List of variants in gene BARD1 reported as likely benign by Counsyl

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1972C>T (p.Arg658Cys)	rs3738888	0.00736
NM_000465.4(BARD1):c.1977A>G (p.Arg659=)	rs147215925	0.00230
NM_000465.4(BARD1):c.620A>G (p.Lys207Arg)	rs34969857	0.00218
NM_000465.4(BARD1):c.33G>T (p.Gln11His)	rs143914387	0.00176
NM_000465.4(BARD1):c.2282G>A (p.Ser761Asn)	rs142155101	0.00153
NM_000465.4(BARD1):c.57G>A (p.Glu19=)	rs730881406	0.00019
NM_000465.4(BARD1):c.1059C>G (p.Pro353=)	rs368649242	0.00009
NM_000465.4(BARD1):c.722C>G (p.Ser241Cys)	rs3738885	0.00006
NM_000465.4(BARD1):c.1315-21C>A	rs747393586	0.00001
NM_000465.4(BARD1):c.1811-16dup	rs760333316
NM_000465.4(BARD1):c.215+20T>C	rs200715720
NM_000465.4(BARD1):c.2191C>G (p.Arg731Gly)	rs76744638
NM_000465.4(BARD1):c.364+16A>G	rs201219625
NM_000465.4(BARD1):c.365-8del	rs776103948

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.