CNTRL
centriolin
Summary
This gene encodes a centrosomal protein required for the centrosome to function as a microtubule organizing center. The gene product is also associated with centrosome maturation. One version of stem cell myeloproliferative disorder is the result of a reciprocal translocation between chromosomes 8 and 9, with the breakpoint associated with fibroblast growth factor receptor 1 and centrosomal protein 1. [provided by RefSeq, Jul 2008]
Known Variants139 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7856420 | 9:123,839,157 | G/A | — | — |
| rs113179388 | 9:123,849,924 | G/A | intron variant | — |
| rs1244530507 | 9:123,850,636 | C/A | — | uncertain significance |
| rs147018954 | 9:123,850,642 | C/A | — | likely benign |
| rs532419601 | 9:123,850,683 | A/G | — | uncertain significance |
| rs376813167 | 9:123,850,786 | A/G | — | uncertain significance |
| rs201927709 | 9:123,850,816 | A/G | — | uncertain significance |
| rs1374715713 | 9:123,852,628 | C/T | — | uncertain significance |
| rs117390062 | 9:123,852,665 | C/T | — | benign |
| rs140149582 | 9:123,852,666 | G/A | — | uncertain significance |
| rs560865457 | 9:123,857,266 | G/A | — | uncertain significance |
| rs143778395 | 9:123,858,807 | G/A | — | uncertain significance |
| rs376193404 | 9:123,858,840 | C/T | — | uncertain significance |
| rs144772143 | 9:123,860,679 | A/C | — | uncertain significance |
| rs143362843 | 9:123,860,696 | A/G | — | benign |
| rs150932215 | 9:123,860,749 | A/G | — | uncertain significance |
| rs764835008 | 9:123,860,761 | C/G | — | uncertain significance |
| rs1370903218 | 9:123,870,121 | A/G | — | uncertain significance |
| rs747122850 | 9:123,870,151 | A/G | — | uncertain significance |
| rs1174581971 | 9:123,870,226 | C/G | — | uncertain significance |
| rs1051076890 | 9:123,874,816 | T/C | — | uncertain significance |
| rs752707957 | 9:123,875,781 | A/G | — | uncertain significance |
| rs149113705 | 9:123,875,820 | T/C | — | uncertain significance |
| rs2541107491 | 9:123,875,835 | A/T | — | uncertain significance |
| rs200760374 | 9:123,875,844 | A/G | — | uncertain significance |
| rs142008519 | 9:123,875,949 | G/A | — | uncertain significance |
| rs547352269 | 9:123,875,967 | C/T | — | uncertain significance |
| rs1415895882 | 9:123,875,979 | A/G | — | uncertain significance |
| rs200058562 | 9:123,877,478 | G/A | — | likely benign |
| rs201982083 | 9:123,880,640 | A/G | — | uncertain significance |
| rs777914830 | 9:123,880,644 | C/A | — | uncertain significance |
| rs150881178 | 9:123,880,666 | G/A | — | uncertain significance |
| rs75531179 | 9:123,880,694 | G/A | — | benign |
| rs776155552 | 9:123,880,714 | G/C | — | uncertain significance |
| rs144178223 | 9:123,880,790 | A/T | — | likely benign |
| rs1367077791 | 9:123,886,231 | G/A | — | uncertain significance |
| rs373638859 | 9:123,886,284 | A/T | — | uncertain significance |
| rs2541385246 | 9:123,888,035 | G/A | — | uncertain significance |
| rs367624022 | 9:123,888,129 | A/C | — | uncertain significance |
| rs942355055 | 9:123,888,197 | G/A | — | uncertain significance |
| rs2541583911 | 9:123,898,108 | C/T | — | uncertain significance |
| rs2541587736 | 9:123,898,252 | C/G | — | uncertain significance |
| rs79192016 | 9:123,898,259 | A/G | — | benign |
| rs566495778 | 9:123,900,898 | T/A | — | uncertain significance |
| rs200179809 | 9:123,902,995 | G/A | — | likely benign |
| rs149378709 | 9:123,903,000 | G/A | — | uncertain significance |
| rs148151065 | 9:123,903,015 | C/T | — | uncertain significance |
