BCAN
brevican
Summary
This gene encodes a member of the lectican family of chondroitin sulfate proteoglycans that is specifically expressed in the central nervous system. This protein is developmentally regulated and may function in the formation of the brain extracellular matrix. This protein is highly expressed in gliomas and may promote the growth and cell motility of brain tumor cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011]
Known Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs113184515 | 1:156,613,674 | G/C | coding sequence variant | — |
| rs553607798 | 1:156,615,917 | T/C | — | likely benign |
| rs376527030 | 1:156,616,757 | C/T | — | uncertain significance |
| rs770872561 | 1:156,616,785 | G/A | — | uncertain significance |
| rs138687652 | 1:156,616,791 | G/A | — | uncertain significance |
| rs2524805481 | 1:156,616,805 | G/C | — | uncertain significance |
| rs115373136 | 1:156,616,814 | C/G | — | benign |
| rs770066543 | 1:156,616,886 | C/T | — | uncertain significance |
| rs2524806145 | 1:156,616,911 | G/T | — | uncertain significance |
| rs376404213 | 1:156,616,925 | G/A | — | uncertain significance |
| rs200321248 | 1:156,617,330 | C/T | — | uncertain significance |
| rs148799690 | 1:156,617,333 | G/A | — | uncertain significance |
| rs1479296371 | 1:156,617,338 | G/A | — | uncertain significance |
| rs558655305 | 1:156,617,858 | C/T | — | uncertain significance |
| rs2524820309 | 1:156,621,254 | C/T | — | uncertain significance |
| rs2524820363 | 1:156,621,265 | G/A | — | uncertain significance |
| rs1301027329 | 1:156,621,307 | G/C | — | uncertain significance |
| rs767405069 | 1:156,621,335 | C/G | — | uncertain significance |
| rs369041752 | 1:156,621,388 | C/T | — | uncertain significance |
| rs373345126 | 1:156,621,389 | G/A | — | uncertain significance |
| rs147658469 | 1:156,621,437 | G/A | — | uncertain significance |
| rs2524821280 | 1:156,621,442 | A/G | — | uncertain significance |
| rs2524824047 | 1:156,622,119 | T/C | — | likely benign |
| rs754820500 | 1:156,622,195 | G/A | — | uncertain significance |
| rs377653408 | 1:156,622,198 | C/T | — | likely benign |
| rs1483533272 | 1:156,622,205 | G/C | — | uncertain significance |
| rs141542995 | 1:156,622,208 | C/T | — | likely benign |
| rs765643575 | 1:156,622,232 | C/G | — | uncertain significance |
| rs139064894 | 1:156,622,287 | G/A | — | likely benign |
| rs760147033 | 1:156,622,439 | G/A | — | uncertain significance |
| rs143807661 | 1:156,622,453 | G/A | — | uncertain significance |
| rs755206465 | 1:156,622,474 | C/T | — | uncertain significance |
| rs151184855 | 1:156,622,495 | A/G | — | uncertain significance |
| rs537017904 | 1:156,622,507 | G/A | — | uncertain significance |
| rs763602865 | 1:156,622,513 | G/A | — | uncertain significance |
| rs374149344 | 1:156,622,520 | C/T | — | uncertain significance |
| rs62001922 | 1:156,622,525 | A/C | — | benign |
| rs750438354 | 1:156,622,537 | C/T | — | uncertain significance |
| rs761504175 | 1:156,622,538 | G/A | — | uncertain significance |
| rs148943492 | 1:156,622,669 | G/A | — | uncertain significance |
| rs548144047 | 1:156,626,084 | C/T | — | benign |
| rs775100384 | 1:156,626,136 | C/T | — | uncertain significance |
| rs138466651 | 1:156,626,137 | G/A | — | uncertain significance |
| rs201179524 | 1:156,626,166 | G/C | — | uncertain significance |
| rs41267397 | 1:156,626,796 | G/T | — | likely benign |
| rs1161484405 | 1:156,626,858 | A/C | — | uncertain significance |
| rs751771805 | 1:156,627,502 | G/A | — | uncertain significance |
| rs371785076 | 1:156,627,505 | A/G | — | uncertain significance |
| rs765702318 | 1:156,627,986 | T/C | — | uncertain significance |
| rs762033515 | 1:156,628,347 | C/T | — | uncertain significance |
| rs376073829 | 1:156,628,353 | C/T | — | uncertain significance |
| rs373863041 | 1:156,628,379 | G/A | — | uncertain significance |
| rs568359750 | 1:156,628,386 | C/G | — | uncertain significance |
| rs377028062 | 1:156,628,395 | G/A | — | uncertain significance |
| rs144692174 | 1:156,628,412 | G/C | — | uncertain significance |
| rs200282065 | 1:156,628,415 | C/T | — | uncertain significance |
| rs761090540 | 1:156,628,475 | G/A | — | uncertain significance |
| rs761374302 | 1:156,628,491 | A/G | — | uncertain significance |
| rs539632414 | 1:156,628,524 | C/G | — | uncertain significance |
| rs1477237282 | 1:156,628,833 | C/A | — | uncertain significance |
| rs149321570 | 1:156,628,877 | G/A | — | likely benign |
| rs202001625 | 1:156,628,885 | G/A | — | likely benign |
| rs267598078 | 1:156,628,904 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.