CEP95
centrosomal protein 95
Summary
Located in centrosome and spindle pole. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1555673172 | 17:62,503,219 | G/A | — | uncertain significance |
| rs369515401 | 17:62,504,721 | A/G | — | likely benign |
| rs200913762 | 17:62,504,749 | A/G | — | uncertain significance |
| rs576870712 | 17:62,504,751 | A/G | — | uncertain significance |
| rs782464005 | 17:62,504,753 | A/G | — | uncertain significance |
| rs782105906 | 17:62,504,808 | T/A | — | uncertain significance |
| rs782711597 | 17:62,504,817 | A/G | — | uncertain significance |
| rs57166100 | 17:62,506,280 | T/C | upstream gene variant | — |
| rs2509625254 | 17:62,506,348 | T/C | — | uncertain significance |
| rs200297929 | 17:62,506,376 | G/T | — | uncertain significance |
| rs376238247 | 17:62,512,874 | G/A | — | uncertain significance |
| rs782337349 | 17:62,515,525 | C/T | — | uncertain significance |
| rs181848970 | 17:62,515,551 | A/G | — | uncertain significance |
| rs186393767 | 17:62,516,930 | C/G | intron variant | — |
| rs148050755 | 17:62,516,959 | A/C | intron variant | — |
| rs200923114 | 17:62,517,603 | C/T | — | uncertain significance |
| rs531625047 | 17:62,518,861 | C/G | — | uncertain significance |
| rs781792125 | 17:62,518,885 | A/G | — | uncertain significance |
| rs368152443 | 17:62,518,938 | A/G | — | uncertain significance |
| rs374645585 | 17:62,519,000 | C/T | — | likely benign |
| rs75262331 | 17:62,521,763 | A/G | intron variant | — |
| rs2509689979 | 17:62,521,937 | A/C | — | uncertain significance |
| rs781934920 | 17:62,521,951 | C/G | — | uncertain significance |
| rs1289374503 | 17:62,521,958 | A/G | — | uncertain significance |
| rs2509691660 | 17:62,522,239 | G/A | — | uncertain significance |
| rs367639602 | 17:62,523,253 | C/T | — | uncertain significance |
| rs781914989 | 17:62,523,275 | A/G | — | uncertain significance |
| rs2509695599 | 17:62,523,305 | T/C | — | uncertain significance |
| rs374558949 | 17:62,523,317 | C/G | — | uncertain significance |
| rs781868398 | 17:62,523,352 | G/A | — | likely benign |
| rs377023210 | 17:62,525,411 | T/C | — | uncertain significance |
| rs782543732 | 17:62,525,414 | A/G | — | likely benign |
| rs1555679799 | 17:62,525,493 | G/A | — | uncertain significance |
| rs2509704996 | 17:62,525,514 | G/C | — | uncertain significance |
| rs781841347 | 17:62,525,529 | G/A | — | likely benign |
| rs1353494003 | 17:62,527,118 | T/A | — | uncertain significance |
| rs1968309025 | 17:62,528,024 | G/A | — | uncertain significance |
| rs1031227435 | 17:62,528,119 | A/G | — | uncertain significance |
| rs782531825 | 17:62,529,064 | G/T | — | uncertain significance |
| rs782043221 | 17:62,529,085 | G/A | — | uncertain significance |
| rs781888057 | 17:62,530,803 | A/G | — | uncertain significance |
| rs117353725 | 17:62,530,906 | C/A | upstream gene variant | — |
| rs373296848 | 17:62,533,220 | C/A | — | uncertain significance |
| rs782819510 | 17:62,533,811 | G/A | — | uncertain significance |
| rs575666923 | 17:62,533,821 | G/A | — | uncertain significance |
| rs781839865 | 17:62,533,835 | G/A | — | uncertain significance |
| rs782779989 | 17:62,533,838 | C/T | — | uncertain significance |
| rs200397675 | 17:62,533,872 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.