SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs758020657 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063394 | GGCCATTACACTAAG[C/G]GCTCAATTTTAGACA | 7415 |
rs758062750 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant | VCP | GRCh38.p7 | 9:35068097 | GGCCTTTGGGTCATT[A/G]GGCTGACGGGGAGTA | 7415 |
rs758065513 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071920 | GCCTCGGGCTCGCGG[A/G]GCCTGCTCTCTCCGG | 7415 |
rs758169026 | snp | C/T | 1.64931e-05 | 0.00287163 | missense | VCP | GRCh38.p7 | 9:35067909 | ATGACATCCCCTAGG[C/T]GTACACGAAGGTTAT | 7415 |
rs758189260 | snp | A/T | 0.000274763 | 0.0117178 | intron-variant | VCP | GRCh38.p7 | 9:35060560 | GGGTTCAAGGCTACC[A/T]CCACATTTTGAAAGA | 7415 |
rs758239334 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071420 | GTCAGAAAGCCCCAG[A/G]GCCCGGGTAATTTCT | 7415 |
rs758279219 | snp | A/G | 3.295e-05 | 0.00405881 | synonymous-codon | VCP | GRCh38.p7 | 9:35060403 | GATGAAGTTGGCCTG[A/G]CATTCATTAGCAATG | 7415 |
rs758367172 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | VCP | GRCh38.p7 | 9:35064169 | CTTCACACCAATTGC[C/T]TTAAAGAGGGCAGGA | 7415 |
rs758369238 | snp | C/T | 1.75182e-05 | 0.00295953 | intron-variant | VCP | GRCh38.p7 | 9:35060265 | AAAACAGCCTCTATT[C/T]CTTGCCCTCAGGCAA | 7415 |
rs758407400 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074158 | ATTCTTCAAGGAAGG[C/T]GTCACGATCAGAGGG | 7415 |
rs758455599 | snp | C/T | 1.65184e-05 | 0.00287384 | intron-variant | VCP | GRCh38.p7 | 9:35063113 | GTGTGATTAGGTTCC[C/T]ACCTTCTCCCAAACC | 7415 |
rs758565090 | snp | C/T | | | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35072867 | TTCTCAGCCAATCAA[C/T]GAAAGGAATAGGGCG | 7415 |
rs758575797 | snp | A/G | 1.6531e-05 | 0.00287493 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074076 | GAGACAGCCCACTGG[A/G]GACCCAGCTCAAGCT | 7415 |
rs758596783 | snp | A/C/G | 4.94567e-05 | 0.00497255 | synonymous-codon | VCP | GRCh38.p7 | 9:35057408 | CCGACTCTGCTGAAG[A/C/G]GTCTGGGCAAACATC | 7415 |
rs758602597 | snp | A/G | 3.31367e-05 | 0.00407029 | missense | VCP | GRCh38.p7 | 9:35057497 | CAAAGTGATCTCGAC[A/G]GATCTCAGGCACTGG | 7415 |
rs758694686 | snp | C/T | 1.64974e-05 | 0.00287201 | missense | VCP | GRCh38.p7 | 9:35061179 | GAGTCTCATTGGCTA[C/T]CTGCAGAGAAAGATC | 7415 |
rs758718803 | in-del | -/GA | 1.64749e-05 | 0.00287005 | intron-variant | VCP | GRCh38.p7 | 9:35068370 | CTTTTGAACTAGAAG[-/GA]GGAAATGGAGTCAGT | 7415 |
rs758842516 | snp | A/G | 6.97338e-05 | 0.00590441 | intron-variant | VCP | GRCh38.p7 | 9:35066655 | AGTCAATAATCCTTA[A/G]GCTCAGAATTAGCTC | 7415 |
rs758881387 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063881 | AAGAATGGCTTTTAT[A/G]TTCTAAGAGTTGTAA | 7415 |
rs758908163 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35067418 | TCCCAGGTCTGGCTC[C/T]AACTATTCCTCTCTC | 7415 |
rs758972118 | snp | C/T | 1.6563e-05 | 0.00287771 | intron-variant | VCP | GRCh38.p7 | 9:35065395 | TCCTGCGAGAGCAAA[C/T]AGTACAAGCACAGTT | 7415 |
rs758980894 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074111 | AAAACGTGGCAGCTA[C/T]AGGTCACAAGACTTT | 7415 |
rs759030803 | in-del | -/ATT | 6.60033e-05 | 0.00574433 | cds-indel | VCP | GRCh38.p7 | 9:35057138 | ATACAGGTCATCATC[-/ATT]GTCTTCTGTGTATAC | 7415 |
rs759096439 | in-del | AGGGGTTTTCTTTTTTTTTTTCCTGTGGGGATG/GATGGAGTTTCGCTTTTGTTGTCCAGGCT | | | intron-variant | VCP | GRCh38.p7 | 9:35069472 | TTTTTTTTTTTTTGA[lengthTooLong]GGAATGCAATGCTGC | 7415 |
rs759114510 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35069234 | TATCTGCAAAAGTAC[A/C]CAATTCCATAAAGTT | 7415 |
rs759122055 | snp | C/G | 1.64741e-05 | 0.00286998 | missense | VCP | GRCh38.p7 | 9:35063052 | TTTCCTGTTCCAGGA[C/G]GTCCGTAAAGCAGGA | 7415 |
rs759162490 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant | VCP | GRCh38.p7 | 9:35068365 | ATCACCTTTTGAACT[A/G]GAAGGAGGAAATGGA | 7415 |
rs759244351 | snp | A/G | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057027 | GAGCAGGCTGTGGGC[A/G]CACCCCTGGTCCCTC | 7415 |
rs759253669 | snp | A/G | 4.95323e-05 | 0.00497631 | intron-variant | VCP | GRCh38.p7 | 9:35057268 | GTTAGGACAGGGCCT[A/G]TGTAAGATTTCCACA | 7415 |
rs759353085 | snp | A/T | 1.66054e-05 | 0.00288139 | intron-variant | VCP | GRCh38.p7 | 9:35065416 | AAGCACAGTTAGAGG[A/T]GTCAACTACAAGACA | 7415 |
rs759473080 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35065167 | GCCACCGCAGCCGGC[C/T]GAGCACCCAGTCCTG | 7415 |
rs759475496 | snp | C/T | 0.000148245 | 0.00860815 | synonymous-codon | VCP | GRCh38.p7 | 9:35060807 | TTGCCCTACCTGGAC[C/T]AGCTCCTGTAGCTCA | 7415 |
rs759578203 | snp | A/C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066639 | AAGGTTTATTCCCTA[A/C/T]AGTCAATAATCCTTA | 7415 |
rs759587128 | snp | A/G | 1.67075e-05 | 0.00289023 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074537 | CTTAGAACTTGACAT[A/G]GTCTTAGGCATTGTT | 7415 |
rs759633658 | in-del | -/TCTATTT | | | intron-variant | VCP | GRCh38.p7 | 9:35063453 | TTTAAGAGAGCAGGG[-/TCTATTT]TCTTCATTGCCAGAG | 7415 |
rs759649712 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | VCP | GRCh38.p7 | 9:35059160 | ACGCTGGCAAATCTC[C/T]GTCAGGTCAGCTCCA | 7415 |
rs759650760 | in-del | -/AAG | | | intron-variant | VCP | GRCh38.p7 | 9:35057761 | TCAGTGATGGGGCTT[-/AAG]GAGGGGAGATGTTGA | 7415 |
rs759675304 | snp | A/G | 3.30136e-05 | 0.00406273 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074427 | CCTCCACCAGAGTGC[A/G]GTGGCCTCATCCCTC | 7415 |
rs759745417 | snp | A/G | | | synonymous-codon | VCP | GRCh38.p7 | 9:35060364 | CCCAAACCACATGGT[A/G]AGCAGCTCAGGACCC | 7415 |
rs759782318 | snp | A/G | | | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072606 | ACTCAAACGACGGTC[A/G]CAGACGCTTCGCTGA | 7415 |
rs759811779 | snp | C/T | 3.29603e-05 | 0.00405944 | intron-variant | VCP | GRCh38.p7 | 9:35061999 | AAGTATCTGGAGTCC[C/T]TACCAAATCGCCGTA | 7415 |
rs759899608 | snp | C/T | 1.65018e-05 | 0.00287239 | intron-variant | VCP | GRCh38.p7 | 9:35061720 | CAAACATAAACAGGG[C/T]TCATCTCTAGTCCAG | 7415 |
rs759966902 | in-del | -/A | 1.66085e-05 | 0.00288166 | intron-variant | VCP | GRCh38.p7 | 9:35062377 | CAGAATGGAGACAAT[-/A]ACAAAATGATAGTCT | 7415 |
rs759987483 | snp | A/C | 1.65395e-05 | 0.00287567 | intron-variant | VCP | GRCh38.p7 | 9:35067883 | GAAGCCAAAAACCCC[A/C]CACACACCTGATGAC | 7415 |
rs760031814 | snp | G/T | 1.6661e-05 | 0.00288621 | intron-variant | VCP | GRCh38.p7 | 9:35060530 | TCCACAGGATACTAG[G/T]AGGAAAAGGAAAGAG | 7415 |
rs760047414 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073812 | CACAAGCCTTCCCAC[A/G]CAAGTATATGTAGTA | 7415 |
rs760084336 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35062388 | CAATAACAAAATGAT[A/G]GTCTTTCCCAATTCC | 7415 |
rs760119711 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | VCP | GRCh38.p7 | 9:35064317 | TAAAGAAAGGAGAAG[A/G]CAAGAATATTATATC | 7415 |
rs760194948 | in-del | -/TAT | | | intron-variant | VCP | GRCh38.p7 | 9:35069897 | AAATTCATGAGTCTC[-/TAT]TATGTACCAGGCATT | 7415 |
rs760317486 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35071649 | AACTGGCTCAAACTT[C/T]CTAGTATGAACAACA | 7415 |
rs760337234 | snp | A/C/G | 3.29485e-05 | 0.00405874 | intron-variant | VCP | GRCh38.p7 | 9:35064138 | TAGACTTGATTCCAG[A/C/G]GCCCAGGATGCTCAC | 7415 |
rs760359166 | snp | C/G | | | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074123 | CTACAGGTCACAAGA[C/G]TTTGGCAGAGATGTC | 7415 |
rs760373249 | snp | C/T | 0.000668673 | 0.0182726 | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072376 | GCCTCTCCCGGCCGG[C/T]GGCTGTGGCGGCCCG | 7415 |
rs760411781 | snp | C/T | 1.6513e-05 | 0.00287336 | missense | VCP | GRCh38.p7 | 9:35057469 | GAACGGCGCGCAAAG[C/T]GCATGGCTTCTTCAA | 7415 |
rs760479906 | snp | C/G | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056429 | CAGGAGACATCATAC[C/G]GATGTTGATCAGGAG | 7415 |
rs760593200 | snp | A/G | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056920 | TACCAAATGAAAATC[A/G]CTTTTATTTTATCGC | 7415 |
rs760629776 | snp | A/G | 3.29951e-05 | 0.00406159 | intron-variant | VCP | GRCh38.p7 | 9:35057347 | CCCAAAGTAACTTAA[A/G]CACTGTCTAATGCTC | 7415 |
rs760711610 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35059021 | GGTGGCTGCTGCCTG[A/G]CTCTCCATGATTGGC | 7415 |
rs760755090 | snp | A/G | 1.64817e-05 | 0.00287064 | synonymous-codon | VCP | GRCh38.p7 | 9:35066727 | CTTAAGGTATACCTC[A/G]AAGAGATTACCAGTA | 7415 |
rs760756770 | snp | G/T | 3.29489e-05 | 0.00405874 | intron-variant | VCP | GRCh38.p7 | 9:35060968 | ACTTATCAAGGGAGG[G/T]GTCAAAGCACGTATG | 7415 |
rs760767588 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35063525 | TATCACACTGGAATG[C/T]TGTTCCTTACAATCA | 7415 |
rs760786829 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35060627 | ATGGTGTACCCAATG[A/G]TATCAGATCCAGGTT | 7415 |
rs760844719 | snp | A/C | 1.78723e-05 | 0.00298929 | intron-variant | VCP | GRCh38.p7 | 9:35066635 | TTCCAAGGTTTATTC[A/C]CTACAGTCAATAATC | 7415 |
rs760853796 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | VCP | GRCh38.p7 | 9:35059679 | CATGCCATCCATTTC[C/T]GTCAGGATCTGGTTG | 7415 |
rs761005679 | snp | C/T | 1.6525e-05 | 0.00287441 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074439 | TGCAGTGGCCTCATC[C/T]CTCCGATCTAGCCTC | 7415 |
rs761046932 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35059970 | AGACTTTGTCTCTAC[A/G]AAAAATAAAAAATTA | 7415 |
rs761051164 | snp | A/G | 1.64743e-05 | 0.00287 | missense | VCP | GRCh38.p7 | 9:35062068 | ATAACAATCACATGT[A/G]CCCTCTGCTTTAGGC | 7415 |
rs761138943 | snp | G/T | 1.64738e-05 | 0.00286995 | intron-variant | VCP | GRCh38.p7 | 9:35068078 | GCTGAGGAAAGAAAG[G/T]TAAGGCCTTTGGGTC | 7415 |
rs761165133 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35070993 | AATCCCTTTCCAGAA[C/T]TGCACAGGGGACTCC | 7415 |
rs761208219 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | VCP | GRCh38.p7 | 9:35068278 | CACCACACTGTTGTC[C/T]TCATTGATGGCTTCA | 7415 |
rs761430933 | snp | C/T | 0.000181185 | 0.00951628 | synonymous-codon | VCP | GRCh38.p7 | 9:35060876 | TACCTGTGGCACCTC[C/T]ACCACGGTTTCCCGC | 7415 |
rs761507411 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066976 | GGGTGGAAGTGAGGG[C/T]GAAGGAACAGCCCCA | 7415 |
rs761606019 | snp | C/G | 3.29478e-05 | 0.00405867 | intron-variant | VCP | GRCh38.p7 | 9:35064142 | CTTGATTCCAGAGCC[C/G]AGGATGCTCACCTTC | 7415 |
rs761685438 | snp | C/G | | | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055669 | ATTCCCTATTTTATC[C/G]TGTAGTGGCCTATGA | 7415 |
rs761695914 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074140 | TTGGCAGAGATGTCC[A/G]AAATTCTTCAAGGAA | 7415 |
rs761740384 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35067743 | AAACCTAAAGACAAC[A/C]CTGAAGCATAAGTCT | 7415 |
rs761773043 | snp | C/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056801 | GGCAGGTGGCAGTAG[C/T]GCCTTGGTTCACACC | 7415 |
rs761887444 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | VCP | GRCh38.p7 | 9:35066771 | TGTCATCAATGGGCA[A/G]CACATGGATACGTTT | 7415 |
rs761895823 | snp | C/T | 6.58892e-05 | 0.00573936 | missense | VCP | GRCh38.p7 | 9:35061609 | CATCTGCCAGCTTCA[C/T]GTTCTTGGTATGGAT | 7415 |
rs761952757 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35062747 | ATTCTAGCTTGCTCC[C/T]GCTCTGCAGTCTGTC | 7415 |
rs761954247 | snp | C/G | 1.67335e-05 | 0.00289248 | intron-variant | VCP | GRCh38.p7 | 9:35067842 | CCTGCCTGTAATGCA[C/G]GCTATCTCTGGCCTC | 7415 |
rs761986024 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon | VCP | GRCh38.p7 | 9:35061162 | AGCACCCACATGCCC[A/G]TGAGTCTCATTGGCT | 7415 |
rs762064655 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35065648 | CTGACTTCTGCCATA[G/T]AGGTAGCCCAAGTTT | 7415 |
rs762185724 | snp | C/T | 1.65633e-05 | 0.00287774 | missense | VCP | GRCh38.p7 | 9:35059512 | GCAACTGGGGACTTG[C/T]GCAGGTTAGCCTTGA | 7415 |
rs762247929 | snp | C/G | 1.64754e-05 | 0.00287009 | synonymous-codon | VCP | GRCh38.p7 | 9:35059748 | ACCTCCACGAGCCTT[C/G]GCAATCGAATCCAGC | 7415 |
rs762363538 | in-del | -/AC | 3.33244e-05 | 0.0040818 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074515 | GCCCCAGCCCAGAGT[-/AC]AGAGTCTTAGAACTT | 7415 |
rs762366254 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | VCP | GRCh38.p7 | 9:35063003 | GAAGAAGAAGGCTCC[A/G]GTCTCATTTGCTACA | 7415 |
rs762436337 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35059900 | CACTTTGGGAGGCCA[A/C]GGTGGGAGGATCACT | 7415 |
rs762469485 | snp | A/G | 1.65102e-05 | 0.00287312 | intron-variant | VCP | GRCh38.p7 | 9:35057258 | AAAAAAGAGGGTTAG[A/G]ACAGGGCCTGTGTAA | 7415 |
rs762491687 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35058528 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCACATCA | 7415 |
rs762559031 | snp | A/G | 0.000380621 | 0.0137901 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057102 | GCCAGCTCACTGCAC[A/G]CTGGCCACCACCACT | 7415 |
rs762562678 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35071792 | CTCCAAAAAGGCGGC[C/T]GTGAGCTTCCCTGAG | 7415 |
rs762651081 | in-del | -/T | | | intron-variant | VCP | GRCh38.p7 | 9:35062851 | TAACATACCCCAGCA[-/T]TAAGAAATATGCTAT | 7415 |
rs762659353 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon | VCP | GRCh38.p7 | 9:35065308 | TGGAGCAACAATGCA[A/G]TAAGGGCTAGGATCT | 7415 |
rs762714211 | in-del | -/GT | 4.94768e-05 | 0.00497352 | intron-variant | VCP | GRCh38.p7 | 9:35063098 | GTGGACCAATGCAGA[-/GT]GTGATTAGGTTCCCA | 7415 |
rs762761491 | snp | C/G | 1.64972e-05 | 0.00287199 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074411 | TAGTTTGGGCCTCCA[C/G]CCTCCACCAGAGTGC | 7415 |
rs762896399 | snp | C/T | 1.65176e-05 | 0.00287376 | intron-variant | VCP | GRCh38.p7 | 9:35064331 | GGCAAGAATATTATA[C/T]CAGCAAAAGCTGAGT | 7415 |
rs762952200 | snp | A/G | 1.6543e-05 | 0.00287597 | intron-variant | VCP | GRCh38.p7 | 9:35059028 | GCTGCCTGGCTCTCC[A/G]TGATTGGCACATCTG | 7415 |
rs763000489 | snp | C/G | 1.64866e-05 | 0.00287106 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074220 | AGGGGGAGAGACCTG[C/G]AGAGAAAGAAGGATG | 7415 |
rs763011046 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | VCP | GRCh38.p7 | 9:35059142 | GATGGCCAGCTTGCA[A/G]GCACGCTGGCAAATC | 7415 |
rs763044813 | snp | A/C | 1.74659e-05 | 0.0029551 | intron-variant | VCP | GRCh38.p7 | 9:35061712 | ACAGTACACAAACAT[A/C]AACAGGGCTCATCTC | 7415 |
rs763090963 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073890 | AACAGGAAAAAAGGT[G/T]CCTCGAGCAAAGTCA | 7415 |
rs763106348 | snp | G/T | 1.64822e-05 | 0.00287068 | intron-variant | VCP | GRCh38.p7 | 9:35061995 | TCAAAAGTATCTGGA[G/T]TCCTTACCAAATCGC | 7415 |
rs763209403 | snp | A/T | 1.66466e-05 | 0.00288496 | intron-variant | VCP | GRCh38.p7 | 9:35067861 | ATCTCTGGCCTCCCA[A/T]CCCTGTGAAGCCAAA | 7415 |
rs763298031 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | VCP | GRCh38.p7 | 9:35066784 | CAGCACATGGATACG[C/T]TTGCCGTACTTCACA | 7415 |
rs763524671 | snp | A/G | 1.68587e-05 | 0.00290329 | intron-variant | VCP | GRCh38.p7 | 9:35060297 | TCAATACATAGTTCA[A/G]CCTATTGTAGCTCAC | 7415 |
rs763534429 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35059921 | GAGGATCACTTGAGG[C/T]CAGAAATCCGAAACC | 7415 |
rs763590156 | snp | C/T | 3.29576e-05 | 0.00405928 | synonymous-codon | VCP | GRCh38.p7 | 9:35060340 | TTCTCTGACATTGGC[C/T]TCAGACTCCCCAAAC | 7415 |
rs763611715 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon | VCP | GRCh38.p7 | 9:35059763 | GGCAATCGAATCCAG[C/T]TCATCAAAGAATAGC | 7415 |
rs763622603 | in-del | -/AAAG | 1.64857e-05 | 0.00287099 | intron-variant | VCP | GRCh38.p7 | 9:35064303 | GAATATGGAGGAGAT[-/AAAG]AAAGGAGAAGGCAAG | 7415 |
rs763649722 | snp | A/T | 1.66829e-05 | 0.00288811 | intron-variant | VCP | GRCh38.p7 | 9:35060531 | CCACAGGATACTAGG[A/T]GGAAAAGGAAAGAGG | 7415 |
rs763691547 | in-del | -/GTT | | | intron-variant | VCP | GRCh38.p7 | 9:35071712 | GGGCTCGCCCTCTCC[-/GTT]CTAACAGTCCTTCAC | 7415 |
rs763798793 | in-del | -/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066069 | GGCGGAGGTTGCAGT[-/G]GAGCCGAGATTGCAC | 7415 |
rs763825181 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35065488 | CATTAGATAGTGCCC[C/T]TCATTAGATATTGCC | 7415 |
rs763851323 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35069936 | AGGGCTGGGGATACT[A/G]AAGTCAACAAAACAA | 7415 |
rs763852498 | snp | C/G | 1.64846e-05 | 0.0028709 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074127 | AGGTCACAAGACTTT[C/G]GCAGAGATGTCCGAA | 7415 |
rs763916932 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066871 | TTCGGGCCCAAGCAC[A/T]GGGTGTCCAAAAGGG | 7415 |
rs763920420 | snp | C/G | 3.29902e-05 | 0.00406128 | intron-variant | VCP | GRCh38.p7 | 9:35063098 | GTGGACCAATGCAGA[C/G]TGTGATTAGGTTCCC | 7415 |
rs763931139 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066622 | TGAGATAAAGATGTT[C/T]CAAGGTTTATTCCCT | 7415 |
rs763970537 | snp | C/T | 1.64972e-05 | 0.00287199 | intron-variant | VCP | GRCh38.p7 | 9:35057351 | AAGTAACTTAAGCAC[C/T]GTCTAATGCTCCCAA | 7415 |
rs763971546 | in-del | -/T | 0.00207771 | 0.0321643 | frameshift-variant | VCP | GRCh38.p7 | 9:35059650 | CCAATGATGAACACA[-/T]TTTTTTTTGTGGACA | 7415 |
rs764036918 | snp | A/G | 1.65141e-05 | 0.00287346 | missense | VCP | GRCh38.p7 | 9:35057470 | AACGGCGCGCAAAGC[A/G]CATGGCTTCTTCAAA | 7415 |
rs764162075 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon | VCP | GRCh38.p7 | 9:35061153 | TGCTAAGTCAGCACC[C/T]ACATGCCCGTGAGTC | 7415 |
rs764197648 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073910 | GAGCAAAGTCAATGA[C/G]TTGGTGGTGGCAGAG | 7415 |
rs764220345 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35062632 | GAGAGATGGCACACC[A/G]GATGGCACACCACTA | 7415 |
rs764224777 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063697 | ACACTTTCCCACTAG[A/G]AAAAGATTGAGAAGC | 7415 |
rs764251946 | snp | A/G | 8.2373e-05 | 0.00641714 | intron-variant | VCP | GRCh38.p7 | 9:35060979 | GAGGGGTCAAAGCAC[A/G]TATGTGTGTACCTGA | 7415 |
rs764339895 | snp | C/T | 5.34774e-05 | 0.00517067 | intron-variant | VCP | GRCh38.p7 | 9:35066637 | CCAAGGTTTATTCCC[C/T]ACAGTCAATAATCCT | 7415 |
rs764417368 | snp | C/T | 1.68012e-05 | 0.00289833 | intron-variant | VCP | GRCh38.p7 | 9:35059478 | GTCTCCCACAGCCCA[C/T]GATCTTGCACCTGCC | 7415 |
rs764429197 | snp | C/G | 0.000364528 | 0.0134956 | intron-variant | VCP | GRCh38.p7 | 9:35062357 | TCTCAGGACCTGAAA[C/G]GATACAGAATGGAGA | 7415 |
rs764460664 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35061247 | GAGGCTCAGAGACAA[C/T]AGAATCCTTCCCCTG | 7415 |
rs764519589 | snp | A/C | 1.6476e-05 | 0.00287014 | synonymous-codon | VCP | GRCh38.p7 | 9:35059187 | TCCAGAGAAGCCATT[A/C]GTCATTTTAGCCAGG | 7415 |
rs764572391 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35069249 | ACAATTCCATAAAGT[A/T]GGCTCAAAAAATCAA | 7415 |
rs764666776 | in-del | -/CATGATTGGCA | 1.65441e-05 | 0.00287607 | intron-variant | VCP | GRCh38.p7 | 9:35059027 | TGCTGCCTGGCTCTC[-/CATGATTGGCA]CATCTGGGGAAAGGA | 7415 |
rs764686985 | snp | C/G | 1.64738e-05 | 0.00286995 | synonymous-codon | VCP | GRCh38.p7 | 9:35062094 | TAGGCCATCCATGAG[C/G]GTCAACAACTGTGAT | 7415 |
rs764714590 | snp | C/T | 3.30044e-05 | 0.00406216 | synonymous-codon | VCP | GRCh38.p7 | 9:35067902 | ACACCTGATGACATC[C/T]CCTAGGCGTACACGA | 7415 |
rs764753926 | in-del | -/AATGATAGTCT | 0.000116307 | 0.00762496 | intron-variant | VCP | GRCh38.p7 | 9:35062382 | TGGAGACAATAACAA[-/AATGATAGTCT]TTCCCAATTCCTCCC | 7415 |
rs764776944 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | VCP | GRCh38.p7 | 9:35068087 | AGAAAGTTAAGGCCT[C/T]TGGGTCATTGGGCTG | 7415 |
rs764790678 | snp | A/G | 1.658e-05 | 0.00287919 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057083 | GGGAACAAGGTCCAG[A/G]CAGGCCAGCTCACTG | 7415 |
rs764950409 | snp | C/G | | | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074658 | CATCCCAGTGTCCAT[C/G]ATCTGCCCCCTACTC | 7415 |
rs765044616 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | VCP | GRCh38.p7 | 9:35064111 | GGACAGGATTAGACA[C/T]TGGCACCACTTTAGA | 7415 |
rs765061140 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | VCP | GRCh38.p7 | 9:35060390 | GACCCTTGATGGAGA[C/T]GAAGTTGGCCTGGCA | 7415 |
rs765086841 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon | VCP | GRCh38.p7 | 9:35064160 | GATGCTCACCTTCAC[A/G]CCAATTGCCTTAAAG | 7415 |
rs765086974 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074155 | GAAATTCTTCAAGGA[A/G]GGCGTCACGATCAGA | 7415 |
rs765140312 | snp | A/C | 0.000247441 | 0.0111202 | synonymous-codon | VCP | GRCh38.p7 | 9:35065362 | AGCACGCATCCCACC[A/C]CGGACAAGAAAAATG | 7415 |
rs765150956 | snp | G/T | 1.64838e-05 | 0.00287083 | splice-acceptor-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074218 | ACAGGGGGAGAGACC[G/T]GGAGAGAAAGAAGGA | 7415 |
rs765239601 | in-del | -/AAAA | | | intron-variant | VCP | GRCh38.p7 | 9:35061803 | CCTAATGCCAGCACT[-/AAAA]AAGTCTCAAGCTCTG | 7415 |
rs765384670 | snp | A/G | 1.65408e-05 | 0.00287578 | synonymous-codon | VCP | GRCh38.p7 | 9:35057486 | CATGGCTTCTTCAAA[A/G]TGATCTCGACGGATC | 7415 |
rs765387767 | snp | A/G | 8.23866e-05 | 0.00641767 | intron-variant | VCP | GRCh38.p7 | 9:35061000 | GTGTACCTGAGGCAC[A/G]GGTGTGGTCCTTACC | 7415 |
rs765420382 | snp | A/T | 1.64852e-05 | 0.00287094 | synonymous-codon | VCP | GRCh38.p7 | 9:35061165 | ACCCACATGCCCGTG[A/T]GTCTCATTGGCTACC | 7415 |
rs765474506 | snp | C/T | 1.76777e-05 | 0.00297297 | intron-variant | VCP | GRCh38.p7 | 9:35066646 | ATTCCCTACAGTCAA[C/T]AATCCTTAAGCTCAG | 7415 |
rs765596863 | snp | C/G/T | 3.2961e-05 | 0.00405951 | synonymous-codon | VCP | GRCh38.p7 | 9:35059754 | ACGAGCCTTGGCAAT[C/G/T]GAATCCAGCTCATCA | 7415 |
rs765603733 | snp | C/T | | | utr-variant-5-prime | VCP | GRCh38.p7 | 9:35072616 | CGGTCGCAGACGCTT[C/T]GCTGAGACTGAGCCG | 7415 |
rs765736779 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35068145 | TTGGGATTCCCAGTA[A/C]ACCCCACTCTATCTG | 7415 |
rs765795425 | snp | A/G | 1.65608e-05 | 0.00287752 | missense | VCP | GRCh38.p7 | 9:35059513 | CAACTGGGGACTTGC[A/G]CAGGTTAGCCTTGAG | 7415 |
rs765865935 | snp | C/G | 1.64732e-05 | 0.0028699 | synonymous-codon | VCP | GRCh38.p7 | 9:35063030 | TACAGCTCGAGCAAT[C/G]AGGGTCTTTCCTGTT | 7415 |
rs766042571 | snp | C/T | 0.000279999 | 0.0118288 | synonymous-codon | VCP | GRCh38.p7 | 9:35068326 | GGGACGGTTCTTCTG[C/T]TTGAGAATGGCTGTT | 7415 |
rs766048346 | snp | C/T | 0.00016547 | 0.00909437 | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35057103 | CCAGCTCACTGCACG[C/T]TGGCCACCACCACTT | 7415 |
rs766053871 | snp | C/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056942 | TTTTATCGCTTTTGT[C/T]TTGTATTTTTGCAAC | 7415 |
rs766130580 | snp | C/T | 6.59e-05 | 0.00573983 | intron-variant | VCP | GRCh38.p7 | 9:35068104 | GGGTCATTGGGCTGA[C/T]GGGGAGTAAGCAGCA | 7415 |
rs766140133 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | VCP | GRCh38.p7 | 9:35060792 | TCACCCTGGACCAAG[C/T]TGCCCTACCTGGACC | 7415 |
rs766228683 | snp | C/T | 0.000172164 | 0.00927645 | intron-variant | VCP | GRCh38.p7 | 9:35060561 | GGTTCAAGGCTACCT[C/T]CACATTTTGAAAGAA | 7415 |
rs766261105 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | VCP | GRCh38.p7 | 9:35065309 | GGAGCAACAATGCAA[C/T]AAGGGCTAGGATCTG | 7415 |
rs766296036 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063958 | CACAACAGACAATTT[A/G]ATTAGCCTACTCTGG | 7415 |
rs766323286 | snp | A/G | 4.94645e-05 | 0.00497291 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074233 | TGGAGAGAAAGAAGG[A/G]TGATGCCTAAGGGTG | 7415 |
rs766349187 | snp | C/T | 6.58935e-05 | 0.00573955 | synonymous-codon | VCP | GRCh38.p7 | 9:35063054 | TCCTGTTCCAGGAGG[C/T]CCGTAAAGCAGGATT | 7415 |
rs766357065 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071971 | GTGGTAGGCCGGACG[A/G]CAGACTGGCGCCCCA | 7415 |
rs766404812 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35062962 | AGCTAGACATAAGAT[A/G]AACCAAATATCTCAC | 7415 |
rs766524415 | snp | A/G | 3.29549e-05 | 0.00405911 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074159 | TTCTTCAAGGAAGGC[A/G]TCACGATCAGAGGGA | 7415 |
rs766622061 | snp | C/G | 1.65102e-05 | 0.00287312 | intron-variant | VCP | GRCh38.p7 | 9:35061194 | CCTGCAGAGAAAGAT[C/G]TACTTACTATGCTGC | 7415 |
rs766628725 | in-del | -/AAG | | | intron-variant | VCP | GRCh38.p7 | 9:35063191 | AACCCTGACAATATT[-/AAG]AATAAGCCCTCCGCA | 7415 |
rs766787045 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | VCP | GRCh38.p7 | 9:35066785 | AGCACATGGATACGT[C/T]TGCCGTACTTCACAT | 7415 |
rs766826293 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35063933 | TGTGTGTGTTTTGTG[C/T]GCACACGCACACAAC | 7415 |
rs767019331 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35067122 | ACCCAATATTACAAG[A/G]GAAGGTCTTAAGCTA | 7415 |
rs767026681 | snp | C/T | 0.000133871 | 0.00818032 | intron-variant | VCP | GRCh38.p7 | 9:35060302 | ACATAGTTCAGCCTA[C/T]TGTAGCTCACCTTGT | 7415 |
rs767081097 | snp | A/C | 2.9344e-05 | 0.00383029 | missense | VCP | GRCh38.p7 | 9:35072343 | CACACTCACTCGGCT[A/C]CAGAAGCCATGGCGC | 7415 |
rs767274225 | snp | A/G/T | 3.34718e-05 | 0.00409084 | intron-variant | VCP | GRCh38.p7 | 9:35067843 | CTGCCTGTAATGCAG[A/G/T]CTATCTCTGGCCTCC | 7415 |
rs767355870 | in-del | -/T | 1.79098e-05 | 0.00299242 | intron-variant | VCP | GRCh38.p7 | 9:35066631 | ATGTTCCAAGGTTTA[-/T]TTCCCTACAGTCAAT | 7415 |
rs767379602 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | VCP | GRCh38.p7 | 9:35060823 | AGCTCCTGTAGCTCA[C/T]GTTTGACATCCTCTA | 7415 |
rs767422036 | snp | A/G | 3.29473e-05 | 0.00405864 | intron-variant | VCP | GRCh38.p7 | 9:35060962 | GATGAGACTTATCAA[A/G]GGAGGGGTCAAAGCA | 7415 |
rs767565174 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35062750 | CTAGCTTGCTCCCGC[G/T]CTGCAGTCTGTCCAC | 7415 |
rs767586852 | snp | A/G | 1.66632e-05 | 0.0028864 | intron-variant | VCP | GRCh38.p7 | 9:35065431 | TGTCAACTACAAGAC[A/G]AAGTGAGAACTCATC | 7415 |
rs767625394 | in-del | -/TG | | | intron-variant | VCP | GRCh38.p7 | 9:35063915 | AAACCCATATATATA[-/TG]TGTGTGTGTGTTTTG | 7415 |
rs767655199 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063823 | TGCTCTAGACAGGCT[A/G]GCAAACTATGGTGAG | 7415 |
rs767762212 | snp | C/G | 1.64743e-05 | 0.00287 | missense | VCP | GRCh38.p7 | 9:35059165 | GGCAAATCTCTGTCA[C/G]GTCAGCTCCAGAGAA | 7415 |
rs767838037 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | VCP | GRCh38.p7 | 9:35068066 | CATCCATCTTGGGCT[A/G]AGGAAAGAAAGTTAA | 7415 |
rs767846588 | snp | C/T | 4.94328e-05 | 0.00497131 | synonymous-codon | VCP | GRCh38.p7 | 9:35062007 | GGAGTCCTTACCAAA[C/T]CGCCGTAGAGCTGGG | 7415 |
rs767850418 | snp | C/T | 1.65173e-05 | 0.00287374 | intron-variant | VCP | GRCh38.p7 | 9:35059042 | CATGATTGGCACATC[C/T]GGGGAAAGGATGCAG | 7415 |
rs768042101 | snp | G/T | 1.64754e-05 | 0.00287009 | synonymous-codon | VCP | GRCh38.p7 | 9:35065256 | GAAAACTCACCTCTC[G/T]TTTGATAGGCTCCCC | 7415 |
rs768082857 | snp | C/T | 3.30584e-05 | 0.00406548 | intron-variant | VCP | GRCh38.p7 | 9:35067888 | CAAAAACCCCACACA[C/T]ACCTGATGACATCCC | 7415 |
rs768117111 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35070950 | GGACACTCTTTGGGG[C/T]AATCCTCCATTGTCT | 7415 |
rs768235127 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074332 | GACTCTAGGACACCA[A/G]CTGCCCCTCAGCCCC | 7415 |
rs768235393 | in-del | -/AGA | | | intron-variant | VCP | GRCh38.p7 | 9:35060647 | AGATCCAGGTTCTCT[-/AGA]AGAAGACTCCTTAGT | 7415 |
rs768325047 | snp | A/G | 1.64817e-05 | 0.00287064 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074203 | AATAGCTTTCTAGGT[A/G]CAGGGGGAGAGACCT | 7415 |
rs768327051 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | VCP | GRCh38.p7 | 9:35060797 | CTGGACCAAGTTGCC[C/T]TACCTGGACCAGCTC | 7415 |
rs768333399 | snp | A/C | | | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074086 | ACTGGGGACCCAGCT[A/C]AAGCTCTTCAAAACG | 7415 |
rs768462341 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | VCP | GRCh38.p7 | 9:35059104 | TCTCGTTCTCGCCTA[A/G]TCTCACTCTCGATGG | 7415 |
rs768643940 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | VCP | GRCh38.p7 | 9:35061586 | CTTCACCTGTTCCAG[C/G]TCCACATCATCTGCC | 7415 |
rs768675930 | snp | C/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056750 | GGGGAAGGGAGGGCT[C/T]GGGCAGCATTGAGTC | 7415 |
rs768680373 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35068668 | GAAATGGAGGCTGAA[G/T]AGTTGTTAGAGAAAT | 7415 |
rs768698532 | snp | C/T | 1.74766e-05 | 0.00295601 | intron-variant | VCP | GRCh38.p7 | 9:35060270 | AGCCTCTATTCCTTG[C/T]CCTCAGGCAAATCAA | 7415 |
rs768733449 | snp | A/G | 3.29484e-05 | 0.00405871 | intron-variant | VCP | GRCh38.p7 | 9:35066866 | CACACTTCGGGCCCA[A/G]GCACTGGGTGTCCAA | 7415 |
rs768951162 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | VCP | GRCh38.p7 | 9:35059721 | AGCAGCCCCACCACC[A/G]TCTCCAATGTTACCT | 7415 |
rs769039060 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | VCP | GRCh38.p7 | 9:35062987 | TCTCACCATTGATCA[A/G]GAAGAAGAAGGCTCC | 7415 |
rs769080463 | snp | C/G | 3.30191e-05 | 0.00406306 | intron-variant | VCP | GRCh38.p7 | 9:35057242 | GTACAAGAGCAAAGC[C/G]AAAAAAGAGGGTTAG | 7415 |
rs769153776 | snp | A/C | 1.64868e-05 | 0.00287109 | missense | VCP | GRCh38.p7 | 9:35057416 | GCTGAAGGGTCTGGG[A/C]AAACATCTCATACTT | 7415 |
rs769205578 | snp | C/T | 3.29837e-05 | 0.00406088 | intron-variant | VCP | GRCh38.p7 | 9:35068410 | CTGCCCCAAGCGCCT[C/T]GCCAGTCTCTAAAAC | 7415 |
rs769279961 | snp | C/G | 1.64727e-05 | 0.00286986 | intron-variant | VCP | GRCh38.p7 | 9:35060927 | GCTCAAGGCCCACTA[C/G]AAAAGGAGGGAAAAC | 7415 |
rs769365847 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | VCP | GRCh38.p7 | 9:35060774 | ATGTACTGAGACAGT[A/G]ACTCACCCTGGACCA | 7415 |
rs769367929 | snp | A/G | 4.97146e-05 | 0.00498546 | intron-variant | VCP | GRCh38.p7 | 9:35065399 | GCGAGAGCAAACAGT[A/G]CAAGCACAGTTAGAG | 7415 |
rs769402626 | snp | C/T | | | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073205 | CCCCAATCCCACAGC[C/T]TTTGCAGTTTCTCAG | 7415 |
rs769455914 | snp | A/G | 0.000115322 | 0.00759261 | synonymous-codon | VCP | GRCh38.p7 | 9:35065275 | GATAGGCTCCCCTTC[A/G]CAGTGGATCACTGTG | 7415 |
rs769559260 | snp | A/C | 1.64765e-05 | 0.00287019 | intron-variant | VCP | GRCh38.p7 | 9:35062208 | CTATCCCCTCAGGTA[A/C]GCTCCTACTTTCTCT | 7415 |
rs769653404 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35060097 | GACTGTACCACTGCC[C/T]TCCAACCTGGGCAAC | 7415 |
rs769766010 | snp | A/C | 3.5269e-05 | 0.0041992 | intron-variant | VCP | GRCh38.p7 | 9:35066648 | TCCCTACAGTCAATA[A/C]TCCTTAAGCTCAGAA | 7415 |
rs769793706 | snp | C/G | 0.000364468 | 0.0134945 | missense | VCP | GRCh38.p7 | 9:35059132 | TGGATTCACGGATGG[C/G]CAGCTTGCAAGCACG | 7415 |
