CNNM1

cyclin and CBS domain divalent metal cation transport mediator 1

Summary

This gene encodes a member of the ancient conserved domain protein family. The encoded protein may bind copper. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]

Known Variants62 total

rsidPosition (GRCh37)AllelesClassClinVar
rs5682964610:101,088,786C/A—benign
rs5675436410:101,088,930C/G—benign
rs98177488810:101,089,151G/A—uncertain significance
rs52768573210:101,089,247C/T—uncertain significance
rs74639693410:101,089,421A/C—uncertain significance
rs75725382310:101,089,428G/A—uncertain significance
rs101128613410:101,089,452C/A—uncertain significance
rs249396596910:101,089,453T/C—likely benign
rs128260391010:101,089,496G/A—uncertain significance
rs75661676610:101,089,503C/A—uncertain significance
rs135889767610:101,089,638G/C—uncertain significance
rs74963469910:101,089,670G/C—uncertain significance
rs77831236810:101,089,773G/T—uncertain significance
rs18390642510:101,089,783C/Tsynonymous variant—
rs7441979410:101,089,810G/A—benign
rs93173763710:101,089,955C/A—uncertain significance
rs77687145910:101,089,978G/C—uncertain significance
rs86902522610:101,090,101G/C—uncertain significance
rs249396996910:101,090,105A/G—uncertain significance
rs145193298010:101,090,114C/T—uncertain significance
rs76421214210:101,090,163A/G—uncertain significance
rs14494441310:101,090,246G/A—likely benign
rs14415744410:101,090,322C/T—uncertain significance
rs286260010:101,090,428G/T—benign
rs77329441210:101,090,693A/G—uncertain significance
rs249403362110:101,117,308A/C—uncertain significance
rs375089510:101,117,557A/G—benign
rs37086050910:101,120,624C/T—uncertain significance
rs147111342810:101,120,670C/T—uncertain significance
rs158990380110:101,120,682T/G—uncertain significance
rs376379210:101,120,787T/C—benign
rs203145931710:101,121,996T/C—uncertain significance
rs77205382410:101,122,052G/A—uncertain significance
rs14483357410:101,122,064C/G—uncertain significance
rs36931573410:101,122,115C/T—uncertain significance
rs249405217010:101,124,175G/A—uncertain significance
rs77082683810:101,124,189G/A—uncertain significance
rs75177573710:101,124,226C/T—uncertain significance
rs4153545210:101,124,600C/A—benign
rs203156425810:101,124,735A/G—uncertain significance
rs78059501610:101,136,818G/A—uncertain significance
rs15053839010:101,136,847C/T—uncertain significance
rs20110257010:101,136,887G/A—uncertain significance
rs125795428910:101,136,928A/C—uncertain significance
rs382921110:101,137,063A/G—benign
rs658427310:101,139,181G/Aintron variant—
rs249410470810:101,147,640C/T—uncertain significance
rs37639592410:101,147,647T/C—uncertain significance
rs229831610:101,147,692A/G—benign
rs77665110510:101,147,695G/A—uncertain significance
rs1749068210:101,147,720T/C—benign
rs37078114710:101,147,731C/T—uncertain significance
rs14311163410:101,147,915G/A—uncertain significance
rs76806644310:101,147,935C/T—uncertain significance
rs249410615610:101,147,936C/T—uncertain significance
rs14504460510:101,148,001G/A—uncertain significance
rs77378851010:101,148,034C/T—uncertain significance
rs11649566610:101,150,122G/A—uncertain significance
rs379393110:101,150,256G/A—benign
rs379393210:101,150,347A/C—benign
rs14961850110:101,151,248C/G—uncertain significance
rs442312310:101,152,720G/C——

Gene information from NCBI Gene. Variant classifications from ClinVar.