Related gene-specific medical variations for Gene (Select 388561) - ClinVar - NCBI

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Links from Gene

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3198149	NM_001289951.2(ZNF761):c.1394C>G (p.Pro465Arg)	ZNF761, ZNF765-ZNF761 (P465R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198148	NM_001289951.2(ZNF761):c.121T>C (p.Tyr41His)	ZNF761, ZNF765-ZNF761 (Y41H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491532	NM_001289951.2(ZNF761):c.2113C>G (p.Leu705Val)	ZNF761, ZNF765-ZNF761 (L705V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479510	NM_001289951.2(ZNF761):c.1433A>G (p.Lys478Arg)	ZNF761, ZNF765-ZNF761 (K478R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409201	NM_001289951.2(ZNF761):c.169G>A (p.Glu57Lys)	ZNF761, ZNF765-ZNF761 (E57K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395480	NM_001289951.2(ZNF761):c.43A>G (p.Ile15Val)	ZNF761, ZNF765-ZNF761 (I15V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369598	NM_001289951.2(ZNF761):c.275A>G (p.Lys92Arg)	ZNF761, ZNF765-ZNF761 (K92R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243305	NM_001289951.2(ZNF761):c.836T>G (p.Phe279Cys)	ZNF761, ZNF765-ZNF761 (F279C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239917	NM_001289951.2(ZNF761):c.47A>C (p.Glu16Ala)	ZNF761, ZNF765-ZNF761 (E16A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance