C17F (p.Cys17Phe) variant of ACAD9 (Q9H845)
C17F (p.Cys17Phe) in ACAD9 (Q9H845) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
C17F (p.Cys17Phe) variant details
- p.Cys17Phe
- TOPMed rs900511320
- gnomAD rs900511320
- Missense
- Variant Prioritization Score for Impact Estimate 0.343
- REVEL 0.23
- CADD 11.60
- PolyPhen-2 0.02
- SIFT 0.22
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available