V1438M (p.Val1438Met) variant of GRIN2B (Q13224)
V1438M (p.Val1438Met) in GRIN2B (Q13224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and published literature.
V1438M (p.Val1438Met) variant details
- p.Val1438Met
- rs763699668
- gnomAD 12-13562926-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.41
- MetaLR 0.05
- MetaSVM -1.19
- CADD 23.40
- PolyPhen-2 0.76
- SIFT 0.08
- Population evidence available
- Literature evidence available