"Ambry Genetics"[submitter] AND "ZNF230-DT"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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 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 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 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 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 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 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 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