MYO19

myosin XIX

Summary

Enables ATP hydrolysis activity and actin binding activity. Involved in regulation of cytokinesis and regulation of mitochondrial fission. Acts upstream of or within mitochondrion migration along actin filament. Located in cytosol and mitochondrial outer membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants87 total

rsidPosition (GRCh37)AllelesClassClinVar
rs77606053617:34,852,099C/T—uncertain significance
rs57194793417:34,852,127C/T—uncertain significance
rs250873968317:34,852,146T/C—likely benign
rs76948244017:34,852,184G/A—uncertain significance
rs37481855117:34,852,213C/T—uncertain significance
rs119435787117:34,854,131C/T—likely benign
rs76619654117:34,854,132G/A—uncertain significance
rs250887471017:34,854,154C/T—uncertain significance
rs207119505117:34,854,171C/G—uncertain significance
rs74734179017:34,854,180C/T—uncertain significance
rs77549398117:34,854,199G/A—uncertain significance
rs96891262317:34,854,274G/T—uncertain significance
rs74934401317:34,854,315G/A—uncertain significance
rs11303640017:34,854,377T/C—benign
rs37464104717:34,854,379T/C—uncertain significance
rs127852825717:34,854,391A/G—uncertain significance
rs137869889017:34,854,397T/C—uncertain significance
rs37715550017:34,854,956G/C—uncertain significance
rs37062908617:34,854,959G/A—uncertain significance
rs37449695517:34,856,703G/A—uncertain significance
rs250908571317:34,856,724G/A—uncertain significance
rs147609876717:34,856,739C/T—uncertain significance
rs77850987717:34,856,750C/T—uncertain significance
rs207147626517:34,856,754C/G—uncertain significance
rs57003238217:34,856,771C/T—likely benign
rs74545740517:34,856,778G/A—uncertain significance
rs250909853617:34,856,959G/T—uncertain significance
rs74972816217:34,856,973G/A—uncertain significance
rs36858755817:34,856,982G/A—uncertain significance
rs75557621217:34,857,040G/A—uncertain significance
rs250910503917:34,857,069C/T—uncertain significance
rs76223393117:34,859,791G/A—uncertain significance
rs19203379217:34,859,817T/C—uncertain significance
rs76420127717:34,861,189G/A—uncertain significance
rs76699449717:34,862,384G/C—uncertain significance
rs122702690617:34,862,407G/A—uncertain significance
rs77321567117:34,862,803T/A—uncertain significance
rs75888319417:34,862,854T/C—uncertain significance
rs74910680917:34,862,879G/A—uncertain significance
rs95761251117:34,862,933G/A—uncertain significance
rs37312092017:34,862,951C/T—uncertain significance
rs36976849817:34,862,972G/A—uncertain significance
rs90230736017:34,863,278A/G—uncertain significance
rs721734617:34,863,282G/C—uncertain significance
rs57389953317:34,863,344T/C—uncertain significance
rs20111372417:34,863,691T/C—uncertain significance
rs37596244917:34,863,695C/T—uncertain significance
rs78070301417:34,863,748T/C—uncertain significance
rs37004226617:34,864,922C/T—uncertain significance
rs250950871317:34,864,958C/G—uncertain significance
rs77102401017:34,866,593G/C—uncertain significance
rs20206571017:34,866,636C/T—likely benign
rs74599402017:34,866,640C/T—uncertain significance
rs207227310417:34,866,675G/C—uncertain significance
rs19997803917:34,866,690A/T—uncertain significance
rs101422088717:34,866,712C/A—uncertain significance
rs20072883317:34,866,718C/T—uncertain significance
rs74804833917:34,866,746C/A—uncertain significance
rs115955019517:34,867,221G/A—likely benign
rs75403430917:34,867,236G/A—uncertain significance
rs250968552517:34,869,516C/A—uncertain significance
rs250975925017:34,871,711C/T—uncertain significance
rs6174536417:34,871,819G/A—benign
rs76389082717:34,871,820C/T—uncertain significance
rs18492030717:34,878,288G/Aintron variant—
rs250999492017:34,881,072C/T—uncertain significance
rs37617762217:34,881,091T/C—uncertain significance
rs250999613217:34,881,105G/T—uncertain significance
rs37060177217:34,881,119C/G—uncertain significance
rs36913553617:34,881,163G/A—uncertain significance
rs241119217:34,882,998A/Tintron variant—
rs76948321817:34,883,419T/C—uncertain significance
rs20020303617:34,883,438G/C—uncertain significance
rs77873371617:34,883,482T/C—uncertain significance
rs74760733117:34,883,488T/A—uncertain significance
rs77694941117:34,883,504T/C—uncertain significance
rs251007286917:34,883,913G/A—uncertain significance
rs207359355517:34,883,918A/G—uncertain significance
rs77347978917:34,883,922T/A—uncertain significance
rs76530276617:34,883,928G/A—uncertain significance
rs93580216117:34,883,942T/G—uncertain significance
rs37206390217:34,883,979C/A—uncertain significance
rs37268323917:34,884,017G/A—likely benign
rs3598924917:34,884,149T/A——
rs58777773317:34,893,161A/Gmissense variantpathogenic
rs20002425317:34,893,449A/Gmissense variantpathogenic
rs1126377017:34,896,877G/C——

Gene information from NCBI Gene. Variant classifications from ClinVar.