GRCh38 · COSMIC v90

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
COSF657 TAF15_ENST00000604841 6 1_556 - NR4A3_ENST00000395097 3 728_3794 - 12 66.67%
COSF961 NR4A3_ENST00000395097 2(UTR) 1_727+1779_insCA y TAF15_ENST00000604841 7 557-113_2140 - 1 5.56%
COSF959 TAF15_ENST00000604841 6 1_556+1130 - NR4A3_ENST00000395097 3 728_3794 - 1 5.56%
COSF960 NR4A3_ENST00000395097 2(UTR) 1_727+877_insG y TAF15_ENST00000604841 7 557-848_2140 - 1 5.56%
COSF957 TAF15_ENST00000604841 6 1_556+42 - NR4A3_ENST00000395097 3 728-811_3794 - 1 5.56%
COSF958 TAF15_ENST00000604841 6 1_556+659 - NR4A3_ENST00000395097 3 728-1113_3794 - 1 5.56%
COSF589 TAF15_ENST00000604841 ? ? - NR4A3_ENST00000395097 ? ? - 1 6%
Total Mutations18100%

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