A37G (p.Ala37Gly) variant of GRIN2A (Q12879)
A37G (p.Ala37Gly) 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.
A37G (p.Ala37Gly) variant details
- p.Ala37Gly
- NCI-TCGA Cosmic COSV5804
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available