SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6747 | snp | A/G | 0.352721 | 0.227922 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378222 | TCCAGCCCCAGGACC[A/G]CAGCAGCAGCCAGGT | 51667 |
rs14684 | snp | A/G | 0 | 0 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378278 | TGCCTTCTGGAAGGG[A/G]GGGAAAGTCTTGGAT | 51667 |
rs365501 | snp | C/G | 0.0198 | 0.0975087 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341321 | GCCCACCAGGGGCTT[C/G]CCTGGGGTGAAATTA | 51667 |
rs365741 | snp | A/G | 0.367503 | 0.220665 | intron-variant | NUB1 | GRCh38.p7 | 7:151345691 | TGTAATCCTGTGATG[A/G]TATTAAAAATATATG | 51667 |
rs366355 | snp | A/G | 0.445127 | 0.156286 | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352145 | GGGCTGATCCACAGG[A/G]TCTTCTACGCATGTG | 51667 |
rs367191 | snp | A/G | 0.215446 | 0.2476 | intron-variant | NUB1 | GRCh38.p7 | 7:151367219 | CTACTGCCAGAAGGT[A/G]ATTTCATTTTGATAG | 51667 |
rs367547 | snp | A/G | 0.419616 | 0.183658 | intron-variant | NUB1 | GRCh38.p7 | 7:151353072 | TCCCACTATCATAGA[A/G]CAGACAGTAAATATT | 51667 |
rs367567 | snp | A/G | 0.48491 | 0.0855403 | intron-variant | NUB1 | GRCh38.p7 | 7:151367336 | GAGCATTTAGCCCAA[A/G]GGAACATGGTTTGCT | 51667 |
rs375192 | snp | C/T | 0.211516 | 0.24702 | intron-variant | NUB1 | GRCh38.p7 | 7:151353318 | ACTCCCCTCCCCTCA[C/T]TCTCCACACACAGCC | 51667 |
rs379931 | snp | A/G | 0.358515 | 0.225221 | intron-variant | NUB1 | GRCh38.p7 | 7:151351939 | CACTAGTATGTGGCA[A/G]ACGTGTGTGTGTGTG | 51667 |
rs383600 | snp | C/G | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151362273 | ATCTATTTATCCTGG[C/G]CATCTATTTATCCTG | 51667 |
rs386223 | snp | G/T | 0.485731 | 0.0832509 | intron-variant | NUB1 | GRCh38.p7 | 7:151352417 | TTTAATCATGATAGC[G/T]CTTTTATCCATTTTA | 51667 |
rs386956 | snp | C/T | 0.498154 | 0.0303247 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151366978 | CACAGTGGATAACTA[C/T]GCCGTCCTCCAGCTG | 51667 |
rs387859 | snp | C/T | 0.302686 | 0.244385 | intron-variant | NUB1 | GRCh38.p7 | 7:151358472 | tgatctgacaggagg[C/T]ggagctcaggcggtg | 51667 |
rs390052 | snp | C/G | 0.474 | 0.111014 | intron-variant | NUB1 | GRCh38.p7 | 7:151349915 | TTCGGGGCCACTACC[C/G]GTTTCCGCGTCTAGG | 51667 |
rs390370 | snp | A/G | 0.403684 | 0.197183 | intron-variant | NUB1 | GRCh38.p7 | 7:151349810 | GTCTCCGCACATGAG[A/G]AGAAAAACCACAGAC | 51667 |
rs391303 | snp | A/G | 0.480618 | 0.0965156 | intron-variant | NUB1 | GRCh38.p7 | 7:151349563 | AGCCTTCTGTGCTGT[A/G]TCCTCCTGCACAGGC | 51667 |
rs394259 | snp | C/T | 0.211212 | 0.246973 | intron-variant | NUB1 | GRCh38.p7 | 7:151352251 | TGGAGACCACAGTGC[C/T]GTAGATCCATGTGAA | 51667 |
rs400256 | snp | C/G | 0.21695 | 0.247806 | intron-variant | NUB1 | GRCh38.p7 | 7:151348903 | GTGGAGTTTAGAGAG[C/G]CCAGGAAAAAGTGAA | 51667 |
rs404919 | snp | C/T | 0.476918 | 0.104919 | intron-variant | NUB1 | GRCh38.p7 | 7:151350926 | cgcatcagcacttca[C/T]tcctttgcattgtga | 51667 |
rs405166 | snp | C/T | 0.473543 | 0.111932 | intron-variant | NUB1 | GRCh38.p7 | 7:151350861 | ctatcccttcatctg[C/T]tgatggacatttgga | 51667 |
rs405281 | snp | C/T | 0.419616 | 0.183658 | intron-variant | NUB1 | GRCh38.p7 | 7:151365262 | acccaaagcagaggt[C/T]tcatattagaggggt | 51667 |
rs406308 | snp | C/T | 0.221141 | 0.248329 | intron-variant | NUB1 | GRCh38.p7 | 7:151350424 | tgcccggaaaggccc[C/T]cgttacttagcagac | 51667 |
rs406624 | snp | A/T | 0.467234 | 0.12373 | intron-variant | NUB1 | GRCh38.p7 | 7:151361537 | TACTAAGAGACTATG[A/T]TGCAGACATATTCAA | 51667 |
rs408091 | snp | C/T | 0.421051 | 0.182323 | intron-variant | NUB1 | GRCh38.p7 | 7:151347505 | ATCTGTTGCCCAGGC[C/T]GGAGTGCAATGGCAT | 51667 |
rs408503 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362249 | GAGAAAGTTTTTTTT[A/T]TCCTGGGCATCTATT | 51667 |
rs411296 | snp | A/G | 0.216349 | 0.247725 | intron-variant | NUB1 | GRCh38.p7 | 7:151348479 | GAGAATCTTCTAAGG[A/G]GAAGAAAAGGGTGGG | 51667 |
rs414168 | snp | C/T | 0.341235 | 0.232758 | intron-variant | NUB1 | GRCh38.p7 | 7:151349746 | CTGAGAGTGCTGGCA[C/T]CGATCAGTCCCAAGA | 51667 |
rs421635 | snp | C/T | 0.345037 | 0.231231 | intron-variant | NUB1 | GRCh38.p7 | 7:151348936 | CAGTCCACACTGTGG[C/T]TTGACATCTTGAGAG | 51667 |
rs421975 | snp | A/C | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151363215 | acagtcactgtttta[A/C]tgtccttgtctacta | 51667 |
rs423252 | snp | C/T | 0.420733 | 0.18262 | intron-variant | NUB1 | GRCh38.p7 | 7:151355613 | AGGAGATGAAGGCTG[C/T]GGGGAGCCATGATCG | 51667 |
rs429124 | snp | C/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151362805 | tgtgtgtgaggaaac[C/T]gcccagggctgggca | 51667 |
rs431281 | snp | C/G | 0.485324 | 0.0843964 | intron-variant | NUB1 | GRCh38.p7 | 7:151350585 | taggttataattgta[C/G]aacaaagattattgt | 51667 |
rs434705 | snp | C/T | 0.433382 | 0.169915 | intron-variant | NUB1 | GRCh38.p7 | 7:151355061 | TACTGCAGTCTGTCA[C/T]GGTTAAAAGCAAAGA | 51667 |
rs436074 | snp | C/T | 0.282895 | 0.247826 | intron-variant | NUB1 | GRCh38.p7 | 7:151364867 | ttatttaaataaata[C/T]tttacgtttatttta | 51667 |
rs436414 | snp | C/T | 0.264084 | 0.249603 | intron-variant | NUB1 | GRCh38.p7 | 7:151365030 | agagtctctatgttg[C/T]tcaggctggtctcaa | 51667 |
rs438559 | snp | A/G | 0.337158 | 0.234315 | intron-variant | NUB1 | GRCh38.p7 | 7:151346614 | CATACAAACCCCTAA[A/G]TGACAGATTTTGGAC | 51667 |
rs439218 | snp | A/G | 0.340333 | 0.233109 | intron-variant | NUB1 | GRCh38.p7 | 7:151346949 | agggcttttttgtgg[A/G]ctgagcccttaaacc | 51667 |
rs444648 | snp | C/G/T | 0.512477 | 0.167353 | intron-variant | NUB1 | GRCh38.p7 | 7:151352732 | ACAGGCGTGAGCCAC[C/G/T]GGGCCTGGCTAATGT | 51667 |
rs446079 | snp | A/G | 0.46703 | 0.124089 | intron-variant | NUB1 | GRCh38.p7 | 7:151362988 | tagcttttaagcttt[A/G]ttaagtgaaaccaaa | 51667 |
rs446886 | snp | A/G | 0.442162 | 0.159918 | intron-variant | NUB1 | GRCh38.p7 | 7:151355957 | CAAAGAGAGGTACCC[A/G]GAGCTCTGGGCTTGT | 51667 |
rs447776 | snp | C/T | 0.282895 | 0.247826 | intron-variant | NUB1 | GRCh38.p7 | 7:151365093 | ctcacacctgtaatc[C/T]cagcactttgggagg | 51667 |
rs449081 | snp | C/T | 0.394155 | 0.204253 | intron-variant | NUB1 | GRCh38.p7 | 7:151351398 | TAAGACAAAGTAAAA[C/T]GTACTTGAATTTAAC | 51667 |
rs450947 | snp | A/G | 0.493247 | 0.0577133 | intron-variant | NUB1 | GRCh38.p7 | 7:151350056 | gggggcctttccctt[A/G]taggtagacgaggcg | 51667 |
rs451593 | snp | A/G | 0.420574 | 0.182769 | intron-variant | NUB1 | GRCh38.p7 | 7:151355211 | CAGATCAAAGCAACA[A/G]ATATTTGATAATCTA | 51667 |
rs452310 | snp | A/G | 0.315516 | 0.241263 | intron-variant | NUB1 | GRCh38.p7 | 7:151362131 | ccaaatttgtattca[A/G]tggttccctgagacc | 51667 |
rs731995 | snp | A/G | 0.241053 | 0.24984 | intron-variant | NUB1 | GRCh38.p7 | 7:151376007 | CTGCCTGATTCACCC[A/G]GGTTACCCCAAGCAA | 51667 |
rs736469 | snp | C/G | 0.381697 | 0.212499 | intron-variant | NUB1 | GRCh38.p7 | 7:151376572 | CTGCCACCCCCGTCA[C/G]CCATACGAGTGGACA | 51667 |
rs736470 | snp | A/G | 0.030665 | 0.119967 | intron-variant | NUB1 | GRCh38.p7 | 7:151376484 | TCATGCTTCTGTGCA[A/G]TGTGAGCGTAGAGCA | 51667 |
rs874607 | snp | C/T | 0.401924 | 0.198543 | intron-variant | NUB1 | GRCh38.p7 | 7:151367786 | TACTCATCTCTGTCA[C/T]TCCCTTGGTCTCCAG | 51667 |
rs1468510 | snp | C/T | 0.225005 | 0.248747 | intron-variant | NUB1 | GRCh38.p7 | 7:151360599 | ATAATATCACCATTA[C/T]ACAGCTCTTAAACAA | 51667 |
rs1468511 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151353864 | AATTGCTAGAGATGA[C/T]GCTGGAAAGCAAGGC | 51667 |
rs2063995 | snp | A/G | 0.365232 | 0.22186 | intron-variant | NUB1 | GRCh38.p7 | 7:151343308 | TCCCTGTCCTGATTA[A/G]CCTAATTCTTGTCCC | 51667 |
rs2108725 | snp | C/T | 0.458084 | 0.138567 | intron-variant | NUB1 | GRCh38.p7 | 7:151372608 | CACCCCAACCACACA[C/T]GCCAGCAGGAGTCTT | 51667 |
rs2108726 | snp | A/G | 0.47743 | 0.103805 | intron-variant | NUB1 | GRCh38.p7 | 7:151372325 | TAATCATGTAAACAC[A/G]TGTGAGAACATTATT | 51667 |
rs2142172 | snp | C/T | 0.485 | 0.0852928 | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341872 | GGCGGCCGAGTGTCC[C/T]CGACCCCAGCCTCAG | 51667 |
rs2159158 | snp | C/T | 0.499992 | 0.00201604 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151377210 | TTAGTTTTTCTTTGT[C/T]GCTGACTTCCTATTT | 51667 |
rs2240628 | snp | A/G | 0.464523 | 0.128375 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377577 | AGCTGGAGAGGAAGC[A/G]GTCGGGACACCCTTC | 51667 |
rs2240629 | snp | C/G | 0.445196 | 0.1562 | intron-variant | NUB1 | GRCh38.p7 | 7:151376929 | TGTCCAGGTGGCCGG[C/G]CCGGTGACGTCAGGG | 51667 |
rs2302127 | snp | C/T | 0.459233 | 0.136827 | intron-variant | NUB1 | GRCh38.p7 | 7:151374885 | CCCCCTCGGGACCCC[C/T]CACCACGTGTGCTCT | 51667 |
rs2302128 | snp | A/G | 0.4444 | 0.15719 | intron-variant | NUB1 | GRCh38.p7 | 7:151374840 | CTGACCTGCGGGGCC[A/G]AGAGGGCAGAGGGTG | 51667 |
rs2302129 | snp | A/T | 0.399253 | 0.200558 | intron-variant | NUB1 | GRCh38.p7 | 7:151374753 | ATGCTTCTCCAACAC[A/T]GGGAAGGAAGTGGCC | 51667 |
rs2302130 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | NUB1 | GRCh38.p7 | 7:151360061 | GCATATTACTTTTTA[A/G]AAAACAAAGTAAAAA | 51667 |
rs2302131 | snp | C/T | 0.000307131 | 0.0123883 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345387 | TCTTCCCTTAAAAAC[C/T]GGGTCAATTTTGCTT | 51667 |
rs2429249 | snp | C/T | 0.0573587 | 0.15934 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340283 | cacatcaggaaaaag[C/T]ccgttgattgctcag | 51667 |
rs2471918 | snp | A/T | 0.36021 | 0.224397 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341094 | ATATATACACACACT[A/T]CATTTTTCCTATACA | 51667 |
rs2487148 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | NUB1 | GRCh38.p7 | 7:151343092 | GAATCTTCAGAAATT[C/T]TGAATAAAATATCAC | 51667 |
rs2487149 | snp | A/G | 0.350109 | 0.229081 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340035 | AACATCTGTTTGAAG[A/G]CAGTGAAAGCTGCTG | 51667 |
rs2975200 | snp | C/T | 0.457969 | 0.138741 | intron-variant | NUB1 | GRCh38.p7 | 7:151344856 | AATATGAAAATTAGC[C/T]GGGCGTGGTGGCGCA | 51667 |
rs2994483 | snp | A/C | 0.0490535 | 0.14873 | intron-variant | NUB1 | GRCh38.p7 | 7:151344917 | cgccccctgggttca[A/C]gcaattcccctgcat | 51667 |
rs2994484 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NUB1 | GRCh38.p7 | 7:151344776 | ctgacctcaagtgat[C/T]cacccgccttggtct | 51667 |
rs2994485 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | NUB1 | GRCh38.p7 | 7:151344770 | tcaagtgattcaccc[A/G]ccttggtctcaaaac | 51667 |
rs3217033 | in-del | -/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360311 | CAAGGGCATGGCAGG[-/G]TGTTCTGTATAGTCT | 51667 |
rs3748094 | snp | A/G | 0.25045 | 0.25 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378237 | CTCAATCCACTCGGC[A/G]CCTGGCTGCTGCTGT | 51667 |
rs3750177 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341701 | GGCCCCGCCCACAAC[C/T]CTCTTTCCAAGCGGC | 51667 |
rs3834743 | in-del | -/AA | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339803 | CAAGGACAATTGCTG[-/AA]TTCAAGGCTTGTATG | 51667 |
rs3838706 | in-del | -/AC/ACAC/ACACAC/ACACACAC/ACACACACACAC/ACACACACACACAC | 0.625 | 0.125 | intron-variant | NUB1 | GRCh38.p7 | 7:151351936 | CACACACACACACAC[lengthTooLong]GTTTGCCACATACTA | 51667 |
rs4295576 | snp | C/T | 0.46754 | 0.123192 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341248 | GCAGAGCTCCCTAGG[C/T]CTTGTGGTCCCTAGT | 51667 |
rs4430016 | snp | A/G | 0.499741 | 0.0113788 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341169 | GAGATTAACAGCAAT[A/G]ACTGATAATAAAATA | 51667 |
rs4726017 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUB1 | GRCh38.p7 | 7:151368439 | gggtgagaaatgCCA[C/T]GTGCACAGCTGAAAT | 51667 |
rs4726018 | snp | A/G | 0.264358 | 0.249587 | intron-variant | NUB1 | GRCh38.p7 | 7:151374978 | CGGCGGGCAGGAAGC[A/G]GAGTGGTAGGAGCTG | 51667 |
rs5888438 | snp | G/T | 0.116465 | 0.211349 | intron-variant | NUB1 | GRCh38.p7 | 7:151356721 | GTGGGttttttgttt[G/T]tttttttgtttttga | 51667 |
rs6464138 | snp | C/T | 0.413748 | 0.188909 | intron-variant | NUB1 | GRCh38.p7 | 7:151344868 | agccgggcgtggtgg[C/T]gcatgcctgtaatcc | 51667 |
rs6464139 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | NUB1 | GRCh38.p7 | 7:151344872 | gggcgtggtggcgca[C/T]gcctgtaatcccagt | 51667 |
rs6952675 | snp | A/G | 0.464203 | 0.128908 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377393 | CCAGGGCCTTCATGC[A/G]TGGTCTCGGGGAAGA | 51667 |
rs6957858 | snp | C/T | 0.260227 | 0.249791 | intron-variant | NUB1 | GRCh38.p7 | 7:151371176 | TGTTAGTTACGATGC[C/T]TTTGGCTGAAAGCAA | 51667 |
rs6963048 | snp | A/G | 0.26818 | 0.249338 | intron-variant | NUB1 | GRCh38.p7 | 7:151372210 | CTCTCTTGAGATCTG[A/G]TTCTACTTAACTGTA | 51667 |
rs6979482 | snp | C/T | 0.263809 | 0.249618 | intron-variant | NUB1 | GRCh38.p7 | 7:151375254 | GAATATCATCTAGTT[C/T]GTTTTTTTGTGTGTT | 51667 |
rs7341445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342638 | GACTTAAAATATGTC[A/G]CCACTTACTCTGTTG | 51667 |
rs7341490 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344597 | gctggggttacaggc[C/T]tgagccaccacaccc | 51667 |
rs7457211 | snp | G/T | 0 | 0 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340223 | GCCCTCAGAAAAAAA[G/T]GTCAGAACAGTTTCT | 51667 |
rs7782047 | snp | G/T | 0.471004 | 0.116864 | intron-variant | NUB1 | GRCh38.p7 | 7:151360907 | ctctcaaagtgctgg[G/T]attacaggtgtgagt | 51667 |
rs7798855 | snp | A/G | 0.309894 | 0.242719 | intron-variant | NUB1 | GRCh38.p7 | 7:151360848 | cactatgttgcccat[A/G]ctagtctcaaactcc | 51667 |
rs7805834 | snp | G/T | 0.269267 | 0.249256 | intron-variant | NUB1 | GRCh38.p7 | 7:151346186 | TGATGTGCTTGGGAG[G/T]TGACAAACTGTATTA | 51667 |
rs7809933 | snp | A/G | 0.078151 | 0.181571 | intron-variant | NUB1 | GRCh38.p7 | 7:151352537 | caacctcaaactcgc[A/G]gttcaagcaatcctc | 51667 |
rs9771208 | snp | C/T | 0.370365 | 0.219117 | intron-variant | NUB1 | GRCh38.p7 | 7:151359367 | agaatggtgtgaacc[C/T]gggaggtggagcttg | 51667 |
rs10085614 | snp | C/T | 0.38555 | 0.210062 | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341935 | ACTGGGCACCTCTCC[C/T]GGCCAGGGGTGGAGC | 51667 |
rs10224319 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364161 | ggcgcggtggctcac[A/G]cctgtaatcccaaca | 51667 |
rs10228228 | snp | C/G | 0.413416 | 0.189196 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340876 | gtgctccaacgagct[C/G]ggcagaggaggtggg | 51667 |
rs10238749 | snp | A/G | 0.0123036 | 0.0774623 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378406 | TCATTCTTTTTAAAC[A/G]GATGATACCGATGGA | 51667 |
rs10240455 | snp | C/T | 0.00477324 | 0.0486193 | intron-variant | NUB1 | GRCh38.p7 | 7:151343856 | CAGGGCCCTAATTTT[C/T]TCAGCTGTAAAATGA | 51667 |
rs10244314 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344583 | cagcctcccaaagtg[C/G]tggggttacaggcct | 51667 |
rs10245837 | snp | A/C | 0.270351 | 0.24917 | intron-variant | NUB1 | GRCh38.p7 | 7:151362707 | gaggccaaggaggtg[A/C]gaggagcaagctgcc | 51667 |
rs10252799 | snp | G/T | 0.274124 | 0.248833 | intron-variant | NUB1 | GRCh38.p7 | 7:151346584 | GATTTAATCAGGCCT[G/T]CATAATGAAACTTCC | 51667 |
rs10253388 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364174 | acgcctgtaatccca[A/G]cactatgggaggccg | 51667 |
rs10253396 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364179 | tgtaatcccaacact[A/T]tgggaggccgaggca | 51667 |
rs10256728 | snp | A/T | 0.45946 | 0.136478 | intron-variant | NUB1 | GRCh38.p7 | 7:151370503 | CCACTACCAGTAAGA[A/T]TTTATTATTTTTATT | 51667 |
rs10257799 | snp | A/G | 0.136166 | 0.22258 | intron-variant | NUB1 | GRCh38.p7 | 7:151357910 | ccactgcgcccggcc[A/G]GATTAAAGTTGTTTT | 51667 |
rs10262761 | snp | C/T | 0.144969 | 0.226867 | intron-variant | NUB1 | GRCh38.p7 | 7:151359725 | gaggttgcagtgacc[C/T]gagatcgcaccactg | 51667 |
rs10262974 | snp | A/G | 0.258565 | 0.249853 | intron-variant | NUB1 | GRCh38.p7 | 7:151359772 | ACAGAATGAGACTCC[A/G]TCTCAAAAAAATAAA | 51667 |
rs10263820 | snp | A/C | 0.16846 | 0.236329 | intron-variant | NUB1 | GRCh38.p7 | 7:151347490 | TGAGACAAGGTCTTG[A/C]TCTGTTGCCCAGGCT | 51667 |
rs10275580 | snp | C/T | 0.258843 | 0.249844 | intron-variant | NUB1 | GRCh38.p7 | 7:151362855 | cagggaataatcctc[C/T]gagttcatagaaggc | 51667 |
rs10281126 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | NUB1 | GRCh38.p7 | 7:151351863 | TATTAATAGCTTGCT[A/G]TGACCTTCAGCACGG | 51667 |
rs10571761 | in-del | -/AAAG | 0.238473 | 0.249734 | intron-variant | NUB1 | GRCh38.p7 | 7:151366520 | GGATCAATGATTCTT[-/AAAG]AAAGAAAGAAAGAAA | 51667 |
rs11354135 | in-del | -/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151365332 | TCTTTTTTTTTTTTT[-/T]GGCTGCACAAATAAA | 51667 |
rs11414801 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365890 | AGTCCTTTTTTTTTT[-/T]ATTCCATGCATATTT | 51667 |
rs11550343 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378241 | GGCACTCAATCCACT[C/T]GGCACCTGGCTGCTG | 51667 |
rs11765772 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | NUB1 | GRCh38.p7 | 7:151344928 | ttgcttgaacccagg[A/G]ggcggagcttgcagt | 51667 |
rs11771465 | snp | A/C | 0.184838 | 0.241358 | intron-variant | NUB1 | GRCh38.p7 | 7:151356547 | TATTTTACTAGAGAA[A/C]CTTGTCCCCTAAGGG | 51667 |
