A38T (p.Ala38Thr) variant of ACAD9 (Q9H845)
A38T (p.Ala38Thr) in ACAD9 (Q9H845) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A38T (p.Ala38Thr) variant details
- p.Ala38Thr
- NCI-TCGA Cosmic COSV5830
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available