SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs186565039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874756 | TAGGCTCACAATAAA[A/G]TTATGAAATATATCA | 1161 |
rs186606779 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907513 | GCCCGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 1161 |
rs186700700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909706 | CGCCTGTAATCCCAA[C/T]ACTTTGAGAGGCCGA | 1161 |
rs186718803 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927765 | TGTCCTTGAATAGAA[A/G]GTGTTACACTGAGCC | 1161 |
rs186750690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886041 | TTTATATTTCCAACT[G/T]AAAGAACTATATGTA | 1161 |
rs186761116 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921733 | ATGAATCTTACACTA[A/T]GTGGTACTAAAAACT | 1161 |
rs186766096 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876452 | TACCTGGGGAATTCC[C/T]ACATGGACTTCCACA | 1161 |
rs186768425 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903919 | TAGTAGTAAGAGACC[A/T]CTATTATTACATTTA | 1161 |
rs186773800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892028 | CTGCACATTTCTGTA[A/C]ATTCTTACTCTTCAG | 1161 |
rs186827909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913344 | GTGTGTCGAGGAATT[C/T]ATCCATTTCTTCTAG | 1161 |
rs186837413 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895797 | GATGGCCTTATTCAC[A/G]TTTGTTTCTCAGGAC | 1161 |
rs186845372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931233 | TGATTATAAGATTAA[C/T]AGAAGAGTAATTTGC | 1161 |
rs186910139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879490 | AGTCTCCCATTATTA[C/T]TGTGTGGGAGTCTAA | 1161 |
rs186930351 | snp | A/C | 0.000117285 | 0.00765695 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945431 | CAGTGATTGCGAGGT[A/C]AGTAAAGGAGGGAAA | 1161 |
rs187054324 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898120 | AAGGGTGGGTTGTCC[C/T]GAGTTGAGAATTACT | 1161 |
rs187089092 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935867 | ATATGTTAAACCATC[A/C]CTGCATTCCTGGTAT | 1161 |
rs187122114 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930968 | AAAAAAATTAGCCAG[G/T]TGTGGTGGGGCATGC | 1161 |
rs187123383 | snp | A/G | | | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60873895 | ATTCCCTGCCAGGAT[A/G]TTTTCTGCTTGAATT | 1161 |
rs187210229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919228 | AAACGATAGGTTGTT[C/T]GAGATTTGCTTCAAC | 1161 |
rs187228731 | snp | C/T | 0.132409 | 0.220618 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894070 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 1161 |
rs187254963 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60916047 | AATTCTTCTCTCCAG[G/T]ACCATGTGACTGGGG | 1161 |
rs187431738 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912184 | AAATTACCTTGGGCA[A/G]TATGGCCATTTTCAC | 1161 |
rs187434424 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878502 | AATCCATCTGGTCCT[A/G]GACTTTTTTTGGTTG | 1161 |
rs187437964 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938644 | CAGGCGTGAGCCACA[G/T]CGCCCGGCTGAATTT | 1161 |
rs187463020 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878716 | GGATTGGTGGTGATA[A/T]CCCCTTTATCATTTT | 1161 |
rs187560776 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60922237 | GCAAATTTCTAAAAA[C/T]TGATTTGCAAACACT | 1161 |
rs187579321 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942141 | ATATAAAATAGAATA[C/G]TAAATAATGTTCAAA | 1161 |
rs187581509 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896016 | TTGAGACGGAGTTTT[C/T]GCTCTTATTGCCCAG | 1161 |
rs187589876 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932196 | GCAATAATACTATAA[A/C]GGGAAAGAGAGGTGG | 1161 |
rs187635667 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905014 | CATAGGAATGTAATA[A/C]CCCAAAAAACCTTGA | 1161 |
rs187684387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926575 | AATGCCCTACTTAGT[C/T]ATTTTAAAAAATATT | 1161 |
rs187689807 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881852 | GCTCATGCTCAGTGC[A/G]CTGCACCCACTGTCC | 1161 |
rs187695425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882132 | AGGCGTGAGCCACTG[C/T]GCCCGGCTTAGAAAC | 1161 |
rs187709274 | snp | A/C | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946414 | ATTCTGTGATTTATC[A/C]CTCAATTAATTTATT | 1161 |
rs187711318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900137 | CTTTGCTCAAGAATC[C/T]ATTTGGTATGATTTG | 1161 |
rs187722199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917339 | TTTAGTTGCAGCAAA[A/G]CATTTGTGTTGAAAA | 1161 |
rs187783125 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908900 | CCTTTGACCTCTTAT[C/T]GAAAATCCATCTTTT | 1161 |
rs187832884 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942979 | GATGGAAATATTTTT[A/T]AAAAAATTTTAGGCT | 1161 |
rs187833523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879896 | GTTATGTGTGAATTT[C/G]ATCCTGTCATGATGA | 1161 |
rs187845686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940868 | AGAGTATTCAAAATG[A/T]CCAGGATGCAAATCC | 1161 |
rs187865195 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914243 | GTCTCCTTGTAGGTC[C/T]GTATGGACTTGCTTA | 1161 |
rs187924809 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936933 | AGATCTGGGACTCAA[C/G]GGCTGCTCTGCAGAT | 1161 |
rs187997475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899563 | TATTATGTGGCTTCA[A/G]TTAAAAATTTTCAAT | 1161 |
rs188063271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906494 | AGTACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 1161 |
rs188072519 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943780 | CATTCTAGATATGCA[G/T]ACTGAGGAAATCAGT | 1161 |
rs188074865 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924196 | TTTCCCATTGCTCTT[G/T]GTTGTGATGTGATAT | 1161 |
rs188088729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923224 | AATTATTCTATTCAA[A/G]AACTTTGCAAAAATA | 1161 |
rs188154053 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873440 | AGCACTTTGAGAGGC[C/T]GAGGCGGGTGGATCA | 1161 |
rs188348629 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891442 | AGTGTAATTTGGCTA[C/T]TCTTTCTAAAAGGGC | 1161 |
rs188356916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927451 | CAATAAAGCGGAAAA[A/T]CACTGTAGCAAGAGT | 1161 |
rs188501876 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886970 | ACACATAGTTATTAA[G/T]GACATGAAAAAAGGC | 1161 |
rs188509939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912865 | CATGCGGTTTTTGTC[A/T]TTGGTTCTGTTTATG | 1161 |
rs188510958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880795 | AGGTTTTTAACTTCT[C/T]TGCCATGGGTTCAAA | 1161 |
rs188519362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915386 | AGGAGAGGGAAGATC[A/G]TATCAATTCAAACAT | 1161 |
rs188527677 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897566 | AATTATTAAACCATA[A/G]GCATATCTGATAAGA | 1161 |
rs188614233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937163 | GTGGATACCAGCACC[A/G]GCAACCGTAGAGGCA | 1161 |
rs188647416 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909234 | ATGCAGACAAAAATG[C/T]CCTATTCTGAAAAAA | 1161 |
rs188647569 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946724 | TTGTTTTTGACAAAT[A/G]AGTAGAGTAACCTCA | 1161 |
rs188669503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875676 | ATTATTTTAGATTTA[C/T]TGCCTTTTATAACTT | 1161 |
rs188775861 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895241 | GTGTGTATGTGTATG[C/T]ATATATATACATAAA | 1161 |
rs188824309 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934273 | ATTTTTTGATTATGG[C/T]CATTCTTGCAGGACT | 1161 |
rs188870195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917516 | ACTTAGTGTAGAAAA[C/T]GTAGAAGGTAAGGCA | 1161 |
rs188955963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890384 | AAACCATCTGCTCCA[C/T]TGGTGATATGAAAAG | 1161 |
rs188978061 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937780 | GCCTGCAGCGGCAAT[C/T]CACTTCCTTCAAAGG | 1161 |
rs188982159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917873 | TCAATCAAAGATAAA[C/T]CCAATTTTCTACTTT | 1161 |
rs189032037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925392 | GTTCTGTACTGGGGG[C/T]GCACTTTGACTGGTT | 1161 |
rs189051346 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882671 | GGATTACAGGCGTGA[C/G]CCACCACTCCTGGGC | 1161 |
rs189059509 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877623 | TTCCTAGGTATTTTA[A/G]TCTCTTTGAAGCAAT | 1161 |
rs189069446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901358 | CTTTCATTTAATGTT[G/T]TAATTTCTGTGGCTT | 1161 |
rs189088204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898051 | CATTGAGAACAGTGG[C/T]TCAGTAGAACAGTGA | 1161 |
rs189119043 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934909 | GGGTTCTCCACTCTG[A/T]TCCGTTGGTCTATAT | 1161 |
rs189122330 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896427 | GTGTTAGCCAGGATG[G/T]TCTTGATCTCCTGAC | 1161 |
rs189132538 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880684 | CTTGAACATTCATCA[C/T]GTAGTTCTCGTGCCA | 1161 |
rs189169640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928677 | AGCTTGGAAATGTTT[A/G]TTTGACAACATTTGG | 1161 |
rs189175875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884251 | TTGGGAGGCCGAGGC[A/G]GGTGGATCATGAGGT | 1161 |
rs189245747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883555 | ATGAGTTTAGAGAAG[A/G]AATAGAACCAAACTT | 1161 |
rs189249793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918584 | CTCCCACTGTGTGAT[A/G]TAGAGACATACCTCC | 1161 |
rs189387620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915795 | TGATTACATTGGGCC[C/G]ACTAGGATAATTCAG | 1161 |
rs189406100 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905953 | GTGGGGAATGGTCCT[C/G]TTGTGCACTAAGCCA | 1161 |
rs189475809 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919557 | CAGCTGCAAAAATAC[A/T]AGAACTATAGTGCCT | 1161 |
rs189482050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902175 | TTTAAAAATTAGCAC[G/T]GTGTTATACATTTGT | 1161 |
rs189519827 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901895 | TGATCCTGCTTTCTT[C/T]TCCTATATTACACCT | 1161 |
rs189673886 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887384 | CACATAAAGTAACAA[A/C]ACATTATTTCTTAAG | 1161 |
rs189705435 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945974 | GTAGGTCCATATCCC[A/C]ACAAGGCTCGCTGAT | 1161 |
rs189707531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926166 | ACTACAGTTTTTGGC[A/T]CTACATTCACTGAGT | 1161 |
rs189774423 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889886 | GGATATACCTTCTTA[A/T]TGACTAATAAAAAGA | 1161 |
rs189786511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875313 | AAAACATGCAAAATA[C/T]GTCAGAAATGGTAAC | 1161 |
rs189788446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908677 | GTGATGCTGCAAGTG[A/G]TACCAAGAAGCAGAG | 1161 |
rs189856814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930023 | TGATACTTTCATTCA[C/T]TGACATTAGTACAAG | 1161 |
rs189894368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893268 | CATCCAGCTGAGGAA[A/T]CATATTTAATTCCTG | 1161 |
rs189921460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929417 | CCCAGGCAACATAGC[C/G]AGACCCCATCTCTAC | 1161 |
rs189939729 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878041 | GTTATTTTGAGATAC[A/G]TCCCATCAATACCTA | 1161 |
rs189942713 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911791 | TAAGGAAGGGATCCA[G/T]TTTCAGCTTTCTACA | 1161 |
rs189947183 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893653 | GGGGATCTGAGAAGA[C/G]AGAGTAACAGACGCT | 1161 |
rs190076110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888729 | CAGTCCAAAAGACTT[A/C]TTTTCCCCCTTGAAT | 1161 |
rs190080881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874801 | ACATTATTTTGGAAG[A/C]AAATGTATAACTGTT | 1161 |
rs190161593 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911438 | CCTACTTTTTGATGG[G/T]TTTTTTTTTTTCTTG | 1161 |
rs190195125 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876834 | ATTCTGTAGGTTGCT[A/T]GTTCACTCTGATGGT | 1161 |
rs190215598 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910195 | TATCATAAATCAAAT[A/T]AATGTCATCAACGGG | 1161 |
rs190287955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898940 | ATAGTTTACATGTTT[C/T]ATAAGGTTTTTTAAA | 1161 |
rs190294834 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60873914 | TCTGCTTGAATTAAT[A/G]AGGCAGGATTTGGTC | 1161 |
rs190296196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936426 | TTGTTGGTTAATCTA[A/G]CTAATGGTCTATCAA | 1161 |
rs190300008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917001 | TGAAATAGGAATACA[C/G]AAAATAGTGCTATAA | 1161 |
rs190313017 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907387 | TGAGATGGAGTCGCT[C/G]TGTTGCCCAGGCTGG | 1161 |
rs190426591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902698 | GGGGTATTTCAAACA[C/T]ATGGTATTTTATTGT | 1161 |
rs190439270 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895368 | ACATGCATTTAGCTA[A/C]CTCATGGCAGTAGCA | 1161 |
rs190441358 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939362 | TGGTTTTTGATTAAC[A/G]TTCTTTCCTAATTTT | 1161 |
rs190447513 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879110 | CATCTTTATTTCTGC[C/T]TTCATTTCGTTATGT | 1161 |
rs190449216 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920078 | AGAGTTAGCCATTAT[C/T]CAAAGCTGAGGAGTT | 1161 |
rs190548560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938667 | CTGAATTTGTTAAAG[C/T]TTGCTTAGTGGCCAA | 1161 |
rs190594921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881682 | GGATATAATCTCCTG[A/G]TGTGCTGTTTGCTAA | 1161 |
rs190683586 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946656 | CTGAGTTTTTTTAAA[C/T]TGAAATATAATTTAC | 1161 |
rs190790649 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885184 | AACCTGGCTAATTTT[A/G]TCTATTTTTTGTAGA | 1161 |
rs190794971 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920411 | TTAAGTTTAAATTTT[A/G]AAATAGGATATTTTA | 1161 |
rs190933905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881246 | CAGAGGTGCACCTGG[C/G]TCTGTGAGGTGTCAG | 1161 |
rs191031496 | snp | A/C | 0.0052226 | 0.0508333 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903566 | TAGTCATGTCACTTA[A/C]AAAGAATACACTGTT | 1161 |
rs191063390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940703 | TTGAATGGCATACAC[C/G]TGGGGAAGATCTGAA | 1161 |
rs191137111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941653 | GCTGAAAACTAAAGA[C/T]GAAGTCTTCAAAGCA | 1161 |
rs191138266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876763 | TTGTTTGAGTCCATT[A/G]TAGGTTCTGGATATT | 1161 |
rs191143378 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60921841 | TAATGAAAATTGATA[A/C]TGAAGTTGCTTTGGG | 1161 |
rs191162707 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909846 | GTAGTCCCAGATACT[C/T]GGGAGGCTGAGGCAG | 1161 |
rs191167022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892250 | TATACAGTAGCTTTA[C/T]CTTCAATGGCATCTG | 1161 |
rs191178956 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928382 | CTTGTTAGGTAGGTA[C/G]TATTGTTCCCATTGT | 1161 |
rs191299436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879684 | CAGAGACTAGGATTA[A/C]AACCTCTGCCTTTTT | 1161 |
rs191305913 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913560 | TCCTGGATTCATTGA[G/T]TTTTTGAAGGGTTTT | 1161 |
rs191314637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895970 | TACAACTTAATGTCA[C/T]ATTAATATTTCTTTT | 1161 |
rs191320538 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931276 | AGCTAATATTTGGCT[A/G]AGCCGCATTTGAACT | 1161 |
rs191350108 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881796 | GGGAATTCCCTGACC[C/T]CTTGTGCTTCCCAGG | 1161 |
rs191356591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908135 | GTCTTGTTCTATGTA[A/C]TCCTTTCAAATGCCA | 1161 |
rs191451858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931194 | GTAGTCCCAGGAGTG[G/T]TGATTATTATTAAAT | 1161 |
rs191579796 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888930 | CCTTTATAGCAAAAG[C/G]GACCAGTTAAAAATC | 1161 |
rs191590002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925730 | AGTTTGGTTGTAAGT[C/G]TTAATCTGGTTTTTC | 1161 |
rs191603480 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890523 | ATAGATCATCCACAC[A/T]TACATAAACCAACAT | 1161 |
rs191606189 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926973 | CTGACATTAACTATG[A/C]GATACTTTTTGCTGA | 1161 |
rs191686380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913145 | TCTTTTTCTATTGAT[C/T]GGAATAGTTTCAGAA | 1161 |
rs191748549 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884403 | ATGGCGTGAACCCAG[A/G]AGGCGGAGCTTGCAG | 1161 |
rs191873084 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891574 | ACCAAGAATTTTTTT[G/T]GGGGCTAATACCCCC | 1161 |
rs191877519 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876256 | GGTATATATGTGCCA[A/C]ATTTTCTTAATCCAG | 1161 |
rs191886629 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938011 | TTAATATGTATGCGT[A/G]TGTGTGTGTGTGTAT | 1161 |
rs191887512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909048 | GGATCTAAAGCTGGA[A/G]AATTGAATGCCAGAT | 1161 |
rs191890880 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917903 | TAGATTACTAGATCA[C/T]AGTATTTTTCACAAA | 1161 |
rs191891344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875677 | TTATTTTAGATTTAT[C/T]GCCTTTTATAACTTA | 1161 |
rs191894011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936096 | AACAGTGTCAATAGG[A/G]TTGATACAAATTCTT | 1161 |
rs191966479 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933253 | AGACGGAGTCTCACT[C/G]TGTCACCCAGGCTGG | 1161 |
rs192041599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923009 | AACAATCCAAGCCCA[C/T]TCTAGGAACCAAAAG | 1161 |
rs192050332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914890 | TCATTCTATTAACAT[C/G]ATGAATTACATTAGT | 1161 |
rs192053818 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942418 | ATGTCCATCGACAAG[C/T]GACTAGATAAACTGT | 1161 |
rs192108400 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878572 | TTGGTCTATTCAGAG[A/T]TTCAACTTCTTCCTC | 1161 |
rs192121709 | snp | A/C/G | 0.0170531 | 0.0909808 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912650 | AGGAGTGGTGAGAGA[A/C/G]GGCATCCCTGTCTTG | 1161 |
rs192183306 | snp | G/T | 0.000164845 | 0.00907719 | missense | ERCC8 | GRCh38.p7 | 5:60899662 | TTTTTCCCATTATGT[G/T]GATCAAGAGTAATCA | 1161 |
rs192184415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882259 | CAGTAGAAAAAGTTA[C/T]GTGTTCCTAGTACAT | 1161 |
rs192205308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900700 | AAGGAAATGAAATCA[A/G]TATGAGGATTTAAGT | 1161 |
rs192208161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937013 | CTAAGGTTGGGGCTT[C/T]CTGAGAGCCAAACTG | 1161 |
rs192366219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888063 | TATGTCAATGTCTAC[A/G]GATATGCTGTTTGCT | 1161 |
rs192477228 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894219 | TCGATCTCCTGACCT[C/T]GTGATCTGCCTGCCT | 1161 |
rs192481093 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937469 | TGGGTGAGGCTTGCC[A/G]CTGCTGCTGTGGTAG | 1161 |
rs192492825 | snp | G/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930924 | TCAGCCTGGCCAACA[G/T]GGTGAAACCCCGTCT | 1161 |
rs192588740 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881954 | CTTCTGCATTGCTCA[C/T]GCTGGGAGCTGCAGA | 1161 |
rs192599681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917340 | TTAGTTGCAGCAAAG[C/T]ATTTGTGTTGAAAAC | 1161 |
rs192671793 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923293 | CTATATACATTGATT[A/G]AACTTAATAATTTGT | 1161 |
rs192678440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886451 | TCATGCGTGTAATCC[C/T]AGCACTTTGGGAGGC | 1161 |
rs192695896 | snp | C/T | 0.000148396 | 0.00861255 | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904843 | TATGATGACTATAAA[C/T]TGTTTCCTCAAAATT | 1161 |
rs192755738 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883402 | TTATTTCAGTTTTCT[C/T]TGCAACATCTCCTCC | 1161 |
rs192758544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909326 | AATGATATGGGCTCT[A/G]AAACTAAAGCAAATA | 1161 |
rs192837494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905055 | TCCTGTCATTTACAA[C/T]ATTCTTTTCCCTTCT | 1161 |
rs192894836 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906262 | GCTGGTCTCGAACTC[C/G]TGAGCTCAAGCAATC | 1161 |
rs192895225 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943399 | AGAAATAGCATAAAA[A/G]TTTGCTACTAGCTTT | 1161 |
rs192970383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901483 | CAGATCCATACTATC[C/T]TTCCTCAAAATTGCA | 1161 |
rs192972441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927511 | AAAGATGCCTCATCT[G/T]CATTTCTCAAATATA | 1161 |
rs193047363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887036 | AAGTTGAATGTCCAA[C/T]CATGATATGAACTAT | 1161 |
rs193130102 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914403 | TATCAGAGACCAGGA[C/T]TGCAACCCCTGCTTT | 1161 |
rs193149884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879919 | CATGATGACATTAGC[C/T]GGTTATTTTGCTCGT | 1161 |
rs193279626 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896049 | TGCAGTGCAATGGCA[A/T]GCTCTCGGCTCACCG | 1161 |
rs193282355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932517 | CTAATGAGCTTCCCT[A/G]ATAGACATTTCACAT | 1161 |
rs199546245 | in-del | -/A | 0.457737 | 0.139088 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938349 | ATAGCTACCTTTTTG[-/A]ATTTTTTTTTTTTTT | 1161 |
rs199547728 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938008 | GAGTTAATATGTATG[C/T]GTGTGTGTGTGTGTG | 1161 |
rs199574585 | in-del | -/ATT | 0.0275645 | 0.114116 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908705 | GAGAAAAGTCATGAC[-/ATT]ATAAAAAAAGGCTGA | 1161 |
rs199590588 | snp | C/T | 0.000214212 | 0.010347 | missense | ERCC8 | GRCh38.p7 | 5:60887492 | ACCCAAGCCAGAATG[C/T]TGCAGTCTCTGCTAC | 1161 |
rs199591129 | snp | C/G/T | 2.01161e-05 | 0.00317138 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945222 | CCCTACTGCGGGTCC[C/G/T]GCTGCTGGCAGCGCT | 1161 |
rs199605141 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876125 | TGAGTGAGAACTTGG[C/T]GGTGTTTGGGTTTTT | 1161 |
rs199607120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899765 | TTGACATATGTAGCT[A/G]GGACAATGACTGTAC | 1161 |
rs199754807 | snp | C/G | 9.91309e-05 | 0.00703958 | upstream-variant-2KB, stop-gained | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945369 | CTACATCCCGCAGTA[C/G]AAGAACTGGAGAGGT | 1161 |
rs199799664 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877801 | TTTTCTAGATATACA[A/G]TCATGTCATCTGCAA | 1161 |
rs199805243 | snp | C/T | 9.91211e-05 | 0.00703923 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60890997 | AATGGTGCTACCATA[C/T]GGTACAAAAACAAAT | 1161 |
rs199823594 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906734 | ACTCTGTCTCAAAAA[A/T]AAATAAATAAATAAA | 1161 |
rs199847260 | snp | C/T | 3.29995e-05 | 0.00406185 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928912 | TTAATTCCACCGCCG[C/T]GGATTCTTTCAACAT | 1161 |
rs199871570 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882603 | CATATTGGCTAGGCT[C/G]GTCTTGAACTCCAGA | 1161 |
rs199887744 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915035 | TGTAAGAGACACTGG[C/T]TTGTAATTTTCCATA | 1161 |
rs199904705 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878234 | GCCCACTTGTTCATG[C/G]TGGATAAGCTTTTTG | 1161 |
rs199955793 | in-del | -/A | 0.0228947 | 0.104514 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927038 | TAGACAAGAAAACTT[-/A]AGTATTAAAGATGAA | 1161 |
rs199968351 | snp | C/G/T | 4.94355e-05 | 0.00497149 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945011 | AAAACCCCAGCATAT[C/G/T]GTGTCCTCACACCGG | 1161 |
rs200096138 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943875 | GGAAGTGACACTGGC[-/A]AAAAAAAACACATTA | 1161 |
rs200182680 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942546 | AAAGAAGCCAGACAA[A/G]AAAGATTCCATTTAT | 1161 |
rs200202569 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931113 | AAAGCAAGCAAGACT[C/T]CGTCTCAAAAAAAAA | 1161 |
rs200205429 | snp | C/T | 9.92556e-05 | 0.007044 | synonymous-codon, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922137 | TACAATCACACCATC[C/T]GAACCACCTGATAAC | 1161 |
rs200217057 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908583 | TATATATATATATAT[-/A]TTTTTTTTTTAAATA | 1161 |
rs200242670 | in-del | -/TATATATATATATTTTAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938074 | ATATATATATATATA[-/TATATATATATATTTTAT]TTTTTTTTTTTTTAG | 1161 |
rs200293326 | snp | A/G | 4.96339e-05 | 0.00498142 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899762 | ACATTGACATATGTA[A/G]CTAGGACAATGACTG | 1161 |
rs200299226 | snp | A/G | 0.0281818 | 0.115311 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945223 | CCTACTGCGGGTCCC[A/G]CTGCTGGCAGCGCTG | 1161 |
rs200329776 | in-del | -/T | 0.491732 | 0.0637633 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884524 | ATATGTGTGTATGTG[-/T]TTTTTTTTTTTTTGT | 1161 |
rs200414363 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891566 | CTACCCCACCAAGAA[-/T]TTTTTTTTGGGGCTA | 1161 |
rs200513212 | snp | A/C | 0.00299557 | 0.0385851 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60887476 | TTCATATAAGGATGG[A/C]ACCCAAGCCAGAATG | 1161 |
rs200624611 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878199 | TGTATGTTGAACTAG[A/C]CTTGCATCCCAGGGA | 1161 |
rs200733672 | snp | G/T | | | missense | ERCC8 | GRCh38.p7 | 5:60891002 | TGCTACCATATGGTA[G/T]AAAAACAAATTCTGA | 1161 |
rs200839942 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894943 | TGGGAGGCCGAGGCA[A/G]GCGGATCACAAGATC | 1161 |
rs200846878 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944966 | TCCGAAGGCGAAGAG[A/G]GTCCTCCAAACCCGT | 1161 |
rs200881652 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904630 | ATATATAGTGTGTGT[A/G]TGTGTATATATATAT | 1161 |
rs200938280 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911660 | TTAGACATGAAGTCC[C/T]TGCCCATACCTATGT | 1161 |
rs200975738 | in-del | -/TTTCT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875890 | TTAATTTATTTATTT[-/TTTCT]TTTTTTTATTATACT | 1161 |
rs200980327 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911436 | TGCCTACTTTTTGAT[-/G]GGTTTTTTTTTTTCT | 1161 |
rs201096272 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931405 | TCAAACTCCTGGGCT[C/T]AAGGGATCCTCTTGC | 1161 |
rs201103085 | snp | A/G | 1.67964e-05 | 0.00289792 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945433 | GTGATTGCGAGGTCA[A/G]TAAAGGAGGGAAAAG | 1161 |
rs201126529 | snp | A/G | 0.000999417 | 0.0223318 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903733 | TGTAAAAACAGAACC[A/G]GTTTAAGATAATTTT | 1161 |
rs201161101 | in-del | -/ACAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883003 | CACACACACACACAC[-/ACAT]GTCTGTAGGTGGATA | 1161 |
rs201208798 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908965 | CTATATGTAGACTCT[A/C]ATATGACTTTTAAAA | 1161 |
rs201288445 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898795 | CTAGTGTTTTCCATT[A/G]AAAAAAAAAACAGGG | 1161 |
rs201295435 | snp | A/C/T | 1.65236e-05 | 0.00287429 | upstream-variant-2KB, synonymous-codon | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945360 | CAAATACTACTACAT[A/C/T]CCGCAGTACAAGAAC | 1161 |
rs201327177 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944922 | AGCCAAAAAGTAAGG[C/T]TTTCTTTACCTCCGT | 1161 |
rs201423526 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881814 | TGTGCTTCCCAGGTG[A/G]GGCGATGCCTCACCC | 1161 |
rs201464610 | snp | A/C/T | 4.95138e-05 | 0.00497543 | splice-acceptor-variant | ERCC8 | GRCh38.p7 | 5:60899728 | ACTCTACTGTCAGCA[A/C/T]TGAGAAGAAATAAAT | 1161 |
rs201477710 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878233 | AGCCCACTTGTTCAT[C/G]GTGGATAAGCTTTTT | 1161 |
rs201507355 | in-del | -/A | 0.228842 | 0.249103 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878733 | CCTTTATCATTTTTT[-/A]TTGCGTCTATTTGAT | 1161 |
rs201535238 | snp | C/T | 0.000233992 | 0.0108139 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922183 | AAGTTCACATTAATT[C/T]ATCATTTTATTTATT | 1161 |
rs201579764 | snp | C/T | 0.000366758 | 0.0135368 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902400 | TTTTCAAAATGCTTA[C/T]TATTAATTACTAACT | 1161 |
rs201611698 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905290 | AAATCATACATTTCA[G/T]TTATCTATGACCACA | 1161 |
rs201642761 | snp | C/T | 9.91867e-05 | 0.00704155 | missense | ERCC8 | GRCh38.p7 | 5:60891019 | AAAACAAATTCTGAA[C/T]TGCAGCCACAGGAGA | 1161 |
rs201681903 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904632 | ATATAGTGTGTGTGT[A/G]TGTATATATATATAT | 1161 |
rs201758975 | in-del | -/TATATATATATATATTTTAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938072 | ATATATATATATATA[-/TATATATATATATATTTTAT]TTTTTTTTTTTTTAG | 1161 |
rs201833381 | snp | A/G | 0.000119553 | 0.0077306 | intron-variant, missense | ERCC8 | GRCh38.p7 | 5:60903626 | CTCAAAGTAGTTGCC[A/G]TTTGAAATAAAATAA | 1161 |
rs201840328 | snp | C/G | 1.65567e-05 | 0.00287716 | missense | ERCC8 | GRCh38.p7 | 5:60903665 | TGTAGAATGTGAGAA[C/G]AGGATCCAGACTTCA | 1161 |
rs201915477 | snp | A/C | 0.000280114 | 0.0118313 | missense | ERCC8 | GRCh38.p7 | 5:60887445 | TAATATTTACCTCAT[A/C]ATCATCAGGAACTGG | 1161 |
rs201951290 | snp | A/C | 1.6519e-05 | 0.00287388 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898405 | AGCAGTGTTTGCTGC[A/C]ATGAAAAACATAGTT | 1161 |
rs202142977 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885618 | TATGCTAAAGTTAAT[G/T]AAGCCACAATAAACC | 1161 |
rs202170789 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881153 | GTTTGCCTGGCTATC[A/T]GCTCAGAGACTGCAG | 1161 |
rs202185871 | snp | A/G | 4.94189e-05 | 0.00497062 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944957 | ACTCTGCTCTCCGAA[A/G]GCGAAGAGGGTCCTC | 1161 |
rs202244423 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934688 | CTTCTAGAATTTTTA[A/T]GGCTTCAGGTCTTAG | 1161 |
rs281875221 | snp | G/T | | | missense | ERCC8 | GRCh38.p7 | 5:60887479 | CAACATTCTGGCTTG[G/T]GTTCCATCCTTATAT | 1161 |
rs281875222 | snp | A/G | | | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904795 | AAGCACTGTTTGGTA[A/G]CAGGTTTGTAAGTGT | 1161 |
rs281875223 | snp | C/G | | | missense | ERCC8 | GRCh38.p7 | 5:60902477 | ATTAGCAGTTTCCTG[C/G]TCTCCACGTTATGAC | 1161 |
rs281875224 | snp | C/T | | | missense | ERCC8 | GRCh38.p7 | 5:60902454 | GTTATGACTATATCT[C/T]GGCAACAGCAAGGTA | 1161 |
rs281875225 | snp | A/G | 1.65165e-05 | 0.00287367 | ERCC8 | 5 | allele_origin=G(unknown)/A(germline) | 5:60898322 | TCACTGTTGGTACAG[A/G]TAATCGAATGAGGCT | 1161 |
rs367583920 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879268 | TTCTTTTACATTTGC[C/T]GAGGAGAGCTTTACT | 1161 |
rs367600615 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910575 | TTCTAAAGTTCTCTG[C/T]GTATTCGGAATAGTC | 1161 |
rs367623962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922781 | AACAACTGTCAACAA[A/G]GCAGGCATGGTTCCT | 1161 |
rs367632666 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, missense, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918274 | ACTTACTTGTAATGT[A/G]TTTGTATCCCATACT | 1161 |
rs367633626 | in-del | -/AT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909295 | CCACAAAGGACTCTT[-/AT]GACATGGACCCTTCA | 1161 |
rs367680344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939528 | TTTGAGACAGAGTCT[C/T]GCTCTGTCACCCAGG | 1161 |
rs367700106 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913298 | CTATTCAGAGATTCA[A/G]CTTCTTCCTGGTTTA | 1161 |
rs367797045 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892198 | CATCTGATGACGATT[C/T]GGATTGGTGCAATAA | 1161 |
rs367797260 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894276 | GGCGTGAGCCACTGC[A/G]CCCGGCTGGGAATTT | 1161 |
rs367814734 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927744 | ATAAGTGAGTGCCCC[C/G]CCAGCTGTCCTTGAA | 1161 |
rs367835814 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917370 | CTGGTAGAACATAGG[A/G]TTGAAGGAACAAGGG | 1161 |
rs367874889 | snp | A/C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918362 | TGTACAGTCTCCACA[A/C/T]TGTATCTGTGAACAT | 1161 |
rs367883713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938960 | GAATTTTGTAAAGTA[C/T]TTTAAAATATTTTAA | 1161 |
rs367886044 | snp | C/T | | | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904867 | CAAAATTAAATACAT[C/T]TGCAGTCTGGTAATC | 1161 |
rs367990538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913899 | CCCACGCAGTTGTGT[A/G]GTTTTGAGTTAGTTT | 1161 |
rs368000623 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889442 | TCCTGCACAGCTGGG[A/C]CTACAGGCATATACC | 1161 |
rs368060722 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877869 | ACCCTTTATTTCCTT[C/T]TCCTGCCTGATTGCC | 1161 |
rs368069191 | snp | A/G | 3.32254e-05 | 0.00407573 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945047 | GCACTGGACGTCGCC[A/G]TGACAGAGCTCAGGG | 1161 |
rs368075257 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934067 | GTGAGTATCTTTTTT[A/G]TATAATGACTTCTCT | 1161 |
rs368224524 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937812 | TCTGTGGATCCTCTC[C/T]GCTTTCCTGGAGCGT | 1161 |
rs368226773 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882742 | TCTAGCCACGGTACA[C/T]TTATTTGCAACAGTT | 1161 |
rs368261057 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877962 | GCCTGTTTTCAAAGG[C/G]AATGCTTCCAGTTTT | 1161 |
rs368266145 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893752 | GGGCAGTCTCCACGA[C/G]GGGGCGGGGCTTCTC | 1161 |
rs368273837 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60898360 | AAGTCCATCACTTGT[A/G]AAACATAAGCCATTA | 1161 |
rs368308377 | snp | A/T | 0.000290242 | 0.0120431 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903578 | TTACAAAGAATACAC[A/T]GTTAGTAACGTTTCT | 1161 |
rs368324158 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898541 | ACTTAACCAACCCTT[A/C]AGATTATTTGAATAG | 1161 |
rs368423039 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879722 | CCATTTGCTTGGTAG[A/C]TCTTCCTCCATCCCT | 1161 |
rs368446242 | snp | C/G | 1.71457e-05 | 0.0029279 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945293 | TCCGCGCCTTGTGGA[C/G]ATCGCTGTCAAGGGA | 1161 |
rs368456106 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933340 | TCTCCTGCCTCAGCC[A/C]CCTGAGTAGCTGGGA | 1161 |
rs368459785 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911575 | AGTTTCTTTTGCTGT[A/G]CAGAAGCTCTTTAGT | 1161 |
rs368665460 | snp | G/T | 0.000153988 | 0.00877328 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874565 | GTTGAAAAAAACACA[G/T]TCTCATTTAAAAAGT | 1161 |
rs368676801 | snp | C/G | 1.67725e-05 | 0.00289585 | missense | ERCC8 | GRCh38.p7 | 5:60874647 | TGCTGCTCCAGGCAT[C/G]TTCAAAGGCCGGATT | 1161 |
rs368693328 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884538 | GTTTTTTTTTTTTTT[-/G]TTTTCTAGTGTGGTA | 1161 |
rs368737893 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900844 | CTCTCCTCTTATCTG[A/G]TGAAAACCAAGTTAA | 1161 |
rs368746106 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926888 | TGTCAGATGTTTTGA[C/G]TCTGTTAAAATGGCT | 1161 |
rs368763930 | in-del | -/AAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934071 | GTATCTTTTTTGTAT[-/AAT]GACTTCTCTTCTACT | 1161 |
rs368795383 | in-del | -/GTT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910083 | ACTAGGCTATTAGTA[-/GTT]AAGCTTTTGGGGTAA | 1161 |
rs368846360 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927985 | AATTCTGGGGGAAAT[G/T]CTAAACATACCATAA | 1161 |
rs368874320 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876244 | ATAGTATTCCATGGT[A/G/T]TATATGTGCCACATT | 1161 |
rs368908218 | in-del | -/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933216 | TTTTTCCTTTTTTTT[-/C]TTTTTTTTTTTTTTT | 1161 |
rs368908498 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914520 | ATGAGGATGGGCACA[A/G]TGGCTCATGCTTGTA | 1161 |
rs368967813 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906549 | GCCTGGCCAACATGG[G/T]GAAACTCCGTCTCTA | 1161 |
rs369027137 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895448 | ACTCATCTTTTTTTT[-/T]GCCCCTTATGAATAA | 1161 |
rs369049995 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880536 | TCTTTTCACATAGTC[C/T]CATATTTCTTGGAGG | 1161 |
rs369059194 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878102 | TTGAATTTTGTCAAA[C/G]GCCTTTTCTGCATCT | 1161 |
rs369063260 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894130 | GCTGGGACTACAGGC[A/G]ACCGCCACCACGCCC | 1161 |
rs369091328 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941320 | AACAGATTGGAGATG[A/G]CAGAGGAAAAAATCT | 1161 |
rs369119364 | snp | A/G | 1.65315e-05 | 0.00287498 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928853 | TGATTATACAAGTAT[A/G]ATAAACTTACTATCT | 1161 |
rs369140985 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928885 | CCTTCAACAGGTTCA[A/G]TGTCAAGGGTGTTAA | 1161 |
rs369216928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883998 | GGATATCAGGAGAAA[C/T]ACCCCTAAGGGATTA | 1161 |
rs369289856 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911551 | TAGGTTGCATGTTCA[C/T]TTAATGGTAGTTTCT | 1161 |
rs369317106 | snp | A/G | 1.66043e-05 | 0.00288129 | missense | ERCC8 | GRCh38.p7 | 5:60890908 | AAATTTGACTGAAAT[A/G]CACAGCAGTCAACAG | 1161 |
rs369322362 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878574 | GGTCTATTCAGAGAT[A/T]CAACTTCTTCCTCGT | 1161 |
rs369340696 | snp | C/G | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943361 | CTGATATGAATTTCA[C/G]TTACCACAGTTTATT | 1161 |
rs369365521 | snp | A/G | 0.000152135 | 0.00872033 | intron-variant, stop-gained | ERCC8 | GRCh38.p7 | 5:60903606 | TCTTTTTATTGAATC[A/G]TTTACTCAAAGTAGT | 1161 |
rs369398341 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899924 | AAGTGAGTAAATAGC[-/A]AAAAAAAAAAAGTAA | 1161 |
rs369472158 | snp | A/T | | | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919536 | GTGCCAGCTCTGGCA[A/T]TAAAACAGCTGCAAA | 1161 |
rs369506436 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60928175 | GTTATGACGAATTGT[A/C]AGTAGGAGAATATGT | 1161 |
rs369573212 | snp | A/G | 3.30382e-05 | 0.00406423 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898403 | TGAGCAGTGTTTGCT[A/G]CAATGAAAAACATAG | 1161 |
rs369678902 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914930 | GATGTTAAAACAACC[G/T]TTTTTGTCCACTCAT | 1161 |
rs369690794 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60880881 | GTCAATGTCATTCTC[C/T]ATCCAGTTTGTTCTG | 1161 |
rs369694150 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906059 | AAGATATCTCAAAAG[C/G]CCAATCTCAGGTTCT | 1161 |
rs369729956 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901321 | AGGTACTTTCCTGTA[A/G]ACACCGAAAATTGTT | 1161 |
rs369855334 | snp | A/G | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873417 | CAGTGGCTCAAGCTT[A/G]TAATTCCAGCACTTT | 1161 |
rs369930804 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931690 | CAAAACTTTTTTTTT[-/T]CATATTTTTCCATTG | 1161 |
rs369936433 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881560 | AAGCCTCAGCAATGG[C/T]GGGCGCCCCTCCCCC | 1161 |
rs369939385 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942620 | AGATTAGTAGTTTCT[A/T]GAGAAGGAAGAGGGT | 1161 |
rs369951599 | snp | C/G | 3.32071e-05 | 0.00407461 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922058 | TAAATACATACCTGC[C/G]AATGGAACACACTGC | 1161 |
rs369961779 | snp | A/G | 0.000153988 | 0.00877328 | missense | ERCC8 | GRCh38.p7 | 5:60899686 | GTAATCAAACATCCT[A/G]ATGCTCTTCTCACAT | 1161 |
rs369981959 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60916067 | TGTGACTGGGGAAAA[C/T]TGCTGTTCTTCAAAT | 1161 |
rs370117438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889700 | CTGGGATGAAATTTC[A/G]GCTGTGTCTCTAAGT | 1161 |
rs370121270 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886576 | GCGTGGTGGCGGGTA[C/T]CTGTAATCCCAACTA | 1161 |
rs370126311 | in-del | -/AATT | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946418 | TGTGATTTATCACTC[-/AATT]AATTTATTTTTGCCT | 1161 |
rs370152615 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60928735 | AATTAATAATGCCAG[A/G]TTCAAAAATGCTACA | 1161 |
rs370183705 | snp | G/T | 4.03218e-05 | 0.00448991 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891107 | GGATTAAAATAATAA[G/T]GTTACTCATCTCTGA | 1161 |
rs370251479 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877846 | ACTTCCTCTTTTCCT[A/G]ACTGAATACCCTTTA | 1161 |
rs370276324 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925507 | AGTATGCCATCTTCT[C/T]CCAGTTTGAGCTGCT | 1161 |
rs370282917 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902826 | CTCAATTACTGTAAT[A/G]AAACATATAAGATAA | 1161 |
rs370326323 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896759 | TAGATACGGACTTAA[C/T]AGAAAAAAATCCAAA | 1161 |
rs370342799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919894 | AAGAAAGGTGTATAC[C/G]CATGCTGGACAGCCA | 1161 |
rs370364064 | snp | A/C/G/T | 6.13119e-05 | 0.0055365 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945206 | GCGGCTGGAGCATTA[A/C/G/T]CCCTACTGCGGGTCC | 1161 |
rs370382611 | in-del | -/CACAG | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890132 | CTATATATCTTACAG[-/CACAG]TGTCAGGCACAAATT | 1161 |
rs370472176 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892337 | TCACCCAATAGCTCA[A/T]CAGATTCTCCAGTGG | 1161 |
rs370494217 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886161 | ATTAGGAGAATAAAC[C/G]TTGGTGGGAGAGAAA | 1161 |
rs370536140 | snp | A/C/T | 6.64931e-05 | 0.00576565 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945048 | CACTGGACGTCGCCA[A/C/T]GACAGAGCTCAGGGG | 1161 |
rs370547822 | snp | A/T | 5.112e-05 | 0.00505543 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904916 | ATAAGGTTTAAGTAT[A/T]AAAACAAAGCAATAA | 1161 |
rs370560478 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945593 | GCCTTGGCCCGGCCT[C/T]GTGCGTCCGCGGTCC | 1161 |
rs370563073 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896278 | CTGGAGTGCAATGGC[A/G]CGATCTCGGCTCACC | 1161 |
rs370564426 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879503 | TATTGTGTGGGAGTC[C/T]AAGTCTCTTTTTAGG | 1161 |
rs370569390 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911953 | TCCATAGGTCTATAT[A/C]TCTGTTTTGGTACCA | 1161 |
rs370618031 | in-del | -/CAGTT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905288 | TGAAATCATACATTT[-/CAGTT]ATCTATGACCACAAT | 1161 |
rs370650250 | snp | C/T | 0.000193981 | 0.00984647 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887388 | TAAAGTAACAAAACA[C/T]TATTTCTTAAGCTTT | 1161 |
rs370657735 | snp | A/G | 1.65214e-05 | 0.0028741 | stop-gained | ERCC8 | GRCh38.p7 | 5:60898317 | TCCAGAGCCTCATTC[A/G]ATTATCTGTACCAAC | 1161 |
rs370678226 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912561 | ACTTGACTTCCTCTT[C/T]TCCTAATTGAATACC | 1161 |
rs370761885 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930990 | GGGGCATGCCTATAA[A/T]CCCAGCTACTCAGGA | 1161 |
rs370885728 | in-del | -/GTAATCACAACAGT | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944293 | CTCTCCCGGACAAGT[-/GTAATCACAACAGT]TACCTAACTTGGCTC | 1161 |
rs370914049 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912059 | CTTTTGGCTTAGGAT[C/T]GTCTTGGTAATGCGG | 1161 |
rs370924240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933436 | GTTGGCCAGGCTGGT[C/T]TCAAACTCCTGACTG | 1161 |
rs370951941 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890527 | ATCATCCACACATAC[A/G]TAAACCAACATATAC | 1161 |
rs370962511 | snp | A/T | 0.0592355 | 0.161582 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877792 | ACAATGGGGTTTTCT[A/T]GATATACAGTCATGT | 1161 |
rs371103706 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917479 | TGAAACTGCTTTATA[A/G]TAAGATTAATTCTGG | 1161 |
rs371133123 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908398 | GGGTATGTATAGATC[A/G]ATTCCTGGATTATCT | 1161 |
rs371150465 | snp | G/T | 3.30109e-05 | 0.00406256 | missense | ERCC8 | GRCh38.p7 | 5:60898379 | CATAAGCCATTAACT[G/T]TCCCATTATGAGCAG | 1161 |
rs371152002 | in-del | -/TTTTAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938086 | ATATATATATATATA[-/TTTTAT]TTTTTTTTTTTTTAG | 1161 |
rs371181679 | snp | A/C/G | 9.89963e-05 | 0.00703491 | missense, synonymous-codon, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928911 | GTTAATTCCACCGCC[A/C/G]TGGATTCTTTCAACA | 1161 |
rs371296308 | snp | A/C | 0.00119087 | 0.0243724 | splice-donor-variant | ERCC8 | GRCh38.p7 | 5:60922052 | ACATTTTAAATACAT[A/C]CCTGCCAATGGAACA | 1161 |
rs371314040 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877312 | TTGAAGTCAGGTAGT[A/G]TGATGCCTCCAGCTT | 1161 |
rs371320180 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891929 | AAGTGAGATCAGTCA[A/C]TTAGTTACCAACACT | 1161 |
rs371337487 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908755 | ATAGACTGAAGTGTG[A/C]AGCTGTGGTTGCCCA | 1161 |
rs371349262 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876581 | ACCATTCTAACTGGT[A/G]TGAGATGGTATCTCA | 1161 |
rs371357663 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938090 | ATATATATATATTTT[A/T]TTTTTTTTTTTTTTA | 1161 |
rs371386047 | snp | A/T | 5.02197e-05 | 0.00501072 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945427 | TGGTCAGTGATTGCG[A/T]GGTCAGTAAAGGAGG | 1161 |
rs371402610 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904846 | GATGACTATAAACTG[C/T]TTCCTCAAAATTAAA | 1161 |
rs371518716 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934434 | GTTGGGATTGTTTAT[C/T]TTTTTCTTGATTTGA | 1161 |
rs371791493 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880546 | TAGTCCCATATTTCT[G/T]GGAGGCTTTGTTCAT | 1161 |
rs371792015 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917563 | AGATGTGCAGTAAAG[A/G]CAAGGTAAATAGAAA | 1161 |
rs371826101 | in-del | -/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886187 | GAAACCACCTTTAAA[-/C]CAGCCTCTATCTTCC | 1161 |
rs371826720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940496 | CTGGCTAGATGGCCA[A/G]AACAGGGAGTCCCAG | 1161 |
rs371833950 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914723 | AGCCCGGAGTTTGAG[A/G]TTATAGTGAGTTATA | 1161 |
rs371862984 | in-del | -/CACGTAG | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920827 | TTATGTAGCACGTAG[-/CACGTAG]AATAGGTGAAAATAC | 1161 |
rs371894373 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879736 | GATCTTCCTCCATCC[C/T]TTTATTTTCAGCCTA | 1161 |
rs371908583 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913565 | GATTCATTGATTTTT[G/T]GAAGGGTTTTTGGTG | 1161 |
rs371916112 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926960 | GTATCTGATGGCACT[G/T]ACATTAACTATGAGA | 1161 |
rs371959385 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877889 | GCCTGATTGCCCTGG[A/C]CAGAACTTCCAACAC | 1161 |
rs371960913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941683 | AACCAGAGAAAAATG[A/G]TAAATTACCTATAGG | 1161 |
rs372028035 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945170 | GCCGACCTGACTTCT[C/T]CGCCTCGGTGGGCTG | 1161 |
rs372110212 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899325 | ACTTTTTAAATGGCA[C/T]TGAATATGTATAGTT | 1161 |
rs372113379 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927889 | GACCATGGTGGAAGC[C/T]GGAAGTAAAAAGTGG | 1161 |
rs372134417 | snp | A/G | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873628 | GTTGCAGTGAGCTGA[A/G]ATCAAAACACTGCAC | 1161 |
rs372157876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938301 | ATTATTTCCAGTTTC[C/T]ATACCTTATGATCAA | 1161 |
rs372171306 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894021 | ACAGAGTCTTGCTCT[G/T]TCGCCCAGGCTGGAG | 1161 |
rs372173688 | snp | C/T | 1.65007e-05 | 0.00287229 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887415 | CTTTAGAAGTCACTG[C/T]ACCATTTGTGAAAAT | 1161 |
rs372212490 | snp | A/G | 1.65734e-05 | 0.00287862 | missense, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918285 | ATGTATTTGTATCCC[A/G]TACTTTCAGAGTTTT | 1161 |
rs372236542 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945016 | CCCAGCATATCGTGT[C/T]CTCACACCGGCTGGA | 1161 |
rs372237310 | snp | C/T | 1.64868e-05 | 0.00287109 | splice-acceptor-variant | ERCC8 | GRCh38.p7 | 5:60887522 | CCACTATAAAGTTCC[C/T]ATAACATAGAAGGCA | 1161 |
rs372306454 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910523 | TTGAACATGGAATAC[A/C]CCACATTTATTTAGG | 1161 |
rs372307780 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878002 | AGTATGATATTGGCT[A/G]TGGGTTTGTCATAGA | 1161 |
rs372313824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893790 | TTTATAGTTAAACAT[C/T]TTTTCATACACATAA | 1161 |
rs372370196 | snp | C/T | 5.05766e-05 | 0.00502849 | intron-variant, missense | ERCC8 | GRCh38.p7 | 5:60903587 | ATACACTGTTAGTAA[C/T]GTTTCTTTTTATTGA | 1161 |
rs372406262 | snp | C/T | 0.00013348 | 0.00816837 | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918427 | ACATTAACTGACTTA[C/T]GTGAGTTTCAAAACT | 1161 |
rs372408884 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937584 | AAGTTGGGGAAGGCC[A/G]GCAGCCAAAGGCTTC | 1161 |
rs372414756 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911815 | TTCTACATATGGCTA[A/G]CCAGTTTTCCCAGCA | 1161 |
rs372430053 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889594 | GCATGAGCCACTGTG[A/C]GCAGCCATTGTCACG | 1161 |
rs372581358 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60887740 | GTCAGAGCTTACTAA[C/T]GGTGTGAAAATTTTA | 1161 |
rs372586432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932593 | GACTCCACTAGGAAA[G/T]GATTCTTGGAAGCCT | 1161 |
rs372601364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878115 | AACGCCTTTTCTGCA[G/T]CTATTGAGATAATCA | 1161 |
rs372673262 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899745 | GAGAAGAAATAAATG[A/T]TACATTGACATATGT | 1161 |
rs372684577 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895389 | GGCAGTAGCAGTATA[A/G]TGGGTTAAATATTAA | 1161 |
rs372707555 | snp | A/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922095 | TGTGTAATAAGATTG[A/T]CTGCTGGAGTTCTCA | 1161 |
rs372826255 | snp | C/G/T | 0.000102865 | 0.0071709 | intron-variant, synonymous-codon | ERCC8 | GRCh38.p7 | 5:60903625 | ACTCAAAGTAGTTGC[C/G/T]GTTTGAAATAAAATA | 1161 |
rs372828060 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907438 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 1161 |
rs372897188 | in-del | -/TA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886960 | AGAAATGTTTACACA[-/TA]GTTATTAATGACATG | 1161 |
rs372934870 | snp | A/G | 0.00117389 | 0.0241985 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898431 | TAGTTCAGTTTATCT[A/G]TTCTTGTATTCAGGA | 1161 |
rs372943072 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890242 | GTTCATTCTATCAGT[A/C]TTTAACTTACGTGAG | 1161 |
rs372944223 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891117 | AATAAGGTTACTCAT[C/G]TCTGAAATCTGAATT | 1161 |
rs372945700 | snp | C/G | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873658 | CTCCGGCCTGAGCGA[C/G]AGAGTGAAACTCCAT | 1161 |
rs372977536 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904685 | ATATATATATATATA[A/T]AATTGTGATATTCCT | 1161 |
rs373039343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929290 | ATGTTTCTTAAAGAC[A/G]GACAGAAATAAAAAA | 1161 |
rs373135152 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936163 | ACCTAAACTTTTTTT[A/G]GTAACTTTTTTATTA | 1161 |
rs373174008 | snp | C/T | 0.000742335 | 0.0192514 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928888 | TCAACAGGTTCAATG[C/T]CAAGGGTGTTAATTC | 1161 |
rs373203544 | snp | C/G/T | 3.30514e-05 | 0.00406507 | missense | ERCC8 | GRCh38.p7 | 5:60890990 | AAACAGCAATGGTGC[C/G/T]ACCATATGGTACAAA | 1161 |
rs373211136 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906868 | TGAAGGCTAAAGGCA[A/G]GAGGGGGTGGTGGCT | 1161 |
rs373214701 | in-del | -/ACATAC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938043 | CATACATACATACAT[-/ACATAC]ATATATATATATATA | 1161 |
rs373221993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901334 | TAGACACCGAAAATT[A/G]TTAAGTCTCTTTCAT | 1161 |
rs373225014 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911343 | TGCATTTCTCTGATG[A/T]CGAGTGATGACGAGA | 1161 |
rs373228647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935574 | ACTTCCAGCACTATG[C/T]TGAATAGAAGTGGTG | 1161 |
rs373276259 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943395 | CGTGAGAAATAGCAT[A/C]AAAGTTTGCTACTAG | 1161 |
rs373281111 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915303 | TAGAAATTATATAGA[A/C]AAAATTGGGAGAGAT | 1161 |
rs373296539 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904920 | GTTTAAGTATAAAAA[-/A]CAAAGCAATAAATTT | 1161 |
rs373303052 | snp | C/T | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873501 | CCAACATGGTGAAAC[C/T]CCATCTCTACTGAAA | 1161 |
rs373318528 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875823 | TGCCTCAGCCTCCCA[A/G]GAAGCTGGGACTACA | 1161 |
rs373334122 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931280 | AATATTTGGCTGAGC[C/T]GCATTTGAACTTTAA | 1161 |
rs373405843 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912005 | TGTAGCCTGGTAGTA[C/T]AGTTTGAAGTCAGGT | 1161 |
rs373442446 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876269 | CACATTTTCTTAATC[C/T]AGTCTATCACTGATG | 1161 |
rs373448911 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896056 | CAATGGCATGCTCTC[C/G]GCTCACCGCAACCTC | 1161 |
rs373515505 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885142 | TCACCCTCTTAAGTA[A/G]CTGGAACTATAAGTG | 1161 |
rs373539247 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907029 | GACTTAGCCAATCCC[C/T]TGCTCTCCTCAGGTA | 1161 |
rs373564291 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925075 | TTTTATAATGATTTT[G/T]TAGGAACTTTGACCT | 1161 |
rs373674319 | in-del | -/C | 0.469642 | 0.119404 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944706 | GAGCCCGCGGGGGAA[-/C]CCCCCCCCCACCCCC | 1161 |
rs373688537 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893448 | CTCGATTGGCATGAT[C/T]ATTGGAGTGAACAAA | 1161 |
rs373740060 | in-del | -/AAC | | | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874350 | TCACAACTGAGGTAC[-/AAC]GACTTGTGTTACTTG | 1161 |
rs373748450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897220 | CTTAGTGAAGCCTAC[C/G]CTGACTTCCCTATGT | 1161 |
rs373783755 | snp | A/G | 1.64977e-05 | 0.00287203 | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904854 | TAAACTGTTTCCTCA[A/G]AATTAAATACATCTG | 1161 |
rs373823905 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881618 | CTCAGACTGCTGTGC[C/T]AGCAATGGGCGAGGC | 1161 |
rs373924698 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877698 | GGTGTATAAGAATGC[-/T]TGTGATTTTTGCACA | 1161 |
rs373930268 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904975 | TAGCTATTTTTAAAT[C/T]GACTGTTAGCAATTC | 1161 |
rs373945885 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879522 | TCTCTTTTTAGGTCT[C/G]TAAGGACTTGTTTTA | 1161 |
rs374036813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934926 | CCGTTGGTCTATATG[C/T]CTATTTTTATTACCA | 1161 |
rs374110434 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882027 | TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCACC | 1161 |
rs374117783 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892419 | AGAACTTGGTCATTT[C/T]CTTAATTCTCAGCAC | 1161 |
rs374143395 | snp | G/T | 0.000576792 | 0.0169724 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904758 | GGGAGAAAGTTTTCA[G/T]TATGTCAAAAGACAA | 1161 |
rs374154824 | snp | A/G | 3.35666e-05 | 0.00409661 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60874636 | TTCTTCATCACTGCT[A/G]CTCCAGGCATCTTCA | 1161 |
rs374312359 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882648 | AGCCTTGGCCTCCCA[A/T]AGTGCTGGGATTACA | 1161 |
rs374346406 | snp | C/T | 1.72246e-05 | 0.00293462 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945287 | ATTTGTTCCGCGCCT[C/T]GTGGAGATCGCTGTC | 1161 |
rs374386779 | snp | A/G | 0.000153988 | 0.00877328 | missense | ERCC8 | GRCh38.p7 | 5:60891031 | GAACTGCAGCCACAG[A/G]AGACAGTGAATTTCA | 1161 |
rs374391258 | in-del | -/CA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890522 | AATAGATCATCCACA[-/CA]TACATAAACCAACAT | 1161 |
rs374406177 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920079 | GAGTTAGCCATTATT[A/C]AAAGCTGAGGAGTTG | 1161 |
rs374452530 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944846 | GTGGCAGGAGAGCGA[A/T]GAGACGGGAAAGTGT | 1161 |
rs374505037 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926852 | AAATTTTAATCTTAA[A/T]TGATATGGTATTTAC | 1161 |
rs374507957 | snp | A/T | | | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60902878 | TTTTCCAATTTCTCA[A/T]AAAGTTATAAGAGAA | 1161 |
rs374522937 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888150 | TGGCTTTTTTCCTCT[G/T]CTGTTTAATACAATT | 1161 |
rs374547965 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909246 | ATGCCCTATTCTGAA[A/G]AAAAAAAAAAAAAAA | 1161 |
rs374593227 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901912 | CCTATATTACACCTA[C/T]CAGAGATGTACCTCT | 1161 |
rs374609381 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879047 | TGCTTTGAATGTGTC[C/T]CAGAGATTCTGGTAT | 1161 |
rs374611680 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904784 | GACAAAAGAATACAC[C/T]TACAAACCTGCTACC | 1161 |
rs374630066 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927976 | TAAAATAAAAATTCT[G/T]GGGGAAATGCTAAAC | 1161 |
rs374636945 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944154 | TTATTCATTCTTCTC[C/T]TTTTGTCATTCACGT | 1161 |
rs374684914 | in-del | -/A/ATAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908584 | TATATATATATATAT[-/A/ATAT]TTTTTTTTTAAATAA | 1161 |
rs374721303 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883652 | GTTGTCAGCAAGTGA[C/T]TATACATTGACACAA | 1161 |
rs374726306 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915653 | TCCAGAGACCACCCA[C/T]ATTTCTTGGCTTGTG | 1161 |
rs374740906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886678 | CTGCACTCCAGCCTG[A/G]GCGACAGATTGAGAC | 1161 |
rs374785056 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890151 | GTGTCAGGCACAAAT[C/T]AGGCAATCAGTATTA | 1161 |
rs374821511 | in-del | ATT/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907355 | CATAGAAACATGATT[ATT/C]TTTTTTTTTTTTTTT | 1161 |
rs374898751 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60887040 | TGAATGTCCAACCAT[A/G]ATATGAACTATGTTA | 1161 |
rs374963068 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877848 | TTCCTCTTTTCCTAA[C/T]TGAATACCCTTTATT | 1161 |
rs374996017 | in-del | -/CTTA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901129 | ATAATTCTTCTTCTA[-/CTTA]AAGTTTTATGAAAAT | 1161 |
rs375016674 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908439 | TTCCTGTAAATCCCT[C/T]AAACTCAACAAATCG | 1161 |
rs375207363 | snp | A/G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60921794 | TAAAGAAAAAGAAGG[A/G/T]CATAATCACAAGTTT | 1161 |
rs375245148 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918335 | AACATGCCAGTGTCA[C/T]GAGGATACCACTGTA | 1161 |
rs375290208 | snp | C/T | 0.000115558 | 0.00760038 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887550 | GCAAAGATGATACTG[C/T]GGATCAAGAGCTGAT | 1161 |
rs375459590 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883455 | TGAACATATTCATCT[A/G]TATCTCACCAGGTTG | 1161 |
rs375518465 | snp | C/G | 1.66615e-05 | 0.00288626 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928975 | CTTAAAAATAAAAGG[C/G]GGAGAAAGAAATTAA | 1161 |
rs375562475 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895003 | GTGAAATCCCATCTC[C/T]GCAAAAAACACAAAA | 1161 |
rs375581283 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877950 | TCCCTGTCTTGTGCC[A/T]GTTTTCAAAGGGAAT | 1161 |
rs375656461 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936959 | CAGATTCTTTTGTCC[C/T]ACGAGGTGCTCCCTT | 1161 |
rs375685574 | snp | A/G | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919309 | ATGATGGTTGGTGAA[A/G]CTGGGTGATTGATAC | 1161 |
rs375699552 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893727 | CTGGCGGCGCCCGAC[C/T]CCGCCCACTGGGCAG | 1161 |
rs375714342 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878196 | TTGTGTATGTTGAAC[C/T]AGCCTTGCATCCCAG | 1161 |
rs375746947 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912222 | ATTCTTCCTATCCAT[A/G]AGCATGGAATGTTCT | 1161 |
rs375833663 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935772 | GATTTTGTCAGATGC[C/T]TTTTCTGCATCTATT | 1161 |
rs375935908 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60887198 | TCAAATTATTTTTAC[A/G]GAAATTACCAAGAAA | 1161 |
rs375961740 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882148 | GCCCGGCTTAGAAAC[A/G]TTTTTTAATGGTAAC | 1161 |
rs375974774 | snp | C/T | 4.9543e-05 | 0.00497685 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928867 | TAATAAACTTACTAT[C/T]TCCCTTCAACAGGTT | 1161 |
rs376009266 | snp | G/T | 1.70217e-05 | 0.00291729 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945067 | AGAGCTCAGGGGCGG[G/T]ACTGGAACAGCAGAG | 1161 |
rs376012884 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877710 | TGCTTGTGATTTTTG[C/T]ACATTGATTTTGTAT | 1161 |
rs376014896 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896500 | CAGGTGTGAGCGACC[A/G]TGCCTGGCCTGTCAA | 1161 |
rs376022496 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892023 | TTTATCTGCACATTT[C/T]TGTAAATTCTTACTC | 1161 |
rs376037176 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940634 | GATCTAACCCTGAGT[C/T]GTATACAAAGGATTT | 1161 |
rs376045901 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945190 | TCGGTGGGCTGGGTC[C/G]GCGGCTGGAGCATTA | 1161 |
rs376063046 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888056 | CACAGCCTATGTCAA[C/T]GTCTACAGATATGCT | 1161 |
rs376080864 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907477 | CCTGTGTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 1161 |
rs376189861 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911888 | GTCAGGTTTGTCAAA[A/G]ATTGGATGGTTGTAG | 1161 |
rs376273747 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915322 | ATTGGGAGAGATTCT[A/G]CGTTATGTTATCCTC | 1161 |
rs376333661 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923390 | ACTGTGTTTTTTTAA[-/A]TGGGATTTTTCAATA | 1161 |
rs376383083 | snp | A/C/T | 5.24199e-05 | 0.00511934 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922009 | CGATGCAAAAAATAC[A/C/T]CAACTATTTACAAAT | 1161 |
rs376401893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60924475 | TTGACTCACATTTTA[C/T]TTCCTTGAGCATCTT | 1161 |
rs376480709 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896147 | TGCGCCACCATGCCC[A/G]GCTAATTTTGTACTT | 1161 |
rs376481715 | in-del | -/GTGT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904622 | TGTTGAATATATATA[-/GTGT]GTGTGTGTGTATATA | 1161 |
rs376532012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893218 | ATTCTACCACCTCAC[A/G]GACTCCTTGTAATAA | 1161 |
rs376599291 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896443 | TCTTGATCTCCTGAC[C/G]TCGTGATCCACCCAC | 1161 |
rs376619221 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910207 | AATTAATGTCATCAA[C/T]GGGTACATTTCTTGA | 1161 |
rs376657416 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882391 | CAAATGTCCAGAAGC[A/G]AAACTATTATTATTA | 1161 |
rs376669896 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926627 | TTGTAGTTCAGTTAC[C/T]CTAATTGTGTACATA | 1161 |
rs376670345 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907953 | TTTAATCTGTCAGTA[-/G]CATTCAACACAATTG | 1161 |
rs376747316 | snp | C/T | 6.60906e-05 | 0.00574812 | upstream-variant-2KB, synonymous-codon | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945375 | CCCGCAGTACAAGAA[C/T]TGGAGAGGTGAGGTG | 1161 |
rs376787358 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907446 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 1161 |
rs376796317 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898118 | GTAAGGGTGGGTTGT[A/C]CTGAGTTGAGAATTA | 1161 |
rs376806322 | snp | G/T | 0.00175047 | 0.0295325 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939367 | TTTGATTAACGTTCT[G/T]TCCTAATTTTTTTCC | 1161 |
rs376840512 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911108 | GGGTACATGTGACAA[C/T]GTGCAGGTTTGTTAC | 1161 |
rs376853894 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907149 | TTTCACTTGTATTCT[G/T]CTCTGCAGTATTCCT | 1161 |
rs376931655 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902052 | CACAATGCTTGGCAC[A/G]TGGGAGGAAGTCATT | 1161 |
rs376937131 | snp | C/G/T | 0.000149412 | 0.00864207 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902415 | TTATTAATTACTAAC[C/G/T]TCAAAAGCAAATAAG | 1161 |
rs376948846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913888 | GTTGTTCAGTTCCCA[C/T]GCAGTTGTGTGGTTT | 1161 |
rs376992282 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932951 | TGGTGTCTTTTAAAA[-/A]TCACCTTTCCAATCT | 1161 |
rs377001963 | snp | C/T | 1.6525e-05 | 0.00287441 | missense | ERCC8 | GRCh38.p7 | 5:60890992 | ACAGCAATGGTGCTA[C/T]CATATGGTACAAAAA | 1161 |
rs377130800 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901818 | GCAGATAAATATGCA[A/T]TACTCTTTTTCTCCA | 1161 |
rs377155839 | snp | C/T | 1.67108e-05 | 0.00289052 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903746 | CCGGTTTAAGATAAT[C/T]TTATCATAAGTCATC | 1161 |
rs377205472 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906653 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 1161 |
rs377257420 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892240 | TCCAATCTTATATAC[A/G]GTAGCTTTATCTTCA | 1161 |
rs377277599 | snp | C/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945496 | ACACTTAGGGTGTCA[C/T]CGGAGAGAATTTCCC | 1161 |
rs377311968 | snp | C/T | 6.59968e-05 | 0.00574404 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928907 | GGGTGTTAATTCCAC[C/T]GCCGTGGATTCTTTC | 1161 |
rs377387148 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930970 | AAAAATTAGCCAGGT[A/G]TGGTGGGGCATGCCT | 1161 |
rs377431648 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924629 | TGTTTTAATATTTAT[C/T]CTGCTCTTTTGCCTT | 1161 |
rs377473708 | snp | A/G | 1.71337e-05 | 0.00292687 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60891063 | TCCTTTTTTACTGTT[A/G]TTACAAACTTTTCCA | 1161 |
rs377555714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912024 | TTGAAGTCAGGTAGC[A/G]TGATGCCTCCAGCTT | 1161 |
rs377612124 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60880955 | CTGACTTTTAGAGTT[C/T]CCAGTTTTTCTGCTC | 1161 |
rs377651161 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896112 | CTGCCTCAGCCCCCA[A/G]ATAGCTGGAATTACA | 1161 |
rs377665946 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878777 | CTTCTTTATTACTCT[C/T]GCTAGTGGTCTATCA | 1161 |
rs377745901 | snp | A/G/T | 0.000119469 | 0.00772805 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874608 | AAAAAGGTACTAAAG[A/G/T]TGATATTCATCCTTC | 1161 |
rs377759162 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923693 | TTGAACAAATTCTTT[A/G]TGTCTCTTTTGGAAG | 1161 |
rs386403913 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908590 | TATATATATTTTTTT[-/T]TTTAAATAATGGCTT | 1161 |
rs386688453 | multinucleotide-polymorphism | AGG/GGC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884401 | GAATGGCGTGAACCC[AGG/GGC]AGGCGGAGCTTGCAG | 1161 |
rs386688454 | multinucleotide-polymorphism | CCC/TGT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884430 | GCAGTGAACCGAGAT[CCC/TGT]GCCACTGCACTCCAG | 1161 |
rs386688455 | multinucleotide-polymorphism | AGAA/TTCT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940512 | AACAGGGAGTCCCAG[AGAA/TTCT]CTGGGAAGCATCCAG | 1161 |
rs397686987 | in-del | -/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908231 | GATTTTTTTTTTTTT[-/T]GGTTTGGAAGGTTTG | 1161 |
rs397690220 | in-del | -/A | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914809 | AAAAAAAAAAAAAAA[-/A]GGATATTGACTTTTA | 1161 |
rs397723873 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898805 | CATTGAAAAAAAAAA[-/A]CAGGGAAAGGATGAC | 1161 |
rs397781271 | in-del | -/TA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886076 | ATATGTATATATATA[-/TA]CAAACATTGTTTTTA | 1161 |
rs397881917 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894002 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 1161 |
rs397881928 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907372 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCGCTC | 1161 |
rs398108984 | in-del | -/TT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875901 | TTTTTTCTTTTTTTT[-/TT]ATTATACTGTAAGTT | 1161 |
rs527250788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926216 | CATCTGATTTTGAAC[A/G]AAATACAATTAAATG | 1161 |
rs527338771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878775 | TTCTTCTTTATTACT[C/T]TTGCTAGTGGTCTAT | 1161 |
rs527390747 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876099 | TGTTCTTACTGTTCA[A/G]TTCCCACCTATGAGT | 1161 |
rs527417803 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916958 | AACAAGTATGAAAAT[A/G]ATATTATAAAGTAGT | 1161 |
rs527424338 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946937 | ATAGCATAATGTAGC[G/T]GAGATTCATCCATGT | 1161 |
rs527438755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913043 | ATTTGGGATATTGGT[A/G]TAAATTTCTCTTTTT | 1161 |
rs527489899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896934 | TTCTCCACTCACAAG[A/C]CTTTAGTGGCTTTCC | 1161 |
rs527528046 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940253 | GACTCTGAAAAGTAA[A/C]CAGCCACAGACAATC | 1161 |
rs527576439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934195 | GTACTAGTTGACATT[C/T]CCACTGGCAGTGGAA | 1161 |
rs527580929 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895978 | AATGTCATATTAATA[C/T]TTCTTTTCTTTTCTT | 1161 |
rs527590316 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60928414 | TAGCTAAGGCAACTG[A/G]TAATTCGAAAGGTTA | 1161 |
rs527647101 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935139 | GCAGTATGGTTATTT[C/T]CGCAATATTGATTCT | 1161 |
rs527752850 | snp | A/C | 1.6651e-05 | 0.00288535 | splice-donor-variant, missense | ERCC8 | GRCh38.p7 | 5:60903647 | AATAAAATAAAAATA[A/C]CCTGTAGAATGTGAG | 1161 |
rs527780749 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906415 | AGGTGGTTGAGTTTT[C/G]GAGAAGGGCTATTAT | 1161 |
rs527813874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904694 | TATATAAAATTGTGA[A/T]ATTCCTCTGGGTTAA | 1161 |
rs527817063 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896294 | CGATCTCGGCTCACC[A/G]CAACCTCCACCTCCC | 1161 |
rs527874286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881565 | TCAGCAATGGCGGGC[A/G]CCCCTCCCCCAGCCT | 1161 |
rs527879176 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946218 | TTTTGGGCGAAGAGG[C/T]GTGGGTTAGAATCTC | 1161 |
rs527910170 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60924489 | ATTTCCTTGAGCATC[C/T]TGGATAAGAAGCTTC | 1161 |
rs527918086 | in-del | -/TAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908583 | ATATATATATATATA[-/TAT]TTTTTTTTTTAAATA | 1161 |
rs527943190 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876974 | CCTATGTCCTGAATG[C/G]TAATGCCTAGGTTTT | 1161 |
rs527964015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925393 | TTCTGTACTGGGGGC[A/G]CACTTTGACTGGTTA | 1161 |
rs527972511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917649 | AATGAGATGTGATCA[G/T]GTTCAGTTGGGACCA | 1161 |
rs528000003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877487 | GCCATTTTCACAATA[C/T]TGATTCTTCCTACCC | 1161 |
rs528022120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910800 | TTTCTACGTTCATAA[C/T]CATGTCTTCTGTGAA | 1161 |
rs528023398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918423 | ATTTACATTAACTGA[C/T]TTATGTGAGTTTCAA | 1161 |
rs528037131 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915397 | GATCATATCAATTCA[A/G]ACATAAAGCTTGTCT | 1161 |
rs528087648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908333 | GGGACACTCAGTACA[C/T]AGTGAGGCACAAATC | 1161 |
rs528099114 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944122 | ACTTCTTATACAAGG[C/T]ATAGATCTGGGAATC | 1161 |
rs528109055 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894653 | CAGGCCCCACCCCAA[A/T]CCTACCGAAAATAAT | 1161 |
rs528208612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893516 | CCATTTTGTTTTGCA[A/G]GCTTCTTACAGCCCT | 1161 |
rs528311994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874794 | AGCAATTACATTATT[G/T]TGGAAGAAAATGTAT | 1161 |
rs528369656 | snp | A/C | 3.30491e-05 | 0.00406491 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922125 | AAGGTCATAAAGTAC[A/C]ATCACACCATCTGAA | 1161 |
rs528373631 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875359 | ACATAGGTTTCCCTC[A/C]GGGATTTGTCTGAAG | 1161 |
rs528436206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915044 | CACTGGCTTGTAATT[C/T]TCCATATAATGTCCT | 1161 |
rs528471756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892401 | CGGTATCCTCGATGT[C/T]AAAGAACTTGGTCAT | 1161 |
rs528520488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942537 | TGCTGAGTGAAAGAA[G/T]CCAGACAAAAAAGAT | 1161 |
rs528550318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918800 | TTATTGAATGCCTCA[C/T]ACACCTCCATGGTAT | 1161 |
rs528580299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879549 | TTTATGAATCTGGGT[C/G]CTCCTGTATTGGGTG | 1161 |
rs528594052 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941485 | TCTAGAAGGAGAAGA[A/C/G]AAAGAGTGTAGTGTT | 1161 |
rs528603804 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884448 | GCCACTGCACTCCAG[A/C]CTGGGTGACAGAGCC | 1161 |
rs528616659 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885078 | AGTATAGTGGTGCAA[C/T]TGTGGCTCACTGTAG | 1161 |
rs528672764 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934589 | CCTATCTATTTATCT[C/T]TGTTTTTGTCGTGTT | 1161 |
rs528691491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913720 | TTCCTGCTTTCTCTT[C/T]TGGGCATTTAGTGCT | 1161 |
rs528694682 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888567 | AAGAGATATTGAAAG[C/T]AGCAACATTTAAATT | 1161 |
rs528703906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905606 | GGTAAATATTTTAGG[C/T]TTTCAGGACCAACTA | 1161 |
rs528763516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906280 | AGCTCAAGCAATCCA[C/T]CCTCCTTGGCTTCCC | 1161 |
rs528848578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939033 | TAAAAATTAATCTGA[C/T]AATATATGCTTCTTA | 1161 |
rs528913012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939488 | TACTTCTTTTTTTTA[A/G]TTTTTAGATAACTTT | 1161 |
rs528926931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932252 | AAACATAGGTTAACA[C/T]AGCAGGCCTGAGACG | 1161 |
rs528941688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889187 | TATTCGATGAAGGTG[A/G]TATGTGCCAGGCTCC | 1161 |
rs528970733 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876990 | TAATGCCTAGGTTTT[A/C]TTCTGGGGTTTTTAT | 1161 |
rs528987900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924717 | CTATATATACACCTC[C/T]TGAATTATTTTCCTC | 1161 |
rs529008774 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906045 | GAAAAAATCCTGAAA[A/G]GATATCTCAAAAGGC | 1161 |
rs529089806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910397 | AACATTAGAATTAGC[A/T]AGTCAATTTTCAAAA | 1161 |
rs529143560 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878343 | TTCTCTTTTTTTGTT[C/G]TGTCTCTGCCAGGCT | 1161 |
rs529176390 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894782 | ATAATTTTGATAAGC[G/T]TGGGGTGAGTGTAAA | 1161 |
rs529207242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931111 | ACAAAGCAAGCAAGA[C/T]TCCGTCTCAAAAAAA | 1161 |
rs529209393 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923108 | ACTGAAGCCTTACTT[C/G/T]TGGGAGTAAAAGAGG | 1161 |
rs529239440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895604 | TATTCAGTAAGTTCC[C/T]AGATTAATTCCTATA | 1161 |
rs529284009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881180 | GCAGAACAGTGGATA[C/T]TGGTGAATAGCAAAT | 1161 |
rs529286041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876147 | TGGGTTTTTGTCCTT[A/G]CAATAGTTTGTTGAG | 1161 |
rs529322201 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911873 | CCATTTCTTGTTTTT[C/G]TCAGGTTTGTCAAAG | 1161 |
rs529340085 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881225 | GTTCCTCTGGGAGTT[C/T]TGTCTCAGAGGTGCA | 1161 |
rs529350262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876522 | CTGTTCCTATTTCTC[C/T]ACATCCTCTCCAGCA | 1161 |
rs529372332 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916709 | TATTTAGTTTGAATT[A/T]TTAGAAGTATATTAA | 1161 |
rs529425445 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938542 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 1161 |
rs529436850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909479 | CCTTTTGCTACCCTA[C/G]AGACAGCAAGGTCAA | 1161 |
rs529467579 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889143 | ATATCACAGAAGTGA[C/T]GTCCCATAACTGGGA | 1161 |
rs529538907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930553 | TAAGAGCAAGACTCC[A/G]TCTAAAAACAAAAAC | 1161 |
rs529597588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927729 | ATGTCTGCATGTTTC[A/G]TAAGTGAGTGCCCCC | 1161 |
rs529669852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879332 | GTGTGGTGCTGAAAA[G/T]AATGTATACTCTGTT | 1161 |
rs529706793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913139 | ATTCCTTCTTTTTCT[A/G]TTGATTGGAATAGTT | 1161 |
rs529730077 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924901 | TTCTGAGGTTTTCTA[A/G]TAACTTAACATTATT | 1161 |
rs529752367 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874030 | GATTTTCACAAAGTT[A/G]AAAGCCTCCTGTGAT | 1161 |
rs529887588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882540 | GCTGTGACTACAGGC[A/G]CATGCCACCGGCGAA | 1161 |
rs529898633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883335 | TAAAAATGTTGTAGA[C/T]GGATGTGGTACACAT | 1161 |
rs529915268 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938711 | AAATGTACCACTGAC[A/T]TACAAAAAGTATGTA | 1161 |
rs529957736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878899 | CCTTAGTTATTTCTT[A/G]CCTTCTGCTAGCTTT | 1161 |
rs530170931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897893 | TAGCACTCAAAAAGT[G/T]TCAGATTTTGGAACA | 1161 |
rs530176676 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926800 | TCTTGCCATACAGAT[C/G]TATTATCAATATAAA | 1161 |
rs530332230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918502 | GAATGGCCAAACCGA[A/G]ATCACATGCCTGTGT | 1161 |
rs530365331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903821 | CACTGTATCCATGCA[A/G]AAATATGAAGATATA | 1161 |
rs530401937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919062 | TCTTGATTCAAACAA[A/C]CTGGCTTTTAAGAGA | 1161 |
rs530485527 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894093 | GGGTTCACGCCATTC[G/T]CCTGCCTCAGCCTCC | 1161 |
rs530488384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901930 | GAGATGTACCTCTAT[G/T]AAAGCATTTTTCTGG | 1161 |
rs530546302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894458 | TATGCAGAAAACAGG[G/T]ATAAAGGCTAAGTGT | 1161 |
rs530555738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886857 | CAATTTTTGAACAGA[C/T]ATTTACCTTGATGTT | 1161 |
rs530658530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876034 | CCCTCCCCCCTACCC[C/G]CACCCCACAACAGGT | 1161 |
rs530679736 | snp | G/T | 1.66275e-05 | 0.00288331 | stop-gained, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922155 | ACCACCTGATAACAT[G/T]CTGATAATAAAAAAG | 1161 |
rs530691417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908391 | GAATTCTGGGTATGT[A/G]TAGATCGATTCCTGG | 1161 |
rs530752367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900318 | CATTTTCTTTCAAGT[A/C]AGCAAAAAGAAGAAA | 1161 |
rs530776352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936580 | TTTGGGTTTGGTTTG[C/T]TGTTTCTCCAGTTCC | 1161 |
rs530810074 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884532 | GTATGTGTTTTTTTT[G/T]TTTTTGTTTTCTAGT | 1161 |
rs530844598 | in-del | -/T/TT | 0.552067 | 0.179928 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875893 | TTTATTTATTTTTTC[-/T/TT]TTTTTTTTATTATAC | 1161 |
rs530860082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879965 | CTTCCTAGCCTTGAT[A/G]GTCTTTACAATTTGG | 1161 |
rs530925582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874850 | AGAAACAACCCATAT[A/G]CAATATAAGATAATG | 1161 |
rs530964280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937473 | TGAGGCTTGCCGCTG[C/T]TGCTGTGGTAGATGG | 1161 |
rs530967114 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917522 | TGTAGAAAATGTAGA[A/G]GGTAAGGCAGTGATT | 1161 |
rs530992320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893719 | ATGCCAGCCTGGCGG[C/T]GCCCGACTCCGCCCA | 1161 |
rs531013013 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909654 | CTAGCTTACTTTATT[A/G]TAACAACGCAGTATA | 1161 |
rs531019884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921626 | GTGTTTGGTGAGGGA[A/G]TACCAATATGTTTAG | 1161 |
rs531048063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880325 | ATTTCAGCTTTAGTG[A/C]ATCTGACAATTATGT | 1161 |
rs531049695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941982 | TATATATGGTGCAGG[A/G]GAAAGGGTGATAAGG | 1161 |
rs531060113 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932188 | GGAAAAGGGCAATAA[C/T]ACTATAAAGGGAAAG | 1161 |
rs531113079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942675 | GGATTATAAATGACC[A/G]TCAAAAATTTTTTAG | 1161 |
rs531136875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907150 | TTCACTTGTATTCTT[C/T]TCTGCAGTATTCCTC | 1161 |
rs531193130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892492 | AGAAGCTGATCTTCC[C/T]GCTCACCCAGTCAGC | 1161 |
rs531193318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899544 | CAATTTGTCAATATG[C/T]GTTTATTATGTGGCT | 1161 |
rs531234774 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876321 | TCTTTCCTGTTGTGA[A/G]TAGTGCCGCAATAAA | 1161 |
rs531334909 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881924 | ACCTCAGTTGGAAAT[C/G]CATAAATCACCTGTC | 1161 |
rs531356435 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931682 | ATATTTCATCAAAAC[-/T]TTTTTTTTCATATTT | 1161 |
rs531396959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877758 | GTTGCTTATCAGCTT[A/G]AGGAGATTTTGGGCT | 1161 |
rs531470604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896161 | CGGCTAATTTTGTAC[A/T]TTTAGTAGAGATGGG | 1161 |
rs531485266 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898872 | AACAAGTTTGAGAAA[G/T]CATAATTCTAAAATA | 1161 |
rs531593803 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876884 | AAGCTCTTTAGTTTA[A/G]TTAGATCCCATTTGT | 1161 |
rs531610000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917539 | GTAAGGCAGTGATTT[C/T]AGTAGTCCAGATGTG | 1161 |
rs531664454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889429 | TCTTGCTTCAGCCTC[A/C]TGCACAGCTGGGACT | 1161 |
rs531777299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930680 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 1161 |
rs531807397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910560 | TTTCTCTCAATAATG[C/T]TCTAAAGTTCTCTGT | 1161 |
rs531860226 | in-del | -/G | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919916 | GACAGCCAAATGGGT[-/G]GGATTGTAGGGAACA | 1161 |
rs531872826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923826 | AAAATAGGGGAACCA[A/T]CAAAAATTCTTCACA | 1161 |
rs531897846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938513 | CGTGTGCCACCACAC[A/C]CGGCTAATTTTTGTA | 1161 |
rs531934631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914030 | GTGGTCAATTCTGGA[A/G]TAAGTGCAATGTGGT | 1161 |
rs531935303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881533 | CTTCCCAGCCGCTTT[A/G]TTTACCTACTCAAGC | 1161 |
rs531996827 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914421 | CAACCCCTGCTTTTT[C/T]TTTGCTTTCCATTTG | 1161 |
rs532053883 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876599 | AGATGGTATCTCATT[A/G]TGGTTTTGATTTGCA | 1161 |
rs532056672 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907283 | TTAATGTCTTACCAA[A/C]AAACCTACAAACACA | 1161 |
rs532117330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908224 | AGAGTTCAGATTTTT[C/T]TTTTTTTGGTTTGGA | 1161 |
rs532151546 | snp | A/C | 1.66502e-05 | 0.00288527 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899577 | AATTAAAAATTTTCA[A/C]TGTAAAAAAATACTA | 1161 |
rs532159634 | snp | G/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918615 | TACTAAGGGTCACAA[G/T]GTGAAAGATTCTCTG | 1161 |
rs532223139 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891653 | TGATATTTTTTGGGG[C/G]GGCATATTCTTTTTT | 1161 |
rs532234360 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927841 | ATTTAACCACATGCT[A/T]AAGTAAGATGTTTCT | 1161 |
rs532267228 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879410 | CAGAGCTGAGTTCAA[C/T]TCCTGGATATCCTTG | 1161 |
rs532295007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920665 | TTGTAAAGATGCATA[C/T]TATATGTCCATTTTC | 1161 |
rs532309370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935476 | ATACAATCATGTTAT[C/T]AGTAAACAGCAACAG | 1161 |
rs532406692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897930 | ATTTCAGATTTTCAG[A/G]TTAGGGATACTCAAC | 1161 |
rs532460282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879848 | TGTCTTTTAATTGGA[A/G]CAGTTAGCCCATTTA | 1161 |
rs532497847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892388 | TCATTGACTTGCTCG[G/T]TATCCTCGATGTCAA | 1161 |
rs532543793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923742 | TTATAAAATCTTAGA[C/T]ATTGTGAATGTTATT | 1161 |
rs532551982 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936329 | GATAGTAGCCTTGAA[G/T]GATCTTTTGTATTTC | 1161 |
rs532604744 | snp | A/C | 0.000399281 | 0.0141238 | missense | ERCC8 | GRCh38.p7 | 5:60898309 | GGAACTATTCCAGAG[A/C]CTCATTCGATTATCT | 1161 |
rs532622783 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895058 | TACCTGTAATCCCAG[C/T]TACTCAGGAGGCTGA | 1161 |
rs532651234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941690 | GAAAAATGATAAATT[A/G]CCTATAGGAAAACAA | 1161 |
rs532704526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919198 | TATCTTTTAGAGATA[C/T]AAATAATTATGAATA | 1161 |
rs532736450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905420 | CTCCAGCTTGGATTT[C/T]AAGGTCCAATACCAA | 1161 |
rs532767099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919627 | TTTAACTAATTTTCT[C/G]TTTCCTCTCTTACCT | 1161 |
rs532771135 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912267 | TCCTCTTTTATTTCA[G/T]TGAGCAGTGGTTTGT | 1161 |
rs532832540 | snp | A/G | 0.000214601 | 0.0103564 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887551 | CAAAGATGATACTGT[A/G]GATCAAGAGCTGATA | 1161 |
rs532856522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895454 | TCTTTTTTTTGCCCC[C/T]TATGAATAATGATTT | 1161 |
rs532893808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888118 | CTCCCCAACAAAACC[A/G]AAGAAATATGTTATA | 1161 |
rs532914463 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906100 | TGTTATATGCAGGAG[C/T]AATTGGGGAAGTTAT | 1161 |
rs532946534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894555 | TGGGACAAAAATTAA[A/G]ATTCTTTGCTTGTAC | 1161 |
rs533037295 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909586 | ACTTCCACTGACTTA[A/G]TAGTAAATATATTTC | 1161 |
rs533042595 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945501 | TAGGGTGTCACCGGA[A/G]AGAATTTCCCGAGTT | 1161 |
rs533058652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931306 | TTTAACATTAAATTT[C/T]TTTTTAAATTTACTT | 1161 |
rs533119527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937916 | CTGCCAAGTTAGTCC[C/T]GCCTCCTATACACCA | 1161 |
rs533194792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922213 | TATTTAGTCCATTTA[C/T]TTATGATTGCAAATT | 1161 |
rs533243243 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909360 | GAAGAAGGTTCAGTA[C/G]TGTAATAGAAACATT | 1161 |
rs533285562 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945161 | AGGATGGAGGCCGAC[C/T]TGACTTCTCCGCCTC | 1161 |
rs533316443 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912430 | TGCTTGTGATTTTTG[C/T]ATGTTGATTTTGTAT | 1161 |
rs533366094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892997 | GACCTGATGCTGGGT[A/C]CTGGCCTTGAAAGCC | 1161 |
rs533385049 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930352 | TCACAAGGTTACAAG[A/T]TTGAGACCATTCTGG | 1161 |
rs533408963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892878 | ATCAGGCTGCTTTTC[C/T]CAATATTGGGAAGGC | 1161 |
rs533445143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937568 | ACACAGGTCACCAAG[A/G]AAGTTGGGGAAGGCC | 1161 |
rs533446848 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893716 | CGGATGCCAGCCTGG[A/C]GGCGCCCGACTCCGC | 1161 |
rs533451521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923037 | AAGAAGGGATTTGTT[A/G]CTGGAGCAGTGTGGA | 1161 |
rs533483601 | snp | C/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945992 | AAGGCTCGCTGATTC[C/G]TTTCTCGGGAGTTGA | 1161 |
rs533486585 | snp | A/G/T | 0.00239401 | 0.0345304 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876126 | GAGTGAGAACTTGGC[A/G/T]GTGTTTGGGTTTTTG | 1161 |
rs533572558 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898486 | TTAAACATATTAAAG[A/G]ACAACTACTTGAGTT | 1161 |
rs533576230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899958 | TTCTTTTCCAGATAA[C/G]AAGAACAAAATTTTG | 1161 |
rs533676546 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914847 | ATGTTCGTATCTATT[A/G]AGATGACTAATATGT | 1161 |
rs533677854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926614 | GCTTTATTACATTTT[G/T]TAGTTCAGTTACTCT | 1161 |
rs533702474 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885725 | TTTCTCTTTATTTGG[A/T]TTAAGGACAAAAGAA | 1161 |
rs533794452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911639 | GTTGCCATTGCTTTT[A/G]GTGTTTTAGACATGA | 1161 |
rs533795529 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906392 | GTGGTCTCTCATTAG[C/T]TTTACAAAGGTGGTT | 1161 |
rs533838827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925620 | TTTTACTGCCTCCTC[C/T]AGCAAAAATGCTGGT | 1161 |
rs533858730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904025 | AAGTTTCCCCAACGA[C/T]TATGTGTGAGGTAAC | 1161 |
rs533860337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912414 | TATTGGTATATAGGA[A/G]TGCTTGTGATTTTTG | 1161 |
rs533924190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905008 | CTTAAACATAGGAAT[G/T]TAATACCCCAAAAAA | 1161 |
rs533936236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896692 | GCATGAATTACTTTT[A/C]CTTTGATCAAGTCCA | 1161 |
rs533971771 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946567 | GTGTTAAGTATTTCT[A/T]GACAGGTTGCAAGCA | 1161 |
rs534034940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939225 | AATTTCGCAGCCATA[A/T]TATATATTTCCAGCT | 1161 |
rs534094517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923968 | ATAGTTCATCACCTT[A/G]GAGTGTACACATGAA | 1161 |
rs534098191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877940 | AGAGAGGGCATCCCT[A/G]TCTTGTGCCTGTTTT | 1161 |
rs534202535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909799 | TCTCTACTAAAAATA[C/T]AAAAATTAGCCAGGC | 1161 |
rs534206877 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894952 | GAGGCAGGCGGATCA[C/G/T]AAGATCAGGAGTTCA | 1161 |
rs534264957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902390 | AAATGTAGACTTTTC[A/G]AAATGCTTATTATTA | 1161 |
rs534269490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887872 | CTGAGCTTCAATAAA[G/T]ACTTCAGTGAAGAAA | 1161 |
rs534303026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942217 | TAGCACTCTCACCTA[C/T]TAGTGGTGGGACTGG | 1161 |
rs534358902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936152 | TGTGAGTCTGTACCT[A/G]AACTTTTTTTGGTAA | 1161 |
rs534359703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60916258 | CAATTTCTGTCTCTC[C/T]AGCTTTATGAAATTG | 1161 |
rs534385289 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884348 | GGGCGTGGTGGTGGG[C/T]GCCTGTAGTCCCAGC | 1161 |
rs534410862 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886023 | GTGTTTCCAACTACA[C/T]TATTTATATTTCCAA | 1161 |
rs534483162 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896999 | GGCTTGCAGGGCCCA[C/T]ATGATCTGGCACCCT | 1161 |
rs534549456 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926761 | ACTTTTGCTTCGTAA[G/T]TAATCTTCATGAAAC | 1161 |
rs534600706 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911125 | TGCAGGTTTGTTACA[C/T]AGGTATATATGTGCC | 1161 |
rs534639109 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912738 | TGGGTTTGTCATAAA[C/T]AGCCCTTATTATTTT | 1161 |
rs534647118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898993 | TGAAATATATTAGAA[G/T]GAACTATATAAAACC | 1161 |
rs534659711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939640 | CAGGCACCTGCCACC[A/G]CACCCGGAGCACGCC | 1161 |
rs534688334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893194 | GGACTTCCAGAATCA[C/T]ATCAGAGTATTCTAC | 1161 |
rs534689707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883468 | CTATATCTCACCAGG[C/T]TGTCAATTCTACTGA | 1161 |
rs534689957 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878595 | TCTTCCTCGTTTAGT[C/G]TTGGGAGGGTGTATG | 1161 |
rs534705951 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875448 | AATTTTAATCATCTG[C/T]GGTATTTCAAATCAG | 1161 |
rs534749257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879132 | TCGTTATGTACCCAG[C/T]AGTCATTCAGGAGGA | 1161 |
rs534803913 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60920019 | TAAGAGCTCTACCTC[C/T]TCTTACAGAAAGCAA | 1161 |
rs534916726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897287 | TCCTTTCTTTGCTTT[C/G]CTTTTCTTCATAGTC | 1161 |
rs534979475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890565 | ATTTTATGATTAAAT[G/T]CCTATATTTTATTTC | 1161 |
rs535028536 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896008 | TTTCTTTTTTGAGAC[A/G]GAGTTTTCGCTCTTA | 1161 |
rs535073544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876357 | GTGTGCATGTGTCTT[C/T]ATAGCAGCATGTTTT | 1161 |
rs535102334 | in-del | -/TCTTTA | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919179 | GTTATGCTCATAAAG[-/TCTTTA]TCTTTTAGAGATATA | 1161 |
rs535333276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941311 | GTATTCACTAACAGA[G/T]TGGAGATGGCAGAGG | 1161 |
rs535341210 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943586 | GTGCCCTTGAGATAA[A/G]CCCACATGGAATTTT | 1161 |
rs535390259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938588 | CGAACTCCTGACCTC[A/G]GGTGATCCACCTGTC | 1161 |
rs535420127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887634 | GATTAATGCTATTTC[C/T]ACTCCCTAAAGAAAC | 1161 |
rs535472568 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924001 | TTAGCTTTGCTTTTT[A/T]AAAAAATTTTAATGT | 1161 |
rs535557723 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944641 | AACTTAAGAGAGAAG[G/T]AATACAGTACAACGA | 1161 |
rs535564527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908952 | CAGAAAGGCGTATCT[A/T]TATGTAGACTCTAAT | 1161 |
rs535619924 | snp | C/T | 1.65326e-05 | 0.00287507 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928946 | TGTCTTTATTTAATT[C/T]CAGTCCCAAAACTCT | 1161 |
rs535657759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894197 | CACTGTGTGAGCCAC[A/G]ATGGTCTCGATCTCC | 1161 |
rs535680749 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921864 | GCTTTGGGGAAGACA[A/C]ATGTTAAAAAACTAT | 1161 |
rs535682657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929492 | TGCAGGAGACTGAGG[A/C]AGGAGGATTGCTTGA | 1161 |
rs535753060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930879 | TGGGAGGCCAAGGAG[C/G]CCGGATCACTTGAGG | 1161 |
rs535766968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880984 | TCTGTTTTTTCCCCA[G/T]CTTTGTGGTTTTATC | 1161 |
rs535802134 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915324 | TGGGAGAGATTCTGC[A/G]TTATGTTATCCTCCT | 1161 |
rs535939257 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900544 | TTTATTTAATTTTTT[A/T]AAAAAAATATACACA | 1161 |
rs536014439 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907319 | TTCCACTTATCCTTT[G/T]TCCTTCTTCACTCCT | 1161 |
rs536016249 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877254 | ATCTCTGTTTTGGTA[A/C]CAGTACCGTGCTGTT | 1161 |
rs536046542 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880025 | TTCCTTTCCATGTTT[A/G]GTGCTTCCTTCAGGA | 1161 |
rs536053265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900715 | GTATGAGGATTTAAG[G/T]CTCTTCTGAAACAGA | 1161 |
rs536106967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875188 | CAAGCTGAATAATAC[C/T]ATTTTTAGTCCAAAA | 1161 |
rs536134017 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919270 | GGTGGATGGGTGGGA[A/G]GTAGAGATGAAACAA | 1161 |
rs536151829 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878884 | TCAGTTCTGCTCTGA[C/T]CTTAGTTATTTCTTA | 1161 |
rs536201996 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896446 | TGATCTCCTGACCTC[A/G]TGATCCACCCACCTC | 1161 |
rs536290527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939715 | TGCCCAGGCTGGTCT[C/T]GAACACCTGAGCTCA | 1161 |
rs536331611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897456 | CAAATTAAATGCTAA[C/T]TATTATTAGCACAGT | 1161 |
rs536342718 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899413 | CTTTTGAAAATTTGG[A/G]GGCAAATGAAACTGC | 1161 |
rs536352967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933545 | ATCTACTATATATTA[C/T]TTAGTTTTTGTTTTA | 1161 |
rs536390505 | snp | C/T | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898023 | TATTTTTCTCTACTA[C/T]GCTTTGCACTCCCAT | 1161 |
rs536410404 | snp | G/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918852 | TCAAGGAACTTATTC[G/T]ATGACCAAAGAATGC | 1161 |
rs536439502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878088 | TAGCATGAAGGTTGT[C/T]GAATTTTGTCAAACG | 1161 |
rs536453617 | snp | C/T | | | intron-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60924344 | TTGAATGATTTCATT[C/T]TCTGGTTGATTCCTA | 1161 |
rs536460781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910907 | GTACAATGTTGAACA[C/G]AGGAAATAATGAGGA | 1161 |
rs536463212 | snp | A/G | 8.27643e-05 | 0.00643236 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902426 | TAACTTCAAAAGCAA[A/G]TAAGTTAAATTTTAC | 1161 |
rs536472314 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915996 | GAGCCTGGGTGTTTT[C/T]CTAGGCCCCCTTCTA | 1161 |
rs536501076 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878507 | ATCTGGTCCTGGACT[C/T]TTTTTGGTTGGTAAG | 1161 |
rs536525482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60903287 | CTGAGAAAAAATGTA[C/G]CTAAATATTAAGAAC | 1161 |
rs536534765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911751 | AGTCTTTAATCCATC[C/T]TGAATTAATTTTTGT | 1161 |
rs536633209 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945835 | CCAGAGCTGAGTGGT[A/G]TAATTGAAGAGGAGT | 1161 |
rs536658178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885089 | GCAATTGTGGCTCAC[C/T]GTAGCCTTGAACTCT | 1161 |
rs536689598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932702 | ATCACAGTCATGAGT[A/C]ATTGAGTCATAATTA | 1161 |
rs536721236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886053 | ACTTAAAGAACTATA[G/T]GTATATATATATGTA | 1161 |
rs536721469 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880162 | AATTCTGGGTTGAAA[A/C]TTCTTCTCTTTAAGA | 1161 |
rs536727635 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912577 | TCCTAATTGAATACC[C/T]TTTATCTCTTTCTCT | 1161 |
rs536800576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906710 | CTACAGCCTGGGCAA[C/T]GGAGCAAAACTCTGT | 1161 |
rs536864859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899197 | GAATTAAATTCTACT[A/G]TAAAAATGCAGTTTA | 1161 |
rs536932453 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937354 | GGGCAGGCCGATAGA[A/G]CTCCCAGGAGATTAT | 1161 |
rs536933906 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923587 | GATATTCTTGAAATG[C/T]GCAAATATTTCAGGT | 1161 |
rs536966990 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946335 | ATATAAGATCAGCAA[C/T]GTTGAGAAGCACTAA | 1161 |
rs537020465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943734 | GGGAACATGCTGATT[A/G]TGGCAACAATGACAC | 1161 |
rs537044647 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873685 | CCATCTCAGGAAAAA[A/C]ACAAAAAAACAAAAA | 1161 |
rs537108408 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874352 | ACAACTGAGGTACAA[C/T]GACTTGTGTTACTTG | 1161 |
rs537118851 | snp | C/T | 0.00795532 | 0.062565 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873445 | TTTGAGAGGCCGAGG[C/T]GGGTGGATCATTTGA | 1161 |
rs537152530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929803 | ATGCCTAGTACATTG[C/T]AAGTATCTAGCGAAT | 1161 |
rs537184998 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880590 | TTTTTCTCTAAACTT[C/T]TCTTCTCACTTCATT | 1161 |
rs537191450 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934051 | TTATAAACATGCATG[C/T]GTGAGTATCTTTTTT | 1161 |
rs537225316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941325 | ATTGGAGATGGCAGA[A/G]GAAAAAATCTGTGAA | 1161 |
rs537262406 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927861 | AAGATGTTTCTCATA[C/T]ACTAGTAGATGAGAC | 1161 |
rs537265392 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883837 | GCTTTTAGAAAGGAG[A/G]GTCAAAAGGAAGCCA | 1161 |
rs537285965 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935051 | TTGGCTATGCAGGCT[A/C]TTTTTTCCTAGTTCT | 1161 |
rs537368621 | in-del | -/AAAAAT | 0.0836948 | 0.186662 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886710 | CCATCTCAAAAAAAT[-/AAAAAT]AAAAATAAAAATAAA | 1161 |
rs537406725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920151 | TTCCTGTGGTGTGAC[C/G]CTGACTGTGTTCTCT | 1161 |
rs537440790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877145 | ATAGGGAATCCTTTC[C/T]CCATTTCTTGTTTTT | 1161 |
rs537451492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879596 | AGTTAGCTCTTCTTG[C/T]TGAATTGATCCCTTT | 1161 |
rs537468028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920967 | GGAAGAGAGTATATA[C/T]GGCCTAAGTCTCTAA | 1161 |
rs537537014 | snp | A/C/T | 0.000747293 | 0.0193157 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945456 | GGGAAAAGTGAGAGC[A/C/T]CCTAGTCAACTAACG | 1161 |
rs537643488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891983 | GGAGGGCAGACATCA[C/T]GGAATCAGACAGCTC | 1161 |
rs537658895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896134 | GGAATTACAGGCATG[C/T]GCCACCATGCCCGGC | 1161 |
rs537688724 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939070 | GAAATCAGCCTGTTC[A/T]CCTTTGTTATGACAT | 1161 |
rs537751022 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932440 | GTCTGGAATTTTGGT[A/T]CATGCTAGATAGAGG | 1161 |
rs537786343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884245 | AGGACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 1161 |
rs537867904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917883 | ATAAATCCAATTTTC[C/T]ACTTTAGATTACTAG | 1161 |
rs537929274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918536 | AGCTGTGTAGAAGGC[A/G]AGAAAGAATGTCCAG | 1161 |
rs537931099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910984 | TTGCTTTAGTTTTTT[A/T]AAAAAATAGATACTT | 1161 |
rs537961143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938393 | GGAGTCTCGCTCTGT[C/T]GCCAGGCTGGAGTGC | 1161 |
rs538014812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922500 | TGACTATGCTAAATA[A/C]AAAAGGAATTAGACA | 1161 |
rs538037419 | snp | G/T | 5.06693e-05 | 0.0050331 | upstream-variant-2KB, synonymous-codon | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945312 | GCTGTCAAGGGAAGT[G/T]AAGGAGCACGTGGGC | 1161 |
rs538041309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887673 | TGCTGTTTTTCCTTT[A/G]TTTCTTTGTTAGTAA | 1161 |
rs538078408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915449 | AATTTTCTACTGATG[C/T]AGTAAGGAAAGTACT | 1161 |
rs538101168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944859 | GATGAGACGGGAAAG[C/T]GTGGGGCAAAGCTTA | 1161 |
rs538102626 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888591 | TTAAATTAGAATGAC[G/T]AACAAAGAACACTTA | 1161 |
rs538140818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924077 | CCTGTACTTTTCCCC[A/T]CTCTTGTAATTTATT | 1161 |
rs538142142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60916106 | CTTCATTTCTTAAGT[C/T]TATGGTCTCGCATAG | 1161 |
rs538263445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906427 | TTTGGAGAAGGGCTA[C/T]TATCATTTAAACTAT | 1161 |
rs538357218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942078 | ATTTTATAATTCCTA[A/G]AGCAGCCACTAAAGA | 1161 |
rs538383560 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894899 | ATTTGTCGGCTGGGC[A/G]TGGTCTCACTCCCGT | 1161 |
rs538444907 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930882 | GAGGCCAAGGAGGCC[A/G]GATCACTTGAGGTCA | 1161 |
rs538652236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890471 | GTATTAACTTCAAAA[C/T]CTCCCTTTACTAGCC | 1161 |
rs538654386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882120 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 1161 |
rs538790657 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878550 | GCCTCAATTTCAGAG[A/C]CTGTTATTGGTCTAT | 1161 |
rs538822898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879028 | TAAATTGCCCTCTAC[A/G]CACTGCTTTGAATGT | 1161 |
rs538852103 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882834 | TGGGTTGTCAATTTG[A/C]CTATTAAATTAGGTT | 1161 |
rs538944854 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896517 | GCCTGGCCTGTCAAC[C/T]TTAAAATAAAAAAAA | 1161 |
rs538965834 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898135 | TGAGTTGAGAATTAC[C/T]AGTCCACATAGTAGA | 1161 |
rs538995667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933647 | AGTTCTTCAGTGGTG[A/G]TTTCTGAGATTTTGG | 1161 |
rs539008692 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940513 | ACAGGGAGTCCCAGA[G/T]AACTGGGAAGCATCC | 1161 |
rs539048193 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934375 | TTGTTGGCCATTTGT[A/G]TATCTTCTTTTGAGA | 1161 |
rs539053521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944467 | ATCTCTTGTCAATGG[C/T]CCCTACCCCAATTCT | 1161 |
rs539101999 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893749 | ACTGGGCAGTCTCCA[C/T]GAGGGGGCGGGGCTT | 1161 |
rs539190673 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911512 | TGTCAGATGGGTAGA[A/T]TGCAAAAATTTTCTC | 1161 |
rs539378785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886195 | CCTTTAAACAGCCTC[C/T]ATCTTCCTACTGCTT | 1161 |
rs539382609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894142 | GGCGACCGCCACCAC[A/G]CCCGGCTAATTTTTT | 1161 |
rs539412453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938192 | CTTGATTTCCAACTT[A/G]TAACTTCAATTTTCA | 1161 |
rs539436940 | in-del | -/A | 0.45762 | 0.139261 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938090 | ATATATATATATTTT[-/A]TTTTTTTTTTTTTTA | 1161 |
rs539473272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930783 | ACAGTAATGAGTTAT[C/G]TGACTTTGATCAATA | 1161 |
rs539514331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923457 | AAATCATCTTTAAAT[A/C]TGGAGTTGTTGACAC | 1161 |
rs539536455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876341 | GCCGCAATAAACATA[C/T]GTGTGCATGTGTCTT | 1161 |
rs539548460 | in-del | -/TTTA | 0.000205929 | 0.010145 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922189 | ACATTAATTTATCAT[-/TTTA]TTTATTATTTAGTCC | 1161 |
rs539617582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935939 | GCTGGATTTGGTTAG[C/G]AAGTATTTTGTTGGG | 1161 |
rs539659212 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879174 | TTCCATGTAGTTGAG[C/T]GGTTTTGAGTGAGTT | 1161 |
rs539715017 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879673 | GTCTGTTTTATCAGA[C/G]ACTAGGATTACAACC | 1161 |
rs539753850 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937748 | GCCAACTCACAGTTC[C/T]TTGGCTGTCCCACAG | 1161 |
rs539796095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892068 | TAGAGCCTGGCCCTG[C/T]TGTAGGGGGTCCATC | 1161 |
rs539817407 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875133 | GGATGAAAATAACTT[C/T]TATAAATAAACAAAT | 1161 |
rs539923255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915280 | TTGGAAGTTTCTGTT[C/T]TGAGTGCTAGAAATT | 1161 |
rs539970581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939465 | TTGTTTGGATTCCCC[A/G]GTTGCAATACTTCTT | 1161 |
rs539974558 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881377 | GGAGAACCACTATTC[C/T]CTTCAAAGCTGTCAG | 1161 |
rs540037762 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910320 | CTTGATATCTGATAG[A/T]GAAGTCTTCCAACTT | 1161 |
rs540087575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917341 | TAGTTGCAGCAAAGC[A/G]TTTGTGTTGAAAACT | 1161 |
rs540099811 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945985 | TCCCCACAAGGCTCG[C/T]TGATTCCTTTCTCGG | 1161 |
rs540126251 | snp | C/G | 1.65012e-05 | 0.00287234 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928894 | GGTTCAATGTCAAGG[C/G]TGTTAATTCCACCGC | 1161 |
rs540168263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879996 | CATGTTTTTGCAGTG[G/T]CTGGTACCGGTTGTT | 1161 |
rs540195024 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902663 | ATAATCGATGTTTCA[A/T]TGCTAATGTGAAGTT | 1161 |
rs540275984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930954 | TCTACTAAAAATACA[A/G]AAAAATTAGCCAGGT | 1161 |
rs540287160 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920591 | ATAGTCTTTATTGAA[A/G]TTATTTTTAAATTGG | 1161 |
rs540336849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931824 | TATAAAGGTAATCAT[C/T]TTTTCCTTCAGCTCC | 1161 |
rs540393830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916528 | GTGCTGGTTTGGCTA[C/T]AAGATATTCCATTAT | 1161 |
rs540507745 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901601 | TCTCTGCCAAAGCTA[A/C]AAAGTTAACTGTATT | 1161 |
rs540528689 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945518 | GAATTTCCCGAGTTC[C/G]TTCTCCCCTGTCGAC | 1161 |
rs540542618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937917 | TGCCAAGTTAGTCCT[A/G]CCTCCTATACACCAT | 1161 |
rs540603470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935157 | CAATATTGATTCTAC[A/C]CATCCAAATGTAGAA | 1161 |
rs540608260 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894829 | TTGGGAATCATGATC[A/T]TGCATATCAACAAAA | 1161 |
rs540616479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894298 | TGGGAATTTATCTTA[A/G]GGAAATAATTAAATA | 1161 |
rs540666612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944187 | CCACTCAATTTCCAT[A/G]GCCTGTTGATTCTAT | 1161 |
rs540729035 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923707 | TATGTCTCTTTTGGA[A/G]GTTACACCAAATTTA | 1161 |
rs540730134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928297 | GTGGCAGCAGTGGTG[A/G]CAACTGTTTATGACG | 1161 |
rs540751313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876463 | TTCCTACATGGACTT[A/C]CACAATGGTTGAACT | 1161 |
rs540759295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881406 | AGACAGGGACATTTA[A/T]GTCTGCAGAGGTTTC | 1161 |
rs540773259 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935354 | GTCACTGTTGGTGTA[C/T]AGCAGAGCTACTGAC | 1161 |
rs540774472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920368 | AAATTTTTAATGTAG[C/T]GATAACAAATAAAAG | 1161 |
rs540789025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905200 | GATGATGTAGCCAGC[A/G]CTGCCTCTCAGTTCC | 1161 |
rs540824852 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891345 | CAGACTTCAACCTTG[A/T]AGAATCATTTTAGAC | 1161 |
rs540845225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900776 | TGATTACTAGGTCCA[C/T]TGTGGTACTGATTCA | 1161 |
rs540906591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893827 | ATTTACCATCATAAC[C/G]ATTTTTAATGGTACT | 1161 |
rs540944495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934759 | GGTGAGAGATGAAGA[C/T]CCATTTTCATTTTCC | 1161 |
rs541090247 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879253 | TTGCTATAATTTCTG[A/T]TCTTTTACATTTGCT | 1161 |
rs541095079 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912073 | TTGTCTTGGTAATGC[A/G]GGCTCTTTTTTGGTT | 1161 |
rs541116187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904696 | TATAAAATTGTGATA[C/T]TCCTCTGGGTTAAAA | 1161 |
rs541214378 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916652 | AAAATAAATCTGAAA[C/T]AATAGGACTATTCTA | 1161 |
rs541227735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881816 | TGCTTCCCAGGTGAG[A/G]CGATGCCTCACCCTG | 1161 |
rs541232547 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938127 | GAAGTTTCATTGAAT[A/G]TAAGTTTCTCTGGGT | 1161 |
rs541291712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882136 | GTGAGCCACTGCGCC[C/T]GGCTTAGAAACATTT | 1161 |
rs541353138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878176 | GCTCGATTACGTTTA[C/T]TGATTTGTGTATGTT | 1161 |
rs541449851 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919355 | ACTCTCCAATCTTGT[A/G]TATGTTTGAAATTTC | 1161 |
rs541513101 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912731 | TTGGCTGTGGGTTTG[C/T]CATAAATAGCCCTTA | 1161 |
rs541514660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900956 | GCTACATTCTAGACC[G/T]TGCTGCACTTCAGAA | 1161 |
rs541594875 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940080 | CTAGATCTTTTGAAT[A/C]TACCCTCCTAATCTC | 1161 |
rs541623529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889881 | AAATGGGATATACCT[C/T]CTTATTGACTAATAA | 1161 |
rs541674964 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943380 | CCACAGTTTATTAAC[C/T]GTGAGAAATAGCATA | 1161 |
rs541685388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880751 | CTGCATTGGTTATTC[C/T]AGTTAGCCATTTGTC | 1161 |
rs541748905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876015 | GTATATCTCCTAATG[C/T]TATCCCTCCCCCCTA | 1161 |
rs541771971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915657 | GAGACCACCCACATT[C/T]CTTGGCTTGTGATCC | 1161 |
rs541835450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908763 | AAGTGTGCAGCTGTG[A/G]TTGCCCACCATTTCA | 1161 |
rs541848400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942653 | AGCAGAGAAAGAAGG[C/G]AGACAGGGATTATAA | 1161 |
rs541915302 | in-del | -/T | 0.438946 | 0.163706 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891662 | TGGGGGGGCATATTC[-/T]TTTTTTTTTTTTCCT | 1161 |
rs541933632 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900863 | AAACCAAGTTAAGCA[G/T]GAAAAATGTAAAATC | 1161 |
rs541957935 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931041 | TTGAACTCAGGGGAC[A/G]GAGGTTGCAGTGAGC | 1161 |
rs541995277 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898020 | TTTTATTTTTCTCTA[C/G]TACGCTTTGCACTCC | 1161 |
rs542021897 | in-del | -/TT | 0.00676609 | 0.0577691 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926312 | TTCACTGAGAATGTC[-/TT]GTTACAAACATGTCT | 1161 |
rs542022094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913771 | TGCTTTAAATGTGTC[C/T]CAGAGATTCTGGTAC | 1161 |
rs542150700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922918 | AGTTTGGAAATTCAG[G/T]AGCAGTTTCCCTGAT | 1161 |
rs542161386 | in-del | -/CC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889538 | TGGAACTCCTGGGCT[-/CC]CAAGTGATGCTTTCG | 1161 |
rs542195582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899442 | GCCATTTTTATTTGT[A/G]TCTTAAAGAAAGAGA | 1161 |
rs542197403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907902 | TACTGTAAATCACAC[A/T]ATTCTTCCAATATTA | 1161 |
rs542202272 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60874877 | AATGTAACTTCATTT[G/T]AAACAGACAACACCA | 1161 |
rs542258139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899848 | ACATATGTATTCATA[C/T]ATTAGGGTTGTTGAA | 1161 |
rs542285699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893328 | CCTGGCGTCTTAGGA[C/T]ATCCTCACAGTAGCT | 1161 |
rs542308826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940109 | TCTTATCATTTTCAT[C/T]ACTGGTCTTTTAATT | 1161 |
rs542324545 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937356 | GCAGGCCGATAGAGC[C/T]CCCAGGAGATTATGT | 1161 |
rs542375605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918203 | TAATCATACTAAAAT[C/G]GTTTAGGATTAAATT | 1161 |
rs542437001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914307 | TATTTAGGATAGGTA[G/T]CTCTTCTTGTTGTGA | 1161 |
rs542464903 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875750 | CGCCCGGGCTGGAGT[A/G]CAGTGGCGCGATCTC | 1161 |
rs542488548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911177 | TAACTCATCATTTAC[A/G]TTAGGTATTTCTCCT | 1161 |
rs542550501 | snp | A/G | 7.08366e-05 | 0.00595091 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903556 | CAAAGTACATTAGTC[A/G]TGTCACTTACAAAGA | 1161 |
rs542560062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904281 | GTAGAGACTCACATG[A/G]TGCCAAAGAAATAAT | 1161 |
rs542634320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931909 | TACCAATATATTTAT[C/T]AATCCCCTGTATGTA | 1161 |
rs542659281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896824 | ATGGAATAGAACCAC[A/G]TGAACAATTTATATA | 1161 |
rs542659650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889268 | ATATGTTGAGATTAT[A/T]TAAATATCTCATTCC | 1161 |
rs542713219 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925203 | AAACATCCTCTTCTT[A/C/T]CCTTAAAAATTTTTT | 1161 |
rs542722701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889971 | GTTAAGGTGACGTCT[A/G]AGAGGTCCCAGGGAA | 1161 |
rs542744150 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886007 | TTAAGATTACCTTAA[G/T]GTGTTTCCAACTACA | 1161 |
rs542774871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910458 | TGCATTGATTCTATA[A/G]ATCAGTTTGGGTAGA | 1161 |
rs542814257 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910040 | TGTTAATTGACTGTT[G/T]ATGTAATCCAGAAGG | 1161 |
rs542827563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894355 | CTATCCAGTATTATT[G/T]AGAATGGGGTAATAA | 1161 |
rs542862042 | in-del | -/G/TTG | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884534 | TGTGTTTTTTTTTTT[-/G/TTG]TTTGTTTTCTAGTGT | 1161 |
rs542888926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895103 | TGAACCTGGGAGGTG[A/G]AGGCTGCAGTGAGCC | 1161 |
rs543035858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908484 | CATTCCAACCCTTCC[C/T]CATCTTACTAAATAA | 1161 |
rs543048581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921238 | CCAACAAACAATAGC[A/T]AATCTCCTCCGAAAT | 1161 |
rs543071611 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878093 | TGAAGGTTGTTGAAT[G/T]TTGTCAAACGCCTTT | 1161 |
rs543117619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921933 | GAACAGCCATGCAAA[C/T]GTGTTATGTGAACCA | 1161 |
rs543118683 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876843 | GTTGCTTGTTCACTC[A/T]GATGGTAGTTTCTTT | 1161 |
rs543179737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877289 | TTACTGTAGCCTTGT[A/G]GTATAGTTTGAAGTC | 1161 |
rs543222037 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931962 | CATCCCCTCCCCCAA[A/C]AGCTTGGGCTCTGAT | 1161 |
rs543227882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933805 | AGCTCAGCTCCCACT[C/T]ATGAGTGAGAACATA | 1161 |
rs543230237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892291 | CATCGGAGAATGGAG[A/C]AACTTGATCTCCATT | 1161 |
rs543291626 | snp | C/G | 0.000873024 | 0.0208746 | missense | ERCC8 | GRCh38.p7 | 5:60887457 | CATCATCATCAGGAA[C/G]TGGTTCATATAAGGA | 1161 |
rs543316851 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907921 | CTTCCAATATTACCA[A/G]TATGTTCCTCATCTG | 1161 |
rs543352993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881192 | ATATTGGTGAATAGC[A/C]AATGTTGCTAGCTGA | 1161 |
rs543354780 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904518 | AAAAGGAACTCTTTA[A/G]ACAGAAATACGCTCT | 1161 |
rs543358381 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934646 | CTTTGCCTAGGCCAA[A/T]GTCTAGAAGGGTTTT | 1161 |
rs543363620 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879274 | TACATTTGCTGAGGA[C/G]AGCTTTACTTCCAAC | 1161 |
rs543398732 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879376 | GAGTTCTGTAGATGT[C/G]TATTAGGTCTGCTTG | 1161 |
rs543414511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879807 | ACACTGATGGGTCTT[C/G]ACTCTTTATCCAATT | 1161 |
rs543419274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912799 | GAGAGTTTTTGGCAT[A/G]AAGGGCTGTTGCATT | 1161 |
rs543501775 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897920 | AACATTTCAGATTTC[A/T]GATTTTCAGATTAGG | 1161 |
rs543517781 | snp | C/T | 3.3561e-05 | 0.00409626 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60874657 | GGCATCTTCAAAGGC[C/T]GGATTTAATTGTGAT | 1161 |
rs543578855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875236 | GTAGTGATATTTATG[G/T]ACTTATTTGTAAGCA | 1161 |
rs543665493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878330 | TATTGGTGTAAAATT[C/T]TCTTTTTTTGTTGTG | 1161 |
rs543690877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942326 | AGAGAAATAAAAGCA[C/T]ATGTTCATACAATGA | 1161 |
rs543711856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936214 | GTTGCTGGTCTGTCC[A/G]GGGTTTCTATTTTTT | 1161 |
rs543801373 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929364 | GCTTTGGGAGGCTGA[A/G]GTGAGAAGACTCCCT | 1161 |
rs543806770 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939942 | TATACATACTTTTAT[G/T]TCTTTTTTATCAATC | 1161 |
rs543828821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913422 | TAGTTTGTATTTCTG[G/T]GGGATTGGTGGTGAT | 1161 |
rs543892777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906131 | ATATCTTGTGCCTCC[A/G]GAATAATGGCTGGCA | 1161 |
rs543918118 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914187 | TCTAATGTTGAGAGT[G/T]GGGTGTTAAAGTCTC | 1161 |
rs543918215 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883192 | AAAATCATAATCAGT[C/T]GCATACAAATTATTT | 1161 |
rs543955758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902566 | AAATCAGAAGATAAA[A/G]TGCCAATAATTTTGC | 1161 |
rs543977474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911656 | TGTTTTAGACATGAA[A/G]TCCTTGCCCATACCT | 1161 |
rs544005329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882978 | CTGGGAAAACACACA[C/T]ACACACACACACACA | 1161 |
rs544008521 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926114 | ACAGGTGTGAGCCAC[C/T]GCACCCGGCCTGTCA | 1161 |
rs544050972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930917 | TTCAAGATCAGCCTG[A/G]CCAACATGGTGAAAC | 1161 |
rs544066182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878706 | TATTTCTGTGGGATT[A/G]GTGGTGATATCCCCT | 1161 |
rs544085706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881026 | TTTGATGATGGTGAC[A/G]TACAGATGGGGTTTT | 1161 |
rs544111980 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923635 | CCTTAATTCAAAGTA[A/C]CTTTCTTTAGTATAC | 1161 |
rs544148845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876392 | TCCTTTGGGTATATA[C/T]CCAGTAATGGGATGG | 1161 |
rs544263367 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895373 | CATTTAGCTACCTCA[C/T]GGCAGTAGCAGTATA | 1161 |
rs544264967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937508 | ATGGTTCCCAGGCCA[A/G]TGGAGTTATGTTCCC | 1161 |
rs544353214 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924638 | ATTTATTCTGCTCTT[C/T]TGCCTTGGTTTCTTT | 1161 |
rs544393002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923010 | ACAATCCAAGCCCAT[C/T]CTAGGAACCAAAAGA | 1161 |
rs544398381 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945488 | ATCATGCGACACTTA[C/G]GGTGTCACCGGAGAG | 1161 |
rs544452437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915740 | AGTCAAATTTACCCC[A/G]TCTCCTTCTGCCTCC | 1161 |
rs544464328 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927976 | TAAAATAAAAATTCT[-/G]GGGGAAATGCTAAAC | 1161 |
rs544515914 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916382 | GAAAAAGAGTGTGTG[C/G]AAAGTTGAATGCATT | 1161 |
rs544518425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944045 | AATGTGGGCAAAATT[A/G]AAAGTACAACTTGCT | 1161 |
rs544526701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943321 | ATTTGTCTTAAACGT[A/G]TAAGCAATCCTCACT | 1161 |
rs544543358 | snp | C/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945914 | TGGCACCCTGGCTCC[C/G]GCGCTGGCCCCATGC | 1161 |
rs544572947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893363 | ATAGACCTGCGTTTT[C/T]GTCTTTCTTGCTCCT | 1161 |
rs544588143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940767 | CAGTCCATAAGTAGG[C/T]AGGTTCTTGTAGCCT | 1161 |
rs544588240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934137 | AATGGTAGTACTACT[C/T]TTAGTTCTTTAAGGA | 1161 |
rs544634685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893766 | AGGGGGCGGGGCTTC[C/T]CCCTTCCCTTTATAG | 1161 |
rs544642098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937858 | TATAGCAAAAGTTCA[C/T]GATATGCATCTCCAT | 1161 |
rs544649531 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934677 | ATCAATGTTATCTTC[C/T]AGAATTTTTATGGCT | 1161 |
rs544712537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935116 | ATTGAATTTGTAGAT[A/T]GTTTTTGGCAGTATG | 1161 |
rs544738179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880808 | CTTTGCCATGGGTTC[A/G]AACTTCCTCCTTTAG | 1161 |
rs544819596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908039 | TCCTGATTTTCCTCT[C/T]TCTCTCCTTGGCTAC | 1161 |
rs544897505 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904668 | TATATATATATATAT[A/G]TATATATATATATAT | 1161 |
rs544922848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940200 | TCTGGGTAATACTAC[C/T]ATAAAAACTAAACAA | 1161 |
rs545008323 | snp | A/C | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919345 | TCATTATACAACTCT[A/C]CAATCTTGTATATGT | 1161 |
rs545028930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891176 | CTTAAAATATTATGC[C/T]ATAAAAAGGGCTCTT | 1161 |
rs545036754 | snp | G/T | 1.65616e-05 | 0.00287759 | stop-gained, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918314 | TTATCAAATGAGCTT[G/T]ATGTGAACATGCCAG | 1161 |
rs545049313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925367 | TTCCAGCAGTTTTCC[C/T]CAGTATATAGTTCTG | 1161 |
rs545058825 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916546 | GATATTCCATTATAG[C/T]CAGAAGTGAAAGGTC | 1161 |
rs545079299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877468 | AATTACCTTGGGCAG[C/T]ATGGCCATTTTCACA | 1161 |
rs545095190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911354 | GATGACGAGTGATGA[C/T]GAGATTTTTTCATGT | 1161 |
rs545189230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943620 | GATTAAAAGAGGAAA[C/T]TGGCCAAAAGAATGA | 1161 |
rs545193114 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911533 | AAATTTTCTCCCATT[C/G]TGTAGGTTGCATGTT | 1161 |
rs545212876 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890354 | ATTTGTGCAAATGTT[C/T]TCTGAAAAAATGAAA | 1161 |
rs545262974 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917174 | TCTAAAGCAACAAAT[C/T]TCATAAGTGGCAGAA | 1161 |
rs545322964 | snp | A/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946063 | AATAATCATGGTGTT[A/G]CTGTGTAGGATTCGT | 1161 |
rs545327000 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908803 | AGTCCAGCATAAGAA[C/T]CATTATGAAAAAAGA | 1161 |
rs545328390 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882234 | AATCTTAGAATTCAA[A/T]CAATGAAAACAGTAG | 1161 |
rs545339198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881804 | CCTGACCCCTTGTGC[C/T]TCCCAGGTGAGGCGA | 1161 |
rs545366441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890048 | TACCAGCCAGTAGGA[C/T]ATATAAATATTTATA | 1161 |
rs545421602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925914 | CTGCAACCTCTGCCT[C/T]CCAGGTTCAAGTGAT | 1161 |
rs545430881 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914955 | ACTCATGATATATTA[A/T]TCTTTTTGTATGTTG | 1161 |
rs545481887 | snp | A/G | 0.00364888 | 0.0425573 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901111 | ATATGAATAGCTTTC[A/G]TAATAATTCTTCTTC | 1161 |
rs545494245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915565 | CTCACATAGGTCTCA[A/G]TGGATTATAATCAAG | 1161 |
rs545534854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875887 | ATTTTAATTTATTTA[C/T]TTTTTCTTTTTTTTA | 1161 |
rs545565172 | snp | C/T | | | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903390 | TTTTTAATGTAGAAA[C/T]AACACAAGGTTTTGA | 1161 |
rs545596910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884408 | GTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAAC | 1161 |
rs545603307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938872 | CTTACCTTACCTAAT[A/G]TTCGTAGTGATGTCC | 1161 |
rs545618808 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876106 | ACTGTTCAATTCCCA[C/T]CTATGAGTGAGAACT | 1161 |
rs545632302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931981 | TTGGGCTCTGATTTC[C/T]GTCTCCTCTAAAATC | 1161 |
rs545658200 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879871 | CCCATTTACATTTAA[A/G]GTTAATATTGTTATG | 1161 |
rs545664606 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939388 | ATTTTTTTCCTGAAG[C/G]GAAATTGGGTAAAAT | 1161 |
rs545665253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881561 | AGCCTCAGCAATGGC[A/G]GGCGCCCCTCCCCCA | 1161 |
rs545686341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893251 | CTTCATAGTGGCCTC[A/G]TCATCCAGCTGAGGA | 1161 |
rs545695729 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60924441 | GTATCTGAAATCAGT[A/T]TGGCTGGATATAAAA | 1161 |
rs545723332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880257 | GTCTGATGGGGTTCC[A/G]TTTGTGGGTAACCCG | 1161 |
rs545728652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876905 | TCCCATTTGTCAATT[C/T]TGGCTTTTGTTGCCA | 1161 |
rs545945689 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909141 | AAGCTTCTGCCCACC[-/A]AAAGGCAGCAGATGA | 1161 |
rs546085526 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929184 | ATTTAAAGACGGAAA[C/T]TTGTACGAAAAAAGT | 1161 |
rs546176220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914233 | GGGAGTCTAAGTCTC[C/T]TTGTAGGTCTGTATG | 1161 |
rs546176330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906217 | ATTTTTGTATTTTTG[A/G]TAGAGATGGGGTTTT | 1161 |
rs546239327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906842 | AAAGCCCAGCAATAA[C/T]TAAGGCAGCTTGAAG | 1161 |
rs546239944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894579 | CTTGTACTCCAAAGG[C/T]GTAGTGTGCAGGCTC | 1161 |
rs546262962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899388 | GCAAGTTAATTCACA[A/G]AAATTTCTACTTTTG | 1161 |
rs546288522 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939686 | TTTTTAGTAGAGATG[A/G]GGTTTTGCCATGTTG | 1161 |
rs546327107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881587 | CCCCAGCCTGGCTGC[C/T]GCCTTGCAGTTTGAT | 1161 |
rs546328344 | snp | C/G/T | 1.64787e-05 | 0.00287038 | missense | ERCC8 | GRCh38.p7 | 5:60887459 | TCATCATCAGGAACT[C/G/T]GTTCATATAAGGATG | 1161 |
rs546344141 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888732 | TCCAAAAGACTTCTT[C/T]TCCCCCTTGAATCAT | 1161 |
rs546352778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927622 | ACAGGCCACACAACT[A/G]ATTACTACACCAAGT | 1161 |
rs546403769 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918482 | AGTCTCAGGTAGGAT[A/G]ATATGAATGGCCAAA | 1161 |
rs546414288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920189 | CTTCTTTTGTTTTCT[A/G]CTCATTTTCTAAGTC | 1161 |
rs546447178 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873744 | TCAAGCTCATAAAAG[C/T]CTCATTTACTAGTCT | 1161 |
rs546456432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912892 | TATGTGATGGATTAC[A/G]TGTATTGATTTGCCT | 1161 |
rs546563626 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915585 | TTATAATCAAGGTGT[C/T]GACAGGCTGCATTCC | 1161 |
rs546568350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930386 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 1161 |
rs546608709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944506 | GTCATTCTGAACTTT[A/G]TTCAATTCCTGGCCT | 1161 |
rs546609588 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938551 | TAGAGACGGGGTTTC[A/C]CCATGTTGGCCACGC | 1161 |
rs546672702 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931312 | ATTAAATTTTTTTTT[A/T]AATTTACTTTTAGAG | 1161 |
rs546681074 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894654 | AGGCCCCACCCCAAT[A/C]CTACCGAAAATAATC | 1161 |
rs546719660 | snp | A/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946551 | CAAAGAACATAGCAT[A/G]GTGTTAAGTATTTCT | 1161 |
rs546733617 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932120 | ACCTCTGCCCAACAT[A/C]ATGACTTCAGGACTG | 1161 |
rs546782094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936749 | AGTTCAAAGAATTTT[C/T]TAATTTCCATCTTGA | 1161 |
rs546843825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901306 | AATTTTCAGGCACCT[A/C]GGTACTTTCCTGTAG | 1161 |
rs546845752 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937576 | CACCAAGGAAGTTGG[C/G]GAAGGCCGGCAGCCA | 1161 |
rs546852010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909397 | GAAATACAGCAGAAC[A/G]CACAAAAATTACGAT | 1161 |
rs546866583 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944827 | GAGGGCAAATAATAG[C/T]TTGGTGGCAGGAGAG | 1161 |
rs546872986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894145 | GACCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 1161 |
rs546902072 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893479 | CTGAGGAGCAGAGGG[A/C]ACTTTGGAGGTTGCT | 1161 |
rs546952821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922257 | TTGCAAACACTCAAA[C/T]GTATTAAGGATACAT | 1161 |
rs546970014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927115 | CTTCACAGAGTGATA[C/T]GCAAATGCACCCTCT | 1161 |
rs546973404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875621 | CAATTTTATTCAGAT[G/T]CCAATTCCAATGCTG | 1161 |
rs547011790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915299 | GTGCTAGAAATTATA[C/T]AGAAAAAATTGGGAG | 1161 |
rs547018431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880860 | GAAGCCCTTTTTTCT[C/T]AACTCGTCAATGTCA | 1161 |
rs547052107 | snp | C/G | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919827 | TGGCTGTATAGTGAA[C/G]ATTTGCATTAGGTTA | 1161 |
rs547133603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893090 | AATCTTTTTCAAGAC[C/G]AGGACCAGCTTCTTG | 1161 |
rs547179598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933528 | CAGCCCCTGTATTTT[C/T]TATCTACTATATATT | 1161 |
rs547190085 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876707 | TTGTTCATATCCTTC[A/G]TCCACTTTTTGATGG | 1161 |
rs547225935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889481 | TGGCTGATTTTTTGA[C/T]TTTTTGTAAATACAG | 1161 |
rs547230227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884712 | CATGATCACATTCAT[A/G]TTCTGCCTATATTCA | 1161 |
rs547241168 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934214 | CTGGCAGTGGAAAAG[C/T]GTTCCCTTTTCACCA | 1161 |
rs547258276 | snp | A/G | 1.65395e-05 | 0.00287567 | upstream-variant-2KB, synonymous-codon | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945336 | CGTGGGCACGGACCA[A/G]TTCGGGAACAAATAC | 1161 |
rs547306505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926225 | TTGAACAAAATACAA[C/T]TAAATGTAGAGGCAG | 1161 |
rs547336101 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878379 | ATCAGGATGATGCTG[A/G]CCTCATCAAATGAGT | 1161 |
rs547352563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60902885 | ATTTCTCATAAAGTT[A/G]TAAGAGAAACCTACT | 1161 |
rs547470940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913048 | GGATATTGGTGTAAA[C/T]TTCTCTTTTTTTGTT | 1161 |
rs547479737 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873441 | GCACTTTGAGAGGCC[C/G]AGGCGGGTGGATCAT | 1161 |
rs547560824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940293 | AAATGGCTATGGCTA[C/T]GCATAGTGGCCTGCA | 1161 |
rs547562954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896309 | GCAACCTCCACCTCC[A/C]GGGTTCAAGCGATTC | 1161 |
rs547585826 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876979 | GTCCTGAATGGTAAT[C/G]CCTAGGTTTTCTTCT | 1161 |
rs547638439 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882028 | TTGTATTTTTAGTAG[A/G]GACGGGGTTTCACCG | 1161 |
rs547657325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924597 | TTATTTATCCTAGAA[A/G]AGCTTTCTTGAATTA | 1161 |
rs547687595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910815 | TCATGTCTTCTGTGA[A/G]TGACAGTTTAAATGC | 1161 |
rs547701003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882462 | TGCAGTGGCATGATC[C/T]TGGCTCTCTGCAACC | 1161 |
rs547716916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917657 | GTGATCATGTTCAGT[C/T]GGGACCATGTTAAGT | 1161 |
rs547739285 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912170 | GGTATTCAATCTATA[A/C]ATTACCTTGGGCAGT | 1161 |
rs547750449 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60899718 | CCATAATTTTACTCT[A/G]CTGTCAGCACTGAGA | 1161 |
rs547796203 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914572 | AAGGTGGGAGGATCA[-/T]TTGAGGCCAGATTTT | 1161 |
rs547840842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908350 | GTGAGGCACAAATCT[G/T]TATATTCAGTGTAGA | 1161 |
rs548055112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944329 | CTTGGCTCCCACTCT[C/T]GTTCTCAGTTGCAAC | 1161 |
rs548073037 | snp | G/T | 1.6713e-05 | 0.00289072 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918432 | AACTGACTTATGTGA[G/T]TTTCAAAACTGGTAC | 1161 |
rs548097940 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910059 | TAATCCAGAAGGCTA[C/T]CAATTAACACTAGGC | 1161 |
rs548193709 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915046 | CTGGCTTGTAATTTT[C/G]CATATAATGTCCTTG | 1161 |
rs548241090 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902676 | CAATGCTAATGTGAA[C/G]TTTACAGGGGTATTT | 1161 |
rs548247342 | in-del | -/AATGAACTATATAA | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898991 | TATGAAATATATTAG[-/AATGAACTATATAA]AACCTATGATTGTTT | 1161 |
rs548263705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879587 | ATTTAGGATAGTTAG[C/T]TCTTCTTGTTGAATT | 1161 |
rs548281099 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930205 | GAGGCTGAGGTGGGC[A/G]GATCACCTAAGGTGA | 1161 |
rs548323515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879912 | ATCCTGTCATGATGA[C/T]ATTAGCTGGTTATTT | 1161 |
rs548380028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884463 | CCTGGGTGACAGAGC[C/G]AGACTCCTTCTCAAA | 1161 |
rs548380899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921591 | ACAAGACAGGGGTGA[C/G]TGGGTATATGTGTAT | 1161 |
rs548442921 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941029 | AATGCTTGAACTTGA[G/T]CAACACTGGCATGGT | 1161 |
rs548564860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941318 | CTAACAGATTGGAGA[C/T]GGCAGAGGAAAAAAT | 1161 |
rs548651131 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877044 | CTTAATCCATCTTGA[A/G/T]TTGATTTTTGTATAA | 1161 |
rs548652488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927895 | GGTGGAAGCTGGAAG[C/T]AAAAAGTGGAAGTTT | 1161 |
rs548655899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888456 | AAGGCCAGGTAATGC[A/G]CAAGATAACTTGGTC | 1161 |
rs548669440 | snp | A/C/T | 0.000122219 | 0.00781645 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945207 | CGGCTGGAGCATTAC[A/C/T]CCTACTGCGGGTCCC | 1161 |
rs548690322 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932552 | TGTCACAATTTGTTG[C/T]TAAAGGAATAGAGTG | 1161 |
rs548713450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928769 | TAGGATTTTCATTAA[C/T]TTTAATGAAACTTCT | 1161 |
rs548713499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920830 | ATGTAGCACGTAGAA[C/T]AGGTGAAAATACTAT | 1161 |
rs548763707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905615 | TTTAGGCTTTCAGGA[A/C]CAACTACTCATCTCT | 1161 |
rs548827856 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898007 | GTAGTCCTCAGTCTT[G/T]TATTTTTCTCTACTA | 1161 |
rs548889824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941928 | TAATGTCTGATAGAG[A/T]ATATAATGTATGTAA | 1161 |
rs549014301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933300 | CTCGGCTCACTGCAA[C/G]CTCCAACTCCCAGGT | 1161 |
rs549032926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939054 | ATGCTTCTTAATGGA[A/G]GAAATCAGCCTGTTC | 1161 |
rs549047905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924813 | CTTCCATTTATTTGT[A/G]TTCTTTAAGTTTTAG | 1161 |
rs549109268 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917795 | AATGTCATACAAACT[A/C]TTATCCATTGCTTGT | 1161 |
rs549113524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925460 | GCTCCTTCTGGTCTT[A/G]CCATGGGCCACTCAA | 1161 |
rs549119844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893944 | TAAACAGCAAAGATA[A/T]TCTTACCCCTTGACC | 1161 |
rs549168412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902215 | TGACACAACACAGTT[C/G]CTCTGTGTTCTAAGG | 1161 |
rs549186090 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60873890 | GCCAGATTCCCTGCC[A/C]GGATATTTTCTGCTT | 1161 |
rs549214741 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909572 | CTTTATGATGATCCA[C/T]TTCCACTGACTTAGT | 1161 |
rs549216122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930578 | AAAAACAAAAACAAA[C/G]TAAAAAATGAGCCAG | 1161 |
rs549227876 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894791 | ATAAGCTTGGGGTGA[A/G]TGTAAAACCAGTAAC | 1161 |
rs549229815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902744 | GCTTTGGAAAAAACA[C/G]AGTTAAGTAAGTCTT | 1161 |
rs549279725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923123 | TTGGGAGTAAAAGAG[G/T]GTGCTAAAAAATTAG | 1161 |
rs549291137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895613 | AGTTCCTAGATTAAT[C/T]CCTATACATGTTTAA | 1161 |
rs549300331 | snp | A/T | 0.473359 | 0.112298 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938087 | TATATATATATATAT[A/T]TTATTTTTTTTTTTT | 1161 |
rs549314364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888064 | ATGTCAATGTCTACA[C/G]ATATGCTGTTTGCTT | 1161 |
rs549334950 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886698 | CAGATTGAGACTCCA[C/T]CTCAAAAAAATAAAA | 1161 |
rs549336841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913143 | CTTCTTTTTCTATTG[A/T]TTGGAATAGTTTCAG | 1161 |
rs549338639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920570 | CTAAGTCACATTAAC[A/T]TAATAATAGTCTTTA | 1161 |
rs549396471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880927 | TGCGTTCCTTTGGAG[C/G]AGGAGAGGTGCTCTG | 1161 |
rs549399110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908969 | ATGTAGACTCTAATA[C/T]GACTTTTAAAAAGCA | 1161 |
rs549408158 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876559 | GTTCCCTGACTTTTT[A/C]ATGATCACCATTCTA | 1161 |
rs549495143 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893921 | TCATCTTGCAAAATT[A/T]TACCCATTAAACAGC | 1161 |
rs549515428 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885933 | TTTTTGAATGTCAAA[C/T]GTGCTCTATCAATAA | 1161 |
rs549552614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926362 | TGTGTAATGATGTAG[C/T]AGATTTATGTTTTAG | 1161 |
rs549571436 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899237 | TCACATGGATTGCAG[A/C]TGACTCACATTTAAC | 1161 |
