"Ambry Genetics"[submitter] AND "ZNF560"[gene] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2207207	NM_152476.3(ZNF560):c.2348G>A (p.Arg783His)	ZNF560 (R783H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2211198	NM_152476.3(ZNF560):c.2318G>T (p.Cys773Phe)	ZNF560 (C667F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2203854	NM_152476.3(ZNF560):c.2288T>G (p.Met763Arg)	ZNF560 (M657R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2535876	NM_152476.3(ZNF560):c.2157A>T (p.Lys719Asn)	ZNF560 (K719N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2300943	NM_152476.3(ZNF560):c.2032C>T (p.His678Tyr)	ZNF560 (H678Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2211927	NM_152476.3(ZNF560):c.1871G>C (p.Gly624Ala)	ZNF560 (G518A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2323568	NM_152476.3(ZNF560):c.1867A>G (p.Thr623Ala)	ZNF560 (T517A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2591460	NM_152476.3(ZNF560):c.1834C>T (p.Arg612Cys)	ZNF560 (R506C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2329653	NM_152476.3(ZNF560):c.1750C>T (p.Arg584Cys)	ZNF560 (R478C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2337749	NM_152476.3(ZNF560):c.1604T>C (p.Met535Thr)	ZNF560 (M429T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493992	NM_152476.3(ZNF560):c.1599T>G (p.Ile533Met)	ZNF560 (I533M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2323459	NM_152476.3(ZNF560):c.1592T>C (p.Leu531Pro)	ZNF560 (L425P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2607066	NM_152476.3(ZNF560):c.1562G>T (p.Cys521Phe)	ZNF560 (C521F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2304944	NM_152476.3(ZNF560):c.1505C>A (p.Ser502Tyr)	ZNF560 (S502Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2219729	NM_152476.3(ZNF560):c.1475A>G (p.Gln492Arg)	ZNF560 (Q492R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2267471	NM_152476.3(ZNF560):c.1417T>G (p.Ser473Ala)	ZNF560 (S367A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2613497	NM_152476.3(ZNF560):c.1414T>C (p.Ser472Pro)	ZNF560 (S366P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2208774	NM_152476.3(ZNF560):c.1325T>C (p.Ile442Thr)	ZNF560 (I336T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2547090	NM_152476.3(ZNF560):c.1322T>G (p.Phe441Cys)	ZNF560 (F335C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2366307	NM_152476.3(ZNF560):c.1288A>G (p.Lys430Glu)	ZNF560 (K430E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2254115	NM_152476.3(ZNF560):c.1106C>G (p.Thr369Ser)	ZNF560 (T263S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2207361	NM_152476.3(ZNF560):c.1066G>T (p.Asp356Tyr)	ZNF560 (D250Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2466350	NM_152476.3(ZNF560):c.1016T>G (p.Val339Gly)	ZNF560 (V233G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2393045	NM_152476.3(ZNF560):c.991C>T (p.His331Tyr)	ZNF560 (H331Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2348023	NM_152476.3(ZNF560):c.941A>G (p.Gln314Arg)	ZNF560 (Q208R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2616514	NM_152476.3(ZNF560):c.936A>C (p.Lys312Asn)	ZNF560 (K312N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2350530	NM_152476.3(ZNF560):c.824G>A (p.Arg275His)	ZNF560 (R169H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2224680	NM_152476.3(ZNF560):c.785G>A (p.Arg262Lys)	ZNF560 (R156K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2363487	NM_152476.3(ZNF560):c.748G>C (p.Asp250His)	ZNF560 (D144H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2291415	NM_152476.3(ZNF560):c.637C>A (p.Leu213Ile)	ZNF560 (L107I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2207801	NM_152476.3(ZNF560):c.563C>T (p.Ala188Val)	ZNF560 (A188V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2388423	NM_152476.3(ZNF560):c.553A>G (p.Lys185Glu)	ZNF560 (K185E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2326915	NM_152476.3(ZNF560):c.488A>G (p.Glu163Gly)	ZNF560 (E57G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2343903	NM_152476.3(ZNF560):c.445G>A (p.Val149Ile)	ZNF560 (V43I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2217090	NM_152476.3(ZNF560):c.406A>G (p.Ser136Gly)	ZNF560 (S136G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2373694	NM_152476.3(ZNF560):c.239A>G (p.Asp80Gly)	ZNF560 (D80G)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2463347	NM_152476.3(ZNF560):c.182T>C (p.Val61Ala)	ZNF560 (V61A)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2327076	NM_152476.3(ZNF560):c.137A>T (p.Tyr46Phe)	ZNF560 (Y46F)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2284515	NM_152476.3(ZNF560):c.107A>T (p.Asn36Ile)	ZNF560 (N36I)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2476536	NM_152476.3(ZNF560):c.19A>G (p.Asn7Asp)	ZNF560 (N7D)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 40