Related gene-specific medical variations for Gene (Select 55625) - ClinVar - NCBI

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Links from Gene

Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3334276	NM_017740.3(ZDHHC7):c.902A>G (p.Lys301Arg)	LOC126862430, ZDHHC7 (K301R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192776	NM_017740.3(ZDHHC7):c.869T>A (p.Phe290Tyr)	LOC126862430, ZDHHC7 (F327Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192775	NM_017740.3(ZDHHC7):c.863T>C (p.Val288Ala)	LOC126862430, ZDHHC7 (V325A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192773	NM_017740.3(ZDHHC7):c.791G>A (p.Arg264Gln)	LOC126862430, ZDHHC7 (R301Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192764	NM_017740.3(ZDHHC7):c.911C>G (p.Pro304Arg)	LOC126862430, ZDHHC7 (P304R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614193	NM_017740.3(ZDHHC7):c.836C>T (p.Pro279Leu)	LOC126862430, ZDHHC7 (P279L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537948	NM_017740.3(ZDHHC7):c.832C>T (p.Pro278Ser)	LOC126862430, ZDHHC7 (P315S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286253	NM_017740.3(ZDHHC7):c.789G>T (p.Glu263Asp)	LOC126862430, ZDHHC7 (E263D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance