S46T (p.Ser46Thr) variant of MYPN (Myopalladin)
S46T (p.Ser46Thr) in MYPN (Myopalladin) 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.
S46T (p.Ser46Thr) variant details
- p.Ser46Thr
- TOPMed rs905694884
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available