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
KMT2A - KNL1

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
COSF1870 KMT2A 8 1_4109+1207 - KNL1 11 1648_9573 - 1 16.67%
COSF1871 KMT2A 8 1_4109 - KNL1 12 5845-?_9573 - 1 16.67%
COSF1943 KMT2A 10 1_4277 - KNL1 11 5713_9573 - 1 16.67%
COSF1880 KMT2A 8 1_4109+? - KNL1 11 1324_9573 - 1 16.67%
COSF1881 KMT2A 8 1_4109+? - KNL1 11 3759_9573 - 1 16.67%
COSF1879 KMT2A 9 1_4241+? - KNL1 11 4420_9573 - 1 16.67%
Total Mutations6100%

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