ILDR1
immunoglobulin like domain containing receptor 1
Summary
This gene encodes a protein that contains an immunoglobulin-like domain. The encoded protein may function as a multimeric receptor at the cell surface. The expression of this gene may be a diagnostic marker for cancer progression. Alternatively spliced transcript variants encoding multiple protein isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]
Known Variants218 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs775202902 | 3:121,707,203 | G/A | — | uncertain significance |
| rs1576709293 | 3:121,707,218 | A/G | — | uncertain significance |
| rs568713946 | 3:121,707,242 | G/C | — | uncertain significance |
| rs752823578 | 3:121,707,265 | A/G | — | likely benign |
| rs567262350 | 3:121,707,268 | A/G | — | likely benign |
| rs11718322 | 3:121,710,086 | G/A | intron variant | — |
| rs12638492 | 3:121,711,763 | G/A | — | benign |
| rs80115089 | 3:121,711,766 | G/A | — | likely benign |
| rs751575285 | 3:121,711,998 | G/A | — | uncertain significance |
| rs201511787 | 3:121,712,002 | G/A | — | uncertain significance |
| rs727503095 | 3:121,712,014 | T/C | — | uncertain significance |
| rs142243054 | 3:121,712,015 | T/C | — | likely benign |
| rs369318229 | 3:121,712,036 | G/T | — | conflicting classifications of pathogenicity |
| rs2877561 | 3:121,712,051 | A/C | — | benign |
| rs767668911 | 3:121,712,059 | G/A | — | uncertain significance |
| rs149884253 | 3:121,712,069 | C/T | — | likely benign |
| rs374884043 | 3:121,712,070 | G/A | — | uncertain significance |
| rs200077106 | 3:121,712,080 | C/T | — | uncertain significance |
| rs146413045 | 3:121,712,088 | T/C | — | uncertain significance |
| rs745614639 | 3:121,712,089 | G/A | — | uncertain significance |
| rs778369601 | 3:121,712,092 | G/C | — | uncertain significance |
| rs34284625 | 3:121,712,098 | G/A | — | benign |
| rs144649620 | 3:121,712,099 | C/T | — | likely benign |
| rs367565247 | 3:121,712,105 | G/A | — | likely benign |
| rs757986659 | 3:121,712,109 | C/T | — | uncertain significance |
| rs777321422 | 3:121,712,110 | G/A | — | uncertain significance |
| rs149188951 | 3:121,712,118 | C/T | — | uncertain significance |
| rs556882881 | 3:121,712,119 | G/A | — | uncertain significance |
| rs189004426 | 3:121,712,135 | C/T | — | likely benign |
| rs2472800264 | 3:121,712,162 | G/C | — | likely benign |
| rs727503096 | 3:121,712,163 | G/A | — | uncertain significance |
| rs753090807 | 3:121,712,167 | T/G | — | uncertain significance |
| rs1183661317 | 3:121,712,171 | G/T | — | likely benign |
| rs372952499 | 3:121,712,174 | G/A | — | likely benign |
| rs745810698 | 3:121,712,197 | T/C | — | uncertain significance |
| rs199571441 | 3:121,712,208 | C/T | — | uncertain significance |
| rs200630651 | 3:121,712,211 | C/T | — | uncertain significance |
| rs775062249 | 3:121,712,212 | G/A | — | pathogenic |
| rs559855953 | 3:121,712,218 | C/T | — | likely benign |
| rs201105694 | 3:121,712,219 | G/A | — | conflicting classifications of pathogenicity |
| rs727503097 | 3:121,712,236 | C/T | — | uncertain significance |
| rs372564314 | 3:121,712,238 | C/T | — | conflicting classifications of pathogenicity |
| rs376986803 | 3:121,712,239 | G/A | — | uncertain significance |
| rs180838731 | 3:121,712,254 | G/A | — | uncertain significance |
| rs148350512 | 3:121,712,270 | G/T | — | likely benign |
| rs34883204 | 3:121,712,271 | C/T | — | benign |
| rs141559449 | 3:121,712,272 | G/A | — | conflicting classifications of pathogenicity |
