Related gene-specific medical variations for Gene (Select 374655) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259319	NM_198526.4(ZNF710):c.1933G>A (p.Ala645Thr)	ZNF710, ZNF710-AS1 (A645T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301437	NM_198526.4(ZNF710):c.1840C>G (p.Leu614Val)	ZNF710, ZNF710-AS1 (L614V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241469	NM_198526.4(ZNF710):c.1858T>G (p.Ser620Ala)	ZNF710, ZNF710-AS1 (S620A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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