• Mutation; HGNC; HGNC:583; APC; Simple; p.Arg283Ter (c.847C>T); ClinVar=VCV000184999; Zygosity=Unspecified (PubMed=24755471; DepMap=ACH-001460).
  
• Mutation; HGNC; HGNC:583; APC; Simple; p.Arg640Trp (c.1918C>T); ClinVar=VCV000428132; Zygosity=Unspecified (PubMed=24755471; DepMap=ACH-001460).
  
• Mutation; HGNC; HGNC:583; APC; Simple; p.Arg1450Ter (c.4348C>T); ClinVar=VCV000194585; Zygosity=Unspecified (PubMed=24755471; DepMap=ACH-001460).
  
• Mutation; HGNC; HGNC:914; B2M; Simple; p.Asp54Asn (c.160G>A); ClinVar=VCV001479725; Zygosity=Heterozygous (PubMed=8197130; DepMap=ACH-001460).
  
• Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Ala (c.35G>C); ClinVar=VCV000045122; Zygosity=Unspecified (PubMed=20570890; PubMed=24755471; DepMap=ACH-001460).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg342Ter (c.1024C>T); ClinVar=VCV000182970; Zygosity=Unspecified (PubMed=16418264; PubMed=24755471; DepMap=ACH-001460).
  

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