List of variants reported as likely pathogenic for Breast-ovarian cancer, familial, susceptibility to, 3 by Hereditary Cancer Group, L’Institut d'Investigació Biomèdica de Bellvitge

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

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.404+1G>C	rs1555593939
NM_058216.3(RAD51C):c.572-1G>T	rs1413872299
NM_058216.3(RAD51C):c.705+1G>T	rs876658644
NM_058216.3(RAD51C):c.706-1G>A	rs1555599090
NM_058216.3(RAD51C):c.708_837+2del
NM_058216.3(RAD51C):c.801del (p.Gln267fs)	rs2143853790
NM_058216.3(RAD51C):c.837+5G>T	rs1567799952
NM_058216.3(RAD51C):c.966delG	rs2144044105
NM_058216.3:c.1_571del
NM_058216.3:c.905_966del

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.