• Gene deletion; HGNC; 1787; CDKN2A; Zygosity=Unspecified (PubMed=25223734).
  
• Gene fusion; HGNC; 3508; EWSR1 + HGNC; 3749; FLI1; Name(s)=EWSR1-FLI1, EWS-FLI1; Note=Type 2 fusion (Ex7/Ex5) (PubMed=11423975).
  
• Mutation; HGNC; 11998; TP53; Simple; p.Arg273Cys (c.817C>T); ClinVar=VCV000043594; Zygosity=Unspecified (PubMed=25223734).
  

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PubMed=25223734; DOI=10.1158/2159-8290.CD-14-0622; PMCID=PMC4264969
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PubMed=30971826; DOI=10.1038/s41586-019-1103-9
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DOI=10.5282/edoc.27750
Orth M.F.
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PubMed=35839778; DOI=10.1016/j.ccell.2022.06.010; PMCID=PMC9387775
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