• Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Gly477Ser (c.1429G>A); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Arg505Cys (c.1513C>T); ClinVar=VCV000069961; Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:3765; FLT3; Simple; p.Gly831Glu (c.2492G>A); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:6524; LCK; Simple; p.Ala353Val (c.1058C>T); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:6524; LCK; Simple; p.Pro447Leu (c.1340C>T); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:6524; LCK; Simple; p.Ala500Thr (c.1498G>A); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:7765; NF1; Simple; p.Gly1532Arg (c.4594G>A); ClinVar=VCV001462589; Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Ser2523Ter (c.7568C>A); Zygosity=Heterozygous (Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:8804; PDGFRB; Simple; p.Met772Ile (c.2316G>A); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:9967; RET; Simple; p.Cys656Phe (c.1967G>T); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:11389; STK11; Simple; p.Arg75Met (c.224G>T); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  
• Mutation; HGNC; HGNC:11389; STK11; Simple; p.Lys175Met (c.524A>T); Zygosity=Heterozygous (PubMed=22675565; Cosmic-CLP=753548; DepMap=ACH-002222).
  

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