A37E (p.Ala37Glu) variant of GRIN2A (Q12879)
A37E (p.Ala37Glu) 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.
A37E (p.Ala37Glu) variant details
- p.Ala37Glu
- NCI-TCGA Cosmic COSV5804
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available