"Ambry Genetics"[submitter] AND "ZNF704"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3197866	NM_001033723.3(ZNF704):c.1186A>G (p.Met396Val)	LOC126860428, ZNF704 (M396V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547912	NM_001033723.3(ZNF704):c.1132C>T (p.Pro378Ser)	LOC126860428, ZNF704 (P378S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197865	NM_001033723.3(ZNF704):c.1033G>A (p.Val345Met)	ZNF704 (V519M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391271	NM_001033723.3(ZNF704):c.973A>G (p.Asn325Asp)	ZNF704 (N499D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591702	NM_001033723.3(ZNF704):c.827C>G (p.Thr276Arg)	ZNF704 (T276R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509762	NM_001033723.3(ZNF704):c.650T>A (p.Ile217Asn)	ZNF704 (I217N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477028	NM_001033723.3(ZNF704):c.382A>G (p.Ser128Gly)	ZNF704 (S128G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197868	NM_001033723.3(ZNF704):c.365C>T (p.Pro122Leu)	ZNF704 (P296L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206327	NM_001033723.3(ZNF704):c.316C>T (p.Arg106Trp)	ZNF704 (R106W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555931	NM_001033723.3(ZNF704):c.278G>C (p.Ser93Thr)	ZNF704 (S267T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197867	NM_001033723.3(ZNF704):c.259G>A (p.Ala87Thr)	ZNF704 (A261T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240347	NM_001033723.3(ZNF704):c.89A>G (p.Glu30Gly)	ZNF704 (E204G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508023	NM_001033723.3(ZNF704):c.82A>G (p.Met28Val)	ZNF704 (M202V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513997	NM_001033723.3(ZNF704):c.53T>A (p.Met18Lys)	ZNF704 (M18K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2203837	NM_001033723.3(ZNF704):c.14T>G (p.Phe5Cys)	ZNF704 (F179C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance