A16G (p.Ala16Gly) variant of ACAD9 (Q9H845)
A16G (p.Ala16Gly) in ACAD9 (Q9H845) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data, published literature, and structural context.
A16G (p.Ala16Gly) variant details
- p.Ala16Gly
- gnomAD 3-128879738-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.363
- REVEL 0.21
- CADD 8.07
- PolyPhen-2 0.01
- SIFT 0.20
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available