"Genetic Services Laboratory, University of Chicago"[submitter] AND "Z - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 212628	NM_144969.3(ZDHHC15):c.1008A>G (p.Glu336=)	ZDHHC15	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 199186	NM_144969.3(ZDHHC15):c.747C>T (p.Cys249=)	ZDHHC15	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 1338263	NM_144969.3(ZDHHC15):c.623G>T (p.Arg208Leu)	ZDHHC15 (R199L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 437316	NM_144969.3(ZDHHC15):c.450-4G>A	ZDHHC15	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 1338291	NM_144969.3(ZDHHC15):c.269C>G (p.Ser90Cys)	ZDHHC15 (S81C +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 212631	NM_144969.3(ZDHHC15):c.164-8dup	ZDHHC15	Duplication (intron variant)	not specified	GUncertain significance
Select item 212630	NM_144969.3(ZDHHC15):c.164-8del	ZDHHC15	Deletion (intron variant)	not specified	GBenign
Select item 437317	NM_144969.3(ZDHHC15):c.32G>C (p.Gly11Ala)	ZDHHC15 (G11A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 212629	NM_144969.3(ZDHHC15):c.10G>A (p.Gly4Ser)	ZDHHC15 (G4S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar