• Mutation; HGNC; HGNC:7989; NRAS; Simple; p.Gln61Arg (c.182A>G); ClinVar=VCV000013900; Zygosity=Unspecified (PubMed=12068308).
  
• Mutation; HGNC; HGNC:11730; TERT; Simple; c.1-124C>T (c.228C>T) (C228T); Zygosity=Unspecified; Note=In promoter (PubMed=24035680).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.His365Arg (c.1094A>G); Zygosity=Unspecified (PubMed=7787250).
  

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PubMed=11921286; DOI=10.1002/gcc.10050
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PubMed=20215515; DOI=10.1158/0008-5472.CAN-09-3458; PMCID=PMC2881662
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PubMed=22460905; DOI=10.1038/nature11003; PMCID=PMC3320027
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PubMed=23401075; DOI=10.1002/path.4176
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PubMed=24367658; DOI=10.1371/journal.pone.0084411; PMCID=PMC3867501
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PubMed=24018021; DOI=10.1016/j.eururo.2013.08.052
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PubMed=24035680; DOI=10.1016/j.eururo.2013.08.057
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PubMed=25997541; DOI=10.1186/s12864-015-1450-3; PMCID=PMC4470036
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PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469
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PubMed=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076
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PubMed=29732388; DOI=10.3233/BLC-180167; PMCID=PMC5929350
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PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
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PubMed=31068700; DOI=10.1038/s41586-019-1186-3; PMCID=PMC6697103
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PubMed=31978347; DOI=10.1016/j.cell.2019.12.023; PMCID=PMC7339254
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PubMed=35839778; DOI=10.1016/j.ccell.2022.06.010; PMCID=PMC9387775
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