G34D (p.Gly34Asp) variant of ACADVL (P49748)
G34D (p.Gly34Asp) in ACADVL (P49748) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
G34D (p.Gly34Asp) variant details
- p.Gly34Asp
- gnomAD 17-7217785-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.386
- CADD 22.00
- Most common in the Latino/Admixed American population (allele frequency 2.8e-05)
- Structural context available
- Literature evidence available