SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs489922 | snp | A/C | 0.482757 | 0.0912364 | intron-variant | VCP | GRCh38.p7 | 9:35069611 | GCATGCGCCACCACA[A/C]CTGGCTAATTTTGCA | 7415 |
rs495417 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35070207 | GCTTCCCCCATTCCA[A/C]AAGTCTGCCACTCCA | 7415 |
rs514492 | snp | C/T | 0.380752 | 0.213082 | intron-variant | VCP | GRCh38.p7 | 9:35062975 | ATGAACCAAATATCT[C/T]ACCATTGATCAAGAA | 7415 |
rs562381 | snp | A/G | 0.426354 | 0.177198 | intron-variant | VCP | GRCh38.p7 | 9:35060749 | CCTGAGATCACCCAG[A/G]TCAATTACAATGTAC | 7415 |
rs595429 | snp | C/T | 0.498369 | 0.0285077 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055672 | ccctattttatcgtg[C/T]agtggcctatgaaac | 7415 |
rs607671 | snp | A/G | 0.469839 | 0.119042 | intron-variant | VCP | GRCh38.p7 | 9:35062616 | CCTCTGGCTAGAGCA[A/G]GAGAGATGGCACACC | 7415 |
rs622945 | snp | A/G | 0.483563 | 0.0891524 | intron-variant | VCP | GRCh38.p7 | 9:35063727 | CTACACTCTAGACCA[A/G]TAGTTCTCAAATGTT | 7415 |
rs623318 | snp | G/T | 0.151001 | 0.229563 | intron-variant | VCP | GRCh38.p7 | 9:35063792 | CCTTAACTTCCTTAC[G/T]TCTACTGGGTGACAT | 7415 |
rs637885 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | VCP | GRCh38.p7 | 9:35064791 | GCATTAGGTAAATCC[A/G]AGAAACAATTAGGCC | 7415 |
rs684562 | snp | C/T | 0.485051 | 0.0851533 | intron-variant | VCP | GRCh38.p7 | 9:35060305 | TAGTTCAGCCTATTG[C/T]AGCTCACCTTGTCAA | 7415 |
rs739844 | snp | C/G | 0.482757 | 0.0912364 | intron-variant | VCP | GRCh38.p7 | 9:35072004 | GGCCCACTccgccgg[C/G]gcggcgccccggggc | 7415 |
rs1053318 | snp | G/T | 0.303688 | 0.244167 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056964 | TGACTCTGGACAGGG[G/T]GTTTCTGTTGCAAAA | 7415 |
rs1053424 | snp | C/T | 0 | 0 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056773 | GCCACAGTAAAGCAT[C/T]TGCACTTGACTCAAT | 7415 |
rs1053442 | snp | A/C | 0 | 0 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056704 | AGGTGGGTAGGGGCC[A/C]CAGTTGCTGGATGTT | 7415 |
rs1053447 | snp | A/G/T | 0 | 0 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056682 | CTGGATGTTTATATA[A/G/T]AGAGTAGGTTGATTT | 7415 |
rs1053453 | snp | C/T | 0 | 0 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056617 | AATCACAAGCAGTTT[C/T]TAAACCAAAAAATGA | 7415 |
rs1984059 | snp | A/G | 0.306182 | 0.243605 | intron-variant | VCP | GRCh38.p7 | 9:35058590 | ACGTGGTGAAACCAC[A/G]TTTCTACTAAAAAAA | 7415 |
rs1984060 | snp | C/G | 0.305934 | 0.243663 | intron-variant | VCP | GRCh38.p7 | 9:35058611 | ACTAAAAAAAAAATA[C/G]AAAAAACTAGCCGGA | 7415 |
rs1984061 | snp | A/G | 0.306182 | 0.243605 | intron-variant | VCP | GRCh38.p7 | 9:35058664 | CCCAGCTACTCGGGA[A/G]GCTGAGGCAGGAGAA | 7415 |
rs2073575 | snp | A/T | 0.215446 | 0.2476 | intron-variant | VCP | GRCh38.p7 | 9:35068643 | AATGGCCTAAGAAGA[A/T]GACATAATAGAAATG | 7415 |
rs2073576 | snp | C/T | 0.15665 | 0.231917 | intron-variant | VCP | GRCh38.p7 | 9:35068951 | ATTAACAGTATAGAG[C/T]AAAGCATAAGCTAAC | 7415 |
rs2074549 | snp | C/T | 0.216048 | 0.247684 | intron-variant | VCP | GRCh38.p7 | 9:35061506 | CACATCTTAACCTTA[C/T]GTCTCTAGCCAGTTC | 7415 |
rs2237856 | snp | C/G | 0.0941369 | 0.195465 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074683 | CTACTCCTGTGCAAC[C/G]CACAACAGCAGAGTC | 7415 |
rs2258240 | snp | C/T | 0.378888 | 0.214215 | intron-variant | VCP | GRCh38.p7 | 9:35060958 | TGGGGATGAGACTTA[C/T]CAAGGGAGGGGTCAA | 7415 |
rs2299612 | snp | C/T | 0.2776 | 0.248472 | intron-variant | VCP | GRCh38.p7 | 9:35070729 | GCCTGAGCCACTGTG[C/T]CCGGTCAATAGTTTG | 7415 |
rs2299613 | snp | C/T | 0.298398 | 0.245271 | intron-variant | VCP | GRCh38.p7 | 9:35071094 | AGGTTCCAAGAATTT[C/T]AGATTTTTACTTTTG | 7415 |
rs3178209 | snp | C/T | 0 | 0 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057000 | GCTCCATTCTCCAGT[C/T]TGAACAGTTCAGCTA | 7415 |
rs3193957 | snp | A/C | 0 | 0 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056785 | CTACTGCCACCTGCC[A/C]CAGTAAAGCATCTGC | 7415 |
rs3955024 | snp | C/G | | | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072715 | TCGCCCGCCTCTCCG[C/G]GCCTCTCCCCAGCAA | 7415 |
rs6150985 | in-del | -/AT/G/GTACACAAACA | 0.000264502 | 0.011497 | intron-variant | VCP | GRCh38.p7 | 9:35061710 | GACAGTACACAAACA[-/AT/G/GTACACAAACA]TAAACAGGGCTCATC | 7415 |
rs7871544 | snp | A/C | 0.215446 | 0.2476 | intron-variant | VCP | GRCh38.p7 | 9:35071777 | GCCCCGCCGACCCGG[A/C]TCCAAAAAGGCGGCT | 7415 |
rs7871782 | snp | A/G | 0.215446 | 0.2476 | intron-variant | VCP | GRCh38.p7 | 9:35071776 | GGCCCCGCCGACCCG[A/G]CTCCAAAAAGGCGGC | 7415 |
rs9696500 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066595 | tttaaaaaaaaaaaa[A/G]gaaaaagaaaatgag | 7415 |
rs10118503 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | VCP | GRCh38.p7 | 9:35071075 | AGAAACAGCTGATGA[C/T]GCCAGGTTCCAAGAA | 7415 |
rs10972300 | snp | C/T | 0.300936 | 0.244756 | intron-variant | VCP | GRCh38.p7 | 9:35068204 | AACCTGGGAAAATCC[C/T]TCAAGTAAGTGCAGT | 7415 |
rs11272867 | in-del | -/ACAGTACACAA | 0.487061 | 0.0795001 | intron-variant | VCP | GRCh38.p7 | 9:35061696 | AAAGCGACCTGTGGG[-/ACAGTACACAA]ACAGTACACAAACAT | 7415 |
rs11546022 | snp | C/T | 0 | 0 | missense | VCP | GRCh38.p7 | 9:35057505 | AGGATGATCCAGTGC[C/T]TGAGATCCGTCGAGA | 7415 |
rs11546023 | snp | C/T | | | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072393 | CTCGTAGCCGTTACC[C/T]GCGGGCCGCCACAGC | 7415 |
rs11546024 | snp | A/T | | | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072562 | GCCGCTGCCACTGCC[A/T]CTGCCACCTCGCGGA | 7415 |
rs11546026 | snp | A/C | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056256 | AATGGCACCCCAACA[A/C]AGTCTTTGGTCAGGA | 7415 |
rs12001493 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35069180 | ACAGACATCAAACCG[C/G]CAGAAAGAGGCTCAA | 7415 |
rs12004343 | snp | C/T | 0 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35060691 | AAGAACAGTAGGTTC[C/T]TAAGTCGTGCTCTCA | 7415 |
rs12337915 | snp | C/G | 0.0707826 | 0.174302 | intron-variant | VCP | GRCh38.p7 | 9:35066159 | aaTGAgactaggctt[C/G]atggctcatgcctgt | 7415 |
rs12349922 | snp | A/C | 0.00356863 | 0.0420901 | intron-variant | VCP | GRCh38.p7 | 9:35061698 | AAGCGACCTGTGGGA[A/C]AGTACACAAACATAA | 7415 |
rs12376181 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066057 | cttgaacccaggagg[C/T]ggaggttgcagtgag | 7415 |
rs12376182 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066082 | agtgagccgagattg[C/G]accactgcgctccag | 7415 |
rs12376198 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066075 | aggttgcagtgagcc[A/G]agattgcaccactgc | 7415 |
rs12553165 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VCP | GRCh38.p7 | 9:35058767 | gtgagacttcgtctc[A/C]aaaaaaaaacaaaaa | 7415 |
rs12553166 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35058771 | gacttcgtctcaaaa[A/C]aaaaacaaaaaacaa | 7415 |
rs12553167 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35058778 | tctcaaaaaaaaaac[A/C]aaaaacaaaaaacaa | 7415 |
rs12555735 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35058777 | gtctcaaaaaaaaaa[A/C]aaaaaacaaaaaaca | 7415 |
rs12555737 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35058784 | aaaaaaaacaaaaaa[A/C]aaaaaacaaaaaAAA | 7415 |
rs12686362 | snp | A/G | 0.306431 | 0.243548 | intron-variant | VCP | GRCh38.p7 | 9:35057771 | GGCTTAAGGAGGGGA[A/G]ATGTTGACTGAAGTG | 7415 |
rs16932168 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | VCP | GRCh38.p7 | 9:35058842 | CTTTGATTTCCCTCA[C/T]GGAGCTTGGTTCAGA | 7415 |
rs16932174 | snp | C/G | 0.000164715 | 0.0090736 | intron-variant | VCP | GRCh38.p7 | 9:35062965 | TAGACATAAGATGAA[C/G]CAAATATCTCACCAT | 7415 |
rs17878564 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073857 | TCCTTTTCTGTTGTC[A/G]AGTAAAATTTCATAT | 7415 |
rs17878854 | snp | C/T | 0.000296545 | 0.0121731 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074169 | GCTGGATCCGTCCCT[C/T]TGATCGTGACGCCTT | 7415 |
rs17879075 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074704 | ATCCTCAGACACAAA[A/G]ACCATGACTCTGCTG | 7415 |
rs17882628 | snp | A/G | 0.00795532 | 0.062565 | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073159 | GTGACAATGGGGTAG[A/G]AGTGGGGTGCTAGTC | 7415 |
rs17883025 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074723 | GTTCCCTGGTTTCCC[C/T]GATATCCTCAGACAC | 7415 |
rs17885597 | snp | A/G | 0.0143877 | 0.0835874 | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073332 | TTTTCTTGCTAATTT[A/G]GGTTCTACTGAATTG | 7415 |
rs17886096 | snp | A/G | 0.00795532 | 0.062565 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073650 | ATTGCCTGAATGCAG[A/G]GCCCCAAAGCCCAGG | 7415 |
rs28391478 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | VCP | GRCh38.p7 | 9:35058458 | CCATCAGGGATAAGT[A/C]TATGAGTCTCATCTC | 7415 |
rs28589520 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35058654 | TGCCTGTAGTCCCAG[A/C]TACTCGGGAGGCTGA | 7415 |
rs34097935 | snp | C/T | 0.00135077 | 0.0259531 | synonymous-codon | VCP | GRCh38.p7 | 9:35062235 | TGAGCTAGATGCCAT[C/T]GCTCCCAAAAGAGAG | 7415 |
rs34301260 | in-del | -/T | 0.439502 | 0.163061 | intron-variant | VCP | GRCh38.p7 | 9:35066265 | GTGAGACCCTGTCTC[-/T]TTTTTTTTTTTTTTG | 7415 |
rs34556626 | in-del | -/G | | | intron-variant | VCP | GRCh38.p7 | 9:35064413 | TTCTCAACCCGGCAT[-/G]GGTGGCTCACATCTG | 7415 |
rs34716226 | in-del | -/C | 0.285275 | 0.247499 | intron-variant | VCP | GRCh38.p7 | 9:35058770 | GACTTCGTCTCAAAA[-/C]AAAAAACAAAAAACA | 7415 |
rs34820387 | in-del | -/G | | | intron-variant | VCP | GRCh38.p7 | 9:35064974 | TGGGTTCAACCGATT[-/G]CTCCTGCCTCAGCCT | 7415 |
rs35042918 | in-del | -/AA | 0.345037 | 0.231231 | intron-variant | VCP | GRCh38.p7 | 9:35060131 | GCCAGACCCTGTCTC[-/AA]GAGAGAGAGAGAGAA | 7415 |
rs35057847 | in-del | -/C | | | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074025 | AGGAATGGTCACATT[-/C]CTAATGATGGTGAAG | 7415 |
rs35269655 | in-del | -/A | 0.444931 | 0.15653 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35056038 | TGGAAAAAAAAAAAA[-/A]TTCAATACTAAAATT | 7415 |
rs35498216 | in-del | -/T | | | intron-variant | VCP | GRCh38.p7 | 9:35069469 | CAAGCTCCCTCTCCC[-/T]TTTTTTTTTTTTTTT | 7415 |
rs35504855 | in-del | -/A | 0.471483 | 0.115954 | intron-variant | VCP | GRCh38.p7 | 9:35066582 | TTAAAAAAAAAAAAA[-/A]GAAAAAGAAAATGAG | 7415 |
rs35523363 | in-del | -/C | | | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055704 | TCTGTTGTGTTGTTT[-/C]CTCAAATAAATACGC | 7415 |
rs36090068 | in-del | -/C | | | splice-donor-variant | VCP | GRCh38.p7 | 9:35059491 | ATGATCTTGCACCTG[-/C]CCTTGGCAACTGGGG | 7415 |
rs41274873 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VCP | GRCh38.p7 | 9:35065521 | ACCTCTCCCCAACTC[C/T]ACCCCACCTGTCTTA | 7415 |
rs41274875 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073818 | CCTTCCCACGCAAGT[A/G]TATGTAGTAGGCAGA | 7415 |
rs45453195 | snp | C/T | | | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074695 | CACAAAGACCATGAC[C/T]CTGCTGTTGTGGGTT | 7415 |
rs45537335 | snp | C/T | 0.000913856 | 0.0213563 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074493 | GGCTGGGGCTACAGG[C/T]AATCGAGACACTTAC | 7415 |
rs55745923 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056521 | GGGTAGCCCAAGGCT[A/G]TTCCCAGGAAAAGAA | 7415 |
rs56217414 | in-del | -/AG | 0.00392416 | 0.0441212 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074519 | CCCAGCCCAGAGTAC[-/AG]AGTCTTAGAACTTGA | 7415 |
rs56405035 | snp | C/T | 3.30797e-05 | 0.00406679 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074069 | CCACAGAGAGACAGC[C/T]CACTGGGGACCCAGC | 7415 |
rs56406106 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074693 | GCAACCCACAACAGC[-/AG]AGTCATGGTCTTTGT | 7415 |
rs56793340 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | VCP | GRCh38.p7 | 9:35058381 | TTACCTTTATGGAAC[G/T]TACAAACACATGAAT | 7415 |
rs57478775 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35058791 | ACAAAAAACAAAAAA[A/C]AAAAAAAACCTTGCT | 7415 |
rs60834503 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | VCP | GRCh38.p7 | 9:35060103 | ACCACTGCCCTCCAA[C/T]CTGGGCAACAGAGCC | 7415 |
rs61752947 | snp | A/G | 0.00383222 | 0.0436053 | synonymous-codon | VCP | GRCh38.p7 | 9:35061679 | AATATCTACCTCCCT[A/G]TCAAAGCGACCTGTG | 7415 |
rs62544156 | snp | A/G | 0.002198 | 0.0330782 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057105 | AGCTCACTGCACGCT[A/G]GCCACCACCACTTAG | 7415 |
rs72722960 | snp | A/G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35060131 | GCCAGACCCTGTCTC[A/G/T]AGAGAGAGAGAGAGA | 7415 |
rs73645450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058949 | GATGCCCTATTAAAA[C/T]TCTTCTCAGTTAGAT | 7415 |
rs74763589 | snp | A/C | 0.145978 | 0.227331 | intron-variant | VCP | GRCh38.p7 | 9:35061493 | AAACCCATCTCCTCA[A/C]ATCTTAACCTTATGT | 7415 |
rs74989038 | snp | C/T | 0.00557542 | 0.0525036 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055715 | TGTTTCTCAAATAAA[C/T]ACGCTTTTAAAAATG | 7415 |
rs75294761 | snp | G/T | 0 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35071292 | TCCTTGGGCTGGCTG[G/T]GTTTTTTTTTTTTTT | 7415 |
rs75784354 | snp | C/T | 0.5 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35069493 | GTTTCGCTTTTGTTG[C/T]CCAGGCTGGAATGCA | 7415 |
rs75819288 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | VCP | GRCh38.p7 | 9:35060147 | AGAGAGAGAGAGAGA[A/G]AAAAAAAATAACACT | 7415 |
rs75869957 | snp | G/T | 0 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35069464 | TTTTTTTTTTTTTTT[G/T]TTTTTGAGATGGAGT | 7415 |
rs75942852 | snp | A/G | 0.5 | 0 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35056037 | GTCTATTTTCTGTTT[A/G]GAAAAAAAAAAAATT | 7415 |
rs76189776 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | VCP | GRCh38.p7 | 9:35071427 | AGCCCCAGAGCCCGG[G/T]TAATTTCTCAATATA | 7415 |
rs76360394 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056211 | CACCTGCAAGTAAGA[C/T]TGTATTCTTTTGCAA | 7415 |
rs76493366 | snp | G/T | 0.5 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35071323 | TTTTTTTTTTTTTTT[G/T]CCTCTAAAAGCTCTC | 7415 |
rs77126390 | snp | A/C | 0.00292791 | 0.0381495 | intron-variant | VCP | GRCh38.p7 | 9:35060753 | AGATCACCCAGATCA[A/C]TTACAATGTACTGAG | 7415 |
rs77203288 | snp | G/T | 0.5 | 0 | synonymous-codon | VCP | GRCh38.p7 | 9:35059658 | GAACACATTTTTTTT[G/T]GTGGACATGCCATCC | 7415 |
rs77248841 | snp | C/T | | | missense | VCP | GRCh38.p7 | 9:35060438 | TGGCCAACAAAGTTT[C/T]CCCACAGCCAGGAGG | 7415 |
rs77294357 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | VCP | GRCh38.p7 | 9:35057998 | ATTACATCCTACCTA[A/G]CGGTCTCACTTCCAG | 7415 |
rs77619779 | snp | A/C | 0.0689305 | 0.172377 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055570 | TTGACCTATTTCTTT[A/C]TGAATGTTTCATCTG | 7415 |
rs77654833 | snp | A/G | 0.5 | 0 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35056039 | CTATTTTCTGTTTGG[A/G]AAAAAAAAAAATTCA | 7415 |
rs78337044 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | VCP | GRCh38.p7 | 9:35067693 | CTCAAGGGACCTGCA[A/G]AAATGGATTTTGAAG | 7415 |
rs78602605 | snp | C/G/T | 1.64803e-05 | 0.00287052 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074330 | AGGACTCTAGGACAC[C/G/T]AACTGCCCCTCAGCC | 7415 |
rs78639645 | snp | C/T | 0.0148787 | 0.0849585 | intron-variant | VCP | GRCh38.p7 | 9:35068216 | TCCCTCAAGTAAGTG[C/T]AGTAAGGAAAGACTA | 7415 |
rs111331448 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | VCP | GRCh38.p7 | 9:35071195 | CTGAGTAATACTTTA[C/T]CCGAATTCAGAAACT | 7415 |
rs111335122 | snp | A/G | 0.5 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35060626 | CATGGTGTACCCAAT[A/G]GTATCAGATCCAGGT | 7415 |
rs111340417 | snp | C/T | 0.5 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35062603 | AAATGCTCTAGGACC[C/T]CTGGCTAGAGCAAGA | 7415 |
rs111903589 | snp | C/T | 0.5 | 0 | missense | VCP | GRCh38.p7 | 9:35057142 | AGGTCATCATCATTG[C/T]CTTCTGTGTATACAC | 7415 |
rs111903864 | snp | C/G/T | 0 | 0 | splice-donor-variant | VCP | GRCh38.p7 | 9:35062216 | TCAGGTAAGCTCCTA[C/G/T]TTTCTCTCTTTTGGG | 7415 |
rs111924414 | snp | A/G | 0.5 | 0 | synonymous-codon | VCP | GRCh38.p7 | 9:35057441 | ATACTTCCGAATGTC[A/G]TTGTCACTGACAGAA | 7415 |
rs111980191 | snp | A/C | 0.5 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35067235 | TAAGCACTCCCAAGA[A/C]GAAAGCTACATGAAA | 7415 |
rs111991598 | snp | C/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056075 | AAAATTTTATATTAA[C/T]AAAAAGTTTTTTTTT | 7415 |
rs112293411 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | VCP | GRCh38.p7 | 9:35070084 | AGAAAAACAAACCCC[A/G]TTCATCTAACAAAAT | 7415 |
rs112366806 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | VCP | GRCh38.p7 | 9:35063940 | GTTTTGTGCGCACAC[A/G]CACACAACAGACAAT | 7415 |
rs112517019 | snp | A/G | 0.5 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35071425 | AAAGCCCCAGAGCCC[A/G]GGTAATTTCTCAATA | 7415 |
rs112533775 | snp | A/G/T | 0 | 0 | splice-donor-variant | VCP | GRCh38.p7 | 9:35062215 | CTCAGGTAAGCTCCT[A/G/T]CTTTCTCTCTTTTGG | 7415 |
rs112720765 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | VCP | GRCh38.p7 | 9:35057750 | CAGAAATCACATCAG[C/T]GATGGGGCTTAAGGA | 7415 |
rs112820873 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | VCP | GRCh38.p7 | 9:35063704 | CCCACTAGGAAAAGA[C/T]TGAGAAGCTACACTC | 7415 |
rs112997283 | snp | G/T | 0.5 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35063775 | TAACACTCTGAAAAT[G/T]TCCTTAACTTCCTTA | 7415 |
rs113013966 | snp | A/G | 0.5 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35063667 | GTAACTTCATCTTCA[A/G]TGTGTTCCATGGAAA | 7415 |
rs113230475 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VCP | GRCh38.p7 | 9:35059927 | CACTTGAGGCCAGAA[A/G]TCCGAAACCAGCATG | 7415 |
rs113543353 | snp | A/G | 0.5 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35061324 | TACCTTTATGGGCTG[A/G]GTTTTAAGTACTTAA | 7415 |
rs113725156 | snp | C/G | 0.5 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35070546 | TCAAGTGATTCTCCT[C/G]TCTCAGCCTCCAGAG | 7415 |
rs113734714 | in-del | -/A | 0.0879971 | 0.190408 | intron-variant | VCP | GRCh38.p7 | 9:35066125 | GCGACACTCTGTCTC[-/A]AAAAAAAAAAGAAAA | 7415 |
rs113905995 | snp | C/G/T | 0 | 0 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056562 | GGCCCAGGACTCAGG[C/G/T]TCCATTTTGACCCAA | 7415 |
rs114256093 | snp | A/G | 0.00808919 | 0.0630806 | intron-variant | VCP | GRCh38.p7 | 9:35068367 | CACCTTTTGAACTAG[A/G]AGGAGGAAATGGAGT | 7415 |
rs114783706 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | VCP | GRCh38.p7 | 9:35064647 | AGTCTTACTGAGAAG[C/G]GGTCTCTAAAATCTG | 7415 |
rs116532976 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VCP | GRCh38.p7 | 9:35062881 | TAAACATGAAGGAGG[A/G]CATGGGTGCAAAAAG | 7415 |
rs116725733 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | VCP | GRCh38.p7 | 9:35067604 | TATCCTAAGCCAGGA[C/T]ATAAGTATGATAAAT | 7415 |
rs116985782 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35065451 | GAGAACTCATCAGAC[A/C]CTGGGGTCAAAATGC | 7415 |
rs118041972 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | VCP | GRCh38.p7 | 9:35068571 | CCTGGTATTTTGAGC[A/G]TCAGTGTCCCAGCTA | 7415 |
rs118166920 | snp | A/C | 0.0832709 | 0.186283 | intron-variant | VCP | GRCh38.p7 | 9:35060024 | ATAGTCCCAGCTACT[A/C]AGGAGGCTGAAGTAG | 7415 |
rs121909329 | snp | A/C/G | | | missense | VCP | GRCh38.p7 | 9:35065363 | ACATTTTTCTTGTCC[A/C/G]TGGTGGGATGCGTGC | 7415 |
rs121909330 | snp | C/T | | | missense | VCP | GRCh38.p7 | 9:35065364 | GACATTTTTCTTGTC[C/T]GTGGTGGGATGCGTG | 7415 |
rs121909331 | snp | A/C | | | missense | VCP | GRCh38.p7 | 9:35064167 | CTGCCCTCTTTAAGG[A/C]AATTGGTGTGAAGGT | 7415 |
rs121909332 | snp | C/G/T | | | missense | VCP | GRCh38.p7 | 9:35067910 | AATAACCTTCGTGTA[C/G/T]GCCTAGGGGATGTCA | 7415 |
rs121909334 | snp | A/G | | | missense | VCP | GRCh38.p7 | 9:35065255 | GGGAGCCTATCAAAC[A/G]AGAGGTGAGTTTTCT | 7415 |
rs121909335 | snp | A/G | | | missense | VCP | GRCh38.p7 | 9:35065351 | TCCGTGGTGGGATGC[A/G]TGCTGTGGAGTTCAA | 7415 |
rs137953487 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056679 | AATAAATCAACCTAC[C/T]CTCTATATAAACATC | 7415 |
rs138168961 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35070602 | TCACCATGCCTGGCT[A/G]CTTTTTGCATTTTAA | 7415 |
rs138320082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35064577 | CTCAAAGAACAACTA[C/T]AAAAATCCCAAGGCA | 7415 |
rs138403227 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35063897 | TTCTAAGAGTTGTAA[A/G]GAAAAACCCATATAT | 7415 |
rs138404848 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35069995 | CCTCACAATTTGCAA[A/G]AGACAAAGAAAAATG | 7415 |
rs138450723 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35060599 | TAAACAGAAGCATCC[C/T]CTCCATTATTTCATG | 7415 |
rs138760141 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VCP | GRCh38.p7 | 9:35064388 | GTGCAAAAACCTACC[A/G]TATAAGAAGATTCTC | 7415 |
rs138855718 | snp | C/G | 0.000330562 | 0.0128519 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074442 | AGTGGCCTCATCCCT[C/G]CGATCTAGCCTCTTC | 7415 |
rs138919510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060220 | GCAGTTGAGCAGCCA[A/G]CACTAAGAATATTTC | 7415 |
rs139020111 | snp | G/T | | | downstream-variant-500B | VCP | GRCh38.p7 | 9:35056036 | AGTCTATTTTCTGTT[G/T]GGAAAAAAAAAAAAT | 7415 |
rs139130688 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | VCP | GRCh38.p7 | 9:35068048 | CTCGGAACAACTGCA[A/G]TTCATCCATCTTGGG | 7415 |
rs139225387 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35071366 | AATGGGCTGAGGTAG[C/G]CAAGTTTTATCTAAC | 7415 |
rs139510624 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | VCP | GRCh38.p7 | 9:35066977 | GGTGGAAGTGAGGGC[A/G]AAGGAACAGCCCCAC | 7415 |
rs139578612 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VCP | GRCh38.p7 | 9:35058410 | ATTTGCCTTTTCATT[C/T]TGGGAGGTCTGTGGA | 7415 |
rs139697962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35062362 | GGACCTGAAAGGATA[C/T]AGAATGGAGACAATA | 7415 |
rs139707968 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VCP | GRCh38.p7 | 9:35058887 | TGACCATCTCTTCTC[A/G]GCCTTATTCCAAATT | 7415 |
rs139789152 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VCP | GRCh38.p7 | 9:35065888 | GAAAATGAGTCTAGC[A/G]GCCGGGCACAGTGGC | 7415 |
rs139938566 | in-del | -/AAAAAC/AAC | | | intron-variant | VCP | GRCh38.p7 | 9:35060253 | CCTCTTAAAGAAAAA[-/AAAAAC/AAC]CAGCCTCTATTCCTT | 7415 |
rs139980401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071463 | TTGGGGAAAGGAGTG[A/C]GCGCACGTTTGTGTT | 7415 |
rs140485754 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VCP | GRCh38.p7 | 9:35069800 | AAGGCTCAGGAAAAC[A/G]TAAGCATTAACCAAA | 7415 |
rs140635919 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VCP | GRCh38.p7 | 9:35059272 | CTCCTCTCGAGATAC[A/G]CAGATCTTTGGGCTA | 7415 |
rs140669606 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35059916 | GGTGGGAGGATCACT[C/T]GAGGCCAGAAATCCG | 7415 |
rs140715692 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VCP | GRCh38.p7 | 9:35063205 | TAAGAATAAGCCCTC[C/T]GCAGTAAATGCTAAG | 7415 |
rs140722219 | snp | C/T | 5.23291e-05 | 0.00511486 | intron-variant | VCP | GRCh38.p7 | 9:35060272 | CCTCTATTCCTTGCC[C/T]TCAGGCAAATCAATA | 7415 |
rs140913250 | snp | C/T | 0.00107016 | 0.023107 | missense | VCP | GRCh38.p7 | 9:35068301 | TGGCTTCATCAACAA[C/T]TAACCGATTGGGACG | 7415 |
rs141223575 | snp | A/G/T | 0.000687574 | 0.018529 | intron-variant | VCP | GRCh38.p7 | 9:35059459 | AGCCTGAGGACTCAT[A/G/T]CAAGTCTCCCACAGC | 7415 |
rs141235266 | snp | C/T | 0.00953873 | 0.0683987 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055944 | TAGTAATTTATTTTC[C/T]CTGCACTACTCTCTC | 7415 |
rs141275388 | snp | G/T | 1.64749e-05 | 0.00287005 | synonymous-codon | VCP | GRCh38.p7 | 9:35059601 | GCCAGGTCTGAGGAT[G/T]GCAGGATCAATGATG | 7415 |
rs141332754 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35063916 | AAACCCATATATATA[C/T]GTGTGTGTGTTTTGT | 7415 |
rs141400885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35061325 | ACCTTTATGGGCTGG[A/G]TTTTAAGTACTTAAT | 7415 |
rs141606353 | in-del | -/CT | 0.00755907 | 0.0610114 | intron-variant | VCP | GRCh38.p7 | 9:35071163 | TTTCAGAATAAGTGA[-/CT]CTTTTAAATAAGCAA | 7415 |
rs142039727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35062827 | CTTCCCTTTATTGCT[C/T]TTCTGTCTGTAACAT | 7415 |
rs142113644 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VCP | GRCh38.p7 | 9:35058210 | TTAGTTCATCAGTAG[C/T]TGTTAAGCTTTTATG | 7415 |
rs142441131 | snp | C/T | 0.00835141 | 0.0640778 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073793 | TAGCACTCAACTAGA[C/T]GGTCACAAGCCTTCC | 7415 |
rs142577424 | snp | C/T | 0.00526873 | 0.0510549 | synonymous-codon | VCP | GRCh38.p7 | 9:35059793 | CACACAGGGGGCAGC[C/T]TGGCGGGCCTGTAGG | 7415 |
rs142590753 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VCP | GRCh38.p7 | 9:35066405 | TAGCTGGGATTACAG[A/G]TGCCCACGATGGGGT | 7415 |
rs142873785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064797 | GGTAAATCCAAGAAA[C/T]AATTAGGCCCAGAAA | 7415 |
rs143410274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35057810 | AACTTTTTGAGATAG[C/T]AGAAATTTTAAGTCT | 7415 |
rs143484721 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35060132 | CCAGACCCTGTCTCA[A/C]GAGAGAGAGAGAGAA | 7415 |
rs143804260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35070028 | GTGCTCAGCTAGGAA[C/G]CCATGGGGTTCTTAC | 7415 |
rs143957772 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VCP | GRCh38.p7 | 9:35071396 | CGCTTTCCTAAGGAT[A/G]GAGGTGGGGTCAGAA | 7415 |
rs143997916 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VCP | GRCh38.p7 | 9:35068904 | AAAATGCTTAACATA[A/G]TACCTGGCACATGGT | 7415 |
rs144026671 | in-del | -/ATA | 0.0566069 | 0.158427 | intron-variant | VCP | GRCh38.p7 | 9:35068844 | AAAAGAAGGAATATA[-/ATA]CTTATCTCAGAGGCT | 7415 |
rs144304208 | snp | C/G | 0.00592901 | 0.0541235 | intron-variant | VCP | GRCh38.p7 | 9:35060937 | CACTAGAAAAGGAGG[C/G]AAAACTGGGGATGAG | 7415 |
rs144363742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35059343 | CCCCATTTTATTCCT[G/T]ATTCTAGATTATCTT | 7415 |
rs144562700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35061806 | AATGCCAGCACTAAA[A/G]AAGTCTCAAGCTCTG | 7415 |
rs144675858 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35064557 | CTCCTCTAAAGGGAT[A/C]CGGCCTCAAAGAACA | 7415 |
rs144932462 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35062584 | GAACTGTAAAGGTGA[A/C]AGCAAATGCTCTAGG | 7415 |
rs145058305 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VCP | GRCh38.p7 | 9:35059009 | CCAGGGCATGGTGGT[A/G]GCTGCTGCCTGGCTC | 7415 |
rs145308493 | snp | A/G | | | downstream-variant-500B | VCP | GRCh38.p7 | 9:35056038 | TCTATTTTCTGTTTG[A/G]AAAAAAAAAAAATTC | 7415 |
rs145317122 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | VCP | GRCh38.p7 | 9:35069584 | CAGCCTCCCGAGTAG[C/T]TGGGATTACAGGCAT | 7415 |
rs145508640 | snp | A/G | 0.000561019 | 0.016739 | synonymous-codon | VCP | GRCh38.p7 | 9:35057132 | TTAGCCATACAGGTC[A/G]TCATCATTGTCTTCT | 7415 |
rs145619622 | in-del | -/A | 0.0566069 | 0.158427 | intron-variant | VCP | GRCh38.p7 | 9:35069338 | ACTGGGTCTACACTC[-/A]AGTGTTATTTCCTAG | 7415 |
rs145786843 | snp | C/T | 0.000155724 | 0.00882258 | | | GRCh38.p7 | 9:35060564 | TCAAGGCTACCTCCA[C/T]ATTTTGAAAGAAACC | 7415 |
rs145910791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35063439 | GACTAGCTAAGCCAT[G/T]TAAGAGAGCAGGGTC | 7415 |
rs146162084 | in-del | -/G | | | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072385 | GCCGGCGGCTGTGGC[-/G]GGCCCGCGGGTAACG | 7415 |
rs146349079 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073832 | TATATGTAGTAGGCA[A/G]ACGAGATAAATATGA | 7415 |
rs146361426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35070389 | CTTGCTTGACTTATA[A/G]AACTGGGACTGGAGA | 7415 |
rs146365533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058299 | ATTAAGTCCCATGTT[G/T]GGAACTTAATGAATT | 7415 |
rs146628374 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35069011 | CTCCCTTGAGGCTCA[A/G]GGAGGCCTTAAGTTC | 7415 |
rs146658966 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | VCP | GRCh38.p7 | 9:35067735 | CAGAACCAAAACCTA[A/C]AGACAACCCTGAAGC | 7415 |
rs146677446 | snp | C/T | 0.000131778 | 0.00811614 | intron-variant | VCP | GRCh38.p7 | 9:35062939 | AAGCCCAGTTCAAAA[C/T]TGGGTCTAGCTAGAC | 7415 |
rs146927852 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056627 | GTTTAGAAACTGCTT[A/G]TGATTAGTTTTCCAA | 7415 |
rs147070487 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VCP | GRCh38.p7 | 9:35069899 | ATTCATGAGTCTCTA[C/T]TATGTACCAGGCATT | 7415 |
rs147093515 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073357 | AGAAAACTGCATATG[C/T]TGGGACTTGAAAATC | 7415 |
rs147398333 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | VCP | GRCh38.p7 | 9:35061849 | GTCTCAGGAAAACCA[C/G]GGTGGTTGGTCACTC | 7415 |
rs147421533 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VCP | GRCh38.p7 | 9:35065040 | GCCTGGCTAATTTTT[C/G]TATTTTTAGTAGAGA | 7415 |
rs147623367 | snp | A/G | 0.00136651 | 0.0261034 | synonymous-codon | VCP | GRCh38.p7 | 9:35060424 | ATTAGCAATGGCTTT[A/G]GCCAACAAAGTTTTC | 7415 |
rs147680945 | snp | C/G | 0.00279162 | 0.0372561 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073747 | CAAGTTCATAAGGTA[C/G]ACGATGTCAGGAAAG | 7415 |
rs147834079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35059345 | CCATTTTATTCCTGA[C/T]TCTAGATTATCTTGA | 7415 |
rs148311161 | snp | A/G | 1.6546e-05 | 0.00287624 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074059 | AAAGCCCTCCCCACA[A/G]AGAGACAGCCCACTG | 7415 |
rs148329626 | snp | C/T | 0.000824307 | 0.0202848 | missense | VCP | GRCh38.p7 | 9:35061172 | TGCCCGTGAGTCTCA[C/T]TGGCTACCTGCAGAG | 7415 |
rs148380532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057888 | TGGAAATGGTATATA[A/G]AAAGAGTGAATTTTA | 7415 |
rs148671749 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35071182 | TTTAAATAAGCAACT[A/C/G]AGTAATACTTTATCC | 7415 |
rs148971629 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073221 | TTTGCAGTTTCTCAG[C/T]GCTTGTGCCTTTCTT | 7415 |
rs149059712 | snp | C/G/T | 0.00398691 | 0.0444912 | intron-variant | VCP | GRCh38.p7 | 9:35062780 | CAATCTTTCTCAAAG[C/G/T]GGGCAGGACAGGGAG | 7415 |
rs149175694 | in-del | -/TGCCC | | | intron-variant | VCP | GRCh38.p7 | 9:35070825 | TGGAGATGAGTGGTA[-/TGCCC]TGCCCTTTTCTTAAG | 7415 |
rs149380309 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VCP | GRCh38.p7 | 9:35064408 | AGAAGATTCTCAACC[C/T]GGCATGGTGGCTCAC | 7415 |
rs149546996 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | VCP | GRCh38.p7 | 9:35070777 | TGTATCCTAGGAAAA[C/G]CTCCATTCTGCCTAC | 7415 |
rs149634328 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056713 | CAACTGTGGCCCCTA[A/C]CCACCTACCCAGGTT | 7415 |
rs149705391 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | VCP | GRCh38.p7 | 9:35067634 | TTACACCTCTAGTAG[A/G]AAAAAATAAAGCCAT | 7415 |
rs149858552 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VCP | GRCh38.p7 | 9:35072191 | CTGCCGGGTCCACGG[C/T]CCCTCACTCGCCCCC | 7415 |
rs149934660 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VCP | GRCh38.p7 | 9:35062551 | AGCCCAGGGACTCAC[C/T]ATACTCTTCTCACAG | 7415 |
rs150093181 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35060052 | TAGGAGAATTGCTTA[A/C]GCCCAGGTTTCAAGG | 7415 |
rs150203467 | snp | A/G | 1.64817e-05 | 0.00287064 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074136 | GACTTTGGCAGAGAT[A/G]TCCGAAATTCTTCAA | 7415 |
rs150251323 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VCP | GRCh38.p7 | 9:35064099 | GATTAGACATTGGGA[C/T]AGGATTAGACATTGG | 7415 |
rs150564851 | snp | A/C | 0.0618563 | 0.164627 | intron-variant | VCP | GRCh38.p7 | 9:35066458 | TCTCAAACTCCTGGC[A/C]TCAAGTGATCCACCC | 7415 |
rs150614543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058870 | AGACTGAGAATGGAG[A/C]CTGACCATCTCTTCT | 7415 |
rs150826281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35061410 | ATGCAGCGTCAACTA[C/T]GAAAAATGCCAACTC | 7415 |
rs150926717 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | VCP | GRCh38.p7 | 9:35059854 | CTAGATGTCTCTAGG[C/T]AAACGTGGTGGCTCA | 7415 |
rs151222857 | snp | A/G | 0.000131778 | 0.00811614 | synonymous-codon | VCP | GRCh38.p7 | 9:35067983 | ATCATCAGAAAGGAC[A/G]ATGCAAACAGCTTCT | 7415 |
rs151286805 | in-del | -/AAAAAC | | | intron-variant | VCP | GRCh38.p7 | 9:35058792 | AAAAAACAAAAAACA[-/AAAAAC]AAAAAAACCTTGCTG | 7415 |
rs180782795 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VCP | GRCh38.p7 | 9:35064551 | AAGATTCTCCTCTAA[A/G]GGGATCCGGCCTCAA | 7415 |
rs180798421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060698 | GTAGGTTCCTAAGTC[A/G]TGCTCTCACAACTCT | 7415 |
rs180999023 | snp | A/G | 1.64906e-05 | 0.00287142 | synonymous-codon | VCP | GRCh38.p7 | 9:35060487 | CTTGGAAGGTGTCAT[A/G]CCAAACTTCAGGAAT | 7415 |
rs181042539 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35067601 | TGGTATCCTAAGCCA[A/G]GATATAAGTATGATA | 7415 |
rs181215516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071979 | CCGGACGGCAGACTG[A/G]CGCCCCAAAGCCCCG | 7415 |
rs181282686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35064971 | CTCCTGGGTTCAACC[A/G]ATTCTCCTGCCTCAG | 7415 |
rs181736263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058529 | GCACTTTGGGAGGCC[C/G]AGGTGGGCACATCAC | 7415 |
rs181936358 | snp | C/T | 3.38679e-05 | 0.00411495 | intron-variant | VCP | GRCh38.p7 | 9:35059259 | TAGCATTTAGCCTCT[C/T]CTCTCGAGATACGCA | 7415 |
rs182097166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069029 | AGGCCTTAAGTTCTA[A/C]CAAGCAAGCCTGGGG | 7415 |
rs182122614 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073490 | TTGACTAAGACGAGT[C/T]GAATTTCTAGAATTT | 7415 |
rs182647498 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35065926 | AGGTCAAGAGTTCGA[A/G]ACGAGCCTGACCAAC | 7415 |
rs182660810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074616 | ACTCACATATGGAAG[C/T]GGGGGCAGATCATTC | 7415 |
rs182678757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35062711 | CTCTCAAATCACTAA[C/T]CATTCACCCTTTGAT | 7415 |
rs182875014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069953 | AGTCAACAAAACAAG[A/G]CAAAATAGTATTCCC | 7415 |
rs182963009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067151 | TAACAATTGTCAGGG[C/T]CAGTGAAACAGAAGT | 7415 |
rs182965931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069384 | ACCAGACAGTGACAC[C/G]AACTTATTACCTAGC | 7415 |
rs182998839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065755 | GATCCATAAAGATAG[C/T]TTACTCTCCTGGAAC | 7415 |
rs183223259 | snp | C/T | 0.00055992 | 0.0167226 | intron-variant | VCP | GRCh38.p7 | 9:35061574 | CCATCATCATCACTT[C/T]ACCTGTTCCAGGTCC | 7415 |
rs183476007 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056540 | CCAGGAAAAGAAGCA[A/G]GCACAGGGCCCAGGA | 7415 |
rs183508541 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VCP | GRCh38.p7 | 9:35060712 | CGTGCTCTCACAACT[A/C]TTGCAGCAAATGTGT | 7415 |
rs183561716 | snp | C/G | 0.00557542 | 0.0525036 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055948 | AATTTATTTTCTCTG[C/G]ACTACTCTCTCTCTG | 7415 |
rs183694325 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35071086 | ATGATGCCAGGTTCC[A/C]AGAATTTTAGATTTT | 7415 |
rs183916253 | snp | A/G | 0.00320762 | 0.039919 | intron-variant | VCP | GRCh38.p7 | 9:35068105 | GGTCATTGGGCTGAC[A/G]GGGAGTAAGCAGCAG | 7415 |
rs184152880 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072620 | CGCAGACGCTTCGCT[A/G]AGACTGAGCCGAGAA | 7415 |
rs184248829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067592 | ACCCTCGAGTGGTAT[C/G]CTAAGCCAGGATATA | 7415 |
rs184626988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067403 | TCACATTGAGAGCTA[G/T]CCCAGGTCTGGCTCC | 7415 |
rs184846061 | snp | C/G | 0.000635675 | 0.0178167 | intron-variant | VCP | GRCh38.p7 | 9:35057571 | AGGGCTAGTTAAAGC[C/G]CAGCCTGGATTTCAT | 7415 |
rs184862122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064362 | TTCTCTAAATCATTC[C/T]ACTACCTAGTGTGCA | 7415 |
rs185101146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35063740 | CAATAGTTCTCAAAT[A/G]TTTTAGACTCAGAAC | 7415 |
rs185234380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058871 | GACTGAGAATGGAGC[C/T]TGACCATCTCTTCTC | 7415 |
rs185360895 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073895 | GAAAAAAGGTGCCTC[A/G]AGCAAAGTCAATGAC | 7415 |
rs185509438 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VCP | GRCh38.p7 | 9:35070338 | GCTCTCCCACTCCTG[C/T]CCCATCAAAATACTC | 7415 |
rs185906221 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35068616 | AGTGATCCTGCCCCA[C/G]GGTCAGAAAATAATG | 7415 |
rs186007320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064559 | CCTCTAAAGGGATCC[A/G]GCCTCAAAGAACAAC | 7415 |
rs186169208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35065765 | GATAGCTTACTCTCC[C/T]GGAACAGAGAAGGGG | 7415 |
rs186433370 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VCP | GRCh38.p7 | 9:35060624 | TTCATGGTGTACCCA[A/G]TGGTATCAGATCCAG | 7415 |
rs186590981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35059407 | CAACCCTAACCCCAG[C/T]GGAATCTTGTCCAGA | 7415 |
rs186657793 | snp | A/G | 0.000596273 | 0.0172563 | synonymous-codon | VCP | GRCh38.p7 | 9:35057498 | AAAGTGATCTCGACG[A/G]ATCTCAGGCACTGGA | 7415 |
rs186741682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065470 | GGGTCAAAATGCCAA[C/G]CTCATTAGATAGTGC | 7415 |
rs186780925 | snp | A/G | 1.64773e-05 | 0.00287026 | missense | VCP | GRCh38.p7 | 9:35061067 | ACCTCGGCATCAATG[A/G]TCTCATCCTCTAGGT | 7415 |
rs187072010 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VCP | GRCh38.p7 | 9:35069516 | GGAATGCAATGCTGC[A/G]ATCTCAGCTAACTGC | 7415 |
rs187308290 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35067225 | AGGAAGTGACTAAGC[A/C]CTCCCAAGAAGAAAG | 7415 |
rs187516197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069955 | TCAACAAAACAAGAC[A/G]AAATAGTATTCCCAT | 7415 |
rs187604293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066177 | GGCTCATGCCTGTAA[A/T]CCCAGCACTTTGGGA | 7415 |
rs187649317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069098 | GCTAAACCTACTGAT[A/G]CCAGGGCATTCCATA | 7415 |
rs187911930 | snp | C/T | 0.000698161 | 0.0186707 | intron-variant | VCP | GRCh38.p7 | 9:35062387 | ACAATAACAAAATGA[C/T]AGTCTTTCCCAATTC | 7415 |
rs188129823 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VCP | GRCh38.p7 | 9:35063387 | GGCAAGAGGCCATTA[C/T]ACTAAGGGCTCAATT | 7415 |
rs188258544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35059439 | ACTAAAGAGCACTCC[A/G]TACCAGCCTGAGGAC | 7415 |
rs188409958 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VCP | GRCh38.p7 | 9:35071087 | TGATGCCAGGTTCCA[A/T]GAATTTTAGATTTTT | 7415 |
rs188654803 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | VCP | GRCh38.p7 | 9:35068225 | TAAGTGCAGTAAGGA[A/G]AGACTAGTCTGTGGC | 7415 |
rs188935092 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056077 | AATTTTATATTAACA[A/G]AAAGTTTTTTTTTTT | 7415 |
rs189065388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35063939 | TGTTTTGTGCGCACA[C/T]GCACACAACAGACAA | 7415 |
rs189151613 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VCP | GRCh38.p7 | 9:35067597 | CGAGTGGTATCCTAA[A/G]CCAGGATATAAGTAT | 7415 |
rs189188937 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35070397 | ACTTATAGAACTGGG[A/C]CTGGAGAAAAATAAA | 7415 |
rs189340372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067457 | ACTTAGGGGCTTAAA[A/G]GACCTGCTAGCAGCT | 7415 |
rs189588564 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35064465 | CAGAGGTGGGAGGAA[A/T]GCTTGAGTCCAGGAG | 7415 |
rs189679898 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35064790 | GGCATTAGGTAAATC[C/T]AAGAAACAATTAGGC | 7415 |
rs189728374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058190 | TATGTGACTACCTCC[G/T]AGGATTAGTTCATCA | 7415 |
rs189955281 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073042 | TAACCCATACACCCA[A/T]CTTCTCCCAAAACCT | 7415 |
rs190050556 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073942 | TTGTTTCCTCCAAAA[C/G]GAGAATGGTAGTAAC | 7415 |
rs190315689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069771 | CTCTTTTTTAAGAGC[A/G]GCCTCGTGTTAGTAA | 7415 |
rs190474237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35058901 | CGGCCTTATTCCAAA[C/T]TGAATGGATTCACCT | 7415 |
rs190701496 | snp | A/G | 3.29473e-05 | 0.00405864 | intron-variant | VCP | GRCh38.p7 | 9:35061549 | TAGAGACACTGTAAC[A/G]CCTGGTCAGCCATCA | 7415 |
rs190709577 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VCP | GRCh38.p7 | 9:35068879 | TTGTCTTAAGGGAGA[C/T]AATGAATGTAAAATG | 7415 |
rs190729150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069145 | AAGCATAAAGACCAT[A/C]ATATTTGGAAAAAAC | 7415 |
rs190973340 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | VCP | GRCh38.p7 | 9:35065825 | AAAAAGAGGGTAAGA[C/T]ATATGAATATGTGTG | 7415 |
rs191219066 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35062628 | GCAAGAGAGATGGCA[C/T]ACCAGATGGCACACC | 7415 |
rs191280377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060636 | CCAATGGTATCAGAT[C/T]CAGGTTCTCTAGAAG | 7415 |
rs191464167 | snp | A/G | 0.000685647 | 0.0185028 | intron-variant | VCP | GRCh38.p7 | 9:35057566 | TCACTAGGGCTAGTT[A/G]AAGCCCAGCCTGGAT | 7415 |
rs191781695 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055616 | TCCGTGCAACTGTCA[C/T]TGGTATACCTGAGTG | 7415 |
rs192077897 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VCP | GRCh38.p7 | 9:35067308 | GGCCAGGTGATGGTT[C/G]GTTGGGTAGGAGTGG | 7415 |
rs192229770 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VCP | GRCh38.p7 | 9:35070688 | TGATCTGCCTGCCTC[G/T]GCCTCCCAAAATGCT | 7415 |
rs192323336 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35064031 | CTAAAGGATACGTTA[C/T]TGCCCCTCTAATCCA | 7415 |
rs192397114 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073685 | AGGACTAAAGCCACT[A/G]CCTCCAAAGTGAGGA | 7415 |
rs192556285 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056116 | GTACATAAAATAAAG[A/G]TGGACACAACTGTAA | 7415 |
rs192729392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35063534 | GGAATGCTGTTCCTT[A/G]CAATCATCATTTTTC | 7415 |
rs192811170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35066210 | CCATGGCAGATGGAT[C/T]ACTTGAGCCCAGCAG | 7415 |
rs193104260 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VCP | GRCh38.p7 | 9:35067522 | CCCCAACACAAGCCA[A/T]CAATTAGACATACTA | 7415 |
rs193199323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35070009 | AGAGACAAAGAAAAA[C/T]GCTGTGCTCAGCTAG | 7415 |
rs199504528 | snp | A/G | 8.24205e-05 | 0.00641899 | synonymous-codon | VCP | GRCh38.p7 | 9:35062238 | TCTTTTGGGAGCGAT[A/G]GCATCTAGCTCATCA | 7415 |
rs199513619 | snp | A/G | 0.000133304 | 0.00816299 | intron-variant | VCP | GRCh38.p7 | 9:35057536 | CTTCTACCTCCTATA[A/G]TTGGTAAACACAGAT | 7415 |
rs199514126 | snp | C/T | 6.59859e-05 | 0.00574357 | intron-variant | VCP | GRCh38.p7 | 9:35068412 | GCCCCAAGCGCCTCG[C/T]CAGTCTCTAAAACTC | 7415 |
rs199752078 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35060939 | CTAGAAAAGGAGGGA[A/G]AACTGGGGATGAGAC | 7415 |
rs199888265 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066596 | TTAAAAAAAAAAAAA[C/T]AAAAAGAAAATGAGA | 7415 |
rs199891593 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35061711 | GACAGTACACAAACA[A/C]AAACAGGGCTCATCT | 7415 |
rs199892712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065417 | AGCACAGTTAGAGGT[A/G]TCAACTACAAGACAA | 7415 |
rs199895940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064621 | CAGTCCTTGCCTCTC[A/C]CATTACTCGTAGTCT | 7415 |
rs200165441 | snp | C/T | 0.00277021 | 0.0371138 | intron-variant | VCP | GRCh38.p7 | 9:35064327 | AGAAGGCAAGAATAT[C/T]ATATCAGCAAAAGCT | 7415 |
rs200169287 | snp | A/C/G | 3.30323e-05 | 0.0040639 | missense | VCP | GRCh38.p7 | 9:35059540 | TGAGGATGGCAACAC[A/C/G]GGACTTCTCATCAGG | 7415 |
rs200317878 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066582 | AAAGCATAAAAGATT[A/T]AAAAAAAAAAAAAGA | 7415 |
rs200357034 | snp | C/G/T | 0.000232274 | 0.0107743 | intron-variant | VCP | GRCh38.p7 | 9:35065410 | CAGTACAAGCACAGT[C/G/T]AGAGGTGTCAACTAC | 7415 |
rs200358956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071142 | GCATATAAACCAAAA[G/T]AATACTTTCAGAATA | 7415 |
rs200466062 | snp | A/C/G | 0.000164959 | 0.00908057 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074413 | GTTTGGGCCTCCAGC[A/C/G]TCCACCAGAGTGCAG | 7415 |
rs200514532 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VCP | GRCh38.p7 | 9:35058660 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7415 |
rs200548800 | snp | C/T | 1.64953e-05 | 0.00287182 | synonymous-codon | VCP | GRCh38.p7 | 9:35060496 | TGTCATGCCAAACTT[C/T]AGGAATTTGTCTGGG | 7415 |
rs200572118 | snp | C/T | 0.00119856 | 0.0244508 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074521 | GCCCAGAGTACAGAG[C/T]CTTAGAACTTGACAT | 7415 |
rs200670526 | snp | A/G | 0.000595366 | 0.0172432 | synonymous-codon | VCP | GRCh38.p7 | 9:35062330 | CAGACTCACCAGCCA[A/G]TTTGCTCATGATCTC | 7415 |
rs200672216 | snp | C/G | 0.00199798 | 0.0315436 | intron-variant | VCP | GRCh38.p7 | 9:35064306 | TATGGAGGAGATAAA[C/G]AAAGGAGAAGGCAAG | 7415 |
rs200756991 | snp | A/G/T | 0.00329198 | 0.0404375 | intron-variant | VCP | GRCh38.p7 | 9:35061986 | AGGACGGGGTCAAAA[A/G/T]TATCTGGAGTCCTTA | 7415 |
rs200767982 | snp | C/T | 0.000247596 | 0.0111237 | synonymous-codon | VCP | GRCh38.p7 | 9:35057462 | ACTGACAGAACGGCG[C/T]GCAAAGCGCATGGCT | 7415 |
rs200811029 | snp | C/T | 6.85895e-05 | 0.00585577 | intron-variant | VCP | GRCh38.p7 | 9:35059264 | TTTAGCCTCTCCTCT[C/T]GAGATACGCAGATCT | 7415 |
rs200857983 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | VCP | GRCh38.p7 | 9:35064298 | ATCCTGAATATGGAG[A/G]AGATAAAGAAAGGAG | 7415 |
rs200911363 | snp | A/C/T | 6.59091e-05 | 0.00574028 | missense | VCP | GRCh38.p7 | 9:35065315 | ACAATGCAATAAGGG[A/C/T]TAGGATCTGTTTCCA | 7415 |
rs201091341 | snp | A/C | 0.00133804 | 0.0258307 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057113 | GCACGCTGGCCACCA[A/C]CACTTAGCCATACAG | 7415 |
rs201156097 | snp | C/T | 1.65592e-05 | 0.00287738 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057096 | AGGCAGGCCAGCTCA[C/T]TGCACGCTGGCCACC | 7415 |
rs201341281 | snp | C/T | 0.00199806 | 0.0315443 | intron-variant | VCP | GRCh38.p7 | 9:35067865 | CTGGCCTCCCATCCC[C/T]GTGAAGCCAAAAACC | 7415 |
rs201381499 | snp | C/T | 6.58892e-05 | 0.00573936 | synonymous-codon | VCP | GRCh38.p7 | 9:35060867 | TTCCCAGGTTACCTG[C/T]GGCACCTCTACCACG | 7415 |
rs201410035 | snp | A/C | 0.00044469 | 0.0149046 | synonymous-codon | VCP | GRCh38.p7 | 9:35059622 | ATCAATGATGTCAGG[A/C]CGGTTGGTAGCGCCA | 7415 |
rs201413782 | in-del | -/CT | 0.0111196 | 0.0737302 | intron-variant | VCP | GRCh38.p7 | 9:35069752 | CCACAGCACCCAGCG[-/CT]CTCTCTTTTTTAAGA | 7415 |
rs201431036 | snp | C/T | 0.00199806 | 0.0315443 | missense | VCP | GRCh38.p7 | 9:35059797 | CAGGGGGCAGCTTGG[C/T]GGGCCTGTAGGAGGA | 7415 |
rs201437799 | in-del | -/CAGACCCTG | | | intron-variant | VCP | GRCh38.p7 | 9:35060118 | CCTGGGCAACAGAGC[-/CAGACCCTG]TCTCAAGAGAGAGAG | 7415 |
rs201610567 | snp | A/G | 0.000115316 | 0.00759243 | synonymous-codon | VCP | GRCh38.p7 | 9:35063057 | TGTTCCAGGAGGTCC[A/G]TAAAGCAGGATTCCT | 7415 |
rs201890610 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35061696 | CAAAGCGACCTGTGG[C/T]ACAGTACACAAACAT | 7415 |
rs201898330 | snp | A/G | 1.70522e-05 | 0.0029199 | intron-variant | VCP | GRCh38.p7 | 9:35060289 | CAGGCAAATCAATAC[A/G]TAGTTCAGCCTATTG | 7415 |
rs201932327 | snp | C/T | 0.00669109 | 0.0574524 | intron-variant | VCP | GRCh38.p7 | 9:35059032 | CCTGGCTCTCCATGA[C/T]TGGCACATCTGGGGA | 7415 |
rs202025291 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VCP | GRCh38.p7 | 9:35062882 | AAACATGAAGGAGGG[A/G]ATGGGTGCAAAAAGG | 7415 |
rs202090021 | in-del | -/TTTTTTTTTTT | | | intron-variant | VCP | GRCh38.p7 | 9:35069445 | CAAGCTCCCTCTCCC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTG | 7415 |
rs202132829 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066388 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 7415 |
rs202183012 | snp | A/G | 0.0001653 | 0.00908971 | intron-variant | VCP | GRCh38.p7 | 9:35064334 | AAGAATATTATATCA[A/G]CAAAAGCTGAGTTTC | 7415 |
rs267602221 | snp | A/G | | | synonymous-codon | VCP | GRCh38.p7 | 9:35065338 | TGTTTCCACCACTTT[A/G]AACTCCACAGCACGC | 7415 |
rs367575622 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35058539 | AGGCCGAGGTGGGCA[C/T]ATCACAAGGTCAGGA | 7415 |
rs367703031 | snp | A/G | 4.94262e-05 | 0.00497098 | synonymous-codon | VCP | GRCh38.p7 | 9:35066736 | TACCTCGAAGAGATT[A/G]CCAGTAATGCCTTCC | 7415 |
rs367881889 | snp | C/T | 0.000153988 | 0.00877328 | missense | VCP | GRCh38.p7 | 9:35065376 | CACGGACAAGAAAAA[C/T]GTCTCCTGCGAGAGC | 7415 |
rs368003758 | snp | A/G | 6.66289e-05 | 0.00577148 | intron-variant | VCP | GRCh38.p7 | 9:35062399 | TGATAGTCTTTCCCA[A/G]TTCCTCCCAAAAATC | 7415 |
rs368028161 | snp | C/T | 1.65086e-05 | 0.00287298 | intron-variant | VCP | GRCh38.p7 | 9:35057260 | AAAAGAGGGTTAGGA[C/T]AGGGCCTGTGTAAGA | 7415 |
rs368098479 | snp | A/G | 8.23852e-05 | 0.00641762 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074176 | CACGATCAGAGGGAC[A/G]GATCCAGCTCAAATA | 7415 |
rs368178381 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35063302 | AACATTTATGATTGC[A/C]ACTTGCATAGGAGAC | 7415 |
rs368270167 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | VCP | GRCh38.p7 | 9:35062955 | TGGGTCTAGCTAGAC[A/G]TAAGATGAACCAAAT | 7415 |
rs368358470 | snp | C/G | 1.6495e-05 | 0.0028718 | intron-variant | VCP | GRCh38.p7 | 9:35059051 | CACATCTGGGGAAAG[C/G]ATGCAGACTCACCAT | 7415 |
rs368362650 | snp | C/T | 4.94205e-05 | 0.0049707 | intron-variant | VCP | GRCh38.p7 | 9:35061548 | CTAGAGACACTGTAA[C/T]GCCTGGTCAGCCATC | 7415 |
rs368525824 | snp | C/G/T | 5.11525e-05 | 0.00505708 | intron-variant | VCP | GRCh38.p7 | 9:35060555 | AAAGAGGGTTCAAGG[C/G/T]TACCTCCACATTTTG | 7415 |
rs368539027 | snp | C/G | 1.64792e-05 | 0.00287042 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074338 | AGGACACCAACTGCC[C/G]CTCAGCCCCAAGCCA | 7415 |
rs368542781 | snp | A/G/T | 0.00021765 | 0.0104298 | intron-variant | VCP | GRCh38.p7 | 9:35057574 | GCTAGTTAAAGCCCA[A/G/T]CCTGGATTTCATCCC | 7415 |
rs368589509 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35070835 | GTGGTATGCCCTTTT[C/G]TTAAGGTAAAGCCTC | 7415 |
rs368639354 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35058618 | AAAAAATACAAAAAA[C/G]TAGCCGGACATGGTG | 7415 |
