Related gene-specific medical variations for Gene (Select 51304) - ClinVar - NCBI

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Links from Gene

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 2512318	NM_001135179.2(ZDHHC3):c.83C>G (p.Pro28Arg)	LOC126806665, ZDHHC3 (P28R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
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 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 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 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 98367	NM_001135179.2(ZDHHC3):c.147C>T (p.Ile49=)	LOC126806665, ZDHHC3	Single nucleotide variant (synonymous variant +2 more)	not provided	Gnot provided
Select item 98366	NM_001135179.2(ZDHHC3):c.617G>C (p.Ser206Thr)	ZDHHC3 (S206T +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	Gnot provided