• Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Arg479Gln (c.1436G>A); ClinVar=VCV000376419; Zygosity=Heterozygous (Cosmic-CLP; DepMap=ACH-000996).
  
• Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Glu299Ter (c.895G>T); ClinVar=VCV000428263; Zygosity=Heterozygous (DepMap=ACH-000996).
  
• Mutation; HGNC; HGNC:9884; RB1; Simple; p.Arg552Ter (c.1654C>T); ClinVar=VCV000126840; Zygosity=Heterozygous (DepMap=ACH-000996).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Gly154Asp (c.461G>A); ClinVar=VCV000237950; Zygosity=Unspecified (PubMed=15053063).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg213Ter (c.637C>T); ClinVar=VCV000043590; Zygosity=Heterozygous (DepMap=ACH-000996).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Ser241Tyr (c.722C>A); ClinVar=VCV000376663; Zygosity=Heterozygous (DepMap=ACH-000996).
  

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