PRSS53
serine protease 53
Summary
Predicted to enable serine-type endopeptidase activity. Predicted to be involved in proteolysis. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2544095878 | 16:31,095,464 | G/A | — | uncertain significance |
| rs377498752 | 16:31,095,488 | C/T | — | uncertain significance |
| rs2544096124 | 16:31,095,494 | A/G | — | uncertain significance |
| rs145846447 | 16:31,095,544 | G/A | — | uncertain significance |
| rs757127573 | 16:31,095,587 | C/T | — | uncertain significance |
| rs989150303 | 16:31,095,602 | C/T | — | uncertain significance |
| rs534125608 | 16:31,095,619 | C/T | — | uncertain significance |
| rs571013204 | 16:31,095,643 | G/T | — | uncertain significance |
| rs1414445253 | 16:31,095,941 | C/T | — | uncertain significance |
| rs780868168 | 16:31,095,959 | C/T | — | likely benign |
| rs2544099305 | 16:31,095,979 | C/G | — | uncertain significance |
| rs773359736 | 16:31,096,118 | C/T | — | uncertain significance |
| rs7199949 | 16:31,096,164 | G/T | missense variant | — |
| rs2544101213 | 16:31,096,231 | C/A | — | uncertain significance |
| rs1351540994 | 16:31,096,245 | C/G | — | uncertain significance |
| rs1169290199 | 16:31,096,301 | G/A | — | uncertain significance |
| rs751441935 | 16:31,096,320 | C/T | — | uncertain significance |
| rs377232515 | 16:31,096,343 | C/T | — | uncertain significance |
| rs370867880 | 16:31,096,442 | G/A | — | likely benign |
| rs199760254 | 16:31,096,489 | A/G | — | uncertain significance |
| rs768600226 | 16:31,097,325 | G/C | — | uncertain significance |
| rs2544107339 | 16:31,097,446 | C/G | — | uncertain significance |
| rs753877424 | 16:31,097,466 | G/C | — | uncertain significance |
| rs375149743 | 16:31,097,474 | C/G | — | uncertain significance |
| rs780736067 | 16:31,097,495 | C/T | — | uncertain significance |
| rs368809497 | 16:31,097,670 | C/G | — | uncertain significance |
| rs376647266 | 16:31,097,671 | T/C | — | uncertain significance |
| rs748258706 | 16:31,097,762 | A/G | — | uncertain significance |
| rs766085215 | 16:31,097,771 | G/A | — | uncertain significance |
| rs374267853 | 16:31,097,782 | C/T | — | uncertain significance |
| rs201523648 | 16:31,097,788 | C/T | — | uncertain significance |
| rs374655723 | 16:31,097,803 | G/A | — | uncertain significance |
| rs200180874 | 16:31,097,957 | C/T | — | uncertain significance |
| rs779237002 | 16:31,098,062 | G/A | — | uncertain significance |
| rs559983068 | 16:31,098,166 | C/T | — | uncertain significance |
| rs1051052208 | 16:31,098,169 | T/G | — | uncertain significance |
| rs537071727 | 16:31,098,910 | C/T | — | uncertain significance |
| rs2544113890 | 16:31,098,972 | G/A | — | uncertain significance |
| rs573693329 | 16:31,098,991 | T/C | — | likely benign |
| rs11150606 | 16:31,099,011 | T/A | missense variant | — |
| rs17839568 | 16:31,099,783 | T/C | downstream gene variant | — |
| rs73530203 | 16:31,099,859 | G/A | downstream gene variant | — |
| rs2544118093 | 16:31,100,091 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.