SERPINA11
serpin family A member 11
Summary
Predicted to enable serine-type endopeptidase inhibitor activity. Predicted to be located in extracellular region. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs148974258 | 14:94,908,476 | T/C | downstream gene variant | — |
| rs150820756 | 14:94,908,958 | G/T | — | uncertain significance |
| rs1249999049 | 14:94,908,963 | C/A | — | uncertain significance |
| rs144603054 | 14:94,909,024 | C/T | synonymous variant | — |
| rs115765596 | 14:94,909,051 | C/A | — | uncertain significance |
| rs1898366545 | 14:94,909,095 | C/T | — | uncertain significance |
| rs770972131 | 14:94,909,098 | C/T | — | uncertain significance |
| rs763826276 | 14:94,909,106 | G/C | — | uncertain significance |
| rs202035957 | 14:94,909,479 | T/C | — | uncertain significance |
| rs747412188 | 14:94,909,503 | A/G | — | uncertain significance |
| rs115771804 | 14:94,912,704 | T/C | — | benign |
| rs776327381 | 14:94,912,743 | G/A | — | uncertain significance |
| rs576980680 | 14:94,912,753 | G/A | — | uncertain significance |
| rs563316230 | 14:94,912,764 | G/A | — | uncertain significance |
| rs143678178 | 14:94,912,798 | C/T | — | uncertain significance |
| rs1266779884 | 14:94,912,861 | C/T | — | likely benign |
| rs776902350 | 14:94,912,897 | C/T | — | uncertain significance |
| rs775643756 | 14:94,912,913 | G/T | — | likely pathogenic |
| rs114788552 | 14:94,912,918 | G/A | — | uncertain significance |
| rs914076396 | 14:94,912,930 | G/A | — | uncertain significance |
| rs17090881 | 14:94,913,209 | C/A | intron variant | — |
| rs148495961 | 14:94,914,468 | C/T | — | uncertain significance |
| rs760533993 | 14:94,914,486 | T/C | — | uncertain significance |
| rs1296032219 | 14:94,914,493 | G/A | — | uncertain significance |
| rs756265934 | 14:94,914,523 | G/A | — | uncertain significance |
| rs201110965 | 14:94,914,535 | C/T | — | uncertain significance |
| rs768060913 | 14:94,914,576 | T/C | — | uncertain significance |
| rs372977604 | 14:94,914,637 | C/G | — | uncertain significance |
| rs61738925 | 14:94,914,667 | G/A | missense variant | — |
| rs774059044 | 14:94,914,753 | C/T | — | likely benign |
| rs1243656394 | 14:94,914,814 | G/T | — | uncertain significance |
| rs368570129 | 14:94,914,841 | C/G | — | uncertain significance |
| rs2504893071 | 14:94,914,856 | G/T | — | uncertain significance |
| rs1286050545 | 14:94,914,873 | A/G | — | uncertain significance |
| rs776025031 | 14:94,914,901 | C/T | — | uncertain significance |
| rs751625781 | 14:94,914,904 | G/A | — | uncertain significance |
| rs778640326 | 14:94,914,911 | T/A | — | likely benign |
| rs746333705 | 14:94,914,945 | T/C | — | likely benign |
| rs902711194 | 14:94,915,008 | G/T | — | uncertain significance |
| rs1460834021 | 14:94,915,009 | G/T | — | uncertain significance |
| rs200425882 | 14:94,915,048 | G/T | — | uncertain significance |
| rs55664577 | 14:94,915,836 | T/C | — | — |
| rs56026704 | 14:94,915,948 | T/G | — | — |
| rs187945070 | 14:94,916,140 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.