BRD3
bromodomain containing 3
Summary
This gene was identified based on its homology to the gene encoding the RING3 protein, a serine/threonine kinase. The gene localizes to 9q34, a region which contains several major histocompatibility complex (MHC) genes. The function of the encoded protein is not known. [provided by RefSeq, Jul 2008]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3180509 | 9:136,897,978 | A/C | — | — |
| rs1340507235 | 9:136,901,265 | A/C | — | uncertain significance |
| rs2539487494 | 9:136,901,325 | C/T | — | uncertain significance |
| rs199538941 | 9:136,901,408 | T/C | — | uncertain significance |
| rs2132392562 | 9:136,905,166 | T/C | — | likely benign |
| rs1183922095 | 9:136,905,240 | T/G | — | uncertain significance |
| rs1406267961 | 9:136,905,241 | T/C | — | uncertain significance |
| rs1331134256 | 9:136,907,000 | G/A | — | uncertain significance |
| rs467387 | 9:136,907,005 | G/T | synonymous variant | — |
| rs139052198 | 9:136,907,025 | C/A | — | uncertain significance |
| rs200014458 | 9:136,907,057 | C/T | — | uncertain significance |
| rs188580122 | 9:136,907,079 | G/A | — | likely benign |
| rs74498766 | 9:136,907,832 | T/A | — | — |
| rs392134 | 9:136,909,008 | G/A | intron variant | — |
| rs455073 | 9:136,909,141 | G/A | — | — |
| rs1830145204 | 9:136,910,481 | C/T | — | uncertain significance |
| rs456207 | 9:136,911,140 | G/A | intron variant | — |
| rs456205 | 9:136,911,146 | G/A | intron variant | — |
| rs460888 | 9:136,913,123 | C/T | — | — |
| rs1322230565 | 9:136,913,243 | C/T | — | uncertain significance |
| rs1446391044 | 9:136,913,371 | T/C | — | uncertain significance |
| rs201862130 | 9:136,913,387 | C/T | — | uncertain significance |
| rs147905022 | 9:136,913,388 | G/A | — | benign |
| rs2539530853 | 9:136,913,435 | T/C | — | uncertain significance |
| rs1321690570 | 9:136,913,471 | T/G | — | uncertain significance |
| rs200946674 | 9:136,913,474 | C/T | — | uncertain significance |
| rs202191407 | 9:136,913,497 | G/A | — | uncertain significance |
| rs201027330 | 9:136,913,503 | G/A | — | uncertain significance |
| rs200384607 | 9:136,915,512 | G/A | — | uncertain significance |
| rs1030324882 | 9:136,915,525 | C/T | — | uncertain significance |
| rs202214693 | 9:136,915,531 | C/T | — | likely benign |
| rs199611088 | 9:136,915,573 | C/A | — | uncertain significance |
| rs2539538854 | 9:136,915,593 | G/A | — | uncertain significance |
| rs200047508 | 9:136,915,594 | C/T | — | uncertain significance |
| rs532421538 | 9:136,915,615 | T/G | — | uncertain significance |
| rs772848697 | 9:136,915,617 | G/A | — | uncertain significance |
| rs2539539221 | 9:136,915,638 | G/A | — | uncertain significance |
| rs147626213 | 9:136,915,666 | G/T | — | uncertain significance |
| rs201506493 | 9:136,915,693 | C/T | — | uncertain significance |
| rs2520100 | 9:136,918,137 | A/T | upstream gene variant | — |
| rs201114126 | 9:136,918,503 | C/G | — | uncertain significance |
| rs200385726 | 9:136,918,553 | G/A | — | uncertain significance |
| rs13297632 | 9:136,918,555 | G/T | — | benign |
| rs201355820 | 9:136,918,571 | G/A | — | uncertain significance |
| rs11789898 | 9:136,925,663 | G/A | — | — |
| rs72766630 | 9:136,926,791 | G/T | downstream gene variant | — |
| rs7027509 | 9:136,927,876 | C/G | — | — |
| rs736903 | 9:136,929,229 | A/G | intron variant | — |
| rs10993908 | 9:136,929,545 | C/T | intron variant | — |
| rs55924785 | 9:136,929,586 | C/T | intron variant | — |
| rs11794274 | 9:136,930,504 | C/G | intron variant | — |
| rs11792729 | 9:136,930,586 | G/A | intron variant | — |
| rs2506715 | 9:136,930,894 | G/A | regulatory region variant | — |
| rs72766638 | 9:136,931,778 | C/A | intron variant | — |
| rs75842226 | 9:136,932,410 | G/A | regulatory region variant | — |
| rs13286757 | 9:136,932,587 | G/C | — | — |
| rs13287061 | 9:136,932,706 | G/T | regulatory region variant | — |
| rs75318400 | 9:136,933,445 | T/C | regulatory region variant | — |
| rs146671954 | 9:136,934,203 | G/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.