STK17A
serine/threonine kinase 17a
Summary
This gene is a member of the DAP kinase-related apoptosis-inducing protein kinase family and encodes an autophosphorylated nuclear protein with a protein kinase domain. The protein has apoptosis-inducing activity. [provided by RefSeq, Jul 2008]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs904358428 | 7:43,622,870 | G/T | — | uncertain significance |
| rs768808965 | 7:43,622,955 | A/G | — | uncertain significance |
| rs1028481524 | 7:43,622,979 | T/C | — | uncertain significance |
| rs760666031 | 7:43,623,030 | C/T | — | uncertain significance |
| rs2241738 | 7:43,623,123 | C/G | regulatory region variant | — |
| rs771565115 | 7:43,635,598 | G/A | — | uncertain significance |
| rs902934302 | 7:43,635,657 | A/G | — | uncertain significance |
| rs10232580 | 7:43,637,228 | T/C | intron variant | — |
| rs77026432 | 7:43,647,938 | G/A | — | likely benign |
| rs771807800 | 7:43,647,942 | G/C | — | uncertain significance |
| rs1344351458 | 7:43,647,944 | T/C | — | uncertain significance |
| rs746632915 | 7:43,647,955 | G/A | — | uncertain significance |
| rs770356144 | 7:43,647,973 | C/G | — | uncertain significance |
| rs776064671 | 7:43,647,974 | G/A | — | likely benign |
| rs7805969 | 7:43,651,047 | A/G | intron variant | — |
| rs34064273 | 7:43,654,932 | G/A | intron variant | — |
| rs139022225 | 7:43,659,242 | A/T | — | uncertain significance |
| rs566758223 | 7:43,659,244 | A/C | — | uncertain significance |
| rs2230753 | 7:43,663,184 | T/C | — | benign |
| rs144785063 | 7:43,663,216 | T/C | — | uncertain significance |
| rs2538456860 | 7:43,663,328 | A/G | — | uncertain significance |
| rs559296227 | 7:43,663,364 | A/G | — | uncertain significance |
| rs753382535 | 7:43,663,365 | T/A | — | uncertain significance |
| rs1339648808 | 7:43,663,381 | T/C | — | uncertain significance |
| rs976300914 | 7:43,664,151 | C/T | — | uncertain significance |
| rs749011542 | 7:43,664,332 | G/C | — | uncertain significance |
| rs963663218 | 7:43,664,398 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.