SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3117 | snp | C/T | 0.425277 | 0.178263 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874510 | AATTAGCCCTAAATG[C/T]GGGTAATATTTTTCC | 1161 |
rs158570 | snp | A/G | 0.468047 | 0.122292 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929087 | AAAATCTATAAATAC[A/G]TTAGGATGTGTGGTA | 1161 |
rs158571 | snp | A/G | 0.468949 | 0.12067 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940909 | TGCATATAAAGAACC[A/G]TGAAAATTTCAACTT | 1161 |
rs158572 | snp | A/G | 0.424968 | 0.178567 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943616 | tacagattaaaagag[A/G]aaattggccaaaaga | 1161 |
rs158918 | snp | A/T | 0.232359 | 0.249377 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946294 | TTTCAAGTGAGGATG[A/T]TGAGACTTGGAGAGG | 1161 |
rs158919 | snp | A/C | 0.425123 | 0.178415 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946119 | TTTCAATGGACAGCA[A/C]CGCCTCCTTACTCCC | 1161 |
rs158920 | snp | C/T | 0.312123 | 0.242158 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945441 | GGCTCTCACTTTTCC[C/T]TCCTTTACTGACCTC | 1161 |
rs158921 | snp | C/T | 0.461497 | 0.1333 | ERCC8, NDUFAF2 | 5 | allele_origin=T(germline)/C(germline) | 5:60945315 | CGTGCCCACGTGCTC[C/T]TTCACTTCCCTTGAC | 1161 |
rs158922 | snp | C/T | 0.399432 | 0.200425 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945159 | GGCGGAGAAGTCAGG[C/T]CGGCCTCCATCCTGG | 1161 |
rs158927 | snp | A/G | 0.411578 | 0.190768 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933439 | ggccaggctggtctc[A/G]aactcctgactgcag | 1161 |
rs158928 | snp | C/T | 0.256897 | 0.249905 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932096 | CAGAGGTAAGCTTTC[C/T]CACTTAGTATGGGAT | 1161 |
rs158929 | snp | C/T | 0.425123 | 0.178415 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930214 | tcgaactcctcacct[C/T]aggtgatccgcccac | 1161 |
rs158930 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929696 | ATAAAATATCAGAAA[C/T]GTCATTTGTCTTAGT | 1161 |
rs158931 | snp | C/G | 0.425123 | 0.178415 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943871 | gtgttttttttgcca[C/G]tgtcacttcctctga | 1161 |
rs158932 | snp | C/G | 0.425123 | 0.178415 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942869 | CATATCAGTGTTCAT[C/G]CTTTTGCTCTTACAT | 1161 |
rs158933 | snp | A/G | 0.468949 | 0.12067 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942763 | ttcatcaaattgtat[A/G]ttctcatttaatgtg | 1161 |
rs158934 | snp | A/T | 0.468949 | 0.12067 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942425 | tcgacaagtgactag[A/T]taaactgtggtatat | 1161 |
rs158935 | snp | C/T | 0.425123 | 0.178415 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942157 | taaataatgttcaaa[C/T]agtcaaatgaaagca | 1161 |
rs158936 | snp | A/G | 0.165289 | 0.235211 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941944 | ATATaatgtatgtaa[A/G]tataaaatataagac | 1161 |
rs158937 | snp | C/T | 0.232651 | 0.249397 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940379 | aaacaacagggattg[C/T]ccctaccctcttggg | 1161 |
rs158938 | snp | C/T | 0.41141 | 0.19091 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939413 | TCTTTGTGCTAAGGT[C/T]CATAGAAATATTTTA | 1161 |
rs162228 | snp | A/G | 0.425123 | 0.178415 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930759 | TTACTGTTTGTCTGG[A/G]TATTTAAACCTAAGG | 1161 |
rs167037 | snp | C/G | 0.00503775 | 0.0499349 | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904824 | TTGGTGGAGACTGGA[C/G]ACATATGATGACTAT | 1161 |
rs169663 | snp | C/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881455 | tatgccgtgccccca[C/G]aggtgaagtctacag | 1161 |
rs169664 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881866 | cgctgcacccactgt[C/G]ctgcacccactgtcc | 1161 |
rs182327 | snp | G/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878660 | tagtttatttgcata[G/T]aggtgtttatagtat | 1161 |
rs182352 | snp | A/T | 0.411242 | 0.191052 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939487 | AAGTTATCTAAAAAT[A/T]AAAAAAAAGAAGTAT | 1161 |
rs184091 | snp | C/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891710 | TTCTGTTGTAAAACA[C/G]AGTAGGGGTTAAATA | 1161 |
rs185975 | snp | G/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878368 | caggctttggtatca[G/T]gatgatgctgacctc | 1161 |
rs185976 | snp | C/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891804 | TCCCCAACTATGTGT[C/T]TTTGCCTCCCACTGT | 1161 |
rs186008 | snp | G/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938804 | TTCCTCCATATATAT[G/T]TAGCTTTATATAATG | 1161 |
rs188297 | snp | C/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881853 | ctcatgctcagtgcg[C/G]tgcacccactgtcct | 1161 |
rs192626 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895121 | gctgcagtgagccaa[A/G]atggcgccactgccc | 1161 |
rs290514 | snp | C/T | 0.41141 | 0.19091 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934494 | agaaaatcttcacaa[C/T]ctatacatccaacag | 1161 |
rs290515 | snp | C/T | 0.424968 | 0.178567 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934886 | tgtaagtatttggct[C/T]tacttgtgggttctc | 1161 |
rs290516 | snp | C/T | 0.425123 | 0.178415 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938502 | GGGATTACAGGCGTG[C/T]GCCACCACACCCGGC | 1161 |
rs290517 | snp | C/T | 0.232651 | 0.249397 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938602 | caggtgatccacctg[C/T]ctcggcctcccaaag | 1161 |
rs929780 | snp | C/G | 0.245631 | 0.249962 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893199 | AGGTGGTAGAATACT[C/G]TGATGTGATTCTGGA | 1161 |
rs952230 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900616 | TGACCATCAAACCTA[G/T]CCAACTGGAATAGTT | 1161 |
rs952231 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900401 | AAATGCCTGGCAATC[C/T]GACGTGCTCCTAATC | 1161 |
rs966497 | snp | A/G | 0.146314 | 0.227484 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915669 | ATTTCTTGGCTTGTG[A/G]TCCCCTTAATCCATC | 1161 |
rs976080 | snp | G/T | 0.23846 | 0.249734 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921824 | ATCAATTTTCATTAG[G/T]ATTTTATTTTTAAAA | 1161 |
rs976581 | snp | C/T | 0.424968 | 0.178567 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915598 | GTTGACAGGCTGCAT[C/T]CCTTTTTGGAGGCTC | 1161 |
rs976630 | snp | A/C | 0.491987 | 0.0627894 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919654 | ACCTTTATTATTTTT[A/C]TAGGTTAACTATATC | 1161 |
rs976631 | snp | C/T | 0.491987 | 0.0627894 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920216 | AGTCTGATTCTCCCA[C/T]CTTCCTGACAGTTAT | 1161 |
rs1021005 | snp | A/G | 0.491885 | 0.0631791 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895633 | TACATGTTTAAAAAT[A/G]TAACATTCCCTCATT | 1161 |
rs1038144 | snp | C/T | 0.238749 | 0.249747 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903374 | GTGAGTTGCATTAGT[C/T]TTTTTAATGTAGAAA | 1161 |
rs1047032 | snp | C/G | 0 | 0 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874334 | GTACCTCAGTTGTGA[C/G]CTTCAGCAGATTTTA | 1161 |
rs1048151 | snp | G/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932922 | AGGGCTTGCTTTTTG[G/T]CCTTACCCTTCTACC | 1161 |
rs1316649 | snp | A/G | 0.242775 | 0.249896 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936515 | gttgttgtcctttca[A/G]tttcatttatttctg | 1161 |
rs1382915 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900448 | TCATGTCCTCACAAG[A/G]ACCTCAACAATATTG | 1161 |
rs1382916 | snp | A/T | 0.21845 | 0.248001 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900538 | CTATTTTTTATTTAA[A/T]TTTTTTAAAAAAATA | 1161 |
rs1479646 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918676 | agccaactacactgg[A/T]cttctttcatcttga | 1161 |
rs1644458 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914785 | tttttttttttaaga[A/G]acaagagtcttgccc | 1161 |
rs1644460 | snp | C/T | | | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904806 | CCTGCTACCAAACAG[C/T]GCTTGGTGGAGACTG | 1161 |
rs1644462 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895101 | ctcactgcagcctcc[A/C]cctcccaggttcaag | 1161 |
rs1644463 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895080 | caggttcaagcaatt[C/T]tctctctcagcctcc | 1161 |
rs1644465 | snp | A/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891272 | GTGGTTTTTTACTAT[A/T]TGTATTTCCTCTTTT | 1161 |
rs1664211 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914787 | tttttttttttttaa[A/G]aaacaagagtcttgc | 1161 |
rs1812404 | snp | A/C/T | 0.183568 | 0.241012 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881851 | ggctcatgctcagtg[A/C/T]gctgcacccactgtc | 1161 |
rs1820082 | snp | C/T | 0.232651 | 0.249397 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936710 | tcccagaggttttga[C/T]aggttgtgtcactat | 1161 |
rs1820083 | snp | C/T | 0.424348 | 0.179172 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883006 | ACACACACACACACA[C/T]GTCTGTAGGTGGATA | 1161 |
rs2120954 | snp | G/T | 0.214239 | 0.247429 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923653 | tgtcttgtaaaaaaa[G/T]aagtatactaaagaa | 1161 |
rs2120955 | snp | C/T | 0.424968 | 0.178567 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923541 | ttttctctgaactta[C/T]catatacctcatcaa | 1161 |
rs2120956 | snp | C/T | 0.491885 | 0.0631791 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896279 | TGGAGTGCAATGGCG[C/T]GATCTCGGCTCACCG | 1161 |
rs2120957 | snp | C/T | 0.491834 | 0.0633738 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896442 | GTCTTGATCTCCTGA[C/T]CTCGTGATCCACCCA | 1161 |
rs2306350 | snp | C/T | 0.258843 | 0.249844 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890791 | AATGTGGATTAAAAG[C/T]ATAACTCCTCAGAAT | 1161 |
rs2306351 | snp | A/C | 0.257176 | 0.249897 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891148 | TAAAACACAACAAAG[A/C]CTAGGAGAAATACTT | 1161 |
rs2409837 | snp | A/T | 0.3748 | 0.216622 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908581 | tatatatatatatat[A/T]tatTTTTTTTTTAAA | 1161 |
rs2409838 | snp | A/T | 0.498277 | 0.0293024 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908583 | TATATATATATATAT[A/T]TTTTTTTTTTAAATA | 1161 |
rs2447805 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881960 | cattgctcacgctgg[A/G]agctgcagactggag | 1161 |
rs2590567 | snp | A/C | 0 | 0 | | | GRCh38.p7 | 5:60885634 | AAGCCACAATAAACC[A/C]AATTAGACGTGATAA | 1161 |
rs2590568 | snp | A/G | | | | | GRCh38.p7 | 5:60909869 | tgaggcaggagaatc[A/G]cttgaactcaggacg | 1161 |
rs2590570 | snp | C/T | 0.214239 | 0.247429 | | | GRCh38.p7 | 5:60925467 | GATATGTTTGAGTGG[C/T]CCATGGTAAGACCAG | 1161 |
rs2619904 | snp | C/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890874 | GAACATTTTAAATTC[C/G]TGTATCACTCTTACC | 1161 |
rs2619906 | snp | A/T | 0.244898 | 0.249948 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938350 | TAGCTACCTTTTTGA[A/T]TTTTTTTTTTTTTTT | 1161 |
rs2694518 | snp | A/G | 0.425277 | 0.178263 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938009 | AGTTAatatgtatgc[A/G]tgtgtgtgtgtgtgt | 1161 |
rs2694519 | snp | C/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938048 | ATACATACATACATA[C/T]ATATATATATATATA | 1161 |
rs2694520 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938044 | ATACATACATACATA[C/T]ATACATATATATATA | 1161 |
rs2711685 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881379 | agaaccactgctctc[C/T]tcaaagctgtcagac | 1161 |
rs3031040 | in-del | -/T/TTT | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908593 | ATATATTTTTTTTTT[-/T/TTT]AAATAATGGCTTTGT | 1161 |
rs3797559 | snp | C/T | 0.492037 | 0.0625946 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927914 | aagtcagaacagatt[C/T]gataaacttccactt | 1161 |
rs3797562 | snp | A/G | 0.25801 | 0.249872 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901273 | AGAAGTCATGGGTAA[A/G]AGGAAAAAAATCACA | 1161 |
rs3822578 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891469 | AAGAATGGTTGCATT[A/G]ATAAACCATTTGCCC | 1161 |
rs3832350 | in-del | -/A | 0.49389 | 0.0814969 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892140 | CACCCTAAAAAAAAA[-/A]CAGTAAGGTGGATGT | 1161 |
rs3925381 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882010 | ttggctccACctagt[G/T]ttttgtatttttagt | 1161 |
rs4235483 | snp | A/G | 0.428333 | 0.175206 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892395 | AAGTTCTTTGACATC[A/G]AGGATACCGAGCAAG | 1161 |
rs4235484 | snp | A/G | 0.23846 | 0.249734 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920806 | GCTACATAATATTCC[A/G]TGAGGAACTGTGATT | 1161 |
rs4339295 | snp | G/T | 0.425123 | 0.178415 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876913 | gtcaattttggcttt[G/T]gttgccattgctttt | 1161 |
rs4394077 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880967 | GTTTCCAGTTTTTCT[G/T]CTCTGTTTTTTCCCC | 1161 |
rs4395591 | snp | A/T | 0.338976 | 0.23363 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909972 | tctagaaaaaaaaaa[A/T]aataataataataaa | 1161 |
rs4464637 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880968 | TTTCCAGTTTTTCTG[C/T]TCTGTTTTTTCCCCA | 1161 |
rs4546327 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881475 | GAAGTCTACAGAGGC[C/T]GGCAGGCCTCCTTGA | 1161 |
rs4647025 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946721 | ggttactctactcat[C/T]tgtcaaaaacaataa | 1161 |
rs4647026 | in-del | -/GACGGCGGCTAC | 0.0115603 | 0.0751433 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946144 | CACAGAAGAGGTTAC[-/GACGGCGGCTAC]ACAGTGTGATTTCAA | 1161 |
rs4647027 | snp | A/T | 0.0329836 | 0.124112 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946083 | AACCCGCTCAACTAC[A/T]TGGCACGAATCCTAC | 1161 |
rs4647028 | snp | A/C | 0.240478 | 0.249819 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945999 | TGGAATGTCAACTCC[A/C]GAGAAAGGAATCAGC | 1161 |
rs4647029 | snp | G/T | 0.127254 | 0.217792 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945916 | GCGCATGGGGCCAGC[G/T]CCGGAGCCAGGGTGC | 1161 |
rs4647030 | snp | C/T | 0.127599 | 0.217986 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945740 | AGATTTCCGTGGACT[C/T]TTCCCTGCCTCCGTC | 1161 |
rs4647031 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945694 | AAACTGAGGCTCCTC[C/T]ACAGGCGTGGCTGGG | 1161 |
rs4647032 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945663 | AGGAAAGTGGTGGTG[C/T]GCCTTAACAGCGCAA | 1161 |
rs4647033 | snp | A/G | 0.0114282 | 0.0747228 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945637 | CGCAAGCAGCCCGGG[A/G]CACGCCGGGGGAAGG | 1161 |
rs4647034 | snp | A/G | 0.0329836 | 0.124112 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945623 | GGCACGCCGGGGGAA[A/G]GCGCTGGGTAGTAGG | 1161 |
rs4647035 | snp | C/T | 0.00899369 | 0.0664527 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945465 | CGCATGATGCGTTAG[C/T]TGACTAGGGGCTCTC | 1161 |
rs4647036 | snp | A/G | 0.127599 | 0.217986 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945165 | CACCGAGGCGGAGAA[A/G]TCAGGCCGGCCTCCA | 1161 |
rs4647037 | snp | C/G | 0.0244538 | 0.107838 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945141 | GCCTCCATCCTGGAG[C/G]CCTTCTAGTAACGGC | 1161 |
rs4647038 | snp | G/T | 0.0538199 | 0.154962 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945031 | GGCGACGTCCAGTGC[G/T]CCAGCCGGTGTGAGG | 1161 |
rs4647039 | snp | C/T | 0.00463729 | 0.0479285 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944916 | GTAAAGAAAACCTTA[C/T]TTTTTGGCTAACAGG | 1161 |
rs4647040 | snp | C/G | 0.0124219 | 0.0778244 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944854 | TTTGCCCCACACTTT[C/G]CCGTCTCATCGCTCT | 1161 |
rs4647041 | snp | A/G | 0.0110494 | 0.0735024 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944369 | GGTAACAGCTATTGC[A/G]TTTTGTTTTCTGCTT | 1161 |
rs4647043 | snp | C/T | 0.00344233 | 0.0413439 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944002 | TGTGAAGATATTTAC[C/T]TGGAGAACACAGTTG | 1161 |
rs4647044 | snp | C/T | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943973 | TGCTTATGAGTTCTG[C/T]GTTCTGGAGAAATTT | 1161 |
rs4647045 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940653 | GTGATTAGCTCAATT[G/T]TCAAAATCCTTTGTA | 1161 |
rs4647046 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940635 | AAAATCCTTTGTATA[C/T]GACTCAGGGTTAGAT | 1161 |
rs4647047 | snp | C/T | 0.0110494 | 0.0735024 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940294 | CTGCAGGCCACTATG[C/T]GTAGCCATAGCCATT | 1161 |
rs4647048 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940199 | TGTTTAGTTTTTATA[A/G]TAGTATTACCCAGAA | 1161 |
rs4647049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939957 | CTGAAGTCCAGACAA[A/G]ATTGATAAAAAAGAC | 1161 |
rs4647050 | snp | A/C | 0.00333889 | 0.0407222 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939846 | ATTCATAAAGGTAAA[A/C]CATCTCATCAGTAGT | 1161 |
rs4647051 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939762 | CAgcctgtaatccca[A/G]cactttgggaggcca | 1161 |
rs4647052 | snp | A/G | 0.491987 | 0.0627894 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939656 | ATCCAAAAATCAGCC[A/G]GGCGTGCTCCGGGTG | 1161 |
rs4647053 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939645 | agccgggcgtgctcc[A/G]ggtgcggtggcaggt | 1161 |
rs4647054 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939554 | tgaactgagactgtg[C/G]caccctccagcctgg | 1161 |
rs4647055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939493 | aactaaaagttatct[A/G]aaaataaaaaaaaaG | 1161 |
rs4647056 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939479 | GTTATCTAAAAATAA[-/A]AAAAAAGAAGTATTG | 1161 |
rs4647057 | in-del | -/GTTTTT | 0.0337553 | 0.125452 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930556 | tttgtttttgttttt[-/GTTTTT]agacggagtcttgct | 1161 |
rs4647058 | snp | G/T | 0.0111728 | 0.0739025 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929552 | tcacccaggctggag[G/T]gcaatgaagtgatta | 1161 |
rs4647059 | snp | G/T | 0.0111728 | 0.0739025 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929551 | cacccaggctggagt[G/T]caatgaagtgattat | 1161 |
rs4647060 | snp | C/T | 0.0111728 | 0.0739025 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929550 | acccaggctggagtg[C/T]aatgaagtgattatg | 1161 |
rs4647061 | snp | C/T | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929465 | TGCATAGGAGCCCAC[C/T]ACCATGCCCAGCTTA | 1161 |
rs4647062 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929348 | tcagcctcccaaagc[G/T]ctaggattacaggca | 1161 |
rs4647063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929289 | TTTTTATTTCTGTCC[A/G]TCTTTAAGAAACATT | 1161 |
rs4647064 | snp | A/G | 0.0522499 | 0.152954 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928715 | CATTATTAATTTCAA[A/G]TAAATACAAAACATC | 1161 |
rs4647065 | snp | C/T | 0.00345422 | 0.0414147 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928407 | tcgaattatcagttg[C/T]cttagctatacaatg | 1161 |
rs4647066 | snp | C/G | 0.236724 | 0.249647 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928029 | ATTAGGCCACATATA[C/G]CATTAACTAAAGGAA | 1161 |
rs4647067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927735 | AGCTGGGGGGGCACT[C/T]ACTTATGAAACATGC | 1161 |
rs4647068 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927706 | GCAGACATGAGCAGC[A/G]GGAGATAGCTGACTT | 1161 |
rs4647069 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927470 | CATAGAGAAAAGTCT[A/G]AAGACTCTTGCTACA | 1161 |
rs4647070 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927286 | ACTTGTTCAAAACAC[C/G]TGTTAATATTTACCA | 1161 |
rs4647071 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923530 | CTTACCATATACCTC[A/G]TCAACTATTGTTATT | 1161 |
rs4647072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923100 | ACTCCCAAAAGTAAG[G/T]CTTCCAGTGGTTTGG | 1161 |
rs4647073 | in-del | -/C | 0.399432 | 0.200425 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923095 | CAAAAGTAAGGCTTC[-/C]AGTGGTTTGGCTCCT | 1161 |
rs4647074 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921660 | CCTGATACTAATGGA[A/G]GAAAAAGGTTTAGAT | 1161 |
rs4647075 | snp | A/G | 0.04543 | 0.143705 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921612 | ATTCCCTCACCAAAC[A/G]CACACATACACATAT | 1161 |
rs4647076 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921600 | AACACACACATACAC[A/G]TATACCCACTCACCC | 1161 |
rs4647077 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921260 | ATTAGAATATATGCT[A/G]TGGAATATTTCGGAG | 1161 |
rs4647078 | snp | C/T | 0.25801 | 0.249872 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921211 | TTGGCTCTGGTGTTT[C/T]GCATTAGAAATACAA | 1161 |
rs4647079 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921001 | ACAAAACAAGATATC[A/G]CCTCAAATACTCTAG | 1161 |
rs4647080 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920997 | AACAAGATATCGCCT[C/T]AAATACTCTAGAACT | 1161 |
rs4647081 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920757 | GACATAAGTAAATGC[A/G]TAATGTGTCAGTCTT | 1161 |
rs4647082 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919797 | AAAAAGGTGATCATC[A/C]TCTTCCCCAAAGGGT | 1161 |
rs4647083 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919668 | TTTGTGGACTCAATG[A/C]TATAGTTAACCTATA | 1161 |
rs4647084 | snp | A/G | 0.00335007 | 0.0407899 | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919500 | ACTTTCCTTCTTTGT[A/G]TTCTCATTCCTTCAG | 1161 |
rs4647085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919249 | cccatccaccctcat[A/G]attatgttgaagcaa | 1161 |
rs4647086 | snp | G/T | 0.126909 | 0.217598 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918920 | ttcaaCATGTTATGT[G/T]TTTATggatggtggg | 1161 |
rs4647087 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918526 | TTTCTCGCCTTCTAC[A/C]CAGCTTGGACACAGG | 1161 |
rs4647088 | snp | C/T | 0.029987 | 0.118719 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918301 | ATCAAGCTCATTTGA[C/T]AAAACTCTGAAAGTA | 1161 |
rs4647089 | snp | C/T | 0.00107903 | 0.0232023 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918246 | AGTACATTAAAACAT[C/T]TGCAGATTGCTTTGT | 1161 |
rs4647090 | snp | C/T | 0.00332778 | 0.0406548 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917681 | ttaaatgtagtgtca[C/T]cccttcaaacttaac | 1161 |
rs4647091 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917610 | TCATAAAATCTTAGC[A/G]ATCCTTTCTTCAAAC | 1161 |
rs4647092 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917588 | TCTTCAAACTCTCTC[A/G]TACCTCTCTTTTCTA | 1161 |
rs4647093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916981 | TTCCTATTTCAATAC[A/G]TTCTCATACTACTTT | 1161 |
rs4647094 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916736 | AACAGTGTTGTGTAT[A/C]TAAATGTAAATTTAA | 1161 |
rs4647095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915962 | GGGCACCTAGAGGGG[A/G]ATACTCTAATAATGG | 1161 |
rs4647097 | snp | C/T | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905166 | GTAGATGCTGAGCCC[C/T]CTCCCCACCAGGGTG | 1161 |
rs4647098 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905029 | CAGGATTTCAAATTA[A/T]CAAGGTTTTTTGGGG | 1161 |
rs4647099 | snp | A/G | 0.0303129 | 0.119321 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904915 | TATTGCTTTGTTTTT[A/G]TACTTAAACCTTATA | 1161 |
rs4647100 | snp | C/T | 0.326889 | 0.237882 | synonymous-codon, intron-variant | ERCC8 | GRCh38.p7 | 5:60904838 | TGAGGAAACAGTTTA[C/T]AGTCATCATATGTCT | 1161 |
rs4647101 | in-del | -/T | 0.000115385 | 0.00759468 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904772 | GTAAGTGTATTCTTT[-/T]GTCTTTTGACATACT | 1161 |
rs4647102 | snp | A/G | 0.444932 | 0.15653 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903536 | AATGTACTTTGTGCT[A/G]GTTGTTGAGACTCAG | 1161 |
rs4647103 | in-del | -/ATAG | 0.0930568 | 0.194599 | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60903081 | AAGTTGATGAGATAG[-/ATAG]CATTTTTTGACATTA | 1161 |
rs4647104 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902686 | CATATGTTTGAAATA[C/T]CCCTGTAAACTTCAC | 1161 |
rs4647105 | snp | A/G | 1.64969e-05 | 0.00287196 | missense | ERCC8 | GRCh38.p7 | 5:60902460 | CTCCACGTTATGACT[A/G]TATCTTGGCAACAGC | 1161 |
rs4647106 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902020 | tagggacacagaggt[A/G]accaaggcTTTGAAA | 1161 |
rs4647107 | in-del | -/A | 0.0352966 | 0.128072 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901964 | GGCATATAGTCAAAA[-/A]TCAGTGATTACAGGG | 1161 |
rs4647108 | snp | A/G | 0.25912 | 0.249834 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901888 | ATATAGGAAAAGAAA[A/G]CAGGATCACTTAACT | 1161 |
rs4647109 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901692 | atcaaggatccagat[A/G]agggtggagggtaca | 1161 |
rs4647110 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901252 | AAAAATCACAAAAAG[C/G]CTTGTAGGAGGGATC | 1161 |
rs4647111 | in-del | -/TTA | 0.033042 | 0.124214 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901112 | GTAGAAGAAGAATTA[-/TTA]CGAAAGCTATTCATA | 1161 |
rs4647112 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900811 | AAGAAGCTTTCAATT[A/G]TAAGAATACTCCAGG | 1161 |
rs4647113 | snp | A/G | 0.237014 | 0.249662 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900605 | TTGGCTAGGTTTGAT[A/G]GTCATCTGTGAAAAG | 1161 |
rs4647114 | snp | G/T | 0.0114282 | 0.0747228 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900445 | TATTGTTGAGGTCCT[G/T]GTGAGGACATGATAG | 1161 |
rs4647115 | snp | C/G | 0.031825 | 0.122064 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900383 | TTGCCAGGCATTTTT[C/G]TTTAGAAATAATCTA | 1161 |
rs4647116 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900187 | CATTATTCACCTTAC[A/G]CTTACCGTTTTTTAT | 1161 |
rs4647117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900113 | AGCAAAGTGAAATTA[A/G]TTAATTGCTTGTCTT | 1161 |
rs4647118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899890 | GAGCTACTGTTGACT[A/G]TTGAATATTTGCTGA | 1161 |
rs4647119 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899818 | TACCTATATAACGAG[A/G]CCTCTGTGTGCCATA | 1161 |
rs4647120 | snp | G/T | 0.157609 | 0.238955 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899792 | CCATAAAATTAGAAA[G/T]GTGGGTGAGGGGTAC | 1161 |
rs4647121 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892460 | TAGACCACCACCACC[A/C]ACTCACACTCTGCCT | 1161 |
rs4647122 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892443 | CTCACACTCTGCCTG[C/T]CCATCTCAGTGCTGA | 1161 |
rs4647123 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892245 | GCCATTGAAGATAAA[A/G]CTACTGTATATAAGA | 1161 |
rs4647124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891505 | TAATATACACCCCCC[A/C]AAAAATATTATTCTT | 1161 |
rs4647125 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891341 | AAAATGATTCTTCAA[G/T]GTTGAAGTCTGTATT | 1161 |
rs4647126 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888454 | CCAAGTTATCTTGCG[C/G]ATTACCTGGCCTTCT | 1161 |
rs4647127 | snp | C/T | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887847 | GCTCAGTTATTTGGA[C/T]ACAGAAAGACAAACT | 1161 |
rs4647128 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887717 | GCTCTGACAAATCCT[A/G]ATACTATTTTTAAAT | 1161 |
rs4647129 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887584 | ATTTCAAAAATGATA[C/T]AATTCATTTCAGTTT | 1161 |
rs4647130 | snp | C/T | 0.00823815 | 0.0636491 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60887482 | CTGCAACATTCTGGC[C/T]TGGGTTCCATCCTTA | 1161 |
rs4647131 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887247 | TGGGCAATGTAGTGA[A/G]ACCCCATCTCAGAAC | 1161 |
rs4647132 | snp | A/G | 0.491885 | 0.0631791 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886893 | TTTACCTACTTGGAG[A/G]CATTTCTGTTGATTA | 1161 |
rs4647133 | snp | A/G/T | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886881 | GAGGCATTTCTGTTG[A/G/T]TTATTGTAAACATCA | 1161 |
rs4647134 | snp | A/C | 0.258288 | 0.249863 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886687 | TGAGATGGAGTCTCA[A/C]TCTGTCGCCCAGGCT | 1161 |
rs4647135 | snp | C/T | 0.258288 | 0.249863 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886651 | GCAGTGGCGTGATCT[C/T]GGCTCACTGCAACTT | 1161 |
rs4647136 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886571 | gggattacaggtacc[C/T]gccaccacgcctggc | 1161 |
rs4647137 | snp | A/G | 0.4983 | 0.0291038 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886497 | TCAGGCTGGTCTTCA[A/G]CTCCTGACCTCAAGT | 1161 |
rs4647138 | snp | C/T | 0.46885 | 0.12085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886395 | AAGACTTTGTTCTCA[C/T]GTCAAATTTTACCAG | 1161 |
rs4647139 | snp | C/G | 0.425277 | 0.178263 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876080 | ACAGTAAGAACACTT[C/G]GACACAGGAAGGGGA | 1161 |
rs4647140 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876053 | gggaacatcacacac[C/T]gggacctgttgtggg | 1161 |
rs4647141 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876029 | ttgtggggtgggggt[A/G]ggggggagggatagc | 1161 |
rs4647142 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875963 | acaccaacatggcac[A/G]tgtatacatatgtga | 1161 |
rs4647143 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875858 | atataaaaaattatc[A/C]aggcgtggtggcagg | 1161 |
rs4647144 | snp | A/G | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875711 | agattctgtctcaaa[A/G]ggaaaaaaaaaaTTT | 1161 |
rs4647145 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875603 | CTGAATAAAATTGTA[A/G]TAGTTGTAAAAGTTG | 1161 |
rs4647146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875420 | ATTTCTGTAGTTGCT[A/C]ATCACCTTGTTGTTT | 1161 |
rs4647147 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875150 | TATTCTCCATATTTG[A/G]TATTTGTTTATTTAT | 1161 |
rs4647148 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875015 | AGTGCCACTTTCTCC[A/G]GGTAATTCCAAAGAG | 1161 |
rs4647149 | snp | C/G | 0.0930568 | 0.194599 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875007 | TTTCTCCaggtaatt[C/G]caaagagttgttgag | 1161 |
rs4647150 | snp | A/G | 0.491834 | 0.0633738 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874778 | AATAATGTAATTGCT[A/G]TTTATCTGATATATT | 1161 |
rs4647151 | snp | A/G | 0.199994 | 0.244948 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874731 | AGCCTAAAATTATGA[A/G]GTAGAAAAAACAGAA | 1161 |
rs4647152 | snp | C/T | 0.0100143 | 0.070049 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874579 | TTGTCTCTGCTGAAA[C/T]TTTTTAAATGAGACT | 1161 |
rs4647153 | snp | C/T | 0.030278 | 0.119257 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874378 | CTGGGAAAGCCCTCA[C/T]TGCTACAGTACAAGT | 1161 |
rs4647154 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874319 | CCTTCAGCAGATTTT[A/G]TGAACTATAAGATGC | 1161 |
rs4647155 | snp | G/T | 0.159951 | 0.233219 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874176 | TCAAAAATAGTAGTT[G/T]AAATGGTAACATCAA | 1161 |
rs4647156 | snp | C/T | 0.0146672 | 0.084371 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874157 | TGGTAACATCAAAAT[C/T]ATTTTATTCTTTCTT | 1161 |
rs4647157 | snp | A/C | 0.0930568 | 0.194599 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874096 | ATTTAATTAACCATG[A/C]TTTATGTTAAACATT | 1161 |
rs4647158 | snp | C/T | 0.0130921 | 0.0798413 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874032 | GCATCACAGGAGGCT[C/T]TTAACTTTGTGAAAA | 1161 |
rs4647159 | snp | G/T | 0.0659589 | 0.169201 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873655 | GAGTTTCACTCTGTC[G/T]CTCAGGCCGGAGTGC | 1161 |
rs4647160 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873647 | ctctgtcgctcaggc[C/T]ggagtgcagtgtttt | 1161 |
rs4647161 | snp | C/T | 0.00438332 | 0.0466095 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873621 | gttttgatctcagct[C/T]actgcaaccttcacc | 1161 |
rs4647162 | snp | A/C | 0.483418 | 0.0895317 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873578 | gcaattctcctgcct[A/C]agcctcctgagtagc | 1161 |
rs4647163 | snp | G/T | 0.0111728 | 0.0739025 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873556 | ctgagtagctgggat[G/T]acaggctcccgccac | 1161 |
rs4647164 | snp | A/G | 0.0607341 | 0.163335 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873533 | CCCGCCACTGCGCCC[A/G]GTTAATTTTTTTGTA | 1161 |
rs4647165 | snp | A/G | 0.00755907 | 0.0610114 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873500 | ttcagtagagatggg[A/G]tttcaccatgttggc | 1161 |
rs4647166 | snp | A/G | 0.0337553 | 0.125452 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873472 | GGCCAGGCTGGTTGC[A/G]AACTGCTGACCTCAA | 1161 |
rs5868257 | in-del | -/A | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895189 | AAAAAAAAAAAAAAA[-/A]GGGATTCACTTTTTT | 1161 |
rs6449509 | snp | A/G | 0.216349 | 0.247725 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883474 | CTCACCAGGTTGTCA[A/G]TTCTACTGACAGATA | 1161 |
