SLC22A31
solute carrier family 22 member 31
Summary
Predicted to enable transmembrane transporter activity. Predicted to be involved in monoatomic ion transport and transmembrane transport. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs35146933 | 16:89,262,419 | G/A | synonymous variant | — |
| rs1597316476 | 16:89,262,430 | C/T | — | uncertain significance |
| rs2287353 | 16:89,262,431 | A/G | — | benign |
| rs746123571 | 16:89,262,490 | G/A | — | uncertain significance |
| rs775748555 | 16:89,262,514 | G/A | — | uncertain significance |
| rs575619368 | 16:89,262,517 | C/T | — | uncertain significance |
| rs762545736 | 16:89,262,552 | C/T | — | uncertain significance |
| rs1160674190 | 16:89,262,559 | C/G | — | uncertain significance |
| rs756021552 | 16:89,262,594 | G/C | — | uncertain significance |
| rs559452735 | 16:89,262,636 | C/T | — | uncertain significance |
| rs117169628 | 16:89,262,657 | G/A | — | benign |
| rs190309297 | 16:89,263,715 | G/T | — | uncertain significance |
| rs757216093 | 16:89,263,728 | C/T | — | uncertain significance |
| rs750483546 | 16:89,263,733 | G/A | — | uncertain significance |
| rs763607214 | 16:89,264,575 | T/C | — | uncertain significance |
| rs575460192 | 16:89,264,619 | G/A | — | uncertain significance |
| rs1239914383 | 16:89,264,712 | C/T | — | uncertain significance |
| rs541130567 | 16:89,264,868 | A/G | — | uncertain significance |
| rs1313859758 | 16:89,264,907 | A/T | — | uncertain significance |
| rs1916200754 | 16:89,264,908 | G/T | — | uncertain significance |
| rs984116803 | 16:89,264,922 | C/T | — | likely benign |
| rs61732365 | 16:89,265,087 | G/A | — | benign |
| rs1916228802 | 16:89,265,088 | A/T | — | uncertain significance |
| rs534025935 | 16:89,265,089 | C/A | — | uncertain significance |
| rs74640353 | 16:89,265,101 | C/T | — | benign |
| rs758202617 | 16:89,265,125 | C/T | — | likely benign |
| rs1916239066 | 16:89,265,143 | G/C | — | uncertain significance |
| rs561469047 | 16:89,265,202 | G/T | — | uncertain significance |
| rs375247169 | 16:89,265,452 | C/A | — | uncertain significance |
| rs1318787376 | 16:89,265,470 | A/G | — | uncertain significance |
| rs554493532 | 16:89,265,503 | G/A | — | uncertain significance |
| rs1916295137 | 16:89,265,540 | A/G | — | uncertain significance |
| rs547557634 | 16:89,265,548 | C/G | — | uncertain significance |
| rs529150802 | 16:89,268,323 | G/C | — | — |
| rs559329225 | 16:89,269,154 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.