TCF25

TCF25 ribosome quality control complex subunit

Summary

TCF25 is a member of the basic helix-loop-helix (bHLH) family of transcription factors that are important in embryonic development (Steen and Lindholm, 2008 [PubMed 18068114]).[supplied by OMIM, Sep 2008]

Known Variants72 total

rsidPosition (GRCh37)AllelesClassClinVar
rs18294891916:89,938,244C/Tupstream gene variant—
rs53837101316:89,938,349T/A——
rs126932908416:89,940,105G/C—uncertain significance
rs76057641316:89,940,109G/A—uncertain significance
rs54511821616:89,940,116G/A—uncertain significance
rs75510963816:89,940,197G/A—uncertain significance
rs102346290116:89,940,220G/A—likely benign
rs37349273016:89,940,242T/G—uncertain significance
rs76274530516:89,940,261C/G—uncertain significance
rs992588716:89,946,302A/T——
rs3599487816:89,949,033T/Cintron variant—
rs76091711916:89,949,798G/A—uncertain significance
rs145225169916:89,949,814G/C—uncertain significance
rs77367601416:89,949,871C/G—uncertain significance
rs77820866716:89,950,996G/T—uncertain significance
rs254450011916:89,951,062T/C—uncertain significance
rs76617987316:89,951,063C/T—uncertain significance
rs11273061116:89,951,460C/G——
rs14783802016:89,952,262G/A—uncertain significance
rs75101226916:89,952,294G/T—uncertain significance
rs254450467416:89,952,299A/G—uncertain significance
rs37470812316:89,952,304A/G—uncertain significance
rs74556796216:89,952,320G/A—likely benign
rs131570085116:89,952,355G/C—uncertain significance
rs11724305216:89,956,706C/Tregulatory region variant—
rs86592221916:89,958,626C/G—uncertain significance
rs76504379516:89,958,657G/A—uncertain significance
rs37183818616:89,958,680C/T—uncertain significance
rs14613510716:89,958,764G/Aregulatory region variant—
rs7825896616:89,959,888G/Aintron variant—
rs3551809616:89,961,140C/Aregulatory region variant—
rs20195117316:89,962,404C/T—uncertain significance
rs120486234816:89,962,433C/T—uncertain significance
rs74590856216:89,962,476G/A—uncertain significance
rs254453756016:89,962,481C/T—uncertain significance
rs77994830816:89,964,994T/C—uncertain significance
rs204407197516:89,965,031G/A—likely benign
rs76159616216:89,965,032C/G—uncertain significance
rs37704304216:89,965,215A/G—likely benign
rs74541785316:89,965,233C/T—uncertain significance
rs117781852416:89,965,239C/G—uncertain significance
rs7571994316:89,967,044C/T—uncertain significance
rs77787263716:89,967,119C/T—uncertain significance
rs75481540516:89,967,175C/A—uncertain significance
rs7849843916:89,967,514G/Aintron variant—
rs89365077916:89,970,528C/G—uncertain significance
rs74655487916:89,970,559G/A—uncertain significance
rs36892592016:89,970,573G/A—uncertain significance
rs121789367416:89,970,576T/G—likely benign
rs37132862816:89,970,584C/G—uncertain significance
rs75186326516:89,970,585C/T—uncertain significance
rs20196563416:89,970,601A/G—uncertain significance
rs132767985716:89,971,384T/G—uncertain significance
rs76065332916:89,971,396A/C—uncertain significance
rs37691641416:89,971,443G/A—uncertain significance
rs141606539616:89,971,459A/C—uncertain significance
rs14493728716:89,971,469C/Tsynonymous variant—
rs77295108916:89,972,622G/A—uncertain significance
rs136767148516:89,972,660G/A—uncertain significance
rs77250382516:89,972,682C/T—uncertain significance
rs36898879616:89,973,697C/T—likely benign
rs204487439116:89,973,709A/G—uncertain significance
rs54648186716:89,975,897G/A——
rs13994154516:89,977,043G/A—uncertain significance
rs74574932116:89,977,066A/G—likely benign
rs13996779516:89,977,482C/T—likely benign
rs37081681116:89,977,507G/T—uncertain significance
rs254459694216:89,977,557G/C—uncertain significance
rs75405147816:89,977,612A/T—uncertain significance
rs78054599316:89,977,620G/A—uncertain significance
rs7576332616:89,977,625G/C—likely benign
rs159740671416:89,977,631G/C—likely benign

Gene information from NCBI Gene. Variant classifications from ClinVar.