List of variants in gene RAD51C reported as uncertain significance by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.784T>G (p.Leu262Val)	rs149331537	0.00014
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.721G>A (p.Val241Met)	rs184033132	0.00004
NM_058216.3(RAD51C):c.106G>A (p.Glu36Lys)	rs773998134	0.00002
NM_058216.3(RAD51C):c.1109G>A (p.Arg370Gln)	rs373170458	0.00001
NM_058216.3(RAD51C):c.244C>T (p.His82Tyr)	rs1555593593
NM_058216.3(RAD51C):c.395C>G (p.Thr132Arg)	rs730881930
NM_058216.3(RAD51C):c.511G>A (p.Asp171Asn)	rs2143747843
NM_058216.3(RAD51C):c.718A>T (p.Ile240Leu)	rs863224806
NM_058216.3(RAD51C):c.955C>G (p.Arg319Gly)	rs587781287

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.