For example, Felicitas et al. [31] observed DNMT3 A mutations in only 2.6% of 193 myelodysplastic syndrome patients, while Hideki et al. [32] reported ASXL1 as the most frequent mutation (30.8%) in a cohort of SETBP1-mutated myeloid malignancies, with DNMT3 A mutations found in only 11.5%. Here, SETBP1 is linked to myelodysplastic syndrome.