Q59K (p.Gln59Lys) variant of GRIN2A (Q12879)
Q59K (p.Gln59Lys) 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.
Q59K (p.Gln59Lys) variant details
- p.Gln59Lys
- NCI-TCGA Cosmic COSV1004
- cosmic curated COSV10041
- NCI-TCGA Cosmic COSV5805
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available