A32G (p.Ala32Gly) variant of MAP2K2 (P36507)
A32G (p.Ala32Gly) in MAP2K2 (P36507) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
A32G (p.Ala32Gly) variant details
- p.Ala32Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available