UBE3C
ubiquitin protein ligase E3C
Summary
Enables ubiquitin protein ligase activity. Involved in protein K29-linked ubiquitination; protein K48-linked ubiquitination; and ubiquitin-dependent protein catabolic process. Predicted to be part of proteasome complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7804018 | 7:156,943,276 | C/T | intron variant | — |
| rs3808316 | 7:156,944,787 | C/A | — | — |
| rs6946660 | 7:156,948,648 | T/A | — | — |
| rs761130106 | 7:156,961,769 | A/G | — | uncertain significance |
| rs6956046 | 7:156,962,874 | G/A | intron variant | — |
| rs371273857 | 7:156,963,004 | A/G | — | uncertain significance |
| rs543207469 | 7:156,963,064 | A/G | — | uncertain significance |
| rs766237206 | 7:156,963,115 | T/C | — | uncertain significance |
| rs140273785 | 7:156,967,619 | C/G | — | uncertain significance |
| rs150362446 | 7:156,967,643 | A/G | — | uncertain significance |
| rs149473604 | 7:156,967,664 | T/A | — | uncertain significance |
| rs1210140034 | 7:156,967,702 | A/G | — | uncertain significance |
| rs1002389 | 7:156,968,323 | C/G | intron variant | — |
| rs199836750 | 7:156,971,376 | T/C | — | benign |
| rs1194114501 | 7:156,971,398 | G/A | — | uncertain significance |
| rs1294727193 | 7:156,971,452 | C/T | — | uncertain significance |
| rs78015355 | 7:156,971,453 | G/C | — | likely benign |
| rs1481375170 | 7:156,974,284 | G/A | — | uncertain significance |
| rs17646047 | 7:156,974,354 | G/A | — | benign |
| rs376556506 | 7:156,974,888 | C/T | — | uncertain significance |
| rs769984704 | 7:156,974,953 | T/G | — | uncertain significance |
| rs1808736319 | 7:156,976,589 | G/A | — | uncertain significance |
| rs371072828 | 7:156,976,732 | C/T | — | likely benign |
| rs375277308 | 7:156,979,530 | G/C | — | uncertain significance |
| rs745679416 | 7:156,979,567 | T/A | — | uncertain significance |
| rs140842665 | 7:156,979,696 | A/G | — | uncertain significance |
| rs6950739 | 7:156,982,450 | T/C | regulatory region variant | — |
| rs11980541 | 7:156,988,776 | G/A | — | — |
| rs2366214 | 7:156,992,461 | A/G | upstream gene variant | — |
| rs2538034985 | 7:156,994,423 | A/G | — | uncertain significance |
| rs145837581 | 7:156,994,489 | G/A | — | uncertain significance |
| rs28714421 | 7:156,996,741 | G/C | — | — |
| rs371336791 | 7:157,000,096 | A/G | — | uncertain significance |
| rs761835839 | 7:157,000,132 | C/T | — | uncertain significance |
| rs2301914 | 7:157,000,176 | T/C | — | benign |
| rs2535661811 | 7:157,000,210 | T/G | — | uncertain significance |
| rs1231000016 | 7:157,000,214 | T/C | — | uncertain significance |
| rs2535661962 | 7:157,000,238 | A/G | — | uncertain significance |
| rs1328205521 | 7:157,000,415 | C/T | — | uncertain significance |
| rs747967467 | 7:157,000,420 | A/G | — | uncertain significance |
| rs888056398 | 7:157,000,459 | C/G | — | uncertain significance |
| rs117505963 | 7:157,011,936 | T/C | regulatory region variant | — |
| rs369300794 | 7:157,013,414 | A/G | — | uncertain significance |
| rs776105656 | 7:157,013,431 | C/T | — | uncertain significance |
| rs751721397 | 7:157,013,434 | A/C | — | uncertain significance |
| rs12533082 | 7:157,014,172 | T/G | — | — |
| rs373720494 | 7:157,018,171 | A/T | — | uncertain significance |
| rs1795852301 | 7:157,018,230 | A/G | — | uncertain significance |
| rs202006020 | 7:157,023,797 | C/T | — | uncertain significance |
| rs1463108717 | 7:157,023,805 | C/T | — | likely benign |
| rs754740060 | 7:157,023,885 | A/G | — | uncertain significance |
| rs1385200270 | 7:157,023,923 | A/G | — | uncertain significance |
| rs2535718927 | 7:157,023,957 | C/T | — | uncertain significance |
| rs1182444 | 7:157,024,510 | A/G | intron variant | — |
| rs1182443 | 7:157,026,052 | A/G | regulatory region variant | — |
| rs1182436 | 7:157,027,753 | T/G | — | — |
| rs369945925 | 7:157,041,270 | C/T | — | uncertain significance |
| rs150266636 | 7:157,046,707 | G/A | — | likely benign |
| rs138959964 | 7:157,046,750 | C/T | — | uncertain significance |
| rs200639306 | 7:157,046,754 | A/C | — | likely benign |
| rs376974804 | 7:157,049,634 | A/G | — | uncertain significance |
| rs1796768117 | 7:157,049,662 | G/A | — | uncertain significance |
| rs749155877 | 7:157,049,682 | C/T | — | uncertain significance |
| rs1797117735 | 7:157,060,384 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.