"Ambry Genetics"[submitter] AND "LOC126806665"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2468754	NM_001135179.2(ZDHHC3):c.287G>A (p.Arg96Gln)	LOC126806665, ZDHHC3 (R96Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2238247	NM_001135179.2(ZDHHC3):c.241A>G (p.Ile81Val)	LOC126806665, ZDHHC3 (I81V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192727	NM_001135179.2(ZDHHC3):c.220G>A (p.Val74Met)	LOC126806665, ZDHHC3 (V74M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2353714	NM_001135179.2(ZDHHC3):c.212G>A (p.Arg71Gln)	LOC126806665, ZDHHC3 (R71Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2224353	NM_001135179.2(ZDHHC3):c.136G>A (p.Ala46Thr)	LOC126806665, ZDHHC3 (A46T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 98368	NM_001135179.2(ZDHHC3):c.86A>G (p.Tyr29Cys)	LOC126806665, ZDHHC3 (Y29C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2512318	NM_001135179.2(ZDHHC3):c.83C>G (p.Pro28Arg)	LOC126806665, ZDHHC3 (P28R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

ClinVar