• Mutation; HGNC; 1787; CDKN2A; Simple; p.Arg80Ter (c.238C>T) (p.Pro94Leu, c.281C>T); ClinVar=VCV000009409; Zygosity=Homozygous (PubMed=10369293; DepMap=ACH-000715).
  
• Mutation; HGNC; 11998; TP53; Simple; p.Ala159Pro (c.475G>C); ClinVar=VCV000182929; Zygosity=Homozygous (DepMap=ACH-000715).
  

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