GRCh38 · COSMIC v95

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
COSF1856 KMT2A 10 1_4355 - MLLT3 6 1413_6772 - 20 26.32%
COSF2081 KMT2A 8 1_4109 - MLLT3 6 1413_6772 - 11 14.47%
COSF2083 KMT2A 8 1_4109 - MLLT3 9 1719_6772 - 7 9.21%
COSF2087 KMT2A 10 1_4355 - MLLT3 5 708_6772 - 3 3.95%
COSF2085 KMT2A 8 1_4109 - MLLT3 10 1791_6772 - 2 2.63%
COSF1857 KMT2A 9 1_4241 - MLLT3 6 1413_6772 - 2 2.63%
COSF1984 MLLT3 5 1_1412+12829 - KMT2A 10 4242-188_16602 - 1 1.32%
COSF1983 KMT2A 10 1_4293 - MLLT3 6 1413-35265_6772 - 1 1.32%
COSF1986 KMT2A 7 1_4035+106 - MLLT3 7 1489-270_6772 - 1 1.32%
COSF1861 KMT2A ? ? - MLLT3 ? ? - 28 37%
Total Mutations76100%

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