G56D (p.Gly56Asp) variant of GRIN2A (Q12879)
G56D (p.Gly56Asp) in GRIN2A (Q12879) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
G56D (p.Gly56Asp) variant details
- p.Gly56Asp
- cosmic curated COSV58044
- ExAC rs769971551
- TOPMed rs769971551
- gnomAD rs769971551
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available