K42N (p.Lys42Asn) variant of SCN1A (P35498)
K42N (p.Lys42Asn) 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.
K42N (p.Lys42Asn) variant details
- p.Lys42Asn
- NCI-TCGA Cosmic COSV5766
- cosmic curated COSV57663
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available