"Revvity Omics, Revvity"[submitter] AND "RAD51C"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 187716	NM_058216.3(RAD51C):c.181_182del (p.Leu61fs)	RAD51C (L61fs)	Microsatellite (frameshift variant +1 more)	not provided +4 more	GPathogenic
Select item 182844	NM_058216.3(RAD51C):c.224dup (p.Tyr75Ter)	RAD51C (Y75*)	Duplication (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GPathogenic
Select item 418441	NM_058216.3(RAD51C):c.404G>C (p.Cys135Ser)	RAD51C (C135S +1 more)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +3 more	GPathogenic/Likely pathogenic
Select item 6825	NM_058216.3(RAD51C):c.414G>C (p.Leu138Phe)	RAD51C (L138F)	Single nucleotide variant (missense variant)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 128209	NM_058216.3(RAD51C):c.706-2A>G	RAD51C	Single nucleotide variant (splice acceptor variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +5 more	GPathogenic/Likely pathogenic
Select item 186364	NM_058216.3(RAD51C):c.709C>T (p.Arg237Ter)	RAD51C (R237*)	Single nucleotide variant (nonsense +1 more)	Hereditary breast ovarian cancer syndrome +4 more	GPathogenic
Select item 232614	NM_058216.3(RAD51C):c.914G>A (p.Trp305Ter)	RAD51C (W305*)	Single nucleotide variant (nonsense +1 more)	not provided +4 more	GPathogenic/Likely pathogenic

ClinVar