List of RNA-seq somatic and germline SNV callers sorted in alphabetical order. For each variant caller, the types of variants that are reported (column 2), whether DNA-RNA integrated analysis is performed (column 3), whether the tool is exclusively for RNA-seq variant calling (column 4), and whether a complete workflow including RNA-seq read mapping, variant calling, and filtering is provided (column 6) are presented. The variant callers and their core algorithms are explained in detail in Section 6.