G9W (p.Gly9Trp) variant of ALDH2 (P05091)
G9W (p.Gly9Trp) in ALDH2 (P05091) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
G9W (p.Gly9Trp) variant details
- p.Gly9Trp
- gnomAD 12-111767007-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.287
- REVEL 0.31
- CADD 16.10
- PolyPhen-2 0.40
- SIFT 0.19
- Population evidence available
- Structural context available
- Literature evidence available