• Mutation; HGNC; HGNC:583; APC; Simple; p.Thr1556fs*3 (c.4660_4661insA) (E1554fs); Zygosity=Heterozygous (Cosmic-CLP=1240173; DepMap=ACH-000935).
  
• Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Heterozygous (Cosmic-CLP=1240173; DepMap=ACH-000935).
  
• Mutation; HGNC; HGNC:1787; CDKN2A; Simple; p.Arg80Ter (c.238C>T) (p.Pro94Leu, c.281C>T); ClinVar=VCV000009409; Zygosity=Homozygous (Cosmic-CLP=1240173; DepMap=ACH-000935).
  
• Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Asp310Gly (c.929A>G); ClinVar=VCV000566673; Zygosity=Homozygous (Cosmic-CLP=1240173; DepMap=ACH-000935).
  
• Mutation; HGNC; HGNC:11730; TERT; Simple; c.1-146C>T (c.250C>T) (C250T); Zygosity=Unspecified; Note=In promoter (PubMed=31068700).
  
• Mutation; HGNC; HGNC:11998; TP53; None_reported; -; Zygosity=- (DepMap=ACH-000935).
  

PubMed=9813657; DOI=10.1038/sj.gt.3300690
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