UGT3A1
UDP glycosyltransferase family 3 member A1
Summary
Enables glucuronosyltransferase activity. Part of UDP-N-acetylglucosamine transferase complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1739264211 | 5:35,954,327 | C/G | — | uncertain significance |
| rs374910980 | 5:35,954,375 | A/C | — | uncertain significance |
| rs370982147 | 5:35,954,470 | G/A | — | uncertain significance |
| rs141907677 | 5:35,954,473 | G/A | — | uncertain significance |
| rs2531695646 | 5:35,954,492 | T/C | — | uncertain significance |
| rs201908500 | 5:35,954,499 | G/C | — | uncertain significance |
| rs200660217 | 5:35,954,522 | C/T | — | uncertain significance |
| rs768343985 | 5:35,954,530 | A/G | — | uncertain significance |
| rs199844466 | 5:35,955,770 | C/T | — | uncertain significance |
| rs761985145 | 5:35,955,848 | C/T | — | uncertain significance |
| rs191737460 | 5:35,955,850 | T/C | — | uncertain significance |
| rs371955454 | 5:35,955,851 | G/C | — | uncertain significance |
| rs762872593 | 5:35,955,898 | C/T | — | uncertain significance |
| rs2531703119 | 5:35,955,913 | C/T | — | uncertain significance |
| rs539496316 | 5:35,957,331 | T/C | — | uncertain significance |
| rs747178148 | 5:35,957,347 | C/A | — | uncertain significance |
| rs535671200 | 5:35,957,423 | C/G | — | uncertain significance |
| rs2531709847 | 5:35,957,456 | C/T | — | uncertain significance |
| rs558891923 | 5:35,961,131 | C/T | — | — |
| rs144263859 | 5:35,965,574 | A/G | — | uncertain significance |
| rs759699054 | 5:35,965,630 | C/T | — | uncertain significance |
| rs1476936784 | 5:35,965,645 | A/T | — | uncertain significance |
| rs200732514 | 5:35,965,672 | G/A | — | uncertain significance |
| rs184564491 | 5:35,965,682 | T/G | — | likely benign |
| rs763116023 | 5:35,965,747 | A/C | — | uncertain significance |
| rs949588732 | 5:35,965,768 | G/C | — | uncertain significance |
| rs141076093 | 5:35,965,820 | C/T | — | uncertain significance |
| rs1336923707 | 5:35,965,859 | G/T | — | uncertain significance |
| rs901483716 | 5:35,965,861 | T/C | — | uncertain significance |
| rs2531742601 | 5:35,965,879 | G/C | — | uncertain significance |
| rs10491431 | 5:35,968,000 | C/G | — | — |
| rs747333133 | 5:35,968,124 | C/A | — | uncertain significance |
| rs1220014934 | 5:35,968,126 | A/T | — | uncertain significance |
| rs760064814 | 5:35,968,143 | T/C | — | likely benign |
| rs1270791283 | 5:35,968,209 | G/C | — | uncertain significance |
| rs1739888653 | 5:35,968,212 | A/G | — | uncertain significance |
| rs4869450 | 5:35,968,843 | T/A | intron variant | — |
| rs12659258 | 5:35,970,215 | G/A | intron variant | — |
| rs10070851 | 5:35,974,188 | A/T | intron variant | — |
| rs141178097 | 5:35,974,885 | C/T | intron variant | — |
| rs113590482 | 5:35,979,545 | G/T | intron variant | — |
| rs6889699 | 5:35,980,475 | C/T | intron variant | — |
| rs2531827601 | 5:35,988,567 | T/G | — | uncertain significance |
| rs112329668 | 5:35,990,440 | A/G | intron variant | — |
| rs4616927 | 5:35,997,898 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.