• Mutation; HGNC; 583; APC; Simple; p.Leu629Ter (c.1886T>G); ClinVar=VCV000429049; Zygosity=Unspecified (PubMed=24755471).
  
• Mutation; HGNC; 6407; KRAS; Simple; p.Ala146Val (c.437C>T); ClinVar=VCV000375962; Zygosity=Unspecified (PubMed=20570890; DepMap).
  
• Mutation; HGNC; 6770; SMAD4; Simple; p.Asp351His (c.1051G>C); ClinVar=VCV000375998; Zygosity=Unspecified (PubMed=24755471).
  
• Mutation; HGNC; 11998; TP53; Simple; p.Gln52Ter (c.154C>T); ClinVar=VCV001455400; Zygosity=Unspecified (PubMed=16418264).
  

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PubMed=10737795; DOI=10.1073/pnas.97.7.3352
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PubMed=16418264; DOI=10.1073/pnas.0510146103
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PubMed=18258742; DOI=10.1073/pnas.0712176105
Emaduddin M., Bicknell D.C., Bodmer W.F., Feller S.M.
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PubMed=20570890; DOI=10.1158/0008-5472.CAN-10-0192
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PubMed=25926053; DOI=10.1038/ncomms8002
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PubMed=29101300; DOI=10.15252/msb.20177701
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