"Ambry Genetics"[submitter] AND "ACP1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2484517	NM_004300.4(ACP1):c.23C>T (p.Ser8Phe)	ACP1 (S8F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491403	NM_004300.4(ACP1):c.116A>T (p.Asn39Ile)	ACP1 (N39I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138662	NM_004300.4(ACP1):c.231+57G>A	ACP1 (G45S)	Single nucleotide variant (synonymous variant +3 more)	not specified	GUncertain significance
Select item 2552586	NM_004300.4(ACP1):c.231+100G>T	ACP1 (E111* +1 more)	Single nucleotide variant (nonsense +3 more)	not specified	GUncertain significance
Select item 2267747	NM_004300.4(ACP1):c.272G>T (p.Cys91Phe)	ACP1 (C91F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138677	NM_004300.4(ACP1):c.428A>G (p.Tyr143Cys)	ACP1 (Y143C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar