CCDC82
coiled-coil domain containing 82
Summary
Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1864497392 | 11:96,092,276 | A/G | — | uncertain significance |
| rs374755193 | 11:96,092,311 | C/T | — | uncertain significance |
| rs1400059466 | 11:96,092,312 | G/A | — | uncertain significance |
| rs143699327 | 11:96,092,315 | T/G | — | uncertain significance |
| rs56015144 | 11:96,096,137 | T/A | — | — |
| rs1457199867 | 11:96,098,155 | G/A | — | uncertain significance |
| rs139262571 | 11:96,098,183 | C/G | — | uncertain significance |
| rs371250562 | 11:96,098,230 | A/G | — | likely benign |
| rs753848269 | 11:96,098,305 | C/T | — | uncertain significance |
| rs934472910 | 11:96,104,184 | T/C | — | uncertain significance |
| rs751861324 | 11:96,104,223 | C/T | — | uncertain significance |
| rs2496457793 | 11:96,106,578 | T/C | — | uncertain significance |
| rs7118648 | 11:96,108,428 | T/G | — | — |
| rs763390036 | 11:96,116,544 | T/C | — | uncertain significance |
| rs140141313 | 11:96,116,556 | C/T | — | uncertain significance |
| rs1480084121 | 11:96,116,634 | A/C | — | uncertain significance |
| rs368959188 | 11:96,116,637 | C/T | — | uncertain significance |
| rs148541924 | 11:96,117,149 | G/A | — | uncertain significance |
| rs752598700 | 11:96,117,158 | G/A | — | uncertain significance |
| rs1279565577 | 11:96,117,181 | T/C | — | uncertain significance |
| rs759225013 | 11:96,117,259 | C/A | — | uncertain significance |
| rs757309380 | 11:96,117,281 | G/A | — | uncertain significance |
| rs761854053 | 11:96,117,371 | T/C | — | uncertain significance |
| rs141347770 | 11:96,117,376 | C/T | — | uncertain significance |
| rs758691852 | 11:96,117,377 | G/A | — | conflicting classifications of pathogenicity |
| rs369937047 | 11:96,117,437 | C/T | — | uncertain significance |
| rs533065669 | 11:96,117,483 | T/G | — | uncertain significance |
| rs2496610832 | 11:96,117,523 | A/G | — | likely benign |
| rs779657939 | 11:96,117,526 | T/C | — | uncertain significance |
| rs75857759 | 11:96,117,590 | T/C | — | benign |
| rs2496614041 | 11:96,117,623 | T/C | — | uncertain significance |
| rs2496614969 | 11:96,117,647 | T/C | — | uncertain significance |
| rs774861008 | 11:96,117,697 | C/G | — | uncertain significance |
| rs1306561800 | 11:96,117,750 | C/A | — | uncertain significance |
| rs2496621265 | 11:96,117,794 | T/C | — | uncertain significance |
| rs61746142 | 11:96,117,812 | T/C | — | likely benign |
| rs1866090527 | 11:96,117,845 | G/A | — | likely pathogenic |
| rs138210164 | 11:96,117,881 | T/C | — | uncertain significance |
| rs373680223 | 11:96,117,886 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.