CEP97
centrosomal protein 97
Summary
Predicted to enable U2 snRNA binding activity and calmodulin binding activity. Involved in negative regulation of cilium assembly and regulation of mitotic spindle assembly. Located in centriole and centrosome. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants196 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201771736 | 3:101,443,534 | G/T | — | conflicting classifications of pathogenicity |
| rs373337025 | 3:101,443,548 | T/C | — | likely benign |
| rs769100893 | 3:101,443,570 | C/G | — | likely benign |
| rs368851013 | 3:101,443,580 | C/T | — | likely benign |
| rs112981951 | 3:101,445,425 | G/A | — | benign |
| rs1576673546 | 3:101,445,449 | A/C | — | uncertain significance |
| rs1359269119 | 3:101,445,469 | A/G | — | likely benign |
| rs188412281 | 3:101,445,482 | C/A | — | uncertain significance |
| rs201833020 | 3:101,445,511 | C/G | — | uncertain significance |
| rs111912421 | 3:101,445,570 | G/A | — | benign |
| rs759026391 | 3:101,445,583 | A/T | — | uncertain significance |
| rs776962234 | 3:101,446,222 | T/C | — | likely benign |
| rs757656908 | 3:101,446,225 | A/T | — | uncertain significance |
| rs1937927675 | 3:101,446,227 | T/C | — | uncertain significance |
| rs139328680 | 3:101,446,245 | C/T | — | uncertain significance |
| rs547567941 | 3:101,446,254 | C/T | — | uncertain significance |
| rs143663483 | 3:101,446,270 | C/T | — | uncertain significance |
| rs1024966245 | 3:101,446,279 | C/T | — | uncertain significance |
| rs548722311 | 3:101,446,280 | G/A | — | likely benign |
| rs536511998 | 3:101,446,289 | T/C | — | likely benign |
| rs1417174177 | 3:101,446,303 | C/T | — | uncertain significance |
| rs191543705 | 3:101,446,305 | C/T | — | uncertain significance |
| rs2545819523 | 3:101,446,317 | G/A | — | uncertain significance |
| rs1256764915 | 3:101,446,347 | C/T | — | uncertain significance |
| rs145437722 | 3:101,446,350 | C/T | — | benign |
| rs1254648284 | 3:101,447,702 | G/A | — | uncertain significance |
| rs141892594 | 3:101,447,721 | C/T | — | likely benign |
| rs890669638 | 3:101,447,790 | G/T | — | likely benign |
| rs2545820729 | 3:101,447,793 | T/C | — | likely benign |
| rs760163007 | 3:101,450,707 | C/T | — | uncertain significance |
| rs201836749 | 3:101,450,717 | C/T | — | uncertain significance |
| rs1448470191 | 3:101,450,747 | A/G | — | uncertain significance |
| rs767646219 | 3:101,450,756 | A/G | — | uncertain significance |
| rs948864139 | 3:101,450,761 | T/G | — | likely benign |
| rs1327916528 | 3:101,450,766 | T/A | — | uncertain significance |
| rs914451601 | 3:101,450,768 | G/A | — | uncertain significance |
| rs139940133 | 3:101,450,770 | A/C | — | likely benign |
| rs2545823375 | 3:101,450,786 | G/A | — | uncertain significance |
| rs776072662 | 3:101,450,810 | G/T | — | likely benign |
| rs1441946316 | 3:101,451,372 | C/T | — | uncertain significance |
| rs368081844 | 3:101,451,373 | G/C | — | likely benign |
| rs901516896 | 3:101,451,411 | T/C | — | uncertain significance |
| rs200003550 | 3:101,451,426 | A/G | — | uncertain significance |
| rs146280894 | 3:101,451,430 | G/A | — | likely benign |
| rs139210877 | 3:101,451,433 | G/T | — | likely benign |
| rs193228690 | 3:101,451,439 | C/T | — | likely benign |
| rs144895544 | 3:101,451,460 | C/G | — | benign |
| rs201166758 | 3:101,451,483 | T/C | — | likely benign |
