DNAH17

dynein axonemal heavy chain 17

Summary

Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. DNAH17 is a heavy chain associated with axonemal dynein (Milisav and Affara, 1998 [PubMed 9545504]).[supplied by OMIM, Mar 2008]

Known Variants887 total

rsidPosition (GRCh37)AllelesClassClinVar
rs7290332317:76,419,882G/A—benign
rs14142423217:76,420,011G/A—likely benign
rs14324680617:76,420,030G/A—uncertain significance
rs19966966017:76,420,046T/C—uncertain significance
rs77531066217:76,420,064A/G—uncertain significance
rs11734056817:76,420,080G/A—likely benign
rs7802328817:76,420,085T/C—benign
rs14298365017:76,420,133G/A—uncertain significance
rs118769236517:76,420,157A/T—uncertain significance
rs76236412117:76,420,160T/C—uncertain significance
rs14574239717:76,420,192C/T—uncertain significance
rs19167194517:76,420,193G/A—likely benign
rs1294270317:76,420,373G/A—benign
rs5597397317:76,420,393G/A—benign
rs5624629617:76,420,437T/A—benign
rs113454117:76,421,443G/A—benign
rs3542292617:76,421,464C/T—benign
rs3611927517:76,421,467A/G—benign
rs76396938117:76,421,469G/A—uncertain significance
rs138557711917:76,421,472C/T—uncertain significance
rs52817638217:76,421,486C/T—uncertain significance
rs14717913417:76,421,503C/T—likely benign
rs14244172017:76,421,505C/T—uncertain significance
rs57005699517:76,421,531G/A—uncertain significance
rs14037896217:76,421,535A/G—benign
rs76600293717:76,421,543T/C—uncertain significance
rs78076409017:76,421,551C/T—uncertain significance
rs75237324017:76,421,552A/G—uncertain significance
rs75759927317:76,421,553T/C—uncertain significance
rs14739619217:76,421,564A/G—uncertain significance
rs100414875217:76,421,570G/A—uncertain significance
rs77912993717:76,421,611G/A—likely benign
rs14277288017:76,421,626A/C—likely benign
rs806952117:76,421,709C/A—benign
rs806968917:76,421,795C/G—benign
rs806954617:76,421,813A/G—benign
rs7291488217:76,422,372T/C—benign
rs496918817:76,422,473T/C—benign
rs7400131417:76,422,531C/A—benign
rs37596835617:76,422,545C/T—uncertain significance
rs14127973517:76,422,562G/A—likely benign
rs53546770017:76,422,571C/T—likely benign
rs37141865217:76,422,580C/T—uncertain significance
rs139531503817:76,422,584A/G—uncertain significance
rs3597325717:76,422,599C/T—likely benign
rs37600286017:76,422,600G/A—uncertain significance
rs76217947117:76,422,621C/T—uncertain significance
rs11201799917:76,422,643G/T—likely benign
rs54422636917:76,422,660C/T—uncertain significance
rs13832604717:76,422,661G/A—likely benign
rs76198170317:76,422,675G/C—uncertain significance
rs7291488317:76,422,815A/G—benign
rs7291488517:76,422,872A/C—benign
rs7291488717:76,422,903A/G—benign
rs7291489117:76,422,933G/C—benign
rs56267854517:76,423,038C/T—uncertain significance
rs36974770117:76,423,041C/T—uncertain significance
rs96766630817:76,423,048C/T—uncertain significance
rs3578207817:76,423,058G/A—benign
rs78051510317:76,423,059A/T—uncertain significance
rs227161317:76,423,097A/G—benign
rs75633441717:76,423,113G/A—uncertain significance
rs3508109317:76,423,125A/G—benign
rs37275595617:76,423,134G/C—conflicting classifications of pathogenicity
rs76053319717:76,423,137A/T—uncertain significance
rs320903017:76,423,151C/T—benign
rs75990519717:76,423,171C/T—uncertain significance
rs7291489317:76,423,358T/C—benign
rs11579364217:76,424,218C/Tdownstream gene variant—
rs11624679217:76,424,219A/Gdownstream gene variant—
rs65180617:76,424,482A/G—benign
rs69167417:76,424,502C/G—benign
rs14653866417:76,424,614C/T—uncertain significance
rs3559790217:76,424,616C/A—uncertain significance
rs76194781617:76,424,617G/A—uncertain significance
rs74766622617:76,424,646G/A—uncertain significance
rs14681282117:76,424,694G/A—uncertain significance
rs55186687317:76,424,767C/T—uncertain significance
rs69111317:76,424,942T/C—benign
rs69109417:76,425,176G/A—benign
rs6174217817:76,425,218G/C—benign
rs37043549217:76,425,223G/C—uncertain significance
rs251129474917:76,425,245A/C—uncertain significance
rs123820879017:76,425,262C/T—uncertain significance
rs7467929917:76,425,268C/T—benign
rs14275836517:76,425,269G/A—uncertain significance
rs14400127917:76,425,297T/C—uncertain significance
rs14228818417:76,425,305C/T—uncertain significance
rs251129497417:76,425,314C/G—uncertain significance
rs75086474717:76,425,362C/T—uncertain significance
rs37689267117:76,425,363G/A—uncertain significance
rs7866231517:76,425,400G/A—benign
rs66646317:76,425,480A/T—benign
rs170975217:76,425,490T/C—benign
rs170975117:76,425,491G/A—benign
rs196445017:76,425,570T/C—benign
rs7138595917:76,425,582A/G—benign
rs37019689817:76,430,119G/A—likely benign
rs988939717:76,430,127G/A—likely benign
rs52968507317:76,430,166C/T—uncertain significance

Showing 100 of 887 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.