Genomic Alterations¶
Non-synonymous mutation frequency by mRNA subtype¶
Among the TNBCs with WES data, 25,713 somatic mutations were identified, comprising 24,025 single-nucleotide variants (SNVs) and 1,688 insertions or deletions (INDELs). These tumors harbored a median of 46 nonsynonymous SNVs and 4 INDELs, which are similar to the results for the TCGA TNBC cohort.