GRCh38 · COSMIC v94

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
COSF1998 KMT2A 8 1_4109 - EPS15 2 131_5225 - 3 23.08%
COSF2000 EPS15 1 1_130 - KMT2A 9 4110_16602 - 2 15.38%
COSF2004 KMT2A 9 1_4145 - EPS15 10 749-344_5225 - 2 15.38%
COSF2006 EPS15 9 1_748+606 - KMT2A 9 4156_16602 - 2 15.38%
COSF2007 KMT2A 10 1_4355 - EPS15 12 1052_5225 - 1 7.69%
COSF2002 KMT2A ? ? - EPS15 ? ? - 3 23%
Total Mutations13100%

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