• Mutation; HGNC; HGNC:1787; CDKN2A; Simple; c.151-1G>A; ClinVar=VCV000635365; Zygosity=Unspecified; Note=Splice acceptor mutation (PubMed=24662767).
  
• Mutation; HGNC; HGNC:1787; CDKN2A; Simple; p.Arg58Ter (c.172C>T) (p.Pro72Leu, c.215C>T); ClinVar=VCV000376310; Zygosity=Unspecified (PubMed=24662767).
  
• Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Asp154Asn (c.460G>A); Zygosity=Unspecified (PubMed=24662767).
  
• Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Cys456Ser (c.1366T>A); Zygosity=Unspecified (PubMed=24662767).
  
• Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Cys456Phe (c.1367G>T); Zygosity=Unspecified (PubMed=24662767).
  
• Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Asn1809His; Zygosity=Unspecified (PubMed=22006338).
  
• Mutation; HGNC; HGNC:7882; NOTCH2; Simple; p.Pro1913Leu (c.5738C>T); Zygosity=Unspecified (PubMed=24662767).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.His179Tyr (c.535C>T); ClinVar=VCV000127815; Zygosity=Unspecified (PubMed=21602893; PubMed=24662767).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg248Trp (c.742C>T); ClinVar=VCV000012347; Zygosity=Unspecified (PubMed=21602893; PubMed=24662767).
  

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