A19S (p.Ala19Ser) variant of ALDH2 (P05091)
A19S (p.Ala19Ser) in ALDH2 (P05091) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
A19S (p.Ala19Ser) variant details
- p.Ala19Ser
- gnomAD rs1441105785
- Missense
- Variant Prioritization Score for Impact Estimate 0.189
- REVEL 0.12
- CADD 11.10
- PolyPhen-2 0.00
- SIFT 0.53
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.8e-05)
- Structural context available