List of variants reported as likely pathogenic for breast-ovarian cancer, familial, susceptibility to, 4 by Counsyl

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.363del (p.Ala122fs)	rs730881935	0.00002
NM_002878.4(RAD51D):c.451C>T (p.Gln151Ter)	rs587781756	0.00002
NM_002878.4(RAD51D):c.620C>T (p.Ser207Leu)	rs370228071	0.00002
NM_002878.4(RAD51D):c.649G>T (p.Gly217Ter)	rs775365939	0.00001
NM_002878.4(RAD51D):c.655C>T (p.Gln219Ter)	rs771007945	0.00001
NM_002878.4(RAD51D):c.1A>G (p.Met1Val)	rs561425038
NM_002878.4(RAD51D):c.1A>T (p.Met1Leu)	rs561425038
NM_002878.4(RAD51D):c.270_271dup (p.Lys91fs)	rs753862052
NM_002878.4(RAD51D):c.6_13dup (p.Arg5fs)	rs1555570506
NM_002878.4(RAD51D):c.740_741dup (p.Thr248Ter)	rs1555567197
NM_002878.4(RAD51D):c.81del (p.Val28fs)	rs1064793952
NM_002878.4(RAD51D):c.85del (p.Val29fs)	rs1057517586
NM_002878.4(RAD51D):c.94_95del (p.Val32fs)	rs786203137

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.