ClinVar Miner

List of variants in gene BRCA2 studied for Ovarian cancer

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.8851G>A (p.Ala2951Thr) rs11571769 0.00809
NM_000059.4(BRCA2):c.440A>G (p.Gln147Arg) rs80358674 0.00025
NM_000059.4(BRCA2):c.5170A>G (p.Ile1724Val) rs35335654 0.00023
NM_000059.4(BRCA2):c.2350A>G (p.Met784Val) rs11571653 0.00018
NM_000059.4(BRCA2):c.1568A>G (p.His523Arg) rs80358443 0.00009
NM_000059.4(BRCA2):c.7006C>T (p.Arg2336Cys) rs431825347 0.00009
NM_000059.4(BRCA2):c.7522G>A (p.Gly2508Ser) rs80358978 0.00004
NM_000059.4(BRCA2):c.8702G>A (p.Gly2901Asp) rs80359129 0.00004
NM_000059.4(BRCA2):c.215A>G (p.Asn72Ser) rs276174818 0.00001
NM_000059.4(BRCA2):c.2186T>C (p.Ile729Thr) rs431825296 0.00001
NM_000059.4(BRCA2):c.2471T>C (p.Leu824Ser) rs397507631 0.00001
NM_000059.4(BRCA2):c.2918C>T (p.Ser973Leu) rs397507296 0.00001
NM_000059.4(BRCA2):c.4376A>G (p.Asn1459Ser) rs117187202 0.00001
NM_000059.4(BRCA2):c.4534C>T (p.Arg1512Cys) rs80358684 0.00001
NM_000059.4(BRCA2):c.5970T>G (p.Asp1990Glu) rs1064794160 0.00001
NM_000059.4(BRCA2):c.7488G>C (p.Lys2496Asn) rs774994294 0.00001
NM_000059.4(BRCA2):c.9538C>T (p.Leu3180Phe) rs200598289 0.00001
NM_000059.4(BRCA2):c.964A>C (p.Lys322Gln) rs11571640 0.00001
NM_000059.4(BRCA2):c.121C>T (p.Pro41Ser) rs80358415
NM_000059.4(BRCA2):c.1732G>C (p.Gly578Arg) rs1555282036
NM_000059.4(BRCA2):c.1871C>T (p.Ala624Val) rs769698255
NM_000059.4(BRCA2):c.2803G>T (p.Asp935Tyr) rs28897716
NM_000059.4(BRCA2):c.3875T>A (p.Leu1292Gln) rs1555283446
NM_000059.4(BRCA2):c.4025G>A (p.Ser1342Asn) rs1270552356
NM_000059.4(BRCA2):c.443G>A (p.Cys148Tyr) rs1204909245
NM_000059.4(BRCA2):c.5682C>G (p.Tyr1894Ter) rs41293497
NM_000059.4(BRCA2):c.572A>T (p.Asp191Val) rs397507798
NM_000059.4(BRCA2):c.5860A>G (p.Thr1954Ala) rs1566233345
NM_000059.4(BRCA2):c.6663C>G (p.Asn2221Lys)
NM_000059.4(BRCA2):c.8354C>T (p.Pro2785Leu) rs786202034
NM_000059.4(BRCA2):c.8948A>T (p.Asp2983Val) rs2137620740
NM_000059.4(BRCA2):c.9053_9057del (p.Ser3018fs) rs869320800
NM_000059.4(BRCA2):c.9545A>C (p.His3182Pro)

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