E48D (p.Glu48Asp) variant of GRIN2A (Q12879)
E48D (p.Glu48Asp) in GRIN2A (Q12879) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
E48D (p.Glu48Asp) variant details
- p.Glu48Asp
- gnomAD rs1334555320
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available