rs368645352 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | VCP | GRCh38.p7 | 9:35068019 | CTTCTTTCCTTTCAG[C/T]AACACTGTGTCACCT | 7415 |
rs368746906 | in-del | -/CTTAGAACTTG | 0.00400957 | 0.0445949 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074522 | CCCAGAGTACAGAGT[-/CTTAGAACTTG]ACATAGTCTTAGGCA | 7415 |
rs368770422 | snp | C/G | 1.70255e-05 | 0.00291761 | intron-variant | VCP | GRCh38.p7 | 9:35061727 | AAACAGGGCTCATCT[C/G]TAGTCCAGAGGTAAG | 7415 |
rs368909067 | snp | C/T | 3.42777e-05 | 0.00413977 | intron-variant | VCP | GRCh38.p7 | 9:35060286 | CCTCAGGCAAATCAA[C/T]ACATAGTTCAGCCTA | 7415 |
rs368988697 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant | VCP | GRCh38.p7 | 9:35071238 | ACACACCTCAAAAAA[A/C/G]TAATCTCTTCAAGGA | 7415 |
rs368994715 | snp | C/T | 4.9445e-05 | 0.00497193 | intron-variant | VCP | GRCh38.p7 | 9:35065205 | CCACATGATGCCACA[C/T]TGAGTAATCATAAAA | 7415 |
rs369006103 | snp | A/C/T | 3.29453e-05 | 0.00405854 | intron-variant | VCP | GRCh38.p7 | 9:35068235 | AAGGAAAGACTAGTC[A/C/T]GTGGCCACAGCTTAC | 7415 |
rs369094157 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | VCP | GRCh38.p7 | 9:35062985 | TATCTCACCATTGAT[C/T]AAGAAGAAGAAGGCT | 7415 |
rs369422139 | snp | C/T | 1.65002e-05 | 0.00287225 | intron-variant | VCP | GRCh38.p7 | 9:35061965 | GAGAGAAGTAGGACC[C/T]AAGCAAGGACGGGGT | 7415 |
rs369524577 | snp | C/T | 0.000230612 | 0.0107356 | intron-variant | VCP | GRCh38.p7 | 9:35064134 | ACTTTAGACTTGATT[C/T]CAGAGCCCAGGATGC | 7415 |
rs369648801 | snp | A/C/G | 0.000137849 | 0.00830102 | intron-variant | VCP | GRCh38.p7 | 9:35059265 | TTAGCCTCTCCTCTC[A/C/G]AGATACGCAGATCTT | 7415 |
rs369653842 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35060033 | GCTACTCAGGAGGCT[A/G]AAGTAGGAGAATTGC | 7415 |
rs369830702 | snp | A/G | | | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072406 | GCGGGTAACGGCTAC[A/G]AGCGGTGGCAAGCGA | 7415 |
rs369994179 | snp | A/G | 0.000660218 | 0.0181569 | intron-variant | VCP | GRCh38.p7 | 9:35057270 | TAGGACAGGGCCTGT[A/G]TAAGATTTCCACAAC | 7415 |
rs369998866 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066173 | TGATGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 7415 |
rs370000655 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | VCP | GRCh38.p7 | 9:35071806 | CTGTGAGCTTCCCTG[A/C]GCTCGGCGGGCCTTC | 7415 |
rs370020063 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35058951 | TGCCCTATTAAAATT[A/C]TTCTCAGTTAGATGA | 7415 |
rs370027274 | snp | A/G | 6.6411e-05 | 0.00576204 | intron-variant | VCP | GRCh38.p7 | 9:35062375 | TACAGAATGGAGACA[A/G]TAACAAAATGATAGT | 7415 |
rs370246800 | snp | A/G/T | 0.000362734 | 0.0134625 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074244 | AAGGATGATGCCTAA[A/G/T]GGTGAAAGATTGGCA | 7415 |
rs370296303 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | VCP | GRCh38.p7 | 9:35060929 | TCAAGGCCCACTAGA[A/G]AAGGAGGGAAAACTG | 7415 |
rs370342873 | snp | A/C/T | 0.000165042 | 0.00908272 | intron-variant | VCP | GRCh38.p7 | 9:35064324 | AGGAGAAGGCAAGAA[A/C/T]ATTATATCAGCAAAA | 7415 |
rs370501665 | snp | C/T | 0.000181185 | 0.00951628 | intron-variant | VCP | GRCh38.p7 | 9:35060783 | GACAGTGACTCACCC[C/T]GGACCAAGTTGCCCT | 7415 |
rs370700002 | snp | A/C/T | 4.96227e-05 | 0.00498089 | intron-variant | VCP | GRCh38.p7 | 9:35065385 | GAAAAATGTCTCCTG[A/C/T]GAGAGCAAACAGTAC | 7415 |
rs370818171 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | VCP | GRCh38.p7 | 9:35065223 | AGTAATCATAAAATC[A/G]GATACTGGAATCAGG | 7415 |
rs370950631 | snp | G/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074172 | GCGTCACGATCAGAG[G/T]GACGGATCCAGCTCA | 7415 |
rs371041664 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066618 | AAAATGAGATAAAGA[C/T]GTTCCAAGGTTTATT | 7415 |
rs371135569 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35070285 | ACTAGAGGCCAAGCA[A/T]GCTCAATGTGACAGT | 7415 |
rs371173327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35062655 | CACCACTAAACAGCA[C/T]TCTCCAAGAGCCAGT | 7415 |
rs371301612 | snp | A/C/T | 0.000297528 | 0.0121934 | intron-variant | VCP | GRCh38.p7 | 9:35061713 | CAGTACACAAACATA[A/C/T]ACAGGGCTCATCTCT | 7415 |
rs371537385 | snp | C/T | 0.000197668 | 0.00993955 | intron-variant | VCP | GRCh38.p7 | 9:35066858 | TTACCAACCACACTT[C/T]GGGCCCAAGCACTGG | 7415 |
rs371611274 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VCP | GRCh38.p7 | 9:35071014 | AGGGGACTCCACGGG[A/T]CTTGGAAGGGTTTCA | 7415 |
rs371819773 | snp | A/C/G | 3.29871e-05 | 0.00406112 | intron-variant | VCP | GRCh38.p7 | 9:35061735 | CTCATCTCTAGTCCA[A/C/G]AGGTAAGAGACAGGC | 7415 |
rs371847371 | snp | C/T | 3.29473e-05 | 0.00405864 | intron-variant | VCP | GRCh38.p7 | 9:35068095 | AAGGCCTTTGGGTCA[C/T]TGGGCTGACGGGGAG | 7415 |
rs371862385 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant | VCP | GRCh38.p7 | 9:35061004 | ACCTGAGGCACGGGT[A/G]TGGTCCTTACCCGGA | 7415 |
rs371977902 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35063179 | GAATCAGGCTTCAAC[A/C]CTGACAATATTAAGA | 7415 |
rs371985014 | snp | C/T | 6.94288e-05 | 0.00589148 | intron-variant | VCP | GRCh38.p7 | 9:35059271 | TCTCCTCTCGAGATA[C/T]GCAGATCTTTGGGCT | 7415 |
rs371998635 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063520 | GAATTTATCACACTG[C/G]AATGCTGTTCCTTAC | 7415 |
rs372023441 | snp | A/T | 8.36155e-05 | 0.00646535 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074539 | TAGAACTTGACATAG[A/T]CTTAGGCATTGTTTT | 7415 |
rs372506409 | snp | A/G | 0.000148523 | 0.00861624 | intron-variant | VCP | GRCh38.p7 | 9:35064321 | GAAAGGAGAAGGCAA[A/G]AATATTATATCAGCA | 7415 |
rs372528760 | snp | A/T | 1.64735e-05 | 0.00286993 | intron-variant | VCP | GRCh38.p7 | 9:35062956 | GGGTCTAGCTAGACA[A/T]AAGATGAACCAAATA | 7415 |
rs372583061 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon | VCP | GRCh38.p7 | 9:35059067 | ATGCAGACTCACCAT[A/G]GCTGATGGGTTTGTC | 7415 |
rs372638909 | snp | A/G | 0.00013265 | 0.00814294 | intron-variant | VCP | GRCh38.p7 | 9:35059804 | CAGCTTGGCGGGCCT[A/G]TAGGAGGAATGGATT | 7415 |
rs372708154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060653 | AGGTTCTCTAGAAGA[A/C]GACTCCTTAGTGCCT | 7415 |
rs372839296 | snp | A/G | 1.64923e-05 | 0.00287156 | synonymous-codon | VCP | GRCh38.p7 | 9:35062262 | CTCATCAATGAAGAT[A/G]ATGGCAGGAGCATTC | 7415 |
rs373054042 | snp | A/C | 1.64825e-05 | 0.00287071 | intron-variant | VCP | GRCh38.p7 | 9:35061997 | AAAAGTATCTGGAGT[A/C]CTTACCAAATCGCCG | 7415 |
rs373157397 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071915 | CTGGGGCCTCGGGCT[C/G]GCGGGGCCTGCTCTC | 7415 |
rs373161779 | snp | A/G | 6.60229e-05 | 0.00574518 | intron-variant | VCP | GRCh38.p7 | 9:35063107 | TGCAGAGTGTGATTA[A/G]GTTCCCACCTTCTCC | 7415 |
rs373313031 | snp | A/C/T | 0.00755907 | 0.0610114 | intron-variant | VCP | GRCh38.p7 | 9:35065982 | AACACAAAAATTAGC[A/C/T]GGGCGTGGTGGCAGA | 7415 |
rs373339958 | snp | A/G | 0.000197668 | 0.00993955 | intron-variant | VCP | GRCh38.p7 | 9:35068212 | AAAATCCCTCAAGTA[A/G]GTGCAGTAAGGAAAG | 7415 |
rs373355820 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35057859 | TAGAACTTACACACA[C/T]TTGTCATAAAGCATG | 7415 |
rs373514605 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073004 | ATAGACTGAACCCTT[G/T]TATTAGTCTAGTCCT | 7415 |
rs373541331 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35064649 | TCTTACTGAGAAGGG[A/G]TCTCTAAAATCTGAA | 7415 |
rs373578800 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071970 | GGTGGTAGGCCGGAC[A/G]GCAGACTGGCGCCCC | 7415 |
rs373636900 | snp | C/T | 8.23649e-05 | 0.00641683 | intron-variant | VCP | GRCh38.p7 | 9:35060760 | CCAGATCAATTACAA[C/T]GTACTGAGACAGTGA | 7415 |
rs373785808 | snp | A/G | 0.00445982 | 0.0470108 | intron-variant | VCP | GRCh38.p7 | 9:35061976 | GACCTAAGCAAGGAC[A/G]GGGTCAAAAGTATCT | 7415 |
rs373790118 | snp | A/G | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056118 | ACATAAAATAAAGGT[A/G]GACACAACTGTAAGT | 7415 |
rs373796469 | snp | C/G | 3.29908e-05 | 0.00406132 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074264 | AAAGATTGGCAGAAA[C/G]CTGGGCAGCCATACC | 7415 |
rs373800909 | snp | A/C | 1.65723e-05 | 0.00287852 | missense | VCP | GRCh38.p7 | 9:35057501 | GTGATCTCGACGGAT[A/C]TCAGGCACTGGATCA | 7415 |
rs373870246 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35068513 | GCCAAGGTCACGAGG[A/C]GCAGTATCTACCATA | 7415 |
rs373949207 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | VCP | GRCh38.p7 | 9:35057171 | ACTGCCACCTGTGCC[A/G]CCTCCACTGCCCTGA | 7415 |
rs374038595 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35058438 | GGACCCTATCCCTTC[C/T]CCAACCATCAGGGAT | 7415 |
rs374074931 | snp | A/G | 0.000165618 | 0.00909843 | intron-variant | VCP | GRCh38.p7 | 9:35065396 | CCTGCGAGAGCAAAC[A/G]GTACAAGCACAGTTA | 7415 |
rs374391034 | snp | C/T | 0.00547101 | 0.0520151 | synonymous-codon | VCP | GRCh38.p7 | 9:35057477 | CGCAAAGCGCATGGC[C/T]TCTTCAAAGTGATCT | 7415 |
rs374398172 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | VCP | GRCh38.p7 | 9:35062365 | CCTGAAAGGATACAG[A/G]ATGGAGACAATAACA | 7415 |
rs374552017 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VCP | GRCh38.p7 | 9:35061419 | CAACTATGAAAAATG[C/T]CAACTCCCATTTCCT | 7415 |
rs374590435 | snp | A/G | 8.25798e-05 | 0.00642519 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074087 | CTGGGGACCCAGCTC[A/G]AGCTCTTCAAAACGT | 7415 |
rs374723194 | snp | C/T | 6.59076e-05 | 0.00574016 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074175 | TCACGATCAGAGGGA[C/T]GGATCCAGCTCAAAT | 7415 |
rs374812067 | in-del | -/A | | | intron-variant | VCP | GRCh38.p7 | 9:35060155 | GAGAGAAAAAAAAAA[-/A]TAACACTAGGTCTCT | 7415 |
rs375140071 | snp | A/G | 0.000655003 | 0.0180851 | intron-variant | VCP | GRCh38.p7 | 9:35059268 | GCCTCTCCTCTCGAG[A/G]TACGCAGATCTTTGG | 7415 |
rs375262833 | snp | C/T | 6.59174e-05 | 0.00574059 | synonymous-codon | VCP | GRCh38.p7 | 9:35061132 | AGCAGCCTCTGAGCA[C/T]AGGGCTGCTAAGTCA | 7415 |
rs375277990 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35067379 | TTATGCAAGAACAAG[C/T]AAAATCACTCACATT | 7415 |
rs375300874 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant | VCP | GRCh38.p7 | 9:35066859 | TACCAACCACACTTC[A/G]GGCCCAAGCACTGGG | 7415 |
rs375337185 | snp | A/C/G | 3.29523e-05 | 0.00405898 | intron-variant | VCP | GRCh38.p7 | 9:35068381 | GAAGGAGGAAATGGA[A/C/G]TCAGTAGATACTCCT | 7415 |
rs375434781 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066174 | GATGGCTCATGCCTG[C/T]AATCCCAGCACTTTG | 7415 |
rs375560213 | snp | C/G | 1.67128e-05 | 0.00289069 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074518 | CCAGCCCAGAGTACA[C/G]AGTCTTAGAACTTGA | 7415 |
rs375568319 | snp | C/G | 1.64988e-05 | 0.00287213 | intron-variant | VCP | GRCh38.p7 | 9:35063102 | ACCAATGCAGAGTGT[C/G]ATTAGGTTCCCACCT | 7415 |
rs375649091 | snp | A/T | 3.29451e-05 | 0.00405851 | missense | VCP | GRCh38.p7 | 9:35060826 | TCCTGTAGCTCACGT[A/T]TGACATCCTCTAGGC | 7415 |
rs375705533 | snp | C/T | 3.30049e-05 | 0.00406219 | intron-variant | VCP | GRCh38.p7 | 9:35061964 | GGAGAGAAGTAGGAC[C/T]TAAGCAAGGACGGGG | 7415 |
rs375832127 | snp | C/G | 1.65671e-05 | 0.00287807 | intron-variant | VCP | GRCh38.p7 | 9:35063128 | CACCTTCTCCCAAAC[C/G]CTAAAATGGCTTGAC | 7415 |
rs376146381 | snp | A/G | 8.23608e-05 | 0.00641667 | intron-variant | VCP | GRCh38.p7 | 9:35060791 | CTCACCCTGGACCAA[A/G]TTGCCCTACCTGGAC | 7415 |
rs376403715 | snp | G/T | 6.58892e-05 | 0.00573936 | intron-variant | VCP | GRCh38.p7 | 9:35060768 | ATTACAATGTACTGA[G/T]ACAGTGACTCACCCT | 7415 |
rs376427063 | snp | C/T | 5.23912e-05 | 0.0051179 | intron-variant | VCP | GRCh38.p7 | 9:35060268 | ACAGCCTCTATTCCT[C/T]GCCCTCAGGCAAATC | 7415 |
rs376510669 | snp | A/G | 8.23621e-05 | 0.00641672 | synonymous-codon | VCP | GRCh38.p7 | 9:35059634 | AGGCCGGTTGGTAGC[A/G]CCAATGATGAACACA | 7415 |
rs376894472 | snp | A/G | 3.32508e-05 | 0.00407729 | intron-variant | VCP | GRCh38.p7 | 9:35062385 | AGACAATAACAAAAT[A/G]ATAGTCTTTCCCAAT | 7415 |
rs376952639 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | VCP | GRCh38.p7 | 9:35061562 | ACGCCTGGTCAGCCA[C/T]CATCATCACTTCACC | 7415 |
rs376962559 | snp | G/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056606 | TTTACAACATGTCAT[G/T]TTTTGGTTTAGAAAC | 7415 |
rs377125404 | snp | A/G | | | synonymous-codon | VCP | GRCh38.p7 | 9:35059076 | CACCATGGCTGATGG[A/G]TTTGTCTGCCTCTCT | 7415 |
rs377126059 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | VCP | GRCh38.p7 | 9:35059453 | CGTACCAGCCTGAGG[A/C]CTCATGCAAGTCTCC | 7415 |
rs377152021 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35067871 | TCCCATCCCTGTGAA[A/G]CCAAAAACCCCACAC | 7415 |
rs377221802 | in-del | -/A | | | intron-variant | VCP | GRCh38.p7 | 9:35066595 | TTTAAAAAAAAAAAA[-/A]GAAAAAGAAAATGAG | 7415 |
rs377305067 | snp | A/G | 3.30284e-05 | 0.00406363 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074088 | TGGGGACCCAGCTCA[A/G]GCTCTTCAAAACGTG | 7415 |
rs377316335 | snp | A/G | 0.000115311 | 0.00759224 | synonymous-codon | VCP | GRCh38.p7 | 9:35062130 | GCGCCGCTCCACCTC[A/G]CCATGAGTCTGCCAG | 7415 |
rs377559914 | snp | A/G/T | 0.000457755 | 0.0151226 | intron-variant | VCP | GRCh38.p7 | 9:35060574 | CTCCACATTTTGAAA[A/G/T]AAACCTAACTAAACA | 7415 |
rs377702365 | snp | A/G | 0.000148359 | 0.00861149 | intron-variant | VCP | GRCh38.p7 | 9:35068406 | ACTCCTGCCCCAAGC[A/G]CCTCGCCAGTCTCTA | 7415 |
rs377732809 | snp | A/G | 6.59174e-05 | 0.00574059 | intron-variant | VCP | GRCh38.p7 | 9:35065215 | CCACACTGAGTAATC[A/G]TAAAATCGGATACTG | 7415 |
rs386734429 | multinucleotide-polymorphism | AA/GC | | | intron-variant | VCP | GRCh38.p7 | 9:35071776 | GGCCCCGCCGACCCG[AA/GC]TCCAAAAAGGCGGCT | 7415 |
rs387906789 | snp | C/G/T | 1.64895e-05 | 0.00287132 | VCP | 9 | allele_origin=G(germline)/C(germline) | 9:35065352 | GTCCGTGGTGGGATG[C/G/T]GTGCTGTGGAGTTCA | 7415 |
rs387906790 | snp | A/G | | | missense | VCP | GRCh38.p7 | 9:35059723 | GGAGGTAACATTGGA[A/G]ATGGTGGTGGGGCTG | 7415 |
rs397507560 | in-del | -/CTGGATCCGT | | | frameshift-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074174 | AGAAAGCTATTTGAG[-/CTGGATCCGT]CCCTCTGATCGTGAC | 7415 |
rs397700849 | in-del | -/A | 0 | 0 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35056050 | TGGAAAAAAAAAAAA[-/A]TTCAATACTAAAATT | 7415 |
rs398010682 | in-del | -/T | 0 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35066595 | CTCATTTTCTTTTTC[-/T]TTTTTTTTTTTTTAA | 7415 |
rs527345964 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066242 | TTGAGACCAGCCTGG[A/G]CATCATAGTGAGACC | 7415 |
rs527392621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058610 | TACTAAAAAAAAAAT[A/T]CAAAAAACTAGCCGG | 7415 |
rs527568993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064748 | CACTTATATATTTTG[C/G]GTTCAGTCTAGTTTT | 7415 |
rs527606055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064026 | GTAAACTAAAGGATA[C/T]GTTATTGCCCCTCTA | 7415 |
rs527728553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35059902 | CTTTGGGAGGCCAAG[G/T]TGGGAGGATCACTTG | 7415 |
rs527772264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067183 | AAAAAAACAAAATTA[A/T]CTCAGCCAGGTGGTC | 7415 |
rs527975908 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072721 | GCCTCTCCGCGCCTC[A/T]CCCCAGCAACCCGCA | 7415 |
rs528603090 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055902 | TTTTGAGATTATGTC[A/C]CAAAGCCAATCAACA | 7415 |
rs528802621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35068829 | GATGTCCTCCTCTAT[A/G]AAAGAAGGAATATAA | 7415 |
rs528814223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060608 | GCATCCCCTCCATTA[C/T]TTCATGGTGTACCCA | 7415 |
rs528832267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074667 | GTCCATCATCTGCCC[C/G]CTACTCCTGTGCAAC | 7415 |
rs529188048 | snp | C/G | 3.37154e-05 | 0.00410568 | intron-variant | VCP | GRCh38.p7 | 9:35059254 | TACCTTAGCATTTAG[C/G]CTCTCCTCTCGAGAT | 7415 |
rs529589283 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35059987 | AAAATAAAAAATTAG[A/C]CAGATGTGGTGACGC | 7415 |
rs529589351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067708 | GAAATGGATTTTGAA[A/G]TCCCAGGGAGGCAGA | 7415 |
rs529726543 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35062376 | ACAGAATGGAGACAA[A/T]AACAAAATGATAGTC | 7415 |
rs529775081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069633 | AATTTTGCATTTTTA[C/T]TAGAGATGGGGTTTC | 7415 |
rs529800001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35068968 | AAGCATAAGCTAACT[C/T]TCCAGGGAATTAAGT | 7415 |
rs530331147 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056734 | TACCCAGGTTGGATA[C/G]GGGGAAGGGAGGGCT | 7415 |
rs530571127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35061423 | TATGAAAAATGCCAA[C/T]TCCCATTTCCTGGAT | 7415 |
rs531075754 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055971 | TCTCTCTGGGTAAGG[C/T]ATCACTGTACTGACC | 7415 |
