S9G (p.Ser9Gly) variant of ALDH5A1 (P51649)
S9G (p.Ser9Gly) in ALDH5A1 (P51649) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
S9G (p.Ser9Gly) variant details
- p.Ser9Gly
- gnomAD 6-24495021-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.147
- REVEL 0.14
- CADD 13.00
- PolyPhen-2 0.00
- SIFT 0.22
- Population evidence available
- Structural context available
- Literature evidence available