rs6449510 | snp | C/T | 0.25634 | 0.24992 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883491 | TCTACTGACAGATAG[C/T]GTCAATGTTATAGAA | 1161 |
rs6449511 | snp | C/G | 0.00913223 | 0.0669531 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889955 | CCCTTTTAGTTGCTG[C/G]GTTAAGGTGACGTCT | 1161 |
rs6449512 | snp | A/G | 0.498392 | 0.028309 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938415 | CTGGAGTGCAGTGAC[A/G]CTATGTCGGCTCACT | 1161 |
rs6869855 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898742 | TATTTTTATTGCTAA[A/C]CTAAAAATCATTCTA | 1161 |
rs6884966 | snp | C/T | 0.491885 | 0.0631791 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897512 | TATTAGCTATTATTA[C/T]TATCACCAAATTATA | 1161 |
rs6885974 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899950 | AGTAACCTTTCTTTT[C/T]CAGATAACAAGAACA | 1161 |
rs6889899 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940796 | ctgaacctaatcttg[C/T]taattaaatgttaaa | 1161 |
rs6894736 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934523 | cttccactctgtggg[C/T]tgtctgtttactctg | 1161 |
rs7445953 | snp | A/G | 0.259397 | 0.249823 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881162 | gctatcagctcagag[A/G]ctgcagaacagtgga | 1161 |
rs7446829 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911578 | ttcttttgctgtgca[A/G]aagctctttagttta | 1161 |
rs7701023 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890425 | AAAACAAACAAACAA[A/T]AGCCAGAGTATTTAA | 1161 |
rs7712816 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938052 | atacatacatacata[C/T]atatatatatatata | 1161 |
rs7726671 | snp | A/G | 0.234692 | 0.249531 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894767 | GTTTACTTCCTGATA[A/G]TAATTTTGATAAGCT | 1161 |
rs7728660 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933772 | actgtatcattctta[C/T]gcctttgtgtcctcc | 1161 |
rs7735913 | snp | C/G | 0.127254 | 0.217792 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878875 | ctatttccttcagtt[C/G]tgctctgaccttagt | 1161 |
rs9291698 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924267 | TTATATAAAGTGTTG[C/T]TATCTGCTaatatta | 1161 |
rs9686404 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880297 | tctggctgcccttaa[C/T]attttttccttcatt | 1161 |
rs9687099 | snp | A/C | 0.49168 | 0.063958 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879205 | tcttaatcctgagtt[A/C]tagtttgattgcact | 1161 |
rs9763418 | snp | C/T | 0.399432 | 0.200425 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880409 | gaatttgaatgttgg[C/T]ctgacttgctagatt | 1161 |
rs10040255 | snp | A/C | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931751 | ATATGATCATTTTTC[A/C]AATTACAACAGAATA | 1161 |
rs10044751 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912769 | gagatacattctatc[A/C]atacctagtttattg | 1161 |
rs10044801 | snp | A/C | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912959 | acttgatcatggtgg[A/C]taagctttttgatgt | 1161 |
rs10046059 | snp | C/G | 0.0930568 | 0.194599 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896926 | cctgtcacttctcca[C/G]tcacaagcctttagt | 1161 |
rs10055203 | snp | A/C | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944713 | CGGGGGAACCCCCCC[A/C]CCACCCCCGGGGAAC | 1161 |
rs10055204 | snp | A/C | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944714 | GGGGGAACCCCCCCC[A/C]CACCCCCGGGGAACC | 1161 |
rs10055249 | snp | A/C | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944735 | CCGGGGAACCCCCCC[A/C]ACCCCCGCCGCCCCC | 1161 |
rs10064187 | snp | G/T | 0.399253 | 0.200558 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914304 | ATATATTTAGGATAG[G/T]TAGCTCTTCTTGTTG | 1161 |
rs10064292 | snp | A/T | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931570 | caccttcacctccca[A/T]agtactgggattaca | 1161 |
rs10067156 | snp | A/C | 0.176861 | 0.239062 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897593 | AAGACTATAACCTAC[A/C]TAAAAACAAGTACTA | 1161 |
rs10071845 | snp | A/G | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892921 | TATGGATGTGGGTGC[A/G]CATTTCACCAAGGCA | 1161 |
rs10076937 | snp | A/G | 0.425123 | 0.178415 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907543 | tttttagtagagatg[A/G]ggtttcaccatattg | 1161 |
rs10550173 | in-del | -/AC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882971 | AATAGCCCTGGGAAA[-/AC]ACACACACACACACA | 1161 |
rs10661271 | in-del | -/T/TT | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875894 | TTTTTTCTTTTTTTT[-/T/TT]ATTATACTGTAAGTT | 1161 |
rs10691070 | in-del | -/A | 0.448708 | 0.151707 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898795 | CATTGAAAAAAAAAA[-/A]CAGGGAAAGGATGAC | 1161 |
rs10939874 | snp | A/T | 0.259397 | 0.249823 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880725 | ctccatcaggtcgtt[A/T]aaggacttgtctgca | 1161 |
rs11269163 | in-del | -/ATACATACATATATATATATAT | 0.340108 | 0.233197 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938041 | TACATACATACATAC[-/ATACATACATATATATATATAT]ATATATATATATATA | 1161 |
rs11323212 | in-del | -/T | 0.236724 | 0.249647 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885015 | CAGTCACATATTATC[-/T]TTTTTTTTTTCCTTT | 1161 |
rs11739125 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929554 | atcacttcattgcac[A/T]ccagcctgggtgaca | 1161 |
rs11741108 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911191 | cattaggtatttctc[A/C]taatgctatccctcc | 1161 |
rs11744082 | snp | C/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908963 | atctatatgtagact[C/T]taatatgacttttaa | 1161 |
rs11744109 | snp | C/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909037 | aggaaggtgaaggat[C/T]taaagctggagaatt | 1161 |
rs11744167 | snp | C/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909241 | caaaaatgccctatt[C/T]tgaaaaaaaaaaaaa | 1161 |
rs11744756 | snp | C/T | 0.242775 | 0.249896 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905888 | gtgggagtggttaga[C/T]gatgaatagatgctt | 1161 |
rs11748453 | snp | C/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888915 | ttgttccaatactgt[C/G]ctttatagcaaaagg | 1161 |
rs11950337 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904634 | atagtgtgtgtgtgt[A/G]tatatatatatatat | 1161 |
rs11951353 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936244 | tcctggtttaatcta[A/G]gagggttgcgtattt | 1161 |
rs11957440 | snp | A/C | 0.491732 | 0.0637633 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880507 | tcaggtacaccaatc[A/C]gatgtagatttggtc | 1161 |
rs12515955 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946038 | TTGAGCTCAATTTAA[A/G]AAACGTGGCAATAAT | 1161 |
rs12516552 | snp | C/G | 0.146314 | 0.227484 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881700 | tgctgtttgctaaga[C/G]cattggaaaagtgca | 1161 |
rs12520314 | snp | C/T | 0.110167 | 0.207236 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938339 | GGCCTGTAAGATAGC[C/T]ACCTTTTTGAATTTT | 1161 |
rs12522154 | snp | C/T | 0.399432 | 0.200425 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885673 | AGTATGCATATGGCA[C/T]TGGGTAGCTACTTAA | 1161 |
rs12654306 | snp | A/C | 0.510277 | 0.0822478 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889029 | TTTCTGACTTTGATA[A/C]TTTTGGATATACAGC | 1161 |
rs12655603 | snp | C/T | 0.491987 | 0.0627894 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908769 | gcagctgtggttgcc[C/T]accatttcaagataa | 1161 |
rs12656682 | snp | C/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60916000 | CTGGGTGTTTTCCTA[C/G]GCCCCCTTCTACTTA | 1161 |
rs12657309 | snp | A/G | 0.093417 | 0.194889 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910298 | ctagtataactttat[A/G]gcaagtcttgatatc | 1161 |
rs12696976 | snp | A/G | 0.258843 | 0.249844 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907079 | CAGTGTGACATCACC[A/G]TAAAAGATTATTCAT | 1161 |
rs13155076 | snp | A/C | 0.425123 | 0.178415 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885307 | ATGTGAGCCACCACA[A/C]CTGGCCACATATTAT | 1161 |
rs13177396 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940224 | taaacaaaatgcaga[G/T]acagctacttgagga | 1161 |
rs13185609 | snp | A/T | 0.273049 | 0.248935 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909975 | agaaaaaaaaaaaaa[A/T]aataataataaaaga | 1161 |
rs13188118 | snp | C/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931575 | tcacctcccaaagta[C/T]tgggattacaggtgt | 1161 |
rs13188864 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909278 | aaaaaaaaaaaaaaa[A/G]GCCACAAAGGActct | 1161 |
rs13353957 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914844 | AAAATGTTCGTATCT[A/G]TTGAGATGACtaata | 1161 |
rs13356565 | snp | A/G | 0.189576 | 0.242588 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881643 | cgaggctctgtgggc[A/G]tcggaccctccgagc | 1161 |
rs13356787 | snp | A/C | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907168 | TGCAGTATtcctcag[A/C]tatttcaaatcttct | 1161 |
rs13358851 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881624 | ctgctgtgctagcaa[C/T]gggcgaggctctgtg | 1161 |
rs13359074 | snp | C/T | 0.466618 | 0.124806 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906758 | aaataaataaataaa[C/T]aaacaaatacataca | 1161 |
rs17332991 | snp | A/C | 0.0825414 | 0.185628 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883533 | TGAGTTTAGAGGGGA[A/C]CTAGTTATGAGTTTA | 1161 |
rs28407266 | snp | A/G | 0.468949 | 0.12067 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923973 | TCATCACCTTAGAGT[A/G]TACACATGAATATTA | 1161 |
rs28449887 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926580 | CCTACTTAGTTATTT[A/T]AAAAAATATTCCACA | 1161 |
rs28479087 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904593 | TATCTGTTGAATATA[A/T]ATAGTACAATATCTG | 1161 |
rs28507971 | snp | C/T | 0.126564 | 0.217402 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896840 | TGAACAATTTATATA[C/T]ACATTCAGTACCATT | 1161 |
rs28882716 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914204 | GGTGTTAAAGTCTCC[C/T]ATTATTATTGTGTGG | 1161 |
rs28969397 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881271 | GGAGGCACCCCCCAG[C/T]AGGGGCAGACTGACA | 1161 |
rs33986769 | in-del | -/CA | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932691 | TTCACTGTAATAAAT[-/CA]CAGTCATGAGTAATT | 1161 |
rs34095595 | in-del | -/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897407 | GGATAGGACTTTTCC[-/C]ATGTTTTGCCAACTG | 1161 |
rs34115919 | in-del | -/CC | 0 | 0 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944706 | GAGCCCGCGGGGGAA[-/CC]CCCCCCCCACCCCCG | 1161 |
rs34192517 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881263 | CTGTGAGGTGTCAGT[C/G]TGCCCCTACTGGGGG | 1161 |
rs34253881 | in-del | -/A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923096 | GGAGCCAAACCACTG[-/A/G]AAGCCTTACTTTTGG | 1161 |
rs34284817 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889214 | TCCTTCAGGGTAAAA[-/A]TTAATCTTTTTAGTT | 1161 |
rs34324683 | in-del | -/TA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886066 | ATATGTATATATATA[-/TA]CAAACATTGTTTTTA | 1161 |
rs34389481 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885883 | GACATAGTCCTTTTT[-/T]CATAAAGGAACTAAA | 1161 |
rs34477732 | in-del | -/T/TTT/TTTT | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907355 | TTTTTTTTTTTTTTT[-/T/TTT/TTTT]GAGATGGAGTCGCTC | 1161 |
rs34500722 | multinucleotide-polymorphism | GC/TT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60880967 | GTTTCCAGTTTTTCT[GC/TT]TCTGTTTTTTCCCCA | 1161 |
rs34555262 | in-del | -/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936831 | AGGTGTGTGATCCTT[-/C]TGGGGGTGTTAAACA | 1161 |
rs34599634 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943616 | ACAGATTAAAAGAGG[-/A]AAATTGGCCAAAAGA | 1161 |
rs34639423 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893739 | ACTCCGCCCACTGGG[-/G]CAGTCTCCACGAGGG | 1161 |
rs34676209 | snp | G/T | 0.240478 | 0.249819 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941869 | TGGTTAAATATAATG[G/T]CTACTTTTTTCCTTA | 1161 |
rs35012416 | in-del | -/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917545 | AGTGATTTTAGTAGT[-/G]CCAGATGTGCAGTAA | 1161 |
rs35095239 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939407 | TTGGGTAAAATATTT[-/G]CTATGAACCTTAGCA | 1161 |
rs35162023 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897674 | GTAGTATTAAATAAA[-/A]GTACTACATATTCTG | 1161 |
rs35254362 | in-del | -/T | 0.318896 | 0.240319 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893985 | TCCTGGGAATTTATC[-/T]TTTTTTTTTTTTTTT | 1161 |
rs35263498 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886008 | TAAGATTACCTTAAG[-/G]TGTTTCCAACTACAT | 1161 |
rs35285482 | in-del | -/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877502 | TGATTCTTCCTACCC[-/C]ATGAGCATGGAATGT | 1161 |
rs35290874 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929265 | ACAGGATTAAAAAAA[-/A]TTCCTTGAAATGTTT | 1161 |
rs35319315 | snp | G/T | 0.26271 | 0.249677 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912978 | GCTTTTTGATGTGCT[G/T]TTGGATTCAGTCTGC | 1161 |
rs35366433 | snp | C/T | 0.00365001 | 0.0425639 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60903694 | CAAGTCACAAAGTTG[C/T]ACTTTGGGTCCTCTA | 1161 |
rs35383830 | snp | A/G | 0.21875 | 0.248039 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915109 | TAAAAAAAGTTTACA[A/G]AAGTTCCTTTTTTTC | 1161 |
rs35410892 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899283 | ACAATGGCCACAAAA[-/A]TGTTACTATTTCTGT | 1161 |
rs35416057 | in-del | -/G | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908697 | AAGAAGCAGAGAAAA[-/G]TCATGACATTATAAA | 1161 |
rs35429862 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927446 | CGTGCAATAAAGCGG[-/G]AAAATCACTGTAGCA | 1161 |
rs35456838 | in-del | -/GTGTGT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904622 | TGTTGAATATATATA[-/GTGTGT]GTGTGTGTATATATA | 1161 |
rs35483171 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908225 | AGTTCAGATTTTTTT[-/T]TTTTTTGGTTTGGAA | 1161 |
rs35486204 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60928538 | ACCATTAGACTTTTT[-/T]GAGAGTAGCAACTAT | 1161 |
rs35546392 | snp | G/T | 0.399432 | 0.200425 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879907 | ATTTGATCCTGTCAT[G/T]ATGACATTAGCTGGT | 1161 |
rs35547744 | in-del | -/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936271 | TTTCCAGGAATTTAT[-/C]TCATCTCCTCTAAGT | 1161 |
rs35617853 | snp | C/T | 0.238749 | 0.249747 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880721 | TCAGCTCCATCAGGT[C/T]GTTAAAGGACTTGTC | 1161 |
rs35653226 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923581 | TGGAGGATATTCTTG[-/G]AAATGTGCAAATATT | 1161 |
rs35713268 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906423 | GAGTTTTGGAGAAGG[-/G]CTATTATCATTTAAA | 1161 |
rs35742543 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920829 | ATGTAGCACGTAGAA[-/A]TAGGTGAAAATACTA | 1161 |
rs35775565 | in-del | -/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934454 | CTTGATTTGAGTTCC[-/C]TTGAATATTCTGGAT | 1161 |
rs35789098 | in-del | -/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891674 | TTCTTTTTTTTTTTT[-/T]CCTGCTGATACTTCT | 1161 |
rs35852200 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885920 | TATGAAAAATGTTTT[-/A]TTGAATGTCAAACGT | 1161 |
rs35948426 | snp | A/G | 0.425277 | 0.178263 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889598 | GAGCCACTGTGCGCA[A/G]CCATTGTCACGATTT | 1161 |
rs35957723 | snp | A/G | 0.146314 | 0.227484 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932792 | TCCCCCAACACAATG[A/G]CATAGGAGTAGAGGG | 1161 |
rs36065070 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898824 | GGAAAGGATGACTGT[-/T]GTAGTCTCAAAATTT | 1161 |
rs36091580 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907337 | CTTCTTCACTCCTGT[-/T]ATCATAGAAACATGA | 1161 |
rs36122974 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930363 | AAGATTGAGACCATT[-/T]CTGGCCAACATGGTG | 1161 |
rs41544812 | snp | C/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918722 | CCAAAACCAAAACAG[C/T]TGTCTCTTCCAGTAA | 1161 |
rs41556112 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898019 | GAGTGCAAAGCGTAG[C/T]AGAGAAAAATAAAAG | 1161 |
rs41562418 | snp | A/T | 0.000451488 | 0.015018 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874715 | GTAGAAAAAACAGAA[A/T]CTTCCTTTTTCTTTA | 1161 |
