TOX
thymocyte selection associated high mobility group box
Summary
The protein encoded by this gene contains a HMG box DNA binding domain. HMG boxes are found in many eukaryotic proteins involved in chromatin assembly, transcription and replication. This protein may function to regulate T-cell development.[provided by RefSeq, Apr 2009]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2536652999 | 8:59,720,334 | T/C | — | uncertain significance |
| rs201487566 | 8:59,720,716 | G/T | — | uncertain significance |
| rs755315892 | 8:59,720,719 | G/A | — | uncertain significance |
| rs2536653545 | 8:59,720,761 | G/C | — | uncertain significance |
| rs1381503098 | 8:59,728,000 | T/A | — | uncertain significance |
| rs772328073 | 8:59,728,005 | G/T | — | uncertain significance |
| rs762533510 | 8:59,728,082 | G/T | — | uncertain significance |
| rs138337223 | 8:59,728,090 | G/A | — | uncertain significance |
| rs1411747146 | 8:59,728,123 | T/C | — | uncertain significance |
| rs1297783743 | 8:59,728,147 | A/G | — | uncertain significance |
| rs143343596 | 8:59,728,153 | G/A | — | uncertain significance |
| rs201823077 | 8:59,728,189 | G/A | — | uncertain significance |
| rs374396949 | 8:59,728,262 | C/T | — | uncertain significance |
| rs534762644 | 8:59,760,071 | T/C | — | — |
| rs1075418 | 8:59,763,910 | T/C | regulatory region variant | — |
| rs531597509 | 8:59,764,098 | G/A | — | likely benign |
| rs761024434 | 8:59,764,249 | T/C | — | uncertain significance |
| rs753391814 | 8:59,764,254 | C/T | — | uncertain significance |
| rs13268621 | 8:59,811,724 | T/G | intron variant | — |
| rs2326213 | 8:59,812,459 | A/G | intron variant | — |
| rs4738734 | 8:59,814,330 | A/T | intron variant | — |
| rs13261666 | 8:59,814,666 | G/A | — | — |
| rs13263261 | 8:59,814,688 | T/C | — | — |
| rs9298002 | 8:59,815,118 | T/C | intron variant | — |
| rs568943075 | 8:59,842,148 | T/C | — | — |
| rs1236627019 | 8:59,851,961 | C/T | — | uncertain significance |
| rs143452038 | 8:59,852,001 | A/G | — | likely benign |
| rs1443441902 | 8:59,852,042 | G/A | — | uncertain significance |
| rs564719882 | 8:59,872,518 | T/C | — | uncertain significance |
| rs2486942028 | 8:59,872,545 | A/G | — | uncertain significance |
| rs11777927 | 8:59,881,039 | A/C | — | — |
| rs139280526 | 8:60,031,474 | G/C | — | uncertain significance |
| rs376055079 | 8:60,031,540 | C/T | — | uncertain significance |
| rs780921856 | 8:60,031,542 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.