• Mutation; HGNC; HGNC:583; APC; Simple; p.Val452Serfs*7 (c.1348_1349GT[3]) (c.1354_1355delGT); ClinVar=VCV000537527; Zygosity=Homozygous (ATCC=CCL-234; Cosmic-CLP=909748; DepMap=ACH-000470).
  
• Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Arg479Gln (c.1436G>A); ClinVar=VCV000376419; Zygosity=Heterozygous (Cosmic-CLP=909748; DepMap=ACH-000470).
  
• Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Cys (c.34G>T); ClinVar=VCV000012578; Zygosity=Homozygous (PubMed=12068308; PubMed=28683746; ATCC=CCL-234; Cosmic-CLP=909748; DepMap=ACH-000470).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg248Gln (c.743G>A); ClinVar=VCV000012356; Zygosity=Homozygous (PubMed=28683746; ATCC=CCL-234; Cosmic-CLP=909748; DepMap=ACH-000470).
  

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PubMed=24755471; DOI=10.1158/0008-5472.CAN-14-0013
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PubMed=25485619; DOI=10.1038/nbt.3080
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PubMed=25926053; DOI=10.1038/ncomms8002
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PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878
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PubMed=26537799; DOI=10.1074/mcp.M115.051235; PMCID=PMC4762531
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PubMed=28683746; DOI=10.1186/s12943-017-0691-y; PMCID=PMC5498998
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PubMed=28854368; DOI=10.1016/j.celrep.2017.08.010; PMCID=PMC5583477
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PubMed=29444439; DOI=10.1016/j.celrep.2018.01.051; PMCID=PMC6343826
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PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
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PubMed=31068700; DOI=10.1038/s41586-019-1186-3; PMCID=PMC6697103
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PubMed=35839778; DOI=10.1016/j.ccell.2022.06.010; PMCID=PMC9387775
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