SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs734907 | snp | A/G | 0.00332778 | 0.0406548 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480160 | GTCTATATTTGGGCT[A/G]CTGACATGCTCCCCA | 2074 |
rs912470 | snp | A/C | 0.128976 | 0.218754 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480609 | gacatgttctcaaat[A/C]atttttctataaatg | 2074 |
rs932735 | snp | A/C | 0.473266 | 0.112482 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467878 | tgtctggaacccaat[A/C]aaaaattacTggctg | 2074 |
rs958967 | snp | A/G | 0.179425 | 0.239831 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502574 | AGCTCAGAATGGTTA[A/G]GTAACTTGCCAAAGG | 2074 |
rs971026 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463700 | cagtgtaggaaagac[G/T]catcttcataattaa | 2074 |
rs971667 | snp | A/G | 0.29789 | 0.24537 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497048 | CCAGCTACAGTCACT[A/G]TCCCTGCCCTTCAAC | 2074 |
rs973808 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498403 | TTCTGTAAGACATAA[A/G]TATAGAGAACTCCCA | 2074 |
rs1012553 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532097 | TTCAGATTTGCATTT[C/T]TAGAAATAATAAAGA | 2074 |
rs1012554 | snp | A/G | 0.483563 | 0.0891524 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531511 | GGCTGGTGGCATGTG[A/G]TGTCTCAGCCAGTAA | 2074 |
rs1018603 | snp | A/C | 0.215446 | 0.2476 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520325 | GGGAAGCTTTGCTCT[A/C]GTCTGTGCTCGTTGC | 2074 |
rs1126112 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533037 | CATTGTAGTTCTTAA[A/G]TATTTTATAATTAGA | 2074 |
rs1917801 | snp | C/T | 0.232943 | 0.249417 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536260 | CACTGTAGCTGTCTC[C/T]CTGCCAGAGGCAAGC | 2074 |
rs1917802 | snp | A/G | 0.237303 | 0.249677 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536124 | CACTGAAACTTTTTT[A/G]TTTTTTCGAGACAGA | 2074 |
rs1924488 | snp | A/G | 0.370772 | 0.218893 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496787 | CACTCCAGCCTGGGC[A/G]ACAAGAGCGAGACTC | 2074 |
rs1964145 | snp | A/C | 0.0905309 | 0.192535 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533205 | AAATGCAGTATCATC[A/C]ACAAAGGACATTTAG | 2074 |
rs2104346 | snp | C/T | 0.128976 | 0.218754 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464555 | CATGAAGGTCTCTGA[C/T]ATGCCCTGCAGACAT | 2074 |
rs2209281 | snp | A/G | 0.481396 | 0.0946345 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465332 | TCCTAGATACAATAG[A/G]GTTACAGGCATTGGG | 2074 |
rs2228524 | snp | C/G | 0.424235 | 0.179283 | ERCC6 | 10 | allele_origin=G(germline)/C(germline) | 10:49532830 | GGTGGAGGAGTACCT[C/G]TCCTTTCGTTCTGTG | 2074 |
rs2228525 | snp | C/T | 0.0103388 | 0.0711514 | missense | ERCC6 | GRCh38.p7 | 10:49472913 | ACCCAAGCACGGACA[C/T]GCAGGTTTGTTTTTA | 2074 |
rs2228526 | snp | A/G | 0.341578 | 0.232623 | ERCC6 | 10 | allele_origin=G(germline)/A(germline) | 10:49470671 | AAAGATGACCCTCAC[A/G]TGAGTAGTAATGTAA | 2074 |
rs2228527 | snp | A/G | 0.343574 | 0.231827 | ERCC6 | 10 | allele_origin=G(germline)/A(germline) | 10:49470323 | AACTCTAAGCATTGC[A/G]GAGACGCCAAGTTTG | 2074 |
rs2228528 | snp | A/G | 0.314901 | 0.241429 | ERCC6, PGBD3 | 10 | allele_origin=G(germline)/A(germline) | 10:49524234 | ACCTGTCTGGAGATG[A/G]TACTGACTATGAGCT | 2074 |
rs2228529 | snp | A/G | 0.340775 | 0.232937 | ERCC6 | 10 | allele_origin=G(germline)/A(germline) | 10:49459059 | AAAGCGGGCACCTGC[A/G]GGAAGCTTCTGCCCT | 2074 |
rs2229760 | snp | C/T | 0.446871 | 0.154084 | ERCC6 | 10 | allele_origin=T(germline)/C(germline) | 10:49472987 | GACCACGCGGGTGGG[C/T]GGCTTAGGTGTCAAC | 2074 |
rs2229761 | snp | C/G | 0.00444633 | 0.0469403 | missense | ERCC6 | GRCh38.p7 | 10:49461413 | CGGTGTCTGGGAGCA[C/G]TGTCTGGTGTTCCCA | 2074 |
rs2274097 | snp | C/T | 0.0216935 | 0.101863 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49471035 | AATGATCTCTATGAG[C/T]TATTTACTCTGACTA | 2074 |
rs2281792 | snp | C/T | 0.389527 | 0.207442 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519310 | CTGTGGGCAAGCCAA[C/T]TAACTGGAGGGGCCG | 2074 |
rs2281793 | snp | C/T | 0.389715 | 0.207315 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519496 | GAGGGAGCCTTCAAA[C/T]CATGCAGAGGAACCA | 2074 |
rs2281794 | snp | C/T | 0.289942 | 0.246789 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520374 | GGGCAGCAACTTAAA[C/T]AGTAACTGCCGATAC | 2074 |
rs3219688 | microsatellite | (CA)15/16/17/18/19 | 0.7451 | 0.109864 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537534 | atatatatatatata[(CA)15/16/17/18/19]aaatataattGTGGT | 2074 |
rs3750745 | snp | G/T | 0.373397 | 0.217424 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538877 | GGGCCGCGGCCCCGC[G/T]CCTTGGCCTCGCCGT | 2074 |
rs3750746 | snp | C/T | 0.353587 | 0.22753 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538810 | GGTCTTAGGGCCAAG[C/T]GCCCGCTTCCGGCGG | 2074 |
rs3750747 | snp | C/G | 0.381891 | 0.212379 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538806 | TTAGGGCCAAGTGCC[C/G]GCTTCCGGCGGCCTC | 2074 |
rs3750748 | snp | A/G | 0.284995 | 0.247539 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521368 | GTGATGTGGGTTCCC[A/G]GTGAGCACCTACATG | 2074 |
rs3750749 | snp | C/T | 0.213756 | 0.247359 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476182 | AGCTGGAGAAATGAA[C/T]TGTGGACCAAGAGAA | 2074 |
rs3750750 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476161 | ACCAAGAGAAGTGAG[A/G]GAGGAAAAGAAACTA | 2074 |
rs3750751 | snp | A/G | 0.208169 | 0.246476 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457882 | GCGACGGGCTTTCTT[A/G]TTTCTGCGGTTTGGA | 2074 |
rs3763728 | snp | A/C | 0.422158 | 0.181278 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540304 | CACCTGTAATCCCAG[A/C]ACTCTAGGAGGCCGA | 2074 |
rs3763729 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-5-prime | ERCC6 | GRCh38.p7 | 10:49539461 | AGTCGTGGGAGACAA[C/T]AAGAGAGGTCACAGC | 2074 |
rs3763730 | snp | A/C | 0.479421 | 0.0993283 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511454 | TGACGTGACAGAGTG[A/C]GACTTTGTCTCAAAA | 2074 |
rs3793784 | snp | C/G | 0.362523 | 0.223246 | ERCC6 | 10 | allele_origin=G(germline)/C(germline) | 10:49539493 | AAGCAGGACAGCTCT[C/G]CATCCTTCCCGTGTT | 2074 |
rs3793785 | snp | G/T | 0.100588 | 0.200439 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536528 | GCTTTGTGGGATATT[G/T]TGTCTGTAATCCACT | 2074 |
rs3793786 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535042 | AAATCTCAGTTCCTC[C/T]GTGATATTTCTTGGG | 2074 |
rs3793787 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525281 | ATAGCTGCAGGTGAC[C/T]GGTAACTGCCATGCT | 2074 |
rs3793788 | snp | A/T | 0.417359 | 0.185718 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502806 | TTGCTGTGGGGACTG[A/T]CCTGTGCAGTATCAG | 2074 |
rs3810944 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461116 | CAACACCATCTCTCA[A/G]ATAAAACCAATCACT | 2074 |
rs3810945 | snp | C/T | 0.284995 | 0.247539 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461123 | ATCTCTCAAATAAAA[C/T]CAATCACTTCTCCTG | 2074 |
rs3838760 | in-del | -/T | 0.359787 | 0.224604 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502954 | GCACATCAGTTTTTT[-/T]GGAGAGCTTTTTGCA | 2074 |
rs3940160 | snp | A/G | 0.413083 | 0.189483 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464180 | aagttcctcatctcc[A/G]tctgagaccacctca | 2074 |
rs4240505 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470020 | TGACATTTTAAAAAT[C/T]GTATTTACACCTCTT | 2074 |
rs4240506 | snp | A/G | 0.479583 | 0.0989539 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482963 | TGATGCAAGAATGAT[A/G]AGTAAATGTGTAAAT | 2074 |
rs4240507 | snp | A/C | 0.483563 | 0.0891524 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493931 | GCCCACACAGCAGTG[A/C]CAGCTTGTACACTGT | 2074 |
rs4240508 | snp | A/G | 0.483563 | 0.0891524 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494329 | CTTATAGTATTTTCT[A/G]TATGGTCCTGTTCTA | 2074 |
rs4240509 | snp | A/G | 0.132409 | 0.220618 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494422 | TTTTTAAAAATTATG[A/G]TGAACATTTTTCTAG | 2074 |
rs4240510 | snp | C/T | 0.212728 | 0.247206 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503394 | AGATTTTTTTTAATG[C/T]CATTTTCTTAGTGCT | 2074 |
rs4253001 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539905 | CATTTCCCTATTGTC[C/T]GACTTCAGGCTTCCA | 2074 |
rs4253002 | snp | A/G | 0.0221141 | 0.102801 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539292 | CTGCCTTGCCAGCAG[A/G]GTATTTTTCGCTAGG | 2074 |
rs4253003 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539164 | CCTCCAAACCACGTG[A/G]TCTTGCCCGTGCTTA | 2074 |
rs4253004 | snp | A/C | 0.21845 | 0.248001 | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49539034 | GCAGGCGCCACGGCC[A/C]GTCGAGCTGGGTTCC | 2074 |
rs4253005 | snp | G/T | 0.0788843 | 0.182262 | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49539025 | ACGGCCCGTCGAGCT[G/T]GGTTCCAAGGCGGCT | 2074 |
rs4253006 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49538969 | TGTGGGCGCTCGCGC[A/G]GCCCTGGGTGAGTGT | 2074 |
rs4253007 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538875 | gccgcggccccgcgc[C/T]TTGGCCTCGCCGTGG | 2074 |
rs4253008 | snp | C/G | 0.0799831 | 0.183287 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538730 | TTGAGTCCCTGGCCG[C/G]CCAGCGACCCAGCTA | 2074 |
rs4253009 | snp | A/G | 0.488965 | 0.0734569 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533383 | AACATCGCTGTTCCT[A/G]TGCATTACAGTTGAT | 2074 |
rs4253010 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533358 | GTTGATCTTGCCACT[A/G]TATTATAAATCATTT | 2074 |
rs4253011 | snp | C/T | 0.275197 | 0.248727 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533134 | AGAAGATACGTTGTC[C/T]CTTTTTAGTAAATTA | 2074 |
rs4253012 | snp | C/G | 0.000217008 | 0.0104143 | utr-variant-5-prime | ERCC6 | GRCh38.p7 | 10:49532975 | TTTTCCTTTTAGGTA[C/G]TCTGTAGAGAATGCC | 2074 |
rs4253013 | snp | A/G | 0.20962 | 0.246717 | ERCC6 | 10 | allele_origin=G(germline)/A(germline) | 10:49532554 | GTATCGGTCGGTCCT[A/G]GATGACCTCACGTGA | 2074 |
rs4253014 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49532216 | CAGGTGTTTCCTATT[A/C]GAGATGCCAGGAATA | 2074 |
rs4253015 | snp | A/G | 0.100231 | 0.200173 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531914 | GAGGACAGGAGAGGG[A/G]AAGTGGGAGGGGTTG | 2074 |
rs4253016 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531870 | TTGCTGCTTGGCCCC[C/T]GTTGGGCAGTGTTCT | 2074 |
rs4253017 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531869 | TGCTGCTTGGCCCCC[A/G]TTGGGCAGTGTTCTG | 2074 |
rs4253018 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531814 | AAGGCGAGGGCTGAA[C/T]GGGATGGAGGATGGA | 2074 |
rs4253019 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531728 | GTTGTTGGTACTTCA[A/G]AGACATGTTTTCTGC | 2074 |
rs4253020 | snp | A/G | 0.00360359 | 0.0422943 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531538 | GGGTCTCCATGCAGA[A/G]TGATGCTAGATGGCT | 2074 |
rs4253021 | in-del | -/GTGCT | 0.149297 | 0.228821 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531325 | GCACCACAAAGTTTA[-/GTGCT]GTAGTAAGTGAATCT | 2074 |
rs4253022 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531282 | GAAGAAAAATATTGT[C/T]GCAGATGTGTGATTT | 2074 |
rs4253023 | snp | C/G | 0.234401 | 0.249513 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531217 | TCCAGACTTTGGAAG[C/G]CTTCCGTAACGGGCT | 2074 |
rs4253024 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531212 | ACTTTGGAAGGCTTC[C/T]GTAACGGGCTTAAAA | 2074 |
rs4253025 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531164 | TTTCATGTAAAAGGA[C/T]AACTTATTGCACATT | 2074 |
rs4253026 | snp | C/T | 0.12932 | 0.218944 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531070 | GCTTACAAATGGGAA[C/T]GAGCTGATCTAAATC | 2074 |
rs4253027 | snp | A/G | 0.0460249 | 0.144548 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49530735 | AGATTCTGTAAAACG[A/G]CAGAAGTATAATAAG | 2074 |
rs4253028 | snp | C/T | 0.275732 | 0.248672 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530443 | TTACATCCCGACAAA[C/T]CCATCGTAAATTGAA | 2074 |
rs4253029 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530410 | tattgttagtcaaaa[A/G]tgcattaaatacact | 2074 |
rs4253030 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530401 | tcaaaaatgcattaa[A/G]tacactgaaaaacct | 2074 |
rs4253031 | snp | C/G | 0.00336134 | 0.0408579 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530005 | AGAGCTTGGCCCTTC[C/G]TCCCACCTTGGGTGT | 2074 |
rs4253032 | snp | C/T | 0.00447425 | 0.0470862 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529887 | TATGAAGTTTGAAAC[C/T]TTTTTTAAGGATTTA | 2074 |
rs4253033 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529849 | CTTTGTGAGGTCTGA[A/G]ACATTTTTTATGATT | 2074 |
rs4253034 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529622 | ACTCACCAGTCTGTT[A/G]CCTGCACTACCCCAT | 2074 |
rs4253035 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529173 | CCAGGTACCACAAGC[C/T]CAGTTCATTGGGCCT | 2074 |
rs4253036 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529161 | AGCCCAGTTCATTGG[G/T]CCTCCCCAGTGAAGC | 2074 |
rs4253037 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529096 | AGGGAACAAGACAAA[A/G]AGGAGTCTGGCGTGG | 2074 |
rs4253038 | snp | C/T | 0.373799 | 0.217195 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528933 | TTATTTCTTATCTTA[C/T]GGCCTGTTGACTTCC | 2074 |
rs4253039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528738 | TGCAGGCATGCCTGT[C/G]TGCTGGGAATATTCA | 2074 |
rs4253040 | snp | A/T | 0.289424 | 0.246872 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528282 | AGTGTCAAAACAGAT[A/T]TAGGAAAATTTTATT | 2074 |
rs4253041 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528274 | AACAGATTTAGGAAA[A/G]TTTTATTCTCTACAC | 2074 |
rs4253042 | snp | A/G | 0.275197 | 0.248727 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525181 | TGTCTCTTGAATTTA[A/G]GTCCATCTGAATGTT | 2074 |
rs4253043 | snp | G/T | 0.289942 | 0.246789 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525029 | TTTGGATGGCAGAGA[G/T]TATATTTATAGTGAA | 2074 |
rs4253044 | snp | C/T | 8.23649e-05 | 0.00641683 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524545 | TAATAAAAGAGCAGC[C/T]AGAAAAGCTCCAGCC | 2074 |
rs4253045 | snp | A/G | 0.0048893 | 0.0492011 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524284 | Agaggaggaggaaga[A/G]gaggaagatgacgag | 2074 |
rs4253046 | snp | A/C | 0.00338815 | 0.0410194 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524156 | AGGAGATTGATGATG[A/C]CTTTTTCCCAAGTTC | 2074 |
rs4253047 | snp | A/G | 0.0187357 | 0.0949569 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524093 | AAGGAGGAGGAGGAG[A/G]TCGGAAAGTGGGAAG | 2074 |
rs4253048 | snp | A/G | 0.0139853 | 0.0824443 | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524035 | TTATAAGCAGCGGTT[A/G]AGGTCGGTCTGTGGG | 2074 |
rs4253049 | snp | C/T | 0.275464 | 0.2487 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523839 | TGCTGGCCCCAAATG[C/T]ATGTACTTCTAGGTC | 2074 |
rs4253050 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523802 | TGGATTTGGAGGCAA[C/G]TCTAAGATGAAAAAC | 2074 |
rs4253051 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523796 | TGGAGGCAAGTCTAA[A/G]ATGAAAAACTTAAGG | 2074 |
rs4253052 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523687 | TATCAGGAAAAAGAA[A/G]AGGGTGAATTAATGC | 2074 |
rs4253053 | in-del | -/A | 0.0116955 | 0.0755709 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523513 | TAGTCATCTGCATAA[-/A]TTATAAGCCACCATC | 2074 |
rs4253054 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523055 | GTGAAGGTTGACCTG[A/G]TGTTTTTTCTTGTTA | 2074 |
rs4253055 | snp | C/T | 0.275999 | 0.248644 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520281 | ATTATGCAGTGTCAC[C/T]GGGAGCCCCTAACAC | 2074 |
rs4253056 | snp | A/C/G | 0.00716266 | 0.059414 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520209 | CAGGACTTTTAAAAA[A/C/G]TGTTCCCAGATGGCT | 2074 |
rs4253057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519939 | GAAACACCTTCAGAG[A/G]GTAGGGGCCTGGGCT | 2074 |
rs4253058 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519905 | CGTGGGGAGTCTGAG[A/G]CAGCAGGTGCAGAGT | 2074 |
rs4253059 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519848 | CTTTGGCTGAGCTCC[C/T]GCTGACTCTGAGGGG | 2074 |
rs4253060 | snp | A/G | 0.289942 | 0.246789 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519741 | CAGTTGGGAAGCATT[A/G]TTGGTAAGGATGTTG | 2074 |
rs4253061 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519675 | GCCCACACTCAGCAA[A/G]TAATTGCCTCTGGGA | 2074 |
rs4253062 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519582 | CTTCAGTAGGCGGTG[C/T]CTGAGTCTCCTCAGA | 2074 |
rs4253063 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519243 | TGGGCCCTCTACATA[C/T]ATGTTTCCTTCCCTT | 2074 |
rs4253064 | snp | C/G | 0.00338409 | 0.040995 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519226 | TGTTTCCTTCCCTTT[C/G]TGGGATTGAGTAGAA | 2074 |
rs4253065 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519138 | CCACCTCCATTGGAC[C/T]GAAAACCAAACCAAA | 2074 |
rs4253066 | in-del | -/TAAA/TTTA | 0.0182019 | 0.0936463 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518907 | TTTTTACCTTTTTTA[-/TAAA/TTTA]CATGAGTAACTCTGA | 2074 |
rs4253067 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518844 | TGTAAGTCTTACAGA[A/G]TGTCTTCTAATAGTC | 2074 |
rs4253068 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518719 | GGGAGGGTTGGGTTG[C/T]GCACATCCACTGTTC | 2074 |
rs4253069 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518547 | GCGGGAGTGGTGCAC[A/G]AGAACAATGATGGCT | 2074 |
rs4253070 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518423 | GACTTTGAGCCCAGA[A/G]AGATGAAGTCATTTG | 2074 |
rs4253071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518297 | CAGCAGACTCGGACA[A/G]GCATTGTTTCAGTGC | 2074 |
rs4253072 | snp | A/G | 0.00345405 | 0.0414137 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515970 | AGGATCACATTGACA[A/G]AGTTCCACTGGAATC | 2074 |
rs4253073 | snp | C/T | 0.168632 | 0.236388 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515638 | TTGTTCTGTTTCGAA[C/T]TGGTCTTACAAAATG | 2074 |
rs4253074 | snp | A/T | 0.0517044 | 0.152246 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515271 | TGTACAGTGTAGCAG[A/T]GGTTTTGCCTAGTGT | 2074 |
rs4253075 | snp | A/G | 0.0543475 | 0.155628 | intron-variant, utr-variant-3-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49515241 | TTCCAATTTTGGAAC[A/G]TCACATAACAATGGA | 2074 |
rs4253076 | snp | A/G | 0.00336134 | 0.0408579 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514998 | TTCTTGGCTCTGGGC[A/G]TAATTGTCTATATCA | 2074 |
rs4253077 | snp | G/T | 0.190833 | 0.242898 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514923 | TTCATCTGCTCAGAT[G/T]TGCCAATTAAGTTTA | 2074 |
rs4253078 | snp | C/G | 0.0391387 | 0.134304 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514826 | GACTAATCTGTAAGG[C/G]ATTCTTAGCTGTCTG | 2074 |
rs4253079 | snp | A/C | 0.21303 | 0.247251 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514779 | ATACTACAGAATGCA[A/C]ACTATATTAAATACC | 2074 |
rs4253080 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510035 | TCTCTGTCTGCATCT[C/G]ACTGGAATTGTAGGT | 2074 |
rs4253081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509869 | CTGTGACTATTACGT[C/G]TGTGGATTTTTTAAA | 2074 |
rs4253082 | snp | A/G | 0.417196 | 0.185864 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509540 | AATTGAGATATTCCA[A/G]CAGGTACCATCTGAA | 2074 |
rs4253083 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508860 | GCACGTTTCTGTGTA[C/T]GTGCAGATGAACCTG | 2074 |
rs4253084 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508836 | GAACCTGGTTCTCCC[C/T]CTTTCCCTAGTGTGT | 2074 |
rs4253085 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508576 | TGCAGGCAATAATGA[C/T]TTTCCCCACCACTTT | 2074 |
rs4253086 | snp | C/G | 0.00682586 | 0.0580201 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508376 | AAACTGAATCTTGTC[C/G]ATGCAGAGTGATGTG | 2074 |
rs4253087 | snp | A/G | 0.146314 | 0.227484 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508294 | TCATCATATATCAAT[A/G]AAGTTTAAAAAGTGA | 2074 |
rs4253088 | snp | A/G | 0.00365629 | 0.0426002 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508054 | CATAGTTTTGATACC[A/G]AGGACTCTCTCATTA | 2074 |
rs4253089 | in-del | -/AAGAATTCAGATATGTGTATCAGGAAAGTGTATATATATC | 0.237188 | 0.249671 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507920 | AAGTGTATATATATC[lengthTooLong]TGTTCAGTTTCTAAG | 2074 |
rs4253090 | in-del | -/G | 0.0121208 | 0.0768991 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507893 | AAGTTTTGATAGTAA[-/G]GGATACCTATATGCc | 2074 |
rs4253091 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507741 | gccagtagtagtata[A/T]cctcccgactccttc | 2074 |
rs4253092 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507670 | attaccccagggtgg[G/T]GTTGAAGGGACAGAA | 2074 |
rs4253093 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507226 | TTGTTACCTTGAAGA[A/G]TTGAAATTTTCAACA | 2074 |
rs4253094 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507186 | TTTATCAGAGGATGT[G/T]CTTTAAGGTCCACCA | 2074 |
rs4253095 | snp | C/T | 0.290201 | 0.246747 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507149 | ACCTACATACTAGCA[C/T]TGGGCTCTGTGTGGT | 2074 |
rs4253096 | snp | A/T | 0.0524604 | 0.153226 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506680 | ATGAAATATATTTCC[A/T]TCTGAAATATAAGTG | 2074 |
rs4253097 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506510 | TAATGTGAACCTGAT[C/T]CAGTGATTTTGACCC | 2074 |
rs4253098 | in-del | -/AAAAT | 0.200801 | 0.245111 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506412 | ATAGTAATTATAAAT[-/AAAAT]CTATTTTTTGTTACA | 2074 |
rs4253099 | snp | C/T | 0.0998734 | 0.199905 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506389 | TGTTACATAGTATTG[C/T]GGTTGTGAAGACACT | 2074 |
rs4253100 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506320 | TAATTTCATGTCTTA[C/T]GAACCAGCAGAGAAA | 2074 |
rs4253101 | snp | A/C | 0.297636 | 0.24542 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505013 | TTTGGTCTCCTTTAT[A/C]GATTCAGCTGTCAGC | 2074 |
rs4253102 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504861 | AGTTTTTTTATCCCA[C/T]TAAACATTATAGAAA | 2074 |
rs4253103 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504832 | AAGCCAAACTCTAAA[C/G]ATGTGAAGTGACTTG | 2074 |
rs4253104 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504614 | GAAACAAGCCAAATA[C/T]CATCAGTGTTGTACT | 2074 |
rs4253106 | snp | A/G | 0.297128 | 0.245518 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504127 | TTTTTTACTGTATTT[A/G]CTGCATTCTGTGGAA | 2074 |
rs4253107 | snp | C/G | 0.0111728 | 0.0739025 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504099 | GAATTGAATTGACAG[C/G]GTATAGAGTTGTACA | 2074 |
rs4253108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504019 | ATAGTGTTTAACTTT[C/T]AAATTTCTGTTTTGA | 2074 |
rs4253109 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503734 | ATTTTGAAAACTAGA[A/T]TCTATAATATGTTTT | 2074 |
rs4253110 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503567 | TCATCTACCAGCTGT[A/G]TGGCTAGTGCTTTTA | 2074 |
rs4253111 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503523 | TTTCCTTTAAATACC[A/G]TCTGAGGGCCTTCGT | 2074 |
rs4253112 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503510 | CCATCTGAGGGCCTT[C/T]GTGTATTGTGTGGAA | 2074 |
rs4253113 | snp | C/T | 0.00338409 | 0.040995 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503442 | TAGTTTTTGGGGATC[C/T]TGCTAGAGATATGAC | 2074 |
rs4253114 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501575 | GTTTCTTCCACTCTC[C/T]GAAAATTTTTTTGTA | 2074 |
rs4253115 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501021 | TTTCCCCCAGAAAGT[A/G]AGTAAAAAATAGTAA | 2074 |
rs4253116 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500015 | TGAGTGTGCATGATA[A/G]CATTTCTAGATAGCT | 2074 |
rs4253117 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500014 | GAGTGTGCATGATAG[C/G]ATTTCTAGATAGCTT | 2074 |
rs4253118 | in-del | -/TT | 0.0410537 | 0.137264 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499987 | AGCTTGCTCTCTCTC[-/TT]GTTTTTGAATGAAGT | 2074 |
rs4253119 | in-del | -/T | 0.379746 | 0.213696 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499924 | CCAATCTATGAACTT[-/T]ATGTAATAAATTCTA | 2074 |
rs4253120 | snp | C/T | 0.146314 | 0.227484 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499893 | ATGCCAAAACGTAAG[C/T]GACTACCTAAAATGG | 2074 |
rs4253121 | snp | C/T | 0.29432 | 0.24604 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498941 | TGGTAACTAGACAAC[C/T]CCAAACTCCTCCAAA | 2074 |
rs4253122 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498848 | TTCTTTTCTTTGCTT[C/T]CCTTCCTATTATCAT | 2074 |
rs4253123 | snp | A/G | 0.00349039 | 0.0416295 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498565 | GTGGCTTGTGAGAAT[A/G]TGGTGCTGCACCACA | 2074 |
rs4253124 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494505 | GGAATGCATGTTGAG[A/C]CAATGGCCACAACCA | 2074 |
rs4253125 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494178 | atcatacaatgtgtg[C/T]agagttggattcaga | 2074 |
rs4253126 | snp | A/C | 0.0901694 | 0.192235 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494144 | AGGCAGTGCCTCTAA[A/C]CACTGGCCCATGCTT | 2074 |
rs4253127 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493956 | TCTTGATTTTGCTGC[C/T]GAACTACCTGCCCAC | 2074 |
rs4253128 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493881 | GAGAACACTCGCTCG[C/G]ATGCTCCTCCATGGT | 2074 |
rs4253129 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493811 | AGGACAGGCTGCAGT[A/T]AGTGAAGACTGGCTG | 2074 |
rs4253130 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493769 | TCTGTCCCCTGGTAG[A/C]CATGTCACCTGGGCC | 2074 |
rs4253131 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493511 | TTATGTTACTATAGA[A/T]GTTATATCTCTTAAT | 2074 |
rs4253132 | snp | C/T | 0.197869 | 0.244529 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493110 | CACAAAAAGGTAACA[C/T]AATATTTCAGTACCT | 2074 |
rs4253133 | snp | C/T | 0.0104221 | 0.0714312 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493091 | ATTTCAGTACCTTTT[C/T]GTTTTGTTTTAATGC | 2074 |
rs4253134 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492920 | ATAGGTCTTATTGTT[A/C]TAACAGTCTGTGGTG | 2074 |
rs4253135 | snp | A/G | 0.00357781 | 0.0421438 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492703 | AATGCATTTGTTAGT[A/G]TGCATTTAACCTTCC | 2074 |
rs4253136 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492585 | TTCACTTAGAGTTTG[A/G]TAATATCACAGTATC | 2074 |
rs4253137 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492396 | AATAAATAATAATCA[C/T]GCAGTTTCACTGTGA | 2074 |
rs4253138 | snp | A/G | 0.290201 | 0.246747 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492289 | CTTGAGTTCGTTCTC[A/G]GGGCCCAGGAAAGCA | 2074 |
rs4253139 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492219 | GTCAGATGCACGGGG[A/G]CCACGAAACTCCAGG | 2074 |
rs4253140 | snp | C/T | 0.00336134 | 0.0408579 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492215 | GATGCACGGGGACCA[C/T]GAAACTCCAGGATTC | 2074 |
rs4253141 | snp | C/T | 0.00338409 | 0.040995 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492181 | TTGTGTTTGTGTTCA[C/T]GGAAAAGCAAACTTT | 2074 |
rs4253142 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492142 | GTGACTCAGAAAAAT[A/C]TATGGTTTGGTAGCA | 2074 |
rs4253143 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492006 | AATAAATTAGGGTAA[A/G]TGCTGTGAGTTATAA | 2074 |
rs4253144 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491890 | TCCTGTCACTACCCT[C/T]GTAAAACATTTGTGG | 2074 |
rs4253145 | snp | C/T | 0.284995 | 0.247539 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491790 | TCATTAGCTGATGTT[C/T]GTCTTATAAAGGCAA | 2074 |
rs4253146 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491722 | TAGTAAAGTGTGTGT[A/G]TTGGACACCTTCACC | 2074 |
rs4253147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489376 | ggttaatatgtatgt[A/G]tgaagagcttagtgt | 2074 |
rs4253148 | snp | C/T | 0.00692033 | 0.0584147 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489104 | CAGTGAAGTGCAGGG[C/T]GTGGTTAAAAAAGCA | 2074 |
rs4253149 | snp | A/G | 0.0125781 | 0.0782997 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489028 | tgggaggctgaggcc[A/G]gcggatcatgaggtc | 2074 |
rs4253150 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489023 | ggctgaggccggcgg[A/T]tcatgaggtcagaag | 2074 |
rs4253151 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488869 | gtgaacctgggaggc[A/G]gaacttgcagtgagc | 2074 |
rs4253153 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487768 | CTATACCTATAATAA[C/T]ATTTAGAATTTTCCA | 2074 |
rs4253154 | snp | A/C | 0.00332778 | 0.0406548 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487599 | TTGGCTTCTAAAGGT[A/C]GCAGGTCTGACCAGG | 2074 |
rs4253155 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487595 | CTTCTAAAGGTCGCA[A/G]GTCTGACCAGGTGAG | 2074 |
rs4253157 | snp | G/T | 0.0110494 | 0.0735024 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486874 | AGTTTTGAAAACAGG[G/T]TTTGCTAGCCTTGTA | 2074 |
rs4253158 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486831 | ATCCATTCTTTTTCT[A/G]TATTTTGGAACAATT | 2074 |
rs4253159 | in-del | -/TT | 0.0112991 | 0.0743093 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486602 | TATTGGTTAACACTT[-/TT]GTATTCTCTACATCT | 2074 |
rs4253160 | snp | A/T | 0.370974 | 0.218781 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485920 | TCTCTTTTAAACAGA[A/T]GGCTAGGTTTTTGCC | 2074 |
rs4253161 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483687 | GGCTGTATTAGTCAG[C/T]GTTTACTACTTGCCA | 2074 |
rs4253162 | snp | A/G | 0.16853 | 0.236353 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483314 | CAAGGGAGATTTCCA[A/G]GTGGAGAAGAATAAT | 2074 |
rs4253163 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483247 | TTATTGAATCTTTCC[A/T]TGTGCCAACTGCACA | 2074 |
rs4253164 | snp | A/C | 0.067446 | 0.170804 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483113 | GGGGCCAGTTGTTAG[A/C]ATGTAACCAAACCCA | 2074 |
rs4253165 | snp | A/G | 0.293294 | 0.246223 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482991 | AATGTGTATGTTTTG[A/G]AGAGTACCAAAATGA | 2074 |
rs4253166 | snp | A/C | 0.298144 | 0.245321 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481971 | GCAGGACTCTGGAGG[A/C]TGCTGGTTCTCAGGG | 2074 |
rs4253167 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481894 | TGACCTGCAGGAACC[A/G]CTGGGGTGAGGGCCA | 2074 |
rs4253168 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481707 | CTGAGGTTTCAGGCC[C/T]GGGTGCCTGATGGAA | 2074 |
rs4253169 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481539 | CATGGCTGAGCCAGG[G/T]ATGAGACCTTCCACC | 2074 |
rs4253170 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481512 | CACCAAAAGGGAAGC[G/T]CTCGTATTTTGGAGT | 2074 |
rs4253171 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481485 | GAGTATTTAATTAGA[A/G]AAAGAATTTTAGACC | 2074 |
rs4253172 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481463 | TTTTAGACCTTTAAG[A/G]TTAAAAGATTGTCAA | 2074 |
rs4253173 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481342 | TACCATTCTTTTTTT[A/T]AAAAAAAtttatttt | 2074 |
rs4253174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481275 | tttaaaagaacaaac[A/G]aacaagaaaaccttc | 2074 |
rs4253175 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480942 | gttccagtagtttcc[A/G]tgtctctagtctcct | 2074 |
rs4253176 | in-del | -/GA | 0.0905309 | 0.192535 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480775 | GCTAGGAATATCACA[-/GA]AGTGATGTGTCTTCC | 2074 |
rs4253177 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480712 | tgtttgttccactat[A/G]ggtgatgttaactct | 2074 |
rs4253178 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480400 | TTTATTCTGTCATGC[C/T]GGTGCTAAAATGATG | 2074 |
rs4253179 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480197 | GATGACTCACCTGGG[A/G]CCTGAAAGGTGAGGA | 2074 |
rs4253180 | snp | C/T | 0.00281312 | 0.0373985 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478310 | TTCCTAAAGCACAAG[C/T]GTGTCTTTCCCTTCA | 2074 |
rs4253181 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477810 | gacacctgagcagag[C/G]cctaaagaaggcgaa | 2074 |
rs4253182 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477718 | TGGGGCCTTCATAGA[C/T]AGCAGGGAGGCCAGT | 2074 |
rs4253183 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477141 | GTTGAGACAGAGTTG[C/T]GGGTGGCTTGGGTGG | 2074 |
rs4253184 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477131 | AGTTGCGGGTGGCTT[A/G]GGTGGTGAGGAGCAT | 2074 |
rs4253185 | snp | A/G | 0.00347825 | 0.0415575 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476810 | GAGAGGTGAAGGGTC[A/G]CAGAGCACGATCGCA | 2074 |
rs4253186 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476797 | TCACAGAGCACGATC[G/T]CATGGAGTGGTTGGT | 2074 |
rs4253187 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476628 | GGGTCATGGGAGGTG[A/G]GATGGTTTGAGCACT | 2074 |
rs4253188 | snp | C/G/T | 0.0107246 | 0.0724382 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476563 | GGCACTGAACTTGCC[C/G/T]GTGAGCAGGAAGCCA | 2074 |
rs4253189 | snp | C/T | 0.00349039 | 0.0416295 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476511 | GGCCCTGGAGGTAGA[C/T]AAGTGACAGAGATGG | 2074 |
rs4253190 | snp | A/G | 0.370162 | 0.219229 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475212 | TTTTGTTCTGTCTTC[A/G]AAATTGGGTATGTAT | 2074 |
rs4253191 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475044 | TACCAATGTTCCTGA[C/G]TTATTCAGATCATTT | 2074 |
rs4253192 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475035 | TCCTGACTTATTCAG[A/T]TCATTTATTGTTAAT | 2074 |
rs4253193 | snp | C/T | 0.295343 | 0.245854 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474751 | TCATGCAGTTTTTTT[C/T]CTGATATAATAATAA | 2074 |
