D461G (p.Asp461Gly) variant of GRIN1 (Q05586)
D461G (p.Asp461Gly) in GRIN1 (Q05586) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
D461G (p.Asp461Gly) variant details
- p.Asp461Gly
- rs955781126
- Uncertain significance
- Missense
- EBI: ['uncertain-significance']
- UniProt: Uncertain significance
- Structural context available