The genes FOXP1, PAPPA, FLRT2, LMO7, DPYSL3, RAI14, SIK3, DAAM2, MYOM1, SLIT1, MOAP1, MAML3, NES, CBX4, and METTL3 had mutations in indolent PCa only (Table 1). Here, DAAM2 is linked to posterior cortical atrophy.