SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs146616092 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512038 | ATGCTATAACAGTTG[A/G]CAGATTACACAAAAA | 2074 |
rs146652638 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499644 | TATCTGGGTTCAGTA[C/T]GATGAAATATCCTAC | 2074 |
rs146664460 | snp | C/T | 0.000149632 | 0.00864833 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49517094 | GTCAGTTATTTCATG[C/T]AAACTTAGTGTTCGA | 2074 |
rs146671715 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505748 | GCTATAATTTCATTT[A/G]ACAGTATCTGTTTTT | 2074 |
rs146690522 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455535 | GCGTGAGGAGTGTGG[C/T]TGGTAGAACCAACAC | 2074 |
rs146773818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523580 | CTTATTCTTTCTATG[C/G]CAAAGCTTAAGTTTC | 2074 |
rs146786861 | snp | A/C/T | 4.94444e-05 | 0.00497194 | missense | ERCC6 | GRCh38.p7 | 10:49474062 | GCAATACTCGCTGAC[A/C/T]CTGCTTGTGCCATAT | 2074 |
rs146793319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527606 | CTTGAACCCGGGAGG[C/T]AGAGGTTGCAGTGAG | 2074 |
rs146871654 | in-del | -/CT | 0.100231 | 0.200173 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536108 | GCAACAAGAGTGAAA[-/CT]CTGTCTCGAAAAAAT | 2074 |
rs146948664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528774 | ATGCTCTCCTGAGGA[C/T]GGCAGACTGCCTTCT | 2074 |
rs147079519 | snp | C/G/T | 0.00133373 | 0.0257896 | missense | ERCC6 | GRCh38.p7 | 10:49470569 | CTGTTCCTGAAGAAT[C/G/T]TGAACATTCCCCATT | 2074 |
rs147121546 | snp | C/T | 0.000248388 | 0.0111415 | missense | ERCC6 | GRCh38.p7 | 10:49472943 | TTCCAGTCTGGGTCA[C/T]AGATGACAACTCTGT | 2074 |
rs147214586 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526362 | AATAGGTGCCTTTCA[C/T]GAATTTATCTTTTGG | 2074 |
rs147228327 | in-del | -/AAT | 0.067446 | 0.170804 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456849 | AGGAGGCACGGTAAC[-/AAT]GTGTCAGATCTCCAC | 2074 |
rs147231237 | snp | C/T | 3.30098e-05 | 0.00406249 | missense | ERCC6 | GRCh38.p7 | 10:49476244 | TGAGAATCCTGTAAA[C/T]TTCTTTGGAATCAAC | 2074 |
rs147242124 | snp | C/T | 0.00019772 | 0.00994086 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516703 | TGGGAGTTCTCATTA[C/T]GGTGAAGAAATCGTT | 2074 |
rs147246818 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503469 | ACTAGGGATAGTTAC[A/T]AAGATAGCAAAGAGT | 2074 |
rs147251562 | in-del | -/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517628 | ACACAGTCTTCTTTC[-/T]TTTTTTTTTTTTCTC | 2074 |
rs147284198 | snp | A/T | 9.90034e-05 | 0.00703505 | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524239 | ATAGTCAGTACCATC[A/T]CCAGACAGGTCCGCC | 2074 |
rs147337903 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495064 | CCTCCTGCCCTTCTG[A/G]GACAAAGGGACAGTG | 2074 |
rs147353500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525474 | ATATGTGAAGTTAAC[G/T]GACTTGAAGACATTA | 2074 |
rs147441836 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521150 | TGCAGACATGCATTG[C/T]TGACATGAAAGCAAA | 2074 |
rs147503108 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489543 | CACAAAACCAATGCA[C/T]TTAAAACTGCATGCT | 2074 |
rs147548816 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454026 | GTTTTCAGTCATTGT[A/G]TCTTTAAATATTTCC | 2074 |
rs147587749 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531758 | CCACATTCATGACAG[C/T]GCCACACTCCACCCT | 2074 |
rs147620907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468618 | GTGCATATATATGCA[C/T]GTATGTATGTGTATA | 2074 |
rs147621129 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521629 | GGCTCATCCATCCTG[C/T]ATGACATGAAAGGGT | 2074 |
rs147637331 | snp | A/T | 0.00071635 | 0.018912 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471128 | AGATTTGTCTAAAAA[A/T]ATAAAAGATAAGCTG | 2074 |
rs147708951 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537117 | TTGGGAGGCCGAGGC[A/G]GGAGGATCACGAGGT | 2074 |
rs147740542 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491860 | TGTTAACAGATAACA[G/T]AAATGAAAAAGGAAC | 2074 |
rs147792874 | in-del | -/AACAG | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525768 | GCAGCCATATCAACT[-/AACAG]AATTACTAGCACCAC | 2074 |
rs147828728 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511808 | ACAACAGACACAGAT[G/T]TAAGATAACCACAGA | 2074 |
rs147838944 | snp | A/C | 4.94254e-05 | 0.00497094 | missense | ERCC6 | GRCh38.p7 | 10:49532851 | CTCCTCCACCTCCCC[A/C]TCACCACCACTTTCT | 2074 |
rs147845123 | snp | C/T | 0.00193881 | 0.0310748 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515287 | CTGCTACACTGTACA[C/T]AATGTATAAAACTAT | 2074 |
rs147919817 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492213 | AGGAATCCTGGAGTT[G/T]CGTGGTCCCCGTGCA | 2074 |
rs148032008 | snp | A/C | 0.000307953 | 0.0124049 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516272 | AATAAATTGTTTGCA[A/C]CCGTGACGACCAAAA | 2074 |
rs148095899 | snp | A/G/T | 0.00136755 | 0.0261133 | synonymous-codon, missense | ERCC6 | GRCh38.p7 | 10:49532565 | CATCCAGGACCGACC[A/G/T]ATACTCCTTCTCCAC | 2074 |
rs148107759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469268 | CCTGGCAGACTCCAC[C/T]TTAACCAAGTGATCT | 2074 |
rs148112322 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503179 | AAGTAGGGAGAGTGC[A/G]GAAAGGAGCAGTTGA | 2074 |
rs148149838 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523874 | TAAGGACTCAGGGGC[C/G]CCACTGCTTCTAGCA | 2074 |
rs148180541 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531986 | CCATTAACGTGCTAT[C/G]CTCAAAACAGCTCAA | 2074 |
rs148208319 | snp | G/T | 0.000439464 | 0.0148168 | missense | ERCC6 | GRCh38.p7 | 10:49474079 | TGCTTGTGCCATATT[G/T]TCAACAAAGACTCAA | 2074 |
rs148295935 | snp | C/T | 0.000463976 | 0.0152241 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524271 | CTGCCCCCTCCACCT[C/T]GTCATCTTCCTCCTC | 2074 |
rs148308646 | in-del | -/AT | 0.0107246 | 0.0724382 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463030 | AAAATCTAAATCCTC[-/AT]ATGTGGATAAACTGT | 2074 |
rs148338960 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528147 | TTAACAAAATAAGAA[C/T]GTTTAAGATTTCCAG | 2074 |
rs148355291 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479076 | TGGTTCTGTAATGGA[A/G]CACGGCCACATGAGA | 2074 |
rs148366188 | snp | A/C | 0.00217473 | 0.0329035 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470504 | TCTTTTGTAAGAAAG[A/C]CCTAACTTTTCATCA | 2074 |
rs148375725 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466444 | TGAAATTGGAGACAA[C/G]AGTATTCCCTCATCT | 2074 |
rs148412211 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475762 | TTTATATCTGGTTCC[C/T]AACATGGCAATGGTT | 2074 |
rs148417688 | in-del | -/TTTATATATATATATATATATATATATA | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526116 | ATATATTTATATATT[-/TTTATATATATATATATATATATATATA]TATATATATATATAT | 2074 |
rs148447488 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529968 | CTAAGTACAACCCCA[A/G]TGTGGCTGGGTGCTG | 2074 |
rs148463831 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481231 | GTTTGCAAAATGCTA[A/C]CAATCAGTGAATCTG | 2074 |
rs148475034 | snp | C/T | 0.000757738 | 0.0194498 | missense | ERCC6 | GRCh38.p7 | 10:49470773 | ATGTGGCATCATTTA[C/T]AGATATGTTAGAAGC | 2074 |
rs148551761 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498379 | TTCATTTGACCTTAA[C/G]AGCTATTTTTCTGTA | 2074 |
rs148587807 | snp | G/T | 4.94368e-05 | 0.00497152 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516740 | TGCTGTAACTCTACC[G/T]GCTACGGGTTGTACA | 2074 |
rs148609302 | in-del | -/AAC | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461099 | TCTCTTACTATTTTT[-/AAC]AACACCATCTCTCAA | 2074 |
rs148624868 | snp | A/G | 0.000148252 | 0.00860837 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532818 | CAGCCCGTCACCCAC[A/G]GAACGAAAGGAGAGG | 2074 |
rs148636026 | snp | C/G | 0.00112158 | 0.0236544 | missense | ERCC6 | GRCh38.p7 | 10:49470478 | TCTGTTTGAGCCTGG[C/G]TGGGTCTTTCTCTTT | 2074 |
rs148671589 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526928 | GCCATGGGGAATAGA[C/T]AACCAGGGAGAGGCA | 2074 |
rs148736072 | snp | C/T | 0.000307953 | 0.0124049 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49478405 | GACATCTGACTTCAT[C/T]CTCCGCAGTAGGTAT | 2074 |
rs148761654 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534155 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAACTCCA | 2074 |
rs148762958 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454743 | TTATATCAATATATA[C/T]CAGAAAAGACTTTGA | 2074 |
rs148819321 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537815 | GCAACCTCCGCCTTC[C/T]GGGTTCAAGCGATTC | 2074 |
rs148845653 | snp | C/T | 0.000675425 | 0.0183645 | missense | ERCC6 | GRCh38.p7 | 10:49482808 | AGCGACCACAGCTCT[C/T]GGAGGTTATTTTGCA | 2074 |
rs148851684 | snp | A/G | 3.33233e-05 | 0.00408173 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524707 | TGTCATCTGGCCAGT[A/G]CGGATGAGCTCTTCC | 2074 |
rs148905772 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468178 | TTTTCTTGCACAATG[C/T]GCTGGTCAGTATTCA | 2074 |
rs148956291 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517406 | CATGCCAGTATCTGT[A/C]GCAGTAACTAACTCT | 2074 |
rs148993084 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481939 | CCCTCTTGTGACTAC[A/C]CTGTAGCCTGAGGAA | 2074 |
rs149024968 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462602 | AACATCCCTAATATA[C/T]AAAGAACTCTTTAAA | 2074 |
rs149113739 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511183 | GCTGATGGAAAGAAC[A/C]AGGAGCCCTGAGTTT | 2074 |
rs149150757 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522679 | TAATTGGAAAAATAT[A/G]TATTGCTCCATTTAT | 2074 |
rs149167061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471941 | AACAGCCATCCTGTC[A/G]ACTTCTTTGTAAGGG | 2074 |
rs149203330 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528014 | TTCTTAAACTGATGC[C/T]TGGAAAGCCTGCCAA | 2074 |
rs149277512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475448 | AAGACCTGAAGAAGT[C/T]AAGGGGAGATTCATG | 2074 |
rs149294198 | snp | A/G | 0.0158469 | 0.0875917 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456696 | GTGCTGATAAAGCAT[A/G]TTAAATACATTAAAT | 2074 |
rs149312554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529679 | GTGAACTGAACCAAC[A/G]CACAGCCCTGCCCCT | 2074 |
rs149349136 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539595 | TTGCCTTAAGTCCAG[C/T]GTTTAGTATCCGTCC | 2074 |
rs149366005 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491135 | TTATGATCTTAGAAA[C/T]GTCAATAGTAAGGCC | 2074 |
rs149382642 | snp | A/G | 0.000708314 | 0.0188057 | missense | ERCC6 | GRCh38.p7 | 10:49530832 | TGCCTTAGGGATGTC[A/G]TACATGACCTGAAAA | 2074 |
rs149431274 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469770 | CCTTGACATAAGCTA[A/T]CAGCTTTCATACTTC | 2074 |
rs149488489 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519651 | GGGTGGGCATGGGTC[A/G]GGGATTTATCCCAGA | 2074 |
rs149505457 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502907 | ATGAACTGGCTACAC[C/T]AGAATAATCTCAACT | 2074 |
rs149526654 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483703 | CTGACTAATACAGCC[A/G]TTATTAGGGGAAGGA | 2074 |
rs149556678 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462498 | ACTGACAATTTTTTT[-/A]AAAAAAAAACCTGTT | 2074 |
rs149558496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466122 | TGTATTTTAAACTGA[C/T]AGCACACACTGAAAA | 2074 |
rs149645921 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512643 | TCCAAAATGCTTGGG[A/C]CAAGAAGTGTTTTGG | 2074 |
rs149666343 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467774 | GGATCTCACTATGTT[G/T]CCCAGGCTGGTTTTG | 2074 |
rs149755223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49515069 | TTTGTGTCTCAGCTT[C/T]GTTATTTAAAAGAAG | 2074 |
rs149801805 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477926 | CAACCCTGCTTCATT[C/T]GTCTCCACACTTAAT | 2074 |
rs149814384 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474752 | TATTATTATATCAGA[A/G]AAAAAACTGCATGAA | 2074 |
rs149818939 | snp | A/C | 0.00421576 | 0.0457177 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460482 | CATCACAGTAGATTA[A/C]ATGTTTGCTTTTGAG | 2074 |
rs149844461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531264 | TTAAACATTTTTTTA[C/T]ATAAATCACACATCT | 2074 |
rs149850296 | snp | A/G | 0.00210713 | 0.0323902 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516729 | TCGTTTGGTGGTGCT[A/G]TAACTCTACCTGCTA | 2074 |
rs149860966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481903 | CCCCAGTGGTTCCTG[A/C]AGGTCACTCAGTGCC | 2074 |
rs149876669 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510919 | CCTAGCTCTGTCCAC[C/T]GGATAAAAATGGTTA | 2074 |
rs149914413 | snp | A/G | 0.000115313 | 0.0075923 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532809 | AGAGGTGGACAGCCC[A/G]TCACCCACAGAACGA | 2074 |
rs150051412 | snp | A/C | | | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454167 | TTCTTTGGAAAGCAT[A/C]TCTCTCTTATTCTAT | 2074 |
rs150065567 | snp | C/T | 8.24002e-05 | 0.0064182 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524450 | ATGTGCTTTTTCAAA[C/T]GCTCCTCTTTTTTGG | 2074 |
rs150106294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537475 | CTCATGGGAAAAACA[A/G]ACATTTAAAAACTAT | 2074 |
rs150190458 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469479 | GAGTTCTTCGTATTA[C/T]TCCAACTGATTTTTT | 2074 |
rs150248248 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475061 | CAGGAACATTGGTAA[A/T]CCTCCCCAGAGTCAT | 2074 |
rs150277901 | snp | A/G/T | 0.000511246 | 0.0159806 | missense, synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459202 | AAAATGCTCAGGGAC[A/G/T]TTATCTTTTCCCTCC | 2074 |
rs150316892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492452 | GATATAAAAATGAAT[C/G]AGACACAGTCCCTAC | 2074 |
rs150320544 | snp | A/G | 0.000197808 | 0.00994307 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515855 | ACCAGATGAGGCAAC[A/G]GTGACAACACTGTTA | 2074 |
rs150405562 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512549 | AAGTATGAAAGGTAC[C/T]AAAAGCATAACATCA | 2074 |
rs150509892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513712 | TAACTATCGTGAGAA[C/G]AGCATGGGGGAAACC | 2074 |
rs150563685 | snp | A/G | 1.65622e-05 | 0.00287764 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516454 | ATATAGTTTCAAACC[A/G]GTCACGTCTCATGGC | 2074 |
rs150601079 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529608 | GCAAGTGAGAGAAGA[C/T]GGGGTAGTGCAGGTA | 2074 |
rs150637470 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539418 | GTCAGCTTGGGCAGG[G/T]AAGTTAGCCGCACTT | 2074 |
rs150650983 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527533 | TACAAAAAATTAGCT[A/G]GGCATGGTGGTATGC | 2074 |
rs150762517 | snp | A/G/T | 9.92218e-05 | 0.00704287 | missense, synonymous-codon | ERCC6 | GRCh38.p7 | 10:49505928 | CACTTTAAAACCTTC[A/G/T]TCAAATTCAGCATCA | 2074 |
rs150801494 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506726 | TCTTAGCAATACACC[-/A]AGGTTGTGGAGAAGG | 2074 |
rs150804833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483050 | TTAGATGAAAAAATG[A/G]GAAAGAATTTTTTCT | 2074 |
rs150862843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481524 | GAGAGCTTCCCTTTT[A/G]GTGGAAGGTCTCATC | 2074 |
rs150901215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503966 | TTTGTCATTTGACTG[C/G]TAAATTAGATAGACA | 2074 |
rs150935953 | snp | A/G | 0.000528528 | 0.0162476 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524760 | TGAGCATGCTGCCAA[A/G]ACTGGATGGCCCCGG | 2074 |
rs150951870 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499283 | TATAAATGCAACTGG[C/T]GTTCTAAAATATTCT | 2074 |
rs151216994 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464012 | TCCCAAAATGTGGAA[G/T]CAACTTTGGAACTGG | 2074 |
rs151242354 | snp | A/G | 8.28782e-05 | 0.00643679 | stop-gained | ERCC6 | GRCh38.p7 | 10:49482689 | CCTAATATTTTACCT[A/G]TACTGGGGAAGCATT | 2074 |
rs151293836 | snp | C/T | 6.59413e-05 | 0.00574163 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515778 | TTTGGCTGCTGAACT[C/T]GTATCTTCTTTTTCA | 2074 |
rs151320079 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535158 | TAATAAAAAGTTTGG[C/T]CTGGACAAATGAGTC | 2074 |
rs151336505 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486793 | GGTTTTATGAGTAAA[A/G]TAGGACTAGATCCTA | 2074 |
rs180719898 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49541030 | GCTTAAACAACAGGC[A/G]TTTGTTTCTCATAGT | 2074 |
rs180838201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465472 | GACTTTAGGGGACTG[C/T]TGGGAAGGCATGATT | 2074 |
rs180966134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463162 | CATCTTGGGGATGGG[C/T]CCCAAGTCTAAACAC | 2074 |
rs181050647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532243 | CCTGAATTTAGGTGC[A/G]CCTCTCCTGAGATCA | 2074 |
rs181055741 | snp | A/T | 0.00011533 | 0.00759287 | intron-variant, stop-gained | ERCC6, PGBD3 | GRCh38.p7 | 10:49515608 | TCTCATCATATGTTT[A/T]ATGCAATTGCCAAGC | 2074 |
rs181070955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499010 | AGAGCTTATTTGAAA[C/G]AGAAAAAGCATTTTA | 2074 |
rs181076176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478059 | AGAGCCTAGGATCAC[A/G]ACAGGCATATGGTTG | 2074 |
rs181092827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462087 | AAACCTTCATGAACA[A/G]ATCAGAAAACACTGA | 2074 |
rs181121867 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454068 | CTCTTCTTGTACTCC[C/T]ATTACATGCATACTT | 2074 |
rs181137363 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540831 | ACTCCTGCCCCATCT[A/G]ATTTTTCTGCATCAC | 2074 |
rs181143386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530663 | TACTTCCTAAATTAA[C/G]TGCCCCTAAATGATG | 2074 |
rs181146900 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514933 | TGGCAAATCTGAGCA[G/T]ATGAAATACCCTCAG | 2074 |
rs181147716 | snp | C/T | 0.000479089 | 0.0154698 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470945 | TCTTGTGCAATTGAT[C/T]ACTTTAAATTAAATG | 2074 |
rs181150197 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508174 | AAACATACTTCACTT[C/T]GCAATTTCTCCAAGA | 2074 |
rs181153073 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498077 | AAGGTGGTGTATCCA[C/T]TATGAAGGGGAACAC | 2074 |
rs181156051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477608 | CGATGCCCAGGTCTT[A/C]ACTTCTGTTCATGCA | 2074 |
rs181281177 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527488 | GAGACCAGCTTGGCT[A/T]ACATGGTGAAACCCT | 2074 |
rs181303124 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502003 | ATAAGGCATTTTTTT[G/T]TCAAAGAAAATATCA | 2074 |
rs181313599 | snp | A/G | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484077 | TGAGCCCAGGAGTTC[A/G]AGACCAGCCTACGCA | 2074 |
rs181327678 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458002 | CTTCATGGTAACAAC[A/G]GCTGGGTCTGCTGTG | 2074 |
rs181376120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512950 | TAAACTGCCTTTACT[C/T]GTGAAAGGTCACCTT | 2074 |
rs181396956 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474576 | TATAAAAAAGGAATT[C/T]GCCTTTTAAATATGG | 2074 |
rs181689302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502973 | AAACTGATGTGCAAT[C/T]AGTTTCCAGAATCAC | 2074 |
rs181693725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526726 | ATGAATTTCAACTAA[C/T]GAAAGAGGGATACTT | 2074 |
rs181694052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485319 | CGGAGAAAGGCAGCC[A/G]AATCCAAAGCTAGTA | 2074 |
rs181711005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512805 | TGAAACGAAGTTTTG[A/G]CTGTGTCTTGACTGA | 2074 |
rs181714169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466720 | TCAGAGTATGTACTA[A/G]TCTTACTAGTCCGAA | 2074 |
rs181838986 | snp | A/G | 8.30048e-05 | 0.0064417 | missense | ERCC6 | GRCh38.p7 | 10:49474230 | TTCTTAGGGCTATAA[A/G]TCCGGAGAAAATCTG | 2074 |
rs181877945 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513170 | AGGTACTGCTGTGAT[C/G]CCCATCTTACAGGTG | 2074 |
rs181878810 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536214 | GGATGAGGAAATGGA[C/G]GCCACAAGAGAGTGG | 2074 |
rs181891287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522109 | ACCACTAAAAAAAAA[C/T]TAATTTTCTATGTTG | 2074 |
rs181894299 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507465 | AAAAAAATTTAATGT[A/C]CTTTTTGTGCTTAAC | 2074 |
rs181902181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489015 | GTCTCGATCTTCTGA[C/T]CTCATGATCCGCCGG | 2074 |
rs181968598 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484735 | ACGGCGCAAGATCCT[A/G]ACTCAAAAGAGAAAA | 2074 |
rs182041939 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519206 | TCATACCTAAATATT[A/G]CACCTTCTACTCAAT | 2074 |
rs182071616 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533636 | ATGAGACCTTGTCTC[A/T]ACTAAAAATTTAAAA | 2074 |
rs182076171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517167 | AGTGGTAGTGGTTTT[C/G]CCTAGTGTTCCAAAA | 2074 |
rs182078746 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492870 | CTGTCTGAGATGATT[C/G/T]GTATTTTACTGGACA | 2074 |
rs182133004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499345 | ATCTGCTAACTTAAC[A/G]AAAGAGTAAGAAATA | 2074 |
rs182151909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463697 | TGATTAATTATGAAG[A/G]TGCGTCTTTCCTACA | 2074 |
rs182155585 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519676 | CCCAGAGGCAATTAT[C/T]TGCTGAGTGTGGGCC | 2074 |
rs182177140 | snp | C/G | 0.0103295 | 0.0711199 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457540 | GCAGACAGAAGATCT[C/G]GACACAGCTATCCAT | 2074 |
rs182240561 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502356 | TAAAAATCAAAACAC[A/G]ATGAAGTGTAGTACA | 2074 |
rs182262062 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466308 | TTTCTTGCCATAGTT[C/T]AGGTCAGAAATTGTA | 2074 |
rs182326641 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535850 | AGTTTCAGGCCAGGC[G/T]TGGTGGCTCACACCT | 2074 |
rs182334619 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481835 | GCGTCTCCTGCCCCA[C/T]CATCTTTCTCAGACC | 2074 |
rs182395696 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454607 | CTAGTTATAGCTAAT[C/T]CCTAGGACAGTGGGT | 2074 |
rs182397454 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540407 | GATAAAATATTAAGA[A/T]TAGAAAGGCAGTTGA | 2074 |
rs182413276 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479770 | GCTAGGCTGGGGAAC[A/G]GCCGGGCTGTGGCTC | 2074 |
rs182468745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500269 | CTAACCTTAGACATC[A/G]TATTGACCCAAAATA | 2074 |
rs182474210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480425 | AATAAATACCGGCAC[A/C]CAGACTATCTTCTTA | 2074 |
rs182482818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515878 | CACTGTTATCATTCC[A/G]TCTGCAGACAATATT | 2074 |
rs182529731 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485672 | ATGTGAGAAAAATAT[A/G]TTAAAATACATTTGC | 2074 |
rs182595892 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537217 | GGCATGGAGGCGCGC[A/G]CCTGTAATCCCAGCT | 2074 |
rs182610356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476082 | ACTGCACATCTACCA[C/T]GCGGGACTTCATGCA | 2074 |
rs182620289 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503584 | CAGCTGGTAGATGAT[A/C]TACATAGCTGGTGTT | 2074 |
rs182676622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525375 | GCTCAAGAGCTACAC[A/G]TGACTAATGGCTACT | 2074 |
rs182735288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508650 | TACACATATTAAAGA[C/G]AGAAAATATCATGGT | 2074 |
rs182753700 | snp | A/C | 1.65315e-05 | 0.00287498 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472330 | AAAATTCCCTGCTCA[A/C]GACTCTGGGAACGCA | 2074 |
rs182878899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521000 | CTGCACTGGATGAAC[C/T]TCCCCAACAGTCTCT | 2074 |
rs182884062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504484 | GACATTTATACAAAA[A/G]TGCAGACTCAACTTG | 2074 |
rs182887307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528690 | GAGAGCCCTATGTGA[A/G]CAACTACCACTTTTC | 2074 |
rs182891829 | snp | A/C | 2.56802e-05 | 0.00358322 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488215 | CTGCTGTTATTATGG[A/C]GGCTCAAGAGACCAA | 2074 |
rs182907329 | snp | C/T | 8.24042e-05 | 0.00641836 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516637 | ATAAGTTGGAGTACT[C/T]GACAATGAGTTCAAT | 2074 |
rs183001273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522734 | TTTATTAATTCCTTG[A/C]AGTAGTTAAGAAAAA | 2074 |
rs183014839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464493 | GCTGCAGAAATTTGC[A/G]TTACGTAACGAGGAG | 2074 |
rs183015636 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467692 | CAGCTCAGCCTCGCA[A/G]GTAGCTGGGACCACA | 2074 |
rs183022068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489525 | GAACCCTGGTCTTGT[A/T]AGCACAAAACCAATG | 2074 |
rs183072873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528874 | TACACACTGGGCAAA[C/T]CCCTAAACTACTCTG | 2074 |
rs183083814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495417 | GCCCCACAAAGATGT[C/T]GACTGTGTGAAGCAA | 2074 |
rs183171071 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468295 | CCAGCCACCCTGGCC[G/T]CCCCTGATGCTCAGC | 2074 |
rs183172300 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510457 | TCAAACCCTCACTCA[C/T]GCAGCACCACCATGC | 2074 |
rs183179468 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533056 | TTTATAATTAGAGCA[C/G]ACTGATTTCTCAAAA | 2074 |
rs183247492 | snp | G/T | | | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49539018 | CGCCGCCAGCCGCCT[G/T]GGAACCCAGCTCGAC | 2074 |
rs183326896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475138 | AGTCACTAGTCACAC[A/G]TGGCTACTGAGCACA | 2074 |
rs183339162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513761 | CTTCCCATCAGGTTC[C/G]TCCCTTGACATATGG | 2074 |
rs183460859 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523939 | CGGGGGGGTCTAATA[C/T]ATTAAGCTGGATCTA | 2074 |
rs183472492 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455095 | TTCCGTATGATAAAC[A/G]TCACAAAATAGATAT | 2074 |
rs183489509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473123 | CACATGGAATTACTG[G/T]GCTGTTCCCAATATA | 2074 |
rs183591888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513277 | TGCTATATACTGCCT[A/C]CTTAAGGAAAGTCAG | 2074 |
rs183599424 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518765 | GGGGCCCTGGCCACA[A/G]AGGCCCAGTGCTCAG | 2074 |
rs183608888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475724 | GGACAATGAGAATTA[A/G]AGCCAGGGACATTTG | 2074 |
rs183610676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502083 | GTCCAAATACTTACT[A/G]TCTGGTACCTATAGG | 2074 |
rs183684760 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535320 | AAAGTCTGGGTGACA[C/T]GTGGACACATCAGCA | 2074 |
rs183782033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520670 | GACATCACTAAGGAA[C/G]TGCACACTCTTCCCA | 2074 |
rs183799039 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487478 | GGCCTTAAAAACACA[C/T]GTACGGGTTCCCTCA | 2074 |
rs183820604 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494492 | TACGTAGAAAAACTG[A/G]TTGTGGCCATTGTCT | 2074 |
rs183937055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533905 | TTGGGAGGCTGAAGC[A/G]GGCAGATTACTTAAG | 2074 |
rs183971617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504146 | TACAGTAAAAAAATA[C/T]ATCTACAGTTTAAAA | 2074 |
rs183988801 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467917 | TTCATCTTGTTGGAT[A/G]TTGGGTATTTGTATA | 2074 |
rs184047796 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538396 | ATGCCAGAGACCACC[G/T]GGACAACTGTGCGGA | 2074 |
rs184076642 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465176 | CCTCTTGCATCAGCG[G/T]GACCTGGATGCGAGA | 2074 |
rs184125464 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484147 | TTAGCTGGATGTGGT[G/T]CCAAGCACCTGTAGT | 2074 |
rs184128830 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511410 | TAAAGTAAGTGTGTT[G/T]TTCATCTTCTTTTTT | 2074 |
rs184150520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518336 | CAAGCTGCGAGATCA[C/T]TCTCATGTGTCCCAC | 2074 |
rs184158421 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501889 | TGCTTGAGCCATGGA[A/G]GTTGAGGCTGCAATG | 2074 |
rs184175851 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484051 | TGGGAGGCTGAGGTG[A/G]GTGGATTGCTTGAGC | 2074 |
rs184231590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505746 | TGGCTATAATTTCAT[G/T]TGACAGTATCTGTTT | 2074 |
rs184265550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525874 | TACAGACAAGTTGTG[C/G]CTGTCTCTGAACGCT | 2074 |
rs184274103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465655 | GGTTGGGTCTTTCCT[A/G]TGCTGTTCTTGTACT | 2074 |
rs184278633 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492367 | GCTTCTCCCCAATAA[A/C/T]GTAACCTGCAAATTC | 2074 |
rs184298976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498828 | CTGGACTCCACATAA[G/T]TGTGATGATAATAGG | 2074 |
rs184302780 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539408 | TGCAGAGAAAGTCAG[C/T]TTGGGCAGGGAAGTT | 2074 |
rs184303020 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521337 | CTTGGCTGCACAGCC[C/T]GTACTAGGTAAGCAG | 2074 |
rs184689986 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460200 | TTTAGGAAATCAGCA[G/T]GTCCTTTTAGATTCA | 2074 |
rs184693795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530087 | CAGAGTGGAGACAAT[C/T]AGAGGAAGCAAGGGC | 2074 |
rs184697684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514210 | ATGATTCCTTCCCCA[C/T]CTTAATAGTGTGCAA | 2074 |
rs184709238 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526945 | ACCAGGGAGAGGCAG[C/T]AGAACAAGAAGAGGG | 2074 |
rs184733981 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457206 | ACTTTCTTCTAAGCC[A/C]AGTACTCAAGTTTAA | 2074 |
rs184757391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492639 | CGATCAAGGATTCAA[A/G]GAACAAAACACAACT | 2074 |
rs184761293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473897 | ACTCCCAAAGAAATC[A/G]GTAGACTGCCACCTC | 2074 |
rs184816494 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526203 | ACTGTCAGTTTTCCA[A/C]AGTGTTACGTTCCAA | 2074 |
rs184830255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512039 | TGCTATAACAGTTGG[C/T]AGATTACACAAAAAG | 2074 |
rs184852679 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468659 | CAACAAACACATACA[C/T]ACACATACATACATC | 2074 |
rs184853495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512823 | GTGTCTTGACTGAGA[C/T]CCAACATATGAGGTC | 2074 |
rs184856905 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534911 | ATCTACACCCGAGTG[G/T]CTATCCACTGGAGCA | 2074 |
rs184894995 | snp | C/G | | | missense | ERCC6 | GRCh38.p7 | 10:49530745 | TTCTGTCGTTTTACA[C/G]AATCTAGTTTCCTGT | 2074 |
rs184934227 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537821 | TCCGCCTTCCGGGTT[C/G]AAGCGATTCTCCTGC | 2074 |
rs184936332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520478 | AGAAGAGACAAAAAC[A/G]TATCTGGAAATGCAT | 2074 |
rs184951097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488814 | TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCCAGA | 2074 |
rs184989808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514753 | TAAAAATATATTCAG[A/G]CACCAAGCTGGGTAT | 2074 |
rs185019283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514942 | TGAGCAGATGAAATA[A/C]CCTCAGTTAGGAGTG | 2074 |
rs185087290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530519 | GTCTATGTATGTGTG[C/T]TTTTTTAAATGCAAT | 2074 |
rs185101323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497423 | TTATACAGTATTTTT[G/T]TCTCTTTTATAATGT | 2074 |
rs185116441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474817 | TATGGTCCATGCAGA[A/G]GGGCACAGAAGACAA | 2074 |
rs185142838 | snp | A/G | 0.000116738 | 0.00763906 | ERCC6 | 10 | allele_origin=G(germline)/A(germline) | 10:49461473 | CATCCTGGGCCACTC[A/G]GTTGGCTTCTGCCTC | 2074 |
rs185203927 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458082 | ACTTTTGGCTTTAAT[G/T]TGATTTTTTTTAATG | 2074 |
rs185363321 | snp | C/T | 9.94316e-05 | 0.00705024 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532492 | CATTACCTGAATATC[C/T]CTGTCATGTTTTACC | 2074 |
rs185428752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485409 | AGATTGTATGTGATA[C/T]ACATACCATTTAAAA | 2074 |
rs185438818 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466732 | CTAATCTTACTAGTC[C/G]GAAAGTCATCCATGC | 2074 |
rs185520092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521843 | CCATTAAAAAAGCTA[C/T]GGAAAGGGCTTGACG | 2074 |
rs185542294 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488919 | CTCCCGAGTAGCTGG[C/G]ACTACAAGGTGCCTG | 2074 |
rs185581540 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522535 | ATAAATTGTTTTACA[A/G]TCTTAACATTATTAA | 2074 |
rs185624511 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501690 | TTAGATGAGGTGGCT[C/T]ATGCCTGTAAATCCC | 2074 |
rs185639953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464906 | GGTTCTCATGGAGAA[A/T]CTCTCCTAGGGCAGT | 2074 |
rs185640854 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539755 | CAGCCCACGATGCAG[C/G]ATGGCTGTACCAGAC | 2074 |
rs185654374 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533448 | ACTCCTAGGCTGAAT[A/G]CCTATCCAGTAAATA | 2074 |
rs185662946 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540931 | GTGTGCTACAATTGG[C/T]TTCTACGGCCTAGCA | 2074 |
rs185673136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489196 | ACCATGAACATTTTT[C/G]ATAAAGTAGATGTGT | 2074 |
rs185682852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469472 | TATAGGAGAGTTCTT[C/T]GTATTATTCCAACTG | 2074 |
rs185683738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469932 | CACATCGATTTAAGA[A/G]TTGCACACCTCCCAT | 2074 |
rs185744003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517679 | ACCTCAGCCTCCTGG[A/G]TAGCTGGGACTACAG | 2074 |
rs185755164 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540656 | TAAGGGCCGAATTGT[A/G]TCCCCTCCCCAAAAT | 2074 |
rs185761464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522139 | GTAAACTCTATGACT[C/T]TATTCTAATCATCCA | 2074 |
rs185763349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507645 | AACAATCGTTCTTGA[C/G]AGGGGGCAATTCTGT | 2074 |
rs185835475 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486287 | TTTGAGTATCACCAT[C/G]AGACCTCCTTTCAAC | 2074 |
rs185835695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513121 | AGTGCCTGATGTATG[A/C]CAAATATCTTATACA | 2074 |
rs185903947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536733 | CTAACAATCTCCAGG[A/G]CTGAACAATCTCCTC | 2074 |
rs185905996 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519904 | CACTCTGCACCTGCT[A/G]CCTCAGACTCCCCAC | 2074 |
rs185912478 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503271 | GACAACTAGATTCTG[C/T]GTGGCCCAGGAAAGG | 2074 |
rs185957393 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503765 | TTTTGAAAAGCATAT[A/G]AAAATTACTCTTTAG | 2074 |
rs185964855 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527717 | GCTTCAATTAATTCT[A/T]CATAACAATTCTCAT | 2074 |
rs185983078 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522736 | TATTAATTCCTTGCA[G/T]TAGTTAAGAAAAAGT | 2074 |
rs185998785 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489706 | CTGTTTCAGAACATA[A/G]GCAATTTATCATTAT | 2074 |
rs186126620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508696 | ATACAGAGCTCAGGC[A/G]AAGAGATTCTTCTGT | 2074 |
rs186262133 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457703 | GAAATTTCAGGAATA[C/T]GATGAATTTCGGAAA | 2074 |
rs186324912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492923 | CACAGACTGTTAGAA[A/C]AATAAGACCTATATT | 2074 |
rs186389164 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454842 | GCAAAGTTAGATAAA[C/G/T]GGACCAATTTAACAG | 2074 |
rs186418414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478320 | GACACACTTGTGCTT[C/T]AGGAATGCTTCGTTA | 2074 |
rs186482480 | snp | A/G | 0.000132646 | 0.00814281 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459239 | ATGATGCCATCCTAT[A/G]AAAAGAAGACCACTA | 2074 |
rs186494062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471408 | ACACCTTTTCACATG[C/T]CATCATGTGACTCAT | 2074 |
rs186519141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513215 | ACCTCAGAGCTACTC[A/G]GCTAGGCTCTGGCAC | 2074 |
rs186526364 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494222 | TTTAACCTCTGGGAA[C/T]GTCAGTTTTTCATTT | 2074 |
rs186528006 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495607 | CCCCAAAGCACCACA[C/T]GCCATCCTCCCCTAC | 2074 |
rs186532065 | snp | C/T | 0.000371816 | 0.0136297 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475386 | AATTCCAAGTGTAGT[C/T]TGCATTCCCTTTCCT | 2074 |
rs186541840 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476084 | TGCACATCTACCATG[C/T]GGGACTTCATGCAAG | 2074 |
rs186596825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528198 | ATGTGTACCAGCAGC[C/T]TCCTATGAACTGAGT | 2074 |
rs186607931 | snp | C/T | 3.3195e-05 | 0.00407387 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516320 | ATCAAAGCTGAAATA[C/T]GTTTCATTTGGAACA | 2074 |
rs186614117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513831 | GCCAAACCATATCAA[C/T]ACTATTGTTATTCTC | 2074 |
rs186637963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479832 | TGATCTTCTGTTTCA[C/T]TCCCAACTGGCTCCC | 2074 |
rs186657475 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533716 | GCTGAGGCAGGAGGA[A/T]CACTTGAGCCTGGGA | 2074 |
rs186668269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517177 | GTTTTGCCTAGTGTT[C/T]CAAAAATGGAACATG | 2074 |
rs186678583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501419 | TCATAGCTATTAAGA[C/T]TTTAAATAAGGAATA | 2074 |
rs186699839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489468 | GGAAGGCAAGTGATT[C/T]GCCCAAGCTTGCAAA | 2074 |
rs186721314 | snp | G/T | | | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454159 | TCTCTCTGTTCTTTG[G/T]AAAGCATATCTCTCT | 2074 |
rs186839348 | snp | C/T | 3.29495e-05 | 0.00405877 | missense | ERCC6 | GRCh38.p7 | 10:49532781 | TCGGAGCTGCTGATG[C/T]GCACCCCACAGCAGA | 2074 |
rs186853896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499571 | GGGCACACCCCTCTA[A/G]CAACTACCTTGCTCT | 2074 |
rs186865820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463699 | ATTAATTATGAAGAT[A/G]CGTCTTTCCTACACT | 2074 |
rs187101379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500308 | GGCTCATCTGCAAAA[G/T]GAAGCATCAATGCCT | 2074 |
rs187118196 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464172 | GTCCAAACTGAGGTG[C/G]TCTCAGACGGAGATG | 2074 |
rs187165709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463654 | CTCCCACAATTCCCA[A/C]GTGACATGGGAGGAA | 2074 |
rs187180008 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490414 | GGCTAGAGTGCAGTG[A/G]CACAGTCCAGGCTCA | 2074 |
rs187185661 | snp | A/C | 4.9436e-05 | 0.00497148 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516645 | GAGTACTTGACAATG[A/C]GTTCAATGACCTCGT | 2074 |
rs187332822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502410 | AAGAAGGACAAATTC[C/T]GAAAATATGTGGTAT | 2074 |
rs187362525 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466367 | AAGTAACTCAGTACG[C/T]TGTGAATGAAGGTCT | 2074 |
rs187368553 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455252 | AAAATTTCATCCAAG[A/T]ATATAAAAGACTTTA | 2074 |
rs187400921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509553 | TGCTGGAATATCTCA[A/G]TTTAAAAATTCTGTC | 2074 |
rs187405520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490306 | GAAGAATGATAGATG[C/T]GCTTAATTGAGAAAT | 2074 |
rs187410426 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472717 | GGAATGAATGCTATG[A/G]ATAAACTGCTGAAGA | 2074 |
rs187520702 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521239 | GAGGTAACAAGGACT[A/G]GGGACAAGCGACCTG | 2074 |
rs187520848 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505521 | CAATATTGATTTTAA[C/T]ATGCAACTCTTCCTA | 2074 |
rs187536268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468522 | GTTTCACATGGAAGG[A/G]TAAATGTTAATCTGC | 2074 |
rs187592547 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49539038 | CCCAGCTCGACGGGC[A/C]GTGGCGCCTGCGCCC | 2074 |
rs187596668 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519603 | CCTACTGAAGAGTCC[A/G]TTTCTGAACTCCCCA | 2074 |
rs187615677 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484824 | GAAAATATTCCCTTC[A/C]GAGGAAAAAGACTAC | 2074 |
rs187628326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464503 | TTTGCATTACGTAAC[A/G]AGGAGCCAAATGTTA | 2074 |
rs187650948 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458710 | CATGCAAACAAACAT[C/T]AAGTGCAGCCAACTT | 2074 |
rs187671753 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525898 | GAACGCTACGTAAGT[A/G]GAAATGTTTGTGCCC | 2074 |
rs187758327 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467726 | GTATGCTACCACACC[C/G]GGCTATTTTTTTTTT | 2074 |
rs187797961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529500 | TCAATTTCACATGCT[C/T]CCACAAGAGACCAGA | 2074 |
rs187895672 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482248 | CATCCCTGAACAGTC[A/C]AATCCTCCTAGTGTC | 2074 |
rs187915828 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530272 | CCAACTTATCATGGT[A/C]TGACTTGCAATTTTT | 2074 |
rs187917425 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514565 | ATGTTGCAAGGATCA[C/T]TGTACACAGAGCAGT | 2074 |
rs187925706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497200 | CCCCAAGGAGAGTGG[G/T]ACTCTGCCTGGCCCC | 2074 |
rs187999276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468156 | CCTTTTCACTGACCT[G/T]AAGTAGTTTTCTTGC | 2074 |
rs188156428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510941 | AAATGGTTAAGGTTC[A/G]CTACAAAAAAATGAC | 2074 |
rs188165138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492524 | AAAAAAGGAAGAATA[C/T]AACGTATCTATGCTA | 2074 |
rs188171129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473739 | AGAACTGTTAAAAGA[A/G]TATTTTTGGTATTTC | 2074 |
rs188189367 | snp | A/G | 1.64838e-05 | 0.00287083 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515423 | CTTATGACATTCAGC[A/G]CATCGCGTTTGCTTT | 2074 |
rs188201328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498910 | CATTTAAGGAAAGAA[A/G]GAGTCCTAGAAACCA | 2074 |
rs188207506 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539577 | CCTGCTTACATGTGT[A/G]CATTGCCTTAAGTCC | 2074 |
rs188214518 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478023 | TGAGAACAAAACTTG[C/T]TTTGTTCACTGCTGT | 2074 |
rs188227731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482951 | CCTCTGCAAATTATT[C/T]ACACATTTACTCATC | 2074 |
rs188228522 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457035 | TATGTTTCAGACACT[A/G]TAAGTATGATACCCA | 2074 |
rs188246668 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511637 | TGCCATATTGGCCAA[A/G]CTGGTCTCAGACTAC | 2074 |
rs188254765 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462775 | TAAAACTTAAGATAT[C/G]CTTTCTCACCTATCA | 2074 |
rs188282803 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49532170 | TAGAAAGAAGCTACC[A/G]CACAGAGAAAAATGT | 2074 |
rs188351461 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535625 | TAAGAAAAAAGGATG[C/T]CAATTCAACCAAAAA | 2074 |
rs188392002 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528722 | AGGAGTAAAGGGGCC[A/G]TGAATATTCCCAGCA | 2074 |
rs188408328 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495107 | TTTGAGACCAATCCC[C/T]TTAGCTAAGCTCTTG | 2074 |
rs188439346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525587 | ATACCAAAAGACCTA[A/C]GGCTTAATAGGAAGG | 2074 |
rs188449665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491186 | ACATTTCCAATGTGT[C/T]GTCACCACAAATAAG | 2074 |
rs188521990 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465004 | ATGAGAAGAGGGCCA[C/T]GGTCCTCCAGACCCC | 2074 |
rs188527662 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534993 | GGACAAGAGGTCACA[C/T]GAGCATCGAGCGAAC | 2074 |
rs188580072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534399 | AACTAGTCACACACA[A/G]GTGCAAGAATGTTTA | 2074 |
rs188603024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501743 | GGAGGATCATTTAAG[C/T]CCAGGAGTTCAAGAC | 2074 |
rs188688471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513529 | AGACTGGGTAATTTA[C/T]AAGGAAAGAGGTTTA | 2074 |
rs188701457 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475835 | TGAAAGTTATGAATC[C/T]TCATGATCCTCTCCA | 2074 |
rs188824461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518635 | TCCAAATCCACAAGA[C/T]TCTCTTCATAACAGT | 2074 |
rs188838838 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501923 | CATGATTGCACCACC[A/G]GATTCCAAACTGGGC | 2074 |
rs188842893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484062 | GGTGGGTGGATTGCT[C/T]GAGCCCAGGAGTTCG | 2074 |
rs188848465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526657 | CTGAGTATTTTGCTT[C/T]CTATTAAGCCTTAGG | 2074 |
rs188853102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465411 | TGCCTGGTCTTGGAT[A/G]AGACTCTGGACTGTG | 2074 |
rs188856446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512394 | AAGGGGCATGTTGCA[C/T]GGTTTGTCCCCTAGA | 2074 |
rs188867799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492673 | AAGCAACAATACTTG[C/T]GAAATTCTCAAGATG | 2074 |
rs188945685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538553 | ACAGGCGGCCTGCCT[C/T]ATCCGCCCACACTCT | 2074 |
rs188957429 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476798 | CCAACCACTCCATGC[A/G]ATCGTGCTCTGTGAC | 2074 |
rs188967511 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504356 | TAATTTTTAAAAAAC[A/G]AATATTATTTATATT | 2074 |
rs188994444 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522264 | ATGAGTAACAAAATA[C/T]AGAGAGACTGGCAGT | 2074 |
rs188996507 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540715 | CCCACCCCCACCCCG[C/G]GACCTCAGAATGTGA | 2074 |
rs189009933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508055 | AATGAGAGAGTCCTC[A/G]GTATCAAAACTATGA | 2074 |
rs189016139 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489235 | TCTAGACTACATACT[C/G]AGTCAATCAGCAATG | 2074 |
rs189096558 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521581 | TGTATACCACTGACC[A/G]TAGAACCGACAGAAC | 2074 |
rs189113095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488815 | TTGAGACAGAGTCTC[C/G]CTCTGTCGCCCAGAC | 2074 |
rs189163770 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460257 | GTGCAACACAAATAT[C/G]AGGTGTCATTACACC | 2074 |
rs189173409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465957 | GAAGGGGTGGGGACA[A/G]GGTGGGGGATGACAC | 2074 |
rs189233856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520918 | GAGTTTAGGGGCAAA[C/T]GCGTAACATTGTTAA | 2074 |
rs189254749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487851 | TGATTAACAAGAATT[A/T]AAAAGATGCTTATGT | 2074 |
rs189257379 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502131 | TCATTTTGGACTTCA[A/G]CTCATTTAACTGGTT | 2074 |
rs189383381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506930 | GGAATAAAACAATAA[C/T]ACAGAGAAATGCTTT | 2074 |
rs189405028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469075 | TTACAATAGAATGTT[A/C]ATCACCATTTGGCAA | 2074 |
rs189413944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512904 | TTTTGGATTTTCGGA[C/T]TAGGGATGGTCAACC | 2074 |
rs189478040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488990 | GGGGTTTCACCATGT[A/G]GCCAGGATGGTCTCG | 2074 |
rs189488158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469566 | AAATTAACCATGCTA[A/C]ATAAAAGTCTTTCTG | 2074 |
rs189527812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519169 | GGGCAGCTATGTGTT[G/T]ATTTTTGGCACCACC | 2074 |
rs189549516 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484519 | CTGAGGGAGGAGAAT[C/T]GCTTGAGGCCAGGAG | 2074 |
rs189676751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533585 | GCCAGGGAAACACAG[A/C]GAGCTCAGGACTTCG | 2074 |
rs189681756 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527083 | CAAGGAACAGAAGTG[A/T]CAGCTGCTGTGGACA | 2074 |
rs189696611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481351 | TTTTTTAAAAAAAAG[A/G]ATGGTATAACAGGAG | 2074 |
rs189706198 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464344 | CTAAGCAGCAAAGCA[G/T]TCAACAGGTGACATG | 2074 |
rs189747333 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474378 | TTTCTTCTCTAGTCA[C/T]AGCATTATCATGAGC | 2074 |
rs189862487 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458192 | GCTTTCCACAAATAC[A/G]TGTCTTATCATTTAT | 2074 |
rs189910526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513136 | CCAAATATCTTATAC[A/C]TATCATCACCCATGA | 2074 |
rs189911662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536856 | AGTAGCTGAAGCAAC[C/T]GACTTCAGGGTCCAA | 2074 |
rs189913019 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493550 | CAAATATTATTTAAC[A/T]AAAATACTCTTTTCC | 2074 |
rs189922841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474828 | CAGAAGGGCACAGAA[A/G]ACAAGGGGTGAGTGC | 2074 |
rs189928289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519930 | CCCACGCTGAGCCCA[A/G]GCCCCTACCCTCTGA | 2074 |
rs189930147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503334 | ACAAATCTAATCTTC[C/G]ACGGCTTTCAAACAG | 2074 |
rs189942338 | snp | A/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457536 | ATGAGCAGACAGAAG[A/T]TCTGGACACAGCTAT | 2074 |
rs189943789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485571 | AAAAGCTGGATTGAG[A/G]TTAAGGGAAAATAAA | 2074 |
rs189950035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467066 | GATTACAGGCGTGAG[C/T]CAAGCCCCACCTGTC | 2074 |
rs189979670 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457915 | GGAATGCAAAGGCAG[A/G]CGCAAGACGAAGGCA | 2074 |
rs189985047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519636 | ATGTTTCCCTGATCG[A/G]GGTGGGCATGGGTCG | 2074 |
rs189990664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528038 | CTGCCAAATACGCTC[C/T]TTAAAGACACGTGAG | 2074 |
rs190068019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530620 | AATTATAAGTATTTG[C/T]TTCACATCTTATAAG | 2074 |
rs190083844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497969 | TGATATCCAAGACTT[G/T]AAAAAATTAACTGAG | 2074 |
rs190147988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502909 | GAACTGGCTACACTA[A/G]AATAATCTCAACTTT | 2074 |
rs190213675 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540336 | GAGCCACCACGCCCG[G/T]CTTGTAACTTGCTTT | 2074 |
rs190224481 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536170 | AAACCAGACTGTAGT[A/G]GTTGAAATGTAGTTG | 2074 |
rs190244863 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477161 | TCTGTCTCAACTTCT[A/T]CTTAAAAACAATCAG | 2074 |
rs190321205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514770 | ACCAAGCTGGGTATT[G/T]AATATAGTTTGCATT | 2074 |
rs190420677 | snp | C/G/T | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466612 | GCAAAACTCATGTCC[C/G/T]TTTGTAATCCCACCG | 2074 |
rs190476306 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521930 | TGCCAGTGAAAGGCC[A/G]ATGGCTCTCAAGCTG | 2074 |
rs190539745 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507450 | AGTGATACTTTTTAT[A/T]AAAAAATTTAATGTC | 2074 |
rs190611014 | snp | A/C | 6.60404e-05 | 0.00574594 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528406 | AGAGAAACTGCTCCT[A/C]GCATCCTCACCTGCA | 2074 |
rs190612981 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513238 | TCTGGCACTCACTCC[A/G]TGGCCCGTGGTGTCT | 2074 |
rs190766091 | snp | G/T | 0.00199481 | 0.0315187 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454208 | GCTGACAATTTCTTC[G/T]GCCAGTTCAAATCTA | 2074 |
rs190769997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522733 | TTTTATTAATTCCTT[A/G]CAGTAGTTAAGAAAA | 2074 |
rs190780411 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489509 | AGCAGATCCAAGATT[C/T]GAACCCTGGTCTTGT | 2074 |
rs190840145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467798 | GGTTTTGAACTCCTA[A/G]GCTCAAGCAATCAAC | 2074 |
rs190843349 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508891 | CTTCCTCATCCCAGA[C/T]GCTGCCAAGAGACTT | 2074 |
rs190849265 | snp | C/G/T | 0.00026499 | 0.0115077 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532495 | TACCTGAATATCCCT[C/G/T]TCATGTTTTACCACC | 2074 |
rs190855816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489765 | CCTTAATCATTAAAT[A/G]AACTTTACAAGACAG | 2074 |
rs190863815 | snp | A/C | 0.00334131 | 0.0407368 | missense | ERCC6 | GRCh38.p7 | 10:49472425 | TCAGGAGCCTGTACA[A/C]AGTCACTTGCTTCTT | 2074 |
rs190896169 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454945 | AATAATAAACTATTT[G/T]TTAAAGGTGCTAGGG | 2074 |
rs190909624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537958 | AACTCCTGACCTCGG[C/G]TGATCCACCCACCTC | 2074 |
rs190918638 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503889 | GGTGTACATTGGCAT[C/T]GCCACACTAACCCAA | 2074 |
rs190939831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471672 | CTAAAGCATGAATCT[A/G]TAAAAGGAAGCTCTC | 2074 |
rs190996793 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49541028 | CAGCTTAAACAACAG[A/G]CATTTGTTTCTCATA | 2074 |
rs190997340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475858 | CCTCTCCACAAGATA[C/T]ATAATTCTGGTCATA | 2074 |
rs191016723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508593 | CATTATTGCCTGCAA[A/G]TATTTGTATCATTGT | 2074 |
rs191076765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513634 | TTCACAAGGCGGCAG[C/G]AGGAAGTGAGTGCAA | 2074 |
rs191078520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486953 | CACTACTTTACAGAT[A/C]AAACCTAGTAATATA | 2074 |
rs191158266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520494 | TATCTGGAAATGCAT[C/T]TTCTCACTCAGGATG | 2074 |
rs191235578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495241 | AAGTCAAAACTAACC[A/G]TGGCAACCTCTTCAA | 2074 |
rs191403740 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514049 | TTCTCACAGTGCCAG[C/T]GAAGGGTCCTCTAAC | 2074 |
rs191406465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496804 | CAAGAGCGAGACTCT[A/G]TCTCAGAACAAACAA | 2074 |
rs191416909 | snp | C/T | 5.03216e-05 | 0.0050158 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476191 | TCCACAATTCATTTC[C/T]CCAGCTTCTATTTTT | 2074 |
rs191491251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485079 | GTGGAGTGGTGCAGT[C/T]GTGGACAAAGAGGAA | 2074 |
rs191563938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494480 | TAGACATAGGTATAC[A/G]TAGAAAAACTGGTTG | 2074 |
rs191636031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500263 | TAGAAGCTAACCTTA[C/G]ACATCGTATTGACCC | 2074 |
rs191665343 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539242 | AGCTGTCTCCGCTGC[C/T]GGTCAGCTGGGTGGC | 2074 |
rs191668529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521280 | CCCTGAAGGGGAAAG[A/G]TTCACATGAAATGTT | 2074 |
rs191681758 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505704 | TTTTAGTCAACTTAT[C/T]ATCATCCAATTTTAA | 2074 |
rs191684401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488741 | GGCCCTTTTAAAGAA[C/T]ATGTTGATGGGAGTT | 2074 |
rs191731244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533024 | GTTATATAGGATTCA[C/T]TGTAGTTCTTAAATA | 2074 |
rs191793152 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535279 | TTTGCAGCATGCAGT[A/C]AGAAATGCAAATCTG | 2074 |
rs191807800 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518742 | ACCCTCCCAAGCCAG[G/T]GTTCAATGGGGCCCT | 2074 |
rs191829571 | snp | C/T | 0.000346292 | 0.0131539 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478497 | GCAGAGAAGGGAACA[C/T]TACTATATATGTTTA | 2074 |
rs191843476 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475405 | ATTCCCTTTCCTGGA[G/T]AGTGTGATCTAGACC | 2074 |
rs191940241 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480340 | TGCCCACCCCTACTG[A/G/T]ACTGGAAATACCTTC | 2074 |
rs192031942 | snp | C/G | 9.89903e-05 | 0.00703458 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516607 | AGCCAAGATGTACAC[C/G]TTTACTGCAAGCATA | 2074 |
rs192092102 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523185 | TTTAAAAGTAATAAG[A/G]TTCCTTTTTCCCTTT | 2074 |
rs192123314 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499219 | CAACAACAACACGAT[C/G]TTTAGCATTTAAAAA | 2074 |
rs192124794 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504413 | CTGAATCCTAAATAC[G/T]TTTAGTAAGCAAAGT | 2074 |
rs192139039 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468254 | TGTGCAGAGCTGTCT[C/T]CGCTATCGTCTCTTG | 2074 |
rs192242583 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456578 | AGCTGTGGAACAGGT[A/G]CAAGATGGTGTGGGG | 2074 |
rs192276806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491955 | CTAGACAACAATCTA[C/T]ACTGCTATTATCTTC | 2074 |
rs192280143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525139 | TGAGGAAGCAAGCTC[C/T]GAAGTTCTCACGTCA | 2074 |
rs192282270 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484001 | GATAGAAAAAAAGCC[A/G]GGTACAGTGGCTCAC | 2074 |
rs192290938 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465005 | TGAGAAGAGGGCCAC[A/G]GTCCTCCAGACCCCA | 2074 |
rs192296400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490600 | CCTCGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 2074 |
rs192300032 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457119 | CAATTTCCTTATAGG[A/C]TAATGATTATAAAAA | 2074 |
rs192371768 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511985 | ACTAAATGAAATTAT[A/G]TATGTACATTATACT | 2074 |
rs192375778 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533904 | TTTGGGAGGCTGAAG[C/T]GGGCAGATTACTTAA | 2074 |
rs192375996 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492560 | AGGAGCACAGATAAA[A/G]CTCTTTTTTGATACT | 2074 |
rs192386303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473890 | GATCTAAACTCCCAA[A/G]GAAATCGGTAGACTG | 2074 |
rs192422121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506967 | ACAATAAAAAAAAAA[A/C]TCATAGGAAGCGAGT | 2074 |
rs192442654 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469442 | CTGAAAAATGTTAAT[A/G]ACTTAGATAAAGGAT | 2074 |
rs192457757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463655 | TCCCACAATTCCCAC[A/G]TGACATGGGAGGAAC | 2074 |
rs192503962 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539685 | GAAGAAAGAAGATGT[C/T]CACACAGAGGTTCAG | 2074 |
rs192523259 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530318 | TTTATCAGGGCATAA[C/T]CCCATTATAAACTGA | 2074 |
rs192681212 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511299 | GTCTAGACTTAAACT[A/G]TATTTACATTACTAG | 2074 |
rs192697328 | snp | A/G | 0.000297619 | 0.0121951 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473052 | AAGACACACAACACT[A/G]AGCACACACACTTAA | 2074 |
rs192729223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525828 | CAGCCTCTACGCCCC[C/G]CAAGATAATGATGGA | 2074 |
rs192770492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488823 | GAGTCTCGCTCTGTC[A/G]CCCAGACTGGAGTGC | 2074 |
rs192814563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521814 | AGCAGGATCCAAAGG[A/G]CGACTGCCCAGTTCC | 2074 |
rs192815443 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468550 | TGCCTTTGCTGGAAG[C/G]CAAATTCATGGTTTT | 2074 |
rs192870759 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460750 | ACATGGTGAAATCCC[A/G]TCTCTACTAAAAATA | 2074 |
rs192879899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520944 | GTTAATTTGGATAAG[A/G]GTCATATTAATATAT | 2074 |
rs192961728 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501835 | AGTGGTGGCACGTGC[C/T]TGTAGTCCTAGCTAC | 2074 |
rs192976944 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49472772 | AGGGTGTCTTCTTTC[A/T]CGTTGAAGAACAGGA | 2074 |
rs193000115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534652 | TCCACATACTCAGGA[C/T]CTGCTGCTTTAAGGA | 2074 |
rs193004683 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482609 | CACATTCTGAATGAC[A/T]TGGCTACAAATTATA | 2074 |
rs193043670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517220 | CCCATAACTAATGCA[A/G]TAATAATACTTTCTG | 2074 |
rs193087857 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477139 | CACCACCCAAGCCAC[A/C]CGCAACTCTGTCTCA | 2074 |
rs193111084 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497368 | TTTACAACAAACTCA[C/T]ATTCAAATAAGCATA | 2074 |
rs193165336 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455309 | ATCAGAAACATTATA[C/T]TAATTATAAAGAGGT | 2074 |
rs193182084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517890 | GAGATGTTAAGAACA[A/T]TCTTAAAATAATTGT | 2074 |
rs193207336 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464744 | TGGCTTCAGATGGTG[C/T]AAGCCCCAAGCCTTG | 2074 |
rs193227613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501493 | AAAAACAGAAGTTGA[G/T]ATTTTTCTTTCTCCA | 2074 |
rs193264187 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49514593 | AGTTTAAATCTACAC[C/T]GTCTGTAAGGAAAAA | 2074 |
rs193265322 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538689 | CTGACCCTGCGCGCA[A/G]GGGGCCTTATACAAA | 2074 |
rs199514935 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507958 | ACACATATCTGAATT[A/C]TTGATATATATACAC | 2074 |
rs199528821 | snp | A/G/T | 0.000659006 | 0.0181405 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473433 | GTCCTTTCCCTCCAC[A/G/T]TACAGCAGCACCACT | 2074 |
rs199560976 | snp | C/G | 0.000148332 | 0.0086107 | intron-variant, stop-gained | ERCC6, PGBD3 | GRCh38.p7 | 10:49516632 | AGCATATAAGTTGGA[C/G]TACTTGACAATGAGT | 2074 |
rs199567314 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488642 | TAATGTGGCCTCTTT[C/T]TTTTTTTTTTTTTTT | 2074 |
rs199581226 | snp | C/T | 0.00199806 | 0.0315443 | missense | ERCC6 | GRCh38.p7 | 10:49472379 | GTGTGCACTGACCGG[C/T]GGTAGATCTTTTCTT | 2074 |
rs199656826 | snp | C/T | 0.00199792 | 0.0315431 | missense | ERCC6 | GRCh38.p7 | 10:49532814 | TGGACAGCCCGTCAC[C/T]CACAGAACGAAAGGA | 2074 |
rs199661164 | snp | A/G | 1.66479e-05 | 0.00288508 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516176 | TGGGTTTTTACCCTG[A/G]TACGGCTGAAACCAG | 2074 |
rs199686337 | snp | A/G | 0.00199804 | 0.031544 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461516 | ATCTGGGCTGGCTCC[A/G]TCCATGATGGCATCG | 2074 |
rs199692102 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511455 | TTTGAGACAAAGTCT[C/T]ACTCTGTCACGTCAG | 2074 |
rs199692498 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484306 | AGAAAAAAAAAAAAA[C/T]AAAATGTTAGAAAAC | 2074 |
rs199695627 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537506 | ATATATATATATACA[C/T]ATACACACACACACA | 2074 |
rs199697610 | in-del | -/TT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511428 | CATCTTCTTTTTTAC[-/TT]TTTTTTTTTTTTTGA | 2074 |
rs199723819 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515761 | TATACACTTTGATCA[C/T]GTTTGGCTGCTGAAC | 2074 |
rs199726600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460479 | AAGCATCACAGTAGA[C/T]TAAATGTTTGCTTTT | 2074 |
rs199774616 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507962 | ATATCTGAATTCTTG[A/C]TATATATACACTTTC | 2074 |
rs199779724 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489739 | TCTTCCAATAAATTG[-/A]AAAAAAAAATCCTTA | 2074 |
rs199823585 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501796 | CCTCATCTCTACAAG[-/A]AAAAAAAAAAAAATT | 2074 |
rs199833250 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538125 | ATGGCCTAAGTCTTG[C/T]AGAGTATCTTCTAAG | 2074 |
rs199844680 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499987 | ACTTCATTCAAAAAC[A/G]AGAGAGAGAGCAAGC | 2074 |
rs199870074 | snp | A/G | 0.000198075 | 0.0099498 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482870 | GGTGCGAAACTATTT[A/G]AGGAAAGGAAGCACC | 2074 |
rs199899782 | snp | A/G | 0.000658946 | 0.0181394 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524468 | TCCTCTTTTTTGGAC[A/G]GAACTCTGGCTTTCT | 2074 |
rs199921831 | snp | A/T | 0.000247156 | 0.0111138 | missense | ERCC6 | GRCh38.p7 | 10:49482779 | CTAACTTTCCCGGGA[A/T]GATGAAGTCAAAGAG | 2074 |
rs199955995 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468993 | TCATGGAAAAAAAAA[-/G]AATCCATTAGTCCAC | 2074 |
rs200038908 | snp | A/T | 1.6495e-05 | 0.0028718 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478502 | GAAGGGAACATTACT[A/T]TATATGTTTAAGGAA | 2074 |
rs200055797 | in-del | -/G | 0.0123036 | 0.0774623 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540347 | CCCGGCTTGTAACTT[-/G]CTTTTTTTTTTTTTT | 2074 |
rs200079929 | snp | A/G | 0.000116187 | 0.00762104 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474228 | TTTTCTTAGGGCTAT[A/G]AGTCCGGAGAAAATC | 2074 |
rs200091337 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526147 | TATATATATATATAT[A/T]TATATATATATATAT | 2074 |
rs200093886 | snp | C/T | 6.59098e-05 | 0.00574026 | missense | ERCC6 | GRCh38.p7 | 10:49470769 | GATGATGTGGCATCA[C/T]TTACAGATATGTTAG | 2074 |
rs200100617 | snp | A/C/T | 0.000182468 | 0.00955009 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500712 | CTATGACAACAAACA[A/C/T]CAACAAGAAAAGAGA | 2074 |
rs200121511 | snp | A/C | 0.000661244 | 0.018171 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516509 | ATCTGTTCTTTGTTC[A/C]CAAAACATACGCCTT | 2074 |
rs200147578 | snp | C/T | 0.000336554 | 0.0129678 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524798 | AGAACAATAGCAATG[C/T]GTTTCGCACTAGCAT | 2074 |
rs200156549 | in-del | -/TA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537487 | ATATATATATATATA[-/TA]CACATACACACACAC | 2074 |
rs200160266 | snp | C/G | 0.000148941 | 0.00862835 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473996 | GTCATAAAGAACCAG[C/G]CTGTTTCCCGTCTGA | 2074 |
rs200176726 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471840 | TCTGTGGTGGGGGAG[C/T]GGGAGAAGCTGGCAA | 2074 |
rs200235830 | snp | G/T | 0.00199792 | 0.0315431 | missense | ERCC6 | GRCh38.p7 | 10:49493191 | ACGTGTGAAATTCCT[G/T]CACCCACTGATGCAT | 2074 |
rs200239727 | snp | A/G | 0.000908828 | 0.0212976 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470934 | ATATTGTATCATCTT[A/G]TGCAATTGATTACTT | 2074 |
rs200254508 | snp | A/G | 8.23635e-05 | 0.00641677 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49458980 | CTGGCCATCAGTGTG[A/G]GCCTGGAAAGCGATG | 2074 |
rs200272551 | snp | A/G | 0.000461764 | 0.0151878 | missense | ERCC6 | GRCh38.p7 | 10:49482863 | GATGAGGGGTGCGAA[A/G]CTATTTGAGGAAAGG | 2074 |
rs200274791 | snp | C/T | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516718 | CGGTGAAGAAATCGT[C/T]TGGTGGTGCTGTAAC | 2074 |
rs200291655 | snp | A/G | 1.64838e-05 | 0.00287083 | missense | ERCC6 | GRCh38.p7 | 10:49472409 | TCAATGGTGCCCGCA[A/G]TCAGGAGCCTGTACA | 2074 |
rs200302619 | snp | A/G | 0.000264817 | 0.0115038 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516256 | GAATGGGCTTTCCCC[A/G]AATAAATTGTTTGCA | 2074 |
rs200326979 | snp | C/T | | | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515507 | CTTCTGAGGTCTTCC[C/T]TTTTGGCCAGGTTCT | 2074 |
rs200360361 | snp | G/T | 0.00123537 | 0.0248226 | missense | ERCC6 | GRCh38.p7 | 10:49470483 | TTGAGCCTGGCTGGG[G/T]CTTTCTCTTTTGTAA | 2074 |
rs200370370 | snp | C/T | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515539 | GAGGATGACCATGGG[C/T]CTCCAGATAATGGCA | 2074 |
rs200424254 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516830 | TGGAGGTTGCTGCAC[A/G]GTAAACGTAGATGGA | 2074 |
rs200424879 | snp | A/G | 4.94181e-05 | 0.00497057 | missense | ERCC6 | GRCh38.p7 | 10:49458903 | AATAGTTCTCGGAAG[A/G]CACAAGACTGTGATG | 2074 |
rs200428567 | snp | A/G/T | 4.96589e-05 | 0.00498271 | missense, synonymous-codon | ERCC6 | GRCh38.p7 | 10:49460418 | AGGATGCTGCACAGA[A/G/T]AAGTTAGAATTCCTT | 2074 |
rs200431100 | snp | C/T | 6.58957e-05 | 0.00573964 | missense | ERCC6 | GRCh38.p7 | 10:49470298 | ACCAGGTGTGGAATT[C/T]GAGTTCCTTCAAACT | 2074 |
rs200500364 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537502 | CTATATATATATATA[C/T]ACACATACACACACA | 2074 |
rs200516416 | snp | A/G | 9.91801e-05 | 0.00704132 | missense | ERCC6 | GRCh38.p7 | 10:49461440 | ACCGCTGACGAGAGA[A/G]CCTCAGTGCTTTCAG | 2074 |
rs200517639 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460897 | CCATCTCTAAAAAAA[A/G]AAAAAAAAAAAGGAA | 2074 |
rs200542608 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507959 | CACATATCTGAATTC[C/T]TGATATATATACACT | 2074 |
rs200563217 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526143 | TATATATATATATAT[A/T]TATATATATATATAT | 2074 |
rs200572441 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537508 | ATATATATATACACA[C/T]ACACACACACACACA | 2074 |
rs200574805 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507965 | TCTGAATTCTTGATA[C/T]ATATACACTTTCCTG | 2074 |
rs200579505 | snp | C/T | 3.29489e-05 | 0.00405874 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473465 | AACTTCCCTGTTACA[C/T]TCACATGTTACCTCA | 2074 |
rs200634232 | snp | A/G | 0.00104169 | 0.0227983 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493093 | ATTAAAACAAAACAA[A/G]AAGGTACTGAAATAT | 2074 |
rs200638550 | snp | C/T | 0.00199808 | 0.0315444 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516267 | CCCCGAATAAATTGT[C/T]TGCACCCGTGACGAC | 2074 |
rs200697187 | snp | C/T | 0.000560252 | 0.0167276 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515910 | CCTTTGCCATCAATT[C/T]GATAATCAAATGTGC | 2074 |
rs200700501 | snp | C/T | 6.64077e-05 | 0.00576189 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516390 | CGCAATTTGGAAAAT[C/T]TGTCCACTGGATCCA | 2074 |
rs200769093 | snp | A/G | 0.00199792 | 0.0315431 | missense | ERCC6 | GRCh38.p7 | 10:49532820 | GCCCGTCACCCACAG[A/G]ACGAAAGGAGAGGTA | 2074 |
rs200770507 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484291 | CTCAAAAAAAAAAAA[A/G]GAAAAAAAAAAAAAG | 2074 |
rs200818896 | snp | A/G | 0.00016478 | 0.0090754 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524091 | ATCTTCCCACTTTCC[A/G]ACCTCCTCCTCCTCC | 2074 |
rs200832611 | snp | A/C/T | 0.000214638 | 0.0103574 | missense | ERCC6 | GRCh38.p7 | 10:49493118 | AAATATTGTGTTACC[A/C/T]TTTTGTGGGTATAGG | 2074 |
rs200850660 | snp | C/T | 6.58989e-05 | 0.00573978 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516951 | GTGTGCAACAAAGAA[C/T]CTGGCAGATTATTTA | 2074 |
rs200862492 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493005 | AACTTTAAATGCAGG[-/A]AAAAAAAACACAGGA | 2074 |
rs200876040 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490118 | CAGAAGCCTAAAAAT[G/T]TCTTTATCAGATTTC | 2074 |
rs200880466 | in-del | -/A | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455040 | ATAAACAAAAAAAAA[-/A]TGGAAAGACTGAATT | 2074 |
rs200885276 | snp | A/C/G | 1.64792e-05 | 0.00287042 | missense | ERCC6 | GRCh38.p7 | 10:49470791 | ATATGTTAGAAGCAG[A/C/G]GAACTTCTTGCGTTT | 2074 |
rs200893601 | snp | A/G | 0.000399281 | 0.0141238 | missense | ERCC6 | GRCh38.p7 | 10:49532699 | CCCTGCAGCTCAAGG[A/G]CCTGGGCGCTAGGCT | 2074 |
rs200906205 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506409 | ACTATGTAACAAAAA[A/T]TAGATTTATAATTAC | 2074 |
rs200914470 | snp | A/G | 6.59087e-05 | 0.00574021 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516677 | ATCAAGAAAAAGTTC[A/G]AGAATTTCTGTGGGA | 2074 |
rs200925890 | snp | C/T | 0.000166495 | 0.00912248 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516141 | GACGCACCGACACCA[C/T]ATTCCTCATGTTTAG | 2074 |
rs200950339 | snp | A/G | 0.000538766 | 0.016404 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482910 | AATTTACCTTTTAGC[A/G]ATCGCCATTCCTACC | 2074 |
rs201062280 | snp | C/G | 4.94238e-05 | 0.00497086 | missense | ERCC6 | GRCh38.p7 | 10:49532872 | ACCACTTTCTTGCTT[C/G]ATTGCCATTTCTTCA | 2074 |
rs201067325 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469488 | TATTATTCCAACTGA[-/T]TTTTTTTTTGAGACC | 2074 |
rs201098951 | snp | A/G | 1.65031e-05 | 0.00287251 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472370 | GTGGCCACTGTGTGC[A/G]CTGACCGGTGGTAGA | 2074 |
rs201099950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515285 | CACTGCTACACTGTA[C/T]ATAATGTATAAAACT | 2074 |
rs201116894 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460570 | TGCATGCTTATTCTT[C/T]CACAGCCATGCCATT | 2074 |
rs201246957 | snp | C/G | 0.00199792 | 0.0315431 | missense | ERCC6 | GRCh38.p7 | 10:49532715 | CCTGGGCGCTAGGCT[C/G]TACTGCCTGGATCTG | 2074 |
rs201267890 | in-del | -/CTC | 0.0387552 | 0.1337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513854 | TTATTCTCTCTCTCT[-/CTC]TTTTTTTTTTAACAA | 2074 |
rs201281422 | snp | C/G | 0.000181241 | 0.00951777 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473442 | CTCCACGTACAGCAG[C/G]ACCACTCAACTTCCC | 2074 |
rs201323217 | snp | C/T | 3.29484e-05 | 0.00405871 | missense | ERCC6 | GRCh38.p7 | 10:49532628 | GGATGGCATTGTCCA[C/T]CTGCTGAAGCACTCC | 2074 |
rs201346089 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537510 | ATATATATACACATA[C/T]ACACACACACACACA | 2074 |
rs201375732 | snp | C/T | | | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470486 | AGCCTGGCTGGGTCT[C/T]TCTCTTTTGTAAGAA | 2074 |
rs201383229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530876 | TCTATTTTGCACTCT[A/G]ATAACATTTTTATAG | 2074 |
rs201406273 | snp | G/T | 0.000380773 | 0.0137928 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516266 | TCCCCGAATAAATTG[G/T]TTGCACCCGTGACGA | 2074 |
rs201468099 | snp | C/T | 0.0002636 | 0.0114774 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516929 | ATCTTGAATAAGATA[C/T]GCAGCTGTGTGCAAC | 2074 |
rs201486862 | snp | C/T | 8.2464e-05 | 0.00642069 | missense | ERCC6 | GRCh38.p7 | 10:49482719 | TTGAATATCCCCCCA[C/T]GGTGATGGGGACGGA | 2074 |
rs201487601 | snp | A/C | 0.000497413 | 0.0157626 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482884 | TGAGGAAAGGAAGCA[A/C]CTTTTTATTAAATTT | 2074 |
rs201495726 | snp | C/T | 0.00199795 | 0.0315433 | missense | ERCC6 | GRCh38.p7 | 10:49461353 | CAGCAATCTCTTACT[C/T]TTTTCCTGCTGGTGC | 2074 |
rs201496784 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495569 | TCCAAACCACCACAC[A/G]CTAGAAATCTCACTG | 2074 |
rs201617781 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507960 | ACATATCTGAATTCT[A/T]GATATATATACACTT | 2074 |
rs201740839 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516871 | GAGAGTCATCTTTAG[A/G]TGCGTATGAGGGATC | 2074 |
rs201744511 | in-del | -/AAAG | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504192 | TAAAACGCAATCATA[-/AAAG]AAAAATGGAGACTCT | 2074 |
rs201778608 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537504 | ATATATATATATATA[C/T]ACATACACACACACA | 2074 |
rs201813523 | snp | C/T | 0.000345881 | 0.0131461 | missense | ERCC6 | GRCh38.p7 | 10:49458904 | ATAGTTCTCGGAAGA[C/T]ACAAGACTGTGATGC | 2074 |
rs201814055 | snp | G/T | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516630 | CAAGCATATAAGTTG[G/T]AGTACTTGACAATGA | 2074 |
rs201815633 | in-del | -/TATATATATATATATATATATATATATA | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526118 | ATATTTATATATTTT[-/TATATATATATATATATATATATATATA]TATATATATATATAT | 2074 |
rs201871784 | snp | C/T | 0.00036245 | 0.0134571 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470771 | TGATGTGGCATCATT[C/T]ACAGATATGTTAGAA | 2074 |
rs201894064 | snp | C/T | 0.000148335 | 0.00861078 | missense | ERCC6 | GRCh38.p7 | 10:49483503 | CAATGAGCAACATCT[C/T]GAATTAGTTTCTCCT | 2074 |
rs201924626 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526145 | TATATATATATATAT[A/T]TATATATATATATAT | 2074 |
rs201930958 | snp | A/C/T | 0.000263559 | 0.0114769 | missense | ERCC6 | GRCh38.p7 | 10:49478436 | GGATTTATGGTATCT[A/C/T]GTAAGACACATGCAC | 2074 |
rs201934795 | snp | A/G | 0.000991457 | 0.0222429 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470924 | CACTAATACTATATT[A/G]TATCATCTTGTGCAA | 2074 |
rs201935629 | snp | C/T | 1.6522e-05 | 0.00287414 | missense | ERCC6 | GRCh38.p7 | 10:49506005 | GCAGTCTCAGTTTAT[C/T]CCATCTCCTACCATG | 2074 |
rs201939424 | snp | C/G | 3.29734e-05 | 0.00406025 | missense | ERCC6 | GRCh38.p7 | 10:49474149 | GATCTTCTTCTAGTT[C/G]ATCATCAGGAAGACC | 2074 |
rs202001914 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534149 | AAAAAAAAAAAAAAA[-/C]AAAAACAAAAAAAAA | 2074 |
rs202046174 | snp | A/T | 0.00199802 | 0.0315439 | missense | ERCC6 | GRCh38.p7 | 10:49476287 | GACTTTATGCTGCTC[A/T]TCTGTAAGACGGCAA | 2074 |
rs202080674 | snp | A/G | 0.00199803 | 0.031544 | missense | ERCC6 | GRCh38.p7 | 10:49482848 | CAGACAGAATGATCC[A/G]ATGAGGGGTGCGAAA | 2074 |
rs202089085 | in-del | -/AAG | 0.0383715 | 0.133092 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478566 | CCTTAAAAAAAAAAA[-/AAG]AATAACCAACAGCTG | 2074 |
rs202116235 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511011 | TTTAGAATCTTATAA[A/C]AAAAAAAAAAAAAGA | 2074 |
rs202126438 | snp | C/T | 6.59304e-05 | 0.00574116 | missense | ERCC6 | GRCh38.p7 | 10:49528422 | GCATCCTCACCTGCA[C/T]CCTCCTCCAGACTGG | 2074 |
rs202160105 | snp | A/T | 0.000185496 | 0.00962879 | missense | ERCC6 | GRCh38.p7 | 10:49461499 | GCCTCCACCAGTACA[A/T]AATCTGGGCTGGCTC | 2074 |
rs202166883 | in-del | -/AACAAACA | 0.0391387 | 0.134304 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496811 | GAGACTCTGTCTCAG[-/AACAAACA]AACAAACAAACAAAA | 2074 |
rs202175975 | snp | C/T | 3.30442e-05 | 0.0040646 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524678 | TGTTTCTGAGGGATC[C/T]GGGTACCAAAAGGTG | 2074 |
rs202245893 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49458911 | TCGGAAGACACAAGA[C/T]TGTGATGCAGATAAC | 2074 |
rs202246230 | snp | C/T | 0.000215173 | 0.0103702 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516231 | CCACACCAAAACTTA[C/T]AGCCAAACCGAATGG | 2074 |
rs267602507 | snp | A/G | | | missense | ERCC6 | GRCh38.p7 | 10:49470355 | TTAGGCTTTTGCTTT[A/G]GTCTCAGATGTTTCT | 2074 |
rs267602508 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524149 | TTCCCCAGAACTTGG[A/G]AAAAAGTCATCATCA | 2074 |
rs267602509 | snp | A/G | | | stop-gained | ERCC6 | GRCh38.p7 | 10:49532724 | TAGGCTCTACTGCCT[A/G]GATCTGATGTCGGTC | 2074 |
rs367546930 | snp | C/T | 3.29484e-05 | 0.00405871 | missense | ERCC6 | GRCh38.p7 | 10:49483422 | ATCACATAGTGCCAG[C/T]CATACCTGCTAATGT | 2074 |
rs367552064 | snp | A/G | 1.65203e-05 | 0.002874 | missense | ERCC6 | GRCh38.p7 | 10:49461434 | CCAGACACCGCTGAC[A/G]AGAGAGCCTCAGTGC | 2074 |
rs367552949 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540290 | GTGATCCACCCGCCT[C/T]GGCCTCCTAGAGTTC | 2074 |
rs367598256 | in-del | -/GAA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504195 | AACGCAATCATAAAA[-/GAA]AAATGGAGACTCTAT | 2074 |
rs367673985 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532995 | TAAAAGGAAAAAAAT[G/T]TATAAGCCTTTTCGT | 2074 |
rs367763158 | snp | C/T | 1.6643e-05 | 0.00288465 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505870 | ATAGAAAGGAAAGAA[C/T]ATATGGTACATACTT | 2074 |
rs367812837 | snp | A/G | 1.7291e-05 | 0.00294027 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524774 | AGACTGGATGGCCCC[A/G]GCTCTGAAAGAACAA | 2074 |
rs367864930 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511087 | AAATAAAAATTGTGT[A/G]AGTGATTTAAGTCTG | 2074 |
rs367884208 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533788 | AGCCTGGGCAAAAGA[A/G]CAAGACCTTGTAAAA | 2074 |
rs367896949 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457343 | TAAAAACAAAAGAAA[C/T]GAACAAGCTATAATC | 2074 |
rs367963492 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481598 | GGGATGCACAGAAAC[C/T]GTGCCTCCCACCCAG | 2074 |
rs367965088 | snp | C/T | 6.59152e-05 | 0.00574049 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524408 | ACTTTCCCCTGGAAC[C/T]GCAAAGCCCTCTTCT | 2074 |
rs367973449 | snp | A/C | 1.66067e-05 | 0.00288151 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516346 | GAACAAATTTCATGC[A/C]TCTCTCATTAAGTTT | 2074 |
rs367984534 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461384 | ACCAGAAATCCCCCT[A/G]TGGCCAGTCCAGGTG | 2074 |
rs367986704 | in-del | -/CAAACAAA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496825 | GAACAAACAAACAAA[-/CAAACAAA]ATACAATTTTTACAA | 2074 |
rs368037080 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473627 | TTTGCAAAGCAAATA[C/T]ACATTCCCAGTGAGT | 2074 |
rs368064456 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498450 | GAGGAGGATGTGTTA[C/T]AAAGTTGTTAGGAAG | 2074 |
rs368100922 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519570 | TGCACCAGGTCATCT[A/G]AGGAGACTCAGGCAC | 2074 |
rs368118007 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463241 | AATTTTAATATAATA[C/T]GTTTATCAATTTTGT | 2074 |
rs368188837 | snp | A/G | 4.94205e-05 | 0.0049707 | missense | ERCC6 | GRCh38.p7 | 10:49478410 | CTGACTTCATTCTCC[A/G]CAGTAGGTATGGATT | 2074 |
rs368221420 | snp | A/T | 8.23825e-05 | 0.00641751 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49517016 | AGAAACAGGTGCTGT[A/T]GCATTTTCAGGTGGT | 2074 |
rs368235215 | in-del | -/A/AA/AAA | 0.233593 | 0.256414 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537342 | GCAAGACTCCGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 2074 |
rs368315377 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49483140 | CCCCTACAAGAGACA[C/T]TAAATAACATGAACA | 2074 |
rs368328801 | snp | C/T | 1.66418e-05 | 0.00288455 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516105 | GCCTCTGTAAGTGCC[C/T]CACTAAACTGAAGGA | 2074 |
rs368414783 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497170 | GGCAGGGCCTGTCCA[C/G]GTGCCCCTTGAGCTC | 2074 |
rs368470553 | snp | A/G | 3.31411e-05 | 0.00407056 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516280 | GTTTGCACCCGTGAC[A/G]ACCAAAATAAGGAAC | 2074 |
rs368474968 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492535 | AATACAACGTATCTA[C/T]GCTACCCACAGGAGC | 2074 |
rs368483062 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490426 | GTGGCACAGTCCAGG[C/T]TCACTGCAACCTCCG | 2074 |
rs368503359 | snp | A/G | | | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515242 | CCATTGTTATGTGAC[A/G]TTCCAAAATTGGAAC | 2074 |
rs368563985 | snp | A/C/G | 3.29833e-05 | 0.00406088 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515820 | TAACGACTGACAAGA[A/C/G]ACAGGGGATGGATAC | 2074 |
rs368615079 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515315 | TATGTTTCTTATCTC[A/T]GGAGGTGGTGACACC | 2074 |
rs368619474 | snp | A/T | 1.65214e-05 | 0.0028741 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470950 | TGCAATTGATTACTT[A/T]AAATTAAATGATTTT | 2074 |
rs368646756 | snp | C/T | 3.29473e-05 | 0.00405864 | missense | ERCC6 | GRCh38.p7 | 10:49473547 | ATCTTGAGATAGGTA[C/T]ACTTTTGGGCTCTAA | 2074 |
rs368684611 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507735 | ACTGTGGAAGGAGTC[A/G]GGAGGATATACTACT | 2074 |
rs368685485 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535473 | TGGGGCCTGCTGATT[-/A]TTTTCAAGAGGAAGG | 2074 |
rs368720674 | snp | C/T | 6.61474e-05 | 0.00575059 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516519 | TGTTCCCAAAACATA[C/T]GCCTTCTAGGAACTG | 2074 |
rs368728467 | snp | A/G | 0.000153988 | 0.00877328 | missense | ERCC6 | GRCh38.p7 | 10:49474074 | GACCCTGCTTGTGCC[A/G]TATTTTCAACAAAGA | 2074 |
rs368738108 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458624 | TTTCTCCTTTAGCTA[A/G]CATTATTAAAACTTT | 2074 |
rs368813647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510238 | CATCAATGGAACCCT[C/G]AAAGCTAGTTGCTGC | 2074 |
rs368828623 | snp | A/C/T | 9.88593e-05 | 0.00703004 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516874 | AGTCATCTTTAGGTG[A/C/T]GTATGAGGGATCATC | 2074 |
rs368880078 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538923 | GCTGGGCCCCGACAC[C/T]CCCTGCCCGACATTC | 2074 |
rs368887569 | snp | C/T | 0.000347939 | 0.0131852 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488209 | AAAGGGCTGCTGTTA[C/T]TATGGAGGCTCAAGA | 2074 |
rs368892598 | snp | C/T | 0.000215155 | 0.0103697 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532504 | ATCCCTGTCATGTTT[C/T]ACCACCACTTTGAAA | 2074 |
rs368907663 | snp | G/T | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49470364 | TGCTTTGGTCTCAGA[G/T]GTTTCTCCAGGGTCT | 2074 |
rs369030008 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530515 | GTGTGTCTATGTATG[C/T]GTGTTTTTTTAAATG | 2074 |
rs369030114 | snp | C/T | 0.000148467 | 0.00861461 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49493165 | AATTGCCACTCTGAA[C/T]GGAGGCCACCACGTG | 2074 |
rs369073783 | in-del | -/TGCTGCTTTGGTGGGTAAGGGTGTGGATACGCTTA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473383 | AAGCCCAGATGTCAA[lengthTooLong]GTCCTTTCCCTCCAC | 2074 |
rs369182625 | in-del | -/AAT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533620 | CAGCCTGGGAAAGAT[-/AAT]GAGACCTTGTCTCTA | 2074 |
rs369196480 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533180 | AATAAGAAAAATTAA[A/C]CAGAAAAAGAAATGC | 2074 |
rs369223136 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480714 | AGTTAACATCACCCA[C/T]AGTGGAACAAACAGA | 2074 |
rs369244603 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456148 | ACTTCAAAAGACAGT[A/G]GCTTAAGCAAGTCAG | 2074 |
rs369246361 | snp | C/T | 4.95847e-05 | 0.00497895 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472342 | TCAAGACTCTGGGAA[C/T]GCACAGCCAAGAGTG | 2074 |
rs369256002 | snp | C/T | 3.29592e-05 | 0.00405938 | missense | ERCC6 | GRCh38.p7 | 10:49528438 | CCTCCTCCAGACTGG[C/T]GTGATCTAGTTCAAT | 2074 |
rs369274690 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506703 | TATTTCATCTAAATA[C/T]CTGAAAGTCTTAGCA | 2074 |
rs369276778 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49493973 | CAGCAAAATCAAGAG[C/T]CTCAACAGCACCCAT | 2074 |
rs369295816 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523726 | AGGGTGACTGTCGGT[A/G]TAAAGGCGACACAGC | 2074 |
rs369352007 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513455 | TTTAATCTTTACAAC[A/C]TAATAAGGGAGATAC | 2074 |
rs369357016 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465566 | ATGTCCCAGCCAAAT[C/T]TCATCTTGAATTGTA | 2074 |
rs369384047 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490880 | GCACAGAAAGCTCAT[C/G]CACTGTAAAAAGAAA | 2074 |
rs369437807 | snp | C/T | 0.000428562 | 0.0146321 | missense | ERCC6 | GRCh38.p7 | 10:49482731 | CCATGGTGATGGGGA[C/T]GGAGAACTGCTCCAT | 2074 |
rs369441175 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49471087 | TTTTGGGTCTTTTAG[C/T]ACTCTATTTGTCAAA | 2074 |
rs369444705 | snp | A/G/T | 3.2954e-05 | 0.00405908 | missense | ERCC6 | GRCh38.p7 | 10:49459137 | TTAGCCAAGAGTGAG[A/G/T]AGGAAGCGAGGGGCC | 2074 |
rs369488242 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482682 | TTATCATCCTAATAT[G/T]TTACCTGTACTGGGG | 2074 |
rs369489725 | snp | C/G | | | missense | ERCC6 | GRCh38.p7 | 10:49470374 | TCAGATGTTTCTCCA[C/G]GGTCTCTTCTTCTGC | 2074 |
rs369522698 | snp | A/G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518747 | CCCAAGCCAGGGTTC[A/G/T]ATGGGGCCCTGGCCA | 2074 |
rs369622311 | snp | A/C/G | 0.000149376 | 0.00864109 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528375 | CTACAGGCATCAGGC[A/C/G]TCAATTCAAGAACAC | 2074 |
rs369626385 | snp | C/T | 0.000240121 | 0.0109546 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493090 | GGCATTAAAACAAAA[C/T]AAAAAGGTACTGAAA | 2074 |
rs369634749 | snp | C/T | 1.73924e-05 | 0.00294888 | missense | ERCC6 | GRCh38.p7 | 10:49461524 | TGGCTCCATCCATGA[C/T]GGCATCGTGCTTCAT | 2074 |
rs369647659 | in-del | -/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521814 | AGCAGGATCCAAAGG[-/G]CGACTGCCCAGTTCC | 2074 |
rs369683176 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492117 | GCAAAATTCCATCTC[A/G]CCTTATTTGTGCTAC | 2074 |
rs369686359 | snp | A/G | 6.69916e-05 | 0.00578717 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515372 | ACACTTCACATGTAA[A/G]GCAACATCACATTTT | 2074 |
rs369745517 | snp | A/T | | | missense | ERCC6 | GRCh38.p7 | 10:49470434 | GCTTATAAAAATTAT[A/T]TTCCATTTGTTTATT | 2074 |
rs369811624 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530199 | AAAACTAAGGAAGTG[C/T]GCCCAAGTGAGGCAA | 2074 |
rs369822441 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506971 | TAAAAAAAAAACTCA[C/T]AGGAAGCGAGTAAGA | 2074 |
rs369833110 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538731 | AGCTGGGTCGCTGGC[C/G]GGCCAGGGACTCAAG | 2074 |
rs369864700 | snp | A/G | 6.63768e-05 | 0.00576056 | missense | ERCC6 | GRCh38.p7 | 10:49474226 | ATTTTTCTTAGGGCT[A/G]TAAGTCCGGAGAAAA | 2074 |
rs369887881 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49532135 | CCAAGGACTGAACAC[C/T]AAGTTTGGGGACAGT | 2074 |
rs369906037 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478555 | TTGCTTCCATTCCTT[-/A]AAAAAAAAAAAAGAA | 2074 |
rs369915877 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471372 | CTTTTTCAACCTCCA[A/T]GATCTAACACATTTC | 2074 |
rs369937757 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510170 | ACCCAGCACAACCAG[C/T]TGAACGACACCAGGA | 2074 |
rs369987164 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490638 | GATTACAGGCATGAG[A/C]CACCACGCCCGGACA | 2074 |
rs370067221 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458775 | TAATCAGAAATGCCC[A/G]TTAGAAAAAGGGACT | 2074 |
rs370092075 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455897 | CTTACTGTTGGCAAG[A/G]GTTTGGAGAAATGGG | 2074 |
rs370101518 | snp | A/G | 6.59044e-05 | 0.00574002 | intron-variant, stop-gained | ERCC6, PGBD3 | GRCh38.p7 | 10:49516823 | TTGATGGTGGAGGTT[A/G]CTGCACAGTAAACGT | 2074 |
rs370105701 | snp | A/G | 8.2752e-05 | 0.00643189 | missense | ERCC6 | GRCh38.p7 | 10:49476298 | GCTCATCTGTAAGAC[A/G]GCAAAATAAGACCTA | 2074 |
rs370123825 | snp | C/T | 3.32668e-05 | 0.00407827 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459252 | ATAAAAAGAAGACCA[C/T]TATACTGATATATTT | 2074 |
rs370145967 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519205 | GTCATACCTAAATAT[C/T]GCACCTTCTACTCAA | 2074 |
rs370183296 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539655 | GGCAGGCGAGAATTT[C/T]ACCGTGGTGCGTTTG | 2074 |
rs370236505 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499988 | CTTCATTCAAAAACA[A/C]GAGAGAGAGCAAGCT | 2074 |
rs370242712 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477667 | CCAGCTAGCTCCTCC[A/T]CTTCTACCCTCCTCC | 2074 |
rs370285377 | snp | A/C/T | 8.27882e-05 | 0.00643335 | missense | ERCC6 | GRCh38.p7 | 10:49459230 | TCCTTTTTCATGATG[A/C/T]CATCCTATAAAAAGA | 2074 |
rs370292341 | snp | A/C | 1.6476e-05 | 0.00287014 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524138 | GCTTCAGCTTCTTCC[A/C]CAGAACTTGGGAAAA | 2074 |
rs370332660 | snp | A/G | 1.65091e-05 | 0.00287303 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515994 | TGATCCTTTCTCACT[A/G]TACCTGTTGCCTGAT | 2074 |
rs370357065 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503121 | AAGAGTTGTTGGACC[C/T]ATGTAGGATGGAGGC | 2074 |
rs370703900 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492195 | CATGAACACAAACAC[A/C]ACAGGAATCCTGGAG | 2074 |
rs370718332 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478865 | AATCTCTGTTTATGA[C/T]CTTGTATTCTCCAAA | 2074 |
rs370757757 | snp | A/T | 1.64768e-05 | 0.00287021 | missense | ERCC6 | GRCh38.p7 | 10:49470681 | ACTCATGTGAGGGTC[A/T]TCTTTCAAAGGATCA | 2074 |
rs370851590 | in-del | -/TCCA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487566 | CCCAGAGAAAAACCA[-/TCCA]CCTTTAGCACCTCAC | 2074 |
rs370872469 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525823 | CCTCCCAGCCTCTAC[A/G]CCCCCCAAGATAATG | 2074 |
rs370878573 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520227 | TTTAAAAGTCCTGCC[C/T]GGTGACCCCACGCTA | 2074 |
rs370880233 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492295 | CCTGGGCCCCGAGAA[C/T]GAACTCAAGAGCTCA | 2074 |
rs370920613 | snp | A/T | 1.64743e-05 | 0.00287 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516970 | GCAGATTATTTATTG[A/T]TCCACCTTCTTCATC | 2074 |
rs370923028 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483322 | TCTCCACTTGGAAAT[C/T]TCCCTTGTTAAAAGA | 2074 |
rs370925858 | snp | A/G | 9.9185e-05 | 0.0070415 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524252 | TCTCCAGACAGGTCC[A/G]CCTCTGCCCCCTCCA | 2074 |
rs370938370 | snp | C/T | 4.98832e-05 | 0.00499391 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461348 | GCATGCAGCAATCTC[C/T]TACTTTTTTCCTGCT | 2074 |
rs370993141 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463682 | GAACCCAGTGGGAGG[A/T]GATTAATTATGAAGA | 2074 |
rs371055602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505783 | CAAATTGCTGCAAGT[A/G]CCTTCAGGGCCCACA | 2074 |
rs371059775 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501663 | AAACCACTTGAATTA[A/C]AAGATGATAGGTTAG | 2074 |
rs371061152 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468518 | CATTGTTTCACATGG[A/G]AGGGTAAATGTTAAT | 2074 |
rs371079288 | snp | C/T | 0.000118304 | 0.00769013 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476318 | AATAAGACCTACGGA[C/T]GGGAAAAACAAGGAA | 2074 |
rs371085930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535895 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCTGAG | 2074 |
rs371095448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479801 | CTGCTCTCTCCTGCA[C/T]GCCACCCCATGGAGA | 2074 |
rs371100244 | snp | A/C/G/T | 0.0003459 | 0.0131469 | missense | ERCC6 | GRCh38.p7 | 10:49532655 | CTCCCTGTTCCAGCA[A/C/G/T]GTCCTGGTCATAGAC | 2074 |
rs371101734 | snp | A/G | 0.00165104 | 0.0286843 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500488 | AGCAATACATCTGAT[A/G]AAATATTAATTGAGC | 2074 |
rs371106084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484701 | GCTATAATCTCACCA[C/T]TGCATTCCAGGCTAG | 2074 |
rs371109408 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | ERCC6 | GRCh38.p7 | 10:49470529 | TCATCAATGCTTTCA[C/T]CACCAGATGGCATAG | 2074 |
rs371122072 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537214 | CTGGGCATGGAGGCG[C/T]GCGCCTGTAATCCCA | 2074 |
rs371140923 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475057 | AAGTCAGGAACATTG[-/G]TAAACCTCCCCAGAG | 2074 |
rs371202047 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518812 | AGTATTATCTTCGCA[A/G]GAGATTATGTCTCAC | 2074 |
rs371329841 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520927 | GGCAAATGCGTAACA[C/T]TGTTAATTTGGATAA | 2074 |
rs371401802 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506550 | TAACTGGGGGAAGAG[A/G]CATCAGCAATATACA | 2074 |
rs371426218 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528117 | TTAATCATGATGCTA[C/G]TTGTCTTTATCAAAT | 2074 |
rs371499959 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513989 | ATCTGTTACATAATA[C/T]TGTCTTCAAAAAAGT | 2074 |
rs371521642 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502787 | CAGAGAAGCTGTTCA[A/G]TATCTGATACTGCAC | 2074 |
rs371522486 | snp | A/G | 1.65438e-05 | 0.00287605 | missense | ERCC6 | GRCh38.p7 | 10:49460389 | TGGCACTTCTCTGTT[A/G]GAGATGTTGATGAAG | 2074 |
rs371533699 | snp | A/C/G | 6.60375e-05 | 0.00574587 | missense, synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461422 | CAGACACTGCTCCCA[A/C/G]ACACCGCTGACGAGA | 2074 |
rs371544606 | snp | A/C/T | 4.94265e-05 | 0.00497104 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524039 | CAGACCGACCTTAAC[A/C/T]GCTGCTTATAATAAT | 2074 |
rs371570769 | snp | C/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457528 | TCACATGGATGAGCA[C/G]ACAGAAGATCTGGAC | 2074 |
rs371669686 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508433 | TACAGGCATCTTGTC[A/G]CCACAGAACTCAGCA | 2074 |
rs371718837 | snp | A/G | 0.000625184 | 0.0176692 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524804 | ATAGCAATGCGTTTC[A/G]CACTAGCATGAAACT | 2074 |
rs371739894 | snp | A/C | 4.98095e-05 | 0.00499022 | splice-donor-variant | ERCC6 | GRCh38.p7 | 10:49505883 | AACATATGGTACATA[A/C]TTAAAAAGCTTTTTG | 2074 |
rs371753975 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515403 | TCACATCGAAAAGTT[G/T]TGTTCTTATGACATT | 2074 |
rs371790548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477062 | GTCCTGCTCCAGGGG[A/G]TCCTCTACGCATGCC | 2074 |
rs371807807 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529432 | GTCTCAAGTTTGATG[C/T]TCTACACCCTTGAAA | 2074 |
rs371856179 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470141 | AGCCTACTCATTTTC[C/T]AATCCTAGCATCCCT | 2074 |
rs371856191 | in-del | -/ACAA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537534 | CACACACACACACAC[-/ACAA]AAATATAATTGTGGT | 2074 |
rs371898033 | snp | C/T | 3.30682e-05 | 0.00406608 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516504 | TGCACATCTGTTCTT[C/T]GTTCCCAAAACATAC | 2074 |
rs371906100 | snp | C/G | 0.000115857 | 0.00761018 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473993 | GCTGTCATAAAGAAC[C/G]AGCCTGTTTCCCGTC | 2074 |
rs371906160 | snp | A/C | 0.000164728 | 0.00907398 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524521 | CACTGGGGCTGGAGG[A/C]GTGACTGGGGCTGGA | 2074 |
rs371911893 | snp | C/T | 1.64754e-05 | 0.00287009 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483330 | TGGAAATCTCCCTTG[C/T]TAAAAGAGGTCATAC | 2074 |
rs371917303 | snp | C/T | 4.97409e-05 | 0.00498678 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528381 | GCATCAGGCATCAAT[C/T]CAAGAACACAGAGAA | 2074 |
rs371934189 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473605 | GTTTGGAGGTGGGGG[A/G]TAGGAGTTTGCAAAG | 2074 |
rs371978640 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494993 | CCAGGTTTCACTTAG[A/G]TGCAGTCAAATATCC | 2074 |
rs371982149 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515316 | ATGTTTCTTATCTCA[A/G]GAGGTGGTGACACCT | 2074 |
rs372041999 | snp | G/T | 4.95299e-05 | 0.00497619 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470962 | CTTTAAATTAAATGA[G/T]TTTATGTAATACCTG | 2074 |
rs372092048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531910 | AGCTCAACCCCTCCC[A/G]CTTCCCCTCTCCTGT | 2074 |
rs372100122 | snp | A/C | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458068 | GTTTTTATGTACCTA[A/C]TTTTGGCTTTAATTT | 2074 |
rs372100845 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494223 | TTAACCTCTGGGAAC[A/G]TCAGTTTTTCATTTT | 2074 |
rs372113037 | snp | G/T | 1.79075e-05 | 0.00299223 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515320 | TTCTTATCTCAGGAG[G/T]TGGTGACACCTGCTA | 2074 |
rs372120121 | snp | C/T | 3.29658e-05 | 0.00405978 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517032 | GCATTTTCAGGTGGT[C/T]GTATCACTATAGCAC | 2074 |
rs372128351 | snp | C/T | 3.29473e-05 | 0.00405864 | missense | ERCC6 | GRCh38.p7 | 10:49478431 | GGTATGGATTTATGG[C/T]ATCTCGTAAGACACA | 2074 |
rs372159714 | in-del | -/AAAT | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537385 | AATCATACATTTAAC[-/AAAT]AGTTACTGAGAGTTA | 2074 |
rs372186831 | snp | C/T | 2.58408e-05 | 0.0035944 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488218 | CTGTTATTATGGAGG[C/T]TCAAGAGACCAATCC | 2074 |
rs372229103 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469676 | GAACACAGTGACTGC[C/T]AAGGGATCACTAAGC | 2074 |
rs372229369 | snp | C/T | 3.29478e-05 | 0.00405867 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473474 | GTTACATTCACATGT[C/T]ACCTCATTGTATCTC | 2074 |
rs372233524 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484278 | GTCAGACTCTGCCTC[-/A]AAAAAAAAAAAAAGA | 2074 |
rs372285026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520104 | AACTGATATACAAAC[C/T]GCATCAGCCAAAAGC | 2074 |
rs372298339 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479624 | TTTCAGAATTTAAAA[A/G]CATAGTCCCACTGAG | 2074 |
rs372302252 | in-del | -/ACTTTT | | | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514873 | GATACTTGGTGTTTT[-/ACTTTT]CTTATCTTCCTTTTT | 2074 |
rs372372920 | snp | G/T | 1.6582e-05 | 0.00287936 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516299 | AAAATAAGGAACCAT[G/T]AATTCATCAAAGCTG | 2074 |
rs372404036 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502469 | AGGAACCAACTGCTG[A/T]GGAGGCACCAGGCCA | 2074 |
rs372408108 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490502 | TAGGACTATAGGCGT[A/G]TGCCACCACAACCAG | 2074 |
rs372494513 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524140 | TTCAGCTTCTTCCCC[A/G]GAACTTGGGAAAAAG | 2074 |
rs372560390 | snp | A/T | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539267 | GGTGGCTTGCGAAGG[A/T]CGCTTCGCCCCTAGC | 2074 |
rs372584339 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510964 | AAAATGACCCATAAT[A/G]AGGGTGGCTGCAACA | 2074 |
rs372591901 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482868 | GGGGTGCGAAACTAT[G/T]TGAGGAAAGGAAGCA | 2074 |
rs372633807 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465515 | TGAAGATATGAGATA[C/T]GGGAGGGGCCAGAGG | 2074 |
rs372671521 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467047 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 2074 |
rs372671547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535000 | AGGTCACACGAGCAT[C/T]GAGCGAACTATATAT | 2074 |
rs372681812 | snp | A/G | 1.65102e-05 | 0.00287312 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49476239 | TCCATTGAGAATCCT[A/G]TAAACTTCTTTGGAA | 2074 |
rs372743065 | snp | A/T | 1.64749e-05 | 0.00287005 | missense | ERCC6 | GRCh38.p7 | 10:49470250 | GCCTCACTCTTGTTT[A/T]CACTGTCTTGCTTCT | 2074 |
rs372864293 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486224 | CAGCCTCTCTGAGAG[A/G]AAGTCAGATCAAAGA | 2074 |
rs372905926 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522580 | CATCAAATTAACTAA[A/C]CCCACATTTAAAATT | 2074 |
rs372926697 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499249 | ATCTCCAAGTGTTTT[A/C]TTCCCCTTCCTACAT | 2074 |
rs372945029 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | ERCC6 | GRCh38.p7 | 10:49482742 | GGGACGGAGAACTGC[C/T]CCATAAACACAGGCA | 2074 |
rs372990246 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526111 | TATTTATATATTTAT[A/T]TATTTTTATATATAT | 2074 |
rs373001458 | snp | A/G | 4.98269e-05 | 0.00499109 | intron-variant, stop-gained | ERCC6, PGBD3 | GRCh38.p7 | 10:49516376 | TGCTTATGAGAGGTC[A/G]CAATTTGGAAAATTT | 2074 |
rs373003422 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498689 | TTAATTGATTACAGC[G/T]GCTGTTCATTATTAG | 2074 |
rs373055738 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474444 | GATAGAACAAGTTCT[C/T]AGAAACAAAAAAATT | 2074 |
rs373071717 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506954 | ATGCTTTCAAACTAC[A/T]ATAAAAAAAAAACTC | 2074 |
rs373101592 | in-del | -/CT | 0.00914312 | 0.0669923 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504207 | AAAGAAAAATGGAGA[-/CT]CTATCAATCCTATTA | 2074 |
rs373146281 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49482123 | GGGTCTCTTCACTGC[A/G]CCCTGCCACATATGG | 2074 |
rs373161930 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457335 | AACCAAACTAAAAAC[A/G]AAAGAAATGAACAAG | 2074 |
rs373167596 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468739 | GAACACTCTGAGAAC[C/T]CGGATCCTAGTTCCT | 2074 |
rs373174504 | snp | A/G | | | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516659 | GAGTTCAATGACCTC[A/G]TCATCAAGAAAAAGT | 2074 |
rs373227647 | snp | C/T | 3.30213e-05 | 0.00406319 | splice-acceptor-variant | ERCC6 | GRCh38.p7 | 10:49472472 | GCTCGCTCCCGGGCC[C/T]GCAACAGAGAGAGAG | 2074 |
rs373277796 | snp | G/T | 9.88386e-05 | 0.00702919 | missense | ERCC6 | GRCh38.p7 | 10:49478428 | GTAGGTATGGATTTA[G/T]GGTATCTCGTAAGAC | 2074 |
rs373292756 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536008 | GTAATCCCAGCTACT[C/G]GGGAGGCTGAGGCAC | 2074 |
rs373471715 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475600 | CAATAGAGTCTTTTG[A/G]AGAAGACACTAGCTA | 2074 |
rs373471724 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524531 | GGAGGCGTGACTGGG[A/G]CTGGAGCTTTTCTAG | 2074 |
rs373513010 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464935 | GTGCAGAAGGAAAAT[A/G]TTGGGTTGGAGTCCC | 2074 |
rs373522295 | snp | A/C/G | 6.59711e-05 | 0.00574298 | missense | ERCC6 | GRCh38.p7 | 10:49493175 | CTGAACGGAGGCCAC[A/C/G]ACGTGTGAAATTCCT | 2074 |
rs373533137 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49532435 | GTCCTCCAAATAAAA[C/G]GTTCTACACATCTCC | 2074 |
rs373553169 | snp | C/T | 1.66866e-05 | 0.00288842 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459265 | CACTATACTGATATA[C/T]TTAATTTCTAGTTTA | 2074 |
rs373575223 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518808 | GAAGAGTATTATCTT[C/T]GCAGGAGATTATGTC | 2074 |
rs373618359 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485380 | TAAAATATAAAAGAA[A/G]AAGTTTAAAAAGAAG | 2074 |
rs373693554 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49472225 | AGCATATTTTAAAGG[A/G]AAAGAAAAAATACAA | 2074 |
rs373710355 | snp | A/G | 0.000378847 | 0.0137579 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483339 | CCCTTGTTAAAAGAG[A/G]TCATACCTGTTTGCA | 2074 |
rs373738673 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457024 | TCAATACAGTTTATG[C/T]TTCAGACACTATAAG | 2074 |
rs373742386 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467666 | AACCTCCCAGGCTCG[A/G]GCAATCCTCCCAGCT | 2074 |
rs373764035 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516066 | AAAAAGTTATTGAAT[A/G]CAAAATGGTATTGTC | 2074 |
rs373774673 | snp | A/C | | | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524639 | GATGCTTCATTAAGC[A/C]TGATTTTTCTGGGCT | 2074 |
rs373791746 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536009 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCACG | 2074 |
rs373863437 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537816 | CAACCTCCGCCTTCC[A/G]GGTTCAAGCGATTCT | 2074 |
rs373893264 | snp | C/T | 1.65282e-05 | 0.00287469 | missense | ERCC6 | GRCh38.p7 | 10:49470883 | GTCTGAACATCTGAT[C/T]CAGTTCCTGTAAAGA | 2074 |
rs373904287 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507130 | GTCCAGTATCCATTA[C/T]AAAACCACACAGAGC | 2074 |
rs373922933 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534121 | CATAGGCAACAGAGT[A/G]AGACTCAATCTCAAA | 2074 |
rs374014916 | snp | C/G/T | 0.000148303 | 0.00861007 | missense | ERCC6 | GRCh38.p7 | 10:49532601 | CGAGCTGGGAGGCAC[C/G/T]GCTGGCCTCATGGAT | 2074 |
rs374124590 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457928 | AGGCGCAAGACGAAG[A/G]CAACTGGAGAGAAGA | 2074 |
rs374284894 | snp | C/T | 4.94768e-05 | 0.00497352 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515822 | ACGACTGACAAGACA[C/T]AGGGGATGGATACCA | 2074 |
rs374295019 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516085 | AATGGTATTGTCCAG[C/G]GTGTGCCTCTGTAAG | 2074 |
rs374304221 | snp | A/G | 0.000345875 | 0.013146 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478332 | CTTTAGGAATGCTTC[A/G]TTAACTCCTGGATTT | 2074 |
rs374363185 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524585 | TTCTTCCTTTCAAAA[G/T]ACAGTTTTGCTTGAT | 2074 |
rs374408908 | in-del | -/AA | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525235 | ATGTACCTAAAAAGG[-/AA]AAAAACATAAATGTC | 2074 |
rs374470147 | snp | A/G | 9.88386e-05 | 0.00702919 | missense | ERCC6 | GRCh38.p7 | 10:49473490 | ACCTCATTGTATCTC[A/G]TAATCAGTGGCTGTC | 2074 |
rs374490261 | snp | A/G | 0.000197742 | 0.00994143 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524193 | GCACTTTCTTCTGCC[A/G]TTTCCCGCCCTTGGG | 2074 |
rs374519405 | snp | G/T | 1.65356e-05 | 0.00287533 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516573 | ATTCCCAGAAAACAT[G/T]TGAATTCAGAGCTAG | 2074 |
rs374523249 | snp | C/T | 3.29582e-05 | 0.00405931 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474084 | GTGCCATATTTTCAA[C/T]AAAGACTCAACAACA | 2074 |
rs374548607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504783 | ATTTCAACTTCTACA[C/T]GGCTGTTCCTCTGTC | 2074 |
rs374594438 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516847 | TAAACGTAGATGGAA[C/G]TTCATCAGGAGAGTC | 2074 |
rs374639643 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467376 | TCACATCTTTACCAA[C/T]ACTTAGTATGGTCAG | 2074 |
rs374747149 | snp | A/G | 1.66065e-05 | 0.00288149 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472521 | CCTTCCCAATGACAA[A/G]CACTGACTATAAGAA | 2074 |
rs374791168 | snp | C/T | 4.94205e-05 | 0.0049707 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470366 | CTTTGGTCTCAGATG[C/T]TTCTCCAGGGTCTCT | 2074 |
rs374796817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531721 | ATGGTTAGCAGAAAA[C/T]ATGTCTTTGAAGTAC | 2074 |
rs374868176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477507 | CAAGCCTCACGGGCA[C/T]CTCTGTTGATGCCAC | 2074 |
rs374869620 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469990 | AAAGTTTCAAATTAT[G/T]CTAGGTCTTCAGAAA | 2074 |
rs374876100 | in-del | -/CA | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478043 | TTCACTGCTGTATCT[-/CA]GAGCCTAGGATCACG | 2074 |
rs374902547 | snp | G/T | 4.97146e-05 | 0.00498546 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473068 | AGCACACACACTTAA[G/T]ACCAGTTACAGTTCT | 2074 |
rs374906942 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506512 | GTCAAAATCACTGAA[C/T]CAGGTTCACATTACT | 2074 |
rs374960223 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467281 | ATATCACAAGGAAAG[C/T]GCATGCAACTGCCAA | 2074 |
rs375008842 | in-del | -/GTC | 3.29484e-05 | 0.00405871 | cds-indel, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524155 | AGAACTTGGGAAAAA[-/GTC]ATCATCAATCTCCTG | 2074 |
rs375032247 | snp | A/C | 6.59979e-05 | 0.00574409 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528408 | AGAAACTGCTCCTAG[A/C]ATCCTCACCTGCATC | 2074 |
rs375044889 | snp | C/G | 1.64776e-05 | 0.00287028 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470154 | TCTAATCCTAGCATC[C/G]CTGTGGCAAACGTAT | 2074 |
rs375074878 | snp | C/G | 1.71261e-05 | 0.00292622 | intron-variant, missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49517120 | TTCGAGGCATCTTGG[C/G]ACTAAAACGGAAAAA | 2074 |
rs375136439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519659 | ATGGGTCGGGGATTT[A/C]TCCCAGAGGCAATTA | 2074 |
rs375171495 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536189 | GAAATGTAGTTGGTG[C/T]GTAAGGAGTGGATGA | 2074 |
rs375175948 | snp | C/T | 6.8867e-05 | 0.0058676 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515353 | CAGTGTGATATTCAA[C/T]GGAACACTTCACATG | 2074 |
rs375181157 | snp | C/T | 0.000197752 | 0.00994168 | missense | ERCC6 | GRCh38.p7 | 10:49471056 | AGAGATCATTGGATT[C/T]GAAAAACCGCCTTTG | 2074 |
rs375195488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490287 | TAAAGGGCAACTTGG[A/G]GAAGAAGAATGATAG | 2074 |
rs375200016 | snp | C/G | 9.88419e-05 | 0.00702931 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516982 | TTGTTCCACCTTCTT[C/G]ATCTCCTGATTCCTC | 2074 |
rs375218362 | snp | A/G | 1.66574e-05 | 0.0028859 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516156 | TATTCCTCATGTTTA[A/G]TATTTGGGTTTTTAC | 2074 |
rs375221680 | snp | C/T | 6.73548e-05 | 0.00580283 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471163 | AAAACAATGTGTAGC[C/T]CTACCTAAAAATTCA | 2074 |
rs375229206 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477605 | TTCCGATGCCCAGGT[C/G]TTCACTTCTGTTCAT | 2074 |
rs375239242 | snp | A/C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529229 | TTCAACTTCAAATAC[A/C/G]AGTGTGGGACAAGGG | 2074 |
rs375265695 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526660 | AGTATTTTGCTTCCT[A/G]TTAAGCCTTAGGTCT | 2074 |
rs375294530 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484292 | TCAAAAAAAAAAAAA[-/G]AAAAAAAAAAAAAGA | 2074 |
rs375330165 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49532109 | CTAAAAATGCAAATC[C/T]GAAAAATTGCCCAAG | 2074 |
rs375342009 | snp | C/T | 6.61846e-05 | 0.00575221 | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524260 | CAGGTCCGCCTCTGC[C/T]CCCTCCACCTCGTCA | 2074 |
rs375358678 | snp | C/T | 0.000153988 | 0.00877328 | missense | ERCC6 | GRCh38.p7 | 10:49461380 | GTGCACCAGAAATCC[C/T]CCTGTGGCCAGTCCA | 2074 |
rs375396715 | snp | A/T | 1.65979e-05 | 0.00288074 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516323 | AAAGCTGAAATATGT[A/T]TCATTTGGAACAAAT | 2074 |
rs375435568 | in-del | -/AGT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526943 | TAACCAGGGAGAGGC[-/AGT]AGAACAAGAAGAGGG | 2074 |
rs375439634 | snp | C/T | 1.66452e-05 | 0.00288484 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482893 | GAAGCACCTTTTTAT[C/T]AAATTTACCTTTTAG | 2074 |
rs375451098 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458361 | AATATAAATGTTTAA[A/G]GTTTAAGCATCAAAA | 2074 |
rs375458461 | snp | C/T | 1.69075e-05 | 0.00290748 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482671 | TGCCAAAAGTATTAT[C/T]ATCCTAATATTTTAC | 2074 |
rs375530418 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503105 | ACTCCTACACCACAC[C/T]GCCTCCATCCTACAT | 2074 |
rs375568706 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479373 | AATGTTCTTAAAGAA[C/T]GCTAAAAATACCTCA | 2074 |
rs375602505 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507730 | TTAGAACTGTGGAAG[A/G]AGTCGGGAGGATATA | 2074 |
rs375610479 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455656 | CATTGGAATAACTGC[C/T]TTTTTGTTTTTGTTT | 2074 |
rs375617750 | snp | C/G/T | 0.00016755 | 0.00915145 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476314 | GCAAAATAAGACCTA[C/G/T]GGACGGGAAAAACAA | 2074 |
rs375621750 | snp | C/T | 6.60769e-05 | 0.00574753 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500499 | TGATGAAATATTAAT[C/T]GAGCTCCACAGACTG | 2074 |
rs375628281 | snp | C/G | 0.000153988 | 0.00877328 | missense | ERCC6 | GRCh38.p7 | 10:49470586 | GAACATTCCCCATTT[C/G]CACTAATCACTGACA | 2074 |
rs375669224 | snp | A/T | | | missense | ERCC6 | GRCh38.p7 | 10:49473480 | TTCACATGTTACCTC[A/T]TTGTATCTCGTAATC | 2074 |
rs375672400 | snp | A/G | | | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454371 | GGACAGGGAGCTGAG[A/G]GAGACGGAGCTCTGT | 2074 |
rs375692468 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489177 | GTCTAGATGATCTTG[A/G]ATGACCATGAACATT | 2074 |
rs375698110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519069 | CAGGTCTTCTAGACT[C/T]CTGAGCCATCTCCCT | 2074 |
rs375699479 | snp | C/T | 0.000115307 | 0.00759211 | missense | ERCC6 | GRCh38.p7 | 10:49532670 | CGTCCTGGTCATAGA[C/T]GTCCACACCCAAACC | 2074 |
rs375732850 | snp | A/G | 1.64795e-05 | 0.00287045 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516764 | TTGTACAGTTAGGTC[A/G]GCTTTTTTCCATTTG | 2074 |
rs375734146 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458374 | AAAGTTTAAGCATCA[A/G]AATAATGCTGTTATC | 2074 |
rs375810438 | snp | A/C/G | 8.28027e-05 | 0.00643386 | ERCC6 | 10 | allele_origin=G(germline)/C(germline) | 10:49474207 | GAGATCAGGGTGGTT[A/C/G]CAAATTTTTCTTAGG | 2074 |
rs375878979 | snp | C/T | 3.303e-05 | 0.00406373 | missense | ERCC6 | GRCh38.p7 | 10:49461430 | GCTCCCAGACACCGC[C/T]GACGAGAGAGCCTCA | 2074 |
rs375921453 | snp | A/G | 9.8868e-05 | 0.00703024 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459154 | GGAAGCGAGGGGCCC[A/G]GATGAAGAGTCTGCA | 2074 |
rs375927208 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526135 | TATATATATATATAT[A/T]TATATATATATATAT | 2074 |
rs375995821 | snp | A/G | 4.94279e-05 | 0.00497107 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524040 | AGACCGACCTTAACC[A/G]CTGCTTATAATAATC | 2074 |
rs376028937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464623 | AAAAAGTGGTTTCAC[A/G]GGCCTGGCCCATGGT | 2074 |
rs376040533 | snp | A/C/T | 4.94319e-05 | 0.00497127 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524192 | GGCACTTTCTTCTGC[A/C/T]GTTTCCCGCCCTTGG | 2074 |
rs376250875 | snp | C/T | 3.30017e-05 | 0.00406199 | missense | ERCC6 | GRCh38.p7 | 10:49493145 | TAGGAACCGGTTTCA[C/T]GTAGAATTGCCACTC | 2074 |
rs376259244 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469055 | AGAGAGAAGGAAAAC[C/G]TTCCTTACAATAGAA | 2074 |
rs376275128 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465175 | ACCTCTTGCATCAGC[A/G]TGACCTGGATGCGAG | 2074 |
rs376280648 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491854 | AAGAGATGTTAACAG[A/G]TAACAGAAATGAAAA | 2074 |
rs376294251 | snp | A/T | | | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454270 | ATTATAGTTTTTAAC[A/T]TCATGAATTTAGCTC | 2074 |
rs376330926 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508228 | AAACACCAGAATATA[C/T]TGCCTTTTGAAGTTT | 2074 |
rs376340387 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534061 | ATCACTTGAACCCAG[A/G]AGGCGGAGGTTGCAG | 2074 |
rs376362412 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491397 | AAGGAAACTGTAATG[C/T]TGTTTTTCCTCAAAA | 2074 |
rs376389083 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501194 | CACTTGGTGATCATA[C/T]TATCTTTTAATAGAA | 2074 |
rs376427825 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473631 | CAAAGCAAATACACA[C/T]TCCCAGTGAGTGCTT | 2074 |
rs376428170 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473432 | AGTCCTTTCCCTCCA[C/T]GTACAGCAGCACCAC | 2074 |
rs376438184 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502048 | CCCACCTTAAAAGAA[G/T]ATAGTTTTGTTGTTT | 2074 |
rs376445140 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474577 | ATAAAAAAGGAATTC[A/G]CCTTTTAAATATGGA | 2074 |
rs376525300 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486861 | TTCCAATCATTGTTA[C/T]AAGGCTAGCAAACCC | 2074 |
rs376526037 | snp | A/G | 4.94482e-05 | 0.00497209 | stop-gained | ERCC6 | GRCh38.p7 | 10:49483504 | AATGAGCAACATCTC[A/G]AATTAGTTTCTCCTG | 2074 |
rs376559145 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465459 | TGAAATGAGTTGAGA[C/G]TTTAGGGGACTGTTG | 2074 |
rs376562265 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512796 | TTTTGTGCATGAAAC[A/G]AAGTTTTGACTGTGT | 2074 |
rs376572844 | snp | C/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540455 | GCTTGAAAGTAAAAG[C/T]AGATATATAGTGGAT | 2074 |
rs376583550 | snp | A/G | 0.000132255 | 0.00813082 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474006 | ACCAGCCTGTTTCCC[A/G]TCTGAAGTCTGTGCA | 2074 |
rs376628378 | in-del | -/CTCT | | | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49515095 | AGAAGGCAATGTGCT[-/CTCT]AAGAAAACATCTTTA | 2074 |
rs376660736 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516646 | AGTACTTGACAATGA[A/G]TTCAATGACCTCGTC | 2074 |
rs376674618 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526258 | GTTCCAACTGGTGTA[A/T]ATTCTTGCCATTCCA | 2074 |
rs376710852 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508714 | GAGATTCTTCTGTTA[C/T]ATAAGCAATACTTCC | 2074 |
rs376744371 | snp | A/T | 4.9458e-05 | 0.00497258 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49524009 | GCAAACAGTACAATG[A/T]ATTTATAATCCCCAC | 2074 |
rs376752542 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481360 | AAAAAGAATGGTATA[-/A]CAGGAGATTCAGAGA | 2074 |
rs376761987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521155 | ACATGCATTGTTGAC[A/G]TGAAAGCAAAGATAA | 2074 |
rs376763121 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534971 | CAGGTCAGCTAGCCC[A/G]GGACACGGACAAGAG | 2074 |
rs376767068 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499344 | GATCTGCTAACTTAA[C/T]GAAAGAGTAAGAAAT | 2074 |
rs376818162 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487963 | CTATTTGTTATCACC[C/T]GATTCAATCGCAGAA | 2074 |
rs376840669 | snp | C/T | 6.59826e-05 | 0.00574343 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478505 | GGGAACATTACTATA[C/T]ATGTTTAAGGAACGC | 2074 |
rs376890272 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498004 | AAAGTCAATTTATTT[C/T]CTTTTCATTATAAGA | 2074 |
rs377033583 | snp | C/T | 3.29495e-05 | 0.00405877 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49530756 | TACAGAATCTAGTTT[C/T]CTGTTGATGTCTCTG | 2074 |
rs377041857 | snp | C/T | 6.58946e-05 | 0.0057396 | missense | ERCC6 | GRCh38.p7 | 10:49470317 | TTCCTTCAAACTTGG[C/T]GTCTCTGCAATGCTT | 2074 |
rs377050453 | snp | C/T | 3.32055e-05 | 0.00407451 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460363 | AAAGCAAAAAGGTTA[C/T]CTATATTACCTGGCA | 2074 |
rs377077047 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499986 | AACTTCATTCAAAAA[A/C]AAGAGAGAGAGCAAG | 2074 |
rs377083846 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504695 | GCCTTTATTTACCTT[C/T]CCATAGTTAATTCTC | 2074 |
rs377103568 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467060 | TGCTGGGATTACAGG[C/T]GTGAGCCAAGCCCCA | 2074 |
rs377124191 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487483 | TAAAAACACACGTAC[A/G]GGTTCCCTCAGGACT | 2074 |
rs377170944 | snp | A/C/T | 1.64779e-05 | 0.00287031 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515690 | CTTTCCACGGATTGA[A/C/T]GCCCGATACTTATCA | 2074 |
rs377238628 | snp | A/C | 5.11261e-05 | 0.00505573 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476166 | TCTTTTCCTCCCTCA[A/C]TTCTCTTGGTCCACA | 2074 |
rs377246446 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522759 | GAAAAAGTCTGACAC[C/T]GCTCACTGTTCAAGA | 2074 |
rs377278906 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464502 | ATTTGCATTACGTAA[C/G/T]GAGGAGCCAAATGTT | 2074 |
rs377326746 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531184 | TTTACATGAAAAAAT[A/G]CATACATGGGTTTTT | 2074 |
rs377342567 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467975 | AGCAGTGCTCACTCT[-/A]AGGCTGATCATTCCC | 2074 |
rs377344809 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502215 | TGCAAAGCAATTCTA[A/G]AAGTTTGACTCTAGC | 2074 |
rs377357172 | snp | A/C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524237 | TCATAGTCAGTACCA[A/C/T]CTCCAGACAGGTCCG | 2074 |
rs377373795 | snp | G/T | 1.65228e-05 | 0.00287422 | missense | ERCC6 | GRCh38.p7 | 10:49473021 | AGAAACACAAATATG[G/T]ATGTGTCCTAGAGGT | 2074 |
rs377449778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508420 | CCCTCCTAAAATATA[C/T]AGGCATCTTGTCGCC | 2074 |
rs377454424 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484237 | AGTGAGCAGTGATGG[C/T]ACCACTACACTCCAG | 2074 |
rs377498675 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478507 | GAACATTACTATATA[A/T]GTTTAAGGAACGCAT | 2074 |
rs377509822 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507500 | AAAGGCAATCTCTTC[C/T]TCTCCACTGGTATTT | 2074 |
rs377513917 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494930 | GCCTCCCCCTCTGTA[A/G]GTTTCTAGGTGTACC | 2074 |
rs377545597 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506420 | AAAAATAGATTTATA[A/T]TTACTATTTCTGTTC | 2074 |
rs377579703 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495664 | CAAACCAATGGAAAG[A/C/T]ATTTTGTCCCACTGT | 2074 |
rs377611273 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532764 | CAGGGCTGGCCCTCT[C/T]CTCGGAGCTGCTGAT | 2074 |
rs377615037 | snp | C/T | 3.29554e-05 | 0.00405914 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470603 | ACTAATCACTGACAA[C/T]TCTTCTGGTCCAGAT | 2074 |
rs377628338 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501285 | CATAACAGATGATTC[C/T]GTCATATTACTAGCA | 2074 |
rs377674666 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533833 | TTTTAAAAGATTAAT[A/T]AAAATATTCTCAAAA | 2074 |
rs377693960 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474476 | TACTGGACTGAACAC[A/C/G]TCTACAGGGGTCATA | 2074 |
rs377708438 | snp | A/G | 0.000164747 | 0.0090745 | missense | ERCC6 | GRCh38.p7 | 10:49532613 | CACGGCTGGCCTCAT[A/G]GATGGCATTGTCCAC | 2074 |
rs377708780 | snp | A/G | 4.99979e-05 | 0.00499965 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471129 | GATTTGTCTAAAAAA[A/G]TAAAAGATAAGCTGG | 2074 |
rs377708874 | snp | A/G | 4.99663e-05 | 0.00499806 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493280 | GTCCAAGAAGAAAAC[A/G]ACCATGAAAGAGCAT | 2074 |
rs377711653 | snp | C/T | 1.64961e-05 | 0.00287189 | missense | ERCC6 | GRCh38.p7 | 10:49470469 | CAAAAAGCTTCTGTT[C/T]GAGCCTGGCTGGGTC | 2074 |
rs377759740 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515809 | GTTTCTGGGAGTAAC[A/G]ACTGACAAGACACAG | 2074 |
rs377760574 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472484 | GCCTGCAACAGAGAG[A/G]GAGAGACCTCTCAAC | 2074 |
rs386743577 | in-del | C/TAGAGTCT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484671 | CTTGAGCTCAGGAGT[C/TAGAGTCT]ACAGTGAGCTATAAT | 2074 |
rs386743578 | in-del | AG/TGAAGAAGTTAAT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494409 | AGAAGTTAATAAACT[AG/TGAAGAAGTTAAT]AAAAATGTTCACCAT | 2074 |
rs386743579 | in-del | AA/TAG | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521868 | TTGACGGAAAATTCC[AA/TAG]TAAGTATCAGCTAAA | 2074 |
rs387906262 | in-del | -/A | | | frameshift-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524457 | GTTCTGTCCAAAAAA[-/A]GAGGAGCGTTTGAAA | 2074 |
rs397727875 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490372 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 2074 |
rs397897609 | in-del | -/A | 0.000924886 | 0.0214846 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530879 | ATTTTGCACTCTGAT[-/A]ACATTTTTATAGCAT | 2074 |
rs398013396 | in-del | -/T | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468992 | TGGACTAATGGATTC[-/T]TTTTTTTTCCATGAC | 2074 |
rs398013397 | in-del | -/T | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502960 | CTAATTGCACATCAG[-/T]TTTTTTGGAGAGCTT | 2074 |
rs398075129 | in-del | -/T | | | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454143 | ATTTTTCATTTTTTT[-/T]TCTCTCTGTTCTTTG | 2074 |
rs398075130 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502959 | AAAGCTCTCCAAAAA[-/A]ACTGATGTGCAATTA | 2074 |
rs398114303 | in-del | -/T | | | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454144 | TTTTTCATTTTTTTT[-/T]CTCTCTGTTCTTTGG | 2074 |
rs527236039 | in-del | -/A | 3.29495e-05 | 0.00405877 | ERCC6 | 10 | allele_origin=A(inherited)/+.-----(germline) | 10:49530716 | AAGTATAATAAGGTG[-/A]TTCAGAATAACATTC | 2074 |
rs527253354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500820 | GTCAGAGAAACATGC[A/G]GGATGTGTGTTTTAC | 2074 |
rs527280158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538836 | AGACCCGCTACAGTG[C/T]GTCCTCGCTGACAGG | 2074 |
rs527295952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461167 | AAACAGGGGATGAAA[A/G]CAAGGAGGAAGGCAA | 2074 |
rs527389423 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521962 | GAGAATAAAGAGGAT[A/G]AGATATCCAGAAGTC | 2074 |
rs527404546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501758 | CCCAGGAGTTCAAGA[A/C]CAGCATGGGCAACAT | 2074 |
rs527408313 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493466 | ATCAATTAGTGGATG[C/T]AGGTGTTAAGAGAAA | 2074 |
rs527446982 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467700 | CCTCGCAAGTAGCTG[A/G]GACCACAGGTGTATG | 2074 |
rs527631227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521613 | TTTACTTCTAAGCAG[C/T]GGCTCATCCATCCTG | 2074 |
rs527679768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468386 | CAGCACGAAAATTCT[C/T]TCAAGGCAGTAGGGC | 2074 |
rs527687901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515152 | ATTTTTTGAATTTTT[A/G]CATGAAATTCATATA | 2074 |
rs527688386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522107 | TAACCACTAAAAAAA[A/C]ACTAATTTTCTATGT | 2074 |
rs527784343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510447 | AGCAGACCTTTCAAA[C/T]CCTCACTCATGCAGC | 2074 |
rs527832625 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495017 | AATATCCTGATACGT[C/T]CTACACTGTATTCCC | 2074 |
rs527856019 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456129 | AAACTAATTGCTATA[A/T]TAGACTTCAAAAGAC | 2074 |
rs527907378 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540005 | CAATGTAACTTGTTT[A/T]TGTTGGTGGTAGTGG | 2074 |
rs527944087 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534406 | CACACACAGGTGCAA[A/G]AATGTTTAGTGCAGC | 2074 |
rs527992867 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531443 | CAATCTTCTTGATGA[C/T]TGTGTAATTTGCTGT | 2074 |
rs528006131 | in-del | -/GAGTTA | 0.0158469 | 0.0875917 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484667 | ATCCCTTGAGCTCAG[-/GAGTTA]GAGTCTACAGTGAGC | 2074 |
rs528012690 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495548 | GCCCAGATCACTCTT[C/T]TGAACTCCAAACCAC | 2074 |
rs528052703 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465055 | AGCTTGCACCATGCA[-/C]CTGGAAAGGCTGCAG | 2074 |
rs528081368 | snp | C/T | 0.000345887 | 0.0131462 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524621 | AAATACTTTTCGAAG[C/T]CTGATGCTTCATTAA | 2074 |
rs528103634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518041 | GAGTTGGCCTTTGCC[A/G]AAGCACAGCCTAAAA | 2074 |
rs528126755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465078 | GGCTGCAGACACTCA[A/G]TGCCACCCATGAAAG | 2074 |
rs528187739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505661 | GGTCCATATAGATTC[A/G]TCAGTTTACAAACAT | 2074 |
rs528193106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513036 | ATTTCAAGCATCTTA[C/T]TGCCTTGGTGGAATC | 2074 |
rs528250606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497987 | AAAATTAACTGAGTT[C/T]GAAAGTCAATTTATT | 2074 |
rs528254791 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536224 | ATGGAGGCCACAAGA[A/G]AGTGGCCTGTCCTTT | 2074 |
rs528434501 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509872 | AAAAAATCCACACAC[A/G]TAATAGTCACAGCTG | 2074 |
rs528466340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525366 | TTTTCAAGTGCTCAA[A/G]AGCTACACGTGACTA | 2074 |
rs528506488 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49466809 | ATATATTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 2074 |
rs528526928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492772 | TTCCTAAAACTGTTT[C/G]AAGCCACTAATGCGC | 2074 |
rs528568592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485997 | GATATATCAAAGAAA[C/T]GCCAACCAAAAAAGG | 2074 |
rs528587597 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479077 | GGTTCTGTAATGGAG[C/T]ACGGCCACATGAGAT | 2074 |
rs528641798 | snp | C/G | | | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454330 | ATGCTGGCATCTTGC[C/G]CCTCCCTGTGAGGTA | 2074 |
rs528658179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520477 | AAGAAGAGACAAAAA[C/T]ATATCTGGAAATGCA | 2074 |
rs528665931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466417 | CATGGAAAGGGCCCT[A/G]GGGTGCTGAAATGAA | 2074 |
rs528677167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473301 | CATGCCCACAATCCC[C/T]GCCCCCAAATATCCA | 2074 |
rs528688296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519940 | GCCCAGGCCCCTACC[C/T]TCTGAAGGTGTTTCC | 2074 |
rs528710619 | snp | A/C | 1.82443e-05 | 0.00302024 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472896 | TTCTTTTAAAAAAAA[A/C]ATAAAAACAAACCTG | 2074 |
rs528795243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507515 | TTCTCCACTGGTATT[G/T]TTTTTCCTTAAAAAT | 2074 |
rs528878779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534374 | GCAATTCTAGGTATT[C/T]ATTCCAGAGAACTAG | 2074 |
rs528950816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482473 | TATTCTAGGGCTTTC[C/T]TCTCTGTGAATAGTT | 2074 |
rs528962485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489539 | TAAGCACAAAACCAA[C/T]GCACTTAAAACTGCA | 2074 |
rs529049168 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520521 | GATGCAACCCATCTA[C/T]GCCCTGCAGCCTGAC | 2074 |
rs529053097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523281 | TTCAGTGGGCCACCA[C/T]GGGGAGGCCTGCAAT | 2074 |
rs529115727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475742 | CCAGGGACATTTGAA[A/C]CAGATTTATATCTGG | 2074 |
rs529154666 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463223 | CACACATAGCCTGAA[G/T]GTAATTTTAATATAA | 2074 |
rs529174213 | snp | A/G | 1.64743e-05 | 0.00287 | stop-gained | ERCC6 | GRCh38.p7 | 10:49470299 | CCAGGTGTGGAATTC[A/G]AGTTCCTTCAAACTT | 2074 |
rs529182862 | snp | C/T | 1.658e-05 | 0.00287919 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476210 | GCTTCTATTTTTTAG[C/T]TGACCTGCATCTCTC | 2074 |
rs529183152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517206 | TGAAAAATGTCAAAC[C/G]CATAACTAATGCAAT | 2074 |
rs529187280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510561 | GGACACACCTGGGAT[C/T]TCTACTACAGTGCCC | 2074 |
rs529196262 | snp | A/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518617 | CCCTAAAGGCTGCAA[A/C]GTTCCAAATCCACAA | 2074 |
rs529199458 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513778 | CCTTGACATATGGGG[-/A]ACTACAATTCAAGAT | 2074 |
rs529229202 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496822 | TCAGAACAAACAAAC[A/G]AACAAACAAAATACA | 2074 |
rs529266424 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522802 | ATTCCTCAAACAACT[G/T]CACAGGTAATAAACG | 2074 |
rs529340391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463845 | CCTTCTGACATGACT[A/G]TGAGGCCTCCACAGC | 2074 |
rs529352971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497143 | GAGTTTCTAAGCCAT[A/G]CTCCTCACCAAGGCA | 2074 |
rs529389886 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504501 | GCAGACTCAACTTGA[A/T]CCTTGAGGATATCTG | 2074 |
rs529409360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496345 | CAAATGATCTCAATG[A/C]CTACCTAATAGCAAG | 2074 |
rs529419098 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496335 | ATCTCTTCTTCAAAT[A/G]ATCTCAATGCCTACC | 2074 |
rs529475007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530238 | AAAAAGGAACTTTTC[A/T]CAAATACACAGATGG | 2074 |
rs529616195 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507482 | TTTTTGTGCTTAACT[G/T]CTAAAGGCAATCTCT | 2074 |
rs529616761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483848 | CAATGTGGATGGAAA[A/C]TATATTAATTTAAAA | 2074 |
rs529699821 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538263 | ACAGTTCTGAGAGGG[C/G]ACAGGCAAGGGCCAA | 2074 |
rs529752476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461092 | TCCTGTATCTCTTAC[C/T]ATTTTTAACAACACC | 2074 |
rs529770968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499923 | TTAGAATTTATTACA[C/T]AAAGTTCATAGATTG | 2074 |
rs529790488 | in-del | -/T | 0.289942 | 0.246789 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526316 | GTACCACATTATGGC[-/T]TATAATTTACATTTC | 2074 |
rs529795031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492895 | TGGACAACAGACATT[A/G]TCACAACACCACCAC | 2074 |
rs529827067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507897 | TATAGGTATCCCTTA[C/T]TATCAAAACTTAGAA | 2074 |
rs529921980 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467808 | TCCTAGGCTCAAGCA[A/G]TCAACCCACCTCAGC | 2074 |
rs529929528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480593 | AAAAACAGATCATAA[C/T]GACATGTTCTCAAAT | 2074 |
rs529998290 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487850 | ATGATTAACAAGAAT[G/T]AAAAAGATGCTTATG | 2074 |
rs530035963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486919 | ATGAGTGTGCATACA[C/T]GCCTCTAAACTAGAG | 2074 |
rs530119828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527435 | ATCCCAGTACTTTGG[C/G]AGGCCAAGGTGAGCA | 2074 |
rs530124462 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520787 | CCTCCCTGTCCTCAG[C/T]CTCTCTGCACATTGT | 2074 |
rs530133767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508735 | CAATACTTCCTCATG[C/T]GACTTGTAGCCAAAA | 2074 |
rs530154728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481248 | AATCAGTGAATCTGG[A/G]TGAAGTGTTAAGAAG | 2074 |
rs530192637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501953 | CAACAGAGTGAGACC[C/T]CATCTCTAATAAATA | 2074 |
rs530214510 | snp | C/T | 3.29647e-05 | 0.00405971 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515750 | CATGAACTGGTTATA[C/T]ACTTTGATCATGTTT | 2074 |
rs530231773 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454804 | ATTATGATACCACAA[C/T]GATAAAAACAGTGGG | 2074 |
rs530249726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49515037 | GTGTGCAGAGCAGGA[A/G]GCAGAATTAGTCTTC | 2074 |
rs530267021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468328 | TGCCTTTTCAACAGA[G/T]GGTCTGCCTGGACTC | 2074 |
rs530284059 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504374 | TATTATTTATATTAA[C/G]TACTATAGAGTTTTG | 2074 |
rs530376362 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539869 | ACTGCGGGTCACTGC[C/T]TGGGAAGTGCTGTCC | 2074 |
rs530378272 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455502 | ATGGCAAAACACAAT[A/G]CAAAGCACCAAATGA | 2074 |
rs530405215 | snp | A/G | | | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454312 | AGCTGGAGGGGATAA[A/G]AAATGCTGGCATCTT | 2074 |
rs530434892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530146 | GGAGACTGAGGCCAG[C/T]GTGACCCTAAGCCAG | 2074 |
rs530467765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476491 | TACCCTGCTCACCAG[C/T]CCCTCCATCTCTGTC | 2074 |
rs530496635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523955 | ATTAAGCTGGATCTA[A/G]AATGCTTACATATTA | 2074 |
rs530497515 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526440 | TTTGTCTGTTTCTTT[-/A]AATGATTTCTAGTTC | 2074 |
rs530604017 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477230 | CAGGATCAGGCATGA[C/G/T]TCCCTGGTTTTCACT | 2074 |
rs530611814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465042 | TAGATCCACTGACAG[C/T]TTGCACCATGCACCT | 2074 |
rs530639675 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506811 | TTGTCGTGAGTGGGG[-/A]AAAAAAAAAAGCCTC | 2074 |
rs530654631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471577 | CAGGTCCACACTCTG[C/T]TGAAGCCCCACACCA | 2074 |
rs530664307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517920 | TATTTAGGTTTCTGG[A/G]TAAAATCTCAAACTT | 2074 |
rs530673596 | snp | C/G | 0.000856235 | 0.0206733 | missense | ERCC6 | GRCh38.p7 | 10:49458982 | GGCCATCAGTGTGGG[C/G]CTGGAAAGCGATGAA | 2074 |
rs530699457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504668 | AAACAAAAAGAGTTG[C/G]CAATAAAAGTGGCCT | 2074 |
rs530727101 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458316 | CAAACAACAAATAAC[A/G]AACCTGACCTTTGTG | 2074 |
rs530744532 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505575 | AGTTTGGCACCTTAA[A/G]ATTACTAAGAACAAA | 2074 |
rs530759566 | in-del | -/TTAA | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463449 | AGGAATAGCTCTCTG[-/TTAA]TTAATACTGCAGTGG | 2074 |
rs530908256 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49483639 | CATGCACAATCACAG[A/G]CATTATCAGCACTGG | 2074 |
rs530915529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537379 | GAAAGAAATCATACA[C/T]TTAACAAATAGTTAC | 2074 |
rs530957881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536739 | ATCTCCAGGGCTGAA[C/T]AATCTCCTCCTTCAG | 2074 |
rs530980379 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519519 | AGGAACCAACTCAAA[A/T]CCACTTCAGGCTATG | 2074 |
rs531055352 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478974 | ATAAGCAGAGATTAC[C/T]GTCCACTGGAGACTT | 2074 |
rs531091147 | snp | C/T | 1.65493e-05 | 0.00287652 | missense | ERCC6 | GRCh38.p7 | 10:49482692 | AATATTTTACCTGTA[C/T]TGGGGAAGCATTTGA | 2074 |
rs531104994 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513656 | TGAGTGCAAGCACAG[A/G]AAAAACTTCCACTTT | 2074 |
rs531107283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525893 | TCTCTGAACGCTACG[C/T]AAGTGGAAATGTTTG | 2074 |
rs531214416 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476801 | ACCACTCCATGCGAT[C/T]GTGCTCTGTGACCCT | 2074 |
rs531234367 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539299 | AAAAATACCCTGCTG[A/G]CAAGGCAGTTATGAA | 2074 |
rs531242343 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479722 | GCAGAAGAGCGAGCA[C/T]GCTGGTTGGAGGTGC | 2074 |
rs531320399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494724 | TGACCAACTTTGTAA[C/G]GAAAAATTACATTCT | 2074 |
rs531329516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488070 | AGACAAATCATCTCG[C/G]GCGGTTTCAAATTAA | 2074 |
rs531340817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523159 | GAAAAAGCCATCCCA[C/T]TATCAAGTATTTTAA | 2074 |
rs531377254 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492624 | ACTGTCAATACATGA[C/T]GATCAAGGATTCAAG | 2074 |
rs531387042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533756 | TGCAGTGAGCCATGA[C/T]TGCACAACTGCACTC | 2074 |
rs531416571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528191 | ATAATAAATGTGTAC[C/T]AGCAGCCTCCTATGA | 2074 |
rs531488984 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526153 | TATATATATATATAT[A/T]TATATATATCTGGGT | 2074 |
rs531508840 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461755 | ACACACAGAAACCTA[C/T]AACCTTCCTATTTAC | 2074 |
rs531517895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482421 | TCCCAGGAACAATGC[A/C]AAAACTGTTTAATTT | 2074 |
rs531562463 | snp | A/C | | | missense | ERCC6 | GRCh38.p7 | 10:49470637 | GCATTTGTCTCTTCT[A/C]CAAGCCTATCATTGC | 2074 |
rs531648623 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475056 | TAAGTCAGGAACATT[C/G]GTAAACCTCCCCAGA | 2074 |
rs531654713 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540753 | TGAAGATAGGGTCTT[A/T]AATGAGGGAATTTAG | 2074 |
rs531699603 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510517 | AGGTGTCCTGTCTTC[C/T]AAGGGCCCTCCCAAT | 2074 |
rs531735337 | snp | A/G | 1.65392e-05 | 0.00287564 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516565 | GAAAAATAATTCCCA[A/G]AAAACATTTGAATTC | 2074 |
rs531744273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511107 | ATTTAAGTCTGAGCT[C/T]CATTTTTTGGGTTCA | 2074 |
rs531774879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469447 | AAATGTTAATAACTT[A/C]GATAAAGGATATAGG | 2074 |
rs531827955 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463897 | TAAACCTCTTTCTTT[C/T]GTAAATTGCCCAGTC | 2074 |
rs531831972 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456862 | ACAATGTGTCAGATC[C/T]CCACACTGAGACACC | 2074 |
rs531832928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503780 | AAAAATTACTCTTTA[A/G]GGACAGTTAAAGATT | 2074 |
rs531895328 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490905 | AAGAAATCACAGCTG[A/C]TAAGGAAGTCAGGCA | 2074 |
rs532002241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465567 | TGTCCCAGCCAAATC[G/T]CATCTTGAATTGTAA | 2074 |
rs532012333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519476 | CAGAAGTGCTGAAAG[A/G]TGGCGAGGGAGCCTT | 2074 |
rs532032860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459662 | CATAGCTATACTTCC[A/T]TTTCTTCACTTTTAA | 2074 |
rs532053632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490313 | GATAGATGTGCTTAA[C/T]TGAGAAATTGACCAT | 2074 |
rs532131078 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481955 | CTGTAGCCTGAGGAA[-/C]CCCTGAGAACCAGCA | 2074 |
rs532134477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512742 | TTTATGTTTCATATA[C/T]AACTTATACACATAG | 2074 |
rs532147748 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498493 | CCGCCCTGGTACATA[G/T]GAGCGGGGGGGACCA | 2074 |
rs532161226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465159 | AAGACCATAGGAACC[C/T]ACCTCTTGCATCAGC | 2074 |
rs532196671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538197 | CATCACTGGGGCTCC[C/T]GCAGCCAGGGGCAAG | 2074 |
rs532236039 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507437 | CAACAGTTTAATAAG[A/T]GATACTTTTTATAAA | 2074 |
rs532259992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513555 | GTTTAATTGACTCAC[A/T]ATTCGGCACGGCTGG | 2074 |
rs532264215 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | ERCC6 | GRCh38.p7 | 10:49539499 | GGAAGGATGGAGAGC[C/T]GTCCTGCTTCTCTGT | 2074 |
rs532273214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506508 | TGGGGTCAAAATCAC[C/T]GAATCAGGTTCACAT | 2074 |
rs532290721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486171 | GCCCTTAGAGCTGTC[A/C]AAATGACACATCCAC | 2074 |
rs532298256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499797 | TAGATTAAATGCTTA[C/T]TCTTCTGGAATACAA | 2074 |
rs532327278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492837 | TATGACTCCAACCCA[C/T]ACTGCCAGGCTTGTG | 2074 |
rs532339913 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536321 | GGAGAGAACTAGGGC[A/C]AGAAAAACTAGAGCA | 2074 |
rs532361003 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537500 | AACTATATATATATA[C/T]ATACACATACACACA | 2074 |
rs532443504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473413 | TAAGGGTGTGGATAC[A/G]CTTAGTCCTTTCCCT | 2074 |
rs532475692 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534143 | ATCTCAAAAAAAAAA[-/C]AAAAAAAAAAACAAA | 2074 |
rs532526370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526646 | AGGTCTTTACACTGA[C/G]TATTTTGCTTCCTAT | 2074 |
rs532530772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520097 | TTTGAGAAACTGATA[A/T]ACAAACTGCATCAGC | 2074 |
rs532601635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514387 | ACTGCCCATACCAAC[A/G]CACAAAAGGGACAAA | 2074 |
rs532630883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467186 | TAATAAAGCTGCTAC[A/G]AATATTCATGTACAA | 2074 |
rs532696862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520499 | GGAAATGCATTTTCT[C/T]ACTCAGGATGCAACC | 2074 |
rs532706262 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509346 | TTACTATGTTCACTG[A/G]AAGAAGAGAAAGCAA | 2074 |
rs532771727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522846 | AAGCTGTGCTGAGGG[A/G]TGACAAATATAAGCC | 2074 |
rs532799236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461766 | CCTATAACCTTCCTA[C/T]TTACAAACAATAGCC | 2074 |
rs532937848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529573 | CTGCTAGCTTTGACC[C/T]TTGGGCTGCTATTCT | 2074 |
rs532948706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517841 | GAGCCATTGTGCCCG[A/G]CCAGGCTTATTTCTT | 2074 |
rs533085189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511931 | GTTGAATCTGCCTCC[C/T]CCACCACAAAATGAG | 2074 |
rs533090507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523481 | GTATGCTGTGCATAC[A/G]AAGTACACTTTTTGC | 2074 |
rs533122882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514815 | GTTTTCTATTTCAGA[C/G]AGCTAAGAATGCCTT | 2074 |
rs533142472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463890 | AGTTGATTAAACCTC[C/T]TTCTTTTGTAAATTG | 2074 |
rs533205380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530268 | GTCTCCAACTTATCA[C/T]GGTCTGACTTGCAAT | 2074 |
rs533222802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536510 | GGAAAGGAGGGAAGC[G/T]GAAGTGGATTACAGA | 2074 |
rs533246538 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486504 | ACTCTTTGGAAAGAC[G/T]AAACCAAACAAACCT | 2074 |
rs533264005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497777 | CTACAATTCCTTTAA[C/T]CTTTGATTACCATTG | 2074 |
rs533303920 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501518 | TCTCCATCAATGATA[C/T]GTTTAATCTATAACC | 2074 |
rs533325137 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524656 | GATTTTTCTGGGCTT[C/T]TTCTCCTGTTTCTGA | 2074 |
rs533351609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536154 | GGAGCGATAGGGCCA[A/T]AAACCAGACTGTAGT | 2074 |
rs533383172 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458051 | GTGCATGCATGTGTG[C/T]GGTTTTTATGTACCT | 2074 |
rs533405714 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454289 | TGAATTTAGCTCTTG[C/T]CACTTGAAGCTGGAG | 2074 |
rs533441805 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518280 | GTGGAGGGAGAAACC[A/G]GGCACTGAAACAATG | 2074 |
rs533452156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484019 | TACAGTGGCTCACAA[C/T]TGTAATCCCAGCACT | 2074 |
rs533512790 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490926 | AAGTCAGGCATTAGA[C/T]GCTGAGTTAGAGGAC | 2074 |
rs533536820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532167 | AGCTAGAAAGAAGCT[A/G]CCGCACAGAGAAAAA | 2074 |
rs533608565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511779 | TCCAGTGGTGGTCAC[C/T]AGAAGAGAACCCAAC | 2074 |
rs533616116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484475 | CCAGGCAAAGTGGCT[C/T]ATGTCTGTAATCTCA | 2074 |
rs533630825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478822 | GGTTCTTGACCACCA[A/G]CCCTAGGGGAAAAAC | 2074 |
rs533644384 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529893 | CTTAAAAAAAGTTTC[A/C]AACTTCATAAAAATA | 2074 |
rs533646206 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488747 | TTTAAAGAACATGTT[A/G]ATGGGAGTTTCATCG | 2074 |
rs533649368 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471788 | GTAAAGGGCACAGAG[C/T]TTCCTATAAAAGCTG | 2074 |
rs533677342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478183 | GAGGGAGGTCAAAGC[C/T]TGTGGACTAGAGAAG | 2074 |
rs533680447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484940 | TGACCATGGATTCTA[C/T]ATCAATCCAAACTAG | 2074 |
rs533813681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538327 | TTCCACTCCCAGTGC[A/G]ATGGAATGACTCTGA | 2074 |
rs533886138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486538 | AAAAGTGAGCCAAAA[C/T]AACAGACTGAGATGT | 2074 |
rs533904647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501435 | TTTAAATAAGGAATA[C/T]GGGTCAAAGAGAAAT | 2074 |
rs533923786 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454196 | ATCTGCCAGTTGGCT[A/G]ACAATTTCTTCTGCC | 2074 |
rs533950776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513950 | TTCAAACCCAGATAA[C/T]CAAGTTCCAGAGTCT | 2074 |
rs533984667 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454894 | TCCGTACATTATATG[C/T]AAATTGGTAAAGGTG | 2074 |
rs534018647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480632 | TATAAATGACTTATT[A/G]ATGCCAAAGGAGAAG | 2074 |
rs534061087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467319 | TCCAAAGTGATTGTG[C/T]CATTTTACATTCCCA | 2074 |
rs534069891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493878 | AGCACCATGGAGGAG[C/T]ATCCGAGCGAGTGTT | 2074 |
rs534095433 | snp | C/T | 0.000164728 | 0.00907398 | missense | ERCC6 | GRCh38.p7 | 10:49473569 | GGGCTCTAAGGAATA[C/T]TTCAAGTATGTCCAG | 2074 |
rs534168918 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472720 | ATGAATGCTATGGAT[-/A]AACTGCTGAAGATGG | 2074 |
rs534177962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521858 | TGGAAAGGGCTTGAC[A/G]GAAAATTCCTAGTAA | 2074 |
rs534184569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508393 | ACAAGATTCAGTTTC[A/C]TCCTCCTCCCTCCCT | 2074 |
rs534198797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482025 | CCTCCCTGAGTGCCA[A/C]TGCTTCCCTTTCAAG | 2074 |
rs534237805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488942 | GGTGCCTGCCACCAC[A/G]CCTGGCTAATTTTTT | 2074 |
rs534299486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494319 | GTAAAGTGCTTAGAA[C/T]AGGACCATATAGAAA | 2074 |
rs534307651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464631 | GTTTCACGGGCCTGG[C/T]CCATGGTCCCCATGC | 2074 |
rs534312952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502008 | GCATTTTTTTTTCAA[A/G]GAAAATATCAAGGCT | 2074 |
rs534342516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464155 | GTGATATGAACAGTA[A/T]GGTCCAAACTGAGGT | 2074 |
rs534363928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488375 | CTAGGCAGGATTTAC[C/T]GCACCTGTAATTAAT | 2074 |
rs534382102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533962 | AACATGGTGAAACCC[A/G]ATCTCTACTAAAAAT | 2074 |
rs534418074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497463 | AAACTGCTACATTGA[C/T]GACTCACATTTTGTT | 2074 |
rs534456904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504791 | TTCTACACGGCTGTT[C/T]CTCTGTCCAGTTAAA | 2074 |
rs534463582 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491376 | TAAGAGTTTGAGTAA[A/C]AACACAAGGAAACTG | 2074 |
rs534541140 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500480 | TCCTCCACAGCAATA[C/T]ATCTGATGAAATATT | 2074 |
rs534617515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491917 | AGGATAGTTTAAGGT[C/T]TGACAAACAATTTAA | 2074 |
rs534670354 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478225 | GGCAGACGCCACAGC[A/G]GGCCTAGCCTGCCCA | 2074 |
rs534686960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519129 | GCTTAGGTTTTTGGT[C/T]TGGTTTTCAGTCCAA | 2074 |
rs534697990 | in-del | -/AC | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527847 | CCACCAACAATTTGT[-/AC]ACACACACACACACA | 2074 |
rs534803517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537074 | ACATTTGCCGGGAGC[A/G]GTGGCTCATGCCTGT | 2074 |
rs534807683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471919 | ATTATGGAAAGACAG[A/G]GGACGAAACAGCCAT | 2074 |
rs534829153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512862 | AATTTTCCACTTGTG[A/G]CATCACGTTGCTAAA | 2074 |
rs534845108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536297 | TAATAATGGATTTGT[C/T]GGGGGTAGGGAGAGA | 2074 |
rs534893443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477593 | ACCCTACTCACCTTC[C/T]GATGCCCAGGTCTTC | 2074 |
rs534994904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492566 | ACAGATAAAGCTCTT[C/T]TTTGATACTGTGATA | 2074 |
rs535080698 | snp | A/G | 3.31318e-05 | 0.00406999 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472514 | CGAGAATCCTTCCCA[A/G]TGACAAGCACTGACT | 2074 |
rs535164301 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538006 | CGTAACTTTTAAGAC[C/T]AGAAAGAGCTGATGC | 2074 |
rs535169579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475142 | ACTAGTCACACGTGG[C/T]TACTGAGCACATGAA | 2074 |
rs535176880 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523215 | GACTTCCTTAGAGCT[-/A]AAGTGAGCTCTAAGT | 2074 |
rs535219338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460108 | GGCTGTCCTAGCAGC[A/G]ACACACCTATCCCTG | 2074 |
rs535220065 | snp | C/T | 1.75937e-05 | 0.0029659 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515336 | TGGTGACACCTGCTA[C/T]TCAGTGTGATATTCA | 2074 |
rs535242154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522241 | CAATTAGTCTACAAA[A/G]ATCAGCAATGAGTAA | 2074 |
rs535262972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465722 | AAATGGGAATTTCTC[C/T]GCACAAGCTCTTTGC | 2074 |
rs535278803 | snp | A/G | 3.31559e-05 | 0.00407147 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516039 | AGCTTATCAAGAAGT[A/G]CAATACTGGTGAAAA | 2074 |
rs535303380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509046 | GCAGGCCCAGGCACA[A/G]AAGTCTGAGCTCAGA | 2074 |
rs535327000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499995 | CAAAAACAAGAGAGA[C/G]AGCAAGCTATCTAGA | 2074 |
rs535332775 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540248 | TTCGTCATGTTAGCC[A/C]AGCTGTCCGCGAACT | 2074 |
rs535384193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503336 | AAATCTAATCTTCGA[C/T]GGCTTTCAAACAGCA | 2074 |
rs535441217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495813 | TGTCTCTCCGTCTAC[A/G]CTGTTGCTATGCCAG | 2074 |
rs535487854 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534154 | AAAAAAAAAAAAAAA[A/C]CAAAAAAAAAACTCC | 2074 |
rs535495750 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456275 | GATGCCAGGTCACTA[A/C]TGAAGCTCCCATTGG | 2074 |
rs535542084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474497 | AGGGGTCATATTCAA[C/T]TGCTGATAATTCATT | 2074 |
rs535553112 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491327 | TTTAGTGATCTAAGA[G/T]ACTTTATAATGGAAA | 2074 |
rs535566582 | in-del | -/AC | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486540 | AAGTGAGCCAAAATA[-/AC]AGACTGAGATGTACA | 2074 |
rs535616736 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456086 | AAGGATGGTATAAGG[C/T]CATTAATATAAATTA | 2074 |
rs535635812 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462499 | ACTGACAATTTTTTT[A/T]AAAAAAAACCTGTTT | 2074 |
rs535655402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523721 | ATTCTAGGGTGACTG[A/T]CGGTATAAAGGCGAC | 2074 |
rs535674253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462124 | AAAGTAACACCCTAT[G/T]GGACAATAAAACACG | 2074 |
rs535688319 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489560 | TAAAACTGCATGCTC[C/T]TGTTGCTTTTCCCAC | 2074 |
rs535735727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462417 | AAGTAGTACAAGAAA[A/G]CATGGCGAATTATCA | 2074 |
rs535742997 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482079 | GCTTTTTAGCTATGC[C/T]CCCACAAGCATCTCC | 2074 |
rs535817476 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464630 | GGTTTCACGGGCCTG[A/G]CCCATGGTCCCCATG | 2074 |
rs535841271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537780 | GAGTGCAACCTCCGC[C/T]AGGCTCCGCCAGGCT | 2074 |
rs535893168 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537128 | AGGCGGGAGGATCAC[A/C/G]AGGTCAGAAGTTCGA | 2074 |
rs535898220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529192 | TGTGGTACCTGGTTC[A/C]TCTTTCCAAGGTCAA | 2074 |
rs535929212 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482837 | CATCGGTGAGCCAGA[C/T]AGAATGATCCGATGA | 2074 |
rs535936907 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491642 | ATGAGTCCATGTATG[A/T]GGTTTACACGAAGGC | 2074 |
rs535940916 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506660 | CAGATATAAAATAAG[A/G]TGAACACTTATATTT | 2074 |
rs535947851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485335 | AATCCAAAGCTAGTA[A/C]TATTGACACTAGGCT | 2074 |
rs535968387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489850 | CTTCTTTATCTCTTC[A/G]TTTACTACATTTTCT | 2074 |
rs536043364 | snp | A/G/T | 0.000296533 | 0.012173 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516837 | TGCTGCACAGTAAAC[A/G/T]TAGATGGAACTTCAT | 2074 |
rs536068550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523114 | AGGTCTCTTCACCTT[A/G]AGAAATAAGAAAAAA | 2074 |
rs536077729 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525606 | TTAATAGGAAGGAAT[C/G]CATATTCTAAAATCT | 2074 |
rs536089091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475908 | TATGTACCTGACACC[C/T]GCCCACCTACCAGGT | 2074 |
rs536096948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483083 | TTGTTGAAGCTGAAT[A/G]CTATAGATTAGAGTT | 2074 |
rs536098303 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479287 | AGAAAGTCAGCTGTA[A/T]AATGAATGATAATAA | 2074 |
rs536171316 | in-del | -/AAA | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519389 | TGACATGTAGAAAAT[-/AAA]AACATAAAAGAGGTC | 2074 |
rs536201473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517440 | CACCAAGTGATAACA[C/T]GTACCCTCAGGAGGC | 2074 |
rs536241638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460869 | ACTCCAGCCCGGGCG[A/T]AAGGGCGAGACTCCA | 2074 |
rs536274977 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466678 | CTGTCATGACTGTGT[G/T]TTTTCTAGAATTTTA | 2074 |
rs536356846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467208 | CATGTACAAGCCTTC[A/G]TATGGACATATTTTT | 2074 |
rs536370677 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492544 | TATCTATGCTACCCA[C/T]AGGAGCACAGATAAA | 2074 |
rs536467494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532125 | GAAAAATTGCCCAAG[A/G]ACTGAACACTAAGTT | 2074 |
rs536525906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480869 | TCTACAAACTAACAG[G/T]CCTATAGTCTTTAAA | 2074 |
rs536527385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488293 | AATCACACTGTCAGG[C/T]GGCGGGGAGAGGAGC | 2074 |
rs536552841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479907 | AGATTTCTCTACCAA[C/T]GCTCACATCCCAGTG | 2074 |
rs536564955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487544 | TGCCAGTGAAGAAAG[C/T]AGTCTGCCCAGAGAA | 2074 |
rs536597367 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533669 | TTAGCCAGGCCTGGT[-/G]ATGTGCACCTATAGT | 2074 |
rs536619242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514612 | TGTAAGGAAAAAGCT[G/T]TGTATCATACAGTTA | 2074 |
rs536693894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469918 | ATGTTCAGGTAGTAC[A/G]CATCGATTTAAGAAT | 2074 |
rs536724304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461318 | CCTTAGTTGTTTGGA[C/G]TCCTTGCAAGTATGG | 2074 |
rs536747584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500983 | TTTCAACATTAGAAA[C/T]AGCTTGCTAAACAAG | 2074 |
rs536757172 | snp | C/T | 3.29734e-05 | 0.00406025 | missense | ERCC6 | GRCh38.p7 | 10:49470424 | TTTGACTTGTGCTTA[C/T]AAAAATTATTTTCCA | 2074 |
rs536776226 | in-del | -/G | 0.0103295 | 0.0711199 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521812 | AAAGCAGGATCCAAA[-/G]GGCGACTGCCCAGTT | 2074 |
rs536785677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508253 | AAGTTTGGCACAAGG[C/T]CATTAAATATTTTAT | 2074 |
rs536804300 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492292 | TTTCCTGGGCCCCGA[A/G]AACGAACTCAAGAGC | 2074 |
rs536885571 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457472 | CATGTCCTCTCATGC[A/C]GTCCGGCAAGGCCCC | 2074 |
rs536907595 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534780 | TGTGAATAAGATTTC[C/T]TTGAGCACTGTAACT | 2074 |
rs536907872 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536257 | AGAGCTTGCCTCTGG[C/G]AGGGAGACAGCTACA | 2074 |
rs536942592 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469077 | ACAATAGAATGTTAA[A/T]CACCATTTGGCAACC | 2074 |
rs536942774 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491191 | TCCAATGTGTCGTCA[A/C]CACAAATAAGCCAAT | 2074 |
rs536956921 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471902 | TCTAAAATCCCCTAG[C/T]CATTATGGAAAGACA | 2074 |
rs536980180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497343 | CCAATCAAAAGCTGT[C/G]TAAAATATTTTTACA | 2074 |
rs537002410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484076 | TTGAGCCCAGGAGTT[C/T]GAGACCAGCCTACGC | 2074 |
rs537016339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517363 | AAATGTTTCTGAAAA[C/T]TCACATCACTTTTTG | 2074 |
rs537021318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510839 | CTTTCTGTTCTGTCT[C/G]ATTTAGAGCCTACCT | 2074 |
rs537074807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530290 | ACTTGCAATTTTTCA[A/G]CTTTGTGATGGGTTT | 2074 |
rs537140405 | in-del | -/TCT | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513855 | TATTCTCTCTCTCTC[-/TCT]TTTTTTTTTAACAAT | 2074 |
rs537145311 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478890 | TCCAAAAGCTACAAA[-/G]GAACTCTGCAAAGCT | 2074 |
rs537160754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463513 | AAGGAACAGAAGATA[A/C]TATAGTATACAACCT | 2074 |
rs537170095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477481 | GTCACTCCTGAAGCC[C/T]GCACCCAGAGCAAGC | 2074 |
rs537192302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518305 | ACAATGCTTGTCCGA[A/G]TCTGCTGCAGCAAAC | 2074 |
rs537245645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535643 | ATTCAACCAAAAATA[C/T]TAAGTAACCATTTTT | 2074 |
rs537255197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518989 | TATCAACAGGCATCA[A/G]GTCTACAGATTCAGG | 2074 |
rs537277895 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540259 | AGCCAAGCTGTCCGC[A/G]AACTCCTGACCTCAG | 2074 |
rs537332660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483239 | AAATTTCTTGTGCAG[C/T]TGGCACAAGGAAAGA | 2074 |
rs537371877 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537111 | AGCACTTTGGGAGGC[C/T]GAGGCGGGAGGATCA | 2074 |
rs537372458 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537213 | GCTGGGCATGGAGGC[A/G/T]CGCGCCTGTAATCCC | 2074 |
rs537470915 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526410 | GGAAGTGTTCCAGTC[G/T]TTCGCCCATTTTTGT | 2074 |
rs537477641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518813 | GTATTATCTTCGCAG[C/G]AGATTATGTCTCACA | 2074 |
rs537530480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481370 | GTATAACAGGAGATT[C/G]AGAGAAAGAAGAGAC | 2074 |
rs537549013 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473403 | CTTTGGTGGGTAAGG[C/G]TGTGGATACGCTTAG | 2074 |
rs537613914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508501 | ATTCTAGTGCCTTCC[A/G]CTTCATAAAGAAAGA | 2074 |
rs537686616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471896 | CCACTGTCTAAAATC[C/T]CCTAGTCATTATGGA | 2074 |
rs537700009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467356 | GTGTATGAGACCCAA[C/T]TGCTTCACATCTTTA | 2074 |
rs537748549 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488106 | TGTAAAATATGTAAC[C/G]TCTCCTAGTTTTTGC | 2074 |
rs537799148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480158 | CAGTCTATATTTGGG[A/C]TGCTGACATGCTCCC | 2074 |
rs537806900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487447 | ATACAGCAATAAACG[A/C]CTTGGGGTGCACAAC | 2074 |
rs537818597 | in-del | -/T | 0.0158469 | 0.0875917 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484678 | TCAGGAGTTAGAGTC[-/T]ACAGTGAGCTATAAT | 2074 |
rs537846611 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540164 | CTGCCTCAGCCTGCC[A/G]GGTAGCTGGGATTAC | 2074 |
rs537849051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533537 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAAG | 2074 |
rs537855158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509935 | TTCACTGGCTGTGTT[C/T]CTAGCTCCTCACACA | 2074 |
rs537883280 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539558 | GGAGTGAGTGCCTAC[A/G]GAGCCTGCTTACATG | 2074 |
rs537883794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462424 | ACAAGAAAACATGGC[A/G]AATTATCATATGATC | 2074 |
rs537921149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473764 | TATTTCCGTATGGTT[A/T]ATTCTTACTTTTGTA | 2074 |
rs537959632 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480695 | ACCACCTTAAAGTAA[C/T]CAGAGTTAACATCAC | 2074 |
rs538087994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474416 | AATTAACTTTCACTC[A/G]TCTTGTTTCCCTGAT | 2074 |
rs538089379 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500020 | TCTAGAAATGCTATC[A/G]TGCACACTCATTATA | 2074 |
rs538130190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475872 | ATATAATTCTGGTCA[C/T]AATATCTGGGAAAAT | 2074 |
rs538182178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508888 | TGCCTTCCTCATCCC[A/G]GACGCTGCCAAGAGA | 2074 |
rs538211580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502812 | CTGCACAGGACAGTC[C/T]CCACAGCAACAAATT | 2074 |
rs538318983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537127 | GAGGCGGGAGGATCA[C/T]GAGGTCAGAAGTTCG | 2074 |
rs538368530 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485485 | AATATGAATGAAACT[A/G]TTAAGAGGGGATCTA | 2074 |
rs538428236 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522384 | ATGTGGATATCTGCA[A/G]TTTAACAGCCTTAAT | 2074 |
rs538532600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472049 | ACATTCAACCTTGTC[A/C]TTTTTTAAAATTTTT | 2074 |
rs538532621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479087 | TGGAGCACGGCCACA[A/T]GAGATGAGTACTAAA | 2074 |
rs538602278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505725 | CCAATTTTAATGAAC[A/G]GCACGTGGCTATAAT | 2074 |
rs538627283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536362 | GGAGGGAGACAGAGG[A/G]GATAACCCAGAAAGG | 2074 |
rs538634442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513257 | CCCGTGGTGTCTAAC[C/T]CCTATGCTATATACT | 2074 |
rs538643019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504841 | TCACATCTTTAGAGT[C/T]TGGCTTTCTATAATG | 2074 |
rs538696439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472633 | GGAAGATGAACAGCC[A/G]GTTGAAAAGACATCT | 2074 |
rs538728187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460229 | CAAGTGAATGTGCAT[C/T]GTAAATCAGAGCGTG | 2074 |
rs538739845 | in-del | -/CTCT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49532011 | GCTCAAGTCTTCTCC[-/CTCT]CTAAGACACAAATAA | 2074 |
rs538758429 | snp | A/G | 0.000399281 | 0.0141238 | missense | ERCC6 | GRCh38.p7 | 10:49472937 | CTTGGGTTCCAGTCT[A/G]GGTCATAGATGACAA | 2074 |
rs538764050 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465834 | ATTAAACCTCTTTCT[G/T]TTGTAAATTGCCCAG | 2074 |
rs538765788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498078 | AGGTGGTGTATCCAT[C/T]ATGAAGGGGAACACA | 2074 |
rs538814325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500072 | TTCTTCAAAGCTCCA[A/G]CTCTCCCCATGAATA | 2074 |
rs538827316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531492 | ACAGGATAAACAATG[C/T]GTATTACTGGCTGAG | 2074 |
rs538827405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525119 | ATCAGCTGAGTAGTC[A/G]TCCATGAGGAAGCAA | 2074 |
rs538850567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507651 | CGTTCTTGACAGGGG[A/G]CAATTCTGTCCCTTC | 2074 |
rs538852594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499463 | ATGAGCTGGAGAGTA[G/T]GAAGAACTTTCGGCA | 2074 |
rs538863590 | snp | A/C | 1.65419e-05 | 0.00287588 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530880 | TTTTGCACTCTGATA[A/C]CATTTTTATAGCATA | 2074 |
rs538924327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532305 | CTTCTGGACATTATG[A/C]ATGCAACTGGCTTTC | 2074 |
rs538943785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493742 | ACTGATGGGGGCTCA[C/T]AAGGCTGGCATGGCC | 2074 |
rs538959294 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513070 | GTGGTAACTTTTAGC[C/T]AGTGGGCATGTAACA | 2074 |
rs538961162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486643 | CAAAATCTGAACATT[C/T]TGACAGATATGATAG | 2074 |
rs538974759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500920 | CAAAACATTAACACA[C/T]TTCTAATTAAACTGA | 2074 |
rs538997959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493055 | ATGGATCAGAGAAAA[A/G]CCAAATATGTAAAAT | 2074 |
rs539093662 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466542 | TAAGTTGTGACATTA[G/T]GTACATACCATGAAA | 2074 |
rs539126751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469896 | CATGTAAAGTAACTG[C/T]CTACTAATGTTCAGG | 2074 |
rs539165843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513786 | ATATGGGGACTACAA[C/T]TCAAGATGAGATTTG | 2074 |
rs539249237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510712 | TGGCAGACCGTTAAG[C/T]GCTGAATGAATGAAT | 2074 |
rs539281524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538918 | CCTGAGCTGGGCCCC[C/G]ACACCCCCTGCCCGA | 2074 |
rs539285189 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463471 | ATACTGCAGTGGCTG[G/T]CAGGATATATGAAGT | 2074 |
rs539334543 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523398 | GTGCTTGCTTTATAC[-/A]ATGACAATGTCATGG | 2074 |
rs539341530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496578 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACCTGA | 2074 |
rs539357939 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479548 | CATTCAGACTGATGA[A/G]TATCACCTTGAAGAT | 2074 |
rs539373295 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529546 | TTGGGAGGACCCACC[-/T]GCCTTGGGCAACTGC | 2074 |
rs539394408 | snp | C/T | 0.000732649 | 0.0191256 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516157 | ATTCCTCATGTTTAG[C/T]ATTTGGGTTTTTACC | 2074 |
rs539465367 | in-del | -/ACAT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537505 | TATATATATATATAC[-/ACAT]ACACACACACACACA | 2074 |
rs539475170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529233 | ACTTCAAATACGAGT[C/G]TGGGACAAGGGGAAA | 2074 |
rs539499463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523754 | AGCTCACACTCAGCC[C/T]TCTGTATGCCTCTTG | 2074 |
rs539506755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462698 | TCACAGAAAGAAAAA[A/T]TTTTTAAATATAAAT | 2074 |
rs539588684 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455139 | TTCTCCATATTTTTA[C/T]GTAAGTTAAAAGACT | 2074 |
rs539626308 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518243 | AGGAATGGGACATTG[A/G/T]GTTGGAGTTGGCCCC | 2074 |
rs539634432 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456461 | AAAACTCAAAAATTT[C/T]ATTAGTAAAGGAAGA | 2074 |
rs539674269 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455849 | ACGAGACTGGTTAAA[A/G]CAAAACAAAACAACC | 2074 |
rs539718592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490066 | GAAATCTTGAACTTT[C/T]ATTAAATGCGATTTC | 2074 |
rs539737866 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507495 | CTTCTAAAGGCAATC[A/T]CTTCTTCTCCACTGG | 2074 |
rs539747411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495925 | CCTCTCACTTCAAAG[A/C]CTCTAATGACTGCCC | 2074 |
rs539868211 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477078 | TCCTCTACGCATGCC[C/T]GCCCAGCATCTTCCA | 2074 |
rs539934960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465486 | GTTGGGAAGGCATGA[C/T]TGGTTTTAAAATGTG | 2074 |
rs539943619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485170 | TCACCACAGACCATG[C/T]TCACAGCAGCTCCCC | 2074 |
rs539963591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483138 | GGCCCCTACAAGAGA[C/T]ATTAAATAACATGAA | 2074 |
rs540003523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511697 | TCCAAAGTGCTAGGA[C/T]TGCAGGCGTGAGCCA | 2074 |
rs540041651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517529 | TCCCACATGCTTAGC[A/G]TTCCAATAATGGAAC | 2074 |
rs540086233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477242 | TGATTCCCTGGTTTT[C/T]ACTCCCTAACATGTC | 2074 |
rs540103255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460936 | TCTCAGAATGAGAAC[C/T]ACTCAGTATCTTGTT | 2074 |
rs540134425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464204 | GGAACTTGTTGGGAA[C/T]TGGAGCAAAGGTGAC | 2074 |
rs540141675 | snp | A/G | 8.31055e-05 | 0.00644561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460359 | CTGGAAAGCAAAAAG[A/G]TTATCTATATTACCT | 2074 |
rs540173425 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509367 | GAGAAAGCAAGTTAC[A/G]TATGTGGCCCAATGC | 2074 |
rs540196710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478738 | ACTGATAATTTTGTG[C/T]CTTATTTCTCTTATA | 2074 |
rs540277826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492785 | TTGAAGCCACTAATG[C/T]GCAAAGTCTCTCCTT | 2074 |
rs540286695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513057 | TGGTGGAATCTTTGT[A/G]GTAACTTTTAGCTAG | 2074 |
rs540326895 | in-del | -/AATAAAAC | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530993 | CCCTTATTGGCCACA[-/AATAAAAC]TTGTAGGATCATTAG | 2074 |
rs540328862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487598 | ACCTGGTCAGACCTG[C/T]GACCTTTAGAAGCCA | 2074 |
rs540344268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479352 | TAAAAAATTAACTTG[C/T]TAAAAAATGTTCTTA | 2074 |
rs540388391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481039 | TTGTTGCTTACACTG[G/T]CTATGTAAGAGGCGA | 2074 |
rs540406007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507403 | TATGGCCAAGTCTAA[A/G]GAAATAGCTATCATC | 2074 |
rs540433214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473302 | ATGCCCACAATCCCC[A/G]CCCCCAAATATCCAG | 2074 |
rs540442545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513391 | ATTATGACTGACAGT[A/G]ATACTGGGTACTGGG | 2074 |
rs540565822 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463494 | TATGAAGTTTTTTTA[A/C]AAAAAGGAACAGAAG | 2074 |
rs540572731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507799 | CTAAACATCCTACAC[C/T]ACACAGGACAGCCCC | 2074 |
rs540623710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500360 | ATGTTTAATTTCTCC[C/T]GCCCTACAGCTCCAT | 2074 |
rs540660409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538615 | TCGGACGTACATCTA[A/G]CCCGACTCTCTTTAA | 2074 |
rs540681571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503580 | CACACAGCTGGTAGA[C/T]GATATACATAGCTGG | 2074 |
rs540696121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526634 | CAATTAAGCCTTAGG[C/T]CTTTACACTGAGTAT | 2074 |
rs540704637 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520431 | AATGAGTTTAAGTCA[A/C]ATGATAAACACTAAC | 2074 |
rs540711933 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49541052 | TCTCATAGTTCTGGA[A/G]GCTGGGAAGTCCAAG | 2074 |
rs540714194 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527628 | TGCAGTGAGCTGAGA[C/T]GGTGCCATTGCACTC | 2074 |
rs540714920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490649 | TGAGCCACCACGCCC[A/G]GACAATTTTCAAAAT | 2074 |
rs540862049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523838 | AGACCTAGAAGTACA[C/T]GCATTTGGGGCCAGC | 2074 |
rs540904791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467665 | CAACCTCCCAGGCTC[A/G]AGCAATCCTCCCAGC | 2074 |
rs540919458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517832 | TACAGGTATGAGCCA[C/T]TGTGCCCGGCCAGGC | 2074 |
rs540945382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473973 | TCCCATTTTGTGAGT[C/T]GATGGCTGTCATAAA | 2074 |
rs540977780 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529022 | CTGTCCTTTTAGTAT[G/T]CTACCTAATCAAAAA | 2074 |
rs540982918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476906 | CCCTCTGCCACCTAC[C/T]TGGACCCCTTTCAAC | 2074 |
rs541005747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512480 | AATATTGATACTGTA[C/G]TTATATTTTTATAGA | 2074 |
rs541021349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495443 | AGCAAAATGCACATA[C/T]ATTACTCCACTGTAT | 2074 |
rs541040398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511889 | GGTAAGGGGAGGCCT[A/G]AACTTTAGAAAATAT | 2074 |
rs541094201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535808 | GAATTTGGATACCAA[C/T]GGGTCACCATTTACC | 2074 |
rs541132937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534898 | AGAATTCAGCATCAT[C/G]TACACCCGAGTGGCT | 2074 |
rs541165428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505268 | CACATCTATCAGGCA[A/G]CATCCGGTCATCTCC | 2074 |
rs541181830 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500035 | ATGCACACTCATTAT[A/G]AAGGAAATTAGGGAG | 2074 |
rs541240285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491638 | CATAATGAGTCCATG[G/T]ATGTGGTTTACACGA | 2074 |
rs541250653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523291 | CACCATGGGGAGGCC[G/T]GCAATACAGATTATT | 2074 |
rs541266472 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497671 | GTCACATCGTCAACT[C/G]AACCACCCTTTCCTA | 2074 |
rs541267594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536461 | CTCGGACTCTGGCAG[A/G]AGGAGGATTCCTGAT | 2074 |
rs541277252 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49530177 | GCCAAAGAAATGGTG[A/G]TGCAGGAAAACTAAG | 2074 |
rs541291332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531153 | TATGCTAGAACAATG[C/T]GCAATAAGTTGTCCT | 2074 |
rs541392893 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504510 | ACTTGATCCTTGAGG[A/G]TATCTGCCAAATCAC | 2074 |
rs541408772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514872 | AGATACTTGGTGTTT[C/T]ACTTTTCTTATCTTC | 2074 |
rs541447455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514132 | ATCCAAATGTTGTCT[C/T]AAAAAAACATCAGGA | 2074 |
rs541448161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507925 | GAAACTGAACAGATA[A/T]ATATACACTTTCCTG | 2074 |
rs541454132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471287 | AGGAAATATATAATA[C/T]ATCAGTTAATCTCCC | 2074 |
rs541540959 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457924 | AGGCAGGCGCAAGAC[A/G]AAGGCAACTGGAGAG | 2074 |
rs541542967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464867 | ACTCCTAGATGCCCA[A/G]GCAGAAGTTTGCTGC | 2074 |
rs541576689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498728 | TCATTCTTAGTAGGA[C/T]TGTCACCACCCAAGA | 2074 |
rs541647093 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455174 | ACCAAAACTAAAAAT[A/C]TATAAAACACCTAGG | 2074 |
rs541664126 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539215 | TCTACTTGCGTGCGA[A/G]CAGGGCGAGAAAGCT | 2074 |
rs541760333 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514369 | ACAAATCAATGTACA[-/C]CAACTGCCCATACCA | 2074 |
rs541782699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484446 | GTCTGAATTCCAAAA[A/C]TAAATAAAAACAGCC | 2074 |
rs541880462 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479766 | CAGGGCTAGGCTGGG[C/G]AACGGCCGGGCTGTG | 2074 |
rs541884763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467019 | CTCCTGACCTCAGGT[A/G]ATTCACCCACCTCGG | 2074 |
rs541900352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468348 | TGCCTGGACTCCCAT[C/G]TGGGTTCTCCCTCTT | 2074 |
rs541909446 | snp | A/T | 4.32217e-05 | 0.00464855 | missense | ERCC6 | GRCh38.p7 | 10:49461556 | ACACTGTGCACGCCA[A/T]CTAGCAAGAAAAGAA | 2074 |
rs541966306 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507766 | ACTGGCATCTTGCAG[A/G]TGAGTCCAGGTATGC | 2074 |
rs541973200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482302 | CTTTATAAGATGCAC[C/T]ACCCCAGTTTGCAGG | 2074 |
rs542053472 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457501 | CCCCTGCCCAGAACC[C/T]TCCTCTCTGAGTCAC | 2074 |
rs542088381 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480930 | GTCCCAGATTAAAGG[A/G]GACTAGAGACACGGA | 2074 |
rs542122843 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462864 | GCTCGTGACAATTCA[A/C]ATTGATCTAAACCTT | 2074 |
rs542125123 | snp | A/T | 1.66496e-05 | 0.00288522 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516125 | AAACTGAAGGACAAG[A/T]GACGCACCGACACCA | 2074 |
rs542157937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481873 | AAGATCAGGTCCAGG[C/T]CCTCATGGCCCTCAC | 2074 |
rs542171180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494486 | TAGGTATACGTAGAA[A/G]AACTGGTTGTGGCCA | 2074 |
rs542198960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522070 | GCAAAGGGTGCCTAC[C/T]CTGGGAACTACTCCT | 2074 |
rs542218880 | snp | C/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457371 | ATCCAAAAAAAACTA[C/G]AAAATCCTGACAGGA | 2074 |
rs542257130 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513856 | TTCTCTCTCTCTCTC[-/T]TTTTTTTTTTAACAA | 2074 |
rs542419620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510353 | CACCGTGCCATACCA[C/T]GTATGCAGCCTCCTC | 2074 |
rs542479449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465950 | AGGTAAGGAAGGGGT[A/G]GGGACAGGGTGGGGG | 2074 |
rs542547781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503148 | TCTTTTTGCTTGGGG[C/T]TCATCAACTTAACTA | 2074 |
rs542571130 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477222 | GAACCTACCAGGATC[-/A]GGCATGATTCCCTGG | 2074 |
rs542593846 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510897 | CATATGACTTTAAAG[A/C]ACTGCTCCTAGCTCT | 2074 |
rs542603571 | snp | C/T | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506290 | GCTCCTCTTCTGGCA[C/T]ACCCTAAGGGAAAAT | 2074 |
rs542648206 | in-del | -/CAAAT | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531353 | GTGGTGCAAAGAAAA[-/CAAAT]CAATTTAAAATAAAT | 2074 |
rs542664606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525140 | GAGGAAGCAAGCTCC[A/G]AAGTTCTCACGTCAT | 2074 |
rs542685261 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478571 | AAAAAAAAAAAAGAA[A/T]AACCAACAGCTGTAT | 2074 |
rs542701041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485903 | GACATTCCACTGGGT[A/G]AGGCAAAAACCTAGC | 2074 |
rs542704560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518708 | CTCCCTCCTCAGAAC[A/G]GTGGATGTGCACAAC | 2074 |
rs542766493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486706 | AAAATCAGACCAACA[A/G]AACAAACCAATACTG | 2074 |
rs542777710 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465831 | TCAATTAAACCTCTT[C/T]CTTTTGTAAATTGCC | 2074 |
rs542831046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513001 | TTATACACCCTCCTT[C/T]ACGGTTCTCACAGAC | 2074 |
rs542867774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519253 | AACATGTATGTAGAG[A/G]GCCCAGCCGACTTCA | 2074 |
rs542872695 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520442 | GTCAAATGATAAACA[C/T]TAACCCTAGTCCTGC | 2074 |
rs542924001 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520907 | TGATGCACCTGGAGT[C/T]TAGGGGCAAATGCGT | 2074 |
rs542979551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499624 | AAACACAAGGAGCTC[A/G]GACTTATCTGGGTTC | 2074 |
rs542983169 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503053 | CCAGCTCCTCCAGTC[A/C/G]GGGAACAAAATCTCC | 2074 |
rs542985053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494767 | ACTTTTCTCTCCTGG[C/T]CTTTCTGGCTACATG | 2074 |
rs542992520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513321 | AGTTTTGTTTTGAGA[A/T]TACATATACACACAT | 2074 |
rs543018225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507156 | AGAGCCCAATGCTAG[C/T]ATGTAGGTAGCTACT | 2074 |
rs543057449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510288 | TTAGAAGAATTTTCA[A/G]CATTCCAAGGATGTT | 2074 |
rs543078215 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498110 | CAACCAGTACAGATG[C/T]TTATTAACCATAAGC | 2074 |
rs543083780 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517439 | GCACCAAGTGATAAC[-/AT]GTACCCTCAGGAGGC | 2074 |
rs543107848 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495967 | GACAGAGATTAAACA[A/C]CTGGACGTGGCCTAC | 2074 |
rs543145995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495301 | CTAAAAACTGGGATT[C/G]ACTGAGGGCATCACA | 2074 |
rs543161974 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455942 | GTGAATTGATGCAAG[A/C]AATTCTGCTACATCC | 2074 |
rs543167522 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463815 | TCCATGTAAGATGTG[A/C]CTTGCTCCTCCTTGC | 2074 |
rs543168342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490180 | TTTTTGCATGGCTGC[C/T]GGGTGTACATTTGAC | 2074 |
rs543202976 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526568 | AGAAGTTCTTGGTTT[C/T]ATATATAGTCCATTT | 2074 |
rs543247582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529347 | TTTCCCTCTGAATAG[G/T]CTACCTCTAACCATC | 2074 |
rs543270922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523248 | AGGAGACTTGAAATG[C/T]GCGGCAGTAGCACAG | 2074 |
rs543286428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534770 | TTTGTTTAACTGTGA[A/G]TAAGATTTCTTTGAG | 2074 |
rs543287265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473258 | AAAATACATGCTGTA[A/G]AAAACGCATTCTTTG | 2074 |
rs543313748 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473191 | AATCTCATTTCACAG[C/T]TTTTACTTTTAATAT | 2074 |
rs543322428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480247 | CTGAGCCCCATAAGC[C/T]CTGACACTGGGCATC | 2074 |
rs543455408 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455435 | TGGAACAGAAAACAC[C/G]CAAGTATAAGACACT | 2074 |
rs543477404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534263 | AGGAGAAGGATCCCC[C/T]CTCACATAGTGCTGC | 2074 |
rs543492867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523412 | CAATGACAATGTCAT[A/G]GAGCTAAAAGCCAAA | 2074 |
rs543497841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489520 | GATTCGAACCCTGGT[C/T]TTGTAAGCACAAAAC | 2074 |
rs543526727 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489823 | GTTATGGGATAGGTA[C/T]CACAAGACTGCCTTC | 2074 |
rs543550329 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540363 | CTTTTTTTTTTTTTT[A/T]AAGGAGAAAGAATTC | 2074 |
rs543656324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533022 | TCGTTATATAGGATT[C/T]ATTGTAGTTCTTAAA | 2074 |
rs543663475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504446 | AGTACTATTAATTGT[A/G]AAATATCTTTGCTAG | 2074 |
rs543664506 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536223 | AATGGAGGCCACAAG[A/C]GAGTGGCCTGTCCTT | 2074 |
rs543677055 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536425 | GCAAGCAGAAATGAA[C/G]AGGAGGCACAACACA | 2074 |
rs543714597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536045 | CGCTTGAACCCAGGA[A/G]GCAGAGGTTGCAGTG | 2074 |
rs543772022 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504540 | CTTACTACAAATACA[C/T]AGAAGTATCCTGTCT | 2074 |
rs543786723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511114 | TCTGAGCTCCATTTT[A/T]TGGGTTCATCACCAG | 2074 |
rs543825951 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519894 | CAGCTCCTCCCACTC[A/T]GCACCTGCTGCCTCA | 2074 |
rs543840830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476805 | CTCCATGCGATCGTG[A/C]TCTGTGACCCTTCAC | 2074 |
rs543847100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513630 | CTTCTTCACAAGGCG[A/G]CAGGAGGAAGTGAGT | 2074 |
rs543900788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463799 | TCTTTGCCTGCTGCC[A/G]TCCATGTAAGATGTG | 2074 |
rs543967433 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505012 | GGCTGACAGCTGAAT[A/C]TATAAAGGAGACCAA | 2074 |
rs543974321 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49482347 | TGTTCCAAACTGATT[C/T]GTCCTTGTTTCATAA | 2074 |
rs543999610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466184 | TATTTTTGACTCAAG[C/T]AGTGTTTTGACCAAA | 2074 |
rs544004724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497097 | CTACAAGAAGCCAGA[A/G]GCTACAAGAGACTCC | 2074 |
rs544021571 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508422 | CTCCTAAAATATACA[A/G]GCATCTTGTCGCCAC | 2074 |
rs544120727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491519 | GGTAAAACAACCTCA[A/G]AAGGTAAAGCCACTG | 2074 |
rs544155912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490934 | CATTAGACGCTGAGT[C/T]AGAGGACGAATCACC | 2074 |
rs544161593 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497574 | TTAGTAGAAAAAATT[A/G]GAGATTTTCACGCTG | 2074 |
rs544182243 | in-del | -/T | 0.39527 | 0.203462 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488643 | AATGTGGCCTCTTTC[-/T]TTTTTTTTTTTTTTT | 2074 |
rs544184505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472848 | AAGGACAGTCAAAAG[C/T]GCTAACCATGAAACT | 2074 |
rs544281889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466791 | TTTATTGTTGATTAG[C/T]ATATATATTTTTTGA | 2074 |
rs544283746 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480521 | TCCAAAGATCTCACC[C/T]GCTAGGAAGGGGAGA | 2074 |
rs544296985 | in-del | -/AAAGTA | 0.00164733 | 0.0286523 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474286 | CAGATGACCCCATGT[-/AAAGTA]AGATTCCCTAGGCAA | 2074 |
rs544403309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507828 | CCCAAACCCCTCGGT[A/T]AAAAGTTATCAAGTC | 2074 |
rs544412107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488655 | TTCTTTTTTTTTTTT[C/T]TTTAAAGTTTTTTAC | 2074 |
rs544444106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461043 | TAATGTGTGCTGTAA[A/G]CTGGCTAATTATCTC | 2074 |
rs544456722 | snp | C/G | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540979 | TTCCCAGCTGCCTTA[C/G]CTCAGGCTGCCATAA | 2074 |
rs544466390 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49539101 | GACTCCGACTTCTGC[G/T]GGTGCGGGGAGGCCC | 2074 |
rs544471829 | snp | A/T | 0.000247188 | 0.0111145 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482834 | TTGCATCGGTGAGCC[A/T]GACAGAATGATCCGA | 2074 |
rs544489749 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468911 | GAGCCAGCTTGAAGG[A/C]GCTCCCACCCATGAG | 2074 |
rs544493713 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457916 | GAATGCAAAGGCAGG[C/T]GCAAGACGAAGGCAA | 2074 |
rs544506076 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460707 | AGGCAGATCACTTGA[A/G]GTCAGGAGGTCGAGA | 2074 |
rs544526702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468267 | CTCCGCTATCGTCTC[C/T]TGCATGTGAATGCCA | 2074 |
rs544548574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493325 | TGCTCAAAAGATCCC[C/G]CAAAACAACAAACAA | 2074 |
rs544616303 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527233 | TATTAACCCTACTAC[C/G]AAAGTCACAGTAGGA | 2074 |
rs544649668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490746 | ACAATTCTGGCATTA[C/T]TATTCTTTTAAATAT | 2074 |
rs544725788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481229 | ATGTTTGCAAAATGC[C/T]AACAATCAGTGAATC | 2074 |
rs544737344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483686 | CTGGCAAGTAGTAAA[C/T]GCTGACTAATACAGC | 2074 |
rs544756766 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463082 | TACCCAAAATTCTTG[C/G]GACCAGAAGTGCTTC | 2074 |
rs544762667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477688 | ACCCTCCTCCTTGCT[C/G]CCAGCCCTGACCACA | 2074 |
rs544775344 | snp | A/G | 0.000148293 | 0.00860957 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515695 | CACGGATTGATGCCC[A/G]ATACTTATCAATGTT | 2074 |
rs544819422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519539 | TTCAGGCTATGCATT[C/T]AGCAGCTTAGCCCAA | 2074 |
rs544844383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521973 | GGATGAGATATCCAG[A/T]AGTCACCCACTCTCA | 2074 |
rs544920485 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527558 | GTATGCGCCTGTAAT[C/T]CAGCTACTTGGGAGG | 2074 |
rs544920842 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471406 | AAACACCTTTTCACA[C/T]GCCATCATGTGACTC | 2074 |
rs544934244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509308 | TTTCTGAAATCCTCA[C/T]GACAACCCTGCAGCA | 2074 |
rs545019491 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512512 | ATTTTATCATTAAGT[G/T]GGCCTTAAGCTTATT | 2074 |
rs545085735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530438 | ATATTTTCAATTTAC[A/G]ATGGGTTTGTCGGGA | 2074 |
rs545145354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537291 | GGAGGCCGCAGTGAG[C/T]GAGATCGCACCACTG | 2074 |
rs545145840 | snp | C/T | 1.64866e-05 | 0.00287106 | missense | ERCC6 | GRCh38.p7 | 10:49470815 | TGCGTTTTGGAACAT[C/T]ATGGTCTGCTCCAAA | 2074 |
rs545195632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525230 | ATCACCATGTACCTA[A/C]AAAGGAAAAACATAA | 2074 |
rs545229135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462089 | ACCTTCATGAACAGA[C/T]CAGAAAACACTGAAA | 2074 |
rs545241410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485007 | CTTCAGATAGGCAAG[A/G]ACTTGGAAGATCAGT | 2074 |
rs545373847 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501767 | TCAAGACCAGCATGG[G/T]CAACATAGTAAGACC | 2074 |
rs545373937 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509214 | TAAATAAGGTGTCAC[A/G]TATAAAGCACCTTAG | 2074 |
rs545380524 | in-del | -/TTTTAC | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514869 | TTGAGATACTTGGTG[-/TTTTAC]TTTTCTTATCTTCCT | 2074 |
rs545411619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508637 | CCCAGTAGAATTATA[C/T]ACATATTAAAGACAG | 2074 |
rs545430255 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535767 | AAAAGGAGGAAGAGC[A/G]TCCAGTGAATGAGAA | 2074 |
rs545477530 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497328 | GGGATTAGGAAACAA[C/T]CAATCAAAAGCTGTC | 2074 |
rs545491384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459368 | AGGGTGAGACTGAGA[C/T]TCCACCTAATGAAAA | 2074 |
rs545535414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502314 | ATTATAATACACACA[C/T]TGGATATGCACCTTG | 2074 |
rs545540128 | in-del | -/TCT | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511415 | TAAGTGTGTTGTTCA[-/TCT]TCTTTTTTACTTTTT | 2074 |
rs545559453 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519770 | TGCCTCAAAGCTCTC[C/T]TAAATGAGAACATAG | 2074 |
rs545583479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531824 | ATCCCGTTCAGCCCT[C/T]GCCTTCTTTCTTGCT | 2074 |
rs545629394 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533717 | CTGAGGCAGGAGGAT[C/T]ACTTGAGCCTGGGAG | 2074 |
rs545750406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478862 | ACAAATCTCTGTTTA[C/T]GATCTTGTATTCTCC | 2074 |
rs545862230 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461709 | TAAAAAATAGTAAGA[C/T]AATTCAAGCAACATA | 2074 |
rs545928008 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535300 | TGCAAATCTGAGCTC[A/G]AGGGAAAGTCTGGGT | 2074 |
rs545931375 | snp | C/T | 0.000181379 | 0.00952138 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517042 | GTGGTTGTATCACTA[C/T]AGCACTTGCTTCTAT | 2074 |
rs545987811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494536 | CCTCTCCCTTTTTCC[C/T]GAAGAATCAGATCTC | 2074 |
rs546047426 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509368 | AGAAAGCAAGTTACG[C/T]ATGTGGCCCAATGCA | 2074 |
rs546069429 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476200 | CATTTCTCCAGCTTC[C/T]ATTTTTTAGCTGACC | 2074 |
rs546094499 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456733 | ACACTGTACAAAGCT[C/T]TTAAAGTTCTAAAAA | 2074 |
rs546104638 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513482 | ATACTATATTGTATG[A/T]GTCCATTTTCACTGC | 2074 |
rs546117443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482346 | CTGTTCCAAACTGAT[C/T]TGTCCTTGTTTCATA | 2074 |
rs546147831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464644 | GGCCCATGGTCCCCA[G/T]GCTGTGTGCAGCCTG | 2074 |
rs546180358 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475483 | TGAATAGATGTGAAT[G/T]ACTGAAGAACCTCCT | 2074 |
rs546206351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522644 | GATATATTTTAAACA[G/T]ATTTAATATTGACCC | 2074 |
rs546310729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465099 | CCCATGAAAGCAGCC[A/C]GGAGGGGGGCTATAC | 2074 |
rs546407915 | snp | A/G | 6.59326e-05 | 0.00574125 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482843 | TGAGCCAGACAGAAT[A/G]ATCCGATGAGGGGTG | 2074 |
rs546462742 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491949 | GTTTGACTAGACAAC[A/C]ATCTATACTGCTATT | 2074 |
rs546493661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497988 | AAATTAACTGAGTTT[C/G]AAAGTCAATTTATTT | 2074 |
rs546518461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496152 | TCCAGCTACCTTCTA[C/G]TCAACATTCAGATCT | 2074 |
rs546536810 | snp | C/T | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471743 | CTCCCTCGAGGAAGA[C/T]GTAATGTTCCAGGAA | 2074 |
rs546562185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486053 | ACAAAAAGGAGTGAA[C/G]AGAAAGAGGGATATT | 2074 |
rs546563841 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479079 | TTCTGTAATGGAGCA[C/T]GGCCACATGAGATGA | 2074 |
rs546581907 | snp | C/T | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539205 | GCAGCGCCTTTCTAC[C/T]TGCGTGCGAGCAGGG | 2074 |
rs546600583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485295 | TAAGTGGTGGAGTCA[A/G]AATTCGAACGGAGAA | 2074 |
rs546611524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512703 | GATATGTTGGGATGG[A/G]ACCCAAGACTAAATA | 2074 |
rs546672804 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505687 | AACATACCCAATGCA[C/T]ATTTTAGTCAACTTA | 2074 |
rs546814657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472529 | ATGACAAGCACTGAC[C/T]ATAAGAAACAAAGCT | 2074 |
rs546815793 | snp | A/G | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539298 | GAAAAATACCCTGCT[A/G]GCAAGGCAGTTATGA | 2074 |
rs546833790 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506388 | GAGTGTCTTCACAAC[C/G/T]GCAATACTATGTAAC | 2074 |
rs546843502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508073 | ATCAAAACTATGAAC[A/G]CAGAGCCAAACTTCT | 2074 |
rs546864621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537116 | TTTGGGAGGCCGAGG[C/T]GGGAGGATCACGAGG | 2074 |
rs546895303 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49505273 | CTATCAGGCAGCATC[C/T]GGTCATCTCCAATGC | 2074 |
rs546920285 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492454 | TATAAAAATGAATCA[C/G]ACACAGTCCCTACTC | 2074 |
rs546961992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481978 | AACCAGCATCCTCCA[G/T]AGTCCTGCTCAGACA | 2074 |
rs546976395 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526211 | TTTTCCAAAGTGTTA[C/T]GTTCCAAAGTCCCCA | 2074 |
rs546976421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490994 | AAACATAGACTCTAT[C/T]GTAATTTAACACACG | 2074 |
rs546998341 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467117 | GATATGCCATGGTTA[C/G]TTTAACTATTTACTT | 2074 |
rs547014227 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458134 | GGAGAGAAAAAGATG[C/T]CCTCTGCTTAAAGGA | 2074 |
rs547037784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519957 | CTGAAGGTGTTTCCC[A/C]TGTGATTCTGACACA | 2074 |
rs547048434 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529912 | TTCATAAAAATAATA[C/T]CCTAAGTAACAAATA | 2074 |
rs547051067 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489622 | AAACGAAACAAAACT[C/G]TTTAAATTACCTAAG | 2074 |
rs547072937 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487546 | CCAGTGAAGAAAGCA[A/G]TCTGCCCAGAGAAAA | 2074 |
rs547117890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525979 | TGTTGAATGTAGCTG[C/T]AGTTTGTTAACTCTC | 2074 |
rs547177921 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510570 | TGGGATCTCTACTAC[A/C]GTGCCCATCAAGTGT | 2074 |
rs547200496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513741 | CCGCCCCCATAATCC[A/G]ATCACTTCCCATCAG | 2074 |
rs547297968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461169 | ACAGGGGATGAAAGC[A/C]AGGAGGAAGGCAAAG | 2074 |
rs547312622 | in-del | -/TTCT | 0.00914312 | 0.0669923 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517621 | AAAATGAACACAGTC[-/TTCT]TTCTTTTTTTTTTTT | 2074 |
rs547335773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460647 | AACTGCTGGCTGGGC[C/G]CAGTGGCTCATGCCT | 2074 |
rs547408241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528281 | GAATAAAATTTTCCT[A/T]AATCTGTTTTGACAC | 2074 |
rs547452910 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496468 | GGGAATCATAAGTGA[A/T]TTTTGTTTTCTTACT | 2074 |
rs547470831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522253 | AAAGATCAGCAATGA[A/G]TAACAAAATATAGAG | 2074 |
rs547488502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503907 | CACACTAACCCAAGA[C/T]TGCATTTACTAGTGT | 2074 |
rs547503877 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475188 | ATTGTGATGTGCTGC[A/G]TATGTAAAATACATA | 2074 |
rs547539331 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454640 | ACAGGGCCCTTCACA[C/T]TGCCATTCTGGAAGT | 2074 |
rs547624966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530239 | AAAAGGAACTTTTCT[A/C]AAATACACAGATGGT | 2074 |
rs547693576 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456325 | GGGGAATGTCAAGGA[C/G]AGTGCATACCCTGCT | 2074 |
rs547810885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477202 | ACAAAATGAAAATCA[A/C]ACCTGAACCTACCAG | 2074 |
rs547860991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532130 | ATTGCCCAAGGACTG[A/T]ACACTAAGTTTGGGG | 2074 |
rs547895746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538264 | CAGTTCTGAGAGGGG[A/C]CAGGCAAGGGCCAAA | 2074 |
rs547985511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483928 | TAGGATCTCTAACAA[C/T]GTATAACAAGAATTC | 2074 |
rs547995826 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498948 | GAGTTTGGGGTTGTC[C/T]AGTTACCAAAAACAC | 2074 |
rs547996154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467607 | GTCTCGCTCTGCTGC[C/T]CAGGCTGGAGTGCAG | 2074 |
rs548020389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483107 | TAGAGTTGGGTTTGG[C/T]TACATTCTAACAACT | 2074 |
rs548033657 | snp | A/G | 0.000345898 | 0.0131465 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524627 | TTTTCGAAGCCTGAT[A/G]CTTCATTAAGCATGA | 2074 |
rs548060608 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471285 | TCAGGAAATATATAA[C/T]ACATCAGTTAATCTC | 2074 |
rs548144172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499931 | TATTACATAAAGTTC[A/G]TAGATTGGGAAGGGC | 2074 |
rs548249894 | snp | C/T | 0.000101642 | 0.00712814 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460487 | CAGTAGATTAAATGT[C/T]TGCTTTTGAGACTTA | 2074 |
rs548270039 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474711 | TTAATATGAGTCAGA[A/G]GTTGAGGATCCATTT | 2074 |
rs548354600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492901 | ACAGACATTGTCACA[A/G]CACCACCACAGACTG | 2074 |
rs548365178 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538847 | AGTGCGTCCTCGCTG[A/C]CAGGCTCAATCACCA | 2074 |
rs548405679 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486327 | CAGCACTTTAGACTA[C/T]ACAAAGAATATTCAT | 2074 |
rs548428601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520788 | CTCCCTGTCCTCAGC[C/T]TCTCTGCACATTGTG | 2074 |
rs548455303 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | ERCC6 | GRCh38.p7 | 10:49473485 | ATGTTACCTCATTGT[A/G]TCTCGTAATCAGTGG | 2074 |
rs548520334 | snp | A/T | 4.94694e-05 | 0.00497316 | missense | ERCC6 | GRCh38.p7 | 10:49470442 | AAATTATTTTCCATT[A/T]GTTTATTCTCCCAAA | 2074 |
rs548604140 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455503 | TGGCAAAACACAATG[A/C]AAAGCACCAAATGAC | 2074 |
rs548624754 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478646 | ATAAGTTCCATATAC[-/T]CCAAGGGGTGGTAGC | 2074 |
rs548627913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514646 | CATTCTTAATACAGA[C/G]TGACATTTCAACCTC | 2074 |
rs548639328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495004 | TTAGGTGCAGTCAAA[C/T]ATCCTGATACGTCCT | 2074 |
rs548642889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464604 | GGCCCAGAGGCCCAG[A/G]GGGAAAAAGTGGTTT | 2074 |
rs548654708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508756 | GTAGCCAAAATAGAC[C/G]TGACCATCTGATGAG | 2074 |
rs548687511 | snp | C/T | 1.65247e-05 | 0.00287438 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470870 | ATGGCATTTGGGTGT[C/T]TGAACATCTGATCCA | 2074 |
rs548687523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464149 | TTGATAGTGATATGA[A/G]CAGTAAGGTCCAAAC | 2074 |
rs548749912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494224 | TAACCTCTGGGAACG[C/T]CAGTTTTTCATTTTC | 2074 |
rs548763487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512028 | TAAATTTCAGATGCT[A/G]TAACAGTTGGCAGAT | 2074 |
rs548777282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501956 | CAGAGTGAGACCCCA[C/T]CTCTAATAAATAAAT | 2074 |
rs548802964 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465043 | AGATCCACTGACAGC[C/T]TGCACCATGCACCTG | 2074 |
rs548905296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491234 | GAAAAGTAATAAATA[C/T]AGGGCTTCTAAGTTA | 2074 |
rs548929040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504689 | AAAGTGGCCTTTATT[C/T]ACCTTTCCATAGTTA | 2074 |
rs548945088 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458340 | CTTTGTGGGTGGCAA[A/C]TGGTAAATATAAATG | 2074 |
rs548952991 | snp | C/T | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511487 | TGGAGTACAGTGGCA[C/T]GATCTCAGCTCACTG | 2074 |
rs548959489 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518618 | CCTAAAGGCTGCAAC[A/G]TTCCAAATCCACAAG | 2074 |
rs548966675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491888 | AACCACAAATGTTTT[A/G]CAAGGGTAGTGACAG | 2074 |
rs549071322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484520 | TGAGGGAGGAGAATC[A/G]CTTGAGGCCAGGAGT | 2074 |
rs549093531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485080 | TGGAGTGGTGCAGTC[A/G]TGGACAAAGAGGAAG | 2074 |
rs549104003 | snp | A/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523420 | ATGTCATGGAGCTAA[A/T]AGCCAAAGTCAGTCT | 2074 |
rs549191820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519533 | ATCCACTTCAGGCTA[C/T]GCATTTAGCAGCTTA | 2074 |
rs549214715 | snp | A/G | 0.000296868 | 0.0121797 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524826 | CATGAAACTTTCCGA[A/G]GGTACAAAAGAAATG | 2074 |
rs549225948 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490604 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 2074 |
rs549254408 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497520 | TGAACATCTATCTGG[C/T]ATTATCAAGATGCCC | 2074 |
rs549311881 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487645 | TGGACATCACCTAGT[A/G]TAGCTGGAGCTTTCC | 2074 |
rs549361892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506890 | GGTGCAACTGATGCT[C/G]TGAATTTCACAAAAT | 2074 |
rs549392292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460049 | GACTTTTATTTCAGA[A/G]GGTTGTGGTCTCTGG | 2074 |
rs549425113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472879 | ATATTTCTACTAATA[C/T]ATTCTTTTAAAAAAA | 2074 |
rs549443351 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537408 | ACTGAGAGTTAATTA[C/T]ACCAGGCAATGTACT | 2074 |
rs549445878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462313 | GTTGGGGCACAAACG[C/T]TGGGGCATTTTATCT | 2074 |
rs549597920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522157 | TTCTAATCATCCATC[A/G]TCAAACCACTGCTAA | 2074 |
rs549604424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481944 | TTGTGACTACCCTGT[A/G]GCCTGAGGAACCCCT | 2074 |
rs549626417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516582 | AAACATTTGAATTCA[A/G]AGCTAGTCAAGCCAA | 2074 |
rs549639180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488861 | TGATCTCAGCTCACT[A/G]CAAGTTCCGCCTCCC | 2074 |
rs549680370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466348 | CATGTATCCTAGGAT[C/T]GACAAGTAACTCAGT | 2074 |
rs549793404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533275 | GATGGCCATGGAATA[C/T]TCTTCAAAACAGCTG | 2074 |
rs549856731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527585 | GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCCG | 2074 |
rs549863058 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495794 | TGAATCCTTTCAGTC[A/G]CCATGTCTCTCCGTC | 2074 |
rs549880272 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540799 | AGTTATTTAGCAAGT[C/T]GTCCAAGCCCTTTTA | 2074 |
rs549891365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503330 | ATCTACAAATCTAAT[A/C]TTCGACGGCTTTCAA | 2074 |
rs549896217 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474475 | CTACTGGACTGAACA[C/T]GTCTACAGGGGTCAT | 2074 |
rs549931962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510521 | GTCCTGTCTTCCAAG[A/G]GCCCTCCCAATCCCG | 2074 |
rs549950510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499372 | AATAAAACACTAAAC[C/T]CTGGAGACTAAAGAA | 2074 |
rs550009151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510010 | CAAGAGAAGCTGGGA[A/G]CAAACATAAACCTAC | 2074 |
rs550025453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462446 | CATATGATCTATATG[C/T]AGAAAAGGCTTAGAA | 2074 |
rs550113815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468619 | TGCATATATATGCAC[A/G]TATGTATGTGTATAT | 2074 |
rs550132975 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477502 | CAGAGCAAGCCTCAC[A/G]GGCACCTCTGTTGAT | 2074 |
rs550149365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535064 | CTGAGATTTGAACAC[A/T]TGGGCCATGCATGGT | 2074 |
rs550189109 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455643 | AATATTTGTTGATCA[C/T]TGGAATAACTGCCTT | 2074 |
rs550196665 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536823 | CAAAAGAGTCACGGG[A/G]TTGAAGATGCTGAGA | 2074 |
rs550210693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529611 | AGTGAGAGAAGATGG[A/G]GTAGTGCAGGTAACA | 2074 |
rs550229835 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534472 | TTCTGTATACTGATA[A/C/T]AAAAGCCATGTTAAG | 2074 |
rs550362821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490351 | TTTTCCAAATGAAAA[A/C]TTTTCCTTTTTTTTT | 2074 |
rs550385874 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537534 | ACACACACACACACA[A/C]AAATATAATTGTGGT | 2074 |
rs550390439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529162 | CTTCACTGGGGAGGC[C/G]CAATGAACTGGGCTT | 2074 |
rs550399471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489804 | ATGTCACCACCTACT[A/G]TGAGTTATGGGATAG | 2074 |
rs550400581 | in-del | -/TA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502364 | AAACACGATGAAGTG[-/TA]TAGTACAGATACAAG | 2074 |
rs550407599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496220 | TGTAAACAAGTTAAC[A/G]ACTCTTCCTTAGTGC | 2074 |
rs550441482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483745 | AGATGACAAAGTTAT[A/G]ATACATATATTTATA | 2074 |
rs550462450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523629 | AGTTCTCTAAAATTA[C/G]TTTCCTGCTTCAAAA | 2074 |
rs550511485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465571 | CCAGCCAAATCTCAT[C/T]TTGAATTGTAACTCC | 2074 |
rs550516110 | snp | A/G | 1.65263e-05 | 0.00287452 | missense | ERCC6 | GRCh38.p7 | 10:49472967 | ACTCTGTTTGCCCCC[A/G]TCAGGTTGACACCTA | 2074 |
rs550638809 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467199 | ACGAATATTCATGTA[C/T]AAGCCTTCGTATGGA | 2074 |
rs550655445 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480430 | ATACCGGCACACAGA[C/G]TATCTTCTTAGAATT | 2074 |
rs550674343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459776 | CTACTGCTAAAAGCA[A/C]AGAACATGGGAAGTC | 2074 |
rs550699937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513788 | ATGGGGACTACAATT[C/T]AAGATGAGATTTGGG | 2074 |
rs550747080 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500960 | TAATTAGAGACTATT[G/T]CCTTTCTTTTCAACA | 2074 |
rs550754510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514269 | CCCCTGCAAACTTTT[C/T]CAAGTAACAGTAAAA | 2074 |
rs550762495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492857 | CCAGGCTTGTGCCCT[C/G]TCTGAGATGATTCGT | 2074 |
rs550772412 | snp | A/C | | | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49538999 | AAGGAAACAGAGACG[A/C]TACCGCCGCCAGCCG | 2074 |
rs550798539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538236 | CATTTGGAGGGTTGG[C/T]CGGACACAGGCACAG | 2074 |
rs550858500 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532066 | AACAAGGATGGAAGA[A/C]AAGAAAACCGGGGAG | 2074 |
rs550859881 | in-del | -/AT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527862 | TACACACACACACAC[-/AT]ACACACACACAATGA | 2074 |
rs550864123 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526179 | TGGGTATGCTAAGCT[A/T]TAGTAGACACTGTCA | 2074 |
rs550882859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486193 | CACATCCACAGCCTA[C/T]CCAGAGAGCTGACCA | 2074 |
rs550908624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501861 | GCTACTTGGGAGGCT[A/G]AGGTGAGAGGATTGC | 2074 |
rs551004388 | snp | C/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521701 | CAGTTCAGTGCAGAG[C/G]AGGAGGCAGGAGAAA | 2074 |
rs551009637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481891 | TCATGGCCCTCACCC[C/T]AGTGGTTCCTGCAGG | 2074 |
rs551015610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514433 | GGAATTATCAAATAT[C/T]AGTTGCCTGAGATCA | 2074 |
rs551092698 | snp | A/G | 3.39207e-05 | 0.00411816 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476319 | ATAAGACCTACGGAC[A/G]GGAAAAACAAGGAAA | 2074 |
rs551149050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517299 | TTAAAAATTACTAGT[A/C]TAGGATGTAGTGCAG | 2074 |
rs551182653 | snp | C/T | 0.000197668 | 0.00993955 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470357 | AGGCTTTTGCTTTGG[C/T]CTCAGATGTTTCTCC | 2074 |
rs551194914 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461266 | TGAAGAGAAATAACA[C/G]TATAAGCCTCCACAC | 2074 |
rs551277466 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539387 | CTCACAATTAACCTT[C/G]AACCCTGCAGAGAAA | 2074 |
rs551278969 | in-del | -/A | 0.0498117 | 0.149749 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455039 | GGTTCTTAAATAAAC[-/A]AAAAAAAAATGGAAA | 2074 |
rs551307480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496636 | AACATGGTGAAACCC[C/T]GTCTCTACCTAAACT | 2074 |
rs551307631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504627 | TGGTATTTGGCTTGT[G/T]TCTTAACAAAGAATC | 2074 |
rs551339481 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490650 | GAGCCACCACGCCCG[G/T]ACAATTTTCAAAATT | 2074 |
rs551398949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488635 | TAAGGAATAATGTGG[C/T]CTCTTTCTTTTTTTT | 2074 |
rs551430839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529579 | GCTTTGACCTTTGGG[C/G]TGCTATTCTGGAAGC | 2074 |
rs551444808 | snp | A/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455087 | TTTAAAACTTCCGTA[A/T]GATAAACATCACAAA | 2074 |
rs551566150 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528023 | TGATGCTTGGAAAGC[C/T]TGCCAAATACGCTCT | 2074 |
rs551580764 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463957 | AATGCACTAATAAAG[A/G]CAACTGGTACCAGTG | 2074 |
rs551724563 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457322 | CTCATTATATATAAA[A/C]CAAACTAAAAACAAA | 2074 |
rs551772094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500827 | AAACATGCGGGATGT[A/G]TGTTTTACATGAGTA | 2074 |
rs551829197 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526827 | AGACGGAGAGATATA[A/G]TAGGAACCAGGAACT | 2074 |
rs551895719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491789 | ATTGCCTTTATAAGA[C/T]AAACATCAGCTAATG | 2074 |
rs551896789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477308 | CAGAGGAAGAGGTTC[C/T]TGTACAGGATGGAGG | 2074 |
rs551944135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468262 | GCTGTCTCCGCTATC[A/G]TCTCTTGCATGTGAA | 2074 |
rs551959066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484477 | AGGCAAAGTGGCTTA[C/T]GTCTGTAATCTCAGC | 2074 |
rs551976290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478207 | AGAGAAGAATCCACT[A/G]AGGGCAGACGCCACA | 2074 |
rs551999331 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539288 | CGCCCCTAGCGAAAA[A/C]TACCCTGCTGGCAAG | 2074 |
rs552032272 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494001 | CATGCATTGACCCAG[A/C]AATCCCAATAAAAAC | 2074 |
rs552099159 | snp | A/G | 1.64917e-05 | 0.00287151 | missense | ERCC6 | GRCh38.p7 | 10:49472385 | ACTGACCGGTGGTAG[A/G]TCTTTTCTTCAATGG | 2074 |
rs552136095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471824 | TGGCTCAAGGATAAA[A/G]TCTGTGGTGGGGGAG | 2074 |
rs552196655 | snp | A/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517270 | AATAGCATAACTAGT[A/C]GAGAAGTTATTTCTT | 2074 |
rs552198369 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49505198 | GAGACTGAAAATGTT[C/T]CTCAGTATTTACATT | 2074 |
rs552203142 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498501 | GTACATATGAGCGGG[C/G]GGGACCACACTCCTC | 2074 |
rs552236895 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455620 | CATTTTAAACTGGTG[A/G]AGAAAAGAATATTTG | 2074 |
rs552295513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487186 | AAATCTGAAGGAACA[A/G]AATAAAGAGACATTG | 2074 |
rs552400537 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456134 | AATTGCTATAATAGA[A/C]TTCAAAAGACAGTAG | 2074 |
rs552407255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480687 | TGGCCAACACCACCT[C/T]AAAGTAATCAGAGTT | 2074 |
rs552445244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467883 | AGTAATTTTTTATTG[A/G]GTTCCAGACATTGTG | 2074 |
rs552505871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462063 | ACACTAAAGTTCATA[C/T]AGAACAATAAACCTT | 2074 |
rs552507706 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457519 | CTCTCTGAGTCACAT[A/G]GATGAGCAGACAGAA | 2074 |
rs552597727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509901 | TGCAGCCACATAAAA[C/T]GAAGTGGTGGGCATG | 2074 |
rs552625915 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540019 | TTTGTTGGTGGTAGT[A/G]GGTTTTTTTGTTTGT | 2074 |
rs552646672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523938 | TCGGGGGGGTCTAAT[A/G]TATTAAGCTGGATCT | 2074 |
rs552658415 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502609 | ATCGCTAGAAAAAAA[A/T]GAGCAAGCCAGAGCT | 2074 |
rs552671614 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458551 | CAAGGAGTAACTGTT[A/C]GGTACCTGATTTACA | 2074 |
rs552686309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496928 | TAATTTGTAGTTCTA[C/T]AGAAAAACAATGAAA | 2074 |
rs552719956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488956 | CGCCTGGCTAATTTT[C/T]TGTATTTTTAGTAGA | 2074 |
rs552732996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484148 | TAGCTGGATGTGGTG[C/T]CAAGCACCTGTAGTC | 2074 |
rs552755518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495024 | TGATACGTCCTACAC[C/T]GTATTCCCTGTCTGC | 2074 |
rs552784112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534027 | TAATCCCAGCCACTC[A/G]GGAGGCTGAAGCAGG | 2074 |
rs552987747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497478 | TGACTCACATTTTGT[A/T]ATCTAAGGCTAGTAT | 2074 |
rs552995509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504829 | CATCAAGTCACTTCA[A/C]ATCTTTAGAGTTTGG | 2074 |
rs552999349 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537746 | TTGAGACGGAATTTC[A/G]CTCCGGTTGCCCAGG | 2074 |
