CFAP206
cilia and flagella associated protein 206
Summary
Predicted to be involved in regulation of cilium beat frequency; regulation of flagellated sperm motility; and sperm axoneme assembly. Predicted to be located in A axonemal microtubule and motile cilium. Predicted to be part of radial spoke. Predicted to be active in axoneme and ciliary basal body. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs377497011 | 6:88,119,585 | A/G | — | uncertain significance |
| rs1389023986 | 6:88,119,639 | G/T | — | uncertain significance |
| rs535296260 | 6:88,119,663 | A/G | — | uncertain significance |
| rs377042908 | 6:88,123,597 | G/A | — | uncertain significance |
| rs1475908398 | 6:88,125,481 | G/T | — | uncertain significance |
| rs769176100 | 6:88,125,502 | G/A | — | uncertain significance |
| rs542071458 | 6:88,126,426 | C/T | — | uncertain significance |
| rs367568626 | 6:88,126,458 | C/T | — | uncertain significance |
| rs780934340 | 6:88,126,459 | G/A | — | uncertain significance |
| rs267601153 | 6:88,127,953 | C/T | — | uncertain significance |
| rs140079201 | 6:88,127,994 | C/T | — | uncertain significance |
| rs142943998 | 6:88,127,995 | G/A | — | likely benign |
| rs1452052996 | 6:88,128,016 | C/G | — | uncertain significance |
| rs761405774 | 6:88,128,068 | G/C | — | uncertain significance |
| rs750840329 | 6:88,128,088 | C/T | — | uncertain significance |
| rs766616091 | 6:88,128,094 | A/G | — | uncertain significance |
| rs6912958 | 6:88,133,315 | G/A | downstream gene variant | — |
| rs146590087 | 6:88,136,248 | A/G | — | uncertain significance |
| rs928254554 | 6:88,136,259 | G/A | — | uncertain significance |
| rs2482702840 | 6:88,138,480 | T/G | — | uncertain significance |
| rs1768102847 | 6:88,138,515 | G/T | — | uncertain significance |
| rs750143246 | 6:88,140,799 | C/A | — | uncertain significance |
| rs781732069 | 6:88,140,823 | A/G | — | uncertain significance |
| rs370548592 | 6:88,140,840 | C/T | — | uncertain significance |
| rs776536200 | 6:88,144,595 | A/G | — | uncertain significance |
| rs375860563 | 6:88,144,637 | G/T | — | uncertain significance |
| rs137999833 | 6:88,144,670 | C/T | — | uncertain significance |
| rs756652919 | 6:88,144,695 | A/G | — | uncertain significance |
| rs6914299 | 6:88,149,176 | T/G | downstream gene variant | — |
| rs1469938390 | 6:88,170,754 | C/A | — | uncertain significance |
| rs760258437 | 6:88,170,764 | A/T | — | uncertain significance |
| rs750748171 | 6:88,170,804 | A/G | — | uncertain significance |
| rs552455955 | 6:88,170,825 | C/T | — | uncertain significance |
| rs139574881 | 6:88,173,748 | G/T | — | uncertain significance |
| rs146571078 | 6:88,173,900 | C/T | — | uncertain significance |
| rs201973315 | 6:88,173,960 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.