S19I (p.Ser19Ile) variant of SDHC (Q99643)
S19I (p.Ser19Ile) in SDHC (Q99643) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
S19I (p.Ser19Ile) variant details
- p.Ser19Ile
- rs2526332789
- ClinGen CA343359527
- ClinVar RCV003225472
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available