Barely Significant
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High BRAF variant allele frequencies are associated with distinct pathological features and responsiveness to target therapy in melanoma patients.

ESMO Open · 2021 · PMC8134716 · PMID 33984673

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an increasing trendno p-value reported
The American Cancer Society reported about 100 000 new melanoma cases and 7300 estimated patient deaths in 2019 with an increasing trend of both incidence and death rates. 1 About 50% of patients carry a somatic mutation of the BRAF gene, which encodes for a serine-threonine kinase involved in the control of the MAPK pathway (BRAF/MEK/ERK). 2 The BRAF p.V600E (c. 1799T > A) pathogenic variant is detected in up to 90% of the BRAF -mu

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