PAMR1
peptidase domain containing associated with muscle regeneration 1
Summary
Predicted to enable calcium ion binding activity and 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 Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs763253267 | 11:35,453,925 | C/A | — | uncertain significance |
| rs950453184 | 11:35,454,026 | G/A | — | uncertain significance |
| rs201029324 | 11:35,454,046 | G/A | — | uncertain significance |
| rs143102071 | 11:35,454,061 | G/A | — | uncertain significance |
| rs774588409 | 11:35,454,142 | C/T | — | uncertain significance |
| rs138681708 | 11:35,454,165 | A/G | — | likely benign |
| rs199759649 | 11:35,454,214 | C/T | — | uncertain significance |
| rs368802780 | 11:35,454,215 | G/A | — | uncertain significance |
| rs200247903 | 11:35,454,313 | C/T | — | uncertain significance |
| rs773899087 | 11:35,454,346 | G/A | — | uncertain significance |
| rs752627585 | 11:35,454,355 | C/T | — | uncertain significance |
| rs370534974 | 11:35,454,356 | G/A | — | uncertain significance |
| rs138978009 | 11:35,456,085 | T/A | missense variant | — |
| rs767807537 | 11:35,456,100 | C/T | — | uncertain significance |
| rs1357540236 | 11:35,456,116 | A/C | — | uncertain significance |
| rs550753385 | 11:35,456,146 | T/C | — | likely benign |
| rs577038460 | 11:35,456,266 | C/T | — | uncertain significance |
| rs372889720 | 11:35,456,304 | C/T | — | uncertain significance |
| rs138210503 | 11:35,457,471 | C/T | — | uncertain significance |
| rs763793747 | 11:35,457,472 | G/A | — | uncertain significance |
| rs2498647833 | 11:35,457,498 | C/T | — | uncertain significance |
| rs777948907 | 11:35,457,522 | C/T | — | uncertain significance |
| rs142812833 | 11:35,457,607 | C/T | — | uncertain significance |
| rs377424823 | 11:35,457,655 | C/T | — | uncertain significance |
| rs1856122493 | 11:35,461,199 | A/T | — | uncertain significance |
| rs770476180 | 11:35,463,075 | G/C | — | uncertain significance |
| rs2498662517 | 11:35,463,082 | C/A | — | uncertain significance |
| rs141335779 | 11:35,463,134 | C/T | — | uncertain significance |
| rs149018193 | 11:35,463,155 | G/A | — | uncertain significance |
| rs760914031 | 11:35,463,199 | T/C | — | uncertain significance |
| rs779555385 | 11:35,463,215 | G/T | — | uncertain significance |
| rs192184018 | 11:35,465,944 | G/A | intron variant | — |
| rs7129975 | 11:35,483,521 | A/C | intron variant | — |
| rs185501879 | 11:35,487,445 | T/C | intron variant | — |
| rs369548670 | 11:35,489,560 | C/T | — | likely benign |
| rs756264095 | 11:35,492,179 | C/T | — | uncertain significance |
| rs771251137 | 11:35,492,182 | C/T | — | uncertain significance |
| rs150779939 | 11:35,492,230 | C/G | — | uncertain significance |
| rs776344621 | 11:35,492,254 | G/A | — | uncertain significance |
| rs139790960 | 11:35,492,308 | G/A | — | uncertain significance |
| rs747701550 | 11:35,492,319 | T/C | — | uncertain significance |
| rs1856841556 | 11:35,492,341 | C/A | — | uncertain significance |
| rs1996369 | 11:35,495,441 | C/A | — | — |
| rs117968051 | 11:35,496,184 | T/C | — | uncertain significance |
| rs10768140 | 11:35,510,907 | T/G | intron variant | — |
| rs143549343 | 11:35,513,706 | T/G | — | uncertain significance |
| rs184827720 | 11:35,515,296 | C/T | intron variant | — |
| rs577966398 | 11:35,515,734 | C/T | — | uncertain significance |
| rs1356752489 | 11:35,515,773 | T/C | — | uncertain significance |
| rs650950 | 11:35,539,269 | T/G | — | — |
| rs780818446 | 11:35,547,088 | G/C | — | uncertain significance |
| rs201455935 | 11:35,547,099 | G/C | — | uncertain significance |
| rs2494581429 | 11:35,547,120 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.