P1419T (p.Pro1419Thr) variant of GRIN2B (Q13224)
P1419T (p.Pro1419Thr) in GRIN2B (Q13224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and published literature.
P1419T (p.Pro1419Thr) variant details
- p.Pro1419Thr
- rs1363559243
- gnomAD 12-13562983-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.482
- MetaLR 0.02
- MetaSVM -0.96
- CADD 19.70
- PolyPhen-2 0.06
- SIFT 0.14
- Population evidence available
- Literature evidence available