MYO1D

myosin ID

Summary

Enables protein domain specific binding activity. Predicted to be involved in several processes, including actin filament organization; actin filament-based movement; and early endosome to recycling endosome transport. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants72 total

rsidPosition (GRCh37)AllelesClassClinVar
rs20018503417:30,821,833G/C—likely benign
rs105432548917:30,821,848G/A—uncertain significance
rs22519017:30,877,658C/A——
rs22521217:30,896,455C/G——
rs74874514817:30,932,106T/G—uncertain significance
rs97776545117:30,932,150C/T—uncertain significance
rs11598119717:30,932,176G/A—benign
rs123537293617:30,980,893T/C—uncertain significance
rs14949764217:30,980,907C/T—uncertain significance
rs138478656917:30,980,948C/G—uncertain significance
rs14617577017:30,981,593G/A—uncertain significance
rs77632041417:30,981,613C/T—uncertain significance
rs121103223217:30,986,145G/A—uncertain significance
rs721595817:30,986,166C/T—benign
rs720910617:30,986,185G/A—likely benign
rs76940518017:30,986,200C/G—uncertain significance
rs208851956217:30,986,242G/A—uncertain significance
rs117165079217:30,986,258G/C—uncertain significance
rs136183504817:30,986,323T/C—uncertain significance
rs37128607617:31,039,046C/T—uncertain significance
rs37596421517:31,039,073C/T—uncertain significance
rs37171759517:31,039,097G/T—uncertain significance
rs74827533017:31,039,208T/A—uncertain significance
rs77947715917:31,048,053T/C—uncertain significance
rs37083268317:31,048,132G/A—uncertain significance
rs75325486317:31,048,134C/T—uncertain significance
rs37520204717:31,048,141G/A—uncertain significance
rs75166208017:31,048,147C/T—uncertain significance
rs36863464617:31,048,191C/T—uncertain significance
rs14360421517:31,048,195C/T—uncertain significance
rs250860556717:31,065,356A/C—uncertain significance
rs6206843217:31,066,497A/C——
rs77262490417:31,072,244C/T—uncertain significance
rs75130238817:31,072,289C/T—uncertain significance
rs11703681817:31,075,962G/A—likely benign
rs1718329517:31,078,272C/Tintron variant—
rs37324548817:31,082,530C/T—uncertain significance
rs7874731417:31,082,588G/A—benign
rs37374828817:31,087,330C/T—uncertain significance
rs250823543217:31,087,531T/C—uncertain significance
rs14836815517:31,087,542C/A—uncertain significance
rs250823666617:31,087,569G/A—uncertain significance
rs74621030217:31,087,578T/C—uncertain significance
rs36863158017:31,087,609G/A—uncertain significance
rs75071037917:31,087,618T/G—uncertain significance
rs117225180717:31,091,916C/T—uncertain significance
rs77271847717:31,091,960C/T—uncertain significance
rs74706555117:31,092,056T/C—uncertain significance
rs156763059617:31,092,084C/T—uncertain significance
rs11638155817:31,094,688G/C—likely benign
rs36966213117:31,098,202G/C—uncertain significance
rs14072599717:31,099,821G/A—uncertain significance
rs53105786817:31,099,844T/G—uncertain significance
rs18204499317:31,102,435G/Aintron variant—
rs209016819117:31,103,007C/T—uncertain significance
rs146165120617:31,103,021T/C—uncertain significance
rs14210976817:31,103,038A/G—likely benign
rs14331444617:31,105,536C/T—likely benign
rs20087774117:31,105,600A/G—benign
rs75634583817:31,107,779G/A—uncertain significance
rs14396247917:31,107,802T/C—likely benign
rs11291605417:31,124,262C/Tintron variant—
rs136293617:31,140,714G/A——
rs7637301517:31,142,041C/Aregulatory region variant—
rs14241401617:31,149,426A/Gintron variant—
rs14429940017:31,149,524G/Tintron variant—
rs6207018317:31,164,367T/Cintron variant—
rs1778114217:31,187,216G/T——
rs77744838517:31,203,811G/A—uncertain significance
rs76417455217:31,203,820T/A—uncertain significance
rs94448852017:31,203,829G/A—uncertain significance
rs128963350217:31,203,875T/C—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.