A1437T (p.Ala1437Thr) variant of GRIN2B (Q13224)
A1437T (p.Ala1437Thr) 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.
A1437T (p.Ala1437Thr) variant details
- p.Ala1437Thr
- rs797045608
- gnomAD 12-13562929-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.576
- MetaLR 0.02
- MetaSVM -0.99
- CADD 23.70
- PolyPhen-2 0.19
- SIFT 0.06
- Population evidence available
- Literature evidence available