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
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
COSF1330 TPM3 7 717 - NTRK1_ENST00000392302 10 1262 - 29 76.32%
COSF1332 NTRK1_ENST00000392302 9 1261 - TPM3 8 718 - 4 10.53%
COSF1320 TPM3 7 717+9360 - NTRK1_ENST00000392302 10 1262-154 - 1 2.63%
COSF1322 NTRK1_ENST00000392302 9 1261+445 - TPM3 8 718-3315 - 1 2.63%
COSF1319 TPM3 7 717+6032 - NTRK1_ENST00000392302 10 1262-84 - 1 2.63%
COSF1318 TPM3 7 717+9871 - NTRK1_ENST00000392302 10 1262-217 - 1 2.63%
COSF1321 NTRK1_ENST00000392302 9 1261+393 - TPM3 8 718-2796 - 1 2.63%
Total Mutations38100%

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