Functional and conformational impact of cancer-associated mutations depends on the position and the charge of amino acid substitution

The hotspot mutations of , the most frequently mutated splicing gene in cancers, contribute to oncogenesis by corrupting the mRNA splicing Further mutations have been reported in cancers but their consequences remain unclear. Here, we screened for mutations in the vicinity of the hotspot region in tumors. We then performed prediction of the functional outcome followed by modelling of different SF3B1 mutants. We show that cancer-associated mutations present varying functional consequences that are loosely predicted by the algorithms. Analysis of the tertiary structure of SF3B1 mutants revealed that the resulting splicing errors may be due to a conformational change in SF3B1 N-terminal region, which mediates binding with other splicing factors. Our study demonstrates a varying functional impact of mutations according to the mutated codon and the amino acid substitution, implying unequal pathogenic and prognostic potentials of mutations in cancers.