SLC45A4
solute carrier family 45 member 4
Summary
Predicted to enable sucrose:proton symporter activity. Predicted to be involved in sucrose transport. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants111 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3739241 | 8:142,221,361 | C/G | 3 prime UTR variant | — |
| rs144361805 | 8:142,221,594 | C/T | — | likely benign |
| rs2552154723 | 8:142,221,628 | C/A | — | uncertain significance |
| rs1392907298 | 8:142,221,681 | C/A | — | uncertain significance |
| rs779358878 | 8:142,221,684 | A/G | — | likely benign |
| rs200439120 | 8:142,221,746 | C/T | — | uncertain significance |
| rs373975040 | 8:142,221,764 | C/T | — | uncertain significance |
| rs112375963 | 8:142,221,799 | A/G | — | benign |
| rs3824235 | 8:142,222,261 | A/G | intron variant | — |
| rs368838052 | 8:142,222,304 | C/G | — | uncertain significance |
| rs1436701613 | 8:142,222,306 | G/C | — | uncertain significance |
| rs147581518 | 8:142,222,315 | G/A | — | likely benign |
| rs150117417 | 8:142,222,329 | C/G | — | benign |
| rs145913953 | 8:142,222,331 | C/T | — | uncertain significance |
| rs114152576 | 8:142,222,338 | C/T | — | benign |
| rs374347167 | 8:142,222,442 | C/T | — | uncertain significance |
| rs770111752 | 8:142,222,508 | T/C | — | uncertain significance |
| rs375296684 | 8:142,222,520 | G/C | — | uncertain significance |
| rs753310131 | 8:142,222,523 | C/A | — | uncertain significance |
| rs754529727 | 8:142,222,532 | C/T | — | uncertain significance |
| rs947464317 | 8:142,222,613 | T/A | — | uncertain significance |
| rs2552155035 | 8:142,222,630 | G/C | — | uncertain significance |
| rs201350370 | 8:142,222,631 | A/C | — | uncertain significance |
| rs372268272 | 8:142,222,650 | G/C | — | uncertain significance |
| rs1825904461 | 8:142,222,654 | T/C | — | uncertain significance |
| rs2552155339 | 8:142,225,866 | T/C | — | uncertain significance |
| rs200395774 | 8:142,225,950 | C/T | — | uncertain significance |
| rs201000629 | 8:142,225,955 | T/C | — | uncertain significance |
| rs752835712 | 8:142,225,959 | C/T | — | uncertain significance |
| rs140681246 | 8:142,225,961 | C/T | — | benign |
| rs201465542 | 8:142,225,971 | T/C | — | uncertain significance |
| rs1464914963 | 8:142,226,049 | C/G | — | uncertain significance |
| rs542881539 | 8:142,227,270 | C/A | — | uncertain significance |
| rs61995889 | 8:142,227,271 | G/A | — | benign |
| rs10107024 | 8:142,227,592 | T/C | intron variant | — |
| rs9324542 | 8:142,227,854 | T/A | intron variant | — |
| rs774194996 | 8:142,228,130 | T/C | — | uncertain significance |
| rs2552156080 | 8:142,228,148 | C/T | — | uncertain significance |
| rs61995882 | 8:142,228,161 | G/T | — | benign |
| rs151178091 | 8:142,228,271 | C/T | — | uncertain significance |
| rs140273884 | 8:142,228,275 | C/T | — | likely benign |
| rs2552156155 | 8:142,228,276 | C/T | — | uncertain significance |
| rs1182411183 | 8:142,228,333 | C/T | — | uncertain significance |
| rs762686238 | 8:142,228,348 | C/T | — | uncertain significance |
| rs748393317 | 8:142,228,381 | C/T | — | uncertain significance |
| rs61995881 | 8:142,228,386 | C/T | — | benign |
| rs765333978 | 8:142,228,424 | G/A | — | uncertain significance |
| rs752852131 | 8:142,228,429 | C/T | — | uncertain significance |
| rs141507926 | 8:142,228,465 | C/T | — | uncertain significance |
