Associated Genetic Biomarkers
CEBPA P23fs is present in 0.15% of AACR GENIE cases, with acute myeloid leukemia with mutated NPM1, myelodysplastic/myeloproliferative neoplasm, acute leukemia of ambiguous lineage, acute myeloid leukemia, and acute myeloid leukemia with biallelic mutations of CEBPA having the greatest prevalence .
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Liu X, Jian X, and Boerwinkle E. dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions. Human Mutation. 2011;32:894-899.
4. The AACR Project GENIE Consortium. AACR Project GENIE: powering precision medicine through an international consortium. Cancer Discovery. 2017;7(8):818-831. Dataset Version 8. This dataset does not represent the totality of the genetic landscape; see paper for more information.