TRAPPC9

trafficking protein particle complex subunit 9

Summary

This gene encodes a protein that likely plays a role in NF-kappa-B signaling. Mutations in this gene have been associated with autosomal-recessive cognitive disability. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010]

Known Variants764 total

rsidPosition (GRCh37)AllelesClassClinVar
rs1383121448:140,742,627A/G—uncertain significance
rs7589247268:140,742,728C/T—uncertain significance
rs1875941978:140,742,772C/T—conflicting classifications of pathogenicity
rs794080268:140,742,929G/A—likely benign
rs5487290548:140,742,973G/A—uncertain significance
rs1903033498:140,743,019T/G—uncertain significance
rs5653621448:140,743,123C/T—uncertain significance
rs1174430488:140,743,139C/G—likely benign
rs1992268:140,743,200G/A—benign
rs8860627218:140,743,224C/G—uncertain significance
rs3732841528:140,743,239G/C—uncertain significance
rs5749083248:140,743,313C/T—likely benign
rs7540619068:140,743,314G/A—uncertain significance
rs18177873158:140,743,315C/G—uncertain significance
rs1401572078:140,743,330C/T—conflicting classifications of pathogenicity
rs1456692048:140,743,331G/A—likely benign
rs1471272798:140,743,337A/C—conflicting classifications of pathogenicity
rs3739793058:140,743,340G/T—conflicting classifications of pathogenicity
rs13242905258:140,743,346G/T—uncertain significance
rs21299217888:140,743,351A/T—uncertain significance
rs1433961248:140,743,361T/G—likely benign
rs12667849598:140,743,365A/G—uncertain significance
rs7679632168:140,743,387C/T—uncertain significance
rs1496767098:140,743,388G/A—likely benign
rs1455035518:140,743,395C/T—conflicting classifications of pathogenicity
rs21299224728:140,743,400G/A—likely benign
rs24885039608:140,743,404A/G—uncertain significance
rs3714030798:140,743,426G/T—uncertain significance
rs7796018748:140,743,427G/A—likely benign
rs3720392918:140,743,433G/A—likely benign
rs7740144788:140,743,441C/T—uncertain significance
rs7615038048:140,743,451C/T—likely benign
rs5367879648:140,743,459C/G—uncertain significance
rs1488575758:140,743,460G/A—conflicting classifications of pathogenicity
rs5706882488:140,743,463C/T—conflicting classifications of pathogenicity
rs7529409048:140,743,479G/C—conflicting classifications of pathogenicity
rs1165112608:140,743,605C/T—likely benign
rs589333858:140,743,617G/T—benign
rs1128856318:140,743,763G/A—benign
rs1415397598:140,743,881C/T—likely benign
rs1894780238:140,744,009G/A—likely benign
rs1148018348:140,744,201G/A—likely benign
rs5522112608:140,744,205T/C—likely benign
rs14385097288:140,744,217C/T—uncertain significance
rs798773578:140,744,218G/T—uncertain significance
rs14896344798:140,744,221C/T—pathogenic
rs7501670298:140,744,223G/A—uncertain significance
rs7662463708:140,744,225G/A—likely benign
rs7537434858:140,744,228G/A—likely benign
rs21299352198:140,744,229A/C—uncertain significance
rs3699245578:140,744,244G/C—uncertain significance
rs7579987218:140,744,251C/T—uncertain significance
rs1125510698:140,744,252G/A—conflicting classifications of pathogenicity
rs1410670698:140,744,260C/T—conflicting classifications of pathogenicity
rs7463766608:140,744,261G/A—likely benign
rs1448807048:140,744,264G/A—likely benign
rs587405678:140,744,276G/T—conflicting classifications of pathogenicity
rs7621354748:140,744,281T/C—uncertain significance
rs13933915508:140,744,282G/C—uncertain significance
rs14597059328:140,744,284G/A—uncertain significance
rs7620760988:140,744,287C/T—uncertain significance
rs7594089228:140,744,288G/A—likely benign
rs2009634738:140,744,290C/T—uncertain significance
rs7578651608:140,744,291G/A—likely benign
rs13913264708:140,744,297G/C—uncertain significance
rs1409282078:140,744,302C/T—uncertain significance
rs1502009028:140,744,326C/T—conflicting classifications of pathogenicity
rs7462503078:140,744,327G/A—likely benign
rs1387786658:140,744,333C/T—likely benign
rs355789748:140,744,338C/T—conflicting classifications of pathogenicity
rs5555206028:140,744,339G/A—likely benign
rs3690749968:140,744,343C/T—uncertain significance
rs1474995938:140,744,344G/A—conflicting classifications of pathogenicity
rs12109926758:140,744,351C/A—likely benign
rs1117687458:140,744,352C/T—conflicting classifications of pathogenicity
rs5630502748:140,744,353G/A—conflicting classifications of pathogenicity
rs15637692308:140,744,354G/A—likely benign
rs5454803038:140,744,364C/T—uncertain significance
rs3766179208:140,744,365G/A—conflicting classifications of pathogenicity
rs24885134458:140,744,366C/T—uncertain significance
rs13933391058:140,744,374G/A—likely benign
rs2020421668:140,744,376C/T—likely benign
rs3710095878:140,744,377G/A—uncertain significance
rs7541720058:140,744,380C/T—uncertain significance
rs7692638688:140,744,381G/A—likely benign
rs7788001688:140,744,384G/T—uncertain significance
rs3743000078:140,744,387G/A—conflicting classifications of pathogenicity
rs12783628388:140,744,388C/A—uncertain significance
rs14820198238:140,744,393C/G—uncertain significance
rs5281705948:140,744,402C/T—likely benign
rs3763814838:140,744,403G/A—uncertain significance
rs7695434128:140,744,407C/T—uncertain significance
rs7669208668:140,744,413C/T—uncertain significance
rs5618292578:140,744,414G/A—likely benign
rs2001889688:140,744,415C/T—uncertain significance
rs13914312318:140,744,421C/T—uncertain significance
rs1440394208:140,744,423T/C—likely benign
rs1443837858:140,744,432G/A—likely benign
rs13098940898:140,744,434C/A—uncertain significance
rs7542416308:140,744,443C/T—uncertain significance

Showing 100 of 764 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.