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
COSF999 PCM1 36 6280 - JAK2 11 1821 - 4 22.22%
COSF997 JAK2 10 1820 - PCM1 37 6281 - 2 11.11%
COSF1006 JAK2 11 2007 - PCM1 25 4548 - 1 5.56%
COSF1008 PCM1 26 4849 - JAK2 9 1551 - 1 5.56%
COSF1010 PCM1 36 6280 - JAK2 9 1551 - 1 5.56%
COSF1012 PCM1 36 6280+5205 - JAK2 11 1845 - 1 5.56%
COSF1002 PCM1 23 4382 - JAK2 12 2008 - 1 5.56%
COSF1004 PCM1 24 4547 - JAK2 17 2626 - 1 5.56%
COSF1000 PCM1 ? ? - JAK2 ? ? - 6 33%
Total Mutations18100%

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