COPG1
coat protein complex I subunit gamma 1
Summary
Predicted to enable structural molecule activity. Predicted to be involved in several processes, including Golgi vesicle transport; establishment of Golgi localization; and organelle transport along microtubule. Located in Golgi apparatus. Implicated in immunodeficiency 128. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2530334014 | 3:128,968,566 | T/C | — | uncertain significance |
| rs4927953 | 3:128,971,113 | T/C | — | benign |
| rs1428685967 | 3:128,971,145 | C/T | — | uncertain significance |
| rs1939716871 | 3:128,971,196 | A/C | — | uncertain significance |
| rs764263230 | 3:128,971,473 | A/T | — | uncertain significance |
| rs372813357 | 3:128,971,485 | C/T | — | uncertain significance |
| rs554697382 | 3:128,971,486 | G/A | — | likely benign |
| rs766752287 | 3:128,971,728 | C/T | — | uncertain significance |
| rs140716300 | 3:128,971,732 | G/A | — | uncertain significance |
| rs375731470 | 3:128,971,747 | C/T | — | uncertain significance |
| rs73202214 | 3:128,971,751 | C/T | — | likely benign |
| rs957644685 | 3:128,971,767 | A/C | — | uncertain significance |
| rs1256193425 | 3:128,973,553 | C/T | — | likely benign |
| rs570175744 | 3:128,973,557 | G/C | — | uncertain significance |
| rs1439062784 | 3:128,973,829 | G/T | — | uncertain significance |
| rs1478139150 | 3:128,973,892 | T/A | — | uncertain significance |
| rs4927912 | 3:128,973,978 | A/C | — | benign |
| rs768520281 | 3:128,976,375 | G/A | — | uncertain significance |
| rs907902971 | 3:128,976,395 | A/G | — | uncertain significance |
| rs4927910 | 3:128,976,396 | T/C | — | benign |
| rs62266876 | 3:128,976,451 | C/G | — | likely benign |
| rs77129536 | 3:128,976,693 | G/A | — | benign |
| rs199838147 | 3:128,979,205 | G/T | — | uncertain significance |
| rs775881986 | 3:128,979,226 | G/A | — | uncertain significance |
| rs6802965 | 3:128,979,256 | C/G | — | benign |
| rs756483626 | 3:128,979,547 | C/T | — | uncertain significance |
| rs62266877 | 3:128,980,032 | G/A | intron variant | — |
| rs892932468 | 3:128,984,392 | G/T | — | uncertain significance |
| rs139673651 | 3:128,984,411 | G/A | — | uncertain significance |
| rs759220825 | 3:128,984,479 | C/T | — | uncertain significance |
| rs755024721 | 3:128,984,587 | C/G | — | uncertain significance |
| rs143413694 | 3:128,985,923 | A/G | — | uncertain significance |
| rs61128088 | 3:128,986,715 | A/C | — | benign |
| rs2530376826 | 3:128,986,788 | T/C | — | uncertain significance |
| rs2530376855 | 3:128,986,806 | T/A | — | uncertain significance |
| rs781497550 | 3:128,986,815 | G/A | — | uncertain significance |
| rs1408217422 | 3:128,986,827 | A/G | — | uncertain significance |
| rs572845400 | 3:128,987,440 | C/T | — | uncertain significance |
| rs370345221 | 3:128,987,448 | G/A | — | uncertain significance |
| rs930091928 | 3:128,987,470 | C/T | — | uncertain significance |
| rs10934875 | 3:128,987,730 | G/A | — | benign |
| rs10934876 | 3:128,987,899 | T/A | — | benign |
| rs758465512 | 3:128,990,622 | C/G | — | uncertain significance |
| rs770999835 | 3:128,990,636 | C/T | — | uncertain significance |
| rs776568797 | 3:128,990,637 | G/A | — | uncertain significance |
| rs1054228191 | 3:128,990,651 | C/T | — | uncertain significance |
| rs779788008 | 3:128,990,664 | C/T | — | uncertain significance |
| rs1199837030 | 3:128,990,687 | G/A | — | uncertain significance |
| rs148765285 | 3:128,990,697 | C/T | — | uncertain significance |
| rs563330778 | 3:128,990,698 | G/A | — | likely benign |
| rs116159732 | 3:128,991,036 | C/T | intron variant | — |
| rs755324186 | 3:128,991,129 | G/A | — | uncertain significance |
| rs756754245 | 3:128,991,187 | G/A | — | uncertain significance |
| rs745877931 | 3:128,991,746 | T/C | — | uncertain significance |
| rs6762578 | 3:128,992,047 | G/A | intron variant | — |
| rs1940236299 | 3:128,993,687 | G/C | — | uncertain significance |
| rs776164953 | 3:128,993,736 | A/C | — | uncertain significance |
| rs1448763391 | 3:128,993,741 | G/A | — | uncertain significance |
| rs374887499 | 3:128,993,779 | G/T | — | uncertain significance |
| rs1177089300 | 3:128,994,043 | T/C | — | uncertain significance |
| rs145582621 | 3:128,994,075 | C/G | — | uncertain significance |
| rs746757757 | 3:128,994,100 | C/T | — | uncertain significance |
| rs2530390068 | 3:128,994,130 | T/C | — | uncertain significance |
| rs777024879 | 3:128,996,168 | G/T | — | uncertain significance |
| rs143625930 | 3:128,996,169 | C/T | — | uncertain significance |
| rs777779290 | 3:128,996,226 | G/A | — | uncertain significance |
| rs749354777 | 3:128,996,232 | C/A | — | uncertain significance |
| rs142227526 | 3:128,996,243 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.