"Ambry Genetics"[submitter] AND "ZNF805"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2281484	NM_001023563.4(ZNF805):c.35C>T (p.Ser12Phe)	ZNF805 (S12F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259631	NM_001023563.4(ZNF805):c.166G>C (p.Val56Leu)	ZNF805 (V56L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336862	NM_001023563.4(ZNF805):c.197A>G (p.Glu66Gly)	ZNF805 (E66G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2570252	NM_001023563.4(ZNF805):c.260A>G (p.Lys87Arg)	ZNF805 (K87R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198545	NM_001023563.4(ZNF805):c.329G>A (p.Gly110Glu)	ZNF805 (G110E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2258786	NM_001023563.4(ZNF805):c.448C>T (p.Leu150Phe)	ZNF805 (L150F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313409	NM_001023563.4(ZNF805):c.462G>A (p.Met154Ile)	ZNF805 (M154I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198546	NM_001023563.4(ZNF805):c.497G>A (p.Ser166Asn)	ZNF805 (S166N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258346	NM_001023563.4(ZNF805):c.499G>T (p.Val167Leu)	ZNF805 (V34L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296949	NM_001023563.4(ZNF805):c.516A>G (p.Ile172Met)	ZNF805 (I172M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596322	NM_001023563.4(ZNF805):c.562C>A (p.His188Asn)	ZNF805 (H188N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463305	NM_001023563.4(ZNF805):c.592G>A (p.Glu198Lys)	ZNF805 (E198K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198547	NM_001023563.4(ZNF805):c.599A>G (p.Glu200Gly)	ZNF805 (E67G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528211	NM_001023563.4(ZNF805):c.626A>G (p.Glu209Gly)	ZNF805 (E76G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2388947	NM_001023563.4(ZNF805):c.632T>C (p.Val211Ala)	ZNF805 (V78A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256688	NM_001023563.4(ZNF805):c.646C>T (p.Arg216Cys)	ZNF805 (R83C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348159	NM_001023563.4(ZNF805):c.658C>T (p.Arg220Trp)	ZNF805 (R220W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606121	NM_001023563.4(ZNF805):c.812A>G (p.Lys271Arg)	ZNF805 (K138R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198549	NM_001023563.4(ZNF805):c.911T>C (p.Leu304Ser)	ZNF805 (L304S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330211	NM_001023563.4(ZNF805):c.1106A>G (p.Lys369Arg)	ZNF805 (K369R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247267	NM_001023563.4(ZNF805):c.1130G>A (p.Gly377Glu)	ZNF805 (G377E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234643	NM_001023563.4(ZNF805):c.1150G>A (p.Ala384Thr)	ZNF805 (A251T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527003	NM_001023563.4(ZNF805):c.1265C>G (p.Thr422Ser)	ZNF805 (T289S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198543	NM_001023563.4(ZNF805):c.1400G>A (p.Arg467Lys)	ZNF805 (R467K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486488	NM_001023563.4(ZNF805):c.1414C>G (p.Arg472Gly)	ZNF805 (R472G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259632	NM_001023563.4(ZNF805):c.1420T>G (p.Phe474Val)	ZNF805 (F341V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259628	NM_001023563.4(ZNF805):c.1478A>C (p.Asn493Thr)	ZNF805 (N493T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259630	NM_001023563.4(ZNF805):c.1543G>A (p.Glu515Lys)	ZNF805 (E515K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231976	NM_001023563.4(ZNF805):c.1649G>A (p.Arg550His)	ZNF805 (R550H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358388	NM_001023563.4(ZNF805):c.1655C>T (p.Ser552Leu)	ZNF805 (S419L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259629	NM_001023563.4(ZNF805):c.1724C>T (p.Pro575Leu)	ZNF805 (P442L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523236	NM_001023563.4(ZNF805):c.1795A>G (p.Thr599Ala)	ZNF805 (T599A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350669	NM_001023563.4(ZNF805):c.1798G>A (p.Glu600Lys)	ZNF805 (E467K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198544	NM_001023563.4(ZNF805):c.1812G>C (p.Leu604Phe)	ZNF805 (L471F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 34