Barely Significant
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Clinical mutational profiling and categorization of BRAF mutations in melanomas using next generation sequencing.

BMC Cancer · 2019 · PMC6612071 · PMID 31277584

Europe PMCDOI
1
hedged sentence
0.1700
closest p · 3.4× alpha
0.1700
boldest claim

The sentences

showed a trendP = 0.17not close (p > 0.1)
In old patient and young patient populations, there was no significant association of different BRAF mutations with gender, although male patients showed a trend of higher incidence of p.V600K, class-2 or class-3 mutations ( P = 0.17) and a lower incidence of p.V600E mutation ( P = 0.07) in the old patient population.

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