GRCh38 · COSMIC v95

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
NUP214 - SET_ENST00000322030

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
COSF2323 SET_ENST00000322030 7 1_1167 - NUP214 18 2581_7600 - 26 60.47%
COSF2328 SET_ENST00000322030 7 1_1167 - NUP214 17 2422_7600 - 2 4.65%
COSF2357 SET_ENST00000322030 7 1_1167+174 - NUP214 18 2581-5332_7600 - 1 2.33%
COSF2330 SET_ENST00000322030 8 1_2008 - NUP214 18 2581-2219_7600 - 1 2.33%
COSF2331 SET_ENST00000322030 8 1_2915 - NUP214 18 2581-753_7600 - 1 2.33%
COSF2326 SET_ENST00000322030 7 1_1167+26_insCCCC y NUP214 18 2581-732_7600 - 1 2.33%
COSF2325 SET_ENST00000322030 7 1_1167+261_insCC y NUP214 18 2581-5716_7600 - 1 2.33%
COSF2327 SET_ENST00000322030 7 1_1167+430 - NUP214 18 2581-3939_7600 - 1 2.33%
COSF2333 SET_ENST00000322030 ? ? - NUP214 ? ? - 9 21%
Total Mutations43100%

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