BICC1

BicC family RNA binding protein 1

Summary

This gene encodes an RNA-binding protein that is active in regulating gene expression by modulating protein translation during embryonic development. Mouse studies identified the corresponding protein to be under strict control during cell differentiation and to be a maternally provided gene product. [provided by RefSeq, Apr 2009]

Known Variants272 total

rsidPosition (GRCh37)AllelesClassClinVar
rs707477810:60,272,248C/A——
rs11259753810:60,272,708T/C—benign
rs57266402010:60,272,808C/T—likely benign
rs18429132110:60,272,853G/A—benign
rs75824856910:60,272,924C/T—likely benign
rs249230427110:60,272,929A/T—uncertain significance
rs76856023310:60,272,931C/T—likely benign
rs78113463210:60,272,935C/G—uncertain significance
rs76928022010:60,272,944C/T—uncertain significance
rs135646923610:60,272,949C/A—uncertain significance
rs249230522410:60,273,024C/T—likely benign
rs136717836510:60,273,032C/G—uncertain significance
rs20024820710:60,273,034C/T—likely benign
rs76924410410:60,273,041G/T—uncertain significance
rs105121280610:60,273,074A/G—likely benign
rs53779901210:60,273,084A/G—uncertain significance
rs710047410:60,273,121T/C—benign
rs707964810:60,273,155C/A—benign
rs1076355110:60,273,898G/Aintron variant—
rs789729810:60,274,606T/Cintron variant—
rs142720010:60,274,928C/Tintron variant—
rs189624610:60,276,068A/Gregulatory region variant—
rs5739624810:60,281,530T/G——
rs2885517610:60,282,570G/C——
rs2880782210:60,282,604G/C——
rs14967535110:60,282,639T/A——
rs941670310:60,283,008A/T——
rs739258410:60,283,090C/Tintron variant—
rs739439510:60,283,187G/Aintron variant—
rs708963610:60,283,309T/C——
rs739255710:60,283,524G/A——
rs15050525810:60,284,763C/Aintron variant—
rs1159424010:60,284,785G/Cintron variant—
rs1159323010:60,284,875T/A——
rs1159274810:60,284,915A/T——
rs164901610:60,288,540T/G——
rs164908210:60,292,434A/G——
rs164908110:60,292,444G/Aintron variant—
rs164907810:60,293,320A/G——
rs165845710:60,302,716T/A——
rs6736235110:60,306,548C/Aintron variant—
rs99101610:60,311,724T/G——
rs165844810:60,312,244C/A——
rs1256955910:60,312,711T/A——
rs165844210:60,318,897G/Aintron variant—
rs165844110:60,323,021G/T——
rs165843610:60,326,910G/Aintron variant—
rs164904510:60,327,047T/Cintron variant—
rs165843510:60,327,527A/Gintron variant—
rs291794910:60,329,166G/Aintron variant—
rs257739110:60,329,186T/A——
rs165842510:60,331,547G/Cintron variant—
rs198217310:60,334,002G/C——
rs414167110:60,338,753T/A——
rs239344910:60,343,030A/T——
rs494852510:60,361,270G/Aintron variant—
rs424559910:60,365,755A/T——
rs3544483110:60,375,613G/Aintron variant—
rs7468799010:60,380,553T/C—benign
rs77708423710:60,380,597G/A—likely benign
rs76415429210:60,380,631A/G—likely benign
rs249289548110:60,380,661G/A—uncertain significance
rs36814407310:60,380,669G/A—likely benign
rs11560618910:60,380,705A/G—likely benign
rs38790712310:60,461,855C/T—risk factor
rs54198501710:60,461,884C/T—likely benign
rs494854010:60,462,096C/G—benign
rs148537590710:60,544,765C/G—likely benign
rs118285916310:60,544,822G/A—uncertain significance
rs77883278510:60,544,841G/C—likely pathogenic
rs184297293810:60,544,854A/G—likely benign
rs1235666410:60,545,045C/T—benign
rs1100626110:60,545,061C/A—benign
rs11778272810:60,545,086G/A—likely benign
rs7543613310:60,545,112C/T—likely benign
rs184302687910:60,546,704A/G—uncertain significance
rs14499168510:60,546,739C/T—likely benign
rs52748125410:60,546,782G/A—uncertain significance
rs213279694210:60,546,801C/G—uncertain significance
rs11598868110:60,547,912A/G—likely benign
rs156461373910:60,548,127T/C—uncertain significance
rs14114147110:60,548,132A/G—likely benign
rs37591784710:60,548,136A/G—benign
rs249376463610:60,548,184G/A—uncertain significance
rs53239999910:60,548,190A/G—likely benign
rs54709661110:60,548,198C/G—likely benign
rs1181256710:60,548,276G/A—benign
rs708759210:60,548,833G/A—benign
rs707704110:60,548,963C/T—likely benign
rs184310269810:60,549,004C/G—likely benign
rs11156930510:60,549,015A/G—likely benign
rs14296294610:60,549,037G/A—benign
rs55045523510:60,549,058A/G—benign
rs75812595910:60,549,077C/T—uncertain significance
rs14746645110:60,549,127A/C—conflicting classifications of pathogenicity
rs53208654910:60,549,128A/G—uncertain significance
rs249377106310:60,549,157C/T—uncertain significance
rs122572504310:60,549,159A/C—likely benign
rs76619355610:60,549,196A/G—uncertain significance
rs20167965410:60,549,211G/T—uncertain significance

Showing 100 of 272 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.