rs55638584 | in-del | -/A/AA | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914790 | AAAAAAAAAAAAAAA[-/A/AA]GGATATTGACTTTTA | 1161 |
rs55700838 | snp | C/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918701 | TCTTGAAAGAGTGAT[C/T]TGGTCTTACTGGAAG | 1161 |
rs55704074 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898202 | TAAATGAGTTAAATA[C/T]ATAAAAAAATCAAGT | 1161 |
rs55758463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897981 | TAGCTTCATATCTTT[A/C]ATTTATATCAGTAGT | 1161 |
rs55807411 | in-del | -/T | | | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60873923 | ATTAATGAGGCAGGA[-/T]TTGGTCATACCTTAA | 1161 |
rs55859038 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897887 | TCATGCTAGCACTCA[A/G]AAAGTTTCAGATTTT | 1161 |
rs55905414 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899531 | ATCATAAAGTTTGCA[-/A]TTTGTCAATATGCGT | 1161 |
rs55910841 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904683 | ATATATATATATATA[A/T]AAAATTGTGATATTC | 1161 |
rs56015997 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60921964 | TCGCTTGACCCATTC[-/T]ACTTGACTGCAATTT | 1161 |
rs56108456 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60921972 | ACCCATTCACTTGAC[G/T]GCAATTTTCATGTTT | 1161 |
rs56176128 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934162 | TAAGGAATCTCCACA[C/T]TGTTTTCCATAGTGG | 1161 |
rs56186848 | in-del | -/A | | | frameshift-variant | ERCC8 | GRCh38.p7 | 5:60891009 | ATATGGTACAAAAAC[-/A]AATTCTGAACTGCAG | 1161 |
rs56256328 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899933 | AAATAGCAAAAAAAA[A/C]AAGTAACCTTTCTTT | 1161 |
rs56263748 | snp | A/C | 0.00022194 | 0.0105319 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898252 | CTTAATTTATACCCA[A/C]ATATATACTTAAAAA | 1161 |
rs56376749 | snp | C/T | 0.000313865 | 0.0125233 | synonymous-codon, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922092 | ACATGTGTAATAAGA[C/T]TGTCTGCTGGAGTTC | 1161 |
rs56702003 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876819 | CAAAAATTTTCTCCC[A/T]TTCTGTAGGTTGCTT | 1161 |
rs56791802 | snp | A/G | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935910 | ATCATGGTGGATTAT[A/G]TTTTTTATATGCTGC | 1161 |
rs56831295 | in-del | -/GTGTGTAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904630 | ATATATAGTGTGTGT[-/GTGTGTAT]ATATATATATATATA | 1161 |
rs58372638 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929737 | CATCATTATCCTGGT[A/G]AGCATATTATTAAGA | 1161 |
rs58853350 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914810 | AAAAAAAAAAAAAAA[C/G]GATATTGACTTTTAT | 1161 |
rs59797139 | in-del | -/CACACA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883005 | ACACACACACACACA[-/CACACA]TGTCTGTAGGTGGAT | 1161 |
rs60064294 | in-del | -/AAAAAAA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909272 | AAAAAAAAAAAAAAA[-/AAAAAAA]GCCACAAAGGACTCT | 1161 |
rs60858663 | snp | C/T | 0.491936 | 0.0629843 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911304 | CTAACTGGTGTGAGA[C/T]GGTATCACACTGTGG | 1161 |
rs60986431 | snp | A/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919072 | AACAAACTGGCTTTT[A/T]AGAGAGATTTATGAG | 1161 |
rs61101592 | snp | C/T | 0.491885 | 0.0631791 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884424 | GAGCTTGCAGTGAAC[C/T]GAGATTGTGCCACTG | 1161 |
rs61605031 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892519 | CAGCTAGGACAGTTT[G/T]GGCTGCCTGCTCCTG | 1161 |
rs61613461 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911439 | CTACTTTTTGATGGG[G/T]TTTTTTTTTTCTTGT | 1161 |
rs61754098 | snp | G/T | 0.00380205 | 0.0434346 | missense | ERCC8 | GRCh38.p7 | 5:60898280 | AAATCTCTTACAAGT[G/T]TGTTTTCTCCATTGG | 1161 |
rs61759478 | snp | C/T | 6.6011e-05 | 0.00574466 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928886 | CTTCAACAGGTTCAA[C/T]GTCAAGGGTGTTAAT | 1161 |
rs62372110 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60880910 | TGTTGCTGGTGAGGA[A/G]CTGCGTTCCTTTGGA | 1161 |
rs62372133 | snp | G/T | 0.491885 | 0.0631791 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906350 | ATGTTTTAGCAGAAT[G/T]CAGGCTTGTCTCCTC | 1161 |
rs62372134 | snp | A/T | 0.491885 | 0.0631791 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906420 | GTTGAGTTTTGGAGA[A/T]GGGCTATTATCATTT | 1161 |
rs62372135 | snp | C/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906754 | AAATAAATAAATAAA[C/T]AAATAAACAAATACA | 1161 |
rs62372136 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907186 | TTTCAAATCTTCTCC[A/G]CAAATATACCAACTC | 1161 |
rs62372137 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909609 | TATATTTCTCTTCCT[A/C]ATGATTTTCTTAATA | 1161 |
rs62372139 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930926 | AGCCTGGCCAACATG[A/G]TGAAACCCCGTCTCT | 1161 |
rs62372142 | snp | G/T | 0.145978 | 0.227331 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939005 | GAGAAACAGCTTTTA[G/T]CTTTATTTGTTTTAA | 1161 |
rs70977811 | in-del | -/GTGTATATATAT | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904632 | ATATAGTGTGTGTGT[-/GTGTATATATAT]ATATATATATATATA | 1161 |
rs70977813 | in-del | -/AACAAA | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930577 | AAAAACAAAAACAAA[-/AACAAA]CTAAAAAATGAGCCA | 1161 |
rs70977814 | in-del | -/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933236 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC | 1161 |
rs70977815 | in-del | -/C/CA/CACA/CACACA | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933957 | ACACACACACACACA[-/C/CA/CACA/CACACA]ACCACATTTTCTTTA | 1161 |
rs70977816 | in-del | -/C | 0 | 0 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944735 | CGGGGAACCCCCCCC[-/C]ACCCCCGCCGCCCCC | 1161 |
rs71578645 | in-del | A/TTTT | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939487 | GCAATACTTCTTTTT[A/TTTT]ATTTTTAGATAACTT | 1161 |
rs71606647 | in-del | -/A | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884494 | GCCAGACTCCTTCTC[-/A]AAAAAAAAAAAAAAA | 1161 |
rs71606648 | in-del | -/TTT | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884523 | ATATGTGTGTATGTG[-/TTT]TTTTTTTTTTTTTTG | 1161 |
rs71606652 | in-del | -/AC/ACAC/ACACAC/ACACACAC | 0.28194 | 0.274775 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933938 | GTAGTATTCCATGAT[-/AC/ACAC/ACACAC/ACACACAC]ACACACACACACACA | 1161 |
rs71630085 | snp | G/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925820 | ACTGCATTGACATTG[G/T]CATCTTTCTTTCTTT | 1161 |
rs73112244 | snp | C/T | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884786 | CATACCATTTTATAT[C/T]AATATGAGAATGACT | 1161 |
rs73112254 | snp | A/G | 0.095934 | 0.196885 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893760 | TCCACGAGGGGGCGG[A/G]GCTTCTCCCTTCCCT | 1161 |
rs73112261 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908359 | AAATCTGTATATTCA[C/G]TGTAGACCTCACTCC | 1161 |
rs73114340 | snp | A/T | 0.093417 | 0.194889 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942908 | GGAAGAACAGTAGAC[A/T]TCTCCTATGAATAAA | 1161 |
rs73759435 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885861 | ATTATATTTTCATGT[A/G]GTTTTTGACATAGTC | 1161 |
rs73759436 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889069 | GTAGACTGCCCTTCA[C/T]ATTTGGCTTGTCTTA | 1161 |
rs73759437 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899178 | TATCAAAATTTCTAC[A/G]CAGGAATTAAATTCT | 1161 |
rs73759439 | snp | G/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904622 | TGTTGAATATATATA[G/T]TGTGTGTGTGTGTAT | 1161 |
rs73759440 | snp | A/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904623 | GTTGAATATATATAG[A/T]GTGTGTGTGTGTATA | 1161 |
rs73759441 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907303 | CTACAAACACATTTG[C/T]TTCCACTTATCCTTT | 1161 |
rs73759442 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926384 | ATGTTTTAGCACAAG[A/T]TCCTTATCTTGTGAC | 1161 |
rs73759445 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938909 | TGTTTACAGTTGTCT[A/G]ATCTCTCTTTATCCT | 1161 |
rs73759446 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939076 | AGCCTGTTCACCTTT[C/G]TTATGACATCTGATA | 1161 |
rs74316631 | snp | C/T | 0.132751 | 0.2208 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884647 | TAAATTATAAACATA[C/T]ATGTAAGGAATAGGA | 1161 |
rs74365156 | snp | G/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881048 | TGGGTTTTTGGTGTG[G/T]ATGTCCTTTCTGTTT | 1161 |
rs74405304 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918142 | GTCTAGCTCTTCTTA[A/C]CCACTGTACTGCTTT | 1161 |
rs74420406 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888402 | GCTGATGCAAAGATA[C/T]ATATGTTCAGTGCCC | 1161 |
rs74635817 | snp | A/C | 0.444444 | 0.157135 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881265 | ACCCCCCAGTAGGGG[A/C]AGACTGACACCTCAC | 1161 |
rs74692291 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | ERCC8 | GRCh38.p7 | 5:60943107 | GAGACCCCATCTCTA[C/T]GAAAAATTTAAAAAT | 1161 |
rs74699705 | snp | A/G | 0.375 | 0.216506 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881279 | ACCCCCTACTGAGAG[A/G]TGCCTCCCAGGTAGG | 1161 |
rs74786103 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942443 | AACTGTGGTATATCT[A/G]CACAGTGGGATACTC | 1161 |
rs74811299 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914601 | TTGACACCAGCCTGG[G/T]CAAGACAGAGAGACA | 1161 |
rs74916680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894378 | GGTAATAACTGAGAA[C/T]AGGTATATATTCCTA | 1161 |
rs74938928 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897511 | ATATTAGCTATTATT[A/G]TTATCACCAAATTAT | 1161 |
rs74954831 | snp | C/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892498 | TGATCTTCCCGCTCA[C/T]CCAGTCAGCTAGGAC | 1161 |
rs74992137 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933642 | ACATAAGTTCTTCAG[G/T]GGTGATTTCTGAGAT | 1161 |
rs75006130 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895892 | GTGTTGAATGAGGTA[C/T]GAATATTGAACCAGG | 1161 |
rs75040088 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896630 | TTTCTGGTATCAACC[A/G]TAAGTATTCTATGTA | 1161 |
rs75105968 | snp | A/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882958 | GATAACTACCAAAAA[A/T]AGCCCTGGGAAAACA | 1161 |
rs75120379 | snp | A/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882971 | AATAGCCCTGGGAAA[A/G]CACACACACACACAC | 1161 |
rs75274920 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932331 | TGGGATTTCAGGAGG[G/T]TGCCCACCATGACTG | 1161 |
rs75295262 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908945 | TTGTTAACAGAAAGG[C/T]GTATCTATATGTAGA | 1161 |
rs75313393 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875949 | AACGTGCAGGTTTGT[C/T]ACATATGTATACATG | 1161 |
rs75418851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885131 | ATCCTCCCACCTCAC[C/T]CTCTTAAGTAGCTGG | 1161 |
rs75465660 | snp | A/C | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915002 | AATAGTTGATTTAGG[A/C]TTTTTGTTATTTATA | 1161 |
rs75544693 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881307 | TGGGGGTCAGGGGTC[A/G]GGGACCCACTTGAGG | 1161 |
rs75627604 | snp | C/T | 0.375 | 0.216506 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881491 | TGGAGCCCACCACAG[C/T]TCAAGGAGGCTGGCC | 1161 |
rs75787078 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909196 | CATCGAGGACAAAGG[A/G]TATCTGCCTGAACAA | 1161 |
rs75792078 | snp | A/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881268 | GGCACCCCCCAGTAG[A/G]GGCAGACTGACACCT | 1161 |
rs75810155 | snp | A/C | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882972 | ATAGCCCTGGGAAAA[A/C]ACACACACACACACA | 1161 |
rs75919961 | snp | C/T | 0.277778 | 0.248452 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881150 | AGCCTCTGCTGCTGA[C/T]ACCCAGGCAAACAGA | 1161 |
rs75941815 | snp | A/C/T | 0.0154624 | 0.086631 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897083 | CTTAGCTCTTCCTTG[A/C/T]GTATCCCAAGGAAGT | 1161 |
rs75979228 | snp | A/C | 0.0988009 | 0.199095 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932189 | GAAAAGGGCAATAAT[A/C]CTATAAAGGGAAAGA | 1161 |
rs76006578 | snp | G/T | 0.32 | 0.24 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881524 | CAGTTCGAGCTTCCC[G/T]GCTGCTTTGTTTACC | 1161 |
rs76058802 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932902 | GGGAAGGCAGAAGAG[C/G]CTGGGGTAGAAGGGT | 1161 |
rs76068959 | snp | A/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881311 | GGGTCGGTGTCAGGG[A/T]CCCACTTGAGGAGGC | 1161 |
rs76090939 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921085 | TCAACACGCTTTTAA[A/G]AAGATAGTATTTCAT | 1161 |
rs76133722 | snp | C/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881131 | GGCAAACAGGGTCTG[C/G]AGTGGACCTCCAACA | 1161 |
rs76157730 | snp | A/G/T | 1.64939e-05 | 0.0028717 | missense | ERCC8 | GRCh38.p7 | 5:60902470 | AGATATAGTCATAAC[A/G/T]TGGAGACCAGGAAAC | 1161 |
rs76202054 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931977 | CAGCTTGGGCTCTGA[C/T]TTCTGTCTCCTCTAA | 1161 |
rs76459813 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897527 | TTATCACCAAATTAT[A/G]AGCTTTTAGTAGTTT | 1161 |
rs76551326 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881277 | TAACTGGGAGGCACC[A/C/T]CCAGTGGGGGGAGAC | 1161 |
rs76588026 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942299 | GTAGCTCCACTGTTA[C/T]GCATTAACTTCAGAG | 1161 |
rs76592390 | snp | A/C | | | missense | ERCC8 | GRCh38.p7 | 5:60891008 | CATATGGTACAAAAA[A/C]AAATTCTGAACTGCA | 1161 |
rs76614815 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928525 | TTATATTTATTTTAC[C/T]ATTAGACTTTTTTGA | 1161 |
rs76810802 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923919 | ATTATCATGATTTTT[A/G]TCGTAGTCACTGTCT | 1161 |
rs76836572 | snp | A/C | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884475 | AGCCAGACTCCTTCT[A/C]AAAAAAAAAAAAAAA | 1161 |
rs76853557 | snp | A/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881123 | GGGTCTGGAGTGGAC[A/G]TGTAGCAAACTCCAA | 1161 |
rs76858571 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922592 | TCAACATTTGTAAAG[A/G]AGGGGGACATTTTTA | 1161 |
rs76866604 | snp | A/G | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916507 | ATCTAGCTTTTCTCA[A/G]TGGAGGTGCTGGTTT | 1161 |
rs76867053 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932627 | CCTGGTTTCCTCCAC[A/G]CTTTGCCCATGCACC | 1161 |
rs76910838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922843 | AACAAGTAGTATGCA[C/T]AATCACACAAATTAT | 1161 |
rs76994019 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940606 | GAACTCATCCCTGAG[C/T]GAGGCATGCATAGAT | 1161 |
rs77068501 | snp | C/T | 0.093417 | 0.194889 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906912 | CCTACTGCCACAGTT[C/T]TCTCACTGATATAAG | 1161 |
rs77082648 | snp | A/G | 0.0327778 | 0.123752 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905877 | TGGGGGAAGGGGTGG[A/G]AGTGGTTAGATGATG | 1161 |
rs77149936 | snp | C/G | 0.0538451 | 0.154994 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945414 | GGCAGCGATTGCGTG[C/G]TCAGTGATTGCGAGG | 1161 |
rs77194122 | snp | A/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881479 | CAGCTCAAGGAGGAC[A/T]GCCTGCCTCTGTAGG | 1161 |
rs77230476 | snp | C/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881158 | CTGGTCTGCAGCCTC[C/T]GCTGCTGATACCCAG | 1161 |
rs77239489 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943883 | ACACTGGCAAAAAAA[A/C]CACATTAAAGGAACT | 1161 |
rs77334886 | snp | A/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909962 | CGAGACTCCGTCTAG[A/G]AAAAAAAAAAAATAA | 1161 |
rs77413246 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914713 | GAATCCCTTGAGCCC[A/G]GAGTTTGAGGTTATA | 1161 |
rs77502795 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891394 | AAAAACGTAAGACAT[A/T]AGTGATACAAGTGAG | 1161 |
rs77518885 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924932 | CTCTCATTTATTATA[C/T]GTTTATAAAACAACT | 1161 |
rs77551122 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882348 | TGTTAAACAGATTAC[A/T]TTATTAAACTTAATG | 1161 |
rs77558088 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881264 | CCCCCCAGTAGGGGC[A/G]GACTGACACCTCACA | 1161 |
rs77651580 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881510 | CGGTGGGCTCCACCC[A/T]GTTCGAGCTTCCCAG | 1161 |
rs77717353 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909961 | GCGAGACTCCGTCTA[A/G]AAAAAAAAAAAAATA | 1161 |
