• Mutation; HGNC; HGNC:795; ATM; Simple; p.Arg337Cys (c.1009C>T); ClinVar=VCV000127327; Zygosity=Heterozygous (Cosmic-CLP=908483; DepMap=ACH-000816).
  
• Mutation; HGNC; HGNC:9884; RB1; Simple; p.Ser576Ter (c.1727C>G); Zygosity=Homozygous (ATCC=CRL-5831; Cosmic-CLP=908483; DepMap=ACH-000816).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Thr155Asn (c.464C>A); ClinVar=VCV000406564; Zygosity=Homozygous (ATCC=CRL-5831; Cosmic-CLP=908483; DepMap=ACH-000816).
  

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PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878
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PubMed=27247353; DOI=10.1093/jnci/djw122; PMCID=PMC6279282
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PubMed=28766886; DOI=10.1002/cam4.1131; PMCID=PMC5548882
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PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
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