MS4A1

membrane spanning 4-domains A1

Summary

This gene encodes a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. This gene encodes a B-lymphocyte surface molecule which plays a role in the development and differentiation of B-cells into plasma cells. This family member is localized to 11q12, among a cluster of family members. Alternative splicing of this gene results in two transcript variants which encode the same protein. [provided by RefSeq, Jul 2008]

Known Variants141 total

rsidPosition (GRCh37)AllelesClassClinVar
rs53312006411:60,225,304T/C——
rs1715501911:60,229,677C/T—benign
rs213519710911:60,229,856A/G—likely benign
rs20076809911:60,229,857C/T—uncertain significance
rs76358837311:60,229,882T/A—uncertain significance
rs14380788911:60,229,885C/T—uncertain significance
rs3410976811:60,229,886G/A—likely benign
rs76622766011:60,229,887G/A—uncertain significance
rs140906661311:60,229,889A/G—likely benign
rs213519718411:60,229,892G/T—likely benign
rs76889270511:60,229,894C/T—uncertain significance
rs75461036811:60,229,895A/G—likely benign
rs20149190011:60,229,897T/C—uncertain significance
rs75231101611:60,229,898G/A—uncertain significance
rs249539862211:60,229,902G/T—uncertain significance
rs213519722211:60,229,906C/T—uncertain significance
rs127376891711:60,229,907T/C—likely benign
rs213519724311:60,229,912C/A—uncertain significance
rs134332826811:60,229,913T/C—likely benign
rs120498309111:60,229,914A/G—uncertain significance
rs20135493811:60,229,917C/T—uncertain significance
rs249539872611:60,229,921C/A—uncertain significance
rs145388957211:60,229,924G/T—uncertain significance
rs213519730111:60,229,933C/T—uncertain significance
rs74723987611:60,229,945G/A—uncertain significance
rs249539901311:60,229,957T/G—uncertain significance
rs20080505911:60,229,958G/C—benign
rs132224814111:60,229,962G/A—uncertain significance
rs77322275911:60,229,966C/A—uncertain significance
rs213519740611:60,229,968A/T—uncertain significance
rs14775487411:60,229,969C/T—uncertain significance
rs15006175611:60,229,970G/A—benign
rs208625687111:60,230,004G/C—uncertain significance
rs20058733611:60,230,016T/C—likely benign
rs118639578011:60,230,025A/G—likely benign
rs18592049411:60,230,457C/G—likely benign
rs249540141111:60,230,468T/A—likely benign
rs20072417411:60,230,471C/T—likely benign
rs147355572611:60,230,495G/A—likely benign
rs77523455711:60,230,498C/T—likely benign
rs213519809811:60,230,505A/G—uncertain significance
rs14662692611:60,230,509C/T—uncertain significance
rs139694838911:60,230,513G/T—likely benign
rs128900330411:60,230,521T/C—uncertain significance
rs7970327411:60,230,523C/T—benign
rs123705700511:60,230,530T/A—uncertain significance
rs207077011:60,230,531C/T—benign
rs55835826511:60,230,541A/T—uncertain significance
rs19974724011:60,230,550C/A—uncertain significance
rs11643386311:60,230,577C/A—likely benign
rs116760211511:60,230,588C/A—likely benign
rs213519831111:60,230,595G/A—uncertain significance
rs1079227811:60,230,722T/G—benign
rs712635411:60,231,066C/A——
rs208627224311:60,231,741C/T—likely benign
rs20196205911:60,231,772C/T—likely benign
rs37147994711:60,231,773G/A—uncertain significance
rs20166570611:60,231,792C/T—uncertain significance
rs20026591211:60,231,793G/A—likely benign
rs26760305511:60,231,796G/C—uncertain significance
rs20136136311:60,231,809A/G—uncertain significance
rs76835920311:60,231,825A/T—likely benign
rs37247640111:60,231,827C/T—likely benign
rs20221635611:60,231,829T/C—likely benign
rs77588142811:60,231,834C/A—likely benign
rs37701294511:60,231,835C/T—likely benign
rs414687011:60,231,986A/G—benign
rs493936411:60,232,325A/T——
rs213520149511:60,233,394G/A—uncertain significance
rs77725926011:60,233,401G/A—uncertain significance
rs20124538711:60,233,409A/C—uncertain significance
rs19986098411:60,233,410T/C—uncertain significance
rs167235103211:60,233,450G/T—uncertain significance
rs249541032611:60,233,454C/A—uncertain significance
rs249541033711:60,233,462C/T—likely benign
rs208628821111:60,233,505G/C—uncertain significance
rs20149511811:60,233,512T/C—uncertain significance
rs249541064611:60,233,532A/G—uncertain significance
rs75700427011:60,233,533C/T—uncertain significance
rs74543749311:60,233,538T/G—uncertain significance
rs249541072411:60,233,551A/T—uncertain significance
rs119081931311:60,233,579G/A—likely benign
rs20178418611:60,233,589C/T—uncertain significance
rs213520187411:60,233,590C/T—uncertain significance
rs54760495111:60,233,594T/C—likely benign
rs77867025111:60,233,596C/A—uncertain significance
rs135945226811:60,233,602A/G—uncertain significance
rs249541103611:60,233,603C/T—likely benign
rs129267341711:60,233,610A/T—uncertain significance
rs37584758111:60,233,613A/C—uncertain significance
rs77965518511:60,233,614T/C—uncertain significance
rs135027966211:60,233,631G/T—uncertain significance
rs20182631411:60,233,634A/G—uncertain significance
rs249541128111:60,233,648G/A—uncertain significance
rs249541128711:60,233,649T/A—likely benign
rs213520304011:60,234,448T/C—uncertain significance
rs18417455211:60,234,455C/G—uncertain significance
rs249541390611:60,234,466T/G—uncertain significance
rs249541398911:60,234,478T/G—uncertain significance
rs249541401711:60,234,482A/G—uncertain significance

Showing 100 of 141 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.