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
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
COSF1489 TCF3 16 1_1519 - PBX1 3 454_6636 - 271 90.03%
COSF2123 TCF3 16 1_1519_ins27 y PBX1 3 454_6636 - 5 1.66%
COSF2130 TCF3 16 1_1519+1178_insTT y PBX1 3 454-8164_6636 - 2 .66%
COSF2134 TCF3 16 1_1519+1180_ins15 y PBX1 3 454-90188_6636 - 2 .66%
COSF2128 TCF3 16 1_1519+1176_insTCCA y PBX1 3 454-6432_6636 - 1 .33%
COSF2129 TCF3 16 1_1519+1178_insCGCTCCT y PBX1 3 454-97674_6636 - 1 .33%
COSF2131 TCF3 16 1_1519+1179_ins15 y PBX1 3 454-5970_6636 - 1 .33%
COSF2132 TCF3 16 1_1519+1180_ins13 y PBX1 3 454-9547_6636 - 1 .33%
COSF2133 TCF3 16 1_1519+1180_ins18 y PBX1 3 454-1682_6636 - 1 .33%
COSF2135 TCF3 16 1_1519+1182_ins11 y PBX1 3 454-9148_6636 - 1 .33%
COSF2136 TCF3 16 1_1519+1182_ins15 y PBX1 3 454-5205_6636 - 1 .33%
COSF2137 TCF3 16 1_1519+1182_ins39 y PBX1 3 454-88161_6636 - 1 .33%
COSF2138 TCF3 16 1_1519+1183_ins41 y PBX1 3 454-31181_6636 - 1 .33%
COSF2140 TCF3 16 1_1519+1183_ins13 y PBX1 3 454-42744_6636 - 1 .33%
COSF2141 TCF3 16 1_1519+1183_insAG y PBX1 3 454-17910_6636 - 1 .33%
COSF2142 TCF3 16 1_1519+1183_ins16 y PBX1 3 454-2420_6636 - 1 .33%
COSF2143 TCF3 16 1_1519+1183_insTGGAGTCCG y PBX1 3 454-6267_6636 - 1 .33%
COSF2144 TCF3 16 1_1519+2081_ins49 y PBX1 3 454-96292_6636 - 1 .33%
COSF2145 TCF3 16 1_1519+2352_ins17 y PBX1 3 454-106920_6636 - 1 .33%
COSF2146 TCF3 16 1_1519+3096 - PBX1 3 454-101357_6636 - 1 .33%
COSF2127 TCF3 16 1_1519+1171_insAACTGA y PBX1 3 454-43111_6636 - 1 .33%
COSF2126 TCF3 16 1_1519+933_insAGGCTC y PBX1 3 454-1406_6636 - 1 .33%
COSF2125 TCF3 16 1_1519+584_ins19 y PBX1 3 454-108174_6636 - 1 .33%
COSF2147 TCF3 16 1_1519+3099_insGGCC y PBX1 3 454-86772_6636 - 1 .33%
COSF2121 TCF3 17 1_1655 - PBX1 5 890_6636 - 1 .33%
Total Mutations301100%

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