"Ambry Genetics"[submitter] AND "ZNF566"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3196772	NM_001145344.1(ZNF566):c.1049C>T (p.Ser350Phe)	LOC126862897, ZNF566 (S246F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606559	NM_001145344.1(ZNF566):c.1021T>G (p.Cys341Gly)	LOC126862897, ZNF566 (C237G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258698	NM_001145344.1(ZNF566):c.953A>G (p.Asn318Ser)	LOC126862897, ZNF566 (N214S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258697	NM_001145344.1(ZNF566):c.874T>C (p.Phe292Leu)	LOC126862897, ZNF566 (F292L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196776	NM_001145344.1(ZNF566):c.835G>C (p.Gly279Arg)	LOC126862897, ZNF566 (G279R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281581	NM_001145344.1(ZNF566):c.583A>T (p.Ile195Phe)	LOC126862897, ZNF566 (I195F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233456	NM_001145344.1(ZNF566):c.521A>G (p.Lys174Arg)	LOC126862897, ZNF566 (K175R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196775	NM_001145344.1(ZNF566):c.439G>A (p.Glu147Lys)	LOC126862897, ZNF566 (E148K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460429	NM_001145344.1(ZNF566):c.419A>G (p.Asn140Ser)	LOC126862897, ZNF566 (N140S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2226490	NM_001145344.1(ZNF566):c.410G>C (p.Gly137Ala)	LOC126862897, ZNF566 (G137A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510828	NM_001145344.1(ZNF566):c.371G>A (p.Cys124Tyr)	LOC126862897, ZNF566 (C125Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323961	NM_001145344.1(ZNF566):c.367G>A (p.Glu123Lys)	LOC126862897, ZNF566 (E19K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349197	NM_001145344.1(ZNF566):c.331C>T (p.Arg111Cys)	LOC126862897, ZNF566 (R111C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196773	NM_001145344.1(ZNF566):c.189G>T (p.Glu63Asp)	ZNF566 (E64D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance