• Mutation; HGNC; HGNC:16051; PARD3; Unexplicit; Ex3-7del; Zygosity=Homozygous (PubMed=20215515).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Gln38Ter (c.112C>T); Zygosity=Heterozygous (Cosmic-CLP=1240122; DepMap=ACH-001332).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Cys176Phe (c.527G>T); ClinVar=VCV000376569; Zygosity=Heterozygous (PubMed=9150362; Cosmic-CLP=1240122; DepMap=ACH-001332).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Pro177Leu (c.530C>T); ClinVar=VCV000406583; Zygosity=Heterozygous (Cosmic-CLP=1240122; DepMap=ACH-001332).
  

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