| rs766781426 | 8:142,228,480 | C/T | — | uncertain significance |
| rs766675251 | 8:142,228,487 | C/T | — | uncertain significance |
| rs752833773 | 8:142,228,499 | G/A | — | uncertain significance |
| rs61995888 | 8:142,228,513 | G/A | — | benign |
| rs147338719 | 8:142,228,516 | G/A | — | uncertain significance |
| rs777432113 | 8:142,228,517 | T/A | — | uncertain significance |
| rs764105621 | 8:142,228,540 | C/A | — | uncertain significance |
| rs144230271 | 8:142,228,545 | G/A | — | benign |
| rs375752623 | 8:142,228,550 | C/T | — | uncertain significance |
| rs569786400 | 8:142,228,631 | C/T | — | uncertain significance |
| rs142593631 | 8:142,228,635 | C/T | — | benign |
| rs141057293 | 8:142,228,658 | T/C | — | uncertain significance |
| rs374109656 | 8:142,228,666 | C/T | — | uncertain significance |
| rs2552156416 | 8:142,228,682 | T/G | — | uncertain significance |
| rs368211710 | 8:142,228,685 | C/G | — | uncertain significance |
| rs138770433 | 8:142,228,706 | G/A | — | uncertain significance |
| rs375980527 | 8:142,228,728 | G/C | — | uncertain significance |
| rs368300870 | 8:142,228,754 | C/T | — | uncertain significance |
| rs2552156477 | 8:142,228,769 | G/T | — | uncertain significance |
| rs761731003 | 8:142,228,796 | C/T | — | uncertain significance |
| rs564741519 | 8:142,228,810 | G/A | — | likely benign |
| rs559626893 | 8:142,228,841 | C/T | — | uncertain significance |
| rs751947546 | 8:142,228,873 | G/A | — | uncertain significance |
| rs750552377 | 8:142,228,881 | C/A | — | uncertain significance |
| rs749540390 | 8:142,228,888 | G/A | — | uncertain significance |
| rs777556052 | 8:142,228,901 | C/T | — | likely benign |
| rs144566162 | 8:142,228,923 | C/T | — | benign |
| rs756143827 | 8:142,228,928 | C/T | — | uncertain significance |
| rs755250211 | 8:142,228,930 | C/T | — | uncertain significance |
| rs139911158 | 8:142,228,943 | C/G | — | uncertain significance |
| rs369040693 | 8:142,228,948 | C/T | — | uncertain significance |
| rs763779178 | 8:142,229,056 | C/T | — | uncertain significance |
| rs750313707 | 8:142,229,071 | A/T | — | uncertain significance |
| rs1329860731 | 8:142,229,083 | G/A | — | uncertain significance |
| rs747821881 | 8:142,229,105 | C/T | — | uncertain significance |
| rs3739235 | 8:142,229,145 | A/G | intron variant | — |
| rs2304282 | 8:142,229,543 | A/C | — | — |
| rs115384487 | 8:142,229,786 | C/T | — | benign |
| rs2552157215 | 8:142,229,847 | C/T | — | uncertain significance |
| rs768644390 | 8:142,229,877 | G/A | — | uncertain significance |
| rs753261584 | 8:142,229,893 | T/C | — | uncertain significance |
| rs766115317 | 8:142,229,914 | C/T | — | uncertain significance |
| rs55714105 | 8:142,229,915 | G/T | — | benign |
| rs1268722671 | 8:142,229,916 | C/A | — | uncertain significance |
| rs10101692 | 8:142,230,823 | C/A | — | — |
| rs150530787 | 8:142,231,706 | C/T | — | uncertain significance |
| rs757182744 | 8:142,231,736 | G/A | — | uncertain significance |
| rs780845132 | 8:142,231,748 | G/C | — | uncertain significance |
| rs745427921 | 8:142,231,750 | C/T | — | uncertain significance |
| rs1267959102 | 8:142,231,761 | G/C | — | uncertain significance |
| rs139360300 | 8:142,231,766 | G/A | — | likely benign |
Showing 100 of 111 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.