rs553003136 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524506 | TTTGTTTTTATTTTG[C/T]ACTGGGGCTGGAGGC | 2074 |
rs553003595 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503425 | TACTAGGCAGCATGT[A/G]AGTCATATCTCTAGC | 2074 |
rs553034439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504182 | TTGGCCCCGCTAAAA[C/T]GCAATCATAAAAGAA | 2074 |
rs553099392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471300 | TACATCAGTTAATCT[C/T]CCAGGTCTTGCAGAA | 2074 |
rs553112001 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498841 | AAGTGTGATGATAAT[A/C]GGAAGGGAAGCAAAG | 2074 |
rs553162095 | in-del | -/AT | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519241 | CAAAGGGAAGGAAAC[-/AT]GTATGTAGAGGGCCC | 2074 |
rs553185185 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465751 | GCCTGCTGCTATCCA[A/T]GAAAGATGTTACTTG | 2074 |
rs553237836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531810 | CTGCTCCATCCTCCA[A/T]CCCGTTCAGCCCTCG | 2074 |
rs553279359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511488 | GGAGTACAGTGGCAC[A/G]ATCTCAGCTCACTGC | 2074 |
rs553287025 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537903 | AATTTTTCGTATTTA[A/G]TAAAGACAGGGTTTC | 2074 |
rs553300565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471940 | AAACAGCCATCCTGT[C/T]GACTTCTTTGTAAGG | 2074 |
rs553333662 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478058 | CAGAGCCTAGGATCA[C/G/T]GACAGGCATATGGTT | 2074 |
rs553372727 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513565 | CTCACAATTCGGCAC[A/G]GCTGGGAGGCCTCAG | 2074 |
rs553375571 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538329 | CCACTCCCAGTGCAA[C/T]GGAATGACTCTGAAA | 2074 |
rs553419653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509054 | AGGCACAAAAGTCTG[A/G]GCTCAGACTAGCTAT | 2074 |
rs553419732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516096 | CCAGGGTGTGCCTCT[A/G]TAAGTGCCTCACTAA | 2074 |
rs553425755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488884 | CGCCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT | 2074 |
rs553461699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474574 | AATATAAAAAAGGAA[A/T]TCGCCTTTTAAATAT | 2074 |
rs553468305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465319 | ATGGCTGTACTTACC[A/C]AATGCCTGTAACCCT | 2074 |
rs553473684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460230 | AAGTGAATGTGCATC[A/G]TAAATCAGAGCGTGC | 2074 |
rs553526747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521825 | AAGGGCGACTGCCCA[A/G]TTCCATTAAAAAAGC | 2074 |
rs553588506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492567 | CAGATAAAGCTCTTT[A/T]TTGATACTGTGATAT | 2074 |
rs553636776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534161 | AAAAAAAAACAAAAA[A/C]AAAACTCCATTTTAA | 2074 |
rs553655351 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487116 | TTCTTAAAGAACTAG[A/G]ATTAAAATGTGTTTT | 2074 |
rs553798126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528684 | TTACTAGAGAGCCCT[A/G]TGTGAGCAACTACCA | 2074 |
rs553827475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468655 | TACACAACAAACACA[C/T]ACACACACATACATA | 2074 |
rs553863617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529216 | AGGTCAAGAATGTTT[C/T]AACTTCAAATACGAG | 2074 |
rs553888319 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455212 | CTATTATGAAATGTG[C/T]AAGACATTTATGAAG | 2074 |
rs553901554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462130 | ACACCCTATTGGACA[A/G]TAAAACACGCTCCAA | 2074 |
rs553963061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502181 | TAAATACGTCATAAT[C/T]AACTTTCTCCCAGTA | 2074 |
rs554096054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537809 | CTCACTGCAACCTCC[A/G]CCTTCCGGGTTCAAG | 2074 |
rs554127998 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455742 | CTAATAGGCAATGTA[C/T]GGTAGAGATCTACAA | 2074 |
rs554151992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495839 | GCCAGGTCCAGCCAC[G/T]CTCCTCTCTCATCTG | 2074 |
rs554191324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482310 | GATGCACTACCCCAG[C/T]TTGCAGGACTAAATT | 2074 |
rs554218268 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531064 | CTAGCTGATTTAGAT[C/T]AGCTCATTCCCATTT | 2074 |
rs554281513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499332 | CACAGAAGTATTGAT[A/C]TGCTAACTTAACGAA | 2074 |
rs554317505 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476660 | TGCCATGCTCTACTC[A/G]GCAGACCTGACCAGA | 2074 |
rs554381762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525150 | GCTCCGAAGTTCTCA[C/G]GTCATTGCTAAAACC | 2074 |
rs554414580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478590 | CAACAGCTGTATAAA[A/G]TCAGTGGGAAATGAT | 2074 |
rs554432747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479940 | GTGGAAAACAGACAA[C/T]TTGCTGAGCATGCCC | 2074 |
rs554433640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466681 | TCATGACTGTGTGTT[C/T]TCTAGAATTTTATGC | 2074 |
rs554477505 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496739 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 2074 |
rs554496848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460895 | CTCCATCTCTAAAAA[A/C]AGAAAAAAAAAAAGG | 2074 |
rs554510677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526235 | GTCCCCATCAACTGT[G/T]TCAGAAAGTTCCAAC | 2074 |
rs554591809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484859 | ATCAGACATCTTTTC[A/T]GCAACACTAAAAATG | 2074 |
rs554628599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492261 | AACACTCCATAGCCC[C/T]TGCAGCCGGCACTGC | 2074 |
rs554721950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472713 | TCTAGGAATGAATGC[C/T]ATGGATAAACTGCTG | 2074 |
rs554727741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487560 | AGTCTGCCCAGAGAA[A/C]AACCATCCACCTTTA | 2074 |
rs554753751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485338 | CCAAAGCTAGTACTA[A/T]TGACACTAGGCTACA | 2074 |
rs554759090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479314 | ATAAAAAAGAGCTTG[A/G]CCACACACACAGAAA | 2074 |
rs554764766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493840 | CTCACTACACCACCC[C/T]GCCTGCTCCTCTACA | 2074 |
rs554868233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513881 | TAACAATTAAAGCAG[A/G]CAGGGAGAAAGAAAG | 2074 |
rs554893111 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488323 | CGAAGCACAGGCACA[G/T]GAAGGCCATTCACAG | 2074 |
rs554899437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463569 | AAAATTATACATGTG[C/T]CTGCTTATTTCTACA | 2074 |
rs554908197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513322 | GTTTTGTTTTGAGAT[C/T]ACATATACACACATA | 2074 |
rs554939504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527664 | TTGGGCAACAAGAAC[A/G]AAACTCTGTTTCAAA | 2074 |
rs554994546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495968 | ACAGAGATTAAACAC[A/C]TGGACGTGGCCTACG | 2074 |
rs555089294 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49539014 | CTACCGCCGCCAGCC[G/T]CCTTGGAACCCAGCT | 2074 |
rs555137595 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539798 | CTCAGGATCGGTGCT[A/G]GGAGAAGGTGGACTT | 2074 |
rs555150406 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538061 | GAACACCGAATTTTT[G/T]ACTTTATTTTTAACT | 2074 |
rs555167667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496771 | TGAGATTGTGCCACT[A/G]CACTCCAGCCTGGGC | 2074 |
rs555167685 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490235 | GAGACTATTAACAAA[C/G]ATAACATAGGATCAA | 2074 |
rs555188560 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456614 | GAGGCAGACTATTGC[C/T]TGAACATTTTTAATG | 2074 |
rs555355606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523814 | AGACTTGCCTCCAAA[A/T]CCAACTAAAGACCTA | 2074 |
rs555392508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529932 | AGTAACAAATATTCC[C/G]TACCCTTAAGTTTTC | 2074 |
rs555405236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512395 | AGGGGCATGTTGCAC[A/G]GTTTGTCCCCTAGAC | 2074 |
rs555417879 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457486 | CAGTCCGGCAAGGCC[C/T]CCCTGCCCAGAACCC | 2074 |
rs555442203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518313 | TGTCCGAGTCTGCTG[C/T]AGCAAACCAAGCTGC | 2074 |
rs555480237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476873 | CAGTTACATTCCCAC[A/G]GATGCTCATTTAGCC | 2074 |
rs555520959 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489832 | TAGGTATCACAAGAC[C/T]GCCTTCTTTATCTCT | 2074 |
rs555555175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535738 | AGAAGTTTGGGGAAA[A/T]CTTCTAATAATAAAA | 2074 |
rs555631069 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537228 | GCGCGCCTGTAATCC[A/C]AGCTACTCGAGAGGC | 2074 |
rs555653297 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484607 | TAGCACTGCATGGTG[A/G]TGCACAGCTGCAGTG | 2074 |
rs555670723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497586 | ATTGGAGATTTTCAC[A/G]CTGAGTTGAGATCTA | 2074 |
rs555780821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520411 | ATAGAGTAAGAACTT[G/T]GGGGAATGAGTTTAA | 2074 |
rs555781122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526907 | AGAACCTAGGTGGCT[A/G]CAAAAGCCATGGGGA | 2074 |
rs555789691 | in-del | -/CT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535202 | GTCACAAAAATGAGA[-/CT]CTCAAAAAGGAAGCA | 2074 |
rs555865670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537409 | CTGAGAGTTAATTAC[A/G]CCAGGCAATGTACTA | 2074 |
rs555885904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471900 | TGTCTAAAATCCCCT[A/C]GTCATTATGGAAAGA | 2074 |
rs555889767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464831 | GGGAACTTCTGCCTA[C/G]ATTTCAAAAGATGTA | 2074 |
rs555952919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465226 | ATTTTGGAGCTTTAA[A/G]ATTTGACTGCCCTGC | 2074 |
rs555976852 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498401 | TTTTCTGTAAGACAT[A/T]AGTATAGAGAACTCC | 2074 |
rs556042498 | snp | A/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521981 | TATCCAGAAGTCACC[A/C]ACTCTCACTTCCTAG | 2074 |
rs556067138 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519236 | TCCCACAAAGGGAAG[A/G]AAACATGTATGTAGA | 2074 |
rs556084385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509005 | ATTCTGTATATAAAC[A/G]TCCTGGGTTTGACAT | 2074 |
rs556093044 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540183 | AGCTGGGATTACAGG[A/C]GCCTGCCACCATGCC | 2074 |
rs556162071 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455068 | AAGACTGAATTTACT[A/G]TATTTTAAAACTTCC | 2074 |
rs556196936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462116 | GAAAAGGCAAAGTAA[C/T]ACCCTATTGGACAAT | 2074 |
rs556281653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467365 | ACCCAACTGCTTCAC[A/G]TCTTTACCAACACTT | 2074 |
rs556324655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473779 | AATTCTTACTTTTGT[A/G]AACAGCCAAAGCTCA | 2074 |
rs556359782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508535 | AAAGGGCCAAACATT[C/T]ATTCAGTTTGGCTAA | 2074 |
rs556401181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534108 | CACTGCATTCCAGCA[C/T]AGGCAACAGAGTGAG | 2074 |
rs556435469 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454351 | CTGTGAGGTACCATA[C/T]CTCTGGACAGGGAGC | 2074 |
rs556468886 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469027 | GATCTAAAAATAAAT[A/T]AATAAATAAATAAGA | 2074 |
rs556483873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482250 | TCCCTGAACAGTCCA[A/G]TCCTCCTAGTGTCCC | 2074 |
rs556583645 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495077 | TGGGACAAAGGGACA[A/C/G]TGTCCCTTTTCTTGT | 2074 |
rs556636296 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469310 | TTGTAATAGGTCAAA[A/C]CAGCATGTGTCTCCT | 2074 |
rs556641108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536374 | AGGAGATAACCCAGA[A/G]AGGTGTACCAAAAGA | 2074 |
rs556658276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481845 | CCCCACCATCTTTCT[C/G]AGACCACCACCCAAG | 2074 |
rs556661582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491493 | ACCATATGTATGCAA[A/G]TGTCTGTGAAGGTAA | 2074 |
rs556755511 | snp | A/C | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457331 | TATAAACCAAACTAA[A/C]AACAAAAGAAATGAA | 2074 |
rs556781149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510289 | TAGAAGAATTTTCAG[C/T]ATTCCAAGGATGTTC | 2074 |
rs556838525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522429 | AATGTTAAGAGCTAT[C/T]GTATTTTGGTGGCAA | 2074 |
rs556842370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475874 | ATAATTCTGGTCATA[A/G]TATCTGGGAAAATGC | 2074 |
rs556850993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472103 | GCAGAAATATTCCTT[C/T]CAAATAACAATATGA | 2074 |
rs556857482 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507083 | GAAAGGGTAATACTA[A/C]ACATGCTGCCTGGCC | 2074 |
rs556898013 | snp | C/T | 1.65996e-05 | 0.00288089 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516328 | TGAAATATGTTTCAT[C/T]TGGAACAAATTTCAT | 2074 |
rs556916966 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479107 | TGAGTACTAAATATA[C/T]GCAAAAAAAAAAAGC | 2074 |
rs556964091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465375 | GCTTTTGATTTTACA[A/G]GCTCATAGGCAGAAG | 2074 |
rs556979472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498136 | TAAGCAATATGTTTC[C/T]CTGTCTTCTAGAAAC | 2074 |
rs556996913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499534 | TCTCCAAATCATATA[C/T]AGGGAGTGTCTGAGG | 2074 |
rs557002174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531006 | CAAATAAAACTTGTA[A/G]GATCATTAGAGGTTT | 2074 |
rs557018024 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497561 | GCCATTTTCCCCCTT[A/T]GTAGAAAAAATTGGA | 2074 |
rs557098613 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476078 | GCTGACTGCACATCT[A/C]CCATGCGGGACTTCA | 2074 |
rs557111372 | snp | A/G | 1.72288e-05 | 0.00293498 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493076 | TATGTAAAATGGAGG[A/G]CATTAAAACAAAACA | 2074 |
rs557147809 | in-del | -/ACT | 0.00398564 | 0.0444627 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540890 | CTCAGGATTTAGGGA[-/ACT]ACTACTTACTCTTCT | 2074 |
rs557153423 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460792 | CTGGCATGGTGGCGG[G/T]AGCCTGTAATCCCAG | 2074 |
rs557167937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537936 | CACGTTGGTAAGGCT[G/T]GTCTCGAACTCCTGA | 2074 |
rs557177818 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508274 | AATATTTTATATACA[C/G]GGTATCACTTTTTAA | 2074 |
rs557186681 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503026 | TTTTTGCTGAGATAC[A/G]GAACAACTGGACCAG | 2074 |
rs557209795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526460 | ATTTCTAGTTCTTTA[C/T]ACATCCTAGATTTGA | 2074 |
rs557238775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525124 | CTGAGTAGTCGTCCA[C/T]GAGGAAGCAAGCTCC | 2074 |
rs557274614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465878 | TTTATCAGCAGTGTG[A/G]AAACAGACTAACACA | 2074 |
rs557300388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525513 | GTGTAAAGTCACCAG[A/G]AAGTATCCCTCTTTC | 2074 |
rs557311144 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464909 | TCTCATGGAGAATCT[A/C]TCCTAGGGCAGTGCA | 2074 |
rs557441635 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468793 | TGAAGAAATGGCTGA[C/T]TCCAGGGCTGGCACA | 2074 |
rs557552971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503443 | TCATATCTCTAGCAG[G/T]ATCCCCAAAAACTAG | 2074 |
rs557607206 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469417 | GTGTGTGTGAATGAT[A/G]AAGCAAAAGCTGAAA | 2074 |
rs557625183 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540950 | TACGGCCTAGCAAGC[A/G]TACTGTTCACCTCTT | 2074 |
rs557643624 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503888 | TGGTGTACATTGGCA[C/T]TGCCACACTAACCCA | 2074 |
rs557650408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532354 | CTAACTACCATGTAC[A/G]ATGCCACTCCTAAGG | 2074 |
rs557674774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486648 | TCTGAACATTTTGAC[A/C]GATATGATAGCTAAA | 2074 |
rs557687404 | in-del | -/TTTAA | 0.00279162 | 0.0372561 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458076 | GTACCTACTTTTGGC[-/TTTAA]TTTGATTTTTTTTAA | 2074 |
rs557775731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523174 | CTATCAAGTATTTTA[A/G]AAGTAATAAGGTTCC | 2074 |
rs557786905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534668 | CTGCTGCTTTAAGGA[A/G]AATATATTCACTATA | 2074 |
rs557790717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510773 | GACACAGACAGAGAA[A/G]CGTGACTTGAAAATG | 2074 |
rs557809430 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490156 | GGTTGAAACTATCAG[A/T]TGTATATTTTTTTGC | 2074 |
rs557829590 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540310 | TCCTAGAGTTCTGGG[A/T]TTACAGGTGTGAGCC | 2074 |
rs557831797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463481 | GGCTGTCAGGATATA[C/T]GAAGTTTTTTTAAAA | 2074 |
rs557832376 | in-del | -/A | 0.00279162 | 0.0372561 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456833 | CAAGTCCCTCCAGCC[-/A]AGGAGGCACGGTAAC | 2074 |
rs557837239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523775 | ATGCCTCTTGCCCCA[A/G]CCTTCCCTTAAGTTT | 2074 |
rs557872636 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474897 | AATAATGGGGCTCTT[C/G]CAGCCTTGAGAGGAT | 2074 |
rs557944846 | snp | G/T | 0.00676609 | 0.0577691 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456478 | TTAGTAAAGGAAGAA[G/T]GGGAAAATGACATTA | 2074 |
rs557945357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517639 | TTTCTTTTTTTTTTT[C/T]CTCTCAGGCTCCAGT | 2074 |
rs557966935 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489058 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 2074 |
rs558016536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535369 | TTCCCAAGGCTCTGA[C/G]AGGTACCTAAGGTCA | 2074 |
rs558022176 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464259 | CAGGCGGCATTTTGC[C/T]CCTGCCCTAGAGATC | 2074 |
rs558100466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483203 | TAAAGAGTTTTCTGC[A/G]TTAAGGAAAATGCAC | 2074 |
rs558104160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511754 | CTAACTCCTAAAGCC[C/T]GTCTCAGGCTCCAGT | 2074 |
rs558137255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490605 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 2074 |
rs558138788 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491822 | TCCTGCCACAGGATT[G/T]TGCAGCACAAAACAC | 2074 |
rs558150009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476110 | GCAAGTGAAGTGAGA[C/T]GACAGTACGTGAAAA | 2074 |
rs558178522 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519751 | ACCAACAATGCTTCC[C/T]AACTGCCTCAAAGCT | 2074 |
rs558179290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525824 | CTCCCAGCCTCTACG[C/T]CCCCCAAGATAATGA | 2074 |
rs558181760 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457798 | AAAATAAACTGAGGA[A/T]CAAAGCAACACCATC | 2074 |
rs558190871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523734 | TGTCGGTATAAAGGC[A/G]ACACAGCTCACACTC | 2074 |
rs558242255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526365 | AGGTGCCTTTCATGA[A/G]TTTATCTTTTGGATA | 2074 |
rs558274645 | snp | C/T | 6.59098e-05 | 0.00574026 | missense | ERCC6 | GRCh38.p7 | 10:49470649 | TCTCCAAGCCTATCA[C/T]TGCTAGTTACATTAC | 2074 |
rs558287925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492999 | ATAAATTAACTTTAA[A/T]TGCAGGAAAAAAAAC | 2074 |
rs558315008 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494052 | ACTGGAGCATTCTTT[A/G]TACTGCAGAAAAAGT | 2074 |
rs558329249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512350 | GTGAGAAACCATACT[A/G]CAATCCTGACCTACC | 2074 |
rs558338364 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497457 | TTCTGCAAACTGCTA[C/T]ATTGATGACTCACAT | 2074 |
rs558374711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465673 | CTGTTCTTGTACTAG[C/T]GAATGAGTCTTATAT | 2074 |
rs558438429 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473723 | TTTAGGACAGATAAA[C/T]AGAACTGTTAAAAGA | 2074 |
rs558441808 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464743 | GTGGCTTCAGATGGT[G/T]CAAGCCCCAAGCCTT | 2074 |
rs558452706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504856 | TTGGCTTTCTATAAT[A/G]TTTAGTGGGATAAAA | 2074 |
rs558457913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460945 | GAGAACCACTCAGTA[C/T]CTTGTTCAAAAGATG | 2074 |
rs558569794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486543 | TGAGCCAAAATAACA[A/G]ACTGAGATGTACAGC | 2074 |
rs558591125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520346 | TGCTCGTTGCCCTCA[A/C]TGTAGTCTGCGAGGG | 2074 |
rs558605850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485410 | GATTGTATGTGATAT[A/G]CATACCATTTAAAAT | 2074 |
rs558615487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467341 | ACATTCCCACCAGGC[A/G]TGTATGAGACCCAAC | 2074 |
rs558649285 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454916 | GTAAAGGTGGCCTTA[C/T]ACATCAGGAGGAAAA | 2074 |
rs558724897 | snp | A/C/G | 0.000314127 | 0.0125287 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473053 | AGACACACAACACTG[A/C/G]GCACACACACTTAAG | 2074 |
rs558732469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480079 | GAGGGTCAACTAGGC[A/G]TCCCTGCAGGCTCTT | 2074 |
rs558749127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513998 | ATAATACTGTCTTCA[A/G]AAAAGTATTTTCCAA | 2074 |
rs558781633 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507815 | ACACAGGACAGCCCC[A/C]AAACCCCTCGGTAAA | 2074 |
rs558890748 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488541 | GTATACACTGACTCT[A/G]AAGTTAATAGGAATG | 2074 |
rs558894227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472706 | CCCCAACTCTAGGAA[C/T]GAATGCTATGGATAA | 2074 |
rs558979472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482954 | CTGCAAATTATTTAC[A/C]CATTTACTCATCATT | 2074 |
rs559105732 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477001 | TATGGTCAGTGCCGG[C/T]GCTGCTGGAGAAAAG | 2074 |
rs559193490 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511892 | AAGGGGAGGCCTGAA[A/C]TTTAGAAAATATAAT | 2074 |
rs559209312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521887 | AAGTATCAGCTAAAA[C/T]AAAGGCACCTAGTTA | 2074 |
rs559298949 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474261 | TGGTAAGAAAGAGTA[C/T]ATGTACACTCAGATG | 2074 |
rs559306653 | snp | A/G | 1.65072e-05 | 0.00287286 | missense | ERCC6 | GRCh38.p7 | 10:49476273 | ACGAAATTTTGGTAG[A/G]CTTTATGCTGCTCAT | 2074 |
rs559329821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517267 | CACAATAGCATAACT[A/G]GTAGAGAAGTTATTT | 2074 |
rs559331233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496084 | CCACCAGCCTGAACC[A/G]TCTTCCCTTCCTCCA | 2074 |
rs559355716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512496 | TTATATTTTTATAGA[C/T]ATTTTATCATTAAGT | 2074 |
rs559478004 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530525 | GTATGTGTGTTTTTT[A/T]AAATGCAATAGAATG | 2074 |
rs559482804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497193 | TTGAGCTCCCCAAGG[A/G]GAGTGGGACTCTGCC | 2074 |
rs559511402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533262 | AAAATCCTGGGGTGA[C/T]GGCCATGGAATATTC | 2074 |
rs559515698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529531 | TGTCCTCTCTCTGAT[C/T]TGGGAGGACCCACCT | 2074 |
rs559606554 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525188 | AGATGGACTTAAATT[C/T]AAGAGACAGTAAAAC | 2074 |
rs559607164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517839 | ATGAGCCATTGTGCC[C/T]GGCCAGGCTTATTTC | 2074 |
rs559649604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537260 | GGGGCAGGAGAATCG[C/T]TTGAACCCAGGAGGC | 2074 |
rs559718764 | snp | A/G | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540568 | CACTCAAAAGGGGAA[A/G]TTGAGAGTTATTATT | 2074 |
rs559755008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497768 | CCAAACAGACTACAA[G/T]TCCTTTAATCTTTGA | 2074 |
rs559758439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514879 | TGGTGTTTTACTTTT[C/T]TTATCTTCCTTTTTA | 2074 |
rs559759950 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508044 | GGAGTTTACATAATG[A/C]GAGAGTCCTCGGTAT | 2074 |
rs559793286 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536501 | TTTGCAGGTGGAAAG[C/G]AGGGAAGCTGAAGTG | 2074 |
rs559812888 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539224 | GTGCGAGCAGGGCGA[C/G]AAAGCTGTCTCCGCT | 2074 |
rs559821131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508597 | ATTGCCTGCAAGTAT[C/T]TGTATCATTGTGAAG | 2074 |
rs559826195 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536473 | CAGAAGGAGGATTCC[G/T]GATAGATCTAAATTT | 2074 |
rs559849669 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538817 | AAGCGGGCACTTGGC[C/T]CTAAGACCCGCTACA | 2074 |
rs559876248 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539672 | CCGTGGTGCGTTTGA[A/G]GAAAGAAGATGTCCA | 2074 |
rs559967001 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484455 | CCAAAAATAAATAAA[A/C]ACAGCCAGGCAAAGT | 2074 |
rs559988377 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454561 | TCTCTCTGTATGAGA[A/G]GAAGGTGTTTATTTT | 2074 |
rs560040122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533600 | CGAGCTCAGGACTTC[A/G]AGACCAGCCTGGGAA | 2074 |
rs560044892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484911 | CTTTACGTAATTCTA[A/C]GAAGGAAAAGTGGTG | 2074 |
rs560161948 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493453 | CATAATCTCATTCAT[C/T]AATTAGTGGATGTAG | 2074 |
rs560167716 | snp | G/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457290 | AAGTGACAAAAATAA[G/T]GTAATCATCTTCTTC | 2074 |
rs560198467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500768 | ATCATAACAGAAAGT[A/T]CTCATGAATTAATCA | 2074 |
rs560268924 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474925 | GATGATTCAAATCAA[A/T]CTCACTGGTCTAAAA | 2074 |
rs560287541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462876 | TCAAATTGATCTAAA[C/T]CTTACAAAAGGGAGT | 2074 |
rs560321213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461592 | AAAGTGATATTTCAC[C/T]CTGTATGCAAGAAAG | 2074 |
rs560324402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462407 | AAAACCATACAAGTA[A/G]TACAAGAAAACATGG | 2074 |
rs560332005 | snp | A/G | 0 | 0 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522073 | AAGGGTGCCTACCCT[A/G]GGAACTACTCCTAAA | 2074 |
rs560379234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521578 | ACCTGTATACCACTG[A/C]CCATAGAACCGACAG | 2074 |
rs560384735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487896 | ATTGTTCAAAATGTC[C/T]CAGTTGAAAATATAA | 2074 |
rs560420054 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527501 | CTAACATGGTGAAAC[C/G]CTGTTTCTACTAAAA | 2074 |
rs560430232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468376 | CTTTCTGTTACAGCA[C/T]GAAAATTCTCTCAAG | 2074 |
rs560445536 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456114 | TTACATATTTAAAGC[A/G]AACTAATTGCTATAA | 2074 |
rs560445608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481341 | CAAAATAAATTTTTT[A/T]AAAAAAAAGAATGGT | 2074 |
rs560447866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488749 | TAAAGAACATGTTGA[C/T]GGGAGTTTCATCGGA | 2074 |
rs560491680 | snp | A/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520659 | TGCCTATGATAGACA[A/T]CACTAAGGAACTGCA | 2074 |
rs560541646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509719 | TAAAAATTAGAAATG[A/T]CCTCAAAATGTCTAA | 2074 |
rs560543257 | snp | A/T | 1.65466e-05 | 0.00287628 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516470 | GTCACGTCTCATGGC[A/T]GCACTAACCAGTACA | 2074 |
rs560592811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495527 | AATGCCAAATCTAAG[C/T]CTCCAGCCCAGATCA | 2074 |
rs560645106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522540 | TTGTTTTACAATCTT[A/C]ACATTATTAAGAAAA | 2074 |
rs560700747 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510410 | TGTCCCCAAATCCTT[C/T]CCCTTACATATCCAC | 2074 |
rs560720190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465467 | GTTGAGACTTTAGGG[G/T]ACTGTTGGGAAGGCA | 2074 |
rs560735428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503674 | GGTTTTATTGCTTTA[A/C]CTTCCTAATAATAAA | 2074 |
rs560756655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465055 | AGCTTGCACCATGCA[C/T]CTGGAAAGGCTGCAG | 2074 |
rs560766038 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534403 | AGTCACACACAGGTG[C/G]AAGAATGTTTAGTGC | 2074 |
rs560813166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497797 | GATTACCATTGATTA[C/T]CTAATAAATTTAGGG | 2074 |
rs560815159 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467731 | TACCACACCCGGCTA[-/T]TTTTTTTTTTTATTT | 2074 |
rs560889428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484382 | TCTCCCAGAGTGTCA[A/G]GCAGAGACACTAAGA | 2074 |
rs560893826 | snp | A/G | 0.000345898 | 0.0131465 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524620 | CAAATACTTTTCGAA[A/G]CCTGATGCTTCATTA | 2074 |
rs560943318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485156 | CCTGCACCACATTCT[C/T]ACCACAGACCATGCT | 2074 |
rs560943574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492714 | TGCATACTAACAAAT[C/G]CATTTACCAATTAAG | 2074 |
rs560946426 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519261 | TGTAGAGGGCCCAGC[A/C/T]GACTTCAAATCTCAG | 2074 |
rs560946555 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512689 | CATATACACAATGAG[A/G]TATGTTGGGATGGGA | 2074 |
rs560966532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505655 | GAGGCAGGTCCATAT[A/T]GATTCATCAGTTTAC | 2074 |
rs560980442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492448 | CCGGGATATAAAAAT[G/T]AATCAGACACAGTCC | 2074 |
rs561109792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513018 | CGGTTCTCACAGACC[A/C]TCATTTCAAGCATCT | 2074 |
rs561203244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498996 | AACAAGCCAACCAAA[G/T]AGCTTATTTGAAACA | 2074 |
rs561239558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506317 | AAATTTCTCTGCTGG[C/T]TCGTAAGACATGAAA | 2074 |
rs561277829 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526621 | GAGTATTTTGCCTCA[A/G]TTAAGCCTTAGGTCT | 2074 |
rs561373688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494835 | ATCTAATGATTACAA[C/G]GACACCTGGCCTTAG | 2074 |
rs561391194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531900 | ATGATAAGTGAGCTC[A/G]ACCCCTCCCACTTCC | 2074 |
rs561439767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520453 | AACACTAACCCTAGT[C/T]CTGCCAGCAAGAAGA | 2074 |
rs561475138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473293 | AACATACACATGCCC[A/G]CAATCCCCGCCCCCA | 2074 |
rs561519544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472887 | ACTAATACATTCTTT[A/T]AAAAAAAAAATAAAA | 2074 |
rs561554572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479733 | AGCATGCTGGTTGGA[A/G]GTGCTGGTCAACTAA | 2074 |
rs561616372 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528819 | TTAAATACATGGGCA[C/G/T]TGACCTGAAAGGTGG | 2074 |
rs561644512 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480087 | ACTAGGCGTCCCTGC[A/C]GGCTCTTCTCAGTTC | 2074 |
rs561660108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523249 | GGAGACTTGAAATGC[A/G]CGGCAGTAGCACAGT | 2074 |
rs561661145 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523439 | CAAAGTCAGTCTCTA[A/G]CATAAAAAACAACAG | 2074 |
rs561679305 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456032 | ACAGGAATAGAAATG[C/T]CTTGCATATAATATT | 2074 |
rs561687766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533861 | AAAATAGGCTGGGCA[C/T]GATGGCTCACATCTG | 2074 |
rs561758503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482434 | GCCAAAACTGTTTAA[A/T]TTCCATTAAACAAGG | 2074 |
rs561872586 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529352 | CTCTGAATAGTCTAC[C/G]TCTAACCATCAAAGA | 2074 |
rs561906771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482925 | AATCGCCATTCCTAC[A/C]CTAAAACGCTCCTCT | 2074 |
rs561909917 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536117 | GTGAAACTCTGTCTC[A/G]AAAAAATAAAAAAGT | 2074 |
rs561927841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513858 | TCTCTCTCTCTCTCT[C/T]TTTTTTTTAACAATT | 2074 |
rs561983430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511119 | GCTCCATTTTTTGGG[A/T]TCATCACCAGTAGGT | 2074 |
rs562012735 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485915 | GGTAAGGCAAAAACC[C/T]AGCCTTCTGTTTAAA | 2074 |
rs562070360 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536426 | CAAGCAGAAATGAAC[A/T]GGAGGCACAACACAT | 2074 |
rs562129990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496249 | GCACTCCACATTAAC[C/T]CTGACAAAACACAAA | 2074 |
rs562144953 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481601 | ATGCACAGAAACCGT[C/G]CCTCCCACCCAGGCT | 2074 |
rs562149691 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501305 | ATTACTAGCAGATGC[-/A]AAAAAAAAGCACAGT | 2074 |
rs562191634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464428 | ACAATTTGCAGCCTT[A/G]CAATGTGATAGGAAA | 2074 |
rs562204400 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483782 | TACATATATTAAATT[A/T]TTATTTTTATTTTTT | 2074 |
rs562204481 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457893 | GAAACAAGAAAGCCC[A/G]TCGCAAGGAATGCAA | 2074 |
rs562264382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490941 | CGCTGAGTTAGAGGA[C/T]GAATCACCACAAACA | 2074 |
rs562296066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497112 | GGCTACAAGAGACTC[C/T]GACACTCTTCCTACA | 2074 |
rs562307737 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538733 | CTGGGTCGCTGGCCG[G/T]CCAGGGACTCAAGCC | 2074 |
rs562329360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491536 | AGGTAAAGCCACTGC[A/C]ACCAAAAGTGAAATA | 2074 |
rs562332786 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510705 | CTCCTCATGGCAGAC[C/T]GTTAAGTGCTGAATG | 2074 |
rs562397144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530490 | GGAGCAACTGTATAC[A/G]TATGGATGTGTGTGT | 2074 |
rs562407917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507832 | AACCCCTCGGTAAAA[A/G]GTTATCAAGTCTCAA | 2074 |
rs562436615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461081 | TTTAATCATTATCCT[A/G]TATCTCTTACTATTT | 2074 |
rs562534485 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490644 | AGGCATGAGCCACCA[C/T]GCCCGGACAATTTTC | 2074 |
rs562673066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493333 | AGATCCCCCAAAACA[A/G]CAAACAAAAAACTTA | 2074 |
rs562695003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527351 | ACTGGTCATAGGCCT[A/G]ATGAATTCTGAGAGG | 2074 |
rs562697922 | snp | C/T | 4.94866e-05 | 0.00497402 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49500630 | CAATCCCATTTCATC[C/T]CCCAGAATTCCTCCT | 2074 |
rs562722427 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493896 | CCGAGCGAGTGTTCT[A/C]TCCTGGGAAGCCCAC | 2074 |
rs562744042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474847 | AGGGGTGAGTGCCCC[A/G]GCCCATCCCCACAAA | 2074 |
rs562746072 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467730 | GCTACCACACCCGGC[C/T]ATTTTTTTTTTTATT | 2074 |
rs562753780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487830 | GTGTTCAGGAAGATG[C/T]ATTAATGATTAACAA | 2074 |
rs562763489 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486864 | CAATCATTGTTACAA[A/G]GCTAGCAAACCCTGT | 2074 |
rs562789375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526721 | CGGAGATGAATTTCA[A/G]CTAATGAAAGAGGGA | 2074 |
rs562827992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524957 | TATAGCATCATGCTA[C/T]ATTTAATATATTCCT | 2074 |
rs562828066 | snp | C/T | 4.94344e-05 | 0.00497139 | missense | ERCC6 | GRCh38.p7 | 10:49532600 | ACGAGCTGGGAGGCA[C/T]GGCTGGCCTCATGGA | 2074 |
rs562847786 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467111 | CATATGGATATGCCA[C/T]GGTTAGTTTAACTAT | 2074 |
rs562924198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480522 | CCAAAGATCTCACCC[A/G]CTAGGAAGGGGAGAA | 2074 |
rs562947169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49515022 | CCAAGAATGAAAGGT[A/G]TGTGCAGAGCAGGAA | 2074 |
rs562951189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521992 | CACCCACTCTCACTT[C/T]CTAGAGTTGAAAAGA | 2074 |
rs563005835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502409 | GAAGAAGGACAAATT[C/T]CGAAAATATGTGGTA | 2074 |
rs563034452 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455459 | AGACACTGAAGAGGG[A/G]GAGAAAGGAAAAGGA | 2074 |
rs563040677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509309 | TTCTGAAATCCTCAC[A/G]ACAACCCTGCAGCAG | 2074 |
rs563066133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461836 | ACAGAAAAGACCAAA[C/T]ACTTAGGAATAAACC | 2074 |
rs563068620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462301 | GATGCTACAAACGTT[A/G]GGGCACAAACGTTGG | 2074 |
rs563136926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508705 | TCAGGCGAAGAGATT[C/T]TTCTGTTACATAAGC | 2074 |
rs563141393 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500819 | AGTCAGAGAAACATG[C/T]GGGATGTGTGTTTTA | 2074 |
rs563142074 | snp | C/T | 3.30028e-05 | 0.00406205 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470837 | TGCTCCAAAGGCTGG[C/T]TGAATCCTTCTTTTT | 2074 |
rs563153388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483001 | ACTCTCCAAAACATA[C/T]ACATTTTATGCAATT | 2074 |
rs563290307 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498337 | AAATATACATAGCCA[A/T]TGAGGCAATAACAGC | 2074 |
rs563307808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464550 | GGAAAATGTCTGCAG[A/G]GCATATCAGAGACCT | 2074 |
rs563310732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490831 | GTCCCAATGTCAGAG[C/T]ACCATTATTAAATTC | 2074 |
rs563356062 | snp | A/T | 0.000197661 | 0.00993939 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524551 | AGCTTTTCTAGCTGC[A/T]CTTTTATTACAACCT | 2074 |
rs563393827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492364 | GCTGCTTCTCCCCAA[C/T]AATGTAACCTGCAAA | 2074 |
rs563403531 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473745 | GTTAAAAGAGTATTT[C/T]TGGTATTTCCGTATG | 2074 |
rs563484923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459395 | AAAAGGGAAAGGAGG[A/G]GGGTCTGGTATCTAA | 2074 |
rs563521533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518606 | CTTTGCTCAGGCCCT[A/G]AAGGCTGCAACGTTC | 2074 |
rs563557833 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501993 | ATGATGCAAGATAAG[C/G]CATTTTTTTTTCAAA | 2074 |
rs563569979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506114 | ACAGGCAAATTAGAA[C/T]GGTCTCTTAGGTTAA | 2074 |
rs563571807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505568 | AATTAGGAGTTTGGC[A/G]CCTTAAAATTACTAA | 2074 |
rs563726963 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508866 | CATCTGCACATACAC[A/G]GAAACGTGCCTTCCT | 2074 |
rs563734337 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502328 | ACTGGATATGCACCT[G/T]GGAGAAAAGAACTAA | 2074 |
rs563773203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501791 | TAAGACCTCATCTCT[A/G]CAAGAAAAAAAAAAA | 2074 |
rs563833311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537374 | AGAAAGAAAGAAATC[A/T]TACATTTAACAAATA | 2074 |
rs563864839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479706 | ACCCACACCCCCTTC[C/T]GCAGAAGAGCGAGCA | 2074 |
rs563884033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478940 | TGGGGAAAAGCTACA[C/G]TGATGGAGCAGCCAG | 2074 |
rs563900348 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477620 | CTTCACTTCTGTTCA[G/T]GCACCTGTCTGTGCC | 2074 |
rs563978977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494677 | TACTCCCCTGAAACT[C/T]TCACTAGTCCATGAA | 2074 |
rs564010970 | snp | C/T | 6.59348e-05 | 0.00574135 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472405 | TTCTTCAATGGTGCC[C/T]GCAGTCAGGAGCCTG | 2074 |
rs564021638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533747 | GATGGAGGCTGCAGT[A/G]AGCCATGATTGCACA | 2074 |
rs564042565 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504681 | TGCCAATAAAAGTGG[C/G]CTTTATTTACCTTTC | 2074 |
rs564058472 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539750 | AGAAGCAGCCCACGA[C/T]GCAGGATGGCTGTAC | 2074 |
rs564081776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462237 | TTTGGAAATGTACTA[C/T]ATGATAAAGGCATCT | 2074 |
rs564205010 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455343 | TTATTCTCAAATTAA[A/T]GTGTAAACAAATGCA | 2074 |
rs564263211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534249 | ATCCAATACAGACAA[A/G]GAGAAGGATCCCCCC | 2074 |
rs564293219 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456848 | CAGGAGGCACGGTAA[C/T]AATGTGTCAGATCTC | 2074 |
rs564318678 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487240 | GTAACATTCAAAGAG[C/T]TAATACAATTGCTGC | 2074 |
rs564372879 | snp | A/G | 1.65392e-05 | 0.00287564 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516536 | CCTTCTAGGAACTGA[A/G]ACATAACCACTCAGA | 2074 |
rs564433089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510510 | CAGACTTAGGTGTCC[C/T]GTCTTCCAAGGGCCC | 2074 |
rs564449499 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463009 | TGTGGCTAAAAGAAG[C/G]TATAAAAAATCTAAA | 2074 |
rs564478537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475615 | GAGAAGACACTAGCT[A/G]GGAACTTCTGAATTC | 2074 |
rs564506854 | snp | A/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520110 | TATACAAACTGCATC[A/C]GCCAAAAGCTGCAGC | 2074 |
rs564545836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503250 | AGGAACCTGAGAGGG[G/T]GTTAAGACAACTAGA | 2074 |
rs564578974 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511096 | TTGTGTGAGTGATTT[A/C]AGTCTGAGCTCCATT | 2074 |
rs564588075 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49493323 | ACTGCTCAAAAGATC[C/T]CCCAAAACAACAAAC | 2074 |
rs564594987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463723 | CTACACTGTTCTCAT[G/T]AGTGAATGAGTTTCA | 2074 |
rs564651198 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49483259 | ACAAGGAAAGATTCA[A/G]TAAATGTGTTACTAA | 2074 |
rs564668605 | snp | C/T | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496196 | CAAAGCCTTCCCTGT[C/T]CCTTTCTCTGTAAAC | 2074 |
rs564705309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503776 | ATATAAAAATTACTC[G/T]TTAGGGACAGTTAAA | 2074 |
rs564737006 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495239 | AGAAGTCAAAACTAA[A/C]CGTGGCAACCTCTTC | 2074 |
rs564749302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459654 | AACAATATCATAGCT[A/G]TACTTCCTTTTCTTC | 2074 |
rs564773304 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460790 | GCCTGGCATGGTGGC[A/G]GGAGCCTGTAATCCC | 2074 |
rs564794025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535988 | AGGCGTGGTGGTGCA[C/T]GCCTGTAATCCCAGC | 2074 |
rs564836870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519847 | TCCCCTCAGAGTCAG[A/C]GGGAGCTCAGCCAAA | 2074 |
rs564875772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472809 | CAAAATGTGAAACGT[A/G]TGCTGAAGCCAACCA | 2074 |
rs564881072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472373 | GCCACTGTGTGCACT[A/G]ACCGGTGGTAGATCT | 2074 |
rs564939414 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519354 | GTAAAGATGTGTATT[C/G]ACAGAACCAAAGACT | 2074 |
rs564943064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466107 | ATAAATTAACCTAAC[C/T]GTATTTTAAACTGAT | 2074 |
rs565040013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465512 | ATGTGAAGATATGAG[A/G]TATGGGAGGGGCCAG | 2074 |
rs565068597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499732 | TTAAATATGGAAGTG[C/T]TCATAGTACTTTCTT | 2074 |
rs565069992 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492958 | ACTGTTCTGAAAACA[C/G]AGAGCTCTAAAGTAA | 2074 |
rs565079376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480404 | ATTTTAGCACCAGCA[A/T]GACAGAATAAATACC | 2074 |
rs565115087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486794 | GTTTTATGAGTAAAG[C/T]AGGACTAGATCCTAT | 2074 |
rs565134636 | snp | C/T | 1.65206e-05 | 0.00287403 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500487 | CAGCAATACATCTGA[C/T]GAAATATTAATTGAG | 2074 |
rs565141793 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492822 | CGCAGCCACCTGACT[A/T]ATGACTCCAACCCAC | 2074 |
rs565142205 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473328 | TCCAGAAGTAGGGCA[C/T]AGAGTTAAAAACAAC | 2074 |
rs565211335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508639 | CAGTAGAATTATACA[C/T]ATATTAAAGACAGAA | 2074 |
rs565276743 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467000 | TGTCCAGGTTGGTCT[C/T]GAACTCCTGACCTCA | 2074 |
rs565297276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486059 | AGGAGTGAACAGAAA[A/G]AGGGATATTTTATAT | 2074 |
rs565353918 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482022 | AGCCCTCCCTGAGTG[C/T]CACTGCTTCCCTTTC | 2074 |
rs565359307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527124 | AACAAGGATAAAAAG[A/G]GGCTCTTGGATTTGA | 2074 |
rs565501573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498840 | TAAGTGTGATGATAA[C/T]AGGAAGGGAAGCAAA | 2074 |
rs565522767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514286 | AAGTAACAGTAAAAT[C/G]AGTTTAGCAGTTCTT | 2074 |
rs565582666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510657 | CAAACACTGTCTTAG[C/T]CATTTTTATAGCACT | 2074 |
rs565610894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503961 | TGAAGTTTGTCATTT[A/G]ACTGCTAAATTAGAT | 2074 |
rs565645119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511188 | TGGAAAGAACCAGGA[A/G]CCCTGAGTTTGCTCC | 2074 |
rs565645409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503420 | AATCTTACTAGGCAG[C/T]ATGTAAGTCATATCT | 2074 |
rs565662180 | snp | C/T | 0.000133198 | 0.00815973 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516128 | CTGAAGGACAAGTGA[C/T]GCACCGACACCATAT | 2074 |
rs565727472 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49505442 | ACCCTCAGGTACAAT[A/G]TAAGACACTCAAAAA | 2074 |
rs565727863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475790 | GTTCATAAACATTTA[C/T]TGGGGAATGGGGCTC | 2074 |
rs565743411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534621 | GGAAAAATAAGGGGG[A/G]ATGTTCACATTGTAC | 2074 |
rs565749947 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516670 | CCTCGTCATCAAGAA[A/G]AAGTTCAAGAATTTC | 2074 |
rs565792494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522828 | AAACGTGCACAGAAA[C/T]GAAAGCTGTGCTGAG | 2074 |
rs565808141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495866 | TCTGGGTTACTGCAT[C/T]TCCGAGGATGATTAT | 2074 |
rs565829726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530243 | GGAACTTTTCTCAAA[A/T]ACACAGATGGTCTCC | 2074 |
rs565869331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529808 | ATTCCTATCTATTGC[A/C]ATGTATTTTCACAAA | 2074 |
rs565950484 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537682 | TCAGTCAGGTCGAAA[-/G]TAAAGTGAACGTCTT | 2074 |
rs565995371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491009 | TGTAATTTAACACAC[A/G]TGTAAGCCAGCAGGT | 2074 |
rs566027784 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456355 | TTCTTTAAAGGGCCA[A/G]TTGGGAAGTTTAAAA | 2074 |
rs566098875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496513 | AATTATTCCTGAACT[C/T]AAAACAATTTTTGGC | 2074 |
rs566149344 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511323 | TTACTAGGAAGGAAA[C/T]AGTGTTTTTGATGTT | 2074 |
rs566151225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464069 | GGAGGGCTCAGAAGA[C/T]GAGAGGAAAATGTGG | 2074 |
rs566229285 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518766 | GGGCCCTGGCCACAG[A/T]GGCCCAGTGCTCAGG | 2074 |
rs566266343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532133 | GCCCAAGGACTGAAC[A/G]CTAAGTTTGGGGACA | 2074 |
rs566295150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476755 | GACTTGCCTTGGACG[A/G]CAACCCTTACCCTCC | 2074 |
rs566385917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518240 | GATAGGAATGGGACA[C/T]TGGGTTGGAGTTGGC | 2074 |
rs566388588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499937 | ATAAAGTTCATAGAT[C/T]GGGAAGGGCAGAAAA | 2074 |
rs566482119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460636 | TCCTAGAAAGTAACT[A/G]CTGGCTGGGCGCAGT | 2074 |
rs566488231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511574 | GGACTACAGGCATGC[A/G]CCACCATGTCCGGCT | 2074 |
rs566504435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492561 | GGAGCACAGATAAAG[C/G]TCTTTTTTGATACTG | 2074 |
rs566509813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526763 | TGACTTTACAGTTAT[C/G]GTGTAACTTCCAATT | 2074 |
rs566542781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486425 | GGAAAATGAGAGAAT[C/T]AGTAAGATAAAAATT | 2074 |
rs566551107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467287 | CAAGGAAAGCGCATG[A/C]AACTGCCAAACTGTT | 2074 |
rs566562432 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526310 | TGTAGTGGTACCACA[C/T]TATGGCTATAATTTA | 2074 |
rs566668545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480631 | CTATAAATGACTTAT[C/T]AATGCCAAAGGAGAA | 2074 |
rs566673364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520829 | AACCTCCAAGGCAAT[A/C]CAAATGAGAACCCTG | 2074 |
rs566690778 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498498 | CTGGTACATATGAGC[-/G]GGGGGGACCACACTC | 2074 |
rs566697477 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455529 | ATGACAGCGTGAGGA[A/G]TGTGGTTGGTAGAAC | 2074 |
rs566705367 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487034 | CCTAATATAATTCAT[A/G]TAATCACAATCATCT | 2074 |
rs566733220 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454861 | CCAATTTAACAGAAT[A/G]CAGAGCCAAGAAACA | 2074 |
rs566754675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514717 | TCAACAACAGAGGCA[C/T]AATGAGTACAATTTG | 2074 |
rs566780471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488939 | CAAGGTGCCTGCCAC[C/T]ACGCCTGGCTAATTT | 2074 |
rs566799495 | snp | C/G | | | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515153 | TTTTTTGAATTTTTG[C/G]ATGAAATTCATATAT | 2074 |
rs566801487 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461816 | GGAAAATTCTATTTA[A/C]AGTAACAGAAAAGAC | 2074 |
rs566840578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490300 | GGGGAAGAAGAATGA[C/T]AGATGTGCTTAATTG | 2074 |
rs566844971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467811 | TAGGCTCAAGCAATC[A/G]ACCCACCTCAGCCTC | 2074 |
rs566904880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464154 | AGTGATATGAACAGT[A/G]AGGTCCAAACTGAGG | 2074 |
rs566909606 | snp | A/G | 3.30677e-05 | 0.00406605 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470913 | AGGAAAAACACCACT[A/G]ATACTATATTGTATC | 2074 |
rs566918236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49515082 | TTTGTTATTTAAAAG[A/G]AGGCAATGTGCTCTC | 2074 |
rs566918269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508377 | ACATCACTCTGCATC[C/G]ACAAGATTCAGTTTC | 2074 |
rs566920571 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458796 | AAAAGGGACTTGAAA[A/G]TTTAGGAAGCAATGT | 2074 |
rs566939054 | snp | C/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521226 | AATCAATAACATGGA[C/G]GTAACAAGGACTGGG | 2074 |
rs566959735 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | ERCC6 | GRCh38.p7 | 10:49539483 | CCCACGACTGAACAC[C/G]GGAAGGATGGAGAGC | 2074 |
rs566977108 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508806 | GCTAAAGATGGGGCC[A/G]ACAAGTACACCACAA | 2074 |
rs566983582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494281 | TTATAGGGTTATTAC[A/G]AAGATTAAATCAGTT | 2074 |
rs567012099 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533198 | GAAAAAGAAATGCAG[C/T]ATCATCAACAAAGGA | 2074 |
rs567027282 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539961 | CTCCATAACATCATC[A/T]TATTCCTCCTGTCAG | 2074 |
rs567051758 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491617 | ATTTACTGTCAATTC[G/T]ATTTCCATAATGAGT | 2074 |
rs567191757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484112 | GGTGAAAGCCTATCT[C/T]TAAAAAAAAATTTTA | 2074 |
rs567204488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533929 | ACTTAAGGTCAGGTG[G/T]TTGAGACCAGCCTGG | 2074 |
rs567225009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518026 | CAACCTCCACATTGT[A/G]AGTTGGCCTTTGCCG | 2074 |
rs567230459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491320 | TTACATCTTTAGTGA[C/T]CTAAGATACTTTATA | 2074 |
rs567357436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484521 | GAGGGAGGAGAATCG[C/T]TTGAGGCCAGGAGTT | 2074 |
rs567385629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512035 | CAGATGCTATAACAG[C/T]TGGCAGATTACACAA | 2074 |
rs567406552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512833 | TGAGACCCAACATAT[A/G]AGGTCAAATATGGAA | 2074 |
rs567441070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536283 | CTACAGTGATAAAGT[A/G]ATAATGGATTTGTTG | 2074 |
rs567488389 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497968 | ATGATATCCAAGACT[A/T]TAAAAAATTAACTGA | 2074 |
rs567545618 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533075 | GATTTCTCAAAAGAT[-/C]AAGTAATAATCTTCC | 2074 |
rs567548745 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49530768 | TTTCCTGTTGATGTC[C/T]CTGCTGGTGGCAGCT | 2074 |
rs567566496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513183 | ATCCCCATCTTACAG[A/G]TGAGTGGATACACAA | 2074 |
rs567603713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537000 | GTCTTCTGGAAGTGA[C/G]AGTTGGAAACCAGAA | 2074 |
rs567605418 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529282 | CACTGCAATGACTTG[A/C]AATTTGTTTTTTCTC | 2074 |
rs567610495 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524951 | TAAAATTATAGCATC[A/T]TGCTATATTTAATAT | 2074 |
rs567646632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459586 | CCACTTTCAGTACCT[A/G]TGGGCTTTTCCTGTT | 2074 |
rs567676918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525353 | TTGCATTTGCCCTTT[C/T]TCAAGTGCTCAAGAG | 2074 |
rs567708812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471908 | ATCCCCTAGTCATTA[C/T]GGAAAGACAGAGGAC | 2074 |
rs567847626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465683 | ACTAGTGAATGAGTC[C/T]TATATGAGATCTGAT | 2074 |
rs567853640 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471897 | CACTGTCTAAAATCC[C/T]CTAGTCATTATGGAA | 2074 |
rs567864286 | in-del | -/ATTATT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474735 | TCCATTTACCTTTAG[-/ATTATT]ATTATATCAGAAAAA | 2074 |
rs567882036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465236 | TTTAAGATTTGACTG[C/T]CCTGCTGGACTTCAG | 2074 |
rs567953619 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477790 | AAACCTACAAGACTT[A/G]CTCCTTCGCCTTCTT | 2074 |
rs567989806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499033 | GCATTTTATTTGAAA[C/T]AGAAAAAGCATATTA | 2074 |
rs568008142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460078 | GGAGCTGGCACTTTC[C/T]CTCTAGACAAGGCAG | 2074 |
rs568088052 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540826 | TTTATACTCCTGCCC[C/T]ATCTAATTTTTCTGC | 2074 |
rs568106052 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481509 | AATACTCCAAAATAC[A/G]AGAGCTTCCCTTTTG | 2074 |
rs568115736 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537067 | AAATCATACATTTGC[C/T]GGGAGCGGTGGCTCA | 2074 |
rs568245039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468640 | ATGTGTATATGTATG[C/T]ACACAACAAACACAT | 2074 |
rs568251866 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534517 | GTATGAACACACTTA[G/T]GCTGAAAAAAGTATC | 2074 |
rs568281946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468040 | ACCCAATGCCCCATG[A/G]AATATTTTTCCAGTC | 2074 |
rs568316510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535086 | ATGCATGGTCTGATA[C/T]ATAGGAGGTGCTCAA | 2074 |
rs568368639 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455655 | TCATTGGAATAACTG[C/T]CTTTTTGTTTTTGTT | 2074 |
rs568411179 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462498 | GACTGACAATTTTTT[A/T]AAAAAAAAACCTGTT | 2074 |
rs568413077 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456248 | CCTCAACACATCACT[A/T]CCATCTCTTGAGATG | 2074 |
rs568509273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495091 | AGTGTCCCTTTTCTT[G/T]TTTGAGACCAATCCC | 2074 |
rs568520317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523095 | CCAATAAATACAACA[A/G]ACTAGGTCTCTTCAC | 2074 |
rs568556702 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475906 | GCTATGTACCTGACA[A/C]CCGCCCACCTACCAG | 2074 |
rs568637238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483082 | ATTGTTGAAGCTGAA[A/T]ACTATAGATTAGAGT | 2074 |
rs568705667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490353 | TTCCAAATGAAAAAT[C/T]TTCCTTTTTTTTTTT | 2074 |
rs568725651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459816 | CTAGTATTCCTAAAC[A/G]TGTTCACATTAACTT | 2074 |
rs568762155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517410 | CCAGTATCTGTAGCA[C/G]TAACTAACTCTGTGC | 2074 |
rs568765193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465641 | TGACTGAATTATGGG[A/G]TTGGGTCTTTCCTGT | 2074 |
rs568800181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506634 | TTACAAATTTAGTAA[C/T]ATGATACTTTCAGAT | 2074 |
rs568838614 | snp | A/C | 0.000131878 | 0.00811922 | missense | ERCC6 | GRCh38.p7 | 10:49459193 | TCTTCCACTAAAATG[A/C]TCAGGGACATTATCT | 2074 |
rs568894810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466642 | GTCAAATACCCCATG[A/C]CCAGACAACCAATCC | 2074 |
rs568910243 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498344 | CATAGCCAATGAGGC[A/C]ATAACAGCTCACACA | 2074 |
rs568933083 | snp | G/T | 9.91195e-05 | 0.00703917 | missense | ERCC6 | GRCh38.p7 | 10:49472972 | GTTTGCCCCCGTCAG[G/T]TTGACACCTAAGCCG | 2074 |
rs568956558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486275 | GGATGCAAAGGATTT[C/G]AGTATCACCATCAGA | 2074 |
rs568968744 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499284 | ATAAATGCAACTGGC[A/G]TTCTAAAATATTCTA | 2074 |
rs568974289 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537765 | CGGTTGCCCAGGCTG[A/G]AGTGCAACCTCCGCC | 2074 |
rs568984944 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467195 | TGCTACGAATATTCA[C/T]GTACAAGCCTTCGTA | 2074 |
rs569007339 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472324 | TTTGGAAAAATTCCC[A/T]GCTCAAGACTCTGGG | 2074 |
rs569029875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479213 | AAAAATCTAAATAGG[A/C]TTAACAACTTAGTAA | 2074 |
rs569033832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531692 | CTGAGGAGGCCAAAA[A/G]AACACACCAGGGAAT | 2074 |
rs569070568 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485320 | GGAGAAAGGCAGCCA[A/G/T]ATCCAAAGCTAGTAC | 2074 |
rs569181660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494215 | CACACCATTTAACCT[C/G]TGGGAACGTCAGTTT | 2074 |
rs569231909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520699 | CAATCCACCCAAACA[A/G]GGCCTCGGAGCCCCC | 2074 |
rs569285180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476430 | ATTTTAATGATATCC[C/T]TATTATTAATATTAA | 2074 |
rs569287064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469910 | GCCTACTAATGTTCA[A/G]GTAGTACACATCGAT | 2074 |
rs569356037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461296 | CCTGCCCTGATTTTA[C/T]TTCTAGCCTTAGTTG | 2074 |
rs569379516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460864 | ACTGCACTCCAGCCC[A/G]GGCGAAAGGGCGAGA | 2074 |
rs569390551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500976 | CCTTTCTTTTCAACA[C/T]TAGAAATAGCTTGCT | 2074 |
rs569449792 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538938 | CCCCTGCCCGACATT[C/T]GGCCGGGACCCCCGA | 2074 |
rs569503220 | snp | C/T | 3.2962e-05 | 0.00405954 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516745 | TAACTCTACCTGCTA[C/T]GGGTTGTACAGTTAG | 2074 |
rs569506860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487504 | CCTCAGGACTCCCTC[A/G]CCACCAGCCCCACTT | 2074 |
rs569553519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504048 | ATCTTGCAGAAAATG[C/T]ACTTAAATGGCTAAT | 2074 |
rs569564278 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454796 | GATAATCAATTATGA[C/T]ACCACAATGATAAAA | 2074 |
rs569577728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497325 | GCAGGGATTAGGAAA[C/T]AACCAATCAAAAGCT | 2074 |
rs569615395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504647 | AACAAAGAATCACTG[C/T]AGAGAAAACAAAAAG | 2074 |
rs569667217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510801 | ATGGTCAAATGGGGT[C/G]ATCCAGAAATGGGTT | 2074 |
rs569677046 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533689 | GCACCTATAGTCCCA[A/G]TTACTCAAGGGGCTG | 2074 |
rs569800283 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457367 | TATAATCCAAAAAAA[A/C]CTAGAAAATCCTGAC | 2074 |
rs569803631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518302 | GAAACAATGCTTGTC[C/T]GAGTCTGCTGCAGCA | 2074 |
rs569825637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490635 | TGGGATTACAGGCAT[A/G]AGCCACCACGCCCGG | 2074 |
rs569846055 | snp | C/T | 0.000545072 | 0.0164997 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524249 | CCATCTCCAGACAGG[C/T]CCGCCTCTGCCCCCT | 2074 |
rs569879100 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531237 | CAAAGTCTGGAAGCA[C/T]CCTAAATATGCTTAA | 2074 |
rs569969827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502419 | AAATTCCGAAAATAT[A/G]TGGTATGTAATCAGA | 2074 |
rs569995837 | in-del | -/TGTAAAGGT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499508 | GCACACTGACACTAC[-/TGTAAAGGT]TATCTCCAAATCATA | 2074 |
rs570001787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484506 | GCACTTTGGGAGGCT[G/T]AGGGAGGAGAATCGC | 2074 |
rs570001897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530287 | CTGACTTGCAATTTT[C/T]CAACTTTGTGATGGG | 2074 |
rs570058439 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455177 | AAAACTAAAAATCTA[C/T]AAAACACCTAGGAAT | 2074 |
rs570070279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491187 | CATTTCCAATGTGTC[A/G]TCACCACAAATAAGC | 2074 |
rs570081448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530662 | ATACTTCCTAAATTA[A/G]GTGCCCCTAAATGAT | 2074 |
rs570116131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477416 | AGTGGAAGATGGGGG[A/C]ATTCCTGAGAAAATT | 2074 |
rs570241965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526884 | ACAGATCTGTATAAG[A/G]TACTAGTAGAACCTA | 2074 |
rs570265681 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521660 | ATGAAAACCAGGGAA[C/T]CCACTGAGGAGTCAG | 2074 |
rs570278345 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478277 | CCAGACTCTCTCATC[C/T]GCAGAGGAGAATCAG | 2074 |
rs570287033 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474789 | ACGAATAGGAATGCA[C/T]GAATGGGAAAGATAT | 2074 |
rs570318531 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | ERCC6 | GRCh38.p7 | 10:49532712 | GGGCCTGGGCGCTAG[C/G]CTCTACTGCCTGGAT | 2074 |
rs570342939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487295 | CTATTAATAATTTGA[C/T]AGGTGTGTGCCATAC | 2074 |
rs570479069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488069 | AAGACAAATCATCTC[A/G]GGCGGTTTCAAATTA | 2074 |
rs570490623 | in-del | -/AAG | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479480 | GAATAATACATAAAA[-/AAG]AAGCTCAACTAATCA | 2074 |
rs570513850 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480688 | GGCCAACACCACCTT[A/G]AAGTAATCAGAGTTA | 2074 |
rs570517103 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520935 | CGTAACATTGTTAAT[A/T]TGGATAAGGGTCATA | 2074 |
rs570621936 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511399 | CTGCACCCAAATAAA[G/T]TAAGTGTGTTGTTCA | 2074 |
rs570639144 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455621 | ATTTTAAACTGGTGG[A/G]GAAAAGAATATTTGT | 2074 |
rs570658188 | in-del | -/TTC | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502697 | CTCAGCCAGGGGTAA[-/TTC]TTCTCCCTATGGGAC | 2074 |
rs570670706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515260 | CCAAAATTGGAACAC[C/T]AGGCAAAACCACTGC | 2074 |
rs570700505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467893 | TATTGGGTTCCAGAC[A/T]TTGTGAATTTCATCT | 2074 |
rs570709813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515925 | CGATAATCAAATGTG[A/C]CTCTTTCTTTTTTCT | 2074 |
rs570742772 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537451 | TCCTGTCCCCAAAGA[A/G]CTTAGAGTCTCATGG | 2074 |
rs570753448 | snp | A/G | 3.29484e-05 | 0.00405871 | missense | ERCC6 | GRCh38.p7 | 10:49532828 | CCCACAGAACGAAAG[A/G]AGAGGTACTCCTCCA | 2074 |
rs570789415 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462423 | TACAAGAAAACATGG[C/T]GAATTATCATATGAT | 2074 |
rs570822434 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455131 | TATGCTAATTCTCCA[C/T]ATTTTTATGTAAGTT | 2074 |
rs570875784 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458656 | AACTTTCAGAGAAGA[A/G]TTTCTTCTTCCTTAA | 2074 |
rs570932525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495052 | TGCATCTGCACTCCT[C/T]CTGCCCTTCTGGGAC | 2074 |
rs570945711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482118 | CAAGTGGGTCTCTTC[A/G]CTGCGCCCTGCCACA | 2074 |
rs570960304 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534048 | CTGAAGCAGGAGAAT[C/T]ACTTGAACCCAGGAG | 2074 |
rs570982870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488972 | TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACCAT | 2074 |
rs571058143 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519086 | TGAGCCATCTCCCTA[C/T]ATCCTCATCCAAATT | 2074 |
rs571099285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484725 | AGGCTAGACAACGGC[A/G]CAAGATCCTGACTCA | 2074 |
rs571121931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465145 | GGGCAGAGCTGCCCA[A/T]GACCATAGGAACCCA | 2074 |
rs571152289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522976 | AAAAGAATTGACACA[A/T]CTATTTCGGAAAGGT | 2074 |
rs571163484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485300 | GGTGGAGTCAGAATT[C/T]GAACGGAGAAAGGCA | 2074 |
rs571193512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529154 | CCCTTGGGCTTCACT[A/G]GGGAGGCCCAATGAA | 2074 |
rs571223855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464737 | CAGGCTGTGGCTTCA[G/T]ATGGTGCAAGCCCCA | 2074 |
rs571293329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498008 | TCAATTTATTTCCTT[C/T]TCATTATAAGATTGA | 2074 |
rs571313595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512720 | CCCAAGACTAAATAC[A/G]AATTCATTTATGTTT | 2074 |
rs571324134 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537498 | AAAACTATATATATA[C/T]ATATACACATACACA | 2074 |
rs571325074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479086 | ATGGAGCACGGCCAC[A/G]TGAGATGAGTACTAA | 2074 |
rs571326092 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529269 | AACATAAATGCCACA[C/T]TGCAATGACTTGCAA | 2074 |
rs571346258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492482 | CTCAACAGAGCTCAC[A/G]GTCTGGATGGTTAGA | 2074 |
rs571351074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507414 | CTAAGGAAATAGCTA[A/T]CATCTAACAACAGTT | 2074 |
rs571372686 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49482540 | AGATAATTTTGTGAT[-/T]TTTTTTTTTTTTTTT | 2074 |
rs571375494 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49505321 | AAACCTGGCTTCAAA[C/T]AGCAACTTAATCATC | 2074 |
rs571405345 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502616 | GAAAAAAATGAGCAA[C/G]CCAGAGCTGAAATCC | 2074 |
rs571502203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499140 | TTTCACATGCTTCCA[A/T]GCAAAATGTAATAGA | 2074 |
rs571528895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463300 | GACTGTGACCCATCA[C/T]ATGAAGTCAGGTGTG | 2074 |
rs571582885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500848 | TACATGAGTATTATA[G/T]TTATAAGGTCATACA | 2074 |
rs571601950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531465 | ATTTGCTGTTTGTAT[C/T]CTCTGTGGATTACAG | 2074 |
rs571618104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508078 | AACTATGAACGCAGA[A/G]CCAAACTTCTGCATA | 2074 |
rs571669209 | snp | A/G | 3.29582e-05 | 0.00405931 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515476 | TTATGCCATCATAAC[A/G]TGAGTCAATGTTACG | 2074 |
rs571672667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520061 | GTACATACAACTGTG[A/C]AGGGCACATAAAAGA | 2074 |
rs571736006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513245 | CTCACTCCATGGCCC[A/G]TGGTGTCTAACCCCT | 2074 |
rs571750345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465776 | TACTTGCTCCTCCTT[A/G]CATGATTGTAAAGCC | 2074 |
rs571830695 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496158 | TACCTTCTACTCAAC[A/G]TTCAGATCTCTAGCT | 2074 |
rs571834195 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468771 | AATACCATTCTCCAG[C/G]GTTCCTTGAAGAAAT | 2074 |
rs571848595 | in-del | -/AAG | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503367 | TGTGAGTGTGTTTAC[-/AAG]AAGATGAACAGCACT | 2074 |
rs571949821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538395 | TATGCCAGAGACCAC[C/T]TGGACAACTGTGCGG | 2074 |
rs571957636 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502953 | CTGCAAAAAGCTCTC[A/C]AAAAAAACTGATGTG | 2074 |
rs572030417 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502296 | TGCTTATTAAGTTTG[C/T]TAATTATAATACACA | 2074 |
rs572045802 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49530163 | TGACCCTAAGCCAGG[A/C]CAAAGAAATGGTGAT | 2074 |
rs572057854 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487445 | GAATACAGCAATAAA[C/T]GCCTTGGGGTGCACA | 2074 |
rs572079561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529222 | AGAATGTTTCAACTT[C/T]AAATACGAGTGTGGG | 2074 |
rs572119826 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522781 | TGTTCAAGAGTACTG[A/G]GCAACATTCCTCAAA | 2074 |
rs572221090 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469657 | CTCAAGGCCATCACA[C/T]TGTGAACACAGTGAC | 2074 |
rs572235186 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455793 | TGTTTGATTTTGTAC[A/G]TAATCAGGGAAATTC | 2074 |
rs572306651 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499969 | CAGGGATCAGACAAG[-/T]TAACTTCATTCAAAA | 2074 |
rs572314381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495142 | TGTATCTCCACAAGC[A/G]GCACTCCCATTACTG | 2074 |
rs572336441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489430 | AAAATTTACCCATTT[C/T]ATAAGTGATCAAATC | 2074 |
rs572342010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475469 | GAGATTCATGGAGAT[C/G]AATAGATGTGAATGA | 2074 |
rs572373000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488801 | TGCTTTTTTTCTTTT[C/T]GAGACAGAGTCTCGC | 2074 |
rs572405307 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469305 | TCAACTTGTAATAGG[A/C/T]CAAACCAGCATGTGT | 2074 |
rs572476594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531730 | AGAAAACATGTCTTT[G/T]AAGTACCAACAACCA | 2074 |
rs572507617 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517480 | TGAAAAATCAGACCT[G/T]GGCAATGACCTTGAG | 2074 |
rs572528922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475972 | CGCAGCTGCATTTGC[A/G]TCTGGGTTCAGATCC | 2074 |
rs572536447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523157 | GGGAAAAAGCCATCC[C/T]ACTATCAAGTATTTT | 2074 |
rs572761027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466700 | AGAATTTTATGCAAA[C/T]GGCATCAGAGTATGT | 2074 |
rs572761160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460293 | TGACCATTTTCTTCA[C/T]ATCCAGAATCAGGTG | 2074 |
rs572762322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504264 | TGAACAGAAGTTTTA[G/T]GACATAAAATATTTA | 2074 |
rs572766266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525151 | CTCCGAAGTTCTCAC[G/T]TCATTGCTAAAACCA | 2074 |
rs572788644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478605 | GTCAGTGGGAAATGA[C/T]TGCAAAATGGTTTGA | 2074 |
rs572801370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511651 | AGCTGGTCTCAGACT[A/G]CTGACCTCAAGTGAT | 2074 |
rs572805066 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479350 | GTTAAAAAATTAACT[G/T]GTTAAAAAATGTTCT | 2074 |
rs572827363 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535431 | AAGGTTAAAAAGTGA[A/G]CAACACAGTGAGAAA | 2074 |
rs572849358 | snp | A/G | 3.30404e-05 | 0.00406437 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472352 | GGGAACGCACAGCCA[A/G]GAGTGGCCACTGTGT | 2074 |
rs572868879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485389 | AAAGAAAAAGTTTAA[A/T]AAGAAGATTGTATGT | 2074 |
rs572884395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525708 | TGCACAAATCATTAA[C/G]TGTAGAACTCAGTGA | 2074 |
rs572893437 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479730 | GCGAGCATGCTGGTT[A/G]GAGGTGCTGGTCAAC | 2074 |
rs572905700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484879 | CACTAAAAATGTCCG[A/G]AGGCAAAGAGGAAAA | 2074 |
rs572924581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460901 | CTCTAAAAAAAGAAA[A/C]AAAAAAAGGAACTGC | 2074 |
