CCDC181
coiled-coil domain containing 181
Summary
Predicted to enable microtubule binding activity. Predicted to be located in manchette and sperm flagellum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs557950843 | 1:169,364,358 | C/T | — | uncertain significance |
| rs370391570 | 1:169,364,428 | G/A | — | uncertain significance |
| rs540305771 | 1:169,364,436 | C/A | — | uncertain significance |
| rs944149664 | 1:169,366,509 | T/C | — | uncertain significance |
| rs1481868919 | 1:169,366,529 | T/A | — | uncertain significance |
| rs773572519 | 1:169,366,534 | C/G | — | uncertain significance |
| rs143641979 | 1:169,366,558 | T/G | — | uncertain significance |
| rs773347654 | 1:169,366,598 | C/T | — | uncertain significance |
| rs7523660 | 1:169,372,224 | A/C | intron variant | — |
| rs559729404 | 1:169,375,991 | T/A | — | — |
| rs200950920 | 1:169,388,282 | C/G | — | uncertain significance |
| rs746280902 | 1:169,388,285 | T/G | — | uncertain significance |
| rs772291600 | 1:169,388,300 | T/C | — | uncertain significance |
| rs773104692 | 1:169,388,324 | T/G | — | uncertain significance |
| rs41272449 | 1:169,390,675 | T/G | — | uncertain significance |
| rs770791572 | 1:169,390,692 | A/G | — | uncertain significance |
| rs200412936 | 1:169,390,777 | G/A | — | uncertain significance |
| rs113005897 | 1:169,390,787 | T/C | — | likely benign |
| rs769331621 | 1:169,390,809 | G/A | — | uncertain significance |
| rs139902520 | 1:169,390,851 | G/A | — | likely benign |
| rs529244674 | 1:169,390,852 | T/C | — | likely benign |
| rs145998364 | 1:169,390,873 | C/T | — | uncertain significance |
| rs2526101026 | 1:169,390,911 | T/C | — | uncertain significance |
| rs2526102166 | 1:169,391,044 | A/G | — | uncertain significance |
| rs957226232 | 1:169,391,124 | A/G | — | uncertain significance |
| rs748928818 | 1:169,391,161 | T/C | — | uncertain significance |
| rs137855652 | 1:169,391,169 | T/C | — | uncertain significance |
| rs376964448 | 1:169,391,220 | C/T | — | uncertain significance |
| rs201319056 | 1:169,391,241 | G/A | — | uncertain significance |
| rs771323947 | 1:169,391,340 | T/C | — | uncertain significance |
| rs2526104383 | 1:169,391,343 | A/G | — | uncertain significance |
| rs772035986 | 1:169,391,358 | A/C | — | uncertain significance |
| rs1656506632 | 1:169,391,412 | A/G | — | uncertain significance |
| rs139153419 | 1:169,391,422 | T/C | — | uncertain significance |
| rs192068825 | 1:169,391,547 | G/A | — | uncertain significance |
| rs149997629 | 1:169,394,057 | T/C | — | uncertain significance |
| rs6673326 | 1:169,420,973 | G/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.