STKLD1
serine/threonine kinase like domain containing 1
Summary
Predicted to enable protein serine/threonine kinase activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs587658612 | 9:136,243,379 | C/T | — | uncertain significance |
| rs374824261 | 9:136,243,406 | C/T | — | uncertain significance |
| rs782806956 | 9:136,243,414 | C/T | — | uncertain significance |
| rs587734057 | 9:136,243,428 | C/A | — | uncertain significance |
| rs146900935 | 9:136,245,917 | A/G | — | likely benign |
| rs782398798 | 9:136,249,664 | G/A | — | uncertain significance |
| rs41316980 | 9:136,249,856 | G/A | intron variant | — |
| rs782779585 | 9:136,250,175 | G/A | — | — |
| rs369047700 | 9:136,251,427 | C/G | — | uncertain significance |
| rs1838248585 | 9:136,251,455 | T/C | — | uncertain significance |
| rs188110518 | 9:136,252,318 | G/A | regulatory region variant | — |
| rs1838291925 | 9:136,253,320 | C/G | — | uncertain significance |
| rs782040685 | 9:136,253,326 | C/G | — | uncertain significance |
| rs782312478 | 9:136,255,350 | A/T | — | uncertain significance |
| rs36048509 | 9:136,255,850 | G/C | intron variant | — |
| rs782698733 | 9:136,256,497 | C/A | — | uncertain significance |
| rs2490872488 | 9:136,256,534 | T/A | — | uncertain significance |
| rs2490872605 | 9:136,256,563 | G/A | — | uncertain significance |
| rs587672490 | 9:136,256,564 | C/T | — | uncertain significance |
| rs28394600 | 9:136,259,340 | C/G | intron variant | — |
| rs200576190 | 9:136,259,419 | C/T | — | likely benign |
| rs782160965 | 9:136,259,438 | A/T | — | uncertain significance |
| rs749647813 | 9:136,260,748 | C/T | — | uncertain significance |
| rs2490889661 | 9:136,260,793 | A/G | — | uncertain significance |
| rs782647523 | 9:136,260,818 | C/T | — | uncertain significance |
| rs782717621 | 9:136,262,308 | C/G | — | uncertain significance |
| rs2490895285 | 9:136,263,102 | T/G | — | uncertain significance |
| rs368025940 | 9:136,263,104 | A/G | — | uncertain significance |
| rs781883892 | 9:136,263,105 | T/A | — | uncertain significance |
| rs2490905771 | 9:136,266,936 | T/C | — | uncertain significance |
| rs782508745 | 9:136,266,957 | A/G | — | uncertain significance |
| rs150111949 | 9:136,266,962 | C/A | — | likely benign |
| rs2490906071 | 9:136,266,996 | C/T | — | likely benign |
| rs144696692 | 9:136,268,037 | A/G | — | uncertain significance |
| rs200211240 | 9:136,268,060 | C/A | — | uncertain significance |
| rs782532262 | 9:136,268,115 | G/A | — | uncertain significance |
| rs1554778127 | 9:136,268,848 | T/C | — | uncertain significance |
| rs147923253 | 9:136,268,860 | C/T | — | uncertain significance |
| rs376801977 | 9:136,268,893 | C/G | — | uncertain significance |
| rs369512252 | 9:136,268,896 | C/T | — | uncertain significance |
| rs782275526 | 9:136,268,925 | G/A | — | uncertain significance |
| rs782358062 | 9:136,268,944 | C/A | — | uncertain significance |
| rs201085864 | 9:136,269,142 | C/T | — | uncertain significance |
| rs186469807 | 9:136,269,429 | G/C | regulatory region variant | — |
| rs1554778380 | 9:136,269,926 | C/A | — | likely benign |
| rs781928239 | 9:136,269,970 | T/C | — | uncertain significance |
| rs2490917144 | 9:136,270,002 | C/G | — | uncertain significance |
| rs374471690 | 9:136,270,020 | G/A | — | uncertain significance |
| rs1321765288 | 9:136,270,027 | T/G | — | uncertain significance |
| rs41302673 | 9:136,270,538 | G/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.