C11Y (p.Cys11Tyr) variant of SDHD (O14521)
C11Y (p.Cys11Tyr) in SDHD (O14521) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
C11Y (p.Cys11Tyr) variant details
- p.Cys11Tyr
- Ensembl rs1865620286
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available