SYTL3
synaptotagmin like 3
Summary
The protein encoded by this gene belongs to a family of peripheral membrane proteins that play a role in vesicular trafficking. This protein binds phospholipids in the presence of calcium ions. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201251694 | 6:159,084,320 | T/A | — | uncertain significance |
| rs764479125 | 6:159,084,348 | G/C | — | uncertain significance |
| rs762716551 | 6:159,084,409 | C/T | — | uncertain significance |
| rs140236569 | 6:159,086,507 | C/T | — | uncertain significance |
| rs1359502238 | 6:159,086,516 | A/G | — | uncertain significance |
| rs750075730 | 6:159,086,546 | G/A | — | uncertain significance |
| rs139337109 | 6:159,086,573 | G/A | — | uncertain significance |
| rs569567936 | 6:159,086,582 | C/T | — | uncertain significance |
| rs751441226 | 6:159,086,638 | G/C | — | uncertain significance |
| rs572777768 | 6:159,115,383 | A/G | — | — |
| rs757933847 | 6:159,129,377 | C/T | — | uncertain significance |
| rs931333 | 6:159,136,652 | C/T | regulatory region variant | — |
| rs2483495609 | 6:159,139,134 | A/G | — | uncertain significance |
| rs912118408 | 6:159,139,139 | G/A | — | uncertain significance |
| rs1001349400 | 6:159,139,224 | C/T | — | uncertain significance |
| rs772269862 | 6:159,146,586 | T/C | — | likely benign |
| rs201406240 | 6:159,146,635 | C/T | — | uncertain significance |
| rs146498881 | 6:159,146,659 | G/T | — | uncertain significance |
| rs2484002201 | 6:159,166,530 | G/A | — | likely benign |
| rs557180630 | 6:159,166,597 | T/C | — | uncertain significance |
| rs199560956 | 6:159,166,606 | G/T | — | uncertain significance |
| rs202000849 | 6:159,178,274 | G/A | — | uncertain significance |
| rs2484240847 | 6:159,178,292 | T/C | — | uncertain significance |
| rs141770650 | 6:159,178,391 | G/A | — | uncertain significance |
| rs184979069 | 6:159,181,673 | C/T | — | uncertain significance |
| rs749669847 | 6:159,181,693 | G/A | — | uncertain significance |
| rs117895837 | 6:159,181,740 | C/T | — | likely benign |
| rs777596209 | 6:159,181,747 | C/T | — | uncertain significance |
| rs148493778 | 6:159,183,170 | C/T | — | uncertain significance |
| rs2171209 | 6:159,183,562 | T/C | downstream gene variant | — |
| rs752579130 | 6:159,184,407 | A/C | — | uncertain significance |
| rs746030221 | 6:159,184,446 | C/G | — | uncertain significance |
| rs774693205 | 6:159,184,478 | G/T | — | uncertain significance |
| rs369908524 | 6:159,184,488 | A/C | — | uncertain significance |
| rs758443239 | 6:159,185,581 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.