List of variants studied for Breast-ovarian cancer, familial, susceptibility to, 4 by MGZ Medical Genetics Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.694C>T (p.Arg232Ter)	rs587780104	0.00004
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys)	rs587781813	0.00004
NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter)	rs387906843	0.00003
NM_002878.4(RAD51D):c.871C>T (p.Arg291Cys)	rs372038369	0.00001
NM_002878.4(RAD51D):c.145-4_145-3delinsTT	rs786202099
NM_002878.4(RAD51D):c.270T>A (p.Asp90Glu)	rs1567728766
NM_002878.4(RAD51D):c.412A>C (p.Asn138His)	rs141690729
NM_002878.4(RAD51D):c.412A>G (p.Asn138Asp)	rs141690729
NM_002878.4(RAD51D):c.480+8C>T
NM_002878.4(RAD51D):c.641C>A (p.Pro214Gln)	rs910355512
NM_002878.4(RAD51D):c.715C>G (p.Arg239Gly)	rs770250516
NM_002878.4(RAD51D):c.791T>C (p.Leu264Pro)	rs1567724947
NM_002878.4(RAD51D):c.901C>T (p.Gln301Ter)	rs1060502959
NM_002878.4(RAD51D):c.916C>T (p.Gln306Ter)

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.