TACC2

transforming acidic coiled-coil containing protein 2

Summary

Transforming acidic coiled-coil proteins are a conserved family of centrosome- and microtubule-interacting proteins that are implicated in cancer. This gene encodes a protein that concentrates at centrosomes throughout the cell cycle. This gene lies within a chromosomal region associated with tumorigenesis. Expression of this gene is induced by erythropoietin and is thought to affect the progression of breast tumors. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Known Variants212 total

rsidPosition (GRCh37)AllelesClassClinVar
rs75328907310:123,809,972C/T—uncertain significance
rs37597360810:123,810,001A/G—uncertain significance
rs20069189510:123,810,043C/T—uncertain significance
rs132063140410:123,810,050A/T—uncertain significance
rs13859700010:123,842,164T/C—uncertain significance
rs254605003510:123,842,197C/T—uncertain significance
rs74825106510:123,842,238C/G—uncertain significance
rs76134852810:123,842,281G/A—uncertain significance
rs77856283610:123,842,340T/A—uncertain significance
rs159180309910:123,842,341C/T—uncertain significance
rs19967387310:123,842,352T/A—uncertain significance
rs14745835210:123,842,364C/G—uncertain significance
rs37696266610:123,842,368C/T—uncertain significance
rs75594038310:123,842,376T/G—uncertain significance
rs90769383810:123,842,425C/G—uncertain significance
rs134168418110:123,842,439C/G—uncertain significance
rs7814900310:123,842,467C/T—benign
rs77540205510:123,842,718C/A—uncertain significance
rs15121856610:123,842,755A/C—likely benign
rs15058377110:123,842,902C/T—likely benign
rs76247971810:123,843,129G/A—uncertain significance
rs254606636910:123,843,186G/C—uncertain significance
rs76225059410:123,843,211G/C—uncertain significance
rs76649127110:123,843,234C/A—uncertain significance
rs20085560410:123,843,257G/C—likely benign
rs57692237610:123,843,265A/G—uncertain significance
rs76716917510:123,843,397T/C—likely benign
rs13948221910:123,843,411G/C—uncertain significance
rs148130998810:123,843,429G/T—uncertain significance
rs77009146110:123,843,442G/A—uncertain significance
rs14890446710:123,843,523C/T—likely benign
rs76368167010:123,843,622C/T—uncertain significance
rs75687579210:123,843,634G/A—uncertain significance
rs142692292610:123,843,663A/G—uncertain significance
rs54863505510:123,843,664C/T—uncertain significance
rs13867519310:123,843,665G/A—likely benign
rs254607382010:123,843,742C/G—uncertain significance
rs708377610:123,843,775A/G—conflicting classifications of pathogenicity
rs14186073810:123,843,778G/T—uncertain significance
rs76641552310:123,843,786C/T—uncertain significance
rs145262244110:123,843,802G/A—uncertain significance
rs75857506410:123,843,832G/A—uncertain significance
rs76865101010:123,843,868C/T—likely benign
rs14452598210:123,843,874G/A—conflicting classifications of pathogenicity
rs11389307210:123,843,922C/T—likely benign
rs86795857210:123,844,020G/T—uncertain significance
rs14863768010:123,844,036C/G—uncertain significance
rs14209109410:123,844,065G/A—conflicting classifications of pathogenicity
rs37111806210:123,844,076C/G—uncertain significance
rs254607862810:123,844,080G/A—uncertain significance
rs15114633210:123,844,130A/C—uncertain significance
rs14763596010:123,844,272G/A—uncertain significance
rs76997213110:123,844,299C/A—uncertain significance
rs104813724910:123,844,362C/G—likely benign
rs78163329410:123,844,396C/T—uncertain significance
rs36849678110:123,844,398G/A—likely benign
rs75647442510:123,844,500C/G—uncertain significance
rs77083594810:123,844,528A/C—uncertain significance
rs77394790110:123,844,545G/A—likely benign
rs75854351210:123,844,570C/T—uncertain significance
rs127010008110:123,844,630C/G—uncertain significance
rs254608707910:123,844,650G/A—uncertain significance
rs207996365110:123,844,689G/A—uncertain significance
rs36900678910:123,844,710T/A—uncertain significance
rs142234723910:123,844,735A/G—uncertain significance
rs57350937110:123,844,825C/T—likely benign
rs14219414610:123,844,857C/T—conflicting classifications of pathogenicity
rs74661060310:123,844,990A/C—uncertain significance
rs36938622910:123,845,002C/A—likely benign
rs76205453410:123,845,035A/G—uncertain significance
rs144520981810:123,845,091C/T—likely benign
rs6175307310:123,845,115G/A—likely benign
rs254609420810:123,845,142G/A—uncertain significance
rs14337788610:123,845,149C/T—likely benign
rs77108593410:123,845,296C/T—uncertain significance
rs75319412910:123,845,332C/G—benign
rs92574906010:123,845,383A/G—uncertain significance
rs147784525010:123,845,388G/A—uncertain significance
rs75923643510:123,845,406G/A—uncertain significance
rs254609938810:123,845,475A/G—likely benign
rs77511486110:123,845,519C/T—likely benign
rs54303962810:123,845,528A/C—uncertain significance
rs14682885310:123,845,659C/T—uncertain significance
rs37498024910:123,845,664C/T—uncertain significance
rs75711566810:123,845,680T/G—uncertain significance
rs78122697810:123,845,694C/T—uncertain significance
rs254610644010:123,845,830G/T—uncertain significance
rs77155039710:123,845,839C/T—likely benign
rs7772285410:123,845,937C/A—benign
rs208010359310:123,845,949G/A—uncertain significance
rs14367852310:123,845,976G/C—conflicting classifications of pathogenicity
rs75376902110:123,845,995C/T—uncertain significance
rs57437684910:123,846,006C/T—uncertain significance
rs90858017310:123,846,007G/A—uncertain significance
rs14113744410:123,846,060A/G—uncertain significance
rs254611210510:123,846,126G/A—uncertain significance
rs14952458410:123,846,133G/A—uncertain significance
rs20170946010:123,846,252G/A—likely benign
rs75424235610:123,846,276C/T—uncertain significance
rs13871256510:123,846,478C/T—likely benign

Showing 100 of 212 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.