CFAP58
cilia and flagella associated protein 58
Summary
Involved in protein localization to motile cilium; sperm axoneme assembly; and sperm mitochondrial sheath assembly. Located in sperm midpiece. Implicated in spermatogenic failure 49. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10883994 | 10:106,106,874 | G/T | — | — |
| rs2493125044 | 10:106,118,177 | C/A | — | uncertain significance |
| rs376327025 | 10:106,118,253 | A/G | — | uncertain significance |
| rs139964001 | 10:106,118,310 | A/G | — | uncertain significance |
| rs753501281 | 10:106,118,316 | C/T | — | uncertain significance |
| rs200132388 | 10:106,118,324 | G/A | — | uncertain significance |
| rs1213412539 | 10:106,124,491 | C/T | — | likely benign |
| rs547278811 | 10:106,124,526 | C/G | — | uncertain significance |
| rs376842731 | 10:106,124,579 | G/C | — | uncertain significance |
| rs201046238 | 10:106,125,621 | G/A | — | uncertain significance |
| rs540840290 | 10:106,125,680 | C/A | — | uncertain significance |
| rs2014780475 | 10:106,128,215 | A/G | — | uncertain significance |
| rs1236182598 | 10:106,128,239 | T/G | — | uncertain significance |
| rs2493148347 | 10:106,130,653 | G/A | — | uncertain significance |
| rs762542201 | 10:106,130,692 | G/A | — | uncertain significance |
| rs2014814811 | 10:106,130,696 | A/C | — | uncertain significance |
| rs781690295 | 10:106,136,613 | A/G | — | uncertain significance |
| rs544934450 | 10:106,137,271 | C/T | — | — |
| rs568288972 | 10:106,139,800 | C/T | — | uncertain significance |
| rs144394752 | 10:106,139,806 | A/G | — | likely benign |
| rs759516327 | 10:106,139,808 | G/A | — | uncertain significance |
| rs368633237 | 10:106,139,809 | C/T | — | uncertain significance |
| rs146462239 | 10:106,139,850 | G/A | — | uncertain significance |
| rs754222797 | 10:106,139,876 | C/A | — | likely benign |
| rs199842560 | 10:106,139,938 | G/A | — | uncertain significance |
| rs185000542 | 10:106,139,941 | A/G | — | uncertain significance |
| rs145473772 | 10:106,139,944 | G/A | — | uncertain significance |
| rs200619709 | 10:106,139,971 | C/T | — | uncertain significance |
| rs145302969 | 10:106,139,973 | C/T | — | likely pathogenic |
| rs142218964 | 10:106,152,126 | T/C | — | uncertain significance |
| rs145923348 | 10:106,153,104 | G/A | — | uncertain significance |
| rs749858144 | 10:106,153,123 | A/G | — | uncertain significance |
| rs769307766 | 10:106,153,124 | T/G | — | uncertain significance |
| rs150206828 | 10:106,153,199 | A/T | — | uncertain significance |
| rs201643990 | 10:106,153,201 | C/A | — | uncertain significance |
| rs544826621 | 10:106,159,139 | C/T | — | pathogenic |
| rs768320781 | 10:106,159,217 | G/T | — | uncertain significance |
| rs140319819 | 10:106,159,223 | G/A | — | uncertain significance |
| rs147649081 | 10:106,160,516 | A/C | — | uncertain significance |
| rs759374943 | 10:106,160,527 | G/C | — | uncertain significance |
| rs779819795 | 10:106,160,609 | C/T | — | uncertain significance |
| rs144481663 | 10:106,160,612 | C/T | — | uncertain significance |
| rs1316896208 | 10:106,160,637 | G/A | — | uncertain significance |
| rs749988574 | 10:106,160,664 | A/G | — | uncertain significance |
| rs770244239 | 10:106,163,498 | T/C | — | uncertain significance |
| rs776020889 | 10:106,163,504 | T/C | — | uncertain significance |
| rs2012308449 | 10:106,163,505 | G/T | — | uncertain significance |
| rs141539826 | 10:106,163,519 | T/C | — | uncertain significance |
| rs41291850 | 10:106,163,533 | C/T | — | likely benign |
| rs369701921 | 10:106,163,539 | C/T | — | pathogenic |
| rs761602798 | 10:106,166,501 | C/A | — | uncertain significance |
| rs17117025 | 10:106,188,433 | C/G | intron variant | — |
| rs184289122 | 10:106,191,229 | A/G | intron variant | — |
| rs138922164 | 10:106,192,486 | C/T | intron variant | — |
| rs2013131818 | 10:106,207,473 | C/A | — | pathogenic |
| rs776932226 | 10:106,207,499 | G/A | — | uncertain significance |
| rs1300065314 | 10:106,207,505 | C/A | — | uncertain significance |
| rs751927868 | 10:106,207,527 | G/C | — | uncertain significance |
| rs371540971 | 10:106,207,541 | G/A | — | uncertain significance |
| rs140537135 | 10:106,207,547 | C/T | — | uncertain significance |
| rs957271361 | 10:106,209,941 | A/G | — | uncertain significance |
| rs146139460 | 10:106,214,189 | C/G | — | uncertain significance |
| rs368177180 | 10:106,214,191 | C/G | — | likely benign |
| rs771374424 | 10:106,214,194 | C/G | — | uncertain significance |
| rs149402131 | 10:106,214,204 | T/A | — | likely benign |
| rs74741614 | 10:106,214,272 | C/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.