S53I (p.Ser53Ile) variant of SCN1A (P35498)
S53I (p.Ser53Ile) 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.
S53I (p.Ser53Ile) variant details
- p.Ser53Ile
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10032
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available