S106F (p.Ser106Phe) variant of SCN1A (P35498)
S106F (p.Ser106Phe) in SCN1A (P35498) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S106F (p.Ser106Phe) variant details
- p.Ser106Phe
- NCI-TCGA Cosmic COSV5765
- cosmic curated COSV57658
- NCI-TCGA Cosmic COSV5766
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available