SV2C
synaptic vesicle glycoprotein 2C
Summary
Predicted to enable transmembrane transporter activity. Predicted to be involved in several processes, including chemical synaptic transmission; neurotransmitter transport; and regulation of synaptic vesicle exocytosis. Predicted to be located in plasma membrane and synaptic vesicle. Predicted to be active in dopaminergic synapse and synaptic vesicle membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs114098204 | 5:75,205,782 | G/A | upstream gene variant | — |
| rs72771940 | 5:75,271,632 | T/G | intergenic variant | — |
| rs116284526 | 5:75,346,805 | C/A | intergenic variant | — |
| rs777282920 | 5:75,427,606 | C/T | — | likely benign |
| rs771997327 | 5:75,427,663 | G/A | — | uncertain significance |
| rs761553818 | 5:75,427,692 | T/A | — | uncertain significance |
| rs1336599961 | 5:75,427,720 | T/C | — | uncertain significance |
| rs749242644 | 5:75,427,777 | G/A | — | uncertain significance |
| rs1199810418 | 5:75,427,859 | G/A | — | uncertain significance |
| rs146415005 | 5:75,427,880 | C/T | — | uncertain significance |
| rs10070440 | 5:75,427,935 | A/G | — | benign |
| rs562854902 | 5:75,427,936 | C/T | — | likely benign |
| rs528331991 | 5:75,428,044 | G/A | — | uncertain significance |
| rs73130289 | 5:75,428,070 | C/T | — | benign |
| rs143178564 | 5:75,428,074 | G/A | — | likely benign |
| rs774819373 | 5:75,428,089 | G/A | — | uncertain significance |
| rs2531192108 | 5:75,428,124 | C/T | — | likely benign |
| rs1748928801 | 5:75,428,147 | G/C | — | uncertain significance |
| rs182655756 | 5:75,428,164 | G/A | — | benign |
| rs6453204 | 5:75,439,200 | A/G | intron variant | — |
| rs13189798 | 5:75,487,251 | C/A | intron variant | — |
| rs2531330410 | 5:75,490,759 | T/A | — | uncertain significance |
| rs2531330590 | 5:75,490,792 | G/A | — | uncertain significance |
| rs2531330960 | 5:75,490,876 | T/C | — | uncertain significance |
| rs4704296 | 5:75,502,410 | G/C | intron variant | — |
| rs749975877 | 5:75,505,563 | T/C | — | uncertain significance |
| rs13153247 | 5:75,505,614 | G/A | — | uncertain significance |
| rs368119717 | 5:75,505,675 | C/T | — | likely benign |
| rs2531360899 | 5:75,505,677 | C/T | — | uncertain significance |
| rs757609434 | 5:75,505,697 | A/G | — | uncertain significance |
| rs372729641 | 5:75,505,705 | G/A | — | likely benign |
| rs772294806 | 5:75,541,988 | A/T | — | — |
| rs547353809 | 5:75,563,535 | G/A | — | — |
| rs4496693 | 5:75,576,729 | T/A | — | — |
| rs6453213 | 5:75,579,518 | A/G | regulatory region variant | — |
| rs7730153 | 5:75,579,762 | G/A | regulatory region variant | — |
| rs13174383 | 5:75,580,416 | T/G | downstream gene variant | — |
| rs776428022 | 5:75,581,034 | G/C | — | uncertain significance |
| rs149463986 | 5:75,581,068 | C/T | — | likely benign |
| rs775165202 | 5:75,581,107 | G/A | — | uncertain significance |
| rs370282974 | 5:75,587,046 | G/A | — | uncertain significance |
| rs770526223 | 5:75,587,139 | C/T | — | uncertain significance |
| rs190593094 | 5:75,587,140 | G/A | — | benign |
| rs200154327 | 5:75,587,145 | G/A | — | uncertain significance |
| rs769028669 | 5:75,587,605 | T/A | — | uncertain significance |
| rs1352239915 | 5:75,591,617 | C/A | — | uncertain significance |
| rs755581046 | 5:75,591,623 | G/T | — | uncertain significance |
| rs2270927 | 5:75,591,710 | C/G | — | benign |
| rs201019699 | 5:75,594,624 | T/C | — | uncertain significance |
| rs778645466 | 5:75,594,629 | G/A | — | uncertain significance |
| rs31244 | 5:75,594,743 | A/G | — | benign |
| rs768196341 | 5:75,596,565 | T/C | — | uncertain significance |
| rs373236256 | 5:75,596,577 | G/A | — | uncertain significance |
| rs781226822 | 5:75,596,617 | C/T | — | uncertain significance |
| rs113489031 | 5:75,596,618 | G/A | — | benign |
| rs2531561387 | 5:75,596,623 | G/A | — | uncertain significance |
| rs748973204 | 5:75,596,650 | G/T | — | uncertain significance |
| rs768222996 | 5:75,596,651 | T/C | — | likely benign |
| rs375494365 | 5:75,596,655 | T/C | — | uncertain significance |
| rs2531561654 | 5:75,596,674 | A/G | — | uncertain significance |
| rs756743267 | 5:75,596,742 | C/T | — | uncertain significance |
| rs772962809 | 5:75,597,213 | G/A | — | uncertain significance |
| rs781697227 | 5:75,597,278 | G/A | — | uncertain significance |
| rs374677576 | 5:75,597,296 | G/T | — | likely benign |
| rs200769447 | 5:75,597,301 | A/G | — | uncertain significance |
| rs372341328 | 5:75,597,361 | C/T | — | uncertain significance |
| rs202233851 | 5:75,597,367 | G/A | — | uncertain significance |
| rs246815 | 5:75,599,176 | G/C | intron variant | — |
| rs246814 | 5:75,599,208 | C/T | intron variant | — |
| rs554653198 | 5:75,621,215 | C/T | — | uncertain significance |
| rs183714782 | 5:75,621,216 | G/A | — | likely benign |
| rs572553728 | 5:75,621,313 | G/A | — | uncertain significance |
| rs1432614415 | 5:75,621,329 | T/C | — | uncertain significance |
| rs3733860 | 5:75,622,814 | C/A | regulatory region variant | — |
| rs73117804 | 5:75,649,280 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.