CCDC63
coiled-coil domain containing 63
Summary
Predicted to be involved in cilium movement; outer dynein arm assembly; and spermatid development. Predicted to be active in axoneme. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs114761668 | 12:111,291,236 | G/T | — | uncertain significance |
| rs1318861061 | 12:111,291,242 | C/T | — | uncertain significance |
| rs2499690618 | 12:111,291,289 | G/C | — | uncertain significance |
| rs1029847714 | 12:111,291,351 | G/A | — | uncertain significance |
| rs76464604 | 12:111,293,470 | G/T | intron variant | — |
| rs2499701355 | 12:111,296,395 | A/C | — | uncertain significance |
| rs200140147 | 12:111,296,458 | C/T | — | uncertain significance |
| rs766133465 | 12:111,311,707 | C/T | — | uncertain significance |
| rs200569386 | 12:111,311,718 | C/T | — | uncertain significance |
| rs758717569 | 12:111,311,752 | C/A | — | uncertain significance |
| rs780746666 | 12:111,311,764 | T/C | — | uncertain significance |
| rs1407251218 | 12:111,317,780 | T/A | — | likely benign |
| rs147414240 | 12:111,317,839 | A/G | — | uncertain significance |
| rs376720183 | 12:111,317,849 | T/A | — | uncertain significance |
| rs1418308596 | 12:111,318,948 | T/G | — | uncertain significance |
| rs1163864985 | 12:111,318,949 | G/T | — | uncertain significance |
| rs775890946 | 12:111,318,956 | C/T | — | uncertain significance |
| rs115904738 | 12:111,318,957 | G/A | — | uncertain significance |
| rs151096735 | 12:111,321,908 | C/A | — | uncertain significance |
| rs778436400 | 12:111,321,993 | C/T | — | uncertain significance |
| rs149841694 | 12:111,322,002 | C/G | — | uncertain significance |
| rs1285696959 | 12:111,322,021 | G/C | — | uncertain significance |
| rs10849915 | 12:111,333,622 | T/C | intron variant | — |
| rs2499781294 | 12:111,336,744 | T/A | — | uncertain significance |
| rs760263993 | 12:111,336,789 | G/C | — | uncertain significance |
| rs760224067 | 12:111,336,879 | A/C | — | uncertain significance |
| rs758287561 | 12:111,336,903 | C/T | — | uncertain significance |
| rs10774610 | 12:111,340,243 | T/C | intron variant | — |
| rs200583861 | 12:111,342,398 | T/G | — | uncertain significance |
| rs762320804 | 12:111,342,442 | C/T | — | uncertain significance |
| rs772838782 | 12:111,342,461 | G/A | — | uncertain significance |
| rs372078813 | 12:111,342,496 | C/A | — | uncertain significance |
| rs769568156 | 12:111,342,550 | C/T | — | uncertain significance |
| rs75295329 | 12:111,344,621 | G/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.