SLC35G1
solute carrier family 35 member G1
Summary
This gene encodes a transmembrane protein which is a member of the drug/metabolite transporter protein superfamily. The encoded protein may play a role in the regulation of calcium levels inside the cell. [provided by RefSeq, Sep 2016]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11187722 | 10:95,653,192 | C/A | upstream gene variant | — |
| rs2060303555 | 10:95,653,834 | C/T | — | uncertain significance |
| rs1415834671 | 10:95,653,845 | C/A | — | uncertain significance |
| rs527642937 | 10:95,653,867 | G/T | — | uncertain significance |
| rs764026321 | 10:95,653,875 | G/A | — | uncertain significance |
| rs1424089191 | 10:95,653,899 | G/C | — | uncertain significance |
| rs199500711 | 10:95,653,922 | G/T | — | uncertain significance |
| rs771072178 | 10:95,653,942 | C/T | — | uncertain significance |
| rs976091120 | 10:95,658,337 | A/G | — | uncertain significance |
| rs2493015062 | 10:95,658,358 | T/C | — | uncertain significance |
| rs1388383101 | 10:95,658,414 | G/C | — | uncertain significance |
| rs754389880 | 10:95,658,500 | A/G | — | uncertain significance |
| rs146091982 | 10:95,659,958 | A/G | intron variant | — |
| rs1267307676 | 10:95,660,522 | G/A | — | uncertain significance |
| rs779017955 | 10:95,660,559 | G/A | — | uncertain significance |
| rs144043787 | 10:95,660,576 | G/A | — | uncertain significance |
| rs201479419 | 10:95,660,592 | A/G | — | uncertain significance |
| rs2493020178 | 10:95,660,598 | C/T | — | uncertain significance |
| rs2493020600 | 10:95,660,690 | A/G | — | uncertain significance |
| rs144622838 | 10:95,660,754 | G/C | — | uncertain significance |
| rs145449600 | 10:95,660,774 | T/C | — | uncertain significance |
| rs144586382 | 10:95,660,784 | C/T | — | likely benign |
| rs199545587 | 10:95,660,939 | G/T | — | likely benign |
| rs201136283 | 10:95,661,013 | C/G | — | likely benign |
| rs760208308 | 10:95,661,021 | T/C | — | uncertain significance |
| rs749808552 | 10:95,661,024 | G/T | — | uncertain significance |
| rs2493022472 | 10:95,661,122 | G/C | — | uncertain significance |
| rs771902633 | 10:95,661,221 | C/A | — | uncertain significance |
| rs568345324 | 10:95,661,227 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.