S199G (p.Ser199Gly) variant of SCN5A (Q14524)
S199G (p.Ser199Gly) in SCN5A (Q14524) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S199G (p.Ser199Gly) variant details
- p.Ser199Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available