AK9
adenylate kinase 9
Summary
The protein encoded by this gene catalyzes the interconversion of nucleosides, possessing both nucleoside monophosphate and diphosphate kinase activities. The encoded protein uses these interconversions to maintain nucleoside homeostasis. [provided by RefSeq, Jul 2016]
Known Variants106 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs745845806 | 6:109,814,585 | G/T | — | uncertain significance |
| rs1309917329 | 6:109,814,589 | C/A | — | uncertain significance |
| rs770704105 | 6:109,814,754 | C/T | — | uncertain significance |
| rs749260551 | 6:109,815,228 | C/T | — | uncertain significance |
| rs144374788 | 6:109,816,584 | G/A | — | uncertain significance |
| rs9487128 | 6:109,818,706 | A/G | — | benign |
| rs778290881 | 6:109,819,062 | C/T | — | uncertain significance |
| rs778297280 | 6:109,819,099 | T/G | — | uncertain significance |
| rs138960025 | 6:109,819,135 | G/A | — | uncertain significance |
| rs754683982 | 6:109,820,332 | A/G | — | uncertain significance |
| rs749268272 | 6:109,820,389 | C/T | — | uncertain significance |
| rs73520970 | 6:109,820,397 | C/T | — | benign |
| rs145186563 | 6:109,820,430 | G/A | — | benign |
| rs569782612 | 6:109,820,438 | C/T | — | uncertain significance |
| rs79674254 | 6:109,822,281 | C/A | upstream gene variant | — |
| rs3056655 | 6:109,824,194 | A/T | — | — |
| rs115666311 | 6:109,827,606 | C/A | — | benign |
| rs2483041951 | 6:109,827,694 | T/C | — | uncertain significance |
| rs78704011 | 6:109,827,729 | A/G | — | benign |
| rs766302123 | 6:109,827,734 | G/A | — | uncertain significance |
| rs1336004877 | 6:109,827,946 | C/A | — | uncertain significance |
| rs10457194 | 6:109,828,569 | T/A | downstream gene variant | — |
| rs1426545621 | 6:109,830,481 | A/G | — | uncertain significance |
| rs767574558 | 6:109,830,502 | G/A | — | uncertain significance |
| rs1385696916 | 6:109,830,580 | G/T | — | uncertain significance |
| rs1779042285 | 6:109,835,456 | A/G | — | uncertain significance |
| rs754757277 | 6:109,835,573 | C/T | — | uncertain significance |
| rs377231883 | 6:109,835,600 | T/C | — | uncertain significance |
| rs777713341 | 6:109,837,199 | T/C | — | uncertain significance |
| rs766622607 | 6:109,837,215 | C/G | — | uncertain significance |
| rs931444199 | 6:109,837,230 | G/A | — | uncertain significance |
| rs2483170409 | 6:109,837,255 | T/C | — | uncertain significance |
| rs375441074 | 6:109,837,694 | C/T | — | uncertain significance |
| rs138106785 | 6:109,850,233 | C/A | — | uncertain significance |
| rs150584003 | 6:109,850,242 | A/G | — | uncertain significance |
| rs753792386 | 6:109,854,459 | T/G | — | uncertain significance |
| rs569544713 | 6:109,854,474 | C/T | — | uncertain significance |
| rs755288597 | 6:109,854,485 | T/G | — | uncertain significance |
| rs754985413 | 6:109,854,612 | C/A | — | uncertain significance |
| rs574889890 | 6:109,854,633 | C/T | — | uncertain significance |
| rs149657724 | 6:109,854,641 | C/T | — | uncertain significance |
| rs148570357 | 6:109,858,629 | C/A | — | — |
| rs13201951 | 6:109,861,294 | C/A | — | — |
| rs140622664 | 6:109,867,197 | T/G | — | uncertain significance |
| rs1010258550 | 6:109,867,245 | A/G | — | uncertain significance |
| rs770781581 | 6:109,867,279 | T/G | — | likely benign |
| rs146551987 | 6:109,871,321 | T/C | — | uncertain significance |
| rs746980960 | 6:109,871,384 | C/T | — | uncertain significance |
| rs149506107 | 6:109,871,399 | T/G | — | uncertain significance |
| rs951224133 | 6:109,871,427 | A/C | — | uncertain significance |
| rs2483677190 | 6:109,871,428 | G/C | — | uncertain significance |
| rs1311587628 | 6:109,871,505 | C/T | — | uncertain significance |
| rs755975965 | 6:109,884,903 | T/C | — | uncertain significance |
| rs1303161131 | 6:109,885,322 | G/A | — | uncertain significance |
| rs776998087 | 6:109,885,338 | C/A | — | uncertain significance |
| rs201166033 | 6:109,885,417 | T/G | — | uncertain significance |
| rs1397498405 | 6:109,885,452 | A/G | — | likely benign |
| rs1204130200 | 6:109,885,474 | G/A | — | pathogenic |
| rs10499052 | 6:109,885,475 | A/G | — | benign |
| rs760659887 | 6:109,885,967 | G/T | — | uncertain significance |
| rs7757895 | 6:109,886,005 | T/C | — | benign |
| rs2483910785 | 6:109,886,008 | G/C | — | uncertain significance |
| rs755163915 | 6:109,886,035 | G/C | — | uncertain significance |
| rs538453902 | 6:109,894,704 | C/T | — | uncertain significance |
| rs149966526 | 6:109,894,709 | G/A | — | benign |
| rs376413273 | 6:109,894,735 | C/T | — | uncertain significance |
| rs188116177 | 6:109,894,745 | C/A | — | uncertain significance |
| rs775154259 | 6:109,900,784 | C/G | — | uncertain significance |
| rs967714289 | 6:109,900,803 | A/T | — | uncertain significance |
| rs1392053431 | 6:109,906,335 | T/G | — | uncertain significance |
| rs796660929 | 6:109,907,189 | C/A | — | uncertain significance |
| rs939082859 | 6:109,907,221 | T/G | — | uncertain significance |
| rs765503791 | 6:109,931,669 | C/T | — | uncertain significance |
| rs775759266 | 6:109,931,690 | C/T | — | uncertain significance |
| rs114438747 | 6:109,931,720 | A/G | — | benign |
| rs114738991 | 6:109,935,453 | G/C | — | benign |
| rs1793902365 | 6:109,935,472 | C/T | — | uncertain significance |
| rs373758705 | 6:109,935,494 | T/C | — | uncertain significance |
| rs9372219 | 6:109,935,578 | A/G | — | benign |
| rs867574663 | 6:109,935,599 | A/T | — | uncertain significance |
| rs186032348 | 6:109,935,630 | C/T | — | uncertain significance |
| rs79239765 | 6:109,940,289 | T/C | — | benign |
| rs771301863 | 6:109,940,344 | A/C | — | uncertain significance |
| rs11758649 | 6:109,950,854 | G/A | — | — |
| rs113588284 | 6:109,954,107 | C/T | — | uncertain significance |
| rs79604737 | 6:109,954,114 | T/A | — | uncertain significance |
| rs148265781 | 6:109,954,150 | C/T | — | uncertain significance |
| rs754881003 | 6:109,954,230 | G/A | — | uncertain significance |
| rs139521783 | 6:109,954,264 | T/C | — | likely benign |
| rs200088189 | 6:109,954,427 | C/T | — | uncertain significance |
| rs752260423 | 6:109,954,474 | C/T | — | uncertain significance |
| rs75582269 | 6:109,954,498 | T/C | — | benign |
| rs748811862 | 6:109,954,523 | C/T | — | uncertain significance |
| rs1797820753 | 6:109,965,834 | C/T | — | uncertain significance |
| rs2485202570 | 6:109,965,836 | G/T | — | uncertain significance |
| rs151265370 | 6:109,965,891 | C/T | — | uncertain significance |
| rs140510249 | 6:109,977,967 | T/C | — | uncertain significance |
| rs150128474 | 6:109,977,977 | T/C | — | likely benign |
| rs765324802 | 6:109,978,075 | C/T | — | uncertain significance |
| rs2485526821 | 6:109,980,443 | T/A | — | uncertain significance |
Showing 100 of 106 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.