DELEC1
deleted in esophageal cancer 1
Summary
The function of this gene is not known. This gene is located in a region commonly deleted in esophageal squamous cell carcinomas. Gene expression is reduced or absent in these carcinomas and thus this is a candidate tumor suppressor gene for esophageal squamous cell carcinomas. [provided by RefSeq, Jul 2008]
Known Variants15 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7033388 | 9:117,909,509 | C/A | intron variant | — |
| rs4979507 | 9:117,929,972 | T/C | — | — |
| rs7470092 | 9:117,937,273 | A/G | regulatory region variant | — |
| rs55655124 | 9:117,939,494 | C/G | — | — |
| rs141683313 | 9:117,966,954 | C/A | intron variant | — |
| rs1014518150 | 9:118,002,829 | A/C | — | — |
| rs7026283 | 9:118,020,625 | G/C | upstream gene variant | — |
| rs7853844 | 9:118,050,414 | G/A | intron variant | — |
| rs144767096 | 9:118,106,763 | A/C | intron variant | — |
| rs10982711 | 9:118,121,694 | A/T | — | — |
| rs10817758 | 9:118,143,933 | C/T | intron variant | — |
| rs10982724 | 9:118,157,729 | T/G | — | — |
| rs2490487142 | 9:118,163,494 | G/C | — | uncertain significance |
| rs41307469 | 9:118,163,498 | A/G | — | benign |
| rs762473439 | 9:118,163,514 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.