GRCh38 · COSMIC v83

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
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
COSF1272 CCDC6 1 535 - RET 12 2369 - 585 98.65%
COSF1516 CCDC6 2 685 - RET 12 2369 - 3 .51%
COSF1532 CCDC6 1 535+1111 - RET 12 2369-807 - 1 .17%
COSF1533 CCDC6 1 535+1054 - RET 12 2369-? - 1 .17%
COSF1518 CCDC6 8 1462+848 - RET 11 2237 - 1 .17%
COSF1480 CCDC6 ? ? - RET ? ? - 2 0%
Total Mutations593100%

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