SYT16
synaptotagmin 16
Summary
Predicted to enable phospholipid binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2784505 | 14:62,432,013 | A/G | regulatory region variant | — |
| rs779841902 | 14:62,462,831 | G/A | — | uncertain significance |
| rs781569552 | 14:62,462,866 | C/G | — | uncertain significance |
| rs2503070504 | 14:62,462,969 | C/G | — | uncertain significance |
| rs201921515 | 14:62,462,981 | A/C | — | uncertain significance |
| rs2052769508 | 14:62,463,081 | A/G | — | uncertain significance |
| rs564353410 | 14:62,463,111 | A/G | — | likely benign |
| rs376295336 | 14:62,463,155 | A/C | — | uncertain significance |
| rs1299416149 | 14:62,463,233 | T/G | — | uncertain significance |
| rs192369127 | 14:62,463,257 | C/A | — | uncertain significance |
| rs6573416 | 14:62,518,348 | C/G | intron variant | — |
| rs748603841 | 14:62,536,350 | T/G | — | uncertain significance |
| rs2503488153 | 14:62,536,380 | A/G | — | uncertain significance |
| rs201464926 | 14:62,536,408 | G/A | — | uncertain significance |
| rs368612700 | 14:62,536,423 | G/A | — | uncertain significance |
| rs190756776 | 14:62,536,483 | G/A | — | likely benign |
| rs9323382 | 14:62,537,047 | A/G | intron variant | — |
| rs372127808 | 14:62,541,873 | C/T | — | uncertain significance |
| rs201271787 | 14:62,541,876 | C/T | — | uncertain significance |
| rs201294056 | 14:62,541,877 | G/A | — | uncertain significance |
| rs1464588623 | 14:62,541,898 | A/G | — | uncertain significance |
| rs760243988 | 14:62,541,916 | T/C | — | uncertain significance |
| rs2503522841 | 14:62,541,921 | G/C | — | uncertain significance |
| rs1012505008 | 14:62,541,939 | T/C | — | uncertain significance |
| rs200718503 | 14:62,541,943 | A/G | — | uncertain significance |
| rs775256228 | 14:62,542,008 | C/T | — | uncertain significance |
| rs8006191 | 14:62,546,570 | T/G | — | — |
| rs1486012042 | 14:62,547,580 | C/A | — | uncertain significance |
| rs200117132 | 14:62,547,645 | G/A | — | uncertain significance |
| rs769729683 | 14:62,547,693 | G/C | — | uncertain significance |
| rs1289497787 | 14:62,547,709 | G/T | — | uncertain significance |
| rs753437177 | 14:62,547,844 | C/T | — | uncertain significance |
| rs757964384 | 14:62,547,858 | C/T | — | uncertain significance |
| rs775455829 | 14:62,547,889 | C/T | — | uncertain significance |
| rs376404574 | 14:62,547,891 | C/G | — | uncertain significance |
| rs2503570684 | 14:62,547,913 | A/G | — | uncertain significance |
| rs4902100 | 14:62,549,819 | G/A | upstream gene variant | — |
| rs368479627 | 14:62,550,972 | C/T | — | uncertain significance |
| rs764011634 | 14:62,567,112 | A/G | — | uncertain significance |
| rs772362826 | 14:62,567,181 | G/A | — | uncertain significance |
| rs760675924 | 14:62,567,184 | G/A | — | uncertain significance |
| rs776763293 | 14:62,567,196 | A/G | — | uncertain significance |
| rs780876820 | 14:62,567,270 | G/A | — | likely benign |
| rs769941155 | 14:62,567,336 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.