SLC28A1
solute carrier family 28 member 1
Summary
Enables azole transmembrane transporter activity; pyrimidine- and adenosine-specific:sodium symporter activity; and uridine transmembrane transporter activity. Involved in azole transmembrane transport and nucleoside transport. Located in apical plasma membrane; cytosol; and nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants71 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs114615130 | 15:85,430,019 | G/A | splice region variant | — |
| rs3743162 | 15:85,430,969 | C/G | — | — |
| rs8187737 | 15:85,431,000 | C/T | — | benign |
| rs772174865 | 15:85,431,061 | A/C | — | uncertain significance |
| rs1427920379 | 15:85,431,062 | T/A | — | uncertain significance |
| rs8187742 | 15:85,431,993 | C/T | — | likely benign |
| rs17222302 | 15:85,432,030 | C/T | — | benign |
| rs17222295 | 15:85,432,034 | G/A | — | benign |
| rs1196209657 | 15:85,432,073 | C/G | — | uncertain significance |
| rs1030637478 | 15:85,438,195 | C/T | — | uncertain significance |
| rs2505869678 | 15:85,438,224 | G/A | — | uncertain significance |
| rs759745634 | 15:85,438,269 | C/T | — | uncertain significance |
| rs2505870759 | 15:85,438,279 | A/C | — | uncertain significance |
| rs116707209 | 15:85,438,333 | G/A | — | likely benign |
| rs760090743 | 15:85,438,341 | C/A | — | uncertain significance |
| rs769108342 | 15:85,438,651 | C/G | — | likely benign |
| rs748632234 | 15:85,447,330 | G/T | — | uncertain significance |
| rs772788617 | 15:85,447,378 | A/G | — | uncertain significance |
| rs2290272 | 15:85,447,431 | G/A | missense variant | benign |
| rs45523532 | 15:85,447,434 | T/G | — | benign |
| rs780352916 | 15:85,447,458 | C/T | — | uncertain significance |
| rs777812483 | 15:85,447,467 | G/A | — | uncertain significance |
| rs781041305 | 15:85,448,778 | G/C | — | uncertain significance |
| rs8187755 | 15:85,448,796 | A/T | — | benign |
| rs781164267 | 15:85,448,852 | T/C | — | uncertain significance |
| rs8187758 | 15:85,448,875 | C/A | — | benign |
| rs765445721 | 15:85,448,881 | C/T | — | uncertain significance |
| rs893460533 | 15:85,451,985 | G/A | — | uncertain significance |
| rs762965574 | 15:85,451,989 | T/C | — | uncertain significance |
| rs145516173 | 15:85,461,750 | G/A | — | benign |
| rs17215975 | 15:85,461,794 | G/A | — | likely benign |
| rs756412017 | 15:85,464,262 | G/A | — | uncertain significance |
| rs3825875 | 15:85,467,207 | C/T | — | benign |
| rs139484056 | 15:85,467,271 | T/C | — | uncertain significance |
| rs3803390 | 15:85,467,275 | C/T | — | benign |
| rs1341701454 | 15:85,467,297 | G/A | — | uncertain significance |
| rs760798468 | 15:85,467,322 | G/A | — | uncertain significance |
| rs994238470 | 15:85,467,334 | C/G | — | uncertain significance |
| rs116191689 | 15:85,468,278 | C/T | regulatory region variant | — |
| rs17222379 | 15:85,476,390 | G/A | — | likely benign |
| rs2305367 | 15:85,476,441 | G/A | — | benign |
| rs748592691 | 15:85,476,452 | C/T | — | uncertain significance |
| rs370097368 | 15:85,476,500 | C/G | — | uncertain significance |
| rs781741336 | 15:85,478,306 | G/A | — | uncertain significance |
| rs746351142 | 15:85,478,311 | G/C | — | uncertain significance |
| rs141441409 | 15:85,478,343 | C/T | — | uncertain significance |
| rs754985427 | 15:85,478,408 | C/G | — | uncertain significance |
| rs2242048 | 15:85,478,410 | A/G | synonymous variant | benign |
| rs1465637315 | 15:85,478,557 | C/G | — | uncertain significance |
| rs8187779 | 15:85,478,573 | C/A | — | benign |
| rs1035660741 | 15:85,478,657 | G/A | — | uncertain significance |
| rs2242047 | 15:85,478,696 | C/T | missense variant | benign |
| rs757554044 | 15:85,478,700 | G/A | — | uncertain significance |
| rs2242046 | 15:85,478,729 | G/A | missense variant | benign |
| rs45584739 | 15:85,486,730 | T/C | missense variant | benign |
| rs149246522 | 15:85,487,815 | G/A | — | affects |
| rs748010707 | 15:85,487,884 | C/G | — | uncertain significance |
| rs762518942 | 15:85,487,992 | C/T | — | uncertain significance |
| rs970673161 | 15:85,488,005 | G/A | — | uncertain significance |
| rs756560653 | 15:85,488,019 | G/C | — | uncertain significance |
| rs17222414 | 15:85,488,348 | C/G | — | benign |
| rs115647635 | 15:85,488,399 | C/T | — | uncertain significance |
| rs72547520 | 15:85,488,439 | A/G | — | benign |
| rs201090642 | 15:85,499,703 | T/C | — | — |
| rs72754973 | 15:85,501,006 | T/G | intron variant | — |
| rs72754976 | 15:85,503,279 | A/G | intron variant | — |
| rs111460093 | 15:85,504,753 | G/C | — | benign |
| rs112431612 | 15:85,504,762 | A/T | — | benign |
| rs112595560 | 15:85,505,400 | A/G | intron variant | — |
| rs113752636 | 15:85,509,596 | C/G | intron variant | — |
| rs147728564 | 15:85,518,763 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.