SLC22A7
solute carrier family 22 member 7
Summary
The protein encoded by this gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and appears to be localized to the basolateral membrane of the kidney. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs62415384 | 6:43,261,767 | G/T | — | — |
| rs62646255 | 6:43,262,303 | T/C | — | — |
| rs1196182957 | 6:43,266,112 | C/G | — | uncertain significance |
| rs770878980 | 6:43,266,121 | C/G | — | uncertain significance |
| rs764779971 | 6:43,266,130 | G/A | — | uncertain significance |
| rs368292121 | 6:43,266,140 | C/T | — | uncertain significance |
| rs766980028 | 6:43,266,251 | C/T | — | uncertain significance |
| rs35263175 | 6:43,266,318 | T/C | — | benign |
| rs371307824 | 6:43,266,341 | G/A | — | likely benign |
| rs146886850 | 6:43,266,831 | C/T | — | uncertain significance |
| rs1356408442 | 6:43,267,150 | A/G | — | uncertain significance |
| rs980845835 | 6:43,267,372 | C/T | — | uncertain significance |
| rs746272395 | 6:43,267,373 | G/A | — | uncertain significance |
| rs777787044 | 6:43,267,666 | C/T | — | uncertain significance |
| rs2534190457 | 6:43,267,684 | G/A | — | uncertain significance |
| rs1356990265 | 6:43,267,708 | T/G | — | uncertain significance |
| rs771464205 | 6:43,267,726 | T/C | — | uncertain significance |
| rs199806887 | 6:43,267,740 | C/T | — | uncertain significance |
| rs987817498 | 6:43,267,789 | G/A | — | uncertain significance |
| rs143456756 | 6:43,268,950 | C/T | — | uncertain significance |
| rs2841648 | 6:43,269,179 | C/A | downstream gene variant | — |
| rs56401710 | 6:43,269,180 | C/A | downstream gene variant | — |
| rs755426914 | 6:43,269,334 | T/C | — | uncertain significance |
| rs202177785 | 6:43,269,339 | G/A | — | uncertain significance |
| rs371403676 | 6:43,269,393 | C/T | — | uncertain significance |
| rs150649827 | 6:43,269,420 | G/A | — | likely benign |
| rs757872915 | 6:43,270,023 | G/A | — | uncertain significance |
| rs371184200 | 6:43,270,128 | G/A | — | uncertain significance |
| rs144507531 | 6:43,270,427 | G/A | — | uncertain significance |
| rs754571458 | 6:43,271,838 | C/A | — | uncertain significance |
| rs774908941 | 6:43,271,853 | G/A | — | uncertain significance |
| rs770337250 | 6:43,271,865 | C/T | — | uncertain significance |
| rs751130220 | 6:43,271,925 | T/G | — | uncertain significance |
| rs4149178 | 6:43,272,188 | A/G | downstream gene variant | — |
| rs369685026 | 6:43,272,441 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.