CEP68
centrosomal protein 68
Summary
Enables protein domain specific binding activity and protein kinase binding activity. Involved in centriole-centriole cohesion and protein localization to organelle. Located in several cellular components, including cytosol; microtubule organizing center; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants86 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6728523 | 2:65,282,708 | G/C | regulatory region variant | — |
| rs74181299 | 2:65,283,972 | T/C | regulatory region variant | — |
| rs2540948 | 2:65,284,623 | T/C | regulatory region variant | — |
| rs2540945 | 2:65,289,825 | A/G | intron variant | — |
| rs2723083 | 2:65,289,949 | C/T | regulatory region variant | — |
| rs768820202 | 2:65,296,588 | G/T | — | uncertain significance |
| rs200538109 | 2:65,296,616 | C/G | — | uncertain significance |
| rs1384775751 | 2:65,296,634 | A/T | — | uncertain significance |
| rs972966595 | 2:65,296,637 | C/T | — | uncertain significance |
| rs199743446 | 2:65,296,700 | A/G | — | uncertain significance |
| rs774012835 | 2:65,296,708 | C/T | — | uncertain significance |
| rs761493048 | 2:65,296,709 | G/T | — | uncertain significance |
| rs1676359486 | 2:65,296,732 | A/G | — | uncertain significance |
| rs766769339 | 2:65,296,735 | T/G | — | uncertain significance |
| rs7572857 | 2:65,296,798 | G/A | missense variant | — |
| rs778115651 | 2:65,296,802 | C/T | — | likely benign |
| rs201901465 | 2:65,296,843 | G/A | — | uncertain significance |
| rs1170749302 | 2:65,296,877 | G/C | — | uncertain significance |
| rs2528209351 | 2:65,296,880 | G/T | — | uncertain significance |
| rs2528209522 | 2:65,296,922 | C/A | — | uncertain significance |
| rs528296468 | 2:65,296,924 | G/A | — | uncertain significance |
| rs373247485 | 2:65,298,595 | A/C | — | uncertain significance |
| rs115640149 | 2:65,298,615 | G/A | — | uncertain significance |
| rs140550134 | 2:65,298,748 | C/T | — | uncertain significance |
| rs1477029762 | 2:65,298,820 | G/A | — | uncertain significance |
| rs1306635041 | 2:65,298,826 | C/T | — | uncertain significance |
| rs369652529 | 2:65,298,832 | C/G | — | uncertain significance |
| rs759074875 | 2:65,298,871 | C/T | — | uncertain significance |
| rs183284304 | 2:65,298,880 | G/A | — | benign |
| rs150735181 | 2:65,298,923 | C/T | — | likely benign |
| rs143870852 | 2:65,299,020 | A/G | — | uncertain significance |
| rs750998759 | 2:65,299,075 | T/C | — | uncertain significance |
| rs780974829 | 2:65,299,095 | C/G | — | uncertain significance |
| rs2528216464 | 2:65,299,117 | A/G | — | uncertain significance |
| rs762071289 | 2:65,299,152 | C/G | — | uncertain significance |
| rs753017494 | 2:65,299,184 | C/A | — | likely benign |
| rs200251289 | 2:65,299,186 | T/C | — | uncertain significance |
| rs780971112 | 2:65,299,188 | G/A | — | uncertain significance |
| rs374258693 | 2:65,299,192 | G/A | — | uncertain significance |
| rs201157959 | 2:65,299,194 | C/T | — | uncertain significance |
| rs200718631 | 2:65,299,204 | C/T | — | uncertain significance |
| rs754877793 | 2:65,299,299 | T/C | — | uncertain significance |
| rs141499084 | 2:65,299,330 | T/A | — | benign |
| rs774988713 | 2:65,299,365 | C/A | — | uncertain significance |
| rs757916444 | 2:65,299,432 | C/T | — | uncertain significance |
| rs192553294 | 2:65,299,452 | G/A | — | uncertain significance |
| rs147566910 | 2:65,299,460 | T/C | — | likely benign |
| rs141435576 | 2:65,299,467 | C/T | — | uncertain significance |
| rs1454196065 | 2:65,299,468 | G/A | — | uncertain significance |
| rs577037216 | 2:65,299,500 | C/T | — | likely benign |
| rs971023170 | 2:65,299,501 | G/A | — | uncertain significance |
| rs780480482 | 2:65,299,534 | C/G | — | uncertain significance |
| rs749690692 | 2:65,299,536 | C/T | — | uncertain significance |
| rs150680996 | 2:65,299,552 | G/A | — | likely benign |
| rs149863693 | 2:65,299,571 | G/A | — | benign |
| rs150135845 | 2:65,299,648 | A/T | — | uncertain significance |
| rs1558563225 | 2:65,299,651 | A/G | — | uncertain significance |
| rs571191573 | 2:65,299,689 | G/C | — | uncertain significance |
| rs1306869342 | 2:65,299,737 | T/A | — | uncertain significance |
| rs1558563440 | 2:65,299,772 | A/C | — | uncertain significance |
| rs202182197 | 2:65,299,802 | T/G | — | uncertain significance |
| rs759272372 | 2:65,299,818 | T/C | — | likely benign |
| rs886342184 | 2:65,299,849 | C/G | — | uncertain significance |
| rs374313300 | 2:65,299,890 | C/A | — | uncertain significance |
| rs188040350 | 2:65,299,928 | C/T | — | likely benign |
| rs146568738 | 2:65,299,964 | G/A | — | benign |
| rs374865357 | 2:65,299,971 | G/A | — | uncertain significance |
| rs375337582 | 2:65,299,972 | G/T | — | uncertain significance |
| rs766572390 | 2:65,299,978 | C/T | — | uncertain significance |
| rs141305652 | 2:65,299,988 | G/A | — | benign |
| rs745370664 | 2:65,300,004 | T/G | — | uncertain significance |
| rs527765164 | 2:65,300,025 | C/T | — | uncertain significance |
| rs373017080 | 2:65,300,026 | G/A | — | uncertain significance |
| rs901797365 | 2:65,300,035 | T/G | — | uncertain significance |
| rs114749990 | 2:65,300,050 | T/C | — | benign |
| rs369444905 | 2:65,300,052 | G/A | — | uncertain significance |
| rs201912409 | 2:65,300,135 | G/A | — | likely benign |
| rs753879555 | 2:65,301,456 | A/G | — | uncertain significance |
| rs137938370 | 2:65,301,501 | A/G | — | likely benign |
| rs79568756 | 2:65,301,547 | C/G | — | benign |
| rs2528233651 | 2:65,305,091 | C/G | — | uncertain significance |
| rs2528244775 | 2:65,309,706 | C/G | — | uncertain significance |
| rs746501565 | 2:65,309,726 | G/A | — | uncertain significance |
| rs769356766 | 2:65,309,733 | G/A | — | likely benign |
| rs767543442 | 2:65,309,753 | G/A | — | uncertain significance |
| rs560205369 | 2:65,309,810 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.