rs572931038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519294 | CTACTTCACAGTAAA[A/C]CTGTGGGCAAGCCAA | 2074 |
rs572931193 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537830 | CGGGTTCAAGCGATT[C/T]TCCTGCCTTGGCCTC | 2074 |
rs572967523 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486760 | CTCTTCTCACCAAAA[A/G]TCTACCAGACCCAAA | 2074 |
rs573031406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513335 | ATTACATATACACAC[A/C]TACATACATATTTCT | 2074 |
rs573054350 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485443 | ATCATTAAAGCATAA[A/C]AACAAAGCCTAAATA | 2074 |
rs573120489 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540693 | GCTGGAGTCCTAACC[C/G]CCACTCCCCACCCCC | 2074 |
rs573135787 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481359 | AAAAAAGAATGGTAT[-/A]ACAGGAGATTCAGAG | 2074 |
rs573179964 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513786 | ATATGGGGACTACAA[-/T]TCAAGATGAGATTTG | 2074 |
rs573195636 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513921 | CAAGATTACCAATGA[C/G]TTAAGGGAAAAGATT | 2074 |
rs573200363 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514912 | GTCTATCTGGGTAAA[C/T]TTAATTGGCAAATCT | 2074 |
rs573202726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500330 | TCAATGCCTGGAATT[A/C]ATTAAAAGTGTTACA | 2074 |
rs573216672 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479434 | TGTTGTATGAATGCA[C/T]GTGCGTAAATATTAA | 2074 |
rs573246939 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509337 | CAGATACTATTACTA[C/T]GTTCACTGAAAGAAG | 2074 |
rs573253582 | snp | C/T | | | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514613 | GTAAGGAAAAAGCTG[C/T]GTATCATACAGTTAA | 2074 |
rs573285974 | snp | C/T | | | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514891 | TTTCTTATCTTCCTT[C/T]TTATGGTCTATCTGG | 2074 |
rs573370438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490244 | AACAAAGATAACATA[C/G]GATCAAAGGGTGAGA | 2074 |
rs573412376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473952 | GAATCATTACTTTAG[A/G]TTGAATCCCATTTTG | 2074 |
rs573493890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521227 | ATCAATAACATGGAG[A/G]TAACAAGGACTGGGG | 2074 |
rs573649842 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526401 | TTTTGTGTAGGAAGT[A/G]TTCCAGTCTTTCGCC | 2074 |
rs573655290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511836 | AGAGAAGTGAAAACC[A/G]AATGTAGGCAAAAGA | 2074 |
rs573686469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495983 | CTGGACGTGGCCTAC[A/G]AGGCCACGAAGACTG | 2074 |
rs573753768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529938 | AAATATTCCCTACCC[C/T]TAAGTTTTCCAAAGC | 2074 |
rs573799225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482942 | TAAAACGCTCCTCTG[C/T]AAATTATTTACACAT | 2074 |
rs573826684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534874 | CAGCAATAAAGCACC[A/G]GGATACAAAGAATTC | 2074 |
rs573850458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476890 | ATGCTCATTTAGCCA[C/T]CCCTCTGCCACCTAC | 2074 |
rs573890928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535804 | GAGTGAATTTGGATA[A/C]CAATGGGTCACCATT | 2074 |
rs573915835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523837 | AAGACCTAGAAGTAC[A/C]TGCATTTGGGGCCAG | 2074 |
rs573984754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477566 | CCAAACACACTGGGT[C/T]CTTTCCAGGTCACCC | 2074 |
rs574011598 | snp | C/T | 4.94311e-05 | 0.00497123 | missense | ERCC6 | GRCh38.p7 | 10:49470737 | CTTCAGCTCCTTTAG[C/T]CTCAGATTTCTCTTC | 2074 |
rs574041201 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537236 | GTAATCCCAGCTACT[C/G]GAGAGGCTGGGGCAG | 2074 |
rs574043055 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457895 | AACAAGAAAGCCCGT[C/T]GCAAGGAATGCAAAG | 2074 |
rs574053311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514121 | CTAAAACTTCAATCC[A/G]AATGTTGTCTTAAAA | 2074 |
rs574061320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521093 | AAGTCTATTAACAGA[C/T]TGCAAATTTTTTGCC | 2074 |
rs574064255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505015 | TGACAGCTGAATCTA[C/T]AAAGGAGACCAAACT | 2074 |
rs574092445 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527315 | TATCAATGAGAAACA[C/T]AGTACACAGCAGTTA | 2074 |
rs574101642 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467033 | TGATTCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 2074 |
rs574142370 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464834 | AACTTCTGCCTAGAT[A/T]TCAAAAGATGTATGG | 2074 |
rs574163356 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537625 | TTGTGGAGGTAGATG[C/T]GGGGTCAAGGAGGCC | 2074 |
rs574196051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505809 | CCACAGGTAACTACT[A/G]TGTAATTCCTAAAAT | 2074 |
rs574227807 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492296 | CTGGGCCCCGAGAAC[A/G]AACTCAAGAGCTCAG | 2074 |
rs574272317 | snp | C/T | 0.00041389 | 0.0143796 | missense | ERCC6 | GRCh38.p7 | 10:49459231 | CCTTTTTCATGATGC[C/T]ATCCTATAAAAAGAA | 2074 |
rs574277533 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539167 | GCACGGGCAAGACCA[A/C]GTGGTTTGGAGGGAC | 2074 |
rs574294118 | in-del | -/CT | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509403 | GCATATTGCAACGTA[-/CT]CTGTTTAACAGAACT | 2074 |
rs574307052 | snp | A/C | 1.64814e-05 | 0.00287061 | missense | ERCC6 | GRCh38.p7 | 10:49458852 | TTCCAAATTCCTTCA[A/C]CACCAGAAGTTCTAT | 2074 |
rs574356162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492269 | ATAGCCCTTGCAGCC[A/G]GCACTGCTTTCCTGG | 2074 |
rs574392001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491636 | TCCATAATGAGTCCA[C/T]GTATGTGGTTTACAC | 2074 |
rs574411264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480724 | ACCCATAGTGGAACA[A/G]ACAGACAGCATGTTC | 2074 |
rs574466336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534116 | TCCAGCATAGGCAAC[A/G]GAGTGAGACTCAATC | 2074 |
rs574504271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501603 | AACACTTAACAACAG[A/G]GAATGGTATGAAGAT | 2074 |
rs574517515 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473200 | TCACAGCTTTTACTT[C/T]TAATATTTAATAGAA | 2074 |
rs574542172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467411 | CTTTCATTTTAGCCA[C/T]TCTAGAGGGTGTATA | 2074 |
rs574659871 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497960 | ATTACCAAATGATAT[A/C]CAAGACTTTAAAAAA | 2074 |
rs574722582 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455132 | ATGCTAATTCTCCAT[A/G]TTTTTATGTAAGTTA | 2074 |
rs574747795 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469950 | GCACACCTCCCATGA[G/T]TGGCCATAAGTACTA | 2074 |
rs574750716 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533571 | GAGGATAGAGACCAG[C/T]CAGGGAAACACAGCG | 2074 |
rs574754418 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462853 | GGGCAACAACTGCTC[A/C/G]TGACAATTCAAATTG | 2074 |
rs574804740 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493921 | GCCCACACCGACAGT[C/G]TACAAGCTGGCACTG | 2074 |
rs574807711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474873 | ACAAAAGAACATTAA[C/G]AAAACTTCAATAATG | 2074 |
rs574848184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482292 | TTCTCCACTACTTTA[C/T]AAGATGCACTACCCC | 2074 |
rs574874727 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522478 | TCTGAAATTCATTTG[A/G]GATTTCACTGTAGCT | 2074 |
rs574930725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488696 | CTTTTTTTAAAGCCA[C/T]GTCTTTTTGCTCTAG | 2074 |
rs575009184 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475428 | TCTAGACCCCCTAAC[G/T]TGGAAAGACCTGAAG | 2074 |
rs575014600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503139 | TCCAACAACTCTTTT[G/T]GCTTGGGGCTCATCA | 2074 |
rs575022267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522037 | AGGCTATACCCTCAG[C/T]AAAAGGTGTTAAGTT | 2074 |
rs575094358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472243 | AGAAAAAATACAAAA[C/T]AAAAACCAAAGCCTT | 2074 |
rs575153385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465381 | GATTTTACAGGCTCA[C/T]AGGCAGAAGAGACTT | 2074 |
rs575154829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530449 | TTACGATGGGTTTGT[C/T]GGGATGTAACCCTGT | 2074 |
rs575155109 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499528 | AGGTTATCTCCAAAT[C/T]ATATATAGGGAGTGT | 2074 |
rs575155661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472662 | CTCTACTTGAAAAAA[C/T]GTTTGTAACTTTGCC | 2074 |
rs575170076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510880 | TTCCTACTCCTTCTA[C/T]CCATATGACTTTAAA | 2074 |
rs575210023 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536423 | TCGCAAGCAGAAATG[A/G]ACAGGAGGCACAACA | 2074 |
rs575214077 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457353 | AGAAATGAACAAGCT[A/G]TAATCCAAAAAAAAC | 2074 |
rs575257561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465925 | ATGCCAGAAACTCAT[A/G]AGACTGGTAAGGTAA | 2074 |
rs575270436 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49482286 | CTAAGTTTCTCCACT[A/G]CTTTATAAGATGCAC | 2074 |
rs575284244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531025 | CATTAGAGGTTTAAG[A/G]TGACTGCTAGTGTTT | 2074 |
rs575308702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484337 | AATCACCATAAATGG[A/T]GCCGAGATTTGAATC | 2074 |
rs575317982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492672 | AAAGCAACAATACTT[A/G]CGAAATTCTCAAGAT | 2074 |
rs575357449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491499 | TGTATGCAAGTGTCT[A/G]TGAAGGTAAAACAAC | 2074 |
rs575385106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478570 | AAAAAAAAAAAAAGA[A/G]TAACCAACAGCTGTA | 2074 |
rs575392357 | in-del | -/AC | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460672 | ATGCCTGTAATCCCA[-/AC]ACTTTGGGAGGCTGA | 2074 |
rs575442315 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513305 | CAGCTAGCTCTGGAC[A/G]AGTTTTGTTTTGAGA | 2074 |
rs575455198 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462793 | TTCTCACCTATCAGA[C/T]TGGGAAAAATTAAAA | 2074 |
rs575477841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519246 | GGAAGGAAACATGTA[C/T]GTAGAGGGCCCAGCC | 2074 |
rs575489032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506137 | TAGGTTAATGCTGCC[A/G]TTATTACCCAAAACA | 2074 |
rs575502693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507155 | CAGAGCCCAATGCTA[G/T]TATGTAGGTAGCTAC | 2074 |
rs575523907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512973 | GTCACCTTTTCATAC[A/G]TATGAGTATTCATTA | 2074 |
rs575533299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460242 | ATCGTAAATCAGAGC[A/G]TGCAACACAAATATC | 2074 |
rs575641131 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456165 | CTTAAGCAAGTCAGT[A/G]TTTTATTTTACTCTT | 2074 |
rs575705047 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491738 | ACACACACTTTACTA[A/C]CCCAAAAGAAAATGA | 2074 |
rs575709699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495276 | ACTCAGCTCATGCTA[C/T]AAGAGGCAACTAAAA | 2074 |
rs575722996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532412 | TGAGGACTGCCCTTA[C/T]TGACTCTGTCCTCCA | 2074 |
rs575747313 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503030 | TGCTGAGATACAGAA[A/C]AACTGGACCAGCTCC | 2074 |
rs575818370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480221 | AGTCATCCCTTCTCC[A/G]AGAAGCCTTTCTGAG | 2074 |
rs575841255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485700 | TGCCAAAACTTTATG[C/T]TGATTACTGAGTAAC | 2074 |
rs575846658 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519525 | CAACTCAAATCCACT[C/T]CAGGCTATGCATTTA | 2074 |
rs575856979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486649 | CTGAACATTTTGACA[C/G]ATATGATAGCTAAAA | 2074 |
rs575858508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537944 | TAAGGCTGGTCTCGA[A/C]CTCCTGACCTCGGGT | 2074 |
rs575883570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526491 | GTCCTTTGATTCACA[C/T]ATGTATTGCAAATAT | 2074 |
rs575920705 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538523 | CTGCGTGGAAGTCAC[A/C/G]TAACAGCAGCATTTA | 2074 |
rs575928193 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540593 | ATTATTTACAAAGAC[A/G]TGGGCGGGGTTCAGG | 2074 |
rs575938223 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489882 | TCCCCAAGGAAAGAG[A/T]TGGCTTTTTAAGGTT | 2074 |
rs575942684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510277 | GTTAATTTATTTTAG[A/T]AGAATTTTCAGCATT | 2074 |
rs575964618 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462239 | TGGAAATGTACTACA[A/T]GATAAAGGCATCTCT | 2074 |
rs575970992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462773 | ATTAAAACTTAAGAT[A/G]TCCTTTCTCACCTAT | 2074 |
rs576028491 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523203 | CCTTTTTCCCTTTGA[A/C]TTCCTTAGAGCTAAG | 2074 |
rs576114745 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529769 | CAAGTTGGGATGGCA[A/G]AACTGAAATGGTTAC | 2074 |
rs576136412 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489230 | TTCTCTCTAGACTAC[A/T]TACTGAGTCAATCAG | 2074 |
rs576163821 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534742 | AAACGATAACCAAAA[A/T]TCAGTCTTGCTTTTT | 2074 |
rs576171137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534250 | TCCAATACAGACAAG[A/G]AGAAGGATCCCCCCT | 2074 |
rs576284241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528334 | CTCAAAACCCAGGCA[A/G]AGACTAAAGAGACAC | 2074 |
rs576297930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490161 | AAACTATCAGTTGTA[C/T]ATTTTTTTGCATGGC | 2074 |
rs576318272 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469393 | AAAAAAATGTATGCA[C/T]AGATGGGTGTGTGTG | 2074 |
rs576322834 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529271 | CATAAATGCCACACT[G/T]CAATGACTTGCAATT | 2074 |
rs576360518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529902 | AGTTTCAAACTTCAT[A/G]AAAATAATATCCTAA | 2074 |
rs576468810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495141 | TTGTATCTCCACAAG[C/T]GGCACTCCCATTACT | 2074 |
rs576474689 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511770 | GTCTCAGGCTCCAGT[C/G]GTGGTCACTAGAAGA | 2074 |
rs576509154 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497144 | AGTTTCTAAGCCATG[C/T]TCCTCACCAAGGCAG | 2074 |
rs576511403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512378 | ACCTACACTTAGAAC[C/T]AAGGGGCATGTTGCA | 2074 |
rs576528024 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467436 | TGTATAGTGGTATCT[C/T]GTTATGGTTCTAATT | 2074 |
rs576562742 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457835 | CCACAAACACATAAA[C/T]AGTAGTGAGATACAA | 2074 |
rs576565789 | snp | A/G | 0.000345967 | 0.0131478 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470666 | GCTAGTTACATTACT[A/G]CTCATGTGAGGGTCA | 2074 |
rs576597680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464343 | TCTAAGCAGCAAAGC[A/G]TTCAACAGGTGACAT | 2074 |
rs576744368 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500997 | ATAGCTTGCTAAACA[A/G]GCATAAACTTACTAT | 2074 |
rs576786822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497564 | ATTTTCCCCCTTAGT[A/G]GAAAAAATTGGAGAT | 2074 |
rs576799522 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486588 | AGGAACACAATTACA[C/G]ATGTAGAGAATACAA | 2074 |
rs576895536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480153 | AGCAGCAGTCTATAT[C/T]TGGGCTGCTGACATG | 2074 |
rs576897572 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472810 | AAAATGTGAAACGTA[A/T]GCTGAAGCCAACCAG | 2074 |
rs576931213 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479343 | AAAAAAAGTTAAAAA[A/G]TTAACTTGTTAAAAA | 2074 |
rs576949155 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467346 | CCCACCAGGCGTGTA[C/T]GAGACCCAACTGCTT | 2074 |
rs576964243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473103 | CTCTGCCTCCACATA[C/T]TGTACACATGGAATT | 2074 |
rs576981832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466733 | TAATCTTACTAGTCC[A/G]AAAGTCATCCATGCT | 2074 |
rs577021605 | snp | A/G | | | stop-gained | ERCC6 | GRCh38.p7 | 10:49532904 | TATTACTGACAGGTT[A/G]ACTCTGTAAACAGTC | 2074 |
rs577050209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481814 | TTCTGCCTAAAAATG[A/C]CACCTGCGTCTCCTG | 2074 |
rs577063024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507819 | AGGACAGCCCCCAAA[C/T]CCCTCGGTAAAAAGT | 2074 |
rs577100883 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538624 | CATCTAGCCCGACTC[C/T]CTTTAAAATAACAGC | 2074 |
rs577145652 | snp | A/G/T | 3.29692e-05 | 0.00406001 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532947 | TTGACTTGAGTGGGG[A/G/T]ATTCCCTCATTTGGC | 2074 |
rs577148279 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539547 | CGCACCTGGGCGGAG[C/T]GAGTGCCTACAGAGC | 2074 |
rs577159169 | snp | C/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540504 | GGTTCCCTTTGCAGC[C/T]ATTTTGGAGACCCTT | 2074 |
rs577167742 | snp | C/T | | | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516482 | GGCAGCACTAACCAG[C/T]ACATTATGCACATCT | 2074 |
rs577168011 | in-del | -/AAC | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499202 | ATATAACTTCCTTGT[-/AAC]AACAACAACACGATG | 2074 |
rs577184007 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49539077 | ACCATAGACACCGCC[C/T]CCAACAGCGACTCCG | 2074 |
rs577185241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501528 | TGATATGTTTAATCT[A/G]TAACCTAAAAATAAA | 2074 |
rs577223895 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508425 | CTAAAATATACAGGC[A/G]TCTTGTCGCCACAGA | 2074 |
rs577268340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494371 | TAAGATGGAATATCA[C/T]ATAACTATTAAAATC | 2074 |
rs577278202 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487681 | TTACCAAATGAGACA[A/C/T]CAAGCTTCCCAAATG | 2074 |
rs577303652 | snp | C/T | 0.00013182 | 0.00811742 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516715 | TTACGGTGAAGAAAT[C/T]GTTTGGTGGTGCTGT | 2074 |
rs577381204 | snp | C/G | | | missense | ERCC6 | GRCh38.p7 | 10:49482803 | CAAAGAGCGACCACA[C/G]CTCTCGGAGGTTATT | 2074 |
rs577441135 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477059 | CCTGTCCTGCTCCAG[A/G/T]GGGTCCTCTACGCAT | 2074 |
rs577452362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527210 | AGCTATTAACCCTAA[A/G]AGGTAGCTATTAACC | 2074 |
rs577455788 | snp | C/T | 8.28452e-05 | 0.00643551 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516279 | TGTTTGCACCCGTGA[C/T]GACCAAAATAAGGAA | 2074 |
rs577456876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509268 | CTTAATAAACTACTA[C/T]AGTATTATATAAAAC | 2074 |
rs577518491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527909 | AGTTCCAGAGCTTAC[A/G]AATTTTCCCAAAAAG | 2074 |
rs577566863 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505452 | ACAATATAAGACACT[A/C]AAAAAAAATGTCAAA | 2074 |
rs577614996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496932 | TTGTAGTTCTATAGA[A/G]AAACAATGAAATTTT | 2074 |
rs577630302 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491418 | TTCCTCAAAAGTTAA[C/T]TAAGAATCTTCAAGT | 2074 |
rs577642058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522370 | TAACAAATATTTCAA[C/T]GTGGATATCTGCAGT | 2074 |
rs577658979 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475053 | GAATAAGTCAGGAAC[A/C]TTGGTAAACCTCCCC | 2074 |
rs577675179 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497511 | TCTTCTGGCTGAACA[A/T]CTATCTGGCATTATC | 2074 |
rs577702875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507089 | GTAATACTACACATG[C/T]TGCCTGGCCAAAGGT | 2074 |
rs577706147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536360 | CTGGAGGGAGACAGA[A/G]GAGATAACCCAGAAA | 2074 |
rs577716477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484902 | GAGGAAAATCTTTAC[A/G]TAATTCTAAGAAGGA | 2074 |
rs577738925 | snp | G/T | 1.66161e-05 | 0.00288232 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506064 | GATCACAAGACAGAT[G/T]TAAAAAGATAGCTCC | 2074 |
rs577796698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531206 | TGGGTTTTTTAAGCC[C/T]GTTACGGAAGCCTTC | 2074 |
rs577853718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530021 | GAAGGGCCAAGCTCT[C/T]GCAACTGTCAGCAAA | 2074 |
rs577856375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519163 | AGGTGGGGGCAGCTA[C/T]GTGTTGATTTTTGGC | 2074 |
rs577897299 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518551 | ATCATTGTTCTTGTG[C/T]ACCACTCCCGCCCCT | 2074 |
rs577909433 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490197 | GGTGTACATTTGACA[A/T]TTCTAAATTATGCTG | 2074 |
rs577916827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530437 | AATATTTTCAATTTA[C/T]GATGGGTTTGTCGGG | 2074 |
rs577919468 | snp | A/G | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512869 | CACTTGTGGCATCAC[A/G]TTGCTAAAAAATTTT | 2074 |
rs578024401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525049 | TGCCATCCAAAGATA[C/G]GCTTATTACTGTATA | 2074 |
rs578081705 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491906 | AGGGTAGTGACAGGA[C/T]AGTTTAAGGTTTGAC | 2074 |
rs578094376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537869 | CTGGGATTACAGGCA[C/T]ATGCCATCATGCCCG | 2074 |
rs578136460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537283 | CAGGAGGCGGAGGCC[A/G]CAGTGAGCGAGATCG | 2074 |
rs578151883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492319 | GAGCTCAGAAGACTC[A/G]GGAAAGAAAGAACTA | 2074 |
rs578157056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520357 | CTCACTGTAGTCTGC[A/G]AGGGCAGCAACTTAA | 2074 |
rs578160397 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485452 | GCATAACAACAAAGC[C/T]TAAATATTAAACACT | 2074 |
rs578171795 | snp | A/C | 0.00019988 | 0.009995 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459257 | AAGAAGACCACTATA[A/C]TGATATATTTAATTT | 2074 |
rs578216451 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463329 | TGGAATTTTCCACAT[C/T]TGGCATCATGTCAGT | 2074 |
rs745313254 | snp | A/G | 0.000115349 | 0.00759349 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515563 | AATGGCATACCACAC[A/G]TCGACGAAACTCCAG | 2074 |
rs745327263 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504541 | TTACTACAAATACAC[A/G]GAAGTATCCTGTCTT | 2074 |
rs745333287 | snp | C/T | 3.2987e-05 | 0.00406108 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483526 | TTTCTCCTGAGACCA[C/T]AATAAAATGGTAAAG | 2074 |
rs745341304 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470645 | CTCTTCTCCAAGCCT[A/G]TCATTGCTAGTTACA | 2074 |
rs745344281 | in-del | -/AAG | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481258 | TCTGGGTGAAGTGTT[-/AAG]AAGGTTTTCTTGTTT | 2074 |
rs745352643 | snp | C/T | 3.29516e-05 | 0.00405891 | ERCC6 | 10 | allele_origin=T(germline)/C(germline) | 10:49459111 | GAATCAGGTGGTTTC[C/T]AGCTCTCATTTTAGC | 2074 |
rs745401370 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460603 | TGCTCTATCCCCCTC[A/G]ATTCTTCCACTCCAC | 2074 |
rs745402291 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503300 | GGCAGCATACAATGT[A/G]CTGGGTGTTTCCTCA | 2074 |
rs745425336 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473263 | ACATGCTGTAGAAAA[C/T]GCATTCTTTGTTTGA | 2074 |
rs745487504 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516704 | GGGAGTTCTCATTAC[A/G]GTGAAGAAATCGTTT | 2074 |
rs745500415 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515475 | TTTATGCCATCATAA[C/T]GTGAGTCAATGTTAC | 2074 |
rs745512267 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484336 | CAATCACCATAAATG[G/T]AGCCGAGATTTGAAT | 2074 |
rs745524303 | in-del | -/CCT | 1.64795e-05 | 0.00287045 | cds-indel, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524093 | CTTCCCACTTTCCGA[-/CCT]CCTCCTCCTCCTTCT | 2074 |
rs745530799 | snp | A/G | 6.75493e-05 | 0.0058112 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472915 | AAAACAAACCTGCGT[A/G]TCCGTGCTTGGGTTC | 2074 |
rs745542318 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526480 | CCTAGATTTGAGTCC[-/T]TTGATTCACACATGT | 2074 |
rs745575045 | snp | A/T | 3.29761e-05 | 0.00406041 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516622 | CTTTACTGCAAGCAT[A/T]TAAGTTGGAGTACTT | 2074 |
rs745601071 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511988 | AAATGAAATTATGTA[G/T]GTACATTATACTTTT | 2074 |
rs745608661 | snp | C/G | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525045 | TCTCTGCCATCCAAA[C/G]ATAGGCTTATTACTG | 2074 |
rs745622301 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480106 | TCTTCTCAGTTCTCA[C/T]ATGCCCTGCCCCAGC | 2074 |
rs745639461 | snp | A/C | 1.66574e-05 | 0.0028859 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516171 | GTATTTGGGTTTTTA[A/C]CCTGATACGGCTGAA | 2074 |
rs745652875 | in-del | -/T | 1.64817e-05 | 0.00287064 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49470803 | AGGGAACTTCTTGCG[-/T]TTTTGGAACATCATG | 2074 |
rs745709338 | snp | A/G | 3.29679e-05 | 0.00405991 | missense | ERCC6 | GRCh38.p7 | 10:49471065 | TGGATTTGAAAAACC[A/G]CCTTTGTTTTGGGTC | 2074 |
rs745713027 | snp | A/C | 1.6793e-05 | 0.00289763 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476190 | GTCCACAATTCATTT[A/C]TCCAGCTTCTATTTT | 2074 |
rs745758957 | snp | C/T | 1.64944e-05 | 0.00287175 | missense | ERCC6 | GRCh38.p7 | 10:49459201 | TAAAATGCTCAGGGA[C/T]ATTATCTTTTCCCTC | 2074 |
rs745774078 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49493456 | AATCTCATTCATCAA[A/T]TAGTGGATGTAGGTG | 2074 |
rs745785349 | snp | C/T | 3.35065e-05 | 0.00409293 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474271 | GAGTACATGTACACT[C/T]AGATGACCCCATGTA | 2074 |
rs745785829 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478767 | TACACTTTCCTTTAA[C/T]TATTACTATACAGTT | 2074 |
rs745811481 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479539 | TAAATATATCATTCA[A/G]ACTGATGAATATCAC | 2074 |
rs745823725 | snp | A/G | | | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461552 | CATGACACTGTGCAC[A/G]CCAACTAGCAAGAAA | 2074 |
rs745864793 | snp | C/T | 1.65457e-05 | 0.00287621 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532512 | CATGTTTTACCACCA[C/T]TTTGAAAGGAAGAAG | 2074 |
rs745881925 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531493 | CAGGATAAACAATGC[A/G]TATTACTGGCTGAGA | 2074 |
rs745883689 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519045 | TGTCCCCATCCACAC[C/T]ATACTTGCCAGGTCT | 2074 |
rs745888254 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488308 | CGGCGGGGAGAGGAG[C/T]GAAGCACAGGCACAT | 2074 |
rs745894239 | snp | A/C | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515786 | CTGAACTTGTATCTT[A/C]TTTTTCAGTTTCTGG | 2074 |
rs745909036 | in-del | -/CTTTT | | | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514874 | ATACTTGGTGTTTTA[-/CTTTT]CTTATCTTCCTTTTT | 2074 |
rs745917661 | snp | C/T | 0.000116128 | 0.00761908 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49517088 | TAAAAGGTCAGTTAT[C/T]TCATGTAAACTTAGT | 2074 |
rs745984774 | snp | C/T | 3.30704e-05 | 0.00406622 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474005 | AACCAGCCTGTTTCC[C/T]GTCTGAAGTCTGTGC | 2074 |
rs746028344 | snp | A/G | 3.29707e-05 | 0.00406008 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49458833 | GCAGTATTCTGGCTT[A/G]AGTTTCCAAATTCCT | 2074 |
rs746051443 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516963 | GAACCTGGCAGATTA[C/T]TTATTGTTCCACCTT | 2074 |
rs746061767 | snp | A/G | 3.39968e-05 | 0.00412277 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482914 | TACCTTTTAGCAATC[A/G]CCATTCCTACCCTAA | 2074 |
rs746070758 | snp | G/T | 1.79355e-05 | 0.00299456 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528574 | AATGAAGTGATTTAT[G/T]GTTAAATACAAAAGA | 2074 |
rs746074690 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49473564 | CTTTTGGGCTCTAAG[A/G]AATACTTCAAGTATG | 2074 |
rs746081896 | snp | A/G | 1.78634e-05 | 0.00298854 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515323 | TTATCTCAGGAGGTG[A/G]TGACACCTGCTATTC | 2074 |
rs746104327 | snp | C/T | 1.64844e-05 | 0.00287087 | missense | ERCC6 | GRCh38.p7 | 10:49482845 | AGCCAGACAGAATGA[C/T]CCGATGAGGGGTGCG | 2074 |
rs746104875 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467597 | TTGACATGGGGTCTC[A/G]CTCTGCTGCCCAGGC | 2074 |
rs746111661 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489363 | CCTATTAGGGACCAC[A/G]CTAAGCTCTTCATAC | 2074 |
rs746121111 | snp | A/C | 1.64741e-05 | 0.00286998 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470300 | CAGGTGTGGAATTCG[A/C]GTTCCTTCAAACTTG | 2074 |
rs746146174 | snp | A/G | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49541115 | GAAGCTCTCCTCATG[A/G]CTTGCAAATGGTTAC | 2074 |
rs746159424 | snp | C/T | 1.64789e-05 | 0.0028704 | missense | ERCC6 | GRCh38.p7 | 10:49528450 | TGGCGTGATCTAGTT[C/T]AATTTTCACCTCTGC | 2074 |
rs746162012 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509238 | ACCTTAGCACAGAAC[C/T]TAGATTAGGAAGTGC | 2074 |
rs746184344 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49466627 | CTTTGTAATCCCACC[A/G]TCAAATACCCCATGC | 2074 |
rs746198255 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497298 | AAAAGAGTTATCATC[A/G]ATATGCACTTAGCAG | 2074 |
rs746231544 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538559 | GGCCTGCCTCATCCG[C/T]CCACACTCTTATCAA | 2074 |
rs746243560 | snp | C/T | 6.58924e-05 | 0.0057395 | missense | ERCC6 | GRCh38.p7 | 10:49532817 | ACAGCCCGTCACCCA[C/T]AGAACGAAAGGAGAG | 2074 |
rs746250916 | snp | A/T | 9.88696e-05 | 0.00703029 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524500 | GTTTGGTTTGTTTTT[A/T]TTTTGCACTGGGGCT | 2074 |
rs746280615 | snp | A/T | 1.65132e-05 | 0.00287339 | missense | ERCC6 | GRCh38.p7 | 10:49500664 | TGCTGGCAGTGCAAT[A/T]CCCACAGCCACCTAA | 2074 |
rs746299606 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469028 | ATCTAAAAATAAATT[A/G]ATAAATAAATAAGAG | 2074 |
rs746304128 | snp | C/T | 1.65233e-05 | 0.00287426 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470944 | ATCTTGTGCAATTGA[C/T]TACTTTAAATTAAAT | 2074 |
rs746330518 | snp | C/G | 0.000132199 | 0.00812907 | missense | ERCC6 | GRCh38.p7 | 10:49461373 | CCTGCTGGTGCACCA[C/G]AAATCCCCCTGTGGC | 2074 |
rs746372685 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49500561 | TGAACCACGAGTCCT[A/G]ATCTTGCTGTAGCTC | 2074 |
rs746377176 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476004 | CAGCACACAGCTCTG[C/T]AACTTTCCACCTTTC | 2074 |
rs746391541 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489426 | TACCAAAATTTACCC[A/G]TTTTATAAGTGATCA | 2074 |
rs746395860 | snp | C/T | 3.29669e-05 | 0.00405984 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515865 | GCAACAGTGACAACA[C/T]TGTTATCATTCCATC | 2074 |
rs746405584 | snp | C/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539841 | AGGCAGGACGTCCTC[C/T]GGGAGGGCAGTGACT | 2074 |
rs746408785 | snp | A/G | 1.65157e-05 | 0.0028736 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470858 | CCTTCTTTTTAGATG[A/G]CATTTGGGTGTCTGA | 2074 |
rs746424521 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | ERCC6 | GRCh38.p7 | 10:49532729 | TCTACTGCCTGGATC[C/T]GATGTCGGTCGATGT | 2074 |
rs746466273 | snp | A/G | 1.66294e-05 | 0.00288347 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460357 | CCCTGGAAAGCAAAA[A/G]GGTTATCTATATTAC | 2074 |
rs746481213 | snp | A/G | 3.29571e-05 | 0.00405924 | missense | ERCC6 | GRCh38.p7 | 10:49470622 | TCTGGTCCAGATACT[A/G]CATTTGTCTCTTCTC | 2074 |
rs746485418 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476032 | TCACCAGTTACCTAC[-/T]TCCTCTGCACCTTAC | 2074 |
rs746555352 | snp | C/T | 1.65091e-05 | 0.00287303 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532538 | AGAAGATGGGCTGCA[C/T]TCACGTGAGGTCATC | 2074 |
rs746568207 | snp | C/G | 1.64972e-05 | 0.00287199 | missense | ERCC6 | GRCh38.p7 | 10:49493160 | TGTAGAATTGCCACT[C/G]TGAACGGAGGCCACC | 2074 |
rs746572889 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478710 | ATTAACCAAAATGTA[C/T]AACAAAAGAAAAACT | 2074 |
rs746586048 | snp | G/T | 1.64963e-05 | 0.00287192 | missense | ERCC6 | GRCh38.p7 | 10:49459203 | AAATGCTCAGGGACA[G/T]TATCTTTTCCCTCCT | 2074 |
rs746616255 | in-del | -/TC | 1.65127e-05 | 0.00287334 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49505978 | CCAGCTTCAGACGTT[-/TC]TCTTTGTCCTGCAGT | 2074 |
rs746655921 | snp | A/C | 2.66628e-05 | 0.00365112 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488227 | TGGAGGCTCAAGAGA[A/C]CAATCCCTCCTAGAG | 2074 |
rs746657961 | snp | A/C/T | 6.5906e-05 | 0.00574016 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515682 | TACCATTTCTTTCCA[A/C/T]GGATTGATGCCCGAT | 2074 |
rs746661187 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481561 | TCAGCCATGACCTGG[A/T]AGGCACAGGCCCACC | 2074 |
rs746668742 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520617 | GGCTGGCAAATACCT[A/G]GCATGAATGTTGCTA | 2074 |
rs746671193 | in-del | -/A | 0.0139671 | 0.0823921 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476345 | GGAAACTATAATTTC[-/A]AAAAAAAAATTAACA | 2074 |
rs746676471 | snp | C/T | 6.59098e-05 | 0.00574026 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515568 | CATACCACACGTCGA[C/T]GAAACTCCAGAAAAT | 2074 |
rs746707577 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496219 | CTGTAAACAAGTTAA[C/T]GACTCTTCCTTAGTG | 2074 |
rs746764132 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460719 | TGAGGTCAGGAGGTC[A/G]AGACTAGCCTGGCCA | 2074 |
rs746772551 | in-del | -/A/AA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534133 | GTGAGACTCAATCTC[-/A/AA]AAAAAAAAAAAAAAA | 2074 |
rs746803430 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534235 | AGCCTGATAGATAAA[C/T]CCAATACAGACAAGG | 2074 |
rs746861269 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | ERCC6 | GRCh38.p7 | 10:49470232 | TCATTGCTCTGTTCC[C/T]TGGCCTCACTCTTGT | 2074 |
rs746867691 | snp | A/G | 1.64871e-05 | 0.00287111 | missense | ERCC6 | GRCh38.p7 | 10:49472424 | GTCAGGAGCCTGTAC[A/G]CAGTCACTTGCTTCT | 2074 |
rs746873591 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500382 | CAGCTCCATTGTCTC[A/G]TAAAATTTTTCCTTT | 2074 |
rs746946883 | snp | A/T | 1.66263e-05 | 0.00288321 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476204 | TCTCCAGCTTCTATT[A/T]TTTAGCTGACCTGCA | 2074 |
rs746998291 | snp | C/G/T | 0.000216407 | 0.0104 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516179 | GTTTTTACCCTGATA[C/G/T]GGCTGAAACCAGCAA | 2074 |
rs747010028 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499280 | CTATATAAATGCAAC[C/T]GGCGTTCTAAAATAT | 2074 |
rs747018375 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468682 | CATACATCTATTTCC[C/T]GATACTATTGGCTAC | 2074 |
rs747021788 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459249 | CCTATAAAAAGAAGA[C/T]CACTATACTGATATA | 2074 |
rs747042543 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537992 | CTCCCAACAACGTGC[A/G]TAACTTTTAAGACTA | 2074 |
rs747057220 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529474 | TAGAAGCCCAAGAAG[A/G]TCTCTGCACATCAAT | 2074 |
rs747060703 | snp | G/T | 1.65669e-05 | 0.00287805 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516034 | AACTGAGCTTATCAA[G/T]AAGTGCAATACTGGT | 2074 |
rs747107003 | snp | C/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540163 | CCTGCCTCAGCCTGC[C/T]GGGTAGCTGGGATTA | 2074 |
rs747112820 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454494 | TCTTGAATAAGCGTT[A/G]CTTTATTCTACATGC | 2074 |
rs747160423 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511689 | CCTTGCCTTCCAAAG[C/T]GCTAGGATTGCAGGC | 2074 |
rs747193669 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467162 | GATTTCTACATTTTT[-/G]GCTATTACTAATAAA | 2074 |
rs747201074 | snp | C/T | 1.64833e-05 | 0.00287078 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49524015 | AGTACAATGTATTTA[C/T]AATCCCCACAGACCG | 2074 |
rs747204355 | snp | A/G | 4.94254e-05 | 0.00497094 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49483450 | TGTCATCCTGCATCA[A/G]TCGAATGTAGGAGTA | 2074 |
rs747219961 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498236 | ACAGAGACACTGTTC[C/G]CATTTCAATGTTCAT | 2074 |
rs747223564 | snp | A/C/T | 3.30487e-05 | 0.00406491 | missense | ERCC6 | GRCh38.p7 | 10:49470869 | GATGGCATTTGGGTG[A/C/T]CTGAACATCTGATCC | 2074 |
rs747263126 | snp | C/G | 1.65181e-05 | 0.00287381 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474013 | TGTTTCCCGTCTGAA[C/G]TCTGTGCACTCACCT | 2074 |
rs747281946 | snp | C/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519917 | CTGCCTCAGACTCCC[C/G]ACGCTGAGCCCAGGC | 2074 |
rs747294096 | snp | A/G | 6.59131e-05 | 0.0057404 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516716 | TACGGTGAAGAAATC[A/G]TTTGGTGGTGCTGTA | 2074 |
rs747294409 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523637 | AAAATTACTTTCCTG[C/T]TTCAAAAGGGAAAAC | 2074 |
rs747296415 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510887 | TCCTTCTACCCATAT[A/G]ACTTTAAAGCACTGC | 2074 |
rs747338386 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506387 | TGAGTGTCTTCACAA[C/T]CGCAATACTATGTAA | 2074 |
rs747413351 | snp | C/G | 3.30382e-05 | 0.00406423 | missense | ERCC6 | GRCh38.p7 | 10:49473007 | CCCGCGTGGTCAGAA[C/G]AAACACAAATATGGA | 2074 |
rs747436506 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518793 | CAGGGGAAGGACAAT[A/G]AAGAGTATTATCTTC | 2074 |
rs747451736 | snp | A/C | 1.65438e-05 | 0.00287605 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524685 | GAGGGATCTGGGTAC[A/C]AAAAGGTGTCATCTG | 2074 |
rs747472833 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494956 | GTACCATACATTTGT[C/G]AATGTTTAACCCAAT | 2074 |
rs747474215 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486093 | AATGGGGATGCCACA[A/G]TAAGAAAAAAGAACC | 2074 |
rs747497870 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473611 | AGGTGGGGGATAGGA[A/G]TTTGCAAAGCAAATA | 2074 |
rs747517395 | snp | G/T | 1.65004e-05 | 0.00287227 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478510 | CATTACTATATATGT[G/T]TAAGGAACGCATTTG | 2074 |
rs747526005 | snp | G/T | 1.64819e-05 | 0.00287066 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516636 | TATAAGTTGGAGTAC[G/T]TGACAATGAGTTCAA | 2074 |
rs747529731 | in-del | -/TGTTAATG | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49466014 | TGTCTTTTGTTACTA[-/TGTTAATG]TGTTAATGTGTTACT | 2074 |
rs747536251 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487936 | AGCCACTGGGCAAAA[C/T]CCCATCTAAGACTAT | 2074 |
rs747541056 | snp | A/G | 1.65575e-05 | 0.00287724 | missense | ERCC6 | GRCh38.p7 | 10:49461448 | CGAGAGAGCCTCAGT[A/G]CTTTCAGGGCATCCT | 2074 |
rs747545407 | snp | C/T | 3.29549e-05 | 0.00405911 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524438 | TGGAGTTTCTTGATG[C/T]GCTTTTTCAAACGCT | 2074 |
rs747564424 | snp | G/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455761 | AGAGATCTACAAATG[G/T]CCAATAAACATGGAA | 2074 |
rs747568593 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479109 | GTACTAAATATACGC[-/A]AAAAAAAAAAAGCCC | 2074 |
rs747581337 | snp | A/T | 1.64781e-05 | 0.00287033 | missense | ERCC6 | GRCh38.p7 | 10:49471041 | GAGTAAATAGCTCAT[A/T]GAGATCATTGGATTT | 2074 |
rs747586740 | snp | G/T | 1.64749e-05 | 0.00287005 | missense | ERCC6 | GRCh38.p7 | 10:49532900 | TCATTATTACTGACA[G/T]GTTGACTCTGTAAAC | 2074 |
rs747587683 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513690 | AACCATAAGCTCTCA[A/T]GAAAACTAACTATCG | 2074 |
rs747617503 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481372 | ATAACAGGAGATTCA[A/G]AGAAAGAAGAGACTC | 2074 |
rs747621933 | snp | A/T | 1.64746e-05 | 0.00287002 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524609 | GCTTGATCTGCCAAA[A/T]ACTTTTCGAAGCCTG | 2074 |
rs747651923 | in-del | -/TATT | 1.65119e-05 | 0.00287327 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49471092 | GGTCTTTTAGCACTC[-/TATT]TGTCAAAAACTGCTT | 2074 |
rs747676022 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525383 | GCTACACGTGACTAA[C/T]GGCTACTATAATGGG | 2074 |
rs747681628 | in-del | -/C | 1.6574e-05 | 0.00287867 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49474216 | TGGTTGCAAATTTTT[-/C]CTTAGGGCTATAAGT | 2074 |
rs747729450 | snp | C/T | 1.6784e-05 | 0.00289685 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461329 | TGGACTCCTTGCAAG[C/T]ATGGCATGCAGCAAT | 2074 |
rs747761714 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475309 | ATGAAATAAAATATA[C/T]ATCAAAATTAATTTC | 2074 |
rs747799760 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463729 | TGTTCTCATGAGTGA[A/G]TGAGTTTCATGAGAT | 2074 |
rs747814000 | snp | C/T | 1.66147e-05 | 0.0028822 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524282 | ACCTCGTCATCTTCC[C/T]CCTCTTCCTCCTCCT | 2074 |
rs747816607 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462808 | TTGGGAAAAATTAAA[A/C]GTGTAACACCACACT | 2074 |
rs747833717 | snp | G/T | 1.64789e-05 | 0.0028704 | missense | ERCC6 | GRCh38.p7 | 10:49470754 | TCAGATTTCTCTTCA[G/T]ATGATGTGGCATCAT | 2074 |
rs747836397 | snp | A/C/T | 3.30613e-05 | 0.00406568 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49493237 | GACAATTACAGTTGG[A/C/T]CCCAACCCCTCAAAC | 2074 |
rs747845438 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489663 | ACTACTAGAGACTAC[A/G]TAGCAAAAAAAGGTA | 2074 |
rs747871555 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530705 | AATGCAATACTGAAT[A/G]TTATTCTGAATCACC | 2074 |
rs747872525 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49493913 | CCTGGGAAGCCCACA[A/C]CGACAGTGTACAAGC | 2074 |
rs747903426 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant, stop-gained | ERCC6, PGBD3 | GRCh38.p7 | 10:49515428 | GACATTCAGCGCATC[A/G]CGTTTGCTTTCCCTG | 2074 |
rs747941045 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49458991 | TGTGGGCCTGGAAAG[C/T]GATGAAGTTTCTCAT | 2074 |
rs747950488 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457236 | AGACTTATTGGCCTA[C/T]TTAAAAATTCTTTCT | 2074 |
rs748001112 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502129 | TCTCATTTTGGACTT[C/T]AGCTCATTTAACTGG | 2074 |
rs748010976 | snp | A/T | 2.37318e-05 | 0.00344461 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472888 | CTAATACATTCTTTT[A/T]AAAAAAAAATAAAAA | 2074 |
rs748033001 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | ERCC6 | GRCh38.p7 | 10:49470406 | ACACTATGATGTTTT[C/G]TTTTTGACTTGTGCT | 2074 |
rs748053648 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457672 | AAGAAACAAACTGCA[C/T]TAAGACAGCTAAGAA | 2074 |
rs748104956 | snp | C/T | 1.64925e-05 | 0.00287158 | missense | ERCC6 | GRCh38.p7 | 10:49472452 | TCTTCTGGCCTATTC[C/T]CCATGCTCGCTCCCG | 2074 |
rs748108036 | snp | A/C | 1.65496e-05 | 0.00287655 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506029 | TACCATGAAAATAAA[A/C]ATCACATTTCCATTA | 2074 |
rs748113932 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510775 | CACAGACAGAGAAGC[A/G]TGACTTGAAAATGGT | 2074 |
rs748122602 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529662 | AATAAAAGGAGGGCC[A/G]CGTGAACTGAACCAA | 2074 |
rs748127078 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469247 | ATTAACCTTAGCATT[C/G]AGAAACCTGGCAGAC | 2074 |
rs748130314 | snp | C/T | 8.25702e-05 | 0.00642482 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478518 | TATATGTTTAAGGAA[C/T]GCATTTGTTCTTACC | 2074 |
rs748155151 | snp | A/C | 1.6591e-05 | 0.00288015 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516425 | TGCATTGTCAGCAAC[A/C]TGCAAATTAGAAAAT | 2074 |
rs748160577 | snp | G/T | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539133 | TGGCGCATGCGCCTG[G/T]CTCAGCGTTTGTTTT | 2074 |
rs748176822 | snp | A/C | 0.000347633 | 0.0131794 | missense | ERCC6 | GRCh38.p7 | 10:49505905 | AGCTTTTTGAACAGA[A/C]AACCTGGCACTTTAA | 2074 |
rs748181487 | snp | C/T | 0.000215709 | 0.0103831 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524697 | TACCAAAAGGTGTCA[C/T]CTGGCCAGTGCGGAT | 2074 |
rs748200205 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463521 | GAAGATAATATAGTA[C/T]ACAACCTTTTGTGTA | 2074 |
rs748213769 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478191 | TCAAAGCCTGTGGAC[C/T]AGAGAAGAATCCACT | 2074 |
rs748229311 | snp | A/T | 1.64746e-05 | 0.00287002 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470195 | ACCTGATTTTTTGAA[A/T]AGCTTTTCCAAAACA | 2074 |
rs748250898 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49471051 | CTCATAGAGATCATT[A/G]GATTTGAAAAACCGC | 2074 |
rs748261677 | snp | G/T | 1.64765e-05 | 0.00287019 | missense | ERCC6 | GRCh38.p7 | 10:49532927 | AAACAGTCTTGCTCC[G/T]GAGTTTGACTTGAGT | 2074 |
rs748275893 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465063 | CCATGCACCTGGAAA[A/G]GCTGCAGACACTCAA | 2074 |
rs748288067 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465657 | TTGGGTCTTTCCTGT[C/G]CTGTTCTTGTACTAG | 2074 |
rs748294679 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509638 | TAACAAAAATAGATA[C/G]AGATTGACTTAAAAT | 2074 |
rs748342074 | snp | C/T | 1.66565e-05 | 0.00288583 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516154 | CATATTCCTCATGTT[C/T]AGTATTTGGGTTTTT | 2074 |
rs748391078 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498158 | TCTAGAAACACACAT[-/A]CAACACACATTTTTT | 2074 |
rs748391653 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49530353 | CCTCTGGACTTAACT[A/G]TGGTTTGACTTACAA | 2074 |
rs748393109 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507640 | TGTACAACAATCGTT[C/T]TTGACAGGGGGCAAT | 2074 |
rs748393292 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536742 | TCCAGGGCTGAACAA[A/T]CTCCTCCTTCAGTAG | 2074 |
rs748403975 | snp | A/G | 1.64931e-05 | 0.00287163 | missense | ERCC6 | GRCh38.p7 | 10:49532555 | CACGTGAGGTCATCC[A/G]GGACCGACCGATACT | 2074 |
rs748412731 | snp | A/G | 1.66646e-05 | 0.00288652 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474248 | CGGAGAAAATCTGTG[A/G]TAAGAAAGAGTACAT | 2074 |
rs748423645 | snp | C/G | 1.64936e-05 | 0.00287168 | splice-donor-variant | ERCC6 | GRCh38.p7 | 10:49470974 | TGATTTTATGTAATA[C/G]CTGCAAAAATTGCAC | 2074 |
rs748428006 | snp | C/T | 4.97872e-05 | 0.0049891 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516060 | CTGGTGAAAAAGTTA[C/T]TGAATACAAAATGGT | 2074 |
rs748447807 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521273 | TTTATCACCCTGAAG[A/G]GGAAAGGTTCACATG | 2074 |
rs748502209 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49473518 | GTCTTGAAGCTATTG[C/T]AGTGGTACCATCCAT | 2074 |
rs748511167 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480827 | AATCATGAAGAAATG[-/T]TAAGGCAAACCCAAA | 2074 |
rs748628170 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499212 | CTTGTAACAACAACA[A/C]CACGATGTTTAGCAT | 2074 |
rs748678588 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492278 | GCAGCCGGCACTGCT[C/T]TCCTGGGCCCCGAGA | 2074 |
rs748710425 | snp | C/T | 1.65329e-05 | 0.0028751 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516578 | CAGAAAACATTTGAA[C/T]TCAGAGCTAGTCAAG | 2074 |
rs748731504 | snp | A/G | 1.77385e-05 | 0.00297808 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524799 | GAACAATAGCAATGC[A/G]TTTCGCACTAGCATG | 2074 |
rs748783305 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456882 | ACTGAGACACCACCT[C/T]CCCAAGATCATGGTA | 2074 |
rs748791839 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523865 | CAGCATCATTAAGGA[C/T]TCAGGGGCCCCACTG | 2074 |
rs748795613 | snp | C/T | 1.70589e-05 | 0.00292047 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515358 | TGATATTCAACGGAA[C/T]ACTTCACATGTAAGG | 2074 |
rs748806326 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535221 | CAAAAAGGAAGCAGA[C/T]AGGAAGCAGGACTGG | 2074 |
rs748846798 | snp | A/G | 1.80569e-05 | 0.00300468 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472899 | TTTTAAAAAAAAAAT[A/G]AAAACAAACCTGCGT | 2074 |
rs748886593 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461647 | CAGTACTGTAGTAGA[A/C]AAAAACAAAGTGATA | 2074 |
rs748890892 | in-del | -/TTAA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512066 | AAAGATTGAGAAATT[-/TTAA]TTAATTGCAGGTTAA | 2074 |
rs748906719 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473325 | ATATCCAGAAGTAGG[A/G]CATAGAGTTAAAAAC | 2074 |
rs748914335 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524569 | TTTATTACAACCTTG[C/T]TTCTTCCTTTCAAAA | 2074 |
rs748921820 | snp | A/C | 0.000313736 | 0.0125208 | missense | ERCC6 | GRCh38.p7 | 10:49505965 | TCAGAATCGTCCTCC[A/C]GCTTCAGACGTTTCT | 2074 |
rs748948969 | snp | A/G | 3.31071e-05 | 0.00406847 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516460 | TTTCAAACCGGTCAC[A/G]TCTCATGGCAGCACT | 2074 |
rs748973088 | snp | A/G | 1.64947e-05 | 0.00287177 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49500540 | GAGGAGCACTTGCCT[A/G]TAATTTGAACCACGA | 2074 |
rs748980601 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49500573 | CCTGATCTTGCTGTA[A/G]CTCAGACCTGCCAAG | 2074 |
rs749046917 | snp | A/C | 1.64762e-05 | 0.00287016 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524037 | CACAGACCGACCTTA[A/C]CCGCTGCTTATAATA | 2074 |
rs749051037 | snp | G/T | | | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514794 | TTGCATTCTGTAGTA[G/T]GATAGGTTTTCTATT | 2074 |
rs749055573 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511309 | AAACTATATTTACAT[C/T]ACTAGGAAGGAAATA | 2074 |
rs749060162 | snp | C/T | 3.38644e-05 | 0.00411474 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517114 | TTAGTGTTCGAGGCA[C/T]CTTGGGACTAAAACG | 2074 |
rs749066317 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513441 | CATTTATTAATTCAT[C/T]TAATCTTTACAACCT | 2074 |
rs749095929 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481861 | AGACCACCACCCAAG[A/G]TCAGGTCCAGGTCCT | 2074 |
rs749108144 | in-del | -/CA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464768 | AGCCTTGGGAGCTTC[-/CA]CACAGTGTTGAGCCT | 2074 |
rs749121857 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468944 | AAATCTAAGACAATA[C/T]GAGCATCATAATACC | 2074 |
rs749129458 | snp | G/T | 1.64765e-05 | 0.00287019 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49530813 | TTCAATAATTTTATT[G/T]ATTTGCCTTAGGGAT | 2074 |
rs749142673 | in-del | -/T | 4.94874e-05 | 0.00497406 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473637 | AATACACATTCCCAG[-/T]TGAGTGCTTCTCTAT | 2074 |
rs749165520 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481264 | TGAAGTGTTAAGAAG[C/G]TTTTCTTGTTTGTTT | 2074 |
rs749166731 | snp | A/C | 1.64972e-05 | 0.00287199 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470501 | TTCTCTTTTGTAAGA[A/C]AGACCTAACTTTTCA | 2074 |
rs749184579 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494716 | GGCAAGACTGACCAA[A/C]TTTGTAAGGAAAAAT | 2074 |
rs749211696 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467688 | CTCCCAGCTCAGCCT[C/T]GCAAGTAGCTGGGAC | 2074 |
rs749223591 | snp | G/T | 1.64749e-05 | 0.00287005 | missense | ERCC6 | GRCh38.p7 | 10:49530722 | TATTCTGAATCACCT[G/T]ATTATACTTCTGTCG | 2074 |
rs749264257 | in-del | -/TTAAA | 1.65226e-05 | 0.0028742 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470949 | GTGCAATTGATTACT[-/TTAAA]TTAAATGATTTTATG | 2074 |
rs749299278 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489845 | ACTGCCTTCTTTATC[A/T]CTTCATTTACTACAT | 2074 |
rs749316600 | snp | A/C/G | 3.29523e-05 | 0.00405898 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516859 | GAACTTCATCAGGAG[A/C/G]GTCATCTTTAGGTGC | 2074 |
rs749319221 | snp | A/G | 1.64792e-05 | 0.00287042 | missense | ERCC6 | GRCh38.p7 | 10:49528437 | TCCTCCTCCAGACTG[A/G]CGTGATCTAGTTCAA | 2074 |
rs749367192 | snp | C/T | 1.65192e-05 | 0.00287391 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458806 | TGAAAGTTTAGGAAG[C/T]AATGTTGTTTAGCAG | 2074 |
rs749392467 | snp | C/T | 4.962e-05 | 0.00498072 | missense | ERCC6 | GRCh38.p7 | 10:49505927 | GCACTTTAAAACCTT[C/T]GTCAAATTCAGCATC | 2074 |
rs749408119 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520260 | CTTCCTAAGTCAGCG[C/T]CTCCAGTGTTAGGGG | 2074 |
rs749502916 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489527 | ACCCTGGTCTTGTAA[C/G]CACAAAACCAATGCA | 2074 |
rs749503929 | snp | A/G | 0.000132096 | 0.00812592 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49505985 | CAGACGTTTCTCTTT[A/G]TCCTGCAGTCTCAGT | 2074 |
rs749505894 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482750 | GAACTGCTCCATAAA[C/T]ACAGGCAACGTGCCT | 2074 |
rs749509602 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458800 | GGGACTTGAAAGTTT[A/G]GGAAGCAATGTTGTT | 2074 |
rs749555462 | snp | A/T | 2.33408e-05 | 0.00341611 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461565 | ACGCCAACTAGCAAG[A/T]AAAGAAATAGCAAAG | 2074 |
rs749556242 | snp | G/T | 3.30568e-05 | 0.00406538 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472334 | TTCCCTGCTCAAGAC[G/T]CTGGGAACGCACAGC | 2074 |
rs749568055 | snp | A/G | 1.65855e-05 | 0.00287967 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493255 | CAACCCCTCAAACCT[A/G]CATCCAAACGTCCAA | 2074 |
rs749593091 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488600 | TGTACTCAGAATGTG[C/T]CTGAAATATTTCAGA | 2074 |
rs749609902 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497651 | GACAATCAACTCCAT[C/T]AACAGTCACATCGTC | 2074 |
rs749619397 | snp | A/G | | | missense | ERCC6 | GRCh38.p7 | 10:49482826 | AGGTTATTTTGCATC[A/G]GTGAGCCAGACAGAA | 2074 |
rs749626127 | in-del | -/ATTTT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499020 | TGAAACAGAAAAAGC[-/ATTTT]ATTTGAAACAGAAAA | 2074 |
rs749647738 | in-del | -/GTTGTGTTCTTAT | 1.65119e-05 | 0.00287327 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49515400 | TTTTCACATCGAAAA[-/GTTGTGTTCTTAT]GACATTCAGCGCATC | 2074 |
rs749663866 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527861 | GTACACACACACACA[A/C]ATACACACACACAAT | 2074 |
rs749674398 | snp | C/G | 1.65059e-05 | 0.00287275 | missense | ERCC6 | GRCh38.p7 | 10:49470844 | AAGGCTGGTTGAATC[C/G]TTCTTTTTAGATGGC | 2074 |
rs749674727 | snp | A/G | | | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49538985 | GCGCGAGCGCCCACA[A/G]GGAAACAGAGACGCT | 2074 |
rs749684378 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488659 | TTTTTTTTTTTTTTT[-/A]AAGTTTTTTACTCCC | 2074 |
rs749767206 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510697 | TATAATGCCTCCTCA[A/T]GGCAGACCGTTAAGT | 2074 |
rs749797496 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464953 | GGGTTGGAGTCCCCA[A/C]ACAGAGTCCCTACTG | 2074 |
rs749825089 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477101 | ATCTTCCACAAGCCC[A/G]GAGCAACTGTGCCCA | 2074 |
rs749853726 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509366 | AGAGAAAGCAAGTTA[C/T]GTATGTGGCCCAATG | 2074 |
rs749872100 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516938 | AAGATACGCAGCTGT[A/G]TGCAACAAAGAACCT | 2074 |
rs749872255 | snp | C/T | 3.2956e-05 | 0.00405918 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515694 | CCACGGATTGATGCC[C/T]GATACTTATCAATGT | 2074 |
rs749883507 | snp | A/G/T | 4.94306e-05 | 0.00497124 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516820 | TCCTTGATGGTGGAG[A/G/T]TTGCTGCACAGTAAA | 2074 |
rs749929693 | in-del | -/C | | | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49539075 | CAACCATAGACACCG[-/C]CCCCAACAGCGACTC | 2074 |
rs749963470 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473429 | CTTAGTCCTTTCCCT[C/T]CACGTACAGCAGCAC | 2074 |
rs749971810 | in-del | -/TGA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533259 | ACCAAAATCCTGGGG[-/TGA]TGGCCATGGAATATT | 2074 |
rs749984378 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49530234 | CACCAAAAAGGAACT[C/T]TTCTCAAATACACAG | 2074 |
rs749990266 | snp | A/C | 1.64781e-05 | 0.00287033 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470150 | ATTTTCTAATCCTAG[A/C]ATCCCTGTGGCAAAC | 2074 |
rs749996750 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | ERCC6 | GRCh38.p7 | 10:49482794 | AGATGAAGTCAAAGA[A/G]CGACCACAGCTCTCG | 2074 |
rs750016520 | snp | A/G | 1.74665e-05 | 0.00295515 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524788 | CGGCTCTGAAAGAAC[A/G]ATAGCAATGCGTTTC | 2074 |
rs750056563 | in-del | -/A | 1.68553e-05 | 0.00290299 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532981 | CTCTACAGACTACCT[-/A]AAAGGAAAAAAATTT | 2074 |
rs750079035 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455253 | AAATTTCATCCAAGA[A/G]TATAAAAGACTTTAA | 2074 |
rs750083678 | snp | C/T | | | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454234 | ATCTACTATTGAACC[C/T]CTTTAGTGCATTTTT | 2074 |
rs750084326 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498924 | AAGAGTCCTAGAAAC[C/T]ATTTGGAGGAGTTTG | 2074 |
rs750088876 | snp | C/T | 1.65201e-05 | 0.00287398 | missense | ERCC6 | GRCh38.p7 | 10:49505957 | CACTTTCCTCAGAAT[C/T]GTCCTCCAGCTTCAG | 2074 |
rs750098799 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456610 | TGGGGAGGCAGACTA[C/T]TGCTTGAACATTTTT | 2074 |
rs750147682 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537889 | CATCATGCCCGGCTA[A/C]TTTTTCGTATTTAGT | 2074 |
rs750192673 | snp | C/G | 1.73315e-05 | 0.00294371 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460503 | TGCTTTTGAGACTTA[C/G]AGATCAAAATATTCT | 2074 |
rs750222428 | snp | C/T | 1.64969e-05 | 0.00287196 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49493189 | CCACGTGTGAAATTC[C/T]TTCACCCACTGATGC | 2074 |
rs750246054 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485250 | CTGGGGCTTGGAAAT[-/G]GTAACTAATGTACCA | 2074 |
rs750284305 | snp | A/C | 1.68798e-05 | 0.0029051 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460325 | AATTTTCACAGCATT[A/C]AATCAAGCAAGTCTC | 2074 |
rs750307995 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475354 | TTCCTTTTTAATGTG[A/C]CTACTAGAAAATTTA | 2074 |
rs750313950 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470720 | AGAAGTTACTGCATT[C/T]ACTTCAGCTCCTTTA | 2074 |
rs750361952 | snp | C/T | 3.29554e-05 | 0.00405914 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515662 | AGAACAAAAGAGGGC[C/T]TGAATACCATTTCTT | 2074 |
rs750364051 | snp | A/T | 4.94303e-05 | 0.00497119 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516892 | ATGAGGGATCATCTG[A/T]GTCAGACTCAGCATC | 2074 |
rs750366811 | snp | C/T | 3.29565e-05 | 0.00405921 | missense | ERCC6 | GRCh38.p7 | 10:49532598 | CAACGAGCTGGGAGG[C/T]ACGGCTGGCCTCATG | 2074 |
rs750401832 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49473494 | CATTGTATCTCGTAA[C/T]CAGTGGCTGTCTTGA | 2074 |
rs750464264 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | ERCC6 | GRCh38.p7 | 10:49530779 | TGTCTCTGCTGGTGG[C/T]AGCTTGAGGGCTAAG | 2074 |
rs750518707 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515498 | AATGTTACGCTTCTG[A/G]GGTCTTCCTTTTTGG | 2074 |
rs750554118 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | ERCC6 | GRCh38.p7 | 10:49483432 | GCCAGTCATACCTGC[C/T]AATGTCATCCTGCAT | 2074 |
rs750598605 | in-del | -/TATAGGAACCGGTTTCA | 1.65087e-05 | 0.00287299 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49493128 | TTACCTTTTTGTGGG[-/TATAGGAACCGGTTTCA]TGTAGAATTGCCACT | 2074 |
rs750622573 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519396 | TAGAAAATAAAAACA[C/T]AAAAGAGGTCATTTT | 2074 |
rs750626920 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495819 | TCCGTCTACACTGTT[A/G]CTATGCCAGGTCCAG | 2074 |
rs750638927 | snp | A/G | 1.92476e-05 | 0.00310217 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472880 | TATTTCTACTAATAC[A/G]TTCTTTTAAAAAAAA | 2074 |
rs750643538 | snp | A/G | 3.29712e-05 | 0.00406011 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515420 | GTTCTTATGACATTC[A/G]GCGCATCGCGTTTGC | 2074 |
rs750653279 | in-del | -/C | 9.88875e-05 | 0.00703093 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473429 | CTTAGTCCTTTCCCT[-/C]CACGTACAGCAGCAC | 2074 |
rs750657678 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480979 | AATATGAGTGATTAT[A/G]GACTAGATAACAGAC | 2074 |
rs750668898 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526206 | GTCAGTTTTCCAAAG[C/T]GTTACGTTCCAAAGT | 2074 |
rs750735670 | snp | C/T | 3.29506e-05 | 0.00405884 | missense | ERCC6 | GRCh38.p7 | 10:49532878 | TTCTTGCTTGATTGC[C/T]ATTTCTTCATTATTA | 2074 |
rs750751680 | snp | A/T | 1.67508e-05 | 0.00289398 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471147 | AAAGATAAGCTGGTA[A/T]AAAACAATGTGTAGC | 2074 |
rs750753764 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528686 | ACTAGAGAGCCCTAT[A/G]TGAGCAACTACCACT | 2074 |
rs750793645 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476915 | ACCTACCTGGACCCC[C/T]TTCAACCCCCTGCAT | 2074 |
rs750816798 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533407 | CGATGTTAGGAAAGA[A/G]CTTCTGTGTGAATCT | 2074 |
rs750816875 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521029 | CTCCCAAATGCCTCA[A/G]TCTGAATTCATTATT | 2074 |
rs750846256 | snp | A/G | 3.32989e-05 | 0.00408024 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516129 | TGAAGGACAAGTGAC[A/G]CACCGACACCATATT | 2074 |
rs750847496 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499557 | GTCTGAGGTTTCCTG[C/G]GCACACCCCTCTAGC | 2074 |
rs750861299 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491567 | TCTCTTCTTAGAAGT[A/T]TGCCCTCCAAAGTCA | 2074 |
rs750881503 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459715 | TACATCTAATGCAAC[G/T]TGCCTTAAAAAAACA | 2074 |
rs750889552 | snp | C/T | 3.30273e-05 | 0.00406356 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516001 | TTCTCACTGTACCTG[C/T]TGCCTGATGTCCCAT | 2074 |
rs750901864 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471152 | TAAGCTGGTATAAAA[C/T]AATGTGTAGCTCTAC | 2074 |
rs750905840 | snp | C/T | 4.94654e-05 | 0.00497295 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49524007 | AAGCAAACAGTACAA[C/T]GTATTTATAATCCCC | 2074 |
rs750916757 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | ERCC6 | GRCh38.p7 | 10:49459147 | GTGAGGAGGAAGCGA[A/G]GGGCCCGGATGAAGA | 2074 |
rs750926503 | snp | G/T | 4.55456e-05 | 0.00477187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488159 | TTAGCCTGACTTACT[G/T]AATGCAGTGCTGTTG | 2074 |
rs750935024 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501712 | GTAAATCCCAGCACT[G/T]TGGGAAGCCGAGGCA | 2074 |
rs750935710 | snp | C/T | 4.94303e-05 | 0.00497119 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524090 | TATCTTCCCACTTTC[C/T]GACCTCCTCCTCCTC | 2074 |
rs750945881 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | ERCC6 | GRCh38.p7 | 10:49474088 | CATATTTTCAACAAA[A/G]ACTCAACAACAATCA | 2074 |
rs750959894 | snp | A/C | | | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49471024 | TGCATCAGGACTAGT[A/C]AGAGTAAATAGCTCA | 2074 |
rs750973346 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502707 | GGTAATTCTTCTCCC[C/T]ATGGGACATTTGGCA | 2074 |
rs750977355 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528870 | CCCTTACACACTGGG[C/T]AAATCCCTAAACTAC | 2074 |
rs750978636 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458503 | AACTGTGCTCCCTGA[C/T]AGCATCTTTTGGGTA | 2074 |
rs751032614 | snp | C/T | 4.94417e-05 | 0.00497176 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49517028 | TGTAGCATTTTCAGG[C/T]GGTTGTATCACTATA | 2074 |
rs751043899 | snp | A/G | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540574 | AAAGGGGAAGTTGAG[A/G]GTTATTATTTACAAA | 2074 |
rs751088999 | in-del | -/T | 1.6477e-05 | 0.00287024 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49516866 | ATCAGGAGAGTCATC[-/T]TTAGGTGCGTATGAG | 2074 |
rs751115103 | snp | A/G | 4.95798e-05 | 0.0049787 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482875 | GAAACTATTTGAGGA[A/G]AGGAAGCACCTTTTT | 2074 |
rs751141428 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516917 | AGCATCAGAGCCATC[C/T]TGAATAAGATACGCA | 2074 |
rs751148156 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | ERCC6 | GRCh38.p7 | 10:49539510 | GAGCTGTCCTGCTTC[G/T]CTGTTCCCCCTCCGC | 2074 |
rs751172484 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510636 | GGACTGGAAGCCACC[G/T]GGGGACAAACACTGT | 2074 |
rs751182938 | snp | A/C | 1.6489e-05 | 0.00287128 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473628 | TTGCAAAGCAAATAC[A/C]CATTCCCAGTGAGTG | 2074 |
rs751194645 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464595 | CCCATCACAGGCCCA[C/G]AGGCCCAGGGGGAAA | 2074 |
rs751201355 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | ERCC6 | GRCh38.p7 | 10:49473503 | TCGTAATCAGTGGCT[C/G]TCTTGAAGCTATTGT | 2074 |
rs751227370 | snp | A/G | 1.65512e-05 | 0.00287669 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528392 | CAATTCAAGAACACA[A/G]AGAAACTGCTCCTAG | 2074 |
rs751249194 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477997 | CCCTCAAGAATAAAT[A/G]TGAGTCCCCATGAGA | 2074 |
rs751279337 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523250 | GAGACTTGAAATGCG[C/T]GGCAGTAGCACAGTG | 2074 |
rs751292948 | snp | C/G | 1.64784e-05 | 0.00287035 | missense | ERCC6 | GRCh38.p7 | 10:49482798 | GAAGTCAAAGAGCGA[C/G]CACAGCTCTCGGAGG | 2074 |
rs751294088 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510525 | TGTCTTCCAAGGGCC[A/C]TCCCAATCCCGTGAC | 2074 |
rs751306410 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534865 | AAATAAGCCCAGCAA[C/T]AAAGCACCGGGATAC | 2074 |
rs751330876 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521463 | GTGCAAAGCAGTAGT[A/G]TATTTTAAGAAAGCA | 2074 |
rs751348434 | snp | A/G | 1.65985e-05 | 0.00288079 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516400 | AAAATTTGTCCACTG[A/G]ATCCAAATTTGCATT | 2074 |
rs751353976 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49478374 | CATTTTTATCTGGCA[A/G]AGAAAGGCTCATCTT | 2074 |
rs751390320 | snp | A/G | | | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461446 | GACGAGAGAGCCTCA[A/G]TGCTTTCAGGGCATC | 2074 |
rs751409094 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488642 | TAATGTGGCCTCTTT[-/C]TTTTTTTTTTTTTTT | 2074 |
rs751448793 | snp | A/G | 3.29696e-05 | 0.00406001 | stop-gained | ERCC6 | GRCh38.p7 | 10:49474056 | AAAACAGCAATACTC[A/G]CTGACCCTGCTTGTG | 2074 |
rs751464057 | snp | C/T | 5.06684e-05 | 0.00503305 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461313 | TCTAGCCTTAGTTGT[C/T]TGGACTCCTTGCAAG | 2074 |
rs751489733 | snp | A/C | 1.65198e-05 | 0.00287395 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500496 | ATCTGATGAAATATT[A/C]ATTGAGCTCCACAGA | 2074 |
rs751497985 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465156 | CCCAAGACCATAGGA[A/T]CCCACCTCTTGCATC | 2074 |
rs751502384 | snp | A/G | 1.64923e-05 | 0.00287156 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515825 | ACTGACAAGACACAG[A/G]GGATGGATACCAGCA | 2074 |
rs751537202 | in-del | -/AAGGGGCTG | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533696 | TAGTCCCAGTTACTC[-/AAGGGGCTG]AGGCAGGAGGATCAC | 2074 |
rs751556738 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485374 | TCCTACTAAAATATA[A/G]AAGAAAAAGTTTAAA | 2074 |
rs751572646 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | ERCC6 | GRCh38.p7 | 10:49532658 | CCTGTTCCAGCACGT[C/T]CTGGTCATAGACGTC | 2074 |
rs751598627 | snp | C/G | 6.58979e-05 | 0.00573974 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524100 | CTTTCCGACCTCCTC[C/G]TCCTCCTTCTCCTAC | 2074 |
rs751610688 | in-del | -/CTC | 1.6476e-05 | 0.00287014 | cds-indel | ERCC6 | GRCh38.p7 | 10:49532836 | ACGAAAGGAGAGGTA[-/CTC]CTCCACCTCCCCATC | 2074 |
rs751617716 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499473 | GAGTAGGAAGAACTT[C/T]CGGCAGTTGCTGACT | 2074 |
rs751623760 | in-del | -/TGGGTCATAGA | 3.31669e-05 | 0.00407215 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49472936 | GCTTGGGTTCCAGTC[-/TGGGTCATAGA]TGACAACTCTGTTTG | 2074 |
rs751643032 | snp | A/C | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525784 | ACAGAATTACTAGCA[A/C]CACCAGATGAGCCCT | 2074 |
rs751666822 | snp | G/T | 3.29554e-05 | 0.00405914 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459157 | AGCGAGGGGCCCGGA[G/T]GAAGAGTCTGCATCT | 2074 |
rs751679682 | in-del | -/CAGG | 1.64874e-05 | 0.00287113 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49470430 | TGTGCTTATAAAAAT[-/CAGG]TATTTTCCATTTGTT | 2074 |
rs751703364 | snp | C/T | 9.96761e-05 | 0.0070589 | missense | ERCC6 | GRCh38.p7 | 10:49474233 | TTAGGGCTATAAGTC[C/T]GGAGAAAATCTGTGG | 2074 |
rs751733950 | snp | G/T | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539312 | TGGCAAGGCAGTTAT[G/T]AAAGTTAAGACATAT | 2074 |
rs751758509 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470606 | AATCACTGACAACTC[C/T]TCTGGTCCAGATACT | 2074 |
rs751786734 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507003 | CAGCAACACATATAA[A/G]GCATTTATCTGCCAC | 2074 |
rs751786870 | snp | C/T | 3.30453e-05 | 0.00406467 | missense | ERCC6 | GRCh38.p7 | 10:49493233 | GACAGACAATTACAG[C/T]TGGACCCAACCCCTC | 2074 |
rs751790010 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536090 | CGCAGAACTCCAGCC[C/T]GGGCAACAAGAGTGA | 2074 |
rs751819015 | snp | C/T | 2.26278e-05 | 0.00336354 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488169 | TTACTGAATGCAGTG[C/T]TGTTGTCATTAGAAG | 2074 |
rs751832741 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489062 | TGCTGGGATTATAGG[C/T]GTGAGCCACCGTGCC | 2074 |
rs751838040 | snp | A/G | 1.6476e-05 | 0.00287014 | stop-gained | ERCC6 | GRCh38.p7 | 10:49530797 | CTTGAGGGCTAAGCT[A/G]TTCAATAATTTTATT | 2074 |
rs751839495 | snp | A/G | 4.94336e-05 | 0.00497135 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515516 | TCTTCCTTTTTGGCC[A/G]GGTTCTGGAGGATGA | 2074 |
rs751863429 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462146 | TAAAACACGCTCCAA[C/T]TACAACAGTTTGGTG | 2074 |
rs751912103 | snp | C/T | 3.53457e-05 | 0.00420376 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524796 | AAAGAACAATAGCAA[C/T]GCGTTTCGCACTAGC | 2074 |
rs751952053 | snp | C/T | 3.36751e-05 | 0.00410322 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471162 | TAAAACAATGTGTAG[C/T]TCTACCTAAAAATTC | 2074 |
rs751956414 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531288 | CACATCTGCGACAAT[A/G]TTTTTCTTCTACATA | 2074 |
rs751986947 | snp | C/T | 1.64754e-05 | 0.00287009 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470165 | CATCCCTGTGGCAAA[C/T]GTATCAAATGGATTA | 2074 |
rs752009034 | snp | C/T | 1.66145e-05 | 0.00288218 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505877 | GGAAAGAACATATGG[C/T]ACATACTTAAAAAGC | 2074 |
rs752017172 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496912 | CTACACAACTGAAAA[A/G]TAATTTGTAGTTCTA | 2074 |
rs752023217 | snp | A/G | 3.33006e-05 | 0.00408034 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516140 | TGACGCACCGACACC[A/G]TATTCCTCATGTTTA | 2074 |
rs752029606 | snp | A/G | 0.00085034 | 0.0206021 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475531 | ATGAAATAAGAAATT[A/G]TGAGAGATGGTTAAA | 2074 |
rs752059083 | snp | A/G | 8.2752e-05 | 0.00643189 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516241 | ACTTATAGCCAAACC[A/G]AATGGGCTTTCCCCG | 2074 |
rs752073309 | snp | C/T | 1.65031e-05 | 0.00287251 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524241 | AGTCAGTACCATCTC[C/T]AGACAGGTCCGCCTC | 2074 |
rs752073310 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528261 | TTTGGTTCTGCAGGT[A/G]TAGAGAATAAAATTT | 2074 |
rs752107433 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510281 | ATTTATTTTAGAAGA[A/T]TTTTCAGCATTCCAA | 2074 |
rs752117016 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49514109 | ACAAACCAAATTCTA[A/T]AACTTCAATCCAAAT | 2074 |
rs752170411 | snp | A/G | 6.58903e-05 | 0.00573941 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532691 | CACCCAAACCCTGCA[A/G]CTCAAGGGCCTGGGC | 2074 |
rs752199198 | snp | C/T | 1.65031e-05 | 0.00287251 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500523 | CAGACTGACAGTCTG[C/T]AGAGGAGCACTTGCC | 2074 |
rs752345184 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476696 | CAACCTCACCTGGAG[C/G]TCTCCCTCTCCTGGA | 2074 |
rs752363644 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475948 | GGAAGTAACAGTAAC[C/T]GCACAGCTCGCAGCT | 2074 |
rs752371354 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508936 | AACATGTCTAACCAG[A/C]CTGTACTGTAGTCTG | 2074 |
rs752401611 | snp | A/C | 3.30028e-05 | 0.00406205 | missense | ERCC6 | GRCh38.p7 | 10:49470490 | TGGCTGGGTCTTTCT[A/C]TTTTGTAAGAAAGAC | 2074 |
rs752408449 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490044 | CACGAAATATAATCA[A/G]AAAAAGGAAATCTTG | 2074 |
rs752413484 | snp | A/G | 1.6489e-05 | 0.00287128 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517041 | GGTGGTTGTATCACT[A/G]TAGCACTTGCTTCTA | 2074 |
rs752416390 | snp | C/T | 1.65679e-05 | 0.00287814 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473976 | CATTTTGTGAGTTGA[C/T]GGCTGTCATAAAGAA | 2074 |
rs752453826 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517245 | TTTCTGTATTTTCTT[G/T]TTACCGCACAATAGC | 2074 |
rs752457941 | snp | A/C | 3.30655e-05 | 0.00406591 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473050 | GTAAGACACACAACA[A/C]TGAGCACACACACTT | 2074 |
rs752463386 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520921 | TTTAGGGGCAAATGC[A/G]TAACATTGTTAATTT | 2074 |
