P37L (p.Pro37Leu) variant of SDHB (P21912)
P37L (p.Pro37Leu) in SDHB (P21912) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Pheochromocytoma; Gastrointestinal stro. The record also includes structural context.
P37L (p.Pro37Leu) variant details
- p.Pro37Leu
- TOPMed rs1324983452
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Pheochromocytoma; Gastrointestinal stro
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Pheochromocytoma; Gastr)
- UniProt: Uncertain significance
- Structural context available