ClinVar for Gene (Select 7769) - ClinVar

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Links from Gene

Items: 79

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3335191	NM_001032373.2(ZNF226):c.1391C>T (p.Ala464Val)	ZNF226 (A428V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335190	NM_001032373.2(ZNF226):c.353T>C (p.Met118Thr)	ZNF226 (M118T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335189	NM_001032373.2(ZNF226):c.1153C>T (p.His385Tyr)	ZNF226 (H349Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335188	NM_001032373.2(ZNF226):c.1654G>T (p.Ala552Ser)	ZNF226 (A552S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335187	NM_001032373.2(ZNF226):c.1680G>T (p.Lys560Asn)	ZNF226 (K560N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335186	NM_001032373.2(ZNF226):c.718G>C (p.Asp240His)	ZNF226 (D204H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335185	NM_001032373.2(ZNF226):c.1127C>G (p.Ser376Cys)	ZNF226 (S340C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335184	NM_001032373.2(ZNF226):c.854G>A (p.Arg285His)	ZNF226 (R249H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3335183	NM_001032373.2(ZNF226):c.595T>C (p.Cys199Arg)	ZNF226 (C163R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335182	NM_001032373.2(ZNF226):c.1774T>C (p.Cys592Arg)	ZNF226 (C556R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194517	NM_001032373.2(ZNF226):c.827G>A (p.Gly276Glu)	ZNF226 (G240E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194516	NM_001032373.2(ZNF226):c.74T>C (p.Leu25Pro)	ZNF226 (L25P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194515	NM_001032373.2(ZNF226):c.470A>G (p.Asn157Ser)	ZNF226 (N157S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3194514	NM_001032373.2(ZNF226):c.449T>G (p.Val150Gly)	ZNF226 (V150G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194513	NM_001032373.2(ZNF226):c.325A>G (p.Asn109Asp)	ZNF226 (N73D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194512	NM_001032373.2(ZNF226):c.2370G>C (p.Lys790Asn)	ZNF226 (K790N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194511	NM_001032373.2(ZNF226):c.2330A>G (p.His777Arg)	ZNF226 (H777R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194510	NM_001032373.2(ZNF226):c.2176C>T (p.Pro726Ser)	ZNF226 (P690S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194508	NM_001032373.2(ZNF226):c.1847A>T (p.Asn616Ile)	ZNF226 (N580I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194507	NM_001032373.2(ZNF226):c.1577C>T (p.Thr526Ile)	ZNF226 (T526I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194506	NM_001032373.2(ZNF226):c.1492A>G (p.Thr498Ala)	ZNF226 (T498A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194505	NM_001032373.2(ZNF226):c.1382G>A (p.Ser461Asn)	ZNF226 (S425N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194504	NM_001032373.2(ZNF226):c.1205G>A (p.Arg402Gln)	ZNF226 (R402Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194503	NM_001032373.2(ZNF226):c.1181A>T (p.Asp394Val)	ZNF226 (D358V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194502	NM_001032373.2(ZNF226):c.1097A>T (p.Glu366Val)	ZNF226 (E330V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608762	NM_001032373.2(ZNF226):c.680A>T (p.Asn227Ile)	ZNF226 (N191I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607681	NM_001032373.2(ZNF226):c.616A>C (p.Ile206Leu)	ZNF226 (I206L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599755	NM_001032373.2(ZNF226):c.2240G>A (p.Arg747Gln)	ZNF226 (R747Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554562	NM_001032373.2(ZNF226):c.151C>G (p.Pro51Ala)	ZNF226 (P51A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545315	NM_001032373.2(ZNF226):c.1812T>G (p.Ile604Met)	ZNF226 (I604M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519626	NM_001032373.2(ZNF226):c.1793G>A (p.Arg598His)	ZNF226 (R562H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513008	NM_001032373.2(ZNF226):c.2153A>G (p.Gln718Arg)	ZNF226 (Q718R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508329	NM_001032373.2(ZNF226):c.1175A>G (p.Lys392Arg)	ZNF226 (K356R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492472	NM_001032373.2(ZNF226):c.1267G>A (p.Glu423Lys)	ZNF226 (E423K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474337	NM_001032373.2(ZNF226):c.1857G>C (p.Glu619Asp)	ZNF226 (E619D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470316	NM_001032373.2(ZNF226):c.206C>T (p.Thr69Met)	ZNF226 (T69M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467882	NM_001032373.2(ZNF226):c.37G>A (p.Val13Met)	ZNF226 (V13M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461096	NM_001032373.2(ZNF226):c.5A>G (p.Asn2Ser)	ZNF226 (N2S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2425936	NC_000019.9:g.(?_44011002)_(45213778_?)dup	CADM4, CEACAM16 +37 more	Duplication	Ethylmalonic encephalopathy	GUncertain significance
Select item 2407066	NM_001032373.2(ZNF226):c.1445A>C (p.Lys482Thr)	ZNF226 (K446T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402931	NM_001032373.2(ZNF226):c.869G>A (p.Cys290Tyr)	ZNF226 (C290Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389984	NM_001032373.2(ZNF226):c.2278T>C (p.Cys760Arg)	ZNF226 (C760R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384423	NM_001032373.2(ZNF226):c.1517A>G (p.Asn506Ser)	ZNF226 (N470S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2377789	NM_001032373.2(ZNF226):c.140T>C (p.Val47Ala)	ZNF226 (V11A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363805	NM_001032373.2(ZNF226):c.589T>C (p.Cys197Arg)	ZNF226 (C197R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360480	NM_001032373.2(ZNF226):c.706A>T (p.Ile236Phe)	ZNF226 (I236F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353868	NM_001032373.2(ZNF226):c.700A>G (p.Met234Val)	ZNF226 (M198V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353031	NM_001032373.2(ZNF226):c.191A>G (p.Gln64Arg)	ZNF226 (Q28R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2346161	NM_001032373.2(ZNF226):c.115G>A (p.Glu39Lys)	ZNF226 (E39K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337760	NM_001032373.2(ZNF226):c.736C>T (p.His246Tyr)	ZNF226 (H246Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330995	NM_001032373.2(ZNF226):c.1610G>A (p.Gly537Glu)	ZNF226 (G537E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322294	NM_001032373.2(ZNF226):c.952C>A (p.Gln318Lys)	ZNF226 (Q282K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321965	NM_001032373.2(ZNF226):c.1867G>A (p.Val623Ile)	ZNF226 (V623I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319284	NM_001032373.2(ZNF226):c.1807A>C (p.Lys603Gln)	ZNF226 (K567Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316337	NM_001032373.2(ZNF226):c.1745C>G (p.Thr582Arg)	ZNF226 (T582R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297729	NM_001032373.2(ZNF226):c.1252C>T (p.Pro418Ser)	ZNF226 (P418S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291927	NM_001032373.2(ZNF226):c.2182A>C (p.Lys728Gln)	ZNF226 (K728Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289153	NM_001032373.2(ZNF226):c.1101G>C (p.Glu367Asp)	ZNF226 (E331D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272096	NM_001032373.2(ZNF226):c.2060A>T (p.Asp687Val)	ZNF226 (D687V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266774	NM_001032373.2(ZNF226):c.613C>G (p.Pro205Ala)	ZNF226 (P169A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261143	NM_001032373.2(ZNF226):c.1786T>G (p.Phe596Val)	ZNF226 (F560V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259503	NM_001032373.2(ZNF226):c.2392G>A (p.Glu798Lys)	ZNF226 (E762K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256235	NM_001032373.2(ZNF226):c.752C>T (p.Ser251Leu)	ZNF226 (S251L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256046	NM_001032373.2(ZNF226):c.2357A>G (p.Asn786Ser)	ZNF226 (N786S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243440	NM_001032373.2(ZNF226):c.157A>C (p.Lys53Gln)	ZNF226 (K53Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243136	NM_001032373.2(ZNF226):c.553A>G (p.Asn185Asp)	ZNF226 (N149D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214989	NM_001032373.2(ZNF226):c.41C>T (p.Ala14Val)	ZNF226 (A14V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209027	NM_001032373.2(ZNF226):c.1700G>A (p.Gly567Asp)	ZNF226 (G531D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1340569	GRCh37/hg19 19q13.31(chr19:44676697-44778605)x1	ZNF226, ZNF227 +1 more	Copy number loss	not provided	GLikely benign
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ZNF607, ZNF780A +432 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 545227	Single allele	LOC130064626, LOC130064627 +215 more	Duplication	Schizophrenia	GLikely pathogenic
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
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 79