TUBGCP6

tubulin gamma complex component 6

Summary

The protein encoded by this gene is part of a large multisubunit complex required for microtubule nucleation at the centrosome. [provided by RefSeq, Jul 2008]

Known Variants1,722 total

rsidPosition (GRCh37)AllelesClassClinVar
rs11312144622:50,656,034C/T—benign
rs228111622:50,656,053T/A—benign
rs203805022:50,656,096A/G—benign
rs5595521122:50,656,109C/A—benign
rs962830522:50,656,126G/A—likely benign
rs37002486922:50,656,169G/A—uncertain significance
rs76039677622:50,656,171G/A—likely benign
rs206443867022:50,656,172T/C—uncertain significance
rs14170708322:50,656,174C/T—likely benign
rs77620791622:50,656,179A/G—uncertain significance
rs206443899022:50,656,181T/G—uncertain significance
rs76216715422:50,656,185T/A—uncertain significance
rs251911859622:50,656,189G/A—likely benign
rs76582342322:50,656,190A/T—uncertain significance
rs18975780822:50,656,192G/A—likely benign
rs120531961022:50,656,194T/A—uncertain significance
rs75168580922:50,656,198G/A—likely benign
rs54095724522:50,656,199C/T—uncertain significance
rs123644147922:50,656,200G/A—uncertain significance
rs78106859722:50,656,201C/T—likely benign
rs140763494422:50,656,206G/A—likely benign
rs75283735722:50,656,207A/G—likely benign
rs214717065422:50,656,209A/G—uncertain significance
rs251911870722:50,656,221G/A—uncertain significance
rs37354180722:50,656,223G/A—uncertain significance
rs160250059822:50,656,224G/C—uncertain significance
rs251911871822:50,656,228G/A—likely benign
rs206443999722:50,656,229T/A—uncertain significance
rs15013790422:50,656,233C/T—uncertain significance
rs77180470622:50,656,234G/A—likely benign
rs77938908222:50,656,235C/T—uncertain significance
rs13860968622:50,656,236G/A—uncertain significance
rs76836654622:50,656,237G/C—uncertain significance
rs74871197922:50,656,245G/A—likely benign
rs19997680022:50,656,247T/C—uncertain significance
rs143295372822:50,656,249G/C—likely benign
rs214717075822:50,656,259G/C—uncertain significance
rs251911884122:50,656,261G/C—likely benign
rs54461955422:50,656,262G/A—likely benign
rs130947459922:50,656,267G/A—likely benign
rs20218273222:50,656,269G/T—likely benign
rs20107058222:50,656,317C/T—likely benign
rs214717091422:50,656,330G/A—likely benign
rs124666652022:50,656,331C/A—likely benign
rs75148709322:50,656,334G/A—likely benign
rs75477670522:50,656,335G/C—likely benign
rs251911929522:50,656,336G/A—likely benign
rs78087472622:50,656,338G/A—likely benign
rs134996976822:50,656,340G/T—likely benign
rs75583584922:50,656,354G/A—likely benign
rs75584109522:50,656,363G/A—likely benign
rs77041717122:50,656,364G/T—uncertain significance
rs77489111722:50,656,365A/G—uncertain significance
rs160250106222:50,656,366G/T—uncertain significance
rs74641127722:50,656,375G/T—uncertain significance
rs77244136222:50,656,378G/C—likely benign
rs77056522322:50,656,382T/G—uncertain significance
rs214717100822:50,656,383T/C—uncertain significance
rs133178145322:50,656,384G/A—likely benign
rs76428629422:50,656,385T/C—uncertain significance
rs37420424022:50,656,388G/C—conflicting classifications of pathogenicity
rs37617848122:50,656,396C/T—uncertain significance
rs75255654022:50,656,399G/A—likely benign
rs75603272122:50,656,401G/A—uncertain significance
rs214717106122:50,656,408G/A—likely benign
rs74898908322:50,656,419C/T—uncertain significance
rs75677099122:50,656,427C/T—uncertain significance
rs3538139422:50,656,428A/G—benign
rs74632000822:50,656,429C/T—likely benign
rs20172181222:50,656,430G/A—conflicting classifications of pathogenicity
rs251911977122:50,656,435C/A—likely benign
rs119351167622:50,656,437C/T—uncertain significance
rs11256956422:50,656,439G/C—uncertain significance
rs76196058222:50,656,443G/T—uncertain significance
rs160250136522:50,656,446C/G—uncertain significance
rs77317331122:50,656,449A/C—uncertain significance
rs251911991222:50,656,454T/G—uncertain significance
rs75275056922:50,656,455G/T—uncertain significance
rs206444656622:50,656,457G/A—uncertain significance
rs251911993122:50,656,459G/A—likely benign
rs14045689622:50,656,461T/C—uncertain significance
rs75348309522:50,656,462G/A—likely benign
rs75686407722:50,656,463A/T—uncertain significance
rs77842881322:50,656,466T/G—uncertain significance
rs53956820922:50,656,473G/A—uncertain significance
rs214717126222:50,656,474G/A—likely benign
rs78050533122:50,656,475A/C—uncertain significance
rs214717127322:50,656,479T/C—uncertain significance
rs14286964322:50,656,480G/C—likely benign
rs14743735022:50,656,485C/T—uncertain significance
rs78156403922:50,656,486G/A—likely benign
rs206444718722:50,656,488G/A—uncertain significance
rs74833951622:50,656,496A/T—uncertain significance
rs13983541022:50,656,507G/A—likely benign
rs76293971522:50,656,509C/T—uncertain significance
rs37728286922:50,656,510G/C—uncertain significance
rs77554671222:50,656,518C/T—uncertain significance
rs76071229222:50,656,519G/A—likely benign
rs134846694422:50,656,520G/A—uncertain significance
rs14384648822:50,656,522C/T—likely benign

Showing 100 of 1,722 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.