MAML3
mastermind like transcriptional coactivator 3
Summary
Enables transcription coactivator activity. Involved in Notch signaling pathway and positive regulation of transcription by RNA polymerase II. Located in nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761704857 | 4:140,640,660 | G/C | — | uncertain significance |
| rs4863687 | 4:140,678,281 | C/T | intron variant | — |
| rs190870871 | 4:140,704,428 | T/G | intron variant | — |
| rs4863692 | 4:140,764,124 | G/A | — | — |
| rs4863517 | 4:140,773,858 | C/T | regulatory region variant | — |
| rs34236292 | 4:140,786,038 | G/T | regulatory region variant | — |
| rs3106323 | 4:140,786,361 | T/C | intron variant | — |
| rs1531070 | 4:140,795,327 | G/A | intron variant | — |
| rs72712511 | 4:140,804,901 | A/C | intron variant | — |
| rs767651117 | 4:140,810,599 | C/T | — | uncertain significance |
| rs2546225381 | 4:140,810,892 | C/T | — | uncertain significance |
| rs763680452 | 4:140,810,921 | T/C | — | uncertain significance |
| rs1732428304 | 4:140,811,034 | G/A | — | uncertain significance |
| rs756137223 | 4:140,811,146 | T/C | — | uncertain significance |
| rs547610978 | 4:140,811,265 | G/A | — | uncertain significance |
| rs200939015 | 4:140,811,292 | C/T | — | uncertain significance |
| rs541652595 | 4:140,811,311 | G/A | — | uncertain significance |
| rs1181328351 | 4:140,811,319 | G/C | — | uncertain significance |
| rs751507608 | 4:140,811,386 | C/T | — | uncertain significance |
| rs765267001 | 4:140,811,419 | C/T | — | uncertain significance |
| rs200202141 | 4:140,811,451 | G/A | — | uncertain significance |
| rs368276039 | 4:140,811,737 | T/C | — | uncertain significance |
| rs760036447 | 4:140,811,826 | G/T | — | uncertain significance |
| rs376616820 | 4:140,812,012 | C/A | — | uncertain significance |
| rs762219049 | 4:140,812,039 | T/G | — | uncertain significance |
| rs536058444 | 4:140,812,109 | C/T | — | uncertain significance |
| rs1399683554 | 4:140,812,111 | G/A | — | uncertain significance |
| rs57800857 | 4:140,863,365 | A/T | — | — |
| rs6830759 | 4:140,865,267 | A/C | — | — |
| rs769658 | 4:140,872,682 | C/T | intron variant | — |
| rs3106209 | 4:140,884,723 | A/C | intron variant | — |
| rs13109980 | 4:140,886,963 | G/A | intron variant | — |
| rs56218782 | 4:140,893,287 | T/C | intron variant | — |
| rs35654250 | 4:140,896,461 | C/T | intron variant | — |
| rs35319653 | 4:140,903,155 | C/T | intron variant | — |
| rs12505942 | 4:140,906,390 | T/C | intron variant | — |
| rs35612722 | 4:140,909,431 | G/A | intron variant | — |
| rs13134500 | 4:140,911,732 | A/G | intron variant | — |
| rs13148756 | 4:140,915,940 | G/T | — | — |
| rs6536630 | 4:140,919,035 | T/A | intron variant | — |
| rs17373738 | 4:140,935,264 | C/G | intron variant | — |
| rs36072649 | 4:140,939,110 | T/A | intron variant | — |
| rs56166763 | 4:140,943,169 | G/C | intron variant | — |
| rs55669488 | 4:140,943,275 | T/A | intron variant | — |
| rs17314804 | 4:140,946,828 | C/T | intron variant | — |
| rs911698938 | 4:141,074,129 | A/G | — | uncertain significance |
| rs759366309 | 4:141,074,151 | C/A | — | uncertain significance |
| rs747464661 | 4:141,074,204 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.