DOCK10
dedicator of cytokinesis 10
Summary
This gene encodes a member of the dedicator of cytokinesis protein family. Members of this family are guanosine nucleotide exchange factors for Rho GTPases and defined by the presence of conserved DOCK-homology regions. The encoded protein belongs to the D (or Zizimin) subfamily of DOCK proteins, which also contain an N-terminal pleckstrin homology domain. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Mar 2014]
Known Variants125 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs368600276 | 2:225,630,481 | G/A | — | uncertain significance |
| rs1284260880 | 2:225,630,497 | T/C | — | uncertain significance |
| rs2469400041 | 2:225,630,548 | C/A | — | likely benign |
| rs2469441996 | 2:225,634,939 | T/C | — | uncertain significance |
| rs1019957508 | 2:225,634,944 | G/A | — | uncertain significance |
| rs200577403 | 2:225,634,954 | C/T | — | uncertain significance |
| rs1458619542 | 2:225,635,050 | A/C | — | uncertain significance |
| rs550441284 | 2:225,635,053 | C/T | — | uncertain significance |
| rs201549682 | 2:225,635,275 | T/C | — | uncertain significance |
| rs2469447570 | 2:225,635,331 | G/T | — | uncertain significance |
| rs368336784 | 2:225,635,334 | C/T | — | uncertain significance |
| rs907372379 | 2:225,635,345 | C/T | — | uncertain significance |
| rs16866166 | 2:225,637,976 | G/A | — | benign |
| rs527546362 | 2:225,639,678 | G/A | — | uncertain significance |
| rs370524123 | 2:225,639,709 | G/T | — | uncertain significance |
| rs755681454 | 2:225,639,744 | C/T | — | uncertain significance |
| rs16866167 | 2:225,639,785 | G/A | — | benign |
| rs368630062 | 2:225,639,828 | T/C | — | uncertain significance |
| rs542085964 | 2:225,642,980 | C/T | — | uncertain significance |
| rs746296909 | 2:225,651,843 | C/T | — | uncertain significance |
| rs749062697 | 2:225,653,880 | G/C | — | uncertain significance |
| rs770065045 | 2:225,657,732 | G/C | — | uncertain significance |
| rs775672141 | 2:225,657,733 | G/A | — | uncertain significance |
| rs372066560 | 2:225,658,158 | A/T | — | uncertain significance |
| rs779171619 | 2:225,659,748 | T/A | — | uncertain significance |
| rs1305763186 | 2:225,659,771 | C/T | — | uncertain significance |
| rs374429396 | 2:225,661,056 | C/T | — | uncertain significance |
| rs910558091 | 2:225,661,080 | A/C | — | uncertain significance |
| rs776371353 | 2:225,661,092 | G/A | — | uncertain significance |
| rs201933376 | 2:225,661,704 | A/C | — | uncertain significance |
| rs761132574 | 2:225,661,778 | C/T | — | uncertain significance |
| rs2469733914 | 2:225,662,554 | A/G | — | uncertain significance |
| rs57422537 | 2:225,664,984 | T/C | — | benign |
| rs372043686 | 2:225,666,648 | C/G | — | uncertain significance |
| rs760934070 | 2:225,666,657 | G/T | — | uncertain significance |
| rs778290012 | 2:225,666,731 | C/T | — | uncertain significance |
| rs945112250 | 2:225,669,523 | C/T | — | uncertain significance |
| rs928878330 | 2:225,669,558 | G/T | — | uncertain significance |
| rs756681191 | 2:225,669,827 | A/T | — | uncertain significance |
| rs116790520 | 2:225,669,927 | C/T | — | benign |
| rs371947771 | 2:225,669,944 | T/C | — | uncertain significance |
| rs376223850 | 2:225,669,952 | A/T | — | uncertain significance |
| rs536282568 | 2:225,670,211 | C/T | — | uncertain significance |
| rs375740801 | 2:225,670,845 | G/T | — | uncertain significance |
| rs201934900 | 2:225,670,857 | A/G | — | uncertain significance |
| rs760411967 | 2:225,670,864 | C/G | — | uncertain significance |
| rs2469833408 | 2:225,670,921 | A/G | — | uncertain significance |
