ATF7IP
activating transcription factor 7 interacting protein
Summary
ATF7IP is a multifunctional nuclear protein that associates with heterochromatin. It can act as a transcriptional coactivator or corepressor depending upon its binding partners (summary by Liu et al., 2009 [PubMed 19106100]).[supplied by OMIM, Nov 2010]
Known Variants81 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10845988 | 12:14,521,182 | T/C | upstream gene variant | — |
| rs35309068 | 12:14,535,908 | T/G | intron variant | — |
| rs11055966 | 12:14,554,216 | G/A | intron variant | — |
| rs529846616 | 12:14,556,889 | A/G | — | — |
| rs4764086 | 12:14,568,452 | G/C | — | — |
| rs10772780 | 12:14,571,145 | T/A | — | — |
| rs1941685722 | 12:14,576,952 | G/A | — | uncertain significance |
| rs371570170 | 12:14,576,981 | A/C | — | uncertain significance |
| rs766682669 | 12:14,577,090 | C/T | — | likely benign |
| rs200012406 | 12:14,577,193 | A/G | — | uncertain significance |
| rs1427209991 | 12:14,577,205 | C/G | — | uncertain significance |
| rs146816712 | 12:14,577,234 | C/G | — | uncertain significance |
| rs200853057 | 12:14,577,265 | T/G | — | likely benign |
| rs140582861 | 12:14,577,288 | G/A | — | likely benign |
| rs145645055 | 12:14,577,294 | C/T | — | benign |
| rs747374218 | 12:14,577,313 | C/T | — | uncertain significance |
| rs751474951 | 12:14,577,412 | A/T | — | uncertain significance |
| rs2498811341 | 12:14,577,418 | C/T | — | uncertain significance |
| rs767326103 | 12:14,577,536 | A/G | — | uncertain significance |
| rs777048980 | 12:14,577,594 | C/A | — | uncertain significance |
| rs141145293 | 12:14,577,747 | G/C | — | uncertain significance |
| rs758639216 | 12:14,577,762 | A/G | — | uncertain significance |
| rs368557002 | 12:14,577,772 | C/G | — | uncertain significance |
| rs2498815668 | 12:14,577,797 | T/A | — | uncertain significance |
| rs114032760 | 12:14,577,851 | A/T | — | benign |
| rs770453777 | 12:14,577,876 | A/G | — | uncertain significance |
| rs1941758230 | 12:14,577,888 | G/T | — | uncertain significance |
| rs530346321 | 12:14,577,937 | G/A | — | uncertain significance |
| rs1376903808 | 12:14,577,985 | T/C | — | likely benign |
| rs762769025 | 12:14,578,018 | T/C | — | uncertain significance |
| rs372543706 | 12:14,578,042 | A/G | — | uncertain significance |
| rs1941770114 | 12:14,578,048 | A/T | — | uncertain significance |
| rs761938176 | 12:14,578,065 | C/A | — | uncertain significance |
| rs146351562 | 12:14,578,075 | C/T | — | uncertain significance |
| rs61754405 | 12:14,578,220 | C/T | — | likely benign |
| rs761585027 | 12:14,578,230 | G/A | — | uncertain significance |
| rs200627232 | 12:14,578,254 | G/C | — | uncertain significance |
| rs111490805 | 12:14,578,354 | C/T | — | likely benign |
| rs1941792630 | 12:14,578,377 | G/A | — | uncertain significance |
| rs374561365 | 12:14,578,384 | C/T | — | uncertain significance |
| rs755750746 | 12:14,578,392 | G/A | — | uncertain significance |
| rs145246872 | 12:14,587,298 | A/G | — | benign |
| rs3213764 | 12:14,587,301 | A/G | missense variant | benign |
| rs142252576 | 12:14,587,317 | G/C | — | uncertain significance |
| rs746767096 | 12:14,587,321 | G/A | — | uncertain significance |
| rs779331911 | 12:14,589,055 | G/A | — | uncertain significance |
| rs761806828 | 12:14,589,103 | G/A | — | uncertain significance |
| rs61758731 | 12:14,589,113 | G/C | — | likely benign |
| rs1942395586 | 12:14,589,129 | G/A | — | uncertain significance |
| rs754982380 | 12:14,589,169 | A/G | — | uncertain significance |
| rs7296122 | 12:14,594,740 | C/G | — | — |
| rs7964899 | 12:14,595,756 | G/A | intron variant | — |
| rs1379323026 | 12:14,599,980 | G/C | — | uncertain significance |
| rs74069866 | 12:14,613,471 | G/A | — | benign |
| rs770573335 | 12:14,613,566 | C/A | — | uncertain significance |
| rs1436654582 | 12:14,613,573 | C/T | — | uncertain significance |
| rs2498991797 | 12:14,613,617 | G/A | — | uncertain significance |
| rs71530944 | 12:14,613,631 | A/G | — | benign |
| rs74980854 | 12:14,613,779 | T/C | — | benign |
| rs767413966 | 12:14,613,815 | T/C | — | uncertain significance |
| rs2498992603 | 12:14,613,821 | C/A | — | uncertain significance |
| rs1438710889 | 12:14,613,830 | A/G | — | uncertain significance |
| rs775317636 | 12:14,613,832 | T/G | — | uncertain significance |
| rs149778571 | 12:14,613,840 | G/A | — | uncertain significance |
| rs145691516 | 12:14,613,848 | A/G | — | uncertain significance |
| rs377226980 | 12:14,613,849 | C/T | — | uncertain significance |
| rs2498992807 | 12:14,613,854 | A/G | — | uncertain significance |
| rs1453178261 | 12:14,613,963 | A/G | — | uncertain significance |
| rs1322444728 | 12:14,614,001 | A/G | — | uncertain significance |
| rs762398569 | 12:14,614,019 | A/G | — | uncertain significance |
| rs1002042475 | 12:14,614,031 | G/T | — | uncertain significance |
| rs745823360 | 12:14,619,496 | G/A | — | likely benign |
| rs55813566 | 12:14,622,317 | A/C | intron variant | — |
| rs10846002 | 12:14,626,421 | A/G | — | — |
| rs1591945738 | 12:14,628,831 | A/G | — | uncertain significance |
| rs71530945 | 12:14,634,044 | G/A | — | benign |
| rs7304399 | 12:14,645,350 | A/G | intron variant | — |
| rs2499193374 | 12:14,650,711 | A/C | — | uncertain significance |
| rs149615634 | 12:14,650,757 | G/A | — | uncertain significance |
| rs2499193594 | 12:14,650,766 | C/T | — | uncertain significance |
| rs2900333 | 12:14,653,867 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.