Barely Significant
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Prevalence of mutations in common tumour types in Northern England and comparable utility of national and international Trial Finders.

J Cancer Res Clin Oncol · 2023 · PMC10645649 · PMID 37702806

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highly significantno p-value reported
It is also noted that the sensitivity of the assays utilised through the TGCA data and the present cohorts differ; however, it is not likely that the differences in mutational prevalence are driven by this with highly significant variances identified.

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