Q69H (p.Gln69His) variant of ACAD9 (Q9H845)
Q69H (p.Gln69His) in ACAD9 (Q9H845) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
Q69H (p.Gln69His) variant details
- p.Gln69His
- gnomAD rs1171854557
- Missense
- Variant Prioritization Score for Impact Estimate 0.565
- REVEL 0.75
- CADD 23.20
- PolyPhen-2 0.98
- SIFT 0.05
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available