SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12516 | snp | C/T | 0.493918 | 0.0548094 | BRCA1 | 17 | allele_origin=T(unknown)/C(germline) | 17:43044391 | CTTCCCTAGCCCCCC[C/T]AGTGTGCAAGGGCAG | 672 |
rs16940 | snp | C/T | 0.450049 | 0.149935 | BRCA1 | 17 | allele_origin=T(germline)/C(germline,somatic) | 17:43093220 | AGTAGCAGTATTTCA[C/T]TGGTACCTGGTACTG | 672 |
rs16941 | snp | A/G | 0.450618 | 0.149173 | BRCA1 | 17 | allele_origin=G(inherited)/A(germline)/C(inherited) | 17:43092418 | AAAATGTTTTTAAAG[A/G]AGCCAGCTCAAGCAA | 672 |
rs16942 | snp | A/G | 0.454401 | 0.143945 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091983 | GCAAAAGCGTCCAGA[A/G]AGGAGAGCTTAGCAG | 672 |
rs709630 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100655 | atataacatatatat[A/T]acatatatatatata | 672 |
rs799901 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121305 | gcctgaacccgggag[G/T]cggagctggcagtga | 672 |
rs799902 | snp | C/T | 0.496034 | 0.0443518 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121331 | agtgagccaagatcg[C/T]gccactgcactccag | 672 |
rs799903 | snp | A/G | 0.496348 | 0.0425753 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122889 | gcctctactaaaaaa[A/G]aaaaaaaaatacaaa | 672 |
rs799905 | snp | C/G | 0.499242 | 0.0194585 | BRCA1, NBR2 | 17 | allele_origin=G(germline)/C(unknown) | 17:43125170 | CCGCCCCTACCCCCC[C/G]TCAAAGAATACCCAT | 672 |
rs799906 | snp | C/T | 0.49998 | 0.00319482 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126099 | CTGGGGCAAGTAGTC[C/T]TGTAAGGTCAGTGGC | 672 |
rs799907 | snp | C/G | 0.253824 | 0.249971 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126708 | ctcgctcgctctcgg[C/G]gcctcctcggccttg | 672 |
rs799908 | snp | A/G | 0.49998 | 0.00319482 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126899 | gccagcgcgagttcc[A/G]ggtgggcgcgggctc | 672 |
rs799909 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127210 | gagaggagtgcaggc[A/G]cccggcacagccctg | 672 |
rs799911 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104565 | accaacaatgtaagt[G/T]gcactattatttcgt | 672 |
rs799912 | snp | C/T | 0.495291 | 0.0482933 | BRCA1 | 17 | allele_origin=T(germline)/C(unknown) | 17:43105117 | GTATAAACCGTGTGA[C/T]GGCAGTGATTTAGTA | 672 |
rs799913 | snp | C/T | 0.221439 | 0.248363 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106929 | ctcaccacaaagcta[C/T]agtaatcaagaaagt | 672 |
rs799914 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107764 | aatgaaattatactc[C/T]tatctcacaccaaat | 672 |
rs799916 | snp | A/C | 0.499989 | 0.00239614 | BRCA1 | 17 | allele_origin=A(germline)/C(somatic) | 17:43091173 | TATAAAAGCAAATCC[A/C]GGTGTCCCAAAGCAA | 672 |
rs799917 | snp | C/T | 0.483818 | 0.0884827 | BRCA1 | 17 | allele_origin=G(inherited)/T(inherited)/A(inherited)/C(germline) | 17:43092919 | GCCAGTCATTTGCTC[C/T]GTTTTCAAATCCAGG | 672 |
rs799918 | snp | C/G | 0.154329 | 0.23097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098010 | TTGAGAGCCCAGTTT[C/G]AATTCTGAGCTCAGC | 672 |
rs799919 | snp | C/T | 0.495368 | 0.0478996 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098906 | cactgcaacctctgc[C/T]tcctgggttcaagcg | 672 |
rs799921 | snp | C/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099080 | cgcccacctcggcct[C/T]ccaaagtgctgggat | 672 |
rs799922 | snp | C/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099203 | ATCCATCATGTTTTT[C/T]CTTATTGCTACTCTC | 672 |
rs799923 | snp | A/G | 0.287174 | 0.247221 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43099914 | AACAGTCAAGCAATT[A/G]TTGGCCAGTTCTGTG | 672 |
rs799924 | snp | A/G | 0.10237 | 0.201756 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100560 | tgtgtgtgtgtgtgt[A/G]tatatatatataaca | 672 |
rs799925 | snp | A/G | 0.204496 | 0.245824 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100594 | atataacatatatat[A/G]ttatatatatataac | 672 |
rs799926 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100633 | aacatatatatatgt[A/T]atatatatataacat | 672 |
rs808955 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100510 | ctatgcctggctaat[A/T]tgtgtGTGTGTGTGt | 672 |
rs966018 | snp | G/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056633 | caggccagagtgcag[G/T]ggtgcgatctcagct | 672 |
rs1060915 | snp | C/T | 0.450766 | 0.148973 | BRCA1 | 17 | allele_origin=T(germline)/C(germline,somatic) | 17:43082453 | CATCATAAGTGACTC[C/T]TCTGCCCTTGAGGAC | 672 |
rs1060920 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044784 | ATGAAACTAGAAGAG[A/G]TTTCTAAAAGTCTGA | 672 |
rs1060921 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044778 | CTAGAAGAGATTTCT[A/T]AAAGTCTGAGATATA | 672 |
rs1709432 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112934 | tgcctgtaatcccag[C/T]tacttgggaggctga | 672 |
rs1709437 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114423 | agtctccctcttgtc[G/T]cccaggctggaatgc | 672 |
rs1709438 | snp | A/G | 0.0198 | 0.0975087 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114435 | gtcgcccaggctgga[A/G]tgcagtggcatgatc | 672 |
rs1709440 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104579 | ttgcactattatttt[C/G]tgtatcactaagaaa | 672 |
rs1709441 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116661 | cgtggtggcgcacgc[C/G]tgtagttccaactac | 672 |
rs1793979 | snp | A/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116695 | ccaactctactaaaa[A/T]tacgaaaaatcagcc | 672 |
rs1793980 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114462 | TCCATAATTTTCATC[C/T]Gagtgagctaagatc | 672 |
rs1793981 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114290 | TGAACTGTATGTTTT[A/C]TGGTCAGCTTGAGTA | 672 |
rs1793982 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114288 | AACTGTATGTTTTAT[G/T]GTCAGCTTGAGTAAC | 672 |
rs1793984 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112844 | tgcactccagcctgg[C/G]cgacaagagtgaaaa | 672 |
rs1793986 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104841 | ATATCCCAAGAATGA[A/C]ACTCAAGTGCTGTCC | 672 |
rs1793989 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123452 | tgaggcaggagaatc[A/C]cttgaaccaggaggc | 672 |
rs1799736 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097295 | TTTTGGGGGGAAATT[-/T]TTTAGGATCTGATTC | 672 |
rs1799949 | snp | C/T | 0.453953 | 0.144579 | BRCA1 | 17 | allele_origin=T(germline,somatic)/C(germline) | 17:43093449 | TAAAAGACATGACAG[C/T]GATACTTTCCCAGAG | 672 |
rs1799950 | snp | A/G | 0.0842568 | 0.187161 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094464 | AAGAATGGAATAAGC[A/G]GAAACTGCCATGCTC | 672 |
rs1799965 | snp | C/T | 0.00293366 | 0.0381867 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43097246 | TAAGGCAACTTATTG[C/T]AGGTGAGTCAAAGAG | 672 |
rs1799966 | snp | A/G | 0.454828 | 0.143493 | BRCA1 | 17 | allele_origin=G(inherited)/T(inherited)/A(germline) | 17:43071077 | GCAGAATCTGCCCAG[A/G]GTCCAGCTGCTGCTC | 672 |
rs1799967 | snp | A/G | 0.0346163 | 0.126925 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43070958 | CAAAAGAATGTCCAT[A/G]GTGGTGTCTGGCCTG | 672 |
rs1800062 | snp | A/G/T | 0.00824027 | 0.0636571 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43115746 | ACCTGTCTCCACAAA[A/G/T]TGTGACCACATATTT | 672 |
rs1800063 | snp | A/G | 0.0016954 | 0.0290659 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094550 | TGGAAGTAAGGAAAC[A/G]TGTAATGATAGGCGG | 672 |
rs1800064 | snp | A/G/T | 4.94907e-05 | 0.00497422 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43093665 | CAGGCATATTCATGC[A/G/T]CTTGAACTAGTAGTC | 672 |
rs1800704 | snp | A/G | 0.00171478 | 0.029231 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092507 | TGAGGAACATTCAAT[A/G]TCACCTGAAAGAGAA | 672 |
rs1800707 | snp | G/T | 0.0122029 | 0.0771528 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082543 | ACATAACCTGATAAA[G/T]CTCCAGCAGGAAATG | 672 |
rs1800709 | snp | C/T | 0.00343882 | 0.0413229 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093010 | GAAGTTAACCACAGT[C/T]GGGAAACAAGCATAG | 672 |
rs1800726 | snp | A/C/G | 0 | 0 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43070993 | AAGCCAGAATTGACA[A/C/G]CTTCAACAGAAAGGG | 672 |
rs1800740 | snp | A/G | 0.0016959 | 0.0290702 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092798 | GGAAGAAAATCAAGG[A/G]AAGAATGAGTCTAAT | 672 |
rs1800744 | snp | G/T | 0.00429257 | 0.0461287 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43074471 | GGTGGTACATGCACA[G/T]TTGCTCTGGGAGTCT | 672 |
rs1800747 | snp | A/C/G/T | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43063952 | GTTTTTCATTCTGCA[A/C/G/T]ATGCTGAGTTTGTGT | 672 |
rs1800751 | snp | C/G/T | 0 | 0 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43047676 | ATTGTGGTTGTGCAG[C/G/T]CAGATGCCTGGACAG | 672 |
rs1800757 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051069 | CCCTTCACCAACATG[C/T]CCACAGGTAAGAGCC | 672 |
rs2070833 | snp | A/C | 0.140581 | 0.224783 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090832 | TTTGAATTAATGGCA[A/C]AATTGTTTGTGGTTC | 672 |
rs2070834 | snp | A/C | 0.456568 | 0.140818 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090268 | ACTCTGCATAGCTCC[A/C]TTTTAAGAATATGCC | 672 |
rs2187603 | snp | A/G | 0.438246 | 0.16451 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061876 | TTTTATAGGCCAGGC[A/G]TGGTGGCTCATGCCT | 672 |
rs2227945 | snp | A/G | 0.00620014 | 0.055332 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092113 | CAGCCTATGGGAAGT[A/G]GTCATGCATCTCAGG | 672 |
rs2236762 | snp | A/T | 0.499989 | 0.00239614 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074658 | GACTTCTAGGCTGTC[A/T]TGCGGGCTCTTTTTT | 672 |
rs2236763 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074016 | TAATCCCAGTACTCC[A/C]GGAGGCCGAGGCAGG | 672 |
rs2355967 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072897 | CCCCACCCCCCtttt[C/T]atagagatcaggtct | 672 |
rs2671874 | snp | A/G | 0.251014 | 0.249998 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113938 | aaattagctgggtgt[A/G]gtggcagatgcctgt | 672 |
rs2854689 | snp | A/G | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114175 | gaggccaaggcagga[A/G]gatcacttaaggcca | 672 |
rs3092986 | snp | A/G | 0.0425829 | 0.139564 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125979 | ACAACACTCCAGTCC[A/G]TAACTGTTGACAAGT | 672 |
rs3092987 | snp | A/G | 0.447162 | 0.153712 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070706 | GAGAAAATAATTATT[A/G]AATATTAGTGGAAAA | 672 |
rs3092988 | snp | A/G | 0.438806 | 0.163867 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049685 | CTGAGTCTCTAACCA[A/G]GATAACATGTATTTT | 672 |
rs3092994 | snp | A/G | 0.450357 | 0.149522 | BRCA1 | 17 | allele_origin=G(germline)/A(germline,somatic) | 17:43063808 | ATTTTTACACCTAAC[A/G]TTTAACACCTAAGGT | 672 |
rs3092995 | snp | C/G/T | 0.00970359 | 0.0689765 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43045642 | AGAGCCACAGGACCC[C/G/T]AAGAATGAGCTTACA | 672 |
rs3220757 | microsatellite | (CA)17/19/20/21/22/23/24/25 | 0.826062 | 0.0733934 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052782 | ACAGACGGACAGAAA[(CA)17/19/20/21/22/23/24/25]TCTTACTTTACCACC | 672 |
rs3737559 | snp | A/G | 0.120326 | 0.21374 | BRCA1 | 17 | allele_origin=G(germline)/A(unknown) | 17:43082287 | CTTGCTCAGCACATG[A/G]GTAATTATGGAGCCT | 672 |
rs3765640 | snp | C/T | 0.457154 | 0.139954 | BRCA1, NBR2 | 17 | allele_origin=T(germline)/C(germline) | 17:43124230 | TTCTTTGGTTTGTAT[C/T]ATTCTAAAACCTTCC | 672 |
rs3785546 | snp | C/T | 0.44858 | 0.151875 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064916 | GCTCACGGCAAGCTC[C/T]GCCTCCTGGGTTCAT | 672 |
rs3950989 | snp | A/G | 0.456568 | 0.140818 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085936 | AATAAGCCTAATCCA[A/G]ATACAAGCTGAAGTC | 672 |
rs4239147 | snp | C/T | 0.499987 | 0.00259581 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077795 | ggtgagccaagatca[C/T]gccattgcactgcag | 672 |
rs4239148 | snp | C/T | 0.495213 | 0.048687 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077840 | gctgaggcaggagaa[C/T]agcttgaacctggga | 672 |
rs4318274 | snp | A/T | 0.495368 | 0.0478996 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077891 | aaaattagttgggcg[A/T]ggtggtgcatacctg | 672 |
rs4438367 | snp | A/G | | | synonymous-codon, missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047677 | AATTGTGGTTGTGCA[A/G]CCAGATGCCTGGACA | 672 |
rs4792972 | snp | C/T | 0.345679 | 0.230967 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048520 | tttctctctctctct[C/T]tttttttttttttag | 672 |
rs4792977 | snp | A/G | 0.456803 | 0.140473 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108791 | agaggtcaggagttc[A/G]agaccagcctgacca | 672 |
rs4793190 | snp | C/T | 0.450483 | 0.149354 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048092 | gtagacatgaggtcc[C/T]actgtattgcccagg | 672 |
rs4793191 | snp | A/G | 0.450609 | 0.149185 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052360 | ATCATAGCTTGCTGC[A/G]GTATTGAACTTCTGG | 672 |
rs4793192 | snp | C/T | 0.450483 | 0.149354 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052373 | GCAGTATTGAACTTC[C/T]GGGCTCAAGCAATCC | 672 |
rs4793193 | snp | A/C | 0.450483 | 0.149354 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060321 | TGCTGGGATTACAGG[A/C]ATGAGCCACCACACC | 672 |
rs4793194 | snp | A/G | 0.457154 | 0.139954 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066316 | TGTTAAGACTATCTC[A/G]GAGCTGTTATCAGAC | 672 |
rs4793195 | snp | C/T | 0.446118 | 0.155041 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066555 | agctgggattacagg[C/T]gcacaccaccacgcc | 672 |
rs4793197 | snp | A/G | 0.44546 | 0.155869 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079885 | TCTTCTTACTACAAT[A/G]GGCCTCATGCAATGA | 672 |
rs4793203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117310 | AGCCGGGCGTGGTGG[C/T]GCATGCCTGTGGTCT | 672 |
rs4793204 | snp | A/G | 0.457504 | 0.139435 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127281 | agatggggacttgga[A/G]aacttttatgtctag | 672 |
rs4986844 | snp | A/G | 0.0010381 | 0.0227591 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093422 | AGAGCTGAAGTTAAC[A/G]AATGCACCTGGTTCT | 672 |
rs4986845 | snp | A/G | 0.00113753 | 0.0238217 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093364 | CTTAAAGAATTTGTC[A/G]ATCCTAGCCTTCCAA | 672 |
rs4986846 | snp | C/G/T | 0.000313074 | 0.0125078 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43093299 | AGTGTCTAATAATGC[C/G/T]GAAGACCCCAAAGAT | 672 |
rs4986847 | snp | A/C/G | 0.000214184 | 0.0103463 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43092758 | GTACAGACAGTTAAT[A/C/G]TCACTGCAGGCTTTC | 672 |
rs4986848 | snp | C/T | 0.00724606 | 0.0597539 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092565 | TTCCCATCAAGTCAT[C/T]TGTTAAAACTAAATG | 672 |
rs4986849 | snp | A/G | 1.6477e-05 | 0.00287024 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43082433 | CCCTTGAGGACCTGC[A/G]AAATCCAGAACAAAG | 672 |
rs4986850 | snp | A/G | 0.107174 | 0.205184 | BRCA1 | 17 | allele_origin=G(germline)/T(inherited)/A(inherited) | 17:43093454 | ACAAGTAAAAGACAT[A/G]ACAGCGATACTTTCC | 672 |
rs4986852 | snp | A/G | 0.0259868 | 0.110987 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092412 | TTTTTAAAGAAGCCA[A/G]CTCAAGCAATATTAA | 672 |
rs4986854 | snp | C/T | 0.00304288 | 0.0388868 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43071031 | CTGGGTATAATGCAA[C/T]GGAAGAAAGTGTGAG | 672 |
rs5031012 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070915 | TTTGTGAGTGTATCC[A/G]TATGTATCTCCCTAA | 672 |
rs5820482 | in-del | -/A | 0.113334 | 0.209338 | BRCA1 | 17 | allele_origin=A(germline)/(germline) | 17:43073638 | TATTCATTAACTCAT[-/A]AAAAAAACTTGCTTT | 672 |
rs5820483 | in-del | -/CCT | 0.45237 | 0.146787 | BRCA1 | 17 | allele_origin=T(germline,somatic)/(germline) | 17:43095105 | TATGCAGAAACCACA[-/CCT]CCTATTTCTCTAACG | 672 |
rs6416927 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080327 | GTAGctcccaagtag[C/G]tgggattacaggcat | 672 |
rs6503725 | snp | A/G | 0.251296 | 0.249997 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053704 | TTTCAGGCcgggcgc[A/G]gtggcctgtaatcct | 672 |
rs7212284 | snp | A/G | 0.499809 | 0.00978247 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053924 | CGGTGAGCCAAGATC[A/G]CGCCATTGTACTTCA | 672 |
rs7219966 | snp | A/G | 0.10237 | 0.201756 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099491 | ggctaggctggtctc[A/G]aactcccgacctcag | 672 |
rs7406624 | snp | A/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077745 | tttttatttatttat[A/T]ttttttgagatggag | 672 |
rs7502059 | snp | A/G | 0 | 0 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093150 | TTTGGTTCTGTTTTT[A/G]CCTTCCCTAGAGTGC | 672 |
rs7503154 | snp | A/C | 0.456657 | 0.140687 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095587 | ACCCCATCTCAAAAA[A/C]AAACAAACAAACAAA | 672 |
rs8065872 | snp | A/T | 0.0799831 | 0.183287 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109546 | CAAGTACCATATTGC[A/T]CTCAACAAAACAATG | 672 |
rs8066171 | snp | A/C | 0.0810805 | 0.184299 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058314 | aggagttggaggctg[A/C]agtgaactgtgatca | 672 |
rs8067269 | snp | A/G | 0.485392 | 0.0842056 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083782 | CCATTTCAAAGAAGA[A/G]TGTGCTAAGTCCAAG | 672 |
