ZNF440
zinc finger protein 440
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 Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs13382063 | 19:11,932,427 | A/G | regulatory region variant | — |
| rs368411263 | 19:11,941,161 | A/G | — | uncertain significance |
| rs375828267 | 19:11,941,183 | G/A | — | uncertain significance |
| rs424132 | 19:11,941,221 | T/A | — | benign |
| rs2512456069 | 19:11,942,196 | G/A | — | uncertain significance |
| rs376921276 | 19:11,942,228 | T/G | — | uncertain significance |
| rs780633623 | 19:11,942,361 | A/G | — | uncertain significance |
| rs1257126052 | 19:11,942,368 | G/A | — | uncertain significance |
| rs1179691732 | 19:11,942,482 | G/A | — | uncertain significance |
| rs771012865 | 19:11,942,505 | A/T | — | likely benign |
| rs375155828 | 19:11,942,527 | A/G | — | uncertain significance |
| rs758361355 | 19:11,942,590 | A/G | — | uncertain significance |
| rs1975945716 | 19:11,942,647 | A/G | — | uncertain significance |
| rs61746263 | 19:11,942,734 | G/T | — | uncertain significance |
| rs1249472634 | 19:11,942,737 | C/T | — | uncertain significance |
| rs765733465 | 19:11,942,746 | G/A | — | uncertain significance |
| rs993711527 | 19:11,942,789 | T/G | — | uncertain significance |
| rs201269465 | 19:11,942,805 | C/T | — | uncertain significance |
| rs183106198 | 19:11,942,872 | C/T | — | uncertain significance |
| rs892392283 | 19:11,942,874 | T/G | — | uncertain significance |
| rs368965098 | 19:11,942,880 | C/T | — | uncertain significance |
| rs140710381 | 19:11,942,935 | A/C | — | uncertain significance |
| rs766413832 | 19:11,942,982 | G/A | — | likely benign |
| rs1975953321 | 19:11,942,990 | G/C | — | uncertain significance |
| rs1338471654 | 19:11,943,024 | T/C | — | uncertain significance |
| rs562417997 | 19:11,943,182 | G/T | — | uncertain significance |
| rs368610345 | 19:11,943,190 | A/G | — | uncertain significance |
| rs200705543 | 19:11,943,225 | C/T | — | likely benign |
| rs374917320 | 19:11,943,226 | G/A | — | likely benign |
| rs2512458758 | 19:11,943,262 | A/G | — | uncertain significance |
| rs1484479402 | 19:11,943,264 | G/C | — | uncertain significance |
| rs200864155 | 19:11,943,360 | C/T | — | likely benign |
| rs755303446 | 19:11,943,361 | G/A | — | uncertain significance |
| rs374035788 | 19:11,943,364 | A/T | — | uncertain significance |
| rs753008670 | 19:11,943,465 | T/A | — | uncertain significance |
| rs2512459664 | 19:11,943,555 | A/G | — | uncertain significance |
| rs1039017774 | 19:11,943,586 | G/A | — | uncertain significance |
| rs191126694 | 19:11,943,636 | G/A | — | uncertain significance |
| rs755715970 | 19:11,943,675 | G/A | — | uncertain significance |
| rs866633329 | 19:11,943,690 | G/C | — | uncertain significance |
| rs143895808 | 19:11,943,693 | A/G | — | uncertain significance |
| rs1234223588 | 19:11,943,733 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.