TRAPPC8

trafficking protein particle complex subunit 8

Summary

Involved in Golgi organization and collagen biosynthetic process. Part of TRAPP complex. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants83 total

rsidPosition (GRCh37)AllelesClassClinVar
rs20062816518:29,410,777C/G—uncertain significance
rs36847835218:29,410,791G/A—uncertain significance
rs14015791518:29,410,801C/A—uncertain significance
rs20219631518:29,410,813G/C—uncertain significance
rs251109241218:29,410,882T/G—uncertain significance
rs3475379218:29,410,900A/G—uncertain significance
rs148783620618:29,410,948C/T—uncertain significance
rs52928036218:29,412,101T/C—uncertain significance
rs14970803718:29,419,382T/C—likely benign
rs251114608418:29,426,710C/T—uncertain significance
rs76672671318:29,426,716G/A—uncertain significance
rs13901899518:29,426,726T/C—likely benign
rs54386821518:29,428,104C/T——
rs75377709618:29,429,593T/C—uncertain significance
rs77029897018:29,429,629G/T—uncertain significance
rs15023802818:29,429,633G/C—uncertain significance
rs122438033718:29,432,575C/T—uncertain significance
rs77833325318:29,433,818T/C—uncertain significance
rs77112867218:29,433,827G/T—uncertain significance
rs251117273318:29,433,862C/T—uncertain significance
rs75626190418:29,433,908T/C—uncertain significance
rs159861250918:29,435,640C/T—uncertain significance
rs75759752818:29,435,667C/T—uncertain significance
rs14395604418:29,435,668T/A—uncertain significance
rs78025214418:29,435,700T/C—uncertain significance
rs251118742518:29,437,575G/A—uncertain significance
rs251118766218:29,437,609C/T—uncertain significance
rs251118855618:29,437,690A/C—uncertain significance
rs77464273218:29,437,732C/T—uncertain significance
rs11282713318:29,437,741C/T—uncertain significance
rs97792307418:29,437,786G/T—uncertain significance
rs217056218:29,437,830C/T—uncertain significance
rs11446555818:29,444,581G/A—benign
rs14915584618:29,444,633C/T—uncertain significance
rs75878419318:29,444,654G/C—uncertain significance
rs37525997018:29,444,675T/C—uncertain significance
rs52980052718:29,444,700C/T—uncertain significance
rs77047679218:29,444,725C/T—uncertain significance
rs13834810618:29,446,802T/C—benign
rs86798214018:29,446,832G/A—uncertain significance
rs75034853418:29,450,431A/G—likely benign
rs20145867918:29,450,933T/G—uncertain significance
rs14531819018:29,450,945T/C—uncertain significance
rs14868332018:29,450,985C/T—uncertain significance
rs74699369418:29,453,398G/A—uncertain significance
rs77278657718:29,453,441T/C—uncertain significance
rs74539750218:29,454,561T/C—uncertain significance
rs128253768318:29,454,564G/C—uncertain significance
rs77470465818:29,454,576A/G—uncertain significance
rs126074947818:29,470,771A/G—uncertain significance
rs93947749918:29,477,847C/T—uncertain significance
rs19971896018:29,477,850T/C—uncertain significance
rs94624186718:29,487,439T/A—uncertain significance
rs13796884718:29,487,446T/C—uncertain significance
rs37651754518:29,487,568G/A—uncertain significance
rs76209093918:29,488,749T/C—uncertain significance
rs134628928118:29,488,772G/A—uncertain significance
rs86714381518:29,488,793C/T—uncertain significance
rs144991245418:29,488,845T/G—uncertain significance
rs14425951918:29,488,850C/A—uncertain significance
rs77344613718:29,488,892T/A—uncertain significance
rs251136927018:29,488,908T/C—uncertain significance
rs75013850718:29,488,973T/A—uncertain significance
rs75181020418:29,489,684T/C—uncertain significance
rs20147197418:29,489,705G/C—uncertain significance
rs37105649218:29,493,335G/C—uncertain significance
rs251138206118:29,493,409T/A—uncertain significance
rs77753406518:29,493,411C/T—uncertain significance
rs251138210418:29,493,428T/A—uncertain significance
rs203700292918:29,493,438C/A—uncertain significance
rs251139009618:29,496,332G/C—uncertain significance
rs251139056818:29,496,407T/C—uncertain significance
rs251085648918:29,511,296G/C—uncertain significance
rs75535853218:29,511,331T/G—uncertain significance
rs3429253318:29,511,423T/C—benign
rs91490031318:29,511,472G/T—uncertain significance
rs146861857218:29,511,484G/A—uncertain significance
rs15080467318:29,512,401A/Cintron variant—
rs11174971518:29,522,555G/Acoding sequence variant—
rs74592209118:29,522,586G/A—uncertain significance
rs37486594318:29,522,588G/C—uncertain significance
rs117814700718:29,522,645G/A—uncertain significance
rs57622554518:29,524,613G/A——

Gene information from NCBI Gene. Variant classifications from ClinVar.