GRCh38 · COSMIC v83

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
COSF2324 SET 7 1167 - NUP214 18 2581 - 24 58.54%
COSF2329 SET 7 1167 - NUP214 17 2422 - 2 4.88%
COSF2357 SET 7 1167+174 - NUP214 18 2581-5332 - 1 2.44%
COSF2330 SET 8 2008 - NUP214 18 2581-2219 - 1 2.44%
COSF2331 SET 8 2581 - NUP214 18 2581-752 - 1 2.44%
COSF2326 SET 7 1167+26 y NUP214 18 2581-732 - 1 2.44%
COSF2325 SET 7 1167+261 y NUP214 18 2581-5716 - 1 2.44%
COSF2327 SET 7 1167+430 - NUP214 18 2581-3939 - 1 2.44%
COSF2333 SET ? ? - NUP214 ? ? - 9 22%
Total Mutations41100%

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