• Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Gly129Arg (c.385G>A); ClinVar=VCV000189484; Zygosity=Homozygous (DepMap=ACH-000370).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Cys238Ser (c.713G>C); ClinVar=VCV000376575; Zygosity=Heterozygous (DepMap=ACH-000370).
  

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