• Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000012582; Zygosity=Heterozygous (PubMed=10353731; DepMap=ACH-000339).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Ser149Profs*21 (c.445delT); ClinVar=VCV000419519; Zygosity=Heterozygous (DepMap=ACH-000339).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg267Gln (c.800G>A); ClinVar=VCV000127823; Zygosity=Heterozygous (DepMap=ACH-000339).
  

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