List of variants in gene RAD51C reported as likely benign for breast-ovarian cancer, familial, susceptibility to, 3

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: 39

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.859A>G (p.Thr287Ala)	rs28363317	0.00653
NM_058216.3(RAD51C):c.572-17G>T	rs193023469	0.00513
NM_058216.3(RAD51C):c.376G>A (p.Ala126Thr)	rs61758784	0.00349
NM_058216.3(RAD51C):c.186A>G (p.Gln62=)	rs28363303	0.00322
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	rs147241704	0.00207
NM_058216.3(RAD51C):c.146-8A>G	rs201079501	0.00074
NM_058216.3(RAD51C):c.706-18T>C	rs56401264	0.00047
NM_058216.3(RAD51C):c.571+16A>G	rs141621051	0.00034
NM_058216.3(RAD51C):c.922G>T (p.Ala308Ser)	rs185057307	0.00025
NM_058216.3(RAD51C):c.890T>C (p.Leu297Pro)	rs143026267	0.00017
NM_058216.3(RAD51C):c.784T>G (p.Leu262Val)	rs149331537	0.00014
NM_058216.3(RAD51C):c.431T>C (p.Ile144Thr)	rs28363307	0.00010
NM_058216.3(RAD51C):c.506T>C (p.Val169Ala)	rs587780256	0.00009
NM_058216.3(RAD51C):c.134A>G (p.Glu45Gly)	rs587781383	0.00006
NM_058216.3(RAD51C):c.14C>T (p.Thr5Met)	rs201523760	0.00006
NM_058216.3(RAD51C):c.336G>A (p.Gly112=)	rs746122031	0.00006
NM_058216.3(RAD51C):c.492T>G (p.Phe164Leu)	rs573992101	0.00006
NM_058216.3(RAD51C):c.1062A>G (p.Ala354=)	rs201000407	0.00004
NM_058216.3(RAD51C):c.546T>G (p.Leu182=)	rs1476282276	0.00004
NM_058216.3(RAD51C):c.706-13C>G	rs747406535	0.00003
NM_058216.3(RAD51C):c.905-19T>C	rs368114768	0.00003
NM_058216.3(RAD51C):c.1089G>A (p.Leu363=)	rs559647198	0.00002
NM_058216.3(RAD51C):c.746G>A (p.Arg249His)	rs730881925	0.00002
NM_058216.3(RAD51C):c.837+14A>G	rs1057517644	0.00002
NM_058216.3(RAD51C):c.141C>T (p.Ser47=)	rs568912602	0.00001
NM_058216.3(RAD51C):c.234A>G (p.Thr78=)	rs730881929	0.00001
NM_058216.3(RAD51C):c.435A>G (p.Pro145=)	rs555235745	0.00001
NM_058216.3(RAD51C):c.537C>T (p.His179=)	rs372385738	0.00001
NM_058216.3(RAD51C):c.79C>T (p.Leu27=)	rs786201775	0.00001
NM_058216.3(RAD51C):c.904+16G>C	rs929872458	0.00001
NM_058216.3(RAD51C):c.905-7C>T	rs757624360	0.00001
NM_058216.3(RAD51C):c.146-15T>C	rs1036386535
NM_058216.3(RAD51C):c.348C>G (p.Pro116=)	rs2047955792
NM_058216.3(RAD51C):c.404+16C>T	rs376465837
NM_058216.3(RAD51C):c.586T>C (p.Leu196=)	rs2143796827
NM_058216.3(RAD51C):c.756A>G (p.Leu252=)	rs863224437
NM_058216.3(RAD51C):c.801G>A (p.Gln267=)	rs2048499866
NM_058216.3(RAD51C):c.838-20C>G	rs766600284
NM_058216.3(RAD51C):c.905-20A>G	rs950351911

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.