rs549580094 | in-del | -/AAAAAAAAAAAAAAAAAAAAA | 0.435407 | 0.167703 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909244 | AAATGCCCTATTCTG[-/AAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAG | 1161 |
rs549667662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882549 | ACAGGCGCATGCCAC[C/T]GGCGAATTTTTGTAT | 1161 |
rs549729430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878517 | GGACTTTTTTTGGTT[A/G]GTAAGCTATCAATGA | 1161 |
rs549747473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876148 | GGGTTTTTGTCCTTG[A/C]AATAGTTTGTTGAGA | 1161 |
rs549794552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897102 | TCCCAAGGAAGTTCT[C/T]GCCTCAGGGTCTTTG | 1161 |
rs549842780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906418 | TGGTTGAGTTTTGGA[A/G]AAGGGCTATTATCAT | 1161 |
rs549855867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890408 | TGAAAAGATCTGGAT[G/T]TAAAACAAACAAACA | 1161 |
rs549969245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883336 | AAAAATGTTGTAGAT[A/G]GATGTGGTACACATT | 1161 |
rs550144367 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873499 | GGCCAACATGGTGAA[A/T]CCCCATCTCTACTGA | 1161 |
rs550149130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911461 | TTTTCTTGTAAATTT[A/G]TTTAAGTTCTTTGTA | 1161 |
rs550160947 | in-del | -/T | 0.00480478 | 0.0487781 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935798 | CTATTGAGATAATCA[-/T]CTGATTTTTGTTTTT | 1161 |
rs550164803 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946343 | TCAGCAATGTTGAGA[A/C]GCACTAAGACCTTTC | 1161 |
rs550177574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938452 | TCTGTCTCCAGAGTT[C/G]AAGCGATTCTCCTGC | 1161 |
rs550180604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894108 | TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGGGACT | 1161 |
rs550206135 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909595 | GACTTAGTAGTAAAT[A/G]TATTTCTCTTCCTCA | 1161 |
rs550212355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903835 | AGAAATATGAAGATA[C/T]ATGCCAAAATTACAT | 1161 |
rs550304879 | snp | C/T | 9.88745e-05 | 0.00703047 | missense | ERCC8 | GRCh38.p7 | 5:60887505 | TGTTGCAGTCTCTGC[C/T]ACCACTATAAAGTTC | 1161 |
rs550344155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880915 | CTGGTGAGGAGCTGC[A/G]TTCCTTTGGAGGAGG | 1161 |
rs550375231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918513 | CCGAGATCACATGCC[C/T]GTGTCCAAGCTGTGT | 1161 |
rs550447343 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891904 | GGAACTGGTGCTTGG[A/C]TCGGAAGGGAAGTGA | 1161 |
rs550453871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912164 | GGGGATGGTATTCAA[C/T]CTATAAATTACCTTG | 1161 |
rs550486987 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935677 | TTGGCTGTGGGTTTG[C/T]TATAGATGGCTTTTA | 1161 |
rs550556668 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889220 | CAGGGTAAAATTAAT[C/G]TTTTTAGTTTGTACT | 1161 |
rs550603054 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920858 | TATTTTGCTATGTAA[C/T]AAAATAAATTTAATG | 1161 |
rs550672461 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930712 | GCCTGGGTGACATTT[A/C]TTGCAATACATCTAT | 1161 |
rs550692862 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925973 | GGATTACGGGCACGC[A/G]CCACTGCACCTGGCT | 1161 |
rs550717343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938514 | GTGTGCCACCACACC[A/C]GGCTAATTTTTGTAT | 1161 |
rs550759234 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942052 | TCCGAAGTAGACAAC[A/G]AAAAGTAAGTATTTT | 1161 |
rs550828746 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889209 | CCAGGCTCCTTCAGG[A/G]TAAAATTAATCTTTT | 1161 |
rs550840821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875545 | AGATGGTCTCATTGT[C/T]AAAGTAATTGGGTAT | 1161 |
rs550898758 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944402 | ATTCTCATCTTCACA[A/C]CTCTACTCAAGTACA | 1161 |
rs550924163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899550 | GTCAATATGCGTTTA[C/T]TATGTGGCTTCAATT | 1161 |
rs550927309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943758 | ATGACACTGCCGCCA[G/T]TTGAGACATTCTAGA | 1161 |
rs550943575 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923809 | TACATTTATCCCAAT[C/T]AAAAATAGGGGAACC | 1161 |
rs550950067 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884534 | ATGTGTTTTTTTTTT[G/T]TTTGTTTTCTAGTGT | 1161 |
rs550951086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935919 | GATTATATTTTTTAT[A/G]TGCTGCTGGATTTGG | 1161 |
rs550951774 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937082 | CAGAGCTACTGGGGT[C/G]TGGTTGGTACAGGGC | 1161 |
rs550972947 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879968 | CCTAGCCTTGATGGT[C/G]TTTACAATTTGGCAT | 1161 |
rs551014955 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941680 | AGCAACCAGAGAAAA[A/G]TGATAAATTACCTAT | 1161 |
rs551033048 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910581 | AGTTCTCTGTGTATT[C/T]GGAATAGTCTTGTAT | 1161 |
rs551073603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925499 | ACAATTAGAGTATGC[C/T]ATCTTCTCCCAGTTT | 1161 |
rs551096339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939327 | CTTTAATGTTCCTTC[A/G]GATTTCATTCAAATA | 1161 |
rs551105507 | snp | C/G | 0.000399281 | 0.0141238 | splice-acceptor-variant | ERCC8 | GRCh38.p7 | 5:60922156 | CCACCTGATAACATG[C/G]TGATAATAAAAAAGT | 1161 |
rs551111927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898767 | ATTCTATGGACTATT[A/G]AAATCAATAATTCTA | 1161 |
rs551215168 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936239 | TTTTTCCTGGTTTAA[-/T]TCTAGGAGGGTTGCG | 1161 |
rs551216096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892544 | CTCCTGACTGTGTAA[A/G]TCTCTCTTCTTCCCC | 1161 |
rs551277340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884249 | CTTTGGGAGGCCGAG[A/G]CGGGTGGATCATGAG | 1161 |
rs551280330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936591 | TTTGCTGTTTCTCCA[G/T]TTCCTTGAGGTATGC | 1161 |
rs551289587 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892927 | TGTGGGTGCGCATTT[C/T]ACCAAGGCAGCAATA | 1161 |
rs551393389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910626 | ATATTACTAGGTATA[C/T]GATGATTTTTGATGC | 1161 |
rs551400920 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926195 | GTATTTTGATTGAAA[G/T]ATTTTCATCTGATTT | 1161 |
rs551404931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933363 | AGCTGGGATTATAGG[A/C]ATCTGCCACCACACC | 1161 |
rs551462692 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919216 | ATAATTATGAATAAA[C/T]GATAGGTTGTTCGAG | 1161 |
rs551511942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911605 | TTTAATTAGATCCCA[C/T]TTGTCAATTTTGACT | 1161 |
rs551527075 | snp | C/G | 0 | 0 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945688 | TTTCCTCCCAGCCAC[C/G]CCTGTAGAGGAGCCT | 1161 |
rs551551819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912461 | CCTGAGACTTTGCTG[A/C]AGTTGCTTATCAGCT | 1161 |
rs551580143 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893427 | CCCTCTTCTTTATTT[C/T]AGCCTCTCGATTGGC | 1161 |
rs551663510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916865 | TCAGCAGTTACTGTA[C/T]ATAGCACTGAATTTA | 1161 |
rs551666306 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931302 | GAACTTTAACATTAA[A/T]TTTTTTTTTAAATTT | 1161 |
rs551679231 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881661 | GGACCCTCCGAGCCA[C/G]GCGCAGGATATAATC | 1161 |
rs551685070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889439 | GCCTCCTGCACAGCT[A/G]GGACTACAGGCATAT | 1161 |
rs551729140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906431 | GAGAAGGGCTATTAT[C/T]ATTTAAACTATAAAT | 1161 |
rs551729206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914462 | CTTCCTCCATACTTT[C/T]ATTTTGAGCCTATGT | 1161 |
rs551732331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923868 | AATGCAATCTCTCTA[C/T]ATCATCACTCTTTCC | 1161 |
rs551754702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876620 | TTGATTTGCATTTCT[C/T]TGATGGCCAGTGATG | 1161 |
rs551756567 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885503 | CCCAAAGAGCAGGAC[A/G]CAATAATTACATAAA | 1161 |
rs551788943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902333 | ACTTCATTTTAAAGG[A/C]GTGAATTAATAATTA | 1161 |
rs551923710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898986 | TAATATATGAAATAT[A/G]TTAGAATGAACTATA | 1161 |
rs551932620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923247 | CAAAAATATTTCTAA[A/G]AAGTAAAAGTAACAA | 1161 |
rs552063726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914046 | TAAGTGCAATGTGGT[A/G]CTGGGAAGAATGTAT | 1161 |
rs552070969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919920 | AGCCAAATGGGTGGA[C/T]TGTAGGGAACATGTG | 1161 |
rs552082103 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883697 | AGTTATGTATTGTGT[C/G]AATGTCAAAACAAAG | 1161 |
rs552195972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921306 | GTAATAGATAGTTGA[C/T]GTTAATGTTTACAAA | 1161 |
rs552230941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883452 | GCTTGAACATATTCA[C/T]CTATATCTCACCAGG | 1161 |
rs552249750 | snp | A/G | 1.65061e-05 | 0.00287277 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899615 | CATATTTATTAATGC[A/G]TTCTTCCTTACCTGA | 1161 |
rs552294351 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884015 | CCCCTAAGGGATTAC[A/C]TCTTGATTGATGGGG | 1161 |
rs552332298 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927844 | TAACCACATGCTAAA[A/G]TAAGATGTTTCTCAT | 1161 |
rs552373814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892392 | TGACTTGCTCGGTAT[A/C]CTCGATGTCAAAGAA | 1161 |
rs552430652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879057 | GTGTCTCAGAGATTC[C/T]GGTATGTTGTGTCTT | 1161 |
rs552483489 | in-del | -/TTAA | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911591 | CAGAAGCTCTTTAGT[-/TTAA]TTAGATCCCACTTGT | 1161 |
rs552563550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891616 | CCTTTCAAAAGAATG[A/G]TATTTTTTGGGGAGG | 1161 |
rs552597903 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935156 | GCAATATTGATTCTA[C/T]CCATCCAAATGTAGA | 1161 |
rs552598119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941252 | ACATAAATAAAAGCC[A/G]AATGGAAATTTTAGT | 1161 |
rs552626731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876342 | CCGCAATAAACATAC[A/G]TGTGCATGTGTCTTT | 1161 |
rs552725451 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935524 | TGATTTGGGTGTCCT[C/T]GATTTCTTTCTCTTG | 1161 |
rs552778595 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912268 | CCTCTTTTATTTCAT[C/T]GAGCAGTGGTTTGTA | 1161 |
rs552785495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885220 | GGTCTTTCTATGTTG[C/T]GTAGGCTGGTCTTGA | 1161 |
rs552801896 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881881 | CCTGCACCCACTGTC[C/T]GACACTCCCCAGTGA | 1161 |
rs552811193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60916274 | AGCTTTATGAAATTG[A/G]CTAAAGTCCCACTCA | 1161 |
rs552858487 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932764 | ATAAAACCTGGGGAT[A/G]GTCTTGAGGACTTCC | 1161 |
rs552903379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905430 | GATTTCAAGGTCCAA[A/T]ACCAATACCAAGGTC | 1161 |
rs552917313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893720 | TGCCAGCCTGGCGGC[G/T]CCCGACTCCGCCCAC | 1161 |
rs552922148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922802 | CATGGTTCCTGTCTT[C/T]GCAGAGTTTACAATC | 1161 |
rs552934208 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940514 | CAGGGAGTCCCAGAG[A/C]ACTGGGAAGCATCCA | 1161 |
rs552956910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875961 | TGTCACATATGTATA[C/T]ATGTGCCATGTTGGT | 1161 |
rs552989635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915597 | TGTTGACAGGCTGCA[C/T]TCCTTTTTGGAGGCT | 1161 |
rs552990423 | in-del | -/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945707 | GTAGAGGAGCCTCAG[-/T]TTTAGCCCTGGACTG | 1161 |
rs552991112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886387 | AGTGTAAACTGGTAA[A/G]ATTTGACGTGAGAAC | 1161 |
rs552995676 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930829 | ATAAAAAGCCAGGCC[A/G]GGCATGGTGGCTCAT | 1161 |
rs553061522 | in-del | -/ACAGC | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890128 | AGGTCTATATATCTT[-/ACAGC]ACAGTGTCAGGCACA | 1161 |
rs553068725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914829 | ATTGACTTTTATTTC[A/G]AAATGTTCGTATCTA | 1161 |
rs553096229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893257 | AGTGGCCTCGTCATC[C/T]AGCTGAGGAAACATA | 1161 |
rs553130437 | in-del | -/GAA | 0.0898077 | 0.191933 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938348 | GATAGCTACCTTTTT[-/GAA]TTTTTTTTTTTTTTT | 1161 |
rs553148230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890064 | ATATAAATATTTATA[C/T]ATTTTAATAATGAAT | 1161 |
rs553237027 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875513 | TGATACTCATGCAAA[G/T]AACTAAAAGGGCTTT | 1161 |
rs553269183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937773 | CCACAGTGCCTGCAG[C/T]GGCAATCCACTTCCT | 1161 |
rs553330498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930129 | CTAGACATTACATAT[A/G]GTACAACAATGACAA | 1161 |
rs553340029 | snp | C/G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60928167 | AATGCAGTGTTATGA[C/G/T]GAATTGTAAGTAGGA | 1161 |
rs553379130 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906879 | GGCAAGAGGGGGTGG[A/T]GGCTAGATCAGATCT | 1161 |
rs553406463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921789 | GTAGGTAAAGAAAAA[C/G]AAGGACATAATCACA | 1161 |
rs553444455 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907640 | TTCAGCACTGTCAGA[A/T]ATCTCACCCTATAGA | 1161 |
rs553472064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60943040 | CTTTAGGAGGCAAAG[A/G]CAGGAGGATCACTTC | 1161 |
rs553505905 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908533 | CACCCAATTGTCAAG[C/G]CAGAGAACCTGGGGG | 1161 |
rs553525229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928163 | GAGTAATGCAGTGTT[A/G]TGACGAATTGTAAGT | 1161 |
rs553538234 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925138 | ATTAATTTTCTTAAC[A/C/G]TTTTAGAATGGAGGC | 1161 |
rs553555067 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879241 | CTGAAAGACCGTTTG[C/G]TATAATTTCTGTTCT | 1161 |
rs553601591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925651 | AGTGCACAGATCTTT[C/T]AGTTGTCAGTGGTTT | 1161 |
rs553622791 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940082 | AGATCTTTTGAATCT[A/G]CCCTCCTAATCTCTT | 1161 |
rs553680676 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880004 | TGCAGTGGCTGGTAC[C/T]GGTTGTTCCTTTCCA | 1161 |
rs553709753 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946579 | TCTTGACAGGTTGCA[A/G]GCAGAGAGATGTTTC | 1161 |
rs553812551 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931838 | TCTTTTCCTTCAGCT[C/T]CCTCTTCCTAACAGT | 1161 |
rs553845587 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934106 | GTGGATACCCGGGAG[C/T]GGGAATGCTGGATCA | 1161 |
rs553846092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904122 | TTCCATTTTATCACA[C/T]CAAATCATTGTATTT | 1161 |
rs553846642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894961 | GGATCACAAGATCAG[C/G]AGTTCAACACCAGCC | 1161 |
rs553876141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932606 | AAGGATTCTTGGAAG[C/T]CTGTGCCTGGTTTCC | 1161 |
rs553905124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888055 | GCACAGCCTATGTCA[A/G]TGTCTACAGATATGC | 1161 |
rs553909445 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896716 | AAGTCCACTGTAAAA[C/T]GTATTATCCATTTTC | 1161 |
rs554047732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918622 | GGTCACAATGTGAAA[G/T]ATTCTCTGTTTTTGT | 1161 |
rs554203162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939231 | GCAGCCATATTATAT[A/G]TTTCCAGCTTGTTTA | 1161 |
rs554305696 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881457 | TGCCGTGCCCCCAGA[C/G]GTGAAGTCTACAGAG | 1161 |
rs554352832 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904944 | AAATTTTCTATTTAC[-/T]TTTTTCCTAAATTTT | 1161 |
rs554386510 | snp | A/C/T | 6.86042e-05 | 0.00585647 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898244 | ATCCATTTCTTAATT[A/C/T]ATACCCAAATATATA | 1161 |
rs554386547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906596 | TAGCTGGGCGTGGTG[A/G]CAGGCGCCTGTAATC | 1161 |
rs554395834 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877594 | GAGGTCCTTCACATC[C/T]CTTGTAAGTTGGATT | 1161 |
rs554430893 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925964 | GAGTAGCTGGGATTA[C/T]GGGCACGCGCCACTG | 1161 |
rs554447301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914062 | CTGGGAAGAATGTAT[A/G]TTCTGTTGATTTGGG | 1161 |
rs554447572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899024 | TATGATTGTTTTATA[C/T]AGTTTTTAAACTTTG | 1161 |
rs554517519 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892661 | GCACTGCAAGATGGT[A/C]TCCACTGGGGTCATG | 1161 |
rs554533579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896545 | AAAGAAGTTACTAAA[C/T]GGCAGGACTGGTTCT | 1161 |
rs554566291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879157 | GGAGGAGGTTGTTCA[A/G]TTTCCATGTAGTTGA | 1161 |
rs554583094 | snp | A/G | 0 | 0 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884349 | GGCGTGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 1161 |
rs554650469 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900884 | ATGTAAAATCCACCC[A/C]AGCATAACCAGCACC | 1161 |
rs554657075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919412 | ACTTCTGCAACCCTA[C/T]GCAGATACAACCGTG | 1161 |
rs554885437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942221 | ACTCTCACCTATTAG[C/T]GGTGGGACTGGAAAA | 1161 |
rs554901751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876360 | TGCATGTGTCTTTAT[A/G]GCAGCATGTTTTATA | 1161 |
rs554940381 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911070 | TATTTTTATATATTT[C/T]TTAATTATACTTTTA | 1161 |
rs555165360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897436 | TGCTGTCTAATACTG[A/C]CTGGCAAATTAAATG | 1161 |
rs555172729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890697 | TCAAGTTGCACAGTA[G/T]TATATTGATTCATTC | 1161 |
rs555197217 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926189 | CACTGAGTATTTTGA[C/T]TGAAAGATTTTCATC | 1161 |
rs555240472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882845 | TTTGACTATTAAATT[A/G]GGTTATTTAGTGAGA | 1161 |
rs555292201 | in-del | -/AA | 0.0134861 | 0.0810011 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941282 | TTTCAATATAAAATT[-/AA]ATTTTAACTTAATGT | 1161 |
rs555326720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934927 | CGTTGGTCTATATGC[C/T]TATTTTTATTACCAC | 1161 |
rs555368133 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880988 | TTTTTTCCCCATCTT[C/T]GTGGTTTTATCTACC | 1161 |
rs555386157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924034 | TTTAACTTTAAGCTA[C/T]AGGTCTCCTCTACCT | 1161 |
rs555413650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944036 | TCCTCAATTAATGTG[A/G]GCAAAATTAAAAGTA | 1161 |
rs555449459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917186 | AATCTCATAAGTGGC[A/G]GAATGGAACTAGAAC | 1161 |
rs555505763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944693 | AGTGTCTTCACCTGA[A/G]CCCGCGGGGGAACCC | 1161 |
rs555507593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886446 | GTGGCTCATGCGTGT[A/C]ATCCCAGCACTTTGG | 1161 |
rs555526708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921881 | TGTTAAAAAACTATA[A/C]CTGAATGTCAGTTAC | 1161 |
rs555529650 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60916059 | CAGTACCATGTGACT[C/G]GGGAAAATTGCTGTT | 1161 |
rs555569269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894218 | CTCGATCTCCTGACC[G/T]CGTGATCTGCCTGCC | 1161 |
rs555656774 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937918 | GCCAAGTTAGTCCTG[C/T]CTCCTATACACCATT | 1161 |
rs555801104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915343 | TGTTATCCTCCTCTA[C/G]AGAAGATCCAATCTC | 1161 |
rs555840728 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900545 | TTATTTAATTTTTTT[A/T]AAAAAATATACACAC | 1161 |
rs555873063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941396 | TAGAGGAAAAAAGAT[C/T]GAAGGGAAAAAGAAC | 1161 |
rs555904031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893757 | GTCTCCACGAGGGGG[C/T]GGGGCTTCTCCCTTC | 1161 |
rs555926243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918771 | TCATTCTATTAGCAC[C/T]ACTATTCTTAGAATT | 1161 |
rs555955317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880108 | TGTGAAGGATTTTAT[C/T]TCTCCTTCACTTACG | 1161 |
rs555974351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914851 | TCGTATCTATTGAGA[C/T]GACTAATATGTAGTT | 1161 |
rs555989268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919299 | AAGATTGGTTATGAT[A/G]GTTGGTGAAGCTGGG | 1161 |
rs556019108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934600 | ATCTTTGTTTTTGTC[A/G]TGTTTGCTTTTCGGT | 1161 |
rs556033826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907970 | ATTCAACACAATTGA[C/T]TACTCCCATCCTCTT | 1161 |
rs556278746 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932734 | ATGCTGAGTTCTCAG[C/T]CCTTCTAGAAAATCA | 1161 |
rs556287819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898024 | ATTTTTCTCTACTAC[A/G]CTTTGCACTCCCATT | 1161 |
rs556301109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881794 | AAGGGAATTCCCTGA[C/T]CCCTTGTGCTTCCCA | 1161 |
rs556371267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895296 | TACATGCTAATAATC[C/T]ATGGATACTATACTT | 1161 |
rs556378564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877408 | TTTTTCCAATTCTGT[A/G]AAGAAAGTCATTGGT | 1161 |
rs556556545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886059 | AGAACTATATGTATA[C/T]ATATATGTATATATA | 1161 |
rs556580770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933547 | CTACTATATATTACT[A/T]AGTTTTTGTTTTACT | 1161 |
rs556597415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921995 | TCATGTTTTGCATTC[A/G]ATGCAAAAAATACTC | 1161 |
rs556612765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939348 | CATTCAAATACATTT[A/G]GTTTTTGATTAACGT | 1161 |
rs556614678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882062 | TAGCCAGGATGATCT[C/T]GATCTCCTGATCTCG | 1161 |
rs556685577 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945447 | AGTAAAGGAGGGAAA[A/G]GTGAGAGCCCCTAGT | 1161 |
rs556689027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910912 | ATGTTGAACAGAGGA[A/G]ATAATGAGGATAATG | 1161 |
rs556750184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60903292 | AAAAAATGTACCTAA[A/T]TATTAAGAACAATGT | 1161 |
rs556772110 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892745 | TGAGCTGGGCCCTGG[A/G]ACAATGGCTGGAGCA | 1161 |
rs556789235 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877135 | CATTTACTAAATAGG[G/T]AATCCTTTCTCCATT | 1161 |
rs556793825 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932849 | GAGAGGAAAGAGTAG[A/C]CACATAAAGGAGGGA | 1161 |
rs556800134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922578 | CACCTGTCTAAGACT[C/T]AACATTTGTAAAGGA | 1161 |
rs556833451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893222 | TACCACCTCACGGAC[G/T]CCTTGTAATAAGCCT | 1161 |
rs556911986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929167 | TGCAAACTTTTAAAG[G/T]TATTTAAAGACGGAA | 1161 |
rs556932269 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880168 | GGGTTGAAAATTCTT[C/T]TCTTTAAGAATGTTG | 1161 |
rs556935749 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923383 | TACTGTTACTGTGTT[G/T]TTTTAAATGGGATTT | 1161 |
rs556991265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937671 | CTACAACAGCTCTGA[A/G]TTTATTTCCAGCAGG | 1161 |
rs556999935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875243 | TATTTATGTACTTAT[C/T]TGTAAGCAGTGATAT | 1161 |
rs557066449 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893821 | TATAAAATTTACCAT[C/T]ATAACCATTTTTAAT | 1161 |
rs557090375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899213 | TAAAAATGCAGTTTA[A/G]GTACTTTGTCACATG | 1161 |
rs557167407 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883289 | AACAATCACAAATAA[A/G]TATTATACTGGTAGT | 1161 |
rs557199854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942411 | AACTCAGATGTCCAT[C/T]GACAAGTGACTAGAT | 1161 |
rs557229045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882998 | ACACACACACACACA[C/T]ACACACATGTCTGTA | 1161 |
rs557242481 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930325 | TATTCCAGGACTTTG[A/G]GAGGCCGAGGATCAC | 1161 |
rs557263114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942999 | AATTTTAGGCTGTGT[G/T]GTAGCTCGCACATAT | 1161 |
rs557273136 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873692 | AGGAAAAAAACAAAA[A/C]AACAAAAAACCCTCA | 1161 |
rs557279729 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898878 | TTTGAGAAAGCATAA[C/T]TCTAAAATAGCCTAA | 1161 |
rs557322896 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890383 | AAAACCATCTGCTCC[A/C]TTGGTGATATGAAAA | 1161 |
rs557324529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937018 | GTTGGGGCTTCCTGA[A/G]AGCCAAACTGCAGTG | 1161 |
rs557326257 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936941 | GACTCAAGGGCTGCT[C/G]TGCAGATTCTTTTGT | 1161 |
rs557373853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920992 | CTCTAAGTTCTAGAG[C/T]ATTTGAGGCGATATC | 1161 |
rs557379747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913504 | CTTCATTAGTCTTGC[C/T]AGCAGTCTATCAGTT | 1161 |
rs557388773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928026 | TGTTTCCTTTAGTTA[A/G]TGCTATATGTGGCCT | 1161 |
rs557411211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879649 | TCTTTTGATCTTTGT[A/T]GGTTTAAAGTCTGTT | 1161 |
rs557440738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914180 | TGATCTGTCTAATGT[C/T]GAGAGTGGGGTGTTA | 1161 |
rs557464378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905701 | ACCAGGTTCTTCCTG[A/C]CTGCTGCACAAACAA | 1161 |
rs557527972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935056 | TATGCAGGCTCTTTT[C/T]TCCTAGTTCTGTGAA | 1161 |
rs557578028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903379 | TTGCATTAGTCTTTT[A/T]AATGTAGAAATAACA | 1161 |
rs557590686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927548 | GCACATATAATCTGT[A/G]ACTTCCCATATTTCT | 1161 |
rs557627018 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945971 | GAAGTAGGTCCATAT[C/T]CCCACAAGGCTCGCT | 1161 |
rs557726042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924084 | TTTTCCCCTCTCTTG[C/T]AATTTATTTGTTGCA | 1161 |
rs557748192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876789 | ATATTAGCCCTTTGT[C/T]AGATGAGTAGATTGC | 1161 |
rs557798440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938394 | GAGTCTCGCTCTGTC[A/G]CCAGGCTGGAGTGCA | 1161 |
rs557834775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911005 | ATAGATACTTTGTAT[C/G]AAATTAAGGAATTTC | 1161 |
rs557840158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901510 | TGCATCCTCATTCCT[A/G]TATTTTCAAGAGATG | 1161 |
rs557861893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938646 | GGCGTGAGCCACAGC[A/G]CCCGGCTGAATTTGT | 1161 |
rs557868343 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907677 | TCTGGGTATCTATAA[A/C]CTCTGTCCCCACTGG | 1161 |
rs557886638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881069 | CTTTCTGCTTGTTAG[G/T]TTTCCTTCTAACAGT | 1161 |
rs557917052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60915464 | CAGTAAGGAAAGTAC[A/T]TACTGTACTTAGTAA | 1161 |
rs558042174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909050 | ATCTAAAGCTGGAGA[A/G]TTGAATGCCAGATAA | 1161 |
rs558073876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877151 | AATCCTTTCTCCATT[G/T]CTTGTTTTTGTCAAG | 1161 |
rs558101479 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902794 | TAGCTTATGTCAGTA[A/T]ATCCATATAACTCAA | 1161 |
rs558197319 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935130 | TTGTTTTTGGCAGTA[C/T]GGTTATTTTCGCAAT | 1161 |
rs558213928 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928369 | TCTTCAAAACAAGCT[G/T]GTTAGGTAGGTACTA | 1161 |
rs558229326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894908 | CTGGGCGTGGTCTCA[C/T]TCCCGTAATCCCAGC | 1161 |
rs558258941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935993 | GGGATGTTGGTCTGC[C/G]GTTGTCTTTGTTCTT | 1161 |
rs558272786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887270 | ATTGCCCAGGCTGGT[A/C]TTGATTTCTGGGCTC | 1161 |
rs558303009 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939699 | TGGGGTTTTGCCATG[C/T]TGCCCAGGCTGGTCT | 1161 |
rs558308031 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912659 | GAGAGAGGGCATCCC[C/T]GTCTTGTGCCAGTTT | 1161 |
rs558369377 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905119 | GAAATTAAGAAAATA[C/T]AAGCCTGTGGCTCAC | 1161 |
rs558399731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927649 | AAGTGGCTGGCTGGA[A/G]TAACAGTATTGATTA | 1161 |
rs558439577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905868 | AAGGTAGTTTGGGGG[A/G]AGGGGTGGGAGTGGT | 1161 |
rs558544304 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882672 | GATTACAGGCGTGAG[C/G]CACCACTCCTGGGCA | 1161 |
rs558557208 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886573 | CAGGCGTGGTGGCGG[G/T]TACCTGTAATCCCAA | 1161 |
rs558673403 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883677 | ACACAAGTGATATGT[A/G]AAACAGTTATGTATT | 1161 |
rs558737345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918922 | CACCATCCATAAAAA[C/T]ATAACATGTTGAAGA | 1161 |
rs558904437 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60874856 | AACCCATATACAATA[A/T]AAGATAATGTAACTT | 1161 |
rs558964045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926443 | GCATGTATTGATTTA[C/T]AGACTTGTTTTTAAG | 1161 |
rs558977466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908319 | GAACTTCTGGATTAG[A/G]GACACTCAGTACATA | 1161 |
rs558984501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934469 | CTTGAATATTCTGGA[A/T]ATTAGTCCTCTGTTG | 1161 |
rs559005098 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946425 | TATCACTCAATTAAT[G/T]TATTTTTGCCTGGCC | 1161 |
rs559007904 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923401 | TTAAATGGGATTTTT[A/C]AATATGATCTTATTA | 1161 |
rs559019732 | in-del | -/CC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897120 | CTCAGGGTCTTTGTA[-/CC]TTTTTTCTTTCCCTG | 1161 |
rs559026655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919351 | TACAACTCTCCAATC[C/T]TGTATATGTTTGAAA | 1161 |
rs559038234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900066 | AAGTTCCTTACCATA[A/C]CTTTTCTACTGCTTG | 1161 |
rs559078883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914977 | TGTATGTTGCTAGAT[C/T]CTACATATTAATAGT | 1161 |
rs559102952 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878386 | TGATGCTGACCTCAT[A/C]AAATGAGTTAGGGAG | 1161 |
rs559175991 | snp | C/T | | | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874204 | TGATATAATCATTCT[C/T]GGCAAAATCATTCTT | 1161 |
rs559222555 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880271 | CGTTTGTGGGTAACC[C/T]GACCTTTCTCTCTGG | 1161 |
rs559308452 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930639 | GCTGAGGCAGGAGAA[A/T]CGCTTGAACCCAGGA | 1161 |
rs559324473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933679 | GTACCCATCACCCAA[A/G]CAGTACATACTGTAC | 1161 |
rs559420558 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932947 | GCCCTGGTGTCTTTT[-/A]AAAATCACCTTTCCA | 1161 |
rs559437802 | snp | C/G | | | missense | ERCC8 | GRCh38.p7 | 5:60887501 | AGAATGTTGCAGTCT[C/G]TGCTACCACTATAAA | 1161 |
rs559504555 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941217 | TGTTAAAACAGAAAG[A/T]CTCAGCAAAGAAATA | 1161 |
rs559527786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899404 | AAATTTCTACTTTTG[A/C]AAATTTGGGGGCAAA | 1161 |
rs559529644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914656 | TTAGCCGGAGATGGT[G/T]GTGCACACCTGTAGC | 1161 |
rs559540755 | in-del | -/GTGGT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906377 | CCTCCTCCTAGTCTG[-/GTGGT]CTCTCATTAGCTTTA | 1161 |
rs559562775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921397 | TCATTATCAGATTGA[A/G]TGTAGGTGAAGAGAA | 1161 |
rs559593730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892772 | AGCATCCAGCAGCCG[A/G]ATGAACTTGTCCAGG | 1161 |
rs559628942 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914547 | TGTAATCCCAACACT[A/T]TCAGAGGCCAAGGTG | 1161 |
rs559675941 | snp | C/G | 0.000399281 | 0.0141238 | missense | ERCC8 | GRCh38.p7 | 5:60898349 | GTGAGGAGGTGAAGT[C/G]CATCACTTGTAAAAC | 1161 |
rs559710537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941836 | AGGAATAAAGAGACA[A/G]CAACAGAAATAACTA | 1161 |
rs559815718 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60887039 | TTGAATGTCCAACCA[C/T]GATATGAACTATGTT | 1161 |
rs559824753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881600 | GCCGCCTTGCAGTTT[A/G]ATCTCAGACTGCTGT | 1161 |
rs559827832 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926327 | TTGTTACAAACATGT[C/T]TTAGCTCCTTTAAAT | 1161 |
rs559846343 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945587 | CTGGGCGCCTTGGCC[A/C]GGCCTCGTGCGTCCG | 1161 |
rs560001469 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892176 | CTACATTGAGTTTAG[C/G]CCACCCCATCTGATG | 1161 |
rs560008807 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900880 | AAAAATGTAAAATCC[A/C]CCCAAGCATAACCAG | 1161 |
rs560015570 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912326 | CCTTGTAAGTTGGAC[A/T]TCTAGGTATTTCATT | 1161 |
rs560038641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913628 | GTTATTTCTTGGCTT[C/T]TGCTAACTTTTGAAT | 1161 |
rs560115248 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931012 | TACTCAGGAGGCTGA[C/G]GTGAGAAAATTGCTT | 1161 |
rs560198313 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889176 | CTAACTTAGATTATT[C/G]GATGAAGGTGATATG | 1161 |
rs560349603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876833 | CATTCTGTAGGTTGC[C/T]TGTTCACTCTGATGG | 1161 |
rs560380620 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909433 | TCCATAGTTATACCA[A/C]GTGTGGCTGCCTCTC | 1161 |
rs560409554 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916623 | TGTATTTTAAATAAA[A/T]ATACTTTATTATAAA | 1161 |
rs560441911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902182 | ATTAGCACTGTGTTA[C/T]ACATTTGTGTGTAAG | 1161 |
rs560508008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876131 | AGAACTTGGCGGTGT[C/T]TGGGTTTTTGTCCTT | 1161 |
rs560508772 | in-del | -/AT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908564 | CATTCATATAAATAC[-/AT]ATATATATATATATA | 1161 |
rs560543122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927715 | ATCTCCTGCTGCTCA[C/T]GTCTGCATGTTTCAT | 1161 |
rs560563099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893909 | CTCTAGAACTCTTCA[A/T]CTTGCAAAATTTTAC | 1161 |
rs560567534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876501 | AGTCCCACCAACAGT[A/G]TAAAACTGTTCCTAT | 1161 |
rs560639211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934913 | TCTCCACTCTGTTCC[A/G]TTGGTCTATATGCCT | 1161 |
rs560693030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883769 | CTGCCCTATAGATCT[C/T]AGGCAGGAAAAAGTA | 1161 |
rs560813545 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886658 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 1161 |
rs560825715 | snp | A/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946766 | TAATAGAATAATTCC[A/G]TCACCATCAGAATTT | 1161 |
rs560842838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894312 | AAGGAAATAATTAAA[C/T]AGCAAAAGCTATATG | 1161 |
rs560877872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938456 | TCTCCAGAGTTCAAG[C/T]GATTCTCCTGCCTCA | 1161 |
rs560886111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927182 | TTTTGTAAAATAACA[C/T]CTTACTTTGAAAATC | 1161 |
rs560901171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879328 | TGTGGTGTGGTGCTG[A/C]AAAGAATGTATACTC | 1161 |
rs560998663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941641 | CATAATTAAACTGCT[A/G]AAAACTAAAGACGAA | 1161 |
rs561001438 | snp | A/G | 0.00018128 | 0.00951879 | synonymous-codon, intron-variant | ERCC8 | GRCh38.p7 | 5:60904801 | ACAAACCTGCTACCA[A/G]ACAGTGCTTGGTGGA | 1161 |
rs561059355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913843 | TTCTGCCTTCATTTC[A/G]TTATGTACCCAGTAG | 1161 |
rs561122971 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888179 | TTTATTTTTATTATT[A/G]TACATCTCAAAAACA | 1161 |
rs561208684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934788 | CCTCCATGTGGCTTG[C/T]CAATTGTCCCAGGAC | 1161 |
rs561241962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878220 | ATCCCAGGGATGAAG[C/G]CCACTTGTTCATGGT | 1161 |
rs561243640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883245 | ATATGAATGCATTAC[A/C]GTATTTTAGAAATAC | 1161 |
rs561326700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912138 | GTGAAGAAAGTCATT[C/G]GTAGCTTAATGGGGA | 1161 |
rs561353893 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934175 | CACTGTTTTCCATAG[C/T]GGTGGTACTAGTTGA | 1161 |
rs561366032 | snp | C/T | | | missense, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918282 | GTAATGTATTTGTAT[C/T]CCATACTTTCAGAGT | 1161 |
rs561449161 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916871 | GTTACTGTACATAGC[A/G]CTGAATTTAGTAATG | 1161 |
rs561465264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933848 | TTCCATTCCTGAGTT[C/T]CTTCACTTACAATAT | 1161 |
rs561481771 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60947031 | GTTCACAAGCTGAAG[C/G]ACATTAGGATGTTTC | 1161 |
rs561505002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881817 | GCTTCCCAGGTGAGG[C/T]GATGCCTCACCCTGC | 1161 |
rs561526122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926071 | CTCAGGTAATCCGCC[C/T]GCCTCGGCCTCCCAA | 1161 |
rs561580578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875518 | CTCATGCAAATAACT[A/G]AAAGGGCTTTAAGAT | 1161 |
rs561599360 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878164 | TTCTGTTTATATGCT[C/T]GATTACGTTTATTGA | 1161 |
rs561623972 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904549 | TATTCTCTGAATCCT[G/T]GCCACAGCATAGTGC | 1161 |
rs561653447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918989 | GGTGGTATGCTGTCC[G/T]GAAGGATGCAGTATA | 1161 |
rs561702668 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880317 | TTTCCTTCATTTCAG[C/T]TTTAGTGAATCTGAC | 1161 |
rs561769293 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909233 | AATGCAGACAAAAAT[A/G]CCCTATTCTGAAAAA | 1161 |
rs561820700 | snp | G/T | 1.65389e-05 | 0.00287562 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945036 | CACCGGCTGGAGCAC[G/T]GGACGTCGCCATGAC | 1161 |
rs561863457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930260 | CATGGCTAAACCCTG[C/T]CTCTACTAAAAATAC | 1161 |
rs561881848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944330 | TTGGCTCCCACTCTT[C/G]TTCTCAGTTGCAACC | 1161 |
rs561924860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922940 | TTCCCTGATTGCAAT[A/C]TTTAAGCTGGTATGT | 1161 |
rs561998652 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874910 | CTTTATCCAAACACC[-/CT]GTTTCCTTTAATCAC | 1161 |
rs562126460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914314 | GATAGGTAGCTCTTC[C/T]TGTTGTGATCCCTTT | 1161 |
rs562143385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884487 | TCTCAAAAAAAAAAA[A/T]AAAAAAAGACTATGT | 1161 |
rs562220187 | snp | A/G/T | 5.19821e-05 | 0.00509792 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874599 | AGCAGAGACAAAAAG[A/G/T]TACTAAAGATGATAT | 1161 |
rs562439255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889336 | CCAGCCTAGATTCAT[G/T]AATTTATATTCTGTT | 1161 |
rs562439309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896826 | GGAATAGAACCACAT[G/T]AACAATTTATATATA | 1161 |
rs562486714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939522 | TTGCTTTTTGAGACA[A/G]AGTCTCGCTCTGTCA | 1161 |
rs562538393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60924369 | TTCCTAAGGAATGGC[C/T]AATGAGAACAACAGT | 1161 |
rs562573916 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934101 | ACTAGGTGGATACCC[A/G]GGAGTGGGAATGCTG | 1161 |
rs562595947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895597 | ACAAAGGTATTCAGT[A/T]AGTTCCTAGATTAAT | 1161 |
rs562596467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882301 | CAGCTAGAAGAGCTG[A/G]AAAACAATATATTAA | 1161 |
rs562684156 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911275 | TGTGTCCTGACTTTT[A/C/T]AATAATCGCCATCCT | 1161 |
rs562778817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896139 | TACAGGCATGCGCCA[A/C]CATGCCCGGCTAATT | 1161 |
rs562825383 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876586 | TCTAACTGGTGTGAG[A/G]TGGTATCTCATTGTG | 1161 |
rs562837177 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888071 | TGTCTACAGATATGC[C/T]GTTTGCTTATGGCTG | 1161 |
rs562856905 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881527 | TTTGATCTTCCCAGC[A/C/T]GCTTTGTTTACCTAC | 1161 |
rs562865648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910555 | CTTAATTTCTCTCAA[A/T]AATGTTCTAAAGTTC | 1161 |
rs562875013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923816 | ATCCCAATCAAAAAT[A/G]GGGGAACCATCAAAA | 1161 |
rs562888420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876861 | TGGTAGTTTCTTTTG[C/T]TGTGCAGAAGCTCTT | 1161 |
rs562941564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921248 | ATAGCAAATCTCCTC[C/T]GAAATATTCCATAGC | 1161 |
rs563004879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914410 | GACCAGGATTGCAAC[C/T]CCTGCTTTTTTTTTG | 1161 |
rs563034364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881217 | AGCTGATCGTTCCTC[G/T]GGGAGTTTTGTCTCA | 1161 |
rs563067147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914904 | TGATGAATTACATTA[G/T]TTGATTTATAGATGT | 1161 |
rs563092199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879813 | ATGGGTCTTGACTCT[G/T]TATCCAATTTGCCAG | 1161 |
rs563169273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938771 | GTATCTACTAAATCT[A/G]GTTTGTTGTTTCTTC | 1161 |
rs563230640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931929 | CCCTGTATGTAACCA[A/G]TCTCCCATCTCCACT | 1161 |
rs563233283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884392 | GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAGGC | 1161 |
rs563271859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920615 | AAATTGGATTGTAAA[A/T]CCTTCAGATGTATAA | 1161 |
rs563468277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928596 | TCTAGCACCTAAAAG[C/T]CCTCTGCATCCAAAA | 1161 |
rs563498771 | in-del | -/CCT | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911229 | TCTCCACATTCTCCC[-/CCT]ATTTCTCCACATACT | 1161 |
rs563503973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935394 | TTAATTTTGTATCCT[A/G]AAACTTCGCTGAATT | 1161 |
rs563566732 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893493 | GCACTTTGGAGGTTG[A/C]TTTCTTCCCATTTTG | 1161 |
rs563580519 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906154 | GGCTGGCAATCATTT[A/C]TGTCTCTTTATTTAT | 1161 |
rs563588117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879382 | TGTAGATGTCTATTA[A/G]GTCTGCTTGGTGCAG | 1161 |
rs563588787 | snp | A/C | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943755 | ACAATGACACTGCCG[A/C]CATTTGAGACATTCT | 1161 |
rs563687554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905330 | CATTTTCAGCTTTTC[C/G]CCCTCCAAATACTCT | 1161 |
rs563748987 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897921 | ACATTTCAGATTTCA[G/T]ATTTTCAGATTAGGG | 1161 |
rs563788458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887644 | ATTTCTACTCCCTAA[A/G]GAAACTAGGCCAATG | 1161 |
rs563850386 | snp | C/G | 1.64885e-05 | 0.00287123 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887527 | ATAAAGTTCCTATAA[C/G]ATAGAAGGCAAAGAT | 1161 |
rs563929429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919608 | TCTGTAAATATTCAT[A/G]TATTTTAACTAATTT | 1161 |
rs563931625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912244 | GAATGTTCTTCCATT[C/T]GTTTGTGTCCTCTTT | 1161 |
rs563964421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894548 | ATGTATTTGGGACAA[A/G]AATTAAAATTCTTTG | 1161 |
rs564034529 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885519 | CAATAATTACATAAA[G/T]AAATGTAAAATAAAT | 1161 |
rs564059721 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931452 | GCTAGGACTACAATT[C/G]CATGTTACCACACCT | 1161 |
rs564096627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944063 | AGTACAACTTGCTTC[C/T]TCCCTTTGGAAAACC | 1161 |
rs564105662 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876110 | TTCAATTCCCACCTA[C/T]GAGTGAGAACTTGGC | 1161 |
rs564145557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937859 | ATAGCAAAAGTTCAC[A/G]ATATGCATCTCCATA | 1161 |
rs564147987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938515 | TGTGCCACCACACCC[A/G]GCTAATTTTTGTATT | 1161 |
rs564156747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902594 | TGCCTGATTCTGAAG[A/C]AAGTGAGGCCAAATA | 1161 |
rs564210816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938876 | CCTTACCTAATATTC[A/G]TAGTGATGTCCACAT | 1161 |
rs564219176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895439 | GGTTTTAAACACTCA[A/T]CTTTTTTTTGCCCCT | 1161 |
rs564326628 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945495 | GACACTTAGGGTGTC[A/T]CCGGAGAGAATTTCC | 1161 |
rs564327228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916392 | GTGTGGAAAGTTGAA[C/T]GCATTTCTGTAAGTG | 1161 |
rs564391131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930332 | GGACTTTGGGAGGCC[A/G]AGGATCACAAGGTTA | 1161 |
rs564415105 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880827 | TTCCTCCTTTAGCCC[A/G]GAGTAGTTTGATCGT | 1161 |
rs564436998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885701 | TAAAGATTTATCAAA[A/G]GGTATTTTTTTCTCT | 1161 |
rs564446875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893768 | GGGGCGGGGCTTCTC[C/T]CTTCCCTTTATAGTT | 1161 |
rs564461216 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938412 | AGGCTGGAGTGCAGT[A/G]ACACTATGTCGGCTC | 1161 |
rs564481368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937535 | TCCCAGGGGGATTAT[A/G]GCTGCCTCTGCTGTG | 1161 |
rs564529346 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911554 | GTTGCATGTTCACTT[A/G]ATGGTAGTTTCTTTT | 1161 |
rs564529840 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880379 | GAGTATCTTTGTGGC[A/G]TTCTCTGTTTTTCTG | 1161 |
rs564564565 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880841 | CGGAGTAGTTTGATC[A/G]TCTGAAGCCCTTTTT | 1161 |
rs564715290 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904670 | TATATATATATATAT[A/G]TATATATATATATAA | 1161 |
rs564728381 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926207 | AAAGATTTTCATCTG[A/G]TTTTGAACAAAATAC | 1161 |
rs564764372 | snp | C/G/T | 0.0115187 | 0.075054 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878486 | GTAGAATTCGGCTGT[C/G/T]AATCCATCTGGTCCT | 1161 |
rs564781169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893435 | TTTATTTCAGCCTCT[C/T]GATTGGCATGATCAT | 1161 |
rs564879701 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946137 | CTGTCCATTGAAATC[A/G]CACTGTGTAGCCGCC | 1161 |
rs564910199 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883027 | TAGGTGGATAAGCCA[C/T]ATGAGGGCCATGCTT | 1161 |
rs564931829 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923961 | ATAGTTCATAGTTCA[C/T]CACCTTAGAGTGTAC | 1161 |
rs564977621 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946732 | GACAAATGAGTAGAG[C/T]AACCTCACTGGATTC | 1161 |