rs752544511 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524629 | TTCGAAGCCTGATGC[C/T]TCATTAAGCATGATT | 2074 |
rs752574208 | snp | C/G/T | 4.94705e-05 | 0.00497325 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478492 | TAAGAGCAGAGAAGG[C/G/T]AACATTACTATATAT | 2074 |
rs752581351 | in-del | -/GC | 1.66521e-05 | 0.00288544 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500733 | AGAAAAGAGAAAATG[-/GC]AAATGGTGGATAATA | 2074 |
rs752582131 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471558 | CTCTCCCTGCTCCCA[A/C]CTGCAGGTCCACACT | 2074 |
rs752592129 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519198 | CCCTGTGGTCATACC[C/T]AAATATTGCACCTTC | 2074 |
rs752631489 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490643 | CAGGCATGAGCCACC[A/G]CGCCCGGACAATTTT | 2074 |
rs752631867 | in-del | -/G | 1.6591e-05 | 0.00288015 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49516427 | CATTGTCAGCAACAT[-/G]CAAATTAGAAAATAT | 2074 |
rs752638726 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527548 | GGGCATGGTGGTATG[C/T]GCCTGTAATCCAGCT | 2074 |
rs752642347 | snp | C/T | 1.67058e-05 | 0.00289009 | missense | ERCC6 | GRCh38.p7 | 10:49461479 | GGGCCACTCGGTTGG[C/T]TTCTGCCTCCACCAG | 2074 |
rs752667183 | snp | A/G | 1.65403e-05 | 0.00287574 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524348 | TCTCCCTCTGCCTCT[A/G]GCCTCATGTCTGACT | 2074 |
rs752674827 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49483873 | TTAAAACAAAAGCAA[A/G]AAAATAAGAGAAAAT | 2074 |
rs752688681 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532854 | CTCCACCTCCCCATC[A/G]CCACCACTTTCTTGC | 2074 |
rs752689734 | snp | C/T | 1.64871e-05 | 0.00287111 | missense | ERCC6 | GRCh38.p7 | 10:49472398 | AGATCTTTTCTTCAA[C/T]GGTGCCCGCAGTCAG | 2074 |
rs752712823 | snp | C/T | 1.64972e-05 | 0.00287199 | missense | ERCC6 | GRCh38.p7 | 10:49500628 | CCCAATCCCATTTCA[C/T]CTCCCAGAATTCCTC | 2074 |
rs752737151 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524547 | CTGGAGCTTTTCTAG[C/T]TGCTCTTTTATTACA | 2074 |
rs752739206 | snp | A/G | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539375 | CGAATGTAAATCCTC[A/G]CAATTAACCTTGAAC | 2074 |
rs752767075 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535836 | ACCTTGGTAAAAGAA[A/G]TTTCAGGCCAGGCTT | 2074 |
rs752788179 | snp | A/C | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525409 | ATGGGCAACACAGAG[A/C]ACATTTTCATCACTG | 2074 |
rs752849238 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492148 | CAAACCATAGATTTT[C/T]CTGAGTCACTTCTAT | 2074 |
rs752855085 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461187 | GAGGAAGGCAAAGTT[A/C]TAACAGTATTTCTCC | 2074 |
rs752856957 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534754 | AAAATCAGTCTTGCT[C/T]TTTGTTTAACTGTGA | 2074 |
rs752888214 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49472867 | AACCATGAAACTATA[C/T]TTCTACTAATACATT | 2074 |
rs752890723 | in-del | -/AA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492788 | AAGCCACTAATGCGC[-/AA]AGTCTCTCCTTACTG | 2074 |
rs752901335 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49505147 | CATCTAAGAAGCCTT[C/T]CTAAAGTATCTTGTT | 2074 |
rs752908135 | snp | C/G | 1.70145e-05 | 0.00291667 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476171 | TCCTCCCTCACTTCT[C/G]TTGGTCCACAATTCA | 2074 |
rs752919563 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503949 | AGGTCAAAAGATTGA[A/C]GTTTGTCATTTGACT | 2074 |
rs752925338 | snp | C/T | 0.000150064 | 0.0086608 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459261 | AGACCACTATACTGA[C/T]ATATTTAATTTCTAG | 2074 |
rs752971410 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468255 | GTGCAGAGCTGTCTC[C/T]GCTATCGTCTCTTGC | 2074 |
rs753046633 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | ERCC6 | GRCh38.p7 | 10:49458919 | CACAAGACTGTGATG[C/T]AGATAACTTGGATTC | 2074 |
rs753068929 | snp | C/T | 1.66001e-05 | 0.00288094 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458774 | ATAATCAGAAATGCC[C/T]GTTAGAAAAAGGGAC | 2074 |
rs753069179 | snp | A/G | 1.71858e-05 | 0.00293132 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528556 | TAGAAGACAGAAAAC[A/G]GCAATGAAGTGATTT | 2074 |
rs753096713 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470285 | ACGCCTTTTCTTCAC[C/T]AGGTGTGGAATTCGA | 2074 |
rs753128837 | snp | A/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455595 | TAGCATGTGATGAGT[A/T]GAAAGCTGACATTTT | 2074 |
rs753133270 | snp | A/G | 1.64795e-05 | 0.00287045 | missense | ERCC6 | GRCh38.p7 | 10:49482812 | ACCACAGCTCTCGGA[A/G]GTTATTTTGCATCGG | 2074 |
rs753160006 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522081 | CTACCCTGGGAACTA[C/T]TCCTAAATTCTAACC | 2074 |
rs753167318 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468153 | AGGCCTTTTCACTGA[C/T]CTTAAGTAGTTTTCT | 2074 |
rs753180733 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478239 | CGGGCCTAGCCTGCC[C/T]ACAGTTCCAGGATCA | 2074 |
rs753184026 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467275 | AAAGCTATATCACAA[A/G]GAAAGCGCATGCAAC | 2074 |
rs753191669 | snp | A/C | 1.81246e-05 | 0.00301031 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515299 | ACATAATGTATAAAA[A/C]TATGTTTCTTATCTC | 2074 |
rs753201033 | in-del | -/CAGCA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531879 | CCAACGGGGGCCAAG[-/CAGCA]CAGCAATGATAAGTG | 2074 |
rs753210106 | snp | C/T | 4.98235e-05 | 0.00499092 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516367 | CATTAAGTTTGCTTA[C/T]GAGAGGTCGCAATTT | 2074 |
rs753232818 | snp | A/G | 1.65094e-05 | 0.00287305 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528407 | GAGAAACTGCTCCTA[A/G]CATCCTCACCTGCAT | 2074 |
rs753239820 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487861 | GAATTAAAAAGATGC[C/T]TATGTAAAAAGAACA | 2074 |
rs753266801 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479589 | TACATATTATGATTT[C/T]TGATGCAGAGATGAT | 2074 |
rs753296620 | snp | C/G | 1.67725e-05 | 0.00289585 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461492 | GGCTTCTGCCTCCAC[C/G]AGTACATAATCTGGG | 2074 |
rs753301921 | snp | A/G | 3.29484e-05 | 0.00405871 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524641 | TGCTTCATTAAGCAT[A/G]ATTTTTCTGGGCTTT | 2074 |
rs753317688 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511642 | TATTGGCCAAGCTGG[G/T]CTCAGACTACTGACC | 2074 |
rs753322516 | in-del | -/T | 1.66464e-05 | 0.00288495 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470167 | TCCCTGTGGCAAACG[-/T]ATCAAATGGATTACC | 2074 |
rs753353280 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520625 | AATACCTAGCATGAA[C/T]GTTGCTAGTTCCCCA | 2074 |
rs753388562 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | ERCC6 | GRCh38.p7 | 10:49471016 | CTCTGGGATGCATCA[A/G]GACTAGTCAGAGTAA | 2074 |
rs753390576 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475468 | GGAGATTCATGGAGA[G/T]GAATAGATGTGAATG | 2074 |
rs753417618 | snp | C/G | 1.65037e-05 | 0.00287256 | missense | ERCC6 | GRCh38.p7 | 10:49500646 | CCCAGAATTCCTCCT[C/G]CCTGCTGGCAGTGCA | 2074 |
rs753428200 | snp | A/G | 1.66496e-05 | 0.00288522 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505860 | TTGATAGCAAATAGA[A/G]AGGAAAGAACATATG | 2074 |
rs753464046 | snp | G/T | 1.64749e-05 | 0.00287005 | missense | ERCC6 | GRCh38.p7 | 10:49532868 | CACCACCACTTTCTT[G/T]CTTGATTGCCATTTC | 2074 |
rs753484284 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488967 | TTTTTTGTATTTTTA[G/T]TAGAGACGGGGTTTC | 2074 |
rs753496156 | snp | C/T | 1.65173e-05 | 0.00287374 | missense | ERCC6 | GRCh38.p7 | 10:49461433 | CCCAGACACCGCTGA[C/T]GAGAGAGCCTCAGTG | 2074 |
rs753498605 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487711 | GTATACCACTGGAAT[A/G]ATGTTTAGTTTCTTA | 2074 |
rs753507224 | snp | G/T | 8.27616e-05 | 0.00643226 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532503 | TATCCCTGTCATGTT[G/T]TACCACCACTTTGAA | 2074 |
rs753540627 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501624 | GTATGAAGATTATAT[A/C]CCAAGTTACAAAATC | 2074 |
rs753551732 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49532808 | CAGAGGTGGACAGCC[C/T]GTCACCCACAGAACG | 2074 |
rs753553933 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | ERCC6 | GRCh38.p7 | 10:49459170 | GATGAAGAGTCTGCA[C/T]CTTCTGCTCTTCCAC | 2074 |
rs753581752 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456464 | ACTCAAAAATTTTAT[C/T]AGTAAAGGAAGAATG | 2074 |
rs753622223 | snp | C/G | 3.29527e-05 | 0.00405898 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515651 | CAGTTCGAAACAGAA[C/G]AAAAGAGGGCTTGAA | 2074 |
rs753645499 | in-del | -/TCATCA | 1.65201e-05 | 0.00287398 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500499 | GATGAAATATTAATT[-/TCATCA]GAGCTCCACAGACTG | 2074 |
rs753649748 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511012 | TTAGAATCTTATAAC[-/A]AAAAAAAAAAAAGAT | 2074 |
rs753706257 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49482280 | CCTTTTCTAAGTTTC[A/T]CCACTACTTTATAAG | 2074 |
rs753747220 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464318 | TTTAGGGTATCTGGC[A/G]GAAGAAATTTCTAAG | 2074 |
rs753747995 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463680 | AGGAACCCAGTGGGA[A/G]GTGATTAATTATGAA | 2074 |
rs753781937 | snp | C/T | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516595 | CAGAGCTAGTCAAGC[C/T]AAGATGTACACCTTT | 2074 |
rs753790407 | snp | G/T | 1.71965e-05 | 0.00293222 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524769 | TGCCAAGACTGGATG[G/T]CCCCGGCTCTGAAAG | 2074 |
rs753804966 | snp | C/T | 1.65247e-05 | 0.00287438 | missense | ERCC6 | GRCh38.p7 | 10:49472994 | CCTAAGCCGCCCACC[C/T]GCGTGGTCAGAAGAA | 2074 |
rs753811607 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515557 | CCAGATAATGGCATA[C/T]CACACGTCGACGAAA | 2074 |
rs753819546 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484721 | TTCCAGGCTAGACAA[C/T]GGCGCAAGATCCTGA | 2074 |
rs753821147 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538122 | TTCATGGCCTAAGTC[C/T]TGCAGAGTATCTTCT | 2074 |
rs753828676 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508733 | AGCAATACTTCCTCA[A/T]GTGACTTGTAGCCAA | 2074 |
rs753831639 | snp | C/T | 4.94319e-05 | 0.00497127 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516674 | GTCATCAAGAAAAAG[C/T]TCAAGAATTTCTGTG | 2074 |
rs753835693 | snp | C/G | 1.67984e-05 | 0.00289809 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482675 | AAAAGTATTATCATC[C/G]TAATATTTTACCTGT | 2074 |
rs753888977 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533644 | TTGTCTCTACTAAAA[A/C]TTTAAAACCTTAGCC | 2074 |
rs753929671 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459784 | AAAAGCACAGAACAT[A/G]GGAAGTCAAAAAGGT | 2074 |
rs753938965 | snp | A/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519735 | AAGCCTCAACATCCT[A/T]ACCAACAATGCTTCC | 2074 |
rs753964609 | snp | C/G | 1.80856e-05 | 0.00300707 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515307 | TATAAAACTATGTTT[C/G]TTATCTCAGGAGGTG | 2074 |
rs753990154 | snp | C/T | | | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49471096 | TTTTAGCACTCTATT[C/T]GTCAAAAACTGCTTG | 2074 |
rs754006967 | in-del | -/A | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458583 | TATAATTAGATTGCC[-/A]AAAAAAAAAAAATCA | 2074 |
rs754014388 | in-del | -/TTACT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506530 | GGTTCACATTACTGA[-/TTACT]TAACTGGGGGAAGAG | 2074 |
rs754022718 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478344 | TTCGTTAACTCCTGG[A/G]TTTACAGACCTGTTC | 2074 |
rs754025384 | snp | A/G | | | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49483424 | CACATAGTGCCAGTC[A/G]TACCTGCTAATGTCA | 2074 |
rs754030164 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521636 | CCATCCTGTATGACA[G/T]GAAAGGGTATGAAAA | 2074 |
rs754040524 | snp | G/T | 4.94222e-05 | 0.00497078 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470291 | TTTCTTCACCAGGTG[G/T]GGAATTCGAGTTCCT | 2074 |
rs754058694 | snp | A/G | 0.00013187 | 0.00811895 | missense | ERCC6 | GRCh38.p7 | 10:49472406 | TCTTCAATGGTGCCC[A/G]CAGTCAGGAGCCTGT | 2074 |
rs754070501 | snp | C/T | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516103 | GTGCCTCTGTAAGTG[C/T]CTCACTAAACTGAAG | 2074 |
rs754072071 | snp | C/T | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517051 | TCACTATAGCACTTG[C/T]TTCTATGCTGTCATC | 2074 |
rs754076451 | in-del | -/TCTT | 4.94511e-05 | 0.00497223 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49515927 | ATAATCAAATGTGCC[-/TCTT]TCTTTTTTCTTTAAA | 2074 |
rs754115636 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533361 | TGATTTATAATATAG[C/T]GGCAAGATCAACTGT | 2074 |
rs754128408 | snp | G/T | 1.64906e-05 | 0.00287142 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524378 | TCCCAAGGTCTCCTT[G/T]CCTTTGGCAATCCCA | 2074 |
rs754146090 | snp | C/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539636 | GAGGTAGGCGGGGTT[C/T]CGAGGCAGGCGAGAA | 2074 |
rs754149250 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511585 | ATGCGCCACCATGTC[C/T]GGCTAAGTTTTGTAT | 2074 |
rs754202802 | snp | C/T | 8.26508e-05 | 0.00642795 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470935 | TATTGTATCATCTTG[C/T]GCAATTGATTACTTT | 2074 |
rs754203358 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465679 | TTGTACTAGTGAATG[A/G]GTCTTATATGAGATC | 2074 |
rs754203664 | snp | C/T | 1.79043e-05 | 0.00299196 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517160 | TAGTCCTAGTGGTAG[C/T]GGTTTTGCCTAGTGT | 2074 |
rs754224226 | in-del | -/C | 1.67801e-05 | 0.00289651 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459282 | AATTTCTAGTTTATG[-/C]CCCCCACTTCCTTCC | 2074 |
rs754233465 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | ERCC6 | GRCh38.p7 | 10:49459060 | GGGCAGAAGCTTCCT[G/T]CAGGTGCCCGCTTTC | 2074 |
rs754265680 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | ERCC6 | GRCh38.p7 | 10:49474064 | AATACTCGCTGACCC[C/T]GCTTGTGCCATATTT | 2074 |
rs754266606 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523381 | TCACCTTCCCTTTTA[C/T]GGTGCTTGCTTTATA | 2074 |
rs754282069 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49483409 | TCCTTCGTCCAAGAT[C/T]ACATAGTGCCAGTCA | 2074 |
rs754303887 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479309 | TGATAATAAAAAAGA[G/T]CTTGACCACACACAC | 2074 |
rs754332267 | snp | C/T | 0.000115937 | 0.00761283 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515389 | CAACATCACATTTTT[C/T]ACATCGAAAAGTTGT | 2074 |
rs754341082 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477456 | CCCCACCTCCACTTC[A/C]TCACCTCCAGTCACT | 2074 |
rs754356792 | snp | A/G | 1.73649e-05 | 0.00294655 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528562 | ACAGAAAACAGCAAT[A/G]AAGTGATTTATTGTT | 2074 |
rs754361376 | snp | C/T | 1.65181e-05 | 0.00287381 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517059 | GCACTTGCTTCTATG[C/T]TGTCATCTGTCTCTA | 2074 |
rs754373827 | snp | C/T | 1.67181e-05 | 0.00289115 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482902 | TTTTATTAAATTTAC[C/T]TTTTAGCAATCGCCA | 2074 |
rs754389320 | snp | C/T | 0.00013192 | 0.00812049 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515829 | ACAAGACACAGGGGA[C/T]GGATACCAGCACCAG | 2074 |
rs754429403 | snp | C/T | 1.65244e-05 | 0.00287436 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49493234 | ACAGACAATTACAGT[C/T]GGACCCAACCCCTCA | 2074 |
rs754478770 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538130 | CTAAGTCTTGCAGAG[C/T]ATCTTCTAAGGCTTA | 2074 |
rs754497059 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459705 | TTTCCTACCTTACAT[C/G]TAATGCAACTTGCCT | 2074 |
rs754498044 | snp | G/T | 1.64923e-05 | 0.00287156 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470825 | AACATCATGGTCTGC[G/T]CCAAAGGCTGGTTGA | 2074 |
rs754527970 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463355 | TCAGTGCACAAAAAG[-/T]TTTGGATTTTAGAGC | 2074 |
rs754531332 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532602 | GAGCTGGGAGGCACG[A/G]CTGGCCTCATGGATG | 2074 |
rs754533342 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520813 | ATTGTGGCATCACAC[C/T]AACCTCCAAGGCAAT | 2074 |
rs754545276 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507610 | GTTATTTACAAATTT[A/T]GTTAAATGCAATGGT | 2074 |
rs754549777 | snp | C/G | 3.29636e-05 | 0.00405964 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515756 | CTGGTTATACACTTT[C/G]ATCATGTTTGGCTGC | 2074 |
rs754552933 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462784 | AGATATCCTTTCTCA[A/C]CTATCAGATTGGGAA | 2074 |
rs754630457 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502232 | AGTTTGACTCTAGCT[A/G]TTCCATTATTACCTA | 2074 |
rs754647331 | snp | A/C/G | 4.95007e-05 | 0.00497477 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473639 | ATACACATTCCCAGT[A/C/G]AGTGCTTCTCTATTT | 2074 |
rs754653514 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470738 | TTCAGCTCCTTTAGC[C/T]TCAGATTTCTCTTCA | 2074 |
rs754709379 | snp | A/G | 4.94287e-05 | 0.00497111 | intron-variant, stop-gained | ERCC6, PGBD3 | GRCh38.p7 | 10:49516919 | CATCAGAGCCATCTT[A/G]AATAAGATACGCAGC | 2074 |
rs754737368 | snp | A/T | 1.64735e-05 | 0.00286993 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49473507 | AATCAGTGGCTGTCT[A/T]GAAGCTATTGTAGTG | 2074 |
rs754742102 | snp | C/G | 1.64741e-05 | 0.00286998 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515329 | CAGGAGGTGGTGACA[C/G]CTGCTATTCAGTGTG | 2074 |
rs754750237 | snp | G/T | 3.81105e-05 | 0.00436506 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472886 | TACTAATACATTCTT[G/T]TAAAAAAAAAATAAA | 2074 |
rs754766751 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513770 | AGGTTCCTCCCTTGA[C/G]ATATGGGGACTACAA | 2074 |
rs754775224 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527526 | CTAAAAATACAAAAA[A/C]TTAGCTGGGCATGGT | 2074 |
rs754788016 | in-del | -/ACC | 1.64885e-05 | 0.00287123 | cds-indel | ERCC6 | GRCh38.p7 | 10:49500549 | TTGCCTGTAATTTGA[-/ACC]ACGAGTCCTGATCTT | 2074 |
rs754807035 | snp | A/G | 1.65395e-05 | 0.00287567 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516549 | GAGACATAACCACTC[A/G]GAAAAATAATTCCCA | 2074 |
rs754851576 | snp | A/T | 3.31934e-05 | 0.00407377 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516401 | AAATTTGTCCACTGG[A/T]TCCAAATTTGCATTG | 2074 |
rs754858831 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526707 | TGTGGTAATTTTGCC[A/G]GAGATGAATTTCAAC | 2074 |
rs754883933 | snp | C/T | 1.68553e-05 | 0.00290299 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461321 | TAGTTGTTTGGACTC[C/T]TTGCAAGTATGGCAT | 2074 |
rs754891486 | snp | A/G | 0.000148249 | 0.00860829 | missense | ERCC6 | GRCh38.p7 | 10:49478379 | TTATCTGGCAAAGAA[A/G]GGCTCATCTTGACAT | 2074 |
rs754915569 | in-del | -/C | 1.65049e-05 | 0.00287266 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474022 | TCTGAAGTCTGTGCA[-/C]TCACCTGCCTTGACT | 2074 |
rs754962598 | snp | A/T | 1.64784e-05 | 0.00287035 | missense | ERCC6 | GRCh38.p7 | 10:49471046 | AATAGCTCATAGAGA[A/T]CATTGGATTTGAAAA | 2074 |
rs754978734 | snp | C/T | 1.67027e-05 | 0.00288982 | splice-acceptor-variant | ERCC6 | GRCh38.p7 | 10:49476312 | CGGCAAAATAAGACC[C/T]ACGGACGGGAAAAAC | 2074 |
rs755010390 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495974 | ATTAAACACCTGGAC[A/G]TGGCCTACGAGGCCA | 2074 |
rs755016115 | snp | A/C | 1.64787e-05 | 0.00287038 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524410 | TTTCCCCTGGAACTG[A/C]AAAGCCCTCTTCTGG | 2074 |
rs755032276 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503791 | TTTAGGGACAGTTAA[A/T]GATTTTTATGAATAT | 2074 |
rs755039036 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477108 | ACAAGCCCAGAGCAA[A/C]TGTGCCCATGCTCCT | 2074 |
rs755045521 | snp | A/C | 3.40617e-05 | 0.0041267 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476165 | TTCTTTTCCTCCCTC[A/C]CTTCTCTTGGTCCAC | 2074 |
rs755054032 | snp | C/T | 4.9423e-05 | 0.00497082 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524102 | TTCCGACCTCCTCCT[C/T]CTCCTTCTCCTACAG | 2074 |
rs755077879 | snp | C/T | 3.29489e-05 | 0.00405874 | missense | ERCC6 | GRCh38.p7 | 10:49532906 | TTACTGACAGGTTGA[C/T]TCTGTAAACAGTCTT | 2074 |
rs755085641 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534735 | AAAAGCAAAACGATA[A/C]CCAAAAATCAGTCTT | 2074 |
rs755108272 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521646 | TGACATGAAAGGGTA[G/T]GAAAACCAGGGAACC | 2074 |
rs755108359 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492025 | CCCTAATTTATTAAT[C/T]ATCTTATCCAGTTTA | 2074 |
rs755144269 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49524027 | TTATAATCCCCACAG[A/G]CCGACCTTAACCGCT | 2074 |
rs755146371 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459802 | AAGTCAAAAAGGTAC[C/T]AGTATTCCTAAACAT | 2074 |
rs755154783 | snp | C/G | 1.64789e-05 | 0.0028704 | missense | ERCC6 | GRCh38.p7 | 10:49459163 | GGGCCCGGATGAAGA[C/G]TCTGCATCTTCTGCT | 2074 |
rs755171192 | snp | C/T | 1.64789e-05 | 0.0028704 | missense | ERCC6 | GRCh38.p7 | 10:49470620 | CTTCTGGTCCAGATA[C/T]TGCATTTGTCTCTTC | 2074 |
rs755243867 | snp | A/C | 6.58957e-05 | 0.00573964 | missense | ERCC6 | GRCh38.p7 | 10:49459076 | CAGGTGCCCGCTTTC[A/C]CTTTCTAAACGCTCT | 2074 |
rs755264337 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502899 | GCTGGTTCATGAACT[A/G]GCTACACTAGAATAA | 2074 |
rs755267065 | snp | G/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540830 | TACTCCTGCCCCATC[G/T]AATTTTTCTGCATCA | 2074 |
rs755283741 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516832 | GAGGTTGCTGCACAG[C/T]AAACGTAGATGGAAC | 2074 |
rs755292623 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471387 | AGATCTAACACATTT[C/T]AAGAAACACCTTTTC | 2074 |
rs755318826 | snp | C/T | 2.27467e-05 | 0.00337236 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488176 | ATGCAGTGCTGTTGT[C/T]ATTAGAAGATGTCTG | 2074 |
rs755324665 | snp | C/T | 1.65136e-05 | 0.00287342 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49505967 | AGAATCGTCCTCCAG[C/T]TTCAGACGTTTCTCT | 2074 |
rs755346208 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511610 | TTGTATTTTTTGGTG[C/T]AGATGGGGTTTTGCC | 2074 |
rs755363678 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529105 | ACTCCTCTTTGTCTT[A/G]TTCCCTTCCACATCA | 2074 |
rs755377100 | snp | A/G | 6.59e-05 | 0.00573983 | missense | ERCC6 | GRCh38.p7 | 10:49470272 | CTTGCTTCTGGTAAC[A/G]CCTTTTCTTCACCAG | 2074 |
rs755390240 | snp | G/T | 1.65274e-05 | 0.00287462 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528400 | GAACACAGAGAAACT[G/T]CTCCTAGCATCCTCA | 2074 |
rs755395023 | snp | C/T | 1.64985e-05 | 0.0028721 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482714 | AGCATTTGAATATCC[C/T]CCCATGGTGATGGGG | 2074 |
rs755398816 | snp | G/T | 1.656e-05 | 0.00287745 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524797 | AAGAACAATAGCAAT[G/T]CGTTTCGCACTAGCA | 2074 |
rs755411990 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477827 | TCTGCTCAGGTGTCA[G/T]TTCATCAAAGGTCTT | 2074 |
rs755423778 | snp | G/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539793 | CTCAGCTCAGGATCG[G/T]TGCTAGGAGAAGGTG | 2074 |
rs755440710 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510760 | TAGGGAAAAGGAAGA[C/T]ACAGACAGAGAAGCG | 2074 |
rs755469896 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523477 | AAAGGTATGCTGTGC[A/G]TACAAAGTACACTTT | 2074 |
rs755479389 | snp | C/T | 3.66052e-05 | 0.004278 | missense | ERCC6 | GRCh38.p7 | 10:49461539 | TGGCATCGTGCTTCA[C/T]GACACTGTGCACGCC | 2074 |
rs755509828 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465764 | CATGAAAGATGTTAC[G/T]TGCTCCTCCTTGCAT | 2074 |
rs755534739 | in-del | -/A | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521444 | AGCTCCCAGGCCCAC[-/A]AATGTGCAAAGCAGT | 2074 |
rs755554536 | snp | A/C/T | 3.29469e-05 | 0.00405864 | missense | ERCC6 | GRCh38.p7 | 10:49478409 | TCTGACTTCATTCTC[A/C/T]GCAGTAGGTATGGAT | 2074 |
rs755600403 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478182 | AGAGGGAGGTCAAAG[C/G]CTGTGGACTAGAGAA | 2074 |
rs755609247 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473267 | GCTGTAGAAAACGCA[C/T]TCTTTGTTTGAACAT | 2074 |
rs755640583 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49505831 | TCCTAAAATGTTAAT[G/T]TGTACATAATGGCTT | 2074 |
rs755663107 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524444 | TTCTTGATGTGCTTT[C/T]TCAAACGCTCCTCTT | 2074 |
rs755673576 | snp | A/C | 1.64993e-05 | 0.00287218 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500531 | CAGTCTGCAGAGGAG[A/C]ACTTGCCTGTAATTT | 2074 |
rs755694591 | in-del | -/A | 5.12378e-05 | 0.00506125 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532986 | AGACTACCTAAAAGG[-/A]AAAAAAATTTATAAG | 2074 |
rs755721992 | snp | C/T | 3.29457e-05 | 0.00405854 | missense | ERCC6 | GRCh38.p7 | 10:49532706 | GCTCAAGGGCCTGGG[C/T]GCTAGGCTCTACTGC | 2074 |
rs755725628 | snp | A/G | 3.30349e-05 | 0.00406403 | missense | ERCC6 | GRCh38.p7 | 10:49461428 | CTGCTCCCAGACACC[A/G]CTGACGAGAGAGCCT | 2074 |
rs755737597 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464359 | TTCAACAGGTGACAT[-/G]GGTGTTGTTAAAGGC | 2074 |
rs755792401 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455308 | AATCAGAAACATTAT[A/G]TTAATTATAAAGAGG | 2074 |
rs755815763 | snp | C/T | 6.70286e-05 | 0.00578877 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461331 | GACTCCTTGCAAGTA[C/T]GGCATGCAGCAATCT | 2074 |
rs755833021 | snp | C/G | 1.64874e-05 | 0.00287113 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515851 | CAGCACCAGATGAGG[C/G]AACAGTGACAACACT | 2074 |
rs755833828 | snp | C/G | 1.65026e-05 | 0.00287246 | missense | ERCC6 | GRCh38.p7 | 10:49470839 | CTCCAAAGGCTGGTT[C/G]AATCCTTCTTTTTAG | 2074 |
rs755847436 | in-del | -/AT | 4.9423e-05 | 0.00497082 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473470 | CCCTGTTACATTCAC[-/AT]GTTACCTCATTGTAT | 2074 |
rs755854972 | snp | C/T | 0.000181215 | 0.00951706 | missense | ERCC6 | GRCh38.p7 | 10:49459086 | CTTTCACTTTCTAAA[C/T]GCTCTGGCAGAATCA | 2074 |
rs755899444 | snp | C/T | 1.64996e-05 | 0.0028722 | missense | ERCC6 | GRCh38.p7 | 10:49470493 | CTGGGTCTTTCTCTT[C/T]TGTAAGAAAGACCTA | 2074 |
rs755905226 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | ERCC6 | GRCh38.p7 | 10:49530800 | GAGGGCTAAGCTGTT[C/T]AATAATTTTATTGAT | 2074 |
rs755918342 | snp | A/C | 6.59141e-05 | 0.00574045 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515533 | GTTCTGGAGGATGAC[A/C]ATGGGTCTCCAGATA | 2074 |
rs755918437 | snp | A/G | 1.64757e-05 | 0.00287012 | stop-gained | ERCC6 | GRCh38.p7 | 10:49483453 | CATCCTGCATCAATC[A/G]AATGTAGGAGTAAGA | 2074 |
rs755929758 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525077 | ATAAATACAGTTATA[A/G]ATAGTCAAGTTTAGC | 2074 |
rs755950704 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526094 | TTTTATTTATATTTA[C/T]ATATTTATATATTTA | 2074 |
rs755956674 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511059 | CATCATTTTGAACAA[C/T]AAAAAGGTAAATAAA | 2074 |
rs755965783 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537973 | GTGATCCACCCACCT[C/T]GGCCTCCCAACAACG | 2074 |
rs755974092 | in-del | -/AGATGGCATTTGG | 3.30224e-05 | 0.00406326 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49470853 | TGAATCCTTCTTTTT[-/AGATGGCATTTGG]GTGTCTGAACATCTG | 2074 |
rs755981169 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463446 | AGGAGGAATAGCTCT[C/T]TGTTAATTAATACTG | 2074 |
rs755984320 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536356 | ATGGCTGGAGGGAGA[C/G]AGAGGAGATAACCCA | 2074 |
rs756004338 | snp | C/T | 6.59261e-05 | 0.00574097 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515429 | ACATTCAGCGCATCG[C/T]GTTTGCTTTCCCTGT | 2074 |
rs756023188 | snp | C/T | 1.6516e-05 | 0.00287362 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472990 | GACACCTAAGCCGCC[C/T]ACCCGCGTGGTCAGA | 2074 |
rs756056646 | snp | A/G | 1.65359e-05 | 0.00287536 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516571 | TAATTCCCAGAAAAC[A/G]TTTGAATTCAGAGCT | 2074 |
rs756108342 | snp | G/T | 1.64746e-05 | 0.00287002 | missense | ERCC6 | GRCh38.p7 | 10:49470211 | AGCTTTTCCAAAACA[G/T]AATCGTCATTGCTCT | 2074 |
rs756126597 | snp | A/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458630 | CTTTAGCTAGCATTA[A/T]TAAAACTTTTAACTT | 2074 |
rs756131467 | snp | C/T | 1.65116e-05 | 0.00287324 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49505982 | CTTCAGACGTTTCTC[C/T]TTGTCCTGCAGTCTC | 2074 |
rs756151220 | snp | C/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517493 | CTTGGCAATGACCTT[C/G]AGCAGTAGGGCATGA | 2074 |
rs756159216 | snp | A/G | 1.64931e-05 | 0.00287163 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515976 | AGTGGAACTCTGTCA[A/G]TGTGATCCTTTCTCA | 2074 |
rs756184371 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499566 | TTCCTGGGCACACCC[C/T]TCTAGCAACTACCTT | 2074 |
rs756186917 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462399 | TAAAAAGCAAAACCA[C/T]ACAAGTAGTACAAGA | 2074 |
rs756223998 | snp | A/C | 1.64846e-05 | 0.0028709 | missense | ERCC6 | GRCh38.p7 | 10:49472404 | TTTCTTCAATGGTGC[A/C]CGCAGTCAGGAGCCT | 2074 |
rs756278990 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501984 | AATAAAAAGATGATG[C/T]AAGATAAGGCATTTT | 2074 |
rs756320234 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457285 | TGGCAAAGTGACAAA[A/G]ATAATGTAATCATCT | 2074 |
rs756377912 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478008 | AAATGTGAGTCCCCA[C/T]GAGAACAAAACTTGC | 2074 |
rs756385124 | snp | A/C | 1.65293e-05 | 0.00287479 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472332 | AATTCCCTGCTCAAG[A/C]CTCTGGGAACGCACA | 2074 |
rs756392659 | snp | A/G | 1.65718e-05 | 0.00287848 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473981 | TGTGAGTTGATGGCT[A/G]TCATAAAGAACCAGC | 2074 |
rs756425090 | snp | G/T | 4.94482e-05 | 0.00497209 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515765 | CACTTTGATCATGTT[G/T]GGCTGCTGAACTTGT | 2074 |
rs756444847 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464866 | AACTCCTAGATGCCC[A/G]GGCAGAAGTTTGCTG | 2074 |
rs756458574 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510536 | GGCCCTCCCAATCCC[A/G]TGACATCTTGGACAC | 2074 |
rs756468509 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499724 | TTTACAGTTTAAATA[C/T]GGAAGTGCTCATAGT | 2074 |
rs756476559 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509301 | CATACATTTTCTGAA[A/G]TCCTCACGACAACCC | 2074 |
rs756484672 | snp | C/T | 4.94238e-05 | 0.00497086 | missense | ERCC6 | GRCh38.p7 | 10:49458942 | TTGGATTCAAACTCC[C/T]GCAGTATCTCCCTGG | 2074 |
rs756519991 | snp | A/G | | | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49538967 | GAACACTCACCCAGG[A/G]CCGCGCGAGCGCCCA | 2074 |
rs756549029 | snp | C/T | 1.72761e-05 | 0.002939 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528558 | GAAGACAGAAAACAG[C/T]AATGAAGTGATTTAT | 2074 |
rs756554187 | snp | A/C | 1.66502e-05 | 0.00288527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482895 | AGCACCTTTTTATTA[A/C]ATTTACCTTTTAGCA | 2074 |
rs756554927 | snp | A/G | 1.6476e-05 | 0.00287014 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516930 | TCTTGAATAAGATAC[A/G]CAGCTGTGTGCAACA | 2074 |
rs756556460 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501773 | CCAGCATGGGCAACA[C/T]AGTAAGACCTCATCT | 2074 |
rs756558437 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471436 | CATAGTCTCTCTTAG[A/C]CTCCTTGACTTGAAT | 2074 |
rs756564516 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521075 | TAGGTCCTATTTGTG[C/T]CCAAGTCTATTAACA | 2074 |
rs756594350 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533453 | TAGGCTGAATACCTA[C/T]CCAGTAAATAGGAGC | 2074 |
rs756622786 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | ERCC6 | GRCh38.p7 | 10:49473536 | TGGTACCATCCATCT[C/T]GAGATAGGTATACTT | 2074 |
rs756639495 | snp | C/T | 3.31829e-05 | 0.00407313 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458777 | ATCAGAAATGCCCGT[C/T]AGAAAAAGGGACTTG | 2074 |
rs756648642 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474617 | TCCTATCAACCTAAA[-/T]TTGGAGACATCAGTC | 2074 |
rs756662155 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470288 | CCTTTTCTTCACCAG[A/G]TGTGGAATTCGAGTT | 2074 |
rs756678342 | snp | C/T | 1.65908e-05 | 0.00288012 | missense | ERCC6 | GRCh38.p7 | 10:49482688 | TCCTAATATTTTACC[C/T]GTACTGGGGAAGCAT | 2074 |
rs756678950 | snp | A/G | 3.62207e-05 | 0.00425547 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515301 | ATAATGTATAAAACT[A/G]TGTTTCTTATCTCAG | 2074 |
rs756687999 | in-del | -/CAGA | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457526 | AGTCACATGGATGAG[-/CAGA]CAGAAGATCTGGACA | 2074 |
rs756713165 | snp | C/T | 4.94368e-05 | 0.00497152 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482819 | CTCTCGGAGGTTATT[C/T]TGCATCGGTGAGCCA | 2074 |
rs756723239 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485397 | AGTTTAAAAAGAAGA[C/T]TGTATGTGATATACA | 2074 |
rs756736539 | in-del | -/AG | 1.64754e-05 | 0.00287009 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49532916 | GTTGACTCTGTAAAC[-/AG]TCTTGCTCCTGAGTT | 2074 |
rs756737104 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490242 | TTAACAAAGATAACA[C/T]AGGATCAAAGGGTGA | 2074 |
rs756743738 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484204 | GAGGATCCCTTGAGC[C/T]CAGGAGGTCAAGGCT | 2074 |
rs756760457 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524650 | AAGCATGATTTTTCT[A/G]GGCTTTTTCTCCTGT | 2074 |
rs756763474 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471923 | TGGAAAGACAGAGGA[C/T]GAAACAGCCATCCTG | 2074 |
rs756769019 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517496 | GGCAATGACCTTGAG[C/T]AGTAGGGCATGAATA | 2074 |
rs756817906 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498756 | AGAGAGCATGTTTTA[A/G]TTTTTAGATCAAAAC | 2074 |
rs756818804 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478741 | GATAATTTTGTGCCT[G/T]ATTTCTCTTATACAC | 2074 |
rs756881696 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532869 | ACCACCACTTTCTTG[C/T]TTGATTGCCATTTCT | 2074 |
rs756881893 | in-del | -/CTT | 3.29481e-05 | 0.00405869 | intron-variant, cds-indel | ERCC6, PGBD3 | GRCh38.p7 | 10:49516976 | TATTTATTGTTCCAC[-/CTT]CTTCATCTCCTGATT | 2074 |
rs756908657 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481318 | TTCTGTTAAGTTTGA[A/G]ATTATTTCAAAATAA | 2074 |
rs756910210 | snp | C/T | 1.64953e-05 | 0.00287182 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478503 | AAGGGAACATTACTA[C/T]ATATGTTTAAGGAAC | 2074 |
rs756924709 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | ERCC6 | GRCh38.p7 | 10:49539533 | CCCTCCGCCACGCGC[A/G]CACCTGGGCGGAGTG | 2074 |
rs756924830 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479194 | AATTATTGCTACTTC[-/A]AAAAAAAATCTAAAT | 2074 |
rs756927412 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465637 | GAGGTGACTGAATTA[C/T]GGGGTTGGGTCTTTC | 2074 |
rs756951136 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | ERCC6 | GRCh38.p7 | 10:49471017 | TCTGGGATGCATCAG[A/G]ACTAGTCAGAGTAAA | 2074 |
rs757008329 | snp | A/G | 0.000181613 | 0.0095275 | missense | ERCC6 | GRCh38.p7 | 10:49493125 | GTGTTACCTTTTTGT[A/G]GGTATAGGAACCGGT | 2074 |
rs757014778 | in-del | -/CTCT | | | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49515093 | AAAGAAGGCAATGTG[-/CTCT]CTAAGAAAACATCTT | 2074 |
rs757017310 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49505450 | GTACAATATAAGACA[A/C]TCAAAAAAAATGTCA | 2074 |
rs757023567 | snp | A/G | 2.41502e-05 | 0.00347484 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488199 | GATGTCTGTGAAAGG[A/G]CTGCTGTTATTATGG | 2074 |
rs757036326 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462811 | GAAAAATTAAAAGTG[-/T]TAACACCACACTCTT | 2074 |
rs757037155 | snp | C/T | 1.65031e-05 | 0.00287251 | missense | ERCC6 | GRCh38.p7 | 10:49500647 | CCAGAATTCCTCCTG[C/T]CTGCTGGCAGTGCAA | 2074 |
rs757042401 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49493320 | TCAACTGCTCAAAAG[A/T]TCCCCCAAAACAACA | 2074 |
rs757069702 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462179 | GAGGAAAGAAGAGAC[A/G]CAACAGGAGATTGAC | 2074 |
rs757070594 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534873 | CCAGCAATAAAGCAC[C/T]GGGATACAAAGAATT | 2074 |
rs757080596 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465179 | CTTGCATCAGCGTGA[A/C]CTGGATGCGAGACAA | 2074 |
rs757085830 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511011 | TTAGAATCTTATAAC[-/A]AAAAAAAAAAAAAGA | 2074 |
rs757094712 | snp | A/T | 1.64762e-05 | 0.00287016 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515657 | GAAACAGAACAAAAG[A/T]GGGCTTGAATACCAT | 2074 |
rs757100986 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534066 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGA | 2074 |
rs757101424 | snp | A/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518476 | GATTAAACGAATTAA[A/C]CTATATAACAAGAAG | 2074 |
rs757148460 | snp | A/G | 4.96134e-05 | 0.00498039 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473054 | GACACACAACACTGA[A/G]CACACACACTTAAGA | 2074 |
rs757179093 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515561 | ATAATGGCATACCAC[A/G]CGTCGACGAAACTCC | 2074 |
rs757209271 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464904 | AGGGTTCTCATGGAG[-/A]ATCTCTCCTAGGGCA | 2074 |
rs757218885 | snp | G/T | | | missense | ERCC6 | GRCh38.p7 | 10:49461529 | CCATCCATGATGGCA[G/T]CGTGCTTCATGACAC | 2074 |
rs757222408 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516772 | TTAGGTCGGCTTTTT[C/T]CCATTTGCAAAGAAT | 2074 |
rs757228005 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468367 | GTTCTCCCTCTTTCT[A/G]TTACAGCACGAAAAT | 2074 |
rs757279099 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500345 | CATTAAAAGTGTTAC[A/T]TGTTTAATTTCTCCT | 2074 |
rs757294747 | snp | A/G | 3.30803e-05 | 0.00406682 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515392 | CATCACATTTTTCAC[A/G]TCGAAAAGTTGTGTT | 2074 |
rs757301777 | snp | C/G | 1.80055e-05 | 0.00300041 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515314 | CTATGTTTCTTATCT[C/G]AGGAGGTGGTGACAC | 2074 |
rs757308596 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506495 | CATAAAGCAAATTTG[C/G]GGTCAAAATCACTGA | 2074 |
rs757326868 | in-del | -/CCGTCAGGTTGACACCTAAGCCGCCCACCCGCGTGGTCAGAAGAAA | 1.65302e-05 | 0.00287486 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49472965 | CAACTCTGTTTGCCC[lengthTooLong]CACAAATATGGATGT | 2074 |
rs757358097 | snp | A/G | 1.75526e-05 | 0.00296243 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528567 | AAACAGCAATGAAGT[A/G]ATTTATTGTTAAATA | 2074 |
rs757369362 | snp | C/T | 0.000164728 | 0.00907398 | missense | ERCC6 | GRCh38.p7 | 10:49470370 | GGTCTCAGATGTTTC[C/T]CCAGGGTCTCTTCTT | 2074 |
rs757426652 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513104 | ATAGCTAATACTTAC[A/G]GAGTGCCTGATGTAT | 2074 |
rs757487575 | in-del | -/ATTCT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506829 | AAAAAAAAGCCTCAA[-/ATTCT]ATTCACTTTCAAAAT | 2074 |
rs757516474 | snp | C/T | 8.91083e-05 | 0.00667429 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524803 | AATAGCAATGCGTTT[C/T]GCACTAGCATGAAAC | 2074 |
rs757524911 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494340 | CATATAGAAAATACT[A/G]TAAGATTCTGTTAAA | 2074 |
rs757525603 | snp | A/C | 3.32276e-05 | 0.00407586 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472522 | CTTCCCAATGACAAG[A/C]ACTGACTATAAGAAA | 2074 |
rs757526020 | snp | A/G | 3.30584e-05 | 0.00406548 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470936 | ATTGTATCATCTTGT[A/G]CAATTGATTACTTTA | 2074 |
rs757528340 | in-del | -/TT | 1.64887e-05 | 0.00287125 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49470433 | TGCTTATAAAAATTA[-/TT]TTCCATTTGTTTATT | 2074 |
rs757548593 | snp | A/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520941 | ATTGTTAATTTGGAT[A/T]AGGGTCATATTAATA | 2074 |
rs757553499 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475957 | AGTAACTGCACAGCT[C/T]GCAGCTGCATTTGCG | 2074 |
rs757591171 | snp | A/G | 1.7913e-05 | 0.00299268 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517161 | AGTCCTAGTGGTAGT[A/G]GTTTTGCCTAGTGTT | 2074 |
rs757621118 | in-del | -/TGTC | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526427 | TCGCCCATTTTTGTT[-/TGTC]TGTTTCTTTAAATGA | 2074 |
rs757622548 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456223 | AAGACTGGCAGGCCA[A/G]CTTCTCCTTCCTCAA | 2074 |
rs757624794 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49532275 | TTTGTGCACATGCTG[A/G]TGAACAGCCCTTCTC | 2074 |
rs757647051 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519938 | GAGCCCAGGCCCCTA[C/T]CCTCTGAAGGTGTTT | 2074 |
rs757665118 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489167 | AGAATAAAAGGTCTA[G/T]ATGATCTTGAATGAC | 2074 |
rs757707707 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456867 | GTGTCAGATCTCCAC[A/G]CTGAGACACCACCTT | 2074 |
rs757725557 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515860 | ATGAGGCAACAGTGA[C/T]AACACTGTTATCATT | 2074 |
rs757727257 | snp | C/G | 1.64795e-05 | 0.00287045 | missense | ERCC6 | GRCh38.p7 | 10:49474072 | CTGACCCTGCTTGTG[C/G]CATATTTTCAACAAA | 2074 |
rs757732685 | snp | C/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458446 | GACCTGTTTTTAGCA[C/G]CAATAAAAAAAAATA | 2074 |
rs757794095 | snp | G/T | 1.64735e-05 | 0.00286993 | missense | ERCC6 | GRCh38.p7 | 10:49458977 | GGCCTGGCCATCAGT[G/T]TGGGCCTGGAAAGCG | 2074 |
rs757810107 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49473499 | TATCTCGTAATCAGT[A/G]GCTGTCTTGAAGCTA | 2074 |
rs757815168 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49483415 | GTCCAAGATCACATA[A/G]TGCCAGTCATACCTG | 2074 |
rs757828668 | snp | C/T | 1.65419e-05 | 0.00287588 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49517073 | GCTGTCATCTGTCTC[C/T]AAAAGGTCAGTTATT | 2074 |
rs757845558 | snp | A/C | 3.29549e-05 | 0.00405911 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515669 | AAGAGGGCTTGAATA[A/C]CATTTCTTTCCACGG | 2074 |
rs757873730 | snp | C/G/T | 6.59125e-05 | 0.00574045 | missense | ERCC6 | GRCh38.p7 | 10:49470646 | TCTTCTCCAAGCCTA[C/G/T]CATTGCTAGTTACAT | 2074 |
rs757880779 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501913 | TGCAATGAACCATGA[C/T]TGCACCACCGGATTC | 2074 |
rs757911809 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49482621 | GACTTGGCTACAAAT[C/T]ATAGTATTTAATAGG | 2074 |
rs757913740 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497361 | AAATATTTTTACAAC[A/G]AACTCACATTCAAAT | 2074 |
rs757921877 | in-del | -/A | 3.33834e-05 | 0.00408541 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505839 | TGTTAATTTGTACAT[-/A]ATGGCTTGATAGCAA | 2074 |
rs757947659 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510365 | CCATGTATGCAGCCT[C/T]CTCATCTCTGTGCAC | 2074 |
rs757954437 | snp | A/T | 1.65386e-05 | 0.00287559 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532519 | TACCACCACTTTGAA[A/T]GGAAGAAGATGGGCT | 2074 |
rs757994191 | in-del | -/GTAGCTATTAACCCTAGACAAT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527144 | CTTGGATTTGAGGAG[-/GTAGCTATTAACCCTAGACAAT]GTAGCTATTAACCCT | 2074 |
rs758001816 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496103 | TCCCTTCCTCCAATC[A/G]ACCTTCACCATGTCC | 2074 |
rs758026454 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509041 | GAAGTGCAGGCCCAG[A/G]CACAAAAGTCTGAGC | 2074 |
rs758092872 | snp | A/T | 3.29544e-05 | 0.00405908 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516712 | TCATTACGGTGAAGA[A/T]ATCGTTTGGTGGTGC | 2074 |
rs758107523 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463779 | GAGTTTTCCTGCATA[A/G]GCTCTCTTTGCCTGC | 2074 |
rs758110633 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460161 | CAGAAATGCTGCTAC[A/G]GATCTTGGGTTAAAG | 2074 |
rs758120957 | snp | C/T | 5.26025e-05 | 0.00512821 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524790 | GCTCTGAAAGAACAA[C/T]AGCAATGCGTTTCGC | 2074 |
rs758161786 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471629 | CTCCACCAGCCACCC[C/T]GTCCCTCCCTGTCAT | 2074 |
rs758168100 | snp | C/G | 1.65302e-05 | 0.00287486 | missense | ERCC6 | GRCh38.p7 | 10:49476291 | TTATGCTGCTCATCT[C/G]TAAGACGGCAAAATA | 2074 |
rs758183204 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503965 | GTTTGTCATTTGACT[G/T]CTAAATTAGATAGAC | 2074 |
rs758184943 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488787 | GTTTTTGTGTTATTT[A/G]CTTTTTTTCTTTTTG | 2074 |
rs758195013 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471285 | TCAGGAAATATATAA[-/T]ACATCAGTTAATCTC | 2074 |
rs758196824 | snp | G/T | 1.6577e-05 | 0.00287893 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516292 | GACGACCAAAATAAG[G/T]AACCATGAATTCATC | 2074 |
rs758238639 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534028 | AATCCCAGCCACTCG[G/T]GAGGCTGAAGCAGGA | 2074 |
rs758249800 | snp | G/T | 1.69301e-05 | 0.00290942 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461305 | ATTTTATTTCTAGCC[G/T]TAGTTGTTTGGACTC | 2074 |
rs758257014 | snp | C/G/T | 8.23993e-05 | 0.00641823 | missense, synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524395 | CTTTGGCAATCCCAC[C/G/T]TTCCCCTGGAACTGC | 2074 |
rs758268075 | snp | C/G | 1.64765e-05 | 0.00287019 | missense | ERCC6 | GRCh38.p7 | 10:49470727 | ACTGCATTTACTTCA[C/G]CTCCTTTAGCCTCAG | 2074 |
rs758275606 | snp | C/G | 1.65499e-05 | 0.00287657 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524263 | GTCCGCCTCTGCCCC[C/G]TCCACCTCGTCATCT | 2074 |
rs758317802 | snp | C/T | 1.68303e-05 | 0.00290084 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460333 | CAGCATTCAATCAAG[C/T]AAGTCTCACCCTGGA | 2074 |
rs758331556 | snp | G/T | 1.65042e-05 | 0.0028726 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49493210 | CCACTGATGCATCAC[G/T]GTTGTTGGACAGACA | 2074 |
rs758341467 | in-del | -/TT | 1.6475e-05 | 0.00287006 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49470244 | TCCTTGGCCTCACTC[-/TT]GTTTTCACTGTCTTG | 2074 |
rs758360895 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462255 | GATAAAGGCATCTCT[A/C]ATCACTGAGAAAAAC | 2074 |
rs758395933 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515736 | CTGTCTACGCCTCCC[A/G]TGAACTGGTTATACA | 2074 |
rs758397318 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511680 | ATCTGCCTGCCTTGC[C/T]TTCCAAAGTGCTAGG | 2074 |
rs758404624 | in-del | -/AGAAAGGTACAC | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485619 | ACCCTGTCCAATGGT[-/AGAAAGGTACAC]AGGCAATAGATATTT | 2074 |
rs758410428 | snp | C/G | 1.64789e-05 | 0.0028704 | missense | ERCC6 | GRCh38.p7 | 10:49474092 | TTTTCAACAAAGACT[C/G]AACAACAATCATTTT | 2074 |
rs758411255 | snp | C/T | 1.66032e-05 | 0.0028812 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517090 | AAAGGTCAGTTATTT[C/T]ATGTAAACTTAGTGT | 2074 |
rs758425348 | in-del | -/AAT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479466 | ATAGGCTTTACTTTG[-/AAT]AATACATAAAAAAGA | 2074 |
rs758433804 | snp | A/C | 1.64754e-05 | 0.00287009 | missense | ERCC6 | GRCh38.p7 | 10:49483438 | CATACCTGCTAATGT[A/C]ATCCTGCATCAATCG | 2074 |
rs758439687 | in-del | -/C | 1.6478e-05 | 0.00287032 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49516651 | TGACAATGAGTTCAA[-/C]TGACCTCGTCATCAA | 2074 |
rs758440768 | snp | C/T | 4.53957e-05 | 0.00476401 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488162 | GCCTGACTTACTGAA[C/T]GCAGTGCTGTTGTCA | 2074 |
rs758479814 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | ERCC6 | GRCh38.p7 | 10:49530782 | CTCTGCTGGTGGCAG[C/T]TTGAGGGCTAAGCTG | 2074 |
rs758490857 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49466365 | ACAAGTAACTCAGTA[A/C]GTTGTGAATGAAGGT | 2074 |
rs758532582 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478293 | GCAGAGGAGAATCAG[A/C]GTGAAGGGAAAGACA | 2074 |
rs758560323 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523505 | TTTTTGCATGATGGT[A/G]GCTTATAATTATGCA | 2074 |
rs758573063 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530692 | TGACTTTTTCAAAAA[C/T]GCAATACTGAATGTT | 2074 |
rs758587727 | snp | A/G | 0.000115311 | 0.00759224 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459070 | TTCCTGCAGGTGCCC[A/G]CTTTCACTTTCTAAA | 2074 |
rs758647483 | snp | C/T | 1.64743e-05 | 0.00287 | missense | ERCC6 | GRCh38.p7 | 10:49470382 | TTCTCCAGGGTCTCT[C/T]CTTCTGCCACACTAT | 2074 |
rs758672826 | in-del | -/G | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539251 | CGCTGCCGGTCAGCT[-/G]GGTGGCTTGCGAAGG | 2074 |
rs758679804 | snp | A/T | 0.000131783 | 0.00811628 | missense | ERCC6 | GRCh38.p7 | 10:49458988 | CAGTGTGGGCCTGGA[A/T]AGCGATGAAGTTTCT | 2074 |
rs758688919 | snp | A/T | 1.65299e-05 | 0.00287483 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524682 | TCTGAGGGATCTGGG[A/T]ACCAAAAGGTGTCAT | 2074 |
rs758694670 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492157 | GATTTTTCTGAGTCA[C/T]TTCTATCAAAAGTTT | 2074 |
rs758695425 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487746 | TGCTTAAGGATTGAA[A/G]TTTATCTGGAAAATT | 2074 |
rs758707340 | snp | C/T | 0.000280045 | 0.0118298 | missense | ERCC6 | GRCh38.p7 | 10:49532889 | TTGCCATTTCTTCAT[C/T]ATTACTGACAGGTTG | 2074 |
rs758711210 | snp | C/T | 3.33023e-05 | 0.00408044 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516133 | GGACAAGTGACGCAC[C/T]GACACCATATTCCTC | 2074 |
rs758810393 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456559 | CAAACCTAGGGCTGT[A/G]CTTAGCTGTGGAACA | 2074 |
rs758815631 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507674 | GTCCCTTCAACCCCA[-/C]CCTGGGGTAATCTGA | 2074 |
rs758842874 | snp | C/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540937 | TACAATTGGCTTCTA[C/T]GGCCTAGCAAGCATA | 2074 |
rs758853358 | snp | C/T | 1.65149e-05 | 0.00287353 | stop-gained | ERCC6 | GRCh38.p7 | 10:49500667 | TGGCAGTGCAATTCC[C/T]ACAGCCACCTAACAC | 2074 |
rs758866625 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499253 | CCAAGTGTTTTCTTC[C/T]CCTTCCTACATCTAT | 2074 |
rs758874692 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525997 | TTTGTTAACTCTCAC[C/T]GTTAATGCACATTTG | 2074 |
rs758877704 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49471036 | AGTCAGAGTAAATAG[C/T]TCATAGAGATCATTG | 2074 |
rs758928784 | snp | A/C | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455598 | CATGTGATGAGTTGA[A/C]AGCTGACATTTTAAA | 2074 |
rs758946423 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468214 | GTGCCAGTGGAGACT[C/G]TGCAGACCTGTGGGG | 2074 |
rs758984257 | snp | C/T | 3.30715e-05 | 0.00406628 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516016 | TTGCCTGATGTCCCA[C/T]TGAACTGAGCTTATC | 2074 |
rs758986305 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512900 | CAGATTTTGGATTTT[C/T]GGACTAGGGATGGTC | 2074 |
rs759016000 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494654 | ATCTATAACCTGTCA[A/G]TGCATGGTACTCCCC | 2074 |
rs759021405 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485355 | GACACTAGGCTACAC[C/T]ACCTCCTACTAAAAT | 2074 |
rs759031177 | snp | A/G | 3.45095e-05 | 0.00415374 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517129 | TCTTGGGACTAAAAC[A/G]GAAAAAAGGTATTAT | 2074 |
rs759036621 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467343 | ATTCCCACCAGGCGT[A/G]TATGAGACCCAACTG | 2074 |
rs759068837 | snp | A/G | 1.64885e-05 | 0.00287123 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474042 | CTGCCTTGACTGAGA[A/G]AACAGCAATACTCGC | 2074 |
rs759080988 | snp | C/G | 1.64741e-05 | 0.00286998 | missense | ERCC6 | GRCh38.p7 | 10:49483371 | GCAAGGGTGACAGCA[C/G]CATTTGGATTTCGAA | 2074 |
rs759104524 | snp | A/G | 0.000115305 | 0.00759205 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459025 | CACCAGAAGGTCATC[A/G]TGTTCTGTGGTGGGC | 2074 |
rs759122499 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49493063 | GAGAAAAACCAAATA[A/T]GTAAAATGGAGGGCA | 2074 |
rs759125039 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | ERCC6 | GRCh38.p7 | 10:49458906 | AGTTCTCGGAAGACA[C/G]AAGACTGTGATGCAG | 2074 |
rs759170995 | snp | C/T | 1.68354e-05 | 0.00290128 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515367 | ACGGAACACTTCACA[C/T]GTAAGGCAACATCAC | 2074 |
rs759192051 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49532117 | GCAAATCTGAAAAAT[C/T]GCCCAAGGACTGAAC | 2074 |
rs759204996 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459463 | ATAAAGAGGGGGCAA[C/G]CAAGCCATTCCCTTA | 2074 |
rs759208753 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470351 | GTTCTTAGGCTTTTG[C/T]TTTGGTCTCAGATGT | 2074 |
rs759238503 | snp | A/T | 1.64735e-05 | 0.00286993 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524625 | ACTTTTCGAAGCCTG[A/T]TGCTTCATTAAGCAT | 2074 |
rs759252862 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | ERCC6 | GRCh38.p7 | 10:49532849 | TACTCCTCCACCTCC[C/T]CATCACCACCACTTT | 2074 |
rs759288294 | snp | G/T | 1.67326e-05 | 0.00289241 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500743 | AAATGGCAAATGGTG[G/T]ATAATACAGATCATA | 2074 |
rs759288321 | snp | C/T | 3.29587e-05 | 0.00405934 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478477 | AGTTTTGACCTTTAA[C/T]AAGAGCAGAGAAGGG | 2074 |
rs759289532 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502474 | CCAACTGCTGAGGAG[A/G]CACCAGGCCAGGTGG | 2074 |
rs759300101 | snp | A/C | 1.66538e-05 | 0.00288559 | missense | ERCC6 | GRCh38.p7 | 10:49461469 | AGGGCATCCTGGGCC[A/C]CTCGGTTGGCTTCTG | 2074 |
rs759307809 | in-del | -/T | 1.64958e-05 | 0.00287187 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49515981 | ACTCTGTCAATGTGA[-/T]TCCTTTCTCACTGTA | 2074 |
rs759309303 | snp | A/T | 1.69879e-05 | 0.00291439 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528545 | AATGGTAAATATAGA[A/T]GACAGAAAACAGCAA | 2074 |
rs759322509 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504144 | AATACAGTAAAAAAA[-/T]ATATCTACAGTTTAA | 2074 |
rs759325671 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458194 | TTTCCACAAATACAT[A/G]TCTTATCATTTATTA | 2074 |
rs759371690 | snp | A/T | 1.66424e-05 | 0.0028846 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516095 | TCCAGGGTGTGCCTC[A/T]GTAAGTGCCTCACTA | 2074 |
rs759378877 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473321 | CCAAATATCCAGAAG[G/T]AGGGCATAGAGTTAA | 2074 |
rs759392093 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464449 | TGATAGGAAAGAAAA[C/T]CCCATTTTCTCAAGA | 2074 |
rs759436177 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511083 | AAATAAATAAAAATT[A/G]TGTGAGTGATTTAAG | 2074 |
rs759447711 | snp | A/G | 6.59772e-05 | 0.00574319 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49500617 | GGATGGTCTTGCCCA[A/G]TCCCATTTCATCTCC | 2074 |
rs759499654 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465187 | AGCGTGACCTGGATG[C/T]GAGACAAGGAGTCAA | 2074 |
rs759507146 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518974 | ATTAAAAACCAATTA[C/T]ATCAACAGGCATCAA | 2074 |
rs759516851 | snp | A/T | 1.64746e-05 | 0.00287002 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532641 | CACCTGCTGAAGCAC[A/T]CCCTGTTCCAGCACG | 2074 |
rs759539589 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477497 | GCACCCAGAGCAAGC[C/T]TCACGGGCACCTCTG | 2074 |
rs759542213 | snp | C/G/T | 3.29616e-05 | 0.00405954 | missense | ERCC6 | GRCh38.p7 | 10:49471000 | TGCACTTGTTTCAGT[C/G/T]CTCTGGGATGCATCA | 2074 |
rs759558706 | snp | A/C | 3.30671e-05 | 0.00406602 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470907 | GTAAAGAGGAAAAAC[A/C]CCACTAATACTATAT | 2074 |
rs759569215 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | ERCC6 | GRCh38.p7 | 10:49532768 | GCTGGCCCTCTCCTC[A/G]GAGCTGCTGATGCGC | 2074 |
rs759569367 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522430 | ATGTTAAGAGCTATC[A/G]TATTTTGGTGGCAAT | 2074 |
rs759593528 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510247 | AACCCTGAAAGCTAG[C/T]TGCTGCCATTTAAAG | 2074 |
rs759596926 | snp | C/T | 1.65081e-05 | 0.00287293 | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524245 | AGTACCATCTCCAGA[C/T]AGGTCCGCCTCTGCC | 2074 |
rs759637785 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518101 | GATCCAACTGAAGGA[C/T]AGACAGGACAATCCC | 2074 |
rs759638823 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49482576 | CAGATACCAATTTAT[-/G]AGCCTGGCCATCTTT | 2074 |
rs759651537 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49472798 | CAGGAGACAATCAAA[A/C]TGTGAAACGTATGCT | 2074 |
rs759664342 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | ERCC6 | GRCh38.p7 | 10:49470781 | TCATTTACAGATATG[C/T]TAGAAGCAGGGAACT | 2074 |
rs759665340 | snp | C/T | 1.64855e-05 | 0.00287097 | missense | ERCC6 | GRCh38.p7 | 10:49532567 | TCCAGGACCGACCGA[C/T]ACTCCTTCTCCACGT | 2074 |
rs759698849 | in-del | -/CT | 1.66421e-05 | 0.00288458 | frameshift-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524317 | GGGGAAATACTCAGA[-/CT]CTTCACCCTCAGAGT | 2074 |
rs759731042 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454810 | ATACCACAATGATAA[A/G]AACAGTGGGTTACTA | 2074 |
rs759775257 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486669 | GATAGCTAAAAAGTT[C/T]GTTGCAAAAATGGAC | 2074 |
rs759776400 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525242 | CTAAAAAGGAAAAAC[A/G]TAAATGTCAGCTCTA | 2074 |
rs759797200 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517186 | AGTGTTCCAAAAATG[A/G]AACATGAAAAATGTC | 2074 |
rs759807037 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515717 | ATCAATGTTTTCATC[A/G]GCTCTGTCTACGCCT | 2074 |
rs759812880 | snp | C/T | 6.60644e-05 | 0.00574698 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493111 | GGTACTGAAATATTG[C/T]GTTACCTTTTTGTGG | 2074 |
rs759818743 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512795 | ATTTTGTGCATGAAA[C/T]GAAGTTTTGACTGTG | 2074 |
rs759831859 | snp | A/C | 1.65449e-05 | 0.00287614 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516473 | ACGTCTCATGGCAGC[A/C]CTAACCAGTACATTA | 2074 |
rs759872032 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527588 | GCTGAGGCAGGAGAA[C/T]CGCTTGAACCCGGGA | 2074 |
rs759900872 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508779 | CTGATGAGGGTCCAC[C/T]GAAGCAGCACAGCTA | 2074 |
rs759927080 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480420 | GACAGAATAAATACC[A/G]GCACACAGACTATCT | 2074 |
rs759944917 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525534 | TCCCTCTTTCATTAG[C/T]TGAAATTCATCTCTG | 2074 |
rs759947839 | snp | G/T | 1.6489e-05 | 0.00287128 | missense | ERCC6 | GRCh38.p7 | 10:49472393 | GTGGTAGATCTTTTC[G/T]TCAATGGTGCCCGCA | 2074 |
rs759974249 | in-del | -/AG | 0.00682079 | 0.0579989 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472478 | TCCCGGGCCTGCAAC[-/AG]AGAGAGAGAGACCTC | 2074 |
rs759987640 | snp | A/G | 1.65348e-05 | 0.00287526 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472498 | GAGAGAGACCTCTCA[A/G]CGAGAATCCTTCCCA | 2074 |
rs759996832 | snp | C/G | 1.65641e-05 | 0.00287781 | missense | ERCC6 | GRCh38.p7 | 10:49460425 | TGCACAGAGAAGTTA[C/G]AATTCCTTTTCTTAC | 2074 |
rs760027420 | in-del | -/T | 1.66189e-05 | 0.00288256 | splice-donor-variant | ERCC6 | GRCh38.p7 | 10:49461351 | GCAGCAATCTCTTAC[-/T]TTTTTTCCTGCTGGT | 2074 |
rs760065223 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480493 | AAGGAGCAAATACAA[A/C]CAATACTCTGCTTCC | 2074 |
rs760081870 | snp | A/G | 0.000148049 | 0.00860249 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476357 | TTCAAAAAAAAAATT[A/G]ACAGAAATAATTAAA | 2074 |
rs760082299 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535667 | CATTTTTCTATTTCT[A/G]TAAAATAATATCAAA | 2074 |
rs760084614 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479543 | TATATCATTCAGACT[A/G]ATGAATATCACCTTG | 2074 |
rs760116264 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488925 | AGTAGCTGGGACTAC[A/G]AGGTGCCTGCCACCA | 2074 |
rs760116468 | in-del | -/TACA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512009 | TTATACTTTTGAAAC[-/TACA]TAAATTTCAGATGCT | 2074 |
rs760131655 | snp | A/G | 4.98625e-05 | 0.00499287 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493265 | AACCTGCATCCAAAC[A/G]TCCAAGAAGAAAACA | 2074 |
rs760138141 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457809 | AGGATCAAAGCAACA[C/T]CATCACAGAACCACA | 2074 |
rs760146233 | snp | A/G/T | 3.29605e-05 | 0.00405948 | missense | ERCC6 | GRCh38.p7 | 10:49471010 | TCAGTGCTCTGGGAT[A/G/T]CATCAGGACTAGTCA | 2074 |
rs760171089 | snp | C/T | 4.94262e-05 | 0.00497098 | missense | ERCC6 | GRCh38.p7 | 10:49532858 | ACCTCCCCATCACCA[C/T]CACTTTCTTGCTTGA | 2074 |
rs760192995 | snp | A/T | 4.99264e-05 | 0.00499607 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516107 | CTCTGTAAGTGCCTC[A/T]CTAAACTGAAGGACA | 2074 |
rs760238086 | snp | C/T | 4.95446e-05 | 0.00497693 | missense | ERCC6 | GRCh38.p7 | 10:49474184 | AGATTCTTGGGACCT[C/T]CAGAAAAGAGATCAG | 2074 |
rs760278222 | snp | C/T | 1.68057e-05 | 0.00289872 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474281 | ACACTCAGATGACCC[C/T]ATGTAAAGTAAGATT | 2074 |
rs760280622 | snp | A/C | 1.64757e-05 | 0.00287012 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524052 | ACCGCTGCTTATAAT[A/C]ATCTTCATCTCCATC | 2074 |
rs760289293 | snp | C/T | 4.94588e-05 | 0.00497262 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530854 | ACCTGAAAAATAAGA[C/T]AAATTGTCTATTTTG | 2074 |
rs760321018 | snp | A/C | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456424 | AGAAGTAGTCTTAAG[A/C]TGAGCAGCCAGACGT | 2074 |
rs760330629 | snp | A/C | 1.65116e-05 | 0.00287324 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483550 | GGTAAAGTCAGTTTT[A/C]AATAAGAAGTGACAC | 2074 |
rs760332508 | snp | C/T | 4.94401e-05 | 0.00497168 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516763 | GTTGTACAGTTAGGT[C/T]GGCTTTTTTCCATTT | 2074 |
rs760374110 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475883 | GTCATAATATCTGGG[-/A]AAATGCAGCTATGTA | 2074 |
rs760387010 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469335 | TCTCCTGATAGATGC[A/C]CTGAGTAAGATACGG | 2074 |
rs760405498 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468021 | ACCCCCTACTCTGTA[C/T]CATACCCAATGCCCC | 2074 |
rs760408945 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49459056 | AGCAGGGCAGAAGCT[C/T]CCTGCAGGTGCCCGC | 2074 |
rs760414129 | snp | G/T | 3.35182e-05 | 0.00409365 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524719 | AGTGCGGATGAGCTC[G/T]TCCCAGGCAGTCTCC | 2074 |
rs760427504 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513797 | ACAATTCAAGATGAG[A/C]TTTGGGTGGGGACAG | 2074 |
rs760438715 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534737 | AAGCAAAACGATAAC[A/C]AAAAATCAGTCTTGC | 2074 |
rs760439226 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538791 | CTTCCGGTCTCAGGT[A/G]AGGCCGCCGGAAGCG | 2074 |
rs760447998 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495869 | GGGTTACTGCATCTC[C/T]GAGGATGATTATTTC | 2074 |
rs760448231 | snp | A/G | 1.78672e-05 | 0.00298886 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517158 | ATTAGTCCTAGTGGT[A/G]GTGGTTTTGCCTAGT | 2074 |
rs760457758 | snp | C/T | 0.00013295 | 0.00815214 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528367 | TCCACTGACTACAGG[C/T]ATCAGGCATCAATTC | 2074 |
rs760476402 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464196 | GGAGATGAGGAACTT[C/G]TTGGGAATTGGAGCA | 2074 |
rs760573030 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521309 | TTTGGTCTTCTGGGC[C/T]ACACAGGGCTGTCTT | 2074 |
rs760574167 | snp | C/T | 1.71402e-05 | 0.00292742 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482665 | TTAAAATGCCAAAAG[C/T]ATTATCATCCTAATA | 2074 |
rs760618206 | snp | A/C | 3.29495e-05 | 0.00405877 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524514 | TATTTTGCACTGGGG[A/C]TGGAGGCGTGACTGG | 2074 |
rs760635712 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476433 | TTAATGATATCCCTA[A/T]TATTAATATTAAAAC | 2074 |
rs760636508 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459348 | GCCAGGGTGGTGAGG[C/T]TGACAGGGTGAGACT | 2074 |
rs760651771 | snp | G/T | 1.69925e-05 | 0.00291478 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532985 | ACAGACTACCTAAAA[G/T]GAAAAAAATTTATAA | 2074 |
rs760663515 | snp | C/T | | | splice-acceptor-variant | ERCC6 | GRCh38.p7 | 10:49532980 | TCTCTACAGACTACC[C/T]AAAAGGAAAAAAATT | 2074 |
rs760686954 | snp | G/T | 1.65037e-05 | 0.00287256 | missense | ERCC6 | GRCh38.p7 | 10:49471086 | GTTTTGGGTCTTTTA[G/T]CACTCTATTTGTCAA | 2074 |
rs760694729 | snp | C/T | 4.94352e-05 | 0.00497143 | missense | ERCC6 | GRCh38.p7 | 10:49471049 | AGCTCATAGAGATCA[C/T]TGGATTTGAAAAACC | 2074 |
rs760714732 | snp | C/T | 1.67371e-05 | 0.0028928 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461486 | TCGGTTGGCTTCTGC[C/T]TCCACCAGTACATAA | 2074 |
rs760722500 | snp | A/G | 1.66585e-05 | 0.00288599 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505855 | ATGGCTTGATAGCAA[A/G]TAGAAAGGAAAGAAC | 2074 |
rs760741490 | in-del | -/CT | 1.66333e-05 | 0.00288381 | frameshift-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524296 | CTCCTCTTCCTCCTC[-/CT]CTGTGGGGAAATACT | 2074 |
rs760747074 | snp | A/G | 1.66103e-05 | 0.00288182 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516368 | ATTAAGTTTGCTTAT[A/G]AGAGGTCGCAATTTG | 2074 |
rs760764489 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527471 | CCTGACGTCAGGAGT[C/T]CGAGACCAGCTTGGC | 2074 |
rs760776669 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49483299 | GTTTATTCTGAATTA[A/G]TTATTCTTCTCCACT | 2074 |
rs760790493 | snp | A/G | 3.30098e-05 | 0.00406249 | missense | ERCC6 | GRCh38.p7 | 10:49461397 | CTGTGGCCAGTCCAG[A/G]TGGGAACACCAGACA | 2074 |
rs760794847 | in-del | -/TT | 1.64886e-05 | 0.00287124 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49515787 | TGAACTTGTATCTTC[-/TT]TTTCAGTTTCTGGGA | 2074 |
rs760800566 | snp | C/T | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517039 | CAGGTGGTTGTATCA[C/T]TATAGCACTTGCTTC | 2074 |
rs760818930 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528188 | GTAATAATAAATGTG[G/T]ACCAGCAGCCTCCTA | 2074 |
rs760845109 | snp | C/T | 3.30104e-05 | 0.00406252 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524362 | TGGCCTCATGTCTGA[C/T]TCCCAAGGTCTCCTT | 2074 |
rs760862544 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496786 | GCACTCCAGCCTGGG[C/T]GACAAGAGCGAGACT | 2074 |
rs760864532 | snp | A/G | 1.64944e-05 | 0.00287175 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49493180 | CGGAGGCCACCACGT[A/G]TGAAATTCCTTCACC | 2074 |
rs760871378 | snp | A/G | 4.94205e-05 | 0.0049707 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532740 | GATCTGATGTCGGTC[A/G]ATGTGCAGCAGGGCT | 2074 |
rs760916788 | snp | A/G | 1.67047e-05 | 0.00288999 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493290 | AAAACAACCATGAAA[A/G]AGCATATACAGTCAT | 2074 |
rs760919459 | in-del | -/CCA | 4.94841e-05 | 0.00497389 | cds-indel | ERCC6 | GRCh38.p7 | 10:49493171 | CACTCTGAACGGAGG[-/CCA]CCACGTGTGAAATTC | 2074 |
rs760952496 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534539 | AAAAGTATCTATCCT[C/G]CACACAGAATGATCT | 2074 |
rs760984582 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515488 | AACGTGAGTCAATGT[C/T]ACGCTTCTGAGGTCT | 2074 |
rs760987098 | snp | A/G | 3.29489e-05 | 0.00405874 | missense | ERCC6 | GRCh38.p7 | 10:49483393 | GATTTCGAATTTTGT[A/G]TCCTTCGTCCAAGAT | 2074 |
rs761011283 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523261 | TGCGCGGCAGTAGCA[C/T]AGTGTTCAGTGGGCC | 2074 |
rs761014144 | snp | C/T | 3.29881e-05 | 0.00406115 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515808 | AGTTTCTGGGAGTAA[C/T]GACTGACAAGACACA | 2074 |
rs761020864 | snp | C/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521485 | AAGAAAGCACTAGAC[C/G]TCACAACCAACAGCC | 2074 |
rs761031098 | snp | A/C | 1.64735e-05 | 0.00286993 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532650 | AAGCACTCCCTGTTC[A/C]AGCACGTCCTGGTCA | 2074 |
rs761086051 | snp | A/T | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49470363 | TTGCTTTGGTCTCAG[A/T]TGTTTCTCCAGGGTC | 2074 |
rs761115470 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460863 | CACTGCACTCCAGCC[C/T]GGGCGAAAGGGCGAG | 2074 |
rs761147930 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504920 | GAGAAAAATTAAAAC[G/T]ATAATATAAGCTCTT | 2074 |
rs761149571 | snp | C/G | 1.65367e-05 | 0.00287543 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516493 | CCAGTACATTATGCA[C/G]ATCTGTTCTTTGTTC | 2074 |
rs761173103 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49472680 | TTGTAACTTTGCCTA[C/T]GTTCTTTTTACCCCA | 2074 |
rs761205667 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503621 | TGAGGAATATAAGGG[C/T]CTGAGCTCAGGTTTC | 2074 |
rs761237267 | snp | A/G | 3.62194e-05 | 0.0042554 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533009 | TTTATAAGCCTTTTC[A/G]TTATATAGGATTCAT | 2074 |
rs761262528 | snp | A/G | 1.66341e-05 | 0.00288388 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472927 | CGTGTCCGTGCTTGG[A/G]TTCCAGTCTGGGTCA | 2074 |
rs761264402 | snp | G/T | 3.29484e-05 | 0.00405871 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49478435 | TGGATTTATGGTATC[G/T]CGTAAGACACATGCA | 2074 |
rs761266024 | snp | C/T | 1.64876e-05 | 0.00287116 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470133 | CTAGAAACAGCCTAC[C/T]CATTTTCTAATCCTA | 2074 |
rs761280736 | snp | C/T | 1.65482e-05 | 0.00287643 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472505 | ACCTCTCAACGAGAA[C/T]CCTTCCCAATGACAA | 2074 |
rs761303700 | snp | C/T | 1.72624e-05 | 0.00293784 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524773 | AAGACTGGATGGCCC[C/T]GGCTCTGAAAGAACA | 2074 |
rs761312431 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459728 | ACTTGCCTTAAAAAA[A/C]CACAAATCTAACTCT | 2074 |
rs761317350 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503572 | GCACTAGCCACACAG[C/T]TGGTAGATGATATAC | 2074 |
rs761332161 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512658 | ACAAGAAGTGTTTTG[A/G]ATTTTGGAATATTTG | 2074 |
rs761366414 | snp | C/G | 1.65263e-05 | 0.00287452 | missense | ERCC6 | GRCh38.p7 | 10:49505944 | TCAAATTCAGCATCA[C/G]TTTCCTCAGAATCGT | 2074 |
rs761491564 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511482 | TCAGCTGGAGTACAG[C/T]GGCACGATCTCAGCT | 2074 |
rs761501309 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512832 | CTGAGACCCAACATA[C/T]GAGGTCAAATATGGA | 2074 |
rs761530292 | snp | A/G | 4.99338e-05 | 0.00499644 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505861 | TGATAGCAAATAGAA[A/G]GGAAAGAACATATGG | 2074 |
rs761533924 | snp | A/G | 1.66275e-05 | 0.00288331 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516190 | GATACGGCTGAAACC[A/G]GCAAATGTAGCCCAG | 2074 |
rs761551271 | in-del | -/AGC | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49483276 | AAATGTGTTACTAAA[-/AGC]AGATAGTTTATTCTG | 2074 |
rs761551318 | in-del | -/TCT | 3.29579e-05 | 0.00405929 | cds-indel | ERCC6 | GRCh38.p7 | 10:49459170 | GATGAAGAGTCTGCA[-/TCT]TCTGCTCTTCCACTA | 2074 |
rs761558075 | snp | A/C | 0.000131791 | 0.00811655 | missense | ERCC6 | GRCh38.p7 | 10:49473585 | TTCAAGTATGTCCAG[A/C]ATCTGTTTGGAGGTG | 2074 |
rs761559473 | snp | G/T | | | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516065 | GAAAAAGTTATTGAA[G/T]ACAAAATGGTATTGT | 2074 |
rs761638923 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | ERCC6 | GRCh38.p7 | 10:49470703 | AAAGGATCACTTCGA[C/T]TAGAAGTTACTGCAT | 2074 |
rs761648306 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482858 | GATCCGATGAGGGGT[A/G]CGAAACTATTTGAGG | 2074 |
rs761666051 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507045 | GAGTAAGAGAGAATG[A/T]CCGAGGGAAGGCAAG | 2074 |
rs761682827 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498341 | ATACATAGCCAATGA[A/G]GCAATAACAGCTCAC | 2074 |
rs761687557 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524929 | ATGTTACATATGAAG[A/G]ACAGAATAAAATTAT | 2074 |
rs761747683 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495816 | CTCTCCGTCTACACT[C/G]TTGCTATGCCAGGTC | 2074 |
rs761802751 | snp | C/T | 0.000148257 | 0.00860851 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49473489 | TACCTCATTGTATCT[C/T]GTAATCAGTGGCTGT | 2074 |
rs761812362 | snp | A/G | | | missense | ERCC6 | GRCh38.p7 | 10:49474085 | TGCCATATTTTCAAC[A/G]AAGACTCAACAACAA | 2074 |
rs761818774 | in-del | -/A | 1.65108e-05 | 0.00287317 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483297 | AGTTTATTCTGAATT[-/A]AATTATTCTTCTCCA | 2074 |
rs761826726 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496709 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATCAC | 2074 |
rs761827662 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | ERCC6 | GRCh38.p7 | 10:49470239 | TCTGTTCCTTGGCCT[C/T]ACTCTTGTTTTCACT | 2074 |
