CNTROB
centrobin, centriole duplication and spindle assembly protein
Summary
This gene encodes a centrosomal protein that interacts with BRCA2, and is required for centriole duplication and cytokinesis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]
Known Variants72 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs749189728 | 17:7,836,434 | G/C | — | likely benign |
| rs757252037 | 17:7,836,435 | G/A | — | uncertain significance |
| rs372506805 | 17:7,836,473 | G/C | — | uncertain significance |
| rs773298811 | 17:7,836,482 | C/A | — | uncertain significance |
| rs774781412 | 17:7,836,489 | C/T | — | uncertain significance |
| rs1567903775 | 17:7,836,501 | C/A | — | uncertain significance |
| rs530707394 | 17:7,836,591 | A/G | — | uncertain significance |
| rs1972737837 | 17:7,836,596 | G/A | — | uncertain significance |
| rs377545407 | 17:7,836,605 | G/A | — | uncertain significance |
| rs148253487 | 17:7,836,611 | G/A | — | uncertain significance |
| rs776882326 | 17:7,837,493 | G/A | — | uncertain significance |
| rs376762379 | 17:7,837,505 | A/T | — | uncertain significance |
| rs147900154 | 17:7,837,819 | G/A | — | uncertain significance |
| rs149438589 | 17:7,837,861 | T/C | — | uncertain significance |
| rs779360762 | 17:7,838,374 | T/C | — | uncertain significance |
| rs201342482 | 17:7,838,408 | C/A | — | uncertain significance |
| rs1037585879 | 17:7,838,673 | A/C | — | — |
| rs2545303573 | 17:7,839,729 | C/A | — | uncertain significance |
| rs142280568 | 17:7,839,761 | C/T | — | likely benign |
| rs139240698 | 17:7,839,778 | C/T | — | likely benign |
| rs781319152 | 17:7,839,782 | G/A | — | uncertain significance |
| rs576711195 | 17:7,840,029 | G/A | — | uncertain significance |
| rs145425422 | 17:7,840,097 | C/T | — | uncertain significance |
| rs36064728 | 17:7,840,492 | G/A | — | uncertain significance |
| rs149069306 | 17:7,840,531 | A/G | — | uncertain significance |
| rs371997214 | 17:7,840,534 | G/A | — | uncertain significance |
| rs377613708 | 17:7,842,879 | C/T | — | uncertain significance |
| rs764942032 | 17:7,842,904 | G/A | — | uncertain significance |
| rs769518030 | 17:7,842,940 | G/A | — | uncertain significance |
| rs201649892 | 17:7,842,958 | G/A | — | likely benign |
| rs138511450 | 17:7,843,027 | C/T | — | uncertain significance |
| rs200520635 | 17:7,843,040 | G/T | — | uncertain significance |
| rs756011585 | 17:7,843,441 | G/A | — | uncertain significance |
| rs748617832 | 17:7,843,486 | C/T | — | uncertain significance |
| rs1370912513 | 17:7,843,516 | C/G | — | uncertain significance |
| rs760076702 | 17:7,846,728 | G/A | — | uncertain significance |
| rs2545356397 | 17:7,846,742 | T/C | — | uncertain significance |
| rs754330618 | 17:7,846,782 | G/A | — | uncertain significance |
| rs761965478 | 17:7,847,469 | C/T | — | uncertain significance |
| rs1315307928 | 17:7,847,471 | C/G | — | uncertain significance |
| rs755363090 | 17:7,847,518 | C/T | — | uncertain significance |
| rs749496408 | 17:7,847,816 | G/A | — | uncertain significance |
| rs776304006 | 17:7,847,858 | C/T | — | uncertain significance |
| rs150125113 | 17:7,847,918 | C/A | — | uncertain significance |
| rs145492026 | 17:7,847,940 | C/T | — | likely benign |
| rs769027244 | 17:7,849,047 | C/T | — | likely benign |
| rs576854155 | 17:7,849,062 | C/T | — | uncertain significance |
| rs774012754 | 17:7,849,083 | A/C | — | uncertain significance |
| rs780307478 | 17:7,849,111 | G/T | — | uncertain significance |
| rs753613469 | 17:7,849,175 | G/A | — | uncertain significance |
| rs2545372793 | 17:7,849,203 | G/T | — | uncertain significance |
| rs190029027 | 17:7,849,220 | C/G | — | uncertain significance |
| rs757744124 | 17:7,849,299 | C/A | — | uncertain significance |
| rs1974697793 | 17:7,850,917 | C/G | — | uncertain significance |
| rs76262783 | 17:7,850,972 | G/A | — | uncertain significance |
| rs74595649 | 17:7,851,278 | C/T | — | likely benign |
| rs377378521 | 17:7,851,288 | C/G | — | uncertain significance |
| rs377547989 | 17:7,851,529 | C/T | — | uncertain significance |
| rs370474872 | 17:7,851,579 | C/T | — | uncertain significance |
| rs1030751852 | 17:7,851,589 | A/C | — | uncertain significance |
| rs551139444 | 17:7,851,873 | C/T | — | uncertain significance |
| rs201279797 | 17:7,851,924 | C/G | — | uncertain significance |
| rs563908709 | 17:7,851,935 | C/G | — | uncertain significance |
| rs758365980 | 17:7,851,991 | G/A | — | uncertain significance |
| rs772223052 | 17:7,852,721 | C/T | — | uncertain significance |
| rs754323785 | 17:7,852,725 | G/A | — | uncertain significance |
| rs140158283 | 17:7,852,727 | C/T | — | uncertain significance |
| rs538266374 | 17:7,852,728 | G/A | — | uncertain significance |
| rs530637849 | 17:7,852,762 | C/T | — | likely benign |
| rs371383062 | 17:7,852,767 | G/A | — | uncertain significance |
| rs1555630929 | 17:7,852,808 | C/T | — | uncertain significance |
| rs757139029 | 17:7,852,815 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.