• Mutation; HGNC; HGNC:583; APC; Simple; p.Arg1450Ter (c.4348C>T); ClinVar=VCV000194585; Zygosity=Homozygous (ATCC=CCL-238; Cosmic-CLP=909747; DepMap=ACH-000236).
  
• Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Heterozygous (PubMed=12068308; PubMed=20570890; ATCC=CCL-238; Cosmic-CLP=909747; DepMap=ACH-000236).
  
• Mutation; HGNC; HGNC:6844; MAP2K4; Simple; p.Arg274Gly (c.820A>G); Zygosity=Homozygous (PubMed=9331070; Cosmic-CLP=909747; DepMap=ACH-000236).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Cys238Hisfs*21 (c.712_725delTGTAACAGTTCCTG); Zygosity=Heterozygous (Cosmic-CLP=909747; DepMap=ACH-000236).
  

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PubMed=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662
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PubMed=23272949; DOI=10.1186/1755-8794-5-66; PMCID=PMC3543849
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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=25877200; DOI=10.1038/nature14397
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PubMed=25926053; DOI=10.1038/ncomms8002
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PubMed=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076
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PubMed=29101300; DOI=10.15252/msb.20177701; PMCID=PMC5731344
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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=31978347; DOI=10.1016/j.cell.2019.12.023; PMCID=PMC7339254
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PubMed=35839778; DOI=10.1016/j.ccell.2022.06.010; PMCID=PMC9387775
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