ZNF787
zinc finger protein 787
Summary
Enables sequence-specific double-stranded 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 Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2514506789 | 19:56,599,403 | C/T | — | uncertain significance |
| rs4077285 | 19:56,599,405 | C/G | missense variant | — |
| rs202243737 | 19:56,599,455 | C/G | — | uncertain significance |
| rs1016781759 | 19:56,599,663 | G/A | — | uncertain significance |
| rs1985422066 | 19:56,599,714 | G/A | — | uncertain significance |
| rs2514508637 | 19:56,599,721 | C/G | — | uncertain significance |
| rs1332486890 | 19:56,599,742 | C/A | — | uncertain significance |
| rs1416227707 | 19:56,599,751 | C/T | — | uncertain significance |
| rs1985426570 | 19:56,599,757 | C/T | — | uncertain significance |
| rs1985427655 | 19:56,599,764 | C/T | — | uncertain significance |
| rs1985427983 | 19:56,599,766 | T/C | — | uncertain significance |
| rs2514508947 | 19:56,599,784 | C/A | — | uncertain significance |
| rs1167955551 | 19:56,599,798 | G/C | — | uncertain significance |
| rs1985433545 | 19:56,599,804 | A/C | — | uncertain significance |
| rs1169633554 | 19:56,599,832 | C/T | — | uncertain significance |
| rs2123385802 | 19:56,599,858 | G/A | — | uncertain significance |
| rs79066256 | 19:56,599,861 | A/G | — | likely benign |
| rs1985440358 | 19:56,599,908 | C/G | — | uncertain significance |
| rs765130005 | 19:56,599,978 | C/A | — | uncertain significance |
| rs530832675 | 19:56,600,090 | T/C | — | likely benign |
| rs1985454225 | 19:56,600,166 | C/G | — | uncertain significance |
| rs2514509885 | 19:56,600,167 | A/G | — | likely benign |
| rs775459906 | 19:56,600,251 | G/C | — | uncertain significance |
| rs762821507 | 19:56,600,252 | C/T | — | uncertain significance |
| rs1480313400 | 19:56,600,287 | T/C | — | uncertain significance |
| rs2514510280 | 19:56,600,351 | C/G | — | uncertain significance |
| rs767163771 | 19:56,600,389 | G/A | — | uncertain significance |
| rs200449995 | 19:56,600,442 | A/C | — | uncertain significance |
| rs150201146 | 19:56,614,214 | C/T | — | likely benign |
| rs56289422 | 19:56,615,173 | C/A | — | — |
| rs524829 | 19:56,623,139 | G/A | regulatory region variant | — |
| rs557602265 | 19:56,630,146 | G/A | — | — |
| rs473953 | 19:56,630,658 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.