TMEM116
transmembrane protein 116
Summary
Predicted to be involved in signal transduction. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs192736912 | 12:112,345,925 | A/G | intergenic variant | — |
| rs1225535157 | 12:112,352,746 | T/A | — | — |
| rs75468472 | 12:112,363,239 | T/C | — | — |
| rs1297364356 | 12:112,367,084 | G/A | — | — |
| rs1340910297 | 12:112,367,086 | G/A | — | — |
| rs757556503 | 12:112,369,523 | T/C | — | uncertain significance |
| rs375840968 | 12:112,369,543 | C/T | — | uncertain significance |
| rs368109524 | 12:112,371,696 | C/T | — | uncertain significance |
| rs1389885430 | 12:112,371,780 | A/G | — | uncertain significance |
| rs2072234758 | 12:112,374,970 | C/G | — | uncertain significance |
| rs999390094 | 12:112,375,029 | C/A | — | uncertain significance |
| rs182679952 | 12:112,376,368 | A/C | intron variant | — |
| rs2339905 | 12:112,378,365 | A/G | — | — |
| rs7967238 | 12:112,378,371 | G/A | intron variant | — |
| rs2542723134 | 12:112,381,125 | A/C | — | uncertain significance |
| rs562826268 | 12:112,381,158 | A/G | — | uncertain significance |
| rs76596471 | 12:112,412,518 | T/C | intron variant | — |
| rs2542961860 | 12:112,429,584 | T/C | — | uncertain significance |
| rs757867769 | 12:112,429,601 | A/C | — | uncertain significance |
| rs2542962126 | 12:112,429,638 | A/T | — | uncertain significance |
| rs1298685877 | 12:112,429,642 | A/G | — | uncertain significance |
| rs11066120 | 12:112,436,195 | C/T | downstream gene variant | — |
| rs76181728 | 12:112,437,124 | G/A | regulatory region variant | — |
| rs7306804 | 12:112,441,089 | A/T | — | — |
| rs1049665818 | 12:112,441,632 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.