DTWD2
DTW motif tRNA-uridine aminocarboxypropyltransferase 2
Summary
Enables tRNA-uridine aminocarboxypropyltransferase activity. Involved in RNA glycosylation and tRNA modification. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1400359024 | 5:118,176,637 | A/C | — | uncertain significance |
| rs142887093 | 5:118,176,676 | G/C | — | uncertain significance |
| rs767918613 | 5:118,176,703 | A/G | — | uncertain significance |
| rs1405045743 | 5:118,176,721 | C/A | — | uncertain significance |
| rs753917662 | 5:118,176,722 | G/A | — | uncertain significance |
| rs140154641 | 5:118,176,772 | C/T | — | uncertain significance |
| rs538930463 | 5:118,183,789 | T/C | — | uncertain significance |
| rs148574499 | 5:118,183,823 | C/T | — | uncertain significance |
| rs2531274440 | 5:118,183,829 | C/G | — | uncertain significance |
| rs368909066 | 5:118,183,832 | C/T | — | uncertain significance |
| rs774329360 | 5:118,183,859 | T/C | — | uncertain significance |
| rs183646069 | 5:118,183,865 | G/A | — | uncertain significance |
| rs547300358 | 5:118,217,848 | G/A | — | — |
| rs377520092 | 5:118,264,237 | T/C | — | uncertain significance |
| rs200186053 | 5:118,264,309 | T/C | — | uncertain significance |
| rs751477435 | 5:118,264,411 | A/C | — | uncertain significance |
| rs748293505 | 5:118,274,895 | C/T | — | uncertain significance |
| rs200486968 | 5:118,274,913 | C/T | — | uncertain significance |
| rs375892597 | 5:118,274,969 | C/T | — | uncertain significance |
| rs900940016 | 5:118,274,970 | G/A | — | uncertain significance |
| rs1381051531 | 5:118,274,979 | T/C | — | uncertain significance |
| rs2531435638 | 5:118,280,261 | G/A | — | uncertain significance |
| rs761891421 | 5:118,280,285 | G/A | — | uncertain significance |
| rs143594682 | 5:118,280,294 | T/A | — | uncertain significance |
| rs750528656 | 5:118,280,342 | C/T | — | uncertain significance |
| rs747976729 | 5:118,287,938 | C/T | — | — |
| rs185489977 | 5:118,301,116 | G/A | intron variant | — |
| rs993171664 | 5:118,323,998 | G/T | — | uncertain significance |
| rs546051310 | 5:118,324,005 | C/G | — | uncertain significance |
| rs367835549 | 5:118,324,049 | T/C | — | uncertain significance |
| rs369717811 | 5:118,324,062 | C/T | — | uncertain significance |
| rs1421254619 | 5:118,324,083 | C/A | — | uncertain significance |
| rs1755485826 | 5:118,324,098 | C/T | — | uncertain significance |
| rs992724426 | 5:118,324,103 | C/A | — | uncertain significance |
| rs773721117 | 5:118,324,124 | T/G | — | likely benign |
| rs1175211762 | 5:118,324,161 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.