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Background: Triple‐negative breast cancer (TNBC) displays high heterogeneity. The majority of TNBC cases are characterized by high Ki‐67 expression. TNBC with low Ki‐67 expression accounts for only a small fraction of cases and has been relatively less studied. Methods: This study analyzed a large single‐center multiomics TNBC data set, combined with a single‐cell data set. The clinical, genomic, and metabolic characteristics of patients with low Ki‐67 TNBC were analyzed. Results: The clinical and pathological characteristics were analyzed in 2217 TNBC patients. Low Ki‐67 TNBC was associated with a higher patient age at diagnosis, a lower proportion of invasive ductal carcinoma, increased alterations in the PI3K‐AKT‐mTOR pathway, upregulated lipid metabolism pathways, and enhanced infiltration of M2 macrophages. High Ki‐67 TNBC exhibited a higher prevalence of TP53 gene mutations, elevated nucleotide metabolism, and increased infiltration of M1 macrophages. Conclusions: We identified specific genomic and metabolic characteristics unique to low Ki‐67 TNBC, which have implications for the development of precision therapies and patient stratification strategies. [ABSTRACT FROM AUTHOR]