A38S (p.Ala38Ser) variant of ACAD9 (Q9H845)
A38S (p.Ala38Ser) in ACAD9 (Q9H845) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
A38S (p.Ala38Ser) variant details
- p.Ala38Ser
- ExAC rs749279754
- gnomAD rs749279754
- Missense
- Variant Prioritization Score for Impact Estimate 0.239
- REVEL 0.23
- CADD 8.80
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available