SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs80357084 | snp | A/C/T | 0.000254403 | 0.0112755 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43106514 | TGCATGCTGAAACTT[A/C/T]TCAACCAGAAGAAAG | 672 |
rs80357085 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093237 | CTGAAAGATCTGTAG[A/G]GAGTAGCAGTATTTC | 672 |
rs80357086 | snp | A/C/T | 1.6825e-05 | 0.00290038 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43106480 | CTTCACAGTGTCCTT[A/C/T]ATGTAAGAATGATAT | 672 |
rs80357087 | snp | A/G/T | 0.000115454 | 0.00759704 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43067677 | CTCGTGTACAAGTTT[A/G/T]CCAGAAAACACCACA | 672 |
rs80357088 | snp | G/T | 1.76459e-05 | 0.00297029 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43095855 | ATCAGTTTGGATTCT[G/T]CAAAAAAGGGTAATG | 672 |
rs80357089 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092200 | CCTGAAATAAAAAAG[C/T]AAGAATATGAAGAAG | 672 |
rs80357090 | snp | A/G | 0.000594383 | 0.017229 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43097266 | TCTTCTGAAGATACC[A/G]TTAATAAGGCAACTT | 672 |
rs80357091 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104910 | CTTGTTGAAGAGCTA[G/T]TGAAAATCATTTGTG | 672 |
rs80357093 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106486 | AAGGGCCTTCACAGT[A/G]TCCTTTATGTAAGAA | 672 |
rs80357094 | snp | A/C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063881 | AAAATGGGTAGTTAG[A/C/G]TATTTCTGTAAGTAT | 672 |
rs80357095 | snp | A/G | 1.64754e-05 | 0.00287009 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43074421 | TCTCAAGAGGAGCTC[A/G]TTAAGGTTGTTGATG | 672 |
rs80357096 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071229 | TTTCAGAGGGAACCC[C/T]TTACCTGGAATCTGG | 672 |
rs80357097 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104903 | AAGAGCTATTGAAAA[C/T]CATTTGTGCTTTTCA | 672 |
rs80357098 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092949 | ATTTGCAGAATACAT[G/T]CAAGGTTTCAAAGCG | 672 |
rs80357099 | snp | C/G | 3.29506e-05 | 0.00405884 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43091785 | ATAGCACCGTTGCTA[C/G]CGAGTGTCTGTCTAA | 672 |
rs80357101 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092107 | ATGGGAAGTAGTCAT[C/G]CATCTCAGGTTTGTT | 672 |
rs80357102 | snp | A/G/T | 0.000152378 | 0.00872731 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43106469 | CCTTTATGTAAGAAT[A/G/T]ATATAACCAAAAGGT | 672 |
rs80357103 | snp | A/G | 1.64789e-05 | 0.0028704 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094640 | CACTAAAGACAGAAT[A/G]AATGTAGAAAAGGCT | 672 |
rs80357104 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063361 | TAGGGGTGACCCAGT[C/T]TATTAAAGAAAGAAA | 672 |
rs80357105 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093604 | GAATTGCAAATTGAT[A/G]GTTGTTCTAGCAGTG | 672 |
rs80357106 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092212 | AATTGTAAGCATCCT[G/T]AAATAAAAAAGCAAG | 672 |
rs80357107 | snp | A/T | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045757 | TGACCCGAGAGTGGG[A/T]GTTGGACAGTGTAGC | 672 |
rs80357108 | snp | A/G | 1.64803e-05 | 0.00287052 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093084 | CCAAGGGACTAATTC[A/G]TGGTTGTTCCAAAGA | 672 |
rs80357109 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095915 | CCCTATAGTGTGGGA[A/G]ATCAAGAATTGTTAC | 672 |
rs80357110 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104883 | TGTGCTTTTCAGCTT[A/G]ACACAGGTTTGGAGT | 672 |
rs80357111 | snp | C/G/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124095 | TGGAACAGAAAGAAA[C/G/T]GGATTTATCTGCTCT | 672 |
rs80357112 | snp | A/C/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051063 | ACCAACATGCCCACA[A/C/G/T]GTAAGAGCCTGGGAG | 672 |
rs80357113 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094281 | TATTGGACGTTCTAA[A/G]TGAGGTAGATGAATA | 672 |
rs80357114 | snp | A/C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093286 | GCTGAAGACCCCAAA[A/C/G/T]ATCTCATGTTAAGTG | 672 |
rs80357115 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092597 | TTTACAAAACCCATA[G/T]CGTATACCACCACTT | 672 |
rs80357116 | snp | A/G/T | | | missense, intron-variant | BRCA1 | GRCh38.p7 | 17:43106465 | TATGTAAGAATGATA[A/G/T]AACCAAAAGGTATAT | 672 |
rs80357117 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067695 | TTGATTTAATTTCAG[A/T]TGCTCGTGTACAAGT | 672 |
rs80357118 | snp | A/G/T | 3.30371e-05 | 0.00406417 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43093738 | ATATGGAACTCGAAT[A/G/T]AAATATCCACAATTC | 672 |
rs80357119 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071212 | TACCTGGAATCTGGA[A/G]TCAGCCTCTTCTCTG | 672 |
rs80357120 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092881 | GAAGAGGAATGTGCA[A/G]CATTCTCTGCCCACT | 672 |
rs80357121 | snp | C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093630 | GAAATCTAAGCCCAC[C/G/T]TAATTGTACTGAATT | 672 |
rs80357122 | snp | A/G | 9.92884e-05 | 0.00704517 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093970 | GATTTTATCAAGAAA[A/G]CAGATTTGGCAGTTC | 672 |
rs80357123 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057078 | CACCAAGGTCCAAAG[C/T]GAGCAAGAGAATCCC | 672 |
rs80357124 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092533 | AAGAAAAATCTGCTA[A/G]AGGAAAACTTTGAGG | 672 |
rs80357125 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063940 | GCAGATGCTGAGTTT[C/G]TGTGTGAACGGACAC | 672 |
rs80357126 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076512 | ATAGTTCTACCAGTA[A/G]AAATAAAGAACCAGG | 672 |
rs80357127 | snp | A/T | 9.88728e-05 | 0.00703041 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43092805 | AACAAAAGGAAGAAA[A/T]TCAAGGAAAGAATGA | 672 |
rs80357129 | snp | A/C | 4.94564e-05 | 0.0049725 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43093597 | AAATTGATAGTTGTT[A/C]TAGCAGTGAAGAGAT | 672 |
rs80357130 | snp | C/G | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076602 | AAGCAGTATTAACTT[C/G]ACAGAAAAGTAGTGA | 672 |
rs80357131 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092968 | AGTGAACTTGATGCT[C/T]AGTATTTGCAGAATA | 672 |
rs80357132 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063888 | CGGGAGGAAAATGGG[C/T]AGTTAGCTATTTCTG | 672 |
rs80357133 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099817 | ACTCTGAGGACAAAG[C/T]AGCGGATACAACCTC | 672 |
rs80357134 | snp | C/T | 1.65291e-05 | 0.00287476 | BRCA1, NBR2 | 17 | allele_origin=T(germline)/C(germline) | 17:43124063 | CGCGTTGAAGAAGTA[C/T]AAAATGTCATTAATG | 672 |
rs80357135 | snp | A/G/T | 1.6504e-05 | 0.00287258 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43092223 | TTCCTGGAAGTAATT[A/G/T]TAAGCATCCTGAAAT | 672 |
rs80357136 | snp | C/G/T | 4.95089e-05 | 0.00497518 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092128 | TCAGATAACTTAGAA[C/G/T]AGCCTATGGGAAGTA | 672 |
rs80357137 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074472 | AGGTGGTACATGCAC[A/T]GTTGCTCTGGGAGTC | 672 |
rs80357138 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094776 | ACACCACTGAGAAGC[A/G]TGCAGCTGAGAGGCA | 672 |
rs80357139 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094429 | AATCCTAGAGATACT[G/T]AAGATGTTCCTTGGA | 672 |
rs80357140 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094538 | AACATGTAATGATAG[C/G]CGGACTCCCAGCACA | 672 |
rs80357141 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091833 | ACTTGTTATTTGGTA[A/G]AGTAAACAATATACC | 672 |
rs80357142 | snp | A/T | 1.65135e-05 | 0.00287341 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43097265 | CTTCTGAAGATACCG[A/T]TAATAAGGCAACTTA | 672 |
rs80357143 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091809 | ATATACCTTCTCAGT[A/C/G]TACTAGGCATAGCAC | 672 |
rs80357144 | snp | A/G | 1.64819e-05 | 0.00287066 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093115 | TGTGTGAGTCAGTGT[A/G]CAGCATTTGAAAACC | 672 |
rs80357145 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092292 | ACAGAGGGCCAAAAT[A/T]GAATGCTATGCTTAG | 672 |
rs80357146 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057093 | GTCAATGGAAGAAAC[A/C]ACCAAGGTCCAAAGC | 672 |
rs80357147 | snp | A/G/T | 8.24749e-05 | 0.00642111 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43093376 | AATACCAGTGAACTT[A/G/T]AAGAATTTGTCAATC | 672 |
rs80357148 | snp | A/G/T | 1.64787e-05 | 0.00287038 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43076492 | AAAGAACCAGGAGTG[A/G/T]AAAGGTAAGAAACAT | 672 |
rs80357149 | snp | C/G | | | missense, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047702 | TCCTGGGGATCCAGG[C/G]TGTCCACCCAATTGT | 672 |
rs80357150 | snp | A/G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106528 | TAATTTATAGATTTT[A/G/T]CATGCTGAAACTTCT | 672 |
rs80357151 | snp | C/G | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074350 | GACGGAAACATCTTA[C/G]TTGCCAAGGCAAGAT | 672 |
rs80357152 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091909 | CGAAGAGGGGCCAAG[A/G]AATTAGAGTCCTCAG | 672 |
rs80357153 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093775 | AAAACGAAAGCTGAA[C/T]CTATAAGCAGCAGTA | 672 |
rs80357154 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092485 | GAAAGAGAAATGGGA[A/G]ATGAGAACATTCCAA | 672 |
rs80357157 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082467 | AACAGCTACCCTTCC[A/C]TCATAAGTGACTCTT | 672 |
rs80357158 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071030 | TGGGTATAATGCAAT[G/T]GAAGAAAGTGTGAGC | 672 |
rs80357159 | snp | C/T | 3.3024e-05 | 0.00406336 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093819 | AAAATCCTAACCCAA[C/T]AGAATCACTCGAAAA | 672 |
rs80357160 | snp | C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091734 | TATCATTGAAGAATA[C/G/T]CTTAAATGACTGCAG | 672 |
rs80357161 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092419 | GAAAATGTTTTTAAA[G/T]AAGCCAGCTCAAGCA | 672 |
rs80357162 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091842 | GCTTCCAACACTTGT[G/T]ATTTGGTAAAGTAAA | 672 |
rs80357163 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115736 | ACAAAGTGTGACCAC[A/G]TATTTTGCAAGTAAG | 672 |
rs80357164 | snp | A/C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115745 | CCTGTCTCCACAAAG[A/C/G/T]GTGACCACATATTTT | 672 |
rs80357166 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093568 | ATAAAGAAAAAAAAG[G/T]ACAACCAAATGCCAG | 672 |
rs80357167 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094066 | GGAGCATTTGTTACT[A/G/T]AGCCACAGATAATAC | 672 |
rs80357168 | snp | C/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092511 | ACTTTGAGGAACATT[C/G]AATGTCACCTGAAAG | 672 |
rs80357169 | snp | A/G | 4.95356e-05 | 0.00497648 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43067689 | TAATTTCAGATGCTC[A/G]TGTACAAGTTTGCCA | 672 |
rs80357170 | snp | A/C/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092854 | CACTCTGGGTCCTTA[A/C/T]AGAAACAAAGTCCAA | 672 |
rs80357171 | snp | A/G | 3.33539e-05 | 0.00408361 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43063337 | AAAGAAAAATGCTGA[A/G]TGAGGTAAGTACTTG | 672 |
rs80357172 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092271 | CTATGCTTAGATTAG[C/G]GGTTTTGCAACCTGA | 672 |
rs80357173 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093930 | CTGAAATGATAAATC[A/G]GGGAACTAACCAAAC | 672 |
rs80357174 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104900 | AGCTATTGAAAATCA[C/T]TTGTGCTTTTCAGCT | 672 |
rs80357175 | snp | A/G | 3.29717e-05 | 0.00406015 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092077 | TCTGAGACACCTGAT[A/G]ACCTGTTAGATGATG | 672 |
rs80357176 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094537 | ACATGTAATGATAGG[C/T]GGACTCCCAGCACAG | 672 |
rs80357178 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091474 | GGAACGGGCTTGGAA[G/T]AAAATAATCAAGAAG | 672 |
rs80357180 | snp | C/G/T | | | missense, stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099859 | ACCAGTCTCAGTGTC[C/G/T]AACTCTCTAACCTTG | 672 |
rs80357181 | snp | A/G | 1.64827e-05 | 0.00287073 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094170 | CCAAATCAGTAGAGA[A/G]TAATATTGAAGACAA | 672 |
rs80357182 | snp | A/C/T | 0.000148389 | 0.00861234 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43093408 | CAAATGCACCTGGTT[A/C/T]TTTTACTAAGTGTTC | 672 |
rs80357183 | snp | A/T | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045685 | AGATCCCCCACAGCC[A/T]CTACTGACTGCAGCC | 672 |
rs80357184 | snp | A/C | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43092352 | GCTCCAGTATTAATG[A/C]AATAGGTTCCAGTGA | 672 |
rs80357185 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093049 | AGAAATGACACAGAA[A/G]GCTTTAAGTATCCAT | 672 |
rs80357186 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093094 | TTTGAAAACCCCAAG[G/T]GACTAATTCATGGTT | 672 |
rs80357187 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071125 | AACATACCATCTTCA[A/G]CCTCTGCATTGAAAG | 672 |
rs80357188 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092845 | TCCTTAAAGAAACAA[A/T]GTCCAAAAGTCACTT | 672 |
rs80357189 | snp | A/G/T | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43104183 | TTTCTATCATCCAAA[A/G/T]TATGGGCTACAGAAA | 672 |
rs80357190 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104258 | TGTATTTTACAGATG[C/G]AAACAGCTATAATTT | 672 |
rs80357191 | snp | A/G | 0.000181218 | 0.00951714 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091792 | ACTAGGCATAGCACC[A/G]TTGCTACCGAGTGTC | 672 |
rs80357192 | snp | A/G | 1.64882e-05 | 0.00287121 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093411 | TAACAAATGCACCTG[A/G]TTCTTTTACTAAGTG | 672 |
rs80357193 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093567 | TAAAGAAAAAAAAGT[A/T]CAACCAAATGCCAGT | 672 |
rs80357194 | snp | A/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093232 | AGATCTGTAGAGAGT[A/G/T]GCAGTATTTCATTGG | 672 |
rs80357195 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092990 | AACAAGCATAGAAAT[A/G]GAAGAAAGTGAACTT | 672 |
rs80357196 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094642 | CTCACTAAAGACAGA[A/C/G]TGAATGTAGAAAAGG | 672 |
rs80357197 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094280 | ATTGGACGTTCTAAA[G/T]GAGGTAGATGAATAT | 672 |
rs80357198 | snp | A/G | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124026 | AGAAAATCTTAGAGT[A/G]TCCCATCTGGTAAGT | 672 |
rs80357199 | snp | C/G | 0.000247502 | 0.0111216 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43094692 | GCACAAATACTCATG[C/G]CAGCTCATTACAGCA | 672 |
rs80357200 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092863 | TTCTCTGCCCACTCT[A/G]GGTCCTTAAAGAAAC | 672 |
rs80357201 | snp | C/T | 0.000511269 | 0.0159804 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092235 | ATAAACAAAGTCTTC[C/T]TGGAAGTAATTGTAA | 672 |
rs80357202 | snp | A/G/T | 8.24083e-05 | 0.00641852 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43091477 | AGAGGAACGGGCTTG[A/G/T]AAGAAAATAATCAAG | 672 |
rs80357203 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093134 | AAAAACAGAACCAAA[A/T]AAATGTGTGAGTCAG | 672 |
rs80357204 | snp | A/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067683 | CAGATGCTCGTGTAC[A/T]AGTTTGCCAGAAAAC | 672 |
rs80357205 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067694 | TGATTTAATTTCAGA[A/T]GCTCGTGTACAAGTT | 672 |
rs80357206 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092016 | AAAATGACATTAAGG[A/G]AAGTTCTGCTGTTTT | 672 |
rs80357207 | snp | A/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104172 | CAAAGTATGGGCTAC[A/T]GAAACCGTGCCAAAA | 672 |
rs80357208 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091714 | AATGACTGCAGTAAC[C/T]AGGTAATATTGGCAA | 672 |
rs80357209 | snp | C/G/T | 4.94613e-05 | 0.00497275 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43104939 | GCCTACAAGAAAGTA[C/G/T]GAGATTTAGTCAACT | 672 |
rs80357210 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091491 | CAGATGATGAAGAAA[A/G]AGGAACGGGCTTGGA | 672 |
rs80357211 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094582 | GGCTTAGCAAGGAGC[C/T]AACATAACAGATGGG | 672 |
rs80357212 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047643 | GACAATGGCTTCCAT[A/G]GTAAGGTGCCTGCAT | 672 |
rs80357213 | snp | A/C/T | 3.29489e-05 | 0.00405874 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43091653 | AAACAAAATGTTCTG[A/C/T]TAGCTTGTTTTCTTC | 672 |
rs80357214 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094739 | AAAGTATCAGGGTAG[G/T]TCTGTTTCAAACTTG | 672 |
rs80357215 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094465 | AAAGAATGGAATAAG[C/T]AGAAACTGCCATGCT | 672 |
rs80357216 | snp | C/T | | | missense, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047684 | TCCACCCAATTGTGG[C/T]TGTGCAGCCAGATGC | 672 |
rs80357217 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091686 | CAAAGGCATCTCAGG[A/T]ACATCACCTTAGTGA | 672 |
rs80357218 | snp | A/C/G | 1.64871e-05 | 0.00287111 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43091450 | CAAGAAGAGCAAAGC[A/C/G]TGGATTCAAACTTAG | 672 |
rs80357219 | snp | A/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049182 | TAGATCAACTGGAAT[A/G]GATGGTACAGCTGTG | 672 |
rs80357220 | snp | A/G/T | 1.65195e-05 | 0.00287393 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43093712 | AATTCAAAAGCACCT[A/G/T]AAAAGAATAGGCTGA | 672 |
rs80357221 | snp | A/G | 6.59109e-05 | 0.0057403 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094147 | GAAGACAAAATATTT[A/G]GGAAAACCTATCGGA | 672 |
rs80357222 | snp | A/C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063883 | GGAAAATGGGTAGTT[A/C/T]GCTATTTCTGTAAGT | 672 |
rs80357223 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092731 | TTTCCTGTGGTTGGT[C/T]AGAAAGATAAGCCAG | 672 |
rs80357224 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094011 | TAAAGCGTAAAAGGA[G/T]ACCTACATCAGGCCT | 672 |
rs80357225 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094758 | CAGCTGAGAGGCATC[C/G]AGAAAAGTATCAGGG | 672 |
rs80357227 | snp | A/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057113 | TTGAAGTCAGAGGAG[A/G/T]TGTGGTCAATGGAAG | 672 |
rs80357228 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092115 | AACAGCCTATGGGAA[G/T]TAGTCATGCATCTCA | 672 |
rs80357229 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074397 | GTTGATGTGGAGGAG[C/T]AACAGCTGGAAGAGT | 672 |
rs80357230 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092899 | TCAAATCCAGGAAAT[A/G]CAGAAGAGGAATGTG | 672 |
rs80357231 | snp | A/C | 1.64798e-05 | 0.00287047 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43091486 | GATGAAGAAAGAGGA[A/C]CGGGCTTGGAAGAAA | 672 |
rs80357233 | snp | C/G | 1.64914e-05 | 0.00287149 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43093393 | CTTTTACTAAGTGTT[C/G]AAATACCAGTGAACT | 672 |
rs80357234 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104949 | AATTTCAGGAGCCTA[C/T]AAGAAAGTACGAGAT | 672 |
rs80357235 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094410 | ATGTTCCTTGGATAA[C/T]ACTAAATAGCAGCAT | 672 |
rs80357236 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093705 | AAGCACCTAAAAAGA[A/G]TAGGCTGAGGAGGAA | 672 |
rs80357237 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074427 | TACCCATCTCAAGAG[A/G]AGCTCATTAAGGTTG | 672 |
rs80357238 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093536 | CAGGCACAGCAGAAA[C/G]CTACAACTCATGGAA | 672 |
rs80357239 | snp | A/G/T | | | stop-gained, missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063372 | TATGATCTCTTTAGG[A/G/T]GTGACCCAGTCTATT | 672 |
rs80357240 | snp | A/G/T | 1.64808e-05 | 0.00287057 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43093112 | GTGAGTCAGTGTGCA[A/G/T]CATTTGAAAACCCCA | 672 |
rs80357241 | snp | C/G | 3.29549e-05 | 0.00405911 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43047694 | ATCCAGGGTGTCCAC[C/G]CAATTGTGGTTGTGC | 672 |
rs80357243 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063885 | GAGGAAAATGGGTAG[G/T]TAGCTATTTCTGTAA | 672 |
rs80357244 | snp | A/C/G/T | 0.000198344 | 0.00995653 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline)/C(germline) | 17:43094720 | GTTTCAAACTTGCAT[A/C/G/T]TGGAGCCATGTGGCA | 672 |
rs80357245 | snp | A/G | 1.65138e-05 | 0.00287343 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093697 | AAAAAGAATAGGCTG[A/G]GGAGGAAGTCTTCTA | 672 |
rs80357246 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094467 | GAAAAGAATGGAATA[A/G]GCAGAAACTGCCATG | 672 |
rs80357247 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092094 | ATGCATCTCAGGTTT[A/C/G]TTCTGAGACACCTGA | 672 |
rs80357248 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074385 | GAGCAACAGCTGGAA[G/T]AGTCTGGGCCACACG | 672 |
rs80357249 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093057 | AAGATAATAGAAATG[A/T]CACAGAAGGCTTTAA | 672 |
rs80357250 | snp | C/T | 1.64802e-05 | 0.00287051 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093529 | AGCAGAAACCTACAA[C/T]TCATGGAAGGTAAAG | 672 |
rs80357251 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092896 | AATCCAGGAAATGCA[A/G/T]AAGAGGAATGTGCAA | 672 |
rs80357252 | snp | A/C/G | 4.94197e-05 | 0.00497066 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43094567 | CAACATAACAGATGG[A/C/G]CTGGAAGTAAGGAAA | 672 |
rs80357253 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094309 | TCTGAATCAAATGCC[A/G]AAGTAGCTGATGTAT | 672 |
rs80357254 | snp | A/G/T | 1.64746e-05 | 0.00287002 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43091663 | CTTAGTGAGGAAACA[A/G/T]AATGTTCTGCTAGCT | 672 |
rs80357255 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094221 | TGGCCAGTGATCCTC[A/C]TGAGGCTTTAATATG | 672 |
rs80357256 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092742 | TCACTGCAGGCTTTC[C/T]TGTGGTTGGTCAGAA | 672 |
rs80357257 | snp | A/C/G/T | 3.29491e-05 | 0.00405877 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43091602 | ACTTGACTGCAAATA[A/C/G/T]AAACACCCAGGATCC | 672 |
rs80357258 | snp | A/G | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045712 | AGGAGCTGGACACCT[A/G]CCTGATACCCCAGAT | 672 |
rs80357259 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091012 | GCAGCATCTGGGTGT[G/T]AGAGTGAAACAAGCG | 672 |
rs80357260 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090946 | GACATTTTAACCACT[C/T]AGGTAAAAAGCGTGT | 672 |
rs80357261 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070957 | AAAAGAATGTCCATG[A/G]TGGTGTCTGGCCTGA | 672 |
rs80357262 | snp | C/T | 1.64749e-05 | 0.00287005 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091564 | ATTGGTTCTTCCAAA[C/T]AAATGAGGCATCAGT | 672 |
rs80357263 | snp | A/G | 1.64798e-05 | 0.00287047 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092311 | CAAGCAGAACTAGGT[A/G]GAAACAGAGGGCCAA | 672 |
rs80357264 | snp | A/G | 0.000131778 | 0.00811614 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43099813 | TGAGGACAAAGCAGC[A/G]GATACAACCTCAAAA | 672 |
rs80357265 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067637 | CTAATCTAATTACTG[A/T]AGAGACTACTCATGT | 672 |
rs80357266 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115777 | CCTACCCTGCTAGTC[C/T]GGAGTTGATCAAGGA | 672 |
rs80357267 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093615 | CTAATTGTACTGAAT[A/T]GCAAATTGATAGTTG | 672 |
rs80357268 | snp | A/G | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045773 | TGTGAGGCACCTGTG[A/G]TGACCCGAGAGTGGG | 672 |
rs80357269 | snp | A/C/T | | | stop-gained, missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091746 | AGGAGAATTTATTAT[A/C/T]ATTGAAGAATAGCTT | 672 |
rs80357270 | snp | A/G/T | 6.58907e-05 | 0.00573948 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43057131 | GTTTCTTTCAGCATG[A/G/T]TTTTGAAGTCAGAGG | 672 |
rs80357271 | snp | A/G | 4.9436e-05 | 0.00497148 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092401 | GCCAGCTCAAGCAAT[A/G]TTAATGAAGTAGGTT | 672 |
rs80357272 | snp | C/T | 0.000181337 | 0.00952028 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092083 | GTTTGTTCTGAGACA[C/T]CTGATGACCTGTTAG | 672 |
rs80357273 | snp | A/G | 1.65619e-05 | 0.00287762 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093958 | AAAGCAGATTTGGCA[A/G]TTCAAAAGACTCCTG | 672 |
rs80357274 | snp | C/T | 3.30573e-05 | 0.00406541 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43045704 | GACACCTACCTGATA[C/T]CCCAGATCCCCCACA | 672 |
rs80357275 | snp | C/T | 1.6473e-05 | 0.00286988 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43099867 | AGCAGGAAACCAGTC[C/T]CAGTGTCCAACTCTC | 672 |
rs80357276 | snp | A/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115738 | CCACAAAGTGTGACC[A/G/T]CATATTTTGCAAGTA | 672 |
rs80357277 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074388 | GAGGAGCAACAGCTG[G/T]AAGAGTCTGGGCCAC | 672 |
rs80357278 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092191 | AAAAAGCAAGAATAT[G/T]AAGAAGTAGTTCAGA | 672 |
rs80357279 | snp | A/C/T | 1.64773e-05 | 0.00287026 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43094132 | GGGAAAACCTATCGG[A/C/T]AGAAGGCAAGCCTCC | 672 |
rs80357280 | snp | A/G | 0.00023062 | 0.0107358 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091708 | TGCAGTAACCAGGTA[A/G]TATTGGCAAAGGCAT | 672 |
rs80357281 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051104 | AGATCTTCAGGGGGC[C/T]AGAAATCTGTTGCTA | 672 |
rs80357282 | snp | A/C/T | 1.65067e-05 | 0.00287282 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43093691 | AATAGGCTGAGGAGG[A/C/T]AGTCTTCTACCAGGC | 672 |
rs80357283 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057114 | TTTGAAGTCAGAGGA[G/T]ATGTGGTCAATGGAA | 672 |
rs80357284 | snp | A/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049181 | AGATCAACTGGAATG[A/G]ATGGTACAGCTGTGT | 672 |
rs80357285 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092941 | AATACATTCAAGGTT[G/T]CAAAGCGCCAGTCAT | 672 |
rs80357286 | snp | A/G | 6.58946e-05 | 0.0057396 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43047654 | CCTGGACAGAGGACA[A/G]TGGCTTCCATGGTAA | 672 |
rs80357287 | snp | A/G | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124096 | TTGGAACAGAAAGAA[A/G]TGGATTTATCTGCTC | 672 |
rs80357288 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092218 | GGAAGTAATTGTAAG[A/C]ATCCTGAAATAAAAA | 672 |
rs80357290 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091950 | GTCCTAGCCCTTTCA[C/T]CCATACACATTTGGC | 672 |
rs80357291 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063353 | ACCCAGTCTATTAAA[G/T]AAAGAAAAATGCTGA | 672 |
rs80357292 | snp | A/G | 1.64741e-05 | 0.00286998 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094569 | GCCAACATAACAGAT[A/G]GGCTGGAAGTAAGGA | 672 |
rs80357293 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094774 | ACCACTGAGAAGCGT[A/G]CAGCTGAGAGGCATC | 672 |
rs80357294 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091918 | CAGGGTTACCGAAGA[A/C/G]GGGCCAAGAAATTAG | 672 |
rs80357295 | snp | A/C | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092667 | CTAGGTTTTGTCTAT[A/C]ATCTCAGTTCAGAGG | 672 |
rs80357296 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091987 | TTTAGCAAAAGCGTC[C/T]AGAAAGGAGAGCTTA | 672 |
rs80357297 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092121 | ACTTAGAACAGCCTA[C/T]GGGAAGTAGTCATGC | 672 |
rs80357298 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093426 | TCCCAGAGCTGAAGT[G/T]AACAAATGCACCTGG | 672 |
rs80357299 | snp | A/C | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045749 | GAGTGGGTGTTGGAC[A/C]GTGTAGCACTCTACC | 672 |
rs80357301 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094300 | AATGCCAAAGTAGCT[A/G]ATGTATTGGACGTTC | 672 |
rs80357302 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070973 | AACAGAAAGGGTCAA[A/C]AAAAGAATGTCCATG | 672 |
rs80357303 | snp | A/C/T | 1.6473e-05 | 0.00286988 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43071113 | TCAACCTCTGCATTG[A/C/T]AAGTTCCCCAATTGA | 672 |
rs80357304 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094081 | GAAAATCTAATTATA[G/T]GAGCATTTGTTACTG | 672 |
rs80357305 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082503 | GAAGCTGTGTTAGAA[C/T]AGCATGGGAGCCAGC | 672 |
rs80357306 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082563 | AAGCAGAGGGATACC[A/G]TGCAACATAACCTGA | 672 |
rs80357307 | snp | A/G | | | stop-gained, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045760 | TGGTGACCCGAGAGT[A/G]GGTGTTGGACAGTGT | 672 |
rs80357309 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082506 | CTAGAAGCTGTGTTA[C/G]AACAGCATGGGAGCC | 672 |
rs80357310 | snp | C/G | 1.64827e-05 | 0.00287073 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43091870 | TTATCTAGTGAGGAT[C/G]AAGAGCTTCCCTGCT | 672 |
rs80357311 | snp | A/G | 1.64836e-05 | 0.0028708 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092476 | ATGGGAAATGAGAAC[A/G]TTCCAAGTACAGTGA | 672 |
rs80357312 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104231 | ATTTTGCAAAAAAGG[A/C]AAATAACTCTCCTGA | 672 |
rs80357313 | snp | C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092304 | AACTAGGTAGAAACA[C/G/T]AGGGCCAAAATTGAA | 672 |
rs80357314 | snp | C/T | 1.65214e-05 | 0.0028741 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43067691 | TTTAATTTCAGATGC[C/T]CGTGTACAAGTTTGC | 672 |
rs80357315 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092970 | AAAGTGAACTTGATG[C/T]TCAGTATTTGCAGAA | 672 |
rs80357316 | snp | C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124053 | AAGTACAAAATGTCA[C/T]TAATGCTATGCAGAA | 672 |
rs80357317 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092222 | TCCTGGAAGTAATTG[A/T]AAGCATCCTGAAATA | 672 |
rs80357318 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091594 | GCAAATACAAACACC[C/T]AGGATCCTTTCTTGA | 672 |
rs80357321 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094748 | GCATCCAGAAAAGTA[G/T]CAGGGTAGTTCTGTT | 672 |
rs80357322 | snp | C/G | 4.96307e-05 | 0.00498125 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43045694 | TGATACCCCAGATCC[C/G]CCACAGCCACTACTG | 672 |
rs80357323 | snp | C/G/T | 8.24608e-05 | 0.00642065 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43045739 | TGGACAGTGTAGCAC[C/G/T]CTACCAGTGCCAGGA | 672 |
rs80357324 | snp | A/T | 1.65652e-05 | 0.0028779 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43051078 | TGCTATGGGCCCTTC[A/T]CCAACATGCCCACAG | 672 |
rs80357325 | snp | C/T | 1.6473e-05 | 0.00286988 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43099814 | CTGAGGACAAAGCAG[C/T]GGATACAACCTCAAA | 672 |
rs80357326 | snp | A/C | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045717 | GTGCCAGGAGCTGGA[A/C]ACCTACCTGATACCC | 672 |
rs80357327 | snp | A/C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115730 | TGTGACCACATATTT[A/C/G/T]GCAAGTAAGTTTGAA | 672 |
rs80357328 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093058 | AAAGATAATAGAAAT[G/T]ACACAGAAGGCTTTA | 672 |
rs80357329 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092124 | ATAACTTAGAACAGC[C/G]TATGGGAAGTAGTCA | 672 |
rs80357331 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094709 | GCATGTGGAGCCATG[A/T]GGCACAAATACTCAT | 672 |
rs80357332 | snp | G/T | 1.64768e-05 | 0.00287021 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43045792 | TCCAGCAATTGGGCA[G/T]ATGTGTGAGGCACCT | 672 |
rs80357333 | snp | C/T | 1.65658e-05 | 0.00287795 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093960 | AGAAAGCAGATTTGG[C/T]AGTTCAAAAGACTCC | 672 |
rs80357334 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092177 | TGAAGAAGTAGTTCA[G/T]ACTGTTAATACAGAT | 672 |
rs80357335 | snp | A/G | 3.29957e-05 | 0.00406162 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093348 | ATCCTAGCCTTCCAA[A/G]AGAAGAAAAAGAAGA | 672 |
rs80357336 | snp | A/C/G | | | stop-gained, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045711 | GGAGCTGGACACCTA[A/C/G]CTGATACCCCAGATC | 672 |
rs80357337 | snp | A/G | 8.24124e-05 | 0.00641868 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093009 | AAGTTAACCACAGTC[A/G]GGAAACAAGCATAGA | 672 |
rs80357338 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094486 | GCTGATCCCCTGTGT[G/T]AGAGAAAAGAATGGA | 672 |
rs80357340 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057112 | TGAAGTCAGAGGAGA[G/T]GTGGTCAATGGAAGA | 672 |
rs80357341 | snp | A/G | 3.2963e-05 | 0.00405961 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43071148 | CCCCAGAGTCAGCTC[A/G]TGTTGGCAACATACC | 672 |
rs80357343 | snp | A/C/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091567 | TTGATTGGTTCTTCC[A/C/G/T]AACAAATGAGGCATC | 672 |
rs80357344 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093607 | ACTGAATTGCAAATT[C/G]ATAGTTGTTCTAGCA | 672 |
rs80357345 | snp | C/T | 4.94409e-05 | 0.00497172 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091485 | ATGAAGAAAGAGGAA[C/T]GGGCTTGGAAGAAAA | 672 |
rs80357346 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094239 | CAGAGAAAATAGACT[G/T]ACTGGCCAGTGATCC | 672 |
rs80357347 | snp | A/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063347 | TCTATTAAAGAAAGA[A/T]AAATGCTGAATGAGG | 672 |
rs80357349 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071236 | CCATTCCTTTCAGAG[G/T]GAACCCCTTACCTGG | 672 |
rs80357350 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104928 | AGTACGAGATTTAGT[C/T]AACTTGTTGAAGAGC | 672 |
rs80357351 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094809 | CTGAACATCATCAAC[C/T]CAGTAATAATGATTT | 672 |
rs80357352 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071104 | GCATTGAAAGTTCCC[C/T]AATTGAAAGTTGCAG | 672 |
rs80357353 | snp | A/G | 8.23893e-05 | 0.00641778 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43082548 | ATGCAACATAACCTG[A/G]TAAAGCTCCAGCAGG | 672 |
rs80357354 | snp | A/C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082418 | GAAATCCAGAACAAA[A/C/G]CACATCAGAAAAAGG | 672 |
rs80357355 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093571 | GAGATAAAGAAAAAA[A/G/T]AGTACAACCAAATGC | 672 |
rs80357356 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091867 | TCTAGTGAGGATGAA[G/T]AGCTTCCCTGCTTCC | 672 |
rs80357357 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104165 | TGGGCTACAGAAACC[A/G]TGCCAAAAGACTTCT | 672 |
rs80357358 | snp | C/T | | | missense, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047687 | GTGTCCACCCAATTG[C/T]GGTTGTGCAGCCAGA | 672 |
rs80357360 | snp | C/T | 1.64789e-05 | 0.0028704 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094164 | CAGTAGAGAGTAATA[C/T]TGAAGACAAAATATT | 672 |
rs80357361 | snp | A/G | 1.64792e-05 | 0.00287042 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092773 | TCTAATATCAAGCCT[A/G]TACAGACAGTTAATA | 672 |
rs80357362 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091771 | ACCGAGTGTCTGTCT[A/G]AGAACACAGAGGAGA | 672 |
rs80357364 | snp | C/T | 6.59359e-05 | 0.00574139 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093144 | TAGGGAAGGCAAAAA[C/T]AGAACCAAATAAATG | 672 |
rs80357365 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082557 | AGGGATACCATGCAA[C/T]ATAACCTGATAAAGC | 672 |
rs80357366 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074403 | AAGGTTGTTGATGTG[G/T]AGGAGCAACAGCTGG | 672 |
rs80357367 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057090 | AATGGAAGAAACCAC[C/T]AAGGTCCAAAGCGAG | 672 |
rs80357368 | snp | A/G | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045748 | AGTGGGTGTTGGACA[A/G]TGTAGCACTCTACCA | 672 |
rs80357369 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092101 | AGTAGTCATGCATCT[C/T]AGGTTTGTTCTGAGA | 672 |
rs80357370 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106529 | ATAATTTATAGATTT[G/T]GCATGCTGAAACTTC | 672 |
rs80357371 | snp | C/G/T | 4.95522e-05 | 0.00497736 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43093745 | ATAAGCAATATGGAA[C/G/T]TCGAATTAAATATCC | 672 |
rs80357372 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104148 | GCCAAAAGACTTCTA[C/T]AGAGTGAACCCGAAA | 672 |
rs80357373 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070979 | AGCTTCAACAGAAAG[C/G]GTCAACAAAAGAATG | 672 |
rs80357374 | snp | A/C/T | 0.000181895 | 0.0095349 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43093915 | AGGGAACTAACCAAA[A/C/T]GGAGCAGAATGGTCA | 672 |
rs80357376 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094059 | TTGTTACTGAGCCAC[A/C/G]GATAATACAAGAGCG | 672 |
rs80357377 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092770 | AATATCAAGCCTGTA[C/T]AGACAGTTAATATCA | 672 |
rs80357379 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074441 | TTCAGAATAGAAACT[A/G]CCCATCTCAAGAGGA | 672 |
rs80357381 | snp | A/G/T | 1.64833e-05 | 0.00287078 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43093128 | AGAACCAAATAAATG[A/G/T]GTGAGTCAGTGTGCA | 672 |
rs80357382 | snp | A/G | | | missense, intron-variant | BRCA1 | GRCh38.p7 | 17:43106457 | AATGATATAACCAAA[A/G]GGTATATAATTTGGT | 672 |
rs80357383 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074502 | TCCCCTTCTAAATGC[C/T]CATCATTAGATGATA | 672 |
rs80357384 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099832 | CTTGGAACTGTGAGA[A/C]CTCTGAGGACAAAGC | 672 |
rs80357385 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094390 | AATAGCAGCATTCAG[A/T]AAGTTAATGAGTGGT | 672 |
rs80357386 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092451 | CAGTGAGCACAATTA[A/G]CCGTAATAACATTAG | 672 |
rs80357387 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063941 | TGCAGATGCTGAGTT[A/T]GTGTGTGAACGGACA | 672 |
rs80357388 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091820 | TAAAGTAAACAATAT[A/G]CCTTCTCAGTCTACT | 672 |
rs80357389 | snp | A/G/T | 1.648e-05 | 0.0028705 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43076488 | AACCAGGAGTGGAAA[A/G/T]GTAAGAAACATCAAT | 672 |
rs80357390 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070950 | TGTCCATGGTGGTGT[C/T]TGGCCTGACCCCAGA | 672 |
rs80357391 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093514 | CTCATGGAAGGTAAA[G/T]AACCTGCAACTGGAG | 672 |
rs80357392 | snp | C/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094731 | AGGGTAGTTCTGTTT[C/G]AAACTTGCATGTGGA | 672 |
rs80357393 | snp | A/G | 1.64776e-05 | 0.00287028 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43045782 | GGGCAGATGTGTGAG[A/G]CACCTGTGGTGACCC | 672 |
rs80357394 | snp | C/G | 0.000176323 | 0.00938779 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43095904 | GGGAGATCAAGAATT[C/G]TTACAAATCACCCCT | 672 |
rs80357396 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094815 | CAAATACTGAACATC[A/G]TCAACCCAGTAATAA | 672 |
rs80357397 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091006 | TCTGGGTGTGAGAGT[G/T]AAACAAGCGTCTCTG | 672 |
rs80357398 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094401 | GGATAACACTAAATA[A/G]CAGCATTCAGAAAGT | 672 |
rs80357399 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093181 | ACTCAGGAAAGTATC[G/T]CGTTACTGGAAGTTA | 672 |
rs80357400 | snp | A/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094073 | AATTATAGGAGCATT[A/G/T]GTTACTGAGCCACAG | 672 |
rs80357401 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070933 | GGCCTGACCCCAGAA[G/T]AATTTGTGAGTGTAT | 672 |
rs80357402 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092263 | AGATTAGGGGTTTTG[C/T]AACCTGAGGTCTATA | 672 |
rs80357404 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076522 | GTGTCTGCAGATAGT[A/T]CTACCAGTAAAAATA | 672 |
rs80357405 | snp | C/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092142 | CTCCATATCTGATTT[C/G]AGATAACTTAGAACA | 672 |
rs80357406 | snp | A/G | 1.65225e-05 | 0.00287419 | BRCA1, NBR2 | 17 | allele_origin=G(germline)/A(germline) | 17:43124036 | AATGCTATGCAGAAA[A/G]TCTTAGAGTGTCCCA | 672 |
rs80357407 | snp | A/G | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091495 | GTTTCAGATGATGAA[A/G]AAAGAGGAACGGGCT | 672 |
rs80357409 | snp | C/G/T | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43104877 | TTTCAGCTTGACACA[C/G/T]GTTTGGAGTGTAAGT | 672 |
rs80357410 | snp | C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124027 | CAGAAAATCTTAGAG[C/T]GTCCCATCTGGTAAG | 672 |
rs80357411 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071175 | CTGAATCTGATCCTT[C/T]TGAAGACAGAGCCCC | 672 |
rs80357413 | snp | A/C | 3.29462e-05 | 0.00405857 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43104167 | TATGGGCTACAGAAA[A/C]CGTGCCAAAAGACTT | 672 |
rs80357414 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070947 | CCATGGTGGTGTCTG[A/G]CCTGACCCCAGAAGA | 672 |
rs80357415 | snp | C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093313 | CTAGAAACAGTTAAA[C/G/T]TGTCTAATAATGCTG | 672 |
rs80357416 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094425 | CTAGAGATACTGAAG[A/G]TGTTCCTTGGATAAC | 672 |
rs80357417 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094265 | TGAGGTAGATGAATA[G/T]TCTGGTTCTTCAGAG | 672 |
rs80357418 | snp | A/G | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063890 | TGCGGGAGGAAAATG[A/G]GTAGTTAGCTATTTC | 672 |
rs80357419 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092791 | AATCAAGGAAAGAAT[G/T]AGTCTAATATCAAGC | 672 |
rs80357420 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092839 | AAGAAACAAAGTCCA[A/G]AAGTCACTTTTGAAT | 672 |
rs80357421 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092192 | AAAAAAGCAAGAATA[G/T]GAAGAAGTAGTTCAG | 672 |
rs80357424 | snp | C/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092353 | GGCTCCAGTATTAAT[C/G/T]AAATAGGTTCCAGTG | 672 |
rs80357425 | snp | A/G | 3.29843e-05 | 0.00406092 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093652 | GCGCTTGAACTAGTA[A/G]TCAGTAGAAATCTAA | 672 |
rs80357426 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093337 | CCAAGAGAAGAAAAA[G/T]AAGAGAAACTAGAAA | 672 |
rs80357427 | snp | C/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094002 | AAAGGAGACCTACAT[C/G]AGGCCTTCATCCTGA | 672 |
rs80357428 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051077 | GCTATGGGCCCTTCA[C/T]CAACATGCCCACAGG | 672 |
rs80357429 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071127 | GCAACATACCATCTT[C/T]AACCTCTGCATTGAA | 672 |
rs80357431 | snp | A/C/T | 3.29583e-05 | 0.00405934 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43074349 | ACGGAAACATCTTAC[A/C/T]TGCCAAGGCAAGATC | 672 |
rs80357432 | snp | A/C/G/T | 6.58892e-05 | 0.00573936 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43057069 | CCAAAGCGAGCAAGA[A/C/G/T]AATCCCAGGACAGAA | 672 |
rs80357433 | snp | C/G | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071225 | AGAGGGAACCCCTTA[C/G]CTGGAATCTGGAATC | 672 |
rs80357434 | snp | C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092103 | GAAGTAGTCATGCAT[C/G/T]TCAGGTTTGTTCTGA | 672 |
rs80357435 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093004 | AACCACAGTCGGGAA[A/G]CAAGCATAGAAATGG | 672 |
rs80357436 | snp | A/C/G | 3.30202e-05 | 0.00406313 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43094704 | TGGAGCCATGTGGCA[A/C/G]AAATACTCATGCCAG | 672 |
rs80357437 | snp | A/C | 1.65211e-05 | 0.00287407 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43074498 | CTTCTAAATGCCCAT[A/C]ATTAGATGATAGGTG | 672 |
rs80357438 | snp | C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124032 | CTATGCAGAAAATCT[C/T]AGAGTGTCCCATCTG | 672 |
rs80357439 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071103 | CATTGAAAGTTCCCC[A/G]ATTGAAAGTTGCAGA | 672 |
rs80357440 | snp | A/C/G/T | 1.6476e-05 | 0.00287014 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43091638 | CTAGCTTGTTTTCTT[A/C/G/T]ACAGTGCAGTGAATT | 672 |
rs80357441 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093445 | AGACATGACAGCGAT[A/G]CTTTCCCAGAGCTGA | 672 |
rs80357442 | snp | A/C/G | 4.94173e-05 | 0.00497053 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43057077 | ACCAAGGTCCAAAGC[A/C/G]AGCAAGAGAATCCCA | 672 |
rs80357443 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115775 | TACCCTGCTAGTCTG[G/T]AGTTGATCAAGGAAC | 672 |
rs80357444 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093200 | ACCTGGTACTGATTA[A/T]GGCACTCAGGAAAGT | 672 |
rs80357445 | snp | C/T | 1.65031e-05 | 0.00287251 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094021 | ACAAATAAATTAAAG[C/T]GTAAAAGGAGACCTA | 672 |
rs80357446 | snp | A/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115729 | GTGACCACATATTTT[A/G/T]CAAGTAAGTTTGAAT | 672 |
rs80357448 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104193 | AAAGATGAAGTTTCT[A/G]TCATCCAAAGTATGG | 672 |
rs80357449 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093238 | ACTGAAAGATCTGTA[G/T]AGAGTAGCAGTATTT | 672 |
rs80357450 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057116 | ATTTTGAAGTCAGAG[A/G]AGATGTGGTCAATGG | 672 |
rs80357451 | snp | C/G/T | | | missense, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047681 | ACCCAATTGTGGTTG[C/G/T]GCAGCCAGATGCCTG | 672 |
rs80357452 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093731 | ACTCGAATTAAATAT[C/G]CACAATTCAAAAGCA | 672 |
rs80357453 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093967 | TTTATCAAGAAAGCA[A/G]ATTTGGCAGTTCAAA | 672 |
rs80357454 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093763 | GAACCTATAAGCAGC[A/G]GTATAAGCAATATGG | 672 |
rs80357455 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091912 | TACCGAAGAGGGGCC[A/G/T]AGAAATTAGAGTCCT | 672 |
rs80357456 | snp | C/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091456 | AATAATCAAGAAGAG[C/G/T]AAAGCATGGATTCAA | 672 |
rs80357457 | snp | A/C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104166 | ATGGGCTACAGAAAC[A/C/T]GTGCCAAAAGACTTC | 672 |
rs80357458 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092699 | TGATAATGCCAAATG[A/T]AGTATCAAAGGAGGC | 672 |
rs80357459 | snp | A/G/T | 0.000346018 | 0.0131487 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43092448 | TGAGCACAATTAGCC[A/G/T]TAATAACATTAGAGA | 672 |
rs80357460 | snp | C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092766 | TCAAGCCTGTACAGA[C/G/T]AGTTAATATCACTGC | 672 |
rs80357461 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091627 | TCTTCACAGTGCAGT[A/G/T]AATTGGAAGACTTGA | 672 |
rs80357462 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057083 | GAAACCACCAAGGTC[C/G]AAAGCGAGCAAGAGA | 672 |
rs80357463 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051098 | TCAGGGGGCTAGAAA[G/T]CTGTTGCTATGGGCC | 672 |
rs80357464 | snp | A/G | 4.94205e-05 | 0.0049707 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094536 | CATGTAATGATAGGC[A/G]GACTCCCAGCACAGA | 672 |
rs80357465 | snp | A/G | 1.64732e-05 | 0.0028699 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43071032 | GCTGGGTATAATGCA[A/G]TGGAAGAAAGTGTGA | 672 |
rs80357466 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082473 | CCTTCTAACAGCTAC[C/T]CTTCCATCATAAGTG | 672 |
rs80357467 | snp | C/T | 0.00019771 | 0.00994062 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093216 | GCAGTATTTCATTGG[C/T]ACCTGGTACTGATTA | 672 |
rs80357468 | snp | A/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094415 | TGAAGATGTTCCTTG[A/G]ATAACACTAAATAGC | 672 |
rs80357470 | snp | C/G | 4.94849e-05 | 0.00497393 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43074486 | CATCATTAGATGATA[C/G]GTGGTACATGCACAG | 672 |
rs80357471 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106490 | AAGAAAGGGCCTTCA[C/T]AGTGTCCTTTATGTA | 672 |
rs80357472 | snp | G/T | 3.29489e-05 | 0.00405874 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43094477 | CTGTGTGAGAGAAAA[G/T]AATGGAATAAGCAGA | 672 |
rs80357473 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082562 | AGCAGAGGGATACCA[C/T]GCAACATAACCTGAT | 672 |
rs80357474 | snp | C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049188 | CCATTTTAGATCAAC[C/G/T]GGAATGGATGGTACA | 672 |
rs80357475 | snp | G/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124094 | GGAACAGAAAGAAAT[G/T]GATTTATCTGCTCTT | 672 |
rs80357477 | snp | A/G | | | missense, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047657 | ATGCCTGGACAGAGG[A/G]CAATGGCTTCCATGG | 672 |
rs80357478 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092620 | ATTACTCCAAATAAA[A/C]ATGGACTTTTACAAA | 672 |
rs80357479 | snp | A/C/G | 1.64795e-05 | 0.00287045 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43092362 | AATGAAGTGGGCTCC[A/C/G]GTATTAATGAAATAG | 672 |
rs80357480 | snp | C/T | 8.23866e-05 | 0.00641767 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092869 | GCAACATTCTCTGCC[C/T]ACTCTGGGTCCTTAA | 672 |
rs80357481 | snp | A/C/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094317 | ATGGGGAGTCTGAAT[A/C/G]AAATGCCAAAGTAGC | 672 |
rs80357482 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094695 | GTGGCACAAATACTC[A/G]TGCCAGCTCATTACA | 672 |
rs80357483 | snp | A/C | 1.64743e-05 | 0.00287 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43091689 | TGGCAAAGGCATCTC[A/C]GGAACATCACCTTAG | 672 |
rs80357484 | snp | C/G | 1.64846e-05 | 0.0028709 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43092068 | CCTGATGACCTGTTA[C/G]ATGATGGTGAAATAA | 672 |
rs80357485 | snp | A/C/T | 1.64912e-05 | 0.00287147 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092245 | CCTGAGGTCTATAAA[A/C/T]AAAGTCTTCCTGGAA | 672 |
rs80357486 | snp | A/G | 1.64795e-05 | 0.00287045 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43082419 | CGAAATCCAGAACAA[A/G]GCACATCAGAAAAAG | 672 |
rs80357488 | snp | G/T | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43094273 | GTTCTAAATGAGGTA[G/T]ATGAATATTCTGGTT | 672 |
rs80357489 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094083 | CTGAAAATCTAATTA[C/T]AGGAGCATTTGTTAC | 672 |
rs80357490 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094110 | CAAGCCTCCCCAACT[G/T]AAGCCATGTAACTGA | 672 |
rs80357492 | snp | A/C/T | 1.6477e-05 | 0.00287024 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43082541 | ATAACCTGATAAAGC[A/C/T]CCAGCAGGAAATGGC | 672 |
rs80357493 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093950 | TTTGGCAGTTCAAAA[C/G]ACTCCTGAAATGATA | 672 |
rs80357494 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093546 | AAATGCCAGTCAGGC[A/G]CAGCAGAAACCTACA | 672 |
rs80357495 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093647 | TGAACTAGTAGTCAG[G/T]AGAAATCTAAGCCCA | 672 |
rs80357496 | snp | A/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057120 | CATGATTTTGAAGTC[A/T]GAGGAGATGTGGTCA | 672 |
rs80357497 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092608 | AAACATGGACTTTTA[C/T]AAAACCCATATCGTA | 672 |
rs80357498 | snp | A/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115744 | CTGTCTCCACAAAGT[A/G/T]TGACCACATATTTTG | 672 |
rs80357499 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091680 | CATCTCAGGAACATC[A/G]CCTTAGTGAGGAAAC | 672 |
rs80357500 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091587 | CAAACACCCAGGATC[A/C/G]TTTCTTGATTGGTTC | 672 |
rs80357501 | snp | A/G | 0.000116549 | 0.00763289 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43063350 | CAGTCTATTAAAGAA[A/G]GAAAAATGCTGAATG | 672 |
rs80357502 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092551 | TTTGTTAAAACTAAA[-/T]GTAAGAAAAATCTGC | 672 |
rs80357503 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093092 | TGAAAACCCCAAGGG[-/G]ACTAATTCATGGTTG | 672 |
rs80357504 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091599 | TGACTGCAAATACAA[-/A]CACCCAGGATCCTTT | 672 |
rs80357505 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094091 | CCATGTAACTGAAAA[-/A]TCTAATTATAGGAGC | 672 |
rs80357506 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094023 | TCACAAATAAATTAA[-/A]GCGTAAAAGGAGACC | 672 |
rs80357507 | in-del | -/AGAAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093334 | TCCAAGAGAAGAAAA[-/AGAAG]AGAAACTAGAAACAG | 672 |
rs80357508 | in-del | -/TCAA | 3.29696e-05 | 0.00406001 | BRCA1 | 17 | allele_origin=T(germline,somatic)/+.-----(germline) | 17:43091463 | CTTGGAAGAAAATAA[-/TCAA]GAAGAGCAAAGCATG | 672 |
rs80357509 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092046 | GTGAAATAAAGGAAG[-/A]TACTAGTTTTGCTGA | 672 |
rs80357510 | in-del | -/CT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092501 | AACATTCAATGTCAC[-/CT]GAAAGAGAAATGGGA | 672 |
rs80357511 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092337 | AAATAGGTTCCAGTG[-/G]ATGAAAACATTCAAG | 672 |
rs80357512 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091908 | GAAGAGGGGCCAAGA[-/A]AATTAGAGTCCTCAG | 672 |
rs80357513 | in-del | -/TGC | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092883 | TGCAGAAGAGGAATG[-/TGC]AACATTCTCTGCCCA | 672 |
rs80357514 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094289 | AGCTGATGTATTGGA[-/A]CGTTCTAAATGAGGT | 672 |
rs80357515 | in-del | -/TC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093193 | TACTGATTATGGCAC[-/TC]AGGAAAGTATCTCGT | 672 |
rs80357516 | in-del | -/NNNN/TAGT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093653 | TGCGCTTGAACTAGT[-/NNNN/TAGT]AGTCAGTAGAAATCT | 672 |
rs80357517 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092277 | TGAATGCTATGCTTA[-/A]GATTAGGGGTTTTGC | 672 |
rs80357518 | in-del | -/TAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092853 | CCCACTCTGGGTCCT[-/TAAA]GAAACAAAGTCCAAA | 672 |
rs80357519 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092695 | AATGCCAAATGTAGT[-/T]ATCAAAGGAGGCTCT | 672 |
rs80357520 | in-del | -/TA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091771 | TACCGAGTGTCTGTC[-/TA]AGAACACAGAGGAGA | 672 |
rs80357521 | in-del | -/A/GTTTCTCTTCTTTTTCTT | 1.64802e-05 | 0.00287051 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43093529 | AGCAGAAACCTACAA[-/A/GTTTCTCTTCTTTTTCTT]CTCATGGAAGGTAAA | 672 |
rs80357522 | in-del | -/A | 1.6489e-05 | 0.00287128 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43093570 | AGATAAAGAAAAAAA[-/A]GTACAACCAAATGCC | 672 |
rs80357523 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094696 | TGTGGCACAAATACT[-/C]ATGCCAGCTCATTAC | 672 |
rs80357524 | in-del | -/C | 1.64825e-05 | 0.00287071 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43093098 | AGCATTTGAAAACCC[-/C]AAGGGACTAATTCAT | 672 |
rs80357525 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092201 | ATCCTGAAATAAAAA[-/AG]CAAGAATATGAAGAA | 672 |
rs80357526 | in-del | -/GAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093575 | CAGTGAAGAGATAAA[-/GAAA]AAAAAGTACAACCAA | 672 |
rs80357527 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094039 | ATACAAGAGCGTCCC[-/C]TCACAAATAAATTAA | 672 |
rs80357528 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094238 | AGAGAAAATAGACTT[-/T]ACTGGCCAGTGATCC | 672 |
rs80357529 | in-del | -/TG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091018 | AGGTGAAGCAGCATC[-/TG]GGTGTGAGAGTGAAA | 672 |
rs80357530 | in-del | -/AATG | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124057 | GTTGAAGAAGTACAA[-/AATG]TCATTAATGCTATGC | 672 |
rs80357531 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091944 | GCCCTTTCACCCATA[-/A]CACATTTGGCTCAGG | 672 |
rs80357532 | in-del | -/AGAG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090963 | CAGGGCTATCCTCTC[-/AGAG]TGACATTTTAACCAC | 672 |
rs80357533 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092245 | CCTGAGGTCTATAAA[-/C]AAAGTCTTCCTGGAA | 672 |
rs80357534 | in-del | -/CA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074472 | TAGGTGGTACATGCA[-/CA]GTTGCTCTGGGAGTC | 672 |
rs80357535 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094276 | GACGTTCTAAATGAG[-/G]TAGATGAATATTCTG | 672 |
rs80357536 | in-del | -/A/TGTC | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124026 | AGAAAATCTTAGAGT[-/A/TGTC]GTCCCATCTGGTAAG | 672 |
rs80357537 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095847 | GGATTCTGCAAAAAA[-/A]GGGTAATGGCAAAGT | 672 |
rs80357538 | in-del | -/TGAC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090959 | GCTATCCTCTCAGAG[-/TGAC]ATTTTAACCACTCAG | 672 |
rs80357539 | in-del | -/GAGAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093330 | AGAGAAGAAAAAGAA[-/GAGAA]ACTAGAAACAGTTAA | 672 |
rs80357540 | in-del | -/TC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092787 | CAAGGAAAGAATGAG[-/TC]TAATATCAAGCCTGT | 672 |
rs80357541 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092872 | TGTGCAACATTCTCT[-/A]GCCCACTCTGGGTCC | 672 |
rs80357542 | in-del | -/CT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074380 | AACAGCTGGAAGAGT[-/CT]GGGCCACACGATTTG | 672 |
rs80357543 | in-del | -/GT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094204 | GAGGCTTTAATATGT[-/GT]AAAAGTGAAAGAGTT | 672 |
rs80357544 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104242 | AAACAGCTATAATTT[-/T]GCAAAAAAGGAAAAT | 672 |
rs80357545 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091749 | CAGAGGAGAATTTAT[-/T]ATCATTGAAGAATAG | 672 |
rs80357546 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093140 | GGAAGGCAAAAACAG[-/AA]CCAAATAAATGTGTG | 672 |
rs80357547 | in-del | -/TGAGA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092477 | AATGGGAAATGAGAA[-/TGAGA]CATTCCAAGTACAGT | 672 |
rs80357548 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082412 | CAGAACAAAGCACAT[-/T]CAGAAAAAGGTGTGT | 672 |
rs80357549 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092840 | AAAGAAACAAAGTCC[-/A]AAAAGTCACTTTTGA | 672 |
rs80357550 | in-del | -/GA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106501 | TTCTCAACCAGAAGA[-/GA]AAGGGCCTTCACAGT | 672 |
rs80357551 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099829 | GGAACTGTGAGAACT[-/C]TGAGGACAAAGCAGC | 672 |
rs80357552 | in-del | -/AATATACC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091818 | TTTGGTAAAGTAAAC[-/AATATACC]TTCTCAGTCTACTAG | 672 |
rs80357553 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063920 | TGAACGGACACTGAA[-/A]TATTTTCTAGGAATT | 672 |
rs80357554 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093457 | CAGACAAGTAAAAGA[-/C]ATGACAGCGATACTT | 672 |
rs80357555 | in-del | -/CAACA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094578 | GGCTTAGCAAGGAGC[-/CAACA]TAACAGATGGGCTGG | 672 |
rs80357556 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082471 | TTCTAACAGCTACCC[-/C]TTCCATCATAAGTGA | 672 |
rs80357557 | in-del | -/TA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093274 | AAAGATCTCATGTTA[-/TA]AGTGGAGAAAGGGTT | 672 |
rs80357558 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047693 | TCCAGGGTGTCCACC[-/C]AATTGTGGTTGTGCA | 672 |
rs80357559 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092644 | TTCAGAGGCAACGAA[-/A]CTGGACTCATTACTC | 672 |
rs80357560 | in-del | -/AAAAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091660 | CCTTAGTGAGGAAAC[-/AAAAT]GTTCTGCTAGCTTGT | 672 |
rs80357561 | in-del | -/ACTT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074348 | TGACGGAAACATCTT[-/ACTT]GCCAAGGCAAGATCT | 672 |
rs80357562 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091937 | CACCCATACACATTT[-/TT]GGCTCAGGGTTACCG | 672 |
rs80357564 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091821 | GTAAAGTAAACAATA[-/T]ACCTTCTCAGTCTAC | 672 |
rs80357565 | in-del | -/TC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090967 | CTCAGGGCTATCCTC[-/TC]AGAGTGACATTTTAA | 672 |
rs80357566 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093342 | GCCTTCCAAGAGAAG[-/G]AAAAAGAAGAGAAAC | 672 |
rs80357567 | in-del | -/CAGT | 1.64895e-05 | 0.00287132 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43093647 | GCTTGAACTAGTAGT[-/CAGT]AGAAATCTAAGCCCA | 672 |
rs80357568 | in-del | -/GT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104164 | TGGGCTACAGAAACC[-/GT]GCCAAAAGACTTCTA | 672 |
rs80357569 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094514 | CAGCACAGAAAAAAA[-/A]GGTAGATCTGAATGC | 672 |
rs80357570 | in-del | -/AT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094207 | TCATGAGGCTTTAAT[-/AT]GTAAAAGTGAAAGAG | 672 |
rs80357571 | in-del | -/T | 1.65194e-05 | 0.00287392 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43091905 | GAGGGGCCAAGAAAT[-/T]AGAGTCCTCAGAAGA | 672 |
rs80357572 | in-del | -/AG | 2.11889e-05 | 0.00325484 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43090963 | GGGCTATCCTCTCAG[-/AG]TGACATTTTAACCAC | 672 |
rs80357573 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092616 | CTCCAAATAAACATG[-/G]ACTTTTACAAAACCC | 672 |
rs80357574 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093317 | GAAACTAGAAACAGT[-/T]AAAGTGTCTAATAAT | 672 |
rs80357575 | in-del | -/AAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092202 | AGCATCCTGAAATAA[-/AAAA]GCAAGAATATGAAGA | 672 |
rs80357576 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094243 | TCTTCAGAGAAAATA[-/A]GACTTACTGGCCAGT | 672 |
rs80357577 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092133 | CTGATTTCAGATAAC[-/TT]AGAACAGCCTATGGG | 672 |
rs80357578 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091795 | TCTACTAGGCATAGC[-/A]CCGTTGCTACCGAGT | 672 |
rs80357579 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091761 | CTGTCTAAGAACACA[-/GA]GGAGAATTTATTATC | 672 |
rs80357580 | in-del | -/TAAC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067652 | AACACCACATCACTT[-/TAAC]TAATCTAATTACTGA | 672 |
rs80357581 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051087 | GAAATCTGTTGCTAT[-/G]GGCCCTTCACCAACA | 672 |
rs80357582 | in-del | -/C | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045778 | AGATGTGTGAGGCAC[-/C]TGTGGTGACCCGAGA | 672 |
rs80357583 | in-del | -/G | 3.29527e-05 | 0.00405898 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43093262 | TTAAGTGGAGAAAGG[-/G]TTTTGCAAACTGAAA | 672 |
rs80357584 | in-del | -/CA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091689 | TTGGCAAAGGCATCT[-/CA]GGAACATCACCTTAG | 672 |
rs80357585 | in-del | -/AAAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093707 | TTCAAAAGCACCTAA[-/AAAG]AATAGGCTGAGGAGG | 672 |
rs80357587 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094649 | TTTATTACTCACTAA[-/A]GACAGAATGAATGTA | 672 |
rs80357589 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091901 | GGGCCAAGAAATTAG[-/AG]TCCTCAGAAGAGAAC | 672 |
rs80357590 | in-del | -/C | 1.6528e-05 | 0.00287467 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43049192 | ATGTCCATTTTAGAT[-/C]AACTGGAATGGATGG | 672 |
rs80357591 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106489 | AGAAAGGGCCTTCAC[-/A]GTGTCCTTTATGTAA | 672 |
rs80357592 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094138 | ATATTTGGGAAAACC[-/C]TATCGGAAGAAGGCA | 672 |
rs80357594 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092822 | AGTCACTTTTGAATG[-/T]GAACAAAAGGAAGAA | 672 |
rs80357595 | in-del | -/TA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093453 | CAAGTAAAAGACATG[-/TA]ACAGCGATACTTTCC | 672 |
rs80357596 | in-del | -/GAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092849 | CTCTGGGTCCTTAAA[-/GAAA]CAAAGTCCAAAAGTC | 672 |
rs80357597 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094190 | TAAAAGTGAAAGAGT[-/G]TCACTCCAAATCAGT | 672 |
rs80357598 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093088 | AACCCCAAGGGACTA[-/A]TTCATGGTTGTTCCA | 672 |
rs80357599 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094068 | TAGGAGCATTTGTTA[-/A]CTGAGCCACAGATAA | 672 |
rs80357600 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093857 | TGAGAATAAAACAAA[-/A]GGTGATTCTATTCAG | 672 |
rs80357601 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092529 | AAAATCTGCTAGAGG[-/A]AAACTTTGAGGAACA | 672 |
rs80357602 | in-del | -/GT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093277 | CCCCAAAGATCTCAT[-/GT]TAAGTGGAGAAAGGG | 672 |
rs80357603 | in-del | -/GTCA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092926 | TCAAAGCGCCAGTCA[-/GTCA]TTTGCTCCGTTTTCA | 672 |
rs80357604 | in-del | -/A | 1.64928e-05 | 0.00287161 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43104233 | TAATTTTGCAAAAAA[-/A]GGAAAATAACTCTCC | 672 |
rs80357605 | in-del | -/TCAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092801 | ACAAAAGGAAGAAAA[-/TCAA]GGAAAGAATGAGTCT | 672 |
rs80357607 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093016 | GGACATGAAGTTAAC[-/C]ACAGTCGGGAAACAA | 672 |
rs80357608 | in-del | -/TG | 1.65996e-05 | 0.00288089 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43063923 | TGTGTGAACGGACAC[-/TG]AAATATTTTCTAGGA | 672 |
rs80357609 | in-del | -/GTAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091827 | TTGTTATTTGGTAAA[-/GTAAA]CAATATACCTTCTCA | 672 |
rs80357610 | in-del | -/CA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094550 | CTGGAAGTAAGGAAA[-/CA]TGTAATGATAGGCGG | 672 |
rs80357611 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092610 | AATAAACATGGACTT[-/TT]ACAAAACCCATATCG | 672 |
rs80357612 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094410 | ATGTTCCTTGGATAA[-/C]ACTAAATAGCAGCAT | 672 |
rs80357613 | in-del | -/ACTCCTG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093943 | TTGGCAGTTCAAAAG[-/ACTCCTG]AAATGATAAATCAGG | 672 |
rs80357614 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092805 | AACAAAAGGAAGAAA[-/A]TCAAGGAAAGAATGA | 672 |
rs80357615 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071070 | CTGCCCAGAGTCCAG[-/G]CTGCTGCTCATACTA | 672 |
rs80357616 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091710 | ACTGCAGTAACCAGG[-/G]TAATATTGGCAAAGG | 672 |
rs80357617 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092522 | TGCTAGAGGAAAACT[-/TT]GAGGAACATTCAATG | 672 |
rs80357618 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094515 | CCAGCACAGAAAAAA[-/A]GGTAGATCTGAATGC | 672 |
rs80357619 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093882 | TGATGAATATTACTA[-/A]TAGTGGTCATGAGAA | 672 |
rs80357620 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076508 | TTCTACCAGTAAAAA[-/A]TAAAGAACCAGGAGT | 672 |
rs80357621 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092000 | AAGTTCTGCTGTTTT[-/T]AGCAAAAGCGTCCAG | 672 |
rs80357622 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094620 | TAGAAAAGGCTGAAT[-/T]CTGTAATAAAAGCAA | 672 |
rs80357623 | in-del | -/CTAAT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067643 | ATCACTTTAACTAAT[-/CTAAT]TACTGAAGAGACTAC | 672 |
rs80357624 | in-del | -/A/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092275 | AATGCTATGCTTAGA[-/A/GA]TTAGGGGTTTTGCAA | 672 |
rs80357625 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092276 | GAATGCTATGCTTAG[-/A]ATTAGGGGTTTTGCA | 672 |
rs80357626 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093512 | CATGGAAGGTAAAGA[-/A]CCTGCAACTGGAGCC | 672 |
rs80357627 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092579 | TATACCACCACTTTT[-/T]CCCATCAAGTCATTT | 672 |
rs80357628 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094756 | GCTGAGAGGCATCCA[-/G]AAAAGTATCAGGGTA | 672 |
rs80357629 | in-del | -/A | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045711 | GGAGCTGGACACCTA[-/A]CCTGATACCCCAGAT | 672 |
rs80357630 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093980 | TCATCCTGAGGATTT[-/T]ATCAAGAAAGCAGAT | 672 |
rs80357631 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093055 | GATAATAGAAATGAC[-/A]CAGAAGGCTTTAAGT | 672 |
rs80357632 | in-del | -/AAAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094031 | AGAGCGTCCCCTCAC[-/AAAT]AAATTAAAGCGTAAA | 672 |
rs80357633 | in-del | -/CC | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124023 | AAAATCTTAGAGTGT[-/CC]CATCTGGTAAGTCAG | 672 |
rs80357634 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091622 | ACAGTGCAGTGAATT[-/T]GGAAGACTTGACTGC | 672 |
rs80357635 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092302 | ACTAGGTAGAAACAG[-/AG]GGCCAAAATTGAATG | 672 |
rs80357636 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092845 | GTCCTTAAAGAAACA[-/AA]GTCCAAAAGTCACTT | 672 |
rs80357637 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106525 | TTTATAGATTTTGCA[-/T]GCTGAAACTTCTCAA | 672 |
rs80357638 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093514 | CTCATGGAAGGTAAA[-/G]AACCTGCAACTGGAG | 672 |
rs80357639 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099802 | CAGCGGATACAACCT[-/C]AAAAGACGTCTGTCT | 672 |
rs80357640 | in-del | -/AGAAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093814 | AAATCCTAACCCAAT[-/AGAAT]CACTCGAAAAAGAAT | 672 |
rs80357641 | in-del | -/AG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071164 | TCCTTCTGAAGACAG[-/AG]CCCCAGAGTCAGCTC | 672 |
rs80357642 | in-del | -/TT | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124031 | TATGCAGAAAATCTT[-/TT]AGAGTGTCCCATCTG | 672 |
rs80357643 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093570 | GAGATAAAGAAAAAA[-/AA]GTACAACCAAATGCC | 672 |
rs80357644 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094608 | GAATTCTGTAATAAA[-/AG]CAAACAGCCTGGCTT | 672 |
rs80357645 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091769 | CCGAGTGTCTGTCTA[-/AG]AACACAGAGGAGAAT | 672 |
rs80357646 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091629 | TTTTCTTCACAGTGC[-/AG]TGAATTGGAAGACTT | 672 |
rs80357647 | in-del | -/TAATAACATTA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092437 | GAGCACAATTAGCCG[-/TAATAACATTA]GAGAAAATGTTTTTA | 672 |
rs80357648 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094087 | GTAACTGAAAATCTA[-/A]TTATAGGAGCATTTG | 672 |
rs80357649 | in-del | -/AC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082565 | TTGAAGCAGAGGGAT[-/AC]CATGCAACATAACCT | 672 |
rs80357650 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093290 | TAATGCTGAAGACCC[-/C]AAAGATCTCATGTTA | 672 |
rs80357652 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093694 | AAGAATAGGCTGAGG[-/A]GGAAGTCTTCTACCA | 672 |
rs80357653 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070980 | CAGCTTCAACAGAAA[-/G]GGTCAACAAAAGAAT | 672 |
rs80357654 | in-del | -/CA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093320 | AAGAGAAACTAGAAA[-/CA]GTTAAAGTGTCTAAT | 672 |
rs80357655 | in-del | -/AA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070969 | AGAAAGGGTCAACAA[-/AA]GAATGTCCATGGTGG | 672 |
rs80357656 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071022 | ATGCAATGGAAGAAA[-/A]GTGTGAGCAGGGAGA | 672 |
rs80357657 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093247 | GGTTTTGCAAACTGA[-/AA]GATCTGTAGAGAGTA | 672 |
rs80357658 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093044 | TGACACAGAAGGCTT[-/T]AAGTATCCATTGGGA | 672 |
rs80357659 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092861 | CTCTGCCCACTCTGG[-/G]TCCTTAAAGAAACAA | 672 |
rs80357660 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106497 | CAACCAGAAGAAAGG[-/G]CCTTCACAGTGTCCT | 672 |
rs80357661 | in-del | -/GTTA | 1.64773e-05 | 0.00287026 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43092761 | AAGCCTGTACAGACA[-/GTTA]ATATCACTGCAGGCT | 672 |
rs80357662 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093975 | CTGAGGATTTTATCA[-/A]GAAAGCAGATTTGGC | 672 |
rs80357663 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091951 | AGTCCTAGCCCTTTC[-/A]CCCATACACATTTGG | 672 |
rs80357664 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093119 | ATAAATGTGTGAGTC[-/AG]TGTGCAGCATTTGAA | 672 |
rs80357665 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094429 | AATCCTAGAGATACT[-/C]GAAGATGTTCCTTGG | 672 |
rs80357666 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091824 | TTTGGTAAAGTAAAC[-/AA]TATACCTTCTCAGTC | 672 |
rs80357668 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093355 | TTTGTCAATCCTAGC[-/C]TTCCAAGAGAAGAAA | 672 |
rs80357669 | in-del | -/C | 3.30603e-05 | 0.0040656 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43093074 | AATTCATGGTTGTTC[-/C]AAAGATAATAGAAAT | 672 |
rs80357670 | in-del | -/GT | 1.6477e-05 | 0.00287024 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43094635 | AAAGACAGAATGAAT[-/GT]AGAAAAGGCTGAATT | 672 |
rs80357671 | in-del | -/TTCC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091852 | GAAGAGCTTCCCTGC[-/TTCC]AACACTTGTTATTTG | 672 |
rs80357672 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067610 | ATGTTGTTATGAAAA[-/A]CAGGTATACCAAGAA | 672 |
rs80357673 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067642 | TTTAACTAATCTAAT[-/T]ACTGAAGAGACTACT | 672 |
rs80357674 | in-del | -/GAGT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093122 | ACCAAATAAATGTGT[-/GAGT]CAGTGTGCAGCATTT | 672 |
rs80357675 | in-del | -/GGTTTCAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092938 | GCAGAATACATTCAA[-/GGTTTCAA]AGCGCCAGTCATTTG | 672 |
rs80357676 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057086 | GAAGAAACCACCAAG[-/G]TCCAAAGCGAGCAAG | 672 |
rs80357678 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091614 | AGTGAATTGGAAGAC[-/TT]GACTGCAAATACAAA | 672 |
rs80357679 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093081 | AGGGACTAATTCATG[-/G]TTGTTCCAAAGATAA | 672 |
rs80357680 | in-del | -/AAAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092202 | AAGCATCCTGAAATA[-/AAAAA]GCAAGAATATGAAGA | 672 |
rs80357681 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093257 | TGGAGAAAGGGTTTT[-/T]GCAAACTGAAAGATC | 672 |
rs80357682 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106524 | TTATAGATTTTGCAT[-/G]CTGAAACTTCTCAAC | 672 |
rs80357683 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094212 | ATCCTCATGAGGCTT[-/T]AATATGTAAAAGTGA | 672 |
rs80357684 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051111 | TTCTTCCAGATCTTC[-/A]GGGGGCTAGAAATCT | 672 |
rs80357685 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092804 | ACAAAAGGAAGAAAA[-/A]TCAAGGAAAGAATGA | 672 |
rs80357686 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092242 | TGAGGTCTATAAACA[-/AA]GTCTTCCTGGAAGTA | 672 |
rs80357687 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091771 | ACCGAGTGTCTGTCT[-/T]AAGAACACAGAGGAG | 672 |
rs80357688 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093460 | GAACAGACAAGTAAA[-/A]GACATGACAGCGATA | 672 |
rs80357689 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094601 | TAATAAAAGCAAACA[-/G]CCTGGCTTAGCAAGG | 672 |
rs80357690 | in-del | -/TG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094577 | AGCAAGGAGCCAACA[-/TG]TAACAGATGGGCTGG | 672 |
rs80357691 | in-del | -/TG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091006 | ATCTGGGTGTGAGAG[-/TG]AAACAAGCGTCTCTG | 672 |
rs80357692 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092201 | TCCTGAAATAAAAAA[-/A]GCAAGAATATGAAGA | 672 |
rs80357693 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092659 | TGTCTATCATCTCAG[-/A]TTCAGAGGCAACGAA | 672 |
rs80357694 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049186 | ATTTTAGATCAACTG[-/G]AATGGATGGTACAGC | 672 |
rs80357695 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093141 | GGGAAGGCAAAAACA[-/GA]ACCAAATAAATGTGT | 672 |
rs80357696 | in-del | -/GTGTCCCATCT | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124018 | GCAGAAAATCTTAGA[-/GTGTCCCATCT]GGTAAGTCAGCACAA | 672 |
rs80357697 | in-del | -/AAAG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104942 | TCAGGAGCCTACAAG[-/AAAG]TACGAGATTTAGTCA | 672 |
rs80357698 | in-del | -/TAAC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093920 | GATAAATCAGGGAAC[-/TAAC]CAAACGGAGCAGAAT | 672 |
rs80357699 | in-del | -/CT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074410 | GCTCATTAAGGTTGT[-/CT]TGATGTGGAGGAGCA | 672 |
rs80357700 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094800 | ATCAACCCAGTAATA[-/A]TGATTTGAACACCAC | 672 |
rs80357701 | in-del | -/AGCA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092199 | ATCCTGAAATAAAAA[-/AGCA]AGAATATGAAGAAGT | 672 |
rs80357702 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092350 | TCCAGTATTAATGAA[-/A]TAGGTTCCAGTGATG | 672 |
rs80357703 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092769 | ATATCAAGCCTGTAC[-/A]GACAGTTAATATCAC | 672 |
rs80357704 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091764 | GTCTGTCTAAGAACA[-/A]CAGAGGAGAATTTAT | 672 |
rs80357705 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070978 | GCTTCAACAGAAAGG[-/G]TCAACAAAAGAATGT | 672 |
rs80357706 | in-del | -/TG | 1.64819e-05 | 0.00287066 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43093125 | AACCAAATAAATGTG[-/TG]AGTCAGTGTGCAGCA | 672 |
rs80357707 | in-del | -/GTTC | 1.65418e-05 | 0.00287587 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43094737 | AAAAGTATCAGGGTA[-/GTTC]TGTTTCAAACTTGCA | 672 |
rs80357708 | in-del | -/TG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099836 | CTAACCTTGGAACTG[-/TG]AGAACTCTGAGGACA | 672 |
rs80357709 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104156 | GAAACCGTGCCAAAA[-/A]GACTTCTACAGAGTG | 672 |
rs80357710 | in-del | -/TG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063934 | TGCTGAGTTTGTGTG[-/TG]AACGGACACTGAAAT | 672 |
rs80357711 | in-del | -/A | 8.23934e-05 | 0.00641794 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43091496 | GGTTTCAGATGATGA[-/A]GAAAGAGGAACGGGC | 672 |
rs80357712 | in-del | -/AAATC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092803 | TGAACAAAAGGAAGA[-/AAATC]AAGGAAAGAATGAGT | 672 |
rs80357713 | in-del | -/AG | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124030 | TATGCAGAAAATCTT[-/AG]AGTGTCCCATCTGGT | 672 |
rs80357714 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094150 | ATTGAAGACAAAATA[-/A]TTTGGGAAAACCTAT | 672 |
rs80357715 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093375 | ATACCAGTGAACTTA[-/A]AAGAATTTGTCAATC | 672 |
rs80357716 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082475 | AGCCTTCTAACAGCT[-/G]ACCCTTCCATCATAA | 672 |
rs80357717 | in-del | -/AT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092823 | AAGTCACTTTTGAAT[-/AT]GTGAACAAAAGGAAG | 672 |
rs80357718 | in-del | -/TCTCT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071198 | CTGGAATCAGCCTCT[-/TCTCT]GATGACCCTGAATCT | 672 |
rs80357719 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094679 | ATGCCAGCTCATTAC[-/AG]CATGAGAACAGCAGT | 672 |
rs80357720 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063876 | GGGTAGTTAGCTATT[-/T]CTGTAAGTATAATAC | 672 |
rs80357721 | in-del | -/A | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045749 | GAGTGGGTGTTGGAC[-/A]GTGTAGCACTCTACC | 672 |
rs80357722 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094145 | AGACAAAATATTTGG[-/G]AAAACCTATCGGAAG | 672 |
rs80357723 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093774 | AAACGAAAGCTGAAC[-/C]TATAAGCAGCAGTAT | 672 |
rs80357724 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094732 | TCAGGGTAGTTCTGT[-/TT]CAAACTTGCATGTGG | 672 |
rs80357725 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093202 | GTACCTGGTACTGAT[-/T]ATGGCACTCAGGAAA | 672 |
rs80357726 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094628 | AATGAATGTAGAAAA[-/T]GGCTGAATTCTGTAA | 672 |
rs80357727 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091489 | AGATGATGAAGAAAG[-/AG]GAACGGGCTTGGAAG | 672 |
rs80357728 | in-del | -/TG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115776 | CCTACCCTGCTAGTC[-/TG]GAGTTGATCAAGGAA | 672 |
rs80357729 | in-del | -/A | 1.65181e-05 | 0.00287381 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43091903 | GGGGCCAAGAAATTA[-/A]GAGTCCTCAGAAGAG | 672 |
rs80357730 | in-del | -/GA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063348 | AGTCTATTAAAGAAA[-/GA]AAAATGCTGAATGAG | 672 |
rs80357731 | in-del | -/GAAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092809 | GAATGTGAACAAAAG[-/GAAG]AAAATCAAGGAAAGA | 672 |
rs80357732 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057055 | AGAATCCCAGGACAG[-/A]AAGGTAAAGCTCCCT | 672 |
rs80357733 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093463 | AATGAACAGACAAGT[-/A]AAAGACATGACAGCG | 672 |
rs80357734 | in-del | -/T | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106528 | TAATTTATAGATTTT[-/T]GCATGCTGAAACTTC | 672 |
rs80357735 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094001 | AAGGAGACCTACATC[-/A]GGCCTTCATCCTGAG | 672 |
rs80357736 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093706 | AAAGCACCTAAAAAG[-/A]ATAGGCTGAGGAGGA | 672 |
rs80357737 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091446 | AAGAGCAAAGCATGG[-/A]TTCAAACTTAGGTAT | 672 |
rs80357738 | in-del | -/CA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104878 | CTTTTCAGCTTGACA[-/CA]GGTTTGGAGTGTAAG | 672 |
rs80357739 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093171 | GTATCTCGTTACTGG[-/G]AAGTTAGCACTCTAG | 672 |
rs80357740 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093054 | ATAATAGAAATGACA[-/C]AGAAGGCTTTAAGTA | 672 |
rs80357741 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092597 | TTTACAAAACCCATA[-/T]CGTATACCACCACTT | 672 |
rs80357742 | in-del | -/TC | 2.35369e-05 | 0.00343044 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43090945 | ACATTTTAACCACTC[-/TC]AGGTAAAAAGCGTGT | 672 |
rs80357743 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063371 | ATGATCTCTTTAGGG[-/G]TGACCCAGTCTATTA | 672 |
rs80357744 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049174 | CTGGAATGGATGGTA[-/A]CAGCTGTGTGGTGCT | 672 |
rs80357745 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095848 | TGGATTCTGCAAAAA[-/A]GGGTAATGGCAAAGT | 672 |
rs80357746 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092486 | TGAAAGAGAAATGGG[-/G]AAATGAGAACATTCC | 672 |
rs80357747 | in-del | -/GT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094833 | TTTTCTGAGACGGAT[-/GT]AACAAATACTGAACA | 672 |
rs80357748 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082439 | CTTCTGCCCTTGAGG[-/G]ACCTGCGAAATCCAG | 672 |
rs80357749 | in-del | -/TTCA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092510 | AAACTTTGAGGAACA[-/TTCA]ATGTCACCTGAAAGA | 672 |
rs80357750 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115759 | AGTTGATCAAGGAAC[-/C]TGTCTCCACAAAGTG | 672 |
rs80357751 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051066 | TTCACCAACATGCCC[-/C]ACAGGTAAGAGCCTG | 672 |
rs80357753 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093577 | AGTGAAGAGATAAAG[-/G]AAAAAAAAGTACAAC | 672 |
rs80357754 | in-del | -/AG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104233 | ATAATTTTGCAAAAA[-/AG]GAAAATAACTCTCCT | 672 |
rs80357755 | in-del | -/GAAGA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093333 | CCAAGAGAAGAAAAA[-/GAAGA]GAAACTAGAAACAGT | 672 |
rs80357756 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092939 | TACATTCAAGGTTTC[-/A]AAGCGCCAGTCATTT | 672 |
rs80357757 | in-del | -/GA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045790 | CAGCAATTGGGCAGA[-/GA]TGTGTGAGGCACCTG | 672 |
rs80357758 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099793 | CAACCTCAAAAGACG[-/T]CTGTCTACATTGAAT | 672 |
rs80357759 | in-del | -/TG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094636 | TAAAGACAGAATGAA[-/TG]TAGAAAAGGCTGAAT | 672 |
rs80357760 | in-del | -/TT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063941 | CTGCAGATGCTGAGT[-/TT]GTGTGTGAACGGACA | 672 |
rs80357761 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070972 | ACAGAAAGGGTCAAC[-/A]AAAGAATGTCCATGG | 672 |
rs80357762 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099827 | AACTGTGAGAACTCT[-/T]GAGGACAAAGCAGCG | 672 |
rs80357763 | in-del | -/AAAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092208 | ATTGTAAGCATCCTG[-/AAAT]AAAAAAGCAAGAATA | 672 |
rs80357764 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092274 | ATGCTATGCTTAGAT[-/GA]TAGGGGTTTTGCAAC | 672 |
rs80357765 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082551 | ACCATGCAACATAAC[-/C]TGATAAAGCTCCAGC | 672 |
rs80357766 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094255 | GAATATTCTGGTTCT[-/T]CAGAGAAAATAGACT | 672 |
rs80357767 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091737 | TATTATCATTGAAGA[-/A]TAGCTTAAATGACTG | 672 |
rs80357768 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093637 | GTCAGTAGAAATCTA[-/T]AGCCCACCTAATTGT | 672 |
rs80357769 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092372 | TTCCAGTACTAATGA[-/G]AGTGGGCTCCAGTAT | 672 |
rs80357770 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094141 | AAAATATTTGGGAAA[-/A]CCTATCGGAAGAAGG | 672 |
rs80357771 | in-del | -/AAGAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093332 | CAAGAGAAGAAAAAG[-/AAGAG]AAACTAGAAACAGTT | 672 |
rs80357772 | in-del | -/AT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094549 | TGGAAGTAAGGAAAC[-/AT]GTAATGATAGGCGGA | 672 |
rs80357773 | in-del | -/CA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093451 | AAGTAAAAGACATGA[-/CA]GCGATACTTTCCCAG | 672 |
rs80357774 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094513 | AGCACAGAAAAAAAG[-/G]TAGATCTGAATGCTG | 672 |
rs80357775 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094546 | AGTAAGGAAACATGT[-/C]AATGATAGGCGGACT | 672 |
rs80357776 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094401 | GGATAACACTAAATA[-/A]GCAGCATTCAGAAAG | 672 |
rs80357777 | in-del | -/AAGC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092200 | CATCCTGAAATAAAA[-/AAGC]AAGAATATGAAGAAG | 672 |
rs80357778 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094090 | CATGTAACTGAAAAT[-/A]CTAATTATAGGAGCA | 672 |
rs80357779 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091478 | AAGAGGAACGGGCTT[-/T]GGAAGAAAATAATCA | 672 |
rs80357780 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093234 | GAAAGATCTGTAGAG[-/AG]TAGCAGTATTTCATT | 672 |
rs80357781 | in-del | -/AAAG | 1.64849e-05 | 0.00287092 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43092051 | AGATGATGGTGAAAT[-/AAAG]GAAGATACTAGTTTT | 672 |
rs80357782 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094008 | AGCGTAAAAGGAGAC[-/C]TACATCAGGCCTTCA | 672 |
rs80357784 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093830 | TCAGAATGAGAAAAA[-/A]TCCTAACCCAATAGA | 672 |
rs80357785 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092179 | TATGAAGAAGTAGTT[-/T]CAGACTGTTAATACA | 672 |
rs80357786 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093232 | AGATCTGTAGAGAGT[-/A]GCAGTATTTCATTGG | 672 |
rs80357787 | in-del | -/AG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091008 | GCATCTGGGTGTGAG[-/AG]TGAAACAAGCGTCTC | 672 |
rs80357788 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090965 | AGGGCTATCCTCTCA[-/A]GAGTGACATTTTAAC | 672 |
rs80357789 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094733 | ATCAGGGTAGTTCTG[-/TT]TCAAACTTGCATGTG | 672 |
rs80357790 | in-del | -/A | 1.64732e-05 | 0.0028699 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43082460 | ACCCTTCCATCATAA[-/A]GTGACTCTTCTGCCC | 672 |
rs80357791 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057088 | TGGAAGAAACCACCA[-/A]GGTCCAAAGCGAGCA | 672 |
rs80357792 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094688 | AAATACTCATGCCAG[-/AG]CTCATTACAGCATGA | 672 |
rs80357793 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093321 | AAGAGAAACTAGAAA[-/C]AGTTAAAGTGTCTAA | 672 |
rs80357794 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094234 | AAAATAGACTTACTG[-/G]CCAGTGATCCTCATG | 672 |
rs80357795 | in-del | -/TC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071149 | AGCCCCAGAGTCAGC[-/TC]GTGTTGGCAACATAC | 672 |
rs80357796 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094464 | AAGAATGGAATAAGC[-/A]GAAACTGCCATGCTC | 672 |
rs80357797 | in-del | -/NNNN/TTCC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091859 | GGATGAAGAGCTTCC[-/NNNN/TTCC]CTGCTTCCAACACTT | 672 |
rs80357798 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091754 | GAACACAGAGGAGAA[-/T]TTATTATCATTGAAG | 672 |
rs80357799 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093063 | GTTCCAAAGATAATA[-/G]AAATGACACAGAAGG | 672 |
rs80357800 | in-del | -/CA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093053 | ATAATAGAAATGACA[-/CA]GAAGGCTTTAAGTAT | 672 |
rs80357801 | in-del | -/ATTA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094084 | GTAACTGAAAATCTA[-/ATTA]TAGGAGCATTTGTTA | 672 |
rs80357802 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093313 | CTAGAAACAGTTAAA[-/A]GTGTCTAATAATGCT | 672 |
rs80357803 | in-del | -/T | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124033 | GCTATGCAGAAAATC[-/T]TAGAGTGTCCCATCT | 672 |
rs80357804 | in-del | -/TG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091012 | AGCAGCATCTGGGTG[-/TG]AGAGTGAAACAAGCG | 672 |
rs80357805 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091888 | AGAGTCCTCAGAAGA[-/GA]ACTTATCTAGTGAGG | 672 |
rs80357806 | in-del | -/AATG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094635 | AAGACAGAATGAATG[-/AATG]TAGAAAAGGCTGAAT | 672 |
rs80357808 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092089 | TCTCAGGTTTGTTCT[-/G]AGACACCTGATGACC | 672 |
rs80357809 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094265 | TGAGGTAGATGAATA[-/A]TTCTGGTTCTTCAGA | 672 |
rs80357810 | in-del | -/GG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091759 | GTCTAAGAACACAGA[-/GG]AGAATTTATTATCAT | 672 |
rs80357811 | in-del | -/C | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124064 | TCGCGTTGAAGAAGT[-/C]ACAAAATGTCATTAA | 672 |
rs80357812 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092765 | CAAGCCTGTACAGAC[-/A]GTTAATATCACTGCA | 672 |
rs80357813 | in-del | -/AA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074431 | GAAACTACCCATCTC[-/AA]GAGGAGCTCATTAAG | 672 |
rs80357814 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093420 | GAGCTGAAGTTAACA[-/AA]TGCACCTGGTTCTTT | 672 |
rs80357815 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092235 | ATAAACAAAGTCTTC[-/C]TGGAAGTAATTGTAA | 672 |
rs80357816 | in-del | -/CTACAGA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104145 | CGTGCCAAAAGACTT[-/CTACAGA]GTGAACCCGAAAATC | 672 |
rs80357817 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094019 | AAATAAATTAAAGCG[-/G]TAAAAGGAGACCTAC | 672 |
rs80357818 | in-del | -/AA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051074 | TATGGGCCCTTCACC[-/AA]CATGCCCACAGGTAA | 672 |
rs80357819 | in-del | -/TCATC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092664 | TCTAGGTTTTGTCTA[-/TCATC]TCAGTTCAGAGGCAA | 672 |
rs80357820 | in-del | -/CGTTACT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093174 | CTCAGGAAAGTATCT[-/CGTTACT]GGAAGTTAGCACTCT | 672 |
rs80357821 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094404 | CTTGGATAACACTAA[-/A]TAGCAGCATTCAGAA | 672 |
rs80357822 | in-del | -/ACAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092764 | ATCAAGCCTGTACAG[-/ACAG]TTAATATCACTGCAG | 672 |
rs80357823 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051075 | TATGGGCCCTTCACC[-/C]AACATGCCCACAGGT | 672 |
rs80357824 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094846 | GCTGCTTGTGAATTT[-/T]CTGAGACGGATGTAA | 672 |
rs80357825 | in-del | -/ATCCAGAA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082423 | TTGAGGACCTGCGAA[-/ATCCAGAA]CAAAGCACATCAGAA | 672 |
rs80357826 | in-del | -/TC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074411 | AGCTCATTAAGGTTG[-/TC]TTGATGTGGAGGAGC | 672 |
rs80357827 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092174 | AGAAGTAGTTCAGAC[-/T]GTTAATACAGATTTC | 672 |
rs80357828 | in-del | -/TC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092155 | TAATACAGATTTCTC[-/TC]CATATCTGATTTCAG | 672 |
rs80357829 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092540 | TAAATGTAAGAAAAA[-/AA]TCTGCTAGAGGAAAA | 672 |
rs80357830 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093056 | AGATAATAGAAATGA[-/A]CACAGAAGGCTTTAA | 672 |
rs80357831 | in-del | -/A/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091881 | CAGAAGAGAACTTAT[-/A/T]CTAGTGAGGATGAAG | 672 |
rs80357832 | in-del | -/GATA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092722 | GTGGTTGGTCAGAAA[-/GATA]AGCCAGTTGATAATG | 672 |
rs80357833 | in-del | -/AA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070980 | CAGCTTCAACAGAAA[-/AA]GGGTCAACAAAAGAA | 672 |
rs80357834 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093801 | GAATCACTCGAAAAA[-/GA]ATCTGCTTTCAAAAC | 672 |
rs80357835 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092973 | AAGAAAGTGAACTTG[-/A]ATGCTCAGTATTTGC | 672 |
rs80357836 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094459 | TGGAATAAGCAGAAA[-/C]TGCCATGCTCAGAGA | 672 |
rs80357837 | in-del | -/CA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071159 | CTGAAGACAGAGCCC[-/CA]GAGTCAGCTCGTGTT | 672 |
rs80357838 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049143 | CTGTGGTGAAGGAGC[-/T]TTTCATCATTCACCC | 672 |
rs80357839 | in-del | -/G | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045760 | TGGTGACCCGAGAGT[-/G]GGTGTTGGACAGTGT | 672 |
rs80357840 | in-del | -/TGGT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092732 | AGGCTTTCCTGTGGT[-/TGGT]CAGAAAGATAAGCCA | 672 |
rs80357841 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092423 | TAGAGAAAATGTTTT[-/T]AAAGAAGCCAGCTCA | 672 |
rs80357842 | in-del | -/AGTG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091672 | CAGGAACATCACCTT[-/AGTG]AGGAAACAAAATGTT | 672 |
rs80357843 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092171 | AAGTAGTTCAGACTG[-/TT]AATACAGATTTCTCT | 672 |
rs80357844 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094602 | GTAATAAAAGCAAAC[-/A]GCCTGGCTTAGCAAG | 672 |
rs80357845 | in-del | -/CT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091961 | AGCTTAGCAGGAGTC[-/CT]AGCCCTTTCACCCAT | 672 |
rs80357846 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092526 | ATCTGCTAGAGGAAA[-/A]CTTTGAGGAACATTC | 672 |
rs80357847 | in-del | -/AG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090961 | CTATCCTCTCAGAGT[-/AG]GACATTTTAACCACT | 672 |
rs80357848 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091766 | GTGTCTGTCTAAGAA[-/A]CACAGAGGAGAATTT | 672 |
rs80357849 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091752 | ACACAGAGGAGAATT[-/A]TATTATCATTGAAGA | 672 |
rs80357850 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093138 | AGGCAAAAACAGAAC[-/C]AAATAAATGTGTGAG | 672 |
rs80357851 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093633 | GTAGAAATCTAAGCC[-/C]ACCTAATTGTACTGA | 672 |
rs80357852 | in-del | -/AA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057099 | AGATGTGGTCAATGG[-/AA]GAAACCACCAAGGTC | 672 |
rs80357853 | in-del | -/A | 1.6489e-05 | 0.00287128 | BRCA1 | 17 | allele_origin=A(germline,somatic)/+.-----(germline) | 17:43093569 | GATAAAGAAAAAAAA[-/A]GTACAACCAAATGCC | 672 |
rs80357854 | in-del | -/AA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076489 | AGAACCAGGAGTGGA[-/AA]GGTAAGAAACATCAA | 672 |
rs80357855 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091675 | CAGGAACATCACCTT[-/A]GTGAGGAAACAAAAT | 672 |
rs80357856 | in-del | -/NNNNN/TGAGA | 6.5937e-05 | 0.00574144 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline)/5(germline) | 17:43092478 | AAATGGGAAATGAGA[-/NNNNN/TGAGA]ACATTCCAAGTACAG | 672 |
rs80357857 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092068 | CCTGATGACCTGTTA[-/A]GATGATGGTGAAATA | 672 |
rs80357858 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092273 | TGCTATGCTTAGATT[-/T]AGGGGTTTTGCAACC | 672 |
rs80357859 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094327 | GACTCACATGATGGG[-/G]AGTCTGAATCAAATG | 672 |
rs80357860 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093325 | AAAGAAGAGAAACTA[-/G]AAACAGTTAAAGTGT | 672 |
rs80357861 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091016 | TGAAGCAGCATCTGG[-/G]TGTGAGAGTGAAACA | 672 |
rs80357862 | in-del | -/CTAA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067649 | ACCACATCACTTTAA[-/CTAA]TCTAATTACTGAAGA | 672 |
rs80357863 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093018 | TGGGACATGAAGTTA[-/A]CCACAGTCGGGAAAC | 672 |
rs80357864 | in-del | -/AACA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091597 | TTGACTGCAAATACA[-/AACA]CCCAGGATCCTTTCT | 672 |
rs80357865 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092169 | TAGTTCAGACTGTTA[-/A]TACAGATTTCTCTCC | 672 |
rs80357866 | in-del | -/TGAGA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092483 | AAGAGAAATGGGAAA[-/TGAGA]TGAGAACATTCCAAG | 672 |
rs80357867 | in-del | -/GAAA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063350 | ACCCAGTCTATTAAA[-/GAAA]GAAAAATGCTGAATG | 672 |
rs80357868 | in-del | -/GTCT | 4.94271e-05 | 0.00497102 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43091772 | TGCTACCGAGTGTCT[-/GTCT]AAGAACACAGAGGAG | 672 |
rs80357869 | in-del | -/G | | | frameshift-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43106473 | GTGTCCTTTATGTAA[-/G]AATGATATAACCAAA | 672 |
rs80357870 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063881 | AAAATGGGTAGTTAG[-/C]TATTTCTGTAAGTAT | 672 |
rs80357871 | in-del | -/A/NNN | | | frameshift-variant, cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093405 | ATGCACCTGGTTCTT[-/A/NNN]TTACTAAGTGTTCAA | 672 |
rs80357872 | in-del | -/C | 1.6473e-05 | 0.00286988 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43099808 | ACAAAGCAGCGGATA[-/C]AACCTCAAAAGACGT | 672 |
rs80357873 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091832 | CTTGTTATTTGGTAA[-/A]GTAAACAATATACCT | 672 |
rs80357874 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063900 | TTCTAGGAATTGCGG[-/G]AGGAAAATGGGTAGT | 672 |
rs80357876 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092591 | AAACCCATATCGTAT[-/A]CCACCACTTTTTCCC | 672 |
rs80357877 | in-del | -/GAAGATACTAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092040 | GATGGTGAAATAAAG[-/GAAGATACTAG]TTTTGCTGAAAATGA | 672 |
rs80357878 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091700 | CCAGGTAATATTGGC[-/C]AAAGGCATCTCAGGA | 672 |
rs80357879 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094148 | TGAAGACAAAATATT[-/T]GGGAAAACCTATCGG | 672 |
rs80357880 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093425 | CCCAGAGCTGAAGTT[-/T]AACAAATGCACCTGG | 672 |
rs80357881 | in-del | -/TC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104220 | AAAGGAAAATAACTC[-/TC]CTGAACATCTAAAAG | 672 |
rs80357882 | in-del | -/CA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099865 | GCAGGAAACCAGTCT[-/CA]GTGTCCAACTCTCTA | 672 |
rs80357883 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092336 | AATAGGTTCCAGTGA[-/G]TGAAAACATTCAAGC | 672 |
rs80357884 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104937 | CTACAAGAAAGTACG[-/A]GATTTAGTCAACTTG | 672 |
rs80357885 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093578 | CAGTGAAGAGATAAA[-/A]GAAAAAAAAGTACAA | 672 |
rs80357886 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051109 | CTTCCAGATCTTCAG[-/G]GGGGCTAGAAATCTG | 672 |
rs80357887 | in-del | -/CT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099851 | TCAGTGTCCAACTCT[-/CT]AACCTTGGAACTGTG | 672 |
rs80357888 | in-del | -/TTAAA | 3.30036e-05 | 0.0040621 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43094023 | CCCCTCACAAATAAA[-/TTAAA]GCGTAAAAGGAGACC | 672 |
rs80357889 | in-del | -/TGAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091670 | GGAACATCACCTTAG[-/TGAG]GAAACAAAATGTTCT | 672 |
rs80357890 | in-del | -/TG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092641 | CAGAGGCAACGAAAC[-/TG]GACTCATTACTCCAA | 672 |
rs80357891 | in-del | -/AAAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092852 | CCACTCTGGGTCCTT[-/AAAG]AAACAAAGTCCAAAA | 672 |
rs80357892 | in-del | -/CA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092165 | TTCAGACTGTTAATA[-/CA]GATTTCTCTCCATAT | 672 |
rs80357893 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092621 | CATTACTCCAAATAA[-/A]CATGGACTTTTACAA | 672 |
