KIF15
kinesin family member 15
Summary
Predicted to enable ATP hydrolysis activity; microtubule binding activity; and plus-end-directed microtubule motor activity. Predicted to be involved in centrosome separation; microtubule-based movement; and mitotic spindle assembly. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants91 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs113187813 | 3:44,808,716 | C/T | intron variant | — |
| rs188264700 | 3:44,813,116 | A/T | intron variant | — |
| rs372949327 | 3:44,815,903 | G/A | — | likely benign |
| rs1210206970 | 3:44,816,746 | T/G | — | uncertain significance |
| rs34893204 | 3:44,816,758 | T/A | — | uncertain significance |
| rs779615762 | 3:44,816,777 | C/T | — | likely risk allele |
| rs201923210 | 3:44,816,778 | G/A | — | likely risk allele |
| rs2528970315 | 3:44,816,847 | C/T | — | likely risk allele |
| rs147576633 | 3:44,816,853 | C/T | — | uncertain significance |
| rs375356443 | 3:44,816,895 | C/T | — | likely benign |
| rs745815466 | 3:44,819,618 | C/T | — | likely benign |
| rs199704142 | 3:44,819,652 | A/G | — | uncertain significance |
| rs769971786 | 3:44,822,408 | A/G | — | uncertain significance |
| rs549556281 | 3:44,826,336 | G/A | — | likely risk allele |
| rs1247963130 | 3:44,826,384 | C/T | — | likely risk allele |
| rs761190372 | 3:44,826,388 | G/A | — | uncertain significance |
| rs143787591 | 3:44,827,912 | G/C | — | likely benign |
| rs2529062512 | 3:44,828,022 | G/A | — | uncertain significance |
| rs34862960 | 3:44,828,059 | C/T | — | likely benign |
| rs778582710 | 3:44,835,729 | G/T | — | uncertain significance |
| rs758022463 | 3:44,835,742 | G/A | — | likely risk allele |
| rs746830048 | 3:44,835,754 | A/G | — | uncertain significance |
| rs145798160 | 3:44,835,784 | G/A | — | uncertain significance |
| rs931316762 | 3:44,839,143 | A/G | — | uncertain significance |
| rs763859357 | 3:44,839,408 | C/T | — | uncertain significance |
| rs2529148806 | 3:44,839,425 | A/G | — | uncertain significance |
| rs374356897 | 3:44,841,809 | G/A | — | uncertain significance |
| rs113767782 | 3:44,841,883 | G/C | — | benign |
| rs72875734 | 3:44,842,943 | C/A | — | benign |
| rs138660634 | 3:44,843,362 | C/T | — | uncertain significance |
| rs72875737 | 3:44,843,440 | A/G | — | benign |
| rs1002572191 | 3:44,843,458 | C/T | — | pathogenic |
| rs148546332 | 3:44,844,424 | C/G | — | uncertain significance |
| rs749806165 | 3:44,846,598 | G/C | — | likely benign |
| rs80059929 | 3:44,846,722 | T/A | intron variant | — |
| rs2529223639 | 3:44,847,335 | A/C | — | likely pathogenic |
| rs201266748 | 3:44,847,372 | C/T | — | uncertain significance |
| rs1005517209 | 3:44,847,410 | G/A | — | uncertain significance |
| rs1401015169 | 3:44,847,416 | A/G | — | uncertain significance |
| rs2529225574 | 3:44,847,469 | A/T | — | uncertain significance |
| rs1489335976 | 3:44,852,443 | A/G | — | uncertain significance |
| rs755867116 | 3:44,852,510 | T/C | — | uncertain significance |
| rs180766229 | 3:44,854,560 | C/T | — | benign |
| rs76971569 | 3:44,854,614 | T/G | — | benign |
| rs2529275842 | 3:44,854,618 | T/C | — | uncertain significance |
| rs2529287158 | 3:44,856,438 | C/T | — | uncertain significance |
| rs765988858 | 3:44,856,447 | G/A | — | uncertain significance |
| rs74888477 | 3:44,856,496 | C/T | — | uncertain significance |
| rs77079961 | 3:44,856,499 | A/G | — | benign |
| rs2529287904 | 3:44,856,510 | G/A | — | uncertain significance |
| rs764788641 | 3:44,856,549 | C/G | — | uncertain significance |
| rs141979279 | 3:44,858,131 | T/C | intron variant | — |
| rs59678460 | 3:44,867,525 | A/G | — | benign |
| rs114793043 | 3:44,867,592 | C/T | — | uncertain significance |
| rs2529394212 | 3:44,867,867 | A/C | — | uncertain significance |
| rs112882527 | 3:44,868,976 | G/A | — | conflicting classifications of pathogenicity |
| rs747160107 | 3:44,868,980 | G/A | — | uncertain significance |
| rs142345690 | 3:44,870,765 | C/A | — | — |
| rs147698358 | 3:44,871,524 | C/T | — | uncertain significance |
| rs148787580 | 3:44,872,381 | T/C | — | benign |
| rs377167940 | 3:44,872,447 | G/C | — | uncertain significance |
| rs34791294 | 3:44,872,450 | A/G | — | benign |
| rs148155714 | 3:44,879,770 | G/A | — | uncertain significance |
| rs138611262 | 3:44,879,843 | C/T | — | benign |
| rs146195393 | 3:44,879,846 | G/A | — | uncertain significance |
| rs756658896 | 3:44,879,876 | C/T | — | uncertain significance |
| rs149445851 | 3:44,881,887 | A/G | — | uncertain significance |
| rs1217109848 | 3:44,881,928 | T/C | — | uncertain significance |
| rs777570812 | 3:44,882,564 | A/G | — | likely risk allele |
| rs80007780 | 3:44,882,586 | C/G | — | benign |
| rs1164871307 | 3:44,882,608 | C/T | — | uncertain significance |
| rs144715957 | 3:44,882,620 | C/G | — | uncertain significance |
| rs754722890 | 3:44,882,672 | T/C | — | uncertain significance |
| rs766965765 | 3:44,884,644 | C/T | — | uncertain significance |
| rs149974125 | 3:44,884,645 | G/T | — | uncertain significance |
| rs1362729507 | 3:44,884,651 | A/G | — | uncertain significance |
| rs199665568 | 3:44,884,665 | A/G | — | uncertain significance |
| rs775000463 | 3:44,884,705 | T/A | — | uncertain significance |
| rs1201287181 | 3:44,889,515 | A/C | — | uncertain significance |
| rs199928777 | 3:44,889,517 | C/A | — | uncertain significance |
| rs747643201 | 3:44,893,287 | A/T | — | uncertain significance |
| rs17076986 | 3:44,893,288 | A/C | — | benign |
| rs2529639846 | 3:44,893,335 | C/T | — | uncertain significance |
| rs148526731 | 3:44,893,346 | G/A | — | uncertain significance |
| rs964461953 | 3:44,893,349 | C/A | — | likely benign |
| rs1301803598 | 3:44,893,747 | T/G | — | uncertain significance |
| rs2529642839 | 3:44,893,756 | G/C | — | uncertain significance |
| rs2529646767 | 3:44,894,172 | A/G | — | uncertain significance |
| rs184866086 | 3:44,894,185 | C/T | — | benign |
| rs78238620 | 3:44,902,386 | T/A | upstream gene variant | — |
| rs2292181 | 3:44,903,434 | G/C | synonymous variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.