• Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Arg465Cys (c.1393C>T); ClinVar=VCV000376414; Zygosity=Heterozygous (DepMap=ACH-000963).
  
• Mutation; HGNC; HGNC:8975; PIK3CA; Simple; p.Cys420Arg (c.1258T>C); ClinVar=VCV000031945; Zygosity=Heterozygous (DepMap=ACH-000963).
  
• Mutation; HGNC; HGNC:667; RHOA; Simple; p.Arg5Gln (c.14G>A); ClinVar=VCV000376520; Zygosity=Heterozygous (PubMed=34466148; DepMap=ACH-000679).
  
• Mutation; HGNC; HGNC:667; RHOA; Simple; p.Tyr42Cys (c.125A>G); Zygosity=Heterozygous (PubMed=34466148; DepMap=ACH-000679).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Pro278His (c.833C>A); ClinVar=VCV000376646; Zygosity=Heterozygous (PubMed=16418264; DepMap=ACH-000963).
  

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