"Ambry Genetics"[submitter] AND "ZNF510"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2224730	NM_014930.3(ZNF510):c.1957G>A (p.Glu653Lys)	ZNF510 (E591K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2244094	NM_014930.3(ZNF510):c.1840A>G (p.Ile614Val)	ZNF510 (I552V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2337420	NM_014930.3(ZNF510):c.1832G>A (p.Arg611Gln)	ZNF510 (R549Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247982	NM_014930.3(ZNF510):c.1756A>G (p.Thr586Ala)	ZNF510 (T524A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2225538	NM_014930.3(ZNF510):c.1748G>A (p.Arg583Gln)	ZNF510 (R583Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2396807	NM_014930.3(ZNF510):c.1747C>T (p.Arg583Trp)	ZNF510 (R583W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2362233	NM_014930.3(ZNF510):c.1721G>C (p.Cys574Ser)	ZNF510 (C512S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2616722	NM_014930.3(ZNF510):c.1622A>G (p.Glu541Gly)	ZNF510 (E479G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247522	NM_014930.3(ZNF510):c.1605G>C (p.Gln535His)	ZNF510 (Q473H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2395788	NM_014930.3(ZNF510):c.1402A>G (p.Thr468Ala)	ZNF510 (T468A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2387809	NM_014930.3(ZNF510):c.1387A>C (p.Asn463His)	ZNF510 (N401H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2369337	NM_014930.3(ZNF510):c.1328A>G (p.Gln443Arg)	ZNF510 (Q381R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2271736	NM_014930.3(ZNF510):c.1217G>A (p.Cys406Tyr)	ZNF510 (C344Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378254	NM_014930.3(ZNF510):c.1163C>T (p.Thr388Met)	ZNF510 (T326M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2288430	NM_014930.3(ZNF510):c.1149G>T (p.Lys383Asn)	ZNF510 (K383N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2229075	NM_014930.3(ZNF510):c.1087C>A (p.Pro363Thr)	ZNF510 (P301T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2304519	NM_014930.3(ZNF510):c.955G>C (p.Glu319Gln)	ZNF510 (E257Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345041	NM_014930.3(ZNF510):c.950C>T (p.Ser317Phe)	ZNF510 (S255F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2324446	NM_014930.3(ZNF510):c.946A>G (p.Lys316Glu)	ZNF510 (K254E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2253792	NM_014930.3(ZNF510):c.683A>C (p.His228Pro)	ZNF510 (H166P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2340836	NM_014930.3(ZNF510):c.682C>T (p.His228Tyr)	ZNF510 (H228Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2533135	NM_014930.3(ZNF510):c.593C>G (p.Thr198Arg)	ZNF510 (T136R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2408901	NM_014930.3(ZNF510):c.419C>A (p.Ala140Glu)	ZNF510 (A78E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2250374	NM_014930.3(ZNF510):c.337A>C (p.Asn113His)	ZNF510 (N113H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2594966	NM_014930.3(ZNF510):c.22A>G (p.Ile8Val)	ZNF510 (I8V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 25