PNLIPRP1
pancreatic lipase related protein 1
Summary
Predicted to enable calcium ion binding activity; lipoprotein lipase activity; and phospholipase A1 activity. Predicted to be involved in several processes, including cholesterol homeostasis; high-density lipoprotein particle remodeling; and triglyceride catabolic process. Predicted to be located in extracellular region. Biomarker of prostate cancer. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs782733636 | 10:118,351,304 | A/G | — | uncertain significance |
| rs782526462 | 10:118,351,309 | G/C | — | uncertain significance |
| rs782433696 | 10:118,351,337 | G/A | — | uncertain significance |
| rs782704920 | 10:118,351,390 | G/A | — | uncertain significance |
| rs115887041 | 10:118,351,397 | G/A | — | uncertain significance |
| rs141478509 | 10:118,351,992 | G/A | — | uncertain significance |
| rs782149122 | 10:118,352,029 | G/C | — | uncertain significance |
| rs2493098443 | 10:118,352,043 | A/G | — | uncertain significance |
| rs1847658206 | 10:118,352,048 | T/C | — | uncertain significance |
| rs193113580 | 10:118,352,294 | T/C | intron variant | — |
| rs184338868 | 10:118,353,288 | G/C | intron variant | — |
| rs186836921 | 10:118,353,584 | T/C | intron variant | — |
| rs12258286 | 10:118,353,830 | G/T | intron variant | — |
| rs782300185 | 10:118,354,251 | G/A | — | likely benign |
| rs998634455 | 10:118,354,342 | G/T | — | uncertain significance |
| rs2493106629 | 10:118,355,730 | A/G | — | uncertain significance |
| rs200174051 | 10:118,355,744 | C/T | — | uncertain significance |
| rs140020062 | 10:118,355,745 | C/G | — | uncertain significance |
| rs141916863 | 10:118,355,747 | T/G | — | uncertain significance |
| rs139392611 | 10:118,355,780 | G/C | — | uncertain significance |
| rs782722033 | 10:118,355,786 | G/A | — | uncertain significance |
| rs1847734709 | 10:118,355,806 | C/G | — | uncertain significance |
| rs549029336 | 10:118,356,820 | C/T | — | — |
| rs782187986 | 10:118,357,378 | G/A | — | uncertain significance |
| rs116567197 | 10:118,357,388 | G/A | — | uncertain significance |
| rs782804332 | 10:118,357,430 | C/T | — | uncertain significance |
| rs1758029905 | 10:118,359,559 | G/A | — | uncertain significance |
| rs199754358 | 10:118,359,564 | C/T | — | uncertain significance |
| rs376297190 | 10:118,360,597 | C/T | — | uncertain significance |
| rs568726613 | 10:118,360,648 | C/T | — | uncertain significance |
| rs369604475 | 10:118,360,710 | G/A | — | likely benign |
| rs547496564 | 10:118,361,438 | A/G | — | — |
| rs45604841 | 10:118,363,528 | C/T | intron variant | — |
| rs781860088 | 10:118,363,560 | C/A | — | uncertain significance |
| rs1847895639 | 10:118,363,596 | T/A | — | uncertain significance |
| rs1554865215 | 10:118,363,609 | G/C | — | uncertain significance |
| rs116610181 | 10:118,363,612 | T/C | synonymous variant | — |
| rs60134363 | 10:118,364,037 | C/A | — | — |
| rs372162169 | 10:118,364,963 | T/C | — | uncertain significance |
| rs1198885132 | 10:118,365,019 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.