• Mutation; HGNC; 583; APC; Simple; p.Glu418Ter (c.1252G>T); Zygosity=Heterozygous (DepMap=ACH-000895).
  
• Mutation; HGNC; 583; APC; Simple; p.Arg856Cys (c.2566C>T); ClinVar=VCV000469755; Zygosity=Heterozygous (DepMap=ACH-000895).
  
• Mutation; HGNC; 583; APC; Simple; p.Thr1556fs*3 (c.4660_4661insA) (E1554fs); Zygosity=Heterozygous (DepMap=ACH-000895).
  
• Mutation; HGNC; 1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Heterozygous (PubMed=28683746; DepMap=ACH-000895).
  
• Mutation; HGNC; 11998; TP53; Simple; p.Ser127Pro (c.379T>C); ClinVar=VCV000934410; Zygosity=Unspecified (PubMed=28683746; DepMap=ACH-000895).
  
• Mutation; HGNC; 11998; TP53; Simple; p.Lys382Asnfs*40 (c.1146delA); ClinVar=VCV001408583; Zygosity=Unspecified (PubMed=28683746; DepMap=ACH-000895).
  

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