P13T (p.Pro13Thr) variant of GRIN2D (O15399)
P13T (p.Pro13Thr) 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.
P13T (p.Pro13Thr) variant details
- p.Pro13Thr
- gnomAD 19-48398429-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.273
- REVEL 0.10
- ESM-1b 0.00
- AlphaMissense 0.15
- CADD 23.30
- PolyPhen-2 0.74
- SIFT 0.08
- Population evidence available
- Structural context available
- Literature evidence available