rs80357894 | in-del | -/TTAACTAATCT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067646 | AAACACCACATCACT[-/TTAACTAATCT]AATTACTGAAGAGAC | 672 |
rs80357895 | in-del | -/TG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063369 | TGATCTCTTTAGGGG[-/TG]ACCCAGTCTATTAAA | 672 |
rs80357896 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067647 | ATCACTTTAACTAAT[-/C]TAATTACTGAAGAGA | 672 |
rs80357897 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094444 | ACTGCCATGCTCAGA[-/GA]ATCCTAGAGATACTG | 672 |
rs80357899 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092830 | AAGTCCAAAAGTCAC[-/TT]TTGAATGTGAACAAA | 672 |
rs80357900 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092141 | TCCATATCTGATTTC[-/A]GATAACTTAGAACAG | 672 |
rs80357901 | in-del | -/T | 1.65151e-05 | 0.00287355 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43093759 | CTATAAGCAGCAGTA[-/T]AAGCAATATGGAACT | 672 |
rs80357902 | in-del | -/A | 1.64893e-05 | 0.0028713 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43091882 | TCAGAAGAGAACTTA[-/A]TCTAGTGAGGATGAA | 672 |
rs80357903 | in-del | -/CAAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092197 | CCTGAAATAAAAAAG[-/CAAG]AATATGAAGAAGTAG | 672 |
rs80357904 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091558 | TCTTCCAAACAAATG[-/A]GGCATCAGTCTGAAA | 672 |
rs80357905 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070973 | AACAGAAAGGGTCAA[-/C]AAAAGAATGTCCATG | 672 |
rs80357907 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071169 | CTGATCCTTCTGAAG[-/A]CAGAGCCCCAGAGTC | 672 |
rs80357908 | in-del | -/C | 1.65067e-05 | 0.00287282 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43094021 | ACAAATAAATTAAAG[-/C]GTAAAAGGAGACCTA | 672 |
rs80357909 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093294 | CTAATAATGCTGAAG[-/G]ACCCCAAAGATCTCA | 672 |
rs80357910 | in-del | -/AGGAAGATACT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092042 | ATGATGGTGAAATAA[-/AGGAAGATACT]AGTTTTGCTGAAAAT | 672 |
rs80357911 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094521 | GGACTCCCAGCACAG[-/A]AAAAAAGGTAGATCT | 672 |
rs80357912 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092914 | TCATTTGCTCCGTTT[-/T]TCAAATCCAGGAAAT | 672 |
rs80357913 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093155 | AGTTAGCACTCTAGG[-/G]AAGGCAAAAACAGAA | 672 |
rs80357914 | in-del | -/AG | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124027 | CAGAAAATCTTAGAG[-/AG]TGTCCCATCTGGTAA | 672 |
rs80357915 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074394 | GATGTGGAGGAGCAA[-/G]CAGCTGGAAGAGTCT | 672 |
rs80357916 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076581 | AAAGTAGTGAATACC[-/C]TATAAGCCAGAATCC | 672 |
rs80357917 | in-del | -/AATC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092803 | GAACAAAAGGAAGAA[-/AATC]AAGGAAAGAATGAGT | 672 |
rs80357918 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091661 | TTAGTGAGGAAACAA[-/AA]TGTTCTGCTAGCTTG | 672 |
rs80357919 | in-del | -/CTCA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094685 | AAATACTCATGCCAG[-/CTCA]TTACAGCATGAGAAC | 672 |
rs80357920 | in-del | -/TTAAAG | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092419 | TTAGAGAAAATGTTT[-/TTAAAG]AAGCCAGCTCAAGCA | 672 |
rs80357921 | in-del | -/AA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091000 | GTGTGAGAGTGAAAC[-/AA]GCGTCTCTGAAGACT | 672 |
rs80357922 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093535 | AGGCACAGCAGAAAC[-/C]TACAACTCATGGAAG | 672 |
rs80357923 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092317 | AACATTCAAGCAGAA[-/C]TAGGTAGAAACAGAG | 672 |
rs80357924 | in-del | -/AACT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067651 | ACACCACATCACTTT[-/AACT]AATCTAATTACTGAA | 672 |
rs80357925 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057070 | TCCAAAGCGAGCAAG[-/A]GAATCCCAGGACAGA | 672 |
rs80357926 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091910 | CCGAAGAGGGGCCAA[-/A]GAAATTAGAGTCCTC | 672 |
rs80357927 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093719 | TATCCACAATTCAAA[-/A]GCACCTAAAAAGAAT | 672 |
rs80357928 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091769 | CGAGTGTCTGTCTAA[-/TT]GAACACAGAGGAGAA | 672 |
rs80357929 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092663 | GTTTTGTCTATCATC[-/T]CAGTTCAGAGGCAAC | 672 |
rs80357930 | in-del | -/CT | 1.64819e-05 | 0.00287066 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43093315 | AACTAGAAACAGTTA[-/CT]AAGTGTCTAATAATG | 672 |
rs80357932 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093638 | AGTCAGTAGAAATCT[-/T]AAGCCCACCTAATTG | 672 |
rs80357933 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093619 | CCACCTAATTGTACT[-/G]AATTGCAAATTGATA | 672 |
rs80357934 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047692 | CCAGGGTGTCCACCC[-/A]ATTGTGGTTGTGCAG | 672 |
rs80357935 | in-del | -/ATCT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091017 | GTGAAGCAGCATCTG[-/ATCT]GGTGTGAGAGTGAAA | 672 |
rs80357936 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093328 | GAAAAAGAAGAGAAA[-/C]TAGAAACAGTTAAAG | 672 |
rs80357937 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092518 | GAGGAAAACTTTGAG[-/G]AACATTCAATGTCAC | 672 |
rs80357938 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067677 | CTCGTGTACAAGTTT[-/G]CCAGAAAACACCACA | 672 |
rs80357939 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094175 | TCACTCCAAATCAGT[-/A]GAGAGTAATATTGAA | 672 |
rs80357940 | in-del | -/CC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093492 | CAACTGGAGCCAAGA[-/CC]AGAGTAACAAGCCAA | 672 |
rs80357941 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094855 | ATATTTTCAGCTGCT[-/T]GTGAATTTTCTGAGA | 672 |
rs80357942 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092782 | AAGAATGAGTCTAAT[-/A]ATCAAGCCTGTACAG | 672 |
rs80357943 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115736 | ACAAAGTGTGACCAC[-/A]TATTTTGCAAGTAAG | 672 |
rs80357944 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093332 | AGAAGAAAAAGAAGA[-/G]AAACTAGAAACAGTT | 672 |
rs80357945 | in-del | -/GT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092172 | GAAGTAGTTCAGACT[-/GT]TAATACAGATTTCTC | 672 |
rs80357946 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047670 | GTTGTGCAGCCAGAT[-/G]CCTGGACAGAGGACA | 672 |
rs80357947 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094013 | ATTAAAGCGTAAAAG[-/G]AGACCTACATCAGGC | 672 |
rs80357948 | in-del | -/C/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092918 | CCAGTCATTTGCTCC[-/C/T]GTTTTCAAATCCAGG | 672 |
rs80357949 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115747 | GAACCTGTCTCCACA[-/AA]GTGTGACCACATATT | 672 |
rs80357950 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104246 | ATGCAAACAGCTATA[-/A]TTTTGCAAAAAAGGA | 672 |
rs80357951 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115730 | TGTGACCACATATTT[-/T]GCAAGTAAGTTTGAA | 672 |
rs80357952 | in-del | -/AGAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093705 | CAAAAGCACCTAAAA[-/AGAA]TAGGCTGAGGAGGAA | 672 |
rs80357953 | in-del | -/G | 1.64749e-05 | 0.00287005 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43094608 | AATTCTGTAATAAAA[-/G]CAAACAGCCTGGCTT | 672 |
rs80357954 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094443 | TGCCATGCTCAGAGA[-/A]TCCTAGAGATACTGA | 672 |
rs80357955 | in-del | -/CT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094736 | AGTATCAGGGTAGTT[-/CT]GTTTCAAACTTGCAT | 672 |
rs80357956 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091982 | GCAAAAGCGTCCAGA[-/AA]GGAGAGCTTAGCAGG | 672 |
rs80357957 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093217 | AGCAGTATTTCATTG[-/G]TACCTGGTACTGATT | 672 |
rs80357959 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051091 | GCTAGAAATCTGTTG[-/C]TATGGGCCCTTCACC | 672 |
rs80357960 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093268 | CTCATGTTAAGTGGA[-/G]AAAGGGTTTTGCAAA | 672 |
rs80357961 | in-del | -/TCTCA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092661 | AGGTTTTGTCTATCA[-/TCTCA]GTTCAGAGGCAACGA | 672 |
rs80357962 | in-del | -/CC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092919 | CGCCAGTCATTTGCT[-/CC]GTTTTCAAATCCAGG | 672 |
rs80357963 | in-del | -/TGTC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091773 | TTGCTACCGAGTGTC[-/TGTC]TAAGAACACAGAGGA | 672 |
rs80357964 | in-del | -/GACGTTC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094285 | GTAGCTGATGTATTG[-/GACGTTC]TAAATGAGGTAGATG | 672 |
rs80357965 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094722 | CTGTTTCAAACTTGC[-/A]TGTGGAGCCATGTGG | 672 |
rs80357966 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092198 | TGAAATAAAAAAGCA[-/A]GAATATGAAGAAGTA | 672 |
rs80357967 | in-del | -/TAACATTAGAGAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092430 | ATAACATTAGAGAAA[-/TAACATTAGAGAAA]ATGTTTTTAAAGAAG | 672 |
rs80357968 | in-del | -/GC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092969 | AAGTGAACTTGATGC[-/GC]TCAGTATTTGCAGAA | 672 |
rs80357969 | in-del | -/AG | 3.29647e-05 | 0.00405971 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43094170 | TCCAAATCAGTAGAG[-/AG]TAATATTGAAGACAA | 672 |
rs80357970 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093056 | AGATAATAGAAATGA[-/C]ACAGAAGGCTTTAAG | 672 |
rs80357971 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092849 | CTGGGTCCTTAAAGA[-/AA]CAAAGTCCAAAAGTC | 672 |
rs80357972 | in-del | -/TG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115742 | TGTCTCCACAAAGTG[-/TG]ACCACATATTTTGCA | 672 |
rs80357973 | in-del | -/ATTGGGCA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045793 | TCTCTGTCTCCAGCA[-/ATTGGGCA]GATGTGTGAGGCACC | 672 |
rs80357974 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067625 | CTGAAGAGACTACTC[-/C]ATGTTGTTATGAAAA | 672 |
rs80357975 | in-del | -/GAAA | 1.6659e-05 | 0.00288604 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43063346 | AGTCTATTAAAGAAA[-/GAAA]AATGCTGAATGAGGT | 672 |
rs80357976 | in-del | -/A | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045780 | GCAGATGTGTGAGGC[-/A]CCTGTGGTGACCCGA | 672 |
rs80357977 | in-del | -/GT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082509 | TGAACTAGAAGCTGT[-/GT]TAGAACAGCATGGGA | 672 |
rs80357978 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094195 | AATATGTAAAAGTGA[-/AA]GAGTTCACTCCAAAT | 672 |
rs80357979 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091565 | GATTGGTTCTTCCAA[-/A]CAAATGAGGCATCAG | 672 |
rs80357980 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091919 | TCAGGGTTACCGAAG[-/A]GGGGCCAAGAAATTA | 672 |
rs80357981 | in-del | -/G | 1.64749e-05 | 0.00287005 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43082518 | GAAATGGCTGAACTA[-/G]AAGCTGTGTTAGAAC | 672 |
rs80357982 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093329 | AGAAAAAGAAGAGAA[-/A]CTAGAAACAGTTAAA | 672 |
rs80357984 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092690 | CCAAATGTAGTATCA[-/AA]GGAGGCTCTAGGTTT | 672 |
rs80357985 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094366 | GAGTGGTTTTCCAGA[-/A]GTGATGAACTGTTAG | 672 |
rs80357986 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091770 | CCGAGTGTCTGTCTA[-/T]AGAACACAGAGGAGA | 672 |
rs80357987 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091559 | TTCTTCCAAACAAAT[-/G]AGGCATCAGTCTGAA | 672 |
rs80357989 | in-del | -/TCATTAC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094680 | ATGCCAGCTCATTAC[-/TCATTAC]AGCATGAGAACAGCA | 672 |
rs80357990 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093175 | GAAAGTATCTCGTTA[-/A]CTGGAAGTTAGCACT | 672 |
rs80357991 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092532 | AGAAAAATCTGCTAG[-/A]GGAAAACTTTGAGGA | 672 |
rs80357992 | in-del | -/CT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092238 | GTCTATAAACAAAGT[-/CT]TCCTGGAAGTAATTG | 672 |
rs80357993 | in-del | -/AG | 1.64749e-05 | 0.00287005 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43091760 | TGTCTAAGAACACAG[-/AG]GAGAATTTATTATCA | 672 |
rs80357994 | in-del | -/CATT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092512 | GAAAACTTTGAGGAA[-/CATT]CAATGTCACCTGAAA | 672 |
rs80357996 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092200 | CCTGAAATAAAAAAG[-/A]CAAGAATATGAAGAA | 672 |
rs80357997 | in-del | -/G | 1.6604e-05 | 0.00288127 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43063889 | GCGGGAGGAAAATGG[-/G]TAGTTAGCTATTTCT | 672 |
rs80357998 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092732 | CTTTCCTGTGGTTGG[-/T]CAGAAAGATAAGCCA | 672 |
rs80357999 | in-del | -/TG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093129 | ACAGAACCAAATAAA[-/TG]TGTGAGTCAGTGTGC | 672 |
rs80358000 | snp | A/T | 1.74452e-05 | 0.00295335 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43074539 | GCGATGGTTTTCTCC[A/T]TCCATTTATCTTTCT | 672 |
rs80358001 | snp | A/G | 1.64882e-05 | 0.00287121 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43104858 | TGGAGTGTAAGTGTT[A/G]AATATCCCAAGAATG | 672 |
rs80358002 | snp | A/G/T | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43047705 | CCTTCCTGGGGATCC[A/G/T]GGGTGTCCACCCAAT | 672 |
rs80358003 | snp | A/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124013 | GTGTCCCATCTGGTA[A/T]GTCAGCACAAGAGTG | 672 |
rs80358004 | snp | A/C/G/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43063332 | AAAATGCTGAATGAG[A/C/G/T]TAAGTACTTGATGTT | 672 |
rs80358005 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071245 | AAACTTCTCCCATTC[C/T]TTTCAGAGGGAACCC | 672 |
rs80358006 | snp | C/G/T | 0.00115867 | 0.0240428 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43115793 | TTTCTTTTTCTCCCC[C/G/T]CCTACCCTGCTAGTC | 672 |
rs80358007 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43091039 | ACCTCTGTTTTTGTT[A/G]TTTAAGGTGAAGCAG | 672 |
rs80358008 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43071239 | CTCCCATTCCTTTCA[A/G]AGGGAACCCCTTACC | 672 |
rs80358009 | snp | C/G/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43047641 | CAATGGCTTCCATGG[C/G/T]AAGGTGCCTGCATGT | 672 |
rs80358010 | snp | A/C/G/T | | | splice-donor-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124016 | AGAGTGTCCCATCTG[A/C/G/T]TAAGTCAGCACAAGA | 672 |
rs80358011 | snp | A/C/G/T | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43104263 | TCCCTTGTATTTTAC[A/C/G/T]GATGCAAACAGCTAT | 672 |
rs80358013 | snp | A/G | 6.60099e-05 | 0.00574461 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43097241 | CAACTTATTGCAGGT[A/G]AGTCAAAGAGAACCT | 672 |
rs80358014 | snp | G/T | 0.000333478 | 0.0129084 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43097306 | ATTGATTTATTTTTT[G/T]GGGGGAAATTTTTTA | 672 |
rs80358015 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43091432 | GATTCAAACTTAGGT[A/G]TTGGAACCAGGTTTT | 672 |
rs80358016 | snp | C/T | 1.65209e-05 | 0.00287405 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43082594 | TTCATTTTCTTGGTG[C/T]CATTTATCGTTTTTG | 672 |
rs80358017 | snp | A/G | 1.91988e-05 | 0.00309823 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43095942 | GTGTTTCTTATTAGG[A/G]CTCTGTCTTTTCCCT | 672 |
rs80358018 | snp | A/C/G | 1.83078e-05 | 0.00302549 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43115780 | CCCCCTACCCTGCTA[A/C/G]TCTGGAGTTGATCAA | 672 |
rs80358019 | snp | A/C/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43091034 | TGTTTTTGTTATTTA[A/C/G]GGTGAAGCAGCATCT | 672 |
rs80358020 | snp | A/C/G/T | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43094861 | TTTTGTATATTTTCA[A/C/G/T]CTGCTTGTGAATTTT | 672 |
rs80358021 | snp | C/G | 0.000167853 | 0.0091596 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43071246 | TAAACTTCTCCCATT[C/G]CTTTCAGAGGGAACC | 672 |
rs80358022 | snp | A/G | 0.00158116 | 0.0280727 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43076474 | AGGTAAGAAACATCA[A/G]TGTAAAGATGCTGTG | 672 |
rs80358023 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070925 | CCCAGAAGAATTTGT[C/G]AGTGTATCCATATGT | 672 |
rs80358025 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106553 | AATTAAATTGTTCTT[G/T]CTTTCTTTATAATTT | 672 |
rs80358026 | snp | C/T | | | splice-donor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43106454 | GATATAACCAAAAGG[C/T]ATATAATTTGGTAAT | 672 |
rs80358027 | snp | A/C/G/T | 1.64944e-05 | 0.00287175 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline)/C(germline) | 17:43082403 | GCACATCAGAAAAAG[A/C/G/T]TGTGTATTGTTGGCC | 672 |
rs80358028 | snp | A/G | | | splice-donor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43049120 | TTCACCCTTGGCACA[A/G]TAAGTATTGGGTGCC | 672 |
rs80358029 | snp | A/C/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43047704 | CTTCCTGGGGATCCA[A/C/G]GGTGTCCACCCAATT | 672 |
rs80358030 | snp | A/G/T | 1.64741e-05 | 0.00286998 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43099774 | TCTACATTGAATTGG[A/G/T]TAAGGGTCTCAGGTT | 672 |
rs80358031 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047634 | TTCCATGGTAAGGTG[C/T]CTGCATGTACCTGTG | 672 |
rs80358032 | snp | C/G | 0.000115717 | 0.00760559 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43067602 | ATGAAAACAGGTATA[C/G]CAAGAACCTTTACAG | 672 |
rs80358033 | snp | A/C/G | 5.49963e-05 | 0.00524363 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43095924 | CTGTCTTTTCCCTAT[A/C/G]GTGTGGGAGATCAAG | 672 |
rs80358034 | snp | C/T | 5.05153e-05 | 0.00502544 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43090935 | CACTCAGGTAAAAAG[C/T]GTGTGTGTGTGTGCA | 672 |
rs80358035 | snp | A/G | 0.00139937 | 0.0264145 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43067715 | AACTCATGATAATGG[A/G]ATATTTGATTTAATT | 672 |
rs80358036 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070860 | GAAAGAGTTTTATGT[A/G]GGTATTGTCAATTAA | 672 |
rs80358037 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104972 | TGAGTGTGTTTCTCA[A/G]ACAATTTAATTTCAG | 672 |
rs80358038 | snp | A/C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115721 | ATATTTTGCAAGTAA[A/C/G/T]TTTGAATGTGTTATG | 672 |
rs80358039 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115799 | ATTTATTTTCTTTTT[C/T]TCCCCCCCTACCCTG | 672 |
rs80358040 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049112 | TGGCACAGTAAGTAT[C/T]GGGTGCCCTGTCAGA | 672 |
rs80358041 | snp | A/C/G | 1.65718e-05 | 0.00287848 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43051062 | CCAACATGCCCACAG[A/C/G]TAAGAGCCTGGGAGA | 672 |
rs80358042 | snp | A/C/G/T | | | splice-donor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43106455 | TGATATAACCAAAAG[A/C/G/T]TATATAATTTGGTAA | 672 |
rs80358043 | snp | C/G/T | | | splice-donor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43115725 | CCACATATTTTGCAA[C/G/T]TAAGTTTGAATGTGT | 672 |
rs80358044 | snp | A/G/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43074330 | CAAGGCAAGATCTAG[A/G/T]TAATATTTCATCTGC | 672 |
rs80358045 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124012 | TGTCCCATCTGGTAA[A/G]TCAGCACAAGAGTGT | 672 |
rs80358046 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063867 | GCTATTTCTGTAAGT[A/G]TAATACTATTTCTCC | 672 |
rs80358047 | snp | A/T | 0.00151057 | 0.0274409 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43099773 | CTACATTGAATTGGG[A/T]AAGGGTCTCAGGTTT | 672 |
rs80358048 | snp | A/G/T | 1.64784e-05 | 0.00287035 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43045803 | TGTTCTCTGTCTCCA[A/G/T]CAATTGGGCAGATGT | 672 |
rs80358050 | snp | C/G/T | 0.0015949 | 0.028194 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43095838 | AAAAAAGGGTAATGG[C/G/T]AAAGTTTGCCAACTT | 672 |
rs80358051 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104264 | TTCCCTTGTATTTTA[C/G]AGATGCAAACAGCTA | 672 |
rs80358052 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097298 | ATTTTTTGGGGGGAA[A/G]TTTTTTAGGATCTGA | 672 |
rs80358053 | snp | A/G/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43067607 | TTGTTATGAAAACAG[A/G/T]TATACCAAGAACCTT | 672 |
rs80358054 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43074523 | TCCATTTATCTTTCT[A/G]GGTCATCCCCTTCTA | 672 |
rs80358055 | snp | C/G | 0.000646355 | 0.0179655 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43115791 | TCTTTTTCTCCCCCC[C/G]TACCCTGCTAGTCTG | 672 |
rs80358056 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067735 | CTGAGCTGTGTGCTA[C/G]AGGTAACTCATGATA | 672 |
rs80358057 | snp | A/G | 2.25716e-05 | 0.00335936 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091042 | TGAACCTCTGTTTTT[A/G]TTATTTAAGGTGAAG | 672 |
rs80358058 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43094875 | GAGTACCTTGTTATT[A/T]TTGTATATTTTCAGC | 672 |
rs80358059 | snp | A/T | 1.69367e-05 | 0.00290999 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43063960 | CTTTGAGTGTTTTTC[A/T]TTCTGCAGATGCTGA | 672 |
rs80358061 | snp | G/T | 1.65075e-05 | 0.00287289 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43104967 | GTGTTTCTCAAACAA[G/T]TTAATTTCAGGAGCC | 672 |
rs80358062 | snp | A/G/T | 3.29473e-05 | 0.00405864 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43047635 | CTTCCATGGTAAGGT[A/G/T]CCTGCATGTACCTGT | 672 |
rs80358063 | snp | A/G | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43076487 | ACCAGGAGTGGAAAG[A/G]TAAGAAACATCAATG | 672 |
rs80358064 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115723 | ACATATTTTGCAAGT[A/C]AGTTTGAATGTGTTA | 672 |
rs80358065 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43106535 | TTCTTTATAATTTAT[A/G]GATTTTGCATGCTGA | 672 |
rs80358066 | snp | A/C/T | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43063953 | TGTTTTTCATTCTGC[A/C/T]GATGCTGAGTTTGTG | 672 |
rs80358067 | snp | C/G | 1.68312e-05 | 0.00290092 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43071254 | GTGTAAATTAAACTT[C/G]TCCCATTCCTTTCAG | 672 |
rs80358069 | snp | A/C/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43057137 | TGTTTGGTTTCTTTC[A/C/G]GCATGATTTTGAAGT | 672 |
rs80358070 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43091033 | GTTTTTGTTATTTAA[A/G]GTGAAGCAGCATCTG | 672 |
rs80358071 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104295 | TACATTTTTCTCTAA[C/G]TGCAAACATAATGTT | 672 |
rs80358072 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43091043 | CTGAACCTCTGTTTT[C/T]GTTATTTAAGGTGAA | 672 |
rs80358073 | snp | A/C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049116 | CCCTTGGCACAGTAA[A/C/G/T]TATTGGGTGCCCTGT | 672 |
rs80358074 | snp | A/C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063868 | AGCTATTTCTGTAAG[A/C/G/T]ATAATACTATTTCTC | 672 |
rs80358076 | snp | A/G/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43090943 | ATTTTAACCACTCAG[A/G/T]TAAAAAGCGTGTGTG | 672 |
rs80358077 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076478 | GGAAAGGTAAGAAAC[A/G]TCAATGTAAAGATGC | 672 |
rs80358079 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057147 | TGATGGGTTGTGTTT[A/G]GTTTCTTTCAGCATG | 672 |
rs80358080 | snp | C/T | 6.60099e-05 | 0.00574461 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43082586 | CTTGGTGCCATTTAT[C/T]GTTTTTGAAGCAGAG | 672 |
rs80358081 | snp | A/G | 1.84225e-05 | 0.00303495 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43095926 | CTCTGTCTTTTCCCT[A/G]TAGTGTGGGAGATCA | 672 |
rs80358082 | snp | A/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074328 | AGGCAAGATCTAGGT[A/G/T]ATATTTCATCTGCTG | 672 |
rs80358083 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106453 | ATATAACCAAAAGGT[A/G]TATAATTTGGTAATG | 672 |
rs80358084 | snp | C/T | 3.31087e-05 | 0.00406857 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43049202 | TTACATCTAAATGTC[C/T]ATTTTAGATCAACTG | 672 |
rs80358085 | snp | G/T | 1.97638e-05 | 0.00314349 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43106551 | TTAAATTGTTCTTTC[G/T]TTCTTTATAATTTAT | 672 |
rs80358086 | snp | C/G/T | 1.64757e-05 | 0.00287012 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43070922 | AGAAGAATTTGTGAG[C/G/T]GTATCCATATGTATC | 672 |
rs80358087 | snp | A/C/T | 1.64754e-05 | 0.00287009 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43070924 | CCAGAAGAATTTGTG[A/C/T]GTGTATCCATATGTA | 672 |
rs80358088 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071249 | AATTAAACTTCTCCC[A/G]TTCCTTTCAGAGGGA | 672 |
rs80358089 | snp | C/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43067606 | TGTTATGAAAACAGG[C/T]ATACCAAGAACCTTT | 672 |
rs80358090 | snp | G/T | 9.88354e-05 | 0.00702908 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43057153 | TTATCCTGATGGGTT[G/T]TGTTTGGTTTCTTTC | 672 |
rs80358092 | snp | A/T | 0.00154555 | 0.0277559 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43049088 | TGTCAGAGAGGGAGG[A/T]CACAATATTCTCTCC | 672 |
rs80358094 | snp | A/C/G/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43063873 | TAGTTAGCTATTTCT[A/C/G/T]TAAGTATAATACTAT | 672 |
rs80358096 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43071240 | TCTCCCATTCCTTTC[A/G]GAGGGAACCCCTTAC | 672 |
rs80358098 | snp | A/C/T | 1.65619e-05 | 0.00287762 | BRCA1, NBR2 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43124010 | TCCCATCTGGTAAGT[A/C/T]AGCACAAGAGTGTAT | 672 |
rs80358099 | snp | A/C/G/T | 1.65993e-05 | 0.00288086 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline)/C(germline) | 17:43051118 | TCCTCTCTTCTTCCA[A/C/G/T]ATCTTCAGGGGGCTA | 672 |
rs80358100 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105033 | TTTTATTTGTTTACA[A/T]GTCTTTTCTTATTTT | 672 |
rs80358101 | snp | C/T | 0.000280257 | 0.0118343 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43104860 | TTTGGAGTGTAAGTG[C/T]TGAATATCCCAAGAA | 672 |
rs80358102 | snp | C/G | 3.79665e-05 | 0.00435681 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43095937 | TCTTATTAGGACTCT[C/G]TCTTTTCCCTATAGT | 672 |
rs80358104 | snp | A/C/G | 0.000101622 | 0.00712755 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43090934 | ACTCAGGTAAAAAGC[A/C/G]TGTGTGTGTGTGCAC | 672 |
rs80358105 | snp | C/G | 6.64662e-05 | 0.00576443 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43051131 | TGTCCCTCTCTCTTC[C/G]TCTCTTCTTCCAGAT | 672 |
rs80358107 | snp | A/G | 0.000399281 | 0.0141238 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43056974 | TTGCAGAGATGGGCC[A/G]CTTCATTTTGTAAGA | 672 |
rs80358108 | snp | A/C | 2.62795e-05 | 0.00362478 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43094862 | TTTTTGTATATTTTC[A/C]GCTGCTTGTGAATTT | 672 |
rs80358109 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063399 | CTTCTGCTGTATGTA[A/G]CCTGTCTTTTCTATG | 672 |
rs80358111 | snp | C/T | 0.000461635 | 0.0151857 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43076624 | ATTTGTTTTCTCATT[C/T]CATTTAAAGCAGTAT | 672 |
rs80358113 | snp | A/G | 0.000230798 | 0.0107399 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43104861 | GTTTGGAGTGTAAGT[A/G]TTGAATATCCCAAGA | 672 |
rs80358114 | snp | A/G | 1.6851e-05 | 0.00290263 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43063864 | ATTTCTGTAAGTATA[A/G]TACTATTTCTCCCCT | 672 |
rs80358115 | snp | G/T | 1.66399e-05 | 0.00288438 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43097302 | ATTTATTTTTTGGGG[G/T]GAAATTTTTTAGGAT | 672 |
rs80358116 | snp | A/C/G/T | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43104262 | CCCTTGTATTTTACA[A/C/G/T]ATGCAAACAGCTATA | 672 |
rs80358117 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115844 | TATTCACTAAGAATA[C/G]CTTTATTTTTAAATA | 672 |
rs80358119 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104959 | CAAACAATTTAATTT[C/G]AGGAGCCTACAAGAA | 672 |
rs80358121 | snp | A/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067764 | ACATATGCCATGGTG[A/G/T]AATAACTAGTATTCT | 672 |
rs80358122 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071248 | ATTAAACTTCTCCCA[A/T]TCCTTTCAGAGGGAA | 672 |
rs80358123 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106552 | ATTAAATTGTTCTTT[A/C]TTTCTTTATAATTTA | 672 |
rs80358124 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063871 | GTTAGCTATTTCTGT[A/C]AGTATAATACTATTT | 672 |
rs80358126 | snp | A/C/G | | | splice-acceptor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43049195 | TAAATGTCCATTTTA[A/C/G]ATCAACTGGAATGGA | 672 |
rs80358127 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115788 | TTTTCTCCCCCCCTA[C/G]CCTGCTAGTCTGGAG | 672 |
rs80358128 | snp | G/T | | | splice-donor-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124015 | GAGTGTCCCATCTGG[G/T]AAGTCAGCACAAGAG | 672 |
rs80358129 | snp | A/C | 6.67256e-05 | 0.00577567 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43063379 | TCTTTTCTATGATCT[A/C]TTTAGGGGTGACCCA | 672 |
rs80358130 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099751 | CTCAGGTTTTTTAAG[G/T]ATTTAATAATAATTG | 672 |
rs80358131 | snp | C/G/T | | | splice-donor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43115724 | CACATATTTTGCAAG[C/G/T]AAGTTTGAATGTGTT | 672 |
rs80358133 | snp | A/G | 3.3006e-05 | 0.00406226 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43097235 | ATTGCAGGTGAGTCA[A/G]AGAGAACCTTTGTCT | 672 |
rs80358136 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063861 | TCTGTAAGTATAATA[A/C]TATTTCTCCCCTCCT | 672 |
rs80358137 | snp | A/C/G/T | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43063374 | TCTATGATCTCTTTA[A/C/G/T]GGGTGACCCAGTCTA | 672 |
rs80358139 | snp | A/G | 0.000373978 | 0.0136693 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43090914 | TGTGTGTGCACATGC[A/G]TGTGTGTGGTGTCCT | 672 |
rs80358140 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104119 | AAATCCTTCCTTGGT[A/G]AAACCATTTGTTTTC | 672 |
rs80358143 | snp | C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082398 | TCAGAAAAAGGTGTG[C/G/T]ATTGTTGGCCAAACA | 672 |
rs80358144 | snp | A/G | 0.00023357 | 0.0108042 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094868 | TTGTTATTTTTGTAT[A/G]TTTTCAGCTGCTTGT | 672 |
rs80358145 | snp | A/G | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43047642 | ACAATGGCTTCCATG[A/G]TAAGGTGCCTGCATG | 672 |
rs80358146 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43104957 | AACAATTTAATTTCA[A/G]GAGCCTACAAGAAAG | 672 |
rs80358147 | snp | A/G | 5.49456e-05 | 0.00524116 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43106435 | TAATTTGGTAATGAT[A/G]CTAGGTTGGAAGCAA | 672 |
rs80358148 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051048 | GGTAAGAGCCTGGGA[C/G]AACCCCAGAGTTCCA | 672 |
rs80358149 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104863 | AGGTTTGGAGTGTAA[A/G]TGTTGAATATCCCAA | 672 |
rs80358150 | snp | A/C/G | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43057051 | TCCCAGGACAGAAAG[A/C/G]TAAAGCTCCCTCCCT | 672 |
rs80358151 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43045842 | CCTAGTCCAGGAGAA[A/T]GAATTGACACTAATC | 672 |
rs80358152 | snp | C/G/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43082402 | CACATCAGAAAAAGG[C/G/T]GTGTATTGTTGGCCA | 672 |
rs80358154 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097240 | AACTTATTGCAGGTG[A/G]GTCAAAGAGAACCTT | 672 |
rs80358155 | snp | A/C | | | splice-acceptor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43099882 | TTTACCATACTGTTT[A/C]GCAGGAAACCAGTCT | 672 |
rs80358157 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43045820 | ACACTAATCTCTGCT[A/T]GTGTTCTCTGTCTCC | 672 |
rs80358158 | snp | C/G/T | 1.79396e-05 | 0.00299491 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43106534 | TCTTTATAATTTATA[C/G/T]ATTTTGCATGCTGAA | 672 |
rs80358159 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104964 | TTTCTCAAACAATTT[A/C]ATTTCAGGAGCCTAC | 672 |
rs80358162 | snp | A/G/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43070927 | ACCCCAGAAGAATTT[A/G/T]TGAGTGTATCCATAT | 672 |
rs80358163 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104968 | TGTGTTTCTCAAACA[A/G]TTTAATTTCAGGAGC | 672 |
rs80358164 | snp | A/G | 1.66374e-05 | 0.00288417 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43097301 | TTTATTTTTTGGGGG[A/G]AAATTTTTTAGGATC | 672 |
rs80358165 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063869 | TAGCTATTTCTGTAA[A/G]TATAATACTATTTCT | 672 |
rs80358166 | snp | A/G | 4.97195e-05 | 0.00498571 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43051059 | ACATGCCCACAGGTA[A/G]GAGCCTGGGAGAACC | 672 |
rs80358167 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095839 | CAAAAAAGGGTAATG[A/G]CAAAGTTTGCCAACT | 672 |
rs80358169 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43091052 | CTTTTACATCTGAAC[C/T]TCTGTTTTTGTTATT | 672 |
rs80358170 | snp | A/C/T | 1.65872e-05 | 0.00287981 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43067706 | TAATGGAATATTTGA[A/C/T]TTAATTTCAGATGCT | 672 |
rs80358171 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097305 | TTGATTTATTTTTTG[A/G]GGGGAAATTTTTTAG | 672 |
rs80358172 | snp | A/G | 0.000544433 | 0.01649 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43082585 | TTGGTGCCATTTATC[A/G]TTTTTGAAGCAGAGG | 672 |
rs80358173 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43057136 | GTTTGGTTTCTTTCA[A/G]CATGATTTTGAAGTC | 672 |
rs80358174 | snp | C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106446 | CAAAAGGTATATAAT[C/G/T]TGGTAATGATGCTAG | 672 |
rs80358176 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43045819 | CACTAATCTCTGCTT[A/G]TGTTCTCTGTCTCCA | 672 |
rs80358178 | snp | A/G | 4.94972e-05 | 0.00497455 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091434 | TGGATTCAAACTTAG[A/G]TATTGGAACCAGGTT | 672 |
rs80358179 | snp | A/C/T | 5.61509e-05 | 0.00529833 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43115785 | TCTCCCCCCCTACCC[A/C/T]GCTAGTCTGGAGTTG | 672 |
rs80358180 | snp | A/G | 6.60917e-05 | 0.00574817 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43082387 | TGTGTATTGTTGGCC[A/G]AACACTGATATCTTA | 672 |
rs80358181 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067605 | GTTATGAAAACAGGT[A/G]TACCAAGAACCTTTA | 672 |
rs80358182 | snp | A/G/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43051061 | CAACATGCCCACAGG[A/G/T]AAGAGCCTGGGAGAA | 672 |
rs80358185 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076427 | TTTATATTGAACTCT[G/T]ATTGTTAATTTTTTT | 672 |
rs80358187 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097234 | TTGCAGGTGAGTCAA[A/G]GAGAACCTTTGTCTA | 672 |
rs80358189 | snp | A/G | 3.36785e-05 | 0.00410343 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43074522 | CCATTTATCTTTCTA[A/G]GTCATCCCCTTCTAA | 672 |
rs80358190 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051032 | AACCCCAGAGTTCCA[A/G]CACCAGCCTTTGTCT | 672 |
rs80358325 | in-del | -/GAT | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094424 | CCTAGAGATACTGAA[-/GAT]GTTCCTTGGATAACA | 672 |
rs80358326 | in-del | -/ATG | 8.23757e-05 | 0.00641725 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43094423 | CTAGAGATACTGAAG[-/ATG]TTCCTTGGATAACAC | 672 |
rs80358327 | in-del | -/TAT | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094083 | AACTGAAAATCTAAT[-/TAT]AGGAGCATTTGTTAC | 672 |
rs80358329 | in-del | -/TCT | 0.000643432 | 0.0179249 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43093686 | CTGAGGAGGAAGTCT[-/TCT]ACCAGGCATATTCAT | 672 |
rs80358331 | in-del | -/GCT | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093046 | GAAATGACACAGAAG[-/GCT]TTAAGTATCCATTGG | 672 |
rs80358332 | in-del | -/GTA | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092695 | ATAATGCCAAATGTA[-/GTA]TCAAAGGAGGCTCTA | 672 |
rs80358333 | in-del | -/GAGGAA | 1.65151e-05 | 0.00287355 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43092528 | AAGAAAAATCTGCTA[-/GAGGAA]AACTTTGAGGAACAT | 672 |
rs80358334 | in-del | -/AAA | 1.65255e-05 | 0.00287445 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43092202 | GCATCCTGAAATAAA[-/AAA]GCAAGAATATGAAGA | 672 |
rs80358335 | in-del | -/AAG | 0.000891221 | 0.0210907 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43092201 | CATCCTGAAATAAAA[-/AAG]CAAGAATATGAAGAA | 672 |
rs80358336 | in-del | -/AAG | 4.95323e-05 | 0.00497631 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43092185 | AGCAAGAATATGAAG[-/AAG]TAGTTCAGACTGTTA | 672 |
rs80358337 | in-del | -/AGT | 1.64947e-05 | 0.00287177 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43092111 | CAGCCTATGGGAAGT[-/AGT]CATGCATCTCAGGTT | 672 |
rs80358338 | in-del | -/CAG | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091688 | TTGGCAAAGGCATCT[-/CAG]GAACATCACCTTAGT | 672 |
rs80358339 | in-del | -/TTC | 4.94222e-05 | 0.00497078 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43091638 | TGCTAGCTTGTTTTC[-/TTC]ACAGTGCAGTGAATT | 672 |
rs80358340 | in-del | -/GAA | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091493 | GTTTCAGATGATGAA[-/GAA]AGAGGAACGGGCTTG | 672 |
rs80358341 | in-del | -/AAT | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091466 | GGCTTGGAAGAAAAT[-/AAT]CAAGAAGAGCAAAGC | 672 |
rs80358343 | in-del | -/CAC | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067663 | TTTGCCAGAAAACAC[-/CAC]ATCACTTTAACTAAT | 672 |
rs80358344 | in-del | -/GTT | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067618 | GAGACTACTCATGTT[-/GTT]ATGAAAACAGGTATA | 672 |
rs80358345 | in-del | -/GCT | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063947 | TTTCATTCTGCAGAT[-/GCT]GAGTTTGTGTGTGAA | 672 |
rs80358346 | in-del | -/CAG | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063363 | TCTTTAGGGGTGACC[-/CAG]TCTATTAAAGAAAGA | 672 |
rs80358347 | in-del | -/GAG | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057114 | ATTTTGAAGTCAGAG[-/GAG]ATGTGGTCAATGGAA | 672 |
rs80358348 | in-del | -/GTTGTG | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047680 | GTCCACCCAATTGTG[-/GTTGTG]CAGCCAGATGCCTGG | 672 |
rs80359871 | in-del | -/CGCGTTGAAGAAGTACAAAATGTCATTAA | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124050 | GATTTATCTGCTCTT[lengthTooLong]TGCTATGCAGAAAAT | 672 |
rs80359872 | in-del | -/CATAACAGATGGGCTGGAAGTAAGGAAACATGTAATGATAGGCGGACTCCCAGCACAGAAAAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094516 | TTAGCAAGGAGCCAA[lengthTooLong]AGGTAGATCTGAATG | 672 |
rs80359873 | in-del | -/TGACCCGAGAGTGG | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045759 | GTGAGGCACCTGTGG[-/TGACCCGAGAGTGG]GTGTTGGACAGTGTA | 672 |
rs80359874 | in-del | -/TGTTAGGTTCTGATGACTCACATGATGGGGAGTCTGAATC | 1.64963e-05 | 0.00287192 | BRCA1 | 17 | allele_origin=+.-----(germline)/0(germline) | 17:43094317 | CCAGAAGTGATGAAC[lengthTooLong]AAATGCCAAAGTAGC | 672 |
rs80359875 | in-del | -/GAATCCTAGAGATACTGAAGATGTTCCTTGGATAACACTAAATAGCAGCATTCAGA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094390 | ACTGCCATGCTCAGA[lengthTooLong]AAGTTAATGAGTGGT | 672 |
rs80359876 | in-del | -/CTGGCCTGACCCCAGAAGA | 1.64746e-05 | 0.00287002 | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070932 | TGTCCATGGTGGTGT[-/CTGGCCTGACCCCAGAAGA]ATTTGTGAGTGTATC | 672 |
rs80359877 | in-del | -/TGTCCCATCTG | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124017 | CAGAAAATCTTAGAG[-/TGTCCCATCTG]GTAAGTCAGCACAAG | 672 |
rs80359878 | in-del | -/TGTGGTGAAGGAGCTTTCATCATTCACC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049130 | GCTGTGTGGTGCTTC[-/TGTGGTGAAGGAGCTTTCATCATTCACC]CTTGGCACAGTAAGT | 672 |
rs80359879 | in-del | -/TTTGTGCTTTTCA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104888 | AGCTATTGAAAATCA[-/TTTGTGCTTTTCA]GCTTGACACAGGTTT | 672 |
rs80359880 | in-del | -/CAGAGAATCCT | 4.9423e-05 | 0.00497082 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43094439 | AGAAACTGCCATGCT[-/CAGAGAATCCT]AGAGATACTGAAGAT | 672 |
rs80359881 | in-del | -/ATGAATATTACTAATAGTG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093877 | CAGAATGGTCAAGTG[-/ATGAATATTACTAATAGTG]GTCATGAGAATAAAA | 672 |
rs80359882 | in-del | -/CTACTAGGCATAGCACCGT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091791 | ATATACCTTCTCAGT[-/CTACTAGGCATAGCACCGT]TGCTACCGAGTGTCT | 672 |
rs80359883 | in-del | -/CGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGAT | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045706 | GCACCTGTGGTGACC[lengthTooLong]ACCCCAGATCCCCCA | 672 |
rs80359884 | in-del | -/GGCCTGACCCCAGAAGAAT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070930 | TCCATGGTGGTGTCT[-/GGCCTGACCCCAGAAGAAT]TTGTGAGTGTATCCA | 672 |
rs80359885 | in-del | -/CAGAAAAGTAGTGAATA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076584 | GCAGTATTAACTTCA[-/CAGAAAAGTAGTGAATA]CCCTATAAGCCAGAA | 672 |
rs80359886 | in-del | -/AATAGTGGTCATGAGAATAAAACAAAAGGTGATTCTATTCAGAATGAGAAAAATCCTAACCCAATAGAATCACTCGAAAAAGAATCTGCTTTCAAAACGAAAGCTGAACCTATAAGCAGCAGTATAAGCAATATGGAACTCGAATTAAATATCCACAATTCAAAAGCACCTAAAAAGAATAGGCTGAGGAGGAAGTCTTCTACCAGGCATATT | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093671 | GTGATGAATATTACT[lengthTooLong]CATGCGCTTGAACTA | 672 |
rs80359887 | in-del | -/GCGTTGAAG | 1.65416e-05 | 0.00287586 | BRCA1, NBR2 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43124069 | ATTTATCTGCTCTTC[-/GCGTTGAAG]AAGTACAAAATGTCA | 672 |
rs80359888 | in-del | -/TTGAAAGTTCCCCAA | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071102 | TCTTCAACCTCTGCA[-/TTGAAAGTTCCCCAA]TTGAAAGTTGCAGAA | 672 |
rs111034213 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076501 | AGTAAAAATAAAGAA[C/G]CAGGAGTGGAAAGGT | 672 |
rs111312760 | snp | C/T | 0.5 | 0 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094369 | ACAGTTCATCACTTC[C/T]GGAAAACCACTCATT | 672 |
rs111387199 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101311 | AAGTGATCCTCCCAC[C/T]TCAGCCTCCCAAGGA | 672 |
rs111416097 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096189 | CAAGACCAGCCTGGC[A/C]AACATGGTGAAACCC | 672 |
rs111460805 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120532 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 672 |
rs111462026 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124741 | CTCATACATACCAGC[C/T]GGTGTTTTTTGTTTT | 672 |
rs111480954 | in-del | -/ATT | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098363 | TTATTATTTTTAAAA[-/ATT]ATTATTTTTTTGAGA | 672 |
rs111489251 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119289 | AAGAAAAAAAAAAAA[A/G]AAAAGGATCACAAGA | 672 |
rs111499627 | snp | C/G | 0.44651 | 0.154543 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072816 | TGATCTGCCCGCCTC[C/G]GCCTCCCAAAGTGCT | 672 |
rs111513157 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107345 | TGGGATTACAGGTGT[G/T]AGCCACCATGCCTGG | 672 |
rs111539978 | snp | C/T | 1.65111e-05 | 0.0028732 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093807 | AAAGCAGATTCTTTT[C/T]CGAGTGATTCTATTG | 672 |
rs111562492 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078140 | CCCAGGCTGGAATAC[A/C]GTGGCATGATCTCGG | 672 |
rs111562683 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048609 | AACCTCTGCCTCCCA[C/T]GTTCAAGCGATGCTC | 672 |
rs111563453 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052344 | GGAGTACAGTGGCAC[A/G]ATCATAGCTTGCTGC | 672 |
rs111564316 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111958 | AAAATACAATTAATA[A/C]AACAAAAGCATGGGG | 672 |
rs111572667 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110174 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 672 |
rs111581719 | snp | A/G | 0.203882 | 0.245709 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060745 | CTCCTGACCTCAAGT[A/G]ATTTGCCTGCCTTGG | 672 |
rs111611613 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057356 | CTCTACTAAAAATAC[A/G]AAAAATTAGTTGGGC | 672 |
rs111615606 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110340 | ACCTGTAATCCTAGC[A/G]CTTTGGGATGCCTAG | 672 |
rs111621189 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074794 | GGTGTGGTGGCTGGC[G/T]CCTGTAATCTCAGCT | 672 |
rs111720047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118688 | GCAATCTTCCTGCTT[C/T]GGCTTCCCAAAGTGC | 672 |
rs111791349 | snp | C/T | 0.00146012 | 0.0269801 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044565 | GCAACAGCTTCCTTC[C/T]TGGTGGGATCTGTCA | 672 |
rs111819368 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110965 | AATTAGCCATGCATG[G/T]TGGTGCACGCCTGTA | 672 |
rs111819895 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078938 | GGTGATGTGGCTCAC[A/G]CCTACAATCCCAGCA | 672 |
rs111870007 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108404 | TTTTACTAGCCAGGT[A/C]ATTTAACATTTATTA | 672 |
rs111956204 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125083 | GCCCCCTTCCTGATC[A/C]TCAGCGCTTCCCTCG | 672 |
rs112147727 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115955 | GGAACTGAGAATACA[A/G]CAGAGAATACGATCC | 672 |
rs112239971 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118668 | TCTTGAATGCCTGGC[A/C]TCAAGCAATCTTCCT | 672 |
rs112312822 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082827 | GATGTTATTGTGATG[C/T]CCTTTTGAAGTTGGT | 672 |
rs112316042 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070637 | CCTACTTGCTTTTAC[A/G]GATAGAAAGGAAAAT | 672 |
rs112349597 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066974 | AGGTGCCTGCCACCA[C/T]GCCCACCTAATTTTT | 672 |
rs112451052 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115960 | TGAGAATACAGCAGA[G/T]AATACGATCCTTACC | 672 |
rs112543237 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118676 | GCCTGGCATCAAGCA[A/G]TCTTCCTGCTTCGGC | 672 |
rs112674337 | snp | A/G | 0.030665 | 0.119967 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121006 | ACCTGGCAGGCGGAG[A/G]TTGCAGTGAGCCAAG | 672 |
rs112681719 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069832 | ATATTTCAGAATGAC[C/T]TGGTCATCTCTCAGT | 672 |
rs112704890 | in-del | -/G | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060745 | CTCCTGACCTCAAGT[-/G]ATTTGCCTGCCTTGG | 672 |
rs112757145 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056288 | AAGAGATACTCTCAA[C/T]TCAGCCTTCCGAGTA | 672 |
rs112885685 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102221 | GACTACAGGAGTCCG[C/T]CATCACGCTCAGCTA | 672 |
rs112891369 | in-del | -/C | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095586 | ACCCCATCTCAAAAA[-/C]AAAACAAACAAACAA | 672 |
rs112920552 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080357 | TGTGCCACCACGCCC[A/G]GCTAATTTTTTGTAG | 672 |
rs112960339 | snp | C/T | 0.00993419 | 0.0697739 | upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125524 | GAGCCAAGCGTCTCT[C/T]GGGGCTCTGGATTGG | 672 |
rs112966361 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066450 | AGAGTCTCACTCTGT[C/T]GCCAGGCTGGAGTGC | 672 |
rs113046417 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115968 | CAGCAGAGAATACGA[A/T]CCTTACCTTCAGTGA | 672 |
rs113117695 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123638 | CAGGCATAAGCCACC[A/G]CCCTCGGCCTCATCC | 672 |
rs113127132 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110292 | TTGAAAAGACAGAGC[C/T]AACTAAAATACTGGC | 672 |
rs113210086 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113054 | GTGATCCACCTGCCT[C/T]GGGCTCCAAAAGTGC | 672 |
rs113288336 | snp | C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119237 | TTTGGGAGGCCAAGG[C/G/T]GGGCCAGCCTGGGTG | 672 |
rs113322702 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090342 | GATACAGTAAGTGCC[A/G]TCATGTTTTTGCTAT | 672 |
rs113323025 | snp | A/G | 0.0103295 | 0.0711199 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125443 | GGAAACCAAGGGGCT[A/G]CCGCTAAGCAGCAGC | 672 |
rs113336506 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048622 | CACGTTCAAGCGATG[A/C]TCACACCTCAACTTC | 672 |
rs113410763 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105111 | ACATCTGTATAAACC[A/G]TGTGATGGCAGTGAT | 672 |
rs113472038 | in-del | -/A | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056675 | AGACTCCGTCTTGGG[-/A]AAAAAAAAAAAGAGA | 672 |
rs113488132 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060342 | CCACCACACCCAGCC[A/G]TGCCCAGCTAATTTT | 672 |
rs113655645 | snp | C/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097094 | ACACCAAATCCCAAG[C/T]CGTGTGTTTACCTAT | 672 |
rs113656989 | snp | C/T | 0.5 | 0 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094029 | CTTTTACGCTTTAAT[C/T]TATTTGTGAGGGGAC | 672 |
rs113657329 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061042 | AAGGCAGGAGAATTG[C/T]TTGAACCCAGGAGAC | 672 |
rs113716879 | snp | A/C | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099957 | AAGAGAAACTTGACA[A/C]CATGGACAAAATAAA | 672 |
rs113780543 | snp | A/G | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083992 | GCCTCAGCCTCTCAA[A/G]TAGCTGGGATTACAG | 672 |
rs113808892 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114021 | GGAGGTTGCAGTGAG[-/C]CCGAGATCACACCAC | 672 |
rs113814958 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067403 | GGGACTACAGGCGCA[C/T]GCGACCACACCCAGC | 672 |
rs113892722 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052001 | CTCTGAGAATGGCCA[C/T]TGTATCTTTAGGCCA | 672 |
rs114112971 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052636 | GTCTTGACCTTCCCA[C/T]TGCAATAAAAAGAAA | 672 |
rs114256395 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075955 | AAACTTAGTGGGTGT[A/G]GGTGGCGCATGCTTG | 672 |
rs114323360 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116451 | CCTCACTGCAGCCTT[C/G]AACTCCTGGGCTCAA | 672 |
rs114468819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095671 | ACATTAGTCTAGTAC[C/T]ATTTAAATCTATCAG | 672 |
rs115522763 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060996 | GGGTGTGGTAGCACG[C/T]GTGCCTGTAATACCA | 672 |
rs115632775 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095989 | GAACTGTCAAATGAC[A/C]AAGATCAAACATTTT | 672 |
rs115747310 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109029 | CAAAAAAACCCCAAC[C/T]ATATCTATATCTCTA | 672 |
rs115927772 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056683 | GTCTTGGGAAAAAAA[A/C]AAAGAGAGAGAGAGA | 672 |
rs116703787 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056199 | TTTTTTTCTTTTGAG[A/C]TCTTCTGTCTGTCGT | 672 |
rs116806238 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120293 | AGAAACCTAAAACAG[C/G]CTGAAAACCTTACCT | 672 |
rs117089582 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078027 | GGCGTGAGCCACTGC[A/G]CCCGACCGTTATTTT | 672 |
rs117151230 | snp | G/T | 0.0930568 | 0.194599 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052883 | AAGTCTGTGTGTTTT[G/T]TTTTTTTTTTTGAGA | 672 |
rs117230992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099245 | AACATATTTACACAT[A/G]TTTAAAACCAGATAT | 672 |
rs117281398 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097582 | ACAAAGTGAGACCCC[C/T]GTTTCTACTGAAAAC | 672 |
rs117381683 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117163 | TGATAAGCTTAAGGC[C/T]GGGCATGGTGCCTCA | 672 |
rs117690037 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074639 | GAGATCAGAAATGAC[G/T]GGCAAAAAAGAGCCC | 672 |
rs117845388 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058257 | CATGTGCCTGCAGTC[C/G]CAATTTCTTGAAAAG | 672 |
rs117979824 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073012 | ATGAGCAGTGGCTGT[A/C/G]ATCTGTCCTTATTTT | 672 |
rs137888201 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081037 | TTCAGAAATTAAGCA[C/T]TTCAGTTACAGATCT | 672 |
rs137892861 | snp | A/G | 3.78322e-05 | 0.0043491 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045620 | CCAGGGCCTGGAAAG[A/G]CCACTTTGTAAGCTC | 672 |
rs137894496 | snp | A/G | 4.9436e-05 | 0.00497148 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074457 | AGTTTCTATTCTGAA[A/G]ACTCCCAGAGCAACT | 672 |
rs137953573 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125703 | ATCGCTACCTATTGT[C/T]CAAAGCAGTCGTAAG | 672 |
rs137998759 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092857 | GACTTTGTTTCTTTA[A/G]GGACCCAGAGTGGGC | 672 |
rs138040784 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113156 | AGCACCTCAGCATCT[G/T]CCTGTAGAATTACTC | 672 |
rs138082324 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072263 | GCGTGGTGGTGCATG[C/T]CTGTAATCCCAGCTA | 672 |
rs138148964 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069393 | TTTTCCTCTTCGCTT[G/T]TTTAAAGACAACATG | 672 |
rs138167649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087374 | ACTTAAGAATTTTAA[C/T]GACCCAGGCTGAGTG | 672 |
rs138447886 | in-del | -/CA | 0.0292914 | 0.117421 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090922 | ACACACACGCATGTG[-/CA]CACACACACACGCTT | 672 |
rs138451202 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095316 | GCCAGGCACAGTGGC[A/T]CAAGCCTGTAACTGC | 672 |
rs138493864 | snp | A/G | 4.9717e-05 | 0.00498558 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43051091 | GGTGAAGGGCCCATA[A/G]CAACAGATTTCTAGC | 672 |
rs138544133 | in-del | -/GTGCGC | 0.0205511 | 0.0992634 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090737 | ATGTGTAGGCTGTGT[-/GTGCGC]GTGCGCGTGTGCGTG | 672 |
rs138580476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079718 | AGAGAAGCACACTTT[A/G]TGAGAACCAATGGGA | 672 |
rs138608489 | snp | A/C | 0.000153988 | 0.00877328 | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076504 | TTTCCACTCCTGGTT[A/C]TTTATTTTTACTGGT | 672 |
rs138690298 | in-del | -/GGGGGGGGG | 0.332621 | 0.308095 | cds-indel, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045689 | CAGTCAGTAGTGGCT[-/GGGGGGGGG]GTGGGGGATCTGGGG | 672 |
rs138782023 | snp | C/T | 0.00339174 | 0.041041 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044928 | CCTGCCTTAGCCACC[C/T]GAGTAGCTGGGATTA | 672 |
rs138794811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112307 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 672 |
rs138795459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117298 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCGCA | 672 |
rs138814568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060847 | AAACCAAGCTCTGGC[C/T]GGGCACAGTGGCTCA | 672 |
rs139038134 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065990 | ATAAACACTCTCCAA[C/T]TTGTCAGTGACCATG | 672 |
rs139191165 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122980 | AAGAATGGCATGAAC[C/T]CGGGAGGCAGAGTTT | 672 |
rs139210193 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051659 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCTCTCTGT | 672 |
rs139218576 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102743 | CTGTAGTCTACATCT[A/C]CTGGACTCAAGTGAT | 672 |
rs139237482 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046931 | TAATTTAACGATGTG[C/G]AAAAATGTATGTAAT | 672 |
rs139315471 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059077 | GTCAGAAGACTCCCA[A/T]GTTCATAGTCCTCCT | 672 |
rs139405471 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115430 | TCGCTTGAACTCGGG[A/G]GGCGGAGGTTGCAGT | 672 |
rs139416858 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102078 | CAGCTAAGTTTTTTT[G/T]TTTTTTTTTTGAGAC | 672 |
rs139433219 | snp | A/C | 1.64806e-05 | 0.00287054 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094652 | ATTCATTCTGTCTTT[A/C]GTGAGTAATAAACTG | 672 |
rs139448438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122039 | CTGATTTTCAATAAA[C/T]TGATAAATTGTGAAT | 672 |
rs139469099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072950 | TTGAACTCTTGGCCT[C/T]GAGCAATTCTCCCAC | 672 |
rs139650569 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059664 | AGTGTCACTCCTTCA[A/G]TTTCTCTTTACCTTA | 672 |
rs139650794 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061301 | CCTGGCCTCCTTAAA[C/T]GAAAGTAATCAACAA | 672 |
rs139678479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090110 | AGGCTAGATGGTCTC[C/T]ATTAGGAAGAGAACC | 672 |
rs139793550 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066699 | CTGATGCGAGCCACC[A/G]CGTCCAGCTGCCTCA | 672 |
rs139811854 | in-del | -/TTTTC | 0.204496 | 0.245824 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113363 | TTTTTCCTGGATGTA[-/TTTTC]TTTTCTTTTCTTTTT | 672 |
rs139858874 | snp | A/G | 1.64817e-05 | 0.00287064 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091480 | GATTATTTTCTTCCA[A/G]GCCCGTTCCTCTTTC | 672 |
rs139878952 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081188 | GTTTAGACTGAAGAT[A/G]GTGAAAGTACCCTAA | 672 |
rs139893476 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097444 | AGCTAGTATGTAATA[C/T]AGAGAAGTGGTTAAA | 672 |
rs140092494 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110062 | ACCACGCCTGGCTAA[C/G]TTTTTGTAATTTTAG | 672 |
rs140106612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119112 | GCAAGATATCAAAGA[A/G]CGACTAACCTGGCAG | 672 |
rs140225528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088781 | GCCTACGGCAGGTCA[A/G]AGAACATAAGCAAAC | 672 |
rs140253968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086697 | GGCAGATGTAATCAG[A/G]AATTGCAACCTTAAA | 672 |
rs140444440 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048864 | AACACAGTATGCTGG[A/G]GCAGTCACAGAGAGG | 672 |
rs140588714 | snp | A/C/G | 4.9423e-05 | 0.00497082 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43091727 | CTGGTTACTGCAGTC[A/C/G]TTTAAGCTATTCTTC | 672 |
rs140591536 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119415 | CAATGAACTAAGTCA[A/G]GAGGCTGGGTTTCTA | 672 |
rs140606703 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110876 | GAGGCTGAGGTGGGC[A/G]GATCACCTGAGGTCA | 672 |
rs140715757 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066127 | CTGCTTGTGTTAATA[C/T]GGCCCAGTTTCAAAT | 672 |
rs140725300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068502 | GACTGCTTGAGCTCA[A/G]GAGTCTGAGACCAAG | 672 |
rs140777892 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091817 | CCTAGTAGACTGAGA[A/G]GGTATATTGTTTACT | 672 |
rs140795918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064780 | TAGTTCAAAGCAAAT[A/G]TATTGGCTTTGAGTT | 672 |
rs140913990 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123682 | GCCATTTCAAGTGAT[A/G]GAGCTTGTTTTAGAG | 672 |
rs141048008 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046350 | ATTCTCCTGCCTCAG[C/T]CTCCCAAGTAGCAGG | 672 |
rs141094809 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073959 | ACAGGGTTTCACCAT[A/G]TTGGCCAGACAGGTC | 672 |
rs141203907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104685 | AAAATGTGCACCTTA[C/T]GATTGATAAAATAAG | 672 |
rs141245498 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054845 | CCTCCTGGGTTCAAC[C/T]GATTCTCTAGCCTCA | 672 |
rs141255461 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076588 | GGCTTATAGGGTATT[C/T]ACTACTTTTCTGTGA | 672 |
rs141292185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047156 | CCAGGCTGGAGTACA[C/G]TGGTGTGATCGTGGC | 672 |
rs141326951 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075488 | AACAATTATTGGGTG[A/C/T]TTACTATGGGTCAAA | 672 |
rs141444719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116383 | AATTATTATTACTTT[A/T]AAGATAAGGTCACAC | 672 |
rs141465583 | snp | A/G | 1.65127e-05 | 0.00287334 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092601 | GGTGGTATACGATAT[A/G]GGTTTTGTAAAAGTC | 672 |
rs141544169 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088488 | CATATAACATGTGTC[C/T]TTTGGTGTCCGGTTT | 672 |
rs141625477 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124476 | ACCAAAATCAACAAC[A/G]ACCAAACCAACACCA | 672 |
rs141660808 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074086 | TAGAGTACACCAAGA[C/T]TCCCTCATCCTCAAA | 672 |
rs141850147 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045096 | GGCGTGAGCCACCAT[A/G]CCCAGGTTTCAAGTT | 672 |
rs141883378 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117161 | AATGATAAGCTTAAG[A/G]CCGGGCATGGTGCCT | 672 |
rs141915184 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061077 | TTTGCAGTGAGCCAA[C/G]ATTGTGCCACTGCAC | 672 |
rs141916114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103533 | CTTGCTATGTTGCCT[G/T]GGCTGGTCTCAAACC | 672 |
rs142018359 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060615 | CCTGCCTCAGCCTCT[G/T]GAGTAGCTGGGATTA | 672 |
rs142024941 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110084 | TAATTTTAGTAGAGG[C/T]GGGGTTTCACCATGT | 672 |
rs142074233 | snp | A/C/G | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093931 | TTTGGTTAGTTCCCT[A/C/G]ATTTATCATTTCAGG | 672 |
rs142085161 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099453 | TTTTTTATTTTTTGG[C/T]ACAGACAGAGTTTCT | 672 |
rs142117419 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067387 | AGCCTCACGAGTAGC[C/T]GGGACTACAGGCGCA | 672 |
rs142221700 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062053 | GAATTATAAACAGAT[A/G]CATTTGCATGTATAT | 672 |
rs142296444 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096486 | TTGAGACAGGAGAAT[C/T]GCTTGAACCAGGGAG | 672 |
rs142310565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086340 | TTATTAATGAGAAGA[C/T]AAATTAATAAATAAG | 672 |
rs142383077 | snp | C/G | 1.64749e-05 | 0.00287005 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43091674 | CATTTTGTTTCCTCA[C/G]TAAGGTGATGTTCCT | 672 |
rs142395699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081082 | ACACACGTATATACC[A/G]AAGAGGAGATAGTAG | 672 |
rs142430564 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079653 | AGAAAAAGAAAGAAG[C/T]CAAAGAGAAAGGTAC | 672 |
rs142459158 | snp | A/G | 0.000231202 | 0.0107493 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43067690 | GGCAAACTTGTACAC[A/G]AGCATCTGAAATTAA | 672 |
rs142616110 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098662 | TGAGCCACCGCACCG[-/T]GCCAAAAATGTATTA | 672 |
rs142638930 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059351 | TGCCTGTAATCCCAG[A/C]TACTCGGGAGGCTGA | 672 |
rs142739377 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050648 | ATGTTCACCGAGAAT[A/C]TTCCCCTGCTCTGGG | 672 |
rs142808159 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108968 | ATTGCACTCCAGCCT[C/G]GGCAACAAGAGCGAA | 672 |
rs142829210 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066598 | GTATTTTTAGTAGAG[A/C]CTGGGTTTTACCATA | 672 |
rs142831199 | snp | C/T | 0.081446 | 0.184634 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121231 | ATACAAAAAATTAGC[C/T]GGGCATAGTGGTGGG | 672 |
rs142854457 | snp | C/G | 0.030665 | 0.119967 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101650 | TGGGATTACAGGTAC[C/G]TGCCACCACACCCAG | 672 |
rs142896455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117960 | TCTCATAGAGCTCAT[A/G]TTCTAGTGTGGTAGA | 672 |
rs143042094 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054613 | CCCAATTAATTTTTA[A/T]ATTTTTTTGTAGAGA | 672 |
rs143126962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075238 | AAAGTTGATCAATGT[C/T]GACATCTCTACACTC | 672 |
rs143160357 | snp | A/G | 0.000953379 | 0.0218124 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125337 | CTGAGAAACCCCACA[A/G]CCTGTCCCCCGTCCA | 672 |
rs143338062 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051690 | CACCTAGGCTGGAGC[A/G]TAGTGGTGCGATCTG | 672 |
rs143429315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048171 | AGTGTTGTGATTACA[A/G]GGGTGGGGCACTGGC | 672 |
rs143460481 | snp | C/G | 0.030665 | 0.119967 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098877 | GGCTGGAGTGCAATG[C/G]TGCGATCTTGGCTCA | 672 |
rs143496131 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097854 | ACTACTATAACTATT[C/T]TTACAATGCCTGTTG | 672 |
rs143578208 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080359 | TGCCACCACGCCCGG[A/C]TAATTTTTTGTAGTT | 672 |
rs143589966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074877 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 672 |
rs143652276 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116863 | TTACTTTTTCTCCCT[C/T]GTCATTTATTTTTAA | 672 |
rs143681310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052534 | AACACACTGGCATAG[A/G]TTCTTAGCAAATAAC | 672 |
rs143690995 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044195 | ATCCTAGGAGGTAGA[C/T]ACTATCATTACCCCC | 672 |
rs143757906 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111593 | TAGGGAGGCCAAGGC[A/G]GGCAGATCACGAGGT | 672 |
rs143849355 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123081 | AAAAAAAATACAAAA[A/G]TTAGCTGGGCATGGT | 672 |
rs143912779 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119205 | AGGTGCGGTGGCTCA[C/T]GCTGTAATCCCAGCA | 672 |
rs143920945 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093488 | TTCATTTGGCTTGTT[A/C]CTCTTCTTGGCTCCA | 672 |
rs143921429 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096529 | GTGAGCCGAGATGGC[G/T]CCACTACACTCCATC | 672 |
rs143935549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045964 | GTCTTGCTCTGTCGC[C/T]GAGGCTAGAGTGTGA | 672 |
rs143950975 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046252 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTTG | 672 |
rs144033340 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099711 | GACCAAGATTTTTGG[C/G]AAAACTATAAGATAA | 672 |
rs144034611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073208 | TCCCTATATTGTCCA[A/T]TTTGGGGGCAATGAG | 672 |
rs144110800 | in-del | -/T | 0.314787 | 0.241459 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087899 | ACTAAGCCTCACTAA[-/T]TTTTTTTTTTTTCCC | 672 |
rs144121044 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095712 | GACATTTGACAGAGA[A/T]TGATACTCTAACTCT | 672 |
rs144412026 | snp | C/T | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126870 | GGAACTGGGGCTGCG[C/T]GCAGCGCTCGCCAGC | 672 |
rs144440811 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073103 | TTGGGAGGCCAAGGT[A/C]GGAAGATTGCATGAG | 672 |
rs144477667 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114846 | GAAAAGGAGAAAGCC[C/T]ACTTGTTCTACTAAA | 672 |
rs144588397 | snp | A/G | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43071069 | AGTAGTATGAGCAGC[A/G]GCTGGACTCTGGGCA | 672 |
rs144689288 | in-del | -/G | 0.0372196 | 0.131242 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125795 | GTAATAAGGATTGTT[-/G]GGGGGGGTGGAGGGA | 672 |
rs144698700 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094306 | CCAATACATCAGCTA[C/G]TTTGGCATTTGATTC | 672 |
rs144792613 | snp | C/T | 1.6569e-05 | 0.00287824 | BRCA1, NBR2 | 17 | allele_origin=T(germline)/C(germline) | 17:43124077 | TGTACTTCTTCAACG[C/T]GAAGAGCAGATAAAT | 672 |
rs144813115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051936 | CACTGCGCCCGGCCC[C/T]CTCTGACTTTCTTCT | 672 |
rs144853230 | snp | A/G/T | 1.65353e-05 | 0.00287531 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43092551 | GCAGATTTTTCTTAC[A/G/T]TTTAGTTTTAACAAA | 672 |
rs144905732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102858 | CAAGGACTTGCTATG[C/T]TGCCCAAACTGGTCT | 672 |
rs145019951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112152 | TAGAGTACAGTGGCA[C/T]GATCTCAACTCACTG | 672 |
rs145050926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053389 | AGTTTCGGGCTTGGC[A/G]TAGTGGCTCACGCCT | 672 |
rs145157551 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120426 | GAAGTGAAATATGAT[C/T]CCTATCCTAGAACTT | 672 |
rs145225180 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047013 | ACACGTGTATATATA[C/T]GCACATATGCCTGGT | 672 |
rs145393880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083677 | GAGGGAAGGATCCAA[C/G]AGAAAGAGCCCTGAG | 672 |
rs145466894 | snp | A/C/G | 3.301e-05 | 0.00406252 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43071179 | CTCTGTCTTCAGAAG[A/C/G]ATCAGATTCAGGGTC | 672 |
rs145501518 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102079 | AGCTAAGTTTTTTTG[G/T]TTTTTTTTTGAGACA | 672 |
rs145647572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089089 | AGGCTGAGACGGGTG[A/G]ATTATTTGAGGTCAG | 672 |
rs145654477 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066220 | CAGAGGTCTCCTGTA[C/T]TACACAAGTTATAAT | 672 |
rs145668291 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098424 | AGTGCAGTGGTGTAG[C/T]GTTGGCTCATTGTAA | 672 |
rs145758886 | snp | A/C/T | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43049156 | AAAGCTCCTTCACCA[A/C/T]AGAAGCACCACACAG | 672 |
rs145781396 | snp | C/G | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 17:43090419 | CACTTTGTCACCCAG[C/G]CTGGAGTGCAGTGGT | 672 |
rs145869415 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068755 | CTTAAAACCAAGACT[C/T]AACCCTCTGATAGTT | 672 |
rs145903082 | snp | C/G/T | 1.64762e-05 | 0.00287016 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43091781 | GTTCTTAGACAGACA[C/G/T]TCGGTAGCAACGGTG | 672 |
rs145938998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081129 | AAAGTCACACAATAA[C/T]AACATTTTAAATCTT | 672 |
rs145956834 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077820 | CTCACCACAACCTCT[C/G]TGCCTCCCAGGTTCA | 672 |
rs145983188 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117215 | GGGAGGCTGAGGTGG[C/G]TGGATCACCTGAGCT | 672 |
rs146059433 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108991 | AGAGCGAAACTCCAT[C/T]TCAAAAACAAAACAA | 672 |
rs146079169 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101793 | AGGTGCAAGCTACTA[C/T]GCCCAGCCCCAGAAT | 672 |
rs146085503 | snp | A/G | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43104881 | ACACTCCAAACCTGT[A/G]TCAAGCTGAAAAGCA | 672 |
rs146201713 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122970 | GCTCAGGCAGAAGAA[C/T]GGCATGAACCCGGGA | 672 |
rs146299550 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061103 | TGCACTCCAGCCTGG[C/G]GGATAGAGGGAGACA | 672 |
rs146318688 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058377 | AGACTCTGCTAAAAA[A/C]AAACACACACACACA | 672 |
rs146467457 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120979 | TGAGGCAGGAGAAGC[A/G]CTTGAACTTGAACCT | 672 |
rs146595490 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072109 | AATAAGAGTACAGGC[C/T]GGGTGCGGTGGCTCA | 672 |
rs146602768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116143 | CATCTTTAAGCTCCA[C/T]AAAGACAAAATTTTC | 672 |
rs146719936 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048312 | GGTTCAAGCGATTCT[C/T]CTGCCCCAGCCCCTC | 672 |
rs146853830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073326 | CATTACTTTTTTCAC[G/T]TAATAAATCAGCAGA | 672 |
rs146891355 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119336 | AACCTTATTGTGAAG[A/C/G]GTTGTAATACAACTC | 672 |
rs146934045 | in-del | -/CTATCTATCTACCTAC | 0.452842 | 0.146134 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109041 | ACTATATCTATATCT[-/CTATCTATCTACCTAC]CTATCTATCTACCTA | 672 |
rs146959162 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060163 | ACAACCTCCACCTCC[C/T]GGGTTGATGAAGTGA | 672 |
rs146993095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124740 | TCTCATACATACCAG[C/T]CGGTGTTTTTTGTTT | 672 |
rs147055444 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074654 | TGGCAAAAAAGAGCC[C/T]GCAAGACAGCCTAGA | 672 |
rs147065412 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079069 | GCTGGGCGTGGTGGC[A/G]GGTGCCTGTAATCCC | 672 |
rs147144902 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067343 | CACTGCAACCTCCAT[C/T]TCCCCGGTTCAAGTG | 672 |
rs147182130 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100338 | ATCACATCTGATAAC[-/TTTTTTTTTTTTTT]TTTTTTTTTTGTTTT | 672 |
rs147250224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090107 | GAAAGGCTAGATGGT[C/T]TCTATTAGGAAGAGA | 672 |
rs147297981 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046253 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTTGT | 672 |
rs147307888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051371 | CTACAGGCATTCTTT[A/G]TCATTCAAGGACTGA | 672 |
rs147314539 | snp | A/G | 0.000853996 | 0.0206463 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095956 | GTCCTAATAAGAAAC[A/G]CTAGTTACATGTATG | 672 |
rs147403353 | snp | C/G/T | 0.00478085 | 0.0486577 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066655 | ACCTTGTGATCTGCC[C/G/T]GCCTCAGGCTCCCAA | 672 |
rs147420429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118065 | AGGTAGTTCAATATC[C/T]ATGTGGGGGTGAGAT | 672 |
rs147448807 | snp | C/T | 0.00100154 | 0.0223555 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091016 | TGTTTCACTCTCACA[C/T]CCAGATGCTGCTTCA | 672 |
rs147509580 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088583 | AAGTTTTCTATGATG[C/T]ACATATATAACTTTA | 672 |
rs147519994 | snp | A/C | 1.68165e-05 | 0.00289965 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43094798 | CAGTGGTGTTCAAAT[A/C]ATTATTACTGGGTTG | 672 |
rs147598602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060164 | CAACCTCCACCTCCC[A/G]GGTTGATGAAGTGAT | 672 |
rs147703239 | snp | A/G | 1.65688e-05 | 0.00287821 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071206 | GGTCATCAGAGAAGA[A/G]GCTGATTCCAGATTC | 672 |
rs147704942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079281 | TTGGCCAGAACCACC[A/G]TCTTTCAGTAATTTG | 672 |
rs147766773 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111066 | AGATTGTACCACTGC[A/G]CTCCAGCCTGGGCAA | 672 |
rs147777270 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060129 | AGGCTGGAGTGCAAT[A/G]GTGCGATCTCAGCTC | 672 |
rs147809611 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104331 | TATAATCAAAGAAAC[C/T]AAGAGAAACCCTATG | 672 |
rs147838900 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062593 | GGATATCCTGGTTTG[C/T]GCTGCAAAATTTTTT | 672 |
rs147856441 | in-del | -/AAG | 0.0185599 | 0.0945276 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104084 | AGAAAAAAAAAAGAA[-/AAG]AAGAAGAAGAAGAAG | 672 |
rs147915562 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124285 | AAAGATTCTAGAAGT[C/T]GCTTTTTGTAATTAG | 672 |
rs147946603 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082113 | CCAATTTCTCCCATT[C/T]CACTTAGCTTCCAAT | 672 |
rs148038877 | snp | A/C/T | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43091895 | AGATAAGTTCTCTTC[A/C/T]GAGGACTCTAATTTC | 672 |
rs148068102 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121405 | AACAAAACAAAAAGT[C/T]TGGGAGCGGTGGCTC | 672 |
rs148120486 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116981 | GCCTTATTTCCTATA[A/T]ACTAGACTTACAGGC | 672 |
rs148133790 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067256 | TCTTATTTTTTCACG[-/T]TTTTTTTTTTTTTTT | 672 |
rs148136491 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060439 | GGGATCTGCCTGCCT[C/T]GGCCTCCTAGAGTGC | 672 |
rs148141374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046002 | ATCTCGGCTCATTCA[A/G]CCTCCGCCTCCTGGG | 672 |
rs148196794 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125376 | CAGCGAGCTCACGCC[A/G]CGCAGTCGCAGTTTT | 672 |
rs148285379 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075374 | TAGAAAAGCATACAC[A/G]CCCAGTAAATAGTTC | 672 |
rs148341992 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107458 | CAATCTCAGCTCACT[A/G]CAACCTCCACCTCCT | 672 |
rs148353570 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088049 | AAGCCACTGTGCCTA[A/G]CTTCCTGGATATATT | 672 |
rs148436838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073159 | CAACATAACAAGACC[C/T]GTGTCTAACCCCACC | 672 |
rs148500539 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100863 | CAGCCTCCCGAGTAG[C/T]TGGGACTACAGGCGT | 672 |
rs148509734 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051983 | GTTCCTTCCTTCTCA[C/G]TACTCTGAGAATGGC | 672 |
rs148589356 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123509 | CACATGCCACTACGC[A/C]CAGCTAATTTTTGTA | 672 |
rs148902388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098588 | ATCCAGGCTGGTCTC[A/G]AACTCTGACCTCAGG | 672 |
rs148953585 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090589 | CATGTTGGCCAGGCT[A/G]GTCTCAAACTTCTGA | 672 |
rs148963975 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43043851 | GTTAGAAAGATACAG[C/T]AGTCAGCAAGATTCA | 672 |
rs149071245 | in-del | -/AGA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104100 | AGAAGAAGAAGAAGA[-/AGA]AGAAAACAAATGGTT | 672 |
rs149141411 | in-del | -/A | 0.445328 | 0.156035 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123064 | AAAAAGAAAAAAAAA[-/A]TACAAAAATTAGCTG | 672 |
rs149170015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120941 | CGGTGGCGTGCGCCT[A/G]TAATCCCAGCTACTC | 672 |
rs149174271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085439 | ACTATATAATTGTTA[A/G]TCATTACTGCCATTA | 672 |
rs149179857 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065333 | CGGCAATGTGTCCAA[A/G]GGGTTTAGATCCTCT | 672 |
rs149328571 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080091 | AGAGATCCAGAGTCC[A/C]AGTTTCAGAATATTA | 672 |
rs149349675 | snp | C/T | 0.000153988 | 0.00877328 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094304 | GTCCAATACATCAGC[C/T]ACTTTGGCATTTGAT | 672 |
rs149379936 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123350 | CACCGATCATCCATG[-/T]TTTTTTTTTTTTTTT | 672 |
rs149402012 | snp | A/G | 0.00104337 | 0.0228165 | BRCA1, NBR2 | 17 | allele_origin=G(germline)/A(germline) | 17:43124076 | TTGTACTTCTTCAAC[A/G]CGAAGAGCAGATAAA | 672 |
rs149469770 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118218 | TACACAGGCATGGTC[A/G]TGCTCAGGGTTTGCC | 672 |
rs149522050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113262 | GCCTCCTCTTGGACC[C/T]TCTCTTTCTTGCAAA | 672 |
rs149635371 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057558 | AAAAAAAATTAGGCC[A/G]GGTGTGGTGGCTCAC | 672 |
rs149736042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060065 | CACATGCCACCATTC[C/T]CAGCTAATTTTTTTT | 672 |
rs149765996 | in-del | -/GAGCCCTTCAGCCCGCCACTGC | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126748 | CTGGCCGTGCTGGAG[-/GAGCCCTTCAGCCCGCCACTGC]GCTGTGGGGGCCCCT | 672 |
rs149867679 | snp | C/T | 0.00021497 | 0.0103653 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094724 | ACATGGCTCCACATG[C/T]AAGTTTGAAACAGAA | 672 |
rs149949159 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102801 | GGGACTACAGGCACA[C/T]ACCACCATGCCCAGA | 672 |
rs149958317 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053035 | GTGCACACCACCACA[C/G/T]CCGGCTAATTTTTTG | 672 |
rs150043511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116122 | TATCACTGTGGGTGC[A/T]CATCTCATCTTTAAG | 672 |
rs150105864 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064906 | CTGGATCTCAGCTCA[C/T]GGCAAGCTCTGCCTC | 672 |
rs150150951 | in-del | -/AGGA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075074 | AAAGGACGGAAGGAA[-/AGGA]GGAAGGAAGGAAAGG | 672 |
rs150199798 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073960 | CAGGGTTTCACCATG[A/T]TGGCCAGACAGGTCT | 672 |
rs150347361 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086952 | GGTCTAGAGGGATTT[C/G]CTCTGTACAGAGAAT | 672 |
rs150411410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120222 | CAAAGAACTACCAAT[C/T]GTCAGAAATAGCTGC | 672 |
rs150421137 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102070 | CCACGCCCAGCTAAG[-/T]GTTTTTTTGTTTTTT | 672 |
rs150470020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108405 | TTTACTAGCCAGGTA[A/G]TTTAACATTTATTAC | 672 |
rs150513851 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121886 | TATTTTTATGACTCT[C/T]TCCCATGGAAATGAA | 672 |
rs150577181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072931 | TACATTGCCCAGGCT[A/G]GTCTTGAACTCTTGG | 672 |
rs150614759 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052188 | CACAATGTTCTATAT[C/T]TATGCTAATAAGGTA | 672 |
rs150670602 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081527 | TTAACACTCAGATAA[C/G]AATCACTGAGCTAGG | 672 |
rs150729791 | snp | A/G | 3.29745e-05 | 0.00406031 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067658 | ATTAGATTAGTTAAA[A/G]TGATGTGGTGTTTTC | 672 |
rs150988892 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044270 | AAAGTCGGCTGGCCT[A/G]AGTCTCAAGAACAGT | 672 |
rs151190044 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102713 | GCTGAAGTGCAGTGG[A/G]GTGATCATAGCTCAC | 672 |
rs151196052 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086485 | AAAAATCCCACTTCA[A/G]TAGTTTTTCCTGCCT | 672 |
rs151321765 | in-del | -/AG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056702 | GAGAGAGAGAGAGCA[-/AG]AGAGAGAGAGAGAAA | 672 |
rs180795814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071935 | ATGGCGTGTACCCGG[A/G]AGGCAGAGCTTGCAG | 672 |
rs180814404 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051309 | GTCCAGAACACTACT[A/G]GATTTCAGAAGATCT | 672 |
rs180891080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103130 | ATTTTAGATAAGCAT[A/C]ACAGAGCAGATAAAG | 672 |
rs180905862 | snp | C/T | 0.000384162 | 0.013854 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123966 | TTCTGTTCATTTGCA[C/T]AGGAGATAATCATAG | 672 |
rs180922283 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065013 | TTTTTTGTATTTTTA[C/G]TAGAGATGGGGTTTC | 672 |
rs180955947 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111261 | AAGGTGGCTCATGCC[A/T]GTAATCCTGGCACTG | 672 |
rs181080430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072517 | AAGTGATCTTCCTGT[C/T]TCAGCCTCCTGAGTA | 672 |
rs181098393 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111682 | AAAAAATTAGCTGGG[C/T]GTGGTGGCAGGCGTC | 672 |
rs181118693 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051761 | CCTGCCTTAGCCTCC[C/T]GAGTAGCTGGGATTA | 672 |
rs181344504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124610 | TCTACTTCCCTCTTG[C/G]GCTTTCTCAATGGCG | 672 |
rs181392764 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075589 | TTGTTTTGAGACGGA[A/G]TCTTGCTCTGTCGCC | 672 |
rs181430678 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046070 | GGAATTACAGGCACA[G/T]GCCATCACACCCAGC | 672 |
rs181436152 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057664 | CACGGTGAAACCCCG[A/T]CTCTACTTAAAATAC | 672 |
rs181582137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067524 | CTCCCAAAGTGCTGC[A/G]ATTACAGGCATGCGC | 672 |
rs181649512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089539 | TCCAGAAAGTAAAAT[C/T]GTGTACTTTCTTTTT | 672 |
rs181654250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107879 | CAACCAATATTTACT[A/G]TGTCTAGTACTATTC | 672 |
rs181675079 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068393 | TTATAAACCTACTAC[A/G]TACCACAAAACTTAA | 672 |
rs181723047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059929 | TATTATTTTTGAGAC[A/G]GAGTCTTGCTCTTTC | 672 |
rs181727428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106211 | TACAGCCCTACTTTA[C/T]ATAAGTCTGCAAGTT | 672 |
rs181732251 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127315 | GAGGATTTTATATGC[A/T]CCAGTCAGCACTCTG | 672 |
rs181732386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077112 | TAAACAAGACATGAG[C/T]GTCAGACATGAAAGA | 672 |
rs181752925 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059207 | AGTGGCTCACACCTG[C/T]AATCCCAGCACTTTG | 672 |
rs181758527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087761 | TGTTTTTGAGACAGG[A/G]TCTCACCATATCACC | 672 |
rs181765921 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117696 | GTGAGCCAAGATCGC[A/G]CCACTGTACTCCAAC | 672 |
rs181936042 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098566 | TAAAGAGGGGTTTCA[C/T]CAGGTTATCCAGGCT | 672 |
rs182008731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064398 | TGTAATGACAAATTT[C/T]CACCCCTAGAATGTC | 672 |
rs182009716 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081802 | TGGTTACTCCAATGG[C/T]ATCCTCTCAGAGGTC | 672 |
rs182041501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111972 | ACAACAAAAGCATGG[A/G]GGTATCGCTCCCAGG | 672 |
rs182070451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098201 | AGCTAATTTAAAAAA[G/T]AAATTTTTTTGTAGA | 672 |
rs182218567 | snp | A/G | 0.000173989 | 0.00932545 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044386 | CTTCACTGCCCTTGC[A/G]CACTGGGGGGGCTAG | 672 |
rs182249140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053615 | GAGCTGGTAGTGAGC[C/T]GAGACGGCGCCACTG | 672 |
rs182250051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122981 | AGAATGGCATGAACC[C/T]GGGAGGCAGAGTTTG | 672 |
rs182299673 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125607 | ATTCTACCTGAGTTT[C/G]CCATAAAGTGCCTGC | 672 |
rs182311956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052695 | TCAAAGAGACTGCGA[C/T]AGAGAAAAAAATCAG | 672 |
rs182328567 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085569 | ACATGACAACTTTAC[A/G]TTTCCTGGGAATTCC | 672 |
rs182337266 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104503 | TGTTTTCTACCTTAA[C/T]ACTAAGAAATTTGCC | 672 |
rs182377287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117969 | GCTCATATTCTAGTG[C/T]GGTAGACAGTTGATA | 672 |
rs182490553 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115075 | AATGCATAAGGATAT[A/G]CAGAAATGAACAGAA | 672 |
rs182512548 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073104 | TGGGAGGCCAAGGTA[C/G]GAAGATTGCATGAGG | 672 |
rs182514679 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054586 | CTGGGAATACAAGAG[C/T]GTGCTACGACACCCA | 672 |
rs182516793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073828 | GGTGTGATCTTGGCT[C/T]ACCGCAACCTCCGCC | 672 |
rs182524124 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095590 | CCATCTCAAAAAAAA[A/C]CAAACAAACAAACAA | 672 |
rs182572487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103038 | AGCCTCCCAAAGGGT[C/T]GGGATTATAGGCATG | 672 |
rs182603028 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113817 | GCCAGGCGCGGTGGC[C/T]TACACCTGTAATCCC | 672 |
rs182621689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099418 | TGGGATTACAGTTAT[A/G]TGCCACCACACCTGG | 672 |
rs182629224 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073762 | TGTATATATATATAT[A/G]TATATTTTTTGAGAT | 672 |
rs182630047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118971 | GGGTTTCACCATATT[A/G]CCCAGGCTGGTCTTG | 672 |
rs182653629 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077808 | GCATGATCTTGGCTC[A/G]CCACAACCTCTCTGC | 672 |
rs182657324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049715 | GCAGGGAAAGGCTAC[A/T]TGCTGAGCTGGAATC | 672 |
rs182691223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109381 | GGATCCAGAATTGGA[A/T]TGTAGCAAAGCCCAC | 672 |
rs182790231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065065 | TCGATCTCCTGACCT[C/T]GTGATCTGCCCGCCT | 672 |
rs182882946 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065792 | TCTGCGTCCTCCATG[C/T]ACTCGTCTGCTTTCT | 672 |
rs182962125 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051891 | CTGCCTGTCTTGGCC[C/T]TCCAAAGTGCTGGGA | 672 |
rs182981347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103340 | GGTCTGGTGTCGTAC[A/C]CCTGTAGTCCCAACT | 672 |
rs183112614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048494 | ACAGGCGTGAGCCAC[C/T]GCACCTAGCTTTTCT | 672 |
rs183119644 | snp | A/C | 1.64887e-05 | 0.00287125 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092021 | AGCAGAACTTTCCTT[A/C]ATGTCATTTTCAGCA | 672 |
rs183256264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083312 | AGGTGCTTGCCAAGA[C/T]GCCCGGCTAATTTTG | 672 |
rs183331660 | snp | C/T | 0.000367377 | 0.0135482 | intron-variant, missense | BRCA1 | GRCh38.p7 | 17:43079334 | AAAGAGGAGAGGCAC[C/T]TGATATATGTTCTCT | 672 |
rs183336497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101152 | CTTCCTTTTTAGCTC[C/T]ATATCTTTTGAAAAA | 672 |
rs183364842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108925 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTAAAC | 672 |
rs183369379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062512 | CTTTTATAAAACTCC[C/T]TTTCCTTTCTCTTTT | 672 |
rs183380638 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070602 | GGAGAAAAAGATGCC[G/T]TCTGGGGAATAAAAC | 672 |
rs183477289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119076 | TGAATTTTTGAAACG[A/G]ATTTTTTGGATAAAG | 672 |
rs183489787 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084231 | GAAATGGTGTTTCAC[C/T]GTGTTAGCCAGGATG | 672 |
rs183503480 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078235 | ATTATAGGTGCCCAC[C/T]ACCACCCCTTGGCTA | 672 |
rs183504832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103754 | AATCTATGAGCATCT[A/G]GCACATTCACTAACA | 672 |
rs183529484 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065110 | GCTGGGATTACAGGC[C/G]TGAGCCACCACGCTT | 672 |
rs183557525 | snp | G/T | 1.75919e-05 | 0.00296574 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115753 | TGGTCACACTTTGTG[G/T]AGACAGGTTCCTTGA | 672 |
rs183652887 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120735 | GCGCCACTGCACTCC[A/G]GCCTGGGTGAAAGAG | 672 |
rs183682289 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079599 | TTAAACACTCTAAGA[G/T]CCAAGACAGCTTCCT | 672 |
rs183687540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051579 | AAGTACTCACTATGA[A/C]CCCATCAACAGAGGG | 672 |
rs183687593 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102132 | CTGGATCGCAGTGGC[A/G]GGATCTCGGCTCACT | 672 |
rs183687995 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072249 | AAAAAATTAGCCGGG[C/T]GTGGTGGTGCATGCC | 672 |
rs183779673 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074829 | GGGAGGCTGAGGCAG[A/G]AAAATTGCTTGAACC | 672 |
rs183831660 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056737 | ACCCCAGTGAAGTGA[A/G]AAGAGCAAAGTCTTT | 672 |
rs183841852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068632 | CGATTCCCTAAGATC[A/G]TTTCTTTGCATAGTG | 672 |
rs184023162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119881 | GTAAACACAAACTTT[C/G]AACAGATGAAAACTC | 672 |
rs184094787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075641 | GGTCCCAGCTCACTG[A/C]AACCTCTGCCTCCCA | 672 |
rs184107364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097519 | GCACTTGAGGAGGCC[G/T]AGATGGGTGGATTAT | 672 |
rs184113374 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116676 | GGCGTGCGCCACCAC[A/G]CCCGGCTGATTTTTC | 672 |
rs184213765 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106193 | ACAATGGGGGCACGG[C/T]GATACAGCCCTACTT | 672 |
rs184220023 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126654 | GGAGAGTTGGAGAGT[C/T]TGTGGTTCAGAATGC | 672 |
rs184234488 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067294 | GGAGCCTTGCTCTGT[C/T]GCCAGGCTGGAATGC | 672 |
rs184237074 | snp | C/T | 0.0301816 | 0.119079 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044351 | ACAACATTTACAAAA[C/T]GTATTTTGTACAATC | 672 |
rs184247228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086900 | TACAGAGTGGGGAGT[C/T]ATCTCAAAGGTTTCT | 672 |
rs184336950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109867 | CAGTGGAACTAGATA[C/T]GCAAAAATCAACCAA | 672 |
rs184359331 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050569 | AGTGAGCCGAGATCG[C/T]GCCATTGCACTCTGG | 672 |
rs184371342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088125 | ACTAAAAGAATATAC[A/G]CCAATAAATTGCTAA | 672 |
rs184372626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071244 | GGGGTTCCCTCTGAA[A/G]GGAATGGGAGAAGTT | 672 |
rs184374817 | snp | A/C/T | 3.29545e-05 | 0.00405911 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092887 | CAGAGAATGTTGCAC[A/C/T]TTCCTCTTCTGCATT | 672 |
rs184482532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097149 | GAACCTAAAATAAAA[G/T]TTAAAATATTTTTAA | 672 |
rs184664249 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106368 | TTTTTCTGATGAATG[A/G]TTTTATAGGAACGCT | 672 |
rs184698550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066652 | CTGACCTTGTGATCT[C/G]CCCGCCTCAGGCTCC | 672 |
rs184726260 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104805 | ATAGAAAGTAATTGT[A/G]CAAACTTCCTGAGTT | 672 |
rs184820044 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125837 | CCAGCATGCGTTGCG[A/G]AATGAAAGGTCTTCG | 672 |
rs184853424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085908 | ACTATTTCTAATGTT[C/T]CTACTACTACATAAT | 672 |
rs184875949 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044122 | AGACTTCTGACCTTG[C/T]AACAATTTGTTTTGG | 672 |
rs184910839 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103254 | GGTGGATCACCTGAG[A/G]TCAGGAGTTCGAGAC | 672 |
rs184922309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124530 | CTTTCCCAGTGACCT[C/G]CTCTCATCTCTGGAT | 672 |
rs185052954 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096433 | GTCAATTAACCGGGC[A/C/G]TGGTGGTGTATACCT | 672 |
rs185186295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080311 | AACTAGGCCAGGCAC[C/T]GTAGCTCCCAAGTAG | 672 |
rs185224768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118002 | GAATTAAAGAATACA[C/T]GGGAATAAGTGCATT | 672 |
rs185244474 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059936 | TTTGAGACGGAGTCT[C/T]GCTCTTTCGCCCAGC | 672 |
rs185261284 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077258 | AATCTTAAATAATAC[A/G]TGGAACTAATGATGA | 672 |
rs185266203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098760 | CAATCCTTCTGCCTC[A/G]GTCTTCCAAAGCGTT | 672 |
rs185288076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064222 | CACCCATCTTCTAGA[C/T]GCCAAGGCTAGCTAT | 672 |
rs185304431 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102837 | TAAAAAAACTTTTAA[C/T]ATAGACAAGGACTTG | 672 |
rs185348383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121168 | ATCACAAGGTCAGGA[A/G]ATCGAGACCATCTTG | 672 |
rs185494719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110245 | ATAAAGGTTGTTAAC[G/T]AAACTTAAAAGAAAA | 672 |
rs185520356 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071637 | TAAATGTTGATGTAC[A/C]ATAAAACAGAAATGT | 672 |
rs185552909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099469 | ACAGACAGAGTTTCT[C/T]CATGTTGGCTAGGCT | 672 |
rs185558851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119033 | GACCGGGATTACAGG[C/T]GTGAGCCACTACACT | 672 |
rs185638081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047074 | GGAATTACTGGGATT[A/C]TTTTATTGTTTTTGT | 672 |
rs185646848 | snp | A/C/G | 3.32592e-05 | 0.00407783 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051139 | GAAGAGAGGAAGAGA[A/C/G]AGGGACAGGGGAATG | 672 |
rs185659604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056213 | GATCTTCTGTCTGTC[A/G]TCTAGGCTGGAGTGC | 672 |
rs185891731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113909 | TGAAAACCCTGTCTC[A/G]ACTAAAAATACAAAA | 672 |
rs185926119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068465 | CCTATAATCCCAGCA[C/T]TTTGGGAAGCTGAGG | 672 |
rs185935116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091255 | AGTCAAAGATGACGT[C/T]CTAGCTGTGTGAAGG | 672 |
rs185939239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108175 | AAACCCTGTCTCTAC[C/T]AAATATTCAAAAATT | 672 |
rs185966495 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044608 | GAAATATTCATGCCA[C/G]AGGTCTTATATTTTA | 672 |
rs186100538 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067445 | TTTTTTAGTAGAGAC[A/C/G]GGGTTTCACCATGCT | 672 |
rs186118010 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052042 | TTTTAATCTAGAAGT[A/G]AAGCCAGGTTCTGCC | 672 |
rs186161056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103104 | TTAAAAATATCAGTG[A/G]CCTTATGGCTATTTT | 672 |
rs186169069 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123108 | TGGTGGTGCACACCT[A/G]TCGTCCCTGCTACTC | 672 |
rs186194733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064450 | CTAATATTCCCCTGA[A/G]AGGGATGGGAGAATA | 672 |
rs186198860 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081840 | ATTTTTTTTGATAAC[C/T]GTAACATTGCTATAA | 672 |
rs186267814 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072667 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 672 |
rs186268206 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106865 | TAATCAAATATAAAC[A/G]GTAAGTAGTTCATGT | 672 |
rs186274125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077831 | CTCTCTGCCTCCCAG[A/G]TTCAAGCTGTTCTCC | 672 |
rs186274774 | snp | C/T | 1.65083e-05 | 0.00287296 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094703 | GCTGGCATGAGTATT[C/T]GTGCCACATGGCTCC | 672 |
rs186283015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111691 | GCTGGGCGTGGTGGC[A/G]GGCGTCTGTAGTCCC | 672 |
rs186304766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067740 | TGAGTTACCTCTAGC[A/T]CACAGCTCAGAATAC | 672 |
rs186416570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089371 | ATGATGAAGATGATA[C/T]TCATTTTTAGACGTT | 672 |
rs186421008 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060751 | ACCTCAAGTGATTTG[C/T]CTGCCTTGGCTTCCC | 672 |
rs186482467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053777 | GAGTTCAAGACCAGC[A/G]TGACCAACATGGAGA | 672 |
rs186509495 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095066 | CACTTAGGATCCATT[A/C]AATTTTTAATTTCAG | 672 |
rs186594388 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059516 | CAACAACAACAACAA[A/C]TTCTCACATCTAAAA | 672 |
rs186610614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098465 | CCTGGTTCAAGCGAT[G/T]CTCCTGCCTCAGCCT | 672 |
rs186775935 | snp | A/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125629 | AGTGCCTGCCCTCTA[A/G/T]CCTCTACTCTTCCAG | 672 |
rs186793292 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117718 | TACTCCAACCTGGGC[A/G]ACAGAGCTGGACTCC | 672 |
rs186832985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076384 | GTGTATAAATGCCTG[C/T]ATGCAAAAAACTGGA | 672 |
rs186914333 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079472 | GCCCCACAAGTGTTA[A/C]CATGGCAAAACTGGA | 672 |
rs186933566 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083440 | GGATTAGAGACATGC[A/G]CCATTGTGCCTGACC | 672 |
rs186936074 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119976 | AATGTTCCCCTTCTA[C/G]GTCCTGATGAGAGTA | 672 |
rs186949625 | snp | G/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124747 | CATACCAGCCGGTGT[G/T]TTTTGTTTTGTTTTG | 672 |
rs186955850 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062603 | GTTTGCGCTGCAAAA[A/T]TTTTTTTTTTTTTAA | 672 |
rs187084458 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049950 | ATACTTTCTGGCAAC[C/T]CTGGTTTCCACTATA | 672 |
rs187085958 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070790 | TCAGAAATTAGTAAT[C/T]GAAATTAAATTACAC | 672 |
rs187106682 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073221 | CAATTTGGGGGCAAT[A/G]AGCTTATAGCAATTT | 672 |
rs187132948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103421 | GCAGTGAGCTGACAT[C/T]GTGTCACTGCGCTCC | 672 |
rs187218638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071351 | TTAAGAGAAAAATGG[C/G]TACATGAATACAGTG | 672 |
rs187294938 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112322 | CGAACTCCTGACCTC[A/G]TGATCCGCCCACCTC | 672 |
rs187334602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052916 | CAGTCTTGCACTGTC[A/G]CCTGGGCTGGAGTGC | 672 |
rs187354131 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109923 | TTTTTTAGACGGAGT[C/T]TCGCTCTGTCTCTCA | 672 |
rs187433304 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066131 | TTGTGTTAATACGGC[C/T]CAGTTTCAAATAAGC | 672 |
rs187446698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104596 | GTATCACTAAGAAAG[A/C]AAGCACACAAATTAA | 672 |
rs187482044 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095598 | AAAAAAAACAAACAA[A/T]CAAACAAAAAAAAAA | 672 |
rs187487187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115548 | ACTTTACCAGGAACT[A/G]TGATTACAACCAACT | 672 |
rs187507971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073142 | TTAGAGACCAGCCTC[A/G]GCAACATAACAAGAC | 672 |
rs187514483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073858 | CTCCCGGGTTCAAGT[G/T]ATTCTGCTGCCTCAG | 672 |
rs187676042 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054684 | GGGCTCAAGTGATCC[A/T]CCTGCCTTGGCCTCC | 672 |
rs187689327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085750 | GGCTAATTCTAATAA[C/G]ACTCCTGAAATGTGC | 672 |
rs187817658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065375 | TGTATCTCTGTGAAA[A/T]GAATCATCATAGGCT | 672 |
rs187977357 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084667 | TTCAGGAGGTTTTTA[C/T]GACCAGAAAATGTAT | 672 |
rs187992882 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125347 | CCACAGCCTGTCCCC[A/C]GTCCAGGAAGTCTCA | 672 |
rs188018039 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069408 | GTTTAAAGACAACAT[A/G]TACCCAAGCCACTTG | 672 |
rs188030827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109515 | CTTGGGTCCTTCTTC[A/G]CCGATATAGATGCTT | 672 |
rs188039922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109265 | GCATCCCAACGTGCT[C/G]GGATTACAGGCATGA | 672 |
rs188101457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056880 | AAAGTAGAGACAATA[C/T]TTATTTATGTGGTTG | 672 |
rs188215342 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061739 | AGGCACATGCCACCA[A/C]GCTCGACTAATTTTT | 672 |
rs188268795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075472 | GAGGTTAATTAATTT[A/G]AACAATTATTGGGTG | 672 |
rs188273106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097189 | AACATCAATCCTTAA[C/T]ATTAACTAAATAGGA | 672 |
rs188280742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115969 | AGCAGAGAATACGAT[C/T]CTTACCTTCAGTGAG | 672 |
rs188479441 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119341 | TATTGTGAAGGGTTG[G/T]AATACAACTCTTGTA | 672 |
rs188507721 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078477 | ATGCCTGGCCAAGGC[A/G]GAAATATTTAATAAG | 672 |
rs188534348 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054622 | TTTTTAAATTTTTTT[A/G]TAGAGACAGGGTCTT | 672 |
rs188704587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120759 | GAAAGAGCGAGACTC[C/T]GTCTCAAAAACAAAA | 672 |
rs188719262 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111432 | GGCTGAGGCAGGAGA[A/T]TTGCTTGAACCCAGG | 672 |
rs188741493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051700 | GGAGCGTAGTGGTGC[A/G]ATCTGGGCTCACTGC | 672 |
rs188745801 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072337 | GAGGTTGCGCTGAGC[C/T]GAGATTGCGCCATTG | 672 |
rs188760624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105332 | GCAGCCTCAGACTTC[C/T]GTACTCAAGCTATCC | 672 |
rs188840263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115892 | TTATGACTGAGTCAA[A/C]ATAAGGCCTCAAGTT | 672 |
rs188913488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064254 | GATCTCCATTATAGT[A/G]TTCAAGGAATTAGGA | 672 |
rs189070826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066893 | TGCGATCTTGGGTCA[C/T]TGCAACCTCCACCTC | 672 |
rs189101336 | snp | C/T | | | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044207 | AGATACTATCATTAC[C/T]CCCATTTTACAGAGT | 672 |
rs189108346 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096544 | GCCACTACACTCCAT[C/G]CTGGCAACAGGGCAA | 672 |
rs189133089 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106759 | GAAAACTGAACTTAC[A/T]TGCATATGGCTTACT | 672 |
rs189148733 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056399 | GCCCAGGCTGGTATC[A/C/G]AACTCCTTGGCTCAA | 672 |
rs189160627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067489 | TCGATCTCCTAATCT[C/T]GTGATCTGCCCGCCT | 672 |
rs189187763 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097747 | AAAATAAGTATAATA[A/G]GAACAATCTCAGAGG | 672 |
rs189193276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117562 | TGGCCAACACAGTGA[A/G]ACGCTGTCTCTACTA | 672 |
rs189206737 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103105 | TAAAAATATCAGTGA[C/T]CTTATGGCTATTTTA | 672 |
rs189216545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123821 | AAAGGAGAGGAGTGG[G/T]AGAGGCAGAGTGGAT | 672 |
rs189304636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051279 | CTGCTACTTCCCAGG[A/G]ACAAGCAGTCCAATG | 672 |
rs189352191 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106203 | CACGGCGATACAGCC[C/T]TACTTTACATAAGTC | 672 |
rs189361338 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127154 | CGACGGGCACCGCCC[C/G]CTGCTCCTCAGCGCC | 672 |
rs189382442 | snp | C/T | 0.000361991 | 0.0134486 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044355 | CATTTACAAAACGTA[C/T]TTTGTACAATCAAGT | 672 |
rs189390399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067348 | CAACCTCCATCTCCC[C/G]GGTTCAAGTGATTCT | 672 |
rs189411010 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089147 | GTGAAACCCTCTCTC[A/T]ACTAAAAAAATACAA | 672 |
rs189442183 | snp | A/C/G/T | 0.000639855 | 0.0178758 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43045572 | ATATTTAGTAGCCAG[A/C/G/T]ACAGTAGAAGGACTG | 672 |
rs189568702 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110407 | CCTGGGAAACATGGC[A/G]AAACCCCGTCTCTAC | 672 |
rs189602222 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071885 | TGGTGGCGGGCGCCT[A/G]TAGTCCCGGCTACTA | 672 |
rs189643446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079616 | CAAGACAGCTTCCTG[A/G]AACGCGTGAAGGAAA | 672 |
rs189644056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099311 | GTTTCGCTATTTTTG[C/T]CCAGGCTGGAGTGCA | 672 |
rs189649477 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118502 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAA | 672 |
rs189676688 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060047 | AGTAGCTGTGATTAC[A/G]GGCACATGCCACCAT | 672 |
rs189678812 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077625 | AGACATGAGCCACTG[C/G/T]GCCCAGCCTAATTCA | 672 |
rs189898944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063644 | TCATATGCTAACATT[A/G]CTAGGAGCAGATTAG | 672 |
rs189910357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102440 | CGGCTCACTGCAACC[A/T]CCGACTCTCAGGTTC | 672 |
rs189973036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119074 | TGTGAATTTTTGAAA[C/T]GGATTTTTTGGATAA | 672 |
rs189986725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103002 | TGTTGCCCAAGCTGG[C/G]CTCAAAGGACCTCCT | 672 |
rs190107337 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054583 | TAGCTGGGAATACAA[A/G]AGTGTGCTACGACAC | 672 |
rs190123841 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073768 | TATATATATATATAT[A/T]TTTTGAGATGGAGTC | 672 |
rs190124246 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089452 | TTCATATTACATTAT[A/C]AAATGGTCATATATA | 672 |
rs190126659 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086012 | GTGAATATTTTCAAA[C/T]ATACAGAAAACTTGA | 672 |
rs190128845 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095441 | CAAAAAATTAACCGG[A/C/G]TGTGGTGGCATGCGC | 672 |
rs190133561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058655 | TTAGACTGCTAATAC[C/T]GTGCTGTTATAAAGG | 672 |
rs190198082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121762 | AAGCTAGAAAACATA[A/G]TAGTTGATTGAAAAT | 672 |
rs190232876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081537 | GATAAGAATCACTGA[A/G]CTAGGAATGAAGTGT | 672 |
rs190285961 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114406 | TTTTTTTTTTTTTTT[G/T]GAGTCTCCCTCTTGT | 672 |
rs190347228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075830 | ATCTCTGAAAGATAT[C/T]CTAAATGTTTTCTGG | 672 |
rs190387252 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117726 | CCTGGGCGACAGAGC[C/T]GGACTCCATCTCAAA | 672 |
rs190562999 | snp | A/G/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084092 | CTGGAGTGCAGTGGC[A/G/T]CAATCTTGGTTCACT | 672 |
rs190610767 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111801 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 672 |
rs190680683 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098540 | ATTTTTTTTTTTTTT[C/T]GTATTTTTAGTAAAG | 672 |
rs190716334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070280 | TGACAATTAATTACA[C/G]GGGTGGTAAACTTCT | 672 |
rs190731172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109294 | GAGCCATCAAGCCTG[A/G]CCTTATCTTCATTTT | 672 |
rs190756329 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068330 | GTTTAATAAAAATTA[C/T]GTACACATCAGCAGA | 672 |
rs190861568 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125374 | CTCAGCGAGCTCACG[A/C]CGCGCAGTCGCAGTT | 672 |
rs190900046 | snp | A/C | 3.29468e-05 | 0.00405861 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43104197 | ACTTTGGATGATAGA[A/C]ACTTCATCTTTTAGA | 672 |
rs191000183 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049594 | GGTAACTGATAATCA[C/T]GGCCACTGAAAATAC | 672 |
rs191034650 | snp | C/T | 9.92113e-05 | 0.00704243 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099745 | ATCCAGCAATTATTA[C/T]TAAATACTTAAAAAA | 672 |
rs191039222 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068528 | CCAAGACCAGCCTGG[C/G]CAATACAGTGAGATT | 672 |
rs191056374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108484 | GAGGCAGGCAGATCA[C/G]TTGAGGCCTGGAGTT | 672 |
rs191073269 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061302 | CTGGCCTCCTTAAAC[A/G]AAAGTAATCAACAAC | 672 |
rs191197821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124548 | CTCATCTCTGGATCC[C/T]CCTCAAGCACATCCC | 672 |
rs191230495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082898 | CATTTAAACACTATC[A/G]ATATTTAAAATTAGC | 672 |
rs191311966 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107288 | CAGGATGGTCTCCAT[C/G]TCCTGACCTCGTGAT | 672 |
rs191322344 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43078030 | GTGAGCCACTGCGCC[C/T]GACCGTTATTTTTCA | 672 |
rs191331108 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079473 | CCCCACAAGTGTTAC[C/T]ATGGCAAAACTGGAA | 672 |
rs191341657 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101767 | TCAGCCTCCCGAAGT[G/T]CTGGGATTACAGGTG | 672 |
rs191351866 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120355 | CAGTCATGATCATTC[C/G]TGATCACATATTAAG | 672 |
rs191373374 | snp | C/T | 6.65901e-05 | 0.0057698 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43063351 | ATTCAGCATTTTTCT[C/T]TCTTTAATAGACTGG | 672 |
rs191431246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103339 | AGGTCTGGTGTCGTA[C/T]CCCTGTAGTCCCAAC | 672 |
rs191463425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065040 | TTTCACCGTGTTAGC[C/T]AGGATGGTCTCGATC | 672 |
rs191509111 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109673 | CTACAAATACTACAT[A/G]TACTCTAGTATAATG | 672 |
rs191514351 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103431 | GACATCGTGTCACTG[C/T]GCTCCAGCCTGGGCG | 672 |
rs191530610 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050473 | AAAAAATTAGTCGGG[C/T]GTGGTGGCACACGCC | 672 |
rs191530878 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072939 | CCAGGCTGGTCTTGA[A/T]CTCTTGGCCTCGAGC | 672 |
rs191784032 | snp | A/C | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125050 | CCTATCACGAGGATT[A/C]CCCCACGGACACTCA | 672 |
rs191850318 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052675 | GGCCTAAAATTCACC[C/T]GGCTTCAAAGAGACT | 672 |
rs191863976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053522 | AAAAAATTAGCTGGG[C/T]ATGGTGGCGGGCACC | 672 |
rs191872612 | snp | A/T | 2.18195e-05 | 0.00330292 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43094848 | ACATCCGTCTCAGAA[A/T]ATTCACAAGCAGCTG | 672 |
rs191994609 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048617 | CCTCCCACGTTCAAG[C/T]GATGCTCACACCTCA | 672 |
rs191995002 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044261 | GGCTCTGAGAAAGTC[A/G]GCTGGCCTAAGTCTC | 672 |
rs191995326 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067172 | AAGCAGCAAAACTAT[C/T]ATTTGTCTTTCATAA | 672 |
rs191998879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115611 | AAATGGAGTTGGATT[C/T]TTCGTTCTCACTTAA | 672 |
rs192003724 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086755 | TGATGGGTATATTGA[C/T]AGAGTCCCAAACCCA | 672 |
rs192139502 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113603 | TAATTTCCTGACCTC[A/G]TGATCCGCCCACCTC | 672 |
rs192171607 | snp | A/C | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105501 | CCACCTCAGCCTCCT[A/C]GAGTGCTAGGGTTAT | 672 |
rs192172777 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073240 | TTATAGCAATTTTGT[A/T]AGAAAGGAAAAAAAA | 672 |
rs192322420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059763 | ATCTCCACACCACCA[A/G]TTACCACAAGGATAA | 672 |
rs192405369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084706 | TCACAAAGGTTTCTA[C/T]TGCTACTCTAACACT | 672 |
rs192408582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056661 | CTGGGCAATGGAGTG[A/G]GACTCCGTCTTGGGA | 672 |
rs192436157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065589 | GAATCGCTTGAACCC[A/G]GGAGGGGGAGGTTGC | 672 |
rs192528708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061987 | ACTCTATCTTATTTA[C/T]TTCTCACTGTTCTCA | 672 |
rs192554410 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062289 | TTGTGGAGACAGAGT[C/T]TCACTATGTTGCCCA | 672 |
rs192567152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102644 | GCAGGTGTTAGCCGC[C/T]GCACCCAGCCAGTTC | 672 |
rs192655097 | snp | C/G | 1.64814e-05 | 0.00287061 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43093075 | TTTCTATTATCTTTG[C/G]AACAACCATGAATTA | 672 |
rs192658149 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110175 | CTGGGATTACAGGCG[C/T]GAGCCACCGCACCCG | 672 |
rs192782245 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125799 | ATAAGGATTGTTGGG[C/G]GGGTGGAGGGAAATA | 672 |
rs192800327 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085860 | TATATATATAAAACC[C/T]TCCCATAAAACATGT | 672 |
rs192816557 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120810 | GCCAGGCGCAGTGGC[C/T]CACGCCAGCACTTTG | 672 |
rs192830629 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079887 | TTCTTACTACAATGG[C/G]CCTCATGCAATGAAG | 672 |
rs192877587 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074090 | GTACACCAAGACTCC[C/T]TCATCCTCAAAATCA | 672 |
rs193011029 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104599 | TCACTAAGAAAGAAA[A/G]CACACAAATTAAACA | 672 |
rs193017953 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096768 | ATTACTGCTGTGTCA[A/C/G]TATTACTGTATATGA | 672 |
rs193059967 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096246 | GCCGGGTGTGGTGGC[A/G]CGCGCCTGTAGTCCC | 672 |
rs193076298 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056200 | TTTTTTCTTTTGAGA[A/T]CTTCTGTCTGTCGTC | 672 |
rs193146830 | snp | C/G | 0.000147118 | 0.0085754 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079330 | AGGGAAAGAGGAGAG[C/G]CACCTGATATATGTT | 672 |
rs193149108 | snp | A/G | 0.000132996 | 0.00815356 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051137 | AAGAAGAGAGGAAGA[A/G]AGAGGGACAGGGGAA | 672 |
rs193150833 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119569 | CTTGGGAAAATGCTT[C/G]ACAACCTGAGATGAC | 672 |
rs193175876 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126133 | CGGGGACGCAGTGAG[A/C/T]GCCGAATTTGCCTGG | 672 |
rs193214469 | snp | C/T | 0.000399281 | 0.0141238 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43115929 | ATATTTATTAAATGT[C/T]TGCTGTGTCAGGAAC | 672 |
rs193221861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074594 | TACTTGCTGGGCAGC[C/T]AAAGCATAAATGAAA | 672 |
rs193299759 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101016 | GATTACAGCCATGAG[A/C/G]CACCGTGCCTGGCCA | 672 |
rs193299888 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071480 | AGTTTTAGAAATATA[A/T]CCTAGGGAGATAAAA | 672 |
rs199522616 | snp | A/G | 1.68035e-05 | 0.00289853 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106492 | CATAAAGGACACTGT[A/G]AAGGCCCTTTCTTCT | 672 |
rs199527524 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057148 | ATGCTGAAAGAAACC[A/G]AACACAACCCATCAG | 672 |
rs199540030 | snp | C/T | 9.88647e-05 | 0.00703012 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094134 | AGGCTTGCCTTCTTC[C/T]GATAGGTTTTCCCAA | 672 |
rs199689700 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125993 | ATGGACTGGAGTGTT[C/T]TGTTTTCGTATTTTG | 672 |
rs199805151 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124158 | ACCAGATGGGACACT[-/CT]AAGATTTTCTGCATA | 672 |
rs199835679 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123325 | TTCCAAATACCTATC[C/T]TCTCAACGACACCGA | 672 |
rs199839105 | in-del | -/G | 0.411578 | 0.190768 | BRCA1 | 17 | allele_origin=G(germline)/(germline) | 17:43122889 | GCCTCTACTAAAAAA[-/G]AAAAAAAAATACAAA | 672 |
rs199858368 | snp | A/G | 1.66551e-05 | 0.00288571 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051148 | AAGAGAGAGGGACAG[A/G]GGAATGGAGAGAAGG | 672 |
rs199916228 | snp | C/T | 9.64348e-05 | 0.00694321 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43095830 | TGCCTGTTAAGTTGG[C/T]AAACTTTGCCATTAC | 672 |
rs199954851 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092793 | TTGATATTAGACTCA[C/T]TCTTTCCTTGATTTT | 672 |
rs200081820 | in-del | -/T | 0.00835141 | 0.0640778 | BRCA1 | 17 | allele_origin=T(germline)/(germline) | 17:43098205 | AATTTAAAAAAGAAA[-/T]TTTTTTGTAGAGATG | 672 |
rs200083681 | in-del | -/AT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100609 | TTATATATATATAAC[-/AT]ATATATATAACATAT | 672 |
rs200098203 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090064 | GAAAAAAAAAAAGAA[-/G]AAGAGAAAGAAGTAT | 672 |
rs200147389 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080890 | TCCCTGTCTCTACTT[-/A]AAAAAAAAAATTAAA | 672 |
rs200178928 | in-del | -/AA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096572 | CAAGACCCCGTCTCC[-/AA]AAAAAAAAAAAAAAA | 672 |
rs200197396 | in-del | -/AAAGAAAAAAAAAAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104067 | CATCTCAAAAAAAAA[-/AAAGAAAAAAAAAAG]AAAAGAAGAAGAAGA | 672 |
rs200225694 | in-del | -/TC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048507 | ACCGCACCTAGCTTT[-/TC]TCTCTCTCTCTTTTT | 672 |
rs200358748 | snp | C/T | 1.64917e-05 | 0.00287151 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104117 | AAGAAAACAAATGGT[C/T]TTACCAAGGAAGGAT | 672 |
rs200368134 | in-del | -/TAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095103 | CCTATGCAGAAACCA[-/TAC]CACCTATTTCTCTAA | 672 |
rs200393646 | snp | C/T | 0.00019818 | 0.00995242 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076662 | ACTGCTTTGTTCTGA[C/T]AGTGATAATTCAGGT | 672 |
rs200407477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051041 | CTGGTGCTGGAACTC[C/T]GGGGTTCTCCCAGGC | 672 |
rs200424092 | in-del | -/T | 0.0345262 | 0.126772 | BRCA1 | 17 | allele_origin=T(germline)/(germline) | 17:43072015 | TCCGTCTCAAAAAAA[-/T]AAATAAATAAAAATA | 672 |
rs200432771 | snp | A/C/T | 0.00199792 | 0.0315431 | BRCA1 | 17 | allele_origin=T(inherited)/A(inherited)/C(germline) | 17:43071011 | TCAATTCTGGCTTCT[A/C/T]CCTGCTCACACTTTC | 672 |
rs200449040 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104150 | TCGGGTTCACTCTGT[A/G]GAAGTCTTTTGGCAC | 672 |
rs200489356 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048519 | TTTCTCTCTCTCTCT[-/C]TTTTTTTTTTTTTTA | 672 |
rs200513210 | snp | A/G | 0.000200578 | 0.0100124 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123969 | TGTTCATTTGCATAG[A/G]AGATAATCATAGGAA | 672 |
rs200521980 | snp | C/T | 4.94466e-05 | 0.00497201 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093314 | AGCATTATTAGACAC[C/T]TTAACTGTTTCTAGT | 672 |
rs200571203 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067321 | ATGCAGTGGCATGAT[C/T]TCGGCTCACTGCAAC | 672 |
rs200582930 | snp | A/G | 0.00199806 | 0.0315443 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43076558 | ACTTGTCAGCAGAAA[A/G]GCCTTCTGGATTCTG | 672 |
rs200599235 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057143 | AAATCATGCTGAAAG[A/G]AACCAAACACAACCC | 672 |
rs200616937 | snp | A/G | 4.95577e-05 | 0.00497759 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094007 | ATGAAGGCCTGATGT[A/G]GGTCTCCTTTTACGC | 672 |
rs200639029 | in-del | -/AT | 0.359998 | 0.2245 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100574 | ATATATATATATAAC[-/AT]ATATATATAACATAT | 672 |
rs200648498 | snp | A/C/G/T | 0.000399281 | 0.0141238 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43091733 | ACTGCAGTCATTTAA[A/C/G/T]CTATTCTTCAATGAT | 672 |
rs200692583 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123326 | TCCAAATACCTATCC[C/T]CTCAACGACACCGAT | 672 |
rs200774622 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43061102 | CTGCACTCCAGCCTG[G/T]GGGATAGAGGGAGAC | 672 |
rs200781379 | in-del | -/AAG | 0.456685 | 0.140646 | BRCA1 | 17 | allele_origin=G(germline)/(germline) | 17:43090059 | AAAGGGAAAAAAAAA[-/AAG]AAGAAGAGAAAGAAG | 672 |
rs200991398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099890 | TTCCTGCTAAACAGT[A/G]TGGTAAAGAACAGTC | 672 |
rs201060127 | in-del | -/AC | 0.0189856 | 0.0955633 | BRCA1 | 17 | allele_origin=C(germline)/(germline) | 17:43099410 | CGAGTAGCTGGGATT[-/AC]AGTTATGTGCCACCA | 672 |
rs201117483 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075565 | ACTGCTCTCTCTCTC[C/T]TTTTTTTTTTGTTTT | 672 |
rs201152151 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057141 | CAAAATCATGCTGAA[A/G]GAAACCAAACACAAC | 672 |
rs201190540 | snp | A/G | 3.29723e-05 | 0.00406018 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092648 | AATGAGTCCAGTTTC[A/G]TTGCCTCTGAACTGA | 672 |
rs201196020 | snp | G/T | 0.0670526 | 0.170383 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43045691 | AGTCAGTAGTGGCTG[G/T]GGGGGATCTGGGGTA | 672 |
rs201212001 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056687 | TGGGAAAAAAAAAAA[-/G]AGAGAGAGAGAGCAA | 672 |
rs201290746 | snp | C/T | 0.00299544 | 0.0385843 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079417 | GTAAGAAAGGTGAAA[C/T]TGTAGACATCAAGGG | 672 |
rs201302829 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057822 | GCCTGGGCAACTGAG[C/T]GAGACTCCGTCTCAA | 672 |
rs201348696 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121198 | GGCTAACATGGTGAA[A/C]CCCCGTCTCTACTAA | 672 |
rs201441987 | snp | A/G | 0.000399281 | 0.0141238 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094736 | ATGCAAGTTTGAAAC[A/G]GAACTACCCTGATAC | 672 |
rs201508566 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079789 | GGCATAATAGGTGTT[-/A]AAAAAAAAAAAAAAA | 672 |
rs201515231 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065997 | CTCTCCAATTTGTCA[A/G]TGACCATGTTAAAAA | 672 |
rs201518255 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110588 | GTAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 672 |
rs201521493 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067837 | ACTATTTAAAGTGAA[A/T]TTTTTTTTTTTTTTT | 672 |
rs201536070 | snp | A/G/T | 6.60655e-05 | 0.00574703 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline) | 17:43097267 | AGTTGCCTTATTAAC[A/G/T]GTATCTTCAGAAGAA | 672 |
rs201546026 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106665 | AAAAGTAATGGCAGG[G/T]GAATTACAAGCAATA | 672 |
rs201596327 | snp | A/G | 1.73797e-05 | 0.0029478 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095890 | TCCCTGGTTCCTTGA[A/G]GGGTGATTTGTAACA | 672 |
rs201644509 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050880 | GGGGACAAGGTATAG[-/T]TTTTTTTTTGCCATA | 672 |
rs201664159 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097347 | TTAATTAAAAGGGTT[A/T]AAAAAATGTACTTGT | 672 |
rs201678971 | in-del | -/AT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100586 | TAACATATATATAAC[-/AT]ATATATATTATATAT | 672 |
rs201810810 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070971 | ACCATGGACATTCTT[C/T]TGTTGACCCTTTCTG | 672 |
rs201851352 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056681 | CCGTCTTGGGAAAAA[A/C]AAAAAGAGAGAGAGA | 672 |
rs201855886 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096141 | CAGCACTTTGGGAGG[C/T]TGAGGCGGGTGGACC | 672 |
rs201866997 | snp | A/G | 9.94342e-05 | 0.00705033 | BRCA1, NBR2 | 17 | allele_origin=G(germline)/A(germline) | 17:43124125 | AATGAACTTTAACAC[A/G]TTAGAAAAACATATA | 672 |
rs201875054 | snp | C/T | 3.29522e-05 | 0.00405894 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093236 | TGAAATACTGCTACT[C/T]TCTACAGATCTTTCA | 672 |
rs201905092 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106068 | AGGCTACAGTGAGCC[A/G]AGATCACGCCACTGC | 672 |
rs201929625 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073562 | TAAAACTCTGATTTA[A/C]AAGCCATAAAACACC | 672 |
rs201957007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066089 | TGGGGCTCTGGATCT[A/G]TACTTCACTTGCTCC | 672 |
rs201957408 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43045876 | TAATCAATCGACTCC[A/G]GGGTCCTGGTTGTAT | 672 |
rs201979969 | in-del | -/TC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089550 | AATTGTGTACTTTCT[-/TC]TTTTTTTTTTTTTTG | 672 |
rs202004680 | snp | C/T | 0.00199806 | 0.0315443 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092748 | CCAACCACAGGAAAG[C/T]CTGCAGTGATATTAA | 672 |
rs202071043 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113784 | AATCTCTCTTTTTTT[-/T]GTTAAGAGACAGGGT | 672 |
rs202101994 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118393 | ATTTTCTTTTTTTTT[C/T]TCAGACAGAGTCTCG | 672 |
rs202137181 | in-del | -/ATATATATAACATATATATATT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100575 | ATATATATATATAAC[-/ATATATATAACATATATATATT]ATATATATATAACAT | 672 |
rs202168814 | snp | C/G/T | 0.00199798 | 0.0315436 | BRCA1, NBR2 | 17 | allele_origin=G(germline)/T(germline) | 17:43124037 | GGGACACTCTAAGAT[C/G/T]TTCTGCATAGCATTA | 672 |
rs202169687 | in-del | -/CACT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052822 | ACACACACACACACA[-/CACT]CTCTTACTTTACCGC | 672 |
rs202171570 | snp | C/T | 1.68018e-05 | 0.00289838 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104293 | AAAACATTATGTTTG[C/T]AGTTAGAGAAAAATG | 672 |
rs207476411 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087917 | TTTTTTTTTTCCCAG[A/G]CAGGGGTTGCCCAGA | 672 |
rs207476412 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122668 | ATCCCAGCACCTTGA[A/G]AGGCCAAGGGAGGGT | 672 |
rs267604892 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071161 | CACGAGCTGACTCTG[A/G]GGCTCTGTCTTCAGA | 672 |
rs273897652 | in-del | CAC/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094408 | ATGTTCCTTGGATAA[CAC/T]TAAATAGCAGCATTC | 672 |
rs273897653 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094365 | AGTGGTTTTCCAGAA[-/G]TGATGAACTGTTAGG | 672 |
rs273897654 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124107 | GTTAAAGTTCATTGG[A/C]ACAGAAAGAAATGGA | 672 |
rs273897655 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094327 | GACTCACATGATGGG[G/T]AGTCTGAATCAAATG | 672 |
rs273897656 | snp | C/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094212 | ATCCTCATGAGGCTT[C/G/T]AATATGTAAAAGTGA | 672 |
rs273897657 | in-del | -/T | | | splice-donor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43115724 | CACATATTTTGCAAG[-/T]AAGTTTGAATGTGTT | 672 |
rs273897658 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094144 | GACAAAATATTTGGG[-/A]AAACCTATCGGAAGA | 672 |
rs273897659 | in-del | AA/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094141 | CAAAATATTTGGGAA[AA/G]CCTATCGGAAGAAGG | 672 |
rs273897660 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106522 | ATAGATTTTGCATGC[G/T]GAAACTTCTCAACCA | 672 |
rs273897661 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124110 | TGTGTTAAAGTTCAT[C/T]GGAACAGAAAGAAAT | 672 |
rs273897662 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106518 | ATTTTGCATGCTGAA[-/A]CTTCTCAACCAGAAG | 672 |
rs273897663 | multinucleotide-polymorphism | GC/TA | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093969 | GATTTTATCAAGAAA[GC/TA]AGATTTGGCAGTTCA | 672 |
rs273897664 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093835 | TCTATTCAGAATGAG[-/G]AAAAATCCTAACCCA | 672 |
rs273897665 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106478 | TCACAGTGTCCTTTA[-/A]TGTAAGAATGATATA | 672 |
rs273898666 | in-del | -/AT | | | splice-acceptor-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124116 | TTCTAATGTGTTAAA[-/AT]GTTCATTGGAACAGA | 672 |
rs273898667 | in-del | -/AT | 0.000527741 | 0.0162355 | BRCA1, NBR2 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43124135 | AAGATATATATATAT[-/AT]GTTTTTCTAATGTGT | 672 |
rs273898668 | in-del | -/AG | | | splice-acceptor-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124117 | TTTCTAATGTGTTAA[-/AG]AGTTCATTGGAACAG | 672 |
rs273898669 | snp | A/G | 0.000255069 | 0.0112902 | BRCA1, NBR2 | 17 | allele_origin=G(germline)/A(germline) | 17:43124118 | TTTTCTAATGTGTTA[A/G]AGTTCATTGGAACAG | 672 |
rs273898670 | in-del | -/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124169 | TAAAATGAAGTTGTC[-/T]ATTTTATAAACCTTT | 672 |
rs273898671 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124120 | GTTTTTCTAATGTGT[C/T]AAAGTTCATTGGAAC | 672 |
rs273898672 | snp | C/T | 0.000798403 | 0.0199641 | BRCA1, NBR2 | 17 | allele_origin=T(germline)/C(germline) | 17:43125260 | TAAAGGTAGTAGAGT[C/T]CCGGGAAAGGGACAG | 672 |
rs273898673 | in-del | -/A | | | frameshift-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43106464 | ATGTAAGAATGATAT[-/A]AACCAAAAGGTATAT | 672 |
rs273898674 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093472 | AACAAGCCAAATGAA[C/T]AGACAAGTAAAAGAC | 672 |
rs273898675 | snp | A/C | | | missense, intron-variant | BRCA1 | GRCh38.p7 | 17:43106462 | GTAAGAATGATATAA[A/C]CAAAAGGTATATAAT | 672 |
rs273898676 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093460 | TGAACAGACAAGTAA[-/AA]GACATGACAGCGATA | 672 |
rs273898677 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093428 | TTTCCCAGAGCTGAA[A/G]TTAACAAATGCACCT | 672 |
rs273898678 | snp | G/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093401 | ACCTGGTTCTTTTAC[G/T]AAGTGTTCAAATACC | 672 |
rs273898679 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093389 | TACTAAGTGTTCAAA[-/T]ACCAGTGAACTTAAA | 672 |
rs273898680 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093356 | ATTTGTCAATCCTAG[C/T]CTTCCAAGAGAAGAA | 672 |
rs273898681 | in-del | -/GAAAAAGAAGAGAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093330 | AGCCTTCCAAGAGAA[-/GAAAAAGAAGAGAA]ACTAGAAACAGTTAA | 672 |
rs273898682 | snp | A/T | 0.000230643 | 0.0107363 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43093245 | TTTGCAAACTGAAAG[A/T]TCTGTAGAGAGTAGC | 672 |
rs273899683 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093111 | TGAGTCAGTGTGCAG[A/C]ATTTGAAAACCCCAA | 672 |
rs273899684 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104926 | TACGAGATTTAGTCA[-/A]CTTGTTGAAGAGCTA | 672 |
rs273899685 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093041 | CACAGAAGGCTTTAA[-/AA]GTATCCATTGGGACA | 672 |
rs273899686 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093023 | ATCCATTGGGACATG[-/AA]GTTAACCACAGTCGG | 672 |
rs273899687 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092845 | TCCTTAAAGAAACAA[-/A]GTCCAAAAGTCACTT | 672 |
rs273899688 | snp | A/C/T | | | missense, synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092792 | AAATCAAGGAAAGAA[A/C/T]GAGTCTAATATCAAG | 672 |
rs273899689 | in-del | CC/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092718 | GGTCAGAAAGATAAG[CC/G]AGTTGATAATGCCAA | 672 |
rs273899690 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092632 | GAAACTGGACTCATT[A/T]CTCCAAATAAACATG | 672 |
rs273899691 | snp | A/G | 4.95372e-05 | 0.00497656 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092600 | ACTTTTACAAAACCC[A/G]TATCGTATACCACCA | 672 |
rs273899692 | multinucleotide-polymorphism | CT/TA | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092535 | TGTAAGAAAAATCTG[CT/TA]AGAGGAAAACTTTGA | 672 |
rs273899693 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124098 | CATTGGAACAGAAAG[A/T]AATGGATTTATCTGC | 672 |
rs273899694 | in-del | -/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43104865 | ACAGGTTTGGAGTGT[-/T]AAGTGTTGAATATCC | 672 |
rs273899695 | in-del | -/A | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43104263 | TCCCTTGTATTTTAC[-/A]GATGCAAACAGCTAT | 672 |
rs273899696 | snp | A/C | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092505 | AGGAACATTCAATGT[A/C]ACCTGAAAGAGAAAT | 672 |
rs273899697 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104348 | ACACAACAAAGAGCA[C/T]ACATAGGGTTTCTCT | 672 |
rs273899698 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092434 | CGTAATAACATTAGA[A/G/T]AAAATGTTTTTAAAG | 672 |
rs273899699 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092426 | CATTAGAGAAAATGT[-/T]TTTTAAAGAAGCCAG | 672 |
rs273899700 | in-del | AGCC/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092414 | AAATGTTTTTAAAGA[AGCC/GA]AGCTCAAGCAATATT | 672 |
rs273899701 | in-del | CC/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092342 | TTAATGAAATAGGTT[CC/G]AGTGATGAAAACATT | 672 |
rs273899702 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092341 | AATGAAATAGGTTCC[A/T]GTGATGAAAACATTC | 672 |
rs273899703 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092305 | GAACTAGGTAGAAAC[-/A]GAGGGCCAAAATTGA | 672 |
rs273899704 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092244 | CTGAGGTCTATAAAC[A/G]AAGTCTTCCTGGAAG | 672 |
rs273899705 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092188 | AAGCAAGAATATGAA[-/G]AAGTAGTTCAGACTG | 672 |
rs273899706 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092114 | ACAGCCTATGGGAAG[-/T]AGTCATGCATCTCAG | 672 |
rs273899707 | in-del | AAA/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092052 | AGATGATGGTGAAAT[AAA/C]GGAAGATACTAGTTT | 672 |
rs273899708 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092023 | TTTGCTGAAAATGAC[A/T]TTAAGGAAAGTTCTG | 672 |
rs273899709 | in-del | AG/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091981 | CAAAAGCGTCCAGAA[AG/T]GAGAGCTTAGCAGGA | 672 |
rs273900710 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091950 | GTCCTAGCCCTTTCA[-/C]CCATACACATTTGGC | 672 |
rs273900711 | snp | G/T | 3.30447e-05 | 0.00406464 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43091906 | AGAGGGGCCAAGAAA[G/T]TAGAGTCCTCAGAAG | 672 |
rs273900712 | snp | C/T | 9.89275e-05 | 0.00703235 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091882 | TCAGAAGAGAACTTA[C/T]CTAGTGAGGATGAAG | 672 |
rs273900713 | snp | A/C | 6.59315e-05 | 0.0057412 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43091869 | TATCTAGTGAGGATG[A/C]AGAGCTTCCCTGCTT | 672 |
rs273900714 | in-del | C/TCT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091814 | GTAAACAATATACCT[C/TCT]CAGTCTACTAGGCAT | 672 |
rs273900715 | snp | A/C | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104191 | AGATGAAGTTTCTAT[A/C]ATCCAAAGTATGGGC | 672 |
rs273900716 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091728 | TGAAGAATAGCTTAA[A/G]TGACTGCAGTAACCA | 672 |
rs273900717 | in-del | AGGC/CTCAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091688 | TATTGGCAAAGGCAT[AGGC/CTCAG]GAACATCACCTTAGT | 672 |
rs273900718 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091669 | CATCACCTTAGTGAG[-/G]AAACAAAATGTTCTG | 672 |
rs273900719 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091628 | TTCTTCACAGTGCAG[A/T]GAATTGGAAGACTTG | 672 |
rs273900720 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124099 | TCATTGGAACAGAAA[C/G]AAATGGATTTATCTG | 672 |
rs273900721 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091493 | TTTCAGATGATGAAG[-/AA]AGAGGAACGGGCTTG | 672 |
rs273900722 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43091093 | GAGAAGAAAAAGACA[A/C]AGCAAGTTGCAGCGT | 672 |
rs273900723 | in-del | -/GT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090931 | TCAGGTAAAAAGCGT[-/GT]GTGTGTGTGCACATG | 672 |
rs273900724 | in-del | A/TAAAAAGCGTGTGTGTGTGTG | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43090922 | TTTTAACCACTCAGG[A/TAAAAAGCGTGTGTGTGTGTG]CACATGCGTGTGTGT | 672 |
rs273900725 | in-del | -/TG | 0.0292914 | 0.117421 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43090921 | GCGTGTGTGTGTGTG[-/TG]CACATGCGTGTGTGT | 672 |
rs273900726 | snp | C/T | 6.86483e-05 | 0.00585828 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43090915 | GTGTGTGTGCACATG[C/T]GTGTGTGTGGTGTCC | 672 |
rs273900728 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082547 | TGCAACATAACCTGA[-/T]AAAGCTCCAGCAGGA | 672 |
rs273900729 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082529 | AGCTCCAGCAGGAAA[C/T]GGCTGAACTAGAAGC | 672 |
rs273900730 | in-del | CTA/TT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076579 | AAAGTAGTGAATACC[CTA/TT]TAAGCCAGAATCCAG | 672 |
rs273900731 | in-del | CTATAAGCCAGAA/TT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076569 | AAAGTAGTGAATACC[CTATAAGCCAGAA/TT]TCCAGAAGGCCTTTC | 672 |
rs273900732 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099984 | ACATGTTAGCTGACT[C/G]ATGATGGTCAATTTA | 672 |
rs273900733 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099883 | CTTTACCATACTGTT[-/T]AGCAGGAAACCAGTC | 672 |
rs273900734 | snp | C/G | 0.457037 | 0.140127 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074584 | GCTTTGGCTGCCCAG[C/G]AAGTATGATTTGTCC | 672 |
rs273900735 | snp | C/T | 0.000399281 | 0.0141238 | BRCA1 | 17 | allele_origin=T(germline)/C(unknown) | 17:43074611 | CTCTCTGACATGAGC[C/T]GTTTCATTTATGCTT | 672 |
rs273900736 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074490 | TGCCCATCATTAGAT[-/G]ATAGGTGGTACATGC | 672 |
rs273900737 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074363 | GGCCACACGATTTGA[C/T]GGAAACATCTTACTT | 672 |
rs273900738 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074300 | CTGTATTGGAACAAA[C/G]ACTTTGATTTTACTC | 672 |
rs273900739 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074324 | AAGATCTAGGTAATA[C/T]TTCATCTGCTGTATT | 672 |
rs273901740 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071202 | CTGGAATCAGCCTCT[C/T]CTCTGATGACCCTGA | 672 |
rs273901741 | snp | A/C | 1.65105e-05 | 0.00287315 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43071184 | CTGATGACCCTGAAT[A/C]TGATCCTTCTGAAGA | 672 |
rs273901742 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071022 | ATGCAATGGAAGAAA[A/G]TGTGAGCAGGGAGAA | 672 |
rs273901743 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099819 | GAACTCTGAGGACAA[A/C]GCAGCGGATACAACC | 672 |
rs273901744 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063870 | TTAGCTATTTCTGTA[-/T]AGTATAATACTATTT | 672 |
rs273901745 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063809 | CATTTTTACACCTAA[A/C]GTTTAACACCTAAGG | 672 |
rs273901746 | in-del | -/A | 0.000159987 | 0.00894248 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43063375 | TTCTATGATCTCTTT[-/A]GGGGTGACCCAGTCT | 672 |
rs273901747 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063415 | GTGAAAAGAGCACGT[A/T]CTTCTGCTGTATGTA | 672 |
rs273901748 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063439 | TGAATCGCTGACCTC[A/T]CTATCTCCGTGAAAA | 672 |
rs273901749 | snp | C/T | 0.000399281 | 0.0141238 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43063232 | CACTTTCCTTAACAA[C/T]GCACAAATTTTCCAT | 672 |
rs273901750 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063320 | GAGGTAAGTACTTGA[A/T]GTTACAAACTAACCA | 672 |
rs273901751 | in-del | -/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43063331 | AAATGCTGAATGAGG[-/T]AAGTACTTGATGTTA | 672 |
rs273901752 | in-del | -/AAGTACTTGATGT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063318 | AATGCTGAATGAGGT[-/AAGTACTTGATGT]TACAAACTAACCAGA | 672 |
rs273901753 | in-del | AGAGGAGATGTGGTCAATGGAAGAAACCACCAAGGTCCAA/TC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057081 | CATGATTTTGAAGTC[lengthTooLong]AGCGAGCAAGAGAAT | 672 |
rs273901754 | in-del | -/G | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43057051 | TCCCAGGACAGAAAG[-/G]TAAAGCTCCCTCCCT | 672 |
rs273901756 | in-del | -/GT/GTATTCCACTCC | 1.64727e-05 | 0.00286986 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43057003 | CACCCCACCACTCTG[-/GT/GTATTCCACTCC]TATTCCACTCCCCTT | 672 |
rs273901757 | in-del | -/GTATTCCACTCC/GTATTCCACTTC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056991 | CTGTATTCCACTCCC[-/GTATTCCACTCC/GTATTCCACTTC]CTTTGCAGAGATGGG | 672 |
rs273901758 | snp | A/C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056975 | TTTGCAGAGATGGGC[A/C/T]GCTTCATTTTGTAAG | 672 |
rs273901760 | in-del | -/CCA | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43051119 | TCTTCCTCTCTTCTT[-/CCA]GATCTTCAGGGGGCT | 672 |
rs273901761 | snp | A/C/G | 0.000132532 | 0.00813942 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43051085 | AATCTGTTGCTATGG[A/C/G]CCCTTCACCAACATG | 672 |
rs273901763 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050985 | ATAAGCAAGATCCCA[A/C/T]GATGGGGGTTCCTCA | 672 |
rs273901764 | in-del | -/TTA | | | splice-acceptor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43049196 | ATCTAAATGTCCATT[-/TTA]GATCAACTGGAATGG | 672 |
rs273901765 | in-del | -/T | | | splice-donor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43049119 | TCACCCTTGGCACAG[-/T]AAGTATTGGGTGCCC | 672 |
rs273901766 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049068 | ATATTCTCTCCTGTG[A/T]GCAAGACTGGCACCT | 672 |
rs273901767 | snp | A/G | 1.6486e-05 | 0.00287102 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43047713 | TGCTCTTTCCTTCCT[A/G]GGGATCCAGGGTGTC | 672 |
rs273901768 | snp | C/G/T | 3.29832e-05 | 0.00406085 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43047724 | GACACTTTGAATGCT[C/G/T]TTTCCTTCCTGGGGA | 672 |
rs273902769 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047645 | AGGACAATGGCTTCC[-/T]ATGGTAAGGTGCCTG | 672 |
rs273902770 | in-del | -/CT | 0.000164784 | 0.00907551 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43045811 | CTCTGCTTGTGTTCT[-/CT]GTCTCCAGCAATTGG | 672 |
rs273902771 | in-del | -/G | 0.000247245 | 0.0111158 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43099761 | GGGTAAGGGTCTCAG[-/G]TTTTTTAAGTATTTA | 672 |
rs273902772 | in-del | -/T | 0.5 | 0 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43097353 | TTTTCAACAAGTACA[-/T]TTTTTTAACCCTTTT | 672 |
rs273902773 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097357 | CTGTTTTTCAACAAG[-/T]ACATTTTTTTAACCC | 672 |
rs273902774 | in-del | -/A | 4.98782e-05 | 0.00499366 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43097298 | ATTTTTTGGGGGGAA[-/A]TTTTTTAGGATCTGA | 672 |
rs273902775 | in-del | A/GGTGACCCGAG | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045764 | GTGTGAGGCACCTGT[A/GGTGACCCGAG]AGTGGGTGTTGGACA | 672 |
rs273902776 | snp | A/C/G | 4.94385e-05 | 0.0049716 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43045766 | CACCTGTGGTGACCC[A/C/G]AGAGTGGGTGTTGGA | 672 |
rs273902777 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045636 | ACAGGACCCCAAGAA[A/T]GAGCTTACAAAGTGG | 672 |
rs273902778 | in-del | -/A | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124036 | AATGCTATGCAGAAA[-/A]TCTTAGAGTGTCCCA | 672 |
rs273902779 | snp | A/G | 1.749e-05 | 0.00295714 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43095861 | GATGAAATCAGTTTG[A/G]ATTCTGCAAAAAAGG | 672 |
rs273902780 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095801 | CACTGAAAAGAGAGT[A/G]GGTAGATACAGTACT | 672 |
rs273902781 | in-del | -/G | 0.00120476 | 0.0245139 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43094872 | TACCTTGTTATTTTT[-/G]TATATTTTCAGCTGC | 672 |
rs273902782 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095001 | AGTATGAGCTACATC[A/T]TCAGTATACTTGGTA | 672 |
rs273902784 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43094909 | AAGTATGTATTTTTT[-/T]AATGACAATTCAGTT | 672 |
rs273902785 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43094958 | AGTTTCTCTAATATA[C/G]CCAGTTGGTTGATTT | 672 |
rs273902786 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094777 | AACACCACTGAGAAG[C/T]GTGCAGCTGAGAGGC | 672 |
rs273902787 | in-del | -/CATCTG | | | cds-indel, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124018 | TTAGAGTGTCCCATC[-/CATCTG]TGGTAAGTCAGCACA | 672 |
rs273902788 | in-del | -/T | 9.58598e-05 | 0.00692248 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43115790 | CTTTTTCTCCCCCCC[-/T]ACCCTGCTAGTCTGG | 672 |
rs273902789 | in-del | -/C | 0.000585766 | 0.0171038 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43115790 | CTTTTTCTCCCCCCC[-/C]TACCCTGCTAGTCTG | 672 |
rs273902790 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115791 | TCTTTTTCTCCCCCC[-/C]TACCCTGCTAGTCTG | 672 |
rs273902791 | in-del | -/A | | | splice-acceptor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43115781 | CCCCCCTACCCTGCT[-/A]GTCTGGAGTTGATCA | 672 |
rs273902792 | snp | A/G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094683 | CTCATGCCAGCTCAT[A/G/T]ACAGCATGAGAACAG | 672 |
rs273903793 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094627 | ATGAATGTAGAAAAG[-/G]CTGAATTCTGTAATA | 672 |
rs273903794 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094567 | CAACATAACAGATGG[-/G]CTGGAAGTAAGGAAA | 672 |
rs367645566 | snp | A/G | 5.02795e-05 | 0.0050137 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067728 | ATTCCATTATCATGA[A/G]TTACCTCTAGCACAC | 672 |
rs367668867 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057462 | GTTGCAGTGAGCTGA[C/G]ATGGTGCCACTGCAC | 672 |
rs367719245 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064964 | GCCTCCTGAGTAGCT[A/G]GGACTACAGATGCCC | 672 |
rs367749335 | in-del | -/GGG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112734 | TCCTGACTATCACAA[-/GGG]GCTTGAAACCAAGCT | 672 |
rs367754170 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086620 | CTCTGGGAATAAGAT[C/T]AGAAATACAGAAAAA | 672 |
rs367807014 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051643 | TCTCCTCTGACTTTT[G/T]TTTTTTTTTTTGAGA | 672 |
rs367858125 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070241 | CCCGGCCATGCAATT[A/G]TTTTTATTATGAAGT | 672 |
rs367876926 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099726 | CAAAACTATAAGATA[A/G]GGAATCCAGCAATTA | 672 |
rs367911562 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068879 | AAAGAAATTTAGAGT[A/C]CTCTAGCTATTATCT | 672 |
rs367917055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110183 | ACAGGCGTGAGCCAC[C/T]GCACCCGGCCTCGAA | 672 |
rs367978134 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047732 | AAGGAAAGAGCATTC[A/C]AAGTGTCAAAGTAGG | 672 |
rs368058346 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057151 | CTGAAAGAAACCAAA[C/T]ACAACCCATCAGGAT | 672 |
rs368073959 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116679 | GTGCGCCACCACGCC[C/T]GGCTGATTTTTCGTA | 672 |
rs368080376 | in-del | -/AAAT | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047485 | TTTACAATATAAAAC[-/AAAT]AACAATAAAAACATC | 672 |
rs368119371 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116434 | GCAGTGGTGCAAACA[C/T]ACCTCACTGCAGCCT | 672 |
rs368128956 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111100 | ACAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 672 |
rs368134697 | snp | C/G | 6.0668e-05 | 0.0055073 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095820 | CTCTTTTCAGTGCCT[C/G]TTAAGTTGGCAAACT | 672 |
rs368142542 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064678 | TGCTCCCTCACAGAA[C/T]CCTTACAATTTTTGA | 672 |
rs368146955 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075348 | AACAAAAGCCAGCTA[C/T]AAAATATTGTTAGAA | 672 |
rs368150057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085549 | ACAAGTTGTTTTCCT[A/G]TAACACATGACAACT | 672 |
rs368252296 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104058 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAGAAA | 672 |
rs368350437 | snp | A/G | | | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43043897 | GACCACCCATTGCTG[A/G]TTTTGAAGATGGAGG | 672 |
rs368351285 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048019 | GCTCAACTTCACCCC[C/T]GGGATTATAGGCATG | 672 |
rs368415464 | snp | A/G | 0.000399281 | 0.0141238 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43104105 | AAGAAGAAGAAGAAG[A/G]AAACAAATGGTTTTA | 672 |
rs368447877 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086489 | ATCCCACTTCAATAG[A/T]TTTTCCTGCCTGTGC | 672 |
rs368480455 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057341 | ATGGTGAAACCTCAT[C/T]TCTACTAAAAATACA | 672 |
rs368590929 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101055 | TTTAAAAAGGATAAA[C/T]GATGACAATAAAACC | 672 |
rs368595091 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117495 | GCTTGTAATCCCAGC[A/T]CTTGGGAGGCCGAGG | 672 |
rs368621679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056685 | CTTGGGAAAAAAAAA[A/G]AGAGAGAGAGAGAGC | 672 |
rs368688955 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046500 | CATCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 672 |
rs368690455 | snp | C/T | 0.000148279 | 0.00860914 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091832 | AGGTATATTGTTTAC[C/T]TTACCAAATAACAAG | 672 |
rs368740506 | in-del | -/AG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056698 | GAAAAAAAAAAAGAG[-/AG]AGAGAGAGCAAGAGA | 672 |
rs368756704 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087429 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC | 672 |
rs368813459 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059635 | ACAAGATCTATTGTT[C/T]AAGCCAAAACCCAAG | 672 |
rs368888804 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076077 | TAGGTGACACAGGGC[G/T]ACCCTGTCTCAAAAA | 672 |
rs368950467 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106420 | TTTTTCCTACTGTGG[A/T]TGCTTCCAACCTAGC | 672 |
rs368951572 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122987 | GCATGAACCCGGGAG[C/G]CAGAGTTTGCAGTGA | 672 |
rs368952288 | in-del | -/CCT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095106 | ATGCAGAAACCACAC[-/CCT]CTATTTCTCTAACGT | 672 |
rs368967902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117575 | GAAACGCTGTCTCTA[C/T]TAAAAATACCAAAAC | 672 |
rs369034168 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119036 | CGGGATTACAGGCGT[G/T]AGCCACTACACTTAG | 672 |
rs369055904 | snp | A/G | 4.97616e-05 | 0.00498782 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091405 | TTCTATAAATAGACT[A/G]GGGCAAACACAAAAA | 672 |
rs369084576 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067887 | TGTCACCCAGGCTGG[A/G]GGTAAAAAAAAAAAA | 672 |
rs369124835 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112401 | TTGGACTTTTAATTC[C/T]AATATAACATTCAAA | 672 |
rs369133299 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059185 | ATTCATGCATCTGGC[C/T]GGGCACAGTGGCTCA | 672 |
rs369160739 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057451 | AGGAGGTGGAGGTTG[-/C]AGTGAGCTGAGATGG | 672 |
rs369181095 | snp | C/T | 1.65712e-05 | 0.00287843 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074305 | AAATCAAAGTGTTTG[C/T]TCCAATACAGCAGAT | 672 |
rs369198398 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066285 | ATCTGTCTCCTCCCT[A/T]TTTTGCTTTTTCATA | 672 |
rs369217270 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126897 | CAGCCAGCGCGAGTT[C/T]CAGGTGGGCGCGGGC | 672 |
rs369225701 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068307 | ATACCTGAAGTCTCA[A/G]ATAAATAGTTTAATA | 672 |
rs369230215 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113089 | ATTAGAGGCGTGAGC[C/G]ACCGTGCCCGGCCTC | 672 |
rs369294322 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108448 | GGGTGCAGTGGCTCA[C/T]GTCTGCAATCCCAGG | 672 |
rs369363742 | snp | A/G | 1.64955e-05 | 0.00287184 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094322 | TTTGGCATTTGATTC[A/G]GACTCCCCATCATGT | 672 |
rs369373293 | snp | A/G | 6.59435e-05 | 0.00574172 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093626 | TTGCAATTCAGTACA[A/G]TTAGGTGGGCTTAGA | 672 |
rs369375551 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064513 | GCAGTAGCTAAAGAA[-/A]TCACTTGTTTATTTC | 672 |
rs369394098 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094236 | TGAGGATCACTGGCC[A/G]GTAAGTCTATTTTCT | 672 |
rs369396089 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065594 | GCTTGAACCCGGGAG[G/T]GGGAGGTTGCAGCAA | 672 |
rs369461674 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106439 | TTCCAACCTAGCATC[A/G]TTACCAAATTATATA | 672 |
rs369477339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053400 | TGGCGTAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 672 |
rs369549959 | snp | C/T | 1.70006e-05 | 0.00291548 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071272 | GTTTAATTTACACAA[C/T]GATGAATGTTGAATT | 672 |
rs369588942 | snp | A/C | 8.23771e-05 | 0.0064173 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43094072 | TCTGTGGCTCAGTAA[A/C]AAATGCTCCTATAAT | 672 |
rs369627552 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047500 | AAATAACAATAAAAA[C/T]ATCAAAAAGACATTT | 672 |
rs369797788 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095398 | ACCAGCCTCGGTAAC[A/G]TGGTGAAACCCCATC | 672 |
rs369838168 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069293 | TCATCTTAATATGGG[-/G]CTTCAGAATTAATCA | 672 |
rs369844276 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110017 | CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAC | 672 |
rs369854869 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077433 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 672 |
rs369865630 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119849 | GGTAATTATAATCTA[A/C]ACTATATAAACACAC | 672 |
rs369893531 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066361 | ACTCTCAACAATACT[C/T]AAACTAGGTGTTACA | 672 |
rs369904906 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117451 | CTGTCTCAAAAAAAA[-/A]GAAAATAAGGCCAGA | 672 |
rs369913530 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113377 | ATTTTCTTTTCTTTT[C/T]TTTTTTTTCAGACAG | 672 |
rs369925993 | snp | A/C/T | 1.64825e-05 | 0.00287071 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43092261 | TTTATAGACCTCAGG[A/C/T]TGCAAAACCCCTAAT | 672 |
rs369978584 | snp | G/T | 1.66721e-05 | 0.00288717 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049234 | ATCACTGCAGTAATC[G/T]GCATACTTAACCCAG | 672 |
rs369982706 | snp | C/T | 1.65817e-05 | 0.00287933 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091951 | CCAAATGTGTATGGG[C/T]GAAAGGGCTAGGACT | 672 |
rs370012494 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114193 | CTGCCTTGGCCTCCC[A/G]AAGTGCTGGGGTTAT | 672 |
rs370039570 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081980 | CCTGAAGTATAGGAT[C/G]TCTCTCCCTATAAAT | 672 |
rs370041241 | in-del | -/CAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070583 | ACCCATGTGAGACAA[-/CAA]GGGGGAGAAAAAGAT | 672 |
rs370061993 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099980 | AAAATAAATTGACCA[C/T]CATCAGTCAGCTAAC | 672 |
rs370085206 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047396 | ATGAGCCACCATGCC[C/T]GGCCTTGATTTATGT | 672 |
rs370114428 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048400 | TAGAGACGGGGTTTC[A/G]CCATGTTGGTTGGCC | 672 |
rs370142241 | in-del | -/GTTGG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074727 | ATAACATGGGGTTGG[-/GTTGG]TCTGAGGCACCATAT | 672 |
rs370148636 | in-del | -/A | 0.411746 | 0.190626 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046757 | GTGAGACTCCACCTC[-/A]AAAAAAAAAAAAAAA | 672 |
rs370199866 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43053940 | CGCCATTGTACTTCA[A/G]CCTGGGCAAGAAGAG | 672 |
rs370254862 | snp | A/C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106191 | AGACAATGGGGGCAC[A/C/G]GCGATACAGCCCTAC | 672 |
rs370299792 | snp | A/G | 3.31038e-05 | 0.00406827 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43067594 | AAGGTATTCTGTAAA[A/G]GTTCTTGGTATACCT | 672 |
rs370366788 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096495 | GAGAATCGCTTGAAC[-/C]AGGGAGTTGGAGATT | 672 |
rs370473459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072857 | GCGTAAGCCACCCAC[C/T]ACGCCTGGCCCCAGC | 672 |
rs370474677 | in-del | -/AAC | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124173 | GGTTTATAAAATGAC[-/AAC]TTCATTTTATCATTT | 672 |
rs370536578 | snp | C/T | 3.34689e-05 | 0.00409064 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063404 | AAAAGACAGGTTACA[C/T]ACAGCAGAAGAACGT | 672 |
rs370570158 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051798 | CGCACCACCACGCCC[A/G]GCTAATTTTTGTATT | 672 |
rs370673239 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085778 | TGCAGCAGAGCAGCC[A/G]GAACTGGTCTGGAGG | 672 |
rs370677799 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116680 | TGCGCCACCACGCCC[A/G]GCTGATTTTTCGTAT | 672 |
rs370751110 | in-del | -/TTCATCAGTAGGGGTTTCAAGCTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112721 | CTGACTATCACAATC[-/TTCATCAGTAGGGGTTTCAAGCTT]CTGACTATCACAAGC | 672 |
rs370818885 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056531 | GGCACGGTGGCTCAC[A/G]CCTATCCCAGCACTT | 672 |
rs370832723 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066671 | GCCTCAGGCTCCCAA[A/C]GTGCTGGGATTACTG | 672 |
rs370884761 | snp | C/G | 0.000200538 | 0.0100114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082623 | AAATACTTTGAGAAG[C/G]TTTCCATTAAATGAA | 672 |
rs370890414 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121172 | CAAGGTCAGGAGATC[A/G]AGACCATCTTGGCTA | 672 |
rs370914983 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085289 | TCACTTGAACCCAGG[G/T]GGCGGAAGTGCAGTG | 672 |
rs370958086 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097766 | CAATCTCAGAGGTCT[A/G]ACAAGCATCTAATGA | 672 |
rs370965853 | snp | C/T | 0.000120106 | 0.00774845 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124139 | CATTAGAAAAACATA[C/T]ATATATATCTTTTTA | 672 |
rs370969077 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115536 | ATATATGTCAAAACT[G/T]TACCAGGAACTATGA | 672 |
rs370999077 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082515 | GCTGTTCTAACACAG[C/T]TTCTAGTTCAGCCAT | 672 |
rs371005195 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107110 | CGCTCTGTCTCCCAG[C/G]CTGGAGTGCAGTGGC | 672 |
rs371035497 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106136 | AAAAAAAAAAAAAAA[-/G]AAAAGGAAACACAAT | 672 |
rs371058439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079008 | AGTTTGAGACCAGCC[C/T]GGCCAACATGGTGAA | 672 |
rs371068489 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115971 | CAGAGAATACGATCC[C/T]TACCTTCAGTGAGCT | 672 |
rs371133200 | snp | A/T | 0.49823 | 0.0296997 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112733 | AATCCTGACTATCAC[A/T]AGCTTGAAACCAAGC | 672 |
rs371203180 | snp | C/G | 8.23608e-05 | 0.00641667 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057020 | AGAGTGGTGGGGTGA[C/G]ATTTTTGTCAACTTG | 672 |
rs371296340 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117194 | TGCCTGTAATCCTAG[C/T]ACTTTGGGAGGCTGA | 672 |
rs371380546 | snp | C/T | 0.000197873 | 0.00994471 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076449 | CAATATAAATAAAGA[C/T]GTCAGATACCACAGC | 672 |
rs371465813 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055023 | CCAAAGTGCTGGGAT[C/G]ACAGGTGTGAGCCAC | 672 |
rs371502197 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064417 | CCCTAGAATGTCTAC[C/T]TGGGGAGTCCTAACC | 672 |
rs371510602 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076268 | TGACCTTCAGAAGGG[A/C]CATATCTATCTAACC | 672 |
rs371540942 | snp | A/G | 0.000723327 | 0.0190037 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045414 | TGCTCAATTGGTGGC[A/G]TTTAAATGGTTTTAA | 672 |
rs371567044 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103445 | GCGCTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 672 |
rs371631805 | snp | C/T | 3.30409e-05 | 0.0040644 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093729 | GGTGCTTTTGAATTG[C/T]GGATATTTAATTCGA | 672 |
rs371658650 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114252 | AGTCCCTGTAATAAT[-/A]GTATAGTATGTTCAG | 672 |
rs371690590 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087040 | ATTTTAAAACTGGAT[A/G]TCACCCAGTGTTGGC | 672 |
rs371696038 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064310 | AATGTGGACGGAGAA[C/T]ATCTATATTACTAGA | 672 |
rs371730202 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075494 | TATTGGGTGCTTACT[A/G]TGGGTCAAATACTAA | 672 |
rs371762586 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059034 | GACATTTCCTAGTTA[C/G]TTGAATGAGGAGTCT | 672 |
rs371770883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079714 | ACCCAGAGAAGCACA[C/T]TTTGTGAGAACCAAT | 672 |
rs371822984 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068233 | AGTAAGCCGAGATGG[C/T]GCCACTGCACTCTAG | 672 |
rs371829475 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110992 | TGTAATCCCAGCTAC[G/T]TGGGAGGCTGAGGCA | 672 |
rs371909810 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125597 | AAGAGGAAGAATTCT[A/C]CCTGAGTTTGCCATA | 672 |
rs371932696 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069558 | TAAGGAATTCTGGAC[A/G]TGCAGGCAAGTGATC | 672 |
rs371973519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104104 | GAAGAAGAAGAAGAA[A/G]AAAACAAATGGTTTT | 672 |
rs372002119 | snp | C/T | 8.26685e-05 | 0.00642864 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093914 | TTGACCATTCTGCTC[C/T]GTTTGGTTAGTTCCC | 672 |
rs372017932 | snp | C/T | 4.94474e-05 | 0.00497205 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093179 | GCTAACTTCCAGTAA[C/T]GAGATACTTTCCTGA | 672 |
rs372047427 | snp | C/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124030 | ACCAGATGGGACACT[C/G]TAAGATTTTCTGCAT | 672 |
rs372105637 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069061 | ATTTACGTGTTGCAC[A/C]ATACTGCCATGAAGG | 672 |
rs372133569 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051779 | GTAGCTGGGATTACA[C/G]GCGCGCACCACCACG | 672 |
rs372298578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080356 | ATGTGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 672 |
rs372366481 | snp | A/T | 1.64754e-05 | 0.00287009 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093225 | CCAGGTACCAATGAA[A/T]TACTGCTACTCTCTA | 672 |
rs372391060 | snp | A/C | 0.000116074 | 0.00761731 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051050 | GAACTCTGGGGTTCT[A/C]CCAGGCTCTTACCTG | 672 |
rs372396487 | snp | G/T | 9.88452e-05 | 0.00702942 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091709 | TGCCTTTGCCAATAT[G/T]ACCTGGTTACTGCAG | 672 |
rs372400428 | snp | A/G | 0.000115482 | 0.00759787 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094289 | TACCTCATTTAGAAC[A/G]TCCAATACATCAGCT | 672 |
rs372486277 | in-del | -/CA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099411 | GAGTAGCTGGGATTA[-/CA]GTTATGTGCCACCAC | 672 |
rs372536342 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119361 | CAACTCTTGTAATCA[A/T]GGGGTTTTTGACATA | 672 |
rs372544924 | snp | C/T | 0.40733 | 0.194287 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056191 | TTTTTTTTTTTTTTT[C/T]TTTTGAGATCTTCTG | 672 |
rs372606073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117794 | CATCACCCAAGTTCC[C/T]ATCCCTACCTGTCTA | 672 |
rs372629702 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117899 | TACTATATTCAAGTA[C/G]TATTCTAGGAGATAG | 672 |
rs372652783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113610 | CTGACCTCGTGATCC[A/G]CCCACCTCGACCTCC | 672 |
rs372736366 | in-del | -/TCC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123323 | TCTTCCAAATACCTA[-/TCC]TCTCAACGACACCGA | 672 |
rs372740159 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048045 | GCATGAGCCACCGCA[C/G]CCAGCCTTGGCTAAT | 672 |
rs372783383 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087161 | GTATCAAACACCAAA[A/C]TCCTAGTCCCAGTAA | 672 |
rs372842137 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052772 | CCCTTGACAGACAGA[C/T]GGACAGAAACACACA | 672 |
rs372920589 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102413 | CCAGGCTGGAGTGCA[A/G]TGGCGCAATCTCGGC | 672 |
rs372922938 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43078034 | GCCACTGCGCCCGAC[C/T]GTTATTTTTCAACGA | 672 |
rs372942700 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124722 | TTCCACAAGGTCCCA[C/T]CCTCTCATACATACC | 672 |
rs373033433 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088387 | TTTTTTTTTTTAACT[A/G]CTCCTTGTGGAGCAA | 672 |
rs373063527 | in-del | -/CTCT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123325 | TTCCAAATACCTATC[-/CTCT]CAACGACACCGATCA | 672 |
rs373070538 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054008 | AAGTTTCACCTCTAC[A/G]TATACATTTCTCTTC | 672 |
rs373097715 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096104 | AATGGTTGCTGGGCA[C/T]GGTGGCTCAAGCCTG | 672 |
rs373185847 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119404 | GAAAAGAAAAACAAT[-/G]AACTAAGTCAGGAGG | 672 |
rs373202012 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104070 | CTCAAAAAAAAAAAA[-/G]AAAAAAAAAAGAAAA | 672 |
rs373207084 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092953 | TTGAAACCTTGAATG[C/T]ATTCTGCAAATACTG | 672 |
rs373218165 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094414 | TGCTATTTAGTGTTA[C/T]CCAAGGAACATCTTC | 672 |
rs373323531 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045115 | AGGTTTCAAGTTTCC[G/T]TTTCATTTCTAATAC | 672 |
rs373353131 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058707 | CCTAAATCAATTGTA[-/T]ATTATCATCTAAGGA | 672 |
rs373363231 | snp | A/T | 4.14036e-05 | 0.00454973 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106560 | AAAGAAAGAAAGAAC[A/T]ATTTAATTTACTTCC | 672 |
rs373404078 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060212 | CCGTGTAGCTGGGAT[C/T]AGAGGCACGCGCCAC | 672 |
rs373413230 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106018 | TGTAGTCCCAGCTAT[C/G/T]TGGGAGGCTAAGGCA | 672 |
rs373413425 | in-del | -/AAAAAAAAGAAAAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104073 | AAAAAAAAAAAAGAA[-/AAAAAAAAGAAAAG]AAGAAGAAGAAGAAG | 672 |
rs373483619 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127036 | CGCTTGAATTCTCAC[C/T]GGGCCCCAGCCGCCC | 672 |
rs373488596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084309 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 672 |
rs373495074 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082081 | ATAGCTTTCTGAAAT[C/T]ATGGGGTTGCCTGTC | 672 |
rs373539054 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118229 | AGCAGGACCATGCCT[A/G]TGTATGCAGGACATC | 672 |
rs373592036 | snp | C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080979 | TTTAGGGAGAAAAAG[C/G/T]CTCAAAACTTATGTT | 672 |
rs373655067 | snp | C/T | 1.68015e-05 | 0.00289836 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43106489 | TTACATAAAGGACAC[C/T]GTGAAGGCCCTTTCT | 672 |
rs373676607 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067501 | TCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 672 |
rs373681653 | snp | C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116119 | CACTATCACTGTGGG[C/G/T]GCACATCTCATCTTT | 672 |
rs373686790 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074371 | TGTTTCCGTCAAATC[A/G]TGTGGCCCAGACTCT | 672 |
rs373693434 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064111 | AGGCTGAAAACACCA[C/T]TAATTATAACCAGCA | 672 |
rs373703115 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068624 | ATATCATTCGATTCC[C/T]TAAGATCGTTTCTTT | 672 |
rs373748868 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120183 | CTGAAAGTCAAAAAT[A/G]TTATAGTCATAGGTA | 672 |
rs373792619 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120706 | GGAGGCGGAGCTTGC[A/G]GTGAGCCGAGATGGC | 672 |
rs373810778 | snp | C/T | 1.65081e-05 | 0.00287293 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43049139 | GCCAAGGGTGAATGA[C/T]GAAAGCTCCTTCACC | 672 |
rs373851033 | in-del | -/GAAAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074935 | AGAAAGAAAGGAAAG[-/GAAAG]AAAGGAAAGAAAAGG | 672 |
rs373958534 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114759 | GTACCAGGTTATGTA[C/G]CAGGTACATAAATAC | 672 |
rs374082362 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097125 | ATAACAAACTGCACA[G/T]ACATCCCTGAACCTA | 672 |
rs374087794 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127140 | GGCCTGAGCCTCCCC[A/G]ACGGGCACCGCCCCC | 672 |
rs374109544 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071672 | AATATATTAAAGACA[C/T]CTAAGCAATATTATT | 672 |
rs374192364 | snp | C/T | 1.64887e-05 | 0.00287125 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091448 | ACCTAAGTTTGAATC[C/T]ATGCTTTGCTCTTCT | 672 |
rs374211862 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074728 | TAACATGGGGTTGGG[C/T]TGGTCTGAGGCACCA | 672 |
rs374257806 | snp | C/T | 1.65776e-05 | 0.00287898 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105000 | TCAGCAAGTGATTAT[C/T]AACCTTTTAAGGACA | 672 |
rs374363209 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047484 | TTTTACAATATAAAA[C/T]AAATAACAATAAAAA | 672 |
rs374416358 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082561 | TATCAGGTTATGTTG[C/G]ATGGTATCCCTCTGC | 672 |
rs374435098 | snp | C/T | 1.81641e-05 | 0.00301359 | intron-variant, splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43079400 | CATGTATATGCGAAT[C/T]TGTAAGAAAGGTGAA | 672 |
rs374519494 | snp | A/G | 0.000146767 | 0.00856517 | intron-variant, missense | BRCA1 | GRCh38.p7 | 17:43079339 | GGAGAGGCACCTGAT[A/G]TATGTTCTCTAGGCC | 672 |
rs374524253 | in-del | -/G | | | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125558 | CCCAGTCTGCCCCCG[-/G]ATGACGTAAAAGGAA | 672 |
rs374547377 | snp | C/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126773 | GCCCGCCACTGCGCT[C/G]TGGGGGCCCCTCTCT | 672 |
rs374565580 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073480 | CATGGCCAAATACCA[C/G]ATTTGATGCCAAACA | 672 |
rs374568940 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100529 | GTGTGTGTGTGTATA[C/T]ATATATACATATATA | 672 |
rs374570872 | in-del | -/CGCGTG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090746 | CTGTGTGTGCGCGTG[-/CGCGTG]TGCGTGTGTGTGAAA | 672 |
rs374579692 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095409 | TAACATGGTGAAACC[C/T]CATCTCTATAAAACC | 672 |
rs374604399 | snp | A/G | | | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044127 | TCTGACCTTGCAACA[A/G]TTTGTTTTGGCAGCA | 672 |
rs374751811 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067834 | GAACTATTTAAAGTG[-/A]AATTTTTTTTTTTTT | 672 |
rs374788793 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087757 | TTCTTGTTTTTGAGA[C/T]AGGGTCTCACCATAT | 672 |
rs374789098 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059111 | ACCCCTGAGCTTCAT[A/G]CAATGTGTCCAACTG | 672 |
rs374842106 | in-del | -/T | 0.499946 | 0.00519141 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112727 | TATCACAATCCTGAC[-/T]ATCACAAGCTTGAAA | 672 |
rs374857614 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107852 | ATAATTAAAAGCAGC[A/G]ATTCACTCATACAAC | 672 |
rs374857952 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108811 | CAGCCTGACCAACAC[A/G]GAGAAACCCTGTCTC | 672 |
rs374865089 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060977 | CTAAAAATAAAAACT[A/C]GTCGGGTGTGGTAGC | 672 |
rs374865488 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046846 | TGACAGTGAAAGCCC[A/C]CAGCCTCTGGCAACT | 672 |
rs374899930 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110047 | CTACAGGTGCCCGCT[A/T]CCACGCCTGGCTAAC | 672 |
rs374914131 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069604 | AGACACAGGTAAGAG[C/T]TTTCAGAGCAAATTG | 672 |
rs375003483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124592 | TGTTACTACTGACGC[G/T]CCTCTACTTCCCTCT | 672 |
rs375042815 | snp | A/G | 1.66621e-05 | 0.00288631 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43045658 | GGGTCCTGTGGCTCT[A/G]TACCTGTGGCTGGCT | 672 |
rs375055113 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116838 | GTGTCTTCTGATCTA[C/T]AGGTGTCTCTTACTT | 672 |
rs375078966 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43045923 | TGAGGTAGAAGCTAA[-/T]TTTTTTTTTTTTTTT | 672 |
rs375098248 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085486 | CATAGCATTCAAAAG[C/G]CCCTTTATACCCTGG | 672 |
rs375117640 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051794 | GGCGCGCACCACCAC[A/G]CCCGGCTAATTTTTG | 672 |
rs375172267 | in-del | -/AAAC | 0.00307881 | 0.0391143 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095588 | CCCCATCTCAAAAAA[-/AAAC]AAACAAACAAACAAA | 672 |
rs375177224 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102698 | TGCTTTGCCGCCCAC[A/G]CTGAAGTGCAGTGGA | 672 |
rs375256729 | in-del | -/CTTTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113377 | ATTTTCTTTTCTTTT[-/CTTTT]TTTTCAGACAGAGTC | 672 |
rs375310065 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090750 | TGTGTGCGCGTGTGC[A/G]TGTGTGTGAAATAAA | 672 |
rs375310294 | snp | C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057912 | GTAGTCCCAGCTACT[C/G/T]GGGAAGCTGAGGCAT | 672 |
rs375357592 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044630 | TATATTTTAAGAGGA[A/G]TGGATTATATACCAG | 672 |
rs375483589 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113124 | GCTGTCTTTACCTCC[A/C]ACTTCACTGGGCTCA | 672 |
rs375508764 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057028 | GGGGTGAGATTTTTG[C/T]CAACTTGAGGGAGGG | 672 |
rs375633490 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117318 | GTGGTGGCGCATGCC[C/T]GTGGTCTCAGCTACT | 672 |
rs375639469 | snp | A/G | 1.66751e-05 | 0.00288744 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43063376 | GACTGGGTCACCCCT[A/G]AAGAGATCATAGAAA | 672 |
rs375647048 | snp | C/T | 0.000101143 | 0.00711064 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063295 | AACTATATGACTGAA[C/T]GAATATCTCTGGTTA | 672 |
rs375652632 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111670 | ACTAAAAATACAAAA[A/C]AATTAGCTGGGCGTG | 672 |
rs375673256 | snp | C/T | 0.499984 | 0.00279548 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112736 | CCTGACTATCACAAG[C/T]TTGAAACCAAGCTTC | 672 |
rs375679298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057432 | AGGAGAATCTTTTGA[A/C]TGCAGGAGGTGGAGG | 672 |
rs375719814 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083113 | CCTGCCTAGATTACT[A/G]GCTTGTGAGGACTCT | 672 |
rs375723816 | in-del | -/TA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073749 | TAAAATATATGTGTG[-/TA]TATATATATATATAT | 672 |
rs375819480 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046193 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 672 |
rs375835931 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096356 | TACTCCAGCCTGGGC[A/T]ACAGAGCAAGACTCT | 672 |
rs375865273 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056358 | TTGTATATTTTTTTT[-/T]GGTAGAGATGGGGTT | 672 |
rs375952040 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095853 | GCCATTACCCTTTTT[C/T]GCAGAATCCAAACTG | 672 |
rs375953953 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087363 | AAAATGAAGTCACTT[A/G]AGAATTTTAACGACC | 672 |
rs376001155 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116582 | GGCATGCAATGGTGC[A/G]ATCTCGGCTCACTGC | 672 |
rs376068488 | in-del | -/TTCATCAGTAGGGGTTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112743 | TCACAAGCTTGAAAC[-/TTCATCAGTAGGGGTTT]CAAGCTTCTCACTCT | 672 |
rs376145469 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110173 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 672 |
rs376168245 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050556 | AGGTGGAGGTTGCAG[G/T]GAGCCGAGATCGCGC | 672 |
rs376173321 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073191 | CAAATTATCTTTTTT[A/G]TTCCCTATATTGTCC | 672 |
rs376210174 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103004 | TTGCCCAAGCTGGGC[C/T]CAAAGGACCTCCTAC | 672 |
rs376221406 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077261 | CTTAAATAATACATG[C/G]AACTAATGATGAAAT | 672 |
rs376248126 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046085 | TGCCATCACACCCAG[A/C]TAATTTTTGTATTTT | 672 |
rs376274188 | snp | C/T | | | upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125543 | GCTCTGGATTGGCCA[C/T]CCAGTCTGCCCCCGG | 672 |
rs376309842 | in-del | -/AAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050616 | TCGACCTCAAAAAAA[-/AAG]AAAAAAAAAAAGAAA | 672 |
rs376335621 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103335 | AGCCAGGTCTGGTGT[C/T]GTACCCCTGTAGTCC | 672 |
rs376387696 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089050 | AGGCCTGGTGGCTCA[C/T]GCCTGTAATCTCAGC | 672 |
rs376396892 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066769 | GTCCCAGCAGGTAGA[C/T]AGGAGTTAATAGTTG | 672 |
rs376407330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070747 | AGATAAAGCTATAGT[A/G]TGGATTATTTTATGT | 672 |
rs376470635 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065754 | TAGAAAGATTTTAGA[A/G]TTGAGCCACACAATC | 672 |
rs376501348 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070818 | CACAGAACTGTGATT[-/G]TTTTCTAGATTTCTT | 672 |
rs376586685 | snp | A/C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048025 | CTTCACCCCCGGGAT[A/C/T]ATAGGCATGAGCCAC | 672 |
rs376618168 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113866 | GGTAGCTGAAGTCAG[G/T]AGTTTGAGAGCAGCC | 672 |
rs376647498 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047779 | TTCATCATTTTTTTT[-/T]GTTTGTTTTTGAGAC | 672 |
rs376657193 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080581 | AGGCTGAGGTGAGAG[A/G]ACTGCTTGAGTCCAG | 672 |
rs376686434 | in-del | -/ACAC/ACACAC/ACACACAC | 0.212425 | 0.24716 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086109 | TTTTATCACATACAT[-/ACAC/ACACAC/ACACACAC]ACACACACACACACA | 672 |
rs376721828 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115256 | CGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 672 |
rs376736915 | snp | C/G | 1.66579e-05 | 0.00288595 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063366 | TTCTTTAATAGACTG[C/G]GTCACCCCTAAAGAG | 672 |
rs376836050 | snp | A/T | 0.000170739 | 0.00923798 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43063854 | TAAAGGGAGGAGGGG[A/T]GAAATAGTATTATAC | 672 |
rs376868298 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089783 | GGGAGGCTGAGGTGG[G/T]ATCACTTGAGCCCAG | 672 |
rs376944417 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123074 | AAAAAGAAAAAAAAA[A/C/T]ACAAAAATTAGCTGG | 672 |
rs376994550 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106390 | AGGAACGCTATGTTA[C/T]TAAATAATTTCTACT | 672 |
rs377034087 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099581 | TGGCCTCTTTTGCTC[C/T]CTTTTTAAAGTAAGA | 672 |
rs377043961 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069306 | GGGCTTCAGAATTAA[C/T]CATGTGTAATACAGT | 672 |
rs377064695 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084011 | CTGGGATTACAGGCA[-/C]CTGTTACCATGCCCG | 672 |
rs377107671 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065946 | AGTATTTCAAGTTAC[C/T]TTTATGTATCTTTAC | 672 |
rs377114453 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095119 | CACCTATTTCTCTAA[C/T]GTCTAAGAGTGAATT | 672 |
rs377293041 | in-del | -/CTCT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049096 | TATTGTGTCCTCCCT[-/CTCT]GACAGGGCACCCAAT | 672 |
rs377310179 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094459 | TCTCTGAGCATGGCA[A/G]TTTCTGCTTATTCCA | 672 |
rs377388626 | snp | C/G | 0.000155988 | 0.00883005 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106575 | AATTTAATTTACTTC[C/G]TTTTGTAGAAAGAAT | 672 |
rs377394795 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054907 | GGTGCCTACCACCAC[A/G]CCCAGTTAACTTTTG | 672 |
rs377396138 | in-del | -/TACAGT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109071 | ACCTATCTATCTGTC[-/TACAGT]CTTGAACTCCCGACC | 672 |
rs377444317 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084940 | AAATCAGAAAAAGTA[A/G]TGGGGTAATTATTAA | 672 |
rs377466939 | in-del | -/TAAT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100677 | ATATATATATATATA[-/TAAT]ATATATATATATATA | 672 |
rs377475866 | snp | A/C/G/T | 3.2961e-05 | 0.00405951 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/A(germline)/C(germline) | 17:43093013 | TGCTTGTTTCCCGAC[A/C/G/T]GTGGTTAACTTCATG | 672 |
rs377541153 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066359 | AAACTCTCAACAATA[C/T]TCAAACTAGGTGTTA | 672 |
rs377570241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119551 | GAATAAAATTAAATG[C/T]TACTTGGGAAAATGC | 672 |
rs377595653 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057123 | CCACATCTCCTCTGA[C/G]TTCAAAATCATGCTG | 672 |
rs377605733 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127180 | GCGCCCGGTCCCATC[A/G]ACTGCCCAAGGGCTG | 672 |
rs377611452 | snp | C/G | 0.49823 | 0.0296997 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112732 | CAATCCTGACTATCA[C/G]AAGCTTGAAACCAAG | 672 |
rs377617416 | in-del | -/TTTTG | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124773 | TTTTGTTTTGTTTTG[-/TTTTG]AGACAGTCTCGCTCT | 672 |
rs377629427 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074390 | GGCCCAGACTCTTCC[A/G]GCTGTTGCTCCTCCA | 672 |
rs377647919 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089697 | TTTTTTAAAGAAAAA[A/G]GATGATTTATGAGCA | 672 |
rs377699724 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126862 | CGGGTGTGGGAACTG[G/T]GGCTGCGCGCAGCGC | 672 |
rs377703638 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047234 | CTTCCCAAGTAGCTG[C/T]GACTACAGGCATCTG | 672 |
rs386134270 | in-del | C/GTA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092695 | ATAATGCCAAATGTA[C/GTA]TCAAAGGAGGCTCTA | 672 |
rs386364978 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116199 | CTAGAACTTTTTTTT[-/T]GTTTACTGTAAATGC | 672 |
rs386797189 | multinucleotide-polymorphism | AA/TG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051308 | TGTCCAGAACACTAC[AA/TG]GATTTCAGAAGATCT | 672 |
rs386797190 | multinucleotide-polymorphism | AG/CC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077559 | GGCTAGTCTCGAACT[AG/CC]TGACCTCAAGTGATC | 672 |
rs386797191 | multinucleotide-polymorphism | ATA/TTG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085995 | AGTTTTGTCGACATG[ATA/TTG]TGAATATTTTCAAAT | 672 |
rs386797193 | in-del | AAC/CACT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116189 | TGAATTCCTTCCTAG[AAC/CACT]TTTTTTTTGTTTACT | 672 |
rs386833394 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091569 | TCTTGATTGGTTCTT[A/C/G]CAAACAAATGAGGCA | 672 |
rs386833395 | in-del | -/AG | 0.000479335 | 0.0154738 | BRCA1, NBR2 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43124028 | TGCAGAAAATCTTAG[-/AG]TGTCCCATCTGGTAA | 672 |
rs387906563 | in-del | -/AGCCATGTGG/GAGCCATGTGG/NNNNNNNNNN | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094706 | TGTGGAGCCATGTGG[lengthTooLong]CACAAATACTCATGC | 672 |
rs387906564 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091906 | AGAGGGGCCAAGAAA[-/T]TAGAGTCCTCAGAAG | 672 |
rs397507180 | in-del | -/TGTTAGGTTCTGATGACTCACATGATGGGGAGTCTGAATCA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094316 | CCAGAAGTGATGAAC[lengthTooLong]AATGCCAAAGTAGCT | 672 |
rs397507181 | in-del | -/TGTTAGGTTCTGATGACTCACATGATGGGGAGTCTGAATCAA | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094315 | CCAGAAGTGATGAAC[lengthTooLong]ATGCCAAAGTAGCTG | 672 |
rs397507182 | in-del | -/TGTTAGGTTCTGATGACTCACATGATGGGGAGTCTGAATCAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094314 | CCAGAAGTGATGAAC[lengthTooLong]TGCCAAAGTAGCTGA | 672 |
rs397507183 | in-del | -/TGTTAGGTTCTGATGACTCACATGATGGGGAGTCTGAATCAAAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094313 | CCAGAAGTGATGAAC[lengthTooLong]GCCAAAGTAGCTGAT | 672 |
rs397507184 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094329 | ATGACTCACATGATG[A/C/G]GGAGTCTGAATCAAA | 672 |
rs397507185 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106548 | AATTGTTCTTTCTTT[C/G]TTTATAATTTATAGA | 672 |
rs397507186 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106540 | TTTCTTTCTTTATAA[-/A]TTTATAGATTTTGCA | 672 |
rs397507187 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094126 | ACCTATCGGAAGAAG[A/G]CAAGCCTCCCCAACT | 672 |
rs397507188 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093999 | GGAGACCTACATCAG[G/T]CCTTCATCCTGAGGA | 672 |
rs397507189 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106507 | TGAAACTTCTCAACC[A/G]GAAGAAAGGGCCTTC | 672 |
rs397507190 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093859 | CATGAGAATAAAACA[A/C]AAGGTGATTCTATTC | 672 |
rs397507191 | snp | A/C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093841 | GGTGATTCTATTCAG[A/C/T]ATGAGAAAAATCCTA | 672 |
rs397507192 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093802 | GAATCACTCGAAAAA[-/A]GAATCTGCTTTCAAA | 672 |
rs397507193 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093677 | GAAGTCTTCTACCAG[-/G]CATATTCATGCGCTT | 672 |
rs397507194 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093609 | GTACTGAATTGCAAA[-/A]TTGATAGTTGTTCTA | 672 |
rs397507195 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093559 | AAAAAGTACAACCAA[-/A]TGCCAGTCAGGCACA | 672 |
rs397507196 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093324 | AAGAAGAGAAACTAG[A/C]AACAGTTAAAGTGTC | 672 |
rs397507197 | in-del | -/T/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093316 | AAACTAGAAACAGTT[-/T/TT]AAAGTGTCTAATAAT | 672 |
rs397507198 | snp | A/C/G | 3.29527e-05 | 0.00405898 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43093250 | AGGGTTTTGCAAACT[A/C/G]AAAGATCTGTAGAGA | 672 |
rs397507199 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093202 | GTACCTGGTACTGAT[G/T]ATGGCACTCAGGAAA | 672 |
rs397507200 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093107 | TCAGTGTGCAGCATT[-/T]GAAAACCCCAAGGGA | 672 |
rs397507201 | snp | A/G | 0.000131848 | 0.00811828 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093105 | AGTGTGCAGCATTTG[A/G]AAACCCCAAGGGACT | 672 |
rs397507202 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092829 | GTCCAAAAGTCACTT[C/T]TGAATGTGAACAAAA | 672 |
rs397507203 | snp | A/G | 1.648e-05 | 0.0028705 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092817 | CTTTTGAATGTGAAC[A/G]AAAGGAAGAAAATCA | 672 |
rs397507204 | snp | A/G | 6.59152e-05 | 0.00574049 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092796 | AAGAAAATCAAGGAA[A/G]GAATGAGTCTAATAT | 672 |
rs397507205 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092666 | TAGGTTTTGTCTATC[-/T]ATCTCAGTTCAGAGG | 672 |
rs397507206 | snp | A/C/T | 3.30786e-05 | 0.00406672 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43092568 | TTTTTCCCATCAAGT[A/C/T]ATTTGTTAAAACTAA | 672 |
rs397507207 | in-del | -/GT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092549 | TTGTTAAAACTAAAT[-/GT]AAGAAAAATCTGCTA | 672 |
rs397507208 | in-del | -/GA | 1.64939e-05 | 0.0028717 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43092493 | ATGTCACCTGAAAGA[-/GA]AATGGGAAATGAGAA | 672 |
rs397507209 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092422 | AGAGAAAATGTTTTT[-/T]AAAGAAGCCAGCTCA | 672 |
rs397507210 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092357 | AGTGGGCTCCAGTAT[-/T]AATGAAATAGGTTCC | 672 |
rs397507211 | snp | G/T | 1.648e-05 | 0.0028705 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43092346 | GTATTAATGAAATAG[G/T]TTCCAGTGATGAAAA | 672 |
rs397507212 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092322 | ATGAAAACATTCAAG[C/G]AGAACTAGGTAGAAA | 672 |
rs397507213 | snp | A/C/G | 3.29636e-05 | 0.00405964 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43092284 | CCAAAATTGAATGCT[A/C/G]TGCTTAGATTAGGGG | 672 |
rs397507214 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104234 | ATAATTTTGCAAAAA[-/A]GGAAAATAACTCTCC | 672 |
rs397507215 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092179 | TATGAAGAAGTAGTT[C/T]AGACTGTTAATACAG | 672 |
rs397507216 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092028 | CTAGTTTTGCTGAAA[-/A]TGACATTAAGGAAAG | 672 |
rs397507217 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091848 | TTCCCTGCTTCCAAC[-/A]CTTGTTATTTGGTAA | 672 |
rs397507218 | in-del | C/GG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091759 | GTCTAAGAACACAGA[C/GG]AGAATTTATTATCAT | 672 |
rs397507219 | snp | C/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091749 | CAGAGGAGAATTTAT[C/G/T]ATCATTGAAGAATAG | 672 |
rs397507220 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091705 | AGTAACCAGGTAATA[-/A]TTGGCAAAGGCATCT | 672 |
rs397507221 | in-del | -/AC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091678 | TCTCAGGAACATCAC[-/AC]CTTAGTGAGGAAACA | 672 |
rs397507222 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091679 | ATCTCAGGAACATCA[-/C]CTTAGTGAGGAAACA | 672 |
rs397507223 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091654 | GAAACAAAATGTTCT[C/G]CTAGCTTGTTTTCTT | 672 |
rs397507224 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091540 | CATCAGTCTGAAAGC[C/T]AGGGAGTTGGTCTGA | 672 |
rs397507225 | snp | A/G | 1.64857e-05 | 0.00287099 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091458 | AAAATAATCAAGAAG[A/G]GCAAAGCATGGATTC | 672 |
rs397507226 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090948 | GTGACATTTTAACCA[C/T]TCAGGTAAAAAGCGT | 672 |
rs397507227 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082542 | CATAACCTGATAAAG[C/G]TCCAGCAGGAAATGG | 672 |
rs397507228 | snp | A/C | 1.64765e-05 | 0.00287019 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43104134 | ACAGAGTGAACCCGA[A/C]AATCCTTCCTTGGTA | 672 |
rs397507229 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076585 | CAGAAAAGTAGTGAA[-/T]ACCCTATAAGCCAGA | 672 |
rs397507230 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076579 | AGTAGTGAATACCCT[-/A]TAAGCCAGAATCCAG | 672 |
rs397507231 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076544 | CCTTTCTGCTGACAA[-/A]GTTTGAGGTGTCTGC | 672 |
rs397507232 | snp | A/T | 1.64784e-05 | 0.00287035 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43076516 | GCAGATAGTTCTACC[A/T]GTAAAAATAAAGAAC | 672 |
rs397507233 | snp | A/C | 0.000115307 | 0.00759211 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43099876 | ATACTGTTTAGCAGG[A/C]AACCAGTCTCAGTGT | 672 |
rs397507234 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074529 | TCTCCTTCCATTTAT[C/T]TTTCTAGGTCATCCC | 672 |
rs397507235 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074368 | GTCTGGGCCACACGA[G/T]TTGACGGAAACATCT | 672 |
rs397507236 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099855 | GTCTCAGTGTCCAAC[-/C]TCTCTAACCTTGGAA | 672 |
rs397507237 | in-del | ACATA/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071135 | CAGCTCGTGTTGGCA[ACATA/C]CCATCTTCAACCTCT | 672 |
rs397507238 | in-del | -/CCCCAATTGAAAGTT | 8.23621e-05 | 0.00641672 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43071093 | TCTGCATTGAAAGTT[-/CCCCAATTGAAAGTT]GCAGAATCTGCCCAG | 672 |
rs397507239 | snp | A/C/T | 8.25416e-05 | 0.00642371 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43067614 | ACTCATGTTGTTATG[A/C/T]AAACAGGTATACCAA | 672 |
rs397507240 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063957 | TGAGTGTTTTTCATT[A/C]TGCAGATGCTGAGTT | 672 |
rs397507241 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063936 | ATGCTGAGTTTGTGT[A/G]TGAACGGACACTGAA | 672 |
rs397507242 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063912 | CACTGAAATATTTTC[C/T]AGGAATTGCGGGAGG | 672 |
rs397507243 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063904 | TATTTTCTAGGAATT[A/G]CGGGAGGAAAATGGG | 672 |
rs397507244 | snp | A/G/T | | | missense, stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063335 | AGAAAAATGCTGAAT[A/G/T]AGGTAAGTACTTGAT | 672 |
rs397507245 | snp | A/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057087 | GGAAGAAACCACCAA[A/G/T]GTCCAAAGCGAGCAA | 672 |
rs397507246 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057063 | CGAGCAAGAGAATCC[-/C]CAGGACAGAAAGGTA | 672 |
rs397507247 | in-del | -/C | 0.000312935 | 0.0125048 | BRCA1 | 17 | allele_origin=C(germline)/+.-----(germline) | 17:43057062 | GAGCAAGAGAATCCC[-/C]AGGACAGAAAGGTAA | 672 |
rs397507248 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051105 | CAGATCTTCAGGGGG[-/G]CTAGAAATCTGTTGC | 672 |
rs397507249 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049141 | GTGGTGAAGGAGCTT[-/T]CATCATTCACCCTTG | 672 |
rs397507250 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099779 | GTCTGTCTACATTGA[A/G]TTGGGTAAGGGTCTC | 672 |
rs397507251 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097307 | TATTGATTTATTTTT[G/T]GGGGGGAAATTTTTT | 672 |
rs397507252 | snp | C/T | 1.65792e-05 | 0.00287912 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43097292 | TGGGGGGAAATTTTT[C/T]AGGATCTGATTCTTC | 672 |
rs397507253 | in-del | -/ACCCCAGAT | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045697 | GGACACCTACCTGAT[-/ACCCCAGAT]CCCCCACAGCCACTA | 672 |
rs397507254 | in-del | -/C | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045691 | TACCCCAGATCCCCC[-/C]ACAGCCACTACTGAC | 672 |
rs397507255 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045215 | GGAGAGTGCTTGGGA[-/T]CGATTATGTGACTTA | 672 |
rs397507256 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094786 | AATGATTTGAACACC[A/T]CTGAGAAGCGTGCAG | 672 |
rs397507257 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115779 | CCCCTACCCTGCTAG[-/T]CTGGAGTTGATCAAG | 672 |
rs397507258 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094575 | CAAGGAGCCAACATA[A/G]CAGATGGGCTGGAAG | 672 |
rs397507259 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094543 | AAGGAAACATGTAAT[A/G]ATAGGCGGACTCCCA | 672 |
rs397508826 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094519 | ACTCCCAGCACAGAA[A/T]AAAAGGTAGATCTGA | 672 |
rs397508827 | in-del | -/CT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094491 | CTGAATGCTGATCCC[-/CT]GTGTGAGAGAAAAGA | 672 |
rs397508828 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094491 | TGAATGCTGATCCCC[-/T]GTGTGAGAGAAAAGA | 672 |
rs397508829 | snp | A/C/T | 1.64749e-05 | 0.00287005 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43094468 | AGAAAAGAATGGAAT[A/C/T]AGCAGAAACTGCCAT | 672 |
rs397508830 | in-del | -/GAAACTGCCA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094454 | AGAATGGAATAAGCA[-/GAAACTGCCA]TGCTCAGAGAATCCT | 672 |
rs397508831 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094455 | ATAAGCAGAAACTGC[C/T]ATGCTCAGAGAATCC | 672 |
rs397508832 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094450 | CAGAAACTGCCATGC[-/A]TCAGAGAATCCTAGA | 672 |
rs397508833 | snp | C/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094449 | AGAAACTGCCATGCT[C/G]AGAGAATCCTAGAGA | 672 |
rs397508834 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094440 | CATGCTCAGAGAATC[-/C]TAGAGATACTGAAGA | 672 |
rs397508835 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094431 | AGAATCCTAGAGATA[-/A]CTGAAGATGTTCCTT | 672 |
rs397508836 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094430 | GAATCCTAGAGATAC[-/C]TGAAGATGTTCCTTG | 672 |
rs397508837 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094419 | ATACTGAAGATGTTC[-/C]TTGGATAACACTAAA | 672 |
rs397508838 | snp | A/G | 1.64762e-05 | 0.00287016 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094416 | CTGAAGATGTTCCTT[A/G]GATAACACTAAATAG | 672 |
rs397508839 | in-del | -/AC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094408 | TGTTCCTTGGATAAC[-/AC]TAAATAGCAGCATTC | 672 |
rs397508840 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094393 | CTAAATAGCAGCATT[C/T]AGAAAGTTAATGAGT | 672 |
rs397508841 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094378 | CAGAAAGTTAATGAG[-/G]TGGTTTTCCAGAAGT | 672 |
rs397508842 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094372 | AGTTAATGAGTGGTT[-/TT]CCAGAAGTGATGAAC | 672 |
rs397508843 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094371 | TTAATGAGTGGTTTT[-/T]CCAGAAGTGATGAAC | 672 |
rs397508844 | in-del | -/TGTT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094353 | CCAGAAGTGATGAAC[-/TGTT]AGGTTCTGATGACTC | 672 |
rs397508845 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094343 | ACTGTTAGGTTCTGA[-/T]GACTCACATGATGGG | 672 |
rs397508846 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094314 | GGGAGTCTGAATCAA[-/A]TGCCAAAGTAGCTGA | 672 |
rs397508847 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115738 | CCACAAAGTGTGACC[-/A]CATATTTTGCAAGTA | 672 |
rs397508848 | in-del | -/AT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094298 | ATGCCAAAGTAGCTG[-/AT]GTATTGGACGTTCTA | 672 |
rs397508849 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094269 | TAAATGAGGTAGATG[A/G]ATATTCTGGTTCTTC | 672 |
rs397508850 | in-del | -/AT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094264 | GAGGTAGATGAATAT[-/AT]TCTGGTTCTTCAGAG | 672 |
rs397508851 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094252 | TATTCTGGTTCTTCA[G/T]AGAAAATAGACTTAC | 672 |
rs397508852 | in-del | ACT/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094236 | AGAGAAAATAGACTT[ACT/GA]GGCCAGTGATCCTCA | 672 |
rs397508853 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094211 | TCCTCATGAGGCTTT[-/T]AATATGTAAAAGTGA | 672 |
rs397508854 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094205 | TGAGGCTTTAATATG[A/T]AAAAGTGAAAGAGTT | 672 |
rs397508855 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094191 | GTAAAAGTGAAAGAG[-/G]TTCACTCCAAATCAG | 672 |
rs397508856 | in-del | AAGTA/T | | | intron-variant, splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43115723 | GACCACATATTTTGC[AAGTA/T]AGTTTGAATGTGTTA | 672 |
rs397508857 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115726 | GACCACATATTTTGC[-/AA]GTAAGTTTGAATGTG | 672 |
rs397508858 | in-del | -/AAGT | 1.82115e-05 | 0.00301751 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43115720 | ACATATTTTGCAAGT[-/AAGT]TTGAATGTGTTATGT | 672 |
rs397508859 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106539 | TTCTTTCTTTATAAT[G/T]TATAGATTTTGCATG | 672 |
rs397508860 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094167 | AATCAGTAGAGAGTA[-/GA]ATATTGAAGACAAAA | 672 |
rs397508861 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094160 | AGAGAGTAATATTGA[-/A]GACAAAATATTTGGG | 672 |
rs397508862 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094157 | GAGTAATATTGAAGA[-/C]AAAATATTTGGGAAA | 672 |
rs397508863 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094151 | TATTGAAGACAAAAT[-/A]TTTGGGAAAACCTAT | 672 |
rs397508864 | in-del | -/GGGAAAACCT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094137 | TATTTGGGAAAACCT[-/GGGAAAACCT]ATCGGAAGAAGGCAA | 672 |
rs397508865 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094144 | GACAAAATATTTGGG[-/G]AAAACCTATCGGAAG | 672 |
rs397508866 | in-del | AAAA/GAAAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094141 | GACAAAATATTTGGG[AAAA/GAAAG]CCTATCGGAAGAAGG | 672 |
rs397508867 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094140 | AAATATTTGGGAAAA[-/G]CCTATCGGAAGAAGG | 672 |
rs397508868 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094139 | AATATTTGGGAAAAC[-/C]TATCGGAAGAAGGCA | 672 |
rs397508869 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094138 | ATATTTGGGAAAACC[G/T]ATCGGAAGAAGGCAA | 672 |
rs397508870 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094128 | AAACCTATCGGAAGA[-/A]GGCAAGCCTCCCCAA | 672 |
rs397508871 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094126 | ACCTATCGGAAGAAG[-/G]CAAGCCTCCCCAACT | 672 |
rs397508872 | in-del | -/GAGCGTCCCCTCACAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094033 | CCACAGATAATACAA[-/GAGCGTCCCCTCACAA]ATAAATTAAAGCGTA | 672 |
rs397508873 | in-del | -/ATAAATTAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094022 | CACAAATAAATTAAA[-/ATAAATTAAA]GCGTAAAAGGAGACC | 672 |
