GRCh38 · COSMIC v94

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
COSF186 EWSR1_ENST00000397938 7 1_1112 - WT1 8 1535_3122 - 79 65.29%
COSF188 EWSR1_ENST00000397938 9 1_1331 - WT1 8 1535_3122 - 7 5.79%
COSF190 EWSR1_ENST00000397938 10 1_1364 - WT1 8 1535_3122 - 3 2.48%
COSF239 EWSR1_ENST00000397938 8 1_1293 - WT1 8 1535_3122 - 2 1.65%
COSF225 EWSR1_ENST00000397938 5 1_732 - WT1 10 1718_3122 - 1 .83%
COSF241 EWSR1_ENST00000397938 8 1_1293 - WT1 10 1718_3122 - 1 .83%
COSF193 EWSR1_ENST00000397938 7 1_1112 - WT1 9 1625_3122 - 1 .83%
COSF192 EWSR1_ENST00000397938 ? ? - WT1 ? ? - 27 22%
Total Mutations121100%

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