R1422W (p.Arg1422Trp) variant of GRIN2B (Q13224)
R1422W (p.Arg1422Trp) 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.
R1422W (p.Arg1422Trp) variant details
- p.Arg1422Trp
- rs773278200
- gnomAD 12-13562974-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.483
- MetaLR 0.08
- MetaSVM -1.13
- CADD 31.00
- PolyPhen-2 0.91
- SIFT 0.00
- Population evidence available
- Literature evidence available