| rs141938357 | 9:123,903,016 | G/A | — | uncertain significance |
| rs2051461775 | 9:123,903,024 | G/A | — | uncertain significance |
| rs200395989 | 9:123,903,732 | C/T | — | uncertain significance |
| rs1161619502 | 9:123,903,762 | G/A | — | uncertain significance |
| rs1026976164 | 9:123,903,782 | A/C | — | uncertain significance |
| rs548663694 | 9:123,904,003 | T/C | — | — |
| rs1288910297 | 9:123,904,507 | A/G | — | uncertain significance |
| rs148672807 | 9:123,904,538 | T/C | — | benign |
| rs201327336 | 9:123,906,221 | G/A | — | uncertain significance |
| rs373344449 | 9:123,906,307 | C/G | — | uncertain significance |
| rs1466230583 | 9:123,906,311 | T/C | — | uncertain significance |
| rs1393995102 | 9:123,906,322 | C/T | — | uncertain significance |
| rs1440344579 | 9:123,907,184 | G/A | — | uncertain significance |
| rs138200958 | 9:123,907,535 | T/C | — | uncertain significance |
| rs1259748874 | 9:123,907,610 | G/A | — | uncertain significance |
| rs767269657 | 9:123,908,434 | G/A | — | uncertain significance |
| rs368623219 | 9:123,908,508 | T/A | — | uncertain significance |
| rs35342437 | 9:123,908,511 | A/G | — | uncertain significance |
| rs563687818 | 9:123,908,517 | C/T | — | uncertain significance |
| rs192079395 | 9:123,908,523 | C/T | — | likely benign |
| rs1343960629 | 9:123,910,974 | A/T | — | uncertain significance |
| rs754136974 | 9:123,911,110 | G/A | — | uncertain significance |
| rs563584469 | 9:123,911,137 | G/T | — | uncertain significance |
| rs2134207043 | 9:123,912,498 | G/C | — | uncertain significance |
| rs146245097 | 9:123,912,534 | A/G | — | uncertain significance |
| rs144171493 | 9:123,912,576 | A/G | — | uncertain significance |
| rs146512881 | 9:123,912,579 | G/A | — | uncertain significance |
| rs2052150916 | 9:123,912,591 | C/T | — | uncertain significance |
| rs1588269496 | 9:123,912,593 | A/G | — | likely benign |
| rs770226863 | 9:123,912,619 | G/A | — | likely benign |
| rs371013564 | 9:123,912,649 | G/T | — | uncertain significance |
| rs2538975274 | 9:123,912,657 | C/G | — | uncertain significance |
| rs558014706 | 9:123,912,694 | C/G | — | likely benign |
| rs151124524 | 9:123,914,765 | G/T | — | benign |
| rs2539016112 | 9:123,914,799 | C/G | — | uncertain significance |
| rs773330321 | 9:123,914,837 | A/C | — | uncertain significance |
| rs16910366 | 9:123,914,840 | A/G | — | benign |
| rs574338866 | 9:123,914,854 | C/T | — | uncertain significance |
| rs9408926 | 9:123,914,874 | C/T | synonymous variant | — |
| rs372575690 | 9:123,914,881 | A/G | — | uncertain significance |
| rs375930484 | 9:123,914,907 | A/C | — | uncertain significance |
| rs769404106 | 9:123,917,050 | A/G | — | likely benign |
| rs1225097148 | 9:123,917,118 | G/A | — | uncertain significance |
| rs144738756 | 9:123,917,145 | G/C | — | likely benign |
| rs751035332 | 9:123,920,020 | C/T | — | likely benign |
| rs2539106626 | 9:123,920,053 | A/T | — | uncertain significance |
| rs144086611 | 9:123,920,122 | A/C | — | conflicting classifications of pathogenicity |
| rs200841631 | 9:123,920,284 | T/C | — | uncertain significance |
| rs149734346 | 9:123,920,304 | G/A | — | uncertain significance |
| rs777271960 | 9:123,922,556 | A/G | — | likely benign |
| rs1410394387 | 9:123,922,561 | G/C | — | uncertain significance |
| rs749544191 | 9:123,924,173 | A/G | — | uncertain significance |
| rs749905942 | 9:123,924,401 | C/G | — | uncertain significance |
Showing 100 of 139 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.