ClinVar Miner

Variants in gene RAD51C with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 23
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HGVS dbSNP gnomAD frequency
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.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_058216.3(RAD51C):c.506T>C (p.Val169Ala) rs587780256 0.00009
NM_058216.3(RAD51C):c.336G>A (p.Gly112=) rs746122031 0.00006
NM_058216.3(RAD51C):c.870T>A (p.Ile290=) rs376402418 0.00006
NM_058216.3(RAD51C):c.1062A>G (p.Ala354=) rs201000407 0.00004
NM_058216.3(RAD51C):c.905-19T>C rs368114768 0.00003
NM_058216.3(RAD51C):c.-13A>G rs759669075 0.00002
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.141C>T (p.Ser47=) rs568912602 0.00001

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