TSNARE1
t-SNARE domain containing 1
Summary
Predicted to enable SNAP receptor activity and SNARE binding activity. Predicted to be involved in intracellular protein transport; vesicle docking; and vesicle fusion. Predicted to be located in membrane. Predicted to be part of SNARE complex. Predicted to be active in synaptic vesicle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11988455 | 8:143,310,853 | G/A | — | benign |
| rs139117582 | 8:143,310,927 | T/G | — | uncertain significance |
| rs4129585 | 8:143,312,933 | A/C | regulatory region variant | — |
| rs13262595 | 8:143,316,970 | A/C | — | — |
| rs75826611 | 8:143,323,591 | A/C | — | — |
| rs6985751 | 8:143,328,290 | A/C | — | — |
| rs548577819 | 8:143,333,095 | C/T | — | — |
| rs7012636 | 8:143,333,231 | A/T | — | — |
| rs67736411 | 8:143,336,546 | G/C | intron variant | — |
| rs898206027 | 8:143,356,173 | C/T | — | uncertain significance |
| rs762992416 | 8:143,356,174 | G/A | — | uncertain significance |
| rs755565732 | 8:143,356,203 | T/C | — | uncertain significance |
| rs141086701 | 8:143,361,458 | G/A | intron variant | — |
| rs13275517 | 8:143,364,521 | T/C | intron variant | — |
| rs1822338516 | 8:143,365,813 | C/T | — | uncertain significance |
| rs1563828092 | 8:143,365,817 | G/C | — | uncertain significance |
| rs537884081 | 8:143,365,838 | C/T | — | likely benign |
| rs553974808 | 8:143,381,873 | G/A | — | uncertain significance |
| rs372811762 | 8:143,381,879 | G/A | — | uncertain significance |
| rs560801617 | 8:143,381,911 | G/A | — | uncertain significance |
| rs532627645 | 8:143,381,992 | G/A | — | uncertain significance |
| rs373787442 | 8:143,395,764 | G/A | — | uncertain significance |
| rs777131187 | 8:143,395,765 | C/G | — | uncertain significance |
| rs751194559 | 8:143,396,372 | C/T | — | uncertain significance |
| rs779995622 | 8:143,396,383 | C/G | — | uncertain significance |
| rs751770922 | 8:143,396,389 | A/C | — | uncertain significance |
| rs761506216 | 8:143,396,420 | C/G | — | uncertain significance |
| rs756481116 | 8:143,396,429 | G/A | — | uncertain significance |
| rs372730805 | 8:143,396,432 | G/A | — | uncertain significance |
| rs62000450 | 8:143,396,446 | T/C | — | uncertain significance |
| rs769499748 | 8:143,396,447 | G/T | — | uncertain significance |
| rs566616065 | 8:143,399,906 | G/A | — | uncertain significance |
| rs759948818 | 8:143,399,910 | A/G | — | uncertain significance |
| rs527712157 | 8:143,399,914 | G/C | — | uncertain significance |
| rs754819424 | 8:143,399,936 | T/C | — | uncertain significance |
| rs144275934 | 8:143,399,953 | G/T | — | uncertain significance |
| rs190980494 | 8:143,412,313 | C/T | — | uncertain significance |
| rs573183661 | 8:143,413,138 | T/C | — | likely benign |
| rs147034875 | 8:143,413,143 | C/T | — | likely benign |
| rs2537824367 | 8:143,413,163 | C/T | — | uncertain significance |
| rs116253215 | 8:143,425,331 | G/A | — | benign |
| rs1833000406 | 8:143,425,394 | C/G | — | uncertain significance |
| rs775513022 | 8:143,425,471 | C/T | — | uncertain significance |
| rs759656596 | 8:143,425,485 | C/T | — | uncertain significance |
| rs375592742 | 8:143,425,489 | C/T | — | uncertain significance |
| rs144961640 | 8:143,425,506 | C/T | — | likely benign |
| rs778456613 | 8:143,425,507 | G/A | — | uncertain significance |
| rs142035138 | 8:143,425,536 | C/T | — | uncertain significance |
| rs146344045 | 8:143,425,539 | C/T | — | uncertain significance |
| rs577429987 | 8:143,425,596 | C/T | — | uncertain significance |
| rs555325950 | 8:143,425,597 | G/A | — | uncertain significance |
| rs370990303 | 8:143,425,606 | C/T | — | uncertain significance |
| rs1366238155 | 8:143,425,656 | T/C | — | uncertain significance |
| rs374263876 | 8:143,425,683 | G/A | — | uncertain significance |
| rs556972748 | 8:143,425,714 | G/A | — | uncertain significance |
| rs2538110925 | 8:143,425,722 | C/G | — | uncertain significance |
| rs199897318 | 8:143,425,738 | G/A | — | uncertain significance |
| rs116506890 | 8:143,425,770 | G/A | — | benign |
| rs755899900 | 8:143,425,771 | G/A | — | uncertain significance |
| rs747094810 | 8:143,425,807 | G/A | — | uncertain significance |
| rs199875184 | 8:143,425,822 | C/A | — | likely benign |
| rs762769281 | 8:143,425,828 | C/G | — | uncertain significance |
| rs774221161 | 8:143,427,106 | C/T | — | uncertain significance |
| rs147772559 | 8:143,427,128 | T/C | — | uncertain significance |
| rs370961209 | 8:143,427,133 | G/A | — | uncertain significance |
| rs1362644141 | 8:143,427,163 | T/C | — | uncertain significance |
| rs143680041 | 8:143,427,179 | G/A | — | uncertain significance |
| rs374842925 | 8:143,436,015 | T/C | — | uncertain significance |
| rs145679911 | 8:143,436,031 | C/T | — | uncertain significance |
| rs189103533 | 8:143,436,063 | C/A | — | uncertain significance |
| rs557067615 | 8:143,436,064 | G/A | — | uncertain significance |
| rs751858828 | 8:143,436,067 | C/T | — | uncertain significance |
| rs79047732 | 8:143,468,929 | T/A | intron variant | — |
| rs79053694 | 8:143,480,311 | C/T | upstream gene variant | — |
| rs59366013 | 8:143,483,603 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.