M1L (p.Met1Leu) variant of GRIN2A (Q12879)
M1L (p.Met1Leu) in GRIN2A (Q12879) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The record also includes structural context.
M1L (p.Met1Leu) variant details
- p.Met1Leu
- rs2544033704
- ClinGen CA394715923
- ClinVar RCV003322425
- Uncertain significance
- not specified
- Missense
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available