List of variants in gene BRCA2 reported as uncertain significance by Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.10095_10096insT (p.Ser3366Ter)	rs730881599	0.00033
NM_000059.4(BRCA2):c.467A>G (p.Asp156Gly)	rs68071147	0.00022
NM_000059.4(BRCA2):c.2320A>G (p.Thr774Ala)	rs55968715	0.00006
NM_000059.4(BRCA2):c.8807T>C (p.Leu2936Ser)	rs398122714	0.00005
NM_000059.4(BRCA2):c.136C>T (p.Pro46Ser)	rs80358425	0.00004
NM_000059.4(BRCA2):c.1762A>G (p.Asn588Asp)	rs398122731	0.00004
NM_000059.4(BRCA2):c.8420C>T (p.Ser2807Leu)	rs55763607	0.00004
NM_000059.4(BRCA2):c.1564G>C (p.Gly522Arg)	rs80358442	0.00003
NM_000059.4(BRCA2):c.6293C>T (p.Ser2098Phe)	rs80358867	0.00003
NM_000059.4(BRCA2):c.9253A>C (p.Thr3085Pro)	rs397507423	0.00003
NM_000059.4(BRCA2):c.8386C>T (p.Pro2796Ser)	rs146120136	0.00002
NM_000059.4(BRCA2):c.2491G>A (p.Val831Ile)	rs397507287	0.00001
NM_000059.4(BRCA2):c.2524G>C (p.Val842Leu)	rs587782454	0.00001
NM_000059.4(BRCA2):c.2698A>G (p.Asn900Asp)	rs55736268	0.00001
NM_000059.4(BRCA2):c.4741G>A (p.Glu1581Lys)	rs368952892	0.00001
NM_000059.4(BRCA2):c.6698C>A (p.Ala2233Asp)	rs41293501	0.00001
NM_000059.4(BRCA2):c.7585G>A (p.Gly2529Ser)	rs398122585	0.00001
NM_000059.4(BRCA2):c.8518A>G (p.Ile2840Val)	rs80359103	0.00001
NM_000059.4(BRCA2):c.8866G>C (p.Glu2956Gln)	rs142040996	0.00001
NM_000059.4(BRCA2):c.8867A>C (p.Glu2956Ala)	rs151174152	0.00001
NM_000059.4(BRCA2):c.9509A>G (p.Asp3170Gly)	rs80359224	0.00001
NM_000059.3(BRCA2):c.7435+10G>A	rs81002793
NM_000059.4(BRCA2):c.1765A>G (p.Lys589Glu)	rs587781801
NM_000059.4(BRCA2):c.2307_2312del (p.Ile770_Leu771del)	rs1555282605
NM_000059.4(BRCA2):c.3677A>T (p.Lys1226Ile)	rs80358612
NM_000059.4(BRCA2):c.5530T>G (p.Phe1844Val)
NM_000059.4(BRCA2):c.641AAG[1] (p.Glu215del)	rs80359588
NM_000059.4(BRCA2):c.68-7del	rs276174878
NM_000059.4(BRCA2):c.7772A>G (p.Asn2591Ser)	rs80359006
NM_000059.4(BRCA2):c.8191C>G (p.Gln2731Glu)	rs397507966
NM_000059.4(BRCA2):c.8772G>C (p.Glu2924Asp)	rs863224318
NM_000059.4(BRCA2):c.8825C>T (p.Ala2942Val)	rs373227180
NM_000059.4(BRCA2):c.8844T>G (p.Ile2948Met)	rs1064793691
NM_000059.4(BRCA2):c.9344A>G (p.Lys3115Arg)	rs276174923

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