"Ambry Genetics"[submitter] AND "FUT9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2251484	NM_006581.4(FUT9):c.102C>G (p.Asn34Lys)	FUT9, UFL1-AS1 (N34K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097540	NM_006581.4(FUT9):c.131C>A (p.Ala44Asp)	FUT9, UFL1-AS1 (A44D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225814	NM_006581.4(FUT9):c.284C>T (p.Thr95Met)	FUT9, UFL1-AS1 (T95M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471318	NM_006581.4(FUT9):c.341G>A (p.Ser114Asn)	FUT9, UFL1-AS1 (S114N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487603	NM_006581.4(FUT9):c.437G>C (p.Ser146Thr)	FUT9, UFL1-AS1 (S146T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097541	NM_006581.4(FUT9):c.593C>T (p.Pro198Leu)	FUT9, UFL1-AS1 (P198L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312424	NM_006581.4(FUT9):c.983G>A (p.Arg328Gln)	FUT9, UFL1-AS1 (R328Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar