A19P (p.Ala19Pro) variant of ALDH2 (P05091)
A19P (p.Ala19Pro) in ALDH2 (P05091) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
A19P (p.Ala19Pro) variant details
- p.Ala19Pro
- gnomAD rs1441105785
- Missense
- Variant Prioritization Score for Impact Estimate 0.254
- REVEL 0.22
- CADD 15.60
- PolyPhen-2 0.00
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 4.7e-06)
- Structural context available