A26T (p.Ala26Thr) variant of ACADVL (P49748)
A26T (p.Ala26Thr) in ACADVL (P49748) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
A26T (p.Ala26Thr) variant details
- p.Ala26Thr
- gnomAD 17-7217751-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.284
- CADD 18.50
- Most common in the South Asian population (allele frequency 1.3e-05)
- Structural context available
- Literature evidence available