rs8068463 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047161 | CTGGAGTACAGTGGT[A/G]TGATCGTGGCTCACT | 672 |
rs8070179 | snp | A/G | 0.497151 | 0.037632 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050671 | GCTCTGGGCCCGTCC[A/G]TGGTGGGCCAGCTGC | 672 |
rs8074462 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116581 | tggcatgcaatggtg[C/T]gatctcggctcactg | 672 |
rs8077486 | snp | C/T | 0.499784 | 0.0103811 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060788 | ctgggattataggca[C/T]gagccaccacacacg | 672 |
rs8080934 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057863 | caaacaaacaaaaaa[A/C]ccaaaaattagctgg | 672 |
rs8176071 | in-del | -/ACA | 0.456568 | 0.140818 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125988 | TACGAAAACATAACA[-/ACA]CTCCAGTCCATAACT | 672 |
rs8176072 | snp | A/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125927 | ATCTATCCACTGGAT[A/T]TCCGTGAGAATTGTG | 672 |
rs8176073 | snp | A/G | 0.0115603 | 0.0751433 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125816 | CGCATGCTGGAAATA[A/G]TTATTTCCCTCCACC | 672 |
rs8176074 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125748 | GGAGACCTCCATTAG[A/G]GCGGAAAGAGTGGGG | 672 |
rs8176075 | in-del | -/T | 0.0112991 | 0.0743093 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125397 | CGCGGGAATTACAGA[-/T]AAATTAAAACTGCGA | 672 |
rs8176076 | snp | C/T | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124935 | aacgtggtgaaactc[C/T]gtctctactaaaaat | 672 |
rs8176077 | snp | A/G | 0.457154 | 0.139954 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124331 | CAAGGGGTTGGCAGC[A/G]ATATGTGAAAAAATT | 672 |
rs8176078 | in-del | -/TGT | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124171 | ATGATAAAATGAAGT[-/TGT]CATTTTATAAACCTT | 672 |
rs8176079 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123815 | TCTGCCTCTCCCACT[C/T]CTCTCCTTTTCAACA | 672 |
rs8176080 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123785 | ACAAATCCTGTGGTC[C/T]GGGAAAGACAGGGAC | 672 |
rs8176081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123784 | CAAATCCTGTGGTCC[A/G]GGAAAGACAGGGACT | 672 |
rs8176082 | snp | C/T | 0.457154 | 0.139954 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123628 | GAGGGCGGTGGCTTA[C/T]GCCTGTAATCCCAGC | 672 |
rs8176083 | snp | C/G | 0.445592 | 0.155704 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123134 | AAGCAATCCTCCCAC[C/G]TCAGCCTCCAGAGTA | 672 |
rs8176085 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122772 | ggcataagccactgc[A/G]tccagccattcttgt | 672 |
rs8176086 | snp | C/T | 0.457154 | 0.139954 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122761 | ctgcgtccagccatt[C/T]ttgtatttttctgtt | 672 |
rs8176087 | snp | G/T | 0.445592 | 0.155704 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118649 | aggcattcaagacca[G/T]catgggcatcatagt | 672 |
rs8176088 | snp | C/T | 0.456568 | 0.140818 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118446 | gaggttacagagagc[C/T]gagatggtgccactg | 672 |
rs8176089 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118425 | GGTGCCACTGCACTC[C/T]AGCCTGGGCGACAGA | 672 |
rs8176090 | snp | C/G | 0.089084 | 0.191327 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118401 | cgacagaacgagact[C/G]tgtctgaaaaaaaaa | 672 |
rs8176091 | snp | A/G | 0.445855 | 0.155373 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118260 | gattattacatttta[A/G]caccttgacctatct | 672 |
rs8176092 | snp | A/C | 0.456803 | 0.140473 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118212 | ggcatggtcctgctc[A/C]gggtttgccttctct | 672 |
rs8176093 | snp | A/C | 0.00335007 | 0.0407899 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117918 | tttgtaaactgctac[A/C]tttctatctcctaga | 672 |
rs8176094 | snp | A/T | 0.0121208 | 0.0768991 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117293 | caccacgcccggcta[A/T]tttttgtatttttag | 672 |
rs8176095 | snp | C/T | 0.030665 | 0.119967 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116729 | gagttcaagaccagc[C/T]ggccaacatggtgaa | 672 |
rs8176096 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116501 | GGTTTGGGTGTGTTG[A/G]CTCATGCCTGTAAAC | 672 |
rs8176097 | in-del | -/A/AA | 0.462045 | 0.150414 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116191 | GCATTTACAGTAAAC[-/A/AA]AAAAAAAAGTTCTAG | 672 |
rs8176098 | snp | G/T | 0.456803 | 0.140473 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116189 | TAAACAAAAAAAAGT[G/T]CTAGGAAGGAATTCA | 672 |
rs8176100 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115615 | TCAATTAAGTGAGAA[C/T]GAAAAATCCAACTCC | 672 |
rs8176101 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115524 | GTAAAGTTTTGACAT[A/T]TATTATCtttttttt | 672 |
rs8176102 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115163 | TTTTGTATTTTTTGT[A/G]TCCATCAGTGAAAGC | 672 |
rs8176103 | snp | C/T | 0.457504 | 0.139435 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115033 | GGGTCAGTGTTTGCC[C/T]GCTTTGTAATCATTG | 672 |
rs8176104 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114980 | ACCAGTTTCTATTTA[A/G]GCCAAAATTCATTTA | 672 |
rs8176105 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114939 | TCAAGTTATATTTAC[A/G]TATTTGATGATCTTG | 672 |
rs8176106 | snp | A/C | 0.021333 | 0.101051 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114094 | gatgacagagtgaga[A/C]cctgtcttttttttt | 672 |
rs8176107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114048 | tcactctattgccca[A/G]gctggagtgcagtgg | 672 |
rs8176108 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113790 | tggctGACCCTGTCT[C/G]TTAACAAAAAAAGAG | 672 |
rs8176109 | snp | C/T | 0.456803 | 0.140473 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113759 | AGATTAAGTTATGAA[C/T]ATAGTTGCTTTGAGA | 672 |
rs8176110 | snp | A/G | 0.0121208 | 0.0768991 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112880 | ggaggcggaggttgc[A/G]gtgagccgagattgc | 672 |
rs8176112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112699 | ATAGTCAGGAAAGAA[C/T]CAGTCataaagatat | 672 |
rs8176113 | snp | G/T | 0.0131862 | 0.0801202 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112459 | tgcccagctaatttt[G/T]aagtttcttgtagag | 672 |
rs8176114 | snp | C/T | 0.445196 | 0.1562 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112347 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGTG | 672 |
rs8176115 | snp | A/T | 0.0114282 | 0.0747228 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112073 | TATAATGCCCATGTG[A/T]TAGATCGACTTTTTC | 672 |
rs8176116 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111828 | ttgtttttgtttgtt[G/T]tgttttgagacggag | 672 |
rs8176117 | snp | A/G | 0.459118 | 0.137002 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111549 | caagtgtgagccacc[A/G]cgcccggctGttttt | 672 |
rs8176118 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111413 | cctgcctcagcctcc[C/T]gagtagctgggacta | 672 |
rs8176119 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110085 | aacatggtgaaaccc[C/T]gcctctactaaaatt | 672 |
rs8176120 | snp | A/G | 0.457037 | 0.140127 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109216 | TGAGGTCAGGAGTTC[A/G]AGACCAGACTGGGCA | 672 |
rs8176121 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109088 | gcgatcacttgaggt[C/G]gggagttcaagactg | 672 |
rs8176124 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107539 | caaaaaattagctgg[A/G]tatggtggtgcatgt | 672 |
rs8176125 | snp | G/T | 0.0176977 | 0.0923885 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107474 | agaattgcttgagcc[G/T]aggaggtggaggttg | 672 |
rs8176126 | snp | A/G | 0.456803 | 0.140473 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107032 | TTATTGTTGAAAATC[A/G]CTTGATCACAGATGT | 672 |
rs8176127 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106809 | ATCATTAAATATGCC[A/G]TATTAACTTTTATTA | 672 |
rs8176128 | snp | A/T | 0.00696011 | 0.05858 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43106433 | ATTTGGTAATGATGC[A/T]AGGTTGGAAGCAACC | 672 |
rs8176129 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106194 | AAAGTAGGGCTGTAT[A/C/T]GCCGTGCCCCCATTG | 672 |
rs8176130 | snp | A/G | 0.456803 | 0.140473 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106026 | CCTCTTCCTGCCTTA[A/G]CCTCCCAAATAGCTG | 672 |
rs8176131 | snp | A/G | 0.0134222 | 0.0808143 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105942 | atgaggttttaccat[A/G]ttgcccaggctggta | 672 |
rs8176132 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105799 | TGTATCTCTTCTGCT[A/G]CAATGTAAATTCTAT | 672 |
rs8176133 | snp | G/T | 0.446118 | 0.155041 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105441 | TCAGCCTGGGCAACA[G/T]AGTGAGACCCCATCA | 672 |
rs8176134 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105222 | GTACTCTAGTTTTCT[A/G]TGCAATGCATTATAT | 672 |
rs8176135 | snp | C/T | 0.00457308 | 0.0475986 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104302 | TAATTCATACATTTT[C/T]CTCTAACTGCAAACA | 672 |
rs8176136 | snp | G/T | 0.0111728 | 0.0739025 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103904 | ggccaggctggtctc[G/T]aactcctaacctcag | 672 |
rs8176137 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103842 | tgggattacaggtgt[A/G]agccactgtgcccgg | 672 |
rs8176138 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100215 | ACAACAGAAAAAAAA[-/A]TTCAAATCACACATA | 672 |
rs8176139 | snp | G/T | 0.00333889 | 0.0407222 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099883 | CTTTACCATACTGTT[G/T]AGCAGGAAACCAGTC | 672 |
rs8176140 | snp | A/T | 0.456568 | 0.140818 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43099629 | ATGGTGAGTTATAAA[A/T]AATGTAAAAGACGCA | 672 |
rs8176141 | snp | C/G | 0.446118 | 0.155041 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099478 | TTCGAGACCAGCCTA[C/G]CCAACATGGAGAAAC | 672 |
rs8176142 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098749 | agaccgaggcagaag[A/G]attggttgagtccac | 672 |
rs8176143 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097369 | ctagttgaatATCTG[C/T]TTTTCAACAAGTACA | 672 |
rs8176144 | in-del | -/T | 0.44546 | 0.155869 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43097347 | ACAAGTACATTTTTT[-/T]AACCCTTTTAATTAA | 672 |
rs8176145 | snp | C/T | 0.456568 | 0.140818 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097077 | TTGGGATTTGGTGTA[C/T]AGATTTTTTTCATCA | 672 |
rs8176146 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096887 | tagtggaggaaaTAC[C/T]CTTTTTGTTTGTTGG | 672 |
rs8176147 | snp | A/G | 0.445592 | 0.155704 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096147 | TCAAGTGGTCCACCC[A/G]CCTCAGCCTCCCAAA | 672 |
rs8176148 | snp | C/T | 0.0121208 | 0.0768991 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096078 | CCATTTCATTTCAAC[C/T]AGAAGTTTCTAAAGG | 672 |
rs8176149 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095705 | GAGTATCATTCTCTG[A/T]CAAATGTCGTGGTAT | 672 |
rs8176151 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095038 | GTGGAAATAATCTAG[A/G]TAAATAGGAATTAAA | 672 |
rs8176152 | in-del | -/T | 0.0114282 | 0.0747228 | intron-variant | BRCA1 | GRCh38.p7 | 17:43094872 | TACCTTGTTATTTTT[-/T]GTATATTTTCAGCTG | 672 |
rs8176153 | snp | A/G | 0.00133739 | 0.0258246 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094708 | CATGTGGAGCCATGT[A/G]GCACAAATACTCATG | 672 |
rs8176154 | snp | A/G | 6.59663e-05 | 0.00574272 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093653 | TGCGCTTGAACTAGT[A/G]GTCAGTAGAAATCTA | 672 |
rs8176155 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090381 | atctcaaaaacaaac[A/G]aacaaaaaCACATCA | 672 |
rs8176157 | snp | C/T | 0.0121208 | 0.0768991 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089642 | gagaatcacttgaac[C/T]caggaggcggaggtt | 672 |
rs8176158 | snp | A/G | 0.427438 | 0.176113 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089552 | CTCAAAAAAAAAAAA[A/G]AAGAAAGTACACAAT | 672 |
rs8176159 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089503 | TGGTCAAGGCCAATA[A/C]TTTGGTCACCTATGA | 672 |
rs8176160 | snp | A/G | 0.457037 | 0.140127 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089486 | TTGGTCACCTATGAA[A/G]TAAATAAAAGCTTTA | 672 |
rs8176161 | snp | G/T | 0.457037 | 0.140127 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089373 | ACAACGTCTAAAAAT[G/T]AATATCATCTTCATC | 672 |
rs8176162 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089157 | gctcatttttttgta[G/T]ttttttagtagagag | 672 |
rs8176163 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088898 | AATAATTAGGTTGGT[C/T]CTTTGTATTCCCAGC | 672 |
rs8176164 | snp | C/T | 0.0116955 | 0.0755709 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088793 | TGATCTTAGACAGTT[C/T]GCTTATGTTCTCTGA | 672 |
rs8176165 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088733 | CTGTTCAGACCCCCT[C/T]GATTCATCCTGCTGT | 672 |
rs8176166 | snp | A/G | 0.282632 | 0.247861 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088260 | TTTGGGATGATGAAA[A/G]AGTTCTGGAGATAGA | 672 |
rs8176167 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087963 | ggaggtcaaggctgc[A/G]gtgagttgtgatcac | 672 |
rs8176168 | snp | C/T | 0.457154 | 0.139954 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087611 | gcagtggtgtgacct[C/T]ggctcaccgcatcct | 672 |
rs8176169 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087610 | cagtggtgtgacctt[A/G]gctcaccgcatcctc | 672 |
rs8176170 | snp | A/G | 0.457154 | 0.139954 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087474 | ggtttctccatgttg[A/G]ccaggctggtctcaa | 672 |
rs8176171 | snp | C/T | 0.44755 | 0.153212 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087455 | ggctggtctcaaact[C/T]ctggcctcaagtgat | 672 |
rs8176172 | snp | A/C | 0.0108105 | 0.0727212 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087054 | ttttcctgtaccttg[A/C]caacactgggtgata | 672 |
rs8176173 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086602 | CTTATTCCCAGAGAT[A/G]TGTCTATTTGTTCAG | 672 |
rs8176174 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085995 | TTGAAAATATTCACA[A/T]CATGTCGACAAAACT | 672 |
rs8176175 | in-del | -/T | 0.0333695 | 0.124785 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085676 | CCTCCTGGTGGGGAC[-/T]TTAAGGAGACATTCA | 672 |
rs8176176 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085427 | TGACTAACAATTATA[C/T]AGTGTTCAAAAAGTA | 672 |
rs8176177 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085058 | AAGTCTTAGAAACCT[A/G]TTGGTTTTATTCTCC | 672 |
rs8176178 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084625 | CAGTGTAGCAGGAGA[A/G]AGAAGATGGCTTGTT | 672 |
rs8176179 | snp | C/T | 0.0116955 | 0.0755709 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084394 | cagatcacctgaggt[C/T]aggagttcaagacca | 672 |
rs8176180 | snp | A/T | 0.0116955 | 0.0755709 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084286 | tcccagcactttggg[A/T]ggccgaggcgggagg | 672 |
rs8176181 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084026 | aaaaaaaaaattagt[C/T]gggcatggtaacagg | 672 |
rs8176182 | snp | A/G/T | 0.0197799 | 0.097547 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083822 | GAAAACTCCTTACAT[A/G/T]CCTAAATTCTTTGTT | 672 |
rs8176183 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082676 | TCCATACTAGGTGAT[G/T]TCAATTCCTGTGCTA | 672 |
rs8176185 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082024 | TAACACTGGTGTCAC[A/G]TCACAAAGACCTATT | 672 |
rs8176186 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081610 | GGAGATGCTAGGCAT[A/G]GGGTCCCCACTAGGA | 672 |
rs8176187 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081192 | TTCTTTAGGGTACTT[C/T]CACCATCTTCAGTCT | 672 |
rs8176188 | snp | G/T | 0.030665 | 0.119967 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080841 | gtcttgaactcctga[G/T]cttgagccatcctcc | 672 |
rs8176189 | snp | C/T | 0.0110494 | 0.0735024 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080741 | acagctcactgcagc[C/T]tctcgacctcctcaa | 672 |
rs8176190 | snp | A/G | 0.246485 | 0.249975 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080681 | GCTGGGACTATAGGC[A/G]TCCACCACCATACCC | 672 |
rs8176191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080245 | tccttaattcttcac[A/G]ataccctgtacaatg | 672 |
rs8176192 | snp | C/G | 0.253264 | 0.249979 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079681 | AGCAGGCTGGTGCTT[C/G]AGTTGAACCCACGTA | 672 |
rs8176193 | snp | A/G | 0.457037 | 0.140127 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079499 | AGCATGCTGGGTCAC[A/G]TTGTAGACTTTTCCA | 672 |
rs8176194 | snp | G/T | 0.445855 | 0.155373 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079204 | CTCTGCCTTTCATTT[G/T]TTTTGTTTTGTTTTG | 672 |
rs8176195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078981 | aactcctgacctcag[A/G]tgatctgtccacctc | 672 |
rs8176196 | snp | C/T | 0.499982 | 0.00299515 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078973 | ACCTCAGGTGATCTG[C/T]CCACCTCGGCCTCTC | 672 |
rs8176197 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078965 | tgatctgtccacctc[A/G]gcctctcaaagtgct | 672 |
rs8176198 | snp | A/T | 0.499989 | 0.00239614 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078520 | TAATGAATAGAAGAC[A/T]TTTGCAATTTTTAAC | 672 |
rs8176199 | snp | A/C | 0.377977 | 0.21476 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078507 | ACTTTTGCAATTTTT[A/C]ACTATTTGTTTTTAC | 672 |
rs8176200 | snp | C/T | 0.44546 | 0.155869 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078359 | GGTGGCTCATGCCTA[C/T]AATCCCAGCACTTTG | 672 |
rs8176201 | snp | C/T | 0.44546 | 0.155869 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078319 | GGTTGGCGGATCACC[C/T]GAGGTCAGGAGTTTA | 672 |
rs8176202 | snp | C/T | 0.44546 | 0.155869 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078211 | CTATAATCCCATCTT[C/T]TTGGGAGGCTAAGGC | 672 |
rs8176203 | snp | A/G | 0.457154 | 0.139954 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077756 | ACAAGAGCAAACTCC[A/G]TCTCAAAAAAAATAA | 672 |
rs8176204 | snp | A/T | 0.457504 | 0.139435 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077746 | actccatctcaaaaa[A/T]aataaataaataaaa | 672 |
rs8176206 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076103 | ATAATAATAATTACT[A/G]TTATTATTATTTTTT | 672 |
rs8176207 | in-del | -/TTCC | 0.452978 | 0.145945 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075066 | CCTTTCTTTCTTCCT[-/TTCC]TTCCTTCCTTCCTTC | 672 |
rs8176209 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074861 | tgatctcggctcact[A/G]caacctctgtctccc | 672 |
rs8176210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074813 | ctgcctcagcctccc[A/G]agtagctgagattac | 672 |
rs8176211 | in-del | -/ACCCCA | 0.435362 | 0.167753 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074718 | CCTCAGACCAACCCA[-/ACCCCA]TGTTATATGTCAACC | 672 |
rs8176213 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074226 | TACTAGTCTATCATG[A/G]ACACTTTTGTTATAC | 672 |
rs8176214 | snp | A/G | 0.457853 | 0.138915 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073822 | GGTTGCGGTGAGCCA[A/G]GATCACACCACTGCA | 672 |
rs8176215 | snp | A/T | 0.472429 | 0.114129 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073766 | CTCCATCTCAAAAAA[A/T]ATATATATATATATA | 672 |
rs8176216 | snp | A/T | 0.442113 | 0.159977 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073764 | CCATCTCAAAAAATA[A/T]ATATATATATATATA | 672 |
rs8176217 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073750 | atatatatatatata[C/T]acacacatatatTTT | 672 |
rs8176218 | in-del | -/ACAAGCATTGTTACAGTGAACATT | 0.457737 | 0.139088 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071521 | taaaattatactatt[-/ACAAGCATTGTTACAGTGAACATT]CCTATGACTAAACCT | 672 |
rs8176219 | snp | A/G | 0.00338409 | 0.040995 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43071056 | GCTGCTGCTCATACT[A/G]CTGATACTGCTGGGT | 672 |
rs8176220 | snp | C/T | 0.45843 | 0.138046 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070445 | ACTTCTGCCCTGCAA[C/T]ATCCCTTGCTATTAG | 672 |
rs8176221 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070444 | CTTCTGCCCTGCAAT[A/T]TCCCTTGCTATTAGG | 672 |
rs8176222 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070082 | gccgggcgtggtggc[A/G]catgcctataatccc | 672 |
rs8176223 | snp | A/G | 0.0111728 | 0.0739025 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070019 | ttgaacccgggaggc[A/G]gaggttgcggtgagc | 672 |
rs8176224 | snp | A/G | 0.0121208 | 0.0768991 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069657 | TGCACAGTGATGGCT[A/G]TAAATGTTTTCATCT | 672 |
rs8176225 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069579 | GTGTCTGTTTCAATG[G/T]CTCTTGATCACTTGC | 672 |
rs8176226 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069161 | GTAGCAAAAGGGGGA[A/G]GATGTCATTAGCTTC | 672 |
rs8176227 | snp | C/G | 0.0111728 | 0.0739025 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069121 | CCTTTTTTCAGTGCC[C/G]TGTGGCAGTATGGAG | 672 |
rs8176228 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068303 | AAACTATTTATTTGA[G/T]ACTTCAGGTATCttt | 672 |
rs8176229 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068271 | ttttttttttgagac[A/G]gagtctcgcactctc | 672 |
rs8176230 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068255 | gagtctcgcactctc[A/G]cccaggctagagtgc | 672 |
rs8176231 | snp | C/T | 0.457969 | 0.138741 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068206 | TACTGCAAGCTCTGC[C/T]TCCTGGGTTCACGCC | 672 |
rs8176232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068006 | acaggcgtgagccac[C/T]gcgcccagccGAGAC | 672 |
rs8176233 | snp | A/G | 0.457737 | 0.139088 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43067787 | GTGCAGGATTGCTAC[A/G]TAGGTAAACATATGC | 672 |
rs8176234 | snp | A/G | 0.457737 | 0.139088 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43067763 | CATATGCCATGGTGG[A/G]ATAACTAGTATTCTG | 672 |
rs8176235 | snp | A/G | 0.425432 | 0.178112 | BRCA1 | 17 | allele_origin=G(germline)/A(somatic) | 17:43067543 | CATGAGGCGAGGCAC[A/G]GTGGCGCATGCCTGT | 672 |
rs8176236 | snp | C/T | 0.204189 | 0.245767 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066788 | GGTGGTGAGCTGAGA[C/T]AGTCAACTATTAACT | 672 |
rs8176237 | snp | A/G | 0.120326 | 0.21374 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066730 | TGAGGTGGAGCCTAA[A/G]TCCTAAAACAACAAG | 672 |
rs8176238 | snp | A/C/G | 0.0385278 | 0.134199 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066690 | tggacgcggtggctc[A/C/G]catcagtaatcccag | 672 |
rs8176239 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066409 | caacaaaagaaagaa[C/G/T]aaGTGAGGCAAAACC | 672 |
rs8176240 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066355 | ACCTAGTTTGAGTAT[C/T]GTTGAGAGTTTTTCA | 672 |
rs8176241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066187 | tgtttttagttgact[A/G]taaactaaatctgag | 672 |
rs8176242 | snp | A/G | 0.446118 | 0.155041 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065857 | gaagaaccgttaccc[A/G]gaagagaactgttat | 672 |
rs8176243 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065535 | CTGGGATTACAGGAA[G/T]GCACCACCATACCTA | 672 |
rs8176244 | snp | A/G | 0.030665 | 0.119967 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065497 | atttttagtagagac[A/G]gggtttttccatgtc | 672 |
rs8176245 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065363 | TTCTTTTCACAGAGA[C/T]ACAGGCACTTAAGGA | 672 |
rs8176246 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065094 | gcctgtaatcccagc[A/G]ctttggggggccaag | 672 |
rs8176248 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065086 | tcccagcgctttggg[A/G]ggccaaggcgggcag | 672 |
rs8176249 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065084 | ccagcgctttggggg[C/G]ccaaggcgggcagat | 672 |
rs8176250 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065024 | gctaacacggtgaaa[A/C]cccatctctagtaaa | 672 |
rs8176252 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064696 | GCAGTTAAACAAAAA[A/T]CTTCAAAAATTGTAA | 672 |
rs8176253 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064693 | GTTAAACAAAAAACT[A/T]CAAAAATTGTAAGGA | 672 |
rs8176254 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064327 | TCTTTCACATATTGC[C/T]ATCTAGTAATATAGA | 672 |
rs8176255 | snp | C/T | 0.203882 | 0.245709 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064324 | TTCACATATTGCCAT[C/T]TAGTAATATAGATGT | 672 |
rs8176256 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064189 | GAGAAGAGGGAGTGG[A/G]CAGATATTTCCTCTG | 672 |
rs8176257 | snp | A/C | 0.412583 | 0.189912 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064188 | AGAAGAGGGAGTGGA[A/C]AGATATTTCCTCTGG | 672 |
rs8176258 | snp | C/T | 0.0217236 | 0.101931 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43064004 | CTTCTTAGGACAGCA[C/T]TTCCTGATTTTGTTT | 672 |
rs8176259 | in-del | -/T | 0.0490535 | 0.14873 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43063789 | AACACCTAAGGTTTT[-/T]GCTGATGCTGAGTCT | 672 |
rs8176260 | snp | C/T | 0.000151122 | 0.00869127 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43063311 | ACTTGATGTTACAAA[C/T]TAACCAGAGATATTC | 672 |
rs8176261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063051 | aatacaaaattagcc[A/G]ggcttggtggcactt | 672 |
rs8176262 | snp | C/G | 0.0162591 | 0.0886858 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062464 | AGAACAAGAAGTGGG[C/G]CCACTTGCATATACC | 672 |
rs8176263 | in-del | -/TT | 0.43978 | 0.162738 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43062193 | AGCCAGAAGAATCAC[-/TT]GAGCCCAGGAGTTCA | 672 |
rs8176264 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062062 | TATACATATATATAC[A/G]TGCAAATGTATCTGT | 672 |
rs8176265 | snp | A/G | 0.438246 | 0.16451 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061979 | GTGAGAAGTAAATAA[A/G]ATAGAGTGTAGGAGG | 672 |
rs8176266 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061743 | acaaaaaaattagtc[A/G]agcgtggtggcatgt | 672 |
rs8176267 | snp | A/G | 0.148326 | 0.228391 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061731 | GTCGAGCGTGGTGGC[A/G]TGTGCCTGTAATCCT | 672 |
rs8176268 | snp | A/G | 0.450105 | 0.149859 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061643 | GTGAGCCTAGATTGC[A/G]CCACTGCACTCCAGC | 672 |
rs8176269 | snp | A/C | 0.438246 | 0.16451 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061609 | TGAGACAGAATGAGA[A/C]CCTGTCTTAAAAAAA | 672 |
rs8176270 | snp | C/T | 0.0112991 | 0.0743093 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061603 | agaatgagaccctgt[C/T]ttaaaaaaaaaaaaa | 672 |
rs8176271 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061557 | CTATTGTGCACAATT[C/T]GATGTATTCATAATT | 672 |
rs8176272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061347 | TATGGAGAAATATAC[A/G]GAACAGTGGAATAGT | 672 |
rs8176273 | snp | C/T | 0.438666 | 0.164028 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059636 | ACTTGGGTTTTGGCT[C/T]GAACAATAGATCTTG | 672 |
rs8176274 | snp | G/T | 0.00338409 | 0.040995 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059010 | AAATGTCAGATATTC[G/T]TCCCCTAGTAATAGC | 672 |
rs8176275 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058766 | TTATCATTTTGGTTG[G/T]GTTAACTGTAAATCT | 672 |
rs8176276 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058585 | TGAAAATTAAAATAC[A/G]TTAAGTCCCAGTGAG | 672 |
rs8176277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058409 | TTTCTTTCTTTCTTT[C/T]TTTTGTTTTATGTGT | 672 |
rs8176278 | snp | A/G | 0.254944 | 0.249951 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058399 | TCTTTTTTTTGTTTT[A/G]TGTGTGTGTGTGTGT | 672 |
rs8176279 | snp | G/T | 0.496681 | 0.0405994 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058379 | TGTGTGTGTGTGTGT[G/T]TTTTTTTAGCAGAGT | 672 |
rs8176280 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057610 | ctgacctcgtgatcc[G/T]cctgtctcggcctcc | 672 |
rs8176281 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057601 | tgatccgcctgtctc[A/G]gcctcccaaagtcct | 672 |
rs8176282 | snp | A/G | 0.450483 | 0.149354 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057561 | GGCGTGAGCCACCAC[A/G]CCCGGCCTAATTTTT | 672 |
rs8176283 | snp | A/G | 0.0115603 | 0.0751433 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057473 | cccaggctggagtgc[A/G]gtggcaccatctcag | 672 |
rs8176284 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056866 | AGTATTGTCTCTACT[C/T]TATGAATGATAAAAC | 672 |
rs8176285 | snp | C/G/T | 0.00279258 | 0.0372817 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056461 | ccaggcacagcggct[C/G/T]gttcctgttatccca | 672 |
rs8176286 | snp | C/T | 0.030665 | 0.119967 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056450 | ggctcgttcctgtta[C/T]cccagcactttggga | 672 |
rs8176287 | snp | A/G | 0.277867 | 0.248442 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054835 | gaatcggttgaaccc[A/G]ggaggcggaggttgc | 672 |
rs8176288 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054114 | AGTGCTTTGGATTTT[C/T]TCCTCCATGCAGAAT | 672 |
rs8176289 | snp | A/G | 0.450609 | 0.149185 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054039 | ATACTAAATGTCACC[A/G]TAGTATTTTTCTCTG | 672 |
rs8176290 | snp | C/T | 0.450483 | 0.149354 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053755 | CTTGAACTCCCGACC[C/T]CAAGTGATCCACCCA | 672 |
rs8176292 | snp | A/G | 0.0114282 | 0.0747228 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053620 | gagtgcagtggcgcc[A/G]tctcggctcactacc | 672 |
rs8176293 | in-del | -/A | 0.0217236 | 0.101931 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43053354 | ATTTCTTATCTCATA[-/A]CTAGGCATCCTCATC | 672 |
rs8176294 | snp | C/T | 0.0115603 | 0.0751433 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053080 | gaccagcctggccaa[C/T]atagtgaaaccccgt | 672 |
rs8176295 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052991 | TACTAGGGAGGCTGA[A/G]GCAGGAGAATCACTT | 672 |
rs8176296 | snp | A/G | 0.450609 | 0.149185 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051574 | TGTTGATGGGGTCAT[A/G]GTGAGTACTTGAGGT | 672 |
rs8176297 | snp | A/T | 0.450609 | 0.149185 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051308 | GATCTTCTGAAATCC[A/T]GTAGTGTTCTGGACA | 672 |
rs8176298 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050878 | TGGCAAAAAAAAACT[A/C]TACCTTGTCCCCCTT | 672 |
rs8176299 | snp | A/G | 0.0112991 | 0.0743093 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050424 | agacggggtttcacc[A/G]tgttagccaatatgg | 672 |
rs8176300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050278 | CTTAATACAATGTTA[C/T]GCTTAGGACTGCTAT | 672 |
rs8176301 | snp | A/C | 0.00343052 | 0.0412734 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050006 | TTTTTATGAAATTTC[A/C]AAGTTCCACTCAAGG | 672 |
rs8176302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049820 | AATGTCTTGAAGAAC[A/C]CAGCCAACAGAGCCC | 672 |
rs8176303 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049448 | TCTTTCAAGCATTTT[A/G]TTTGAGAGACTATCA | 672 |
rs8176304 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049415 | CCTTATACCAAGTGG[A/C]CTTATGGAGACTGAT | 672 |
rs8176305 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049347 | AAAATCCATACCCCT[A/G]CTATTTTAAGACCAT | 672 |
rs8176306 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049328 | TTTTAAGACCATTGT[A/C]CTTTGGAGCAGAGAG | 672 |
rs8176307 | snp | C/T | 0.0209421 | 0.100162 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43049053 | AGCAAGACTGGCACC[C/T]GTCAGTCCCTATGGA | 672 |
rs8176308 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048353 | tagctgggcgtaggg[G/T]cgcacgcctgtagtc | 672 |
rs8176310 | snp | A/G | 0.497695 | 0.0338674 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047896 | TAGTTCCAGCTACTT[A/G]GGAGGCTGAGATGGA | 672 |
rs8176311 | snp | A/G | 0.0110494 | 0.0735024 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047122 | acagagcgagaccgt[A/G]tctcaaaaagaaaaa | 672 |
rs8176312 | snp | A/G | 0.206642 | 0.246211 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047106 | tctcaaaaagaaaaa[A/G]gaaaGTATAAATTTA | 672 |
rs8176313 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046985 | TGTATTTTATAAAAT[A/G]TGATCATAATTACAC | 672 |
rs8176314 | snp | C/T | 0.450357 | 0.149522 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046604 | GACCAGCCTGGCCAA[C/T]ATGGCGAAACCCCAT | 672 |
rs8176315 | snp | A/G | 0.0143877 | 0.0835874 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046530 | cgcacttgtagtccc[A/G]gctacttgggagact | 672 |
rs8176316 | snp | A/C | 0.00281451 | 0.0374077 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43045812 | CTCTGCTTGTGTTCT[A/C]TGTCTCCAGCAATTG | 672 |
rs8176317 | snp | A/G | 0.00109409 | 0.0233634 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045406 | ATTTAAACGCCACCA[A/G]TTGAGCAAGATGCTG | 672 |
rs8176318 | snp | G/T | 0.494269 | 0.0532239 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045257 | CCCTGTGTTCACAAA[G/T]GCAGAGAGTCAGACC | 672 |
rs8176319 | snp | C/T | 0.00221811 | 0.0332285 | BRCA1 | 17 | allele_origin=T(unknown)/C(germline) | 17:43044897 | agaatcacttcagcc[C/T]gggaggtggaggttg | 672 |
rs8176320 | snp | A/G | 0.00994634 | 0.0698157 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044346 | TACAAAATACGTTTT[A/G]TAAATGTTGTGCTGT | 672 |
rs8176321 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044182 | gtatctacctcctag[A/G]attTATTGAGGCAGC | 672 |
rs9709315 | snp | A/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078038 | ctgcgcccgaccGtt[A/T]tttttcaacgagatg | 672 |
rs9889400 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43053062 | tttgtatttttagta[A/G]aaacggggtttcact | 672 |
rs9892009 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121698 | caaaaaaaaaaaaaa[A/C]aaaaaaaaaagaaaT | 672 |
rs9895855 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118338 | tctggtaggaaccta[C/T]aggctattttaaatc | 672 |
rs9896925 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046658 | ccgcccTgaggctga[A/G]gcaggagaatcattt | 672 |
rs9897397 | snp | A/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052825 | CACACACACACACAC[A/T]CTCTTACTTTACCGC | 672 |
rs9897466 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067806 | gcaatcctgcacgtt[C/T]tacacgtgtcctgga | 672 |
rs9898965 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101762 | ctgcctcagcctccc[A/G]aagtgctgggattac | 672 |
rs9899263 | snp | C/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077083 | TGGGGATTTCAGCTT[C/T]TGCATGTCGGGGGTA | 672 |
rs9913747 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087689 | aaaaaaaagaaaaaa[A/G]aaTTTTAATGATCCA | 672 |
rs9916146 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057960 | aggaggcagaggttg[C/T]tgtgagccacgatca | 672 |
rs10445302 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100680 | tatatatatatataa[A/T]atatatatatatata | 672 |
