CAND2
cullin associated and neddylation dissociated 2 (putative)
Summary
Predicted to enable TBP-class protein binding activity. Predicted to be involved in SCF complex assembly; positive regulation of DNA-templated transcription; and protein ubiquitination. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants105 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7650482 | 3:12,841,804 | A/G | intron variant | — |
| rs4642101 | 3:12,842,223 | T/G | intron variant | — |
| rs9820977 | 3:12,842,932 | G/A | intron variant | — |
| rs3889514 | 3:12,844,072 | T/C | intron variant | — |
| rs753697377 | 3:12,845,044 | C/A | — | uncertain significance |
| rs9836128 | 3:12,845,426 | G/C | intron variant | — |
| rs745574996 | 3:12,848,813 | C/T | — | uncertain significance |
| rs187232301 | 3:12,848,861 | C/T | — | uncertain significance |
| rs1191430885 | 3:12,848,911 | G/A | — | uncertain significance |
| rs1265025340 | 3:12,848,947 | C/G | — | uncertain significance |
| rs140295185 | 3:12,851,709 | G/A | — | likely benign |
| rs2470929633 | 3:12,851,797 | T/G | — | uncertain significance |
| rs2061841634 | 3:12,851,820 | C/G | — | uncertain significance |
| rs9870433 | 3:12,853,566 | T/C | intron variant | — |
| rs2061870066 | 3:12,854,834 | G/A | — | uncertain significance |
| rs138783925 | 3:12,854,873 | A/T | — | likely benign |
| rs147325718 | 3:12,856,664 | A/G | — | uncertain significance |
| rs376394990 | 3:12,856,669 | G/A | — | uncertain significance |
| rs1249805909 | 3:12,856,708 | A/G | — | uncertain significance |
| rs61737053 | 3:12,856,727 | C/T | — | uncertain significance |
| rs750521408 | 3:12,856,747 | G/A | — | uncertain significance |
| rs367649451 | 3:12,856,771 | G/C | — | uncertain significance |
| rs1197680108 | 3:12,856,781 | G/A | — | uncertain significance |
| rs752676710 | 3:12,856,837 | G/A | — | uncertain significance |
| rs2061889875 | 3:12,856,880 | C/T | — | uncertain significance |
| rs769635010 | 3:12,856,928 | G/A | — | uncertain significance |
| rs753774394 | 3:12,857,393 | C/T | — | uncertain significance |
| rs201739910 | 3:12,857,408 | C/T | — | uncertain significance |
| rs200578477 | 3:12,857,413 | C/G | — | uncertain significance |
| rs373749682 | 3:12,857,414 | G/A | — | likely benign |
| rs574811386 | 3:12,857,424 | G/T | — | uncertain significance |
| rs775069513 | 3:12,857,460 | G/A | — | uncertain significance |
| rs1290513545 | 3:12,857,505 | C/T | — | uncertain significance |
| rs1412224481 | 3:12,857,881 | T/A | — | uncertain significance |
| rs1185561299 | 3:12,857,900 | C/G | — | uncertain significance |
| rs62637643 | 3:12,857,904 | C/T | — | benign |
| rs201773087 | 3:12,857,959 | G/A | — | uncertain significance |
| rs760936753 | 3:12,858,049 | G/A | — | uncertain significance |
| rs377274058 | 3:12,858,080 | G/A | — | likely benign |
| rs369765807 | 3:12,858,092 | C/T | — | uncertain significance |
| rs373922459 | 3:12,858,101 | G/A | — | uncertain significance |
| rs574738317 | 3:12,858,106 | C/T | — | uncertain significance |
| rs1392836335 | 3:12,858,199 | C/T | — | uncertain significance |
| rs766844513 | 3:12,858,265 | C/T | — | uncertain significance |
| rs371066830 | 3:12,858,269 | C/T | — | uncertain significance |
| rs780125791 | 3:12,858,296 | G/A | — | uncertain significance |
| rs754877644 | 3:12,858,310 | C/T | — | uncertain significance |
| rs186305305 | 3:12,858,319 | G/A | — | uncertain significance |
