CDC20
cell division cycle 20
Summary
CDC20 appears to act as a regulatory protein interacting with several other proteins at multiple points in the cell cycle. It is required for two microtubule-dependent processes, nuclear movement prior to anaphase and chromosome separation. [provided by RefSeq, Jul 2008]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs866946379 | 1:43,824,974 | C/A | — | uncertain significance |
| rs1188441660 | 1:43,824,995 | G/A | — | uncertain significance |
| rs1647161130 | 1:43,825,281 | C/T | — | uncertain significance |
| rs373153778 | 1:43,825,283 | G/C | — | uncertain significance |
| rs760334505 | 1:43,825,310 | G/A | — | pathogenic |
| rs1225329364 | 1:43,825,401 | T/A | — | uncertain significance |
| rs144561572 | 1:43,825,484 | C/T | — | uncertain significance |
| rs201827674 | 1:43,825,681 | A/C | — | uncertain significance |
| rs781443151 | 1:43,825,696 | C/G | — | uncertain significance |
| rs372598188 | 1:43,825,729 | G/C | — | uncertain significance |
| rs2545698654 | 1:43,825,756 | C/T | — | pathogenic |
| rs752709238 | 1:43,825,769 | G/T | — | likely pathogenic |
| rs2545698940 | 1:43,825,938 | G/A | — | pathogenic |
| rs1309457938 | 1:43,825,990 | A/G | — | pathogenic |
| rs2545699030 | 1:43,826,032 | C/T | — | uncertain significance |
| rs754957702 | 1:43,826,200 | C/T | — | pathogenic |
| rs991296026 | 1:43,826,411 | C/A | — | uncertain significance |
| rs2545699601 | 1:43,826,432 | C/T | — | uncertain significance |
| rs763960946 | 1:43,826,501 | C/T | — | uncertain significance |
| rs372597302 | 1:43,826,519 | C/T | — | pathogenic |
| rs140305765 | 1:43,826,520 | G/A | — | pathogenic |
| rs749421572 | 1:43,826,573 | C/A | — | uncertain significance |
| rs2545699849 | 1:43,826,627 | G/A | — | uncertain significance |
| rs1801456 | 1:43,826,794 | G/A | — | likely benign |
| rs2545700034 | 1:43,826,800 | T/C | — | uncertain significance |
| rs368676792 | 1:43,826,819 | A/G | — | uncertain significance |
| rs757848486 | 1:43,826,868 | G/C | — | pathogenic |
| rs1172992921 | 1:43,826,900 | T/G | — | uncertain significance |
| rs1319289274 | 1:43,827,957 | C/T | — | uncertain significance |
| rs779630788 | 1:43,828,642 | A/G | — | uncertain significance |
| rs746457353 | 1:43,828,646 | T/C | — | uncertain significance |
| rs150849773 | 1:43,828,651 | A/G | — | uncertain significance |
| rs760038301 | 1:43,828,670 | C/T | — | uncertain significance |
| rs761756771 | 1:43,828,711 | C/T | — | uncertain significance |
| rs45461499 | 1:43,828,736 | G/A | missense variant | — |
| rs746179756 | 1:43,828,738 | C/T | — | uncertain significance |
| rs759288917 | 1:43,828,742 | G/C | — | uncertain significance |
| rs377329238 | 1:43,828,747 | C/T | — | uncertain significance |
| rs2069388 | 1:43,828,752 | G/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.