C17Y (p.Cys17Tyr) variant of ACAD9 (Q9H845)
C17Y (p.Cys17Tyr) in ACAD9 (Q9H845) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
C17Y (p.Cys17Tyr) variant details
- p.Cys17Tyr
- TOPMed rs900511320
- gnomAD rs900511320
- Missense
- Variant Prioritization Score for Impact Estimate 0.369
- REVEL 0.28
- CADD 10.40
- PolyPhen-2 0.02
- SIFT 0.34
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available