ClinVar Miner

List of variants in gene RAD51C reported as benign for Fanconi anemia complementation group O

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.904+34T>C rs28363318 0.30375
NM_058216.3(RAD51C):c.90G>A (p.Ala30=) rs115414895 0.01193
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.837+13T>C rs188613030 0.00112
NM_058216.3(RAD51C):c.195A>G (p.Arg65=) rs45511291 0.00105
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.1026+13T>C rs531535812
NM_058216.3(RAD51C):c.1027-10del rs768715761
NM_058216.3(RAD51C):c.1027-10dup rs768715761
NM_058216.3(RAD51C):c.146-9del
NM_058216.3(RAD51C):c.459T>G (p.Gly153=) rs769486350
NM_058216.3(RAD51C):c.572-11del rs587780258

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.