Related gene-specific medical variations for Gene (Select 51201) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3192697	NM_016353.5(ZDHHC2):c.92G>C (p.Gly31Ala)	LOC129999929, ZDHHC2 (G31A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192693	NM_016353.5(ZDHHC2):c.16C>T (p.Pro6Ser)	LOC129999929, ZDHHC2 (P6S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658443	NM_016353.5(ZDHHC2):c.85C>T (p.Leu29=)	LOC129999929, ZDHHC2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2534764	NM_016353.5(ZDHHC2):c.29C>T (p.Ala10Val)	LOC129999929, ZDHHC2 (A10V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2524072	NM_016353.5(ZDHHC2):c.80C>G (p.Thr27Ser)	LOC129999929, ZDHHC2 (T27S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2495302	NM_016353.5(ZDHHC2):c.61A>G (p.Ile21Val)	LOC129999929, ZDHHC2 (I21V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468874	NM_016353.5(ZDHHC2):c.67G>T (p.Val23Leu)	LOC129999929, ZDHHC2 (V23L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326585	NM_016353.5(ZDHHC2):c.67G>C (p.Val23Leu)	LOC129999929, ZDHHC2 (V23L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264896	NM_016353.5(ZDHHC2):c.92G>T (p.Gly31Val)	LOC129999929, ZDHHC2 (G31V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance