I1446V (p.Ile1446Val) variant of GRIN2B (Q13224)
I1446V (p.Ile1446Val) in GRIN2B (Q13224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and published literature.
I1446V (p.Ile1446Val) variant details
- p.Ile1446Val
- rs1477589166
- gnomAD 12-13562902-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.351
- MetaLR 0.01
- MetaSVM -1.01
- CADD 19.40
- PolyPhen-2 0.01
- SIFT 0.18
- Population evidence available
- Literature evidence available