• Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Tyr68His (c.202T>C); ClinVar=VCV000189474; Zygosity=Homozygous (PubMed=9787181; Cosmic-CLP=1331033; DepMap=ACH-000271).
  
• Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Asp162His (c.484G>C); Zygosity=Homozygous (PubMed=9787181; Cosmic-CLP=1331033; DepMap=ACH-000271).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; c.994-1G>A; ClinVar=VCV000142161; Zygosity=Homozygous; Note=Splice acceptor mutation (Cosmic-CLP=1331033; DepMap=ACH-000271).
  

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PubMed=29416618; DOI=10.18632/oncotarget.20378; PMCID=PMC5787470
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PubMed=30285677; DOI=10.1186/s12885-018-4840-5; PMCID=PMC6167786
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PubMed=30629668; DOI=10.1371/journal.pone.0210404; PMCID=PMC6328144
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