Related gene-specific medical variations for Gene (Select 57573) - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258323	NM_020813.4(ZNF471):c.1781C>T (p.Thr594Ile)	LOC126862941, ZNF471 (T594I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258322	NM_020813.4(ZNF471):c.1676C>A (p.Thr559Asn)	LOC126862941, ZNF471 (T485N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196036	NM_020813.4(ZNF471):c.1837T>C (p.Ser613Pro)	LOC126862941, ZNF471 (S613P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196035	NM_020813.4(ZNF471):c.1682A>G (p.His561Arg)	LOC126862941, ZNF471 (H487R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196034	NM_020813.4(ZNF471):c.1631A>C (p.Glu544Ala)	LOC126862941, ZNF471 (E470A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384943	NM_020813.4(ZNF471):c.1774C>G (p.Leu592Val)	LOC126862941, ZNF471 (L592V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337245	NM_020813.4(ZNF471):c.1856G>T (p.Arg619Ile)	LOC126862941, ZNF471 (R545I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279960	NM_020813.4(ZNF471):c.1624C>T (p.Pro542Ser)	LOC126862941, ZNF471 (P542S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance