S26G (p.Ser26Gly) variant of GRIN2D (O15399)
S26G (p.Ser26Gly) in GRIN2D (O15399) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
S26G (p.Ser26Gly) variant details
- p.Ser26Gly
- gnomAD 19-48398468-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.243
- REVEL 0.07
- ESM-1b 0.00
- AlphaMissense 0.18
- CADD 22.80
- PolyPhen-2 0.14
- SIFT 0.01
- Population evidence available
- Structural context available
- Literature evidence available