STK32A
serine/threonine kinase 32A
Summary
Predicted to enable protein serine/threonine kinase activity. Predicted to be involved in intracellular signal transduction. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs190535913 | 5:146,619,204 | G/A | — | uncertain significance |
| rs373265374 | 5:146,619,221 | A/T | — | uncertain significance |
| rs1301403467 | 5:146,619,235 | A/G | — | uncertain significance |
| rs570834819 | 5:146,636,820 | G/T | — | — |
| rs772852698 | 5:146,657,714 | G/A | — | uncertain significance |
| rs776005093 | 5:146,658,835 | C/T | — | uncertain significance |
| rs2480437646 | 5:146,658,883 | A/T | — | uncertain significance |
| rs374431900 | 5:146,658,914 | A/C | — | uncertain significance |
| rs1233966528 | 5:146,658,931 | G/T | — | uncertain significance |
| rs549432880 | 5:146,673,926 | G/A | — | — |
| rs10875622 | 5:146,693,062 | G/A | intron variant | — |
| rs200548298 | 5:146,703,526 | G/A | — | uncertain significance |
| rs2480585062 | 5:146,703,588 | C/A | — | uncertain significance |
| rs142623619 | 5:146,730,251 | A/C | intron variant | — |
| rs370511823 | 5:146,730,642 | A/G | — | uncertain significance |
| rs371782826 | 5:146,730,661 | C/T | — | uncertain significance |
| rs4705038 | 5:146,733,598 | C/A | intron variant | — |
| rs2480696508 | 5:146,741,087 | G/C | — | uncertain significance |
| rs1287398426 | 5:146,741,090 | G/A | — | uncertain significance |
| rs376225585 | 5:146,741,176 | G/A | — | uncertain significance |
| rs1338135539 | 5:146,750,245 | C/T | — | uncertain significance |
| rs199544939 | 5:146,750,259 | G/A | — | uncertain significance |
| rs1041836239 | 5:146,750,310 | G/A | — | uncertain significance |
| rs749535396 | 5:146,750,320 | C/T | — | uncertain significance |
| rs1369485464 | 5:146,750,325 | C/G | — | uncertain significance |
| rs926595749 | 5:146,750,326 | T/C | — | uncertain significance |
| rs199893483 | 5:146,752,757 | G/A | — | uncertain significance |
| rs1757079777 | 5:146,752,790 | C/T | — | uncertain significance |
| rs770604801 | 5:146,752,820 | T/A | — | uncertain significance |
| rs1757081934 | 5:146,752,829 | A/G | — | uncertain significance |
| rs368176756 | 5:146,754,734 | C/A | — | uncertain significance |
| rs753585311 | 5:146,754,735 | G/A | — | uncertain significance |
| rs779824878 | 5:146,754,759 | T/A | — | uncertain significance |
| rs1187465155 | 5:146,763,485 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.