R27I (p.Arg27Ile) variant of ACAT1 (P24752)
R27I (p.Arg27Ile) in ACAT1 (P24752) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R27I (p.Arg27Ile) variant details
- p.Arg27Ile
- NCI-TCGA Cosmic COSV5492
- cosmic curated COSV54920
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available