ZW10
zw10 kinetochore protein
Summary
This gene encodes a protein that is one of many involved in mechanisms to ensure proper chromosome segregation during cell division. This protein is an essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. [provided by RefSeq, Aug 2011]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs144914370 | 11:113,604,449 | T/G | — | uncertain significance |
| rs749505110 | 11:113,604,471 | C/T | — | uncertain significance |
| rs183043300 | 11:113,604,907 | A/G | intron variant | — |
| rs143270930 | 11:113,605,075 | C/T | intron variant | — |
| rs753707596 | 11:113,607,442 | T/C | — | uncertain significance |
| rs1953557497 | 11:113,607,459 | G/A | — | uncertain significance |
| rs201244304 | 11:113,608,991 | G/A | — | uncertain significance |
| rs1448539932 | 11:113,609,063 | T/C | — | uncertain significance |
| rs2547068106 | 11:113,609,986 | A/G | — | uncertain significance |
| rs1445975390 | 11:113,610,032 | C/A | — | uncertain significance |
| rs748169308 | 11:113,610,054 | C/G | — | uncertain significance |
| rs375534081 | 11:113,614,567 | C/T | — | uncertain significance |
| rs1043963710 | 11:113,614,602 | C/T | — | uncertain significance |
| rs200000547 | 11:113,614,711 | C/A | — | uncertain significance |
| rs752104149 | 11:113,614,716 | T/C | — | uncertain significance |
| rs2271261 | 11:113,618,936 | A/T | downstream gene variant | — |
| rs768843839 | 11:113,619,122 | G/T | — | uncertain significance |
| rs73007975 | 11:113,620,210 | G/A | downstream gene variant | — |
| rs2547073902 | 11:113,628,464 | G/A | — | uncertain significance |
| rs202061176 | 11:113,628,482 | C/T | — | uncertain significance |
| rs1953808679 | 11:113,628,566 | A/C | — | uncertain significance |
| rs759450154 | 11:113,629,311 | A/G | — | uncertain significance |
| rs757238012 | 11:113,629,335 | C/A | — | uncertain significance |
| rs1478093487 | 11:113,629,348 | T/C | — | likely benign |
| rs767509174 | 11:113,629,396 | C/T | — | uncertain significance |
| rs199649706 | 11:113,629,404 | A/G | — | uncertain significance |
| rs570046920 | 11:113,629,957 | C/T | — | — |
| rs1343176194 | 11:113,631,048 | C/A | — | uncertain significance |
| rs138036646 | 11:113,631,060 | T/C | — | uncertain significance |
| rs200622589 | 11:113,631,245 | C/T | — | likely benign |
| rs544769818 | 11:113,631,246 | G/A | — | uncertain significance |
| rs1953846806 | 11:113,631,293 | T/C | — | uncertain significance |
| rs200704105 | 11:113,631,613 | C/T | — | uncertain significance |
| rs201149106 | 11:113,639,628 | G/A | — | uncertain significance |
| rs61905747 | 11:113,639,842 | A/C | downstream gene variant | — |
| rs2459976 | 11:113,642,993 | G/A | upstream gene variant | — |
| rs1266684950 | 11:113,644,356 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.