OR4C46
olfactory receptor family 4 subfamily C member 46
Summary
Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139375426 | 11:51,515,286 | A/G | — | uncertain significance |
| rs757308478 | 11:51,515,297 | A/T | — | uncertain significance |
| rs372066510 | 11:51,515,344 | G/T | — | uncertain significance |
| rs537148411 | 11:51,515,396 | G/A | — | uncertain significance |
| rs1266168332 | 11:51,515,418 | C/G | — | uncertain significance |
| rs777103481 | 11:51,515,466 | C/T | — | uncertain significance |
| rs770437587 | 11:51,515,469 | A/G | — | uncertain significance |
| rs199500599 | 11:51,515,481 | T/A | — | uncertain significance |
| rs765805591 | 11:51,515,483 | G/A | — | uncertain significance |
| rs1369935243 | 11:51,515,499 | C/A | — | uncertain significance |
| rs372260777 | 11:51,515,519 | A/T | — | uncertain significance |
| rs149453010 | 11:51,515,520 | T/C | — | uncertain significance |
| rs759711172 | 11:51,515,531 | C/T | — | uncertain significance |
| rs1261552731 | 11:51,515,540 | A/C | — | uncertain significance |
| rs144006817 | 11:51,515,547 | C/T | — | uncertain significance |
| rs141105102 | 11:51,515,604 | C/T | — | likely benign |
| rs760902808 | 11:51,515,638 | C/A | — | uncertain significance |
| rs74396937 | 11:51,515,640 | A/G | — | benign |
| rs140059362 | 11:51,515,648 | G/A | — | uncertain significance |
| rs369188875 | 11:51,515,652 | T/A | — | uncertain significance |
| rs146712655 | 11:51,515,666 | C/T | — | uncertain significance |
| rs140334906 | 11:51,515,672 | A/G | — | uncertain significance |
| rs769688875 | 11:51,515,675 | A/T | — | uncertain significance |
| rs1428805366 | 11:51,515,691 | G/A | — | uncertain significance |
| rs370667433 | 11:51,515,720 | T/G | — | uncertain significance |
| rs1435239003 | 11:51,515,724 | T/A | — | uncertain significance |
| rs138732849 | 11:51,515,727 | G/T | — | uncertain significance |
| rs374443791 | 11:51,515,749 | A/G | — | uncertain significance |
| rs1862992361 | 11:51,515,810 | T/G | — | uncertain significance |
| rs543950860 | 11:51,515,837 | G/A | — | uncertain significance |
| rs757359554 | 11:51,515,850 | C/T | — | uncertain significance |
| rs779865482 | 11:51,515,852 | C/T | — | uncertain significance |
| rs111836905 | 11:51,515,856 | T/A | — | uncertain significance |
| rs768609619 | 11:51,515,862 | A/G | — | likely benign |
| rs143736787 | 11:51,515,874 | C/T | — | uncertain significance |
| rs77689730 | 11:51,515,912 | C/A | missense variant | — |
| rs188287779 | 11:51,515,943 | G/T | — | uncertain significance |
| rs751837741 | 11:51,515,946 | C/A | — | uncertain significance |
| rs140563000 | 11:51,516,025 | C/G | — | uncertain significance |
| rs150447323 | 11:51,516,029 | G/T | — | uncertain significance |
| rs764793859 | 11:51,516,038 | A/G | — | uncertain significance |
| rs756402712 | 11:51,516,057 | C/A | — | uncertain significance |
| rs138830098 | 11:51,516,090 | C/T | — | uncertain significance |
| rs1862982900 | 11:51,516,101 | A/G | — | uncertain significance |
| rs751149656 | 11:51,516,119 | T/G | — | uncertain significance |
| rs754680740 | 11:51,516,125 | C/T | — | uncertain significance |
| rs779380858 | 11:51,516,135 | A/G | — | uncertain significance |
| rs11246609 | 11:51,516,144 | A/G | — | benign |
| rs548492164 | 11:51,516,145 | G/T | — | uncertain significance |
| rs139582967 | 11:51,516,150 | C/T | — | uncertain significance |
| rs762996578 | 11:51,516,165 | C/T | — | uncertain significance |
| rs140000110 | 11:51,516,191 | G/A | — | likely benign |
| rs1464584151 | 11:51,516,200 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.