"Invitae"[submitter] AND "ACP1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 717141	NM_004300.4(ACP1):c.21G>T (p.Lys7Asn)	ACP1 (K7N)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 788388	NM_004300.4(ACP1):c.43+8G>A	ACP1, LOC129932975	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 712259	NM_004300.4(ACP1):c.43+10C>T	ACP1, LOC129932975	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 756151	NM_004300.4(ACP1):c.96C>T (p.Thr32=)	ACP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 712497	NM_004300.4(ACP1):c.402G>A (p.Gly134=)	ACP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 711059	NM_004300.4(ACP1):c.423G>A (p.Thr141=)	ACP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

ClinVar