• Mutation; HGNC; HGNC:583; APC; Simple; p.Gln1131Ter (c.3391C>T); ClinVar=VCV000236590; Zygosity=Heterozygous (PubMed=24755471; DepMap=ACH-000926).
  
• Mutation; HGNC; HGNC:583; APC; Simple; p.Gln1303Ter (c.3907C>T); ClinVar=VCV001076263; Zygosity=Heterozygous (PubMed=24755471; DepMap=ACH-000926).
  
• Mutation; HGNC; HGNC:583; APC; Simple; p.Arg1463Ser (c.4389A>T); Zygosity=Heterozygous (PubMed=24755471; DepMap=ACH-000926).
  
• Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Asn581Tyr (c.1741A>T); Zygosity=Heterozygous (DepMap=ACH-000926).
  
• Mutation; HGNC; HGNC:2978; DNMT3A; Simple; p.Lys241Ter (c.721A>T); Zygosity=Heterozygous (DepMap=ACH-000926).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg213Leu (c.638G>T); ClinVar=VCV000376650; Zygosity=Homozygous (PubMed=16418264; PubMed=24755471; DepMap=ACH-000926).
  

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