TULP4
TUB like protein 4
Summary
Predicted to be involved in protein ubiquitination. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants161 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs184871652 | 6:158,704,513 | G/A | intron variant | — |
| rs11758177 | 6:158,731,038 | A/G | upstream gene variant | — |
| rs763597902 | 6:158,735,121 | C/T | — | uncertain significance |
| rs780896544 | 6:158,735,148 | C/G | — | uncertain significance |
| rs1045091320 | 6:158,735,257 | C/T | — | uncertain significance |
| rs1324493664 | 6:158,735,283 | C/T | — | uncertain significance |
| rs1235266039 | 6:158,735,293 | A/G | — | uncertain significance |
| rs141133811 | 6:158,735,298 | G/A | — | uncertain significance |
| rs6933038 | 6:158,737,649 | T/C | — | — |
| rs10806695 | 6:158,738,692 | T/A | — | — |
| rs2105333 | 6:158,755,437 | T/C | — | — |
| rs341141 | 6:158,809,708 | A/G | intron variant | — |
| rs1396439861 | 6:158,834,214 | C/T | — | uncertain significance |
| rs341147 | 6:158,841,725 | A/G | intron variant | — |
| rs375882472 | 6:158,850,781 | C/T | — | uncertain significance |
| rs755898916 | 6:158,850,868 | C/T | — | uncertain significance |
| rs138932674 | 6:158,850,899 | G/A | — | likely benign |
| rs34360218 | 6:158,870,094 | G/A | — | uncertain significance |
| rs764504122 | 6:158,870,115 | G/C | — | uncertain significance |
| rs138899998 | 6:158,870,140 | A/T | — | uncertain significance |
| rs770829194 | 6:158,873,183 | C/T | — | uncertain significance |
| rs149734049 | 6:158,873,256 | A/G | — | uncertain significance |
| rs41266333 | 6:158,873,293 | G/A | — | likely benign |
| rs940536194 | 6:158,873,294 | C/A | — | uncertain significance |
| rs571390699 | 6:158,875,053 | G/A | — | — |
| rs10698713 | 6:158,882,320 | G/A | intron variant | — |
| rs771310062 | 6:158,882,651 | C/T | — | uncertain significance |
| rs536921467 | 6:158,882,678 | A/G | — | uncertain significance |
| rs1339293129 | 6:158,882,679 | A/G | — | uncertain significance |
| rs143465123 | 6:158,894,990 | C/T | intron variant | — |
| rs142094605 | 6:158,900,828 | T/C | — | likely benign |
| rs151289701 | 6:158,900,874 | G/A | — | uncertain significance |
| rs1421032856 | 6:158,900,912 | G/A | — | uncertain significance |
| rs150475135 | 6:158,900,925 | G/A | — | uncertain significance |
| rs536877214 | 6:158,900,932 | C/G | — | uncertain significance |
| rs138487081 | 6:158,900,939 | G/A | — | uncertain significance |
| rs138863746 | 6:158,902,103 | C/T | — | uncertain significance |
| rs753219213 | 6:158,902,172 | G/A | — | uncertain significance |
| rs776920426 | 6:158,902,202 | C/T | — | uncertain significance |
| rs200691398 | 6:158,902,211 | C/G | — | uncertain significance |
| rs374889085 | 6:158,902,259 | G/A | — | uncertain significance |
| rs749380819 | 6:158,902,288 | G/A | — | uncertain significance |
| rs144739382 | 6:158,902,313 | G/A | — | uncertain significance |
| rs116229832 | 6:158,908,452 | A/G | intron variant | — |
| rs141271573 | 6:158,910,653 | T/C | — | uncertain significance |
| rs2483801195 | 6:158,910,685 | G/T | — | uncertain significance |
| rs2483801692 | 6:158,910,715 | A/G | — | uncertain significance |
| rs139803752 | 6:158,910,724 | C/T | — | uncertain significance |
| rs61742077 | 6:158,910,743 | G/A | — | likely benign |
| rs752755828 | 6:158,910,755 | A/G | — | uncertain significance |
