CEP85L
centrosomal protein 85L
Summary
The protein encoded by this gene was identified as a breast cancer antigen. Nothing more is known of its function at this time. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
Known Variants94 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1772441410 | 6:118,786,605 | T/C | — | uncertain significance |
| rs181970377 | 6:118,786,639 | T/C | — | likely benign |
| rs11752626 | 6:118,788,652 | G/T | intron variant | — |
| rs17825652 | 6:118,788,986 | G/A | intron variant | — |
| rs2533740355 | 6:118,790,354 | A/G | — | uncertain significance |
| rs2533741192 | 6:118,790,400 | G/A | — | likely pathogenic |
| rs2533753671 | 6:118,791,728 | A/G | — | uncertain significance |
| rs774834119 | 6:118,791,761 | A/G | — | uncertain significance |
| rs761163642 | 6:118,801,033 | C/A | — | uncertain significance |
| rs2533821875 | 6:118,801,071 | T/C | — | uncertain significance |
| rs746240342 | 6:118,802,979 | T/C | — | uncertain significance |
| rs548222922 | 6:118,803,007 | T/C | — | likely benign |
| rs774638980 | 6:118,803,026 | T/G | — | uncertain significance |
| rs1340109090 | 6:118,803,087 | G/C | — | uncertain significance |
| rs1401607093 | 6:118,804,866 | T/A | — | uncertain significance |
| rs1459879319 | 6:118,804,891 | T/C | — | uncertain significance |
| rs2533856224 | 6:118,804,970 | C/A | — | uncertain significance |
| rs25422 | 6:118,807,847 | C/T | intron variant | — |
| rs9481816 | 6:118,812,403 | T/C | intron variant | — |
| rs1166816000 | 6:118,812,865 | T/C | — | uncertain significance |
| rs2533916236 | 6:118,812,891 | T/C | — | likely benign |
| rs148635510 | 6:118,812,980 | C/T | — | likely benign |
| rs2533917788 | 6:118,813,024 | T/G | — | uncertain significance |
| rs377688242 | 6:118,832,525 | C/T | — | uncertain significance |
| rs138089888 | 6:118,832,526 | G/A | — | likely benign |
| rs757345109 | 6:118,832,555 | A/T | — | uncertain significance |
| rs1017418937 | 6:118,844,969 | C/T | — | uncertain significance |
| rs777321707 | 6:118,844,989 | C/T | — | uncertain significance |
| rs2534124737 | 6:118,845,001 | T/C | — | uncertain significance |
| rs2534125288 | 6:118,845,057 | A/C | — | uncertain significance |
| rs533727346 | 6:118,845,065 | G/A | — | uncertain significance |
| rs185846037 | 6:118,869,224 | C/T | — | likely benign |
| rs756289789 | 6:118,886,697 | T/C | — | likely benign |
| rs1213659225 | 6:118,886,714 | T/G | — | uncertain significance |
| rs548729674 | 6:118,886,717 | C/T | — | likely benign |
| rs2534370024 | 6:118,886,728 | A/T | — | likely benign |
| rs2534370435 | 6:118,886,769 | C/G | — | uncertain significance |
| rs781502949 | 6:118,886,771 | G/T | — | uncertain significance |
| rs2534370920 | 6:118,886,817 | A/G | — | uncertain significance |
| rs140573157 | 6:118,886,832 | C/T | — | uncertain significance |
| rs145696727 | 6:118,886,833 | G/A | — | likely benign |
| rs1432157169 | 6:118,886,856 | C/G | — | uncertain significance |
| rs751661999 | 6:118,886,874 | G/C | — | uncertain significance |
| rs538687244 | 6:118,886,875 | C/T | — | likely benign |
| rs749577914 | 6:118,886,919 | T/C | — | uncertain significance |
| rs760585658 | 6:118,886,928 | T/C | — | uncertain significance |
| rs761548752 | 6:118,886,943 | T/C | — | uncertain significance |
| rs3734382 | 6:118,886,961 | G/T | — | benign |
| rs779389767 | 6:118,886,989 | T/G | — | uncertain significance |
| rs143565368 | 6:118,887,023 | T/C | — | uncertain significance |
| rs2534373045 | 6:118,887,042 | A/G | — | uncertain significance |
| rs148059317 | 6:118,887,053 | T/G | — | likely benign |
| rs371462128 | 6:118,887,058 | T/C | — | uncertain significance |
| rs1186267115 | 6:118,887,098 | T/C | — | uncertain significance |
| rs769720109 | 6:118,887,156 | T/C | — | uncertain significance |
| rs747593968 | 6:118,887,220 | G/T | — | likely benign |
| rs1779485563 | 6:118,887,257 | G/T | — | uncertain significance |
| rs141322226 | 6:118,887,260 | C/T | — | uncertain significance |
| rs2114998574 | 6:118,887,270 | T/C | — | uncertain significance |
| rs915147792 | 6:118,887,287 | T/A | — | uncertain significance |
| rs3734381 | 6:118,887,303 | T/C | — | benign |
| rs201125021 | 6:118,887,335 | C/G | — | uncertain significance |
| rs767185741 | 6:118,887,351 | C/A | — | uncertain significance |
| rs200615871 | 6:118,887,387 | C/T | — | likely benign |
| rs2534377297 | 6:118,887,396 | T/C | — | uncertain significance |
| rs751002966 | 6:118,887,464 | C/A | — | uncertain significance |
| rs12197704 | 6:118,899,681 | T/C | — | — |
| rs1774226763 | 6:118,953,611 | C/T | — | pathogenic |
| rs754052089 | 6:118,953,613 | C/A | — | pathogenic |
| rs2115322443 | 6:118,953,614 | A/T | — | pathogenic |
| rs1774227158 | 6:118,953,615 | C/A | — | pathogenic |
| rs373910393 | 6:118,953,622 | C/T | — | uncertain significance |
| rs1774228815 | 6:118,953,643 | C/T | — | likely pathogenic |
| rs1774228957 | 6:118,953,645 | A/G | — | pathogenic |
| rs2533697083 | 6:118,953,651 | G/A | — | uncertain significance |
| rs1774229245 | 6:118,953,655 | C/T | — | likely pathogenic |
| rs2115322620 | 6:118,953,659 | A/C | — | likely pathogenic |
| rs1554234607 | 6:118,953,666 | G/A | — | conflicting classifications of pathogenicity |
| rs2115322699 | 6:118,953,675 | C/T | — | conflicting classifications of pathogenicity |
| rs1774230502 | 6:118,953,676 | T/A | — | likely pathogenic |
| rs1774231777 | 6:118,953,700 | G/A | — | uncertain significance |
| rs529696554 | 6:118,953,717 | G/C | — | uncertain significance |
| rs6906287 | 6:118,962,740 | T/C | intron variant | — |
| rs1330421078 | 6:118,972,366 | G/A | — | uncertain significance |
| rs1050048493 | 6:118,972,399 | C/G | — | uncertain significance |
| rs1392751549 | 6:118,972,405 | C/G | — | uncertain significance |
| rs187158499 | 6:118,972,413 | G/A | — | benign |
| rs1775537467 | 6:118,972,431 | A/G | — | pathogenic |
| rs1775537638 | 6:118,972,432 | T/A | — | likely pathogenic |
| rs2115386642 | 6:118,972,441 | A/G | — | benign |
| rs957031499 | 6:118,973,938 | A/C | — | uncertain significance |
| rs9285430 | 6:118,989,175 | T/C | intron variant | — |
| rs11756438 | 6:118,993,632 | C/A | intron variant | — |
| rs3902035 | 6:119,000,232 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.