• Gene fusion; HGNC; HGNC:7139; FOXO4 + HGNC; HGNC:7132; KMT2A; Name(s)=KMT2A-FOXO4, MLL-MLLT7, MLL-AFX1 (PubMed=14671638; PubMed=15843827).
  
• Mutation; HGNC; HGNC:583; APC; Simple; p.Val2194Ala (c.6581T>C); ClinVar=VCV000565658; Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:1787; CDKN2A; Simple; p.Arg80Ter (c.238C>T) (p.Pro94Leu, c.281C>T); ClinVar=VCV000009409; Zygosity=Homozygous (DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:3430; ERBB2; Simple; p.Ala586Gly (c.1757C>G); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:3495; ETV6; Simple; p.His328Tyr (c.982C>T); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Arg505Cys (c.1513C>T); ClinVar=VCV000069961; Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:3689; FGFR2; Simple; p.Met584Arg (c.1751T>G) (p.Met585Arg, c.1754T>G); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:6307; KDR; Simple; p.Arg962His (c.2885G>A); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:6342; KIT; Simple; p.Asp131Asn (c.391G>A); ClinVar=VCV000409719; Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:7029; MET; Simple; p.Ala48Thr (c.142G>A); ClinVar=VCV000454188; Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:7029; MET; Simple; p.Glu157Gly (c.470A>G); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:7325; MSH2; Simple; p.Gly221Val (c.662G>T); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Asp1852Asn (c.5554G>A); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Val2045Ile (c.6133G>A); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Gln2459Ter (c.7375C>T); Zygosity=Heterozygous (PubMed=15472075).
  
• Mutation; HGNC; HGNC:8804; PDGFRB; Simple; p.His277Gln (c.831C>A); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:9967; RET; Simple; p.Asn879Ser (c.2636A>G); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:11103; SMARCB1; Simple; p.Asn288Lys (c.864C>A); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg273Cys (c.817C>T); ClinVar=VCV000043594; Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272; DepMap=ACH-002256).
  
• Mutation; HGNC; HGNC:12796; WT1; Simple; p.Arg394Gln (c.1181G>A) (p.Arg467Gln, c.1400G>A); ClinVar=VCV000419332; Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=907272).
  

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