"Ambry Genetics"[submitter] AND "ZNF17"[gene] - ClinVar

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Items: 43

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2473197	NM_001330617.2(ZNF17):c.-32A>G	LOC130065182, ZNF17 (N2D)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2306653	NM_001330617.2(ZNF17):c.25T>G (p.Tyr9Asp)	ZNF17 (Y7D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600386	NM_001330617.2(ZNF17):c.43G>A (p.Val15Met)	ZNF17 (V15M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247741	NM_001330617.2(ZNF17):c.88G>A (p.Val30Ile)	ZNF17 (V28I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380762	NM_001330617.2(ZNF17):c.109G>A (p.Asp37Asn)	ZNF17 (D37N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304943	NM_001330617.2(ZNF17):c.116T>C (p.Met39Thr)	ZNF17 (M37T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341516	NM_001330617.2(ZNF17):c.200C>T (p.Ser67Phe)	ZNF17 (S67F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194176	NM_001330617.2(ZNF17):c.331C>T (p.Arg111Cys)	ZNF17 (R109C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527198	NM_001330617.2(ZNF17):c.341A>G (p.Lys114Arg)	ZNF17 (K112R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194177	NM_001330617.2(ZNF17):c.349C>G (p.Leu117Val)	ZNF17 (L117V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334362	NM_001330617.2(ZNF17):c.365A>G (p.His122Arg)	ZNF17 (H122R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311774	NM_001330617.2(ZNF17):c.459G>T (p.Gln153His)	ZNF17 (Q151H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194178	NM_001330617.2(ZNF17):c.560G>A (p.Ser187Asn)	ZNF17 (S185N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527325	NM_001330617.2(ZNF17):c.646G>C (p.Glu216Gln)	ZNF17 (E214Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368470	NM_001330617.2(ZNF17):c.721A>C (p.Asn241His)	ZNF17 (N239H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485519	NM_001330617.2(ZNF17):c.759T>G (p.Cys253Trp)	ZNF17 (C253W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538021	NM_001330617.2(ZNF17):c.775C>T (p.Leu259Phe)	ZNF17 (L259F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194180	NM_001330617.2(ZNF17):c.823C>G (p.Pro275Ala)	ZNF17 (P273A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370023	NM_001330617.2(ZNF17):c.835A>G (p.Ser279Gly)	ZNF17 (S277G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478513	NM_001330617.2(ZNF17):c.841T>C (p.Cys281Arg)	ZNF17 (C281R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368333	NM_001330617.2(ZNF17):c.882C>G (p.His294Gln)	ZNF17 (H292Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601911	NM_001330617.2(ZNF17):c.886A>T (p.Arg296Trp)	ZNF17 (R294W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194181	NM_001330617.2(ZNF17):c.923A>G (p.Glu308Gly)	ZNF17 (E308G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368334	NM_001330617.2(ZNF17):c.940C>G (p.Leu314Val)	ZNF17 (L314V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348240	NM_001330617.2(ZNF17):c.952C>T (p.His318Tyr)	ZNF17 (H316Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324868	NM_001330617.2(ZNF17):c.976C>G (p.His326Asp)	ZNF17 (H324D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298459	NM_001330617.2(ZNF17):c.988C>T (p.Arg330Trp)	ZNF17 (R328W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528792	NM_001330617.2(ZNF17):c.1004A>G (p.Asn335Ser)	ZNF17 (N333S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391895	NM_001330617.2(ZNF17):c.1198C>T (p.Arg400Cys)	ZNF17 (R398C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194171	NM_001330617.2(ZNF17):c.1231A>G (p.Thr411Ala)	ZNF17 (T409A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545068	NM_001330617.2(ZNF17):c.1376T>C (p.Leu459Pro)	ZNF17 (L459P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354910	NM_001330617.2(ZNF17):c.1444G>A (p.Val482Met)	ZNF17 (V482M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262234	NM_001330617.2(ZNF17):c.1501G>A (p.Glu501Lys)	ZNF17 (E499K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461669	NM_001330617.2(ZNF17):c.1578G>T (p.Arg526Ser)	ZNF17 (R524S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353381	NM_001330617.2(ZNF17):c.1580C>G (p.Pro527Arg)	ZNF17 (P527R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539154	NM_001330617.2(ZNF17):c.1645A>G (p.Asn549Asp)	ZNF17 (N547D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311057	NM_001330617.2(ZNF17):c.1670A>C (p.Glu557Ala)	ZNF17 (E557A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350139	NM_001330617.2(ZNF17):c.1803T>G (p.Ser601Arg)	ZNF17 (S599R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303804	NM_001330617.2(ZNF17):c.1846G>C (p.Glu616Gln)	ZNF17 (E614Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194173	NM_001330617.2(ZNF17):c.1882A>G (p.Ile628Val)	ZNF17 (I626V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194174	NM_001330617.2(ZNF17):c.1891C>T (p.Arg631Trp)	ZNF17 (R629W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207186	NM_001330617.2(ZNF17):c.1892G>A (p.Arg631Gln)	ZNF17 (R629Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321734	NM_001330617.2(ZNF17):c.1984C>T (p.His662Tyr)	ZNF17 (H660Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 43