Figure 2.
The frequency of SF mutations in the total AML cohort. The percentage of patients with SF mutations among the total number of AML cases in this study (N = 1447) is shown. The number of cases evaluated for each gene is shown in supplemental Table 2. Cumulatively, SF mutations were identified in 22% of evaluated cases, including 148 individuals with an SRSF2 mutation, 41 patients with an SF3B1 mutation, 31 individuals with a U2AF1 mutation, and 15 patients with a ZRSR2 mutation. Furthermore, 2 patients with an SF1 mutation and 1 patient with SF3A1 and U2AF2 mutations were found.

The frequency of SF mutations in the total AML cohort. The percentage of patients with SF mutations among the total number of AML cases in this study (N = 1447) is shown. The number of cases evaluated for each gene is shown in supplemental Table 2. Cumulatively, SF mutations were identified in 22% of evaluated cases, including 148 individuals with an SRSF2 mutation, 41 patients with an SF3B1 mutation, 31 individuals with a U2AF1 mutation, and 15 patients with a ZRSR2 mutation. Furthermore, 2 patients with an SF1 mutation and 1 patient with SF3A1 and U2AF2 mutations were found.

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