Related gene-specific medical variations for Gene (Select 9589) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3190840	NM_001270531.2(WTAP):c.860C>T (p.Thr287Met)	SOD2, WTAP (T287M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2412553	NM_001270531.2(WTAP):c.850C>T (p.Arg284Cys)	SOD2, WTAP (R284C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365972	NM_001270531.2(WTAP):c.311G>C (p.Ser104Thr)	SOD2, WTAP (S104T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339583	NM_001270531.2(WTAP):c.791A>G (p.Glu264Gly)	SOD2, WTAP (E264G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339582	NM_001270531.2(WTAP):c.790G>A (p.Glu264Lys)	SOD2, WTAP (E264K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2285043	NM_001270531.2(WTAP):c.369A>T (p.Lys123Asn)	SOD2, WTAP (K123N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214515	NM_001270531.2(WTAP):c.793G>A (p.Ala265Thr)	SOD2, WTAP (A265T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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