KIF11

kinesin family member 11

Summary

This gene encodes a motor protein that belongs to the kinesin-like protein family. Members of this protein family are known to be involved in various kinds of spindle dynamics. The function of this gene product includes chromosome positioning, centrosome separation and establishing a bipolar spindle during cell mitosis. [provided by RefSeq, Jul 2008]

Known Variants665 total

rsidPosition (GRCh37)AllelesClassClinVar
rs1118708310:94,352,505A/T—benign
rs1118708410:94,352,618C/T—benign
rs7415165910:94,352,736A/G—benign
rs7415166010:94,352,747C/G—likely benign
rs229774310:94,352,823C/G—benign
rs11319769210:94,352,918A/G—benign
rs249245401210:94,353,133A/G—pathogenic
rs155485813010:94,353,134T/C—pathogenic
rs134020617710:94,353,137C/T—uncertain significance
rs77676609810:94,353,141G/A—likely benign
rs76484473410:94,353,158C/G—uncertain significance
rs103542252410:94,353,162G/A—likely benign
rs120067771710:94,353,173A/C—likely benign
rs116932028010:94,353,177G/A—likely benign
rs137212139110:94,353,201G/C—likely benign
rs213589254410:94,353,208A/G—pathogenic
rs156470025910:94,353,209G/T—uncertain significance
rs105752473610:94,353,210G/A—pathogenic
rs20018819510:94,353,214G/C—likely benign
rs249245426610:94,353,216A/C—likely benign
rs98913669810:94,353,220G/A—likely benign
rs36781058310:94,353,227A/G—likely benign
rs126537136910:94,353,229G/T—likely benign
rs1225643510:94,353,278G/T—benign
rs1181833210:94,353,438T/C—benign
rs1224268110:94,365,693G/A—benign
rs1225727910:94,365,741A/G—benign
rs20098056410:94,366,003T/C—likely benign
rs77326005810:94,366,008A/G—likely benign
rs76591008310:94,366,019T/C—uncertain significance
rs249247553410:94,366,022A/G—likely benign
rs249247555910:94,366,033T/A—likely pathogenic
rs77393421110:94,366,041C/T—uncertain significance
rs128206442410:94,366,042G/A—likely benign
rs75917050410:94,366,049T/C—benign
rs19969883710:94,366,052C/T—likely benign
rs76578593710:94,366,058T/C—likely benign
rs158959019910:94,366,061A/G—likely benign
rs56113324510:94,366,062A/G—uncertain significance
rs184443033310:94,366,064A/G—uncertain significance
rs145840720210:94,366,065G/C—uncertain significance
rs37313596010:94,366,067A/G—likely benign
rs184443048810:94,366,075A/G—uncertain significance
rs156470412110:94,366,076T/A—conflicting classifications of pathogenicity
rs122748040010:94,366,083C/T—pathogenic
rs37603237410:94,366,092G/C—likely benign
rs184443067510:94,366,095A/G—uncertain significance
rs184443070510:94,366,096G/A—uncertain significance
rs213590055810:94,366,101C/T—pathogenic
rs76968027610:94,366,108G/C—uncertain significance
rs77792320110:94,366,118T/C—likely benign
rs129816667110:94,366,123A/T—uncertain significance
rs18404928310:94,366,124G/A—likely benign
rs77036211210:94,366,130A/G—likely benign
rs20041046810:94,366,137A/G—conflicting classifications of pathogenicity
rs249247586710:94,366,148T/C—likely benign
rs79605214410:94,366,149G/A—uncertain significance
rs213590059010:94,366,150A/C—uncertain significance
rs213590059410:94,366,158A/G—uncertain significance
rs249247588510:94,366,160A/G—uncertain significance
rs77510515910:94,366,162A/G—likely benign
rs37296111510:94,366,167G/T—likely benign
rs76556974010:94,366,168C/A—likely benign
rs37596298510:94,366,170A/G—likely benign
rs8025027810:94,366,213A/G—likely benign
rs75603281210:94,366,360T/A—likely benign
rs37101014610:94,366,370C/T—likely benign
rs77086156610:94,366,371G/A—likely benign
rs18202379210:94,366,381T/C—likely benign
rs36919651710:94,366,385G/A—likely benign
rs77014518010:94,366,391A/G—uncertain significance
rs119053059210:94,366,394A/G—uncertain significance
rs166134930310:94,366,402T/G—uncertain significance
rs184443390910:94,366,403G/C—uncertain significance
rs76338855210:94,366,406G/A—uncertain significance
rs18491053610:94,366,411C/T—likely benign
rs106479673810:94,366,412C/Tstop gainedpathogenic
rs119734094010:94,366,413G/A—uncertain significance
rs75975576210:94,366,429A/G—benign
rs184443427210:94,366,430A/C—uncertain significance
rs155485934410:94,366,439G/T—pathogenic
rs213590079110:94,366,442G/A—uncertain significance
rs52756287210:94,366,474G/A—pathogenic
rs213590081210:94,366,478G/A—uncertain significance
rs184443462710:94,366,479T/C—uncertain significance
rs125759364010:94,366,485G/T—likely benign
rs20141472510:94,366,486G/A—benign
rs75698468010:94,366,487T/A—conflicting classifications of pathogenicity
rs1224466010:94,366,598G/A—benign
rs1224457310:94,366,625C/T—benign
rs1224480910:94,366,835G/T—benign
rs1225947410:94,366,898A/G—benign
rs138971188110:94,366,903T/G—likely benign
rs249247779410:94,366,905A/C—likely benign
rs76443039110:94,366,919T/C—likely benign
rs249247784910:94,366,933C/G—uncertain significance
rs130704179210:94,366,949A/T—likely benign
rs158959072310:94,366,956G/T—uncertain significance
rs37670691510:94,366,979G/A—likely benign
rs158959073710:94,366,988G/A—pathogenic

Showing 100 of 665 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.