rs77768961 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888701 | AATAATCTCAAAATG[A/T]AAGTTACAAGTGCAG | 1161 |
rs77910376 | in-del | -/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876009 | CATTAGGTATATCTC[-/C]TAATGCTATCCCTCC | 1161 |
rs78116676 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904439 | AATTTCCTTGTTTTA[G/T]TGTGTCAAATTGGGA | 1161 |
rs78131263 | snp | C/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881396 | CAGACTTAAATGTCC[C/T]TGTCTGACAGCTTTG | 1161 |
rs78162412 | snp | A/G | 0.110167 | 0.207236 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942831 | TAAAATGTTTTTTTA[A/G]AGGGTGTAAACTGTG | 1161 |
rs78167706 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881558 | GGGAGGGGCATCCAC[C/T]ATTGCTGAGGCTTGA | 1161 |
rs78232441 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ERCC8 | GRCh38.p7 | 5:60943006 | GGCTGTGTGGTAGCT[C/T]GCACATATAATCCCG | 1161 |
rs78241666 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881286 | AGAGTAGCAAAACTG[A/G]GAGGCACCCCCCAGT | 1161 |
rs78267143 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919631 | ACTAATTTTCTCTTT[C/G]CTCTCTTACCTTTAT | 1161 |
rs78282968 | in-del | -/TTT | 0.24019 | 0.249807 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939479 | CGGTTGCAATACTTC[-/TTT]TTTTTAATTTTTAGA | 1161 |
rs78317809 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895387 | ATGGCAGTAGCAGTA[C/T]AGTGGGTTAAATATT | 1161 |
rs78387646 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897469 | AATTATTATTAGCAC[A/G]GTATCTGACATACAA | 1161 |
rs78436347 | snp | C/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882965 | ACCAAAAATAGCCCT[C/G]GGAAAACACACACAC | 1161 |
rs78455238 | snp | A/C | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882961 | AACTACCAAAAATAG[A/C]CCTGGGAAAACACAC | 1161 |
rs78528578 | snp | A/C | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904162 | AGTTTTTCCAAGTTA[A/C]TGATATACTTCCAAT | 1161 |
rs78572934 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883668 | TATACATTGACACAA[C/G]TGATATGTAAAACAG | 1161 |
rs78581134 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914605 | CACCAGCCTGGGCAA[A/G]ACAGAGAGACACTGC | 1161 |
rs78588277 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920089 | TTATTCAAAGCTGAG[A/G]AGTTGAGAGTCTGCG | 1161 |
rs78618185 | snp | A/T | 0.000148472 | 0.00861475 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60902507 | TATTTCTTGTCTGTG[A/T]CCTGCAAATACAACT | 1161 |
rs78753279 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881050 | ACAAACAGAAAGGAC[A/G]TCCACACCAAAACCC | 1161 |
rs78817947 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883023 | TCTGTAGGTGGATAA[A/G]CCACATGAGGGCCAT | 1161 |
rs78847284 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881310 | TGCTTGGGGGTCAGG[C/G/T]ACCCACTTGAGGAGG | 1161 |
rs78877653 | snp | C/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881309 | CTCCTCAAGTGGGTC[C/T]CTGACCCCTGACCCC | 1161 |
rs78976873 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910938 | TAATGCAAAGGGAAA[C/G]CTTTCAACATTTTAC | 1161 |
rs78979652 | snp | C/G | 0.21875 | 0.248039 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934091 | actactgggtatcta[C/G]ctagtggaaaagaag | 1161 |
rs79004097 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881119 | CTGGAGTGGACCTCC[A/G]GCAAACTCCAACAGA | 1161 |
rs79024544 | snp | A/C | 0.444444 | 0.157135 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881481 | CACAGCTCAAGGAGG[A/C]CTGCCTGCCTCTGTA | 1161 |
rs79064804 | snp | A/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941157 | CTCATCTCTAAAAAT[A/T]AAAAAAAAGCTTGAG | 1161 |
rs79166217 | snp | C/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881134 | TGGAGGTCCACTCCA[C/G]ACCCTGTTTGCCTGG | 1161 |
rs79166643 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905950 | GGTGTGGGGAATGGT[C/G]CTCTTGTGCACTAAG | 1161 |
rs79206648 | snp | A/C | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881142 | CTGCTGATACCCAGG[A/C]AAACAGGGTCTGGAG | 1161 |
rs79222208 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919977 | CAAACTCCTATTTAG[A/G]GGAAATGCCCTTTGT | 1161 |
rs79306787 | snp | C/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881138 | ATACCCAGGCAAAGA[C/G]GGTCTGGACTGGACC | 1161 |
rs79314404 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922398 | TACTTCCATAACTTC[A/C]AAAAGAAAGGGTGAC | 1161 |
rs79422128 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919229 | AACGATAGGTTGTTC[A/G]AGATTTGCTTCAACA | 1161 |
rs79598443 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881156 | TGCCTGGGTATCAGC[A/G]GCAGACACTGCAGAA | 1161 |
rs79845929 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914595 | CAGATTTTGACACCA[A/G]CCTGGGCAAGACAGA | 1161 |
rs79897465 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932789 | ACTTCCCCCAACACA[A/G]TGGCATAGGAGTAGA | 1161 |
rs79940900 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908040 | CCTGATTTTCCTCTT[G/T]CTCTCCTTGGCTACA | 1161 |
rs80039161 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945924 | GCTCCGGCGCTGGCC[C/G]CATGCGCCTTCCTTA | 1161 |
rs80168913 | snp | C/T | 0.234692 | 0.249531 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878948 | CTTCTCTAGTTCTTT[C/T]AATTGTGATGTTAGG | 1161 |
rs80243625 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934161 | TTAAGGAAATTCCAC[A/G]CTATTTTCCATAGTG | 1161 |
rs80243820 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882309 | AGAGCTGGAAAACAA[A/T]ATATTAATTTAGGCA | 1161 |
rs80285184 | snp | C/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881047 | AACAGAAAGGACATC[C/T]ACACCAAAAACCCAT | 1161 |
rs80295722 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884173 | ATTCAAACCCAGTTT[C/T]CTGAAGCTAAAGACT | 1161 |
rs111231113 | snp | A/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930454 | CCCAGCTACTTGGGA[A/G]GCTGAGGTAGGAGAA | 1161 |
rs111263480 | in-del | -/A | 0.0930568 | 0.194599 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894603 | AGGCTCAGCAGTGTG[-/A]AGCATCACCTGAAGC | 1161 |
rs111266849 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889519 | TTCTGTCACCTAGGC[C/T]GGCCTGGAACTCCTG | 1161 |
rs111316235 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891703 | CTTTTATTTCTGTTG[G/T]AAAACAGAGTAGGGG | 1161 |
rs111374237 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935259 | TTACCTCCCTGGCTA[A/G]GTATATTCCTAAGTA | 1161 |
rs111390120 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907532 | TAATTTTTGTATTTT[A/T]AGTAGAGATGAGGTT | 1161 |
rs111401795 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892545 | TCCTGACTGTGTAAG[C/T]CTCTCTTCTTCCCCA | 1161 |
rs111549620 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886066 | TATGTATATATATAT[A/G]TATATATATACAAAC | 1161 |
rs111554648 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934758 | AGGTGAGAGATGAAG[A/T]TCCATTTTCATTTTC | 1161 |
rs111586807 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916754 | ACACAACACTGTTTT[C/G]TTTTGCTCACTAGAA | 1161 |
rs111601333 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883731 | GATTCTTAGTGAGAG[G/T]TCAGGTTTAAACTGG | 1161 |
rs111621755 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931770 | TACAACAGAATATAT[A/G]CTCTTTGTAACAAGT | 1161 |
rs111675358 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892668 | AAGATGGTCTCCACT[C/G]GGGTCATGGGGTCTG | 1161 |
rs111716838 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60880116 | ATTTTATTTCTCCTT[A/C]ACTTACGAAGCTTAG | 1161 |
rs111780469 | snp | A/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930936 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 1161 |
rs111837193 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938377 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 1161 |
rs111910810 | in-del | -/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891663 | TGGGGGGGCATATTC[-/T]TTTTTTTTTTTCCTG | 1161 |
rs112082196 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926632 | GTTCAGTTACTCTAA[C/T]TGTGTACATAGAGAA | 1161 |
rs112104590 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902779 | TTTAAATACAGTTGT[A/T]AGCTTATGTCAGTAA | 1161 |
rs112107300 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880946 | AGAGGTGCTCTGACT[C/T]TTAGAGTTTCCAGTT | 1161 |
rs112108713 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928122 | CTAATTGTAGGCCAC[A/G]TGAAAGGTTTTGTAC | 1161 |
rs112188002 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894263 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 1161 |
rs112240339 | in-del | -/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891567 | CTACCCCACCAAGAA[-/T]TTTTTTTGGGGCTAA | 1161 |
rs112269808 | snp | C/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913215 | CGGTTGTGAATCCGT[C/G]TGGTCCTGGACTTTT | 1161 |
rs112297102 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923097 | GGAGCCAAACCACTG[A/G]AGCCTTACTTTTGGG | 1161 |
rs112338571 | snp | A/T | 0.172997 | 0.237846 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933238 | TTTTTTTTTTTTTTG[A/T]GACGGAGTCTCACTC | 1161 |
rs112384944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923528 | GAAATAACAATAGTT[C/G]ATGAGGTATATGATA | 1161 |
rs112391630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909003 | TCAGTATAGTCATTA[C/T]ATGACAATGTGAAGC | 1161 |
rs112555472 | snp | A/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893119 | TGTTGCCTTCTGCCC[A/G]TAGGATAGCCTCCCC | 1161 |
rs112613959 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896075 | CACCGCAACCTCTGC[C/T]TCCCAGGTTCAAGTG | 1161 |
rs112726900 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885221 | GTCTTTCTATGTTGC[A/G]TAGGCTGGTCTTGAA | 1161 |
rs112804303 | in-del | -/TTTCT | 0.126909 | 0.217598 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895977 | AATGTCATATTAATA[-/TTTCT]TTTCTTTTCTTTTCT | 1161 |
rs112808360 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874425 | TCAAGGAACACATTT[G/T]GACTAAATAAACTAT | 1161 |
rs112829811 | snp | A/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899528 | AAAATCATAAAGTTT[A/G]CAATTTGTCAATATG | 1161 |
rs112903442 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879859 | TGGAGCAGTTAGCCC[A/T]TTTACATTTAAGGTT | 1161 |
rs112918297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60902862 | TTAAAGGATAAAAAT[A/G]TTTTCCAATTTCTCA | 1161 |
rs112931626 | snp | A/G | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908697 | AAGAAGCAGAGAAAA[A/G]TCATGACATTATAAA | 1161 |
rs112941214 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885155 | TAGCTGGAACTATAA[C/G]TGTAAAGCCACCAAA | 1161 |
rs112995266 | snp | C/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888116 | CCCTCCCCAACAAAA[C/T]CGAAGAAATATGTTA | 1161 |
rs112997008 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878738 | TATCATTTTTTTTGC[A/G]TCTATTTGATTCTGC | 1161 |
rs113034477 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892657 | TGCAGCACTGCAAGA[G/T]GGTCTCCACTGGGGT | 1161 |
rs113231890 | snp | C/T | 0.5 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915187 | TTAGAATAACTTACT[C/T]GTAAAGGCACCTAGG | 1161 |
rs113277991 | snp | A/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918352 | AGGATACCACTGTAC[A/G]GTCTCCACACTGTAT | 1161 |
rs113459006 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926132 | ACCCGGCCTGTCATC[C/T]TTCAAGAATGGCACC | 1161 |
rs113518997 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937825 | TCCGCTTTCCTGGAG[C/T]GTTCCTGTGGTAGTT | 1161 |
rs113549747 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934487 | TAGTCCTCTGTTGGA[C/T]GTATAGGTTGTGAAG | 1161 |
rs113581007 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945629 | ACCCAGCGCCTTCCC[C/T]CGGCGTGCCCCGGGC | 1161 |
rs113584058 | in-del | -/T | 0.0930568 | 0.194599 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896377 | CCCACCACTGGCTAA[-/T]TTTTTTGTATTTTTA | 1161 |
rs113694747 | snp | A/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918295 | ATCCCATACTTTCAG[A/G]GTTTTATCAAATGAG | 1161 |
rs113790817 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60943001 | TTTTAGGCTGTGTGG[C/T]AGCTCGCACATATAA | 1161 |
rs113937386 | snp | C/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933221 | CCTTTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 1161 |
rs113995393 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898842 | AGTCTCAAAATTTAT[A/G]TCACTTACAAAATTA | 1161 |
rs114005053 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885779 | AGTAAACCTTAGCAG[C/T]TGAAAATTTAGGTAT | 1161 |
rs114032592 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938649 | GTGAGCCACAGCGCC[C/T]GGCTGAATTTGTTAA | 1161 |
rs114254462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926346 | GCTCCTTTAAATGGT[A/G]TGTGTAATGATGTAG | 1161 |
rs114353081 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908891 | TGTGAAATACCTTTG[A/T]CCTCTTATTGAAAAT | 1161 |
rs114434119 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900959 | ACATTCTAGACCTTG[C/T]TGCACTTCAGAAATC | 1161 |
rs114579493 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941646 | TTAAACTGCTGAAAA[C/T]TAAAGACGAAGTCTT | 1161 |
rs114641973 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882260 | AGTAGAAAAAGTTAC[A/G]TGTTCCTAGTACATT | 1161 |
rs114659579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884976 | AAACTATCACTATAA[C/T]GACATAACAAGGAAA | 1161 |
rs114691972 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921150 | CATGTATACTGATTT[C/T]TAAAATAAAATAATG | 1161 |
rs114730525 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936496 | TTATCTTTTGTGTTT[G/T]GTTGTTGTTGTCCTT | 1161 |
rs114918855 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935161 | ATTGATTCTACCCAT[C/T]CAAATGTAGAATTTA | 1161 |
rs114997438 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883421 | AACATCTCCTCCTAG[A/T]GGACATGCAGTCTGT | 1161 |
rs115033096 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929190 | AGACGGAAATTTGTA[C/T]GAAAAAAGTTAAATT | 1161 |
rs115135375 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941792 | CTTCAGAGACAAGAA[A/C]AAGATATAAGAAGGA | 1161 |
rs115153681 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924923 | AACATTATTCTCTCA[C/T]TTATTATATGTTTAT | 1161 |
rs115161674 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918946 | TTGAAGACTCTATGA[C/T]GTCAGCTACAATACA | 1161 |
rs115224412 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875340 | TAACACGTTTATAGT[C/G]AGCACATAGGTTTCC | 1161 |
rs115259331 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897253 | AACAGCAACTCCAAC[A/G]TCCCAGTATTTCCTG | 1161 |
rs115291910 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931790 | TTGTAACAAGTAAAA[A/G]CAGTATCATTCAAAC | 1161 |
rs115483964 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900991 | TAAATTTCAACATCA[C/T]ATTCTGCCAGTTATT | 1161 |
rs115492583 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915194 | AACTTACTCGTAAAG[G/T]CACCTAGGCCTGGAG | 1161 |
rs115607471 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885107 | AGCCTTGAACTCTTG[C/G]GCTCAGTGATCCTCC | 1161 |
rs115720669 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919566 | AAATACAAGAACTAT[A/G]GTGCCTACTCATATT | 1161 |
rs115861311 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942680 | ATAAATGACCGTCAA[A/C]AATTTTTTAGGGTTA | 1161 |
rs115886084 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910086 | AGGCTATTAGTAGTT[A/G]AGCTTTTGGGGTAAT | 1161 |
rs116150598 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946421 | GATTTATCACTCAAT[C/T]AATTTATTTTTGCCT | 1161 |
rs116153638 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938512 | GCGTGTGCCACCACA[C/G]CCGGCTAATTTTTGT | 1161 |
rs116180524 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899408 | TTCTACTTTTGAAAA[G/T]TTGGGGGCAAATGAA | 1161 |
rs116232323 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892115 | GTACTGGGCAGCAGT[A/C]CACTGGGCACACATC | 1161 |
rs116250584 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944016 | AAGTAAATATCTTCA[C/T]AGGTTCCTCAATTAA | 1161 |
rs116255739 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908310 | TCAAATTTTGAACTT[A/C]TGGATTAGGGACACT | 1161 |
rs116295407 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880865 | CCTTTTTTCTCAACT[C/T]GTCAATGTCATTCTC | 1161 |
rs116412433 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905498 | CCACTTGTCAAGACT[C/T]CACCCTGGGTGACCC | 1161 |
rs116651259 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923669 | TTTTTTTACAAGACA[A/T]AATTCTCCTTGAACA | 1161 |
rs116706290 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909910 | AGTGAGCTGAGATTG[C/T]GCCACTGGCCACTGC | 1161 |
rs116719230 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905300 | TTTCAGTTATCTATG[A/G]CCACAATCTTCTACC | 1161 |
rs116720623 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886984 | ATGACATGAAAAAAG[G/T]CTTATTGTACAATGT | 1161 |
rs116723269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892565 | CTTCTTCCCCAAATG[A/G]TGGGCCACTGCTGTC | 1161 |
rs116787538 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935104 | GATGGAAGTTGCATT[G/T]AATTTGTAGATTGTT | 1161 |
rs116819180 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941075 | TCCCAGTGACTCTTG[G/T]GAAGCTGAGGCAGGG | 1161 |
rs117098869 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894937 | GCAGTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 1161 |
rs117278849 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905243 | CTACCACACCCAGGA[C/T]GCTGTCACTACCTAG | 1161 |
rs117295664 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941551 | AAGTTTATGGAAAGA[C/T]ATAAGTCTACAAGTT | 1161 |
rs117415642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895503 | TTCTTATCTGTTAAA[C/T]GGAAATAACATCATT | 1161 |
rs118010688 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942059 | TAGACAACGAAAAGT[A/G]AGTATTTTATAATTC | 1161 |
rs118063318 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914901 | ACATGATGAATTACA[C/T]TAGTTGATTTATAGA | 1161 |
rs121434323 | snp | A/C | | | stop-gained | ERCC8 | GRCh38.p7 | 5:60890964 | TGTTTATACAGTTTA[A/C]TCAGGAGAACAGATA | 1161 |
rs121434324 | snp | G/T | 6.58913e-05 | 0.00573945 | ERCC8, NDUFAF2 | 5 | allele_origin=G(germline)/T(germline) | 5:60944972 | CGCCAAACGGGTTTG[G/T]AGGACCCTCTTCGCC | 1161 |
rs121434325 | snp | C/T | | | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904794 | AGCACTGTTTGGTAG[C/T]AGGTTTGTAAGTGTA | 1161 |
rs121434326 | snp | C/G | 0.000132065 | 0.00812498 | ERCC8 | 5 | allele_origin=G(germline)/C(germline) | 5:60902446 | TATATCTTGGCAACA[C/G]CAAGGTAAAATTTAA | 1161 |
rs137994578 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908846 | CTGTCACTGCAGCTA[C/T]GCCAGCAGGTGTGAA | 1161 |
rs138039154 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946235 | TGGGTTAGAATCTCA[G/T]CTTTGACACCTGATA | 1161 |
rs138069005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897222 | TAGTGAAGCCTACCC[C/T]GACTTCCCTATGTGA | 1161 |
rs138078636 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944337 | CCACTCTTGTTCTCA[A/G]TTGCAACCCATTCTC | 1161 |
rs138096094 | snp | C/G | 1.65086e-05 | 0.00287298 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928930 | ATTCTTTCAACATCT[C/G]TGTCTTTATTTAATT | 1161 |
rs138171418 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938762 | TAAAGTCATGTATCT[A/T]CTAAATCTAGTTTGT | 1161 |
rs138173863 | snp | A/C/T | 0.000498057 | 0.0157731 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60890907 | GAAATTTGACTGAAA[A/C/T]ACACAGCAGTCAACA | 1161 |
rs138212997 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903505 | AATAATGCACAGAAG[G/T]ATCTTTATTTCCCTG | 1161 |
rs138234622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923019 | GCCCATTCTAGGAAC[C/T]AAAAGAAGGGATTTG | 1161 |
rs138333261 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885601 | GACACCAAAAGCAGC[A/T]GTATGCTAAAGTTAA | 1161 |
rs138338069 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916302 | TCATTTATCTGCCTC[G/T]TAGAAGCTATCCAAT | 1161 |
rs138433866 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903913 | ATATTTTAGTAGTAA[C/G]AGACCTCTATTATTA | 1161 |
rs138442145 | snp | G/T | 0.21875 | 0.248039 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879168 | TTCAGTTTCCATGTA[G/T]TTGAGCGGTTTTGAG | 1161 |
rs138486280 | snp | C/T | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919833 | TATAGTGAAGATTTG[C/T]ATTAGGTTAGGCTGG | 1161 |
rs138505352 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915819 | AATTCAGTATTATCT[A/C]CCTGTCTTGAGGTCA | 1161 |
rs138683353 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928012 | ATAACACCAAAAACT[A/G]TTTCCTTTAGTTAAT | 1161 |
rs138733994 | in-del | -/ATTT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938090 | ATATATATATATTTT[-/ATTT]TTTTTTTTTTTAGGT | 1161 |
rs138752036 | snp | C/T | 0.000202007 | 0.010048 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60874666 | AAAGGCCGGATTTAA[C/T]TGTGATTTTGTTGTA | 1161 |
rs138752856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934867 | TTGCTGAAGATCAGC[C/T]AGCTGTAAGTATTTG | 1161 |
rs138915352 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884250 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCATGAGG | 1161 |
rs138952755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875560 | TAAAGTAATTGGGTA[C/T]TATGAGCCAGGTTTG | 1161 |
rs139010991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909883 | CACTTGAACTCAGGA[C/T]GGGGAGGTTGCAGTG | 1161 |
rs139084645 | in-del | -/G | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943594 | AGATAAACCCACATG[-/G]GAATTTTACAGATTA | 1161 |
rs139125021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935856 | TATGGACTTGCATAT[C/G]TTAAACCATCCCTGC | 1161 |
rs139195959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921487 | AAAAAAAATTATCAC[A/C]AGATTGGTAAGCCAG | 1161 |
rs139218655 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918134 | CTCAAGTAGTCTAGC[G/T]CTTCTTAACCACTGT | 1161 |
rs139305845 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906812 | AACTAAATGTCTTCC[A/G]AAGTTAGCTTGGCCA | 1161 |
rs139365184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927314 | AGTTATATACACATC[A/G]ATTTTTTTAGTTTTC | 1161 |
rs139404920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899859 | CATACATTAGGGTTG[C/T]TGAACTTTTGCCTTT | 1161 |
rs139419435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940710 | GCATACACCTGGGGA[A/G]GATCTGAAGAGACTT | 1161 |
rs139440197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893138 | GATAGCCTCCCCCAT[C/T]TGGAAGCAGCAGCAG | 1161 |
rs139458408 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937590 | GGGAAGGCCGGCAGC[A/C]AAAGGCTTCACCCAG | 1161 |
rs139548618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887019 | GAGAAAAGTGAGATA[C/T]CAAGTTGAATGTCCA | 1161 |
rs139590259 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889744 | AAGGAGGGACAATGT[C/T]TTAAGAATTTCTTTG | 1161 |
rs139625515 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906762 | AAATAAATAAATAAA[C/T]AAATACATACATAAA | 1161 |
rs139678760 | in-del | -/G | 0.0275645 | 0.114116 | intron-variant | ERCC8 | GRCh38.p7 | 5:60943039 | ACTTTAGGAGGCAAA[-/G]GCAGGAGGATCACTT | 1161 |
rs139800798 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879748 | TCCCTTTATTTTCAG[C/G]CTATGTGTGTCTCTC | 1161 |
rs139901843 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925102 | ACCTTAATCCTATTC[C/T]TTTGCTCATTTTTAT | 1161 |
rs139968741 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875855 | ACGCCTGCCACCACG[C/T]CTGGATAATTTTTTA | 1161 |
rs139988049 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928731 | TTGAAATTAATAATG[A/C]CAGATTCAAAAATGC | 1161 |
rs140185830 | snp | C/T | 3.32259e-05 | 0.00407576 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60903652 | AATAAAAATACCCTG[C/T]AGAATGTGAGAACAG | 1161 |
rs140196641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905631 | CAACTACTCATCTCT[A/G]TCACTGCAGTGTTAA | 1161 |
rs140228606 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926013 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCACGT | 1161 |
rs140286564 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878385 | ATGATGCTGACCTCA[A/T]CAAATGAGTTAGGGA | 1161 |
rs140299416 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908676 | AGTGATGCTGCAAGT[C/G]GTACCAAGAAGCAGA | 1161 |
rs140343389 | snp | A/T | 0.000382133 | 0.0138174 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922154 | AACCACCTGATAACA[A/T]GCTGATAATAAAAAA | 1161 |
rs140432470 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896007 | TTTTCTTTTTTGAGA[C/T]GGAGTTTTCGCTCTT | 1161 |
rs140606758 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913285 | ACCTGTTATTGGTCT[A/C]TTCAGAGATTCAACT | 1161 |
rs140669734 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930888 | AAGGAGGCCGGATCA[A/C]TTGAGGTCAGCGATT | 1161 |
rs140803801 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917065 | TGAAATCACTAAACT[A/G]CATGATAGAACTAAA | 1161 |
rs140843015 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912601 | TTTCTCTTGCCTGAT[G/T]GCCCTGGCCAGAACT | 1161 |
rs140947745 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915137 | TTCCTCTTGAAGCAT[A/T]TGTATAAGATTGGTA | 1161 |
rs141015005 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919089 | GAGAGATTTATGAGA[C/T]GAAGAGGGAAATTTG | 1161 |
rs141030097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937826 | CCGCTTTCCTGGAGC[A/G]TTCCTGTGGTAGTTC | 1161 |
rs141118419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920402 | ACTTATATTTTAAGT[G/T]TAAATTTTAAAATAG | 1161 |
rs141137570 | snp | C/G | 4.95176e-05 | 0.00497558 | missense | ERCC8 | GRCh38.p7 | 5:60898338 | CTGTACCAACAGTGA[C/G]GAGGTGAAGTCCATC | 1161 |
rs141156910 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915825 | GTATTATCTCCCTGT[A/C]TTGAGGTCAGGTGAT | 1161 |
rs141247384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892593 | GTCAGAAAGTGCTCA[A/G]TAGTCTGGTACCCAG | 1161 |
rs141296306 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894498 | CAGACCATAAATAGT[A/G]TGTACACTGTAGTTT | 1161 |
rs141315347 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891385 | AAAAATTAAAAAAAC[A/G]TAAGACATTAGTGAT | 1161 |
rs141491348 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881613 | TTGATCTCAGACTGC[C/T]GTGCTAGCAATGGGC | 1161 |
rs141492697 | snp | A/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945305 | GGAGATCGCTGTCAA[A/G]GGAAGTGAAGGAGCA | 1161 |
rs141584398 | in-del | -/T | 0.24019 | 0.249807 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911775 | TTTTTGTATAAGGTG[-/T]TAAGGAAGGGATCCA | 1161 |
rs141619644 | snp | A/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946873 | TTTCTAGAATATCAT[A/G]TAAATGGAATTATAC | 1161 |
rs141645867 | in-del | -/TTCAG | 0.49823 | 0.0296997 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905286 | TTTGAAATCATACAT[-/TTCAG]TTATCTATGACCACA | 1161 |
rs141720590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927337 | TAGTTTTCCACAGAA[C/T]GTACGCTTTCCTTTT | 1161 |
rs141845482 | snp | C/T | 0.000713142 | 0.0188696 | missense | ERCC8 | GRCh38.p7 | 5:60890918 | GAAATACACAGCAGT[C/T]AACAGTTTTATAATG | 1161 |
rs141898557 | snp | A/G/T | 0.000362485 | 0.0134581 | stop-gained, synonymous-codon | ERCC8 | GRCh38.p7 | 5:60887494 | CCAAGCCAGAATGTT[A/G/T]CAGTCTCTGCTACCA | 1161 |
rs141901721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932047 | CTACTTCCTCAACCT[A/G]CTCAGGCTCTGAAAT | 1161 |
rs141916749 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927695 | TCCAAACCCAAAAGT[C/T]AGCTATCTCCTGCTG | 1161 |
rs141936115 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934504 | TATAGGTTGTGAAGA[C/T]TTTCTTCCACTCTGT | 1161 |
rs141954512 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911397 | CATAAATGTCTTCTT[C/T]GAGAAGTGTCTCTTC | 1161 |
rs142090036 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883132 | CAAAATTATACTTCA[A/T]CATAAATTATTTTTG | 1161 |
rs142093470 | in-del | -/AAAT | 0.441432 | 0.160792 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906731 | AAAACTCTGTCTCAA[-/AAAT]AAATAAATAAATAAA | 1161 |
rs142133488 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893982 | TGCTCCTGGGAATTT[-/A]TCTTTTTTTTTTTTT | 1161 |
rs142139247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903521 | ATCTTTATTTCCCTG[C/T]TGAGTCTCAACAACC | 1161 |
rs142282347 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876759 | AAATTTGTTTGAGTC[C/T]ATTGTAGGTTCTGGA | 1161 |
rs142297679 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911139 | ATAGGTATATATGTG[C/T]CATGTTGGTTTGCTG | 1161 |
rs142306167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908525 | ATATAATCCACCCAA[C/T]TGTCAAGCCAGAGAA | 1161 |
rs142397458 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941609 | ATAAATCCAAAGAGA[A/T]CTGCAACCAGACACA | 1161 |
rs142431216 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890252 | TCAGTATTTAACTTA[C/T]GTGAGTTTCATTTTC | 1161 |
rs142510967 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881319 | ATCAGGGACCCACTT[A/G]AGGAGGCAGTCTGTC | 1161 |
rs142537648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929416 | CCCCAGGCAACATAG[A/C]GAGACCCCATCTCTA | 1161 |
rs142645894 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924834 | TAAGTTTTAGTCAGT[C/T]TTCATTTCTGAAATA | 1161 |
rs142663165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884003 | TCAGGAGAAACACCC[C/T]TAAGGGATTACATCT | 1161 |
rs142727106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940444 | GGCCTAAACTTGGAA[A/G]CGTATGGCAGAACAG | 1161 |
rs142734684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886394 | ACTGGTAAAATTTGA[C/T]GTGAGAACAAAGTCT | 1161 |
rs142788898 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902138 | TAACTCCAGGTTAAA[G/T]ATAATGAATAAAAAT | 1161 |
rs142812882 | snp | A/C/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945983 | TATCCCCACAAGGCT[A/C/T]GCTGATTCCTTTCTC | 1161 |
rs142813194 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917488 | TTTATAATAAGATTA[A/C]TTCTGGGGTAGAACT | 1161 |
rs142838100 | in-del | -/T | 0.498277 | 0.0293024 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908581 | ATATATATATATATA[-/T]TATTTTTTTTTTAAA | 1161 |
rs142953813 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884473 | AGAGCCAGACTCCTT[C/T]TCAAAAAAAAAAAAA | 1161 |
rs143039108 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878773 | TTTTCTTCTTTATTA[C/G]TCTTGCTAGTGGTCT | 1161 |
rs143126203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908545 | AAGCCAGAGAACCTG[C/G]GGGTCATTCATATAA | 1161 |
rs143139297 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933217 | TTTTCCTTTTTTTTC[-/T]TTTTTTTTTTTTTTT | 1161 |
rs143147836 | snp | A/G | 1.67691e-05 | 0.00289556 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60874645 | ACTGCTGCTCCAGGC[A/G]TCTTCAAAGGCCGGA | 1161 |
rs143157714 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917317 | AACAGATTCAAAACA[C/T]GATCAGTTTAGTTGC | 1161 |
rs143221570 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922424 | GTGACAGAAACAAGA[C/T]GGCAAAAGAGATTTC | 1161 |
rs143255688 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944969 | GAAGGCGAAGAGGGT[C/T]CTCCAAACCCGTTTG | 1161 |
rs143267182 | in-del | -/TCAG | 0.23846 | 0.249734 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881151 | CCGTTTGCCTGGCTA[-/TCAG]CTCAGAGACTGCAGA | 1161 |
rs143272520 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934105 | GGTGGATACCCGGGA[A/G]TGGGAATGCTGGATC | 1161 |
rs143356896 | snp | C/T | 0.000264432 | 0.0114955 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928855 | ATTATACAAGTATAA[C/T]AAACTTACTATCTCC | 1161 |
rs143358449 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881328 | CCACTTGAGGAGGCA[C/G]TCTGTCTGTTCTCAG | 1161 |
rs143361332 | snp | C/G | 0.030278 | 0.119257 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877219 | ACTTCTGAGGGCTCT[C/G]CTCTGTTCCATTGGT | 1161 |
rs143367518 | snp | C/G | 4.9703e-05 | 0.00498488 | stop-gained, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918364 | TACAGTCTCCACACT[C/G]TATCTGTGAACATCA | 1161 |
rs143403640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925204 | AACATCCTCTTCTTC[C/T]CTTAAAAATTTTTTT | 1161 |
rs143459063 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919719 | ATAAATTAAACTAGT[A/G]GAAAAATGAACATGA | 1161 |
rs143686695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884951 | AAAAGTTTGTTTACA[C/T]GAAGAGTTCAAACTA | 1161 |
rs143783797 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905723 | CACAAACAAAATCAA[C/T]TCACAAAAACCATGG | 1161 |