rs397508874 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094032 | AGCGTCCCCTCACAA[-/A]TAAATTAAAGCGTAA | 672 |
rs397508875 | in-del | -/TTAAAGCGTAAAAGG | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094013 | CCCCTCACAAATAAA[-/TTAAAGCGTAAAAGG]AGACCTACATCAGGC | 672 |
rs397508876 | in-del | -/AAAGC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094021 | CCTCACAAATAAATT[-/AAAGC]GTAAAAGGAGACCTA | 672 |
rs397508877 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094018 | AATAAATTAAAGCGT[A/T]AAAGGAGACCTACAT | 672 |
rs397508878 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094017 | ATAAATTAAAGCGTA[-/T]AAAGGAGACCTACAT | 672 |
rs397508879 | in-del | -/GGAGA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094010 | AATTAAAGCGTAAAA[-/GGAGA]CCTACATCAGGCCTT | 672 |
rs397508880 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094012 | TTAAAGCGTAAAAGG[A/T]GACCTACATCAGGCC | 672 |
rs397508881 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093987 | CAGGCCTTCATCCTG[A/G]GGATTTTATCAAGAA | 672 |
rs397508882 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093976 | CCTGAGGATTTTATC[A/C]AGAAAGCAGATTTGG | 672 |
rs397508883 | multinucleotide-polymorphism | GCAG/TAAA | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093967 | GATTTTATCAAGAAA[GCAG/TAAA]ATTTGGCAGTTCAAA | 672 |
rs397508884 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093965 | TATCAAGAAAGCAGA[-/C]TTTGGCAGTTCAAAA | 672 |
rs397508885 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093963 | TCAAGAAAGCAGATT[G/T]GGCAGTTCAAAAGAC | 672 |
rs397508886 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093961 | AAGAAAGCAGATTTG[-/G]CAGTTCAAAAGACTC | 672 |
rs397508887 | in-del | -/CTCCTGA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093942 | TGGCAGTTCAAAAGA[-/CTCCTGA]AATGATAAATCAGGG | 672 |
rs397508888 | in-del | -/TAAATCA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093930 | AGACTCCTGAAATGA[-/TAAATCA]GGGAACTAACCAAAC | 672 |
rs397508889 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093929 | TGAAATGATAAATCA[-/A]GGGAACTAACCAAAC | 672 |
rs397508890 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106508 | CTGAAACTTCTCAAC[-/C]AGAAGAAAGGGCCTT | 672 |
rs397508891 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093907 | AACCAAACGGAGCAG[-/G]AATGGTCAAGTGATG | 672 |
rs397508892 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093900 | CGGAGCAGAATGGTC[A/C]AGTGATGAATATTAC | 672 |
rs397508893 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093876 | ATATTACTAATAGTG[G/T]TCATGAGAATAAAAC | 672 |
rs397508894 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093871 | ACTAATAGTGGTCAT[G/T]AGAATAAAACAAAAG | 672 |
rs397508895 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093862 | GGTCATGAGAATAAA[A/G]CAAAAGGTGATTCTA | 672 |
rs397508896 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093857 | ATGAGAATAAAACAA[-/AA]GGTGATTCTATTCAG | 672 |
rs397508897 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106501 | TTCTCAACCAGAAGA[A/G]AGGGCCTTCACAGTG | 672 |
rs397508898 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106500 | TCTCAACCAGAAGAA[A/T]GGGCCTTCACAGTGT | 672 |
rs397508899 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093831 | TTCAGAATGAGAAAA[-/A]TCCTAACCCAATAGA | 672 |
rs397508900 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093815 | TCCTAACCCAATAGA[-/A]TCACTCGAAAAAGAA | 672 |
rs397508901 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093814 | CCTAACCCAATAGAA[-/A]TCACTCGAAAAAGAA | 672 |
rs397508902 | snp | A/G | 3.30246e-05 | 0.0040634 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093808 | CCAATAGAATCACTC[A/G]AAAAAGAATCTGCTT | 672 |
rs397508903 | snp | C/G/T | 1.65111e-05 | 0.0028732 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43093802 | GAATCACTCGAAAAA[C/G/T]AATCTGCTTTCAAAA | 672 |
rs397508904 | snp | A/C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106496 | AACCAGAAGAAAGGG[A/C/G]CTTCACAGTGTCCTT | 672 |
rs397508905 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093790 | AAAGAATCTGCTTTC[A/T]AAACGAAAGCTGAAC | 672 |
rs397508906 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093787 | GAATCTGCTTTCAAA[A/G]CGAAAGCTGAACCTA | 672 |
rs397508907 | in-del | -/CA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106489 | AAGAAAGGGCCTTCA[-/CA]GTGTCCTTTATGTAA | 672 |
rs397508908 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093726 | AATTAAATATCCACA[-/A]TTCAAAAGCACCTAA | 672 |
rs397508909 | snp | C/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093723 | TAAATATCCACAATT[C/G]AAAAGCACCTAAAAA | 672 |
rs397508910 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093714 | ACAATTCAAAAGCAC[-/C]TAAAAAGAATAGGCT | 672 |
rs397508911 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093708 | CAAAAGCACCTAAAA[-/A]GAATAGGCTGAGGAG | 672 |
rs397508912 | in-del | -/GT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106485 | AAGGGCCTTCACAGT[-/GT]CCTTTATGTAAGAAT | 672 |
rs397508913 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093700 | CCTAAAAAGAATAGG[-/C]TGAGGAGGAAGTCTT | 672 |
rs397508914 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093684 | TGAGGAGGAAGTCTT[-/T]CTACCAGGCATATTC | 672 |
rs397508915 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093663 | GGCATATTCATGCGC[C/T]TGAACTAGTAGTCAG | 672 |
rs397508916 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093625 | CTAAGCCCACCTAAT[-/T]GTACTGAATTGCAAA | 672 |
rs397508917 | in-del | -/TGTA | | | frameshift-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43106475 | TCACAGTGTCCTTTA[-/TGTA]AGAATGATATAACCA | 672 |
rs397508918 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093599 | GCAAATTGATAGTTG[G/T]TCTAGCAGTGAAGAG | 672 |
rs397508919 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093595 | ATTGATAGTTGTTCT[-/A]GCAGTGAAGAGATAA | 672 |
rs397508920 | in-del | -/CAGTGAAGAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093584 | TGATAGTTGTTCTAG[-/CAGTGAAGAG]ATAAAGAAAAAAAAG | 672 |
rs397508921 | in-del | -/TA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093581 | CTAGCAGTGAAGAGA[-/TA]AAGAAAAAAAAGTAC | 672 |
rs397508922 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093579 | GCAGTGAAGAGATAA[-/A]GAAAAAAAAGTACAA | 672 |
rs397508923 | in-del | -/AAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093570 | AAGAGATAAAGAAAA[-/AAAA]GTACAACCAAATGCC | 672 |
rs397508924 | in-del | -/G/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093567 | TAAAGAAAAAAAAGT[-/G/T]ACAACCAAATGCCAG | 672 |
rs397508925 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093564 | AGAAAAAAAAGTACA[A/G]CCAAATGCCAGTCAG | 672 |
rs397508926 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093562 | AAAAAAAAGTACAAC[C/T]AAATGCCAGTCAGGC | 672 |
rs397508927 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093547 | CAAATGCCAGTCAGG[C/T]ACAGCAGAAACCTAC | 672 |
rs397508928 | in-del | -/GT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093517 | CAACTCATGGAAGGT[-/GT]AAAGAACCTGCAACT | 672 |
rs397508929 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093517 | CAACTCATGGAAGGT[A/G/T]AAGAACCTGCAACTG | 672 |
rs397508930 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093510 | TGGAAGGTAAAGAAC[-/C]TGCAACTGGAGCCAA | 672 |
rs397508931 | in-del | -/TG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093502 | TAAAGAACCTGCAAC[-/TG]GAGCCAAGAAGAGTA | 672 |
rs397508932 | in-del | CC/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093494 | TGCAACTGGAGCCAA[CC/G]AAGAGTAACAAGCCA | 672 |
rs397508933 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093483 | CCAAGAAGAGTAACA[-/A]GCCAAATGAACAGAC | 672 |
rs397508934 | snp | A/C/T | 1.64792e-05 | 0.00287042 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43093481 | AAGAAGAGTAACAAG[A/C/T]CAAATGAACAGACAA | 672 |
rs397508935 | in-del | -/CAAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093465 | AGCCAAATGAACAGA[-/CAAG]TAAAAGACATGACAG | 672 |
rs397508936 | in-del | -/AT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093455 | AGACAAGTAAAAGAC[-/AT]GACAGCGATACTTTC | 672 |
rs397508937 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093445 | AGACATGACAGCGAT[-/A]CTTTCCCAGAGCTGA | 672 |
rs397508938 | in-del | -/A | | | frameshift-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43106456 | ATGATATAACCAAAA[-/A]GGTATATAATTTGGT | 672 |
rs397508939 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093404 | ATGCACCTGGTTCTT[-/TT]ACTAAGTGTTCAAAT | 672 |
rs397508940 | snp | A/C | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43104958 | AAACAATTTAATTTC[A/C]GGAGCCTACAAGAAA | 672 |
rs397508941 | in-del | -/AAAGAATTTGTCAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093363 | AATACCAGTGAACTT[-/AAAGAATTTGTCAA]TCCTAGCCTTCCAAG | 672 |
rs397508942 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093373 | ACCAGTGAACTTAAA[-/A]GAATTTGTCAATCCT | 672 |
rs397508943 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093365 | ACTTAAAGAATTTGT[-/C]AATCCTAGCCTTCCA | 672 |
rs397508944 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093357 | AATTTGTCAATCCTA[-/G]CCTTCCAAGAGAAGA | 672 |
rs397508945 | in-del | -/CT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093354 | TTTGTCAATCCTAGC[-/CT]TCCAAGAGAAGAAAA | 672 |
rs397508946 | in-del | -/AAGAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093335 | TTCCAAGAGAAGAAA[-/AAGAA]GAGAAACTAGAAACA | 672 |
rs397508947 | in-del | -/AGAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093335 | TCCAAGAGAAGAAAA[-/AGAA]GAGAAACTAGAAACA | 672 |
rs397508948 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093335 | AAGAGAAGAAAAAGA[-/A]GAGAAACTAGAAACA | 672 |
rs397508949 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093334 | AGAGAAGAAAAAGAA[G/T]AGAAACTAGAAACAG | 672 |
rs397508950 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093319 | AGAGAAACTAGAAAC[-/AG]TTAAAGTGTCTAATA | 672 |
rs397508951 | in-del | -/GTTA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093316 | GAGAAACTAGAAACA[-/GTTA]AAGTGTCTAATAATG | 672 |
rs397508952 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093314 | AACTAGAAACAGTTA[-/AA]GTGTCTAATAATGCT | 672 |
rs397508953 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093289 | AATGCTGAAGACCCC[-/C]AAAGATCTCATGTTA | 672 |
rs397508954 | in-del | -/CTCAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093279 | GAAGACCCCAAAGAT[-/CTCAT]GTTAAGTGGAGAAAG | 672 |
rs397508955 | in-del | -/AGAGAGTAGCAGTATTTCA/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093220 | AGTAGCAGTATTTCA[-/AGAGAGTAGCAGTATTTCA/C]TTGGTACCTGGTACT | 672 |
rs397508956 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093223 | GAGAGTAGCAGTATT[-/T]CATTGGTACCTGGTA | 672 |
rs397508957 | in-del | C/GTCAACTTGTT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104939 | GCCTACAAGAAAGTA[C/GTCAACTTGTT]GAGATTTAGTCAACT | 672 |
rs397508958 | snp | A/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093209 | TTCATTGGTACCTGG[A/T]ACTGATTATGGCACT | 672 |
rs397508959 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093205 | TTGGTACCTGGTACT[-/A]GATTATGGCACTCAG | 672 |
rs397508960 | in-del | -/TC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093180 | ACTCAGGAAAGTATC[-/TC]GTTACTGGAAGTTAG | 672 |
rs397508961 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093177 | AGGAAAGTATCTCGT[A/T]ACTGGAAGTTAGCAC | 672 |
rs397508962 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093175 | GAAAGTATCTCGTTA[-/C]TGGAAGTTAGCACTC | 672 |
rs397508963 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093174 | AAAGTATCTCGTTAC[-/T]GGAAGTTAGCACTCT | 672 |
rs397508964 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093172 | AGTATCTCGTTACTG[-/G]AAGTTAGCACTCTAG | 672 |
rs397508965 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093142 | GGGAAGGCAAAAACA[-/G]AACCAAATAAATGTG | 672 |
rs397508966 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093118 | AAATGTGTGAGTCAG[C/T]GTGCAGCATTTGAAA | 672 |
rs397508967 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093102 | GTGCAGCATTTGAAA[-/A]CCCCAAGGGACTAAT | 672 |
rs397508968 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093097 | GCATTTGAAAACCCC[A/T]AGGGACTAATTCATG | 672 |
rs397508969 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093090 | AAAACCCCAAGGGAC[-/A]TAATTCATGGTTGTT | 672 |
rs397508970 | snp | A/C | 1.64787e-05 | 0.00287038 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43093050 | TAGAAATGACACAGA[A/C]GGCTTTAAGTATCCA | 672 |
rs397508971 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093044 | ATGACACAGAAGGCT[-/TT]AAGTATCCATTGGGA | 672 |
rs397508972 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093043 | GACACAGAAGGCTTT[-/T]AAGTATCCATTGGGA | 672 |
rs397508973 | in-del | -/AAGTATCCAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093033 | GCTTTAAGTATCCAT[-/AAGTATCCAT]TGGGACATGAAGTTA | 672 |
rs397508974 | in-del | -/CA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093013 | ACATGAAGTTAACCA[-/CA]GTCGGGAAACAAGCA | 672 |
rs397508975 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093013 | CATGAAGTTAACCAC[-/A]GTCGGGAAACAAGCA | 672 |
rs397508976 | snp | C/T | 1.64838e-05 | 0.00287083 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092997 | GTCGGGAAACAAGCA[C/T]AGAAATGGAAGAAAG | 672 |
rs397508977 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092980 | GAAATGGAAGAAAGT[-/G]AACTTGATGCTCAGT | 672 |
rs397508978 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092975 | GGAAGAAAGTGAACT[-/T]GATGCTCAGTATTTG | 672 |
rs397508979 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092974 | GAAGAAAGTGAACTT[-/T]GATGCTCAGTATTTG | 672 |
rs397508980 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092972 | AGAAAGTGAACTTGA[-/A]TGCTCAGTATTTGCA | 672 |
rs397508981 | in-del | -/CTCAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092966 | AAAGTGAACTTGATG[-/CTCAG]TATTTGCAGAATACA | 672 |
rs397508982 | in-del | -/TTGAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092966 | TGAACTTGATGCTCA[-/TTGAT]GTATTTGCAGAATAC | 672 |
rs397508983 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092959 | GATGCTCAGTATTTG[C/T]AGAATACATTCAAGG | 672 |
rs397508984 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092937 | CATTCAAGGTTTCAA[-/A]GCGCCAGTCATTTGC | 672 |
rs397508985 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092931 | AGGTTTCAAAGCGCC[A/G]GTCATTTGCTCCGTT | 672 |
rs397508986 | in-del | C/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092919 | GCCAGTCATTTGCTC[C/TT]GTTTTCAAATCCAGG | 672 |
rs397508987 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092913 | CATTTGCTCCGTTTT[-/T]CAAATCCAGGAAATG | 672 |
rs397508988 | snp | A/G/T | 1.64781e-05 | 0.00287033 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43092890 | GGAAATGCAGAAGAG[A/G/T]AATGTGCAACATTCT | 672 |
rs397508989 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092888 | AAATGCAGAAGAGGA[-/A]TGTGCAACATTCTCT | 672 |
rs397508990 | in-del | -/CT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092873 | AATGTGCAACATTCT[-/CT]GCCCACTCTGGGTCC | 672 |
rs397508991 | in-del | -/A/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092871 | GTGCAACATTCTCTG[-/A/G]CCCACTCTGGGTCCT | 672 |
rs397508992 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092865 | CATTCTCTGCCCACT[-/T]CTGGGTCCTTAAAGA | 672 |
rs397508993 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092860 | TCTGCCCACTCTGGG[-/T]CCTTAAAGAAACAAA | 672 |
rs397508994 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092856 | CCCACTCTGGGTCCT[C/T]AAAGAAACAAAGTCC | 672 |
rs397508995 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092851 | CTCTGGGTCCTTAAA[-/GA]AACAAAGTCCAAAAG | 672 |
rs397508996 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092849 | TGGGTCCTTAAAGAA[-/A]CAAAGTCCAAAAGTC | 672 |
rs397508997 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092848 | GGGTCCTTAAAGAAA[C/T]AAAGTCCAAAAGTCA | 672 |
rs397508998 | in-del | -/CAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092845 | GGGTCCTTAAAGAAA[-/CAAA]GTCCAAAAGTCACTT | 672 |
rs397508999 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092841 | TAAAGAAACAAAGTC[-/A]CAAAAGTCACTTTTG | 672 |
rs397509000 | in-del | -/A/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092836 | AAACAAAGTCCAAAA[-/A/AA]GTCACTTTTGAATGT | 672 |
rs397509001 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092828 | GTCCAAAAGTCACTT[-/TT]GAATGTGAACAAAAG | 672 |
rs397509002 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092818 | ACTTTTGAATGTGAA[C/T]AAAAGGAAGAAAATC | 672 |
rs397509003 | in-del | -/ATCAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092801 | AACAAAAGGAAGAAA[-/ATCAA]GGAAAGAATGAGTCT | 672 |
rs397509004 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092803 | CAAAAGGAAGAAAAT[C/T]AAGGAAAGAATGAGT | 672 |
rs397509005 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092803 | CAAAAGGAAGAAAAT[-/C]AAGGAAAGAATGAGT | 672 |
rs397509006 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104896 | ATTGAAAATCATTTG[G/T]GCTTTTCAGCTTGAC | 672 |
rs397509007 | in-del | -/CT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092786 | AAGGAAAGAATGAGT[-/CT]AATATCAAGCCTGTA | 672 |
rs397509008 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092785 | GGAAAGAATGAGTCT[-/T]AATATCAAGCCTGTA | 672 |
rs397509009 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092781 | AGAATGAGTCTAATA[-/A]TCAAGCCTGTACAGA | 672 |
rs397509010 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092779 | AATGAGTCTAATATC[A/C]AGCCTGTACAGACAG | 672 |
rs397509011 | in-del | -/GT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092732 | GCTTTCCTGTGGTTG[-/GT]CAGAAAGATAAGCCA | 672 |
rs397509012 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092726 | TGTGGTTGGTCAGAA[-/A]GATAAGCCAGTTGAT | 672 |
rs397509013 | in-del | -/TAAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092720 | GGTTGGTCAGAAAGA[-/TAAG]CCAGTTGATAATGCC | 672 |
rs397509014 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092701 | GTTGATAATGCCAAA[-/T]GTAGTATCAAAGGAG | 672 |
rs397509015 | in-del | -/GT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092696 | ATAATGCCAAATGTA[-/GT]ATCAAAGGAGGCTCT | 672 |
rs397509016 | in-del | -/AT | 1.64773e-05 | 0.00287026 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43092694 | AATGCCAAATGTAGT[-/AT]CAAAGGAGGCTCTAG | 672 |
rs397509017 | in-del | -/AGGCTCTAGG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092678 | ATGTAGTATCAAAGG[-/AGGCTCTAGG]TTTTGTCTATCATCT | 672 |
rs397509018 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092682 | GTATCAAAGGAGGCT[-/T]CTAGGTTTTGTCTAT | 672 |
rs397509019 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092674 | AGGAGGCTCTAGGTT[-/TT]GTCTATCATCTCAGT | 672 |
rs397509020 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092660 | TTGTCTATCATCTCA[-/A]GTTCAGAGGCAACGA | 672 |
rs397509021 | in-del | -/TTCAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092655 | TGTCTATCATCTCAG[-/TTCAG]AGGCAACGAAACTGG | 672 |
rs397509022 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092652 | CATCTCAGTTCAGAG[A/G]CAACGAAACTGGACT | 672 |
rs397509023 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092617 | ACTCCAAATAAACAT[G/T]GACTTTTACAAAACC | 672 |
rs397509024 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092609 | TAAACATGGACTTTT[-/T]ACAAAACCCATATCG | 672 |
rs397509025 | in-del | -/CC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092600 | ACTTTTACAAAACCC[-/CC]ATATCGTATACCACC | 672 |
rs397509026 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092578 | ATACCACCACTTTTT[-/T]CCCATCAAGTCATTT | 672 |
rs397509027 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092576 | ACCACCACTTTTTCC[-/C]ATCAAGTCATTTGTT | 672 |
rs397509028 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092564 | TCCCATCAAGTCATT[-/T]GTTAAAACTAAATGT | 672 |
rs397509029 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092563 | CCCATCAAGTCATTT[A/G]TTAAAACTAAATGTA | 672 |
rs397509030 | in-del | -/AACTAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092552 | CAAGTCATTTGTTAA[-/AACTAAA]TGTAAGAAAAATCTG | 672 |
rs397509031 | in-del | -/ACTAAATGTAAGAAAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092541 | AAGTCATTTGTTAAA[-/ACTAAATGTAAGAAAAA]TCTGCTAGAGGAAAA | 672 |
rs397509032 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092541 | CTAAATGTAAGAAAA[-/A]TCTGCTAGAGGAAAA | 672 |
rs397509033 | snp | A/C/G | 1.64811e-05 | 0.00287059 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43092459 | TCCAAGTACAGTGAG[A/C/G]ACAATTAGCCGTAAT | 672 |
rs397509034 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092457 | CAAGTACAGTGAGCA[C/T]AATTAGCCGTAATAA | 672 |
rs397509035 | snp | C/G | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092409 | TTAAAGAAGCCAGCT[C/G]AAGCAATATTAATGA | 672 |
rs397509036 | in-del | -/GCAATATTAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092397 | AAGAAGCCAGCTCAA[-/GCAATATTAA]TGAAGTAGGTTCCAG | 672 |
rs397509037 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092391 | GCAATATTAATGAAG[C/T]AGGTTCCAGTACTAA | 672 |
rs397509038 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092386 | ATTAATGAAGTAGGT[-/T]CCAGTACTAATGAAG | 672 |
rs397509039 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092379 | AAGTAGGTTCCAGTA[C/G]TAATGAAGTGGGCTC | 672 |
rs397509040 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092376 | TAGGTTCCAGTACTA[-/A]TGAAGTGGGCTCCAG | 672 |
rs397509041 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092374 | GGTTCCAGTACTAAT[-/G]AAGTGGGCTCCAGTA | 672 |
rs397509042 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092373 | GTTCCAGTACTAATG[-/G]AAGTGGGCTCCAGTA | 672 |
rs397509043 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092367 | GTACTAATGAAGTGG[-/G]CTCCAGTATTAATGA | 672 |
rs397509044 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092363 | TAATGAAGTGGGCTC[-/C]AGTATTAATGAAATA | 672 |
rs397509045 | in-del | -/AGTA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092359 | AATGAAGTGGGCTCC[-/AGTA]TTAATGAAATAGGTT | 672 |
rs397509046 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092348 | CAGTATTAATGAAAT[-/A]GGTTCCAGTGATGAA | 672 |
rs397509047 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092319 | AAAACATTCAAGCAG[-/G]AACTAGGTAGAAACA | 672 |
rs397509048 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092303 | ACTAGGTAGAAACAG[A/T]GGGCCAAAATTGAAT | 672 |
rs397509049 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092269 | ATGCTTAGATTAGGG[-/G]TTTTGCAACCTGAGG | 672 |
rs397509050 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092252 | TTTGCAACCTGAGGT[-/C]TATAAACAAAGTCTT | 672 |
rs397509051 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092246 | ACCTGAGGTCTATAA[-/A]CAAAGTCTTCCTGGA | 672 |
rs397509052 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092242 | GAGGTCTATAAACAA[-/A]GTCTTCCTGGAAGTA | 672 |
rs397509053 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104234 | ATAATTTTGCAAAAA[A/C]GGAAAATAACTCTCC | 672 |
rs397509054 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092217 | GAAGTAATTGTAAGC[-/A]TCCTGAAATAAAAAA | 672 |
rs397509055 | in-del | -/TAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092205 | GTAAGCATCCTGAAA[-/TAAA]AAAGCAAGAATATGA | 672 |
rs397509056 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092202 | ATCCTGAAATAAAAA[-/A]GCAAGAATATGAAGA | 672 |
rs397509057 | in-del | -/AGAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092195 | TGAAATAAAAAAGCA[-/AGAA]TATGAAGAAGTAGTT | 672 |
rs397509058 | in-del | -/AGAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092186 | AAAGCAAGAATATGA[-/AGAA]GTAGTTCAGACTGTT | 672 |
rs397509059 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092176 | TGAAGAAGTAGTTCA[-/GA]CTGTTAATACAGATT | 672 |
rs397509060 | in-del | -/TTAAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092168 | AAGTAGTTCAGACTG[-/TTAAT]ACAGATTTCTCTCCA | 672 |
rs397509061 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092154 | ATACAGATTTCTCTC[-/C]ATATCTGATTTCAGA | 672 |
rs397509062 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104223 | AAAAAGGAAAATAAC[C/T]CTCCTGAACATCTAA | 672 |
rs397509063 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092118 | TAGAACAGCCTATGG[-/G]AAGTAGTCATGCATC | 672 |
rs397509064 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092115 | AACAGCCTATGGGAA[-/G]TAGTCATGCATCTCA | 672 |
rs397509065 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092110 | CCTATGGGAAGTAGT[-/T]CATGCATCTCAGGTT | 672 |
rs397509066 | in-del | C/TA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092103 | GAAGTAGTCATGCAT[C/TA]TCAGGTTTGTTCTGA | 672 |
rs397509067 | in-del | -/TGTT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092092 | CATGCATCTCAGGTT[-/TGTT]CTGAGACACCTGATG | 672 |
rs397509068 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092081 | TTGTTCTGAGACACC[-/T]GATGACCTGTTAGAT | 672 |
rs397509069 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092080 | TGTTCTGAGACACCT[-/T]GATGACCTGTTAGAT | 672 |
rs397509070 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092063 | TGACCTGTTAGATGA[-/T]GGTGAAATAAAGGAA | 672 |
rs397509071 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104217 | GAAAATAACTCTCCT[A/G]AACATCTAAAAGATG | 672 |
rs397509072 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092059 | CTGTTAGATGATGGT[G/T]AAATAAAGGAAGATA | 672 |
rs397509073 | in-del | -/AGGAAGATAC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092043 | ATGATGGTGAAATAA[-/AGGAAGATAC]TAGTTTTGCTGAAAA | 672 |
rs397509074 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092050 | GATGGTGAAATAAAG[-/G]AAGATACTAGTTTTG | 672 |
rs397509075 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092040 | TAAAGGAAGATACTA[G/T]TTTTGCTGAAAATGA | 672 |
rs397509076 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092036 | AGGAAGATACTAGTT[-/TT]GCTGAAAATGACATT | 672 |
rs397509077 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092027 | TAGTTTTGCTGAAAA[-/A]TGACATTAAGGAAAG | 672 |
rs397509078 | in-del | -/GACAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092022 | AGTTTTGCTGAAAAT[-/GACAT]TAAGGAAAGTTCTGC | 672 |
rs397509079 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092017 | GAAAATGACATTAAG[G/T]AAAGTTCTGCTGTTT | 672 |
rs397509080 | in-del | -/CG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091990 | TGTTTTTAGCAAAAG[-/CG]TCCAGAAAGGAGAGC | 672 |
rs397509081 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091978 | AGCGTCCAGAAAGGA[G/T]AGCTTAGCAGGAGTC | 672 |
rs397509082 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091955 | CAGGAGTCCTAGCCC[-/AA]TTTCACCCATACACA | 672 |
rs397509083 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091952 | GAGTCCTAGCCCTTT[-/T]CACCCATACACATTT | 672 |
rs397509084 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091948 | CCTAGCCCTTTCACC[-/C]ATACACATTTGGCTC | 672 |
rs397509085 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091938 | TCACCCATACACATT[A/T]GGCTCAGGGTTACCG | 672 |
rs397509086 | in-del | -/CTCAGGG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091929 | CCCATACACATTTGG[-/CTCAGGG]TTACCGAAGAGGGGC | 672 |
rs397509087 | in-del | AA/GAAATT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091905 | CCGAAGAGGGGCCAA[AA/GAAATT]AGAGTCCTCAGAAGA | 672 |
rs397509088 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091906 | AGAGGGGCCAAGAAA[-/A]TTAGAGTCCTCAGAA | 672 |
rs397509089 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091904 | AGGGGCCAAGAAATT[-/T]AGAGTCCTCAGAAGA | 672 |
rs397509090 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091903 | GGGGCCAAGAAATTA[-/G]AGTCCTCAGAAGAGA | 672 |
rs397509091 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091884 | CCTCAGAAGAGAACT[G/T]ATCTAGTGAGGATGA | 672 |
rs397509092 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091837 | CAACACTTGTTATTT[-/T]GGTAAAGTAAACAAT | 672 |
rs397509093 | in-del | -/GTAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091833 | AACACTTGTTATTTG[-/GTAA]AGTAAACAATATACC | 672 |
rs397509094 | in-del | -/ACAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091824 | TATTTGGTAAAGTAA[-/ACAA]TATACCTTCTCAGTC | 672 |
rs397509095 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091827 | TATTTGGTAAAGTAA[-/A]CAATATACCTTCTCA | 672 |
rs397509096 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091816 | GTAAACAATATACCT[-/T]CTCAGTCTACTAGGC | 672 |
rs397509097 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091814 | AAACAATATACCTTC[-/C]TCAGTCTACTAGGCA | 672 |
rs397509098 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091778 | CGTTGCTACCGAGTG[A/T]CTGTCTAAGAACACA | 672 |
rs397509099 | in-del | -/GT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091774 | TGCTACCGAGTGTCT[-/GT]CTAAGAACACAGAGG | 672 |
rs397509100 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091773 | CTACCGAGTGTCTGT[A/C/G]TAAGAACACAGAGGA | 672 |
rs397509101 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104187 | GAAGTTTCTATCATC[-/T]CAAAGTATGGGCTAC | 672 |
rs397509102 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091768 | CGAGTGTCTGTCTAA[-/GA]ACACAGAGGAGAATT | 672 |
rs397509103 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091767 | GAGTGTCTGTCTAAG[-/AA]CACAGAGGAGAATTT | 672 |
rs397509104 | in-del | -/GGAGAATT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091753 | GTCTAAGAACACAGA[-/GGAGAATT]TATTATCATTGAAGA | 672 |
rs397509105 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091759 | TCTAAGAACACAGAG[G/T]AGAATTTATTATCAT | 672 |
rs397509106 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091756 | TAAGAACACAGAGGA[-/GA]ATTTATTATCATTGA | 672 |
rs397509107 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091752 | ACACAGAGGAGAATT[-/T]ATTATCATTGAAGAA | 672 |
rs397509108 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091717 | TTAAATGACTGCAGT[-/T]AACCAGGTAATATTG | 672 |
rs397509109 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091716 | TAAATGACTGCAGTA[-/T]ACCAGGTAATATTGG | 672 |
rs397509110 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091711 | GACTGCAGTAACCAG[-/G]TAATATTGGCAAAGG | 672 |
rs397509111 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091708 | TGCAGTAACCAGGTA[-/T]ATATTGGCAAAGGCA | 672 |
rs397509112 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091702 | AACCAGGTAATATTG[C/G]CAAAGGCATCTCAGG | 672 |
rs397509113 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091687 | GCAAAGGCATCTCAG[-/G]AACATCACCTTAGTG | 672 |
rs397509114 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091659 | GTGAGGAAACAAAAT[-/C]GTTCTGCTAGCTTGT | 672 |
rs397509115 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091655 | GGAAACAAAATGTTC[-/T]GCTAGCTTGTTTTCT | 672 |
rs397509116 | in-del | -/AGCT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091648 | ACAAAATGTTCTGCT[-/AGCT]TGTTTTCTTCACAGT | 672 |
rs397509117 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091621 | CAGTGCAGTGAATTG[-/G]AAGACTTGACTGCAA | 672 |
rs397509118 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091617 | GCAGTGAATTGGAAG[-/A]CTTGACTGCAAATAC | 672 |
rs397509119 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091605 | AAGACTTGACTGCAA[-/A]TACAAACACCCAGGA | 672 |
rs397509120 | in-del | -/TACA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091601 | AGACTTGACTGCAAA[-/TACA]AACACCCAGGATCCT | 672 |
rs397509121 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091579 | CAGGATCCTTTCTTG[A/G]TTGGTTCTTCCAAAC | 672 |
rs397509122 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091564 | ATTGGTTCTTCCAAA[-/C]AAATGAGGCATCAGT | 672 |
rs397509123 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091550 | ACAAATGAGGCATCA[-/G]TCTGAAAGCCAGGGA | 672 |
rs397509124 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091548 | AAATGAGGCATCAGT[-/T]CTGAAAGCCAGGGAG | 672 |
rs397509125 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091532 | TGAAAGCCAGGGAGT[-/T]GGTCTGAGTGACAAG | 672 |
rs397509126 | in-del | -/TG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104163 | GGGCTACAGAAACCG[-/TG]CCAAAAGACTTCTAC | 672 |
rs397509127 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091530 | AAAGCCAGGGAGTTG[-/G]TCTGAGTGACAAGGA | 672 |
rs397509128 | in-del | -/TCTG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091526 | AAGCCAGGGAGTTGG[-/TCTG]AGTGACAAGGAATTG | 672 |
rs397509129 | in-del | -/TGA | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091497 | ATTGGTTTCAGATGA[-/TGA]AGAAAGAGGAACGGG | 672 |
rs397509130 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091488 | ATGATGAAGAAAGAG[-/G]AACGGGCTTGGAAGA | 672 |
rs397509131 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091481 | AGAAAGAGGAACGGG[-/G]CTTGGAAGAAAATAA | 672 |
rs397509132 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091479 | AAAGAGGAACGGGCT[A/T]GGAAGAAAATAATCA | 672 |
rs397509133 | in-del | -/GAAAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091470 | GGAACGGGCTTGGAA[-/GAAAA]TAATCAAGAAGAGCA | 672 |
rs397509134 | in-del | -/TAATCAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091463 | GGGCTTGGAAGAAAA[-/TAATCAA]GAAGAGCAAAGCATG | 672 |
rs397509135 | in-del | -/CAAG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091462 | TTGGAAGAAAATAAT[-/CAAG]AAGAGCAAAGCATGG | 672 |
rs397509136 | snp | A/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091459 | GAAAATAATCAAGAA[A/G/T]AGCAAAGCATGGATT | 672 |
rs397509137 | in-del | -/CT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091438 | AAGCATGGATTCAAA[-/CT]TAGGTATTGGAACCA | 672 |
rs397509138 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091437 | GCATGGATTCAAACT[-/T]AGGTATTGGAACCAG | 672 |
rs397509139 | in-del | -/ATCT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091018 | GGTGAAGCAGCATCT[-/ATCT]GGGTGTGAGAGTGAA | 672 |
rs397509140 | snp | A/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091013 | AGCAGCATCTGGGTG[A/T]GAGAGTGAAACAAGC | 672 |
rs397509141 | in-del | -/CT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090992 | GTGAAACAAGCGTCT[-/CT]GAAGACTGCTCAGGG | 672 |
rs397509142 | in-del | -/CTCTC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090967 | CTGCTCAGGGCTATC[-/CTCTC]AGAGTGACATTTTAA | 672 |
rs397509143 | in-del | -/AG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090962 | GCTATCCTCTCAGAG[-/AG]TGACATTTTAACCAC | 672 |
rs397509144 | in-del | -/TG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090961 | GCTATCCTCTCAGAG[-/TG]ACATTTTAACCACTC | 672 |
rs397509145 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090962 | GCTATCCTCTCAGAG[-/T]GACATTTTAACCACT | 672 |
rs397509146 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090957 | CCTCTCAGAGTGACA[C/T]TTTAACCACTCAGGT | 672 |
rs397509147 | in-del | -/CAG | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090944 | GACATTTTAACCACT[-/CAG]GTAAAAAGCGTGTGT | 672 |
rs397509148 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090941 | TTTAACCACTCAGGT[A/G]AAAAGCGTGTGTGTG | 672 |
rs397509149 | in-del | -/GGTA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090941 | CATTTTAACCACTCA[-/GGTA]AAAAGCGTGTGTGTG | 672 |
rs397509150 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43082576 | TTTATCGTTTTTGAA[A/G]CAGAGGGATACCATG | 672 |
rs397509151 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082560 | CAGAGGGATACCATG[C/T]AACATAACCTGATAA | 672 |
rs397509152 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082533 | ATAAAGCTCCAGCAG[G/T]AAATGGCTGAACTAG | 672 |
rs397509153 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082524 | CAGCAGGAAATGGCT[G/T]AACTAGAAGCTGTGT | 672 |
rs397509154 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082520 | AGGAAATGGCTGAAC[-/C]TAGAAGCTGTGTTAG | 672 |
rs397509155 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082518 | GAAATGGCTGAACTA[-/T]GAAGCTGTGTTAGAA | 672 |
rs397509156 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104139 | CTTCTACAGAGTGAA[C/G]CCGAAAATCCTTCCT | 672 |
rs397509157 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082508 | AACTAGAAGCTGTGT[G/T]AGAACAGCATGGGAG | 672 |
rs397509158 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082494 | TTAGAACAGCATGGG[-/G]AGCCAGCCTTCTAAC | 672 |
rs397509159 | in-del | -/AG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082478 | AGCCAGCCTTCTAAC[-/AG]CTACCCTTCCATCAT | 672 |
rs397509160 | snp | A/C | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082474 | GCCTTCTAACAGCTA[A/C]CCTTCCATCATAAGT | 672 |
rs397509161 | in-del | -/CT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082453 | CCATCATAAGTGACT[-/CT]TCTGCCCTTGAGGAC | 672 |
rs397509162 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104132 | AGAGTGAACCCGAAA[-/A]TCCTTCCTTGGTAAA | 672 |
rs397509163 | in-del | -/AT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082429 | TTGAGGACCTGCGAA[-/AT]CCAGAACAAAGCACA | 672 |
rs397509164 | in-del | -/AGAA/NNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082422 | CTGCGAAATCCAGAA[-/AGAA/NNNN]CAAAGCACATCAGAA | 672 |
rs397509165 | in-del | -/G | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43082403 | GCACATCAGAAAAAG[-/G]TGTGTATTGTTGGCC | 672 |
rs397509166 | in-del | -/AGAAAAGTAGTGAATAC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076583 | CAGTATTAACTTCAC[-/AGAAAAGTAGTGAATAC]CCTATAAGCCAGAAT | 672 |
rs397509167 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076593 | TAACTTCACAGAAAA[A/G]TAGTGAATACCCTAT | 672 |
rs397509168 | in-del | -/CCTT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104123 | AACCCGAAAATCCTT[-/CCTT]GGTAAAACCATTTGT | 672 |
rs397509169 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076580 | AAGTAGTGAATACCC[-/C]TATAAGCCAGAATCC | 672 |
rs397509170 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076576 | AGTGAATACCCTATA[-/A]GCCAGAATCCAGAAG | 672 |
rs397509171 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076573 | GAATACCCTATAAGC[C/T]AGAATCCAGAAGGCC | 672 |
rs397509172 | snp | A/G | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43104121 | GAAAATCCTTCCTTG[A/G]TAAAACCATTTGTTT | 672 |
rs397509173 | snp | A/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43104120 | AAAATCCTTCCTTGG[A/T]AAAACCATTTGTTTT | 672 |
rs397509174 | in-del | G/TT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076555 | GAATCCAGAAGGCCT[G/TT]CTGCTGACAAGTTTG | 672 |
rs397509175 | in-del | -/CAG | | | cds-indel, splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43099878 | TACCATACTGTTTAG[-/CAG]GAAACCAGTCTCAGT | 672 |
rs397509176 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076537 | GCTGACAAGTTTGAG[-/G]TGTCTGCAGATAGTT | 672 |
rs397509177 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076525 | GAGGTGTCTGCAGAT[-/A]GTTCTACCAGTAAAA | 672 |
rs397509178 | in-del | -/TACC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076517 | GTCTGCAGATAGTTC[-/TACC]AGTAAAAATAAAGAA | 672 |
rs397509179 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076516 | GCAGATAGTTCTACC[-/A]GTAAAAATAAAGAAC | 672 |
rs397509180 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076515 | CAGATAGTTCTACCA[-/G]TAAAAATAAAGAACC | 672 |
rs397509181 | in-del | -/G | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43076487 | ACCAGGAGTGGAAAG[-/G]TAAGAAACATCAATG | 672 |
rs397509182 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074478 | GATGATAGGTGGTAC[-/A]TGCACAGTTGCTCTG | 672 |
rs397509183 | in-del | -/AG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074471 | AGGTGGTACATGCAC[-/AG]TTGCTCTGGGAGTCT | 672 |
rs397509184 | in-del | -/AGAGGAGCTCA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074421 | AAACTACCCATCTCA[-/AGAGGAGCTCA]TTAAGGTTGTTGATG | 672 |
rs397509185 | in-del | -/AG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099864 | CAGGAAACCAGTCTC[-/AG]TGTCCAACTCTCTAA | 672 |
rs397509186 | in-del | -/AAACATCTTACTTGCCAAGG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074341 | CACACGATTTGACGG[-/AAACATCTTACTTGCCAAGG]CAAGATCTAGGTAAT | 672 |
rs397509187 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071233 | TTCCTTTCAGAGGGA[-/A]CCCCTTACCTGGAAT | 672 |
rs397509188 | in-del | -/CC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071229 | CTTTCAGAGGGAACC[-/CC]TTACCTGGAATCTGG | 672 |
rs397509189 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071218 | ACCCCTTACCTGGAA[-/A]TCTGGAATCAGCCTC | 672 |
rs397509190 | in-del | -/CTAACCTT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099845 | TCAGTGTCCAACTCT[-/CTAACCTT]GGAACTGTGAGAACT | 672 |
rs397509191 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071190 | TCTTCTCTGATGACC[-/C]TGAATCTGATCCTTC | 672 |
rs397509192 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099850 | AGTGTCCAACTCTCT[A/T]ACCTTGGAACTGTGA | 672 |
rs397509193 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071173 | GAATCTGATCCTTCT[G/T]AAGACAGAGCCCCAG | 672 |
rs397509194 | snp | A/C/G | 1.64977e-05 | 0.00287203 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43071171 | ATCTGATCCTTCTGA[A/C/G]GACAGAGCCCCAGAG | 672 |
rs397509195 | snp | C/G | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071154 | ACAGAGCCCCAGAGT[C/G]AGCTCGTGTTGGCAA | 672 |
rs397509196 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071150 | AGCCCCAGAGTCAGC[-/T]CGTGTTGGCAACATA | 672 |
rs397509197 | snp | A/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071137 | GCTCGTGTTGGCAAC[A/G/T]TACCATCTTCAACCT | 672 |
rs397509198 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071077 | GCAGAATCTGCCCAG[-/G]AGTCCAGCTGCTGCT | 672 |
rs397509199 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071077 | GCAGAATCTGCCCAG[-/A]GTCCAGCTGCTGCTC | 672 |
rs397509200 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071075 | AGAATCTGCCCAGAG[-/C]TCCAGCTGCTGCTCA | 672 |
rs397509201 | in-del | -/TATAATGCAATGG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071029 | ACTGATACTGCTGGG[-/TATAATGCAATGG]AAGAAAGTGTGAGCA | 672 |
rs397509202 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099834 | ACCTTGGAACTGTGA[-/G]AACTCTGAGGACAAA | 672 |
rs397509203 | in-del | -/GA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071008 | AAGTGTGAGCAGGGA[-/GA]AGCCAGAATTGACAG | 672 |
rs397509204 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071004 | TGAGCAGGGAGAAGC[-/C]AGAATTGACAGCTTC | 672 |
rs397509205 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070984 | TTGACAGCTTCAACA[G/T]AAAGGGTCAACAAAA | 672 |
rs397509206 | in-del | -/CT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099828 | GGAACTGTGAGAACT[-/CT]GAGGACAAAGCAGCG | 672 |
rs397509207 | in-del | AGA/TTTT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070967 | GAAAGGGTCAACAAA[AGA/TTTT]ATGTCCATGGTGGTG | 672 |
rs397509208 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070969 | GAAAGGGTCAACAAA[-/A]GAATGTCCATGGTGG | 672 |
rs397509209 | in-del | -/CTGGCCTGACCCCAGA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070935 | TGTCCATGGTGGTGT[-/CTGGCCTGACCCCAGA]AGAATTTGTGAGTGT | 672 |
rs397509210 | snp | C/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43070926 | CCCCAGAAGAATTTG[C/T]GAGTGTATCCATATG | 672 |
rs397509211 | snp | A/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070923 | CAGAAGAATTTGTGA[A/G/T]TGTATCCATATGTAT | 672 |
rs397509212 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43067697 | ATTTGATTTAATTTC[A/G]GATGCTCGTGTACAA | 672 |
rs397509213 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067698 | TATTTGATTTAATTT[C/G]AGATGCTCGTGTACA | 672 |
rs397509214 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067700 | AATATTTGATTTAAT[A/T]TCAGATGCTCGTGTA | 672 |
rs397509215 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067686 | TTTCAGATGCTCGTG[C/T]ACAAGTTTGCCAGAA | 672 |
rs397509216 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067685 | TTCAGATGCTCGTGT[A/G]CAAGTTTGCCAGAAA | 672 |
rs397509217 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067654 | ACACCACATCACTTT[-/T]AACTAATCTAATTAC | 672 |
rs397509218 | snp | A/C/T | 1.64961e-05 | 0.00287189 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43067624 | TGAAGAGACTACTCA[A/C/T]GTTGTTATGAAAACA | 672 |
rs397509219 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067611 | CATGTTGTTATGAAA[A/G]CAGGTATACCAAGAA | 672 |
rs397509220 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063955 | AGTGTTTTTCATTCT[A/G]CAGATGCTGAGTTTG | 672 |
rs397509221 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063959 | TTTGAGTGTTTTTCA[G/T]TCTGCAGATGCTGAG | 672 |
rs397509222 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063951 | TTTTTCATTCTGCAG[A/T]TGCTGAGTTTGTGTG | 672 |
rs397509223 | in-del | -/ATGC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063948 | TTTTTCATTCTGCAG[-/ATGC]TGAGTTTGTGTGTGA | 672 |
rs397509224 | in-del | GCTG/TTCATTCTGC | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063946 | TTTCATTCTGCAGAT[GCTG/TTCATTCTGC]AGTTTGTGTGTGAAC | 672 |
rs397509225 | in-del | -/CTG | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063946 | TTCATTCTGCAGATG[-/CTG]AGTTTGTGTGTGAAC | 672 |
rs397509226 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063939 | CAGATGCTGAGTTTG[A/T]GTGTGAACGGACACT | 672 |
rs397509227 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063928 | TTTGTGTGTGAACGG[A/G]CACTGAAATATTTTC | 672 |
rs397509228 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063914 | GACACTGAAATATTT[-/T]CTAGGAATTGCGGGA | 672 |
rs397509229 | snp | A/G/T | 3.31653e-05 | 0.00407204 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43063898 | CTAGGAATTGCGGGA[A/G/T]GAAAATGGGTAGTTA | 672 |
rs397509230 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063878 | ATGGGTAGTTAGCTA[G/T]TTCTGTAAGTATAAT | 672 |
rs397509231 | in-del | -/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43063871 | GTTAGCTATTTCTGT[-/T]AAGTATAATACTATT | 672 |
rs397509232 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063870 | TTAGCTATTTCTGTA[A/G]GTATAATACTATTTC | 672 |
rs397509233 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063364 | CTTTAGGGGTGACCC[-/A]GTCTATTAAAGAAAG | 672 |
rs397509234 | in-del | -/AAAATGCTGAATGA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063334 | TCTATTAAAGAAAGA[-/AAAATGCTGAATGA]GGTAAGTACTTGATG | 672 |
rs397509235 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063344 | ATTAAAGAAAGAAAA[-/A]TGCTGAATGAGGTAA | 672 |
rs397509236 | in-del | -/G | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43063332 | AAAATGCTGAATGAG[-/G]TAAGTACTTGATGTT | 672 |
rs397509237 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057128 | TCTTTCAGCATGATT[C/T]TGAAGTCAGAGGAGA | 672 |
rs397509238 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057126 | TTTCAGCATGATTTT[A/G]AAGTCAGAGGAGATG | 672 |
rs397509239 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057122 | AGCATGATTTTGAAG[-/T]CAGAGGAGATGTGGT | 672 |
rs397509240 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057099 | GATGTGGTCAATGGA[-/A]GAAACCACCAAGGTC | 672 |
rs397509241 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057098 | ATGTGGTCAATGGAA[-/G]AAACCACCAAGGTCC | 672 |
rs397509242 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057088 | TGGAAGAAACCACCA[A/C]GGTCCAAAGCGAGCA | 672 |
rs397509243 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057086 | GAAGAAACCACCAAG[A/G]TCCAAAGCGAGCAAG | 672 |
rs397509244 | snp | C/G | 1.64727e-05 | 0.00286986 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43057084 | AGAAACCACCAAGGT[C/G]CAAAGCGAGCAAGAG | 672 |
rs397509245 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057071 | GTCCAAAGCGAGCAA[-/A]GAGAATCCCAGGACA | 672 |
rs397509246 | snp | A/C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057071 | GTCCAAAGCGAGCAA[A/C/G]AGAATCCCAGGACAG | 672 |
rs397509247 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057063 | CGAGCAAGAGAATCC[C/T]AGGACAGAAAGGTAA | 672 |
rs397509248 | in-del | -/ACAGAAA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057053 | CAAGAGAATCCCAGG[-/ACAGAAA]GGTAAAGCTCCCTCC | 672 |
rs397509249 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057031 | GCTCCCTCCCTCAAG[G/T]TGACAAAAATCTCAC | 672 |
rs397509250 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057049 | CCAGGACAGAAAGGT[A/C]AAGCTCCCTCCCTCA | 672 |
rs397509251 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057048 | CAGGACAGAAAGGTA[A/T]AGCTCCCTCCCTCAA | 672 |
rs397509252 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057047 | AGGACAGAAAGGTAA[A/T]GCTCCCTCCCTCAAG | 672 |
rs397509253 | snp | A/T | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43051119 | TTCCTCTCTTCTTCC[A/T]GATCTTCAGGGGGCT | 672 |
rs397509254 | in-del | -/TTC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051121 | TCTCTTCCTCTCTTC[-/TTC]CAGATCTTCAGGGGG | 672 |
rs397509255 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051106 | CCAGATCTTCAGGGG[-/G]CTAGAAATCTGTTGC | 672 |
rs397509256 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051102 | ATCTTCAGGGGGCTA[G/T]AAATCTGTTGCTATG | 672 |
rs397509257 | snp | A/G | 0.000149114 | 0.00863335 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43051089 | TAGAAATCTGTTGCT[A/G]TGGGCCCTTCACCAA | 672 |
rs397509258 | snp | A/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051088 | AGAAATCTGTTGCTA[A/T]GGGCCCTTCACCAAC | 672 |
rs397509259 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051085 | AATCTGTTGCTATGG[-/G]CCCTTCACCAACATG | 672 |
rs397509260 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051084 | ATCTGTTGCTATGGG[-/G]CCCTTCACCAACATG | 672 |
rs397509261 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051080 | GTTGCTATGGGCCCT[-/T]CACCAACATGCCCAC | 672 |
rs397509262 | in-del | -/AT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051071 | GGGCCCTTCACCAAC[-/AT]GCCCACAGGTAAGAG | 672 |
rs397509263 | in-del | -/G | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43051062 | CCAACATGCCCACAG[-/G]TAAGAGCCTGGGAGA | 672 |
rs397509264 | snp | A/C/T | 1.65345e-05 | 0.00287524 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43049196 | CTAAATGTCCATTTT[A/C/T]GATCAACTGGAATGG | 672 |
rs397509265 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049197 | TCTAAATGTCCATTT[G/T]AGATCAACTGGAATG | 672 |
rs397509266 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049200 | ACATCTAAATGTCCA[G/T]TTTAGATCAACTGGA | 672 |
rs397509267 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049192 | ATGTCCATTTTAGAT[C/T]AACTGGAATGGATGG | 672 |
rs397509268 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049186 | ATTTTAGATCAACTG[G/T]AATGGATGGTACAGC | 672 |
rs397509269 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049172 | GGAATGGATGGTACA[G/T]CTGTGTGGTGCTTCT | 672 |
rs397509270 | multinucleotide-polymorphism | AG/GT | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049166 | GGATGGTACAGCTGT[AG/GT]GGTGCTTCTGTGGTG | 672 |
rs397509271 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049165 | ATGGTACAGCTGTGT[G/T]GTGCTTCTGTGGTGA | 672 |
rs397509272 | in-del | -/CTGTGGTGAAGGAGCTT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049142 | AGCTGTGTGGTGCTT[-/CTGTGGTGAAGGAGCTT]TCATCATTCACCCTT | 672 |
rs397509273 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099786 | AAAAGACGTCTGTCT[-/A]CATTGAATTGGGTAA | 672 |
rs397509274 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049150 | GGTGCTTCTGTGGTG[A/T]AGGAGCTTTCATCAT | 672 |
rs397509275 | snp | C/G/T | 1.65015e-05 | 0.00287237 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43049145 | TTCTGTGGTGAAGGA[C/G/T]CTTTCATCATTCACC | 672 |
rs397509276 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049140 | TGGTGAAGGAGCTTT[-/T]CATCATTCACCCTTG | 672 |
rs397509277 | in-del | -/GTA | | | splice-donor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43049118 | TTCACCCTTGGCACA[-/GTA]AGTATTGGGTGCCCT | 672 |
rs397509278 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049118 | CACCCTTGGCACAGT[A/T]AGTATTGGGTGCCCT | 672 |
rs397509279 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049117 | ACCCTTGGCACAGTA[A/G]GTATTGGGTGCCCTG | 672 |
rs397509280 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049114 | CTTGGCACAGTAAGT[A/G]TTGGGTGCCCTGTCA | 672 |
rs397509281 | snp | A/C | | | missense, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047696 | GGATCCAGGGTGTCC[A/C]CCCAATTGTGGTTGT | 672 |
rs397509282 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047691 | CAGGGTGTCCACCCA[-/A]TTGTGGTTGTGCAGC | 672 |
rs397509283 | snp | C/T | | | stop-gained, missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047679 | CCAATTGTGGTTGTG[C/T]AGCCAGATGCCTGGA | 672 |
rs397509284 | snp | A/G | 1.64749e-05 | 0.00287005 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43047665 | GCAGCCAGATGCCTG[A/G]ACAGAGGACAATGGC | 672 |
rs397509285 | snp | A/G | | | synonymous-codon, missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047662 | GCCAGATGCCTGGAC[A/G]GAGGACAATGGCTTC | 672 |
rs397509286 | in-del | -/AG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047659 | CAGATGCCTGGACAG[-/AG]GACAATGGCTTCCAT | 672 |
rs397509287 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047638 | TGGCTTCCATGGTAA[C/G]GTGCCTGCATGTACC | 672 |
rs397509288 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045787 | CAATTGGGCAGATGT[-/G]TGAGGCACCTGTGGT | 672 |
rs397509289 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43097289 | GGGGAAATTTTTTAG[-/G]ATCTGATTCTTCTGA | 672 |
rs397509290 | in-del | -/GTGACCCGAG | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045764 | TGTGAGGCACCTGTG[-/GTGACCCGAG]AGTGGGTGTTGGACA | 672 |
rs397509291 | in-del | -/C | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045767 | GCACCTGTGGTGACC[-/C]GAGAGTGGGTGTTGG | 672 |
rs397509292 | in-del | -/G | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045758 | GTGACCCGAGAGTGG[-/G]TGTTGGACAGTGTAG | 672 |
rs397509293 | in-del | -/G | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045737 | GACAGTGTAGCACTC[-/G]TACCAGTGCCAGGAG | 672 |
rs397509294 | in-del | -/T | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045736 | ACAGTGTAGCACTCT[-/T]ACCAGTGCCAGGAGC | 672 |
rs397509295 | snp | A/C/G | 1.65007e-05 | 0.00287229 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43045729 | AGCACTCTACCAGTG[A/C/G]CAGGAGCTGGACACC | 672 |
rs397509296 | in-del | -/C | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045722 | TACCAGTGCCAGGAG[-/C]TGGACACCTACCTGA | 672 |
rs397509297 | in-del | -/C | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045716 | TGCCAGGAGCTGGAC[-/C]ACCTACCTGATACCC | 672 |
rs397509298 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43097281 | TTTTTAGGATCTGAT[G/T]CTTCTGAAGATACCG | 672 |
rs397509299 | snp | C/T | | | stop-gained, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124042 | GTCATTAATGCTATG[C/T]AGAAAATCTTAGAGT | 672 |
rs397509300 | in-del | -/AACG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43097267 | TTCTTCTGAAGATAC[-/AACG]CGTTAATAAGGCAAC | 672 |
rs397509301 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095900 | GATCAAGAATTGTTA[C/T]AAATCACCCCTCAAG | 672 |
rs397509302 | in-del | -/AGGGATGAAATCAGGAGCCA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095891 | TTGTTACAAATCACC[-/AGGGATGAAATCAGGAGCCA]CCTCAAGGAACCAGG | 672 |
rs397509303 | in-del | -/T | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124034 | TGCTATGCAGAAAAT[-/T]CTTAGAGTGTCCCAT | 672 |
rs397509304 | in-del | -/TT | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124032 | GCTATGCAGAAAATC[-/TT]AGAGTGTCCCATCTG | 672 |
rs397509305 | in-del | -/AA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095848 | TTGGATTCTGCAAAA[-/AA]GGGTAATGGCAAAGT | 672 |
rs397509306 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095848 | TGGATTCTGCAAAAA[A/G]GGGTAATGGCAAAGT | 672 |
rs397509307 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094853 | ATTTTCAGCTGCTTG[-/C]TGAATTTTCTGAGAC | 672 |
rs397509308 | snp | A/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094853 | ATTTTCAGCTGCTTG[A/T]GAATTTTCTGAGACG | 672 |
rs397509309 | in-del | -/A | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124028 | GCAGAAAATCTTAGA[-/A]GTGTCCCATCTGGTA | 672 |
rs397509310 | in-del | -/TGTC | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124023 | AAATCTTAGAGTGTC[-/TGTC]CCATCTGGTAAGTCA | 672 |
rs397509311 | in-del | -/TC | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124024 | GAAAATCTTAGAGTG[-/TC]CCATCTGGTAAGTCA | 672 |
rs397509312 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094794 | CCAGTAATAATGATT[-/T]GAACACCACTGAGAA | 672 |
rs397509313 | snp | A/C | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124024 | AAAATCTTAGAGTGT[A/C]CCATCTGGTAAGTCA | 672 |
rs397509314 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094788 | ATAATGATTTGAACA[-/A]CCACTGAGAAGCGTG | 672 |
rs397509315 | in-del | -/CATCTG | | | splice-donor-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124016 | AGAGTGTCCCATCTG[-/CATCTG]GTAAGTCAGCACAAG | 672 |
rs397509316 | in-del | -/A/AG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094762 | CGTGCAGCTGAGAGG[-/A/AG]CATCCAGAAAAGTAT | 672 |
rs397509317 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094745 | TCCAGAAAAGTATCA[A/G]GGTAGTTCTGTTTCA | 672 |
rs397509318 | snp | A/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094744 | CCAGAAAAGTATCAG[A/G/T]GTAGTTCTGTTTCAA | 672 |
rs397509319 | snp | A/C/G/T | | | missense, splice-donor-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094743 | CAGAAAAGTATCAGG[A/C/G/T]TAGTTCTGTTTCAAA | 672 |
rs397509320 | snp | C/T | | | synonymous-codon, splice-donor-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094742 | AGAAAAGTATCAGGG[C/T]AGTTCTGTTTCAAAC | 672 |
rs397509321 | snp | A/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094741 | GAAAAGTATCAGGGT[A/G/T]GTTCTGTTTCAAACT | 672 |
rs397509322 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094740 | AAAAGTATCAGGGTA[A/G]TTCTGTTTCAAACTT | 672 |
rs397509323 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094731 | AGGGTAGTTCTGTTT[-/T]CAAACTTGCATGTGG | 672 |
rs397509324 | in-del | -/T | | | splice-donor-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124014 | AGTGTCCCATCTGGT[-/T]AAGTCAGCACAAGAG | 672 |
rs397509325 | in-del | -/TCAG | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124008 | GTCCCATCTGGTAAG[-/TCAG]CACAAGAGTGTATTA | 672 |
rs397509326 | snp | A/C/G | | | splice-acceptor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43115781 | CCCCCCTACCCTGCT[A/C/G]GTCTGGAGTTGATCA | 672 |
rs397509327 | snp | A/G | 0.000198252 | 0.00995423 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094707 | ATGTGGAGCCATGTG[A/G]CACAAATACTCATGC | 672 |
rs397509328 | snp | C/T | 0.000115587 | 0.00760132 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094706 | TGTGGAGCCATGTGG[C/T]ACAAATACTCATGCC | 672 |
rs397509329 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094703 | GGAGCCATGTGGCAC[-/T]AAATACTCATGCCAG | 672 |
rs397509330 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094681 | CATGCCAGCTCATTA[C/T]AGCATGAGAACAGCA | 672 |
rs397509331 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115771 | CTGCTAGTCTGGAGT[A/T]GATCAAGGAACCTGT | 672 |
rs397509332 | snp | C/G/T | 1.66407e-05 | 0.00288446 | BRCA1, NBR2 | 17 | allele_origin=G(germline)/T(germline) | 17:43124089 | AGAAAGAAATGGATT[C/G/T]ATCTGCTCTTCGCGT | 672 |
rs397509333 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094627 | ATGAATGTAGAAAAG[-/C]GCTGAATTCTGTAAT | 672 |
rs397509334 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094622 | TGTAGAAAAGGCTGA[-/A]TTCTGTAATAAAAGC | 672 |
rs397509335 | in-del | AGC/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094607 | GAATTCTGTAATAAA[AGC/T]AAACAGCCTGGCTTA | 672 |
rs397509336 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094607 | ATTCTGTAATAAAAG[-/C]AAACAGCCTGGCTTA | 672 |
rs397509337 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094604 | CTGTAATAAAAGCAA[-/A]CAGCCTGGCTTAGCA | 672 |
rs397509338 | snp | C/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094603 | TGTAATAAAAGCAAA[C/T]AGCCTGGCTTAGCAA | 672 |
rs397509339 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094571 | GGAGCCAACATAACA[-/GA]TGGGCTGGAAGTAAG | 672 |
rs397509340 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094570 | AGCCAACATAACAGA[-/T]GGGCTGGAAGTAAGG | 672 |
rs397509341 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094545 | AGTAAGGAAACATGT[-/AA]TGATAGGCGGACTCC | 672 |
rs397763555 | in-del | -/CCT | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095108 | GCAGAAACCACACCT[-/CCT]ATTTCTCTAACGTCT | 672 |
rs397857709 | in-del | -/T | 0.399819 | 0.200136 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044805 | CTAGTTTCATTTTCC[-/T]TTTTTTTTTTTTTTT | 672 |
rs397952054 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077763 | TTTGAGATGGAGTTT[-/T]GCTCTTGTTGCCCAG | 672 |
rs397952458 | in-del | -/CAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059515 | CAACAACAACAACAA[-/CAA]ATTCTCACATCTAAA | 672 |
rs397960145 | in-del | -/GGAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075086 | GAAGGAAGGAAGGAA[-/GGAA]AGGAAGAAAGAAAGG | 672 |
rs397967320 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044823 | TTTTTTTTTTTTTTT[-/T]GAGCCACAGTCTCAC | 672 |
rs398030894 | in-del | -/A | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054760 | GGGAGACTTCATCTC[-/A]AAAAAAAAAAAAAAA | 672 |
rs398030897 | in-del | -/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115516 | TTGACATATATTATC[-/T]TTTTTTTTTTTTTTG | 672 |
rs398030898 | in-del | -/T | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119288 | CTTGTGATCCTTTTC[-/T]TTTTTTTTTTTCTTT | 672 |
rs398041704 | in-del | -/T | 0.5 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098046 | TTTTTTTTTTTTTTT[-/T]GGAGGTCTTGCTCTG | 672 |
rs398119829 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123073 | AAAAAGAAAAAAAAA[-/A]TACAAAAATTAGCTG | 672 |
rs398122352 | in-del | -/AAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090937 | TAACCACTCAGGTAA[-/AAA]GCGTGTGTGTGTGTG | 672 |
rs398122353 | in-del | -/T | 1.65751e-05 | 0.00287876 | BRCA1 | 17 | allele_origin=T(germline)/+.-----(germline) | 17:43097292 | TGGGGGGAAATTTTT[-/T]AGGATCTGATTCTTC | 672 |
rs398122354 | in-del | -/ATT | 3.13957e-05 | 0.00396193 | BRCA1 | 17 | allele_origin=A(germline)/+.-----(germline) | 17:43094876 | TTTGAGTACCTTGTT[-/ATT]TTTGTATATTTTCAG | 672 |
rs398122626 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124123 | TATGTTTTTCTAATG[C/T]GTTAAAGTTCATTGG | 672 |
rs398122627 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094438 | TGCTCAGAGAATCCT[A/T]GAGATACTGAAGATG | 672 |
rs398122628 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094275 | ACGTTCTAAATGAGG[G/T]AGATGAATATTCTGG | 672 |
rs398122629 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094239 | CAGAGAAAATAGACT[-/T]ACTGGCCAGTGATCC | 672 |
rs398122630 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094204 | GAGGCTTTAATATGT[A/T]AAAGTGAAAGAGTTC | 672 |
rs398122631 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094194 | TATGTAAAAGTGAAA[-/A]GAGTTCACTCCAAAT | 672 |
rs398122632 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094170 | CCAAATCAGTAGAGA[-/G]TAATATTGAAGACAA | 672 |
rs398122633 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094153 | TAATATTGAAGACAA[-/AA]TATTTGGGAAAACCT | 672 |
rs398122634 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094152 | ATATTGAAGACAAAA[G/T]ATTTGGGAAAACCTA | 672 |
rs398122635 | snp | A/C/T | 1.74327e-05 | 0.00295229 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43106527 | AATTTATAGATTTTG[A/C/T]ATGCTGAAACTTCTC | 672 |
rs398122636 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094018 | AATAAATTAAAGCGT[-/T]AAAAGGAGACCTACA | 672 |
rs398122637 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094008 | AGCGTAAAAGGAGAC[C/T]TACATCAGGCCTTCA | 672 |
rs398122638 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093924 | TGATAAATCAGGGAA[C/G]TAACCAAACGGAGCA | 672 |
rs398122639 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093922 | ATAAATCAGGGAACT[A/G]ACCAAACGGAGCAGA | 672 |
rs398122640 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093903 | AAACGGAGCAGAATG[-/G]TCAAGTGATGAATAT | 672 |
rs398122641 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093787 | GAATCTGCTTTCAAA[-/A]CGAAAGCTGAACCTA | 672 |
rs398122642 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093772 | ACGAAAGCTGAACCT[-/A]TAAGCAGCAGTATAA | 672 |
rs398122643 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093732 | AACTCGAATTAAATA[G/T]CCACAATTCAAAAGC | 672 |
rs398122644 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093703 | GCACCTAAAAAGAAT[A/G]GGCTGAGGAGGAAGT | 672 |
rs398122645 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093687 | GGCTGAGGAGGAAGT[C/T]TTCTACCAGGCATAT | 672 |
rs398122646 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093656 | TCATGCGCTTGAACT[-/A]GTAGTCAGTAGAAAT | 672 |
rs398122647 | snp | C/T | 1.64876e-05 | 0.00287116 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093633 | GTAGAAATCTAAGCC[C/T]ACCTAATTGTACTGA | 672 |
rs398122648 | in-del | -/G | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124078 | GATTTATCTGCTCTT[-/G]CGCGTTGAAGAAGTA | 672 |
rs398122649 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093624 | TAAGCCCACCTAATT[A/G]TACTGAATTGCAAAT | 672 |
rs398122650 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093610 | TGTACTGAATTGCAA[-/A]TTGATAGTTGTTCTA | 672 |
rs398122651 | in-del | -/TA | | | frameshift-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43106464 | TATGTAAGAATGATA[-/TA]ACCAAAAGGTATATA | 672 |
rs398122652 | snp | A/C/T | 1.74136e-05 | 0.00295067 | BRCA1 | 17 | allele_origin=T(germline)/A(germline)/C(germline) | 17:43106452 | TATAACCAAAAGGTA[A/C/T]ATAATTTGGTAATGA | 672 |
rs398122653 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093399 | CCTGGTTCTTTTACT[-/AA]GTGTTCAAATACCAG | 672 |
rs398122654 | in-del | -/GA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093284 | TGAAGACCCCAAAGA[-/GA]TCTCATGTTAAGTGG | 672 |
rs398122655 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093235 | GAAAGATCTGTAGAG[A/G]GTAGCAGTATTTCAT | 672 |
rs398122656 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093229 | TCTGTAGAGAGTAGC[A/G]GTATTTCATTGGTAC | 672 |
rs398122657 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093144 | TAGGGAAGGCAAAAA[-/A]CAGAACCAAATAAAT | 672 |
rs398122658 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093139 | AAGGCAAAAACAGAA[C/T]CAAATAAATGTGTGA | 672 |
rs398122659 | in-del | -/CAACTTGTTGA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104918 | AGTACGAGATTTAGT[-/CAACTTGTTGA]AGAGCTATTGAAAAT | 672 |
rs398122660 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093108 | GTCAGTGTGCAGCAT[C/T]TGAAAACCCCAAGGG | 672 |
rs398122661 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104919 | TTTAGTCAACTTGTT[G/T]AAGAGCTATTGAAAA | 672 |
rs398122662 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092980 | GAAATGGAAGAAAGT[A/G]AACTTGATGCTCAGT | 672 |
rs398122663 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092877 | AGGAATGTGCAACAT[-/T]CTCTGCCCACTCTGG | 672 |
rs398122664 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092844 | CCTTAAAGAAACAAA[-/A]GTCCAAAAGTCACTT | 672 |
rs398122665 | snp | A/C/G | | | missense, synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092825 | AAAAGTCACTTTTGA[A/C/G]TGTGAACAAAAGGAA | 672 |
rs398122666 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092785 | GGAAAGAATGAGTCT[A/T]ATATCAAGCCTGTAC | 672 |
rs398122667 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092783 | AAAGAATGAGTCTAA[-/T]ATCAAGCCTGTACAG | 672 |
rs398122668 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092777 | TGAGTCTAATATCAA[G/T]CCTGTACAGACAGTT | 672 |
rs398122669 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092757 | TACAGACAGTTAATA[-/T]CACTGCAGGCTTTCC | 672 |
rs398122670 | in-del | -/TC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092628 | CTGGACTCATTACTC[-/TC]CAAATAAACATGGAC | 672 |
rs398122671 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092380 | GAAGTAGGTTCCAGT[A/G]CTAATGAAGTGGGCT | 672 |
rs398122672 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092376 | TAGGTTCCAGTACTA[A/G]TGAAGTGGGCTCCAG | 672 |
rs398122673 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092327 | CAGTGATGAAAACAT[-/T]CAAGCAGAACTAGGT | 672 |
rs398122674 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091931 | ATACACATTTGGCTC[-/AG]GGTTACCGAAGAGGG | 672 |
rs398122675 | snp | A/G/T | 4.94874e-05 | 0.00497406 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43091889 | AGAGTCCTCAGAAGA[A/G/T]AACTTATCTAGTGAG | 672 |
rs398122676 | snp | C/G | 3.29761e-05 | 0.00406041 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43091881 | CAGAAGAGAACTTAT[C/G]TAGTGAGGATGAAGA | 672 |
rs398122677 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091859 | GGATGAAGAGCTTCC[-/C]TGCTTCCAACACTTG | 672 |
rs398122678 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091634 | CTTGTTTTCTTCACA[G/T]TGCAGTGAATTGGAA | 672 |
rs398122679 | in-del | -/TAAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091466 | GGGCTTGGAAGAAAA[-/TAAT]CAAGAAGAGCAAAGC | 672 |
rs398122680 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091443 | AGCAAAGCATGGATT[C/T]AAACTTAGGTATTGG | 672 |
rs398122681 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091437 | GCATGGATTCAAACT[G/T]AGGTATTGGAACCAG | 672 |
rs398122682 | in-del | -/TT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091012 | GCAGCATCTGGGTGT[-/TT]GAGAGTGAAACAAGC | 672 |
rs398122683 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082578 | CATTTATCGTTTTTG[A/G]AGCAGAGGGATACCA | 672 |
rs398122684 | snp | A/C/G | 1.64743e-05 | 0.00287 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43082489 | ACAGCATGGGAGCCA[A/C/G]CCTTCTAACAGCTAC | 672 |
rs398122685 | snp | A/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082407 | CAAAGCACATCAGAA[A/T]AAGGTGTGTATTGTT | 672 |
rs398122686 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076555 | AATCCAGAAGGCCTT[C/T]CTGCTGACAAGTTTG | 672 |
rs398122687 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074513 | TTTCTAGGTCATCCC[-/C]TTCTAAATGCCCATC | 672 |
rs398122688 | snp | A/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074462 | TGCACAGTTGCTCTG[A/G/T]GAGTCTTCAGAATAG | 672 |
rs398122689 | snp | A/C/T | 1.64754e-05 | 0.00287009 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43074417 | AAGAGGAGCTCATTA[A/C/T]GGTTGTTGATGTGGA | 672 |
rs398122690 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063954 | GTGTTTTTCATTCTG[C/G]AGATGCTGAGTTTGT | 672 |
rs398122691 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063897 | TAGGAATTGCGGGAG[A/G]AAAATGGGTAGTTAG | 672 |
rs398122692 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063340 | AAGAAAGAAAAATGC[-/T]GAATGAGGTAAGTAC | 672 |
rs398122693 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057132 | GGTTTCTTTCAGCAT[A/G]ATTTTGAAGTCAGAG | 672 |
rs398122694 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051110 | TCTTCCAGATCTTCA[G/T]GGGGCTAGAAATCTG | 672 |
rs398122695 | snp | C/T | 1.65674e-05 | 0.00287809 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43051068 | CCTTCACCAACATGC[C/T]CACAGGTAAGAGCCT | 672 |
rs398122696 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051065 | TCACCAACATGCCCA[C/T]AGGTAAGAGCCTGGG | 672 |
rs398122697 | snp | C/T | 1.64993e-05 | 0.00287218 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43049170 | AATGGATGGTACAGC[C/T]GTGTGGTGCTTCTGT | 672 |
rs398122698 | snp | A/G | | | missense, stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047652 | TGGACAGAGGACAAT[A/G]GCTTCCATGGTAAGG | 672 |
rs398122699 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43045804 | GTGTTCTCTGTCTCC[A/G]GCAATTGGGCAGATG | 672 |
rs398122700 | snp | A/G | | | missense, stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045797 | CTGTCTCCAGCAATT[A/G]GGCAGATGTGTGAGG | 672 |
rs398122701 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097307 | TATTGATTTATTTTT[-/T]GGGGGGAAATTTTTT | 672 |
rs398122702 | snp | C/T | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045754 | CCCGAGAGTGGGTGT[C/T]GGACAGTGTAGCACT | 672 |
rs398122703 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095909 | AGTGTGGGAGATCAA[A/G]AATTGTTACAAATCA | 672 |
rs398122704 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095870 | GGAACCAGGGATGAA[A/G]TCAGTTTGGATTCTG | 672 |
rs398122705 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095851 | GTTTGGATTCTGCAA[A/G]AAAGGGTAATGGCAA | 672 |
rs398122706 | snp | G/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43095845 | ATTCTGCAAAAAAGG[G/T]TAATGGCAAAGTTTG | 672 |
rs398122707 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43094870 | CCTTGTTATTTTTGT[A/G]TATTTTCAGCTGCTT | 672 |
rs398122708 | snp | A/G/T | 1.97031e-05 | 0.00313865 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43094836 | AATTTTCTGAGACGG[A/G/T]TGTAACAAATACTGA | 672 |
rs398122709 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094595 | AAGCAAACAGCCTGG[-/C]TTAGCAAGGAGCCAA | 672 |
rs431825382 | in-del | -/CTGT | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045573 | TCTTCAGTCCTTCTA[-/CTGT]CCTGGCTACTAAATA | 672 |
rs431825383 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124109 | GTGTTAAAGTTCATT[A/G]GAACAGAAAGAAATG | 672 |
rs431825384 | in-del | -/AT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094382 | GCATTCAGAAAGTTA[-/AT]GAGTGGTTTTCCAGA | 672 |
rs431825385 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115729 | GTGACCACATATTTT[-/T]GCAAGTAAGTTTGAA | 672 |
rs431825386 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094097 | CTTAAGCCATGTAAC[-/T]GAAAATCTAATTATA | 672 |
rs431825387 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093951 | GATTTGGCAGTTCAA[-/AA]GACTCCTGAAATGAT | 672 |
rs431825388 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093450 | GTAAAAGACATGACA[A/G]CGATACTTTCCCAGA | 672 |
rs431825389 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093429 | ACTTTCCCAGAGCTG[-/AA]GTTAACAAATGCACC | 672 |
rs431825390 | in-del | -/TG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093198 | CTGGTACTGATTATG[-/TG]GCACTCAGGAAAGTA | 672 |
rs431825391 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092883 | CAGAAGAGGAATGTG[C/T]AACATTCTCTGCCCA | 672 |
rs431825392 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092799 | AGGAAGAAAATCAAG[A/G]AAAGAATGAGTCTAA | 672 |
rs431825393 | snp | C/G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104879 | CTTTTCAGCTTGACA[C/G/T]AGGTTTGGAGTGTAA | 672 |
rs431825394 | snp | A/C/G | 1.64977e-05 | 0.00287203 | BRCA1 | 17 | allele_origin=G(germline)/A(germline)/C(germline) | 17:43092621 | CATTACTCCAAATAA[A/C/G]CATGGACTTTTACAA | 672 |
rs431825395 | snp | A/C/T | 1.65015e-05 | 0.00287237 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43092125 | GATAACTTAGAACAG[A/C/T]CTATGGGAAGTAGTC | 672 |
rs431825396 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092098 | AGTCATGCATCTCAG[G/T]TTTGTTCTGAGACAC | 672 |
rs431825397 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104195 | TAAAAGATGAAGTTT[-/C]TATCATCCAAAGTAT | 672 |
rs431825398 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091772 | TACCGAGTGTCTGTC[-/T]AAGAACACAGAGGAG | 672 |
rs431825399 | snp | A/G/T | 1.64749e-05 | 0.00287005 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43091757 | TAAGAACACAGAGGA[A/G/T]AATTTATTATCATTG | 672 |
rs431825400 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091713 | ATGACTGCAGTAACC[A/G]GGTAATATTGGCAAA | 672 |
rs431825401 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091662 | TTAGTGAGGAAACAA[A/C]ATGTTCTGCTAGCTT | 672 |
rs431825402 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091617 | GCAGTGAATTGGAAG[A/T]CTTGACTGCAAATAC | 672 |
rs431825403 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091576 | GATCCTTTCTTGATT[A/G]GTTCTTCCAAACAAA | 672 |
rs431825404 | in-del | -/AAGA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091490 | TTCAGATGATGAAGA[-/AAGA]GGAACGGGCTTGGAA | 672 |
rs431825405 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091435 | ATGGATTCAAACTTA[A/G]GTATTGGAACCAGGT | 672 |
rs431825406 | snp | A/T | | | splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43090942 | TTTTAACCACTCAGG[A/T]AAAAAGCGTGTGTGT | 672 |
rs431825407 | snp | A/G | 1.65012e-05 | 0.00287234 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43082397 | CAGAAAAAGGTGTGT[A/G]TTGTTGGCCAAACAC | 672 |
rs431825408 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076589 | TTCACAGAAAAGTAG[A/T]GAATACCCTATAAGC | 672 |
rs431825409 | in-del | -/TAAG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074416 | TCAAGAGGAGCTCAT[-/TAAG]GTTGTTGATGTGGAG | 672 |
rs431825410 | in-del | -/TTAAC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067652 | AAACACCACATCACT[-/TTAAC]TAATCTAATTACTGA | 672 |
rs431825411 | snp | A/G/T | 3.30574e-05 | 0.00406544 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43067603 | TATGAAAACAGGTAT[A/G/T]CCAAGAACCTTTACA | 672 |
rs431825412 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057124 | TCAGCATGATTTTGA[A/T]GTCAGAGGAGATGTG | 672 |
rs431825413 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057064 | GCGAGCAAGAGAATC[-/C]CCAGGACAGAAAGGT | 672 |
rs431825414 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057060 | GCAAGAGAATCCCAG[-/C]GACAGAAAGGTAAAG | 672 |
rs431825415 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057053 | AATCCCAGGACAGAA[A/G]GGTAAAGCTCCCTCC | 672 |
rs431825416 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051093 | GGGCTAGAAATCTGT[G/T]GCTATGGGCCCTTCA | 672 |
rs431825417 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047640 | AATGGCTTCCATGGT[A/C]AGGTGCCTGCATGTA | 672 |
rs431825418 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095857 | AAATCAGTTTGGATT[C/G]TGCAAAAAAGGGTAA | 672 |
rs431825419 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095846 | GATTCTGCAAAAAAG[A/G]GTAATGGCAAAGTTT | 672 |
rs431825420 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094533 | GTAATGATAGGCGGA[C/T]TCCCAGCACAGAAAA | 672 |
rs483353071 | in-del | GTGGTTT/NNNNNNNNNNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057091 | TCGCTTTGGACCTTG[GTGGTTT/NNNNNNNNNNNN]CTTCCATTGACCACA | 672 |
rs483353078 | in-del | -/NNNNNNNNNNNNNNNNN | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093026 | CTGTGGTTAACTTCA[-/NNNNNNNNNNNNNNNNN]TGTCCCAATGGATAC | 672 |
rs483353079 | in-del | -/NNNNNNNNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090973 | GTCACTCTGAGAGGA[-/NNNNNNNNNN]TAGCCCTGAGCAGTC | 672 |
rs483353083 | in-del | -/NNNN | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094232 | TCATGAGGATCACTG[-/NNNN]GCCAGTAAGTCTATT | 672 |
rs483353084 | in-del | -/NNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076521 | TATTTTTACTGGTAG[-/NNNN]AACTATCTGCAGACA | 672 |
rs483353085 | in-del | ATAGAATCACCTTTTGTTTTATTCTCATGACCACTATTAGTAATATTCA/NNNNN | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093846 | TTTTTCTCATTCTGA[lengthTooLong]TCACTTGACCATTCT | 672 |
rs483353086 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093432 | CATTTGTTAACTTCA[-/T]GCTCTGGGAAAGTAT | 672 |
rs483353087 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093175 | GAGTGCTAACTTCCA[A/G]TAACGAGATACTTTC | 672 |
rs483353088 | in-del | -/NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092242 | ACTTCCAGGAAGACT[lengthTooLong]TTGTTTATAGACCTC | 672 |
rs483353089 | in-del | -/NNNN | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091959 | TATGGGTGAAAGGGC[-/NNNN]TAGGACTCCTGCTAA | 672 |
rs483353090 | snp | G/T | 3.29495e-05 | 0.00405877 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43091755 | TTCAATGATAATAAA[G/T]TCTCCTCTGTGTTCT | 672 |
rs483353091 | in-del | CTGTG/NNNNNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104877 | ACTTACACTCCAAAC[CTGTG/NNNNNNN]TCAAGCTGAAAAGCA | 672 |
rs483353092 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091480 | ATTATTTTCTTCCAA[-/C]GCCCGTTCCTCTTTC | 672 |
rs483353093 | in-del | -/CT | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43104262 | TATAGCTGTTTGCAT[-/CT]GTAAAATACAAGGGA | 672 |
rs483353094 | in-del | -/NNNNNNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074361 | CAAGTAAGATGTTTC[-/NNNNNNNN]CGTCAAATCGTGTGG | 672 |
rs483353095 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071217 | AGAGGCTGATTCCAG[-/T]ATTCCAGGTAAGGGG | 672 |
rs483353096 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071088 | GGACTCTGGGCAGAT[C/T]CTGCAACTTTCAATT | 672 |
rs483353097 | in-del | -/NNNNNNNNNNNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067674 | GATGTGGTGTTTTCT[-/NNNNNNNNNNNNN]GGCAAACTTGTACAC | 672 |
rs483353098 | in-del | -/NNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067648 | TCTTCAGTAATTAGA[-/NNNN]TTAGTTAAAGTGATG | 672 |
rs483353099 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063928 | GAAAATATTTCAGTG[-/T]CCGTTCACACACAAA | 672 |
rs483353100 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063362 | TTCTTTCTTTAATAG[A/G]CTGGGTCACCCCTAA | 672 |
rs483353101 | in-del | -/NNNNNNNNNNNNNNNNNNNN | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057004 | AGGGGAGTGGAATAC[-/NNNNNNNNNNNNNNNNNNNN]AGAGTGGTGGGGTGA | 672 |
rs483353102 | in-del | ACTGGT/NNNNNNNNNNNNNNNNNNNN | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045731 | TGTCCAGCTCCTGGC[ACTGGT/NNNNNNNNNNNNNNNNNNNN]AGAGTGCTACACTGT | 672 |
rs483353103 | in-del | NNNNNN/T | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045707 | GGGGGATCTGGGGTA[NNNNNN/T]CAGGTAGGTGTCCAG | 672 |
rs483353104 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099858 | CCAAGGTTAGAGAGT[-/T]GGACACTGAGACTGG | 672 |
rs483353105 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099852 | ACAGTTCCAAGGTTA[-/G]AGAGTTGGACACTGA | 672 |
rs483353106 | in-del | -/NNNNNNNNNNNNNNNNNNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095890 | CCCTGGTTCCTTGAG[-/NNNNNNNNNNNNNNNNNNNN]GGGTGATTTGTAACA | 672 |
rs483353107 | in-del | -/NNNNNNNNNNN | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094723 | ACATGGCTCCACATG[-/NNNNNNNNNNN]CAAGTTTGAAACAGA | 672 |
rs483353108 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094697 | AATGAGCTGGCATGA[-/T]GTATTTGTGCCACAT | 672 |
rs483353109 | in-del | -/NNNNNNN | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094679 | CTGCTGTTCTCATGC[-/NNNNNNN]TGTAATGAGCTGGCA | 672 |
rs527251997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111637 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTTTCT | 672 |
rs527283522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054679 | CTCCTGGGCTCAAGT[A/G]ATCCTCCTGCCTTGG | 672 |
rs527323270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110978 | TGGTGGTGCACGCCT[A/G]TAATCCCAGCTACTT | 672 |
rs527352287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049067 | CAGGTGCCAGTCTTG[C/T]TCACAGGAGAGAATA | 672 |
rs527390046 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119136 | CTGGCAGTGTGACAA[G/T]AATGTGGTTTTTTCC | 672 |
rs527394918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103597 | AAGTAGCTGGGATTA[C/T]AGGTACATTCACCTC | 672 |
rs527414650 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055791 | ACAAAAAATTAGCTA[A/G]TTGTTGTGGCACATG | 672 |
rs527441265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117796 | TCACCCAAGTTCCCA[G/T]CCCTACCTGTCTATC | 672 |
rs527449526 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125357 | TCCCCCGTCCAGGAA[A/G]TCTCAGCGAGCTCAC | 672 |
rs527460495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078008 | CCAAAGTGATGGGAT[C/T]ACAGGCGTGAGCCAC | 672 |
rs527537657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062225 | TAGCTTCCTCAGTAG[C/T]TAAGACTACAGAAGC | 672 |
rs527555690 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109158 | GCCATTGCGCTGGGC[G/T]ACTTTCTATCTTTAT | 672 |
rs527589832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118318 | CAGAGAGGTAGCTGG[C/T]AACTTCTGGTAGGAA | 672 |
rs527601907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061652 | CAGTGGTGCAATCTA[A/G]GCTCACTGCAACCTC | 672 |
rs527652099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119838 | TATTTCAGTATGGTA[A/G]TTATAATCTAAACTA | 672 |
rs527674943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071446 | TTAACACGTATTTAC[A/G]CTTTCAGTCAACAAT | 672 |
rs527725740 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045193 | TGCCCAAGGACTATT[C/T]TGACTTTAAGTCACA | 672 |
rs527763939 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120547 | GAGGTGGGCGGATCA[C/T]GAGGTCAGGAAGTGG | 672 |
rs527763960 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048322 | ATTCTCCTGCCCCAG[C/G]CCCTCAAGTAGCTGG | 672 |
rs527865313 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088366 | CCATCCTATGAATTT[A/G]TCTTTTTTTTTTTTT | 672 |
rs527906133 | in-del | -/TTTC | 0.0193772 | 0.0965046 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083162 | GAACCTTTAGTTTCT[-/TTTC]TTTCTTTCTTTCTTT | 672 |
rs527936361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070809 | ATTAAATTACACAGA[A/C]CTGTGATTGTTTTCT | 672 |
rs527945380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079491 | GGCAAAACTGGAAAA[A/G]TCTACAACGTGACCC | 672 |
rs527981911 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125931 | ATTCTCACGGAAATC[C/T]AGTGGATAGATTGGA | 672 |
rs528049263 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044408 | GGGGGCTAGGGAAGA[A/C]CTAGTCCTTCCAACA | 672 |
rs528055173 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123506 | AGGCACATGCCACTA[C/G]GCCCAGCTAATTTTT | 672 |
rs528116803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083904 | GTCTTGCTCTGTTGC[C/T]CCAGGCTGGAGTGCA | 672 |
rs528123140 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117854 | GTTCATTTATTATAC[A/T]AATATAACAAGTGTT | 672 |
rs528143045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060158 | TCACCACAACCTCCA[C/T]CTCCCGGGTTGATGA | 672 |
rs528161690 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080607 | TCCAGGAGTTTGAGA[C/T]CAACTTGGGCAACAT | 672 |
rs528170710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123988 | TAATCATAGGAATCC[A/C]AAATTAATACACTCT | 672 |
rs528175816 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120802 | AATCTTAAGCCAGGC[A/G]CAGTGGCTCACGCCA | 672 |
rs528189318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067327 | TGGCATGATCTCGGC[C/T]CACTGCAACCTCCAT | 672 |
rs528231620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054846 | CTCCTGGGTTCAACC[A/G]ATTCTCTAGCCTCAG | 672 |
rs528254652 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092318 | TCTGTTTCTACCTAG[C/T]TCTGCTTGAATGTTT | 672 |
rs528367516 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058381 | TCTGCTAAAAAAAAA[A/C]ACACACACACACACA | 672 |
rs528383360 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054678 | ACTCCTGGGCTCAAG[C/T]GATCCTCCTGCCTTG | 672 |
rs528390541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082703 | TGGAACTACAAGTTC[A/T]AGCTGAACACCTTTT | 672 |
rs528651512 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109114 | ATCGCCTGCTTCAGC[C/T]TCCCAAAGTGCTGGG | 672 |
rs528681099 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052542 | GGCATAGGTTCTTAG[C/G/T]AAATAACTTGGGTAT | 672 |
rs528715943 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095607 | AAACAAACAAACAAA[A/C]AAAAAAACGAAAGGG | 672 |
rs528716582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117057 | GTACTGTGTACTCTT[A/G]TTAGATCACTTCAGA | 672 |
rs528807218 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110274 | AATGAACTTGTATAT[A/G]ACTTGAAAAGACAGA | 672 |
rs528817000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053052 | CGGCTAATTTTTTGT[A/G]TTTTTAGTAGAAACG | 672 |
rs528818665 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060802 | ACGAGCCACCACACA[C/T]GACCAACATTGGCCT | 672 |
rs528851426 | in-del | -/CCCTCGCGACCTACAAACTGCCC | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125093 | TGATCCTCAGCGCTT[-/CCCTCGCGACCTACAAACTGCCC]CCCTCCCCAGGGTTC | 672 |
rs528886206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064223 | ACCCATCTTCTAGAC[A/G]CCAAGGCTAGCTATA | 672 |
rs528902306 | snp | C/T | 1.6563e-05 | 0.00287771 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124075 | TTTGTACTTCTTCAA[C/T]GCGAAGAGCAGATAA | 672 |
rs528921521 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113357 | AGCTTATTTTTCCTG[G/T]ATGTATTTTCTTTTC | 672 |
rs528921895 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053229 | AACCTGTTGATAGGA[C/G]CTGCATGCTCATAAT | 672 |
rs528926020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061431 | CCTGAATCCTACCAG[G/T]GACTTAGTTAGTCTT | 672 |
rs528958691 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116667 | GGAACTACAGGCGTG[C/T]GCCACCACGCCCGGC | 672 |
rs528978049 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109219 | CCAGTCTGGTCTCGA[A/G]CTCCTGACCTCAAGT | 672 |
rs528988246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060803 | CGAGCCACCACACAC[A/G]ACCAACATTGGCCTA | 672 |
rs528991979 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117694 | CAGTGAGCCAAGATC[A/G]CGCCACTGTACTCCA | 672 |
rs529130248 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082693 | TCACCTAGTATGGAA[C/G]TACAAGTTCTAGCTG | 672 |
rs529141553 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078937 | AGGTGATGTGGCTCA[C/T]GCCTACAATCCCAGC | 672 |
rs529147885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067379 | CCTGCCTCAGCCTCA[C/T]GAGTAGCTGGGACTA | 672 |
rs529155395 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051739 | CCTCCAGGGTTCAAG[C/T]GATTCTCCTGCCTTA | 672 |
rs529196733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123581 | TCTCGATCTCCTGAC[C/T]TCGTGATCCTACCAC | 672 |
rs529222783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084703 | GCTTCACAAAGGTTT[A/C]TACTGCTACTCTAAC | 672 |
rs529236142 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087263 | TAATAGCAAACTGTG[C/T]CTCTTACCCTGAAAC | 672 |
rs529272463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077580 | CTCAAGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 672 |
rs529293202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095239 | GACTTACCACTCCCT[A/G]TATTTAAAAACCAGT | 672 |
rs529328708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069794 | TTAGGATGAAAAATC[C/T]TAGGAAGGATATATT | 672 |
rs529393701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078232 | GGGATTATAGGTGCC[C/T]ACCACCACCCCTTGG | 672 |
rs529437412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102350 | TGCTGGGATTACAGG[C/T]GTGAAGCTTTTTTTT | 672 |
rs529450104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053892 | GAGAATCACTTGAAC[C/T]CTGGAGGCAGAGATT | 672 |
rs529494644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110051 | AGGTGCCCGCTACCA[C/T]GCCTGGCTAACTTTT | 672 |
rs529523935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101590 | TCGCTGCAACCTCCG[C/T]GTCCTAGGTTCAAGC | 672 |
rs529563897 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126383 | TGTTAGATTCACCCC[A/G]CAGAGATAGCGGCAG | 672 |
rs529600329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047465 | GAAACAGTTCATGTA[C/T]TACTTTTACAATATA | 672 |
rs529616499 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089429 | TTCTGCCTTTAGTAC[A/G]TAAACATTTCATATT | 672 |
rs529629382 | snp | C/G | 0.00169635 | 0.029074 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125326 | GGCCCAGTTATCTGA[C/G]AAACCCCACAGCCTG | 672 |
rs529640053 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080493 | TGAGCCACCGTACCC[A/G]GCAACAATATTCTTT | 672 |
rs529691620 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098583 | AGGTTATCCAGGCTG[A/G]TCTCGAACTCTGACC | 672 |
rs529695290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059486 | CAACAACAACAACAA[C/T]AACAACAACAACAAC | 672 |
rs529752382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073178 | TCTAACCCCACCCCA[A/G]ATTATCTTTTTTATT | 672 |
rs529790921 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060672 | ACCACACCATGCTAG[-/T]TTTTTTGTATTTTTA | 672 |
rs529795919 | in-del | -/TAT | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109362 | AAGCAATGAAGGTTA[-/TAT]TGGATCCAGAATTGG | 672 |
rs529854239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050180 | CAGGAGGCAAAGGTG[C/G]GTAGCTTTTGCTGTG | 672 |
rs529871415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105418 | TTATTTATTTATTTT[A/G]TTGGTAGTGATGGGG | 672 |
rs529950220 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097597 | CGTTTCTACTGAAAA[A/C]AAAAACAAAAACAAA | 672 |
rs530013712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108075 | TAGGGCTGTGCACGG[G/T]GGTCCACACCTGTAA | 672 |
rs530034380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050628 | AAAAAGAAAAAAAAA[A/T]AGAAATGTTCACCGA | 672 |
rs530063951 | in-del | -/TTT | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099277 | CTTTCTTTTGCTCTC[-/TTT]TTTTTTTTTAGATGG | 672 |
rs530074274 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099472 | GACAGAGTTTCTCCA[G/T]GTTGGCTAGGCTGGT | 672 |
rs530096735 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097841 | CTCCTAAATATCAAC[C/T]ACTATAACTATTTTT | 672 |
rs530111895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051839 | ACAGGGTTTCACCAT[A/G]TTGGTCAGGCTGGTC | 672 |
rs530117586 | snp | C/T | 0.000189161 | 0.00972341 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045028 | AGGCTGGTTTCGAAC[C/T]CCTGACCTCCAGTGA | 672 |
rs530142470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107226 | CCCAGCACCATGCCC[A/G]GCTAATTTTTTTATT | 672 |
rs530144125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100158 | AGAGTGAGACCCAGT[A/C]TCTACAAAATAATAG | 672 |
rs530178336 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052265 | TGAATGAAGAACTAA[A/C]CTTCATATTTTAATT | 672 |
rs530189179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114893 | TTCTGAAATTCTTTT[A/G]TTAAGAAACAAACAT | 672 |
rs530198737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122627 | GATTTTTAGACCATG[C/G]CTGGGTGCAATGGCT | 672 |
rs530237481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121443 | TAATCCCAGCACTTT[C/G]GGAGGCCAAGGCAGG | 672 |
rs530387939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059354 | CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 672 |
rs530393009 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090023 | CAAAGAAACCAAAAA[G/T]AAAAAAATAACTAGA | 672 |
rs530463308 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081753 | TCAGTGCTCACTTCT[C/T]ATAGGAAGTCAGCTC | 672 |
rs530464947 | snp | C/T | 1.65048e-05 | 0.00287265 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092137 | TAGGCTGTTCTAAGT[C/T]ATCTGAAATCAGATA | 672 |
rs530468884 | in-del | -/TCC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085022 | AAATTCCCCAGCAGG[-/TCC]TAAGTGGCCAAATAC | 672 |
rs530579306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066707 | AGCCACCGCGTCCAG[C/G]TGCCTCACTTGTTGT | 672 |
rs530610389 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089240 | GAAAATCACTTGATC[C/T]TGAACCTGGGAGCTG | 672 |
rs530647658 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049388 | GCCACTGATATGCCA[C/T]GTACTCTGGTTATCA | 672 |
rs530652786 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058570 | CAATCGGCTTTTCAC[C/T]TCACTGGGACTTAAT | 672 |
rs530692949 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044223 | CCCATTTTACAGAGT[A/G]GGAGACTGAAGCACA | 672 |
rs530719057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099334 | GGAGTGCAATGGTGC[A/G]ATCTCGGTTCACCGC | 672 |
rs530780378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101157 | TTTTTAGCTCTATAT[C/G]TTTTGAAAAATGAAT | 672 |
rs530881373 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127284 | TGGGGACTTGGAAAA[C/T]TTTTATGTCTAGCCT | 672 |
rs530914551 | snp | A/G | 1.65116e-05 | 0.00287324 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093809 | AGCAGATTCTTTTTC[A/G]AGTGATTCTATTGGG | 672 |
rs530919512 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101930 | TTTTTTTAAAAGATA[-/G]GGTCTCAGTCACCTG | 672 |
rs530928177 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053028 | ATTACAGGTGCACAC[C/G]ACCACACCCGGCTAA | 672 |
rs530929756 | snp | C/T | 0.000185822 | 0.00963724 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045142 | ATACCTGCCTCAGAA[C/T]TTCCTCCCCAATGTT | 672 |
rs530966522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100403 | CTGGAGTGCAGTGGC[A/G]CAATCTCAGCTCACT | 672 |
rs531010253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067295 | GAGCCTTGCTCTGTC[A/G]CCAGGCTGGAATGCA | 672 |
rs531020613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123261 | TCATTGTATGTAAAT[A/G]AGTATGTAATTTCAT | 672 |
rs531210457 | snp | C/T | 8.27383e-05 | 0.00643135 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43049125 | CCAATACTTACTGTG[C/T]CAAGGGTGAATGATG | 672 |
rs531360182 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111194 | TATTTTCTAGATTGG[C/T]ATTATTATCTTTTTT | 672 |
rs531437336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088534 | ATGTCTTCAAGGTTC[A/G]TCCATGGATGATTTT | 672 |
rs531443277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096632 | AAGGTAGGTAACATA[G/T]TTGGGGTTGCTTGTA | 672 |
rs531476168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049774 | GAGACTGTGGAGATG[C/T]TGTGTACCTGGAAAA | 672 |
rs531495665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111683 | AAAAATTAGCTGGGC[A/G]TGGTGGCAGGCGTCT | 672 |
rs531532120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062594 | GATATCCTGGTTTGC[G/T]CTGCAAAATTTTTTT | 672 |
rs531577463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121304 | GGCCTGAACCCGGGA[G/T]GCGGAGCTGGCAGTG | 672 |
rs531641677 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105897 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 672 |
rs531666844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058389 | AAAAAAACACACACA[C/T]ACACACACATAAAAC | 672 |
rs531671458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063448 | AGATAGAGAGGTCAG[C/T]GATTCACAAAAGAGC | 672 |
rs531692713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113732 | AGCCTATAATTTCCT[A/T]CTTCCACAAGTTCTC | 672 |
rs531751162 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089679 | AGCCTCCCATCTTTC[-/T]TTTTTTTTAAAGAAA | 672 |
rs531775512 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071893 | GGCGCCTGTAGTCCC[A/G]GCTACTAGGGAGGCT | 672 |
rs531782612 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108980 | CCTGGGCAACAAGAG[C/T]GAAACTCCATCTCAA | 672 |
rs531810156 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096494 | GGAGAATCGCTTGAA[-/C]CAGGGAGTTGGAGAT | 672 |
rs531832963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105477 | AACTCCTGGCCTCAA[A/G]CAATCATCCCACCTC | 672 |
rs531887715 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048258 | CCCGGGCTGGAGTGC[A/G]GTGGCGCGATCTTGG | 672 |
rs531925575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079575 | GAATTAATGTGCGTA[C/T]TGAGCACATTAAACA | 672 |
rs531944661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097484 | TTCGCCAGGCACAGT[A/G]GCTCTCACCTGTAAT | 672 |
rs531991066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072162 | GGAGGCCAAGGTGGG[C/T]GGATCACCTGAGGTC | 672 |
rs532007292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105311 | GTGCCACAATCATAG[C/T]TCACTGCAGCCTCAG | 672 |
rs532039683 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119949 | GTGAAAAGGGAAAAG[A/G]AAAAAAATTAAAATG | 672 |
rs532146262 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082055 | TAAGGAATATGTCTG[A/C]GTACTTTTTCATAGC | 672 |
rs532189201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111800 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 672 |
