E38K (p.Glu38Lys) variant of SCN9A (Q15858)
E38K (p.Glu38Lys) in SCN9A (Q15858) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E38K (p.Glu38Lys) variant details
- p.Glu38Lys
- NCI-TCGA Cosmic COSV5761
- cosmic curated COSV57617
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available