BCL9
BCL9 transcription coactivator
Summary
BCL9 is associated with B-cell acute lymphoblastic leukemia. It may be a target of translocation in B-cell malignancies with abnormalities of 1q21. Its function is unknown. The overexpression of BCL9 may be of pathogenic significance in B-cell malignancies. [provided by RefSeq, Jul 2008]
Known Variants100 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs587615347 | 1:147,017,126 | C/T | — | — |
| rs594206 | 1:147,020,456 | A/G | intron variant | — |
| rs9326555 | 1:147,022,306 | C/G | intron variant | — |
| rs12118839 | 1:147,078,598 | G/C | — | — |
| rs583583 | 1:147,083,114 | C/T | regulatory region variant | — |
| rs41299583 | 1:147,083,650 | C/T | — | likely benign |
| rs782240143 | 1:147,084,714 | G/A | — | uncertain significance |
| rs782339120 | 1:147,084,745 | C/G | — | uncertain significance |
| rs762060274 | 1:147,084,761 | A/G | — | uncertain significance |
| rs41295833 | 1:147,084,965 | C/T | — | likely benign |
| rs147379432 | 1:147,086,288 | C/T | — | uncertain significance |
| rs587660666 | 1:147,086,294 | A/T | — | uncertain significance |
| rs1178128117 | 1:147,086,306 | C/A | — | uncertain significance |
| rs369834661 | 1:147,086,322 | C/A | — | uncertain significance |
| rs782599827 | 1:147,087,643 | G/A | — | uncertain significance |
| rs375569438 | 1:147,087,684 | G/C | — | uncertain significance |
| rs201382423 | 1:147,090,614 | G/T | — | likely benign |
| rs149004972 | 1:147,090,647 | A/G | — | conflicting classifications of pathogenicity |
| rs1553204279 | 1:147,090,669 | A/C | — | uncertain significance |
| rs782766696 | 1:147,090,679 | G/A | — | uncertain significance |
| rs2526648976 | 1:147,090,728 | C/T | — | uncertain significance |
| rs373639033 | 1:147,090,743 | C/T | — | uncertain significance |
| rs782092791 | 1:147,090,773 | C/T | — | uncertain significance |
| rs143556015 | 1:147,090,775 | C/T | — | uncertain significance |
| rs142428017 | 1:147,090,866 | G/A | — | conflicting classifications of pathogenicity |
| rs61751616 | 1:147,090,956 | T/C | — | benign |
| rs151299743 | 1:147,091,108 | G/A | — | conflicting classifications of pathogenicity |
| rs587757712 | 1:147,091,124 | C/T | — | uncertain significance |
| rs781871288 | 1:147,091,165 | C/A | — | uncertain significance |
| rs1318865385 | 1:147,091,354 | A/G | — | uncertain significance |
| rs147571927 | 1:147,091,393 | G/C | — | uncertain significance |
| rs80312516 | 1:147,091,416 | G/A | — | benign |
| rs1054557337 | 1:147,091,490 | T/C | — | uncertain significance |
| rs146055055 | 1:147,091,507 | C/G | — | uncertain significance |
| rs2526653156 | 1:147,091,511 | C/T | — | uncertain significance |
| rs782581434 | 1:147,091,525 | C/G | — | uncertain significance |
| rs369189038 | 1:147,091,643 | G/A | — | uncertain significance |
| rs2526653827 | 1:147,091,648 | C/G | — | uncertain significance |
| rs2526653833 | 1:147,091,649 | C/A | — | uncertain significance |
| rs150675055 | 1:147,091,671 | C/A | — | uncertain significance |
| rs782454130 | 1:147,091,708 | T/C | — | uncertain significance |
| rs189581138 | 1:147,091,888 | C/A | — | uncertain significance |
| rs138790542 | 1:147,091,925 | G/A | — | uncertain significance |
| rs376171487 | 1:147,091,927 | A/T | — | uncertain significance |
| rs1658537778 | 1:147,091,951 | G/T | — | uncertain significance |
| rs782700818 | 1:147,091,961 | G/A | — | uncertain significance |
| rs3820129 | 1:147,091,972 | C/G | missense variant | — |
