In contrast to NSCLC and melanoma, which have higher levels of tumour mutational load (TML) [35, 36], glioblastoma exhibits a lower TML in most instances and infrequently shows a high TML when it is deficient in MMR protein and there is an exonuclease proof-reading domain of the DNA polymerase epsilon gene (POLE) mutation. Here, MRC1 is linked to glioblastoma.