"Ambry Genetics"[submitter] AND "ZNF34"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3335545	NM_001286769.2(ZNF34):c.1616T>C (p.Met539Thr)	ZNF34 (M499T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195280	NM_001286769.2(ZNF34):c.1516G>A (p.Gly506Arg)	ZNF34 (G466R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285478	NM_001286769.2(ZNF34):c.1500C>G (p.His500Gln)	ZNF34 (H500Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335543	NM_001286769.2(ZNF34):c.1374G>C (p.Glu458Asp)	ZNF34 (E418D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611300	NM_001286769.2(ZNF34):c.1332C>G (p.His444Gln)	ZNF34 (H404Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195279	NM_001286769.2(ZNF34):c.1309C>G (p.Gln437Glu)	ZNF34 (Q397E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613650	NM_001286769.2(ZNF34):c.1289A>G (p.Asp430Gly)	ZNF34 (D390G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195278	NM_001286769.2(ZNF34):c.1138A>G (p.Thr380Ala)	ZNF34 (T340A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527581	NM_001286769.2(ZNF34):c.1123T>C (p.Cys375Arg)	ZNF34 (C375R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243615	NM_001286769.2(ZNF34):c.1025A>G (p.Tyr342Cys)	ZNF34 (Y302C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335544	NM_001286769.2(ZNF34):c.878A>C (p.Lys293Thr)	ZNF34 (K253T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510189	NM_001286769.2(ZNF34):c.874G>A (p.Gly292Arg)	ZNF34 (G292R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335539	NM_001286769.2(ZNF34):c.860G>A (p.Arg287Gln)	ZNF34 (R308Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512889	NM_001286769.2(ZNF34):c.830G>A (p.Arg277Gln)	ZNF34 (R237Q +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2482587	NM_001286769.2(ZNF34):c.814G>A (p.Glu272Lys)	ZNF34 (E232K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470441	NM_001286769.2(ZNF34):c.724A>G (p.Ser242Gly)	ZNF34 (S242G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335542	NM_001286769.2(ZNF34):c.697A>T (p.Ser233Cys)	ZNF34 (S193C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537491	NM_001286769.2(ZNF34):c.664A>G (p.Lys222Glu)	ZNF34 (K182E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195284	NM_001286769.2(ZNF34):c.618C>G (p.Asn206Lys)	ZNF34 (N206K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195283	NM_001286769.2(ZNF34):c.587A>G (p.His196Arg)	ZNF34 (H156R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602224	NM_001286769.2(ZNF34):c.559T>C (p.Ser187Pro)	ZNF34 (S187P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468291	NM_001286769.2(ZNF34):c.499C>T (p.Pro167Ser)	ZNF34 (P148S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217383	NM_001286769.2(ZNF34):c.451G>A (p.Gly151Arg)	ZNF34 (G172R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335541	NM_001286769.2(ZNF34):c.433G>A (p.Ala145Thr)	ZNF34 (A145T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195282	NM_001286769.2(ZNF34):c.386A>G (p.Lys129Arg)	ZNF34 (K129R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396456	NM_001286769.2(ZNF34):c.376C>A (p.His126Asn)	ZNF34 (H86N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209084	NM_001286769.2(ZNF34):c.347A>G (p.Gln116Arg)	ZNF34 (Q116R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335538	NM_001286769.2(ZNF34):c.322G>A (p.Glu108Lys)	ZNF34 (E68K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481640	NM_001286769.2(ZNF34):c.143G>T (p.Gly48Val)	ZNF34 (G69V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492010	NM_001286769.2(ZNF34):c.95G>A (p.Gly32Asp)	ZNF34 (G32D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265469	NM_001286769.2(ZNF34):c.94G>C (p.Gly32Arg)	ZNF34 (G32R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374375	NM_001286769.2(ZNF34):c.89G>A (p.Arg30His)	ZNF34 (R30H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335540	NM_001286769.2(ZNF34):c.88C>T (p.Arg30Cys)	ZNF34 (R51C +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2217224	NM_001286769.2(ZNF34):c.-53T>A	ZNF34 (L4H)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign

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Items: 34