• Mutation; HGNC; HGNC:583; APC; Simple; p.Phe1089fs*37 (c.3266delT); Zygosity=Heterozygous (ATCC=HTB-39; Cosmic-CLP=909718; DepMap=ACH-000400).
  
• Mutation; HGNC; HGNC:583; APC; Simple; p.Pro1443fs*30 (c.4328delC); Zygosity=Heterozygous (ATCC=HTB-39; Cosmic-CLP=909718; DepMap=ACH-000400).
  
• Mutation; HGNC; HGNC:4392; GNAS; Simple; p.Arg201Cys (c.601C>T); ClinVar=VCV000015933; Zygosity=Heterozygous (Cosmic-CLP=909718; DepMap=ACH-000400).
  
• Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Val (c.35G>T); ClinVar=VCV000012583; Zygosity=Heterozygous (PubMed=12068308; PubMed=20570890; Cosmic-CLP=909718; DepMap=ACH-000400).
  
• Mutation; HGNC; HGNC:11998; TP53; None_reported; -; Zygosity=- (PubMed=16418264).
  

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PubMed=20570890; DOI=10.1158/0008-5472.CAN-10-0192; PMCID=PMC2943514
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PubMed=23272949; DOI=10.1186/1755-8794-5-66; PMCID=PMC3543849
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PubMed=24755471; DOI=10.1158/0008-5472.CAN-14-0013
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PubMed=25984343; DOI=10.1038/sdata.2014.35; PMCID=PMC4432652
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PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878
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