R1441H (p.Arg1441His) variant of GRIN2B (Q13224)
R1441H (p.Arg1441His) in GRIN2B (Q13224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and published literature.
R1441H (p.Arg1441His) variant details
- p.Arg1441His
- rs200903876
- gnomAD 12-13562916-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.51
- MetaLR 0.03
- MetaSVM -1.09
- CADD 24.10
- PolyPhen-2 0.12
- SIFT 0.02
- Population evidence available
- Literature evidence available