CCDC88B

coiled-coil and HOOK domain protein 88B

Summary

This gene encodes a member of the hook-related protein family. Members of this family are characterized by an N-terminal potential microtubule binding domain, a central coiled-coiled and a C-terminal Hook-related domain. The encoded protein may be involved in linking organelles to microtubules. [provided by RefSeq, Oct 2009]

Known Variants122 total

rsidPosition (GRCh37)AllelesClassClinVar
rs47977711:64,107,477T/Cregulatory region variant—
rs66374311:64,107,735G/T——
rs142839614811:64,107,745G/A—uncertain significance
rs96384597011:64,108,144G/C—uncertain significance
rs76091962411:64,108,151C/G—uncertain significance
rs75319868811:64,108,190G/A—uncertain significance
rs37509502811:64,108,221T/C—uncertain significance
rs76488874311:64,108,453T/A—uncertain significance
rs249588665311:64,108,745A/C—uncertain significance
rs249588713311:64,108,893T/C—uncertain significance
rs77279249711:64,108,936G/T—uncertain significance
rs77676585311:64,108,949G/C—uncertain significance
rs76680538011:64,109,093T/A—uncertain significance
rs56319326411:64,109,131G/T—uncertain significance
rs103601974811:64,109,168T/G—uncertain significance
rs249588833711:64,109,198G/A—uncertain significance
rs20087768211:64,109,512C/T—uncertain significance
rs78154067411:64,109,520C/T—uncertain significance
rs14846917011:64,109,545C/T—uncertain significance
rs142726044511:64,109,588G/T—uncertain significance
rs76394857111:64,109,592C/T—uncertain significance
rs249589040311:64,109,601C/T—uncertain significance
rs249589041011:64,109,602G/A—uncertain significance
rs92153609511:64,110,037G/A—uncertain significance
rs122670272911:64,110,072C/A—uncertain significance
rs213530484411:64,110,127C/G—uncertain significance
rs1160186011:64,110,422A/G——
rs76299741111:64,110,658G/A—uncertain significance
rs75772525111:64,110,669G/C—uncertain significance
rs146719234311:64,110,681G/T—uncertain significance
rs77737631711:64,110,721G/A—likely benign
rs76320047011:64,110,788G/C—uncertain significance
rs99426199111:64,110,987C/G—uncertain significance
rs137854659411:64,111,051C/T—uncertain significance
rs56198062211:64,111,298C/T—uncertain significance
rs76109819511:64,111,328G/A—uncertain significance
rs76567026111:64,111,345C/T—uncertain significance
rs133664652311:64,111,346G/A—uncertain significance
rs77107823411:64,111,508C/A—uncertain significance
rs76348174811:64,111,542C/T—uncertain significance
rs52867462811:64,111,549C/A—likely benign
rs97452030111:64,111,550C/T—uncertain significance
rs37088930611:64,111,554G/A—uncertain significance
rs76910470711:64,111,617C/T—likely benign
rs55305548011:64,111,741G/A—likely benign
rs76386843511:64,111,788C/A—uncertain significance
rs53751141811:64,111,862C/G—uncertain significance
rs20044980211:64,111,886G/A—uncertain significance
rs159128212211:64,111,899C/A—uncertain significance
rs249590018711:64,111,994G/C—uncertain significance
rs92748247711:64,112,086G/C—uncertain significance
rs14669955411:64,112,258G/A—uncertain significance
rs14026570911:64,112,303C/T—uncertain significance
rs77409099611:64,112,387C/T—uncertain significance
rs76133355211:64,112,388G/A—uncertain significance
rs19987072011:64,112,393C/T—uncertain significance
rs75848907211:64,112,445G/A—uncertain significance
rs36864496211:64,112,447G/C—uncertain significance
rs77536576411:64,112,480C/T—uncertain significance
rs76979117511:64,112,481G/A—uncertain significance
rs76024076611:64,112,493A/G—uncertain significance
rs77539410211:64,112,502G/C—uncertain significance
rs77333532411:64,112,540G/A—uncertain significance
rs74640131011:64,112,547G/A—uncertain significance
rs249590217311:64,112,550T/G—uncertain significance
rs56648089911:64,112,566C/G—uncertain significance
rs76905550411:64,112,573C/T—uncertain significance
rs76772002911:64,112,628C/T—uncertain significance
rs18679660811:64,116,825G/C—uncertain significance
rs75348496111:64,116,846G/A—uncertain significance
rs76578637811:64,116,863C/T—uncertain significance
rs14381046611:64,116,879C/T—uncertain significance
rs86869842311:64,116,918G/A—uncertain significance
rs20183398311:64,117,070C/T—uncertain significance
rs76927408311:64,117,121T/A—uncertain significance
rs77470772611:64,117,123G/A—uncertain significance
rs56612811:64,118,267G/Aintron variant—
rs37673532211:64,118,647G/A—uncertain significance
rs75028447511:64,118,672C/T—uncertain significance
rs146750700511:64,118,697G/C—uncertain significance
rs122261267811:64,118,956G/A—uncertain significance
rs148437746211:64,118,970A/G—uncertain significance
rs37294648511:64,119,030G/A—uncertain significance
rs36921232711:64,119,059C/T—uncertain significance
rs249591975811:64,119,650C/G—uncertain significance
rs249591980711:64,119,667G/T—uncertain significance
rs76665909511:64,119,728C/T—uncertain significance
rs37043311511:64,119,759G/A—uncertain significance
rs20101816511:64,120,220G/A—uncertain significance
rs76634180611:64,120,250G/A—uncertain significance
rs89946391511:64,120,307C/T—uncertain significance
rs76342502111:64,120,349G/A—uncertain significance
rs74604224511:64,120,593C/T—uncertain significance
rs77254047811:64,120,609G/A—uncertain significance
rs119808125611:64,120,693G/A—uncertain significance
rs57663011:64,120,706G/T—uncertain significance
rs6174662411:64,120,835C/T—benign
rs93441537011:64,120,839G/A—uncertain significance
rs77310078211:64,120,862C/T—uncertain significance
rs105684520111:64,120,863G/A—uncertain significance

Showing 100 of 122 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.