R3P (p.Arg3Pro) variant of ALDH2 (P05091)
R3P (p.Arg3Pro) in ALDH2 (P05091) 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.
R3P (p.Arg3Pro) variant details
- p.Arg3Pro
- TOPMed rs1862055824
- gnomAD rs1862055824
- Missense
- Variant Prioritization Score for Impact Estimate 0.321
- REVEL 0.24
- CADD 23.70
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available