We then contrasted demographics (age, sex, tumour location), molecular pathology (BRAF/KRAS mutation status, microsatellite instability, CMS subtype), computationally scored histopathology (mucin, stroma, tumour and glandular area per slide) and prognostic (overall survival, disease-free survival (DFS)) metrics for each subtype. The gene discussed is BRAF; the disease is neoplasm.