"Ambry Genetics"[submitter] AND "FGF6"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2374226	NM_020996.3(FGF6):c.590C>A (p.Pro197Gln)	FGF6 (P197Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094752	NM_020996.3(FGF6):c.571C>T (p.Arg191Trp)	FGF6 (R191W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094751	NM_020996.3(FGF6):c.514G>A (p.Glu172Lys)	FGF6 (E172K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094750	NM_020996.3(FGF6):c.448A>C (p.Thr150Pro)	FGF6 (T150P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094749	NM_020996.3(FGF6):c.444C>T (p.Tyr148=)	FGF6	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3278649	NM_020996.3(FGF6):c.418G>T (p.Ala140Ser)	FGF6 (A140S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094748	NM_020996.3(FGF6):c.415G>A (p.Val139Ile)	FGF6 (V139I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2595096	NM_020996.3(FGF6):c.367G>A (p.Val123Met)	FGF6 (V123M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341417	NM_020996.3(FGF6):c.358A>G (p.Ile120Val)	FGF6 (I120V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278646	NM_020996.3(FGF6):c.348C>A (p.Ser116Arg)	FGF6 (S116R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094747	NM_020996.3(FGF6):c.291C>A (p.His97Gln)	FGF6 (H97Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278647	NM_020996.3(FGF6):c.265T>C (p.Tyr89His)	FGF6 (Y89H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094746	NM_020996.3(FGF6):c.190G>A (p.Gly64Arg)	FGF6 (G64R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207271	NM_020996.3(FGF6):c.128G>A (p.Arg43His)	FGF6 (R43H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558892	NM_020996.3(FGF6):c.119C>T (p.Ala40Val)	FGF6 (A40V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance