R19S (p.Arg19Ser) variant of GRIN2A (Q12879)
R19S (p.Arg19Ser) 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.
R19S (p.Arg19Ser) variant details
- p.Arg19Ser
- NCI-TCGA Cosmic COSV1004
- NCI-TCGA Cosmic COSV5804
- cosmic curated COSV58045
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available