rs769800776 | snp | C/T | 3.29707e-05 | 0.00406008 | intron-variant | VCP | GRCh38.p7 | 9:35061989 | ACGGGGTCAAAAGTA[C/T]CTGGAGTCCTTACCA | 7415 |
rs769809827 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35070862 | CCTCTAATTCCCCAT[C/T]TACCTACTGAGATCA | 7415 |
rs770035800 | snp | A/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056702 | TAAACATCCAGCAAC[A/T]GTGGCCCCTACCCAC | 7415 |
rs770263417 | in-del | -/AAGT | 1.65957e-05 | 0.00288055 | frameshift-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074476 | GTCTGAAGCAGGTGA[-/AAGT]AAGTGTCTCGATTAC | 7415 |
rs770269183 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant | VCP | GRCh38.p7 | 9:35064289 | CTCTTCCTCATCCTG[A/G]ATATGGAGGAGATAA | 7415 |
rs770358873 | snp | A/T | 1.64749e-05 | 0.00287005 | intron-variant | VCP | GRCh38.p7 | 9:35064124 | CATTGGCACCACTTT[A/T]GACTTGATTCCAGAG | 7415 |
rs770393864 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063650 | ACCCACTAGGAAAAT[A/G]AGTAACTTCATCTTC | 7415 |
rs770427007 | snp | A/G | 1.64969e-05 | 0.00287196 | synonymous-codon | VCP | GRCh38.p7 | 9:35057450 | AATGTCATTGTCACT[A/G]ACAGAACGGCGCGCA | 7415 |
rs770449270 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35062472 | AAGGTGGTAACCTCT[A/G]CCTACTTCTCACATC | 7415 |
rs770455405 | snp | A/G | 4.95021e-05 | 0.0049748 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074101 | CAAGCTCTTCAAAAC[A/G]TGGCAGCTACAGGTC | 7415 |
rs770514866 | snp | G/T | 1.64781e-05 | 0.00287033 | missense | VCP | GRCh38.p7 | 9:35061047 | TAACTGCTAGAGAGT[G/T]CATGACCTCGGCATC | 7415 |
rs770545141 | snp | A/G | 0.000204144 | 0.010101 | intron-variant | VCP | GRCh38.p7 | 9:35072294 | TGCGCGGCTGGTCCC[A/G]GTGCGCGCCGCCGCA | 7415 |
rs770599017 | snp | C/G | 1.64727e-05 | 0.00286986 | intron-variant | VCP | GRCh38.p7 | 9:35060932 | AGGCCCACTAGAAAA[C/G]GAGGGAAAACTGGGG | 7415 |
rs770689315 | snp | G/T | 1.67461e-05 | 0.00289357 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074532 | AGAGTCTTAGAACTT[G/T]ACATAGTCTTAGGCA | 7415 |
rs770725781 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | VCP | GRCh38.p7 | 9:35059625 | AATGATGTCAGGCCG[A/G]TTGGTAGCGCCAATG | 7415 |
rs771114033 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35067539 | AATTAGACATACTAG[G/T]GAGAGTAGTGAGGAG | 7415 |
rs771167033 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35066486 | CCCGCCTCAGCCTCC[C/T]AAATTGCTGGGATTA | 7415 |
rs771308655 | snp | C/G | | | synonymous-codon | VCP | GRCh38.p7 | 9:35060918 | GTTACTCTGGCTCAA[C/G]GCCCACTAGAAAAGG | 7415 |
rs771374170 | snp | A/C | 1.64846e-05 | 0.0028709 | intron-variant | VCP | GRCh38.p7 | 9:35064299 | TCCTGAATATGGAGG[A/C]GATAAAGAAAGGAGA | 7415 |
rs771451437 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074183 | AGAGGGACGGATCCA[A/G]CTCAAATAGCTTTCT | 7415 |
rs771489734 | in-del | -/AG | 1.64741e-05 | 0.00286998 | intron-variant | VCP | GRCh38.p7 | 9:35062165 | GGATGTCTGGTCAGA[-/AG]TGAAGTCAGGGCCTT | 7415 |
rs771585685 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073707 | AAGTGAGGATTCCTG[G/T]AGCCCTTTCCTCATA | 7415 |
rs771589216 | snp | C/G | 1.64743e-05 | 0.00287 | intron-variant | VCP | GRCh38.p7 | 9:35064135 | CTTTAGACTTGATTC[C/G]AGAGCCCAGGATGCT | 7415 |
rs771662410 | snp | A/G | 1.65089e-05 | 0.00287301 | missense | VCP | GRCh38.p7 | 9:35057463 | CTGACAGAACGGCGC[A/G]CAAAGCGCATGGCTT | 7415 |
rs771669019 | snp | A/G | 4.94727e-05 | 0.00497332 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074112 | AAACGTGGCAGCTAC[A/G]GGTCACAAGACTTTG | 7415 |
rs771707534 | snp | A/G | 8.35415e-05 | 0.00646249 | intron-variant | VCP | GRCh38.p7 | 9:35057556 | TAAACACAGATCACT[A/G]GGGCTAGTTAAAGCC | 7415 |
rs771741211 | snp | C/G | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056187 | TTAAAAGAGAGTATA[C/G]AGAATATCCACCTGC | 7415 |
rs771751916 | snp | C/G | 4.94303e-05 | 0.00497119 | missense | VCP | GRCh38.p7 | 9:35061080 | TGGTCTCATCCTCTA[C/G]GTCAATGAGATCCAT | 7415 |
rs771801561 | snp | C/G | 1.64732e-05 | 0.0028699 | intron-variant | VCP | GRCh38.p7 | 9:35061558 | TGTAACGCCTGGTCA[C/G]CCATCATCATCACTT | 7415 |
rs772069942 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon | VCP | GRCh38.p7 | 9:35066721 | GTACGGCTTAAGGTA[C/T]ACCTCGAAGAGATTA | 7415 |
rs772075813 | snp | A/T | | | intron-variant | VCP | GRCh38.p7 | 9:35070455 | TTTTTATTTTTTGAA[A/T]CGGAGTCTCCCTCTG | 7415 |
rs772137901 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | VCP | GRCh38.p7 | 9:35059643 | GGTAGCGCCAATGAT[A/G]AACACATTTTTTTTT | 7415 |
rs772163720 | snp | C/T | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056862 | ACAACAGAAATGGCA[C/T]AGGCCCAAGGCCCAA | 7415 |
rs772202013 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | VCP | GRCh38.p7 | 9:35068400 | GTAGATACTCCTGCC[C/T]CAAGCGCCTCGCCAG | 7415 |
rs772228010 | snp | C/G | 1.6473e-05 | 0.00286988 | intron-variant | VCP | GRCh38.p7 | 9:35062966 | AGACATAAGATGAAC[C/G]AAATATCTCACCATT | 7415 |
rs772315780 | snp | C/G | 1.65258e-05 | 0.00287448 | missense | VCP | GRCh38.p7 | 9:35062310 | GGCTTTACGAAGGTT[C/G]CTCTCAGACTCACCA | 7415 |
rs772361067 | in-del | -/TT | | | intron-variant | VCP | GRCh38.p7 | 9:35069454 | TCTCCCTTTTTTTTT[-/TT]TTTTTTTTTTTTTTG | 7415 |
rs772450349 | snp | C/G | | | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074461 | TCTAGCCTCTTCAGA[C/G]TCTGAAGCAGGTGAA | 7415 |
rs772450666 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071812 | GCTTCCCTGAGCTCG[A/G]CGGGCCTTCCCCGAC | 7415 |
rs772558871 | snp | C/T | 1.64955e-05 | 0.00287184 | missense | VCP | GRCh38.p7 | 9:35057205 | GGGCCAGCTCCACCC[C/T]GGTTCCCTGAAGGGA | 7415 |
rs772569728 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | VCP | GRCh38.p7 | 9:35060889 | TCTACCACGGTTTCC[C/T]GCAGTGCTGATGGGT | 7415 |
rs772582018 | in-del | -/AA | | | intron-variant | VCP | GRCh38.p7 | 9:35060130 | GCCAGACCCTGTCTC[-/AA]AAGAGAGAGAGAGAG | 7415 |
rs772637049 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071413 | AGGTGGGGTCAGAAA[A/G]CCCCAGAGCCCGGGT | 7415 |
rs772733434 | snp | A/G | 1.65086e-05 | 0.00287298 | intron-variant | VCP | GRCh38.p7 | 9:35057244 | ACAAGAGCAAAGCCA[A/G]AAAAGAGGGTTAGGA | 7415 |
rs772756435 | snp | A/C | 1.6473e-05 | 0.00286988 | intron-variant | VCP | GRCh38.p7 | 9:35060928 | CTCAAGGCCCACTAG[A/C]AAAGGAGGGAAAACT | 7415 |
rs772777679 | snp | G/T | 1.64727e-05 | 0.00286986 | synonymous-codon | VCP | GRCh38.p7 | 9:35068311 | AACAATTAACCGATT[G/T]GGACGGTTCTTCTGT | 7415 |
rs772793628 | snp | A/G | 1.66156e-05 | 0.00288228 | intron-variant | VCP | GRCh38.p7 | 9:35067868 | GCCTCCCATCCCTGT[A/G]AAGCCAAAAACCCCA | 7415 |
rs772832262 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35070588 | ACAGGTGTGCACCAT[C/T]ACCATGCCTGGCTAC | 7415 |
rs772844322 | snp | A/C | 1.65759e-05 | 0.00287883 | intron-variant | VCP | GRCh38.p7 | 9:35065400 | CGAGAGCAAACAGTA[A/C]AAGCACAGTTAGAGG | 7415 |
rs772930867 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | VCP | GRCh38.p7 | 9:35065293 | GTGGATCACTGTGTC[C/T]GGAGCAACAATGCAA | 7415 |
rs772995473 | snp | A/G | 1.64863e-05 | 0.00287104 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074219 | CAGGGGGAGAGACCT[A/G]GAGAGAAAGAAGGAT | 7415 |
rs773083883 | snp | C/T | 1.64871e-05 | 0.00287111 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074391 | AGCATCTTCATGTGA[C/T]CCCTTAGTTTGGGCC | 7415 |
rs773115735 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | VCP | GRCh38.p7 | 9:35061994 | GTCAAAAGTATCTGG[A/G]GTCCTTACCAAATCG | 7415 |
rs773253809 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063852 | AGATTTGTTTTTACA[A/G]GGTCCATTGATACAA | 7415 |
