CD79A

CD79a molecule

Summary

The B lymphocyte antigen receptor is a multimeric complex that includes the antigen-specific component, surface immunoglobulin (Ig). Surface Ig non-covalently associates with two other proteins, Ig-alpha and Ig-beta, which are necessary for expression and function of the B-cell antigen receptor. This gene encodes the Ig-alpha protein of the B-cell antigen component. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

Known Variants145 total

rsidPosition (GRCh37)AllelesClassClinVar
rs142892219:42,379,780G/Aregulatory region variant—
rs53010249619:42,380,226C/T——
rs78220637319:42,381,382G/C—uncertain significance
rs78219596719:42,381,386T/G—likely benign
rs14648036619:42,381,387C/T—uncertain significance
rs78274661519:42,381,395C/T—likely benign
rs212330146719:42,381,398C/T—likely benign
rs37118468919:42,381,402G/A—conflicting classifications of pathogenicity
rs78271615919:42,381,404T/C—likely benign
rs251369599919:42,381,425C/A—likely benign
rs14103366919:42,381,428C/A—likely benign
rs104494414319:42,381,435C/T—likely benign
rs160062999819:42,381,438T/A—uncertain significance
rs37760848319:42,381,459T/C—uncertain significance
rs78217611219:42,381,461G/A—likely benign
rs78266530319:42,381,467G/A—likely benign
rs7698368119:42,382,757G/A—benign
rs155584343919:42,383,048G/A—likely benign
rs78187452819:42,383,057C/T—uncertain significance
rs207420442719:42,383,060G/T—uncertain significance
rs251369867119:42,383,061C/G—likely benign
rs212330373719:42,383,067G/C—likely benign
rs251369874619:42,383,088C/T—likely benign
rs251369878319:42,383,100A/C—likely benign
rs78242159019:42,383,108T/A—uncertain significance
rs19960306219:42,383,114G/C—uncertain significance
rs207420485919:42,383,117T/C—uncertain significance
rs78230250319:42,383,127C/T—likely benign
rs160063108119:42,383,130C/T—likely benign
rs76475829219:42,383,144C/T—conflicting classifications of pathogenicity
rs14484738219:42,383,145G/A—likely benign
rs37031364219:42,383,159A/G—uncertain significance
rs207420531719:42,383,162A/T—uncertain significance
rs78179230519:42,383,163C/T—likely benign
rs78246737619:42,383,164G/A—uncertain significance
rs15122466119:42,383,168A/G—uncertain significance
rs14004768819:42,383,169C/T—likely benign
rs37404194119:42,383,170G/A—uncertain significance
rs156880171619:42,383,178G/A—pathogenic
rs78265764119:42,383,182C/T—uncertain significance
rs78250715019:42,383,183G/A—conflicting classifications of pathogenicity
rs15029711019:42,383,184C/T—likely benign
rs207420561519:42,383,190C/A—likely benign
rs19996739319:42,383,204C/A—uncertain significance
rs148716671119:42,383,205G/A—likely benign
rs207420588719:42,383,222T/C—uncertain significance
rs78194943219:42,383,233G/A—uncertain significance
rs58777816619:42,383,238C/A—uncertain significance
rs138383001419:42,383,239C/T—uncertain significance
rs57067384519:42,383,243A/G—uncertain significance
rs13795307919:42,383,249C/T—uncertain significance
rs78187539319:42,383,250G/A—likely benign
rs11707841419:42,383,281G/A—likely benign
rs11301928619:42,383,289A/G—conflicting classifications of pathogenicity
rs212330424119:42,383,290T/C—uncertain significance
rs20066717419:42,383,292C/T—likely benign
rs78266187419:42,383,293G/A—uncertain significance
rs14351120319:42,383,300G/A—uncertain significance
rs160063129419:42,383,303T/G—pathogenic
rs78249291819:42,383,307G/A—likely benign
rs78220763919:42,383,315A/G—uncertain significance
rs160063131619:42,383,316C/T—likely benign
rs251369940619:42,383,318A/G—uncertain significance
rs14589540919:42,383,321C/T—uncertain significance
rs13845434419:42,383,337C/T—likely benign
rs78228265419:42,383,338G/A—uncertain significance
rs14400638019:42,383,350C/T—uncertain significance
rs14436748719:42,383,351G/A—uncertain significance
rs37761573219:42,383,352C/T—likely benign
rs54848711219:42,383,353G/A—uncertain significance
rs212330441019:42,383,354T/G—uncertain significance
rs160063135019:42,383,355G/A—likely benign
rs78270938119:42,383,357G/A—uncertain significance
rs155584360119:42,383,360G/A—likely pathogenic
rs251369952519:42,383,362G/A—uncertain significance
rs56330786719:42,383,378G/T—likely benign
rs133415894819:42,383,591C/A—likely benign
rs155584368419:42,383,597C/T—likely benign
rs160063159319:42,383,603A/G—pathogenic
rs78201453419:42,383,609G/A—likely benign
rs117488821119:42,383,612C/T—likely benign
rs78275177619:42,383,619C/A—uncertain significance
rs20120628119:42,383,620C/T—uncertain significance
rs212330494919:42,383,625C/T—likely benign
rs146225791219:42,383,641G/A—uncertain significance
rs14879798719:42,383,644C/A—conflicting classifications of pathogenicity
rs251370030119:42,383,652C/A—likely benign
rs155584373219:42,383,653G/A—uncertain significance
rs207420942619:42,383,667G/A—uncertain significance
rs122182107319:42,383,677T/C—uncertain significance
rs134969271319:42,383,678C/T—likely benign
rs155584376019:42,383,684G/A—likely benign
rs53767591419:42,383,690C/T—likely benign
rs78215007319:42,383,691G/A—uncertain significance
rs20209718719:42,383,692C/T—uncertain significance
rs132085259719:42,383,694G/A—uncertain significance
rs78198411719:42,383,708G/A—likely benign
rs78224424819:42,383,718T/C—uncertain significance
rs212330522519:42,383,723G/C—uncertain significance
rs148783241519:42,383,729C/A—uncertain significance

Showing 100 of 145 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.