DIP2C

DIP2 acetate--CoA ligase C (putative)

Summary

This gene encodes a member of the disco-interacting protein homolog 2 family. The protein shares strong similarity with a Drosophila protein which interacts with the transcription factor disco and is expressed in the nervous system. [provided by RefSeq, Oct 2008]

Known Variants641 total

rsidPosition (GRCh37)AllelesClassClinVar
rs75057647610:323,271G/A—likely benign
rs75621316110:323,277G/C—likely benign
rs374030410:323,283A/G—benign
rs74858437710:323,304T/C—likely benign
rs77251175310:323,316G/A—likely benign
rs195457016210:323,321G/A—conflicting classifications of pathogenicity
rs77625508410:323,343C/A—likely benign
rs77534713310:323,363T/C—uncertain significance
rs76273793810:323,366C/T—uncertain significance
rs14037582610:323,367G/A—benign
rs15038106510:323,369C/T—uncertain significance
rs13822781810:323,370G/A—likely benign
rs76430236510:323,371A/C—uncertain significance
rs14360775810:323,382G/A—likely benign
rs52862873910:323,394G/A—likely benign
rs77823740310:323,397G/A—likely benign
rs195457554610:323,433C/T—likely benign
rs14108186410:323,442C/T—benign
rs141539409110:323,460T/G—uncertain significance
rs13838572010:323,463C/T—likely benign
rs14959106310:323,479A/G—uncertain significance
rs14419966810:323,499T/G—benign
rs75902623010:323,511C/G—likely benign
rs141502370310:323,521A/G—likely benign
rs37160354110:327,132C/T—likely benign
rs75766758310:327,133G/A—likely benign
rs78135801410:327,150C/T—uncertain significance
rs75077837610:327,151G/A—likely benign
rs14243840410:327,162C/T—uncertain significance
rs14638885510:327,172C/T—likely benign
rs13977373510:327,187G/A—likely benign
rs14439477810:327,189T/C—uncertain significance
rs142518151010:327,200C/T—uncertain significance
rs133210838710:327,208C/T—likely benign
rs195480564010:327,219T/C—uncertain significance
rs14487417210:327,226G/A—benign
rs53313677210:327,238T/C—likely benign
rs156449979310:327,240C/T—uncertain significance
rs117051328110:327,243C/T—uncertain significance
rs76654251810:327,244G/C—uncertain significance
rs195480752310:327,263T/G—uncertain significance
rs7265303010:329,192C/A—likely benign
rs57402621310:329,193C/T—likely benign
rs20161632310:329,205C/A—benign
rs75989512110:329,209C/T—uncertain significance
rs100849175410:329,225T/C—likely benign
rs57314230510:329,231C/A—uncertain significance
rs254020942210:329,242G/A—uncertain significance
rs76360880010:329,258G/T—likely benign
rs75108855610:329,259C/G—uncertain significance
rs75729663210:329,261T/C—likely benign
rs53448106710:329,266G/A—uncertain significance
rs195493970510:329,297T/G—likely benign
rs20015828210:329,338C/T—conflicting classifications of pathogenicity
rs37745027510:329,339G/A—likely benign
rs14969927710:329,344T/C—conflicting classifications of pathogenicity
rs14544366710:329,357G/A—likely benign
rs36833558110:329,392A/G—likely benign
rs37194028610:329,395G/A—likely benign
rs254021030010:329,397A/G—likely benign
rs195494354310:329,400G/A—likely benign
rs77796758010:329,404T/G—likely benign
rs37718101910:332,198G/A—likely benign
rs228868010:332,199A/G—benign
rs37731267410:332,202A/G—likely benign
rs11345276910:332,207A/G—benign
rs18698409410:332,231C/T—likely benign
rs254022256510:332,234C/G—likely benign
rs77183056310:332,237C/T—likely benign
rs20195029310:332,252T/C—likely benign
rs254022288910:332,274A/G—uncertain significance
rs14693881010:332,279T/G—benign
rs213216795610:332,289T/C—uncertain significance
rs1715897710:332,290A/G—benign
rs254022310510:332,291T/C—uncertain significance
rs75057061310:332,298G/A—likely benign
rs123400812910:334,284C/T—likely benign
rs36991749010:334,305T/C—uncertain significance
rs37286582210:334,310C/T—likely benign
rs195526794810:334,322G/A—likely benign
rs98839523510:334,372A/G—likely benign
rs254023311610:334,376A/G—likely benign
rs37615080410:334,377G/A—likely benign
rs20066643610:355,956A/G—benign
rs74917302710:355,957G/C—likely benign
rs131402928310:355,961T/C—likely benign
rs254036019710:355,963T/A—likely benign
rs20056129610:355,976G/A—likely benign
rs254036030110:355,977T/G—uncertain significance
rs75778746210:356,000G/A—likely benign
rs76342334710:356,045A/C—likely benign
rs19090717510:370,950A/C—not provided
rs139397009510:372,933C/A—likely benign
rs14745399610:372,934G/A—benign
rs36803813710:372,936C/T—likely benign
rs37016114310:372,937G/A—likely benign
rs36848356810:372,949C/T—benign
rs76604104810:372,967C/G—likely benign
rs14764079010:372,973G/A—likely benign
rs56801299710:372,979G/A—likely benign

Showing 100 of 641 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.