rs532235452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090282 | ATGGAGCTATGCAGA[A/G]TCCCTTGAATCATCC | 672 |
rs532285174 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112507 | GTCCTAGCTACTTGA[C/G]GGGCTGAGATGAGAG | 672 |
rs532324588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064346 | ATATGTGAAAGAAGA[A/G]AACAGTATTGTTGAA | 672 |
rs532348328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119746 | TTCAAAGAAATTCTC[C/T]GTAAAAGAAAAATTG | 672 |
rs532420229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049973 | CCACTATACCAAAGT[A/C]AAAAAACACTGAGAA | 672 |
rs532473191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056726 | GAGAGAAAGACACCC[C/T]AGTGAAGTGAAAAGA | 672 |
rs532485014 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105281 | GTCTTGCTCTATTGC[C/T]CAGGCTAGCATGCAG | 672 |
rs532522687 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071494 | ATCCTAGGGAGATAA[A/C]AGATATATGCAAAGG | 672 |
rs532526756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059201 | GGGCACAGTGGCTCA[C/T]ACCTGCAATCCCAGC | 672 |
rs532529710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058431 | AGAAAGAAAAAGAAT[G/T]GCTGGGCAGAGATTT | 672 |
rs532560643 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120876 | TCAAGACCAGCCTGA[C/T]CAACGTGATGAAACC | 672 |
rs532569075 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127083 | CAGGACCTGCAGCCC[C/G]CCATGCCCGAGCCCC | 672 |
rs532575889 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114808 | ACATTTAAGGTAAGA[C/T]GTGAGCCATAGCTTA | 672 |
rs532584099 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100761 | TTTTTGAGACAGAAT[C/T]TTGCTCTGTTGCCAG | 672 |
rs532666544 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43043873 | CAAGATTCAGTGTGA[A/G]AAAAACTTGACCACC | 672 |
rs532700871 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073759 | GTGTGTATATATATA[C/T]ATATATATTTTTTGA | 672 |
rs532733264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072284 | ATCCCAGCTACTGGG[C/G]AGGCTGAAGCAGGAG | 672 |
rs532779762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061629 | ATTCTGTCTCACAGG[C/T]TGGAGTGCAGTGGTG | 672 |
rs532838563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054635 | TTGTAGAGACAGGGT[C/T]TTACTATGTTGCCCA | 672 |
rs532892884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118250 | GCAGGACATCAGATA[A/G]GTCAAGGTGCTAAAA | 672 |
rs532898260 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088559 | GATTTTTGTTTATCT[C/G]TATTTTCTAAGTTTT | 672 |
rs532899955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053964 | AGAAGAGCAAAGCTT[C/T]GTCTTAAAAAAAAAA | 672 |
rs532945782 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082780 | TGATGTTAGTGAGGG[-/A]AAAAAATCCTCAAAT | 672 |
rs532984972 | in-del | -/AAAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057836 | CGAGACTCCGTCTCA[-/AAAC]AAACAAACAAACAAA | 672 |
rs533045755 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066848 | TTGAGACAAGAATCT[C/T]GCTCTTGTCCCCAGG | 672 |
rs533074710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124611 | CTACTTCCCTCTTGC[A/G]CTTTCTCAATGGCGC | 672 |
rs533137251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076146 | TAAATCAACAGCTAG[A/C]CTTTTTCTAGAAAGA | 672 |
rs533192993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078333 | CAGGTGATCCGCCAA[A/C]CTTGGCCTCACAAAG | 672 |
rs533202152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084866 | CCAAAATGCTTCACA[A/G]GCTGTATTAGTCACT | 672 |
rs533222994 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063532 | TAAGGCTTGTAGCAG[A/C]AGTTTCCTTCTGGAG | 672 |
rs533273196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067803 | GTAGCAATCCTGCAC[A/G]TTCTACACGTGTCCT | 672 |
rs533281080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077190 | GAAAAAAACAAATAA[A/G]CCCCCTAAACCAACA | 672 |
rs533285038 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048934 | AGTCTTCCCTCAGTA[C/T]ATTTAATATGTGCAG | 672 |
rs533301808 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125919 | AGAGCGGGCACAATT[C/T]TCACGGAAATCCAGT | 672 |
rs533328434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095392 | TTTGAGACCAGCCTC[A/G]GTAACATGGTGAAAC | 672 |
rs533329834 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066420 | ACTTGTTCTTTCTTT[C/T]GTTGTTGTTGAGACA | 672 |
rs533361153 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048269 | GTGCAGTGGCGCGAT[C/G]TTGGCTCACTGCAAC | 672 |
rs533401739 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088200 | CATTTTAAGTGTACA[C/G]TTCAGTGGCATTATT | 672 |
rs533447941 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121201 | TAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 672 |
rs533463117 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087456 | TCACTTGAGGCCAGG[A/G]GTTTGAGACCAGCCT | 672 |
rs533464646 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126409 | GGCAGAGCTGGCAGC[C/G]GACGGTCTTTGCATT | 672 |
rs533593602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103000 | TGTGTTGCCCAAGCT[A/G]GGCTCAAAGGACCTC | 672 |
rs533684596 | snp | A/G | 3.89848e-05 | 0.00441485 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095829 | GTGCCTGTTAAGTTG[A/G]CAAACTTTGCCATTA | 672 |
rs533769150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117319 | TGGTGGCGCATGCCT[A/G]TGGTCTCAGCTACTT | 672 |
rs533777889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047957 | TTTTGTATTTTTGGT[A/G]GAGACAGGGTTTTGC | 672 |
rs533802049 | snp | A/G | 0.000131809 | 0.00811708 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094139 | TGCCTTCTTCCGATA[A/G]GTTTTCCCAAATATT | 672 |
rs533807861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102691 | TAGATCTTGCTTTGC[C/T]GCCCACGCTGAAGTG | 672 |
rs533819030 | in-del | -/T | 0.248471 | 0.249995 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072875 | CCTGGCCCCAGCTAG[-/T]TTTTTTTTTTTTTTT | 672 |
rs533933113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055022 | CCCAAAGTGCTGGGA[C/T]CACAGGTGTGAGCCA | 672 |
rs533958766 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111388 | AGCCAGGTGTGGTGG[C/T]ACATGCCTGTAGTCC | 672 |
rs534027447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069158 | AGAGAAGCTAATGAC[A/G]TCCTCCCCCTTTTGC | 672 |
rs534033511 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108707 | GGAAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 672 |
rs534041585 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106201 | GGCACGGCGATACAG[C/T]CCTACTTTACATAAG | 672 |
rs534075660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101729 | CTGGTCTCAAACTCC[G/T]GACCTCAAATTATCT | 672 |
rs534155748 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111831 | CGTCTCAAAACAAAA[A/C]AAACAAAAACAAACA | 672 |
rs534180964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062691 | CAACCTCCACCTCCC[A/G]GGTTCAAGAGATTCT | 672 |
rs534188700 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119131 | CTAACCTGGCAGTGT[C/G]ACAAGAATGTGGTTT | 672 |
rs534231284 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075920 | AACAAGGTAAAACTC[C/T]ATCTCTACCAAAAAT | 672 |
rs534282754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115911 | AGGCCTCAAGTTCGT[C/T]CAATATTTATTAAAT | 672 |
rs534297223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103879 | TGGGGAGCCGAGGTG[A/G]GTGGATCACCTGAGG | 672 |
rs534300096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066809 | GCTCACCACCCTCCA[A/G]ACCTTTTTTTTTTTT | 672 |
rs534332225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056290 | GAGATACTCTCAACT[C/T]AGCCTTCCGAGTAGC | 672 |
rs534358756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066322 | GACTATCTCGGAGCT[A/G]TTATCAGACTTTTTT | 672 |
rs534384877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078435 | CCTTGGCATCTCACA[G/T]TGCTGGGATTATAGG | 672 |
rs534450069 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087587 | GAATCGCATGAACCC[A/G]GGAGGCAGAGGATGC | 672 |
rs534485324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081955 | GCTTTCTGTGGATCA[A/G]AGTGCAGTTCCTGAA | 672 |
rs534518690 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113808 | ACAGGGTCAGCCAGG[C/T]GCGGTGGCTTACACC | 672 |
rs534528346 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125595 | GGAAGAGGAAGAATT[C/T]TACCTGAGTTTGCCA | 672 |
rs534592646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058845 | TATTATGACTGGTCA[C/T]GGACATGAGAATAAA | 672 |
rs534602788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122904 | GAAAAAAAAATACAA[A/G]AAATTAGCCGGGCGT | 672 |
rs534608998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073367 | AAATTAAAAACAGCA[A/G]AGATGTCATCCTTGA | 672 |
rs534734759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051669 | TGAGACGGAGTCTCT[C/T]TCTGTCACCTAGGCT | 672 |
rs534741945 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119160 | TTTTTCCTTAAATAT[C/T]TAACTTTTTAGAAAA | 672 |
rs534754492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084232 | AAATGGTGTTTCACC[A/G]TGTTAGCCAGGATGG | 672 |
rs534759528 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090692 | TTCATTAAAATCAGT[A/C]TTTAGTATGCTACAA | 672 |
rs534821636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123697 | GGAGCTTGTTTTAGA[A/G]CTGGAAGAAAAGCCA | 672 |
rs534861904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100535 | GTGTGTATATATATA[C/T]ACATATATATGTGTG | 672 |
rs534865456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080805 | AGCAAGACCCTCTCT[A/G]TAAGGTGAGGCTCAG | 672 |
rs534924035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099695 | CACAAATACAAATTA[C/T]GACCAAGATTTTTGG | 672 |
rs535025564 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069066 | CGTGTTGCACAATAC[G/T]GCCATGAAGGTCAGG | 672 |
rs535071846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107166 | ACCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 672 |
rs535077186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068004 | AAGTCTCGGCTGGGC[A/G]CGGTGGCTCACGCCT | 672 |
rs535079819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060218 | AGCTGGGATTAGAGG[C/T]ACGCGCCACCACGCT | 672 |
rs535102073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116747 | TGGTCTTGAACTCCT[A/G]ACCTCAGGTGATCCG | 672 |
rs535126949 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086515 | TGTGCTACTTTAGAC[A/G]TAAGACAGCCTGAAA | 672 |
rs535139220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076308 | TCATGTTGTAGCTTA[C/T]GTTATAGGTTCAAAA | 672 |
rs535142257 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067408 | TACAGGCGCACGCGA[A/C]CACACCCAGCTAATT | 672 |
rs535142720 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075188 | CTACTTGAGTCTAAA[G/T]GGATATGTTAGAATC | 672 |
rs535180172 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43078012 | AGTGATGGGATTACA[C/G]GCGTGAGCCACTGCG | 672 |
rs535256518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066373 | ACTCAAACTAGGTGT[C/T]ACATGAAGCTGGGGT | 672 |
rs535279193 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057037 | TTTTTGTCAACTTGA[A/G]GGAGGGAGCTTTACC | 672 |
rs535382993 | snp | C/T | 1.65023e-05 | 0.00287244 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099753 | ATTATTATTAAATAC[C/T]TAAAAAACCTGAGAC | 672 |
rs535421181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052133 | CCTCTTCCACTTACA[C/G]GGCTTGGCAACACTG | 672 |
rs535462321 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116664 | GTTGGAACTACAGGC[G/T]TGCGCCACCACGCCC | 672 |
rs535469002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068074 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 672 |
rs535501913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124327 | TCTGAATTTTTTCAC[A/G]TATTGCTGCCAACCC | 672 |
rs535534924 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117895 | CTACTACTATATTCA[A/C]GTACTATTCTAGGAG | 672 |
rs535563803 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044745 | GTTTTAGAACACATT[C/T]TTTAGAAATCTAGCA | 672 |
rs535595205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117506 | CAGCACTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 672 |
rs535683597 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049284 | CCGGATGAAGGCTTA[C/T]AGCAAGACCTCTCAA | 672 |
rs535687779 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073675 | TGACTCATTTTCTAA[A/T]AAAGGACTGGCCTAA | 672 |
rs535697353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083047 | TGAAAAAAGCCCTCT[A/C]TCTATGGCATTTTAT | 672 |
rs535739898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053113 | GAACTCCTGACCTCA[C/T]GATCCACCCGCCTCA | 672 |
rs535756147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085207 | TTTATCATGTCTTTT[C/T]CTTCCATAAAGACCC | 672 |
rs535781701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122975 | GGCAGAAGAATGGCA[C/T]GAACCCGGGAGGCAG | 672 |
rs535888877 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072377 | CTGGGCAACAAGAGT[G/T]AAACTCCGTCTCAAA | 672 |
rs535947765 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112966 | GCGCCTCCACGCCCG[C/T]CTAATTTTGTATTTT | 672 |
rs535969463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069012 | TACCAAGGGCCATCA[C/T]TTACTAGCCATAGCC | 672 |
rs535976830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061084 | TGAGCCAAGATTGTG[C/T]CACTGCACTCCAGCC | 672 |
rs535977743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125016 | AGACATAGTGTCCCC[C/T]TCAAGGCATATTCCA | 672 |
rs535984309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072516 | CAAGTGATCTTCCTG[C/T]CTCAGCCTCCTGAGT | 672 |
rs535985692 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103968 | AAAAATTAGCCTGGC[A/G]TGGTGGCGCGTGCCT | 672 |
rs536008864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097048 | AAAACTGTGGGGTAT[A/G]CTTAGTACCCGGATG | 672 |
rs536073275 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096312 | AACCTGGGAGGCAGA[C/T]GTTGCGGAGAGGTGA | 672 |
rs536082149 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081525 | CTTTAACACTCAGAT[A/G]AGAATCACTGAGCTA | 672 |
rs536106876 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097518 | AGCACTTGAGGAGGC[C/T]GAGATGGGTGGATTA | 672 |
rs536146873 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056802 | CTTATCAGCTAAGAT[C/G]TGAACCCGAGACGGG | 672 |
rs536157026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075502 | GCTTACTATGGGTCA[A/G]ATACTAAGGCTAGGC | 672 |
rs536209322 | in-del | -/TTT | 0.0217236 | 0.101931 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062099 | TATGCACACACACAC[-/TTT]TTTTTTTTTAAGAGA | 672 |
rs536239640 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127455 | CAGTGCTCTGTGTCT[A/T]GCTCAAGGTTTGCAA | 672 |
rs536272925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095454 | GGGTGTGGTGGCATG[C/T]GCCTGTAGTCCCAGC | 672 |
rs536311534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057236 | GCATTCAGGCCAGGC[A/G]CAGTGGCTCACCCCT | 672 |
rs536390258 | in-del | -/AAAAAAAAAAAG | 0.477853 | 0.102875 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104059 | CAAGACTCCATCTCA[-/AAAAAAAAAAAG]AAAAAAAAAAGAAAA | 672 |
rs536511731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051532 | TCAAAGTTATTGGCT[A/G]AAGTTTGATGTTTAT | 672 |
rs536628022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073238 | GCTTATAGCAATTTT[G/T]TAAGAAAGGAAAAAA | 672 |
rs536678313 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099051 | TGGTCTTGAACTCCC[A/G]ACCTCAGGTGATCCG | 672 |
rs536727581 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105984 | ATACAAAAATTGGCC[A/G]GGCATGGTAGCGTGT | 672 |
rs536730460 | snp | C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055939 | AGTAAGACTCTGGCC[C/G/T]GAAAAATAAATTAAC | 672 |
rs536760321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066272 | TATAGGACAAATGAT[C/T]TGTCTCCTCCCTTTT | 672 |
rs536790478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113935 | CAAAAATTAGCTGGG[C/T]GTGGTGGCAGATGCC | 672 |
rs536835224 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057970 | GGTTGCTGTGAGCCA[C/T]GATCATGCCACTGCA | 672 |
rs536871129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113908 | GTGAAAACCCTGTCT[C/T]GACTAAAAATACAAA | 672 |
rs536876813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089508 | GGTGACCAAATTATT[A/G]GCCTTGACCATTAGG | 672 |
rs536942181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098174 | GGACTACAGATGCAC[A/G]CCACCACACCCAGCT | 672 |
rs536947481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071933 | GAATGGCGTGTACCC[A/G]GGAGGCAGAGCTTGC | 672 |
rs536950836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080685 | ATGGTGGTGGACGCC[C/T]ATAGTCCCAGCTACT | 672 |
rs536980757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050988 | GGAACCCCCATCGTG[G/T]GATCTTGCTTATAAT | 672 |
rs536995998 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126885 | CGCAGCGCTCGCCAG[C/T]CAGCGCGAGTTCCAG | 672 |
rs537027018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065534 | TTAGGTATGGTGGTG[C/T]ATTCCTGTAATCCCA | 672 |
rs537090491 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072716 | ACTACAGGCATAAGC[C/T]ACCAAGCCTGGCTAA | 672 |
rs537311780 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127189 | CCCATCGACTGCCCA[A/G]GGGCTGAGAGGAGTG | 672 |
rs537337342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099501 | GTCTCGAACTCCCGA[A/C]CTCAGGTGATCCACC | 672 |
rs537514613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123011 | GCAGTGAGCTGAGAT[C/T]GCGCCACTGCACTCC | 672 |
rs537542014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084208 | GCTAATTTTTTGTAT[G/T]TTTAGTAGAAATGGT | 672 |
rs537555686 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060046 | AAGTAGCTGTGATTA[C/T]AGGCACATGCCACCA | 672 |
rs537597375 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102739 | CTCACTGTAGTCTAC[A/T]TCTCCTGGACTCAAG | 672 |
rs537603936 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099103 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCT | 672 |
rs537666395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110248 | AAGGTTGTTAACTAA[A/G]CTTAAAAGAAAATGA | 672 |
rs537703484 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044427 | GTCCTTCCAACAGCT[A/G]TAAACAGTCCTGGAT | 672 |
rs537737635 | snp | C/T | 8.27315e-05 | 0.00643109 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091919 | TAATTTCTTGGCCCC[C/T]CTTCGGTAACCCTGA | 672 |
rs537778783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051871 | CGAACTCCTGACCTC[A/G]TGATCTGCCTGTCTT | 672 |
rs537805724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087621 | GAGCCAAGGTCACAC[C/T]ACTGCACTCCAGCCT | 672 |
rs537806106 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096380 | AGACTCTGTCTCAAA[A/G]AAAAAAAAAAAAAAG | 672 |
rs537848419 | snp | G/T | 0.000164715 | 0.0090736 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057010 | AGTGGAATACAGAGT[G/T]GTGGGGTGAGATTTT | 672 |
rs537869341 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103987 | TGGCGCGTGCCTGTA[A/G]TCCCAGCTACTAAGG | 672 |
rs537941409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078479 | GCCTGGCCAAGGCGG[A/T]AATATTTAATAAGTA | 672 |
rs537975637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050241 | AAGGCCTTTGTGCTG[C/T]GCAACTCCAGAGGTA | 672 |
rs538013523 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072861 | AAGCCACCCACCACG[A/C]CTGGCCCCAGCTAGT | 672 |
rs538015792 | in-del | -/TCTC | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051664 | TTTTTTGAGACGGAG[-/TCTC]TCTCTGTCACCTAGG | 672 |
rs538026991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054164 | GGGAAGAATCTGGTG[C/T]TAATACTGCCTAGCA | 672 |
rs538030364 | snp | C/G | 0 | 0 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063000 | GGTTCAAGTGATTCT[C/G]CTGCCTCAGCCTCCC | 672 |
rs538094577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070208 | AAAGTGCTGGGATTA[C/T]AGGCTTGAGCCACCA | 672 |
rs538109895 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048440 | TCGATCTCTTGACCT[C/T]GTGATCTGCCCACCT | 672 |
rs538111910 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066183 | TGTACTCAGATTTAG[C/T]TTATAGTCAACTAAA | 672 |
rs538329982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097127 | AACAAACTGCACATA[A/C]ATCCCTGAACCTAAA | 672 |
rs538334824 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126762 | GGAGCCCTTCAGCCC[A/G]CCACTGCGCTGTGGG | 672 |
rs538378944 | in-del | -/AAC | 0.270621 | 0.249148 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100618 | ATATAACATATATAT[-/AAC]ATATATATATGTTAT | 672 |
rs538407629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095648 | TTACAGAAGGTCTTA[C/T]TATAGGTACATTAGT | 672 |
rs538461450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103204 | GGGCTTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 672 |
rs538463270 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118847 | TGGCTCACTGCAACC[C/T]CTGCCTCTCGGATTG | 672 |
rs538573388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119282 | TCAAAAAAAGAAAAA[A/G]AAAAAAGAAAAGGAT | 672 |
rs538604240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079111 | AGGCTGAGGCGGACA[C/T]TGTAATGAGCCGAAA | 672 |
rs538644113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050940 | AGAGTGGTAGAGAAA[C/T]AGAATAGCCTCTAGA | 672 |
rs538655691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088673 | ACATCATTCACTTAC[G/T]AGCAGCTAAAAGGGT | 672 |
rs538692389 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065485 | ACCAGCCTGACTGAC[A/T]TGGAAAAACCCTGTC | 672 |
rs538796028 | in-del | -/TTC | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069934 | GAAATATTCACGCAA[-/TTC]TTCTTCTTATTATTG | 672 |
rs538833843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048503 | AGCCACCGCACCTAG[A/C]TTTTCTCTCTCTCTC | 672 |
rs538904644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050309 | TGTCAAGTTTAATTA[G/T]AAAATGTTCATGGAG | 672 |
rs538914067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096249 | GGGTGTGGTGGCGCG[C/T]GCCTGTAGTCCCAGC | 672 |
rs538918222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057617 | GAGACAGGCGGATCA[C/T]GAGGTCAGGAGATCG | 672 |
rs538963430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113773 | TATTCATAACTTAAT[C/T]TCTCTTTTTTTGTTA | 672 |
rs538969920 | snp | C/T | 3.31005e-05 | 0.00406807 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049201 | CCAGTTGATCTAAAA[C/T]GGACATTTAGATGTA | 672 |
rs539044217 | snp | A/G | 2.04866e-05 | 0.00320045 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045615 | AGCTCCCAGGGCCTG[A/G]AAAGGCCACTTTGTA | 672 |
rs539072195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105578 | GAACCCTGCCCAATC[C/T]CTCACTTAGTTCTGC | 672 |
rs539167487 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072730 | CCACCAAGCCTGGCT[A/G]ATTTTGTATTTTTAG | 672 |
rs539183859 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046509 | TTCAAGCGATTCTCC[G/T]GCCTCAGTCTCCCAA | 672 |
rs539184339 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112864 | GCTGGAGTGCAATGG[C/T]GCAATCTCGGCTCAC | 672 |
rs539202364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064742 | AGTAACATTTATTAC[A/T]CTTAAAAACTTCAGT | 672 |
rs539224787 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120142 | AAAACAACAACCCAC[C/T]GGGGAACACATTTTA | 672 |
rs539340412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104780 | GACTAAAAGGTCTTA[A/T]CACCACGTCATAGAA | 672 |
rs539366179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060223 | GGATTAGAGGCACGC[A/G]CCACCACGCTGGGCA | 672 |
rs539425640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069880 | CCCACTACTGAATCC[A/G]TTTGATAATCTGGTA | 672 |
rs539429322 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061815 | GTCTCGAACTCCTGA[C/G/T]CTCAAGTGATCCACC | 672 |
rs539454967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100654 | TATATAACATATATA[C/T]AACATATATATATAT | 672 |
rs539455017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109281 | GGATTACAGGCATGA[A/G]CCATCAAGCCTGGCC | 672 |
rs539474284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117966 | AGAGCTCATATTCTA[A/G]TGTGGTAGACAGTTG | 672 |
rs539489361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069068 | TGTTGCACAATACTG[C/T]CATGAAGGTCAGGCC | 672 |
rs539523845 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111337 | CCAGCCTGGCCAACA[A/T]AGTGAAACCCCGTCT | 672 |
rs539571067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054310 | CAGAAGGTAAAAACA[A/G]GCTGACCTCAGCAGT | 672 |
rs539643756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116022 | TATATTGATCCCTTC[A/G]ATACTCTATACTATC | 672 |
rs539670699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060899 | GGGAGGTTGAGGTGG[C/T]TGGATCACTTGAGTT | 672 |
rs539682857 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074929 | CTGTCAAGAAAGAAA[G/T]GAAAGGAAAGAAAGG | 672 |
rs539719696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108565 | ACAAAATTAGCCAGG[C/T]GTGGTGGGCACACGC | 672 |
rs539733232 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125088 | CTTCCTGATCCTCAG[A/C]GCTTCCCTCGCGACC | 672 |
rs539820050 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075975 | GCGCATGCTTGTGGA[A/C]CCAGCTACTCAGGAG | 672 |
rs539845430 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125475 | TCTCAGAATACGAAA[G/T]CAAGGTACAATCAGA | 672 |
rs539882124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054917 | ACCACGCCCAGTTAA[C/T]TTTTGTATTTTTAGT | 672 |
rs539937727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062629 | TTTAAGACGGAGTCT[C/T]GCTCTGTTGCCAGGT | 672 |
rs539960293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118583 | TGAGCCACCATGCCA[A/G]CCATCTTTTTAATTT | 672 |
rs540031582 | snp | A/G | 0.00049554 | 0.0157329 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044985 | ATTTCTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 672 |
rs540032771 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077260 | TCTTAAATAATACAT[A/G]GAACTAATGATGAAA | 672 |
rs540069793 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114744 | CATAGTTTGTACCTG[A/G]TACCAGGTTATGTAC | 672 |
rs540186719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106633 | ATAATCTCACAACTG[C/T]CCTTAAGAGCCATTT | 672 |
rs540193654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095230 | CTATCTACAGACTTA[A/C]CACTCCCTATATTTA | 672 |
rs540266584 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096521 | AGATTGCAGTGAGCC[A/G]AGATGGCGCCACTAC | 672 |
rs540305323 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064035 | CTAAAGAGCCTCAGT[C/T]TTTTACACTCCCAAG | 672 |
rs540324604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095697 | ATCAGACCATACCAC[A/G]ACATTTGACAGAGAA | 672 |
rs540330350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076710 | TCAAAAGCATCAATC[C/T]ATGATACACAAATTG | 672 |
rs540368789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087202 | GGAAATAATCAGGGA[C/T]GTAGGCAAATATTTA | 672 |
rs540373654 | snp | C/T | 1.6596e-05 | 0.00288058 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124000 | TCCCAAATTAATACA[C/T]TCTTGTGCTGACTTA | 672 |
rs540411088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061308 | TCCTTAAACGAAAGT[A/T]ATCAACAACCTTTGA | 672 |
rs540414384 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052880 | GACAAGTCTGTGTGT[G/T]TTTTTTTTTTTTTTG | 672 |
rs540444229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108818 | ACCAACACGGAGAAA[A/C]CCTGTCTCTACTAAA | 672 |
rs540451983 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100097 | CACTTTGGGAGGCTG[C/G]AGCAGGACTGCTTGA | 672 |
rs540476162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117601 | AAAACTAACTGGGCA[C/T]GGTGGCATGCGCCTG | 672 |
rs540485703 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057830 | AACTGAGCGAGACTC[C/T]GTCTCAAAACAAACA | 672 |
rs540488323 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120306 | AGGCTGAAAACCTTA[C/T]CTACCCTATAGCTAC | 672 |
rs540499276 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073564 | AAACTCTGATTTACA[A/C]GCCATAAAACACCAT | 672 |
rs540507798 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102171 | CACCTCCCGGGTTCA[A/T]GCTATTCTCCTGCCT | 672 |
rs540511191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060981 | AAATAAAAACTAGTC[A/G]GGTGTGGTAGCACGC | 672 |
rs540585820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053863 | AATCCTAGCTACTTA[A/G]GAGGCTGAGGCAGGA | 672 |
rs540613262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048225 | TCTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 672 |
rs540643971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102841 | AAAACTTTTAATATA[C/G]ACAAGGACTTGCTAT | 672 |
rs540725941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099166 | TCTAGTACAATTTAT[C/T]TTGGAACTAAATACT | 672 |
rs540776004 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124497 | ACCAACACCAATCAA[A/G]GCCTCCCCGCCCCTA | 672 |
rs540809803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065031 | GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 672 |
rs540855647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108104 | AATCCCAGCACTTGC[A/G]GGGTGGGTGAATCAC | 672 |
rs540873151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071995 | CCTGGGCAACAGAGC[A/G]AGACTCCGTCTCAAA | 672 |
rs540876009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054571 | CAGCCTCCTGAGTAG[A/C]TGGGAATACAAGAGT | 672 |
rs540946680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065588 | AGAATCGCTTGAACC[C/T]GGGAGGGGGAGGTTG | 672 |
rs540952111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114050 | ACTGCACTCCAGCCT[A/G]GGCAATAGAGTGAAA | 672 |
rs540971735 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118008 | AAGAATACATGGGAA[G/T]AAGTGCATTAAAGAG | 672 |
rs540989685 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048359 | AGGCGTGCGCCCCTA[C/T]GCCCAGCTAATTTTT | 672 |
rs541121833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052239 | ATTGAGCACTGGAGA[C/T]GTGGTTAGGGTGAAT | 672 |
rs541138085 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081611 | CCTAGTGGGGACCCC[A/G]TGCCTAGCATCTCCT | 672 |
rs541212318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116104 | TGATATATTTTTCTG[C/T]ACTATCACTGTGGGT | 672 |
rs541237054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120495 | TTAAGGCCGGGCGCG[A/G]TGGCTCACGCCTGTA | 672 |
rs541281969 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122547 | ATAGAAGATAAAGTG[A/T]GTGCTGGGGGTGTGG | 672 |
rs541337178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057491 | ACTCCAGCCTGGGTA[A/G]CAGAGCGAGACTCCA | 672 |
rs541362276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113565 | GTAGAGACAGTGTTT[C/T]GCCATTTTGGCCAGG | 672 |
rs541420533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067019 | GACGGGGTTTCAACA[C/T]GTTGGCCAGGCTGGT | 672 |
rs541449811 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079458 | GTTCAAAAAGGAATG[A/C]CCCACAAGTGTTACC | 672 |
rs541512953 | snp | C/T | 1.6473e-05 | 0.00286988 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43082464 | CAGAAGAGTCACTTA[C/T]GATGGAAGGGTAGCT | 672 |
rs541592598 | in-del | -/A | 0.252702 | 0.249985 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114074 | GTGAAACACCATCTC[-/A]AAAAAAAAAAAAAGA | 672 |
rs541642139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081237 | GGATGGGACTCTGAT[C/T]TCTCATTATCTGAGA | 672 |
rs541711460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051699 | TGGAGCGTAGTGGTG[C/T]GATCTGGGCTCACTG | 672 |
rs541744841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059058 | GGAGTCTAGTGATAA[A/G]TTTGTCAGAAGACTC | 672 |
rs541824546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116979 | TAGCCTTATTTCCTA[C/T]AAACTAGACTTACAG | 672 |
rs541909701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045945 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 672 |
rs541968959 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048288 | GCTCACTGCAACCTC[C/T]GCCTCCGGGGTTCAA | 672 |
rs542045501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083678 | AGGGAAGGATCCAAC[A/G]GAAAGAGCCCTGAGA | 672 |
rs542050423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114218 | GGTTATGGGCAGGAG[C/T]TACCACACTGGGCCC | 672 |
rs542159969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067280 | TTTTTTTTTGAGACG[A/G]AGCCTTGCTCTGTCG | 672 |
rs542163374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123137 | TCTGGAGGCTGAGGT[A/G]GGAGGATTGCTTGAG | 672 |
rs542209256 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108095 | CACACCTGTAATCCC[A/T]GCACTTGCGGGGTGG | 672 |
rs542219734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048263 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 672 |
rs542231412 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063685 | TATAAAAGAGACCCA[-/T]TTTTCCCAGCATCAC | 672 |
rs542231656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060476 | TACAGGTGTGAGCCA[C/T]TGTGCCCGAACCTTT | 672 |
rs542235377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055945 | ACTCTGGCCCGAAAA[A/C]TAAATTAACAAAGAA | 672 |
rs542257356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067500 | ATCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 672 |
rs542262166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111678 | TACAAAAAAATTAGC[C/T]GGGCGTGGTGGCAGG | 672 |
rs542280731 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111529 | GTCTCAAAACAAAAC[-/A]AAAAAAAAACAGCCG | 672 |
rs542280896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060072 | CACCATTCCCAGCTA[A/T]TTTTTTTTTGTTTTT | 672 |
rs542293286 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115338 | GAAACCTTATCTCTA[C/G]TAAAAGTACAAAAAT | 672 |
rs542317419 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077166 | ACATTTTCAATTACC[A/G]AAAAAAAAGAAAAAA | 672 |
rs542356303 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052971 | AACCTCCACCTCCTG[G/T]GTTCAAGTGATTCTC | 672 |
rs542437045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073832 | TGATCTTGGCTCACC[A/G]CAACCTCCGCCTCCC | 672 |
rs542450918 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083184 | TCTTTCTTTCTTTTT[C/T]TTTTTAAGTCTCCCT | 672 |
rs542471357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119021 | TCCATCTGCCTCGAC[C/T]GGGATTACAGGCGTG | 672 |
rs542471390 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126280 | GCCACCAGTCAATGG[A/G]GTGGTCGTTTTGAGG | 672 |
rs542522579 | in-del | -/TAGCACTT | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058109 | TCACACCTATAACCC[-/TAGCACTT]TAGCACTTTGGCACT | 672 |
rs542687218 | snp | A/G | 6.59011e-05 | 0.00573988 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43104137 | CAAGGAAGGATTTTC[A/G]GGTTCACTCTGTAGA | 672 |
rs542693151 | in-del | -/ATA | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070072 | TGAGTAGCTGGGATT[-/ATA]ATAGGCATGCGCCAC | 672 |
rs542750606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112271 | ATTTTTGTATTTTTA[A/G]TAGAGATGGTGTTAC | 672 |
rs542759505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056627 | TCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCT | 672 |
rs542781277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078696 | GATTTCCTGAGTTAG[A/T]CTTCAAATGCATTAT | 672 |
rs542805568 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120503 | GGGCGCGGTGGCTCA[A/C]GCCTGTAATCCCAGC | 672 |
rs542844842 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050435 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAA | 672 |
rs542917948 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070487 | CTTACAAGCCAGGAT[C/G]AAAACAAACACTAGA | 672 |
rs542961527 | in-del | -/AAAAAAAAAAA | 0.440195 | 0.162252 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096376 | GCAAGACTCTGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA | 672 |
rs542981338 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072117 | TACAGGCCGGGTGCG[G/T]TGGCTCAGGCCTGTA | 672 |
rs542991600 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126995 | GGTGCGCCGGGTCCC[C/G]CAGCACTGCCGGCCC | 672 |
rs543090430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065020 | TATTTTTACTAGAGA[C/T]GGGGTTTCACCGTGT | 672 |
rs543102980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121267 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 672 |
rs543150283 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105241 | AAACTAGAGTACTTT[A/T]TTTTTTGTTTAATTT | 672 |
rs543189924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120592 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 672 |
rs543196221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089112 | GAGGTCAGGAGTTCG[A/G]GACGAGCCTGGCCAA | 672 |
rs543228232 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116471 | CCTGGGCTCAAGCAA[C/T]CCTCCCAGCACGGGG | 672 |
rs543238533 | snp | C/T | 7.41909e-05 | 0.00609015 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079306 | AATTTGCCAAAATGA[C/T]GAACACAAAGGGAAA | 672 |
rs543267121 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119764 | AAAAGAAAAATTGGA[A/T]TCAGTTATCATACCA | 672 |
rs543275480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112329 | CTGACCTCGTGATCC[A/G]CCCACCTCAGCCTCC | 672 |
rs543282256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070636 | ACCTACTTGCTTTTA[C/T]AGATAGAAAGGAAAA | 672 |
rs543313238 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120453 | ACTTTCCATACAAAT[G/T]AATGTAAAACACCAT | 672 |
rs543320922 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122730 | CATGGCCAACATAGC[-/A]AAACCCTATCTCTAC | 672 |
rs543339349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089968 | ACCATGACTGCACTA[C/T]TCCATTCCAGCCTGG | 672 |
rs543566267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050538 | GAATCACTTGAACCC[G/T]GGAGGTGGAGGTTGC | 672 |
rs543578116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122384 | GCAACTAGGTCCCAA[C/G]TACCGTTCTAACTAC | 672 |
rs543589933 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126378 | CGCCATGTTAGATTC[A/C]CCCCACAGAGATAGC | 672 |
rs543667709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098243 | GCTATGTTGCCCAGG[C/G]TGGTCTCAAACTCCT | 672 |
rs543749843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119625 | GATAACTTGTACCAA[A/C]ATTGGTATTATTACT | 672 |
rs543766104 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065865 | TCTCTTCCGGGTAAC[A/G]GTTCTTCAGATACTT | 672 |
rs543819165 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087572 | GAGGCTGAGGCAGGA[A/G]AATCGCATGAACCCG | 672 |
rs543827703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068480 | CTTTGGGAAGCTGAG[A/G]TGGGAGGACTGCTTG | 672 |
rs543828720 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054427 | TAAAGGGACAGAAAG[G/T]GCTCAGTAGAAGGAT | 672 |
rs543852008 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082145 | GAGCAAGAGCTATGT[C/T]GTATACCATGTATCT | 672 |
rs543867657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072995 | GTACTGAGATTACAG[A/G]CATGAGCAGTGGCTG | 672 |
rs543890833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077164 | TCACATTTTCAATTA[C/T]CGAAAAAAAAGAAAA | 672 |
rs543983254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114356 | CCCAGGGCTTTAAAG[C/G]TTAATCTTTAGCTCT | 672 |
rs544009377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090112 | GCTAGATGGTCTCTA[C/T]TAGGAAGAGAACCCT | 672 |
rs544063733 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112842 | AGTTTTCACTCTTGT[C/T]GCCCAGGCTGGAGTG | 672 |
rs544103365 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062895 | AGCCACTGCACCCGA[-/T]TTTTTTTTTCTTTTG | 672 |
rs544120795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081164 | ATTATAATTGAAAGT[C/T]TAGTCTGTGTTTAGA | 672 |
rs544156209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088117 | ACAGGAATACTAAAA[G/T]AATATACACCAATAA | 672 |
rs544192586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077829 | ACCTCTCTGCCTCCC[A/C]GGTTCAAGCTGTTCT | 672 |
rs544240711 | snp | A/C | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126173 | AATGCGCTCTGGCCC[A/C]TGTCTGCGCACTCGT | 672 |
rs544293039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078886 | AGGAACCATATCAAA[C/T]GGAATTAACCATTGG | 672 |
rs544293226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088896 | GTGCTGGGAATACAA[A/T]GAACCAACCTAATTA | 672 |
rs544342552 | snp | A/G | 0.000185891 | 0.00963903 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125293 | CAGAGCAGAGGGTGA[A/G]GGCCTCCTGAGCGCA | 672 |
rs544382811 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060567 | TGCGATCTTGGCTCA[C/T]TGTAACTCCTACCTT | 672 |
rs544408856 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096186 | GTTCAAGACCAGCCT[A/G]GCCAACATGGTGAAA | 672 |
rs544413754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101995 | GCAGCCTTGACTCTC[C/T]ATGTTAAAGCAATGC | 672 |
rs544453284 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103334 | TAGCCAGGTCTGGTG[C/T]CGTACCCCTGTAGTC | 672 |
rs544465176 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048930 | AAAAAGTCTTCCCTC[A/T]GTATATTTAATATGT | 672 |
rs544505961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085632 | CTCCTCTTTTTCCAC[C/T]TGGAAAAATTCTCAT | 672 |
rs544528686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055179 | TGAAATCTTGCAGAC[C/T]TTCTCCCTGTGAGGA | 672 |
rs544602997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048246 | CTCGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 672 |
rs544607338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095721 | CAGAGAATGATACTC[C/T]AACTCTGCCAAGAGA | 672 |
rs544617033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102877 | CCAAACTGGTCTTGA[A/G]CTCCTGAGCTCAGGC | 672 |
rs544660181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118123 | CACTGAGGTGAGACT[A/G]GAGGATAGCTTAATA | 672 |
rs544822119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110743 | ATTTTGGGAGGTGGA[G/T]GTGGGCGGATCACTT | 672 |
rs544857747 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125344 | ACCCCACAGCCTGTC[C/T]CCCGTCCAGGAAGTC | 672 |
rs544909272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085792 | CGGAACTGGTCTGGA[A/G]GGAAGCAGAGTGTAT | 672 |
rs544988610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070395 | TGAAGCAATTCCCAT[C/T]TCTGGCATTAAGGAC | 672 |
rs545047287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089609 | CTGGAGAGCAGCAGC[A/G]TGATCTCAGCTCACT | 672 |
rs545051960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078525 | AAATTGCAAAAGTCT[C/T]CTATTCATTAAAAAG | 672 |
rs545069609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069462 | TGCCTTTGCCAAGAA[A/T]GATTAGACCATTTTA | 672 |
rs545107728 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071293 | ATGTTGAATTACAAA[A/G]TTCTGGTCTCTGTTA | 672 |
rs545115509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118985 | TGCCCAGGCTGGTCT[C/T]GAAGTCCTGACCTCA | 672 |
rs545160227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086979 | GAATGGGCAGTAGAA[G/T]ATAAGCCTTCTCTAA | 672 |
rs545169555 | in-del | -/CAA | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062422 | TGAAGAGCTTTTCTT[-/CAA]CAACAGTGAACAGTT | 672 |
rs545179019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049030 | CTTCTGAGGCTACAG[G/T]AGGGGCATCCATAGG | 672 |
rs545223577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43094965 | CCAACTGGCTATATT[A/G]GAGAAACTAACCTCA | 672 |
rs545254044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056470 | AGGAACGAGCCGCTG[C/T]GCCTGGCCCAGTGAA | 672 |
rs545421339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089003 | ACTTGGAAAATTTTG[A/G]TGCCACTTCTACAAA | 672 |
rs545472402 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126932 | CGGGCCCCGCACCCC[A/C]GGCCCCGGGCAGTCA | 672 |
rs545486238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084478 | GCTTCAAAATATACA[C/T]GTTTAAAAATCACTT | 672 |
rs545560355 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126465 | TGGTAAGGAAGCAGC[A/C]TGGGTTAGCTAGGGG | 672 |
rs545578139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051770 | GCCTCCTGAGTAGCT[A/G]GGATTACAGGCGCGC | 672 |
rs545638799 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096910 | CTCCACTATAAAATG[A/C]GAGAACTAAACTAGA | 672 |
rs545715000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052207 | GCTAATAAGGTAGCC[A/G]TGAGTCACATATAGT | 672 |
rs545720734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059105 | CCTTGTACCCCTGAG[C/G]TTCATACAATGTGTC | 672 |
rs545723152 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051581 | GTACTCACTATGACC[C/T]CATCAACAGAGGGGT | 672 |
rs545736576 | snp | A/G | 4.94474e-05 | 0.00497205 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093457 | AAGTATCGCTGTCAT[A/G]TCTTTTACTTGTCTG | 672 |
rs545752115 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102113 | TCTCACTCTGTCGCC[C/T]AGGCTGGATCGCAGT | 672 |
rs545815302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101250 | TGCCCAGGCTGGAGC[A/G]TGGTGGCGTGATCTC | 672 |
rs545835005 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123332 | TACCTATCCTCTCAA[A/C]GACACCGATCATCCA | 672 |
rs545931469 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108949 | AGTAAACTGAGATCG[C/T]GCCATTGCACTCCAG | 672 |
rs545943348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099363 | GCAACCTCCACCTCC[C/T]GGGTTCAAGTGATTC | 672 |
rs546018673 | snp | C/T | | | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044135 | TGCAACAATTTGTTT[C/T]GGCAGCAACAGGAAA | 672 |
rs546044312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107088 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 672 |
rs546073815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109062 | TATCTACCTACCTAT[C/G]TATCTGTCTACAGTC | 672 |
rs546153705 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098098 | GGCATGATCATAGCT[C/T]ACTACAGCCTCAAAC | 672 |
rs546185232 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049980 | ACCAAAGTAAAAAAA[C/T]ACTGAGAAATCCTTG | 672 |
rs546202759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053776 | GGAGTTCAAGACCAG[C/T]GTGACCAACATGGAG | 672 |
rs546220308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061278 | TCAATTTTTTCAGAA[A/G]GGCTTTCCCTGGCCT | 672 |
rs546227617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117016 | TCATTCAGGTTCAAC[C/T]TTCTGGCAAGAACAC | 672 |
rs546238440 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074178 | AAACCTTGATTAACA[A/C]TTGAGCTATTTTTCT | 672 |
rs546346507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108433 | TACCCTCTCTTGGCC[A/G]GGTGCAGTGGCTCAT | 672 |
rs546408259 | snp | C/T | 8.25171e-05 | 0.00642275 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076651 | AAATCTACTTTACTG[C/T]TTTGTTCTGATAGTG | 672 |
rs546463310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117558 | AGCCTGGCCAACACA[A/G]TGAAACGCTGTCTCT | 672 |
rs546575174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074104 | CCTCATCCTCAAAAT[C/T]ATTAGTTAAACCATT | 672 |
rs546601519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123532 | TTTTTGTATTTTTAG[C/T]GGAGAGGGGGTTTCA | 672 |
rs546613713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059630 | TACTAACAAGATCTA[C/T]TGTTCAAGCCAAAAC | 672 |
rs546643185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117076 | GATCACTTCAGAAGA[A/G]GCATGATGTTTGGTT | 672 |
rs546648076 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065044 | ACCGTGTTAGCCAGG[A/C]TGGTCTCGATCTCCT | 672 |
rs546660277 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124874 | CGATTCTCCTGCCTC[A/C]GCCTCCTGAGTAGCT | 672 |
rs546697677 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097874 | AATGCCTGTTGTCTA[C/G]GAATTTATGATCATA | 672 |
rs546871298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083935 | GTGGTGCGATCTTGG[C/T]TCACTGCAACCTCCG | 672 |
rs546887123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122911 | AAATACAAAAAATTA[A/G]CCGGGCGTGGTAGTG | 672 |
rs546916793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052617 | GTTTTGGGTGACTCT[C/T]AGTGTCTTGACCTTC | 672 |
rs546931422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101449 | ATCCACCCGCCTTGG[C/G]CTCCCAAAGTGCTGG | 672 |
rs547070218 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077425 | AACCTCCACCTCCTG[A/G]GTTCAAGCGATTCTC | 672 |
rs547196117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103863 | TGTAATCCCAGCAAT[C/T]TGGGGAGCCGAGGTG | 672 |
rs547204017 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096389 | CTCAAAAAAAAAAAA[A/G]AAAAAGAGAGAAAGA | 672 |
rs547204407 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082118 | TTCTCCCATTCCACT[G/T]AGCTTCCAATAGAGC | 672 |
rs547216067 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120594 | CACGGTGAAACCCCG[A/T]CTCTACTAAAAATAC | 672 |
rs547282583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112539 | TTGCTTGAACCCAGA[C/T]TGCAAGGTAAAAGTG | 672 |
rs547286231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046071 | GAATTACAGGCACAT[A/G]CCATCACACCCAGCT | 672 |
rs547331043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079672 | AGAGAAAGGTACGTG[A/G]GTTCAACTGAAGCAC | 672 |
rs547334043 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096250 | GGTGTGGTGGCGCGC[A/G]CCTGTAGTCCCAGCT | 672 |
rs547334118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104433 | AATCAACTGGAAATT[C/T]TACTCCTAGGAAACA | 672 |
rs547453216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051406 | CTCACTTTTGTCACC[A/T]ATCAGGCCAAGGCTC | 672 |
rs547482120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106397 | CTATGTTATTAAATA[A/T]TTTCTACTTTTTCCT | 672 |
rs547519830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058547 | AATCTTTTGTGTGCA[C/G]AACTTAACAATCGGC | 672 |
rs547566236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120894 | ACGTGATGAAACCCT[A/G]TCTCTACTAAAAATA | 672 |
rs547588639 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109211 | TATATTGCCCAGTCT[C/G]GTCTCGAACTCCTGA | 672 |
rs547593667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049252 | ATACTTAACCCAGGC[A/C]CTCTACCCTACACTC | 672 |
rs547611609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056243 | CAGTGGCGCAATCTC[C/T]GTTCACTGTAGTCCC | 672 |
rs547915046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107143 | GATCTCGGCTCACTG[C/T]AAGCTCCACCTCCTG | 672 |
rs547956153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098920 | CTTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 672 |
rs547983558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065121 | AGGCCTGAGCCACCA[C/T]GCTTGGCATCTTTTT | 672 |
rs548055373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050641 | AAAAGAAATGTTCAC[C/T]GAGAATCTTCCCCTG | 672 |
rs548062048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090555 | AATTTTTGTATTTTT[A/C]GTAGATGTGGGGTTT | 672 |
rs548079593 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057864 | AAACAAACAAAAAAA[A/C]CAAAAATTAGCTGGG | 672 |
rs548088133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105419 | TATTTATTTATTTTG[C/T]TGGTAGTGATGGGGT | 672 |
rs548163236 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082973 | TTGGTGTTGTGAGAT[C/T]CATCAGACATTTAGG | 672 |
rs548181949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080562 | GTAACCCCAGCACTT[C/T]GGGAGGCTGAGGTGA | 672 |
rs548275991 | snp | C/G/T | 0.000167771 | 0.00915737 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044392 | TGCCCTTGCACACTG[C/G/T]GGGGGCTAGGGAAGA | 672 |
rs548359710 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122695 | GGGTAGATCACTTGA[A/G]GTCAGGAGTTTGAGA | 672 |
rs548363680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114931 | TCAAAAGACAAGATC[A/C]TCAAATACGTAAATA | 672 |
rs548497799 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115789 | TCCAGACTAGCAGGG[G/T]AGGGGGGGAGAAAAA | 672 |
rs548565272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107254 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 672 |
rs548599438 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072110 | ATAAGAGTACAGGCC[A/G]GGTGCGGTGGCTCAG | 672 |
rs548603222 | in-del | -/CTAT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109058 | TATCTATCTACCTAC[-/CTAT]CTATCTGTCTACAGT | 672 |
rs548628532 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116887 | TTTTTAAAATTAGGT[C/T]ATTTGACCTGTGGAG | 672 |
rs548639961 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073845 | CCGCAACCTCCGCCT[C/T]CCGGGTTCAAGTGAT | 672 |
rs548641533 | in-del | -/AAAT | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072026 | AAAATAAATAAATAA[-/AAAT]AAATAAATAAATAAA | 672 |
rs548650583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051850 | CCATGTTGGTCAGGC[C/T]GGTCTCGAACTCCTG | 672 |
rs548683050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083068 | GGCATTTTATAAAAA[C/T]ACAACAAATATAAAA | 672 |
rs548702456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100265 | ATTATGTATTATTTG[C/T]GTAATTTTTGAAGTA | 672 |
rs548750620 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125367 | AGGAAGTCTCAGCGA[A/G]CTCACGCCGCGCAGT | 672 |
rs548758718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117801 | CAAGTTCCCATCCCT[A/G]CCTGTCTATCCACAA | 672 |
rs548763916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058657 | AGACTGCTAATACTG[C/T]GCTGTTATAAAGGTA | 672 |
rs548764898 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080269 | TTAAGGAAGACACTG[C/G]AAGACAACAGATATT | 672 |
rs548847425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103710 | CCACTTAATATACCA[C/T]CTTTCCTTCTTCACT | 672 |
rs548900754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059364 | AGCTACTCGGGAGGC[C/T]GAGGCAGGAAAATCA | 672 |
rs548929885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064634 | AAACACAGCAGGCTA[C/T]CTGCAAGCAGCAGCA | 672 |
rs548991214 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073225 | TTGGGGGCAATGAGC[-/T]TATAGCAATTTTGTA | 672 |
rs549001917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054707 | TGGCCTCCTAAAGTG[C/T]TGGGATTACAGAAGT | 672 |
rs549037251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110196 | ACCGCACCCGGCCTC[A/G]AATCTTTCTTTATGC | 672 |
rs549136682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071447 | TAACACGTATTTACA[C/T]TTTCAGTCAACAATG | 672 |
rs549142144 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095586 | GACCCCATCTCAAAA[A/G]AAAACAAACAAACAA | 672 |
rs549174508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061669 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG | 672 |
rs549174540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069582 | AGTGATCAAGAGCCA[C/T]TGAAACAGACACAGG | 672 |
rs549196936 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051778 | AGTAGCTGGGATTAC[A/G]GGCGCGCACCACCAC | 672 |
rs549235896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068806 | TGTTACTAAAGGTCA[A/G]TGCAAAAGCGATCAA | 672 |
rs549332987 | snp | A/G | 0.000746686 | 0.0193077 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125312 | CTCCTGAGCGCAGGG[A/G]CCCAGTTATCTGAGA | 672 |
rs549384372 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126571 | CGTGTCTCCGGACAG[C/T]TAATCGTTTTAGTGA | 672 |
rs549464143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113642 | AAAGTGCTGGTATTA[G/T]AGGCGTGAGCCACCG | 672 |
rs549529369 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072365 | TTGCACTCCAGCCTG[A/G]GCAACAAGAGTGAAA | 672 |
rs549537973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121444 | AATCCCAGCACTTTC[A/G]GAGGCCAAGGCAGGA | 672 |
rs549542396 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112679 | TTATATGTATACACA[C/T]ACATATATCTTTATG | 672 |
rs549577188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111259 | GCAAGGTGGCTCATG[C/T]CTGTAATCCTGGCAC | 672 |
rs549640262 | snp | C/T | 4.94205e-05 | 0.0049707 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070952 | TGGGGTCAGGCCAGA[C/T]ACCACCATGGACATT | 672 |
rs549649481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096738 | TGAAGTCCTTGAACA[A/T]TTTCATCAGTCACAA | 672 |
rs549676175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063485 | AGAATGACAGAGGAG[A/G]GGTCCTTCCCTCTAA | 672 |
rs549707401 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125963 | ACCTGTGCGCGCTTG[A/T]ACTTGTCAACAGTTA | 672 |
rs549732504 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057605 | CTTTGGGAGGCCGAG[A/G]CAGGCGGATCACGAG | 672 |
rs549752602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096211 | GTGAAACCCCATCTC[C/T]ACTAAAAATACAAAA | 672 |
rs549762124 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079524 | CATGCTGTTGGCATC[A/G]CTGTAAACAAGTTAA | 672 |
rs549870405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050800 | GGCACTAACAGCAGC[A/T]CAACGCCATCTGAAC | 672 |
rs549881847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079074 | GCGTGGTGGCGGGTG[C/T]CTGTAATCCCAGCTA | 672 |
rs550000982 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048972 | ATCCTTACCCATCCC[A/T]TACAGATGGAGTCTT | 672 |
rs550013330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103824 | TGAAAATGGTTTTAC[C/T]GGCCGGGCACAGTGG | 672 |
rs550126981 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060810 | CCACACACGACCAAC[A/G]TTGGCCTATCTTTTA | 672 |
rs550145636 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064290 | CCATGTCAATAGTTT[C/T]GATTAATGTGGACGG | 672 |
rs550188653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060220 | CTGGGATTAGAGGCA[C/T]GCGCCACCACGCTGG | 672 |
rs550210077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113743 | TCCTTCTTCCACAAG[A/T]TCTCAAAGCAACTAT | 672 |
rs550233933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097906 | GGGGGGAAAACAGTA[A/G]GTGTTATGATAAATA | 672 |
rs550272207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053314 | CAAAAGATTAGGAAT[A/G]TTTATATCCAGGCTA | 672 |
rs550302666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071527 | TAGTCATAGGAATAG[C/T]ATAATTTTAGAAACA | 672 |
rs550348364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105483 | TGGCCTCAAGCAATC[A/G]TCCCACCTCAGCCTC | 672 |
rs550355170 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058791 | TGATAAAATATACAT[C/T]CAATGCACTAAAGAA | 672 |
rs550369539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101627 | TGTGCCTCCGCCTCC[C/T]GAGTAGCTGGGATTA | 672 |
rs550394029 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047120 | CTTTTTTCTTTTTGA[-/G]ACACGGTCTCGCTCT | 672 |
rs550443374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064720 | TAACTGCTACAAAAG[C/G]CGATTTAGTAACATT | 672 |
rs550468294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112756 | AACCAAGCTTCTCAC[G/T]CTTCTCCAGTTGCCA | 672 |
rs550525916 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085134 | TACTTCTACTATGCT[C/G]CTCTGATCTCTACTT | 672 |
rs550533612 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121232 | TACAAAAAATTAGCC[A/G]GGCATAGTGGTGGGC | 672 |
rs550582771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117210 | ACTTTGGGAGGCTGA[A/G]GTGGGTGGATCACCT | 672 |
rs550585693 | snp | G/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127291 | TTGGAAAACTTTTAT[G/T]TCTAGCCTGAGGATT | 672 |
rs550608894 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089260 | CCTGGGAGCTGAAGG[G/T]TGCAGTGAGCCAAAA | 672 |
rs550612733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123586 | ATCTCCTGACCTCGT[C/G]ATCCTACCACCTTGG | 672 |
rs550622250 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095272 | GTAAAAGATGAAACA[C/T]AAATACACCAATTAA | 672 |
rs550653698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069051 | TCACACCAGTATTTA[C/T]GTGTTGCACAATACT | 672 |
rs550721308 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109260 | CCTTGGCATCCCAAC[C/G]TGCTGGGATTACAGG | 672 |
rs550810402 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053909 | TGGAGGCAGAGATTG[C/T]GGTGAGCCAAGATCA | 672 |
rs550813494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084171 | GAGTAGCTGGGATTA[C/T]AGGCGCCCGCCACCA | 672 |
rs550840298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076072 | CAATCTAGGTGACAC[A/G]GGGCGACCCTGTCTC | 672 |
rs550843001 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086114 | ATCACATACATACAC[A/T]CACACACACACACAC | 672 |
rs550940657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046264 | AGACGGAGTCTTGCT[C/G]TTGTTGCTCAGCCTG | 672 |
rs550948341 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120970 | TCAGGAGGCTGAGGC[A/C]GGAGAAGCGCTTGAA | 672 |
rs551044712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069823 | TTAATAAAGATATTT[C/T]AGAATGACTTGGTCA | 672 |
rs551078372 | snp | C/T | 1.64857e-05 | 0.00287099 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047712 | GGACACCCTGGATCC[C/T]CAGGAAGGAAAGAGC | 672 |
rs551131416 | in-del | -/AC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058377 | GACTCTGCTAAAAAA[-/AC]AAACACACACACACA | 672 |
rs551138669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047552 | TTTAAAATGTGCCAA[G/T]AACTGTGCTACTCAA | 672 |
rs551153577 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055039 | ACAGGTGTGAGCCAC[C/T]GCGACCAGCCTGGGA | 672 |
rs551194188 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054639 | AGAGACAGGGTCTTA[C/T]TATGTTGCCCAGGCT | 672 |
rs551267064 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126868 | TGGGAACTGGGGCTG[C/T]GCGCAGCGCTCGCCA | 672 |
rs551335995 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117872 | TATAACAAGTGTTTA[C/T]TAAGTATCTACTACT | 672 |
rs551394520 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060902 | AGGTTGAGGTGGTTG[G/T]ATCACTTGAGTTCAG | 672 |
rs551395404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069936 | AATATTCACGCAATT[A/C]TTCTTCTTATTATTG | 672 |
rs551400929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061642 | GGCTGGAGTGCAGTG[A/G]TGCAATCTAGGCTCA | 672 |
rs551404275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110130 | CGATCTCCTGACCTC[A/G]TGATGTGCCCATCTC | 672 |
rs551423678 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088903 | GAATACAAAGAACCA[A/G]CCTAATTATTAGAAG | 672 |
rs551457931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062652 | TGCCAGGTTGGAGTG[C/T]AGTGGCACGATCTTG | 672 |
rs551476469 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127091 | GCAGCCCGCCATGCC[C/T]GAGCCCCCTCCCAAC | 672 |
rs551480129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118584 | GAGCCACCATGCCAG[A/C]CATCTTTTTAATTTT | 672 |
rs551539164 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126952 | CCGGGCAGTCAGGGG[C/T]CTAGCACCCGGGCCA | 672 |
rs551539557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119751 | AGAAATTCTCCGTAA[A/G]AGAAAAATTGGATTC | 672 |
rs551548887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110899 | TGAGGTCAGGAGTTC[A/G]AGATCAGCCTTGTCA | 672 |
rs551570928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067961 | TTTTTCTCAGAAAGG[A/G]TACATTTAAAAAATT | 672 |
rs551636483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076210 | AGAAGTCTACCATCA[C/G]TTTCCAAGCTTGTTC | 672 |
rs551653468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078355 | CTCACAAAGTGCTGG[A/G]ATTATAGGCATGAGC | 672 |
rs551694493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124716 | CTCTTCTTCCACAAG[A/G]TCCCATCCTCTCATA | 672 |
rs551711908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086542 | GAAATCTGACTTCAA[C/T]GGTTTTGGGTAGATG | 672 |
rs551772007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082666 | AAATTAATTTTAGCA[C/T]AGGAATTGAAATCAC | 672 |
rs551781454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088228 | ATTTTCACACTGTTG[C/T]GTTACCATTGCCACT | 672 |
rs551781613 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125923 | CGGGCACAATTCTCA[A/C]GGAAATCCAGTGGAT | 672 |
rs551891813 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125677 | ACAGTAATTGCTGTA[C/G/T]GAAGGTCAGAATCGC | 672 |
rs551930387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090319 | GGCTCCTTTTTCTCA[C/T]CTCTCTTGATACAGT | 672 |
rs551975491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095438 | CCACAAAAAATTAAC[C/T]GGGTGTGGTGGCATG | 672 |
rs552000394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051316 | ACACTACTGGATTTC[A/C]GAAGATCTTCTTGAA | 672 |
rs552026104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122845 | AGGTCAGGAGATCAA[A/G]ACTATCCTGGCTAAC | 672 |
rs552049686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081825 | CAGAGGTCCATCTGG[A/T]TTTTTTTTGATAACT | 672 |
rs552060143 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060922 | CTTGAGTTCAGGAGT[C/T]TGAGACCAGCCTGAC | 672 |
rs552129370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121558 | TGTGATGGCACATGC[C/T]TGCAATCCCAGGTAC | 672 |
rs552162044 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090200 | ATTGGTGAGAGTTCT[A/G]TACCTGGCTGTGTGG | 672 |
rs552246630 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084221 | ATTTTTAGTAGAAAT[G/T]GTGTTTCACCGTGTT | 672 |
rs552364009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107309 | ACCTCGTGATCTGCC[C/T]GCCTCTGCCTCCCAA | 672 |
rs552371242 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090648 | CCAAAGTGCTGGGAT[A/T]AGCAAATGGGTTTCG | 672 |
rs552439674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100501 | CGTGTGCAACTATGC[C/T]TGGCTAATTTGTGTG | 672 |
rs552499204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108259 | ATGAGAATAAGTTGA[A/G]CCTGTGAGGCGGGGG | 672 |
rs552502832 | snp | A/C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067399 | AGCTGGGACTACAGG[A/C/T]GCACGCGACCACACC | 672 |
rs552505690 | snp | C/T | 3.30256e-05 | 0.00406346 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093818 | TTTTTCGAGTGATTC[C/T]ATTGGGTTAGGATTT | 672 |
rs552527524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059498 | CAACAACAACAACAA[C/T]AACAACAACAACAAC | 672 |
rs552589615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045993 | GATGGCGCAATCTCG[A/G]CTCATTCAACCTCCG | 672 |
rs552636154 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084883 | CTGTATTAGTCACTA[C/T]TGTCACAACCATCAC | 672 |
rs552648003 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045162 | TCCCCAATGTTCCAC[A/T]CCAACATTTGAGAAC | 672 |
rs552657801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051686 | CTGTCACCTAGGCTG[C/G]AGCGTAGTGGTGCGA | 672 |
rs552681627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099181 | CTTGGAACTAAATAC[C/T]GTAGCAATCCATCAT | 672 |
rs552684496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106790 | GTTATGATCACATAA[A/C]ACTTAATAAAAGTTA | 672 |
rs552699049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075166 | CACTCACTCTATACA[A/C]AATATTCTACTTGAG | 672 |
rs552731089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058895 | AAATTTGAGGAAGAA[C/T]GCTCAGAAACAATTC | 672 |
rs552774490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051927 | GGCATAAGCCACTGC[A/G]CCCGGCCCTCTCTGA | 672 |
rs552911643 | snp | C/T | 0.000343466 | 0.0131002 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044492 | GCAAGCAAAATTATT[C/T]ATGAAGCTGTATGGT | 672 |
rs552911736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052527 | TCTCATAAACACACT[G/T]GCATAGGTTCTTAGC | 672 |
rs552932910 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060231 | GGCACGCGCCACCAC[A/G]CTGGGCAAATTTTTG | 672 |
rs552946046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115331 | ATATGGTGAAACCTT[A/C]TCTCTACTAAAAGTA | 672 |
rs552947216 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123764 | TGCAGAACCAATCAA[C/G]ACAGAGTCCCTGTCT | 672 |
rs553002761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117398 | AGAGTGAGCCAATAT[C/T]GTGCCACTGCACTCC | 672 |
rs553060066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124233 | AGGTTTTAGAATAAT[A/G]CAAACCAAAGAACTA | 672 |
rs553061285 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107505 | CGTGCCTCAGCCTCC[A/C]GAGTAGCTGGGATTA | 672 |
rs553144112 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108852 | ACAAAAATTAGCCGG[C/G]CATGGTGGCATATGC | 672 |
rs553201733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121191 | CCATCTTGGCTAACA[C/T]GGTGAAACCCCGTCT | 672 |
rs553346156 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126240 | GGGTTCAGCTTGCTT[C/T]TGCCCCGTCTCCGTC | 672 |
rs553428986 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083497 | GCAAAAAGCTAATTC[A/G]TGAATCTATCTGTTT | 672 |
rs553456571 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126771 | CAGCCCGCCACTGCG[C/G]TGTGGGGGCCCCTCT | 672 |
rs553608949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084276 | ACCACATGATCCTCC[C/T]GCCTCGGCCTCCCAA | 672 |
rs553643790 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044586 | GGATCTGTCATTTTA[C/T]AGATATGAAATATTC | 672 |
rs553655568 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070261 | TATTATGAAGTGATG[A/G]CAATGACAATTAATT | 672 |
rs553765213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088727 | GAAGCCACAGCAGGA[A/T]GAATCGAGGGGGTCT | 672 |
rs553786319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112173 | CAACTCACTGCAGCC[A/T]CTGCCTCCTGGGTTC | 672 |
rs553903746 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071720 | AAAAATAAAAGTTTA[C/T]GGGCCGAGCACGGTG | 672 |
rs554018985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078568 | GTAATTCATTTTGAG[C/T]TTTTATTAGAAAAGC | 672 |
rs554026214 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072556 | CACAGGTGTTTGCCA[C/T]CTTCCAGCTGATTTT | 672 |
rs554045950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057208 | GAAGTGGAGCAGACA[C/T]GTCATATTTAAGGCA | 672 |
rs554050881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048522 | TCTCTCTCTCTCTTT[C/T]TTTTTTTTTTTAGAC | 672 |
rs554065020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112889 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 672 |
rs554141394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089858 | GTAAAAACTTAAAAA[C/T]TAGCTGGAGGTGTTG | 672 |
rs554143285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120422 | AAAGGAAGTGAAATA[A/T]GATCCCTATCCTAGA | 672 |
rs554173106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050310 | GTCAAGTTTAATTAG[A/T]AAATGTTCATGGAGA | 672 |
rs554178320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050965 | TCTAGAACATTTCAG[C/T]AATCTGAGGAACCCC | 672 |
rs554213438 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098131 | CTGGGTTCAATGTAT[C/G]CACTCACCTCTGCCT | 672 |
rs554255600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120943 | GTGGCGTGCGCCTAT[A/G]ATCCCAGCTACTCAG | 672 |
rs554281750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071877 | GCTGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 672 |
rs554282444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080099 | AGAGTCCAAGTTTCA[A/G]AATATTATTGTAGTT | 672 |
rs554304339 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126869 | GGGAACTGGGGCTGC[A/G]CGCAGCGCTCGCCAG | 672 |
rs554307369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049620 | AATACCATACTTGGT[A/G]GTAATTACTGTAAAT | 672 |
rs554343538 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088797 | AGAACATAAGCAAAC[G/T]GTCTAAGATCACATA | 672 |
rs554370716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056521 | TTATTGGCTGGGCAC[A/G]GTGGCTCACGCCTAT | 672 |
rs554373226 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114391 | GTAAATACTGGGACT[-/T]TTTTTTTTTTTTTTT | 672 |
rs554473317 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105684 | GGGTTTAGTAAAGTG[G/T]AATTAAAGCACAATT | 672 |
rs554490981 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076042 | AGGATGCAGTGAGCC[A/G]TGACTGCACCACTGC | 672 |
rs554557150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064909 | GATCTCAGCTCACGG[C/G]AAGCTCTGCCTCCTG | 672 |
rs554694722 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057240 | TCAGGCCAGGCGCAG[G/T]GGCTCACCCCTGTAA | 672 |
rs554696342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065435 | GCACTTTGGGAGGCC[A/G]AGGTAGGTGGATCAC | 672 |
rs554747061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073680 | CATTTTCTAATAAAG[G/T]ACTGGCCTAAAACTT | 672 |
rs554790483 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099023 | AGATGGGGTTTCTCC[A/T]TGTTGGTCAGGCTGG | 672 |
rs554849044 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126295 | GGTGGTCGTTTTGAG[A/G]GACAAGTGGTAAGAG | 672 |
rs554853276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105840 | ATACATTGTGTTTGT[A/G]TAAATAATTAGATAG | 672 |
rs554889085 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108072 | CACTAGGGCTGTGCA[C/T]GGTGGTCCACACCTG | 672 |
rs554891835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079210 | AAAACAAAAAAAATG[A/G]AAGGCAGAGGGAAGG | 672 |
rs554926201 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073413 | GCCATGGTATCAGGA[A/G]TTAAGCATAGCTAAG | 672 |
rs555051911 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112420 | ATAACATTCAAAACA[C/G]AATTTAAAATATGGC | 672 |
rs555064806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122087 | TTTGTTTAGCTATAA[C/T]GTTGAAGGGCAAGGG | 672 |
rs555068216 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085568 | CACATGACAACTTTA[C/T]GTTTCCTGGGAATTC | 672 |
rs555106894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048026 | TTCACCCCCGGGATT[A/T]TAGGCATGAGCCACC | 672 |
rs555140905 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109808 | CAGTAGAGTGACAAG[C/T]TAAGCTGTCTCGTGC | 672 |
rs555142905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082243 | GTCCCTCTGACTGGT[A/G]TATTAGTTGTGAGCA | 672 |
rs555179190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050469 | ATACAAAAAATTAGT[C/T]GGGCGTGGTGGCACA | 672 |
rs555207554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099054 | TCTTGAACTCCCGAC[C/T]TCAGGTGATCCGCCC | 672 |
rs555228568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058014 | GACAGAGTGAAACTC[C/T]GTCTCAAAAAAAAAA | 672 |
rs555270550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049299 | TAGCAAGACCTCTCA[A/G]TGGGAGAGTCTGTCT | 672 |
rs555315616 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056330 | AAGTACATGCCACCA[C/T]GCCTGGCTAATTTTT | 672 |
rs555405401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096321 | GGCAGACGTTGCGGA[A/G]AGGTGAGATCACACC | 672 |
rs555468034 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111889 | TTTCAGAACTTTAGG[C/G]TTGCTTGGGTCAATA | 672 |
rs555491898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061908 | TACTTTCACATTTCA[C/T]TTTGCCTGATCTGTT | 672 |
rs555501364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053629 | CCGAGACGGCGCCAC[C/T]GCACTCCAGCCTGGG | 672 |
rs555530019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109518 | GGGTCCTTCTTCGCC[A/G]ATATAGATGCTTCAA | 672 |
rs555607249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103967 | CAAAAATTAGCCTGG[C/T]ATGGTGGCGCGTGCC | 672 |
rs555629174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062813 | TGTTGCCCAGGCTGA[C/T]CTCGAACTCCTGAGC | 672 |
rs555631493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070168 | GATCTCCTGACCTTA[A/G]GTGATCTGACCACCT | 672 |
rs555739266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115448 | CGGAGGTTGCAGTGA[C/G]CCAAGATCATGCCAC | 672 |
rs555942071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069166 | TAATGACATCCTCCC[C/G]CTTTTGCTACCACCC | 672 |
rs555951369 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126023 | GAAAGCAGAAACTAG[G/T]CCTTAAAAAGATACG | 672 |
rs555977909 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081573 | GGGAGTACTCACCAC[C/T]CCTGCATGTTTCTAA | 672 |
rs555994106 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125599 | GAGGAAGAATTCTAC[C/G]TGAGTTTGCCATAAA | 672 |
rs556018307 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085981 | GGCTTTATCATGCTA[A/G]TTTTGTCGACATGTT | 672 |
rs556032779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125214 | AAATCCACTCTCCCA[C/T]GCCAGTACCCCAGAG | 672 |
rs556107698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050246 | CTTTGTGCTGCGCAA[A/C]TCCAGAGGTAAGCTT | 672 |
rs556117109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047035 | ATGCCTGGTGGAGTT[A/T]TATGGTGATCATCTC | 672 |
rs556189797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118908 | AGCTGGGACTACAGG[C/T]GCGTGCTGCCACACC | 672 |
rs556216804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087667 | AACTCCATCTCAGAA[A/G]AAAAAAAAAAAAAAG | 672 |
rs556218466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070245 | GCCATGCAATTATTT[C/T]TATTATGAAGTGATG | 672 |
rs556228451 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125642 | TAGCCTCTACTCTTC[C/T]AGTTGCGGCTTATTG | 672 |
rs556307724 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055246 | ATCAGGAGAAAGTCA[C/G/T]TGAGTCTTCTTGGGT | 672 |
rs556333401 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102740 | TCACTGTAGTCTACA[A/T]CTCCTGGACTCAAGT | 672 |
rs556365659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048159 | CCTTGGCCTCCCAGT[G/T]TTGTGATTACAGGGG | 672 |
rs556393295 | in-del | -/AAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104096 | GAAAAGAAGAAGAAG[-/AAG]AAGAAGAAAACAAAT | 672 |
rs556426278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054219 | TGGCTCACATGGCGC[C/T]CCCCTGTGGTAAAGG | 672 |
rs556457706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119317 | AGAAAAGCTTGTGGA[C/T]AGTAACCTTATTGTG | 672 |
rs556481355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086946 | GCTTCAGGTCTAGAG[C/G]GATTTGCTCTGTACA | 672 |
rs556511632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052693 | CTTCAAAGAGACTGC[A/G]ATAGAGAAAAAAATC | 672 |
rs556572895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052140 | CACTTACAGGGCTTG[G/T]CAACACTGTTCAAAA | 672 |
rs556607494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104714 | AGGTGTGAGACCAGT[A/G]GGAGTAATTTTTTAA | 672 |
rs556653436 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044783 | CTCAGACTTTTAGAA[A/G]TCTCTTCTAGTTTCA | 672 |
rs556684572 | snp | C/T | 4.94539e-05 | 0.00497238 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092951 | CTTTGAAACCTTGAA[C/T]GTATTCTGCAAATAC | 672 |
rs556742808 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111295 | GAGGCCAAGGCGAGC[A/T]GATCACCTGAGGTCA | 672 |
rs556748364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063015 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGAATTA | 672 |
rs556776893 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050101 | CACTCATCTGCCTGT[A/G]ACCAGATGCTAAGGC | 672 |
rs556791648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111583 | TCCCAGAACTTAGGG[A/G]GGCCAAGGCGGGCAG | 672 |
rs556869186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104033 | GACTGCTTCTAGCCT[A/G]GGCCACAGAGCAAGA | 672 |
rs556930746 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112066 | ATTTCATGAAAAAGT[C/T]GATCTATCACATGGG | 672 |
rs556933975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117511 | CTTGGGAGGCCGAGG[C/T]GGGCGGATCATGAGG | 672 |
rs556949757 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107576 | TAGTTTCACCATGTT[A/G]GCTAGTCTTGAACTC | 672 |
rs556985117 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108520 | CCAGCCTGGCTAACA[A/T]GGTGAAACCCTGTCT | 672 |
rs557030603 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045455 | GGTGAAAAATTACCA[C/T]AATTTTGTGCTCATG | 672 |
rs557068480 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109636 | TTAAAACTCAGAATA[C/G]AGGCTCCCACTCCTT | 672 |
rs557068797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117950 | TAAAGCCTGCTCTCA[C/T]AGAGCTCATATTCTA | 672 |
rs557074022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066920 | CCTCCTGGGTTCAAG[C/T]GATTCTGCTGCCTCA | 672 |
rs557136254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084405 | TCCTGACCTCAGGTG[A/G]TCTGCCCGCCTCGGC | 672 |
rs557137578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074218 | TTAATTAAGTATAAC[A/G]AAAGTGTCCATGATA | 672 |
rs557149560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102007 | CTCTATGTTAAAGCA[A/G]TGCTCCAGCCTCAGC | 672 |
rs557273028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085321 | GCTGAGATCGTGCCA[C/T]GGCACTCCAGCCTGG | 672 |
rs557311876 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047783 | ATCATTTTTTTTGTT[C/T]GTTTTTGAGACAGGG | 672 |
rs557311943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046599 | TAGAGATGGGGTTTC[G/T]CCATATTGGCCAGGC | 672 |
rs557349657 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057692 | TACAAAAAAATTAGC[C/T]GGGTGTAGTGGCAGG | 672 |
rs557352041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067513 | CCCGCCTCGGCCTCC[C/T]AAAGTGCTGCGATTA | 672 |
rs557386198 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073323 | CACCATTACTTTTTT[C/G]ACTTAATAAATCAGC | 672 |
rs557399986 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102519 | GTGCCACCACACCCA[C/G]CTAATTTTTGTATTT | 672 |
rs557411042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075585 | TTTTTTGTTTTGAGA[A/C]GGAGTCTTGCTCTGT | 672 |
rs557485744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053726 | TGTAATCCTAGCACT[C/T]TGGGAGGCCGAGGTG | 672 |
rs557522467 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050230 | ATACACACACCAAGG[C/T]CTTTGTGCTGCGCAA | 672 |
rs557616849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084523 | AATGGTTGCCAAAAA[G/T]TCCAGTGGGGGAGTA | 672 |
rs557700938 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059944 | GGAGTCTTGCTCTTT[C/T]GCCCAGCCTGGAGTG | 672 |
rs557793857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101665 | GTGCCACCACACCCA[G/T]CTAATTTTTGTATTT | 672 |
rs557800624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103278 | TCGAGACCAGCCTGA[A/C]CAATATGGTGAAACC | 672 |
rs557821217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085514 | TGGTATTATCTCTCA[C/T]TTCTCCCAACACCCC | 672 |
rs557863668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102805 | CTACAGGCACACACC[A/T]CCATGCCCAGATAAT | 672 |
rs557870937 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122037 | CTCTGATTTTCAATA[A/G]ATTGATAAATTGTGA | 672 |
rs557927921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116728 | TTTCACCATGTTGGC[C/T]GGCTGGTCTTGAACT | 672 |
rs557974259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054997 | TCAGGTGATCCACCC[A/G]CCTTGGGCTCCCAAA | 672 |
rs557977822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107810 | AAAGTGGATCATAGA[C/T]CAGAAGTAGAGAGAG | 672 |
rs558002856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111348 | AACATAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 672 |
rs558018891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067405 | GACTACAGGCGCACG[C/T]GACCACACCCAGCTA | 672 |
rs558027799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069110 | ATGTTGCCTCACTCC[A/G]TACTGCCACAGGGCA | 672 |
rs558055879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100719 | TAATCCCAGCACTTT[A/G]GGATATATGTGTATA | 672 |
rs558098399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054476 | ACAAGGTCTCACAAT[A/G]TTGGCCAGGCTGGAG | 672 |
rs558127058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110464 | GGTGGTGTGCACTTA[C/T]AGTCCCAGCTACTTG | 672 |
rs558135126 | in-del | -/CTTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081883 | TATTGCATAATTAGG[-/CTTT]CTGTGTTGTTCTTTT | 672 |
rs558167701 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061820 | GAACTCCTGACCTCA[A/T]GTGATCCACCTGCCT | 672 |
rs558260007 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106885 | GTAGTTCATGTAAGA[G/T]GCTTATAATTAGTTT | 672 |
rs558264852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105996 | GCCGGGCATGGTAGC[A/G]TGTGCCTGTAGTCCC | 672 |
rs558287061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048213 | TTTCTCTCTCTCTCT[C/T]TTTTTTTGAGACGGA | 672 |
rs558289248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080723 | CTAAGGCAGGAGGAT[C/T]GCTTGAGGAGGTCGA | 672 |
rs558343167 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083842 | AAGGAGTTTTCCAAA[A/G]TATCCTTCTTAAGAA | 672 |
rs558363990 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057294 | GCAGGCAGATCACTT[C/G]AGGTCAGGAGTTCGA | 672 |
rs558378156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124505 | CAATCAAGGCCTCCC[C/T]GCCCCTAACCTTTCC | 672 |
rs558425392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072810 | CTCAGGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 672 |
rs558475369 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095681 | AGTACCATTTAAATC[A/T]ATCAGACCATACCAC | 672 |
rs558495450 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125113 | GCGACCTACAAACTG[A/C]CCCCCTCCCCAGGGT | 672 |
rs558625354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058801 | TACATTCAATGCACT[A/G]AAGAAAGTTAGAGGT | 672 |
rs558739431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116024 | TATTGATCCCTTCAA[C/T]ACTCTATACTATCAT | 672 |
rs558778499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066982 | GCCACCACGCCCACC[G/T]AATTTTTATATTTTT | 672 |
rs558788751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123012 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 672 |
rs558819698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120455 | TTTCCATACAAATGA[A/G]TGTAAAACACCATAA | 672 |
rs558892818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099107 | GGATTACAGGCGTGA[A/G]CCACTGCGCCTGGCA | 672 |
rs558978558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123674 | TTTATTTTGCCATTT[C/T]AAGTGATGGAGCTTG | 672 |
rs559010985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083270 | AAGCGATTCTCCCAC[C/T]TCAGCCTCTCAAGTA | 672 |
rs559090519 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083198 | TTTTTTTAAGTCTCC[C/T]TCTGTCACCCAGGTT | 672 |
rs559127960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087725 | AGCTAGATTATAATG[C/T]ACAGAATTATCTGGA | 672 |
rs559136129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065037 | GGGTTTCACCGTGTT[A/G]GCCAGGATGGTCTCG | 672 |
rs559190752 | snp | C/G/T | 6.59217e-05 | 0.00574078 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43092669 | TCTGAACTGAGATGA[C/G/T]AGACAAAACCTAGAG | 672 |
rs559213693 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120582 | CATCCTGGCTAACAC[C/G]GTGAAACCCCGTCTC | 672 |
rs559234080 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057538 | ATTAAAAATAAAATT[A/T]AAAAAAAAAAAATTA | 672 |
rs559237536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051610 | GTCTATGTTGATTTT[A/G]GGTGTACATGCTCCT | 672 |
rs559280434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082298 | TTACCCATGTGCTGA[A/G]CAAGGATCATAAAAT | 672 |
rs559325369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051212 | TCAAAAAACAGACTT[A/T]CAAAAAGGAAGAGCT | 672 |
rs559402783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105344 | TTCTGTACTCAAGCT[A/G]TCCTCCCACTATAGC | 672 |
rs559448041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051807 | ACGCCCGGCTAATTT[C/T]TGTATTTTTAGTAGA | 672 |
rs559467457 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123441 | CAGCAACATCTGCCT[A/C]CTGGTTCAAGTGATT | 672 |
rs559482319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121437 | CGCCTGTAATCCCAG[A/C]ACTTTCGGAGGCCAA | 672 |
rs559522690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056814 | GATCTGAACCCGAGA[C/T]GGGAATCCAAATTAC | 672 |
rs559553352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106075 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 672 |
rs559599400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058315 | GGAGTTGGAGGCTGC[A/C]GTGAACTGTGATCAT | 672 |
rs559622059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120540 | GGAGGCCGAGGTGGG[C/T]GGATCACGAGGTCAG | 672 |
rs559644370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122580 | ATTTTAAATAGGGGT[A/G]TCTGGAAATGAAAAG | 672 |
rs559734761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060056 | GATTACAGGCACATG[C/T]CACCATTCCCAGCTA | 672 |
rs559795082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052249 | GGAGATGTGGTTAGG[A/G]TGAATGAAGAACTAA | 672 |
rs559799246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067048 | GTCTCGAACTCCTGA[C/T]CTCAGGTGATCCACC | 672 |
rs559813595 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107996 | TAGGTAGGGAGTAAA[G/T]AGCAGACACTGACAA | 672 |
rs559835836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100144 | CCAGCATAAGCAACA[A/G]AGTGAGACCCAGTCT | 672 |
rs559888867 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118993 | CTGGTCTTGAAGTCC[G/T]GACCTCAAGTGATCC | 672 |
rs559980804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055742 | AGTGAGCTGAGATTG[C/T]GCCACTGCACTCCAG | 672 |
rs560007132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111614 | ATCACGAGGTCAGGA[A/G]ATCGAGACCATCCTG | 672 |
rs560073798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110966 | ATTAGCCATGCATGG[C/T]GGTGCACGCCTGTAA | 672 |
rs560098593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086990 | AGAAGATAAGCCTTC[G/T]CTAATTGTAGTTCTC | 672 |
rs560118426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062179 | GCTCACTGCAGCCTT[G/T]AACTCCTGGGCTCAA | 672 |
rs560189356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064413 | TCACCCCTAGAATGT[C/T]TACCTGGGGAGTCCT | 672 |
rs560191335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072002 | AACAGAGCGAGACTC[C/T]GTCTCAAAAAAATAA | 672 |
rs560197308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064058 | CTCCCAAGATCAATC[C/T]GGATTTATGATTCTA | 672 |
rs560218193 | in-del | -/ACA | 0.453818 | 0.144769 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059469 | GAACGAGATGCTGTC[-/ACA]ACAACAACAACAACA | 672 |
rs560232624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118283 | TAATAATCCAGGAGG[A/T]TATTGTAGGGAAAGA | 672 |
rs560246055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103557 | TCAAACCTGGACTCA[A/C]GTGATCCTCCCATTT | 672 |
rs560276844 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071422 | ATATGGCATTATGTA[C/G]CAAACACCTTAACAC | 672 |
rs560287183 | snp | C/G | 1.81358e-05 | 0.00301124 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079410 | CGAATCTGTAAGAAA[C/G]GTGAAATTGTAGACA | 672 |
rs560390912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077314 | AAAACATACTGAAGG[C/T]AAAGTTCTGGCATGT | 672 |
rs560446489 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108619 | CTGAGGCATGAGAAT[C/G]ACTGGAACCCAGGAT | 672 |
rs560462237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069522 | CAAAGGGATAAAGAA[C/T]GCTAATTTTCAATGA | 672 |
rs560475302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068741 | ACAGATATACATGGC[A/T]TAAAACCAAGACTCA | 672 |
rs560477491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077946 | CTCCATGTTGGTCAC[A/G]CTGGTCTCGAACTCC | 672 |
rs560480468 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126478 | GCCTGGGTTAGCTAG[A/G]GGTGGGGTCACGTCA | 672 |
rs560516490 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071420 | AAATATGGCATTATG[G/T]AGCAAACACCTTAAC | 672 |
rs560590835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089037 | AAATTAGGAGGCCAG[C/G]CCTGGTGGCTCACGC | 672 |
rs560592253 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119760 | CCGTAAAAGAAAAAT[A/T]GGATTCAGTTATCAT | 672 |
rs560592336 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126938 | CCGCACCCCCGGCCC[C/T]GGGCAGTCAGGGGCC | 672 |
rs560661816 | snp | C/T | 3.77615e-05 | 0.00434503 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095834 | TGTTAAGTTGGCAAA[C/T]TTTGCCATTACCCTT | 672 |
rs560794411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096627 | TAAGGAAGGTAGGTA[A/G]CATAGTTGGGGTTGC | 672 |
rs560796663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096473 | GCTACTCGTGAGATT[C/G]AGACAGGAGAATCGC | 672 |
rs560816000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049729 | CATGCTGAGCTGGAA[G/T]CCATATACTCAGGGG | 672 |
rs560864310 | in-del | -/CTGGGATTACAGGCA | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060622 | CAGCCTCTGGAGTAG[-/CTGGGATTACAGGCA]CTGGGATTACAGGCA | 672 |
rs560913479 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125813 | GGGGGTGGAGGGAAA[A/T]AATTATTTCCAGCAT | 672 |
rs560931801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078709 | AGTCTTCAAATGCAT[G/T]ATTTATAGTTTCCTT | 672 |
rs560938838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103736 | TCACTAACTTTTTAT[A/G]TAAATCTATGAGCAT | 672 |
rs561011887 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096442 | CCGGGCGTGGTGGTG[C/T]ATACCTGTAGTCCCA | 672 |
rs561027686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057562 | AAAATTAGGCCGGGT[G/T]TGGTGGCTCACGCCT | 672 |
rs561068913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070515 | AGAGAAATGCTACTA[C/T]CTGGCAGTACATTTG | 672 |
rs561130422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072157 | CTTTGGGAGGCCAAG[A/G]TGGGCGGATCACCTG | 672 |
rs561139858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069632 | TTGCTGGTCTGGACA[C/T]GGGATTATGAGATGA | 672 |
rs561146481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063440 | TTTCACGGAGATAGA[A/G]AGGTCAGCGATTCAC | 672 |
rs561152946 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127012 | AGCACTGCCGGCCCG[C/T]CTGCACCCCGCTTGA | 672 |
rs561256666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120601 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAAAAT | 672 |
rs561269443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065077 | CCTCGTGATCTGCCC[A/G]CCTTGGCCCCCCAAA | 672 |
rs561326470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114220 | TTATGGGCAGGAGCT[A/G]CCACACTGGGCCCTT | 672 |
rs561369681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058260 | GTGCCTGCAGTCCCA[A/G]TTTCTTGAAAAGCTG | 672 |
rs561370557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121301 | AATGGCCTGAACCCG[A/G]GAGGCGGAGCTGGCA | 672 |
rs561391153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113673 | CGCCCGTCCTCTATT[C/T]TCTTTTATTTGTACA | 672 |
rs561395866 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077981 | CTCAGGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 672 |
rs561414242 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065832 | TGAGTGAGTCTTAAT[C/T]CTGTTCCAGATAACA | 672 |
rs561655234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079567 | TGCCAAGAGAATTAA[C/T]GTGCGTATTGAGCAC | 672 |
rs561670417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077071 | GACTGTATGAAATGG[G/T]GATTTCAGCTTCTGC | 672 |
rs561683778 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077896 | ATGCACCACCTCGCC[C/T]AACTAATTTTGTATT | 672 |
rs561706745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045881 | AATCGACTCCAGGGT[C/T]CTGGTTGTATGAGTT | 672 |
rs561728699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075995 | CTACTCAGGAGGCTA[A/G]GGTGGGAGGATTGCT | 672 |
rs561737049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095237 | CAGACTTACCACTCC[C/G]TATATTTAAAAACCA | 672 |
rs561790910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117079 | CACTTCAGAAGAGGC[A/G]TGATGTTTGGTTTGT | 672 |
rs561815103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087991 | TCCGGGGCTCAGGCA[A/G]TCTTCCTGCCTCACC | 672 |
rs561853157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100928 | GTAGAGACAGGTTTC[G/T]CCATGTTGGCCAGGC | 672 |
rs561876983 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087235 | TATCAGGATGCCACT[A/T]TAGTGATGTACATAA | 672 |
rs561954959 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045023 | TGGCCAGGCTGGTTT[C/T]GAACTCCTGACCTCC | 672 |
rs561974843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048242 | GAGTCTCGCTCTGTC[A/G]CCCGGGCTGGAGTGC | 672 |
rs561985161 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084628 | AAGCCATCTTCTTTC[C/T]CCTGCTACACTGAGT | 672 |
rs561988641 | snp | C/T | 8.23988e-05 | 0.00641815 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093526 | GTTCTTTACCTTCCA[C/T]GAGTTGTAGGTTTCT | 672 |
rs561998108 | snp | C/G/T | 3.29506e-05 | 0.00405884 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43094608 | AAGCCAGGCTGTTTG[C/G/T]TTTTATTACAGAATT | 672 |
rs562031586 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111545 | AAAAAAAAACAGCCG[A/G]GCGTGGTGGCTCACA | 672 |
rs562072846 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077175 | TTACCGAAAAAAAAG[-/A]AAAAAAACAAATAAA | 672 |
rs562100327 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086393 | AAAACAAACAAAAAC[C/T]CAGATATCAATGATA | 672 |
rs562162183 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116287 | ATAAAATGAACTATA[G/T]GGACCATCACCCTGG | 672 |
rs562197830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102845 | CTTTTAATATAGACA[A/T]GGACTTGCTATGTTG | 672 |
rs562207926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079123 | ACATTGTAATGAGCC[G/T]AAATCACACCATTGC | 672 |
rs562222209 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123093 | AAAATTAGCTGGGCA[C/T]GGTGGTGCACACCTA | 672 |
rs562250383 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050765 | TTACCTATCCAAAGA[C/T]ATTTTCTCACTAACA | 672 |
rs562254980 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048289 | CTCACTGCAACCTCC[A/G]CCTCCGGGGTTCAAG | 672 |
rs562269090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053874 | CTTAGGAGGCTGAGG[A/C]AGGAGAATCACTTGA | 672 |
rs562284966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109925 | TTTTAGACGGAGTCT[C/T]GCTCTGTCTCTCAGG | 672 |
rs562302203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069404 | GCTTGTTTAAAGACA[A/G]CATGTACCCAAGCCA | 672 |
rs562306899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117621 | GCATGCGCCTGTAAT[C/T]CCAGCTACTTGGGAG | 672 |
rs562368660 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120629 | AATTAGCCGGGCGTG[A/G]TGGTGGACGCCTGTA | 672 |
rs562370358 | snp | A/G/T | 1.64795e-05 | 0.00287045 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093183 | ACTTCCAGTAACGAG[A/G/T]TACTTTCCTGAGTGC | 672 |
rs562403569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047448 | CTTACTCCCACCCCA[C/T]GGAAACAGTTCATGT | 672 |
rs562419872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102288 | ATGTGAGCCAGGATA[C/G]TCTTGATCTCCACAC | 672 |
rs562491188 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067198 | CATAAAGTAATTGAT[A/T]GACTATTAGAAGACT | 672 |
rs562525841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110875 | GGAGGCTGAGGTGGG[C/T]GGATCACCTGAGGTC | 672 |
rs562553169 | snp | C/G | 1.6486e-05 | 0.00287102 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094360 | CAGAACCTAACAGTT[C/G]ATCACTTCTGGAAAA | 672 |
rs562562021 | in-del | -/AC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052780 | GACAGACGGACAGAA[-/AC]ACACACACACACACA | 672 |
rs562568020 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113663 | TGAGCCACCGCGCCC[A/G]TCCTCTATTTTCTTT | 672 |
rs562625234 | snp | A/G | 5.53807e-05 | 0.00526187 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43079318 | TGACGAACACAAAGG[A/G]AAAGAGGAGAGGCAC | 672 |
rs562679568 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084762 | TGCCATTGCCACCAC[A/G]TGGTACTCGTGAGTA | 672 |
rs562815577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085741 | GCAGAATGTGGCTAA[C/T]TCTAATAAGACTCCT | 672 |
rs562842179 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105795 | TCTCATAGAATTTAC[A/G]TTGTAGCAGAAGAGA | 672 |
rs562848044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048940 | CCCTCAGTATATTTA[A/G]TATGTGCAGTTCTCA | 672 |
rs562927690 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077135 | ATGAAAGAAAAAACA[A/G]GTGACATTTTGCTTC | 672 |
rs562962474 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048241 | GGAGTCTCGCTCTGT[C/T]GCCCGGGCTGGAGTG | 672 |
rs562983410 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070680 | GTCCTATATCATACC[A/C]AAAGTATAGCTTTTC | 672 |
rs563014819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095761 | TTGTAAAGGTCCCAA[A/G]TGGTCTTCAGAATAA | 672 |
rs563017140 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125840 | GCATGCGTTGCGGAA[C/T]GAAAGGTCTTCGCCA | 672 |
rs563091836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102967 | TTTTTTTTTTTAATT[A/G]CAGAGACAGTGTCTC | 672 |
rs563228641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095356 | GGAGGCTGAAGTGGG[C/T]AGACTGCTTGAGTCC | 672 |
rs563470320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098734 | GCTGGTCTTAAACTC[A/G]TGGACTCAACCAATC | 672 |
