S118P (p.Ser118Pro) variant of ABCC9 (O60706)
S118P (p.Ser118Pro) in ABCC9 (O60706) 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.
S118P (p.Ser118Pro) variant details
- p.Ser118Pro
- rs2541827710
- ClinGen CA384129392
- ClinVar RCV002459402
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available