I101M (p.Ile101Met) variant of SCN10A (Q9Y5Y9)
I101M (p.Ile101Met) in SCN10A (Q9Y5Y9) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Cardiovascular phenotype. The record also includes structural context.
I101M (p.Ile101Met) variant details
- p.Ile101Met
- rs937688973
- ClinGen CA352161320
- ClinVar RCV002444001
- Ensembl rs937688973
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available