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, MOAP1 is linked to posterior cortical atrophy.