A13V (p.Ala13Val) variant of ACAD9 (Q9H845)
A13V (p.Ala13Val) in ACAD9 (Q9H845) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
A13V (p.Ala13Val) variant details
- p.Ala13Val
- ExAC rs781185581
- TOPMed rs781185581
- gnomAD rs781185581
- Missense
- Variant Prioritization Score for Impact Estimate 0.295
- REVEL 0.28
- CADD 15.50
- PolyPhen-2 0.04
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available