ClinVar Miner

List of variants in gene BRCA2 reported by Genomic Research Center, Shahid Beheshti University of Medical Sciences

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.3396A>G (p.Lys1132=) rs1801406 0.28273
NM_000059.4(BRCA2):c.1114A>C (p.Asn372His) rs144848 0.23116
NM_000059.4(BRCA2):c.-26G>A rs1799943 0.20795
NM_000059.4(BRCA2):c.8117A>G (p.Asn2706Ser) rs80359055 0.00001
NM_000059.4(BRCA2):c.9117G>A (p.Pro3039=) rs28897756 0.00001
NM_000059.4(BRCA2):c.1813dup (p.Ile605fs) rs80359306
NM_000059.4(BRCA2):c.2957dup (p.Asn986fs) rs80359365
NM_000059.4(BRCA2):c.331A>G (p.Asn111Asp) rs1555280839
NM_000059.4(BRCA2):c.3455T>G (p.Leu1152Ter) rs80358593
NM_000059.4(BRCA2):c.3751dup (p.Thr1251fs) rs397507683
NM_000059.4(BRCA2):c.3830del (p.Asn1277fs) rs397507689
NM_000059.4(BRCA2):c.5081G>T (p.Arg1694Ile) rs753721331
NM_000059.4(BRCA2):c.5350_5351del (p.Asn1784fs) rs80359507
NM_000059.4(BRCA2):c.5555T>A (p.Val1852Asp) rs483352930
NM_000059.4(BRCA2):c.6261_6262insGT (p.Thr2088fs) rs1555284614
NM_000059.4(BRCA2):c.6841+80_6841+83del rs11571661
NM_000059.4(BRCA2):c.7679_7680del (p.Phe2560fs) rs80359673
NM_000059.4(BRCA2):c.793+64del rs751977993
NM_000059.4(BRCA2):c.8395del (p.Arg2799fs) rs80359709
NM_000059.4(BRCA2):c.8490G>A (p.Trp2830Ter) rs587776351
NM_000059.4(BRCA2):c.8585dup (p.Glu2863fs) rs80359720
NM_000059.4(BRCA2):c.8677C>T (p.Gln2893Ter) rs397507409
NM_000059.4(BRCA2):c.9076C>T (p.Gln3026Ter) rs80359159
NM_000059.4(BRCA2):c.9266C>T (p.Pro3089Leu) rs1555289499
NM_000059.4(BRCA2):c.9827G>A (p.Arg3276Lys) rs1555289967

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