GRCh38 · COSMIC v92

Overview

This inferred breakpoint table displays a list of all inferred breakpoints derived from a number of expressed gene fusion mRNA variants. You can see more information on the help pages.

Genes
Mutation ID 5' Partner Gene 3' Partner Gene No. of Mutations Mutation Frequency
Gene Name Last Observed Exon Inferred Breakpoint Inserted Sequence Gene Name First Observed Exon Inferred Breakpoint Inserted Sequence
COSF146 EWSR1_ENST00000397938 7 1_1112 - ERG_ENST00000442448 8 967_5034 - 27 22.13%
COSF145 EWSR1_ENST00000397938 7 1_1112 - ERG_ENST00000442448 11 1141_5034 - 15 12.3%
COSF152 EWSR1_ENST00000397938 7 1_1112 - ERG_ENST00000442448 9 1036_5034 - 5 4.1%
COSF150 EWSR1_ENST00000397938 10 1_1364 - ERG_ENST00000442448 8 967_5034 - 4 3.28%
COSF151 EWSR1_ENST00000397938 7 1_1112 - ERG_ENST00000442448 10 1093_5034 - 3 2.46%
COSF159 EWSR1_ENST00000397938 ? ? - ERG_ENST00000442448 ? ? - 68 56%
Total Mutations122100%

Tissues

Tissue based mutation frequency for all breakpoints. You can see more information on the help pages.

Primary Tissue Mutated Samples All Samples % Mutated

References

Detailed list of all the papers where this fusion has been reported. You can see more information on the help pages.

Reference Title Author Year Journal Status COSMIC Pubmed