ZNF234[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic
Select item 545227	Single allele	LOC130064626, LOC130064627 +215 more	Duplication	Schizophrenia	GLikely pathogenic
Select item 2398199	NM_006630.3(ZNF234):c.19G>A (p.Gly7Arg)	ZNF234 (G7R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343435	NM_006630.3(ZNF234):c.26C>A (p.Thr9Asn)	ZNF234 (T9N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194597	NM_006630.3(ZNF234):c.53C>T (p.Thr18Ile)	ZNF234 (T18I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592415	NM_006630.3(ZNF234):c.188A>G (p.Lys63Arg)	ZNF234 (K63R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281001	NM_006630.3(ZNF234):c.259G>A (p.Glu87Lys)	ZNF234 (E87K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346928	NM_006630.3(ZNF234):c.325A>G (p.Ser109Gly)	ZNF234 (S109G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397472	NM_006630.3(ZNF234):c.367C>T (p.Arg123Trp)	ZNF234 (R123W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509741	NM_006630.3(ZNF234):c.514G>A (p.Gly172Arg)	ZNF234 (G172R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365550	NM_006630.3(ZNF234):c.653A>G (p.His218Arg)	ZNF234 (H218R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194598	NM_006630.3(ZNF234):c.755A>G (p.Lys252Arg)	ZNF234 (K252R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329145	NM_006630.3(ZNF234):c.926T>C (p.Val309Ala)	ZNF234 (V309A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194599	NM_006630.3(ZNF234):c.995G>A (p.Arg332His)	ZNF234 (R332H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2468698	NM_006630.3(ZNF234):c.1048G>A (p.Gly350Ser)	ZNF234 (G350S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194591	NM_006630.3(ZNF234):c.1117G>A (p.Val373Ile)	ZNF234 (V373I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194592	NM_006630.3(ZNF234):c.1214G>A (p.Cys405Tyr)	ZNF234 (C405Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221240	NM_006630.3(ZNF234):c.1313G>A (p.Arg438His)	ZNF234 (R438H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227883	NM_006630.3(ZNF234):c.1403G>C (p.Ser468Thr)	ZNF234 (S468T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240056	NM_006630.3(ZNF234):c.1429A>G (p.Ile477Val)	ZNF234 (I477V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194593	NM_006630.3(ZNF234):c.1464G>T (p.Glu488Asp)	ZNF234 (E488D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623414	NM_006630.3(ZNF234):c.1484G>T (p.Arg495Leu)	ZNF234 (R495L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510880	NM_006630.3(ZNF234):c.1549T>C (p.Cys517Arg)	ZNF234 (C517R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194594	NM_006630.3(ZNF234):c.1663C>T (p.Leu555Phe)	ZNF234 (L555F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194595	NM_006630.3(ZNF234):c.1684C>T (p.His562Tyr)	ZNF234 (H562Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362561	NM_006630.3(ZNF234):c.1735T>G (p.Trp579Gly)	ZNF234 (W579G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611838	NM_006630.3(ZNF234):c.1895T>G (p.Val632Gly)	ZNF234 (V632G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194596	NM_006630.3(ZNF234):c.1901G>C (p.Ser634Thr)	ZNF234 (S634T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409547	NM_006630.3(ZNF234):c.1965G>C (p.Glu655Asp)	ZNF234 (E655D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2425936	NC_000019.9:g.(?_44011002)_(45213778_?)dup	ZNF229, ZNF230 +37 more	Duplication	Ethylmalonic encephalopathy	GUncertain significance
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ACP7, ACTMAP +434 more	Copy number gain	not provided	GPathogenic
Select item 564579	GRCh37/hg19 19q13.31(chr19:44624036-44713584)x1	ZNF225, ZNF226 +1 more	Copy number loss	not provided	GUncertain significance
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	BICRA, BLOC1S3 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	A1BG, ABCA7 +1364 more	Copy number gain	See cases	GPathogenic
Select item 442437	GRCh37/hg19 19q13.31-13.32(chr19:44300416-45639540)x1	APOC1, APOC2 +39 more	Copy number loss	See cases	GUncertain significance
Select item 253540	GRCh37/hg19 19q13.2-13.32(chr19:43013365-47241534)x1	ERCC2, PPP5C +121 more	Copy number loss	See cases	GPathogenic
Select item 221402	GRCh37/hg19 19q13.31(chr19:44466919-45029206)x1	CEACAM20, ZNF112 +16 more	Copy number loss	Breast ductal adenocarcinoma	GUncertain significance
Select item 221352	chr19:44501518-45322744 complex variant	BCAM, BCL3 +22 more	Complex	Breast ductal adenocarcinoma	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 38