ADCY1
adenylate cyclase 1
Summary
This gene encodes a member of the of adenylate cyclase gene family that is primarily expressed in the brain. This protein is regulated by calcium/calmodulin concentration and may be involved in brain development. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]
Known Variants257 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1792260445 | 7:45,614,146 | G/C | — | uncertain significance |
| rs1305526913 | 7:45,614,169 | C/A | — | likely benign |
| rs932221184 | 7:45,614,191 | G/A | — | uncertain significance |
| rs1338596701 | 7:45,614,227 | C/T | — | uncertain significance |
| rs1439485446 | 7:45,614,231 | G/C | — | uncertain significance |
| rs760606743 | 7:45,614,242 | C/G | — | uncertain significance |
| rs2483862424 | 7:45,614,284 | C/T | — | likely benign |
| rs1478175668 | 7:45,614,315 | A/G | — | uncertain significance |
| rs531991756 | 7:45,614,346 | C/T | — | likely benign |
| rs544024276 | 7:45,614,359 | G/A | — | uncertain significance |
| rs1266467984 | 7:45,614,373 | G/A | — | likely benign |
| rs74641956 | 7:45,614,376 | C/G | — | benign |
| rs375141353 | 7:45,614,390 | C/T | — | likely benign |
| rs1379522327 | 7:45,614,393 | C/G | — | uncertain significance |
| rs200597993 | 7:45,614,400 | C/G | — | likely benign |
| rs1288537927 | 7:45,614,415 | C/A | — | likely benign |
| rs2483863861 | 7:45,614,420 | G/A | — | uncertain significance |
| rs761931194 | 7:45,614,442 | C/T | — | likely benign |
| rs2483864153 | 7:45,614,479 | T/C | — | uncertain significance |
| rs1314063804 | 7:45,614,492 | C/T | — | uncertain significance |
| rs1210954476 | 7:45,614,493 | C/T | — | likely benign |
| rs1035746347 | 7:45,614,529 | C/A | — | uncertain significance |
| rs2115677876 | 7:45,614,557 | C/T | — | uncertain significance |
| rs746848171 | 7:45,614,565 | G/C | — | likely benign |
| rs1248179913 | 7:45,614,581 | C/G | — | uncertain significance |
| rs761877943 | 7:45,614,582 | G/C | — | uncertain significance |
| rs1562667944 | 7:45,614,592 | C/T | — | uncertain significance |
| rs1441071960 | 7:45,614,597 | C/A | — | uncertain significance |
| rs766548504 | 7:45,614,604 | G/A | — | likely benign |
| rs1053027503 | 7:45,614,606 | G/T | — | uncertain significance |
| rs1163141945 | 7:45,614,611 | G/A | — | uncertain significance |
| rs2483865275 | 7:45,614,617 | G/T | — | uncertain significance |
| rs370830411 | 7:45,614,652 | C/T | — | likely benign |
| rs778441100 | 7:45,614,685 | C/A | — | uncertain significance |
| rs1235710592 | 7:45,614,695 | A/G | — | uncertain significance |
| rs748029352 | 7:45,614,744 | C/T | — | uncertain significance |
| rs2115679315 | 7:45,614,745 | C/T | — | likely benign |
| rs7800818 | 7:45,632,091 | G/A | — | benign |
| rs375794628 | 7:45,632,160 | G/A | — | likely benign |
| rs2115778481 | 7:45,632,355 | C/T | — | uncertain significance |
| rs75774464 | 7:45,632,360 | C/T | — | likely benign |
| rs976166587 | 7:45,632,362 | G/T | — | uncertain significance |
| rs1465089544 | 7:45,632,387 | T/C | — | likely benign |
| rs75000917 | 7:45,632,443 | C/T | — | uncertain significance |
| rs17567824 | 7:45,632,622 | T/G | — | benign |
