CNDP2
carnosine dipeptidase 2
Summary
CNDP2, also known as tissue carnosinase and peptidase A (EC 3.4.13.18), is a nonspecific dipeptidase rather than a selective carnosinase (Teufel et al., 2003 [PubMed 12473676]).[supplied by OMIM, Mar 2008]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6566810 | 18:72,163,459 | A/C | — | — |
| rs140583961 | 18:72,167,213 | C/T | — | uncertain significance |
| rs1978605892 | 18:72,167,241 | A/G | — | uncertain significance |
| rs778770816 | 18:72,168,585 | A/G | — | uncertain significance |
| rs199700693 | 18:72,168,594 | G/A | — | uncertain significance |
| rs200600524 | 18:72,168,601 | C/T | — | uncertain significance |
| rs151185140 | 18:72,168,607 | C/T | — | benign |
| rs751626393 | 18:72,173,106 | C/T | — | uncertain significance |
| rs1406456868 | 18:72,173,130 | G/T | — | uncertain significance |
| rs1367600763 | 18:72,173,159 | G/A | — | uncertain significance |
| rs1393458505 | 18:72,173,165 | A/G | — | uncertain significance |
| rs573310225 | 18:72,173,214 | A/G | — | uncertain significance |
| rs1428592608 | 18:72,173,222 | C/G | — | uncertain significance |
| rs561907242 | 18:72,173,255 | C/T | — | likely benign |
| rs34780792 | 18:72,173,278 | G/A | intron variant | — |
| rs12971120 | 18:72,174,023 | A/G | intron variant | — |
| rs375379348 | 18:72,176,114 | C/T | — | uncertain significance |
| rs773773845 | 18:72,176,121 | C/T | — | likely benign |
| rs747520460 | 18:72,176,122 | G/A | — | uncertain significance |
| rs764127312 | 18:72,176,137 | C/A | — | uncertain significance |
| rs143393947 | 18:72,176,159 | G/T | — | uncertain significance |
| rs2144596618 | 18:72,178,051 | A/T | — | uncertain significance |
| rs148388345 | 18:72,178,054 | C/T | — | uncertain significance |
| rs751859927 | 18:72,178,077 | C/T | — | likely benign |
| rs374633647 | 18:72,178,160 | A/G | — | uncertain significance |
| rs200391267 | 18:72,178,201 | C/G | — | uncertain significance |
| rs747958571 | 18:72,178,216 | G/A | — | uncertain significance |
| rs764151590 | 18:72,179,723 | G/C | — | uncertain significance |
| rs2512030659 | 18:72,179,725 | G/A | — | uncertain significance |
| rs144608297 | 18:72,180,812 | G/T | — | uncertain significance |
| rs752258037 | 18:72,180,832 | G/C | — | uncertain significance |
| rs1979486850 | 18:72,180,899 | A/G | — | uncertain significance |
| rs374013788 | 18:72,183,509 | A/G | — | uncertain significance |
| rs140933245 | 18:72,183,514 | A/G | — | uncertain significance |
| rs367547142 | 18:72,183,523 | G/A | — | uncertain significance |
| rs531994433 | 18:72,183,524 | C/G | — | uncertain significance |
| rs375477095 | 18:72,183,592 | G/A | — | uncertain significance |
| rs756324109 | 18:72,183,619 | G/A | — | likely benign |
| rs192178446 | 18:72,183,622 | G/A | — | uncertain significance |
| rs17089362 | 18:72,185,638 | G/A | — | — |
| rs149014910 | 18:72,185,770 | C/T | — | uncertain significance |
| rs147081657 | 18:72,185,771 | G/A | — | likely benign |
| rs1979850687 | 18:72,185,795 | A/G | — | uncertain significance |
| rs138489021 | 18:72,185,800 | G/A | — | uncertain significance |
| rs755632958 | 18:72,185,809 | G/A | — | uncertain significance |
| rs147167524 | 18:72,185,872 | A/G | — | uncertain significance |
| rs112548120 | 18:72,186,176 | C/A | — | benign |
| rs374297578 | 18:72,186,231 | G/A | — | uncertain significance |
| rs890336 | 18:72,187,612 | C/G | — | — |
| rs890335 | 18:72,188,252 | A/G | 3 prime UTR variant | — |
| rs890334 | 18:72,188,371 | A/T | — | — |
| rs12717111 | 18:72,189,250 | C/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.