DNAH9

dynein axonemal heavy chain 9

Summary

This gene encodes the heavy chain subunit of axonemal dynein, a large multi-subunit molecular motor. Axonemal dynein attaches to microtubules and hydrolyzes ATP to mediate the movement of cilia and flagella. The gene expresses at least two transcript variants; additional variants have been described, but their full length nature has not been determined. [provided by RefSeq, Jul 2008]

Known Variants1,593 total

rsidPosition (GRCh37)AllelesClassClinVar
rs91750717:11,501,730C/A—benign
rs1260401317:11,501,814C/T—benign
rs135992516217:11,501,818G/A—uncertain significance
rs55542916317:11,501,822C/T—uncertain significance
rs145962742417:11,501,830G/A—likely benign
rs75193421217:11,501,839C/T—likely benign
rs75546509517:11,501,842G/T—likely benign
rs78171555017:11,501,845C/T—likely benign
rs18601951317:11,501,854G/C—uncertain significance
rs37771589517:11,501,857C/G—conflicting classifications of pathogenicity
rs92562455317:11,501,860G/A—likely benign
rs93625818117:11,501,875C/A—likely benign
rs132709811317:11,501,876G/T—uncertain significance
rs53822139017:11,501,884A/C—benign
rs77422766017:11,501,885C/T—pathogenic
rs75945859417:11,501,886G/A—uncertain significance
rs54006897417:11,501,887A/C—likely benign
rs77553560517:11,501,889T/A—uncertain significance
rs135032138417:11,501,914C/T—likely benign
rs97892413617:11,501,915A/G—uncertain significance
rs254417508817:11,501,920C/G—uncertain significance
rs148982374317:11,501,924C/T—uncertain significance
rs124713736617:11,501,928C/T—uncertain significance
rs102808688517:11,501,939G/T—uncertain significance
rs126528462417:11,501,968G/C—uncertain significance
rs126193325117:11,501,971G/C—likely benign
rs122064773017:11,501,973A/C—uncertain significance
rs254417536317:11,501,992C/G—uncertain significance
rs7613516717:11,501,995G/C—likely benign
rs75537734117:11,501,996G/C—uncertain significance
rs149052855917:11,502,002G/C—uncertain significance
rs52734316217:11,502,016G/A—likely benign
rs2857021517:11,502,023C/T—benign
rs254417558417:11,502,028G/C—likely benign
rs86646393817:11,502,029C/T—likely benign
rs148426807917:11,502,035G/A—uncertain significance
rs97717522317:11,502,036T/G—uncertain significance
rs92562354617:11,502,043C/G—likely benign
rs145026080917:11,502,049C/T—likely benign
rs101425014917:11,502,050A/G—uncertain significance
rs74933800817:11,502,053G/T—uncertain significance
rs254417583917:11,502,060C/T—uncertain significance
rs37577561917:11,502,065C/T—conflicting classifications of pathogenicity
rs76299016517:11,502,068C/T—uncertain significance
rs142819599817:11,502,070C/T—likely benign
rs139932889817:11,502,072G/C—uncertain significance
rs117386040417:11,502,074C/T—likely benign
rs1186762517:11,502,076G/A—benign
rs77203944517:11,502,086C/T—uncertain significance
rs129931709217:11,502,087C/G—uncertain significance
rs2850796217:11,502,121T/C—likely benign
rs37378459117:11,502,123T/C—conflicting classifications of pathogenicity
rs20055425817:11,502,124C/A—benign
rs254417630517:11,502,128C/G—uncertain significance
rs75658202417:11,502,129G/A—uncertain significance
rs76456375517:11,502,130C/G—likely benign
rs75394475317:11,502,132C/T—uncertain significance
rs75744945317:11,502,137C/T—uncertain significance
rs75872457817:11,502,139C/T—likely benign
rs74683824817:11,502,152C/T—uncertain significance
rs131227799517:11,502,154C/T—likely benign
rs98582222117:11,502,179T/G—uncertain significance
rs128121128817:11,502,188C/T—likely benign
rs74763694617:11,502,190G/T—likely benign
rs76924727417:11,502,191C/T—uncertain significance
rs133755877117:11,502,193C/T—likely benign
rs76463477217:11,502,203C/T—likely benign
rs53408030917:11,502,209C/G—likely benign
rs122812285017:11,502,210A/G—uncertain significance
rs76537000017:11,502,217C/G—likely benign
rs75053630117:11,502,218G/A—uncertain significance
rs75863654117:11,502,221C/G—uncertain significance
rs78020788917:11,502,228C/T—uncertain significance
rs75477750817:11,502,240T/G—likely benign
rs207232357717:11,502,252C/G—likely benign
rs7980745317:11,502,259G/C—benign
rs807956617:11,502,403G/C—benign
rs7838961317:11,502,566T/Cregulatory region variant—
rs989630717:11,511,411C/T—benign
rs479215617:11,511,412A/G—benign
rs75525788117:11,511,427C/T—benign
rs14928723317:11,511,432C/T—benign
rs77775848217:11,511,441T/C—likely benign
rs1107802217:11,511,457C/T—benign
rs254419982517:11,511,474A/C—uncertain significance
rs1759963917:11,511,480G/A—benign
rs11201710017:11,511,484A/C—likely benign
rs254419988617:11,511,486A/C—uncertain significance
rs13794259617:11,511,497A/G—uncertain significance
rs103731778817:11,511,514C/G—likely benign
rs14947579017:11,511,520G/A—likely benign
rs37617263517:11,511,523C/T—likely benign
rs75725198817:11,511,524G/A—uncertain significance
rs130675171317:11,511,530A/T—uncertain significance
rs254420006217:11,511,532C/T—likely benign
rs254420012917:11,511,546T/A—uncertain significance
rs20077666017:11,511,563C/G—uncertain significance
rs55558837717:11,511,641G/C—uncertain significance
rs77133324317:11,511,652G/T—likely benign
rs219107217:11,513,661C/T—benign

Showing 100 of 1,593 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.