CEACAM20
CEA cell adhesion molecule 20
Summary
Predicted to enable protein tyrosine kinase binding activity. Predicted to be involved in regulation of immune system process and signal transduction. Predicted to be located in apical plasma membrane and microvillus membrane. Predicted to be active in cell surface and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs753102567 | 19:45,015,107 | T/A | — | uncertain significance |
| rs951414714 | 19:45,015,158 | G/A | — | uncertain significance |
| rs2513625430 | 19:45,015,720 | G/A | — | uncertain significance |
| rs111978729 | 19:45,015,911 | G/A | — | — |
| rs1971018925 | 19:45,016,124 | G/A | — | uncertain significance |
| rs759138689 | 19:45,017,239 | A/C | — | uncertain significance |
| rs1235376 | 19:45,017,496 | G/T | — | — |
| rs546432549 | 19:45,019,170 | A/C | — | — |
| rs185633112 | 19:45,020,490 | G/T | intron variant | — |
| rs771251987 | 19:45,021,036 | C/T | — | uncertain significance |
| rs200628672 | 19:45,021,039 | G/A | coding sequence variant | Uncertain significance |
| rs767634070 | 19:45,021,082 | C/T | — | uncertain significance |
| rs760111245 | 19:45,021,159 | C/T | — | likely benign |
| rs776098638 | 19:45,021,256 | C/G | — | uncertain significance |
| rs190377922 | 19:45,023,645 | C/A | intron variant | — |
| rs200961907 | 19:45,024,535 | T/C | — | uncertain significance |
| rs533196199 | 19:45,024,538 | G/A | — | uncertain significance |
| rs769872105 | 19:45,024,543 | C/T | — | likely benign |
| rs766902386 | 19:45,024,591 | C/T | — | uncertain significance |
| rs2513656564 | 19:45,024,616 | T/A | — | uncertain significance |
| rs371139859 | 19:45,024,681 | T/C | — | uncertain significance |
| rs1472751572 | 19:45,024,684 | A/G | — | uncertain significance |
| rs367917751 | 19:45,024,775 | T/C | — | uncertain significance |
| rs773887584 | 19:45,026,675 | C/A | — | uncertain significance |
| rs2513664060 | 19:45,026,764 | A/T | — | uncertain significance |
| rs1351442258 | 19:45,026,857 | G/T | — | uncertain significance |
| rs753715606 | 19:45,026,869 | C/A | — | uncertain significance |
| rs756950141 | 19:45,026,872 | T/C | — | uncertain significance |
| rs372020630 | 19:45,028,043 | C/T | — | uncertain significance |
| rs562062188 | 19:45,028,044 | G/C | — | uncertain significance |
| rs887325240 | 19:45,028,064 | C/T | — | uncertain significance |
| rs2513669520 | 19:45,028,096 | T/C | — | uncertain significance |
| rs35443082 | 19:45,028,112 | T/C | coding sequence variant | — |
| rs779566628 | 19:45,028,154 | G/A | — | uncertain significance |
| rs373440198 | 19:45,029,142 | C/T | — | uncertain significance |
| rs991002599 | 19:45,029,166 | G/A | — | uncertain significance |
| rs372782771 | 19:45,029,199 | C/T | — | uncertain significance |
| rs370505366 | 19:45,029,218 | G/C | — | uncertain significance |
| rs371366149 | 19:45,029,263 | C/T | — | uncertain significance |
| rs62116894 | 19:45,031,301 | G/C | — | — |
| rs753981648 | 19:45,033,495 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.