CCDC85A
coiled-coil domain containing 85A
Summary
Located in adherens junction. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs917672547 | 2:56,411,764 | C/G | — | uncertain significance |
| rs573551108 | 2:56,411,797 | C/T | — | uncertain significance |
| rs758574817 | 2:56,411,806 | A/G | — | uncertain significance |
| rs1276281281 | 2:56,411,820 | G/T | — | uncertain significance |
| rs1348346140 | 2:56,411,821 | C/T | — | uncertain significance |
| rs1047552361 | 2:56,411,833 | C/G | — | uncertain significance |
| rs952714241 | 2:56,411,885 | G/C | — | uncertain significance |
| rs760317264 | 2:56,411,919 | C/T | — | uncertain significance |
| rs2465896575 | 2:56,419,622 | A/T | — | uncertain significance |
| rs1165642262 | 2:56,419,723 | G/A | — | uncertain significance |
| rs768459730 | 2:56,419,729 | T/C | — | uncertain significance |
| rs1225684148 | 2:56,419,759 | G/T | — | uncertain significance |
| rs377020827 | 2:56,419,909 | A/G | — | uncertain significance |
| rs1285110339 | 2:56,419,921 | C/G | — | uncertain significance |
| rs759751798 | 2:56,419,936 | G/C | — | uncertain significance |
| rs1052182749 | 2:56,420,036 | C/T | — | uncertain significance |
| rs374744627 | 2:56,420,103 | C/T | — | likely benign |
| rs762250399 | 2:56,420,104 | G/A | — | uncertain significance |
| rs1676363980 | 2:56,420,108 | A/G | — | uncertain significance |
| rs763634368 | 2:56,420,146 | C/A | — | uncertain significance |
| rs2465899130 | 2:56,420,158 | A/G | — | uncertain significance |
| rs1157673701 | 2:56,420,203 | C/T | — | uncertain significance |
| rs1045637334 | 2:56,420,255 | A/T | — | uncertain significance |
| rs369035576 | 2:56,420,324 | G/C | — | uncertain significance |
| rs752911674 | 2:56,420,327 | A/G | — | uncertain significance |
| rs201081645 | 2:56,420,329 | A/G | — | uncertain significance |
| rs772737505 | 2:56,420,368 | G/T | — | uncertain significance |
| rs200423664 | 2:56,420,369 | G/C | — | uncertain significance |
| rs139777024 | 2:56,420,484 | C/A | — | likely benign |
| rs368722854 | 2:56,420,557 | G/A | — | uncertain significance |
| rs114819003 | 2:56,552,246 | G/A | intron variant | — |
| rs376064938 | 2:56,570,047 | C/T | — | uncertain significance |
| rs371781745 | 2:56,570,077 | G/T | — | uncertain significance |
| rs6545572 | 2:56,581,563 | C/T | intron variant | — |
| rs17268785 | 2:56,592,083 | A/T | — | — |
| rs374131041 | 2:56,599,534 | G/A | — | uncertain significance |
| rs751452419 | 2:56,599,588 | T/C | — | uncertain significance |
| rs780223971 | 2:56,602,951 | G/C | — | uncertain significance |
| rs1352778935 | 2:56,603,011 | A/G | — | uncertain significance |
| rs757976295 | 2:56,611,485 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.