GRCh38 · COSMIC v90

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
COSF352 EWSR1_ENST00000397938 12 1_1613 - NR4A3_ENST00000395097 3 728_3794 - 28 31.82%
COSF353 EWSR1_ENST00000397938 7 1_1112 - NR4A3_ENST00000395097 1(UTR) 1_3794 - 11 12.5%
COSF397 EWSR1_ENST00000397938 13 1_1736+340 - NR4A3_ENST00000395097 3 728-1696_3794 - 2 2.27%
COSF364 EWSR1_ENST00000397938 12 1_1543 - NR4A3_ENST00000395097 3 728_3794 - 1 1.14%
COSF366 EWSR1_ENST00000397938 12 1_1543 - NR4A3_ENST00000395097 3 728-816_3794 - 1 1.14%
COSF367 EWSR1_ENST00000397938 13 1_1736 - NR4A3_ENST00000395097 3 728_3794 - 1 1.14%
COSF370 EWSR1_ENST00000397938 12 1_1613+309_insACCTTTTCTCTTGTCCCCTA y NR4A3_ENST00000395097 3 728-5_3794 - 1 1.14%
COSF402 NR4A3_ENST00000395097 2(UTR) 1_727+404 - EWSR1_ENST00000397938 13 1614-251_2654 - 1 1.14%
COSF374 EWSR1_ENST00000397938 12 1_1613+1052 - NR4A3_ENST00000395097 3 728-1754_3794 - 1 1.14%
COSF375 EWSR1_ENST00000397938 12 1_1613+1443_insTGTT y NR4A3_ENST00000395097 3 728-1542_3794 - 1 1.14%
COSF378 EWSR1_ENST00000397938 12 1_1613+1150 - NR4A3_ENST00000395097 3 728-286_3794 - 1 1.14%
COSF380 EWSR1_ENST00000397938 12 1_1613+647_insG y NR4A3_ENST00000395097 3 728-1438_3794 - 1 1.14%
COSF386 NR4A3_ENST00000395097 2(UTR) 1_727+695 - EWSR1_ENST00000397938 13 1614-810_2654 - 1 1.14%
COSF398 EWSR1_ENST00000397938 12 1_1613+430 - NR4A3_ENST00000395097 3 728-368_3794 - 1 1.14%
COSF399 EWSR1_ENST00000397938 7 1_1112+1373 - NR4A3_ENST00000395097 2(UTR) 554-1631_3794 - 1 1.14%
COSF401 NR4A3_ENST00000395097 2(UTR) 1_727+655 - EWSR1_ENST00000397938 13 1632_2654 - 1 1.14%
COSF361 EWSR1_ENST00000397938 10 1_1364 - NR4A3_ENST00000395097 3 728-1311_3794 - 1 1.14%
COSF359 EWSR1_ENST00000397938 11 1_1483 - NR4A3_ENST00000395097 1(UTR) 1_3794 - 1 1.14%
COSF400 EWSR1_ENST00000397938 12 1_1613+1304 - NR4A3_ENST00000395097 2(UTR) 554-1806_3794 - 1 1.14%
COSF371 EWSR1_ENST00000397938 12 1_1613+774 - NR4A3_ENST00000395097 3 728-1056_3794 - 1 1.14%
COSF496 EWSR1_ENST00000397938 ? ? - NR4A3_ENST00000395097 ? ? - 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