| rs2483802353 | 6:158,910,767 | A/C | — | uncertain significance |
| rs746537100 | 6:158,914,673 | G/A | — | uncertain significance |
| rs1780264668 | 6:158,914,684 | C/T | — | uncertain significance |
| rs150873405 | 6:158,914,699 | G/C | — | uncertain significance |
| rs751015565 | 6:158,914,717 | C/T | — | uncertain significance |
| rs1245163706 | 6:158,915,798 | C/G | — | uncertain significance |
| rs527631392 | 6:158,919,767 | G/A | — | uncertain significance |
| rs1279059309 | 6:158,919,785 | A/G | — | uncertain significance |
| rs2483900519 | 6:158,922,710 | T/C | — | uncertain significance |
| rs577929133 | 6:158,922,785 | C/T | — | uncertain significance |
| rs2483901168 | 6:158,922,798 | G/T | — | uncertain significance |
| rs775084559 | 6:158,922,827 | A/G | — | uncertain significance |
| rs372165583 | 6:158,922,878 | C/T | — | uncertain significance |
| rs377659848 | 6:158,922,886 | G/A | — | uncertain significance |
| rs1391270469 | 6:158,922,926 | A/T | — | uncertain significance |
| rs1780453782 | 6:158,922,939 | C/G | — | uncertain significance |
| rs775316063 | 6:158,922,941 | G/A | — | uncertain significance |
| rs369570435 | 6:158,922,976 | G/A | — | uncertain significance |
| rs200671698 | 6:158,922,989 | G/A | — | uncertain significance |
| rs34386232 | 6:158,923,029 | G/A | — | benign |
| rs2483904307 | 6:158,923,051 | T/C | — | uncertain significance |
| rs150422279 | 6:158,923,055 | C/T | — | uncertain significance |
| rs750807378 | 6:158,923,057 | G/A | — | uncertain significance |
| rs534676989 | 6:158,923,111 | C/T | — | uncertain significance |
| rs138229082 | 6:158,923,120 | C/A | — | likely benign |
| rs760926230 | 6:158,923,202 | C/T | — | uncertain significance |
| rs2483908173 | 6:158,923,298 | G/A | — | uncertain significance |
| rs753648417 | 6:158,923,319 | C/T | — | uncertain significance |
| rs2483908539 | 6:158,923,321 | T/C | — | uncertain significance |
| rs1039643204 | 6:158,923,399 | C/T | — | uncertain significance |
| rs138201740 | 6:158,923,400 | G/A | — | uncertain significance |
| rs141158549 | 6:158,923,451 | C/T | — | uncertain significance |
| rs2483910191 | 6:158,923,458 | C/G | — | uncertain significance |
| rs374416132 | 6:158,923,478 | C/T | — | uncertain significance |
| rs367875154 | 6:158,923,528 | C/T | — | uncertain significance |
| rs751772422 | 6:158,923,544 | G/C | — | uncertain significance |
| rs1328901401 | 6:158,923,564 | G/C | — | uncertain significance |
| rs779080360 | 6:158,923,571 | C/T | — | uncertain significance |
| rs115368748 | 6:158,923,574 | C/T | — | uncertain significance |
| rs1411050625 | 6:158,923,582 | G/C | — | uncertain significance |
| rs775482315 | 6:158,923,601 | C/T | — | uncertain significance |
| rs146885905 | 6:158,923,610 | G/C | — | uncertain significance |
| rs1405703999 | 6:158,923,644 | C/G | — | uncertain significance |
| rs200667552 | 6:158,923,657 | C/T | — | uncertain significance |
| rs143675661 | 6:158,923,658 | G/A | — | uncertain significance |
| rs201288009 | 6:158,923,711 | C/T | — | uncertain significance |
| rs34762353 | 6:158,923,722 | G/A | — | likely benign |
| rs765123369 | 6:158,923,732 | G/A | — | uncertain significance |
| rs750371896 | 6:158,923,753 | G/T | — | uncertain significance |
| rs750760884 | 6:158,923,786 | C/G | — | uncertain significance |
Showing 100 of 161 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.