TNFRSF10A
TNF receptor superfamily member 10a
Summary
The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is activated by tumor necrosis factor-related apoptosis inducing ligand (TNFSF10/TRAIL), and thus transduces cell death signal and induces cell apoptosis. Studies with FADD-deficient mice suggested that FADD, a death domain containing adaptor protein, is required for the apoptosis mediated by this protein. [provided by RefSeq, Jul 2008]
Known Variants69 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs184818272 | 8:23,048,612 | C/T | downstream gene variant | — |
| rs144773234 | 8:23,049,208 | C/A | — | benign |
| rs77368365 | 8:23,049,273 | G/C | — | benign |
| rs2230229 | 8:23,049,292 | C/T | missense variant | — |
| rs1283179595 | 8:23,049,301 | C/T | — | uncertain significance |
| rs1385591726 | 8:23,049,313 | C/G | — | uncertain significance |
| rs769671166 | 8:23,049,352 | C/T | — | uncertain significance |
| rs1169854819 | 8:23,049,401 | C/T | — | uncertain significance |
| rs754627550 | 8:23,049,417 | A/G | — | likely benign |
| rs780590308 | 8:23,049,418 | G/C | — | uncertain significance |
| rs747598220 | 8:23,049,419 | C/T | — | uncertain significance |
| rs1297649662 | 8:23,049,471 | G/T | — | uncertain significance |
| rs373540814 | 8:23,049,479 | A/G | — | uncertain significance |
| rs777239727 | 8:23,049,491 | C/T | — | uncertain significance |
| rs78885531 | 8:23,054,635 | A/C | — | benign |
| rs75047372 | 8:23,054,638 | C/T | — | benign |
| rs140442292 | 8:23,054,646 | C/G | — | uncertain significance |
| rs145301693 | 8:23,054,662 | C/T | — | uncertain significance |
| rs138069770 | 8:23,054,713 | G/A | — | uncertain significance |
| rs148383409 | 8:23,056,860 | A/G | — | benign |
| rs571095882 | 8:23,056,865 | C/A | — | uncertain significance |
| rs2230230 | 8:23,056,887 | G/A | — | benign |
| rs149391935 | 8:23,056,902 | G/A | — | benign |
| rs17088980 | 8:23,056,904 | T/G | — | benign |
| rs1800873765 | 8:23,056,930 | C/A | — | uncertain significance |
| rs748925595 | 8:23,056,940 | G/C | — | uncertain significance |
| rs144670447 | 8:23,056,948 | C/T | — | uncertain significance |
| rs2235126 | 8:23,057,181 | C/T | intron variant | — |
| rs762045833 | 8:23,057,417 | G/C | — | uncertain significance |
| rs375941892 | 8:23,058,100 | A/G | — | likely benign |
| rs4872077 | 8:23,058,188 | C/T | — | benign |
| rs20576 | 8:23,058,220 | T/G | missense variant | benign |
| rs368869003 | 8:23,058,251 | C/A | — | uncertain significance |
| rs756047313 | 8:23,058,253 | T/G | — | uncertain significance |
| rs144093718 | 8:23,058,270 | G/C | — | uncertain significance |
| rs146469828 | 8:23,059,322 | C/T | — | uncertain significance |
| rs20575 | 8:23,059,324 | C/A | missense variant | — |
| rs150096329 | 8:23,059,363 | C/T | — | uncertain significance |
| rs1480108021 | 8:23,059,388 | A/T | — | uncertain significance |
| rs974859695 | 8:23,059,414 | G/A | — | uncertain significance |
| rs182707081 | 8:23,060,155 | C/G | — | likely benign |
| rs370841687 | 8:23,060,203 | T/C | — | uncertain significance |
| rs149012704 | 8:23,060,213 | G/T | — | likely benign |
| rs755780790 | 8:23,060,222 | C/T | — | likely benign |
| rs17620 | 8:23,060,256 | T/C | missense variant | — |
| rs776832652 | 8:23,060,258 | T/G | — | uncertain significance |
| rs4242392 | 8:23,061,633 | T/C | upstream gene variant | — |
| rs540165698 | 8:23,064,957 | T/C | — | — |
| rs13255997 | 8:23,068,286 | A/G | downstream gene variant | — |
| rs200630980 | 8:23,069,635 | G/A | — | uncertain significance |
| rs483352726 | 8:23,069,677 | C/T | — | uncertain significance |
| rs540722209 | 8:23,079,147 | C/T | — | — |
| rs1000294 | 8:23,080,135 | G/T | — | — |
| rs34601117 | 8:23,082,264 | C/G | — | benign |
| rs904680412 | 8:23,082,270 | T/G | — | uncertain significance |
| rs765900944 | 8:23,082,280 | C/A | — | uncertain significance |
| rs752552572 | 8:23,082,294 | A/G | — | uncertain significance |
| rs772267982 | 8:23,082,339 | G/A | — | uncertain significance |
| rs61756236 | 8:23,082,369 | C/G | — | benign |
| rs1801316873 | 8:23,082,387 | C/T | — | uncertain significance |
| rs777061458 | 8:23,082,433 | G/C | — | uncertain significance |
| rs549217117 | 8:23,082,465 | A/C | — | uncertain significance |
| rs943381828 | 8:23,082,466 | C/T | — | uncertain significance |
| rs2486399871 | 8:23,082,483 | G/T | — | uncertain significance |
| rs758645078 | 8:23,082,490 | C/T | — | uncertain significance |
| rs775203714 | 8:23,082,518 | A/T | — | uncertain significance |
| rs368319860 | 8:23,082,554 | T/A | — | uncertain significance |
| rs13278062 | 8:23,082,971 | G/T | coding sequence variant | not provided |
| rs73224404 | 8:23,083,501 | A/G | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.