| rs2545824039 | 3:101,451,515 | T/C | — | likely benign |
| rs763999925 | 3:101,474,263 | C/A | — | likely benign |
| rs779653506 | 3:101,474,320 | C/T | — | uncertain significance |
| rs144348649 | 3:101,474,321 | G/A | — | uncertain significance |
| rs755565702 | 3:101,474,322 | G/A | — | likely benign |
| rs199841045 | 3:101,474,325 | T/A | — | likely benign |
| rs1032775606 | 3:101,474,332 | C/A | — | uncertain significance |
| rs2545843447 | 3:101,474,344 | G/T | — | uncertain significance |
| rs1938979472 | 3:101,474,354 | T/C | — | uncertain significance |
| rs567184992 | 3:101,474,356 | G/A | — | likely benign |
| rs776825736 | 3:101,474,374 | A/T | — | uncertain significance |
| rs761683619 | 3:101,474,384 | T/C | — | uncertain significance |
| rs2926543 | 3:101,474,385 | A/T | — | likely benign |
| rs145761247 | 3:101,474,398 | G/A | — | likely benign |
| rs151291975 | 3:101,474,429 | G/A | — | uncertain significance |
| rs370056936 | 3:101,474,445 | C/T | — | likely benign |
| rs1939024810 | 3:101,475,890 | G/A | — | likely benign |
| rs1939025462 | 3:101,475,911 | C/T | — | uncertain significance |
| rs766127476 | 3:101,475,922 | G/A | — | likely benign |
| rs1255933692 | 3:101,475,928 | G/A | — | uncertain significance |
| rs1939026709 | 3:101,475,937 | C/A | — | uncertain significance |
| rs2545844899 | 3:101,475,950 | T/C | — | likely benign |
| rs59720918 | 3:101,475,968 | G/C | — | benign |
| rs781563241 | 3:101,475,977 | A/G | — | uncertain significance |
| rs2545845003 | 3:101,476,019 | T/C | — | uncertain significance |
| rs1170441231 | 3:101,476,023 | A/C | — | uncertain significance |
| rs1388953804 | 3:101,476,465 | T/C | — | uncertain significance |
| rs150469920 | 3:101,476,481 | C/T | — | uncertain significance |
| rs753993583 | 3:101,476,483 | G/A | — | uncertain significance |
| rs755022116 | 3:101,476,516 | A/T | — | uncertain significance |
| rs778998982 | 3:101,476,523 | A/C | — | uncertain significance |
| rs746948564 | 3:101,476,529 | A/G | — | uncertain significance |
| rs767173679 | 3:101,476,538 | C/T | — | uncertain significance |
| rs141860565 | 3:101,476,539 | G/A | — | benign |
| rs2545845529 | 3:101,476,544 | A/G | — | uncertain significance |
| rs1174945578 | 3:101,476,561 | T/C | — | uncertain significance |
| rs1386153102 | 3:101,476,569 | C/T | — | likely benign |
| rs773873294 | 3:101,476,574 | C/T | — | uncertain significance |
| rs1060499739 | 3:101,476,598 | A/G | missense variant | pathogenic |
| rs145072852 | 3:101,476,645 | C/T | — | likely benign |
| rs532372200 | 3:101,476,647 | C/T | — | likely benign |
| rs2545845694 | 3:101,476,651 | T/G | — | uncertain significance |
| rs117590742 | 3:101,476,656 | G/A | — | likely benign |
| rs138854860 | 3:101,476,672 | G/T | — | likely benign |
| rs374370393 | 3:101,476,699 | C/T | — | uncertain significance |
| rs1244137632 | 3:101,476,724 | G/T | — | uncertain significance |
| rs77015203 | 3:101,476,732 | T/G | — | conflicting classifications of pathogenicity |
| rs146247413 | 3:101,476,758 | A/G | — | benign |
| rs368952768 | 3:101,476,760 | A/T | — | uncertain significance |
| rs778631146 | 3:101,476,764 | A/C | — | uncertain significance |
| rs2545845994 | 3:101,476,789 | G/A | — | uncertain significance |
| rs771592287 | 3:101,476,799 | A/T | — | uncertain significance |
Showing 100 of 196 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.