R10W (p.Arg10Trp) variant of SDHB (P21912)
R10W (p.Arg10Trp) in SDHB (P21912) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
R10W (p.Arg10Trp) variant details
- p.Arg10Trp
- Ensembl rs2101551815
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available