V39F (p.Val39Phe) variant of GRIN2B (Q13224)
V39F (p.Val39Phe) in GRIN2B (Q13224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
V39F (p.Val39Phe) variant details
- p.Val39Phe
- gnomAD 12-13437972-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.078
- CADD 4.49
- SIFT 0.03
- Population evidence available
- Structural context available
- Literature evidence available