NEK9
NIMA related kinase 9
Summary
This gene encodes a member of the NimA (never in mitosis A) family of serine/threonine protein kinases. The encoded protein is activated in mitosis and, in turn, activates other family members during mitosis. This protein also mediates cellular processes that are essential for interphase progression. [provided by RefSeq, Jul 2016]
Known Variants119 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs175487 | 14:75,551,254 | C/T | — | benign |
| rs61745420 | 14:75,551,321 | T/G | — | benign |
| rs377136228 | 14:75,551,326 | C/A | — | uncertain significance |
| rs766946654 | 14:75,551,353 | C/T | — | uncertain significance |
| rs1893965717 | 14:75,551,381 | C/T | — | uncertain significance |
| rs175486 | 14:75,551,442 | A/C | — | benign |
| rs175485 | 14:75,553,655 | T/C | — | benign |
| rs150013785 | 14:75,553,765 | T/C | — | uncertain significance |
| rs2503447053 | 14:75,553,829 | C/G | — | uncertain significance |
| rs201030660 | 14:75,553,879 | G/T | — | uncertain significance |
| rs2503447513 | 14:75,553,921 | T/C | — | uncertain significance |
| rs749642426 | 14:75,553,923 | A/G | — | uncertain significance |
| rs774587035 | 14:75,553,930 | G/T | — | uncertain significance |
| rs1171410135 | 14:75,555,271 | T/C | — | uncertain significance |
| rs36014869 | 14:75,555,305 | G/T | — | benign |
| rs73309781 | 14:75,555,490 | C/A | — | benign |
| rs200445076 | 14:75,557,969 | T/C | — | likely benign |
| rs1594824169 | 14:75,557,981 | G/A | — | uncertain significance |
| rs1237087089 | 14:75,557,992 | C/T | — | uncertain significance |
| rs140661298 | 14:75,558,030 | T/C | — | likely benign |
| rs114347531 | 14:75,558,058 | C/T | — | likely benign |
| rs2503458817 | 14:75,558,139 | C/T | — | uncertain significance |
| rs777758507 | 14:75,558,140 | C/T | — | likely benign |
| rs1273011500 | 14:75,558,143 | C/T | — | uncertain significance |
| rs149468885 | 14:75,558,144 | G/A | — | benign |
| rs34648344 | 14:75,558,152 | C/T | — | benign |
| rs2503459108 | 14:75,558,176 | G/A | — | pathogenic |
| rs8022874 | 14:75,558,231 | A/C | — | benign |
| rs7142235 | 14:75,559,963 | T/G | — | — |
| rs175479 | 14:75,561,871 | A/C | — | benign |
| rs61746426 | 14:75,562,076 | A/G | — | conflicting classifications of pathogenicity |
| rs1282735715 | 14:75,562,096 | T/G | — | uncertain significance |
| rs147395825 | 14:75,563,805 | A/G | — | uncertain significance |
| rs748222443 | 14:75,563,830 | G/A | — | uncertain significance |
| rs1402196530 | 14:75,563,875 | G/A | — | likely pathogenic |
| rs1413266993 | 14:75,563,908 | G/T | — | uncertain significance |
| rs142859694 | 14:75,563,934 | C/T | missense variant | pathogenic |
| rs375939813 | 14:75,563,935 | G/A | — | uncertain significance |
| rs115060381 | 14:75,567,529 | G/C | — | benign |
| rs2503481568 | 14:75,567,738 | G/C | — | uncertain significance |
| rs375873968 | 14:75,567,847 | C/T | — | uncertain significance |
| rs778413122 | 14:75,567,854 | G/A | — | pathogenic |
| rs4899545 | 14:75,568,138 | A/G | — | benign |
| rs146787666 | 14:75,568,358 | A/G | — | conflicting classifications of pathogenicity |
| rs201574563 | 14:75,568,393 | C/A | — | uncertain significance |
| rs200363570 | 14:75,568,401 | C/T | — | uncertain significance |