rs761835666 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467592 | ATTTTTTGACATGGG[G/T]TCTCGCTCTGCTGCC | 2074 |
rs761872221 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500837 | GATGTGTGTTTTACA[C/T]GAGTATTATATTTAT | 2074 |
rs761875153 | in-del | -/CT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503132 | ACATGGGTCCAACAA[-/CT]CTTTTTGCTTGGGGC | 2074 |
rs761916831 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495715 | CCTAGGCCTCATCCT[C/T]GAGCAGACCTGCTTG | 2074 |
rs761938604 | in-del | -/ATATATGTTACCTAGAAAA | | | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515163 | TTTTGCATGAAATTC[-/ATATATGTTACCTAGAAAA]ATTCAAGGAACAAAA | 2074 |
rs761939734 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527219 | CCCTAAGAGGTAGCT[A/G]TTAACCCTACTACCA | 2074 |
rs761941049 | snp | A/G | 1.6554e-05 | 0.00287693 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472948 | GTCTGGGTCATAGAT[A/G]ACAACTCTGTTTGCC | 2074 |
rs761954307 | in-del | -/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540349 | CGGCTTGTAACTTGC[-/T]TTTTTTTTTTTTTAA | 2074 |
rs761993386 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508416 | CCCTCCCTCCTAAAA[C/T]ATACAGGCATCTTGT | 2074 |
rs761999259 | in-del | -/CA | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517365 | ATGTTTCTGAAAACT[-/CA]CATCACTTTTTGACA | 2074 |
rs762018091 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490073 | TGAACTTTTATTAAA[C/T]GCGATTTCAAGTGAC | 2074 |
rs762027586 | snp | C/T | 1.65734e-05 | 0.00287862 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461453 | GAGCCTCAGTGCTTT[C/T]AGGGCATCCTGGGCC | 2074 |
rs762052677 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459680 | TCTTCACTTTTAAGT[C/T]TTCTTACTCTTTCCT | 2074 |
rs762128995 | snp | C/T | 3.30044e-05 | 0.00406216 | missense | ERCC6 | GRCh38.p7 | 10:49476259 | CTTCTTTGGAATCAA[C/T]GAAATTTTGGTAGAC | 2074 |
rs762130912 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463370 | TTTTGGATTTTAGAG[C/G]ATTTTAGATTTCAGG | 2074 |
rs762142534 | in-del | -/ACTG | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469105 | ACCATTGTAGTAATA[-/ACTG]ACTGAGGAAAGAATC | 2074 |
rs762156132 | snp | C/G | 1.64923e-05 | 0.00287156 | missense | ERCC6 | GRCh38.p7 | 10:49500593 | GACCTGCCAAGAAGG[C/G]AATTATCTGGATGGT | 2074 |
rs762167817 | snp | A/G | 6.58913e-05 | 0.00573945 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524522 | ACTGGGGCTGGAGGC[A/G]TGACTGGGGCTGGAG | 2074 |
rs762176711 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524076 | CTCCATCATCTCGGT[A/G]TCTTCCCACTTTCCG | 2074 |
rs762204590 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503414 | AAAAAAAATCTTACT[A/G]GGCAGCATGTAAGTC | 2074 |
rs762205885 | snp | C/T | | | missense | ERCC6 | GRCh38.p7 | 10:49470887 | GAACATCTGATCCAG[C/T]TCCTGTAAAGAGGAA | 2074 |
rs762222276 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459064 | AGAAGCTTCCTGCAG[A/G]TGCCCGCTTTCACTT | 2074 |
rs762238572 | snp | C/T | 1.65209e-05 | 0.00287405 | missense | ERCC6 | GRCh38.p7 | 10:49473019 | GAAGAAACACAAATA[C/T]GGATGTGTCCTAGAG | 2074 |
rs762249711 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486339 | CTATACAAAGAATAT[C/T]CATTCTTTACAAACA | 2074 |
rs762265637 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528082 | ATGCGATTAATGATG[C/T]TGGGCTTCCAACATG | 2074 |
rs762272573 | snp | G/T | 1.64893e-05 | 0.0028713 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530859 | AAAAATAAGATAAAT[G/T]GTCTATTTTGCACTC | 2074 |
rs762273270 | snp | C/T | 2.36532e-05 | 0.0034389 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488138 | ATTAATAGGGTACAT[C/T]TGCAATTAGCCTGAC | 2074 |
rs762277865 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | ERCC6 | GRCh38.p7 | 10:49530770 | TCCTGTTGATGTCTC[C/T]GCTGGTGGCAGCTTG | 2074 |
rs762283738 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515493 | GAGTCAATGTTACGC[C/T]TCTGAGGTCTTCCTT | 2074 |
rs762286899 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | ERCC6 | GRCh38.p7 | 10:49459143 | AAGAGTGAGGAGGAA[A/G]CGAGGGGCCCGGATG | 2074 |
rs762322440 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478888 | TCTCCAAAAGCTACA[A/G]AGGAACTCTGCAAAG | 2074 |
rs762332442 | in-del | -/TTTCTCATCATATGT | 1.64776e-05 | 0.00287028 | intron-variant, cds-indel | ERCC6, PGBD3 | GRCh38.p7 | 10:49515590 | CAGAAAATCCACTGG[-/TTTCTCATCATATGT]TTTCTCATCATATGT | 2074 |
rs762337440 | snp | C/G | | | missense | ERCC6 | GRCh38.p7 | 10:49459007 | GATGAAGTTTCTCAT[C/G]TCCACCAGAAGGTCA | 2074 |
rs762351237 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | ERCC6 | GRCh38.p7 | 10:49539460 | GGCTGTGACCTCTCT[A/T]GTTGTCTCCCACGAC | 2074 |
rs762375322 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49482984 | TCTTGCATCATTTTG[A/G]TACTCTCCAAAACAT | 2074 |
rs762391469 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516893 | TGAGGGATCATCTGA[A/G]TCAGACTCAGCATCA | 2074 |
rs762401051 | snp | G/T | 1.64776e-05 | 0.00287028 | missense | ERCC6 | GRCh38.p7 | 10:49470548 | CAGATGGCATAGAAG[G/T]TTTGCCTGTTCCTGA | 2074 |
rs762403656 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465268 | CTTGTGTGGGGCCTA[C/T]AGCCCCTTTGTTTTG | 2074 |
rs762424211 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464607 | CCAGAGGCCCAGGGG[A/G]AAAAAGTGGTTTCAC | 2074 |
rs762427240 | snp | C/T | 7.3779e-05 | 0.00607322 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461596 | TGATATTTCACTCTG[C/T]ATGCAAGAAAGACAC | 2074 |
rs762448040 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515759 | GTTATACACTTTGAT[C/T]ATGTTTGGCTGCTGA | 2074 |
rs762461275 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522841 | AACGAAAGCTGTGCT[A/G]AGGGATGACAAATAT | 2074 |
rs762468697 | snp | A/G | 3.33584e-05 | 0.00408388 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528529 | TAGCTGTTGTTCCTT[A/G]AATGGTAAATATAGA | 2074 |
rs762492121 | snp | A/G | 1.66007e-05 | 0.00288098 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506058 | TATTTTGATCACAAG[A/G]CAGATTTAAAAAGAT | 2074 |
rs762497840 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470327 | CTTGGCGTCTCTGCA[A/G]TGCTTAGAGTTCTTA | 2074 |
rs762581693 | snp | A/G | 1.66117e-05 | 0.00288194 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516344 | TGGAACAAATTTCAT[A/G]CATCTCTCATTAAGT | 2074 |
rs762588948 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470261 | GTTTTCACTGTCTTG[C/T]TTCTGGTAACGCCTT | 2074 |
rs762605407 | snp | A/G | 1.64944e-05 | 0.00287175 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472381 | GTGCACTGACCGGTG[A/G]TAGATCTTTTCTTCA | 2074 |
rs762636359 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477845 | CATCAAAGGTCTTCT[C/G]TGACCAACCCTTACA | 2074 |
rs762670764 | snp | C/T | 4.94556e-05 | 0.00497246 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515939 | GCCTCTTTCTTTTTT[C/T]TTTAAAGCTACATCT | 2074 |
rs762707884 | snp | A/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521587 | CCACTGACCATAGAA[A/C]CGACAGAACATTTAC | 2074 |
rs762728438 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491469 | AAAACACTGAAAAAA[A/T]TATTAACAACCATAT | 2074 |
rs762732111 | snp | A/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518255 | TTGGGTTGGAGTTGG[A/C]CCCCATCAAGTGGAG | 2074 |
rs762734699 | snp | A/G | 3.30355e-05 | 0.00406407 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49505958 | ACTTTCCTCAGAATC[A/G]TCCTCCAGCTTCAGA | 2074 |
rs762778648 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486818 | ATCCTATTACTGAAA[C/T]TGTTCCAAAATATAG | 2074 |
rs762847890 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498710 | TCATTATTAGCCTTG[A/G]CTTCATTCTTAGTAG | 2074 |
rs762873142 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485305 | AGTCAGAATTCGAAC[A/G]GAGAAAGGCAGCCAA | 2074 |
rs762883464 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49466992 | CACCATGTTGTCCAG[A/G]TTGGTCTCGAACTCC | 2074 |
rs762888361 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521298 | CACATGAAATGTTTG[A/G]TCTTCTGGGCCACAC | 2074 |
rs762976316 | snp | A/G | 4.94197e-05 | 0.00497066 | stop-gained | ERCC6 | GRCh38.p7 | 10:49458898 | TTCTCAATAGTTCTC[A/G]GAAGACACAAGACTG | 2074 |
rs762980922 | snp | C/T | 1.64969e-05 | 0.00287196 | missense | ERCC6 | GRCh38.p7 | 10:49474031 | TGTGCACTCACCTGC[C/T]TTGACTGAGAAAACA | 2074 |
rs762983338 | snp | C/T | 6.59065e-05 | 0.00574012 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473447 | CGTACAGCAGCACCA[C/T]TCAACTTCCCTGTTA | 2074 |
rs762994748 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512358 | CCATACTGCAATCCT[G/T]ACCTACCTACACTTA | 2074 |
rs763001005 | snp | A/T | 1.64806e-05 | 0.00287054 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473612 | GGTGGGGGATAGGAG[A/T]TTGCAAAGCAAATAC | 2074 |
rs763008525 | snp | C/T | 1.6549e-05 | 0.0028765 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530884 | GCACTCTGATAACAT[C/T]TTTATAGCATAATAT | 2074 |
rs763025009 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494198 | CATTGTATGATCTCG[A/G]GCACACCATTTAACC | 2074 |
rs763026364 | in-del | -/AAAGAT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49530947 | ACTTCTTATTAACTA[-/AAAGAT]AAAGGAAACTAAACC | 2074 |
rs763043194 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506760 | ACCCATTTAACCAGA[C/G]TAATTTTGCATTTAC | 2074 |
rs763049883 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463192 | CAAAATGTATATATT[G/T]TTAACATACACCTTA | 2074 |
rs763053884 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458606 | AAAAATCAATCCAAG[C/T]ATTTTCTCCTTTAGC | 2074 |
rs763065346 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461952 | TCCCTTGCATTTGAG[C/T]AGAATGACTCAATAA | 2074 |
rs763080690 | in-del | -/ACACACACAT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527854 | ACAATTTGTACACAC[-/ACACACACAT]ACACACACACAATGA | 2074 |
rs763101990 | in-del | -/A | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517873 | GAAAAATGAACTCTC[-/A]AGAGATGTTAAGAAC | 2074 |
rs763115987 | in-del | -/TAA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501096 | ATAAAAAAGGGGCAC[-/TAA]TGTTTATTTTTTCAA | 2074 |
rs763131156 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470588 | ACATTCCCCATTTCC[A/G]CTAATCACTGACAAC | 2074 |
rs763148402 | snp | C/G | 1.64787e-05 | 0.00287038 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515506 | GCTTCTGAGGTCTTC[C/G]TTTTTGGCCAGGTTC | 2074 |
rs763159056 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501669 | CTTGAATTAAAAGAT[A/G]ATAGGTTAGATGAGG | 2074 |
rs763173935 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499371 | AAATAAAACACTAAA[C/T]TCTGGAGACTAAAGA | 2074 |
rs763176329 | snp | A/T | 1.65198e-05 | 0.00287395 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478521 | ATGTTTAAGGAACGC[A/T]TTTGTTCTTACCTCT | 2074 |
rs763244874 | snp | A/G | 1.66729e-05 | 0.00288724 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524300 | TCTTCCTCCTCCTCT[A/G]TGGGGAAATACTCAG | 2074 |
rs763245675 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474845 | CAAGGGGTGAGTGCC[C/G]CGGCCCATCCCCACA | 2074 |
rs763263119 | snp | C/T | 1.67885e-05 | 0.00289724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471155 | GCTGGTATAAAACAA[C/T]GTGTAGCTCTACCTA | 2074 |
rs763264917 | in-del | -/A | 1.74656e-05 | 0.00295508 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482660 | AAATATTAAAATGCC[-/A]AAAGTATTATCATCC | 2074 |
rs763307339 | snp | A/G | 1.6478e-05 | 0.00287032 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516651 | TTGACAATGAGTTCA[A/G]TGACCTCGTCATCAA | 2074 |
rs763337935 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473972 | ATCCCATTTTGTGAG[A/T]TGATGGCTGTCATAA | 2074 |
rs763387298 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481897 | CCCTCACCCCAGTGG[-/T]TCCTGCAGGTCACTC | 2074 |
rs763394450 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | ERCC6 | GRCh38.p7 | 10:49470673 | ACATTACTACTCATG[C/T]GAGGGTCATCTTTCA | 2074 |
rs763434593 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526937 | AATAGATAACCAGGG[A/T]GAGGCAGTAGAACAA | 2074 |
rs763479105 | in-del | -/TG | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473966 | GATTGAATCCCATTT[-/TG]TGAGTTGATGGCTGT | 2074 |
rs763486269 | snp | C/G | 1.64958e-05 | 0.00287187 | missense | ERCC6 | GRCh38.p7 | 10:49493174 | TCTGAACGGAGGCCA[C/G]CACGTGTGAAATTCC | 2074 |
rs763507073 | snp | A/T | 3.33228e-05 | 0.0040817 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505856 | TGGCTTGATAGCAAA[A/T]AGAAAGGAAAGAACA | 2074 |
rs763535359 | in-del | -/A | 0.0177088 | 0.0924165 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472888 | CTAATACATTCTTTT[-/A]AAAAAAAAATAAAAA | 2074 |
rs763537022 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485746 | CTAAAAACTAGAAAA[C/T]AGAATGTAGAACTAT | 2074 |
rs763595372 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525639 | AATTCTTGCAGGCCA[A/G]TGATACCCAGTTTTT | 2074 |
rs763603166 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467430 | AGAGGGTGTATAGTG[C/G]TATCTCGTTATGGTT | 2074 |
rs763614300 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477976 | TATACCTTTTTGTGA[C/T]ACTCTCCCTCAAGAA | 2074 |
rs763629907 | snp | G/T | 1.64741e-05 | 0.00286998 | missense | ERCC6 | GRCh38.p7 | 10:49532863 | CCCATCACCACCACT[G/T]TCTTGCTTGATTGCC | 2074 |
rs763631188 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498723 | TGACTTCATTCTTAG[C/T]AGGATTGTCACCACC | 2074 |
rs763644445 | snp | C/T | 1.67508e-05 | 0.00289398 | missense | ERCC6 | GRCh38.p7 | 10:49461488 | GGTTGGCTTCTGCCT[C/T]CACCAGTACATAATC | 2074 |
rs763672096 | snp | A/G | 4.94947e-05 | 0.00497443 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49500636 | CATTTCATCTCCCAG[A/G]ATTCCTCCTGCCTGC | 2074 |
rs763706028 | snp | A/G | 1.66477e-05 | 0.00288506 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516118 | CCTCACTAAACTGAA[A/G]GACAAGTGACGCACC | 2074 |
rs763754676 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534455 | TGTAACTACTAAGTA[C/T]ATTCTGTATACTGAT | 2074 |
rs763758370 | snp | A/C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521610 | ACATTTACTTCTAAG[A/C/T]AGTGGCTCATCCATC | 2074 |
rs763796002 | snp | A/C | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524068 | ATCTTCATCTCCATC[A/C]TCTCGGTATCTTCCC | 2074 |
rs763810265 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470621 | TTCTGGTCCAGATAC[C/T]GCATTTGTCTCTTCT | 2074 |
rs763811839 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | ERCC6 | GRCh38.p7 | 10:49473481 | TCACATGTTACCTCA[C/T]TGTATCTCGTAATCA | 2074 |
rs763844578 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49505220 | ATTTACATTCATCAC[A/G]GGAGACTGGCCAGCC | 2074 |
rs763844787 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474189 | CTTGGGACCTCCAGA[A/G]AAGAGATCAGGGTGG | 2074 |
rs763872687 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529918 | AAAATAATATCCTAA[C/G]TAACAAATATTCCCT | 2074 |
rs763892806 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499427 | TTCATATTTGGCTCT[C/T]TACTAAGCATTTCGC | 2074 |
rs763904611 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512696 | ACAATGAGATATGTT[A/G]GGATGGGACCCAAGA | 2074 |
rs763905070 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49493516 | GAGATATAACATCTA[C/T]AGTAACATAAAAGAT | 2074 |
rs763920726 | snp | A/G | 0.000148274 | 0.008609 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515642 | TTGTAAGACCAGTTC[A/G]AAACAGAACAAAAGA | 2074 |
rs763990339 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486988 | CCTACTAAAGGCTTA[C/T]CACAGGAATACAAGA | 2074 |
rs764009660 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528116 | TTTAATCATGATGCT[A/T]GTTGTCTTTATCAAA | 2074 |
rs764038080 | in-del | -/T | 1.82158e-05 | 0.00301787 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472898 | CTTTTAAAAAAAAAA[-/T]AAAAACAAACCTGCG | 2074 |
rs764038554 | snp | C/T | 3.29478e-05 | 0.00405867 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524640 | ATGCTTCATTAAGCA[C/T]GATTTTTCTGGGCTT | 2074 |
rs764038676 | snp | A/C | 1.75866e-05 | 0.0029653 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533002 | AAAAAAATTTATAAG[A/C]CTTTTCGTTATATAG | 2074 |
rs764040546 | snp | G/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455080 | ACTATATTTTAAAAC[G/T]TCCGTATGATAAACA | 2074 |
rs764062385 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480684 | ATCTGGCCAACACCA[C/T]CTTAAAGTAATCAGA | 2074 |
rs764074538 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485312 | ATTCGAACGGAGAAA[A/G]GCAGCCAAATCCAAA | 2074 |
rs764106200 | in-del | -/T | | | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515147 | TTACAATTTTTTGAA[-/T]TTTTGCATGAAATTC | 2074 |
rs764124941 | snp | C/T | 3.62168e-05 | 0.00425524 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515302 | TAATGTATAAAACTA[C/T]GTTTCTTATCTCAGG | 2074 |
rs764134449 | snp | C/G | 1.66076e-05 | 0.00288158 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516370 | TAAGTTTGCTTATGA[C/G]AGGTCGCAATTTGGA | 2074 |
rs764159237 | snp | A/G | 4.94915e-05 | 0.00497426 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524368 | CATGTCTGACTCCCA[A/G]GGTCTCCTTGCCTTT | 2074 |
rs764196826 | snp | A/G | 7.52899e-05 | 0.00613508 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461597 | GATATTTCACTCTGT[A/G]TGCAAGAAAGACACT | 2074 |
rs764199614 | snp | C/G | 3.30726e-05 | 0.00406635 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516498 | ACATTATGCACATCT[C/G]TTCTTTGTTCCCAAA | 2074 |
rs764243644 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506898 | TGATGCTCTGAATTT[C/T]ACAAAATGGTGGAAA | 2074 |
rs764246480 | in-del | -/ATG | 1.64765e-05 | 0.00287019 | cds-indel | ERCC6 | GRCh38.p7 | 10:49470396 | TTCTTCTGCCACACT[-/ATG]ATGTTTTGTTTTTGA | 2074 |
rs764269466 | snp | A/T | 1.67041e-05 | 0.00288994 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493291 | AAACAACCATGAAAG[A/T]GCATATACAGTCATC | 2074 |
rs764295401 | snp | A/G | 3.29468e-05 | 0.00405861 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524517 | TTTGCACTGGGGCTG[A/G]AGGCGTGACTGGGGC | 2074 |
rs764319566 | snp | A/G | 0.000131785 | 0.00811635 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524617 | TGCCAAATACTTTTC[A/G]AAGCCTGATGCTTCA | 2074 |
rs764335032 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502512 | ACAGCCTCACAATCA[A/G]CTTGCACAAAGGAGA | 2074 |
rs764344857 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501148 | GCAGGACAGAGAACA[A/C]CACAACCTATAGCTT | 2074 |
rs764355661 | snp | A/G | 1.71513e-05 | 0.00292837 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460497 | AATGTTTGCTTTTGA[A/G]ACTTAGAGATCAAAA | 2074 |
rs764394351 | snp | C/T | 1.64928e-05 | 0.00287161 | missense | ERCC6 | GRCh38.p7 | 10:49470467 | CCCAAAAAGCTTCTG[C/T]TTGAGCCTGGCTGGG | 2074 |
rs764418341 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462045 | ATGAAGCTAGACAAA[C/G]TGACACTAAAGTTCA | 2074 |
rs764425226 | snp | C/T | 1.65135e-05 | 0.00287341 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483553 | AAAGTCAGTTTTAAA[C/T]AAGAAGTGACACCCT | 2074 |
rs764437003 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | ERCC6 | GRCh38.p7 | 10:49530767 | GTTTCCTGTTGATGT[C/T]TCTGCTGGTGGCAGC | 2074 |
rs764456630 | snp | A/C | 1.65026e-05 | 0.00287246 | missense | ERCC6 | GRCh38.p7 | 10:49476262 | CTTTGGAATCAACGA[A/C]ATTTTGGTAGACTTT | 2074 |
rs764464618 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473359 | AAGTCTCCCCTTAGG[A/C]CCCCTCCCAAGCCCA | 2074 |
rs764483314 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458356 | TGGTAAATATAAATG[C/T]TTAAAGTTTAAGCAT | 2074 |
rs764527910 | snp | C/G | 8.93823e-05 | 0.00668455 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517159 | TTAGTCCTAGTGGTA[C/G]TGGTTTTGCCTAGTG | 2074 |
rs764531698 | snp | C/T | 1.65858e-05 | 0.00287969 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515385 | AAGGCAACATCACAT[C/T]TTTCACATCGAAAAG | 2074 |
rs764536593 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469622 | TTAAACTGAGTACCA[C/T]AAGCAGCAATCTTTG | 2074 |
rs764585949 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501673 | AATTAAAAGATGATA[C/G]GTTAGATGAGGTGGC | 2074 |
rs764600039 | snp | C/T | 1.73444e-05 | 0.00294481 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528561 | GACAGAAAACAGCAA[C/T]GAAGTGATTTATTGT | 2074 |
rs764632858 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49458959 | CAGTATCTCCCTGGT[A/G]CTGGCCTGGCCATCA | 2074 |
rs764636798 | in-del | -/GAAC | 1.64855e-05 | 0.00287097 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49482735 | GGTGATGGGGACGGA[-/GAAC]TGCTCCATAAACACA | 2074 |
rs764647091 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526212 | TTTCCAAAGTGTTAC[A/G]TTCCAAAGTCCCCAT | 2074 |
rs764700976 | snp | C/T | 3.29549e-05 | 0.00405911 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516815 | CCTCCTCCTTGATGG[C/T]GGAGGTTGCTGCACA | 2074 |
rs764730706 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525643 | CTTGCAGGCCAATGA[C/T]ACCCAGTTTTTCATT | 2074 |
rs764735348 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476631 | GCTCAAACCATCCCA[C/T]CTCCCATGACCCATG | 2074 |
rs764808047 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510263 | TGCTGCCATTTAAAG[G/T]TAATTTATTTTAGAA | 2074 |
rs764824370 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482780 | TAACTTTCCCGGGAA[A/G]ATGAAGTCAAAGAGC | 2074 |
rs764824796 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49532200 | TGAAGGGGGCGCAAT[A/G]TATTCCTGGCATCTC | 2074 |
rs764831387 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470146 | ACTCATTTTCTAATC[C/T]TAGCATCCCTGTGGC | 2074 |
rs764842788 | snp | C/T | 1.65228e-05 | 0.00287422 | missense | ERCC6 | GRCh38.p7 | 10:49505945 | CAAATTCAGCATCAC[C/T]TTCCTCAGAATCGTC | 2074 |
rs764889111 | snp | A/G | 1.8764e-05 | 0.00306295 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533016 | GCCTTTTCGTTATAT[A/G]GGATTCATTGTAGTT | 2074 |
rs764894839 | snp | C/T | 1.66142e-05 | 0.00288216 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516198 | TGAAACCAGCAAATG[C/T]AGCCCAGACAGGTGG | 2074 |
rs764896064 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508914 | AGAGACTTTAAGGGC[C/T]CTCTTTAACATGTCT | 2074 |
rs764923278 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471481 | CCTGCCTAGAACCTT[A/C]CTATCATAGGGCTCA | 2074 |
rs764930719 | snp | A/G | 1.66446e-05 | 0.00288479 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505867 | CAAATAGAAAGGAAA[A/G]AACATATGGTACATA | 2074 |
rs764955641 | in-del | -/TCAT | 1.6608e-05 | 0.00288162 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49516351 | AATTTCATGCATCTC[-/TCAT]TAAGTTTGCTTATGA | 2074 |
rs764956689 | snp | C/T | 1.67214e-05 | 0.00289144 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459274 | GATATATTTAATTTC[C/T]AGTTTATGCCCCCAC | 2074 |
rs765012066 | snp | A/G | 6.59234e-05 | 0.00574085 | missense | ERCC6 | GRCh38.p7 | 10:49470803 | CAGGGAACTTCTTGC[A/G]TTTTGGAACATCATG | 2074 |
rs765016273 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473353 | AACAACAAGTCTCCC[C/T]TTAGGCCCCCTCCCA | 2074 |
rs765040780 | in-del | -/ACTGGGGCTGGAGGCGTG | 1.64756e-05 | 0.00287011 | cds-indel, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524507 | TTGTTTTTATTTTGC[-/ACTGGGGCTGGAGGCGTG]ACTGGGGCTGGAGCT | 2074 |
rs765045713 | snp | C/T | | | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49517031 | AGCATTTTCAGGTGG[C/T]TGTATCACTATAGCA | 2074 |
rs765047364 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486401 | AGTCAACTTAGCCTC[-/A]CCAAAAAAGGAAAAT | 2074 |
rs765071536 | snp | G/T | 1.64947e-05 | 0.00287177 | missense | ERCC6 | GRCh38.p7 | 10:49493182 | GAGGCCACCACGTGT[G/T]AAATTCCTTCACCCA | 2074 |
rs765081191 | snp | A/G | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539306 | CCCTGCTGGCAAGGC[A/G]GTTATGAAAGTTAAG | 2074 |
rs765093637 | snp | A/G | 0.000181253 | 0.00951808 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515729 | ATCAGCTCTGTCTAC[A/G]CCTCCCATGAACTGG | 2074 |
rs765116128 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473601 | ATCTGTTTGGAGGTG[A/G]GGGATAGGAGTTTGC | 2074 |
rs765127198 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498625 | TCTGGGATGTAGTCC[A/G]ATATGCCACATTATT | 2074 |
rs765142258 | in-del | -/ACT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504373 | ATATTATTTATATTA[-/ACT]ACTATAGAGTTTTGT | 2074 |
rs765217055 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497226 | GCCCCTTCCATGGCA[C/G]CAAGCCTTTCTAAAA | 2074 |
rs765225415 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490619 | CGGCCTCCCAAAGTG[C/G]TGGGATTACAGGCAT | 2074 |
rs765232010 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461871 | CAATGTGTAAAGCCT[A/G]TATGGAGAAGACATG | 2074 |
rs765234910 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538849 | TGCGTCCTCGCTGAC[A/G]GGCTCAATCACCACG | 2074 |
rs765244441 | snp | G/T | 1.64874e-05 | 0.00287113 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515418 | GTGTTCTTATGACAT[G/T]CAGCGCATCGCGTTT | 2074 |
rs765248544 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473755 | TATTTTTGGTATTTC[C/T]GTATGGTTAATTCTT | 2074 |
rs765252538 | snp | C/G/T | 6.61423e-05 | 0.00575043 | missense | ERCC6 | GRCh38.p7 | 10:49472962 | TGACAACTCTGTTTG[C/G/T]CCCCGTCAGGTTGAC | 2074 |
rs765257036 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525367 | TTTCAAGTGCTCAAG[A/G]GCTACACGTGACTAA | 2074 |
rs765297832 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49505124 | GTAATGGTTTAACTT[C/T]CTATATGCATCTAAG | 2074 |
rs765330902 | snp | A/T | 6.59141e-05 | 0.00574045 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515496 | TCAATGTTACGCTTC[A/T]GAGGTCTTCCTTTTT | 2074 |
rs765420678 | snp | C/G | 1.64811e-05 | 0.00287059 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516640 | AGTTGGAGTACTTGA[C/G]AATGAGTTCAATGAC | 2074 |
rs765438761 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503935 | TGTGGCTGAAAATAA[A/G]GTCAAAAGATTGAAG | 2074 |
rs765477676 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517251 | TATTTTCTTTTTACC[A/G]CACAATAGCATAACT | 2074 |
rs765527879 | in-del | -/TCAAATGATC | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496329 | GAGATAATCTCTTCT[-/TCAAATGATC]TCAATGCCTACCTAA | 2074 |
rs765541703 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477898 | TTGCCCTCAGCATTC[C/T]CAGCTTATCCTTCAA | 2074 |
rs765553096 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499771 | AAGTATTTCAGTCCT[A/G]CCATATCAAATAGAT | 2074 |
rs765577885 | snp | C/T | 8.23906e-05 | 0.00641783 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49471033 | ACTAGTCAGAGTAAA[C/T]AGCTCATAGAGATCA | 2074 |
rs765582564 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525576 | ACATAACCAAAATAC[C/T]AAAAGACCTAAGGCT | 2074 |
rs765589478 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501995 | ATGCAAGATAAGGCA[-/T]TTTTTTTTTCAAAGA | 2074 |
rs765594141 | snp | A/G | 1.65883e-05 | 0.00287991 | missense | ERCC6 | GRCh38.p7 | 10:49474223 | CAAATTTTTCTTAGG[A/G]CTATAAGTCCGGAGA | 2074 |
rs765619125 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499314 | AAAACTCCAAACACT[C/T]CTCACAGAAGTATTG | 2074 |
rs765654184 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509487 | TCAGTTAATTATTAT[A/G]AATAATGTGCTCACC | 2074 |
rs765667650 | snp | C/T | 1.65072e-05 | 0.00287286 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530870 | AAATTGTCTATTTTG[C/T]ACTCTGATAACATTT | 2074 |
rs765687788 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523498 | AGTACACTTTTTGCA[C/T]GATGGTGGCTTATAA | 2074 |
rs765695020 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512820 | ACTGTGTCTTGACTG[A/T]GACCCAACATATGAG | 2074 |
rs765698996 | in-del | -/AG | 0.00682079 | 0.0579989 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472477 | TCCCGGGCCTGCAAC[-/AG]AGAGAGAGAGAGACC | 2074 |
rs765705694 | snp | C/T | 0.000161465 | 0.00898369 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517163 | TCCTAGTGGTAGTGG[C/T]TTTGCCTAGTGTTCC | 2074 |
rs765707223 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467212 | TACAAGCCTTCGTAT[A/G]GACATATTTTTCCAT | 2074 |
rs765729835 | snp | C/T | 2.3486e-05 | 0.00342673 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488141 | AATAGGGTACATCTG[C/T]AATTAGCCTGACTTA | 2074 |
rs765744047 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480575 | ACAAGAACTTCAAGG[-/A]AAAAAAACAGATCAT | 2074 |
rs765783879 | snp | C/T | 3.29582e-05 | 0.00405931 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517024 | GTGCTGTAGCATTTT[C/T]AGGTGGTTGTATCAC | 2074 |
rs765799298 | snp | G/T | 1.64754e-05 | 0.00287009 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49530774 | GTTGATGTCTCTGCT[G/T]GTGGCAGCTTGAGGG | 2074 |
rs765804876 | snp | C/G | 1.64781e-05 | 0.00287033 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459145 | GAGTGAGGAGGAAGC[C/G]AGGGGCCCGGATGAA | 2074 |
rs765825423 | in-del | -/CT | 1.65165e-05 | 0.00287367 | ERCC6 | 10 | allele_origin=T(germline)/(germline) | 10:49461382 | GCACCAGAAATCCCC[-/CT]GTGGCCAGTCCAGGT | 2074 |
rs765843317 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515737 | TGTCTACGCCTCCCA[C/T]GAACTGGTTATACAC | 2074 |
rs765861192 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489999 | ATTAATCAACTCACA[A/T]GAAAGTTGCTCTATA | 2074 |
rs765868122 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535739 | GAAGTTTGGGGAAAA[C/T]TTCTAATAATAAAAA | 2074 |
rs765871505 | snp | C/T | 1.67961e-05 | 0.00289789 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528535 | TTGTTCCTTGAATGG[C/T]AAATATAGAAGACAG | 2074 |
rs765902760 | snp | A/C | 1.64738e-05 | 0.00286995 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459067 | AGCTTCCTGCAGGTG[A/C]CCGCTTTCACTTTCT | 2074 |
rs765940559 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531220 | CCGTTACGGAAGCCT[A/T]CCAAAGTCTGGAAGC | 2074 |
rs765959190 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457838 | CAAACACATAAACAG[C/T]AGTGAGATACAAACA | 2074 |
rs765964365 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487697 | CAAGCTTCCCAAATG[C/T]ATACCACTGGAATGA | 2074 |
rs765965600 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531982 | TTCCCCATTAACGTG[C/T]TATGCTCAAAACAGC | 2074 |
rs765971766 | snp | G/T | 1.64765e-05 | 0.00287019 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516903 | TCTGAGTCAGACTCA[G/T]CATCAGAGCCATCTT | 2074 |
rs765973426 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456462 | AAACTCAAAAATTTT[A/G]TTAGTAAAGGAAGAA | 2074 |
rs765990260 | snp | C/T | 1.65652e-05 | 0.0028779 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528388 | GCATCAATTCAAGAA[C/T]ACAGAGAAACTGCTC | 2074 |
rs765994765 | snp | G/T | 1.64735e-05 | 0.00286993 | missense | ERCC6 | GRCh38.p7 | 10:49473502 | CTCGTAATCAGTGGC[G/T]GTCTTGAAGCTATTG | 2074 |
rs766013810 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536043 | ATCGCTTGAACCCAG[G/T]AGGCAGAGGTTGCAG | 2074 |
rs766106661 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464249 | AGCAAAGAGACAGGC[A/G]GCATTTTGCCCCTGC | 2074 |
rs766118778 | snp | C/T | 1.69029e-05 | 0.00290709 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461312 | TTCTAGCCTTAGTTG[C/T]TTGGACTCCTTGCAA | 2074 |
rs766139602 | snp | C/T | 1.65075e-05 | 0.00287289 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461420 | ACCAGACACTGCTCC[C/T]AGACACCGCTGACGA | 2074 |
rs766162602 | snp | C/G | 1.6492e-05 | 0.00287154 | missense | ERCC6 | GRCh38.p7 | 10:49500600 | CAAGAAGGCAATTAT[C/G]TGGATGGTCTTGCCC | 2074 |
rs766170632 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532656 | TCCCTGTTCCAGCAC[A/G]TCCTGGTCATAGACG | 2074 |
rs766195719 | snp | A/G | 1.64732e-05 | 0.0028699 | stop-gained | ERCC6 | GRCh38.p7 | 10:49478356 | TGGATTTACAGACCT[A/G]TTCATTTTTATCTGG | 2074 |
rs766195906 | snp | C/T | | | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49539053 | CGTGGCGCCTGCGCC[C/T]TCAGCTCAACCATAG | 2074 |
rs766208632 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513547 | GGAAAGAGGTTTAAT[A/T]GACTCACAATTCGGC | 2074 |
rs766226106 | snp | A/G | 1.65299e-05 | 0.00287483 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470898 | CCAGTTCCTGTAAAG[A/G]GGAAAAACACCACTA | 2074 |
rs766256094 | snp | A/G | 0.000148247 | 0.00860822 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524529 | CTGGAGGCGTGACTG[A/G]GGCTGGAGCTTTTCT | 2074 |
rs766263811 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476440 | TATCCCTATTATTAA[C/T]ATTAAAACAACAAAG | 2074 |
rs766264775 | snp | G/T | 1.64735e-05 | 0.00286993 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532763 | GCAGGGCTGGCCCTC[G/T]CCTCGGAGCTGCTGA | 2074 |
rs766274422 | snp | A/C/T | 3.2973e-05 | 0.00406025 | missense | ERCC6 | GRCh38.p7 | 10:49470817 | CGTTTTGGAACATCA[A/C/T]GGTCTGCTCCAAAGG | 2074 |
rs766290139 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537974 | TGATCCACCCACCTC[A/G]GCCTCCCAACAACGT | 2074 |
rs766340265 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509953 | AGCTCCTCACACAAC[C/T]GCCAGATTCAGCCTG | 2074 |
rs766373651 | snp | A/G | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516388 | GTCGCAATTTGGAAA[A/G]TTTGTCCACTGGATC | 2074 |
rs766386554 | snp | C/T | 2.26508e-05 | 0.00336525 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488164 | CTGACTTACTGAATG[C/T]AGTGCTGTTGTCATT | 2074 |
rs766387322 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488429 | TTTAATAAACAAGGA[-/T]TTGTGCTGACAATAA | 2074 |
rs766423401 | snp | A/G | | | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49517046 | TTGTATCACTATAGC[A/G]CTTGCTTCTATGCTG | 2074 |
rs766453599 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480298 | TGCCCTGTACTGGGA[-/C]CCAGGTTTATTTGCC | 2074 |
rs766454521 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520564 | ACCACTGCTGGACAA[A/G]GAGGCAGGAGTCAGT | 2074 |
rs766459533 | snp | G/T | 3.29625e-05 | 0.00405958 | missense | ERCC6 | GRCh38.p7 | 10:49471055 | TAGAGATCATTGGAT[G/T]TGAAAAACCGCCTTT | 2074 |
rs766460731 | snp | C/T | 1.64933e-05 | 0.00287165 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474033 | TGCACTCACCTGCCT[C/T]GACTGAGAAAACAGC | 2074 |
rs766485402 | in-del | -/TG | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455058 | AAAAAATGGAAAGAC[-/TG]AATTTACTATATTTT | 2074 |
rs766516440 | in-del | -/A | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458451 | GTTTTTAGCACCAAT[-/A]AAAAAAAATATTGAG | 2074 |
rs766519322 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528247 | CTCTTTGAGAGGGAT[A/T]TGGTTCTGCAGGTGT | 2074 |
rs766553083 | snp | A/C/T | 6.60288e-05 | 0.00574549 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515992 | TGTGATCCTTTCTCA[A/C/T]TGTACCTGTTGCCTG | 2074 |
rs766558792 | snp | A/G | 3.30502e-05 | 0.00406497 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473033 | ATGGATGTGTCCTAG[A/G]GGTAAGACACACAAC | 2074 |
rs766609334 | snp | G/T | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539209 | CGCCTTTCTACTTGC[G/T]TGCGAGCAGGGCGAG | 2074 |
rs766610549 | in-del | -/T | 1.64909e-05 | 0.00287144 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49515795 | TATCTTCTTTTTCAG[-/T]TTCTGGGAGTAACGA | 2074 |
rs766614166 | in-del | -/AAG | 1.65932e-05 | 0.00288034 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459242 | ATGCCATCCTATAAA[-/AAG]AAGACCACTATACTG | 2074 |
rs766622325 | snp | C/T | 1.65162e-05 | 0.00287365 | missense | ERCC6 | GRCh38.p7 | 10:49505960 | TTTCCTCAGAATCGT[C/T]CTCCAGCTTCAGACG | 2074 |
rs766629930 | in-del | -/GACA | 1.651e-05 | 0.0028731 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49493218 | GCATCACTGTTGTTG[-/GACA]GACAATTACAGTTGG | 2074 |
rs766662529 | snp | C/T | 4.94279e-05 | 0.00497107 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470156 | TAATCCTAGCATCCC[C/T]GTGGCAAACGTATCA | 2074 |
rs766662547 | snp | G/T | 1.64928e-05 | 0.00287161 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472384 | CACTGACCGGTGGTA[G/T]ATCTTTTCTTCAATG | 2074 |
rs766668330 | snp | C/G | 1.64789e-05 | 0.0028704 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515512 | GAGGTCTTCCTTTTT[C/G]GCCAGGTTCTGGAGG | 2074 |
rs766712094 | snp | C/T | 6.62054e-05 | 0.00575312 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516240 | AACTTATAGCCAAAC[C/T]GAATGGGCTTTCCCC | 2074 |
rs766750385 | snp | A/T | 1.67967e-05 | 0.00289794 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471157 | TGGTATAAAACAATG[A/T]GTAGCTCTACCTAAA | 2074 |
rs766772546 | in-del | -/AAGG | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49530190 | TGATGCAGGAAAACT[-/AAGG]AAGTGCGCCCAAGTG | 2074 |
rs766791061 | in-del | -/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519976 | ATTCTGACACACACA[-/C]CCCCACAAGAACCAG | 2074 |
rs766812535 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523350 | ATATGCAATTCAGAC[G/T]TCATGTTTCACATGT | 2074 |
rs766836707 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479228 | CTTAACAACTTAGTA[A/G]ATTACTATTTCATGG | 2074 |
rs766843561 | snp | A/G | 6.66001e-05 | 0.00577023 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516134 | GACAAGTGACGCACC[A/G]ACACCATATTCCTCA | 2074 |
rs766857552 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504946 | CTCTTTGAGAGAAAA[C/T]ATAAAGAGCATGCTG | 2074 |
rs766891583 | snp | C/T | 1.64876e-05 | 0.00287116 | missense | ERCC6 | GRCh38.p7 | 10:49532564 | TCATCCAGGACCGAC[C/T]GATACTCCTTCTCCA | 2074 |
rs766897436 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460985 | ATTCTCAATTCCAAG[C/T]AGGAAAATCATTCTA | 2074 |
rs766909595 | snp | A/C | 1.64827e-05 | 0.00287073 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515968 | CTGATTCCAGTGGAA[A/C]TCTGTCAATGTGATC | 2074 |
rs766959966 | snp | A/G | 0.000407249 | 0.0142639 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475521 | CCAATAAGAAATGAA[A/G]TAAGAAATTGTGAGA | 2074 |
rs766960580 | in-del | -/CTTGCTCC | 1.64751e-05 | 0.00287007 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49532919 | GACTCTGTAAACAGT[-/CTTGCTCC]TGAGTTTGACTTGAG | 2074 |
rs766962879 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474959 | TGAGCAGAGGAGAAA[-/T]CACCATTAAGCCAAT | 2074 |
rs766980240 | snp | C/G | 6.62899e-05 | 0.00575678 | splice-acceptor-variant | ERCC6 | GRCh38.p7 | 10:49459235 | TTTCATGATGCCATC[C/G]TATAAAAAGAAGACC | 2074 |
rs766983463 | snp | C/T | 1.6516e-05 | 0.00287362 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500505 | AATATTAATTGAGCT[C/T]CACAGACTGACAGTC | 2074 |
rs766986601 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538951 | TTCGGCCGGGACCCC[C/T]GAACACTCACCCAGG | 2074 |
rs766997147 | snp | C/T | 7.12949e-05 | 0.00597012 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517154 | TATTATTAGTCCTAG[C/T]GGTAGTGGTTTTGCC | 2074 |
rs767051809 | snp | G/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456263 | TCCATCTCTTGAGAT[G/T]CCAGGTCACTACTGA | 2074 |
rs767069804 | snp | C/T | 1.65334e-05 | 0.00287514 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470908 | TAAAGAGGAAAAACA[C/T]CACTAATACTATATT | 2074 |
rs767074554 | snp | A/C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468007 | ACTACAGAGGCAAGA[A/C/T]CCCCTACTCTGTATC | 2074 |
rs767084788 | snp | A/G | 1.6486e-05 | 0.00287102 | missense | ERCC6 | GRCh38.p7 | 10:49474049 | GACTGAGAAAACAGC[A/G]ATACTCGCTGACCCT | 2074 |
rs767095701 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512694 | ACACAATGAGATATG[C/T]TGGGATGGGACCCAA | 2074 |
rs767113824 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467133 | TTTAACTATTTACTT[A/G]TTGGTAGACATTTGA | 2074 |
rs767117156 | snp | A/C/T | 6.59482e-05 | 0.00574198 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515846 | GATACCAGCACCAGA[A/C/T]GAGGCAACAGTGACA | 2074 |
rs767133566 | snp | C/T | 1.64846e-05 | 0.0028709 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517036 | TTTCAGGTGGTTGTA[C/T]CACTATAGCACTTGC | 2074 |
rs767247987 | snp | A/G/T | 6.58973e-05 | 0.00573978 | ERCC6 | 10 | allele_origin=G(germline)/A(germline) | 10:49483384 | CAGCATTTGGATTTC[A/G/T]AATTTTGTGTCCTTC | 2074 |
rs767256022 | in-del | -/T | | | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517033 | ATTTTCAGGTGGTTG[-/T]TATCACTATAGCACT | 2074 |
rs767287698 | snp | A/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519378 | AAAGACTGGAATGAC[A/C]TGTAGAAAATAAAAA | 2074 |
rs767287936 | snp | A/G | 1.80523e-05 | 0.0030043 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482637 | ATAGTATTTAATAGG[A/G]GCACTTTAAATATTA | 2074 |
rs767298915 | snp | A/G | 3.40182e-05 | 0.00412407 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528546 | ATGGTAAATATAGAA[A/G]ACAGAAAACAGCAAT | 2074 |
rs767306391 | snp | G/T | 3.29717e-05 | 0.00406015 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478487 | TTTAATAAGAGCAGA[G/T]AAGGGAACATTACTA | 2074 |
rs767314325 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488876 | GCAAGTTCCGCCTCC[C/T]AGGTTCACGCCATTC | 2074 |
rs767315813 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508438 | GCATCTTGTCGCCAC[A/C]GAACTCAGCACCTAG | 2074 |
rs767341442 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486563 | AGATGTACAGCATCA[C/G]AAATGTCAAAGGAAC | 2074 |
rs767342762 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536303 | TGGATTTGTTGGGGG[G/T]AGGGAGAGAACTAGG | 2074 |
rs767394327 | snp | A/T | 1.64958e-05 | 0.00287187 | missense | ERCC6 | GRCh38.p7 | 10:49500622 | GTCTTGCCCAATCCC[A/T]TTTCATCTCCCAGAA | 2074 |
rs767400753 | snp | A/C/T | 3.29561e-05 | 0.00405921 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516652 | TGACAATGAGTTCAA[A/C/T]GACCTCGTCATCAAG | 2074 |
rs767409344 | in-del | -/TA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537489 | GACATTTAAAAACTA[-/TA]TATATATATATATAC | 2074 |
rs767415307 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463384 | GCATTTTAGATTTCA[C/G]GTTTTGGGTCAACAT | 2074 |
rs767433676 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462190 | AGACACAACAGGAGA[C/T]TGACCAGAAAATAGA | 2074 |
rs767434918 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490025 | CTATATTAGAAAAAA[-/G]GATCACGAAATATAA | 2074 |
rs767476350 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520349 | TCGTTGCCCTCACTG[C/T]AGTCTGCGAGGGCAG | 2074 |
rs767481856 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49470019 | AAAGAGGTGTAAATA[C/T]GATTTTTAAAATGTC | 2074 |
rs767510414 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473971 | AATCCCATTTTGTGA[C/G]TTGATGGCTGTCATA | 2074 |
rs767542750 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527278 | GCAGATCTGAGACGG[C/T]CAGACAGGAACAAAC | 2074 |
rs767580819 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531210 | TTTTTTAAGCCCGTT[A/G]CGGAAGCCTTCCAAA | 2074 |
rs767583868 | snp | C/G | 1.6477e-05 | 0.00287024 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515719 | CAATGTTTTCATCAG[C/G]TCTGTCTACGCCTCC | 2074 |
rs767587702 | snp | C/T | 3.3162e-05 | 0.00407184 | missense | ERCC6 | GRCh38.p7 | 10:49460434 | AAGTTAGAATTCCTT[C/T]TCTTACCAAATCTAC | 2074 |
rs767598675 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503306 | ATACAATGTGCTGGG[C/T]GTTTCCTCATCTACA | 2074 |
rs767600590 | in-del | -/A | 1.71858e-05 | 0.00293132 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493086 | GGAGGGCATTAAAAC[-/A]AAACAAAAAGGTACT | 2074 |
rs767609722 | snp | C/T | 1.65575e-05 | 0.00287724 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524344 | AGAGTCTCCCTCTGC[C/T]TCTGGCCTCATGTCT | 2074 |
rs767621835 | snp | A/C/T | 0.00033021 | 0.0128452 | missense | ERCC6 | GRCh38.p7 | 10:49461427 | ACTGCTCCCAGACAC[A/C/T]GCTGACGAGAGAGCC | 2074 |
rs767626571 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538739 | CGCTGGCCGGCCAGG[G/T]ACTCAAGCCGCCTCA | 2074 |
rs767647833 | snp | A/G | 1.65154e-05 | 0.00287358 | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524247 | TACCATCTCCAGACA[A/G]GTCCGCCTCTGCCCC | 2074 |
rs767691315 | snp | G/T | 1.65042e-05 | 0.0028726 | missense | ERCC6 | GRCh38.p7 | 10:49476245 | GAGAATCCTGTAAAC[G/T]TCTTTGGAATCAACG | 2074 |
rs767700053 | snp | G/T | 1.64735e-05 | 0.00286993 | missense | ERCC6 | GRCh38.p7 | 10:49532648 | TGAAGCACTCCCTGT[G/T]CCAGCACGTCCTGGT | 2074 |
rs767709344 | snp | A/G/T | 0.000807901 | 0.0200825 | missense | ERCC6 | GRCh38.p7 | 10:49493178 | AACGGAGGCCACCAC[A/G/T]TGTGAAATTCCTTCA | 2074 |
rs767716858 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49470353 | TCTTAGGCTTTTGCT[C/T]TGGTCTCAGATGTTT | 2074 |
rs767725451 | in-del | -/TGACACCTAAGCCGCCCACCC | 1.6522e-05 | 0.00287414 | cds-indel | ERCC6 | GRCh38.p7 | 10:49472973 | TTGCCCCCGTCAGGT[-/TGACACCTAAGCCGCCCACCC]TGACACCTAAGCCGC | 2074 |
rs767754392 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49514252 | ACTCACTCTTCACTA[C/T]ACCCCTGCAAACTTT | 2074 |
rs767770084 | snp | A/T | 1.66302e-05 | 0.00288355 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482891 | AGGAAGCACCTTTTT[A/T]TTAAATTTACCTTTT | 2074 |
rs767788819 | snp | C/T | 6.59033e-05 | 0.00573997 | missense | ERCC6 | GRCh38.p7 | 10:49470700 | TTCAAAGGATCACTT[C/T]GATTAGAAGTTACTG | 2074 |
rs767860936 | snp | A/G | 1.68182e-05 | 0.00289979 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515368 | CGGAACACTTCACAT[A/G]TAAGGCAACATCACA | 2074 |
rs767885298 | snp | C/T | 1.81292e-05 | 0.0030107 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515294 | ACTGTACATAATGTA[C/T]AAAACTATGTTTCTT | 2074 |
rs767904939 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476841 | AACCCTCCCTCCTTC[A/G]CAAAGTCCACCACCG | 2074 |
rs767907732 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533395 | GCATAGGAACAGCGA[C/T]GTTAGGAAAGAGCTT | 2074 |
rs767956069 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | ERCC6 | GRCh38.p7 | 10:49470274 | TGCTTCTGGTAACGC[C/T]TTTTCTTCACCAGGT | 2074 |
rs767987714 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499522 | CTGTAAAGGTTATCT[C/T]CAAATCATATATAGG | 2074 |
rs767992654 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490076 | ACTTTTATTAAATGC[A/G]ATTTCAAGTGACCAT | 2074 |
rs767997161 | snp | A/G/T | 0.000249044 | 0.0111565 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49471114 | CAAAAACTGCTTGAA[A/G/T]ATTTGTCTAAAAAAA | 2074 |
rs768003524 | in-del | -/A | 1.65075e-05 | 0.00287289 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470965 | AAATTAAATGATTTT[-/A]ATGTAATACCTGCAA | 2074 |
rs768017892 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512469 | CATTTCTTCCCAATA[C/T]TGATACTGTACTTAT | 2074 |
rs768044521 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480220 | GAGTCATCCCTTCTC[C/T]GAGAAGCCTTTCTGA | 2074 |
rs768056530 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497635 | TGCTGGACCACAGCA[C/G]GACAATCAACTCCAT | 2074 |
rs768070674 | snp | G/T | 1.68852e-05 | 0.00290557 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474289 | ATGACCCCATGTAAA[G/T]TAAGATTCCCTAGGC | 2074 |
rs768080293 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502694 | GTTCTCAGCCAGGGG[C/T]AATTCTTCTCCCTAT | 2074 |
rs768119446 | snp | C/T | 1.64887e-05 | 0.00287125 | missense | ERCC6 | GRCh38.p7 | 10:49472394 | TGGTAGATCTTTTCT[C/T]CAATGGTGCCCGCAG | 2074 |
rs768120212 | snp | A/G | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525196 | TTAAATTCAAGAGAC[A/G]GTAAAACCAAAAACA | 2074 |
rs768156907 | snp | A/C | 1.65086e-05 | 0.00287298 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532540 | AAGATGGGCTGCACT[A/C]ACGTGAGGTCATCCA | 2074 |
rs768158334 | snp | C/T | 8.30227e-05 | 0.0064424 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476207 | CCAGCTTCTATTTTT[C/T]AGCTGACCTGCATCT | 2074 |
rs768188064 | snp | C/G/T | 3.29925e-05 | 0.00406145 | synonymous-codon, missense | ERCC6 | GRCh38.p7 | 10:49493161 | GTAGAATTGCCACTC[C/G/T]GAACGGAGGCCACCA | 2074 |
rs768212364 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536637 | GTACAAGAGAAAAGG[C/G]AGTTGACAGGGAACA | 2074 |
rs768226710 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535249 | TGGCAAGCAGCTTAC[A/C]TGTAATCAGTACCAT | 2074 |
rs768227510 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479083 | GTAATGGAGCACGGC[C/T]ACATGAGATGAGTAC | 2074 |
rs768273370 | snp | C/T | 3.29723e-05 | 0.00406018 | missense | ERCC6 | GRCh38.p7 | 10:49482850 | GACAGAATGATCCGA[C/T]GAGGGGTGCGAAACT | 2074 |
rs768296886 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524199 | TCTTCTGCCGTTTCC[C/T]GCCCTTGGGCAGAGG | 2074 |
rs768301659 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516873 | GAGTCATCTTTAGGT[A/G]CGTATGAGGGATCAT | 2074 |
rs768326383 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502067 | GTTTTGTTGTTTTGC[C/T]GTCCAAATACTTACT | 2074 |
rs768335148 | snp | A/C | 1.90489e-05 | 0.00308611 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488234 | TCAAGAGACCAATCC[A/C]TCCTAGAGGGCAAAC | 2074 |
rs768367162 | snp | C/T | 6.61004e-05 | 0.00574855 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49506009 | TCTCAGTTTATTCCA[C/T]CTCCTACCATGAAAA | 2074 |
rs768486648 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | ERCC6 | GRCh38.p7 | 10:49470653 | CAAGCCTATCATTGC[C/T]AGTTACATTACTACT | 2074 |
rs768500779 | snp | A/T | 1.66043e-05 | 0.00288129 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528369 | CACTGACTACAGGCA[A/T]CAGGCATCAATTCAA | 2074 |
rs768505023 | snp | A/C | 1.65773e-05 | 0.00287895 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500704 | GCTGGTACCTATGAC[A/C]ACAAACACCAACAAG | 2074 |
rs768525994 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468968 | TAATACCCCTACTAA[A/T]GGATTACAGTCATGG | 2074 |
rs768587285 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513560 | ATTGACTCACAATTC[A/G]GCACGGCTGGGAGGC | 2074 |
rs768589918 | snp | C/T | 3.29489e-05 | 0.00405874 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524616 | CTGCCAAATACTTTT[C/T]GAAGCCTGATGCTTC | 2074 |
rs768608345 | snp | C/T | 1.65589e-05 | 0.00287736 | splice-acceptor-variant | ERCC6 | GRCh38.p7 | 10:49500698 | CTGTCTGCTGGTACC[C/T]ATGACAACAAACACC | 2074 |
rs768680674 | snp | C/T | 3.29489e-05 | 0.00405874 | missense | ERCC6 | GRCh38.p7 | 10:49470233 | CATTGCTCTGTTCCT[C/T]GGCCTCACTCTTGTT | 2074 |
rs768691970 | snp | C/G | 1.65132e-05 | 0.00287339 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472359 | CACAGCCAAGAGTGG[C/G]CACTGTGTGCACTGA | 2074 |
rs768703271 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509516 | CCATAGGAGTAAAGA[C/T]ACCTAGTCTTCAGAT | 2074 |
rs768762049 | snp | A/G | 3.31862e-05 | 0.00407333 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516311 | CATGAATTCATCAAA[A/G]CTGAAATATGTTTCA | 2074 |
rs768790538 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531786 | CCTCCCCAGCTATCC[A/T]CTGTGACACTGCTCC | 2074 |
rs768802039 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531004 | CACAAATAAAACTTG[C/T]AGGATCATTAGAGGT | 2074 |
rs768810263 | snp | C/T | 1.64893e-05 | 0.0028713 | missense | ERCC6 | GRCh38.p7 | 10:49500584 | TGTAGCTCAGACCTG[C/T]CAAGAAGGCAATTAT | 2074 |
rs768832103 | snp | A/G | 1.65042e-05 | 0.0028726 | missense | ERCC6 | GRCh38.p7 | 10:49461401 | GGCCAGTCCAGGTGG[A/G]AACACCAGACACTGC | 2074 |
rs768844912 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521223 | GTGAATCAATAACAT[G/T]GAGGTAACAAGGACT | 2074 |
rs768900524 | snp | A/C | | | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470810 | CTTCTTGCGTTTTGG[A/C]ACATCATGGTCTGCT | 2074 |
rs768910855 | in-del | -/TTC | 1.65004e-05 | 0.00287227 | intron-variant, cds-indel | ERCC6, PGBD3 | GRCh38.p7 | 10:49515406 | CATCGAAAAGTTGTG[-/TTC]TTATGACATTCAGCG | 2074 |
rs768913965 | snp | A/G | 1.64827e-05 | 0.00287073 | intron-variant, stop-gained | ERCC6, PGBD3 | GRCh38.p7 | 10:49515911 | CTTTGCCATCAATTC[A/G]ATAATCAAATGTGCC | 2074 |
rs768915628 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532824 | GTCACCCACAGAACG[A/G]AAGGAGAGGTACTCC | 2074 |
rs768992020 | snp | A/C | 1.64798e-05 | 0.00287047 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474126 | AGAACGTTTCCAGTA[A/C]CCAAACTGATCTTCT | 2074 |
rs768993757 | snp | C/G | 1.64773e-05 | 0.00287026 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515575 | CACGTCGACGAAACT[C/G]CAGAAAATCCACTGG | 2074 |
rs769012348 | snp | C/T | 6.59141e-05 | 0.00574045 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515490 | CGTGAGTCAATGTTA[C/T]GCTTCTGAGGTCTTC | 2074 |
rs769020754 | in-del | -/CTT | 1.64738e-05 | 0.00286995 | cds-indel, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524106 | GACCTCCTCCTCCTC[-/CTT]CTCCTACAGAAGCAG | 2074 |
rs769047362 | snp | A/C | 4.94629e-05 | 0.00497283 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530857 | TGAAAAATAAGATAA[A/C]TTGTCTATTTTGCAC | 2074 |
rs769069696 | snp | G/T | 1.64781e-05 | 0.00287033 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516719 | GGTGAAGAAATCGTT[G/T]GGTGGTGCTGTAACT | 2074 |
rs769081218 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473436 | CTTTCCCTCCACGTA[C/T]AGCAGCACCACTCAA | 2074 |
rs769081319 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470543 | ATCACCAGATGGCAT[A/G]GAAGTTTTGCCTGTT | 2074 |
rs769086950 | snp | A/G | 1.65031e-05 | 0.00287251 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478513 | TACTATATATGTTTA[A/G]GGAACGCATTTGTTC | 2074 |
rs769116168 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496663 | AACTATAAAAATTAG[A/C]CGGGTATGGTGGTGA | 2074 |
rs769154645 | snp | C/T | | | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515627 | CAATTGCCAAGCATT[C/T]TGTAAGACCAGTTCG | 2074 |
rs769157895 | snp | A/G | 1.65567e-05 | 0.00287716 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524689 | GATCTGGGTACCAAA[A/G]GGTGTCATCTGGCCA | 2074 |
rs769158037 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522526 | CTGGAAATAATAAAT[C/T]GTTTTACAATCTTAA | 2074 |
rs769170940 | snp | C/T | 1.65198e-05 | 0.00287395 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49473011 | CGTGGTCAGAAGAAA[C/T]ACAAATATGGATGTG | 2074 |
rs769194826 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504605 | CCTTTTGCTAGTACA[A/T]CACTGATGGTATTTG | 2074 |
rs769217920 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527050 | AAAAAGAAAACCAGT[A/G]GAGAAGCAGGGATCC | 2074 |
rs769234947 | snp | C/T | 1.65059e-05 | 0.00287275 | missense | ERCC6 | GRCh38.p7 | 10:49472466 | CTCCATGCTCGCTCC[C/T]GGGCCTGCAACAGAG | 2074 |
rs769239598 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538653 | GCTCCAGCATTTTAA[C/T]CGAGATCAAAAAGGA | 2074 |
rs769248497 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517948 | CTTTTACTAAATTCA[G/T]ATTTTGGGAGAGTTT | 2074 |
rs769343568 | snp | C/T | 1.65798e-05 | 0.00287917 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516442 | GCAAATTAGAAAATA[C/T]AGTTTCAAACCGGTC | 2074 |
rs769351934 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491077 | AGATCGAAGGTGCAG[A/C]GGAAGCAAATACCCC | 2074 |
rs769355279 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534390 | ATTCCAGAGAACTAG[C/T]CACACACAGGTGCAA | 2074 |
rs769371302 | snp | C/T | 5.05919e-05 | 0.00502925 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461573 | TAGCAAGAAAAGAAA[C/T]AGCAAAGTGATATTT | 2074 |
rs769421755 | snp | C/T | 1.65056e-05 | 0.00287272 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474020 | CGTCTGAAGTCTGTG[C/T]ACTCACCTGCCTTGA | 2074 |
rs769434036 | snp | C/T | 3.29473e-05 | 0.00405864 | missense | ERCC6 | GRCh38.p7 | 10:49458999 | TGGAAAGCGATGAAG[C/T]TTCTCATCTCCACCA | 2074 |
rs769439823 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503321 | TGTTTCCTCATCTAC[A/G]AATCTAATCTTCGAC | 2074 |
rs769452612 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513267 | CTAACCCCTATGCTA[C/T]ATACTGCCTCCTTAA | 2074 |
rs769480050 | snp | C/T | 1.65559e-05 | 0.00287709 | splice-donor-variant | ERCC6 | GRCh38.p7 | 10:49476214 | CTATTTTTTAGCTGA[C/T]CTGCATCTCTCCATT | 2074 |
rs769491240 | snp | C/G | 1.64749e-05 | 0.00287005 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530713 | ACTGAATGTTATTCT[C/G]AATCACCTTATTATA | 2074 |
rs769513102 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467622 | CCAGGCTGGAGTGCA[A/G]TGGCATGATCACAGC | 2074 |
rs769535842 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49472264 | CCAAAGCCTTAAGTT[A/G]TAGCAACTATTATTC | 2074 |
rs769569676 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511111 | AAGTCTGAGCTCCAT[G/T]TTTTGGGTTCATCAC | 2074 |
rs769589352 | snp | A/T | 0.000263561 | 0.0114765 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516986 | TCCACCTTCTTCATC[A/T]CCTGATTCCTCATCA | 2074 |
rs769590741 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459584 | GACCACTTTCAGTAC[C/T]TGTGGGCTTTTCCTG | 2074 |
rs769594258 | snp | A/C | 1.64844e-05 | 0.00287087 | missense | ERCC6 | GRCh38.p7 | 10:49470414 | ATGTTTTGTTTTTGA[A/C]TTGTGCTTATAAAAA | 2074 |
rs769599897 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480122 | ATGCCCTGCCCCAGC[A/T]GAGCACACCAACCCC | 2074 |
rs769601606 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49466749 | AAAGTCATCCATGCT[A/G]TAGCATGTATCAATA | 2074 |
rs769625730 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454889 | ACATTTCCGTACATT[A/G]TATGTAAATTGGTAA | 2074 |
rs769643280 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488160 | TAGCCTGACTTACTG[A/C]ATGCAGTGCTGTTGT | 2074 |
rs769713609 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523821 | CCTCCAAATCCAACT[A/G]AAGACCTAGAAGTAC | 2074 |
rs769733106 | snp | A/C/T | 0.000132252 | 0.0081308 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49528514 | TGCAGTGATCTTTTT[A/C/T]AGCTGTTGTTCCTTG | 2074 |
rs769745354 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | ERCC6 | GRCh38.p7 | 10:49458868 | CACCAGAAGTTCTAT[A/G]GAAAGTGCACAGATT | 2074 |
rs769746995 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483319 | TCTTCTCCACTTGGA[A/G]ATCTCCCTTGTTAAA | 2074 |
rs769752436 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535112 | CTCAATATCTGCTGA[A/C]AGGAAGTGAGGTTCA | 2074 |
rs769766942 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478809 | TAGAGACTTACTGGG[G/T]TCTTGACCACCAGCC | 2074 |
rs769789271 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521186 | AGCTATGGAGGCTTA[C/T]CTCGAATATGGCAAC | 2074 |
rs769842725 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520249 | CCCACGCTACACTTC[C/T]TAAGTCAGCGTCTCC | 2074 |
rs769843640 | snp | A/G | 1.65236e-05 | 0.00287429 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49473020 | AAGAAACACAAATAT[A/G]GATGTGTCCTAGAGG | 2074 |
rs769850417 | snp | A/T | 1.64757e-05 | 0.00287012 | missense | ERCC6 | GRCh38.p7 | 10:49530783 | TCTGCTGGTGGCAGC[A/T]TGAGGGCTAAGCTGT | 2074 |
rs769858072 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527919 | CTTACGAATTTTCCC[-/A]AAAAGTTTTCCAAAA | 2074 |
rs769893726 | snp | C/T | 1.65455e-05 | 0.00287619 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49505910 | TTTGAACAGAAAACC[C/T]GGCACTTTAAAACCT | 2074 |
rs769894653 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506538 | TTACTGATTACTTAA[C/T]TGGGGGAAGAGGCAT | 2074 |
rs769902302 | snp | C/G | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515338 | GTGACACCTGCTATT[C/G]AGTGTGATATTCAAC | 2074 |
rs769904341 | snp | C/T | 1.64906e-05 | 0.00287142 | missense | ERCC6 | GRCh38.p7 | 10:49482859 | ATCCGATGAGGGGTG[C/T]GAAACTATTTGAGGA | 2074 |
rs769917116 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474776 | GCATGAAAAATGCAC[A/G]AATAGGAATGCACGA | 2074 |
rs769952357 | snp | A/C | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458275 | CCTTGAAAAGAGGAT[A/C]TTTCCAAGAAAATTA | 2074 |
rs769961550 | snp | G/T | 3.55126e-05 | 0.00421367 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524800 | AACAATAGCAATGCG[G/T]TTCGCACTAGCATGA | 2074 |
rs769975274 | snp | A/G | 1.66371e-05 | 0.00288414 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461465 | TTTCAGGGCATCCTG[A/G]GCCACTCGGTTGGCT | 2074 |
rs769990464 | snp | C/G | 1.64779e-05 | 0.00287031 | missense | ERCC6 | GRCh38.p7 | 10:49532934 | CTTGCTCCTGAGTTT[C/G]ACTTGAGTGGGGGAT | 2074 |
rs770008494 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488484 | AATTTTACAACATAC[C/G]TCGCAGAACAAGCCC | 2074 |
rs770021220 | snp | A/C | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455436 | GGAACAGAAAACACC[A/C]AAGTATAAGACACTG | 2074 |
rs770038439 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461085 | ATCATTATCCTGTAT[C/T]TCTTACTATTTTTAA | 2074 |
rs770044811 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481565 | CCATGACCTGGTAGG[C/T]ACAGGCCCACCCAAG | 2074 |
rs770056661 | snp | C/T | 1.66123e-05 | 0.00288199 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524698 | ACCAAAAGGTGTCAT[C/T]TGGCCAGTGCGGATG | 2074 |
rs770088246 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463838 | CTCCTTGCCTTCTGA[C/G]ATGACTGTGAGGCCT | 2074 |
rs770101882 | in-del | -/TTAATG | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481000 | GATAACAGACTCCTA[-/TTAATG]TTAAACTTCGTTCTG | 2074 |
rs770120527 | snp | A/C/T | 4.94257e-05 | 0.004971 | missense | ERCC6 | GRCh38.p7 | 10:49532616 | GGCTGGCCTCATGGA[A/C/T]GGCATTGTCCACCTG | 2074 |
rs770151886 | snp | A/T | 1.64765e-05 | 0.00287019 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515610 | TCATCATATGTTTTA[A/T]GCAATTGCCAAGCAT | 2074 |
rs770164527 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524223 | GCAGAGGCTTCAGCT[C/T]ATAGTCAGTACCATC | 2074 |
rs770165988 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512140 | GTCTTGAGCCAGCAG[G/T]AGCTCAGTTCAACCC | 2074 |
rs770183037 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496268 | ACAAAACACAAATCA[C/T]CTTTACTGTAATTGT | 2074 |
rs770232627 | in-del | -/A | 0.0139671 | 0.0823921 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476344 | GGAAACTATAATTTC[-/A]AAAAAAAAAATTAAC | 2074 |
rs770234264 | snp | A/C | 1.64779e-05 | 0.00287031 | missense | ERCC6 | GRCh38.p7 | 10:49470768 | AGATGATGTGGCATC[A/C]TTTACAGATATGTTA | 2074 |
rs770245335 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508072 | TATCAAAACTATGAA[C/T]GCAGAGCCAAACTTC | 2074 |
rs770261824 | snp | A/C | 1.6477e-05 | 0.00287024 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473443 | TCCACGTACAGCAGC[A/C]CCACTCAACTTCCCT | 2074 |
rs770307740 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49472194 | ATTTTTTGACAACTC[-/A]ACAGTAAGACATCTA | 2074 |
rs770355997 | snp | A/C | 6.77381e-05 | 0.00581932 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515363 | TTCAACGGAACACTT[A/C]ACATGTAAGGCAACA | 2074 |
rs770358962 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537079 | TGCCGGGAGCGGTGG[C/T]TCATGCCTGTAATCC | 2074 |
rs770380323 | snp | A/G | 4.94572e-05 | 0.00497254 | missense | ERCC6 | GRCh38.p7 | 10:49470419 | TTGTTTTTGACTTGT[A/G]CTTATAAAAATTATT | 2074 |
rs770384997 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463100 | CCAGAAGTGCTTCAG[A/T]TTTTGCCTTTTTCAG | 2074 |
rs770391787 | in-del | -/TTTTGT | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540034 | GGGTTTTTTTGTTTG[-/TTTTGT]TTTTGTTTTTGTTTT | 2074 |
rs770443998 | snp | A/T | 6.61967e-05 | 0.00575273 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516465 | AACCGGTCACGTCTC[A/T]TGGCAGCACTAACCA | 2074 |
rs770450629 | snp | G/T | 1.64749e-05 | 0.00287005 | missense | ERCC6 | GRCh38.p7 | 10:49530725 | TCTGAATCACCTTAT[G/T]ATACTTCTGTCGTTT | 2074 |
rs770460188 | snp | C/T | 3.41e-05 | 0.00412902 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472912 | ATAAAAACAAACCTG[C/T]GTGTCCGTGCTTGGG | 2074 |
rs770464886 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515456 | CTGTTTGACTATCAC[A/G]TGATTTATGCCATCA | 2074 |
rs770483383 | snp | C/T | 1.65007e-05 | 0.00287229 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516604 | TCAAGCCAAGATGTA[C/T]ACCTTTACTGCAAGC | 2074 |
rs770537477 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520872 | GCCTCCAAAGCAAAG[C/T]AAATTCCTTCCCTTC | 2074 |
rs770541513 | snp | C/T | 8.23662e-05 | 0.00641688 | missense | ERCC6 | GRCh38.p7 | 10:49470328 | TTGGCGTCTCTGCAA[C/T]GCTTAGAGTTCTTAG | 2074 |
rs770553083 | snp | A/T | 1.64751e-05 | 0.00287007 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483331 | GGAAATCTCCCTTGT[A/T]AAAAGAGGTCATACC | 2074 |
rs770556238 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49478416 | TCATTCTCCGCAGTA[A/G]GTATGGATTTATGGT | 2074 |
rs770620107 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512161 | AGTTCAACCCCCAAG[-/C]ATAGCAGACTGTCAT | 2074 |
rs770629263 | snp | C/G | 3.30256e-05 | 0.00406346 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472473 | CTCGCTCCCGGGCCT[C/G]CAACAGAGAGAGAGA | 2074 |
rs770659811 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527614 | CGGGAGGCAGAGGTT[G/T]CAGTGAGCTGAGATG | 2074 |
rs770673858 | in-del | -/CCTA | 1.65293e-05 | 0.00287479 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506012 | CAGTTTATTCCATCT[-/CCTA]CCATGAAAATAAAAA | 2074 |
rs770687933 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465174 | CACCTCTTGCATCAG[C/T]GTGACCTGGATGCGA | 2074 |
rs770711353 | snp | A/G | 1.66225e-05 | 0.00288287 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516074 | ATTGAATACAAAATG[A/G]TATTGTCCAGGGTGT | 2074 |
rs770727532 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492349 | AGCTCCTAAGAGACT[A/G]CTGCTTCTCCCCAAT | 2074 |
rs770732269 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49530816 | AATAATTTTATTGAT[C/T]TGCCTTAGGGATGTC | 2074 |
rs770769700 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49532210 | GCAATGTATTCCTGG[A/C]ATCTCGAATAGGAAA | 2074 |
rs770779441 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477329 | AGGATGGAGGGCAAC[C/G]CTTCCACCTCTGCAC | 2074 |
rs770782370 | snp | A/G | 3.34253e-05 | 0.00408797 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474262 | GGTAAGAAAGAGTAC[A/G]TGTACACTCAGATGA | 2074 |
rs770843243 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534269 | AGGATCCCCCCTCAC[A/G]TAGTGCTGCTGAGAA | 2074 |
rs770862651 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459010 | GAAGTTTCTCATCTC[C/T]ACCAGAAGGTCATCG | 2074 |
rs770918391 | in-del | -/G | 1.66493e-05 | 0.0028852 | frameshift-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524300 | TCTTCCTCCTCCTCT[-/G]TGGGGAAATACTCAG | 2074 |
rs770937435 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521341 | GCTGCACAGCCTGTA[C/T]TAGGTAAGCAGCATG | 2074 |
rs770970738 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49530637 | TCACATCTTATAAGC[A/G]CTTTTTAAAATACTT | 2074 |
rs771003061 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460341 | AATCAAGCAAGTCTC[A/C]CCCTGGAAAGCAAAA | 2074 |
rs771016726 | snp | C/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518014 | GCACAATCAAATCAA[C/G]CTCCACATTGTGAGT | 2074 |
rs771026985 | snp | A/C | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455792 | ATGTTTGATTTTGTA[A/C]GTAATCAGGGAAATT | 2074 |
rs771037314 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486447 | ATAAAAATTAGTGGG[C/T]ATTAAAAAAACTGGT | 2074 |
rs771037718 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476093 | ACCATGCGGGACTTC[A/G]TGCAAGTGAAGTGAG | 2074 |
rs771053669 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511720 | GTGAGCCACCATTCC[C/T]GACCCATCAGGGCAT | 2074 |
rs771060467 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529495 | GCACATCAATTTCAC[A/G]TGCTCCCACAAGAGA | 2074 |
rs771112249 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49466582 | CAATCAAGACAATGA[A/T]CATAGCCGTCACCTG | 2074 |
rs771141559 | snp | A/T | 1.799e-05 | 0.00299911 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524813 | CGTTTCGCACTAGCA[A/T]GAAACTTTCCGAGGG | 2074 |
rs771221191 | snp | A/G | 1.65121e-05 | 0.00287329 | stop-gained | ERCC6 | GRCh38.p7 | 10:49505990 | GTTTCTCTTTGTCCT[A/G]CAGTCTCAGTTTATT | 2074 |
rs771239993 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511782 | AGTGGTGGTCACTAG[A/G]AGAGAACCCAACAAC | 2074 |
rs771247321 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535464 | TCCTTCTTTTGGGGC[C/G]TGCTGATTATTTTCA | 2074 |
rs771248482 | in-del | -/TA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537488 | CAGACATTTAAAAAC[-/TA]TATATATATATATAC | 2074 |
rs771252681 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524476 | TTTGGACAGAACTCT[A/G]GCTTTCTTGTTTGGT | 2074 |
rs771290763 | snp | C/G | 3.32372e-05 | 0.00407646 | splice-donor-variant | ERCC6 | GRCh38.p7 | 10:49461351 | TGCAGCAATCTCTTA[C/G]TTTTTTCCTGCTGGT | 2074 |
rs771292182 | in-del | -/AC | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49466515 | AATAACTGCTAAAGT[-/AC]ACAGTATTTGGTAAG | 2074 |
rs771311272 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507642 | TACAACAATCGTTCT[C/T]GACAGGGGGCAATTC | 2074 |
rs771313924 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474665 | CATTTAAATATTACA[C/T]TCCTAATTACCTCAC | 2074 |
rs771314919 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535282 | GCAGCATGCAGTCAG[A/T]AATGCAAATCTGAGC | 2074 |
rs771340868 | snp | G/T | 1.66788e-05 | 0.00288775 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524302 | TTCCTCCTCCTCTGT[G/T]GGGAAATACTCAGAC | 2074 |
rs771402578 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508326 | CATTTCCTTAGACTT[A/T]GCCAGTCAATCTTTG | 2074 |
rs771405607 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49493915 | TGGGAAGCCCACACC[A/G]ACAGTGTACAAGCTG | 2074 |
rs771414850 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469301 | AAAATCAACTTGTAA[C/T]AGGTCAAACCAGCAT | 2074 |
rs771424857 | snp | A/G | 3.30033e-05 | 0.00406209 | missense | ERCC6 | GRCh38.p7 | 10:49474170 | CAGGAAGACCTTTGA[A/G]ATTCTTGGGACCTCC | 2074 |
rs771450153 | snp | A/G/T | 3.30247e-05 | 0.00406343 | missense, synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470854 | GAATCCTTCTTTTTA[A/G/T]ATGGCATTTGGGTGT | 2074 |
rs771454918 | snp | A/T | 3.31989e-05 | 0.00407411 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493258 | CCCCTCAAACCTGCA[A/T]CCAAACGTCCAAGAA | 2074 |
rs771513022 | snp | C/T | 1.64993e-05 | 0.00287218 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483534 | GAGACCACAATAAAA[C/T]GGTAAAGTCAGTTTT | 2074 |
rs771531733 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538093 | TGAGTTAAGAAGAGC[A/T]GAGAAGGGCTCCGTT | 2074 |
rs771532766 | snp | C/G | 4.94287e-05 | 0.00497111 | missense | ERCC6 | GRCh38.p7 | 10:49459113 | ATCAGGTGGTTTCTA[C/G]CTCTCATTTTAGCCA | 2074 |
rs771545049 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500908 | AATTTTTCTTTACAA[A/C]ACATTAACACATTTC | 2074 |
rs771598094 | snp | A/G/T | 0.000510717 | 0.015972 | intron-variant, synonymous-codon, stop-gained | ERCC6, PGBD3 | GRCh38.p7 | 10:49515566 | GGCATACCACACGTC[A/G/T]ACGAAACTCCAGAAA | 2074 |
rs771604820 | snp | C/T | 1.64898e-05 | 0.00287135 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470507 | TTTGTAAGAAAGACC[C/T]AACTTTTCATCAATG | 2074 |
rs771641139 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513727 | CAGCATGGGGGAAAC[C/T]GCCCCCATAATCCAA | 2074 |
rs771681534 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524047 | CCTTAACCGCTGCTT[A/G]TAATAATCTTCATCT | 2074 |
rs771692143 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | ERCC6 | GRCh38.p7 | 10:49459036 | CATCGTGTTCTGTGG[C/T]GGGCAGCAGGGCAGA | 2074 |
rs771726585 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481456 | ATTGTTTTTGACAAT[C/G]TTTTAATCTTAAAGG | 2074 |
rs771739674 | snp | C/T | 6.671e-05 | 0.00577499 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524708 | GTCATCTGGCCAGTG[C/T]GGATGAGCTCTTCCC | 2074 |
rs771748055 | snp | C/T | 1.65362e-05 | 0.00287538 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49505925 | TGGCACTTTAAAACC[C/T]TCGTCAAATTCAGCA | 2074 |
rs771764451 | snp | C/T | 1.66596e-05 | 0.00288609 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516174 | TTTGGGTTTTTACCC[C/T]GATACGGCTGAAACC | 2074 |
rs771781694 | snp | A/G | 4.94238e-05 | 0.00497086 | stop-gained | ERCC6 | GRCh38.p7 | 10:49530737 | TATTATACTTCTGTC[A/G]TTTTACAGAATCTAG | 2074 |
rs771825594 | snp | G/T | 1.64879e-05 | 0.00287118 | missense | ERCC6 | GRCh38.p7 | 10:49532949 | GACTTGAGTGGGGGA[G/T]TCCCTCATTTGGCAT | 2074 |
rs771828895 | in-del | -/A | 1.66504e-05 | 0.0028853 | splice-acceptor-variant | ERCC6 | GRCh38.p7 | 10:49471122 | CTTGAAGATTTGTCT[-/A]AAAAAAATAAAAGAT | 2074 |
rs771890159 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495093 | TGTCCCTTTTCTTGT[C/T]TGAGACCAATCCCTT | 2074 |
rs771890251 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480358 | TGGAAATACCTTCAT[G/T]GGAAGGTTCTGGTTT | 2074 |
rs771907799 | snp | G/T | 0.00805882 | 0.062964 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505847 | TGTACATAATGGCTT[G/T]ATAGCAAATAGAAAG | 2074 |
rs771954625 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500066 | AATGGCTTCTTCAAA[A/G]CTCCAACTCTCCCCA | 2074 |
rs771999892 | snp | C/T | 1.66416e-05 | 0.00288453 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516101 | GTGTGCCTCTGTAAG[C/T]GCCTCACTAAACTGA | 2074 |
rs772019940 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532737 | CTGGATCTGATGTCG[A/G]TCGATGTGCAGCAGG | 2074 |
rs772030276 | snp | A/G | 3.29663e-05 | 0.00405981 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515870 | AGTGACAACACTGTT[A/G]TCATTCCATCTGCAG | 2074 |
rs772047558 | snp | C/T | | | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532902 | ATTATTACTGACAGG[C/T]TGACTCTGTAAACAG | 2074 |
