• Mutation; HGNC; HGNC:2514; CTNNB1; Simple; p.Thr41Ala (c.121A>G); ClinVar=VCV000017580; Zygosity=Homozygous (ATCC=HTB-53; DepMap=ACH-000757).
  
• Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000012582; Zygosity=Heterozygous (PubMed=1855224; PubMed=3945555; ATCC=HTB-53; Cosmic-CLP=910851; DepMap=ACH-000757).
  
• Mutation; HGNC; HGNC:11998; TP53; None_reported; -; Zygosity=- (PubMed=10536175; PubMed=20557307).
  

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PubMed=20557307; DOI=10.1111/j.1349-7006.2010.01622.x; PMCID=PMC11158680
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PubMed=25877200; DOI=10.1038/nature14397
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PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878
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PubMed=26361996; DOI=10.1016/j.jprot.2015.09.003
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PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469
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PubMed=29444439; DOI=10.1016/j.celrep.2018.01.051; PMCID=PMC6343826
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PubMed=29681454; DOI=10.1016/j.cell.2018.03.028; PMCID=PMC5935540
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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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