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
COSF998 PCM1 36 1_6280 - JAK2 11 1821_5285 - 4 22.22%
COSF996 JAK2 10 1_1820 - PCM1 37 6281_6820 - 2 11.11%
COSF1005 JAK2 11 1_2007 - PCM1 25 4548_6820 - 1 5.56%
COSF1007 PCM1 26 1_4849 - JAK2 9 1551_5285 - 1 5.56%
COSF1009 PCM1 36 1_6280 - JAK2 9 1551_5285 - 1 5.56%
COSF1012 PCM1 36 1_6280+5205 - JAK2 11 1845_5285 - 1 5.56%
COSF1001 PCM1 23 1_4382 - JAK2 12 2008_5285 - 1 5.56%
COSF1003 PCM1 24 1_4547 - JAK2 17 2626_5285 - 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