D26Y (p.Asp26Tyr) variant of ADH1B (P00325)
D26Y (p.Asp26Tyr) in ADH1B (P00325) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
D26Y (p.Asp26Tyr) variant details
- p.Asp26Tyr
- TOPMed rs1182162110
- gnomAD rs1182162110
- Missense
- Variant Prioritization Score for Impact Estimate 0.319
- REVEL 0.12
- CADD 24.80
- PolyPhen-2 0.76
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available