• Mutation; HGNC; HGNC:7989; NRAS; Simple; p.Gln61Arg (c.182A>G); ClinVar=VCV000013900; Zygosity=Homozygous (PubMed=1855224; ATCC=CRL-2177; Cosmic-CLP=1299062; DepMap=ACH-000890).
  
• Mutation; HGNC; HGNC:11100; SMARCA4; Simple; p.Asn774Lys (c.2322C>A); Zygosity=Homozygous (DepMap=ACH-000123).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Cys277Phe (c.830G>T); ClinVar=VCV000458567; Zygosity=Homozygous (PubMed=1855224; Cosmic-CLP=1299062; DepMap=ACH-000890).
  

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