SPOCK1
SPARC (osteonectin), cwcv and kazal like domains proteoglycan 1
Summary
This gene encodes the protein core of a seminal plasma proteoglycan containing chondroitin- and heparan-sulfate chains. The protein's function is unknown, although similarity to thyropin-type cysteine protease-inhibitors suggests its function may be related to protease inhibition. [provided by RefSeq, Jul 2008]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs750609373 | 5:136,314,422 | C/G | — | uncertain significance |
| rs1750884060 | 5:136,324,172 | G/C | — | uncertain significance |
| rs762483512 | 5:136,324,192 | G/T | — | uncertain significance |
| rs145057831 | 5:136,324,207 | C/T | — | uncertain significance |
| rs1220306555 | 5:136,324,223 | G/T | — | likely benign |
| rs1364549281 | 5:136,324,255 | G/C | — | uncertain significance |
| rs376099963 | 5:136,324,285 | T/C | — | uncertain significance |
| rs570322584 | 5:136,324,318 | T/C | — | uncertain significance |
| rs144777015 | 5:136,328,212 | T/C | — | uncertain significance |
| rs1158891066 | 5:136,328,241 | C/A | — | uncertain significance |
| rs201506391 | 5:136,328,269 | G/A | — | uncertain significance |
| rs17170899 | 5:136,376,050 | C/T | intron variant | — |
| rs2189597 | 5:136,387,259 | C/G | intron variant | — |
| rs1752536855 | 5:136,403,428 | G/C | — | uncertain significance |
| rs201888683 | 5:136,403,470 | G/T | — | uncertain significance |
| rs139465331 | 5:136,403,476 | C/T | — | likely benign |
| rs751193264 | 5:136,403,485 | T/C | — | uncertain significance |
| rs200904423 | 5:136,403,506 | A/G | — | uncertain significance |
| rs11953059 | 5:136,416,216 | T/C | intron variant | — |
| rs17600115 | 5:136,420,952 | G/A | intron variant | — |
| rs13357391 | 5:136,441,082 | T/C | intron variant | — |
| rs1859345 | 5:136,447,420 | T/G | — | — |
| rs149726803 | 5:136,448,170 | T/C | — | uncertain significance |
| rs774330060 | 5:136,448,177 | C/T | — | uncertain significance |
| rs148446530 | 5:136,448,179 | G/A | — | uncertain significance |
| rs1490313055 | 5:136,448,185 | G/T | — | uncertain significance |
| rs1205221878 | 5:136,448,200 | A/C | — | uncertain significance |
| rs144155642 | 5:136,448,205 | C/T | — | likely benign |
| rs146503135 | 5:136,448,206 | G/A | — | uncertain significance |
| rs199506446 | 5:136,476,288 | G/A | — | uncertain significance |
| rs151283855 | 5:136,476,303 | C/T | — | uncertain significance |
| rs587777311 | 5:136,476,377 | T/A | — | uncertain significance |
| rs1369127 | 5:136,543,488 | A/C | intron variant | — |
| rs13189692 | 5:136,569,448 | G/T | — | — |
| rs13163306 | 5:136,571,959 | G/T | — | — |
| rs13187474 | 5:136,581,450 | C/A | — | — |
| rs764295606 | 5:136,602,727 | G/C | — | uncertain significance |
| rs2905552 | 5:136,629,284 | G/C | regulatory region variant | — |
| rs35215630 | 5:136,765,039 | C/T | intron variant | — |
| rs116542708 | 5:136,771,052 | A/G | intron variant | — |
| rs10214086 | 5:136,783,945 | A/C | — | — |
| rs533419807 | 5:136,802,524 | G/T | — | — |
| rs145696269 | 5:136,803,188 | T/C | intron variant | — |
| rs111393448 | 5:136,834,138 | C/T | — | benign |
| rs201111918 | 5:136,834,139 | T/C | — | uncertain significance |
| rs1351576062 | 5:136,834,141 | C/T | — | uncertain significance |
| rs200001053 | 5:136,834,142 | C/G | — | uncertain significance |
| rs1247765993 | 5:136,834,143 | G/A | — | likely benign |
| rs1321580135 | 5:136,834,177 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.