CCDC81
coiled-coil domain containing 81
Summary
Located in centrosome; ciliary basal body; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200126484 | 11:86,098,568 | T/C | — | uncertain significance |
| rs143584200 | 11:86,098,573 | G/C | — | uncertain significance |
| rs749864427 | 11:86,098,616 | G/A | — | uncertain significance |
| rs866033325 | 11:86,098,652 | T/G | — | uncertain significance |
| rs773387703 | 11:86,098,657 | A/G | — | uncertain significance |
| rs1007968060 | 11:86,098,699 | A/G | — | uncertain significance |
| rs1403287205 | 11:86,103,597 | G/A | — | uncertain significance |
| rs571570699 | 11:86,103,601 | C/T | — | uncertain significance |
| rs578071215 | 11:86,103,691 | G/A | — | uncertain significance |
| rs2496281740 | 11:86,103,712 | A/C | — | uncertain significance |
| rs759923255 | 11:86,103,724 | C/T | — | uncertain significance |
| rs2496281872 | 11:86,103,754 | G/T | — | uncertain significance |
| rs2496281880 | 11:86,103,755 | A/T | — | uncertain significance |
| rs1416959632 | 11:86,103,775 | G/C | — | uncertain significance |
| rs1319474820 | 11:86,103,787 | A/T | — | uncertain significance |
| rs1356121542 | 11:86,103,801 | A/G | — | uncertain significance |
| rs757572257 | 11:86,103,802 | T/C | — | uncertain significance |
| rs762925420 | 11:86,111,751 | A/T | — | uncertain significance |
| rs609443 | 11:86,111,753 | A/G | — | uncertain significance |
| rs370882638 | 11:86,111,818 | G/A | — | uncertain significance |
| rs2496309579 | 11:86,118,660 | T/C | — | uncertain significance |
| rs748385926 | 11:86,119,223 | A/G | — | likely benign |
| rs776461381 | 11:86,119,242 | A/T | — | uncertain significance |
| rs367557953 | 11:86,119,247 | G/C | — | uncertain significance |
| rs969899330 | 11:86,119,263 | T/C | — | uncertain significance |
| rs138592676 | 11:86,123,451 | G/A | — | uncertain significance |
| rs766513360 | 11:86,123,466 | C/T | — | uncertain significance |
| rs767224921 | 11:86,125,894 | A/C | — | uncertain significance |
| rs549422279 | 11:86,125,986 | C/T | — | — |
| rs773100251 | 11:86,126,185 | G/C | — | uncertain significance |
| rs145499523 | 11:86,126,217 | T/C | — | uncertain significance |
| rs1188630520 | 11:86,126,247 | A/C | — | uncertain significance |
| rs773477496 | 11:86,126,250 | T/C | — | uncertain significance |
| rs2496322794 | 11:86,126,251 | G/T | — | uncertain significance |
| rs772004217 | 11:86,126,322 | G/A | — | uncertain significance |
| rs760460166 | 11:86,126,330 | C/A | — | uncertain significance |
| rs2496329934 | 11:86,130,999 | A/C | — | uncertain significance |
| rs150352880 | 11:86,131,002 | G/A | — | uncertain significance |
| rs138508969 | 11:86,131,094 | C/T | — | uncertain significance |
| rs113010452 | 11:86,133,626 | A/G | — | uncertain significance |
| rs992209356 | 11:86,133,645 | A/G | — | uncertain significance |
| rs141550907 | 11:86,133,660 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.