rs531647720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058732 | AGATCGTGCCACTGC[A/G]CTCCAGTCTGGGCAA | 7415 |
rs531706748 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072613 | CGACGGTCGCAGACG[C/T]TTCGCTGAGACTGAG | 7415 |
rs531741062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071930 | CGCGGGGCCTGCTCT[C/T]TCCGGGGACCAAAGG | 7415 |
rs531798055 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | VCP | GRCh38.p7 | 9:35066406 | AGCTGGGATTACAGG[G/T]GCCCACGATGGGGTT | 7415 |
rs532023253 | snp | A/C | 0.000513785 | 0.0160196 | synonymous-codon | VCP | GRCh38.p7 | 9:35057504 | ATCTCGACGGATCTC[A/C]GGCACTGGATCATCC | 7415 |
rs532060742 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056759 | AGGGCTCGGGCAGCA[C/T]TGAGTCAAGTGCAGA | 7415 |
rs532167962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35070457 | TTTATTTTTTGAAAC[A/G]GAGTCTCCCTCTGTT | 7415 |
rs532302967 | in-del | -/TT | 0.000148361 | 0.00861152 | FANCG, VCP | 9 | allele_origin=T(germline)/(germline) | 9:35074124 | TACAGGTCACAAGAC[-/TT]TGGCAGAGATGTCCG | 7415 |
rs532330034 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072536 | GTCGGGCGAACAACG[A/C]TGGCTCCTGATCCGC | 7415 |
rs532433688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069724 | CCCAAAGTACTGGGA[C/T]TACAGGCGTGAGCCA | 7415 |
rs532445930 | in-del | -/A | 0.00119737 | 0.0244387 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056733 | CTACCCAGGTTGGAT[-/A]GGGGGAAGGGAGGGC | 7415 |
rs532465925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071856 | TCGGTGGCAGAGCTC[C/T]TGAGGCCTTCACATG | 7415 |
rs532528005 | in-del | -/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056082 | TATATTAACAAAAAG[-/T]TTTTTTTTTTTAATC | 7415 |
rs532545146 | in-del | -/G | | | intron-variant | VCP | GRCh38.p7 | 9:35069640 | ATTTTTACTAGAGAT[-/G]GGGGTTTCACCATGG | 7415 |
rs532631850 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35066941 | CAGGATGGCTTTAGG[A/C]GAAGAGAGGAAGGAG | 7415 |
rs533615960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067392 | AGCAAAATCACTCAC[A/G]TTGAGAGCTATCCCA | 7415 |
rs534065640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057635 | CCTTGCCCTTCCAAT[A/C]CAACCTGAGGTAAGA | 7415 |
rs534082957 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VCP | GRCh38.p7 | 9:35058341 | ACACAAGACATAGTG[A/G]AAAACAAGTGAGATG | 7415 |
rs534094581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065655 | CTGCCATATAGGTAG[A/C]CCAAGTTTTCACTAC | 7415 |
rs534104306 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057026 | GGAGCAGGCTGTGGG[C/T]GCACCCCTGGTCCCT | 7415 |
rs534398232 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35058238 | ATGGGAGAGAGAAGG[A/G]ATGTCACAGACCCTT | 7415 |
rs534412684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067529 | ACAAGCCATCAATTA[C/G]ACATACTAGTGAGAG | 7415 |
rs534556975 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VCP | GRCh38.p7 | 9:35060023 | TATAGTCCCAGCTAC[G/T]CAGGAGGCTGAAGTA | 7415 |
rs534749772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35066570 | AAATACAGGGGAAAA[A/G]CATAAAAGATTTAAA | 7415 |
rs535114710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35058000 | TACATCCTACCTAGC[A/G]GTCTCACTTCCAGTG | 7415 |
rs535188841 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073858 | TATGAAATTTTACTC[A/G]ACAACAGAAAAGGAG | 7415 |
rs535418091 | snp | A/G | | | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074550 | ATAGTCTTAGGCATT[A/G]TTTTATAAAAAGGGA | 7415 |
rs536172113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35059373 | TGATATCCTCAAAAA[C/T]TCTACCTTCCCTTTA | 7415 |
rs536245988 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35067303 | ATCCTGGCCAGGTGA[C/T]GGTTGGTTGGGTAGG | 7415 |
rs536326078 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35068242 | GACTAGTCTGTGGCC[A/T]CAGCTTACCTGGGAC | 7415 |
rs536728418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060643 | TATCAGATCCAGGTT[C/T]TCTAGAAGAAGACTC | 7415 |
rs536743275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35062719 | TCACTAACCATTCAC[A/C]CTTTGATTTCTCATT | 7415 |
rs536747824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35070772 | AAAGCTGTATCCTAG[A/G]AAAACCTCCATTCTG | 7415 |
rs536976028 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073963 | TGGTAGTAACTAGGG[C/G]AAATTTCACAGGCCT | 7415 |
rs537244234 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35068091 | AGTTAAGGCCTTTGG[G/T]TCATTGGGCTGACGG | 7415 |
rs537403356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35061743 | TAGTCCAGAGGTAAG[A/T]GACAGGCCTAGGGTG | 7415 |
rs537411230 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35064020 | CCTTAGGTAAACTAA[A/T]GGATACGTTATTGCC | 7415 |
rs537580402 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35070600 | CATCACCATGCCTGG[C/T]TACTTTTTGCATTTT | 7415 |
rs537730311 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056417 | AGGGTGAGGCAACAG[A/G/T]AGACATCATACCGAT | 7415 |
rs537965176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064954 | CTCACTGCAACCTCC[A/G]ACTCCTGGGTTCAAC | 7415 |
rs538137992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071428 | GCCCCAGAGCCCGGG[C/T]AATTTCTCAATATAG | 7415 |
rs538369629 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056140 | ACTGTAAGTGATCAC[C/T]AACCAGGGGATGTTT | 7415 |
rs538458489 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VCP | GRCh38.p7 | 9:35067482 | GCAGCTCACCTTCCA[C/T]GCCCATACCCCCACC | 7415 |
rs538764784 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VCP | GRCh38.p7 | 9:35071388 | TTATCTAACGCTTTC[C/G]TAAGGATGGAGGTGG | 7415 |
rs538772387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35063513 | CCCTCCAGAATTTAT[C/G]ACACTGGAATGCTGT | 7415 |
rs539020455 | snp | C/T | 9.88875e-05 | 0.00703093 | intron-variant | VCP | GRCh38.p7 | 9:35065203 | TACCACATGATGCCA[C/T]ACTGAGTAATCATAA | 7415 |
rs539064896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057660 | GTAAGATGCTAGGCC[A/G]TGCTTCCTAAAATTG | 7415 |
rs539532413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35072177 | GGCCCCAGCCGGGCC[C/T]GCCGGGTCCACGGCC | 7415 |
rs539851936 | snp | A/G | 0.000399281 | 0.0141238 | splice-donor-variant | VCP | GRCh38.p7 | 9:35062976 | TGAACCAAATATCTC[A/G]CCATTGATCAAGAAG | 7415 |
rs540233037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071822 | GCTCGGCGGGCCTTC[C/T]CCGACCCCGGGCTCC | 7415 |
rs540593608 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071452 | AATATAGCTGGTTGG[A/G]GAAAGGAGTGCGCGC | 7415 |
rs540704870 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | VCP | GRCh38.p7 | 9:35072077 | ATCGGGCGGGCCGGG[C/G]CCTGCATGACACAGC | 7415 |
rs540876383 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073320 | AGAACACACAGCCAA[C/T]TCAGTAGAACCCAAA | 7415 |
rs541019882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060287 | CTCAGGCAAATCAAT[A/C]CATAGTTCAGCCTAT | 7415 |
rs541158521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067627 | TGATAAATTACACCT[C/G]TAGTAGGAAAAAATA | 7415 |
rs541161657 | snp | A/G | 1.65334e-05 | 0.00287514 | intron-variant | VCP | GRCh38.p7 | 9:35059034 | TGGCTCTCCATGATT[A/G]GCACATCTGGGGAAA | 7415 |
rs541224058 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VCP | GRCh38.p7 | 9:35071719 | GCCCTCTCCCTAACA[C/G]TCCTTCACGACTCAG | 7415 |
rs541228815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065427 | GAGGTGTCAACTACA[A/G]GACAAAGTGAGAACT | 7415 |
rs541361877 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072512 | GCTTCCTCCCACCGG[C/T]AGCGAGGCGTCGGGC | 7415 |
rs541421735 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35068858 | AATACTTATCTCAGA[A/G]GCTTATTGTCTTAAG | 7415 |
rs541582645 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074302 | TCAGTGTTCACCACC[A/C]ACAATAGGTCCAAGG | 7415 |
rs541595807 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35057904 | AAAGAGTGAATTTTA[A/T]TGTATTTATATCATA | 7415 |
rs541795781 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35067040 | CACACATTTAGAAAC[C/G]CCACAAAGACATGCA | 7415 |
rs541868979 | snp | C/G | 0.000181307 | 0.00951949 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074209 | TTTCTAGGTACAGGG[C/G]GAGAGACCTGGAGAG | 7415 |
rs541955931 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066155 | AGAAAATGAGACTAG[C/G]CTTGATGGCTCATGC | 7415 |
rs541980846 | snp | A/G | 8.27219e-05 | 0.00643072 | intron-variant | VCP | GRCh38.p7 | 9:35065386 | AAAAATGTCTCCTGC[A/G]AGAGCAAACAGTACA | 7415 |
rs542019919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35072305 | TCCCGGTGCGCGCCG[C/T]CGCAGCAAGCGAACG | 7415 |
rs542234728 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35058049 | CTACCCAGGGTTTCC[C/T]AATGATTGCAATCCT | 7415 |
rs543143468 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055751 | AAATTTTCGAAGAAT[A/G]TTTAGTATTTCTTCC | 7415 |
rs543176596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069214 | CAAAAGGAACTTCAC[A/G]GTAATATCTGCAAAA | 7415 |
rs543629555 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35065398 | TGCGAGAGCAAACAG[C/T]ACAAGCACAGTTAGA | 7415 |
rs543689812 | snp | A/G | 4.94197e-05 | 0.00497066 | synonymous-codon | VCP | GRCh38.p7 | 9:35059115 | CCTAATCTCACTCTC[A/G]ATGGATTCACGGATG | 7415 |
rs543725505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066131 | ACTCTGTCTCAAAAA[A/G]AAAAGAAAAGAAAAT | 7415 |
rs543779544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35070113 | ATGGTAGGCCTTCTG[C/G]TAACCCTCACACATA | 7415 |
rs543961097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35068553 | ATACCCATTCCAGCA[A/G]CTCCTGGTATTTTGA | 7415 |
rs543997351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067668 | GAAAGTTACAGGAAC[A/G]CCAATTTGTCTCAAG | 7415 |
rs544493733 | snp | C/T | 0 | 0 | intron-variant | VCP | GRCh38.p7 | 9:35063677 | CTTCAGTGTGTTCCA[C/T]GGAAACACTTTCCCA | 7415 |
rs544744366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057318 | TAGGACTCCCATCCC[C/T]TTTGGTGTAGGTCCC | 7415 |
rs545533602 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056642 | GTGATTAGTTTTCCA[A/G]CATTAACTCAAAAGC | 7415 |
rs545728409 | in-del | -/AGAT | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35065749 | TTCAGAGATCCATAA[-/AGAT]AGCTTACTCTCCTGG | 7415 |
rs545792962 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072580 | CAGTGGCAGCGGCAG[C/T]GGCAGCGACGACTCA | 7415 |
rs545944206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071629 | CGAGTCATAACATTA[A/C]GGAAAACTGGCTCAA | 7415 |
rs546162212 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056737 | CCAGGTTGGATAGGG[G/T]GAAGGGAGGGCTCGG | 7415 |
rs546450487 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073927 | TGGTGGTGGCAGAGA[C/T]TGTTTCCTCCAAAAC | 7415 |
rs546483047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35068984 | TCCAGGGAATTAAGT[A/G]AGCCAGACAACCTCC | 7415 |
rs546756719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069688 | AACTCCTGACCTCAG[A/G]TGATCTGCCCACCTC | 7415 |
rs547374300 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35063194 | CCTGACAATATTAAG[A/C]ATAAGCCCTCCGCAG | 7415 |
rs547404983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064764 | GTTCAGTCTAGTTTT[C/T]TGAAATTCCTGGCAT | 7415 |
rs547476877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35059903 | TTTGGGAGGCCAAGG[C/T]GGGAGGATCACTTGA | 7415 |
rs547515001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35059290 | GATCTTTGGGCTACC[C/T]GAGCACTCCCAACTA | 7415 |
rs547644545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066231 | AGCCCAGCAGTTTGA[A/G]ACCAGCCTGGGCATC | 7415 |
rs547743761 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057640 | CCCTTCCAATCCAAC[A/C/T]TGAGGTAAGATGCTA | 7415 |
rs547974423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065683 | TACAACCACCAATGG[C/T]AGAACTGTGCACTCT | 7415 |
rs548094708 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056987 | CAGAGTCAGACTGTA[A/G]CTGAACTGTTCAGAC | 7415 |
rs548111088 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35072812 | CCTAGTAACGCCACG[C/T]CAATTGGCCGCAACG | 7415 |
rs548115222 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35069911 | CTATTATGTACCAGG[A/C]ATTGTTCTAAGGGCT | 7415 |
rs548320014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065561 | AGGCAAGATGAGAAA[A/G]GTAAACTGTGAAGAG | 7415 |
rs548417748 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VCP | GRCh38.p7 | 9:35063945 | GTGCGCACACGCACA[A/C]AACAGACAATTTGAT | 7415 |
rs548552690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35063216 | CCTCCGCAGTAAATG[C/T]TAAGAAGACAATTAC | 7415 |
rs548638257 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VCP | GRCh38.p7 | 9:35059334 | CTTTGGCCACCCCAT[C/T]TTATTCCTGATTCTA | 7415 |
rs548785573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071933 | GGGGCCTGCTCTCTC[C/T]GGGGACCAAAGGCTT | 7415 |
rs548850787 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35071785 | GACCCGGCTCCAAAA[A/C]GGCGGCTGTGAGCTT | 7415 |
rs549055160 | snp | A/G | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056668 | AAAGCATGTAAAATA[A/G]ATCAACCTACTCTCT | 7415 |
rs549578835 | snp | A/C | 6.59272e-05 | 0.00574101 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074373 | GCCTGAGCCTCACCA[A/C]AGAGCATCTTCATGT | 7415 |
rs549703397 | snp | C/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057028 | AGCAGGCTGTGGGCG[C/T]ACCCCTGGTCCCTCT | 7415 |
rs549743349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060001 | GCCAGATGTGGTGAC[A/G]CATGCCTATAGTCCC | 7415 |
rs549833961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35058677 | GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCTG | 7415 |
rs549915384 | snp | C/T | 0.000181191 | 0.00951644 | missense | VCP | GRCh38.p7 | 9:35066780 | TGGGCAGCACATGGA[C/T]ACGTTTGCCGTACTT | 7415 |
rs550079187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35059960 | CAACATACTGAGACT[C/T]TGTCTCTACAAAAAA | 7415 |
rs550307347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35068927 | CACATGGTATTAATG[A/G]TCACCATGATTAACA | 7415 |
rs550316267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35061483 | CCAGAAATCAAAACC[C/T]ATCTCCTCACATCTT | 7415 |
rs550543589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066412 | GATTACAGGTGCCCA[C/T]GATGGGGTTTCGCCA | 7415 |
rs550980403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35070703 | GGCCTCCCAAAATGC[C/T]GGGATTACAGGCCTG | 7415 |
rs551290692 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055974 | CTCTGGGTAAGGCAT[C/G]ACTGTACTGACCCTA | 7415 |
rs551323718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35068868 | TCAGAGGCTTATTGT[C/T]TTAAGGGAGATAATG | 7415 |
rs551491321 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35067582 | ATACATACACACCCT[C/T]GAGTGGTATCCTAAG | 7415 |
rs552228643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35069732 | ACTGGGATTACAGGC[A/G]TGAGCCACAGCACCC | 7415 |
rs552253223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065508 | TAGATATTGCCCTAC[C/T]TCTCCCCAACTCCAC | 7415 |
rs552274643 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056895 | CCCTGTTGGTAATTC[A/G]CTCTCCGCCTACCAA | 7415 |
rs552292144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071888 | CGCAAAGTCCACGCC[C/T]ACCGGGCCCGGCTGG | 7415 |
rs552322517 | in-del | -/A | | | intron-variant | VCP | GRCh38.p7 | 9:35058598 | AACCACGTTTCTACT[-/A]AAAAAAAAAATACAA | 7415 |
rs552509793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058234 | TTTTATGGGAGAGAG[A/T]AGGGATGTCACAGAC | 7415 |
rs552695355 | snp | A/C | | | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055811 | GGGATTGTGATTTTC[A/C]GAATTTTAGACTTTA | 7415 |
rs552747991 | snp | C/T | | | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073210 | ATCCCACAGCCTTTG[C/T]AGTTTCTCAGCGCTT | 7415 |
rs552752995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060724 | ACTCTTGCAGCAAAT[A/G]TGTTGACACCCTGAG | 7415 |
rs552890404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060232 | CCAGCACTAAGAATA[C/T]TTCAACCCTCTTAAA | 7415 |
rs553273871 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | VCP | GRCh38.p7 | 9:35068324 | TTGGGACGGTTCTTC[C/T]GTTTGAGAATGGCTG | 7415 |
rs553307826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069328 | AATCAAAGTCGACTG[A/G]GTCTACACTCAGTGT | 7415 |
rs553370942 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057053 | CCCTCTCCTGGGCAA[A/G]CGCCCCCACCCCCAG | 7415 |
rs553403886 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056569 | GACTCAGGCTCCATT[C/T]TGACCCAACGTTTAT | 7415 |
rs553409652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35063424 | AGACCAAGGGCCAAA[C/G]ACTAGCTAAGCCATT | 7415 |
rs553537426 | in-del | -/AT | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35063907 | TGTAAAGAAAAACCC[-/AT]ATATATATGTGTGTG | 7415 |
rs553546812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35062744 | CTCATTCTAGCTTGC[A/T]CCCGCTCTGCAGTCT | 7415 |
rs553704896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064418 | CAACCCGGCATGGTG[A/G]CTCACATCTGTAATC | 7415 |
rs553743801 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | VCP | GRCh38.p7 | 9:35071544 | TGGAAAGGCGCACAA[A/C]ACACGAACTGAGATT | 7415 |
rs554081930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057829 | AATTTTAAGTCTCAA[C/T]TGTGGTAGTAGTTAT | 7415 |
rs554138975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071061 | GTGACCAAGAGGTTA[A/G]AAACAGCTGATGATG | 7415 |
rs554210337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065163 | GTCAGCCACCGCAGC[C/T]GGCCGAGCACCCAGT | 7415 |
rs554311078 | snp | G/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056180 | AGATGCATTAAAAGA[G/T]AGTATAGAGAATATC | 7415 |
rs554688742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058308 | CATGTTTGGAACTTA[A/C]TGAATTAATTAAGGG | 7415 |
rs554742865 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35065077 | TTCACCATGTTGCCC[A/G]GGCTGGTCTTGAACA | 7415 |
rs554801109 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VCP | GRCh38.p7 | 9:35063702 | TTCCCACTAGGAAAA[G/T]ATTGAGAAGCTACAC | 7415 |
rs554897955 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056482 | TCCAGGATTTCACAT[C/T]TGGAAGAATGCCTTG | 7415 |
rs554920983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071441 | GGTAATTTCTCAATA[C/T]AGCTGGTTGGGGAAA | 7415 |
rs555084817 | snp | A/C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35067538 | CAATTAGACATACTA[A/C/G]TGAGAGTAGTGAGGA | 7415 |
rs555251954 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073200 | GGTAACCCCAATCCC[A/G]CAGCCTTTGCAGTTT | 7415 |
rs555422871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066471 | GCCTCAAGTGATCCA[A/C]CCGCCTCAGCCTCCC | 7415 |
rs555454014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067605 | ATCCTAAGCCAGGAT[A/G]TAAGTATGATAAATT | 7415 |
rs555823571 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35058372 | ACAGAGATCTTACCT[G/T]TATGGAACTTACAAA | 7415 |
rs556148771 | snp | C/T | 3.29587e-05 | 0.00405934 | intron-variant | VCP | GRCh38.p7 | 9:35065226 | AATCATAAAATCGGA[C/T]ACTGGAATCAGGGAG | 7415 |
rs556180123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065770 | CTTACTCTCCTGGAA[C/G]AGAGAAGGGGAGAGA | 7415 |
rs556416439 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VCP | GRCh38.p7 | 9:35063342 | AGAAACTGTAGTCCA[A/G]ATGCGTTTGAAGATA | 7415 |
rs556418857 | snp | C/T | 4.94319e-05 | 0.00497127 | intron-variant | VCP | GRCh38.p7 | 9:35060999 | TGTGTACCTGAGGCA[C/T]GGGTGTGGTCCTTAC | 7415 |
rs556476930 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35057844 | CTGTGGTAGTAGTTA[C/T]AGAACTTACACACAC | 7415 |
rs556510142 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066415 | TACAGGTGCCCACGA[C/T]GGGGTTTCGCCATGT | 7415 |
rs556761866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067600 | GTGGTATCCTAAGCC[A/T]GGATATAAGTATGAT | 7415 |
rs556794903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066924 | AAGTGAAAAAGAAAA[A/G]GCAGGATGGCTTTAG | 7415 |
rs556815296 | snp | C/G | | | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074650 | ACCATTCCCATCCCA[C/G]TGTCCATCATCTGCC | 7415 |
rs557411981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35061772 | TGACCAACCATCTCA[G/T]CCAGCACAGGATTGT | 7415 |
rs557547375 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073943 | TGTTTCCTCCAAAAC[A/G]AGAATGGTAGTAACT | 7415 |
rs557606662 | snp | A/G | 6.84803e-05 | 0.00585111 | intron-variant | VCP | GRCh38.p7 | 9:35059463 | TGAGGACTCATGCAA[A/G]TCTCCCACAGCCCAT | 7415 |
rs557643503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066571 | AATACAGGGGAAAAG[C/T]ATAAAAGATTTAAAA | 7415 |
rs557881252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35068504 | GGAAAGGCAGCCAAG[A/G]TCACGAGGAGCAGTA | 7415 |
rs557948455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066119 | GGACAGCGCGACACT[C/T]TGTCTCAAAAAAAAA | 7415 |
rs558110524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069049 | CAAGCCTGGGGACAA[C/T]GAAGCAGAATCATTG | 7415 |
rs558323867 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35064052 | CTCTAATCCAAGGCA[A/G]TAATGAAAGCCATGC | 7415 |
rs558334524 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055589 | ATGTTTCATCTGCTC[A/G]TCACCGTTATATCCG | 7415 |
rs558683133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057668 | CTAGGCCATGCTTCC[A/T]AAAATTGAGTCACTG | 7415 |
rs558712752 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35069900 | TTCATGAGTCTCTAT[A/T]ATGTACCAGGCATTG | 7415 |
rs558750322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35070861 | GCCTCTAATTCCCCA[C/T]CTACCTACTGAGATC | 7415 |
rs559074701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067785 | GGAGGCTTCCTGCAT[C/T]GACAGGTGCCAAGAA | 7415 |
rs559734075 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056739 | AGGTTGGATAGGGGG[A/G]AGGGAGGGCTCGGGC | 7415 |
rs559784332 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35069940 | CTGGGGATACTGAAG[C/T]CAACAAAACAAGACA | 7415 |
rs559924144 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055898 | TGTCTTTTGAGATTA[C/T]GTCCCAAAGCCAATC | 7415 |
rs559967108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35061875 | CACTCTAGACAGGAC[A/G]TAGGGTAAAGGAAAA | 7415 |
rs560001713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35061311 | TATATACTATCAATA[A/C]CTTTATGGGCTGGGT | 7415 |
rs560145873 | snp | A/T | 0.000399281 | 0.0141238 | synonymous-codon | VCP | GRCh38.p7 | 9:35063051 | CTTTCCTGTTCCAGG[A/T]GGTCCGTAAAGCAGG | 7415 |
rs560211269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058682 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 7415 |
rs560275226 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072535 | CGTCGGGCGAACAAC[A/G]CTGGCTCCTGATCCG | 7415 |
rs560282047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35070415 | GGAGAAAAATAAAAC[A/G]CCAGATGCCTCTAGT | 7415 |
rs560536395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064772 | TAGTTTTTTGAAATT[C/T]CTGGCATTAGGTAAA | 7415 |
rs560570697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071848 | GCTCCGCCTCGGTGG[C/G]AGAGCTCCTGAGGCC | 7415 |
rs560622314 | snp | A/G | 0.00786086 | 0.0621984 | intron-variant | VCP | GRCh38.p7 | 9:35072307 | CCGGTGCGCGCCGCC[A/G]CAGCAAGCGAACGGC | 7415 |
rs561343814 | snp | C/G | 3.29886e-05 | 0.00406118 | intron-variant | VCP | GRCh38.p7 | 9:35057368 | TCTAATGCTCCCAAC[C/G]AACTTACCTGAAGCT | 7415 |
rs561587434 | snp | A/C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056722 | CCCCTACCCACCTAC[A/C/T]CAGGTTGGATAGGGG | 7415 |
rs561726970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35059869 | CAAACGTGGTGGCTC[A/C]CACCTGTATTCCCAG | 7415 |
rs561765529 | snp | C/T | 1.72826e-05 | 0.00293956 | intron-variant | VCP | GRCh38.p7 | 9:35059269 | CCTCTCCTCTCGAGA[C/T]ACGCAGATCTTTGGG | 7415 |
rs561791173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071789 | CGGCTCCAAAAAGGC[A/G]GCTGTGAGCTTCCCT | 7415 |
rs561800642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066194 | CCAGCACTTTGGGAG[G/T]CCATGGCAGATGGAT | 7415 |
rs561806714 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35058598 | AAACCACGTTTCTAC[A/T]AAAAAAAAAATACAA | 7415 |
rs561845312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057988 | CCACATTTGGATTAC[A/T]TCCTACCTAGCGGTC | 7415 |
rs562134756 | snp | C/G | 0 | 0 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073729 | TTCCTCATACCCAGA[C/G]TTCAAGTTCATAAGG | 7415 |
rs562165828 | snp | C/T | 4.94694e-05 | 0.00497316 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074237 | GAGAAAGAAGGATGA[C/T]GCCTAAGGGTGAAAG | 7415 |
rs562369137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057896 | GTATATAGAAAGAGT[A/G]AATTTTATTGTATTT | 7415 |
rs562538168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066150 | AGAAAAGAAAATGAG[A/T]CTAGGCTTGATGGCT | 7415 |
rs562566058 | snp | C/G | 1.66935e-05 | 0.00288903 | intron-variant | VCP | GRCh38.p7 | 9:35057549 | TAGTTGGTAAACACA[C/G]ATCACTAGGGCTAGT | 7415 |
rs562574640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065510 | GATATTGCCCTACCT[C/G]TCCCCAACTCCACCC | 7415 |
rs562576713 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073560 | CTGCCTGTCTCTAAG[G/T]AACAGGTACCTGCCC | 7415 |
rs562614922 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072584 | GGCAGCGGCAGCGGC[A/G]GCGACGACTCAAACG | 7415 |
rs562695875 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35064714 | CCACCATCAGCTTTA[C/T]TTCAAAAATGATTTC | 7415 |
rs562705946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071102 | AGAATTTTAGATTTT[A/T]ACTTTTGAAAATAAG | 7415 |
rs562742873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35070663 | CTGGTCTCAAACTCC[C/T]GACCTCAAGTGATCT | 7415 |
rs563393296 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | VCP | GRCh38.p7 | 9:35059154 | GCAAGCACGCTGGCA[A/G]ATCTCTGTCAGGTCA | 7415 |
rs563400414 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35068860 | TACTTATCTCAGAGG[C/T]TTATTGTCTTAAGGG | 7415 |
rs563516701 | snp | C/T | 1.65111e-05 | 0.0028732 | synonymous-codon | VCP | GRCh38.p7 | 9:35059775 | CAGCTCATCAAAGAA[C/T]AGCACACAGGGGGCA | 7415 |
rs563704866 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35071946 | TCCGGGGACCAAAGG[C/T]TTTCGGCGGGTGGTA | 7415 |
rs563833906 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35071349 | CTCTCTATTCTAAAT[G/T]GAATGGGCTGAGGTA | 7415 |
rs563902424 | snp | G/T | | | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35072916 | AGACCCTTTAATCCC[G/T]TAGAGGCGGACTCTC | 7415 |
rs564249854 | snp | A/C/G | 0.000329671 | 0.0128347 | intron-variant | VCP | GRCh38.p7 | 9:35059056 | CTGGGGAAAGGATGC[A/C/G]GACTCACCATGGCTG | 7415 |
rs564539001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069401 | ACTTATTACCTAGCC[C/T]GTTTCCAGCTGTCAC | 7415 |
rs564707477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074337 | TAGGACACCAACTGC[C/T]CCTCAGCCCCAAGCC | 7415 |
rs564742268 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073811 | TCACAAGCCTTCCCA[C/T]GCAAGTATATGTAGT | 7415 |
rs565534943 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon | VCP | GRCh38.p7 | 9:35062067 | CATAACAATCACATG[G/T]GCCCTCTGCTTTAGG | 7415 |
rs565603593 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35066473 | CTCAAGTGATCCACC[C/G]GCCTCAGCCTCCCAA | 7415 |
rs565667489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060004 | AGATGTGGTGACGCA[C/T]GCCTATAGTCCCAGC | 7415 |
rs565784689 | snp | A/G | 0.000132087 | 0.00812565 | intron-variant | VCP | GRCh38.p7 | 9:35064328 | GAAGGCAAGAATATT[A/G]TATCAGCAAAAGCTG | 7415 |
rs566090084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VCP | GRCh38.p7 | 9:35057898 | ATATAGAAAGAGTGA[A/G]TTTTATTGTATTTAT | 7415 |
rs566092808 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35067167 | CAGTGAAACAGAAGT[A/G]AAAAAAACAAAATTA | 7415 |
rs566184043 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056123 | AAATAAAGGTGGACA[C/G]AACTGTAAGTGATCA | 7415 |
rs566321261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35062430 | AGTTATCTTGCTTGT[C/T]TGGCCCAGAGACAGG | 7415 |
rs566577705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069703 | GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTAC | 7415 |
rs566723546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069005 | GACAACCTCCCTTGA[A/G]GCTCAGGGAGGCCTT | 7415 |
rs566869228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057651 | CAACCTGAGGTAAGA[C/T]GCTAGGCCATGCTTC | 7415 |
rs566977748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35061486 | GAAATCAAAACCCAT[A/C]TCCTCACATCTTAAC | 7415 |
rs567128444 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35056002 | CTAGAAGCACTAAGT[A/G]ATTACTGTTGAAGAG | 7415 |
rs567368191 | in-del | -/TTTTTTTTTTT | | | intron-variant | VCP | GRCh38.p7 | 9:35069459 | CTTTTTTTTTTTTTT[-/TTTTTTTTTTT]GAGATGGAGTTTCGC | 7415 |
rs567437567 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | VCP | GRCh38.p7 | 9:35060689 | TAAGAACAGTAGGTT[-/C]CCTAAGTCGTGCTCT | 7415 |
rs567542622 | snp | C/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056901 | TGGTAATTCACTCTC[C/T]GCCTACCAAATGAAA | 7415 |
rs567726291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069915 | TATGTACCAGGCATT[A/G]TTCTAAGGGCTGGGG | 7415 |
rs567879167 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063865 | CAGGGTCCATTGATA[C/G]AAGAATGGCTTTTAT | 7415 |
rs568166937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35058793 | AAAAAACAAAAAACA[A/T]AAAAAACCTTGCTGT | 7415 |
rs568177607 | snp | C/T | | | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055707 | TGTTGTGTTGTTTCT[C/T]AAATAAATACGCTTT | 7415 |
rs568279827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057626 | TATTGGTCTCCTTGC[C/T]CTTCCAATCCAACCT | 7415 |
rs568300800 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057003 | CTGAACTGTTCAGAC[C/T]GGAGAATGGAGCAGG | 7415 |
rs568303458 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | VCP | GRCh38.p7 | 9:35058340 | AACACAAGACATAGT[G/T]GAAAACAAGTGAGAT | 7415 |
rs568303553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35065642 | CAAGTTCTGACTTCT[A/G]CCATATAGGTAGCCC | 7415 |
rs568316951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35063948 | CGCACACGCACACAA[A/C]AGACAATTTGATTAG | 7415 |
rs568340897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065012 | AGCTGGGATTACAGA[C/T]GTGTACCACCATGCC | 7415 |
rs568359829 | snp | C/T | | | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074273 | CAGAAAGCTGGGCAG[C/T]CATACCCCCGCTTTC | 7415 |
rs568440151 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063154 | TTGACTAGCGCTCCA[C/G]AGAGGGTGAGAATCA | 7415 |
rs568665610 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072708 | CGGACTCTCGCCCGC[C/T]TCTCCGCGCCTCTCC | 7415 |
rs568952408 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056907 | TTCACTCTCCGCCTA[C/T]CAAATGAAAATCGCT | 7415 |
rs568982082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35064868 | TTCTCCAAAGAACAC[A/C]CAGTCTTTTTCTTTT | 7415 |
rs568989403 | snp | C/G | 0.000892946 | 0.021111 | intron-variant | VCP | GRCh38.p7 | 9:35063123 | GTTCCCACCTTCTCC[C/G]AAACCCTAAAATGGC | 7415 |
rs569016847 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35071900 | GCCCACCGGGCCCGG[C/G]TGGGGCCTCGGGCTC | 7415 |
rs569070422 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056411 | AGACAAAGGGTGAGG[A/C]AACAGGAGACATCAT | 7415 |
rs569103295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35062600 | AGCAAATGCTCTAGG[A/G]CCTCTGGCTAGAGCA | 7415 |
rs569306376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057712 | CTTGTCAATGCACTC[C/T]GGAAAAGGGAAAACT | 7415 |
rs569660297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066413 | ATTACAGGTGCCCAC[A/G]ATGGGGTTTCGCCAT | 7415 |
rs569697046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065823 | AAAAAAAGAGGGTAA[C/G]ACATATGAATATGTG | 7415 |
rs569735480 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073111 | TTGCTCCTTCTCAAC[A/G]CTGCCTCCAACCACC | 7415 |
rs569924212 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35068431 | TCTCTAAAACTCATA[A/C]TTAGGAAAGAAACAG | 7415 |
rs570009720 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35067631 | AAATTACACCTCTAG[C/T]AGGAAAAAATAAAGC | 7415 |
rs570264627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35059962 | ACATACTGAGACTTT[C/G]TCTCTACAAAAAATA | 7415 |
rs570334452 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35067444 | CTCTCCCGGGTTAAC[A/T]TAGGGGCTTAAAAGA | 7415 |
rs570510222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35072162 | CGCGGGTGCGCAGCT[A/G]GCCCCAGCCGGGCCT | 7415 |
rs570699051 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35062712 | TCTCAAATCACTAAC[C/T]ATTCACCCTTTGATT | 7415 |
rs571023852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35059329 | CCCTTCTTTGGCCAC[C/T]CCATTTTATTCCTGA | 7415 |
rs571172021 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35072974 | GAGTTTATCCTCCTG[C/G]AAGAACGTGGCACAA | 7415 |
rs571224721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35060026 | AGTCCCAGCTACTCA[G/T]GAGGCTGAAGTAGGA | 7415 |
rs571295272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35068189 | AAAAATGAGAAAAGA[A/T]ACCTGGGAAAATCCC | 7415 |
rs571353825 | in-del | -/AAAAAACAAAAAAC | 0.00577057 | 0.053404 | intron-variant | VCP | GRCh38.p7 | 9:35058771 | GACTTCGTCTCAAAA[-/AAAAAACAAAAAAC]AAAAAACAAAAAAAA | 7415 |
rs571494903 | in-del | -/TC | | | intron-variant | VCP | GRCh38.p7 | 9:35069893 | CAACAAATTCATGAG[-/TC]TCTATTATGTACCAG | 7415 |
rs571568392 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35064310 | GAGGAGATAAAGAAA[A/G]GAGAAGGCAAGAATA | 7415 |
rs571628729 | in-del | -/CTC | | | intron-variant | VCP | GRCh38.p7 | 9:35066836 | AGGATGACAAGCAGA[-/CTC]CATATTACCAACCAC | 7415 |
rs571715504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069062 | AACGAAGCAGAATCA[C/T]TGGTGCTACCCTCCT | 7415 |
