• Mutation; HGNC; 1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Heterozygous (PubMed=12068308; ATCC=TIB-223; Cosmic-CLP=906999; DepMap=ACH-000835).
  
• Mutation; HGNC; 1787; CDKN2A; Simple; p.Leu32Arg (c.95_96TG>GT); Zygosity=Homozygous (ATCC=TIB-223; Cosmic-CLP=906999; DepMap=ACH-000835).
  
• Mutation; HGNC; 11998; TP53; Simple; p.Arg248Trp (c.742C>T); ClinVar=VCV000012347; Zygosity=Heterozygous (ATCC=TIB-223; Cosmic-CLP=906999; DepMap=ACH-000835).
  
• Mutation; HGNC; 11998; TP53; Simple; p.Gln317Ter (c.948_949delinsTT) (c.948_949CC>TT); Zygosity=Heterozygous (ATCC=TIB-223; Cosmic-CLP=906999; DepMap=ACH-000835).
  

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