GRCh38 · COSMIC v82

Overview

This inferred breakpoint table displays list of all inferred breakpoints derived from expression of number of 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
COSF2341 NUP214 31 5893 - ABL1 2 461 - 13 28.89%
COSF2343 NUP214 32 6046 - ABL1 2 461 - 7 15.56%
COSF2345 NUP214 34 6358 - ABL1 2 461 - 7 15.56%
COSF2339 NUP214 29 5665 - ABL1 2 461 - 5 11.11%
COSF2359 NUP214 34 6358 - ABL1 3 635 - 4 8.89%
COSF2348 NUP214 31 5893 - ABL1 3 635 - 3 6.67%
COSF2350 NUP214 29 5665 - ABL1 3 635 - 1 2.22%
COSF2352 NUP214 28 3865 - ABL1 2 461 - 1 2.22%
COSF2354 NUP214 32 6046 - ABL1 3 635 - 1 2.22%
COSF2356 NUP214 30 5736 - ABL1 2 461 - 1 2.22%
COSF2337 NUP214 23 3463 - ABL1 2 461 - 1 2.22%
COSF2346 NUP214 ? ? - ABL1 ? ? - 1 2%
Total Mutations45100%

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