rs563493286 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045116 | GGTTTCAAGTTTCCT[C/T]TTCATTTCTAATACC | 672 |
rs563531357 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100338 | AATCACATCTGATAA[A/C]TTTTTTTTTTGTTTT | 672 |
rs563690868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060507 | TATCATTATTATTTC[C/T]TGAGACAGGAGTCTT | 672 |
rs563797962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045962 | GAGTCTTGCTCTGTC[A/G]CCGAGGCTAGAGTGT | 672 |
rs563825584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075821 | TAAATACACATCTCT[C/G]AAAGATATTCTAAAT | 672 |
rs563886788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074782 | GGTCAGTAGCTGGGT[A/G]TGGTGGCTGGCGCCT | 672 |
rs563952039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060092 | TTTTTGTTTTTGAGA[C/T]GGAGTTTCACTCTTG | 672 |
rs563979083 | in-del | -/ATC | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119771 | AAATTGGATTCAGTT[-/ATC]ATACCAGATGGCTTT | 672 |
rs564004787 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124337 | TTCACATATTGCTGC[C/T]AACCCCTTGGGTCTT | 672 |
rs564043252 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044942 | CTGAGTAGCTGGGAT[A/T]ACAGGTGTCCACCAC | 672 |
rs564046610 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43123419 | TCAGTGGTGCCATAT[G/T]GGCTCACAGCAACAT | 672 |
rs564119849 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083874 | TTATTTTATTTATTT[A/T]TTTTTTTTGAGACAG | 672 |
rs564249425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116071 | AGTTGATAATAGTTC[A/G]TACGAATTCATTTCC | 672 |
rs564259164 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051795 | GCGCGCACCACCACG[C/T]CCGGCTAATTTTTGT | 672 |
rs564269997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099384 | CAAGTGATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 672 |
rs564288136 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079462 | AAAAAGGAATGCCCC[A/T]CAAGTGTTACCATGG | 672 |
rs564362551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067551 | GCGCCACCGTGCCTC[A/G]CCTCATGTGGTTTTA | 672 |
rs564375670 | snp | G/T | 1.64803e-05 | 0.00287052 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093018 | GTTTCCCGACTGTGG[G/T]TAACTTCATGTCCCA | 672 |
rs564392397 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101265 | GTGGTGGCGTGATCT[C/T]GGTTCACTGCAACCT | 672 |
rs564394281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109868 | AGTGGAACTAGATAC[A/G]CAAAAATCAACCAAG | 672 |
rs564407408 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099996 | CATCAGTCAGCTAAC[A/C]TGTATGATGCCTGGA | 672 |
rs564438587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047125 | TTCTTTTTGAGACAC[A/G]GTCTCGCTCTGTCGC | 672 |
rs564472502 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051327 | TTTCAGAAGATCTTC[C/T]TGAAGTGCATATGTA | 672 |
rs564536706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105300 | GCTAGCATGCAGTGC[C/T]ACAATCATAGCTCAC | 672 |
rs564566924 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116482 | GCAATCCTCCCAGCA[C/T]GGGGTTTACAGGCAT | 672 |
rs564682165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117056 | GGTACTGTGTACTCT[C/T]ATTAGATCACTTCAG | 672 |
rs564757581 | snp | A/C | 1.67105e-05 | 0.0028905 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43071235 | TCCAGGTAAGGGGTT[A/C]CCTCTGAAAGGAATG | 672 |
rs564791752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053048 | CACCCGGCTAATTTT[C/T]TGTATTTTTAGTAGA | 672 |
rs564842903 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050543 | ACTTGAACCCGGGAG[G/T]TGGAGGTTGCAGTGA | 672 |
rs564893258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096760 | CAGTCACAATTACTG[C/T]TGTGTCAATATTACT | 672 |
rs564895974 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058560 | CAGAACTTAACAATC[A/G]GCTTTTCACCTCACT | 672 |
rs564901938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049877 | CCGTTTCTGGGAATT[A/G]CTGAGGTGCTCCTGT | 672 |
rs564924789 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119664 | ATGTGACTTTAAAAA[A/G]AAAAACAACCTTGAC | 672 |
rs564927512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057372 | AAAAATTAGTTGGGC[A/G]TGGTGGCAGGCACCT | 672 |
rs564961882 | in-del | -/AT | 0.000527741 | 0.0162355 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124136 | ACACATTAGAAAAAC[-/AT]ATATATATATCTTTT | 672 |
rs564964039 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126379 | GCCATGTTAGATTCA[C/T]CCCACAGAGATAGCG | 672 |
rs565025391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056719 | AGAGAGAGAGAGAAA[G/T]ACACCCCAGTGAAGT | 672 |
rs565028586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051336 | ATCTTCTTGAAGTGC[A/G]TATGTAGTTGACCTG | 672 |
rs565092405 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060449 | TGCCTCGGCCTCCTA[A/G]AGTGCTGGAATTACA | 672 |
rs565093007 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127082 | TCAGGACCTGCAGCC[C/T]GCCATGCCCGAGCCC | 672 |
rs565097783 | in-del | -/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126918 | GGGCGCGGGCTCAGC[-/G]GGCCCCGCACCCCCG | 672 |
rs565110238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063505 | CTTCCCTCTAAAGCC[A/G]CAGCCCTTTAATAAG | 672 |
rs565116707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114641 | GTGGTTGTCTGGGGA[A/G]GGAACAGGGAGGCAG | 672 |
rs565120256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119075 | GTGAATTTTTGAAAC[A/G]GATTTTTTGGATAAA | 672 |
rs565159136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065957 | TTACTTTTATGTATC[C/T]TTACCATCTACCTCT | 672 |
rs565167448 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121349 | CACTGCACTCCAGCC[G/T]AGGCAGCAGAGCGAG | 672 |
rs565242394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066593 | TTTATGTATTTTTAG[G/T]AGAGACTGGGTTTTA | 672 |
rs565275419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122388 | CTAGGTCCCAAGTAC[C/T]GTTCTAACTACTGAA | 672 |
rs565288543 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126855 | GGAGAGGCGGGTGTG[A/G]GAACTGGGGCTGCGC | 672 |
rs565376783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059186 | TTCATGCATCTGGCC[A/G]GGCACAGTGGCTCAC | 672 |
rs565423930 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127107 | GAGCCCCCTCCCAAC[C/T]CCTGTGAGCTCCAGC | 672 |
rs565436199 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127391 | TAGCTAATCTGGTGG[A/G]CACTTGGAGAACTTC | 672 |
rs565491313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080340 | AGGTGGGATTACAGG[C/T]ATGTGCCACCACGCC | 672 |
rs565506386 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051931 | TAAGCCACTGCGCCC[A/G]GCCCTCTCTGACTTT | 672 |
rs565514357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096304 | ATGGCTTCAACCTGG[A/G]AGGCAGACGTTGCGG | 672 |
rs565516352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104470 | AATACACAGACCATC[A/G]AAGTTATTTAGAGTC | 672 |
rs565564553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073007 | CAGGCATGAGCAGTG[A/G]CTGTAATCTGTCCTT | 672 |
rs565578525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103867 | ATCCCAGCAATTTGG[C/G]GAGCCGAGGTGGGTG | 672 |
rs565651464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096921 | AATGAGAGAACTAAA[C/T]TAGATGATCTCTAAG | 672 |
rs565744507 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072388 | GAGTGAAACTCCGTC[A/T]CAAAAAAGAGTACGG | 672 |
rs565748317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064861 | TTTGAGATGCAGTCT[C/T]GCTCTGTCAGCCAGG | 672 |
rs565786952 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064345 | AATATGTGAAAGAAG[-/A]AAACAGTATTGTTGA | 672 |
rs565787665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089383 | ATATTCATTTTTAGA[C/T]GTTGTGATACAGAAT | 672 |
rs565798527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080487 | CAGGCGTGAGCCACC[A/G]TACCCGGCAACAATA | 672 |
rs565831059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050152 | GACCTAAGTCCCTGG[G/T]CAGAAGCAGGCACAG | 672 |
rs565847516 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072954 | CTCTTGGCCTCGAGC[-/A]AATTCTCCCACCTTG | 672 |
rs565983258 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096751 | ATTTTCATCAGTCAC[-/A]AATTACTGCTGTGTC | 672 |
rs565983370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120938 | CCACGGTGGCGTGCG[C/T]CTATAATCCCAGCTA | 672 |
rs566056815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098939 | TCTCCTGCCTCAGCC[A/T]CCTGAGTAGCTGGGA | 672 |
rs566088735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051468 | TGTTAGATGCAAGGG[A/G]AAAAAGGTCCTTCTG | 672 |
rs566118195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098141 | TGTATCCACTCACCT[C/T]TGCCTCCTGAGTAGC | 672 |
rs566230299 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086042 | AAGCAACTTTGCAAT[A/G]AGTGTTTATATATCT | 672 |
rs566244754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105778 | ACAGACAAAATTACT[A/G]CTCTCATAGAATTTA | 672 |
rs566284161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057873 | AAAAAACCAAAAATT[A/T]GCTGGGCGTGGTGGC | 672 |
rs566363471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114861 | CACTTGTTCTACTAA[A/G]TTACCTACTCTACTT | 672 |
rs566366625 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089492 | TTTTATTTATTTCAT[A/T]GGTGACCAAATTATT | 672 |
rs566370206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054065 | AGTATTTTCAGAATG[C/T]CATTACTTTGACCAC | 672 |
rs566378020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124204 | TTTAAAATAAAGTAA[A/C]TTTAAGATTTGGAAG | 672 |
rs566416929 | in-del | -/GAAAGAAAGGAAAG | 0.0142736 | 0.0832652 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074921 | GCAAGACTCTGTCAA[-/GAAAGAAAGGAAAG]GAAAGAAAGGAAAGA | 672 |
rs566443477 | in-del | -/AAAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072042 | AATAAATAAATAAAT[-/AAAA]GTTTATGTAAAATGA | 672 |
rs566512455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101700 | TAGAGATGGGTTTCA[C/T]CATGTTGGCCAGGCT | 672 |
rs566512705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43086571 | TGCTTAGTAAAAACA[C/T]GTTGCAAAATGAATC | 672 |
rs566529348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062679 | CTTGGCTCATTGCAA[C/T]CTCCACCTCCCGGGT | 672 |
rs566614279 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065101 | CCCCAAAGCGCTGGG[A/T]TTACAGGCCTGAGCC | 672 |
rs566625653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117311 | GCCGGGCGTGGTGGC[A/G]CATGCCTGTGGTCTC | 672 |
rs566672587 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067978 | ACATTTAAAAAATTC[G/T]AAGACACCTGAAGTC | 672 |
rs566705389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117695 | AGTGAGCCAAGATCG[C/T]GCCACTGTACTCCAA | 672 |
rs566714275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119113 | CAAGATATCAAAGAA[C/T]GACTAACCTGGCAGT | 672 |
rs566788810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070020 | CTCACCGCAACCTCC[A/G]CCTCCCGGGTTCAAG | 672 |
rs566810396 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097907 | GGGGGAAAACAGTAA[A/G]TGTTATGATAAATAG | 672 |
rs566820747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111379 | ACAAAAATTAGCCAG[A/G]TGTGGTGGCACATGC | 672 |
rs566843392 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100667 | TATAACATATATATA[C/T]ATATATATATAATAT | 672 |
rs566941009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087555 | TAATCCCAGCTACTC[G/T]GGAGGCTGAGGCAGG | 672 |
rs567002905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055008 | ACCCGCCTTGGGCTC[C/T]CAAAGTGCTGGGATC | 672 |
rs567043731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077775 | GTTTGCTCTTGTTGC[A/C]CAGGCTGCAGTGCAA | 672 |
rs567110235 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118386 | CTTTTTAATTTTCTT[G/T]TTTTTTTTCAGACAG | 672 |
rs567157356 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125586 | GAAAGAGACGGAAGA[G/T]GAAGAATTCTACCTG | 672 |
rs567171193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117849 | GATTAGTTCATTTAT[C/T]ATACTAATATAACAA | 672 |
rs567172573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048391 | TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCATGT | 672 |
rs567260091 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059180 | TCAAAATTCATGCAT[C/G]TGGCCGGGCACAGTG | 672 |
rs567279321 | snp | C/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127449 | ACCAATCAGTGCTCT[C/G]TGTCTAGCTCAAGGT | 672 |
rs567340802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088499 | TGTCCTTTGGTGTCC[A/G]GTTTATTTCAGTTAA | 672 |
rs567491387 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064979 | GGGACTACAGATGCC[C/T]GCCACCATGCCCGGC | 672 |
rs567534295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048090 | TTGTAGACATGAGGT[C/T]CTACTGTATTGCCCA | 672 |
rs567549846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054734 | AAGTGAGCCGCTGTG[C/T]CCAGCTGGGATTTTT | 672 |
rs567552388 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095603 | AACAAACAAACAAAC[-/A]AAAAAAAAAAACGAA | 672 |
rs567615618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097103 | CCCAAGTCGTGTGTT[C/T]ACCTATATAACAAAC | 672 |
rs567636286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050236 | ACACCAAGGCCTTTG[C/T]GCTGCGCAACTCCAG | 672 |
rs567683345 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061710 | GCCTCAGCCTCCCCA[A/G/T]CAGCTAGGATTACAG | 672 |
rs567691685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119943 | AAGACTGTGAAAAGG[A/G]AAAAGAAAAAAAATT | 672 |
rs567710149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111903 | GCTTGCTTGGGTCAA[G/T]AAAGTTGTTTTATTT | 672 |
rs567771938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079015 | GACCAGCCCGGCCAA[C/T]ATGGTGAAACCCTGT | 672 |
rs567832326 | in-del | -/AGG | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083828 | GAATTTAGGTATGTA[-/AGG]AGTTTTCCAAAATAT | 672 |
rs567951277 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107537 | AGACATGCACCACCA[C/T]ACCCAGCTAATTTTT | 672 |
rs567975560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119264 | GGTGACAGAGAATCC[A/C]TCTCAAAAAAAGAAA | 672 |
rs567980544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066880 | TGGAGTGCAATGGTG[C/T]GATCTTGGGTCACTG | 672 |
rs568050020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116588 | CAATGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 672 |
rs568088681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123561 | CACCATGTTGGCCAG[A/G]ATGGTCTCGATCTCC | 672 |
rs568108675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100563 | GTGTGTGTGTGTATA[C/T]ATATATATAACATAT | 672 |
rs568111260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115932 | TTTATTAAATGTCTG[C/T]TGTGTCAGGAACTGA | 672 |
rs568154063 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43073665 | CTTTGGGATTTGACT[A/C]ATTTTCTAATAAAGG | 672 |
rs568225296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117471 | ATAAGGCCAGACACG[A/G]GGGCTCATGCTTGTA | 672 |
rs568238249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082988 | TCATCAGACATTTAG[G/T]TTAGTTCATATAAAA | 672 |
rs568312345 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093391 | TAAGTTCACTGGTAT[C/T]TGAACACTTAGTAAA | 672 |
rs568366440 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045013 | TTCACCATGTTGGCC[A/G]GGCTGGTTTCGAACT | 672 |
rs568367097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085148 | TGCTCTGATCTCTAC[C/T]TTTAATACAGCTACA | 672 |
rs568374156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074172 | TCAAGTAAACCTTGA[A/T]TAACACTTGAGCTAT | 672 |
rs568392972 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072330 | GGAGGCGGAGGTTGC[A/G]CTGAGCCGAGATTGC | 672 |
rs568430563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068829 | GCGATCAATTCTCTC[A/G]TAAGAAGGCTTAGAA | 672 |
rs568448767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084298 | GCCTCCCAAAGTGCT[C/G]GGATTACAGGCGTGA | 672 |
rs568459377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103828 | AATGGTTTTACCGGC[C/T]GGGCACAGTGGCTCA | 672 |
rs568469132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053380 | GAAATTTGAAGTTTC[A/G]GGCTTGGCGTAGTGG | 672 |
rs568477212 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110346 | AATCCTAGCACTTTG[A/G]GATGCCTAGGTGGGC | 672 |
rs568489462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077477 | CTGACATTACAGGTG[C/G]CTGCCACCACGCCCA | 672 |
rs568538427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101564 | CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCGCT | 672 |
rs568570401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068048 | TTTGGGAGGCTGAGG[C/T]GGGCAGATCACAAGG | 672 |
rs568583007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053190 | GTGCCACTCTCACTA[C/T]CTGTATGAATAAACC | 672 |
rs568599423 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109217 | GCCCAGTCTGGTCTC[A/G]AACTCCTGACCTCAA | 672 |
rs568603740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43046449 | GTCACTCAGGCTGGA[C/T]TGTGATGGTGTGATC | 672 |
rs568652972 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065167 | TGATGCAAACCTATA[A/G]CTTAAGGTATCTTAA | 672 |
rs568752548 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110132 | ATCTCCTGACCTCGT[C/G]ATGTGCCCATCTCAG | 672 |
rs568753972 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071215 | AGAAGAGGCTGATTC[C/T]AGATTCCAGGTAAGG | 672 |
rs568916281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108522 | AGCCTGGCTAACATG[A/G]TGAAACCCTGTCTCT | 672 |
rs568955934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43101643 | GAGTAGCTGGGATTA[C/T]AGGTACGTGCCACCA | 672 |
rs569040435 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067802 | TGTAGCAATCCTGCA[C/T]GTTCTACACGTGTCC | 672 |
rs569074958 | snp | C/T | 1.76767e-05 | 0.00297289 | splice-acceptor-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124116 | TTCTGTTCCAATGAA[C/T]TTTAACACATTAGAA | 672 |
rs569080428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074908 | CCTGAGTGACAGAGC[A/G]AGACTCTGTCAAGAA | 672 |
rs569113962 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125449 | CAAGGGGCTACCGCT[A/G]AGCAGCAGCCTCTCA | 672 |
rs569117428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060222 | GGGATTAGAGGCACG[C/T]GCCACCACGCTGGGC | 672 |
rs569138982 | snp | C/T | 4.94181e-05 | 0.00497057 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047599 | GATAAACCAAACCCA[C/T]GCAAAAGGACCCCAT | 672 |
rs569170973 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071755 | ACACCTGTAATCCCA[C/G]CACTTTGGGAGGCCG | 672 |
rs569183763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43077669 | TTACTCCTCCAAATG[A/T]ATCACTTTGTGCCAC | 672 |
rs569197348 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104679 | ATGTGAAAAATGTGC[A/G]CCTTACGATTGATAA | 672 |
rs569208003 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068209 | GTGAACCCAGGAAGC[A/C]GAGCTTGCAGTAAGC | 672 |
rs569210863 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101224 | TTTTTTTAGACAGAG[C/T]CTTGTTCTGTTGCCC | 672 |
rs569237216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062621 | TTTTTTTTTTTAAGA[C/T]GGAGTCTCGCTCTGT | 672 |
rs569264312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120948 | GTGCGCCTATAATCC[C/T]AGCTACTCAGGAGGC | 672 |
rs569300149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069825 | AATAAAGATATTTCA[A/G]AATGACTTGGTCATC | 672 |
rs569319683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081634 | CATCTCCTATGTGTC[C/T]GTTTGTTTGCCCCTA | 672 |
rs569407328 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109638 | AAAACTCAGAATAGA[A/G]GCTCCCACTCCTTCA | 672 |
rs569427551 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126985 | AGCTGCAGAGGGTGC[A/G]CCGGGTCCCCCAGCA | 672 |
rs569446512 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113271 | TGGACCTTCTCTTTC[C/T]TGCAAATGGCTTCCC | 672 |
rs569556577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072658 | AAACCTCTGCCTCCC[A/T]GGTTCAAGCGATTCT | 672 |
rs569593353 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127170 | CTGCTCCTCAGCGCC[C/T]GGTCCCATCGACTGC | 672 |
rs569714478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066259 | TAAAAGAGAAAGGTA[C/T]AGGACAAATGATCTG | 672 |
rs569721756 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077954 | TGGTCACGCTGGTCT[C/T]GAACTCCCGACCTCA | 672 |
rs569749280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121448 | CCAGCACTTTCGGAG[A/G]CCAAGGCAGGAGGAT | 672 |
rs569802083 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046301 | AATGGCACGATCTCA[C/G]CTCACTGCAACCTCC | 672 |
rs569832880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097802 | ACAAGAAAAGCACAA[C/T]AGTGCCTGGAATATA | 672 |
rs570062354 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044394 | CCCTTGCACACTGGG[A/G]GGGCTAGGGAAGACC | 672 |
rs570133122 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084175 | AGCTGGGATTACAGG[C/T]GCCCGCCACCATGCC | 672 |
rs570133578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106574 | CAATTTAATTTACTT[C/T]CTTTTGTAGAAAGAA | 672 |
rs570200697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43083079 | AAAATACAACAAATA[C/T]AAAAATACTATCAGT | 672 |
rs570207518 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052046 | AATCTAGAAGTGAAG[C/G]CAGGTTCTGCCTCTC | 672 |
rs570221030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059411 | GAGGTTGGAGTGAGC[C/T]GAGATCGTGCTACCG | 672 |
rs570271499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099098 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACTG | 672 |
rs570282743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058666 | ATACTGTGCTGTTAT[A/G]AAGGTAACTGAAAAA | 672 |
rs570303581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080745 | GGAGGTCGAGAGGCT[G/T]CAGTGAGCTGTGATT | 672 |
rs570318461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115162 | TGCTTTCACTGATGG[A/G]CACAAAAAATACAAA | 672 |
rs570357989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051870 | TCGAACTCCTGACCT[C/T]GTGATCTGCCTGTCT | 672 |
rs570399137 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121576 | CAATCCCAGGTACTC[A/C/T]GGAGGCTGAGGCAGC | 672 |
rs570502555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058822 | AGTTAGAGGTTTTTC[A/T]TAATTACTATTATGA | 672 |
rs570513790 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059513 | CAACAACAACAACAA[A/C]AAATTCTCACATCTA | 672 |
rs570578083 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072718 | TACAGGCATAAGCCA[C/T]CAAGCCTGGCTAATT | 672 |
rs570691191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108270 | TTGAACCTGTGAGGC[A/G]GGGGTTACAGTGAGC | 672 |
rs570693264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099688 | TGCCTACCACAAATA[C/T]AAATTATGACCAAGA | 672 |
rs570787991 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43045973 | TGTCGCCGAGGCTAG[A/G]GTGTGATGGCGCAAT | 672 |
rs570828029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100526 | TGTGTGTGTGTGTGT[A/G]TATATATATACATAT | 672 |
rs570830035 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102823 | ATGCCCAGATAATTT[A/T]AAAAAACTTTTAATA | 672 |
rs570862095 | in-del | -/CTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090061 | AAAGGGAAAAAAAAA[-/CTT]AAGAAGAGAAAGAAG | 672 |
rs570884346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084974 | ATAACTTTCCTTTGG[C/G]TTTCCCAAAGGAATT | 672 |
rs570920520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067406 | ACTACAGGCGCACGC[A/G]ACCACACCCAGCTAA | 672 |
rs570921049 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052726 | GAAGCTAAAAATACA[C/T]GGATGGCCTTTTAGA | 672 |
rs570924244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076283 | ACATATCTATCTAAC[C/T]GCACATTTCTCATGT | 672 |
rs570980705 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090597 | CCAGGCTGGTCTCAA[A/C]CTTCTGACCTGAGGT | 672 |
rs570987062 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067826 | CGTGTCCTGGAACTA[C/T]TTAAAGTGAATTTTT | 672 |
rs571007748 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044561 | GAAAGCAACAGCTTC[C/T]TTCCTGGTGGGATCT | 672 |
rs571088594 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103188 | GCTCTCTTTTTTGGC[C/T]GGGCTTGGTGGCTCA | 672 |
rs571090664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111780 | TGAGCCGAGACTGCA[C/T]CACCGCACTCCAGCC | 672 |
rs571095658 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117939 | AGTTTACAAAATAAA[A/G]CCTGCTCTCATAGAG | 672 |
rs571123613 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114131 | GGAGTGCAGTGGTGT[C/G]ATCATAGCTCACTAC | 672 |
rs571130383 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080814 | CTCTCTATAAGGTGA[-/G]GCTCAGGTCGGGGAG | 672 |
rs571148033 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045250 | ATTGAAGGGTCTGAC[C/T]CTCTGCCTTTGTGAA | 672 |
rs571152998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088665 | ATAAAAAAACATCAT[C/T]CACTTACTAGCAGCT | 672 |
rs571308646 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084252 | AGCCAGGATGGTCTG[C/G]ATCTCCTGACCACAT | 672 |
rs571319167 | in-del | -/T | 0.26078 | 0.249767 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084032 | ACCATGCCCGACTAA[-/T]TTTTTTTTTTTTTTT | 672 |
rs571402533 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079095 | ATCCCAGCTACCCAG[A/G]AGGCTGAGGCGGACA | 672 |
rs571406044 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125788 | AAATATAAGTAATAA[A/G]GATTGTTGGGGGGGT | 672 |
rs571419990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048495 | CAGGCGTGAGCCACC[A/G]CACCTAGCTTTTCTC | 672 |
rs571420294 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056212 | AGATCTTCTGTCTGT[C/T]GTCTAGGCTGGAGTG | 672 |
rs571445368 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097593 | CCCCCGTTTCTACTG[-/A]AAACAAAAACAAAAA | 672 |
rs571605026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090742 | GTAGGCTGTGTGTGC[A/G]CGTGTGCGTGTGTGT | 672 |
rs571659138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119520 | TCACCCTGCCAGACT[C/T]CTTGGGCTATTGCAA | 672 |
rs571661474 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075626 | GGAGTGCAATGGCAC[A/G]GTCCCAGCTCACTGC | 672 |
rs571666267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097983 | TAAATATATTCTAAA[A/G]GAAAATCCAATTTGA | 672 |
rs571706912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120123 | GCAGCTAGGTTTAGG[C/T]TGAAAAACAACAACC | 672 |
rs571713225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104722 | GACCAGTGGGAGTAA[G/T]TTTTTAAAAATAGAT | 672 |
rs571724444 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060025 | ATTCTCCTGCCCCAG[C/T]CTCCCAAGTAGCTGT | 672 |
rs571745729 | snp | C/G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126251 | GCTTTTGCCCCGTCT[C/G/T]CGTCGACGCAATCGC | 672 |
rs571747626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119018 | TGATCCATCTGCCTC[A/G]ACCGGGATTACAGGC | 672 |
rs571793842 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126737 | TGGCGTCCATTCTGG[C/T]CGTGCTGGAGGAGCC | 672 |
rs571821518 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43061422 | TCGACAGAACCTGAA[C/T]CCTACCAGGGACTTA | 672 |
rs571834423 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057061 | CTTTACCTTTCTGTC[C/T]TGGGATTCTCTTGCT | 672 |
rs571879954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071544 | TAATTTTAGAAACAA[C/T]GTAGTTGTCCAATAA | 672 |
rs571895485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064722 | ACTGCTACAAAAGCC[A/G]ATTTAGTAACATTTA | 672 |
rs571927660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120830 | CCAGCACTTTGGAAG[G/T]CCGAGGCGGGTGGAT | 672 |
rs571949438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095689 | TTAAATCTATCAGAC[C/T]ATACCACGACATTTG | 672 |
rs571973705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112860 | CCAGGCTGGAGTGCA[A/G]TGGCGCAATCTCGGC | 672 |
rs572017299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43056579 | AGGATCACAAGGTCA[A/G]GGGTTCAAGACCAGC | 672 |
rs572056940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112185 | GCCTCTGCCTCCTGG[A/G]TTCAAGAGGTTCCTC | 672 |
rs572127645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087944 | CAGAACAGAGTGCAG[C/T]AGCGTGATCACAACT | 672 |
rs572246707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43087074 | GTACAGGAAAATGGG[A/C]ACTATCATATACCAC | 672 |
rs572261027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079135 | GCCGAAATCACACCA[C/T]TGCACTCCAGCCTGG | 672 |
rs572266836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078661 | TAAGACACTGGGTAG[C/G]CTGGGGGGAAATAAT | 672 |
rs572345927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43080240 | CTAAGCATTGTACAG[A/G]GTATTGTGAAGAATT | 672 |
rs572438182 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126975 | CCGGGCCAGCAGCTG[C/T]AGAGGGTGCGCCGGG | 672 |
rs572457502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072934 | ATTGCCCAGGCTGGT[C/G]TTGAACTCTTGGCCT | 672 |
rs572479974 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118751 | CTTTAGCTTTCTTCT[A/C/G]AATGTGAACCTTTTT | 672 |
rs572481230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072047 | ATAAATAAATAAAAG[C/T]TTATGTAAAATGACT | 672 |
rs572548765 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127365 | GGATGCACCAATCAG[C/T]ACTCTGTATCTAGCT | 672 |
rs572585822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105072 | CAGCAACAGTAGAAA[A/G]CCTCTATAATCAATA | 672 |
rs572604463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057229 | ATTTAAGGCATTCAG[G/T]CCAGGCGCAGTGGCT | 672 |
rs572649808 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43112953 | GGATTACAGGCATGC[A/G]CCTCCACGCCCGTCT | 672 |
rs572736614 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089934 | ATCGCTTGAGCCCAG[A/G]AAGTCAAAGCTACAG | 672 |
rs572745495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43050394 | CGGGTGGATCACGAG[A/G]TCAGGAGATCGGGAC | 672 |
rs572766355 | in-del | -/GGAGTGGAATAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056992 | CCATCTCTGCAAAGG[-/GGAGTGGAATAC]GGAGTGGAATACAGA | 672 |
rs572778206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084619 | ACTAAAAACAAGCCA[C/T]CTTCTTTCTCCTGCT | 672 |
rs572811515 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121491 | GGAGTTCGAGACCAA[-/C]CTGACCAATATGGAG | 672 |
rs572835027 | snp | C/T | 3.29576e-05 | 0.00405928 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093494 | TGGCTTGTTACTCTT[C/T]TTGGCTCCAGTTGCA | 672 |
rs572848769 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044964 | GTCCACCACCATGAC[C/T]GGCTAATTTCTGTAT | 672 |
rs572870197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43085548 | CACAAGTTGTTTTCC[G/T]ATAACACATGACAAC | 672 |
rs572878542 | in-del | -/TTTTG | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124748 | ATACCAGCCGGTGTT[-/TTTTG]TTTTGTTTTGTTTTG | 672 |
rs572916676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108806 | AAGACCAGCCTGACC[A/G]ACACGGAGAAACCCT | 672 |
rs572954469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060335 | GAATGAGCCACCACA[C/T]CCAGCCGTGCCCAGC | 672 |
rs572963929 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075602 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 672 |
rs572999365 | in-del | -/TGTT | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081634 | CATCTCCTATGTGTC[-/TGTT]TGTTTGCCCCTATTT | 672 |
rs573003316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103325 | TACAAAAATTAGCCA[A/G]GTCTGGTGTCGTACC | 672 |
rs573003822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43052234 | TAGTTATTGAGCACT[A/G]GAGATGTGGTTAGGG | 672 |
rs573032148 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126049 | ATACGTACAACTCTT[C/T]AGGGAGACTACAATT | 672 |
rs573039628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100050 | CTAAAATGTCTGGGG[C/T]TGGGAGCGGTAGCTC | 672 |
rs573076649 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119423 | TAAGTCAGGAGGCTG[A/G]GTTTCTACTACCAGT | 672 |
rs573093235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068283 | CTCCGTCTCAAAAAA[A/T]AAAAAAAGATACCTG | 672 |
rs573100611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107848 | GATGATAATTAAAAG[C/T]AGCGATTCACTCATA | 672 |
rs573165701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061852 | GGCCACTCAAAGTGC[G/T]GGGATTATAGGCATG | 672 |
rs573166177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054524 | GGCTCACTGCAGCCT[C/T]GACCTCCCAGACTCA | 672 |
rs573171146 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055040 | CAGGTGTGAGCCACC[A/G]CGACCAGCCTGGGAT | 672 |
rs573175244 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100755 | TTTTTTTTTTTGAGA[A/C]AGAATCTTGCTCTGT | 672 |
rs573182674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110520 | GAGCCTAGGAGGTCA[A/G]GGCAACAGTAAGCCT | 672 |
rs573241959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108442 | TTGGCCGGGTGCAGT[A/G]GCTCATGTCTGCAAT | 672 |
rs573272885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048696 | CTTTTTGTTTTTTTT[A/T]TTTTAGTACAGATGG | 672 |
rs573423630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048217 | TCTCTCTCTCTTTTT[C/T]TTTGAGACGGAGTCT | 672 |
rs573450142 | snp | C/T | 0.00111421 | 0.0235767 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125137 | CCAGGGTTCACAACG[C/T]CTTACGCCTCTCAGG | 672 |
rs573454901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053829 | ACAAAATCAGCTGGG[C/T]GTGGTGGCACATGCC | 672 |
rs573493155 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109898 | GATAAGGATTCGAAT[C/G]TTTTTTTTTTTTTTT | 672 |
rs573514669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124513 | GCCTCCCCGCCCCTA[A/G]CCTTTCCCAGTGACC | 672 |
rs573541495 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120491 | AATCTTAAGGCCGGG[A/C]GCGGTGGCTCACGCC | 672 |
rs573563977 | in-del | -/TTTTG | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124747 | ATACCAGCCGGTGTT[-/TTTTG]TTTTGTTTTGTTTTG | 672 |
rs573603647 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110703 | TTACAGGCTGGGTGC[A/G]GTGGCTCATGCCTAT | 672 |
rs573626625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43069312 | CAGAATTAATCATGT[A/G]TAATACAGTCAGTAG | 672 |
rs573646215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124568 | AAGCACATCCCTGCC[A/G]GCAGCATCTGTTACT | 672 |
rs573691487 | in-del | -/ACATGAATG | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082209 | GGTACTCAGATGACA[-/ACATGAATG]ACTGCCTTGGGTCCC | 672 |
rs573753443 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088875 | GTGTATTCTGCATAG[A/G]ACCCTGTGCTGGGAA | 672 |
rs573759243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078751 | TTTCTGGACCTGTGA[A/G]TTTCTAGGATTGTTA | 672 |
rs573786749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045886 | ACTCCAGGGTCCTGG[G/T]TGTATGAGTTCTTAG | 672 |
rs573801537 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43109543 | CTTCAAGTACCATAT[G/T]GCACTCAACAAAACA | 672 |
rs573829205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100948 | GTTGGCCAGGCTGGT[C/T]TCACACTCCTGACCT | 672 |
rs573888561 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43053691 | AAGAAATTTGAAGTT[G/T]CAGGCCGGGCGCGGT | 672 |
rs573904407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061911 | TTTCACATTTCATTT[G/T]GCCTGATCTGTTGTC | 672 |
rs573905924 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057763 | ATGGCGTGAACCCGG[A/G]AGGCGGAGCTTGCAG | 672 |
rs573933693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049373 | ATTTTAAGTCAATTT[G/T]CCACTGATATGCCAT | 672 |
rs573961690 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103976 | GCCTGGCATGGTGGC[A/G]CGTGCCTGTAATCCC | 672 |
rs573970310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048885 | CACAGAGAGGAGGGG[A/G]AGGGACATATGGGAA | 672 |
rs573975600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43055053 | CCGCGACCAGCCTGG[A/G]ATGTTCTGAAATGCC | 672 |
rs573994644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103399 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 672 |
rs574008372 | snp | A/G | 4.94882e-05 | 0.0049741 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094294 | CATTTAGAACGTCCA[A/G]TACATCAGCTACTTT | 672 |
rs574070797 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060133 | TGGAGTGCAATGGTG[C/T]GATCTCAGCTCACCA | 672 |
rs574081834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099242 | CAAAACATATTTACA[A/C]ATATTTAAAACCAGA | 672 |
rs574184046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070174 | CTGACCTTAGGTGAT[C/T]TGACCACCTCAGCCT | 672 |
rs574255756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048245 | TCTCGCTCTGTCGCC[C/T]GGGCTGGAGTGCAGT | 672 |
rs574256555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43118827 | GGAGTGCAGTGGTGT[C/G]GTCTTGGCTCACTGC | 672 |
rs574256604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110723 | CTCATGCCTATAATC[C/T]CACCATTTTGGGAGG | 672 |
rs574263814 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124891 | CCTCCTGAGTAGCTG[A/G]AGCGGCACCACGCCC | 672 |
rs574285625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065790 | CTTCTGCGTCCTCCA[C/T]GCACTCGTCTGCTTT | 672 |
rs574357822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058899 | TTGAGGAAGAACGCT[C/T]AGAAACAATTCTGAC | 672 |
rs574396059 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111544 | CAAAAAAAAACAGCC[A/G]GGCGTGGTGGCTCAC | 672 |
rs574422664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066356 | GAAAAACTCTCAACA[A/G]TACTCAAACTAGGTG | 672 |
rs574464034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116963 | GTTTAACTTGTTCCT[C/G]TAGCCTTATTTCCTA | 672 |
rs574518856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43114103 | GACAGGGTCTCACTC[C/T]GTCATCTAGGCTGGA | 672 |
rs574601832 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099277 | CTTTCTTTTGCTCTC[-/T]TTTTTTTTTTTAGAT | 672 |
rs574614687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051235 | GAAGAGCTTTTCTTT[C/T]TCTTCTGTTCACCAC | 672 |
rs574636501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43121994 | CAAAAGCAGTTTTTT[C/T]CTACAATGTCATTTC | 672 |
rs574655080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106085 | GATCACGCCACTGCA[C/T]TCCAGCCTCAGTGAC | 672 |
rs574686445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115427 | GAATCGCTTGAACTC[A/G]GGGGGCGGAGGTTGC | 672 |
rs574731550 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103460 | CGACAGAGCGAGACT[C/G]TGTCTCAAAAAAAAA | 672 |
rs574770591 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108073 | ACTAGGGCTGTGCAC[A/G]GTGGTCCACACCTGT | 672 |
rs574853091 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046203 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCT | 672 |
rs574913562 | in-del | -/TGT | 0.0225045 | 0.103662 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100689 | TATAATATATATATA[-/TGT]TATATATATATATGT | 672 |
rs574932997 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106713 | GGATGCTGCATAAGC[-/A]AAAACCTAAACTACA | 672 |
rs574954673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43084411 | CCTCAGGTGATCTGC[C/T]CGCCTCGGCCTCCCA | 672 |
rs575106898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059087 | TCCCATGTTCATAGT[A/C]CTCCTTGTACCCCTG | 672 |
rs575161617 | in-del | -/AAGAAAGGA | 0.00279162 | 0.0372561 | intron-variant | BRCA1 | GRCh38.p7 | 17:43075000 | GGAAGGAAAGAAAGG[-/AAGAAAGGA]AAGAAAGGAAAGAAA | 672 |
rs575360173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43066964 | CTGGGATTACAGGTG[C/T]CTGCCACCACGCCCA | 672 |
rs575394096 | snp | G/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126163 | GGGCAGGGGAAATGC[G/T]CTCTGGCCCATGTCT | 672 |
rs575489354 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43062893 | TGAGCCACTGCACCC[A/G]ATTTTTTTTTTCTTT | 672 |
rs575523120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43116988 | TTCCTATAAACTAGA[C/G]TTACAGGCTTAATCA | 672 |
rs575540881 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115477 | ACTGCACTCCAGCCT[A/G]GGCGACAGAGCGAGA | 672 |
rs575559839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43061263 | TATTTAGGTCTCAGC[A/T]CAATTTTTTCAGAAA | 672 |
rs575579952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43117512 | TTGGGAGGCCGAGGC[A/G]GGCGGATCATGAGGT | 672 |
rs575589035 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107096 | TTGAGACGGAGTCTC[A/G]CTCTGTCTCCCAGGC | 672 |
rs575603008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113082 | TGCTAGGATTAGAGG[C/T]GTGAGCCACCGTGCC | 672 |
rs575618234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43107656 | ACAGGCATGAGCCAC[C/T]GTGCCCAGGCCAAAG | 672 |
rs575697016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43102059 | AGGTGCATACCACCA[C/T]GCCCAGCTAAGTTTT | 672 |
rs575730314 | in-del | -/A | 0.40157 | 0.198813 | intron-variant | BRCA1 | GRCh38.p7 | 17:43108335 | GAGTGAGATTGTGCC[-/A]AAAAAAAAAAAAAAG | 672 |
rs575740869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113915 | CCCTGTCTCGACTAA[A/G]AATACAAAAATTAGC | 672 |
rs575786890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054221 | GCTCACATGGCGCTC[C/T]CCTGTGGTAAAGGCA | 672 |
rs575797081 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050240 | CAAGGCCTTTGTGCT[A/G]CGCAACTCCAGAGGT | 672 |
rs575811491 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073440 | TAAGTAGAATGTATG[A/G]GATTCCTAAAATGAC | 672 |
rs575820341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43068221 | AGCAGAGCTTGCAGT[A/G]AGCCGAGATGGCGCC | 672 |
rs575830513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124428 | CCTTAGCTTTCTCCA[A/G]TGTTTCTGGTTGTTT | 672 |
rs575867878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43060529 | AGGAGTCTTGCTCTG[A/T]CGTTCAGGCTGGAGT | 672 |
rs575912798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43119590 | CTGAGATGACTTGGG[A/G]AAAATGCTTCACAAC | 672 |
rs575952408 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070811 | TAAATTACACAGAAC[A/T]GTGATTGTTTTCTAG | 672 |
rs575962054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079781 | GAATTCATGGCATAA[C/T]AGGTGTTAAAAAAAA | 672 |
rs576063430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105238 | AGAAAACTAGAGTAC[C/T]TTTTTTTTTGTTTAA | 672 |
rs576071621 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076051 | TGAGCCATGACTGCA[A/C]CACTGCAATCTAGGT | 672 |
rs576188703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058216 | TCTAGAAAAAAGATA[C/G]ATAAAACCTCAGCCA | 672 |
rs576228200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43064312 | TGTGGACGGAGAACA[A/T]CTATATTACTAGATG | 672 |
rs576251388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057250 | CGCAGTGGCTCACCC[C/T]TGTAATCCTAGCACT | 672 |
rs576358490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43072991 | CAAAGTACTGAGATT[A/G]CAGGCATGAGCAGTG | 672 |
rs576464426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122187 | CTTGACTTCAAATAT[G/T]AAAAACAACTTTCAT | 672 |
rs576499265 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077165 | CACATTTTCAATTAC[C/T]GAAAAAAAAGAAAAA | 672 |
rs576531149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098444 | GCTCATTGTAACCTC[C/T]GCCTCCCTGGTTCAA | 672 |
rs576534569 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106682 | AATTACAAGCAATAG[A/T]TTCCTAATTGTTTTT | 672 |
rs576562896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098217 | AAATTTTTTTGTAGA[A/G]ATGAGGTCTTGCTAT | 672 |
rs576618433 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071938 | GCGTGTACCCGGGAG[A/G]CAGAGCTTGCAGTGA | 672 |
rs576621034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105884 | CCTGTGAACCCCAGC[A/G]CTTTGGGAGGCCGAG | 672 |
rs576667957 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43078865 | AAGGGTAATGTGCAA[G/T]TTCCAAGGAACCATA | 672 |
rs576707211 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43053069 | TTTTAGTAGAAACGG[A/G]GTTTCACTATGTTGG | 672 |
rs576727185 | snp | C/G | 1.6569e-05 | 0.00287824 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051084 | GCATGTTGGTGAAGG[C/G]CCCATAGCAACAGAT | 672 |
rs576772942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43058278 | TCTTGAAAAGCTGAA[C/G]CTGGAGGATCACTTG | 672 |
rs576828558 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091003 | CTTCAGAGACGCTTG[C/T]TTCACTCTCACACCC | 672 |
rs576863492 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102518 | CGTGCCACCACACCC[A/G]GCTAATTTTTGTATT | 672 |
rs576936175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43120493 | TCTTAAGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 672 |
rs577010874 | in-del | -/T | 0.309154 | 0.242901 | intron-variant | BRCA1 | GRCh38.p7 | 17:43098984 | CACCACCCCGGCTAA[-/T]TTTTTTTTTTTTTTT | 672 |
rs577030447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065556 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 672 |
rs577051957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43113360 | TTATTTTTCCTGGAT[A/G]TATTTTCTTTTCTTT | 672 |
rs577066462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099153 | AAAGGCTTCCTCATC[G/T]AGTACAATTTATCTT | 672 |
rs577085520 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127219 | GCAGGCGCCCGGCAC[A/G]GCCCTGCGCAGGATC | 672 |
rs577088633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43065030 | AGAGATGGGGTTTCA[C/G]CGTGTTAGCCAGGAT | 672 |
rs577180051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43122460 | GTTTACATTCTGTGG[C/G]ACTAGAGATAAAAAA | 672 |
rs577189905 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049736 | AGCTGGAATCCATAT[A/T]CTCAGGGGAATAAAA | 672 |
rs577231253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43059966 | CCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC | 672 |
rs577371346 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43100672 | CATATATATATATAT[-/A]TATATAATATATATA | 672 |
rs577402357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091205 | AATGAAACCAGAAGT[A/C]AGTCCACCAGTAATT | 672 |
rs577434223 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104391 | TAAGGTTACCTGTGA[-/T]TTTTTTTTAAAAATC | 672 |
rs577442222 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067014 | GTAGAGACGGGGTTT[C/T]AACACGTTGGCCAGG | 672 |
rs577465138 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076515 | GGTTCTTTATTTTTA[C/T]TGGTAGAACTATCTG | 672 |
rs577478710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082340 | GTCCTTACTCTTCAG[A/G]AGGAGATAAAGGGGA | 672 |
rs577502686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43078436 | CTTGGCATCTCACAG[C/T]GCTGGGATTATAGGC | 672 |
rs577575111 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122746 | AAACCCTATCTCTAC[A/C]ACAGAAAAATACAAG | 672 |
rs577611867 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | BRCA1 | GRCh38.p7 | 17:43081056 | GTTACAGATCTCCAG[-/A]AAAAAAATAAACACA | 672 |
rs577667582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079997 | CTTAATCCTTAATTC[A/G]TTCTCTGAACAGCAA | 672 |
rs577740757 | snp | C/T | 3.90785e-05 | 0.00442015 | intron-variant | BRCA1 | GRCh38.p7 | 17:43094888 | AAAAATAACAAGGTA[C/T]TCAAAAACTGAATTG | 672 |
rs577927041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048170 | CAGTGTTGTGATTAC[A/G]GGGGTGGGGCACTGG | 672 |
rs577938074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43088950 | AGATAAATAAATGAA[A/T]AAAATAAACTGAGAT | 672 |
rs577956001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43048988 | TACAGATGGAGTCTT[C/T]TGGCACAGGTATGTG | 672 |
rs577992857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43096454 | GTGTATACCTGTAGT[C/T]CCAGCTACTCGTGAG | 672 |
rs578032709 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43054161 | GAGGGGAAGAATCTG[G/T]TGCTAATACTGCCTA | 672 |
rs578047654 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086810 | GCAAAGAGAGAAAAG[A/G]CCTCCTAAATCTTTT | 672 |
rs578061214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | BRCA1 | GRCh38.p7 | 17:43089553 | TTGTGTACTTTCTTT[C/T]TTTTTTTTTTTGAGA | 672 |
rs578075197 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057378 | TAGTTGGGCGTGGTG[C/G]CAGGCACCTGTAATC | 672 |
rs578193281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43103440 | TCACTGCGCTCCAGC[C/G]TGGGCGACAGAGCGA | 672 |
rs578232174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | BRCA1 | GRCh38.p7 | 17:43111588 | GAACTTAGGGAGGCC[A/G]AGGCGGGCAGATCAC | 672 |
rs578250989 | snp | A/G | 4.89512e-05 | 0.00494704 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104071 | TCAAAAAAAAAAAAG[A/G]AAAAAAAAAGAAAAG | 672 |
rs587776478 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094297 | TTAGAACGTCCAATA[C/T]ATCAGCTACTTTGGC | 672 |
rs587776480 | in-del | -/GTTTG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093915 | TGACCATTCTGCTCC[-/GTTTG]GTTAGTTCCCTGATT | 672 |
rs587776481 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093556 | TGCTGTGCCTGACTG[C/G]CATTTGGTTGTACTT | 672 |
rs587776482 | snp | A/G/T | 1.64803e-05 | 0.00287052 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43093189 | AGTAACGAGATACTT[A/G/T]CCTGAGTGCCATAAT | 672 |
rs587776484 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092841 | TCAAAAGTGACTTTT[A/G]GACTTTGTTTCTTTA | 672 |
rs587776485 | in-del | -/CA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104895 | TGTCAAGCTGAAAAG[-/CA]CAAATGATTTTCAAT | 672 |
rs587776487 | snp | C/T | 1.64795e-05 | 0.00287045 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092361 | CCTATTTCATTAATA[C/T]TGGAGCCCACTTCAT | 672 |
rs587776488 | snp | C/T | 1.64754e-05 | 0.00287009 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091795 | ACTCGGTAGCAACGG[C/T]GCTATGCCTAGTAGA | 672 |
rs587776489 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104190 | AGCCCATACTTTGGA[C/T]GATAGAAACTTCATC | 672 |
rs587776492 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049126 | CAATACTTACTGTGC[C/T]AAGGGTGAATGATGA | 672 |
rs587776493 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047719 | CTGGATCCCCAGGAA[A/G]GAAAGAGCATTCAAA | 672 |
rs587777910 | in-del | -/NNNN | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092366 | TACTAATGAAGTGGG[-/NNNN]CTCCAGTATTAATGA | 672 |
rs587777911 | in-del | -/NNNNNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076583 | GAAAAGTAGTGAATA[-/NNNNNNN]CCCTATAAGCCAGAA | 672 |
rs587778115 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099856 | AGTCTCAGTGTCCAA[C/G]TCTCTAACCTTGGAA | 672 |
rs587778116 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093201 | TACCTGGTACTGATT[A/G]TGGCACTCAGGAAAG | 672 |
rs587778117 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092254 | GTTTTGCAACCTGAG[G/T]TCTATAAACAAAGTC | 672 |
rs587779367 | snp | C/G/T | 1.64803e-05 | 0.00287052 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43104224 | AAAAAAGGAAAATAA[C/G/T]TCTCCTGAACATCTA | 672 |
rs587779368 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091976 | CGTCCAGAAAGGAGA[G/T]CTTAGCAGGAGTCCT | 672 |
rs587780794 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094335 | GTTCTGATGACTCAC[A/G]TGATGGGGAGTCTGA | 672 |
rs587780795 | snp | C/G/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093827 | GAATGAGAAAAATCC[C/G/T]AACCCAATAGAATCA | 672 |
rs587780796 | snp | A/G | 0.000115602 | 0.00760182 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093701 | ACCTAAAAAGAATAG[A/G]CTGAGGAGGAAGTCT | 672 |
rs587780797 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106441 | GGTATATAATTTGGT[A/G]ATGATGCTAGGTTGG | 672 |
rs587780798 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093025 | TATCCATTGGGACAT[-/G]AAGTTAACCACAGTC | 672 |
rs587780799 | snp | A/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092588 | CCCATATCGTATACC[A/T]CCACTTTTTCCCATC | 672 |
rs587780800 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104225 | CAAAAAAGGAAAATA[A/G]CTCTCCTGAACATCT | 672 |
rs587780801 | snp | C/T | 8.23757e-05 | 0.00641725 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091784 | TAGCACCGTTGCTAC[C/T]GAGTGTCTGTCTAAG | 672 |
rs587780802 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091657 | GAGGAAACAAAATGT[-/T]CTGCTAGCTTGTTTT | 672 |
rs587780803 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099816 | CTCTGAGGACAAAGC[A/C]GCGGATACAACCTCA | 672 |
rs587780804 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097229 | GGTGAGTCAAAGAGA[A/G]CCTTTGTCTATGAAG | 672 |
rs587780805 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115779 | CCCCTACCCTGCTAG[C/T]CTGGAGTTGATCAAG | 672 |
rs587780862 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091829 | GTTATTTGGTAAAGT[A/G]AACAATATACCTTCT | 672 |
rs587780863 | snp | C/T | 4.9436e-05 | 0.00497148 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43074353 | TTTGACGGAAACATC[C/T]TACTTGCCAAGGCAA | 672 |
rs587780864 | snp | G/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071147 | CCCAGAGTCAGCTCG[G/T]GTTGGCAACATACCA | 672 |
rs587781258 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057124 | TCAGCATGATTTTGA[-/A]GTCAGAGGAGATGTG | 672 |
rs587781315 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093826 | AATGAGAAAAATCCT[A/G]ACCCAATAGAATCAC | 672 |
rs587781420 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093412 | TTAACAAATGCACCT[C/G]GTTCTTTTACTAAGT | 672 |
rs587781423 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092910 | TTGCTCCGTTTTCAA[-/A]TCCAGGAAATGCAGA | 672 |
rs587781427 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099836 | TAACCTTGGAACTGT[-/T]GAGAACTCTGAGGAC | 672 |
rs587781448 | snp | A/G | 1.64819e-05 | 0.00287066 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093463 | AATGAACAGACAAGT[A/G]AAAGACATGACAGCG | 672 |
rs587781472 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067680 | ATGCTCGTGTACAAG[A/T]TTGCCAGAAAACACC | 672 |
rs587781477 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067668 | AAGTTTGCCAGAAAA[C/T]ACCACATCACTTTAA | 672 |
rs587781487 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099809 | GACAAAGCAGCGGAT[-/T]ACAACCTCAAAAGAC | 672 |
rs587781491 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104204 | CTGAACATCTAAAAG[A/G]TGAAGTTTCTATCAT | 672 |
rs587781492 | snp | C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092781 | AGAATGAGTCTAATA[C/G/T]CAAGCCTGTACAGAC | 672 |
rs587781496 | snp | C/T | 3.3071e-05 | 0.00406625 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094732 | CAGGGTAGTTCTGTT[C/T]CAAACTTGCATGTGG | 672 |
rs587781526 | in-del | AATA/TCTATGATCTCTTTAGGGGT | | | intron-variant, splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43063370 | ATGTAACCTGTCTTT[AATA/TCTATGATCTCTTTAGGGGT]GACCCAGTCTATTAA | 672 |
rs587781565 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124097 | ATTGGAACAGAAAGA[A/C]ATGGATTTATCTGCT | 672 |
rs587781588 | snp | C/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092364 | CTAATGAAGTGGGCT[C/G/T]CAGTATTAATGAAAT | 672 |
rs587781611 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076571 | ATACCCTATAAGCCA[-/G]AATCCAGAAGGCCTT | 672 |
rs587781613 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093718 | ATCCACAATTCAAAA[G/T]CACCTAAAAAGAATA | 672 |
rs587781614 | in-del | -/GAA | 6.6066e-05 | 0.00574706 | BRCA1 | 17 | allele_origin=G(germline)/+.-----(germline) | 17:43093705 | AAAAGCACCTAAAAA[-/GAA]TAGGCTGAGGAGGAA | 672 |
rs587781623 | snp | A/C/T | 4.94216e-05 | 0.00497079 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43071124 | ACATACCATCTTCAA[A/C/T]CTCTGCATTGAAAGT | 672 |
rs587781632 | snp | A/T | | | stop-gained, splice-donor-variant | BRCA1 | GRCh38.p7 | 17:43106476 | ACAGTGTCCTTTATG[A/T]AAGAATGATATAACC | 672 |
rs587781641 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092626 | GGACTCATTACTCCA[A/G]ATAAACATGGACTTT | 672 |
rs587781684 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093279 | ACCCCAAAGATCTCA[C/T]GTTAAGTGGAGAAAG | 672 |
rs587781715 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094195 | ATATGTAAAAGTGAA[A/G]GAGTTCACTCCAAAT | 672 |
rs587781737 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094515 | CCAGCACAGAAAAAA[A/C]GGTAGATCTGAATGC | 672 |
rs587781761 | snp | C/T | 1.6473e-05 | 0.00286988 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43099787 | CAAAAGACGTCTGTC[C/T]ACATTGAATTGGGTA | 672 |
rs587781765 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092116 | GAACAGCCTATGGGA[A/C]GTAGTCATGCATCTC | 672 |
rs587781768 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082530 | AAGCTCCAGCAGGAA[A/G]TGGCTGAACTAGAAG | 672 |
rs587781769 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094434 | CAGAGAATCCTAGAG[A/T]TACTGAAGATGTTCC | 672 |
rs587781770 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051074 | ATGGGCCCTTCACCA[A/G]CATGCCCACAGGTAA | 672 |
rs587781771 | snp | A/G/T | | | synonymous-codon, missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092852 | CTCTGGGTCCTTAAA[A/G/T]AAACAAAGTCCAAAA | 672 |
rs587781779 | in-del | -/GAG | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091865 | TCTAGTGAGGATGAA[-/GAG]CTTCCCTGCTTCCAA | 672 |
rs587781781 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093328 | GAAAAAGAAGAGAAA[C/G]TAGAAACAGTTAAAG | 672 |
rs587781798 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104261 | CCTTGTATTTTACAG[A/G]TGCAAACAGCTATAA | 672 |
rs587781825 | in-del | -/GC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051084 | AATCTGTTGCTATGG[-/GC]CCTTCACCAACATGC | 672 |
rs587781833 | snp | A/C/T | 1.65704e-05 | 0.00287836 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43094765 | AAGCGTGCAGCTGAG[A/C/T]GGCATCCAGAAAAGT | 672 |
rs587781876 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071237 | CCCATTCCTTTCAGA[C/G]GGAACCCCTTACCTG | 672 |
rs587781880 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076506 | CTACCAGTAAAAATA[A/G]AGAACCAGGAGTGGA | 672 |
rs587781914 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092847 | GGTCCTTAAAGAAAC[A/G]AAGTCCAAAAGTCAC | 672 |
rs587781916 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106538 | TCTTTCTTTATAATT[C/T]ATAGATTTTGCATGC | 672 |
rs587782012 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071134 | CGTGTTGGCAACATA[C/G]CATCTTCAACCTCTG | 672 |
rs587782017 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104229 | TTTGCAAAAAAGGAA[A/G]ATAACTCTCCTGAAC | 672 |
rs587782019 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049178 | TCAACTGGAATGGAT[A/G]GTACAGCTGTGTGGT | 672 |
rs587782026 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045800 | TCTCTGTCTCCAGCA[A/G]TTGGGCAGATGTGTG | 672 |
rs587782027 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093135 | CAAAAACAGAACCAA[A/G]TAAATGTGTGAGTCA | 672 |
rs587782094 | snp | A/G/T | 1.76213e-05 | 0.00296822 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094818 | TAACAAATACTGAAC[A/G/T]TCATCAACCCAGTAA | 672 |
rs587782097 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045677 | CACAGCCACTACTGA[C/T]TGCAGCCAGCCACAG | 672 |
rs587782123 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094804 | CATCATCAACCCAGT[A/G]ATAATGATTTGAACA | 672 |
rs587782134 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092874 | AATGTGCAACATTCT[C/G]TGCCCACTCTGGGTC | 672 |
rs587782143 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074350 | GACGGAAACATCTTA[-/A]CTTGCCAAGGCAAGA | 672 |
rs587782173 | snp | A/C/G/T | 4.94592e-05 | 0.0049727 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43104867 | ACACAGGTTTGGAGT[A/C/G/T]TAAGTGTTGAATATC | 672 |
rs587782188 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091996 | TCTGCTGTTTTTAGC[A/C]AAAGCGTCCAGAAAG | 672 |
rs587782190 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091731 | CATTGAAGAATAGCT[C/T]AAATGACTGCAGTAA | 672 |
rs587782241 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091561 | GGTTCTTCCAAACAA[A/T]TGAGGCATCAGTCTG | 672 |
rs587782251 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094043 | GATAATACAAGAGCG[-/T]CCCCTCACAAATAAA | 672 |
rs587782340 | snp | C/T | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045772 | GTGAGGCACCTGTGG[C/T]GACCCGAGAGTGGGT | 672 |
rs587782370 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092893 | CCAGGAAATGCAGAA[C/G]AGGAATGTGCAACAT | 672 |
rs587782390 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093895 | CAGAATGGTCAAGTG[A/G]TGAATATTACTAATA | 672 |
rs587782392 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071114 | TTCAACCTCTGCATT[-/T]GAAAGTTCCCCAATT | 672 |
rs587782432 | snp | A/G | 1.64762e-05 | 0.00287016 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43045789 | AGCAATTGGGCAGAT[A/G]TGTGAGGCACCTGTG | 672 |
rs587782456 | snp | A/C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063879 | AATGGGTAGTTAGCT[A/C/G]TTTCTGTAAGTATAA | 672 |
rs587782458 | snp | C/T | 6.62921e-05 | 0.00575688 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091935 | CCCATACACATTTGG[C/T]TCAGGGTTACCGAAG | 672 |
rs587782595 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093455 | GACAAGTAAAAGACA[A/T]GACAGCGATACTTTC | 672 |
rs587782606 | snp | C/T | 1.6483e-05 | 0.00287076 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43076611 | TTCCATTTAAAGCAG[C/T]ATTAACTTCACAGAA | 672 |
rs587782608 | snp | A/G | 1.64779e-05 | 0.00287031 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092918 | CCAGTCATTTGCTCC[A/G]TTTTCAAATCCAGGA | 672 |
rs587782628 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092938 | ACATTCAAGGTTTCA[A/T]AGCGCCAGTCATTTG | 672 |
rs587782630 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092404 | GAAGCCAGCTCAAGC[A/G]ATATTAATGAAGTAG | 672 |
rs587782634 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091575 | ATCCTTTCTTGATTG[A/G]TTCTTCCAAACAAAT | 672 |
rs587782663 | in-del | -/CTTTACCATACTGTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099884 | AATTGCTTGACTGTT[-/CTTTACCATACTGTT]TAGCAGGAAACCAGT | 672 |
rs587782666 | in-del | -/ATAA | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104225 | TTGCAAAAAAGGAAA[-/ATAA]CTCTCCTGAACATCT | 672 |
rs587782708 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076560 | GCCAGAATCCAGAAG[C/G]CCTTTCTGCTGACAA | 672 |
rs587782709 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093475 | AGTAACAAGCCAAAT[G/T]AACAGACAAGTAAAA | 672 |
rs587782721 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092616 | CTCCAAATAAACATG[A/G]ACTTTTACAAAACCC | 672 |
rs587782724 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104151 | CGTGCCAAAAGACTT[C/G]TACAGAGTGAACCCG | 672 |
rs587782739 | in-del | -/GTT | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093598 | TGCAAATTGATAGTT[-/GTT]CTAGCAGTGAAGAGA | 672 |
rs587782743 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092654 | ATCATCTCAGTTCAG[A/C]GGCAACGAAACTGGA | 672 |
rs587782747 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099795 | TACAACCTCAAAAGA[C/G]GTCTGTCTACATTGA | 672 |
rs587782749 | in-del | AG/NNNNNNNNNNNNNNNNNNNNNN | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104930 | GAAAGTACGAGATTT[AG/NNNNNNNNNNNNNNNNNNNNNN]TCAACTTGTTGAAGA | 672 |
rs587782752 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092082 | TTTGTTCTGAGACAC[C/T]TGATGACCTGTTAGA | 672 |
rs587782770 | snp | A/G | 8.24858e-05 | 0.00642153 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094288 | GCTGATGTATTGGAC[A/G]TTCTAAATGAGGTAG | 672 |
rs587782778 | snp | C/G | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045778 | AGATGTGTGAGGCAC[C/G]TGTGGTGACCCGAGA | 672 |
rs587782784 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094192 | TGTAAAAGTGAAAGA[A/G]TTCACTCCAAATCAG | 672 |
rs587782790 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094453 | AAGCAGAAACTGCCA[C/T]GCTCAGAGAATCCTA | 672 |
rs587782821 | in-del | -/AAG | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092184 | GCAAGAATATGAAGA[-/AAG]GTAGTTCAGACTGTT | 672 |
rs587782824 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091951 | AGTCCTAGCCCTTTC[-/T]ACCCATACACATTTG | 672 |
rs587782825 | snp | A/G | 1.64795e-05 | 0.00287045 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43071143 | GAGTCAGCTCGTGTT[A/G]GCAACATACCATCTT | 672 |
rs587782834 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091561 | TGGTTCTTCCAAACA[-/AA]TGAGGCATCAGTCTG | 672 |
rs587782843 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093611 | TTGTACTGAATTGCA[A/T]ATTGATAGTTGTTCT | 672 |
rs587782864 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092242 | GAGGTCTATAAACAA[A/T]GTCTTCCTGGAAGTA | 672 |
rs587782870 | snp | A/C/G | 2.24575e-05 | 0.00335086 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43090952 | CAGAGTGACATTTTA[A/C/G]CCACTCAGGTAAAAA | 672 |
rs587782873 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047697 | GGGATCCAGGGTGTC[C/T]ACCCAATTGTGGTTG | 672 |
rs587782879 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082511 | CTGAACTAGAAGCTG[-/T]GTTAGAACAGCATGG | 672 |
rs587782882 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104205 | CCTGAACATCTAAAA[A/G]ATGAAGTTTCTATCA | 672 |
rs587782887 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045794 | TCTCCAGCAATTGGG[A/C]AGATGTGTGAGGCAC | 672 |
rs587783039 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093764 | TGAACCTATAAGCAG[A/C]AGTATAAGCAATATG | 672 |
rs587783040 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106524 | TTATAGATTTTGCAT[A/G]CTGAAACTTCTCAAC | 672 |
rs587783041 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093865 | AGTGGTCATGAGAAT[A/C]AAACAAAAGGTGATT | 672 |
rs606231389 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093374 | TACCAGTGAACTTAA[-/A]AGAATTTGTCAATCC | 672 |
rs606231390 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092839 | AAGAAACAAAGTCCA[-/A]AAAGTCACTTTTGAA | 672 |
rs606231391 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092425 | ATTAGAGAAAATGTT[-/T]TTTAAAGAAGCCAGC | 672 |
rs606231392 | in-del | -/A | | | frameshift-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43106463 | TGTAAGAATGATATA[-/A]ACCAAAAGGTATATA | 672 |
rs606231393 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091907 | AAGAGGGGCCAAGAA[-/A]ATTAGAGTCCTCAGA | 672 |
rs606231394 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051108 | TTCCAGATCTTCAGG[-/G]GGGCTAGAAATCTGT | 672 |
rs606231395 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049142 | TGTGGTGAAGGAGCT[-/T]TTCATCATTCACCCT | 672 |
rs730880287 | in-del | AG/GCC | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071076 | GCAGAATCTGCCCAG[AG/GCC]TCCAGCTGCTGCTCA | 672 |
rs730880288 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063893 | AATTGCGGGAGGAAA[-/A]TGGGTAGTTAGCTAT | 672 |
rs730881439 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092593 | CAAAACCCATATCGT[-/A]TACCACCACTTTTTC | 672 |
rs730881440 | in-del | -/CA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091763 | GTCTGTCTAAGAACA[-/CA]GAGGAGAATTTATTA | 672 |
rs730881441 | in-del | -/GGCAGATG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045789 | TGTCTCCAGCAATTG[-/GGCAGATG]TGTGAGGCACCTGTG | 672 |
rs730881442 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094272 | TTCTAAATGAGGTAG[A/G]TGAATATTCTGGTTC | 672 |
rs730881443 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092643 | TCAGAGGCAACGAAA[C/T]TGGACTCATTACTCC | 672 |
rs730881444 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091551 | AACAAATGAGGCATC[A/G]GTCTGAAAGCCAGGG | 672 |
rs730881445 | snp | C/G/T | | | missense, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082456 | TTCCATCATAAGTGA[C/G/T]TCTTCTGCCCTTGAG | 672 |
rs730881446 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049149 | GTGCTTCTGTGGTGA[A/C]GGAGCTTTCATCATT | 672 |
rs730881447 | snp | A/C | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045742 | TGTTGGACAGTGTAG[A/C]ACTCTACCAGTGCCA | 672 |
rs730881448 | snp | C/G/T | 1.64746e-05 | 0.00287002 | BRCA1 | 17 | allele_origin=G(germline)/T(germline)/C(germline) | 17:43104143 | AAGACTTCTACAGAG[C/G/T]GAACCCGAAAATCCT | 672 |
rs730881449 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104106 | GTAAAACCATTTGTT[-/T]TCTTCTTCTTCTTCT | 672 |
rs730881450 | in-del | -/TTC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104104 | GTAAAACCATTTGTT[-/TTC]TTCTTCTTCTTCTTC | 672 |
rs730881451 | snp | A/G | 0.000115332 | 0.00759293 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092897 | AAATCCAGGAAATGC[A/G]GAAGAGGAATGTGCA | 672 |
rs730881452 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092671 | GGCTCTAGGTTTTGT[C/T]TATCATCTCAGTTCA | 672 |
rs730881453 | snp | A/T | 0.000115322 | 0.00759261 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43091814 | AAACAATATACCTTC[A/T]CAGTCTACTAGGCAT | 672 |
rs730881454 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091631 | GTTTTCTTCACAGTG[C/T]AGTGAATTGGAAGAC | 672 |
rs730881455 | snp | A/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076553 | TCCAGAAGGCCTTTC[A/T]GCTGACAAGTTTGAG | 672 |
rs730881456 | snp | C/T | 1.64798e-05 | 0.00287047 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43047698 | GGGGATCCAGGGTGT[C/T]CACCCAATTGTGGTT | 672 |
rs730881457 | in-del | -/T | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124052 | AGTACAAAATGTCAT[-/T]AATGCTATGCAGAAA | 672 |
rs730881458 | in-del | -/TT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094190 | GTAAAAGTGAAAGAG[-/TT]CACTCCAAATCAGTA | 672 |
rs730881459 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093671 | TTCTACCAGGCATAT[-/T]CATGCGCTTGAACTA | 672 |
rs730881460 | multinucleotide-polymorphism | AC/GA | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092892 | CCAGGAAATGCAGAA[AC/GA]GGAATGTGCAACATT | 672 |
rs730881461 | in-del | -/C | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092586 | CATATCGTATACCAC[-/C]ACTTTTTCCCATCAA | 672 |
rs730881462 | in-del | -/TATTAATGAA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092393 | AGCCAGCTCAAGCAA[-/TATTAATGAA]GTAGGTTCCAGTACT | 672 |
rs730881463 | in-del | -/AGA | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082572 | TATCGTTTTTGAAGC[-/AGA]GGGATACCATGCAAC | 672 |
rs730881464 | multinucleotide-polymorphism | GC/TT | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074391 | TGTGGAGGAGCAACA[GC/TT]TGGAAGAGTCTGGGC | 672 |
rs730881465 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104947 | TTTCAGGAGCCTACA[A/C]GAAAGTACGAGATTT | 672 |
rs730881466 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095891 | TTGTTACAAATCACC[C/T]CTCAAGGAACCAGGG | 672 |
rs730881467 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094802 | TCATCAACCCAGTAA[G/T]AATGATTTGAACACC | 672 |
rs730881468 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094662 | ATGAGAACAGCAGTT[G/T]ATTACTCACTAAAGA | 672 |
rs730881469 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094299 | ATGCCAAAGTAGCTG[A/T]TGTATTGGACGTTCT | 672 |
rs730881470 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094218 | CCAGTGATCCTCATG[A/C]GGCTTTAATATGTAA | 672 |
rs730881471 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093913 | GGAACTAACCAAACG[A/G]AGCAGAATGGTCAAG | 672 |
rs730881472 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093880 | ATGAATATTACTAAT[A/G]GTGGTCATGAGAATA | 672 |
rs730881473 | snp | C/G/T | | | missense, stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093817 | AATCCTAACCCAATA[C/G/T]AATCACTCGAAAAAG | 672 |
rs730881474 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093609 | GTACTGAATTGCAAA[C/T]TGATAGTTGTTCTAG | 672 |
rs730881475 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093492 | CAACTGGAGCCAAGA[A/G]GAGTAACAAGCCAAA | 672 |
rs730881476 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093441 | ATGACAGCGATACTT[C/T]CCCAGAGCTGAAGTT | 672 |
rs730881477 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093388 | ACTAAGTGTTCAAAT[A/T]CCAGTGAACTTAAAG | 672 |
rs730881478 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093383 | GTGTTCAAATACCAG[A/T]GAACTTAAAGAATTT | 672 |
rs730881479 | snp | A/G/T | 1.6477e-05 | 0.00287024 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43093285 | CTGAAGACCCCAAAG[A/G/T]TCTCATGTTAAGTGG | 672 |
rs730881480 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093272 | AGATCTCATGTTAAG[G/T]GGAGAAAGGGTTTTG | 672 |
rs730881481 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093219 | GTAGCAGTATTTCAT[C/T]GGTACCTGGTACTGA | 672 |
rs730881482 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093210 | TTTCATTGGTACCTG[A/G]TACTGATTATGGCAC | 672 |
rs730881483 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093198 | CTGGTACTGATTATG[A/G]CACTCAGGAAAGTAT | 672 |
rs730881484 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093087 | ACCCCAAGGGACTAA[C/T]TCATGGTTGTTCCAA | 672 |
rs730881485 | snp | G/T | 4.94287e-05 | 0.00497111 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43092723 | GGTTGGTCAGAAAGA[G/T]AAGCCAGTTGATAAT | 672 |
rs730881486 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092685 | GTAGTATCAAAGGAG[A/G]CTCTAGGTTTTGTCT | 672 |
rs730881487 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092609 | TAAACATGGACTTTT[A/C]CAAAACCCATATCGT | 672 |
rs730881488 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091850 | GCTTCCCTGCTTCCA[A/T]CACTTGTTATTTGGT | 672 |
rs730881489 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091701 | ACCAGGTAATATTGG[C/T]AAAGGCATCTCAGGA | 672 |
rs730881490 | snp | G/T | 1.64757e-05 | 0.00287012 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43091536 | AGTCTGAAAGCCAGG[G/T]AGTTGGTCTGAGTGA | 672 |
rs730881491 | snp | A/G | 1.95708e-05 | 0.0031281 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43091000 | TGTGAGAGTGAAACA[A/G]GCGTCTCTGAAGACT | 672 |
rs730881492 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074367 | TCTGGGCCACACGAT[A/T]TGACGGAAACATCTT | 672 |
rs730881493 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071218 | ACCCCTTACCTGGAA[G/T]CTGGAATCAGCCTCT | 672 |
rs730881494 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071040 | CTGATACTGCTGGGT[A/G]TAATGCAATGGAAGA | 672 |
rs730881495 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43067696 | TTTGATTTAATTTCA[A/G]ATGCTCGTGTACAAG | 672 |
rs730881496 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063340 | AAGAAAGAAAAATGC[A/T]GAATGAGGTAAGTAC | 672 |
rs730881497 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051092 | GGCTAGAAATCTGTT[A/G]CTATGGGCCCTTCAC | 672 |
rs730881498 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43045807 | CTTGTGTTCTCTGTC[G/T]CCAGCAATTGGGCAG | 672 |
rs730881499 | snp | A/T | 3.29522e-05 | 0.00405894 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43045793 | CTCCAGCAATTGGGC[A/T]GATGTGTGAGGCACC | 672 |
rs730881500 | snp | C/T | 1.64781e-05 | 0.00287033 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43045769 | AGGCACCTGTGGTGA[C/T]CCGAGAGTGGGTGTT | 672 |
rs730881501 | snp | A/G/T | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045758 | GTGACCCGAGAGTGG[A/G/T]TGTTGGACAGTGTAG | 672 |
rs730881502 | snp | C/T | | | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045715 | GCCAGGAGCTGGACA[C/T]CTACCTGATACCCCA | 672 |
rs730882056 | in-del | -/CC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092718 | GGTCAGAAAGATAAG[-/CC]AGTTGATAATGCCAA | 672 |
rs730882057 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091981 | CAAAAGCGTCCAGAA[-/AG]GAGAGCTTAGCAGGA | 672 |
rs730882075 | in-del | -/AG | | | splice-acceptor-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124115 | TCTAATGTGTTAAAG[-/AG]TTCATTGGAACAGAA | 672 |
rs730882164 | snp | A/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092020 | GCTGAAAATGACATT[A/T]AGGAAAGTTCTGCTG | 672 |
rs730882165 | snp | A/C/G/T | | | stop-gained, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067684 | TCAGATGCTCGTGTA[A/C/G/T]AAGTTTGCCAGAAAA | 672 |
rs730882166 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067625 | CTGAAGAGACTACTC[A/G]TGTTGTTATGAAAAC | 672 |
rs730882167 | in-del | A/TTT | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063359 | GGGGTGACCCAGTCT[A/TTT]TTAAAGAAAGAAAAA | 672 |
rs745316469 | in-del | -/AC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058379 | CTCTGCTAAAAAAAA[-/AC]ACACACACACACACA | 672 |
rs745321499 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099827 | CCGCTGCTTTGTCCT[C/T]AGAGTTCTCACAGTT | 672 |
rs745330659 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073195 | TTATCTTTTTTATTC[C/T]CTATATTGTCCAATT | 672 |
rs745341832 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057446 | AATGCAGGAGGTGGA[C/G]GTTGCAGTGAGCTGA | 672 |
rs745363083 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127442 | TAAATGCACCAATCA[A/G]TGCTCTGTGTCTAGC | 672 |
rs745366396 | snp | G/T | 4.97434e-05 | 0.00498691 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082362 | TAAAGGGGAAGGAAA[G/T]AATTTTGCTTAAGAT | 672 |
rs745418679 | snp | C/G | 1.64885e-05 | 0.00287123 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092035 | TAATGTCATTTTCAG[C/G]AAAACTAGTATCTTC | 672 |
rs745434160 | in-del | -/TGGT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082238 | TTGGGTCCCTCTGAC[-/TGGT]TGGTATATTAGTTGT | 672 |
rs745476489 | snp | A/C | 0.000185684 | 0.00963366 | intron-variant, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125267 | TTTCCCGGGACTCTA[A/C]TACCTTTACCCAGAG | 672 |
rs745516448 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058706 | TCCTAAATCAATTGT[A/G]TATTATCATCTAAGG | 672 |
rs745557486 | in-del | -/AAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081130 | AAGTCACACAATAAT[-/AAC]ATTTTAAATCTTACA | 672 |
rs745573228 | snp | C/G | 1.6596e-05 | 0.00288058 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051035 | CAAAGGCTGGTGCTG[C/G]AACTCTGGGGTTCTC | 672 |
rs745591448 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113599 | GTCTTAATTTCCTGA[C/T]CTCGTGATCCGCCCA | 672 |
rs745603698 | in-del | -/GT | 0.000252048 | 0.0112232 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044859 | CCAGGCTGGAGTGCC[-/GT]GTGGTATGATCTTGG | 672 |
rs745613284 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102721 | GCAGTGGAGTGATCA[C/T]AGCTCACTGTAGTCT | 672 |
rs745638837 | snp | A/T | 1.64795e-05 | 0.00287045 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091497 | CCCGTTCCTCTTTCT[A/T]CATCATCTGAAACCA | 672 |
rs745659312 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117805 | TTCCCATCCCTACCT[C/G]TCTATCCACAAAACC | 672 |
rs745710399 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048690 | TGGCTACTTTTTGTT[G/T]TTTTTTTTTTAGTAC | 672 |
rs745752144 | snp | A/G | 1.67354e-05 | 0.00289265 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045652 | TTCTTGGGGTCCTGT[A/G]GCTCTGTACCTGTGG | 672 |
rs745776983 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089610 | TGGAGAGCAGCAGCA[C/T]GATCTCAGCTCACTG | 672 |
rs745806237 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050335 | TGGAGAGGGCTGGGC[A/G]CAGTGGCTCATGCCT | 672 |
rs745842604 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104447 | TTTACTCCTAGGAAA[C/G]AAAAACAAATACACA | 672 |
rs745877543 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077094 | GCTTCTGCATGTCGG[A/G]GGTAAACAAGACATG | 672 |
rs745954644 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092712 | CTACATTTGGCATTA[C/T]CAACTGGCTTATCTT | 672 |
rs746016001 | snp | A/T | 3.30475e-05 | 0.00406481 | intron-variant | BRCA1 | GRCh38.p7 | 17:43094878 | GAAAATATACAAAAA[A/T]AACAAGGTACTCAAA | 672 |
rs746045640 | snp | C/G | 0.000142788 | 0.0084483 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074549 | ATGGAAGGAGAAAAC[C/G]ATCGCCACCAATTGT | 672 |
rs746053013 | in-del | -/AAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110588 | GTAAGACCCTGTCTC[-/AAA]AAAAAAAAAAAAAAG | 672 |
rs746054547 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063118 | TGGTCTTGAACTCCC[A/G]ACATCAGGTGATCCA | 672 |
rs746061260 | snp | A/G | 2.16392e-05 | 0.00328924 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115809 | GGGGAGAAAAAGAAA[A/G]TAAATGAGGCTCAAT | 672 |
rs746067447 | snp | C/T | 4.97401e-05 | 0.00498674 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094763 | ATACTTTTCTGGATG[C/T]CTCTCAGCTGCACGC | 672 |
rs746155740 | in-del | -/ACA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059470 | GAACGAGATGCTGTC[-/ACA]ACAACAACAACAACA | 672 |
rs746156772 | in-del | -/AAAAGA | 0.000118099 | 0.00768345 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104082 | AAAGAAAAAAAAAAG[-/AAAAGA]AGAAGAAGAAGAAGA | 672 |
rs746162883 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116692 | CCCGGCTGATTTTTC[A/G]TATTTTTAGTAGAGT | 672 |
rs746187092 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044539 | AAAGGAAAAAAATCA[A/C]CTCAAAGAAAGCAAC | 672 |
rs746199881 | snp | A/C | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071012 | CAATTCTGGCTTCTC[A/C]CTGCTCACACTTTCT | 672 |
rs746215605 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122997 | GGGAGGCAGAGTTTG[C/T]AGTGAGCTGAGATCG | 672 |
rs746360085 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054906 | AGGTGCCTACCACCA[C/T]GCCCAGTTAACTTTT | 672 |
rs746372367 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069534 | GAACGCTAATTTTCA[A/G]TGAATAAATAAGGAA | 672 |
rs746394738 | snp | A/G | 1.64789e-05 | 0.0028704 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092360 | ACCTATTTCATTAAT[A/G]CTGGAGCCCACTTCA | 672 |
rs746395832 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054049 | TACTATGGTGACATT[C/T]AGTATTTTCAGAATG | 672 |
rs746407418 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060109 | GAGTTTCACTCTTGT[A/T]GCCCAGGCTGGAGTG | 672 |
rs746446434 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108473 | CCCAGGAGGCTGAGG[C/T]AGGCAGATCACTTGA | 672 |
rs746466049 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088032 | GCTGGGATTACAGGT[A/G]TAAGCCACTGTGCCT | 672 |
rs746485760 | snp | A/C | 0.000185649 | 0.00963277 | intron-variant, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125245 | CATCACTTGGGCCCC[A/C]TGTCCCTTTCCCGGG | 672 |
rs746489632 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069975 | TTTCGCTCTTGTTGC[C/G]CAGGCTGGAGTGCAA | 672 |
rs746498642 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125248 | CACTTGGGCCCCCTG[C/T]CCCTTTCCCGGGACT | 672 |
rs746509819 | snp | G/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123749 | AGATTCCTGCCCCAG[G/T]GCAGAACCAATCAAG | 672 |
rs746516195 | snp | C/T | 3.33372e-05 | 0.00408258 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049233 | AATCACTGCAGTAAT[C/T]TGCATACTTAACCCA | 672 |
rs746538666 | in-del | -/TG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100547 | ATATACATATATATG[-/TG]TGTGTGTGTGTATAT | 672 |
rs746552228 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052924 | CACTGTCGCCTGGGC[A/T]GGAGTGCAATGGTGC | 672 |
rs746575771 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085839 | TTCACATTCATTACA[C/T]ATAAATATATATATA | 672 |
rs746607568 | in-del | -/ATCT | 9.92375e-05 | 0.00704336 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045697 | TAGTGGCTGTGGGGG[-/ATCT]GGGGTATCAGGTAGG | 672 |
rs746661876 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057323 | GACACCAGTCTGACC[A/C]ACATGGTGAAACCTC | 672 |
rs746708666 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055342 | AAGAAACTATAGTAT[C/T]GTTGTTAAGAGTTTA | 672 |
rs746727823 | snp | C/G | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092697 | GAGCCTCCTTTGATA[C/G]TACATTTGGCATTAT | 672 |
rs746734036 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107363 | CCACCATGCCTGGCC[A/G]ACGATTTTTATTTTC | 672 |
rs746748977 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116566 | TTTTGTAGCCCAGAC[C/T]GGCATGCAATGGTGC | 672 |
rs746775027 | snp | A/G | 3.31219e-05 | 0.00406938 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067592 | GCAAGGTATTCTGTA[A/G]AGGTTCTTGGTATAC | 672 |
rs746801074 | snp | A/G | 3.72648e-05 | 0.00431636 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045523 | AAGGGACCCTTGCAT[A/G]GCCAGAAGTCCTTTT | 672 |
rs746801950 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115226 | TAATATATGTCAGTC[A/G]GGTGTGGTGGCTCAC | 672 |
rs746872895 | snp | C/T | 0.000162862 | 0.00902244 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079435 | TAGACATCAAGGGAA[C/T]GGGTACTGTTCAAAA | 672 |
rs746922157 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121966 | ATTGTCATGAGTAAG[-/T]TTTGTGCTTTTTCAA | 672 |
rs746927911 | snp | C/T | 8.28288e-05 | 0.00643487 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099732 | TATAAGATAAGGAAT[C/T]CAGCAATTATTATTA | 672 |
rs746932436 | snp | C/G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047288 | AATTTGTTGTACAGA[C/G/T]GAAGTCTCCTTATGT | 672 |
rs746947639 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086447 | CTATATACTTTTTCT[C/T]GGTTCAGTACAAAAA | 672 |
rs746949187 | snp | C/T | 1.64939e-05 | 0.0028717 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092013 | CTAAAAACAGCAGAA[C/T]TTTCCTTAATGTCAT | 672 |
rs746972533 | snp | G/T | 1.8394e-05 | 0.0030326 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079329 | AAGGGAAAGAGGAGA[G/T]GCACCTGATATATGT | 672 |
rs746978998 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062977 | CTCACTGCAACCCCC[A/G]CCTCCCAGGTTCAAG | 672 |
rs746985073 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110133 | TCTCCTGACCTCGTG[A/T]TGTGCCCATCTCAGC | 672 |
rs747012712 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101160 | TTAGCTCTATATCTT[C/T]TGAAAAATGAATGCT | 672 |
rs747016607 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075163 | TGCCACTCACTCTAT[A/T]CACAATATTCTACTT | 672 |
rs747046197 | snp | C/T | 1.64917e-05 | 0.00287151 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093400 | TGGTATTTGAACACT[C/T]AGTAAAAGAACCAGG | 672 |
rs747116732 | in-del | -/AAAA | 0.0942124 | 0.195526 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110588 | GTAAGACCCTGTCTC[-/AAAA]AAAAAAAAAAAAAGT | 672 |
rs747119850 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122817 | TTTGGGAGGCCCAGG[A/C]GGGTGGATCACAAGG | 672 |
rs747147380 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045018 | CATGTTGGCCAGGCT[A/G]GTTTCGAACTCCTGA | 672 |
rs747172803 | snp | C/G | 6.59185e-05 | 0.00574064 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094653 | TTCATTCTGTCTTTA[C/G]TGAGTAATAAACTGC | 672 |
rs747190736 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126837 | TTGCGGGGAAGTGTG[A/G]AGGGAGAGGCGGGTG | 672 |
rs747212786 | snp | C/T | 1.71428e-05 | 0.00292765 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106520 | TCTGGTTGAGAAGTT[C/T]CAGCATGCAAAATCT | 672 |
rs747230501 | snp | G/T | 1.66164e-05 | 0.00288235 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091401 | TCACTTCTATAAATA[G/T]ACTGGGGCAAACACA | 672 |
rs747236504 | in-del | -/AAACAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065683 | CAAAAACAAAAACAA[-/AAACAG]AAACAAAAGAATCAT | 672 |
rs747287311 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092826 | TCCTTTTGTTCACAT[C/T]CAAAAGTGACTTTTG | 672 |
rs747328587 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081667 | TAAAAATCTGCCTGA[C/T]GTATTGTCTTTCCAA | 672 |
rs747364414 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082496 | TTAGAAGGCTGGCTC[C/T]CATGCTGTTCTAACA | 672 |
rs747373266 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119873 | AACACACTGTAAACA[C/T]AAACTTTGAACAGAT | 672 |
rs747392525 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073369 | ATTAAAAACAGCAGA[A/G]ATGTCATCCTTGAAA | 672 |
rs747448886 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063732 | AGTGATATTAAAGAT[A/G]AAAGTAGTTTAGTAT | 672 |
rs747524894 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083491 | GAAAAAGCAAAAAGC[G/T]AATTCATGAATCTAT | 672 |
rs747539984 | snp | A/G | 1.65468e-05 | 0.00287631 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074503 | ATCATCTAATGATGG[A/G]CATTTAGAAGGGGAT | 672 |
rs747591059 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055886 | TGAAGGTTGCAGTGA[A/G]CAGAGATAGTGGCAC | 672 |
rs747592134 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083837 | TATGTAAGGAGTTTT[A/C]CAAAATATCCTTCTT | 672 |
rs747618610 | snp | C/T | 8.29387e-05 | 0.00643914 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124001 | CCCAAATTAATACAC[C/T]CTTGTGCTGACTTAC | 672 |
rs747649874 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092998 | TTTCTTCCATTTCTA[C/T]GCTTGTTTCCCGACT | 672 |
rs747688901 | snp | A/C/G | 1.64727e-05 | 0.00286986 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43071078 | AGCAGCAGCTGGACT[A/C/G]TGGGCAGATTCTGCA | 672 |
rs747694453 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070972 | CCATGGACATTCTTT[C/T]GTTGACCCTTTCTGT | 672 |
rs747727601 | snp | A/T | 1.64912e-05 | 0.00287147 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094341 | TCCCCATCATGTGAG[A/T]CATCAGAACCTAACA | 672 |
rs747733248 | snp | A/T | 3.32552e-05 | 0.00407756 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104271 | TTGCATCTGTAAAAT[A/T]CAAGGGAAAACATTA | 672 |
rs747857055 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086229 | GCTAATGCATTAGTA[C/T]ACCCAAATGGAACAC | 672 |
rs747870666 | in-del | -/A | 1.81243e-05 | 0.00301029 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079414 | TCTGTAAGAAAGGTG[-/A]AATTGTAGACATCAA | 672 |
rs747889878 | in-del | -/AAAGA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074964 | AAAAGGAAAGGAAAG[-/AAAGA]AAAGAAAAGGAAGGG | 672 |
rs747894403 | snp | A/G | 1.85579e-05 | 0.00304608 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079299 | TTTCAGTAATTTGCC[A/G]AAATGACGAACACAA | 672 |
rs747918176 | snp | A/T | 1.67587e-05 | 0.00289466 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097312 | ATTTCCCCCCAAAAA[A/T]TAAATCAATAAAAGT | 672 |
rs747918612 | in-del | -/AAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090051 | AGATTTTAAAAGGGA[-/AAA]AAAAAAAGAAGAAGA | 672 |
rs747929879 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110740 | ACCATTTTGGGAGGT[A/G]GAGGTGGGCGGATCA | 672 |
rs747958543 | snp | C/T | 2.10924e-05 | 0.00324742 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095970 | CACTAGTTACATGTA[C/T]GCAGAACTGTCAAAT | 672 |
rs748057929 | snp | G/T | 3.38926e-05 | 0.00411645 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124106 | ATCCATTTCTTTCTG[G/T]TCCAATGAACTTTAA | 672 |
rs748067707 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097524 | TGAGGAGGCCGAGAT[A/G]GGTGGATTATTTGAG | 672 |
rs748095428 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044610 | AATATTCATGCCAGA[C/G]GTCTTATATTTTAAG | 672 |
rs748156170 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094549 | TCCGCCTATCATTAC[A/G]TGTTTCCTTACTTCC | 672 |
rs748176375 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105237 | TAGAAAACTAGAGTA[A/C]TTTTTTTTTTGTTTA | 672 |
rs748196793 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048121 | GGCTGGTCTTCAGCT[A/C]CCAGGCTCAAGCGAT | 672 |
rs748228826 | snp | A/G | 1.67103e-05 | 0.00289048 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091394 | ATTTAGCTCACTTCT[A/G]TAAATAGACTGGGGC | 672 |
rs748285767 | snp | A/C/T | 1.64817e-05 | 0.00287064 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092666 | GCCTCTGAACTGAGA[A/C/T]GATAGACAAAACCTA | 672 |
rs748297724 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43091166 | AAATTCCTTGCTTTG[A/G]GACACCTGGATTTGC | 672 |
rs748299111 | snp | C/T | 2.47467e-05 | 0.00351749 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045492 | TTCCAAGGGAGACTT[C/T]AAGCAGAAAATCTTT | 672 |
rs748319423 | snp | C/T | 1.65266e-05 | 0.00287455 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104982 | ATTGTTTGAGAAACA[C/T]ACTCAGCAAGTGATT | 672 |
rs748410422 | snp | A/C | 3.3036e-05 | 0.0040641 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092531 | TTCCTCAAAGTTTTC[A/C]TCTAGCAGATTTTTC | 672 |
rs748431827 | snp | C/G/T | 3.30447e-05 | 0.00406464 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43093873 | TTTGTTTTATTCTCA[C/G/T]GACCACTATTAGTAA | 672 |
rs748472307 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089926 | GTAGGAGGATCGCTT[C/G]AGCCCAGGAAGTCAA | 672 |
rs748550848 | snp | A/C | 1.64953e-05 | 0.00287182 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093378 | TTGACAAATTCTTTA[A/C]GTTCACTGGTATTTG | 672 |
rs748556265 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111656 | GAAACCCTTTCTCTA[C/T]TAAAAATACAAAAAA | 672 |
rs748635552 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064980 | GGACTACAGATGCCC[A/G]CCACCATGCCCGGCT | 672 |
rs748637378 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081544 | ATCACTGAGCTAGGA[A/G]TGAAGTGTACTTTGG | 672 |
rs748665512 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096464 | GTAGTCCCAGCTACT[C/T]GTGAGATTGAGACAG | 672 |
rs748674194 | snp | A/C | 1.64808e-05 | 0.00287057 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091483 | TATTTTCTTCCAAGC[A/C]CGTTCCTCTTTCTTC | 672 |
rs748675395 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094645 | TTTCTACATTCATTC[C/T]GTCTTTAGTGAGTAA | 672 |
rs748700252 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114907 | TATTAAGAAACAAAC[A/G]TTTTCATTTCAAAAG | 672 |
rs748714307 | in-del | -/T | 1.64901e-05 | 0.00287137 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094341 | TCCCCATCATGTGAG[-/T]CATCAGAACCTAACA | 672 |
rs748725643 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080247 | TTGTACAGGGTATTG[C/T]GAAGAATTAAGGAAG | 672 |
rs748760407 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060105 | GATGGAGTTTCACTC[G/T]TGTTGCCCAGGCTGG | 672 |
rs748807039 | snp | A/C | 3.30497e-05 | 0.00406494 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067693 | AAACTTGTACACGAG[A/C]ATCTGAAATTAAATC | 672 |
rs748812609 | snp | A/C/G | 9.88517e-05 | 0.00702966 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094071 | ATCTGTGGCTCAGTA[A/C/G]CAAATGCTCCTATAA | 672 |
rs748836343 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113641 | CAAAGTGCTGGTATT[A/G]TAGGCGTGAGCCACC | 672 |
rs748839289 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082469 | GAGTCACTTATGATG[A/G]AAGGGTAGCTGTTAG | 672 |
rs748876625 | snp | C/G | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104122 | AACAAATGGTTTTAC[C/G]AAGGAAGGATTTTCG | 672 |
rs748894760 | snp | C/G/T | 1.65105e-05 | 0.00287315 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092173 | AGAAATCTGTATTAA[C/G/T]AGTCTGAACTACTTC | 672 |
rs748914651 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083734 | TTAAAATAATGAGTT[A/C]TTTTTGCTTATGGGC | 672 |
rs748923729 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099854 | AGTTCCAAGGTTAGA[C/G]AGTTGGACACTGAGA | 672 |
rs748960767 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046687 | TTAAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 672 |
rs748961672 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114940 | AAGATCATCAAATAC[A/G]TAAATATAACTTGAA | 672 |
rs748966067 | snp | A/C | 2.12276e-05 | 0.00325781 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095800 | CAGTACTGTATCTAC[A/C]CACTCTCTTTTCAGT | 672 |
rs748968240 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089735 | AAAAAATAGGCCAGG[C/T]GTGGTTGCACACACC | 672 |
rs748971390 | snp | A/G | 1.65479e-05 | 0.0028764 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082378 | AATTTTGCTTAAGAT[A/G]TCAGTGTTTGGCCAA | 672 |
rs749006434 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081908 | TGTTCTTTTCTTTTC[C/T]TTTTGAACTAACAGG | 672 |
rs749006461 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099348 | CGATCTCGGTTCACC[A/G]CAACCTCCACCTCCC | 672 |
rs749009072 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126267 | CGTCGACGCAATCGC[C/T]ACCAGTCAATGGGGT | 672 |
rs749134086 | snp | A/C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051914 | TGCTGGGATTACAGG[A/C/G]ATAAGCCACTGCGCC | 672 |
rs749140203 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080820 | ATAAGGTGAGGCTCA[C/G]GTCGGGGAGGATGGC | 672 |
rs749169255 | snp | G/T | 1.6495e-05 | 0.0028718 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045854 | TTCATTCTCCTGGAC[G/T]AGGCTCTAATCAATC | 672 |
rs749201522 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075015 | AAGAAAGGAAAGAAA[-/G]GAAAGAAAGAAGGAA | 672 |
rs749204113 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058915 | AGAAACAATTCTGAC[A/T]GAAACTCAGATTGTA | 672 |
rs749278649 | in-del | -/ACACAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052781 | GACAGACGGACAGAA[-/ACACAC]ACACACACACACACA | 672 |
rs749290001 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045775 | CACTCTCGGGTCACC[A/G]CAGGTGCCTCACACA | 672 |
rs749294233 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073375 | AACAGCAGAGATGTC[A/G]TCCTTGAAACATTTC | 672 |
rs749319480 | snp | A/C | 1.66239e-05 | 0.00288299 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063884 | CTTACAGAAATAGCT[A/C]ACTACCCATTTTCCT | 672 |
rs749322383 | snp | A/C | 0.000103075 | 0.00717822 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104310 | GTTAGAGAAAAATGT[A/C]TGAATTATAATCAAA | 672 |
rs749348285 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117951 | AAAGCCTGCTCTCAT[A/T]GAGCTCATATTCTAG | 672 |
rs749377369 | snp | C/G | 0.000186724 | 0.0096606 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044785 | CAGACTTTTAGAAAT[C/G]TCTTCTAGTTTCATT | 672 |
rs749410065 | in-del | -/T | 0.399819 | 0.200136 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044804 | CTAGTTTCATTTTCC[-/T]TTTTTTTTTTTTTTT | 672 |
rs749415463 | snp | C/T | 1.65184e-05 | 0.00287384 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093740 | ATTGTGGATATTTAA[C/T]TCGAGTTCCATATTG | 672 |
rs749417532 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092368 | CATTAATACTGGAGC[C/T]CACTTCATTAGTACT | 672 |
rs749465132 | snp | A/C | 1.66668e-05 | 0.00288672 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063371 | TAATAGACTGGGTCA[A/C]CCCTAAAGAGATCAT | 672 |
rs749508254 | in-del | -/G | 1.6475e-05 | 0.00287006 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094492 | CTTTTCTCTCACACA[-/G]GGGATCAGCATTCAG | 672 |
rs749509905 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050485 | GGGCGTGGTGGCACA[C/T]GCCTGTAGTCTCAGC | 672 |
rs749522068 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076559 | CTTGTCAGCAGAAAG[A/G]CCTTCTGGATTCTGG | 672 |
rs749542853 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064721 | AACTGCTACAAAAGC[C/T]GATTTAGTAACATTT | 672 |
rs749592268 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103007 | CCCAAGCTGGGCTCA[A/C]AGGACCTCCTACCTC | 672 |
rs749593365 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094638 | TCAGCCTTTTCTACA[C/T]TCATTCTGTCTTTAG | 672 |
rs749609930 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071117 | TTGGGGAACTTTCAA[C/T]GCAGAGGTTGAAGAT | 672 |
rs749619044 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055555 | TTTGGGAGCCTGAGG[C/T]GGGCAGATGATCTGA | 672 |
rs749620949 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110053 | GTGCCCGCTACCACG[A/C]CTGGCTAACTTTTTG | 672 |
rs749649759 | in-del | -/AAAAG | 0.00040707 | 0.0142608 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104077 | AAAAAAAAGAAAAAA[-/AAAAG]AAAAGAAGAAGAAGA | 672 |
rs749668287 | in-del | -/AGAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063437 | TCTTTTCACGGAGAT[-/AGAG]AGGTCAGCGATTCAC | 672 |
rs749669760 | in-del | G/TGGAGTGCAGT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064878 | CTCTGTCAGCCAGGC[G/TGGAGTGCAGT]GGCTGGATCTCAGCT | 672 |
rs749670546 | snp | A/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124809 | TCGCCCAGGCTGGAG[A/T]GCAATGGCGCGATCT | 672 |
rs749675825 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108804 | TCAAGACCAGCCTGA[C/T]CAACACGGAGAAACC | 672 |
rs749702730 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071118 | TGGGGAACTTTCAAT[A/G]CAGAGGTTGAAGATG | 672 |
rs749737881 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43078698 | TTTCCTGAGTTAGTC[C/T]TCAAATGCATTATTT | 672 |
rs749750694 | snp | C/T | 3.20765e-05 | 0.00400465 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091342 | TCCTTTAACTATACT[C/T]GGAAATTTGTAAAAT | 672 |
rs749764532 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056831 | GGAATCCAAATTACA[C/T]AGCCTCTCTAAATCT | 672 |
rs749770970 | in-del | -/AAAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057837 | CGAGACTCCGTCTCA[-/AAAC]AAACAAACAAACAAA | 672 |
