"GeneKor MSA"[submitter] AND "RAD51C"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 136160	NM_058216.3(RAD51C):c.523G>A (p.Ala175Thr)	RAD51C (A175T)	Single nucleotide variant (missense variant)	not specified +5 more	GUncertain significance
Select item 241773	NM_058216.3(RAD51C):c.622A>G (p.Ile208Val)	LOC129390903, RAD51C (I208V)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 241775	NM_058216.3(RAD51C):c.705+3A>G	LOC129390903, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 141175	NM_058216.3(RAD51C):c.778C>T (p.Arg260Trp)	RAD51C (R260W)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GUncertain significance
Select item 128211	NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	RAD51C (G264S)	Single nucleotide variant (missense variant +1 more)	RAD51C-related disorder +8 more	GConflicting classifications of pathogenicity
Select item 142762	NM_058216.3(RAD51C):c.904+5G>T	RAD51C	Single nucleotide variant (intron variant)	Breast and/or ovarian cancer +5 more	GPathogenic/Likely pathogenic
Select item 245991	NM_058216.3(RAD51C):c.905-2A>G	RAD51C	Single nucleotide variant (splice acceptor variant)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic/Likely pathogenic
Select item 584558	NM_058216.3(RAD51C):c.912T>G (p.Ser304Arg)	RAD51C (S304R)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +1 more	GUncertain significance