Q32K (p.Gln32Lys) variant of SCN10A (Q9Y5Y9)
Q32K (p.Gln32Lys) 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.
Q32K (p.Gln32Lys) variant details
- p.Gln32Lys
- rs2470901690
- ClinGen CA352163202
- ClinVar RCV002374119
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available