R37G (p.Arg37Gly) variant of ACAD9 (Q9H845)
R37G (p.Arg37Gly) in ACAD9 (Q9H845) is a missense change. Clinical records from EBI and UniProt describe it as pathogenic. The record also includes structural context.
R37G (p.Arg37Gly) variant details
- p.Arg37Gly
- TOPMed rs936842682
- gnomAD rs936842682
- Pathogenic
- Missense
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available