BRPF3
bromodomain and PHD finger containing 3
Summary
Contributes to histone acetyltransferase activity. Involved in positive regulation of DNA replication. Located in nucleus. Part of MOZ/MORF histone acetyltransferase complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants71 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs748953638 | 6:36,168,116 | G/A | — | uncertain significance |
| rs778397237 | 6:36,168,125 | G/A | — | uncertain significance |
| rs199876915 | 6:36,168,158 | C/T | — | uncertain significance |
| rs763603141 | 6:36,168,251 | G/A | — | uncertain significance |
| rs146114078 | 6:36,168,393 | A/T | — | uncertain significance |
| rs537929575 | 6:36,168,553 | G/A | — | uncertain significance |
| rs372614303 | 6:36,168,597 | G/A | — | uncertain significance |
| rs756136144 | 6:36,168,605 | A/G | — | uncertain significance |
| rs776133125 | 6:36,168,661 | G/A | — | uncertain significance |
| rs200981567 | 6:36,168,668 | G/A | — | uncertain significance |
| rs769122940 | 6:36,168,698 | G/A | — | uncertain significance |
| rs752366945 | 6:36,168,776 | G/A | — | uncertain significance |
| rs80057584 | 6:36,168,835 | G/A | — | uncertain significance |
| rs200164696 | 6:36,168,920 | A/G | — | uncertain significance |
| rs146987553 | 6:36,168,946 | A/G | — | uncertain significance |
| rs1430393594 | 6:36,169,054 | G/A | — | uncertain significance |
| rs2533002961 | 6:36,169,204 | A/T | — | uncertain significance |
| rs775060976 | 6:36,169,253 | C/A | — | uncertain significance |
| rs369791645 | 6:36,169,391 | A/G | — | uncertain significance |
| rs140145706 | 6:36,169,444 | A/C | — | uncertain significance |
| rs754535785 | 6:36,169,495 | G/C | — | uncertain significance |
| rs748148054 | 6:36,169,501 | C/A | — | uncertain significance |
| rs775892441 | 6:36,169,513 | C/T | — | uncertain significance |
| rs777000359 | 6:36,172,527 | G/A | — | uncertain significance |
| rs2533013223 | 6:36,172,538 | C/G | — | uncertain significance |
| rs757375083 | 6:36,175,127 | A/T | — | uncertain significance |
| rs759287564 | 6:36,175,214 | G/A | — | uncertain significance |
| rs143430646 | 6:36,176,689 | G/A | intron variant | — |
| rs1169464362 | 6:36,178,014 | A/G | — | uncertain significance |
| rs199766480 | 6:36,178,048 | G/A | — | uncertain significance |
| rs267600998 | 6:36,178,060 | C/T | — | uncertain significance |
| rs139489461 | 6:36,178,071 | C/T | — | uncertain significance |
| rs2533028803 | 6:36,178,104 | C/T | — | uncertain significance |
| rs767000902 | 6:36,178,156 | G/A | — | uncertain significance |
| rs372943418 | 6:36,178,180 | T/C | — | uncertain significance |
| rs2533029021 | 6:36,178,185 | G/A | — | uncertain significance |
| rs750145294 | 6:36,178,203 | G/A | — | uncertain significance |
| rs759242365 | 6:36,179,182 | A/G | — | uncertain significance |
| rs200449427 | 6:36,179,217 | C/T | — | uncertain significance |
| rs151275478 | 6:36,179,287 | C/G | — | uncertain significance |
| rs547268435 | 6:36,180,300 | G/C | — | — |
| rs774027017 | 6:36,181,678 | C/T | — | uncertain significance |
| rs189565638 | 6:36,181,695 | A/C | — | uncertain significance |
| rs763186938 | 6:36,181,729 | C/T | — | uncertain significance |
| rs767622176 | 6:36,181,734 | C/A | — | uncertain significance |
| rs780304054 | 6:36,181,738 | A/G | — | uncertain significance |
| rs374697575 | 6:36,181,923 | G/A | — | uncertain significance |
| rs368004211 | 6:36,182,012 | G/T | — | uncertain significance |
| rs756837870 | 6:36,182,056 | C/A | — | uncertain significance |
| rs749165206 | 6:36,182,082 | C/T | — | uncertain significance |
| rs769975719 | 6:36,182,127 | G/A | — | uncertain significance |
| rs201068091 | 6:36,185,694 | G/C | — | uncertain significance |
| rs765132054 | 6:36,185,723 | G/A | — | uncertain significance |
| rs145016452 | 6:36,185,759 | A/G | — | likely benign |
| rs749367582 | 6:36,185,781 | C/T | — | uncertain significance |
| rs562718902 | 6:36,190,010 | G/A | — | uncertain significance |
| rs2533058709 | 6:36,190,019 | G/A | — | uncertain significance |
| rs771306997 | 6:36,190,033 | A/G | — | uncertain significance |
| rs532860522 | 6:36,190,034 | A/G | — | likely benign |
| rs149225486 | 6:36,192,232 | G/T | intron variant | — |
| rs140562388 | 6:36,193,076 | G/A | — | uncertain significance |
| rs1414662089 | 6:36,193,115 | C/G | — | uncertain significance |
| rs775759948 | 6:36,196,679 | A/G | — | uncertain significance |
| rs764095322 | 6:36,196,685 | G/A | — | uncertain significance |
| rs780499788 | 6:36,196,719 | A/G | — | uncertain significance |
| rs1437335054 | 6:36,196,743 | C/T | — | uncertain significance |
| rs1332795337 | 6:36,196,776 | A/G | — | uncertain significance |
| rs774699206 | 6:36,198,252 | G/A | — | uncertain significance |
| rs1375658035 | 6:36,198,288 | A/G | — | uncertain significance |
| rs1183660993 | 6:36,198,329 | G/T | — | uncertain significance |
| rs901467824 | 6:36,198,331 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.