GRCh38 · COSMIC v82

Overview

This inferred breakpoint table displays list of all inferred breakpoints derived from expression of number of gene fusion mRNA variants. You can see more information on the help pages.

Genes
PML - RARA

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
COSF2300 PML 6 1753+? - RARA 3 634-? - 314 57.72%
COSF2302 PML 3 1279+? - RARA 3 634-? - 169 31.07%
COSF2305 PML 6 1753 - RARA 3 634-? - 26 4.78%
COSF2316 PML 6 1753+765 - RARA 3 634-2464 - 1 .18%
COSF2317 PML 6 1753+594 - RARA 3 634-4872 - 1 .18%
COSF2320 PML 6 1753 - RARA 3 634-9222 - 1 .18%
COSF2313 PML 6 1753+662 - RARA 3 634-372 - 1 .18%
COSF2322 PML 6 1753 - RARA 3 634-16840 - 1 .18%
COSF2311 PML 5 1494 - RARA 3 634 - 1 .18%
COSF2312 PML 7 1756 - RARA 3 634-647 - 1 .18%
COSF2304 PML ? ? - RARA ? ? - 28 5%
Total Mutations544100%

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