GRCh38 · COSMIC v99

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
COSF198 NPM1_ENST00000517671 5 1_487 - ALK 20 4080_6220 - 302 94.67%
COSF449 NPM1_ENST00000517671 5 1_487+201 - ALK 20 4080-24_6220 - 1 .31%
COSF450 NPM1_ENST00000517671 5 1_487+230 - ALK 20 4080-1134_6220 - 1 .31%
COSF451 NPM1_ENST00000517671 5 1_487+295 - ALK 20 4080-954_6220 - 1 .31%
COSF458 NPM1_ENST00000517671 5 1_487+897 - ALK 20 4080-1511_6220 - 1 .31%
COSF453 NPM1_ENST00000517671 5 1_487+443 - ALK 20 4080-1040_6220 - 1 .31%
COSF454 NPM1_ENST00000517671 5 1_487+546 - ALK 20 4080-583_6220 - 1 .31%
COSF455 NPM1_ENST00000517671 5 1_487+726 - ALK 20 4080-660_6220 - 1 .31%
COSF456 NPM1_ENST00000517671 5 1_487+778 - ALK 20 4080-208_6220 - 1 .31%
COSF457 NPM1_ENST00000517671 5 1_487+865 - ALK 20 4080-629_6220 - 1 .31%
COSF448 NPM1_ENST00000517671 5 1_487+192 - ALK 20 4080-616_6220 - 1 .31%
COSF452 NPM1_ENST00000517671 5 1_487+358 - ALK 20 4080-1128_6220 - 1 .31%
COSF420 NPM1_ENST00000517671 ? ? - ALK ? ? - 6 2%
Total Mutations319100%

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