• Mutation; HGNC; HGNC:7989; NRAS; Simple; p.Gln61His (c.183A>C); ClinVar=VCV000375871; Zygosity=Heterozygous (PubMed=11157491; PubMed=21173094; Cosmic-CLP=924239; DepMap=ACH-000183).
  
• Mutation; HGNC; HGNC:8975; PIK3CA; Simple; p.Glu545Lys (c.1633G>A); ClinVar=VCV000013655; Zygosity=Heterozygous (Cosmic-CLP=924239; DepMap=ACH-000183).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Ser261Thr (c.782G>C); ClinVar=VCV000187005; Zygosity=Homozygous (Cosmic-CLP=924239; DepMap=ACH-000183).
  

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PubMed=25485619; DOI=10.1038/nbt.3080
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PubMed=25688540; DOI=10.1002/cyto.a.22643
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PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878
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PubMed=30545397; DOI=10.1186/s13045-018-0679-0; PMCID=PMC6293660
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Whole-exon sequencing of human myeloma cell lines shows mutations related to myeloma patients at relapse with major hits in the DNA regulation and repair pathways.
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PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
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PubMed=30971826; DOI=10.1038/s41586-019-1103-9
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PubMed=31160637; DOI=10.1038/s41598-019-44491-x; PMCID=PMC6547646
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PubMed=32123307; DOI=10.1038/s41375-020-0785-1; PMCID=PMC7483300
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PubMed=35839778; DOI=10.1016/j.ccell.2022.06.010; PMCID=PMC9387775
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