CPN2
carboxypeptidase N subunit 2
Summary
Predicted to enable enzyme regulator activity. Predicted to be involved in protein stabilization. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs542465761 | 3:194,060,959 | G/A | — | — |
| rs1048996 | 3:194,061,043 | G/C | — | — |
| rs141044584 | 3:194,061,835 | G/A | — | uncertain significance |
| rs141360992 | 3:194,061,934 | G/A | — | uncertain significance |
| rs111646477 | 3:194,061,955 | C/T | — | uncertain significance |
| rs574415043 | 3:194,061,984 | T/C | — | uncertain significance |
| rs1712802244 | 3:194,061,988 | T/C | — | uncertain significance |
| rs138428290 | 3:194,061,995 | G/C | — | uncertain significance |
| rs1341520913 | 3:194,061,996 | C/T | — | uncertain significance |
| rs1712807908 | 3:194,062,060 | A/G | — | uncertain significance |
| rs142681810 | 3:194,062,087 | G/A | — | uncertain significance |
| rs1446759375 | 3:194,062,135 | G/C | — | uncertain significance |
| rs759367695 | 3:194,062,186 | G/A | — | uncertain significance |
| rs772116328 | 3:194,062,189 | C/T | — | uncertain significance |
| rs745318743 | 3:194,062,288 | C/T | — | uncertain significance |
| rs2108646063 | 3:194,062,323 | T/C | — | likely benign |
| rs1457849058 | 3:194,062,327 | A/G | — | uncertain significance |
| rs779582769 | 3:194,062,387 | G/A | — | uncertain significance |
| rs148901764 | 3:194,062,423 | C/T | — | uncertain significance |
| rs1380930772 | 3:194,062,482 | G/T | — | uncertain significance |
| rs1254390481 | 3:194,062,498 | G/C | — | uncertain significance |
| rs1257416060 | 3:194,062,501 | G/A | — | uncertain significance |
| rs149427019 | 3:194,062,677 | G/A | — | benign |
| rs144821969 | 3:194,062,684 | G/A | — | uncertain significance |
| rs199990965 | 3:194,062,731 | G/A | — | uncertain significance |
| rs1359473481 | 3:194,062,743 | G/A | — | uncertain significance |
| rs753796030 | 3:194,062,765 | A/G | — | uncertain significance |
| rs375218643 | 3:194,062,807 | G/A | — | uncertain significance |
| rs143748840 | 3:194,062,878 | G/A | — | uncertain significance |
| rs772293956 | 3:194,062,894 | G/C | — | uncertain significance |
| rs146780118 | 3:194,062,924 | G/A | — | uncertain significance |
| rs1712869610 | 3:194,062,941 | A/G | — | uncertain significance |
| rs2473937226 | 3:194,062,984 | G/T | — | uncertain significance |
| rs199846219 | 3:194,063,002 | G/C | — | uncertain significance |
| rs140462752 | 3:194,063,005 | G/T | — | uncertain significance |
| rs1466248478 | 3:194,063,032 | C/T | — | uncertain significance |
| rs1279135373 | 3:194,063,036 | C/T | — | uncertain significance |
| rs201648991 | 3:194,063,040 | T/A | — | uncertain significance |
| rs1401989199 | 3:194,063,125 | C/T | — | uncertain significance |
| rs1438277511 | 3:194,063,152 | C/T | — | uncertain significance |
| rs763043511 | 3:194,063,216 | G/T | — | uncertain significance |
| rs143058335 | 3:194,063,253 | G/A | — | uncertain significance |
| rs772064450 | 3:194,063,284 | A/G | — | likely benign |
| rs1576989311 | 3:194,063,334 | A/G | — | uncertain significance |
| rs1712900353 | 3:194,063,376 | G/A | — | uncertain significance |
| rs140187491 | 3:194,063,390 | G/C | — | benign |
| rs7630163 | 3:194,064,298 | C/A | intron variant | — |
| rs529517393 | 3:194,074,018 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.