ZNF577
zinc finger protein 577
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-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 Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs62110082 | 19:52,338,641 | T/A | — | — |
| rs4802878 | 19:52,340,313 | G/C | — | — |
| rs721890 | 19:52,341,061 | T/C | — | — |
| rs721889 | 19:52,341,249 | A/T | — | — |
| rs1468642 | 19:52,341,757 | T/A | downstream gene variant | — |
| rs10411161 | 19:52,372,976 | C/A | — | — |
| rs139796205 | 19:52,375,851 | A/C | — | uncertain significance |
| rs763951497 | 19:52,375,861 | C/T | — | uncertain significance |
| rs376895478 | 19:52,375,975 | G/A | — | uncertain significance |
| rs764971465 | 19:52,375,999 | A/G | — | uncertain significance |
| rs146682852 | 19:52,376,032 | A/T | — | uncertain significance |
| rs2514065893 | 19:52,376,276 | C/T | — | uncertain significance |
| rs752033229 | 19:52,376,343 | G/C | — | uncertain significance |
| rs767787433 | 19:52,376,365 | G/A | — | uncertain significance |
| rs559256688 | 19:52,376,384 | C/A | — | uncertain significance |
| rs1468254499 | 19:52,376,442 | C/A | — | uncertain significance |
| rs142925012 | 19:52,376,458 | C/T | — | uncertain significance |
| rs372428716 | 19:52,376,470 | T/C | — | likely benign |
| rs142666241 | 19:52,376,476 | C/T | — | uncertain significance |
| rs768421805 | 19:52,376,485 | C/T | — | uncertain significance |
| rs2084694632 | 19:52,376,513 | A/T | — | uncertain significance |
| rs578213047 | 19:52,376,533 | G/A | — | uncertain significance |
| rs1376787477 | 19:52,376,607 | C/G | — | uncertain significance |
| rs199990461 | 19:52,376,683 | C/A | — | uncertain significance |
| rs766279073 | 19:52,376,689 | G/A | — | uncertain significance |
| rs560523486 | 19:52,376,719 | T/C | — | likely benign |
| rs200063901 | 19:52,376,753 | C/T | — | uncertain significance |
| rs528181607 | 19:52,376,759 | C/T | — | uncertain significance |
| rs149498855 | 19:52,376,806 | T/C | — | likely benign |
| rs752209036 | 19:52,376,875 | C/T | — | likely benign |
| rs544202126 | 19:52,376,908 | C/T | — | uncertain significance |
| rs2084706231 | 19:52,376,950 | A/C | — | uncertain significance |
| rs749959280 | 19:52,376,954 | C/T | — | uncertain significance |
| rs769492914 | 19:52,380,597 | T/C | — | uncertain significance |
| rs1386891677 | 19:52,380,610 | C/A | — | uncertain significance |
| rs189653095 | 19:52,381,664 | G/C | — | uncertain significance |
| rs751857471 | 19:52,381,699 | G/C | — | uncertain significance |
| rs751232642 | 19:52,383,601 | C/T | — | uncertain significance |
| rs11878583 | 19:52,388,546 | A/G | downstream gene variant | — |
| rs192442416 | 19:52,390,901 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.