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
COSF25 TMPRSS2_ENST00000332149 1(UTR) 1_79 - ERG_ENST00000442448 4 312_5034 - 492 21.34%
COSF28 TMPRSS2_ENST00000332149 2 1_150 - ERG_ENST00000442448 4 312_5034 - 38 1.65%
COSF23 TMPRSS2_ENST00000332149 1(UTR) 1_79 - ERG_ENST00000442448 2(UTR) 124_5034 - 27 1.17%
COSF26 TMPRSS2_ENST00000332149 1(UTR) 1_79 - ERG_ENST00000442448 5 530_5034 - 21 .91%
COSF27 TMPRSS2_ENST00000332149 2 1_150 - ERG_ENST00000442448 2(UTR) 124_5034 - 7 .3%
COSF736 TMPRSS2_ENST00000332149 2 1_150 - ERG_ENST00000442448 3 226_5034 - 4 .17%
COSF16 TMPRSS2_ENST00000332149 5 1_580 - ERG_ENST00000442448 4 312_5034 - 3 .13%
COSF29 TMPRSS2_ENST00000332149 2 1_150 - ERG_ENST00000442448 5 530_5034 - 3 .13%
COSF30 TMPRSS2_ENST00000332149 3 1_373 - ERG_ENST00000442448 4 312_5034 - 3 .13%
COSF135 TMPRSS2_ENST00000332149 3 1_373 - ERG_ENST00000442448 2(UTR) 124_5034 - 3 .13%
COSF24 TMPRSS2_ENST00000332149 1(UTR) 1_79 - ERG_ENST00000442448 3 226_5034 - 3 .13%
COSF18 TMPRSS2_ENST00000332149 4 1_460 - ERG_ENST00000442448 4 312_5034 - 1 .04%
COSF139 TMPRSS2_ENST00000332149 1(UTR) 1_79+? - ERG_ENST00000442448 4 312_5034 - 1 .04%
COSF21 TMPRSS2_ENST00000332149 ? ? - ERG_ENST00000442448 ? ? - 1700 74%
Total Mutations2306100%

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