• Mutation; HGNC; HGNC:1787; CDKN2A; Simple; c.457+1G>T; ClinVar=VCV000635367; Zygosity=Homozygous; Note=Splice donor mutation (Cosmic-CLP=687829; DepMap=ACH-000853).
  
• Mutation; HGNC; HGNC:6513; LASP1; Simple; p.Glu48Ter (c.142G>T); Zygosity=Heterozygous (Cosmic-CLP=687829; DepMap=ACH-000853).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg158Leu (c.473G>T); ClinVar=VCV000528248; Zygosity=Heterozygous (PubMed=1311061; PubMed=20557307; Cosmic-CLP=687829; DepMap=ACH-000853).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Ser215Ile (c.644G>T); ClinVar=VCV000376660; Zygosity=Heterozygous (PubMed=1311061; PubMed=20557307; Cosmic-CLP=687829; DepMap=ACH-000853).
  

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PubMed=20557307; DOI=10.1111/j.1349-7006.2010.01622.x; PMCID=PMC11158680
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PubMed=22961666; DOI=10.1158/2159-8290.CD-12-0112; PMCID=PMC3567922
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A resource for cell line authentication, annotation and quality control.
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PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878
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PubMed=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076
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PubMed=29681454; DOI=10.1016/j.cell.2018.03.028; PMCID=PMC5935540
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PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
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PubMed=31068700; DOI=10.1038/s41586-019-1186-3; PMCID=PMC6697103
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PubMed=31803961; DOI=10.1002/jcb.29564; PMCID=PMC7496084
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From clinical specimens to human cancer preclinical models -- a journey the NCI-cell line database-25 years later.
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PubMed=31978347; DOI=10.1016/j.cell.2019.12.023; PMCID=PMC7339254
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