IL10RB

interleukin 10 receptor subunit beta

Summary

The protein encoded by this gene belongs to the cytokine receptor family. It is an accessory chain essential for the active interleukin 10 receptor complex. Coexpression of this and IL10RA proteins has been shown to be required for IL10-induced signal transduction. This gene and three other interferon receptor genes, IFAR2, IFNAR1, and IFNGR2, form a class II cytokine receptor gene cluster located in a small region on chromosome 21. [provided by RefSeq, Jul 2008]

Known Variants225 total

rsidPosition (GRCh37)AllelesClassClinVar
rs55633858321:34,638,677C/A—uncertain significance
rs5636858721:34,638,697C/A—uncertain significance
rs4560774321:34,638,699C/A—likely benign
rs102583586821:34,638,705A/T—uncertain significance
rs126663818921:34,638,771A/C—uncertain significance
rs116566759521:34,638,775C/T—uncertain significance
rs104235615521:34,638,790G/A—uncertain significance
rs92384604221:34,638,791C/T—likely benign
rs198894489921:34,638,794G/T—uncertain significance
rs37321842021:34,638,795C/T—likely benign
rs141397925321:34,638,797G/C—likely benign
rs251677626721:34,638,799G/C—uncertain significance
rs198894549421:34,638,805G/A—uncertain significance
rs93669291021:34,638,809G/A—likely benign
rs141678984821:34,638,810C/T—likely benign
rs212355658321:34,638,821T/G—likely pathogenic
rs105375067021:34,638,824G/A—uncertain significance
rs88987524721:34,638,827G/T—likely benign
rs121069334921:34,638,831G/A—likely benign
rs55987435321:34,638,838G/T—likely benign
rs223957321:34,638,859G/A—benign
rs19323594321:34,639,365G/Cregulatory region variant—
rs78167143021:34,640,679T/C—likely benign
rs125972587521:34,640,684G/A—likely benign
rs37754101321:34,640,695A/G—likely benign
rs251678046321:34,640,700A/G—likely benign
rs130680870921:34,640,701T/C—likely benign
rs74939392221:34,640,709G/A—uncertain significance
rs75965761021:34,640,721C/T—likely benign
rs8002757221:34,640,722G/A—likely benign
rs198901378221:34,640,728G/C—uncertain significance
rs97506541621:34,640,734A/G—uncertain significance
rs198901399721:34,640,740T/A—uncertain significance
rs212356111321:34,640,756A/C—uncertain significance
rs251678069121:34,640,765A/G—uncertain significance
rs198901446821:34,640,769G/A—pathogenic
rs75365011021:34,640,771A/G—uncertain significance
rs14049501421:34,640,772G/A—likely benign
rs57415888721:34,640,779G/A—uncertain significance
rs18207343121:34,640,780C/T—likely benign
rs198901487621:34,640,781T/A—likely benign
rs20120537221:34,640,787C/T—likely benign
rs283416721:34,640,788A/Gmissense variantrisk factor
rs88696563721:34,640,793G/C—likely benign
rs78172945221:34,640,796C/T—likely benign
rs75648359121:34,640,799G/A—likely benign
rs198901573221:34,640,806A/C—uncertain significance
rs212356127221:34,640,824T/G—pathogenic
rs14821589421:34,640,841T/C—benign
rs228455221:34,644,082G/Tintron variant—
rs77910563321:34,648,883A/G—likely benign
rs20047268421:34,648,887T/G—conflicting classifications of pathogenicity
rs198917584821:34,648,900G/A—likely pathogenic
rs209647850521:34,648,904T/C—likely benign
rs120469086921:34,648,906G/C—uncertain significance
rs126935242021:34,648,921A/G—uncertain significance
rs90287775521:34,648,930A/T—uncertain significance
rs96866214221:34,648,934T/C—likely benign
rs14846678221:34,648,942C/T—conflicting classifications of pathogenicity
rs20166497421:34,648,986T/C—likely benign
rs212357387921:34,649,001G/C—uncertain significance
rs75923549021:34,649,011A/T—uncertain significance
rs86860419721:34,649,025T/G—uncertain significance
rs251679066821:34,649,027G/A—pathogenic
rs74540352621:34,649,028G/C—uncertain significance
rs212357391721:34,649,029T/C—uncertain significance
rs198917874321:34,649,038C/T—uncertain significance
rs212357394021:34,649,039C/T—likely benign
rs75758172821:34,649,055G/A—uncertain significance
rs198917920521:34,649,059G/C—likely pathogenic
rs198917923221:34,649,062A/T—uncertain significance
rs228502021:34,649,123G/A—benign
rs53176563521:34,652,046C/T—conflicting classifications of pathogenicity
rs76959531021:34,652,057C/G—uncertain significance
rs92687354521:34,652,068C/A—uncertain significance
rs198924611121:34,652,085A/G—likely benign
rs198924617321:34,652,092C/T—uncertain significance
rs251679458721:34,652,097T/G—likely benign
rs116360043321:34,652,102C/T—uncertain significance
rs77399627121:34,652,108A/T—uncertain significance
rs75424645221:34,652,110A/G—uncertain significance
rs75932151721:34,652,111T/G—uncertain significance
rs13813490421:34,652,113C/T—likely benign
rs77514037021:34,652,114G/A—uncertain significance
rs76558823521:34,652,145C/T—likely benign
rs38790732621:34,652,146G/Tstop gainedpathogenic
rs53938972921:34,652,157T/A—likely benign
rs14955413021:34,652,160G/A—uncertain significance
rs4554513821:34,652,167G/A—conflicting classifications of pathogenicity
rs148448899721:34,652,169G/C—likely benign
rs118671902621:34,652,171A/G—uncertain significance
rs14152358221:34,652,175C/T—likely benign
rs13888323721:34,652,190T/C—benign
rs117025467221:34,652,191G/A—uncertain significance
rs137335453321:34,652,201G/A—pathogenic
rs12190960121:34,652,202G/Astop gainedpathogenic
rs6173577621:34,652,208C/T—benign
rs77098069321:34,652,209G/A—uncertain significance
rs198924979021:34,652,223G/C—uncertain significance
rs122970550121:34,652,242A/G—likely benign

Showing 100 of 225 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.