• Mutation; HGNC; HGNC:4764; H3-3A; Simple; p.Lys28Met (c.83A>T) (H3.3K27M); ClinVar=VCV000376435; Zygosity=Unspecified (PubMed=29100338; PubMed=32229503; PubMed=34732238).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg248Trp (c.742C>T); ClinVar=VCV000012347; Zygosity=Unspecified (PubMed=29100338; PubMed=32229503; PubMed=34732238).
  

PubMed=29100338; DOI=10.18632/oncotarget.19656; PMCID=PMC5652732
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PubMed=34732238; DOI=10.1186/s40478-021-01270-y; PMCID=PMC8565061
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