L17P (p.Leu17Pro) variant of GRIN2D (O15399)
L17P (p.Leu17Pro) in GRIN2D (O15399) 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, published literature, and structural context.
L17P (p.Leu17Pro) variant details
- p.Leu17Pro
- gnomAD 19-48398442-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.352
- REVEL 0.21
- ESM-1b 0.29
- AlphaMissense 0.73
- CADD 23.60
- PolyPhen-2 0.02
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available