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
COSF1806 KMT2A 8 1_4109 - AFDN_ENST00000392108 2 248_6812 - 12 44.44%
COSF2009 KMT2A 9 1_4241 - AFDN_ENST00000392108 2 248_6812 - 6 22.22%
COSF1826 KMT2A 8 1_4109+68 - AFDN_ENST00000392108 2 248-28305_6812 - 1 3.7%
COSF2013 KMT2A 8 1_4109+1026 - AFDN_ENST00000392108 2 248-36549_6812 - 1 3.7%
COSF1810 KMT2A 20 1_5687 - AFDN_ENST00000392108 2 248_6812 - 1 3.7%
COSF1812 KMT2A 22 1_5984+110 - AFDN_ENST00000392108 2 248-1453_6812 - 1 3.7%
COSF2012 KMT2A ? ? - AFDN_ENST00000392108 ? ? - 5 19%
Total Mutations27100%

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