]GCCACTGCAACTCCA | 63893 |
| rs766070466 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431143 | TCCAGCCAAAAAAGA[A/G]GCAACCGGAGGTTTT | 63893 |
| rs766074056 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408615 | GAAAAACTCTCTTCA[C/T]TTCTGAGGCAAGTGG | 63893 |
| rs766109585 | snp | A/C | 1.64768e-05 | 0.00287021 | missense | UBE2O | GRCh38.p7 | 17:76399732 | GGGGCTCCTCTGCAC[A/C]CTCGTCCTGCATCTC | 63893 |
| rs766131101 | snp | C/T | 6.59294e-05 | 0.00574111 | missense | UBE2O | GRCh38.p7 | 17:76399801 | TGGCAGACTCCGCTT[C/T]GCTCTTGGTTTTGGA | 63893 |
| rs766152419 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421190 | GAAACTCACAGCTAC[A/T]GTGAGCTCCCTAGAG | 63893 |
| rs766217332 | snp | A/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451512 | TAGGAAATGGATCAT[A/G]TGCTCTTCTCTGGAG | 63893 |
| rs766291482 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397570 | AGGTTTGTGAAAGTC[C/T]ACATGCACCCAGAGA | 63893 |
| rs766312385 | snp | C/T | 1.67125e-05 | 0.00289067 | missense | UBE2O | GRCh38.p7 | 17:76391400 | AGCCAGGACTCGATA[C/T]GGTTCACCAGCCGCC | 63893 |
| rs766348632 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409921 | AGAAAAACTAGGCCA[C/T]ATGGGGGCCAGCAGA | 63893 |
| rs766416215 | in-del | -/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408888 | AGGGGATCTGGGGTC[-/G]GGGGTGAAGAGATTT | 63893 |
| rs766421534 | in-del | -/GAGGTCACC | 1.64741e-05 | 0.00286998 | cds-indel | UBE2O | GRCh38.p7 | 17:76399590 | GTGGAGCTGGCAGAG[-/GAGGTCACC]GAACTGGTGTCGTCC | 63893 |
| rs766428225 | snp | A/C | 3.21704e-05 | 0.00401051 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452686 | GGCCCGGCCGCCGAC[A/C]CCCTGCCGCCCGCGC | 63893 |
| rs766450242 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440713 | GGAAAACTACAGCCT[A/G]CAGGTCATGTCCAGC | 63893 |
| rs766520975 | snp | A/C | 1.64757e-05 | 0.00287012 | intron-variant | UBE2O | GRCh38.p7 | 17:76398424 | AGCTAGGGGTCCTAC[A/C]CCCAACCCCAGAGCC | 63893 |
| rs766611334 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443861 | AGGAAGAAGACAAAA[G/T]GCAAAAAAGAGAAAC | 63893 |
| rs766630941 | snp | A/G | | | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399655 | GTCCTGCTCTGCCGA[A/G]TGCAGCCTGTCATCT | 63893 |
| rs766686733 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432256 | CCCGTCAAACTGCTA[C/T]GGAAAGGACTCAGTT | 63893 |
| rs766704396 | snp | A/G | 1.66651e-05 | 0.00288657 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399451 | ACTCTGAGTTTACCT[A/G]TCCCCTGGCTTGAAG | 63893 |
| rs766713167 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414161 | GGGAGGGAGAACCTC[C/T]GGAAATGGCTGGAAG | 63893 |
| rs766762779 | snp | A/C | 1.64735e-05 | 0.00286993 | missense | UBE2O | GRCh38.p7 | 17:76391916 | TATACTCACCTTTCC[A/C]ATCCAGGTGCCCAGG | 63893 |
| rs766794512 | snp | C/T | 1.81424e-05 | 0.00301179 | intron-variant | UBE2O | GRCh38.p7 | 17:76396829 | TACAAGTGCTGGGGG[C/T]AGAAGGGAAGTGCCA | 63893 |
| rs766813875 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394280 | ACTCAGATTCAGAGT[A/C]TAGCATAGTGCTTGG | 63893 |
| rs766817179 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438195 | ACTTAATGGTTTGAG[A/G]AGTTATTATTTAATT | 63893 |
| rs766824224 | in-del | -/ACAC | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389507 | CTTGCTAATGAGCCA[-/ACAC]AAAAAAAAAAAAAAA | 63893 |
| rs766824855 | snp | G/T | 1.74336e-05 | 0.00295237 | intron-variant | UBE2O | GRCh38.p7 | 17:76405187 | CAGAAAGGATGATGA[G/T]AAGACAGGGCCGGCT | 63893 |
| rs766846744 | snp | A/G | 8.27695e-05 | 0.00643256 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76392030 | CACGGCTGGGTAGAT[A/G]TTGGGGAGCTGGATG | 63893 |
| rs766910974 | snp | C/G | 1.79383e-05 | 0.0029948 | intron-variant | UBE2O | GRCh38.p7 | 17:76399938 | TGCAAGGGCGGAGCA[C/G]AGAGGACAGGGCTGT | 63893 |
| rs766915521 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409699 | GCCCCTGGCAAACAC[A/C]CACCACTTTGCACAC | 63893 |
| rs766934616 | in-del | -/TACACACACACACA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435401 | GTTTAAATATACAGA[-/TACACACACACACA]CATACACACACACAC | 63893 |
| rs767016683 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422630 | GTGTGGCCACCACAG[C/G]GAACAGCCATGGCTC | 63893 |
| rs767038815 | snp | A/G | 1.66012e-05 | 0.00288103 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391429 | CCAGCCACCAGTGCT[A/G]AAGTGTTGCCTGATC | 63893 |
| rs767084001 | snp | C/T | 3.43424e-05 | 0.00414367 | intron-variant | UBE2O | GRCh38.p7 | 17:76399040 | ACCCCACCCCCTCCG[C/T]GGAAAGGGCAGAGAG | 63893 |
| rs767167301 | snp | C/G | 1.7303e-05 | 0.00294129 | intron-variant | UBE2O | GRCh38.p7 | 17:76405194 | GATGATGAGAAGACA[C/G]GGCCGGCTCACCCAG | 63893 |
| rs767169303 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428557 | TGTGCTTTAAGGCTT[A/T]CTCCTACCTGAATCA | 63893 |
| rs767201413 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429541 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 63893 |
| rs767213487 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441640 | CATCAATGTCACTGG[C/G]AGTTTGTTAGACACG | 63893 |
| rs767225501 | in-del | -/TGTGTTTTTGAC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446897 | TCTCTAGAAATGCAA[-/TGTGTTTTTGAC]TGTGTTTTTGACAGT | 63893 |
| rs767246684 | snp | C/G | 3.29473e-05 | 0.00405864 | intron-variant | UBE2O | GRCh38.p7 | 17:76398399 | CTGTGGCACAGGACA[C/G]GTTGTCATGAGCTAG | 63893 |
| rs767254968 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432971 | ACTGGAACCCACCAA[C/T]ATTGCTGGTGGGTAT | 63893 |
| rs767261917 | snp | C/T | 1.853e-05 | 0.00304379 | intron-variant | UBE2O | GRCh38.p7 | 17:76396856 | GCCAGGGTAAGCAGA[C/T]AGGAAGTCACCTCCC | 63893 |
| rs767277165 | snp | A/G | 6.68025e-05 | 0.005779 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452806 | CAGGGGGCTGGCCCG[A/G]CCCTCCTCGTGGCCC | 63893 |
| rs767295970 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433899 | TAGCCAGGCGTGGCG[A/G]TGCGCGCCTACAGGC | 63893 |
| rs767331166 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392293 | GGACAAATCTCTCTC[C/T]GCAGAACAGCCTGGA | 63893 |
| rs767347470 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444994 | TCCGCTGAATCTGCC[A/G]GTCAAGGTATCTATC | 63893 |
| rs767365100 | snp | C/T | 2.71271e-05 | 0.00368277 | intron-variant | UBE2O | GRCh38.p7 | 17:76400584 | ACACGCCAGTCAGGG[C/T]AGGCTCTGACAGCAC | 63893 |
| rs767416771 | snp | C/G | 1.66394e-05 | 0.00288434 | missense | UBE2O | GRCh38.p7 | 17:76391269 | GCCCTCCATCCTCAG[C/G]TTCTTGTTGGCCGGA | 63893 |
| rs767422684 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417697 | ACCACGAAGGGCCTT[C/T]GACTACAGGAGGAAA | 63893 |
| rs767432939 | in-del | -/G | 0.00013375 | 0.00817663 | intron-variant | UBE2O | GRCh38.p7 | 17:76400330 | GGGGTGAGCTGGGCT[-/G]GGACTCCTGGGAGGC | 63893 |
| rs767447483 | in-del | -/GGC | 0.000235322 | 0.0108446 | upstream-variant-2KB, utr-variant-5-prime | AANAT, UBE2O | GRCh38.p7 | 17:76453162 | TCTGCGCGAGTCTCG[-/GGC]GGCGGCGGCGGCGAC | 63893 |
| rs767503861 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420015 | AGAAGCATGACATAA[C/T]CTTGGGGCAGCAGAA | 63893 |
| rs767506881 | snp | G/T | 1.68326e-05 | 0.00290104 | missense | UBE2O | GRCh38.p7 | 17:76391355 | CCGTTGGGCAGTGCC[G/T]GGGCCTTCTCCAGCA | 63893 |
| rs767520658 | snp | C/G | 1.64822e-05 | 0.00287068 | missense | UBE2O | GRCh38.p7 | 17:76396430 | GTCGGAGAGGTGGGC[C/G]AGCCCGTCAGCAGCT | 63893 |
| rs767525492 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408395 | CTCATTTTGCAGATA[C/T]GCAAACTGAGACCAA | 63893 |
| rs767549169 | snp | C/T | 1.71361e-05 | 0.00292707 | intron-variant | UBE2O | GRCh38.p7 | 17:76402051 | GGGTGCTGGCCTGGA[C/T]GGAGCACACTACCGA | 63893 |
| rs767550535 | snp | C/G | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390044 | AGTTTGTAAGCGAAG[C/G]GCTGACAGTAGGCCT | 63893 |
| rs767585725 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412735 | ACCAACTCGGCCGGG[A/C]GCAGTGGCTCAAGCC | 63893 |
| rs767620155 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422484 | CATTCAGCAAACTGA[A/G]TAACCACTGGGTGGG | 63893 |
| rs767645430 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395358 | GAGAGTTTTTTGTAA[-/T]TTTTTTTTTTTTTTT | 63893 |
| rs767645976 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396318 | CTTCTCCTCCTCTAC[A/G]ATGGCCACATTGTCC | 63893 |
| rs767708665 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400027 | ATACACCTGAGTAGC[C/T]GGCAAGGGTCATCAG | 63893 |
| rs767740366 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411762 | GCAAGCAGGGTTCAC[C/T]GCAGCCTCAACCACC | 63893 |
| rs767748264 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436797 | TCTTAGGACAGAGTA[C/T]AAAATGGGGATTAGT | 63893 |
| rs767781518 | snp | A/C | 1.70226e-05 | 0.00291736 | intron-variant | UBE2O | GRCh38.p7 | 17:76402131 | TTCATGGAGCACCTA[A/C]AACAGAGAACAGAGG | 63893 |
| rs767783742 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411922 | TCCTGAGCTCAAGTG[A/T]TCCTCTTGCCTCAGC | 63893 |
| rs767821931 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436104 | TACAAAACATTAGCC[A/G]GGCATGGTGGTGTGC | 63893 |
| rs767824215 | snp | C/T | 1.6674e-05 | 0.00288734 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391594 | TTCGTTGTAGTATGG[C/T]TCATTTACCAGGATC | 63893 |
| rs767830738 | snp | C/T | 1.65559e-05 | 0.00287709 | missense | UBE2O | GRCh38.p7 | 17:76405280 | GCTTGACGGCACAGT[C/T]GATGTTGACGTCGAT | 63893 |
| rs767853570 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427357 | TTTAAAAAATAATCC[A/C]TTTTAAGATGTATTC | 63893 |
| rs767866463 | snp | G/T | 0.000370958 | 0.013614 | intron-variant | UBE2O | GRCh38.p7 | 17:76392123 | GAGGTCCTAGGTAGG[G/T]AGGGAGGGAGGGAGG | 63893 |
| rs767914392 | snp | A/C | 3.31263e-05 | 0.00406965 | intron-variant | UBE2O | GRCh38.p7 | 17:76391733 | CCTCCCTTGTCCGCA[A/C]CCCCGCTTCAGCCCA | 63893 |
| rs767922110 | snp | C/T | 1.65015e-05 | 0.00287237 | synonymous-codon, intron-variant | UBE2O | GRCh38.p7 | 17:76400219 | AATCTTGGCTGGCTC[C/T]ACCTTGGCTGGGAAG | 63893 |
| rs767922153 | snp | A/G | 3.60386e-05 | 0.00424476 | intron-variant | UBE2O | GRCh38.p7 | 17:76405346 | AGACATGCAAGTCCC[A/G]TGGTGCAGCAGCCCT | 63893 |
| rs767924848 | snp | C/T | 1.65272e-05 | 0.0028746 | missense | UBE2O | GRCh38.p7 | 17:76397810 | TCACCTGGGGCAGGA[C/T]GATGGTCTTTGAGTT | 63893 |
| rs767945816 | snp | C/T | 3.29571e-05 | 0.00405924 | missense | UBE2O | GRCh38.p7 | 17:76395795 | AGCGCCATCTCCTTC[C/T]GCACTGTGCTGAAGA | 63893 |
| rs767972918 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404131 | AGAGCAATGGCTGGC[A/G]CAGGGGGAACTGTGA | 63893 |
| rs768010169 | snp | A/C | 1.67122e-05 | 0.00289064 | intron-variant | UBE2O | GRCh38.p7 | 17:76400324 | AGAAGTGGGGGTGAG[A/C]TGGGCTGGACTCCTG | 63893 |
| rs768023228 | snp | C/T | 9.97059e-05 | 0.00705996 | missense | UBE2O | GRCh38.p7 | 17:76405240 | TTGCTGTTGACGGGA[C/T]AGATGATGCAGTTGG | 63893 |
| rs768033466 | snp | G/T | 1.70644e-05 | 0.00292094 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76390979 | CGGCATGCCTGCCTC[G/T]AGCAGGGCAGCCCGG | 63893 |
