S26N (p.Ser26Asn) variant of GRIN2D (O15399)
S26N (p.Ser26Asn) in GRIN2D (O15399) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
S26N (p.Ser26Asn) variant details
- p.Ser26Asn
- gnomAD 19-48398469-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.334
- REVEL 0.05
- ESM-1b 1.00
- AlphaMissense 0.54
- CADD 22.40
- PolyPhen-2 0.10
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available