SUPT3H
SPT3 homolog, SAGA and STAGA complex component
Summary
Enables transcription coactivator activity. Involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. Part of SAGA complex and transcription factor TFTC complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10948172 | 6:44,777,691 | A/G | intron variant | — |
| rs755 | 6:44,795,790 | C/T | downstream gene variant | — |
| rs12195339 | 6:44,796,179 | T/C | downstream gene variant | — |
| rs1768289999 | 6:44,797,588 | A/G | — | uncertain significance |
| rs3799977 | 6:44,837,356 | T/G | regulatory region variant | — |
| rs554544779 | 6:44,839,647 | G/A | — | — |
| rs9349305 | 6:44,855,268 | T/C | intron variant | — |
| rs13192457 | 6:44,855,391 | C/A | — | — |
| rs3957281 | 6:44,867,834 | G/T | — | — |
| rs3957282 | 6:44,867,836 | C/T | downstream gene variant | — |
| rs538801 | 6:44,875,762 | A/T | intron variant | — |
| rs10948183 | 6:44,880,881 | T/C | intron variant | — |
| rs634789 | 6:44,896,518 | G/C | intron variant | — |
| rs577252940 | 6:44,900,452 | A/G | — | uncertain significance |
| rs758205609 | 6:44,900,468 | G/C | — | uncertain significance |
| rs113964926 | 6:44,921,076 | T/C | — | uncertain significance |
| rs748728560 | 6:44,922,276 | C/T | — | uncertain significance |
| rs2547353632 | 6:44,929,563 | T/G | — | uncertain significance |
| rs9472414 | 6:44,946,506 | T/A | intron variant | — |
| rs10948197 | 6:44,967,490 | T/G | — | — |
| rs1304997860 | 6:44,971,410 | C/G | — | uncertain significance |
| rs768082837 | 6:44,971,446 | G/T | — | uncertain significance |
| rs770419769 | 6:44,971,488 | T/A | — | uncertain significance |
| rs765705248 | 6:44,971,518 | C/T | — | uncertain significance |
| rs752201958 | 6:44,982,552 | T/C | — | uncertain significance |
| rs376196104 | 6:44,982,559 | C/T | — | uncertain significance |
| rs2547643924 | 6:44,982,567 | T/C | — | uncertain significance |
| rs568863633 | 6:44,982,588 | T/A | — | uncertain significance |
| rs150635035 | 6:44,988,293 | C/T | — | uncertain significance |
| rs373980353 | 6:44,988,294 | G/A | — | uncertain significance |
| rs764815982 | 6:44,988,302 | A/G | — | uncertain significance |
| rs766063447 | 6:44,988,333 | C/T | — | uncertain significance |
| rs192349059 | 6:44,990,192 | C/A | intron variant | — |
| rs537575728 | 6:45,031,258 | A/T | — | — |
| rs372964153 | 6:45,031,388 | A/G | — | — |
| rs1799212695 | 6:45,073,697 | A/C | — | uncertain significance |
| rs764738805 | 6:45,073,714 | A/C | — | uncertain significance |
| rs1324538 | 6:45,080,144 | T/G | — | — |
| rs9367218 | 6:45,088,179 | G/T | — | — |
| rs9357471 | 6:45,090,977 | C/T | regulatory region variant | — |
| rs9395066 | 6:45,095,163 | A/T | — | — |
| rs184065563 | 6:45,144,224 | G/C | — | — |
| rs376649957 | 6:45,145,325 | G/A | — | — |
| rs12193102 | 6:45,145,402 | C/A | — | — |
| rs191485704 | 6:45,153,183 | G/T | regulatory region variant | — |
| rs75523462 | 6:45,157,720 | T/G | intron variant | — |
| rs6941169 | 6:45,173,552 | A/T | — | — |
| rs10456544 | 6:45,181,694 | T/A | intron variant | — |
| rs72857080 | 6:45,198,373 | G/A | intron variant | — |
| rs10948222 | 6:45,244,415 | T/C | intron variant | — |
| rs4631280 | 6:45,249,290 | C/G | — | — |
| rs4441951 | 6:45,250,814 | T/A | — | — |
| rs12191751 | 6:45,282,111 | G/T | regulatory region variant | — |
| rs74551305 | 6:45,283,663 | T/C | intron variant | — |
| rs62400317 | 6:45,284,923 | C/A | — | — |
| rs188596507 | 6:45,289,532 | C/A | — | likely benign |
| rs1350563087 | 6:45,289,534 | T/C | — | uncertain significance |
| rs776717193 | 6:45,289,563 | T/C | — | likely benign |
| rs555481978 | 6:45,289,615 | T/C | — | uncertain significance |
| rs371911961 | 6:45,290,638 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.