GRCh38 · COSMIC v87

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
COSF2378 RUNX1 5 1058 - RUNX1T1 2 189 - 397 95.2%
COSF2380 RUNX1 5 1058+1583 - RUNX1T1 2 189-18980 - 1 .24%
COSF2381 RUNX1 5 1058+1701 - RUNX1T1 2 189-? - 1 .24%
COSF2382 RUNX1 5 1058+3310 - RUNX1T1 2 189-47652 - 1 .24%
COSF2383 RUNX1 5 1058+3743 - RUNX1T1 2 189-50292 - 1 .24%
COSF2384 RUNX1 5 1058+5280 - RUNX1T1 2 189-48885 - 1 .24%
COSF2385 RUNX1 5 1058+5833 - RUNX1T1 2 189-48530 - 1 .24%
COSF2386 RUNX1 5 1058+7292 y RUNX1T1 2 189-46268 - 1 .24%
COSF2387 RUNX1 5 1058+9896 - RUNX1T1 2 189-45641 - 1 .24%
COSF2388 RUNX1 5 1058+13018 y RUNX1T1 2 189-47920 - 1 .24%
COSF2389 RUNX1 5 1058+18045 - RUNX1T1 2 189-6156 - 1 .24%
COSF2390 RUNX1 5 1058+20035 y RUNX1T1 2 189-47279 - 1 .24%
COSF2391 RUNX1 5 1058+20556 - RUNX1T1 2 189-50107 - 1 .24%
COSF2392 RUNX1 5 1058+20901 - RUNX1T1 2 189-48605 - 1 .24%
COSF2393 RUNX1 5 1058+21621 - RUNX1T1 2 189-53103 - 1 .24%
COSF2394 RUNX1 5 1058+22317 - RUNX1T1 2 189-53469 - 1 .24%
COSF2395 RUNX1 5 1058+22881 - RUNX1T1 2 189-10446 - 1 .24%
COSF2396 RUNX1 5 1058+23239 y RUNX1T1 2 189-45811 - 1 .24%
COSF2397 RUNX1 5 1058+24393 - RUNX1T1 2 189-36192 - 1 .24%
COSF2398 RUNX1 5 1058+? - RUNX1T1 2 189-? - 1 .24%
COSF2379 RUNX1 5 1058+29 - RUNX1T1 2 189-6649 - 1 .24%
Total Mutations417100%

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