Barely Significant
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Pan-cancer inference and validation of hypermorphic, hypomorphic and neomorphic mutations.

Nat Genet · 2026 · PMC12900636 · PMID 41673304

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highly significantno p-value reported
5a for an example of UCEC-specific mimicry, identifying EGFR A743T , KRAS Q61H and KDR S1347L as highly significant ARID1A Mut mimics).

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