rs4253194 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474745 | AGTTTTTTTTCTGAT[A/G]TAATAATAATCTAAA | 2074 |
rs4253195 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473867 | TTTAGATCTTTCTCT[A/G]GAGTTGGTGTCTAAA | 2074 |
rs4253196 | snp | A/C/G | 3.29641e-05 | 0.00405968 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473613 | TGTATTTGCTTTGCA[A/C/G]ACTCCTATCCCCCAC | 2074 |
rs4253197 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | ERCC6 | GRCh38.p7 | 10:49473111 | AGCCCAGTAATTCCA[C/T]GTGTACAATATGTGG | 2074 |
rs4253200 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472799 | CAGCATACGTTTCAC[A/G]TTTTGATTGTCTCCT | 2074 |
rs4253201 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472531 | CTAGCTTTGTTTCTT[A/G]TAGTCAGTGCTTGTC | 2074 |
rs4253202 | snp | A/C/G | 3.30764e-05 | 0.00406659 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472499 | TTGGGAAGGATTCTC[A/C/G]TTGAGAGGTCTCTCT | 2074 |
rs4253203 | snp | G/T | 0.00335007 | 0.0407899 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472039 | AAAAATGACAAGGTT[G/T]AATGTTACCATATTG | 2074 |
rs4253204 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471641 | CTGGGAGAATAAATG[A/G]CAGGGAGGGACAGGG | 2074 |
rs4253205 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471350 | TTGAAAAAGCTCATT[C/T]GGTGTAAATAATAAG | 2074 |
rs4253206 | snp | A/G | 4.94344e-05 | 0.00497139 | missense | ERCC6 | GRCh38.p7 | 10:49471040 | AATCCAATGATCTCT[A/G]TGAGCTATTTACTCT | 2074 |
rs4253207 | snp | C/T | 0.0067336 | 0.0576321 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470783 | GAAGTTCCCTGCTTC[C/T]AACATATCTGTAAAT | 2074 |
rs4253208 | snp | C/G/T | 0.00761637 | 0.0612425 | ERCC6 | 10 | allele_origin=G(germline)/C(germline) | 10:49470676 | CTTTGAAAGATGACC[C/G/T]TCACATGAGTAGTAA | 2074 |
rs4253209 | snp | C/T | 0.00350262 | 0.0417018 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470615 | GACAAATGCAGTATC[C/T]GGACCAGAAGAGTTG | 2074 |
rs4253210 | snp | C/T | 0.000131898 | 0.00811982 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470426 | AATGGAAAATAATTT[C/T]TATAAGCACAAGTCA | 2074 |
rs4253211 | snp | C/G | 0.135646 | 0.222328 | ERCC6 | 10 | allele_origin=G(germline)/C(germline) | 10:49470271 | TGGTGAAGAAAAGGC[C/G]TTACCAGAAGCAAGA | 2074 |
rs4253212 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470166 | GTAATCCATTTGATA[C/T]GTTTGCCACAGGGAT | 2074 |
rs4253213 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463399 | CTAGAGTGCTCTGCT[A/G]TGTTGAcccaaaacc | 2074 |
rs4253214 | in-del | -/GT | 0.0252325 | 0.109451 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463174 | atatatacattttgt[-/GT]ttagacttggggccc | 2074 |
rs4253215 | snp | C/G | 0.283421 | 0.247756 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463165 | TTTGTGTTTAGACTT[C/G]GGGCCCATCCCCAAG | 2074 |
rs4253216 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462837 | GAGCAGTtgttgccc[A/G]gaggcttgtcaagag | 2074 |
rs4253217 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462544 | agtatttcctcATTG[A/G]TTGTCCTTTATTATG | 2074 |
rs4253219 | snp | G/T | 0.00718218 | 0.0594938 | missense | ERCC6 | GRCh38.p7 | 10:49461370 | ACAGGGGGATTTCTG[G/T]TGCACCAGCAGGAAA | 2074 |
rs4253220 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461263 | TGGAGGCTTATACTG[C/T]TATTTCTCTTCAGGA | 2074 |
rs4253221 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461178 | CTGTTATAACTTTGC[C/T]TTCCTCCTTGCTTTC | 2074 |
rs4253222 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460984 | AGAATGATTTTCCTA[C/G]TTGGAATTGAGAATG | 2074 |
rs4253223 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460646 | GGCATGAGCCACTGC[A/G]CCCAGCCAGCAGTTA | 2074 |
rs4253224 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459623 | CCTTATCCACAGTGT[A/T]CAGGGTCCATTTGAG | 2074 |
rs4253225 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459508 | CTCCACTCTGCCTTC[C/T]TGTCCACCACCATGT | 2074 |
rs4253226 | snp | A/G | 0.35207 | 0.228214 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459399 | GGATTTAGATACCAG[A/G]CCCTCCTCCTTTCCC | 2074 |
rs4253227 | snp | A/G | 0.00233764 | 0.034108 | missense | ERCC6 | GRCh38.p7 | 10:49459183 | CCTGAGCATTTTAGT[A/G]GAAGAGCAGAAGATG | 2074 |
rs4253228 | snp | A/G | 0.000313043 | 0.0125069 | missense | ERCC6 | GRCh38.p7 | 10:49459153 | GCAGACTCTTCATCC[A/G]GGCCCCTCGCTTCCT | 2074 |
rs4253229 | snp | A/G | 0.000148259 | 0.00860858 | missense | ERCC6 | GRCh38.p7 | 10:49459069 | TTAGAAAGTGAAAGC[A/G]GGCACCTGCRGGAAG | 2074 |
rs4253230 | snp | C/T | 0.0134984 | 0.081037 | missense | ERCC6 | GRCh38.p7 | 10:49458975 | CTTTCCAGGCCCACA[C/T]TGATGGCCAGGCCAG | 2074 |
rs4253231 | snp | C/T | 0.241914 | 0.249869 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458762 | AACGGGCATTTCTGA[C/T]TATTAATTTATTATT | 2074 |
rs4253232 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458729 | taatCATGTTTGTCA[A/G]TGGAAGTTGGCTGCA | 2074 |
rs4253233 | snp | A/C | 0.0119091 | 0.0762411 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458697 | TTGATGTTTGTTTGC[A/C]TGATGTCTACCTCAG | 2074 |
rs4253234 | snp | C/G | 0.383053 | 0.211653 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458436 | TATTGGTGCTAAAAA[C/G]AGGTCTTACATTCAG | 2074 |
rs4838518 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461840 | AAAAGACCAAACACT[C/T]AGGAATAAACCCAAG | 2074 |
rs4838519 | snp | A/C | 0.483563 | 0.0891524 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462211 | AGAAAATAGAAATAG[A/C]TTGAACTGCATTTGG | 2074 |
rs4838520 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463870 | cacagccacacagaa[C/T]tgtaagttgattaaa | 2074 |
rs4838522 | snp | C/T | 0.285152 | 0.247516 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475392 | AAGTGTAGTTTGCAT[C/T]CCCTTTCCTGGATAG | 2074 |
rs4838523 | snp | A/G | 0.216048 | 0.247684 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495015 | CAAATATCCTGATAC[A/G]TCCTACACTGTATTC | 2074 |
rs4838524 | snp | C/T | 0.179425 | 0.239831 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502077 | TTTGCTGTCCAAATA[C/T]TTACTATCTGGTACC | 2074 |
rs4838527 | snp | A/G | 0.240478 | 0.249819 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534605 | GGAAGAGAAAGCACA[A/G]GGAAAAATAAGGGGG | 2074 |
rs6537538 | snp | C/T | 0.215446 | 0.2476 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497558 | TCTGCCATTTTCCCC[C/T]TTAGTAGAAAAAATT | 2074 |
rs7072383 | snp | A/C | 0.199254 | 0.244796 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490651 | AGCCACCACGCCCGG[A/C]CAATTTTCAAAATTT | 2074 |
rs7073830 | snp | A/G | 0.29789 | 0.24537 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495184 | CCTTCAGTCTTGCTG[A/G]GAGTTGGGTGCCAGT | 2074 |
rs7075294 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475927 | CACCTACCAGGTAAG[A/G]CCCTCGGAAGTAACA | 2074 |
rs7076173 | snp | C/T | 0.146985 | 0.227789 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485304 | GAGTCAGAATTCGAA[C/T]GGAGAAAGGCAGCCA | 2074 |
rs7079872 | snp | A/C | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485498 | CTGTTAAGAGGGGAT[A/C]TAAAATATTAAAAGG | 2074 |
rs7082895 | snp | A/G | 0.485866 | 0.0828688 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526816 | GGCTGGTGTCCAGAC[A/G]GAGAGATATAATAGG | 2074 |
rs7086144 | snp | C/T | 0.299411 | 0.245069 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465337 | tgcctgtaaccctat[C/T]gtatctaggaagtaa | 2074 |
rs7087700 | snp | A/G | 0.487049 | 0.0794222 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490500 | GCTAGGACTATAGGC[A/G]TGTGCCACCACAACC | 2074 |
rs7092520 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511984 | GACTAAATGAAATTA[C/T]GTATGTACATTATAC | 2074 |
rs7095765 | snp | A/T | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494999 | TTCACTTAGGTGCAG[A/T]CAAATATCCTGATAC | 2074 |
rs7096755 | snp | A/C | 0.488905 | 0.0736498 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527589 | CTGAGGCAGGAGAAT[A/C]GCTTGAACCCGGGAG | 2074 |
rs7342125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492527 | AAAGGAAGAATACAA[C/T]GTATCTATGCTACCC | 2074 |
rs7897502 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530200 | AAACTAAGGAAGTGC[A/G]CCCAAGTGAGGCAAG | 2074 |
rs7903788 | snp | C/G | 0.142272 | 0.225598 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525933 | tccaccttccttcac[C/G]caacattatgctttt | 2074 |
rs7903930 | snp | C/G | 0.214843 | 0.247516 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495951 | TGCCCACTGCTCTTG[C/G]GACAGAGATTAAACA | 2074 |
rs7909342 | snp | C/T | 0.284733 | 0.247575 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479675 | ATAAAGAAAACTGCC[C/T]CCACATCCTCCCTCC | 2074 |
rs7920256 | snp | A/G | 0.298144 | 0.245321 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496100 | TCTTCCCTTCCTCCA[A/G]TCGACCTTCACCATG | 2074 |
rs7922756 | snp | G/T | 0.483708 | 0.088773 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495549 | CCCAGATCACTCTTC[G/T]GAACTCCAAACCACC | 2074 |
rs7923460 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526117 | tatatttatatattt[A/T]tatatatatatatat | 2074 |
rs7923762 | snp | C/T | 0.214843 | 0.247516 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526379 | aatttatcttttgga[C/T]agccttttttgtgta | 2074 |
rs10437449 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472639 | TGAACAGCCAGTTGA[A/C]AAGACATCTCTACTT | 2074 |
rs10776575 | snp | C/T | 0.379746 | 0.213696 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454376 | GGGAGCTGAGGGAGA[C/T]GGAGCTCTGTTTTCT | 2074 |
rs10776576 | snp | A/G | 0.352938 | 0.227824 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495587 | AGAAATCTCACTGCC[A/G]ATATCCCCAAAGCAC | 2074 |
rs10776577 | snp | C/T | 0.124837 | 0.216412 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534307 | TAGTAAAGCCCCTTG[C/T]AGGGACAACTTAGCA | 2074 |
rs10857497 | snp | A/G | 0.370162 | 0.219229 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484300 | aaaaaaagaaaaaaa[A/G]aaaaagaaAATGTTA | 2074 |
rs10857498 | snp | G/T | 0.289683 | 0.24683 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490032 | AGAAAAAAGGATCAC[G/T]AAATATAATCAGAAA | 2074 |
rs10857499 | snp | A/G | 0.208169 | 0.246476 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496991 | CCCTTATACTCCAAC[A/G]TAACAAAATAACCTA | 2074 |
rs10857500 | snp | A/T | 0.290201 | 0.246747 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517794 | AGCAATCCTCCTGCC[A/T]TGGCCTCCTAAAGTG | 2074 |
rs10857501 | snp | A/G | 0.244898 | 0.249948 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534165 | AAAAACAAAAAAAAA[A/G]CTCCATTTTAATACA | 2074 |
rs10857502 | snp | A/G | 0.199254 | 0.244796 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534407 | ACACACAGGTGCAAG[A/G]ATGTTTAGTGCAGCA | 2074 |
rs11101137 | snp | A/G | 0.290201 | 0.246747 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456985 | GTATTTGCTACTTGA[A/G]GAGGAGGCTATACCT | 2074 |
rs11101138 | snp | C/T | 0 | 0 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458487 | TGTTCTGCAAACTTC[C/T]AACTGTGCTCCCTGA | 2074 |
rs11101139 | snp | A/G | 0.102513 | 0.20186 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478508 | AACATTACTATATAT[A/G]TTTAAGGAACGCATT | 2074 |
rs11101140 | snp | A/G | 0.370974 | 0.218781 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484728 | CTAGACAACGGCGCA[A/G]GATCCTGACTCAAAA | 2074 |
rs11101141 | snp | A/T | 0.29789 | 0.24537 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488659 | TTTTTTTTTTTTTTT[A/T]AAGTTTTTTACTCCC | 2074 |
rs11101142 | snp | A/G | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499455 | CGCTGCTGATGAGCT[A/G]GAGAGTAGGAAGAAC | 2074 |
rs11101143 | snp | C/G | 0.0025192 | 0.0354013 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515779 | TTGGCTGCTGAACTT[C/G]TATCTTCTTTTTCAG | 2074 |
rs11101144 | snp | A/T | 0.392696 | 0.205275 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517296 | TTCTTAAAAATTACT[A/T]GTATAGGATGTAGTG | 2074 |
rs11101145 | snp | C/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517627 | AACACAGTCTTCTTT[C/T]TTTTTTTTTTTTCTC | 2074 |
rs11101146 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522670 | GACCCAATTTAATTG[A/G]AAAAATATATATTGC | 2074 |
rs11101147 | snp | C/T | 0.214843 | 0.247516 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522983 | TTGACACATCTATTT[C/T]GGAAAGGTTATGGAA | 2074 |
rs11101148 | snp | C/T | 0.485933 | 0.0826777 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525857 | GACCTGGACTCCTAA[C/T]GTACAGACAAGTTGT | 2074 |
rs11101149 | snp | A/T | 0.291493 | 0.246533 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526099 | TTTATATTTATATAT[A/T]TATATATTTATATAT | 2074 |
rs11101150 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526107 | TATATATTTATATAT[A/T]TATATATTTTTATAT | 2074 |
rs11101151 | snp | A/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526115 | TATATATTTATATAT[A/T]TTTATATATATATAT | 2074 |
rs11101152 | snp | A/C | 0.229136 | 0.249128 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540515 | CAGCTATTTTGGAGA[A/C]CCTTCCTATATCAGA | 2074 |
rs11302216 | in-del | -/C | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538890 | GGCGCGGGGCCGCGG[-/C]CCGCCCGAGAAGCCT | 2074 |
rs11400742 | in-del | -/T | 0.364817 | 0.222075 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490357 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 2074 |
rs11424862 | in-del | -/T/TTT | 0.487241 | 0.0788465 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482557 | TTTTTTTTTTTTTTT[-/T/TTT]AACCAGATACCAATT | 2074 |
rs11592167 | snp | C/G | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477544 | ATCACTCATGACTTC[C/G]TAGTGGCCAAACACA | 2074 |
rs11817117 | snp | C/T | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525584 | AAAATACCAAAAGAC[C/T]TAAGGCTTAATAGGA | 2074 |
rs12217467 | snp | A/C | 0.370772 | 0.218893 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467039 | acccacctcggcctc[A/C]caaagtgctgggatt | 2074 |
rs12220085 | snp | C/T | 0.289942 | 0.246789 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522134 | ATGTTGTAAACTCTA[C/T]GACTTTATTCTAATC | 2074 |
rs12220258 | snp | C/T | 0.417683 | 0.185425 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461774 | CTTCCTATTTACAAA[C/T]AATAGCCAGCTAAAA | 2074 |
rs12220937 | snp | A/G | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481569 | GACCTGGTAGGCACA[A/G]GCCCACCCAAGAAGG | 2074 |
rs12221460 | snp | A/C | 0.290201 | 0.246747 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461748 | AAAATTCACACACAG[A/C]AACCTATAACCTTCC | 2074 |
rs12242851 | snp | C/T | 0.27008 | 0.249192 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538255 | ACACAGGCACAGTTC[C/T]GAGAGGGGACAGGCA | 2074 |
rs12252365 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510342 | CAGCTAGCTACCACC[A/G]TGCCATACCATGTAT | 2074 |
rs12257890 | snp | C/G | 0.00271246 | 0.036727 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488198 | AGATGTCTGTGAAAG[C/G]GCTGCTGTTATTATG | 2074 |
rs12265674 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460227 | TTCAAGTGAATGTGC[A/G]TCGTAAATCAGAGCG | 2074 |
rs12355956 | snp | C/G | 0 | 0 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456858 | GGTAACAATGTGTCA[C/G]ATCTCCACACTGAGA | 2074 |
rs12411454 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49507797 | tgctaaacatcctac[A/C]ccacacaggacagcc | 2074 |
rs12412526 | snp | A/G | 0.216048 | 0.247684 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496637 | ACATGGTGAAACCCC[A/G]TCTCTACCTAAACTA | 2074 |
rs12571445 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514137 | AATGTTGTCTTAAAA[A/G]AACATCAGGACTAAG | 2074 |
rs12572909 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493372 | AAACAATGCTAACTA[C/T]GGAAATTTATTGATA | 2074 |
rs12770711 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517763 | tgcccaggctggtct[C/T]gaactcttgagctca | 2074 |
rs17010102 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462297 | AAATGATGCTACAAA[C/T]GTTGGGGCACAAACG | 2074 |
rs17010116 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490022 | GCTCTATATTAGAAA[A/C]AAGGATCACGAAATA | 2074 |
rs17010145 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521815 | GCAGGATCCAAAGGG[C/T]GACTGCCCAGTTCCA | 2074 |
rs17177355 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475856 | ATCCTCTCCACAAGA[C/T]ATATAATTCTGGTCA | 2074 |
rs17177522 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511048 | GAAGGAAAGCTCATC[A/G]TTTTGAACAATAAAA | 2074 |
rs17775180 | snp | A/C | 0.297128 | 0.245518 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490271 | GAGAGAGGTGGGAAG[A/C]TAAAGGGCAACTTGG | 2074 |
rs17775216 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502870 | AGGTCGAGAAACCCT[C/G]ATTTAGAACAAAAGC | 2074 |
rs28454254 | snp | A/G | 0.290201 | 0.246747 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467552 | ATTATTTGTCCATTT[A/G]AAAAATTGGGTTATA | 2074 |
