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
COSF1352 FGFR3 17 2530+38 - TACC3 11 2048-1459 - 2 14.29%
COSF1435 FGFR3 17 2530 - TACC3 10 1943 - 2 14.29%
COSF1354 FGFR3 18 2654 - TACC3 8 1751-371 - 1 7.14%
COSF1356 FGFR3 17 2530+136 - TACC3 11 2048-1830 - 1 7.14%
COSF1358 FGFR3 17 2530+63 - TACC3 9 1877 - 1 7.14%
COSF1360 FGFR3 17 2530 - TACC3 10 1943 - 1 7.14%
COSF1351 FGFR3 17 2530+104 - TACC3 4 541 - 1 7.14%
COSF1349 FGFR3 17 2530+27 - TACC3 11 2048-1511 - 1 7.14%
COSF1355 FGFR3 17 2530 - TACC3 8 1751 - 1 7.14%
COSF1361 FGFR3 ? ? - TACC3 ? ? - 3 21%
Total Mutations14100%

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