| rs1894588127 | 14:75,568,416 | G/A | — | uncertain significance |
| rs201240335 | 14:75,568,434 | G/A | — | uncertain significance |
| rs140694625 | 14:75,568,461 | T/A | — | uncertain significance |
| rs78868109 | 14:75,568,499 | A/G | — | benign |
| rs56995742 | 14:75,570,528 | C/A | — | benign |
| rs886037838 | 14:75,570,544 | C/A | — | pathogenic |
| rs1555352529 | 14:75,570,558 | A/G | — | pathogenic |
| rs886037839 | 14:75,570,561 | C/A | missense variant | pathogenic |
| rs771058935 | 14:75,570,654 | C/G | — | uncertain significance |
| rs119077 | 14:75,572,559 | T/C | — | benign |
| rs145329238 | 14:75,573,203 | A/G | — | uncertain significance |
| rs149201547 | 14:75,573,220 | C/T | — | uncertain significance |
| rs534245464 | 14:75,573,228 | T/C | — | likely benign |
| rs757011098 | 14:75,573,244 | G/A | stop gained | pathogenic |
| rs1894787169 | 14:75,573,346 | C/G | — | uncertain significance |
| rs1362564667 | 14:75,573,366 | C/T | — | likely pathogenic |
| rs17093920 | 14:75,573,525 | T/C | — | benign |
| rs2503501853 | 14:75,574,044 | A/G | — | likely pathogenic |
| rs1327520738 | 14:75,574,045 | C/A | — | likely pathogenic |
| rs143529818 | 14:75,574,047 | A/G | — | likely benign |
| rs10146482 | 14:75,574,087 | C/T | — | benign |
| rs770976408 | 14:75,574,137 | G/A | — | likely benign |
| rs370474070 | 14:75,576,444 | C/T | — | likely benign |
| rs377370182 | 14:75,576,456 | G/A | — | uncertain significance |
| rs8005071 | 14:75,576,520 | A/G | — | benign |
| rs1237535497 | 14:75,576,537 | G/A | — | pathogenic |
| rs371822393 | 14:75,576,580 | C/T | — | likely benign |
| rs750027769 | 14:75,577,027 | G/A | — | uncertain significance |
| rs2503517545 | 14:75,580,060 | A/C | — | uncertain significance |
| rs1057518379 | 14:75,580,072 | A/G | missense variant | pathogenic |
| rs1895020933 | 14:75,580,108 | T/C | — | likely pathogenic |
| rs175464 | 14:75,580,152 | G/A | — | benign |
| rs143703209 | 14:75,580,918 | C/T | — | likely benign |
| rs751357379 | 14:75,580,951 | C/G | — | uncertain significance |
| rs779226121 | 14:75,580,989 | C/T | — | uncertain significance |
| rs111316318 | 14:75,583,888 | G/A | — | conflicting classifications of pathogenicity |
| rs901508820 | 14:75,583,933 | C/A | stop gained | pathogenic |
| rs752811634 | 14:75,585,533 | C/T | — | uncertain significance |
| rs781646268 | 14:75,585,633 | A/G | — | uncertain significance |
| rs12883497 | 14:75,587,014 | G/A | — | benign |
| rs879253775 | 14:75,587,237 | A/G | missense variant | pathogenic |
| rs200004115 | 14:75,587,251 | T/C | — | likely benign |
| rs73311631 | 14:75,587,339 | T/C | — | benign |
| rs175454 | 14:75,587,351 | T/C | — | benign |
| rs2139806574 | 14:75,587,870 | G/T | — | uncertain significance |
| rs114680267 | 14:75,590,722 | G/A | — | benign |
| rs781664727 | 14:75,590,778 | G/A | — | uncertain significance |
| rs375063665 | 14:75,590,786 | G/A | — | likely benign |
| rs8017642 | 14:75,590,822 | G/A | — | benign |
| rs175449 | 14:75,590,846 | A/T | — | benign |
| rs562180803 | 14:75,590,882 | C/G | — | benign |
| rs143597394 | 14:75,590,896 | C/T | — | likely benign |
| rs202032678 | 14:75,590,924 | A/G | — | benign |
| rs175448 | 14:75,591,071 | G/A | — | benign |
Showing 100 of 119 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.