rs749784891 | snp | G/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126625 | TCTGAGGGACCGAGT[G/T]GGCGAAAAGCGCCGG | 672 |
rs749792136 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095094 | CAGAATTTTCCCTAT[G/T]CAGAAACCACACCTA | 672 |
rs749875230 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103845 | GGCACAGTGGCTCAC[A/C]CCTGTAATCCCAGCA | 672 |
rs749878880 | in-del | -/T | 1.69983e-05 | 0.00291528 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097332 | TCAATAAAAGTTTTC[-/T]TAATTAAAAGGGTTA | 672 |
rs749896277 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093583 | ACTTTTTTTTCTTTA[C/T]CTCTTCACTGCTAGA | 672 |
rs749910868 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090849 | GCCATTAATTCAAAG[A/C]GATGATGTCAGCAAA | 672 |
rs749918224 | snp | C/G | 1.64727e-05 | 0.00286986 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057035 | GATTTTTGTCAACTT[C/G]AGGGAGGGAGCTTTA | 672 |
rs750040616 | snp | A/G/T | 1.65982e-05 | 0.00288077 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43051115 | TTCTAGCCCCCTGAA[A/G/T]ATCTGGAAGAAGAGA | 672 |
rs750041297 | in-del | -/A | 0.000117024 | 0.00764841 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104105 | AAGAAGAAGAAGAAG[-/A]AAACAAATGGTTTTA | 672 |
rs750065093 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123339 | CCTCTCAACGACACC[C/G]ATCATCCATGTTTTT | 672 |
rs750095985 | snp | C/T | 3.30093e-05 | 0.00406246 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074320 | TTCCAATACAGCAGA[C/T]GAAATATTACCTAGA | 672 |
rs750107618 | snp | A/C | 1.64749e-05 | 0.00287005 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091577 | TTGTTTGGAAGAACC[A/C]ATCAAGAAAGGATCC | 672 |
rs750113197 | snp | C/T | 3.3089e-05 | 0.00406736 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43091916 | CTCTAATTTCTTGGC[C/T]CCTCTTCGGTAACCC | 672 |
rs750116574 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085284 | AAGAATCACTTGAAC[A/C]CAGGTGGCGGAAGTG | 672 |
rs750185403 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081049 | GCATTTCAGTTACAG[A/G]TCTCCAGAAAAAAAT | 672 |
rs750275408 | snp | C/T | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104237 | GAGTTATTTTCCTTT[C/T]TTGCAAAATTATAGC | 672 |
rs750344093 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082574 | TGCATGGTATCCCTC[C/T]GCTTCAAAAACGATA | 672 |
rs750353662 | snp | A/G | 1.65075e-05 | 0.00287289 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104108 | AAGAAGAAGAAGAAA[A/G]CAAATGGTTTTACCA | 672 |
rs750362244 | in-del | AGGTCCAGGCCGGGC/GGTCCAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121087 | CACCCCGAAAAAAAA[AGGTCCAGGCCGGGC/GGTCCAG]GCAGTGGCTCAGGAC | 672 |
rs750367794 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120630 | ATTAGCCGGGCGTGG[C/T]GGTGGACGCCTGTAG | 672 |
rs750368091 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065962 | TTTATGTATCTTTAC[C/T]ATCTACCTCTGGATA | 672 |
rs750396716 | snp | A/C | 1.6476e-05 | 0.00287014 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057167 | ACAACCCATCAGGAT[A/C]AGAGAAAGAGAAGCT | 672 |
rs750436562 | in-del | -/CACACT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052820 | ACACACACACACACA[-/CACACT]CTCTTACTTTACCGC | 672 |
rs750437234 | snp | G/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076545 | GCAGACACCTCAAAC[G/T]TGTCAGCAGAAAGGC | 672 |
rs750463455 | snp | A/C | 7.56888e-05 | 0.00615131 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124146 | AAAACATATATATAT[A/C]TCTTTTTAAAAGGTT | 672 |
rs750547789 | in-del | -/AACTA | 0.000501484 | 0.0158269 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091333 | AGAAGCAGTTCCTTT[-/AACTA]TACTTGGAAATTTGT | 672 |
rs750565541 | snp | A/G | 4.94849e-05 | 0.00497393 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047735 | GAAAGAGCATTCAAA[A/G]TGTCAAAGTAGGACT | 672 |
rs750570405 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056590 | GTCAGGGGTTCAAGA[A/C]CAGCCTGGGCAAGAT | 672 |
rs750577818 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079621 | CAGCTTCCTGAAACG[C/G]GTGAAGGAAAATGAT | 672 |
rs750594744 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093170 | CCCTAGAGTGCTAAC[C/T]TCCAGTAACGAGATA | 672 |
rs750645074 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093039 | TCATGTCCCAATGGA[C/T]ACTTAAAGCCTTCTG | 672 |
rs750646315 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058317 | AGTTGGAGGCTGCAG[C/T]GAACTGTGATCATAC | 672 |
rs750701163 | snp | C/T | 1.64914e-05 | 0.00287149 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045849 | GTCAATTCATTCTCC[C/T]GGACTAGGCTCTAAT | 672 |
rs750704225 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074670 | GCAAGACAGCCTAGA[A/G]GTCTGGATTCATGTT | 672 |
rs750718476 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071060 | AGCAGTATCAGTAGT[A/G]TGAGCAGCAGCTGGA | 672 |
rs750718896 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101710 | TTTCACCATGTTGGC[C/T]AGGCTGGTCTCAAAC | 672 |
rs750724357 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112486 | GGCAAATGCCATGTA[C/T]CTGTAGTCCTAGCTA | 672 |
rs750745377 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085840 | TCACATTCATTACAT[A/G]TAAATATATATATAA | 672 |
rs750770955 | snp | G/T | 3.44501e-05 | 0.00415016 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063978 | AAAACACTCAAAGGA[G/T]TAGAAGTTGAAAACA | 672 |
rs750795452 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047935 | TACCACCACCCCTGG[A/C]TAATTTTTTTGTATT | 672 |
rs750825948 | snp | C/T | 7.27365e-05 | 0.00603017 | intron-variant, missense | BRCA1 | GRCh38.p7 | 17:43079387 | TTGTTCCTTTGGCCA[C/T]GTATATGCGAATCTG | 672 |
rs750834940 | snp | C/G | 0.000185237 | 0.00962206 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045358 | AGCCAACAACAGCCT[C/G]AATAGAAAGAATAGG | 672 |
rs750905289 | snp | C/T | 1.69456e-05 | 0.00291075 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063859 | GGAGGAGGGGAGAAA[C/T]AGTATTATACTTACA | 672 |
rs750927265 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089148 | TGAAACCCTCTCTCT[A/G]CTAAAAAAATACAAA | 672 |
rs750938749 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071054 | ATACCCAGCAGTATC[A/G]GTAGTATGAGCAGCA | 672 |
rs750964493 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049636 | GTAATTACTGTAAAT[A/G]TCAAGAGATGGGAAG | 672 |
rs750994654 | snp | A/C | 1.65091e-05 | 0.00287303 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076658 | CTTTACTGCTTTGTT[A/C]TGATAGTGATAATTC | 672 |
rs751024808 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073766 | TATATATATATATAT[-/A]TTTTTTGAGATGGAG | 672 |
rs751037790 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124738 | CCTCTCATACATACC[A/G]GCCGGTGTTTTTTGT | 672 |
rs751058529 | snp | G/T | 1.65798e-05 | 0.00287917 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074304 | AAAATCAAAGTGTTT[G/T]TTCCAATACAGCAGA | 672 |
rs751076235 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050237 | CACCAAGGCCTTTGT[A/G]CTGCGCAACTCCAGA | 672 |
rs751078452 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104153 | GGTTCACTCTGTAGA[A/G]GTCTTTTGGCACGGT | 672 |
rs751091558 | in-del | -/GCAAAA | 1.6501e-05 | 0.00287232 | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104240 | TTATTTTCCTTTTTT[-/GCAAAA]TTATAGCTGTTTGCA | 672 |
rs751104940 | snp | A/G | 3.29995e-05 | 0.00406185 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093360 | TCTCTTGGAAGGCTA[A/G]GATTGACAAATTCTT | 672 |
rs751124745 | snp | A/C/T | 3.29506e-05 | 0.00405884 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094617 | TGTTTGCTTTTATTA[A/C/T]AGAATTCAGCCTTTT | 672 |
rs751126600 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065495 | CTGACATGGAAAAAC[C/G]CTGTCTCTACTAAAA | 672 |
rs751137579 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090741 | TGTAGGCTGTGTGTG[C/T]GCGTGTGCGTGTGTG | 672 |
rs751162129 | snp | C/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126105 | CAAGTAGTCTTGTAA[C/G]GTCAGTGGCCTGCGG | 672 |
rs751190043 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073116 | GTAGGAAGATTGCAT[A/G]AGGCCAGGAGTTAGA | 672 |
rs751226166 | snp | A/C/T | 0.000502403 | 0.0158421 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091335 | AAGCAGTTCCTTTAA[A/C/T]TATACTTGGAAATTT | 672 |
rs751253440 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051385 | TGTCATTCAAGGACT[A/G]AGCATCTCACTTTTG | 672 |
rs751259743 | in-del | -/GAT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059616 | TCTAATTTAATATTA[-/GAT]CTAACAAGATCTATT | 672 |
rs751279771 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089461 | CATTATCAAATGGTC[A/C]TATATATGGTAAAGC | 672 |
rs751293910 | snp | A/G | 0.000561026 | 0.0167391 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104077 | AAAAAAAAGAAAAAA[A/G]AAAGAAAAGAAGAAG | 672 |
rs751327778 | snp | A/C | 1.64909e-05 | 0.00287144 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045580 | TAGCCAGGACAGTAG[A/C]AGGACTGAAGAGTGA | 672 |
rs751368643 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092256 | CTTTGTTTATAGACC[C/T]CAGGTTGCAAAACCC | 672 |
rs751446170 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064199 | ATCTGTCCACTCCCT[A/C]TTCTCAACACCCATC | 672 |
rs751508212 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079474 | CCCACAAGTGTTACC[A/G]TGGCAAAACTGGAAA | 672 |
rs751542189 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087226 | ATATTTAGCTATCAG[A/G]ATGCCACTATAGTGA | 672 |
rs751548030 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124376 | TCCAAGAAAGAGAAA[A/G]CTACAGAGGAGTGAC | 672 |
rs751653743 | snp | A/G | 1.64798e-05 | 0.00287047 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045814 | ATTGCTGGAGACAGA[A/G]AACACAAGCAGAGAT | 672 |
rs751656678 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093028 | TGTGGTTAACTTCAT[A/G]TCCCAATGGATACTT | 672 |
rs751690840 | snp | A/T | 1.65004e-05 | 0.00287227 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094274 | ACCAGAATATTCATC[A/T]ACCTCATTTAGAACG | 672 |
rs751693860 | snp | C/T | 1.64781e-05 | 0.00287033 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070909 | TAGTCATTAGGGAGA[C/T]ACATATGGATACACT | 672 |
rs751755637 | in-del | -/TAT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059901 | GCTACACTGGCCTAT[-/TAT]TATTATTATTATTAT | 672 |
rs751773452 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109295 | AGCCATCAAGCCTGG[A/C]CTTATCTTCATTTTT | 672 |
rs751802056 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098148 | ACTCACCTCTGCCTC[C/G]TGAGTAGCTGGGACT | 672 |
rs751814703 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056407 | TGGTATCGAACTCCT[C/T]GGCTCAAGCGATCTG | 672 |
rs751852694 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125797 | TAATAAGGATTGTTG[A/G]GGGGGTGGAGGGAAA | 672 |
rs751856943 | snp | A/G | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067675 | GATGTGGTGTTTTCT[A/G]GCAAACTTGTACACG | 672 |
rs751882850 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115885 | TGAGCTGTTATGACT[A/G]AGTCAACATAAGGCC | 672 |
rs751915222 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060994 | TCGGGTGTGGTAGCA[C/T]GCGTGCCTGTAATAC | 672 |
rs751937881 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114308 | AACATACAGTTCATT[C/T]CAGAAAGATTCTCAT | 672 |
rs752050539 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047578 | CTCAAGCACCAGGTA[A/T]TGAGTGATAAACCAA | 672 |
rs752088834 | snp | C/T | 3.57079e-05 | 0.00422524 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106443 | AACCTAGCATCATTA[C/T]CAAATTATATACCTT | 672 |
rs752097677 | in-del | -/ATATATATATGTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100621 | TAACATATATATAAC[-/ATATATATATGTT]ATATATATATAACAT | 672 |
rs752122039 | snp | C/G | 3.29511e-05 | 0.00405887 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091775 | CTCTGTGTTCTTAGA[C/G]AGACACTCGGTAGCA | 672 |
rs752140674 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062254 | GCACACTGCCATGCC[C/T]GGCTAATTAAAAAAA | 672 |
rs752155138 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046702 | GGAGGTTGCAGTGAG[C/T]CAAGACTGGGCCACT | 672 |
rs752164835 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100229 | ATTTTTTTTTCTGTT[A/G]TCTTAAATTTTTCAA | 672 |
rs752171726 | snp | G/T | 6.09812e-05 | 0.00552149 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091309 | TAGGAGGAACATGTT[G/T]CAAGTTTAAGAAGCA | 672 |
rs752198747 | snp | A/C/T | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094488 | CATTCTTTTCTCTCA[A/C/T]ACAGGGGATCAGCAT | 672 |
rs752199267 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062824 | CTGATCTCGAACTCC[C/T]GAGCTCAGGCAATCT | 672 |
rs752211002 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117566 | CAACACAGTGAAACG[C/T]TGTCTCTACTAAAAA | 672 |
rs752284897 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103776 | TCACTAACATATTCA[A/C]AATGCTCAATAAAGA | 672 |
rs752300203 | snp | C/T | 2.13158e-05 | 0.00326458 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090961 | GAGTGGTTAAAATGT[C/T]ACTCTGAGAGGATAG | 672 |
rs752318742 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087665 | GAAACTCCATCTCAG[A/G]AAAAAAAAAAAAAAA | 672 |
rs752366485 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096642 | ACATAGTTGGGGTTG[C/T]TTGTAGTTTATTATA | 672 |
rs752382877 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049907 | TCTGTCTGACTGAAC[A/G]AAGGTTGACTAACTC | 672 |
rs752437850 | snp | A/G | 1.75681e-05 | 0.00296373 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063833 | AAAAATGCAATTCTG[A/G]GGTGTTAAAGGGAGG | 672 |
rs752440950 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101935 | TTAAAAGATAGGGTC[G/T]CAGTCACCTGCGCTG | 672 |
rs752442071 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118282 | GTAATAATCCAGGAG[A/G]ATATTGTAGGGAAAG | 672 |
rs752474843 | in-del | -/TC | 1.65083e-05 | 0.00287296 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093691 | GCCTGGTAGAAGACT[-/TC]CTCCTCAGCCTATTC | 672 |
rs752541407 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113913 | AACCCTGTCTCGACT[A/C]AAAATACAAAAATTA | 672 |
rs752555905 | snp | C/G | 0.000927558 | 0.0215155 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125167 | GTTCCGCCCCTACCC[C/G]CCGTCAAAGAATACC | 672 |
rs752584874 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123236 | TATATAAAAAAAAAA[-/C]CTCTGCATTTCATTG | 672 |
rs752624544 | snp | C/T | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071166 | GCTGACTCTGGGGCT[C/T]TGTCTTCAGAAGGAT | 672 |
rs752640996 | snp | A/G | 1.71015e-05 | 0.00292411 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071280 | TACACAACGATGAAT[A/G]TTGAATTACAAAGTT | 672 |
rs752666233 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117154 | TTTAGAAAATGATAA[G/T]CTTAAGGCCGGGCAT | 672 |
rs752715574 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094597 | GGCTCCTTGCTAAGC[A/C]AGGCTGTTTGCTTTT | 672 |
rs752781278 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082744 | CATTCATGCAATTAA[C/T]GCCCATGAAATTATT | 672 |
rs752808917 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094115 | TACATGGCTTAAGTT[A/G]GGGAGGCTTGCCTTC | 672 |
rs752811560 | snp | G/T | 0.000109439 | 0.00739646 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045545 | AGTCCTTTTCAGGCT[G/T]ATGTACATAAAATAT | 672 |
rs752813317 | snp | C/T | 4.94262e-05 | 0.00497098 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099920 | CAAGCAATTGTTGGC[C/T]AGTTCTGTGCTTTTC | 672 |
rs752824502 | snp | A/G | 3.29538e-05 | 0.00405904 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082429 | TGTGCTTTGTTCTGG[A/G]TTTCGCAGGTCCTCA | 672 |
rs752848219 | snp | A/C | 1.6612e-05 | 0.00288196 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067580 | TATGCAGCAGATGCA[A/C]GGTATTCTGTAAAGG | 672 |
rs752875919 | snp | C/T | 1.6504e-05 | 0.00287258 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092129 | ACTTCCCATAGGCTG[C/T]TCTAAGTTATCTGAA | 672 |
rs752898474 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122726 | CCAGCATGGCCAACA[C/T]AGCAAAACCCTATCT | 672 |
rs752899392 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107981 | GGTGAAGGGGGTGAC[C/T]AGGTAGGGAGTAAAT | 672 |
rs752940034 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099806 | AGACGTCTTTTGAGG[C/T]TGTATCCGCTGCTTT | 672 |
rs752947940 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124255 | AAAGAACTAATGACA[A/G]CGTCCTTTATTTTTA | 672 |
rs752951392 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074117 | ATCATTAGTTAAACC[A/G]TTAATTAAAATATAG | 672 |
rs752961329 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069157 | TAGAGAAGCTAATGA[C/T]ATCCTCCCCCTTTTG | 672 |
rs752995539 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102346 | AAAGTGCTGGGATTA[C/T]AGGCGTGAAGCTTTT | 672 |
rs753063800 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105134 | GCAGTGATTTAGTAA[C/G]TTTTTGTCATTCATT | 672 |
rs753081589 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091751 | ATTCTTCAATGATAA[C/T]AAATTCTCCTCTGTG | 672 |
rs753099787 | snp | A/C | 1.65239e-05 | 0.00287431 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094719 | GTGCCACATGGCTCC[A/C]CATGCAAGTTTGAAA | 672 |
rs753135913 | in-del | -/TTAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43061435 | AATCCTACCAGGGAC[-/TTAG]TTAGTCTTATTTACT | 672 |
rs753156283 | in-del | -/C | 6.7149e-05 | 0.00579396 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049244 | AATCTGCATACTTAA[-/C]CCCAGGCCCTCTACC | 672 |
rs753175231 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071732 | TTATGGGCCGAGCAC[A/G]GTGGCTCACACCTGT | 672 |
rs753210219 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091595 | CAAGAAAGGATCCTG[A/G]GTGTTTGTATTTGCA | 672 |
rs753221582 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097598 | GTTTCTACTGAAAAC[A/G]AAAACAAAAACAAAA | 672 |
rs753256448 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092923 | GATTTGAAAACGGAG[C/T]AAATGACTGGCGCTT | 672 |
rs753270719 | snp | C/G | 0.00015252 | 0.00873138 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110614 | AAAAAAGTAGCTGTT[C/G]AAAAATTTAAGTTAC | 672 |
rs753286589 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092445 | TTTTCTCTAATGTTA[C/T]TACGGCTAATTGTGC | 672 |
rs753293205 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114159 | TACAGCTTCGAACTC[C/T]TGGCCTTAAGTGATC | 672 |
rs753342801 | snp | G/T | 1.65375e-05 | 0.0028755 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104253 | TTGCAAAATTATAGC[G/T]GTTTGCATCTGTAAA | 672 |
rs753346094 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100825 | CAACCTCCACCTCCC[A/T]GGTTCAGTTGATTCT | 672 |
rs753350860 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075845 | TCTAAATGTTTTCTG[C/G]CTTTGGGAGGGCAAG | 672 |
rs753440254 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092289 | AATCTAAGCATAGCA[C/T]TCAATTTTGGCCCTC | 672 |
rs753466164 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100486 | AGCTGGGTCTACAAG[C/T]GTGTGCAACTATGCC | 672 |
rs753487581 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057184 | GAGAAAGAGAAGCTT[C/T]CTTCAATGGAAGTGG | 672 |
rs753521391 | snp | A/T | 1.64852e-05 | 0.00287094 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093601 | CTTCACTGCTAGAAC[A/T]ACTATCAATTTGCAA | 672 |
rs753524038 | in-del | -/A | 1.65255e-05 | 0.00287445 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093880 | ATTCTCATGACCACT[-/A]ATTAGTAATATTCAT | 672 |
rs753549438 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43061279 | CAATTTTTTCAGAAA[C/G]GCTTTCCCTGGCCTC | 672 |
rs753568708 | in-del | -/TTC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090259 | CCTGCAGTAGGCATA[-/TTC]TTAAAATGGAGCTAT | 672 |
rs753588964 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122043 | TTTTCAATAAATTGA[C/T]AAATTGTGAATCCTG | 672 |
rs753624573 | in-del | -/TCTT | 3.30044e-05 | 0.00406216 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097232 | CATAGACAAAGGTTC[-/TCTT]TGACTCACCTGCAAT | 672 |
rs753629344 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106190 | CAGACAATGGGGGCA[C/T]GGCGATACAGCCCTA | 672 |
rs753642272 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120769 | GACTCCGTCTCAAAA[A/C]CAAAACAAACAAAAA | 672 |
rs753651115 | snp | A/G | 1.64833e-05 | 0.00287078 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43071150 | TATGTTGCCAACACG[A/G]GCTGACTCTGGGGCT | 672 |
rs753717081 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054373 | CCAAAGCAGTTTTCC[A/T]TAGGAAATTACCTCT | 672 |
rs753735698 | snp | C/G | 4.55633e-05 | 0.00477279 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090950 | GCTTTTTACCTGAGT[C/G]GTTAAAATGTCACTC | 672 |
rs753745472 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084704 | CTTCACAAAGGTTTC[C/T]ACTGCTACTCTAACA | 672 |
rs753748171 | snp | C/G | 1.64944e-05 | 0.00287175 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094321 | CTTTGGCATTTGATT[C/G]AGACTCCCCATCATG | 672 |
rs753783953 | snp | A/G | 0.000186341 | 0.00965069 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045057 | GATCTGCCCACCTTG[A/G]CCTCCCAAAGTGCTG | 672 |
rs753793287 | in-del | -/C | 1.67455e-05 | 0.00289352 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063322 | GTTAGTTTGTAACAT[-/C]AAGTACTTACCTCAT | 672 |
rs753806745 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43053322 | TAGGAATGTTTATAT[C/G]CAGGCTAACACTCAG | 672 |
rs753859240 | snp | A/G | 4.94605e-05 | 0.0049727 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104862 | CTTGGGATATTCAAC[A/G]CTTACACTCCAAACC | 672 |
rs753888336 | snp | C/T | 0.000235924 | 0.0108585 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079403 | GTATATGCGAATCTG[C/T]AAGAAAGGTGAAATT | 672 |
rs753931082 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096222 | TCTCTACTAAAAATA[C/T]AAAAATTAGCCGGGT | 672 |
rs753940026 | snp | C/G | 1.6473e-05 | 0.00286988 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43099792 | AATTCAATGTAGACA[C/G]ACGTCTTTTGAGGTT | 672 |
rs753960590 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059580 | TTCCCACTCCCCCAT[A/G]TTCCCTACCATGCCT | 672 |
rs754006900 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066020 | GTTAAAAACCAAGCA[C/T]GGTGCTTAAAACTGA | 672 |
rs754014157 | snp | A/G | 4.97492e-05 | 0.0049872 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091957 | GTGTATGGGTGAAAG[A/G]GCTAGGACTCCTGCT | 672 |
rs754014482 | snp | A/C | 1.86079e-05 | 0.00305018 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079287 | AGAACCACCATCTTT[A/C]AGTAATTTGCCAAAA | 672 |
rs754021358 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081421 | AAGCCACTGTTCTGT[A/G]TAAGTAGCAGACTTG | 672 |
rs754031447 | snp | A/G | 1.79332e-05 | 0.00299437 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124157 | ATATATCTTTTTAAA[A/G]GGTTTATAAAATGAC | 672 |
rs754146940 | snp | A/G | 0.000216661 | 0.0104059 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110548 | CCTCATGATCGCACC[A/G]CTGTACTCCAGCTGG | 672 |
rs754152768 | snp | A/G | 1.65282e-05 | 0.00287469 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43049193 | CATCCATTCCAGTTG[A/G]TCTAAAATGGACATT | 672 |
rs754161909 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070502 | AAAACAAACACTAGA[-/G]GAAATGCTACTATCT | 672 |
rs754176240 | in-del | -/TGTAGA | 2.35098e-05 | 0.00342846 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106579 | TAATTTACTTCCTTT[-/TGTAGA]AAGAATACTCAAAAG | 672 |
rs754180847 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063793 | TCAGCATCAGCAAAA[-/A]CCTTAGGTGTTAAAC | 672 |
rs754222140 | snp | A/C/T | 1.64765e-05 | 0.00287019 | BRCA1 | 17 | allele_origin=T(germline)/A(germline) | 17:43092906 | CTCTTCTGCATTTCC[A/C/T]GGATTTGAAAACGGA | 672 |
rs754223780 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074177 | TAAACCTTGATTAAC[A/G]CTTGAGCTATTTTTC | 672 |
rs754256578 | snp | C/T | 4.94572e-05 | 0.00497254 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067645 | AGTCTCTTCAGTAAT[C/T]AGATTAGTTAAAGTG | 672 |
rs754327493 | snp | A/C/T | 4.53968e-05 | 0.00476407 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045611 | GAGGAGCTCCCAGGG[A/C/T]CTGGAAAGGCCACTT | 672 |
rs754332942 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073917 | GCACTAGCACACCCA[A/G]TTAATTTTTTTGTAT | 672 |
rs754351346 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072781 | ATTGGTCAGGTTGGT[C/T]CTGAACTCCTGCCCT | 672 |
rs754381855 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112965 | TGCGCCTCCACGCCC[A/G]TCTAATTTTGTATTT | 672 |
rs754398271 | snp | A/C | 1.65433e-05 | 0.002876 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093964 | TCTTTTGAACTGCCA[A/C]ATCTGCTTTCTTGAT | 672 |
rs754407454 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127142 | CCTGAGCCTCCCCGA[C/T]GGGCACCGCCCCCTG | 672 |
rs754413406 | snp | G/T | 0.000104053 | 0.00721218 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063986 | CAAAGGATTAGAAGT[G/T]GAAAACAAAATCAGG | 672 |
rs754436738 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111592 | TTAGGGAGGCCAAGG[C/T]GGGCAGATCACGAGG | 672 |
rs754440635 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116326 | CCATCAACTCATGGC[C/G]AAGCTGTTTCACCCA | 672 |
rs754508083 | snp | G/T | 3.30814e-05 | 0.00406689 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082601 | GATAAATGGCACCAA[G/T]AAAATGAAATACTTT | 672 |
rs754547769 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075969 | TGGGTGGCGCATGCT[C/T]GTGGACCCAGCTACT | 672 |
rs754597283 | snp | A/G | 9.88777e-05 | 0.00703058 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092293 | TAAGCATAGCATTCA[A/G]TTTTGGCCCTCTGTT | 672 |
rs754657379 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047938 | CACCACCCCTGGCTA[A/C]TTTTTTTGTATTTTT | 672 |
rs754660020 | in-del | -/TATTAATATTAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059617 | CTAATTTAATATTAC[-/TATTAATATTAA]TAACAAGATCTATTG | 672 |
rs754663252 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43053614 | GGAGCTGGTAGTGAG[A/C]CGAGACGGCGCCACT | 672 |
rs754708958 | in-del | -/TCTA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102733 | CATAGCTCACTGTAG[-/TCTA]TCTACATCTCCTGGA | 672 |
rs754726354 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43091114 | TTTTCTTCTCATTGG[C/T]AGGACTGGATTTACT | 672 |
rs754745268 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062693 | ACCTCCACCTCCCGG[A/G]TTCAAGAGATTCTCC | 672 |
rs754747408 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046944 | TGGAAAAATGTATGT[A/G]ATATCTTAAGGAAAA | 672 |
rs754753105 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067349 | AACCTCCATCTCCCC[A/G]GTTCAAGTGATTCTC | 672 |
rs754763517 | snp | A/G | 3.33222e-05 | 0.00408167 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124091 | GCGAAGAGCAGATAA[A/G]TCCATTTCTTTCTGT | 672 |
rs754789567 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122389 | TAGGTCCCAAGTACC[A/G]TTCTAACTACTGAAC | 672 |
rs754792932 | in-del | -/ACTCAGACCA | 1.64773e-05 | 0.00287026 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091523 | AACCAATTCCTTGTC[-/ACTCAGACCA]ACTCCCTGGCTTTCA | 672 |
rs754810358 | in-del | -/TC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110416 | CATGGCGAAACCCCG[-/TC]TCTACAGAAAACACA | 672 |
rs754835712 | in-del | -/TA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073750 | AAATATATGTGTGTA[-/TA]TATATATATATATAT | 672 |
rs754884276 | snp | C/G | 1.67919e-05 | 0.00289753 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049100 | GTGTCCTCCCTCTCT[C/G]ACAGGGCACCCAATA | 672 |
rs754970915 | snp | C/T | 1.65482e-05 | 0.00287643 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093968 | TTGAACTGCCAAATC[C/T]GCTTTCTTGATAAAA | 672 |
rs754999111 | snp | A/T | 1.75922e-05 | 0.00296577 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063994 | TAGAAGTTGAAAACA[A/T]AATCAGGAAGTGCTG | 672 |
rs755070698 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059594 | TATTCCCTACCATGC[C/T]TTCTTCATCTAATTT | 672 |
rs755100009 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081470 | AAGAAAGGTCTTAAA[A/G]TTCCCAGTTGGACTG | 672 |
rs755116419 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096233 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGCGCG | 672 |
rs755118284 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080621 | ACCAACTTGGGCAAC[A/T]TAGGGAGACCTTGTC | 672 |
rs755119795 | snp | C/G | 1.81473e-05 | 0.0030122 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079406 | TATGCGAATCTGTAA[C/G]AAAGGTGAAATTGTA | 672 |
rs755122577 | snp | A/G | 1.65176e-05 | 0.00287376 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093829 | ATTCTATTGGGTTAG[A/G]ATTTTTCTCATTCTG | 672 |
rs755171693 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068554 | AGATTTCATGTCTTT[-/A]AAAAAAAAAAAAAGT | 672 |
rs755174729 | snp | C/T | 1.85844e-05 | 0.00304826 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079290 | ACCACCATCTTTCAG[C/T]AATTTGCCAAAATGA | 672 |
rs755209182 | snp | A/G | 1.65844e-05 | 0.00287957 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091962 | TGGGTGAAAGGGCTA[A/G]GACTCCTGCTAAGCT | 672 |
rs755221482 | snp | C/T | 3.33283e-05 | 0.00408204 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097304 | CCTAAAAAATTTCCC[C/T]CCAAAAAATAAATCA | 672 |
rs755261514 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050993 | CCCCATCGTGGGATC[C/T]TGCTTATAATACTCC | 672 |
rs755268261 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066092 | GGCTCTGGATCTGTA[C/G]TTCACTTGCTCCAGA | 672 |
rs755285181 | snp | A/C | 1.65192e-05 | 0.00287391 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094711 | GAGTATTTGTGCCAC[A/C]TGGCTCCACATGCAA | 672 |
rs755296152 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082696 | CCTAGTATGGAACTA[C/T]AAGTTCTAGCTGAAC | 672 |
rs755342376 | snp | G/T | 0.000216708 | 0.0104071 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110550 | TCATGATCGCACCAC[G/T]GTACTCCAGCTGGGA | 672 |
rs755347133 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114928 | ATTTCAAAAGACAAG[-/A]TCATCAAATACGTAA | 672 |
rs755370895 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071191 | AAGGATCAGATTCAG[A/G]GTCATCAGAGAAGAG | 672 |
rs755379641 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113099 | TGAGCCACCGTGCCC[A/G]GCCTCAACAGCTGTC | 672 |
rs755405321 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089273 | GGTTGCAGTGAGCCA[A/C]AATTGTGCCACTGCA | 672 |
rs755411080 | in-del | -/G | 0.000301553 | 0.0122754 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044390 | CTGCCCTTGCACACT[-/G]GGGGGGGCTAGGGAA | 672 |
rs755416208 | snp | A/G | 1.77858e-05 | 0.00298205 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091375 | GCTCCCCAAAAGCAT[A/G]AACATTTAGCTCACT | 672 |
rs755419454 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126059 | CTCTTTAGGGAGACT[A/G]CAATTCCCATCCAGC | 672 |
rs755427809 | snp | A/G | 0.00095451 | 0.0218253 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43045697 | TAGTGGCTGTGGGGG[A/G]TCTGGGGTATCAGGT | 672 |
rs755494771 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095297 | AATTAAAAGTAAAGG[A/G]CAGGCCAGGCACAGT | 672 |
rs755516286 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092774 | ATTAACTGTCTGTAC[A/G]GGCTTGATATTAGAC | 672 |
rs755548080 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058485 | CTTTTTGGTAGACCA[C/G]GTGAAATGACTAGGA | 672 |
rs755614810 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082454 | TCCTCAAGGGCAGAA[A/G]AGTCACTTATGATGG | 672 |
rs755699679 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114334 | CTCATCCAGATAAAT[C/T]GAAAGCCCCAGGGCT | 672 |
rs755706172 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093584 | CTTTTTTTTCTTTAT[C/T]TCTTCACTGCTAGAA | 672 |
rs755731300 | snp | A/C/T | 1.64798e-05 | 0.00287047 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43074461 | TCTATTCTGAAGACT[A/C/T]CCAGAGCAACTGTGC | 672 |
rs755789142 | in-del | -/TTGATTTTCTTCCTT | 1.64792e-05 | 0.00287042 | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092801 | AGACTCATTCTTTCC[-/TTGATTTTCTTCCTT]TTGTTCACATTCAAA | 672 |
rs755843861 | snp | A/G | 1.6492e-05 | 0.00287154 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045850 | TCAATTCATTCTCCT[A/G]GACTAGGCTCTAATC | 672 |
rs755845310 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065850 | GTTCCAGATAACAGT[C/T]CTCTTCCGGGTAACG | 672 |
rs755911812 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118559 | CCCAAAGTACTGGGA[C/T]TACAGGAGTGAGCCA | 672 |
rs755920262 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071062 | CAGTATCAGTAGTAT[A/G]AGCAGCAGCTGGACT | 672 |
rs755935459 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120658 | TAGTCCCAGCTACTT[A/G]GGGGGCCGAGGCAGG | 672 |
rs755937136 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064365 | AGTATTGTTGAAAAC[C/T]TAAATCTGAAATGTC | 672 |
rs755958670 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43078452 | GCTGGGATTATAGGC[A/G]TGAGCCACCATGCCT | 672 |
rs756027029 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43053140 | CTCAGGCTCCCAAAG[A/G]CAAGTCTGTTTGTTT | 672 |
rs756065301 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089634 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 672 |
rs756130118 | snp | A/G | 1.64942e-05 | 0.00287173 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104114 | AAGAAGAAAACAAAT[A/G]GTTTTACCAAGGAAG | 672 |
rs756211343 | snp | A/G | 3.30409e-05 | 0.0040644 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43093734 | TTTTGAATTGTGGAT[A/G]TTTAATTCGAGTTCC | 672 |
rs756281673 | snp | A/G | 3.29522e-05 | 0.00405894 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43076550 | CACCTCAAACTTGTC[A/G]GCAGAAAGGCCTTCT | 672 |
rs756327180 | snp | C/T | 2.532e-05 | 0.003558 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115819 | AGAAAATAAATGAGG[C/T]TCAATAATTTATTTA | 672 |
rs756361151 | snp | A/G | 1.65007e-05 | 0.00287229 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047737 | AAGAGCATTCAAAGT[A/G]TCAAAGTAGGACTAC | 672 |
rs756361569 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102439 | TCGGCTCACTGCAAC[C/T]TCCGACTCTCAGGTT | 672 |
rs756452253 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069696 | TTGTATCTACCAGGG[C/T]AGCCACAGCTTACTT | 672 |
rs756476834 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085928 | TACTACATAATAAGC[C/T]TAATCCAGATACAAG | 672 |
rs756499058 | snp | A/C/T | 1.64846e-05 | 0.0028709 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43104914 | AATGATTTTCAATAG[A/C/T]TCTTCAACAAGTTGA | 672 |
rs756518403 | snp | C/T | 0.000109997 | 0.00741528 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045593 | AGAAGGACTGAAGAG[C/T]GAGAGGAGCTCCCAG | 672 |
rs756557335 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43053666 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAGAAA | 672 |
rs756559408 | snp | C/T | 1.64974e-05 | 0.00287201 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092622 | TGTAAAAGTCCATGT[C/T]TATTTGGAGTAATGA | 672 |
rs756577139 | in-del | -/ATT | 5.01006e-05 | 0.00500478 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104283 | AATACAAGGGAAAAC[-/ATT]ATGTTTGCAGTTAGA | 672 |
rs756586490 | snp | C/T | 1.68869e-05 | 0.00290571 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063862 | GGAGGGGAGAAATAG[C/T]ATTATACTTACAGAA | 672 |
rs756608161 | snp | A/G | 0.000185168 | 0.00962028 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045359 | GCCAACAACAGCCTG[A/G]ATAGAAAGAATAGGG | 672 |
rs756729124 | snp | A/T | 1.64963e-05 | 0.00287192 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093362 | TCTTGGAAGGCTAGG[A/T]TTGACAAATTCTTTA | 672 |
rs756740766 | snp | A/C | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123762 | AGTGCAGAACCAATC[A/C]AGACAGAGTCCCTGT | 672 |
rs756748588 | snp | C/T | 4.94482e-05 | 0.00497209 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093453 | GGGAAAGTATCGCTG[C/T]CATGTCTTTTACTTG | 672 |
rs756859863 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094630 | TACAGAATTCAGCCT[C/T]TTCTACATTCATTCT | 672 |
rs756948486 | snp | C/T | 1.68533e-05 | 0.00290282 | missense, intron-variant | BRCA1 | GRCh38.p7 | 17:43106475 | TGGTTATATCATTCT[C/T]ACATAAAGGACACTG | 672 |
rs756987689 | snp | A/C | 1.64746e-05 | 0.00287002 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094510 | GATCAGCATTCAGAT[A/C]TACCTTTTTTTCTGT | 672 |
rs757003198 | snp | A/T | 3.84371e-05 | 0.00438373 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104087 | AAAAAAAAAGAAAAG[A/T]AGAAGAAGAAGAAGA | 672 |
rs757024268 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080824 | GGTGAGGCTCAGGTC[A/G]GGGAGGATGGCTCAA | 672 |
rs757032165 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063116 | GCTGGTCTTGAACTC[C/T]CGACATCAGGTGATC | 672 |
rs757113004 | in-del | -/TGTG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100545 | ATATATACATATATA[-/TGTG]TGTGTGTGTGTATAT | 672 |
rs757144777 | in-del | -/TTTTT | 0.0737766 | 0.177328 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044805 | CTAGTTTCATTTTCC[-/TTTTT]TTTTTTTTTTTTTTG | 672 |
rs757146589 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052335 | ACTCAGGCTGGAGTA[C/T]AGTGGCACGATCATA | 672 |
rs757184166 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082440 | CTGGATTTCGCAGGT[C/T]CTCAAGGGCAGAAGA | 672 |
rs757215735 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091780 | TGTTCTTAGACAGAC[A/G]CTCGGTAGCAACGGT | 672 |
rs757237039 | snp | C/T | 1.65053e-05 | 0.0028727 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092141 | CTGTTCTAAGTTATC[C/T]GAAATCAGATATGGA | 672 |
rs757237381 | snp | C/G | 1.80847e-05 | 0.00300699 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079437 | GACATCAAGGGAACG[C/G]GTACTGTTCAAAAAG | 672 |
rs757310288 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069196 | CTCCGCCAGGATCAT[C/T]AGCAATTCTGAACTG | 672 |
rs757317633 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058391 | AAAAACACACACACA[C/T]ACACACATAAAACAA | 672 |
rs757333387 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108269 | GTTGAACCTGTGAGG[A/C]GGGGGTTACAGTGAG | 672 |
rs757383244 | snp | C/T | 3.29609e-05 | 0.00405948 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093030 | TGGTTAACTTCATGT[C/T]CCAATGGATACTTAA | 672 |
rs757415688 | snp | C/G | 0.000115391 | 0.00759487 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045832 | CACAAGCAGAGATTA[C/G]TGTCAATTCATTCTC | 672 |
rs757440752 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092943 | GACTGGCGCTTTGAA[A/G]CCTTGAATGTATTCT | 672 |
rs757442952 | snp | C/G | 0.000159764 | 0.00893623 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115796 | TAGCAGGGTAGGGGG[C/G]GAGAAAAAGAAAATA | 672 |
rs757465458 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124400 | GAGTGACTGACCGGG[C/T]AGGTGGTGGTAGCCT | 672 |
rs757494313 | snp | A/G | 1.92095e-05 | 0.0030991 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115690 | AGGACAAAAACAAAA[A/G]CTAATAATGGAGCCA | 672 |
rs757538941 | in-del | -/T | 1.70746e-05 | 0.00292182 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091293 | TCTATGAAAAGCACC[-/T]TAGGAGGAACATGTT | 672 |
rs757579891 | snp | C/T | 1.64811e-05 | 0.00287059 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092460 | TTACGGCTAATTGTG[C/T]TCACTGTACTTGGAA | 672 |
rs757612714 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100290 | GAAGTATTAATATAG[C/T]ATATTTTGAAGCTGA | 672 |
rs757629203 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098204 | TAATTTAAAAAAGAA[A/G]TTTTTTTGTAGAGAT | 672 |
rs757632961 | snp | C/T | 1.648e-05 | 0.0028705 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092313 | GGCCCTCTGTTTCTA[C/T]CTAGTTCTGCTTGAA | 672 |
rs757636586 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083528 | GCTCAGTTAATTAGA[C/T]AACTATTTACTATCT | 672 |
rs757657445 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093704 | CTTCCTCCTCAGCCT[A/G]TTCTTTTTAGGTGCT | 672 |
rs757665560 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43061052 | AATTGCTTGAACCCA[A/G]GAGACAGAGTTTGCA | 672 |
rs757676381 | snp | A/G | 0.000167546 | 0.00915123 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044393 | GCCCTTGCACACTGG[A/G]GGGGCTAGGGAAGAC | 672 |
rs757676453 | snp | A/G | 1.75118e-05 | 0.00295898 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063835 | AAATGCAATTCTGAG[A/G]TGTTAAAGGGAGGAG | 672 |
rs757726297 | snp | A/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076527 | TTACTGGTAGAACTA[A/T]CTGCAGACACCTCAA | 672 |
rs757728790 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126631 | GGACCGAGTGGGCGA[A/G]AAGCGCCGGAGAGTT | 672 |
rs757752898 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085428 | ACTTTTTGAACACTA[C/T]ATAATTGTTAGTCAT | 672 |
rs757781708 | snp | A/C | 1.82914e-05 | 0.00302413 | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43095923 | TCTTGATCTCCCACA[A/C]TATAGGGAAAAGACA | 672 |
rs757892853 | in-del | -/AG | 3.3129e-05 | 0.00406982 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099734 | TAAGATAAGGAATCC[-/AG]CAATTATTATTAAAT | 672 |
rs757933953 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093190 | GTAACGAGATACTTT[C/T]CTGAGTGCCATAATC | 672 |
rs757936216 | snp | C/T | 1.64749e-05 | 0.00287005 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094604 | TGCTAAGCCAGGCTG[C/T]TTGCTTTTATTACAG | 672 |
rs757949570 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116762 | GACCTCAGGTGATCC[A/G]CCTGCCTTGGCCTCC | 672 |
rs757955666 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062825 | TGATCTCGAACTCCT[A/G]AGCTCAGGCAATCTG | 672 |
rs757970615 | snp | A/G | 5.9261e-05 | 0.00544307 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091312 | GAGGAACATGTTTCA[A/G]GTTTAAGAAGCAGTT | 672 |
rs757971617 | snp | C/T | 1.64849e-05 | 0.00287092 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104908 | AGCACAAATGATTTT[C/T]AATAGCTCTTCAACA | 672 |
rs757987511 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094491 | TCTTTTCTCTCACAC[A/T]GGGGATCAGCATTCA | 672 |
rs757988169 | in-del | -/G | 1.86104e-05 | 0.00305038 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091371 | ATGTGCTCCCCAAAA[-/G]CATAAACATTTAGCT | 672 |
rs758001361 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117654 | TAAGGCAGGAGAATC[A/G]CTTGAACCGGGGAAG | 672 |
rs758010867 | snp | C/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123598 | CGTGATCCTACCACC[C/T]TGGCCTCCCAAAGTG | 672 |
rs758043813 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055986 | GAGCTAGACTTCCTG[-/A]GTTCAACTTCTAGTT | 672 |
rs758063472 | snp | G/T | 1.80984e-05 | 0.00300813 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079426 | GTGAAATTGTAGACA[G/T]CAAGGGAACGGGTAC | 672 |
rs758108974 | snp | A/G | 1.67086e-05 | 0.00289033 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104283 | AATACAAGGGAAAAC[A/G]TTATGTTTGCAGTTA | 672 |
rs758149063 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054614 | CCAATTAATTTTTAA[A/T]TTTTTTTGTAGAGAC | 672 |
rs758156788 | snp | A/G | 0.00018648 | 0.00965429 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045292 | AGAGAAGTAAACTTA[A/G]GGAAACCAGCTATTC | 672 |
rs758168859 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055013 | CCTTGGGCTCCCAAA[G/T]TGCTGGGATCACAGG | 672 |
rs758180755 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093064 | CTTCTGTGTCATTTC[C/T]ATTATCTTTGGAACA | 672 |
rs758189670 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049927 | TTGACTAACTCACCC[C/T]CAAAATAATACTTTC | 672 |
rs758204650 | in-del | -/AAGTTC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101896 | ACAATTACACCTTTT[-/AAGTTC]AAGTAATTTTCCCTT | 672 |
rs758215949 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109258 | TGCCTTGGCATCCCA[A/G]CGTGCTGGGATTACA | 672 |
rs758221694 | snp | G/T | 3.35216e-05 | 0.00409386 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097313 | TTTCCCCCCAAAAAA[G/T]AAATCAATAAAAGTT | 672 |
rs758295315 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059426 | TGAGATCGTGCTACC[A/G]CACTCCATGCACTCT | 672 |
rs758329415 | snp | C/G | 1.64923e-05 | 0.00287156 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091886 | ATCCTCACTAGATAA[C/G]TTCTCTTCTGAGGAC | 672 |
rs758407710 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43078015 | GATGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 672 |
rs758449088 | snp | G/T | 0.000149141 | 0.00863414 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045705 | GTGGGGGATCTGGGG[G/T]ATCAGGTAGGTGTCC | 672 |
rs758452509 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121049 | CACTCCAGCCTGGGC[A/G]ACAGAGCCAGACTCC | 672 |
rs758515222 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091484 | ATTTTCTTCCAAGCC[C/T]GTTCCTCTTTCTTCA | 672 |
rs758535463 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085221 | TTCTTCCATAAAGAC[C/G]CTTAGTGCTCCATCC | 672 |
rs758537599 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067404 | GGACTACAGGCGCAC[A/G]CGACCACACCCAGCT | 672 |
rs758539222 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067665 | TAGTTAAAGTGATGT[A/G]GTGTTTTCTGGCAAA | 672 |
rs758539310 | snp | A/C | 1.72136e-05 | 0.00293369 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045635 | GCCACTTTGTAAGCT[A/C]ATTCTTGGGGTCCTG | 672 |
rs758554027 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082799 | AAATCCTCAAATTCC[A/C]CCAAATAGACTTGAT | 672 |
rs758556342 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044750 | AGAACACATTCTTTA[A/G]AAATCTAGCAAATAT | 672 |
rs758598971 | snp | C/T | 3.3048e-05 | 0.00406484 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093877 | TTTTATTCTCATGAC[C/T]ACTATTAGTAATATT | 672 |
rs758603985 | in-del | -/TGTC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073718 | TGGCCTTTGGACTCT[-/TGTC]TAACAGTTGAAATAA | 672 |
rs758630283 | snp | G/T | 1.66123e-05 | 0.00288199 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067581 | ATGCAGCAGATGCAA[G/T]GTATTCTGTAAAGGT | 672 |
rs758689047 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114195 | GCCTTGGCCTCCCAA[A/C]GTGCTGGGGTTATGG | 672 |
rs758739620 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057055 | AGGGAGCTTTACCTT[C/T]CTGTCCTGGGATTCT | 672 |
rs758779691 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076491 | GATGTTTCTTACCTT[C/T]CCACTCCTGGTTCTT | 672 |
rs758780152 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047728 | CAGGAAGGAAAGAGC[A/T]TTCAAAGTGTCAAAG | 672 |
rs758790501 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096465 | TAGTCCCAGCTACTC[A/G]TGAGATTGAGACAGG | 672 |
rs758809074 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113394 | TTTTTTTCAGACAGA[C/G]TCTCACTCTGTTGTC | 672 |
rs758878834 | snp | A/G | 0.000501128 | 0.0158213 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110628 | TGAAAAATTTAAGTT[A/G]CATTTATTGCTCACA | 672 |
rs758892386 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097355 | AAGGGTTAAAAAAAT[G/T]TACTTGTTGAAAAAC | 672 |
rs758969201 | snp | A/C | | | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43043804 | ATCTAATCACTTGAG[A/C]CCTTAGAAACAGAGA | 672 |
rs759021873 | in-del | -/ACA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059472 | CGAGATGCTGTCACA[-/ACA]ACAACAACAACAACA | 672 |
rs759043094 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076328 | TAGGTTCAAAAAACC[C/T]ATATAGGATTAAACA | 672 |
rs759047220 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110189 | GTGAGCCACCGCACC[C/T]GGCCTCGAATCTTTC | 672 |
rs759063490 | in-del | -/C | 0.00259547 | 0.0359305 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125163 | CAGGTTCCGCCCCTA[-/C]CCCCCCGTCAAAGAA | 672 |
rs759108406 | snp | C/G | 1.65097e-05 | 0.00287308 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093796 | CTTTCGTTTTGAAAG[C/G]AGATTCTTTTTCGAG | 672 |
rs759143469 | snp | C/T | 3.52212e-05 | 0.00419635 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063823 | CGTTAGGTGTAAAAA[C/T]GCAATTCTGAGGTGT | 672 |
rs759148456 | in-del | -/AAAAAAGAAAAGAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104075 | AAAAAAAAAAGAAAA[-/AAAAAAGAAAAGAA]GAAGAAGAAGAAGAA | 672 |
rs759157605 | snp | C/T | 1.65113e-05 | 0.00287322 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093692 | CCTGGTAGAAGACTT[C/T]CTCCTCAGCCTATTC | 672 |
rs759168195 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117326 | GCATGCCTGTGGTCT[C/T]AGCTACTTTGGAGAC | 672 |
rs759197544 | snp | C/T | 1.65083e-05 | 0.00287296 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43097258 | CCTGCAATAAGTTGC[C/T]TTATTAACGGTATCT | 672 |
rs759293156 | snp | A/G | 4.94915e-05 | 0.00497426 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076642 | TGAGAAAACAAATCT[A/G]CTTTACTGCTTTGTT | 672 |
rs759311557 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068837 | TTCTCTCGTAAGAAG[G/T]CTTAGAAGGGGTTCA | 672 |
rs759314330 | snp | A/G | 6.59326e-05 | 0.00574125 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071151 | ATGTTGCCAACACGA[A/G]CTGACTCTGGGGCTC | 672 |
rs759344059 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086646 | AAAAACAAGGACATT[A/G]TATATTGAATGTCAA | 672 |
rs759352570 | snp | C/T | 1.68937e-05 | 0.0029063 | intron-variant | BRCA1 | GRCh38.p7 | 17:43071263 | ATGGGAGAAGTTTAA[C/T]TTACACAACGATGAA | 672 |
rs759366409 | snp | G/T | 1.64849e-05 | 0.00287092 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094667 | AGTGAGTAATAAACT[G/T]CTGTTCTCATGCTGT | 672 |
rs759369473 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056026 | ATTACCTGTGTGACT[C/T]TGAGCAACTTATTCA | 672 |
rs759414756 | snp | C/T | 6.87403e-05 | 0.0058622 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091282 | AAGGACTTTTTTCTA[C/T]GAAAAGCACCTTAGG | 672 |
rs759416378 | snp | C/T | 1.67868e-05 | 0.00289709 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045553 | TCAGGCTGATGTACA[C/T]AAAATATTTAGTAGC | 672 |
rs759417413 | snp | A/G | 0.00010982 | 0.0074093 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106536 | CAGCATGCAAAATCT[A/G]TAAATTATAAAGAAA | 672 |
rs759419385 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094580 | AGCCCATCTGTTATG[C/T]TGGCTCCTTGCTAAG | 672 |
rs759429870 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084670 | AGGAGGTTTTTATGA[C/T]CAGAAAATGTATTCC | 672 |
rs759457323 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070372 | TTAATGGGTATTTTT[C/T]CACAGTATGAAGCAA | 672 |
rs759508496 | snp | A/G | 3.8483e-05 | 0.00438634 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115684 | TTATGAAGGACAAAA[A/G]CAAAAGCTAATAATG | 672 |
rs759523510 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125395 | AGTCGCAGTTTTAAT[C/T]TATCTGTAATTCCCG | 672 |
rs759612271 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099892 | CCTGCTAAACAGTAT[A/G]GTAAAGAACAGTCAA | 672 |
rs759631547 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075226 | TTATGAAGATAGAAA[A/G]TTGATCAATGTCGAC | 672 |
rs759655692 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093414 | TTAGTAAAAGAACCA[A/G]GTGCATTTGTTAACT | 672 |
rs759679074 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097439 | AGTTAAGCTAGTATG[C/T]AATACAGAGAAGTGG | 672 |
rs759750310 | snp | A/G | 0.0003944 | 0.0140372 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125362 | CGTCCAGGAAGTCTC[A/G]GCGAGCTCACGCCGC | 672 |
rs759771021 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047357 | ACCTCCATCTTGACC[C/T]CCCAAAGTGCTGGAA | 672 |
rs759776172 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057004 | AAGGGGAGTGGAATA[C/T]AGAGTGGTGGGGTGA | 672 |
rs759777623 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052615 | ATGTTTTGGGTGACT[A/C]TCAGTGTCTTGACCT | 672 |
rs759802538 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090427 | CACCCAGGCTGGAGT[A/G]CAGTGGTACAATCCC | 672 |
rs759820303 | in-del | -/CTCT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083198 | TTTTTTTAAGTCTCC[-/CTCT]GTCACCCAGGTTGGC | 672 |
rs759853985 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105587 | CCAATCCCTCACTTA[C/G]TTCTGCCTCTCAAGG | 672 |
rs759867616 | snp | A/G | 3.31351e-05 | 0.00407019 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43051067 | CAGGCTCTTACCTGT[A/G]GGCATGTTGGTGAAG | 672 |
rs759877342 | in-del | -/ATATATATAACATATATATATATATATATATAAT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100647 | TTATATATATATAAC[lengthTooLong]ATATATATATATATA | 672 |
rs759878392 | snp | A/G | 1.64933e-05 | 0.00287165 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094222 | ATATTAAAGCCTCAT[A/G]AGGATCACTGGCCAG | 672 |
rs759882045 | snp | C/T | 1.6473e-05 | 0.00286988 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43099815 | TTGAGGTTGTATCCG[C/T]TGCTTTGTCCTCAGA | 672 |
rs759916956 | snp | A/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091590 | CCAATCAAGAAAGGA[A/T]CCTGGGTGTTTGTAT | 672 |
rs759922390 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064827 | TAGATTTGATTTGCA[-/T]TTTTTTTTTTTTTTT | 672 |
rs759950362 | snp | C/G | 1.68264e-05 | 0.0029005 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067733 | ATTATCATGAGTTAC[C/G]TCTAGCACACAGCTC | 672 |
rs760038328 | snp | A/G | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067646 | GTCTCTTCAGTAATT[A/G]GATTAGTTAAAGTGA | 672 |
rs760038355 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104466 | AACAAATACACAGAC[C/T]ATCAAAGTTATTTAG | 672 |
rs760098710 | in-del | -/CA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090906 | GAATGCAAAGGACAC[-/CA]CACACACGCATGTGC | 672 |
rs760109939 | snp | A/C/T | 4.95171e-05 | 0.00497559 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093689 | ATGCCTGGTAGAAGA[A/C/T]TTCCTCCTCAGCCTA | 672 |
rs760134035 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107506 | GTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 672 |
rs760138858 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054224 | CACATGGCGCTCCCC[C/T]GTGGTAAAGGCAGAA | 672 |
rs760169161 | in-del | -/CACACAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052810 | ACACACACACACACA[-/CACACAC]ACACACACTCTCTTA | 672 |
rs760188581 | in-del | -/G | 1.64966e-05 | 0.00287194 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049161 | TCCTTCACCACAGAA[-/G]CACCACACAGCTGTA | 672 |
rs760208409 | snp | A/G | 4.94271e-05 | 0.00497102 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057169 | AACCCATCAGGATAA[A/G]AGAAAGAGAAGCTTC | 672 |
rs760275914 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076473 | CCACAGCATCTTTAC[A/G]TTGATGTTTCTTACC | 672 |
rs760334657 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055855 | CAAGAATTGAACAAG[A/G]TTTGAACTTGGGAGG | 672 |
rs760396669 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047671 | GTCCTCTGTCCAGGC[A/G]TCTGGCTGCACAACC | 672 |
rs760464287 | snp | A/C | 5.5209e-05 | 0.00525371 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091071 | CAGATGTAAAAGCAG[A/C]CTATAAACGCTGCAA | 672 |
rs760465432 | in-del | -/CACACT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052819 | ACACACACACACACA[-/CACACT]CACACTCTCTTACTT | 672 |
rs760470280 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045063 | CCCACCTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 672 |
rs760491174 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099707 | TTATGACCAAGATTT[C/T]TGGCAAAACTATAAG | 672 |
rs760508069 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068618 | TAGCAGATATCATTC[A/G]ATTCCCTAAGATCGT | 672 |
rs760514235 | in-del | -/CT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046430 | TCAGATGGAGTCTCA[-/CT]CTGTCACTCAGGCTG | 672 |
rs760559327 | snp | A/G | 6.7077e-05 | 0.00579085 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063413 | GTTACATACAGCAGA[A/G]GAACGTGCTCTTTTC | 672 |
rs760579193 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097131 | AACTGCACATACATC[C/T]CTGAACCTAAAATAA | 672 |
rs760588785 | snp | A/G | 3.30753e-05 | 0.00406652 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092562 | TTACATTTAGTTTTA[A/G]CAAATGACTTGATGG | 672 |
rs760604247 | in-del | -/TA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100524 | TTGTGTGTGTGTGTG[-/TA]TATATATATATACAT | 672 |
rs760659424 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083732 | TTTTAAAATAATGAG[C/T]TCTTTTTGCTTATGG | 672 |
rs760662966 | in-del | -/AAGAAG | 0.000141585 | 0.00841265 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104084 | AGAAAAAAAAAAGAA[-/AAGAAG]AAGAAGAAGAAGAAG | 672 |
rs760676291 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067199 | ATAAAGTAATTGATT[C/G]ACTATTAGAAGACTA | 672 |
rs760677679 | snp | A/C | 1.79361e-05 | 0.00299462 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124155 | ATATATATCTTTTTA[A/C]AAGGTTTATAAAATG | 672 |
rs760760866 | in-del | -/A | 5.84402e-05 | 0.00540525 | intron-variant | BRCA1 | GRCh38.p7 | 17:43094908 | AACTGAATTGTCATT[-/A]AAAAAAATACATACT | 672 |
rs760770376 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072433 | TTTGAGAAGGGTCTC[A/G]GTCTGTCATCCAGGC | 672 |
rs760810832 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093289 | TTAACATGAGATCTT[C/T]GGGGTCTTCAGCATT | 672 |
rs760864137 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093174 | AGAGTGCTAACTTCC[A/G]GTAACGAGATACTTT | 672 |
rs760877199 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092761 | AGCCTGCAGTGATAT[C/T]AACTGTCTGTACAGG | 672 |
rs760899150 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099436 | CCACCACACCTGGCT[-/A]ATTTTTTATTTTTTG | 672 |
rs760922019 | snp | A/G | 1.64906e-05 | 0.00287142 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067630 | CATAACAACATGAGT[A/G]GTCTCTTCAGTAATT | 672 |
rs760923929 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103336 | GCCAGGTCTGGTGTC[G/T]TACCCCTGTAGTCCC | 672 |
rs760948037 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074982 | GAAAAGAAAAGGAAG[G/T]GAGGAAGGAAAGAAA | 672 |
rs760966872 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080344 | GGGATTACAGGCATG[A/T]GCCACCACGCCCGGC | 672 |
rs760989937 | snp | A/C | 1.65173e-05 | 0.00287374 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082390 | GATATCAGTGTTTGG[A/C]CAACAATACACACCT | 672 |
rs761045612 | in-del | -/AAAAAAAAAAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096379 | AGACTCTGTCTCAAA[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA | 672 |
rs761051875 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065089 | CCCGCCTTGGCCCCC[A/C]AAAGCGCTGGGATTA | 672 |
rs761108258 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067537 | GCGATTACAGGCATG[C/T]GCCACCGTGCCTCGC | 672 |
rs761143251 | in-del | -/A | 1.65048e-05 | 0.00287265 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091999 | CTGGACGCTTTTGCT[-/A]AAAAACAGCAGAACT | 672 |
rs761163190 | snp | A/G | 1.73006e-05 | 0.00294109 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063983 | ACTCAAAGGATTAGA[A/G]GTTGAAAACAAAATC | 672 |
rs761178502 | snp | C/T | 1.65553e-05 | 0.00287705 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093961 | GAGTCTTTTGAACTG[C/T]CAAATCTGCTTTCTT | 672 |
rs761211788 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089158 | TCTCTACTAAAAAAA[A/T]ACAAAAAAATGAGCT | 672 |
rs761271538 | snp | C/T | 1.81813e-05 | 0.00301502 | intron-variant, synonymous-codon | BRCA1 | GRCh38.p7 | 17:43079395 | TTGGCCATGTATATG[C/T]GAATCTGTAAGAAAG | 672 |
rs761274047 | in-del | -/TGTTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054441 | TGCTCAGTAGAAGGA[-/TGTTT]TGTTTTGTTTTGTTT | 672 |
rs761293595 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074446 | TTGAGATGGGTAGTT[C/T]CTATTCTGAAGACTC | 672 |
rs761329103 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103641 | GTCTCTCTCTTGATT[A/T]TATCAGGTACCCTGA | 672 |
rs761334121 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081971 | AGTGCAGTTCCTGAA[C/G]TATAGGATGTCTCTC | 672 |
rs761345513 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054128 | AAAAAATCCAAAGCA[C/T]TAGAATTTCTTTTTA | 672 |
rs761359856 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058378 | ACTCTGCTAAAAAAA[-/C]AACACACACACACAC | 672 |
rs761367765 | in-del | -/AA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062192 | TGAACTCCTGGGCTC[-/AA]AAGTGATTCTTCTGG | 672 |
rs761378771 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105901 | TTTGGGAGGCCGAGG[G/T]GGGCAGATCACCTGA | 672 |
rs761382531 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071343 | AAGTTAGGTTAAGAG[A/G]AAAATGGGTACATGA | 672 |
rs761414277 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43045810 | CCAATTGCTGGAGAC[-/A]AGAGAACACAAGCAG | 672 |
rs761424661 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091556 | GCTTTCAGACTGATG[C/T]CTCATTTGTTTGGAA | 672 |
rs761454371 | snp | A/C | 0.000232099 | 0.0107701 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110519 | TGAGCCTAGGAGGTC[A/C]AGGCAACAGTAAGCC | 672 |
rs761517096 | in-del | -/GAAG | 1.65883e-05 | 0.00287991 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104092 | AAAAGAAAAGAAGAA[-/GAAG]AAGAAGAAGAAAACA | 672 |
rs761585448 | snp | A/G | 1.656e-05 | 0.00287745 | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045686 | GCTGCAGTCAGTAGT[A/G]GCTGTGGGGGATCTG | 672 |
rs761604604 | in-del | -/CACACACT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052818 | ACACACACACACACA[-/CACACACT]CTCTTACTTTACCGC | 672 |
rs761617984 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106967 | TAGCATAAGAATAGA[C/T]ACATACATCAATAAA | 672 |
rs761640584 | snp | A/T | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082568 | TTATGTTGCATGGTA[A/T]CCCTCTGCTTCAAAA | 672 |
rs761664852 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059209 | TGGCTCACACCTGCA[A/C]TCCCAGCACTTTGGG | 672 |
rs761683937 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057161 | CCAAACACAACCCAT[C/T]AGGATAAGAGAAAGA | 672 |
rs761696956 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097023 | AGAAATTCAGAAAGA[A/G]AGCAAACAAAAAACT | 672 |
rs761700875 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112328 | CCTGACCTCGTGATC[C/T]GCCCACCTCAGCCTC | 672 |
rs761772015 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057026 | GTGGGGTGAGATTTT[C/T]GTCAACTTGAGGGAG | 672 |
rs761772657 | snp | G/T | 1.64868e-05 | 0.00287109 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047716 | ACCCTGGATCCCCAG[G/T]AAGGAAAGAGCATTC | 672 |
rs761886109 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103273 | GGAGTTCGAGACCAG[C/T]CTGACCAATATGGTG | 672 |
rs761913715 | snp | C/G | 1.64928e-05 | 0.00287161 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104837 | TCATGGACAGCACTT[C/G]AGTGTCATTCTTGGG | 672 |
rs761925468 | snp | C/G | 4.94287e-05 | 0.00497111 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43071138 | GGTTGAAGATGGTAT[C/G]TTGCCAACACGAGCT | 672 |
rs761976435 | in-del | -/CTATCTACCTAACTAT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109061 | TATCTACCTACCTAT[-/CTATCTACCTAACTAT]CTATCTGTCTACAGT | 672 |
rs761979956 | snp | C/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125801 | AAGGATTGTTGGGGG[C/G]GTGGAGGGAAATAAT | 672 |
rs762020342 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062427 | AGCTTTTCTTCAACA[A/T]CAGTGAACAGTTTTC | 672 |
rs762028824 | snp | A/G | 2.05645e-05 | 0.00320653 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091023 | CTCTCACACCCAGAT[A/G]CTGCTTCACCTTAAA | 672 |
rs762068981 | snp | A/C/T | 3.6596e-05 | 0.00427749 | intron-variant, missense | BRCA1 | GRCh38.p7 | 17:43079354 | ATATGTTCTCTAGGC[A/C/T]TTTTAGAAAACATGG | 672 |
rs762074644 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073512 | TGTCTTTTATGATAA[C/T]GTGTTTTTGAGGATT | 672 |
rs762104993 | in-del | ACTTTGGGAGAGGT/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108768 | GCCTGTAATCCCAAC[ACTTTGGGAGAGGT/C]CAGGAGTTCAAGACC | 672 |
rs762106694 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058295 | TGGAGGATCACTTGA[G/T]CCCAGGAGTTGGAGG | 672 |
rs762136074 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117276 | GTGAAACCCTGTCTA[C/T]GCTAAAAATACAAAA | 672 |
rs762153716 | snp | C/G | 2.58943e-05 | 0.00359812 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43090930 | GCATGTGCACACACA[C/G]ACACGCTTTTTACCT | 672 |
rs762224894 | snp | A/C | 3.29533e-05 | 0.00405901 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099767 | CTTAAAAAACCTGAG[A/C]CCCTTACCCAATTCA | 672 |
rs762224984 | in-del | -/CT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077363 | TGAGACGGAGTCTCA[-/CT]CTGTTGCCCAAGCTG | 672 |
rs762240769 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046928 | CTGTAATTTAACGAT[A/G]TGGAAAAATGTATGT | 672 |
rs762287920 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047872 | TGCCTCCTGGGCTCA[A/G]GCAATCCTTCCATCT | 672 |
rs762310583 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092875 | ACCCAGAGTGGGCAG[A/G]GAATGTTGCACATTC | 672 |
rs762363239 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118089 | GTGAGATGTACATGG[A/G]GGGAGTCAGGAAAGG | 672 |
rs762365238 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101540 | CAGAGTCTCACTCTA[C/T]GGCCCAGGCTGGAGT | 672 |
rs762421226 | in-del | -/ATC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073343 | AATAAATCAGCAGAT[-/ATC]ATTACCAAATTAAAA | 672 |
rs762444270 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063506 | TTCCCTCTAAAGCCA[C/T]AGCCCTTTAATAAGG | 672 |
rs762477679 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095717 | TTGACAGAGAATGAT[A/G]CTCTAACTCTGCCAA | 672 |
rs762493731 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073764 | TATATATATATATAT[-/A]TATTTTTTGAGATGG | 672 |
rs762519154 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118293 | GGAGGATATTGTAGG[C/G]AAAGACTATCAGAGA | 672 |
rs762526216 | snp | C/T | 1.75508e-05 | 0.00296228 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106449 | GCATCATTACCAAAT[C/T]ATATACCTTTTGGTT | 672 |
rs762552027 | snp | G/T | 3.32281e-05 | 0.0040759 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045665 | GTGGCTCTGTACCTG[G/T]GGCTGGCTGCAGTCA | 672 |
rs762589415 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092737 | TATCTTTCTGACCAA[C/T]CACAGGAAAGCCTGC | 672 |
rs762635795 | in-del | -/C | 1.64762e-05 | 0.00287016 | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104217 | CATCTTTTAGATGTT[-/C]AGGAGAGTTATTTTC | 672 |
rs762639544 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120237 | TGTCAGAAATAGCTG[C/T]CAATATTGACTTAGA | 672 |
rs762641426 | snp | A/C | 1.65146e-05 | 0.0028735 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045574 | ATTTAGTAGCCAGGA[A/C]AGTAGAAGGACTGAA | 672 |
rs762642319 | snp | C/T | 1.65564e-05 | 0.00287714 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093953 | CATTTCAGGAGTCTT[C/T]TGAACTGCCAAATCT | 672 |
rs762663053 | in-del | -/A | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127478 | GTTTGCAAATGCACC[-/A]ATCAGCACTCTGTGT | 672 |
rs762671930 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051334 | AGATCTTCTTGAAGT[A/G]CATATGTAGTTGACC | 672 |
rs762709502 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110501 | TGAGGTGATAGGATC[A/G]CTTGAGCCTAGGAGG | 672 |
rs762729313 | snp | A/G | 1.69046e-05 | 0.00290723 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063958 | ACTCAGCATCTGCAG[A/G]ATGAAAAACACTCAA | 672 |
rs762744684 | snp | A/T | 1.65045e-05 | 0.00287263 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092130 | CTTCCCATAGGCTGT[A/T]CTAAGTTATCTGAAA | 672 |
rs762772420 | snp | C/G | 3.29641e-05 | 0.00405968 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093551 | GTTTCTGCTGTGCCT[C/G]ACTGGCATTTGGTTG | 672 |
rs762779289 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057013 | GGAATACAGAGTGGT[A/G]GGGTGAGATTTTTGT | 672 |
rs762816348 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127022 | GCCCGCCTGCACCCC[A/G]CTTGAATTCTCACCG | 672 |
rs762827028 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088533 | AATGTCTTCAAGGTT[C/T]GTCCATGGATGATTT | 672 |
rs762858345 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112034 | GTTATTCAGATTATA[C/T]TGATATTACAGAAGA | 672 |
rs762867923 | snp | C/T | 1.66236e-05 | 0.00288297 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094781 | CTCAGCTGCACGCTT[C/T]TCAGTGGTGTTCAAA | 672 |
rs762883588 | snp | C/T | 0.000132842 | 0.00814882 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074299 | AGAGTAAAATCAAAG[C/T]GTTTGTTCCAATACA | 672 |
rs762908108 | snp | C/T | 3.29554e-05 | 0.00405914 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091510 | CTTCATCATCTGAAA[C/T]CAATTCCTTGTCACT | 672 |
rs762925849 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101430 | TTGAACTCTAGGACT[C/T]GAGATCCACCCGCCT | 672 |
rs762948688 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107383 | TTTTTATTTTCTTAA[-/T]TTTTTTTTTTTTTTT | 672 |
rs762956862 | snp | A/C | 3.30055e-05 | 0.00406222 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43094697 | TAATGAGCTGGCATG[A/C]GTATTTGTGCCACAT | 672 |
rs762999974 | snp | C/G | 1.64885e-05 | 0.00287123 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070892 | AGAATGTTGTTAAGT[C/G]TTAGTCATTAGGGAG | 672 |
rs763051683 | snp | C/T | 1.64985e-05 | 0.0028721 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094261 | TTTTCTCTGAAGAAC[C/T]AGAATATTCATCTAC | 672 |
rs763074389 | snp | C/G/T | 0.000195844 | 0.00989383 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090920 | CCACACACACGCATG[C/G/T]GCACACACACACACG | 672 |
rs763088865 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100135 | AGTTCAAGACCAGCA[G/T]AAGCAACAGAGTGAG | 672 |
rs763110421 | in-del | -/ACTTCATTAGTACTGGAACCT | 1.64787e-05 | 0.00287038 | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092370 | TTAATACTGGAGCCC[-/ACTTCATTAGTACTGGAACCT]ACTTCATTAATATTG | 672 |
rs763155937 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099929 | GTTGGCCAGTTCTGT[A/G]CTTTTCCTCCTGAAG | 672 |
rs763169190 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075268 | CATTCTTTCTACTCA[A/G]TTTTAGCAGAATTCA | 672 |
rs763180418 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049257 | TAACCCAGGCCCTCT[A/C]CCCTACACTCTCCGG | 672 |
rs763215241 | in-del | -/TTAAAAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112457 | ATCTCTACAAGAAAC[-/TTAAAAA]TTAGCTGGGCAAATG | 672 |
rs763230080 | snp | C/T | 6.6107e-05 | 0.00574884 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124061 | AGCATTAATGACATT[C/T]TGTACTTCTTCAACG | 672 |
rs763351631 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094398 | TTAACTTTCTGAATG[C/T]TGCTATTTAGTGTTA | 672 |
rs763354142 | snp | C/G/T | 1.64768e-05 | 0.00287021 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43091831 | AAGGTATATTGTTTA[C/G/T]TTTACCAAATAACAA | 672 |
rs763381062 | snp | A/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104239 | GTTATTTTCCTTTTT[A/T]GCAAAATTATAGCTG | 672 |
rs763395672 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115834 | CTCAATAATTTATTT[A/G]AAAATAAAGCTATTC | 672 |
rs763484977 | snp | A/G | 3.29565e-05 | 0.00405921 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045806 | TCTGCCCAATTGCTG[A/G]AGACAGAGAACACAA | 672 |
rs763492078 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062169 | TATGATCATAGCTCA[C/T]TGCAGCCTTGAACTC | 672 |
rs763535861 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096995 | TACTTGAGGGAGGAA[A/G]GTGGGAAGAGGGAGA | 672 |
rs763538386 | snp | C/T | 1.65869e-05 | 0.00287979 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074303 | TAAAATCAAAGTGTT[C/T]GTTCCAATACAGCAG | 672 |
rs763596987 | snp | A/G | 1.64874e-05 | 0.00287113 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091449 | CCTAAGTTTGAATCC[A/G]TGCTTTGCTCTTCTT | 672 |
rs763602037 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051365 | TGCACTCTACAGGCA[C/T]TCTTTGTCATTCAAG | 672 |
rs763633355 | snp | A/G | 0.000424744 | 0.0145668 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106556 | TTATAAAGAAAGAAA[A/G]AACAATTTAATTTAC | 672 |
rs763639161 | snp | A/C | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092740 | CTTTCTGACCAACCA[A/C]AGGAAAGCCTGCAGT | 672 |
rs763650426 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080978 | ATTTAGGGAGAAAAA[A/G]GCTCAAAACTTATGT | 672 |
rs763740623 | snp | A/T | 1.65564e-05 | 0.00287714 | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045683 | CTGGCTGCAGTCAGT[A/T]GTGGCTGTGGGGGAT | 672 |
rs763761005 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118334 | AACTTCTGGTAGGAA[C/T]CTATAGGCTATTTTA | 672 |
rs763794005 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105646 | TTGAAAACACATAGA[A/T]AACAATGTCCAAAGG | 672 |
rs763829102 | snp | G/T | 5.17023e-05 | 0.00508414 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045579 | GTAGCCAGGACAGTA[G/T]AAGGACTGAAGAGTG | 672 |
rs763845063 | snp | A/G | 1.65061e-05 | 0.00287277 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092611 | GATATGGGTTTTGTA[A/G]AAGTCCATGTTTATT | 672 |
rs763847918 | snp | G/T | 0.000380344 | 0.013785 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057017 | TACAGAGTGGTGGGG[G/T]GAGATTTTTGTCAAC | 672 |
rs763879281 | in-del | -/AG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090060 | AAGGGAAAAAAAAAA[-/AG]AAGAAGAGAAAGAAG | 672 |
rs763888109 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068138 | AAAAATTAGCCAGGC[G/T]TGGTGGCGGGCACCT | 672 |
rs763949697 | in-del | -/TT | 2.09637e-05 | 0.0032375 | intron-variant | BRCA1 | GRCh38.p7 | 17:43095808 | TATCTACCCACTCTC[-/TT]TTCAGTGCCTGTTAA | 672 |
rs764009120 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093554 | TCTGCTGTGCCTGAC[C/T]GGCATTTGGTTGTAC | 672 |
rs764013144 | snp | A/G | 3.30098e-05 | 0.00406249 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092135 | CATAGGCTGTTCTAA[A/G]TTATCTGAAATCAGA | 672 |
rs764015648 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071034 | ACACTTTCTTCCATT[A/G]CATTATACCCAGCAG | 672 |
rs764015959 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123019 | CTGAGATCGCGCCAC[C/T]GCACTCCAGCCTGGG | 672 |
rs764016240 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074418 | CCACATCAACAACCT[C/T]AATGAGCTCCTCTTG | 672 |
rs764069403 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125686 | GCTGTACGAAGGTCA[C/G]AATCGCTACCTATTG | 672 |
rs764142982 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085314 | GCAGTGAGCTGAGAT[C/T]GTGCCACGGCACTCC | 672 |
rs764167847 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047487 | TACAATATAAAACAA[A/G]TAACAATAAAAACAT | 672 |
rs764186025 | snp | A/G | 1.64977e-05 | 0.00287203 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094267 | CTGAAGAACCAGAAT[A/G]TTCATCTACCTCATT | 672 |
rs764211700 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087148 | AATTTAGTAACATGT[A/G]TCAAACACCAAAATC | 672 |
rs764231119 | snp | A/C | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104177 | GCACGGTTTCTGTAG[A/C]CCATACTTTGGATGA | 672 |
rs764247675 | in-del | -/TA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100525 | TTGTGTGTGTGTGTG[-/TA]TATATATATACATAT | 672 |
rs764256814 | snp | C/T | 1.64885e-05 | 0.00287123 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070893 | GAATGTTGTTAAGTC[C/T]TAGTCATTAGGGAGA | 672 |
rs764267364 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105619 | TTTCTGTCAAATTAT[C/G]ATTATACTTCTTTGA | 672 |
rs764299669 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101462 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCAAG | 672 |
rs764332909 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077271 | ACATGGAACTAATGA[C/T]GAAATGGCACAAGAA | 672 |
rs764371150 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108707 | GGAAGACTCTGTCTC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAGG | 672 |
rs764443206 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111576 | CTTGTAATCCCAGAA[C/T]TTAGGGAGGCCAAGG | 672 |
rs764447564 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100163 | GAGACCCAGTCTCTA[A/C]AAAATAATAGTAGTA | 672 |
rs764458412 | snp | A/C | 3.29707e-05 | 0.00406008 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092255 | ACTTTGTTTATAGAC[A/C]TCAGGTTGCAAAACC | 672 |
rs764485811 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060859 | GGCCGGGCACAGTGG[C/T]TCACACCTGTGATCC | 672 |
rs764499766 | snp | C/G | 5.22052e-05 | 0.00510881 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095893 | CTGGTTCCTTGAGGG[C/G]TGATTTGTAACAATT | 672 |
rs764503776 | snp | C/G/T | 3.29991e-05 | 0.00406185 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076645 | GAAAACAAATCTACT[C/G/T]TACTGCTTTGTTCTG | 672 |
rs764505044 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114240 | ACTGGGCCCTTGAGT[A/C]CCTGTAATAATAGTA | 672 |
rs764567792 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076424 | GTGAAAAAAATTAAC[A/G]ATCAGAGTTCAATAT | 672 |
rs764575760 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075396 | AAATAGTTCCTCTGC[G/T]CTTCCAAGTGCTTAG | 672 |
rs764625123 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079189 | CAAACAAAAACAAAA[C/G]AAAACAAAACAAAAA | 672 |
rs764641904 | snp | C/T | | | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044260 | AGGCTCTGAGAAAGT[C/T]GGCTGGCCTAAGTCT | 672 |
rs764701960 | in-del | -/AAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104086 | AAAAAAAAAGAAAAG[-/AAG]AAGAAGAAGAAGAAG | 672 |
rs764704412 | snp | C/G | 0.000185822 | 0.00963724 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045161 | CTCCCCAATGTTCCA[C/G]TCCAACATTTGAGAA | 672 |
rs764707052 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055157 | CTCAGGCCTGACAGG[-/T]TAAGTGTGAAATCTT | 672 |
rs764800682 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117439 | ACAGAGGAAGACTCT[A/G]TCTCAAAAAAAAGAA | 672 |
rs764874551 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071384 | GGTGGAAATCCAAAG[C/T]AGCTTAGTTTCCTAA | 672 |
rs764884677 | in-del | -/AA | 0.000115665 | 0.00760389 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104102 | AAGAAGAAGAAGAAG[-/AA]GAAAACAAATGGTTT | 672 |
rs764891781 | snp | C/T | 8.314e-05 | 0.00644695 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43063932 | ATATTTCAGTGTCCG[C/T]TCACACACAAACTCA | 672 |
rs764936673 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064028 | TAAGAAGCTAAAGAG[C/G]CTCAGTTTTTTACAC | 672 |
rs764977822 | snp | G/T | 1.75631e-05 | 0.00296332 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063829 | GTGTAAAAATGCAAT[G/T]CTGAGGTGTTAAAGG | 672 |
rs764997373 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068860 | GGGGTTCATGTTCTT[C/T]CCCAAAGAAATTTAG | 672 |
rs765040547 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123324 | CTTCCAAATACCTAT[-/C]CTCTCAACGACACCG | 672 |
rs765094584 | in-del | -/TTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048060 | CCCAGCCTTGGCTAA[-/TTT]TTAATAATTTTTTTG | 672 |
rs765156052 | snp | G/T | 1.6495e-05 | 0.0028718 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091440 | GTTCCAATACCTAAG[G/T]TTGAATCCATGCTTT | 672 |
rs765157365 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093027 | CTGTGGTTAACTTCA[C/T]GTCCCAATGGATACT | 672 |
rs765171317 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056094 | GCATAATTACAGTAC[A/G]TAGCTCATAGAGTTG | 672 |
rs765183110 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082527 | CAGCTTCTAGTTCAG[C/T]CATTTCCTGCTGGAG | 672 |
rs765189603 | snp | G/T | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071157 | CCAACACGAGCTGAC[G/T]CTGGGGCTCTGTCTT | 672 |
rs765209391 | snp | A/G | 6.41334e-05 | 0.00566238 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091302 | AGCACCTTAGGAGGA[A/G]CATGTTTCAAGTTTA | 672 |
rs765241963 | snp | A/T | 3.29707e-05 | 0.00406008 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067651 | TTCAGTAATTAGATT[A/T]GTTAAAGTGATGTGG | 672 |
rs765266479 | in-del | -/AAG | 0.00017014 | 0.00922178 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091317 | ACATGTTTCAAGTTT[-/AAG]AAGCAGTTCCTTTAA | 672 |
rs765295071 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045421 | TTGGTGGCGTTTAAA[C/T]GGTTTTAAAATCTTC | 672 |
rs765323349 | snp | A/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094479 | TGCTTATTCCATTCT[A/T]TTCTCTCACACAGGG | 672 |
rs765422008 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122706 | TTGAGGTCAGGAGTT[G/T]GAGACCAGCATGGCC | 672 |
rs765432756 | snp | C/T | 1.6473e-05 | 0.00286988 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43099800 | GTAGACAGACGTCTT[C/T]TGAGGTTGTATCCGC | 672 |
rs765476375 | in-del | -/AAAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057840 | ACTCCGTCTCAAAAC[-/AAAC]AAACAAACAAACAAA | 672 |
rs765485378 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084752 | TCTGCAGCAATGCCA[C/T]TGCCACCACGTGGTA | 672 |
rs765489669 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047370 | CCTCCCAAAGTGCTG[A/G]AATTATAGGCATGAG | 672 |
rs765623980 | snp | A/C | 0.000365163 | 0.0135073 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110581 | CAACAGAGTAAGACC[A/C]TGTCTCAAAAAAAAA | 672 |
rs765632953 | in-del | -/ATATAAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100568 | TGTGTGTATATATAT[-/ATATAAC]ATATATATAACATAT | 672 |
rs765634136 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052692 | GCTTCAAAGAGACTG[C/T]GATAGAGAAAAAAAT | 672 |
rs765656957 | snp | G/T | 0.000115849 | 0.00760993 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43045698 | AGTGGCTGTGGGGGA[G/T]CTGGGGTATCAGGTA | 672 |
rs765681061 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045802 | CACATCTGCCCAATT[A/G]CTGGAGACAGAGAAC | 672 |
rs765687131 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127166 | CCCCCTGCTCCTCAG[C/T]GCCCGGTCCCATCGA | 672 |
rs765695342 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090533 | GCATTGGCCACCACG[C/T]CCAGCTAATTTTTGT | 672 |
rs765728864 | snp | A/G | 6.76601e-05 | 0.00581597 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067738 | CATGAGTTACCTCTA[A/G]CACACAGCTCAGAAT | 672 |
rs765729710 | snp | C/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091593 | ATCAAGAAAGGATCC[C/T]GGGTGTTTGTATTTG | 672 |
rs765804641 | snp | G/T | 0.000181934 | 0.00953593 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044352 | CAACATTTACAAAAC[G/T]TATTTTGTACAATCA | 672 |
rs765826347 | snp | C/G | 1.64762e-05 | 0.00287016 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057171 | CCCATCAGGATAAGA[C/G]AAAGAGAAGCTTCCT | 672 |
rs765845161 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109022 | AACAAAACAAAAAAA[A/C]CCCAACTATATCTAT | 672 |
rs765846390 | snp | C/T | 1.68069e-05 | 0.00289882 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063417 | CATACAGCAGAAGAA[C/T]GTGCTCTTTTCACGG | 672 |
rs765880690 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054323 | CAGGCTGACCTCAGC[A/C]GTTCAAAACTCCAGG | 672 |
rs765950064 | snp | A/G | 1.74318e-05 | 0.00295222 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43095864 | TTTTTGCAGAATCCA[A/G]ACTGATTTCATCCCT | 672 |
rs765966166 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075510 | TGGGTCAAATACTAA[A/G]GCTAGGCCCCCTGGA | 672 |
rs765993367 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116165 | AAAATTTTCTGCTTA[G/T]ATTTCTTTTGAATTC | 672 |
rs766004110 | snp | C/T | 1.65384e-05 | 0.00287557 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124028 | TTACCAGATGGGACA[C/T]TCTAAGATTTTCTGC | 672 |
rs766089932 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077487 | AGGTGCCTGCCACCA[C/T]GCCCAGCTAGTTTTT | 672 |
rs766092076 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045084 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 672 |
rs766094343 | snp | C/T | 6.10258e-05 | 0.00552351 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091079 | AAAGCAGACTATAAA[C/T]GCTGCAACTTGCTGT | 672 |
rs766167206 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43061361 | CTGTATATTTCTCCA[C/T]AGCATTTATTGTTAT | 672 |
rs766169604 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084448 | TGGGATTACAGACGT[G/T]AGTCACTGTGCCTGG | 672 |
rs766172481 | snp | C/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127251 | ACTAGGTGAAGCCAG[C/G]TGGGCTCCTGAGTCA | 672 |
rs766220679 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120668 | TACTTGGGGGGCCGA[C/G]GCAGGAGAATGGCGT | 672 |
rs766257325 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43053248 | CATGCTCATAATGCT[A/G]GAAGTTCTCCCCAGG | 672 |
rs766289632 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107725 | CAAACAGTGTTGAGA[A/C]AAAAGTATAACCACA | 672 |
rs766291723 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068641 | AAGATCGTTTCTTTG[C/T]ATAGTGACACTCTAC | 672 |
rs766305255 | snp | A/G | 4.94173e-05 | 0.00497053 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071073 | GTATGAGCAGCAGCT[A/G]GACTCTGGGCAGATT | 672 |
rs766330646 | snp | C/T | 2.44197e-05 | 0.00349418 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090939 | CACACACACACGCTT[C/T]TTACCTGAGTGGTTA | 672 |
rs766347954 | snp | A/G | 0.000193555 | 0.00983564 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125348 | CACAGCCTGTCCCCC[A/G]TCCAGGAAGTCTCAG | 672 |
rs766373028 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068277 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGA | 672 |
rs766381694 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092425 | AGCTGGCTTCTTTAA[A/G]AACATTTTCTCTAAT | 672 |
rs766447664 | snp | A/G | 1.65833e-05 | 0.00287948 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091955 | ATGTGTATGGGTGAA[A/G]GGGCTAGGACTCCTG | 672 |
rs766477679 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059578 | CTTTCCCACTCCCCC[A/G]TATTCCCTACCATGC | 672 |
rs766484283 | snp | C/G | 1.65241e-05 | 0.00287433 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104251 | TTTTGCAAAATTATA[C/G]CTGTTTGCATCTGTA | 672 |
rs766539298 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101507 | GCTAGAACAATTACT[C/T]TTTTTTCTTTTTTGA | 672 |
rs766572561 | snp | A/C/T | 0.00013186 | 0.00811874 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091872 | CAGGGAAGCTCTTCA[A/C/T]CCTCACTAGATAAGT | 672 |
rs766586132 | snp | A/G | 1.79338e-05 | 0.00299443 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124156 | TATATATCTTTTTAA[A/G]AGGTTTATAAAATGA | 672 |
rs766614917 | snp | C/T | 1.65723e-05 | 0.00287852 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051060 | GTTCTCCCAGGCTCT[C/T]ACCTGTGGGCATGTT | 672 |
rs766631311 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112956 | TTACAGGCATGCGCC[C/T]CCACGCCCGTCTAAT | 672 |
rs766673300 | snp | G/T | 3.49815e-05 | 0.00418205 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045594 | GAAGGACTGAAGAGT[G/T]AGAGGAGCTCCCAGG | 672 |
rs766678487 | in-del | -/AAAAAAAAAAAAAAAAGAAAAGAAAACACAAACAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106119 | CAGGACCCTGTCTTA[lengthTooLong]AAAAAAAAAAAAAAA | 672 |
rs766700840 | snp | C/T | 1.65181e-05 | 0.00287381 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049187 | CTGTACCATCCATTC[C/T]AGTTGATCTAAAATG | 672 |
rs766761270 | snp | A/G | 1.73177e-05 | 0.00294254 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063984 | CTCAAAGGATTAGAA[A/G]TTGAAAACAAAATCA | 672 |
rs766784305 | snp | A/G | 1.64863e-05 | 0.00287104 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43067640 | TGAGTAGTCTCTTCA[A/G]TAATTAGATTAGTTA | 672 |
rs766804544 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103409 | GAGGCGGAGGTTGCA[A/G]TGAGCTGACATCGTG | 672 |
rs766836245 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090285 | GAGCTATGCAGAGTC[C/T]CTTGAATCATCCTGC | 672 |
rs766861977 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088305 | CATCAAACAGTAACT[-/C]CCCATTTCCCCCTCC | 672 |
rs766863114 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065283 | GTGGTATAATTTTCA[C/T]GAGTAAGTGGAAACC | 672 |
rs766885850 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050767 | ACCTATCCAAAGATA[C/T]TTTCTCACTAACATG | 672 |
rs766934857 | snp | C/T | 1.6554e-05 | 0.00287693 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093962 | AGTCTTTTGAACTGC[C/T]AAATCTGCTTTCTTG | 672 |
rs766938984 | in-del | -/CTCT | 6.7706e-05 | 0.00581794 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049094 | AATATTGTGTCCTCC[-/CTCT]CTGACAGGGCACCCA | 672 |
rs766950602 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057032 | TGAGATTTTTGTCAA[C/T]TTGAGGGAGGGAGCT | 672 |
rs766962460 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074450 | GATGGGTAGTTTCTA[C/T]TCTGAAGACTCCCAG | 672 |
rs767008621 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075637 | CACGGTCCCAGCTCA[-/C]CTGCAACCTCTGCCT | 672 |
rs767008841 | snp | A/G | 1.64887e-05 | 0.00287125 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076453 | ATAAATAAAGATGTC[A/G]GATACCACAGCATCT | 672 |
rs767064138 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051576 | CTCAAGTACTCACTA[G/T]GACCCCATCAACAGA | 672 |
rs767144634 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115790 | CCAGACTAGCAGGGT[A/G]GGGGGGGAGAAAAAG | 672 |
rs767217821 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092406 | ACTTCATTAATATTG[C/T]TTGAGCTGGCTTCTT | 672 |
rs767224147 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059241 | GGCCGAGGTGGGTGG[A/T]TTACCTGAGGTCAGG | 672 |
rs767246037 | snp | G/T | 1.6483e-05 | 0.00287076 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091470 | TGCTCTTCTTGATTA[G/T]TTTCTTCCAAGCCCG | 672 |
rs767347357 | snp | A/T | 0.000297959 | 0.0122021 | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43044257 | AAAAGGCTCTGAGAA[A/T]GTCGGCTGGCCTAAG | 672 |
rs767388616 | in-del | -/TTT | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044805 | CTAGTTTCATTTTCC[-/TTT]TTTTTTTTTTTTTTT | 672 |
rs767421571 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082571 | TGTTGCATGGTATCC[C/T]TCTGCTTCAAAAACG | 672 |
rs767435205 | snp | A/G | 3.29495e-05 | 0.00405877 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057165 | ACACAACCCATCAGG[A/G]TAAGAGAAAGAGAAG | 672 |
rs767450523 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082052 | TTATAAGGAATATGT[C/T]TGAGTACTTTTTCAT | 672 |
rs767459025 | snp | C/T | 0.000115509 | 0.00759875 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049175 | AGCACCACACAGCTG[C/T]ACCATCCATTCCAGT | 672 |
rs767468738 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120569 | AGGAAGTGGAGACCA[G/T]CCTGGCTAACACGGT | 672 |
rs767471562 | in-del | -/AAAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090050 | TAGATTTTAAAAGGG[-/AAAA]AAAAAAAGAAGAAGA | 672 |
rs767530204 | snp | C/T | 1.64836e-05 | 0.0028708 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093572 | CATTTGGTTGTACTT[C/T]TTTTTCTTTATCTCT | 672 |
rs767544239 | snp | A/C | 1.64822e-05 | 0.00287068 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092264 | ATAGACCTCAGGTTG[A/C]AAAACCCCTAATCTA | 672 |
rs767571709 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083384 | TGGTCTTGAACTCCT[A/G]ACCTCAAGTGATCAG | 672 |
rs767583964 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073243 | TAGCAATTTTGTAAG[-/A]AAGGAAAAAAAAGTT | 672 |
rs767595162 | in-del | -/AC | 1.65051e-05 | 0.00287267 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093687 | TATGCCTGGTAGAAG[-/AC]ACTTCCTCCTCAGCC | 672 |
rs767604013 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072115 | AGTACAGGCCGGGTG[C/T]GGTGGCTCAGGCCTG | 672 |
rs767641736 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089036 | AAAATTAGGAGGCCA[A/G]GCCTGGTGGCTCACG | 672 |
rs767661294 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080662 | ATAAAAAAAAAAATT[A/T]GCTGGGTATGGTGGT | 672 |
rs767666029 | snp | A/T | 3.29598e-05 | 0.00405941 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093035 | AACTTCATGTCCCAA[A/T]GGATACTTAAAGCCT | 672 |
rs767666190 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094456 | GATTCTCTGAGCATG[A/G]CAGTTTCTGCTTATT | 672 |
rs767720128 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094792 | GCTTCTCAGTGGTGT[C/T]CAAATCATTATTACT | 672 |
rs767787535 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111215 | TATCTTTTTTTATAG[G/T]CTTCATAAAAGATTT | 672 |
rs767849754 | snp | A/C | 3.29799e-05 | 0.00406065 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104844 | CAGCACTTGAGTGTC[A/C]TTCTTGGGATATTCA | 672 |
rs767857463 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126606 | ATGAGAGAGCCCTTC[A/G]TGTTCTGAGGGACCG | 672 |
rs767903443 | snp | C/T | 1.6507e-05 | 0.00287284 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076656 | TACTTTACTGCTTTG[C/T]TCTGATAGTGATAAT | 672 |
rs767911101 | in-del | -/CAAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115036 | TGATTACAAAGCGGG[-/CAAA]CACTGACCCTTAGAA | 672 |
rs767929702 | in-del | AGAAAAAAAAAAGAAAAG/GAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104069 | TCTCAAAAAAAAAAA[AGAAAAAAAAAAGAAAAG/GAA]AAGAAGAAGAAGAAG | 672 |
rs767958299 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091846 | CTTTACCAAATAACA[A/G]GTGTTGGAAGCAGGG | 672 |
rs767990219 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063627 | TTAAATAAATCCCTA[C/G]CTCATATGCTAACAT | 672 |
rs767992810 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117285 | TGTCTACGCTAAAAA[C/T]ACAAAAATTAGCCGG | 672 |
rs768001441 | snp | A/G/T | 3.29717e-05 | 0.00406015 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43092967 | GTATTCTGCAAATAC[A/G/T]GAGCATCAAGTTCAC | 672 |
rs768054411 | snp | C/G | 1.64841e-05 | 0.00287085 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094174 | CTTCAATATTACTCT[C/G]TACTGATTTGGAGTG | 672 |
rs768065380 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108361 | AAAAGGCATTGGGAA[A/T]TGTGAGAAAAGACAC | 672 |
rs768065826 | snp | C/T | 8.26139e-05 | 0.00642652 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43097273 | CTTATTAACGGTATC[C/T]TCAGAAGAATCAGAT | 672 |
rs768092833 | in-del | -/CACACACACGCATGTGCA | 3.72488e-05 | 0.00431544 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090906 | GAATGCAAAGGACAC[-/CACACACACGCATGTGCA]CACACACACACGCTT | 672 |
rs768122636 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081931 | CTAACAGGAGCTCTA[C/T]ATCACTAGGCTTTCT | 672 |
rs768122642 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099395 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 672 |
rs768200575 | snp | C/T | 3.21507e-05 | 0.00400928 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124141 | TTAGAAAAACATATA[C/T]ATATATCTTTTTAAA | 672 |
rs768212175 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096896 | AAAAAGGGTATTTCC[G/T]CCACTATAAAATGAG | 672 |
rs768239314 | snp | G/T | 1.64773e-05 | 0.00287026 | missense, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045779 | CTCGGGTCACCACAG[G/T]TGCCTCACACATCTG | 672 |
rs768261282 | in-del | -/CACT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052821 | ACACACACACACACA[-/CACT]CACTCTCTTACTTTA | 672 |
rs768302379 | in-del | -/AA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058019 | GTGAAACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 672 |
rs768327850 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082488 | GGTAGCTGTTAGAAG[A/G]CTGGCTCCCATGCTG | 672 |
rs768401297 | in-del | -/C | 1.6477e-05 | 0.00287024 | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045784 | TCACCACAGGTGCCT[-/C]CACACATCTGCCCAA | 672 |
rs768416164 | snp | C/G | 1.67413e-05 | 0.00289316 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094793 | CTTCTCAGTGGTGTT[C/G]AAATCATTATTACTG | 672 |
rs768440647 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113657 | TAGGCGTGAGCCACC[A/G]CGCCCGTCCTCTATT | 672 |
rs768462633 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057152 | TGAAAGAAACCAAAC[A/G]CAACCCATCAGGATA | 672 |
rs768492260 | snp | C/T | 3.61808e-05 | 0.00425312 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074555 | GGAGAAAACCATCGC[C/T]ACCAATTGTGAAAGG | 672 |
rs768510015 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089919 | AGCTGAGGTAGGAGG[A/G]TCGCTTGAGCCCAGG | 672 |
rs768566997 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126294 | GGGTGGTCGTTTTGA[A/G]GGACAAGTGGTAAGA | 672 |
rs768583394 | snp | C/T | 1.66818e-05 | 0.00288802 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123979 | CATAGGAGATAATCA[C/T]AGGAATCCCAAATTA | 672 |
rs768647585 | in-del | -/A | 3.74483e-05 | 0.00432698 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115706 | TAATAATGGAGCCAC[-/A]ATAACACATTCAAAC | 672 |
rs768688043 | snp | C/T | 0.000237614 | 0.0108973 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044880 | ATGATCTTGGCTCAC[C/T]GCAACCTCCACCTCC | 672 |
rs768709829 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119022 | CCATCTGCCTCGACC[A/G]GGATTACAGGCGTGA | 672 |
rs768720716 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088738 | AGGATGAATCGAGGG[G/T]GTCTGAACAGCTTCA | 672 |
rs768730453 | snp | C/T | 6.05455e-05 | 0.00550174 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045424 | GTGGCGTTTAAATGG[C/T]TTTAAAATCTTCTCA | 672 |
rs768735867 | in-del | -/G | 0.000552859 | 0.016617 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104086 | AAAAAAAAAAGAAAA[-/G]AAGAAGAAGAAGAAG | 672 |
rs768740518 | snp | A/G | 1.64963e-05 | 0.00287192 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104831 | GAGTTTTCATGGACA[A/G]CACTTGAGTGTCATT | 672 |
rs768765042 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117977 | TCTAGTGTGGTAGAC[A/G]GTTGATACGGAATTA | 672 |
rs768766245 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058989 | AAGGCAAGAGTATAA[C/G]CACTGGCTATTACTA | 672 |
rs768838029 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045158 | TTCCTCCCCAATGTT[C/T]CACTCCAACATTTGA | 672 |
rs768857035 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105042 | AAAGACATGTAAACA[A/G]ATAAAAATAAGATGC | 672 |
rs768862176 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43080192 | ATGGGCCACACCAAA[C/T]ATTTAATAAACTTAC | 672 |
rs768904580 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093241 | TACTGCTACTCTCTA[C/T]AGATCTTTCAGTTTG | 672 |
rs768924063 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095374 | ACTGCTTGAGTCCAG[A/G]AGTTTGAGACCAGCC | 672 |
rs768945711 | snp | C/G | 1.65496e-05 | 0.00287655 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071201 | TTCAGGGTCATCAGA[C/G]AAGAGGCTGATTCCA | 672 |
rs768953025 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056932 | ACCTGTGTGAAAGTA[C/T]CTAGCACTGTGTATG | 672 |
rs768995134 | snp | C/T | 3.2956e-05 | 0.00405918 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092377 | TGGAGCCCACTTCAT[C/T]AGTACTGGAACCTAC | 672 |
rs769044421 | snp | A/G | 1.64939e-05 | 0.0028717 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093658 | TTCTACTGACTACTA[A/G]TTCAAGCGCATGAAT | 672 |
rs769088801 | in-del | -/ATT | 1.64798e-05 | 0.00287047 | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093302 | TTTGGGGTCTTCAGC[-/ATT]ATTAGACACTTTAAC | 672 |
rs769117682 | snp | A/C | 2.44663e-05 | 0.00349751 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124132 | TTTAACACATTAGAA[A/C]AACATATATATATAT | 672 |
rs769159611 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43078836 | CCACCCCCAATACAG[C/G]GTGATAATTGATAAA | 672 |
rs769213707 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099836 | TGTCCTCAGAGTTCT[C/T]ACAGTTCCAAGGTTA | 672 |
rs769253709 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115371 | GCCAAGCATGGTGGC[A/G]GGTGCCTGTAGTCCC | 672 |
rs769329522 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058810 | TGCACTAAAGAAAGT[G/T]AGAGGTTTTTCATAA | 672 |
rs769337190 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111878 | TAAAAAAAAGATTTC[A/G]GAACTTTAGGCTTGC | 672 |
rs769380445 | snp | A/G | 1.65567e-05 | 0.00287716 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093946 | GATTTATCATTTCAG[A/G]AGTCTTTTGAACTGC | 672 |
rs769394245 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096784 | TATTACTGTATATGA[A/G]GAACTTAGAGAACAA | 672 |
rs769456095 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092044 | TTTCAGCAAAACTAG[C/T]ATCTTCCTTTATTTC | 672 |
rs769483972 | snp | A/G | 1.65641e-05 | 0.00287781 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082373 | GAAAGAATTTTGCTT[A/G]AGATATCAGTGTTTG | 672 |
