"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC129390903"[gen - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 409868	NM_058216.3(RAD51C):c.607A>G (p.Asn203Asp)	LOC129390903, RAD51C (N203D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 409842	NM_058216.3(RAD51C):c.634C>T (p.Arg212Cys)	LOC129390903, RAD51C (R212C)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GUncertain significance
Select item 187633	NM_058216.3(RAD51C):c.635G>A (p.Arg212His)	LOC129390903, RAD51C (R212H)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +5 more	GConflicting classifications of pathogenicity
Select item 186604	NM_058216.3(RAD51C):c.653_654del (p.Glu218fs)	LOC129390903, RAD51C (E218fs)	Microsatellite (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GPathogenic/Likely pathogenic
Select item 962088	NM_058216.3(RAD51C):c.674T>C (p.Leu225Pro)	LOC129390903, RAD51C (L225P)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 232379	NM_058216.3(RAD51C):c.696A>T (p.Glu232Asp)	LOC129390903, RAD51C (E232D)	Single nucleotide variant (missense variant +1 more)	RAD51C-related disorder +4 more	GUncertain significance
Select item 142919	NM_058216.3(RAD51C):c.701C>G (p.Ser234Ter)	LOC129390903, RAD51C (S234*)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GPathogenic
Select item 216807	NM_058216.3(RAD51C):c.705G>T (p.Lys235Asn)	LOC129390903, RAD51C (K235N)	Single nucleotide variant (missense variant +1 more)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 230577	NM_058216.3(RAD51C):c.705+1G>A	LOC129390903, RAD51C	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 378460	NM_058216.3(RAD51C):c.705+14T>C	LOC129390903, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O +3 more	GLikely benign