Related gene-specific medical variations for Gene (Select 89887) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258979	NM_033113.3(ZNF628):c.950C>G (p.Pro317Arg)	LOC125384540, ZNF628 (P317R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258977	NM_033113.3(ZNF628):c.1367G>T (p.Cys456Phe)	LOC125384540, ZNF628 (C456F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258976	NM_033113.3(ZNF628):c.1337C>T (p.Ala446Val)	LOC125384540, ZNF628 (A446V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197330	NM_033113.3(ZNF628):c.1637C>T (p.Ala546Val)	LOC125384540, ZNF628 (A546V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197329	NM_033113.3(ZNF628):c.1122C>G (p.His374Gln)	LOC125384540, ZNF628 (H374Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319555	NM_033113.3(ZNF628):c.1142C>G (p.Ala381Gly)	LOC125384540, ZNF628 (A381G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244952	NM_033113.3(ZNF628):c.1231G>C (p.Glu411Gln)	LOC125384540, ZNF628 (E411Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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