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
COSF355 EWSR1 12 1613 - NR4A3 3 728 - 28 31.82%
COSF356 EWSR1 7 1112 - NR4A3 1(utr) 554 - 11 12.5%
COSF397 EWSR1 13 1736+340 - NR4A3 3 728-1696 - 2 2.27%
COSF365 EWSR1 12 1543 - NR4A3 3 728 - 1 1.14%
COSF366 EWSR1 12 1543 - NR4A3 3 728-816 - 1 1.14%
COSF369 EWSR1 13 1736 - NR4A3 3 728 - 1 1.14%
COSF370 EWSR1 12 1613+309 y NR4A3 3 728-5 - 1 1.14%
COSF402 NR4A3 2(utr) 727+404 - EWSR1 13 1614-251 - 1 1.14%
COSF374 EWSR1 12 1613+1052 - NR4A3 3 728-1754 - 1 1.14%
COSF375 EWSR1 12 1613+1443 y NR4A3 3 728-1542 - 1 1.14%
COSF378 EWSR1 12 1613+1150 - NR4A3 3 728-286 - 1 1.14%
COSF380 EWSR1 12 1613+647 y NR4A3 3 728-1438 - 1 1.14%
COSF386 NR4A3 2(utr) 727+695 - EWSR1 13 1614-810 - 1 1.14%
COSF398 EWSR1 12 1613+430 - NR4A3 3 728-368 - 1 1.14%
COSF399 EWSR1 7 1112+1373 - NR4A3 2(utr) 554-1631 - 1 1.14%
COSF401 NR4A3 2(utr) 727+655 - EWSR1 13 1632 - 1 1.14%
COSF361 EWSR1 10 1364 - NR4A3 3 728-1311 - 1 1.14%
COSF359 EWSR1 11 1483 - NR4A3 1(utr) 550 - 1 1.14%
COSF400 EWSR1 12 1613+1304 - NR4A3 2(utr) 554-1806 - 1 1.14%
COSF371 EWSR1 12 1613+774 - NR4A3 3 728-1056 - 1 1.14%
COSF496 EWSR1 ? ? - NR4A3 ? ? - 30 34%
Total Mutations88100%

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