A1437V (p.Ala1437Val) variant of GRIN2B (Q13224)
A1437V (p.Ala1437Val) in GRIN2B (Q13224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data and published literature.
A1437V (p.Ala1437Val) variant details
- p.Ala1437Val
- rs1948567394
- gnomAD 12-13562928-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.584
- MetaLR 0.02
- MetaSVM -0.99
- CADD 24.00
- PolyPhen-2 0.48
- SIFT 0.44
- Population evidence available
- Literature evidence available