rs10445303 | snp | C/T | 0.457037 | 0.140127 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102388 | tttgagacggagtct[C/T]gctctgtcgccaggc | 672 |
rs10445316 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100558 | tatgtgtgtgtgtgt[A/G]tatatatatatataa | 672 |
rs10445317 | snp | A/T | 0.412416 | 0.190055 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100595 | tataacatatatata[A/T]tatatatatataaca | 672 |
rs10445318 | snp | A/C/T | 0.412416 | 0.190055 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100596 | ataacatatatatat[A/C/T]atatatatataacat | 672 |
rs10445319 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100679 | atatatatatatata[A/T]tatatatatatatat | 672 |
rs10445320 | snp | A/G | 0.457037 | 0.140127 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102157 | ctcactgcaagctcc[A/G]cctcccgggttcatg | 672 |
rs10445321 | snp | G/T | 0.495368 | 0.0478996 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102469 | tcaagtgattctcca[G/T]cctcagcctctggag | 672 |
rs10695721 | in-del | -/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114406 | TTTTTTTTTTTTTTT[-/T]GAGTCTCCCTCTTGT | 672 |
rs11079053 | snp | A/T | 0.0715223 | 0.175059 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050573 | agccgagatcgcgcc[A/T]ttgcactctggcctg | 672 |
rs11079054 | snp | C/G | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107808 | TCAAAGTGGATCATA[C/G]ACCAGAAGTAGAGAG | 672 |
rs11347376 | in-del | -/T | 0.490563 | 0.0680388 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054745 | TGTGCCCAGCTGGGA[-/T]TTTTTTTTTTTTTTT | 672 |
rs11368665 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077760 | TTTTTTGAGATGGAG[-/T]TTTGCTCTTGTTGCC | 672 |
rs11412754 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114087 | TCAAAAAAAAAAAAA[-/A]GACAGGGTCTCACTC | 672 |
rs11421283 | in-del | -/TT | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067847 | TTTTTTTTTTTTTTT[-/TT]AGACAGAGTCTTGGT | 672 |
rs11555992 | snp | G/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071042 | TACTGATACTGCTGG[G/T]TATAATGCAATGGAA | 672 |
rs11651194 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067472 | tgctggccaggatgg[G/T]ctcgatctcctaatc | 672 |
rs11651855 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110158 | ctcagcctcccaaag[C/T]gctgggattacaggc | 672 |
rs11652377 | snp | C/T | 0.438666 | 0.164028 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060152 | ctcagctcaccacaa[C/T]ctccacctcccgggt | 672 |
rs11654396 | snp | G/T | 0.37778 | 0.214877 | BRCA1 | 17 | allele_origin=G(germline)/T(somatic) | 17:43067324 | CAGTGGCATGATCTC[G/T]GCTCACTGCAACCTC | 672 |
rs11655505 | snp | A/G | 0.457388 | 0.139608 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126360 | CTAGTTACTGTCTTT[A/G]TCCGCCATGTTAGAT | 672 |
rs11655841 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044900 | cctccacctcccggg[C/G]tgaagtgattctcct | 672 |
rs11656377 | snp | A/G | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050618 | GACCTCAAAAAAAAA[A/G]AAAAAAAAAAAGAAA | 672 |
rs11657823 | snp | A/G | 0.445196 | 0.1562 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112129 | GAATCTTGCTCTGTC[A/G]CCCAGGCTAGAGTAC | 672 |
rs11658140 | snp | C/G | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052113 | ACACAGATCACACTG[C/G]ACTGCCTCTTCCACT | 672 |
rs11658785 | snp | A/C | 0.016932 | 0.0904395 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094764 | TACTTTTCTGGATGC[A/C]TCTCAGCTGCACGCT | 672 |
rs11658905 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095015 | AAGATGTAGCTCATA[A/C]TCTTTCATTTAATTC | 672 |
rs11658946 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095090 | ATTTCAGAATTTTCC[A/C]TATGCAGAAACCACA | 672 |
rs12150004 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100505 | tgcaactatgcctgg[A/C]taatttgtgtGTGTG | 672 |
rs12150042 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089269 | tgaaggttgcagtga[C/G]ccaaaattgtgccac | 672 |
rs12150520 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089254 | cctgaacctgggagc[C/T]gaaggttgcagtgag | 672 |
rs12450879 | snp | G/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056482 | ctgtgcctggcccag[G/T]gaacattatataaat | 672 |
rs12451607 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058045 | aaaaaaaaaaaaaaa[A/T]TTTAAGGCATTCAGA | 672 |
rs12601356 | snp | C/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114535 | AATTTAAATATAATT[C/T]TAGGAAATTCATAAA | 672 |
rs12936316 | snp | A/G | 0.456332 | 0.141164 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111027 | aatcacttgaaccag[A/G]gaggcagaggctgca | 672 |
rs12940378 | snp | C/T | 0.457271 | 0.139781 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077369 | GGAGTCTCACTCTGT[C/T]GCCCAAGCTGAAGTG | 672 |
rs12941007 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100670 | aacatatatatatat[A/G]tatatataatatata | 672 |
rs12941008 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100672 | catatatatatatat[A/G]tatataatatatata | 672 |
rs12941042 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123374 | ttttttttttttttt[G/T]gagatggagtttagc | 672 |
rs12943789 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073772 | tatatatatattttt[G/T]gagatggagtcttgc | 672 |
rs12946486 | snp | C/G/T | 0 | 0 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091519 | CTGAAACCAATTCCT[C/G/T]GTCACTCAGACCAAC | 672 |
rs12946839 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107299 | ccatctcctgacctc[A/G]tgatctgcccgcctc | 672 |
rs12947330 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059470 | gaacgagatgctgtc[A/T]caacaacaacaacaa | 672 |
rs12948474 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100598 | aacatatatatatta[C/T]atatatataacatat | 672 |
rs12949413 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107472 | tacaacctccacctc[A/C]taggctcaagcaatt | 672 |
rs12949768 | snp | A/G | 0.119978 | 0.213528 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050562 | AGGTTGCAGTGAGCC[A/G]AGATCGCGCCATTGC | 672 |
rs12950713 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073773 | atatatatatttttt[A/G]agatggagtcttgct | 672 |
rs17671533 | snp | C/T | 0.144969 | 0.226867 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052839 | TTCTTTTCACTCTGG[C/T]GGTAAAGTAAGAGAG | 672 |
rs28385359 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100691 | ATAATATATATATAT[A/G]TATATATATATGTAA | 672 |
rs28426973 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100689 | ATATAATATATATAT[A/G]TATATATATATATGT | 672 |
rs28744524 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107239 | CCGGCTAATTTTTTT[A/T]TTTTTAGTAGAGACG | 672 |
rs28897672 | snp | A/C/G/T | 0.000134438 | 0.00819762 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43106487 | AAAGGGCCTTCACAG[A/C/G/T]GTCCTTTATGTAAGA | 672 |
rs28897673 | snp | A/G | 0.000115642 | 0.00760314 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43104249 | CAGATGCAAACAGCT[A/G]TAATTTTGCAAAAAA | 672 |
rs28897674 | snp | A/C/G | 0.000115306 | 0.00759223 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43099865 | CAGGAAACCAGTCTC[A/C/G]GTGTCCAACTCTCTA | 672 |
rs28897675 | snp | G/T | 0.000436168 | 0.0147612 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43094795 | CCCAGTAATAATGAT[G/T]TGAACACCACTGAGA | 672 |
rs28897676 | snp | A/C/T | 0.000346012 | 0.0131486 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43094045 | CAGATAATACAAGAG[A/C/T]GTCCCCTCACAAATA | 672 |
rs28897677 | snp | A/G | 0.00093899 | 0.0216475 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094044 | AGATAATACAAGAGC[A/G]TCCCCTCACAAATAA | 672 |
rs28897678 | snp | A/G | 1.65097e-05 | 0.00287308 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093800 | ATCACTCGAAAAAGA[A/G]TCTGCTTTCAAAACG | 672 |
rs28897679 | snp | A/G | 0.00432589 | 0.0463058 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093560 | AAAAAAGTACAACCA[A/G]ATGCCAGTCAGGCAC | 672 |
rs28897680 | snp | A/C | 1.64806e-05 | 0.00287054 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43093471 | ACAAGCCAAATGAAC[A/C]GACAAGTAAAAGACA | 672 |
rs28897681 | snp | A/G/T | 0.00016484 | 0.00907733 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43093448 | AAAAGACATGACAGC[A/G/T]ATACTTTCCCAGAGC | 672 |
rs28897682 | snp | A/T | 0.000164804 | 0.00907607 | BRCA1 | 17 | allele_origin=T(germline,somatic)/A(germline) | 17:43093103 | TGTGCAGCATTTGAA[A/T]ACCCCAAGGGACTAA | 672 |
rs28897683 | snp | A/C | 0.000362474 | 0.0134575 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43093054 | ATAATAGAAATGACA[A/C]AGAAGGCTTTAAGTA | 672 |
rs28897684 | snp | A/G | 3.29636e-05 | 0.00405964 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093006 | TTAACCACAGTCGGG[A/G]AACAAGCATAGAAAT | 672 |
rs28897685 | snp | A/G | 0 | 0 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091947 | CTAGCCCTTTCACCC[A/G]TACACATTTGGCTCA | 672 |
rs28897686 | snp | A/G/T | 0.000527104 | 0.0162261 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43091783 | AGCACCGTTGCTACC[A/G/T]AGTGTCTGTCTAAGA | 672 |
rs28897687 | snp | G/T | 0.000477669 | 0.0154469 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43091823 | TGGTAAAGTAAACAA[G/T]ATACCTTCTCAGTCT | 672 |
rs28897688 | snp | C/G/T | 0.000329457 | 0.0128304 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43091818 | AAGTAAACAATATAC[C/G/T]TTCTCAGTCTACTAG | 672 |
rs28897689 | snp | A/G | 0.00792759 | 0.0624576 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091492 | TCAGATGATGAAGAA[A/G]GAGGAACGGGCTTGG | 672 |
rs28897690 | snp | A/G | 0.000176161 | 0.00938348 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43090997 | GAGAGTGAAACAAGC[A/G]TCTCTGAAGACTGCT | 672 |
rs28897691 | snp | A/C/G/T | 0.000362452 | 0.0134579 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43074370 | GAGTCTGGGCCACAC[A/C/G/T]ATTTGACGGAAACAT | 672 |
rs28897692 | snp | A/G | 8.23879e-05 | 0.00641772 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43074362 | GCCACACGATTTGAC[A/G]GAAACATCTTACTTG | 672 |
rs28897693 | snp | A/G | 0.00256667 | 0.0357316 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43071102 | ATTGAAAGTTCCCCA[A/G]TTGAAAGTTGCAGAA | 672 |
rs28897694 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070977 | CTTCAACAGAAAGGG[A/T]CAACAAAAGAATGTC | 672 |
rs28897695 | snp | C/G/T | 1.64754e-05 | 0.00287009 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43070929 | TGACCCCAGAAGAAT[C/G/T]TGTGAGTGTATCCAT | 672 |
rs28897696 | snp | A/C/T | 0.000116056 | 0.00761689 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43063903 | ATTTTCTAGGAATTG[A/C/T]GGGAGGAAAATGGGT | 672 |
rs28897697 | snp | A/G/T | 1.66646e-05 | 0.00288652 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43063369 | GATCTCTTTAGGGGT[A/G/T]ACCCAGTCTATTAAA | 672 |
rs28897698 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047685 | GTCCACCCAATTGTG[G/T]TTGTGCAGCCAGATG | 672 |
rs28897699 | snp | A/C/G | 0.0134222 | 0.0808143 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43045699 | GTGGCTGTGGGGGAT[A/C/G]TGGGGTATCAGGTAG | 672 |
rs34085552 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125987 | CAGTTATGGACTGGA[-/GT]GTGTTATGTTTTCGT | 672 |
rs34189929 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048019 | CTCAACTTCACCCCC[-/G]GGGATTATAGGCATG | 672 |
rs34191881 | in-del | -/A | | | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125354 | TGTCCCCCGTCCAGG[-/A]AAGTCTCAGCGAGCT | 672 |
rs34193078 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085234 | CCCTTAGTGCTCCAT[-/G]CCTGGCCATCACAGT | 672 |
rs34214126 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044517 | ATGGTTTCAGCAACA[-/G]GGGAGCAAAGGAAAA | 672 |
rs34250703 | in-del | -/AACCC | 0.44546 | 0.155869 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43074720 | GCCTCAGACCAACCC[-/AACCC]CATGTTATATGTCAA | 672 |
rs34253779 | in-del | -/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066813 | ACCACCCTCCAAACC[-/T]TTTTTTTTTTTTTTT | 672 |
rs34267863 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067255 | TCTTATTTTTTCACG[-/T]TTTTTTTTTTTTTTT | 672 |
rs34293035 | in-del | -/C | 0.434976 | 0.168179 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089551 | ATTGTGTACTTTCTT[-/C]TTTTTTTTTTTTTGA | 672 |
rs34399634 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076261 | TTTTTCTGACCTTCA[-/G]GAAGGGACATATCTA | 672 |
rs34485008 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071398 | GTAGCTTAGTTTCCT[-/A]AAAAGGAAATATGGC | 672 |
rs34545365 | snp | A/G | 0.000148247 | 0.00860822 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43099794 | ACAACCTCAAAAGAC[A/G]TCTGTCTACATTGAA | 672 |
rs34570933 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063343 | TTACCTCATTCAGCA[-/T]TTTTTCTTTCTTTAA | 672 |
rs34581553 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067803 | TAGCAATCCTGCACG[-/T]TTCTACACGTGTCCT | 672 |
rs34608699 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108336 | GAGTGAGATTGTGCC[-/A]AAAAAAAAAAAAAAG | 672 |
rs34613393 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067766 | AATACTAGTTATTCC[A/C]CCATGGCATATGTTT | 672 |
rs34685631 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052761 | GGTCACCCTCCCCCT[C/T]GACAGACAGACGGAC | 672 |
rs34725869 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092551 | CAGATTTTTCTTACA[-/T]TTTAGTTTTAACAAA | 672 |
rs34765977 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102706 | ATGATCACTCCACTG[C/T]ACTTCAGCGTGGGCG | 672 |
rs34770428 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097673 | GCTCAGCCACTTACT[-/A]AGGTTTAATACCTTG | 672 |
rs34869005 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095436 | ACCACAAAAAATTAA[-/C]CCGGGTGTGGTGGCA | 672 |
rs34941199 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071249 | CCCTCTGAAAGGAAT[-/G]GGGAGAAGTTTAATT | 672 |
rs34942571 | snp | C/G/T | 0.445724 | 0.155538 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121362 | TTTGAGACACGGTCT[C/G/T]GCTCTGCTGCCTAGG | 672 |
rs35064666 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123226 | CAGAGGTTTTTTTTT[A/T]ATATAGGATCTCTGT | 672 |
rs35119301 | snp | C/G | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123639 | AGGCATAAGCCACCG[C/G]CCTCGGCCTCATCCA | 672 |
rs35149296 | in-del | -/A | 0.489376 | 0.0721049 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115502 | GCGAGACTTTGTCTC[-/A]AAAAAAAAAAAAAAG | 672 |
rs35150209 | in-del | -/T | 0.361053 | 0.22398 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118761 | TTCTGAATGTGAACC[-/T]TTTTTTTTTTTTTTT | 672 |
rs35184764 | in-del | -/T | 0.494815 | 0.0506538 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078089 | AGGCTGGTTTCAAAC[-/T]TTTTTTTTTTTTTGA | 672 |
rs35202419 | in-del | -/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107063 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 672 |
rs35240258 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069129 | TGCCACAGGGCACTG[-/A]AAAAAGGCAGGCTAG | 672 |
rs35330014 | snp | C/T | 0.450357 | 0.149522 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060530 | GGAGTCTTGCTCTGT[C/T]GTTCAGGCTGGAGTG | 672 |
rs35436937 | in-del | -/T | | | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125385 | ACGCCGCGCAGTCGC[-/T]AGTTTTAATTTATCT | 672 |
rs35466763 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074906 | GCCTGAGTGACAGAG[-/C]CAAGACTCTGTCAAG | 672 |
rs35475366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060389 | ACCAGCCTGGCCAAC[A/G]TGGCAAAACCCCATC | 672 |
rs35484932 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099431 | TGTGCCACCACACCT[-/G]GGCTAATTTTTTATT | 672 |
rs35486643 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100903 | CTCTACTAAAAATAC[A/G]AAAATTAACTAGGCG | 672 |
rs35561635 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108706 | GGAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 672 |
rs35584960 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102357 | TTACAGGCGTGAAGC[-/T]TTTTTTTTTTTTTTT | 672 |
rs35635836 | in-del | -/AGGA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075085 | GGAAGGAAGGAAGGA[-/AGGA]AAGGAAGAAAGAAAG | 672 |
rs35668327 | snp | C/T | 0.456803 | 0.140473 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121078 | TGGACCTTTTTTTTT[C/T]GGGGTGGGGGGTTGG | 672 |
rs35682410 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108772 | TAATCCCAACACTTT[-/G]GGGAGAGGTCAGGAG | 672 |
rs35688186 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108083 | TGCACGGTGGTCCAC[A/C]CCTGTAATCCCAGCA | 672 |
rs35693790 | in-del | -/T | 0.456568 | 0.140818 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098661 | ATGAGCCACCGCACC[-/T]GGCCAAAAATGTATT | 672 |
rs35771473 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098030 | TGAGCTCAGCAGCTC[-/T]TTTTTTTTTTTTTTT | 672 |
rs35805899 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050609 | CAGAGACTCGACCTC[-/A]AAAAAAAAGAAAAAA | 672 |
rs35851659 | in-del | -/T/TT | 0.496483 | 0.0417852 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114390 | TTTTTTTTTTTTTTT[-/T/TT]GAGTCTCCCTCTTGT | 672 |
rs35908185 | snp | A/T | 0.45692 | 0.1403 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103094 | TTCCAAATGCTTAAA[A/T]ATATCAGTGACCTTA | 672 |
rs35919712 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111541 | AACAAAAAAAAACAG[-/C]CCGGGCGTGGTGGCT | 672 |
