"Ambry Genetics"[submitter] AND "ZFP92"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2340060	NM_001136273.2(ZFP92):c.26G>C (p.Arg9Thr)	ZFP92 (R9T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2326885	NM_001136273.2(ZFP92):c.61G>C (p.Val21Leu)	ZFP92 (V21L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2325359	NM_001136273.2(ZFP92):c.61G>A (p.Val21Met)	ZFP92 (V21M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2303993	NM_001136273.2(ZFP92):c.514A>C (p.Ile172Leu)	ZFP92 (I130L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2364364	NM_001136273.2(ZFP92):c.701G>A (p.Arg234Gln)	ZFP92 (R192Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492969	NM_001136273.2(ZFP92):c.931C>G (p.Gln311Glu)	ZFP92 (Q269E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2459329	NM_001136273.2(ZFP92):c.935G>A (p.Arg312His)	ZFP92 (R270H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2287038	NM_001136273.2(ZFP92):c.943A>G (p.Ser315Gly)	ZFP92 (S273G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493055	NM_001136273.2(ZFP92):c.970G>C (p.Glu324Gln)	ZFP92 (E324Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2533435	NM_001136273.2(ZFP92):c.1073G>A (p.Gly358Asp)	ZFP92 (G358D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2354909	NM_001136273.2(ZFP92):c.1142C>T (p.Ala381Val)	ZFP92 (A339V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2362559	NM_001136273.2(ZFP92):c.1211C>T (p.Pro404Leu)	ZFP92 (P404L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance