TRMO
tRNA methyltransferase O
Summary
Enables tRNA (L-threonylcarbamoyladenosine(37)-C2) methyltransferase activity. Involved in tRNA methylation. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10818239 | 9:100,661,191 | G/T | — | — |
| rs753673780 | 9:100,667,076 | G/A | — | uncertain significance |
| rs774866546 | 9:100,667,135 | G/C | — | uncertain significance |
| rs1221120608 | 9:100,667,163 | T/C | — | uncertain significance |
| rs764943636 | 9:100,667,178 | C/A | — | uncertain significance |
| rs778202358 | 9:100,667,199 | G/A | — | uncertain significance |
| rs763559877 | 9:100,667,223 | C/T | — | likely benign |
| rs1221142895 | 9:100,672,413 | G/T | — | uncertain significance |
| rs2490073307 | 9:100,672,508 | G/A | — | uncertain significance |
| rs150271508 | 9:100,672,512 | C/T | — | likely benign |
| rs146891219 | 9:100,672,523 | T/G | — | uncertain significance |
| rs2490073546 | 9:100,672,536 | A/C | — | uncertain significance |
| rs777707868 | 9:100,672,632 | T/C | — | uncertain significance |
| rs777236790 | 9:100,672,809 | G/C | — | uncertain significance |
| rs758783430 | 9:100,672,830 | T/C | — | uncertain significance |
| rs558175701 | 9:100,672,851 | C/T | — | uncertain significance |
| rs200779838 | 9:100,672,862 | T/C | — | uncertain significance |
| rs141236958 | 9:100,675,724 | T/C | — | uncertain significance |
| rs754529337 | 9:100,675,769 | C/T | — | uncertain significance |
| rs77668890 | 9:100,675,777 | C/T | — | benign |
| rs201918701 | 9:100,675,817 | T/C | — | uncertain significance |
| rs3780419 | 9:100,677,134 | T/C | upstream gene variant | — |
| rs760135051 | 9:100,678,474 | T/C | — | uncertain significance |
| rs2490099834 | 9:100,678,488 | G/A | — | uncertain significance |
| rs1284551328 | 9:100,678,557 | G/C | — | uncertain significance |
| rs7864655 | 9:100,679,836 | T/G | downstream gene variant | — |
| rs10984377 | 9:100,684,534 | A/C | — | — |
| rs1451571939 | 9:100,684,721 | C/A | — | uncertain significance |
| rs758172189 | 9:100,684,724 | A/G | — | uncertain significance |
| rs376128350 | 9:100,684,735 | G/A | — | uncertain significance |
| rs150014670 | 9:100,684,751 | G/A | — | uncertain significance |
| rs3808894 | 9:100,686,129 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.