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

Gene information from NCBI Gene. Variant classifications from ClinVar.