CAPRIN2

caprin family member 2

Summary

The protein encoded by this gene may regulate the transport of mRNA. It may play a role in the differentiation of erythroblasts. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]

Known Variants60 total

rsidPosition (GRCh37)AllelesClassClinVar
rs76639870712:30,862,867G/A—uncertain significance
rs14254787012:30,863,249G/A—uncertain significance
rs15095180912:30,863,255C/T—uncertain significance
rs76367611012:30,863,357C/T—uncertain significance
rs15008553612:30,864,505G/A—uncertain significance
rs75260765712:30,864,514C/T—uncertain significance
rs138966056312:30,864,520C/T—uncertain significance
rs20034601012:30,864,530T/A—uncertain significance
rs20158722012:30,866,733G/A—uncertain significance
rs156554245612:30,866,744T/C—uncertain significance
rs321389512:30,866,806A/G—benign
rs37112824312:30,867,968G/A—uncertain significance
rs7830300812:30,868,008C/T—benign
rs37528406712:30,868,030A/G—uncertain significance
rs74938411512:30,869,494C/A—uncertain significance
rs205764814612:30,869,522G/A—uncertain significance
rs36812170712:30,869,528C/T—uncertain significance
rs77417201912:30,869,555G/A—uncertain significance
rs14811014012:30,869,571G/T—uncertain significance
rs54597846212:30,872,016C/A—uncertain significance
rs135969097412:30,872,027G/C—uncertain significance
rs3408742112:30,872,061A/G—benign
rs13997571012:30,872,105T/C—uncertain significance
rs76305550112:30,872,129A/C—uncertain significance
rs7307996212:30,872,178G/Aregulatory region variant—
rs7307997012:30,873,116C/Tintron variant—
rs56093020212:30,873,773G/A—uncertain significance
rs11173887812:30,876,188G/A—benign
rs144458796512:30,877,315C/G—uncertain significance
rs230462812:30,877,327G/A—uncertain significance
rs20073860812:30,877,333G/A—uncertain significance
rs54729360612:30,878,922T/C—uncertain significance
rs250101120112:30,878,994C/G—uncertain significance
rs11477673112:30,879,032A/G—benign
rs119506669312:30,881,611G/A—uncertain significance
rs77846604312:30,881,649A/G—uncertain significance
rs77181167812:30,881,653C/T—uncertain significance
rs206170775212:30,881,769G/C—uncertain significance
rs250192458012:30,882,133C/G—uncertain significance
rs148512934912:30,882,163G/A—uncertain significance
rs206261832512:30,884,283C/G—uncertain significance
rs206263571512:30,884,323T/G—likely benign
rs6173541412:30,884,336A/G—benign
rs206264433312:30,884,363T/C—uncertain significance
rs57478613512:30,884,366T/C—likely benign
rs250240197412:30,884,430C/T—uncertain significance
rs250240412412:30,884,438T/A—uncertain significance
rs37557806112:30,888,006G/C—uncertain significance
rs76136199912:30,888,056G/T—uncertain significance
rs37193412212:30,888,130G/A—uncertain significance
rs37658348212:30,893,967C/T—uncertain significance
rs74822252212:30,894,034C/T—uncertain significance
rs37000361812:30,906,325C/G—uncertain significance
rs14506905212:30,906,372C/T—uncertain significance
rs77643546112:30,906,404C/G—uncertain significance
rs101372187212:30,906,419C/A—uncertain significance
rs250586921612:30,906,484C/T—uncertain significance
rs18484218512:30,906,529T/C—uncertain significance
rs76071785512:30,906,583T/G—uncertain significance
rs13808983712:30,906,629C/A—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.