CEP72
centrosomal protein 72
Summary
The product of this gene is a member of the leucine-rich-repeat (LRR) superfamily of proteins. The protein is localized to the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. [provided by RefSeq, Jul 2008]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375238784 | 5:612,481 | C/G | — | uncertain significance |
| rs1389615006 | 5:612,483 | C/G | — | uncertain significance |
| rs774263225 | 5:612,492 | C/T | — | uncertain significance |
| rs2477998627 | 5:612,526 | C/G | — | uncertain significance |
| rs1161899627 | 5:612,556 | T/C | — | uncertain significance |
| rs7726839 | 5:618,586 | A/G | intron variant | — |
| rs745962439 | 5:619,111 | T/G | — | uncertain significance |
| rs138365408 | 5:619,210 | G/A | — | uncertain significance |
| rs757627585 | 5:620,230 | A/G | — | uncertain significance |
| rs768607398 | 5:620,259 | C/T | — | uncertain significance |
| rs542279058 | 5:620,335 | G/A | — | uncertain significance |
| rs62001006 | 5:624,587 | C/T | — | benign |
| rs199576925 | 5:624,588 | G/A | — | uncertain significance |
| rs538033713 | 5:624,592 | G/A | — | uncertain significance |
| rs143821999 | 5:624,597 | G/A | — | uncertain significance |
| rs147256778 | 5:624,613 | G/A | — | uncertain significance |
| rs773830505 | 5:624,635 | T/G | — | uncertain significance |
| rs781032681 | 5:624,654 | G/A | — | uncertain significance |
| rs763669484 | 5:633,903 | A/G | — | uncertain significance |
| rs2478224104 | 5:633,925 | A/G | — | uncertain significance |
| rs1343094569 | 5:633,936 | G/A | — | uncertain significance |
| rs776206996 | 5:633,946 | C/T | — | uncertain significance |
| rs371468447 | 5:633,983 | C/G | — | uncertain significance |
| rs760406184 | 5:634,036 | G/A | — | uncertain significance |
| rs201789250 | 5:634,048 | C/G | — | uncertain significance |
| rs756540415 | 5:634,051 | G/A | — | likely benign |
| rs2478239984 | 5:635,517 | T/G | — | uncertain significance |
| rs1737520719 | 5:635,527 | G/T | — | uncertain significance |
| rs199657985 | 5:635,531 | G/C | — | uncertain significance |
| rs900263051 | 5:635,538 | C/A | — | uncertain significance |
| rs754243480 | 5:635,549 | G/A | — | uncertain significance |
| rs867301116 | 5:635,559 | C/T | — | uncertain significance |
| rs369984910 | 5:635,628 | C/T | — | uncertain significance |
| rs765498962 | 5:635,651 | G/A | — | uncertain significance |
| rs200328644 | 5:635,660 | C/T | — | uncertain significance |
| rs143569794 | 5:635,661 | G/C | — | uncertain significance |
| rs199729073 | 5:635,679 | C/T | — | likely benign |
| rs145377725 | 5:637,731 | G/A | — | uncertain significance |
| rs756393827 | 5:637,791 | A/G | — | uncertain significance |
| rs1176786042 | 5:637,806 | C/A | — | uncertain significance |
| rs369797124 | 5:637,838 | G/C | — | uncertain significance |
| rs766190281 | 5:637,887 | C/T | — | likely benign |
| rs201002445 | 5:637,910 | C/T | — | uncertain significance |
| rs760155795 | 5:639,259 | C/T | — | uncertain significance |
| rs200645880 | 5:639,271 | C/T | — | uncertain significance |
| rs2478283365 | 5:639,333 | T/C | — | uncertain significance |
| rs572280484 | 5:640,528 | G/A | — | uncertain significance |
| rs371974342 | 5:640,639 | C/T | — | uncertain significance |
| rs547677013 | 5:640,670 | G/A | — | uncertain significance |
| rs1259174609 | 5:644,517 | C/T | — | uncertain significance |
| rs2478380967 | 5:647,925 | C/G | — | uncertain significance |
| rs149664534 | 5:647,929 | C/G | — | uncertain significance |
| rs762025257 | 5:647,971 | A/G | — | uncertain significance |
| rs62650519 | 5:649,405 | A/C | — | — |
| rs1439809819 | 5:653,117 | C/T | — | uncertain significance |
| rs777894377 | 5:653,170 | G/A | — | uncertain significance |
| rs753253437 | 5:653,215 | A/G | — | uncertain significance |
| rs4957082 | 5:658,160 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.