CFAP77
cilia and flagella associated protein 77
Summary
Predicted to be involved in flagellated sperm motility. Located in axonemal microtubule. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1479188235 | 9:135,285,675 | G/C | — | uncertain significance |
| rs200191178 | 9:135,285,690 | T/C | — | likely benign |
| rs758714879 | 9:135,285,722 | C/A | — | uncertain significance |
| rs372053390 | 9:135,285,726 | G/T | — | uncertain significance |
| rs143242576 | 9:135,285,779 | A/C | — | uncertain significance |
| rs200963844 | 9:135,285,791 | A/T | — | uncertain significance |
| rs528634693 | 9:135,285,809 | G/A | — | uncertain significance |
| rs79768058 | 9:135,311,668 | T/C | intron variant | — |
| rs569434 | 9:135,344,407 | G/T | — | — |
| rs758203447 | 9:135,357,749 | C/T | — | uncertain significance |
| rs767763161 | 9:135,357,755 | A/G | — | uncertain significance |
| rs148397666 | 9:135,374,161 | T/C | — | uncertain significance |
| rs781291713 | 9:135,374,172 | G/A | — | uncertain significance |
| rs145957603 | 9:135,374,806 | G/A | — | uncertain significance |
| rs750950057 | 9:135,374,816 | G/A | — | uncertain significance |
| rs769398138 | 9:135,374,836 | C/T | — | uncertain significance |
| rs150368747 | 9:135,374,839 | G/A | — | uncertain significance |
| rs201351590 | 9:135,374,854 | G/A | — | uncertain significance |
| rs1267048021 | 9:135,374,920 | G/C | — | uncertain significance |
| rs192787303 | 9:135,380,769 | C/T | intron variant | — |
| rs114869957 | 9:135,389,297 | T/A | intron variant | — |
| rs117783327 | 9:135,400,689 | G/T | intron variant | — |
| rs182716958 | 9:135,413,022 | C/T | — | uncertain significance |
| rs766142719 | 9:135,418,388 | C/T | — | uncertain significance |
| rs376871470 | 9:135,418,414 | C/T | — | uncertain significance |
| rs761872564 | 9:135,418,425 | C/G | — | uncertain significance |
| rs143925270 | 9:135,428,552 | G/A | intron variant | — |
| rs187751347 | 9:135,429,965 | C/T | intron variant | — |
| rs140858884 | 9:135,447,781 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.