About 40% of MM tumors can be classified by commonly observed mutations that include chromosomal translocations involving the immunoglobulin gene (Ig) with 5 recurrent chromosomal partners and oncogenes: 11q13 (CCND1); 4p16 (FGFR3 and MMSET); 6p21 (CCND3); 16q23 (MAF); and 20q11 (MAFB) [8]. This evidence concerns the gene CCND1 and Miyoshi myopathy.