rs773283632 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | VCP | GRCh38.p7 | 9:35059139 | ACGGATGGCCAGCTT[A/G]CAAGCACGCTGGCAA | 7415 |
rs773319803 | snp | A/T | 1.64732e-05 | 0.0028699 | missense | VCP | GRCh38.p7 | 9:35067995 | GACGATGCAAACAGC[A/T]TCTCGTCTCTTCTTT | 7415 |
rs773346865 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35062615 | ACCTCTGGCTAGAGC[A/G]AGAGAGATGGCACAC | 7415 |
rs773353123 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35057987 | ACCACATTTGGATTA[C/T]ATCCTACCTAGCGGT | 7415 |
rs773360549 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35068585 | CGTCAGTGTCCCAGC[G/T]ATAAGGCCCCAAGTG | 7415 |
rs773373275 | snp | A/C | 1.67441e-05 | 0.0028934 | intron-variant | VCP | GRCh38.p7 | 9:35057576 | TAGTTAAAGCCCAGC[A/C]TGGATTTCATCCCAG | 7415 |
rs773487313 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35064740 | ATTTCAATCACTTAT[A/G]TATTTTGGGTTCAGT | 7415 |
rs773670816 | in-del | -/AGG | 1.65057e-05 | 0.00287273 | intron-variant | VCP | GRCh38.p7 | 9:35061958 | ATGAAGGAGAGAAGT[-/AGG]AGGACCTAAGCAAGG | 7415 |
rs773673950 | snp | C/T | 3.29755e-05 | 0.00406038 | missense | VCP | GRCh38.p7 | 9:35060484 | TCCCTTGGAAGGTGT[C/T]ATGCCAAACTTCAGG | 7415 |
rs773682510 | snp | C/T | | | synonymous-codon | VCP | GRCh38.p7 | 9:35060852 | TAGGCCCCCGATGTC[C/T]TCCCAGGTTACCTGT | 7415 |
rs773844815 | snp | A/G | 1.64977e-05 | 0.00287203 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074104 | GCTCTTCAAAACGTG[A/G]CAGCTACAGGTCACA | 7415 |
rs773849967 | snp | G/T | 3.29484e-05 | 0.00405871 | intron-variant | VCP | GRCh38.p7 | 9:35064130 | CACCACTTTAGACTT[G/T]ATTCCAGAGCCCAGG | 7415 |
rs773881101 | snp | A/G | 3.29554e-05 | 0.00405914 | synonymous-codon | VCP | GRCh38.p7 | 9:35061066 | GACCTCGGCATCAAT[A/G]GTCTCATCCTCTAGG | 7415 |
rs773886647 | in-del | -/A | | | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073187 | ACTGCACCCTCTGGT[-/A]AACCCCAATCCCACA | 7415 |
rs773912640 | snp | C/T | 1.65086e-05 | 0.00287298 | missense | VCP | GRCh38.p7 | 9:35057460 | TCACTGACAGAACGG[C/T]GCGCAAAGCGCATGG | 7415 |
rs773939501 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | VCP | GRCh38.p7 | 9:35063042 | AATCAGGGTCTTTCC[C/T]GTTCCAGGAGGTCCG | 7415 |
rs774000000 | snp | G/T | 1.65097e-05 | 0.00287308 | intron-variant | VCP | GRCh38.p7 | 9:35057263 | AGAGGGTTAGGACAG[G/T]GCCTGTGTAAGATTT | 7415 |
rs774241933 | snp | A/G | 1.66012e-05 | 0.00288103 | intron-variant | VCP | GRCh38.p7 | 9:35065413 | TACAAGCACAGTTAG[A/G]GGTGTCAACTACAAG | 7415 |
rs774362761 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35065450 | TGAGAACTCATCAGA[C/T]CCTGGGGTCAAAATG | 7415 |
rs774426027 | snp | C/T | 3.34001e-05 | 0.00408643 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074536 | TCTTAGAACTTGACA[C/T]AGTCTTAGGCATTGT | 7415 |
rs774493514 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35068832 | GTCCTCCTCTATAAA[A/G]GAAGGAATATAATAC | 7415 |
rs774502636 | snp | A/C | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056767 | GGCAGCATTGAGTCA[A/C]GTGCAGATGCTTTAC | 7415 |
rs774541798 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | VCP | GRCh38.p7 | 9:35059157 | AGCACGCTGGCAAAT[C/T]TCTGTCAGGTCAGCT | 7415 |
rs774553416 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | VCP | GRCh38.p7 | 9:35068231 | CAGTAAGGAAAGACT[A/G]GTCTGTGGCCACAGC | 7415 |
rs774553460 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant | VCP | GRCh38.p7 | 9:35061998 | AAAGTATCTGGAGTC[C/T]TTACCAAATCGCCGT | 7415 |
rs774581194 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063806 | CTTCTACTGGGTGAC[A/G]TTGCTCTAGACAGGC | 7415 |
rs774641311 | snp | A/G | 1.64727e-05 | 0.00286986 | stop-gained | VCP | GRCh38.p7 | 9:35068036 | ACACTGTGTCACCTC[A/G]GAACAACTGCAATTC | 7415 |
rs774727730 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35064574 | GGCCTCAAAGAACAA[C/G]TACAAAAATCCCAAG | 7415 |
rs774809989 | in-del | -/AAG | 1.64732e-05 | 0.0028699 | cds-indel | VCP | GRCh38.p7 | 9:35062986 | ATCTCACCATTGATC[-/AAG]AAGAAGAAGGCTCCA | 7415 |
rs774905848 | snp | A/T | 3.29484e-05 | 0.00405871 | intron-variant | VCP | GRCh38.p7 | 9:35064136 | TTTAGACTTGATTCC[A/T]GAGCCCAGGATGCTC | 7415 |
rs774960345 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35058487 | TCAGCTCAAAACCTT[G/T]CTCTGTGGTTCACGC | 7415 |
rs774962081 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071779 | CCCGCCGACCCGGCT[C/G]CAAAAAGGCGGCTGT | 7415 |
rs775000011 | snp | A/G | 1.64887e-05 | 0.00287125 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074117 | TGGCAGCTACAGGTC[A/G]CAAGACTTTGGCAGA | 7415 |
rs775006879 | snp | C/T | 1.65277e-05 | 0.00287464 | synonymous-codon | VCP | GRCh38.p7 | 9:35060514 | GAATTTGTCTGGGTG[C/T]TCCACAGGATACTAG | 7415 |
rs775015391 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35070731 | CTGAGCCACTGTGCC[C/G]GGTCAATAGTTTGTA | 7415 |
rs775017935 | snp | A/G | 4.94996e-05 | 0.00497467 | intron-variant | VCP | GRCh38.p7 | 9:35064316 | ATAAAGAAAGGAGAA[A/G]GCAAGAATATTATAT | 7415 |
rs775020335 | snp | G/T | 5.01249e-05 | 0.00500599 | intron-variant | VCP | GRCh38.p7 | 9:35057557 | AAACACAGATCACTA[G/T]GGCTAGTTAAAGCCC | 7415 |
rs775092396 | snp | A/G | 1.67069e-05 | 0.00289019 | intron-variant | VCP | GRCh38.p7 | 9:35060304 | ATAGTTCAGCCTATT[A/G]TAGCTCACCTTGTCA | 7415 |
rs775105790 | in-del | -/CAGAGTA | 1.6646e-05 | 0.00288491 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074509 | CCTGTAGCCCCAGCC[-/CAGAGTA]CAGAGTCTTAGAACT | 7415 |
rs775113723 | snp | G/T | 1.648e-05 | 0.0028705 | missense, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074195 | CCAGCTCAAATAGCT[G/T]TCTAGGTACAGGGGG | 7415 |
rs775191293 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35059819 | GTAGGAGGAATGGAT[G/T]GATTCAAGCACTAAC | 7415 |
rs775316749 | snp | A/G | 1.65113e-05 | 0.00287322 | synonymous-codon | VCP | GRCh38.p7 | 9:35057468 | AGAACGGCGCGCAAA[A/G]CGCATGGCTTCTTCA | 7415 |
rs775348132 | snp | A/G | 0.000148252 | 0.00860837 | synonymous-codon | VCP | GRCh38.p7 | 9:35066775 | ATCAATGGGCAGCAC[A/G]TGGATACGTTTGCCG | 7415 |
rs775408796 | snp | C/G | 3.29761e-05 | 0.00406041 | missense | VCP | GRCh38.p7 | 9:35061118 | CGGATGGCTTGCAGA[C/G]CAGCCTCTGAGCACA | 7415 |
rs775567003 | snp | A/C | 1.64874e-05 | 0.00287113 | missense | VCP | GRCh38.p7 | 9:35066723 | ACGGCTTAAGGTATA[A/C]CTCGAAGAGATTACC | 7415 |
rs775606754 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | VCP | GRCh38.p7 | 9:35059659 | AACACATTTTTTTTT[C/G]TGGACATGCCATCCA | 7415 |
rs775655244 | snp | C/T | 1.78979e-05 | 0.00299143 | intron-variant | VCP | GRCh38.p7 | 9:35066634 | GTTCCAAGGTTTATT[C/T]CCTACAGTCAATAAT | 7415 |
rs775672980 | snp | A/C | 1.65425e-05 | 0.00287593 | synonymous-codon | VCP | GRCh38.p7 | 9:35062322 | GTTGCTCTCAGACTC[A/C]CCAGCCAATTTGCTC | 7415 |
rs775760970 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | VCP | GRCh38.p7 | 9:35068260 | GCTTACCTGGGACAA[A/G]GACACCACACTGTTG | 7415 |
rs775948048 | snp | C/T | 1.6937e-05 | 0.00291002 | missense | VCP | GRCh38.p7 | 9:35066675 | AGAATTAGCTCTCAC[C/T]TTTCCGGATGGGTCG | 7415 |
rs775975307 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35069199 | AAAGAGGCTCAAGGT[C/T]AAAAGGAACTTCACA | 7415 |
rs776054562 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant | VCP | GRCh38.p7 | 9:35068076 | GGGCTGAGGAAAGAA[A/G]GTTAAGGCCTTTGGG | 7415 |
rs776057031 | snp | A/C/G | 3.35448e-05 | 0.0040953 | intron-variant | VCP | GRCh38.p7 | 9:35060539 | TACTAGGAGGAAAAG[A/C/G]AAAGAGGGTTCAAGG | 7415 |
rs776154559 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | VCP | GRCh38.p7 | 9:35065258 | AAACTCACCTCTCGT[C/T]TGATAGGCTCCCCTT | 7415 |
