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, SLIT1 is linked to posterior cortical atrophy.