ADAT1
adenosine deaminase tRNA specific 1
Summary
This gene is a member of the ADAR (adenosine deaminase acting on RNA) family. Using site-specific adenosine modification, proteins encoded by these genes participate in the pre-mRNA editing of nuclear transcripts. The protein encoded by this gene, tRNA-specific adenosine deaminase 1, is responsible for the deamination of adenosine 37 to inosine in eukaryotic tRNA. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2010]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs776176191 | 16:75,634,158 | C/G | — | uncertain significance |
| rs754878846 | 16:75,634,205 | G/A | — | uncertain significance |
| rs749428527 | 16:75,636,989 | G/A | — | uncertain significance |
| rs761013553 | 16:75,637,008 | T/C | — | uncertain significance |
| rs2081422909 | 16:75,642,149 | T/C | — | uncertain significance |
| rs147999655 | 16:75,642,161 | T/C | — | uncertain significance |
| rs762604498 | 16:75,642,179 | G/A | — | uncertain significance |
| rs150544374 | 16:75,642,219 | T/C | — | uncertain significance |
| rs751762218 | 16:75,642,792 | C/G | — | uncertain significance |
| rs762132802 | 16:75,642,794 | G/A | — | uncertain significance |
| rs1490648457 | 16:75,642,865 | T/A | — | uncertain significance |
| rs1478491353 | 16:75,642,882 | G/C | — | uncertain significance |
| rs768314305 | 16:75,646,158 | C/A | — | uncertain significance |
| rs374448543 | 16:75,646,227 | C/A | — | likely benign |
| rs1462755168 | 16:75,646,256 | C/T | — | uncertain significance |
| rs745981176 | 16:75,646,259 | G/A | — | uncertain significance |
| rs199507210 | 16:75,646,270 | C/T | — | uncertain significance |
| rs1222009330 | 16:75,646,309 | T/C | — | uncertain significance |
| rs756353591 | 16:75,646,358 | C/A | — | uncertain significance |
| rs755063906 | 16:75,646,363 | G/A | — | uncertain significance |
| rs562128733 | 16:75,646,367 | T/C | — | uncertain significance |
| rs138724951 | 16:75,646,462 | G/C | — | uncertain significance |
| rs117402310 | 16:75,646,491 | G/A | — | likely benign |
| rs560668562 | 16:75,646,501 | G/A | — | uncertain significance |
| rs193920811 | 16:75,646,510 | G/C | — | uncertain significance |
| rs748053472 | 16:75,646,552 | C/T | — | uncertain significance |
| rs374204618 | 16:75,646,563 | C/G | — | uncertain significance |
| rs368488673 | 16:75,646,574 | C/T | — | uncertain significance |
| rs754541349 | 16:75,646,607 | C/T | — | uncertain significance |
| rs536106427 | 16:75,646,659 | A/T | — | uncertain significance |
| rs144186738 | 16:75,651,097 | C/T | — | uncertain significance |
| rs1436996438 | 16:75,651,154 | G/A | — | uncertain significance |
| rs117176260 | 16:75,654,536 | C/T | — | likely benign |
| rs150142918 | 16:75,654,541 | T/C | — | uncertain significance |
| rs775552444 | 16:75,654,549 | G/T | — | uncertain significance |
| rs770664031 | 16:75,654,599 | T/A | — | uncertain significance |
| rs369100478 | 16:75,654,685 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.