"Illumina Laboratory Services, Illumina"[submitter] AND "RAD51C"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 324173	NM_058216.3(RAD51C):c.-26C>T	RAD51C	Single nucleotide variant (5 prime UTR variant +1 more)	Breast and Ovarian Cancer Susceptibility +3 more	GBenign/Likely benign
Select item 186825	NM_058216.3(RAD51C):c.87T>C (p.Ser29=)	RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O +4 more	GConflicting classifications of pathogenicity
Select item 140913	NM_058216.3(RAD51C):c.90G>A (p.Ala30=)	RAD51C	Single nucleotide variant (synonymous variant +1 more)	Breast and/or ovarian cancer +5 more	GBenign
Select item 138870	NM_058216.3(RAD51C):c.145+12T>G	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 136156	NM_058216.3(RAD51C):c.146-8A>G	RAD51C	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +6 more	GConflicting classifications of pathogenicity
Select item 138869	NM_058216.3(RAD51C):c.186A>G (p.Gln62=)	RAD51C	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +5 more	GBenign/Likely benign
Select item 136157	NM_058216.3(RAD51C):c.195A>G (p.Arg65=)	RAD51C	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +7 more	GBenign/Likely benign
Select item 492367	NM_058216.3(RAD51C):c.404+7T>C	RAD51C	Single nucleotide variant (3 prime UTR variant +2 more)	Fanconi anemia complementation group O +3 more	GConflicting classifications of pathogenicity
Select item 380341	NM_058216.3(RAD51C):c.404+13G>A	RAD51C	Single nucleotide variant (3 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 492368	NM_058216.3(RAD51C):c.435A>G (p.Pro145=)	RAD51C	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group O +4 more	GConflicting classifications of pathogenicity
Select item 140849	NM_058216.3(RAD51C):c.577C>T (p.Arg193Ter)	RAD51C (R193*)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +5 more	GPathogenic/Likely pathogenic
Select item 496506	NM_058216.3(RAD51C):c.601C>G (p.Leu201Val)	LOC129390903, RAD51C (L201V)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 136162	NM_058216.3(RAD51C):c.721G>A (p.Val241Met)	RAD51C (V241M)	Single nucleotide variant (missense variant +1 more)	Breast and/or ovarian cancer +5 more	GUncertain significance
Select item 128210	NM_058216.3(RAD51C):c.784T>G (p.Leu262Val)	RAD51C (L262V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +7 more	GConflicting classifications of pathogenicity
Select item 128211	NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	RAD51C (G264S)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +8 more	GConflicting classifications of pathogenicity
Select item 889833	NM_058216.3(RAD51C):c.822T>G (p.Asn274Lys)	RAD51C (N274K)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +1 more	GUncertain significance
Select item 132702	NM_058216.3(RAD51C):c.859A>G (p.Thr287Ala)	RAD51C (T287A)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +8 more	GBenign/Likely benign
Select item 128202	NM_058216.3(RAD51C):c.1102C>T (p.Arg368Trp)	RAD51C (R368W)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance
Select item 324174	NM_058216.3(RAD51C):c.*25C>G	RAD51C	Single nucleotide variant (3 prime UTR variant +1 more)	Breast and Ovarian Cancer Susceptibility +3 more	GBenign/Likely benign