CD248
CD248 molecule
Summary
Predicted to enable extracellular matrix binding activity and extracellular matrix protein binding activity. Predicted to be involved in cell migration. Predicted to act upstream of or within several processes, including fibroblast migration; lymph node development; and positive regulation of endothelial cell apoptotic process. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs182547559 | 11:66,082,215 | C/G | 3 prime UTR variant | — |
| rs2495284238 | 11:66,082,272 | G/A | — | uncertain significance |
| rs376112305 | 11:66,082,337 | C/T | — | uncertain significance |
| rs1345121341 | 11:66,082,351 | A/C | — | uncertain significance |
| rs754806986 | 11:66,082,358 | C/T | — | uncertain significance |
| rs747726735 | 11:66,082,365 | G/A | — | uncertain significance |
| rs2495284656 | 11:66,082,419 | G/T | — | uncertain significance |
| rs2495284707 | 11:66,082,457 | T/C | — | likely benign |
| rs145242086 | 11:66,082,468 | G/A | — | benign |
| rs1854527275 | 11:66,082,479 | C/G | — | uncertain significance |
| rs199624704 | 11:66,082,533 | C/T | — | uncertain significance |
| rs780843035 | 11:66,082,538 | T/G | — | uncertain significance |
| rs2495285207 | 11:66,082,659 | G/T | — | uncertain significance |
| rs7110351 | 11:66,082,705 | G/A | — | benign |
| rs150334610 | 11:66,082,740 | T/G | — | likely benign |
| rs772573119 | 11:66,082,749 | T/C | — | uncertain significance |
| rs2495285585 | 11:66,082,790 | G/A | — | uncertain significance |
| rs144952486 | 11:66,082,792 | G/C | — | benign |
| rs1163132338 | 11:66,082,794 | C/T | — | likely benign |
| rs969414987 | 11:66,082,862 | T/C | — | uncertain significance |
| rs140856103 | 11:66,082,890 | G/A | — | uncertain significance |
| rs145822705 | 11:66,082,904 | A/T | — | uncertain significance |
| rs138390105 | 11:66,082,914 | G/C | missense variant | — |
| rs1373059357 | 11:66,083,025 | G/C | — | uncertain significance |
| rs74818906 | 11:66,083,043 | C/T | — | benign |
| rs74494297 | 11:66,083,044 | G/A | — | benign |
| rs2495286264 | 11:66,083,107 | G/C | — | uncertain significance |
| rs750745496 | 11:66,083,138 | G/T | — | uncertain significance |
| rs377488212 | 11:66,083,148 | C/T | — | uncertain significance |
| rs766529516 | 11:66,083,151 | G/A | — | uncertain significance |
| rs115572668 | 11:66,083,158 | G/A | — | benign |
| rs78560344 | 11:66,083,263 | C/T | — | benign |
| rs148943512 | 11:66,083,269 | A/G | — | benign |
| rs146414594 | 11:66,083,330 | G/A | — | uncertain significance |
| rs114284078 | 11:66,083,362 | G/A | — | benign |
| rs1297193229 | 11:66,083,372 | T/G | — | uncertain significance |
| rs150281243 | 11:66,083,591 | G/A | — | likely benign |
| rs374192163 | 11:66,083,640 | C/T | — | uncertain significance |
| rs138260039 | 11:66,083,663 | G/A | — | uncertain significance |
| rs768605522 | 11:66,083,685 | C/T | — | uncertain significance |
| rs758800666 | 11:66,083,709 | G/C | — | uncertain significance |
| rs202021533 | 11:66,083,739 | C/T | — | uncertain significance |
| rs368665958 | 11:66,083,993 | T/A | — | uncertain significance |
| rs2495288794 | 11:66,084,027 | A/G | — | uncertain significance |
| rs759655028 | 11:66,084,078 | G/A | — | uncertain significance |
| rs757222983 | 11:66,084,096 | C/T | — | uncertain significance |
| rs2495289113 | 11:66,084,149 | C/A | — | uncertain significance |
| rs138322044 | 11:66,084,196 | G/A | — | benign |
| rs199828803 | 11:66,084,218 | C/T | — | uncertain significance |
| rs2495289380 | 11:66,084,230 | T/C | — | uncertain significance |
| rs115512520 | 11:66,084,244 | G/A | — | benign |
| rs541032235 | 11:66,084,258 | G/A | — | uncertain significance |
| rs751114440 | 11:66,084,293 | C/T | — | uncertain significance |
| rs749572714 | 11:66,084,340 | C/G | — | uncertain significance |
| rs769023822 | 11:66,084,342 | C/T | — | uncertain significance |
| rs199630152 | 11:66,084,374 | C/T | missense variant | — |
| rs750979307 | 11:66,084,381 | G/A | — | uncertain significance |
| rs750980250 | 11:66,084,405 | T/C | — | likely benign |
| rs1178531812 | 11:66,084,489 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.