F181V (p.Phe181Val) variant of SCN5A (Q14524)
F181V (p.Phe181Val) 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.
F181V (p.Phe181Val) variant details
- p.Phe181Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available