List of variants in gene BRCA2 reported by Division of Medical Genetics, University of Washington

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.352C>T (p.Arg118Cys)	rs375125172	0.00004
NM_000059.4(BRCA2):c.3264dup (p.Gln1089fs)	rs80359380	0.00001
NM_000059.4(BRCA2):c.4316C>A (p.Ala1439Asp)	rs80358667	0.00001
NM_000059.4(BRCA2):c.1755_1759del (p.Lys585fs)	rs80359302
NM_000059.4(BRCA2):c.2834_2835del (p.Lys945fs)	rs80359356
NM_000059.4(BRCA2):c.3744_3747del (p.Ser1248fs)	rs80359403
NM_000059.4(BRCA2):c.5575A>G (p.Ile1859Val)	rs397507354
NM_000059.4(BRCA2):c.7874G>A (p.Arg2625Lys)	rs864622552
NM_000059.4(BRCA2):c.7913_7917del (p.Ala2637_Phe2638insTer)	rs80359686
NM_000059.4(BRCA2):c.9304G>T (p.Ala3102Ser)	rs747073940

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.