rs35935832 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089607 | GGCTGGAGAGCAGCA[G/T]CATGATCTCAGCTCA | 672 |
rs35981190 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107735 | TGAGACAAAAGTATA[A/T]CCACATGTAAAAGAA | 672 |
rs35999570 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091850 | ACCAAATAACAAGTG[-/T]TGGAAGCAGGGAAGC | 672 |
rs36039988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090744 | TCACACACACGCACA[C/T]GCGCACACACAGCCT | 672 |
rs36085989 | in-del | -/T | 0.456332 | 0.141164 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102948 | ACGGCACCCAGCTAC[-/T]TTTTTTTTTTTTTTA | 672 |
rs36086436 | snp | G/T | 0.456803 | 0.140473 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121520 | ATTTTGTATTTTTAG[G/T]AGAGACAGGGTTTCT | 672 |
rs36113921 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055643 | TACAAAAAACTATCT[C/T]GGTGTGGTGGCACGT | 672 |
rs36221744 | snp | C/T | 0.031825 | 0.122064 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126716 | CTCTCGGCGCCTCCT[C/T]GGCCTTGGCGTCCAT | 672 |
rs36221749 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127037 | AGGGCGGCTGGGGCC[C/T]GGTGAGAATTCAAGC | 672 |
rs41286288 | snp | C/T | 0 | 0 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099868 | TAGCAGGAAACCAGT[C/T]TCAGTGTCCAACTCT | 672 |
rs41286290 | snp | A/C/T | 3.29473e-05 | 0.00405864 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43094530 | ATGATAGGCGGACTC[A/C/T]CAGCACAGAAAAAAA | 672 |
rs41286292 | snp | A/G | 0.000378853 | 0.013758 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094466 | AAAAGAATGGAATAA[A/G]CAGAAACTGCCATGC | 672 |
rs41286294 | snp | C/G/T | 6.61106e-05 | 0.00574905 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43093997 | AGACCTACATCAGGC[C/G/T]TTCATCCTGAGGATT | 672 |
rs41286296 | snp | A/G/T | 0 | 0 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43093268 | CTCATGTTAAGTGGA[A/G/T]AAAGGGTTTTGCAAA | 672 |
rs41286298 | snp | A/G | 0.000148335 | 0.00861078 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093163 | TTACTGGAAGTTAGC[A/G]CTCTAGGGAAGGCAA | 672 |
rs41286300 | snp | C/T | 0.000197788 | 0.00994258 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092935 | TTCAAGGTTTCAAAG[C/T]GCCAGTCATTTGCTC | 672 |
rs41293445 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092320 | GAAAACATTCAAGCA[A/G]AACTAGGTAGAAACA | 672 |
rs41293447 | snp | A/G | 0.000313482 | 0.0125157 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092229 | AAAGTCTTCCTGGAA[A/G]TAATTGTAAGCATCC | 672 |
rs41293449 | snp | A/C/G | 0.00018176 | 0.00953136 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43092204 | GCATCCTGAAATAAA[A/C/G]AAGCAAGAATATGAA | 672 |
rs41293451 | snp | C/T | 6.59065e-05 | 0.00574012 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091840 | TTCCAACACTTGTTA[C/T]TTGGTAAAGTAAACA | 672 |
rs41293453 | snp | A/G | 6.58979e-05 | 0.00573974 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43082516 | AATGGCTGAACTAGA[A/G]GCTGTGTTAGAACAG | 672 |
rs41293455 | snp | C/G/T | 8.23765e-05 | 0.00641738 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43082434 | GCCCTTGAGGACCTG[C/G/T]GAAATCCAGAACAAA | 672 |
rs41293457 | snp | C/G | 0.000115324 | 0.00759268 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43074381 | AACAGCTGGAAGAGT[C/G]TGGGCCACACGATTT | 672 |
rs41293459 | snp | A/C/G/T | 4.98708e-05 | 0.00499328 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063930 | AGTTTGTGTGTGAAC[A/C/G/T]GACACTGAAATATTT | 672 |
rs41293461 | snp | A/C/G | 0 | 0 | stop-gained, missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063373 | CTATGATCTCTTTAG[A/C/G]GGTGACCCAGTCTAT | 672 |
rs41293463 | snp | A/G/T | 0 | 0 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43051071 | GGCCCTTCACCAACA[A/G/T]GCCCACAGGTAAGAG | 672 |
rs41293465 | snp | C/T | 0 | 0 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43045767 | GCACCTGTGGTGACC[C/T]GAGAGTGGGTGTTGG | 672 |
rs45444999 | snp | A/G | 0 | 0 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43063882 | GAAAATGGGTAGTTA[A/G]CTATTTCTGTAAGTA | 672 |
rs45456891 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104084 | TCTTCTTCTTCTTCT[C/T]TTCTTTTTTTTTTCT | 672 |
rs45471406 | snp | A/G | 5.00872e-05 | 0.00500411 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43063386 | TAACCTGTCTTTTCT[A/G]TGATCTCTTTAGGGG | 672 |
rs45489593 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104081 | TCTTCTTCTTCTTTT[C/T]TTTTTTTTTTCTTTT | 672 |
rs45518438 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063521 | AACTGCTGCTACAAG[A/C]CTTATTAAAGGGCTG | 672 |
rs45519437 | snp | A/G | 4.98128e-05 | 0.00499038 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43063926 | TGTGTGTGAACGGAC[A/G]CTGAAATATTTTCTA | 672 |
rs45528433 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105154 | TTAGGCATTTGGTAG[A/G]CTTAAATGAATGACA | 672 |
rs45553935 | snp | C/G/T | 0 | 0 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43057122 | AGCATGATTTTGAAG[C/G/T]CAGAGGAGATGTGGT | 672 |
rs45564238 | snp | A/G | 0.00199806 | 0.0315443 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093682 | AGGAGGAAGTCTTCT[A/G]CCAGGCATATTCATG | 672 |
rs45569832 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104086 | CTTCTTCTTCTTCTT[C/T]TTTTCTTTTTTTTTT | 672 |
rs45586033 | snp | A/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094562 | TAACAGATGGGCTGG[A/T]AGTAAGGAAACATGT | 672 |
rs45599040 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092215 | AGTAATTGTAAGCAT[C/T]CTGAAATAAAAAAGC | 672 |
rs45620639 | snp | A/G | 0.00056563 | 0.0168076 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091399 | TGTTTGCCCCAGTCT[A/G]TTTATAGAAGTGAGC | 672 |
rs55633264 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049498 | ATTTCCATTAATTTG[C/T]TAAATTGCTGGCTAA | 672 |
rs55639854 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091500 | AATTGGTTTCAGATG[A/G]TGAAGAAAGAGGAAC | 672 |
rs55650082 | snp | A/G/T | 0.000115627 | 0.00760264 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43093742 | AGCAATATGGAACTC[A/G/T]AATTAAATATCCACA | 672 |
rs55678461 | snp | C/G | 0.000115383 | 0.00759462 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43093557 | AAAGTACAACCAAAT[C/G]CCAGTCAGGCACAGC | 672 |
rs55680227 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125086 | CCCTTCCTGATCCTC[A/C]GCGCTTCCCTCGCGA | 672 |
rs55680408 | snp | A/G | 3.46194e-05 | 0.00416035 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43095875 | CTCAAGGAACCAGGG[A/G]TGAAATCAGTTTGGA | 672 |
rs55685838 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111784 | CCGAGACTGCACCAC[C/T]GCACTCCAGCCTGGG | 672 |
rs55688530 | snp | A/C/T | 0.00188389 | 0.0306333 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43097280 | TTTTAGGATCTGATT[A/C/T]TTCTGAAGATACCGT | 672 |
rs55720177 | snp | A/G | 0.000559993 | 0.0167237 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094104 | TCCCCAACTTAAGCC[A/G]TGTAACTGAAAATCT | 672 |
rs55725337 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091930 | ACACATTTGGCTCAG[A/G]GTTACCGAAGAGGGG | 672 |
rs55737636 | snp | C/T | 0.499942 | 0.00539106 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112722 | CTGACTATCACAATC[C/T]TGACTATCACAAGCT | 672 |
rs55746541 | snp | A/C/G | 0.000115372 | 0.00759424 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43093119 | TAAATGTGTGAGTCA[A/C/G]TGTGCAGCATTTGAA | 672 |
rs55767801 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094609 | GAATTCTGTAATAAA[A/G]GCAAACAGCCTGGCT | 672 |
rs55770810 | snp | A/C/T | 8.31187e-05 | 0.00644622 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43063931 | GAGTTTGTGTGTGAA[A/C/T]GGACACTGAAATATT | 672 |
rs55771949 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051433 | GCTCCTCCCTAATGA[A/T]CTCTGCAGGTGCTTT | 672 |
rs55790327 | in-del | -/TTAAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43091331 | TAAGAAGCAGTTCCT[-/TTAAC]TATACTTGGAAATTT | 672 |
rs55808233 | snp | C/T | 0.000346549 | 0.0131588 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43049179 | ATCAACTGGAATGGA[C/T]GGTACAGCTGTGTGG | 672 |
rs55809351 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071752 | CTCACACCTGTAATC[C/T]CAGCACTTTGGGAGG | 672 |
rs55815649 | snp | A/G | 0.00102096 | 0.0225708 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43074406 | ATTAAGGTTGTTGAT[A/G]TGGAGGAGCAACAGC | 672 |
rs55816927 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099838 | TCTAACCTTGGAACT[C/G]TGAGAACTCTGAGGA | 672 |
rs55820479 | in-del | -/GA | 0.499946 | 0.00519141 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112724 | GACTATCACAATCCT[-/GA]CTATCACAAGCTTGA | 672 |
rs55834099 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044789 | CTTTTAGAAATCTCT[C/T]CTAGTTTCATTTTCC | 672 |
rs55842957 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094516 | CCCAGCACAGAAAAA[A/G]AGGTAGATCTGAATG | 672 |
rs55848034 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091014 | AAGCAGCATCTGGGT[A/G]TGAGAGTGAAACAAG | 672 |
rs55851803 | snp | A/G | | | missense, splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43106477 | CACAGTGTCCTTTAT[A/G]TAAGAATGATATAAC | 672 |
rs55865150 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050984 | CTGAGGAACCCCCAT[C/T]GTGGGATCTTGCTTA | 672 |
rs55874646 | snp | A/G | 8.23649e-05 | 0.00641683 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094585 | CCTGGCTTAGCAAGG[A/G]GCCAACATAACAGAT | 672 |
rs55875201 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051213 | CAAAAAACAGACTTT[-/C]AAAAAGGAAGAGCTT | 672 |
rs55893499 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074036 | TACTGGGATTACAGG[C/T]GTGAGCCACTATGCC | 672 |
rs55906931 | snp | A/C/T | 0.000592963 | 0.0172084 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43094075 | CTAATTATAGGAGCA[A/C/T]TTGTTACTGAGCCAC | 672 |
rs55909400 | snp | C/G | 3.30224e-05 | 0.00406326 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43092185 | CAAGAATATGAAGAA[C/G]TAGTTCAGACTGTTA | 672 |
rs55914168 | snp | C/T | 0.000329576 | 0.0128327 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093180 | CTCAGGAAAGTATCT[C/T]GTTACTGGAAGTTAG | 672 |
rs55930959 | snp | A/G | 0.000115895 | 0.00761144 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091923 | TGGCTCAGGGTTACC[A/G]AAGAGGGGCCAAGAA | 672 |
rs55932871 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093559 | AAAAAGTACAACCAA[A/G]TGCCAGTCAGGCACA | 672 |
rs55946644 | snp | C/T | 0.00308657 | 0.0391632 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43049113 | TTGGCACAGTAAGTA[C/T]TGGGTGCCCTGTCAG | 672 |
rs55971303 | snp | A/C | 9.88517e-05 | 0.00702966 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43104138 | TTCTACAGAGTGAAC[A/C]CGAAAATCCTTCCTT | 672 |
rs55974475 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106131 | CTTAAAAAAAAAAAA[A/G]AAAAGAAAAGGAAAC | 672 |
rs55975699 | snp | A/G | 1.98482e-05 | 0.00315019 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094837 | GAATTTTCTGAGACG[A/G]ATGTAACAAATACTG | 672 |
rs55979584 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111768 | TGGAGCTTGCAGTGA[C/G]CCGAGACTGCACCAC | 672 |
rs56012641 | snp | A/C | 0.000545162 | 0.016501 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43093883 | GTGATGAATATTACT[A/C]ATAGTGGTCATGAGA | 672 |
rs56034136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063739 | TTAAAGATAAAAGTA[C/G]TTTAGTATTACAATT | 672 |
rs56039126 | snp | C/T | 9.89952e-05 | 0.00703476 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093666 | CCAGGCATATTCATG[C/T]GCTTGAACTAGTAGT | 672 |
rs56046357 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094148 | TGAAGACAAAATATT[A/T]GGGAAAACCTATCGG | 672 |
rs56051266 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093000 | ACAGTCGGGAAACAA[A/G]CATAGAAATGGAAGA | 672 |
rs56055578 | snp | A/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104174 | TCCAAAGTATGGGCT[A/G/T]CAGAAACCGTGCCAA | 672 |
rs56056327 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044787 | GACTTTTAGAAATCT[C/T]TTCTAGTTTCATTTT | 672 |
rs56056711 | snp | A/G | 1.6477e-05 | 0.00287024 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094426 | CCTAGAGATACTGAA[A/G]ATGTTCCTTGGATAA | 672 |
rs56082113 | snp | A/G | 0.0205511 | 0.0992634 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093073 | ATTCATGGTTGTTCC[A/G]AAGATAATAGAAATG | 672 |
rs56100707 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093990 | CATCAGGCCTTCATC[C/G]TGAGGATTTTATCAA | 672 |
rs56108540 | snp | C/T | 0.000515243 | 0.0160423 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045450 | TCTCAGGTGAAAAAT[C/T]ACCATAATTTTGTGC | 672 |
rs56119278 | snp | C/T | 0.000249545 | 0.0111674 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43071223 | AGGGAACCCCTTACC[C/T]GGAATCTGGAATCAG | 672 |
rs56119900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082296 | AATTACCCATGTGCT[A/G]AGCAAGGATCATAAA | 672 |
rs56128296 | snp | G/T | 0.00088943 | 0.0210695 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43094394 | ACTAAATAGCAGCAT[G/T]CAGAAAGTTAATGAG | 672 |
rs56131654 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050999 | CGTGGGATCTTGCTT[A/G]TAATACTCCACTATG | 672 |
rs56158747 | snp | A/C/T | 0.000801155 | 0.0199986 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43071232 | TCCTTTCAGAGGGAA[A/C/T]CCCTTACCTGGAATC | 672 |
rs56187033 | snp | A/G | 0.000543465 | 0.0164753 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43099786 | AAAAGACGTCTGTCT[A/G]CATTGAATTGGGTAA | 672 |
rs56195342 | snp | A/G | 0.000183252 | 0.0095704 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43063368 | ATCTCTTTAGGGGTG[A/G]CCCAGTCTATTAAAG | 672 |
rs56203716 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074682 | AGAAGTCTGGATTCA[C/T]GTTGCCTGCCAATAT | 672 |
rs56209245 | in-del | -/TAAAG | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124196 | TTTATCATTTTAAAA[-/TAAAG]TAAATTTAAGATTTG | 672 |
rs56214134 | snp | C/G/T | 0.000712271 | 0.0188591 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43091931 | TACACATTTGGCTCA[C/G/T]GGTTACCGAAGAGGG | 672 |
rs56272539 | snp | A/G | 0.000399281 | 0.0141238 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094020 | CAAATAAATTAAAGC[A/G]TAAAAGGAGACCTAC | 672 |
rs56295923 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076025 | TTGAGCCTGAAAAAC[A/G]GAGGATGCAGTGAGC | 672 |
rs56300722 | in-del | -/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102962 | CTTTTTTTTTTTTTT[-/T]AATTGCAGAGACAGT | 672 |
rs56310439 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094814 | AAATACTGAACATCA[G/T]CAACCCAGTAATAAT | 672 |
rs56321129 | snp | A/C/G | 0.000429007 | 0.0146397 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43092509 | TTTGAGGAACATTCA[A/C/G]TGTCACCTGAAAGAG | 672 |
rs56328013 | snp | A/C/G/T | 0.000627563 | 0.0177044 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43115792 | TTCTTTTTCTCCCCC[A/C/G/T]CTACCCTGCTAGTCT | 672 |
rs56329598 | snp | A/G/T | 1.64846e-05 | 0.0028709 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43093316 | AAACTAGAAACAGTT[A/G/T]AAGTGTCTAATAATG | 672 |
rs56335406 | snp | A/C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074501 | CCCCTTCTAAATGCC[A/C/T]ATCATTAGATGATAG | 672 |
rs56336919 | snp | A/G | 0.000181733 | 0.00953065 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091990 | GTTTTTAGCAAAAGC[A/G]TCCAGAAAGGAGAGC | 672 |
rs56337717 | snp | C/T | | | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044042 | CTCTAGAAGGGAACA[C/T]GCCCTGCGAACACCT | 672 |
rs56679756 | in-del | -/AT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100701 | TATATATATATATAT[-/AT]GTAATCCCAGCACTT | 672 |
rs56780197 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067977 | TACATTTAAAAAATT[A/C]TAAGACACCTGAAGT | 672 |
rs56914599 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079804 | AAAAAAAAAAAAAAA[-/A]GACCTTTGGACTGTA | 672 |
rs57489305 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108349 | CAAAAAAAAAAAAAA[-/A]GGCATTGGGAATTGT | 672 |
rs58091583 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113932 | ATACAAAAATTAGCT[C/G]GGTGTGGTGGCAGAT | 672 |
rs58834874 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113994 | GCAGGAGAATCGCTT[A/G]AACCCAGGAGGTGGA | 672 |
rs58891786 | in-del | -/ACCTACCTATCTATCT | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109067 | CCTACCTATCTATCT[-/ACCTACCTATCTATCT]GTCTACAGTCTTGAA | 672 |
rs59232370 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113986 | AGGCTGAGGCAGGAG[A/G]ATCGCTTGAACCCAG | 672 |
rs59278478 | in-del | -/ACACTC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052821 | CACACACACACACAC[-/ACACTC]TCTTACTTTACCGCC | 672 |
rs60259907 | in-del | -/GTTCACTGTAACAATGCTTGTAAT | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071524 | TTTAGTCATAGGAAT[-/GTTCACTGTAACAATGCTTGTAAT]AGTATAATTTTAGAA | 672 |
rs60667099 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113975 | AGCTACTCAAGAGGC[C/T]GAGGCAGGAGAATCG | 672 |
rs60735548 | in-del | -/CAA | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059470 | CAACAACAACAACAA[-/CAA]ATTCTCACATCTAAA | 672 |
rs60834728 | in-del | -/CA/CACA/CACACA | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086148 | ACACACACACACACA[-/CA/CACA/CACACA]GAAGTCCCCACCAAT | 672 |