| rs765160296 | 2:225,672,399 | T/C | — | uncertain significance |
| rs368187113 | 2:225,672,456 | T/C | — | uncertain significance |
| rs1352667081 | 2:225,672,633 | C/T | — | uncertain significance |
| rs778080607 | 2:225,672,638 | T/A | — | uncertain significance |
| rs367804674 | 2:225,672,641 | C/T | — | uncertain significance |
| rs200998922 | 2:225,672,737 | C/T | — | uncertain significance |
| rs765222025 | 2:225,672,751 | G/C | — | uncertain significance |
| rs1189189381 | 2:225,672,795 | C/T | — | uncertain significance |
| rs542556252 | 2:225,684,177 | A/C | — | uncertain significance |
| rs753305029 | 2:225,684,245 | C/T | — | uncertain significance |
| rs371861682 | 2:225,688,235 | C/T | — | uncertain significance |
| rs57148205 | 2:225,689,421 | G/A | intron variant | — |
| rs199559649 | 2:225,695,293 | T/C | — | uncertain significance |
| rs11681888 | 2:225,696,969 | A/T | regulatory region variant | — |
| rs2470103336 | 2:225,698,964 | C/G | — | likely benign |
| rs369073678 | 2:225,702,538 | C/T | — | uncertain significance |
| rs113378246 | 2:225,706,532 | G/A | — | uncertain significance |
| rs190646257 | 2:225,706,555 | T/G | missense variant | — |
| rs376059455 | 2:225,706,584 | C/G | — | uncertain significance |
| rs534318769 | 2:225,709,555 | T/C | — | uncertain significance |
| rs1401763917 | 2:225,710,266 | C/T | — | uncertain significance |
| rs201110054 | 2:225,710,359 | C/T | — | uncertain significance |
| rs112637383 | 2:225,712,961 | G/A | regulatory region variant | — |
| rs1224130733 | 2:225,714,245 | C/G | — | uncertain significance |
| rs199685603 | 2:225,714,274 | C/T | — | uncertain significance |
| rs765707253 | 2:225,714,289 | G/A | — | uncertain significance |
| rs1402410210 | 2:225,714,300 | G/C | — | uncertain significance |
| rs200712608 | 2:225,714,315 | C/T | — | uncertain significance |
| rs200829813 | 2:225,717,117 | C/T | — | uncertain significance |
| rs2470286732 | 2:225,717,653 | T/G | — | uncertain significance |
| rs369075349 | 2:225,717,688 | T/G | — | uncertain significance |
| rs1322081096 | 2:225,719,694 | G/A | — | uncertain significance |
| rs753950169 | 2:225,721,635 | G/T | — | uncertain significance |
| rs2470407879 | 2:225,729,305 | C/T | — | uncertain significance |
| rs370658203 | 2:225,729,612 | G/C | — | uncertain significance |
| rs2470412750 | 2:225,729,615 | G/A | — | likely benign |
| rs756018663 | 2:225,729,643 | T/A | — | uncertain significance |
| rs1458863210 | 2:225,729,705 | G/T | — | uncertain significance |
| rs2470414260 | 2:225,729,719 | T/C | — | uncertain significance |
| rs765044178 | 2:225,729,774 | A/G | — | uncertain significance |
| rs777425371 | 2:225,738,717 | G/A | — | uncertain significance |
| rs754124482 | 2:225,738,775 | T/C | — | uncertain significance |
| rs374506514 | 2:225,738,835 | G/A | — | uncertain significance |
| rs377019781 | 2:225,739,029 | C/T | — | uncertain significance |
| rs775421344 | 2:225,739,398 | G/T | — | uncertain significance |
| rs2470505019 | 2:225,739,418 | A/C | — | uncertain significance |
| rs147869852 | 2:225,739,435 | G/A | — | uncertain significance |
| rs114242232 | 2:225,739,440 | T/G | — | benign |
| rs761069813 | 2:225,739,447 | G/T | — | uncertain significance |
| rs2470517885 | 2:225,740,757 | A/G | — | uncertain significance |
| rs180691490 | 2:225,740,784 | C/T | — | conflicting classifications of pathogenicity |
| rs771303087 | 2:225,740,827 | G/A | — | uncertain significance |
| rs558377753 | 2:225,740,916 | G/A | — | uncertain significance |
Showing 100 of 125 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.