R52G (p.Arg52Gly) variant of GRIN2A (Q12879)
R52G (p.Arg52Gly) in GRIN2A (Q12879) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R52G (p.Arg52Gly) variant details
- p.Arg52Gly
- NCI-TCGA Cosmic COSV5805
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available