rs143935324 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936564 | TTTTTCTTCTGTTGG[A/G]TTTGGGTTTGGTTTG | 1161 |
rs143997890 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909975 | AGAAAAAAAAAAAAA[-/T]AATAATAATAAAAGA | 1161 |
rs144002469 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879203 | TTTCTTAATCCTGAG[A/T]TCTAGTTTGATTGCA | 1161 |
rs144006692 | snp | A/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945365 | ACTACTACATCCCGC[A/T]GTACAAGAACTGGAG | 1161 |
rs144192593 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936928 | AGGGAAGATCTGGGA[C/T]TCAAGGGCTGCTCTG | 1161 |
rs144224808 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931600 | AGGTGTGAGCCACCA[C/T]ATTCAGCCCTGAACT | 1161 |
rs144255695 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923559 | AGTTCAGAGAAAATT[A/C]TGCAAAATGGAGGAT | 1161 |
rs144355002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916857 | GCATTTACTCAGCAG[C/T]TACTGTACATAGCAC | 1161 |
rs144440143 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904956 | TTACTTTTTCCTAAA[A/T]TTTTAGCTATTTTTA | 1161 |
rs144604076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915674 | TTGGCTTGTGATCCC[A/C]TTAATCCATCTTCAA | 1161 |
rs144623976 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909094 | ATTTTTGGAAAGTTT[C/T]GGCTTTAAAAAAGTC | 1161 |
rs144636838 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907609 | TGTCAATCCCCCTAC[G/T]TGTGTTCAGATTCCC | 1161 |
rs144637956 | snp | A/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919233 | ATAGGTTGTTCGAGA[A/T]TTGCTTCAACATAAT | 1161 |
rs144950639 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878656 | TTTCTAGTTTATTTG[C/G]ATAGAGGTGTTTATA | 1161 |
rs144954296 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931784 | TGCTCTTTGTAACAA[-/G]TAAAAACAGTATCAT | 1161 |
rs145014758 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890005 | GCTGAGGCTGGAGGT[A/C]GCTTGGGGGCTTGGT | 1161 |
rs145033374 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895811 | CATTTGTTTCTCAGG[A/C]CACCTAGTTATAAAA | 1161 |
rs145052120 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883742 | AGAGGTCAGGTTTAA[A/C]CTGGAATAAACCTGC | 1161 |
rs145102087 | snp | C/G | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873764 | TTTACTAGTCTACTG[C/G]TGGTAAGGATCAGGA | 1161 |
rs145230004 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874279 | GTCAATACTGATGGC[C/T]TCCACTTGCTGATCC | 1161 |
rs145297130 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878480 | CCTCTGGTAGAATTC[A/G]GCTGTCAATCCATCT | 1161 |
rs145298549 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933323 | TCCCAGGTTCAAGTG[A/G]TTCTCCTGCCTCAGC | 1161 |
rs145397278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941122 | GGAGTTCAGGACCAG[C/T]CTGGGCAAAACAGTG | 1161 |
rs145485047 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880958 | ACTTTTAGAGTTTCC[A/T]GTTTTTCTGCTCTGT | 1161 |
rs145518936 | snp | A/G | 0.000148492 | 0.00861532 | synonymous-codon, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928908 | GGTGTTAATTCCACC[A/G]CCGTGGATTCTTTCA | 1161 |
rs145610983 | snp | A/G | 3.30846e-05 | 0.00406709 | missense | ERCC8 | GRCh38.p7 | 5:60903689 | GACTTCAAGTCACAA[A/G]GTTGTACTTTGGGTC | 1161 |
rs145620659 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937709 | ACTTGCCCCAGGCTT[C/T]AAGCCACCCAGCTGA | 1161 |
rs145633982 | snp | A/C/T | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914168 | CTTCAGTCTCATTGA[A/C/T]CTGTCTAATGTTGAG | 1161 |
rs145637736 | snp | A/G | 0.000153988 | 0.00877328 | missense | ERCC8 | GRCh38.p7 | 5:60887514 | CTCTGCTACCACTAT[A/G]AAGTTCCTATAACAT | 1161 |
rs145750707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901423 | AAGTGCCCAGTAATC[C/T]TATGGGCCCTTAATC | 1161 |
rs145754845 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938135 | ATTGAATATAAGTTT[A/C]TCTGGGTCCCCTAAG | 1161 |
rs145850283 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893612 | GATAGGTTCGAATCC[A/G]CTTGCTCTCTTCCTA | 1161 |
rs145913455 | in-del | -/AAAAAAAAAAAC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940253 | ACTCTGAAAAGTAAA[-/AAAAAAAAAAAC]CAGCCACAGACAATC | 1161 |
rs145991531 | in-del | -/GG | 0.0154538 | 0.0865337 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893218 | ATTCTACCACCTCAC[-/GG]ACTCCTTGTAATAAG | 1161 |
rs146144509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905314 | GACCACAATCTTCTA[A/C]CATTTTCAGCTTTTC | 1161 |
rs146449543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914382 | TTGTTGGTTTAAAGT[C/G]TGTTTTATCAGAGAC | 1161 |
rs146500576 | snp | C/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918929 | CATAAAAACATAACA[C/T]GTTGAAGACTCTATG | 1161 |
rs146581468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943381 | CACAGTTTATTAACC[A/G]TGAGAAATAGCATAA | 1161 |
rs146687797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925396 | TGTACTGGGGGCGCA[C/T]TTTGACTGGTTAGCT | 1161 |
rs146700579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919344 | GTCATTATACAACTC[C/T]CCAATCTTGTATATG | 1161 |
rs146740678 | snp | A/G | 0.000132282 | 0.00813163 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922079 | AACACACTGCTTTAC[A/G]TGTGTAATAAGATTG | 1161 |
rs146752966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920772 | CGCATTTACTTATGT[C/G]ACAAACCAAAACAAA | 1161 |
rs146756346 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880674 | GCTACTGAGGCTTGA[A/G]CATTCATCACGTAGT | 1161 |
rs146821208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895918 | CCAGGGCATTAACTT[C/T]TGTCTTGTCCTTAGG | 1161 |
rs146860724 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942673 | AGGGATTATAAATGA[A/C]CGTCAAAAATTTTTT | 1161 |
rs146983649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896785 | CCAAAGGGCATGAGA[C/T]TCACCTTCAAGAAGG | 1161 |
rs147087674 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933160 | GTTTTAAATGGCTTT[C/T]ATAGGATGTATATTA | 1161 |
rs147097126 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927455 | AAAGCGGAAAATCAC[C/T]GTAGCAAGAGTCTTC | 1161 |
rs147156597 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897685 | ATAAAGTACTACATA[C/T]TCTGGTACTATAAAA | 1161 |
rs147167962 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892771 | GAGCATCCAGCAGCC[A/G]GATGAACTTGTCCAG | 1161 |
rs147273502 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876412 | TAATGGGATGGCTGG[A/G]TCAAATGGTATTTCT | 1161 |
rs147370726 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946065 | TAATCATGGTGTTAC[C/T]GTGTAGGATTCGTGC | 1161 |
rs147371359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889456 | GACTACAGGCATATA[C/T]CACCACACCTGGCTG | 1161 |
rs147381360 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940522 | CCCAGAGAACTGGGA[A/C]GCATCCAGGAGATCA | 1161 |
rs147414474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892610 | AGTCTGGTACCCAGA[C/G]AGAAGGTAATAGTTG | 1161 |
rs147474400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922458 | AGAAAGTAAAATATT[A/G]CAAAGTTATTTTAAA | 1161 |
rs147483883 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917436 | TTTAGACAATGGGAA[G/T]CCCTAGAGGGTTTGG | 1161 |
rs147517431 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875739 | TCTCACACTGTCGCC[A/C]GGGCTGGAGTGCAGT | 1161 |
rs147573573 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890066 | ATAAATATTTATATA[C/T]TTTAATAATGAATAC | 1161 |
rs147635163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907776 | ACAAAGAGCATTTTC[A/G]CCCTACATTCTCCCT | 1161 |
rs147740357 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883930 | ATAAATCCTGTCCCT[A/G]TCATCCAGTGTTCTT | 1161 |
rs147784061 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936942 | ACTCAAGGGCTGCTC[C/T]GCAGATTCTTTTGTC | 1161 |
rs147992873 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874361 | GTACAACGACTTGTG[A/T]TACTTGTACTGTAGC | 1161 |
rs148065979 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939639 | ACAGGCACCTGCCAC[C/T]GCACCCGGAGCACGC | 1161 |
rs148225528 | snp | C/T | 0.000352707 | 0.0132751 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898269 | TATATACTTAAAAAT[C/T]TCTTACAAGTGTGTT | 1161 |
rs148241752 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883507 | GTCAATGTTATAGAA[A/G]TAATGAAGCATGAGT | 1161 |
rs148258692 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908649 | ACCTTGGAACCCATA[C/T]GAAGTGTCACTAGTG | 1161 |
rs148331259 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934333 | GCACATCTCTAATCA[C/T]TAGTGATGTTGAGCA | 1161 |
rs148370713 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878783 | TATTACTCTTGCTAG[C/T]GGTCTATCAATTTTG | 1161 |
rs148393161 | snp | C/T | 9.88843e-05 | 0.00703081 | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904792 | AATACACTTACAAAC[C/T]TGCTACCAAACAGTG | 1161 |
rs148427820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929178 | AAAGGTATTTAAAGA[C/T]GGAAATTTGTACGAA | 1161 |
rs148481406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60924372 | CTAAGGAATGGCTAA[C/T]GAGAACAACAGTCTC | 1161 |
rs148550256 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911355 | ATGACGAGTGATGAC[A/G]AGATTTTTTCATGTG | 1161 |
rs148592854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893657 | ATCTGAGAAGAGAGA[A/G]TAACAGACGCTCTTG | 1161 |
rs148635323 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882666 | GGAGTGGTGGCTCAC[C/T]CCTGTAATCCCAGCA | 1161 |
rs148687658 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880372 | TCTCGAGGAGTATCT[C/T]TGTGGCATTCTCTGT | 1161 |
rs148706681 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876692 | TCTTTTGAGAAGTGT[C/T]TGTTCATATCCTTCG | 1161 |
rs148796991 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890187 | TGAATGAATAGGAGA[C/T]TCAAAGTGATAGTCT | 1161 |
rs148807207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941319 | TAACAGATTGGAGAT[A/G]GCAGAGGAAAAAATC | 1161 |
rs148964292 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901570 | GAGAAGCCGTTAAGT[C/G]TGAGTTTCTTGAGCT | 1161 |
rs149077238 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873831 | TGGGTTGACACAGAC[A/G]GAGACAATAACATAG | 1161 |
rs149130938 | snp | C/T | 0.00202427 | 0.0317496 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944943 | TTACCTCCGTGTTGA[C/T]TCTGCTCTCCGAAGG | 1161 |
rs149301862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888762 | TATGAGAGTAAGTTG[C/T]CAACATTAGGCCTTA | 1161 |
rs149353172 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892082 | GTTGTAGGGGGTCCA[C/T]CTCCATGATCCTCTG | 1161 |
rs149608271 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916321 | AAGCTATCCAATGCC[G/T]GTCTTCTCAGTCTCT | 1161 |
rs149662271 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880947 | GAGGTGCTCTGACTT[C/T]TAGAGTTTCCAGTTT | 1161 |
rs149670262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893455 | GGCATGATCATTGGA[A/G]TGAACAAACTGAGGA | 1161 |
rs149732998 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913339 | GGTGTGTGTGTCGAG[G/T]AATTTATCCATTTCT | 1161 |
rs149875193 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926077 | TAATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 1161 |
rs149884683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940786 | TTCTTGTAGCCTGAA[C/T]CTAATCTTGCTAATT | 1161 |
rs149925308 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882031 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 1161 |
rs149928831 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918581 | AGGCTCCCACTGTGT[C/G]ATGTAGAGACATACC | 1161 |
rs149998094 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907291 | TTACCAACAAACCTA[C/T]AAACACATTTGCTTC | 1161 |
rs150200616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944327 | AACTTGGCTCCCACT[C/T]TTGTTCTCAGTTGCA | 1161 |
rs150243260 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884111 | TGATATTTGGAAATA[C/T]TATAAGCTTGTCCCA | 1161 |
rs150260438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875230 | TATTAAGTAGTGATA[A/T]TTATGTACTTATTTG | 1161 |
rs150312684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908759 | ACTGAAGTGTGCAGC[A/T]GTGGTTGCCCACCAT | 1161 |
rs150371740 | in-del | -/G | 0.0123036 | 0.0774623 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946891 | AAATGGAATTATACA[-/G]GATTTAGACTTTTGA | 1161 |
rs150461345 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891189 | GCTATAAAAAGGGCT[C/T]TTTTAAATTTAAGGA | 1161 |
rs150474378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60916113 | TCTTAAGTCTATGGT[C/T]TCGCATAGCTTGGTC | 1161 |
rs150519720 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946995 | AGTAGTATTCCATTG[C/T]ATGGGTTTGCCAGTT | 1161 |
rs150573288 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939805 | CTTGTTAGTAGGTAT[A/C]ATTCCAGTGTTTTCT | 1161 |
rs150632283 | snp | A/C/G | 3.3082e-05 | 0.00406696 | missense | ERCC8 | GRCh38.p7 | 5:60890971 | TCTCCTGAGTAAACT[A/C/G]TATAAACAGCAATGG | 1161 |
rs150633142 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912498 | GATTTTGGGCTCAGA[C/T]GATGGGGTTTTCTAG | 1161 |
rs150642110 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927736 | CATGTTTCATAAGTG[A/G]GTGCCCCCCCAGCTG | 1161 |
rs150727525 | snp | C/G | 0.00353859 | 0.0419139 | missense | ERCC8 | GRCh38.p7 | 5:60899690 | TCAAACATCCTGATG[C/G]TCTTCTCACATCCCA | 1161 |
rs150798373 | snp | A/G | 0.00995793 | 0.0698556 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935797 | TCTATTGAGATAATC[A/G]TCTGATTTTTGTTTT | 1161 |
rs150889405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905770 | TTAACTGATGCAAGG[C/T]TGGCCAGGCCAAGTG | 1161 |
rs150950141 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880944 | GGAGAGGTGCTCTGA[C/G]TTTTAGAGTTTCCAG | 1161 |
rs150952570 | snp | A/C/T | 0.000412701 | 0.0143597 | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904864 | CCTCAAAATTAAATA[A/C/T]ATCTGCAGTCTGGTA | 1161 |
rs151003484 | snp | C/G | 0.030278 | 0.119257 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876787 | GGATATTAGCCCTTT[C/G]TTAGATGAGTAGATT | 1161 |
rs151015369 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906764 | ATAAATAAATAAACA[A/C]ATACATACATAAAAT | 1161 |
rs151172196 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883227 | TTTCAGTGAAATAAT[A/G]ATATATGAATGCATT | 1161 |
rs151216334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917786 | ATTTGACCAAATGTC[A/T]TACAAACTATTATCC | 1161 |
rs151328084 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890314 | TCTTGCAATGTTATA[C/G]TCATTTAAAGAAGTG | 1161 |
rs180672445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919187 | CATAAAGTCTTTATC[G/T]TTTAGAGATATAAAT | 1161 |
rs180683744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912161 | AATGGGGATGGTATT[A/C]AATCTATAAATTACC | 1161 |
rs180689364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878488 | AGAATTCGGCTGTCA[A/G]TCCATCTGGTCCTGG | 1161 |
rs180689940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893723 | CAGCCTGGCGGCGCC[C/T]GACTCCGCCCACTGG | 1161 |
rs180694356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930296 | TTAGGCTAGGTGCGG[C/T]GGCTCATGCCTGTTA | 1161 |
rs180782602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883958 | CTTCCTTTCTTTAGA[C/T]AGAATTAAATTCATC | 1161 |
rs181193517 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945746 | GGCAGGGAAAAGTCC[A/G]CGGAAATCTTTCACC | 1161 |
rs181261964 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934389 | TATATCTTCTTTTGA[A/G]AACTGTCTATCCATG | 1161 |
rs181262301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888932 | TTTATAGCAAAAGGG[A/G]CCAGTTAAAAATCAC | 1161 |
rs181262659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881088 | CCTTCTAACAGTCAG[G/T]ACCCTCAGCAACAGG | 1161 |
rs181263515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940139 | TCTTGTTTTATGAGT[C/T]GTGATATTTAATTTG | 1161 |
rs181267882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915559 | AAAATTCTCACATAG[A/G]TCTCAATGGATTATA | 1161 |
rs181270349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925786 | TGTGTTTTAATGGAG[A/G]ACTAGAGGAACATTA | 1161 |
rs181276744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908485 | ATTCCAACCCTTCCC[C/T]ATCTTACTAAATAAC | 1161 |
rs181378530 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893338 | TAGGATATCCTCACA[C/G]TAGCTCTTGATAGAC | 1161 |
rs181384935 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877628 | AGGTATTTTAATCTC[C/T]TTGAAGCAATTGTGA | 1161 |
