Figure 1: The agarose gel of amplifying genomic DNA by PCR technique which use primers for eleven mutations; IVS14+1G>A, 62G>A(7), 74A>G(4), 85T>C(DPYD*9A), 812delT(4), 1003G>T(7), 1156G>T(7), 1627A>G (DPYD*5), 1714C>G, 1897delC (DPYD*3) and 2194G>A (DPYD*6), on exon 1, 8, 10, 11, 13, 14 and 17.