CCDC92
coiled-coil domain containing 92
Summary
Enables identical protein binding activity. Predicted to be involved in innate immune response and regulation of defense response to virus. Located in centriole; centrosome; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs774556689 | 12:124,421,664 | C/T | — | uncertain significance |
| rs777802261 | 12:124,421,685 | C/T | — | uncertain significance |
| rs1164797678 | 12:124,421,705 | G/A | — | uncertain significance |
| rs371993242 | 12:124,421,720 | C/T | — | uncertain significance |
| rs962982196 | 12:124,421,732 | C/G | — | uncertain significance |
| rs750311604 | 12:124,421,737 | G/T | — | uncertain significance |
| rs375219968 | 12:124,421,781 | C/T | — | likely benign |
| rs575729715 | 12:124,421,790 | C/T | — | uncertain significance |
| rs367836688 | 12:124,421,796 | C/T | — | uncertain significance |
| rs371367334 | 12:124,421,801 | G/C | — | uncertain significance |
| rs1047655593 | 12:124,421,802 | G/C | — | uncertain significance |
| rs762582864 | 12:124,421,811 | C/T | — | uncertain significance |
| rs760478976 | 12:124,421,841 | C/T | — | uncertain significance |
| rs200277506 | 12:124,421,900 | C/T | — | uncertain significance |
| rs773223947 | 12:124,421,919 | T/C | — | uncertain significance |
| rs1311068677 | 12:124,421,924 | G/A | — | uncertain significance |
| rs200976444 | 12:124,421,993 | C/T | — | uncertain significance |
| rs150284078 | 12:124,421,999 | G/A | — | uncertain significance |
| rs781130374 | 12:124,422,099 | T/G | — | uncertain significance |
| rs1254245039 | 12:124,422,228 | C/T | — | uncertain significance |
| rs184378821 | 12:124,422,300 | C/T | — | uncertain significance |
| rs201517947 | 12:124,422,346 | C/A | — | uncertain significance |
| rs11057401 | 12:124,427,306 | T/A | missense variant | — |
| rs769500480 | 12:124,427,915 | G/A | — | uncertain significance |
| rs753848940 | 12:124,427,924 | C/T | — | uncertain significance |
| rs376515224 | 12:124,427,959 | C/T | — | uncertain significance |
| rs769441748 | 12:124,427,989 | C/T | — | uncertain significance |
| rs7132655 | 12:124,438,973 | G/C | intron variant | — |
| rs6488913 | 12:124,445,569 | C/G | coding sequence variant | — |
| rs11833002 | 12:124,446,616 | G/A | downstream gene variant | — |
| rs3789967 | 12:124,447,339 | T/G | coding sequence variant | — |
| rs80270210 | 12:124,447,397 | G/T | — | — |
| rs55990776 | 12:124,447,466 | A/G | downstream gene variant | — |
| rs1882491 | 12:124,454,235 | T/C | upstream gene variant | — |
| rs192451380 | 12:124,457,223 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.