GRCh38 · COSMIC v90

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
VTI1A - TCF7L2_ENST00000369397

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
COSF1147 VTI1A 2 1_269 - TCF7L2_ENST00000369397 5 789_3802 - 1 25%
COSF1153 VTI1A 3 1_380 - TCF7L2_ENST00000369397 4 687_3802 - 1 25%
COSF1151 VTI1A 4 1_458 - TCF7L2_ENST00000369397 5 789_3802 - 1 25%
COSF1149 VTI1A 3 1_380 - TCF7L2_ENST00000369397 5 789_3802 - 1 25%
Total Mutations4100%

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