G56C (p.Gly56Cys) variant of SCN9A (Q15858)
G56C (p.Gly56Cys) in SCN9A (Q15858) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G56C (p.Gly56Cys) variant details
- p.Gly56Cys
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10031
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available