| rs782218422 | 1:147,091,997 | G/A | — | uncertain significance |
| rs959447674 | 1:147,092,002 | C/G | — | uncertain significance |
| rs2526656116 | 1:147,092,047 | G/A | — | uncertain significance |
| rs2526656206 | 1:147,092,065 | G/T | — | uncertain significance |
| rs372034307 | 1:147,092,095 | G/A | — | uncertain significance |
| rs375152056 | 1:147,092,120 | T/G | — | uncertain significance |
| rs782735343 | 1:147,092,143 | T/G | — | uncertain significance |
| rs369375635 | 1:147,092,186 | C/T | — | uncertain significance |
| rs375997146 | 1:147,092,213 | G/C | — | uncertain significance |
| rs2526657031 | 1:147,092,249 | A/T | — | uncertain significance |
| rs369043753 | 1:147,092,259 | A/G | — | likely benign |
| rs782819434 | 1:147,092,284 | C/G | — | uncertain significance |
| rs2526657291 | 1:147,092,320 | A/G | — | uncertain significance |
| rs782572053 | 1:147,092,323 | T/G | — | uncertain significance |
| rs782707705 | 1:147,092,354 | G/A | — | uncertain significance |
| rs781867942 | 1:147,092,357 | A/C | — | uncertain significance |
| rs781931002 | 1:147,092,476 | C/T | — | uncertain significance |
| rs782102524 | 1:147,092,594 | C/T | — | uncertain significance |
| rs781869325 | 1:147,092,600 | C/T | — | uncertain significance |
| rs140389189 | 1:147,092,648 | T/C | — | uncertain significance |
| rs782041474 | 1:147,092,674 | A/G | — | uncertain significance |
| rs919637786 | 1:147,092,737 | C/T | — | uncertain significance |
| rs1490457473 | 1:147,094,081 | C/A | — | uncertain significance |
| rs200473630 | 1:147,094,140 | A/G | — | uncertain significance |
| rs781943517 | 1:147,094,248 | G/T | — | uncertain significance |
| rs1045720124 | 1:147,094,293 | G/A | — | uncertain significance |
| rs377334839 | 1:147,094,306 | A/C | — | uncertain significance |
| rs781962838 | 1:147,095,667 | C/A | — | uncertain significance |
| rs373321043 | 1:147,095,669 | C/T | — | uncertain significance |
| rs587670636 | 1:147,095,670 | G/A | — | uncertain significance |
| rs2526672967 | 1:147,095,688 | C/G | — | uncertain significance |
| rs142647046 | 1:147,095,727 | C/A | — | uncertain significance |
| rs1332590475 | 1:147,095,766 | A/G | — | uncertain significance |
| rs199772833 | 1:147,095,792 | C/T | — | uncertain significance |
| rs1658796622 | 1:147,095,801 | C/T | — | uncertain significance |
| rs1198547354 | 1:147,095,831 | C/A | — | uncertain significance |
| rs149196080 | 1:147,095,862 | C/T | — | uncertain significance |
| rs148371186 | 1:147,095,875 | A/G | — | likely benign |
| rs782777168 | 1:147,095,952 | C/T | — | uncertain significance |
| rs139128167 | 1:147,095,976 | C/T | — | uncertain significance |
| rs116866277 | 1:147,096,026 | C/G | — | uncertain significance |
| rs781896625 | 1:147,096,048 | C/T | — | uncertain significance |
| rs113081863 | 1:147,096,153 | G/A | — | benign |
| rs1553206094 | 1:147,096,171 | T/C | — | uncertain significance |
| rs138508726 | 1:147,096,222 | C/T | — | uncertain significance |
| rs375821703 | 1:147,096,248 | G/A | — | uncertain significance |
| rs782114512 | 1:147,096,257 | C/A | — | uncertain significance |
| rs141699147 | 1:147,096,378 | C/T | — | uncertain significance |
| rs1553206203 | 1:147,096,486 | C/T | — | uncertain significance |
| rs200238676 | 1:147,096,500 | A/G | — | uncertain significance |
| rs782163147 | 1:147,096,506 | G/A | — | uncertain significance |
| rs782798002 | 1:147,096,654 | A/G | — | uncertain significance |
| rs150292509 | 1:147,096,672 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.