V1438L (p.Val1438Leu) variant of GRIN2B (Q13224)
V1438L (p.Val1438Leu) in GRIN2B (Q13224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and published literature.
V1438L (p.Val1438Leu) variant details
- p.Val1438Leu
- rs763699668
- gnomAD 12-13562926-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.383
- MetaLR 0.03
- MetaSVM -1.04
- CADD 20.20
- PolyPhen-2 0.24
- SIFT 0.15
- Population evidence available
- Literature evidence available