SLC6A16
solute carrier family 6 member 16
Summary
SLC6A16 shows structural characteristics of an Na(+)- and Cl(-)-dependent neurotransmitter transporter, including 12 transmembrane (TM) domains, intracellular N and C termini, and large extracellular loops containing multiple N-glycosylation sites.[supplied by OMIM, Mar 2008]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs753409719 | 19:49,793,500 | C/T | — | likely benign |
| rs758392741 | 19:49,793,514 | C/T | — | likely benign |
| rs369578264 | 19:49,793,518 | C/G | — | uncertain significance |
| rs374643137 | 19:49,793,529 | A/G | — | uncertain significance |
| rs377694900 | 19:49,793,547 | G/A | — | uncertain significance |
| rs761892206 | 19:49,793,595 | G/T | — | uncertain significance |
| rs368464579 | 19:49,793,633 | C/T | — | uncertain significance |
| rs201025364 | 19:49,796,576 | A/G | — | uncertain significance |
| rs1970129481 | 19:49,797,146 | C/A | — | uncertain significance |
| rs2514325188 | 19:49,797,152 | A/G | — | uncertain significance |
| rs1268789887 | 19:49,797,234 | A/G | — | uncertain significance |
| rs2514326823 | 19:49,797,276 | C/T | — | uncertain significance |
| rs138253216 | 19:49,797,664 | C/T | missense variant | — |
| rs111914101 | 19:49,797,665 | G/A | — | uncertain significance |
| rs1970145937 | 19:49,797,712 | T/C | — | uncertain significance |
| rs1452248110 | 19:49,797,713 | T/C | — | uncertain significance |
| rs199810151 | 19:49,797,769 | A/G | — | uncertain significance |
| rs544732904 | 19:49,812,271 | A/G | — | uncertain significance |
| rs369751841 | 19:49,812,293 | C/T | — | likely benign |
| rs143434861 | 19:49,812,355 | A/G | — | uncertain significance |
| rs751710599 | 19:49,812,370 | G/A | — | uncertain significance |
| rs551058122 | 19:49,812,590 | T/C | — | uncertain significance |
| rs367909942 | 19:49,812,930 | T/C | — | uncertain significance |
| rs372514145 | 19:49,812,932 | G/C | — | uncertain significance |
| rs374177563 | 19:49,812,936 | A/T | — | uncertain significance |
| rs1251657530 | 19:49,812,972 | G/A | — | uncertain significance |
| rs1397993520 | 19:49,813,046 | G/C | — | uncertain significance |
| rs2514405406 | 19:49,813,052 | T/C | — | likely benign |
| rs979946445 | 19:49,813,063 | T/C | — | likely benign |
| rs200575419 | 19:49,813,395 | T/C | — | uncertain significance |
| rs769299339 | 19:49,813,669 | T/C | — | uncertain significance |
| rs2514412360 | 19:49,813,674 | C/T | — | uncertain significance |
| rs370627761 | 19:49,813,681 | G/A | — | uncertain significance |
| rs2514412995 | 19:49,813,723 | C/T | — | likely benign |
| rs189659673 | 19:49,813,759 | C/T | — | uncertain significance |
| rs2514416681 | 19:49,814,231 | C/A | — | uncertain significance |
| rs1970509401 | 19:49,814,285 | G/C | — | uncertain significance |
| rs201814152 | 19:49,814,294 | G/A | — | uncertain significance |
| rs373862770 | 19:49,814,298 | G/A | — | uncertain significance |
| rs201259913 | 19:49,814,326 | C/G | — | uncertain significance |
| rs201901598 | 19:49,814,539 | A/C | — | uncertain significance |
| rs2514419440 | 19:49,814,544 | C/A | — | uncertain significance |
| rs756089172 | 19:49,814,591 | G/A | — | uncertain significance |
| rs529063015 | 19:49,819,422 | T/A | — | — |
| rs138685407 | 19:49,831,161 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.