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
COSF1492 NCOA4_ENST00000452682 8 1014 - RET 12 2369 - 351 97.23%
COSF1341 NCOA4_ENST00000452682 7 870+196 - RET 12 2369-1570 - 3 .83%
COSF1531 NCOA4_ENST00000452682 8 1014+21 - RET 12 2369-1591 - 1 .28%
COSF1499 NCOA4_ENST00000452682 8 996 - RET 12 2369-? - 1 .28%
COSF1501 NCOA4_ENST00000452682 8 1014+1186 - RET 11 2273 - 1 .28%
COSF1502 RET 11 2271 - NCOA4_ENST00000452682 9 1015-490 - 1 .28%
COSF1495 RET 11 2368+? - NCOA4_ENST00000452682 8 871-? - 1 .28%
COSF1493 NCOA4_ENST00000452682 7 870+42 - RET 12 2369-1673 - 1 .28%
COSF1497 RET 11 2368+? - NCOA4_ENST00000452682 9 1015 - 1 .28%
Total Mutations361100%

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