PDGFRα exon 12 SNP (rs1873778), present in homozygosis in all CRC cell lines and 100% of analyzed tumor samples, has been also described in other neoplasias although in a smaller proportion of patients, including KIT and FLT3 mutation-negative core binding factor (CBFL) acute myeloid leukemias (14% of 35 patients)[25], cervical adenosquamous carcinomas (30% of 30 patients)[26] and gliomas (7% of 86 patients)[27]. The gene discussed is FLT3; the disease is cervical adenosquamous carcinoma.