rs572085032 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | VCP | GRCh38.p7 | 9:35070845 | CTTTTCTTAAGGTAA[A/T]GCCTCTAATTCCCCA | 7415 |
rs572109348 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VCP | GRCh38.p7 | 9:35065955 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAACA | 7415 |
rs572137001 | snp | C/T | 1.65348e-05 | 0.00287526 | intron-variant | VCP | GRCh38.p7 | 9:35059033 | CTGGCTCTCCATGAT[C/T]GGCACATCTGGGGAA | 7415 |
rs572232304 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072490 | ACCCGCAAGCGGCTT[C/T]CCTCTCGCTTCCTCC | 7415 |
rs572451192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067623 | AGTATGATAAATTAC[A/C]CCTCTAGTAGGAAAA | 7415 |
rs572470999 | snp | C/T | 4.9476e-05 | 0.00497348 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074254 | CCTAAGGGTGAAAGA[C/T]TGGCAGAAAGCTGGG | 7415 |
rs573420693 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | VCP | GRCh38.p7 | 9:35065161 | GTGTCAGCCACCGCA[-/G]CCGGCCGAGCACCCA | 7415 |
rs573469169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069383 | CACCAGACAGTGACA[C/T]CAACTTATTACCTAG | 7415 |
rs574182436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35069158 | ATCATATTTGGAAAA[A/G]ACACTAACAGACATC | 7415 |
rs574321642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35068610 | CAAGTGAGTGATCCT[G/T]CCCCAGGGTCAGAAA | 7415 |
rs574415558 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35068854 | ATATAATACTTATCT[C/G]AGAGGCTTATTGTCT | 7415 |
rs574598589 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35070826 | TGGAGATGAGTGGTA[C/T]GCCCTTTTCTTAAGG | 7415 |
rs574719362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35057799 | GTGGCTAAGGAAACT[C/T]TTTGAGATAGTAGAA | 7415 |
rs575080422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071457 | AGCTGGTTGGGGAAA[A/G]GAGTGCGCGCACGTT | 7415 |
rs575421856 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055595 | CATCTGCTCATCACC[A/G]TTATATCCGTGCAAC | 7415 |
rs575501259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35070962 | GGGCAATCCTCCATT[A/G]TCTTCTGTATAAGTC | 7415 |
rs575739675 | snp | A/G | 1.64974e-05 | 0.00287201 | synonymous-codon | VCP | GRCh38.p7 | 9:35057207 | GCCAGCTCCACCCTG[A/G]TTCCCTGAAGGGAAT | 7415 |
rs575777814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VCP | GRCh38.p7 | 9:35063675 | ATCTTCAGTGTGTTC[C/T]ATGGAAACACTTTCC | 7415 |
rs575822739 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056692 | ACTCTCTATATAAAC[A/G]TCCAGCAACTGTGGC | 7415 |
rs576010407 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35058035 | ATATACTCTTAAATC[C/T]ACCCAGGGTTTCCCA | 7415 |
rs576140588 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35062566 | TATACTCTTCTCACA[A/G]TTGAACTGTAAAGGT | 7415 |
rs576163174 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35070915 | TGAATTTGGCCTGAC[C/T]ATGGGCCAACAGCAG | 7415 |
rs576209072 | snp | C/G | 0.000205191 | 0.0101269 | intron-variant | VCP | GRCh38.p7 | 9:35072299 | GGCTGGTCCCGGTGC[C/G]CGCCGCCGCAGCAAG | 7415 |
rs576232546 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35065111 | GACCTCAAGTGATCT[A/G]CCCATCTCAGTCTCC | 7415 |
rs576242998 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35067315 | TGATGGTTGGTTGGG[G/T]AGGAGTGGCTAGAGA | 7415 |
rs576848304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071588 | GAACCTAAAATGTTA[A/G]AGAAAAATTCCTTTC | 7415 |
rs576892457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35071092 | CCAGGTTCCAAGAAT[C/T]TTAGATTTTTACTTT | 7415 |
rs577126030 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VCP | GRCh38.p7 | 9:35057855 | GTTATAGAACTTACA[A/C]ACACTTGTCATAAAG | 7415 |
rs577185031 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35065826 | AAAAGAGGGTAAGAC[A/G]TATGAATATGTGTGC | 7415 |
rs577476678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35065168 | CCACCGCAGCCGGCC[A/G]AGCACCCAGTCCTGA | 7415 |
rs577500778 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073962 | ATGGTAGTAACTAGG[A/G]CAAATTTCACAGGCC | 7415 |
rs577536034 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073444 | TATGCTGACTCAATT[C/T]ACCTTTCACCCTGTA | 7415 |
rs577663447 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35061427 | AAAAATGCCAACTCC[C/T]ATTTCCTGGATTCAA | 7415 |
rs577805218 | snp | A/T | 0.000399281 | 0.0141238 | synonymous-codon | VCP | GRCh38.p7 | 9:35059073 | ACTCACCATGGCTGA[A/T]GGGTTTGTCTGCCTC | 7415 |
rs577812326 | snp | C/T | 4.99247e-05 | 0.00499598 | synonymous-codon | VCP | GRCh38.p7 | 9:35066694 | CCGGATGGGTCGATA[C/T]GCTTCCAGGAAGTAC | 7415 |
rs577843887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35066121 | ACAGCGCGACACTCT[A/G]TCTCAAAAAAAAAAG | 7415 |
rs578132371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35068527 | GAGCAGTATCTACCA[C/T]ACATATTACAATACC | 7415 |
rs578158002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VCP | GRCh38.p7 | 9:35067667 | AGAAAGTTACAGGAA[C/T]GCCAATTTGTCTCAA | 7415 |
rs745489582 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | VCP | GRCh38.p7 | 9:35061557 | CTGTAACGCCTGGTC[A/G]GCCATCATCATCACT | 7415 |
rs745585033 | snp | G/T | 8.23662e-05 | 0.00641688 | intron-variant | VCP | GRCh38.p7 | 9:35066857 | ATTACCAACCACACT[G/T]CGGGCCCAAGCACTG | 7415 |
rs745690473 | snp | C/T | 4.95724e-05 | 0.00497833 | synonymous-codon | VCP | GRCh38.p7 | 9:35066709 | CGCTTCCAGGAAGTA[C/T]GGCTTAAGGTATACC | 7415 |
rs745725271 | snp | A/G | | | synonymous-codon | VCP | GRCh38.p7 | 9:35059777 | GCTCATCAAAGAATA[A/G]CACACAGGGGGCAGC | 7415 |
rs745794060 | snp | C/T | 5.24976e-05 | 0.00512309 | intron-variant | VCP | GRCh38.p7 | 9:35060263 | GAAAAACAGCCTCTA[C/T]TCCTTGCCCTCAGGC | 7415 |
rs745885712 | snp | C/T | 1.65091e-05 | 0.00287303 | intron-variant | VCP | GRCh38.p7 | 9:35063109 | CAGAGTGTGATTAGG[C/T]TCCCACCTTCTCCCA | 7415 |
rs746014417 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35068538 | ACCATACATATTACA[A/C]TACCCATTCCAGCAG | 7415 |
rs746060480 | snp | A/G | 1.65045e-05 | 0.00287263 | synonymous-codon | VCP | GRCh38.p7 | 9:35062283 | AGGAGCATTCTTCTC[A/G]GCCTCCTCAAAGGCT | 7415 |
rs746078275 | snp | C/T | 8.23825e-05 | 0.00641751 | intron-variant | VCP | GRCh38.p7 | 9:35068386 | AGGAAATGGAGTCAG[C/T]AGATACTCCTGCCCC | 7415 |
rs746167710 | snp | C/G | 1.64944e-05 | 0.00287175 | missense | VCP | GRCh38.p7 | 9:35057199 | TGACTGGGGCCAGCT[C/G]CACCCTGGTTCCCTG | 7415 |
rs746237606 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | VCP | GRCh38.p7 | 9:35060885 | CACCTCTACCACGGT[C/T]TCCCGCAGTGCTGAT | 7415 |
rs746253368 | snp | A/C | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056543 | GGAAAAGAAGCAGGC[A/C]CAGGGCCCAGGACTC | 7415 |
rs746256928 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35072261 | CGCGCCCACGGCCAG[A/G]CCCCGCCGGGCCTAC | 7415 |
rs746343398 | snp | A/C | 6.62372e-05 | 0.0057545 | intron-variant | VCP | GRCh38.p7 | 9:35065392 | GTCTCCTGCGAGAGC[A/C]AACAGTACAAGCACA | 7415 |
rs746367183 | snp | A/C | 1.6473e-05 | 0.00286988 | intron-variant | VCP | GRCh38.p7 | 9:35060758 | ACCCAGATCAATTAC[A/C]ATGTACTGAGACAGT | 7415 |
rs746392434 | in-del | -/G | 3.29636e-05 | 0.00405964 | frameshift-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074206 | AGCTTTCTAGGTACA[-/G]GGGGAGAGACCTGGA | 7415 |
rs746458413 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon | VCP | GRCh38.p7 | 9:35065251 | AGGGAGAAAACTCAC[C/T]TCTCGTTTGATAGGC | 7415 |
rs746514004 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35064409 | GAAGATTCTCAACCC[A/G]GCATGGTGGCTCACA | 7415 |
rs746544977 | in-del | -/AAGAGA | | | intron-variant | VCP | GRCh38.p7 | 9:35060131 | GCCAGACCCTGTCTC[-/AAGAGA]GAGAGAGAGAAAAAA | 7415 |
rs746559433 | snp | C/G | 1.67281e-05 | 0.00289202 | intron-variant | VCP | GRCh38.p7 | 9:35059246 | AGCAGAGGTACCTTA[C/G]CATTTAGCCTCTCCT | 7415 |
rs746571026 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35063623 | CATAGAAAATGAAAT[A/T]ATTTGTGTGCCACCC | 7415 |
rs746613103 | snp | C/G | 1.64811e-05 | 0.00287059 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074200 | TCAAATAGCTTTCTA[C/G]GTACAGGGGGAGAGA | 7415 |
rs746617777 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | VCP | GRCh38.p7 | 9:35059098 | TGCCTCTCTCGTTCT[C/T]GCCTAATCTCACTCT | 7415 |
rs746681274 | in-del | -/GTTTTTT | | | intron-variant | VCP | GRCh38.p7 | 9:35071293 | CCTTGGGCTGGCTGT[-/GTTTTTT]TTTTTTTTTTTTTTT | 7415 |
rs746717302 | snp | C/T | | | missense | VCP | GRCh38.p7 | 9:35061582 | ATCACTTCACCTGTT[C/T]CAGGTCCACATCATC | 7415 |
rs746753527 | snp | C/G | 1.67214e-05 | 0.00289144 | intron-variant | VCP | GRCh38.p7 | 9:35057563 | AGATCACTAGGGCTA[C/G]TTAAAGCCCAGCCTG | 7415 |
rs746768696 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35071618 | CTCCCCACCCACGAG[A/T]CATAACATTAAGGAA | 7415 |
rs746810092 | snp | A/T | 6.58957e-05 | 0.00573964 | missense | VCP | GRCh38.p7 | 9:35067956 | CATCCGAATCTTCTC[A/T]TCAGAACAAGTATCA | 7415 |
rs746863687 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35070589 | CAGGTGTGCACCATC[A/G]CCATGCCTGGCTACT | 7415 |
rs746916521 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | VCP | GRCh38.p7 | 9:35066862 | CAACCACACTTCGGG[C/T]CCAAGCACTGGGTGT | 7415 |
rs747021108 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon | VCP | GRCh38.p7 | 9:35060409 | GTTGGCCTGGCATTC[A/G]TTAGCAATGGCTTTG | 7415 |
rs747164485 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066395 | GCCTCCCAGGTAGCT[A/G]GGATTACAGGTGCCC | 7415 |
rs747199521 | in-del | -/G | 0.000165328 | 0.00909046 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074074 | GAGAGACAGCCCACT[-/G]GGGACCCAGCTCAAG | 7415 |
rs747249229 | snp | G/T | 1.6473e-05 | 0.00286988 | synonymous-codon | VCP | GRCh38.p7 | 9:35062982 | AAATATCTCACCATT[G/T]ATCAAGAAGAAGAAG | 7415 |
rs747332989 | in-del | -/G | 1.64947e-05 | 0.00287177 | intron-variant | VCP | GRCh38.p7 | 9:35061976 | GACCTAAGCAAGGAC[-/G]GGGTCAAAAGTATCT | 7415 |
rs747361319 | snp | C/G | 1.64868e-05 | 0.00287109 | synonymous-codon | VCP | GRCh38.p7 | 9:35057414 | CTGCTGAAGGGTCTG[C/G]GCAAACATCTCATAC | 7415 |
rs747488857 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073670 | ATTCAGGCAATGTGA[A/G]GGACTAAAGCCACTG | 7415 |
rs747491775 | snp | C/T | 1.64781e-05 | 0.00287033 | intron-variant | VCP | GRCh38.p7 | 9:35061009 | AGGCACGGGTGTGGT[C/T]CTTACCCGGAAGTCA | 7415 |
rs747614057 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | VCP | GRCh38.p7 | 9:35060912 | TGATGGGTTACTCTG[A/G]CTCAAGGCCCACTAG | 7415 |
rs747659856 | snp | A/G | | | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074638 | AGATCATTCACAACC[A/G]TTCCCATCCCAGTGT | 7415 |
rs747667635 | snp | A/G | 3.31373e-05 | 0.00407032 | intron-variant | VCP | GRCh38.p7 | 9:35065397 | CTGCGAGAGCAAACA[A/G]TACAAGCACAGTTAG | 7415 |
rs747754993 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | VCP | GRCh38.p7 | 9:35065262 | TCACCTCTCGTTTGA[C/T]AGGCTCCCCTTCGCA | 7415 |
rs747772777 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063285 | ACTGCTAGAAAGTGG[A/G]CAACATTTATGATTG | 7415 |
rs747829938 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35064396 | ACCTACCGTATAAGA[A/T]GATTCTCAACCCGGC | 7415 |
rs747842715 | snp | G/T | 1.64795e-05 | 0.00287045 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074340 | GACACCAACTGCCCC[G/T]CAGCCCCAAGCCAGC | 7415 |
rs747902669 | snp | C/T | | | missense | VCP | GRCh38.p7 | 9:35062029 | AGAGCTGGGTCAATG[C/T]TGTTGGGTCTGTTGG | 7415 |
rs747942668 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35068840 | CTATAAAAGAAGGAA[A/T]ATAATACTTATCTCA | 7415 |
rs747975110 | snp | C/T | 1.6498e-05 | 0.00287206 | missense | VCP | GRCh38.p7 | 9:35059129 | CGATGGATTCACGGA[C/T]GGCCAGCTTGCAAGC | 7415 |
rs747998047 | snp | A/C | 1.64746e-05 | 0.00287002 | intron-variant | VCP | GRCh38.p7 | 9:35062190 | GGGCCTTTCAACCCC[A/C]CTCTATCCCCTCAGG | 7415 |
rs748091463 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | VCP | GRCh38.p7 | 9:35067982 | TATCATCAGAAAGGA[C/T]GATGCAAACAGCTTC | 7415 |
rs748148701 | in-del | -/CA | 1.65464e-05 | 0.00287627 | intron-variant | VCP | GRCh38.p7 | 9:35067881 | TGAAGCCAAAAACCC[-/CA]CACACACACCTGATG | 7415 |
rs748189255 | in-del | -/CT | | | intron-variant | VCP | GRCh38.p7 | 9:35071926 | GGCTCGCGGGGCCTG[-/CT]CTCTCCGGGGACCAA | 7415 |
rs748204384 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35058886 | CTGACCATCTCTTCT[C/T]GGCCTTATTCCAAAT | 7415 |
rs748378458 | snp | A/C/G/T | 3.29518e-05 | 0.00405894 | synonymous-codon | VCP | GRCh38.p7 | 9:35060439 | GGCCAACAAAGTTTT[A/C/G/T]CCACAGCCAGGAGGT | 7415 |
rs748447593 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | VCP | GRCh38.p7 | 9:35064269 | TACCCTACTTCATTC[A/G]AGGACTCTTCCTCAT | 7415 |
rs748510332 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35064698 | GGGCAGAGGCCTGAA[C/G]CCACCATCAGCTTTA | 7415 |
rs748535238 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | VCP | GRCh38.p7 | 9:35064123 | ACATTGGCACCACTT[C/T]AGACTTGATTCCAGA | 7415 |
rs748537777 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35065956 | CATGGTGAAACCCCG[C/T]CTCTACTAAAAACAC | 7415 |
rs748619052 | snp | C/T | 1.65034e-05 | 0.00287253 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074100 | TCAAGCTCTTCAAAA[C/T]GTGGCAGCTACAGGT | 7415 |
rs748634605 | snp | C/T | | | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074139 | TTTGGCAGAGATGTC[C/T]GAAATTCTTCAAGGA | 7415 |
rs748644456 | snp | A/G | 1.6661e-05 | 0.00288621 | intron-variant | VCP | GRCh38.p7 | 9:35057533 | CCTCTTCTACCTCCT[A/G]TAGTTGGTAAACACA | 7415 |
rs748730992 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073436 | GTTGGTGATATGCTG[A/G]CTCAATTCACCTTTC | 7415 |
rs748732505 | snp | C/T | 3.29875e-05 | 0.00406112 | missense | VCP | GRCh38.p7 | 9:35057442 | TACTTCCGAATGTCA[C/T]TGTCACTGACAGAAC | 7415 |
rs748816624 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon | VCP | GRCh38.p7 | 9:35061045 | AGTAACTGCTAGAGA[A/G]TTCATGACCTCGGCA | 7415 |
rs748861639 | snp | A/T | 1.67337e-05 | 0.00289251 | synonymous-codon | VCP | GRCh38.p7 | 9:35066688 | ACCTTTCCGGATGGG[A/T]CGATACGCTTCCAGG | 7415 |
rs748899865 | snp | A/G | 1.67407e-05 | 0.00289311 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074527 | AGTACAGAGTCTTAG[A/G]ACTTGACATAGTCTT | 7415 |
rs749042257 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35064806 | AAGAAACAATTAGGC[A/C]CAGAAATGAATAGCT | 7415 |
rs749161429 | snp | A/G | 1.72818e-05 | 0.00293949 | intron-variant | VCP | GRCh38.p7 | 9:35059267 | AGCCTCTCCTCTCGA[A/G]ATACGCAGATCTTTG | 7415 |
rs749229187 | snp | C/G | 1.64735e-05 | 0.00286993 | intron-variant | VCP | GRCh38.p7 | 9:35062948 | TCAAAATTGGGTCTA[C/G]CTAGACATAAGATGA | 7415 |
rs749313890 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35072140 | CGCAAGCCCCGCCTA[A/G]GGGGCGCGCGGGTGC | 7415 |
rs749367752 | snp | C/T | 1.64953e-05 | 0.00287182 | missense | VCP | GRCh38.p7 | 9:35057158 | CTTCTGTGTATACAC[C/T]GCCACCTGTGCCGCC | 7415 |
rs749381324 | snp | A/G | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056735 | ACCCAGGTTGGATAG[A/G]GGGAAGGGAGGGCTC | 7415 |
rs749384898 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | VCP | GRCh38.p7 | 9:35068220 | TCAAGTAAGTGCAGT[A/G]AGGAAAGACTAGTCT | 7415 |
rs749412689 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35057555 | GTAAACACAGATCAC[A/T]AGGGCTAGTTAAAGC | 7415 |
rs749471175 | snp | C/T | 3.29462e-05 | 0.00405857 | synonymous-codon | VCP | GRCh38.p7 | 9:35068004 | AACAGCTTCTCGTCT[C/T]TTCTTTCCTTTCAGC | 7415 |
rs749598999 | snp | A/T | 3.29462e-05 | 0.00405857 | intron-variant | VCP | GRCh38.p7 | 9:35060752 | GAGATCACCCAGATC[A/T]ATTACAATGTACTGA | 7415 |
rs749694177 | snp | G/T | 1.64784e-05 | 0.00287035 | intron-variant | VCP | GRCh38.p7 | 9:35065231 | TAAAATCGGATACTG[G/T]AATCAGGGAGAAAAC | 7415 |
rs749733793 | snp | G/T | 1.64936e-05 | 0.00287168 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074267 | GATTGGCAGAAAGCT[G/T]GGCAGCCATACCCCC | 7415 |
rs749743507 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35064499 | CTGGGCAATACAGCA[A/C]GACTCCATCTCATTA | 7415 |
rs749849000 | snp | C/T | 3.29478e-05 | 0.00405867 | synonymous-codon | VCP | GRCh38.p7 | 9:35062109 | GGTCAACAACTGTGA[C/T]ACAATGCGCCGCTCC | 7415 |
rs749917537 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066980 | GGAAGTGAGGGCGAA[A/G]GAACAGCCCCACTCA | 7415 |
rs749982944 | snp | C/T | 1.65057e-05 | 0.00287273 | intron-variant | VCP | GRCh38.p7 | 9:35061958 | GATGAAGGAGAGAAG[C/T]AGGACCTAAGCAAGG | 7415 |
rs750080784 | snp | C/T | 3.29935e-05 | 0.00406149 | synonymous-codon | VCP | GRCh38.p7 | 9:35067905 | CCTGATGACATCCCC[C/T]AGGCGTACACGAAGG | 7415 |
rs750212705 | snp | C/T | 0.000132065 | 0.00812498 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074429 | TCCACCAGAGTGCAG[C/T]GGCCTCATCCCTCCG | 7415 |
rs750247487 | snp | C/G | 1.64741e-05 | 0.00286998 | synonymous-codon | VCP | GRCh38.p7 | 9:35060397 | GATGGAGATGAAGTT[C/G]GCCTGGCATTCATTA | 7415 |
rs750264849 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071918 | GGGCCTCGGGCTCGC[C/G]GGGCCTGCTCTCTCC | 7415 |
rs750316105 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35061801 | GTCCTAATGCCAGCA[C/T]TAAAAAAGTCTCAAG | 7415 |
rs750335399 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | VCP | GRCh38.p7 | 9:35064165 | TCACCTTCACACCAA[C/T]TGCCTTAAAGAGGGC | 7415 |
rs750419733 | in-del | -/A | 5.34664e-05 | 0.00517014 | intron-variant | VCP | GRCh38.p7 | 9:35066640 | AGGTTTATTCCCTAC[-/A]GTCAATAATCCTTAA | 7415 |
rs750436883 | snp | G/T | 1.64773e-05 | 0.00287026 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074157 | AATTCTTCAAGGAAG[G/T]CGTCACGATCAGAGG | 7415 |
rs750571188 | snp | C/T | 1.65636e-05 | 0.00287776 | missense | VCP | GRCh38.p7 | 9:35057496 | TCAAAGTGATCTCGA[C/T]GGATCTCAGGCACTG | 7415 |
rs750659100 | snp | C/T | 3.29837e-05 | 0.00406088 | intron-variant | VCP | GRCh38.p7 | 9:35057373 | TGCTCCCAACCAACT[C/T]ACCTGAAGCTGCCAA | 7415 |
rs750719844 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35070979 | CTTCTGTATAAGTCA[A/G]TCCCTTTCCAGAACT | 7415 |
rs750823797 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35069671 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 7415 |
rs750970085 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35063807 | TTCTACTGGGTGACA[C/T]TGCTCTAGACAGGCT | 7415 |
rs750971923 | snp | C/T | 3.31164e-05 | 0.00406904 | synonymous-codon | VCP | GRCh38.p7 | 9:35059514 | AACTGGGGACTTGCG[C/T]AGGTTAGCCTTGAGG | 7415 |
rs750982155 | snp | C/T | 3.31669e-05 | 0.00407215 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074469 | CTTCAGAGTCTGAAG[C/T]AGGTGAAAGTAAGTG | 7415 |
rs751145794 | snp | A/C | 1.66128e-05 | 0.00288204 | intron-variant | VCP | GRCh38.p7 | 9:35062380 | AATGGAGACAATAAC[A/C]AAATGATAGTCTTTC | 7415 |
rs751227891 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | VCP | GRCh38.p7 | 9:35068354 | GTTGATAGGTCATCA[C/T]CTTTTGAACTAGAAG | 7415 |
rs751230057 | snp | A/G | 0.000131783 | 0.00811628 | synonymous-codon | VCP | GRCh38.p7 | 9:35062133 | CCGCTCCACCTCGCC[A/G]TGAGTCTGCCAGAAC | 7415 |
rs751290466 | in-del | -/T | 0.00207771 | 0.0321643 | frameshift-variant | VCP | GRCh38.p7 | 9:35059649 | CCAATGATGAACACA[-/T]TTTTTTTTTGTGGAC | 7415 |
rs751429960 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066947 | GGCTTTAGGCGAAGA[C/G]AGGAAGGAGAACAGG | 7415 |
rs751435398 | in-del | -/TAT | 1.65051e-05 | 0.00287267 | intron-variant | VCP | GRCh38.p7 | 9:35064323 | AGGAGAAGGCAAGAA[-/TAT]TATTATATCAGCAAA | 7415 |
rs751447557 | snp | C/T | | | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073021 | ATTAGTCTAGTCCTA[C/T]TGTGGTAACCCATAC | 7415 |
rs751610041 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | VCP | GRCh38.p7 | 9:35064216 | CCACCATCTCCTTTA[C/T]CTGAGCTAGCTGCTT | 7415 |
rs751616369 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074007 | CCAGTCCAGGAATTA[C/T]ATAGGAATGGTCACA | 7415 |
rs751710424 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074163 | TCAAGGAAGGCGTCA[C/T]GATCAGAGGGACGGA | 7415 |
rs751868966 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35062681 | CCAGTGATCAAAGTT[A/C]ATTTGCCCCAAACCC | 7415 |
rs751921549 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35068434 | CTAAAACTCATACTT[A/C]GGAAAGAAACAGTGA | 7415 |
rs751941022 | in-del | -/TC | | | intron-variant | VCP | GRCh38.p7 | 9:35065632 | AGAAGCCCATCAAGT[-/TC]TGACTTCTGCCATAT | 7415 |
rs751950418 | snp | C/T | 1.65729e-05 | 0.00287857 | intron-variant | VCP | GRCh38.p7 | 9:35061227 | CAAAGACCCAGCTGC[C/T]GCAGGAGGCTCAGAG | 7415 |
rs751952342 | snp | C/T | 1.65464e-05 | 0.00287627 | intron-variant | VCP | GRCh38.p7 | 9:35067881 | GTGAAGCCAAAAACC[C/T]CACACACACCTGATG | 7415 |
rs752007813 | snp | C/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056505 | ATGCCTTGGGAGTGG[C/T]GGGTAGCCCAAGGCT | 7415 |
rs752009669 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35069364 | CCTAGAAGCTAGGAT[A/C]ATTCACCAGACAGTG | 7415 |
rs752038734 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | VCP | GRCh38.p7 | 9:35066789 | CATGGATACGTTTGC[C/T]GTACTTCACATCAGG | 7415 |
rs752050289 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066428 | GATGGGGTTTCGCCA[C/T]GTTGGCCAGGCTGGT | 7415 |
rs752124708 | snp | C/T | 1.71387e-05 | 0.00292729 | intron-variant | VCP | GRCh38.p7 | 9:35066665 | CCTTAAGCTCAGAAT[C/T]AGCTCTCACCTTTCC | 7415 |
rs752338174 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35067301 | TGATCCTGGCCAGGT[G/T]ATGGTTGGTTGGGTA | 7415 |
rs752347349 | in-del | -/CCTCT | 1.67854e-05 | 0.00289697 | intron-variant | VCP | GRCh38.p7 | 9:35059254 | TACCTTAGCATTTAG[-/CCTCT]CCTCTCGAGATACGC | 7415 |
rs752382520 | snp | C/T | 4.9516e-05 | 0.00497549 | synonymous-codon | VCP | GRCh38.p7 | 9:35059547 | GGCAACACGGGACTT[C/T]TCATCAGGAAGTGGG | 7415 |
rs752466862 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | VCP | GRCh38.p7 | 9:35068370 | CTTTTGAACTAGAAG[A/G]AGGAAATGGAGTCAG | 7415 |
rs752479529 | snp | A/G | 2.6932e-05 | 0.00366951 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072361 | GAAGCCATGGCGCGC[A/G]CCTCTCCCGGCCGGC | 7415 |
rs752487557 | snp | C/T | 1.64991e-05 | 0.00287215 | intron-variant | VCP | GRCh38.p7 | 9:35057339 | TGTAGGTCCCCAAAG[C/T]AACTTAAGCACTGTC | 7415 |
rs752573338 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | VCP | GRCh38.p7 | 9:35060967 | GACTTATCAAGGGAG[A/G]GGTCAAAGCACGTAT | 7415 |
rs752679944 | snp | A/G | 1.65081e-05 | 0.00287293 | synonymous-codon | VCP | GRCh38.p7 | 9:35057128 | CCACTTAGCCATACA[A/G]GTCATCATCATTGTC | 7415 |
rs752765916 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | VCP | GRCh38.p7 | 9:35060824 | GCTCCTGTAGCTCAC[A/G]TTTGACATCCTCTAG | 7415 |
rs752936336 | snp | C/T | 1.65195e-05 | 0.00287393 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074435 | AGAGTGCAGTGGCCT[C/T]ATCCCTCCGATCTAG | 7415 |
rs752950954 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35057801 | GGCTAAGGAAACTTT[G/T]TGAGATAGTAGAAAT | 7415 |
rs753011642 | snp | C/T | 3.29495e-05 | 0.00405877 | synonymous-codon | VCP | GRCh38.p7 | 9:35059172 | CTCTGTCAGGTCAGC[C/T]CCAGAGAAGCCATTA | 7415 |
rs753084370 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35067282 | AAGAATCAAAAGCCT[C/G]AGATGATCCTGGCCA | 7415 |
rs753103789 | snp | C/G | 3.29506e-05 | 0.00405884 | synonymous-codon | VCP | GRCh38.p7 | 9:35062034 | TGGGTCAATGCTGTT[C/G]GGTCTGTTGGTTGCT | 7415 |
rs753147242 | snp | A/G | 4.94319e-05 | 0.00497127 | intron-variant | VCP | GRCh38.p7 | 9:35061007 | TGAGGCACGGGTGTG[A/G]TCCTTACCCGGAAGT | 7415 |
rs753189638 | snp | C/T | 1.65154e-05 | 0.00287358 | intron-variant | VCP | GRCh38.p7 | 9:35061732 | GGGCTCATCTCTAGT[C/T]CAGAGGTAAGAGACA | 7415 |
rs753221407 | snp | C/T | 1.65124e-05 | 0.00287331 | missense | VCP | GRCh38.p7 | 9:35067895 | CCCACACACACCTGA[C/T]GACATCCCCTAGGCG | 7415 |
rs753360809 | snp | C/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056198 | TATAGAGAATATCCA[C/T]CTGCAAGTAAGATTG | 7415 |
rs753411790 | snp | C/G | 3.29462e-05 | 0.00405857 | intron-variant | VCP | GRCh38.p7 | 9:35066832 | GCTGAGGATGACAAG[C/G]AGACTCCATATTACC | 7415 |
rs753415004 | in-del | -/C | 1.65877e-05 | 0.00287986 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057073 | CCCACCCCCAGGGAA[-/C]AAGGTCCAGGCAGGC | 7415 |
rs753417821 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35068196 | AGAAAAGAAACCTGG[A/G]AAAATCCCTCAAGTA | 7415 |
rs753523616 | snp | A/G | 1.67167e-05 | 0.00289103 | intron-variant | VCP | GRCh38.p7 | 9:35059841 | AGCACTAACAAAACT[A/G]GATGTCTCTAGGCAA | 7415 |
rs753528183 | snp | C/G/T | 3.29518e-05 | 0.00405894 | missense | VCP | GRCh38.p7 | 9:35060360 | ACTCCCCAAACCACA[C/G/T]GGTGAGCAGCTCAGG | 7415 |
rs753574871 | snp | A/C | 4.94214e-05 | 0.00497074 | intron-variant | VCP | GRCh38.p7 | 9:35064140 | GACTTGATTCCAGAG[A/C]CCAGGATGCTCACCT | 7415 |
rs753595390 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063151 | GGCTTGACTAGCGCT[C/G]CAGAGAGGGTGAGAA | 7415 |
rs753741558 | snp | A/T | 1.65397e-05 | 0.00287569 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074060 | AAGCCCTCCCCACAG[A/T]GAGACAGCCCACTGG | 7415 |
rs753820642 | snp | C/G | 3.30382e-05 | 0.00406423 | synonymous-codon | VCP | GRCh38.p7 | 9:35057474 | GCGCGCAAAGCGCAT[C/G]GCTTCTTCAAAGTGA | 7415 |
rs753827396 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063962 | ACAGACAATTTGATT[A/G]GCCTACTCTGGTTTT | 7415 |
rs753829387 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | VCP | GRCh38.p7 | 9:35068377 | ACTAGAAGGAGGAAA[C/T]GGAGTCAGTAGATAC | 7415 |
rs753920999 | snp | C/T | 4.94849e-05 | 0.00497393 | intron-variant | VCP | GRCh38.p7 | 9:35057364 | ACTGTCTAATGCTCC[C/T]AACCAACTTACCTGA | 7415 |
rs754013775 | snp | A/G | 1.64749e-05 | 0.00287005 | intron-variant | VCP | GRCh38.p7 | 9:35060981 | GGGGTCAAAGCACGT[A/G]TGTGTGTACCTGAGG | 7415 |
rs754125795 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35060029 | CCCAGCTACTCAGGA[G/T]GCTGAAGTAGGAGAA | 7415 |
rs754257860 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35058713 | CAGAAGTTGCAGTGA[A/G]CCAAGATCGTGCCAC | 7415 |
rs754258080 | snp | A/G | 1.65321e-05 | 0.00287502 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074444 | TGGCCTCATCCCTCC[A/G]ATCTAGCCTCTTCAG | 7415 |
rs754268174 | snp | C/T | 6.63779e-05 | 0.0057606 | missense | VCP | GRCh38.p7 | 9:35059501 | CACCTGCCTTGGCAA[C/T]TGGGGACTTGCGCAG | 7415 |
rs754299259 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | VCP | GRCh38.p7 | 9:35059191 | GAGAAGCCATTAGTC[A/G]TTTTAGCCAGGAACT | 7415 |
rs754618275 | snp | C/T | | | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074591 | TAGAGAGAGGAAGTA[C/T]CTTGCCTACACTCAC | 7415 |
rs754786759 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | VCP | GRCh38.p7 | 9:35068107 | TCATTGGGCTGACGG[A/G]GAGTAAGCAGCAGCC | 7415 |
rs754802166 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | VCP | GRCh38.p7 | 9:35067963 | ATCTTCTCATCAGAA[C/T]AAGTATCATCAGAAA | 7415 |
rs754918914 | snp | A/G | 1.73351e-05 | 0.00294402 | intron-variant | VCP | GRCh38.p7 | 9:35060565 | CAAGGCTACCTCCAC[A/G]TTTTGAAAGAAACCT | 7415 |
rs755080363 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | VCP | GRCh38.p7 | 9:35060421 | TTCATTAGCAATGGC[C/T]TTGGCCAACAAAGTT | 7415 |
rs755103525 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35058812 | AAACCTTGCTGTGTT[C/T]GCTGCACTCTCATAC | 7415 |
rs755163295 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35070160 | ACTGCCTCTAAACTA[A/G]TTTCTAACGACAGTT | 7415 |
rs755168304 | snp | G/T | 1.6473e-05 | 0.00286988 | synonymous-codon | VCP | GRCh38.p7 | 9:35064234 | GAGCTAGCTGCTTCC[G/T]GCAGCCACCAATGTC | 7415 |
rs755231576 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35057618 | CTGCAGTTTATTGGT[C/T]TCCTTGCCCTTCCAA | 7415 |
rs755275747 | snp | A/C/G | 6.59082e-05 | 0.00574026 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074164 | CAAGGAAGGCGTCAC[A/C/G]ATCAGAGGGACGGAT | 7415 |
rs755519450 | snp | A/G | 1.64795e-05 | 0.00287045 | missense | VCP | GRCh38.p7 | 9:35061017 | GTGTGGTCCTTACCC[A/G]GAAGTCATCCATAGT | 7415 |
rs755519508 | snp | A/C | 1.64727e-05 | 0.00286986 | missense | VCP | GRCh38.p7 | 9:35066811 | CACATCAGGGCATGG[A/C]TGGATGCTGAGGATG | 7415 |
rs755607327 | snp | C/G | 1.70316e-05 | 0.00291813 | intron-variant | VCP | GRCh38.p7 | 9:35066670 | AGCTCAGAATTAGCT[C/G]TCACCTTTCCGGATG | 7415 |
rs755625059 | snp | C/T | 9.90017e-05 | 0.00703499 | intron-variant | VCP | GRCh38.p7 | 9:35057226 | CCTGAAGGGAATCTG[C/T]GTACAAGAGCAAAGC | 7415 |
rs755641527 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35067141 | GGTCTTAAGCTAACA[A/C]TTGTCAGGGTCAGTG | 7415 |
rs755771885 | snp | A/C | 1.64789e-05 | 0.0028704 | synonymous-codon | VCP | GRCh38.p7 | 9:35063078 | CAGGATTCCTCTAGG[A/C]GGCTGTGGACCAATG | 7415 |
rs755848917 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35067838 | GGGTCCTGCCTGTAA[C/T]GCAGGCTATCTCTGG | 7415 |
rs756013193 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant | VCP | GRCh38.p7 | 9:35068372 | TTTGAACTAGAAGGA[A/G]GAAATGGAGTCAGTA | 7415 |
rs756047728 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35061874 | TCACTCTAGACAGGA[C/T]GTAGGGTAAAGGAAA | 7415 |
rs756067398 | in-del | -/T | 1.67281e-05 | 0.00289202 | intron-variant | VCP | GRCh38.p7 | 9:35067844 | GCCTGTAATGCAGGC[-/T]TATCTCTGGCCTCCC | 7415 |
rs756256106 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35072065 | CTAAGGGAGCCAATC[A/G]GGCGGGCCGGGGCCT | 7415 |
rs756444679 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | VCP | GRCh38.p7 | 9:35065222 | GAGTAATCATAAAAT[C/T]GGATACTGGAATCAG | 7415 |
rs756485118 | snp | A/G | 0.000248515 | 0.0111443 | synonymous-codon | VCP | GRCh38.p7 | 9:35059178 | CAGGTCAGCTCCAGA[A/G]AAGCCATTAGTCATT | 7415 |
rs756500825 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35057305 | CCTCTAGCTTCCTTA[C/G]GACTCCCATCCCTTT | 7415 |
rs756542501 | snp | A/G | 9.8956e-05 | 0.00703336 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074260 | GGTGAAAGATTGGCA[A/G]AAAGCTGGGCAGCCA | 7415 |
rs756573088 | snp | C/T | 1.64906e-05 | 0.00287142 | intron-variant | VCP | GRCh38.p7 | 9:35059053 | CATCTGGGGAAAGGA[C/T]GCAGACTCACCATGG | 7415 |
rs756632525 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074171 | GGCGTCACGATCAGA[A/G]GGACGGATCCAGCTC | 7415 |
rs756672952 | in-del | -/CAGGATTAGACATTGGGA | | | intron-variant | VCP | GRCh38.p7 | 9:35064081 | GCATGAAAACAGTCC[-/CAGGATTAGACATTGGGA]CAGGATTAGACATTG | 7415 |
rs756718766 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant | VCP | GRCh38.p7 | 9:35061550 | AGAGACACTGTAACG[C/T]CTGGTCAGCCATCAT | 7415 |
rs756789437 | snp | G/T | 1.65119e-05 | 0.00287327 | synonymous-codon | VCP | GRCh38.p7 | 9:35067896 | CCACACACACCTGAT[G/T]ACATCCCCTAGGCGT | 7415 |
rs756802978 | snp | A/G | 0.000115305 | 0.00759205 | intron-variant | VCP | GRCh38.p7 | 9:35066834 | TGAGGATGACAAGCA[A/G]ACTCCATATTACCAA | 7415 |
rs756976249 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35065650 | GACTTCTGCCATATA[C/G]GTAGCCCAAGTTTTC | 7415 |
rs756986992 | in-del | -/AG | 6.5912e-05 | 0.00574035 | intron-variant | VCP | GRCh38.p7 | 9:35065236 | TCGGATACTGGAATC[-/AG]GGAGAAAACTCACCT | 7415 |
rs757059299 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35068125 | GTAAGCAGCAGCCCT[A/G]GAGATTGGGATTCCC | 7415 |
rs757084197 | snp | C/T | 1.67503e-05 | 0.00289393 | intron-variant | VCP | GRCh38.p7 | 9:35059848 | ACAAAACTAGATGTC[C/T]CTAGGCAAACGTGGT | 7415 |
rs757119751 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35060651 | CCAGGTTCTCTAGAA[G/T]AAGACTCCTTAGTGC | 7415 |
rs757177035 | snp | C/G | | | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073030 | GTCCTATTGTGGTAA[C/G]CCATACACCCATCTT | 7415 |
rs757232381 | snp | A/G | 1.65422e-05 | 0.0028759 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074061 | AGCCCTCCCCACAGA[A/G]AGACAGCCCACTGGG | 7415 |
rs757257926 | in-del | -/AG | 1.64727e-05 | 0.00286986 | intron-variant | VCP | GRCh38.p7 | 9:35060771 | ACAATGTACTGAGAC[-/AG]TGACTCACCCTGGAC | 7415 |
rs757516574 | snp | C/T | 1.6495e-05 | 0.0028718 | missense | VCP | GRCh38.p7 | 9:35057161 | CTGTGTATACACTGC[C/T]ACCTGTGCCGCCTCC | 7415 |
rs757552913 | snp | A/G | 1.77729e-05 | 0.00298096 | intron-variant | VCP | GRCh38.p7 | 9:35066641 | GGTTTATTCCCTACA[A/G]TCAATAATCCTTAAG | 7415 |
rs757560700 | snp | A/G | 1.65512e-05 | 0.00287669 | intron-variant | VCP | GRCh38.p7 | 9:35065388 | AAATGTCTCCTGCGA[A/G]AGCAAACAGTACAAG | 7415 |
rs757636054 | snp | C/T | 4.96118e-05 | 0.0049803 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074448 | CTCATCCCTCCGATC[C/T]AGCCTCTTCAGAGTC | 7415 |
rs757680425 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35068456 | AAACAGTGAATAGAT[A/G]AAGCTGTCCCTAGAC | 7415 |
rs757712897 | snp | C/T | 3.30218e-05 | 0.00406323 | synonymous-codon | VCP | GRCh38.p7 | 9:35057126 | CACCACTTAGCCATA[C/T]AGGTCATCATCATTG | 7415 |
rs757728490 | snp | C/G/T | 4.94306e-05 | 0.00497124 | intron-variant | VCP | GRCh38.p7 | 9:35065241 | TACTGGAATCAGGGA[C/G/T]AAAACTCACCTCTCG | 7415 |
rs757802309 | snp | A/G | 1.64806e-05 | 0.00287054 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074324 | GGTCCAAGGACTCTA[A/G]GACACCAACTGCCCC | 7415 |
rs757829124 | snp | A/C | 1.64876e-05 | 0.00287116 | missense | VCP | GRCh38.p7 | 9:35059210 | TAGCCAGGAACTCCA[A/C]GTCCACATCCTAAAA | 7415 |
rs757918758 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | VCP | GRCh38.p7 | 9:35062111 | TCAACAACTGTGATA[C/T]AATGCGCCGCTCCAC | 7415 |
rs757942669 | snp | G/T | 1.65026e-05 | 0.00287246 | intron-variant | VCP | GRCh38.p7 | 9:35061961 | GAAGGAGAGAAGTAG[G/T]ACCTAAGCAAGGACG | 7415 |
rs757944833 | in-del | -/CTCATGC | 1.72274e-05 | 0.00293486 | intron-variant | VCP | GRCh38.p7 | 9:35059454 | GTACCAGCCTGAGGA[-/CTCATGC]AAGTCTCCCACAGCC | 7415 |