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
CCDC6 - RET

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
COSF1271 CCDC6 1 1_535 - RET 12 2369_5659 - 585 98.65%
COSF1515 CCDC6 2 1_685 - RET 12 2369_5659 - 3 .51%
COSF1532 CCDC6 1 1_535+1111 - RET 12 2369-807_5659 - 1 .17%
COSF1533 CCDC6 1 1_535+1054 - RET 12 2369-?_5659 - 1 .17%
COSF1518 CCDC6 8 1_1462+848 - RET 11 2237_5659 - 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