| rs199996088 | 3:12,858,346 | G/A | — | uncertain significance |
| rs201105764 | 3:12,858,380 | T/A | — | uncertain significance |
| rs761087384 | 3:12,858,409 | T/A | — | uncertain significance |
| rs767487548 | 3:12,858,437 | G/A | — | uncertain significance |
| rs996762339 | 3:12,858,446 | C/T | — | uncertain significance |
| rs2470942263 | 3:12,858,471 | C/T | — | likely benign |
| rs2470942272 | 3:12,858,474 | G/C | — | uncertain significance |
| rs1000519062 | 3:12,858,476 | G/A | — | uncertain significance |
| rs201904182 | 3:12,858,543 | C/T | — | likely benign |
| rs180768267 | 3:12,858,557 | A/G | — | benign |
| rs577324477 | 3:12,858,575 | T/C | — | uncertain significance |
| rs984749634 | 3:12,858,595 | A/G | — | uncertain significance |
| rs539921240 | 3:12,858,655 | C/T | — | uncertain significance |
| rs765251148 | 3:12,858,707 | G/C | — | uncertain significance |
| rs191368596 | 3:12,858,733 | C/T | — | uncertain significance |
| rs2470943027 | 3:12,858,754 | G/T | — | uncertain significance |
| rs200492486 | 3:12,858,779 | C/T | — | uncertain significance |
| rs201715663 | 3:12,858,847 | C/T | — | uncertain significance |
| rs551851915 | 3:12,858,848 | G/A | — | uncertain significance |
| rs764506700 | 3:12,858,860 | C/T | — | uncertain significance |
| rs944391991 | 3:12,858,863 | T/C | — | uncertain significance |
| rs747643034 | 3:12,858,905 | G/A | — | uncertain significance |
| rs377395230 | 3:12,858,916 | G/A | — | uncertain significance |
| rs1289218637 | 3:12,858,946 | G/C | — | uncertain significance |
| rs373807883 | 3:12,859,082 | C/T | — | uncertain significance |
| rs199720424 | 3:12,859,091 | G/A | — | uncertain significance |
| rs746821713 | 3:12,859,099 | G/A | — | uncertain significance |
| rs774791381 | 3:12,859,204 | G/A | — | uncertain significance |
| rs188658460 | 3:12,859,262 | G/T | — | uncertain significance |
| rs2470944647 | 3:12,859,273 | G/A | — | uncertain significance |
| rs761170457 | 3:12,859,289 | G/A | — | uncertain significance |
| rs191057169 | 3:12,859,324 | C/G | — | uncertain significance |
| rs201658408 | 3:12,859,342 | C/T | — | uncertain significance |
| rs748841467 | 3:12,859,352 | G/A | — | uncertain significance |
| rs181307051 | 3:12,861,600 | G/A | — | benign |
| rs145134860 | 3:12,861,637 | G/A | — | likely benign |
| rs2470949258 | 3:12,861,642 | A/G | — | uncertain significance |
| rs139572691 | 3:12,867,010 | C/T | — | benign |
| rs536119459 | 3:12,867,011 | G/T | — | uncertain significance |
| rs767124122 | 3:12,867,067 | C/T | — | uncertain significance |
| rs2470005759 | 3:12,867,091 | C/T | — | uncertain significance |
| rs77920251 | 3:12,867,121 | C/T | — | uncertain significance |
| rs762266814 | 3:12,867,127 | C/A | — | uncertain significance |
| rs779676513 | 3:12,868,984 | G/A | — | uncertain significance |
| rs201022461 | 3:12,869,045 | A/G | — | uncertain significance |
| rs777671212 | 3:12,869,086 | G/A | — | uncertain significance |
| rs746327955 | 3:12,872,967 | C/G | — | uncertain significance |
| rs75387493 | 3:12,872,995 | C/T | — | benign |
| rs200780693 | 3:12,873,040 | T/C | — | uncertain significance |
| rs2062075025 | 3:12,875,295 | T/G | — | uncertain significance |
| rs768520399 | 3:12,875,305 | C/T | — | uncertain significance |
| rs200379985 | 3:12,875,306 | G/A | — | uncertain significance |
Showing 100 of 105 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.