E69K (p.Glu69Lys) variant of SCN10A (Nav1.8)
E69K (p.Glu69Lys) in SCN10A (Nav1.8) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E69K (p.Glu69Lys) variant details
- p.Glu69Lys
- NCI-TCGA Cosmic COSV7186
- cosmic curated COSV71862
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available