R18L (p.Arg18Leu) variant of ACAD9 (Q9H845)
R18L (p.Arg18Leu) in ACAD9 (Q9H845) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
R18L (p.Arg18Leu) variant details
- p.Arg18Leu
- TOPMed rs1432175650
- gnomAD rs1432175650
- Missense
- Variant Prioritization Score for Impact Estimate 0.499
- REVEL 0.49
- CADD 14.20
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available