ADAD2
adenosine deaminase domain containing 2
Summary
Predicted to enable double-stranded RNA adenosine deaminase activity; double-stranded RNA binding activity; and tRNA-specific adenosine deaminase activity. Predicted to be involved in RNA processing; adenosine to inosine editing; and spermatid development. Predicted to be located in nucleus. Predicted to be active in cytoplasm and nucleolus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants67 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1469832701 | 16:84,224,844 | C/T | — | uncertain significance |
| rs778628327 | 16:84,224,849 | T/G | — | likely benign |
| rs146687643 | 16:84,224,856 | G/T | — | uncertain significance |
| rs143424699 | 16:84,224,872 | C/T | — | likely benign |
| rs769615300 | 16:84,224,895 | C/G | — | uncertain significance |
| rs759599115 | 16:84,224,922 | C/G | — | uncertain significance |
| rs2089647483 | 16:84,224,925 | G/A | — | uncertain significance |
| rs1443186141 | 16:84,224,943 | C/T | — | uncertain significance |
| rs767625659 | 16:84,224,958 | G/A | — | uncertain significance |
| rs2507718646 | 16:84,224,960 | G/T | — | uncertain significance |
| rs749448838 | 16:84,225,039 | G/A | — | uncertain significance |
| rs1158475243 | 16:84,225,051 | G/A | — | uncertain significance |
| rs537718186 | 16:84,225,057 | G/A | — | uncertain significance |
| rs2507719113 | 16:84,225,077 | G/A | — | uncertain significance |
| rs373376587 | 16:84,225,080 | C/T | — | uncertain significance |
| rs997900127 | 16:84,225,134 | C/T | — | uncertain significance |
| rs1163502298 | 16:84,225,144 | G/T | — | uncertain significance |
| rs2089654827 | 16:84,225,171 | C/T | — | uncertain significance |
| rs529653331 | 16:84,225,198 | C/G | — | uncertain significance |
| rs1014702043 | 16:84,225,207 | C/A | — | uncertain significance |
| rs1468630925 | 16:84,227,639 | G/A | — | uncertain significance |
| rs763593645 | 16:84,227,672 | A/C | — | uncertain significance |
| rs571312243 | 16:84,227,714 | G/A | — | uncertain significance |
| rs778730837 | 16:84,227,774 | C/T | — | uncertain significance |
| rs143178381 | 16:84,227,786 | T/C | — | uncertain significance |
| rs774334290 | 16:84,228,066 | C/T | — | uncertain significance |
| rs199517310 | 16:84,228,159 | G/A | — | uncertain significance |
| rs151198178 | 16:84,228,167 | C/T | — | uncertain significance |
| rs759059385 | 16:84,228,168 | G/A | — | likely benign |
| rs774543669 | 16:84,228,560 | G/A | — | likely benign |
| rs983695805 | 16:84,228,572 | C/T | — | uncertain significance |
| rs776663341 | 16:84,228,680 | A/C | — | uncertain significance |
| rs200062226 | 16:84,228,722 | G/A | — | uncertain significance |
| rs141987575 | 16:84,228,750 | C/T | — | uncertain significance |
| rs780180604 | 16:84,228,904 | A/C | — | uncertain significance |
| rs537456691 | 16:84,228,908 | C/T | — | uncertain significance |
| rs2507729525 | 16:84,228,968 | G/A | — | uncertain significance |
| rs2507729539 | 16:84,228,970 | T/A | — | likely benign |
| rs958719340 | 16:84,229,142 | G/C | — | uncertain significance |
| rs2507730167 | 16:84,229,143 | T/C | — | uncertain significance |
| rs749796902 | 16:84,229,174 | G/A | — | uncertain significance |
| rs139952223 | 16:84,229,288 | C/T | — | uncertain significance |
| rs763031674 | 16:84,229,294 | G/A | — | likely benign |
| rs1178525159 | 16:84,229,432 | C/G | — | likely benign |
| rs977470393 | 16:84,229,454 | C/A | — | uncertain significance |
| rs777631847 | 16:84,229,462 | C/A | — | uncertain significance |
| rs1354323988 | 16:84,229,501 | C/A | — | uncertain significance |
| rs2507731627 | 16:84,229,555 | C/T | — | uncertain significance |
| rs1275475341 | 16:84,229,566 | C/G | — | uncertain significance |
| rs2507731793 | 16:84,229,593 | G/A | — | uncertain significance |
| rs375522638 | 16:84,229,747 | G/A | — | uncertain significance |
| rs369532147 | 16:84,229,750 | C/T | — | uncertain significance |
| rs369743783 | 16:84,229,828 | G/A | — | uncertain significance |
| rs138265121 | 16:84,229,831 | C/T | — | uncertain significance |
| rs150807545 | 16:84,229,841 | T/C | — | uncertain significance |
| rs141742506 | 16:84,229,892 | T/C | — | uncertain significance |
| rs373054415 | 16:84,229,897 | C/G | — | uncertain significance |
| rs761512404 | 16:84,229,924 | G/C | — | uncertain significance |
| rs2089730300 | 16:84,229,939 | G/A | — | uncertain significance |
| rs759844451 | 16:84,229,957 | A/C | — | uncertain significance |
| rs200997815 | 16:84,230,257 | G/A | — | likely benign |
| rs1291939558 | 16:84,230,258 | C/T | — | uncertain significance |
| rs142962765 | 16:84,230,300 | G/T | — | uncertain significance |
| rs141107296 | 16:84,230,339 | A/G | — | uncertain significance |
| rs768492546 | 16:84,230,480 | G/C | — | uncertain significance |
| rs774185081 | 16:84,230,486 | A/G | — | uncertain significance |
| rs745974652 | 16:84,230,506 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.