rs60853932 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113976 | GCTACTCAAGAGGCT[A/G]AGGCAGGAGAATCGC | 672 |
rs60879064 | in-del | -/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064848 | TTTTTTTTTTTTTTT[-/T]GAGATGCAGTCTTGC | 672 |
rs60997700 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113967 | GTAATCCCAGCTACT[C/T]AAGAGGCTGAGGCAG | 672 |
rs61033980 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114024 | AGGTTGCAGTGAGCC[A/G]AGATCACACCACTGC | 672 |
rs61461583 | in-del | -/A | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119277 | CCATCTCAAAAAAAG[-/A]AAAAAAAAAAAGAAA | 672 |
rs61651289 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114023 | GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG | 672 |
rs62076408 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055445 | TGGAGGCCAGGAGAT[A/C]AAGGCCAGCCTGGCC | 672 |
rs62076409 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056673 | GTGAGACTCCGTCTT[A/G]GGAAAAAAAAAAAGA | 672 |
rs62076410 | snp | A/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062599 | CCTGGTTTGCGCTGC[A/T]AAATTTTTTTTTTTT | 672 |
rs62076411 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087914 | TTTTTTTTTTTTTCC[C/T]AGACAGGGGTTGCCC | 672 |
rs62076412 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098237 | GGTCTTGCTATGTTG[A/C]CCAGGCTGGTCTCAA | 672 |
rs62076413 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121714 | AAAAAAAAAAGAAAT[A/T]AATCTTAACAGGAAA | 672 |
rs62625285 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099844 | CAACTCTCTAACCTT[A/G]GAACTGTGAGAACTC | 672 |
rs62625298 | snp | A/G/T | 8.00849e-05 | 0.0063274 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43094838 | TGAATTTTCTGAGAC[A/G/T]GATGTAACAAATACT | 672 |
rs62625299 | snp | A/G | 0.000696113 | 0.0186433 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094766 | GAAGCGTGCAGCTGA[A/G]AGGCATCCAGAAAAG | 672 |
rs62625300 | snp | C/T | 1.64779e-05 | 0.00287031 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094150 | ATTGAAGACAAAATA[C/T]TTGGGAAAACCTATC | 672 |
rs62625301 | snp | C/T | 1.64776e-05 | 0.00287028 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094140 | AAATATTTGGGAAAA[C/T]CTATCGGAAGAAGGC | 672 |
rs62625303 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094060 | TTTGTTACTGAGCCA[C/T]AGATAATACAAGAGC | 672 |
rs62625304 | snp | A/G | 3.29995e-05 | 0.00406185 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094023 | TCACAAATAAATTAA[A/G]GCGTAAAAGGAGACC | 672 |
rs62625305 | snp | C/T | 0.000214283 | 0.0103487 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093620 | CCCACCTAATTGTAC[C/T]GAATTGCAAATTGAT | 672 |
rs62625306 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093142 | GGGAAGGCAAAAACA[A/G/T]AACCAAATAAATGTG | 672 |
rs62625307 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091933 | CATACACATTTGGCT[C/T]AGGGTTACCGAAGAG | 672 |
rs62625308 | snp | C/G/T | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=G(inherited)/T(inherited)/C(germline) | 17:43091924 | TTGGCTCAGGGTTAC[C/G/T]GAAGAGGGGCCAAGA | 672 |
rs66463208 | in-del | -/TG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100545 | ATATATACATATATA[-/TG]TGTGTGTGTGTGTAT | 672 |
rs66499067 | snp | C/G | 0.44546 | 0.155869 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096467 | GTCCCAGCTACTCGT[C/G]AGATTGAGACAGGAG | 672 |
rs66524247 | in-del | -/AT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100575 | TATATATATATAACA[-/AT]TATATATAACATATA | 672 |
rs66792711 | in-del | -/AAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100655 | ATATAACATATATAT[-/AAC]ATATATATATATATA | 672 |
rs67060599 | snp | A/G | 0.445724 | 0.155538 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103085 | TGAAGTAATTTCCAA[A/G]TGCTTAAAAATATCA | 672 |
rs67109310 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100678 | TATATATATATATAT[-/A]ATATATATATATATA | 672 |
rs67177158 | in-del | -/GAAAC | 0.499984 | 0.00279548 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112739 | GACTATCACAAGCTT[-/GAAAC]CAAGCTTCTCACTCT | 672 |
rs67242330 | in-del | -/GAGT | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052823 | GGCGGTAAAGTAAGA[-/GAGT]GTGTGTGTGTGTGTG | 672 |
rs67284603 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094522 | ATCTACCTTTTTTTC[-/T]TGTGCTGGGAGTCCG | 672 |
rs67906350 | in-del | -/T | 0.375 | 0.216506 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048688 | CCTGGCTACTTTTTG[-/T]TTTTTTTTTTTTAGT | 672 |
rs68106056 | in-del | -/A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058045 | AAAAAAAAAAAAAAA[-/A/T]TTTAAGGCATTCAGA | 672 |
rs68171917 | in-del | -/T | 0.430285 | 0.173197 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077335 | TCTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC | 672 |
rs70953658 | snp | A/C/G | | | synonymous-codon, missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091538 | TCAGTCTGAAAGCCA[A/C/G]GGAGTTGGTCTGAGT | 672 |
rs70953659 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074396 | TTGATGTGGAGGAGC[A/G]ACAGCTGGAAGAGTC | 672 |
rs70953660 | snp | C/T | 0.000428202 | 0.0146259 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43071074 | GAATCTGCCCAGAGT[C/T]CAGCTGCTGCTCATA | 672 |
rs70953661 | snp | C/G/T | 4.94181e-05 | 0.00497057 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43070980 | CAGCTTCAACAGAAA[C/G/T]GGTCAACAAAAGAAT | 672 |
rs71157698 | in-del | -/A | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046247 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 672 |
rs71157702 | in-del | -/TT | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067891 | AACTGGTATTCTATT[-/TT]TTTTTTTTTTTTTTT | 672 |
rs71160005 | in-del | -/TTTTTTTTTT | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096394 | TTCTTTCTTTCTCTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 672 |
rs71160008 | in-del | -/AAAAAAAA | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102375 | GCAAGACTCCGTCTC[-/AAAAAAAA]AAAAAAAAAAAAAAA | 672 |
rs71160013 | in-del | -/TTTT | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121708 | GTTAAGATTAATTTC[-/TTTT]TTTTTTTTTTTTTTT | 672 |
rs71228776 | in-del | -/GGA | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095107 | GACGTTAGAGAAATA[-/GGA]GGTGTGGTTTCTGCA | 672 |
rs71359598 | in-del | -/A | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046773 | AAAAAAAAAAAAAAA[-/A]GGCAATGCTTCAGGA | 672 |
rs71359599 | in-del | -/AAGG | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075084 | AGGAAGGAAGGAAGG[-/AAGG]AAAGGAAGAAAGAAA | 672 |
rs71359600 | in-del | -/GAA | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090061 | AGGGAAAAAAAAAAA[-/GAA]GAAGAGAAAGAAGTA | 672 |
rs71359601 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098031 | GAGCTCAGCAGCTCT[-/T]TTTTTTTTTTTTTTT | 672 |
rs71359602 | in-del | -/A | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108740 | AAAAAAAGGCCAGGA[-/A]GCGGTGGCTCACGCC | 672 |
rs71361503 | in-del | -/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108775 | TCCCAACACTTTGGG[-/G]AGAGGTCAGGAGTTC | 672 |
rs71361504 | in-del | -/GTT | 0.5 | 0 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125989 | ATGGACTGGAGTGTT[-/GTT]ATGTTTTCGTATTTT | 672 |
rs71367983 | snp | A/G | 0.375 | 0.216506 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100556 | TATATGTGTGTGTGT[A/G]TGTATATATATATAT | 672 |
rs71379207 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067380 | CTGCCTCAGCCTCAC[A/G]AGTAGCTGGGACTAC | 672 |
rs71989833 | in-del | -/TTTTC | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113373 | TTTTTCCTGGATGTA[-/TTTTC]TTTTCTTTTCTTTTT | 672 |
rs72370469 | in-del | -/TCTTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113366 | TTCCTGGATGTATTT[-/TCTTT]TCTTTTCTTTTTTTT | 672 |
rs72424527 | in-del | -/TA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100582 | ATATAACATATATAT[-/TA]AACATATATATATTA | 672 |
rs72434991 | in-del | -/A | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104063 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAGAAA | 672 |
rs72540131 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098660 | CATGAGCCACCGCAC[-/T]CGGCCAAAAATGTAT | 672 |
rs73311445 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048825 | GCCCAGCCTCCAGCC[C/T]ATCATTTCTTGATGA | 672 |
rs73321427 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110694 | AAAAAAGTATTACAG[C/G]CTGGGTGCGGTGGCT | 672 |
rs73321445 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119034 | ACCGGGATTACAGGC[A/G]TGAGCCACTACACTT | 672 |
rs73625094 | snp | C/G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125836 | TCCAGCATGCGTTGC[C/G/T]GAATGAAAGGTCTTC | 672 |
rs73625095 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125981 | TTGTCAACAGTTATG[A/G]ACTGGAGTGTTATGT | 672 |
rs73983787 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074488 | GTGCATGTACCACCT[A/G]TCATCTAATGATGGG | 672 |
rs73983788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106619 | ATAGCCATGAAAAGA[G/T]AATCTCACAACTGCC | 672 |
rs74268073 | in-del | -/AAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079802 | TTAAAAAAAAAAAAA[-/AAA]GACCTTTGGACTGTA | 672 |
rs74406523 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052217 | TAGCCATGAGTCACA[C/T]ATAGTTATTGAGCAC | 672 |
rs74588497 | snp | G/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112108 | ACTTTTTTTTTTTTT[G/T]AGACGGAATCTTGCT | 672 |
rs74598097 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103466 | AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 672 |
rs74627056 | snp | G/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112107 | GACTTTTTTTTTTTT[G/T]GAGACGGAATCTTGC | 672 |
rs74877299 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073428 | ATTAAGCATAGCTAA[A/G]TAGAATGTATGAGAT | 672 |
rs75071860 | snp | A/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098526 | ACCACACCCAGCTAA[A/T]TTTTTTTTTTTTTTG | 672 |
rs75129942 | snp | A/G | 0.0333488 | 0.124749 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110532 | TCAAGGCAACAGTAA[A/G]CCTCATGATCGCACC | 672 |
rs75184889 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098031 | TGAGCTCAGCAGCTC[C/T]TTTTTTTTTTTTTTT | 672 |
rs75240975 | snp | C/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055004 | ATCCACCCGCCTTGG[C/G]CTCCCAAAGTGCTGG | 672 |
rs75370952 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118395 | TTTCTTTTTTTTTTT[C/T]AGACAGAGTCTCGTT | 672 |
rs75371343 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117041 | GAACACTTTACAGAT[A/G]GTACTGTGTACTCTT | 672 |
rs75498718 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049416 | TCAGTCTCCATAAGG[C/T]CACTTGGTATAAGGT | 672 |
rs75562004 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056188 | TCTTTTTTTTTTTTT[C/T]TTCTTTTGAGATCTT | 672 |
rs75604863 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049418 | AGTCTCCATAAGGCC[A/T]CTTGGTATAAGGTTT | 672 |
rs75626303 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074724 | CATATAACATGGGGT[G/T]GGGTTGGTCTGAGGC | 672 |
rs75754723 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083089 | AAATATAAAAATACT[A/G]TCAGTAATCCTGCCT | 672 |
rs75830915 | snp | G/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098835 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTTTCACT | 672 |
rs75854232 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046759 | TGAGACTCCACCTCA[A/C]AAAAAAAAAAAAAAG | 672 |
rs75858602 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101513 | ACAATTACTTTTTTT[C/T]CTTTTTTGAGACAGA | 672 |
rs75947060 | in-del | -/TT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072580 | TGATTTTTTTTTTTT[-/TT]GAGATGGAGTTTCAT | 672 |
rs76215381 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099522 | GTGATCCACCCACTT[C/T]GGCCTCCCAAAGTGC | 672 |
rs76318199 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049419 | GTCTCCATAAGGCCA[C/T]TTGGTATAAGGTTTG | 672 |
rs76331837 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078776 | TTGTTAAGAACTCTG[C/T]TGAAAGTAAGTAGGA | 672 |
rs76381085 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115501 | AGCGAGACTTTGTCT[A/C]AAAAAAAAAAAAAAA | 672 |
rs76400361 | snp | G/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075575 | CTCTCTTTTTTTTTT[G/T]GTTTTGAGACGGAGT | 672 |
rs76558677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046902 | AAAGGAAAGCCACCA[G/T]GAAAACAGCACTGTA | 672 |
rs76700125 | snp | G/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102087 | TTTTTTGTTTTTTTT[G/T]TGAGACAGAGTCTCA | 672 |
rs76731038 | snp | A/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062261 | GCCATGCCCGGCTAA[A/T]TAAAAAAAAATTTTG | 672 |
rs76938847 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103468 | CGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 672 |
rs77008361 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080276 | AGACACTGGAAGACA[A/G]CAGATATTAAGAAAT | 672 |
rs77473713 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081018 | GTTGTGATATCCAAA[A/G]CAATTCAGAAATTAA | 672 |
rs77510730 | snp | A/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048533 | CTTTTTTTTTTTTTT[A/T]AGACAAAGTCTCACT | 672 |
rs77581998 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050608 | ACAGAGACTCGACCT[A/C]AAAAAAAAAGAAAAA | 672 |
rs77583369 | snp | G/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102089 | TTTTGTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 672 |
rs77611824 | snp | A/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108056 | GGGCTAAAAAAAAAG[A/T]CACTAGGGCTGTGCA | 672 |
rs77684117 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090065 | AAAAAAAAAAAGAAG[-/A]AGAGAAAGAAGTATC | 672 |
rs77693534 | snp | A/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111210 | ATTATTATCTTTTTT[A/T]ATAGGCTTCATAAAA | 672 |
rs77997287 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115502 | GCGAGACTTTGTCTC[A/C]AAAAAAAAAAAAAAG | 672 |
rs78201503 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050609 | CAGAGACTCGACCTC[A/C]AAAAAAAAGAAAAAA | 672 |
rs78286195 | snp | A/G | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090060 | AAGGGAAAAAAAAAA[A/G]GAAGAAGAGAAAGAA | 672 |
rs78350562 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126565 | TTTTTCCGTGTCTCC[A/G]GACAGCTAATCGTTT | 672 |
rs78422766 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097619 | AAAAACAAAAAAAAA[A/G]CACAGGCTCTGACAT | 672 |
rs78467612 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049417 | CAGTCTCCATAAGGC[A/C]ACTTGGTATAAGGTT | 672 |
rs78506123 | snp | A/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099288 | TCTCTTTTTTTTTTT[A/T]AGATGGAGTTTCGCT | 672 |
rs78667772 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099289 | CTCTTTTTTTTTTTT[A/G]GATGGAGTTTCGCTA | 672 |
rs78695654 | snp | C/T | 0.031825 | 0.122064 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054080 | TCATTACTTTGACCA[C/T]ATACTTTCCATCATT | 672 |
rs78734003 | snp | A/G | 0.444444 | 0.157135 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090061 | AGGGAAAAAAAAAAA[A/G]AAGAAGAGAAAGAAG | 672 |
rs78735591 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118394 | TTTTCTTTTTTTTTT[C/T]CAGACAGAGTCTCGT | 672 |
rs78800885 | snp | A/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062263 | CATGCCCGGCTAATT[A/T]AAAAAAAATTTTGTG | 672 |
rs78951648 | snp | C/T | 6.32811e-05 | 0.00562464 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43090963 | GTGGTTAAAATGTCA[C/T]TCTGAGAGGATAGCC | 672 |
rs79046304 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087979 | GCAGCCTTGACCTCC[A/G]GGGCTCAGGCAATCT | 672 |
rs79415432 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114335 | TCATCCAGATAAATT[A/G]AAAGCCCCAGGGCTT | 672 |
rs79460193 | snp | G/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084049 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCACT | 672 |
rs79477535 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108054 | AGGGGCTAAAAAAAA[A/G]GTCACTAGGGCTGTG | 672 |
rs79497910 | snp | A/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083189 | CTTTCTTTTTTTTTT[A/T]AAGTCTCCCTCTGTC | 672 |
rs79540890 | snp | G/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045939 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTTG | 672 |
rs79727659 | snp | A/G | 1.64741e-05 | 0.00286998 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094501 | AAGGTAGATCTGAAT[A/G]CTGATCCCCTGTGTG | 672 |
rs79762526 | snp | A/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062110 | ACACTTTTTTTTTTT[A/T]AAGAGACAGGGTCTT | 672 |
rs79775007 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097620 | AAAACAAAAAAAAAG[C/T]ACAGGCTCTGACATC | 672 |
rs79860047 | snp | A/G | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048534 | TTTTTTTTTTTTTTT[A/G]GACAAAGTCTCACTC | 672 |
rs79885857 | snp | G/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102076 | CCCAGCTAAGTTTTT[G/T]TGTTTTTTTTTTGAG | 672 |
rs79944172 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052637 | TCTTGACCTTCCCAT[G/T]GCAATAAAAAGAAAA | 672 |
rs79996471 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087911 | TAATTTTTTTTTTTT[C/T]CCCAGACAGGGGTTG | 672 |
rs80078547 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102359 | TACAGGCGTGAAGCT[C/T]TTTTTTTTTTTTTTT | 672 |