rs565052971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912045 | CCTCCAGCTTTGTTC[C/T]TTTGGCTTAGGATTG | 1161 |
rs565111737 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888100 | TGAACAATGCTCATG[C/G]CCCTCCCCAACAAAA | 1161 |
rs565162675 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881564 | CTCAGCAATGGCGGG[C/T]GCCCCTCCCCCAGCC | 1161 |
rs565227548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881811 | CCTTGTGCTTCCCAG[G/T]TGAGGCGATGCCTCA | 1161 |
rs565234348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877483 | CATGGCCATTTTCAC[A/G]ATATTGATTCTTCCT | 1161 |
rs565247324 | snp | C/T | 3.34756e-05 | 0.00409105 | intron-variant, missense | ERCC8 | GRCh38.p7 | 5:60903639 | CCGTTTGAAATAAAA[C/T]AAAAATACCCTGTAG | 1161 |
rs565275111 | snp | A/G | 1.65633e-05 | 0.00287774 | missense, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918329 | GATGTGAACATGCCA[A/G]TGTCATGAGGATACC | 1161 |
rs565377366 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936253 | AATCTAGGAGGGTTG[C/T]GTATTTCCAGGAATT | 1161 |
rs565470569 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894853 | AACAAAATCCACTGT[A/C/T]GTCAGGGCTAATATT | 1161 |
rs565510437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879498 | ATTATTATTGTGTGG[A/G]AGTCTAAGTCTCTTT | 1161 |
rs565541771 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913336 | GAGGGTGTGTGTGTC[A/C/G]AGGAATTTATCCATT | 1161 |
rs565580621 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876731 | TTGATGGGGTTGTTT[A/G]TTTTTTTCTTGTAAA | 1161 |
rs565664538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898990 | ATATGAAATATATTA[C/G]AATGAACTATATAAA | 1161 |
rs565721233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882802 | CATCCAAATGTTTAC[C/T]GAATTTCCTGTCTTT | 1161 |
rs565773632 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874211 | ATCATTCTTGGCAAA[A/G]TCATTCTTAAAGGTG | 1161 |
rs565802356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914054 | ATGTGGTGCTGGGAA[A/G]AATGTATATTCTGTT | 1161 |
rs565841440 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873607 | GCTTGAACCTGGGAG[A/G]TGAAGGTTGCAGTGA | 1161 |
rs565886211 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941284 | TTCAATATAAAATTA[A/T]TTTAACTTAATGTAT | 1161 |
rs565913220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891624 | AAGAATGGTATTTTT[G/T]GGGGAGGGGGTAATG | 1161 |
rs565979397 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938709 | GTAAATGTACCACTG[A/C]CTTACAAAAAGTATG | 1161 |
rs566125218 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910125 | ATACATAGATTTTCA[A/G]CTGTGATGGGGGTCA | 1161 |
rs566141918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927342 | TTCCACAGAATGTAC[A/G]CTTTCCTTTTAATAT | 1161 |
rs566175472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881287 | CTGGGGGGTGCCTCA[C/G]AGTTAGGCTACTCGG | 1161 |
rs566262927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881278 | CTGCCCCTACTGGGG[C/G]GTGCCTCACAGTTAG | 1161 |
rs566362889 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940515 | AGGGAGTCCCAGAGA[A/T]CTGGGAAGCATCCAG | 1161 |
rs566424107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934472 | GAATATTCTGGATAT[A/T]AGTCCTCTGTTGGAT | 1161 |
rs566445140 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887606 | TTTTGAAATAATTAG[A/G]TCATAATAATTAGAT | 1161 |
rs566477218 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945167 | GAGGCCGACCTGACT[G/T]CTCCGCCTCGGTGGG | 1161 |
rs566484307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931478 | CACCTGGCTAAGTTT[C/T]GGTATTTTTTTGCAG | 1161 |
rs566546906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923976 | TCACCTTAGAGTGTA[C/T]ACATGAATATTAGCT | 1161 |
rs566579801 | snp | A/G | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919150 | TTTTGTGTATTTAAG[A/G]TAGTGGTACTGTAGT | 1161 |
rs566580483 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925970 | CTGGGATTACGGGCA[C/T]GCGCCACTGCACCTG | 1161 |
rs566583898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941218 | GTTAAAACAGAAAGT[C/T]TCAGCAAAGAAATAG | 1161 |
rs566590120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906368 | GGCTTGTCTCCTCCT[C/T]CTAGTCTGGTGGTCT | 1161 |
rs566606258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894151 | CACCACGCCCGGCTA[A/G]TTTTTTGTATTTTTA | 1161 |
rs566606824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924714 | GTTCTATATATACAC[C/T]TCTTGAATTATTTTC | 1161 |
rs566718619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932571 | AGGAATAGAGTGTGT[C/T]CTGTGTGACTCCACT | 1161 |
rs566735064 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937583 | GAAGTTGGGGAAGGC[C/T]GGCAGCCAAAGGCTT | 1161 |
rs566778969 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892403 | GTATCCTCGATGTCA[A/G]AGAACTTGGTCATTT | 1161 |
rs566797017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929491 | ATGCAGGAGACTGAG[A/G]CAGGAGGATTGCTTG | 1161 |
rs566806285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938574 | GGCCACGCTGGTCTC[A/G]AACTCCTGACCTCAG | 1161 |
rs566820151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930874 | CACTTTGGGAGGCCA[A/G]GGAGGCCGGATCACT | 1161 |
rs566934708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884773 | AATTACTTTAGCACA[C/T]ACCATTTTATATTAA | 1161 |
rs566991221 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900539 | TATTTTTTATTTAAT[A/T]TTTTTAAAAAAATAT | 1161 |
rs567026432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884033 | TTGATTGATGGGGAG[G/T]TAACTCTCATCTGAA | 1161 |
rs567085979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922339 | TCTTAATATTTAATA[C/T]AAGAATGAATATAAA | 1161 |
rs567100530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60885859 | AAATTATATTTTCAT[A/G]TGGTTTTTGACATAG | 1161 |
rs567117293 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880009 | TGGCTGGTACCGGTT[G/T]TTCCTTTCCATGTTT | 1161 |
rs567119903 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912634 | CAACGCTATGTTAAA[C/T]AGGAGTGGTGAGAGA | 1161 |
rs567130895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925703 | GGGGTTTGTAGGGAT[A/G]CTTCATGACCTAGTT | 1161 |
rs567160110 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875177 | AATAAGGTATTCAAG[A/C]TGAATAATACCATTT | 1161 |
rs567179737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880484 | TGGTTCCATTCTCCC[C/T]GTCACTTTCAGGTAC | 1161 |
rs567197523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926342 | CTTAGCTCCTTTAAA[C/T]GGTGTGTGTAATGAT | 1161 |
rs567207499 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913107 | TGATGCTGGCCTCAT[A/C]AAATGAGTTAGGGAG | 1161 |
rs567326648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905027 | TACCCCAAAAAACCT[C/T]GATAATTTGAAATCC | 1161 |
rs567360488 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915188 | TAGAATAACTTACTC[A/G]TAAAGGCACCTAGGC | 1161 |
rs567367692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896341 | CCTGTGTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 1161 |
rs567392961 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882485 | CTGCAACCTCTGCCC[C/G]CCAGGTTCAAGTGAG | 1161 |
rs567417438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918675 | CAGCCAACTACACTG[A/G]TCTTCTTTCATCTTG | 1161 |
rs567465617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933530 | GCCCCTGTATTTTCT[A/G]TCTACTATATATTAC | 1161 |
rs567491516 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876984 | GAATGGTAATGCCTA[A/G]GTTTTCTTCTGGGGT | 1161 |
rs567498692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878082 | AGTTTTTAGCATGAA[A/G]GTTGTTGAATTTTGT | 1161 |
rs567542722 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939594 | CCACCAAGAGATCCT[C/T]GTGCCTCAGCCACGT | 1161 |
rs567572304 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939323 | TCATCTTTAATGTTC[C/T]TTCGGATTTCATTCA | 1161 |
rs567608321 | snp | A/C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894854 | ACAAAATCCACTGTC[A/C/G]TCAGGGCTAATATTG | 1161 |
rs567636973 | in-del | -/AGTCTCATTCTATT | 0.000798403 | 0.0199641 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918752 | GATTTGCTTTTCCAA[-/AGTCTCATTCTATT]AGCACTACTATTCTT | 1161 |
rs567640997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60903114 | TTTCTTAACATATTT[G/T]TTATGTGTTTCTTTG | 1161 |
rs567684336 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874502 | AAACATGAGGAAAAA[C/T]ATTACCCACATTTAG | 1161 |
rs567703088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893204 | AATCACATCAGAGTA[C/T]TCTACCACCTCACGG | 1161 |
rs567753229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909847 | TAGTCCCAGATACTC[A/G]GGAGGCTGAGGCAGG | 1161 |
rs567763544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893644 | ACTTCCGGCGGGGAT[C/G]TGAGAAGAGAGAGTA | 1161 |
rs567869945 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874849 | AAGAAACAACCCATA[C/T]ACAATATAAGATAAT | 1161 |
rs567905641 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945774 | ACCAAAGGGGCTAGA[A/C]GGGCCAGGGGAGGGG | 1161 |
rs567906188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910850 | TGTCCAGTTCCTATC[C/T]CTTTTATTTCCTTTG | 1161 |
rs567954129 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899336 | GGCATTGAATATGTA[C/T]AGTTGGCCTCAATGG | 1161 |
rs568016247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942978 | TGATGGAAATATTTT[A/T]AAAAAAATTTTAGGC | 1161 |
rs568046252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937647 | GCTGGTTTCACTCCC[A/C]CTGCGCCCCTACAAC | 1161 |
rs568082638 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943621 | ATTAAAAGAGGAAAT[A/T]GGCCAAAAGAATGAA | 1161 |
rs568109584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929698 | TAAGACAAATGACAT[A/T]TCTGATATTTTATAA | 1161 |
rs568192190 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938095 | TATATATTTTATTTT[A/T]TTTTTTTTTAGGTTA | 1161 |
rs568206790 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874338 | ATCTGCTGAAGGTCA[A/C]AACTGAGGTACAACG | 1161 |
rs568228920 | snp | A/C/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946652 | CAGACTGAGTTTTTT[A/C/T]AAATTGAAATATAAT | 1161 |
rs568230940 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891479 | TTTATTAATGCAACC[A/G]TTCTTTTCAAAAGAA | 1161 |
rs568278712 | in-del | -/AAAAATAAAAAT | 0.0508889 | 0.151178 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886704 | GAGACTCCATCTCAA[-/AAAAATAAAAAT]AAAAATAAAAATAAA | 1161 |
rs568357264 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885652 | TTAGACGTGATAAAA[A/T]CTGGAAGTATGCATA | 1161 |
rs568394210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879589 | TTAGGATAGTTAGCT[C/T]TTCTTGTTGAATTGA | 1161 |
rs568507219 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878855 | TTGAAGGGTTTTTTG[A/T]GTCTCTATTTCCTTC | 1161 |
rs568536220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920913 | TAAGATAAAAATGAA[G/T]TTAATTAATTAACAT | 1161 |
rs568536256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928775 | TTTCATTAATTTTAA[C/T]GAAACTTCTACATCA | 1161 |
rs568576568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914100 | GTTCTGTAGATGTCT[A/G]TTAGGTCTGCTTAGT | 1161 |
rs568593616 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945628 | TACCCAGCGCCTTCC[A/C]CCGGCGTGCCCCGGG | 1161 |
rs568638107 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904023 | CTAAGTTTCCCCAAC[A/G]ATTATGTGTGAGGTA | 1161 |
rs568643711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941953 | ATGTAAATATAAAAT[A/G]TAAGACAACAATATA | 1161 |
rs568654429 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898009 | AGTCCTCAGTCTTTT[A/C]TTTTTCTCTACTACG | 1161 |
rs568656878 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945233 | GTCCCGCTGCTGGCA[G/T]CGCTGGAAACTGGGT | 1161 |
rs568669740 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933289 | TGTGGTGCAATCTCG[A/G]CTCACTGCAACCTCC | 1161 |
rs568718483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934968 | TTTTGGTGACTATGG[A/C]CTTATAGTATAGTTT | 1161 |
rs568770773 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907188 | TCAAATCTTCTCCAC[A/T]AATATACCAACTCAG | 1161 |
rs568847513 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892128 | GTCCACTGGGCACAC[A/G]TCCACCTTACTGTTT | 1161 |
rs568851278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877748 | CTTTGCTGAAGTTGC[C/T]TATCAGCTTAAGGAG | 1161 |
rs568861141 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877110 | TATGGCTAGCCAGTT[A/T]TCCCAGCACCATTTA | 1161 |
rs568876645 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926067 | TGACCTCAGGTAATC[C/T]GCCCGCCTCGGCCTC | 1161 |
rs568906796 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916803 | TTTTATTACTTTTTA[C/G]TATGTGGCCAGTTAC | 1161 |
rs568910017 | in-del | -/TC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889275 | GAGATTATATAAATA[-/TC]TCATTCCTCATCAAA | 1161 |
rs568944077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925463 | CCTTCTGGTCTTACC[A/G]TGGGCCACTCAAACA | 1161 |
rs568974911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938605 | GTGATCCACCTGTCT[C/T]GGCCTCCCAAAGTGC | 1161 |
rs569038683 | snp | A/C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915898 | ATAGACATCTGGGAG[A/C/T]GGGACATGATGCTGC | 1161 |
rs569044081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895922 | GGCATTAACTTTTGT[C/T]TTGTCCTTAGGGTTT | 1161 |
rs569113668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939057 | CTTCTTAATGGAAGA[A/C]ATCAGCCTGTTCACC | 1161 |
rs569121057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887650 | ACTCCCTAAAGAAAC[A/T]AGGCCAATGCTGTTT | 1161 |
rs569125110 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923815 | TATCCCAATCAAAAA[C/T]AGGGGAACCATCAAA | 1161 |
rs569174430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932365 | AAGAATGGCTCACTG[C/T]GCCTAAACTATTTGA | 1161 |
rs569179699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923147 | AAATTAGCAGTATCT[G/T]TTTTTGGAAACAATT | 1161 |
rs569188371 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938564 | TCACCATGTTGGCCA[C/T]GCTGGTCTCGAACTC | 1161 |
rs569191733 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889463 | GGCATATACCACCAC[A/G]CCTGGCTGATTTTTT | 1161 |
rs569213989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60901449 | TAATCAGCTCCCTCA[A/C]TCTTTCAATCTATTA | 1161 |
rs569245858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60916079 | AAATTGCTGTTCTTC[A/C]AATGTCTTCTGCTTC | 1161 |
rs569296144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909626 | TGATTTTCTTAATAA[C/T]ATTTTCTTTTCTCTA | 1161 |
rs569299682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914016 | TTACTTCCAACTATG[A/T]GGTCAATTCTGGAAT | 1161 |
rs569357357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902242 | AAGGTGAAACACCTT[G/T]AAGGTGGATAGGATT | 1161 |
rs569400211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886851 | TATTAACAATTTTTG[A/G]ACAGATATTTACCTT | 1161 |
rs569422139 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941719 | AATGATTTGAATGGC[G/T]GCAGATTCCTTTTCA | 1161 |
rs569422317 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910722 | TAATTTACCTTGTAT[C/T]CAGCAAATTTGCTAA | 1161 |
rs569463377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880940 | AGGAGGAGAGGTGCT[C/G]TGACTTTTAGAGTTT | 1161 |
rs569477090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883374 | GAGACCCACTGATCA[A/G]GTGTCACTACTATTA | 1161 |
rs569503702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875771 | GCGCGATCTCCGCTC[A/G]CTGCAAGCTCCGCCT | 1161 |
rs569518863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919314 | GGTTGGTGAAGCTGG[A/G]TGATTGATACACAGG | 1161 |
rs569565109 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876179 | ATGATGGTTTCCAGC[G/T]TCATCCATGTCCCTG | 1161 |
rs569581839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919893 | GAAGAAAGGTGTATA[C/T]GCATGCTGGACAGCC | 1161 |
rs569622847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905760 | AGTAAAGAGTTTAAC[C/T]GATGCAAGGCTGGCC | 1161 |
rs569675327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898796 | TAGTGTTTTCCATTG[A/G]AAAAAAAAACAGGGA | 1161 |
rs569702100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889670 | GTAGAAAGAAATAAT[C/T]TGTGGTTAGAGTACC | 1161 |
rs569702232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897152 | ACTAGAATGATATCC[A/C]CCAGCAAACAACTGA | 1161 |
rs569754299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927313 | AAGTTATATACACAT[C/T]GATTTTTTTAGTTTT | 1161 |
rs569779159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878984 | CATTTTAGATCTTTC[C/T]TGCTTTCTCTTGTGG | 1161 |
rs569798075 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878535 | AAGCTATCAATGATT[G/T]CCTCAATTTCAGAGC | 1161 |
rs570019144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939790 | CTGCAATACTTCTTT[A/C]TTGTTAGTAGGTATC | 1161 |
rs570038044 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877626 | CTAGGTATTTTAATC[-/T]CTTTGAAGCAATTGT | 1161 |
rs570082261 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940512 | AACAGGGAGTCCCAG[A/T]GAACTGGGAAGCATC | 1161 |
rs570094399 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934872 | GAAGATCAGCTAGCT[C/G]TAAGTATTTGGCTCT | 1161 |
rs570099235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886182 | GGGAGAGAAACCACC[C/T]TTAAACAGCCTCTAT | 1161 |
rs570116466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934442 | TGTTTATCTTTTTCT[C/T]GATTTGAGTTCCTTG | 1161 |
rs570136549 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882662 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 1161 |
rs570137267 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883712 | GAATGTCAAAACAAA[A/G]TAAGATTCTTAGTGA | 1161 |
rs570172884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926371 | ATGTAGTAGATTTAT[C/G]TTTTAGCACAAGATC | 1161 |
rs570228059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911511 | TTGTCAGATGGGTAG[A/G]TTGCAAAAATTTTCT | 1161 |
rs570291077 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903837 | AAATATGAAGATATA[C/T]GCCAAAATTACATTG | 1161 |
rs570363114 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925893 | CAGTGGCATGATCTC[A/G]GCTCACTGCAACCTC | 1161 |
rs570401917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894129 | AGCTGGGACTACAGG[C/T]GACCGCCACCACGCC | 1161 |
rs570477480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938142 | ATAAGTTTCTCTGGG[C/T]CCCCTAAGTTGTAGA | 1161 |
rs570492164 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923305 | ATTGAACTTAATAAT[C/T]TGTAAAATCATTCTT | 1161 |
rs570566196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931303 | AACTTTAACATTAAA[A/T]TTTTTTTTAAATTTA | 1161 |
rs570719151 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879991 | TTTGGCATGTTTTTG[C/T]AGTGGCTGGTACCGG | 1161 |
rs570727617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60942716 | GTTCTCTTGATTATG[A/G]TAATGGTTTCAAAAG | 1161 |
rs570727728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935927 | TTTTTATATGCTGCT[A/G]GATTTGGTTAGCAAG | 1161 |
rs570762468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921684 | TATCAGGTGAAAATC[C/T]AATTTGTGTTTATAA | 1161 |
rs570808226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944444 | CTCATCTAGTTTCTG[C/T]CTACTTCATCTCTTG | 1161 |
rs570878497 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878688 | TATTCTGATGGTAGT[C/T]TGTATTTCTGTGGGA | 1161 |
rs570983498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60907556 | TGAGGTTTCACCATA[C/T]TGGCCAGGCTGGTCT | 1161 |
rs571060560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939168 | TAGTTTAATGAAGTT[A/G]CTATTCATTTCCATC | 1161 |
rs571063537 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932219 | AGAGGTGGGGAGTGG[C/T]AGGAGACAAGGTGTA | 1161 |
rs571106970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892933 | TGCGCATTTCACCAA[A/G]GCAGCAATAGTTCCC | 1161 |
rs571125640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879659 | TTTGTTGGTTTAAAG[A/T]CTGTTTTATCAGAGA | 1161 |
rs571197310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877919 | CTATGTTGAATAGGA[A/G]TGGTGAGAGAGGGCA | 1161 |
rs571203558 | snp | C/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918569 | ATCTCTAGATTCAGG[C/T]TCCCACTGTGTGATG | 1161 |
rs571217440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919219 | ATTATGAATAAACGA[C/T]AGGTTGTTCGAGATT | 1161 |
rs571296434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910644 | TGATTTTTGATGCTA[C/T]GGTAAACAATGTTGG | 1161 |
rs571396648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903986 | TTGCAAAGCTAGTAT[A/G]AAGAGAACCGTGTAC | 1161 |
rs571396727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912387 | TCATGATTTGGGTCT[C/T]TGTTTGTCTGTTATT | 1161 |
rs571429651 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925009 | AGATACTTCTTTCCG[C/G]TGTGACTTCACTATC | 1161 |
rs571513889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60916115 | TTAAGTCTATGGTCT[C/T]GCATAGCTTGGTCAG | 1161 |
rs571514757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881663 | ACCCTCCGAGCCAGG[C/T]GCAGGATATAATCTC | 1161 |
rs571540096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902336 | TCATTTTAAAGGAGT[C/G]AATTAATAATTAAAT | 1161 |
rs571555555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925574 | GTTGGTTACTTTGGA[A/C]TTATCCAGGTATATC | 1161 |
rs571576606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916919 | TCTTTGGGGAAGTAA[C/G]AATCTAGAACAACAA | 1161 |
rs571577030 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881988 | GAGCTGTTCCTATTC[A/G]GCCATCTTGGCTCCA | 1161 |
rs571591044 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60897951 | GATACTCAACCTATA[A/T]AAAATTTGATTACTT | 1161 |
rs571632827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909775 | CCTGGCCAACATGGC[A/G]AAACCCTGTCTCTAC | 1161 |
rs571665094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902848 | ATAAGATAAACATTT[C/T]AAAGGATAAAAATGT | 1161 |
rs571705379 | snp | C/T | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60920042 | GAAAGCAAGGGACTC[C/T]AGACATTCTCTTTTC | 1161 |
rs571712563 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60928457 | GCCAGGAAGAACTCA[A/G]ATATAATTCTTATTT | 1161 |
rs571729609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895824 | GGACACCTAGTTATA[A/C]AACTTATGGTCTTTC | 1161 |
rs571731423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60935132 | GTTTTTGGCAGTATG[A/G]TTATTTTCGCAATAT | 1161 |
rs571837512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876668 | TGTCTTTTGGCTGCA[C/T]AAATGTCTTCTTTTG | 1161 |
rs571859037 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928212 | TTGAGTTTTTCAAAG[A/C]ATTTTGGCTGCTGTG | 1161 |
rs571907473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941574 | TACAAGTTCAAGAAG[C/G]AGAATGAACCCTAAC | 1161 |
rs571915747 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934110 | ATACCCGGGAGTGGG[A/G]ATGCTGGATCAAATG | 1161 |
rs572039790 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931232 | CTGATTATAAGATTA[A/G]TAGAAGAGTAATTTG | 1161 |
rs572091987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878171 | TATATGCTCGATTAC[A/G]TTTATTGATTTGTGT | 1161 |
rs572152878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878588 | TTCAACTTCTTCCTC[A/G]TTTAGTCTTGGGAGG | 1161 |
rs572179339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912072 | ATTGTCTTGGTAATG[C/T]GGGCTCTTTTTTGGT | 1161 |
rs572190289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879252 | TTTGCTATAATTTCT[A/G]TTCTTTTACATTTGC | 1161 |
rs572192004 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884256 | AGGCCGAGGCGGGTG[A/G]ATCATGAGGTCAGGA | 1161 |
rs572239845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60912717 | CATTCAGTATGATAT[C/T]GGCTGTGGGTTTGTC | 1161 |
rs572302083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940834 | TATCAACATTCTTCA[A/T]AGGATCAAAACAAGA | 1161 |
rs572360175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926491 | TTATAAAACAATAGG[G/T]TTAATTTAAAAGTAG | 1161 |
rs572414159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918927 | TCCATAAAAACATAA[C/T]ATGTTGAAGACTCTA | 1161 |
rs572421165 | snp | C/G | 0.00159712 | 0.0282137 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919353 | CAACTCTCCAATCTT[C/G]TATATGTTTGAAATT | 1161 |
rs572424953 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882133 | GGCGTGAGCCACTGC[A/G/T]CCCGGCTTAGAAACA | 1161 |
rs572485164 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946492 | CCCTAATGAGCTCCT[C/T]TGTCAGGCAGGGAAT | 1161 |
rs572549879 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876346 | AATAAACATACGTGT[C/G]CATGTGTCTTTATAG | 1161 |
rs572591979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889053 | ATACAGCAGTTACTT[C/T]GTAGACTGCCCTTCA | 1161 |
rs572604285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889811 | GTTAGGGGCAAGTCA[C/T]GTCACCTCTCTGGTG | 1161 |
rs572631878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939464 | TTTGTTTGGATTCCC[C/T]GGTTGCAATACTTCT | 1161 |
rs572702407 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ERCC8 | GRCh38.p7 | 5:60932845 | AGGAGAGAGGAAAGA[G/T]TAGACACATAAAGGA | 1161 |
rs572744422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880289 | CCTTTCTCTCTGGCT[G/T]CCCTTAACATTTTTT | 1161 |
rs572807166 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901083 | AATCCAGACACAGAT[A/C]TTTATAAAATTAATA | 1161 |
rs572841074 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888886 | ATCTAAAGACCACAT[A/T]CATGTTTCATTATTT | 1161 |
rs572869722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60916292 | AAAGTCCCACTCATT[C/T]ATCTGCCTCTTAGAA | 1161 |
rs572924994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909164 | GCAGATGAGTTTCCA[A/G]ATACCATTAAGAAAA | 1161 |
rs572953350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944008 | TGTTCTCCAAGTAAA[C/T]ATCTTCACAGGTTCC | 1161 |
rs572960271 | in-del | -/CA | 0.0126979 | 0.078662 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890518 | GAAGAATAGATCATC[-/CA]CACATACATAAACCA | 1161 |
rs573033090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937314 | AGTATAGAAAGGATA[C/T]ATGCTTGCCCTAGGG | 1161 |
rs573041720 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889714 | CGGCTGTGTCTCTAA[A/G]TAACTTTGCAAAGAA | 1161 |
rs573094531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929241 | CATCTAATGGACAAA[A/G]GCATAAATTACAGGA | 1161 |
rs573120302 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923388 | TTACTGTGTTTTTTT[-/A]AATGGGATTTTTCAA | 1161 |
rs573160970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930158 | AAGCAGGCCAGGCGC[A/G]GTGGCTCATGCCTGT | 1161 |
rs573253809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60943067 | CTTCAGCCCAGGAGT[C/T]CAAGACCAGAATGGG | 1161 |
rs573270295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881818 | CTTCCCAGGTGAGGC[A/G]ATGCCTCACCCTGCT | 1161 |
rs573331777 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60880209 | CCCACTCTCTTCTGG[C/T]TTGTAGAGTTTCTGC | 1161 |
rs573354897 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923786 | TACATTTATCCCAAT[C/T]ACAAATATACATTTA | 1161 |
rs573388134 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920505 | GGAATCTTTTTAGTG[C/T]TCAAGGACAAACACA | 1161 |
rs573487213 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894811 | AAACCAGTAACTAAT[C/T]ATTTGGGAATCATGA | 1161 |
rs573514277 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914838 | TATTTCAAAATGTTC[A/G]TATCTATTGAGATGA | 1161 |
rs573567431 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946591 | GCAAGCAGAGAGATG[C/T]TTCTTTTCCATAAGT | 1161 |
rs573589511 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908585 | TATATATATATATAT[A/T]TTTTTTTTAAATAAT | 1161 |
rs573674255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60940099 | CCTCCTAATCTCTTA[C/T]CATTTTCATTACTGG | 1161 |
rs573674598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904195 | CTAGTAACAGATTCA[A/C]AGAAACTGGACACAG | 1161 |
rs573676880 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896089 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 1161 |
rs573702199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60889967 | CTGCGTTAAGGTGAC[A/G]TCTAAGAGGTCCCAG | 1161 |
rs573706329 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902295 | TTTCTTTTGGTGACA[C/T]GAATTAAAATTTCTA | 1161 |
rs573718723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931883 | CCAGTAAGAAGCATG[G/T]CTCCCATTACTACCA | 1161 |
rs573786611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918157 | ACCACTGTACTGCTT[C/T]CACATCTAACATATA | 1161 |
rs573796597 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934850 | TTAGGTTTTTGTTTG[C/G/T]TTTGCTGAAGATCAG | 1161 |
rs573849152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877280 | CTGTTTTGGTTACTG[C/T]AGCCTTGTAGTATAG | 1161 |
rs573854630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911161 | GGTTTGCTGCACCCA[G/T]TAACTCATCATTTAC | 1161 |
rs573888439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911707 | TAGGTTTTCTTCTGG[C/G]GTTTTTATGGTTTTA | 1161 |
rs573984654 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943161 | CTGTGGTCCCAGCTA[A/C]TTAGGAGGATGAGAT | 1161 |
rs574013950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60895039 | AGCCAGGCCTGGTGG[C/T]GGGTACCTGTAATCC | 1161 |
rs574021616 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881476 | AAGTCTACAGAGGCC[A/G]GCAGGCCTCCTTGAG | 1161 |
rs574055648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881707 | TGCTAAGACCATTGG[A/T]AAAGTGCAGTATTAG | 1161 |
rs574087148 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60916270 | CTCTAGCTTTATGAA[A/G]TTGACTAAAGTCCCA | 1161 |
rs574094858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917471 | TGACATGATGAAACT[A/G]CTTTATAATAAGATT | 1161 |
rs574110741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928376 | AACAAGCTTGTTAGG[C/T]AGGTACTATTGTTCC | 1161 |
rs574173056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921233 | CAGAGCCAACAAACA[A/G]TAGCAAATCTCCTCC | 1161 |
rs574189147 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884912 | TGTGATTTTCTAACT[C/T]GTTTTGCTTAATTTC | 1161 |
rs574209678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894321 | ATTAAATAGCAAAAG[C/G]TATATGCCCAGAGGA | 1161 |
rs574238840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60921912 | TATTTTCAAGAAAGT[A/G]TCAAGGAACAGCCAT | 1161 |
rs574246018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938498 | AGCTGGGATTACAGG[C/T]GTGTGCCACCACACC | 1161 |
rs574268856 | snp | A/G/T | 3.29588e-05 | 0.00405938 | missense, synonymous-codon | ERCC8 | GRCh38.p7 | 5:60887449 | ATTTACCTCATCATC[A/G/T]TCAGGAACTGGTTCA | 1161 |
rs574306397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936189 | TATTACCATTTCAAT[C/T]TCATTGCTTGTTGCT | 1161 |
rs574328828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60884362 | GCGCCTGTAGTCCCA[C/G]CTACTCGGGAGGCTG | 1161 |
rs574329218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927857 | AAGTAAGATGTTTCT[C/T]ATATACTAGTAGATG | 1161 |
rs574388600 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879780 | ACGTGAGATGGGTTT[C/T]CTGAATACAGCACAC | 1161 |
rs574414457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892663 | ACTGCAAGATGGTCT[C/T]CACTGGGGTCATGGG | 1161 |
rs574441094 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930943 | GAAACCCCGTCTCTA[A/C]TAAAAATACAAAAAA | 1161 |
rs574456622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929072 | AATGTCTAAATCTTC[C/T]ACCACACATCCTAAC | 1161 |
rs574458035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60879159 | AGGAGGTTGTTCAGT[G/T]TCCATGTAGTTGAGC | 1161 |
rs574479478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880122 | TTTCTCCTTCACTTA[C/T]GAAGCTTAGTTTGGC | 1161 |
rs574573638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906654 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 1161 |
rs574585335 | snp | C/T | 3.36287e-05 | 0.00410039 | missense | ERCC8 | GRCh38.p7 | 5:60874629 | TTCATCCTTCTTCAT[C/T]ACTGCTGCTCCAGGC | 1161 |
rs574733425 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878230 | TGAAGCCCACTTGTT[A/C]ATGGTGGATAAGCTT | 1161 |
rs574743594 | in-del | -/CTCT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877666 | TCACTCGTGATTTGG[-/CTCT]CTGTTTGTCTGTTAT | 1161 |
rs574778375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60939941 | GTATACATACTTTTA[C/T]GTCTTTTTTATCAAT | 1161 |
rs574811292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913413 | CTCTGATGGTAGTTT[A/G]TATTTCTGTGGGATT | 1161 |
rs574873718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906094 | TTGTGATGTTATATG[A/C]AGGAGTAATTGGGGA | 1161 |
rs574893821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920112 | AGTCTGCGTTGGTGA[A/C]ATATAGCAAAACCCA | 1161 |
rs574918751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890716 | ATTGATTCATTCATA[C/T]ATTGTATGCTGTCTA | 1161 |
rs574933824 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60933942 | GTATTCCATGATACA[C/T]ACACACACACACACA | 1161 |
rs574975913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882911 | TGACTCCTCTTCCCT[A/G]CTCTGTCTCTAGAAG | 1161 |
rs575052712 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875697 | TTTATAACTTAGAGA[A/C]ATTTTTTTTTTCCTT | 1161 |
rs575170322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926597 | AAAAATATTCCACAT[C/T]AGCTTTATTACATTT | 1161 |
rs575199012 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894040 | CCCAGGCTGGAGTGC[A/C]GTGGCGCGATCTAGG | 1161 |
rs575200947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943199 | TCATTTGAGCCTGGA[A/G]AGTCGAGGCTGCAGT | 1161 |
rs575265131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944038 | CTCAATTAATGTGGG[A/C]AAAATTAAAAGTACA | 1161 |
rs575312179 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884447 | TGCCACTGCACTCCA[C/G]CCTGGGTGACAGAGC | 1161 |
rs575350927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938386 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCAGGCT | 1161 |
rs575414199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60930890 | GGAGGCCGGATCACT[C/T]GAGGTCAGCGATTCA | 1161 |
rs575436431 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881025 | CTTTGATGATGGTGA[C/T]GTACAGATGGGGTTT | 1161 |
rs575441034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944851 | AGGAGAGCGATGAGA[A/C]GGGAAAGTGTGGGGC | 1161 |
rs575462614 | in-del | -/CCAC | 0.00557542 | 0.0525036 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927843 | TAACCACATGCTAAA[-/CCAC]GTAAGATGTTTCTCA | 1161 |
rs575487960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887063 | CTATGTTAAAAAACA[C/T]ATGCATAGGAAAAAA | 1161 |
rs575492003 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885663 | AAAATCTGGAAGTAT[A/G]CATATGGCATTGGGT | 1161 |
rs575494804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876369 | CTTTATAGCAGCATG[A/T]TTTATAATCCTTTGG | 1161 |
rs575524917 | snp | C/T | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919783 | AACTTAGGATCATCA[C/T]CCTTTGGGGAAGAGG | 1161 |
rs575552890 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899151 | TATATTTCTGGTCCA[A/G]AATTAATTCTCTATC | 1161 |
rs575588021 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60923603 | GCAAATATTTCAGGT[C/T]ATTTTCACTGTTTTT | 1161 |
rs575593664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60900564 | AAATATACACACAAG[G/T]TTTACTGGTTTCTAT | 1161 |
rs575610147 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891818 | AGACACATAGTTGGG[G/T]AAGGGTTCTTTTAAT | 1161 |
rs575641246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937845 | CTGTGGTAGTTCTTA[C/T]AGCAAAAGTTCACGA | 1161 |
rs575651348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916322 | AGCTATCCAATGCCT[A/G]TCTTCTCAGTCTCTT | 1161 |
rs575652963 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924051 | GGTCTCCTCTACCTT[A/T]CTTCCTCCCTCCTGT | 1161 |
rs575660280 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937244 | AATGTACTGGTTTTG[C/T]GTTGGTTGGCCTCCA | 1161 |
rs575722143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60941397 | AGAGGAAAAAAGATC[G/T]AAGGGAAAAAGAACA | 1161 |
rs575814414 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930864 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGAGG | 1161 |
rs575820550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908005 | GCAATCTTTTACAGG[C/T]TTCCATTGTATCATA | 1161 |
rs575831812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894240 | CTGCCTGCCTTGATC[A/T]CCCAAAGTGCTGGGA | 1161 |
rs575833486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60911836 | TTTCCCAGCACCATT[G/T]ATTAAATAGGGAATC | 1161 |
rs575920981 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934604 | TTGTTTTTGTCGTGT[C/T]TGCTTTTCGGTTCTT | 1161 |
rs575928066 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60908587 | TATATATATATATTT[A/T]TTTTTTAAATAATGG | 1161 |
rs576078323 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60934613 | TCGTGTTTGCTTTTC[A/G]GTTCTTGGTCATGAA | 1161 |
rs576249082 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904666 | TATATATATATATAT[A/G]TATATATATATATAT | 1161 |
rs576278857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888072 | GTCTACAGATATGCT[A/G]TTTGCTTATGGCTGA | 1161 |
rs576287182 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60905084 | CTATGAAAAAAAATA[C/T]GTTTTCCCAATAAAT | 1161 |
rs576312633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60896828 | AATAGAACCACATGA[A/G]CAATTTATATATACA | 1161 |
rs576353661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60888988 | TTTAGTTTTCAAGCT[C/G]GAACAGTTCTTCAGT | 1161 |
rs576396953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882079 | ATCTCCTGATCTCGT[C/G]ATCTGCCTACCTCAG | 1161 |
rs576401713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925260 | AAGCTTACTTTCAGA[A/G]ATTTCCTGTTTCTGT | 1161 |
rs576408264 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904188 | CCAATCACTAGTAAC[A/G]GATTCACAGAAACTG | 1161 |
rs576421742 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ERCC8 | GRCh38.p7 | 5:60877444 | GATGGGGATGGCATT[C/G]AATCTATAAATTACC | 1161 |
rs576441452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60925865 | GTCTCGCTCTGTAGC[C/T]CAGACTGGAGTACAG | 1161 |
rs576460104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878110 | TGTCAAACGCCTTTT[C/G]TGCATCTATTGAGAT | 1161 |
rs576469437 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928712 | TTCGATGTTTTGTAT[G/T]TACTTGAAATTAATA | 1161 |
rs576510525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60914919 | GTTGATTTATAGATG[C/T]TAAAACAACCTTTTT | 1161 |
rs576560045 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60903336 | AGAATATTAAATAAT[A/G]CATATGAGACAAGTA | 1161 |
rs576599982 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911614 | ATCCCACTTGTCAAT[A/T]TTGACTTTTGTTGCC | 1161 |
rs576618462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60892766 | GGCTGGAGCATCCAG[C/T]AGCCGGATGAACTTG | 1161 |
rs576679232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60893250 | CCTTCATAGTGGCCT[C/T]GTCATCCAGCTGAGG | 1161 |
rs576737643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60938862 | AACCTTAAATCTTAC[C/T]TTACCTAATATTCGT | 1161 |
rs576744333 | in-del | -/TA | 0.00119832 | 0.0244484 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919354 | AACTCTCCAATCTTG[-/TA]TATGTTTGAAATTTC | 1161 |
rs576748688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60880194 | TGTTGAATATTGGCC[C/T]CCACTCTCTTCTGGC | 1161 |
rs576781168 | in-del | -/AAAAAT/AAAAATAAAAAT | 0.330924 | 0.27232 | intron-variant | ERCC8 | GRCh38.p7 | 5:60886715 | CAAAAAAATAAAAAT[-/AAAAAT/AAAAATAAAAAT]AAAAATAAAAATAAA | 1161 |
rs576785211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60929909 | ATTCATTATTGATTA[A/T]AATAATGCTAGTTTA | 1161 |
rs576813285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875306 | GTTCAGTAAAACATG[C/T]AAAATACGTCAGAAA | 1161 |
rs576875901 | in-del | -/C | 0.437542 | 0.165312 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944727 | CCCACCCCCGGGGAA[-/C]CCCCCCCCACCCCCG | 1161 |
rs576880853 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ERCC8 | GRCh38.p7 | 5:60875886 | TATTTTAATTTATTT[A/C]TTTTTTCTTTTTTTT | 1161 |
rs576959093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899779 | TAGGACAATGACTGT[A/G]CCCCTCACCCACCTT | 1161 |
rs576969237 | snp | A/C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934213 | ACTGGCAGTGGAAAA[A/C/G]TGTTCCCTTTTCACC | 1161 |
rs577134348 | snp | A/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874368 | GACTTGTGTTACTTG[A/T]ACTGTAGCAATGAGG | 1161 |
rs577136788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60936254 | ATCTAGGAGGGTTGC[A/G]TATTTCCAGGAATTT | 1161 |
rs577174256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60906193 | GAGACCAGGTTATGA[A/G]ACTGGCTAATTTTTG | 1161 |
rs577197597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60937086 | GCTACTGGGGTCTGG[C/T]TGGTACAGGGCAGTT | 1161 |
rs577294403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899340 | TTGAATATGTATAGT[A/T]GGCCTCAATGGAGCA | 1161 |
rs577319337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60926810 | CAGATGTATTATCAA[C/T]ATAAAACAAAATTAT | 1161 |
rs577355657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60878737 | TTATCATTTTTTTTG[C/T]GTCTATTTGATTCTG | 1161 |
rs577368284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60931821 | ATGTATAAAGGTAAT[C/T]ATCTTTTCCTTCAGC | 1161 |
rs577379612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60927566 | TTCCCATATTTCTCA[C/G]CAACTCTGCCAACTG | 1161 |
rs577477642 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873717 | CCCTCAACAACTGTT[G/T]ACTTTTGGTATTCAA | 1161 |
rs577501812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60883596 | AGGATATTTCTTGAT[A/T]ACTTTCAAATTTCTG | 1161 |
rs577589005 | snp | C/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919334 | TGATACACAGGTCAT[C/T]ATACAACTCTCCAAT | 1161 |
rs577589207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920180 | CTATCCTGACTTCTT[C/T]TGTTTTCTGCTCATT | 1161 |
rs577615922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944168 | CTTTTTGTCATTCAC[C/G]TATCCACTCAATTTC | 1161 |
rs577654450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60920993 | TCTAAGTTCTAGAGT[A/G]TTTGAGGCGATATCT | 1161 |
rs577656121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC8 | GRCh38.p7 | 5:60913556 | CTGCTCCTGGATTCA[C/T]TGATTTTTTGAAGGG | 1161 |
rs577715723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902610 | AAGTGAGGCCAAATA[A/T]TCAATGTGAATAGAT | 1161 |
rs577778078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903401 | GAAATAACACAAGGT[G/T]TTGAGTTAGAACTAT | 1161 |
rs577781756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60924158 | TGACTGCATTCATGT[C/G]CTATAATTTAAAATA | 1161 |
rs577818143 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60876816 | TTGCAAAAATTTTCT[A/C]CCATTCTGTAGGTTG | 1161 |
rs577870442 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882137 | TGAGCCACTGCGCCC[A/G]GCTTAGAAACATTTT | 1161 |
rs577883421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60909071 | TGCCAGATAAAGATG[A/G]TTTGATAATTTTTGG | 1161 |
rs577896600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60881378 | GAGAACCACTATTCT[A/C]TTCAAAGCTGTCAGA | 1161 |
rs577899005 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917917 | ATAGTATTTTTCACA[A/G]AGGGATAATAATATT | 1161 |
rs577933591 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60887138 | TGAGGAATTTTATGT[C/T]CTTCTTTTGATATTT | 1161 |
rs577961608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60894279 | GTGAGCCACTGCGCC[C/T]GGCTGGGAATTTATC | 1161 |
rs577969594 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC8 | GRCh38.p7 | 5:60882390 | CCAAATGTCCAGAAG[C/T]GAAACTATTATTATT | 1161 |
rs577985548 | snp | C/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917133 | TTATAGCTGAAGAGA[C/G]CTTTGCTAACAAATT | 1161 |
rs578029369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC8 | GRCh38.p7 | 5:60910133 | ATTTTCAACTGTGAT[G/T]GGGGTCAGCTTCCCT | 1161 |
rs578065111 | in-del | -/AAAAA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909244 | AAATGCCCTATTCTG[-/AAAAA]AAAAAAAAAAAAAAA | 1161 |
rs578114086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887338 | ACTATAGGTGCATGC[C/T]ACTGGCAAGAAATGC | 1161 |
rs745361571 | snp | A/T | 3.32182e-05 | 0.00407529 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898452 | GTATTCAGGACATAT[A/T]TAATGTTTGATGATA | 1161 |
rs745385037 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940396 | AATCCCTGTTGTTTA[C/T]TGCCTCTCTTCTCAC | 1161 |
rs745410054 | in-del | -/G | 1.6582e-05 | 0.00287936 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945043 | GGAGCACTGGACGTC[-/G]GCCATGACAGAGCTC | 1161 |
rs745416139 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892462 | GCAGAGTGTGAGTGG[A/G]TGGTGGTGGTCTATA | 1161 |
rs745462483 | in-del | -/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945672 | AAGGCGCACCACCAC[-/T]TTTCCTCCCAGCCAC | 1161 |
rs745481102 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939607 | CTCGTGCCTCAGCCA[C/T]GTGAGTAGCTGGGAT | 1161 |
rs745486269 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897004 | GCAGGGCCCATATGA[G/T]CTGGCACCCTAGTTC | 1161 |
rs745588302 | snp | C/G | 1.74677e-05 | 0.00295526 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945279 | GTCTCAGGATTTGTT[C/G]CGCGCCTTGTGGAGA | 1161 |
rs745640235 | snp | C/T | 1.64795e-05 | 0.00287045 | missense | ERCC8 | GRCh38.p7 | 5:60887447 | ATATTTACCTCATCA[C/T]CATCAGGAACTGGTT | 1161 |
rs745663396 | snp | A/C | | | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60903178 | TTTTCATTGTTTAGA[A/C]TTAGACAATCTAATA | 1161 |
rs745683753 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913946 | AATTTGATTTCACTG[C/T]GGTCTGAGAGAGTTT | 1161 |
rs745699331 | snp | C/G | | | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903413 | GGTTTTGAGTTAGAA[C/G]TATTTTTCATATTGT | 1161 |
rs745763079 | snp | A/G | 1.65192e-05 | 0.00287391 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922118 | AGTTCTCAAGGTCAT[A/G]AAGTACAATCACACC | 1161 |
rs745771737 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927913 | AAAGTGGAAGTTTAT[C/T]AAATCTGTTCTGACT | 1161 |
rs745798827 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912891 | TTATGTGATGGATTA[C/T]GTGTATTGATTTGCC | 1161 |
rs745866167 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891634 | TTTTTTGGGGAGGGG[A/G]TAATGATATTTTTTG | 1161 |
rs745927528 | snp | C/G | 0.00023147 | 0.0107555 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945033 | TCACACCGGCTGGAG[C/G]ACTGGACGTCGCCAT | 1161 |
rs745966031 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943931 | ACATTGAAAACGTAA[A/T]GGATAAAATGTTGGA | 1161 |
rs746056140 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882753 | TACACTTATTTGCAA[C/T]AGTTGTATACTGAAG | 1161 |
rs746089510 | snp | A/C | 2.11858e-05 | 0.0032546 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874702 | AAAAAAAAAAAGATA[A/C]AGAAAAAGGAAGATT | 1161 |
rs746110609 | snp | C/T | 1.70371e-05 | 0.0029186 | intron-variant, missense | ERCC8 | GRCh38.p7 | 5:60903627 | TCAAAGTAGTTGCCG[C/T]TTGAAATAAAATAAA | 1161 |
rs746120563 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915015 | GGATTTTTGTTATTT[A/T]TATTTGTAAGAGACA | 1161 |
rs746122533 | snp | C/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945927 | CCGGCGCTGGCCCCA[C/T]GCGCCTTCCTTACTA | 1161 |
rs746136528 | in-del | -/AA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938349 | ATAGCTACCTTTTTG[-/AA]TTTTTTTTTTTTTTT | 1161 |
rs746153976 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938112 | TTTTTTTTAGGTTAC[G/T]AAGTTTCATTGAATA | 1161 |
rs746165545 | snp | C/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918481 | TAGTCTCAGGTAGGA[C/T]GATATGAATGGCCAA | 1161 |
rs746166960 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901694 | TACCCTCCACCCTCA[C/T]CTGGATCCTTGATAC | 1161 |
