KIFC1
kinesin family member C1
Summary
Predicted to enable ATP hydrolysis activity; microtubule binding activity; and minus-end-directed microtubule motor activity. Involved in mitotic metaphase chromosome alignment and mitotic spindle assembly. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs211458 | 6:33,365,353 | A/G | downstream gene variant | — |
| rs761304186 | 6:33,365,812 | C/T | — | uncertain significance |
| rs777679851 | 6:33,365,837 | T/C | — | likely benign |
| rs745748227 | 6:33,365,863 | G/T | — | uncertain significance |
| rs145995335 | 6:33,365,907 | G/T | — | uncertain significance |
| rs201829505 | 6:33,366,068 | C/T | — | uncertain significance |
| rs2537108918 | 6:33,371,114 | G/C | — | uncertain significance |
| rs778542683 | 6:33,371,598 | C/G | — | uncertain significance |
| rs566475584 | 6:33,371,866 | A/T | — | uncertain significance |
| rs755047662 | 6:33,371,872 | G/A | — | uncertain significance |
| rs144374629 | 6:33,371,878 | G/T | — | uncertain significance |
| rs147923884 | 6:33,372,651 | C/T | — | uncertain significance |
| rs756078114 | 6:33,372,713 | G/A | — | likely benign |
| rs562615563 | 6:33,372,728 | C/T | — | uncertain significance |
| rs147773024 | 6:33,372,738 | G/A | — | uncertain significance |
| rs138661437 | 6:33,372,837 | C/T | — | uncertain significance |
| rs1314781127 | 6:33,372,866 | C/T | — | uncertain significance |
| rs754463582 | 6:33,372,912 | G/A | — | likely benign |
| rs769727957 | 6:33,372,938 | C/T | — | uncertain significance |
| rs1775580610 | 6:33,372,954 | G/T | — | uncertain significance |
| rs371098598 | 6:33,372,968 | C/A | — | uncertain significance |
| rs779239713 | 6:33,372,974 | A/G | — | uncertain significance |
| rs1775583493 | 6:33,372,993 | T/G | — | uncertain significance |
| rs777141893 | 6:33,373,006 | C/G | — | uncertain significance |
| rs2537118367 | 6:33,373,010 | C/T | — | uncertain significance |
| rs147520254 | 6:33,373,200 | C/G | — | uncertain significance |
| rs752546936 | 6:33,373,238 | A/C | — | uncertain significance |
| rs372177506 | 6:33,373,257 | T/C | — | uncertain significance |
| rs148425649 | 6:33,373,338 | G/A | — | likely benign |
| rs555069021 | 6:33,373,365 | C/T | — | likely benign |
| rs2537124064 | 6:33,373,977 | A/G | — | uncertain significance |
| rs772206166 | 6:33,373,998 | G/A | — | likely benign |
| rs754974858 | 6:33,374,037 | G/A | — | uncertain significance |
| rs1315007008 | 6:33,374,094 | G/A | — | uncertain significance |
| rs778110898 | 6:33,374,105 | T/C | — | uncertain significance |
| rs201789629 | 6:33,374,171 | G/A | — | uncertain significance |
| rs751948529 | 6:33,374,184 | G/T | — | uncertain significance |
| rs2537125671 | 6:33,374,214 | A/T | — | uncertain significance |
| rs985318176 | 6:33,374,387 | C/T | — | uncertain significance |
| rs570228172 | 6:33,374,606 | A/G | — | uncertain significance |
| rs56369265 | 6:33,375,130 | G/A | regulatory region variant | — |
| rs758476704 | 6:33,377,456 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.