P29S (p.Pro29Ser) variant of GRIN2D (O15399)
P29S (p.Pro29Ser) in GRIN2D (O15399) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, published literature, and structural context.
P29S (p.Pro29Ser) variant details
- p.Pro29Ser
- gnomAD 19-48398477-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.261
- REVEL 0.06
- ESM-1b 0.00
- AlphaMissense 0.13
- CADD 19.00
- PolyPhen-2 0.05
- SIFT 0.31
- Population evidence available
- Structural context available
- Literature evidence available