rs746170694 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937517 | AGGCCAATGGAGTTA[C/T]GTTCCCAGGGGGATT | 1161 |
rs746217955 | snp | A/C/G | 3.30985e-05 | 0.00406797 | stop-gained, missense | ERCC8 | GRCh38.p7 | 5:60890962 | GTTATCTGTTCTCCT[A/C/G]AGTAAACTGTATAAA | 1161 |
rs746255328 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917421 | GAATGCCAGGCTGAG[A/T]TTAGACAATGGGAAT | 1161 |
rs746400113 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893905 | CCATCTCTAGAACTC[C/T]TCATCTTGCAAAATT | 1161 |
rs746417266 | snp | C/G | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944987 | CCAAACCCGTTTGGC[C/G]TGCGGACAAAAACCC | 1161 |
rs746542192 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927937 | TCTGACTTGACTTAA[C/T]GTATTAATAATAATA | 1161 |
rs746566007 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882203 | CATTTTCCTTTTGAT[C/G]AATATGATAACTTTG | 1161 |
rs746622718 | snp | A/G | 1.6569e-05 | 0.00287824 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928837 | CACTTAGAAAGAAAA[A/G]TGATTATACAAGTAT | 1161 |
rs746630537 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926770 | TCGTAATTAATCTTC[A/G]TGAAACGTTGCTTTT | 1161 |
rs746632112 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942189 | GAAAGGGGAAACATA[A/G]ATATGGAGCAGCTAG | 1161 |
rs746662773 | snp | A/T | 1.65228e-05 | 0.00287422 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898409 | GTGTTTGCTGCAATG[A/T]AAAACATAGTTCAGT | 1161 |
rs746720196 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940611 | CATCCCTGAGTGAGG[C/T]ATGCATAGATCTAAC | 1161 |
rs746812858 | snp | A/C | 1.65211e-05 | 0.00287407 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902538 | ATATGAAAAGTCTTG[A/C]AAGATATCTGAAAAA | 1161 |
rs746863787 | snp | C/T | 1.77432e-05 | 0.00297847 | missense | ERCC8 | GRCh38.p7 | 5:60874683 | GTGATTTTGTTGTAG[C/T]CTAAAAAAAAAAAAG | 1161 |
rs746876980 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875668 | ACTCTTAAATTATTT[C/T]AGATTTATTGCCTTT | 1161 |
rs746894753 | snp | A/G | 1.68627e-05 | 0.00290363 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945439 | GCGAGGTCAGTAAAG[A/G]AGGGAAAAGTGAGAG | 1161 |
rs746905935 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915033 | TTTGTAAGAGACACT[A/G]GCTTGTAATTTTCCA | 1161 |
rs746991834 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914760 | CCACTGCACTCTAGC[G/T]TGGGGAACAGGGCAA | 1161 |
rs747126236 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932143 | CAGGACTGAATTGTC[C/T]GTGAACTAGAAGGAG | 1161 |
rs747208043 | snp | A/C | 6.61201e-05 | 0.00574941 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902435 | AAGCAAATAAGTTAA[A/C]TTTTACCTTGCTGTT | 1161 |
rs747219639 | in-del | -/TTA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938087 | ATATATATATATATT[-/TTA]TTATTTTTTTTTTTT | 1161 |
rs747243717 | snp | A/G | 1.64988e-05 | 0.00287213 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945025 | TCGTGTCCTCACACC[A/G]GCTGGAGCACTGGAC | 1161 |
rs747271093 | in-del | -/A | | | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874553 | TAGACCATACAGTTG[-/A]AAAAAAACACAGTCT | 1161 |
rs747271975 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878079 | AGAGTTTTTAGCATG[-/A]AAGGTTGTTGAATTT | 1161 |
rs747290927 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905422 | CCAGCTTGGATTTCA[A/G]GGTCCAATACCAATA | 1161 |
rs747302125 | snp | A/G | 1.65362e-05 | 0.00287538 | upstream-variant-2KB, synonymous-codon | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945342 | CACGGACCAATTCGG[A/G]AACAAATACTACTAC | 1161 |
rs747315380 | in-del | -/TCTAATGAGCT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932501 | CTTCAACATTGAGTC[-/TCTAATGAGCT]TCCCTGATAGACATT | 1161 |
rs747315891 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890478 | CTTCAAAACCTCCCT[A/T]TACTAGCCATTGGTA | 1161 |
rs747422895 | snp | C/T | 1.66203e-05 | 0.00288268 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918237 | CTTTATCCTACAAAG[C/T]AATCTGCAAATGTTT | 1161 |
rs747430346 | snp | C/T | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919762 | GCCAGGTGTGGTAAC[C/T]AAATCAACTTAGGAT | 1161 |
rs747477380 | snp | A/T | 3.30836e-05 | 0.00406702 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887565 | TGGATCAAGAGCTGA[A/T]ATCAAACTGAAATGA | 1161 |
rs747523089 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896562 | GCAGGACTGGTTCTA[C/T]CTGATAGCCCTTTAA | 1161 |
rs747530954 | snp | C/T | 1.656e-05 | 0.00287745 | missense | ERCC8 | GRCh38.p7 | 5:60890945 | AATGTCCCTTAAGCA[C/T]AGTTATCTGTTCTCC | 1161 |
rs747535326 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933105 | GCTTGCCCAAATTTC[C/T]TATTTAATTTCAGTT | 1161 |
rs747558306 | in-del | -/TT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891765 | AGCCTCTTGGGACTC[-/TT]TTTCCTGGAGAGAGT | 1161 |
rs747559514 | in-del | -/AA | 1.64868e-05 | 0.00287109 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904748 | CATATAAAAAGGGAG[-/AA]AGTTTTCAGTATGTC | 1161 |
rs747609539 | snp | G/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946404 | TATAAAATGTATTCT[G/T]TGATTTATCACTCAA | 1161 |
rs747670539 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901617 | AAAGTTAACTGTATT[A/C]ATGTCCACCTTTTCC | 1161 |
rs747710344 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888805 | AATTCAGTGTATTTT[C/T]CCTGTGAACAAGGGT | 1161 |
rs747729199 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929815 | TTGTAAGTATCTAGC[A/G]AATATTAACTATTTG | 1161 |
rs747764419 | snp | C/T | 3.33061e-05 | 0.00408068 | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918415 | CAATCAAAATTTACA[C/T]TAACTGACTTATGTG | 1161 |
rs747823137 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908699 | GAAGCAGAGAAAAGT[A/C]ATGACATTATAAAAA | 1161 |
rs747827126 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894904 | TCGGCTGGGCGTGGT[C/G]TCACTCCCGTAATCC | 1161 |
rs747828729 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60903960 | TGAAATAATTATAGA[-/T]TTGCAAGCAGTTGCA | 1161 |
rs747885140 | in-del | -/AA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60874686 | ATTTTGTTGTAGTCT[-/AA]AAAAAAAAAAGATAA | 1161 |
rs747901558 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60928106 | TAATGCTATATGTGG[C/T]CTAATTGTAGGCCAC | 1161 |
rs747942972 | snp | C/G | 3.29462e-05 | 0.00405857 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944959 | TCTGCTCTCCGAAGG[C/G]GAAGAGGGTCCTCCA | 1161 |
rs747957752 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924018 | AAAAATTTTAATGTC[A/T]TTTAACTTTAAGCTA | 1161 |
rs747959708 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939186 | ATTCATTTCCATCTT[A/G]TCAATTGAGAAGTGT | 1161 |
rs748107555 | snp | A/C | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919870 | TTTTTAAAAAACAGT[A/C]ATTATGGGAAGAAAG | 1161 |
rs748157270 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899978 | ACAAAATTTTGCTGC[A/T]TTTTATATTGTTTTA | 1161 |
rs748188210 | snp | A/C | 1.65252e-05 | 0.00287443 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945358 | AACAAATACTACTAC[A/C]TCCCGCAGTACAAGA | 1161 |
rs748193470 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905666 | GTCATAGACAACAAA[C/T]GAACATATTGTAACT | 1161 |
rs748218049 | snp | C/G | 8.28864e-05 | 0.00643711 | missense | ERCC8 | GRCh38.p7 | 5:60890933 | CAACAGTTTTATAAT[C/G]TCCCTTAAGCATAGT | 1161 |
rs748251944 | in-del | -/GCAA | 0.000241325 | 0.010982 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890843 | CATATAACTGGTCTG[-/GCAA]GCAAGCTAGCTAGCT | 1161 |
rs748332066 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891942 | CAATTAGTTACCAAC[A/G]CTGCCATCAGCATTG | 1161 |
rs748379243 | snp | C/T | 1.65855e-05 | 0.00287967 | splice-acceptor-variant | ERCC8 | GRCh38.p7 | 5:60928961 | CCAGTCCCAAAACTC[C/T]TAAAAATAAAAGGGG | 1161 |
rs748421359 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897479 | AGCACAGTATCTGAC[A/G]TACAAGCTCTCAATA | 1161 |
rs748481426 | in-del | -/AC | 1.64836e-05 | 0.0028708 | frameshift-variant, intron-variant | ERCC8 | GRCh38.p7 | 5:60904825 | TGGTGGAGACTGGAG[-/AC]ATATGATGACTATAA | 1161 |
rs748482628 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892384 | GTCTTCATTGACTTG[C/T]TCGGTATCCTCGATG | 1161 |
rs748572093 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914575 | GTGGGAGGATCATTT[C/G]AGGCCAGATTTTGAC | 1161 |
rs748612232 | snp | C/T | 5.35776e-05 | 0.00517551 | upstream-variant-2KB, synonymous-codon | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945261 | GGTGGACGGCATGGG[C/T]TGGTCTCAGGATTTG | 1161 |
rs748614275 | snp | C/T | 1.65466e-05 | 0.00287628 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60903676 | AGAACAGGATCCAGA[C/T]TTCAAGTCACAAAGT | 1161 |
rs748646383 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883819 | CTTGTCTTGACCAGA[C/T]CAGCTTTTAGAAAGG | 1161 |
rs748672570 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60921297 | GGAAGAGCTGTAATA[A/G]ATAGTTGATGTTAAT | 1161 |
rs748686983 | in-del | -/GGC | 4.95987e-05 | 0.00497965 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945390 | CTGGAGAGGTGAGGT[-/GGC]GGCGTGGGCAGCGAT | 1161 |
rs748762631 | snp | C/T | | | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903562 | ACATTAGTCATGTCA[C/T]TTACAAAGAATACAC | 1161 |
rs748767620 | in-del | -/TTT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884524 | TATGTGTGTATGTGT[-/TTT]TTTTTTTTTTTTTGT | 1161 |
rs748807233 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889891 | TACCTTCTTATTGAC[G/T]AATAAAAAGAGATAC | 1161 |
rs748834100 | snp | C/T | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873366 | GATAGGAGGTCTAAC[C/T]CTTATACACTTAAAA | 1161 |
rs748835328 | in-del | -/TT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893985 | TCCTGGGAATTTATC[-/TT]TTTTTTTTTTTTTTT | 1161 |
rs748843229 | snp | A/C | | | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874110 | AGCATGGTTAATTAA[A/C]TGAAACCACTGAAAA | 1161 |
rs748850986 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931517 | TATTGCTATGTTGCC[C/G]AGGCTGGTTTGGAAC | 1161 |
rs748857897 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929770 | AAATGAGTTTGTATA[G/T]AAAAGGTGCTAATTA | 1161 |
rs748871386 | in-del | -/AGA | 1.65446e-05 | 0.00287612 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902556 | GATATCTGAAAAATC[-/AGA]AGATAAAGTGCCAAT | 1161 |
rs748873998 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917032 | AGTAAAATAATGGTT[A/G]ATATTTACTCCAGAA | 1161 |
rs748885030 | snp | C/G/T | 3.30563e-05 | 0.00406538 | upstream-variant-2KB, stop-gained, synonymous-codon | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945354 | CGGGAACAAATACTA[C/G/T]TACATCCCGCAGTAC | 1161 |
rs748912351 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911140 | TAGGTATATATGTGC[C/T]ATGTTGGTTTGCTGC | 1161 |
rs748953999 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896164 | CTAATTTTGTACTTT[C/T]AGTAGAGATGGGGTT | 1161 |
rs749009663 | snp | C/T | 1.66913e-05 | 0.00288883 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945425 | CGTGGTCAGTGATTG[C/T]GAGGTCAGTAAAGGA | 1161 |
rs749030668 | snp | A/G | 1.65941e-05 | 0.00288041 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918259 | CAAATGTTTTAATGT[A/G]CTTACTTGTAATGTA | 1161 |
rs749063501 | snp | C/T | 1.65206e-05 | 0.00287403 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928861 | CAAGTATAATAAACT[C/T]ACTATCTCCCTTCAA | 1161 |
rs749187470 | snp | C/T | 1.6517e-05 | 0.00287372 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928939 | ACATCTCTGTCTTTA[C/T]TTAATTCCAGTCCCA | 1161 |
rs749202399 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901629 | ATTCATGTCCACCTT[C/T]TCCTCTTTCCATTTA | 1161 |
rs749231246 | in-del | -/TCAG | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881150 | CCGTTTGCCTGGCTA[-/TCAG]TCAGCTCAGAGACTG | 1161 |
rs749238707 | snp | A/T | 3.29864e-05 | 0.00406105 | missense | ERCC8 | GRCh38.p7 | 5:60899706 | TCTTCTCACATCCCA[A/T]AATTTTACTCTACTG | 1161 |
rs749284118 | in-del | -/GT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926344 | TAGCTCCTTTAAATG[-/GT]GTGTGTAATGATGTA | 1161 |
rs749292326 | snp | A/C | | | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60902877 | GTTTTCCAATTTCTC[A/C]TAAAGTTATAAGAGA | 1161 |
rs749293950 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888964 | TGCTGCACTTAGTCG[C/T]CAAGTCTCTTTAGTT | 1161 |
rs749326705 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935572 | GGACTTCCAGCACTA[C/T]GTTGAATAGAAGTGG | 1161 |
rs749484372 | snp | A/G | 3.29837e-05 | 0.00406088 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887534 | TCCTATAACATAGAA[A/G]GCAAAGATGATACTG | 1161 |
rs749569622 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881737 | GGGTGGGAGTGACCC[A/G]ATTTTCCAGGTGCCG | 1161 |
rs749582731 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935057 | ATGCAGGCTCTTTTT[G/T]CCTAGTTCTGTGAAG | 1161 |
rs749613854 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911623 | GTCAATTTTGACTTT[G/T]GTTGCCATTGCTTTT | 1161 |
rs749656923 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885371 | CATCCTTTTCTATAC[A/G]TAAGTCACTATAGAT | 1161 |
rs749696593 | snp | C/G | 1.65499e-05 | 0.00287657 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945038 | CCGGCTGGAGCACTG[C/G]ACGTCGCCATGACAG | 1161 |
rs749713815 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909809 | AAATACAAAAATTAG[A/C]CAGGCATGGTGACAC | 1161 |
rs749761409 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943856 | AAGGCTGATGATGTG[C/T]CAGAGGAAGTGACAC | 1161 |
rs749864520 | snp | A/C | 1.73586e-05 | 0.00294601 | upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945084 | CTGGAACAGCAGAGT[A/C]TCCCATTGGTCAGTC | 1161 |
rs749887921 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889357 | ATATTCTGTTGCCCA[C/T]GTTGGAGTGCAGTGG | 1161 |
rs749907718 | snp | C/T | 1.65067e-05 | 0.00287282 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928927 | TGGATTCTTTCAACA[C/T]CTCTGTCTTTATTTA | 1161 |
rs749988724 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916439 | CTGATTCTCAATTCC[C/T]AGATTTCTTGGCAGC | 1161 |
rs750051495 | snp | C/T | 3.33678e-05 | 0.00408446 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902394 | GTAGACTTTTCAAAA[C/T]GCTTATTATTAATTA | 1161 |
rs750129971 | in-del | -/GAAGAGGCCCC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931849 | GCTCCCTCTTCCTAA[-/GAAGAGGCCCC]CAGTAAGAAGCATGG | 1161 |
rs750224072 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884626 | AAAGCACTTTTAAAC[A/T]TGGCTTAAATTATAA | 1161 |
rs750236083 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905727 | AACAAAATCAATTCA[C/T]AAAAACCATGGCATT | 1161 |
rs750242117 | snp | A/T | 1.68599e-05 | 0.00290338 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903763 | TATCATAAGTCATCA[A/T]CAAAAGGAAACAAGA | 1161 |
rs750277505 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934248 | CCATGCCAACATCTA[C/T]TATATTTTGATTTTT | 1161 |
rs750280997 | snp | A/G | 8.24328e-05 | 0.00641947 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887523 | CACTATAAAGTTCCT[A/G]TAACATAGAAGGCAA | 1161 |
rs750293312 | snp | C/T | 5.00396e-05 | 0.00500173 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904893 | TAATCAAAAGACATT[C/T]AAAAAGTATAAGGTT | 1161 |
rs750353658 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931302 | AACTTTAACATTAAA[-/T]TTTTTTTTTAAATTT | 1161 |
rs750421412 | in-del | -/AAAAAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886704 | GAGACTCCATCTCAA[-/AAAAAT]AAAAATAAAAATAAA | 1161 |
rs750457709 | snp | C/G | 9.9054e-05 | 0.00703685 | missense | ERCC8 | GRCh38.p7 | 5:60898391 | ACTTTCCCATTATGA[C/G]CAGTGTTTGCTGCAA | 1161 |
rs750459388 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925902 | GATCTCGGCTCACTG[A/C]AACCTCTGCCTCCCA | 1161 |
rs750482217 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60874833 | ATTTCAGAACAAAAA[C/T]AAGAAACAACCCATA | 1161 |
rs750536447 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912494 | AAGAGATTTTGGGCT[C/G]AGACGATGGGGTTTT | 1161 |
rs750573888 | snp | C/G | 3.40866e-05 | 0.00412822 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945069 | AGCTCAGGGGCGGGA[C/G]TGGAACAGCAGAGTC | 1161 |
rs750586154 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938748 | CCACTTAAGGGATGT[A/G]AAGTCATGTATCTAC | 1161 |
rs750602829 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944150 | ATCATTATTCATTCT[-/TC]TCTTTTTGTCATTCA | 1161 |
rs750622098 | in-del | -/T | 1.64787e-05 | 0.00287038 | frameshift-variant | ERCC8 | GRCh38.p7 | 5:60887466 | AGGAACTGGTTCATA[-/T]TAAGGATGGAACCCA | 1161 |
rs750654667 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883537 | TTTAGAGGGGACCTA[A/G]TTATGAGTTTAGAGA | 1161 |
rs750683761 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907966 | TAGCATTCAACACAA[C/T]TGATTACTCCCATCC | 1161 |
rs750685730 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60880185 | TTTAAGAATGTTGAA[-/T]TATTGGCCCCCACTC | 1161 |
rs750720768 | snp | C/T | 4.8998e-05 | 0.0049494 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874721 | AAAAGGAAGATTCTG[C/T]TTTTTCTACTTCATA | 1161 |
rs750752486 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902653 | CAGATTTATAATAAT[C/T]GATGTTTCAATGCTA | 1161 |
rs750782363 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888602 | TGACTAACAAAGAAC[A/C]CTTAGATAGAATGAT | 1161 |
rs750784813 | in-del | -/AA/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898794 | CTAGTGTTTTCCATT[-/AA/G]GAAAAAAAAAACAGG | 1161 |
rs750840622 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889608 | GCGCAGCCATTGTCA[C/T]GATTTTAATCCATTC | 1161 |
rs750856998 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896247 | TTGAGACGGAGTTTT[C/G]CTCTTGTTGCCCAGG | 1161 |
rs750865312 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913657 | ATTTGTTTGCTCTTG[C/T]TTCTCTAGTTCTTTT | 1161 |
rs750890824 | in-del | -/TAAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909975 | AGAAAAAAAAAAAAA[-/TAAT]AATAATAAAAGAATA | 1161 |
rs750899599 | snp | C/T | 1.80065e-05 | 0.00300049 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922181 | AAAAGTTCACATTAA[C/T]TTATCATTTTATTTA | 1161 |
rs750915339 | snp | G/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946204 | CAGAAAATGTCAGGT[G/T]TTGGGCGAAGAGGCG | 1161 |
rs750952126 | snp | A/G | 1.66576e-05 | 0.00288592 | missense | ERCC8 | GRCh38.p7 | 5:60898277 | TAAAAATCTCTTACA[A/G]GTGTGTTTTCTCCAT | 1161 |
rs750960035 | snp | C/T | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873716 | ACCCTCAACAACTGT[C/T]TACTTTTGGTATTCA | 1161 |
rs751022131 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881620 | CAGACTGCTGTGCTA[A/G]CAATGGGCGAGGCTC | 1161 |
rs751056695 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883674 | TTGACACAAGTGATA[C/T]GTAAAACAGTTATGT | 1161 |
rs751058816 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895602 | GGTATTCAGTAAGTT[A/C]CTAGATTAATTCCTA | 1161 |
rs751073213 | snp | A/G | 1.64849e-05 | 0.00287092 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60887515 | TCTGCTACCACTATA[A/G]AGTTCCTATAACATA | 1161 |
rs751074191 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941941 | AGTATATAATGTATG[C/T]AAATATAAAATATAA | 1161 |
rs751133811 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943389 | ATTAACCGTGAGAAA[C/T]AGCATAAAAGTTTGC | 1161 |
rs751159291 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882042 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 1161 |
rs751173329 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925418 | TGGTTAGCTCTTTGG[-/A]AAGATATTAGAGTCC | 1161 |
rs751218348 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923059 | CAGTGTGGAAGGGAA[A/G]GAGTGGTGAGAGATG | 1161 |
rs751311543 | in-del | -/TTCAG | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905285 | TTTGAAATCATACAT[-/TTCAG]TTCAGTTATCTATGA | 1161 |
rs751348349 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918023 | CTCACAACCATACTA[C/T]AATCATTATTCCCAT | 1161 |
rs751393209 | snp | C/G | 5.07825e-05 | 0.00503872 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945063 | TGACAGAGCTCAGGG[C/G]CGGGACTGGAACAGC | 1161 |
rs751446486 | snp | G/T | 2.01986e-05 | 0.00317787 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945219 | TACCCCTACTGCGGG[G/T]CCCGCTGCTGGCAGC | 1161 |
rs751452995 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907841 | ATCTCTAATTCCTTA[C/T]CTCCCACGTATTTCT | 1161 |
rs751453214 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893131 | CCCATAGGATAGCCT[C/T]CCCCATTTGGAAGCA | 1161 |
rs751477337 | in-del | -/AC | 1.75775e-05 | 0.00296453 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874591 | AAAGTTTCAGCAGAG[-/AC]AAAAAGGTACTAAAG | 1161 |
rs751478627 | snp | C/T | 3.29641e-05 | 0.00405968 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887433 | CATTTGTGAAAATAA[C/T]ATTTACCTCATCATC | 1161 |
rs751490973 | in-del | -/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942197 | AACATAAATATGGAG[-/C]CAGCTAGCACTCTCA | 1161 |
rs751504293 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885704 | AGATTTATCAAAAGG[C/T]ATTTTTTTCTCTTTA | 1161 |
rs751605264 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913746 | GTGCTATAAATTTCC[C/G]TCTATATACTGCTTT | 1161 |
rs751610285 | in-del | -/A | 1.69272e-05 | 0.00290918 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898263 | CCCAAATATATACTT[-/A]AAAATCTCTTACAAG | 1161 |
rs751639405 | snp | A/G | 1.67276e-05 | 0.00289197 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60891047 | AGACAGTGAATTTCA[A/G]TCCTTTTTTACTGTT | 1161 |
rs751658616 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897794 | TTTTGGATTTTAGAA[C/T]ATTTGCTTTACTGCC | 1161 |
rs751676332 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927396 | TAATGCAAAATACAA[A/G]TCTTAGCAAACAATG | 1161 |
rs751679544 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899371 | AAAACAAAACAAGTA[A/G]AGCAAGTTAATTCAC | 1161 |
rs751702279 | in-del | -/AAATAAAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906731 | AAAACTCTGTCTCAA[-/AAATAAAT]AAATAAATAAATAAA | 1161 |
rs751766342 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941367 | ATCCATTAAAATTAT[A/G]CAATCTAACAATATA | 1161 |
rs751847577 | in-del | -/GT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933496 | GTGCTGGGATTACAG[-/GT]GTGAGCCACCATGCC | 1161 |
rs751860037 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893025 | GCCACAGTTGGCAAC[G/T]CATTCCGAAGGTAAT | 1161 |
rs751900687 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935845 | TGTATCACCTTTATG[G/T]ACTTGCATATGTTAA | 1161 |
rs751942615 | snp | A/G | 4.94776e-05 | 0.00497357 | missense | ERCC8 | GRCh38.p7 | 5:60902472 | ATATAGTCATAACGT[A/G]GAGACCAGGAAACTG | 1161 |
rs751974161 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912576 | TTCCTAATTGAATAC[C/G]CTTTATCTCTTTCTC | 1161 |
rs752023359 | snp | C/T | 1.80631e-05 | 0.0030052 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945472 | CCTAGTCAACTAACG[C/T]ATCATGCGACACTTA | 1161 |
rs752054337 | snp | C/G | 1.65463e-05 | 0.00287626 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945398 | GTGAGGTGGCGGCGT[C/G]GGCAGCGATTGCGTG | 1161 |
rs752083251 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934739 | TTGAGTTGATTTTTG[C/T]AGAAGGTGAGAGATG | 1161 |
rs752087015 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932525 | CTTCCCTGATAGACA[C/T]TTCACATATGTTGTC | 1161 |
rs752132183 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917837 | TACAGTATTAACAGC[A/T]TTCTCCTTCAAGTTT | 1161 |
rs752198415 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939369 | TGATTAACGTTCTTT[C/G]CTAATTTTTTTCCTG | 1161 |
rs752236421 | snp | A/T | 2.10928e-05 | 0.00324745 | intron-variant, missense | ERCC8 | GRCh38.p7 | 5:60903599 | TAACGTTTCTTTTTA[A/T]TGAATCGTTTACTCA | 1161 |
rs752281244 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931472 | TTACCACACCTGGCT[A/C]AGTTTTGGTATTTTT | 1161 |
rs752371511 | snp | C/T | | | upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945107 | GGTCAGTCGGTGATA[C/T]ATCCGGCCAATGGTG | 1161 |
rs752440832 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889740 | AAGAAAGGAGGGACA[A/C]TGTTTTAAGAATTTC | 1161 |
rs752442112 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904237 | CTCAAGACAACTTAG[C/T]TCCTAGCTCTTCTTC | 1161 |
rs752454170 | in-del | -/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60880793 | CAAGGTTTTTAACTT[-/C]TTTGCCATGGGTTCA | 1161 |
rs752467141 | in-del | -/AAAT | 1.65112e-05 | 0.00287321 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899736 | GTCAGCACTGAGAAG[-/AAAT]AAATGTTACATTGAC | 1161 |
rs752526268 | snp | C/G | 3.29576e-05 | 0.00405928 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945012 | AAACCCCAGCATATC[C/G]TGTCCTCACACCGGC | 1161 |
rs752578295 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895756 | TTCACTGTTCCCCCT[A/G]GAAAAATTATAAACT | 1161 |
rs752624814 | in-del | -/T | 2.03643e-05 | 0.00319088 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922200 | TCATTTTATTTATTA[-/T]TTAGTCCATTTATTT | 1161 |
rs752683992 | snp | A/T | 4.99646e-05 | 0.00499798 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945050 | CTGGACGTCGCCATG[A/T]CAGAGCTCAGGGGCG | 1161 |
rs752754862 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936020 | TCTTTCCTGGTTTTG[A/G]TATTAGCATGATATT | 1161 |
rs752757232 | snp | A/G | 3.29875e-05 | 0.00406112 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60899708 | TTCTCACATCCCATA[A/G]TTTTACTCTACTGTC | 1161 |
rs752764592 | snp | C/G | 1.65367e-05 | 0.00287543 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945392 | GGAGAGGTGAGGTGG[C/G]GGCGTGGGCAGCGAT | 1161 |
rs752768220 | snp | C/G/T | 4.9876e-05 | 0.00499359 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918227 | TTAAATTCTCCTTTA[C/G/T]CCTACAAAGCAATCT | 1161 |
rs752813093 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886508 | GGAGTTGAAGACCAG[A/C]CTGACAAACATGGTG | 1161 |
rs752819668 | snp | C/T | 1.65597e-05 | 0.00287743 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918316 | ATCAAATGAGCTTGA[C/T]GTGAACATGCCAGTG | 1161 |
rs752863862 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930640 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 1161 |
rs752883762 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60928311 | GGCAACTGTTTATGA[C/T]GTGCCAGGTCTTACG | 1161 |
rs752916511 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908110 | TGTCCTATTTATCTT[G/T]GTCTTCATGGTCTTG | 1161 |
rs753050049 | snp | C/G | | | intron-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60924304 | ACCGTCAATCCTTAA[C/G]TTGCTGTCTCTCTTG | 1161 |
rs753090742 | snp | C/G | 3.30169e-05 | 0.00406293 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944902 | CAGATTCTAACTGGC[C/G]TGTTAGCCAAAAAGT | 1161 |
rs753095874 | snp | A/G | 3.29707e-05 | 0.00406008 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60899670 | ATTATGTTGATCAAG[A/G]GTAATCAAACATCCT | 1161 |
rs753102029 | in-del | -/AC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882972 | TAGCCCTGGGAAAAC[-/AC]ACACACACACACACA | 1161 |
rs753106074 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917385 | ATTGAAGGAACAAGG[A/G]TTGATGTCATGGAGA | 1161 |
rs753158647 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878865 | TTTTGTGTCTCTATT[C/T]CCTTCAGTTCTGCTC | 1161 |
rs753211772 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876329 | GTTGTGAATAGTGCC[A/G]CAATAAACATACGTG | 1161 |
rs753215899 | snp | A/C/T | 1.654e-05 | 0.00287571 | ERCC8, NDUFAF2 | 5 | allele_origin=T(germline)/A(germline) | 5:60945335 | ACGTGGGCACGGACC[A/C/T]ATTCGGGAACAAATA | 1161 |
rs753236897 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937170 | CCAGCACCGGCAACC[A/G]TAGAGGCAGCAGGGG | 1161 |
rs753276959 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942607 | AGTGACCTAAAGCAG[A/G]TTAGTAGTTTCTAGA | 1161 |
rs753293232 | snp | A/C/T | 4.9531e-05 | 0.00497629 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899614 | TCATATTTATTAATG[A/C/T]GTTCTTCCTTACCTG | 1161 |
rs753307062 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940547 | AGATCACAGAGAAGA[A/G]GGAGCTCAGGAAAGT | 1161 |
rs753378067 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934400 | TTGAGAACTGTCTAT[A/C]CATGTCAGCCCACTT | 1161 |
rs753387028 | snp | C/T | 8.23866e-05 | 0.00641767 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945010 | AAAAACCCCAGCATA[C/T]CGTGTCCTCACACCG | 1161 |
rs753396435 | snp | A/T | 3.29897e-05 | 0.00406125 | missense | ERCC8 | GRCh38.p7 | 5:60902489 | AGACCAGGAAACTGC[A/T]AATATTTCTTGTCTG | 1161 |
rs753422244 | snp | C/T | 1.66793e-05 | 0.0028878 | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918425 | TTACATTAACTGACT[C/T]ATGTGAGTTTCAAAA | 1161 |
rs753471848 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932621 | CCTGTGCCTGGTTTC[C/T]TCCACACTTTGCCCA | 1161 |
rs753481128 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905994 | GGGCCACAGGGGCAG[C/T]TGGCAGGTCCAGGTG | 1161 |
rs753492096 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891358 | TGAAGAATCATTTTA[C/G]ACCATTTAGCAAAAA | 1161 |
rs753545763 | in-del | -/G | 1.66056e-05 | 0.00288141 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928828 | ACTGCATTTCACTTA[-/G]AAAGAAAAATGATTA | 1161 |
rs753567215 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882344 | TTATTGTTAAACAGA[C/T]TACATTATTAAACTT | 1161 |
rs753661190 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896319 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGTGTCA | 1161 |
rs753663016 | snp | G/T | 4.97954e-05 | 0.00498951 | stop-gained | ERCC8 | GRCh38.p7 | 5:60890913 | TGACTGAAATACACA[G/T]CAGTCAACAGTTTTA | 1161 |
rs753690038 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941749 | AGAAACCATTAGACC[C/T]ACTCTAAAAAAATTG | 1161 |
rs753694792 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940258 | TGAAAAGTAAACAGC[C/T]ACAGACAATCCCATG | 1161 |
rs753749013 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883477 | ACCAGGTTGTCAATT[C/T]TACTGACAGATAGTG | 1161 |
rs753794410 | in-del | -/TA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937367 | GAGCTCCCAGGAGAT[-/TA]TGTCTTTTGTCTTCA | 1161 |
rs753884526 | snp | A/G | 1.89181e-05 | 0.0030755 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945232 | GGTCCCGCTGCTGGC[A/G]GCGCTGGAAACTGGG | 1161 |
rs753891428 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937461 | GATCTCCTTGGGTGA[C/G]GCTTGCCGCTGCTGC | 1161 |
rs753902917 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889479 | CCTGGCTGATTTTTT[G/T]ATTTTTTGTAAATAC | 1161 |
rs753906336 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923632 | TTACCTTAATTCAAA[A/G]TACCTTTCTTTAGTA | 1161 |
rs753909961 | snp | A/C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924707 | TGCCTATGTTCTATA[A/C/T]ATACACCTCTTGAAT | 1161 |
rs754001235 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60916090 | CTTCAAATGTCTTCT[C/G]CTTCATTTCTTAAGT | 1161 |
rs754006195 | in-del | -/AT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886959 | TAGAAATGTTTACAC[-/AT]AGTTATTAATGACAT | 1161 |
rs754095277 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895170 | GCGAGACTCTACCTC[-/A]AAAAAAAAAAAAAAA | 1161 |
rs754096373 | snp | A/G | 1.64827e-05 | 0.00287073 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904914 | GTATAAGGTTTAAGT[A/G]TAAAAACAAAGCAAT | 1161 |
rs754248915 | snp | A/C | 0.000173942 | 0.00932419 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922192 | TTAATTTATCATTTT[A/C]TTTATTATTTAGTCC | 1161 |
rs754294477 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900746 | TTAGATTTGAACATA[C/T]CCAACTTTTAACACT | 1161 |
rs754303806 | snp | C/T | 1.65198e-05 | 0.00287395 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898404 | GAGCAGTGTTTGCTG[C/T]AATGAAAAACATAGT | 1161 |
rs754351658 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899030 | TGTTTTATATAGTTT[G/T]TAAACTTTGTGATTG | 1161 |
rs754443340 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937476 | GGCTTGCCGCTGCTG[C/T]TGTGGTAGATGGGGG | 1161 |
rs754470656 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906602 | GGCGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 1161 |
rs754503105 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945015 | CCCCAGCATATCGTG[C/T]CCTCACACCGGCTGG | 1161 |
rs754513955 | snp | C/T | 1.79152e-05 | 0.00299287 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874568 | GAAAAAAACACAGTC[C/T]CATTTAAAAAGTTTC | 1161 |
rs754530979 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929622 | CAACTTAACATTTAT[A/G]TGTATTTAAATAAAG | 1161 |
rs754566666 | snp | A/G | 1.67944e-05 | 0.00289775 | missense | ERCC8 | GRCh38.p7 | 5:60874658 | GCATCTTCAAAGGCC[A/G]GATTTAATTGTGATT | 1161 |
rs754647654 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892493 | GAAGCTGATCTTCCC[A/G]CTCACCCAGTCAGCT | 1161 |
rs754677895 | snp | A/G/T | 0.000100202 | 0.00707762 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945426 | GTGGTCAGTGATTGC[A/G/T]AGGTCAGTAAAGGAG | 1161 |
rs754713736 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906873 | GCTAAAGGCAAGAGG[C/G]GGTGGTGGCTAGATC | 1161 |
rs754801852 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907860 | CCACGTATTTCTCAA[C/G]TAATTGCAATCTTAT | 1161 |
rs754847367 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908635 | TCACATTATCATACA[C/T]CTTGGAACCCATACG | 1161 |
rs754890794 | in-del | -/CTT | 1.68821e-05 | 0.0029053 | cds-indel | ERCC8 | GRCh38.p7 | 5:60874620 | AAGATGATATTCATC[-/CTT]CTTCATCACTGCTGC | 1161 |
rs754924186 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916308 | ATCTGCCTCTTAGAA[A/G]CTATCCAATGCCTGT | 1161 |
rs754931194 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944946 | CCTCCGTGTTGACTC[C/T]GCTCTCCGAAGGCGA | 1161 |
rs754947095 | in-del | -/T | 1.66918e-05 | 0.00288888 | splice-donor-variant | ERCC8 | GRCh38.p7 | 5:60898275 | TTAAAAATCTCTTAC[-/T]AAGTGTGTTTTCTCC | 1161 |
rs754949729 | snp | C/T | 3.32956e-05 | 0.00408004 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902408 | ATGCTTATTATTAAT[C/T]ACTAACTTCAAAAGC | 1161 |
rs754952354 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897986 | TCATATCTTTAATTT[A/G]TATCAGTAGTCCTCA | 1161 |
rs755014243 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931281 | ATATTTGGCTGAGCC[A/G]CATTTGAACTTTAAC | 1161 |
rs755078834 | snp | A/C/G | 0.0001325 | 0.00813849 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945317 | CAAGGGAAGTGAAGG[A/C/G]GCACGTGGGCACGGA | 1161 |
rs755117208 | snp | A/G | 1.64844e-05 | 0.00287087 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904765 | AGTTTTCAGTATGTC[A/G]AAAGACAAAAGAATA | 1161 |
rs755150165 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927525 | TGCATTTCTCAAATA[C/T]ATTTCATGCACATAT | 1161 |
rs755161772 | snp | C/G/T | 4.9522e-05 | 0.00497584 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887547 | AAGGCAAAGATGATA[C/G/T]TGTGGATCAAGAGCT | 1161 |
rs755213944 | snp | A/C | 1.65932e-05 | 0.00288034 | missense | ERCC8 | GRCh38.p7 | 5:60890915 | ACTGAAATACACAGC[A/C]GTCAACAGTTTTATA | 1161 |
rs755225081 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886403 | ATTTGACGTGAGAAC[A/C]AAGTCTTAAAAATGT | 1161 |
rs755228520 | snp | C/T | | | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874047 | AAGCCTCCTGTGATG[C/T]ACATTTTGGATAGTA | 1161 |
rs755315718 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924561 | ATATAAATCCCCCCC[-/T]CTTATATAAAGTTCC | 1161 |
rs755323194 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891155 | CAACAAAGCCTAGGA[G/T]AAATACTTAAAATAT | 1161 |
rs755389840 | snp | A/G | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919764 | CAGGTGTGGTAACTA[A/G]ATCAACTTAGGATCA | 1161 |
rs755392773 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875314 | AAACATGCAAAATAC[A/G]TCAGAAATGGTAACA | 1161 |
rs755405622 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911562 | TTCACTTAATGGTAG[-/T]TTCTTTTGCTGTGCA | 1161 |
rs755431677 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892057 | AGGGAGGATGCTAGA[A/G]CCTGGCCCTGTTGTA | 1161 |
rs755460244 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935877 | CCATCCCTGCATTCC[G/T]GGTATGAAACCCACT | 1161 |
rs755468016 | snp | C/G | 6.59446e-05 | 0.00574177 | missense | ERCC8 | GRCh38.p7 | 5:60899663 | TTTTCCCATTATGTT[C/G]ATCAAGAGTAATCAA | 1161 |
rs755499319 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896571 | GTTCTATCTGATAGC[A/C]CTTTAAAAATCTGAA | 1161 |
rs755529763 | snp | A/G | 1.85249e-05 | 0.00304337 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945242 | CTGGCAGCGCTGGAA[A/G]CTGGGTGGACGGCAT | 1161 |
rs755615008 | snp | C/T | 6.59511e-05 | 0.00574206 | missense | ERCC8 | GRCh38.p7 | 5:60899692 | AAACATCCTGATGCT[C/T]TTCTCACATCCCATA | 1161 |
rs755631503 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901619 | AGTTAACTGTATTCA[C/T]GTCCACCTTTTCCTC | 1161 |
rs755656702 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944934 | AGGTTTTCTTTACCT[C/T]CGTGTTGACTCTGCT | 1161 |
rs755684940 | snp | A/C | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916570 | AAAGGTCATGACATT[A/C]ATTTAATTGTTAAAA | 1161 |
rs755712452 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889408 | TCTCCTGGACTCAAG[C/T]AATTCTCTTGCTTCA | 1161 |
rs755714557 | in-del | -/AGA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925843 | CTTTCTTTTTTTCTG[-/AGA]AGAAGTCTCGCTCTG | 1161 |
rs755721665 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902717 | GTATTTTATTGTAAA[A/G]GAACTGGTTTTGCTT | 1161 |
rs755736782 | snp | A/G | 1.6686e-05 | 0.00288838 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902395 | TAGACTTTTCAAAAT[A/G]CTTATTATTAATTAC | 1161 |
rs755836979 | snp | A/G | 1.65291e-05 | 0.00287476 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945350 | AATTCGGGAACAAAT[A/G]CTACTACATCCCGCA | 1161 |
rs755864063 | in-del | -/ATTT | 3.33372e-05 | 0.00408258 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922208 | TTTATTATTTAGTCC[-/ATTT]ATTTATGATTGCAAA | 1161 |
rs755876778 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894891 | AAATAGTGATTTGTC[A/G]GCTGGGCGTGGTCTC | 1161 |
rs755884189 | in-del | -/ATCT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886811 | ATTCCACTTTTAGGA[-/ATCT]ATCTAAAGACATAGT | 1161 |
rs755891113 | in-del | -/A | 1.65659e-05 | 0.00287796 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902424 | ACTAACTTCAAAAGC[-/A]AATAAGTTAAATTTT | 1161 |
rs755922328 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60880360 | TGGAGTTGCTCTTCT[C/T]GAGGAGTATCTTTGT | 1161 |
rs755933210 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881714 | ACCATTGGAAAAGTG[C/T]AGTATTAGGGTGGGA | 1161 |
rs755984039 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939215 | GTCTAAAAAAAATTT[C/T]GCAGCCATATTATAT | 1161 |
rs756058348 | snp | C/T | | | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903446 | GAGCTTCCCCAATGA[C/T]CATTGTTCATATAAA | 1161 |
rs756080352 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886563 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGTACCT | 1161 |
rs756100102 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893969 | TTGACCTGGTAATTG[A/C]TCCTGGGAATTTATC | 1161 |
rs756143581 | snp | A/G | | | intron-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60924362 | TGGTTGATTCCTAAG[A/G]AATGGCTAATGAGAA | 1161 |
rs756154024 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879827 | TTTATCCAATTTGCC[A/C]GTCTGTGTCTTTTAA | 1161 |
rs756192813 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920682 | ATATGTCCATTTTCA[A/G]ATTCAAAGTCACACT | 1161 |
rs756226436 | snp | A/T | 1.7065e-05 | 0.00292099 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945070 | GCTCAGGGGCGGGAC[A/T]GGAACAGCAGAGTCT | 1161 |
rs756252376 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936047 | TATTGGCTTCACAGG[A/C]GGATTTAGGGAGGAA | 1161 |
rs756281859 | snp | C/G | 1.91122e-05 | 0.00309124 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945226 | ACTGCGGGTCCCGCT[C/G]CTGGCAGCGCTGGAA | 1161 |
rs756331457 | in-del | -/CTATTTCTCAG | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944199 | CATGGCCTGTTGATT[-/CTATTTCTCAG]ACGTTGTTCAAATCT | 1161 |
rs756333058 | snp | A/C | 1.69758e-05 | 0.00291335 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903764 | ATCATAAGTCATCAT[A/C]AAAAGGAAACAAGAC | 1161 |
rs756351144 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908241 | TTTTTTGGTTTGGAA[G/T]GTTTGCATTATACTT | 1161 |
rs756373005 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881646 | GGCTCTGTGGGCGTC[A/G]GACCCTCCGAGCCAG | 1161 |
rs756396607 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939576 | CTCAGTTCACTGCAA[C/G]CTCCACCAAGAGATC | 1161 |
rs756486205 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943809 | GTGAAGGTGAACTTA[C/T]AGACATAAATGAGGA | 1161 |
rs756507627 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898044 | GCACTCCCATTGAGA[A/T]CAGTGGCTCAGTAGA | 1161 |
rs756579630 | snp | A/C | 1.65919e-05 | 0.00288022 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922059 | AAATACATACCTGCC[A/C]ATGGAACACACTGCT | 1161 |
rs756589300 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896258 | TTTTGCTCTTGTTGC[C/T]CAGGCTGGAGTGCAA | 1161 |
rs756644829 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923418 | ATATGATCTTATTAG[C/T]TTTTTTGGCATAAAA | 1161 |
rs756711431 | snp | A/G | 1.65157e-05 | 0.0028736 | missense | ERCC8 | GRCh38.p7 | 5:60898400 | TTATGAGCAGTGTTT[A/G]CTGCAATGAAAAACA | 1161 |
rs756728683 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937188 | GAGGCAGCAGGGGAG[C/T]GAAGTGGCCTCTATG | 1161 |
rs756728786 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60921577 | GAGTAAGTAGAGAGA[C/T]AAGACAGGGGTGAGT | 1161 |
rs756745528 | snp | C/T | 1.65652e-05 | 0.0028779 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928838 | ACTTAGAAAGAAAAA[C/T]GATTATACAAGTATA | 1161 |
rs756854640 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934474 | ATATTCTGGATATTA[A/G]TCCTCTGTTGGATGT | 1161 |
rs756861049 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913461 | TATCATTTTTTATTG[C/T]GTCTATTTGATTCTC | 1161 |
rs756880941 | in-del | -/A | 3.30196e-05 | 0.00406309 | frameshift-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928875 | TTACTATCTCCCTTC[-/A]ACAGGTTCAATGTCA | 1161 |
rs756937549 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896369 | CTACAGGTGCCCACC[A/G]CTGGCTAATTTTTTG | 1161 |
rs756997996 | snp | A/T | 1.64866e-05 | 0.00287106 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60899682 | AAGAGTAATCAAACA[A/T]CCTGATGCTCTTCTC | 1161 |
rs757002955 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927746 | AAGTGAGTGCCCCCC[A/C]AGCTGTCCTTGAATA | 1161 |
rs757085016 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941795 | CAGAGACAAGAAAAA[C/G]ATATAAGAAGGAAAT | 1161 |
rs757136010 | snp | C/T | | | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60903156 | AATATATAAATTATA[C/T]TCTATCTTTTCATTG | 1161 |
rs757163920 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926301 | ACACGTCTTTCTTCA[C/T]TGAGAATGTCTTGTT | 1161 |
rs757164182 | snp | A/T | 1.64798e-05 | 0.00287047 | missense | ERCC8 | GRCh38.p7 | 5:60887444 | ATAATATTTACCTCA[A/T]CATCATCAGGAACTG | 1161 |
rs757197052 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60887518 | GCTACCACTATAAAG[C/T]TCCTATAACATAGAA | 1161 |
rs757206580 | snp | A/C/G | 0.000100571 | 0.00709065 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903752 | TAAGATAATTTTATC[A/C/G]TAAGTCATCATCAAA | 1161 |
rs757241825 | in-del | -/CCT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881241 | TGTCTCAGAGGTGCA[-/CCT]GGCTCTGTGAGGTGT | 1161 |
rs757244374 | in-del | -/ATCA | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917857 | CCTTCAAGTTTTTAG[-/ATCA]ATCAAAGATAAATCC | 1161 |
rs757247559 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929231 | TAGCTGAGGACATCT[A/G]ATGGACAAAAGCATA | 1161 |
rs757251935 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940297 | GGCTATGGCTACGCA[C/T]AGTGGCCTGCAGAAG | 1161 |
rs757281101 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938727 | TACAAAAAGTATGTA[C/T]GTTCTCCACTTAAGG | 1161 |
rs757341351 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879496 | CCATTATTATTGTGT[-/G]GGAGTCTAAGTCTCT | 1161 |
rs757354905 | snp | C/T | 1.70229e-05 | 0.00291739 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898256 | ATTTATACCCAAATA[C/T]ATACTTAAAAATCTC | 1161 |
rs757361456 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908339 | CTCAGTACATAGTGA[C/G]GCACAAATCTGTATA | 1161 |
rs757443935 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937468 | TTGGGTGAGGCTTGC[C/T]GCTGCTGCTGTGGTA | 1161 |
rs757486843 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895934 | TGTCTTGTCCTTAGG[G/T]TTTCTTCCTCCAATC | 1161 |
rs757529880 | snp | A/C | 1.6768e-05 | 0.00289546 | missense | ERCC8 | GRCh38.p7 | 5:60874652 | CTCCAGGCATCTTCA[A/C]AGGCCGGATTTAATT | 1161 |
rs757535592 | snp | C/G | 4.9525e-05 | 0.00497595 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945030 | TCCTCACACCGGCTG[C/G]AGCACTGGACGTCGC | 1161 |
rs757556931 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60916096 | ATGTCTTCTGCTTCA[C/T]TTCTTAAGTCTATGG | 1161 |
rs757559414 | snp | C/T | 4.95708e-05 | 0.00497825 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899750 | GAAATAAATGTTACA[C/T]TGACATATGTAGCTA | 1161 |
rs757566299 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914789 | AGACTCTTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 1161 |
rs757568990 | snp | C/T | 3.3123e-05 | 0.00406945 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945404 | TGGCGGCGTGGGCAG[C/T]GATTGCGTGGTCAGT | 1161 |
rs757590900 | snp | C/G | 1.69605e-05 | 0.00291204 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945064 | GACAGAGCTCAGGGG[C/G]GGGACTGGAACAGCA | 1161 |
rs757608738 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931574 | TTCACCTCCCAAAGT[A/G]CTGGGATTACAGGTG | 1161 |
rs757671582 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900923 | AACCTTCATACCTCT[C/T]CAGCTAGCCTTCTTA | 1161 |
rs757695476 | snp | C/T | 1.65649e-05 | 0.00287788 | missense, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918347 | TCATGAGGATACCAC[C/T]GTACAGTCTCCACAC | 1161 |
rs757741277 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888393 | CTAACTGTGGCTGAT[G/T]CAAAGATATATATGT | 1161 |
rs757761341 | snp | C/G | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919966 | TGATGAGCATTCAAA[C/G]TCCTATTTAGAGGAA | 1161 |
rs757826905 | snp | C/T | 1.66402e-05 | 0.00288441 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922054 | ATTTTAAATACATAC[C/T]TGCCAATGGAACACA | 1161 |
rs757842428 | in-del | -/TTA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899547 | TTTGTCAATATGCGT[-/TTA]TTATGTGGCTTCAAT | 1161 |
rs757855977 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911282 | TGACTTTTTAATAAT[A/C]GCCATCCTAACTGGT | 1161 |
rs757859353 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892943 | ACCAAGGCAGCAATA[C/G]TTCCCCAGAACCCTC | 1161 |
rs757873744 | in-del | -/T | 1.90842e-05 | 0.00308897 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945227 | TGCGGGTCCCGCTGC[-/T]TGGCAGCGCTGGAAA | 1161 |
rs757909289 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908883 | GTATGTTTTGTGAAA[C/T]ACCTTTGACCTCTTA | 1161 |
rs757975394 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937774 | CACAGTGCCTGCAGC[A/G]GCAATCCACTTCCTT | 1161 |
rs758094991 | snp | C/T | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919709 | CTGATATAGGATAAA[C/T]TAAACTAGTGGAAAA | 1161 |
rs758109819 | snp | A/G | 1.65302e-05 | 0.00287486 | synonymous-codon, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922083 | CACTGCTTTACATGT[A/G]TAATAAGATTGTCTG | 1161 |
rs758132869 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914973 | TTTTTGTATGTTGCT[A/G]GATTCTACATATTAA | 1161 |
