List of variants in gene BRCA2 reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.6513G>C (p.Val2171=)	rs206076	0.99779
NM_000059.4(BRCA2):c.4563A>G (p.Leu1521=)	rs206075	0.97986
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.3807T>C (p.Val1269=)	rs543304	0.18035
NM_000059.4(BRCA2):c.2971A>G (p.Asn991Asp)	rs1799944	0.04357
NM_000059.4(BRCA2):c.2229T>C (p.His743=)	rs1801499	0.04095
NM_000059.4(BRCA2):c.1365A>G (p.Ser455=)	rs1801439	0.04091
NM_000059.4(BRCA2):c.10234A>G (p.Ile3412Val)	rs1801426	0.03864
NM_000059.4(BRCA2):c.865A>C (p.Asn289His)	rs766173	0.03693
NM_000059.4(BRCA2):c.7397= (p.Val2466=)	rs169547	0.01961
NM_000059.4(BRCA2):c.5744C>T (p.Thr1915Met)	rs4987117	0.01796
NM_000059.4(BRCA2):c.8830A>T (p.Ile2944Phe)	rs4987047	0.01180
NM_000059.4(BRCA2):c.7469T>C (p.Ile2490Thr)	rs11571707	0.00895
NM_000059.4(BRCA2):c.7017G>C (p.Lys2339Asn)	rs45574331	0.00792
NM_000059.4(BRCA2):c.1788T>C (p.Asp596=)	rs11571642	0.00768
NM_000059.4(BRCA2):c.4258G>T (p.Asp1420Tyr)	rs28897727	0.00609
NM_000059.4(BRCA2):c.5704G>A	rs4987048	0.00598
NM_000059.4(BRCA2):c.5199C>T (p.Ser1733=)	rs28897734	0.00488
NM_000059.4(BRCA2):c.2960A>T (p.Asn987Ile)	rs2227944	0.00356
NM_000059.4(BRCA2):c.2786T>C (p.Leu929Ser)	rs2227943	0.00322
NM_000059.4(BRCA2):c.4068G>A (p.Leu1356=)	rs28897724	0.00295
NM_000059.4(BRCA2):c.6323G>A (p.Arg2108His)	rs35029074	0.00247
NM_000059.4(BRCA2):c.8182G>A (p.Val2728Ile)	rs28897749	0.00239
NM_000059.4(BRCA2):c.125A>G (p.Tyr42Cys)	rs4987046	0.00158
NM_000059.4(BRCA2):c.8149G>T (p.Ala2717Ser)	rs28897747	0.00127
NM_000059.4(BRCA2):c.978C>A (p.Ser326Arg)	rs28897706	0.00079
NM_000059.4(BRCA2):c.1786G>C (p.Asp596His)	rs56328701	0.00025
NM_000059.4(BRCA2):c.1385A>G (p.Glu462Gly)	rs56403624	0.00019
NM_000059.4(BRCA2):c.2944A>C (p.Ile982Leu)	rs28897717	0.00003
NM_000059.4(BRCA2):c.7242A>G (p.Ser2414=)	rs1799955

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