rs28506155 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526640 | AGCCTTAGGTCTTTA[C/T]ACTGAGTATTTTGCT | 2074 |
rs34252261 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49504639 | TGTTTCTTAACAAAG[-/A]ATCACTGTAGAGAAA | 2074 |
rs34398498 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49490642 | CAGGCATGAGCCACC[-/C]ACGCCCGGCCAATTT | 2074 |
rs34399938 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49471273 | GAAAATTACAATTCA[A/G]GAAATATATAATACA | 2074 |
rs34436591 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49468871 | GTGCTCAAAGAATGG[-/T]TGGGGACATACCAGA | 2074 |
rs34455522 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49461170 | AGGGGATGAAAGCAA[-/G]GGAGGAAGGCAAAGT | 2074 |
rs34575215 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49530449 | TACGATGGGTTTGTC[-/G]GGGATGTAACCCTGT | 2074 |
rs34608002 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49538329 | CACTCCCAGTGCAAT[-/G]GGAATGACTCTGAAA | 2074 |
rs34614020 | snp | A/G/T | | | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540113 | GCACGATGTGGGCTC[A/G/T]CTGCAACCTCCTCCT | 2074 |
rs34704611 | snp | C/T | 0.00512674 | 0.0503695 | missense | ERCC6 | GRCh38.p7 | 10:49470301 | CCAAGTTTGAAGGAA[C/T]TCGAATTCCACACCT | 2074 |
rs34761792 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503168 | AACTTAACTAAAGTA[-/G]GGGAGAGTGCGGAAA | 2074 |
rs34811588 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49535301 | CAAATCTGAGCTCAA[-/G]GGGAAAGTCTGGGTG | 2074 |
rs34917815 | snp | G/T | 0.00140697 | 0.0264859 | missense | ERCC6 | GRCh38.p7 | 10:49459232 | CTTCTTTTTATAGGA[G/T]GGCATCATGAAAAAG | 2074 |
rs34950053 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488866 | TCAGCTCACTGCAAG[-/T]TCCGCCTCCCAGGTT | 2074 |
rs34958861 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49465596 | CCTCCCACAACACAT[-/G]GGGAATTGTGGGAGT | 2074 |
rs35050163 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513839 | ATATCAATACTATTG[G/T]TATTCTCTCTCTCTC | 2074 |
rs35149063 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49529881 | TGTACATAAATCCTT[-/A]AAAAAAGTTTCAAAC | 2074 |
rs35170115 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527872 | CACACATACACACAC[A/G]CAATGACTGCAAAGA | 2074 |
rs35170156 | in-del | -/T | | | utr-variant-5-prime, intron-variant | ERCC6 | GRCh38.p7 | 10:49539088 | GCCCCCAACAGCGAC[-/T]TCCGACTTCTGCTGG | 2074 |
rs35182583 | snp | A/G | 0.00517752 | 0.0506158 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482774 | TGACTTCATCTTCCC[A/G]GGAAAGTTAGGCACG | 2074 |
rs35305152 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49513717 | TCGTGAGAACAGCAT[-/G]GGGGGAAACCGCCCC | 2074 |
rs35323997 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49462911 | ATTATTCAAACAAAC[-/G]AAACAAAACAAACTT | 2074 |
rs35337487 | in-del | -/T | | | intron-variant, frameshift-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49515383 | TAAGGCAACATCACA[-/T]TTTTTCACATCGAAA | 2074 |
rs35365613 | snp | C/T | 0.00227145 | 0.0336239 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470774 | TGCTTCTAACATATC[C/T]GTAAATGATGCCACA | 2074 |
rs35407743 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49477640 | TGTCTGTGCCAGCCT[-/C]CCCCAGTCTTCCCAG | 2074 |
rs35442898 | in-del | -/CA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495556 | ACTCTTCGGAACTCC[-/CA]AAACCACCACACACT | 2074 |
rs35471849 | snp | G/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456135 | ATTGCTATAATAGAC[G/T]TCAAAAGACAGTAGC | 2074 |
rs35585732 | in-del | -/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534607 | AGAGAAAGCACAGGG[-/G]AAAAATAAGGGGGAA | 2074 |
rs35619111 | in-del | -/A | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49472104 | AGAAATATTCCTTTC[-/A]AAATAACAATATGAA | 2074 |
rs35756610 | snp | A/G/T | 0.00522554 | 0.0508494 | synonymous-codon, missense | ERCC6 | GRCh38.p7 | 10:49470186 | AAAGCTTTTCAAAAA[A/G/T]TCAGGTAATCCATTT | 2074 |
rs35782652 | in-del | -/C | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523218 | TTCCTTAGAGCTAAG[-/C]TGAGCTCTAAGTCAA | 2074 |
rs35884044 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49503460 | CCCCAAAAACTAGGG[-/C]ATAGTTACAAAGATA | 2074 |
rs35907997 | snp | A/G | 0.100231 | 0.200173 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527572 | TCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 2074 |
rs35909102 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470112 | CTGTTTCTAGCAGTA[A/G]CAGTCTTTAACTGAT | 2074 |
rs36024883 | in-del | -/A | | | frameshift-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524685 | AGGGATCTGGGTACC[-/A]AAAAGGTGTCATCTG | 2074 |
rs36032377 | snp | A/G | 0.000132024 | 0.00812371 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49500648 | ATTGCACTGCCAGCA[A/G]GCAGGAGGAATTCTG | 2074 |
rs36050955 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49484071 | TTGCTTGAGCCCAGG[-/T]AGTTCGAGACCAGCC | 2074 |
rs36057162 | in-del | -/AC/ACAC | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537508 | TATATATATACACAT[-/AC/ACAC]ACACACACACACACA | 2074 |
rs41281953 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456213 | AGAGCAGTTCAAGAC[C/T]GGCAGGCCAACTTCT | 2074 |
rs41281955 | snp | A/G | 0.0133456 | 0.0805897 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516362 | TCTCTCATTAAGTTT[A/G]CTTATGAGAGGTCGC | 2074 |
rs41281957 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | ERCC6 | GRCh38.p7 | 10:49532798 | CACCCCACAGCAGAG[A/G]TGGACAGCCCGTCAC | 2074 |
rs41281959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533194 | ACCAGAAAAAGAAAT[A/G]CAGTATCATCAACAA | 2074 |
rs41309397 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ERCC6 | GRCh38.p7 | 10:49460267 | AATATCAGGTGTCAT[C/T]ACACCAGAGATGACC | 2074 |
rs41547412 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459433 | TTTTTTTTTAGGAAA[C/T]GGTCTCTTAACAGTG | 2074 |
rs41547818 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538925 | CCGAATGTCGGGCAG[G/T]GGGTGTCGGGGCCCA | 2074 |
rs41549213 | snp | A/G | 0.000445093 | 0.0149113 | missense | ERCC6 | GRCh38.p7 | 10:49500553 | GCAAGATCAGGACTC[A/G]TGGTTCAAATTACAG | 2074 |
rs41549314 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461687 | TATTTTTTATCATTG[A/G]TTCTCTAGGGTTTTC | 2074 |
rs41555314 | snp | C/G | | | missense | ERCC6 | GRCh38.p7 | 10:49470731 | AAATCTGAGGCTAAA[C/G]GAGCTGAAGTAAATG | 2074 |
rs41555612 | snp | A/G | | | missense | ERCC6 | GRCh38.p7 | 10:49471089 | TTTTTGACAAATAGA[A/G]TGCTAAAAGACCCAA | 2074 |
rs41557921 | snp | C/G | | | missense | ERCC6 | GRCh38.p7 | 10:49472935 | GTCATCTATGACCCA[C/G]ACTGGAACCCAAGCA | 2074 |
rs41562713 | snp | A/G | 0.00209162 | 0.0322713 | missense | ERCC6 | GRCh38.p7 | 10:49470984 | ACTGAAACAAGTGCA[A/G]TTTTTGCAGGTATTA | 2074 |
rs41563016 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531035 | AGATAAAAGAAAACA[C/T]TAGCAGTCATCTTAA | 2074 |
rs45534740 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528244 | CCTGCAGAACCAAAT[A/C]CCTCTCAAAGAGAAT | 2074 |
rs55698015 | snp | A/G | 0.000955393 | 0.0218354 | missense | ERCC6 | GRCh38.p7 | 10:49482760 | ATAAACACAGGCAAC[A/G]TGCCTAACTTTCCCG | 2074 |
rs55710235 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49474308 | GATTCCCTAGGCAAG[A/G]AGGCTGTTTAACCTA | 2074 |
rs55710382 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49530609 | TCTCTATTGTAATTA[-/T]TAAGTATTTGCTTCA | 2074 |
rs55719105 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482382 | TAACTGCTCTTCTGA[C/T]CACATGTGACATCTT | 2074 |
rs55721411 | snp | C/T | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539372 | ATGCGAATGTAAATC[C/T]TCACAATTAACCTTG | 2074 |
rs55775940 | snp | C/G | | | upstream-variant-2KB, intron-variant | ERCC6 | GRCh38.p7 | 10:49539248 | CTCCGCTGCCGGTCA[C/G]CTGGGTGGCTTGCGA | 2074 |
rs55784032 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528754 | ACAGGCATGCCTGCA[A/C]CCCCATGCTCTCCTG | 2074 |
rs55801003 | in-del | -/ATATATATATATATATATATATATATAT | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526135 | TATATATATATATAT[-/ATATATATATATATATATATATATATAT]CTGGGTATGCTAAGC | 2074 |
rs55828359 | snp | C/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49492932 | TTAGAACAATAAGAC[C/G]TATATTCATAACTGT | 2074 |
rs55838288 | snp | C/T | 1.65252e-05 | 0.00287443 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459220 | ATCTTTTCCCTCCTT[C/T]TTCATGATGCCATCC | 2074 |
rs55881102 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49528389 | CATCAATTCAAGAAC[A/C]CAGAGAAACTGCTCC | 2074 |
rs55968328 | in-del | -/TATTT | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506416 | ACAAAAAATAGATTT[-/TATTT]ATAATTACTATTTCT | 2074 |
rs55975158 | snp | A/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523842 | CTAGAAGTACATGCA[A/T]TTGGGGCCAGCATCA | 2074 |
rs55986153 | in-del | -/CTT | | | cds-indel | ERCC6 | GRCh38.p7 | 10:49476244 | TGAGAATCCTGTAAA[-/CTT]CTTTGGAATCAACGA | 2074 |
rs56023419 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528109 | CATGTAATTTAATCA[C/T]GATGCTAGTTGTCTT | 2074 |
rs56089364 | snp | C/T | 0.000481684 | 0.0155116 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524285 | TCGTCATCTTCCTCC[C/T]CTTCCTCCTCCTCTG | 2074 |
rs56105202 | snp | A/C/G | 0.0130921 | 0.0798413 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492528 | AAGGAAGAATACAAC[A/C/G]TATCTATGCTACCCA | 2074 |
rs56292234 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471266 | AGCCTTGGAAAATTA[C/T]AATTCAGGAAATATA | 2074 |
rs56296961 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524248 | ACCATCTCCAGACAG[A/G]TCCGCCTCTGCCCCC | 2074 |
rs56298337 | snp | A/C | 1.65523e-05 | 0.00287678 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506032 | CATGAAAATAAAAAT[A/C]ACATTTCCATTATTT | 2074 |
rs56318749 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483054 | ATGAAAAAATGAGAA[A/T]GAATTTTTTCTTATT | 2074 |
rs56333631 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49472528 | AATGACAAGCACTGA[C/T]TATAAGAAACAAAGC | 2074 |
rs56345022 | in-del | -/A | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530880 | TTTTGCACTCTGATA[-/A]CATTTTTATAGCATA | 2074 |
rs56397747 | snp | C/T | 4.9629e-05 | 0.00498117 | missense | ERCC6 | GRCh38.p7 | 10:49476297 | TGCTCATCTGTAAGA[C/T]GGCAAAATAAGACCT | 2074 |
rs56799380 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49537895 | GCCCGGCTAATTTTT[C/T]GTATTTAGTAAAGAC | 2074 |
rs56800969 | in-del | -/TTTTAT | | | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526115 | TATATATTTATATAT[-/TTTTAT]ATATATATATATATA | 2074 |
rs57460451 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467283 | ATCACAAGGAAAGCG[C/T]ATGCAACTGCCAAAC | 2074 |
rs57612136 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517938 | AAATCTCAAACTTTT[A/G]CTAAATTCAGATTTT | 2074 |
rs57761316 | snp | A/G | 0.422315 | 0.181128 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49541122 | TCCTCATGGCTTGCA[A/G]ATGGTTACCTTCTCA | 2074 |
rs58002245 | snp | C/T | 0.297128 | 0.245518 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490648 | ATGAGCCACCACGCC[C/T]GGACAATTTTCAAAA | 2074 |
rs58366774 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534432 | GCAGCACATTTTTAA[C/T]AGTTTAATGTAACTA | 2074 |
rs58626977 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49485377 | TACTAAAATATAAAA[A/G]AAAAAGTTTAAAAAG | 2074 |
rs58711755 | snp | C/T | 0.274929 | 0.248754 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526737 | CTAATGAAAGAGGGA[C/T]ACTTTCTGGGTGACT | 2074 |
rs58985498 | snp | A/T | | | missense | ERCC6 | GRCh38.p7 | 10:49460450 | TCTTACCAAATCTAC[A/T]CCTAAAAAAGGAAAA | 2074 |
rs59898389 | snp | C/T | 0.275999 | 0.248644 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521738 | AGAAGGGGGAATACA[C/T]GGTTTGAAAAATGGT | 2074 |
rs60049731 | in-del | -/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534155 | AAAAAAAAAAAAAAA[-/C]AAAAAAAAAACTCCA | 2074 |
rs60598505 | in-del | -/ATATATATACACTTTCCTGATACACATATCTGAATTCTTG | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507962 | ATATCTGAATTCTTG[lengthTooLong]CTACTCACTCTGAAA | 2074 |
rs61217679 | in-del | -/A | 0.148661 | 0.22854 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468984 | GGATTACAGTCATGG[-/A]AAAAAAAAGAATCCA | 2074 |
rs61288726 | snp | C/T | 0.422315 | 0.181128 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540856 | CATCACTTGTGTCCT[C/T]CACTCCCTGGATGCC | 2074 |
rs61329670 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479731 | CGAGCATGCTGGTTG[C/G]AGGTGCTGGTCAACT | 2074 |
rs61352664 | snp | A/C | 0.0543475 | 0.155628 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534164 | AAAAAACAAAAAAAA[A/C]ACTCCATTTTAATAC | 2074 |
rs61545702 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467185 | CTAATAAAGCTGCTA[C/T]GAATATTCATGTACA | 2074 |
rs61749175 | snp | A/G | 0.000396268 | 0.0140704 | missense | ERCC6 | GRCh38.p7 | 10:49505975 | CCTCCAGCTTCAGAC[A/G]TTTCTCTTTGTCCTG | 2074 |
rs61760163 | snp | A/G | 0.00326027 | 0.0402431 | missense | ERCC6 | GRCh38.p7 | 10:49482860 | TCCGATGAGGGGTGC[A/G]AAACTATTTGAGGAA | 2074 |
rs61760166 | snp | A/C | 0.00120187 | 0.0244845 | missense | ERCC6 | GRCh38.p7 | 10:49470310 | ATTCGAGTTCCTTCA[A/C]ACTTGGCGTCTCTGC | 2074 |
rs61760167 | snp | C/G/T | 0.00269818 | 0.0366312 | missense | ERCC6 | GRCh38.p7 | 10:49459074 | TGCAGGTGCCCGCTT[C/G/T]CACTTTCTAAACGCT | 2074 |
rs61846612 | snp | A/G | 0.275732 | 0.248672 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527504 | ACATGGTGAAACCCT[A/G]TTTCTACTAAAAATA | 2074 |
rs61846613 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49527537 | AAAAATTAGCTGGGC[A/G]TGGTGGTATGCGCCT | 2074 |
rs61846614 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49533825 | TAAAGTTTTTTTAAA[A/G]GATTAATTAAAATAT | 2074 |
rs61846615 | snp | A/G | 0.275999 | 0.248644 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534565 | GATCTGGCAGGATAC[A/G]AACTAAGCCTGCAAA | 2074 |
rs61846616 | snp | C/G | 0.185788 | 0.241613 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538159 | TAATCATCTGGGACA[C/G]TAGTATCTTCACCGT | 2074 |
rs61846617 | snp | A/G | 0.271972 | 0.249033 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540228 | GTTTTTAGTAGAGAC[A/G]GGGTTTCGTCATGTT | 2074 |
rs61846618 | snp | C/T | 0.225301 | 0.248777 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49541047 | TTGTTTCTCATAGTT[C/T]TGGAGGCTGGGAAGT | 2074 |
rs61851012 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488049 | ACGGCTCTATCCAAA[C/T]ACTTAAGACAAATCA | 2074 |
rs61851014 | snp | A/C/T | 0.00319074 | 0.0398324 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493886 | GGAGGAGCATCCGAG[A/C/T]GAGTGTTCTCTCCTG | 2074 |
rs61851015 | snp | A/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520034 | AAGGCTCCCTGCCAG[A/G]CCCTCCCCTGTGTAC | 2074 |
rs66834567 | in-del | -/T | 0.24134 | 0.24985 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511428 | CATCTTCTTTTTTAC[-/T]TTTTTTTTTTTTTTG | 2074 |
rs71026250 | in-del | -/A | 0.484841 | 0.0857308 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454136 | CCAAAGAACAGAGAG[-/A]AAAAAAAATGAAAAA | 2074 |
rs71026253 | in-del | -/ATATATATATATATATATATATATATAA | 0 | 0 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526117 | TATATATATATATAT[-/ATATATATATATATATATATATATATAA]AAATATATAAATATA | 2074 |
rs71026254 | in-del | -/G/T | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534154 | GGAGCTTTTTTTTTG[-/G/T]TTTTTTTTTTTTTTT | 2074 |
rs71026255 | in-del | -/TG | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537535 | CACCACAATTATATT[-/TG]TGTGTGTGTGTGTGT | 2074 |
rs71500276 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537971 | GGGTGATCCACCCAC[C/T]TCGGCCTCCCAACAA | 2074 |
rs72209777 | in-del | -/ATTTT | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506413 | GTAACAAAAAATAGA[-/ATTTT]TTTATAATTACTATT | 2074 |
rs72792889 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462728 | TGGTCCTATAAAAAG[C/T]TCAATTTCACTCAAA | 2074 |
rs72792894 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494841 | TGATTACAAGGACAC[C/T]TGGCCTTAGGCAAAA | 2074 |
rs72792895 | snp | C/G | 0.067446 | 0.170804 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496045 | ACTGCCATTATCCTA[C/G]CACTTGCTCCTGTGG | 2074 |
rs72793793 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502355 | CTAAAAATCAAAACA[C/T]GATGAAGTGTAGTAC | 2074 |
rs72793796 | snp | C/T | 0.00881725 | 0.0658094 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528374 | ACTACAGGCATCAGG[C/T]ATCAATTCAAGAACA | 2074 |
rs72793798 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534846 | ACTCATCCCTTATTA[A/G]GTAAAATAAGCCCAG | 2074 |
rs73297746 | snp | C/T | 0.078151 | 0.181571 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454053 | TTCCTTTTTCTTCTG[C/T]TCTTCTTGTACTCCC | 2074 |
rs73297748 | snp | A/G | 0.290201 | 0.246747 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454992 | TGGGATTAATAATTC[A/G]TAAGAATGTATTCAT | 2074 |
