S78N (p.Ser78Asn) variant of APOC2 (Apolipoprotein C-II)
S78N (p.Ser78Asn) in APOC2 (Apolipoprotein C-II) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Cardiovascular phenotype. The record also includes structural context.
S78N (p.Ser78Asn) variant details
- p.Ser78Asn
- rs2513573369
- ClinGen CA406295163
- ClinVar RCV004518528
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available