| rs763407271 | 3:121,712,273 | G/A | — | likely benign |
| rs554966703 | 3:121,712,284 | G/A | — | uncertain significance |
| rs2472801055 | 3:121,712,290 | G/A | — | uncertain significance |
| rs35597690 | 3:121,712,291 | G/T | — | likely benign |
| rs760257421 | 3:121,712,295 | G/A | — | uncertain significance |
| rs35906279 | 3:121,712,298 | C/T | — | benign |
| rs140567004 | 3:121,712,299 | G/A | — | uncertain significance |
| rs794727852 | 3:121,712,304 | C/T | — | uncertain significance |
| rs376510686 | 3:121,712,305 | G/A | — | uncertain significance |
| rs1172585670 | 3:121,712,329 | C/T | — | uncertain significance |
| rs2472801327 | 3:121,712,343 | C/T | — | uncertain significance |
| rs140777020 | 3:121,712,351 | C/A | — | uncertain significance |
| rs756244874 | 3:121,712,356 | G/A | — | uncertain significance |
| rs16832645 | 3:121,712,358 | A/G | — | benign |
| rs144533401 | 3:121,712,361 | G/A | — | uncertain significance |
| rs148486121 | 3:121,712,369 | A/G | — | likely benign |
| rs150479416 | 3:121,712,385 | C/T | — | uncertain significance |
| rs759613864 | 3:121,712,386 | G/T | — | uncertain significance |
| rs139810461 | 3:121,712,402 | C/T | — | likely benign |
| rs369610198 | 3:121,712,403 | G/A | — | uncertain significance |
| rs1288021402 | 3:121,712,410 | C/T | — | uncertain significance |
| rs143311654 | 3:121,712,412 | A/G | — | uncertain significance |
| rs373563420 | 3:121,712,420 | T/G | — | uncertain significance |
| rs543019223 | 3:121,712,427 | A/G | — | uncertain significance |
| rs1576715040 | 3:121,712,428 | A/G | — | likely benign |
| rs146697721 | 3:121,712,431 | C/T | — | uncertain significance |
| rs35661993 | 3:121,712,434 | A/G | — | benign |
| rs746732835 | 3:121,712,436 | G/C | — | conflicting classifications of pathogenicity |
| rs150250182 | 3:121,712,437 | A/G | — | conflicting classifications of pathogenicity |
| rs1553743331 | 3:121,712,438 | C/G | — | uncertain significance |
| rs776320185 | 3:121,712,448 | C/T | — | uncertain significance |
| rs1553743343 | 3:121,712,459 | C/G | — | uncertain significance |
| rs387907015 | 3:121,712,461 | C/A | stop gained | pathogenic |
| rs763959563 | 3:121,712,476 | G/A | — | uncertain significance |
| rs751310993 | 3:121,712,509 | C/T | — | uncertain significance |
| rs147113814 | 3:121,712,540 | C/G | — | uncertain significance |
| rs1297610101 | 3:121,712,565 | C/T | — | uncertain significance |
| rs370057056 | 3:121,712,598 | G/A | — | uncertain significance |
| rs778078949 | 3:121,712,617 | G/A | — | uncertain significance |
| rs372613583 | 3:121,712,623 | C/T | — | uncertain significance |
| rs138334785 | 3:121,712,624 | G/A | — | likely benign |
| rs1428349007 | 3:121,712,629 | C/T | — | uncertain significance |
| rs1553743398 | 3:121,712,646 | A/C | — | uncertain significance |
| rs759699080 | 3:121,712,650 | T/A | — | uncertain significance |
| rs752714222 | 3:121,712,654 | G/T | — | pathogenic |
| rs199882599 | 3:121,712,667 | A/C | — | uncertain significance |
| rs370886914 | 3:121,712,675 | T/C | — | likely benign |
| rs779657821 | 3:121,712,680 | G/A | — | uncertain significance |
| rs771867997 | 3:121,712,711 | G/T | — | uncertain significance |
| rs2107644765 | 3:121,712,713 | T/C | — | uncertain significance |
| rs146278176 | 3:121,712,715 | C/T | — | uncertain significance |
| rs139164443 | 3:121,712,716 | G/A | — | uncertain significance |
| rs141450561 | 3:121,712,730 | A/C | — | conflicting classifications of pathogenicity |
Showing 100 of 218 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.