• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Cys176Trp (c.528C>G); ClinVar=VCV000376572; Zygosity=Homozygous (DepMap=ACH-000690).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.His179Metfs*68 (c.535delC); Zygosity=Homozygous (DepMap=ACH-000690).
  

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