S16R (p.Ser16Arg) variant of ACAT1 (P24752)
S16R (p.Ser16Arg) in ACAT1 (P24752) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
S16R (p.Ser16Arg) variant details
- p.Ser16Arg
- TOPMed rs1196108614
- gnomAD rs1196108614
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available