F13Y (p.Phe13Tyr) variant of SCN10A (Nav1.8)
F13Y (p.Phe13Tyr) in SCN10A (Nav1.8) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided; Cardiovascular phenotype. The record also includes structural context.
F13Y (p.Phe13Tyr) variant details
- p.Phe13Tyr
- rs981530434
- ClinGen CA72963611
- ClinVar RCV002357462
- ClinVar RCV004817018
- Uncertain significance
- not provided; Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (not provided; Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available