GRCh38 · COSMIC v98

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
ACTB - GLI1

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
COSF1384 ACTB 3 1_555 - GLI1 5 562_3613 - 1 12.5%
COSF1389 ACTB 3 1_555+134 - GLI1 7 771_3613 - 1 12.5%
COSF1390 GLI1 7 1_722 - ACTB 4 556-24_1921 - 1 12.5%
COSF1391 ACTB 1(UTR) 1_186+817 - GLI1 6 626-1_3613 - 1 12.5%
COSF1395 GLI1 5 1_625+49 - ACTB 4 556-390_1921 - 1 12.5%
COSF1393 ACTB 2 1_315+119 - GLI1 6 626-202_3613 - 1 12.5%
COSF1394 ACTB 3 1_555+5 - ACTB 3 416_674inv::ENST00000228682.6(GLI1):r.626-349_3613 - 1 12.5%
COSF1394 ACTB 3 1_555+5 - GLI1 6 416_674inv::ENST00000228682.6(GLI1):r.626-349_3613 - 1 12.5%
COSF1392 ACTB 3 1_555+238 - GLI1 7 716-34_3613 - 1 12.5%
Total Mutations8100%

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