C182T (p.Cys182Thr) variant of SCN5A (Nav1.5)
C182T (p.Cys182Thr) in SCN5A (Nav1.5) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
C182T (p.Cys182Thr) variant details
- p.Cys182Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available