CCDC91
coiled-coil domain containing 91
Summary
Predicted to enable identical protein binding activity. Involved in Golgi to lysosome transport. Located in nucleoplasm and trans-Golgi network. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11049415 | 12:28,343,121 | C/T | coding sequence variant | — |
| rs11049418 | 12:28,345,087 | C/T | regulatory region variant | — |
| rs11049426 | 12:28,346,506 | A/C | upstream gene variant | — |
| rs11049431 | 12:28,347,382 | C/T | upstream gene variant | — |
| rs529602522 | 12:28,354,365 | C/T | — | — |
| rs11700039 | 12:28,354,391 | C/T | — | — |
| rs11049453 | 12:28,355,929 | G/A | regulatory region variant | — |
| rs71452082 | 12:28,374,580 | C/T | — | — |
| rs1871152 | 12:28,379,826 | G/T | — | — |
| rs79712894 | 12:28,392,333 | A/C | — | — |
| rs1979679 | 12:28,406,515 | T/C | regulatory region variant | — |
| rs189064624 | 12:28,420,713 | A/C | intron variant | — |
| rs370320187 | 12:28,420,738 | G/A | — | — |
| rs148253596 | 12:28,422,926 | A/C | intron variant | — |
| rs11049508 | 12:28,442,566 | G/A | intron variant | — |
| rs79395932 | 12:28,451,311 | C/A | — | — |
| rs7964793 | 12:28,451,709 | G/C | — | — |
| rs368981349 | 12:28,458,630 | G/A | — | likely benign |
| rs1331277514 | 12:28,459,694 | C/T | — | uncertain significance |
| rs2541063859 | 12:28,459,703 | A/G | — | uncertain significance |
| rs143087318 | 12:28,459,769 | A/G | — | benign |
| rs374805167 | 12:28,459,825 | A/G | — | uncertain significance |
| rs1938894031 | 12:28,460,647 | G/A | — | uncertain significance |
| rs10843151 | 12:28,471,319 | G/A | downstream gene variant | — |
| rs11049529 | 12:28,471,504 | C/A | — | — |
| rs11049539 | 12:28,488,886 | A/T | intron variant | — |
| rs781406194 | 12:28,515,437 | G/T | — | uncertain significance |
| rs78500430 | 12:28,522,761 | C/T | regulatory region variant | — |
| rs187686499 | 12:28,531,178 | T/C | regulatory region variant | — |
| rs2638953 | 12:28,534,415 | G/T | — | — |
| rs1257741 | 12:28,534,569 | G/C | intron variant | — |
| rs146304266 | 12:28,544,291 | A/G | — | uncertain significance |
| rs201539743 | 12:28,544,301 | T/C | — | uncertain significance |
| rs750535226 | 12:28,544,327 | G/C | — | uncertain significance |
| rs552231030 | 12:28,547,845 | A/G | — | — |
| rs10843164 | 12:28,569,714 | T/C | intron variant | — |
| rs542653660 | 12:28,570,571 | T/C | — | — |
| rs11049587 | 12:28,571,023 | C/A | intron variant | — |
| rs10843169 | 12:28,582,984 | T/A | intron variant | — |
| rs11049598 | 12:28,589,093 | T/C | intron variant | — |
| rs11049611 | 12:28,600,244 | C/A | — | — |
| rs1949729725 | 12:28,603,102 | G/C | — | uncertain significance |
| rs201390676 | 12:28,603,122 | C/A | — | uncertain significance |
| rs772462544 | 12:28,603,311 | A/T | — | uncertain significance |
| rs760444503 | 12:28,605,450 | G/A | — | likely benign |
| rs2542969631 | 12:28,605,537 | G/T | — | uncertain significance |
| rs1417495173 | 12:28,637,022 | G/A | — | uncertain significance |
| rs575535667 | 12:28,637,061 | G/C | — | uncertain significance |
| rs764100361 | 12:28,637,064 | A/T | — | uncertain significance |
| rs1486938125 | 12:28,637,083 | A/G | — | uncertain significance |
| rs61731729 | 12:28,637,090 | C/A | — | benign |
| rs11049667 | 12:28,649,875 | A/G | intron variant | — |
| rs150260458 | 12:28,656,487 | T/G | — | — |
| rs11049689 | 12:28,672,110 | G/A | intron variant | — |
| rs1469075683 | 12:28,702,078 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.