Associated Genetic Biomarkers
DNMT3A R882H is present in 0.41% of AACR GENIE cases, with acute myeloid leukemia, acute myeloid leukemia with mutated NPM1, myelodysplastic syndromes, acute myeloid leukemia with myelodysplasia-related changes, and lung adenocarcinoma 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.