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
COSF1937 KMT2A 8 1_4109+750_insTTAGN y ARHGAP26 12 1493-1280_9395 - 1 33.33%
COSF1940 KMT2A 10 1_4355+90 - ARHGAP26 19 4355+61_4355+1273inv_ENST00000274498.9(ARHGAP26):r.2084-8185_9395 - 1 33.33%
COSF1940 KMT2A 10 1_4355+90 - KMT2A 10 4355+61_4355+1273inv_ENST00000274498.9(ARHGAP26):r.2084-8185_9395 - 1 33.33%
COSF1939 KMT2A 9 1_4241+9_insACACTC y ARHGAP26 19 2084-12703_9395 - 1 33.33%
Total Mutations3100%

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