CDC42BPB

CDC42 binding protein kinase beta

Summary

This gene encodes a member of the serine/threonine protein kinase family. The encoded protein contains a Cdc42/Rac-binding p21 binding domain resembling that of PAK kinase. The kinase domain of this protein is most closely related to that of myotonic dystrophy kinase-related ROK. Studies of the similar gene in rat suggested that this kinase may act as a downstream effector of Cdc42 in cytoskeletal reorganization. [provided by RefSeq, Jul 2008]

Known Variants200 total

rsidPosition (GRCh37)AllelesClassClinVar
rs76551091214:103,400,065G/A—uncertain significance
rs3523967514:103,400,082G/A—likely benign
rs14064050214:103,400,084G/C—uncertain significance
rs56255130914:103,400,098C/T—conflicting classifications of pathogenicity
rs77522633514:103,400,101T/C—uncertain significance
rs76030341014:103,400,102G/C—uncertain significance
rs213932534114:103,400,131G/A—uncertain significance
rs136447954814:103,400,132G/T—uncertain significance
rs36964722214:103,400,145C/T—likely benign
rs254271428214:103,400,155G/A—uncertain significance
rs1288476214:103,401,924T/Cdownstream gene variant—
rs13842631714:103,404,473T/A—likely benign
rs102674603914:103,404,474A/C—uncertain significance
rs56683618214:103,404,488C/T—uncertain significance
rs146790145414:103,404,508C/G—uncertain significance
rs5589789014:103,404,639G/T—benign
rs77332885814:103,404,681G/A—uncertain significance
rs77125653214:103,404,690C/A—uncertain significance
rs14879700414:103,404,709C/A—likely benign
rs13932314614:103,406,051C/G—likely benign
rs15000346414:103,406,055A/C—likely benign
rs6047522214:103,406,169C/T—benign
rs189180912814:103,406,192C/G—uncertain significance
rs254273651414:103,406,194G/A—uncertain significance
rs78093216314:103,406,207C/T—likely benign
rs254273657914:103,406,215C/T—uncertain significance
rs75392202714:103,406,256G/A—likely benign
rs20201608514:103,406,281G/A—likely benign
rs36955642514:103,406,301C/T—likely benign
rs254273750114:103,406,374A/C—likely benign
rs189182281614:103,406,425A/G—uncertain significance
rs254273857914:103,406,595A/G—uncertain significance
rs126044113214:103,406,599T/C—uncertain significance
rs148790039514:103,406,601C/T—uncertain significance
rs140877102914:103,410,230C/T—uncertain significance
rs76330684714:103,410,242G/A—uncertain significance
rs57752174514:103,410,278C/T—uncertain significance
rs254275592714:103,410,283T/C—uncertain significance
rs189202264214:103,410,294C/T—uncertain significance
rs94479907614:103,410,306T/C—uncertain significance
rs75169212714:103,410,401T/C—uncertain significance
rs14573722714:103,410,405G/A—benign
rs37197264314:103,410,468A/G—uncertain significance
rs77635513714:103,410,487C/T—likely benign
rs254275730614:103,410,506T/C—likely benign
rs117068471414:103,410,563T/C—uncertain significance
rs159545012514:103,410,587C/G—likely pathogenic
rs3582835214:103,410,595G/A—benign
rs53943967014:103,410,638G/A—likely benign
rs213936371014:103,410,651G/A—pathogenic
rs156684379114:103,410,687T/A—uncertain significance
rs14191230914:103,410,715C/T—likely benign
rs128434480114:103,410,718A/G—likely benign
rs136425142914:103,410,726G/A—uncertain significance
rs159545039314:103,410,740C/T—likely pathogenic
rs76517529914:103,410,753G/T—likely benign
rs126060317914:103,410,762T/C—likely benign
rs142352294414:103,412,014C/G—uncertain significance
rs20202644414:103,412,026G/A—likely benign
rs120379011014:103,412,041C/T—uncertain significance
rs213936990814:103,412,063T/G—uncertain significance
rs18819490014:103,412,797G/C—likely benign
rs77413923914:103,412,808C/T—uncertain significance
rs74739882014:103,412,853C/T—uncertain significance
rs77194594314:103,412,895G/A—uncertain significance
rs134668893114:103,412,938C/T—likely pathogenic
rs254277198814:103,412,960T/G—uncertain significance
rs78146418414:103,412,985T/C—likely benign
rs189219197714:103,413,002C/T—uncertain significance
rs254277829414:103,414,116G/A—uncertain significance
rs254277844514:103,414,138C/T—uncertain significance
rs1259096114:103,416,096A/G—benign
rs189239797414:103,416,120C/T—uncertain significance
rs103961160014:103,416,184C/G—uncertain significance
rs75972168714:103,416,228G/A—uncertain significance
rs77570371314:103,416,246G/A—uncertain significance
rs254279434714:103,416,808C/T—uncertain significance
rs94614568414:103,416,837C/T—uncertain significance
rs3489841014:103,416,839C/T—benign
rs3482237714:103,416,883T/C—benign
rs96385308814:103,416,939A/G—uncertain significance
rs254280475414:103,418,918A/C—uncertain significance
rs213940048514:103,418,942T/C—likely pathogenic
rs145624048514:103,420,962C/T—uncertain significance
rs14907799914:103,420,978C/T—likely benign
rs14216757014:103,420,979G/A—likely benign
rs254283166314:103,426,027G/A—uncertain significance
rs124620935514:103,426,045G/A—uncertain significance
rs3430139614:103,429,420T/C—benign
rs254284776314:103,430,838C/T—likely pathogenic
rs254284779714:103,430,849T/G—likely pathogenic
rs20009052214:103,430,854T/C—likely benign
rs77401081414:103,430,869T/C—uncertain significance
rs159547273914:103,430,938C/G—likely pathogenic
rs159547274114:103,430,939G/A—likely pathogenic
rs4551249514:103,430,940C/T—likely benign
rs159547275614:103,430,953A/G—likely pathogenic
rs159547276414:103,430,966G/A—pathogenic
rs131956876214:103,430,983G/A—uncertain significance
rs254285347214:103,432,620A/T—likely benign

Showing 100 of 200 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.