ZNF224[gene] - ClinVar

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Items: 69

	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 2589803	NM_001321645.3(ZNF224):c.22A>G (p.Met8Val)	ZNF224 (M8V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2239156	NM_001321645.3(ZNF224):c.24G>T (p.Met8Ile)	ZNF224 (M8I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194487	NM_001321645.3(ZNF224):c.37G>A (p.Val13Met)	ZNF224 (V13M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194490	NM_001321645.3(ZNF224):c.91A>C (p.Lys31Gln)	ZNF224 (K31Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777498	NM_001321645.3(ZNF224):c.142+10G>A	ZNF224	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3194482	NM_001321645.3(ZNF224):c.147T>G (p.His49Gln)	ZNF224 (H49Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194484	NM_001321645.3(ZNF224):c.164A>T (p.Asp55Val)	ZNF224 (D55V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471225	NM_001321645.3(ZNF224):c.214A>G (p.Ile72Val)	ZNF224 (I72V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3474678	NM_001321645.3(ZNF224):c.258G>C (p.Met86Ile)	ZNF224, ZNF225-AS1 (M86I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3474683	NM_001321645.3(ZNF224):c.283C>T (p.His95Tyr)	ZNF224, ZNF225-AS1 (H95Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2525347	NM_001321645.3(ZNF224):c.310T>C (p.Trp104Arg)	ZNF224, ZNF225-AS1 (W104R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3474680	NM_001321645.3(ZNF224):c.316A>C (p.Lys106Gln)	ZNF224, ZNF225-AS1 (K106Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3194485	NM_001321645.3(ZNF224):c.320T>C (p.Ile107Thr)	ZNF224, ZNF225-AS1 (I107T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2602241	NM_001321645.3(ZNF224):c.379G>A (p.Glu127Lys)	ZNF224, ZNF225-AS1 (E127K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2527633	NM_001321645.3(ZNF224):c.399G>T (p.Gln133His)	ZNF224, ZNF225-AS1 (Q133H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2287257	NM_001321645.3(ZNF224):c.475G>A (p.Asp159Asn)	ZNF224, ZNF225-AS1 (D159N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2377584	NM_001321645.3(ZNF224):c.527A>G (p.His176Arg)	ZNF224, ZNF225-AS1 (H176R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2461375	NM_001321645.3(ZNF224):c.611A>G (p.Tyr204Cys)	ZNF224, ZNF225-AS1 (Y204C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 788470	NM_001321645.3(ZNF224):c.641G>A (p.Ser214Asn)	ZNF224, ZNF225-AS1 (S214N)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 708001	NM_001321645.3(ZNF224):c.657G>T (p.Leu219=)	ZNF224, ZNF225-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 3194488	NM_001321645.3(ZNF224):c.662C>T (p.Thr221Ile)	ZNF224, ZNF225-AS1 (T221I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2389565	NM_001321645.3(ZNF224):c.692C>T (p.Pro231Leu)	ZNF224, ZNF225-AS1 (P231L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2350695	NM_001321645.3(ZNF224):c.796G>A (p.Gly266Arg)	ZNF224, ZNF225-AS1 (G266R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2224249	NM_001321645.3(ZNF224):c.809T>G (p.Ile270Ser)	ZNF224, ZNF225-AS1 (I270S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3474679	NM_001321645.3(ZNF224):c.820C>G (p.Gln274Glu)	ZNF224, ZNF225-AS1 (Q274E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3335177	NM_001321645.3(ZNF224):c.848C>T (p.Thr283Met)	ZNF224, ZNF225-AS1 (T283M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3194489	NM_001321645.3(ZNF224):c.853G>A (p.Glu285Lys)	ZNF224, ZNF225-AS1 (E285K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2220107	NM_001321645.3(ZNF224):c.932C>T (p.Thr311Met)	ZNF224, ZNF225-AS1 (T311M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3474681	NM_001321645.3(ZNF224):c.950G>A (p.Arg317Gln)	ZNF224, ZNF225-AS1 (R317Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3474672	NM_001321645.3(ZNF224):c.959C>T (p.Thr320Met)	ZNF224, ZNF225-AS1 (T320M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2266709	NM_001321645.3(ZNF224):c.1060A>G (p.Ile354Val)	ZNF224, ZNF225-AS1 (I354V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2508733	NM_001321645.3(ZNF224):c.1064G>A (p.Cys355Tyr)	ZNF224, ZNF225-AS1 (C355Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3194481	NM_001321645.3(ZNF224):c.1082C>T (p.Thr361Met)	ZNF224, ZNF225-AS1 (T361M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3474676	NM_001321645.3(ZNF224):c.1123A>G (p.Lys375Glu)	ZNF224, ZNF225-AS1 (K375E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 777499	NM_001321645.3(ZNF224):c.1126G>C (p.Glu376Gln)	ZNF224, ZNF225-AS1 (E376Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2375122	NM_001321645.3(ZNF224):c.1175G>A (p.Arg392Gln)	ZNF224, ZNF225-AS1 (R392Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2551185	NM_001321645.3(ZNF224):c.1214G>A (p.Cys405Tyr)	ZNF224, ZNF225-AS1 (C405Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2235912	NM_001321645.3(ZNF224):c.1220A>G (p.Lys407Arg)	ZNF224, ZNF225-AS1 (K407R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2296946	NM_001321645.3(ZNF224):c.1244G>A (p.Cys415Tyr)	ZNF224, ZNF225-AS1 (C415Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2605197	NM_001321645.3(ZNF224):c.1271G>A (p.Gly424Glu)	ZNF224, ZNF225-AS1 (G424E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 777500	NM_001321645.3(ZNF224):c.1341G>T (p.Gln447His)	ZNF224, ZNF225-AS1 (Q447H)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2369020	NM_001321645.3(ZNF224):c.1342C>T (p.Arg448Cys)	ZNF224, ZNF225-AS1 (R448C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3474675	NM_001321645.3(ZNF224):c.1345G>A (p.Val449Ile)	ZNF224, ZNF225-AS1 (V449I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3474674	NM_001321645.3(ZNF224):c.1345G>T (p.Val449Phe)	ZNF224, ZNF225-AS1 (V449F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2559475	NM_001321645.3(ZNF224):c.1346T>C (p.Val449Ala)	ZNF224, ZNF225-AS1 (V449A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 161669	NM_001321645.3(ZNF224):c.1354G>A (p.Gly452Arg)	ZNF224, ZNF225-AS1 (G452R)	Single nucleotide variant (non-coding transcript variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 3474677	NM_001321645.3(ZNF224):c.1420C>T (p.His474Tyr)	ZNF224, ZNF225-AS1 (H474Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3194483	NM_001321645.3(ZNF224):c.1505A>C (p.His502Pro)	ZNF224, ZNF225-AS1 (H502P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 769017	NM_001321645.3(ZNF224):c.1584T>C (p.Asp528=)	ZNF224, ZNF225-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2560273	NM_001321645.3(ZNF224):c.1604C>G (p.Thr535Arg)	ZNF224, ZNF225-AS1 (T535R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2552684	NM_001321645.3(ZNF224):c.1625G>T (p.Cys542Phe)	ZNF224, ZNF225-AS1 (C542F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2207412	NM_001321645.3(ZNF224):c.1823C>T (p.Ser608Phe)	ZNF224, ZNF225-AS1 (S608F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3474682	NM_001321645.3(ZNF224):c.1849C>T (p.Arg617Cys)	ZNF224, ZNF225-AS1 (R617C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3474673	NM_001321645.3(ZNF224):c.1898T>C (p.Ile633Thr)	ZNF224, ZNF225-AS1 (I633T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 724433	NM_001321645.3(ZNF224):c.1923G>C (p.Val641=)	ZNF224, ZNF225-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2204486	NM_001321645.3(ZNF224):c.1988G>C (p.Arg663Thr)	ZNF224, ZNF225-AS1 (R663T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2321676	NM_001321645.3(ZNF224):c.2047A>G (p.Arg683Gly)	ZNF224, ZNF225-AS1 (R683G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2526956	NM_001321645.3(ZNF224):c.2060T>A (p.Met687Lys)	ZNF224, ZNF225-AS1 (M687K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 769018	NM_001321645.3(ZNF224):c.2100T>C (p.Asn700=)	ZNF224, ZNF225-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2425936	NC_000019.9:g.(?_44011002)_(45213778_?)dup	CADM4, CEACAM16 +37 more	Duplication	Ethylmalonic encephalopathy	GUncertain significance
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ZNF607, ZNF780A +432 more	Copy number gain	not provided	GPathogenic
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	PGLYRP1, PGLYRP2 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	TMC4, TMED1 +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	APOC1, APOC2 +120 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: 69