G20S (p.Gly20Ser) variant of GRIN2A (Q12879)
G20S (p.Gly20Ser) in GRIN2A (Q12879) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
G20S (p.Gly20Ser) variant details
- p.Gly20Ser
- ExAC rs779149309
- TOPMed rs779149309
- gnomAD rs779149309
- Missense
- Variant Prioritization Score for Impact Estimate 0.155
- REVEL 0.07
- CADD 15.30
- PolyPhen-2 0.00
- SIFT 0.24
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available