Related gene-specific medical variations for Gene (Select 65264) - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330591	NM_023079.5(UBE2Z):c.167G>C (p.Gly56Ala)	LOC105371814, LOC130061100 +1 more (G56A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185582	NM_023079.5(UBE2Z):c.76G>T (p.Gly26Cys)	LOC105371814, LOC130061100 +1 more (G26C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185580	NM_023079.5(UBE2Z):c.164C>T (p.Ala55Val)	LOC105371814, LOC130061100 +1 more (A55V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614338	NM_023079.5(UBE2Z):c.245A>G (p.His82Arg)	LOC105371814, LOC130061100 +1 more (H82R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539770	NM_023079.5(UBE2Z):c.170G>C (p.Gly57Ala)	LOC105371814, LOC130061100 +1 more (G57A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295988	NM_023079.5(UBE2Z):c.80T>G (p.Val27Gly)	LOC105371814, LOC130061100 +1 more (V27G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248331	NM_023079.5(UBE2Z):c.94G>A (p.Gly32Ser)	LOC105371814, LOC130061100 +1 more (G32S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222701	NM_023079.5(UBE2Z):c.143C>T (p.Ala48Val)	LOC105371814, LOC130061100 +1 more (A48V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance