ClinVar Miner

List of variants in gene RAD51C reported as benign for not specified

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.904+34T>C rs28363318 0.30375
NM_058216.3(RAD51C):c.-26C>T rs12946397 0.18608
NM_058216.3(RAD51C):c.90G>A (p.Ala30=) rs115414895 0.01193
NM_058216.3(RAD51C):c.405-49C>T rs116809738 0.00838
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.571+16A>G rs141621051 0.00034
NM_058216.3(RAD51C):c.744T>C (p.Phe248=) rs150142859 0.00016
NM_058216.3(RAD51C):c.*25C>G rs28363336 0.00011
NM_058216.2(RAD51C):c.-48G>T rs774649783 0.00006
NM_058216.3(RAD51C):c.1062A>G (p.Ala354=) rs201000407 0.00004
NM_058216.3(RAD51C):c.945T>C (p.Phe315=) rs201235884 0.00002
NM_058216.3(RAD51C):c.948T>C (p.His316=) rs773196250 0.00002
NM_058216.3(RAD51C):c.189T>C (p.Ile63=) rs730881923
NM_058216.3(RAD51C):c.404+13G>A rs547506164

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