ANO8
anoctamin 8
Summary
Enables intracellularly calcium-gated chloride channel activity. Involved in chloride transmembrane transport. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants85 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs77331626 | 19:17,434,093 | T/A | — | — |
| rs781546048 | 19:17,434,340 | T/C | — | uncertain significance |
| rs1001737667 | 19:17,434,349 | A/G | — | uncertain significance |
| rs2513179366 | 19:17,434,405 | T/C | — | uncertain significance |
| rs1368792270 | 19:17,434,467 | C/G | — | uncertain significance |
| rs1191782460 | 19:17,434,484 | G/C | — | uncertain significance |
| rs2513179542 | 19:17,434,516 | G/T | — | uncertain significance |
| rs1205812653 | 19:17,434,517 | C/T | — | uncertain significance |
| rs1322739884 | 19:17,434,526 | C/T | — | uncertain significance |
| rs2074254044 | 19:17,434,553 | C/T | — | uncertain significance |
| rs2513179647 | 19:17,434,564 | G/A | — | uncertain significance |
| rs1395837828 | 19:17,434,594 | G/A | — | uncertain significance |
| rs2513179756 | 19:17,434,604 | G/T | — | uncertain significance |
| rs2074254936 | 19:17,434,627 | G/A | — | uncertain significance |
| rs1362868230 | 19:17,434,669 | G/A | — | uncertain significance |
| rs1419870692 | 19:17,434,670 | C/T | — | uncertain significance |
| rs2513179966 | 19:17,434,679 | G/A | — | uncertain significance |
| rs1263139325 | 19:17,434,693 | C/T | — | uncertain significance |
| rs2074261394 | 19:17,435,538 | C/T | — | uncertain significance |
| rs199523416 | 19:17,435,547 | G/A | — | uncertain significance |
| rs779900024 | 19:17,435,562 | C/T | — | uncertain significance |
| rs772805855 | 19:17,435,585 | G/A | — | uncertain significance |
| rs2513181159 | 19:17,435,601 | C/G | — | uncertain significance |
| rs754345088 | 19:17,435,604 | G/A | — | uncertain significance |
| rs150818557 | 19:17,435,647 | G/A | — | likely benign |
| rs778843591 | 19:17,435,735 | C/T | — | uncertain significance |
| rs761873573 | 19:17,436,012 | T/C | — | uncertain significance |
| rs746119038 | 19:17,436,077 | C/T | — | uncertain significance |
| rs374557842 | 19:17,436,098 | C/T | — | uncertain significance |
| rs1293469887 | 19:17,436,099 | G/A | — | uncertain significance |
| rs753044361 | 19:17,436,122 | C/T | — | uncertain significance |
| rs771912275 | 19:17,436,152 | C/G | — | uncertain significance |
| rs578235436 | 19:17,436,170 | C/T | — | uncertain significance |
| rs1047043926 | 19:17,438,072 | A/T | — | uncertain significance |
| rs899931873 | 19:17,438,109 | C/T | — | uncertain significance |
| rs753940125 | 19:17,438,267 | C/G | — | uncertain significance |
| rs2513184418 | 19:17,438,511 | A/T | — | uncertain significance |
| rs751787050 | 19:17,438,592 | T/C | — | uncertain significance |
| rs148270839 | 19:17,438,677 | C/T | — | uncertain significance |
| rs139815862 | 19:17,439,033 | C/T | — | uncertain significance |
| rs3745191 | 19:17,439,034 | C/T | synonymous variant | — |
| rs765945952 | 19:17,439,156 | G/A | — | uncertain significance |
| rs2513185888 | 19:17,439,206 | T/C | — | uncertain significance |
| rs770449557 | 19:17,439,234 | T/C | — | uncertain significance |
| rs1384911693 | 19:17,439,255 | C/G | — | uncertain significance |
| rs1358288295 | 19:17,439,285 | C/T | — | uncertain significance |
| rs1466079385 | 19:17,439,301 | G/C | — | uncertain significance |
| rs1418517634 | 19:17,439,366 | C/G | — | uncertain significance |
| rs558737027 | 19:17,439,368 | C/A | — | uncertain significance |
| rs956000085 | 19:17,439,369 | A/T | — | uncertain significance |
| rs113297737 | 19:17,439,400 | C/G | — | uncertain significance |
| rs1228912722 | 19:17,439,411 | C/G | — | uncertain significance |
| rs1903561923 | 19:17,439,431 | T/C | — | uncertain significance |
| rs574145559 | 19:17,439,486 | C/T | — | uncertain significance |
| rs1192090122 | 19:17,439,503 | C/T | — | uncertain significance |
| rs974733468 | 19:17,439,594 | C/G | — | uncertain significance |
| rs921936812 | 19:17,439,618 | C/T | — | uncertain significance |
| rs933582687 | 19:17,439,624 | G/A | — | uncertain significance |
| rs959204461 | 19:17,439,662 | A/T | — | uncertain significance |
| rs1229024991 | 19:17,439,700 | C/G | — | uncertain significance |
| rs563077699 | 19:17,439,750 | C/T | — | uncertain significance |
| rs2513187333 | 19:17,439,755 | T/C | — | uncertain significance |
| rs755495019 | 19:17,441,059 | T/A | — | uncertain significance |
| rs1335164709 | 19:17,441,248 | C/A | — | likely benign |
| rs2074308894 | 19:17,441,265 | G/A | — | uncertain significance |
| rs45445097 | 19:17,441,660 | C/T | — | uncertain significance |
| rs2074312837 | 19:17,441,693 | A/G | — | uncertain significance |
| rs539903938 | 19:17,441,792 | G/A | — | uncertain significance |
| rs141250802 | 19:17,441,955 | G/A | — | uncertain significance |
| rs368734165 | 19:17,441,992 | C/A | — | uncertain significance |
| rs776760141 | 19:17,442,128 | C/T | — | uncertain significance |
| rs2513191288 | 19:17,442,161 | T/C | — | uncertain significance |
| rs751946976 | 19:17,442,163 | C/T | — | uncertain significance |
| rs780130844 | 19:17,442,181 | A/G | — | uncertain significance |
| rs886235142 | 19:17,443,804 | T/C | — | uncertain significance |
| rs746597195 | 19:17,444,017 | G/A | — | uncertain significance |
| rs2513194138 | 19:17,444,334 | G/T | — | uncertain significance |
| rs2513194636 | 19:17,444,557 | G/T | — | uncertain significance |
| rs923087661 | 19:17,444,571 | A/G | — | uncertain significance |
| rs200300681 | 19:17,444,573 | C/G | — | uncertain significance |
| rs1449764030 | 19:17,445,391 | G/A | — | uncertain significance |
| rs775046789 | 19:17,445,394 | G/A | — | uncertain significance |
| rs913802425 | 19:17,445,412 | G/A | — | uncertain significance |
| rs750502996 | 19:17,445,434 | C/T | — | uncertain significance |
| rs909649616 | 19:17,445,467 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.