TRAPPC10
trafficking protein particle complex subunit 10
Summary
The protein encoded by this gene is a transmembrane protein found in the cis-Golgi complex. The encoded protein is part of the multisubunit transport protein particle (TRAPP) complex and may be involved in vesicular transport from the endoplasmic reticulum to the Golgi. Mutations in this gene could be responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy, or for autoimmune polyglandular disease type 1. [provided by RefSeq, Jul 2008]
Known Variants85 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2517113494 | 21:45,432,384 | T/C | — | likely benign |
| rs1051415355 | 21:45,432,388 | A/G | — | uncertain significance |
| rs201880764 | 21:45,432,394 | C/T | — | uncertain significance |
| rs1480303913 | 21:45,432,403 | C/T | — | uncertain significance |
| rs192925482 | 21:45,447,221 | A/G | intron variant | — |
| rs530457040 | 21:45,452,011 | C/T | — | uncertain significance |
| rs749049232 | 21:45,452,025 | C/T | — | uncertain significance |
| rs201213914 | 21:45,452,058 | G/C | — | likely benign |
| rs145481876 | 21:45,472,267 | A/T | — | uncertain significance |
| rs758948147 | 21:45,472,269 | G/A | — | uncertain significance |
| rs779207334 | 21:45,472,355 | C/A | — | uncertain significance |
| rs779083954 | 21:45,475,637 | G/A | — | uncertain significance |
| rs760489413 | 21:45,475,736 | G/C | — | uncertain significance |
| rs1363370685 | 21:45,479,015 | A/G | — | uncertain significance |
| rs376972497 | 21:45,479,039 | A/G | — | uncertain significance |
| rs775590351 | 21:45,479,089 | G/T | — | uncertain significance |
| rs763070293 | 21:45,479,092 | G/A | — | uncertain significance |
| rs775859051 | 21:45,483,548 | G/A | — | uncertain significance |
| rs2517484633 | 21:45,483,568 | C/T | — | likely pathogenic |
| rs2517485428 | 21:45,483,625 | G/A | — | uncertain significance |
| rs144074948 | 21:45,494,290 | G/A | — | uncertain significance |
| rs148635981 | 21:45,494,326 | G/A | — | uncertain significance |
| rs754325294 | 21:45,494,969 | A/T | — | uncertain significance |
| rs372581600 | 21:45,497,592 | A/T | — | uncertain significance |
| rs903583933 | 21:45,497,593 | T/C | — | uncertain significance |
| rs756095616 | 21:45,497,664 | A/C | — | uncertain significance |
| rs755861895 | 21:45,499,474 | T/C | — | uncertain significance |
| rs145051918 | 21:45,499,479 | C/T | — | uncertain significance |
| rs148086257 | 21:45,499,514 | C/T | — | benign |
| rs2517610611 | 21:45,499,560 | C/G | — | uncertain significance |
| rs767157215 | 21:45,499,573 | G/A | — | uncertain significance |
| rs371689506 | 21:45,499,951 | C/T | — | uncertain significance |
| rs776419319 | 21:45,499,955 | A/G | — | uncertain significance |
| rs375606142 | 21:45,499,994 | C/T | — | uncertain significance |
| rs371264768 | 21:45,502,686 | C/T | — | uncertain significance |
| rs766656453 | 21:45,502,740 | G/A | — | uncertain significance |
| rs202139853 | 21:45,502,779 | A/G | — | likely benign |
| rs141930416 | 21:45,502,958 | G/C | — | uncertain significance |
| rs532659058 | 21:45,502,992 | A/G | — | uncertain significance |
| rs774992912 | 21:45,503,111 | G/T | — | likely benign |
| rs2071152 | 21:45,503,121 | G/A | missense variant | — |
| rs748907606 | 21:45,504,066 | G/C | — | uncertain significance |
| rs751783122 | 21:45,504,136 | C/T | — | uncertain significance |
| rs756976242 | 21:45,506,687 | C/G | — | uncertain significance |
| rs1336299336 | 21:45,506,722 | C/G | — | uncertain significance |
| rs139545421 | 21:45,506,743 | C/T | — | uncertain significance |
| rs2038173557 | 21:45,506,784 | G/A | — | uncertain significance |
| rs765597290 | 21:45,506,787 | A/G | — | uncertain significance |
| rs746836367 | 21:45,506,836 | C/T | — | uncertain significance |
| rs2038239715 | 21:45,507,594 | G/T | — | uncertain significance |
| rs759992126 | 21:45,507,598 | C/T | — | uncertain significance |
| rs145010758 | 21:45,507,618 | G/A | — | uncertain significance |
| rs577569754 | 21:45,507,622 | A/G | — | uncertain significance |
| rs115506565 | 21:45,507,663 | G/A | — | likely benign |
| rs1277338191 | 21:45,507,711 | C/G | — | uncertain significance |
| rs142950110 | 21:45,507,731 | G/C | — | uncertain significance |
| rs772573780 | 21:45,507,772 | A/G | — | uncertain significance |
| rs764930393 | 21:45,507,784 | G/A | — | likely benign |
| rs60541190 | 21:45,507,818 | G/T | — | benign |
| rs9979882 | 21:45,508,682 | G/T | — | — |
| rs2038452747 | 21:45,509,726 | T/A | — | uncertain significance |
| rs2038452898 | 21:45,509,730 | C/T | — | pathogenic |
| rs2038454309 | 21:45,509,750 | G/A | — | uncertain significance |
| rs146810291 | 21:45,509,771 | G/A | — | uncertain significance |
| rs140629527 | 21:45,509,786 | A/G | — | uncertain significance |
| rs549161584 | 21:45,511,254 | T/A | — | — |
| rs386352376 | 21:45,511,862 | A/G | — | uncertain significance |
| rs145633595 | 21:45,511,880 | G/T | — | uncertain significance |
| rs138266841 | 21:45,511,922 | T/C | — | uncertain significance |
| rs143166326 | 21:45,513,974 | G/A | — | likely benign |
| rs1424410540 | 21:45,514,089 | A/C | — | uncertain significance |
| rs1179604644 | 21:45,518,291 | C/A | — | likely pathogenic |
| rs767726096 | 21:45,518,346 | T/G | — | uncertain significance |
| rs187027731 | 21:45,522,290 | T/G | upstream gene variant | — |
| rs146859911 | 21:45,522,725 | C/G | — | uncertain significance |
| rs1283342940 | 21:45,522,730 | C/T | — | uncertain significance |
| rs372582114 | 21:45,522,736 | A/G | — | uncertain significance |
| rs752419678 | 21:45,522,752 | T/C | — | uncertain significance |
| rs1479456990 | 21:45,522,753 | G/A | — | uncertain significance |
| rs1029148375 | 21:45,523,191 | G/A | — | uncertain significance |
| rs1324294279 | 21:45,523,228 | C/T | — | likely benign |
| rs2039104204 | 21:45,523,302 | C/T | — | uncertain significance |
| rs1211999287 | 21:45,523,305 | C/T | — | uncertain significance |
| rs767191085 | 21:45,523,306 | G/A | — | uncertain significance |
| rs755879812 | 21:45,523,321 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.