A36G (p.Ala36Gly) variant of ACADVL (P49748)
A36G (p.Ala36Gly) in ACADVL (P49748) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
A36G (p.Ala36Gly) variant details
- p.Ala36Gly
- gnomAD 17-7217797-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.204
- CADD 17.40
- Most common in the Non-Finnish European population (allele frequency 1.9e-06)
- Structural context available
- Literature evidence available