"Ambry Genetics"[submitter] AND "FGF10"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2368459	NM_004465.2(FGF10):c.553G>A (p.Ala185Thr)	FGF10 (A185T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2542857	NM_004465.2(FGF10):c.453G>C (p.Lys151Asn)	FGF10 (K151N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 7534	NM_004465.2(FGF10):c.240A>C (p.Arg80Ser)	FGF10 (R80S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2549501	NM_004465.2(FGF10):c.155C>A (p.Ser52Tyr)	FGF10 (S52Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3278618	NM_004465.2(FGF10):c.134T>A (p.Val45Glu)	FGF10 (V45E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2246123	NM_004465.2(FGF10):c.133G>C (p.Val45Leu)	FGF10 (V45L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2206311	NM_004465.2(FGF10):c.130A>G (p.Met44Val)	FGF10 (M44V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2171727	NM_004465.2(FGF10):c.64T>C (p.Cys22Arg)	FGF10 (C22R)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance

ClinVar