L22F (p.Leu22Phe) variant of SCN1A (P35498)
L22F (p.Leu22Phe) 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.
L22F (p.Leu22Phe) variant details
- p.Leu22Phe
- NCI-TCGA Cosmic COSV5768
- cosmic curated COSV57688
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available