| rs768060087 | snp | A/G | 0.000118655 | 0.00770152 | intron-variant | UBE2O | GRCh38.p7 | 17:76398598 | GACTAGGGAACCAGA[A/G]AAAGGGAAGTGACTA | 63893 |
| rs768069117 | in-del | -/CAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446475 | AACAAAAAAAAAAAC[-/CAAA]CAAACAAAACAGAGA | 63893 |
| rs768104087 | snp | A/G | 0.000117731 | 0.00767149 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402091 | GTGCGGGCAGACGTC[A/G]TAGAGCTTGGCGCCA | 63893 |
| rs768139543 | in-del | -/ACACACACACACAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435404 | TAAATATACAGATAC[-/ACACACACACACAT]ACACACACACACACA | 63893 |
| rs768161855 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447291 | GATTCCTCCACTTAG[A/C]AGTGTGACACTGGGC | 63893 |
| rs768163758 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435621 | TGTGCTGAGCCCTCT[C/T]GAAGGTGATCTCGTG | 63893 |
| rs768171202 | in-del | -/AA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419285 | TAAGACCCTATCTCA[-/AA]AAAAAAAAAAAAAAA | 63893 |
| rs768188098 | snp | C/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389986 | GCCTGTCTCTGGGCA[C/T]TAGGAGAGCCCCCGC | 63893 |
| rs768194210 | snp | A/G | 0.000131865 | 0.00811882 | intron-variant | UBE2O | GRCh38.p7 | 17:76402575 | TATCCTTCCCAAGCC[A/G]ATGGCTCTCTGGTGG | 63893 |
| rs768202099 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410467 | GAATGGCGTGGCCAA[C/T]GCACCCGCAGTGCCA | 63893 |
| rs768340000 | snp | C/T | 3.29598e-05 | 0.00405941 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399772 | GGCAGAGCCATCGGG[C/T]GTCTCCTCAGGGCTG | 63893 |
| rs768349436 | snp | A/T | | | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391135 | TGGTTTCACACTGGG[A/T]GGCACCGATGCGTCT | 63893 |
| rs768374542 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421650 | GATTACAGGCGTGAG[C/T]CACCACGCCCGGCCC | 63893 |
| rs768379519 | in-del | -/GCAGC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423961 | GGCTGTAGTGCTAGT[-/GCAGC]GGCGCGATCTTGGCT | 63893 |
| rs768381098 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76451092 | GTGAGCTGGGCCTAC[C/G]TCCCTGAGTCCTAGG | 63893 |
| rs768477240 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413637 | AAGCTGGAGAATCTC[C/T]ACTCTACTGAATTCT | 63893 |
| rs768501495 | snp | C/G | 1.65141e-05 | 0.00287346 | missense | UBE2O | GRCh38.p7 | 17:76391058 | GGGAAGAGGGGGAAG[C/G]CGATGTCAGGGTAGC | 63893 |
| rs768510736 | snp | A/G | 0.000366154 | 0.0135256 | intron-variant | UBE2O | GRCh38.p7 | 17:76400309 | CACCCTGGTTGGGGA[A/G]GAAGTGGGGGTGAGC | 63893 |
| rs768525670 | snp | C/G | 6.95314e-05 | 0.00589583 | intron-variant | UBE2O | GRCh38.p7 | 17:76402155 | ACAGAGGTTTGGTCT[C/G]CACCAGGGGACACAG | 63893 |
| rs768547100 | snp | C/T | 1.65693e-05 | 0.00287826 | missense | UBE2O | GRCh38.p7 | 17:76396527 | TGGGTGGCCCGTCCT[C/T]GCCAGCCTTCTCCAT | 63893 |
| rs768578670 | in-del | -/ACACAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435412 | CAGATACACACACAC[-/ACACAT]ACACACACACACACA | 63893 |
| rs768585865 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416238 | TGTATATGTGTATAT[A/G]TGTGTGTATATGTAT | 63893 |
| rs768605049 | snp | C/G | 1.69818e-05 | 0.00291387 | intron-variant | UBE2O | GRCh38.p7 | 17:76398788 | AAGCCCCAACCCGGG[C/G]CCTCATTGGCGACCA | 63893 |
| rs768620113 | snp | C/T | 4.94311e-05 | 0.00497123 | missense | UBE2O | GRCh38.p7 | 17:76396413 | GCTTCTCAGGCTCCA[C/T]AGTCGGAGAGGTGGG | 63893 |
| rs768695007 | snp | C/T | 1.64833e-05 | 0.00287078 | missense | UBE2O | GRCh38.p7 | 17:76398879 | GGCAGAACTCGTTGT[C/T]GTCCAGGTGGTGCAC | 63893 |
| rs768706046 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391534 | ATTGTAACAGCGACT[A/G]TTTTCATAGCCTTCC | 63893 |
| rs768724198 | snp | C/T | 3.36389e-05 | 0.00410101 | intron-variant | UBE2O | GRCh38.p7 | 17:76400990 | AAGGACTCCATCTCC[C/T]ACCCTTGGGCCCGGA | 63893 |
| rs768739112 | snp | A/G | 3.40907e-05 | 0.00412846 | missense | UBE2O | GRCh38.p7 | 17:76396775 | GTGCTGCCTTCTACC[A/G]AATCGTAGTCTGACT | 63893 |
| rs768756442 | snp | A/C/T | 5.14446e-05 | 0.0050715 | intron-variant | UBE2O | GRCh38.p7 | 17:76399418 | GGCTTCACGCTGACG[A/C/T]CATTGGGGAGGGGCA | 63893 |
| rs768814148 | snp | A/G | 1.67601e-05 | 0.00289478 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396663 | CAGGGGTGGGATGGG[A/G]GGCTCCTCTATCTTG | 63893 |
| rs768815081 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405174 | GAACCAGAGGGCCCA[G/T]AAAGGATGATGAGAA | 63893 |
| rs768831252 | snp | C/G | 3.81643e-05 | 0.00436815 | missense | UBE2O | GRCh38.p7 | 17:76392003 | TTGGGAGAGGTAGCA[C/G]AAGTGGGGGGGCACG | 63893 |
| rs768853419 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76406217 | CTGATTGTCTCTTTA[A/C]GCACAGCTGGCAGCG | 63893 |
| rs768854306 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447133 | ACTTTCAACTGTTTA[A/T]AGAAGGGATGATTAA | 63893 |
| rs768880181 | in-del | -/CT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420807 | TCGGCCTGCCACACA[-/CT]GTTTATGTCTGTGGC | 63893 |
| rs768910652 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441406 | GCCTTTCTAACACTA[A/C]AGCACTGGCGGATGA | 63893 |
| rs768927371 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398306 | GCCGATGCGGATGAC[A/G]ATGTCAGTTGTACGG | 63893 |
| rs768931132 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397347 | AGCTGGGCTGTGTGG[A/C]TCCAACCAGGAGGCG | 63893 |
| rs768934042 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434794 | TTTTTTTTTTTTTTT[-/A]AAAAAAACAAACAAA | 63893 |
| rs768947981 | snp | A/T | 9.60246e-05 | 0.00692842 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452768 | CCCTCCGGGTACCAC[A/T]GGACGCGCACGTAGC | 63893 |
| rs768954821 | in-del | -/GGG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433626 | TTTTTTTTAAGAGAT[-/GGG]GTCTCGATCGCTTGA | 63893 |
| rs769000142 | snp | A/G | 9.89919e-05 | 0.00703464 | intron-variant | UBE2O | GRCh38.p7 | 17:76398234 | TGAGCAGCCATCCAG[A/G]ACTTGAATTTGAAGG | 63893 |
| rs769018529 | snp | A/G | 0.000124634 | 0.00789312 | intron-variant | UBE2O | GRCh38.p7 | 17:76405580 | AGTTTCAGCTGTAAA[A/G]GAAAATACAGGTGTG | 63893 |
| rs769044596 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430720 | TGTAATACATGGTTT[C/G]ACAATCCTCAGCATG | 63893 |
| rs769165014 | snp | C/T | 2.53553e-05 | 0.00356048 | intron-variant | UBE2O | GRCh38.p7 | 17:76396082 | GACACAAACAGGAGC[C/T]CCGAGAAGGCGGGGG | 63893 |
| rs769223445 | snp | G/T | 1.64931e-05 | 0.00287163 | intron-variant | UBE2O | GRCh38.p7 | 17:76398242 | CATCCAGAACTTGAA[G/T]TTGAAGGCGTACCTC | 63893 |
| rs769232737 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | UBE2O | GRCh38.p7 | 17:76399786 | GCGTCTCCTCAGGGC[C/T]GGCAGACTCCGCTTC | 63893 |
| rs769232944 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | UBE2O | GRCh38.p7 | 17:76402674 | AGCCAGCAGTCATAG[A/G]CAATGTAGTCCCCAT | 63893 |
| rs769252844 | in-del | -/G | 1.64942e-05 | 0.00287173 | intron-variant | UBE2O | GRCh38.p7 | 17:76398239 | AGCCATCCAGAACTT[-/G]AATTTGAAGGCGTAC | 63893 |
| rs769258845 | snp | C/T | 0.00012132 | 0.00778752 | missense | UBE2O | GRCh38.p7 | 17:76396146 | GTGCAAACTCCAGTA[C/T]GGAGAAGACCTCGCC | 63893 |
| rs769320814 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400353 | TGGGAGGCCAGCAGT[A/G]TTCTTAAGCCTCCCC | 63893 |
| rs769320836 | snp | C/T | 1.71973e-05 | 0.0029323 | missense | UBE2O | GRCh38.p7 | 17:76399897 | ACATGATCCGCACAA[C/T]CTGCTTCTTCAACAG | 63893 |
| rs769327841 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413565 | GTTGCATATATAACA[C/T]GTATGTGTCCCGGGT | 63893 |
| rs769344537 | in-del | -/G | 3.29647e-05 | 0.00405971 | intron-variant | UBE2O | GRCh38.p7 | 17:76402578 | CCTTCCCAAGCCGAT[-/G]GCTCTCTGGTGGTGA | 63893 |
| rs769373246 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424028 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 63893 |
| rs769373412 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450051 | GTAACAGTGAGACCC[C/T]ATCCCAAAAATAATA | 63893 |
| rs769411992 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432618 | GGGTTAAATCCCAAC[A/T]TAATGCAAAATGGCT | 63893 |
| rs769456504 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438482 | CCCGGCTCAGCTGTA[C/T]GTGCAAGGCTGTGAA | 63893 |
| rs769470235 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | UBE2O | GRCh38.p7 | 17:76398320 | CGATGTCAGTTGTAC[A/G]GAACCTAAAGTCAGG | 63893 |
| rs769482481 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401709 | GGTGAAACCTCATCT[C/G]CACTAAAAATACAAA | 63893 |
| rs769518373 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419846 | GAGCTGGTGTGAAAG[C/T]GTGGCTCTACCCACG | 63893 |
| rs769525968 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401801 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 63893 |
| rs769572032 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433447 | GCAGGGAAATATGGT[A/G]TGACTCCTAATGGGT | 63893 |
| rs769574272 | snp | C/G | 4.88102e-05 | 0.00493991 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452782 | CTGGACGCGCACGTA[C/G]CCGCGGCGCAGGGGG | 63893 |
| rs769641771 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398913 | GAAGAGGTCGTTGGA[A/G]CGGATGTTGCATTCC | 63893 |
| rs769677752 | snp | C/G | 1.65855e-05 | 0.00287967 | intron-variant | UBE2O | GRCh38.p7 | 17:76391842 | GGCACCATCAATTCT[C/G]TTCCCCAGGCCCCTA | 63893 |
| rs769686069 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425874 | CCTGTCTCTCTAACT[C/T]AGACTTTCCTCTGCC | 63893 |
| rs769730793 | snp | C/T | 1.65924e-05 | 0.00288027 | missense | UBE2O | GRCh38.p7 | 17:76396533 | GCCCGTCCTTGCCAG[C/T]CTTCTCCATCAGCCC | 63893 |
| rs769763885 | snp | C/T | | | missense | UBE2O | GRCh38.p7 | 17:76399617 | CTGGTGTCGTCCGTG[C/T]CATCAGCAGCCTCAT | 63893 |
| rs769782554 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397790 | AGGGGGGTCTTGCCA[A/G]AGCCTCACCTGGGGC | 63893 |
| rs769801871 | snp | A/G | 1.73987e-05 | 0.00294942 | missense | UBE2O | GRCh38.p7 | 17:76396796 | TAGTCTGACTCCTCA[A/G]TCTCAGACTCTATGT | 63893 |
| rs769820292 | snp | A/C | 1.68846e-05 | 0.00290552 | missense | UBE2O | GRCh38.p7 | 17:76396635 | CCTTGTCCTCAGGGG[A/C]CACCGGCTGCTCCAG | 63893 |
| rs769841561 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | UBE2O | GRCh38.p7 | 17:76399545 | ATGCTCTTTTTGCGA[C/G]TCGTGCCGCTGCCGC | 63893 |
| rs769885486 | snp | C/T | 2.00258e-05 | 0.00316426 | missense | UBE2O | GRCh38.p7 | 17:76392017 | AGAAGTGGGGGGGCA[C/T]GGCTGGGTAGATGTT | 63893 |
| rs769889286 | snp | A/G | 1.65367e-05 | 0.00287543 | intron-variant | UBE2O | GRCh38.p7 | 17:76397778 | CACAAGCTCAGCAGG[A/G]GGGTCTTGCCAGAGC | 63893 |
| rs769903327 | snp | A/G | 1.76421e-05 | 0.00296998 | intron-variant | UBE2O | GRCh38.p7 | 17:76405327 | TGTCCTGGGGGAGGG[A/G]AGGAGACATGCAAGT | 63893 |
| rs769958198 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393599 | AACCCTTATCCCCAA[A/C]AAGGCAAGTAGTACA | 63893 |
| rs769964343 | snp | C/T | 4.97088e-05 | 0.00498517 | missense | UBE2O | GRCh38.p7 | 17:76405259 | TGATGCAGTTGGTGC[C/T]GATGAGCTTGACGGC | 63893 |
| rs769969299 | snp | C/T | 3.53851e-05 | 0.0042061 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76390961 | CTTGTCCTCTGTGCA[C/T]TCCGGCATGCCTGCC | 63893 |
| rs769975013 | snp | A/G | 1.65214e-05 | 0.0028741 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76395731 | CCTACTTGCCATTCT[A/G]TCTTCAAAAGTCTTG | 63893 |
| rs770012008 | in-del | -/G | 1.7736e-05 | 0.00297787 | intron-variant | UBE2O | GRCh38.p7 | 17:76405167 | GCCGAGAGAACCAGA[-/G]GGCCCAGAAAGGATG | 63893 |
| rs770064001 | snp | C/T | 8.24002e-05 | 0.0064182 | missense | UBE2O | GRCh38.p7 | 17:76396268 | TGCCCCTCGGGCTTG[C/T]CCTCCTTGCGCTCTA | 63893 |
| rs770092470 | snp | C/T | 3.35104e-05 | 0.00409317 | intron-variant | UBE2O | GRCh38.p7 | 17:76401002 | TCCTACCCTTGGGCC[C/T]GGACCCACCTCTTCC | 63893 |
| rs770124601 | in-del | -/CT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415794 | GGCAACAGAGCAAGA[-/CT]CTGTGTGTGTGTGTG | 63893 |
| rs770134258 | snp | A/C | 1.65089e-05 | 0.00287301 | missense, intron-variant | UBE2O | GRCh38.p7 | 17:76400176 | AGCCCTCCCCCTGGG[A/C]GCAGTTTTTTTCTGG | 63893 |
| rs770138058 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410839 | TGAGGCTGACCCCCA[A/G]TAACACAGCAAAAGC | 63893 |
| rs770140107 | in-del | -/GG | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451777 | GGTGTGAGATACAGG[-/GG]GGTGTGTGTGTGTGT | 63893 |
| rs770145956 | snp | G/T | 2.23997e-05 | 0.00334654 | intron-variant | UBE2O | GRCh38.p7 | 17:76400568 | GGGGATGGCAGGTGG[G/T]ACACGCCAGTCAGGG | 63893 |
| rs770230462 | snp | A/G | 2.80824e-05 | 0.00374705 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452924 | AGCCCGAAGTGCACG[A/G]AGCCACGGTAACGGC | 63893 |
| rs770248860 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420645 | AGACAAACTGGGCTG[C/G]GGCGCTGCAGACATT | 63893 |
| rs770251049 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441251 | TGAATAATCATTCTC[C/T]TCTTGGATTGGGTGT | 63893 |
| rs770260088 | snp | A/C/G/T | 8.26669e-05 | 0.00642871 | intron-variant | UBE2O | GRCh38.p7 | 17:76395868 | AATGATTTGCTAGAG[A/C/G/T]GGGGAAGAGAATAGT | 63893 |
| rs770266449 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397113 | GCATCTGTCCAAGGC[A/G]TTAGGGGACCTTGGC | 63893 |
| rs770299348 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427806 | CAGCTCCCTTGACAT[C/T]TCTCTGATCCCATGG | 63893 |
| rs770307143 | in-del | -/T | 1.65611e-05 | 0.00287755 | frameshift-variant | UBE2O | GRCh38.p7 | 17:76397874 | TCCACACGGGCCACC[-/T]TGGCCCACCGATGGC | 63893 |
| rs770344162 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439867 | CCTTCAGCATCTCAA[C/T]TGTGTCCTGCAGGTG | 63893 |
| rs770357785 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398369 | AACACTCACATCTTC[C/T]TCTTCTCCAATCAGC | 63893 |
| rs770376723 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426813 | TATTCAGATTTACCT[C/G]CACTTCCCAACGCCT | 63893 |
| rs770383488 | snp | A/T | 1.67125e-05 | 0.00289067 | missense | UBE2O | GRCh38.p7 | 17:76391398 | CCAGCCAGGACTCGA[A/T]ACGGTTCACCAGCCG | 63893 |
| rs770423421 | snp | C/T | 1.66225e-05 | 0.00288287 | missense, intron-variant | UBE2O | GRCh38.p7 | 17:76400156 | ACATACCTTCTTGGC[C/T]ATAGAGCCCTCCCCC | 63893 |
| rs770440523 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412482 | AGTGGCCAACTGGGG[C/G]TGTGGGAGAGACAGA | 63893 |
| rs770445613 | snp | C/G | 1.65663e-05 | 0.002878 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396192 | GGTGACGCCAGGCTT[C/G]CCGCCACACTGCTGG | 63893 |
| rs770449417 | snp | C/G | 3.29549e-05 | 0.00405911 | missense | UBE2O | GRCh38.p7 | 17:76398488 | TCCACGTCGTCCCCA[C/G]TCGGCCTCAGCTTGA | 63893 |
| rs770453955 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432381 | GATTGTATGGTCTCC[A/G]CCTTAGAAAGACTTA | 63893 |
| rs770510204 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76402191 | ACCAAAAAGTTGCGA[C/T]TCTGAGATGCCAATG | 63893 |
| rs770539583 | snp | A/C/T | 6.59189e-05 | 0.00574071 | missense | UBE2O | GRCh38.p7 | 17:76396277 | GGCTTGTCCTCCTTG[A/C/T]GCTCTACGTCGGGCA | 63893 |
| rs770544038 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413372 | ATTCCCCAAAGCAGC[A/G]CTTTTTTTCAAACCA | 63893 |
| rs770614554 | snp | A/G | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454840 | AAAACAAAAAACAAA[A/G]AAAAGGCTGGATGTG | 63893 |
| rs770671415 | snp | C/T | 1.66827e-05 | 0.00288809 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391408 | CTCGATACGGTTCAC[C/T]AGCCGCCAGCCACCA | 63893 |
| rs770673488 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399340 | CCCCGGAGCCACTAC[A/G]AGGCATGCAGAGGTG | 63893 |
| rs770718708 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443328 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 63893 |
| rs770724840 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76437449 | GCGAGATTCCATCTC[-/A]AAAAAAAAAAAAAAA | 63893 |
| rs770728015 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411727 | GTCTCACTCTGCCAC[C/T]CAGGTTGGAGGGCAG | 63893 |
| rs770744057 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441591 | TTGGAAGGGCCCATA[C/T]AAGTGCAATTCAAAA | 63893 |
| rs770891960 | snp | A/C/G | 5.25521e-05 | 0.00512579 | missense | UBE2O | GRCh38.p7 | 17:76399915 | GCTTCTTCAACAGGC[A/C/G]CTTCACCTGCAAGGG | 63893 |
| rs770899607 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439730 | TCTCTTGCCTTTATG[C/T]GCACTGGACTTCCCG | 63893 |
| rs770959050 | snp | C/G | 3.29875e-05 | 0.00406112 | missense | UBE2O | GRCh38.p7 | 17:76405517 | GCAGGACTCACGGTG[C/G]ATCGCATGTGCCGGA | 63893 |
| rs770988890 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404411 | CAGGAAGACCCAGGC[A/T]GAGGGTCAAATTACT | 63893 |
| rs770990450 | snp | A/G | 1.75946e-05 | 0.00296598 | intron-variant | UBE2O | GRCh38.p7 | 17:76405335 | GGGAGGGGAGGAGAC[A/G]TGCAAGTCCCGTGGT | 63893 |
| rs771039801 | snp | A/G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393054 | GCTTGAGGCCAGGAG[A/G/T]TCAAAACCAACCTGG | 63893 |
| rs771048936 | snp | A/G | 1.76927e-05 | 0.00297423 | intron-variant | UBE2O | GRCh38.p7 | 17:76400407 | CCCTGTCCCACGCGT[A/G]CCCCTGGGTTGCTGG | 63893 |
| rs771101417 | snp | C/T | 0.000379685 | 0.0137731 | missense | UBE2O | GRCh38.p7 | 17:76391062 | AGAGGGGGAAGCCGA[C/T]GTCAGGGTAGCCACT | 63893 |
| rs771134151 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423793 | CCAGGACATAATTGA[C/T]AGAGGTGGCCTACGG | 63893 |
| rs771181874 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417684 | CCTGGCAGAGAGCAC[C/T]ACGAAGGGCCTTCGA | 63893 |
| rs771187543 | snp | A/C/G | 6.61183e-05 | 0.00574938 | missense | UBE2O | GRCh38.p7 | 17:76391151 | GGCACCGATGCGTCT[A/C/G]GTGCGGTCTCCGAAG | 63893 |
| rs771189634 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76396921 | CGCACAGCTGATGGC[A/G]ACTGGGCTCATGAGG | 63893 |
| rs771202026 | snp | C/T | 4.95103e-05 | 0.00497521 | missense | UBE2O | GRCh38.p7 | 17:76391500 | TCATGGACTGCACCA[C/T]GCGGATCAGCGCCAT | 63893 |
| rs771233716 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429024 | CTCCTGCCTCAGCCT[A/C]CCGAGTAGCTGGGAT | 63893 |
| rs771268919 | snp | C/G/T | 5.08982e-05 | 0.0050445 | intron-variant | UBE2O | GRCh38.p7 | 17:76398798 | CCGGGCCCTCATTGG[C/G/T]GACCACCCTGCTGGC | 63893 |
| rs771285133 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427722 | TATAAACACAGACTT[A/G]GAACTTGGATGTTTT | 63893 |
| rs771318582 | snp | A/C/T | 8.26639e-05 | 0.00642856 | intron-variant | UBE2O | GRCh38.p7 | 17:76397783 | GCTCAGCAGGGGGGT[A/C/T]TTGCCAGAGCCTCAC | 63893 |
| rs771331138 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411621 | GACATGGGTGCTCTC[G/T]TTTAATCCCGGGGTA | 63893 |
| rs771417127 | snp | A/G | 0.00010525 | 0.00725355 | intron-variant | UBE2O | GRCh38.p7 | 17:76398627 | TAGCTAAGGGATCCC[A/G]GCTAAGGAGCCCACA | 63893 |
| rs771456790 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | UBE2O | GRCh38.p7 | 17:76399552 | TTTTGCGACTCGTGC[C/T]GCTGCCGCTCTGGGA | 63893 |
| rs771491856 | snp | C/G | 1.64779e-05 | 0.00287031 | missense | UBE2O | GRCh38.p7 | 17:76395790 | CCAGCAGCGCCATCT[C/G]CTTCCGCACTGTGCT | 63893 |
| rs771531901 | snp | A/G | 6.61989e-05 | 0.00575283 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76397859 | CACCTTGCTGCTGAC[A/G]TCCACACGGGCCACC | 63893 |
| rs771538002 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419526 | CCTTCGGCACTCCCT[C/G]ACACACCCTTCCTGT | 63893 |
| rs771570151 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412376 | AAACAATCTGAGAAA[C/T]GCCACTCCTCCACCC | 63893 |
| rs771590915 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421988 | CACAAATCCCAGGTG[A/G]AGGAAAATGGGAAGA | 63893 |
| rs771609438 | snp | C/T | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452457 | AAATCTCGAGGCCGA[C/T]ACCACAGCATAACAT | 63893 |
| rs771684298 | snp | A/G/T | 0.000181422 | 0.00952262 | stop-gained, synonymous-codon | UBE2O | GRCh38.p7 | 17:76391522 | CAGCGCCATCTCATT[A/G/T]TAACAGCGACTGTTT | 63893 |
| rs771769848 | in-del | -/AT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443284 | AAAAAGTTGGGGAAT[-/AT]ATATATATATATTTT | 63893 |
| rs771793896 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76398134 | GCTGCCCTTCTGAGG[A/G]CACTGAGCCCAGAGG | 63893 |
| rs771794330 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421640 | AAGGTGCTAGGATTA[C/T]AGGCGTGAGCCACCA | 63893 |
| rs771866571 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420953 | CCCCCCACATCCCTG[A/C]AATTAGGTCAGGACA | 63893 |
| rs771889192 | snp | G/T | 1.65375e-05 | 0.0028755 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400263 | GCTCCCCAAGCTGCC[G/T]CTGAGCATGGTCAAA | 63893 |
| rs771918334 | snp | A/G | 1.69568e-05 | 0.00291172 | intron-variant | UBE2O | GRCh38.p7 | 17:76395690 | CTGGGTGCCCACACA[A/G]CACATCTGCACCTGC | 63893 |
| rs771963855 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415942 | GTATATACGTATGCG[C/T]ATACATATGCACATA | 63893 |
| rs771991431 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441101 | TGGGTTTCAGTCTTT[C/T]CTTTTCTAAAATGGG | 63893 |
| rs772007963 | snp | G/T | 1.80208e-05 | 0.00300168 | missense | UBE2O | GRCh38.p7 | 17:76390950 | CCTGGCAGCTACTTG[G/T]CCTCTGTGCACTCCG | 63893 |
| rs772009310 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435167 | GATCCAGATCCAGGT[C/T]TGTCTGAATCCAAAG | 63893 |
| rs772022547 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444092 | CGGACGTGGTGGCGG[C/G]AGCCTGTAATCCCAG | 63893 |
| rs772024268 | snp | A/T | 1.64825e-05 | 0.00287071 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398523 | CTTCACCATGCAGGT[A/T]CGGCCGATGTGGTCC | 63893 |
| rs772062350 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396279 | CTTGTCCTCCTTGCG[C/T]TCTACGTCGGGCACT | 63893 |
| rs772082702 | snp | G/T | 5.7063e-05 | 0.00534118 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452748 | CCTTCACATGCTGCT[G/T]GACGCCCTCCGGGTA | 63893 |
| rs772084879 | snp | C/G | 1.76316e-05 | 0.00296909 | intron-variant | UBE2O | GRCh38.p7 | 17:76400415 | CACGCGTGCCCCTGG[C/G]TTGCTGGCAGTAAGG | 63893 |
| rs772172567 | snp | A/G | 1.81424e-05 | 0.00301179 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400535 | TCCATGTAACTTTCA[A/G]CTCTACAACCTGCAC | 63893 |
| rs772244529 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394130 | TAGCCCTGTTCCAGG[A/G]TTGTGGCTACTCCGG | 63893 |
| rs772249045 | snp | A/G | 3.35559e-05 | 0.00409595 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396660 | CTCCAGGGGTGGGAT[A/G]GGGGGCTCCTCTATC | 63893 |
| rs772266156 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438044 | CACACTGCTATTACC[A/G]GCAGGACCAGCCACC | 63893 |
| rs772266361 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449512 | CCCGGGAAGTTGAGG[C/T]TGTAATGAGCTGAGA | 63893 |
| rs772298331 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426023 | CCTTACATGCCTAAA[A/T]GGAGGGTCTCACTCT | 63893 |
| rs772333604 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421938 | GAGGACCCATCCCCT[-/C]CTCCAATGGATCTGC | 63893 |
| rs772338304 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407654 | TTCAGCCTAACAGCA[C/G]CCTTGGGAGTGCAGG | 63893 |
| rs772354372 | in-del | -/TTG | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454097 | CGATAAGCTTAACCA[-/TTG]TTGTACTATTTCCAA | 63893 |
| rs772413221 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430788 | TAAAGATCTGACAAA[A/G]GCAAAGAAGCTGCAA | 63893 |
| rs772499663 | snp | C/G | 1.64787e-05 | 0.00287038 | missense | UBE2O | GRCh38.p7 | 17:76399692 | TCTTTTAGCAGGAAT[C/G]GGGGCAGCTGCTCTC | 63893 |
| rs772509610 | snp | G/T | 1.65064e-05 | 0.00287279 | missense | UBE2O | GRCh38.p7 | 17:76391067 | GGGAAGCCGATGTCA[G/T]GGTAGCCACTCTTCT | 63893 |
| rs772519253 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417583 | CACACCCACCACCAG[C/T]GATAAGAGGACATGG | 63893 |
| rs772556513 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441667 | CACGCAGATTCTTCA[A/G]CCCAATGGAATTAGG | 63893 |
| rs772568120 | snp | G/T | 3.28036e-05 | 0.00404978 | missense | UBE2O | GRCh38.p7 | 17:76405524 | TCACGGTGGATCGCA[G/T]GTGCCGGACCACATC | 63893 |
| rs772587445 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76397871 | GACGTCCACACGGGC[C/T]ACCTGGCCCACCGAT | 63893 |
| rs772596021 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399159 | CTCACCCAGGGTTCC[A/G]AGGCCACGCATTCTC | 63893 |
| rs772649395 | in-del | -/TGGGAAGA | 1.65321e-05 | 0.00287502 | frameshift-variant | UBE2O | GRCh38.p7 | 17:76391042 | GAAACCCTTGGAAAG[-/TGGGAAGA]GGGGGAAGCCGATGT | 63893 |
| rs772658630 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422018 | ATGGAGATGTCTCAA[A/G]GGATCTGCTGTGTCC | 63893 |
| rs772680839 | snp | A/G | 1.64898e-05 | 0.00287135 | intron-variant | UBE2O | GRCh38.p7 | 17:76398247 | AGAACTTGAATTTGA[A/G]GGCGTACCTCATCCT | 63893 |
| rs772685617 | snp | A/G | 1.6516e-05 | 0.00287362 | intron-variant | UBE2O | GRCh38.p7 | 17:76398218 | CTGGTGCACAGGGCA[A/G]TGAGCAGCCATCCAG | 63893 |
| rs772704728 | snp | C/G | 9.13729e-05 | 0.00675856 | intron-variant | UBE2O | GRCh38.p7 | 17:76396039 | GGGGTCTGGCGAGGG[C/G]ACTAACCACCCTGCA | 63893 |
| rs772719647 | in-del | -/AA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429543 | GAGACTCTGTCTCAA[-/AA]AAAAAAAAAAAAAAA | 63893 |
| rs772740628 | snp | G/T | 1.67349e-05 | 0.0028926 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396171 | CTCGCCCTTGGCGCT[G/T]GTGAAGGTGACGCCA | 63893 |
| rs772764202 | snp | C/G | 1.64741e-05 | 0.00286998 | missense | UBE2O | GRCh38.p7 | 17:76398325 | TCAGTTGTACGGAAC[C/G]TAAAGTCAGGGTGGT | 63893 |
| rs772768774 | snp | C/T | 0.000161188 | 0.00897597 | intron-variant | UBE2O | GRCh38.p7 | 17:76400572 | ATGGCAGGTGGGACA[C/T]GCCAGTCAGGGCAGG | 63893 |
| rs772808134 | snp | A/G | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454568 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCAGAA | 63893 |
| rs772824180 | in-del | -/TCTCCTA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440164 | ACAGCGATGGTTCTC[-/TCTCCTA]TCTAAGTCTCTGAAG | 63893 |
| rs772837367 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409799 | GGAGCAGCAAACAAC[A/G]CAGTTGCCCTCCGAG | 63893 |
| rs772839520 | snp | C/T | 4.52049e-05 | 0.00475399 | intron-variant | UBE2O | GRCh38.p7 | 17:76396092 | GGAGCCCCGAGAAGG[C/T]GGGGGAAGGCGAAGA | 63893 |
| rs772853543 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424034 | TGCCTCAGCCTCCTG[A/C]GTAGCTGGGACTACA | 63893 |
| rs772859675 | snp | A/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452555 | GGCGTGTGCGCCCAG[A/G]GCTGCTGCAATGACT | 63893 |
| rs772874207 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447428 | GAGTGCCTGGCACAC[A/G]GTAACAGTATCCTGG | 63893 |
| rs772898775 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442292 | TACGTCCCAGTCCTG[A/G]AGTAATTATTCATAG | 63893 |
| rs772937702 | snp | A/G | 0.000107724 | 0.00733828 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452790 | GCACGTAGCCGCGGC[A/G]CAGGGGGCTGGCCCG | 63893 |
| rs772951276 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400067 | CCAAGGCCTAAAGCA[C/T]AGACTGTCCTTCTTG | 63893 |
| rs772952635 | snp | G/T | 1.64784e-05 | 0.00287035 | intron-variant | UBE2O | GRCh38.p7 | 17:76402594 | GCTCTCTGGTGGTGA[G/T]ACTCTACCTGGCGCC | 63893 |
| rs772990267 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438880 | GCATGCATAGGTGAC[A/G]CCATGCACACCGAGG | 63893 |
| rs772996220 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446006 | AGTTAAAAATACCGA[C/G]ATCCTATTAAGTGAG | 63893 |
| rs773021511 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76398149 | ACACTGAGCCCAGAG[A/G]ACTTTCAGGTCTTGT | 63893 |
| rs773027349 | snp | C/T | 0.000151412 | 0.0086996 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452940 | AGCCACGGTAACGGC[C/T]CGACACCAGGTCGTG | 63893 |
| rs773057229 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403517 | GCTCAAGTGATCCAT[C/G]TGCCTCAGCCTCTCA | 63893 |
| rs773063832 | snp | G/T | 3.29549e-05 | 0.00405911 | missense | UBE2O | GRCh38.p7 | 17:76399720 | CTCCTGCCTCGTGGG[G/T]CTCCTCTGCACCCTC | 63893 |
| rs773097201 | snp | C/G | 1.6676e-05 | 0.00288751 | missense | UBE2O | GRCh38.p7 | 17:76396545 | CAGCCTTCTCCATCA[C/G]CCCGGCCATGGGGGC | 63893 |
| rs773128451 | snp | A/G | 1.65356e-05 | 0.00287533 | intron-variant | UBE2O | GRCh38.p7 | 17:76397780 | CAAGCTCAGCAGGGG[A/G]GTCTTGCCAGAGCCT | 63893 |
| rs773152578 | snp | C/T | 1.65641e-05 | 0.00287781 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405266 | GTTGGTGCCGATGAG[C/T]TTGACGGCACAGTCG | 63893 |
| rs773171755 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421017 | CCAACAAAAATAAAT[A/G]CAAACACATAGCAGC | 63893 |
| rs773189197 | snp | C/T | 4.97294e-05 | 0.0049862 | intron-variant | UBE2O | GRCh38.p7 | 17:76391729 | CGGCCCTCCCTTGTC[C/T]GCACCCCCGCTTCAG | 63893 |
| rs773214222 | snp | A/G | 1.89525e-05 | 0.00307829 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390896 | GGGAGTGAGCAGGCG[A/G]CGGCTGGCCTCTCCC | 63893 |
| rs773277602 | snp | C/T | 1.66018e-05 | 0.00288108 | intron-variant | UBE2O | GRCh38.p7 | 17:76391846 | CCATCAATTCTGTTC[C/T]CCAGGCCCCTATCCA | 63893 |
| rs773321122 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395156 | GCTGGGATTACAGTC[A/G]TGAGCCACCGCACCC | 63893 |
| rs773327802 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76395755 | AGTCTTGACCATGAT[A/G]CCCTCAGGCAGTGAG | 63893 |
| rs773337986 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394146 | TTGTGGCTACTCCGG[A/G]CCCATCTCAACAGCA | 63893 |
| rs773345721 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449565 | GGGTGACAGAGAGAG[A/G]CTCTGTTTAAAAAAG | 63893 |
| rs773347008 | in-del | -/AAACTT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438370 | ACAATTAAAAAAGAA[-/AAACTT]AAACTTAAAGGCTCC | 63893 |
| rs773413223 | snp | A/G/T | 5.22301e-05 | 0.00511006 | intron-variant | UBE2O | GRCh38.p7 | 17:76405330 | CCTGGGGGAGGGGAG[A/G/T]AGACATGCAAGTCCC | 63893 |
| rs773453948 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411352 | ATGTCCCTGTAGGAG[C/T]GGATGGCTCCTAAAG | 63893 |
| rs773492195 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438113 | TCCCTCTTCTTACTG[A/C]CTTTTGGTAGGTGAC | 63893 |
| rs773500234 | snp | A/G | 1.65051e-05 | 0.00287267 | synonymous-codon, intron-variant | UBE2O | GRCh38.p7 | 17:76400177 | GCCCTCCCCCTGGGC[A/G]CAGTTTTTTTCTGGA | 63893 |
| rs773503093 | in-del | -/GAG | 5.24526e-05 | 0.00512089 | intron-variant | UBE2O | GRCh38.p7 | 17:76405185 | CCCAGAAAGGATGAT[-/GAG]AAGACAGGGCCGGCT | 63893 |
| rs773572135 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448471 | AGCCAAAAATAAACT[A/G]CAAAGCCAATTCCCG | 63893 |
| rs773592316 | snp | A/G | 1.64906e-05 | 0.00287142 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398541 | GCCGATGTGGTCCCC[A/G]GACTGTACCACACCG | 63893 |
| rs773633267 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417517 | GAGTATTAACCACCT[-/C]CTTGTTAATATGGTC | 63893 |
| rs773650309 | in-del | -/GC | | | frameshift-variant | UBE2O | GRCh38.p7 | 17:76396641 | CCTCAGGGGCCACCG[-/GC]TGCTCCAGGGGTGGG | 63893 |
| rs773678422 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420789 | TCCTGCCAGCATTCA[A/C]AATCGGCCTGCCACA | 63893 |
| rs773695244 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430988 | TCGTGCATAAGTTTC[C/T]TCCCTGCCTTTTGAA | 63893 |
| rs773697285 | snp | A/G | 1.70688e-05 | 0.00292132 | intron-variant | UBE2O | GRCh38.p7 | 17:76399426 | GCTGACGCCATTGGG[A/G]AGGGGCACAACTCTG | 63893 |
| rs773740892 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417588 | CCACCACCAGTGATA[A/G]GAGGACATGGATGGA | 63893 |
| rs773753876 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399176 | GGCCACGCATTCTCT[C/G]AGAACAGGATCCACT | 63893 |
| rs773791147 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434891 | CCTCCATCGGTGGTA[A/C]CTCTGGCTACTGAGA | 63893 |
| rs773808516 | snp | C/T | 3.29538e-05 | 0.00405904 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398490 | CACGTCGTCCCCACT[C/T]GGCCTCAGCTTGAAC | 63893 |
| rs773810377 | snp | C/T | 1.65578e-05 | 0.00287726 | missense | UBE2O | GRCh38.p7 | 17:76396194 | TGACGCCAGGCTTGC[C/T]GCCACACTGCTGGCA | 63893 |
| rs773900014 | snp | C/T | 7.34241e-05 | 0.0060586 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76453009 | AGTCCGAGGACGGCC[C/T]GGAGGCCGAGTCCGA | 63893 |
| rs773913812 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424130 | AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTTGT | 63893 |
| rs773929331 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408280 | GAGTTTTTCGCCTCA[C/T]GCTAACCAGGTGCTT | 63893 |
| rs773957079 | snp | C/T | 1.68482e-05 | 0.00290238 | missense | UBE2O | GRCh38.p7 | 17:76391344 | CCTTGGGCACCCCGT[C/T]GGGCAGTGCCTGGGC | 63893 |
| rs773973894 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440332 | TTCATCTCTTTGTTT[C/T]TTTTACTTTGAGACA | 63893 |
| rs773999310 | snp | A/G | 1.64871e-05 | 0.00287111 | intron-variant | UBE2O | GRCh38.p7 | 17:76402712 | GGGCTGCAGACCAAG[A/G]AGGCAGGGGCAGTGA | 63893 |
| rs774004444 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76402343 | TCACAGTGCCTCAAG[C/T]AAAGCATCAGCCTCT | 63893 |
| rs774022112 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443694 | CACAATGGAGCTATC[A/T]AGTAAGCAGCTGGGC | 63893 |
| rs774084349 | snp | A/G | 1.66521e-05 | 0.00288544 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76401041 | TCGGAACTTGCTCTT[A/G]GTGCTGAGCACGGGC | 63893 |
| rs774085826 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444922 | GTATTTGTGTGTCTA[C/T]ACTTCCCACCTGCAC | 63893 |
| rs774128745 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417464 | GGATTTTAGATACAC[C/T]AGGAGAGCTATCTGA | 63893 |
| rs774165966 | snp | C/T | 0.000199681 | 0.00999001 | missense | UBE2O | GRCh38.p7 | 17:76399453 | TCTGAGTTTACCTGT[C/T]CCCTGGCTTGAAGTC | 63893 |
| rs774174044 | snp | A/G | 3.46248e-05 | 0.00416068 | intron-variant | UBE2O | GRCh38.p7 | 17:76401186 | CAAAGGAAAGTCCCC[A/G]TGAGCGGTGTCTCCA | 63893 |
| rs774176756 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399802 | GGCAGACTCCGCTTC[A/G]CTCTTGGTTTTGGAT | 63893 |
| rs774193487 | snp | C/T | 6.21794e-05 | 0.00557547 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452802 | GGCGCAGGGGGCTGG[C/T]CCGGCCCTCCTCGTG | 63893 |
| rs774236105 | snp | A/G | 1.66283e-05 | 0.00288338 | intron-variant | UBE2O | GRCh38.p7 | 17:76391851 | AATTCTGTTCCCCAG[A/G]CCCCTATCCACCAGT | 63893 |
| rs774246717 | snp | A/G | 3.31565e-05 | 0.0040715 | intron-variant | UBE2O | GRCh38.p7 | 17:76395898 | TCAGTCCCTCATGGA[A/G]AGGCCCTGGAGCTCC | 63893 |
| rs774277235 | snp | C/G | 1.66751e-05 | 0.00288744 | intron-variant | UBE2O | GRCh38.p7 | 17:76400317 | TTGGGGAAGAAGTGG[C/G]GGTGAGCTGGGCTGG | 63893 |
| rs774284073 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | UBE2O | GRCh38.p7 | 17:76398382 | TCCTCTTCTCCAATC[A/G]GCTGTGGCACAGGAC | 63893 |
| rs774315192 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433784 | GCCAGCACTTTGGGA[C/G]GCCAAGGTAGGAGGA | 63893 |
| rs774365638 | snp | C/T | 1.72979e-05 | 0.00294086 | missense | UBE2O | GRCh38.p7 | 17:76390971 | GTGCACTCCGGCATG[C/T]CTGCCTCTAGCAGGG | 63893 |
| rs774372541 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76402188 | AGTACCAAAAAGTTG[A/C]GATTCTGAGATGCCA | 63893 |
| rs774443916 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436561 | CCTGAATCCCCGAGA[A/G]CCTAGACGATGCCTC | 63893 |
| rs774451530 | snp | A/C | 4.9534e-05 | 0.0049764 | missense | UBE2O | GRCh38.p7 | 17:76391065 | GGGGGAAGCCGATGT[A/C]AGGGTAGCCACTCTT | 63893 |
| rs774475802 | in-del | -/CCG | 2.06789e-05 | 0.00321543 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452712 | CGCGCCGCCCAGCCC[-/CCG]CCCGCCGCACCTTGG | 63893 |
| rs774546206 | snp | A/G | 3.64259e-05 | 0.00426751 | intron-variant | UBE2O | GRCh38.p7 | 17:76396834 | GTGCTGGGGGCAGAA[A/G]GGAAGTGCCAGGGTA | 63893 |
| rs774561880 | snp | C/T | 1.76783e-05 | 0.00297302 | intron-variant | UBE2O | GRCh38.p7 | 17:76400409 | CTGTCCCACGCGTGC[C/T]CCTGGGTTGCTGGCA | 63893 |
| rs774643651 | snp | C/T | 3.29641e-05 | 0.00405968 | missense | UBE2O | GRCh38.p7 | 17:76398918 | GGTCGTTGGAGCGGA[C/T]GTTGCATTCCACGGA | 63893 |
| rs774723942 | snp | C/T | 1.65537e-05 | 0.0028769 | missense | UBE2O | GRCh38.p7 | 17:76397866 | CTGCTGACGTCCACA[C/T]GGGCCACCTGGCCCA | 63893 |
| rs774724648 | snp | A/G | 1.64795e-05 | 0.00287045 | missense | UBE2O | GRCh38.p7 | 17:76396421 | GGCTCCACAGTCGGA[A/G]AGGTGGGCGAGCCCG | 63893 |
| rs774750780 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416052 | GTGTGTGTACATATG[C/T]ACATACACGTATATA | 63893 |
| rs774766037 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441541 | GCCTCGAACCAAAGA[C/T]GTACTAAAACTGAAC | 63893 |
| rs774853600 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76398031 | AATGTAACCAGCGGC[A/G]GCTCAAGAAGCCTGA | 63893 |
| rs774872378 | snp | A/C | 1.77454e-05 | 0.00297866 | intron-variant | UBE2O | GRCh38.p7 | 17:76405338 | AGGGGAGGAGACATG[A/C]AAGTCCCGTGGTGCA | 63893 |
| rs774906489 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411178 | CACCATGCTTGGCTA[A/C]TTTTTGTAATTTTTT | 63893 |
| rs774908479 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397362 | CTCCAACCAGGAGGC[A/G]AGGGAAGGAGAGCCC | 63893 |
| rs774922034 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76395791 | CAGCAGCGCCATCTC[C/T]TTCCGCACTGTGCTG | 63893 |
| rs774934424 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444764 | ACCAGAGAAATGCTT[C/T]CTTCCTTGGCTTGAA | 63893 |
| rs774943703 | snp | A/G | 1.6593e-05 | 0.00288031 | missense | UBE2O | GRCh38.p7 | 17:76391434 | CACCAGTGCTAAAGT[A/G]TTGCCTGATCTCCTG | 63893 |
| rs775018554 | snp | C/G | 1.64776e-05 | 0.00287028 | missense | UBE2O | GRCh38.p7 | 17:76399700 | CAGGAATGGGGGCAG[C/G]TGCTCTCCTGCCTCG | 63893 |
| rs775026016 | snp | A/G | 3.29511e-05 | 0.00405887 | missense | UBE2O | GRCh38.p7 | 17:76396398 | TCTTCTCCCGAGTTG[A/G]CTTCTCAGGCTCCAC | 63893 |
| rs775042631 | snp | A/G | 3.48639e-05 | 0.00417501 | intron-variant | UBE2O | GRCh38.p7 | 17:76401193 | AAGTCCCCGTGAGCG[A/G]TGTCTCCATGGGTGA | 63893 |
| rs775080147 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433483 | GTTTCTTTTTAGGGT[A/G]ATGAAAATGTTCTAA | 63893 |
| rs775084525 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447792 | CCCGCCTCGTGCACC[-/T]TTTGCTTCCCAAGGT | 63893 |
| rs775107565 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449834 | CTGAGGTAGGAGAAT[C/T]GCTTGAACCCGGGAG | 63893 |
| rs775190265 | snp | C/T | 5.34307e-05 | 0.00516841 | missense | UBE2O | GRCh38.p7 | 17:76390957 | GCTACTTGTCCTCTG[C/T]GCACTCCGGCATGCC | 63893 |
| rs775202975 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432705 | AGACTCCATGGGAGA[A/G]AGGGAAGATCCAAAT | 63893 |
| rs775208852 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | UBE2O | GRCh38.p7 | 17:76399597 | TGGCAGAGGAGGTCA[C/T]CGAACTGGTGTCGTC | 63893 |
| rs775214887 | snp | C/T | 1.64846e-05 | 0.0028709 | missense | UBE2O | GRCh38.p7 | 17:76398528 | CCATGCAGGTACGGC[C/T]GATGTGGTCCCCAGA | 63893 |
| rs775237233 | snp | A/G | 0.00626953 | 0.0556368 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76453067 | TGCGGCTGGGGCCGG[A/G]ACTGCCTCCGGGGCT | 63893 |
| rs775245265 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419991 | ACCTCCCTGCAACTG[C/T]GAATGCACAGAAGCA | 63893 |
| rs775295354 | snp | A/G | 1.65263e-05 | 0.00287452 | missense | UBE2O | GRCh38.p7 | 17:76397812 | ACCTGGGGCAGGATG[A/G]TGGTCTTTGAGTTGT | 63893 |
| rs775305144 | snp | A/G | 1.64803e-05 | 0.00287052 | missense | UBE2O | GRCh38.p7 | 17:76396283 | TCCTCCTTGCGCTCT[A/G]CGTCGGGCACTGCTT | 63893 |
| rs775308902 | snp | A/G | 1.89669e-05 | 0.00307946 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390893 | GGGGGGAGTGAGCAG[A/G]CGGCGGCTGGCCTCT | 63893 |
| rs775323079 | snp | G/T | 1.64741e-05 | 0.00286998 | intron-variant | UBE2O | GRCh38.p7 | 17:76398402 | TGGCACAGGACAGGT[G/T]GTCATGAGCTAGGGG | 63893 |
| rs775354420 | in-del | -/CAAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444231 | ATCTCACAAACAAAG[-/CAAAA]CAAAACAAAACAAAA | 63893 |
| rs775424795 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399399 | GGGGACGCGCACTCT[A/G]CCTGGCTTCACGCTG | 63893 |
| rs775426820 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413560 | GTTCAGTTGCATATA[C/T]AACACGTATGTGTCC | 63893 |
| rs775490927 | snp | A/G | 1.67489e-05 | 0.00289381 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396558 | CAGCCCGGCCATGGG[A/G]GCAGCCATGGCCACA | 63893 |
| rs775568492 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416018 | GTATGTGTATACATA[A/T]GTACACACACGTATA | 63893 |
| rs775696938 | snp | A/G | 1.66932e-05 | 0.002889 | intron-variant | UBE2O | GRCh38.p7 | 17:76399004 | ACCCTGCGGGTGCAG[A/G]CCAGTCAGCAGGCCA | 63893 |
| rs775756151 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435254 | CTAAAATATAAAAAA[C/G]GTATACTCACACACA | 63893 |
| rs775783105 | snp | C/G | 1.67719e-05 | 0.0028958 | missense | UBE2O | GRCh38.p7 | 17:76396661 | TCCAGGGGTGGGATG[C/G]GGGGCTCCTCTATCT | 63893 |
| rs775795423 | in-del | -/A | 1.66528e-05 | 0.0028855 | frameshift-variant | UBE2O | GRCh38.p7 | 17:76391054 | AGTGGGAAGAGGGGG[-/A]AAGCCGATGTCAGGG | 63893 |
| rs775817471 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | UBE2O | GRCh38.p7 | 17:76402609 | GACTCTACCTGGCGC[C/T]GTTGGATAGCTTCAG | 63893 |
| rs775817767 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436115 | AGCCAGGCATGGTGG[C/T]GTGCACCTGTAATCC | 63893 |
| rs775823261 | snp | C/T | 0.000204485 | 0.0101094 | intron-variant | UBE2O | GRCh38.p7 | 17:76405462 | GGCAGGCTCAAGTCC[C/T]TAAGGTGGCTGCCCC | 63893 |
| rs775825184 | snp | A/G | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454400 | TGAGGCAGGCAAATC[A/G]CTTGAACCTGGGAGG | 63893 |
| rs775839668 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450919 | GCTACCACACCCGGC[C/T]GTTGTTTTCGATTTA | 63893 |
| rs775855590 | snp | C/T | 0.00019859 | 0.00996271 | intron-variant | UBE2O | GRCh38.p7 | 17:76391736 | CCCTTGTCCGCACCC[C/T]CGCTTCAGCCCAACT | 63893 |
| rs775871116 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397336 | CAGGAGAGGAGAGCT[C/G]GGCTGTGTGGCTCCA | 63893 |
| rs775876087 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403652 | TATACATATAATACA[C/T]ATGTATTTCCTAGTG | 63893 |
| rs775909210 | snp | C/G | 3.28402e-05 | 0.00405204 | missense | UBE2O | GRCh38.p7 | 17:76405525 | CACGGTGGATCGCAT[C/G]TGCCGGACCACATCT | 63893 |
| rs775911597 | in-del | -/TATGTA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416214 | ATGTGTGTGTATATG[-/TATGTA]TATGTATATGTATAT | 63893 |
| rs775912985 | snp | A/G | 1.67357e-05 | 0.00289268 | intron-variant | UBE2O | GRCh38.p7 | 17:76400332 | GGGTGAGCTGGGCTG[A/G]ACTCCTGGGAGGCCA | 63893 |
| rs775917755 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395901 | GTCCCTCATGGAGAG[A/G]CCCTGGAGCTCCATC | 63893 |
| rs775947858 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441283 | TTATACTCAAAACAA[C/G]TACCATATTTACATC | 63893 |
| rs775970809 | snp | C/T | 4.97644e-05 | 0.00498796 | intron-variant | UBE2O | GRCh38.p7 | 17:76395905 | CTCATGGAGAGGCCC[C/T]GGAGCTCCATCTGCC | 63893 |
| rs775998140 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399362 | GCAGAGGTGTGTGTG[C/T]GAGCGCAGGCACGCA | 63893 |
| rs776104968 | snp | C/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390536 | CAGGGGAATTGTTGG[C/T]GCAACCCACACTTCA | 63893 |
| rs776162107 | in-del | -/AG | 1.66471e-05 | 0.00288501 | intron-variant | UBE2O | GRCh38.p7 | 17:76397913 | AAAGGGGACAAAGTC[-/AG]GGGGCCCAGCTCAAG | 63893 |
| rs776163768 | snp | C/T | 1.6495e-05 | 0.0028718 | intron-variant | UBE2O | GRCh38.p7 | 17:76398237 | GCAGCCATCCAGAAC[C/T]TGAATTTGAAGGCGT | 63893 |
| rs776181323 | snp | A/C | 4.24655e-05 | 0.00460771 | intron-variant | UBE2O | GRCh38.p7 | 17:76405585 | CAGCTGTAAAAGAAA[A/C]TACAGGTGTGAGAGA | 63893 |
| rs776182377 | snp | A/G | 3.29576e-05 | 0.00405928 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399715 | CTGCTCTCCTGCCTC[A/G]TGGGGCTCCTCTGCA | 63893 |
| rs776193375 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416952 | ATGGAGGCTACACAC[-/T]TGCAGGGGACAGAGA | 63893 |
| rs776273493 | snp | A/G | 1.66065e-05 | 0.00288149 | intron-variant | UBE2O | GRCh38.p7 | 17:76397900 | ATGGCTGCTGGGCAA[A/G]GGGGACAAAGTCAGG | 63893 |
| rs776282999 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442552 | GCTTTAGGATTTGCT[A/G]TCTCTGTTTCTCAAG | 63893 |
| rs776351322 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | UBE2O | GRCh38.p7 | 17:76396415 | TTCTCAGGCTCCACA[A/G]TCGGAGAGGTGGGCG | 63893 |
| rs776352907 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436348 | TGGTAGAATTATGGG[C/T]GACTTTTTTTTTACC | 63893 |
| rs776368072 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444451 | CTGAGGTGGGAGCAC[G/T]GCTTGAGCCCAGGAG | 63893 |
| rs776387974 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397294 | GGGCAAGCCATTCCC[A/G]CCCCCACTCCTGCCC | 63893 |
| rs776416647 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76405610 | GAGAGAATGGACTCT[A/G]AAGCCACCACAGAAT | 63893 |
| rs776437426 | snp | C/G | 1.80286e-05 | 0.00300233 | intron-variant | UBE2O | GRCh38.p7 | 17:76395945 | GGACAGGTGAGCACA[C/G]CCACAGACTTCCCAC | 63893 |
| rs776438824 | snp | C/T | 1.65031e-05 | 0.00287251 | missense | UBE2O | GRCh38.p7 | 17:76391559 | CCTTCCTGCAGGCCT[C/T]GGTCACTGTCGAAGC | 63893 |
| rs776581120 | snp | C/T | 1.68151e-05 | 0.00289953 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402097 | GCAGACGTCGTAGAG[C/T]TTGGCGCCATCTTCC | 63893 |
| rs776583286 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411737 | GCCACCCAGGTTGGA[A/G]GGCAGTGGCGCAAGC | 63893 |
| rs776636676 | snp | C/T | 1.68932e-05 | 0.00290625 | intron-variant | UBE2O | GRCh38.p7 | 17:76391875 | CACCAGTGGCTCTTC[C/T]TCCTTCTTGGCTGGG | 63893 |
| rs776662909 | snp | A/G | 5.02576e-05 | 0.00501261 | missense | UBE2O | GRCh38.p7 | 17:76396665 | GGGGTGGGATGGGGG[A/G]CTCCTCTATCTTGGG | 63893 |
| rs776692501 | snp | A/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454857 | AAAGGCTGGATGTGG[A/T]GGCTCTTGCCTGTAA | 63893 |
| rs776730506 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395584 | GACTGAGCCTGTGAC[C/T]GCCCCTGTAAAAGGT | 63893 |
| rs776750694 | snp | A/T | 1.70869e-05 | 0.00292286 | missense | UBE2O | GRCh38.p7 | 17:76396778 | CTGCCTTCTACCGAA[A/T]CGTAGTCTGACTCCT | 63893 |
| rs776785001 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419054 | TTGAGAGGCTGAGCT[C/T]TGAGAATCACTTAAG | 63893 |
| rs776790298 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419572 | AAAGACACAGAGGCA[A/C]CAGGTCCTCAAACTG | 63893 |
| rs776796873 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427769 | ACTTCCTCCAACACA[A/G]TCCAGAGTGTGGGGC | 63893 |
| rs776798727 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414401 | GATGAAATTACACCT[C/G]AAAACAGTTATACAC | 63893 |
| rs776835618 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439797 | GCTCTTATCTTTCAA[C/G]AGTGAACTCAAAAGG | 63893 |
| rs776839403 | snp | C/T | 1.73993e-05 | 0.00294947 | intron-variant | UBE2O | GRCh38.p7 | 17:76400434 | CTGGCAGTAAGGGCA[C/T]GCTTACCTGCCTAGG | 63893 |
| rs776890009 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441429 | GCGGATGATGAGTCC[A/G]CCTCATCCCTTTCCT | 63893 |
| rs776920459 | snp | C/G | 5.90557e-05 | 0.00543363 | missense | UBE2O | GRCh38.p7 | 17:76392008 | AGAGGTAGCAGAAGT[C/G]GGGGGGCACGGCTGG | 63893 |
| rs776927019 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407312 | AGAGGCATGCTGGCG[-/T]TGACGGTGCCACTTT | 63893 |
| rs776929846 | snp | C/T | 4.95405e-05 | 0.00497673 | intron-variant | UBE2O | GRCh38.p7 | 17:76402742 | AGACACAGCAGACAA[C/T]GTTCATGTCCAGGGC | 63893 |
| rs776955304 | in-del | -/AA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429542 | GTGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 63893 |
| rs776959034 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415359 | ACAGGAGACTGGGTG[C/G]CTTGGAGAAGTAAGT | 63893 |
| rs776980480 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438750 | ACATAACCAGTGTTT[C/T]CTCTTGCACTGGAAC | 63893 |
| rs776986203 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433633 | TAAGAGATGGGGTCT[C/T]GATCGCTTGAACCCA | 63893 |
| rs777015016 | in-del | -/GG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415566 | CCCAGCACTTTGAGA[-/GG]GGGCAAGGCGGTTGG | 63893 |
| rs777016078 | snp | C/T | 7.12746e-05 | 0.00596927 | intron-variant | UBE2O | GRCh38.p7 | 17:76399931 | CTTCACCTGCAAGGG[C/T]GGAGCAGAGAGGACA | 63893 |
| rs777022274 | snp | C/T | 1.65792e-05 | 0.00287912 | missense | UBE2O | GRCh38.p7 | 17:76405253 | GATAGATGATGCAGT[C/T]GGTGCCGATGAGCTT | 63893 |
| rs777028346 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415257 | CAAACTGATCCTGAC[A/G]GAGCCTGCCAGGAAA | 63893 |
| rs777039022 | snp | C/G | 4.78206e-05 | 0.00488958 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76452778 | ACCACTGGACGCGCA[C/G]GTAGCCGCGGCGCAG | 63893 |
| rs777067324 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76448666 | AGCTAAAGCATAAAC[C/G]CTTTGCCTCCGAAAC | 63893 |
| rs777099923 | snp | A/C/T | 0.000148074 | 0.00860341 | intron-variant | UBE2O | GRCh38.p7 | 17:76396084 | CACAAACAGGAGCCC[A/C/T]GAGAAGGCGGGGGAA | 63893 |
| rs777119817 | snp | G/T | 1.69092e-05 | 0.00290763 | missense | UBE2O | GRCh38.p7 | 17:76405212 | CCGGCTCACCCAGAT[G/T]TGCTGCAGGTCCTTG | 63893 |
| rs777128823 | snp | G/T | 8.29428e-05 | 0.0064393 | intron-variant | UBE2O | GRCh38.p7 | 17:76400556 | CAACCTGCACCTGGG[G/T]ATGGCAGGTGGGACA | 63893 |
| rs777139298 | in-del | -/TG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414262 | AAGCTGTGCTAAGAC[-/TG]AGGTCAACTGATTGA | 63893 |
| rs777145045 | in-del | -/ACAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447558 | AGACTCTGGAAACAT[-/ACAT]ACATACATACATACA | 63893 |
| rs777145853 | snp | C/T | 1.67522e-05 | 0.0028941 | intron-variant | UBE2O | GRCh38.p7 | 17:76399013 | GTGCAGGCCAGTCAG[C/T]AGGCCATGCAAACCC | 63893 |
| rs777185529 | snp | A/G | 1.65493e-05 | 0.00287652 | missense | UBE2O | GRCh38.p7 | 17:76391190 | GTGTGGTCCCTGCTA[A/G]CTGAGGCCAGGCCCT | 63893 |
| rs777201768 | in-del | -/GCTG | 3.34896e-05 | 0.0040919 | intron-variant | UBE2O | GRCh38.p7 | 17:76398826 | GGCTGCCCTTCCAGA[-/GCTG]GCACTACCTCGCTTA | 63893 |
| rs777202830 | in-del | -/TA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392635 | ATCTTATCAGGTGTT[-/TA]TTTCCTCATAAATCA | 63893 |
| rs777216417 | in-del | -/GGTGGTGA | 3.2962e-05 | 0.00405954 | intron-variant | UBE2O | GRCh38.p7 | 17:76402586 | AGCCGATGGCTCTCT[-/GGTGGTGA]GACTCTACCTGGCGC | 63893 |
| rs777234308 | in-del | -/C | 0.000147982 | 0.00860054 | intron-variant | UBE2O | GRCh38.p7 | 17:76396119 | AAGACCAGGCAAGGG[-/C]TGACTCACAGGGTGC | 63893 |
| rs777275481 | snp | C/T | 1.68125e-05 | 0.00289931 | missense | UBE2O | GRCh38.p7 | 17:76391302 | CTGACAGCTCGGCTA[C/T]AGCTGGGGGCTCTGG | 63893 |
| rs777313021 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393707 | CAGTGAGGGTTTGAA[C/G]TCCATGGGGGAGGTT | 63893 |
| rs777320974 | in-del | -/CA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413788 | ACAAAACCCAAGACC[-/CA]CACACAGTCACACTC | 63893 |
| rs777325560 | snp | A/G | 1.71855e-05 | 0.00293129 | intron-variant | UBE2O | GRCh38.p7 | 17:76400101 | ATGGAAATGGCTCAA[A/G]GCCAGTTCCTCAAAT | 63893 |
| rs777357634 | snp | A/G | 1.76955e-05 | 0.00297447 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391955 | ACACACCTTCCCATT[A/G]TCATACAGGTTGGGG | 63893 |
| rs777453460 | snp | C/G | 1.68644e-05 | 0.00290378 | intron-variant | UBE2O | GRCh38.p7 | 17:76392135 | AGGGAGGGAGGGAGG[C/G]AGGCCAAGGTTGGCA | 63893 |
| rs777456689 | snp | C/T | 1.85627e-05 | 0.00304647 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390928 | CGGTGATGCTCTTTC[C/T]TCTGTGCCTGGCAGC | 63893 |
| rs777488823 | snp | C/G | 1.66846e-05 | 0.00288826 | missense | UBE2O | GRCh38.p7 | 17:76391283 | GGTTCTTGTTGGCCG[C/G]AGTCTGACAGCTCGG | 63893 |
| rs777506157 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412389 | AACGCCACTCCTCCA[C/T]CCCCTCCCTGACCCC | 63893 |
| rs777512333 | in-del | -/G | 1.71064e-05 | 0.00292454 | intron-variant | UBE2O | GRCh38.p7 | 17:76401175 | GGATGTGGGGCCAAA[-/G]GAAAGTCCCCGTGAG | 63893 |
| rs777531984 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392983 | TATTCCTCAGCCAGA[C/T]GTGATGGCTCACACC | 63893 |
| rs777585778 | snp | A/G | 1.69591e-05 | 0.00291191 | intron-variant | UBE2O | GRCh38.p7 | 17:76400962 | AGCAGCTCAGCTCCA[A/G]GGTGTGGAGGTCAAG | 63893 |
| rs777664944 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450542 | CACCGAGCCACAAAA[C/T]GGATTTCAACAAATT | 63893 |
| rs777671379 | snp | A/C | 1.72027e-05 | 0.00293275 | intron-variant | UBE2O | GRCh38.p7 | 17:76399409 | ACTCTGCCTGGCTTC[A/C]CGCTGACGCCATTGG | 63893 |
| rs777725065 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404281 | GAGACCTGGTGGACA[A/C]CAACATGACCAGGGG | 63893 |
| rs777756089 | snp | A/C | 1.68946e-05 | 0.00290638 | missense | UBE2O | GRCh38.p7 | 17:76396638 | TGTCCTCAGGGGCCA[A/C]CGGCTGCTCCAGGGG | 63893 |
| rs777760884 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434187 | CAGCGAAATGACCCC[A/G]AGGATCCCTTCCAGT | 63893 |
| rs777792040 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | UBE2O | GRCh38.p7 | 17:76402680 | CAGTCATAGGCAATG[C/T]AGTCCCCATACATGA | 63893 |
| rs777812768 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | AANAT, UBE2O | GRCh38.p7 | 17:76453175 | TCGGGCGGCGGCGGC[G/T]ACAGCGGCGGCGAAC | 63893 |
| rs777826074 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407683 | GGGGAAACCGAGGTG[A/T]CAACTCTGAGGCTGA | 63893 |
| rs777839042 | snp | A/G | 8.4416e-05 | 0.00649622 | intron-variant | UBE2O | GRCh38.p7 | 17:76391622 | ATCAGACCTGTGTGG[A/G]CGGGACACCTTCCCT | 63893 |
| rs777847984 | snp | C/T | 1.66971e-05 | 0.00288934 | missense | UBE2O | GRCh38.p7 | 17:76396752 | ATTCATCCGAGGATG[C/T]CCCGCTGGTGCTGCC | 63893 |
| rs777850814 | snp | C/G | 1.67897e-05 | 0.00289733 | intron-variant | UBE2O | GRCh38.p7 | 17:76397940 | TCAAGCTCCAGCTCC[C/G]CAGCCCCTCCTGTGC | 63893 |
| rs777862117 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416857 | GACTCAAATACTAAC[C/T]AGAACAGCACCATCA | 63893 |
| rs777864406 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404767 | GGAAGAAAAAAGACC[A/G]GAGGGGGATCTCGGG | 63893 |
| rs777873761 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | UBE2O | GRCh38.p7 | 17:76399653 | GCGTCCTGCTCTGCC[A/G]AGTGCAGCCTGTCAT | 63893 |
| rs777928462 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446788 | GTTTTGCTCTAGGAG[A/G]TGGAGTTGGGGAATA | 63893 |
| rs778017204 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445735 | AGAGAGTTATCCAGT[A/T]ACACAATTCAATTTT | 63893 |
| rs778017940 | snp | A/G | 7.3888e-05 | 0.00607771 | intron-variant | UBE2O | GRCh38.p7 | 17:76396851 | GAAGTGCCAGGGTAA[A/G]CAGACAGGAAGTCAC | 63893 |
| rs778026805 | in-del | -/TC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428021 | TGCTTTGCTTTCGGT[-/TC]TCTGTTTTTCTTTCT | 63893 |
| rs778108432 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439512 | CATGATGTGTGATGA[C/T]GTCACTGCTCTGATG | 63893 |
| rs778138696 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444242 | AAAGCAAAACAAAAC[A/G]AAACAAAACAAAGAG | 63893 |
| rs778146894 | snp | C/T | 9.88745e-05 | 0.00703047 | missense | UBE2O | GRCh38.p7 | 17:76396275 | CGGGCTTGTCCTCCT[C/T]GCGCTCTACGTCGGG | 63893 |
| rs778228188 | snp | C/G | 1.65326e-05 | 0.00287507 | intron-variant | UBE2O | GRCh38.p7 | 17:76395865 | AAGAATGATTTGCTA[C/G]AGGGGGGAAGAGAAT | 63893 |
| rs778246422 | snp | A/C | 1.65304e-05 | 0.00287488 | missense | UBE2O | GRCh38.p7 | 17:76400253 | TACAGACAGCGCTCC[A/C]CAAGCTGCCGCTGAG | 63893 |
| rs778267928 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400044 | GCAAGGGTCATCAGG[A/G]CTGCCCCCCAAGGCC | 63893 |
| rs778327925 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403355 | GCTTAATGCAACCTC[C/T]ATCTTTGGGCTCAAG | 63893 |
| rs778357457 | in-del | -/TATG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416033 | GTACACACACGTATA[-/TATG]TATGTGTGTGTACAT | 63893 |
| rs778374395 | snp | G/T | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389133 | ACGTCGGCTCTCCCA[G/T]AACCTGGAAGGAGCT | 63893 |
| rs778382826 | snp | C/T | 4.957e-05 | 0.00497821 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391141 | CACACTGGGTGGCAC[C/T]GATGCGTCTGGTGCG | 63893 |
| rs778395640 | snp | A/G | | | missense | UBE2O | GRCh38.p7 | 17:76396394 | AACTTCTTCTCCCGA[A/G]TTGGCTTCTCAGGCT | 63893 |
| rs778439788 | snp | A/G | 3.39104e-05 | 0.00411753 | missense | UBE2O | GRCh38.p7 | 17:76402065 | ATGGAGCACACTACC[A/G]AGTCGCTGACGTGCG | 63893 |
| rs778460363 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446699 | GGACAGGAGGTCAAG[C/T]TGGAGCTCCTAATGG | 63893 |
| rs778511049 | snp | C/T | 3.62247e-05 | 0.0042557 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76390946 | TGTGCCTGGCAGCTA[C/T]TTGTCCTCTGTGCAC | 63893 |
| rs778534429 | snp | A/T | 1.69994e-05 | 0.00291538 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396771 | GCTGGTGCTGCCTTC[A/T]ACCGAATCGTAGTCT | 63893 |
| rs778542164 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392681 | ATTCCAGCTGGGCGC[A/G]GTGGTTCGTGCCTGT | 63893 |
| rs778598797 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403278 | TTTTACTTTATTATT[-/A]TTTTTTTTAGAGACA | 63893 |
| rs778601048 | snp | A/G | 1.6588e-05 | 0.00287988 | missense | UBE2O | GRCh38.p7 | 17:76391014 | GCGTCAGGACACCCC[A/G]GATGCTCTTGATGAA | 63893 |
| rs778607011 | in-del | -/ACC | 1.79059e-05 | 0.00299209 | intron-variant | UBE2O | GRCh38.p7 | 17:76402176 | GGGGACACAGTGAGT[-/ACC]AAAAAGTTGCGATTC | 63893 |
| rs778638385 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | UBE2O | GRCh38.p7 | 17:76399516 | TGCGCTTTAAGTTCT[G/T]GATGGACAAGGGGAT | 63893 |
| rs778730805 | snp | C/T | 1.68046e-05 | 0.00289862 | | | GRCh38.p7 | 17:76405306 | TCGATCACCGTGCCA[C/T]ACTGACTGTCCTGGG | 63893 |
| rs778741258 | snp | A/G | | | | | GRCh38.p7 | 17:76415939 | CACGTATATACGTAT[A/G]CGTATACATATGCAC | 63893 |
| rs778767392 | in-del | -/AAAGAGT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412352 | AACTTGATACTTCCC[-/AAAGAGT]AAAAACAATCTGAGA | 63893 |
| rs778786931 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428726 | TGATGGAAGAGTTGT[A/G]TATCTTGACTGCTGT | 63893 |
| rs778898637 | snp | C/T | 3.29495e-05 | 0.00405877 | missense | UBE2O | GRCh38.p7 | 17:76398287 | GAGCCCCATCCTCAG[C/T]ATTGCCGATGCGGAT | 63893 |
| rs778899779 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417319 | AGGCCCCCATGGCTG[A/G]GGCACCAGGGCAGGT | 63893 |
| rs778907795 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440839 | AGTTGTTGTGAAGGA[A/G]ACAGTATAGCCTGCA | 63893 |
| rs778909094 | snp | A/T | 3.39461e-05 | 0.00411969 | intron-variant | UBE2O | GRCh38.p7 | 17:76395687 | GCACTGGGTGCCCAC[A/T]CAGCACATCTGCACC | 63893 |
| rs778911572 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76427496 | GTGTTTGTTGTGATC[A/G]CTGACTCATGTTCTA | 63893 |
| rs778963286 | in-del | -/CTT | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389929 | CCTCTCGGCCTGGAG[-/CTT]CTTCACATTATCAAA | 63893 |
| rs778988244 | snp | G/T | 5.56901e-05 | 0.00527655 | intron-variant | UBE2O | GRCh38.p7 | 17:76396117 | CGAAGACCAGGCAAG[G/T]GCTGACTCACAGGGT | 63893 |
| rs779019194 | snp | A/G | 3.45352e-05 | 0.00415528 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400515 | TGGACAGAAACTCTT[A/G]GTAATCCATGTAACT | 63893 |
| rs779022607 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432244 | CCATGTCTTAGACCC[A/G]TCAAACTGCTACGGA | 63893 |
| rs779035081 | snp | C/T | 7.34187e-05 | 0.00605838 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452737 | CACCTTGGTCTCCTT[C/T]ACATGCTGCTTGACG | 63893 |
| rs779088980 | snp | C/T | 3.09162e-05 | 0.00393156 | intron-variant | UBE2O | GRCh38.p7 | 17:76396033 | GTAGCTGGGGTCTGG[C/T]GAGGGGACTAACCAC | 63893 |
| rs779090372 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442201 | GCCTGGGGAGCCCGC[A/G]ACGGAAGTTGCCAAA | 63893 |
| rs779167923 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426232 | TGGTCTCGAACGGGG[A/C]TCAAGCGATCCTCCT | 63893 |
| rs779195481 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76422812 | CAGTCTGTGTGCCCC[A/G]TGGGGGTTAGAATGT | 63893 |
| rs779200991 | snp | C/G | 1.65154e-05 | 0.00287358 | missense | UBE2O | GRCh38.p7 | 17:76396495 | CTTGATGGCCTCTTT[C/G]AACTCCCGGAAGCTC | 63893 |
| rs779246810 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449300 | TTCAATGGGGCAAGG[C/G]ACTGTGGCTTATGCC | 63893 |
| rs779255683 | in-del | -/AGA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449365 | GAATCACTTGAGGCC[-/AGA]AGTTCAAGACCAGCC | 63893 |
| rs779276300 | snp | C/T | 4.95045e-05 | 0.00497492 | missense | UBE2O | GRCh38.p7 | 17:76391502 | ATGGACTGCACCACG[C/T]GGATCAGCGCCATCT | 63893 |
| rs779363008 | snp | A/G | 1.65244e-05 | 0.00287436 | missense | UBE2O | GRCh38.p7 | 17:76391142 | ACACTGGGTGGCACC[A/G]ATGCGTCTGGTGCGG | 63893 |
| rs779393512 | snp | A/G | 9.89087e-05 | 0.00703168 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398874 | TCCAGGGCAGAACTC[A/G]TTGTTGTCCAGGTGG | 63893 |
| rs779406266 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426504 | TTTTTCTTTGCTCTC[-/T]TTTCTTTTAGACAAA | 63893 |
| rs779415520 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412294 | AGACCAGATTCCTAA[A/C]AGGAAGATGAGGTTA | 63893 |
| rs779478822 | snp | A/G | 1.75677e-05 | 0.00296371 | intron-variant | UBE2O | GRCh38.p7 | 17:76402164 | TGGTCTCCACCAGGG[A/G]ACACAGTGAGTACCA | 63893 |
| rs779480785 | snp | C/G | 6.59109e-05 | 0.0057403 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399673 | CAGCCTGTCATCTCT[C/G]CCTTCTTTTAGCAGG | 63893 |
| rs779568832 | snp | A/C | 1.64781e-05 | 0.00287033 | missense | UBE2O | GRCh38.p7 | 17:76399755 | TGCATCTCCACTGGA[A/C]TGGCAGAGCCATCGG | 63893 |
| rs779578370 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414940 | AGGGAGGGGACAGAT[G/T]GGCATCTTTAGGAGA | 63893 |
| rs779579318 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | UBE2O | GRCh38.p7 | 17:76399038 | AAACCCCACCCCCTC[C/T]GCGGAAAGGGCAGAG | 63893 |
| rs779581056 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413152 | AGACAAGAATACAAA[C/T]ATAAAATAAGGTACA | 63893 |
| rs779614229 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415868 | ATATATATACATACA[C/T]GTATATACAAATATA | 63893 |
| rs779645105 | snp | A/G | 6.81443e-05 | 0.00583674 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76390981 | GCATGCCTGCCTCTA[A/G]CAGGGCAGCCCGGAA | 63893 |
| rs779665358 | in-del | -/TGTGTGTACATATGTACATACACGTATATACGTA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416037 | ACACACGTATATATG[lengthTooLong]TGTGTGTACATATGT | 63893 |
| rs779665760 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76428671 | GTTATTCTTGGCATC[C/T]ATTCCTATTTAAAAG | 63893 |
| rs779667761 | snp | C/T | 1.65269e-05 | 0.00287457 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398967 | GTCGGCTGAGGTCAT[C/T]GTGGTCACCACCTCC | 63893 |
| rs779668642 | snp | A/G | 1.69095e-05 | 0.00290765 | intron-variant | UBE2O | GRCh38.p7 | 17:76395698 | CCACACAGCACATCT[A/G]CACCTGCCCATGCCA | 63893 |
| rs779697750 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403227 | CTGAGGTGTTTAGGT[A/G]GAAGTGGATCTATCA | 63893 |
| rs779721542 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446954 | GGAATGAAAAGAGTG[G/T]AATCTGCAGAAGCAC | 63893 |
| rs779756024 | snp | A/C | 1.6857e-05 | 0.00290314 | missense | UBE2O | GRCh38.p7 | 17:76396614 | CCTCTTCACTGATCA[A/C]CACTCCCTTGTCCTC | 63893 |
| rs779778170 | snp | A/G | 1.64868e-05 | 0.00287109 | intron-variant | UBE2O | GRCh38.p7 | 17:76402571 | AGGCTATCCTTCCCA[A/G]GCCGATGGCTCTCTG | 63893 |
| rs779805101 | in-del | -/AA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425927 | TTCCTGGATCCTGGG[-/AA]AAGTCCCTGGTTTTG | 63893 |
| rs779928290 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76430554 | ACAGTATAGAGCTCA[C/T]GAATCAGATCCTCGA | 63893 |
| rs779929137 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439398 | GAAACCCTTTCAGGA[A/G]GTCCAAAGTCAAAAA | 63893 |
| rs779971930 | snp | G/T | 0.00324148 | 0.0401277 | intron-variant | UBE2O | GRCh38.p7 | 17:76405323 | CTGACTGTCCTGGGG[G/T]AGGGGAGGAGACATG | 63893 |
| rs779992436 | in-del | -/TA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416032 | ATGTACACACACGTA[-/TA]TATGTGTGTGTACAT | 63893 |
| rs780029767 | snp | A/G | 3.31307e-05 | 0.00406992 | missense | UBE2O | GRCh38.p7 | 17:76391049 | TTGGAAAGTGGGAAG[A/G]GGGGGAAGCCGATGT | 63893 |
| rs780040391 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76412112 | GACGACCAGCCCCAC[A/G]CTAGGTCCCTGGTGA | 63893 |
| rs780041876 | in-del | -/CCAT | 1.6838e-05 | 0.0029015 | intron-variant | UBE2O | GRCh38.p7 | 17:76395705 | CACATCTGCACCTGC[-/CCAT]CCATGCCAAGCCTAC | 63893 |
| rs780056240 | snp | A/G | 1.75953e-05 | 0.00296603 | intron-variant | UBE2O | GRCh38.p7 | 17:76398636 | GATCCCGGCTAAGGA[A/G]CCCACATCTCAAGCC | 63893 |
| rs780059889 | snp | A/G | 1.65427e-05 | 0.00287595 | missense | UBE2O | GRCh38.p7 | 17:76400268 | CCAAGCTGCCGCTGA[A/G]CATGGTCAAAGCATC | 63893 |
| rs780061841 | snp | G/T | 0.000179762 | 0.00947886 | intron-variant | UBE2O | GRCh38.p7 | 17:76405495 | GGCCCGGGGCTGGGG[G/T]GGGGACGCAGGACTC | 63893 |
| rs780077217 | snp | C/T | 1.90525e-05 | 0.00308641 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76400545 | TTTCAACTCTACAAC[C/T]TGCACCTGGGGATGG | 63893 |
| rs780127289 | snp | G/T | 1.67719e-05 | 0.0028958 | missense | UBE2O | GRCh38.p7 | 17:76391382 | AGCAGGGCATGGGTT[G/T]CCAGCCAGGACTCGA | 63893 |
| rs780167181 | snp | C/T | 1.68457e-05 | 0.00290216 | intron-variant | UBE2O | GRCh38.p7 | 17:76400985 | AGGTCAAGGACTCCA[C/T]CTCCTACCCTTGGGC | 63893 |
| rs780187409 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394632 | TGAAAATGTAAAAAT[-/A]TTTTTTTAGTGTATA | 63893 |
| rs780205983 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401659 | TGTGGGCAGATCACC[C/T]GAGGTCAAGAGTTCG | 63893 |
| rs780226906 | snp | A/G | 1.67368e-05 | 0.00289277 | missense | UBE2O | GRCh38.p7 | 17:76391292 | TGGCCGGAGTCTGAC[A/G]GCTCGGCTACAGCTG | 63893 |
| rs780234026 | snp | A/G | 1.76027e-05 | 0.00296665 | missense | UBE2O | GRCh38.p7 | 17:76396136 | GACTCACAGGGTGCA[A/G]ACTCCAGTACGGAGA | 63893 |
| rs780250841 | snp | C/G | 1.64754e-05 | 0.00287009 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402649 | GTTCTTCAAGTCGTA[C/G]ACCTTCCCCAGCCAG | 63893 |
| rs780266397 | snp | A/G | 0.00018528 | 0.00962319 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76401125 | CACCTGGCCTGGGTA[A/G]AAGCCATAGGAATCA | 63893 |
| rs780300652 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403700 | GTAGCAATTAGCACA[C/T]CTAGCATCCAGATCT | 63893 |
| rs780325970 | snp | A/T | 1.64836e-05 | 0.0028708 | missense | UBE2O | GRCh38.p7 | 17:76396253 | GCCTTCACAGGTGAC[A/T]GCCCCTCGGGCTTGT | 63893 |
| rs780343662 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76432138 | AGCATGGAGAATCTG[C/T]GAGGCAGCAGCAGCC | 63893 |
| rs780378619 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392399 | GCCTCCCAAGTAGCC[A/G]GGACTACAGTGTGGG | 63893 |
| rs780511654 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454089 | AGCTCCTTCGATAAG[C/T]TTAACCATTGTTGTA | 63893 |
| rs780516733 | snp | A/G | 1.68462e-05 | 0.00290221 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396633 | TCCCTTGTCCTCAGG[A/G]GCCACCGGCTGCTCC | 63893 |
| rs780561186 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421459 | CATAGCCTGCTTCCC[C/T]GGTTCAAGCGATTGT | 63893 |
| rs780562730 | snp | A/G | 9.90001e-05 | 0.00703493 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452761 | CTTGACGCCCTCCGG[A/G]TACCACTGGACGCGC | 63893 |
| rs780589787 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420609 | CTCCACTCCTTACAA[C/T]TCTGTAACTACATCT | 63893 |
| rs780612472 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420718 | GCCAAGGAGGAAGAG[A/C]CACAAGACGTCCTGG | 63893 |
| rs780616173 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435703 | AATCACAGGTCTACA[C/T]GCCCTCTCTAAGCCC | 63893 |
| rs780657034 | snp | A/C/G | 3.29594e-05 | 0.00405941 | intron-variant | UBE2O | GRCh38.p7 | 17:76402587 | GCCGATGGCTCTCTG[A/C/G]TGGTGAGACTCTACC | 63893 |
| rs780665804 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401559 | CTTAAAGGATGAGAA[A/G]AAAAAGCTACCAAAA | 63893 |
| rs780673641 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418482 | TGGAGGAAGTTTAGA[C/T]ATTCAATTCAGCAGT | 63893 |
| rs780701885 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76413490 | ACATGTGGTAAGAAT[-/A]AGTACTATTAGGTTG | 63893 |
| rs780742753 | snp | A/G | 3.295e-05 | 0.00405881 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402664 | GACCTTCCCCAGCCA[A/G]CAGTCATAGGCAATG | 63893 |
| rs780791562 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410667 | CTGGGCACTTCTGTT[A/G]TGCCCCATTTGAGCT | 63893 |
| rs780836511 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414714 | CCAACTGCCTGCTAA[A/G]TGAGGGGGAAGGACT | 63893 |
| rs780883248 | snp | C/T | 1.75786e-05 | 0.00296462 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391946 | GAGGCTGACACACAC[C/T]TTCCCATTGTCATAC | 63893 |
| rs780884414 | snp | C/T | 1.65553e-05 | 0.00287705 | missense | UBE2O | GRCh38.p7 | 17:76396731 | AGCTGTCACTATCAT[C/T]TTCCCATTCATCCGA | 63893 |
| rs780905935 | snp | C/G | 1.65157e-05 | 0.0028736 | missense | UBE2O | GRCh38.p7 | 17:76391059 | GGAAGAGGGGGAAGC[C/G]GATGTCAGGGTAGCC | 63893 |
| rs780907779 | snp | C/T | 1.6998e-05 | 0.00291525 | missense | UBE2O | GRCh38.p7 | 17:76399883 | GTCTGGGGAGCATGA[C/T]ATGATCCGCACAACC | 63893 |
| rs780909877 | snp | A/G | | | synonymous-codon, intron-variant | UBE2O | GRCh38.p7 | 17:76400159 | TACCTTCTTGGCCAT[A/G]GAGCCCTCCCCCTGG | 63893 |
| rs780956973 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435177 | CAGGTTTGTCTGAAT[C/T]CAAAGCTCTGACCTG | 63893 |
| rs780995965 | snp | C/T | 4.96052e-05 | 0.00497998 | missense | UBE2O | GRCh38.p7 | 17:76391146 | TGGGTGGCACCGATG[C/T]GTCTGGTGCGGTCTC | 63893 |
| rs781007644 | snp | A/C | 0.00140154 | 0.0264349 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452717 | CGCCCAGCCCCCGCC[A/C]GCCGCACCTTGGTCT | 63893 |
| rs781025772 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438431 | GGCACACTAATGTCC[C/T]TACTCCTGCTCTGTC | 63893 |
| rs781027844 | in-del | -/TGAC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446924 | CAGTTATTTTGAGAA[-/TGAC]TGAGGGGTCAGGGAA | 63893 |
| rs781098873 | snp | C/G | 3.54931e-05 | 0.00421251 | intron-variant | UBE2O | GRCh38.p7 | 17:76400404 | GAGCCCTGTCCCACG[C/G]GTGCCCCTGGGTTGC | 63893 |
| rs781102097 | snp | C/T | 1.70272e-05 | 0.00291776 | missense | UBE2O | GRCh38.p7 | 17:76400495 | CTGACGCTGTCCGTG[C/T]CCCCTGGACAGAAAC | 63893 |
| rs781115431 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410679 | GTTGTGCCCCATTTG[A/G]GCTCCCCGAAGCTAT | 63893 |
| rs781149933 | snp | C/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452247 | CTAGTGAACTTCTTG[C/G]GTTCGGCTGGGATTT | 63893 |
| rs781195216 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | UBE2O | GRCh38.p7 | 17:76398906 | GCACAGGGAAGAGGT[C/T]GTTGGAGCGGATGTT | 63893 |
| rs781235752 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76396970 | ACCCTTTCCCTGACC[A/T]CTGCTCTGGCTTTTG | 63893 |
| rs781252208 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445507 | CTTCTGAGTGGTATG[A/T]CAACTGACTGCAATG | 63893 |
| rs781277172 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407367 | CTGTAACCCTCTGTG[A/C]CCAAATCTCCACTCT | 63893 |
| rs781277181 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393729 | GGGGAGGTTGGGAGA[C/G]CACCGCTCCACAGAC | 63893 |
| rs781304812 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429026 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 63893 |
| rs781312595 | snp | C/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451852 | AAGCCACCAAACCAA[C/G]CCGGGTTCAAGGTTT | 63893 |
| rs781338351 | in-del | -/AGTT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435862 | GAGGGGACAGAAAAC[-/AGTT]AGCAAAAGGCCCAGT | 63893 |
| rs781364579 | snp | C/T | 1.67466e-05 | 0.00289362 | missense | UBE2O | GRCh38.p7 | 17:76391395 | TTTCCAGCCAGGACT[C/T]GATACGGTTCACCAG | 63893 |
| rs781396194 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397685 | TCCCCTCACGCTTTC[A/G]CTGAGATCTCACCAG | 63893 |
| rs781400239 | snp | A/G/T | 3.52269e-05 | 0.00419672 | intron-variant | UBE2O | GRCh38.p7 | 17:76397776 | GTCACAAGCTCAGCA[A/G/T]GGGGGTCTTGCCAGA | 63893 |
| rs781462210 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant | UBE2O | GRCh38.p7 | 17:76398440 | CCCAACCCCAGAGCC[C/T]ACCTGAAGCAAGCAG | 63893 |
| rs781484606 | snp | C/G | 0.00015259 | 0.00873337 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452908 | GTGGATGAGGCGCAC[C/G]AGCCCGAAGTGCACG | 63893 |
| rs781570499 | snp | C/G | 1.68035e-05 | 0.00289853 | intron-variant | UBE2O | GRCh38.p7 | 17:76400993 | GACTCCATCTCCTAC[C/G]CTTGGGCCCGGACCC | 63893 |
| rs781583542 | snp | C/T | 1.64743e-05 | 0.00287 | missense | UBE2O | GRCh38.p7 | 17:76398308 | CGATGCGGATGACGA[C/T]GTCAGTTGTACGGAA | 63893 |
| rs781607232 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76420992 | TAGTCTGCTTTCTAA[A/G]CCAAGATTTCCAACA | 63893 |
| rs781608288 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423537 | TCTCTACTAAAAATA[C/T]AAAAAATTAGCCAGG | 63893 |
| rs781637954 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434280 | GATGAAGACCCCACC[A/T]GCAATAAGCACACGG | 63893 |
| rs781726144 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433379 | TTATATGAAATGTCC[A/G]AAATAGGCAAACCCA | 63893 |
| rs781729333 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445567 | TACTGCTTCAGGAGA[A/G]CACAGCCTACCTGTG | 63893 |
| rs796072366 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395484 | GGTGTGAGCCACTGC[A/G]CCCGGCCGAGAAAGT | 63893 |
| rs796114561 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447850 | TCTCATGGAAGTGAT[A/C]TTCTGAAGGCACAGG | 63893 |
| rs796146368 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76449827 | CGGGAGGCTGAGGTA[C/G]GAGAATCGCTTGAAC | 63893 |
| rs796162221 | in-del | G/TT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443600 | GTCAGAACATTTTTT[G/TT]TTTTTTAAGTCCACA | 63893 |
| rs796178810 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76424395 | TTGTATTTTTGTAGA[A/G]ACAGGGTTTCACCAT | 63893 |
| rs796205017 | in-del | -/TT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433617 | TAAACCTTTTTTTTT[-/TT]AAGAGATGGGGTCTC | 63893 |
| rs796333709 | snp | C/T | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390786 | AGCATCTCAACACAC[C/T]TCTTGCACTTCAGCA | 63893 |
| rs796351894 | snp | G/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453866 | AAGCCAAGAATGAAT[G/T]GCAAGAGGTAGTATA | 63893 |
| rs796358041 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443608 | CATTTTTTTTTTTTT[-/T]AAGTCCACAGACTTG | 63893 |
| rs796360157 | in-del | -/AC | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389509 | TGCTAATGAGCCAAC[-/AC]AAAAAAAAAAAAAAA | 63893 |
| rs796360973 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76402781 | CTCTATGCCCCACCG[-/A]AGACAGGATGGGGGA | 63893 |
| rs796394314 | snp | C/T | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454135 | CTGCCTAGACTAAAT[C/T]CCAGACTGGCAGAAC | 63893 |
| rs796427148 | in-del | -/C | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389509 | GCTAATGAGCCAACA[-/C]CAAAAAAAAAAAAAA | 63893 |
| rs796555725 | in-del | AA/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446463 | AAACAAAAACAAACA[AA/C]AAAAAAAACCAAACA | 63893 |
| rs796590444 | in-del | -/CAGT | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390827 | TTGGGGAGAAGAGGG[-/CAGT]CAGTGGGTTTGCAGT | 63893 |
| rs796602054 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407701 | ACTCTGAGGCTGAAG[C/T]AGAAAAAAACAGCTG | 63893 |
| rs796662053 | in-del | -/AAAAAAAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425226 | CAAGGTCCTTTCGAC[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 63893 |
| rs796696738 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444734 | TGCTGGGATGACCCA[A/G]AAGCACACTGGGGGA | 63893 |
| rs796744098 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76406092 | CTAATCTGGGTTATC[C/T]TCCTGACCAGCTGCG | 63893 |
| rs796744162 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425238 | GACAAAAAAAAAAAA[-/AAAAAAAAAAAAA]GTAAAAGAAAAAAAT | 63893 |
| rs796749678 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394914 | GAAGTCTCGCTCTGT[-/T]GCCCAGGCTGGAGTG | 63893 |
| rs796776830 | in-del | AG/TAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443608 | ATTTTTTTTTTTTTT[AG/TAA]TCCACAGACTTGGGG | 63893 |
| rs796802134 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394419 | AGAGACACTAGGCCC[C/T]GTCCACGAACAGAGG | 63893 |
| rs796821276 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446464 | AAACAAAAACAAACA[-/A]AAAAAAAAACCAAAC | 63893 |
| rs796849127 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446473 | CAAACAAAAAAAAAA[-/A]CCAAACAAACAAAAC | 63893 |
| rs796880680 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434295 | TGCAATAAGCACACG[A/G]TGGCTGAAAACTCCT | 63893 |
| rs796996114 | in-del | -/TG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415796 | GCAACAGAGCAAGAC[-/TG]TGTGTGTGTGTGTGT | 63893 |
| rs797003147 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404628 | AACGTTGATTTCCCA[A/G]TCTGGGGGTTATATG | 63893 |