List of variants in gene RAD51C reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
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.922G>T (p.Ala308Ser)	rs185057307	0.00025
NM_058216.3(RAD51C):c.506T>C (p.Val169Ala)	rs587780256	0.00009
NM_058216.3(RAD51C):c.146-3C>T	rs765143155	0.00002
NM_058216.3(RAD51C):c.141C>T (p.Ser47=)	rs568912602	0.00001
NM_058216.3(RAD51C):c.1128A>G (p.Leu376=)	rs545024029
NM_058216.3(RAD51C):c.489T>C (p.Ser163=)	rs876659719
NM_058216.3(RAD51C):c.81G>A (p.Leu27=)	rs1311969744
NM_058216.3(RAD51C):c.87T>C (p.Ser29=)	rs786203249
NM_058216.3(RAD51C):c.886T>C (p.Leu296=)
NM_058216.3(RAD51C):c.966-2169C>G

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.