ZNF222[gene] - ClinVar

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Items: 32

	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 3194469	NM_001129996.2(ZNF222):c.5T>C (p.Ile2Thr)	ZNF222 (I2T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317793	NM_001129996.2(ZNF222):c.60G>T (p.Lys20Asn)	ZNF222 (K20N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600931	NM_001129996.2(ZNF222):c.130G>A (p.Asp44Asn)	ZNF222 (D44N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379084	NM_001129996.2(ZNF222):c.206T>G (p.Leu69Arg)	ZNF222 (L69R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389812	NM_001129996.2(ZNF222):c.242G>A (p.Ser81Asn)	ZNF222 (S81N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607496	NM_001129996.2(ZNF222):c.418C>A (p.Pro140Thr)	ZNF222 (P100T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319062	NM_001129996.2(ZNF222):c.458G>C (p.Arg153Thr)	ZNF222 (R113T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467859	NM_001129996.2(ZNF222):c.474G>C (p.Gln158His)	ZNF222 (Q158H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194470	NM_001129996.2(ZNF222):c.616G>A (p.Val206Ile)	ZNF222 (V166I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194471	NM_001129996.2(ZNF222):c.634T>A (p.Cys212Ser)	ZNF222 (C212S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372231	NM_001129996.2(ZNF222):c.679C>T (p.Arg227Cys)	ZNF222 (R187C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194472	NM_001129996.2(ZNF222):c.866G>T (p.Arg289Ile)	ZNF222 (R249I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261964	NM_001129996.2(ZNF222):c.940A>G (p.Arg314Gly)	ZNF222 (R274G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304133	NM_001129996.2(ZNF222):c.1010G>A (p.Arg337Lys)	ZNF222 (R297K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367075	NM_001129996.2(ZNF222):c.1058A>G (p.Tyr353Cys)	ZNF222 (Y353C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274082	NM_001129996.2(ZNF222):c.1171A>G (p.Ile391Val)	ZNF222 (I351V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408904	NM_001129996.2(ZNF222):c.1205C>T (p.Thr402Ile)	ZNF222 (T402I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2235438	NM_001129996.2(ZNF222):c.1214G>C (p.Gly405Ala)	ZNF222 (G405A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231334	NM_001129996.2(ZNF222):c.1339G>C (p.Val447Leu)	ZNF222 (V447L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369879	NM_001129996.2(ZNF222):c.1346G>A (p.Arg449Gln)	ZNF222 (R409Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259236	NM_001129996.2(ZNF222):c.1372G>A (p.Asp458Asn)	ZNF222 (D418N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286163	NM_001129996.2(ZNF222):c.1444A>G (p.Ile482Val)	ZNF222 (I442V +1 more)	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 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

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Items: 32