THNSL1
threonine synthase like 1
Summary
Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs274312 | 10:25,244,392 | C/T | upstream gene variant | — |
| rs187903288 | 10:25,260,891 | G/A | intergenic variant | — |
| rs770319378 | 10:25,312,226 | C/T | — | uncertain significance |
| rs1008307577 | 10:25,312,259 | C/T | — | uncertain significance |
| rs2491385666 | 10:25,312,297 | A/G | — | uncertain significance |
| rs1850765359 | 10:25,312,353 | G/A | — | likely benign |
| rs35746529 | 10:25,312,537 | A/C | — | uncertain significance |
| rs770856253 | 10:25,312,586 | T/C | — | uncertain significance |
| rs750985721 | 10:25,312,643 | G/A | — | uncertain significance |
| rs1482210012 | 10:25,312,679 | A/G | — | uncertain significance |
| rs1415118230 | 10:25,312,696 | A/G | — | uncertain significance |
| rs906064219 | 10:25,312,708 | C/A | — | uncertain significance |
| rs2491387638 | 10:25,312,786 | G/A | — | uncertain significance |
| rs770192962 | 10:25,312,835 | C/T | — | uncertain significance |
| rs2491388301 | 10:25,312,918 | A/G | — | uncertain significance |
| rs2491388474 | 10:25,312,962 | G/C | — | uncertain significance |
| rs549657853 | 10:25,312,984 | G/A | — | uncertain significance |
| rs772572245 | 10:25,313,023 | A/G | — | uncertain significance |
| rs770714996 | 10:25,313,164 | T/C | — | uncertain significance |
| rs2491389723 | 10:25,313,204 | A/C | — | uncertain significance |
| rs750181991 | 10:25,313,287 | T/G | — | uncertain significance |
| rs140014237 | 10:25,313,309 | T/C | — | uncertain significance |
| rs201692683 | 10:25,313,326 | C/T | — | uncertain significance |
| rs937412462 | 10:25,313,340 | T/A | — | uncertain significance |
| rs780227831 | 10:25,313,342 | A/G | — | uncertain significance |
| rs370053457 | 10:25,313,357 | C/T | — | uncertain significance |
| rs774623515 | 10:25,313,552 | C/T | — | uncertain significance |
| rs771043199 | 10:25,313,600 | A/G | — | uncertain significance |
| rs1289647382 | 10:25,313,608 | G/A | — | uncertain significance |
| rs150828849 | 10:25,313,617 | G/C | — | uncertain significance |
| rs752329040 | 10:25,313,745 | C/G | — | uncertain significance |
| rs1850812790 | 10:25,313,773 | A/T | — | uncertain significance |
| rs769011857 | 10:25,313,804 | T/C | — | uncertain significance |
| rs774998745 | 10:25,313,837 | C/T | — | uncertain significance |
| rs565199033 | 10:25,313,876 | A/G | — | uncertain significance |
| rs543682774 | 10:25,313,883 | C/A | — | uncertain significance |
| rs1399303142 | 10:25,313,890 | G/A | — | uncertain significance |
| rs1850818527 | 10:25,313,926 | A/G | — | uncertain significance |
| rs2491393225 | 10:25,313,966 | C/G | — | uncertain significance |
| rs1446736047 | 10:25,314,034 | A/G | — | uncertain significance |
| rs772276011 | 10:25,314,043 | A/G | — | uncertain significance |
| rs145306797 | 10:25,314,047 | A/G | — | uncertain significance |
| rs774289015 | 10:25,314,206 | A/G | — | uncertain significance |
| rs773981018 | 10:25,314,294 | G/T | — | uncertain significance |
| rs2491395043 | 10:25,314,337 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.