rs758162984 | snp | A/G | 1.66291e-05 | 0.00288345 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928816 | AAAGCAGGTTTTACT[A/G]CATTTCACTTAGAAA | 1161 |
rs758220986 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929226 | AAATGTAGCTGAGGA[C/T]ATCTAATGGACAAAA | 1161 |
rs758230027 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905270 | CTAGAATTGCCCCTT[C/T]TTTGAAATCATACAT | 1161 |
rs758255760 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891689 | TCCTGCTGATACTTC[C/T]TTTATTTCTGTTGTA | 1161 |
rs758296965 | snp | A/C | 1.6504e-05 | 0.00287258 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902518 | TGTGACCTGCAAATA[A/C]AACTATATGAAAAGT | 1161 |
rs758299849 | snp | A/T | 1.64879e-05 | 0.00287118 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945018 | CAGCATATCGTGTCC[A/T]CACACCGGCTGGAGC | 1161 |
rs758307373 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914073 | GTATATTCTGTTGAT[G/T]TGGGGTGGAGAGTTC | 1161 |
rs758331383 | snp | C/T | 2.07682e-05 | 0.00322237 | intron-variant, missense | ERCC8 | GRCh38.p7 | 5:60903600 | AACGTTTCTTTTTAT[C/T]GAATCGTTTACTCAA | 1161 |
rs758506477 | snp | C/G | 1.65721e-05 | 0.0028785 | missense | ERCC8 | GRCh38.p7 | 5:60890937 | AGTTTTATAATGTCC[C/G]TTAAGCATAGTTATC | 1161 |
rs758580431 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906030 | CTGGTGTCAGACATG[-/A]AAAAAATCCTGAAAA | 1161 |
rs758583502 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896462 | TGATCCACCCACCTC[C/T]GCCTCCCAAAGTGCT | 1161 |
rs758595033 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944963 | CTCTCCGAAGGCGAA[A/G]AGGGTCCTCCAAACC | 1161 |
rs758627045 | snp | A/T | 4.94833e-05 | 0.00497385 | missense | ERCC8 | GRCh38.p7 | 5:60899715 | ATCCCATAATTTTAC[A/T]CTACTGTCAGCACTG | 1161 |
rs758627730 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888651 | TATCTGTGATAGATG[A/G]AGGAGTTCATTTGGG | 1161 |
rs758675665 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883614 | TTTCAAATTTCTGAC[A/T]GGTAATTAGTGGCAA | 1161 |
rs758784351 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934618 | TTTGCTTTTCGGTTC[C/T]TGGTCATGAAGTCTT | 1161 |
rs758815354 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889663 | CAATTTGGTAGAAAG[A/C]AATAATTTGTGGTTA | 1161 |
rs758846868 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932794 | CCCCAACACAATGGC[A/T]TAGGAGTAGAGGGAA | 1161 |
rs758855828 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931311 | ATTAAATTTTTTTTT[-/A]AAATTTACTTTTAGA | 1161 |
rs758866798 | in-del | -/GAAG | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942623 | TTAGTAGTTTCTAGA[-/GAAG]GAAGAGGGTAAAGCA | 1161 |
rs758873406 | snp | C/T | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873794 | AAGGGAAAATTAAGA[C/T]TACCTTCATGATAAT | 1161 |
rs758941200 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911013 | TTTGTATCAAATTAA[A/G]GAATTTCTCTTCTAT | 1161 |
rs759043794 | snp | C/T | 2.03689e-05 | 0.00319124 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945209 | GCTGGAGCATTACCC[C/T]TACTGCGGGTCCCGC | 1161 |
rs759054651 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897992 | CTTTAATTTATATCA[A/G]TAGTCCTCAGTCTTT | 1161 |
rs759093720 | snp | C/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945905 | CCTTTTCGGTGGCAC[C/T]CTGGCTCCGGCGCTG | 1161 |
rs759120854 | snp | A/G/T | 4.89995e-05 | 0.00494952 | intron-variant, missense | ERCC8 | GRCh38.p7 | 5:60903588 | TACACTGTTAGTAAC[A/G/T]TTTCTTTTTATTGAA | 1161 |
rs759164753 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923063 | GTGGAAGGGAAAGAG[C/T]GGTGAGAGATGAGAG | 1161 |
rs759192025 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924255 | CAATTTATACATTTA[C/T]ATAAAGTGTTGCTAT | 1161 |
rs759195176 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883109 | CAGTTGAAAACTCAA[C/T]AGAAAAGCAAAATTA | 1161 |
rs759234910 | in-del | -/AAAAAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886703 | GAGACTCCATCTCAA[-/AAAAAT]AAAAATAAAAATAAA | 1161 |
rs759251563 | snp | A/T | 1.656e-05 | 0.00287745 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874725 | GGAAGATTCTGTTTT[A/T]TCTACTTCATAATTT | 1161 |
rs759345078 | snp | A/G | 2.22933e-05 | 0.00333859 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891128 | TCATCTCTGAAATCT[A/G]AATTTAAAACACAAC | 1161 |
rs759415447 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918100 | CATACAGCTGTCAGC[A/G]GCACAGCCAGGATAT | 1161 |
rs759439267 | snp | A/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945831 | TGACCCAGAGCTGAG[A/T]GGTGTAATTGAAGAG | 1161 |
rs759503277 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932377 | CTGTGCCTAAACTAT[C/T]TGAGAAAATAATGTG | 1161 |
rs759620638 | in-del | -/T | 1.6636e-05 | 0.00288405 | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918408 | AAACAGCAATCAAAA[-/T]TTTACATTAACTGAC | 1161 |
rs759630974 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942835 | ATGTTTTTTTAGAGG[A/G]TGTAAACTGTGAACA | 1161 |
rs759710901 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885112 | TGAACTCTTGGGCTC[A/G]GTGATCCTCCCACCT | 1161 |
rs759739190 | snp | G/T | 3.29794e-05 | 0.00406061 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887529 | AAAGTTCCTATAACA[G/T]AGAAGGCAAAGATGA | 1161 |
rs759867306 | snp | A/G | 4.96931e-05 | 0.00498439 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918310 | AGTTTTATCAAATGA[A/G]CTTGATGTGAACATG | 1161 |
rs759925501 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876128 | GTGAGAACTTGGCGG[C/T]GTTTGGGTTTTTGTC | 1161 |
rs759954468 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904153 | TAATAGCTTAGTTTT[A/T]CCAAGTTAATGATAT | 1161 |
rs760004770 | in-del | -/TGTAAGATAGCTACCTTTTTGAATTTTTTTTTTTTTTTTTTTT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938328 | TCAAAGAATGTGGCC[lengthTooLong]TTGAGACGGAGTCTC | 1161 |
rs760018315 | snp | C/T | 3.30453e-05 | 0.00406467 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944894 | CATTGGTCCAGATTC[C/T]AACTGGCCTGTTAGC | 1161 |
rs760042081 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892225 | ATAACCAGTGAGATC[G/T]CCAATCTTATATACA | 1161 |
rs760069012 | in-del | -/AAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930137 | TACATATAGTACAAC[-/AAT]GACAAGCAGGCCAGG | 1161 |
rs760088589 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893886 | GTGCAACTCTCATCA[C/T]TATCCATCTCTAGAA | 1161 |
rs760097652 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914647 | GTTAAAAAATTAGCC[A/G]GAGATGGTGGTGCAC | 1161 |
rs760097765 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930385 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 1161 |
rs760125962 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913286 | CCTGTTATTGGTCTA[C/T]TCAGAGATTCAACTT | 1161 |
rs760158488 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889253 | ATATTTTGTAGGGTG[A/G]TATGTTGAGATTATA | 1161 |
rs760176314 | snp | A/G | 6.60851e-05 | 0.00574789 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899747 | GAAGAAATAAATGTT[A/G]CATTGACATATGTAG | 1161 |
rs760183166 | in-del | -/TTTTA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933138 | TACCTTTTATTTTTG[-/TTTTA]ATGTTTTAAATGGCT | 1161 |
rs760189458 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884136 | GTCCCAGATCATAAG[C/T]AGAATAAATGGCAGA | 1161 |
rs760203200 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60922221 | CCATTTATTTATGAT[C/T]GCAAATTTCTAAAAA | 1161 |
rs760239968 | snp | A/G | 2.12042e-05 | 0.00325602 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891115 | ATAATAAGGTTACTC[A/G]TCTCTGAAATCTGAA | 1161 |
rs760263364 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945008 | ACAAAAACCCCAGCA[C/T]ATCGTGTCCTCACAC | 1161 |
rs760327827 | snp | A/G | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919252 | CTTCAACATAATTAT[A/G]AGGGTGGATGGGTGG | 1161 |
rs760376969 | snp | A/C | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916538 | GGCTACAAGATATTC[A/C]ATTATAGTCAGAAGT | 1161 |
rs760388795 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904461 | AAATTGGGAAAGTTG[C/T]CAAATTTTATTCATG | 1161 |
rs760389824 | snp | A/G | 1.64928e-05 | 0.00287161 | missense | ERCC8 | GRCh38.p7 | 5:60902475 | TAGTCATAACGTGGA[A/G]ACCAGGAAACTGCTA | 1161 |
rs760463251 | snp | C/T | 4.97187e-05 | 0.00498567 | synonymous-codon, missense, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918286 | TGTATTTGTATCCCA[C/T]ACTTTCAGAGTTTTA | 1161 |
rs760464394 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925660 | ATCTTTTAGTTGTCA[A/G]TGGTTTGTTCCCACT | 1161 |
rs760535564 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920563 | AAATAGTCTAAGTCA[C/T]ATTAACTTAATAATA | 1161 |
rs760543594 | snp | A/C | 3.36072e-05 | 0.00409908 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904904 | CATTTAAAAAGTATA[A/C]GGTTTAAGTATAAAA | 1161 |
rs760625492 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935238 | GTTTTGTCTTGTAGA[G/T]GTCTTTTACCTCCCT | 1161 |
rs760643141 | in-del | -/TA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927301 | GTGTTTTGAACAAGT[-/TA]TATATACACATCGAT | 1161 |
rs760649059 | snp | A/T | 3.29734e-05 | 0.00406025 | missense | ERCC8 | GRCh38.p7 | 5:60899645 | ATTCAACAGCTTGTG[A/T]CTTTTTCCCATTATG | 1161 |
rs760695589 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895421 | CTCATTTTGGTGGAC[C/T]TGGGTTTTAAACACT | 1161 |
rs760761028 | snp | A/G | 1.65288e-05 | 0.00287474 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60890988 | ATAAACAGCAATGGT[A/G]CTACCATATGGTACA | 1161 |
rs760766050 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901980 | TTTTGACTATATGCC[C/T]CATTAGATCATTAGA | 1161 |
rs760774979 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889382 | CAGTGGTGTGAACAC[A/G]GCTCACTCAATCTCC | 1161 |
rs760813961 | snp | A/G | 1.67038e-05 | 0.00288992 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928979 | AAAATAAAAGGGGGA[A/G]AAAGAAATTAACAAG | 1161 |
rs760829217 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60887878 | TTCAATAAAGACTTC[A/G]GTGAAGAAACCATAT | 1161 |
rs760858795 | snp | C/G | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944062 | AAGTACAACTTGCTT[C/G]TTCCCTTTGGAAAAC | 1161 |
rs760871685 | in-del | -/TGGTTGAA | | | intron-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60924326 | TCTCTCTTGTCATTC[-/TGGTTGAA]TGATTTCATTCTCTG | 1161 |
rs760977099 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926726 | TGAGTTACATGTATA[C/T]TACAACCAATTCCCA | 1161 |
rs760999419 | snp | A/C | 1.69169e-05 | 0.00290829 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945309 | ATCGCTGTCAAGGGA[A/C]GTGAAGGAGCACGTG | 1161 |
rs761007820 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929025 | AAATTTCTTATTTAA[A/C]CAAGATTACTTATGG | 1161 |
rs761070076 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938350 | TAGCTACCTTTTTGA[-/A]TTTTTTTTTTTTTTT | 1161 |
rs761106797 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883152 | ATTATTTTTGTATGG[-/T]TAAGCAAAGAAACAA | 1161 |
rs761125490 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939652 | ACCGCACCCGGAGCA[C/T]GCCCGGCTGATTTTT | 1161 |
rs761127625 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924599 | ATTTATCCTAGAAAA[A/G]CTTTCTTGAATTATT | 1161 |
rs761146190 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927662 | GAGTAACAGTATTGA[C/T]TACTTTCCTGACCAG | 1161 |
rs761175984 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60916017 | CCCCCTTCTACTTAG[C/T]AAGTACTGCACTGCA | 1161 |
rs761219261 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938699 | AACAATTTTGGTAAA[G/T]GTACCACTGACTTAC | 1161 |
rs761238198 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917573 | TAAAGGCAAGGTAAA[C/T]AGAAAAGAGAGGTAT | 1161 |
rs761259907 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906160 | CAATCATTTATGTCT[A/C]TTTATTTATTTATTT | 1161 |
rs761318132 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935361 | TTGGTGTATAGCAGA[C/G]CTACTGACTTGTGTA | 1161 |
rs761386858 | snp | G/T | 1.65836e-05 | 0.0028795 | missense, stop-gained, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918272 | GTACTTACTTGTAAT[G/T]TATTTGTATCCCATA | 1161 |
rs761437354 | snp | A/G | 1.64991e-05 | 0.00287215 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944907 | TCTAACTGGCCTGTT[A/G]GCCAAAAAGTAAGGT | 1161 |
rs761626209 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894368 | TTTAGAATGGGGTAA[A/T]AACTGAGAATAGGTA | 1161 |
rs761713754 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885713 | AAAAGGTATTTTTTT[A/C]TCTTTATTTGGATTA | 1161 |
rs761734310 | snp | C/T | 6.04382e-05 | 0.00549686 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945220 | ACCCCTACTGCGGGT[C/T]CCGCTGCTGGCAGCG | 1161 |
rs761787794 | snp | C/T | 0.000188235 | 0.0096996 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945296 | GCGCCTTGTGGAGAT[C/T]GCTGTCAAGGGAAGT | 1161 |
rs761898657 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890677 | AGAAACAGAATTTAT[A/G]CCAATCAAGTTGCAC | 1161 |
rs761909479 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917726 | TAGAAAAGTAGAGAC[A/T]TATCAGAGTAGAGCT | 1161 |
rs761922710 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910317 | AGTCTTGATATCTGA[C/T]AGTGAAGTCTTCCAA | 1161 |
rs761959654 | snp | C/G | 3.30142e-05 | 0.00406276 | missense | ERCC8 | GRCh38.p7 | 5:60898382 | AAGCCATTAACTTTC[C/G]CATTATGAGCAGTGT | 1161 |
rs762029625 | snp | A/C | 6.60327e-05 | 0.00574561 | synonymous-codon, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928875 | TTACTATCTCCCTTC[A/C]ACAGGTTCAATGTCA | 1161 |
rs762045064 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907689 | TAACCTCTGTCCCCA[C/T]TGGCTCATTCCCAAC | 1161 |
rs762072406 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875853 | AGACGCCTGCCACCA[C/T]GCCTGGATAATTTTT | 1161 |
rs762091425 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883035 | TAAGCCACATGAGGG[C/T]CATGCTTCCTAATCC | 1161 |
rs762095842 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926978 | ATTAACTATGAGATA[A/C]TTTTTGCTGATAGAG | 1161 |
rs762100082 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936090 | TTTTGGAACAGTGTC[A/C]ATAGGATTGATACAA | 1161 |
rs762131478 | in-del | -/G | 1.64917e-05 | 0.00287151 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887423 | GTCACTGTACCATTT[-/G]TGAAAATAATATTTA | 1161 |
rs762154192 | snp | C/T | 3.30038e-05 | 0.00406212 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899618 | ATTTATTAATGCGTT[C/T]TTCCTTACCTGATTC | 1161 |
rs762155125 | in-del | -/CTTTT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923883 | CATCATCACTCTTTC[-/CTTTT]CACCTCAAAGTAACT | 1161 |
rs762182568 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926895 | TGTTTTGACTCTGTT[A/G]AAATGGCTTCCAAAA | 1161 |
rs762184037 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932263 | AACATAGCAGGCCTG[A/C]GACGGCTACCCTTAA | 1161 |
rs762206204 | snp | A/C/T | 9.89654e-05 | 0.00703383 | missense | ERCC8 | GRCh38.p7 | 5:60902494 | AGGAAACTGCTAATA[A/C/T]TTCTTGTCTGTGACC | 1161 |
rs762230648 | snp | G/T | 1.64792e-05 | 0.00287042 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60887473 | TGGTTCATATAAGGA[G/T]GGAACCCAAGCCAGA | 1161 |
rs762324516 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941636 | CACATCATAATTAAA[C/T]TGCTGAAAACTAAAG | 1161 |
rs762331965 | snp | C/T | 2.35336e-05 | 0.00343019 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874717 | AAGAAAAAGGAAGAT[C/T]CTGTTTTTTCTACTT | 1161 |
rs762370366 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925821 | CTGCATTGACATTGT[C/T]ATCTTTCTTTCTTTT | 1161 |
rs762372457 | snp | A/G | 5.39884e-05 | 0.00519531 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945473 | CTAGTCAACTAACGC[A/G]TCATGCGACACTTAG | 1161 |
rs762392333 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894570 | AATTCTTTGCTTGTA[C/G]TCCAAAGGTGTAGTG | 1161 |
rs762433995 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939677 | ATTTTTGGATTTTTA[A/G]TAGAGATGGGGTTTT | 1161 |
rs762439504 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882553 | GCGCATGCCACCGGC[A/G]AATTTTTGTATTTTT | 1161 |
rs762475445 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908960 | CGTATCTATATGTAG[A/G]CTCTAATATGACTTT | 1161 |
rs762493229 | in-del | -/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945999 | GCTGATTCCTTTCTC[-/G]GGAGTTGACATTCCA | 1161 |
rs762499617 | snp | C/T | 1.66604e-05 | 0.00288616 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903732 | CTGTAAAAACAGAAC[C/T]GGTTTAAGATAATTT | 1161 |
rs762521037 | snp | A/C | 1.71123e-05 | 0.00292504 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890855 | TCTGGCAAGCTAGCT[A/C]GCTGAACATTTTAAA | 1161 |
rs762561563 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935741 | TGCTGAGGGTTTTAA[C/T]CATAATGGGATGCTG | 1161 |
rs762592885 | in-del | -/TTT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938086 | ATATATATATATATA[-/TTT]TATTTTTTTTTTTTT | 1161 |
rs762621931 | snp | A/G | 1.64803e-05 | 0.00287052 | missense | ERCC8 | GRCh38.p7 | 5:60887496 | AAGCCAGAATGTTGC[A/G]GTCTCTGCTACCACT | 1161 |
rs762640246 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895552 | TCGTGAAAAAGCAAA[C/T]GAAATAATCCATATG | 1161 |
rs762699661 | snp | A/G | | | missense | ERCC8 | GRCh38.p7 | 5:60898325 | CTCATTCGATTATCT[A/G]TACCAACAGTGAGGA | 1161 |
rs762701301 | snp | A/C/G/T | 3.30116e-05 | 0.00406262 | missense, synonymous-codon | ERCC8 | GRCh38.p7 | 5:60898378 | ACATAAGCCATTAAC[A/C/G/T]TTCCCATTATGAGCA | 1161 |
rs762844822 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931217 | TATTAAATGCATCTC[C/T]TGATTATAAGATTAA | 1161 |
rs762850414 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912993 | GTTGGATTCAGTCTG[A/C]CAGTATTTTATTGAG | 1161 |
rs762857331 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886223 | CTTGATGTGAAAGTT[A/G]AAAAAAAATACAGAG | 1161 |
rs762859018 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900209 | TGAATAATGAGGACA[A/G]TGCATTTCCATTTGG | 1161 |
rs762922071 | snp | A/G | 1.66893e-05 | 0.00288867 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945052 | GGACGTCGCCATGAC[A/G]GAGCTCAGGGGCGGG | 1161 |
rs762932374 | snp | A/C | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944324 | CCTAACTTGGCTCCC[A/C]CTCTTGTTCTCAGTT | 1161 |
rs762942785 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924147 | CTGGACTTTGGTGAC[G/T]GCATTCATGTGCTAT | 1161 |
rs762950598 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60887370 | TTAAAAGTCTCTCTC[A/C]CATAAAGTAACAAAA | 1161 |
rs762956399 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895172 | GAGACTCTACCTCAA[-/A]AAAAAAAAAAAAAAA | 1161 |
rs763048023 | snp | A/C/G | 6.09878e-05 | 0.00552185 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945212 | GGAGCATTACCCCTA[A/C/G]TGCGGGTCCCGCTGC | 1161 |
rs763091752 | snp | A/C | 1.74351e-05 | 0.0029525 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922020 | ATACTCAACTATTTA[A/C]AAATTCATAAATTTT | 1161 |
rs763099457 | snp | G/T | 8.77982e-05 | 0.00662506 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874710 | AAAGATAAAGAAAAA[G/T]GAAGATTCTGTTTTT | 1161 |
rs763179626 | snp | C/G | | | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919453 | ATTCCTTAAGATGAA[C/G]GTTTGGGACCTTAAA | 1161 |
rs763193486 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933287 | GCTGTGGTGCAATCT[C/T]GGCTCACTGCAACCT | 1161 |
rs763247709 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897643 | GAATATAGCACCTTC[A/G]AAATATATTTATTGC | 1161 |
rs763252721 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904028 | TTTCCCCAACGATTA[C/T]GTGTGAGGTAACTAA | 1161 |
rs763252894 | snp | C/T | 1.65594e-05 | 0.0028774 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899769 | CATATGTAGCTAGGA[C/T]AATGACTGTACCCCT | 1161 |
rs763257985 | in-del | -/AAGTATAAGGTTT | 3.33751e-05 | 0.0040849 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904897 | CAAAAGACATTTAAA[-/AAGTATAAGGTTT]AAGTATAAAAACAAA | 1161 |
rs763277105 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881416 | ATTTAAGTCTGCAGA[C/G]GTTTCTGCTGCCTTT | 1161 |
rs763400295 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944995 | GTTTGGCGTGCGGAC[A/G]AAAACCCCAGCATAT | 1161 |
rs763429701 | snp | C/T | 3.53688e-05 | 0.00420513 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903557 | AAAGTACATTAGTCA[C/T]GTCACTTACAAAGAA | 1161 |
rs763453717 | snp | C/T | 8.24722e-05 | 0.006421 | missense | ERCC8 | GRCh38.p7 | 5:60902469 | AAGATATAGTCATAA[C/T]GTGGAGACCAGGAAA | 1161 |
rs763483902 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913663 | TTGCTCTTGCTTCTC[C/T]AGTTCTTTTAATTGG | 1161 |
rs763490257 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905765 | AGAGTTTAACTGATG[A/C]AAGGCTGGCCAGGCC | 1161 |
rs763544234 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884166 | AACTGGGATTCAAAC[C/G]CAGTTTCCTGAAGCT | 1161 |
rs763569872 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927304 | GTTTTGAACAAGTTA[C/T]ATACACATCGATTTT | 1161 |
rs763582111 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892349 | TCATCAGATTCTCCA[A/G]TGGCCAAGCATTCCA | 1161 |
rs763598004 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939533 | GACAGAGTCTCGCTC[G/T]GTCACCCAGGCTGGA | 1161 |
rs763633337 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934306 | GGTAATATCACATTG[C/T]GGTTTTGATTTGCAC | 1161 |
rs763648993 | snp | C/T | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873564 | AGCCTGTAATCCCAG[C/T]TACTCAGGAGGCTTA | 1161 |
rs763696210 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898625 | GAAAAAATTTCTGCC[C/T]AACATACTTTTCTTT | 1161 |
rs763742189 | snp | C/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945996 | CTCGCTGATTCCTTT[C/T]TCGGGAGTTGACATT | 1161 |
rs763765479 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911493 | ACTCTGGATATTAGC[C/T]CTTTGTCAGATGGGT | 1161 |
rs763784608 | snp | A/T | 3.37206e-05 | 0.00410599 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890870 | AGCTGAACATTTTAA[A/T]TTCCTGTATCACTCT | 1161 |
rs763847634 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891173 | ATACTTAAAATATTA[C/T]GCTATAAAAAGGGCT | 1161 |
rs763851415 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905955 | GGGGAATGGTCCTCT[C/T]GTGCACTAAGCCACT | 1161 |
rs763870903 | in-del | -/AGAA | 1.66101e-05 | 0.0028818 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928827 | TACTGCATTTCACTT[-/AGAA]AGAAAAATGATTATA | 1161 |
rs763872466 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920649 | GTTATTATAACTCAT[G/T]TTGTAAAGATGCATA | 1161 |
rs763918354 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895873 | CCCAAATATGAACTG[G/T]AAAGTGTTGAATGAG | 1161 |
rs764033667 | snp | A/G | 1.68678e-05 | 0.00290407 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945060 | CCATGACAGAGCTCA[A/G]GGGCGGGACTGGAAC | 1161 |
rs764057678 | snp | A/G | 1.99774e-05 | 0.00316043 | intron-variant, missense | ERCC8 | GRCh38.p7 | 5:60903603 | GTTTCTTTTTATTGA[A/G]TCGTTTACTCAAAGT | 1161 |
rs764096335 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897396 | TAAGCTCCATGAGGA[C/T]AGGACTTTTCCATGT | 1161 |
rs764116898 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60887941 | AAGTTTTATTTAACT[C/T]ACAGCTGCCTAACTG | 1161 |
rs764120654 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902051 | GCACAATGCTTGGCA[C/T]GTGGGAGGAAGTCAT | 1161 |
rs764169694 | snp | A/T | 1.72543e-05 | 0.00293715 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922029 | TATTTACAAATTCAT[A/T]AATTTTTACATTTTA | 1161 |
rs764191406 | snp | A/T | 1.76999e-05 | 0.00297483 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945467 | GAGCCCCTAGTCAAC[A/T]AACGCATCATGCGAC | 1161 |
rs764193963 | snp | A/G | 3.32309e-05 | 0.00407607 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922153 | GAACCACCTGATAAC[A/G]TGCTGATAATAAAAA | 1161 |
rs764210552 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889425 | ATTCTCTTGCTTCAG[C/T]CTCCTGCACAGCTGG | 1161 |
rs764233629 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937342 | GGGTTAGGTGGTGGG[A/C]AGGCCGATAGAGCTC | 1161 |
rs764274194 | snp | A/C | 1.71246e-05 | 0.00292609 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898249 | TTTCTTAATTTATAC[A/C]CAAATATATACTTAA | 1161 |
rs764310097 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60916085 | CTGTTCTTCAAATGT[C/T]TTCTGCTTCATTTCT | 1161 |
rs764314054 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902711 | CATATGGTATTTTAT[C/T]GTAAAAGAACTGGTT | 1161 |
rs764406810 | snp | A/C | 0.00011532 | 0.00759255 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944999 | GGCGTGCGGACAAAA[A/C]CCCCAGCATATCGTG | 1161 |
rs764468873 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930683 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 1161 |
rs764483506 | snp | A/G | 3.33667e-05 | 0.00408439 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902393 | TGTAGACTTTTCAAA[A/G]TGCTTATTATTAATT | 1161 |
rs764483984 | snp | C/T | 4.96282e-05 | 0.00498113 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945395 | GAGGTGAGGTGGCGG[C/T]GTGGGCAGCGATTGC | 1161 |
rs764534023 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925713 | GGGATACTTCATGAC[C/T]TAGTTTGGTTGTAAG | 1161 |
rs764612686 | snp | C/G | 0.00136339 | 0.0260737 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945049 | ACTGGACGTCGCCAT[C/G]ACAGAGCTCAGGGGC | 1161 |
rs764773120 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906290 | ATCCACCCTCCTTGG[C/T]TTCCCAAAGTGTTGG | 1161 |
rs764795272 | snp | A/G | | | intron-variant, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919448 | TTTGGATTCCTTAAG[A/G]TGAAGGTTTGGGACC | 1161 |
rs764797215 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935390 | TATGTTAATTTTGTA[A/T]CCTGAAACTTCGCTG | 1161 |
rs764804312 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894429 | TGATTTATATAAATC[A/G]TAATTATGAAAATTA | 1161 |
rs764862119 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892780 | GCAGCCGGATGAACT[C/T]GTCCAGGTAGACCTC | 1161 |
rs764902694 | snp | C/T | 1.65247e-05 | 0.00287438 | missense | ERCC8 | GRCh38.p7 | 5:60890993 | CAGCAATGGTGCTAC[C/T]ATATGGTACAAAAAC | 1161 |
rs764937712 | snp | C/T | 1.6569e-05 | 0.00287824 | missense | ERCC8 | GRCh38.p7 | 5:60903707 | TGTACTTTGGGTCCT[C/T]TAGTACCAACTGTAA | 1161 |
rs764967895 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883488 | AATTCTACTGACAGA[C/T]AGTGTCAATGTTATA | 1161 |
rs764975568 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60880063 | TAGGGCAGGCCTGGT[-/G]GTGACAAAATCTCTC | 1161 |
rs764991231 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905621 | CTTTCAGGACCAACT[-/A]CTCATCTCTGTCACT | 1161 |
rs765096023 | snp | A/C | 2.34299e-05 | 0.00342263 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891135 | TGAAATCTGAATTTA[A/C]AACACAACAAAGCCT | 1161 |
rs765096428 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944153 | ATTATTCATTCTTCT[C/T]TTTTTGTCATTCACG | 1161 |
rs765217473 | in-del | -/TTTA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939007 | GAAACAGCTTTTAGC[-/TTTA]TTTGTTTTAAAAATT | 1161 |
rs765252344 | snp | A/G | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873662 | GGCCTGAGCGACAGA[A/G]TGAAACTCCATCTCA | 1161 |
rs765358514 | snp | A/G | 1.65351e-05 | 0.00287528 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945390 | CTGGAGAGGTGAGGT[A/G]GCGGCGTGGGCAGCG | 1161 |
rs765406204 | in-del | -/C | 1.64787e-05 | 0.00287038 | frameshift-variant | ERCC8 | GRCh38.p7 | 5:60887457 | CATCATCATCAGGAA[-/C]TGGTTCATATAAGGA | 1161 |
rs765418087 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938728 | ACAAAAAGTATGTAC[A/G]TTCTCCACTTAAGGG | 1161 |
rs765442561 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60928254 | CTGAAAGGAGTAAAA[C/G]TATATGTAATACTGC | 1161 |
rs765480995 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912401 | TCTGTTTGTCTGTTA[C/T]TGGTATATAGGAATG | 1161 |
rs765525249 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917808 | CTATTATCCATTGCT[C/T]GTCTTTACTAAGCTA | 1161 |
rs765529545 | snp | A/G | 3.30316e-05 | 0.00406383 | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944899 | GTCCAGATTCTAACT[A/G]GCCTGTTAGCCAAAA | 1161 |
rs765571269 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896400 | TATTTTTAGTAGAGA[C/T]GGGGTTTCATCGTGT | 1161 |
rs765682382 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913412 | TCTCTGATGGTAGTT[C/T]GTATTTCTGTGGGAT | 1161 |
rs765685293 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925877 | AGCCCAGACTGGAGT[A/G]CAGTGGCATGATCTC | 1161 |
rs765693087 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902590 | ATTTTGCCTGATTCT[A/G]AAGAAAGTGAGGCCA | 1161 |
rs765693910 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938335 | ATGTGGCCTGTAAGA[C/T]AGCTACCTTTTTGAA | 1161 |
rs765708773 | snp | C/T | 1.6486e-05 | 0.00287102 | missense | ERCC8 | GRCh38.p7 | 5:60899665 | TTCCCATTATGTTGA[C/T]CAAGAGTAATCAAAC | 1161 |
rs765709309 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927014 | AGAGATATGGTTTCA[C/T]GTTTTTATATAGACA | 1161 |
rs765771011 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904687 | ATATATATATATAAA[A/G]TTGTGATATTCCTCT | 1161 |
rs765812673 | snp | A/G | 9.88435e-05 | 0.00702937 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944938 | TTTCTTTACCTCCGT[A/G]TTGACTCTGCTCTCC | 1161 |
rs765839209 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909089 | TGATAATTTTTGGAA[A/C]GTTTTGGCTTTAAAA | 1161 |
rs765876964 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894659 | CCACCCCAATCCTAC[C/T]GAAAATAATCTTCAT | 1161 |
rs765931804 | snp | A/T | 3.29538e-05 | 0.00405904 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945009 | CAAAAACCCCAGCAT[A/T]TCGTGTCCTCACACC | 1161 |
rs765944681 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882023 | GTTTTTTGTATTTTT[A/C]GTAGAGACGGGGTTT | 1161 |
rs765986851 | snp | C/T | 1.64925e-05 | 0.00287158 | stop-gained | ERCC8 | GRCh38.p7 | 5:60902478 | TCATAACGTGGAGAC[C/T]AGGAAACTGCTAATA | 1161 |
rs766040320 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60921137 | AAGAACCACAGGGCA[C/T]GTATACTGATTTCTA | 1161 |
rs766049153 | snp | C/G | 1.68032e-05 | 0.0028985 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904905 | ATTTAAAAAGTATAA[C/G]GTTTAAGTATAAAAA | 1161 |
rs766160147 | snp | A/T | 1.65225e-05 | 0.00287419 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945371 | ACATCCCGCAGTACA[A/T]GAACTGGAGAGGTGA | 1161 |
rs766191028 | snp | G/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917233 | TTGGCTCAATGTAAT[G/T]GTAAAAAAAGATGTG | 1161 |
rs766209592 | snp | A/G | 1.65707e-05 | 0.00287838 | missense, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918296 | TCCCATACTTTCAGA[A/G]TTTTATCAAATGAGC | 1161 |
rs766229856 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886390 | GTAAACTGGTAAAAT[C/T]TGACGTGAGAACAAA | 1161 |
rs766254137 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932297 | GTTCTGCTTGCAAGA[C/T]TGGCTCTTGGTTACA | 1161 |
rs766319396 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876060 | CAGGTCCCGGTGTGT[A/G]ATGTTCCCCTTCCTG | 1161 |
rs766320443 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907610 | GTCAATCCCCCTACT[C/T]GTGTTCAGATTCCCT | 1161 |
rs766328589 | in-del | -/GCAAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906144 | CCGGAATAATGGCTG[-/GCAAT]CATTTATGTCTCTTT | 1161 |
rs766343468 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927381 | GCTATCAAAAGGGGT[C/T]AATGCAAAATACAAG | 1161 |
rs766412691 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924589 | TCCAGATCTTATTTA[C/T]CCTAGAAAAGCTTTC | 1161 |
rs766516991 | snp | C/T | 0.000115394 | 0.00759499 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60899661 | CTTTTTCCCATTATG[C/T]TGATCAAGAGTAATC | 1161 |
rs766544842 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925972 | GGGATTACGGGCACG[C/T]GCCACTGCACCTGGC | 1161 |
rs766565870 | in-del | -/C | 3.30666e-05 | 0.00406598 | frameshift-variant | ERCC8 | GRCh38.p7 | 5:60890978 | AGTAAACTGTATAAA[-/C]AGCAATGGTGCTACC | 1161 |
rs766570070 | snp | A/G | 1.65072e-05 | 0.00287286 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899730 | TCTACTGTCAGCACT[A/G]AGAAGAAATAAATGT | 1161 |
rs766601270 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940016 | CTTTTGCAATTCTTT[G/T]TCTTTATTACTATTT | 1161 |
rs766601928 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877561 | TTCCTTGAGCAGTGG[C/T]TTGTAGATCTCCTTG | 1161 |
rs766619032 | in-del | -/TG | 1.64814e-05 | 0.00287061 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904908 | AAAAAGTATAAGGTT[-/TG]TAAGTATAAAAACAA | 1161 |
rs766625482 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897734 | TATAAGTCATATATA[A/G]TACAGGTTAAGTATC | 1161 |
rs766671945 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910914 | GTTGAACAGAGGAAA[C/T]AATGAGGATAATGCA | 1161 |
rs766733295 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935747 | GGGTTTTAATCATAA[C/T]GGGATGCTGGATTTT | 1161 |
rs766753800 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881664 | CCCTCCGAGCCAGGC[A/G]CAGGATATAATCTCC | 1161 |
rs766788043 | snp | A/G | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873653 | CTGCACTCCGGCCTG[A/G]GCGACAGAGTGAAAC | 1161 |
rs766796146 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892386 | CTTCATTGACTTGCT[C/T]GGTATCCTCGATGTC | 1161 |
rs766805422 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898937 | TATATAGTTTACATG[C/T]TTCATAAGGTTTTTT | 1161 |
rs766816262 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904218 | GGACACAGACTGAAA[C/G]GACCTCAAGACAACT | 1161 |
rs766822890 | snp | A/C | 3.31373e-05 | 0.00407032 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60890940 | TTTATAATGTCCCTT[A/C]AGCATAGTTATCTGT | 1161 |
rs766910186 | snp | A/C | 1.82901e-05 | 0.00302402 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922186 | TTCACATTAATTTAT[A/C]ATTTTATTTATTATT | 1161 |
rs766959543 | snp | C/T | 1.64991e-05 | 0.00287215 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928906 | AGGGTGTTAATTCCA[C/T]CGCCGTGGATTCTTT | 1161 |
rs766970981 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896280 | GGAGTGCAATGGCGC[A/G]ATCTCGGCTCACCGC | 1161 |
rs766973173 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882195 | AGAATGTTCATTTTC[A/C]TTTTGATGAATATGA | 1161 |
rs766988940 | in-del | -/AAA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895170 | GCGAGACTCTACCTC[-/AAA]AAAAAAAAAAAAAAA | 1161 |
rs767017619 | in-del | -/TTTGGTGACTCTA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913574 | ATTTTTTGAAGGGTT[-/TTTGGTGACTCTA]CTTCCTTCAGTTCTA | 1161 |
rs767021259 | snp | A/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945834 | CCCAGAGCTGAGTGG[A/T]GTAATTGAAGAGGAG | 1161 |
rs767082671 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60916277 | TTTATGAAATTGACT[A/G]AAGTCCCACTCATTT | 1161 |
rs767092500 | snp | C/T | 1.66493e-05 | 0.0028852 | missense | ERCC8 | GRCh38.p7 | 5:60890890 | TGTATCACTCTTACC[C/T]GGAAATTTGACTGAA | 1161 |
rs767147543 | snp | C/T | 1.65395e-05 | 0.00287567 | missense | ERCC8 | GRCh38.p7 | 5:60890972 | CTCCTGAGTAAACTG[C/T]ATAAACAGCAATGGT | 1161 |
rs767246930 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900156 | TGGTATGATTTGGTG[-/T]TTTTTTCCTTTTTAT | 1161 |
rs767285347 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934236 | TTTTCACCATATCCA[C/T]GCCAACATCTACTAT | 1161 |
rs767296496 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902700 | GGTATTTCAAACATA[C/T]GGTATTTTATTGTAA | 1161 |
rs767317479 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907935 | AATATGTTCCTCATC[C/T]GATTTAATCTGTCAG | 1161 |
rs767341656 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942068 | AAAAGTAAGTATTTT[A/G]TAATTCCTAGAGCAG | 1161 |
rs767351074 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891952 | CCAACACTGCCATCA[A/G]CATTGCCAGAGAGGT | 1161 |
rs767402803 | snp | A/G | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919031 | AGTGACCAACATAGT[A/G]TGTTACCTAACTGGA | 1161 |
rs767407764 | snp | C/T | 3.41378e-05 | 0.00413131 | upstream-variant-2KB, synonymous-codon | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945298 | GCCTTGTGGAGATCG[C/T]TGTCAAGGGAAGTGA | 1161 |
rs767453650 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895648 | ATAACATTCCCTCAT[C/T]TGTGTCTTCTGATCC | 1161 |
rs767461322 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899516 | AATGCCTTTTGAAAA[A/T]TCATAAAGTTTGCAA | 1161 |
rs767492717 | snp | A/C | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918182 | CATATATGACATCTC[A/C]GCAAATAATCATACT | 1161 |
rs767509925 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60932509 | TTGAGTCTCTAATGA[A/G]CTTCCCTGATAGACA | 1161 |
rs767533851 | snp | C/T | 3.30262e-05 | 0.0040635 | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904866 | TCAAAATTAAATACA[C/T]CTGCAGTCTGGTAAT | 1161 |
rs767595500 | snp | A/T | 3.43395e-05 | 0.0041435 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922176 | AATAAAAAAGTTCAC[A/T]TTAATTTATCATTTT | 1161 |
rs767630736 | snp | C/T | 1.64909e-05 | 0.00287144 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60899631 | TTCTTCCTTACCTGA[C/T]TCAACAGCTTGTGAC | 1161 |
rs767650815 | snp | A/C | 1.65067e-05 | 0.00287282 | missense | ERCC8 | GRCh38.p7 | 5:60898384 | GCCATTAACTTTCCC[A/C]TTATGAGCAGTGTTT | 1161 |
rs767676286 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878868 | tgtgtctctatttcc[C/T]tcagttctgctctga | 1161 |
rs767725923 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881628 | TGTGCTAGCAATGGG[A/C]GAGGCTCTGTGGGCG | 1161 |
rs767779011 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907882 | CAATCTTATTTTTAT[C/G]GCACTACTGTAAATC | 1161 |
rs767786136 | snp | C/T | 0.000165498 | 0.00909515 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874718 | AGAAAAAGGAAGATT[C/T]TGTTTTTTCTACTTC | 1161 |
rs767821376 | snp | C/T | 2.6582e-05 | 0.00364558 | intron-variant, missense | ERCC8 | GRCh38.p7 | 5:60903584 | AGAATACACTGTTAG[C/T]AACGTTTCTTTTTAT | 1161 |
rs767849136 | in-del | -/ATTACAACC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879679 | TTATCAGAGACTAGG[-/ATTACAACC]ATTACAACCTCTGCC | 1161 |
rs767882137 | snp | C/T | 1.67826e-05 | 0.00289673 | missense | ERCC8 | GRCh38.p7 | 5:60874656 | AGGCATCTTCAAAGG[C/T]CGGATTTAATTGTGA | 1161 |
rs767891039 | snp | G/T | 3.32331e-05 | 0.0040762 | synonymous-codon, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922056 | TTTAAATACATACCT[G/T]CCAATGGAACACACT | 1161 |
rs767898409 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923217 | CCTACAAAATTATTC[C/T]ATTCAAAAACTTTGC | 1161 |
rs767903180 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881210 | TGTTGCTAGCTGATC[A/G]TTCCTCTGGGAGTTT | 1161 |
rs767970249 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876141 | GGTGTTTGGGTTTTT[G/T]TCCTTGCAATAGTTT | 1161 |
rs768003199 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898840 | GTAGTCTCAAAATTT[A/G]TATCACTTACAAAAT | 1161 |
rs768059470 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937155 | TCTCAGCCGTGGATA[C/T]CAGCACCGGCAACCG | 1161 |
rs768093230 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885642 | ATAAACCAAATTAGA[C/T]GTGATAAAATCTGGA | 1161 |
rs768178214 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882768 | CAGTTGTATACTGAA[A/G]TCTGTTCATTTTGTC | 1161 |
rs768225604 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875360 | CATAGGTTTCCCTCA[C/G]GGATTTGTCTGAAGG | 1161 |
rs768229773 | snp | A/G | 1.65021e-05 | 0.00287241 | synonymous-codon, intron-variant | ERCC8 | GRCh38.p7 | 5:60904859 | TGTTTCCTCAAAATT[A/G]AATACATCTGCAGTC | 1161 |
rs768280897 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909962 | CGAGACTCCGTCTAG[-/A]AAAAAAAAAAAATAA | 1161 |
rs768281582 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60874709 | AAAAGATAAAGAAAA[A/C]GGAAGATTCTGTTTT | 1161 |
rs768343436 | in-del | -/TGT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929852 | TCTTAATCTGTTGGC[-/TGT]TATTAGCATCTACAC | 1161 |
rs768360763 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894418 | ATTAACTTTATGATT[-/A]TATATAAATCATAAT | 1161 |
rs768366104 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913324 | GTTTAGTCTTGGGAG[A/G]GTGTGTGTGTCGAGG | 1161 |
rs768382250 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891907 | ACTGGTGCTTGGATC[A/G]GAAGGGAAGTGAGAT | 1161 |
rs768383125 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942269 | CAGTTTCTTAAAAAG[A/T]AAAGGATTTATCTAG | 1161 |
rs768423381 | snp | C/T | 6.63658e-05 | 0.00576008 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918262 | ATGTTTTAATGTACT[C/T]ACTTGTAATGTATTT | 1161 |
rs768456073 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926936 | GATTCCATTAACTTT[C/G]TATTTGAAGTATCTG | 1161 |
rs768474789 | snp | A/T | 3.31906e-05 | 0.0040736 | missense, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918386 | TGAACATCAGGATGA[A/T]CTCTACAAAACAGCA | 1161 |
rs768508952 | in-del | -/AA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895171 | CGAGACTCTACCTCA[-/AA]AAAAAAAAAAAAAAA | 1161 |
rs768573249 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936264 | GTTGCGTATTTCCAG[G/T]AATTTATTCATCTCC | 1161 |
rs768765553 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933150 | TTGTTTTAATGTTTT[A/C]AATGGCTTTTATAGG | 1161 |
rs768857559 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911132 | TTGTTACATAGGTAT[A/G]TATGTGCCATGTTGG | 1161 |
rs768862791 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890488 | TCCCTTTACTAGCCA[C/T]TGGTAGAAAATAAGG | 1161 |
rs768863053 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905460 | CAACTGCCAATATCT[G/T]CAATTCCTTTGCTAA | 1161 |
rs768881018 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935861 | ACTTGCATATGTTAA[A/G]CCATCCCTGCATTCC | 1161 |
rs768882550 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940615 | CCTGAGTGAGGCATG[A/C]ATAGATCTAACCCTG | 1161 |
rs768903965 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891138 | AATCTGAATTTAAAA[C/G]ACAACAAAGCCTAGG | 1161 |
rs768929845 | snp | G/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946453 | GCCTTTTTCTGTAAC[G/T]TATTTTAATATTTAG | 1161 |
rs769008937 | in-del | -/A | 1.64857e-05 | 0.00287099 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904765 | AGTTTTCAGTATGTC[-/A]AAAGACAAAAGAATA | 1161 |
rs769022895 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884108 | TTCTGATATTTGGAA[A/T]TATTATAAGCTTGTC | 1161 |
rs769026318 | snp | A/G | 1.65655e-05 | 0.00287793 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945041 | GCTGGAGCACTGGAC[A/G]TCGCCATGACAGAGC | 1161 |
rs769122789 | in-del | -/AAAG | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60874701 | AAAAAAAAAAAAGAT[-/AAAG]AAAAAGGAAGATTCT | 1161 |
rs769203284 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929468 | GCTGGGCATGGTGGT[A/G]GGCTCCTATGCAGGA | 1161 |
rs769245412 | snp | A/G | 2.19812e-05 | 0.00331513 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874711 | AAGATAAAGAAAAAG[A/G]AAGATTCTGTTTTTT | 1161 |
rs769273326 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882875 | AGTTTATTAAAAGAC[A/G]TCTTGTCATTGGGGG | 1161 |
rs769275330 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909816 | AAAATTAGCCAGGCA[C/T]GGTGACACACGCCTG | 1161 |
rs769301124 | in-del | -/A | 0.0501759 | 0.150234 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874686 | ATTTTGTTGTAGTCT[-/A]AAAAAAAAAAAGATA | 1161 |
rs769310773 | in-del | -/ATACATACATATATATATATATATATAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938041 | TACATACATACATAC[-/ATACATACATATATATATATATATATAT]ATATATATATATATA | 1161 |
rs769323668 | snp | C/T | 0.000244251 | 0.0110483 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945280 | TCTCAGGATTTGTTC[C/T]GCGCCTTGTGGAGAT | 1161 |
rs769360018 | snp | C/T | 2.03328e-05 | 0.00318842 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945210 | CTGGAGCATTACCCC[C/T]ACTGCGGGTCCCGCT | 1161 |
rs769378958 | snp | C/T | 1.64942e-05 | 0.00287173 | synonymous-codon, intron-variant | ERCC8 | GRCh38.p7 | 5:60904850 | ACTATAAACTGTTTC[C/T]TCAAAATTAAATACA | 1161 |
rs769380455 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888857 | GTAACCAACAAAATC[A/T]TATTATTACCACCAT | 1161 |
rs769486837 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926417 | AGTCACAAATAGTTC[A/G]TGAACTAGTAGCATG | 1161 |
rs769518632 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915406 | AATTCAAACATAAAG[C/G]TTGTCTGCTATTGTA | 1161 |
rs769521761 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929883 | ACTAATTTAACCAGA[A/T]TTATTTCTAAATTCA | 1161 |
rs769599998 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943137 | TTAGCTAGGTGTGTG[A/G]GCACATGTCTGTGGT | 1161 |
rs769608740 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914306 | ATATTTAGGATAGGT[A/G]GCTCTTCTTGTTGTG | 1161 |
rs769618520 | snp | A/C/T | 3.30122e-05 | 0.00406266 | missense, synonymous-codon | ERCC8 | GRCh38.p7 | 5:60898366 | ATCACTTGTAAAACA[A/C/T]AAGCCATTAACTTTC | 1161 |
rs769632784 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918089 | TTGCCCAATGTCATA[-/C]AGCTGTCAGCAGCAC | 1161 |
rs769636207 | in-del | -/AT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938045 | TACATACATACATAC[-/AT]ACATATATATATATA | 1161 |
rs769702207 | snp | A/G | 1.65293e-05 | 0.00287479 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928854 | GATTATACAAGTATA[A/G]TAAACTTACTATCTC | 1161 |
rs769714861 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60877402 | TTTAGTTTTTTCCAA[-/T]TCTGTGAAGAAAGTC | 1161 |
rs769715995 | snp | A/T | 1.65351e-05 | 0.00287528 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945034 | CACACCGGCTGGAGC[A/T]CTGGACGTCGCCATG | 1161 |
rs769752797 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937870 | TCACGATATGCATCT[C/T]CATACACTGCTCTGT | 1161 |
rs769754405 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60922560 | GCTCTGGGCAAGTTA[G/T]ACCACCTGTCTAAGA | 1161 |
rs769763390 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898952 | TTTCATAAGGTTTTT[C/T]AAAAAACTATATAAA | 1161 |
rs769809365 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906987 | TTTACAAAAAAAGGC[C/G]ATGAGCCAGACTTGC | 1161 |
rs769814126 | in-del | -/ATT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938350 | TAGCTACCTTTTTGA[-/ATT]TTTTTTTTTTTTTTT | 1161 |
rs769846329 | snp | A/C | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918905 | TCACATCTTATGTAA[A/C]CCACCATCCATAAAA | 1161 |
rs769853030 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900168 | GTGTTTTTTTCCTTT[C/T]TATATAAAAAACGGT | 1161 |
rs769899051 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60887272 | TGCCCAGGCTGGTCT[G/T]GATTTCTGGGCTCAA | 1161 |
rs769901024 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893587 | CATCATCATGATCAG[C/T]TTGAAAGCAGATAGG | 1161 |
rs769923160 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890720 | ATTCATTCATACATT[A/G]TATGCTGTCTAACAA | 1161 |
rs770002373 | snp | A/G | 3.6025e-05 | 0.00424396 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903553 | GCACAAAGTACATTA[A/G]TCATGTCACTTACAA | 1161 |
rs770019628 | in-del | -/AAAGAA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60874701 | AAAAAAAAAAAAGAT[-/AAAGAA]AAAGGAAGATTCTGT | 1161 |
rs770068024 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907203 | AAATATACCAACTCA[G/T]TCACAACAGGTAATT | 1161 |
rs770094427 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883864 | GCCAGATTCCTCAAA[A/G]TATAATAAAACAGTC | 1161 |
rs770117039 | in-del | -/GCGTGGGCAGCGATT | 1.65399e-05 | 0.0028757 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945393 | AGAGGTGAGGTGGCG[-/GCGTGGGCAGCGATT]GCGTGGGCAGCGATT | 1161 |
rs770120973 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901434 | ATCCTATGGGCCCTT[-/A]AATCAGCTCCCTCAC | 1161 |
rs770131914 | in-del | -/A/AA | 0.000166782 | 0.00913059 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904893 | AATCAAAAGACATTT[-/A/AA]AAAAAGTATAAGGTT | 1161 |
