KNTC1
kinetochore associated 1
Summary
This gene encodes a protein that is one of many involved in mechanisms to ensure proper chromosome segregation during cell division. Experimental evidence indicated that the encoded protein functioned in a similar manner to that of the Drosophila rough deal protein. [provided by RefSeq, Jul 2008]
Known Variants90 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs770102985 | 12:123,014,618 | A/G | — | uncertain significance |
| rs61751319 | 12:123,014,650 | G/A | — | uncertain significance |
| rs61752342 | 12:123,014,705 | A/G | — | uncertain significance |
| rs770442709 | 12:123,019,318 | G/C | — | uncertain significance |
| rs751383353 | 12:123,022,931 | T/C | — | uncertain significance |
| rs1962018074 | 12:123,022,937 | T/C | — | uncertain significance |
| rs971928204 | 12:123,022,942 | G/A | — | uncertain significance |
| rs1468032148 | 12:123,022,978 | T/A | — | uncertain significance |
| rs775527571 | 12:123,024,253 | C/T | — | uncertain significance |
| rs1221608471 | 12:123,024,287 | A/G | — | uncertain significance |
| rs6489071 | 12:123,025,576 | C/T | — | — |
| rs781099032 | 12:123,026,606 | A/C | — | uncertain significance |
| rs185354191 | 12:123,026,621 | C/T | — | uncertain significance |
| rs968385497 | 12:123,028,171 | C/G | — | uncertain significance |
| rs776903535 | 12:123,032,017 | C/T | — | uncertain significance |
| rs1465273348 | 12:123,032,467 | G/A | — | uncertain significance |
| rs549673609 | 12:123,036,049 | C/A | — | uncertain significance |
| rs375661591 | 12:123,041,932 | T/C | — | uncertain significance |
| rs2547388265 | 12:123,041,965 | A/G | — | uncertain significance |
| rs143555331 | 12:123,042,005 | C/T | — | likely benign |
| rs779516600 | 12:123,042,055 | A/G | — | uncertain significance |
| rs371401714 | 12:123,042,178 | A/G | — | uncertain significance |
| rs10773302 | 12:123,043,145 | G/T | intron variant | — |
| rs2547398588 | 12:123,046,489 | A/G | — | uncertain significance |
| rs773891168 | 12:123,047,185 | G/A | — | uncertain significance |
| rs1165218113 | 12:123,047,200 | G/A | — | uncertain significance |
| rs6489111 | 12:123,051,018 | A/G | upstream gene variant | — |
| rs192844811 | 12:123,054,327 | A/G | — | uncertain significance |
| rs2547423493 | 12:123,057,494 | A/C | — | uncertain significance |
| rs374239725 | 12:123,057,725 | A/G | — | uncertain significance |
| rs367576553 | 12:123,057,786 | G/T | — | uncertain significance |
| rs201148456 | 12:123,058,923 | C/T | — | uncertain significance |
| rs1593584867 | 12:123,060,183 | G/T | — | uncertain significance |
| rs1964977143 | 12:123,060,379 | T/C | — | uncertain significance |
| rs200445300 | 12:123,060,384 | A/T | — | uncertain significance |
| rs764354490 | 12:123,060,413 | A/G | — | uncertain significance |
| rs202085825 | 12:123,061,452 | G/A | — | uncertain significance |
| rs183574130 | 12:123,061,479 | C/A | — | uncertain significance |
| rs779089672 | 12:123,061,490 | G/A | — | uncertain significance |
| rs2547432521 | 12:123,061,523 | T/C | — | likely benign |
| rs917175141 | 12:123,061,524 | C/A | — | uncertain significance |
| rs201402164 | 12:123,062,253 | C/T | — | uncertain significance |
| rs201981485 | 12:123,067,303 | G/T | — | uncertain significance |
| rs1437220161 | 12:123,067,408 | A/G | — | uncertain significance |
| rs1160739010 | 12:123,067,442 | C/T | — | uncertain significance |
| rs1419972138 | 12:123,068,866 | T/G | — | uncertain significance |
| rs1038774403 | 12:123,069,487 | G/A | — | uncertain significance |
| rs377094070 | 12:123,070,273 | G/A | — | uncertain significance |
| rs372672248 | 12:123,071,250 | A/G | — | uncertain significance |
| rs267603355 | 12:123,072,287 | T/C | — | uncertain significance |
| rs148599474 | 12:123,073,346 | A/G | — | uncertain significance |
| rs61954974 | 12:123,074,169 | T/C | intron variant | — |
| rs146677327 | 12:123,074,487 | C/T | intron variant | — |
| rs2547462345 | 12:123,075,975 | G/T | — | uncertain significance |
| rs369735435 | 12:123,075,990 | G/A | — | uncertain significance |
| rs761008447 | 12:123,078,886 | G/C | — | uncertain significance |
| rs200503296 | 12:123,078,902 | T/G | — | uncertain significance |
| rs750091974 | 12:123,082,292 | A/C | — | uncertain significance |
| rs777081250 | 12:123,082,325 | C/T | — | uncertain significance |
| rs201757501 | 12:123,082,387 | C/T | — | uncertain significance |
| rs1312190763 | 12:123,086,106 | G/T | — | uncertain significance |
| rs779178448 | 12:123,087,164 | C/A | — | uncertain significance |
| rs371479973 | 12:123,087,167 | G/A | — | uncertain significance |
| rs2547482864 | 12:123,087,189 | T/A | — | uncertain significance |
| rs2547483367 | 12:123,087,414 | T/A | — | uncertain significance |
| rs1271079700 | 12:123,087,574 | T/A | — | uncertain significance |
| rs370507743 | 12:123,087,612 | C/T | — | likely benign |
| rs371016706 | 12:123,087,637 | A/G | — | uncertain significance |
| rs374127774 | 12:123,087,711 | C/G | — | uncertain significance |
| rs750218882 | 12:123,089,125 | T/C | — | uncertain significance |
| rs778179972 | 12:123,089,171 | A/C | — | uncertain significance |
| rs1231728317 | 12:123,089,598 | C/G | — | uncertain significance |
| rs2277346 | 12:123,094,720 | G/A | — | — |
| rs367873698 | 12:123,095,392 | G/A | — | uncertain significance |
| rs1873366239 | 12:123,097,690 | A/G | — | uncertain significance |
| rs185213045 | 12:123,097,699 | G/A | — | uncertain significance |
| rs753836417 | 12:123,097,742 | A/G | — | uncertain significance |
| rs376634701 | 12:123,099,587 | T/C | — | uncertain significance |
| rs6489157 | 12:123,101,673 | G/T | — | — |
| rs528094170 | 12:123,103,091 | G/A | — | uncertain significance |
| rs560306260 | 12:123,105,054 | A/T | — | uncertain significance |
| rs368756882 | 12:123,105,135 | A/G | — | uncertain significance |
| rs375970712 | 12:123,106,486 | A/G | — | uncertain significance |
| rs2547513740 | 12:123,107,017 | T/C | — | likely benign |
| rs2547513743 | 12:123,107,019 | T/G | — | uncertain significance |
| rs760448774 | 12:123,107,100 | C/T | — | likely benign |
| rs770812752 | 12:123,109,147 | T/C | — | uncertain significance |
| rs2547517306 | 12:123,109,149 | G/A | — | uncertain significance |
| rs1220946589 | 12:123,109,188 | T/C | — | uncertain significance |
| rs772156434 | 12:123,110,771 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.