S46G (p.Ser46Gly) variant of APOC2 (Apolipoprotein C-II)
S46G (p.Ser46Gly) in APOC2 (Apolipoprotein C-II) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of Cardiovascular phenotype. The record also includes structural context.
S46G (p.Ser46Gly) variant details
- p.Ser46Gly
- rs2513572741
- ClinGen CA406292760
- ClinVar RCV004105571
- Likely benign
- Cardiovascular phenotype
- Missense
- ClinVar: Likely benign (Cardiovascular phenotype)
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available