DNAJC17

DnaJ heat shock protein family (Hsp40) member C17

Summary

Predicted to enable RNA binding activity. Predicted to be involved in spliceosomal complex disassembly. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Predicted to be located in cytoplasm and nucleus. Predicted to be part of spliceosomal complex. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants161 total

rsidPosition (GRCh37)AllelesClassClinVar
rs104198897215:41,060,138C/A—uncertain significance
rs76078727415:41,060,141C/T—likely benign
rs77656945415:41,060,143T/C—uncertain significance
rs188899370215:41,060,144A/G—likely benign
rs76239503315:41,060,149G/C—uncertain significance
rs14427628615:41,060,152C/T—uncertain significance
rs20101845215:41,060,156C/T—likely benign
rs250464582415:41,060,161C/T—uncertain significance
rs75323353615:41,060,176G/C—uncertain significance
rs250464591415:41,060,183C/A—likely benign
rs74577083515:41,060,190T/G—uncertain significance
rs250464594815:41,060,194G/A—uncertain significance
rs14225153615:41,060,197C/G—uncertain significance
rs74732419815:41,060,198G/T—likely benign
rs15132752015:41,060,201C/T—likely benign
rs14060371515:41,060,221T/C—likely benign
rs77375499515:41,060,228G/A—likely benign
rs117989933315:41,060,235T/G—uncertain significance
rs91742728115:41,060,246T/G—likely benign
rs76679156015:41,060,249C/T—likely benign
rs129568394915:41,060,256G/A—uncertain significance
rs76360850615:41,060,259C/A—uncertain significance
rs36889783315:41,060,265C/T—likely benign
rs159606945515:41,060,266G/C—likely benign
rs250464625515:41,060,270A/G—likely benign
rs130374999115:41,060,276G/A—likely benign
rs57048674815:41,061,642C/T——
rs37638031915:41,065,907C/A—likely benign
rs75885249715:41,065,911G/A—likely benign
rs74749476915:41,065,914T/C—likely benign
rs74889275815:41,065,946G/A—likely benign
rs13846795615:41,065,947C/T—uncertain significance
rs74534578015:41,065,948G/A—uncertain significance
rs37125933315:41,065,970T/C—likely benign
rs13797482215:41,066,008G/C—uncertain significance
rs56347452115:41,066,033C/T—likely benign
rs56872212215:41,066,053T/A—likely benign
rs91065207715:41,066,538C/T—likely benign
rs91976470115:41,066,547C/A—likely benign
rs75014569615:41,066,554C/T—uncertain significance
rs136828358015:41,066,555G/A—uncertain significance
rs188925539115:41,066,562T/C—uncertain significance
rs54803869515:41,066,564A/T—uncertain significance
rs86830665715:41,066,565C/T—uncertain significance
rs14886804215:41,066,566G/A—likely benign
rs20023310015:41,066,587A/G—likely benign
rs124765201815:41,066,591C/T—uncertain significance
rs214194790015:41,066,598T/C—uncertain significance
rs250465849115:41,066,610G/C—uncertain significance
rs104702940815:41,066,617G/T—uncertain significance
rs11748535515:41,066,625C/G—benign
rs135218787515:41,066,650G/C—likely benign
rs76747564815:41,066,651G/A—likely benign
rs250465973515:41,067,210G/A—likely benign
rs88655589515:41,067,213C/T—likely benign
rs74904825515:41,067,225C/T—uncertain significance
rs19971941315:41,067,226G/A—uncertain significance
rs75982314315:41,067,241C/T—likely benign
rs14828486815:41,067,242C/T—conflicting classifications of pathogenicity
rs14133915515:41,067,243G/A—uncertain significance
rs76125911115:41,067,252C/T—uncertain significance
rs6176305215:41,067,253G/A—benign
rs75423478815:41,067,266C/T—uncertain significance
rs250465989315:41,067,277C/T—likely benign
rs250465991515:41,067,287T/C—uncertain significance
rs146247655415:41,067,293C/T—uncertain significance
rs14573170115:41,067,324T/A—uncertain significance
rs250466089715:41,067,749A/C—uncertain significance
rs250466090415:41,067,756G/A—likely benign
rs147649176415:41,067,767C/T—uncertain significance
rs20030977215:41,067,778A/G—likely benign
rs14857056915:41,067,791T/C—uncertain significance
rs36976578415:41,068,375C/T—likely benign
rs76186923115:41,068,376G/A—likely benign
rs77988851515:41,068,401C/A—uncertain significance
rs7339852815:41,068,409C/T—benign
rs56353417815:41,068,411C/T—uncertain significance
rs74818664415:41,068,412G/A—uncertain significance
rs96095130215:41,068,413C/T—likely benign
rs74978544615:41,068,420C/A—uncertain significance
rs77471345215:41,068,421G/C—uncertain significance
rs214194935915:41,068,452C/T—likely benign
rs188931715915:41,068,457G/A—likely benign
rs54917042415:41,068,462C/T—uncertain significance
rs76287997015:41,068,463G/A—uncertain significance
rs138373659215:41,068,467A/T—likely benign
rs18613578415:41,068,483C/T—uncertain significance
rs53478977315:41,068,484G/A—uncertain significance
rs75289099515:41,068,487C/T—uncertain significance
rs14609478815:41,068,488G/A—likely benign
rs77141517015:41,068,501G/C—likely benign
rs77917094315:41,068,502G/T—likely benign
rs77253444415:41,068,504G/A—likely benign
rs188932849915:41,068,735C/T—uncertain significance
rs37385948015:41,068,745G/T—uncertain significance
rs250466278715:41,068,746C/T—likely benign
rs250466279515:41,068,750A/G—uncertain significance
rs214194963415:41,068,754T/C—uncertain significance
rs13972890315:41,068,762C/T—uncertain significance
rs188932962515:41,068,763T/C—uncertain significance

Showing 100 of 161 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.