SERPINB3
serpin family B member 3
Summary
Enables cysteine-type endopeptidase inhibitor activity; protease binding activity; and virus receptor activity. Involved in several processes, including autocrine signaling; paracrine signaling; and regulation of protein metabolic process. Located in several cellular components, including cytoplasmic vesicle; cytosol; and extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1913472334 | 18:61,322,914 | A/G | — | uncertain significance |
| rs1435014101 | 18:61,322,920 | G/A | — | uncertain significance |
| rs141091024 | 18:61,322,943 | C/T | — | likely benign |
| rs1410761660 | 18:61,322,961 | G/A | — | uncertain significance |
| rs769288329 | 18:61,322,970 | C/T | — | uncertain significance |
| rs12953909 | 18:61,322,980 | C/T | — | benign |
| rs761063030 | 18:61,322,983 | C/T | — | uncertain significance |
| rs766660887 | 18:61,322,984 | A/T | — | uncertain significance |
| rs73962331 | 18:61,322,998 | G/A | — | benign |
| rs747263941 | 18:61,323,001 | A/T | — | uncertain significance |
| rs111442409 | 18:61,323,022 | C/T | — | uncertain significance |
| rs1181629101 | 18:61,323,049 | C/G | — | uncertain significance |
| rs1287831133 | 18:61,323,222 | T/A | — | uncertain significance |
| rs759286115 | 18:61,323,239 | C/A | — | uncertain significance |
| rs1241606881 | 18:61,323,255 | G/T | — | uncertain significance |
| rs1267678655 | 18:61,324,144 | T/A | — | uncertain significance |
| rs151099886 | 18:61,324,165 | G/A | — | likely benign |
| rs939413176 | 18:61,324,199 | T/A | — | uncertain significance |
| rs765803075 | 18:61,324,203 | T/C | — | uncertain significance |
| rs145445388 | 18:61,324,512 | G/A | — | uncertain significance |
| rs187183203 | 18:61,324,594 | C/G | — | uncertain significance |
| rs143773046 | 18:61,324,607 | C/T | — | likely benign |
| rs12457809 | 18:61,324,852 | G/A | intron variant | — |
| rs148254791 | 18:61,325,815 | A/G | — | likely benign |
| rs61754491 | 18:61,325,816 | C/T | — | likely benign |
| rs775420130 | 18:61,326,668 | T/C | — | uncertain significance |
| rs758787549 | 18:61,326,721 | A/G | — | uncertain significance |
| rs2511672922 | 18:61,328,368 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.