A26V (p.Ala26Val) variant of ACADVL (P49748)
A26V (p.Ala26Val) in ACADVL (P49748) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
A26V (p.Ala26Val) variant details
- p.Ala26Val
- TOPMed rs905475056
- gnomAD rs905475056
- Missense
- Variant Prioritization Score for Impact Estimate 0.177
- REVEL 0.14
- CADD 8.43
- PolyPhen-2 0.00
- SIFT 0.32
- Most common in the East Asian population (allele frequency 2.6e-05)
- Structural context available