SVOPL
SVOP like
Summary
The protein encoded by this gene is thought to be a member of solute carrier family 22, which includes transmembrane proteins that transport toxins and drugs from the body. This gene is a paralog of the SVOP gene that encodes synaptic vesicle 2-related protein. [provided by RefSeq, Sep 2016]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs141292389 | 7:138,279,366 | G/T | — | uncertain significance |
| rs781683701 | 7:138,281,163 | T/C | — | uncertain significance |
| rs145071968 | 7:138,281,172 | C/G | — | uncertain significance |
| rs141398137 | 7:138,281,188 | T/C | — | uncertain significance |
| rs775097536 | 7:138,281,196 | G/A | — | uncertain significance |
| rs142898787 | 7:138,281,268 | A/G | — | uncertain significance |
| rs199794073 | 7:138,305,822 | A/T | — | uncertain significance |
| rs1799545185 | 7:138,305,847 | C/T | — | uncertain significance |
| rs564267291 | 7:138,305,862 | G/A | — | uncertain significance |
| rs765749268 | 7:138,305,867 | G/T | — | uncertain significance |
| rs745563010 | 7:138,310,734 | C/T | — | likely benign |
| rs758979003 | 7:138,312,134 | G/A | — | uncertain significance |
| rs774616578 | 7:138,312,165 | G/A | — | uncertain significance |
| rs773196860 | 7:138,312,191 | A/G | — | uncertain significance |
| rs369769509 | 7:138,312,915 | C/T | — | uncertain significance |
| rs1563101402 | 7:138,312,975 | G/A | — | uncertain significance |
| rs1472173621 | 7:138,312,977 | C/T | — | uncertain significance |
| rs200942722 | 7:138,312,987 | C/T | — | likely benign |
| rs562489887 | 7:138,312,996 | C/A | — | uncertain significance |
| rs200115398 | 7:138,313,002 | C/A | — | uncertain significance |
| rs201768743 | 7:138,313,016 | G/A | — | uncertain significance |
| rs142884011 | 7:138,313,071 | C/T | — | uncertain significance |
| rs374304743 | 7:138,313,077 | T/A | — | uncertain significance |
| rs745619788 | 7:138,313,088 | T/C | — | uncertain significance |
| rs149009334 | 7:138,314,822 | G/A | — | uncertain significance |
| rs199975503 | 7:138,314,823 | T/G | — | uncertain significance |
| rs1057288113 | 7:138,329,470 | G/T | — | uncertain significance |
| rs571787686 | 7:138,329,491 | G/A | — | uncertain significance |
| rs369684225 | 7:138,329,520 | C/T | — | likely benign |
| rs144481050 | 7:138,329,571 | C/A | — | uncertain significance |
| rs79848686 | 7:138,329,572 | G/A | — | benign |
| rs199580070 | 7:138,329,582 | A/G | — | likely benign |
| rs140188327 | 7:138,333,769 | G/A | — | benign |
| rs1801284650 | 7:138,333,778 | G/C | — | uncertain significance |
| rs150440671 | 7:138,333,819 | C/T | — | benign |
| rs1801292938 | 7:138,333,866 | C/A | — | uncertain significance |
| rs145183727 | 7:138,333,869 | G/A | — | uncertain significance |
| rs566342063 | 7:138,341,209 | A/G | — | uncertain significance |
| rs117871806 | 7:138,341,219 | G/A | — | likely benign |
| rs138174501 | 7:138,341,227 | G/A | — | uncertain significance |
| rs537537354 | 7:138,341,228 | T/C | — | uncertain significance |
| rs778275252 | 7:138,344,649 | G/A | — | uncertain significance |
| rs757982706 | 7:138,344,672 | G/A | — | uncertain significance |
| rs558959764 | 7:138,356,765 | G/A | — | uncertain significance |
| rs2485684464 | 7:138,356,781 | C/T | — | uncertain significance |
| rs779169354 | 7:138,356,810 | C/T | — | uncertain significance |
| rs191061647 | 7:138,356,811 | G/A | — | uncertain significance |
| rs2485697512 | 7:138,363,201 | A/T | — | uncertain significance |
| rs371850845 | 7:138,363,205 | G/T | — | uncertain significance |
| rs2485697528 | 7:138,363,207 | G/T | — | uncertain significance |
| rs2485697601 | 7:138,363,237 | T/C | — | uncertain significance |
| rs1802627341 | 7:138,363,263 | C/A | — | uncertain significance |
| rs567055062 | 7:138,371,400 | T/C | — | — |
| rs296915 | 7:138,376,658 | T/G | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.