R7G (p.Arg7Gly) variant of ALDH2 (P05091)
R7G (p.Arg7Gly) in ALDH2 (P05091) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
R7G (p.Arg7Gly) variant details
- p.Arg7Gly
- ExAC rs766577822
- TOPMed rs766577822
- gnomAD rs766577822
- Missense
- Variant Prioritization Score for Impact Estimate 0.11
- REVEL 0.11
- CADD 7.10
- PolyPhen-2 0.00
- SIFT 0.31
- Most common in the South Asian population (allele frequency 1.3e-05)
- Structural context available