E114G (p.Glu114Gly) variant of ATP13A2 (Q9NQ11)
E114G (p.Glu114Gly) in ATP13A2 (Q9NQ11) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
E114G (p.Glu114Gly) variant details
- p.Glu114Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available