rs11772616 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | NUB1 | GRCh38.p7 | 7:151344925 | gaattgcttgaaccc[A/G]gggggcggagcttgc | 51667 |
rs11970791 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | NUB1 | GRCh38.p7 | 7:151364051 | cgtccgcctcagcct[A/C]ccaaagtgctgggat | 51667 |
rs11972311 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | NUB1 | GRCh38.p7 | 7:151353666 | tgtttgtgttttaga[A/G]aggtcacgcagtagg | 51667 |
rs11972709 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | NUB1 | GRCh38.p7 | 7:151371836 | gcaaccttgatctcc[C/T]gggctccaatgatcc | 51667 |
rs11973188 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | NUB1 | GRCh38.p7 | 7:151346901 | gtatgggtaacctgg[A/G]gaccagatacttggt | 51667 |
rs11973759 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | NUB1 | GRCh38.p7 | 7:151372773 | GGAATGACGGAGCCT[A/G]CTGCCCTGTGCAGCG | 51667 |
rs11979062 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | NUB1 | GRCh38.p7 | 7:151353197 | AGGAGAAGAGCTAAG[C/G]CTGTGTCAGGACAGT | 51667 |
rs11980868 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NUB1 | GRCh38.p7 | 7:151351830 | TTAGTTTTGAATTAC[C/T]ATTTTTTTTCCCTAA | 51667 |
rs12667467 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NUB1 | GRCh38.p7 | 7:151347271 | gctggacacagtggc[A/G]catgcctgtagtccc | 51667 |
rs12668261 | snp | C/T | 0.461813 | 0.132798 | intron-variant | NUB1 | GRCh38.p7 | 7:151373445 | AGAACCCTCTGCAGC[C/T]GTCCTGCGCTCCTGC | 51667 |
rs12670537 | snp | C/T | 0.464947 | 0.127663 | intron-variant | NUB1 | GRCh38.p7 | 7:151373207 | TGGGGCTGGTCTCCC[C/T]GGGAGAATGTAGCAA | 51667 |
rs12703118 | snp | A/G | 0.202035 | 0.245356 | intron-variant | NUB1 | GRCh38.p7 | 7:151345197 | ATATATTTTTAGAGA[A/G]GTCTGGAGCTCATTT | 51667 |
rs12703119 | snp | A/G | 0.487871 | 0.076925 | intron-variant | NUB1 | GRCh38.p7 | 7:151358013 | gcggagtctcgctct[A/G]tcatcaggctagagt | 51667 |
rs12703120 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360880 | gggctcaagtgatcc[A/T]cccaccacagcctct | 51667 |
rs12703121 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360887 | agtgatccacccacc[A/T]cagcctctcaaagtg | 51667 |
rs12703122 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360910 | tcaaagtgctggtat[C/T]acaggtgtgagtcgc | 51667 |
rs12703123 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | NUB1 | GRCh38.p7 | 7:151361039 | tcctgccttggcctc[C/T]caaagtgctgggatt | 51667 |
rs13221923 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151357494 | AGAAAGGGTTCAGTA[A/G]CTTCTTATAATGAAT | 51667 |
rs13221961 | snp | C/T | 0.222333 | 0.248464 | intron-variant | NUB1 | GRCh38.p7 | 7:151357672 | tggagtgcagtggtg[C/T]gatctcagctcactg | 51667 |
rs13226693 | snp | C/T | 0.219648 | 0.248151 | intron-variant | NUB1 | GRCh38.p7 | 7:151353528 | CAACAAAGACTTGTC[C/T]AGTCCCAGATGTCAG | 51667 |
rs13232233 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151342802 | TTCGTCCTTCTGTCA[A/G]GTGGTGGCTTGGATG | 51667 |
rs13234689 | snp | C/T | 0.462582 | 0.131564 | intron-variant | NUB1 | GRCh38.p7 | 7:151369455 | AAAACAAAATTGTTT[C/T]TTCATGAGGTCATTA | 51667 |
rs13239160 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344181 | gtgagactccctctc[A/C]aaaaaaaaaaaaaaa | 51667 |
rs13241175 | snp | A/G | 0.150333 | 0.229274 | intron-variant | NUB1 | GRCh38.p7 | 7:151362803 | catgtgtgtgaggaa[A/G]ctgcccagggctggg | 51667 |
rs13308382 | snp | C/G | 0.365646 | 0.221644 | intron-variant | NUB1 | GRCh38.p7 | 7:151370692 | AAGCTATCCCTCCCC[C/G]CTCCCCCCACCCCAC | 51667 |
rs17173091 | snp | C/T | 0.139564 | 0.224285 | intron-variant | NUB1 | GRCh38.p7 | 7:151343567 | TTACTTATTGCTTGT[C/T]TGATTTGGGAAACCT | 51667 |
rs17173096 | snp | C/T | 0.131723 | 0.220251 | intron-variant | NUB1 | GRCh38.p7 | 7:151346135 | AGGGACTAAGGATTG[C/T]CATGAGGCATTAAAT | 51667 |
rs17173099 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | NUB1 | GRCh38.p7 | 7:151354397 | AATGTTAGAAAGGTT[A/G]TCATATTTCTCAAAA | 51667 |
rs17173101 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | NUB1 | GRCh38.p7 | 7:151354524 | TTACCCTTTTTTATT[C/T]TGTTTATTTGCATCT | 51667 |
rs17173104 | snp | A/G | 0.00306431 | 0.0390226 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151355811 | TCACAATGTGAAAGC[A/G]ATGGTGCTTGAACTA | 51667 |
rs17633293 | snp | G/T | 0.0685596 | 0.171987 | intron-variant | NUB1 | GRCh38.p7 | 7:151356458 | CCTGGAGCAGTGACT[G/T]TCAACATACCTGAGG | 51667 |
rs28578868 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347613 | CAGGTGCATGCCACC[A/G]TGCCTGGCTAATATA | 51667 |
rs28589754 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151347847 | CACCATAATTTTTAC[A/G]TACTACATGGTATTA | 51667 |
rs28635585 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151346087 | CTTCTCTGCTCTCAT[A/T]CAGAGTATCCTGAAC | 51667 |
rs28668325 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | NUB1 | GRCh38.p7 | 7:151367646 | AGGCTGGTGCCCTGA[C/T]ACTGACTCTCCTGTG | 51667 |
rs28673382 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346308 | CAGTCTCTTGGTTTA[A/G]AAACTAGGTGTGGCA | 51667 |
rs34033768 | in-del | -/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360432 | TTGACCTTTCCTCCC[-/C]TGTAAAGAAAAGAAT | 51667 |
rs34302976 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353982 | CAGAAACCTTGATTT[-/T]GATGTCATCAAATCC | 51667 |
rs34455667 | in-del | -/A | 0.387642 | 0.208697 | intron-variant | NUB1 | GRCh38.p7 | 7:151363454 | AACAGAGAAAAGGCT[-/A]AAAAAAAAAAAAAAT | 51667 |
rs34462165 | in-del | -/T | | | frameshift-variant | NUB1 | GRCh38.p7 | 7:151367904 | TCTAAGACTCTACTT[-/T]ACTTCAAGGGATCCG | 51667 |
rs34622454 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359484 | AATGAATGCCCTTTT[-/T]AAAGATACAAGCAGC | 51667 |
rs35044604 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362216 | ATGAAATAATAATTA[A/C]CAATGTCTTTCTAAG | 51667 |
rs35143418 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151361737 | AGTCCCAACTTTAAC[-/T]GTACACAAAAAAGGA | 51667 |
rs35146376 | in-del | -/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368725 | ATTCTTACATTTCCC[-/C]TGTCTCTAGGCACGT | 51667 |
rs35218575 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342854 | ATTTGTTTATTTTTT[-/T]AGTAGAGACGGGGTT | 51667 |
rs35231514 | in-del | -/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370597 | TGCACAATGTGCAGG[-/G]TTAGTTACATATGTA | 51667 |
rs35366827 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367607 | CTCTGCTGACCAGAA[-/A]GGGCCACTGTGCTGC | 51667 |
rs35542644 | snp | G/T | 0.222928 | 0.24853 | intron-variant | NUB1 | GRCh38.p7 | 7:151362648 | GCAAACCCAGGCAGA[G/T]CCTTGTGCTCCCTGG | 51667 |
rs35621343 | in-del | -/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376916 | TGAGGGGGCGTCCCC[-/C]TGACGTCACCGGCCC | 51667 |
rs35886370 | snp | C/T | 0.22263 | 0.248497 | intron-variant | NUB1 | GRCh38.p7 | 7:151359911 | ATGAAAGCAAAGGGC[C/T]AAGTGCTGGTTAGGA | 51667 |
rs35944435 | in-del | -/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368952 | AGATAATCCCACAGG[-/G]AGTGTTAATAACCAG | 51667 |
rs35993758 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360506 | TGTTGCTAGTCGGAA[-/A]CTTTCCATTATAAAG | 51667 |
rs56174188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151371758 | TTCGTTCATGTTTTT[A/G]TTTGAGACAGAGCCT | 51667 |
rs57035345 | in-del | -/TTAG | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363759 | CTTTCTTGAAAAAAG[-/TTAG]GTAAGTTTGGCTTAT | 51667 |
rs57088077 | snp | A/C/T | 0.00517822 | 0.0506191 | intron-variant | NUB1 | GRCh38.p7 | 7:151365905 | CTTTTTTTTTTATTC[A/C/T]ATGCATATTTTGATA | 51667 |
rs57277870 | in-del | -/CTGA | 0.0217236 | 0.101931 | intron-variant | NUB1 | GRCh38.p7 | 7:151375793 | GGGTGCAGCGCCTGT[-/CTGA]ATGTGTGAAGAGTTC | 51667 |
rs57382814 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NUB1 | GRCh38.p7 | 7:151376576 | CACTCGTATGGCTGA[C/T]GGGGGTGGCAGAAGA | 51667 |
rs57489077 | in-del | -/C | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151371364 | TTACCCCCACCCCCC[-/C]ACCCCATGTCATCAG | 51667 |
rs57738370 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | NUB1 | GRCh38.p7 | 7:151344943 | GGGCGGAGCTTGCAG[C/T]GAGCCGAGATCGCAC | 51667 |
rs57934390 | snp | C/G | 0.040671 | 0.13668 | intron-variant | NUB1 | GRCh38.p7 | 7:151368127 | TATTTGTATATGTTA[C/G]AGTACAGCCAGATGC | 51667 |
rs58078152 | in-del | -/A | 0.375 | 0.216506 | intron-variant | NUB1 | GRCh38.p7 | 7:151347418 | TAAAAGAAAAAAAAA[-/A]GTATATATAGGTTTA | 51667 |
rs58113312 | in-del | -/T | 0.311637 | 0.242283 | intron-variant | NUB1 | GRCh38.p7 | 7:151365891 | ACAAAATTAAAGTCC[-/T]TTTTTTTTTATTCCA | 51667 |
rs58156271 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | NUB1 | GRCh38.p7 | 7:151359769 | ACGACAGAATGAGAC[-/T]CCGTCTCAAAAAAAT | 51667 |
rs58312475 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354682 | GGAAACTGAGTCCTA[A/G]AAGATAGGTAGTTTA | 51667 |
rs59119243 | in-del | -/TTT | 0.422158 | 0.181278 | intron-variant | NUB1 | GRCh38.p7 | 7:151357201 | TTTTTTTTTTTTTTT[-/TTT]GAGATGGAGTCTCGC | 51667 |
rs59356301 | snp | C/G | 0.00716266 | 0.059414 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341364 | GGGTGAAAAGCCGCT[C/G]GTTTAGGGAAGGGGT | 51667 |
rs59555540 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359293 | ATACAAAAAAAAAAA[-/A]TTAGCCAGGCGTGGT | 51667 |
rs59584074 | snp | C/G | 0.137187 | 0.223099 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377803 | AGGTCGCAGCAAATG[C/G]CTTCAGCCTGGGACG | 51667 |
rs59705983 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359449 | TCTGTCTCAAAAAAA[-/A]AAAAAAGAATAGAAA | 51667 |
rs59781719 | in-del | -/TTTTT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348589 | TTTTTTTTTTTTTTT[-/TTTTT]GAGGCGGAGTCTTGC | 51667 |
rs60175285 | snp | A/C | 0.122411 | 0.214991 | intron-variant | NUB1 | GRCh38.p7 | 7:151365078 | ATTTTCCTGCCTCGG[A/C]CTCCCAAAGTGCTGA | 51667 |
rs60437024 | in-del | -/TC/TCACACAC | 0.0326441 | 0.123517 | intron-variant | NUB1 | GRCh38.p7 | 7:151351916 | TGGCCCATCTGTAAA[-/TC/TCACACAC]ACACACACACACACA | 51667 |
rs60655814 | snp | C/T | 0.251296 | 0.249997 | intron-variant | NUB1 | GRCh38.p7 | 7:151362446 | CTTCTCCAAGTAAGC[C/T]AGAAGTTTTGTCACA | 51667 |
rs60855391 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | NUB1 | GRCh38.p7 | 7:151365210 | TTTTATATATAATAA[G/T]AAGTGTTGATTTCTC | 51667 |
rs61612466 | snp | A/C | 0.0490535 | 0.14873 | intron-variant | NUB1 | GRCh38.p7 | 7:151376438 | GCTCCCTGACGCACC[A/C]GACTTGAGTCTTCCA | 51667 |
rs61638536 | snp | A/C | 0.126909 | 0.217598 | intron-variant | NUB1 | GRCh38.p7 | 7:151347752 | GCATGAGCCATCGCG[A/C]CCAATCTATACTCAT | 51667 |
rs61734185 | snp | G/T | 0.0159058 | 0.087749 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345361 | AGGGATGGCACAAAA[G/T]AAATATCTTCAAGCA | 51667 |
rs61734186 | snp | A/C/G | 0.000149688 | 0.00865004 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349238 | CCACCAAGACTAAAA[A/C/G]AAGTGAGTAATTTCC | 51667 |
rs61756130 | snp | A/G | 0.00168312 | 0.0289608 | missense | NUB1 | GRCh38.p7 | 7:151367016 | TGTGGTGTTACTTCC[A/G]CCTGGAACAGCTGGA | 51667 |
rs62490271 | snp | C/G | 0.16911 | 0.236552 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340966 | ACTGCAAGGTTACAG[C/G]AGTCCCCTCTCGTCC | 51667 |
rs62490272 | snp | C/T | 0.170733 | 0.237101 | intron-variant | NUB1 | GRCh38.p7 | 7:151342093 | CAGAGGTGTGGGGTA[C/T]TTAAAAGAAAATATT | 51667 |
rs62490273 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344366 | CCCAGGCTGGAGTGC[A/G]GTGGTGCCATCTCGG | 51667 |
rs62490274 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | NUB1 | GRCh38.p7 | 7:151347749 | CAGGCATGAGCCATC[A/G]CGCCCAATCTATACT | 51667 |
rs62490275 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348968 | AGTGTAACGGGGCGA[C/T]CTCCACTCATCAGAG | 51667 |
rs62490276 | snp | A/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151351764 | CTTGGTGCATGTTTG[A/T]GTGAATGAGTGAGTG | 51667 |
rs62490277 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354339 | TTTTTTTTTTTTTTA[A/T]TCAAGATGGCTTAAC | 51667 |
rs62490278 | snp | A/G | 0.327211 | 0.237778 | intron-variant | NUB1 | GRCh38.p7 | 7:151364290 | GCCGGGCATGGTGGC[A/G]GGCGCCTGTAGTCCC | 51667 |
rs62490279 | snp | A/C | 0.295854 | 0.245759 | intron-variant | NUB1 | GRCh38.p7 | 7:151364481 | AAGACAAACATAATA[A/C]ATTTCTGTTAAATAA | 51667 |
rs62490280 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NUB1 | GRCh38.p7 | 7:151366404 | GTCTTTAAAGAAGTG[C/G]TGTTCAGCCCTGGCT | 51667 |
rs66519748 | snp | A/C | 0.184521 | 0.241273 | intron-variant | NUB1 | GRCh38.p7 | 7:151353722 | TTGACTTGGGGAGAC[A/C]AGTTAGCTACTGCAG | 51667 |
rs67573855 | in-del | -/A | 0.410933 | 0.191313 | intron-variant | NUB1 | GRCh38.p7 | 7:151356722 | CTCAAAAACAAAAAA[-/A]CAAACAAAAAACCCA | 51667 |
rs67653640 | in-del | -/GAAA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151366531 | TCTTAAAGAAAGAAA[-/GAAA]GAAAGAAAGAACGTT | 51667 |
rs67774209 | in-del | -/T | 0.344592 | 0.231414 | intron-variant | NUB1 | GRCh38.p7 | 7:151365319 | GTTTTCTTCTCTCTC[-/T]TTTTTTTTTTTTTGG | 51667 |
rs67778727 | in-del | -/ATAAAA | 0.00953873 | 0.0683987 | intron-variant | NUB1 | GRCh38.p7 | 7:151361972 | AAATTTCAAATAGTC[-/ATAAAA]ATAAAAATTAGTATA | 51667 |
rs71198709 | in-del | -/AAAA | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151348570 | GCAAGACTCCGCCTC[-/AAAA]AAAAAAAAAAAAAAA | 51667 |
rs71198710 | in-del | -/CCAGCACTTTGGGAGGCCAAGGCAGGAGGATCACATGAGTCCAGGAGTTCAAGATCAGCCTGAGCAACACAGGGAGACCCCATCTGTATAATTAAAAAAAAAAAAAAAAAAAAAAAGCCGACACAGCGACTCACACCTGTAATA | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151360907 | CTCACACCTGTAATC[lengthTooLong]CCAGCACTTTGAGAG | 51667 |
rs71531422 | multinucleotide-polymorphism | AGT/GGG | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151352700 | TAATCCCAACACCCT[AGT/GGG]AGGCCAAGGTGGGAG | 51667 |
rs71533531 | in-del | -/A | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151359705 | CGCTTGAACCCAGGA[-/A]GGCAGAGGTTGCAGT | 51667 |
rs71539874 | snp | A/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151345480 | AGGTATTTTTCTTTT[A/T]AGACATCAATAATTA | 51667 |
rs71539875 | snp | A/C | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151359808 | TAAAATAAAAATGAT[A/C]CAAGCATTACTGGCT | 51667 |
rs71539876 | snp | A/G | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378691 | TCAGGGTTTGCCTCA[A/G]AAGTGCCTGGTGAGC | 51667 |
rs72617364 | snp | A/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151351917 | TGGCCCATCTGTAAA[A/T]CACACACACACACAC | 51667 |
rs73171842 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | NUB1 | GRCh38.p7 | 7:151365714 | GTGCACACGTGTGTA[A/G]AACATGGTGTATGTG | 51667 |
rs73472479 | snp | C/T | 0.131723 | 0.220251 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341305 | TTCCCGGGAAGCAGC[C/T]TAATTTCACCCCAGG | 51667 |
rs73472482 | snp | A/G | 0.121369 | 0.214369 | intron-variant | NUB1 | GRCh38.p7 | 7:151343348 | ATAAAATAGATTTGA[A/G]CTTTCTTTTAAAAAA | 51667 |
rs73472483 | snp | A/G | 0.104149 | 0.203046 | intron-variant | NUB1 | GRCh38.p7 | 7:151343879 | TAAAATGATCCGATC[A/G]GTGTTAGATTTGAAT | 51667 |
rs73472490 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | NUB1 | GRCh38.p7 | 7:151346643 | ACAGCTTCCAAATTG[G/T]TGAACACATCCACAT | 51667 |
rs73472494 | snp | A/T | 0.130008 | 0.219321 | intron-variant | NUB1 | GRCh38.p7 | 7:151347943 | TTTAATGAAACATTA[A/T]CCTCACATGCAGATA | 51667 |
rs73472502 | snp | A/G | 0.100464 | 0.200366 | intron-variant | NUB1 | GRCh38.p7 | 7:151352897 | GGTATGTATGGCAAA[A/G]TATGCATAATTTTTT | 51667 |
rs73474411 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | NUB1 | GRCh38.p7 | 7:151361645 | TGCATTCCCAAGATA[A/C]TACTGTATACTCCCA | 51667 |
rs73727157 | snp | A/G | 0.104504 | 0.2033 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378623 | GCTGTGAAAGATGCC[A/G]CACGCCAAGCGGGGC | 51667 |
rs74344235 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | NUB1 | GRCh38.p7 | 7:151362517 | CCAAGAATAGTTTCT[C/T]TCCCCAAATTGTATG | 51667 |
rs74366631 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | NUB1 | GRCh38.p7 | 7:151365669 | TTTGGAGAAAGCACC[C/T]CTCACCCAGCTCCAC | 51667 |
rs74375578 | snp | A/C | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151364440 | ACAAAAACAAAAAAA[A/C]ACAAAAAAAAAAACA | 51667 |
rs74576652 | snp | A/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151354337 | CTTTTTTTTTTTTTT[A/T]AATCAAGATGGCTTA | 51667 |
rs74644100 | snp | C/G/T | 0.0310518 | 0.120672 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377400 | CTTCATGCGTGGTCT[C/G/T]GGGGAAGAAGCTTCC | 51667 |
rs74778987 | snp | C/T | 0.169435 | 0.236663 | intron-variant | NUB1 | GRCh38.p7 | 7:151343566 | TTTACTTATTGCTTG[C/T]CTGATTTGGGAAACC | 51667 |
rs75024525 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | NUB1 | GRCh38.p7 | 7:151372221 | TCTGATTCTACTTAA[A/C]TGTAGCCACTTCAGT | 51667 |
rs75066556 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151353776 | CACTGGTTTCCAGTG[A/C]GTTCCTGTGGCCTCG | 51667 |
rs75250543 | snp | A/C | 0.0869089 | 0.189476 | intron-variant | NUB1 | GRCh38.p7 | 7:151353147 | ATGTAAGGTGTGCTG[A/C]GTGTAAGATGCCAGT | 51667 |
rs75351392 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151374558 | ACAGGCAGTTTCCAC[A/G]GCAGAAAAAAGAGAA | 51667 |
rs75507823 | snp | C/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151365891 | ACAAAATTAAAGTCC[C/T]TTTTTTTTTATTCCA | 51667 |
rs75564057 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358447 | AGGTGAGCAGCAGGC[A/T]AGTGAGCGTCACCGC | 51667 |
rs75578141 | snp | C/T | 0.0918018 | 0.19358 | intron-variant | NUB1 | GRCh38.p7 | 7:151356118 | GGAGGTCCTTTTGGT[C/T]TTGTTACAGCAGCAG | 51667 |
rs75830221 | snp | C/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151365889 | TGACAAAATTAAAGT[C/T]CTTTTTTTTTTATTC | 51667 |
rs75833506 | snp | A/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151344489 | CTAATTGTTCATATA[A/T]TTTTTTTTTTTTAGT | 51667 |
rs75857504 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | NUB1 | GRCh38.p7 | 7:151357083 | GTACAGTGGCACCAT[C/T]ATAGCTCACTGCAGC | 51667 |
rs75978730 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | NUB1 | GRCh38.p7 | 7:151366478 | AGGCCCAACCCCCAG[A/G]AATTTCTGTTATGTT | 51667 |
rs75996270 | snp | A/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151363469 | AAAAAAAAAAAAAAA[A/T]GAACAGAGCATCTGC | 51667 |
rs76042785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151361563 | TTCAACATTTGAAAA[A/G]TAGACTTGATTTTTT | 51667 |
rs76192630 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365901 | AGTCCTTTTTTTTTT[A/T]TTCCATGCATATTTT | 51667 |
rs76360473 | snp | G/T | 0.0883596 | 0.190715 | intron-variant | NUB1 | GRCh38.p7 | 7:151350412 | CGCTAGACCAAGGTC[G/T]GCTAAGTAACGAGGG | 51667 |
rs76396283 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | NUB1 | GRCh38.p7 | 7:151350459 | AGTTACCGCTAGACG[A/G]GGGAGCCCTCTAGTG | 51667 |
rs76423975 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | NUB1 | GRCh38.p7 | 7:151354719 | GCCACAGAGTTAAAA[C/T]GGTAGATGGAGCCCA | 51667 |
rs76462484 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | NUB1 | GRCh38.p7 | 7:151372043 | AGTTTATATTTTTTG[A/T]GCAATATGGCCCTGA | 51667 |
rs76537721 | snp | A/C | 0.245916 | 0.249967 | intron-variant | NUB1 | GRCh38.p7 | 7:151364453 | AAAACAAAAAAAAAA[A/C]CAAAAAAACTGTAAG | 51667 |
rs76551060 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NUB1 | GRCh38.p7 | 7:151346242 | GTTCCAGGCAGGCCT[C/T]ACTTTTTCTTTGCAA | 51667 |
rs76559162 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346826 | GTTGTTCTAGCAAAT[C/T]ATGGAACCTGAAGGG | 51667 |
rs76595089 | in-del | -/ACACA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351919 | CCCATCTGTAAAACA[-/ACACA]CACACACACACACAC | 51667 |
rs76597309 | snp | A/T | 0.078151 | 0.181571 | intron-variant | NUB1 | GRCh38.p7 | 7:151352443 | TTAAAGCCTTCTTTT[A/T]AAAAATATTTATTTT | 51667 |
rs76859081 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | NUB1 | GRCh38.p7 | 7:151351367 | CTGATTTCACAGGGT[A/T]ATCTCTCCAAAATGG | 51667 |
rs77063105 | snp | A/C | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151364442 | AAAAACAAAAAAAAA[A/C]AAAAAAAAAAACAAA | 51667 |
rs77138934 | snp | A/C | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151352700 | CTCCCACCTTGGCCT[A/C]CCAGGGTGTTGGGAT | 51667 |
rs77203392 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | NUB1 | GRCh38.p7 | 7:151366547 | AAAGAAAGAAAGAAC[A/G]TTGCTCTGGCCCAGG | 51667 |
rs77294339 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NUB1 | GRCh38.p7 | 7:151373702 | GAAGGCCTTCCCACC[A/G]CGTGCAGAAGCTCTC | 51667 |
rs77300744 | snp | A/G | 0.0130921 | 0.0798413 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377657 | CTTCCTGCTTCCCAC[A/G]CTGCCATCTCTGCCA | 51667 |
rs77529903 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NUB1 | GRCh38.p7 | 7:151372926 | CCAGGAGGTTCTCCT[A/G]TGATAGAGACAGGCC | 51667 |
rs77551693 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NUB1 | GRCh38.p7 | 7:151352293 | AACAAGCAGTAAAAC[A/G]GAAAGTTTAAAAAGG | 51667 |
rs77693954 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | NUB1 | GRCh38.p7 | 7:151376578 | CTCGTATGGCTGACG[A/G]GGGTGGCAGAAGAGG | 51667 |
rs77721119 | snp | C/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151352702 | CCCACCTTGGCCTCC[C/T]AGGGTGTTGGGATTA | 51667 |
rs77761377 | snp | C/G | 0.139225 | 0.224118 | intron-variant | NUB1 | GRCh38.p7 | 7:151343600 | AAGCGCTGTGCTACA[C/G]CTGCCAGCTGCCTTA | 51667 |
rs77830669 | snp | A/C | | | missense | NUB1 | GRCh38.p7 | 7:151356209 | CAATCAGAATTCCCC[A/C]ATCAGAAAGAAAAGT | 51667 |
rs77860613 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NUB1 | GRCh38.p7 | 7:151371843 | TGATCTCCCGGGCTC[C/T]AATGATCCTCCTGCC | 51667 |
rs77891615 | snp | A/G | 0.0558544 | 0.157504 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340995 | CCACACACAGGTGGT[A/G]TGTCCCAAGACCCAC | 51667 |
rs78632072 | in-del | -/TG | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348170 | CATCTGGATTTTTTT[-/TG]GGGGAGGAACCATAA | 51667 |
rs78640108 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | NUB1 | GRCh38.p7 | 7:151372243 | CACTTCAGTGCAGTA[C/T]TCACTGTCATTGATT | 51667 |
rs78649226 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350410 | ACCGCTAGACCAAGG[C/T]CTGCTAAGTAACSRG | 51667 |
rs78669217 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUB1 | GRCh38.p7 | 7:151368590 | TTTGTACTTGTTAAT[A/G]ACAGGCCTAGTTTAG | 51667 |
rs78684465 | snp | C/T | | | missense | NUB1 | GRCh38.p7 | 7:151376778 | CCAGAAGACTCTTTG[C/T]CCCCGCCAGCCACGT | 51667 |
rs78815323 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NUB1 | GRCh38.p7 | 7:151375755 | AGCAGCAGAGGACGG[C/T]GGGGTCTGCCTAGCA | 51667 |
rs79418595 | snp | A/C | 0.0763149 | 0.179815 | intron-variant | NUB1 | GRCh38.p7 | 7:151374652 | ATTTATTTAGTCCAT[A/C]GTACATGTTGGCAAA | 51667 |
rs79550186 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | NUB1 | GRCh38.p7 | 7:151362404 | TCAGTTTTTCCATTT[A/C]CTTTTCCATTTGACT | 51667 |
rs79560277 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NUB1 | GRCh38.p7 | 7:151348237 | TCTTGAGCCCTTTCA[A/G]TCTTCTTTTTTTTCT | 51667 |
rs79597895 | snp | A/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151363467 | CTAAAAAAAAAAAAA[A/T]ATGAACAGAGCATCT | 51667 |
rs79729826 | snp | A/G | 0.16846 | 0.236329 | intron-variant | NUB1 | GRCh38.p7 | 7:151342349 | CATTTTCCTAAGAAA[A/G]AATGAATGTGTCTTG | 51667 |
rs79969091 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339727 | TCGAATCTTTGTTTT[C/G]CAAGTCTATCAAAAA | 51667 |
rs80034940 | snp | A/C | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151351916 | TTGGCCCATCTGTAA[A/C]ACACACACACACACA | 51667 |
rs80067940 | snp | A/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151344488 | GCTAATTGTTCATAT[A/T]TTTTTTTTTTTTTAG | 51667 |
rs80071402 | snp | C/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151365320 | TTTTCTTCTCTCTCT[C/T]TTTTTTTTTTTTGGC | 51667 |
rs80189987 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | NUB1 | GRCh38.p7 | 7:151360557 | TAATGGTTTTGGGGT[A/T]GTATTGATGATTATT | 51667 |
rs80246097 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | NUB1 | GRCh38.p7 | 7:151375279 | TGTGTTGGAGAAATA[C/T]TAAGAGGTGGGAAAT | 51667 |
rs80280707 | snp | G/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151357202 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCG | 51667 |
rs111257297 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344065 | GGGCGCCTGTAGTCC[C/G]AGCTACTGGGGAGGC | 51667 |
rs111328332 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | NUB1 | GRCh38.p7 | 7:151344151 | GTACCACTGCACTCT[A/G]GCCTGGGCGACAGAG | 51667 |
rs111406010 | in-del | -/CA | 0 | 0 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341063 | TTTTACATACACACA[-/CA]TATATATATACTATA | 51667 |
rs111450429 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | NUB1 | GRCh38.p7 | 7:151357006 | ACAGGCGTGAGCCAC[C/T]GAACTCTGCCGTGTT | 51667 |
rs111618573 | snp | C/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151344913 | GCTGATGCAGGGGAA[C/T]TGCTTGAACCCAGGG | 51667 |
rs111661341 | in-del | -/T | 0.45946 | 0.136478 | intron-variant | NUB1 | GRCh38.p7 | 7:151357609 | AATTAAAGATTAAAG[-/T]TTTTTTTTTTTTTTT | 51667 |
rs111877317 | snp | A/G | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151346706 | GAGGCTTCTATGCTC[A/G]GGACCCTTCCAGACC | 51667 |
rs111923214 | snp | A/G | 0.5 | 0 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378718 | GAGCTGAGGTGACGC[A/G]GAGTCTCAGCCTCAT | 51667 |
rs112079550 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NUB1 | GRCh38.p7 | 7:151358164 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 51667 |
rs112088951 | snp | G/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151350532 | TCACTTCTCACTGTG[G/T]CCCTTCAGCTCCTAT | 51667 |
rs112275468 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349925 | GAAACCGGTAGTGGC[A/C]CCGAATGCCTGGCTG | 51667 |
rs112279534 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339713 | AGCAGATCTCAGACT[C/T]GAATCTTTGTTTTGC | 51667 |
rs112313256 | snp | C/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151350521 | TTGTCTTCTGGTCAC[C/T]TCTCACTGTGTCCCT | 51667 |
rs112322555 | snp | C/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151363006 | AGCTTAAAAGCTACT[C/T]CTGAACAGTACCCTT | 51667 |
rs112373605 | snp | C/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151345058 | CTCTTATTTTCTCTT[C/T]TCTCTTAGATAAGAG | 51667 |
rs112489136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151374625 | AAATTTTAAATGTAA[A/G]TATCTAGTTTTATTT | 51667 |
rs112678977 | snp | A/C | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151346810 | TTCTGGAGTTCTGTG[A/C]GTTGTTCTAGCAAAT | 51667 |
rs112679882 | snp | A/T | 0.0154538 | 0.0865337 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340823 | GTTTTTATTGATTCA[A/T]GAATCAGGATGGCAT | 51667 |
rs112699691 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358180 | GGGTTTCACCATGTT[G/T]GCCAGATGGTCTCAA | 51667 |
rs112723445 | snp | A/C | 0.0607341 | 0.163335 | intron-variant | NUB1 | GRCh38.p7 | 7:151352630 | AAAAATTTTTTGTAG[A/C]GATAGGATCTCTCTG | 51667 |
rs112728953 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151344560 | CTCCTGACCTCAGCT[C/T]CTGAACTCAGCCTCC | 51667 |
rs112821153 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUB1 | GRCh38.p7 | 7:151374796 | GTAGGGCAGGTGCTG[C/T]GCTGCGTCTCAGCAG | 51667 |
rs112923728 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151347443 | GTATATATAGGTTTA[C/T]GTTACTTACAAAATT | 51667 |
rs113015857 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362804 | ATGTGTGTGAGGAAA[C/T]TGCCCAGGGCTGGGC | 51667 |
rs113072841 | snp | A/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151350547 | TCCCTTCAGCTCCTA[A/T]CTCTGTGTGGCCTGG | 51667 |
rs113123759 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151354154 | GGTTCCTTTATTTTT[C/T]TTCCTATATAATTCA | 51667 |
rs113162143 | snp | C/T | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151369099 | TGCAAGCTCCGCCTC[C/T]CGGGTTCAAGCAATT | 51667 |
rs113342970 | snp | A/G | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151358677 | CAGTCCCTAGTGCCA[A/G]AAGGTTGGGACTACT | 51667 |
rs113373222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151374557 | AACAGGCAGTTTCCA[C/T]GGCAGAAAAAAGAGA | 51667 |
rs113425180 | snp | C/G | 0.5 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151361463 | TCTTGGGCATTTAAT[C/G]CCCAGACCAGGAATC | 51667 |
rs113490239 | snp | A/G | 0.166506 | 0.235645 | intron-variant | NUB1 | GRCh38.p7 | 7:151344070 | CCTGTAGTCCCAGCT[A/G]CTGGGGAGGCTGAGG | 51667 |
rs113576934 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | NUB1 | GRCh38.p7 | 7:151343165 | AAAAGCTAACGCTCT[A/G]AGTACTAATATGCTT | 51667 |
rs113646572 | snp | A/G | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151346294 | TGAATTTATTGTTAC[A/G]GTCTCTTGGTTTAGA | 51667 |
rs113699534 | in-del | -/A | 0.245916 | 0.249967 | intron-variant | NUB1 | GRCh38.p7 | 7:151364433 | CTCAAAAACAAAAAC[-/A]AAAAAAAACAAAAAA | 51667 |
rs113711755 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NUB1 | GRCh38.p7 | 7:151348710 | CCCCCCAAGTAGCTG[A/G]GCCTACAGGCACACG | 51667 |
rs113758600 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | NUB1 | GRCh38.p7 | 7:151374852 | TCTCGGCCCCGCAGG[A/T]CAGTGAGAGACAAAC | 51667 |
rs113798659 | snp | A/G | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151370230 | TAGCTGGAATTACAG[A/G]TGCCCACCACCACGC | 51667 |
rs113863983 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377885 | TGAGTGTCAGGCTTT[A/C]TATATATTCAGCATT | 51667 |
rs113879498 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | NUB1 | GRCh38.p7 | 7:151350060 | GCCTTTCCCTTGTAG[C/G]TAGACGAGGCGGAGA | 51667 |
rs113920358 | snp | C/T | 0.22437 | 0.248683 | missense, upstream-variant-2KB, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341801 | AACGGCGGCCGCTGC[C/T]GCATCCGGGCACTCT | 51667 |
rs114000471 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NUB1 | GRCh38.p7 | 7:151375475 | AACCCTACTACCTGC[A/C]TGACATTTTAAGTCT | 51667 |
rs114001960 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | NUB1 | GRCh38.p7 | 7:151360386 | AGTTATGGTGTAAAC[G/T]GGTGAATTTCTTCTT | 51667 |
rs114130767 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NUB1 | GRCh38.p7 | 7:151357502 | TTCAGTAGCTTCTTA[C/T]AATGAATGACTATGG | 51667 |
rs114195186 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | NUB1 | GRCh38.p7 | 7:151363182 | CAACAGATCCAGAAG[C/T]GACACAGAAGATAGA | 51667 |
rs114247250 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | NUB1 | GRCh38.p7 | 7:151376312 | CACATTTGTGCCCCT[A/G]CACGCGTTAGCACGC | 51667 |
rs114377053 | snp | C/T | 0.135484 | 0.22223 | intron-variant | NUB1 | GRCh38.p7 | 7:151347571 | CAAGTGATTCTCCCA[C/T]CTCAGCCTTGGGAGT | 51667 |
rs114412640 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NUB1 | GRCh38.p7 | 7:151376941 | CGGGCCGGCCACCTG[G/T]ACAGTGTGGCCAGCA | 51667 |
rs114541181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151356347 | CCATCTCCAGCCTCG[C/T]AAACAGAAAATGTCA | 51667 |
rs114543418 | snp | C/T | 0.0260105 | 0.111035 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378071 | TTTGTGGGTTTTCTT[C/T]GTTGTTGTTGTTGTT | 51667 |
rs114624838 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | NUB1 | GRCh38.p7 | 7:151347671 | CACTTTGTTGCCCAG[A/G]TTGGTCTTGAAGTCC | 51667 |
rs114741499 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | NUB1 | GRCh38.p7 | 7:151349643 | TCTCAAGCAGGGCCG[A/G]GGAGATCTGGGTGGG | 51667 |
rs114748994 | snp | A/G | 0.00110899 | 0.0235216 | missense | NUB1 | GRCh38.p7 | 7:151375909 | CTGAAACCGACAACC[A/G]TCAAGAAAGTCCTTC | 51667 |
rs114894405 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NUB1 | GRCh38.p7 | 7:151345227 | TAAACCATAGTAATT[C/T]ATATTTAATGACAGA | 51667 |
rs115026422 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | NUB1 | GRCh38.p7 | 7:151363417 | TTAAATGTTACATAA[A/G]GCAATAGAAACTATC | 51667 |
rs115173356 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NUB1 | GRCh38.p7 | 7:151342720 | ACATTAAATCTTATT[C/T]GGTGTAACCCTGGAG | 51667 |
rs115234623 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | NUB1 | GRCh38.p7 | 7:151350941 | ATGAAGTGCTGATGC[A/G]TCCACAACGTGGGTG | 51667 |
rs115237718 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | NUB1 | GRCh38.p7 | 7:151370028 | CTTGCCTAGTCCAAT[C/T]GTGGTCCTTTGGGTC | 51667 |
rs115347539 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NUB1 | GRCh38.p7 | 7:151373865 | CTCCTTCCTGCCCCA[C/T]GGGCATCTCACTTCC | 51667 |
rs115424154 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | NUB1 | GRCh38.p7 | 7:151360975 | TTATACAGATGGGGT[C/T]TCCCTGTGTTGCTCA | 51667 |
rs115425022 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340224 | CCCTCAGAAAAAAAT[G/T]TCAGAACAGTTTCTG | 51667 |
rs115458421 | snp | C/T | 0.00100105 | 0.02235 | intron-variant | NUB1 | GRCh38.p7 | 7:151349249 | AAAAAAAGTGAGTAA[C/T]TTCCCTAAATTTGAG | 51667 |
rs115466605 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | NUB1 | GRCh38.p7 | 7:151361838 | TCTGCCTCTTTCTGG[A/G]TGTCAGTTTCATTCT | 51667 |
rs115698276 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NUB1 | GRCh38.p7 | 7:151352321 | AGGACCTTGTCTCCT[A/G]CAGTTTCAAATAGCC | 51667 |
rs115799346 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | NUB1 | GRCh38.p7 | 7:151346661 | AACACATCCACATGT[C/T]GGGATGTACACCCCC | 51667 |
rs115819672 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | NUB1 | GRCh38.p7 | 7:151364465 | AAAACAAAAAAACTG[G/T]AAGACAAACATAATA | 51667 |
rs115836880 | snp | A/G | 0.00279013 | 0.0372462 | intron-variant | NUB1 | GRCh38.p7 | 7:151360096 | AATATAATTTGCCTT[A/G]TTATATTTTAAAGTG | 51667 |
rs115946617 | snp | C/T | 0.039522 | 0.134904 | intron-variant | NUB1 | GRCh38.p7 | 7:151343021 | TTCAAATTGCTTGGC[C/T]CCAGTAACCAGCCTG | 51667 |
rs116161212 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NUB1 | GRCh38.p7 | 7:151356002 | CTTGGGGGCAGCACT[A/G]GATCACACAGTTGGG | 51667 |
rs116449107 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | NUB1 | GRCh38.p7 | 7:151363634 | CCCCCAGATGCAATG[A/T]CTTTAATGACCCCAA | 51667 |
rs116502766 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NUB1 | GRCh38.p7 | 7:151351873 | TTGCTATGACCTTCA[A/G]CACGGTGTTTTATCT | 51667 |
rs116585761 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | NUB1 | GRCh38.p7 | 7:151352512 | ACAGTGGCATAAATA[C/T]AGCTCATTGCAACCT | 51667 |
rs116669540 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NUB1 | GRCh38.p7 | 7:151361070 | ACAGGTGTGAGCCAC[C/T]GCACCCAGCCTCCCT | 51667 |
rs116685299 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | NUB1 | GRCh38.p7 | 7:151347326 | AGGATCACTTGAACC[C/T]GGGAGTTGGAGACTG | 51667 |
rs116748729 | snp | A/G | 0.030665 | 0.119967 | intron-variant | NUB1 | GRCh38.p7 | 7:151376148 | AAGCAGGAAAACTGG[A/G]GAAGTGTCAGGAAGT | 51667 |
rs116860296 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NUB1 | GRCh38.p7 | 7:151353017 | TGATTTAGAAGTTTA[C/T]TAAAATAAAAATGTA | 51667 |
rs116911095 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | NUB1 | GRCh38.p7 | 7:151359105 | TGTTTTGGAAATACT[A/G]AAGTTGACAAACAAC | 51667 |
rs116976414 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | NUB1 | GRCh38.p7 | 7:151347807 | TTTTATCATGAACAT[C/G]TCTTCTGTCATAAAT | 51667 |
rs117412509 | snp | A/T | 0.0445623 | 0.142462 | intron-variant | NUB1 | GRCh38.p7 | 7:151355760 | ATAGGCAGTTCTGAT[A/T]TTTATAGGGAAAACC | 51667 |
rs117705450 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NUB1 | GRCh38.p7 | 7:151343246 | GGGCCACCCAGGTTG[C/T]ACACAGCAGCCTCAT | 51667 |
rs117817183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151349980 | CAGAAGGGGCAGGGT[A/G]AGGACTGTGAGTCAT | 51667 |
rs117924342 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151373144 | GCAGGATCAGGTCTC[C/T]GGAAGGAAGGAGTCT | 51667 |
rs117938037 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | NUB1 | GRCh38.p7 | 7:151359670 | TAGTCCTAGCTGCTC[A/G]GCAGGCTGAGGCAGG | 51667 |
rs118017776 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUB1 | GRCh38.p7 | 7:151374548 | GTTTAGTGAAACAGG[C/T]AGTTTCCACGGCAGA | 51667 |
rs137946032 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371701 | CCCTCGGAGTTCCAA[C/T]GTTCTAGGTATGAGC | 51667 |
rs137968562 | in-del | -/T | 0.271162 | 0.249103 | intron-variant | NUB1 | GRCh38.p7 | 7:151360628 | GTACTTATTTTTTTT[-/T]GAGACAGAGTCTCAC | 51667 |
rs138050080 | in-del | -/A | 0.0298908 | 0.118541 | intron-variant | NUB1 | GRCh38.p7 | 7:151368993 | TTACTCCAGATTGGG[-/A]AGGAAGGAGAAACTT | 51667 |
rs138056475 | snp | C/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151365902 | GTCCTTTTTTTTTTA[C/T]TCCATGCATATTTTG | 51667 |
rs138180788 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378104 | AGCCATGTGACAGAG[A/G]CTCTTTCTAAAAGTA | 51667 |
rs138200453 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151365258 | ATGTACCCCTCTAAT[A/G]TGAGACCTCTGCTTT | 51667 |
rs138292453 | snp | A/T | 0.497933 | 0.032082 | intron-variant | NUB1 | GRCh38.p7 | 7:151361016 | GAACTCCTGGACTCA[A/T]GTGATCCTCCTGCCT | 51667 |
rs138300503 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151356861 | TAGCTGGGATTACAG[A/G]CATGTGCCACCACGG | 51667 |
rs138370645 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378622 | TGCTGTGAAAGATGC[C/T]GCACGCCAAGCGGGG | 51667 |
rs138570836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343471 | AATAGAAGAAAGAAA[C/T]TTATCTTGGTAATAT | 51667 |
rs138601075 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUB1 | GRCh38.p7 | 7:151345591 | ATTAGTGGTGAGCGG[A/G]TACCCACTTTTTACT | 51667 |
rs138632381 | in-del | -/AGTT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363757 | ACCTTTCTTGAAAAA[-/AGTT]AGGTAAGTTTGGCTT | 51667 |
rs138749362 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151360616 | AATGGTGATATTATT[A/C]CTTCTGTACTTATTT | 51667 |
rs138810935 | snp | C/G | 0.0197834 | 0.0975812 | intron-variant | NUB1 | GRCh38.p7 | 7:151371180 | AGTTACGATGCCTTT[C/G]GCTGAAAGCAACAAC | 51667 |
rs138898982 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NUB1 | GRCh38.p7 | 7:151366346 | TGCCTTGTCAGAGCC[A/G]TCATCAGCTGAGGCA | 51667 |
rs139182268 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151358791 | GTTTTGGGGCCGGGC[A/G]CGGTGGCTCACGCCT | 51667 |
rs139320700 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NUB1 | GRCh38.p7 | 7:151347011 | GTGTCAGAATTGAAT[C/T]GTAGGACTTCCAGTT | 51667 |
rs139429566 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | NUB1 | GRCh38.p7 | 7:151366708 | GCAAGTGGTGGTAAG[A/C]TTTGATTCCTAAGCC | 51667 |
rs139522176 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151363954 | GCCCACTACCACTCC[C/T]GACTAGTTTTTGTAT | 51667 |
rs139694544 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NUB1 | GRCh38.p7 | 7:151374962 | AGATGCTGGGGCAGC[A/G]CGGCGGGCAGGAAGC | 51667 |
rs139745397 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | NUB1 | GRCh38.p7 | 7:151352942 | AGAAATAATGACTTC[A/C]CTTTTTTTCTCAATG | 51667 |
rs139887812 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NUB1 | GRCh38.p7 | 7:151367188 | ATTTGTGTTTATTCC[A/T]GTTAAAGTATTTGAA | 51667 |
rs139905681 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151353433 | CTTATAACTTGGTGA[C/T]GGGGGAGGTTGTGCT | 51667 |
rs140025640 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151375588 | TTTTCTTGGATGCTG[C/T]TTCCACCTGCTCTCC | 51667 |
rs140086316 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151350024 | TAAGGTCACAGGAGT[C/T]ATGTGTCCACCGGAC | 51667 |
rs140305826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346071 | AATTTCCTAGCATGT[A/G]CTTCTCTGCTCTCAT | 51667 |
rs140795186 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | NUB1 | GRCh38.p7 | 7:151355633 | AGCCATGATCGTGTC[A/C]CTGCACTCCAGCCTG | 51667 |
rs140841499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151370892 | ATCATTTGGAAAACA[A/G]TTCTCATCACTGTAT | 51667 |
rs140946872 | in-del | -/CC | 0.0228947 | 0.104514 | intron-variant | NUB1 | GRCh38.p7 | 7:151373912 | GCAGCACTTCCACCA[-/CC]CCTCTGCCTCTGTGG | 51667 |
rs141076898 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151349663 | ATCTGGGTGGGGTCA[C/T]CTCCTCTCATTGCCA | 51667 |
rs141102034 | in-del | -/G | | | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378934 | CCGGCTGTGGAGGCA[-/G]GTTCTGGGCATGCGC | 51667 |
rs141115307 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NUB1 | GRCh38.p7 | 7:151360492 | TCTGTACATGTGCTA[C/T]GTTGCTAGTCGGAAC | 51667 |
rs141208416 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | NUB1 | GRCh38.p7 | 7:151370165 | GTGGCGTGATCACTG[C/G]AACCTCTGCCTCCCA | 51667 |
rs141312982 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NUB1 | GRCh38.p7 | 7:151365434 | GCCCACGCTCTTGAT[A/G]CTTAGTAAAACATGA | 51667 |
rs141319984 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377686 | CAGGGTGCCACATGG[C/G]TTCCTGTGCCACCCT | 51667 |
rs141639497 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378170 | TCCTCACTGCGCCAC[A/G]CACTCCTCTGTAGAT | 51667 |
rs141697504 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357901 | AGGCATGAGCCACTG[C/T]GCCCGGCCGGATTAA | 51667 |
rs141724967 | in-del | -/CAA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371189 | GCCTTTGGCTGAAAG[-/CAA]CAACAACAACAAAAA | 51667 |
rs141740498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151356382 | GTGGTGAGCACTGGC[A/C]TCCAATGGGCCTCAC | 51667 |
rs141765389 | snp | A/T | 0.471292 | 0.116318 | intron-variant | NUB1 | GRCh38.p7 | 7:151361024 | GGACTCATGTGATCC[A/T]CCTGCCTTGGCCTCC | 51667 |
rs141813162 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | NUB1 | GRCh38.p7 | 7:151361033 | TGATCCTCCTGCCTT[A/G]GCCTCCCAAAGTGCT | 51667 |
rs141818509 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151352653 | TCTCTCTGTTGCCCA[G/T]GCTGGTCTTGAATTC | 51667 |
rs141918494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151360704 | GCTCACTGCAACTTC[C/T]ATCTCCTGGGCTCAA | 51667 |
rs141924405 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151346726 | CCTTCCAGACCTTGC[C/G]TTAGTACCTCTTCAT | 51667 |
rs142066587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357370 | CTCAGATGATCCGCC[C/T]GCCTCGGCCTCCCGA | 51667 |
rs142107276 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NUB1 | GRCh38.p7 | 7:151372900 | GGCGCTGTGGGCACT[C/T]CAGGGCCACACCAGG | 51667 |
rs142190355 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339905 | ATTCTCAGCCTCATG[C/T]TTGTATCCAGAACTG | 51667 |
rs142463888 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | NUB1 | GRCh38.p7 | 7:151364556 | TTGAGACGGAGTCTC[C/G]CTCTGTCGCCCACGC | 51667 |
rs142496469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354501 | TTAAAATCTGTTTGC[A/T]TCTATGTTTACCCTT | 51667 |
rs142586708 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151366716 | TGGTAAGCTTTGATT[A/C]CTAAGCCCTGATTTC | 51667 |
rs142590700 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151348977 | GGGCGACCTCCACTC[A/G]TCAGAGTTGATGGCC | 51667 |
rs142866039 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151344909 | GGAGGCTGATGCAGG[A/G]GAATTGCTTGAACCC | 51667 |
rs143344537 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151350765 | CCTGGGTGGCTTGCC[A/G]CCCACATATATATTA | 51667 |
rs143463987 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NUB1 | GRCh38.p7 | 7:151349779 | GAAATAAGAGCATAG[A/G]CTCCAGCCCTACTGG | 51667 |
rs143528729 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NUB1 | GRCh38.p7 | 7:151353535 | GACTTGTCCAGTCCC[A/G]GATGTCAGTAGCGCA | 51667 |
rs143601519 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341012 | GTCCCAAGACCCACA[A/G]TGGATGCCTGAAACC | 51667 |
rs143697076 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | NUB1 | GRCh38.p7 | 7:151376568 | CGGCTGTCCACTCGT[A/G]TGGCTGACGGGGGTG | 51667 |
rs144146617 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NUB1 | GRCh38.p7 | 7:151366245 | AAATTTTGCCTGCAC[A/T]CAGGCCCTCAGAAAT | 51667 |
rs144151349 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151361688 | AAATATTTATAGTTT[C/T]CCATTGGTCAGTGCC | 51667 |
rs144484765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151368440 | GGTGAGAAATGCCAC[A/G]TGCACAGCTGAAATT | 51667 |
rs144551435 | snp | A/G | 0.030665 | 0.119967 | intron-variant | NUB1 | GRCh38.p7 | 7:151375022 | ACGTGCTGGGGGCGG[A/G]GCTGGGGGGACAGAG | 51667 |
rs144567260 | snp | C/T | 0.497803 | 0.033074 | intron-variant | NUB1 | GRCh38.p7 | 7:151361027 | CTCATGTGATCCTCC[C/T]GCCTTGGCCTCCCAA | 51667 |
rs144691015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343301 | TTTCTCCTCCCTGTC[C/G]TGATTAGCCTAATTC | 51667 |
rs145366092 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | NUB1 | GRCh38.p7 | 7:151364084 | CAGGTGTGAGCCACC[A/G]CGCCTGGCCTAAAAT | 51667 |
rs145634073 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340650 | GCATCCTCAGGTTAC[A/G]TGCGAAACCTTCCAT | 51667 |
rs145768979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376080 | CCAGGTGTAACCTGC[C/T]CACCTCAGAGGCCAC | 51667 |
rs145849650 | snp | C/T | 0.00216105 | 0.0328002 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151355889 | GGAGCAAAATGAGGC[C/T]AAACTCAAAGAAAAA | 51667 |
rs145874890 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367731 | TTGCCGTCAGTCATA[A/G]TGAAGCCATGGACAT | 51667 |
rs146009588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151353229 | GGGAGGCCATGGTGG[C/T]GTGCGTTCCAGACTG | 51667 |
rs146282285 | in-del | -/AC | 0.0629771 | 0.165899 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341056 | CACCCCATTTTACAT[-/AC]ACACACATATATATA | 51667 |
rs146503718 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | NUB1 | GRCh38.p7 | 7:151344979 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 51667 |
rs146523163 | snp | G/T | 0.00169517 | 0.0290639 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349109 | GACAGACTAGAATGC[G/T]GTGAAAATGAAGTAG | 51667 |
rs146561231 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NUB1 | GRCh38.p7 | 7:151369071 | GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 51667 |
rs146624264 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | NUB1 | GRCh38.p7 | 7:151375198 | TTTGTAACTATGTAC[A/T]TGTATATTTAACATA | 51667 |
rs146680573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349997 | GGACTGTGAGTCATC[C/T]CCAATGATTGATAAG | 51667 |
rs147080634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151360277 | ACTTGGTGAACACCA[A/G]CTTTAAGGAAGATGG | 51667 |
rs147360785 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151366423 | TCAGCCCTGGCTGTA[C/T]ACTAGAATCAGCTGG | 51667 |
rs147429602 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NUB1 | GRCh38.p7 | 7:151371647 | CCCACAGAAAGTGAG[C/T]TCCTATCGGAGCTTT | 51667 |
rs147466394 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NUB1 | GRCh38.p7 | 7:151347503 | TGATCTGTTGCCCAG[G/T]CTGGAGTGCAATGGC | 51667 |
rs147535452 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUB1 | GRCh38.p7 | 7:151350900 | GGTCTATTCATACGA[C/T]GGAAAACTGTTCACA | 51667 |
rs147786952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151359726 | AGGTTGCAGTGACCC[A/G]AGATCGCACCACTGC | 51667 |
rs147803470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151362040 | CTGCAGTTATAAAGA[C/T]ATGGTTGATCTTCAT | 51667 |
rs147835858 | snp | A/C/T | 0.00119752 | 0.0244452 | intron-variant | NUB1 | GRCh38.p7 | 7:151376953 | CTGGACAGTGTGGCC[A/C/T]GCAAGAGGCACAGTC | 51667 |
rs147903940 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NUB1 | GRCh38.p7 | 7:151344869 | GCCGGGCGTGGTGGC[A/G]CATGCCTGTAATCCC | 51667 |
rs148151648 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151346430 | TTGTGCTCATGAGGC[C/T]TGGTTGCCCCTAGAT | 51667 |
rs148294264 | snp | C/T | 0.031825 | 0.122064 | intron-variant | NUB1 | GRCh38.p7 | 7:151357270 | CTGGGATTATAGGCA[C/T]GCACCACCATGCCTG | 51667 |
rs148312629 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151370787 | CTGTGAGTGAGAATA[C/T]GCGGTGTTTGGTTTT | 51667 |
rs148457622 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NUB1 | GRCh38.p7 | 7:151348818 | CACCTCAAGTGATGC[A/G]CCTGCCTCGGCCTCC | 51667 |
rs148610977 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | NUB1 | GRCh38.p7 | 7:151359527 | CTCACGCCTGTAATC[C/T]CAGCATTTTGGGAGG | 51667 |
rs148825297 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NUB1 | GRCh38.p7 | 7:151354437 | CCAGCTAGTTTTCCA[A/G]AAATGTGTTCACATT | 51667 |
rs148963851 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151376190 | TTGCTGCCTTTGTCT[A/G]TGCACCACTGTTTGC | 51667 |
rs149041581 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | NUB1 | GRCh38.p7 | 7:151368517 | ACACCCAGCCTCTTA[-/C]CCTCGTGTTGTGCTG | 51667 |
rs149445928 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NUB1 | GRCh38.p7 | 7:151372170 | CTAAGAGGCCATCCC[A/G]GCTTGTTGTGACCAT | 51667 |
rs149567868 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151356978 | CACCTTGGCCTCCCA[A/G]ACTGCTGGGATTACA | 51667 |
rs149647109 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | NUB1 | GRCh38.p7 | 7:151344860 | TGAAAATTAGCCGGG[C/T]GTGGTGGCGCATGCC | 51667 |
rs149764438 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | NUB1 | GRCh38.p7 | 7:151376035 | CAGCAGGACTGGGGG[A/T]GTCCGTGCTGAAACC | 51667 |
rs149804762 | in-del | -/ACCACC | 0.02016 | 0.0983543 | intron-variant | NUB1 | GRCh38.p7 | 7:151349895 | GCCCGGAGGACCACT[-/ACCACC]ACCACCTAGACGCGG | 51667 |
rs149818337 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151367474 | AGCAGTAATGGTTTA[C/T]GTGAATGAGTCACAG | 51667 |
rs149934586 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NUB1 | GRCh38.p7 | 7:151353012 | AAAAGTGATTTAGAA[A/G]TTTACTAAAATAAAA | 51667 |
rs149953605 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUB1 | GRCh38.p7 | 7:151359136 | TTCTGAAAAAACTAG[A/G]TGATTAAGAATAGAA | 51667 |
rs150021881 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NUB1 | GRCh38.p7 | 7:151348075 | GAAAATTCAAAATTC[A/G]AAATACTTCAGTGTG | 51667 |
rs150097470 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378523 | GTCTGGGTGACTAGC[A/T]CTTCATTTTGATTGC | 51667 |
rs150127971 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340043 | TTCACTGCCTTCAAA[C/T]AGATGTTTTCTGACT | 51667 |
rs150131115 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NUB1 | GRCh38.p7 | 7:151371146 | ATCCTTCTCCCTCTT[C/T]CACCCAACAGATGTT | 51667 |
rs150218549 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NUB1 | GRCh38.p7 | 7:151365766 | AGAAATGTTGAGAGA[A/G]ATGAAAATAAATATA | 51667 |
rs150264787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151360502 | TGCTATGTTGCTAGT[C/T]GGAACTTTCCATTAT | 51667 |
rs150532999 | snp | C/T | 0.000116814 | 0.00764154 | missense | NUB1 | GRCh38.p7 | 7:151367015 | GTGTGGTGTTACTTC[C/T]GCCTGGAACAGCTGG | 51667 |
rs150641405 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NUB1 | GRCh38.p7 | 7:151352720 | GGTGTTGGGATTACA[A/G]GCGTGAGCCACCGGG | 51667 |
rs150694159 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NUB1 | GRCh38.p7 | 7:151346770 | TGTATCCTTTGTAAT[G/T]AACTATATTCATAAG | 51667 |
rs150867880 | snp | C/T | 0.154661 | 0.231107 | intron-variant | NUB1 | GRCh38.p7 | 7:151344333 | ATTATTATTTTGAGA[C/T]GGAGTCTCACTCTGT | 51667 |
rs150962072 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NUB1 | GRCh38.p7 | 7:151355281 | TTAGTTGATTCTATT[A/G]TCGCTAGCTGATTTT | 51667 |
rs151120280 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151360468 | AGCAGGTAGGATATC[C/T]TCTCTTCTTCTGTAC | 51667 |
rs151208071 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | NUB1 | GRCh38.p7 | 7:151344916 | GATGCAGGGGAATTG[C/G]TTGAACCCAGGGGGC | 51667 |
rs151238324 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363468 | AAAAAAAAAAAAAAA[-/A]TGAACAGAGCATCTG | 51667 |
rs151314599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151364872 | TAAATAAATATTTTA[C/T]GTTTATTTTAATATC | 51667 |
rs180785057 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NUB1 | GRCh38.p7 | 7:151359384 | GGAGGTGGAGCTTGC[A/G]GTGAGTCGAGATCGC | 51667 |
rs180789808 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377493 | CTTGGTGTTTTACCC[C/T]GAAACAGGAAGGAAC | 51667 |
rs180805607 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151342757 | TTTGCTCCCTGGAGT[A/G]TCTGACACGCACTGG | 51667 |
rs180810841 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151350692 | GTAACTATTCTTATT[C/T]TATATATTTTCTTTA | 51667 |
rs180841625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151367279 | ATATTTATAAAGTGT[C/T]CAATGTTTTACAAAT | 51667 |
rs180908121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151373800 | GAGTGCTGGGTTGGC[A/G]AGCAGCCCATCCTGA | 51667 |
rs180926563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151355565 | GTAGTCCCAGCTCCT[C/T]GGGAGGCTGAGGTGC | 51667 |
rs180944737 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | NUB1 | GRCh38.p7 | 7:151364397 | CTGCACTCCAGCCTG[C/G]AGGAGAGAGCGAGAC | 51667 |
rs180949142 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151345222 | TCATTTAAACCATAG[C/T]AATTTATATTTAATG | 51667 |
rs181125358 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378255 | CGAGTGGATTGAGTG[C/T]CAGGTGCATCCAAGA | 51667 |
rs181331224 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356916 | GAGACAGGGTTTCTC[C/T]ATGTTGGTCAGGCTA | 51667 |
rs181411604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343174 | CGCTCTAAGTACTAA[C/T]ATGCTTTGCTGTGAT | 51667 |
rs181427852 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151350035 | GAGTCATGTGTCCAC[C/T]GGACAGGGGGCCTTT | 51667 |
rs181611355 | snp | A/G | 0.000187746 | 0.00968698 | intron-variant | NUB1 | GRCh38.p7 | 7:151366912 | AAATGCTGCTTGGCA[A/G]TGATGTCACTGTCCT | 51667 |
rs181613119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151350391 | CTTCCCAGGCACTGG[C/T]GCTACCGCTAGACCA | 51667 |
rs181658340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151364564 | GAGTCTCGCTCTGTC[A/G]CCCACGCTGGAGTGC | 51667 |
rs181708834 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346710 | CTTCTATGCTCAGGA[A/C]CCTTCCAGACCTTGC | 51667 |
rs181741630 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347354 | CTGTAGTATGCTATG[A/G]TCCCACCTGTGAATA | 51667 |
rs181754952 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364917 | GTAACAGTGTTGAAT[A/G]TTAATGCTACTAAAA | 51667 |
rs181790122 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378578 | TGTGAGGAGATGATG[A/G]AAGGATGATCTCAGA | 51667 |
rs182048528 | snp | G/T | 0.368119 | 0.220336 | intron-variant | NUB1 | GRCh38.p7 | 7:151360991 | TCCCTGTGTTGCTCA[G/T]GCTGATCTTGAACTC | 51667 |
rs182188203 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151344300 | AAAAATTCTGACATA[A/G]AAAATATTTATATAT | 51667 |
rs182203228 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151361011 | ATCTTGAACTCCTGG[A/G]CTCATGTGATCCTCC | 51667 |
rs182226211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372787 | TGCTGCCCTGTGCAG[C/T]GGGGCTGGAGCTGGG | 51667 |
rs182302880 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151354717 | GGGCCACAGAGTTAA[A/C]ACGGTAGATGGAGCC | 51667 |
rs182305826 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341478 | AGCCAGGATCCATTT[C/T]CTCTTGATGGCTGGC | 51667 |
rs182317005 | snp | C/T | 0.000380829 | 0.0137938 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151375901 | TTCCAATCCTGAAAC[C/T]GACAACCGTCAAGAA | 51667 |
rs182320801 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151357128 | CTTGAGCGATCCTCC[C/T]GCCTCCGCCTTCTGG | 51667 |
rs182546942 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151370812 | GGTTTTTTGTTCTTG[C/G]GATAGTTTACTGAGA | 51667 |
rs182642122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151347831 | CATAAATTTATGCTT[A/G]CACCATAATTTTTAC | 51667 |
rs182783053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151352600 | GGCATGGGCTACCAG[A/G]CCTGGCTAATTTTTA | 51667 |
rs182790488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151362448 | TCTCCAAGTAAGCTA[C/G]AAGTTTTGTCACAAC | 51667 |
rs182809433 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151351853 | TTCCCTAATGTATTA[A/C]TAGCTTGCTATGACC | 51667 |
rs182957959 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340347 | AAAAGAAAGGCTTTA[C/T]TGTGAGTTGACTGTC | 51667 |
rs182982561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365106 | TGAGATTACAGGTGT[A/G]AGCCACCACACCCAG | 51667 |
rs183020717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151356412 | CCCTGTGCTTTTCAG[C/T]GCATTAGTACAAAAT | 51667 |
rs183064180 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NUB1 | GRCh38.p7 | 7:151367672 | CTGTGTGGCATGAGG[A/G]ATGTTATCATACCAC | 51667 |
rs183154632 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151352336 | ACAGTTTCAAATAGC[C/T]GTCTAGTAAGATGGC | 51667 |
rs183160944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369560 | GCACAGGTTAAAAAA[C/T]TATAATCATTTGAAA | 51667 |
rs183389243 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NUB1 | GRCh38.p7 | 7:151365551 | TCACTGGGACCAGAA[C/T]GTGCCTAGAGGCAGG | 51667 |
rs183642331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151356931 | CATGTTGGTCAGGCT[A/G]GTCTTGAACTCCCGA | 51667 |
rs183661346 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151348353 | ACTTGATTTGTTCTC[A/T]CAAGTTTGAAAAATT | 51667 |
rs183753569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151344995 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAGAAAA | 51667 |
rs183866718 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340914 | GGTAGAAAAGGGCTA[A/C]AGAAAGCAGCAACAG | 51667 |
rs183868646 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151375434 | AAGATTAAGTATTGT[A/G]TGATGAAGAAATCAA | 51667 |
rs183881595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151371853 | GGCTCCAATGATCCT[C/T]CTGCCAAGAGCTCTC | 51667 |
rs183886122 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151353633 | AAGACATCTGTGCTG[C/T]GGAGTGATACACAAT | 51667 |
rs183961522 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151359507 | CAAGCAGCCGGGCAC[C/T]GTGGCTCACGCCTGT | 51667 |
rs183968092 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378092 | TGTTGTTGTTCTAGC[C/T]ATGTGACAGAGGCTC | 51667 |
rs184016240 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | NUB1 | GRCh38.p7 | 7:151350291 | CTGACTAATGTCAGG[A/C]CTTCCACAAGAGGTG | 51667 |
rs184020517 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151376269 | TGGGAAACCCATCCA[C/G]CTTTGTATCCCAAGT | 51667 |
rs184300655 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NUB1 | GRCh38.p7 | 7:151358461 | CAAGTGAGCGTCACC[A/G]CCTGAGCTCCACCTC | 51667 |
rs184450733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349809 | GGTCTGTGGTTTTTC[C/T]CCTCATGTGCGGAGA | 51667 |
rs184496399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151372147 | CCAGGCCGTGAGACG[C/T]AGCCTTCCTAAGAGG | 51667 |
rs184600650 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NUB1 | GRCh38.p7 | 7:151366587 | TTTGCAGTCAGGATT[A/G]GAAGTCACAGCTTTA | 51667 |
rs184618752 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | NUB1 | GRCh38.p7 | 7:151364452 | AAAAACAAAAAAAAA[A/C]ACAAAAAAACTGTAA | 51667 |
rs184744852 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151345907 | GTTCATTTTTCCAAA[A/T]TAGGTTTTTTCTAAC | 51667 |
rs184787855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151365964 | GATTTTGTAGTTTTA[C/T]ACAAGAGCATTCTTA | 51667 |
rs184792171 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348965 | TGCAGTGTAACGGGG[C/T]GACCTCCACTCATCA | 51667 |
rs184810407 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | NUB1 | GRCh38.p7 | 7:151366783 | TTATAAACACAGCTC[C/G]CTTCCTAAACATTAG | 51667 |
rs184941767 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151364085 | AGGTGTGAGCCACCG[C/T]GCCTGGCCTAAAATT | 51667 |
rs185122397 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341618 | GCTTAGCTCCGCCCC[A/G]TCGCGGCTCCGCCCC | 51667 |
rs185392907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151363232 | AAAACAGTGACTGTA[A/G]TCCATCTGCTGAAGA | 51667 |
rs185418110 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NUB1 | GRCh38.p7 | 7:151359161 | ATAGAAAGTGAGGCC[A/G]GGCACGGTGGCTCAT | 51667 |
rs185541608 | snp | C/T | 5.12046e-05 | 0.00505961 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376708 | CAACGTCCAGCTGGC[C/T]GCCCAGACCCTTGCT | 51667 |
rs185586993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342474 | AAATTTTTAAAGGAT[C/T]GTTATAACGTTTCAC | 51667 |
rs185638292 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151356075 | TTTTAAGGCTGTCAT[C/T]ATCATAACTGTTTAA | 51667 |
rs185715358 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378319 | ACAGGATGGATCATG[C/T]GGAGCCGGCTGAAAT | 51667 |
rs185777726 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369018 | AAACTTGTCCTTTTT[C/T]TTTTCTTGAGACAGA | 51667 |
rs185781789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151351876 | CTATGACCTTCAGCA[C/T]GGTGTTTTATCTGAT | 51667 |
rs186036483 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151347201 | AATATGTTAAACATC[A/G]TTAACATAGGTATAT | 51667 |
rs186127896 | snp | C/T | 8.32938e-05 | 0.0064529 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151367018 | TGGTGTTACTTCCGC[C/T]TGGAACAGCTGGAAT | 51667 |
rs186133501 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151350562 | TCTCTGTGTGGCCTG[C/G]TTTTTCCTAGGTTAT | 51667 |
rs186140329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151351186 | TCCAGCTGTGTGAGA[C/T]GGCCCCTCTGAGCAG | 51667 |
rs186244297 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151367449 | TGTAAATGCAGAAAA[C/T]AGACATTTCAGCAGT | 51667 |
rs186255446 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348649 | GGCACAATCTTGGCT[C/T]ACTGCAGCCTCTGCC | 51667 |
rs186263116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151374977 | GCGGCGGGCAGGAAG[C/T]AGAGTGGTAGGAGCT | 51667 |
rs186271923 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NUB1 | GRCh38.p7 | 7:151365076 | TGATTTTCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 51667 |
rs186275852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151347395 | TCCAGCCTGGGCAAC[A/G]TAGTGAGACCCCGTC | 51667 |
rs186354437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343493 | TGGTAATATTAACTC[A/G]TATTTTTTCCACTCT | 51667 |
rs186555745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151359975 | TCAGTATTTAAATGA[A/G]ATAAAGCTTTAATTA | 51667 |
rs186789662 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | NUB1 | GRCh38.p7 | 7:151344386 | TGCCATCTCGGCTCA[C/G]TACAACCTCTGCCTC | 51667 |
rs186798823 | snp | A/T | 0.497749 | 0.0334707 | intron-variant | NUB1 | GRCh38.p7 | 7:151361031 | TGTGATCCTCCTGCC[A/T]TGGCCTCCCAAAGTG | 51667 |
rs186919313 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341482 | AGGATCCATTTCCTC[C/T]TGATGGCTGGCAAAC | 51667 |
rs186929358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151356803 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 51667 |
rs186935191 | snp | A/C/G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357371 | TCAGATGATCCGCCC[A/C/G/T]CCTCGGCCTCCCGAA | 51667 |
rs187004249 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151376060 | GAAACCTTGGCTCCC[A/T]GGCTCCAGGTGTAAC | 51667 |
rs187141098 | snp | C/T | 0.368119 | 0.220336 | intron-variant | NUB1 | GRCh38.p7 | 7:151361000 | TGCTCAGGCTGATCT[C/T]GAACTCCTGGACTCA | 51667 |
rs187162347 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340382 | AGACATGAGGAAACC[C/T]TCAGCTCTGTCTCCT | 51667 |
rs187169476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151364587 | TGGAGTGCAATGGCA[C/T]GATCTCGGCTCACTG | 51667 |
rs187182176 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NUB1 | GRCh38.p7 | 7:151373121 | CTGTTGCCTGGGCTG[A/G]GCAGGAGGCAGGATC | 51667 |
rs187292047 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344248 | GTTAATCAGAAAATA[C/T]GCAAAATTTTCCTAG | 51667 |
rs187331924 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378845 | CCAGCTGTTTTTAGC[C/T]ATCATAGAAGCAATG | 51667 |
rs187375458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365744 | GTTCTCAAACATTCA[C/T]GAAATTAGAAATGTT | 51667 |
rs187433041 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151355284 | GTTGATTCTATTGTC[A/G]CTAGCTGATTTTAAC | 51667 |
rs187455732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151353233 | GGCCATGGTGGCGTG[C/T]GTTCCAGACTGAGAG | 51667 |
rs187660115 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151348817 | TCACCTCAAGTGATG[C/T]GCCTGCCTCGGCCTC | 51667 |
rs187715616 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371118 | AAAAAAACCAGTGTA[G/T]ATAGTGCAGTTGATC | 51667 |
rs187806163 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151352535 | TGCAACCTCAAACTC[A/G]CGGTTCAAGCAATCC | 51667 |
rs187815865 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370206 | ATTCTTCTGCCTTAG[C/T]CTTCTAAGTAGCTGG | 51667 |
rs187891555 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151365451 | TTAGTAAAACATGAA[C/T]GAGCCTGTTAAAGCA | 51667 |
rs187947533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151366226 | CTGCCACGAATACGG[A/G]GTCAAATTTTGCCTG | 51667 |
rs187954301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349534 | GGAATAAAGGATTCC[C/G]AAGTTTCCTAGAAGC | 51667 |
rs188078005 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NUB1 | GRCh38.p7 | 7:151344631 | CGAAAATATTTATTA[A/T]CGATAGTTTACAGTT | 51667 |
rs188093285 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364345 | AGAATGGCAGGAACC[C/T]GGGAGGCGAAGCTTG | 51667 |
rs188099022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151345028 | AGAAGTTCACGACTC[A/G]AGGGATTTATCTTTC | 51667 |
rs188210270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151347876 | TACATTATGAATTTA[A/G]TGAAACCTTGACCTT | 51667 |
rs188353331 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | NUB1 | GRCh38.p7 | 7:151362451 | CCAAGTAAGCTAGAA[C/G]TTTTGTCACAACTTC | 51667 |
rs188475347 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151376279 | ATCCAGCTTTGTATC[C/G]CAAGTGACGGCTCTG | 51667 |
rs188611787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372042 | AAGTTTATATTTTTT[A/G]TGCAATATGGCCCTG | 51667 |
rs188614016 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NUB1 | GRCh38.p7 | 7:151353734 | GACCAGTTAGCTACT[A/G]CAGCCATCCATACAA | 51667 |
rs188631476 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NUB1 | GRCh38.p7 | 7:151359516 | GGGCACCGTGGCTCA[C/T]GCCTGTAATCCCAGC | 51667 |
rs188650101 | snp | C/T | | | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378164 | TAACCGTCCTCACTG[C/T]GCCACGCACTCCTCT | 51667 |
rs188669886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151342963 | ACAGGTGTGAGCCAC[C/T]GCGCCCGGCCTTGGA | 51667 |
rs188757314 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151366880 | CACAAAAAGGTTTCA[A/G]ATGCTAAAAATGTTT | 51667 |
rs188759093 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NUB1 | GRCh38.p7 | 7:151364019 | GGATGGTCTTGAACT[C/T]CTGACGTCAGGTGAT | 51667 |
rs188763535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151350336 | TCTCTAACTACCCCA[A/G]GGAGAGGCTCCCTTT | 51667 |
rs188859877 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341050 | GTACTGCACCCCATT[G/T]TACATACACACACAT | 51667 |
rs188866555 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUB1 | GRCh38.p7 | 7:151375498 | TTAAGTCTAGAGGGC[A/G]TGACGCTTTCAAAGA | 51667 |
rs188991370 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151355417 | CAAGGCCTGATGTCT[A/G]TAACCCAGCACTTTG | 51667 |
rs189150984 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NUB1 | GRCh38.p7 | 7:151356944 | CTAGTCTTGAACTCC[C/T]GACCTCAGGTGATTT | 51667 |
rs189285116 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151372648 | GATAAGGTCAGTTTC[A/G]AAGCATTGTTGGGGC | 51667 |
rs189335490 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151373657 | ACATCACATTTTAAC[C/T]TGAATCCCTGGGCGA | 51667 |
rs189429818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151367255 | TGCAGTATAGTCTTT[A/T]TAAACTATATATTTA | 51667 |
rs189569255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151366683 | CAAGGGGCTGCATGT[A/G]TGTCCTGGGGCAAGT | 51667 |
rs189610169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365096 | CCCAAAGTGCTGAGA[C/T]TACAGGTGTGAGCCA | 51667 |
rs189726341 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346558 | GCTGATGACTAATAC[A/T]AATGGTCAGTGATTT | 51667 |
rs189752402 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | NUB1 | GRCh38.p7 | 7:151362311 | TGTTAGCATATTTTT[G/T]TGTGTGTGTGATTTC | 51667 |
rs189760357 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344557 | GAACTCCTGACCTCA[G/T]CTCCTGAACTCAGCC | 51667 |
rs189821718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349898 | CCGGAGGACCACTAC[C/T]ACCTAGACGCGGAAA | 51667 |
rs189833284 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NUB1 | GRCh38.p7 | 7:151358860 | ACAAGATCAGGAGAT[C/T]GAGACCATCCTGGCT | 51667 |
rs190354568 | snp | C/T | 0.000553752 | 0.0166304 | missense | NUB1 | GRCh38.p7 | 7:151356161 | ATCCAGAAATGACAC[C/T]GTACTTAGACATAGC | 51667 |
rs190365300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151374797 | TAGGGCAGGTGCTGC[A/G]CTGCGTCTCAGCAGC | 51667 |
rs190385716 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340070 | GACTTCGCTTTCTGG[A/C]TTTTCTAGTTGTTGT | 51667 |
rs190494722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369293 | GATTACAGGTGTGAG[C/T]CACCGCGCCTGGCCG | 51667 |
rs190495011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151352313 | GTTTAAAAAGGACCT[C/T]GTCTCCTACAGTTTC | 51667 |
rs190514928 | snp | C/G/T | 0.00219384 | 0.0330484 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151377090 | CATGGAGACAGAGGC[C/G/T]GTCAATGAGATACTG | 51667 |
rs190533527 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350630 | GAGTAATACTACAAA[C/T]TAATAATGATATTCA | 51667 |
rs190626773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354480 | TTCACAATATTATTT[G/T]TTATTTTAAAATCTG | 51667 |
rs190767639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359368 | GAATGGTGTGAACCT[A/G]GGAGGTGGAGCTTGC | 51667 |
rs190816394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151367507 | CAAGAGCTGTGGCTC[A/G]AGTAAGGATTTTTCT | 51667 |
rs190847869 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151347264 | ATGTATTGCTGGACA[C/T]AGTGGCGCATGCCTG | 51667 |
rs190856110 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364908 | CATGAAAATGTAACA[A/G]TGTTGAATATTAATG | 51667 |
rs190991275 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344252 | ATCAGAAAATATGCA[A/G]AATTTTCCTAGTATT | 51667 |
rs191009686 | snp | A/G | 0.368119 | 0.220336 | intron-variant | NUB1 | GRCh38.p7 | 7:151361001 | GCTCAGGCTGATCTT[A/G]AACTCCTGGACTCAT | 51667 |
rs191142584 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341224 | TTGGGAATAGGACCT[C/T]GGAAGTAGGCAGAGC | 51667 |
rs191299001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151347978 | TTGAGAGGAGTATCC[C/T]GTAACTGAAATATTT | 51667 |
rs191371372 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151366471 | AACCACCAGGCCCAA[A/C]CCCCAGAAATTTCTG | 51667 |
rs191388805 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351363 | TTTTCTGATTTCACA[A/G]GGTAATCTCTCCAAA | 51667 |
rs191462486 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360988 | GTCTCCCTGTGTTGC[C/T]CAGGCTGATCTTGAA | 51667 |
rs191609713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151365524 | TCCTGCGAGTGGCAG[A/G]AGAGTCTTCTGTCAC | 51667 |
rs191617234 | snp | G/T | 0.0174175 | 0.0916809 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340645 | CCTGGGCATCCTCAG[G/T]TTACGTGCGAAACCT | 51667 |
rs191633095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151375326 | GACTGATGGGTCTCA[A/G]AATAGATGTGAATTA | 51667 |
rs191722239 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NUB1 | GRCh38.p7 | 7:151344089 | GGGAGGCTGAGGCAG[G/T]AGAATGGCGTGAACC | 51667 |
rs191724758 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378483 | ATTAATTTACTCAGC[C/T]TCCCCAGCTGTAGGT | 51667 |
rs191846760 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151376167 | GTGTCAGGAAGTTCT[A/C/G]TTTAGGTTTGCTGCC | 51667 |
rs191860141 | snp | C/G | 0.00795532 | 0.062565 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341489 | ATTTCCTCTTGATGG[C/G]TGGCAAACTGAGCCC | 51667 |
rs191871152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357649 | GAGTCTTACTCTGTT[C/G]CCCAGGCTGGAGTGC | 51667 |
rs191905640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151356925 | TTTCTCCATGTTGGT[C/T]AGGCTAGTCTTGAAC | 51667 |
rs191994925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151372146 | GCCAGGCCGTGAGAC[A/G]TAGCCTTCCTAAGAG | 51667 |
rs192040207 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151354115 | CAGTCTGTCCAGAGT[C/T]CCCCTTTCTATATAA | 51667 |
rs192157407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365762 | AATTAGAAATGTTGA[A/G]AGAGATGAAAATAAA | 51667 |
rs192196593 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NUB1 | GRCh38.p7 | 7:151348908 | TTTTTCCTGGCCTCT[C/G]TAAACTCCACACCTC | 51667 |
rs192197319 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151357051 | ACACAGGGTCTTGCC[C/G]TGTCACCCAGGCTGG | 51667 |
rs192334436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151371845 | ATCTCCCGGGCTCCA[A/G]TGATCCTCCTGCCAA | 51667 |
rs192595893 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151375793 | GGGTGCAGCGCCTGT[C/G]TGAATGTGTGAAGAG | 51667 |
rs192635800 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | NUB1 | GRCh38.p7 | 7:151364081 | TTACAGGTGTGAGCC[A/C]CCGCGCCTGGCCTAA | 51667 |
rs192663759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349598 | CCTTTTCCTGTTCCA[G/T]TAGAGGTCAGAGGGC | 51667 |
rs192695663 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NUB1 | GRCh38.p7 | 7:151344948 | GAGCTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 51667 |
rs192715820 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353517 | AACAGGCCCCACAAC[A/C]AAGACTTGTCCAGTC | 51667 |
rs192869470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151362592 | GGAAACATGAGGGGA[A/G]CTCAGTGTCTGGAGA | 51667 |
rs192912561 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342187 | ACTTGAATCGTAACA[C/G]TCCGAGTATACCATT | 51667 |
rs192941020 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151376577 | ACTCGTATGGCTGAC[A/G]GGGGTGGCAGAAGAG | 51667 |
rs192998717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151366753 | CTCTTTCTTTCCCCC[A/G]TTAGAAGGATGAGAT | 51667 |
rs193047159 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NUB1 | GRCh38.p7 | 7:151344903 | GAGTAGGGAGGCTGA[G/T]GCAGGGGAATTGCTT | 51667 |
rs193146130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151352557 | AAGCAATCCTCCTAC[A/C]CAAACCTCCCAAGCA | 51667 |
rs193158631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151359013 | GAGGTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 51667 |
rs193302225 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370649 | CTGCACCCATTAACT[C/T]GTCATTTAGCATTAG | 51667 |
rs199549586 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347417 | GACCCCGTCTCTAAA[A/G]GAAAAAAAAAGTATA | 51667 |
rs199588953 | in-del | -/G | 0.0295035 | 0.117819 | intron-variant | NUB1 | GRCh38.p7 | 7:151358444 | AGCAGGTGAGCAGCA[-/G]GCAAGTGAGCGTCAC | 51667 |
rs199807747 | snp | C/T | 0.000944393 | 0.0217096 | intron-variant | NUB1 | GRCh38.p7 | 7:151360115 | TATTTTAAAGTGATG[C/T]TTTTTAAATTTGTAT | 51667 |
rs199876601 | snp | C/T | 0.00108057 | 0.023219 | missense, intron-variant | NUB1 | GRCh38.p7 | 7:151374139 | AAAGAGAAGAAAAGA[C/T]GCCGCCTCGAGAACA | 51667 |
rs199914072 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358802 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 51667 |
rs199989925 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364432 | TCTCAAAAACAAAAA[A/C]AAAAAAAAACAAAAA | 51667 |
rs200003925 | snp | A/G | 0.00222717 | 0.033296 | missense | NUB1 | GRCh38.p7 | 7:151377091 | ATGGAGACAGAGGCC[A/G]TCAATGAGATACTGG | 51667 |
rs200115945 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377897 | TTTATATATATTCAG[C/G]ATTCCTCATTACAGA | 51667 |
rs200140451 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344214 | AAAAAAAAAAAAAAA[G/T]TAGATGTGCTGTTAG | 51667 |
rs200208346 | snp | A/G | 4.12448e-05 | 0.004541 | intron-variant | NUB1 | GRCh38.p7 | 7:151376595 | GGTGGCAGAAGAGGC[A/G]CCAGGGGCTGATGCT | 51667 |
rs200247928 | snp | A/T | | | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151351462 | CCGATTGCACATCAC[A/T]GGCAGAGAACTGAGG | 51667 |
rs200256258 | snp | G/T | 5.15983e-05 | 0.00507902 | intron-variant | NUB1 | GRCh38.p7 | 7:151360103 | TTTGCCTTATTATAT[G/T]TTAAAGTGATGTTTT | 51667 |
rs200512996 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357625 | TTTTTTTTTTTTTTT[C/T]TTGAAAAGGAGTCTT | 51667 |
rs200617112 | snp | G/T | 1.65679e-05 | 0.00287814 | intron-variant | NUB1 | GRCh38.p7 | 7:151375806 | GTCTGAATGTGTGAA[G/T]AGTTCTTAGTGATGG | 51667 |
rs200617813 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369152 | AGCTGGGATTACAGG[C/T]GTGTGCCACCACACC | 51667 |
rs200618731 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347418 | ACCCCGTCTCTAAAA[A/G]AAAAAAAAAGTATAT | 51667 |
rs200711078 | snp | A/G/T | 3.3502e-05 | 0.00409266 | missense | NUB1 | GRCh38.p7 | 7:151368739 | CCTGTCTCTAGGCAC[A/G/T]TCAGCTCTTTAAAGA | 51667 |
rs200735252 | snp | A/G | 0.000103824 | 0.00720426 | intron-variant | NUB1 | GRCh38.p7 | 7:151368692 | TGTATTAAGCTTTAA[A/G]TATTGCCGTGGTTAC | 51667 |
rs200776093 | snp | A/G | 0.000210291 | 0.0102519 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151351427 | TATTTTTAACAGGAT[A/G]GGAAAAACTTGTTGG | 51667 |
rs200802223 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364433 | CTCAAAAACAAAAAC[A/C]AAAAAAAACAAAAAA | 51667 |
rs200906280 | snp | C/T | 0.000305452 | 0.0123545 | intron-variant | NUB1 | GRCh38.p7 | 7:151377031 | ATTCACTTACTCCTG[C/T]GGTATTTTATTGTAG | 51667 |
rs200906783 | snp | A/G | 0.000617976 | 0.0175672 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151355877 | GTTAGAGGAAGAGGA[A/G]CAAAATGAGGCCAAA | 51667 |
rs200909680 | in-del | -/A | 0.123105 | 0.215401 | intron-variant | NUB1 | GRCh38.p7 | 7:151359776 | ATGAGACTCCGTCTC[-/A]AAAAAAATAAAATAA | 51667 |
rs201141302 | in-del | -/G | 0.0865458 | 0.189163 | intron-variant | NUB1 | GRCh38.p7 | 7:151355044 | CCACCACGCCCTGCT[-/G]GTCTTTGCTTTTAAC | 51667 |
rs201178163 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363470 | AAAAAAAAAAAAAAT[C/T]AACAGAGCATCTGCA | 51667 |
rs201314563 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | NUB1 | GRCh38.p7 | 7:151345006 | TCCGTCTCAAAAAAG[-/A]AAAAAAAGAAGTTCA | 51667 |
rs201361812 | snp | G/T | 0.000100115 | 0.00707443 | intron-variant | NUB1 | GRCh38.p7 | 7:151374048 | CAGACTGAGAGGCTG[G/T]GAAATCTCAGTCCCT | 51667 |
rs201382588 | snp | C/T | 0.000489322 | 0.015634 | intron-variant | NUB1 | GRCh38.p7 | 7:151376612 | CAGGGGCTGATGCTG[C/T]GACCCCTGCGCTCTC | 51667 |
rs201576249 | snp | C/T | 5.00455e-05 | 0.00500202 | intron-variant | NUB1 | GRCh38.p7 | 7:151355956 | GCAAAGAGAGGTACC[C/T]AGAGCTCTGGGCTTG | 51667 |
rs201670102 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356820 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 51667 |
rs201670558 | snp | A/G | 0.000184886 | 0.00961294 | missense | NUB1 | GRCh38.p7 | 7:151376667 | GATGCACTCGTGGCC[A/G]AAGCTGCGCTGAGAG | 51667 |
rs201797978 | snp | A/G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373258 | GCTTTCTGTCTCCTT[A/G/T]TTGGGAAAATAATGA | 51667 |
rs201834116 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369204 | GTAAAGATGGGGTTT[C/T]ACCATGTTGGCCAGG | 51667 |
rs201900450 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364441 | CAAAAACAAAAAAAA[A/C]CAAAAAAAAAAACAA | 51667 |
rs201964306 | snp | G/T | 3.48002e-05 | 0.00417119 | intron-variant | NUB1 | GRCh38.p7 | 7:151360126 | GATGTTTTTTAAATT[G/T]GTATTTTTTCCTAGG | 51667 |
rs202008318 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372568 | GGAGTATGTGTAAAT[-/A]AAAGTGCAAATGTGA | 51667 |
rs202096934 | snp | A/G | 0.000391529 | 0.0139861 | missense | NUB1 | GRCh38.p7 | 7:151376661 | GGTTTTGATGCACTC[A/G]TGGCCGAAGCTGCGC | 51667 |
rs202103436 | snp | C/T | 0.00152258 | 0.0275495 | intron-variant | NUB1 | GRCh38.p7 | 7:151352768 | TAATGGATAATAAAT[C/T]GCAATTTTGTTTTCC | 51667 |
rs202108670 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344213 | AAAAAAAAAAAAAAA[A/G]GTAGATGTGCTGTTA | 51667 |
rs202123795 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151348383 | GGAATATTTTCTGGG[-/T]TTTTTTTTTCATTTT | 51667 |
rs367601039 | snp | A/G | 1.78379e-05 | 0.00298641 | intron-variant | NUB1 | GRCh38.p7 | 7:151352925 | TTTAATGAACCAAAT[A/G]TAGAAATAATGACTT | 51667 |
rs367707343 | snp | C/T | 7.78649e-05 | 0.0062391 | missense | NUB1 | GRCh38.p7 | 7:151360148 | TTTCCTAGGCCCTTA[C/T]GTTAGCTATGGGATA | 51667 |
rs367708877 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375749 | CCTCATAGCAGCAGA[A/G]GACGGCGGGGTCTGC | 51667 |
rs367719318 | snp | A/G | 5.07009e-05 | 0.00503467 | intron-variant | NUB1 | GRCh38.p7 | 7:151349043 | TTTTTTTTTTAAGTC[A/G]GTATTGCATTTTCTG | 51667 |
rs367781408 | snp | C/T | 5.91453e-05 | 0.00543775 | intron-variant | NUB1 | GRCh38.p7 | 7:151376819 | CTCCGCAGGTAGGTC[C/T]GAGGTCTTTGAGGGC | 51667 |
rs367952673 | snp | G/T | 0.000117109 | 0.00765119 | intron-variant | NUB1 | GRCh38.p7 | 7:151349262 | AATTTCCCTAAATTT[G/T]AGTAGGCACTAATGT | 51667 |
rs368060289 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360922 | TATTACAGGTGTGAG[C/T]CGCTGTGTCGGCTTT | 51667 |
rs368113521 | snp | A/C | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341656 | CCACGCCCACACAAC[A/C]GTATCCCCGCCCACA | 51667 |
rs368133733 | snp | A/G | 6.79002e-05 | 0.00582628 | missense | NUB1 | GRCh38.p7 | 7:151366982 | GTGGATAACTACGCC[A/G]TCCTCCAGCTGGATA | 51667 |
rs368373075 | snp | A/G | 7.60485e-05 | 0.00616591 | missense, intron-variant | NUB1 | GRCh38.p7 | 7:151374211 | CAGCAGGTACTCCAC[A/G]CAGCCAGCGGGAACT | 51667 |
rs368526407 | snp | A/T | 0.000169986 | 0.00921759 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345404 | TTTTTAAGGGAAGAC[A/T]GGATTCAACTTTGGA | 51667 |
rs368529402 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355194 | CAATGTTCTCCCTGT[A/T]GTAGATTATCAAATA | 51667 |
rs368530826 | snp | A/C | 4.73272e-05 | 0.00486429 | missense | NUB1 | GRCh38.p7 | 7:151376797 | CGCCAGCCACGTCCC[A/C]TTCTGACTCCGCAGG | 51667 |
rs368620193 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377720 | CCCGCCCCTCAAATC[A/G]TCCTTTAAGTCTTCC | 51667 |
rs368626965 | snp | A/G | 4.96816e-05 | 0.00498381 | missense | NUB1 | GRCh38.p7 | 7:151375906 | ATCCTGAAACCGACA[A/G]CCGTCAAGAAAGTCC | 51667 |
rs368628031 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358490 | TCCTGTCAGATCAGC[A/G]GCGGCATTAGAGTCT | 51667 |
rs368630465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151345588 | AGCATTAGTGGTGAG[C/T]GGGTACCCACTTTTT | 51667 |
rs368642295 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371572 | CCACCTGGGGAGCTG[A/G]AGCAGCCTCCCACAC | 51667 |
rs368677716 | snp | A/G | 0.000169986 | 0.00921759 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151355779 | ATAGGGAAAACCCTT[A/G]AAGAACAAGGCGTGG | 51667 |
rs368835178 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151353187 | TTCTTCTTGAAGGAG[A/G]AGAGCTAAGGCTGTG | 51667 |
rs368893168 | snp | C/T | 0.000334965 | 0.0129372 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151367902 | GTTTCTAAGACTCTA[C/T]TTACTTCAAGGGATC | 51667 |
rs368918074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151362467 | TTTTGTCACAACTTC[C/T]TACCATATGTCTTGG | 51667 |
rs369047105 | snp | G/T | 0.000339748 | 0.0130291 | missense | NUB1 | GRCh38.p7 | 7:151377137 | ATGAGGAAGACTATC[G/T]TGACTCAACTCTGGA | 51667 |
rs369053040 | snp | C/G | 0.000161987 | 0.00899817 | intron-variant | NUB1 | GRCh38.p7 | 7:151356095 | TAACTGTTTAACATT[C/G]AGTTCATGGAGGTCC | 51667 |
rs369161689 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151370367 | GTGCTGGGATCACAG[G/T]TGTGAGCCACTGCGA | 51667 |
rs369282108 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364204 | GAGGCAGGCAGATCA[C/T]GAGGTCAGGAGATCA | 51667 |
rs369312974 | snp | C/T | 0.000167986 | 0.00916323 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349163 | TGCAAGGCAATTGAG[C/T]GTGGAACAGGAAATG | 51667 |
rs369377894 | snp | A/G | 4.9736e-05 | 0.00498653 | missense | NUB1 | GRCh38.p7 | 7:151368838 | TTGGCCTGAGGGCGT[A/G]TGATGGGAACGTGGA | 51667 |
rs369380781 | in-del | -/CAGGTGCACATCACCA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360775 | AGGTGCACATCACCA[-/CAGGTGCACATCACCA]TGCCCAGATAATTTT | 51667 |
rs369425733 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365385 | GAGATAAGTGCATAT[G/T]GATTTTATTTTTAAC | 51667 |
rs369461817 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343624 | TGCCTTACATCTCAG[C/T]CGCCTCACTCACCTT | 51667 |
rs369541322 | snp | C/T | 0.000461432 | 0.0151823 | intron-variant | NUB1 | GRCh38.p7 | 7:151376840 | CTTTGAGGGCCGCAT[C/T]GAGAGCAAAGTGTCT | 51667 |
rs369641442 | snp | C/T | 0.000248523 | 0.0111445 | intron-variant | NUB1 | GRCh38.p7 | 7:151375983 | CAGCTTGGACAGCCT[C/T]GGGTGGGGTTGCTTG | 51667 |
rs369681414 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350683 | ATTTCTAGTGTAACT[A/G]TTCTTATTCTATATA | 51667 |
rs369934149 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346989 | TAACGCTAACTCTGG[G/T]TAGTTAGTGTCAGAA | 51667 |
rs369943539 | snp | A/C | 6.65314e-05 | 0.00576726 | missense | NUB1 | GRCh38.p7 | 7:151368868 | ATCATGCGGCCACTC[A/C]TATTACCAACCGCAG | 51667 |
rs369981478 | snp | C/T | 7.58668e-05 | 0.00615854 | intron-variant | NUB1 | GRCh38.p7 | 7:151376604 | AGAGGCGCCAGGGGC[C/T]GATGCTGTGACCCCT | 51667 |
rs370093318 | snp | A/G/T | 0.000138523 | 0.00832121 | missense, stop-gained, intron-variant | NUB1 | GRCh38.p7 | 7:151374148 | AAAAGACGCCGCCTC[A/G/T]AGAACATCAGGTTTC | 51667 |
rs370184507 | in-del | -/GTTAGG | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371299 | AGGATAGGTCTCAGG[-/GTTAGG]TGATTCATTCAGTGG | 51667 |
rs370286597 | snp | A/G | 0.497803 | 0.033074 | intron-variant | NUB1 | GRCh38.p7 | 7:151361028 | TCATGTGATCCTCCT[A/G]CCTTGGCCTCCCAAA | 51667 |
rs370294175 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151345558 | ATGACCATATAAACT[G/T]TTGGCATAACCAAAA | 51667 |
rs370353337 | snp | C/G | 0.000169986 | 0.00921759 | intron-variant | NUB1 | GRCh38.p7 | 7:151355725 | CTGTTACCTGGTAAG[C/G]TTAATGGCTTTTTAA | 51667 |
rs370365707 | snp | C/T | 0.000142504 | 0.00843989 | intron-variant | NUB1 | GRCh38.p7 | 7:151366927 | GTGATGTCACTGTCC[C/T]TCTCTTTCCAGTGAG | 51667 |
rs370571275 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368893 | CCGCAGAGAGGTACC[C/T]ACTTTCACATGCCCT | 51667 |
rs370586827 | snp | C/T | 0.00207871 | 0.032172 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376660 | GGGTTTTGATGCACT[C/T]GTGGCCGAAGCTGCG | 51667 |
rs370626130 | snp | A/G | 0.000137344 | 0.00828571 | synonymous-codon, intron-variant | NUB1 | GRCh38.p7 | 7:151374186 | GATGGGCTACTCCAC[A/G]CACGCGGCCCAGCAG | 51667 |
rs370674897 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151371554 | CCTTAGCCCATTCAG[C/G]GGCCACCTGGGGAGC | 51667 |
rs370705202 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370625 | GTATACATGTGCCAT[A/G]CTGGTGCGCTGCACC | 51667 |
rs370811153 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | NUB1 | GRCh38.p7 | 7:151351555 | TTGATCCTCTGTGAG[C/T]GTCCTCTTAAGATAG | 51667 |
rs370940556 | snp | A/G | 0.000122988 | 0.00784083 | missense | NUB1 | GRCh38.p7 | 7:151376697 | GTGTTCAGAGGCAAC[A/G]TCCAGCTGGCCGCCC | 51667 |
rs370952148 | snp | C/T | | | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377438 | TGGCGCAGGCCGTTC[C/T]ATCTGCCTCCCAGGT | 51667 |
rs371002277 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348562 | TGTTTTTGTTTTTTG[C/T]TTTTTGCTTTTTTTT | 51667 |
rs371046404 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151365745 | TTCTCAAACATTCAC[A/G]AAATTAGAAATGTTG | 51667 |
rs371051978 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348010 | GGACTGGAAGTGTGT[C/T]TGGATTTTGGAATGT | 51667 |
rs371070382 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356261 | GCCTGTTCTTAGATT[C/T]GTTGTCAGGGCAGAG | 51667 |
rs371101574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151349495 | TCTGATCCTTTCTAG[C/T]GTGTGAACGTTGAGA | 51667 |
rs371196896 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343413 | TTCAAAGATTTCAAA[A/G]TTGTGTGAATTGGGT | 51667 |
rs371202151 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358822 | GTAATCCCAGCACTT[G/T]GGGAGGCCGAGGTGG | 51667 |
rs371257673 | snp | C/G | 3.37012e-05 | 0.00410481 | missense, splice-acceptor-variant | NUB1 | GRCh38.p7 | 7:151356130 | GGTTTTGTTACAGCA[C/G]CAGAGACAGTGGTGG | 51667 |
rs371347421 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375114 | TGGGTGCAGCAGGCA[C/T]GGGGAGTCCACCCTG | 51667 |
rs371511575 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362151 | TACAAATTTGGCTAC[A/G]TCTTCAGTTCATGAT | 51667 |
rs371625837 | snp | C/T | 8.29318e-05 | 0.00643887 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349145 | GTAATAGAAGAAATA[C/T]GTTGCAAGGCAATTG | 51667 |
rs371631312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342470 | AGTGAAATTTTTAAA[A/G]GATCGTTATAACGTT | 51667 |
rs371688340 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372444 | GTCCGCTGGCTGGCA[A/G]CGTCCTTCTCTGTGC | 51667 |
rs371691232 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354034 | GTTGAAGTCCTTTCC[C/T]TAACCCCAGGGCCAC | 51667 |
rs371700838 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340131 | TCCATCACACCTGAG[C/T]GTGGACATTCAATTT | 51667 |
rs371703710 | snp | G/T | 4.96931e-05 | 0.00498439 | intron-variant | NUB1 | GRCh38.p7 | 7:151375954 | ACCGAGTGAGTGACA[G/T]GCCTTTGTGCCCTCA | 51667 |
rs371772195 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350090 | AGAGAGGACAGCTTA[C/T]GTCATTATTTCTTCT | 51667 |
rs371804068 | in-del | -/G | | | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377375 | CAAGTCCAGGAGGGG[-/G]TCCCAGGGCCTTCAT | 51667 |
rs371877913 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371769 | TTTTGTTTGAGACAG[A/C]GCCTTGCTCTCTTGT | 51667 |
rs371909121 | snp | A/G | 1.65748e-05 | 0.00287874 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349169 | GCAATTGAGCGTGGA[A/G]CAGGAAATGACAATT | 51667 |
rs371979120 | snp | A/G | 0.000157987 | 0.00888643 | intron-variant | NUB1 | GRCh38.p7 | 7:151376821 | CCGCAGGTAGGTCTG[A/G]GGTCTTTGAGGGCCG | 51667 |
rs372112556 | snp | C/G | | | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378379 | CAGTTTGGACTGATG[C/G]GAATCTTCTTGTCAT | 51667 |
rs372135418 | snp | A/G | | | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378154 | GCTCCAGCAGTAACC[A/G]TCCTCACTGCGCCAC | 51667 |
rs372248808 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363312 | AAAGACCCACATTAG[A/G]ATGTAAGAGATGAAA | 51667 |
rs372297967 | in-del | -/A | 0.0927667 | 0.194365 | intron-variant | NUB1 | GRCh38.p7 | 7:151360310 | CAGACTATACAGAAC[-/A]CCCTGCCATGCCCTT | 51667 |
rs372328583 | snp | C/T | 1.69255e-05 | 0.00290903 | splice-donor-variant | NUB1 | GRCh38.p7 | 7:151367127 | TGGTCCACATAAAAG[C/T]ATGTTCCTGGAATTC | 51667 |
rs372366660 | snp | C/G/T | 1.69037e-05 | 0.00290716 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151366987 | TAACTACGCCGTCCT[C/G/T]CAGCTGGATATAGTG | 51667 |
rs372579673 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344150 | TGTACCACTGCACTC[C/T]AGCCTGGGCGACAGA | 51667 |
rs372703813 | snp | A/C | 0.000161987 | 0.00899817 | splice-acceptor-variant | NUB1 | GRCh38.p7 | 7:151375846 | GTTCCTGTGTGTTTT[A/C]GATTCTGCTCAGCAA | 51667 |
rs372764827 | snp | A/G | 0.000151389 | 0.00869894 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377244 | ATGAACAGAAATAGC[A/G]CTAATTTTCTGCTTA | 51667 |
rs372768925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358008 | GTGAGGCGGAGTCTC[A/G]CTCTGTCATCAGGCT | 51667 |
rs372775125 | snp | C/T | 0.0002513 | 0.0112066 | missense | NUB1 | GRCh38.p7 | 7:151376806 | CGTCCCCTTCTGACT[C/T]CGCAGGTAGGTCTGA | 51667 |
rs372865814 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349037 | TGCCTTTTTTTTTTT[-/T]AAGTCAGTATTGCAT | 51667 |
rs372884538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151347651 | TTTTTGTAGAGACGG[A/G]GTTTCACTTTGTTGC | 51667 |
rs372920157 | snp | C/T | 0.000169986 | 0.00921758 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345428 | CTTTGGAAACCTCCA[C/T]ATACAGATGAAAATA | 51667 |
rs373067932 | snp | C/T | 1.66927e-05 | 0.00288895 | intron-variant | NUB1 | GRCh38.p7 | 7:151355970 | CCAGAGCTCTGGGCT[C/T]GTCACCCACTCAGCT | 51667 |
rs373177200 | snp | C/T | 4.46279e-05 | 0.00472355 | missense | NUB1 | GRCh38.p7 | 7:151377185 | TTGCAGAGTACCTAT[C/T]CTATGTAGAAAATAG | 51667 |
rs373230622 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359019 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 51667 |
rs373230911 | snp | A/G | 0.000845105 | 0.0205387 | intron-variant | NUB1 | GRCh38.p7 | 7:151375988 | TGGACAGCCTCGGGT[A/G]GGGTTGCTTGGGGTA | 51667 |
rs373249445 | snp | A/G | 0.00035397 | 0.0132989 | intron-variant | NUB1 | GRCh38.p7 | 7:151352769 | AATGGATAATAAATC[A/G]CAATTTTGTTTTCCT | 51667 |
rs373332059 | in-del | -/CACAGGTGCACATCAC | 0.0271762 | 0.113356 | intron-variant | NUB1 | GRCh38.p7 | 7:151360757 | CTAAGTAGCTGGGAT[-/CACAGGTGCACATCAC]CACAGGTGCACATCA | 51667 |
rs373388410 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355341 | ACCAAATGTAGGCAT[A/G]TTTTTACCAATTATG | 51667 |
rs373447261 | snp | C/T | 0.00106763 | 0.0230798 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151377103 | GCCGTCAATGAGATA[C/T]TGGAAGACATTCCAG | 51667 |
rs373576077 | snp | A/G | 0.000116784 | 0.00764057 | missense | NUB1 | GRCh38.p7 | 7:151367919 | TACTTCAAGGGATCC[A/G]AAACTATCACAGTGG | 51667 |
rs373585318 | snp | A/T | 3.5766e-05 | 0.00422868 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345435 | AACCTCCATATACAG[A/T]TGAAAATAAAAAAGT | 51667 |
rs373605778 | snp | A/G/T | 9.96552e-05 | 0.00705824 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368860 | GAACGTGGATCATGC[A/G/T]GCCACTCATATTACC | 51667 |
rs373655646 | snp | C/T | 0.497749 | 0.0334707 | intron-variant | NUB1 | GRCh38.p7 | 7:151361032 | GTGATCCTCCTGCCT[C/T]GGCCTCCCAAAGTGC | 51667 |
rs373725093 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370768 | CTCATTGTTCAATTC[C/T]CACCTGTGAGTGAGA | 51667 |
rs373793040 | snp | C/T | 8.61913e-05 | 0.00656416 | intron-variant | NUB1 | GRCh38.p7 | 7:151356102 | TTAACATTGAGTTCA[C/T]GGAGGTCCTTTTGGT | 51667 |
rs373809304 | snp | G/T | 6.75333e-05 | 0.00581052 | synonymous-codon, intron-variant | NUB1 | GRCh38.p7 | 7:151374171 | CAGGTTTCTGAAAGG[G/T]ATGGGCTACTCCACG | 51667 |
rs373816507 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375007 | TGGCTTAGGTTGTGC[A/G]CGTGCTGGGGGCGGG | 51667 |
rs373895352 | snp | C/T | 3.32563e-05 | 0.00407763 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151367092 | CTTTAAAAATTGTTA[C/T]GGAGAAAATCATCAG | 51667 |
rs373920433 | snp | A/T | 1.67464e-05 | 0.0028936 | intron-variant | NUB1 | GRCh38.p7 | 7:151349266 | TCCCTAAATTTGAGT[A/T]GGCACTAATGTCCAG | 51667 |
rs373953124 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367684 | AGGAATGTTATCATA[C/T]CACAGGGGATGGGGA | 51667 |
rs374103313 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357280 | AGGCACGCACCACCA[C/T]GCCTGGCTAACTTTT | 51667 |
rs374234954 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347748 | ACAGGCATGAGCCAT[C/T]GCGCCCAATCTATAC | 51667 |
rs374431711 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373701 | GGAAGGCCTTCCCAC[C/T]GCGTGCAGAAGCTCT | 51667 |
rs374602389 | in-del | -/AA/AGTT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363756 | ACCTTTCTTGAAAAA[-/AA/AGTT]AGTTAGGTAAGTTTG | 51667 |
rs374673411 | snp | A/G | 0.000102596 | 0.00716152 | missense | NUB1 | GRCh38.p7 | 7:151376808 | TCCCCTTCTGACTCC[A/G]CAGGTAGGTCTGAGG | 51667 |
rs374850587 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151354418 | TTTCTCAAAAGAAAA[A/T]AATCCAGCTAGTTTT | 51667 |
rs374932407 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358883 | TCCTGGCTAACACAA[C/T]GAAACCCCATCTCTA | 51667 |
rs374955747 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343554 | ATAACATTTTTCTTT[A/G]CTTATTGCTTGTCTG | 51667 |
rs374957765 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364041 | TCAGGTGATCCGTCC[A/G]CCTCAGCCTCCCAAA | 51667 |
rs375032507 | snp | C/T | 0.000301432 | 0.0122729 | synonymous-codon, intron-variant | NUB1 | GRCh38.p7 | 7:151374210 | CCAGCAGGTACTCCA[C/T]GCAGCCAGCGGGAAC | 51667 |
rs375046211 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365638 | TCAAAGGCAGGTTCT[C/T]AGGCTGAGCCGTAGA | 51667 |
rs375054725 | snp | C/T | 6.30272e-05 | 0.00561334 | missense | NUB1 | GRCh38.p7 | 7:151355846 | AATCTGAAGAGGACG[C/T]GAGGAAAAACTTCCA | 51667 |
rs375064982 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354609 | CTTTTGATTTTGTTA[A/C]TGTTTTCTTTCATTC | 51667 |
rs375120985 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340230 | GAAAAAAATGTCAGA[A/G]CAGTTTCTGTTGTCC | 51667 |
rs375136794 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362620 | AGAAGTTTCAGGTTA[C/T]GGGGCAGGGAGGGCA | 51667 |
rs375215823 | snp | A/G | 0.000194824 | 0.00986783 | intron-variant | NUB1 | GRCh38.p7 | 7:151376829 | AGGTCTGAGGTCTTT[A/G]AGGGCCGCATTGAGA | 51667 |
rs375249180 | snp | C/T | 0.000298235 | 0.0122077 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349194 | ACAATTATAGAACAA[C/T]GGGAATTGCTACAAT | 51667 |
rs375297631 | in-del | -/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364453 | AAACAAAAAAAAAAA[-/C]CAAAAAAACTGTAAG | 51667 |
rs375419224 | in-del | -/CA | 0.0146672 | 0.084371 | intron-variant | NUB1 | GRCh38.p7 | 7:151350897 | GTGGTCTATTCATAC[-/CA]GATGGAAAACTGTTC | 51667 |
rs375598737 | snp | A/T | 1.71563e-05 | 0.0029288 | intron-variant | NUB1 | GRCh38.p7 | 7:151352898 | GTATGTATGGCAAAG[A/T]ATGCATAATTTTTTA | 51667 |
rs375604077 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348554 | CAAATAAATGTTTTT[G/T]TTTTTTGCTTTTTGC | 51667 |
rs375619382 | snp | A/G | 7.17489e-05 | 0.0059891 | missense, intron-variant | NUB1 | GRCh38.p7 | 7:151374140 | AAGAGAAGAAAAGAC[A/G]CCGCCTCGAGAACAT | 51667 |
rs375656936 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371563 | ATTCAGGGGCCACCT[A/G]GGGAGCTGGAGCAGC | 51667 |
rs375721799 | snp | C/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339709 | CCCTAGCAGATCTCA[C/G]ACTCGAATCTTTGTT | 51667 |
rs375774682 | snp | C/G | 0.000105826 | 0.00727335 | missense | NUB1 | GRCh38.p7 | 7:151377106 | GTCAATGAGATACTG[C/G]AAGACATTCCAGAGC | 51667 |
rs375777780 | snp | A/G | 8.69074e-05 | 0.00659137 | missense | NUB1 | GRCh38.p7 | 7:151376730 | ACCCTTGCTCACAAC[A/G]GAGGAAGCCTGCCTC | 51667 |
rs375822133 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369907 | AGCCCCGTGGTTGTT[-/T]GCCTACCTGATGCCA | 51667 |
rs375824228 | in-del | -/TAGATGT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344214 | AAAAAAAAAAAAAAG[-/TAGATGT]TAGATGTGCTGTTAG | 51667 |
rs376083985 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354126 | GAGTCCCCCTTTCTA[C/T]ATAAAGTTTAAGGGT | 51667 |
rs376189202 | snp | A/G | 1.65803e-05 | 0.00287922 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349153 | AGAAATACGTTGCAA[A/G]GCAATTGAGCGTGGA | 51667 |
rs376207252 | snp | C/T | 0.000186266 | 0.00964875 | intron-variant | NUB1 | GRCh38.p7 | 7:151376621 | ATGCTGTGACCCCTG[C/T]GCTCTCCCCTAGTTG | 51667 |
rs376361966 | snp | A/C/T | 0.000163987 | 0.00905352 | intron-variant | NUB1 | GRCh38.p7 | 7:151375968 | AGGCCTTTGTGCCCT[A/C/T]AGCTTGGACAGCCTC | 51667 |
rs376372800 | snp | A/G | 5.20368e-05 | 0.00510056 | intron-variant | NUB1 | GRCh38.p7 | 7:151367155 | TTCATCTTATGTCTC[A/G]TTGAGTCCATTTCTA | 51667 |
rs376407507 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357906 | TGAGCCACTGCGCCC[A/G]GCCGGATTAAAGTTG | 51667 |
rs376418207 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151345228 | AAACCATAGTAATTT[A/G]TATTTAATGACAGAG | 51667 |
rs376523969 | snp | A/C | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341635 | CGCGGCTCCGCCCCG[A/C]GGTAACCACGCCCAC | 51667 |
rs376679280 | snp | A/C/G/T | 4.96911e-05 | 0.00498434 | missense | NUB1 | GRCh38.p7 | 7:151375942 | AGGAAAACATTGACC[A/C/G/T]AGTGAGTGACAGGCC | 51667 |
rs376680223 | in-del | -/G | 0.0325976 | 0.123435 | intron-variant | NUB1 | GRCh38.p7 | 7:151364349 | GGCAGGAACCCGGGA[-/G]GGCGAAGCTTGCAGT | 51667 |
rs376686919 | snp | A/T | 6.68181e-05 | 0.00577967 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151355928 | GAGGACCAAGAGAGG[A/T]CTAGAAATACTGGCA | 51667 |
rs376758589 | snp | C/T | 1.66167e-05 | 0.00288237 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368863 | CGTGGATCATGCGGC[C/T]ACTCATATTACCAAC | 51667 |
rs376804754 | snp | C/T | 0.00013825 | 0.00831301 | intron-variant | NUB1 | GRCh38.p7 | 7:151368699 | AGCTTTAAGTATTGC[C/T]GTGGTTACATGATTC | 51667 |
rs376805078 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374570 | CACGGCAGAAAAAAG[A/G]GAATGGGAATTCAAC | 51667 |
rs377044380 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356250 | AGAAATGTGTGGCCT[G/T]TTCTTAGATTTGTTG | 51667 |
rs377088474 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365890 | GACAAAATTAAAGTC[C/T]TTTTTTTTTTATTCC | 51667 |
rs377161931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343956 | GGAGGCCGAGGCGGG[C/T]GGATCACAAGGTCAG | 51667 |
rs377172702 | snp | C/T | 0.000686153 | 0.0185096 | missense, intron-variant | NUB1 | GRCh38.p7 | 7:151374185 | GGATGGGCTACTCCA[C/T]GCACGCGGCCCAGCA | 51667 |
rs377248707 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344232 | GATGTGCTGTTAGGC[C/T]GTTAATCAGAAAATA | 51667 |
rs377351954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151343985 | AGGAGATTGAGACCA[C/T]CCTGGCCAACACGGT | 51667 |
rs377374800 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359599 | CCTGGCCAACATGGT[A/G]AAACCCCATCTCTAC | 51667 |
rs377523756 | snp | A/G | 3.93724e-05 | 0.00443674 | intron-variant | NUB1 | GRCh38.p7 | 7:151351513 | CTCTGTGTCCTAGGT[A/G]CTCTGGGCCTTTTTA | 51667 |
rs377539725 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375093 | TTTGCCCTGCTGAGG[C/T]GGGTGTGGGTGCAGC | 51667 |
rs377552432 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375216 | TATATTTAACATATA[C/T]GTTAAATTTTAAATT | 51667 |
rs377557218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151343170 | CTAACGCTCTAAGTA[C/T]TAATATGCTTTGCTG | 51667 |
rs377643951 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348561 | ATGTTTTTGTTTTTT[G/T]CTTTTTGCTTTTTTT | 51667 |
rs386719435 | multinucleotide-polymorphism | AG/GA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360995 | TGTGTTGCTCAGGCT[AG/GA]TCTTGAACTCCTGGA | 51667 |
rs386719436 | multinucleotide-polymorphism | CA/TG | | | intron-variant | NUB1 | GRCh38.p7 | 7:151361000 | TGCTCAGGCTGATCT[CA/TG]AACTCCTGGACTCAT | 51667 |
rs386719437 | multinucleotide-polymorphism | ACCCACCACA/TCCTGCCTTG | | | intron-variant | NUB1 | GRCh38.p7 | 7:151361024 | GGACTCATGTGATCC[ACCCACCACA/TCCTGCCTTG]GCCTCCCAAAGTGCT | 51667 |
rs386719438 | in-del | AGAACG/CA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151366542 | GAAAGAAAGAAAGAA[AGAACG/CA]TTGCTCTGGCCCAGG | 51667 |
rs397726356 | in-del | -/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151365900 | AGTCCTTTTTTTTTT[-/T]ATTCCATGCATATTT | 51667 |
rs397889285 | in-del | -/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368321 | GGGCAAGAGAGAGTC[-/C]AGAGCAGGCCACTGG | 51667 |
rs397945466 | in-del | -/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371369 | TTACCCCCACCCCCC[-/C]ACCCCATGTCATCAG | 51667 |
rs397957771 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359455 | TCAAAAAAAAAAAAA[-/A]GAATAGAAAGTGAAA | 51667 |
rs397964963 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347427 | TAAAAGAAAAAAAAA[-/A]GTATATATAGGTTTA | 51667 |
rs398006759 | in-del | -/A | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151356728 | CTCCGTCTCAAAAAC[-/A]AAAAAACAAACAAAA | 51667 |
rs527288585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151360532 | TAAAGTTTCCTGTCA[G/T]CTTTTCACCTAATGG | 51667 |
rs527324016 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151354249 | TTTTCTGTTCTTCCT[A/G]CTCACCTGTGGTGTT | 51667 |
rs527358303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151367645 | GAGGCTGGTGCCCTG[A/T]CACTGACTCTCCTGT | 51667 |
rs527447137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342703 | GGTTTAATTTTTTTT[A/T]AACATTAAATCTTAT | 51667 |
rs527611403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151347444 | TATATATAGGTTTAT[C/G]TTACTTACAAAATTT | 51667 |
rs527671614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369093 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAA | 51667 |
rs527710982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151361153 | TTATATGTGGAGGTA[A/C]AATTTGTATAGGAAA | 51667 |
rs527841340 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363094 | AAAATATCCAGCATC[C/T]ACTGAAAAATTAGCA | 51667 |
rs528109970 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377380 | TCCAGGAGGGGTCCC[A/G]GGGCCTTCATGCGTG | 51667 |
rs528164303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343919 | AGGCGCGGTGGCTCA[C/G]GCCTGTAATCCCAGC | 51667 |
rs528341022 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151370915 | CACTGTATAAGACTA[C/T]AGTTCATAAAACATT | 51667 |
rs528519187 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353547 | CCCAGATGTCAGTAG[C/G]GCAGCTGTTGGGAAA | 51667 |
rs528530141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357506 | GTAGCTTCTTATAAT[A/G]AATGACTATGGGTCA | 51667 |
rs528564679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151350519 | ACTTGTCTTCTGGTC[A/G]CTTCTCACTGTGTCC | 51667 |
rs528625401 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376304 | GCTCTGTCCACATTT[A/G]TGCCCCTACACGCGT | 51667 |
rs528808624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151344871 | CGGGCGTGGTGGCGC[A/G]TGCCTGTAATCCCAG | 51667 |
rs528815334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151343333 | TGTCCCCGCACTGAC[A/G]TAAAATAGATTTGAA | 51667 |
rs529065371 | snp | C/T | 4.48823e-05 | 0.004737 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151377198 | ATCCTATGTAGAAAA[C/T]AGGAAGTCAGCAACA | 51667 |
rs529169633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343900 | AGATTTGAATAGTAG[A/G]GCCAGGCGCGGTGGC | 51667 |
rs529282245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357467 | GAACTTGGACTCTAA[A/G]ATCAATCTCTGAGAA | 51667 |
rs529283247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151356997 | GCTGGGATTACAGGC[A/G]TGAGCCACCGAACTC | 51667 |
rs529314340 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358214 | CTTGACCTCGTGATC[C/T]GCCTGCCTCGGCCTC | 51667 |
rs529357207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151356387 | GAGCACTGGCATCCA[A/G]TGGGCCTCACCCTGT | 51667 |
rs529511860 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151363613 | CAGTTTGATGAAAAC[-/TA]TAAACCCCCAGATGC | 51667 |
rs529552343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344566 | ACCTCAGCTCCTGAA[C/G]TCAGCCTCCCAAAGT | 51667 |
rs529598699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151350949 | CTGATGCGTCCACAA[C/T]GTGGGTGCACCTGAA | 51667 |
rs529644221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372485 | GGTGCGCTTCTTAGC[C/T]TTTTGGAATATAAAT | 51667 |
rs529717114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151373014 | CTGCTCCTACTGTGG[G/T]GCCTGTGGAGTCTGG | 51667 |
rs529734937 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369385 | TGCTGTGGTGGCAAA[C/T]GGTCCCCTCTCTCTC | 51667 |
rs529736813 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NUB1 | GRCh38.p7 | 7:151344176 | ACAGAGTGAGACTCC[C/G]TCTCAAAAAAAAAAA | 51667 |
rs529738715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151364780 | CTCGGCCTCCCAAAG[G/T]GCTGGGATTACAAGC | 51667 |
rs529795622 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378467 | GTCACCCTAATTTTG[C/T]ATTAATTTACTCAGC | 51667 |
rs529912734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358817 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 51667 |
rs529983372 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372100 | AAGCAACAGCTGTAG[A/G]AACGGAGCTCACAGA | 51667 |
rs530164602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151345001 | CGAGACTCCGTCTCA[A/G]AAAAGAAAAAAAGAA | 51667 |
rs530374847 | snp | C/T | 0.00015991 | 0.00894034 | synonymous-codon, intron-variant | NUB1 | GRCh38.p7 | 7:151374219 | ACTCCACGCAGCCAG[C/T]GGGAACTTGGATGAG | 51667 |
rs530454634 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347881 | TATGAATTTAATGAA[A/T]CCTTGACCTTTAGGG | 51667 |
rs530509935 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151372846 | GTAATGGGGGCATGA[A/G]ACAGGCCTGGTGCAG | 51667 |
rs530535663 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NUB1 | GRCh38.p7 | 7:151371895 | ATTTTTTTGTAGAAA[C/T]GGGGTCTCACCATGT | 51667 |
rs530645295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344435 | CCTGCCTCAGTCTCC[C/T]GAGTAGCTGGGATTA | 51667 |
rs530682126 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151369667 | GAAAGAACTGAGGTC[A/T]AGAGGGCGGTCATGG | 51667 |
rs530715861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151364588 | GGAGTGCAATGGCAC[C/G]ATCTCGGCTCACTGC | 51667 |
rs530757092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365392 | GTGCATATTGATTTT[A/G]TTTTTAACTGACATG | 51667 |
rs530876399 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151351556 | TGATCCTCTGTGAGC[G/T]TCCTCTTAAGATAGG | 51667 |
rs530887234 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NUB1 | GRCh38.p7 | 7:151351002 | CCAGACACAAAAGGC[C/T]ACGTACTGCACTATC | 51667 |
rs531031165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151373931 | TCTGCCTCTGTGGCA[C/T]CTCTGCCATTTGGCT | 51667 |
rs531039645 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151352298 | GCAGTAAAACGGAAA[C/G]TTTAAAAAGGACCTT | 51667 |
rs531071238 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347179 | AATATAAAGAATGTA[C/T]TTTTAAAATATGTTA | 51667 |
rs531164891 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151361738 | AGTCCCAACTTTAAC[A/G]TACACAAAAAAGGAA | 51667 |
rs531203057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359392 | AGCTTGCAGTGAGTC[A/G]AGATCGCGCCACTGC | 51667 |
rs531492364 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341084 | TATATACTATATATA[C/T]ACACACACTTCATTT | 51667 |
rs531541762 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151361623 | GTTAACTTCTTTTCT[G/T]TTTTGGTGCATTCCC | 51667 |
rs531602897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151353451 | GGGAGGTTGTGCTGC[C/T]GTCATTTAGTGGGTG | 51667 |
rs531629840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376100 | TCAGAGGCCACCCAC[A/G]CAGTAACAGAGGGCA | 51667 |
rs531714783 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151375752 | CATAGCAGCAGAGGA[C/T]GGCGGGGTCTGCCTA | 51667 |
rs531757479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151368068 | GACTTGTGAGAAACA[A/T]GCCTGTGCTTTCTCC | 51667 |
rs531861985 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341634 | TCGCGGCTCCGCCCC[A/G]CGGTAACCACGCCCA | 51667 |
rs531866567 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358609 | TAGAATGTTTTCACC[A/C]TGAAACCATCTGCCT | 51667 |
rs531966032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151355216 | TATCAAATATCTGTT[A/G]CTTTGATCTGGTCTT | 51667 |
rs531971169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151373819 | AGCCCATCCTGATGC[C/T]GGATGGTGGATGGCG | 51667 |
rs531975106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151361905 | TAGGTCCTAAAAGTT[G/T]AGGTAAATTTTTCAT | 51667 |
rs531999891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365649 | TTCTCAGGCTGAGCC[A/G]TAGATTTGGAGAAAG | 51667 |
rs532002403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369072 | GAGTGCAGTGGCACG[A/G]TCTTGGCTCACTGCA | 51667 |
rs532161007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151366343 | GAATGCCTTGTCAGA[A/G]CCGTCATCAGCTGAG | 51667 |
rs532307162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151345822 | ATTCTCGGTCCTCCT[G/T]GCTATCATCATCTGC | 51667 |
rs532385487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151353314 | GTGTGGCTGTGTGTG[A/G]AGAATGAGGGGAGGG | 51667 |
rs532523014 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340269 | TGCTGCAATTGCTAC[G/T]GAGCAATCAACGGGC | 51667 |
rs532625791 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341010 | GTGTCCCAAGACCCA[C/T]AGTGGATGCCTGAAA | 51667 |
rs532678499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346501 | GATTAGACACTTGAA[A/T]CTTTCCACCCTCCCC | 51667 |
rs532804778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151375502 | GTCTAGAGGGCATGA[C/T]GCTTTCAAAGATCAA | 51667 |
rs532828498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354423 | CAAAAGAAAAAAATC[C/G]AGCTAGTTTTCCAGA | 51667 |
rs533044853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343267 | GCAGCCTCATTGGCT[G/T]TGTTATTCCTTCCTC | 51667 |
rs533149764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151370632 | TGTGCCATGCTGGTG[C/T]GCTGCACCCATTAAC | 51667 |
rs533201049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151362844 | CATGAAAGAAGCAGG[A/G]AATAATCCTCCGAGT | 51667 |
rs533209457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369790 | GCCATAGAAGTCTCT[A/G]GAATCTTCACATGTA | 51667 |
rs533279553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342759 | TGCTCCCTGGAGTGT[C/G]TGACACGCACTGGGT | 51667 |
rs533324376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151358954 | CCTGTAGTCCCAGGT[A/G]CTCGGGAGGCTGAGG | 51667 |
rs533349900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151362575 | CGGTGACCCTGAGGT[A/T]GGGAAACATGAGGGG | 51667 |
rs533355484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151362191 | TGTCCGGTAAGTGGT[A/G]GGTATAATAATGAAA | 51667 |
rs533407078 | snp | A/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340172 | TACTACGTAAATGTA[A/T]AAGTGAAACTATCTT | 51667 |
rs533519108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346691 | CAACTCCATGGGACA[A/G]AGGCTTCTATGCTCA | 51667 |
rs533524293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343976 | CACAAGGTCAGGAGA[C/T]TGAGACCATCCTGGC | 51667 |
rs533606313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151350346 | CCCCAGGGAGAGGCT[C/T]CCTTTCCCAGTCTGC | 51667 |
rs533680578 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151357395 | TCCCGAAGTTCTGGG[A/T]TTACAGGTGTGAGCC | 51667 |
rs533745901 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340632 | CATGCTTGGTTCACC[C/T]GGGCATCCTCAGGTT | 51667 |
rs533784071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346113 | TGAACATGATGTAAC[A/C]TTTATCAGGGACTAA | 51667 |
rs533989237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151368245 | GAGCAGTGAGCAGCC[C/T]GCCAGCCTCAGCGAG | 51667 |
rs534006709 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | NUB1 | GRCh38.p7 | 7:151367412 | CTGACTTCTTTATAT[A/C]GGTAGAGTCTAATTT | 51667 |
rs534130744 | snp | C/T | 0.145305 | 0.227022 | intron-variant | NUB1 | GRCh38.p7 | 7:151348569 | GTTTTTTGCTTTTTG[C/T]TTTTTTTTTTTTTTT | 51667 |
rs534206670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151359265 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 51667 |
rs534236477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151360301 | AAGATGGCCCAGACT[A/G]TACAGAACACCCTGC | 51667 |
rs534335732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369951 | TTCGTGGGTTCATTC[C/T]GTGGTGAGCAGTCAC | 51667 |
rs534500211 | snp | C/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151356659 | ATACTCTTTCCCTGT[C/T]CTATAATTTGGGATA | 51667 |
rs534505534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342029 | AGCGGTGGGCCGGGC[C/T]TCGGGACGCGCTGGC | 51667 |
rs534524740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342912 | ACTCCTGACCTCAGG[C/T]GATCCACTGGCCTCG | 51667 |
rs534535903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349535 | GAATAAAGGATTCCC[A/G]AGTTTCCTAGAAGCC | 51667 |
rs534586663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369386 | GCTGTGGTGGCAAAC[A/G]GTCCCCTCTCTCTCT | 51667 |
rs534644889 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367283 | TTATAAAGTGTTCAA[C/T]GTTTTACAAATCTGG | 51667 |
rs534664770 | in-del | -/GTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCAAGGCG | 0.030665 | 0.119967 | intron-variant | NUB1 | GRCh38.p7 | 7:151359507 | AAGCAGCCGGGCACC[lengthTooLong]GTGGCTCACGCCTGT | 51667 |
rs534698890 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377573 | CTGGGAAGGGTGTCC[C/T]GACCGCTTCCTCTCC | 51667 |
rs534752734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376332 | CGTTAGCACGCCTGT[A/C]TGCTGTGGCCACTGA | 51667 |
rs534806825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151363037 | AACTTACCGTTTTCA[A/G]ATAAGTGCATCCCTA | 51667 |
rs534886625 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151372052 | TTTTTGTGCAATATG[G/T]CCCTGAGTACAGACC | 51667 |
rs535170861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151342864 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 51667 |
rs535204018 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151341999 | AGCTGGGCCGGGGCC[A/G]GGGCCGGGGCCGGGA | 51667 |
rs535231168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151372432 | GGTAATGCCCAGGTC[C/T]GCTGGCTGGCAGCGT | 51667 |
rs535253256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151369897 | GGAGCAGGAAAGCCC[C/T]GTGGTTGTTTGCCTA | 51667 |
rs535403775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151375996 | CTCGGGTGGGGTTGC[C/T]TGGGGTAACCCGGGT | 51667 |
rs535477518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349498 | GATCCTTTCTAGCGT[A/G]TGAACGTTGAGAAAT | 51667 |
rs535644537 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377463 | CCAGGTCTGCGTCCC[C/T]AACCCCTTCCCCAGC | 51667 |
rs535683070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151371277 | TACTTGTAAAAAGTC[C/T]AGAAGTAGGATAGGT | 51667 |
rs535875601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349928 | ACCGGTAGTGGCCCC[A/G]AATGCCTGGCTGTGC | 51667 |
rs536118454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151350764 | ACCTGGGTGGCTTGC[C/T]GCCCACATATATATT | 51667 |
rs536184311 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151344042 | AAAAATCAGCCGGGC[G/T]TGGTGGCGGGCGCCT | 51667 |
rs536196080 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346787 | ACTATATTCATAAGT[A/G]TACCATTTTCTGGAG | 51667 |
rs536242169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151364151 | AGCCTGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 51667 |
rs536276419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151357807 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGAC | 51667 |
rs536394847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151372015 | ACCCAGCCTTTAATA[C/T]ATAATTATTAAAAGT | 51667 |
rs536398389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151363386 | GCAGAATAGACACTA[C/T]AGAAGAGAAGATTAG | 51667 |
rs536412805 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151344914 | CTGATGCAGGGGAAT[G/T]GCTTGAACCCAGGGG | 51667 |
rs536435230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151359051 | GCCTGGAAGACAGAG[C/T]GAGACTCTGTCTCAA | 51667 |
rs536470763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151352569 | TACCCAAACCTCCCA[A/T]GCAGCTAGGGCCACA | 51667 |
rs536511220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358377 | CAGGGGTTCCCACCC[C/G]ACAGGCTGCAGATGG | 51667 |
rs536800320 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344779 | CCAAGGTGGGTGGAT[C/T]ACTTGAGGTCAGGAA | 51667 |