CCDC93
CCC complex scaffolding subunit CCDC93
Summary
Involved in Golgi to plasma membrane transport and endocytic recycling. Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1319780623 | 2:118,677,932 | G/A | — | uncertain significance |
| rs779574804 | 2:118,677,966 | G/A | — | uncertain significance |
| rs150097723 | 2:118,683,279 | G/A | intron variant | — |
| rs146962013 | 2:118,684,133 | A/G | intron variant | — |
| rs1191728790 | 2:118,688,617 | T/C | — | uncertain significance |
| rs140975342 | 2:118,693,117 | C/T | — | uncertain significance |
| rs138708100 | 2:118,693,132 | C/T | — | uncertain significance |
| rs372727967 | 2:118,693,133 | G/A | — | uncertain significance |
| rs72834384 | 2:118,693,249 | C/T | downstream gene variant | — |
| rs969718782 | 2:118,696,607 | C/T | — | uncertain significance |
| rs2466896344 | 2:118,696,682 | C/T | — | uncertain significance |
| rs148434878 | 2:118,698,771 | G/A | — | uncertain significance |
| rs767245569 | 2:118,698,788 | C/T | — | uncertain significance |
| rs747392111 | 2:118,698,840 | G/A | — | uncertain significance |
| rs1678790603 | 2:118,701,629 | C/T | — | uncertain significance |
| rs142085524 | 2:118,701,647 | G/A | — | uncertain significance |
| rs751983591 | 2:118,706,917 | C/G | — | uncertain significance |
| rs753979004 | 2:118,709,959 | G/A | — | uncertain significance |
| rs17511616 | 2:118,713,877 | T/C | intron variant | — |
| rs745363342 | 2:118,715,996 | C/T | — | uncertain significance |
| rs60716475 | 2:118,720,178 | C/T | intron variant | — |
| rs72838016 | 2:118,729,582 | G/A | intron variant | — |
| rs372750359 | 2:118,731,498 | C/T | — | uncertain significance |
| rs140577157 | 2:118,731,566 | C/T | — | uncertain significance |
| rs1254707617 | 2:118,732,433 | T/C | — | uncertain significance |
| rs577490713 | 2:118,732,443 | C/T | — | uncertain significance |
| rs758476502 | 2:118,732,825 | C/T | — | uncertain significance |
| rs17512204 | 2:118,732,831 | G/A | — | benign |
| rs368632876 | 2:118,732,837 | G/A | — | uncertain significance |
| rs200757900 | 2:118,743,591 | G/C | — | uncertain significance |
| rs773023570 | 2:118,743,614 | C/T | — | uncertain significance |
| rs2466851144 | 2:118,743,645 | C/T | — | uncertain significance |
| rs540747651 | 2:118,743,804 | G/A | — | — |
| rs55703214 | 2:118,747,026 | T/C | intron variant | — |
| rs2466876652 | 2:118,753,076 | A/C | — | uncertain significance |
| rs765185486 | 2:118,753,077 | T/C | — | uncertain significance |
| rs753072596 | 2:118,753,892 | T/C | — | uncertain significance |
| rs777697897 | 2:118,753,926 | G/C | — | uncertain significance |
| rs11684454 | 2:118,763,068 | G/A | intron variant | — |
| rs375816525 | 2:118,764,313 | G/A | — | uncertain significance |
| rs1335593085 | 2:118,766,188 | A/G | — | uncertain significance |
| rs1676940793 | 2:118,766,227 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.