SF3B1 Codon 663 Missense
Associated Genetic Biomarkers
SF3B1 Codon 663 Missense is present in 0.03% of AACR GENIE cases, with chronic lymphocytic leukemia/small lymphocytic lymphoma, lung adenocarcinoma, mixed phenotype acute leukemia, T/myeloid, NOS, mucosal melanoma of the head and neck, and myelodysplastic syndromes having the greatest prevalence .
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