rs772090380 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524175 | CATCAATCTCCTGCA[C/T]TGGCACTTTCTTCTG | 2074 |
rs772094804 | snp | C/T | 1.65181e-05 | 0.00287381 | missense | ERCC6 | GRCh38.p7 | 10:49470862 | CTTTTTAGATGGCAT[C/T]TGGGTGTCTGAACAT | 2074 |
rs772100335 | snp | C/T | | | missense | ERCC6 | GRCh38.p7 | 10:49470542 | CATCACCAGATGGCA[C/T]AGAAGTTTTGCCTGT | 2074 |
rs772103097 | in-del | -/TCA | 3.29533e-05 | 0.00405901 | intron-variant, cds-indel | ERCC6, PGBD3 | GRCh38.p7 | 10:49515595 | AAATCCACTGGTTTC[-/TCA]TCATATGTTTTATGC | 2074 |
rs772104945 | snp | C/G | 1.64879e-05 | 0.00287118 | missense | ERCC6 | GRCh38.p7 | 10:49471071 | TGAAAAACCGCCTTT[C/G]TTTTGGGTCTTTTAG | 2074 |
rs772112460 | snp | A/C | 0.00016778 | 0.0091576 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474278 | TGTACACTCAGATGA[A/C]CCCATGTAAAGTAAG | 2074 |
rs772175863 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498029 | ATAAGATTGAGGGGC[C/T]TATCATTATAATATG | 2074 |
rs772193885 | snp | A/T | 1.64917e-05 | 0.00287151 | intron-variant, stop-gained | ERCC6, PGBD3 | GRCh38.p7 | 10:49515797 | TCTTCTTTTTCAGTT[A/T]CTGGGAGTAACGACT | 2074 |
rs772193950 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510806 | CAAATGGGGTCATCC[A/G]GAAATGGGTTCTGGA | 2074 |
rs772236323 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479986 | CTGACAAGGCAGAGC[C/T]CTGCCTCTTCCTGAG | 2074 |
rs772242929 | snp | A/T | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539141 | GCGCCTGGCTCAGCG[A/T]TTGTTTTTAAGCACG | 2074 |
rs772254660 | snp | G/T | 3.29565e-05 | 0.00405921 | missense | ERCC6 | GRCh38.p7 | 10:49470782 | CATTTACAGATATGT[G/T]AGAAGCAGGGAACTT | 2074 |
rs772285870 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516968 | TGGCAGATTATTTAT[C/T]GTTCCACCTTCTTCA | 2074 |
rs772292388 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529453 | CCCTTGAAATTCCAG[-/C]CCCACTAGAAGCCCA | 2074 |
rs772306982 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465087 | CACTCAATGCCACCC[A/G]TGAAAGCAGCCAGGA | 2074 |
rs772344335 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49473566 | TTTGGGCTCTAAGGA[A/G]TACTTCAAGTATGTC | 2074 |
rs772374457 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522046 | CCTCAGTAAAAGGTG[G/T]TAAGTTCAGCAAAGG | 2074 |
rs772397742 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529211 | TTCCAAGGTCAAGAA[C/T]GTTTCAACTTCAAAT | 2074 |
rs772402467 | snp | A/C | 6.60153e-05 | 0.00574485 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483305 | TCTGAATTAATTATT[A/C]TTCTCCACTTGGAAA | 2074 |
rs772414079 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524502 | TTGGTTTGTTTTTAT[C/T]TTGCACTGGGGCTGG | 2074 |
rs772426762 | snp | C/T | 1.6483e-05 | 0.00287076 | missense | ERCC6 | GRCh38.p7 | 10:49458844 | GCTTGAGTTTCCAAA[C/T]TCCTTCACCACCAGA | 2074 |
rs772435867 | snp | C/G | 1.65405e-05 | 0.00287576 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516479 | CATGGCAGCACTAAC[C/G]AGTACATTATGCACA | 2074 |
rs772444165 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485968 | CTGAAAGTTGTAATA[C/T]GGGAATTATCAAAGA | 2074 |
rs772464804 | snp | C/T | 1.65132e-05 | 0.00287339 | missense | ERCC6 | GRCh38.p7 | 10:49461383 | CACCAGAAATCCCCC[C/T]GTGGCCAGTCCAGGT | 2074 |
rs772517211 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469349 | CACTGAGTAAGATAC[A/G]GTATCACCTCTGTGG | 2074 |
rs772545860 | in-del | -/TGA | 1.64781e-05 | 0.00287033 | cds-indel, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524218 | TTGGGCAGAGGCTTC[-/TGA]AGCTCATAGTCAGTA | 2074 |
rs772546662 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504850 | TAGAGTTTGGCTTTC[G/T]ATAATGTTTAGTGGG | 2074 |
rs772596880 | snp | A/C | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540060 | TTTTTGTTTTTGAGA[A/C]GGAGTTTTGCTCTTG | 2074 |
rs772628306 | snp | A/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517895 | GTTAAGAACATTCTT[A/T]AAATAATTGTATTTA | 2074 |
rs772633733 | snp | A/G | | | missense | ERCC6 | GRCh38.p7 | 10:49532901 | CATTATTACTGACAG[A/G]TTGACTCTGTAAACA | 2074 |
rs772646937 | snp | A/T | | | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516857 | TGGAACTTCATCAGG[A/T]GAGTCATCTTTAGGT | 2074 |
rs772713214 | snp | A/G | 4.95217e-05 | 0.00497578 | missense | ERCC6 | GRCh38.p7 | 10:49472467 | TCCATGCTCGCTCCC[A/G]GGCCTGCAACAGAGA | 2074 |
rs772733062 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457704 | AAATTTCAGGAATAC[A/G]ATGAATTTCGGAAAA | 2074 |
rs772746536 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525524 | CCAGAAAGTATCCCT[C/T]TTTCATTAGTTGAAA | 2074 |
rs772752006 | snp | A/G | | | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515204 | GAACAAAAATTTGAA[A/G]AGAAAAAAAAATTTA | 2074 |
rs772769220 | snp | A/G | 1.65726e-05 | 0.00287855 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516213 | TAGCCCAGACAGGTG[A/G]CACCACACCAAAACT | 2074 |
rs772770938 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495112 | GACCAATCCCTTTAG[C/G]TAAGCTCTTGAGCTT | 2074 |
rs772801089 | snp | A/G | 4.94907e-05 | 0.00497422 | stop-gained | ERCC6 | GRCh38.p7 | 10:49472377 | CTGTGTGCACTGACC[A/G]GTGGTAGATCTTTTC | 2074 |
rs772831369 | snp | C/T | 3.31362e-05 | 0.00407026 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516274 | TAAATTGTTTGCACC[C/T]GTGACGACCAAAATA | 2074 |
rs772846743 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508500 | CATTCTAGTGCCTTC[C/T]GCTTCATAAAGAAAG | 2074 |
rs772880581 | snp | A/G | 1.67899e-05 | 0.00289736 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476315 | CAAAATAAGACCTAC[A/G]GACGGGAAAAACAAG | 2074 |
rs772890137 | snp | A/G | 6.62691e-05 | 0.00575588 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506041 | AAAAATCACATTTCC[A/G]TTATTTTGATCACAA | 2074 |
rs772933396 | in-del | -/T | 1.66558e-05 | 0.00288577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476201 | TTTCTCCAGCTTCTA[-/T]TTTTTTAGCTGACCT | 2074 |
rs772952335 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489798 | CTAAAGATGTCACCA[C/T]CTACTGTGAGTTATG | 2074 |
rs772960415 | snp | C/G | 1.64784e-05 | 0.00287035 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473608 | TGGAGGTGGGGGATA[C/G]GAGTTTGCAAAGCAA | 2074 |
rs773039517 | snp | C/T | 3.35706e-05 | 0.00409685 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517107 | TGTAAACTTAGTGTT[C/T]GAGGCATCTTGGGAC | 2074 |
rs773056239 | in-del | -/AC | 1.65121e-05 | 0.00287329 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472476 | GCTCCCGGGCCTGCA[-/AC]AGAGAGAGAGAGACC | 2074 |
rs773083950 | snp | A/C/G | 3.29464e-05 | 0.00405861 | missense | ERCC6 | GRCh38.p7 | 10:49459005 | GCGATGAAGTTTCTC[A/C/G]TCTCCACCAGAAGGT | 2074 |
rs773105266 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521306 | ATGTTTGGTCTTCTG[G/T]GCCACACAGGGCTGT | 2074 |
rs773109178 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464187 | GTCTCAGACGGAGAT[A/G]AGGAACTTGTTGGGA | 2074 |
rs773111961 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462903 | GAGTTGGGCATTATT[C/G]AAACAAACAAACAAA | 2074 |
rs773113703 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528175 | CAGTGTATTAAATGT[A/G]ATAATAAATGTGTAC | 2074 |
rs773119083 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517005 | GATTCCTCATCAGAA[A/G]CAGGTGCTGTAGCAT | 2074 |
rs773120316 | snp | C/T | 4.94907e-05 | 0.00497422 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474030 | CTGTGCACTCACCTG[C/T]CTTGACTGAGAAAAC | 2074 |
rs773177478 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528245 | TTCTCTTTGAGAGGG[-/A]TTTGGTTCTGCAGGT | 2074 |
rs773184770 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498425 | GAACTCCCAAGTTCA[C/T]CTGGTTCCAGAGGAG | 2074 |
rs773209953 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498068 | AGTGAAAAGAAGGTG[G/T]TGTATCCATTATGAA | 2074 |
rs773221500 | snp | C/T | 4.94262e-05 | 0.00497098 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483327 | ACTTGGAAATCTCCC[C/T]TGTTAAAAGAGGTCA | 2074 |
rs773245940 | in-del | -/T | 1.64773e-05 | 0.00287026 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49515721 | TGTTTTCATCAGCTC[-/T]TGTCTACGCCTCCCA | 2074 |
rs773275505 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500101 | TAGACTTTGTACTTA[C/T]TGTAATGCTCACCTG | 2074 |
rs773298508 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510835 | GAAACTTTCTGTTCT[C/G]TCTCATTTAGAGCCT | 2074 |
rs773346976 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531894 | GCAGCAATGATAAGT[A/G]AGCTCAACCCCTCCC | 2074 |
rs773358518 | snp | C/T | 1.65157e-05 | 0.0028736 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478520 | TATGTTTAAGGAACG[C/T]ATTTGTTCTTACCTC | 2074 |
rs773391497 | snp | G/T | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539158 | TGTTTTTAAGCACGG[G/T]CAAGACCACGTGGTT | 2074 |
rs773446494 | snp | A/C | 1.66007e-05 | 0.00288098 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500716 | GACAACAAACACCAA[A/C]AAGAAAAGAGAAAAT | 2074 |
rs773476655 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496760 | TTGCAGTGAGCTGAG[A/G]TTGTGCCACTGCACT | 2074 |
rs773477196 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538752 | GGGACTCAAGCCGCC[C/T]CAGGTGAGCGCTCCT | 2074 |
rs773493028 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509864 | CTCATTTTAAAAAAT[C/T]CACACACGTAATAGT | 2074 |
rs773498737 | snp | A/G | 3.2963e-05 | 0.00405961 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524226 | GAGGCTTCAGCTCAT[A/G]GTCAGTACCATCTCC | 2074 |
rs773516420 | snp | C/G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465109 | CAGCCAGGAGGGGGG[C/G/T]TATACCCTGCAAAGC | 2074 |
rs773516931 | snp | A/G | 1.64936e-05 | 0.00287168 | missense | ERCC6 | GRCh38.p7 | 10:49493173 | CTCTGAACGGAGGCC[A/G]CCACGTGTGAAATTC | 2074 |
rs773537663 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515691 | TTTCCACGGATTGAT[A/G]CCCGATACTTATCAA | 2074 |
rs773544808 | snp | C/T | 1.65414e-05 | 0.00287583 | missense | ERCC6 | GRCh38.p7 | 10:49476218 | TTTTTAGCTGACCTG[C/T]ATCTCTCCATTGAGA | 2074 |
rs773561749 | snp | C/T | 1.66134e-05 | 0.00288208 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524699 | CCAAAAGGTGTCATC[C/T]GGCCAGTGCGGATGA | 2074 |
rs773581901 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524622 | AATACTTTTCGAAGC[C/T]TGATGCTTCATTAAG | 2074 |
rs773630439 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473445 | CACGTACAGCAGCAC[C/T]ACTCAACTTCCCTGT | 2074 |
rs773632137 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460754 | GGTGAAATCCCGTCT[C/G]TACTAAAAATACAAA | 2074 |
rs773636669 | snp | A/T | 0.000743356 | 0.0192646 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475413 | TCCTGGATAGTGTGA[A/T]CTAGACCCCCTAACT | 2074 |
rs773706080 | snp | C/T | 3.29815e-05 | 0.00406075 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532560 | GAGGTCATCCAGGAC[C/T]GACCGATACTCCTTC | 2074 |
rs773708875 | snp | A/G | 1.65392e-05 | 0.00287564 | missense | ERCC6 | GRCh38.p7 | 10:49460402 | TTGGAGATGTTGATG[A/G]AGGATGCTGCACAGA | 2074 |
rs773713355 | snp | A/G | 1.64917e-05 | 0.00287151 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483525 | GTTTCTCCTGAGACC[A/G]CAATAAAATGGTAAA | 2074 |
rs773727974 | snp | G/T | 1.64765e-05 | 0.00287019 | missense | ERCC6 | GRCh38.p7 | 10:49470672 | TACATTACTACTCAT[G/T]TGAGGGTCATCTTTC | 2074 |
rs773769291 | in-del | -/TCTTCCTCCTCT | 1.65899e-05 | 0.00288005 | cds-indel | ERCC6 | GRCh38.p7 | 10:49524276 | CCCTCCACCTCGTCA[-/TCTTCCTCCTCT]TCCTCCTCCTCTGTG | 2074 |
rs773790972 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467100 | TAGTATTTGATCATA[C/T]GGATATGCCATGGTT | 2074 |
rs773801564 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515623 | TATGCAATTGCCAAG[C/T]ATTTTGTAAGACCAG | 2074 |
rs773809609 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479122 | CGCAAAAAAAAAAAG[C/T]CCCACAGCCCAGAAA | 2074 |
rs773819856 | in-del | -/T | 1.64762e-05 | 0.00287016 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49459117 | GGTGGTTTCTAGCTC[-/T]CATTTTAGCCAAGAG | 2074 |
rs773833641 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463803 | TGCCTGCTGCCGTCC[A/C]TGTAAGATGTGACTT | 2074 |
rs773851299 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | ERCC6 | GRCh38.p7 | 10:49459024 | CCACCAGAAGGTCAT[C/T]GTGTTCTGTGGTGGG | 2074 |
rs773865593 | snp | C/T | 1.6486e-05 | 0.00287102 | missense | ERCC6 | GRCh38.p7 | 10:49470422 | TTTTTGACTTGTGCT[C/T]ATAAAAATTATTTTC | 2074 |
rs773881242 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467862 | GCTGAGCCACCACAC[A/C]CAGCCAGTAATTTTT | 2074 |
rs773909779 | snp | A/G | 1.81529e-05 | 0.00301266 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515282 | AACCACTGCTACACT[A/G]TACATAATGTATAAA | 2074 |
rs773942113 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535277 | CATTTGCAGCATGCA[A/G]TCAGAAATGCAAATC | 2074 |
rs773944918 | in-del | -/G | 3.29739e-05 | 0.00406028 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49470986 | ATACCTGCAAAAATT[-/G]CACTTGTTTCAGTGC | 2074 |
rs773955400 | snp | A/C/G | 3.29473e-05 | 0.00405864 | missense | ERCC6 | GRCh38.p7 | 10:49470334 | TCTCTGCAATGCTTA[A/C/G]AGTTCTTAGGCTTTT | 2074 |
rs773967510 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480222 | GTCATCCCTTCTCCG[A/G]GAAGCCTTTCTGAGC | 2074 |
rs773976648 | snp | A/G | 3.29772e-05 | 0.00406048 | missense | ERCC6 | GRCh38.p7 | 10:49474040 | ACCTGCCTTGACTGA[A/G]AAAACAGCAATACTC | 2074 |
rs774000889 | snp | A/G | 1.68562e-05 | 0.00290307 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515366 | AACGGAACACTTCAC[A/G]TGTAAGGCAACATCA | 2074 |
rs774023569 | snp | C/T | 0.000203118 | 0.0100756 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528541 | CTTGAATGGTAAATA[C/T]AGAAGACAGAAAACA | 2074 |
rs774154361 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | ERCC6 | GRCh38.p7 | 10:49532832 | CAGAACGAAAGGAGA[A/G]GTACTCCTCCACCTC | 2074 |
rs774154865 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495687 | CCCACTGTCCAGGTG[C/T]CCAAATCAGAAACCT | 2074 |
rs774155003 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49500739 | GAGAAAATGGCAAAT[A/G]GTGGATAATACAGAT | 2074 |
rs774162789 | snp | C/T | 1.72537e-05 | 0.0029371 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517128 | ATCTTGGGACTAAAA[C/T]GGAAAAAAGGTATTA | 2074 |
rs774175886 | snp | A/C | 0.000131957 | 0.00812163 | missense | ERCC6 | GRCh38.p7 | 10:49500616 | TGGATGGTCTTGCCC[A/C]ATCCCATTTCATCTC | 2074 |
rs774185021 | snp | C/G | 1.66454e-05 | 0.00288486 | missense | ERCC6 | GRCh38.p7 | 10:49461467 | TCAGGGCATCCTGGG[C/G]CACTCGGTTGGCTTC | 2074 |
rs774205664 | in-del | -/TAGA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503972 | ATTTGACTGCTAAAT[-/TAGA]TAGACAAATATACTT | 2074 |
rs774230628 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461568 | CCAACTAGCAAGAAA[A/G]GAAATAGCAAAGTGA | 2074 |
rs774234731 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538690 | TGACCCTGCGCGCAG[G/T]GGGCCTTATACAAAG | 2074 |
rs774245903 | snp | C/T | 6.65082e-05 | 0.00576625 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516078 | AATACAAAATGGTAT[C/T]GTCCAGGGTGTGCCT | 2074 |
rs774251214 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456178 | GTATTTTATTTTACT[C/T]TTAAATAACAGGTCA | 2074 |
rs774259621 | snp | A/G | 1.64852e-05 | 0.00287094 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515955 | TTTAAAGCTACATCT[A/G]ATTCCAGTGGAACTC | 2074 |
rs774293345 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | ERCC6 | GRCh38.p7 | 10:49470999 | TTGCACTTGTTTCAG[C/T]GCTCTGGGATGCATC | 2074 |
rs774317503 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488642 | AATGTGGCCTCTTTC[-/C]TTTTTTTTTTTTTTT | 2074 |
rs774342646 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49501555 | TAAAGTTAAAAAAGG[A/G]AAAATACAAAAAAAT | 2074 |
rs774362169 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499469 | TGGAGAGTAGGAAGA[A/C]CTTTCGGCAGTTGCT | 2074 |
rs774381329 | snp | A/G | 3.30628e-05 | 0.00406575 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470899 | CAGTTCCTGTAAAGA[A/G]GAAAAACACCACTAA | 2074 |
rs774391199 | snp | C/T | 1.64988e-05 | 0.00287213 | missense | ERCC6 | GRCh38.p7 | 10:49474166 | TCATCAGGAAGACCT[C/T]TGAGATTCTTGGGAC | 2074 |
rs774425283 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | ERCC6 | GRCh38.p7 | 10:49473556 | TAGGTATACTTTTGG[A/G]CTCTAAGGAATACTT | 2074 |
rs774426918 | snp | C/G/T | 3.29545e-05 | 0.00405911 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516870 | GGAGAGTCATCTTTA[C/G/T]GTGCGTATGAGGGAT | 2074 |
rs774457970 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495680 | ATTTTGTCCCACTGT[C/T]CAGGTGCCCAAATCA | 2074 |
rs774463252 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | ERCC6 | GRCh38.p7 | 10:49532823 | CGTCACCCACAGAAC[A/G]AAAGGAGAGGTACTC | 2074 |
rs774508618 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473470 | CCCTGTTACATTCAC[A/G]TGTTACCTCATTGTA | 2074 |
rs774519700 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495621 | CGCCATCCTCCCCTA[-/C]CCTGGCTGTCCCCTG | 2074 |
rs774548546 | snp | A/G | 6.61026e-05 | 0.00574865 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472343 | CAAGACTCTGGGAAC[A/G]CACAGCCAAGAGTGG | 2074 |
rs774558508 | snp | C/G | 1.65252e-05 | 0.00287443 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472487 | TGCAACAGAGAGAGA[C/G]AGACCTCTCAACGAG | 2074 |
rs774616361 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515699 | GATTGATGCCCGATA[C/T]TTATCAATGTTTTCA | 2074 |
rs774621443 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508302 | TAAACTTTATTGATA[C/T]ATGATGACCATTTCC | 2074 |
rs774635843 | snp | C/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520310 | ATCAGTCTGTGGGTG[C/G]GGAAGCTTTGCTCTC | 2074 |
rs774636240 | snp | A/T | 1.85986e-05 | 0.00304942 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476336 | GAAAAACAAGGAAAC[A/T]ATAATTTCAAAAAAA | 2074 |
rs774638955 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463984 | AGTGGGGAGGTGCGC[G/T]CCTGAAAAGATATCC | 2074 |
rs774641572 | snp | C/T | 1.64795e-05 | 0.00287045 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516749 | TCTACCTGCTACGGG[C/T]TGTACAGTTAGGTCG | 2074 |
rs774657296 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463358 | GTGCACAAAAAGTTT[C/T]GGATTTTAGAGCATT | 2074 |
rs774675720 | in-del | -/CA/CACT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537509 | ATATATATACACATA[-/CA/CACT]CACACACACACACAC | 2074 |
rs774743557 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524490 | TGGCTTTCTTGTTTG[A/G]TTTGTTTTTATTTTG | 2074 |
rs774749613 | snp | A/C/T | 3.32128e-05 | 0.00407499 | intron-variant, synonymous-codon, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516347 | AACAAATTTCATGCA[A/C/T]CTCTCATTAAGTTTG | 2074 |
rs774791374 | in-del | -/G | 1.64802e-05 | 0.00287051 | ERCC6 | 10 | allele_origin=G(germline)/(germline) | 10:49482759 | ATAAACACAGGCAAC[-/G]GTGCCTAACTTTCCC | 2074 |
rs774814728 | snp | A/G | 4.9436e-05 | 0.00497148 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516746 | AACTCTACCTGCTAC[A/G]GGTTGTACAGTTAGG | 2074 |
rs774828577 | snp | A/C | 1.6788e-05 | 0.00289719 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474279 | GTACACTCAGATGAC[A/C]CCATGTAAAGTAAGA | 2074 |
rs774833290 | snp | A/C/T | 3.32575e-05 | 0.00407773 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524318 | GGGAAATACTCAGAC[A/C/T]CTTCACCCTCAGAGT | 2074 |
rs774865995 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496702 | AATCCCAGCTACTTG[A/G]GAGGCTGAGGCAGGA | 2074 |
rs774868539 | in-del | -/CTGTTTGA | 1.648e-05 | 0.0028705 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49515440 | TCGCGTTTGCTTTCC[-/CTGTTTGA]CTGTTTGACTATCAC | 2074 |
rs774900204 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49486271 | AAGAGGATGCAAAGG[A/G]TTTGAGTATCACCAT | 2074 |
rs774913453 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458813 | TTAGGAAGCAATGTT[A/G]TTTAGCAGTATTCTG | 2074 |
rs774918108 | snp | A/G | 2.59622e-05 | 0.00360284 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488221 | TTATTATGGAGGCTC[A/G]AGAGACCAATCCCTC | 2074 |
rs774929345 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49493309 | ATATACAGTCATCAA[A/C]TGCTCAAAAGATCCC | 2074 |
rs774930802 | snp | C/T | 3.32292e-05 | 0.00407597 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493264 | AAACCTGCATCCAAA[C/T]GTCCAAGAAGAAAAC | 2074 |
rs774975920 | snp | C/T | 9.88484e-05 | 0.00702954 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515641 | TTTGTAAGACCAGTT[C/T]GAAACAGAACAAAAG | 2074 |
rs774988483 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490012 | CATGAAAGTTGCTCT[A/G]TATTAGAAAAAAGGA | 2074 |
rs775001851 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49491163 | GCCTATGGAAAGGAA[A/C]TATTAATACATTTCC | 2074 |
rs775017022 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515782 | GCTGCTGAACTTGTA[C/T]CTTCTTTTTCAGTTT | 2074 |
rs775089627 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | ERCC6 | GRCh38.p7 | 10:49459123 | TTCTAGCTCTCATTT[C/T]AGCCAAGAGTGAGGA | 2074 |
rs775099060 | in-del | -/TATATATACACTTTCCTGATACACATATCTGAATTCTTG | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507923 | TAGAAACTGAACAGA[lengthTooLong]ATATATATACACTTT | 2074 |
rs775100105 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529821 | GCAATGTATTTTCAC[A/C]AAGGGGTACATAAAT | 2074 |
rs775119058 | snp | C/T | 3.29614e-05 | 0.00405951 | missense | ERCC6 | GRCh38.p7 | 10:49471001 | GCACTTGTTTCAGTG[C/T]TCTGGGATGCATCAG | 2074 |
rs775122052 | snp | C/T | 6.60142e-05 | 0.0057448 | missense | ERCC6 | GRCh38.p7 | 10:49474175 | AGACCTTTGAGATTC[C/T]TGGGACCTCCAGAAA | 2074 |
rs775140608 | snp | A/G | 1.65026e-05 | 0.00287246 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483538 | CCACAATAAAATGGT[A/G]AAGTCAGTTTTAAAT | 2074 |
rs775151137 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454956 | ATTTTTTAAAGGTGC[C/T]AGGGAAACTAGCTAT | 2074 |
rs775164694 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | ERCC6 | GRCh38.p7 | 10:49459051 | TGGGCAGCAGGGCAG[A/G]AGCTTCCTGCAGGTG | 2074 |
rs775231069 | snp | A/T | 6.69266e-05 | 0.00578436 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505848 | GTACATAATGGCTTG[A/T]TAGCAAATAGAAAGG | 2074 |
rs775262890 | snp | C/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540461 | AAGTAAAAGCAGATA[C/T]ATAGTGGATCCCAAC | 2074 |
rs775274710 | snp | G/T | 1.64844e-05 | 0.00287087 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530849 | ACATGACCTGAAAAA[G/T]AAGATAAATTGTCTA | 2074 |
rs775276232 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512143 | TTGAGCCAGCAGGAG[C/T]TCAGTTCAACCCCCA | 2074 |
rs775281005 | snp | A/G | 1.78426e-05 | 0.00298681 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517156 | TTATTAGTCCTAGTG[A/G]TAGTGGTTTTGCCTA | 2074 |
rs775291191 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49530744 | CTTCTGTCGTTTTAC[A/G]GAATCTAGTTTCCTG | 2074 |
rs775293209 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536076 | AGCTGAGATCACACC[A/G]CAGAACTCCAGCCTG | 2074 |
rs775300449 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49476601 | ACAGACCATCCTCCA[C/T]GTTAGCCTCCAAGTG | 2074 |
rs775330498 | snp | C/T | 1.75127e-05 | 0.00295906 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482658 | TTAAATATTAAAATG[C/T]CAAAAGTATTATCAT | 2074 |
rs775370737 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485637 | AAGGTACACAGGCAA[C/T]AGATATTTAATTCTT | 2074 |
rs775391300 | in-del | -/ATG | 6.59109e-05 | 0.0057403 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530673 | ATTAAGTGCCCCTAA[-/ATG]ATGACTTTTTCAAAA | 2074 |
rs775424153 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | ERCC6 | GRCh38.p7 | 10:49470231 | GTCATTGCTCTGTTC[C/G]TTGGCCTCACTCTTG | 2074 |
rs775442509 | snp | G/T | 3.00251e-05 | 0.00387448 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461587 | ATAGCAAAGTGATAT[G/T]TCACTCTGTATGCAA | 2074 |
rs775467281 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499351 | TAACTTAACGAAAGA[A/G]TAAGAAATAAAACAC | 2074 |
rs775488103 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456080 | CAAAATAAGGATGGT[A/G]TAAGGCCATTAATAT | 2074 |
rs775502652 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511252 | ACAAAAGAAGCACCT[C/T]CTTATGAAAGAATTC | 2074 |
rs775513617 | snp | A/C | 1.64925e-05 | 0.00287158 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515807 | CAGTTTCTGGGAGTA[A/C]CGACTGACAAGACAC | 2074 |
rs775531195 | snp | A/T | 1.65091e-05 | 0.00287303 | missense | ERCC6 | GRCh38.p7 | 10:49461392 | TCCCCCTGTGGCCAG[A/T]CCAGGTGGGAACACC | 2074 |
rs775532307 | snp | C/T | 4.94964e-05 | 0.00497451 | missense | ERCC6 | GRCh38.p7 | 10:49471083 | TTTGTTTTGGGTCTT[C/T]TAGCACTCTATTTGT | 2074 |
rs775539936 | snp | A/C | 0.00013214 | 0.00812726 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474012 | CTGTTTCCCGTCTGA[A/C]GTCTGTGCACTCACC | 2074 |
rs775540381 | snp | A/C | 1.64735e-05 | 0.00286993 | stop-gained | ERCC6 | GRCh38.p7 | 10:49532649 | GAAGCACTCCCTGTT[A/C]CAGCACGTCCTGGTC | 2074 |
rs775549101 | snp | C/G | 9.91146e-05 | 0.007039 | missense | ERCC6 | GRCh38.p7 | 10:49470865 | TTTAGATGGCATTTG[C/G]GTGTCTGAACATCTG | 2074 |
rs775556780 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498678 | AGCATTGATAGTTAA[C/T]TGATTACAGCTGCTG | 2074 |
rs775594609 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | ERCC6 | GRCh38.p7 | 10:49532739 | GGATCTGATGTCGGT[C/T]GATGTGCAGCAGGGC | 2074 |
rs775685925 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478311 | GAAGGGAAAGACACA[C/T]TTGTGCTTTAGGAAT | 2074 |
rs775707591 | snp | A/T | 1.64901e-05 | 0.00287137 | missense | ERCC6 | GRCh38.p7 | 10:49470435 | CTTATAAAAATTATT[A/T]TCCATTTGTTTATTC | 2074 |
rs775726140 | in-del | -/CA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538561 | CCTGCCTCATCCGCC[-/CA]CACTCTTATCAATTT | 2074 |
rs775775611 | snp | C/T | 1.66801e-05 | 0.00288787 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493285 | AGAAGAAAACAACCA[C/T]GAAAGAGCATATACA | 2074 |
rs775786952 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49530831 | TTGCCTTAGGGATGT[C/T]GTACATGACCTGAAA | 2074 |
rs775788034 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488502 | GCAGAACAAGCCCAG[C/T]ATCTATCATGTCTTC | 2074 |
rs775809191 | snp | C/G/T | 3.29534e-05 | 0.00405904 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515723 | GTTTTCATCAGCTCT[C/G/T]TCTACGCCTCCCATG | 2074 |
rs775850810 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524605 | TTTTGCTTGATCTGC[C/T]AAATACTTTTCGAAG | 2074 |
rs775870100 | snp | A/G | 1.67598e-05 | 0.00289476 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515371 | AACACTTCACATGTA[A/G]GGCAACATCACATTT | 2074 |
rs775870351 | snp | A/C | 1.64814e-05 | 0.00287061 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516635 | ATATAAGTTGGAGTA[A/C]TTGACAATGAGTTCA | 2074 |
rs775881690 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494197 | ACATTGTATGATCTC[A/G]GGCACACCATTTAAC | 2074 |
rs775886925 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513903 | GAAAGAAAGGAAGCT[A/G]TCCAAGATTACCAAT | 2074 |
rs775950707 | in-del | -/AAAT | 2.57828e-05 | 0.00359037 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476362 | AAAAAAAATTAACAG[-/AAAT]AATTAAAATATCAAC | 2074 |
rs775964421 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511257 | AGAAGCACCTTCTTA[C/T]GAAAGAATTCTTATG | 2074 |
rs775975145 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481599 | GGATGCACAGAAACC[A/G]TGCCTCCCACCCAGG | 2074 |
rs776004687 | snp | A/G | 3.35121e-05 | 0.00409328 | missense | ERCC6 | GRCh38.p7 | 10:49472919 | CAAACCTGCGTGTCC[A/G]TGCTTGGGTTCCAGT | 2074 |
rs776019768 | snp | A/G | 4.96323e-05 | 0.00498133 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472500 | GAGAGACCTCTCAAC[A/G]AGAATCCTTCCCAAT | 2074 |
rs776080529 | in-del | -/A | 0.0177088 | 0.0924165 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472887 | CTAATACATTCTTTT[-/A]AAAAAAAAAATAAAA | 2074 |
rs776082641 | snp | C/T | 5.40468e-05 | 0.00519812 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533008 | ATTTATAAGCCTTTT[C/T]GTTATATAGGATTCA | 2074 |
rs776098507 | snp | A/C | 3.29473e-05 | 0.00405864 | missense | ERCC6 | GRCh38.p7 | 10:49478432 | GTATGGATTTATGGT[A/C]TCTCGTAAGACACAT | 2074 |
rs776119091 | snp | C/G | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525607 | TAATAGGAAGGAATC[C/G]ATATTCTAAAATCTA | 2074 |
rs776149423 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524072 | TCATCTCCATCATCT[C/T]GGTATCTTCCCACTT | 2074 |
rs776161737 | snp | C/T | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515377 | TCACATGTAAGGCAA[C/T]ATCACATTTTTCACA | 2074 |
rs776162838 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533353 | GACACAAATGATTTA[C/T]AATATAGTGGCAAGA | 2074 |
rs776181099 | snp | A/C | 1.65968e-05 | 0.00288065 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461600 | ATTTCACTCTGTATG[A/C]AAGAAAGACACTTTT | 2074 |
rs776186015 | snp | A/G | 1.65916e-05 | 0.00288019 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476209 | AGCTTCTATTTTTTA[A/G]CTGACCTGCATCTCT | 2074 |
rs776222699 | snp | C/T | 0.000186341 | 0.00965069 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475358 | TTTTTAATGTGACTA[C/T]TAGAAAATTTACAAT | 2074 |
rs776252740 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490436 | CCAGGCTCACTGCAA[A/C]CTCCGCCTCTAGGGT | 2074 |
rs776319854 | snp | A/G | 4.99239e-05 | 0.00499594 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516180 | TTTTTACCCTGATAC[A/G]GCTGAAACCAGCAAA | 2074 |
rs776361424 | snp | A/G | 0.00016478 | 0.0090754 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482777 | GCCTAACTTTCCCGG[A/G]AAGATGAAGTCAAAG | 2074 |
rs776367874 | snp | A/C | 3.295e-05 | 0.00405881 | missense | ERCC6 | GRCh38.p7 | 10:49470716 | GATTAGAAGTTACTG[A/C]ATTTACTTCAGCTCC | 2074 |
rs776383043 | snp | A/T | 1.65291e-05 | 0.00287476 | stop-gained | ERCC6 | GRCh38.p7 | 10:49459222 | CTTTTCCCTCCTTTT[A/T]CATGATGCCATCCTA | 2074 |
rs776389883 | snp | C/T | 3.29489e-05 | 0.00405874 | missense | ERCC6 | GRCh38.p7 | 10:49470236 | TGCTCTGTTCCTTGG[C/T]CTCACTCTTGTTTTC | 2074 |
rs776406612 | snp | A/C | 0.000216398 | 0.0103996 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516120 | TCACTAAACTGAAGG[A/C]CAAGTGACGCACCGA | 2074 |
rs776462885 | snp | A/G | 1.64906e-05 | 0.00287142 | missense | ERCC6 | GRCh38.p7 | 10:49528500 | AGATGCTTTTGTTTT[A/G]CAGTGATCTTTTTTA | 2074 |
rs776488336 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477467 | CTTCCTCACCTCCAG[C/T]CACTCCTGAAGCCCG | 2074 |
rs776514960 | snp | C/T | | | missense | ERCC6 | GRCh38.p7 | 10:49500652 | ATTCCTCCTGCCTGC[C/T]GGCAGTGCAATTCCC | 2074 |
rs776522083 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511735 | CGACCCATCAGGGCA[C/T]TTTCTAACTCCTAAA | 2074 |
rs776536408 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518058 | AGCACAGCCTAAAAT[C/T]GCTAAATCCTCATCG | 2074 |
rs776545164 | snp | A/G | 1.64887e-05 | 0.00287125 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482855 | AATGATCCGATGAGG[A/G]GTGCGAAACTATTTG | 2074 |
rs776550240 | snp | A/G | 1.66233e-05 | 0.00288295 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528373 | GACTACAGGCATCAG[A/G]CATCAATTCAAGAAC | 2074 |
rs776574740 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490876 | GTGGGCACAGAAAGC[G/T]CATCCACTGTAAAAA | 2074 |
rs776607152 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473294 | ACATACACATGCCCA[A/C]AATCCCCGCCCCCAA | 2074 |
rs776621144 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473071 | ACACACACTTAAGAC[C/G]AGTTACAGTTCTCAG | 2074 |
rs776641969 | snp | A/G | 1.65427e-05 | 0.00287595 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506020 | TCCATCTCCTACCAT[A/G]AAAATAAAAATCACA | 2074 |
rs776656543 | snp | G/T | 4.94254e-05 | 0.00497094 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530716 | GAATGTTATTCTGAA[G/T]CACCTTATTATACTT | 2074 |
rs776663084 | snp | A/G | 0.000115438 | 0.00759643 | missense | ERCC6 | GRCh38.p7 | 10:49500592 | AGACCTGCCAAGAAG[A/G]CAATTATCTGGATGG | 2074 |
rs776675510 | snp | C/T | 3.30087e-05 | 0.00406242 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470967 | AATTAAATGATTTTA[C/T]GTAATACCTGCAAAA | 2074 |
rs776694423 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510076 | TGGTTTCCCTACATT[C/T]AGGTAGGAATGAGAA | 2074 |
rs776731401 | snp | A/G | 1.65269e-05 | 0.00287457 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49505943 | GTCAAATTCAGCATC[A/G]CTTTCCTCAGAATCG | 2074 |
rs776731520 | snp | A/G | 1.65946e-05 | 0.00288046 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516317 | TTCATCAAAGCTGAA[A/G]TATGTTTCATTTGGA | 2074 |
rs776752286 | snp | A/G | 3.30093e-05 | 0.00406246 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478514 | ACTATATATGTTTAA[A/G]GAACGCATTTGTTCT | 2074 |
rs776789596 | snp | A/C | 1.65045e-05 | 0.00287263 | missense | ERCC6 | GRCh38.p7 | 10:49461412 | GTGGGAACACCAGAC[A/C]CTGCTCCCAGACACC | 2074 |
rs776812752 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536811 | GAAATGGTAGCGCAA[A/C]AGAGTCACGGGGTTG | 2074 |
rs776814633 | snp | C/T | 1.64895e-05 | 0.00287132 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530858 | GAAAAATAAGATAAA[C/T]TGTCTATTTTGCACT | 2074 |
rs776817300 | snp | G/T | 1.65537e-05 | 0.0028769 | missense | ERCC6 | GRCh38.p7 | 10:49472947 | AGTCTGGGTCATAGA[G/T]GACAACTCTGTTTGC | 2074 |
rs776827846 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49472773 | GGGTGTCTTCTTTCA[A/C]GTTGAAGAACAGGAG | 2074 |
rs776842694 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484878 | ACACTAAAAATGTCC[A/G]AAGGCAAAGAGGAAA | 2074 |
rs776852962 | in-del | -/ACTC | 1.6641e-05 | 0.00288448 | frameshift-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524310 | CCTCTGTGGGGAAAT[-/ACTC]AGACTCTTCACCCTC | 2074 |
rs776871580 | snp | C/T | 3.2969e-05 | 0.00405998 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515932 | CAAATGTGCCTCTTT[C/T]TTTTTTCTTTAAAGC | 2074 |
rs776908392 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528256 | AGGGATTTGGTTCTG[C/T]AGGTGTAGAGAATAA | 2074 |
rs776925428 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515582 | ACGAAACTCCAGAAA[A/G]TCCACTGGTTTCTCA | 2074 |
rs776926130 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499311 | TCTAAAACTCCAAAC[A/G]CTCCTCACAGAAGTA | 2074 |
rs776932449 | snp | C/G | 1.675e-05 | 0.00289391 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493293 | ACAACCATGAAAGAG[C/G]ATATACAGTCATCAA | 2074 |
rs776989320 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49532825 | TCACCCACAGAACGA[A/C]AGGAGAGGTACTCCT | 2074 |
rs777002239 | snp | C/G | | | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524172 | CATCATCAATCTCCT[C/G]CACTGGCACTTTCTT | 2074 |
rs777009906 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532746 | ATGTCGGTCGATGTG[C/T]AGCAGGGCTGGCCCT | 2074 |
rs777015742 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49498382 | ATTTGACCTTAAGAG[C/T]TATTTTTCTGTAAGA | 2074 |
rs777045356 | snp | A/G | 1.65217e-05 | 0.00287412 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483559 | AGTTTTAAATAAGAA[A/G]TGACACCCTTTCAAT | 2074 |
rs777051514 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463053 | ATAAACTGTGGTACA[A/G]GTTGAATATCTCTTA | 2074 |
rs777122101 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | ERCC6 | GRCh38.p7 | 10:49470655 | AGCCTATCATTGCTA[A/G]TTACATTACTACTCA | 2074 |
rs777136413 | snp | A/G | 1.6477e-05 | 0.00287024 | missense | ERCC6 | GRCh38.p7 | 10:49470547 | CCAGATGGCATAGAA[A/G]TTTTGCCTGTTCCTG | 2074 |
rs777194124 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49508364 | TAAATTTCCCACCAC[A/T]TCACTCTGCATCGAC | 2074 |
rs777224849 | snp | A/C/G | 6.59232e-05 | 0.0057409 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516638 | TAAGTTGGAGTACTT[A/C/G]ACAATGAGTTCAATG | 2074 |
rs777226382 | snp | C/T | 1.65209e-05 | 0.00287405 | missense | ERCC6 | GRCh38.p7 | 10:49473013 | TGGTCAGAAGAAACA[C/T]AAATATGGATGTGTC | 2074 |
rs777251839 | snp | A/T | 0.000163972 | 0.00905312 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472898 | CTTTTAAAAAAAAAA[A/T]AAAAACAAACCTGCG | 2074 |
rs777252763 | snp | A/T | 1.64947e-05 | 0.00287177 | missense | ERCC6 | GRCh38.p7 | 10:49500539 | AGAGGAGCACTTGCC[A/T]GTAATTTGAACCACG | 2074 |
rs777302913 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524564 | GCTCTTTTATTACAA[C/T]CTTGCTTCTTCCTTT | 2074 |
rs777366470 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464585 | GGCAACCCCTCCCAT[C/T]ACAGGCCCAGAGGCC | 2074 |
rs777367194 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | ERCC6 | GRCh38.p7 | 10:49459077 | AGGTGCCCGCTTTCA[C/T]TTTCTAAACGCTCTG | 2074 |
rs777387031 | snp | A/C | 1.64735e-05 | 0.00286993 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532806 | AGCAGAGGTGGACAG[A/C]CCGTCACCCACAGAA | 2074 |
rs777390307 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484033 | ACTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 2074 |
rs777400318 | snp | A/G | 1.64846e-05 | 0.0028709 | missense | ERCC6 | GRCh38.p7 | 10:49474145 | AACTGATCTTCTTCT[A/G]GTTCATCATCAGGAA | 2074 |
rs777446958 | in-del | -/T | 1.65136e-05 | 0.00287342 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49505967 | GAATCGTCCTCCAGC[-/T]TTCAGACGTTTCTCT | 2074 |
rs777473180 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526851 | AGGAACTCAAAAAAA[A/G]AGCAAAGCCAGATGT | 2074 |
rs777474123 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489035 | TGATCCGCCGGCCTC[A/C]GCCTCCCAAAGTGCT | 2074 |
rs777478670 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | ERCC6 | GRCh38.p7 | 10:49530803 | GGCTAAGCTGTTCAA[C/T]AATTTTATTGATTTG | 2074 |
rs777487555 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538457 | AGATGATGGGAAAAG[C/T]TGAGGAGAAAAGCGA | 2074 |
rs777489340 | snp | C/T | 8.23893e-05 | 0.00641778 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515535 | TCTGGAGGATGACCA[C/T]GGGTCTCCAGATAAT | 2074 |
rs777511263 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492238 | CGTGCATCTGACTCC[A/G]TGAGGCAAACACTCC | 2074 |
rs777512127 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509157 | TCCTCCACTGAGATG[C/G]GGAGAACAGCAGCAC | 2074 |
rs777559398 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538942 | TGCCCGACATTCGGC[C/T]GGGACCCCCGAACAC | 2074 |
rs777568431 | snp | C/T | 1.64993e-05 | 0.00287218 | missense | ERCC6 | GRCh38.p7 | 10:49470496 | GGTCTTTCTCTTTTG[C/T]AAGAAAGACCTAACT | 2074 |
rs777595530 | snp | G/T | | | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516349 | CAAATTTCATGCATC[G/T]CTCATTAAGTTTGCT | 2074 |
rs777618785 | snp | A/G | 1.66538e-05 | 0.00288559 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461343 | GTATGGCATGCAGCA[A/G]TCTCTTACTTTTTTC | 2074 |
rs777652521 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | ERCC6 | GRCh38.p7 | 10:49470290 | TTTTCTTCACCAGGT[A/G]TGGAATTCGAGTTCC | 2074 |
rs777672154 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534071 | CCCAGGAGGCGGAGG[C/T]TGCAGTGAGATGAGA | 2074 |
rs777672678 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524626 | CTTTTCGAAGCCTGA[C/T]GCTTCATTAAGCATG | 2074 |
rs777682190 | snp | A/G | 2.33032e-05 | 0.00341337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488187 | TTGTCATTAGAAGAT[A/G]TCTGTGAAAGGGCTG | 2074 |
rs777687695 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460238 | GTGCATCGTAAATCA[G/T]AGCGTGCAACACAAA | 2074 |
rs777700067 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517375 | AAACTCACATCACTT[G/T]TTGACAAGCTCCCAG | 2074 |
rs777727975 | snp | C/T | 1.65149e-05 | 0.00287353 | missense | ERCC6 | GRCh38.p7 | 10:49472992 | CACCTAAGCCGCCCA[C/T]CCGCGTGGTCAGAAG | 2074 |
rs777770092 | snp | A/T | 1.64773e-05 | 0.00287026 | missense | ERCC6 | GRCh38.p7 | 10:49483471 | TGTAGGAGTAAGATG[A/T]GATCAAAATTCCATG | 2074 |
rs777780746 | snp | A/G | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540116 | CGATGTGGGCTCACT[A/G]CAACCTCCTCCTCCC | 2074 |
rs777790671 | snp | C/G/T | 6.59179e-05 | 0.00574068 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515447 | TTGCTTTCCCTGTTT[C/G/T]ACTATCACATGATTT | 2074 |
rs777797420 | snp | A/G | 1.64792e-05 | 0.00287042 | missense | ERCC6 | GRCh38.p7 | 10:49482823 | CGGAGGTTATTTTGC[A/G]TCGGTGAGCCAGACA | 2074 |
rs777806154 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478349 | TAACTCCTGGATTTA[C/T]AGACCTGTTCATTTT | 2074 |
rs777886483 | snp | C/T | 4.9534e-05 | 0.0049764 | missense | ERCC6 | GRCh38.p7 | 10:49505983 | TTCAGACGTTTCTCT[C/T]TGTCCTGCAGTCTCA | 2074 |
rs777889402 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467418 | TTTAGCCATTCTAGA[C/G]GGTGTATAGTGGTAT | 2074 |
rs777894815 | in-del | -/A | 3.29538e-05 | 0.00405904 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49516665 | AATGACCTCGTCATC[-/A]AGAAAAAGTTCAAGA | 2074 |
rs777906196 | snp | C/T | 4.96309e-05 | 0.00498131 | missense | ERCC6 | GRCh38.p7 | 10:49505915 | ACAGAAAACCTGGCA[C/T]TTTAAAACCTTCGTC | 2074 |
rs777931939 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470213 | CTTTTCCAAAACATA[A/G]TCGTCATTGCTCTGT | 2074 |
rs777933493 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465856 | ATTGCCCAGTCTCTG[G/T]TATGTCTTTATCAGC | 2074 |
rs777979018 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479687 | GCCCCCACATCCTCC[C/T]TCCACCCACACCCCC | 2074 |
rs778021254 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497554 | AATTTCTGCCATTTT[-/C]CCCCTTAGTAGAAAA | 2074 |
rs778042204 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518714 | CCTCAGAACAGTGGA[C/T]GTGCACAACCCAACC | 2074 |
rs778075023 | snp | C/G | 1.65471e-05 | 0.00287633 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524259 | ACAGGTCCGCCTCTG[C/G]CCCCTCCACCTCGTC | 2074 |
rs778084447 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474533 | TCACTAGAAAAAAGG[A/T]ATGCAGTTCACGGTA | 2074 |
rs778141050 | snp | C/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523519 | TGGCTTATAATTATG[C/G]AGATGACTATTTTCT | 2074 |
rs778176359 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487863 | ATTAAAAAGATGCTT[A/G]TGTAAAAAGAACAAG | 2074 |
rs778177594 | snp | A/G | 3.30934e-05 | 0.00406763 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49493242 | TTACAGTTGGACCCA[A/G]CCCCTCAAACCTGCA | 2074 |
rs778182071 | snp | C/G | 1.65288e-05 | 0.00287474 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472333 | ATTCCCTGCTCAAGA[C/G]TCTGGGAACGCACAG | 2074 |
rs778197774 | snp | A/T | 3.30077e-05 | 0.00406236 | missense | ERCC6 | GRCh38.p7 | 10:49470841 | CCAAAGGCTGGTTGA[A/T]TCCTTCTTTTTAGAT | 2074 |
rs778202159 | snp | C/T | 4.96619e-05 | 0.00498282 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473992 | GGCTGTCATAAAGAA[C/T]CAGCCTGTTTCCCGT | 2074 |
rs778203172 | snp | A/T | 3.33317e-05 | 0.00408224 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482897 | CACCTTTTTATTAAA[A/T]TTACCTTTTAGCAAT | 2074 |
rs778203287 | snp | A/G | 3.31779e-05 | 0.00407282 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458778 | TCAGAAATGCCCGTT[A/G]GAAAAAGGGACTTGA | 2074 |
rs778254786 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481361 | AAAAGAATGGTATAA[C/G]AGGAGATTCAGAGAA | 2074 |
rs778258203 | snp | A/G | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540955 | CCTAGCAAGCATACT[A/G]TTCACCTCTTCCCAG | 2074 |
rs778263770 | snp | A/C | 1.6486e-05 | 0.00287102 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515854 | CACCAGATGAGGCAA[A/C]AGTGACAACACTGTT | 2074 |
rs778301764 | snp | C/T | 4.95536e-05 | 0.00497738 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472996 | TAAGCCGCCCACCCG[C/T]GTGGTCAGAAGAAAC | 2074 |
rs778309552 | in-del | -/TGTAA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526597 | TAACAAATCTTTTCC[-/TGTAA]TTTACACTGAGTATT | 2074 |
rs778353486 | snp | C/T | 1.65012e-05 | 0.00287234 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49517049 | TATCACTATAGCACT[C/T]GCTTCTATGCTGTCA | 2074 |
rs778353556 | snp | A/G | 3.29707e-05 | 0.00406008 | intron-variant, stop-gained | ERCC6, PGBD3 | GRCh38.p7 | 10:49515770 | TGATCATGTTTGGCT[A/G]CTGAACTTGTATCTT | 2074 |
rs778356719 | snp | A/C | 1.64787e-05 | 0.00287038 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515459 | TTTGACTATCACATG[A/C]TTTATGCCATCATAA | 2074 |
rs778370093 | snp | A/C | 1.64749e-05 | 0.00287005 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516934 | GAATAAGATACGCAG[A/C]TGTGTGCAACAAAGA | 2074 |
rs778371741 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499276 | ACATCTATATAAATG[A/C]AACTGGCGTTCTAAA | 2074 |
rs778377365 | snp | A/G | 3.29886e-05 | 0.00406118 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478504 | AGGGAACATTACTAT[A/G]TATGTTTAAGGAACG | 2074 |
rs778388707 | snp | A/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455680 | TTTGTTTAGGGGAGC[A/T]ATCCTAAAAGATAAA | 2074 |
rs778394934 | snp | A/C/T | 3.29849e-05 | 0.00406098 | missense | ERCC6 | GRCh38.p7 | 10:49470505 | CTTTTGTAAGAAAGA[A/C/T]CTAACTTTTCATCAA | 2074 |
rs778402458 | in-del | -/GAGATACAAACAGCC | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457842 | CACATAAACAGTAGT[-/GAGATACAAACAGCC]TTGGCTGGAATCCAA | 2074 |
rs778457703 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49512997 | TTCATTATACACCCT[A/C]CTTCACGGTTCTCAC | 2074 |
rs778457795 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516853 | TAGATGGAACTTCAT[C/T]AGGAGAGTCATCTTT | 2074 |
rs778461443 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515562 | TAATGGCATACCACA[C/T]GTCGACGAAACTCCA | 2074 |
rs778477262 | snp | C/T | 8.4533e-05 | 0.00650072 | missense | ERCC6 | GRCh38.p7 | 10:49461503 | CCACCAGTACATAAT[C/T]TGGGCTGGCTCCATC | 2074 |
rs778495061 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475909 | ATGTACCTGACACCC[A/G]CCCACCTACCAGGTA | 2074 |
rs778562892 | snp | C/T | 0.000131776 | 0.00811608 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524573 | TTACAACCTTGCTTC[C/T]TCCTTTCAAAAGACA | 2074 |
rs778585863 | snp | C/T | 1.65067e-05 | 0.00287282 | missense | ERCC6 | GRCh38.p7 | 10:49493136 | TTGTGGGTATAGGAA[C/T]CGGTTTCATGTAGAA | 2074 |
rs778604589 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49536702 | GATCTCCCCAGCCCT[C/G]CAAAGCCATAGACTG | 2074 |
rs778610099 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524148 | CTTCCCCAGAACTTG[A/G]GAAAAAGTCATCATC | 2074 |
rs778615795 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513972 | CCAGAGTCTATATTC[C/T]TATCTGTTACATAAT | 2074 |
rs778624078 | snp | A/G | | | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459019 | CATCTCCACCAGAAG[A/G]TCATCGTGTTCTGTG | 2074 |
rs778638047 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507632 | TGCAATGGTGTACAA[C/T]AATCGTTCTTGACAG | 2074 |
rs778671522 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515660 | ACAGAACAAAAGAGG[A/G]CTTGAATACCATTTC | 2074 |
rs778696406 | in-del | -/AT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475304 | GATATATGAAATAAA[-/AT]ATATATCAAAATTAA | 2074 |
rs778727549 | snp | A/G | | | | | GRCh38.p7 | 10:49506336 | TAAGACATGAAATTA[A/G]TCCTAGAAAAGATTC | 2074 |
rs778765560 | in-del | -/C | 1.65049e-05 | 0.00287266 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474021 | TCTGAAGTCTGTGCA[-/C]CTCACCTGCCTTGAC | 2074 |
rs778782073 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459736 | TAAAAAAACACAAAT[C/G]TAACTCTGAAAGGGT | 2074 |
rs778799607 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488578 | CTTTGCATTCTATTA[C/T]AATTTGTGTACTCAG | 2074 |
rs778844406 | snp | A/T | 1.68176e-05 | 0.00289974 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476187 | TTGGTCCACAATTCA[A/T]TTCTCCAGCTTCTAT | 2074 |
rs778864478 | snp | A/C | 1.67363e-05 | 0.00289272 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474268 | AAAGAGTACATGTAC[A/C]CTCAGATGACCCCAT | 2074 |
rs778868208 | snp | G/T | 2.44245e-05 | 0.00349452 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488202 | GTCTGTGAAAGGGCT[G/T]CTGTTATTATGGAGG | 2074 |
rs778871384 | snp | A/G | 3.29511e-05 | 0.00405887 | missense | ERCC6 | GRCh38.p7 | 10:49459087 | TTTCACTTTCTAAAC[A/G]CTCTGGCAGAATCAG | 2074 |
rs778873369 | snp | A/G | 0.00013182 | 0.00811742 | missense | ERCC6 | GRCh38.p7 | 10:49470641 | TTGTCTCTTCTCCAA[A/G]CCTATCATTGCTAGT | 2074 |
rs778883160 | in-del | -/CA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49479316 | AAAAAAGAGCTTGAC[-/CA]CACACACAGAAAAAA | 2074 |
rs778886819 | snp | C/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457188 | AAAAAGGAAGGAGTT[C/T]TGACTTTCTTCTAAG | 2074 |
rs778904435 | snp | C/T | 1.78697e-05 | 0.00298907 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528573 | CAATGAAGTGATTTA[C/T]TGTTAAATACAAAAG | 2074 |
rs778904927 | in-del | -/A | 1.6528e-05 | 0.00287467 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49500681 | CCACAGCCACCTAAC[-/A]CCTGTCTGCTGGTAC | 2074 |
rs778957150 | snp | C/T | 1.65375e-05 | 0.0028755 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474003 | AGAACCAGCCTGTTT[C/T]CCGTCTGAAGTCTGT | 2074 |
rs778974002 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465638 | AGGTGACTGAATTAT[A/G]GGGTTGGGTCTTTCC | 2074 |
rs778979020 | snp | C/G | 0.000115828 | 0.00760924 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532509 | TGTCATGTTTTACCA[C/G]CACTTTGAAAGGAAG | 2074 |
rs779031151 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502905 | TCATGAACTGGCTAC[A/T]CTAGAATAATCTCAA | 2074 |
rs779085147 | snp | C/G | 1.64749e-05 | 0.00287005 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516952 | TGTGCAACAAAGAAC[C/G]TGGCAGATTATTTAT | 2074 |
rs779086787 | snp | C/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521857 | ATGGAAAGGGCTTGA[C/G]GGAAAATTCCTAGTA | 2074 |
rs779092544 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462497 | GACTGACAATTTTTT[-/A]TAAAAAAAAACCTGT | 2074 |
rs779102527 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534496 | TGTTAAGTGAAAAAA[A/T]TCATGGTATGAACAC | 2074 |
rs779102963 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529165 | CACTGGGGAGGCCCA[A/G]TGAACTGGGCTTGTG | 2074 |
rs779112067 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465016 | CCACGGTCCTCCAGA[C/T]CCCAGAACAGTAGAT | 2074 |
rs779112281 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49478190 | GTCAAAGCCTGTGGA[C/T]TAGAGAAGAATCCAC | 2074 |
rs779141499 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459936 | TTTTAACCACAGTAG[C/T]ACTCAAGGCAAGCAG | 2074 |
rs779153104 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | ERCC6 | GRCh38.p7 | 10:49470377 | GATGTTTCTCCAGGG[C/T]CTCTTCTTCTGCCAC | 2074 |
rs779154837 | snp | A/T | 1.6486e-05 | 0.00287102 | missense | ERCC6 | GRCh38.p7 | 10:49458831 | TAGCAGTATTCTGGC[A/T]TGAGTTTCCAAATTC | 2074 |
rs779180885 | in-del | -/CTC | 3.29568e-05 | 0.00405923 | cds-indel, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524109 | CTCCTCCTCCTCCTT[-/CTC]CTACAGAAGCAGCTT | 2074 |
rs779215216 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485593 | GAAAATAAAAGTGAA[C/T]TAAAAATTCCACCCT | 2074 |
rs779225876 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49511613 | TATTTTTTGGTGTAG[A/G]TGGGGTTTTGCCATA | 2074 |
rs779263208 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533729 | GATCACTTGAGCCTG[A/G]GAGATGGAGGCTGCA | 2074 |
rs779273831 | snp | A/G | 1.65299e-05 | 0.00287483 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461438 | ACACCGCTGACGAGA[A/G]AGCCTCAGTGCTTTC | 2074 |
rs779279311 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | ERCC6 | GRCh38.p7 | 10:49532720 | GCGCTAGGCTCTACT[G/T]CCTGGATCTGATGTC | 2074 |
rs779302809 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49478417 | CATTCTCCGCAGTAG[A/G]TATGGATTTATGGTA | 2074 |
rs779307613 | snp | C/T | 1.65817e-05 | 0.00287933 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517084 | TCTCTAAAAGGTCAG[C/T]TATTTCATGTAAACT | 2074 |
rs779327891 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497839 | CTCCATGGTCAAATA[C/T]ATCAACCTGCAGGAT | 2074 |
rs779357960 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49499180 | TTTGAAAAAATCCCC[-/T]GCTTCAATATAACTT | 2074 |
rs779361736 | snp | C/T | 1.65252e-05 | 0.00287443 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470940 | TATCATCTTGTGCAA[C/T]TGATTACTTTAAATT | 2074 |
rs779434811 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474361 | CTCCACCAGCTTCTT[A/G]GTTTCTTCTCTAGTC | 2074 |
rs779437937 | snp | C/T | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516801 | ATTTTTGTCATTTTC[C/T]TCCTCCTTGATGGTG | 2074 |
rs779471677 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526787 | TCCAATTTCAGTTCA[C/T]GTCTTCAAGTGTTGG | 2074 |
rs779500108 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510765 | AAAAGGAAGACACAG[A/G]CAGAGAAGCGTGACT | 2074 |
rs779520036 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465982 | TGACACTACTCTGGT[A/G]TTCCTTTTTGCATAT | 2074 |
rs779552713 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520259 | ACTTCCTAAGTCAGC[A/G]TCTCCAGTGTTAGGG | 2074 |
rs779596665 | snp | C/T | 1.76356e-05 | 0.00296943 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524793 | CTGAAAGAACAATAG[C/T]AATGCGTTTCGCACT | 2074 |
rs779596933 | snp | A/C | 1.64784e-05 | 0.00287035 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515675 | GCTTGAATACCATTT[A/C]TTTCCACGGATTGAT | 2074 |
rs779608430 | snp | A/T | 4.94287e-05 | 0.00497111 | missense | ERCC6 | GRCh38.p7 | 10:49470732 | ATTTACTTCAGCTCC[A/T]TTAGCCTCAGATTTC | 2074 |
rs779620359 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461611 | TATGCAAGAAAGACA[C/T]TTTTCTCCTCTGTAT | 2074 |
rs779669250 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497394 | GCATAAACACATGCA[C/T]ATGTTTTTTCAGGTT | 2074 |
rs779687046 | snp | C/T | 1.65149e-05 | 0.00287353 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49505994 | CTCTTTGTCCTGCAG[C/T]CTCAGTTTATTCCAT | 2074 |
rs779697013 | snp | A/C | 1.64866e-05 | 0.00287106 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472423 | AGTCAGGAGCCTGTA[A/C]ACAGTCACTTGCTTC | 2074 |
rs779758553 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469738 | AATTGTTGAGTCTAC[-/A]TCTCCTAACTTTTCT | 2074 |
rs779761725 | snp | A/G | 1.65179e-05 | 0.00287379 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532531 | GAAAGGAAGAAGATG[A/G]GCTGCACTCACGTGA | 2074 |
rs779763531 | snp | C/T | 6.65236e-05 | 0.00576692 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505872 | AGAAAGGAAAGAACA[C/T]ATGGTACATACTTAA | 2074 |
rs779766147 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49530334 | CCCATTATAAACTGA[A/G]GAGCCTCTGGACTTA | 2074 |
rs779776917 | snp | C/G | 1.65811e-05 | 0.00287929 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516296 | ACCAAAATAAGGAAC[C/G]ATGAATTCATCAAAG | 2074 |
rs779799406 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480124 | GCCCTGCCCCAGCTG[A/G]GCACACCAACCCCAG | 2074 |
rs779845499 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518570 | ACTCCCGCCCCTGCC[C/T]CCACCTCCACTTGAT | 2074 |
rs779850702 | in-del | -/TGGTACCATCCATCTT | 1.64735e-05 | 0.00286993 | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49473520 | TTGAAGCTATTGTAG[-/TGGTACCATCCATCTT]TGGTACCATCCATCT | 2074 |
rs779874677 | snp | C/T | 1.66037e-05 | 0.00288125 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516393 | AATTTGGAAAATTTG[C/T]CCACTGGATCCAAAT | 2074 |
rs779902195 | in-del | -/A | 3.3065e-05 | 0.00406588 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470901 | GTTCCTGTAAAGAGG[-/A]AAAACACCACTAATA | 2074 |
rs779916118 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49493231 | TGGACAGACAATTAC[A/G]GTTGGACCCAACCCC | 2074 |
rs779937763 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513282 | TATACTGCCTCCTTA[A/G]GGAAAGTCAGCTAGC | 2074 |
rs779968358 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481182 | GAGGTGTGGGAGAGG[A/G]AGGGGAGGAATGGTA | 2074 |
rs779973315 | snp | C/T | 3.30983e-05 | 0.00406793 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516022 | GATGTCCCATTGAAC[C/T]GAGCTTATCAAGAAG | 2074 |
rs779986881 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49494666 | TCAGTGCATGGTACT[C/T]CCCTGAAACTCTCAC | 2074 |
rs779988885 | snp | A/G | 1.66558e-05 | 0.00288577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476201 | ATTTCTCCAGCTTCT[A/G]TTTTTTAGCTGACCT | 2074 |
rs780088061 | snp | A/G | 3.33684e-05 | 0.00408449 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460351 | GTCTCACCCTGGAAA[A/G]CAAAAAGGTTATCTA | 2074 |
rs780091693 | snp | C/G | 1.65228e-05 | 0.00287422 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470947 | TTGTGCAATTGATTA[C/G]TTTAAATTAAATGAT | 2074 |
rs780115098 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531670 | AACCATGAACGAGCA[C/T]CTGCTCCTGAGGAGG | 2074 |
rs780173506 | snp | C/T | 0.00013187 | 0.00811895 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49524013 | ACAGTACAATGTATT[C/T]ATAATCCCCACAGAC | 2074 |
rs780200260 | snp | A/G | 1.64789e-05 | 0.0028704 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474096 | CAACAAAGACTCAAC[A/G]ACAATCATTTTCCCA | 2074 |
rs780209326 | snp | A/G | | | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49453998 | CCTAGATGTTTTTCA[A/G]TCAATTTGGAGAGTT | 2074 |
rs780209673 | snp | A/G | 4.9423e-05 | 0.00497082 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470216 | TTCCAAAACATAATC[A/G]TCATTGCTCTGTTCC | 2074 |
rs780219667 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457477 | CCTCTCATGCAGTCC[A/G]GCAAGGCCCCCCTGC | 2074 |
rs780243148 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49502847 | AGCCCTAAGTGTCAA[C/T]TGTGTCAAGGTCGAG | 2074 |
rs780247230 | snp | A/T | 1.64817e-05 | 0.00287064 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515888 | ATTCCATCTGCAGAC[A/T]ATATTGCCTTTGCCA | 2074 |
rs780286121 | snp | A/C | 1.64754e-05 | 0.00287009 | missense | ERCC6 | GRCh38.p7 | 10:49483449 | ATGTCATCCTGCATC[A/C]ATCGAATGTAGGAGT | 2074 |
rs780287010 | snp | A/G | 1.64765e-05 | 0.00287019 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530695 | CTTTTTCAAAAATGC[A/G]ATACTGAATGTTATT | 2074 |
rs780287602 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49464930 | GGGCAGTGCAGAAGG[A/T]AAATGTTGGGTTGGA | 2074 |
rs780309557 | in-del | -/TTTATATATATATATATATATATATATA | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526115 | ATATATTTATATATT[-/TTTATATATATATATATATATATATATA]TTTATATATATATAT | 2074 |
rs780313873 | snp | A/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519510 | ACCATGCAGAGGAAC[A/C]AACTCAAATCCACTT | 2074 |
rs780332684 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49496579 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACCTGAA | 2074 |
rs780382121 | snp | A/G | 3.30595e-05 | 0.00406554 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49500681 | CCACAGCCACCTAAC[A/G]CCTGTCTGCTGGTAC | 2074 |
rs780423620 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471706 | TCACAGGATCCAACT[C/T]GTCCTCCACCCTCAC | 2074 |
rs780434796 | snp | C/T | 6.58924e-05 | 0.0057395 | missense | ERCC6 | GRCh38.p7 | 10:49532822 | CCGTCACCCACAGAA[C/T]GAAAGGAGAGGTACT | 2074 |
rs780446851 | snp | C/T | 1.64868e-05 | 0.00287109 | missense | ERCC6 | GRCh38.p7 | 10:49500571 | GTCCTGATCTTGCTG[C/T]AGCTCAGACCTGCCA | 2074 |
rs780448249 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510640 | TGGAAGCCACCTGGG[G/T]ACAAACACTGTCTTA | 2074 |
rs780469192 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49458990 | GTGTGGGCCTGGAAA[A/G]CGATGAAGTTTCTCA | 2074 |
rs780502665 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49510940 | AAAATGGTTAAGGTT[C/G]GCTACAAAAAAATGA | 2074 |
rs780509183 | snp | A/C | 1.65351e-05 | 0.00287528 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524684 | TGAGGGATCTGGGTA[A/C]CAAAAGGTGTCATCT | 2074 |
rs780527672 | snp | C/T | 1.66222e-05 | 0.00288285 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505874 | AAAGGAAAGAACATA[C/T]GGTACATACTTAAAA | 2074 |
rs780528575 | snp | A/C | | | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49538973 | TCACCCAGGGCCGCG[A/C]GAGCGCCCACAAGGA | 2074 |
rs780536109 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509351 | ATGTTCACTGAAAGA[A/C]GAGAAAGCAAGTTAC | 2074 |
rs780538788 | snp | A/C/T | 6.5995e-05 | 0.00574402 | missense, stop-gained | ERCC6 | GRCh38.p7 | 10:49482713 | AAGCATTTGAATATC[A/C/T]CCCCATGGTGATGGG | 2074 |
rs780557032 | snp | A/G | 1.65173e-05 | 0.00287374 | missense | ERCC6 | GRCh38.p7 | 10:49473000 | CCGCCCACCCGCGTG[A/G]TCAGAAGAAACACAA | 2074 |
rs780562398 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49463852 | ACATGACTGTGAGGC[C/G]TCCACAGCCACACAG | 2074 |
rs780575154 | snp | G/T | 1.65518e-05 | 0.00287674 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461447 | ACGAGAGAGCCTCAG[G/T]GCTTTCAGGGCATCC | 2074 |
rs780575521 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478509 | ACATTACTATATATG[C/T]TTAAGGAACGCATTT | 2074 |
rs780606871 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517557 | AACACTAGGCATAAA[C/T]AGGTTTTAAAAGTGT | 2074 |
rs780608655 | snp | C/G | 4.98418e-05 | 0.00499183 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524277 | CCTCCACCTCGTCAT[C/G]TTCCTCCTCTTCCTC | 2074 |
rs780612516 | snp | C/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540120 | GTGGGCTCACTGCAA[C/T]CTCCTCCTCCCAGGT | 2074 |
rs780637339 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485427 | ATACCATTTAAAATA[A/G]ATCATTAAAGCATAA | 2074 |
rs780652533 | snp | A/G | 3.35014e-05 | 0.00409262 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476313 | GGCAAAATAAGACCT[A/G]CGGACGGGAAAAACA | 2074 |
rs780661242 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477013 | CGGTGCTGCTGGAGA[A/G]AAGCTCATACATGGC | 2074 |
rs780684850 | snp | A/C | 3.36236e-05 | 0.00410008 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461325 | TGTTTGGACTCCTTG[A/C]AAGTATGGCATGCAG | 2074 |
rs780694810 | snp | C/T | 3.2956e-05 | 0.00405918 | missense | ERCC6 | GRCh38.p7 | 10:49532603 | AGCTGGGAGGCACGG[C/T]TGGCCTCATGGATGG | 2074 |
rs780697990 | snp | C/T | 1.64743e-05 | 0.00287 | missense | ERCC6 | GRCh38.p7 | 10:49532895 | TTTCTTCATTATTAC[C/T]GACAGGTTGACTCTG | 2074 |
rs780731619 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516923 | AGAGCCATCTTGAAT[A/G]AGATACGCAGCTGTG | 2074 |
rs780742421 | snp | A/G | 1.65285e-05 | 0.00287471 | missense | ERCC6 | GRCh38.p7 | 10:49493236 | AGACAATTACAGTTG[A/G]ACCCAACCCCTCAAA | 2074 |
rs780751990 | in-del | -/AA | 1.7569e-05 | 0.00296381 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49515338 | TGACACCTGCTATTC[-/AA]AGTGTGATATTCAAC | 2074 |
rs780795428 | snp | A/G | 4.94189e-05 | 0.00497062 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532671 | GTCCTGGTCATAGAC[A/G]TCCACACCCAAACCC | 2074 |
rs780831345 | snp | C/T | 3.29902e-05 | 0.00406128 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483313 | AATTATTCTTCTCCA[C/T]TTGGAAATCTCCCTT | 2074 |
rs780843888 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | ERCC6 | GRCh38.p7 | 10:49470392 | TCTCTTCTTCTGCCA[C/T]ACTATGATGTTTTGT | 2074 |
rs780874055 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49481421 | AAATCATTCAATCTC[-/A]AAATGTAAAATATAT | 2074 |
rs780889430 | in-del | -/A | 6.68014e-05 | 0.00577895 | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517100 | ATTTCATGTAAACTT[-/A]AGTGTTCGAGGCATC | 2074 |
rs780917091 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471978 | GAGTCAAAGACTGCC[A/G]GAACACCCACACTGA | 2074 |
rs780932291 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49497592 | GATTTTCACGCTGAG[C/T]TGAGATCTAGGAGCA | 2074 |
rs780938733 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480094 | GTCCCTGCAGGCTCT[C/T]CTCAGTTCTCACATG | 2074 |
rs780992670 | snp | A/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539616 | GTATCCGTCCTCAGA[A/T]CTCAGAGGTAGGCGG | 2074 |
rs781015386 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504375 | ATTATTTATATTAAC[A/T]ACTATAGAGTTTTGT | 2074 |
rs781029434 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | ERCC6 | GRCh38.p7 | 10:49470749 | TAGCCTCAGATTTCT[C/T]TTCAGATGATGTGGC | 2074 |
rs781059636 | snp | C/G | 1.64732e-05 | 0.0028699 | missense | ERCC6 | GRCh38.p7 | 10:49478380 | TATCTGGCAAAGAAA[C/G]GCTCATCTTGACATC | 2074 |
rs781083294 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523733 | CTGTCGGTATAAAGG[C/T]GACACAGCTCACACT | 2074 |
rs781113329 | snp | C/T | 3.29647e-05 | 0.00405971 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515424 | TTATGACATTCAGCG[C/T]ATCGCGTTTGCTTTC | 2074 |
rs781113838 | snp | A/C | 1.65567e-05 | 0.00287716 | missense | ERCC6 | GRCh38.p7 | 10:49505904 | AAGCTTTTTGAACAG[A/C]AAACCTGGCACTTTA | 2074 |
rs781118377 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49505481 | AAAGTTTTTTATTTC[A/C]ACATAGAAGAAAAAA | 2074 |
rs781128107 | snp | C/T | 1.65307e-05 | 0.0028749 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472328 | GAAAAATTCCCTGCT[C/T]AAGACTCTGGGAACG | 2074 |
rs781179884 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534978 | GCTAGCCCGGGACAC[A/G]GACAAGAGGTCACAC | 2074 |
rs781193747 | snp | A/G | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456043 | AATGTCTTGCATATA[A/G]TATTAAATGAAAAGT | 2074 |
rs781199666 | snp | A/C | 1.65384e-05 | 0.00287557 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516551 | GACATAACCACTCAG[A/C]AAAATAATTCCCAGA | 2074 |
rs781201657 | snp | A/G | 1.76905e-05 | 0.00297404 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515332 | GAGGTGGTGACACCT[A/G]CTATTCAGTGTGATA | 2074 |
rs781207767 | snp | A/G | 0.000116168 | 0.0076204 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516413 | TGGATCCAAATTTGC[A/G]TTGTCAGCAACATGC | 2074 |
rs781210515 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518515 | GAACCACTAAGTCGT[A/G]CGCATTCAAACATGT | 2074 |
rs781212583 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524434 | CTTCTGGAGTTTCTT[C/G]ATGTGCTTTTTCAAA | 2074 |
rs781224749 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467591 | TATTTTTTGACATGG[A/G]GTCTCGCTCTGCTGC | 2074 |
rs781243820 | snp | C/T | 1.8757e-05 | 0.00306237 | missense | ERCC6 | GRCh38.p7 | 10:49461542 | CATCGTGCTTCATGA[C/T]ACTGTGCACGCCAAC | 2074 |
rs781257169 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517432 | ACTCTGTGCACCAAG[G/T]GATAACATGTACCCT | 2074 |
rs781280456 | snp | C/G | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539718 | CAATGGGAGGAAGTT[C/G]AGCTTCGCCTGGGGA | 2074 |
rs781316651 | snp | C/G | 1.66535e-05 | 0.00288556 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516145 | CACCGACACCATATT[C/G]CTCATGTTTAGTATT | 2074 |
rs781332656 | snp | A/C | 3.29506e-05 | 0.00405884 | stop-gained, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524133 | AAGCAGCTTCAGCTT[A/C]TTCCCCAGAACTTGG | 2074 |
rs781335141 | snp | A/G | 1.65869e-05 | 0.00287979 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516050 | AAGTGCAATACTGGT[A/G]AAAAAGTTATTGAAT | 2074 |
rs781338563 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468483 | GAAAACCATTGCTTC[A/C]TATGTTTTGTCATTG | 2074 |
rs781368043 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469473 | ATAGGAGAGTTCTTC[A/G]TATTATTCCAACTGA | 2074 |
rs781424901 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49524029 | ATAATCCCCACAGAC[C/T]GACCTTAACCGCTGC | 2074 |
rs781429074 | in-del | -/AGA | 1.64787e-05 | 0.00287038 | cds-indel | ERCC6 | GRCh38.p7 | 10:49470543 | ATCACCAGATGGCAT[-/AGA]AGTTTTGCCTGTTCC | 2074 |
rs781472671 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | ERCC6 | GRCh38.p7 | 10:49532919 | GACTCTGTAAACAGT[C/T]TTGCTCCTGAGTTTG | 2074 |
rs781475971 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526457 | ATGATTTCTAGTTCT[C/T]TATACATCCTAGATT | 2074 |
rs781494837 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49489194 | TGACCATGAACATTT[C/T]TGATAAAGTAGATGT | 2074 |
rs781507978 | snp | G/T | 1.65548e-05 | 0.002877 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532502 | ATATCCCTGTCATGT[G/T]TTACCACCACTTTGA | 2074 |
rs781525731 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468917 | GCTTGAAGGAGCTCC[C/T]ACCCATGAGGCAAAT | 2074 |
rs781538914 | snp | A/C | 1.64792e-05 | 0.00287042 | missense | ERCC6 | GRCh38.p7 | 10:49459168 | CGGATGAAGAGTCTG[A/C]ATCTTCTGCTCTTCC | 2074 |
rs781586358 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520993 | CAAGGCCCTGCACTG[A/G]ATGAACTTCCCCAAC | 2074 |
rs781663379 | snp | A/G | | | missense | ERCC6 | GRCh38.p7 | 10:49532543 | ATGGGCTGCACTCAC[A/G]TGAGGTCATCCAGGA | 2074 |
rs781663532 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520115 | AAACTGCATCAGCCA[A/G]AAGCTGCAGCCCCAA | 2074 |
rs781688378 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49473515 | GCTGTCTTGAAGCTA[C/T]TGTAGTGGTACCATC | 2074 |
rs781691729 | snp | A/T | 3.29565e-05 | 0.00405921 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473437 | TTTCCCTCCACGTAC[A/T]GCAGCACCACTCAAC | 2074 |
rs781739063 | snp | C/G | 2.89005e-05 | 0.00380124 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488242 | CCAATCCCTCCTAGA[C/G]GGCAAACAGTGGACT | 2074 |
rs781772425 | snp | A/T | 1.65696e-05 | 0.00287828 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524692 | CTGGGTACCAAAAGG[A/T]GTCATCTGGCCAGTG | 2074 |
rs786205166 | in-del | -/T | | | frameshift-variant, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524149 | TGATGATGACTTTTT[-/T]CCCAAGTTCTGGGGA | 2074 |
rs786205167 | in-del | -/G | | | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49483487 | AGATGTTGCTCATTG[-/G]TCATGGAATTTTGAT | 2074 |
rs786205168 | in-del | -/G | | | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49505892 | TTTTCTGTTCAAAAA[-/G]CTTTTTAAGTATGTA | 2074 |
rs786205169 | in-del | -/A | | | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49482857 | CTCAAATAGTTTCGC[-/A]CCCCTCATCGGATCA | 2074 |
rs786205170 | in-del | -/A | | | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49470547 | CAGGAACAGGCAAAA[-/A]CTTCTATGCCATCTG | 2074 |
rs786205171 | in-del | -/A | | | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49470424 | TGGAAAATAATTTTT[-/A]TAAGCACAAGTCAAA | 2074 |
rs786205172 | in-del | -/GGGCTGGCTGCTTAAGGTCCACCTTA | | | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49470352 | AACATCTGAGACCAA[-/GGGCTGGCTGCTTAAGGTCCACCTTA]AGCAAAAGCCTAAGA | 2074 |
rs786205173 | in-del | -/T | | | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49470347 | CTGAGACCAAAGCAA[-/T]AAGCCTAAGAACTCT | 2074 |
rs786205174 | snp | C/T | | | stop-gained | ERCC6 | GRCh38.p7 | 10:49461431 | CTGAGGCTCTCTCGT[C/T]AGCGGTGTCTGGGAG | 2074 |
rs786205175 | in-del | -/A | | | frameshift-variant | ERCC6 | GRCh38.p7 | 10:49460428 | TTGGTAAGAAAAGGA[-/A]TTCTAACTTCTCTGT | 2074 |
rs796080242 | snp | C/T | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539182 | CGTGGTTTGGAGGGA[C/T]GGGCTCAGCAGCGCC | 2074 |
rs796250214 | in-del | -/AATGC | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517214 | GTCAAACCCATAACT[-/AATGC]AATAATAATACTTTC | 2074 |
rs796268799 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533586 | CCAGGGAAACACAGC[A/G]AGCTCAGGACTTCGA | 2074 |
rs796306948 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506700 | ATATATTTCATCTAA[A/G]TATCTGAAAGTCTTA | 2074 |
rs796333004 | snp | C/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539962 | TCCATAACATCATCT[C/T]ATTCCTCCTGTCAGC | 2074 |
rs796435597 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49460897 | CATCTCTAAAAAAAG[-/A]AAAAAAAAAAAGGAA | 2074 |
rs796507234 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484291 | CTCAAAAAAAAAAAA[-/A]GAAAAAAAAAAAAAG | 2074 |
rs796529928 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526127 | TATTTTTATATATAT[A/T]TATATATATATATAT | 2074 |
rs796556751 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480767 | TGCACTGAGGAAGAC[A/C]CATCACTTCTGTGAT | 2074 |
rs796639457 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495578 | CCACACACTAGAAAT[C/G]TCACTGCCGATATCC | 2074 |
rs796688071 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49480363 | ATACCTTCATGGGAA[C/G]GTTCTGGTTTCTAGC | 2074 |
rs796786626 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495400 | CTCCACTCCCTTTTC[C/T]TGCCCCACAAAGATG | 2074 |
rs796871636 | in-del | -/TATATATTTATATATTTATATATTTTTATA | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526092 | GGTTTTATTTATATT[lengthTooLong]TATATATATATATAT | 2074 |
rs796894424 | in-del | -/TAAA | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518906 | CTCAGAGTTACTCAT[-/TAAA]GTAAAAAAGGTAAAA | 2074 |
rs796897981 | multinucleotide-polymorphism | AT/GA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49531070 | ATTTAGATCAGCTCA[AT/GA]CCCATTTGTAAGCTG | 2074 |
rs796935210 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538892 | CGCGGGGCCGCGGCC[-/C]GCCCGAGAAGCCTGA | 2074 |
rs797021174 | snp | G/T | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456085 | TAAGGATGGTATAAG[G/T]CCATTAATATAAATT | 2074 |
rs797045562 | in-del | -/T | | | frameshift-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524579 | CAAAACTGTCTTTTG[-/T]AAAGGAAGAAGCAAG | 2074 |