ClinVar Miner

List of variants in gene RAD51C reported as uncertain significance by Hereditary Cancer Group, L’Institut d'Investigació Biomèdica de Bellvitge

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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.1009G>T (p.Val337Leu) rs2049473367
NM_058216.3(RAD51C):c.13A>T (p.Thr5Ser) rs1314517659
NM_058216.3(RAD51C):c.308T>A (p.Phe103Tyr) rs2143723981
NM_058216.3(RAD51C):c.310T>C (p.Cys104Arg) rs2047952776
NM_058216.3(RAD51C):c.388G>A (p.Gly130Arg) rs773293999
NM_058216.3(RAD51C):c.398A>G (p.Gln133Arg) rs2143727988
NM_058216.3(RAD51C):c.425T>C (p.Val142Ala) rs2143744027
NM_058216.3(RAD51C):c.467T>G (p.Val156Gly) rs1435180142
NM_058216.3(RAD51C):c.472A>T (p.Ile158Phe) rs771888635
NM_058216.3(RAD51C):c.489T>G (p.Ser163Arg) rs876659719
NM_058216.3(RAD51C):c.65C>T (p.Ala22Val) rs2143676047
NM_058216.3(RAD51C):c.752A>G (p.Asp251Gly) rs2048496443
NM_058216.3(RAD51C):c.871G>A (p.Asp291Asn) rs2143930779
NM_058216.3(RAD51C):c.882G>C (p.Gln294His) rs2143931255
NM_058216.3(RAD51C):c.89C>A (p.Ala30Glu) rs1000113630
NM_058216.3(RAD51C):c.947A>G (p.His316Arg) rs2143962686

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