rs181390025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911459 | TTTTTTCTTGTAAAT[C/T]TGTTTAAGTTCTTTG | 1161 |
rs181444861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929418 | CCAGGCAACATAGCG[A/T]GACCCCATCTCTACA | 1161 |
rs181469435 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907388 | GAGATGGAGTCGCTC[C/T]GTTGCCCAGGCTGGT | 1161 |
rs181500190 | snp | G/T | 1.65399e-05 | 0.0028757 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945393 | GAGAGGTGAGGTGGC[G/T]GCGTGGGCAGCGATT | 1161 |
rs181504429 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896941 | CTCACAAGCCTTTAG[C/T]GGCTTTCCATCTCAC | 1161 |
rs181510783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880707 | TCGTGCCATGGTTTT[C/T]AGCTCCATCAGGTCG | 1161 |
rs181536191 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60873971 | GAGTTCAAGCATTAG[C/T]GCAAACTGCCTTCTG | 1161 |
rs181611227 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888730 | AGTCCAAAAGACTTC[A/T]TTTCCCCCTTGAATC | 1161 |
rs181614083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925394 | TCTGTACTGGGGGCG[C/T]ACTTTGACTGGTTAG | 1161 |
rs181849846 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884252 | TGGGAGGCCGAGGCG[A/G]GTGGATCATGAGGTC | 1161 |
rs181860203 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902199 | CATTTGTGTGTAAGA[A/T]TGACACAACACAGTT | 1161 |
rs181865127 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938678 | AAAGTTTGCTTAGTG[A/G]CCAAGAACAATTTTG | 1161 |
rs181871115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919644 | TTCCTCTCTTACCTT[C/T]ATTATTTTTATAGGT | 1161 |
rs181974408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888325 | TTATCAAATTTCCTA[A/T]ATAAAACAAAATTTT | 1161 |
rs181983798 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906587 | TATAAAAATTAGCTG[G/T]GCGTGGTGGCAGGCG | 1161 |
rs181994701 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944304 | AAGTGTAATCACAAC[A/C]GTTACCTAACTTGGC | 1161 |
rs181994775 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60924292 | ATATTATTGCTCACC[A/G]TCAATCCTTAAGTTG | 1161 |
rs182006009 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877195 | AGATGGTTGTAGATA[C/T]GCAGCATTACTTCTG | 1161 |
rs182053394 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892838 | GGCTCCCACACTGCA[C/G/T]GCATGGCTGTGCTTC | 1161 |
rs182069373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929069 | AGAAATGTCTAAATC[G/T]TCTACCACACATCCT | 1161 |
rs182118892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885421 | ACTGTTTTCATTTGG[C/T]AAATAAAATGTTATA | 1161 |
rs182181227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60916046 | CAATTCTTCTCTCCA[A/G]TACCATGTGACTGGG | 1161 |
rs182272740 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881288 | TGGGGGGTGCCTCAC[A/G]GTTAGGCTACTCGGC | 1161 |
rs182336820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931806 | CAGTATCATTCAAAC[A/G]TGTATAAAGGTAATC | 1161 |
rs182369735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911142 | GGTATATATGTGCCA[C/T]GTTGGTTTGCTGCAC | 1161 |
rs182401243 | snp | C/T | 0.00631138 | 0.0558199 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903575 | CACTTACAAAGAATA[C/T]ACTGTTAGTAACGTT | 1161 |
rs182455886 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935866 | CATATGTTAAACCAT[C/G]CCTGCATTCCTGGTA | 1161 |
rs182456450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936613 | GAGGTATGCCCTTAG[A/G]TTGTCTGTCTGTGCT | 1161 |
rs182540385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898089 | CTAAGTAGGGAGAAT[A/G]TGGTAGGTAGTGGGT | 1161 |
rs182582204 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895511 | TGTTAAACGGAAATA[A/T]CATCATTTACTTATA | 1161 |
rs182590978 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879180 | GTAGTTGAGCGGTTT[C/T]GAGTGAGTTTCTTAA | 1161 |
rs182598035 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913335 | GGAGGGTGTGTGTGT[C/T]GAGGAATTTATCCAT | 1161 |
rs182620233 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931204 | GAGTGGTGATTATTA[G/T]TAAATGCATCTCCTG | 1161 |
rs182646370 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875067 | TGGACTCCAGGTGTA[C/T]AGTCTGACCTGACAG | 1161 |
rs182727728 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881751 | CGATTTTCCAGGTGC[C/T]GTCTGTCACCCCTTT | 1161 |
rs182728037 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940848 | ATAGGATCAAAACAA[A/G]ACCCAGAGTATTCAA | 1161 |
rs182736544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916959 | ACAAGTATGAAAATG[A/G]TATTATAAAGTAGTA | 1161 |
rs182742908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898513 | AGTTACTTAAAAAAT[G/T]TAAGTAGATTATACT | 1161 |
rs182745004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936188 | TTATTACCATTTCAA[C/T]CTCATTGCTTGTTGC | 1161 |
rs182876324 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899480 | TTTAGTTTATGTAAA[C/T]TAAGAAAGTGATATA | 1161 |
rs183067408 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884547 | TTTTTTGTTTTCTAG[C/T]GTGGTATACTGCCTC | 1161 |
rs183077367 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920154 | CTGTGGTGTGACCCT[C/G]ACTGTGTTCTCTATC | 1161 |
rs183189054 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917219 | TGGCATCTACAGTCT[C/T]GGCTCAATGTAATTG | 1161 |
rs183266103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881813 | TTGTGCTTCCCAGGT[A/G]AGGCGATGCCTCACC | 1161 |
rs183292826 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886470 | ACTTTGGGAGGCCAA[C/G]GCAGGTGGATCACTT | 1161 |
rs183305163 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904929 | ATAAAAACAAAGCAA[A/T]AAATTTTCTATTTAC | 1161 |
rs183312768 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942039 | AACAATGAAATGATC[C/T]GAAGTAGACAACGAA | 1161 |
rs183314166 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60922227 | ATTTATGATTGCAAA[C/T]TTCTAAAAACTGATT | 1161 |
rs183319051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902752 | AAAAACAGAGTTAAG[C/T]AAGTCTTTCTTTTTA | 1161 |
rs183414394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889994 | CCAGGGAAGGGGCTG[A/T]GGCTGGAGGTCGCTT | 1161 |
rs183448700 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875536 | AGGGCTTTAAGATGG[A/T]CTCATTGTTAAAGTA | 1161 |
rs183450102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908895 | AAATACCTTTGACCT[C/G]TTATTGAAAATCCAT | 1161 |
rs183465089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882043 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGA | 1161 |
rs183465230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926520 | AGTTATTTGAAGGCT[C/T]AAAAATCCAATTGAT | 1161 |
rs183475533 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946049 | TTAAGAAACGTGGCA[A/G]TAATCATGGTGTTAC | 1161 |
rs183505264 | snp | A/G | 9.03481e-05 | 0.00672056 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60891081 | ACAAACTTTTCCATA[A/G]TTCACCTGTAGGATT | 1161 |
rs183600174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909074 | CAGATAAAGATGGTT[G/T]GATAATTTTTGGAAA | 1161 |
rs183615127 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946690 | CAGTAACATTCACCC[C/T]TTATGGTGTACAGTT | 1161 |
rs183767285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888091 | GCTTATGGCTGAACA[A/C]TGCTCATGCCCCTCC | 1161 |
rs183770478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914061 | GCTGGGAAGAATGTA[C/T]ATTCTGTTGATTTGG | 1161 |
rs183790341 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906336 | CCACTGCTGGGCCTA[C/T]GTTTTAGCAGAATTC | 1161 |
rs183816436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927243 | CCAATCTGATTTTCA[G/T]TGACACCTTTACAGC | 1161 |
rs183870558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894264 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 1161 |
rs183891069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876328 | TGTTGTGAATAGTGC[C/T]GCAATAAACATACGT | 1161 |
rs183902719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891906 | AACTGGTGCTTGGAT[C/T]GGAAGGGAAGTGAGA | 1161 |
rs183917745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909676 | CGCAGTATATAGGCC[A/G]GGCATGGTGGCTCAC | 1161 |
rs183962123 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912854 | ATTGAGATAATCATG[A/C/T]GGTTTTTGTCATTGG | 1161 |
rs183970062 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917438 | TAGACAATGGGAATC[C/T]CTAGAGGGTTTGGGT | 1161 |
rs184027537 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878617 | GGGTGTATGTGTCCA[A/G]GAATTTATCCATTTC | 1161 |
rs184060307 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937148 | TCAGGTCTCTCAGCC[A/G]TGGATACCAGCACCG | 1161 |
rs184122933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900026 | TTCTCCCAAGGACCA[G/T]AAAGGCTTGTAGCTT | 1161 |
rs184144167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879689 | ACTAGGATTACAACC[C/T]CTGCCTTTTTTTGTT | 1161 |
rs184183982 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880772 | GCCATTTGTCTAATT[A/T]TTTTTCAAGGTTTTT | 1161 |
rs184188414 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915195 | ACTTACTCGTAAAGG[C/T]ACCTAGGCCTGGAGA | 1161 |
rs184196708 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897440 | GTCTAATACTGCCTG[C/G]CAAATTAAATGCTAA | 1161 |
rs184199414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934024 | ATATTTTTGCACTTG[C/T]GAATTGTGCTGTTAT | 1161 |
rs184539290 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943419 | CTACTAGCTTTTCAG[C/T]TCACAAATCATTACA | 1161 |
rs184586240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925195 | ATATATTAAAACATC[C/T]TCTTCTTCCCTTAAA | 1161 |
rs184594541 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944537 | GTGTCCTCTGCCTTT[A/T]ATAGGCTGCCTGGCA | 1161 |
rs184616482 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938264 | ATTTCCAAAACATGA[A/G]GTGGTGGTGATGTTA | 1161 |
rs184641277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896000 | TCTTTTCTTTTCTTT[C/T]TTGAGACGGAGTTTT | 1161 |
rs184660447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924171 | GTGCTATAATTTAAA[A/C]TAATTTCTATTTCCC | 1161 |
rs184684420 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882268 | AAGTTACGTGTTCCT[A/T]GTACATTTTCCAAGT | 1161 |
rs184690962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901753 | ATGCACCAATTATTC[C/T]CTCCATTTCTTATCT | 1161 |
rs184693660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917779 | AATGTAAATTTGACC[A/G]AATGTCATACAAACT | 1161 |
rs184698210 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900889 | AAATCCACCCAAGCA[C/T]AACCAGCACCTAGCT | 1161 |
rs184704690 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937652 | TTTCACTCCCACTGC[A/G]CCCCTACAACAGCTC | 1161 |
rs184724192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928618 | CATCCAAAAGAAGTT[C/T]AATGTTTGTTAATTT | 1161 |
rs184743153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918564 | CAGGCATCTCTAGAT[A/T]CAGGCTCCCACTGTG | 1161 |
rs184770801 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923054 | TGGAGCAGTGTGGAA[A/G]GGAAAGAGTGGTGAG | 1161 |
rs184813752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883467 | TCTATATCTCACCAG[C/G]TTGTCAATTCTACTG | 1161 |
rs184872402 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887061 | AACTATGTTAAAAAA[A/C]ATATGCATAGGAAAA | 1161 |
rs184906769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942934 | ATAAAATGGAACTAT[A/G]TAATTGTTTAAGCAA | 1161 |
rs184972008 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905102 | TTTCCCAATAAATCC[A/C]AGAAATTAAGAAAAT | 1161 |
rs185265776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930483 | AATCACTTCAACCTG[A/G]GAGGCGGAGGTTGCA | 1161 |
rs185328534 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877230 | CTCTGCTCTGTTCCA[A/T]TGGTCTATATCTCTG | 1161 |
rs185366743 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911436 | TGCCTACTTTTTGAT[A/G]GGTTTTTTTTTTTCT | 1161 |
rs185413667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934468 | CCTTGAATATTCTGG[A/G]TATTAGTCCTCTGTT | 1161 |
rs185416439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889659 | GCTCCAATTTGGTAG[A/G]AAGAAATAATTTGTG | 1161 |
rs185418251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932817 | AGAGGGAAAAGAGAA[A/G]GGAAAATGGGCAAGG | 1161 |
rs185423188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875194 | GAATAATACCATTTT[C/T]AGTCCAAAAATAATG | 1161 |
rs185431350 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908643 | TCATACACCTTGGAA[C/T]CCATACGAAGTGTCA | 1161 |
rs185443726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926014 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCACGTT | 1161 |
rs185466306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892912 | CAATGTCCATATGGA[C/T]GTGGGTGCGCATTTC | 1161 |
rs185490912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896055 | GCAATGGCATGCTCT[C/T]GGCTCACCGCAACCT | 1161 |
rs185513749 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881752 | GATTTTCCAGGTGCC[A/G]TCTGTCACCCCTTTC | 1161 |
rs185557435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893358 | TCTTGATAGACCTGC[C/G]TTTTTGTCTTTCTTG | 1161 |
rs185564738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892330 | GTCTGTGTCACCCAA[C/T]AGCTCATCAGATTCT | 1161 |
rs185572712 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877688 | GTCTGTTATTGGTGT[A/G]TAAGAATGCTTGTGA | 1161 |
rs185574679 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911615 | TCCCACTTGTCAATT[C/T]TGACTTTTGTTGCCA | 1161 |
rs185592642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929834 | ATTAACTATTTGAAT[C/G]TCTCTTAATCTGTTG | 1161 |
rs185625116 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880401 | GTTTTTCTGAATTTG[A/T]ATGTTGGCCTGACTT | 1161 |
rs185632856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914744 | GTGAGTTATAATTGC[A/G]CCACTGCACTCTAGC | 1161 |
rs185766750 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876773 | CCATTGTAGGTTCTG[C/G]ATATTAGCCCTTTGT | 1161 |
rs185824907 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898557 | AGATTATTTGAATAG[C/G]ATAAGCTATATAAAT | 1161 |
rs185830878 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936369 | GGTTGTAATATCTCC[A/C]ATTTTGTTTCTAATT | 1161 |
rs185971379 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902246 | TGAAACACCTTGAAG[A/G]TGGATAGGATTAGAA | 1161 |
rs185979431 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939241 | TATATATTTCCAGCT[A/T]GTTTATTATTATATA | 1161 |
rs185983653 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919880 | ACAGTAATTATGGGA[A/G]GAAAGGTGTATACGC | 1161 |
rs186050887 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884368 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 1161 |
rs186066384 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915619 | TTGGAGGCTCTAGGA[A/G]AGAATACTTTCTCCA | 1161 |
rs186081695 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945869 | TTCAGCGCCTCGGCT[A/G]TCTTCTTTCTTGGTG | 1161 |
rs186129584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881165 | ATCAGCTCAGAGACT[A/G]CAGAACAGTGGATAT | 1161 |
rs186133263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881355 | TCAGATCTCCAGCTG[C/T]GTGCTGGGAGAACCA | 1161 |
rs186160679 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940207 | AATACTACTATAAAA[A/C]CTAAACAAAATGCAG | 1161 |
rs186198610 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888561 | TCAAGAAAGAGATAT[A/T]GAAAGCAGCAACATT | 1161 |
rs186227183 | snp | A/C | | | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60903168 | ATATTCTATCTTTTC[A/C]TTGTTTAGAATTAGA | 1161 |
rs186275978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884088 | GAATAACTTTGATTA[C/G]ACAATTCTGATATTT | 1161 |
rs186285155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898003 | ATCAGTAGTCCTCAG[C/T]CTTTTATTTTTCTCT | 1161 |
rs186291062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902063 | GCACGTGGGAGGAAG[C/T]CATTAAATATTAGAA | 1161 |
rs186378848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888899 | ATTCATGTTTCATTA[C/T]TTGTTCCAATACTGT | 1161 |
rs186381825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925410 | ACTTTGACTGGTTAG[C/G]TCTTTGGAAAGATAT | 1161 |
rs186398817 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884711 | TCATGATCACATTCA[G/T]GTTCTGCCTATATTC | 1161 |
rs186408782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920263 | TCTTCCAATAAATTT[C/T]GCTTAAGATAAGCAG | 1161 |