SCRIB

scribble planar cell polarity protein

Summary

This gene encodes a protein that was identified as being similar to the Drosophila scribble protein. The mammalian protein is involved in tumor suppression pathways. As a scaffold protein involved in cell polarization processes, this protein binds to many other proteins. The encoded protein binds to papillomavirus E6 protein via its PDZ domain and the C-terminus of E6. Two alternatively spliced transcript variants that encode different protein isoforms have been found for this gene. [provided by RefSeq, Nov 2011]

Known Variants201 total

rsidPosition (GRCh37)AllelesClassClinVar
rs15546324738:144,873,341G/A—uncertain significance
rs5400905728:144,873,361C/T—uncertain significance
rs3678503648:144,873,379C/A—uncertain significance
rs7825213168:144,873,422C/T—uncertain significance
rs7822919918:144,873,582G/A—uncertain significance
rs1498418488:144,873,606G/A—likely benign
rs7826761148:144,873,846T/C—uncertain significance
rs15546326928:144,873,874C/A—uncertain significance
rs25387685668:144,873,891A/C—uncertain significance
rs25387685778:144,873,895T/G—uncertain significance
rs5570945658:144,873,899T/C—likely benign
rs3701543818:144,874,056G/A—uncertain significance
rs1173387148:144,874,078T/C—benign
rs14562636298:144,874,170G/C—uncertain significance
rs11821638068:144,874,178G/A—uncertain significance
rs7825390788:144,874,190G/C—uncertain significance
rs7818012088:144,874,196G/T—uncertain significance
rs3743139608:144,874,230G/A—uncertain significance
rs7818166128:144,874,272C/T—uncertain significance
rs2021632698:144,874,307C/T—likely benign
rs3760378648:144,874,382G/A—likely benign
rs14795729428:144,874,439C/T—uncertain significance
rs3710827828:144,874,440G/A—likely benign
rs7819296528:144,874,453G/A—uncertain significance
rs10019277848:144,874,456C/T—uncertain significance
rs15546329838:144,874,461G/A—likely benign
rs3745903388:144,874,476C/T—likely benign
rs2019627218:144,874,533C/T—likely benign
rs7824515948:144,874,552G/A—uncertain significance
rs25387719358:144,874,685G/A—uncertain significance
rs7817933138:144,874,686G/A—uncertain significance
rs7824804808:144,874,695C/T—uncertain significance
rs7827466338:144,874,696C/G—uncertain significance
rs3738834138:144,874,706T/C—uncertain significance
rs5346644988:144,874,710C/T—likely benign
rs7818509948:144,874,770G/A—uncertain significance
rs1153603948:144,874,771C/T—benign
rs3721826438:144,874,812G/C—likely benign
rs1511866328:144,874,917C/A—uncertain significance
rs10260184478:144,874,944C/T—uncertain significance
rs726933518:144,874,957G/A—benign
rs18147630708:144,875,015G/C—uncertain significance
rs1123994318:144,875,026A/C—benign
rs12187199258:144,875,043G/A—likely benign
rs7824813348:144,875,045G/C—likely benign
rs1438088698:144,875,154G/A—benign
rs2021374648:144,875,168G/A—benign
rs15546333628:144,875,216T/C—uncertain significance
rs25387737168:144,875,240G/A—uncertain significance
rs117842178:144,875,242C/T—benign
rs18148244618:144,876,086G/T—uncertain significance
rs3709558038:144,876,093G/A—uncertain significance
rs13341391518:144,876,114C/T—uncertain significance
rs1493071548:144,877,226G/A—likely benign
rs3714511538:144,877,237C/T—uncertain significance
rs1463813718:144,877,245G/C—uncertain significance
rs2002465778:144,877,449C/A—uncertain significance
rs7823126468:144,877,461C/G—uncertain significance
rs7818389848:144,877,583C/T—likely benign
rs5578363288:144,880,318C/T——
rs3736734008:144,885,547G/A—likely benign
rs12313901838:144,885,563G/C—uncertain significance
rs15546354098:144,885,599A/G—uncertain significance
rs1422478688:144,885,601G/A—benign
rs9983102238:144,885,612C/T—uncertain significance
rs3776937958:144,885,621T/C—likely benign
rs1382577448:144,885,669G/C—benign
rs1409464408:144,885,701C/T—uncertain significance
rs7825273748:144,885,720C/T—uncertain significance
rs7823098518:144,885,730C/T—likely benign
rs13234296028:144,885,833C/A—uncertain significance
rs2017275118:144,885,849C/T—uncertain significance
rs25387955968:144,885,857T/G—uncertain significance
rs7819959978:144,885,935C/T—uncertain significance
rs7827456068:144,885,953G/A—uncertain significance
rs3751590148:144,885,962C/T—uncertain significance
rs11588088028:144,885,993G/A—uncertain significance
rs7818390778:144,886,089C/T—uncertain significance
rs7825600008:144,886,102C/T—likely benign
rs2010523798:144,886,206G/C—benign
rs1463637658:144,886,217T/G—uncertain significance
rs1409721278:144,886,269C/T—benign
rs5656420078:144,886,270G/A—likely benign
rs7824342848:144,886,272A/C—uncertain significance
rs2011563718:144,886,758C/G—uncertain significance
rs7822850858:144,886,792C/T—likely benign
rs7824245478:144,886,793G/C—uncertain significance
rs115423748:144,886,809T/C—benign
rs3732684088:144,886,849G/A—likely benign
rs18153318698:144,886,865T/C—uncertain significance
rs7827146558:144,886,887G/A—uncertain significance
rs1507302298:144,886,896C/A—uncertain significance
rs1499128108:144,886,920C/T—uncertain significance
rs7818597878:144,886,938C/T—uncertain significance
rs11653709248:144,886,955G/A—uncertain significance
rs3729174578:144,886,995T/C—uncertain significance
rs7819090658:144,887,175C/T—likely benign
rs7825154198:144,887,283G/A—uncertain significance
rs2001826408:144,887,285A/G—likely benign
rs7821664698:144,887,313T/C—uncertain significance

Showing 100 of 201 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.