TASOR
transcription activation suppressor
Summary
Enables chromatin binding activity. Involved in protein localization to heterochromatin and transposable element silencing by heterochromatin formation. Located in heterochromatin and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201657342 | 3:56,658,517 | C/G | — | uncertain significance |
| rs2076757649 | 3:56,658,581 | A/G | — | uncertain significance |
| rs145666615 | 3:56,658,614 | G/A | — | uncertain significance |
| rs767499232 | 3:56,658,618 | T/C | — | uncertain significance |
| rs746181105 | 3:56,658,951 | T/C | — | uncertain significance |
| rs199831929 | 3:56,661,161 | T/A | — | uncertain significance |
| rs1340274922 | 3:56,661,636 | A/G | — | uncertain significance |
| rs1211365635 | 3:56,661,649 | A/G | — | uncertain significance |
| rs778365681 | 3:56,661,673 | A/G | — | uncertain significance |
| rs2472154963 | 3:56,661,685 | A/G | — | uncertain significance |
| rs1170778787 | 3:56,661,745 | T/G | — | uncertain significance |
| rs576098344 | 3:56,662,612 | A/G | — | uncertain significance |
| rs145945392 | 3:56,664,964 | C/G | — | — |
| rs57800049 | 3:56,665,015 | A/T | intron variant | — |
| rs201470008 | 3:56,667,274 | A/G | — | likely benign |
| rs369681222 | 3:56,667,289 | A/G | — | likely benign |
| rs1405580057 | 3:56,667,403 | C/T | — | uncertain significance |
| rs1390921456 | 3:56,667,464 | G/A | — | uncertain significance |
| rs779810934 | 3:56,667,517 | G/A | — | uncertain significance |
| rs200064504 | 3:56,667,593 | C/T | — | uncertain significance |
| rs764600047 | 3:56,667,632 | C/T | — | uncertain significance |
| rs9835332 | 3:56,667,682 | G/A | missense variant | — |
| rs765376721 | 3:56,667,689 | C/T | — | uncertain significance |
| rs139767461 | 3:56,667,725 | T/C | — | uncertain significance |
| rs142269531 | 3:56,667,776 | C/T | — | uncertain significance |
| rs534030408 | 3:56,667,853 | G/C | — | uncertain significance |
| rs1396929580 | 3:56,667,895 | T/A | — | uncertain significance |
| rs200904014 | 3:56,667,896 | G/T | — | benign |
| rs1315707441 | 3:56,672,770 | C/T | — | uncertain significance |
| rs775874632 | 3:56,674,082 | C/T | — | likely benign |
| rs1027626696 | 3:56,674,124 | T/C | — | uncertain significance |
| rs2472212711 | 3:56,675,498 | A/G | — | uncertain significance |
| rs2472212765 | 3:56,675,507 | C/A | — | uncertain significance |
| rs756259270 | 3:56,675,513 | G/T | — | uncertain significance |
| rs779258122 | 3:56,675,537 | G/A | — | likely benign |
| rs377557703 | 3:56,675,634 | A/G | — | uncertain significance |
| rs375228503 | 3:56,675,657 | G/A | — | uncertain significance |
| rs1185314075 | 3:56,675,680 | A/C | — | uncertain significance |
| rs753293395 | 3:56,675,703 | T/A | — | uncertain significance |
| rs755840033 | 3:56,675,718 | T/C | — | uncertain significance |
| rs376450671 | 3:56,675,766 | T/A | — | uncertain significance |
| rs376555001 | 3:56,675,768 | G/C | — | uncertain significance |
| rs1363609819 | 3:56,680,552 | T/C | — | uncertain significance |
| rs2472235361 | 3:56,680,773 | T/C | — | uncertain significance |
| rs991444132 | 3:56,680,801 | C/T | — | uncertain significance |
| rs2472235779 | 3:56,680,870 | A/C | — | uncertain significance |
| rs1027873890 | 3:56,680,877 | G/T | — | uncertain significance |
| rs754716566 | 3:56,681,120 | T/C | — | uncertain significance |
| rs144722652 | 3:56,681,126 | C/T | — | likely benign |
| rs775967397 | 3:56,683,054 | T/C | — | uncertain significance |
| rs4681724 | 3:56,687,318 | G/C | — | — |
| rs566010972 | 3:56,687,654 | T/C | — | — |
| rs374310042 | 3:56,694,810 | T/G | — | uncertain significance |
| rs377172257 | 3:56,695,029 | C/A | — | uncertain significance |
| rs7619465 | 3:56,695,060 | T/C | — | — |
| rs775908027 | 3:56,696,479 | T/C | — | uncertain significance |
| rs9845655 | 3:56,701,328 | T/C | intron variant | — |
| rs2472321258 | 3:56,703,748 | C/T | — | uncertain significance |
| rs10866000 | 3:56,705,331 | C/T | intron variant | — |
| rs1413708698 | 3:56,707,621 | A/G | — | uncertain significance |
| rs530863253 | 3:56,707,701 | A/G | — | benign |
| rs1553733337 | 3:56,716,938 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.