CDCP2
CUB domain containing protein 2
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs41294792 | 1:54,605,242 | G/A | — | uncertain significance |
| rs747338763 | 1:54,605,246 | C/T | — | likely benign |
| rs146464941 | 1:54,605,251 | A/G | — | likely benign |
| rs369800097 | 1:54,605,258 | G/C | — | uncertain significance |
| rs75306471 | 1:54,605,320 | G/A | — | uncertain significance |
| rs146671242 | 1:54,605,429 | C/T | — | uncertain significance |
| rs757653123 | 1:54,605,449 | C/T | — | uncertain significance |
| rs1659328171 | 1:54,605,458 | G/A | — | uncertain significance |
| rs541638967 | 1:54,605,467 | C/T | — | uncertain significance |
| rs138864964 | 1:54,605,557 | G/T | missense variant | — |
| rs557044023 | 1:54,605,564 | C/T | — | uncertain significance |
| rs780044296 | 1:54,605,572 | C/T | — | uncertain significance |
| rs2524990232 | 1:54,605,653 | A/C | — | uncertain significance |
| rs775186450 | 1:54,606,797 | C/G | — | uncertain significance |
| rs753051915 | 1:54,606,840 | C/T | — | uncertain significance |
| rs569599539 | 1:54,606,855 | C/T | — | uncertain significance |
| rs202201685 | 1:54,606,867 | G/C | — | uncertain significance |
| rs2524995282 | 1:54,606,923 | G/A | — | uncertain significance |
| rs1224697505 | 1:54,606,962 | T/A | — | uncertain significance |
| rs2524995568 | 1:54,606,977 | A/T | — | uncertain significance |
| rs150513591 | 1:54,606,996 | G/A | — | uncertain significance |
| rs1353661711 | 1:54,606,999 | C/G | — | uncertain significance |
| rs747760888 | 1:54,607,008 | G/A | — | uncertain significance |
| rs2524995817 | 1:54,607,019 | T/A | — | uncertain significance |
| rs374398380 | 1:54,607,037 | G/A | — | uncertain significance |
| rs775362180 | 1:54,607,044 | T/A | — | uncertain significance |
| rs750875550 | 1:54,607,073 | C/A | — | uncertain significance |
| rs372468657 | 1:54,607,092 | C/T | — | uncertain significance |
| rs144870678 | 1:54,610,150 | C/T | — | conflicting classifications of pathogenicity |
| rs2525005677 | 1:54,610,162 | C/G | — | uncertain significance |
| rs756054521 | 1:54,610,203 | C/T | — | uncertain significance |
| rs183163862 | 1:54,610,234 | G/A | — | uncertain significance |
| rs200942058 | 1:54,610,305 | A/C | — | uncertain significance |
| rs1659430628 | 1:54,610,312 | A/C | — | uncertain significance |
| rs368164700 | 1:54,610,323 | G/T | — | uncertain significance |
| rs777313754 | 1:54,610,445 | A/C | — | uncertain significance |
| rs779659965 | 1:54,618,577 | C/T | — | uncertain significance |
| rs749165222 | 1:54,618,579 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.