rs73305562 | snp | C/T | 0.290201 | 0.246747 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468119 | CATGTTTCCTCTAAT[C/T]CGAAAAGTTAAAGAG | 2074 |
rs73305563 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469905 | TAACTGCCTACTAAT[A/G]TTCAGGTAGTACACA | 2074 |
rs73305568 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481109 | AGGGGCATCAGATCT[A/G]CAACCTGCCCTCAGG | 2074 |
rs73305578 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485535 | TTTTTAAATGTTACT[A/G]TAATTCCTGTTCAGT | 2074 |
rs73305599 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502145 | AGCTCATTTAACTGG[C/T]TTTATTTAATCTCCT | 2074 |
rs73311017 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527094 | AGTGTCAGCTGCTGT[A/G]GACAGGCAGAGTGGA | 2074 |
rs73311019 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527118 | GAGTGGAACAAGGAT[A/G]AAAAGGGGCTCTTGG | 2074 |
rs73311033 | snp | G/T | 0.0955749 | 0.196603 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540723 | CACCCCGGGACCTCA[G/T]AATGTGACTGTATTT | 2074 |
rs74130975 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502597 | GCCAAAGGTGACATC[A/G]CTAGAAAAAAATGAG | 2074 |
rs74338098 | snp | C/G | 0.0217236 | 0.101931 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454338 | ATCTTGCCCCTCCCT[C/G]TGAGGTACCATACCT | 2074 |
rs74397002 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484724 | CAGGCTAGACAACGG[C/T]GCAAGATCCTGACTC | 2074 |
rs74506984 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509225 | TCACATATAAAGCAC[C/T]TTAGCACAGAACCTA | 2074 |
rs74561842 | in-del | -/AA | | | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458594 | TGCCAAAAAAAAAAA[-/AA]TCAATCCAAGTATTT | 2074 |
rs74579386 | snp | G/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490373 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCGCT | 2074 |
rs74693932 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524598 | AAGACAGTTTTGCTT[C/G]ATCTGCCAAATACTT | 2074 |
rs74700584 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462312 | CGTTGGGGCACAAAC[A/G]TTGGGGCATTTTATC | 2074 |
rs74733025 | snp | A/G | 0.000132159 | 0.00812787 | missense | ERCC6 | GRCh38.p7 | 10:49473024 | AACACAAATATGGAT[A/G]TGTCCTAGAGGTAAG | 2074 |
rs74750824 | snp | A/G | 0.00259981 | 0.0359603 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475446 | GAAAGACCTGAAGAA[A/G]TTAAGGGGAGATTCA | 2074 |
rs74797785 | snp | A/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501812 | AAAAAAAAAAAAATT[A/T]AGCCAGGAGTGGTGG | 2074 |
rs74800786 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526886 | AGATCTGTATAAGGT[A/G]CTAGTAGAACCTAGG | 2074 |
rs74840240 | snp | C/G | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463727 | CTCATGAGACTCATT[C/G]ACTATCGTGAGAACA | 2074 |
rs74902207 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49467046 | TCGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 2074 |
rs74944791 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461846 | CCAAACACTTAGGAA[A/T]AAACCCAAGCAATGT | 2074 |
rs75026490 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534961 | CAGAGCAGGGCAGGT[C/G]AGCTAGCCCGGGACA | 2074 |
rs75070303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509902 | GCAGCCACATAAAAC[A/G]AAGTGGTGGGCATGG | 2074 |
rs75139617 | snp | C/T | 0.0383715 | 0.133092 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454490 | ATTTTCTTGAATAAG[C/T]GTTACTTTATTCTAC | 2074 |
rs75166536 | snp | C/G/T | 1.64802e-05 | 0.00287051 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482759 | CATAAACACAGGCAA[C/G/T]GTGCCTAACTTTCCC | 2074 |
rs75226363 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466054 | ATAACATAGAGTCAA[C/G]AAGGATGGGAGGAAA | 2074 |
rs75319648 | in-del | -/TA | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49473832 | GAATCACATGGTGAG[-/TA]CTTTTTTAAAAAGTC | 2074 |
rs75344111 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528034 | AAGCCTGCCAAATAC[A/G]CTCTTTAAAGACACG | 2074 |
rs75448943 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535314 | CAAGGGAAAGTCTGG[A/G]TGACATGTGGACACA | 2074 |
rs75692647 | snp | G/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511439 | TTACTTTTTTTTTTT[G/T]TTTGAGACAAAGTCT | 2074 |
rs75941022 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520258 | CACTTCCTAAGTCAG[A/C]GTCTCCAGTGTTAGG | 2074 |
rs76060723 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534417 | GCAAGAATGTTTAGT[G/T]CAGCACATTTTTAAT | 2074 |
rs76062895 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522312 | TCCTGAGCATTTTAT[C/T]TTCTTTCATCCCCCA | 2074 |
rs76742279 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506411 | TATGTAACAAAAAAT[A/T]GATTTATAATTACTA | 2074 |
rs76754845 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502118 | TCTACCTAAAATCTC[A/T]TTTTGGACTTCAGCT | 2074 |
rs76920898 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469705 | GCAGGGCTATCTATA[C/T]ACTCCATGGTCTTGA | 2074 |
rs76925204 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535187 | TCACCAGTGAATTCA[A/G]TCACAAAAATGAGAC | 2074 |
rs76967670 | snp | C/T | 0.100588 | 0.200439 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533645 | TGTCTCTACTAAAAA[C/T]TTAAAACCTTAGCCA | 2074 |
rs76977396 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525332 | GTTAAAAACTCAGTT[C/T]CACAGTTGCATTTGC | 2074 |
rs77027474 | snp | C/T | 0.000214187 | 0.0103464 | missense | ERCC6 | GRCh38.p7 | 10:49474115 | ATCATTTTCCCAGAA[C/T]GTTTCCAGTACCCAA | 2074 |
rs77030623 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508146 | ATAAACCTTGGAAGA[A/C]TCACAGCCACTTAAA | 2074 |
rs77066892 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521518 | AAGCAAATGGAAACC[A/G]TGGTAGCACAAAGTA | 2074 |
rs77077380 | snp | A/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509226 | CACATATAAAGCACC[A/T]TAGCACAGAACCTAG | 2074 |
rs77093089 | snp | A/G | 0.109461 | 0.206758 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540865 | TGTCCTTCACTCCCT[A/G]GATGCCTATGCTCAG | 2074 |
rs77157840 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49475408 | CCCTTTCCTGGATAG[G/T]GTGATCTAGACCCCC | 2074 |
rs77184432 | snp | C/T | 0.0349115 | 0.127424 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525958 | GCTTTTGAGCTGCAT[C/T]CTTACTGTTGAATGT | 2074 |
rs77275715 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469440 | AGCTGAAAAATGTTA[A/G]TAACTTAGATAAAGG | 2074 |
rs77416597 | in-del | -/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49526317 | GTACCACATTATGGC[-/T]TATAATTTACATTTC | 2074 |
rs77451159 | snp | C/T | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488644 | ATGTGGCCTCTTTCT[C/T]TTTTTTTTTTTTTTA | 2074 |
rs77588659 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499696 | TTACCAATACTGATT[C/T]CTACAGAGTCAATTT | 2074 |
rs77668127 | snp | A/G | 0.375 | 0.216506 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484292 | TCAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAGA | 2074 |
rs77729515 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | ERCC6 | GRCh38.p7 | 10:49469068 | ACCTTCCTTACAATA[A/G]AATGTTAATCACCAT | 2074 |
rs77824193 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538178 | TATCTTCACCGTCCT[A/C]CCCCATCACTGGGGC | 2074 |
rs78104810 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486809 | TAGGACTAGATCCTA[C/T]TACTGAAATTGTTCC | 2074 |
rs78149856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464093 | AATGTGGGAAGGTTT[A/G]CAACTTCCTAGAGAC | 2074 |
rs78370243 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455868 | AACAAAACAACCTAT[C/T]GATATTGATACCACT | 2074 |
rs78645997 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458451 | GTTTTTAGCACCAAT[A/T]AAAAAAAATATTGAG | 2074 |
rs78727017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489508 | CAGCAGATCCAAGAT[C/T]CGAACCCTGGTCTTG | 2074 |
rs78757296 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518088 | GGGTGCAAACCAGGA[G/T]CCAACTGAAGGACAG | 2074 |
rs78952611 | snp | A/C/T | 0.0383715 | 0.133092 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463865 | GCCTCCACAGCCACA[A/C/T]AGAACTGTAAGTTGA | 2074 |
rs78989372 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526222 | GTTACGTTCCAAAGT[C/T]CCCATCAACTGTGTC | 2074 |
rs79042401 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517638 | CTTTCTTTTTTTTTT[C/T]TCTCTCAGGCTCCAG | 2074 |
rs79068233 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526630 | GCCTCAATTAAGCCT[A/T]AGGTCTTTACACTGA | 2074 |
rs79131660 | snp | G/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49506412 | ATGTAACAAAAAATA[G/T]ATTTATAATTACTAT | 2074 |
rs79193479 | snp | G/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537732 | AATTTTTTTTTTTTT[G/T]GAGACGGAATTTCGC | 2074 |
rs79248189 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489849 | CCTTCTTTATCTCTT[C/T]ATTTACTACATTTTC | 2074 |
rs79324668 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468701 | ACTATTGGCTACGAA[A/C]GCAATGACATAATAG | 2074 |
rs79347679 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514062 | AGCGAAGGGTCCTCT[A/C]ACTGCCACAGAACGA | 2074 |
rs79490275 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536449 | CAACACATCTTTCTC[A/G]GACTCTGGCAGAAGG | 2074 |
rs79526894 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529496 | CACATCAATTTCACA[C/T]GCTCCCACAAGAGAC | 2074 |
rs79543342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497198 | CTCCCCAAGGAGAGT[A/G]GGACTCTGCCTGGCC | 2074 |
rs79789545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533821 | AATTTAAAGTTTTTT[A/T]AAAAGATTAATTAAA | 2074 |
rs79859389 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537423 | CACCAGGCAATGTAC[C/T]AGGTTAACTAATTCC | 2074 |
rs79893651 | snp | A/G | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525494 | TGAAGACATTACACC[A/G]TAAGTGTAAAGTCAC | 2074 |
rs80105100 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461923 | ACTATCAGACTTAAA[C/T]AAACAGAAAGACATC | 2074 |
rs80133923 | snp | C/T | 0.00199136 | 0.0314915 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532815 | GGACAGCCCGTCACC[C/T]ACAGAACGAAAGGAG | 2074 |
rs80202965 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477651 | AGCCTCCCCAGTCTT[C/G]CCAGCTAGCTCCTCC | 2074 |
rs80270486 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492363 | TGCTGCTTCTCCCCA[A/G]TAATGTAACCTGCAA | 2074 |
rs80273785 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540349 | CGGCTTGTAACTTGC[C/T]TTTTTTTTTTTTTAA | 2074 |
rs80286706 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49509224 | GTCACATATAAAGCA[A/C]CTTAGCACAGAACCT | 2074 |
rs80321478 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523581 | TTATTCTTTCTATGC[C/T]AAAGCTTAAGTTTCA | 2074 |
rs111242827 | snp | A/C | 0.0517044 | 0.152246 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517804 | CTGCCTTGGCCTCCT[A/C]AAGTGCTGGGATTAC | 2074 |
rs111317675 | snp | A/G | | | missense | ERCC6 | GRCh38.p7 | 10:49470500 | TTTCTCTTTTGTAAG[A/G]AAGACCTAACTTTTC | 2074 |
rs111332057 | snp | C/G | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461802 | AAAATATAATGGTGG[C/G]AAAATTCTATTTACA | 2074 |
rs111339748 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490075 | AACTTTTATTAAATG[C/T]GATTTCAAGTGACCA | 2074 |
rs111347056 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504117 | GTCAATTCAATTCCA[C/T]AGAATGCAGCAAATA | 2074 |
rs111349376 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481014 | ATTAATGTTAAACTT[C/T]GTTCTGATTTTGTTG | 2074 |
rs111350679 | snp | A/G/T | 0.00398731 | 0.0445001 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465188 | GCGTGACCTGGATGC[A/G/T]AGACAAGGAGTCAAA | 2074 |
rs111352374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495325 | CATCACAGGGCCACA[C/G]GCCTGCCTCTCACAC | 2074 |
rs111409020 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512445 | GTGTGTTCAAAGGAG[A/G]AATAATTACATTTCT | 2074 |
rs111427558 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478268 | CATACCTCACCAGAC[C/T]CTCTCATCCGCAGAG | 2074 |
rs111442415 | snp | G/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507436 | ACAACAGTTTAATAA[G/T]TGATACTTTTTATAA | 2074 |
rs111449393 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510222 | ACCTATTAGGGTGCC[A/G]CATCAATGGAACCCT | 2074 |
rs111488771 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526139 | TATATATATATATAT[A/T]TATATATATATATAT | 2074 |
rs111500316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528939 | CAACAGGCCATAAGA[C/T]AAGAAATAAAAACAC | 2074 |
rs111520056 | in-del | -/T | 0.5 | 0 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520681 | AGGAACTGCACACTC[-/T]TTCCCAATCCACCCA | 2074 |
rs111528908 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487824 | CTTCCTGTGTTCAGG[A/G]AGATGTATTAATGAT | 2074 |
rs111565031 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474316 | AGGCAAGGAGGCTGT[C/T]TAACCTATAACACAG | 2074 |
rs111589375 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49461905 | ACACTCCTGGGAAGA[C/T]AGACTATCAGACTTA | 2074 |
rs111604526 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456958 | GCTCCTACTGCATTA[C/T]AGCTTTTGATAGTAT | 2074 |
rs111647939 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508150 | ACCTTGGAAGAATCA[C/T]AGCCACTTAAACATA | 2074 |
rs111658469 | snp | A/G | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528814 | AGCCCTTAAATACAT[A/G]GGCACTGACCTGAAA | 2074 |
rs111665120 | snp | A/C | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536814 | ATGGTAGCGCAAAAG[A/C]GTCACGGGGTTGAAG | 2074 |
rs111688132 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534242 | TAGATAAATCCAATA[C/T]AGACAAGGAGAAGGA | 2074 |
rs111688206 | snp | A/G | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489720 | AAGCAATTTATCATT[A/G]TGTATCTTCCAATAA | 2074 |
rs111689031 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479880 | ATAAAAACACAAGGT[A/G]GGGATTCAGCTAGAT | 2074 |
rs111696205 | snp | A/C/T | 0.5 | 0 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522329 | TCTTTCATCCCCCAA[A/C/T]CCAAACAGCACCAAA | 2074 |
rs111705140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536143 | AAAGTTTCAGTGGAG[C/T]GATAGGGCCAAAAAC | 2074 |
rs111719182 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462217 | TAGAAATAGATTGAA[C/T]TGCATTTGGAAATGT | 2074 |
rs111879751 | snp | A/G | | | missense | ERCC6 | GRCh38.p7 | 10:49474052 | TGAGAAAACAGCAAT[A/G]CTCGCTGACCCTGCT | 2074 |
rs111916305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479895 | GGGGATTCAGCTAGA[G/T]TTCTCTACCAATGCT | 2074 |
rs111918245 | snp | A/G | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509264 | AGTGCTTAATAAACT[A/G]CTATAGTATTATATA | 2074 |
rs111950756 | snp | A/C | 0.5 | 0 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482846 | GCCAGACAGAATGAT[A/C]CGATGAGGGGTGCGA | 2074 |
rs112009143 | snp | A/G | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505041 | AAACTTAATCATCTC[A/G]AACAAAGAACTTTGC | 2074 |
rs112059539 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458550 | CCAAGGAGTAACTGT[C/T]AGGTACCTGATTTAC | 2074 |
rs112062630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49465240 | AGATTTGACTGCCCT[A/G]CTGGACTTCAGACTT | 2074 |
rs112067509 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506079 | TTAAAAAGATAGCTC[C/T]TGATAATGTACAAGA | 2074 |
rs112090508 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526131 | TTTATATATATATAT[A/T]TATATATATATATAT | 2074 |
rs112162869 | in-del | -/AACA | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510414 | CCAAATCCTTCCCCT[-/AACA]TACATATCCACACAT | 2074 |
rs112172840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497172 | CAGGGCCTGTCCAGG[C/T]GCCCCTTGAGCTCCC | 2074 |
rs112219023 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487677 | ACAGTTACCAAATGA[C/G]ACACCAAGCTTCCCA | 2074 |
rs112228268 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530586 | AACATACAAAAGAAA[C/T]CCAAAATTTCTCTAT | 2074 |
rs112249028 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454745 | ATATCAATATATACC[A/C/G]GAAAAGACTTTGAGG | 2074 |
rs112294552 | snp | A/G | 0 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479217 | ATCTAAATAGGCTTA[A/G]CAACTTAGTAAATTA | 2074 |
rs112304654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474915 | GCCTTGAGAGGATGA[C/T]TCAAATCAAACTCAC | 2074 |
rs112314975 | snp | A/G | 0.000742507 | 0.0192536 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49493138 | GTGGGTATAGGAACC[A/G]GTTTCATGTAGAATT | 2074 |
rs112475110 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463812 | CCGTCCATGTAAGAT[A/G]TGACTTGCTCCTCCT | 2074 |
rs112545243 | snp | A/G | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477673 | AGCTCCTCCTCTTCT[A/G]CCCTCCTCCTTGCTC | 2074 |
rs112571332 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462419 | GTAGTACAAGAAAAC[A/G]TGGCGAATTATCATA | 2074 |
rs112621987 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505535 | ATATGCAACTCTTCC[C/T]ATTAATCTTATTTAA | 2074 |
rs112644868 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536031 | TGAGGCACGAGAATC[G/T]CTTGAACCCAGGAGG | 2074 |
rs112680086 | snp | A/G | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503582 | CACAGCTGGTAGATG[A/G]TATACATAGCTGGTG | 2074 |
rs112742944 | snp | C/T | 0.00135469 | 0.0259906 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482913 | TTACCTTTTAGCAAT[C/T]GCCATTCCTACCCTA | 2074 |
rs112798847 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493955 | TGTGGGCAGGTAGTT[C/G/T]GGCAGCAAAATCAAG | 2074 |
rs112805069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495758 | AGCAACCTACACTGA[C/G]TTCACATCATTTTTA | 2074 |
rs112848557 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49474843 | GACAAGGGGTGAGTG[C/T]CCCGGCCCATCCCCA | 2074 |
rs112884226 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489576 | TGTTGCTTTTCCCAC[C/T]CTTATGCATCTACAT | 2074 |
rs112905576 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481078 | TTTGGAAATACACAC[C/T]GAGGGATTTGGAGAA | 2074 |
rs112940372 | snp | A/G | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511276 | AGAATTCTTATGATG[A/G]GAAAAAAGTCTAGAC | 2074 |
rs113010035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49492612 | TGAAGAAATACAACT[A/G]TCAATACATGACGAT | 2074 |
rs113028250 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525223 | AACAGGGATCACCAT[A/G]TACCTAAAAAGGAAA | 2074 |
rs113059414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464741 | CTGTGGCTTCAGATG[A/G]TGCAAGCCCCAAGCC | 2074 |
rs113074110 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484263 | TCCAGCCTGGGTGAC[A/G]GTCAGACTCTGCCTC | 2074 |
rs113193671 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491444 | CAAGTTAGAGTCCTT[C/G]GTAAACTGTAAAACA | 2074 |
rs113196138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514988 | AAATTAAGACTGATA[C/T]AGACAATTATGCCCA | 2074 |
rs113258955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538691 | GACCCTGCGCGCAGG[A/G]GGCCTTATACAAAGT | 2074 |
rs113260026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529584 | GACCTTTGGGCTGCT[A/C]TTCTGGAAGCAAGTG | 2074 |
rs113282441 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507146 | AAAACCACACAGAGC[C/T]CAATGCTAGTATGTA | 2074 |
rs113343547 | snp | A/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510155 | TCAGAAGCAACTCAG[A/T]CCCAGCACAACCAGT | 2074 |
rs113344615 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531978 | CTTCTTCCCCATTAA[C/T]GTGCTATGCTCAAAA | 2074 |
rs113372945 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487054 | CACAATCATCTAATA[C/T]AAATTTTATAAAATT | 2074 |
rs113373426 | snp | A/G | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529658 | GTATAATAAAAGGAG[A/G]GCCACGTGAACTGAA | 2074 |
rs113374745 | snp | G/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49526563 | TGAACAGAAGTTCTT[G/T]GTTTTATATATAGTC | 2074 |
rs113444430 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455630 | TGGTGGAGAAAAGAA[A/T]ATTTGTTGATCATTG | 2074 |
rs113463724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504358 | ATTTTTAAAAAACGA[A/C]TATTATTTATATTAA | 2074 |
rs113464314 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490949 | TAGAGGACGAATCAC[C/T]ACAAACAGAATTTTT | 2074 |
rs113475819 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476562 | CTGGCTTCCTGCTCA[C/T]GGGCAAGTTCAGTGC | 2074 |
rs113493440 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49534149 | AAAAAAAAAAAAAAA[A/C]AAAAACAAAAAAAAA | 2074 |
rs113515150 | in-del | -/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537718 | AAACAACGTGTGAAA[-/T]TTTTTTTTTTTTTTG | 2074 |
rs113540214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503422 | TCTTACTAGGCAGCA[C/T]GTAAGTCATATCTCT | 2074 |
rs113584187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49483218 | ATTAAGGAAAATGCA[C/T]ATTTTAAATTTCTTG | 2074 |
rs113663657 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539725 | AGGAAGTTGAGCTTC[G/T]CCTGGGGAAAGAAGC | 2074 |
rs113671221 | snp | C/G | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464308 | AGAGAGATGATTTAG[C/G]GTATCTGGCGGAAGA | 2074 |
rs113692507 | snp | C/G | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533862 | AAATAGGCTGGGCAC[C/G]ATGGCTCACATCTGT | 2074 |
rs113730266 | snp | A/G | 0.000310607 | 0.0124582 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472864 | GCTAACCATGAAACT[A/G]TATTTCTACTAATAC | 2074 |
rs113742572 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458139 | GAAAAAGATGCCCTC[C/T]GCTTAAAGGAAAGCC | 2074 |
rs113753075 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500375 | TGCCCTACAGCTCCA[C/T]TGTCTCGTAAAATTT | 2074 |
rs113763776 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489967 | TGCAGTGTTTATTGT[C/T]GTTTTAACAAATAAA | 2074 |
rs113768084 | snp | C/T | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505706 | TTAGTCAACTTATTA[C/T]CATCCAATTTTAATG | 2074 |
rs113870278 | snp | A/C | 0.5 | 0 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520695 | TTCCCAATCCACCCA[A/C]ACAGGGCCTCGGAGC | 2074 |
rs113887203 | snp | A/G | 0.000345898 | 0.0131465 | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524635 | GCCTGATGCTTCATT[A/G]AGCATGATTTTTCTG | 2074 |
rs113936879 | in-del | -/T | 0.5 | 0 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521868 | TTGACGGAAAATTCC[-/T]AGTAAGTATCAGCTA | 2074 |
rs113943228 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493444 | TAAAATCTCCATAAT[C/T]TCATTCATCAATTAG | 2074 |
rs113944820 | snp | A/C | 0.5 | 0 | missense | ERCC6 | GRCh38.p7 | 10:49470322 | TCAAACTTGGCGTCT[A/C]TGCAATGCTTAGAGT | 2074 |
rs113959020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496990 | ACCCTTATACTCCAA[C/T]GTAACAAAATAACCT | 2074 |
rs113974179 | snp | A/C | 0.5 | 0 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504891 | TACTCTTCACTCTCC[A/C]CTACCCCAATGGAGA | 2074 |
rs114028287 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49526088 | TTTTGGTTTTATTTA[C/T]ATTTATATATTTATA | 2074 |
rs114093805 | snp | A/G | 4.95602e-05 | 0.00497771 | missense | ERCC6 | GRCh38.p7 | 10:49472995 | CTAAGCCGCCCACCC[A/G]CGTGGTCAGAAGAAA | 2074 |
rs114143901 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468115 | CAGACATGTTTCCTC[C/T]AATTCGAAAAGTTAA | 2074 |
rs114150693 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522205 | GTCTTTCTGTTTCTC[A/G]AGGGAATAGCATTAC | 2074 |
rs114159712 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ERCC6 | GRCh38.p7 | 10:49470062 | ATCTAAATTTTTGAA[C/G]AAAAACACTAATGGC | 2074 |
rs114183603 | snp | A/G | 0.00874735 | 0.0655527 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456660 | TTTAATTTTTTGACA[A/G]AATTTTAAAATCCTT | 2074 |
rs114234514 | snp | C/T | 0.00141582 | 0.0265689 | missense | ERCC6 | GRCh38.p7 | 10:49470215 | TTTCCAAAACATAAT[C/T]GTCATTGCTCTGTTC | 2074 |
rs114364247 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510861 | AGCCTACCTCTTGCT[C/G]CATTTCCTACTCCTT | 2074 |
rs114369077 | snp | A/G | 4.94181e-05 | 0.00497057 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532707 | CTCAAGGGCCTGGGC[A/G]CTAGGCTCTACTGCC | 2074 |
rs114385558 | snp | A/C/T | 0.0154538 | 0.0865337 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518562 | TGTGCACCACTCCCG[A/C/T]CCCTGCCCCCACCTC | 2074 |
rs114403790 | snp | C/T | 0.000115341 | 0.00759324 | missense | ERCC6 | GRCh38.p7 | 10:49458867 | CCACCAGAAGTTCTA[C/T]GGAAAGTGCACAGAT | 2074 |
rs114423177 | snp | A/C/T | 0.00026355 | 0.0114767 | missense | ERCC6 | GRCh38.p7 | 10:49478449 | CTCGTAAGACACATG[A/C/T]ACACTTGTAAGCAGT | 2074 |
rs114479292 | snp | C/T | 0.000559975 | 0.0167235 | missense | ERCC6 | GRCh38.p7 | 10:49470379 | TGTTTCTCCAGGGTC[C/T]CTTCTTCTGCCACAC | 2074 |
rs114484032 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499807 | GCTTATTCTTCTGGA[A/T]TACAAAAGCCTTAAT | 2074 |
rs114490473 | snp | A/G | 0.00024751 | 0.0111218 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49476260 | TTCTTTGGAATCAAC[A/G]AAATTTTGGTAGACT | 2074 |
rs114539132 | snp | A/G | 0.00194706 | 0.0311407 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478519 | ATATGTTTAAGGAAC[A/G]CATTTGTTCTTACCT | 2074 |
rs114662249 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513142 | ATCTTATACATATCA[C/T]CACCCATGAAGAAGG | 2074 |
rs114694744 | snp | A/G | 0.000131811 | 0.00811715 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49459139 | AGCCAAGAGTGAGGA[A/G]GAAGCGAGGGGCCCG | 2074 |
rs114723899 | snp | C/T | 0.0263992 | 0.111815 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456678 | TTTTAAAATCCTTTA[C/T]TTGTGCTGATAAAGC | 2074 |
rs114768774 | snp | A/G | 4.94654e-05 | 0.00497295 | missense | ERCC6 | GRCh38.p7 | 10:49532561 | AGGTCATCCAGGACC[A/G]ACCGATACTCCTTCT | 2074 |
rs114832108 | snp | A/G | 0.00056039 | 0.0167296 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482732 | CATGGTGATGGGGAC[A/G]GAGAACTGCTCCATA | 2074 |
rs114852424 | snp | A/G | 0.000247164 | 0.011114 | missense | ERCC6 | GRCh38.p7 | 10:49482775 | GTGCCTAACTTTCCC[A/G]GGAAGATGAAGTCAA | 2074 |
rs114883603 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508605 | CAAGTATTTGTATCA[C/T]TGTGAAGACAAATTG | 2074 |
rs114885927 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529235 | TTCAAATACGAGTGT[C/G]GGACAAGGGGAAATC | 2074 |
rs114896216 | snp | A/G | 0.00145867 | 0.0269668 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474222 | GCAAATTTTTCTTAG[A/G]GCTATAAGTCCGGAG | 2074 |
rs114955363 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499218 | ACAACAACAACACGA[C/T]GTTTAGCATTTAAAA | 2074 |
rs114988459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497788 | TTAATCTTTGATTAC[C/T]ATTGATTACCTAATA | 2074 |
rs115095595 | snp | A/G | 0.00913223 | 0.0669531 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49500570 | AGTCCTGATCTTGCT[A/G]TAGCTCAGACCTGCC | 2074 |
rs115100965 | snp | C/T | 0.000117595 | 0.00766704 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472918 | ACAAACCTGCGTGTC[C/T]GTGCTTGGGTTCCAG | 2074 |
rs115162931 | snp | C/T | 0.00266329 | 0.0363944 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516270 | CGAATAAATTGTTTG[C/T]ACCCGTGACGACCAA | 2074 |
rs115185216 | snp | A/G | 6.58946e-05 | 0.0057396 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532782 | CGGAGCTGCTGATGC[A/G]CACCCCACAGCAGAG | 2074 |
rs115249401 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479188 | GTCAATAAATTATTG[C/T]TACTTCAAAAAAAAT | 2074 |
rs115251077 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | ERCC6 | GRCh38.p7 | 10:49532742 | TCTGATGTCGGTCGA[C/T]GTGCAGCAGGGCTGG | 2074 |
rs115281814 | snp | A/G | 0.0166325 | 0.0896639 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456943 | AACAAGGACCACCTT[A/G]CTCCTACTGCATTAT | 2074 |
rs115312898 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528071 | CCATTCTACAAATGC[A/G]ATTAATGATGTTGGG | 2074 |
rs115319252 | snp | A/C/T | 0.000163825 | 0.00904919 | missense | ERCC6 | GRCh38.p7 | 10:49461551 | TCATGACACTGTGCA[A/C/T]GCCAACTAGCAAGAA | 2074 |
rs115385326 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505597 | AAGAACAAAAAAATT[A/G]TTCAACATAAATGGC | 2074 |
rs115446859 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512510 | ATATTTTATCATTAA[A/G]TGGGCCTTAAGCTTA | 2074 |
rs115522942 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507048 | TAAGAGAGAATGTCC[A/G]AGGGAAGGCAAGAGA | 2074 |
rs115560123 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49472849 | AGGACAGTCAAAAGC[A/G]CTAACCATGAAACTA | 2074 |
rs115580386 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475394 | GTGTAGTTTGCATTC[C/T]CTTTCCTGGATAGTG | 2074 |
rs115582915 | snp | A/G | 4.94637e-05 | 0.00497287 | missense | ERCC6 | GRCh38.p7 | 10:49500554 | TGTAATTTGAACCAC[A/G]AGTCCTGATCTTGCT | 2074 |
rs115593504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ERCC6, PGBD3 | GRCh38.p7 | 10:49514869 | TTGAGATACTTGGTG[C/T]TTTACTTTTCTTATC | 2074 |
rs115604255 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525650 | GCCAATGATACCCAG[C/T]TTTTCATTAAACTTG | 2074 |
rs115633798 | snp | C/T | 0.000214995 | 0.0103659 | missense | ERCC6 | GRCh38.p7 | 10:49460396 | TCTCTGTTGGAGATG[C/T]TGATGAAGGATGCTG | 2074 |
rs115643329 | snp | C/T | 0.000214135 | 0.0103451 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524544 | GGGCTGGAGCTTTTC[C/T]AGCTGCTCTTTTATT | 2074 |
rs115677159 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520926 | GGGCAAATGCGTAAC[A/G]TTGTTAATTTGGATA | 2074 |
rs115686725 | snp | A/C/T | 3.42843e-05 | 0.00414019 | missense | ERCC6 | GRCh38.p7 | 10:49461517 | TCTGGGCTGGCTCCA[A/C/T]CCATGATGGCATCGT | 2074 |
rs115698897 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | ERCC6 | GRCh38.p7 | 10:49470524 | ACTTTTCATCAATGC[C/T]TTCATCACCAGATGG | 2074 |
rs115746084 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508808 | TAAAGATGGGGCCGA[C/G]AAGTACACCACAACA | 2074 |
rs115747823 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502824 | GTCCCCACAGCAACA[A/G]ATTATTTAGCCCTAA | 2074 |
rs115788540 | snp | C/T | 1.64988e-05 | 0.00287213 | missense | ERCC6 | GRCh38.p7 | 10:49474167 | CATCAGGAAGACCTT[C/T]GAGATTCTTGGGACC | 2074 |
rs115848378 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462940 | TTACATATGTGTTTA[C/T]CTTTTGATCTAGCAA | 2074 |
rs115875661 | snp | A/G | 0.000494413 | 0.015715 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474146 | ACTGATCTTCTTCTA[A/G]TTCATCATCAGGAAG | 2074 |
rs115876786 | snp | A/G | 0.000329946 | 0.0128399 | missense | ERCC6 | GRCh38.p7 | 10:49493166 | ATTGCCACTCTGAAC[A/G]GAGGCCACCACGTGT | 2074 |
rs115921414 | snp | A/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, utr-variant-5-prime | ERCC6 | GRCh38.p7 | 10:49539490 | CTGAACACGGGAAGG[A/T]TGGAGAGCTGTCCTG | 2074 |
rs115975145 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536144 | AAGTTTCAGTGGAGC[A/G]ATAGGGCCAAAAACC | 2074 |
rs115983952 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481966 | GGAACCCCTGAGAAC[A/C]AGCATCCTCCAGAGT | 2074 |
rs116032070 | snp | A/G | 0.0010612 | 0.0230102 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49461531 | ATCCATGATGGCATC[A/G]TGCTTCATGACACTG | 2074 |
rs116095044 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49463775 | ATGGGAGTTTTCCTG[C/T]ATAAGCTCTCTTTGC | 2074 |
rs116178464 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502977 | TGATGTGCAATTAGT[C/T]TCCAGAATCACTACA | 2074 |
rs116186885 | snp | C/T | 0.000131893 | 0.00811969 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49472435 | GTACACAGTCACTTG[C/T]TTCTTCTGGCCTATT | 2074 |
rs116249338 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471835 | TAAAGTCTGTGGTGG[A/G]GGAGTGGGAGAAGCT | 2074 |
rs116263349 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512346 | AACTGTGAGAAACCA[C/T]ACTGCAATCCTGACC | 2074 |
rs116267514 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505297 | CCAATGCTTGGCCAC[C/T]TACACATGAAACCTG | 2074 |
rs116275562 | snp | C/T | 0.000444851 | 0.0149073 | missense | ERCC6 | GRCh38.p7 | 10:49532586 | CCTTCTCCACGTCAA[C/T]GAGCTGGGAGGCACG | 2074 |
rs116300362 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531917 | CCCCTCCCACTTCCC[C/T]TCTCCTGTCCTCACC | 2074 |
rs116360202 | snp | C/T | 0.00228846 | 0.033749 | missense | ERCC6 | GRCh38.p7 | 10:49532580 | GATACTCCTTCTCCA[C/T]GTCAACGAGCTGGGA | 2074 |
rs116371381 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508045 | GAGTTTACATAATGA[A/G]AGAGTCCTCGGTATC | 2074 |
rs116373975 | snp | A/C | 0.000445078 | 0.0149111 | missense | ERCC6 | GRCh38.p7 | 10:49500564 | ACCACGAGTCCTGAT[A/C]TTGCTGTAGCTCAGA | 2074 |
rs116405364 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533531 | CTCAGTCCTGTAATC[C/T]CAGCACTTTGGGAGG | 2074 |
rs116417950 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530101 | TTAGAGGAAGCAAGG[A/G]CTAAGCAGAAAAGAG | 2074 |
rs116431130 | snp | A/C/T | 4.94208e-05 | 0.00497075 | missense | ERCC6 | GRCh38.p7 | 10:49473541 | CCATCCATCTTGAGA[A/C/T]AGGTATACTTTTGGG | 2074 |
rs116454828 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518141 | AGGTGCTAGACAGAA[A/G]GGAGAAGTTCCCAGA | 2074 |
rs116532513 | snp | A/C | 0.00947846 | 0.0681864 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532812 | GGTGGACAGCCCGTC[A/C]CCCACAGAACGAAAG | 2074 |
rs116576048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510221 | AACCTATTAGGGTGC[C/T]GCATCAATGGAACCC | 2074 |
rs116592706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488373 | TCCTAGGCAGGATTT[A/C]CTGCACCTGTAATTA | 2074 |
rs116610439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49496200 | GCCTTCCCTGTCCCT[G/T]TCTCTGTAAACAAGT | 2074 |
rs116645710 | snp | A/G | 0.00913223 | 0.0669531 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470396 | TTCTTCTGCCACACT[A/G]TGATGTTTTGTTTTT | 2074 |
rs116660513 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524083 | ATCTCGGTATCTTCC[C/T]ACTTTCCGACCTCCT | 2074 |
rs116683200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517327 | CAGTAAAGTTATATG[C/T]ACCTGTCTTTGGATA | 2074 |
rs116698997 | snp | C/G | 4.94784e-05 | 0.00497361 | missense | ERCC6 | GRCh38.p7 | 10:49532556 | ACGTGAGGTCATCCA[C/G]GACCGACCGATACTC | 2074 |
rs116715649 | snp | A/G | 0.000132433 | 0.00813627 | missense | ERCC6 | GRCh38.p7 | 10:49460420 | GATGCTGCACAGAGA[A/G]GTTAGAATTCCTTTT | 2074 |
rs116733341 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524108 | CCTCCTCCTCCTCCT[C/T]CTCCTACAGAAGCAG | 2074 |
rs116768350 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466086 | CCTAAAGTGGAATAC[A/T]AACAAATAAATTAAC | 2074 |
rs116768954 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513079 | TTTAGCTAGTGGGCA[G/T]GTAACAAGAATAGCT | 2074 |
rs116802319 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537884 | TATGCCATCATGCCC[A/G]GCTAATTTTTCGTAT | 2074 |
rs116820384 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528267 | TCTGCAGGTGTAGAG[A/T]ATAAAATTTTCCTAA | 2074 |
rs116896972 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523501 | ACACTTTTTGCATGA[C/T]GGTGGCTTATAATTA | 2074 |
rs116908357 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49501592 | AGAGTGGAAGAAACA[C/T]TTAACAACAGGGAAT | 2074 |
rs117007867 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510082 | CCCTACATTCAGGTA[A/G]GAATGAGAATCTGGC | 2074 |
rs117070216 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478812 | AGACTTACTGGGTTC[C/T]TGACCACCAGCCCTA | 2074 |
rs117121642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507686 | CCACCCTGGGGTAAT[C/T]TGACAATGCCCAGAG | 2074 |
rs117215329 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522298 | AATATGCTTCTCAAT[C/T]CTGAGCATTTTATTT | 2074 |
rs117222844 | snp | A/G | 9.88452e-05 | 0.00702942 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49483400 | AATTTTGTGTCCTTC[A/G]TCCAAGATCACATAG | 2074 |
rs117289374 | snp | C/T | 0.0103295 | 0.0711199 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49457488 | GTCCGGCAAGGCCCC[C/T]CTGCCCAGAACCCTC | 2074 |
rs117525685 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467522 | TACATATCTTTCTTG[C/G]TGAAGTCTGTTCAAA | 2074 |
rs117553393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538577 | ACACTCTTATCAATT[C/T]GACTCTATCAACGCC | 2074 |
rs117553576 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523143 | AACTGTTGAGGATTG[A/G]GAAAAAGCCATCCCA | 2074 |
rs117555054 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454725 | CCAAGAAAAGCTATA[C/T]AATTATATCAATATA | 2074 |
rs117690234 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ERCC6 | GRCh38.p7 | 10:49500240 | TGAGTTTGTAAACAA[C/T]CCCTTTGTAGAAGCT | 2074 |
rs117704592 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533380 | AAGATCAACTGTAAT[A/G]CATAGGAACAGCGAT | 2074 |
rs117766317 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475699 | TAAATAAATTACTGT[C/T]CTACCCTGGGGACAA | 2074 |
rs117820507 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507510 | TCTTCTTCTCCACTG[A/G]TATTTTTTTTCCTTA | 2074 |
rs117992505 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464498 | AGAAATTTGCATTAC[A/G]TAACGAGGAGCCAAA | 2074 |
rs118095088 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456562 | ACCTAGGGCTGTACT[G/T]AGCTGTGGAACAGGT | 2074 |
rs118156498 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497787 | TTTAATCTTTGATTA[C/T]CATTGATTACCTAAT | 2074 |
rs121917900 | snp | A/G | | | stop-gained | ERCC6 | GRCh38.p7 | 10:49500673 | AGACAGGTGTTAGGT[A/G]GCTGTGGGAATTGCA | 2074 |
rs121917901 | snp | C/T | 0.0001812 | 0.00951667 | ERCC6 | 10 | allele_origin=T(germline)/C(germline) | 10:49478437 | TGTGCATGTGTCTTA[C/T]GAGATACCATAAATC | 2074 |
rs121917902 | snp | C/T | | | stop-gained, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524073 | AAAGTGGGAAGATAC[C/T]GAGATGATGGAGATG | 2074 |
rs121917903 | snp | C/T | | | stop-gained | ERCC6 | GRCh38.p7 | 10:49532736 | CTGCTGCACATCGAC[C/T]GACATCAGATCCAGG | 2074 |
rs121917904 | snp | C/T | 6.59163e-05 | 0.00574054 | ERCC6 | 10 | allele_origin=T(germline)/C(germline) | 10:49482809 | ATGCAAAATAACCTC[C/T]GAGAGCTGTGGTCGC | 2074 |
rs121917905 | snp | C/T | | | missense | ERCC6 | GRCh38.p7 | 10:49471085 | TGACAAATAGAGTGC[C/T]AAAAGACCCAAAACA | 2074 |
rs137879476 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525971 | ATCCTTACTGTTGAA[A/T]GTAGCTGTAGTTTGT | 2074 |
rs137940039 | snp | C/T | 0.000153988 | 0.00877328 | missense | ERCC6 | GRCh38.p7 | 10:49474227 | TTTTTCTTAGGGCTA[C/T]AAGTCCGGAGAAAAT | 2074 |
rs137941107 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529067 | ATATATCTTGCCATG[C/T]CTCTCCACCCTGGCC | 2074 |
rs138008904 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479950 | GACAACTTGCTGAGC[A/G]TGCCCATGCTCCTTC | 2074 |
rs138059408 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533393 | ATGCATAGGAACAGC[A/G]ATGTTAGGAAAGAGC | 2074 |
rs138074935 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464527 | AATGTTAATCCCCAA[A/G]ACAATGAGGAAAATG | 2074 |
rs138117257 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512613 | CTATGCCTATGATAC[A/G]TTGAACAGCCCTTAT | 2074 |
rs138119967 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538285 | AAGGGCCAAATCACA[C/T]AAGGCCTGGGAAAAC | 2074 |
rs138372416 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519587 | GGAGACTCAGGCACC[A/G]CCTACTGAAGAGTCC | 2074 |
rs138443493 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482425 | AGGAACAATGCCAAA[A/T]CTGTTTAATTTCCAT | 2074 |
rs138444551 | snp | A/G | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49525246 | AAAGGAAAAACATAA[A/G]TGTCAGCTCTATGCT | 2074 |
rs138507121 | in-del | -/CTGG | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49495623 | GCCATCCTCCCCTAC[-/CTGG]CTGTCCCCTGTCCCC | 2074 |
rs138534983 | snp | A/G | 0.000840288 | 0.0204802 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515967 | TCTGATTCCAGTGGA[A/G]CTCTGTCAATGTGAT | 2074 |
rs138563314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507724 | TGGTTGTTAGAACTG[C/T]GGAAGGAGTCGGGAG | 2074 |
rs138599269 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456694 | TTGTGCTGATAAAGC[A/T]TGTTAAATACATTAA | 2074 |
rs138649908 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538631 | CCCGACTCTCTTTAA[A/G]ATAACAGCTCCAGCA | 2074 |
rs138679291 | snp | A/C | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49469698 | TCACTAAGCAGGGCT[A/C]TCTATATACTCCATG | 2074 |
rs138707118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490274 | AGAGGTGGGAAGCTA[A/C]AGGGCAACTTGGGGA | 2074 |
rs138709324 | snp | C/T | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49488416 | TTCAAGCTAAATCTT[C/T]AATAAACAAGGATTT | 2074 |
rs138724131 | in-del | -/GATATATATACACTTTCCTGATACACATATCTGAATTCTT | 0.429837 | 0.173662 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507921 | CTTAGAAACTGAACA[lengthTooLong]GATATATATACACTT | 2074 |
rs138756386 | snp | A/G | 0.000593022 | 0.0172093 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49530825 | ATTGATTTGCCTTAG[A/G]GATGTCGTACATGAC | 2074 |
rs138758064 | snp | C/T | 0.000643474 | 0.0179255 | missense | ERCC6 | GRCh38.p7 | 10:49493137 | TGTGGGTATAGGAAC[C/T]GGTTTCATGTAGAAT | 2074 |
rs138822457 | snp | C/T | 0.000230943 | 0.0107433 | missense | ERCC6 | GRCh38.p7 | 10:49528504 | GCTTTTGTTTTGCAG[C/T]GATCTTTTTTAGCTG | 2074 |
rs138862363 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475257 | CTTTTTAATCATTTT[A/T]AATTTTTGATTACAT | 2074 |
rs138865542 | snp | C/T | 0.000510679 | 0.0159712 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524201 | TTCTGCCGTTTCCCG[C/T]CCTTGGGCAGAGGCT | 2074 |
rs138980917 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512749 | TTCATATATAACTTA[C/T]ACACATAGGCTGAAG | 2074 |
rs139007661 | snp | G/T | 0.00324554 | 0.0401527 | missense | ERCC6 | GRCh38.p7 | 10:49470838 | GCTCCAAAGGCTGGT[G/T]GAATCCTTCTTTTTA | 2074 |
rs139037125 | in-del | -/AAG | 0.296873 | 0.245566 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504193 | AAAACGCAATCATAA[-/AAG]AAAAATGGAGACTCT | 2074 |
rs139075451 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | ERCC6 | GRCh38.p7 | 10:49532759 | TGCAGCAGGGCTGGC[C/T]CTCTCCTCGGAGCTG | 2074 |
rs139075879 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509008 | CTGTATATAAACATC[C/T]TGGGTTTGACATATG | 2074 |
rs139120838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510535 | GGGCCCTCCCAATCC[C/T]GTGACATCTTGGACA | 2074 |
rs139138000 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512119 | AATGTCAAAACACCT[A/C]TTGCAGTCTTGAGCC | 2074 |
rs139161933 | snp | C/T | 0.000561288 | 0.016743 | missense | ERCC6 | GRCh38.p7 | 10:49505974 | TCCTCCAGCTTCAGA[C/T]GTTTCTCTTTGTCCT | 2074 |
rs139186843 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513663 | AAGCACAGGAAAAAC[G/T]TCCACTTTTAAAACC | 2074 |
rs139188695 | snp | C/T | 0.000198554 | 0.0099618 | missense | ERCC6 | GRCh38.p7 | 10:49461443 | GCTGACGAGAGAGCC[C/T]CAGTGCTTTCAGGGC | 2074 |
rs139270549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494020 | CCCAATAAAAACATT[C/T]ACACACTGGGATACA | 2074 |
rs139373406 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504078 | TTGTACCTTCTGACT[A/C]CCTTGTGTACAACTC | 2074 |
rs139446199 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49514000 | AATACTGTCTTCAAA[A/C]AAGTATTTTCCAAAC | 2074 |
rs139479086 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49467207 | TCATGTACAAGCCTT[C/T]GTATGGACATATTTT | 2074 |
rs139509516 | snp | A/C/T | 3.31198e-05 | 0.00406928 | missense | ERCC6 | GRCh38.p7 | 10:49461449 | GAGAGAGCCTCAGTG[A/C/T]TTTCAGGGCATCCTG | 2074 |
rs139550619 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521720 | AGGCAGGAGAAACAC[A/G]TGAGAAGGGGGAATA | 2074 |
rs139597916 | in-del | -/AGGT | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49502488 | GCACCAGGCCAGGTG[-/AGGT]GTTTGGACACAGCCT | 2074 |
rs139630773 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481753 | TCACAGCAAGCTTAG[A/C]CCCTACTCCATCTCC | 2074 |
rs139631078 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ERCC6 | GRCh38.p7 | 10:49534064 | ACTTGAACCCAGGAG[A/G]CGGAGGTTGCAGTGA | 2074 |
rs139652034 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466980 | GAGATGGAGTTTCAC[C/T]ATGTTGTCCAGGTTG | 2074 |
rs139712566 | snp | A/T | 1.64789e-05 | 0.0028704 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515487 | TAACGTGAGTCAATG[A/T]TACGCTTCTGAGGTC | 2074 |
rs139777593 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521363 | AGCAGCATGTAGGTG[C/T]TCACCGGGAACCCAC | 2074 |
rs139821232 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49459642 | CTGTGGATAAGGAAC[A/G]ATATCATAGCTATAC | 2074 |
rs139904905 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484392 | TGTCAGGCAGAGACA[C/T]TAAGAAAAAGACGCA | 2074 |
rs139913322 | snp | C/G | 0.000198183 | 0.00995251 | missense | ERCC6 | GRCh38.p7 | 10:49476232 | GCATCTCTCCATTGA[C/G]AATCCTGTAAACTTC | 2074 |
rs139921386 | snp | C/T | 1.6543e-05 | 0.00287597 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482693 | ATATTTTACCTGTAC[C/T]GGGGAAGCATTTGAA | 2074 |
rs139932923 | snp | C/T | 3.29685e-05 | 0.00405995 | missense | ERCC6 | GRCh38.p7 | 10:49470812 | TCTTGCGTTTTGGAA[C/T]ATCATGGTCTGCTCC | 2074 |
rs139949788 | snp | A/C | 0.00079348 | 0.0199025 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516492 | ACCAGTACATTATGC[A/C]CATCTGTTCTTTGTT | 2074 |
rs139989727 | snp | A/G | 0.000263626 | 0.011478 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515491 | GTGAGTCAATGTTAC[A/G]CTTCTGAGGTCTTCC | 2074 |
rs139990754 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531253 | CCTAAATATGCTTAA[A/T]CATTTTTTTATATAA | 2074 |
rs140038948 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49485012 | GATAGGCAAGGACTT[A/G]GAAGATCAGTCACCA | 2074 |
rs140114608 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49510175 | GCACAACCAGTTGAA[C/T]GACACCAGGAACAAT | 2074 |
rs140132694 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535845 | AAAGAAGTTTCAGGC[C/T]AGGCTTGGTGGCTCA | 2074 |
rs140135643 | snp | G/T | 4.94279e-05 | 0.00497107 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524051 | AACCGCTGCTTATAA[G/T]AATCTTCATCTCCAT | 2074 |
rs140181811 | snp | A/G | 0.00676609 | 0.0577691 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49454165 | TGTTCTTTGGAAAGC[A/G]TATCTCTCTTATTCT | 2074 |
rs140186496 | snp | A/G | 4.94376e-05 | 0.00497156 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532587 | CTTCTCCACGTCAAC[A/G]AGCTGGGAGGCACGG | 2074 |
rs140197978 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49539859 | GAGGGCAGTGACTGC[A/G]GGTCACTGCCTGGGA | 2074 |
rs140247973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480393 | CCCCTGCCATCATTT[C/T]AGCACCAGCATGACA | 2074 |
rs140248769 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455733 | AACATAACACTAATA[A/G]GCAATGTACGGTAGA | 2074 |
rs140260794 | snp | A/G | | | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516840 | TGCACAGTAAACGTA[A/G]ATGGAACTTCATCAG | 2074 |
rs140406992 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499726 | TACAGTTTAAATATG[G/T]AAGTGCTCATAGTAC | 2074 |
rs140496471 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527682 | ACTCTGTTTCAAAAA[C/T]ATACATATTTTTTTC | 2074 |
rs140604939 | snp | A/T | 0.000153988 | 0.00877328 | missense | ERCC6 | GRCh38.p7 | 10:49470517 | AGACCTAACTTTTCA[A/T]CAATGCTTTCATCAC | 2074 |
rs140611797 | snp | A/G | | | intron-variant | ERCC6 | GRCh38.p7 | 10:49487463 | CTTGGGGTGCACAAC[A/G]GCCTTAAAAACACAC | 2074 |
rs140694401 | in-del | -/ACAGC | 0.0905309 | 0.192535 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531323 | GAAGATTCACTTACT[-/ACAGC]ACTAAACTTTGTGGT | 2074 |
rs140717640 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523727 | GGGTGACTGTCGGTA[G/T]AAAGGCGACACAGCT | 2074 |
rs140738800 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516728 | ATCGTTTGGTGGTGC[C/T]GTAACTCTACCTGCT | 2074 |
rs140748987 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499346 | TCTGCTAACTTAACG[A/G]AAGAGTAAGAAATAA | 2074 |
rs140853588 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49507637 | TGGTGTACAACAATC[A/G]TTCTTGACAGGGGGC | 2074 |
rs140868411 | snp | A/G | 4.94295e-05 | 0.00497115 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516875 | GTCATCTTTAGGTGC[A/G]TATGAGGGATCATCT | 2074 |
rs140876119 | snp | A/G | 0.000230677 | 0.0107371 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49528439 | CTCCTCCAGACTGGC[A/G]TGATCTAGTTCAATT | 2074 |
rs140906145 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515864 | GGCAACAGTGACAAC[A/G]CTGTTATCATTCCAT | 2074 |
rs140927232 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517886 | CTCAGAGATGTTAAG[A/T]ACATTCTTAAAATAA | 2074 |
rs140991023 | snp | A/G/T | 3.29545e-05 | 0.00405911 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515683 | ACCATTTCTTTCCAC[A/G/T]GATTGATGCCCGATA | 2074 |
rs141034381 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ERCC6 | GRCh38.p7 | 10:49495960 | CTCTTGCGACAGAGA[C/T]TAAACACCTGGACGT | 2074 |
rs141080665 | in-del | -/AAG | 0.0123036 | 0.0774623 | intron-variant | ERCC6 | GRCh38.p7 | 10:49506852 | CACTTTCAAAATAAA[-/AAG]ATGATGTTTTCATTC | 2074 |
rs141121035 | snp | A/C | 0.00398564 | 0.0444627 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49456049 | TTGCATATAATATTA[A/C]ATGAAAAGTTAGTTG | 2074 |
rs141150537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49520238 | TGCCCGGTGACCCCA[C/T]GCTACACTTCCTAAG | 2074 |
rs141252710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528748 | CAGCAGACAGGCATG[A/C]CTGCACCCCCATGCT | 2074 |
rs141319934 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512025 | ACATAAATTTCAGAT[G/T]CTATAACAGTTGGCA | 2074 |
rs141372606 | snp | C/T | 9.88452e-05 | 0.00702942 | missense | ERCC6 | GRCh38.p7 | 10:49530733 | ACCTTATTATACTTC[C/T]GTCGTTTTACAGAAT | 2074 |
rs141391984 | snp | C/G | 0.00243635 | 0.0348177 | missense, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524272 | TGCCCCCTCCACCTC[C/G]TCATCTTCCTCCTCT | 2074 |
rs141513683 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479452 | GCGTAAATATTAAAA[C/T]AGGCTTTACTTTGAA | 2074 |
rs141542989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466539 | TGGTAAGTTGTGACA[C/T]TATGTACATACCATG | 2074 |
rs141650512 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ERCC6 | GRCh38.p7 | 10:49464770 | CCTTGGGAGCTTCCA[C/T]ACAGTGTTGAGCCTG | 2074 |
rs141660122 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513705 | TGAAAACTAACTATC[A/G]TGAGAACAGCATGGG | 2074 |
rs141723257 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490406 | GTCGCCCAGGCTAGA[A/G]TGCAGTGGCACAGTC | 2074 |
rs141732333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531444 | AATCTTCTTGATGAT[G/T]GTGTAATTTGCTGTT | 2074 |
rs141790086 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493761 | GCTGGCATGGCCCAG[G/T]TGACATGGCTACCAG | 2074 |
rs141800155 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489657 | TACAGAACTACTAGA[A/G]ACTACGTAGCAAAAA | 2074 |
rs141874502 | snp | C/T | 3.31071e-05 | 0.00406847 | missense | ERCC6 | GRCh38.p7 | 10:49500694 | ACACCTGTCTGCTGG[C/T]ACCTATGACAACAAA | 2074 |
rs142013483 | in-del | -/CCAT | 0.0517044 | 0.152246 | intron-variant | ERCC6 | GRCh38.p7 | 10:49487563 | CTGCCCAGAGAAAAA[-/CCAT]CCACCTTTAGCACCT | 2074 |
rs142020307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49459836 | CACATTAACTTAAAA[C/T]TGGAGTCTGAATCTG | 2074 |
rs142064684 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537237 | TAATCCCAGCTACTC[A/G]AGAGGCTGGGGCAGG | 2074 |
rs142067703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482484 | TTTCCTCTCTGTGAA[C/T]AGTTTTCATGATGTT | 2074 |
rs142094044 | snp | G/T | 0.00112137 | 0.0236522 | missense | ERCC6 | GRCh38.p7 | 10:49470479 | CTGTTTGAGCCTGGC[G/T]GGGTCTTTCTCTTTT | 2074 |
rs142097249 | snp | A/C/T | 0.00029652 | 0.0121731 | missense | ERCC6 | GRCh38.p7 | 10:49532621 | GCCTCATGGATGGCA[A/C/T]TGTCCACCTGCTGAA | 2074 |
rs142120142 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512868 | CCACTTGTGGCATCA[C/T]GTTGCTAAAAAATTT | 2074 |
rs142122327 | snp | G/T | 0.0142736 | 0.0832652 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455420 | AATTCTTGATTCAGC[G/T]GGAACAGAAAACACC | 2074 |
rs142131497 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49541003 | GCCATAACAAATGCC[A/G]TAGACTGGGCAGCTT | 2074 |
rs142135174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468653 | TGTACACAACAAACA[C/T]ATACACACACATACA | 2074 |
rs142185197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519497 | AGGGAGCCTTCAAAC[C/T]ATGCAGAGGAACCAA | 2074 |
rs142206454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511368 | TTTCTTTAATCTATA[C/G]ATGTAAAAGTCACAG | 2074 |
rs142219494 | snp | A/C | 0.000592924 | 0.0172079 | missense | ERCC6 | GRCh38.p7 | 10:49470241 | TGTTCCTTGGCCTCA[A/C]TCTTGTTTTCACTGT | 2074 |
rs142240023 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462925 | ACAAACAAAACAAAC[C/T]TACATATGTGTTTAC | 2074 |
rs142271727 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ERCC6 | GRCh38.p7 | 10:49486738 | ACAATGTGAAAAAGA[C/T]GTTATACTCTTCTCA | 2074 |
rs142476267 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ERCC6 | GRCh38.p7 | 10:49535038 | GGGGCCCAAGAAATA[C/T]CACGGAGGAACTGAG | 2074 |
rs142477138 | snp | C/T | 0.000576611 | 0.0169698 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515734 | CTCTGTCTACGCCTC[C/T]CATGAACTGGTTATA | 2074 |
rs142496478 | snp | A/G | 5.00371e-05 | 0.00500161 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524709 | TCATCTGGCCAGTGC[A/G]GATGAGCTCTTCCCA | 2074 |
rs142500584 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49488035 | GTTGAATATTATGGA[C/T]GGCTCTATCCAAACA | 2074 |
rs142561187 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533470 | CAGTAAATAGGAGCT[C/T]TGAACAAATCAGAAG | 2074 |
rs142580756 | snp | A/G/T | 0.00138654 | 0.0262938 | missense | ERCC6 | GRCh38.p7 | 10:49472997 | AAGCCGCCCACCCGC[A/G/T]TGGTCAGAAGAAACA | 2074 |
rs142582273 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49498768 | TTAATTTTTAGATCA[A/G]AACTACACTGCAGGG | 2074 |
rs142616577 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481352 | TTTTTAAAAAAAAGA[A/C]TGGTATAACAGGAGA | 2074 |
rs142625145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538482 | AAGCGAGGGCTGCCT[A/G]TCACAGGATGACAGC | 2074 |
rs142641602 | snp | A/G | 0.00083044 | 0.02036 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49474234 | TAGGGCTATAAGTCC[A/G]GAGAAAATCTGTGGT | 2074 |
rs142898326 | snp | C/T | 0.00181112 | 0.0300379 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516767 | TACAGTTAGGTCGGC[C/T]TTTTTCCATTTGCAA | 2074 |
rs142978212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509206 | GGAAGGATTAAATAA[A/G]GTGTCACATATAAAG | 2074 |
rs142978631 | snp | A/T | 0.0107246 | 0.0724382 | downstream-variant-500B | ERCC6 | GRCh38.p7 | 10:49453981 | GGAAGTTCACTAAGC[A/T]TCCTAGATGTTTTTC | 2074 |
rs142981983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491708 | CAAGCCATGATCCAG[C/G]TGAAGGTGTCCAATA | 2074 |
rs143030984 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531859 | TGACACTGCCCAGAA[A/C]ACTGCCCAACGGGGG | 2074 |
rs143045817 | snp | A/T | 1.65149e-05 | 0.00287353 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49458807 | GAAAGTTTAGGAAGC[A/T]ATGTTGTTTAGCAGT | 2074 |
rs143220639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49505730 | TTTAATGAACAGCAC[A/G]TGGCTATAATTTCAT | 2074 |
rs143260457 | snp | C/G | 0.000494087 | 0.0157099 | missense, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524572 | ATTACAACCTTGCTT[C/G]TTCCTTTCAAAAGAC | 2074 |
rs143305574 | snp | A/C/T | 0.000116271 | 0.00762387 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49517092 | AGGTCAGTTATTTCA[A/C/T]GTAAACTTAGTGTTC | 2074 |
rs143332960 | snp | C/T | 6.60338e-05 | 0.00574566 | missense | ERCC6 | GRCh38.p7 | 10:49476240 | CCATTGAGAATCCTG[C/T]AAACTTCTTTGGAAT | 2074 |
rs143334264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503794 | AGGGACAGTTAAAGA[C/T]TTTTATGAATATACA | 2074 |
rs143347263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528136 | TCTTTATCAAATTAA[C/T]AAAATAAGAATGTTT | 2074 |
rs143375792 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49512697 | CAATGAGATATGTTG[A/G/T]GATGGGACCCAAGAC | 2074 |
rs143380031 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49479045 | GAAAGGTCACTCTGC[C/T]CTAAAATGCAGCATA | 2074 |
rs143460768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49480030 | GGCAAGTCACCAGAA[C/T]GCTGAGAATCAAAAA | 2074 |
rs143502251 | snp | C/T | 3.29587e-05 | 0.00405934 | missense | ERCC6 | GRCh38.p7 | 10:49470638 | CATTTGTCTCTTCTC[C/T]AAGCCTATCATTGCT | 2074 |
rs143628801 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538091 | TTTGAGTTAAGAAGA[A/G]CAGAGAAGGGCTCCG | 2074 |
rs143694071 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49517478 | TGTGAAAAATCAGAC[C/T]TTGGCAATGACCTTG | 2074 |
rs143710725 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530002 | GTAACACCCAAGGTG[G/T]GAGGAAGGGCCAAGC | 2074 |
rs143723468 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503163 | CTCATCAACTTAACT[A/G]AAGTAGGGAGAGTGC | 2074 |
rs143758633 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49482340 | TACATGCTGTTCCAA[A/C]CTGATTTGTCCTTGT | 2074 |
rs143809689 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ERCC6 | GRCh38.p7 | 10:49494479 | TTAGACATAGGTATA[C/T]GTAGAAAAACTGGTT | 2074 |
rs143874111 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49503223 | AAATGGTAAACAGCA[C/T]AGGATCCCAAAAGGA | 2074 |
rs143923468 | snp | A/T | 6.59065e-05 | 0.00574012 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49516672 | TCGTCATCAAGAAAA[A/T]GTTCAAGAATTTCTG | 2074 |
rs143976179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49504603 | TTCCTTTTGCTAGTA[C/T]AACACTGATGGTATT | 2074 |
rs144019422 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ERCC6 | GRCh38.p7 | 10:49462123 | CAAAGTAACACCCTA[C/T]TGGACAATAAAACAC | 2074 |
rs144199158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530489 | AGGAGCAACTGTATA[C/T]GTATGGATGTGTGTG | 2074 |
rs144222786 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | ERCC6, PGBD3 | GRCh38.p7 | 10:49524674 | CTCCTGTTTCTGAGG[A/G]ATCTGGGTACCAAAA | 2074 |
rs144245719 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481821 | TAAAAATGCCACCTG[C/T]GTCTCCTGCCCCACC | 2074 |
rs144312638 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484751 | ACTCAAAAGAGAAAA[A/G]TGTTTTTAAAAATAA | 2074 |
rs144328884 | snp | A/C/G | 3.29686e-05 | 0.00405998 | missense, synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470417 | TTTTGTTTTTGACTT[A/C/G]TGCTTATAAAAATTA | 2074 |
rs144405680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466239 | ATAAAAACAAATATT[G/T]AACTTTAGTTAGTAT | 2074 |
rs144406144 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471642 | CCTGTCCCTCCCTGT[C/T]ATTTATTCTCCCAGC | 2074 |
rs144445150 | snp | A/G | 4.94271e-05 | 0.00497102 | stop-gained | ERCC6 | GRCh38.p7 | 10:49470701 | TCAAAGGATCACTTC[A/G]ATTAGAAGTTACTGC | 2074 |
rs144473543 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ERCC6 | GRCh38.p7 | 10:49476763 | TTGGACGGCAACCCT[C/T]ACCCTCCCAGCCCAC | 2074 |
rs144478015 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ERCC6 | GRCh38.p7 | 10:49475625 | TAGCTAGGAACTTCT[A/G]AATTCTGGACACTAG | 2074 |
rs144540948 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49527887 | ACAATGACTGCAAAG[A/G]TAATTTAGTTCCAGA | 2074 |
rs144548542 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ERCC6 | GRCh38.p7 | 10:49529761 | TGTAAGCACAAGTTG[A/G]GATGGCAGAACTGAA | 2074 |
rs144548889 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49478396 | GCTCATCTTGACATC[C/T]GACTTCATTCTCCGC | 2074 |
rs144580951 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481015 | TTAATGTTAAACTTC[A/G]TTCTGATTTTGTTGC | 2074 |
rs144584855 | snp | A/T | 3.29685e-05 | 0.00405995 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515952 | TTCTTTAAAGCTACA[A/T]CTGATTCCAGTGGAA | 2074 |
rs144600112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49499419 | GTTTATGGTTCATAT[C/T]TGGCTCTCTACTAAG | 2074 |
rs144608959 | snp | A/C | 0.000593648 | 0.0172183 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49493177 | GAACGGAGGCCACCA[A/C]GTGTGAAATTCCTTC | 2074 |
rs144680222 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ERCC6 | GRCh38.p7 | 10:49491410 | TGCTGTTTTTCCTCA[A/G]AAGTTAATTAAGAAT | 2074 |
rs144754885 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49515369 | GGAACACTTCACATG[C/T]AAGGCAACATCACAT | 2074 |
rs144779918 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49538580 | CTCTTATCAATTTGA[C/T]TCTATCAACGCCCAA | 2074 |
rs144860762 | snp | A/G | 6.59141e-05 | 0.00574045 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516737 | TGGTGCTGTAACTCT[A/G]CCTGCTACGGGTTGT | 2074 |
rs144865089 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ERCC6 | GRCh38.p7 | 10:49509250 | AACCTAGATTAGGAA[G/T]TGCTTAATAAACTAC | 2074 |
rs144882377 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468904 | GACAAAGGAGCCAGC[C/T]TGAAGGAGCTCCCAC | 2074 |
rs144913450 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493003 | ATTAACTTTAAATGC[A/G]GGAAAAAAAACACAG | 2074 |
rs144975232 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522891 | CATTACTACATAAGG[C/T]GCTACTAGAATGTGA | 2074 |
rs145034896 | snp | G/T | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49518181 | AATGGAGACAGGCTG[G/T]GAGGTTGGTGGTTCT | 2074 |
rs145066095 | in-del | -/ATA | 0.0107246 | 0.0724382 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533618 | ACCAGCCTGGGAAAG[-/ATA]ATGAGACCTTGTCTC | 2074 |
rs145132796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49511164 | GCCTGGTTTCTGCAC[A/G]CCAGCTGATGGAAAG | 2074 |
rs145177416 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519101 | TATCCTCATCCAAAT[G/T]CCCAGATTACAGGCT | 2074 |
rs145226862 | snp | C/T | 1.65094e-05 | 0.00287305 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515995 | GATCCTTTCTCACTG[C/T]ACCTGTTGCCTGATG | 2074 |
rs145235527 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49522667 | ATTGACCCAATTTAA[C/T]TGGAAAAATATATAT | 2074 |
rs145272065 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468435 | AGTTCATTTGTTTCC[C/T]ATCTCTCAAGAGATC | 2074 |
rs145272593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49521460 | AATGTGCAAAGCAGT[A/G]GTATATTTTAAGAAA | 2074 |
rs145281709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49471775 | GGCCCAGCATGTGGT[A/G]AAGGGCACAGAGCTT | 2074 |
rs145326258 | snp | A/C/T | 4.94281e-05 | 0.00497112 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515635 | AAGCATTTTGTAAGA[A/C/T]CAGTTCGAAACAGAA | 2074 |
rs145353612 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49454678 | TAAAAGATATTTCAA[C/T]GTTAGAAAATTTAAC | 2074 |
rs145407497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49528005 | AGATGTCTTTTCTTA[A/G]ACTGATGCTTGGAAA | 2074 |
rs145461918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49493859 | TGCTCCTCTACACCA[C/G]CAAAGCACCATGGAG | 2074 |
rs145468454 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | ERCC6 | GRCh38.p7 | 10:49537814 | TGCAACCTCCGCCTT[A/C]CGGGTTCAAGCGATT | 2074 |
rs145544509 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | ERCC6 | GRCh38.p7 | 10:49536335 | CAAGAAAAACTAGAG[A/C]ACGTAATGGCTGGAG | 2074 |
rs145554525 | snp | C/T | 6.58957e-05 | 0.00573964 | missense | ERCC6 | GRCh38.p7 | 10:49458897 | TTTCTCAATAGTTCT[C/T]GGAAGACACAAGACT | 2074 |
rs145612441 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | ERCC6 | GRCh38.p7 | 10:49540061 | TTTTGTTTTTGAGAC[A/G]GAGTTTTGCTCTTGT | 2074 |
rs145622432 | snp | C/T | 0.000280036 | 0.0118296 | missense | ERCC6 | GRCh38.p7 | 10:49459081 | GCCCGCTTTCACTTT[C/T]TAAACGCTCTGGCAG | 2074 |
rs145634791 | snp | C/T | 4.94181e-05 | 0.00497057 | intron-variant | ERCC6 | GRCh38.p7 | 10:49478331 | GCTTTAGGAATGCTT[C/T]GTTAACTCCTGGATT | 2074 |
rs145668431 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49468038 | ATACCCAATGCCCCA[A/T]GAAATATTTTTCCAG | 2074 |
rs145720191 | snp | A/C/T | 0.00237304 | 0.0343645 | missense | ERCC6 | GRCh38.p7 | 10:49472376 | ACTGTGTGCACTGAC[A/C/T]GGTGGTAGATCTTTT | 2074 |
rs145751821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49477981 | CTTTTTGTGACACTC[C/T]CCCTCAAGAATAAAT | 2074 |
rs145803359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49519535 | CCACTTCAGGCTATG[C/G]ATTTAGCAGCTTAGC | 2074 |
rs145822221 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ERCC6 | GRCh38.p7 | 10:49531343 | ACTAAACTTTGTGGT[A/G]CAAAGAAAACAAATC | 2074 |
rs145823189 | snp | A/C/T | 8.23887e-05 | 0.00641785 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49482795 | GATGAAGTCAAAGAG[A/C/T]GACCACAGCTCTCGG | 2074 |
rs145826323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49497660 | CTCCATTAACAGTCA[C/T]ATCGTCAACTGAACC | 2074 |
rs145854593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481936 | CCTCCCTCTTGTGAC[C/T]ACCCTGTAGCCTGAG | 2074 |
rs145869154 | snp | C/G | | | intron-variant | ERCC6, PGBD3 | GRCh38.p7 | 10:49523758 | CACACTCAGCCCTCT[C/G]TATGCCTCTTGCCCC | 2074 |
rs145917244 | snp | A/G | 0.000346018 | 0.0131487 | synonymous-codon, utr-variant-5-prime | ERCC6, PGBD3 | GRCh38.p7 | 10:49524200 | CTTCTGCCGTTTCCC[A/G]CCCTTGGGCAGAGGC | 2074 |
rs146001450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484341 | ACCATAAATGGAGCC[A/G]AGATTTGAATCTACA | 2074 |
rs146020207 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ERCC6 | GRCh38.p7 | 10:49489662 | AACTACTAGAGACTA[C/T]GTAGCAAAAAAAGGT | 2074 |
rs146043988 | snp | C/G | 0.00192617 | 0.0309738 | missense | ERCC6 | GRCh38.p7 | 10:49474235 | AGGGCTATAAGTCCG[C/G]AGAAAATCTGTGGTA | 2074 |
rs146087611 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ERCC6 | GRCh38.p7 | 10:49484852 | TACCTGCATCAGACA[C/T]CTTTTCTGCAACACT | 2074 |
rs146106620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49490431 | ACAGTCCAGGCTCAC[C/T]GCAACCTCCGCCTCT | 2074 |
rs146165518 | snp | A/G | 0.000148323 | 0.00861042 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532581 | ATACTCCTTCTCCAC[A/G]TCAACGAGCTGGGAG | 2074 |
rs146219430 | snp | A/G | 3.29592e-05 | 0.00405938 | missense | ERCC6 | GRCh38.p7 | 10:49528479 | GCTCCTCCAAGGATG[A/G]CCTGGAGATGCTTTT | 2074 |
rs146226805 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ERCC6 | GRCh38.p7 | 10:49513157 | TCACCCATGAAGAAG[A/G]TACTGCTGTGATCCC | 2074 |
rs146326941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49530304 | AACTTTGTGATGGGT[C/T]TATCAGGGCATAACC | 2074 |
rs146345399 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49533561 | GCCAAAGCGGGAGGA[C/T]AGAGACCAGCCAGGG | 2074 |
rs146366617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49466856 | CAATGGTGTGATCTC[A/G]GCTCACTGCAACCTC | 2074 |
rs146371365 | snp | C/T | 0.00016472 | 0.00907375 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49532719 | GGCGCTAGGCTCTAC[C/T]GCCTGGATCTGATGT | 2074 |
rs146441160 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, missense | ERCC6, PGBD3 | GRCh38.p7 | 10:49515863 | AGGCAACAGTGACAA[C/T]ACTGTTATCATTCCA | 2074 |
rs146492193 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ERCC6 | GRCh38.p7 | 10:49508142 | TAACATAAACCTTGG[A/G]AGAATCACAGCCACT | 2074 |
rs146493285 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon | ERCC6 | GRCh38.p7 | 10:49470318 | TCCTTCAAACTTGGC[A/G]TCTCTGCAATGCTTA | 2074 |
rs146529081 | snp | A/G | 0.00874735 | 0.0655527 | utr-variant-3-prime | ERCC6 | GRCh38.p7 | 10:49455869 | ACAAAACAACCTATC[A/G]ATATTGATACCACTT | 2074 |
rs146540023 | snp | A/C/G | 3.30045e-05 | 0.00406219 | missense | ERCC6 | GRCh38.p7 | 10:49470473 | AAGCTTCTGTTTGAG[A/C/G]CTGGCTGGGTCTTTC | 2074 |
rs146553674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ERCC6 | GRCh38.p7 | 10:49481872 | CAAGATCAGGTCCAG[A/G]TCCTCATGGCCCTCA | 2074 |
rs146613178 | snp | C/T | 0.000197703 | 0.00994045 | intron-variant, synonymous-codon | ERCC6, PGBD3 | GRCh38.p7 | 10:49516836 | TTGCTGCACAGTAAA[C/T]GTAGATGGAACTTCA | 2074 |