rs769549104 | snp | C/T | 1.8977e-05 | 0.00308028 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106544 | AAAATCTATAAATTA[C/T]AAAGAAAGAAAGAAC | 672 |
rs769566412 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074386 | GTGTGGCCCAGACTC[C/T]TCCAGCTGTTGCTCC | 672 |
rs769571683 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126231 | TTATTTTTCGGGTTC[A/G]GCTTGCTTTTGCCCC | 672 |
rs769589630 | snp | A/T | 3.29576e-05 | 0.00405928 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091499 | CGTTCCTCTTTCTTC[A/T]TCATCTGAAACCAAT | 672 |
rs769604075 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048883 | GTCACAGAGAGGAGG[G/T]GGAGGGACATATGGG | 672 |
rs769632909 | snp | A/G | 1.67184e-05 | 0.00289118 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045653 | TCTTGGGGTCCTGTG[A/G]CTCTGTACCTGTGGC | 672 |
rs769633464 | snp | C/G | 0.000185684 | 0.00963366 | splice-donor-variant, intron-variant, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125270 | CCCGGGACTCTACTA[C/G]CTTTACCCAGAGCAG | 672 |
rs769650474 | snp | G/T | 1.7911e-05 | 0.00299252 | BRCA1 | 17 | allele_origin=G(germline)/T(germline) | 17:43115727 | ACATTCAAACTTACT[G/T]GCAAAATATGTGGTC | 672 |
rs769678344 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088290 | ACTGAAATCTGCACT[C/T]ATCAAACAGTAACTC | 672 |
rs769682833 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102737 | AGCTCACTGTAGTCT[A/G]CATCTCCTGGACTCA | 672 |
rs769696827 | in-del | -/TC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107068 | CCAAGACAATTTTTT[-/TC]TTTTTTTTTTTTTTG | 672 |
rs769712441 | snp | A/G | 1.64779e-05 | 0.00287031 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092865 | TTCTTTAAGGACCCA[A/G]AGTGGGCAGAGAATG | 672 |
rs769734209 | snp | A/G | | | upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125518 | CAGAAAGAGCCAAGC[A/G]TCTCTCGGGGCTCTG | 672 |
rs769761849 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127011 | CAGCACTGCCGGCCC[A/G]CCTGCACCCCGCTTG | 672 |
rs769765263 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086651 | CAAGGACATTGTATA[C/T]TGAATGTCAAATATA | 672 |
rs769837854 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101266 | TGGTGGCGTGATCTC[A/G]GTTCACTGCAACCTC | 672 |
rs769895361 | snp | C/T | 3.58847e-05 | 0.00423569 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074552 | GAAGGAGAAAACCAT[C/T]GCCACCAATTGTGAA | 672 |
rs769948300 | in-del | -/AGAAACAGTTAAAGTGTCTAATAA | 1.64814e-05 | 0.00287061 | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093530 | TTACCTTCCATGAGT[-/AGAAACAGTTAAAGTGTCTAATAA]TGTAGGTTTCTGCTG | 672 |
rs770002293 | snp | A/C | 1.64912e-05 | 0.00287147 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093651 | CTTAGATTTCTACTG[A/C]CTACTAGTTCAAGCG | 672 |
rs770045451 | snp | G/T | 1.64727e-05 | 0.00286986 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057009 | GAGTGGAATACAGAG[G/T]GGTGGGGTGAGATTT | 672 |
rs770048742 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063202 | CCTGCATAATTCTTG[A/G]TGATCCTCATTATCA | 672 |
rs770055630 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067995 | AGACACCTGAAGTCT[C/T]GGCTGGGCGCGGTGG | 672 |
rs770090143 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094383 | CTGGAAAACCACTCA[C/T]TAACTTTCTGAATGC | 672 |
rs770132088 | snp | A/C | 3.56856e-05 | 0.00422392 | intron-variant | BRCA1 | GRCh38.p7 | 17:43094881 | AATATACAAAAATAA[A/C]AAGGTACTCAAAAAC | 672 |
rs770193975 | snp | A/C/T | 1.64727e-05 | 0.00286986 | BRCA1 | 17 | allele_origin=A(germline)/C(germline) | 17:43071020 | GCTTCTCCCTGCTCA[A/C/T]ACTTTCTTCCATTGC | 672 |
rs770202640 | in-del | -/A/TA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048533 | TTTTTTTTTTTTTTT[-/A/TA]AGACAAAGTCTCACT | 672 |
rs770271323 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108654 | GAGGTTGCAATGAGC[C/T]GAGAAGAGTGCCACT | 672 |
rs770279083 | snp | A/G | 3.29859e-05 | 0.00406102 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094223 | TATTAAAGCCTCATG[A/G]GGATCACTGGCCAGT | 672 |
rs770294549 | in-del | -/AT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100576 | ATATATATATAACAT[-/AT]ATATATAACATATAT | 672 |
rs770322547 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123038 | CTCCAGCCTGGGCAA[C/G]AGAGCAAGACTCCAT | 672 |
rs770326273 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106852 | ATTTCATGCTGCATA[A/G]TCAAATATAAACGGT | 672 |
rs770368390 | snp | A/C/G | 0.00037135 | 0.0136222 | intron-variant, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125258 | CCCTGTCCCTTTCCC[A/C/G]GGACTCTACTACCTT | 672 |
rs770377022 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055258 | TCATTGAGTCTTCTT[C/G]GGTCTCATCTGCAAA | 672 |
rs770433693 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114951 | ATACGTAAATATAAC[C/T]TGAATCACTGCTATA | 672 |
rs770460699 | in-del | -/A | 1.64811e-05 | 0.00287059 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093122 | AAATGCTGCACACTG[-/A]CTCACACATTTATTT | 672 |
rs770463722 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111284 | TGGCACTGTGGGAGG[C/T]CAAGGCGAGCAGATC | 672 |
rs770467165 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071463 | TTTCAGTCAACAATG[C/T]TAGTTTTAGAAATAT | 672 |
rs770514967 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076142 | GTGGTAAATCAACAG[C/T]TAGACTTTTTCTAGA | 672 |
rs770554414 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046182 | CCCACCTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 672 |
rs770579978 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091904 | CTCTTCTGAGGACTC[C/T]AATTTCTTGGCCCCT | 672 |
rs770583134 | snp | C/G | 1.64806e-05 | 0.00287054 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092842 | CAAAAGTGACTTTTG[C/G]ACTTTGTTTCTTTAA | 672 |
rs770596108 | in-del | -/TT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107062 | TAAATACCAAGACAA[-/TT]TTTTTTTTTTTTTTT | 672 |
rs770617294 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057335 | ACCAACATGGTGAAA[C/T]CTCATCTCTACTAAA | 672 |
rs770727938 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086524 | TTAGACGTAAGACAG[C/T]CTGAAATCTGACTTC | 672 |
rs770769275 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092700 | CCTCCTTTGATACTA[C/T]ATTTGGCATTATCAA | 672 |
rs770805378 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123656 | CTCGGCCTCATCCAT[A/G]ATTTTATTTTGCCAT | 672 |
rs770842236 | snp | C/T | 1.65255e-05 | 0.00287445 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093896 | ATTAGTAATATTCAT[C/T]ACTTGACCATTCTGC | 672 |
rs770872146 | snp | C/T | 3.32044e-05 | 0.00407444 | intron-variant | BRCA1 | GRCh38.p7 | 17:43105003 | GCAAGTGATTATCAA[C/T]CTTTTAAGGACACTA | 672 |
rs770894676 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116677 | GCGTGCGCCACCACG[A/C]CCGGCTGATTTTTCG | 672 |
rs770897278 | snp | A/G | 1.65553e-05 | 0.00287705 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099738 | ATAAGGAATCCAGCA[A/G]TTATTATTAAATACT | 672 |
rs770910897 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099729 | AACTATAAGATAAGG[A/G]ATCCAGCAATTATTA | 672 |
rs770929332 | in-del | -/TTTTT | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124746 | ACATACCAGCCGGTG[-/TTTTT]TGTTTTGTTTTGTTT | 672 |
rs770964634 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074994 | AAGGGAGGAAGGAAA[A/G]AAAGGAAGAAAGGAA | 672 |
rs771001707 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094655 | CATTCTGTCTTTAGT[A/G]AGTAATAAACTGCTG | 672 |
rs771008204 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060333 | AGGAATGAGCCACCA[A/C]ACCCAGCCGTGCCCA | 672 |
rs771076131 | snp | C/G | 4.95962e-05 | 0.00497952 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094727 | TGGCTCCACATGCAA[C/G]TTTGAAACAGAACTA | 672 |
rs771092891 | snp | A/G | 3.33178e-05 | 0.00408139 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051149 | AGAGAGAGGGACAGG[A/G]GAATGGAGAGAAGGA | 672 |
rs771121021 | in-del | -/AG | 0.000517102 | 0.0160712 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104080 | AAAAAGAAAAAAAAA[-/AG]AAAAGAAGAAGAAGA | 672 |
rs771137373 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070083 | GGATTATAGGCATGC[A/G]CCACCACGCCCGGCT | 672 |
rs771171482 | in-del | -/ACAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096664 | TTTATTATATAACAT[-/ACAG]ACAAAGCTTGAGAGA | 672 |
rs771183732 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105548 | ACCCTGCTGAGCTTA[C/T]TGTTCTTAACATCTG | 672 |
rs771194201 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066469 | AGGCTGGAGTGCAGT[A/G]GCAGGATCTCAGCTG | 672 |
rs771208553 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081745 | TCCTCAGCTCAGTGC[C/T]CACTTCTTATAGGAA | 672 |
rs771217677 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104517 | ACACTAAGAAATTTG[-/C]CTATCAATACTGTAT | 672 |
rs771235708 | in-del | -/AT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121762 | AAGCTAGAAAACATA[-/AT]AGTTGATTGAAAATA | 672 |
rs771237151 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119879 | CTGTAAACACAAACT[G/T]TGAACAGATGAAAAC | 672 |
rs771246729 | snp | C/T | 1.67877e-05 | 0.00289716 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082626 | TACTTTGAGAAGCTT[C/T]CCATTAAATGAAAAT | 672 |
rs771382888 | in-del | -/AAAAAAAAGAAAAGAAG | 0.000353794 | 0.0132956 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104073 | AAAAAAAAAAAAGAA[-/AAAAAAAAGAAAAGAAG]AAGAAGAAGAAGAAG | 672 |
rs771398886 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106586 | CTTCCTTTTGTAGAA[A/G]GAATACTCAAAAGGC | 672 |
rs771479616 | snp | C/T | 1.65002e-05 | 0.00287225 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092122 | CATGACTACTTCCCA[C/T]AGGCTGTTCTAAGTT | 672 |
rs771496487 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084152 | TCTTCTGCTTCAGCC[A/T]CCTGAGTAGCTGGGA | 672 |
rs771519405 | snp | A/C | 1.64795e-05 | 0.00287045 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093509 | CTTGGCTCCAGTTGC[A/C]GGTTCTTTACCTTCC | 672 |
rs771564275 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081169 | AATTGAAAGTCTAGT[C/T]TGTGTTTAGACTGAA | 672 |
rs771577266 | snp | C/T | 1.64727e-05 | 0.00286986 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43057070 | TCTGTCCTGGGATTC[C/T]CTTGCTCGCTTTGGA | 672 |
rs771582409 | snp | A/C | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125135 | CCCCAGGGTTCACAA[A/C]GCCTTACGCCTCTCA | 672 |
rs771594437 | snp | C/G | 1.65877e-05 | 0.00287986 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124002 | CCAAATTAATACACT[C/G]TTGTGCTGACTTACC | 672 |
rs771606902 | snp | C/T | 3.29522e-05 | 0.00405894 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045791 | CAGGTGCCTCACACA[C/T]CTGCCCAATTGCTGG | 672 |
rs771607637 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086230 | CTAATGCATTAGTAT[A/G]CCCAAATGGAACACA | 672 |
rs771614233 | in-del | -/TTTC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083163 | GAACCTTTAGTTTCT[-/TTTC]TTTCTTTCTTTCTTT | 672 |
rs771627806 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101084 | CCCCAGCACTCCTAA[C/G]AACATTTAGTATAGG | 672 |
rs771630271 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056519 | TATTATTGGCTGGGC[A/G]CGGTGGCTCACGCCT | 672 |
rs771761632 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069683 | GTGCACTTACTCATT[G/T]TATCTACCAGGGCAG | 672 |
rs771771029 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123282 | GTAATTTCATTGTAT[C/G]TACAGAGCCAGTTTC | 672 |
rs771810432 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108810 | CCAGCCTGACCAACA[C/T]GGAGAAACCCTGTCT | 672 |
rs771810795 | snp | C/T | 0.000580383 | 0.0170251 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044944 | GAGTAGCTGGGATTA[C/T]AGGTGTCCACCACCA | 672 |
rs771837028 | snp | C/G | 1.64893e-05 | 0.0028713 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094351 | GTGAGTCATCAGAAC[C/G]TAACAGTTCATCACT | 672 |
rs771837432 | in-del | -/A | 0.000296165 | 0.0121653 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045499 | GGAGACTTCAAGCAG[-/A]AAATCTTTAAGGGAC | 672 |
rs771865141 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109014 | AAAACAAAACAAAAC[-/A]AAAAAAACCCCAACT | 672 |
rs771879238 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097067 | AGTACCCGGATGATG[A/G]AAAAAATCTATACAC | 672 |
rs771883385 | in-del | -/AAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050615 | TCGACCTCAAAAAAA[-/AAG]AAGAAAAAAAAAAAG | 672 |
rs771887591 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43060167 | CCTCCACCTCCCGGG[C/T]TGATGAAGTGATTCT | 672 |
rs771890863 | snp | G/T | 1.65015e-05 | 0.00287237 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093675 | TCAAGCGCATGAATA[G/T]GCCTGGTAGAAGACT | 672 |
rs771892131 | snp | C/T | 1.64895e-05 | 0.00287132 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094202 | GTGAACTCTTTCACT[C/T]TTACATATTAAAGCC | 672 |
rs771909778 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074870 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 672 |
rs771968352 | in-del | -/ACAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052783 | CAGACGGACAGAAAC[-/ACAC]ACACACACACACACA | 672 |
rs771979902 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115165 | TTTCACTGATGGACA[C/T]AAAAAATACAAAACA | 672 |
rs771982743 | snp | A/T | 1.6507e-05 | 0.00287284 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097215 | TAGGAAAATACCAGC[A/T]TCATAGACAAAGGTT | 672 |
rs772024761 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099901 | CAGTATGGTAAAGAA[C/T]AGTCAAGCAATTGTT | 672 |
rs772031303 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113733 | GCCTATAATTTCCTT[A/C]TTCCACAAGTTCTCA | 672 |
rs772037778 | snp | C/G | 1.70255e-05 | 0.00291761 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124108 | CCATTTCTTTCTGTT[C/G]CAATGAACTTTAACA | 672 |
rs772058337 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096573 | AAGACCCCGTCTCCA[-/A]AAAAAAAAAAAAAAA | 672 |
rs772109504 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089965 | TGAACCATGACTGCA[C/T]TACTCCATTCCAGCC | 672 |
rs772130013 | snp | A/C | 1.6528e-05 | 0.00287467 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104983 | TTGTTTGAGAAACAC[A/C]CTCAGCAAGTGATTA | 672 |
rs772131942 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106380 | ATGGTTTTATAGGAA[C/T]GCTATGTTATTAAAT | 672 |
rs772136430 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073601 | AAAGTGATTTTTAAG[A/G]CATAAAATATGTAGT | 672 |
rs772186923 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105393 | TATGGGCATATGCCA[A/C]CATGTACATTTATTT | 672 |
rs772215665 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125216 | ATCCACTCTCCCACG[C/T]CAGTACCCCAGAGCA | 672 |
rs772224921 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051011 | CTTATAATACTCCAC[A/T]ATGTAAGACAAAGGC | 672 |
rs772226744 | snp | C/G | 1.68476e-05 | 0.00290233 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106506 | TGAAGGCCCTTTCTT[C/G]TGGTTGAGAAGTTTC | 672 |
rs772245946 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072370 | CTCCAGCCTGGGCAA[C/T]AAGAGTGAAACTCCG | 672 |
rs772281432 | snp | G/T | 1.65282e-05 | 0.00287469 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082385 | CTTAAGATATCAGTG[G/T]TTGGCCAACAATACA | 672 |
rs772295194 | snp | A/G | 0.000151114 | 0.00869105 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045493 | TCCAAGGGAGACTTC[A/G]AGCAGAAAATCTTTA | 672 |
rs772296606 | snp | A/G | 3.33533e-05 | 0.00408357 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091396 | TTAGCTCACTTCTAT[A/G]AATAGACTGGGGCAA | 672 |
rs772311203 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066329 | TCGGAGCTGTTATCA[G/T]ACTTTTTTCCTGAAA | 672 |
rs772383323 | snp | A/G | 1.65108e-05 | 0.00287317 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092174 | GAAATCTGTATTAAC[A/G]GTCTGAACTACTTCT | 672 |
rs772467758 | in-del | -/A/AA | 0.575237 | 0.160195 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110587 | GTAAGACCCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 672 |
rs772468999 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118156 | GTAAAGAAACACACT[A/G]TGCAACAATTAGGGG | 672 |
rs772578738 | snp | A/C | 1.64868e-05 | 0.00287109 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076467 | CAGATACCACAGCAT[A/C]TTTACATTGATGTTT | 672 |
rs772583635 | snp | C/G | 1.64765e-05 | 0.00287019 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099768 | TTAAAAAACCTGAGA[C/G]CCTTACCCAATTCAA | 672 |
rs772616764 | snp | A/G | 3.31543e-05 | 0.00407137 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051055 | CTGGGGTTCTCCCAG[A/G]CTCTTACCTGTGGGC | 672 |
rs772617029 | snp | A/C | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093262 | TTTCAGTTTGCAAAA[A/C]CCTTTCTCCACTTAA | 672 |
rs772644046 | in-del | -/TAT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059899 | CCAGCTACACTGGCC[-/TAT]TATTATTATTATTAT | 672 |
rs772684048 | snp | C/T | 0.000131833 | 0.00811782 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094647 | TCTACATTCATTCTG[C/T]CTTTAGTGAGTAATA | 672 |
rs772703445 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091716 | GCCAATATTACCTGG[C/T]TACTGCAGTCATTTA | 672 |
rs772731581 | in-del | -/A/AA/AAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067890 | ACCCAGGCTGGAGGT[-/A/AA/AAA]AAAAAAAAAAAAAAA | 672 |
rs772754015 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068601 | TATTAATTTTGCTTT[A/T]ATAGCAGATATCATT | 672 |
rs772759939 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091808 | GGTGCTATGCCTAGT[A/G]GACTGAGAAGGTATA | 672 |
rs772761024 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108917 | AGAATCTCTTGAACC[C/T]GGGAGGCGGAGGTTG | 672 |
rs772786896 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055804 | TAGTTGTTGTGGCAC[A/G]TGCCTGTAATCCTAG | 672 |
rs772846663 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075771 | CTACATAGTCCAGTA[C/T]TGGACTGCTATACAG | 672 |
rs772854836 | snp | C/T | 4.96069e-05 | 0.00498006 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092552 | CAGATTTTTCTTACA[C/T]TTAGTTTTAACAAAT | 672 |
rs772874662 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069945 | GCAATTCTTCTTCTT[A/C]TTATTGAGACAGAGT | 672 |
rs772876836 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054217 | ACTGGCTCACATGGC[A/G]CTCCCCTGTGGTAAA | 672 |
rs772885662 | snp | G/T | 1.6582e-05 | 0.00287936 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063911 | TCCTCCCGCAATTCC[G/T]AGAAAATATTTCAGT | 672 |
rs772888465 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110112 | TGTTAGCCAGGATGG[C/T]CTCGATCTCCTGACC | 672 |
rs772893671 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43045917 | GATTAATGAGGTAGA[A/G]GCTAATTTTTTTTTT | 672 |
rs772934225 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127021 | GGCCCGCCTGCACCC[C/T]GCTTGAATTCTCACC | 672 |
rs772960140 | snp | C/T | 1.64806e-05 | 0.00287054 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093110 | CTTGGGGTTTTCAAA[C/T]GCTGCACACTGACTC | 672 |
rs772975110 | snp | G/T | 1.6516e-05 | 0.00287362 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093754 | ATTCGAGTTCCATAT[G/T]GCTTATACTGCTGCT | 672 |
rs773013395 | snp | C/T | 1.64817e-05 | 0.00287064 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43093008 | TTCTATGCTTGTTTC[C/T]CGACTGTGGTTAACT | 672 |
rs773082120 | snp | C/G | 1.67492e-05 | 0.00289384 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063406 | AAGACAGGTTACATA[C/G]AGCAGAAGAACGTGC | 672 |
rs773082670 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115181 | AAAAAATACAAAACA[C/T]TGTTCAAAATGATGT | 672 |
rs773119778 | snp | A/G | 0.003908 | 0.044031 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044965 | TCCACCACCATGACC[A/G]GCTAATTTCTGTATT | 672 |
rs773139281 | snp | A/G | 3.30055e-05 | 0.00406222 | intron-variant | BRCA1 | GRCh38.p7 | 17:43097228 | GCTTCATAGACAAAG[A/G]TTCTCTTTGACTCAC | 672 |
rs773188144 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084177 | CTGGGATTACAGGCG[A/C]CCGCCACCATGCCCA | 672 |
rs773189986 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121841 | GTTTTTAATTGATGG[C/T]TTAATTTGCCAGAAT | 672 |
rs773212667 | snp | G/T | 3.30349e-05 | 0.00406403 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093676 | CAAGCGCATGAATAT[G/T]CCTGGTAGAAGACTT | 672 |
rs773244301 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047167 | TACAGTGGTGTGATC[C/G]TGGCTCACTGAAGCA | 672 |
rs773286567 | in-del | -/AA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073382 | GAGATGTCATCCTTG[-/AA]ACATTTCAGAAAATG | 672 |
rs773332235 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090261 | TGCAGTAGGCATATT[C/G]TTAAAATGGAGCTAT | 672 |
rs773413634 | in-del | -/CT | 1.6483e-05 | 0.00287076 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093553 | TTCTGCTGTGCCTGA[-/CT]GGCATTTGGTTGTAC | 672 |
rs773425863 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059248 | GTGGGTGGATTACCT[A/G]AGGTCAGGAGTTTAA | 672 |
rs773433679 | snp | C/G | 0.000115309 | 0.00759218 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094555 | TATCATTACATGTTT[C/G]CTTACTTCCAGCCCA | 672 |
rs773456796 | snp | A/G | 1.66421e-05 | 0.00288458 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091322 | TTTCAAGTTTAAGAA[A/G]CAGTTCCTTTAACTA | 672 |
rs773481086 | snp | A/G | 0.00014707 | 0.00857398 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045500 | GAGACTTCAAGCAGA[A/G]AATCTTTAAGGGACC | 672 |
rs773489058 | snp | C/T | 1.65627e-05 | 0.00287769 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104997 | CACTCAGCAAGTGAT[C/T]ATCAACCTTTTAAGG | 672 |
rs773524529 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071145 | GATGGTATGTTGCCA[A/G]CACGAGCTGACTCTG | 672 |
rs773613294 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119627 | TAACTTGTACCAACA[C/T]TGGTATTATTACTGG | 672 |
rs773630860 | snp | A/G | 2.45348e-05 | 0.0035024 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091057 | CAAAAACAGAGGTTC[A/G]GATGTAAAAGCAGAC | 672 |
rs773638815 | snp | C/T | 3.29804e-05 | 0.00406068 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092100 | GTCTCAGAACAAACC[C/T]GAGATGCATGACTAC | 672 |
rs773647432 | in-del | -/CTAT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088242 | GTGTTACCATTGCCA[-/CTAT]CTATCTCCAGAACTT | 672 |
rs773655919 | snp | A/C | 4.97269e-05 | 0.00498608 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051056 | TGGGGTTCTCCCAGG[A/C]TCTTACCTGTGGGCA | 672 |
rs773675561 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105424 | ATTTATTTTGTTGGT[A/G]GTGATGGGGTCTCAC | 672 |
rs773709174 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091542 | AGACCAACTCCCTGG[C/T]TTTCAGACTGATGCC | 672 |
rs773776207 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079786 | CATGGCATAATAGGT[A/G]TTAAAAAAAAAAAAA | 672 |
rs773776280 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119245 | GCCAAGGCGGGCCAG[-/C]CTGGGTGACAGAGAA | 672 |
rs773821829 | snp | A/C | 1.66499e-05 | 0.00288525 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067711 | CTGAAATTAAATCAA[A/C]TATTCCATTATCATG | 672 |
rs773841328 | snp | C/T | 1.79945e-05 | 0.00299949 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115774 | GGTTCCTTGATCAAC[C/T]CCAGACTAGCAGGGT | 672 |
rs773857297 | in-del | -/TA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076306 | TCTCATGTTGTAGCT[-/TA]TGTTATAGGTTCAAA | 672 |
rs773880385 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065036 | GGGGTTTCACCGTGT[A/T]AGCCAGGATGGTCTC | 672 |
rs773898225 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081957 | TTTCTGTGGATCAAA[A/G]TGCAGTTCCTGAAGT | 672 |
rs773906023 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075060 | GAGGGAAAGGAAAGG[-/A]AAGGACGGAAGGAAG | 672 |
rs773937268 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43068003 | GAAGTCTCGGCTGGG[C/T]GCGGTGGCTCACGCC | 672 |
rs773952371 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112282 | TTTAGTAGAGATGGT[A/G]TTACCATATTGGCCA | 672 |
rs773962435 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120529 | CCAGCACTTTGGGAG[A/G]CCGAGGTGGGCGGAT | 672 |
rs774127304 | snp | A/G | 3.3112e-05 | 0.00406877 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43045684 | TGGCTGCAGTCAGTA[A/G]TGGCTGTGGGGGATC | 672 |
rs774159828 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094074 | TGTGGCTCAGTAACA[A/G]ATGCTCCTATAATTA | 672 |
rs774200603 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121455 | TTTCGGAGGCCAAGG[C/T]AGGAGGATCACCTGA | 672 |
rs774226893 | snp | C/T | 3.29837e-05 | 0.00406088 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076437 | ACAATCAGAGTTCAA[C/T]ATAAATAAAGATGTC | 672 |
rs774284145 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095866 | TTTGCAGAATCCAAA[A/C]TGATTTCATCCCTGG | 672 |
rs774296138 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044806 | TAGTTTCATTTTCCT[-/TT]TTTTTTTTTTTTTTT | 672 |
rs774309689 | in-del | -/AAAACAAAAC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108995 | CGAAACTCCATCTCA[-/AAAACAAAAC]AAAACAAAACAAAAA | 672 |
rs774339888 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096939 | GATGATCTCTAAGGT[G/T]TCTTCCAATACCATG | 672 |
rs774365187 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049324 | CTGTCTCTCTGCTCC[A/G]AAGGACAATGGTCTT | 672 |
rs774368374 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113662 | GTGAGCCACCGCGCC[C/T]GTCCTCTATTTTCTT | 672 |
rs774408406 | in-del | -/TC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121821 | TTTAATTTTTATGTA[-/TC]TGAGTTTTTAATTGA | 672 |
rs774424435 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089922 | TGAGGTAGGAGGATC[A/G]CTTGAGCCCAGGAAG | 672 |
rs774452090 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067659 | TTAGATTAGTTAAAG[A/T]GATGTGGTGTTTTCT | 672 |
rs774453086 | in-del | -/G | 0.000560412 | 0.01673 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104081 | AAAAGAAAAAAAAAA[-/G]AAAAGAAGAAGAAGA | 672 |
rs774467462 | snp | C/T | 3.2987e-05 | 0.00406108 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104835 | TTTCATGGACAGCAC[C/T]TGAGTGTCATTCTTG | 672 |
rs774476213 | in-del | -/TTT/TTTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067836 | ACTATTTAAAGTGAA[-/TTT/TTTT]TTTTTTTTTTTTTTT | 672 |
rs774505084 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071035 | CACTTTCTTCCATTG[C/T]ATTATACCCAGCAGT | 672 |
rs774553547 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063776 | CTTTTGGTAACTCAG[A/C]CTCAGCATCAGCAAA | 672 |
rs774583925 | snp | A/T | 8.23649e-05 | 0.00641683 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104194 | CATACTTTGGATGAT[A/T]GAAACTTCATCTTTT | 672 |
rs774593602 | snp | C/G/T | 2.01534e-05 | 0.00317432 | BRCA1 | 17 | allele_origin=G(germline)/C(germline) | 17:43091018 | TTTCACTCTCACACC[C/G/T]AGATGCTGCTTCACC | 672 |
rs774617298 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072037 | ATAAAAATAAATAAA[C/T]AAATAAAAGTTTATG | 672 |
rs774637480 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088769 | TTTTAAGAATGTGCC[C/T]ACGGCAGGTCAGAGA | 672 |
rs774644946 | snp | C/T | 1.65168e-05 | 0.00287369 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092528 | ATGTTCCTCAAAGTT[C/T]TCCTCTAGCAGATTT | 672 |
rs774646943 | snp | A/C | 5.23464e-05 | 0.00511571 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090928 | ACGCATGTGCACACA[A/C]ACACACGCTTTTTAC | 672 |
rs774666969 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063436 | CTCTTTTCACGGAGA[C/T]AGAGAGGTCAGCGAT | 672 |
rs774679104 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091834 | GTATATTGTTTACTT[C/T]ACCAAATAACAAGTG | 672 |
rs774730386 | snp | A/C | 1.64827e-05 | 0.00287073 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093159 | GTTTTTGCCTTCCCT[A/C]GAGTGCTAACTTCCA | 672 |
rs774731955 | snp | A/T | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124357 | CCTTGGGTCTTTTCC[A/T]TTCTCCAAGAAAGAG | 672 |
rs774753108 | in-del | -/CACACACACACACACT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052810 | ACACACACACACACA[-/CACACACACACACACT]CTCTTACTTTACCGC | 672 |
rs774785050 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087554 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 672 |
rs774799138 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087682 | AAAAAAAAAAAAAAA[-/G]AAAAAAGAATTTTAA | 672 |
rs774813458 | snp | A/G | 1.65869e-05 | 0.00287979 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051044 | GTGCTGGAACTCTGG[A/G]GTTCTCCCAGGCTCT | 672 |
rs774813954 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079468 | GAATGCCCCACAAGT[G/T]TTACCATGGCAAAAC | 672 |
rs774837285 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118012 | ATACATGGGAATAAG[A/T]GCATTAAAGAGAAAA | 672 |
rs774839252 | snp | C/G | 0.000185753 | 0.00963545 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125280 | TACTACCTTTACCCA[C/G]AGCAGAGGGTGAAGG | 672 |
rs774849810 | snp | A/G | 0.000148257 | 0.00860851 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094544 | GGGAGTCCGCCTATC[A/G]TTACATGTTTCCTTA | 672 |
rs774888483 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117175 | GGCCGGGCATGGTGC[C/T]TCATGCCTGTAATCC | 672 |
rs774892235 | snp | C/T | 5.83311e-05 | 0.0054002 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124137 | CACATTAGAAAAACA[C/T]ATATATATATCTTTT | 672 |
rs774929272 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095699 | CAGACCATACCACGA[C/G]ATTTGACAGAGAATG | 672 |
rs774944967 | snp | C/T | 3.31027e-05 | 0.0040682 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082377 | GAATTTTGCTTAAGA[C/T]ATCAGTGTTTGGCCA | 672 |
rs774947869 | in-del | -/AA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050619 | ACCTCAAAAAAAAAG[-/AA]AAAAAAAAAGAAATG | 672 |
rs774959350 | snp | C/T | 1.65605e-05 | 0.0028775 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093951 | ATCATTTCAGGAGTC[C/T]TTTGAACTGCCAAAT | 672 |
rs774983954 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43056668 | ATGGAGTGAGACTCC[A/G]TCTTGGGAAAAAAAA | 672 |
rs774988515 | in-del | -/T | 1.65135e-05 | 0.00287341 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049136 | TGTGCCAAGGGTGAA[-/T]GATGAAAGCTCCTTC | 672 |
rs775014430 | snp | C/T | 1.64849e-05 | 0.00287092 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099762 | AAATACTTAAAAAAC[C/T]TGAGACCCTTACCCA | 672 |
rs775032066 | snp | C/T | 0.000115336 | 0.00759305 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43094061 | CTCTTGTATTATCTG[C/T]GGCTCAGTAACAAAT | 672 |
rs775090053 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43099335 | GAGTGCAATGGTGCG[A/T]TCTCGGTTCACCGCA | 672 |
rs775110369 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125561 | AGTCTGCCCCCGGAT[A/G]ACGTAAAAGGAAAGA | 672 |
rs775125813 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096792 | TATATGAGGAACTTA[G/T]AGAACAATCTGCTAG | 672 |
rs775205445 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050617 | GACCTCAAAAAAAAA[-/G]GAAAAAAAAAAAGAA | 672 |
rs775235695 | snp | A/G | 1.68786e-05 | 0.002905 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063956 | AAACTCAGCATCTGC[A/G]GAATGAAAAACACTC | 672 |
rs775274813 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120220 | TACAAAGAACTACCA[A/G]TTGTCAGAAATAGCT | 672 |
rs775339017 | snp | A/T | 1.64776e-05 | 0.00287028 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091503 | CCTCTTTCTTCATCA[A/T]CTGAAACCAATTCCT | 672 |
rs775348455 | snp | C/T | 5.50413e-05 | 0.00524573 | intron-variant, missense | BRCA1 | GRCh38.p7 | 17:43079340 | GAGAGGCACCTGATA[C/T]ATGTTCTCTAGGCCT | 672 |
rs775406185 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111948 | TTATCCGTAGAAAAT[A/G]CAATTAATACAACAA | 672 |
rs775417240 | in-del | -/TGGGGGATC | 0.000149183 | 0.00863536 | BRCA1 | 17 | allele_origin=C(germline)/(germline) | 17:43045691 | AGTCAGTAGTGGCTG[-/TGGGGGATC]TGGGGTATCAGGTAG | 672 |
rs775424259 | snp | C/G | 1.64871e-05 | 0.00287111 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093433 | CATTTGTTAACTTCA[C/G]CTCTGGGAAAGTATC | 672 |
rs775430301 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067770 | CTAGTTATTCCACCA[C/T]GGCATATGTTTACCT | 672 |
rs775434420 | in-del | -/AAA/AACAAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059513 | AACAACAACAACAAC[-/AAA/AACAAA]AAATTCTCACATCTA | 672 |
rs775435619 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057510 | AGCGAGACTCCATCT[C/T]GCATCTCAAAAAATT | 672 |
rs775459363 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110313 | AAATACTGGCCAGGC[A/G]TGATGACTCACACCT | 672 |
rs775463394 | snp | C/T | 1.64893e-05 | 0.0028713 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091447 | TACCTAAGTTTGAAT[C/T]CATGCTTTGCTCTTC | 672 |
rs775473207 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088523 | CAGTTAACACAATGT[C/T]TTCAAGGTTCGTCCA | 672 |
rs775477245 | snp | A/G | 1.65029e-05 | 0.00287248 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094694 | CTGTAATGAGCTGGC[A/G]TGAGTATTTGTGCCA | 672 |
rs775491638 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103116 | GTGACCTTATGGCTA[C/T]TTTAGATAAGCATCA | 672 |
rs775525479 | snp | A/G | 1.94759e-05 | 0.00312051 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106549 | CTATAAATTATAAAG[A/G]AAGAAAGAACAATTT | 672 |
rs775546213 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102820 | ACCATGCCCAGATAA[C/T]TTAAAAAAACTTTTA | 672 |
rs775576268 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117044 | CACTTTACAGATGGT[A/C]CTGTGTACTCTTATT | 672 |
rs775618857 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43049229 | GTAAAATCACTGCAG[G/T]AATCTGCATACTTAA | 672 |
rs775669794 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126820 | GAGCCGGCTCCCTCT[A/G]CTTGCGGGGAAGTGT | 672 |
rs775676944 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057602 | GGACTTTGGGAGGCC[A/G]AGACAGGCGGATCAC | 672 |
rs775708612 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047443 | CATATCTTACTCCCA[C/T]CCCATGGAAACAGTT | 672 |
rs775749052 | in-del | -/AAG | 0.0185599 | 0.0945276 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104083 | AGAAAAAAAAAAGAA[-/AAG]AAGAAGAAGAAGAAG | 672 |
rs775791214 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101409 | ACCACATTGCCTAGG[C/T]TGGTCTTGAACTCTA | 672 |
rs775837744 | snp | A/G | 6.58903e-05 | 0.00573941 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071116 | ATTGGGGAACTTTCA[A/G]TGCAGAGGTTGAAGA | 672 |
rs775847208 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086700 | AGATGTAATCAGAAA[C/T]TGCAACCTTAAACTT | 672 |
rs775850331 | snp | A/G/T | 3.61202e-05 | 0.00424959 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074553 | AAGGAGAAAACCATC[A/G/T]CCACCAATTGTGAAA | 672 |
rs775851068 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115804 | TAGGGGGGGAGAAAA[A/C]GAAAATAAATGAGGC | 672 |
rs775869160 | snp | A/G | 3.29924e-05 | 0.00406142 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094245 | CTGGCCAGTAAGTCT[A/G]TTTTCTCTGAAGAAC | 672 |
rs775885098 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092201 | TTCTTCATATTCTTG[C/T]TTTTTTATTTCAGGA | 672 |
rs775926635 | snp | A/G/T | 1.64928e-05 | 0.00287161 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090918 | CACCACACACACGCA[A/G/T]GTGCACACACACACA | 672 |
rs775967490 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43053033 | AGGTGCACACCACCA[C/T]ACCCGGCTAATTTTT | 672 |
rs775978427 | snp | C/T | 1.70081e-05 | 0.00291612 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104307 | GCAGTTAGAGAAAAA[C/T]GTATGAATTATAATC | 672 |
rs776015621 | snp | A/C | 3.29826e-05 | 0.00406082 | intron-variant | BRCA1 | GRCh38.p7 | 17:43070880 | AAAACTCTTTCCAGA[A/C]TGTTGTTAAGTCTTA | 672 |
rs776018348 | snp | A/G | 1.6834e-05 | 0.00290116 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063418 | ATACAGCAGAAGAAC[A/G]TGCTCTTTTCACGGA | 672 |
rs776038233 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43108575 | CCAGGCGTGGTGGGC[A/C]CACGCCTGAGTCCCA | 672 |
rs776068983 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075255 | ACATCTCTACACTCA[C/T]TCTTTCTACTCAGTT | 672 |
rs776070899 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091679 | TGTTTCCTCACTAAG[A/G]TGATGTTCCTGAGAT | 672 |
rs776085861 | in-del | -/CC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052818 | CACACACACACACAC[-/CC]ACACACTCTCTTACT | 672 |
rs776115545 | snp | C/T | 1.65091e-05 | 0.00287303 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093785 | TATAGGTTCAGCTTT[C/T]GTTTTGAAAGCAGAT | 672 |
rs776167818 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057371 | AAAAAATTAGTTGGG[C/T]GTGGTGGCAGGCACC | 672 |
rs776177740 | snp | C/G | 1.95927e-05 | 0.00312985 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43124124 | CAATGAACTTTAACA[C/G]ATTAGAAAAACATAT | 672 |
rs776203826 | snp | C/T | 3.31098e-05 | 0.00406864 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099739 | TAAGGAATCCAGCAA[C/T]TATTATTAAATACTT | 672 |
rs776214198 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055871 | TTTGAACTTGGGAGG[C/T]GAAGGTTGCAGTGAG | 672 |
rs776235719 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43107054 | CAACAATAATAAATA[C/T]CAAGACAATTTTTTT | 672 |
rs776270258 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091429 | ACAAAAACCTGGTTC[C/T]AATACCTAAGTTTGA | 672 |
rs776278453 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094578 | CCAGCCCATCTGTTA[C/T]GTTGGCTCCTTGCTA | 672 |
rs776303574 | snp | A/C | 1.83849e-05 | 0.00303185 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079331 | GGGAAAGAGGAGAGG[A/C]ACCTGATATATGTTC | 672 |
rs776316151 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103634 | CTGTAAGGTCTCTCT[C/T]TTGATTATATCAGGT | 672 |
rs776323117 | snp | C/T | 1.64999e-05 | 0.00287222 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049147 | TGAATGATGAAAGCT[C/T]CTTCACCACAGAAGC | 672 |
rs776323505 | snp | C/T | 0.000185118 | 0.00961898 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045647 | GCTCATTCTTGGGGT[C/T]CTGTGGCTCTGTACC | 672 |
rs776355028 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43047327 | CTGGTCTCGAACTTC[C/T]AGGCTCCCACCTTGA | 672 |
rs776357552 | snp | A/C | 3.29891e-05 | 0.00406122 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076635 | AATGGAATGAGAAAA[A/C]AAATCTACTTTACTG | 672 |
rs776362840 | in-del | -/TACTT | 3.2993e-05 | 0.00406145 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076641 | ATGAGAAAACAAATC[-/TACTT]TACTGCTTTGTTCTG | 672 |
rs776414807 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079061 | AAAAATTAGCTGGGC[A/G]TGGTGGCGGGTGCCT | 672 |
rs776446166 | in-del | -/AAGAA | 0.000108149 | 0.00735274 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104087 | AAAAAAAAAGAAAAG[-/AAGAA]GAAGAAGAAGAAGAA | 672 |
rs776483189 | in-del | -/ACA/ACAACG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059514 | ACAACAACAACAACA[-/ACA/ACAACG]AATTCTCACATCTAA | 672 |
rs776489394 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106119 | GCAGGACCCTGTCTT[-/A]AAAAAAAAAAAAAAA | 672 |
rs776512377 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092709 | ATACTACATTTGGCA[C/T]TATCAACTGGCTTAT | 672 |
rs776540382 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125313 | TCCTGAGCGCAGGGG[C/T]CCAGTTATCTGAGAA | 672 |
rs776542749 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093515 | TCCAGTTGCAGGTTC[C/T]TTACCTTCCATGAGT | 672 |
rs776568544 | snp | G/T | 1.65291e-05 | 0.00287476 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092587 | TGATGGGAAAAAGTG[G/T]TGGTATACGATATGG | 672 |
rs776594341 | snp | A/G | 1.6566e-05 | 0.00287797 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091080 | AAGCAGACTATAAAC[A/G]CTGCAACTTGCTGTG | 672 |
rs776607293 | snp | A/G | 1.91068e-05 | 0.0030908 | intron-variant | BRCA1 | GRCh38.p7 | 17:43106418 | ACTTTTTCCTACTGT[A/G]GTTGCTTCCAACCTA | 672 |
rs776610841 | snp | A/C | 0.000299476 | 0.0122331 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045552 | TTCAGGCTGATGTAC[A/C]TAAAATATTTAGTAG | 672 |
rs776615007 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070155 | TCAGGCTGGTCTTGA[G/T]CTCCTGACCTTAGGT | 672 |
rs776619391 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084511 | AGAAGGAACAGCAAT[A/G]GTTGCCAAAAAGTCC | 672 |
rs776621395 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101257 | GCTGGAGCGTGGTGG[A/C]GTGATCTCGGTTCAC | 672 |
rs776624908 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109026 | AAACAAAAAAACCCC[A/T]ACTATATCTATATCT | 672 |
rs776715199 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126889 | GCGCTCGCCAGCCAG[C/T]GCGAGTTCCAGGTGG | 672 |
rs776782462 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113809 | CAGGGTCAGCCAGGC[A/G]CGGTGGCTTACACCT | 672 |
rs776813709 | snp | A/G | 0.000388727 | 0.013936 | utr-variant-5-prime, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125352 | GCCTGTCCCCCGTCC[A/G]GGAAGTCTCAGCGAG | 672 |
rs776854280 | snp | A/G | 3.35098e-05 | 0.00409314 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051162 | GGGGAATGGAGAGAA[A/G]GAAAATCTAGTTATA | 672 |
rs776865875 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076735 | AAATTGGTTTTTAAA[C/G]AAGTATATCAGGCAG | 672 |
rs776992058 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43105553 | GCTGAGCTTACTGTT[A/C]TTAACATCTGAACCC | 672 |
rs776992322 | snp | A/G | 1.67956e-05 | 0.00289784 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067731 | CCATTATCATGAGTT[A/G]CCTCTAGCACACAGC | 672 |
rs776996813 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091650 | TGTGAAGAAAACAAG[C/G]TAGCAGAACATTTTG | 672 |
rs776999497 | snp | C/T | 1.64846e-05 | 0.0028709 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094665 | TTAGTGAGTAATAAA[C/T]TGCTGTTCTCATGCT | 672 |
rs777009084 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099891 | TCCTGCTAAACAGTA[C/T]GGTAAAGAACAGTCA | 672 |
rs777057839 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082510 | CCCATGCTGTTCTAA[C/T]ACAGCTTCTAGTTCA | 672 |
rs777091166 | snp | A/C | 1.66128e-05 | 0.00288204 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049219 | ACATTTAGATGTAAA[A/C]TCACTGCAGTAATCT | 672 |
rs777102216 | snp | A/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104140 | GGAAGGATTTTCGGG[A/T]TCACTCTGTAGAAGT | 672 |
rs777132211 | snp | C/G | 1.64928e-05 | 0.00287161 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094215 | CTTTTACATATTAAA[C/G]CCTCATGAGGATCAC | 672 |
rs777163785 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43076628 | TGCTTTAAATGGAAT[C/G]AGAAAACAAATCTAC | 672 |
rs777191440 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43086242 | TATACCCAAATGGAA[C/T]ACATGACCTTGATAG | 672 |
rs777209959 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054040 | AGAGAAAAATACTAT[A/G]GTGACATTTAGTATT | 672 |
rs777228325 | snp | A/G | 4.94254e-05 | 0.00497094 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43094112 | AGTTACATGGCTTAA[A/G]TTGGGGAGGCTTGCC | 672 |
rs777260550 | snp | C/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126070 | GACTACAATTCCCAT[C/G]CAGCCCCAGGAGTCT | 672 |
rs777262055 | snp | C/T | 3.45578e-05 | 0.00415665 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124112 | TTCTTTCTGTTCCAA[C/T]GAACTTTAACACATT | 672 |
rs777297026 | snp | A/G | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071174 | TGGGGCTCTGTCTTC[A/G]GAAGGATCAGATTCA | 672 |
rs777297771 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052614 | TATGTTTTGGGTGAC[C/T]CTCAGTGTCTTGACC | 672 |
rs777305766 | snp | A/T | 1.64871e-05 | 0.00287111 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094356 | TCATCAGAACCTAAC[A/T]GTTCATCACTTCTGG | 672 |
rs777371808 | snp | A/G | 1.65201e-05 | 0.00287398 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049133 | TACTGTGCCAAGGGT[A/G]AATGATGAAAGCTCC | 672 |
rs777371832 | in-del | -/TA | 1.64754e-05 | 0.00287009 | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091819 | AGTAGACTGAGAAGG[-/TA]TATATTGTTTACTTT | 672 |
rs777404687 | snp | A/G | 3.29576e-05 | 0.00405928 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093197 | GATACTTTCCTGAGT[A/G]CCATAATCAGTACCA | 672 |
rs777491912 | snp | A/C/T | 3.29697e-05 | 0.00406005 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43104911 | ACAAATGATTTTCAA[A/C/T]AGCTCTTCAACAAGT | 672 |
rs777503339 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062927 | TGGAGTTTTGCTCTT[G/T]TTGCCCAGGTTAGAG | 672 |
rs777508920 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114174 | CTGGCCTTAAGTGAT[C/T]TTCCTGCCTTGGCCT | 672 |
rs777515082 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099811 | TCTTTTGAGGTTGTA[G/T]CCGCTGCTTTGTCCT | 672 |
rs777531326 | in-del | -/TTG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082186 | CCCCATAGCATCTAC[-/TTG]TTGTAGGTACTCAGA | 672 |
rs777558172 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117985 | GGTAGACAGTTGATA[C/T]GGAATTAAAGAATAC | 672 |
rs777560742 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43101135 | ACATTACTTTTTTTT[C/T]CCTTCCTTTTTAGCT | 672 |
rs777595821 | snp | A/G | 1.6525e-05 | 0.00287441 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093881 | ATTCTCATGACCACT[A/G]TTAGTAATATTCATC | 672 |
rs777639827 | snp | A/G | 1.65674e-05 | 0.00287809 | intron-variant | BRCA1 | GRCh38.p7 | 17:43099730 | ACTATAAGATAAGGA[A/G]TCCAGCAATTATTAT | 672 |
rs777655282 | snp | C/G | 1.8104e-05 | 0.0030086 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079430 | AATTGTAGACATCAA[C/G]GGAACGGGTACTGTT | 672 |
rs777686976 | in-del | -/TA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100526 | GTGTGTGTGTGTGTA[-/TA]TATATATATACATAT | 672 |
rs777691131 | snp | A/G | 0.00018558 | 0.00963098 | intron-variant, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43125184 | CGTCAAAGAATACCC[A/G]TCTGTCAGCTTCGGA | 672 |
rs777695408 | in-del | -/TTTT | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044805 | CTAGTTTCATTTTCC[-/TTTT]TTTTTTTTTTTTTTT | 672 |
rs777770947 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122770 | ATACAAGAATGGCTG[A/G]ACGCAGTGGCTTATG | 672 |
rs777796838 | snp | C/T | 1.64974e-05 | 0.00287201 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092005 | CGCTTTTGCTAAAAA[C/T]AGCAGAACTTTCCTT | 672 |
rs777828258 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067672 | AGTGATGTGGTGTTT[C/T]CTGGCAAACTTGTAC | 672 |
rs777829292 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117662 | GAGAATCGCTTGAAC[C/T]GGGGAAGTGCACGTT | 672 |
rs777885366 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106419 | CTTTTTCCTACTGTG[A/G]TTGCTTCCAACCTAG | 672 |
rs777903680 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115677 | TCCTGGGTTATGAAG[A/G]ACAAAAACAAAAGCT | 672 |
rs777916645 | snp | A/T | 1.65244e-05 | 0.00287436 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094003 | CAGGATGAAGGCCTG[A/T]TGTAGGTCTCCTTTT | 672 |
rs777922080 | in-del | -/GTC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051882 | CCTCGTGATCTGCCT[-/GTC]TTGGCCTTCCAAAGT | 672 |
rs777938968 | snp | C/T | 1.706e-05 | 0.00292057 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045639 | CTTTGTAAGCTCATT[C/T]TTGGGGTCCTGTGGC | 672 |
rs777976393 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43053883 | CTGAGGCAGGAGAAT[C/T]ACTTGAACCCTGGAG | 672 |
rs778010977 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118086 | GGGGTGAGATGTACA[-/T]GGGGGGAGTCAGGAA | 672 |
rs778054111 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059678 | AATTTCTCTTTACCT[C/T]ATCCTCCAAATTTAA | 672 |
rs778065395 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43067538 | CGATTACAGGCATGC[A/G]CCACCGTGCCTCGCC | 672 |
rs778076475 | snp | A/G | | | downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43043815 | TGAGCCCTTAGAAAC[A/G]GAGAAATGTCTCTGG | 672 |
rs778115859 | snp | C/T | 0.000132712 | 0.00814483 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067585 | AGCAGATGCAAGGTA[C/T]TCTGTAAAGGTTCTT | 672 |
rs778118145 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092691 | AACCTAGAGCCTCCT[C/T]TGATACTACATTTGG | 672 |
rs778150461 | in-del | -/T | 4.94662e-05 | 0.00497299 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104847 | ACTTGAGTGTCATTC[-/T]TTGGGATATTCAACA | 672 |
rs778170849 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081633 | GCATCTCCTATGTGT[C/G]TGTTTGTTTGCCCCT | 672 |
rs778215185 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093482 | TGTCTGTTCATTTGG[C/T]TTGTTACTCTTCTTG | 672 |
rs778281470 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082937 | GTTAACATTTTATTT[A/G]TATGGGCACATTTCA | 672 |
rs778297428 | in-del | -/TGGA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083910 | TCTGTTGCCCCAGGC[-/TGGA]TGGAGTGCAGTGGTG | 672 |
rs778319854 | snp | A/G | 2.2154e-05 | 0.00332814 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090954 | TTTACCTGAGTGGTT[A/G]AAATGTCACTCTGAG | 672 |
rs778359104 | snp | A/G | 1.65255e-05 | 0.00287445 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094721 | GCCACATGGCTCCAC[A/G]TGCAAGTTTGAAACA | 672 |
rs778364181 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066354 | CTGAAAAACTCTCAA[C/G]AATACTCAAACTAGG | 672 |
rs778371678 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097903 | TAAGGGGGGAAAACA[A/G]TAAGTGTTATGATAA | 672 |
rs778400582 | snp | A/G | | | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43123963 | CAATTCTGTTCATTT[A/G]CATAGGAGATAATCA | 672 |
rs778400777 | snp | C/T | 1.65282e-05 | 0.00287469 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074500 | CCTATCATCTAATGA[C/T]GGGCATTTAGAAGGG | 672 |
rs778487856 | snp | A/G | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070965 | GACACCACCATGGAC[A/G]TTCTTTTGTTGACCC | 672 |
rs778501245 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048673 | GCATGCTCCACCAGG[-/C]CTGGCTACTTTTTGT | 672 |
rs778537466 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43062816 | TGCCCAGGCTGATCT[C/T]GAACTCCTGAGCTCA | 672 |
rs778543267 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116360 | CCACCCCTACCCCAG[A/G]TTATTTTAATTATTA | 672 |
rs778572131 | snp | A/G | 1.65605e-05 | 0.0028775 | intron-variant | BRCA1 | GRCh38.p7 | 17:43082607 | TGGCACCAAGAAAAT[A/G]AAATACTTTGAGAAG | 672 |
rs778607600 | snp | C/G | 1.64803e-05 | 0.00287052 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092306 | CAATTTTGGCCCTCT[C/G]TTTCTACCTAGTTCT | 672 |
rs778648450 | snp | C/T | 7.44962e-05 | 0.00610267 | intron-variant, upstream-variant-2KB | BRCA1, NBR2 | GRCh38.p7 | 17:43125162 | CTCAGGTTCCGCCCC[C/T]ACCCCCCGTCAAAGA | 672 |
rs778655093 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091793 | ACACTCGGTAGCAAC[A/G]GTGCTATGCCTAGTA | 672 |
rs778659819 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100819 | ACACTGCAACCTCCA[C/T]CTCCCTGGTTCAGTT | 672 |
rs778660392 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048017 | GGGCTCAACTTCACC[C/T]CCGGGATTATAGGCA | 672 |
rs778668550 | snp | C/T | 4.94564e-05 | 0.0049725 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094182 | TTACTCTCTACTGAT[C/T]TGGAGTGAACTCTTT | 672 |
rs778668665 | snp | A/T | 3.31697e-05 | 0.00407231 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104266 | GCTGTTTGCATCTGT[A/T]AAATACAAGGGAAAA | 672 |
rs778707598 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076569 | GAAAGGCCTTCTGGA[C/T]TCTGGCTTATAGGGT | 672 |
rs778722177 | in-del | -/TTTC | | | | | GRCh38.p7 | 17:43083166 | CTTTAGTTTCTTTTC[-/TTTC]TTTCTTTCTTTCTTT | 672 |
rs778735627 | snp | C/T | 2.0626e-05 | 0.00321132 | | | GRCh38.p7 | 17:43095966 | GAAACACTAGTTACA[C/T]GTATGCAGAACTGTC | 672 |
rs778744541 | snp | C/T | | | | | GRCh38.p7 | 17:43107962 | ATAAAGGACATAATA[C/T]ACTGGTGAAGGGGGT | 672 |
rs778775133 | snp | A/C/T | 1.66983e-05 | 0.00288944 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124093 | GAAGAGCAGATAAAT[A/C/T]CATTTCTTTCTGTTC | 672 |
rs778810956 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43091129 | CAGGACTGGATTTAC[C/T]TTCATGTCACACAAA | 672 |
rs778824446 | in-del | -/CC | 0.000237727 | 0.0108999 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044827 | TTTTTTTTTTTTGAG[-/CC]ACAGTCTCACTGTCA | 672 |
rs778837077 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066251 | TAAAACCTTAAAAGA[A/G]AAAGGTATAGGACAA | 672 |
rs778868118 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090358 | TCATGTTTTTGCTAT[-/A]GGGGAAATGATGTGT | 672 |
rs778933487 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074617 | AAATGAAACAGCTCA[C/T]GTCAGAGAGATCAGA | 672 |
rs778962676 | snp | A/G | 3.34303e-05 | 0.00408828 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049105 | CTCCCTCTCTGACAG[A/G]GCACCCAATACTTAC | 672 |
rs778965641 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051939 | TGCGCCCGGCCCTCT[C/T]TGACTTTCTTCTAGC | 672 |
rs778988967 | snp | A/G | 1.93902e-05 | 0.00311363 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045618 | TCCCAGGGCCTGGAA[A/G]GGCCACTTTGTAAGC | 672 |
rs778992032 | snp | A/G | 3.32298e-05 | 0.004076 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067579 | TTATGCAGCAGATGC[A/G]AGGTATTCTGTAAAG | 672 |
rs779022501 | in-del | -/AAAG | 5.23729e-05 | 0.005117 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063840 | CAATTCTGAGGTGTT[-/AAAG]GGAGGAGGGGAGAAA | 672 |
rs779046757 | snp | C/G | 1.64738e-05 | 0.00286995 | intron-variant | BRCA1 | GRCh38.p7 | 17:43047621 | GGACCCCATATAGCA[C/G]AGGTACATGCAGGCA | 672 |
rs779097495 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43102798 | GCTGGGACTACAGGC[A/C]CACACCACCATGCCC | 672 |
rs779136512 | in-del | -/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063210 | ATTCTTGATGATCCT[-/C]ATTATCATGGAAAAT | 672 |
rs779137392 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120959 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAGGAG | 672 |
rs779149878 | snp | C/T | 1.85941e-05 | 0.00304905 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079297 | TCTTTCAGTAATTTG[C/T]CAAAATGACGAACAC | 672 |
rs779153035 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092655 | CCAGTTTCGTTGCCT[C/T]TGAACTGAGATGATA | 672 |
rs779168801 | in-del | -/ATGGGTTT | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044443 | AAACAGTCCTGGATA[-/ATGGGTTT]ATGGGTTTATGAAAA | 672 |
rs779192139 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072321 | TCGAACCCAGGAGGC[A/G]GAGGTTGCGCTGAGC | 672 |
rs779201590 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111596 | GGAGGCCAAGGCGGG[C/T]AGATCACGAGGTCAG | 672 |
rs779205984 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43081495 | GGACTGTGGAACGGG[A/G]TGCTGAAGAAGGAAC | 672 |
rs779225364 | snp | C/T | 1.65184e-05 | 0.00287384 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094712 | AGTATTTGTGCCACA[C/T]GGCTCCACATGCAAG | 672 |
rs779225529 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058559 | GCAGAACTTAACAAT[A/C]GGCTTTTCACCTCAC | 672 |
rs779227326 | snp | A/C | 4.94849e-05 | 0.00497393 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093377 | ATTGACAAATTCTTT[A/C]AGTTCACTGGTATTT | 672 |
rs779253414 | snp | A/G | 1.65187e-05 | 0.00287386 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093743 | GTGGATATTTAATTC[A/G]AGTTCCATATTGCTT | 672 |
rs779398652 | in-del | -/AA | 0.311725 | 0.24226 | intron-variant | BRCA1 | GRCh38.p7 | 17:43110588 | GTAAGACCCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 672 |
rs779459487 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092287 | CTAATCTAAGCATAG[C/T]ATTCAATTTTGGCCC | 672 |
rs779477237 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113323 | TTCTAACACAACTCC[C/T]ATACACATATGCAAA | 672 |
rs779507799 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091481 | ATTATTTTCTTCCAA[A/G]CCCGTTCCTCTTTCT | 672 |
rs779557433 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085679 | TGAATGTCTCCTTAA[A/G]TCCCCACCAGGAGGA | 672 |
rs779599663 | snp | C/T | 1.70136e-05 | 0.00291659 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091385 | AGCATAAACATTTAG[C/T]TCACTTCTATAAATA | 672 |
rs779661496 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118506 | CTCAGCCTCCCGAGT[A/C]GCTGGGACTAAAGGC | 672 |
rs779688885 | in-del | -/A | 1.74017e-05 | 0.00294967 | intron-variant | BRCA1 | GRCh38.p7 | 17:43063988 | AAGGATTAGAAGTTG[-/A]AAACAAAATCAGGAA | 672 |
rs779704727 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099845 | AGTTCTCACAGTTCC[A/G]AGGTTAGAGAGTTGG | 672 |
rs779714034 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43114543 | TATAATTCTAGGAAA[C/T]TCATAAAGACTATTC | 672 |
rs779721268 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | BRCA1 | GRCh38.p7 | 17:43057038 | TTTTGTCAACTTGAG[A/G]GAGGGAGCTTTACCT | 672 |
rs779748579 | snp | C/T | 1.64825e-05 | 0.00287071 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093465 | CTGTCATGTCTTTTA[C/T]TTGTCTGTTCATTTG | 672 |
rs779816514 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43061217 | CTATAAGATGCATTC[C/T]CTTCATTTTTCAAGG | 672 |
rs779860754 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43106185 | ATTAACAGACAATGG[C/G]GGCACGGCGATACAG | 672 |
rs779895958 | snp | A/G | 1.64863e-05 | 0.00287104 | BRCA1 | 17 | allele_origin=G(germline)/A(germline) | 17:43092962 | TGAATGTATTCTGCA[A/G]ATACTGAGCATCAAG | 672 |
rs779925378 | in-del | -/AT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059606 | TGCCTTCTTCATCTA[-/AT]TTAATATTACTAACA | 672 |
rs779935143 | snp | A/T | 1.7067e-05 | 0.00292117 | intron-variant | BRCA1 | GRCh38.p7 | 17:43049075 | AGTCTTGCTCACAGG[A/T]GAGAATATTGTGTCC | 672 |
rs779944976 | in-del | -/TTGA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074168 | ATTTTCAAGTAAACC[-/TTGA]TTAACACTTGAGCTA | 672 |
rs779956772 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110094 | AGAGGCGGGGTTTCA[C/T]CATGTTAGCCAGGAT | 672 |
rs779960384 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066004 | ATTTGTCAGTGACCA[C/T]GTTAAAAACCAAGCA | 672 |
rs779974365 | snp | C/T | 1.64991e-05 | 0.00287215 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094303 | CGTCCAATACATCAG[C/T]TACTTTGGCATTTGA | 672 |
rs779995864 | in-del | -/AAAA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43121683 | GCCAAAGTCTGTCTC[-/AAAA]AAAAAAAAAAAAAAA | 672 |
rs780019315 | snp | A/T | 1.64923e-05 | 0.00287156 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045852 | AATTCATTCTCCTGG[A/T]CTAGGCTCTAATCAA | 672 |
rs780108116 | snp | C/G | 1.65198e-05 | 0.00287395 | intron-variant | BRCA1 | GRCh38.p7 | 17:43076664 | TGCTTTGTTCTGATA[C/G]TGATAATTCAGGTTA | 672 |
rs780157871 | snp | C/T | 1.66441e-05 | 0.00288474 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124088 | AACGCGAAGAGCAGA[C/T]AAATCCATTTCTTTC | 672 |
rs780170986 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089653 | CCTGGGTTCAAGTGA[C/T]TCTCCTGCTTTAGCC | 672 |
rs780182824 | in-del | -/TTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064828 | TAGATTTGATTTGCA[-/TTT]TTTTTTTTTTTTTTT | 672 |
rs780228876 | snp | C/T | 0.000185787 | 0.00963634 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044721 | ACCGGTTCTTGAAAA[C/T]CTTCTGCTGTTTTAG | 672 |
rs780239567 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076556 | AAACTTGTCAGCAGA[A/G]AGGCCTTCTGGATTC | 672 |
rs780240240 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43072622 | CAGGCTAGAGTGCAA[C/T]GGCGCGATCTCAGCT | 672 |
rs780261463 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43055369 | TTTAGAATTGGAGGC[C/T]GGGTGCAGTGGCTCA | 672 |
rs780312395 | snp | C/T | 3.38083e-05 | 0.00411133 | intron-variant | BRCA1 | GRCh38.p7 | 17:43091340 | GTTCCTTTAACTATA[C/T]TTGGAAATTTGTAAA | 672 |
rs780367532 | snp | C/T | 1.64879e-05 | 0.00287118 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092646 | GTAATGAGTCCAGTT[C/T]CGTTGCCTCTGAACT | 672 |
rs780412580 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063665 | AGCAGATTAGGTCCT[A/G]TTAGTTATAAAAGAG | 672 |
rs780466817 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069654 | ATGAGATGAAAACAT[C/T]TATAGCCATCACTGT | 672 |
rs780485347 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104920 | TTTCAATAGCTCTTC[A/G]ACAAGTTGACTAAAT | 672 |
rs780620052 | snp | C/T | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43126165 | GCAGGGGAAATGCGC[C/T]CTGGCCCATGTCTGC | 672 |
rs780700729 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43059617 | TCTAATTTAATATTA[A/C]TAACAAGATCTATTG | 672 |
rs780737222 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43110037 | GTAGCTGGGACTACA[C/G]GTGCCCGCTACCACG | 672 |
rs780795747 | snp | A/G | 3.32044e-05 | 0.00407444 | intron-variant | BRCA1 | GRCh38.p7 | 17:43051031 | AAGACAAAGGCTGGT[A/G]CTGGAACTCTGGGGT | 672 |
rs780848687 | snp | A/G | | | upstream-variant-2KB, intron-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43127401 | GGTGGGCACTTGGAG[A/G]ACTTCTGTGTCTAGC | 672 |
rs780850718 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43111808 | GCCTGGGCGACAGAG[C/G]GAGACTCCGTCTCAA | 672 |
rs780869838 | snp | A/T | 1.64882e-05 | 0.00287121 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092022 | GCAGAACTTTCCTTA[A/T]TGTCATTTTCAGCAA | 672 |
rs780870669 | snp | C/T | 1.65403e-05 | 0.00287574 | intron-variant | BRCA1 | GRCh38.p7 | 17:43074311 | AAGTGTTTGTTCCAA[C/T]ACAGCAGATGAAATA | 672 |
rs780886296 | snp | G/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43089494 | TTATTTATTTCATAG[G/T]TGACCAAATTATTGG | 672 |
rs780947950 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050326 | AAATGTTCATGGAGA[C/G]GGCTGGGCACAGTGG | 672 |
rs780952576 | snp | A/C | 1.64784e-05 | 0.00287035 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094636 | ATTCAGCCTTTTCTA[A/C]ATTCATTCTGTCTTT | 672 |
rs780970459 | snp | C/T | 1.65405e-05 | 0.00287576 | intron-variant | BRCA1 | GRCh38.p7 | 17:43067598 | TATTCTGTAAAGGTT[C/T]TTGGTATACCTGTTT | 672 |
rs780985421 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43117710 | CGCCACTGTACTCCA[A/C]CCTGGGCGACAGAGC | 672 |
rs781028704 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43063117 | CTGGTCTTGAACTCC[C/T]GACATCAGGTGATCC | 672 |
rs781031039 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079595 | CACATTAAACACTCT[A/G]AGAGCCAAGACAGCT | 672 |
rs781140529 | snp | C/G | 1.65825e-05 | 0.00287941 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104092 | AAAAGAAAAGAAGAA[C/G]AAGAAGAAGAAGAAA | 672 |
rs781172041 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075249 | ATGTCGACATCTCTA[A/C]ACTCATTCTTTCTAC | 672 |
rs781189797 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43109597 | AGGCTGTCAAAAAGC[C/T]ACCTCCACTGTACAT | 672 |
rs781212379 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091659 | AACAAGCTAGCAGAA[C/T]ATTTTGTTTCCTCAC | 672 |
rs781256590 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104410 | TTTTTAAAAATCAAA[C/T]TTTAAAAAATCAACT | 672 |
rs781260818 | snp | A/G | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082446 | TTCGCAGGTCCTCAA[A/G]GGCAGAAGAGTCACT | 672 |
rs781271325 | snp | C/G | 1.64914e-05 | 0.00287149 | intron-variant | BRCA1 | GRCh38.p7 | 17:43045847 | GTGTCAATTCATTCT[C/G]CTGGACTAGGCTCTA | 672 |
rs781317624 | snp | A/G | 1.8066e-05 | 0.00300544 | intron-variant | BRCA1 | GRCh38.p7 | 17:43079443 | AAGGGAACGGGTACT[A/G]TTCAAAAAGGAATGC | 672 |
rs781319410 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092150 | GTTATCTGAAATCAG[A/G]TATGGAGAGAAATCT | 672 |
rs781321813 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045168 | ATGTTCCACTCCAAC[A/G]TTTGAGAACTGCCCA | 672 |
rs781393191 | snp | A/C | 3.12027e-05 | 0.00394973 | intron-variant | BRCA1 | GRCh38.p7 | 17:43094872 | GCAGCTGAAAATATA[A/C]AAAAATAACAAGGTA | 672 |
rs781404807 | snp | C/T | 3.34348e-05 | 0.00408855 | intron-variant | BRCA1 | GRCh38.p7 | 17:43104284 | ATACAAGGGAAAACA[C/T]TATGTTTGCAGTTAG | 672 |
rs781427381 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43046612 | TCGCCATATTGGCCA[C/G]GCTGGTCTCAAACTC | 672 |
rs781435355 | snp | C/T | 1.64827e-05 | 0.00287073 | BRCA1 | 17 | allele_origin=T(germline)/C(germline) | 17:43092471 | TGTGCTCACTGTACT[C/T]GGAATGTTCTCATTT | 672 |
rs781436492 | in-del | -/ATTA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43078627 | GAAACAAAAGATTGT[-/ATTA]ATTAAACTGTTTTTT | 672 |
rs781440048 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048120 | AGGCTGGTCTTCAGC[A/T]CCCAGGCTCAAGCGA | 672 |
rs781449855 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43083649 | CCTAGAGATCATTAG[C/T]AAGGACCTGTGAGAG | 672 |
rs781476731 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43054867 | CTAGCCTCAGCCTCC[C/T]GAGTAATCCTGAGCT | 672 |
rs781491535 | in-del | -/TT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064829 | AGATTTGATTTGCAT[-/TT]TTTTTTTTTTTTTTT | 672 |
rs781492293 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098003 | ATCCAATTTGAGAGC[C/G]CAGTTTGAATTCTGA | 672 |
rs781493445 | in-del | -/CT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052824 | ACACACACACACACA[-/CT]CTCTTACTTTACCGC | 672 |
rs781513700 | snp | G/T | 4.28201e-05 | 0.0046269 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115805 | AGGGGGGGAGAAAAA[G/T]AAAATAAATGAGGCT | 672 |
rs781525069 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43050209 | TGAAAAGAACAAACC[-/A]AATTTATACACACAC | 672 |
rs781561618 | snp | A/C | 0.000292184 | 0.0120833 | intron-variant | BRCA1 | GRCh38.p7 | 17:43090904 | CTGAATGCAAAGGAC[A/C]CCACACACACGCATG | 672 |
rs781568696 | snp | C/T | 1.88624e-05 | 0.00307097 | intron-variant | BRCA1 | GRCh38.p7 | 17:43115703 | AAGCTAATAATGGAG[C/T]CACATAACACATTCA | 672 |
rs781576075 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100315 | AGCTGATACTTGATA[C/T]ACATTCCAATCACAT | 672 |
rs781635052 | snp | A/C | 0.000186864 | 0.0096642 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | BRCA1 | GRCh38.p7 | 17:43045317 | CTATTCTCTTGAGGC[A/C]AAGCCACTCTGTGCT | 672 |
rs781673566 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069362 | ACACTTCACCAAGTC[C/T]GAATAGAGCTCAAAG | 672 |
rs781708247 | snp | C/T | 0.000167856 | 0.00915967 | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044462 | GGTTTATGAAAAACA[C/T]TTTTTCTTCCTTCAG | 672 |
rs781716310 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048519 | TTTTCTCTCTCTCTC[-/T]TTTTTTTTTTTTTTA | 672 |
rs781732840 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085453 | AGTCATTACTGCCAT[C/T]AGGATAAAATTCCTC | 672 |
rs781746476 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076533 | GTAGAACTATCTGCA[A/G]ACACCTCAAACTTGT | 672 |
rs786201104 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092756 | ACAGACAGTTAATAT[C/T]ACTGCAGGCTTTCCT | 672 |
rs786201160 | snp | A/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094256 | TGAATATTCTGGTTC[A/T]TCAGAGAAAATAGAC | 672 |
rs786201203 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104952 | TTTAATTTCAGGAGC[C/T]TACAAGAAAGTACGA | 672 |
rs786201216 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071000 | CAGGGAGAAGCCAGA[A/G]TTGACAGCTTCAACA | 672 |
rs786201222 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092096 | TCATGCATCTCAGGT[C/T]TGTTCTGAGACACCT | 672 |
rs786201224 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082552 | TACCATGCAACATAA[C/T]CTGATAAAGCTCCAG | 672 |
rs786201232 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093803 | AGAATCACTCGAAAA[A/G]GAATCTGCTTTCAAA | 672 |
rs786201248 | snp | G/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045756 | GACCCGAGAGTGGGT[G/T]TTGGACAGTGTAGCA | 672 |
rs786201256 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104185 | AGTTTCTATCATCCA[A/G]AGTATGGGCTACAGA | 672 |
rs786201258 | snp | A/C | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092456 | AAGTACAGTGAGCAC[A/C]ATTAGCCGTAATAAC | 672 |
rs786201323 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094130 | GAAAACCTATCGGAA[A/G]AAGGCAAGCCTCCCC | 672 |
rs786201338 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094775 | CACCACTGAGAAGCG[C/T]GCAGCTGAGAGGCAT | 672 |
rs786201415 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093059 | CAAAGATAATAGAAA[C/T]GACACAGAAGGCTTT | 672 |
rs786201422 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071162 | TTCTGAAGACAGAGC[C/T]CCAGAGTCAGCTCGT | 672 |
rs786201429 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093656 | TCATGCGCTTGAACT[A/G]GTAGTCAGTAGAAAT | 672 |
rs786201460 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093668 | TACCAGGCATATTCA[C/T]GCGCTTGAACTAGTA | 672 |
rs786201475 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091460 | AGAAAATAATCAAGA[A/G]GAGCAAAGCATGGAT | 672 |
rs786201502 | snp | C/G | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045720 | CCAGTGCCAGGAGCT[C/G]GACACCTACCTGATA | 672 |
rs786201512 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095913 | CTATAGTGTGGGAGA[C/T]CAAGAATTGTTACAA | 672 |
rs786201517 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094316 | TGGGGAGTCTGAATC[A/G]AATGCCAAAGTAGCT | 672 |
rs786201548 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093698 | TAAAAAGAATAGGCT[A/G]AGGAGGAAGTCTTCT | 672 |
rs786201566 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091439 | AAGCATGGATTCAAA[C/T]TTAGGTATTGGAACC | 672 |
rs786201581 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091843 | TGCTTCCAACACTTG[C/T]TATTTGGTAAAGTAA | 672 |
rs786201582 | snp | A/G | | | synonymous-codon, missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047680 | CCCAATTGTGGTTGT[A/G]CAGCCAGATGCCTGG | 672 |
rs786201587 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092522 | GCTAGAGGAAAACTT[C/T]GAGGAACATTCAATG | 672 |
rs786201618 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082534 | GATAAAGCTCCAGCA[A/G]GAAATGGCTGAACTA | 672 |
rs786201623 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091847 | TCCCTGCTTCCAACA[C/T]TTGTTATTTGGTAAA | 672 |
rs786201624 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094556 | ATGGGCTGGAAGTAA[A/G]GAAACATGTAATGAT | 672 |
rs786201634 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094534 | TGTAATGATAGGCGG[A/G]CTCCCAGCACAGAAA | 672 |
rs786201646 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091513 | CTGAGTGACAAGGAA[C/T]TGGTTTCAGATGATG | 672 |
rs786201648 | snp | A/G | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045708 | GCTGGACACCTACCT[A/G]ATACCCCAGATCCCC | 672 |
rs786201649 | snp | G/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093410 | AACAAATGCACCTGG[G/T]TCTTTTACTAAGTGT | 672 |
rs786201658 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074412 | GAGCTCATTAAGGTT[A/G]TTGATGTGGAGGAGC | 672 |
rs786201677 | snp | G/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092861 | CTCTGCCCACTCTGG[G/T]TCCTTAAAGAAACAA | 672 |
rs786201784 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092519 | AGAGGAAAACTTTGA[A/G]GAACATTCAATGTCA | 672 |
rs786201835 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076606 | TTTAAAGCAGTATTA[A/G]CTTCACAGAAAAGTA | 672 |
rs786201839 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071204 | ATCTGGAATCAGCCT[C/T]TTCTCTGATGACCCT | 672 |
rs786201893 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091715 | AAATGACTGCAGTAA[A/C]CAGGTAATATTGGCA | 672 |
rs786201928 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094489 | AATGCTGATCCCCTG[C/T]GTGAGAGAAAAGAAT | 672 |
rs786201944 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093618 | CACCTAATTGTACTG[A/C]ATTGCAAATTGATAG | 672 |
rs786201945 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049131 | AGCTTTCATCATTCA[C/T]CCTTGGCACAGTAAG | 672 |
rs786201948 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094277 | GGACGTTCTAAATGA[A/G]GTAGATGAATATTCT | 672 |
rs786202015 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093397 | GGTTCTTTTACTAAG[C/T]GTTCAAATACCAGTG | 672 |
rs786202022 | snp | A/C | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070985 | ATTGACAGCTTCAAC[A/C]GAAAGGGTCAACAAA | 672 |
rs786202026 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071050 | GCTCATACTACTGAT[A/G]CTGCTGGGTATAATG | 672 |
rs786202040 | in-del | -/GACAG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057056 | GCAAGAGAATCCCAG[-/GACAG]AAAGGTAAAGCTCCC | 672 |
rs786202054 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093091 | GAAAACCCCAAGGGA[C/T]TAATTCATGGTTGTT | 672 |
rs786202058 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43070943 | GGTGGTGTCTGGCCT[A/G]ACCCCAGAAGAATTT | 672 |
rs786202064 | snp | C/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071080 | GTTGCAGAATCTGCC[C/T]AGAGTCCAGCTGCTG | 672 |
rs786202068 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091613 | TGAATTGGAAGACTT[C/G]ACTGCAAATACAAAC | 672 |
rs786202070 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092466 | AGAACATTCCAAGTA[C/T]AGTGAGCACAATTAG | 672 |
rs786202103 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093614 | TAATTGTACTGAATT[A/G]CAAATTGATAGTTGT | 672 |
rs786202106 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090985 | AGCGTCTCTGAAGAC[A/T]GCTCAGGGCTATCCT | 672 |
rs786202155 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092310 | AAGCAGAACTAGGTA[C/G]AAACAGAGGGCCAAA | 672 |
rs786202159 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094460 | ATGGAATAAGCAGAA[A/G]CTGCCATGCTCAGAG | 672 |
rs786202162 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094832 | TTCTGAGACGGATGT[A/G]ACAAATACTGAACAT | 672 |
rs786202165 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074342 | CATCTTACTTGCCAA[A/G]GCAAGATCTAGGTAA | 672 |
rs786202211 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115737 | CACAAAGTGTGACCA[C/T]ATATTTTGCAAGTAA | 672 |
rs786202213 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104147 | CCAAAAGACTTCTAC[A/G]GAGTGAACCCGAAAA | 672 |
rs786202215 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093031 | TTTAAGTATCCATTG[C/G]GACATGAAGTTAACC | 672 |
rs786202249 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092633 | CGAAACTGGACTCAT[C/T]ACTCCAAATAAACAT | 672 |
rs786202263 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094753 | GAGAGGCATCCAGAA[A/C]AGTATCAGGGTAGTT | 672 |
rs786202278 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082492 | AGAACAGCATGGGAG[C/T]CAGCCTTCTAACAGC | 672 |
rs786202286 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43106483 | GGCCTTCACAGTGTC[C/G]TTTATGTAAGAATGA | 672 |
rs786202288 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082442 | ACTCTTCTGCCCTTG[A/G]GGACCTGCGAAATCC | 672 |
rs786202374 | snp | C/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094040 | AATACAAGAGCGTCC[C/G]CTCACAAATAAATTA | 672 |
rs786202378 | in-del | -/TCA | | | cds-indel, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094812 | AAATACTGAACATCA[-/TCA]ACCCAGTAATAATGA | 672 |
rs786202386 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093786 | AATCTGCTTTCAAAA[C/T]GAAAGCTGAACCTAT | 672 |
rs786202387 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43082408 | ACAAAGCACATCAGA[A/G]AAAGGTGTGTATTGT | 672 |
rs786202389 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057091 | CAATGGAAGAAACCA[C/G]CAAGGTCCAAAGCGA | 672 |
rs786202425 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074380 | ACAGCTGGAAGAGTC[C/T]GGGCCACACGATTTG | 672 |
rs786202533 | snp | A/C | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124031 | TATGCAGAAAATCTT[A/C]GAGTGTCCCATCTGG | 672 |
rs786202534 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092521 | CTAGAGGAAAACTTT[C/G]AGGAACATTCAATGT | 672 |
rs786202539 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094305 | AATCAAATGCCAAAG[C/T]AGCTGATGTATTGGA | 672 |
rs786202545 | snp | A/G | | | splice-acceptor-variant | BRCA1 | GRCh38.p7 | 17:43063375 | TTCTATGATCTCTTT[A/G]GGGGTGACCCAGTCT | 672 |
rs786202569 | snp | C/G/T | | | missense, synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091724 | GAATAGCTTAAATGA[C/G/T]TGCAGTAACCAGGTA | 672 |
rs786202573 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071049 | CTCATACTACTGATA[C/G]TGCTGGGTATAATGC | 672 |
rs786202620 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104222 | AAAAGGAAAATAACT[C/G]TCCTGAACATCTAAA | 672 |
rs786202627 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071063 | GAGTCCAGCTGCTGC[C/T]CATACTACTGATACT | 672 |
rs786202631 | snp | A/G | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074483 | CATTAGATGATAGGT[A/G]GTACATGCACAGTTG | 672 |
rs786202635 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074452 | CTCTGGGAGTCTTCA[A/G]AATAGAAACTACCCA | 672 |
rs786202665 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092527 | AATCTGCTAGAGGAA[A/G]ACTTTGAGGAACATT | 672 |
rs786202684 | in-del | -/AAAT | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093130 | AAAACAGAACCAAAT[-/AAAT]GTGTGAGTCAGTGTG | 672 |
rs786202721 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43047691 | CAGGGTGTCCACCCA[A/G]TTGTGGTTGTGCAGC | 672 |
rs786202722 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091949 | TCCTAGCCCTTTCAC[C/T]CATACACATTTGGCT | 672 |
rs786202734 | snp | A/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071023 | AATGCAATGGAAGAA[A/T]GTGTGAGCAGGGAGA | 672 |
rs786202757 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093293 | TAATAATGCTGAAGA[A/C]CCCAAAGATCTCATG | 672 |
rs786202791 | in-del | -/TA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092207 | GTAAGCATCCTGAAA[-/TA]AAAAAGCAAGAATAT | 672 |
rs786202803 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091763 | TCTGTCTAAGAACAC[A/G]GAGGAGAATTTATTA | 672 |
rs786202844 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092018 | TGAAAATGACATTAA[A/G]GAAAGTTCTGCTGTT | 672 |
rs786202898 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092544 | AAACTAAATGTAAGA[A/G]AAATCTGCTAGAGGA | 672 |
rs786202900 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092120 | CTTAGAACAGCCTAT[A/G]GGAAGTAGTCATGCA | 672 |
rs786202906 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092465 | GAACATTCCAAGTAC[-/A]GTGAGCACAATTAGC | 672 |
rs786202919 | in-del | -/AG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093123 | CCAAATAAATGTGTG[-/AG]TCAGTGTGCAGCATT | 672 |
rs786202937 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104247 | GATGCAAACAGCTAT[A/C]ATTTTGCAAAAAAGG | 672 |
rs786202963 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091873 | AACTTATCTAGTGAG[-/G]ATGAAGAGCTTCCCT | 672 |
rs786202998 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091030 | TTTGTTATTTAAGGT[G/T]AAGCAGCATCTGGGT | 672 |
rs786203027 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094686 | ATACTCATGCCAGCT[C/T]ATTACAGCATGAGAA | 672 |
rs786203044 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093756 | TAAGCAGCAGTATAA[A/G]CAATATGGAACTCGA | 672 |
rs786203100 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076592 | AACTTCACAGAAAAG[C/T]AGTGAATACCCTATA | 672 |
rs786203103 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094274 | CGTTCTAAATGAGGT[-/T]AGATGAATATTCTGG | 672 |
rs786203145 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094345 | GAACTGTTAGGTTCT[A/G]ATGACTCACATGATG | 672 |
rs786203149 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076593 | TAACTTCACAGAAAA[-/G]TAGTGAATACCCTAT | 672 |
rs786203152 | snp | C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124086 | AAGAAATGGATTTAT[C/T]TGCTCTTCGCGTTGA | 672 |
rs786203153 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092184 | AAGAATATGAAGAAG[G/T]AGTTCAGACTGTTAA | 672 |
rs786203310 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091887 | AGTCCTCAGAAGAGA[A/G]CTTATCTAGTGAGGA | 672 |
rs786203319 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43115759 | AGTTGATCAAGGAAC[C/T]TGTCTCCACAAAGTG | 672 |
rs786203386 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074432 | GAAACTACCCATCTC[A/G]AGAGGAGCTCATTAA | 672 |
rs786203428 | multinucleotide-polymorphism | AT/TA | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092138 | CATATCTGATTTCAG[AT/TA]AACTTAGAACAGCCT | 672 |
rs786203431 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092159 | TGTTAATACAGATTT[C/T]TCTCCATATCTGATT | 672 |
rs786203432 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104146 | CAAAAGACTTCTACA[-/A]GAGTGAACCCGAAAA | 672 |
rs786203434 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094400 | GATAACACTAAATAG[A/C]AGCATTCAGAAAGTT | 672 |
rs786203435 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093301 | AAAGTGTCTAATAAT[A/G]CTGAAGACCCCAAAG | 672 |
rs786203438 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092050 | GATGGTGAAATAAAG[G/T]AAGATACTAGTTTTG | 672 |
rs786203455 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093565 | AAGAAAAAAAAGTAC[A/G]ACCAAATGCCAGTCA | 672 |
rs786203523 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092995 | CGGGAAACAAGCATA[A/G]AAATGGAAGAAAGTG | 672 |
rs786203524 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076537 | GCTGACAAGTTTGAG[C/G]TGTCTGCAGATAGTT | 672 |
rs786203526 | in-del | -/G | | | splice-donor-variant, intron-variant | BRCA1 | GRCh38.p7 | 17:43106455 | TGATATAACCAAAAG[-/G]TATATAATTTGGTAA | 672 |
rs786203545 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090978 | CTGAAGACTGCTCAG[A/G]GCTATCCTCTCAGAG | 672 |
rs786203547 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063349 | AGTCTATTAAAGAAA[G/T]AAAAATGCTGAATGA | 672 |
rs786203567 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094368 | ATGAGTGGTTTTCCA[C/G]AAGTGATGAACTGTT | 672 |
rs786203578 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094189 | AAAAGTGAAAGAGTT[C/T]ACTCCAAATCAGTAG | 672 |
rs786203580 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091630 | TTTTCTTCACAGTGC[A/G]GTGAATTGGAAGACT | 672 |
rs786203587 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092374 | GGTTCCAGTACTAAT[G/T]AAGTGGGCTCCAGTA | 672 |
rs786203592 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092876 | GGAATGTGCAACATT[-/T]CTCTGCCCACTCTGG | 672 |
rs786203594 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093567 | TAAAGAAAAAAAAGT[-/A]CAACCAAATGCCAGT | 672 |
rs786203663 | multinucleotide-polymorphism | AGTGA/TGTGG | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049164 | TGGATGGTACAGCTG[AGTGA/TGTGG]TGCTTCTGTGGTGAA | 672 |
rs786203671 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094025 | CCTCACAAATAAATT[A/G]AAGCGTAAAAGGAGA | 672 |
rs786203689 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092901 | TTTCAAATCCAGGAA[A/G]TGCAGAAGAGGAATG | 672 |
rs786203694 | in-del | -/AAGGAAGATA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092044 | GATGATGGTGAAATA[-/AAGGAAGATA]CTAGTTTTGCTGAAA | 672 |
rs786203699 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071139 | CAGCTCGTGTTGGCA[A/G]CATACCATCTTCAAC | 672 |
rs786203720 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093605 | TGAATTGCAAATTGA[C/T]AGTTGTTCTAGCAGT | 672 |
rs786203732 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094546 | AGTAAGGAAACATGT[A/T]ATGATAGGCGGACTC | 672 |
rs786203753 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094231 | ATAGACTTACTGGCC[A/G]GTGATCCTCATGAGG | 672 |
rs786203754 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067655 | AACACCACATCACTT[G/T]AACTAATCTAATTAC | 672 |
rs786203786 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092650 | TCTCAGTTCAGAGGC[A/C]ACGAAACTGGACTCA | 672 |
rs786203797 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095876 | CCTCAAGGAACCAGG[A/G]ATGAAATCAGTTTGG | 672 |
rs786203804 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092618 | TACTCCAAATAAACA[C/T]GGACTTTTACAAAAC | 672 |
rs786203823 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091657 | GAGGAAACAAAATGT[C/T]CTGCTAGCTTGTTTT | 672 |
rs786203868 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43067660 | CAGAAAACACCACAT[C/T]ACTTTAACTAATCTA | 672 |
rs786203884 | snp | G/T | | | stop-gained, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091905 | GAGGGGCCAAGAAAT[G/T]AGAGTCCTCAGAAGA | 672 |
rs786203937 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093693 | AGAATAGGCTGAGGA[A/G]GAAGTCTTCTACCAG | 672 |
rs786203939 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104898 | CTATTGAAAATCATT[C/T]GTGCTTTTCAGCTTG | 672 |
rs786203958 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092283 | CAAAATTGAATGCTA[C/T]GCTTAGATTAGGGGT | 672 |
rs786203963 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43051120 | CTTCCTCTCTTCTTC[C/T]AGATCTTCAGGGGGC | 672 |
rs786203965 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093612 | ATTGTACTGAATTGC[A/C]AATTGATAGTTGTTC | 672 |
rs786203979 | snp | A/G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092440 | ATTAGCCGTAATAAC[A/G/T]TTAGAGAAAATGTTT | 672 |
rs786203982 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094054 | ACTGAGCCACAGATA[-/A]TACAAGAGCGTCCCC | 672 |
rs786204049 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093606 | CTGAATTGCAAATTG[A/G]TAGTTGTTCTAGCAG | 672 |
rs786204116 | multinucleotide-polymorphism | AA/TG | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057053 | GAATCCCAGGACAGA[AA/TG]GGTAAAGCTCCCTCC | 672 |
rs786204151 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093106 | CAGTGTGCAGCATTT[A/G]AAAACCCCAAGGGAC | 672 |
rs786204220 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093300 | AAGTGTCTAATAATG[A/C]TGAAGACCCCAAAGA | 672 |
rs786204260 | in-del | -/G | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094290 | TAGCTGATGTATTGG[-/G]ACGTTCTAAATGAGG | 672 |
rs786204261 | in-del | -/CA | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094645 | ATTACTCACTAAAGA[-/CA]GAATGAATGTAGAAA | 672 |
rs786204262 | in-del | -/TAATG | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094543 | AAGTAAGGAAACATG[-/TAATG]ATAGGCGGACTCCCA | 672 |
rs786204263 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093933 | CTCCTGAAATGATAA[A/G]TCAGGGAACTAACCA | 672 |
rs786204264 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093232 | AGATCTGTAGAGAGT[-/T]AGCAGTATTTCATTG | 672 |
rs786204265 | snp | A/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092438 | TAGCCGTAATAACAT[A/T]AGAGAAAATGTTTTT | 672 |
rs786204267 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076585 | CAGAAAAGTAGTGAA[-/A]TACCCTATAAGCCAG | 672 |
rs786204269 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063900 | TTCTAGGAATTGCGG[A/G]AGGAAAATGGGTAGT | 672 |
rs786204270 | in-del | AGG/NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045725 | CACTCTACCAGTGCC[lengthTooLong]AGCTGGACACCTACC | 672 |
rs794726997 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094064 | AGCATTTGTTACTGA[A/G]CCACAGATAATACAA | 672 |
rs794726998 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091673 | GGAACATCACCTTAG[C/T]GAGGAAACAAAATGT | 672 |
rs794727102 | snp | A/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076580 | AAGTAGTGAATACCC[A/T]ATAAGCCAGAATCCA | 672 |
rs794727800 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104124 | CCCGAAAATCCTTCC[C/T]TGGTAAAACCATTTG | 672 |
rs796069013 | in-del | -/CAAGTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43116611 | GCAACCTCTGCCTCC[-/CAAGTT]CAAGTGATTCTCCTG | 672 |
rs796093926 | in-del | -/TA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100559 | ATGTGTGTGTGTGTG[-/TA]TATATATATATAACA | 672 |
rs796218625 | in-del | -/AGC | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43064640 | AGCAGGCTATCTGCA[-/AGC]AGCAGCAGCAGCAGC | 672 |
rs796230530 | in-del | -/AT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100621 | TAACATATATATAAC[-/AT]ATATATATGTTATAT | 672 |
rs796254729 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43098118 | CAGCCTCAAACTCCT[C/G]GGTTCAATGTATCCA | 672 |
rs796257223 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044805 | CTAGTTTCATTTTCC[-/TT]TTTTTTTTTTTTTTT | 672 |
rs796260811 | in-del | -/CA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43052113 | ACACAGATCACACTG[-/CA]CTGCCTCTTCCACTT | 672 |
rs796285317 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43061804 | TGACCAGGCTGGTCT[C/G]GAACTCCTGACCTCA | 672 |
rs796295309 | in-del | CTGACTATCACAAGCTTGAAAC/TTCATCAGTAGGGGTTT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43112722 | CTGACTATCACAATC[lengthTooLong]CAAGCTTCTCACTCT | 672 |
rs796315905 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43084355 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 672 |
rs796336033 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43123330 | AATACCTATCCTCTC[-/A]ACGACACCGATCATC | 672 |
rs796337135 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100627 | ATATATAACATATAT[A/G]TATGTTATATATATA | 672 |
rs796347765 | in-del | -/CCT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095104 | CTATGCAGAAACCAC[-/CCT]ACCTATTTCTCTAAC | 672 |
rs796387434 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100590 | ATATATATAACATAT[A/G]TATATTATATATATA | 672 |
rs796398054 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43057728 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 672 |
rs796452764 | in-del | -/AAAG | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43090058 | AAAAGGGAAAAAAAA[-/AAAG]AAGAAGAGAAAGAAG | 672 |
rs796473027 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43120555 | CGGATCACGAGGTCA[C/G]GAAGTGGAGACCATC | 672 |
rs796503152 | in-del | C/TT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43048520 | TTCTCTCTCTCTCTT[C/TT]TTTTTTTTTTTAGAC | 672 |
rs796566670 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044823 | TTTTTTTTTTTTTTT[-/T]GAGCCACAGTCTCAC | 672 |
rs796612485 | in-del | -/TAT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100610 | TATATATATATAACA[-/TAT]TATATATAACATATA | 672 |
rs796619264 | in-del | -/AT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100575 | ATATATATATATAAC[-/AT]ATATATAACATATAT | 672 |
rs796623638 | in-del | -/ACA | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43070579 | ATTCACCCATGTGAG[-/ACA]ACAAGGGGGAGAAAA | 672 |
rs796628097 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43044822 | TTTTTTTTTTTTTTT[-/TT]GAGCCACAGTCTCAC | 672 |
rs796691137 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43118942 | CTAATTTTTTTGTAT[A/T]TTTGGTAGGGAAGGG | 672 |
rs796697375 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43096590 | AAAAAAAAAAAAAAA[-/A]CCTGGGTCAAGCAAT | 672 |
rs796704325 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066498 | TGACTGCAACCTCAG[C/T]CTCCAGAGTTCAAGC | 672 |
rs796706068 | in-del | A/TT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077745 | TTTTATTTATTTATT[A/TT]TTTTGAGATGGAGTT | 672 |
rs796741862 | in-del | -/CT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43079591 | TGAGCACATTAAACA[-/CT]CTAAGAGCCAAGACA | 672 |
rs796747752 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077751 | TTTATTTATTTTTTT[-/T]GAGATGGAGTTTGCT | 672 |
rs796751222 | snp | A/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43113318 | TCCTTTTCTAACACA[A/T]CTCCTATACACATAT | 672 |
rs796760656 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43119636 | CCAACATTGGTATTA[C/T]TACTGGGACCAAATG | 672 |
rs796766096 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43088073 | ATATATTTTAAAGAT[A/G]AAGTATATACAAGCA | 672 |
rs796773466 | snp | C/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43066961 | TAGCTGGGATTACAG[C/G]TGCCTGCCACCACGC | 672 |
rs796775652 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103238 | CTGGGAGGCCAAGGA[A/G]GGTGGATCACCTGAG | 672 |
rs796783220 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43087596 | GAACCCGGGAGGCAG[A/C]GGATGCGGTGAGCCA | 672 |
rs796797989 | in-del | -/AATGTTCACTGTAACAATGCTTGT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43071520 | AGGTTTAGTCATAGG[-/AATGTTCACTGTAACAATGCTTGT]AATAGTATAATTTTA | 672 |
rs796856605 | in-del | -/CT | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | BRCA1, NBR2 | GRCh38.p7 | 17:43124030 | ACCAGATGGGACACT[-/CT]AAGATTTTCTGCATA | 672 |
rs796876358 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43085675 | TTTGAATGTCTCCTT[-/A]AAGTCCCCACCAGGA | 672 |
rs796877461 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43073645 | TAACTCATAAAAAAA[-/A]CTTGCTTTGGGATTT | 672 |
rs796893963 | in-del | -/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43069290 | AGATCATCTTAATAT[-/G]GGGCTTCAGAATTAA | 672 |
rs796904927 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43103485 | AAAAAAAAAAAAAAA[A/G]AAATCTGTCTTTTTG | 672 |
rs796916234 | in-del | -/TAT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43100647 | TATATATATATAACA[-/TAT]TATATATAACATATA | 672 |
rs796941247 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43058794 | TAAAATATACATTCA[A/G]TGCACTAAAGAAAGT | 672 |
rs796961466 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43122854 | GATCAAGACTATCCT[A/G]GCTAACACGGTGAAA | 672 |
rs796992734 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065092 | GCCTTGGCCCCCCAA[-/A]GCGCTGGGATTACAG | 672 |
rs797019209 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43075760 | ATAGTACTGGACTAC[A/G]TAGTCCAGTACTGGA | 672 |
rs797044631 | in-del | -/CAATATACCTTCTCAGTCTACTAGGCATAGCACCGTTGCTACC | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091783 | AGCACCGTTGCTACC[lengthTooLong]GAGTGTCTGTCTAAG | 672 |
rs797044977 | in-del | -/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43065090 | GTAATCCCAGCGCTT[-/T]GGGGGGCCAAGGCGG | 672 |
rs797044978 | in-del | -/A | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43077744 | TCCATCTCAAAAAAA[-/A]TAAATAAATAAAAAT | 672 |
rs797045175 | in-del | -/TGTG | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43095919 | GTCTTTTCCCTATAG[-/TGTG]GGAGATCAAGAATTG | 672 |
rs863224416 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094514 | CAGCACAGAAAAAAA[A/G]GTAGATCTGAATGCT | 672 |
rs863224417 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115711 | AGTAAGTTTGAATGT[A/G]TTATGTGGCTCCATT | 672 |
rs863224418 | snp | A/G | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104926 | TACGAGATTTAGTCA[A/G]CTTGTTGAAGAGCTA | 672 |
rs863224419 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092108 | TATGGGAAGTAGTCA[C/T]GCATCTCAGGTTTGT | 672 |
rs863224420 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43074531 | TTTCTCCTTCCATTT[A/G]TCTTTCTAGGTCATC | 672 |
rs863224421 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43097236 | TATTGCAGGTGAGTC[A/G]AAGAGAACCTTTGTC | 672 |
rs863224510 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093487 | GGAGCCAAGAAGAGT[-/T]AACAAGCCAAATGAA | 672 |
rs863224511 | snp | G/T | | | stop-gained, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43076498 | AAAAATAAAGAACCA[G/T]GAGTGGAAAGGTAAG | 672 |
rs863224512 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099832 | CTTGGAACTGTGAGA[-/A]CTCTGAGGACAAAGC | 672 |
rs863224752 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094397 | AACACTAAATAGCAG[A/C]ATTCAGAAAGTTAAT | 672 |
rs863224753 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093694 | AAGAATAGGCTGAGG[A/G]GGAAGTCTTCTACCA | 672 |
rs863224754 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092977 | ATGGAAGAAAGTGAA[C/G]TTGATGCTCAGTATT | 672 |
rs863224755 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104895 | TTGAAAATCATTTGT[C/G]CTTTTCAGCTTGACA | 672 |
rs863224756 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092598 | TTTTACAAAACCCAT[A/G]TCGTATACCACCACT | 672 |
rs863224757 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104856 | GAGTGTAAGTGTTGA[A/C]TATCCCAAGAATGAC | 672 |
rs863224758 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092439 | TTAGCCGTAATAACA[G/T]TAGAGAAAATGTTTT | 672 |
rs863224759 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092175 | AAGAAGTAGTTCAGA[C/G]TGTTAATACAGATTT | 672 |
rs863224760 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091824 | TTGGTAAAGTAAACA[A/G]TATACCTTCTCAGTC | 672 |
rs863224761 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074465 | ACATGCACAGTTGCT[C/T]TGGGAGTCTTCAGAA | 672 |
rs863224762 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071221 | GGAACCCCTTACCTG[A/G]AATCTGGAATCAGCC | 672 |
rs863224763 | snp | C/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43063919 | GAACGGACACTGAAA[C/T]ATTTTCTAGGAATTG | 672 |
rs863224764 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057060 | GCAAGAGAATCCCAG[C/G]ACAGAAAGGTAAAGC | 672 |
rs863224765 | snp | C/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43051086 | AAATCTGTTGCTATG[C/G]GCCCTTCACCAACAT | 672 |
rs863224766 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094590 | AACAGCCTGGCTTAG[C/T]AAGGAGCCAACATAA | 672 |
rs863224841 | in-del | -/AAAGAATTT | | | cds-indel, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093368 | AATACCAGTGAACTT[-/AAAGAATTT]GTCAATCCTAGCCTT | 672 |
rs864622080 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091958 | TAGCAGGAGTCCTAG[C/T]CCTTTCACCCATACA | 672 |
rs864622104 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43057104 | GAGGAGATGTGGTCA[A/G]TGGAAGAAACCACCA | 672 |
rs864622119 | in-del | -/GT | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43082398 | ATCAGAAAAAGGTGT[-/GT]ATTGTTGGCCAAACA | 672 |
rs864622122 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092964 | AACTTGATGCTCAGT[A/G]TTTGCAGAATACATT | 672 |
rs864622124 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104181 | TCTATCATCCAAAGT[A/G]TGGGCTACAGAAACC | 672 |
rs864622132 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43071204 | ATCTGGAATCAGCCT[-/T]CTTCTCTGATGACCC | 672 |
rs864622146 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092063 | TGACCTGTTAGATGA[C/T]GGTGAAATAAAGGAA | 672 |
rs864622220 | in-del | -/T | | | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43045745 | GGGTGTTGGACAGTG[-/T]AGCACTCTACCAGTG | 672 |
rs864622233 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43091600 | TTGACTGCAAATACA[A/G]ACACCCAGGATCCTT | 672 |
rs864622244 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43049155 | TGTGTGGTGCTTCTG[C/T]GGTGAAGGAGCTTTC | 672 |
rs864622260 | snp | A/C | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099857 | CAGTCTCAGTGTCCA[A/C]CTCTCTAACCTTGGA | 672 |
rs864622265 | snp | G/T | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43074365 | TGGGCCACACGATTT[G/T]ACGGAAACATCTTAC | 672 |
rs864622306 | snp | C/T | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43095940 | GTTTCTTATTAGGAC[C/T]CTGTCTTTTCCCTAT | 672 |
rs864622350 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43099790 | CCTCAAAAGACGTCT[-/T]GTCTACATTGAATTG | 672 |
rs864622444 | snp | A/G | | | missense, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43104882 | GTGCTTTTCAGCTTG[A/G]CACAGGTTTGGAGTG | 672 |
rs864622452 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093533 | GCACAGCAGAAACCT[A/G]CAACTCATGGAAGGT | 672 |
rs864622454 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094237 | GAGAAAATAGACTTA[C/T]TGGCCAGTGATCCTC | 672 |
rs864622491 | snp | A/C | | | synonymous-codon, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092927 | TTCAAAGCGCCAGTC[A/C]TTTGCTCCGTTTTCA | 672 |
rs864622534 | snp | A/C | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43115797 | TTATTTTCTTTTTCT[A/C]CCCCCCTACCCTGCT | 672 |
rs864622536 | in-del | -/A | | | frameshift-variant, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43093152 | TAGCACTCTAGGGAA[-/A]GGCAAAAACAGAACC | 672 |
rs864622540 | snp | C/T | | | synonymous-codon, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43090947 | TGACATTTTAACCAC[C/T]CAGGTAAAAAGCGTG | 672 |
rs864622588 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092784 | GAAAGAATGAGTCTA[A/T]TATCAAGCCTGTACA | 672 |
rs864622618 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43092690 | CAAATGTAGTATCAA[A/T]GGAGGCTCTAGGTTT | 672 |
rs864622723 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | BRCA1 | GRCh38.p7 | 17:43094396 | ACACTAAATAGCAGC[A/G]TTCAGAAAGTTAATG | 672 |
rs864622737 | snp | A/G | | | intron-variant | BRCA1 | GRCh38.p7 | 17:43104849 | AGTGTTGAATATCCC[A/G]AGAATGACACTCAAG | 672 |