List of variants in gene BRCA2 reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.4068G>A (p.Leu1356=)	rs28897724	0.00295
NM_000059.4(BRCA2):c.5198C>T (p.Ser1733Phe)	rs55639415	0.00069
NM_000059.4(BRCA2):c.1395A>C (p.Val465=)	rs11571641	0.00026
NM_000059.4(BRCA2):c.9649-20C>T	rs56177715	0.00016
NM_000059.4(BRCA2):c.3262C>T (p.Pro1088Ser)	rs80358572	0.00009
NM_000059.4(BRCA2):c.5635G>A (p.Glu1879Lys)	rs55996097	0.00008
NM_000059.4(BRCA2):c.831T>G (p.Asn277Lys)	rs28897705	0.00006
NM_000059.4(BRCA2):c.7010C>T (p.Thr2337Ile)	rs80358927	0.00004
NM_000059.4(BRCA2):c.5986G>A (p.Ala1996Thr)	rs80358833	0.00003
NM_000059.4(BRCA2):c.9116C>G (p.Pro3039Arg)	rs80359167	0.00003
NM_000059.4(BRCA2):c.5688A>G (p.Ala1896=)	rs768907899	0.00002
NM_000059.4(BRCA2):c.7507G>A (p.Val2503Ile)	rs587782191	0.00002
NM_000059.4(BRCA2):c.1342C>T (p.Arg448Cys)	rs80358422	0.00001
NM_000059.4(BRCA2):c.1392G>A (p.Val464=)	rs1060504613	0.00001
NM_000059.4(BRCA2):c.1818G>A (p.Pro606=)	rs76844014	0.00001
NM_000059.4(BRCA2):c.2416G>C (p.Asp806His)	rs56404215	0.00001
NM_000059.4(BRCA2):c.2924T>A (p.Ile975Asn)	rs398122756	0.00001
NM_000059.4(BRCA2):c.6458C>T (p.Pro2153Leu)	rs276174873	0.00001
NM_000059.4(BRCA2):c.7232A>C (p.Lys2411Thr)	rs80358950	0.00001
NM_000059.4(BRCA2):c.1675G>A (p.Asp559Asn)	rs1555282012
NM_000059.4(BRCA2):c.1816C>T (p.Pro606Ser)	rs765924757
NM_000059.4(BRCA2):c.1860T>G (p.Phe620Leu)	rs1064793402
NM_000059.4(BRCA2):c.5117A>C (p.Asn1706Thr)	rs730881536
NM_000059.4(BRCA2):c.5213C>T (p.Thr1738Ile)	rs1593904785
NM_000059.4(BRCA2):c.5682C>T (p.Tyr1894=)	rs41293497
NM_000059.4(BRCA2):c.6101G>A (p.Arg2034His)	rs80358849
NM_000059.4(BRCA2):c.6369A>C (p.Glu2123Asp)	rs1064793571
NM_000059.4(BRCA2):c.6757C>G (p.Leu2253Val)	rs1555284846
NM_000059.4(BRCA2):c.7051G>T (p.Ala2351Ser)	rs80358930
NM_000059.4(BRCA2):c.7370T>G (p.Phe2457Cys)	rs876661273
NM_000059.4(BRCA2):c.7731A>C (p.Lys2577Asn)	rs2137567171
NM_000059.4(BRCA2):c.8826T>C (p.Ala2942=)	rs1131692125

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