SF3B1 Codon 626 Missense
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Associated Genetic Biomarkers
SF3B1 Codon 626 Missense is present in 0.02% of AACR GENIE cases, with breast invasive ductal carcinoma, acute myeloid leukemia with myelodysplasia-related changes, chronic lymphocytic leukemia/small lymphocytic lymphoma, endometrial endometrioid adenocarcinoma, and essential thrombocythemia having the greatest prevalence .
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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.
5. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.