• Mutation; HGNC; HGNC:583; APC; Simple; p.Gly253Ser (c.757G>A); ClinVar=VCV000236647; Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=909251).
  
• Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Arg505Cys (c.1513C>T); ClinVar=VCV000069961; Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=909251).
  
• Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Ala1720_Val1721ins14 (c.5161_5162ins42); Zygosity=Heterozygous (PubMed=15472075).
  
• Mutation; HGNC; HGNC:7989; NRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000039648; Zygosity=Heterozygous (PubMed=10071127; PubMed=22675565; Cosmic-CLP=909251).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Glu11Gln (c.31G>C); ClinVar=VCV000041723; Zygosity=Heterozygous (PubMed=10071127; PubMed=22675565; Cosmic-CLP=909251).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg248Pro (c.743G>C); ClinVar=VCV000237954; Zygosity=Heterozygous (PubMed=10071127; PubMed=22675565; Cosmic-CLP=909251).
  

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