NRIP1

nuclear receptor interacting protein 1

Summary

Nuclear receptor interacting protein 1 (NRIP1) is a nuclear protein that specifically interacts with the hormone-dependent activation domain AF2 of nuclear receptors. Also known as RIP140, this protein modulates transcriptional activity of the estrogen receptor. [provided by RefSeq, Jul 2008]

Known Variants204 total

rsidPosition (GRCh37)AllelesClassClinVar
rs57339597721:16,335,004A/G——
rs105693021:16,336,804T/G——
rs76963877221:16,337,049T/A—uncertain significance
rs14881453121:16,337,059G/A—likely benign
rs55175249121:16,337,066C/T—uncertain significance
rs124300979621:16,337,071C/T—uncertain significance
rs6173344121:16,337,084A/C—likely benign
rs20130862221:16,337,088T/C—benign
rs75119397121:16,337,100G/A—benign
rs14030710021:16,337,102T/C—likely benign
rs14521600421:16,337,106T/G—likely benign
rs6175020721:16,337,111G/A—benign
rs251622867621:16,337,113G/A—uncertain significance
rs37767959921:16,337,129T/C—uncertain significance
rs57793877921:16,337,150T/C—uncertain significance
rs75122918721:16,337,165A/C—uncertain significance
rs20066270221:16,337,176T/G—uncertain significance
rs6173344221:16,337,184A/G—benign
rs18573242821:16,337,201T/C—benign
rs7450386221:16,337,211C/G—conflicting classifications of pathogenicity
rs77478706321:16,337,220A/T—uncertain significance
rs76984106921:16,337,227G/C—uncertain significance
rs156893453621:16,337,252C/T—uncertain significance
rs132959959321:16,337,270G/C—uncertain significance
rs14731065021:16,337,275G/A—uncertain significance
rs14080349521:16,337,279C/A—conflicting classifications of pathogenicity
rs20011115821:16,337,304G/A—likely benign
rs76118827021:16,337,356T/G—uncertain significance
rs75029828721:16,337,367C/T—likely benign
rs37374989621:16,337,391G/C—benign
rs208669072921:16,337,393G/T—uncertain significance
rs2870765421:16,337,448C/A—benign
rs2858716221:16,337,538G/A—benign
rs101260702321:16,337,549T/A—uncertain significance
rs251624063421:16,337,557T/C—uncertain significance
rs14363880921:16,337,602T/C—conflicting classifications of pathogenicity
rs86623559521:16,337,644A/C—uncertain significance
rs141002548721:16,337,658G/C—uncertain significance
rs222850821:16,337,661C/T—benign
rs54906742021:16,337,662G/A—uncertain significance
rs56902686221:16,337,674C/T—likely benign
rs14504296621:16,337,675G/T—likely benign
rs135338672421:16,337,680C/G—uncertain significance
rs251624455221:16,337,738A/G—uncertain significance
rs75544710921:16,337,756C/T—uncertain significance
rs36948420621:16,337,757G/A—likely benign
rs7736082221:16,337,764G/A—benign
rs251624529721:16,337,772A/C—likely benign
rs74530812021:16,337,808A/C—conflicting classifications of pathogenicity
rs57154108321:16,337,809A/C—likely benign
rs251624620421:16,337,816G/A—likely benign
rs77544774621:16,337,822C/T—uncertain significance
rs208670959021:16,337,856G/C—likely benign
rs75961247321:16,337,885T/C—likely benign
rs36988427021:16,337,960G/C—uncertain significance
rs14335916521:16,337,963T/A—uncertain significance
rs131738644021:16,338,028C/T—uncertain significance
rs251625162321:16,338,055C/T—uncertain significance
rs74609471721:16,338,060C/T—likely benign
rs77213208921:16,338,064C/A—uncertain significance
rs76452355821:16,338,068T/A—uncertain significance
rs37762883121:16,338,102C/A—uncertain significance
rs6175020821:16,338,106G/A—benign
rs14035231621:16,338,119C/T—uncertain significance
rs14593412121:16,338,120G/A—benign
rs6175505921:16,338,139G/A—uncertain significance
rs14800966121:16,338,140C/T—likely benign
rs77365846921:16,338,160G/A—uncertain significance
rs75118336621:16,338,171G/A—likely benign
rs36950630921:16,338,179C/A—uncertain significance
rs76891353621:16,338,224G/T—uncertain significance
rs56796259821:16,338,235C/T—uncertain significance
rs14065358721:16,338,236A/T—conflicting classifications of pathogenicity
rs99734895521:16,338,250A/C—uncertain significance
rs251625568821:16,338,257C/G—uncertain significance
rs13832391021:16,338,259A/G—likely benign
rs37636311521:16,338,262A/C—uncertain significance
rs76005206821:16,338,285C/T—likely benign
rs214692522821:16,338,287C/T—uncertain significance
rs6175097321:16,338,294T/C—benign
rs14729371321:16,338,313C/T—conflicting classifications of pathogenicity
rs208672570921:16,338,325T/C—uncertain significance
rs76973180821:16,338,328T/C—uncertain significance
rs19984173321:16,338,357G/C—uncertain significance
rs19118550921:16,338,368G/A—uncertain significance
rs75285944121:16,338,401T/G—uncertain significance
rs14323074021:16,338,408T/C—likely benign
rs37448060521:16,338,420A/G—likely benign
rs55868951121:16,338,428G/A—uncertain significance
rs251625985821:16,338,434G/C—uncertain significance
rs6175505821:16,338,443G/A—likely benign
rs54123865521:16,338,476C/T—likely benign
rs37188114921:16,338,493A/C—uncertain significance
rs57455278721:16,338,523C/T—uncertain significance
rs15062383421:16,338,581C/G—uncertain significance
rs74789497121:16,338,582T/G—likely benign
rs77334278921:16,338,620G/C—uncertain significance
rs98502295521:16,338,642C/T—likely benign
rs75839937921:16,338,643G/A—uncertain significance
rs214692873421:16,338,646G/A—uncertain significance

Showing 100 of 204 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.