SLC1A7
solute carrier family 1 member 7
Summary
Enables glutamate:sodium symporter activity. Involved in neurotransmitter uptake. Predicted to be located in photoreceptor cell terminal bouton. Predicted to be active in glutamatergic synapse; postsynaptic membrane; and presynaptic membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs140010762 | 1:53,553,714 | G/A | — | likely benign |
| rs2525244953 | 1:53,553,722 | G/A | — | uncertain significance |
| rs748161006 | 1:53,553,724 | T/G | — | uncertain significance |
| rs766880610 | 1:53,553,859 | T/G | — | uncertain significance |
| rs754734228 | 1:53,553,876 | C/G | — | uncertain significance |
| rs781446041 | 1:53,554,566 | G/A | — | uncertain significance |
| rs769301056 | 1:53,555,487 | G/T | — | uncertain significance |
| rs145443647 | 1:53,555,524 | C/T | — | uncertain significance |
| rs200606407 | 1:53,555,536 | C/T | — | uncertain significance |
| rs141869947 | 1:53,556,315 | C/T | — | uncertain significance |
| rs2525257957 | 1:53,556,381 | T/G | — | uncertain significance |
| rs374730599 | 1:53,556,410 | C/T | — | uncertain significance |
| rs1644412301 | 1:53,556,434 | T/C | — | uncertain significance |
| rs767569024 | 1:53,558,269 | C/G | — | uncertain significance |
| rs1288406 | 1:53,558,270 | A/G | — | benign |
| rs766773537 | 1:53,558,271 | C/T | — | uncertain significance |
| rs749261435 | 1:53,558,307 | A/C | — | uncertain significance |
| rs376317359 | 1:53,558,314 | G/A | — | uncertain significance |
| rs147574179 | 1:53,558,335 | C/T | — | uncertain significance |
| rs2525266954 | 1:53,558,381 | C/A | — | uncertain significance |
| rs199791615 | 1:53,558,391 | A/G | — | uncertain significance |
| rs139648137 | 1:53,558,404 | C/T | — | uncertain significance |
| rs370082225 | 1:53,558,459 | C/G | — | uncertain significance |
| rs759274735 | 1:53,559,158 | T/A | — | uncertain significance |
| rs775058993 | 1:53,559,163 | G/A | — | uncertain significance |
| rs763535754 | 1:53,559,226 | A/G | — | uncertain significance |
| rs58924052 | 1:53,565,054 | T/C | intron variant | — |
| rs2525335388 | 1:53,569,156 | C/T | — | uncertain significance |
| rs756513740 | 1:53,569,173 | C/T | — | uncertain significance |
| rs745618377 | 1:53,569,189 | C/T | — | uncertain significance |
| rs371840729 | 1:53,569,219 | C/T | — | uncertain significance |
| rs1312999214 | 1:53,569,224 | G/A | — | uncertain significance |
| rs527517279 | 1:53,569,236 | C/T | — | uncertain significance |
| rs369559497 | 1:53,571,432 | G/T | — | uncertain significance |
| rs2525379995 | 1:53,580,470 | G/C | — | uncertain significance |
| rs141274422 | 1:53,580,505 | G/A | — | uncertain significance |
| rs776189525 | 1:53,580,506 | C/T | — | uncertain significance |
| rs117636602 | 1:53,580,584 | C/T | — | uncertain significance |
| rs3820201 | 1:53,581,670 | A/T | coding sequence variant | — |
| rs3766800 | 1:53,593,913 | A/G | intron variant | — |
| rs780863782 | 1:53,608,000 | C/T | — | likely benign |
| rs775697947 | 1:53,608,004 | G/A | — | uncertain significance |
| rs1297803287 | 1:53,608,006 | G/A | — | uncertain significance |
| rs201010691 | 1:53,608,037 | C/T | — | uncertain significance |
| rs757953562 | 1:53,608,085 | C/T | — | uncertain significance |
| rs770118008 | 1:53,608,096 | C/G | — | uncertain significance |
| rs762380862 | 1:53,608,114 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.