CPQ
carboxypeptidase Q
Summary
This gene encodes a metallopeptidase that belongs to the peptidase M28 family. The encoded protein may catalyze the cleavage of dipeptides with unsubstituted terminals into amino acids. [provided by RefSeq, Jul 2013]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs192039518 | 8:97,672,767 | C/A | intron variant | — |
| rs149364428 | 8:97,737,741 | G/A | intron variant | — |
| rs59093198 | 8:97,740,267 | C/T | intron variant | — |
| rs3763558 | 8:97,796,731 | C/A | intron variant | — |
| rs183172032 | 8:97,797,144 | G/T | — | uncertain significance |
| rs2487894091 | 8:97,797,233 | A/G | — | uncertain significance |
| rs2487894138 | 8:97,797,260 | T/A | — | uncertain significance |
| rs145622173 | 8:97,797,273 | A/G | — | uncertain significance |
| rs2487894236 | 8:97,797,310 | G/A | — | uncertain significance |
| rs149981793 | 8:97,797,399 | T/G | — | benign |
| rs748190900 | 8:97,797,433 | T/A | — | uncertain significance |
| rs372650907 | 8:97,797,471 | G/C | — | uncertain significance |
| rs772572771 | 8:97,797,507 | C/T | — | uncertain significance |
| rs1563496636 | 8:97,797,516 | G/A | — | uncertain significance |
| rs34088584 | 8:97,797,538 | G/A | — | benign |
| rs751928165 | 8:97,797,541 | T/C | — | uncertain significance |
| rs201126730 | 8:97,797,566 | T/C | — | benign |
| rs148279743 | 8:97,847,219 | T/C | — | benign |
| rs145853886 | 8:97,847,228 | C/T | — | uncertain significance |
| rs1324778651 | 8:97,847,300 | T/A | — | uncertain significance |
| rs774866806 | 8:97,847,312 | G/A | — | uncertain significance |
| rs571560641 | 8:97,847,339 | C/T | — | uncertain significance |
| rs113247437 | 8:97,847,377 | A/G | — | benign |
| rs201297204 | 8:97,847,386 | G/A | — | uncertain significance |
| rs180816202 | 8:97,867,920 | C/A | intron variant | — |
| rs368218633 | 8:97,892,082 | G/A | — | uncertain significance |
| rs141107654 | 8:97,892,119 | G/A | missense variant | — |
| rs11984922 | 8:98,024,009 | T/C | intron variant | — |
| rs753340797 | 8:98,041,636 | C/T | — | uncertain significance |
| rs79424797 | 8:98,041,654 | C/A | — | benign |
| rs7840421 | 8:98,041,659 | G/A | — | benign |
| rs147742864 | 8:98,049,907 | T/C | intron variant | — |
| rs77641092 | 8:98,067,782 | G/A | intron variant | — |
| rs535633989 | 8:98,078,283 | C/A | — | uncertain significance |
| rs769332836 | 8:98,078,346 | T/C | — | uncertain significance |
| rs933794332 | 8:98,078,369 | A/G | — | uncertain significance |
| rs150689132 | 8:98,078,379 | A/G | — | uncertain significance |
| rs765251664 | 8:98,078,414 | T/A | — | uncertain significance |
| rs750399271 | 8:98,078,418 | G/C | — | uncertain significance |
| rs17737465 | 8:98,154,441 | A/G | upstream gene variant | — |
| rs200394841 | 8:98,155,286 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.