ClinVar for Gene (Select 7711) - ClinVar

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Links from Gene

Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2613183	NM_198089.3(ZNF155):c.1477C>T (p.Leu493Phe)	ZNF155, ZNF230-DT (L493F +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2550592	NM_198089.3(ZNF155):c.1480G>C (p.Val494Leu)	ZNF155, ZNF230-DT (V494L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2537212	NM_198089.3(ZNF155):c.842T>A (p.Ile281Asn)	ZNF155 (I281N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2531387	NM_198089.3(ZNF155):c.1307G>A (p.Gly436Asp)	ZNF155, ZNF230-DT (G436D +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2526955	NM_198089.3(ZNF155):c.395C>T (p.Ser132Phe)	ZNF155 (S132F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2525655	NM_198089.3(ZNF155):c.877T>C (p.Cys293Arg)	ZNF155 (C293R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2525223	NM_198089.3(ZNF155):c.274G>A (p.Ala92Thr)	ZNF155 (A92T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2524828	NM_198089.3(ZNF155):c.1105G>A (p.Glu369Lys)	ZNF155, ZNF230-DT (E369K +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2519738	NM_198089.3(ZNF155):c.677A>G (p.His226Arg)	ZNF155 (H237R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2512733	NM_198089.3(ZNF155):c.5C>T (p.Thr2Ile)	ZNF155 (T2I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2511551	NM_198089.3(ZNF155):c.1381T>G (p.Cys461Gly)	ZNF230-DT, ZNF155 (C461G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2495711	NM_198089.3(ZNF155):c.1427G>A (p.Arg476Lys)	ZNF155, ZNF230-DT (R487K +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2489178	NM_198089.3(ZNF155):c.1406C>T (p.Ser469Leu)	ZNF155, ZNF230-DT (S469L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2466077	NM_198089.3(ZNF155):c.744T>A (p.Asn248Lys)	ZNF155 (N248K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2459406	NM_198089.3(ZNF155):c.401T>C (p.Val134Ala)	ZNF155 (V145A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2425936	NC_000019.9:g.(?_44011002)_(45213778_?)dup	ZNF229, ZNF230 +37 more	Duplication	Ethylmalonic encephalopathy	GUncertain significance
Select item 2408723	NM_198089.3(ZNF155):c.1333T>A (p.Leu445Met)	ZNF230-DT, ZNF155 (L445M +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2389180	NM_198089.3(ZNF155):c.943C>T (p.Pro315Ser)	ZNF155 (P315S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2385083	NM_198089.3(ZNF155):c.1316C>G (p.Thr439Ser)	ZNF155, ZNF230-DT (T450S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2385082	NM_198089.3(ZNF155):c.1312G>A (p.Val438Ile)	ZNF155, ZNF230-DT (V438I +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2378853	NM_198089.3(ZNF155):c.1457G>A (p.Cys486Tyr)	ZNF230-DT, ZNF155 (C486Y +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2368893	NM_198089.3(ZNF155):c.1036T>A (p.Cys346Ser)	ZNF155 (C346S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2349876	NM_198089.3(ZNF155):c.1495C>G (p.Arg499Gly)	ZNF230-DT, ZNF155 (R499G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2334929	NM_198089.3(ZNF155):c.634G>A (p.Glu212Lys)	ZNF155 (E223K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2328073	NM_198089.3(ZNF155):c.227G>A (p.Gly76Glu)	ZNF155 (G76E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2267321	NM_198089.3(ZNF155):c.1196G>A (p.Ser399Asn)	ZNF155, ZNF230-DT (S399N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2259665	NM_198089.3(ZNF155):c.149A>G (p.Gln50Arg)	ZNF155 (Q61R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2252852	NM_198089.3(ZNF155):c.822G>T (p.Gln274His)	ZNF155 (Q285H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ACP7, ACTMAP +434 more	Copy number gain	not provided	GPathogenic
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)	A1BG, ABCA7 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	LILRA4, LILRA5 +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
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	LOC130064390, LOC130064391 +2135 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 37