• Mutation; HGNC; HGNC:583; APC; Simple; p.Ser1392Ter (c.4175C>A); ClinVar=VCV000188240; Zygosity=Heterozygous (Cosmic-CLP=1660036; DepMap=ACH-000991).
  
• Mutation; HGNC; HGNC:583; APC; Simple; p.Arg1450Ter (c.4348C>T); ClinVar=VCV000194585; Zygosity=Heterozygous (Cosmic-CLP=1660036; DepMap=ACH-000991).
  
• Mutation; HGNC; HGNC:583; APC; Simple; p.Arg2204Ter (c.6610C>T); ClinVar=VCV000236632; Zygosity=Heterozygous (Cosmic-CLP=1660036; DepMap=ACH-000991).
  
• Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Arg479Gln (c.1436G>A); ClinVar=VCV000376419; Zygosity=Heterozygous (Cosmic-CLP=1660036; DepMap=ACH-000991).
  
• Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Ala146Thr (c.436G>A); ClinVar=VCV000197243; Zygosity=Heterozygous (Cosmic-CLP=1660036; DepMap=ACH-000991).
  
• Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Arg130Gln (c.389G>A); ClinVar=VCV000007829; Zygosity=Heterozygous (Cosmic-CLP=1660036; DepMap=ACH-000991).
  
• Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Glu299Ter (c.895G>T); ClinVar=VCV000428263; Zygosity=Heterozygous (Cosmic-CLP=1660036; DepMap=ACH-000991).
  
• Mutation; HGNC; HGNC:11602; TBX3; Simple; p.Glu111Ter (c.331G>T); Zygosity=Heterozygous (Cosmic-CLP=1660036; DepMap=ACH-000991).
  
• Mutation; HGNC; HGNC:11602; TBX3; Simple; c.942-1G>T; Zygosity=Heterozygous; Note=Splice acceptor mutation (Cosmic-CLP=1660036; DepMap=ACH-000991).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Lys132Thr (c.395A>C); ClinVar=VCV000376627; Zygosity=Heterozygous (Cosmic-CLP=1660036; DepMap=ACH-000991).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg213Ter (c.637C>T); ClinVar=VCV000043590; Zygosity=Heterozygous (Cosmic-CLP=1660036; DepMap=ACH-000991).
  

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