TRIM71
tripartite motif containing 71
Summary
The protein encoded by this gene is an E3 ubiquitin-protein ligase that binds with miRNAs and maintains the growth and upkeep of embryonic stem cells. This gene also is involved in the G1-S phase transition of the cell cycle. [provided by RefSeq, Dec 2015]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs746524808 | 3:32,859,585 | C/G | — | uncertain significance |
| rs994302824 | 3:32,859,671 | G/C | — | likely benign |
| rs748901412 | 3:32,859,691 | C/T | — | uncertain significance |
| rs1270384396 | 3:32,859,771 | C/A | — | uncertain significance |
| rs1410832868 | 3:32,859,802 | C/G | — | uncertain significance |
| rs908592994 | 3:32,859,809 | C/T | — | likely benign |
| rs1284064696 | 3:32,859,820 | C/T | — | uncertain significance |
| rs1293435424 | 3:32,859,911 | C/T | — | likely benign |
| rs1696084349 | 3:32,859,940 | T/C | — | uncertain significance |
| rs752609896 | 3:32,859,946 | C/T | — | uncertain significance |
| rs1002341005 | 3:32,860,027 | A/C | — | uncertain significance |
| rs960944177 | 3:32,860,030 | C/T | — | uncertain significance |
| rs961347389 | 3:32,860,057 | C/T | — | uncertain significance |
| rs781320370 | 3:32,860,125 | G/T | — | conflicting classifications of pathogenicity |
| rs773330912 | 3:32,860,135 | C/A | — | uncertain significance |
| rs761428558 | 3:32,860,155 | C/A | — | uncertain significance |
| rs2471020878 | 3:32,860,194 | G/A | — | uncertain significance |
| rs2471021164 | 3:32,860,279 | A/G | — | likely pathogenic |
| rs1202030458 | 3:32,860,309 | G/C | — | likely benign |
| rs200612822 | 3:32,860,343 | G/A | — | likely benign |
| rs746139247 | 3:32,860,348 | C/G | — | uncertain significance |
| rs769421964 | 3:32,860,357 | G/C | — | likely benign |
| rs1363812189 | 3:32,860,375 | T/A | — | uncertain significance |
| rs56131903 | 3:32,879,823 | A/T | intron variant | — |
| rs75746811 | 3:32,906,911 | G/A | regulatory region variant | — |
| rs73044199 | 3:32,914,555 | T/C | — | — |
| rs184943378 | 3:32,915,303 | T/C | — | benign |
| rs147066271 | 3:32,915,405 | G/A | — | likely benign |
| rs2471079085 | 3:32,915,424 | G/A | — | uncertain significance |
| rs781070829 | 3:32,915,464 | G/A | — | uncertain significance |
| rs7616050 | 3:32,920,901 | C/T | — | — |
| rs771272076 | 3:32,927,454 | C/T | — | uncertain significance |
| rs2471089203 | 3:32,927,467 | G/C | — | uncertain significance |
| rs536248483 | 3:32,927,475 | C/T | — | uncertain significance |
| rs752251831 | 3:32,927,515 | G/C | — | uncertain significance |
| rs372719076 | 3:32,927,522 | A/C | — | uncertain significance |
| rs2471089366 | 3:32,927,540 | G/A | — | uncertain significance |
| rs9310995 | 3:32,929,115 | T/C | intron variant | — |
| rs747471675 | 3:32,931,917 | C/A | — | uncertain significance |
| rs781229786 | 3:32,931,936 | A/T | — | uncertain significance |
| rs748268178 | 3:32,932,039 | G/A | — | uncertain significance |
| rs754169136 | 3:32,932,148 | C/G | — | likely benign |
| rs372088601 | 3:32,932,182 | C/T | — | uncertain significance |
| rs2471094455 | 3:32,932,230 | C/G | — | uncertain significance |
| rs558049901 | 3:32,932,245 | C/T | — | uncertain significance |
| rs2471094479 | 3:32,932,253 | A/T | — | likely benign |
| rs1697016744 | 3:32,932,309 | C/G | — | uncertain significance |
| rs200204603 | 3:32,932,354 | G/A | — | uncertain significance |
| rs1559552272 | 3:32,932,462 | T/C | — | uncertain significance |
| rs771625560 | 3:32,932,473 | G/A | — | uncertain significance |
| rs201860756 | 3:32,932,485 | G/A | — | conflicting classifications of pathogenicity |
| rs1575362216 | 3:32,932,519 | G/A | — | pathogenic |
| rs1575362239 | 3:32,932,582 | G/A | — | likely pathogenic |
| rs2125693638 | 3:32,932,602 | T/C | — | uncertain significance |
| rs200356061 | 3:32,932,642 | G/A | — | uncertain significance |
| rs184923688 | 3:32,932,655 | C/T | — | likely benign |
| rs2471095157 | 3:32,932,738 | C/T | — | uncertain significance |
| rs1483016798 | 3:32,932,825 | C/G | — | uncertain significance |
| rs200564131 | 3:32,932,841 | G/A | — | likely benign |
| rs1414862774 | 3:32,932,915 | A/G | — | uncertain significance |
| rs112979410 | 3:32,933,006 | G/T | — | likely benign |
| rs779223962 | 3:32,933,025 | G/A | — | uncertain significance |
| rs747205413 | 3:32,933,044 | T/C | — | uncertain significance |
| rs201763394 | 3:32,933,068 | A/G | — | uncertain significance |
| rs774383473 | 3:32,933,075 | G/T | — | uncertain significance |
| rs1575362492 | 3:32,933,083 | G/A | — | pathogenic |
| rs75763149 | 3:32,933,129 | G/A | — | benign |
| rs1045177462 | 3:32,933,146 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.