rs770132141 | snp | A/C/G | 6.39779e-05 | 0.00565558 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874704 | AAAAAAAAAGATAAA[A/C/G]AAAAAGGAAGATTCT | 1161 |
rs770144236 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883055 | CTTCCTAATCCTACT[A/G]TGGAAGCCCAGTGTG | 1161 |
rs770215298 | snp | A/G | 1.91364e-05 | 0.00309319 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891093 | ATAGTTCACCTGTAG[A/G]ATTAAAATAATAAGG | 1161 |
rs770326126 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944989 | AAACCCGTTTGGCGT[A/G]CGGACAAAAACCCCA | 1161 |
rs770369595 | in-del | -/AAA | 0.000260298 | 0.0114053 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874686 | ATTTTGTTGTAGTCT[-/AAA]AAAAAAAAAGATAAA | 1161 |
rs770382966 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933096 | ATGGCACATGCTTGC[C/T]CAAATTTCCTATTTA | 1161 |
rs770410662 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924166 | TTCATGTGCTATAAT[G/T]TAAAATAATTTCTAT | 1161 |
rs770467685 | snp | A/G | 1.65021e-05 | 0.00287241 | missense | ERCC8 | GRCh38.p7 | 5:60902451 | TTTTACCTTGCTGTT[A/G]CCAAGATATAGTCAT | 1161 |
rs770470142 | in-del | -/CCT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908365 | TATATTCAGTGTAGA[-/CCT]CCTCACTCCTGAATT | 1161 |
rs770494554 | in-del | -/CAAAGTAGTTGC | 1.81145e-05 | 0.00300947 | intron-variant, cds-indel | ERCC8 | GRCh38.p7 | 5:60903613 | ATTGAATCGTTTACT[-/CAAAGTAGTTGC]CGTTTGAAATAAAAT | 1161 |
rs770499406 | snp | C/T | 1.65067e-05 | 0.00287282 | missense | ERCC8 | GRCh38.p7 | 5:60898350 | TGAGGAGGTGAAGTC[C/T]ATCACTTGTAAAACA | 1161 |
rs770508120 | snp | G/T | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873401 | AACAACTGGCTGGGT[G/T]CAGTGGCTCAAGCTT | 1161 |
rs770572117 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896223 | CTCATATTAATATTT[A/C]TTTTTTGTTTGAGAC | 1161 |
rs770585176 | snp | A/C/T | 1.6897e-05 | 0.00290658 | missense | ERCC8 | GRCh38.p7 | 5:60874671 | CCGGATTTAATTGTG[A/C/T]TTTTGTTGTAGTCTA | 1161 |
rs770587198 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60900350 | GCAAATCTATGATCA[A/G]ACATCTATTTCAGCT | 1161 |
rs770659328 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917343 | GTTGCAGCAAAGCAT[C/T]TGTGTTGAAAACTGG | 1161 |
rs770666820 | snp | A/C | 5.75357e-05 | 0.00536326 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874689 | TTGTTGTAGTCTAAA[A/C]AAAAAAAAGATAAAG | 1161 |
rs770769052 | snp | G/T | 0.000183847 | 0.0095859 | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918434 | CTGACTTATGTGAGT[G/T]TCAAAACTGGTACTA | 1161 |
rs770806254 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901676 | CATGTGCCAAACTAG[C/G]TGTACCCTCCACCCT | 1161 |
rs770810014 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925329 | GTTTCTATTGTCTCT[G/T]TACTGCTCAATTTGG | 1161 |
rs770827004 | snp | A/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946991 | GCTCAGTAGTATTCC[A/G]TTGTATGGGTTTGCC | 1161 |
rs770858013 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899823 | CACACAGAGGTCTCG[G/T]TATATAGGTACATAT | 1161 |
rs770926234 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884937 | AATTTCTCATATACA[A/G]AAGTTTGTTTACACG | 1161 |
rs770949190 | snp | C/G | 1.65214e-05 | 0.0028741 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922094 | ATGTGTAATAAGATT[C/G]TCTGCTGGAGTTCTC | 1161 |
rs771033574 | snp | G/T | 2.12809e-05 | 0.0032619 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891116 | TAATAAGGTTACTCA[G/T]CTCTGAAATCTGAAT | 1161 |
rs771035497 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895527 | CATCATTTACTTATA[C/G]AGTTATGTATCGTGA | 1161 |
rs771052829 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912367 | CAATTGAGAATGTAG[A/T]TTACTCATGATTTGG | 1161 |
rs771084942 | snp | A/G | 5.01567e-05 | 0.00500758 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928980 | AAATAAAAGGGGGAG[A/G]AAGAAATTAACAAGT | 1161 |
rs771093989 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936151 | CTGTGAGTCTGTACC[C/T]AAACTTTTTTTGGTA | 1161 |
rs771226360 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885535 | AAATGTAAAATAAAT[A/G]GCTAAACCTAATTAT | 1161 |
rs771262517 | snp | A/C/T | 3.30585e-05 | 0.00406551 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902436 | AGCAAATAAGTTAAA[A/C/T]TTTACCTTGCTGTTG | 1161 |
rs771310171 | snp | A/G | 1.72803e-05 | 0.00293936 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890838 | CTTTTACATATAACT[A/G]GTCTGGCAAGCTAGC | 1161 |
rs771313714 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920264 | CTTCCAATAAATTTC[A/G]CTTAAGATAAGCAGA | 1161 |
rs771315801 | snp | C/T | 1.65239e-05 | 0.00287431 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902545 | AAGTCTTGCAAGATA[C/T]CTGAAAAATCAGAAG | 1161 |
rs771352926 | in-del | -/ATACATAC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938025 | TGTGTGTGTGTGTGT[-/ATACATAC]ATACATACATACATA | 1161 |
rs771360980 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930050 | CAAGTAATTATAAGC[A/G]TTTTGGAAATCATTT | 1161 |
rs771365290 | snp | C/G/T | 3.3105e-05 | 0.00406837 | missense | ERCC8 | GRCh38.p7 | 5:60890960 | TAGTTATCTGTTCTC[C/G/T]TGAGTAAACTGTATA | 1161 |
rs771439902 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929146 | CAGCAGTAGTAACAA[-/T]TTACATGCAAACTTT | 1161 |
rs771470240 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926641 | CTCTAATTGTGTACA[C/T]AGAGAAATATTTGTA | 1161 |
rs771477075 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905777 | ATGCAAGGCTGGCCA[C/G]GCCAAGTGCGAGATG | 1161 |
rs771618734 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897224 | GTGAAGCCTACCCTG[A/C]CTTCCCTATGTGAAA | 1161 |
rs771661150 | snp | A/G | 1.65787e-05 | 0.00287907 | missense, synonymous-codon, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918278 | ACTTGTAATGTATTT[A/G]TATCCCATACTTTCA | 1161 |
rs771715120 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889150 | AGAAGTGATGTCCCA[C/T]AACTGGGATGCTAAC | 1161 |
rs771740295 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878453 | AAGGAATGGTACCAG[C/T]TCCTCCTTGTACCTC | 1161 |
rs771787946 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940466 | GCAGAACAGGGTAAC[A/T]GAACCCTAAAGTTTC | 1161 |
rs771793120 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902423 | TACTAACTTCAAAAG[C/T]AAATAAGTTAAATTT | 1161 |
rs771845197 | snp | A/G | 0.00024626 | 0.0110937 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891111 | TAAAATAATAAGGTT[A/G]CTCATCTCTGAAATC | 1161 |
rs771877637 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939643 | GCACCTGCCACCGCA[C/T]CCGGAGCACGCCCGG | 1161 |
rs771929603 | snp | A/G | | | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874590 | AAAAGTTTCAGCAGA[A/G]ACAAAAAGGTACTAA | 1161 |
rs771940512 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890272 | GTTTCATTTTCCTTA[C/T]CTACAAAACAGGGAA | 1161 |
rs771948491 | snp | C/G | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919153 | TGTGTATTTAAGATA[C/G]TGGTACTGTAGTTAT | 1161 |
rs772119030 | snp | A/G | | | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874466 | GTTTTAGGATTTTAT[A/G]CAAATATTAACCTCA | 1161 |
rs772173555 | snp | C/T | 0.000137931 | 0.0083034 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945449 | TAAAGGAGGGAAAAG[C/T]GAGAGCCCCTAGTCA | 1161 |
rs772187289 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901814 | CCCAGCAGATAAATA[C/T]GCAATACTCTTTTTC | 1161 |
rs772296837 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910564 | TCTCAATAATGTTCT[A/G]AAGTTCTCTGTGTAT | 1161 |
rs772429684 | snp | A/C | 1.6543e-05 | 0.00287597 | missense | ERCC8 | GRCh38.p7 | 5:60903680 | CAGGATCCAGACTTC[A/C]AGTCACAAAGTTGTA | 1161 |
rs772489808 | snp | C/G | 1.76939e-05 | 0.00297433 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945268 | GGCATGGGTTGGTCT[C/G]AGGATTTGTTCCGCG | 1161 |
rs772511071 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917435 | GTTTAGACAATGGGA[A/G]TCCCTAGAGGGTTTG | 1161 |
rs772524237 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907455 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGTGTCA | 1161 |
rs772598844 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931974 | CAACAGCTTGGGCTC[C/T]GATTTCTGTCTCCTC | 1161 |
rs772612104 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894275 | AGGCGTGAGCCACTG[C/T]GCCCGGCTGGGAATT | 1161 |
rs772618308 | in-del | -/AGA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940541 | TCCAGGAGATCACAG[-/AGA]AGAAGGAGCTCAGGA | 1161 |
rs772703915 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895329 | CTTACTTTCCCTTTA[C/G]GCTAACTTGTGCCAG | 1161 |
rs772742689 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911891 | AGGTTTGTCAAAGAT[C/T]GGATGGTTGTAGATG | 1161 |
rs772748790 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915451 | TTTTCTACTGATGCA[A/G]TAAGGAAAGTACTTA | 1161 |
rs772774972 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895531 | ATTTACTTATAGAGT[C/T]ATGTATCGTGAAAAA | 1161 |
rs772776073 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907602 | TTTTTAATGTCAATC[C/T]CCCTACTTGTGTTCA | 1161 |
rs772779979 | snp | A/G | 1.65378e-05 | 0.00287552 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60890973 | TCCTGAGTAAACTGT[A/G]TAAACAGCAATGGTG | 1161 |
rs772858650 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945000 | GCGTGCGGACAAAAA[C/T]CCCAGCATATCGTGT | 1161 |
rs772879291 | snp | A/G | 1.69841e-05 | 0.00291407 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945304 | TGGAGATCGCTGTCA[A/G]GGGAAGTGAAGGAGC | 1161 |
rs772886268 | snp | A/C | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946702 | CCCTTTATGGTGTAC[A/C]GTTTTATTGTTTTTG | 1161 |
rs772915192 | snp | C/T | 4.12516e-05 | 0.00454137 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891112 | AAAATAATAAGGTTA[C/T]TCATCTCTGAAATCT | 1161 |
rs772970902 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895102 | TTGAACCTGGGAGGT[A/G]GAGGCTGCAGTGAGC | 1161 |
rs773080678 | snp | C/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945563 | ATCGGAGCCCTACCC[C/G]GCCCGGCTCTGGGCG | 1161 |
rs773110100 | snp | G/T | 3.30447e-05 | 0.00406464 | upstream-variant-2KB, synonymous-codon | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945363 | ATACTACTACATCCC[G/T]CAGTACAAGAACTGG | 1161 |
rs773128630 | snp | C/G | 1.75409e-05 | 0.00296145 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874592 | AAGTTTCAGCAGAGA[C/G]AAAAAGGTACTAAAG | 1161 |
rs773129964 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898960 | GGTTTTTTAAAAAAC[G/T]ATATAAATTCTAATA | 1161 |
rs773135356 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924099 | TAATTTATTTGTTGC[A/C]AAAACCAGATCATTT | 1161 |
rs773142538 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911957 | TAGGTCTATATCTCT[C/G]TTTTGGTACCAGTAC | 1161 |
rs773148897 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892302 | GGAGCAACTTGATCT[C/T]CATTTTGAGTGGGTC | 1161 |
rs773174804 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944288 | CAACTCTCTCCCGGA[C/T]AAGTGTAATCACAAC | 1161 |
rs773354540 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875990 | GTGTGCTGCACCCAT[G/T]TAACATTAGGTATAT | 1161 |
rs773382523 | snp | A/C | 4.94621e-05 | 0.00497279 | missense | ERCC8 | GRCh38.p7 | 5:60899639 | TACCTGATTCAACAG[A/C]TTGTGACTTTTTCCC | 1161 |
rs773402310 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882787 | GTTCATTTTGTCTTT[C/T]ATCCAAATGTTTACT | 1161 |
rs773463658 | snp | A/G | 1.66801e-05 | 0.00288787 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928977 | TAAAAATAAAAGGGG[A/G]AGAAAGAAATTAACA | 1161 |
rs773493249 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938499 | GCTGGGATTACAGGC[A/G]TGTGCCACCACACCC | 1161 |
rs773548683 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929921 | TTAAAATAATGCTAG[C/T]TTAAATATCAAATTA | 1161 |
rs773583014 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914540 | TCATGCTTGTAATCC[C/T]AACACTTTCAGAGGC | 1161 |
rs773586713 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927266 | TTTACAGCTCTCATG[A/G]TGGATGGTAAATATT | 1161 |
rs773624589 | snp | A/G | 1.64789e-05 | 0.0028704 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60887491 | AACCCAAGCCAGAAT[A/G]TTGCAGTCTCTGCTA | 1161 |
rs773636209 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60879242 | GAAAGACCGTTTGCT[-/A]ATAATTTCTGTTCTT | 1161 |
rs773657899 | in-del | -/ATTATT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883138 | TATACTTCATCATAA[-/ATTATT]TTTGTATGGTAAGCA | 1161 |
rs773679744 | snp | A/C | 6.60873e-05 | 0.00574798 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887559 | ATACTGTGGATCAAG[A/C]GCTGATATCAAACTG | 1161 |
rs773692532 | in-del | -/GGTCAGTGATTGCGA | 1.65869e-05 | 0.00287979 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945413 | GGGCAGCGATTGCGT[-/GGTCAGTGATTGCGA]GGTCAGTAAAGGAGG | 1161 |
rs773715726 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60903850 | TATGCCAAAATTACA[C/T]TGTCATTTTTAATGT | 1161 |
rs773778782 | snp | A/C/G | 5.03464e-05 | 0.00501708 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890876 | ACATTTTAAATTCCT[A/C/G]TATCACTCTTACCTG | 1161 |
rs773778831 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924233 | ACAAACCAATATCTA[A/G]ATCCATCAATTTATA | 1161 |
rs773803670 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890823 | AAATCATAATTTATT[A/C]TTTTACATATAACTG | 1161 |
rs773905349 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883062 | ATCCTACTATGGAAG[C/T]CCAGTGTGTAACCTA | 1161 |
rs773988847 | snp | C/T | 8.26358e-05 | 0.00642737 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945355 | GGGAACAAATACTAC[C/T]ACATCCCGCAGTACA | 1161 |
rs774047625 | snp | C/T | 1.6588e-05 | 0.00287988 | splice-donor-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918264 | GTTTTAATGTACTTA[C/T]TTGTAATGTATTTGT | 1161 |
rs774054490 | snp | C/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60947006 | ATTGTATGGGTTTGC[C/T]AGTTTATCTGTTCAC | 1161 |
rs774077463 | snp | A/T | 1.65042e-05 | 0.0028726 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899616 | ATATTTATTAATGCG[A/T]TCTTCCTTACCTGAT | 1161 |
rs774113866 | snp | A/G | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919041 | ATAGTGTGTTACCTA[A/G]CTGGATCTTGATTCA | 1161 |
rs774200185 | snp | A/T | 8.24708e-05 | 0.00642095 | missense | ERCC8 | GRCh38.p7 | 5:60899713 | ACATCCCATAATTTT[A/T]CTCTACTGTCAGCAC | 1161 |
rs774236171 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933865 | TTCACTTACAATATG[A/G]TCTCCAATTCCACCC | 1161 |
rs774315679 | in-del | -/GTA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926358 | GGTGTGTGTAATGAT[-/GTA]GTAGATTTATGTTTT | 1161 |
rs774357820 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943906 | AAGGAACTCTCAGAG[A/G]TATTTCACAACATTG | 1161 |
rs774429942 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon | ERCC8 | GRCh38.p7 | 5:60887470 | AACTGGTTCATATAA[A/G]GATGGAACCCAAGCC | 1161 |
rs774438381 | snp | C/T | 1.71176e-05 | 0.00292549 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945295 | CGCGCCTTGTGGAGA[C/T]CGCTGTCAAGGGAAG | 1161 |
rs774450945 | snp | A/G | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873403 | CAACTGGCTGGGTGC[A/G]GTGGCTCAAGCTTAT | 1161 |
rs774472045 | snp | C/T | 1.65113e-05 | 0.00287322 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928870 | TAAACTTACTATCTC[C/T]CTTCAACAGGTTCAA | 1161 |
rs774542633 | in-del | -/TGTAA | 1.65877e-05 | 0.00287986 | frameshift-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918266 | TTTAATGTACTTACT[-/TGTAA]TGTATTTGTATCCCA | 1161 |
rs774573184 | in-del | -/AAAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906735 | CTCTGTCTCAAAAAT[-/AAAT]AAATAAATAAATAAA | 1161 |
rs774679469 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935898 | GAAACCCACTTGATC[A/G]TGGTGGATTATATTT | 1161 |
rs774686181 | snp | A/C/G | 3.31635e-05 | 0.00407196 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945043 | TGGAGCACTGGACGT[A/C/G]GCCATGACAGAGCTC | 1161 |
rs774689949 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60922772 | CTCTGCTAAAACAAC[-/T]GTCAACAAGGCAGGC | 1161 |
rs774720177 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914611 | CCTGGGCAAGACAGA[C/G]AGACACTGCCTCTAC | 1161 |
rs774750637 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893811 | ATACACATAATATAA[A/G]ATTTACCATCATAAC | 1161 |
rs774768467 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923739 | ATATTATAAAATCTT[A/G]GACATTGTGAATGTT | 1161 |
rs774775163 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939889 | CCATTAGAAGCTTTT[-/A]AATAATATTTTCTTC | 1161 |
rs774831816 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60915651 | CTTCCAGAGACCACC[C/T]ACATTTCTTGGCTTG | 1161 |
rs774844813 | snp | A/C | 2.03159e-05 | 0.00318709 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945211 | TGGAGCATTACCCCT[A/C]CTGCGGGTCCCGCTG | 1161 |
rs774860429 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892387 | TTCATTGACTTGCTC[A/G]GTATCCTCGATGTCA | 1161 |
rs774899829 | snp | C/T | 1.6569e-05 | 0.00287824 | missense | ERCC8 | GRCh38.p7 | 5:60903708 | GTACTTTGGGTCCTC[C/T]AGTACCAACTGTAAA | 1161 |
rs774944497 | snp | A/G | 1.65545e-05 | 0.00287697 | missense | ERCC8 | GRCh38.p7 | 5:60903666 | GTAGAATGTGAGAAC[A/G]GGATCCAGACTTCAA | 1161 |
rs775026284 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913129 | GTTAGGGAGGATTCC[C/T]TCTTTTTCTATTGAT | 1161 |
rs775052484 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897251 | GAAACAGCAACTCCA[A/G]CGTCCCAGTATTTCC | 1161 |
rs775054029 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884068 | GCATTTGAAAGGAAA[C/T]CTAAGAATAACTTTG | 1161 |
rs775081196 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940939 | TGCATGGGAAAAGAC[-/A]AACAAAACAAGCCAA | 1161 |
rs775103568 | snp | A/G | 5.1989e-05 | 0.00509822 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945283 | CAGGATTTGTTCCGC[A/G]CCTTGTGGAGATCGC | 1161 |
rs775126943 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60890358 | GTGCAAATGTTCTCT[C/G]AAAAAATGAAAAACC | 1161 |
rs775144173 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885593 | AATATTCTGACACCA[A/G]AAGCAGCTGTATGCT | 1161 |
rs775188808 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60926752 | TCCCAAAACACTTTT[C/G]CTTCGTAATTAATCT | 1161 |
rs775203642 | snp | C/T | 1.65315e-05 | 0.00287498 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922132 | TAAAGTACAATCACA[C/T]CATCTGAACCACCTG | 1161 |
rs775222403 | in-del | -/AAAAAA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60909244 | AAATGCCCTATTCTG[-/AAAAAA]AAAAAAAAAAAAAAA | 1161 |
rs775226445 | snp | C/T | 1.64961e-05 | 0.00287189 | missense, intron-variant | ERCC8 | GRCh38.p7 | 5:60904851 | CTATAAACTGTTTCC[C/T]CAAAATTAAATACAT | 1161 |
rs775239317 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911345 | CATTTCTCTGATGAC[A/G]AGTGATGACGAGATT | 1161 |
rs775251931 | in-del | -/CTC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883411 | TTTTCTCTGCAACAT[-/CTC]CTCCTAGTGGACATG | 1161 |
rs775272984 | in-del | -/TGTATATATATATATATATATATATATA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904632 | TATAGTGTGTGTGTG[-/TGTATATATATATATATATATATATATA]TGTATATATATATAT | 1161 |
rs775280957 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925578 | GTTACTTTGGACTTA[C/T]CCAGGTATATCAGAT | 1161 |
rs775312066 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893986 | CCTGGGAATTTATCT[-/T]TTTTTTTTTTTTTTT | 1161 |
rs775379054 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920352 | TACTTTTAAATGAAA[C/T]AAATTTTTAATGTAG | 1161 |
rs775421502 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933162 | TTTAAATGGCTTTTA[G/T]AGGATGTATATTATA | 1161 |
rs775445181 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60896285 | GCAATGGCGCGATCT[C/T]GGCTCACCGCAACCT | 1161 |
rs775469167 | snp | C/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919039 | ACATAGTGTGTTACC[C/T]AACTGGATCTTGATT | 1161 |
rs775512860 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60941590 | AGAATGAACCCTAAC[C/T]AGGATAAATCCAAAG | 1161 |
rs775628302 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875080 | TACAGTCTGACCTGA[C/T]AGCCCAAAATATCAA | 1161 |
rs775718923 | snp | A/G | 1.7426e-05 | 0.00295173 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922019 | AATACTCAACTATTT[A/G]CAAATTCATAAATTT | 1161 |
rs775757701 | snp | G/T | 8.26549e-05 | 0.00642811 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887405 | ATTTCTTAAGCTTTA[G/T]AAGTCACTGTACCAT | 1161 |
rs775769269 | snp | A/T | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944993 | CCGTTTGGCGTGCGG[A/T]CAAAAACCCCAGCAT | 1161 |
rs775772552 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944055 | AAATTAAAAGTACAA[C/T]TTGCTTCTTCCCTTT | 1161 |
rs775811481 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889278 | ATTATATAAATATCT[C/G]ATTCCTCATCAAATT | 1161 |
rs775867078 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904693 | ATATATAAAATTGTG[-/A]TATTCCTCTGGGTTA | 1161 |
rs775948859 | snp | A/G | 1.65064e-05 | 0.00287279 | missense | ERCC8 | GRCh38.p7 | 5:60898358 | TGAAGTCCATCACTT[A/G]TAAAACATAAGCCAT | 1161 |
rs775978790 | in-del | -/AAA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60874701 | AAAAAAAAAAAAGAT[-/AAA]GAAAAAGGAAGATTC | 1161 |
rs776033048 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938650 | TGAGCCACAGCGCCC[A/G]GCTGAATTTGTTAAA | 1161 |
rs776074387 | snp | C/G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895478 | ATGATTTAACCACTT[C/G/T]GTTTCATTCTTCTTA | 1161 |
rs776147481 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935513 | TTCCTCTTTACTGAT[A/T]TGGGTGTCCTTGATT | 1161 |
rs776205031 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882291 | TTCCAAGTATCAGCT[A/G]GAAGAGCTGGAAAAC | 1161 |
rs776223191 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60942876 | GTGTTCATCCTTTTG[A/C]TCTTACATGATGACA | 1161 |
rs776260422 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925524 | CAGTTTGAGCTGCTG[C/T]AGTCAAATTTGCTTG | 1161 |
rs776338207 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914292 | TATTGGGTGCATATA[A/T]ATTTAGGATAGGTAG | 1161 |
rs776340089 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60922187 | TCACATTAATTTATC[A/G]TTTTATTTATTATTT | 1161 |
rs776375318 | snp | C/T | 2.03739e-05 | 0.00319163 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945208 | GGCTGGAGCATTACC[C/T]CTACTGCGGGTCCCG | 1161 |
rs776376333 | in-del | -/ACAA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940937 | CTTGCATGGGAAAAG[-/ACAA]ACAAAACAAGCCAAA | 1161 |
rs776397421 | snp | A/G | 1.7139e-05 | 0.00292732 | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945444 | GTCAGTAAAGGAGGG[A/G]AAAGTGAGAGCCCCT | 1161 |
rs776397428 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940982 | ACAAGTGTTGAGATT[A/C]TCTGATAAAGACTTC | 1161 |
rs776453112 | snp | C/G | 4.95552e-05 | 0.00497747 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922113 | GCTGGAGTTCTCAAG[C/G]TCATAAAGTACAATC | 1161 |
rs776527122 | snp | A/G | 1.74808e-05 | 0.00295637 | intron-variant | ERCC8 | GRCh38.p7 | 5:60922005 | CATTCGATGCAAAAA[A/G]TACTCAACTATTTAC | 1161 |
rs776530668 | snp | C/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918774 | TTCTATTAGCACTAC[C/T]ATTCTTAGAATTATT | 1161 |
rs776544820 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60887150 | TGTTCTTCTTTTGAT[A/T]TTTTTCTGAATTTTC | 1161 |
rs776548200 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936333 | GTAGCCTTGAATGAT[C/T]TTTTGTATTTCTGTA | 1161 |
rs776588097 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945202 | TCGGCGGCTGGAGCA[-/T]TTACCCCTACTGCGG | 1161 |
rs776663724 | snp | A/T | 2.19551e-05 | 0.00331317 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891125 | TACTCATCTCTGAAA[A/T]CTGAATTTAAAACAC | 1161 |
rs776689738 | snp | C/G | 6.89881e-05 | 0.00587276 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874602 | AGAGACAAAAAGGTA[C/G]TAAAGATGATATTCA | 1161 |
rs776780334 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897683 | AAATAAAGTACTACA[C/T]ATTCTGGTACTATAA | 1161 |
rs776792564 | snp | C/G | 3.30147e-05 | 0.00406279 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899732 | TACTGTCAGCACTGA[C/G]AAGAAATAAATGTTA | 1161 |
rs776834713 | in-del | -/T | 2.3853e-05 | 0.00345339 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874721 | AAAAGGAAGATTCTG[-/T]TTTTTCTACTTCATA | 1161 |
rs776841247 | snp | A/G | 1.65225e-05 | 0.00287419 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945374 | TCCCGCAGTACAAGA[A/G]CTGGAGAGGTGAGGT | 1161 |
rs776865615 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891934 | AGATCAGTCAATTAG[C/T]TACCAACACTGCCAT | 1161 |
rs776926864 | snp | A/T | 1.72585e-05 | 0.00293751 | intron-variant | ERCC8 | GRCh38.p7 | 5:60890840 | TTTACATATAACTGG[A/T]CTGGCAAGCTAGCTA | 1161 |
rs776955855 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60904100 | TATGTATGTATGTAC[A/G]GTTCTATTCCATTTT | 1161 |
rs776992717 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60939657 | ACCCGGAGCACGCCC[A/G]GCTGATTTTTGGATT | 1161 |
rs777076157 | in-del | -/TG | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60928336 | TTACGTTAATCATGT[-/TG]TGTGCATATTATCTC | 1161 |
rs777080077 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901509 | TTGCATCCTCATTCC[C/T]ATATTTTCAAGAGAT | 1161 |
rs777114091 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881916 | AACCTGGTACCTCAG[C/T]TGGAAATGCATAAAT | 1161 |
rs777163867 | snp | A/T | 1.66796e-05 | 0.00288782 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902397 | GACTTTTCAAAATGC[A/T]TATTATTAATTACTA | 1161 |
rs777177168 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925756 | TTTTCCTATTTGCCA[C/T]TTTTAGTCTCTTTAT | 1161 |
rs777268843 | snp | A/G | 1.66181e-05 | 0.00288249 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928818 | AGCAGGTTTTACTGC[A/G]TTTCACTTAGAAAGA | 1161 |
rs777300347 | snp | A/T | 1.6486e-05 | 0.00287102 | intron-variant | ERCC8 | GRCh38.p7 | 5:60887426 | ACTGTACCATTTGTG[A/T]AAATAATATTTACCT | 1161 |
rs777303378 | in-del | -/A | 1.65312e-05 | 0.00287495 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902549 | CTTGCAAGATATCTG[-/A]AAAATCAGAAGATAA | 1161 |
rs777308161 | snp | A/T | 1.69152e-05 | 0.00290814 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928992 | GAGAAAGAAATTAAC[A/T]AGTAATTTAACATTT | 1161 |
rs777373265 | in-del | -/TTTTGTTGCATTTATCTTTTGTG | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936470 | TTGAAAGAACCAGCT[-/TTTTGTTGCATTTATCTTTTGTG]TTTTGTTGTTGTTGT | 1161 |
rs777392638 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60902747 | TTGGAAAAAACAGAG[G/T]TAAGTAAGTCTTTCT | 1161 |
rs777392728 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888903 | ATGTTTCATTATTTG[C/T]TCCAATACTGTCCTT | 1161 |
rs777407519 | snp | C/T | 1.65293e-05 | 0.00287479 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922084 | ACTGCTTTACATGTG[C/T]AATAAGATTGTCTGC | 1161 |
rs777437387 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911136 | TACATAGGTATATAT[A/G]TGCCATGTTGGTTTG | 1161 |
rs777444521 | in-del | -/A | 0.0189359 | 0.0954788 | splice-acceptor-variant | ERCC8 | GRCh38.p7 | 5:60874685 | ATTTTGTTGTAGTCT[-/A]AAAAAAAAAAAAGAT | 1161 |
rs777463933 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60908345 | CATAGTGAGGCACAA[-/T]ATCTGTATATTCAGT | 1161 |
rs777470406 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907087 | CATCACCATAAAAGA[C/T]TATTCATTTCCTCTG | 1161 |
rs777485111 | snp | C/T | 6.60262e-05 | 0.00574532 | intron-variant | ERCC8 | GRCh38.p7 | 5:60902524 | CTGCAAATACAACTA[C/T]ATGAAAAGTCTTGCA | 1161 |
rs777488186 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889878 | AACAAATGGGATATA[C/T]CTTCTTATTGACTAA | 1161 |
rs777489532 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931481 | CTGGCTAAGTTTTGG[C/T]ATTTTTTTGCAGAGA | 1161 |
rs777513116 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881723 | AAAGTGCAGTATTAG[C/G]GTGGGAGTGACCCGA | 1161 |
rs777537158 | snp | C/T | 4.9516e-05 | 0.00497549 | missense | ERCC8 | GRCh38.p7 | 5:60898332 | GATTATCTGTACCAA[C/T]AGTGAGGAGGTGAAG | 1161 |
rs777552450 | snp | G/T | 3.37884e-05 | 0.00411011 | missense | ERCC8 | GRCh38.p7 | 5:60874672 | CGGATTTAATTGTGA[G/T]TTTGTTGTAGTCTAA | 1161 |
rs777600807 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925241 | GTAAGATTTCAAAAT[A/G]TGGAAGCTTACTTTC | 1161 |
rs777643535 | snp | C/T | 4.94931e-05 | 0.00497434 | utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945023 | TATCGTGTCCTCACA[C/T]CGGCTGGAGCACTGG | 1161 |
rs777679754 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940202 | TGGGTAATACTACTA[C/T]AAAAACTAAACAAAA | 1161 |
rs777786785 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918331 | TGTGAACATGCCAGT[A/G]TCATGAGGATACCAC | 1161 |
rs777838268 | snp | C/T | 1.65378e-05 | 0.00287552 | missense | ERCC8 | GRCh38.p7 | 5:60891022 | ACAAATTCTGAACTG[C/T]AGCCACAGGAGACAG | 1161 |
rs777877353 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60894898 | GATTTGTCGGCTGGG[C/T]GTGGTCTCACTCCCG | 1161 |
rs777880562 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901626 | TGTATTCATGTCCAC[A/C]TTTTCCTCTTTCCAT | 1161 |
rs777918748 | snp | C/G | 4.94849e-05 | 0.00497393 | missense | ERCC8 | GRCh38.p7 | 5:60899716 | TCCCATAATTTTACT[C/G]TACTGTCAGCACTGA | 1161 |
rs777941497 | snp | C/G | 1.76409e-05 | 0.00296987 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945270 | CATGGGTTGGTCTCA[C/G]GATTTGTTCCGCGCC | 1161 |
rs777957586 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60930039 | TGACATTAGTACAAG[A/T]AATTATAAGCATTTT | 1161 |
rs777964419 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60921593 | AAGACAGGGGTGAGT[C/G]GGTATATGTGTATGT | 1161 |
rs778085141 | snp | C/G | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917793 | CAAATGTCATACAAA[C/G]TATTATCCATTGCTT | 1161 |
rs778088340 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898093 | GTAGGGAGAATGTGG[C/T]AGGTAGTGGGTAAGG | 1161 |
rs778158081 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943831 | AAATGAGGAAAAGTG[A/G]TTGTGATGAAAGGCT | 1161 |
rs778163532 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, utr-variant-5-prime, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944965 | CTCCGAAGGCGAAGA[C/G]GGTCCTCCAAACCCG | 1161 |
rs778227577 | snp | C/T | 1.66272e-05 | 0.00288328 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918228 | TAAATTCTCCTTTAT[C/T]CTACAAAGCAATCTG | 1161 |
rs778254545 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891472 | CAAATGGTTTATTAA[G/T]GCAACCATTCTTTTC | 1161 |
rs778263229 | snp | G/T | 1.65405e-05 | 0.00287576 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945340 | GGCACGGACCAATTC[G/T]GGAACAAATACTACT | 1161 |
rs778344145 | snp | C/T | 1.79024e-05 | 0.0029918 | utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60874571 | AAAAACACAGTCTCA[C/T]TTAAAAAGTTTCAGC | 1161 |
rs778362430 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906852 | AATAATTAAGGCAGC[C/T]TGAAGGCTAAAGGCA | 1161 |
rs778380701 | in-del | -/TCATAAG | 3.35154e-05 | 0.00409348 | intron-variant | ERCC8 | GRCh38.p7 | 5:60903750 | TTTAAGATAATTTTA[-/TCATAAG]TCATCATCAAAAGGA | 1161 |
rs778401007 | snp | A/G | 1.67905e-05 | 0.00289741 | missense | ERCC8 | GRCh38.p7 | 5:60874659 | CATCTTCAAAGGCCG[A/G]ATTTAATTGTGATTT | 1161 |
rs778430020 | in-del | -/G | 1.6654e-05 | 0.00288561 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928972 | CTCTTAAAAATAAAA[-/G]GGGGGAGAAAGAAAT | 1161 |
rs778434319 | in-del | -/AAAAAT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886709 | CCATCTCAAAAAAAT[-/AAAAAT]AAAAATAAAAATAAA | 1161 |
rs778621303 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875488 | GGGAAAACTTCTGAA[C/T]AGCTACTTCTGATAC | 1161 |
rs778643408 | snp | G/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918475 | AAGTAGTAGTCTCAG[G/T]TAGGATGATATGAAT | 1161 |
rs778650550 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913921 | AGTTAGTTTCTTAAT[C/T]CTGAGTTCTAATTTG | 1161 |
rs778711158 | snp | A/C | 0.000265129 | 0.0115106 | | | GRCh38.p7 | 5:60928954 | TTTAATTCCAGTCCC[A/C]AAACTCTTAAAAATA | 1161 |
rs778724745 | snp | A/G | | | | | GRCh38.p7 | 5:60926593 | TTTAAAAAATATTCC[A/G]CATTAGCTTTATTAC | 1161 |
rs778731917 | snp | A/T | 1.66277e-05 | 0.00288333 | | | GRCh38.p7 | 5:60918402 | CTCTACAAAACAGCA[A/T]TCAAAATTTACATTA | 1161 |
rs778737089 | snp | A/G | | | | | GRCh38.p7 | 5:60905128 | AAAATATAAGCCTGT[A/G]GCTCACCATATTCCT | 1161 |
rs778841687 | snp | C/T | | | intron-variant, downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60903169 | TATTCTATCTTTTCA[C/T]TGTTTAGAATTAGAC | 1161 |
rs778897710 | snp | A/G | 1.64841e-05 | 0.00287085 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904766 | GTTTTCAGTATGTCA[A/G]AAGACAAAAGAATAC | 1161 |
rs778920677 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923890 | ACTCTTTCCTTTTCA[A/C]CTCAAAGTAACTCAT | 1161 |
rs778941225 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60897348 | CTGTCCATCTATTAA[C/T]TGATTGATGCCTTTC | 1161 |
rs779008824 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937510 | GGTTCCCAGGCCAAT[A/G]GAGTTATGTTCCCAG | 1161 |
rs779014777 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882735 | ACTGATTTCTAGCCA[C/T]GGTACACTTATTTGC | 1161 |
rs779070115 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60924919 | ACTTAACATTATTCT[C/T]TCATTTATTATATGT | 1161 |
rs779109084 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60917366 | AAAACTGGTAGAACA[C/T]AGGATTGAAGGAACA | 1161 |
rs779113988 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910583 | TTCTCTGTGTATTCG[A/G]AATAGTCTTGTATAT | 1161 |
rs779199928 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895990 | ATATTTCTTTTCTTT[C/T]CTTTTCTTTTTTGAG | 1161 |
rs779219481 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886681 | CACTCCAGCCTGGGC[A/G]ACAGATTGAGACTCC | 1161 |
rs779309100 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888483 | GGTCAGATAAGCTTA[C/T]AGAGCAATTCACAAT | 1161 |
rs779379627 | snp | A/G | 1.65236e-05 | 0.00287429 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898408 | AGTGTTTGCTGCAAT[A/G]AAAAACATAGTTCAG | 1161 |
rs779417084 | snp | C/T | 0.000181808 | 0.00953263 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945252 | TGGAAACTGGGTGGA[C/T]GGCATGGGTTGGTCT | 1161 |
rs779476152 | snp | C/G | 1.64917e-05 | 0.00287151 | missense | ERCC8 | GRCh38.p7 | 5:60899702 | ATGCTCTTCTCACAT[C/G]CCATAATTTTACTCT | 1161 |
rs779504739 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60898627 | AAAAATTTCTGCCTA[A/G]CATACTTTTCTTTTC | 1161 |
rs779511403 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60911715 | CTTCTGGGGTTTTTA[C/T]GGTTTTAGGTCTAAC | 1161 |
rs779562953 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60940100 | CTCCTAATCTCTTAT[C/T]ATTTTCATTACTGGT | 1161 |
rs779673414 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927936 | TTCTGACTTGACTTA[A/C]TGTATTAATAATAAT | 1161 |
rs779813259 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60886570 | AGCCAGGCGTGGTGG[C/T]GGGTACCTGTAATCC | 1161 |
rs779849995 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60936197 | TTTCAATCTCATTGC[C/T]TGTTGCTGGTCTGTC | 1161 |
rs779870704 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60892956 | TAGTTCCCCAGAACC[C/T]TCATGAGGTTTTCAG | 1161 |
rs779872068 | snp | A/G | 3.30568e-05 | 0.00406538 | upstream-variant-2KB, missense | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945353 | TCGGGAACAAATACT[A/G]CTACATCCCGCAGTA | 1161 |
rs779944382 | snp | A/G | 1.73255e-05 | 0.0029432 | upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945082 | GACTGGAACAGCAGA[A/G]TCTCCCATTGGTCAG | 1161 |
rs779968300 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60891771 | TTGGGACTCTTTTTC[C/T]TGGAGAGAGTGGAGA | 1161 |
rs779993885 | snp | A/G | 4.9552e-05 | 0.0049773 | synonymous-codon, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928938 | AACATCTCTGTCTTT[A/G]TTTAATTCCAGTCCC | 1161 |
rs780058348 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875617 | ACTACAATTTTATTC[A/T]GATTCCAATTCCAAT | 1161 |
rs780104224 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934576 | AGTTTAATTAAGACC[C/T]ATCTATTTATCTTTG | 1161 |
rs780135206 | snp | A/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946322 | AAAGTTAGAGATAAT[A/G]TAAGATCAGCAATGT | 1161 |
rs780151767 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925115 | TCCTTTGCTCATTTT[A/T]ATGTAAAATTAATTT | 1161 |
rs780224304 | snp | A/G | 2.00367e-05 | 0.00316511 | intron-variant | ERCC8 | GRCh38.p7 | 5:60891105 | TAGGATTAAAATAAT[A/G]AGGTTACTCATCTCT | 1161 |
rs780244684 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60889666 | TTTGGTAGAAAGAAA[C/T]AATTTGTGGTTAGAG | 1161 |
rs780247377 | snp | C/T | 1.90304e-05 | 0.00308461 | upstream-variant-2KB, utr-variant-5-prime | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945228 | TGCGGGTCCCGCTGC[C/T]GGCAGCGCTGGAAAC | 1161 |
rs780254614 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60882772 | TGTATACTGAAGTCT[A/G]TTCATTTTGTCTTTC | 1161 |
rs780302746 | snp | C/T | 1.64846e-05 | 0.0028709 | intron-variant | ERCC8 | GRCh38.p7 | 5:60904755 | AAAGGGAGAAAGTTT[C/T]CAGTATGTCAAAAGA | 1161 |
rs780364709 | snp | A/G | | | intron-variant, downstream-variant-500B | ERCC8, LOC105378991 | GRCh38.p7 | 5:60919733 | TGGAAAAATGAACAT[A/G]ACCTTGAAATGGAGC | 1161 |
rs780412955 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60910783 | ATAGATTCTTTTGAA[-/T]TTTTCTACGTTCATA | 1161 |
rs780454386 | snp | C/T | | | intron-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918556 | AGAATGTCCAGGCAT[C/T]TCTAGATTCAGGCTC | 1161 |
rs780499829 | snp | A/C | 1.65721e-05 | 0.0028785 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60922064 | CATACCTGCCAATGG[A/C]ACACACTGCTTTACA | 1161 |
rs780533651 | snp | C/T | 3.30431e-05 | 0.00406454 | missense | ERCC8 | GRCh38.p7 | 5:60898316 | TTCCAGAGCCTCATT[C/T]GATTATCTGTACCAA | 1161 |
rs780598708 | in-del | -/TA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914473 | CTTTTATTTTGAGCC[-/TA]TGTGTGTCAGTATGC | 1161 |
rs780622875 | snp | C/T | 4.95029e-05 | 0.00497484 | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928922 | CGCCGTGGATTCTTT[C/T]AACATCTCTGTCTTT | 1161 |
rs780635843 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912499 | ATTTTGGGCTCAGAC[A/G]ATGGGGTTTTCTAGA | 1161 |
rs780673930 | snp | A/G | 6.59478e-05 | 0.00574191 | missense | ERCC8 | GRCh38.p7 | 5:60899689 | ATCAAACATCCTGAT[A/G]CTCTTCTCACATCCC | 1161 |
rs780682704 | snp | G/T | 1.65559e-05 | 0.00287709 | intron-variant | ERCC8 | GRCh38.p7 | 5:60928842 | AGAAAGAAAAATGAT[G/T]ATACAAGTATAATAA | 1161 |
rs780695095 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60925724 | GACCTAGTTTGGTTG[-/T]TAAGTGTTAATCTGG | 1161 |
rs780794576 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881454 | CTATGCCGTGCCCCC[-/A]GAGGTGAAGTCTACA | 1161 |
rs780809500 | snp | C/T | 1.65482e-05 | 0.00287643 | intron-variant | ERCC8 | GRCh38.p7 | 5:60898435 | TCAGTTTATCTGTTC[C/T]TGTATTCAGGACATA | 1161 |
rs780839675 | in-del | -/T | 1.6897e-05 | 0.00290658 | frameshift-variant | ERCC8 | GRCh38.p7 | 5:60874671 | CGGATTTAATTGTGA[-/T]TTTTGTTGTAGTCTA | 1161 |
rs780915660 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60888780 | ACATTAGGCCTTACT[A/C]CTCTTGAATAATTCA | 1161 |
rs780936771 | snp | A/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893270 | TCCAGCTGAGGAAAC[A/T]TATTTAATTCCTGCA | 1161 |
rs780995423 | snp | A/G | 2.07084e-05 | 0.00321773 | intron-variant | ERCC8 | GRCh38.p7 | 5:60874698 | TCTAAAAAAAAAAAA[A/G]ATAAAGAAAAAGGAA | 1161 |
rs780999696 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923978 | ACCTTAGAGTGTACA[C/T]ATGAATATTAGCTTT | 1161 |
rs781012433 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60937662 | ACTGCGCCCCTACAA[C/T]AGCTCTGAGTTTATT | 1161 |
rs781024613 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60878832 | CAGCTCCTGGATTCA[C/T]TGATTTTTTGAAGGG | 1161 |
rs781060715 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929281 | TTCCTTGAAATGTTT[C/T]TTAAAGACGGACAGA | 1161 |
rs781073237 | in-del | -/C | | | downstream-variant-500B | ERCC8 | GRCh38.p7 | 5:60873506 | ATGGTGAAACCCCAT[-/C]TCTACTGAAAATACA | 1161 |
rs781081565 | in-del | -/A | 0.000133369 | 0.00816497 | intron-variant | ERCC8 | GRCh38.p7 | 5:60899581 | AAAAATTTTCAATGT[-/A]AAAAAATACTATCAT | 1161 |
rs781118831 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881654 | GGGCGTCGGACCCTC[C/T]GAGCCAGGCGCAGGA | 1161 |
rs781129159 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931119 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGC | 1161 |
rs781296399 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60906875 | TAAAGGCAAGAGGGG[A/G]TGGTGGCTAGATCAG | 1161 |
rs781297220 | snp | G/T | | | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60916459 | TTCTTGGCAGCTTTA[G/T]AAAACCCTCAACTAG | 1161 |
rs781297753 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60885151 | TAAGTAGCTGGAACT[A/G]TAAGTGTAAAGCCAC | 1161 |
rs781320471 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60913811 | TTGTTCTCATTGGTT[C/T]CAAAGAACATCTTTA | 1161 |
rs781326929 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60905467 | CAATATCTGCAATTC[C/T]TTTGCTAACATCCTT | 1161 |
rs781341530 | snp | A/G | 4.97954e-05 | 0.00498951 | intron-variant, upstream-variant-2KB | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918257 | TGCAAATGTTTTAAT[A/G]TACTTACTTGTAATG | 1161 |
rs781344883 | snp | C/T | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945874 | CGCCTCGGCTGTCTT[C/T]TTTCTTGGTGTTTAC | 1161 |
rs781376884 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60934805 | AATTGTCCCAGGACT[A/G]TTTGTTGAATAGGGT | 1161 |
rs781390385 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60935122 | TTTGTAGATTGTTTT[G/T]GGCAGTATGGTTATT | 1161 |
rs781472404 | snp | C/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60921220 | TAATGCGAAACACCA[C/G]AGCCAACAAACAATA | 1161 |
rs781484832 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893438 | ATTTCAGCCTCTCGA[C/T]TGGCATGATCATTGG | 1161 |
rs781518798 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912623 | GCCAGAACTTCCAAC[A/G]CTATGTTAAATAGGA | 1161 |
rs781538504 | snp | A/C | 4.11836e-05 | 0.00453763 | intron-variant, utr-variant-3-prime | ERCC8 | GRCh38.p7 | 5:60903532 | CCTGCTGAGTCTCAA[A/C]AACCAGCACAAAGTA | 1161 |
rs781560448 | in-del | -/A | 1.65444e-05 | 0.00287609 | upstream-variant-2KB, frameshift-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60945335 | ACGTGGGCACGGACC[-/A]ATTCGGGAACAAATA | 1161 |
rs781641016 | in-del | -/TACTTC | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901214 | TTAGTCTAACTCTCA[-/TACTTC]TACTTCATTAGATCC | 1161 |
rs781672060 | snp | A/C | 3.31323e-05 | 0.00407002 | missense, utr-variant-5-prime, nc-transcript-variant | ERCC8, LOC105378991 | GRCh38.p7 | 5:60918360 | ACTGTACAGTCTCCA[A/C]ACTGTATCTGTGAAC | 1161 |
rs781699664 | snp | G/T | 3.52175e-05 | 0.00419613 | missense | ERCC8 | GRCh38.p7 | 5:60891073 | CTGTTATTACAAACT[G/T]TTCCATAGTTCACCT | 1161 |
rs781709549 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60920214 | TAAGTCTGATTCTCC[A/C]ATCTTCCTGACAGTT | 1161 |
rs781762912 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907080 | GTGTGACATCACCAT[-/A]AAAAGATTATTCATT | 1161 |
rs786205176 | in-del | -/C | | | frameshift-variant, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928896 | CGGCGGTGGAATTAA[-/C]ACCCTTGACATTGAA | 1161 |
rs786205573 | snp | A/G | | | missense | ERCC8 | GRCh38.p7 | 5:60890914 | ATAAAACTGTTGACT[A/G]CTGTGTATTTCAGTC | 1161 |
rs794727233 | snp | A/G | | | missense, utr-variant-5-prime | ERCC8 | GRCh38.p7 | 5:60928910 | GTTGAAAGAATCCAC[A/G]GCGGTGGAATTAACA | 1161 |
rs796092162 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884454 | GCACTCCAGCCTGGG[C/T]GACAGAGCCAGACTC | 1161 |
rs796124508 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881537 | CCAGCCGCTTTGTTT[A/G]CCTACTCAAGCCTCA | 1161 |
rs796127029 | in-del | -/AT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60883005 | CACACACACACACAC[-/AT]GTCTGTAGGTGGATA | 1161 |
rs796141277 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60944137 | GCATAGATCTGGGAA[-/GA]ATTATTCATTCTTCT | 1161 |
rs796321796 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933216 | TTTTTCCTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 1161 |
rs796379883 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929870 | TATTAGCATCTACAC[C/T]AATTTAACCAGAATT | 1161 |
rs796383948 | in-del | -/AA | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60914808 | AAAAAAAAAAAAAAA[-/AA]GGATATTGACTTTTA | 1161 |
rs796404319 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907253 | GAAAATAGGAGGCAG[G/T]CAATCAGAATTTCCT | 1161 |
rs796407596 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933208 | GTATGCATTTTTTCC[-/T]TTTTTTTCTTTTTTT | 1161 |
rs796412237 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884355 | GTGGTGGGCGCCTGT[A/G]GTCCCAGCTACTCGG | 1161 |
rs796415108 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60881972 | TGGGAGCTGCAGACT[G/T]GAGCTGTTCCTATTC | 1161 |
rs796427911 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884344 | AGCTGGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 1161 |
rs796450175 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60943701 | TAAATGGAGCAAATG[-/A]AAAAAAAAGCTGCCT | 1161 |
rs796450592 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60929852 | TCTTAATCTGTTGGC[C/T]GTTATTAGCATCTAC | 1161 |
rs796480290 | snp | G/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60884471 | ACAGAGCCAGACTCC[G/T]TCTCAAAAAAAAAAA | 1161 |
rs796529137 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60931681 | ATATTTCATCAAAAC[-/T]TTTTTTTTTCATATT | 1161 |
rs796555125 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875796 | CCGCCTCCCGGGTTC[A/G]CGCCATTGTCCTGCC | 1161 |
rs796566139 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901835 | CTCTTTTTCTCCAGC[-/A]AAAAAATAAACCTCC | 1161 |
rs796574343 | in-del | -/G | | | upstream-variant-2KB, intron-variant | ERCC8, NDUFAF2 | GRCh38.p7 | 5:60946890 | AAATGGAATTATACA[-/G]GATTTAGACTTTTGA | 1161 |
rs796750386 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60938350 | AGCTACCTTTTTGAA[-/T]TTTTTTTTTTTTTTT | 1161 |
rs796828517 | in-del | -/TACT | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60901127 | TAATAATTCTTCTTC[-/TACT]TAAAGTTTTATGAAA | 1161 |
rs796849964 | in-del | -/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60923094 | CAGGAGCCAAACCAC[-/G]TGAAGCCTTACTTTT | 1161 |
rs796901783 | in-del | -/A | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60927105 | AAATTCAAGCTTCAC[-/A]AGAGTGATACGCAAA | 1161 |
rs796906404 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60933220 | TCCTTTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 1161 |
rs796907912 | in-del | -/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60895440 | TTTTAAACACTCATC[-/T]TTTTTTTTGCCCCTT | 1161 |
rs796917187 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60875315 | AACATGCAAAATACG[C/T]CAGAAATGGTAACAC | 1161 |
rs796926395 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60912749 | TAAATAGCCCTTATT[A/G]TTTTGAGATACATTC | 1161 |
rs796948677 | snp | A/G | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60876109 | GTTCAATTCCCACCT[A/G]TGAGTGAGAACTTGG | 1161 |
rs796974674 | snp | A/C | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60899791 | TGTACCCCTCACCCA[A/C]CTTTCTAATTTTATG | 1161 |
rs797006567 | snp | C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60893132 | CCATAGGATAGCCTC[C/T]CCCATTTGGAAGCAG | 1161 |
rs797011876 | snp | A/C/T | | | intron-variant | ERCC8 | GRCh38.p7 | 5:60907355 | CATAGAAACATGATT[A/C/T]TTTTTTTTTTTTTTT | 1161 |