rs80083136 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098526 | ACCACACCCAGCTAA[-/T]TTTTTTTTTTTTTTG | 672 |
rs80187739 | snp | A/C/G | 1.65176e-05 | 0.00287376 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067608 | GTTGTTATGAAAACA[A/C/G]GTATACCAAGAACCT | 672 |
rs80233169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066275 | AGGACAAATGATCTG[C/T]CTCCTCCCTTTTTTG | 672 |
rs80308573 | snp | A/C | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104058 | GCAAGACTCCATCTC[A/C]AAAAAAAAAAAGAAA | 672 |
rs80346747 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43078210 | TGCCTTAGCCTCCCA[A/T]GAAGATGGGATTATA | 672 |
rs80356827 | snp | A/C/T | | | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124055 | AGAAGTACAAAATGT[A/C/T]ATTAATGCTATGCAG | 672 |
rs80356828 | snp | A/C/G | 0.000399281 | 0.0141238 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091505 | CAAGGAATTGGTTTC[A/C/G]GATGATGAAGAAAGA | 672 |
rs80356829 | snp | C/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045738 | GGACAGTGTAGCACT[C/T]TACCAGTGCCAGGAG | 672 |
rs80356830 | snp | G/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091928 | ACATTTGGCTCAGGG[G/T]TACCGAAGAGGGGCC | 672 |
rs80356831 | snp | A/G/T | 1.64749e-05 | 0.00287005 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43091748 | AGAGGAGAATTTATT[A/G/T]TCATTGAAGAATAGC | 672 |
rs80356832 | snp | C/G/T | | | synonymous-codon, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092963 | ACTTGATGCTCAGTA[C/G/T]TTGCAGAATACATTC | 672 |
rs80356833 | snp | A/C/G/T | 0.000181194 | 0.00951651 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline)/C(germline) | 17:43071101 | TTGAAAGTTCCCCAA[A/C/G/T]TGAAAGTTGCAGAAT | 672 |
rs80356834 | snp | A/C/G | 1.64874e-05 | 0.00287113 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43093638 | AGTCAGTAGAAATCT[A/C/G]AGCCCACCTAATTGT | 672 |
rs80356835 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093452 | AAGTAAAAGACATGA[C/T]AGCGATACTTTCCCA | 672 |
rs80356836 | snp | G/T | 4.94197e-05 | 0.00497066 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43094535 | ATGTAATGATAGGCG[G/T]ACTCCCAGCACAGAA | 672 |
rs80356837 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092387 | TATTAATGAAGTAGG[C/T]TCCAGTACTAATGAA | 672 |
rs80356838 | snp | C/G/T | 0.000148409 | 0.00861303 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43093650 | GCTTGAACTAGTAGT[C/G/T]AGTAGAAATCTAAGC | 672 |
rs80356839 | snp | C/T | 6.61452e-05 | 0.0057505 | BRCA1, NBR2 | 17 | allele_origin=T(germline)/C(germline) | 17:43124022 | AATCTTAGAGTGTCC[C/T]ATCTGGTAAGTCAGC | 672 |
rs80356840 | snp | A/G | 0.000131841 | 0.00811808 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43082414 | TCCAGAACAAAGCAC[A/G]TCAGAAAAAGGTGTG | 672 |
rs80356841 | snp | C/G | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045714 | CCAGGAGCTGGACAC[C/G]TACCTGATACCCCAG | 672 |
rs80356842 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071081 | AGTTGCAGAATCTGC[C/T]CAGAGTCCAGCTGCT | 672 |
rs80356843 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092105 | GGGAAGTAGTCATGC[A/G]TCTCAGGTTTGTTCT | 672 |
rs80356844 | snp | A/C | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057073 | AGGTCCAAAGCGAGC[A/C]AGAGAATCCCAGGAC | 672 |
rs80356845 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43097270 | TGATTCTTCTGAAGA[C/T]ACCGTTAATAAGGCA | 672 |
rs80356846 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091457 | AAATAATCAAGAAGA[A/G]CAAAGCATGGATTCA | 672 |
rs80356847 | snp | A/C/G/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104938 | CCTACAAGAAAGTAC[A/C/G/T]AGATTTAGTCAACTT | 672 |
rs80356848 | snp | A/C/T | | | missense, synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092536 | TGTAAGAAAAATCTG[A/C/T]TAGAGGAAAACTTTG | 672 |
rs80356849 | snp | A/C/G | 1.64982e-05 | 0.00287208 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43045732 | TGTAGCACTCTACCA[A/C/G]TGCCAGGAGCTGGAC | 672 |
rs80356850 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071021 | TGCAATGGAAGAAAG[C/T]GTGAGCAGGGAGAAG | 672 |
rs80356851 | snp | A/G | 0.000988093 | 0.0222052 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092717 | TCAGAAAGATAAGCC[A/G]GTTGATAATGCCAAA | 672 |
rs80356852 | snp | G/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091772 | TACCGAGTGTCTGTC[G/T]AAGAACACAGAGGAG | 672 |
rs80356853 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067609 | TGTTGTTATGAAAAC[A/G]GGTATACCAAGAACC | 672 |
rs80356854 | snp | A/G | 1.64727e-05 | 0.00286986 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43057052 | ATCCCAGGACAGAAA[A/G]GTAAAGCTCCCTCCC | 672 |
rs80356855 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091573 | CCTTTCTTGATTGGT[C/T]CTTCCAAACAAATGA | 672 |
rs80356856 | snp | C/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082447 | AAGTGACTCTTCTGC[C/G]CTTGAGGACCTGCGA | 672 |
rs80356857 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090944 | CATTTTAACCACTCA[A/G]GTAAAAAGCGTGTGT | 672 |
rs80356858 | snp | C/G/T | 0.00151286 | 0.0274616 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43063913 | ACACTGAAATATTTT[C/G/T]TAGGAATTGCGGGAG | 672 |
rs80356859 | snp | C/T | 1.6516e-05 | 0.00287362 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093759 | CTATAAGCAGCAGTA[C/T]AAGCAATATGGAACT | 672 |
rs80356860 | snp | A/C/G | 8.28919e-05 | 0.00643732 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43063909 | TGAAATATTTTCTAG[A/C/G]AATTGCGGGAGGAAA | 672 |
rs80356861 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094631 | CAGAATGAATGTAGA[A/C]AAGGCTGAATTCTGT | 672 |
rs80356862 | snp | C/G | 1.6473e-05 | 0.00286988 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43071046 | ATACTACTGATACTG[C/G]TGGGTATAATGCAAT | 672 |
rs80356863 | snp | A/C | 3.58802e-05 | 0.00423543 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43115726 | ACCACATATTTTGCA[A/C]GTAAGTTTGAATGTG | 672 |
rs80356864 | snp | A/C/T | | | missense, stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106508 | CTGAAACTTCTCAAC[A/C/T]AGAAGAAAGGGCCTT | 672 |
rs80356865 | snp | A/T | 1.681e-05 | 0.00289909 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43094797 | AACCCAGTAATAATG[A/T]TTTGAACACCACTGA | 672 |
rs80356866 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091690 | TTGGCAAAGGCATCT[C/T]AGGAACATCACCTTA | 672 |
rs80356867 | snp | G/T | 3.30202e-05 | 0.00406313 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43092164 | CAGACTGTTAATACA[G/T]ATTTCTCTCCATATC | 672 |
rs80356868 | snp | G/T | | | stop-gained, missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047661 | CCAGATGCCTGGACA[G/T]AGGACAATGGCTTCC | 672 |
rs80356869 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093249 | GGGTTTTGCAAACTG[A/C]AAGATCTGTAGAGAG | 672 |
rs80356870 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076518 | CTGCAGATAGTTCTA[C/T]CAGTAAAAATAAAGA | 672 |
rs80356871 | snp | A/C/T | 3.91453e-05 | 0.00442396 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43090998 | TGAGAGTGAAACAAG[A/C/T]GTCTCTGAAGACTGC | 672 |
rs80356872 | snp | A/C/T | | | stop-gained, missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092610 | ATAAACATGGACTTT[A/C/T]ACAAAACCCATATCG | 672 |
rs80356873 | snp | C/T | | | stop-gained, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045734 | AGTGTAGCACTCTAC[C/T]AGTGCCAGGAGCTGG | 672 |
rs80356874 | snp | G/T | 3.29554e-05 | 0.00405914 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43092862 | TCTCTGCCCACTCTG[G/T]GTCCTTAAAGAAACA | 672 |
rs80356875 | snp | A/G/T | 3.29902e-05 | 0.00406128 | BRCA1 | 17 | allele_origin=G(germline)/T(inherited)/A(inherited) | 17:43093373 | ACCAGTGAACTTAAA[A/G/T]AATTTGTCAATCCTA | 672 |
rs80356876 | snp | C/G | 4.94539e-05 | 0.00497238 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43091874 | GAACTTATCTAGTGA[C/G]GATGAAGAGCTTCCC | 672 |
rs80356877 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094605 | TCTGTAATAAAAGCA[A/C]ACAGCCTGGCTTAGC | 672 |
rs80356878 | snp | A/C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092659 | TGTCTATCATCTCAG[A/C/T]TCAGAGGCAACGAAA | 672 |
rs80356879 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067635 | AATCTAATTACTGAA[G/T]AGACTACTCATGTTG | 672 |
rs80356880 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115750 | AGGAACCTGTCTCCA[A/C/G]AAAGTGTGACCACAT | 672 |
rs80356881 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074454 | TGCTCTGGGAGTCTT[C/T]AGAATAGAAACTACC | 672 |
rs80356882 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082556 | GGGATACCATGCAAC[A/G]TAACCTGATAAAGCT | 672 |
rs80356883 | snp | A/T | | | missense, utr-variant-5-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106533 | CTTTATAATTTATAG[A/T]TTTTGCATGCTGAAA | 672 |
rs80356884 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093263 | GTTAAGTGGAGAAAG[C/G]GTTTTGCAAACTGAA | 672 |
rs80356885 | snp | A/G | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074482 | ATTAGATGATAGGTG[A/G]TACATGCACAGTTGC | 672 |
rs80356886 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091520 | AGTTGGTCTGAGTGA[C/G]AAGGAATTGGTTTCA | 672 |
rs80356887 | snp | C/T | 3.30175e-05 | 0.00406296 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092154 | ATACAGATTTCTCTC[C/T]ATATCTGATTTCAGA | 672 |
rs80356888 | snp | A/C/T | 1.64732e-05 | 0.0028699 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43104173 | CCAAAGTATGGGCTA[A/C/T]AGAAACCGTGCCAAA | 672 |
rs80356889 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093532 | CACAGCAGAAACCTA[C/T]AACTCATGGAAGGTA | 672 |
rs80356890 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067629 | ATTACTGAAGAGACT[A/G]CTCATGTTGTTATGA | 672 |
rs80356891 | snp | A/C/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094179 | GAGTTCACTCCAAAT[A/C/G]AGTAGAGAGTAATAT | 672 |
rs80356892 | snp | C/T | 0.00302865 | 0.0387963 | BRCA1 | 17 | allele_origin=T(germline)/C(germline,somatic) | 17:43092965 | GAACTTGATGCTCAG[C/T]ATTTGCAGAATACAT | 672 |
rs80356893 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093919 | AATCAGGGAACTAAC[C/T]AAACGGAGCAGAATG | 672 |
rs80356894 | snp | A/G/T | 0.000307953 | 0.0124049 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43091879 | GAAGAGAACTTATCT[A/G/T]GTGAGGATGAAGAGC | 672 |
rs80356895 | snp | C/T | 6.59217e-05 | 0.00574078 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093525 | GAAACCTACAACTCA[C/T]GGAAGGTAAAGAACC | 672 |
rs80356896 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063946 | CATTCTGCAGATGCT[G/T]AGTTTGTGTGTGAAC | 672 |
rs80356897 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099853 | CTCAGTGTCCAACTC[C/T]CTAACCTTGGAACTG | 672 |
rs80356898 | snp | C/T | 8.26016e-05 | 0.00642604 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093844 | AAAGGTGATTCTATT[C/T]AGAATGAGAAAAATC | 672 |
rs80356899 | snp | A/G/T | 4.94328e-05 | 0.00497131 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43092388 | ATATTAATGAAGTAG[A/G/T]TTCCAGTACTAATGA | 672 |
rs80356900 | snp | A/G | 3.30011e-05 | 0.00406195 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092226 | GTCTTCCTGGAAGTA[A/G]TTGTAAGCATCCTGA | 672 |
rs80356901 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092268 | TGCTTAGATTAGGGG[A/T]TTTGCAACCTGAGGT | 672 |
rs80356902 | snp | A/C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093634 | AGTAGAAATCTAAGC[A/C/T]CACCTAATTGTACTG | 672 |
rs80356903 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091813 | AACAATATACCTTCT[C/T]AGTCTACTAGGCATA | 672 |
rs80356904 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093910 | ACTAACCAAACGGAG[C/T]AGAATGGTCAAGTGA | 672 |
rs80356905 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051113 | TCTTCTTCCAGATCT[C/T]CAGGGGGCTAGAAAT | 672 |
rs80356906 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074337 | TACTTGCCAAGGCAA[C/G]ATCTAGGTAATATTT | 672 |
rs80356907 | snp | C/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093586 | TGTTCTAGCAGTGAA[C/G/T]AGATAAAGAAAAAAA | 672 |
rs80356908 | snp | A/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094473 | GTGAGAGAAAAGAAT[A/G]GAATAAGCAGAAACT | 672 |
rs80356909 | snp | C/T | 4.95503e-05 | 0.00497722 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43071185 | TCTGATGACCCTGAA[C/T]CTGATCCTTCTGAAG | 672 |
rs80356910 | snp | C/G/T | 3.30349e-05 | 0.00406403 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43093828 | AGAATGAGAAAAATC[C/G/T]TAACCCAATAGAATC | 672 |
rs80356911 | snp | A/G | 6.5937e-05 | 0.00574144 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092934 | TCAAGGTTTCAAAGC[A/G]CCAGTCATTTGCTCC | 672 |
rs80356912 | snp | C/T | 3.29984e-05 | 0.00406179 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093351 | TCAATCCTAGCCTTC[C/T]AAGAGAAGAAAAAGA | 672 |
rs80356913 | snp | A/G/T | | | missense, intron-variant | BRCA1 | GRCh38.p7 | 17:43106456 | ATGATATAACCAAAA[A/G/T]GTATATAATTTGGTA | 672 |
rs80356914 | snp | A/G/T | | | stop-gained, missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045759 | GGTGACCCGAGAGTG[A/G/T]GTGTTGGACAGTGTA | 672 |
rs80356915 | snp | C/G/T | 8.2445e-05 | 0.00641995 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43094198 | TTAATATGTAAAAGT[C/G/T]AAAGAGTTCACTCCA | 672 |
rs80356916 | snp | C/G/T | 1.64798e-05 | 0.00287047 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43082550 | CCATGCAACATAACC[C/G/T]GATAAAGCTCCAGCA | 672 |
rs80356917 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074375 | TGGAAGAGTCTGGGC[C/T]ACACGATTTGACGGA | 672 |
rs80356918 | snp | C/T | 0.000399281 | 0.0141238 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092043 | AAATAAAGGAAGATA[C/T]TAGTTTTGCTGAAAA | 672 |
rs80356919 | snp | A/G | 3.30202e-05 | 0.00406313 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092169 | TAGTTCAGACTGTTA[A/G]TACAGATTTCTCTCC | 672 |
rs80356920 | snp | A/T | 0.000115353 | 0.00759362 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43047699 | TGGGGATCCAGGGTG[A/T]CCACCCAATTGTGGT | 672 |
rs80356921 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091876 | GAGAACTTATCTAGT[A/G]AGGATGAAGAGCTTC | 672 |
rs80356922 | snp | A/G/T | | | synonymous-codon, missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092099 | TAGTCATGCATCTCA[A/G/T]GTTTGTTCTGAGACA | 672 |
rs80356923 | snp | A/G/T | 0.000164992 | 0.00908123 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43091891 | TTAGAGTCCTCAGAA[A/G/T]AGAACTTATCTAGTG | 672 |
rs80356924 | snp | A/T | 1.64792e-05 | 0.00287042 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43094641 | TCACTAAAGACAGAA[A/T]GAATGTAGAAAAGGC | 672 |
rs80356925 | snp | A/C/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092928 | TTTCAAAGCGCCAGT[A/C/G]ATTTGCTCCGTTTTC | 672 |
rs80356926 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070981 | ACAGCTTCAACAGAA[A/G]GGGTCAACAAAAGAA | 672 |
rs80356927 | snp | A/G | 0.000197791 | 0.00994266 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092947 | TTGCAGAATACATTC[A/G]AGGTTTCAAAGCGCC | 672 |
rs80356928 | snp | A/G/T | 4.9525e-05 | 0.00497595 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43093784 | TCTGCTTTCAAAACG[A/G/T]AAGCTGAACCTATAA | 672 |
rs80356929 | snp | A/C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124044 | ATGTCATTAATGCTA[A/C/T]GCAGAAAATCTTAGA | 672 |
rs80356930 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071181 | ATGACCCTGAATCTG[A/G]TCCTTCTGAAGACAG | 672 |
rs80356932 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076600 | GCAGTATTAACTTCA[C/T]AGAAAAGTAGTGAAT | 672 |
rs80356933 | snp | A/G/T | 3.29875e-05 | 0.00406112 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43092491 | TCACCTGAAAGAGAA[A/G/T]TGGGAAATGAGAACA | 672 |
rs80356934 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094323 | CACATGATGGGGAGT[C/T]TGAATCAAATGCCAA | 672 |
rs80356935 | snp | A/C/G | | | stop-gained, missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094472 | TGAGAGAAAAGAATG[A/C/G]AATAAGCAGAAACTG | 672 |
rs80356936 | snp | C/G/T | 1.65567e-05 | 0.00287716 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43104260 | CTTGTATTTTACAGA[C/G/T]GCAAACAGCTATAAT | 672 |
rs80356937 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057117 | GATTTTGAAGTCAGA[A/G]GAGATGTGGTCAATG | 672 |
rs80356938 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070962 | TCAACAAAAGAATGT[C/T]CATGGTGGTGTCTGG | 672 |
rs80356939 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093798 | CACTCGAAAAAGAAT[A/C]TGCTTTCAAAACGAA | 672 |
rs80356941 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092733 | GCTTTCCTGTGGTTG[A/C/G]TCAGAAAGATAAGCC | 672 |
rs80356942 | snp | A/G/T | 1.648e-05 | 0.0028705 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43045764 | CCTGTGGTGACCCGA[A/G/T]AGTGGGTGTTGGACA | 672 |
rs80356943 | snp | A/G | 3.29468e-05 | 0.00405861 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43071098 | AAAGTTCCCCAATTG[A/G]AAGTTGCAGAATCTG | 672 |
rs80356944 | snp | A/C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091944 | GCCCTTTCACCCATA[A/C/T]ACATTTGGCTCAGGG | 672 |
rs80356945 | snp | A/C/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093193 | ACTGATTATGGCACT[A/C/G/T]AGGAAAGTATCTCGT | 672 |
