"Ambry Genetics"[submitter] AND "ZNF565"[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2555135	NM_152477.5(ZNF565):c.1457T>A (p.Leu486His)	ZNF565 (L486H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399455	NM_152477.5(ZNF565):c.1412G>A (p.Gly471Asp)	ZNF565 (G406D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569634	NM_152477.5(ZNF565):c.1384C>G (p.Leu462Val)	ZNF565 (L462V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593900	NM_152477.5(ZNF565):c.1289G>A (p.Arg430His)	ZNF565 (R365H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461371	NM_152477.5(ZNF565):c.1189G>A (p.Gly397Arg)	ZNF565 (G332R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300860	NM_152477.5(ZNF565):c.1169C>A (p.Pro390His)	ZNF565 (P325H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361161	NM_152477.5(ZNF565):c.1006G>A (p.Glu336Lys)	ZNF565 (E336K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222887	NM_152477.5(ZNF565):c.980G>A (p.Arg327Gln)	ZNF565 (R327Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483625	NM_152477.5(ZNF565):c.869G>A (p.Arg290His)	ZNF565 (R225H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337145	NM_152477.5(ZNF565):c.838G>A (p.Val280Ile)	ZNF565 (V215I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345413	NM_152477.5(ZNF565):c.826G>A (p.Glu276Lys)	ZNF565 (E211K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392639	NM_152477.5(ZNF565):c.806A>T (p.His269Leu)	ZNF565 (H204L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362347	NM_152477.5(ZNF565):c.701G>A (p.Arg234His)	ZNF565 (R169H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542487	NM_152477.5(ZNF565):c.590G>T (p.Cys197Phe)	ZNF565 (C132F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196769	NM_152477.5(ZNF565):c.536G>A (p.Gly179Asp)	ZNF565 (G179D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362404	NM_152477.5(ZNF565):c.478A>G (p.Arg160Gly)	ZNF565 (R95G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196768	NM_152477.5(ZNF565):c.470G>A (p.Arg157His)	ZNF565 (R157H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2461831	NM_152477.5(ZNF565):c.455C>T (p.Thr152Met)	ZNF565 (T87M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216713	NM_152477.5(ZNF565):c.413T>C (p.Val138Ala)	ZNF565 (V138A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280784	NM_152477.5(ZNF565):c.391G>A (p.Glu131Lys)	ZNF565 (E131K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249692	NM_152477.5(ZNF565):c.347G>C (p.Arg116Thr)	ZNF565 (R116T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347710	NM_152477.5(ZNF565):c.335G>A (p.Gly112Asp)	ZNF565 (G112D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196767	NM_152477.5(ZNF565):c.323G>A (p.Ser108Asn)	ZNF565 (S43N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218123	NM_152477.5(ZNF565):c.283G>A (p.Gly95Arg)	ZNF565 (G95R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379909	NM_152477.5(ZNF565):c.163G>A (p.Val55Ile)	ZNF565 (V55I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3196766	NM_152477.5(ZNF565):c.131C>T (p.Ser44Leu)	ZNF565 (S44L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3196771	NM_152477.5(ZNF565):c.99G>C (p.Glu33Asp)	ZNF565 (E33D)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2329146	NM_152477.5(ZNF565):c.39A>G (p.Ile13Met)	ZNF565 (I13M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334990	NM_007145.3(ZNF146):c.343C>T (p.Leu115Phe)	ZNF146, ZNF565 (L115F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194090	NM_007145.3(ZNF146):c.471A>T (p.Lys157Asn)	ZNF146, ZNF565 (K157N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194091	NM_007145.3(ZNF146):c.778A>G (p.Arg260Gly)	ZNF146, ZNF565 (R260G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 31