rs776155081 | snp | A/G | 3.29468e-05 | 0.00405861 | intron-variant | VCP | GRCh38.p7 | 9:35060766 | CAATTACAATGTACT[A/G]AGACAGTGACTCACC | 7415 |
rs776205250 | snp | A/C | | | downstream-variant-500B, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35073525 | TTAGGAAGGGAGTGA[A/C]GAGTTACTCTGAGAG | 7415 |
rs776337442 | snp | C/T | 3.29641e-05 | 0.00405968 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074204 | ATAGCTTTCTAGGTA[C/T]AGGGGGAGAGACCTG | 7415 |
rs776513109 | snp | C/G | 1.64746e-05 | 0.00287002 | intron-variant | VCP | GRCh38.p7 | 9:35066867 | ACACTTCGGGCCCAA[C/G]CACTGGGTGTCCAAA | 7415 |
rs776673109 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35066495 | GCCTCCCAAATTGCT[A/G]GGATTATAGGTGTGA | 7415 |
rs776702699 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon | VCP | GRCh38.p7 | 9:35061592 | CTGTTCCAGGTCCAC[A/G]TCATCTGCCAGCTTC | 7415 |
rs776726125 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35065149 | CTGGGATTACAGGTG[C/T]CAGCCACCGCAGCCG | 7415 |
rs776786033 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35065570 | GAGAAAGGTAAACTG[C/T]GAAGAGTCCCTCTGA | 7415 |
rs776790779 | snp | A/C | 3.29658e-05 | 0.00405978 | synonymous-codon | VCP | GRCh38.p7 | 9:35061159 | GTCAGCACCCACATG[A/C]CCGTGAGTCTCATTG | 7415 |
rs776808332 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | VCP | GRCh38.p7 | 9:35059728 | CCACCACCATCTCCA[A/G]TGTTACCTCCACGAG | 7415 |
rs776815786 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | VCP | GRCh38.p7 | 9:35066765 | CCACTGTGTCATCAA[C/T]GGGCAGCACATGGAT | 7415 |
rs776897082 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | VCP | GRCh38.p7 | 9:35063000 | CAAGAAGAAGAAGGC[C/T]CCAGTCTCATTTGCT | 7415 |
rs776916347 | snp | C/T | 1.74546e-05 | 0.00295415 | intron-variant | VCP | GRCh38.p7 | 9:35060271 | GCCTCTATTCCTTGC[C/T]CTCAGGCAAATCAAT | 7415 |
rs776937138 | in-del | -/GACGGATCCA | 6.59082e-05 | 0.00574019 | frameshift-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074173 | CGTCACGATCAGAGG[-/GACGGATCCA]GCTCAAATAGCTTTC | 7415 |
rs777107534 | snp | A/C | 3.29457e-05 | 0.00405854 | intron-variant | VCP | GRCh38.p7 | 9:35066821 | CATGGCTGGATGCTG[A/C]GGATGACAAGCAGAC | 7415 |
rs777133346 | in-del | -/CTATCC | 1.64746e-05 | 0.00287002 | intron-variant | VCP | GRCh38.p7 | 9:35062192 | CCTTTCAACCCCCCT[-/CTATCC]CTATCCCCTCAGGTA | 7415 |
rs777179882 | snp | C/T | 3.31807e-05 | 0.00407299 | intron-variant | VCP | GRCh38.p7 | 9:35062367 | TGAAAGGATACAGAA[C/T]GGAGACAATAACAAA | 7415 |
rs777223220 | snp | A/C | 1.64776e-05 | 0.00287028 | missense | VCP | GRCh38.p7 | 9:35061019 | GTGGTCCTTACCCGG[A/C]AGTCATCCATAGTAA | 7415 |
rs777277316 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | VCP | GRCh38.p7 | 9:35068411 | TGCCCCAAGCGCCTC[A/G]CCAGTCTCTAAAACT | 7415 |
rs777292314 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063612 | TAAACTGTCCACATA[C/G]AAAATGAAATTATTT | 7415 |
rs777331985 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35064350 | CAAAAGCTGAGTTTC[C/T]CTAAATCATTCCACT | 7415 |
rs777336987 | snp | A/G | | | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074702 | AACAGCAGAGTCATG[A/G]TCTTTGTGTCTGAGG | 7415 |
rs777365150 | snp | C/T | 0.000117097 | 0.0076508 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074524 | CAGAGTACAGAGTCT[C/T]AGAACTTGACATAGT | 7415 |
rs777402266 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | VCP | GRCh38.p7 | 9:35059610 | GAGGATGGCAGGATC[A/G]ATGATGTCAGGCCGG | 7415 |
rs777487177 | snp | A/T | 1.64732e-05 | 0.0028699 | intron-variant | VCP | GRCh38.p7 | 9:35062944 | CAGTTCAAAATTGGG[A/T]CTAGCTAGACATAAG | 7415 |
rs777504055 | snp | A/G | 1.66746e-05 | 0.00288739 | intron-variant | VCP | GRCh38.p7 | 9:35059837 | TTCAAGCACTAACAA[A/G]ACTAGATGTCTCTAG | 7415 |
rs777700993 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | VCP | GRCh38.p7 | 9:35068373 | TTGAACTAGAAGGAG[A/G]AAATGGAGTCAGTAG | 7415 |
rs777730052 | snp | C/T | | | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35072967 | GGCTCCGGAGTTTAT[C/T]CTCCTGGAAGAACGT | 7415 |
rs777769657 | snp | G/T | 1.64808e-05 | 0.00287057 | synonymous-codon | VCP | GRCh38.p7 | 9:35062225 | CTCCTACTTTCTCTC[G/T]TTTGGGAGCGATGGC | 7415 |
rs777805553 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35072125 | CCGACCCGGACCCAA[C/T]GCAAGCCCCGCCTAG | 7415 |
rs777846897 | in-del | -/G | 1.64746e-05 | 0.00287002 | intron-variant | VCP | GRCh38.p7 | 9:35068372 | TTTGAACTAGAAGGA[-/G]GAAATGGAGTCAGTA | 7415 |
rs777887584 | snp | A/G | 1.64985e-05 | 0.0028721 | synonymous-codon | VCP | GRCh38.p7 | 9:35057150 | ATCATTGTCTTCTGT[A/G]TATACACTGCCACCT | 7415 |
rs778014590 | snp | G/T | | | intron-variant | VCP | GRCh38.p7 | 9:35059005 | AACTCCAGGGCATGG[G/T]GGTGGCTGCTGCCTG | 7415 |
rs778031057 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071045 | GCTAAGAGTCATCAA[A/G]GTGACCAAGAGGTTA | 7415 |
rs778069672 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | VCP | GRCh38.p7 | 9:35060846 | ATCCTCTAGGCCCCC[A/G]ATGTCTTCCCAGGTT | 7415 |
rs778121223 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35065987 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGACGCCT | 7415 |
rs778155449 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | VCP | GRCh38.p7 | 9:35060750 | CTGAGATCACCCAGA[C/T]CAATTACAATGTACT | 7415 |
rs778260698 | snp | C/T | | | downstream-variant-500B | VCP | GRCh38.p7 | 9:35055868 | TATTTTATTCAAAAT[C/T]ACGGTGTTCAGGACT | 7415 |
rs778331428 | snp | A/G | 8.24056e-05 | 0.00641841 | intron-variant | VCP | GRCh38.p7 | 9:35064295 | CTCATCCTGAATATG[A/G]AGGAGATAAAGAAAG | 7415 |
rs778414106 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35063206 | AAGAATAAGCCCTCC[A/G]CAGTAAATGCTAAGA | 7415 |
rs778436999 | snp | C/T | | | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074610 | GCCTACACTCACATA[C/T]GGAAGCGGGGGCAGA | 7415 |
rs778524417 | snp | A/G | 1.65586e-05 | 0.00287733 | synonymous-codon | VCP | GRCh38.p7 | 9:35066702 | GTCGATACGCTTCCA[A/G]GAAGTACGGCTTAAG | 7415 |
rs778545123 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant | VCP | GRCh38.p7 | 9:35061553 | GACACTGTAACGCCT[A/G]GTCAGCCATCATCAT | 7415 |
rs778583473 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35060301 | TACATAGTTCAGCCT[A/G]TTGTAGCTCACCTTG | 7415 |
rs778635041 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | VCP | GRCh38.p7 | 9:35066841 | GACAAGCAGACTCCA[C/T]ATTACCAACCACACT | 7415 |
rs778643068 | snp | A/G | 1.75124e-05 | 0.00295903 | intron-variant | VCP | GRCh38.p7 | 9:35060262 | AGAAAAACAGCCTCT[A/G]TTCCTTGCCCTCAGG | 7415 |
rs778663878 | snp | A/C/G | 1.64741e-05 | 0.00286998 | intron-variant | VCP | GRCh38.p7 | 9:35062145 | GCCATGAGTCTGCCA[A/C/G]AACAGGATGTCTGGT | 7415 |
rs778771850 | in-del | -/A | | | intron-variant | VCP | GRCh38.p7 | 9:35068196 | GAAAAGAAACCTGGG[-/A]AAAATCCCTCAAGTA | 7415 |
rs778838414 | snp | G/T | 4.95217e-05 | 0.00497578 | intron-variant | VCP | GRCh38.p7 | 9:35063108 | GCAGAGTGTGATTAG[G/T]TTCCCACCTTCTCCC | 7415 |
rs778912220 | snp | A/T | 1.65405e-05 | 0.00287576 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074064 | CCTCCCCACAGAGAG[A/T]CAGCCCACTGGGGAC | 7415 |
rs778927516 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | VCP | GRCh38.p7 | 9:35059628 | GATGTCAGGCCGGTT[A/G]GTAGCGCCAATGATG | 7415 |
rs778931360 | in-del | -/A | | | intron-variant | VCP | GRCh38.p7 | 9:35060146 | AAGAGAGAGAGAGAG[-/A]AAAAAAAAATAACAC | 7415 |
rs779146901 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35070288 | AGAGGCCAAGCATGC[C/T]CAATGTGACAGTTGA | 7415 |
