• Mutation; HGNC; HGNC:2514; CTNNB1; Simple; p.Gly34Val (c.101G>T); ClinVar=VCV000017582; Zygosity=Heterozygous (DepMap=ACH-000898).
  
• Mutation; HGNC; HGNC:7029; MET; Simple; p.Asp153Ala (c.458A>C); Zygosity=Heterozygous (PubMed=29435981; DepMap=ACH-000898).
  
• Mutation; HGNC; HGNC:7989; NRAS; Simple; p.Gln61Leu (c.182A>T); ClinVar=VCV000375874; Zygosity=Homozygous (DepMap=ACH-000898).
  
• Mutation; HGNC; HGNC:8975; PIK3CA; Simple; p.Pro104Arg (c.311C>G); ClinVar=VCV001480334; Zygosity=Heterozygous (DepMap=ACH-000898).
  
• Mutation; HGNC; HGNC:667; RHOA; Simple; p.Ala61Val (c.182C>T); Zygosity=Heterozygous (PubMed=34466148; DepMap=ACH-000898).
  
• Mutation; HGNC; HGNC:11998; TP53; None_reported; -; Zygosity=- (PubMed=9033653).
  

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