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
COSF187 EWSR1 7 1112 - WT1 8 1242 - 79 65.29%
COSF189 EWSR1 9 1331 - WT1 8 1242 - 7 5.79%
COSF191 EWSR1 10 1364 - WT1 8 1242 - 3 2.48%
COSF239 EWSR1 8 1293 - WT1 8 1242 - 2 1.65%
COSF226 EWSR1 5 732 - WT1 10 1425 - 1 .83%
COSF241 EWSR1 8 1293 - WT1 10 1425 - 1 .83%
COSF194 EWSR1 7 1112 - WT1 9 1332 - 1 .83%
COSF192 EWSR1 ? ? - 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