RANBP3

RAN binding protein 3

Summary

This gene encodes a protein with a RanBD1 domain that is found in both the nucleus and cytoplasm. This protein plays a role in nuclear export as part of a heteromeric complex. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

Known Variants33 total

rsidPosition (GRCh37)AllelesClassClinVar
rs77857392019:5,917,632C/T—uncertain significance
rs37734569119:5,917,653C/T—uncertain significance
rs18804500619:5,918,584C/T—uncertain significance
rs95354630819:5,918,637T/C—uncertain significance
rs138236756819:5,921,217C/T—uncertain significance
rs251291754619:5,921,238T/C—uncertain significance
rs75352559919:5,923,270G/A—uncertain significance
rs1041788519:5,924,893G/A—benign
rs94741542019:5,924,896C/T—uncertain significance
rs137446362919:5,925,679C/T—uncertain significance
rs57455075219:5,925,694C/T—uncertain significance
rs20038387419:5,925,703G/A—uncertain significance
rs19969748919:5,925,733C/T—uncertain significance
rs102849629419:5,932,468T/G—uncertain significance
rs20217726419:5,932,523G/A—uncertain significance
rs74670510019:5,933,428C/T—uncertain significance
rs77148720819:5,933,469C/T—uncertain significance
rs13931138119:5,936,552C/Tintron variant—
rs76160571819:5,941,834C/T—uncertain significance
rs725299319:5,945,568C/T——
rs37764838719:5,951,409C/T—uncertain significance
rs117509337419:5,951,420G/A—uncertain significance
rs75489683919:5,951,459G/A—uncertain significance
rs76954629619:5,951,469C/G—uncertain significance
rs77738723019:5,951,528C/T—uncertain significance
rs77041945419:5,951,531G/A—uncertain significance
rs128505790719:5,951,534C/T—uncertain significance
rs54345929219:5,951,559C/T—uncertain significance
rs75074284019:5,951,562G/A—uncertain significance
rs56311083519:5,951,576G/A—uncertain significance
rs37414933919:5,951,586A/T—uncertain significance
rs77044902019:5,957,955C/G—uncertain significance
rs74708852119:5,978,084G/C—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.