• Mutation; HGNC; 9884; RB1; Simple; p.Gln344Ter (c.1030C>T); ClinVar=VCV001771021; Zygosity=Homozygous (PubMed=26087898; ATCC=CRL-5838; Cosmic-CLP=687600; DepMap=ACH-002174).
  
• Mutation; HGNC; 11998; TP53; Simple; p.Cys176Trp (c.528C>G); ClinVar=VCV000376572; Zygosity=Homozygous (PubMed=1311061; PubMed=26087898; ATCC=CRL-5838; Cosmic-CLP=687600; DepMap=ACH-002174).
  

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