RPS6KA5
ribosomal protein S6 kinase A5
Summary
Enables ATP binding activity and protein kinase activity. Involved in several processes, including interleukin-1-mediated signaling pathway; protein modification process; and regulation of DNA-templated transcription. Located in cytoplasm and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs75055810 | 14:91,329,386 | T/A | — | — |
| rs756443629 | 14:91,338,455 | G/A | — | uncertain significance |
| rs543409817 | 14:91,338,465 | T/C | — | likely benign |
| rs200886537 | 14:91,338,467 | T/A | — | uncertain significance |
| rs149441965 | 14:91,338,561 | G/A | — | uncertain significance |
| rs767977575 | 14:91,340,047 | G/C | — | uncertain significance |
| rs2503516368 | 14:91,340,134 | G/T | — | uncertain significance |
| rs759640790 | 14:91,341,602 | A/T | — | uncertain significance |
| rs139155141 | 14:91,341,606 | A/C | — | uncertain significance |
| rs376770842 | 14:91,341,646 | G/C | — | uncertain significance |
| rs1362709766 | 14:91,341,650 | A/G | — | uncertain significance |
| rs182308463 | 14:91,341,703 | T/C | — | uncertain significance |
| rs76750653 | 14:91,344,156 | A/C | intron variant | — |
| rs2503621713 | 14:91,356,914 | T/G | — | uncertain significance |
| rs2503649468 | 14:91,360,861 | T/G | — | uncertain significance |
| rs537754207 | 14:91,360,875 | C/T | — | uncertain significance |
| rs184182212 | 14:91,365,831 | C/T | intron variant | — |
| rs369503281 | 14:91,366,509 | C/T | — | uncertain significance |
| rs745922176 | 14:91,366,996 | G/A | — | uncertain significance |
| rs2503708805 | 14:91,369,183 | G/A | — | uncertain significance |
| rs200895075 | 14:91,369,203 | A/T | — | uncertain significance |
| rs376247617 | 14:91,369,289 | C/T | — | uncertain significance |
| rs754944278 | 14:91,369,313 | T/C | — | uncertain significance |
| rs371531566 | 14:91,372,611 | T/C | — | uncertain significance |
| rs746195386 | 14:91,386,584 | C/G | — | uncertain significance |
| rs1455680711 | 14:91,386,619 | T/C | — | uncertain significance |
| rs12896373 | 14:91,398,735 | C/G | — | — |
| rs200296811 | 14:91,413,787 | G/C | — | uncertain significance |
| rs781411551 | 14:91,413,831 | T/G | — | uncertain significance |
| rs778788639 | 14:91,413,846 | C/T | — | uncertain significance |
| rs1286083 | 14:91,442,779 | T/C | intron variant | — |
| rs756086272 | 14:91,444,844 | C/T | — | uncertain significance |
| rs151225102 | 14:91,444,845 | G/A | — | uncertain significance |
| rs1286079 | 14:91,445,162 | C/T | intron variant | — |
| rs1286075 | 14:91,446,796 | C/T | intron variant | — |
| rs1286065 | 14:91,451,783 | C/T | intron variant | — |
| rs8005489 | 14:91,473,271 | G/A | intron variant | — |
| rs1951456 | 14:91,512,340 | T/C | intron variant | — |
| rs1285997 | 14:91,513,029 | C/G | intron variant | — |
| rs1285990 | 14:91,522,114 | C/G | — | — |
| rs1285988 | 14:91,523,390 | A/C | — | — |
| rs1018548 | 14:91,524,303 | G/T | — | — |
| rs1399772704 | 14:91,526,687 | T/A | — | uncertain significance |
| rs749352681 | 14:91,526,717 | C/A | — | uncertain significance |
| rs776541777 | 14:91,526,723 | C/A | — | uncertain significance |
| rs765224867 | 14:91,526,727 | C/G | — | uncertain significance |
| rs2542908171 | 14:91,526,729 | T/C | — | uncertain significance |
| rs372919173 | 14:91,526,757 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.