SF3B1 and myeloid neoplasm: Concurrent next generation sequencing looking for gene aberrations associated with myeloid neoplasms detected three different alterations; ETV6 exon 3 inframe insertion W69dup (allele variant frequency 42%), a JAK2 R564L point mutation (allele variant frequency 46%), and a SF3B1 E622D point mutation (allele variant frequency 40%).