• Mutation; HGNC; 7989; NRAS; Simple; p.Ala146Val (c.437C>T); Zygosity=Heterozygous (DepMap=ACH-000994).
  
• Mutation; HGNC; 9588; PTEN; Simple; p.Tyr46His (c.136T>C); ClinVar=VCV001701143; Zygosity=Heterozygous (PubMed=20944090; DepMap=ACH-000994).
  
• Mutation; HGNC; 9588; PTEN; Simple; p.Pro213Leufs (c.637_638insT) (c.637C>CT); Zygosity=Heterozygous (PubMed=20944090).
  
• Mutation; HGNC; 9588; PTEN; Simple; p.Arg233Ter (c.697C>T); ClinVar=VCV000007813; Zygosity=Heterozygous (PubMed=20944090; DepMap=ACH-000994).
  
• Mutation; HGNC; 9588; PTEN; Simple; p.Lys267Argfs*9 (c.800delA) (p.Leu265fs, c.795delA); ClinVar=VCV000092828; Zygosity=Heterozygous (PubMed=20944090; DepMap=ACH-000994).
  
• Mutation; HGNC; 11998; TP53; Simple; p.Ser95Phe (c.284C>T); ClinVar=VCV001796813; Zygosity=Heterozygous (DepMap=ACH-000994).
  
• Mutation; HGNC; 11998; TP53; Simple; p.Arg273His (c.818G>A); ClinVar=VCV000012366; Zygosity=Heterozygous (PubMed=15053063; DepMap=ACH-000994).
  

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