rs779183699 | in-del | -/C | 5.01073e-05 | 0.00500511 | intron-variant | VCP | GRCh38.p7 | 9:35067847 | TGTAATGCAGGCTAT[-/C]CTCTGGCCTCCCATC | 7415 |
rs779199730 | snp | C/T | 4.94776e-05 | 0.00497357 | intron-variant | VCP | GRCh38.p7 | 9:35057372 | ATGCTCCCAACCAAC[C/T]TACCTGAAGCTGCCA | 7415 |
rs779301958 | snp | C/T | 1.64936e-05 | 0.00287168 | missense | VCP | GRCh38.p7 | 9:35057164 | TGTATACACTGCCAC[C/T]TGTGCCGCCTCCACT | 7415 |
rs779387666 | snp | A/C | 1.648e-05 | 0.0028705 | intron-variant, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074326 | TCCAAGGACTCTAGG[A/C]CACCAACTGCCCCTC | 7415 |
rs779392075 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | VCP | GRCh38.p7 | 9:35060881 | GTGGCACCTCTACCA[C/T]GGTTTCCCGCAGTGC | 7415 |
rs779396698 | snp | C/T | 1.65608e-05 | 0.00287752 | intron-variant | VCP | GRCh38.p7 | 9:35065391 | TGTCTCCTGCGAGAG[C/T]AAACAGTACAAGCAC | 7415 |
rs779399540 | snp | C/T | 1.67175e-05 | 0.0028911 | intron-variant | VCP | GRCh38.p7 | 9:35059244 | GCAGCAGAGGTACCT[C/T]AGCATTTAGCCTCTC | 7415 |
rs779403243 | snp | C/T | 1.65515e-05 | 0.00287671 | synonymous-codon, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074454 | CCTCCGATCTAGCCT[C/T]TTCAGAGTCTGAAGC | 7415 |
rs779437638 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35068380 | AGAAGGAGGAAATGG[A/G]GTCAGTAGATACTCC | 7415 |
rs779458781 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35067247 | AGAAGAAAGCTACAT[A/G]AAACTTAGACTCCAT | 7415 |
rs779481226 | snp | A/T | 1.64738e-05 | 0.00286995 | intron-variant | VCP | GRCh38.p7 | 9:35060754 | GATCACCCAGATCAA[A/T]TACAATGTACTGAGA | 7415 |
rs779670266 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | VCP | GRCh38.p7 | 9:35059092 | TTTGTCTGCCTCTCT[C/T]GTTCTCGCCTAATCT | 7415 |
rs779785331 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35061877 | CTCTAGACAGGACGT[A/G]GGGTAAAGGAAAAAG | 7415 |
rs779819791 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35070818 | TCTGGCTCTGGAGAT[A/G]AGTGGTATGCCCTTT | 7415 |
rs779834525 | snp | A/G | 8.30903e-05 | 0.00644502 | stop-gained, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074489 | GAAAGTAAGTGTCTC[A/G]ATTACCTGTAGCCCC | 7415 |
rs779959657 | snp | C/T | 1.64876e-05 | 0.00287116 | missense | VCP | GRCh38.p7 | 9:35067915 | TCCCCTAGGCGTACA[C/T]GAAGGTTATTCCGAA | 7415 |
rs779975862 | snp | G/T | 1.64749e-05 | 0.00287005 | missense | VCP | GRCh38.p7 | 9:35060406 | GAAGTTGGCCTGGCA[G/T]TCATTAGCAATGGCT | 7415 |
rs780065574 | snp | C/T | 1.75164e-05 | 0.00295937 | intron-variant | VCP | GRCh38.p7 | 9:35060266 | AAACAGCCTCTATTC[C/T]TTGCCCTCAGGCAAA | 7415 |
rs780129670 | snp | A/C | 1.65274e-05 | 0.00287462 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074080 | CAGCCCACTGGGGAC[A/C]CAGCTCAAGCTCTTC | 7415 |
rs780139186 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon | VCP | GRCh38.p7 | 9:35064187 | AAAGAGGGCAGGATG[C/T]CTCAGGGGCAGTTCC | 7415 |
rs780306937 | snp | C/G/T | 1.67038e-05 | 0.00288992 | intron-variant | VCP | GRCh38.p7 | 9:35057554 | GGTAAACACAGATCA[C/G/T]TAGGGCTAGTTAAAG | 7415 |
rs780421436 | snp | C/T | 4.94548e-05 | 0.00497242 | intron-variant | VCP | GRCh38.p7 | 9:35068405 | TACTCCTGCCCCAAG[C/T]GCCTCGCCAGTCTCT | 7415 |
rs780426658 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon | VCP | GRCh38.p7 | 9:35060900 | TTCCCGCAGTGCTGA[C/T]GGGTTACTCTGGCTC | 7415 |
rs780521516 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant | VCP | GRCh38.p7 | 9:35061008 | GAGGCACGGGTGTGG[C/T]CCTTACCCGGAAGTC | 7415 |
rs780540495 | snp | A/G | 1.74127e-05 | 0.0029506 | intron-variant | VCP | GRCh38.p7 | 9:35066656 | GTCAATAATCCTTAA[A/G]CTCAGAATTAGCTCT | 7415 |
rs780808304 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35065782 | GAACAGAGAAGGGGA[A/G]AGATGGAGCAAAGGA | 7415 |
rs780860602 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35061975 | GGACCTAAGCAAGGA[C/T]GGGGTCAAAAGTATC | 7415 |
rs780865540 | snp | C/T | | | intron-variant | VCP | GRCh38.p7 | 9:35064481 | GCTTGAGTCCAGGAG[C/T]TCCTGGGCAATACAG | 7415 |
rs780896876 | snp | A/G | 6.58979e-05 | 0.00573974 | intron-variant | VCP | GRCh38.p7 | 9:35068113 | GGCTGACGGGGAGTA[A/G]GCAGCAGCCCTGGAG | 7415 |
rs780920397 | snp | A/C | | | upstream-variant-2KB | VCP | GRCh38.p7 | 9:35073031 | TCCTATTGTGGTAAC[A/C]CATACACCCATCTTC | 7415 |
rs780980572 | snp | C/G | 1.64749e-05 | 0.00287005 | intron-variant | VCP | GRCh38.p7 | 9:35061532 | AGTTCCCAGCAACTG[C/G]CTAGAGACACTGTAA | 7415 |
rs781092910 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant | VCP | GRCh38.p7 | 9:35062181 | GTGAAGTCAGGGCCT[C/T]TCAACCCCCCTCTAT | 7415 |
rs781182130 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | VCP | GRCh38.p7 | 9:35067964 | TCTTCTCATCAGAAC[A/C]AGTATCATCAGAAAG | 7415 |
rs781269203 | in-del | -/AG | 3.30006e-05 | 0.00406192 | intron-variant | VCP | GRCh38.p7 | 9:35061183 | TCATTGGCTACCTGC[-/AG]AGAGAAAGATCTACT | 7415 |
rs781273474 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon | VCP | GRCh38.p7 | 9:35064238 | TAGCTGCTTCCTGCA[A/G]CCACCAATGTCATCA | 7415 |
rs781299484 | snp | C/G | 5.24765e-05 | 0.00512206 | intron-variant | VCP | GRCh38.p7 | 9:35060570 | CTACCTCCACATTTT[C/G]AAAGAAACCTAACTA | 7415 |
rs781405879 | in-del | -/TGTTTTTT | | | intron-variant | VCP | GRCh38.p7 | 9:35071292 | TCCTTGGGCTGGCTG[-/TGTTTTTT]TTTTTTTTTTTTTTT | 7415 |
rs781479013 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant | VCP | GRCh38.p7 | 9:35065208 | CATGATGCCACACTG[A/G]GTAATCATAAAATCG | 7415 |
rs781498385 | snp | C/G | | | utr-variant-3-prime | VCP | GRCh38.p7 | 9:35056526 | GCCCAAGGCTGTTCC[C/G]AGGAAAAGAAGCAGG | 7415 |
rs781562072 | snp | A/G | 1.64876e-05 | 0.00287116 | synonymous-codon | VCP | GRCh38.p7 | 9:35057426 | CTGGGCAAACATCTC[A/G]TACTTCCGAATGTCA | 7415 |
rs781569592 | snp | C/G | 1.64749e-05 | 0.00287005 | intron-variant | VCP | GRCh38.p7 | 9:35064115 | AGGATTAGACATTGG[C/G]ACCACTTTAGACTTG | 7415 |
rs781606619 | snp | C/T | 1.66338e-05 | 0.00288386 | synonymous-codon | VCP | GRCh38.p7 | 9:35057525 | TGGATCATCCTCTTC[C/T]ACCTCCTATAGTTGG | 7415 |
rs781630725 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35068460 | AGTGAATAGATGAAG[C/G]TGTCCCTAGACCAGA | 7415 |
rs781725105 | snp | A/G | 1.65138e-05 | 0.00287343 | utr-variant-3-prime, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074089 | GGGGACCCAGCTCAA[A/G]CTCTTCAAAACGTGG | 7415 |
rs786204205 | snp | G/T | | | stop-gained, upstream-variant-2KB | FANCG, VCP | GRCh38.p7 | 9:35074384 | ACTAAGGGGTCACAT[G/T]AAGATGCTCTGTGGT | 7415 |
rs796102097 | in-del | -/AT | | | intron-variant | VCP | GRCh38.p7 | 9:35061710 | GGACAGTACACAAAC[-/AT]AAACAGGGCTCATCT | 7415 |
rs796141187 | in-del | -/A | | | intron-variant | VCP | GRCh38.p7 | 9:35058799 | CAAAAAACAAAAAAA[-/A]CCTTGCTGTGTTTGC | 7415 |
rs796234532 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35065555 | AGCAGCAGGCAAGAT[A/G]AGAAAGGTAAACTGT | 7415 |
rs796432390 | snp | A/C | | | intron-variant | VCP | GRCh38.p7 | 9:35058770 | AGACTTCGTCTCAAA[A/C]AAAAAACAAAAAACA | 7415 |
rs796461880 | snp | C/G | | | intron-variant | VCP | GRCh38.p7 | 9:35069132 | CCAAAGGAATGCCAA[C/G]CATAAAGACCATCAT | 7415 |
rs796854805 | snp | A/G | | | intron-variant | VCP | GRCh38.p7 | 9:35071591 | CCTAAAATGTTAAAG[A/G]AAAATTCCTTTCTCC | 7415 |
rs863225291 | snp | A/T | | | missense | VCP | GRCh38.p7 | 9:35067922 | AGAGTTGTTCGGAAT[A/T]ACCTTCGTGTACGCC | 7415 |
rs864309501 | snp | A/G | | | missense | VCP | GRCh38.p7 | 9:35065274 | ACAGTGATCCACTGC[A/G]AAGGGGAGCCTATCA | 7415 |
rs864309502 | snp | A/G | | | missense | VCP | GRCh38.p7 | 9:35067903 | TTCGTGTACGCCTAG[A/G]GGATGTCATCAGGTG | 7415 |