A9del (p.Ala9del) variant of ACADVL (P49748)
A9del (p.Ala9del) in ACADVL (P49748) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data, published literature, and structural context.
A9del (p.Ala9del) variant details
- gnomAD 17-7217163-CGCG-C
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.565
- CADD 21.20
- Most common in the Non-Finnish European population (allele frequency 2.1e-06)
- Structural context available
- Literature evidence available