ZNF77
zinc finger protein 77
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2088362944 | 19:2,933,588 | T/G | — | uncertain significance |
| rs372798240 | 19:2,933,594 | C/T | — | uncertain significance |
| rs112261253 | 19:2,933,611 | G/A | — | uncertain significance |
| rs34789013 | 19:2,933,649 | G/C | — | benign |
| rs770250071 | 19:2,933,678 | C/G | — | uncertain significance |
| rs139829692 | 19:2,933,698 | G/T | — | uncertain significance |
| rs761501139 | 19:2,933,699 | C/T | — | uncertain significance |
| rs2512059968 | 19:2,933,730 | T/A | — | uncertain significance |
| rs142625963 | 19:2,933,737 | G/A | — | uncertain significance |
| rs1381072665 | 19:2,933,804 | A/C | — | uncertain significance |
| rs1242397158 | 19:2,933,819 | A/G | — | uncertain significance |
| rs374051858 | 19:2,933,839 | G/A | — | uncertain significance |
| rs767198873 | 19:2,933,957 | C/T | — | uncertain significance |
| rs374049271 | 19:2,934,022 | C/T | — | uncertain significance |
| rs370214322 | 19:2,934,056 | A/G | — | uncertain significance |
| rs1205337661 | 19:2,934,059 | C/T | — | uncertain significance |
| rs2088371352 | 19:2,934,086 | T/C | — | uncertain significance |
| rs759981598 | 19:2,934,100 | T/C | — | uncertain significance |
| rs146879198 | 19:2,934,107 | G/A | stop gained | — |
| rs2088371883 | 19:2,934,124 | G/C | — | uncertain significance |
| rs369325243 | 19:2,934,149 | A/T | — | uncertain significance |
| rs542089630 | 19:2,934,150 | C/A | — | uncertain significance |
| rs767236655 | 19:2,934,218 | T/C | — | uncertain significance |
| rs141673139 | 19:2,934,241 | G/A | — | uncertain significance |
| rs145980708 | 19:2,934,260 | T/C | — | uncertain significance |
| rs780516253 | 19:2,934,263 | T/C | — | uncertain significance |
| rs1223515632 | 19:2,934,291 | G/C | — | uncertain significance |
| rs2088374626 | 19:2,934,292 | C/G | — | uncertain significance |
| rs1192298280 | 19:2,934,325 | G/A | — | uncertain significance |
| rs141544349 | 19:2,934,345 | T/G | — | uncertain significance |
| rs2144958384 | 19:2,934,401 | A/G | — | uncertain significance |
| rs762044224 | 19:2,934,437 | G/A | — | uncertain significance |
| rs35994793 | 19:2,934,480 | C/G | — | uncertain significance |
| rs767962381 | 19:2,934,535 | G/C | — | likely benign |
| rs2512062085 | 19:2,934,562 | T/G | — | uncertain significance |
| rs1392901794 | 19:2,934,586 | G/A | — | uncertain significance |
| rs2512062171 | 19:2,934,601 | G/A | — | uncertain significance |
| rs34727043 | 19:2,934,602 | A/C | — | benign |
| rs1599617104 | 19:2,934,713 | C/T | — | uncertain significance |
| rs1353464813 | 19:2,934,733 | A/G | — | uncertain significance |
| rs373024650 | 19:2,934,745 | G/A | — | uncertain significance |
| rs113047444 | 19:2,934,809 | G/T | — | uncertain significance |
| rs35699176 | 19:2,936,535 | G/A | stop gained | — |
| rs200864167 | 19:2,936,559 | T/C | — | uncertain significance |
| rs35020820 | 19:2,936,575 | A/G | — | benign |
| rs747168418 | 19:2,936,622 | T/C | — | uncertain significance |
| rs201889891 | 19:2,936,648 | C/G | — | uncertain significance |
| rs139544741 | 19:2,936,660 | C/T | — | uncertain significance |
| rs756279372 | 19:2,936,694 | T/G | — | uncertain significance |
| rs748678409 | 19:2,936,698 | A/C | — | uncertain significance |
| rs12608916 | 19:2,939,289 | A/C | — | likely benign |
| rs1404880574 | 19:2,939,399 | C/A | — | uncertain significance |
| rs966673235 | 19:2,939,405 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.