CEP128
centrosomal protein 128
Summary
Involved in protein localization. Located in Golgi apparatus; microtubule cytoskeleton; and nuclear membrane. Part of centriolar subdistal appendage. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants84 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1468532778 | 14:80,963,826 | C/T | — | uncertain significance |
| rs570304047 | 14:80,963,832 | T/C | — | uncertain significance |
| rs2503261365 | 14:80,963,849 | T/A | — | uncertain significance |
| rs144263413 | 14:80,963,884 | T/G | — | uncertain significance |
| rs148747041 | 14:80,963,894 | T/G | — | benign |
| rs1887546330 | 14:80,963,917 | T/C | — | uncertain significance |
| rs373014765 | 14:80,971,291 | G/A | — | uncertain significance |
| rs377362585 | 14:80,971,326 | C/T | — | uncertain significance |
| rs1468209981 | 14:80,971,362 | C/T | — | likely benign |
| rs780416924 | 14:80,993,234 | C/A | — | uncertain significance |
| rs773418804 | 14:80,993,239 | T/C | — | uncertain significance |
| rs1888994925 | 14:80,993,242 | C/T | — | uncertain significance |
| rs375253952 | 14:80,993,331 | A/G | — | likely benign |
| rs146120887 | 14:80,997,160 | T/G | — | uncertain significance |
| rs1361016514 | 14:80,997,230 | T/C | — | uncertain significance |
| rs554085697 | 14:81,021,942 | G/A | — | — |
| rs780246010 | 14:81,025,642 | C/T | — | uncertain significance |
| rs145556324 | 14:81,029,261 | G/A | intron variant | — |
| rs762657593 | 14:81,046,755 | T/C | — | uncertain significance |
| rs141751376 | 14:81,107,361 | T/C | intron variant | — |
| rs761119738 | 14:81,209,441 | A/T | — | likely benign |
| rs376263744 | 14:81,209,466 | A/G | — | uncertain significance |
| rs1898918703 | 14:81,209,484 | T/C | — | uncertain significance |
| rs149065030 | 14:81,209,556 | T/C | — | likely benign |
| rs1898925655 | 14:81,209,583 | A/G | — | uncertain significance |
| rs1340029638 | 14:81,223,262 | G/A | — | uncertain significance |
| rs1289843828 | 14:81,223,294 | A/G | — | uncertain significance |
| rs750008544 | 14:81,227,818 | C/A | — | uncertain significance |
| rs1433858836 | 14:81,244,243 | C/T | — | uncertain significance |
| rs375718150 | 14:81,244,335 | T/A | — | uncertain significance |
| rs767533048 | 14:81,244,347 | C/T | — | uncertain significance |
| rs138204688 | 14:81,244,350 | C/T | — | uncertain significance |
| rs149384868 | 14:81,251,312 | T/C | — | uncertain significance |
| rs144670267 | 14:81,251,406 | T/G | — | uncertain significance |
| rs1476447848 | 14:81,251,576 | T/C | — | uncertain significance |
| rs910954614 | 14:81,251,623 | T/G | — | uncertain significance |
| rs142389077 | 14:81,251,633 | T/A | — | uncertain significance |
| rs199526020 | 14:81,251,729 | T/G | — | uncertain significance |
| rs1901352210 | 14:81,251,740 | A/C | — | uncertain significance |
| rs115536488 | 14:81,251,748 | G/C | — | uncertain significance |
| rs1901358621 | 14:81,251,840 | T/C | — | uncertain significance |
| rs749181123 | 14:81,251,846 | G/A | — | uncertain significance |
| rs768640379 | 14:81,251,847 | C/T | — | uncertain significance |
| rs761386038 | 14:81,251,855 | A/G | — | uncertain significance |
| rs753223975 | 14:81,259,156 | G/A | — | uncertain significance |
| rs375266825 | 14:81,259,192 | C/T | — | uncertain significance |
| rs770144174 | 14:81,259,265 | G/T | — | uncertain significance |
| rs367862042 | 14:81,259,286 | G/A | — | uncertain significance |
| rs143121270 | 14:81,259,292 | C/T | — | uncertain significance |
| rs45488095 | 14:81,259,336 | C/T | — | likely benign |
| rs201149406 | 14:81,259,346 | C/T | — | uncertain significance |
| rs145742045 | 14:81,259,354 | C/T | — | likely benign |
| rs566004102 | 14:81,259,436 | C/G | — | uncertain significance |
| rs162171 | 14:81,260,377 | A/T | — | — |
| rs114538296 | 14:81,262,792 | A/C | intron variant | — |
| rs147219747 | 14:81,295,663 | A/G | intron variant | — |
| rs1209084679 | 14:81,297,501 | C/T | — | uncertain significance |
| rs1194936783 | 14:81,297,531 | C/G | — | uncertain significance |
| rs185240818 | 14:81,297,584 | T/C | — | uncertain significance |
| rs2548341645 | 14:81,297,611 | T/C | — | uncertain significance |
| rs199544885 | 14:81,297,630 | G/A | — | uncertain significance |
| rs116610923 | 14:81,297,635 | A/G | — | benign |
| rs371275568 | 14:81,297,636 | C/A | — | uncertain significance |
| rs1674557 | 14:81,302,655 | C/T | — | benign |
| rs749206725 | 14:81,302,656 | G/A | — | likely benign |
| rs150023941 | 14:81,304,567 | C/T | — | uncertain significance |
| rs148571416 | 14:81,307,085 | C/T | — | uncertain significance |
| rs115137924 | 14:81,329,105 | T/G | — | uncertain significance |
| rs1887580707 | 14:81,329,157 | C/G | — | uncertain significance |
| rs139577654 | 14:81,329,169 | G/A | — | uncertain significance |
| rs370474015 | 14:81,329,207 | C/T | — | uncertain significance |
| rs1889315460 | 14:81,362,066 | T/C | — | uncertain significance |
| rs1412444470 | 14:81,362,085 | T/C | — | uncertain significance |
| rs1043286508 | 14:81,366,339 | C/T | — | uncertain significance |
| rs771163272 | 14:81,371,194 | C/T | — | uncertain significance |
| rs376002974 | 14:81,371,233 | C/T | — | uncertain significance |
| rs1282377524 | 14:81,371,266 | T/C | — | likely benign |
| rs996176892 | 14:81,371,267 | G/C | — | uncertain significance |
| rs201719117 | 14:81,380,709 | C/T | — | likely benign |
| rs141572655 | 14:81,382,818 | G/A | — | uncertain significance |
| rs772452675 | 14:81,382,858 | G/A | — | uncertain significance |
| rs188633885 | 14:81,384,981 | C/T | — | — |
| rs12587252 | 14:81,405,922 | C/T | intron variant | — |
| rs17111237 | 14:81,406,341 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.