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

rsidPosition (GRCh37)AllelesClassClinVar
rs7458458066:109,814,585G/Tuncertain significance
rs13099173296:109,814,589C/Auncertain significance
rs7707041056:109,814,754C/Tuncertain significance
rs7492605516:109,815,228C/Tuncertain significance
rs1443747886:109,816,584G/Auncertain significance
rs94871286:109,818,706A/Gbenign
rs7782908816:109,819,062C/Tuncertain significance
rs7782972806:109,819,099T/Guncertain significance
rs1389600256:109,819,135G/Auncertain significance
rs7546839826:109,820,332A/Guncertain significance
rs7492682726:109,820,389C/Tuncertain significance
rs735209706:109,820,397C/Tbenign
rs1451865636:109,820,430G/Abenign
rs5697826126:109,820,438C/Tuncertain significance
rs796742546:109,822,281C/Aupstream gene variant
rs30566556:109,824,194A/T
rs1156663116:109,827,606C/Abenign
rs24830419516:109,827,694T/Cuncertain significance
rs787040116:109,827,729A/Gbenign
rs7663021236:109,827,734G/Auncertain significance
rs13360048776:109,827,946C/Auncertain significance
rs104571946:109,828,569T/Adownstream gene variant
rs14265456216:109,830,481A/Guncertain significance
rs7675745586:109,830,502G/Auncertain significance
rs13856969166:109,830,580G/Tuncertain significance
rs17790422856:109,835,456A/Guncertain significance
rs7547572776:109,835,573C/Tuncertain significance
rs3772318836:109,835,600T/Cuncertain significance
rs7777133416:109,837,199T/Cuncertain significance
rs7666226076:109,837,215C/Guncertain significance
rs9314441996:109,837,230G/Auncertain significance
rs24831704096:109,837,255T/Cuncertain significance
rs3754410746:109,837,694C/Tuncertain significance
rs1381067856:109,850,233C/Auncertain significance
rs1505840036:109,850,242A/Guncertain significance
rs7537923866:109,854,459T/Guncertain significance
rs5695447136:109,854,474C/Tuncertain significance
rs7552885976:109,854,485T/Guncertain significance
rs7549854136:109,854,612C/Auncertain significance
rs5748898906:109,854,633C/Tuncertain significance
rs1496577246:109,854,641C/Tuncertain significance
rs1485703576:109,858,629C/A
rs132019516:109,861,294C/A
rs1406226646:109,867,197T/Guncertain significance
rs10102585506:109,867,245A/Guncertain significance
rs7707815816:109,867,279T/Glikely benign
rs1465519876:109,871,321T/Cuncertain significance
rs7469809606:109,871,384C/Tuncertain significance
rs1495061076:109,871,399T/Guncertain significance
rs9512241336:109,871,427A/Cuncertain significance
rs24836771906:109,871,428G/Cuncertain significance
rs13115876286:109,871,505C/Tuncertain significance
rs7559759656:109,884,903T/Cuncertain significance
rs13031611316:109,885,322G/Auncertain significance
rs7769980876:109,885,338C/Auncertain significance
rs2011660336:109,885,417T/Guncertain significance
rs13974984056:109,885,452A/Glikely benign
rs12041302006:109,885,474G/Apathogenic
rs104990526:109,885,475A/Gbenign
rs7606598876:109,885,967G/Tuncertain significance
rs77578956:109,886,005T/Cbenign
rs24839107856:109,886,008G/Cuncertain significance
rs7551639156:109,886,035G/Cuncertain significance
rs5384539026:109,894,704C/Tuncertain significance
rs1499665266:109,894,709G/Abenign
rs3764132736:109,894,735C/Tuncertain significance
rs1881161776:109,894,745C/Auncertain significance
rs7751542596:109,900,784C/Guncertain significance
rs9677142896:109,900,803A/Tuncertain significance
rs13920534316:109,906,335T/Guncertain significance
rs7966609296:109,907,189C/Auncertain significance
rs9390828596:109,907,221T/Guncertain significance
rs7655037916:109,931,669C/Tuncertain significance
rs7757592666:109,931,690C/Tuncertain significance
rs1144387476:109,931,720A/Gbenign
rs1147389916:109,935,453G/Cbenign
rs17939023656:109,935,472C/Tuncertain significance
rs3737587056:109,935,494T/Cuncertain significance
rs93722196:109,935,578A/Gbenign
rs8675746636:109,935,599A/Tuncertain significance
rs1860323486:109,935,630C/Tuncertain significance
rs792397656:109,940,289T/Cbenign
rs7713018636:109,940,344A/Cuncertain significance
rs117586496:109,950,854G/A
rs1135882846:109,954,107C/Tuncertain significance
rs796047376:109,954,114T/Auncertain significance
rs1482657816:109,954,150C/Tuncertain significance
rs7548810036:109,954,230G/Auncertain significance
rs1395217836:109,954,264T/Clikely benign
rs2000881896:109,954,427C/Tuncertain significance
rs7522604236:109,954,474C/Tuncertain significance
rs755822696:109,954,498T/Cbenign
rs7488118626:109,954,523C/Tuncertain significance
rs17978207536:109,965,834C/Tuncertain significance
rs24852025706:109,965,836G/Tuncertain significance
rs1512653706:109,965,891C/Tuncertain significance
rs1405102496:109,977,967T/Cuncertain significance
rs1501284746:109,977,977T/Clikely benign
rs7653248026:109,978,075C/Tuncertain significance
rs24855268216:109,980,443T/Auncertain significance

Showing 100 of 106 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.