DNAH12

dynein axonemal heavy chain 12

Summary

Predicted to enable several functions, including ATP binding activity; ATP hydrolysis activity; and dynein intermediate chain binding activity. Predicted to be involved in microtubule-based movement. Predicted to be located in axoneme and microtubule. Predicted to be part of axonemal dynein complex. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants215 total

rsidPosition (GRCh37)AllelesClassClinVar
rs3722762163:57,327,815A/Tuncertain significance
rs3744601163:57,327,847T/Cuncertain significance
rs9145373943:57,327,858C/Tlikely benign
rs5512716803:57,327,859G/Auncertain significance
rs1479665413:57,327,862T/Cuncertain significance
rs3731300593:57,327,936C/Tuncertain significance
rs9009872503:57,327,937G/Auncertain significance
rs7736737213:57,327,975G/Auncertain significance
rs5423078063:57,327,987C/Tlikely benign
rs1140758703:57,330,409C/Tuncertain significance
rs14355094993:57,330,900A/Guncertain significance
rs14341517453:57,330,901T/Cuncertain significance
rs12097904853:57,330,954T/Cuncertain significance
rs9554961973:57,335,792C/Tuncertain significance
rs25289825943:57,335,802A/Tuncertain significance
rs40607263:57,335,876T/Cbenign
rs1995664843:57,335,909C/Tuncertain significance
rs3701347853:57,343,185A/Guncertain significance
rs9327133963:57,343,248C/Tlikely benign
rs7670373683:57,343,267C/Tuncertain significance
rs25290508813:57,343,707T/Cuncertain significance
rs20615479063:57,343,737G/Auncertain significance
rs20615503543:57,343,806G/Cuncertain significance
rs5657901003:57,344,758A/Guncertain significance
rs3706881933:57,344,805G/Alikely benign
rs2017324203:57,344,879G/Auncertain significance
rs9930190673:57,348,545G/Auncertain significance
rs5395430893:57,348,556T/Guncertain significance
rs13930995413:57,356,414A/Cuncertain significance
rs5622748303:57,356,459G/Auncertain significance
rs13714523453:57,356,486C/Guncertain significance
rs9285435123:57,357,046G/Auncertain significance
rs13355370173:57,357,082A/Tuncertain significance
rs2000750953:57,357,084G/Cuncertain significance
rs7603539973:57,357,126A/Guncertain significance
rs7534491973:57,357,164C/Auncertain significance
rs25291434163:57,357,171C/Tuncertain significance
rs3718946383:57,357,207A/Guncertain significance
rs9025918223:57,357,235T/Cuncertain significance
rs9014311793:57,357,511G/Auncertain significance
rs626212333:57,357,514C/Tuncertain significance
rs2007035883:57,357,527C/Tuncertain significance
rs7799467023:57,357,620T/Cuncertain significance
rs25291492033:57,357,638C/Tuncertain significance
rs12088677193:57,368,512C/Tuncertain significance
rs9960515023:57,368,516G/Cuncertain significance
rs12041578443:57,368,614T/Cuncertain significance
rs12078807153:57,368,835C/Guncertain significance
rs7725917383:57,368,844G/Auncertain significance
rs3709487183:57,368,883G/Auncertain significance
rs14509681883:57,368,939A/Guncertain significance
rs5303586443:57,368,958C/Guncertain significance
rs10030249963:57,368,964T/Cuncertain significance
rs7822763143:57,386,145T/Auncertain significance
rs120539753:57,386,148C/Gbenign
rs10022067923:57,386,161T/Cuncertain significance
rs5528814773:57,386,189A/Guncertain significance
rs14497608773:57,386,219A/Guncertain significance
rs9399276933:57,386,249T/Guncertain significance
rs64458733:57,388,114C/Tbenign
rs13633149393:57,389,073T/Cuncertain significance
rs7825198253:57,390,752C/Guncertain significance
rs15536808963:57,391,433A/Cuncertain significance
rs9695491103:57,391,537C/Tuncertain significance
rs7824155263:57,391,538G/Auncertain significance
rs5353782973:57,391,570C/Guncertain significance
rs3691485613:57,391,592G/Auncertain significance
rs13693859193:57,391,601G/Auncertain significance
rs7457751893:57,394,012T/Cuncertain significance
rs20641010503:57,394,087C/Guncertain significance
rs5464683443:57,394,102T/Cuncertain significance
rs14185964123:57,394,107A/Guncertain significance
rs20641021173:57,394,111T/Cuncertain significance
rs19162843:57,394,766T/A
rs98531133:57,397,738T/C
rs14884568923:57,399,483A/Cuncertain significance
rs7821837793:57,399,497C/Tuncertain significance
rs7822204983:57,399,608C/Tuncertain significance
rs8939600873:57,399,632A/Guncertain significance
rs7817309423:57,401,167C/Tuncertain significance
rs7657590403:57,401,212C/Tuncertain significance
rs13469800973:57,401,254A/Guncertain significance
rs9217528863:57,401,269T/Cuncertain significance
rs7810889083:57,405,127G/Auncertain significance
rs7702497333:57,405,145A/Guncertain significance
rs7497352663:57,405,178T/Auncertain significance
rs25298379683:57,405,223A/Guncertain significance
rs13584803243:57,407,261T/Cuncertain significance
rs11609732283:57,407,313G/Auncertain significance
rs2002494013:57,407,327T/Auncertain significance
rs10013948193:57,407,330T/Auncertain significance
rs12564121923:57,407,373G/Auncertain significance
rs25298580453:57,407,420A/Guncertain significance
rs46819823:57,414,071G/Abenign
rs177930143:57,414,097T/Abenign
rs9190912643:57,414,120A/Cuncertain significance
rs25299210263:57,414,397A/Guncertain significance
rs7596871783:57,414,428C/Tuncertain significance
rs44629373:57,414,434A/Gbenign
rs14681170783:57,414,451G/Auncertain significance

Showing 100 of 215 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.