SLC26A9
solute carrier family 26 member 9
Summary
This gene is one member of a family of sulfate/anion transporter genes. Family members are well conserved in their genomic (number and size of exons) and protein (aa length among species) structures yet have markedly different tissue expression patterns. The product of this gene is a highly selective chloride ion channel regulated by WNK kinases. Alternative splicing results in multiple transcript variants encoding differing isoforms.[provided by RefSeq, Dec 2008]
Known Variants65 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs147477683 | 1:205,881,827 | C/T | downstream gene variant | — |
| rs9438438 | 1:205,884,062 | C/T | — | benign |
| rs748961360 | 1:205,884,103 | C/T | — | uncertain significance |
| rs1658522191 | 1:205,884,207 | G/A | — | uncertain significance |
| rs34309781 | 1:205,884,226 | C/T | — | likely benign |
| rs373591316 | 1:205,884,240 | C/T | — | uncertain significance |
| rs764909473 | 1:205,884,253 | G/A | — | uncertain significance |
| rs6669481 | 1:205,884,274 | T/C | — | benign |
| rs766846418 | 1:205,884,291 | C/T | — | uncertain significance |
| rs763900415 | 1:205,884,309 | T/C | — | uncertain significance |
| rs150227907 | 1:205,886,418 | A/G | — | uncertain significance |
| rs758627816 | 1:205,886,434 | G/A | — | uncertain significance |
| rs375480238 | 1:205,886,453 | G/A | — | likely benign |
| rs1445687345 | 1:205,886,454 | T/C | — | uncertain significance |
| rs16856462 | 1:205,887,981 | C/T | — | benign |
| rs1200348101 | 1:205,887,987 | G/T | — | uncertain significance |
| rs139528306 | 1:205,888,048 | C/T | — | uncertain significance |
| rs2526893322 | 1:205,888,071 | T/C | — | uncertain significance |
| rs199775815 | 1:205,889,310 | T/C | — | uncertain significance |
| rs16856470 | 1:205,889,329 | C/T | — | benign |
| rs2526898243 | 1:205,889,354 | C/G | — | uncertain significance |
| rs12759719 | 1:205,890,679 | T/C | — | benign |
| rs750399780 | 1:205,890,715 | C/T | — | uncertain significance |
| rs768396652 | 1:205,890,786 | T/C | — | uncertain significance |
| rs143272963 | 1:205,890,822 | C/T | — | uncertain significance |
| rs1658842373 | 1:205,890,864 | G/A | — | uncertain significance |
| rs34992672 | 1:205,890,885 | C/T | missense variant | — |
| rs2526910801 | 1:205,892,289 | T/C | — | uncertain significance |
| rs749520143 | 1:205,892,710 | C/T | — | uncertain significance |
| rs201456648 | 1:205,893,512 | A/G | — | uncertain significance |
| rs762496820 | 1:205,893,539 | C/G | — | uncertain significance |
| rs1259513095 | 1:205,893,559 | G/A | — | uncertain significance |
| rs1424801550 | 1:205,895,733 | A/G | — | uncertain significance |
| rs574530028 | 1:205,895,737 | C/T | — | uncertain significance |
| rs11240594 | 1:205,896,235 | G/A | intron variant | — |
| rs556910067 | 1:205,896,377 | T/G | — | uncertain significance |
| rs371663342 | 1:205,896,637 | C/T | — | uncertain significance |
| rs775998835 | 1:205,896,655 | T/C | — | uncertain significance |
| rs2526931910 | 1:205,896,679 | C/T | — | uncertain significance |
| rs143557818 | 1:205,897,044 | C/T | — | uncertain significance |
| rs1394910897 | 1:205,897,058 | T/C | — | uncertain significance |
| rs759057060 | 1:205,897,073 | C/T | — | uncertain significance |
| rs769381035 | 1:205,897,160 | G/A | — | likely benign |
| rs143942129 | 1:205,897,982 | A/G | — | uncertain significance |
| rs761061342 | 1:205,898,360 | C/T | — | uncertain significance |
| rs1344981323 | 1:205,898,402 | A/T | — | uncertain significance |
| rs371286295 | 1:205,898,421 | T/G | — | uncertain significance |
| rs771296518 | 1:205,898,451 | T/C | — | uncertain significance |
| rs143411715 | 1:205,898,454 | G/A | — | uncertain significance |
| rs141320922 | 1:205,898,466 | T/C | — | uncertain significance |
| rs139120548 | 1:205,898,470 | A/C | — | uncertain significance |
| rs538145477 | 1:205,899,025 | C/T | — | uncertain significance |
| rs1659237197 | 1:205,899,045 | T/A | — | uncertain significance |
| rs2526945483 | 1:205,899,066 | A/G | — | uncertain significance |
| rs780175202 | 1:205,899,106 | C/T | — | uncertain significance |
| rs773009094 | 1:205,899,123 | C/G | — | uncertain significance |
| rs146704092 | 1:205,901,026 | T/C | — | uncertain significance |
| rs141991495 | 1:205,901,152 | C/T | — | uncertain significance |
| rs775212275 | 1:205,902,093 | C/G | — | uncertain significance |
| rs1412352281 | 1:205,902,097 | C/T | — | uncertain significance |
| rs1349183780 | 1:205,902,100 | T/C | — | uncertain significance |
| rs1419975955 | 1:205,902,169 | G/A | — | uncertain significance |
| rs755293789 | 1:205,904,836 | C/A | — | uncertain significance |
| rs369903387 | 1:205,904,924 | C/T | — | uncertain significance |
| rs375875287 | 1:205,904,929 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.