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
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
COSF571 ETV6 5 1_1283 - NTRK3_ENST00000394480 15 1908_19984 - 118 81.38%
COSF1534 ETV6 4 1_737 - NTRK3_ENST00000394480 14 1719_19984 - 15 10.34%
COSF1536 ETV6 5 1_1283 - NTRK3_ENST00000394480 14 1719_19984 - 1 .69%
COSF823 ETV6 4 1_737 - NTRK3_ENST00000394480 15 1908_19984 - 1 .69%
COSF825 NTRK3_ENST00000394480 14 1_1907 - ETV6 6 1284_5989 - 1 .69%
COSF495 ETV6 ? ? - NTRK3_ENST00000394480 ? ? - 9 6%
Total Mutations145100%

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