rs80356946 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094450 | CAGAAACTGCCATGC[C/T]CAGAGAATCCTAGAG | 672 |
rs80356947 | snp | C/T | 1.64732e-05 | 0.0028699 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43099808 | ACAAAGCAGCGGATA[C/T]AACCTCAAAAGACGT | 672 |
rs80356948 | snp | A/G | 0.00016478 | 0.0090754 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093184 | GGCACTCAGGAAAGT[A/G]TCTCGTTACTGGAAG | 672 |
rs80356949 | snp | A/T | 1.65097e-05 | 0.00287308 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43092176 | GAAGAAGTAGTTCAG[A/T]CTGTTAATACAGATT | 672 |
rs80356950 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093661 | CATATTCATGCGCTT[A/G/T]AACTAGTAGTCAGTA | 672 |
rs80356951 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092986 | AGCATAGAAATGGAA[G/T]AAAGTGAACTTGATG | 672 |
rs80356952 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093901 | ACGGAGCAGAATGGT[C/T]AAGTGATGAATATTA | 672 |
rs80356953 | snp | A/C/G | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074519 | TTTATCTTTCTAGGT[A/C/G]ATCCCCTTCTAAATG | 672 |
rs80356954 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091591 | AATACAAACACCCAG[A/G]ATCCTTTCTTGATTG | 672 |
rs80356955 | snp | A/G | 1.64874e-05 | 0.00287113 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092647 | CAGTTCAGAGGCAAC[A/G]AAACTGGACTCATTA | 672 |
rs80356956 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106479 | TTCACAGTGTCCTTT[A/T]TGTAAGAATGATATA | 672 |
rs80356957 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057129 | TTCTTTCAGCATGAT[C/T]TTGAAGTCAGAGGAG | 672 |
rs80356958 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067638 | ACTAATCTAATTACT[A/G]AAGAGACTACTCATG | 672 |
rs80356959 | snp | C/G/T | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045761 | GTGGTGACCCGAGAG[C/G/T]GGGTGTTGGACAGTG | 672 |
rs80356960 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076567 | CCTATAAGCCAGAAT[C/T]CAGAAGGCCTTTCTG | 672 |
rs80356961 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094498 | GTAGATCTGAATGCT[G/T]ATCCCCTGTGTGAGA | 672 |
rs80356962 | snp | A/G | | | stop-gained, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047666 | TGCAGCCAGATGCCT[A/G]GACAGAGGACAATGG | 672 |
rs80356963 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104902 | AGAGCTATTGAAAAT[C/G]ATTTGTGCTTTTCAG | 672 |
rs80356964 | snp | C/G/T | 3.29549e-05 | 0.00405911 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43094135 | TTTGGGAAAACCTAT[C/G/T]GGAAGAAGGCAAGCC | 672 |
rs80356967 | snp | A/C/G | 1.64947e-05 | 0.00287177 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43104953 | ATTTAATTTCAGGAG[A/C/G]CTACAAGAAAGTACG | 672 |
rs80356968 | snp | A/C/T | 3.29468e-05 | 0.00405861 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43070959 | ACAAAAGAATGTCCA[A/C/T]GGTGGTGTCTGGCCT | 672 |
rs80356969 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049174 | CTGGAATGGATGGTA[C/T]AGCTGTGTGGTGCTT | 672 |
rs80356970 | snp | A/C/T | 4.95544e-05 | 0.00497742 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43092596 | TTACAAAACCCATAT[A/C/T]GTATACCACCACTTT | 672 |
rs80356971 | snp | A/C/G/T | | | stop-gained, missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092133 | TGATTTCAGATAACT[A/C/G/T]AGAACAGCCTATGGG | 672 |
rs80356972 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090945 | ACATTTTAACCACTC[A/G]GGTAAAAAGCGTGTG | 672 |
rs80356973 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092662 | TTTTGTCTATCATCT[C/T]AGTTCAGAGGCAACG | 672 |
rs80356974 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063917 | ACGGACACTGAAATA[G/T]TTTCTAGGAATTGCG | 672 |
rs80356975 | snp | A/G | 4.97475e-05 | 0.00498711 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091971 | AGAAAGGAGAGCTTA[A/G]CAGGAGTCCTAGCCC | 672 |
rs80356976 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094404 | CTTGGATAACACTAA[A/G]TAGCAGCATTCAGAA | 672 |
rs80356977 | snp | A/C | | | stop-gained, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045735 | CAGTGTAGCACTCTA[A/C]CAGTGCCAGGAGCTG | 672 |
rs80356978 | snp | G/T | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43092809 | TGTGAACAAAAGGAA[G/T]AAAATCAAGGAAAGA | 672 |
rs80356980 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093855 | AGAATAAAACAAAAG[G/T]TGATTCTATTCAGAA | 672 |
rs80356981 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093889 | GGTCAAGTGATGAAT[A/G]TTACTAATAGTGGTC | 672 |
rs80356982 | snp | C/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093121 | AATAAATGTGTGAGT[C/G/T]AGTGTGCAGCATTTG | 672 |
rs80356983 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093636 | TCAGTAGAAATCTAA[A/G]CCCACCTAATTGTAC | 672 |
rs80356984 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093955 | GCAGATTTGGCAGTT[C/T]AAAAGACTCCTGAAA | 672 |
rs80356985 | snp | A/G | 1.65214e-05 | 0.0028741 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092595 | TACAAAACCCATATC[A/G]TATACCACCACTTTT | 672 |
rs80356986 | snp | C/G | 3.92072e-05 | 0.00442742 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43091002 | GGTGTGAGAGTGAAA[C/G]AAGCGTCTCTGAAGA | 672 |
rs80356987 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071071 | TCTGCCCAGAGTCCA[A/G]CTGCTGCTCATACTA | 672 |
rs80356988 | snp | A/C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074331 | CCAAGGCAAGATCTA[A/C/G]GTAATATTTCATCTG | 672 |
rs80356989 | snp | C/T | 1.64776e-05 | 0.00287028 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43082539 | AACCTGATAAAGCTC[C/T]AGCAGGAAATGGCTG | 672 |
rs80356990 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094824 | CGGATGTAACAAATA[C/G]TGAACATCATCAACC | 672 |
rs80356991 | snp | A/G/T | 0.00019769 | 0.00994012 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43104136 | CTACAGAGTGAACCC[A/G/T]AAAATCCTTCCTTGG | 672 |
rs80356992 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074394 | GATGTGGAGGAGCAA[C/T]AGCTGGAAGAGTCTG | 672 |
rs80356993 | snp | A/C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063937 | GATGCTGAGTTTGTG[A/C/T]GTGAACGGACACTGA | 672 |
rs80356994 | snp | A/C/T | 6.63057e-05 | 0.00575752 | BRCA1, NBR2 | 17 | allele_origin=T(germline)/C(germline) | 17:43124078 | GATTTATCTGCTCTT[A/C/T]GCGTTGAAGAAGTAC | 672 |
rs80356995 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092749 | GTTAATATCACTGCA[A/G]GCTTTCCTGTGGTTG | 672 |
rs80356996 | snp | C/T | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045709 | AGCTGGACACCTACC[C/T]GATACCCCAGATCCC | 672 |
rs80356997 | snp | A/C/G/T | 1.64779e-05 | 0.00287031 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43076583 | GAAAAGTAGTGAATA[A/C/G/T]CCTATAAGCCAGAAT | 672 |
rs80356999 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093256 | GGAGAAAGGGTTTTG[C/T]AAACTGAAAGATCTG | 672 |
rs80357000 | snp | C/G | 1.77865e-05 | 0.0029821 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43115767 | TAGTCTGGAGTTGAT[C/G]AAGGAACCTGTCTCC | 672 |
rs80357001 | snp | C/T | 0.00016132 | 0.00897963 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094839 | GTGAATTTTCTGAGA[C/T]GGATGTAACAAATAC | 672 |
rs80357002 | snp | C/T | 3.2963e-05 | 0.00405961 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43071149 | GCCCCAGAGTCAGCT[C/T]GTGTTGGCAACATAC | 672 |
rs80357003 | snp | C/G/T | 1.64841e-05 | 0.00287085 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43092940 | ATACATTCAAGGTTT[C/G/T]AAAGCGCCAGTCATT | 672 |
rs80357004 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092482 | AGAGAAATGGGAAAT[G/T]AGAACATTCCAAGTA | 672 |
rs80357005 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093619 | CCACCTAATTGTACT[A/G/T]AATTGCAAATTGATA | 672 |
rs80357006 | snp | A/C/G/T | 6.59294e-05 | 0.00574111 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline)/C(germline) | 17:43092274 | ATGCTATGCTTAGAT[A/C/G/T]AGGGGTTTTGCAACC | 672 |
rs80357007 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051107 | TCCAGATCTTCAGGG[G/T]GCTAGAAATCTGTTG | 672 |
rs80357008 | snp | C/T | 1.64776e-05 | 0.00287028 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092772 | CTAATATCAAGCCTG[C/T]ACAGACAGTTAATAT | 672 |
rs80357009 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094768 | GAGAAGCGTGCAGCT[G/T]AGAGGCATCCAGAAA | 672 |
rs80357010 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094051 | GAGCCACAGATAATA[C/T]AAGAGCGTCCCCTCA | 672 |
rs80357011 | snp | A/C/T | | | missense, stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082575 | TTATCGTTTTTGAAG[A/C/T]AGAGGGATACCATGC | 672 |
rs80357012 | snp | A/C | 4.95217e-05 | 0.00497578 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43049180 | GATCAACTGGAATGG[A/C]TGGTACAGCTGTGTG | 672 |
rs80357013 | snp | C/T | 3.29495e-05 | 0.00405877 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43082500 | GCTGTGTTAGAACAG[C/T]ATGGGAGCCAGCCTT | 672 |
rs80357015 | snp | C/T | 0.00042823 | 0.0146264 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094495 | GATCTGAATGCTGAT[C/T]CCCTGTGTGAGAGAA | 672 |
rs80357016 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070983 | TGACAGCTTCAACAG[A/G]AAGGGTCAACAAAAG | 672 |
rs80357017 | snp | C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124065 | TTCGCGTTGAAGAAG[C/T]ACAAAATGTCATTAA | 672 |
rs80357018 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092131 | ATTTCAGATAACTTA[G/T]AACAGCCTATGGGAA | 672 |
rs80357019 | snp | C/G | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045743 | GTGTTGGACAGTGTA[C/G]CACTCTACCAGTGCC | 672 |
rs80357020 | snp | A/C/T | 9.89495e-05 | 0.00703313 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43092490 | CACCTGAAAGAGAAA[A/C/T]GGGAAATGAGAACAT | 672 |
rs80357021 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091516 | GGTCTGAGTGACAAG[A/G/T]AATTGGTTTCAGATG | 672 |
rs80357022 | snp | A/C/G | 8.23844e-05 | 0.00641765 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43076570 | TACCCTATAAGCCAG[A/C/G]ATCCAGAAGGCCTTT | 672 |
rs80357023 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057107 | TCAGAGGAGATGTGG[G/T]CAATGGAAGAAACCA | 672 |
rs80357024 | snp | G/T | 8.24872e-05 | 0.00642159 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43094298 | TGCCAAAGTAGCTGA[G/T]GTATTGGACGTTCTA | 672 |
rs80357025 | snp | C/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051083 | TCTGTTGCTATGGGC[C/G/T]CTTCACCAACATGCC | 672 |
rs80357027 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092004 | AGGAAAGTTCTGCTG[A/T]TTTTAGCAAAAGCGT | 672 |
rs80357028 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057074 | AAGGTCCAAAGCGAG[C/T]AAGAGAATCCCAGGA | 672 |
rs80357029 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093523 | AACCTACAACTCATG[A/G]AAGGTAAAGAACCTG | 672 |
rs80357031 | snp | A/C | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124054 | GAAGTACAAAATGTC[A/C]TTAATGCTATGCAGA | 672 |
rs80357032 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091989 | TTTTTAGCAAAAGCG[C/T]CCAGAAAGGAGAGCT | 672 |
rs80357033 | snp | G/T | | | missense, intron-variant | BRCA1 | GRCh38.p7 | 17:43106467 | TTTATGTAAGAATGA[G/T]ATAACCAAAAGGTAT | 672 |
rs80357034 | snp | A/C/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067610 | ATGTTGTTATGAAAA[A/C/G/T]AGGTATACCAAGAAC | 672 |
rs80357035 | snp | C/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092821 | GTCACTTTTGAATGT[C/G/T]AACAAAAGGAAGAAA | 672 |
rs80357036 | snp | A/G | 1.64751e-05 | 0.00287007 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091696 | GTAATATTGGCAAAG[A/G]CATCTCAGGAACATC | 672 |
rs80357037 | snp | A/G | 1.64754e-05 | 0.00287009 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091807 | ATACCTTCTCAGTCT[A/G]CTAGGCATAGCACCG | 672 |
rs80357038 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091636 | AGCTTGTTTTCTTCA[C/T]AGTGCAGTGAATTGG | 672 |
rs80357039 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094680 | ATGCCAGCTCATTAC[A/G]GCATGAGAACAGCAG | 672 |
rs80357040 | snp | A/G | | | missense, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047678 | CAATTGTGGTTGTGC[A/G]GCCAGATGCCTGGAC | 672 |
rs80357041 | snp | A/G | 1.65296e-05 | 0.00287481 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43049194 | AAATGTCCATTTTAG[A/G]TCAACTGGAATGGAT | 672 |
rs80357042 | snp | A/C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091566 | TGATTGGTTCTTCCA[A/C/T]ACAAATGAGGCATCA | 672 |
rs80357043 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067628 | TTACTGAAGAGACTA[C/T]TCATGTTGTTATGAA | 672 |
rs80357045 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099852 | TCAGTGTCCAACTCT[C/G]TAACCTTGGAACTGT | 672 |
rs80357046 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094270 | CTAAATGAGGTAGAT[A/G]AATATTCTGGTTCTT | 672 |
rs80357047 | snp | A/G | 3.29489e-05 | 0.00405874 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091683 | AGGCATCTCAGGAAC[A/G]TCACCTTAGTGAGGA | 672 |
rs80357048 | snp | C/T | 4.94173e-05 | 0.00497053 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43071004 | TGAGCAGGGAGAAGC[C/T]AGAATTGACAGCTTC | 672 |
rs80357049 | snp | C/T | 4.94401e-05 | 0.00497168 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092449 | GTGAGCACAATTAGC[C/T]GTAATAACATTAGAG | 672 |
rs80357050 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094588 | CAGCCTGGCTTAGCA[A/G]GGAGCCAACATAACA | 672 |
rs80357051 | snp | C/G/T | 1.64811e-05 | 0.00287059 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43093309 | AAACAGTTAAAGTGT[C/G/T]TAATAATGCTGAAGA | 672 |
rs80357052 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071190 | TCTTCTCTGATGACC[A/C]TGAATCTGATCCTTC | 672 |
rs80357055 | snp | A/C | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049140 | TGGTGAAGGAGCTTT[A/C]ATCATTCACCCTTGG | 672 |
rs80357056 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093631 | AGAAATCTAAGCCCA[C/T]CTAATTGTACTGAAT | 672 |
rs80357057 | snp | A/G/T | 4.94249e-05 | 0.00497096 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43094113 | AGGCAAGCCTCCCCA[A/G/T]CTTAAGCCATGTAAC | 672 |
rs80357058 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093343 | AGCCTTCCAAGAGAA[G/T]AAAAAGAAGAGAAAC | 672 |
rs80357060 | snp | A/G | 1.6483e-05 | 0.00287076 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093169 | ATCTCGTTACTGGAA[A/G]TTAGCACTCTAGGGA | 672 |
rs80357061 | snp | C/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067616 | CTACTCATGTTGTTA[C/G/T]GAAAACAGGTATACC | 672 |
rs80357062 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094788 | ATAATGATTTGAACA[A/C]CACTGAGAAGCGTGC | 672 |
rs80357063 | snp | A/C/T | | | stop-gained, missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093222 | AGAGTAGCAGTATTT[A/C/T]ATTGGTACCTGGTAC | 672 |
rs80357064 | snp | C/G/T | 3.36632e-05 | 0.0041025 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43106478 | TCACAGTGTCCTTTA[C/G/T]GTAAGAATGATATAA | 672 |
rs80357065 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049168 | TGGATGGTACAGCTG[A/T]GTGGTGCTTCTGTGG | 672 |
rs80357066 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115763 | CTGGAGTTGATCAAG[C/G]AACCTGTCTCCACAA | 672 |
rs80357067 | snp | A/C/T | | | missense, stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082422 | CTGCGAAATCCAGAA[A/C/T]AAAGCACATCAGAAA | 672 |
rs80357068 | snp | A/C/G/T | 1.64904e-05 | 0.00287139 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43094338 | TAGGTTCTGATGACT[A/C/G/T]ACATGATGGGGAGTC | 672 |
rs80357069 | snp | A/G/T | 3.29947e-05 | 0.00406159 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43049164 | TGGTACAGCTGTGTG[A/G/T]TGCTTCTGTGGTGAA | 672 |
rs80357070 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071164 | CCTTCTGAAGACAGA[G/T]CCCCAGAGTCAGCTC | 672 |
rs80357071 | snp | C/G | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090981 | TCTCTGAAGACTGCT[C/G]AGGGCTATCCTCTCA | 672 |
rs80357072 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071091 | CCCAATTGAAAGTTG[C/T]AGAATCTGCCCAGAG | 672 |
rs80357073 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094125 | CCTATCGGAAGAAGG[C/G]AAGCCTCCCCAACTT | 672 |
rs80357074 | snp | A/C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057075 | CAAGGTCCAAAGCGA[A/C/G]CAAGAGAATCCCAGG | 672 |
rs80357075 | snp | A/T | 4.94287e-05 | 0.00497111 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43076562 | AAGCCAGAATCCAGA[A/T]GGCCTTTCTGCTGAC | 672 |
rs80357076 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074357 | ACGATTTGACGGAAA[C/T]ATCTTACTTGCCAAG | 672 |
rs80357077 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092713 | AAAGATAAGCCAGTT[G/T]ATAATGCCAAATGTA | 672 |
rs80357078 | snp | A/G/T | 1.64963e-05 | 0.00287192 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43049162 | GTACAGCTGTGTGGT[A/G/T]CTTCTGTGGTGAAGG | 672 |
rs80357079 | snp | A/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082499 | CTGTGTTAGAACAGC[A/G/T]TGGGAGCCAGCCTTC | 672 |
rs80357080 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092614 | CCAAATAAACATGGA[C/G]TTTTACAAAACCCAT | 672 |
rs80357081 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095879 | ACCCCTCAAGGAACC[A/G]GGGATGAAATCAGTT | 672 |
rs80357082 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093496 | CCTGCAACTGGAGCC[A/T]AGAAGAGTAACAAGC | 672 |
rs80357083 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094279 | TTGGACGTTCTAAAT[G/T]AGGTAGATGAATATT | 672 |