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. 2020 Nov 10;11:483296. doi: 10.3389/fimmu.2020.483296

Table 1.

Recurrent TMPRSS2-ERG breakpoints in the cohort.

Breakpoint Count 5’ breakpoint 3’ breakpoint Neoepitope Expected? IAR Count
21:41508081–21:38445621 122 5′ UTR Exon 2 No NA
21:41498119–21:38445621 48 Exon 2 Exon 2 Yes DNSKMALNS EALSVVSED 37
21:41507950–21:38445621 35 Exon 1 Exon 2 Yes*** SGCEERGAA GSLISCE 22
21:41508081–21:38474121 18 5′ UTR Intron 1 No NA
21:41506445–21:38445621 18 Intron 1 Exon 2 Yes* NA
21:41508081–21:38584945 11 5′ UTR 5’UTR No NA
21:41498119–21:38474121 7 Exon 2 Intron 1 Yes** DNSKMALNS LNSIDDAQL 7
21:41508081–21:38423561 7 5′ UTR Exon 3 No NA
21:41498119–21:38423561 4 Exon 2 Exon 3 Yes*** DNSKMALNS ELS 1
21:41494356–21:38445621 3 Exon 3 Exon 2 Yes*** SPSGTVCTS RSLISCE 3

IARs from 21:41498119 to 21:38445621 and 21:41507950 to 21:38445621 are recurrent suggesting the viability of universal peptide vaccine candidates. We do not expect to see an IAR from fusions with 5′ UTR breakpoints. *TransGene cannot handle de novo splice acceptors. **An epitope will exist where the TMPRSS2 reads into the intron of ERG. ***A frameshift is seen on the ERG side of the fusion.