• Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Arg479Gln (c.1436G>A); ClinVar=VCV000376419; Zygosity=Heterozygous (Cosmic-CLP=1290769; DepMap=ACH-000249).
  
• Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Val14Ile (c.40G>A); ClinVar=VCV000012589; Zygosity=Heterozygous (PubMed=28683746; Cosmic-CLP=1290769; DepMap=ACH-000249).
  
• Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gln61His (c.183A>C); ClinVar=VCV000177881; Zygosity=Heterozygous (PubMed=28683746; Cosmic-CLP=1290769; DepMap=ACH-000249).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Ser215Asn (c.644G>A); ClinVar=VCV000376662; Zygosity=Homozygous (PubMed=28683746; Cosmic-CLP=1290769; DepMap=ACH-000249).
  

PubMed=19003396; DOI=10.1023/A:1008131428992; PMCID=PMC3449633
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