F39L (p.Phe39Leu) variant of ACADM (P11310)
F39L (p.Phe39Leu) in ACADM (P11310) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
F39L (p.Phe39Leu) variant details
- p.Phe39Leu
- TOPMed rs1458972312
- gnomAD rs1458972312
- Missense
- Variant Prioritization Score for Impact Estimate 0.657
- REVEL 0.70
- CADD 23.20
- PolyPhen-2 0.33
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available