• Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000012582; Zygosity=Unspecified (PubMed=28683746; DepMap=ACH-000798).
  
• Mutation; HGNC; HGNC:11876; TMPRSS2; Simple; p.Gly8Val (c.23G>T) (c.-57+99G>T); dbSNP=rs75603675; Zygosity=Heterozygous (PubMed=34339474).
  
• Mutation; HGNC; HGNC:11876; TMPRSS2; Simple; p.Val197Met (c.589G>A) (p.Val160Met, c.478G>A); dbSNP=rs12329760; Zygosity=Heterozygous (PubMed=34339474).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg248Gln (c.743G>A); ClinVar=VCV000012356; Zygosity=Unspecified (PubMed=28683746).
  

PubMed=19003396; DOI=10.1023/A:1008131428992; PMCID=PMC3449633
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