PROSER1
proline and serine rich 1
Summary
This gene encodes a conserved protein containing proline and serine rich regions. These regions may be important in protein-protein interactions. [provided by RefSeq, Aug 2012]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs774294238 | 13:39,585,524 | A/G | — | uncertain significance |
| rs73169461 | 13:39,585,591 | A/C | — | uncertain significance |
| rs2541589070 | 13:39,586,252 | T/G | — | uncertain significance |
| rs138892103 | 13:39,586,270 | A/C | — | uncertain significance |
| rs187958429 | 13:39,586,847 | C/T | — | uncertain significance |
| rs17058955 | 13:39,586,850 | A/T | — | benign |
| rs761563804 | 13:39,586,925 | G/A | — | uncertain significance |
| rs767070879 | 13:39,586,926 | T/C | — | likely benign |
| rs17058957 | 13:39,586,977 | G/A | — | benign |
| rs147842168 | 13:39,586,984 | G/A | — | uncertain significance |
| rs754985997 | 13:39,586,997 | T/C | — | uncertain significance |
| rs369279863 | 13:39,587,026 | T/C | — | uncertain significance |
| rs767629281 | 13:39,587,078 | G/C | — | uncertain significance |
| rs79004953 | 13:39,587,123 | G/T | — | uncertain significance |
| rs1566021375 | 13:39,587,138 | G/A | — | uncertain significance |
| rs1218856425 | 13:39,587,150 | C/G | — | uncertain significance |
| rs770767864 | 13:39,587,158 | G/A | — | uncertain significance |
| rs775781861 | 13:39,587,195 | C/T | — | uncertain significance |
| rs1308635398 | 13:39,587,239 | G/A | — | uncertain significance |
| rs369340510 | 13:39,587,285 | A/T | — | uncertain significance |
| rs1354554971 | 13:39,587,391 | C/G | — | uncertain significance |
| rs765393708 | 13:39,587,468 | G/A | — | uncertain significance |
| rs778728502 | 13:39,587,528 | C/A | — | uncertain significance |
| rs745947407 | 13:39,587,545 | G/A | — | uncertain significance |
| rs774465997 | 13:39,587,591 | C/T | — | uncertain significance |
| rs753324795 | 13:39,587,605 | G/A | — | uncertain significance |
| rs201086093 | 13:39,587,642 | G/A | — | uncertain significance |
| rs749378496 | 13:39,587,659 | G/A | — | uncertain significance |
| rs137855398 | 13:39,587,720 | C/T | — | likely benign |
| rs368668535 | 13:39,587,757 | G/A | — | likely benign |
| rs35453341 | 13:39,587,763 | T/C | — | benign |
| rs546645213 | 13:39,587,824 | G/A | — | uncertain significance |
| rs2541594485 | 13:39,587,962 | A/C | — | uncertain significance |
| rs201650265 | 13:39,588,002 | C/T | — | uncertain significance |
| rs1869845498 | 13:39,588,008 | G/A | — | uncertain significance |
| rs1377247455 | 13:39,588,049 | G/T | — | uncertain significance |
| rs369951334 | 13:39,588,079 | G/A | — | uncertain significance |
| rs747675048 | 13:39,588,179 | T/C | — | uncertain significance |
| rs1357375420 | 13:39,588,229 | C/T | — | uncertain significance |
| rs141429117 | 13:39,588,233 | G/A | — | uncertain significance |
| rs1190460158 | 13:39,588,241 | C/G | — | uncertain significance |
| rs1442502560 | 13:39,588,293 | C/T | — | uncertain significance |
| rs1437816940 | 13:39,588,317 | C/G | — | uncertain significance |
| rs145804132 | 13:39,588,356 | C/T | — | uncertain significance |
| rs138649285 | 13:39,588,379 | A/G | — | uncertain significance |
| rs750422319 | 13:39,588,526 | G/A | — | uncertain significance |
| rs769021056 | 13:39,588,542 | C/T | — | uncertain significance |
| rs141612774 | 13:39,588,565 | G/A | — | uncertain significance |
| rs749940728 | 13:39,588,578 | G/A | — | uncertain significance |
| rs778168067 | 13:39,596,490 | G/C | — | uncertain significance |
| rs570957169 | 13:39,596,516 | G/A | — | uncertain significance |
| rs773038908 | 13:39,597,212 | C/T | — | uncertain significance |
| rs190094996 | 13:39,597,245 | T/C | — | uncertain significance |
| rs752907143 | 13:39,597,254 | T/C | — | uncertain significance |
| rs758697111 | 13:39,597,258 | T/C | — | uncertain significance |
| rs201397537 | 13:39,598,627 | G/T | — | uncertain significance |
| rs746137326 | 13:39,602,450 | T/G | — | uncertain significance |
| rs780153404 | 13:39,603,469 | T/C | — | uncertain significance |
| rs749523136 | 13:39,603,473 | G/T | — | uncertain significance |
| rs376921057 | 13:39,603,478 | T/C | — | uncertain significance |
| rs750422260 | 13:39,603,484 | A/G | — | uncertain significance |
| rs1870844441 | 13:39,605,717 | T/C | — | uncertain significance |
| rs2541621689 | 13:39,605,755 | A/G | — | uncertain significance |
| rs41286947 | 13:39,613,641 | A/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.