V13F (p.Val13Phe) variant of SCN9A (Nav1.7)
V13F (p.Val13Phe) in SCN9A (Nav1.7) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V13F (p.Val13Phe) variant details
- p.Val13Phe
- NCI-TCGA Cosmic COSV5761
- cosmic curated COSV57613
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available