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
BCR - ABL1_ENST00000318560

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
COSF1755 BCR 14 1_3533 - ABL1_ENST00000318560 2 461_5766 - 2886 52.64%
COSF1757 BCR 13 1_3458 - ABL1_ENST00000318560 2 461_5766 - 1792 32.68%
COSF1759 BCR 1 1_2030 - ABL1_ENST00000318560 2 461_5766 - 195 3.56%
COSF1761 BCR 19 1_4073 - ABL1_ENST00000318560 2 461_5766 - 84 1.53%
COSF1743 BCR 14 1_3533 - ABL1_ENST00000318560 3 635_5766 - 16 .29%
COSF1753 BCR 1 1_2030 - ABL1_ENST00000318560 3 635_5766 - 10 .18%
COSF1763 BCR 13 1_3458 - ABL1_ENST00000318560 3 635_5766 - 7 .13%
COSF1794 BCR 8 1_2866 - ABL1_ENST00000318560 2 461-16_5766 - 4 .07%
COSF1774 BCR 13 1_3458+89 - ABL1_ENST00000318560 2 461-4396_5766 - 3 .05%
COSF1751 BCR 6 1_2672 - ABL1_ENST00000318560 2 461_5766 - 3 .05%
COSF1778 BCR 15 1_3631 - ABL1_ENST00000318560 1 1_5766 - 2 .04%
COSF1745 BCR 2 1_2127_insC y ABL1_ENST00000318560 1 388_5766 - 2 .04%
COSF1789 BCR 19 1_4073+82_ins472 y ABL1_ENST00000318560 2 461-416_5766 - 1 .02%
COSF1782 BCR 3 1_2317 - ABL1_ENST00000318560 2 461-?_5766 - 1 .02%
COSF1780 BCR 2 1_2212_insACTAAAGCG y ABL1_ENST00000318560 2 461_5766 - 1 .02%
COSF1773 BCR 8 1_2866 - ABL1_ENST00000318560 2 461-?_5766 - 1 .02%
COSF1769 BCR 19 1_4073+1044 - ABL1_ENST00000318560 2 461-?_5766 - 1 .02%
COSF1768 BCR 13 1_3458+30 - ABL1_ENST00000318560 3 635-517_5766 - 1 .02%
COSF1766 BCR 19 1_4073 - ABL1_ENST00000318560 1 1_5766 - 1 .02%
COSF1748 BCR 13 1_3458_insCTGGATCCATCG y ABL1_ENST00000318560 2 461_5766 - 1 .02%
COSF1740 BCR 8 1_2866 - ABL1_ENST00000318560 2 461_5766 - 1 .02%
COSF1742 BCR 13 1_3410 - ABL1_ENST00000318560 2 461-?_5766 - 1 .02%
COSF1783 BCR ? ? - ABL1_ENST00000318560 ? ? - 469 9%
Total Mutations5483100%

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