"Genome-Nilou Lab"[submitter] AND "FANCC"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 134299	NM_000136.3(FANCC):c.1414G>A (p.Gly472Arg)	AOPEP, FANCC (G472R)	Single nucleotide variant (missense variant)	Fanconi anemia +4 more	GConflicting classifications of pathogenicity
Select item 255273	NM_000136.3(FANCC):c.1155-38T>C	AOPEP, FANCC	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 134305	NM_000136.3(FANCC):c.584A>T (p.Asp195Val)	AOPEP, FANCC (D195V)	Single nucleotide variant (missense variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 1177025	NM_000136.3(FANCC):c.521+109A>G	FANCC	Single nucleotide variant (intron variant)	Fanconi anemia complementation group C +1 more	GBenign
Select item 409660	NM_000136.3(FANCC):c.509A>G (p.Asn170Ser)	FANCC (N170S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 127537	NM_000136.3(FANCC):c.178G>A (p.Val60Ile)	FANCC (V60I)	Single nucleotide variant (missense variant)	Fanconi anemia +5 more	GConflicting classifications of pathogenicity
Select item 134301	NM_000136.3(FANCC):c.77C>T (p.Ser26Phe)	FANCC (S26F)	Single nucleotide variant (missense variant)	Fanconi anemia +5 more	GConflicting classifications of pathogenicity

ClinVar