CCAR2
cell cycle and apoptosis regulator 2
Summary
Enables RNA polymerase II complex binding activity and enzyme inhibitor activity. Involved in several processes, including mitochondrial fragmentation involved in apoptotic process; regulation of primary metabolic process; and regulation of signal transduction. Located in several cellular components, including mitochondrial matrix; nucleoplasm; and spindle. Part of DBIRD complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants85 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150400388 | 8:22,463,319 | G/A | — | likely benign |
| rs7843828 | 8:22,463,623 | C/T | — | benign |
| rs148886727 | 8:22,463,657 | A/C | — | uncertain significance |
| rs2291230 | 8:22,463,697 | C/G | — | benign |
| rs2487898197 | 8:22,464,139 | T/C | — | uncertain significance |
| rs147457641 | 8:22,465,513 | T/G | — | likely benign |
| rs754983948 | 8:22,465,517 | C/G | — | uncertain significance |
| rs376168583 | 8:22,465,544 | C/T | — | uncertain significance |
| rs200084191 | 8:22,470,538 | A/C | — | uncertain significance |
| rs138079032 | 8:22,470,585 | G/T | — | uncertain significance |
| rs202200459 | 8:22,471,701 | C/G | — | uncertain significance |
| rs147153683 | 8:22,471,702 | C/A | — | uncertain significance |
| rs367702105 | 8:22,471,721 | C/A | — | uncertain significance |
| rs78169940 | 8:22,471,776 | C/T | — | likely benign |
| rs1801409200 | 8:22,471,808 | A/G | — | uncertain significance |
| rs3736147 | 8:22,471,824 | G/A | — | benign |
| rs145783124 | 8:22,471,983 | G/A | — | likely benign |
| rs752938636 | 8:22,471,989 | G/A | — | likely benign |
| rs759663422 | 8:22,472,369 | G/C | — | uncertain significance |
| rs200083666 | 8:22,472,371 | A/G | — | likely benign |
| rs1246249006 | 8:22,472,425 | C/T | — | likely benign |
| rs112997942 | 8:22,472,473 | G/A | — | benign |
| rs201473135 | 8:22,472,507 | A/T | — | uncertain significance |
| rs147002132 | 8:22,472,512 | G/A | — | likely benign |
| rs7001453 | 8:22,472,950 | C/T | — | benign |
| rs145928227 | 8:22,472,967 | A/T | — | uncertain significance |
| rs200285926 | 8:22,472,984 | C/T | — | uncertain significance |
| rs149267963 | 8:22,472,985 | G/A | — | likely benign |
| rs775175182 | 8:22,473,035 | A/G | — | uncertain significance |
| rs201897291 | 8:22,473,071 | G/C | — | uncertain significance |
| rs143064291 | 8:22,473,078 | A/G | — | uncertain significance |
| rs372863532 | 8:22,473,199 | C/T | — | likely benign |
| rs147092133 | 8:22,473,222 | G/T | — | benign |
| rs6558165 | 8:22,473,224 | T/C | — | benign |
| rs1246673213 | 8:22,473,225 | G/A | — | uncertain significance |
| rs529600420 | 8:22,473,250 | C/T | — | uncertain significance |
| rs1005631499 | 8:22,473,283 | C/A | — | uncertain significance |
| rs377024071 | 8:22,473,295 | C/T | — | likely benign |
| rs138444882 | 8:22,473,296 | G/A | — | likely benign |
| rs1364694653 | 8:22,473,325 | C/T | — | uncertain significance |
| rs150000557 | 8:22,473,327 | C/A | — | uncertain significance |
| rs143313961 | 8:22,473,347 | C/T | — | likely benign |
| rs201363003 | 8:22,473,352 | G/A | — | uncertain significance |
| rs7843128 | 8:22,473,465 | T/G | coding sequence variant | — |
| rs7838922 | 8:22,473,520 | A/G | — | benign |
| rs1420333951 | 8:22,473,589 | A/G | — | uncertain significance |
| rs201261640 | 8:22,473,618 | G/A | — | uncertain significance |
| rs200426159 | 8:22,473,639 | A/G | — | uncertain significance |
| rs143150726 | 8:22,473,646 | A/C | — | likely benign |
| rs148238305 | 8:22,473,648 | G/A | — | uncertain significance |
| rs141217161 | 8:22,473,650 | G/A | — | likely benign |
| rs1801500041 | 8:22,473,691 | A/G | — | uncertain significance |
| rs898292687 | 8:22,473,697 | T/A | — | uncertain significance |
| rs59511580 | 8:22,473,725 | G/C | — | benign |
| rs201457211 | 8:22,473,732 | G/A | — | uncertain significance |
| rs142397736 | 8:22,473,736 | C/T | — | uncertain significance |
| rs141429680 | 8:22,473,737 | G/A | — | benign |
| rs201747747 | 8:22,473,764 | G/A | — | likely benign |
| rs1801570882 | 8:22,474,989 | A/C | — | uncertain significance |
| rs145612413 | 8:22,474,998 | C/T | — | benign |
| rs751680 | 8:22,475,627 | G/T | — | — |
| rs73672800 | 8:22,475,854 | C/T | — | benign |
| rs772718225 | 8:22,475,992 | G/A | — | uncertain significance |
| rs1314907302 | 8:22,475,997 | A/T | — | uncertain significance |
| rs2487973653 | 8:22,476,000 | G/A | — | uncertain significance |
| rs200172196 | 8:22,476,225 | C/T | — | likely benign |
| rs1316427296 | 8:22,476,355 | T/C | — | uncertain significance |
| rs150629840 | 8:22,476,360 | C/G | — | conflicting classifications of pathogenicity |
| rs144664542 | 8:22,476,380 | G/A | — | likely benign |
| rs200099711 | 8:22,476,385 | G/T | — | uncertain significance |
| rs17855313 | 8:22,476,389 | T/C | — | benign |
| rs771314758 | 8:22,476,424 | A/G | — | uncertain significance |
| rs189318060 | 8:22,476,464 | G/A | — | benign |
| rs1230665270 | 8:22,476,516 | G/C | — | uncertain significance |
| rs763636347 | 8:22,476,660 | C/T | — | likely benign |
| rs148866061 | 8:22,476,682 | C/T | — | likely benign |
| rs768872966 | 8:22,476,714 | C/T | — | uncertain significance |
| rs1486677501 | 8:22,476,737 | G/A | — | uncertain significance |
| rs201420827 | 8:22,476,767 | C/T | — | uncertain significance |
| rs769836001 | 8:22,476,774 | C/T | — | uncertain significance |
| rs776186494 | 8:22,476,794 | C/T | — | uncertain significance |
| rs200827249 | 8:22,476,855 | G/A | — | uncertain significance |
| rs568228240 | 8:22,477,163 | G/A | — | uncertain significance |
| rs202120717 | 8:22,477,169 | A/G | — | uncertain significance |
| rs144622807 | 8:22,477,179 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.