"Ambry Genetics"[submitter] AND "ZNF850"[gene] - ClinVar

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Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2221336	NM_001193552.2(ZNF850):c.2977G>A (p.Gly993Ser)	ZNF850 (G993S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2217091	NM_001193552.2(ZNF850):c.2750G>A (p.Arg917Gln)	ZNF850 (R917Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2223493	NM_001193552.2(ZNF850):c.2726G>A (p.Arg909His)	ZNF850 (R909H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2208993	NM_001193552.2(ZNF850):c.2642G>A (p.Arg881His)	ZNF850 (R881H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2409534	NM_001193552.2(ZNF850):c.2546C>G (p.Ser849Cys)	ZNF850 (S817C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2221335	NM_001193552.2(ZNF850):c.2524A>C (p.Ser842Arg)	ZNF850 (S842R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2523324	NM_001193552.2(ZNF850):c.2467A>G (p.Thr823Ala)	ZNF850 (T791A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2598137	NM_001193552.2(ZNF850):c.2406A>T (p.Gln802His)	ZNF850 (Q770H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455064	NM_001193552.2(ZNF850):c.2384C>T (p.Thr795Ile)	ZNF850 (T795I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2263640	NM_001193552.2(ZNF850):c.2325T>G (p.His775Gln)	ZNF850 (H743Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2244420	NM_001193552.2(ZNF850):c.2272G>A (p.Asp758Asn)	ZNF850 (D758N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2601175	NM_001193552.2(ZNF850):c.1885C>T (p.Arg629Cys)	ZNF850 (R597C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460599	NM_001193552.2(ZNF850):c.1742G>A (p.Arg581Gln)	ZNF850 (R549Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2207430	NM_001193552.2(ZNF850):c.1657G>C (p.Ala553Pro)	ZNF850 (A553P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345135	NM_001193552.2(ZNF850):c.1502G>T (p.Gly501Val)	ZNF850 (G469V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2356107	NM_001193552.2(ZNF850):c.1490G>A (p.Arg497Gln)	ZNF850 (R465Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2313146	NM_001193552.2(ZNF850):c.1481G>A (p.Arg494Gln)	ZNF850 (R462Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2561300	NM_001193552.2(ZNF850):c.1405C>T (p.Arg469Trp)	ZNF850 (R437W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2240637	NM_001193552.2(ZNF850):c.1379C>T (p.Ser460Leu)	ZNF850 (S428L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2244130	NM_001193552.2(ZNF850):c.1210T>G (p.Phe404Val)	ZNF850 (F372V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2523349	NM_001193552.2(ZNF850):c.1154G>A (p.Arg385Gln)	ZNF850 (R353Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2295926	NM_001193552.2(ZNF850):c.1046G>T (p.Gly349Val)	ZNF850 (G349V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2374377	NM_001193552.2(ZNF850):c.1007C>T (p.Pro336Leu)	ZNF850 (P336L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2615417	NM_001193552.2(ZNF850):c.998G>T (p.Gly333Val)	ZNF850 (G301V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2619395	NM_001193552.2(ZNF850):c.968C>T (p.Thr323Ile)	ZNF850 (T291I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2314133	NM_001193552.2(ZNF850):c.887T>G (p.Leu296Arg)	ZNF850 (L264R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2619224	NM_001193552.2(ZNF850):c.807T>G (p.Ile269Met)	ZNF850 (I237M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2618227	NM_001193552.2(ZNF850):c.715C>T (p.His239Tyr)	ZNF850 (H207Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471674	NM_001193552.2(ZNF850):c.674G>A (p.Cys225Tyr)	ZNF850 (C225Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2242563	NM_001193552.2(ZNF850):c.632A>G (p.Tyr211Cys)	ZNF850 (Y179C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2349198	NM_001193552.2(ZNF850):c.620A>G (p.His207Arg)	ZNF850 (H175R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2368769	NM_001193552.2(ZNF850):c.586C>T (p.Leu196Phe)	ZNF850 (L164F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355530	NM_001193552.2(ZNF850):c.580G>A (p.Glu194Lys)	ZNF850 (E194K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2243140	NM_001193552.2(ZNF850):c.485G>A (p.Arg162Gln)	ZNF850 (R130Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2390095	NM_001193552.2(ZNF850):c.287A>G (p.Tyr96Cys)	ZNF850 (Y96C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2343530	NM_001193552.2(ZNF850):c.283A>C (p.Ile95Leu)	ZNF850 (I63L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2546856	NM_001193552.2(ZNF850):c.190G>C (p.Glu64Gln)	ZNF850 (E64Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 37