CFAP91
cilia and flagella associated protein 91
Summary
Involved in axonemal central apparatus assembly and spermatogenesis. Predicted to be located in motile cilium and radial spoke stalk. Implicated in spermatogenic failure 51. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants70 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs766267895 | 3:119,421,967 | G/C | — | likely benign |
| rs748598993 | 3:119,422,010 | G/A | — | uncertain significance |
| rs746646225 | 3:119,422,016 | G/A | — | likely benign |
| rs138727483 | 3:119,422,033 | C/T | — | uncertain significance |
| rs138878198 | 3:119,422,043 | C/T | — | uncertain significance |
| rs149348782 | 3:119,422,069 | G/C | — | uncertain significance |
| rs368173878 | 3:119,425,690 | T/C | — | likely benign |
| rs765347077 | 3:119,425,692 | C/T | — | uncertain significance |
| rs775501142 | 3:119,425,721 | C/T | — | uncertain significance |
| rs1182876976 | 3:119,426,294 | A/G | — | uncertain significance |
| rs377264588 | 3:119,426,353 | C/T | — | uncertain significance |
| rs1489471988 | 3:119,426,368 | C/T | — | uncertain significance |
| rs760911940 | 3:119,426,396 | G/A | — | likely benign |
| rs1310762739 | 3:119,427,443 | A/C | — | uncertain significance |
| rs1425298704 | 3:119,427,497 | A/G | — | likely benign |
| rs1205193979 | 3:119,427,503 | G/C | — | uncertain significance |
| rs758418675 | 3:119,427,505 | T/C | — | uncertain significance |
| rs1397488258 | 3:119,427,508 | A/G | — | uncertain significance |
| rs927479670 | 3:119,428,688 | C/T | — | uncertain significance |
| rs200247170 | 3:119,428,735 | G/A | — | likely benign |
| rs201703483 | 3:119,434,406 | T/C | — | uncertain significance |
| rs951168502 | 3:119,434,420 | A/T | — | uncertain significance |
| rs936985209 | 3:119,434,443 | A/G | — | uncertain significance |
| rs147597066 | 3:119,434,591 | G/A | — | pathogenic |
| rs34845376 | 3:119,436,009 | G/T | regulatory region variant | — |
| rs771332145 | 3:119,445,023 | G/A | — | uncertain significance |
| rs759496105 | 3:119,445,029 | C/G | — | uncertain significance |
| rs562410253 | 3:119,445,071 | G/A | — | uncertain significance |
| rs2053781227 | 3:119,445,081 | C/A | — | uncertain significance |
| rs2545598011 | 3:119,445,187 | G/C | — | uncertain significance |
| rs201238294 | 3:119,449,081 | G/T | — | uncertain significance |
| rs758399473 | 3:119,449,113 | C/T | — | uncertain significance |
| rs146078151 | 3:119,449,114 | G/A | — | uncertain significance |
| rs755035891 | 3:119,449,140 | A/G | — | uncertain significance |
| rs374317339 | 3:119,449,158 | C/T | — | uncertain significance |
| rs1325493314 | 3:119,449,202 | A/C | — | uncertain significance |
| rs148476947 | 3:119,449,209 | C/T | — | uncertain significance |
| rs201377329 | 3:119,451,192 | G/A | — | uncertain significance |
| rs762465669 | 3:119,451,243 | C/T | — | uncertain significance |
| rs538656317 | 3:119,451,275 | A/T | — | uncertain significance |
| rs556925393 | 3:119,451,276 | A/C | — | uncertain significance |
| rs772507244 | 3:119,451,287 | T/C | — | uncertain significance |
| rs765649223 | 3:119,452,256 | C/A | — | uncertain significance |
| rs149820036 | 3:119,452,345 | G/A | — | uncertain significance |
| rs780817834 | 3:119,456,214 | C/T | — | uncertain significance |
| rs1453761770 | 3:119,456,229 | A/C | — | uncertain significance |
| rs374970805 | 3:119,456,255 | C/A | — | uncertain significance |
| rs199600362 | 3:119,456,261 | C/T | — | uncertain significance |
| rs367681304 | 3:119,456,282 | A/G | — | likely benign |
| rs371677982 | 3:119,456,294 | C/T | — | uncertain significance |
| rs1057354410 | 3:119,456,328 | A/G | — | uncertain significance |
| rs764922877 | 3:119,458,111 | G/C | — | uncertain significance |
| rs752490129 | 3:119,458,114 | A/C | — | uncertain significance |
| rs763924717 | 3:119,459,441 | C/T | — | uncertain significance |
| rs1412218297 | 3:119,459,465 | G/C | — | uncertain significance |
| rs757703206 | 3:119,459,495 | C/T | — | likely pathogenic |
| rs772352151 | 3:119,459,513 | C/G | — | uncertain significance |
| rs1291488644 | 3:119,462,933 | G/T | — | uncertain significance |
| rs201045322 | 3:119,462,955 | G/A | — | uncertain significance |
| rs1178010279 | 3:119,462,988 | G/A | — | uncertain significance |
| rs141246031 | 3:119,462,991 | G/A | — | uncertain significance |
| rs200730852 | 3:119,463,011 | C/T | — | uncertain significance |
| rs994345392 | 3:119,466,009 | A/G | — | uncertain significance |
| rs199566013 | 3:119,466,022 | G/A | — | uncertain significance |
| rs200409004 | 3:119,466,660 | G/A | — | uncertain significance |
| rs148036142 | 3:119,466,683 | A/G | — | uncertain significance |
| rs896679701 | 3:119,469,792 | G/A | — | uncertain significance |
| rs776934715 | 3:119,469,847 | G/A | — | uncertain significance |
| rs201952221 | 3:119,469,889 | C/T | — | likely benign |
| rs2545622375 | 3:119,469,932 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.