A26G (p.Ala26Gly) variant of ACADVL (P49748)
A26G (p.Ala26Gly) in ACADVL (P49748) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
A26G (p.Ala26Gly) variant details
- p.Ala26Gly
- TOPMed rs905475056
- gnomAD rs905475056
- Missense
- Variant Prioritization Score for Impact Estimate 0.215
- REVEL 0.18
- CADD 12.80
- PolyPhen-2 0.09
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available