"Ambry Genetics"[submitter] AND "ZNF32-AS3"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2623044	NM_006973.3(ZNF32):c.669G>T (p.Arg223Ser)	ZNF32, ZNF32-AS1 +1 more (R227S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2619969	NM_006973.3(ZNF32):c.623T>C (p.Ile208Thr)	ZNF32, ZNF32-AS1 +1 more (I183T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2546332	NM_006973.3(ZNF32):c.604G>A (p.Gly202Arg)	ZNF32, ZNF32-AS1 +1 more (G202R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2369630	NM_006973.3(ZNF32):c.454G>A (p.Glu152Lys)	ZNF32, ZNF32-AS3 +1 more (E127K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2217027	NM_006973.3(ZNF32):c.278C>T (p.Thr93Met)	ZNF32-AS3, ZNF32 +1 more (T93M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2207596	NM_006973.3(ZNF32):c.260G>A (p.Arg87Gln)	ZNF32-AS1, ZNF32 +1 more (R91Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2316598	NM_006973.3(ZNF32):c.259C>T (p.Arg87Trp)	ZNF32-AS1, ZNF32 +1 more (R91W +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2381513	NM_006973.3(ZNF32):c.221A>G (p.Gln74Arg)	ZNF32-AS1, ZNF32 +1 more (Q78R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2363242	NM_006973.3(ZNF32):c.89A>G (p.His30Arg)	ZNF32-AS1, ZNF32-AS3 +1 more (H34R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance