SF3B1 Codon 666 Missense
Associated Genetic Biomarkers
SF3B1 Codon 666 Missense is present in 0.24% of AACR GENIE cases, with myelodysplastic syndromes, acute myeloid leukemia, chronic lymphocytic leukemia/small lymphocytic lymphoma, lung adenocarcinoma, and overt primary myelofibrosis having the greatest prevalence .
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