F92C (p.Phe92Cys) variant of SCN10A (Nav1.8)
F92C (p.Phe92Cys) in SCN10A (Nav1.8) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
F92C (p.Phe92Cys) variant details
- p.Phe92Cys
- NCI-TCGA Cosmic COSV1014
- cosmic curated COSV10147
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.96
- MetaSVM 1.10
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available