GRCh38 · COSMIC v88

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
COSF166 EWSR1 7 1112 - FLI1 6 920 - 736 54.04%
COSF168 EWSR1 7 1112 - FLI1 5 854 - 345 25.33%
COSF170 EWSR1 10 1364 - FLI1 6 920 - 41 3.01%
COSF172 EWSR1 10 1364 - FLI1 5 854 - 33 2.42%
COSF177 EWSR1 7 1112 - FLI1 8 1046 - 15 1.1%
COSF181 EWSR1 7 1112 - FLI1 7 986 - 9 .66%
COSF185 EWSR1 10 1364 - FLI1 8 1046 - 4 .29%
COSF178 EWSR1 9 1331 - FLI1 4 650 - 4 .29%
COSF184 EWSR1 9 1331 - FLI1 7 986 - 3 .22%
COSF228 EWSR1 7 1112 - FLI1 9 1094 - 3 .22%
COSF1303 EWSR1 10 1364 - FLI1 7 986 - 2 .15%
COSF183 EWSR1 8 1293 - FLI1 7 986 - 1 .07%
COSF205 EWSR1 8 1293 - FLI1 6 920 - 1 .07%
COSF179 EWSR1 ? ? - FLI1 ? ? - 165 12%
Total Mutations1362100%

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