| rs185529103 | 7:45,649,893 | G/A | — | likely benign |
| rs763452362 | 7:45,649,967 | C/G | — | likely benign |
| rs76595582 | 7:45,649,975 | C/T | — | uncertain significance |
| rs2483962351 | 7:45,649,986 | C/T | — | likely benign |
| rs144232626 | 7:45,650,004 | C/G | — | likely benign |
| rs80190930 | 7:45,650,011 | G/A | — | uncertain significance |
| rs78087585 | 7:45,650,085 | C/T | — | benign |
| rs375484859 | 7:45,650,115 | C/T | — | likely benign |
| rs78742829 | 7:45,650,116 | G/A | — | benign |
| rs149046222 | 7:45,650,372 | G/A | — | benign |
| rs375340972 | 7:45,650,389 | G/A | — | benign |
| rs797005980 | 7:45,650,396 | T/G | — | benign |
| rs191788558 | 7:45,650,398 | G/T | — | benign |
| rs866534633 | 7:45,650,418 | T/A | — | likely benign |
| rs2484003214 | 7:45,662,212 | G/A | — | likely benign |
| rs148862065 | 7:45,662,306 | C/T | — | likely benign |
| rs143472730 | 7:45,662,327 | C/T | — | likely benign |
| rs188916223 | 7:45,662,353 | C/T | — | benign |
| rs36092155 | 7:45,688,073 | A/G | — | benign |
| rs3735672 | 7:45,688,233 | A/G | — | benign |
| rs373262043 | 7:45,688,271 | G/A | — | likely benign |
| rs377495931 | 7:45,688,316 | C/T | — | likely benign |
| rs151091562 | 7:45,688,346 | C/T | — | likely benign |
| rs141023985 | 7:45,688,379 | C/T | — | likely benign |
| rs78870608 | 7:45,688,408 | G/A | — | likely benign |
| rs199602800 | 7:45,688,411 | G/C | — | likely benign |
| rs1195593281 | 7:45,688,414 | C/A | — | likely benign |
| rs6946621 | 7:45,688,575 | G/A | — | benign |
| rs114094515 | 7:45,688,593 | C/T | — | likely benign |
| rs145598308 | 7:45,688,616 | C/T | — | likely benign |
| rs111930963 | 7:45,697,068 | A/T | — | likely benign |
| rs140011019 | 7:45,697,088 | C/T | — | likely benign |
| rs2461131 | 7:45,697,295 | C/G | — | benign |
| rs2471231 | 7:45,697,297 | C/T | — | benign |
| rs557303940 | 7:45,697,306 | G/A | — | likely benign |
| rs767956323 | 7:45,697,344 | C/T | — | likely benign |
| rs1794981677 | 7:45,697,351 | G/A | — | uncertain significance |
| rs369432043 | 7:45,697,377 | C/T | — | likely benign |
| rs139030994 | 7:45,697,380 | G/A | — | likely benign |
| rs746846166 | 7:45,697,386 | G/T | — | uncertain significance |
| rs536487311 | 7:45,697,411 | C/A | — | uncertain significance |
| rs142228376 | 7:45,697,428 | C/T | — | likely benign |
| rs145659731 | 7:45,697,470 | C/T | — | likely benign |
| rs886629273 | 7:45,697,498 | G/A | — | likely benign |
| rs370164101 | 7:45,697,502 | T/G | — | likely benign |
| rs11976730 | 7:45,699,433 | T/C | — | benign |
| rs11973107 | 7:45,699,434 | G/T | — | benign |
| rs2484103727 | 7:45,699,632 | C/T | — | likely benign |
| rs1250488516 | 7:45,699,643 | A/G | — | uncertain significance |
| rs759252700 | 7:45,699,662 | G/A | — | likely benign |
| rs779884375 | 7:45,699,671 | G/A | — | likely benign |
| rs753960227 | 7:45,699,684 | G/C | — | uncertain significance |
| rs1281383000 | 7:45,699,707 | C/T | — | likely benign |
| rs1055365568 | 7:45,699,739 | A/G | — | uncertain significance |
| rs2484104210 | 7:45,699,775 | G/A | — | uncertain significance |
Showing 100 of 257 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.