L9M (p.Leu9Met) variant of GRIN2A (Q12879)
L9M (p.Leu9Met) in GRIN2A (Q12879) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
L9M (p.Leu9Met) variant details
- p.Leu9Met
- gnomAD rs1364379971
- Missense
- Variant Prioritization Score for Impact Estimate 0.179
- REVEL 0.14
- CADD 21.80
- PolyPhen-2 0.88
- SIFT 0.01
- Most common in the Finnish in Finland (FIN) population (allele frequency 4.3e-05)
- Structural context available