• Mutation; HGNC; HGNC:1748; CDH1; Simple; p.His233Gln (c.699C>G); ClinVar=VCV000233773; Zygosity=Homozygous (PubMed=19593635).
  
• Mutation; HGNC; HGNC:8975; PIK3CA; Simple; p.His1047Arg (c.3140A>G); ClinVar=VCV000013652; Zygosity=Heterozygous (PubMed=19593635; ATCC=CRL-1902).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg342Ter (c.1024C>T); ClinVar=VCV000182970; Zygosity=Homozygous (PubMed=16541312; ATCC=CRL-1902).
  

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PubMed=20070913; DOI=10.1186/1471-2407-10-15; PMCID=PMC2836299
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PubMed=24162158; DOI=10.1007/s10549-013-2743-3; PMCID=PMC3832776
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PubMed=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076
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PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
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An interactive resource to probe genetic diversity and estimated ancestry in cancer cell lines.
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PubMed=30971826; DOI=10.1038/s41586-019-1103-9
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PubMed=31068700; DOI=10.1038/s41586-019-1186-3; PMCID=PMC6697103
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Nature 569:503-508(2019)

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