E58S (p.Glu58Ser) variant of GRIN2A (Q12879)
E58S (p.Glu58Ser) in GRIN2A (Q12879) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
E58S (p.Glu58Ser) variant details
- p.Glu58Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available