P29T (p.Pro29Thr) variant of GRIN2D (O15399)
P29T (p.Pro29Thr) in GRIN2D (O15399) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
P29T (p.Pro29Thr) variant details
- p.Pro29Thr
- gnomAD 19-48398477-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.265
- REVEL 0.07
- ESM-1b 0.00
- AlphaMissense 0.13
- CADD 18.20
- PolyPhen-2 0.05
- SIFT 0.32
- Population evidence available
- Structural context available
- Literature evidence available