ZNF705G
zinc finger protein 705G
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 Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1278310802 | 8:7,215,511 | G/A | — | uncertain significance |
| rs184579267 | 8:7,215,514 | G/A | — | uncertain significance |
| rs751096876 | 8:7,215,552 | T/A | — | likely benign |
| rs1323412568 | 8:7,215,616 | C/A | — | uncertain significance |
| rs201738046 | 8:7,215,653 | G/A | — | uncertain significance |
| rs1256572096 | 8:7,215,723 | T/G | — | uncertain significance |
| rs1187960496 | 8:7,215,730 | C/G | — | uncertain significance |
| rs374303145 | 8:7,215,733 | G/A | — | uncertain significance |
| rs1311521354 | 8:7,215,739 | G/A | — | uncertain significance |
| rs548952183 | 8:7,215,746 | C/T | — | uncertain significance |
| rs750547358 | 8:7,215,779 | C/T | — | uncertain significance |
| rs748551083 | 8:7,215,833 | G/T | — | uncertain significance |
| rs368734373 | 8:7,215,835 | C/T | — | uncertain significance |
| rs764090089 | 8:7,215,854 | T/C | — | uncertain significance |
| rs2128834346 | 8:7,215,884 | G/C | — | likely benign |
| rs760498586 | 8:7,215,903 | A/T | — | uncertain significance |
| rs1388641807 | 8:7,215,911 | G/C | — | uncertain significance |
| rs368062945 | 8:7,215,916 | T/C | — | uncertain significance |
| rs374074662 | 8:7,215,936 | A/T | — | uncertain significance |
| rs749481564 | 8:7,215,973 | G/A | — | uncertain significance |
| rs549978063 | 8:7,215,985 | C/T | — | uncertain significance |
| rs775217408 | 8:7,216,039 | G/A | — | likely benign |
| rs762122128 | 8:7,217,158 | A/G | — | uncertain significance |
| rs193060127 | 8:7,217,161 | C/A | — | uncertain significance |
| rs1207837710 | 8:7,217,164 | C/G | — | uncertain significance |
| rs553135197 | 8:7,217,209 | G/A | — | uncertain significance |
| rs377155144 | 8:7,217,221 | T/A | — | uncertain significance |
| rs752127080 | 8:7,217,762 | G/T | — | uncertain significance |
| rs780388285 | 8:7,217,771 | C/G | — | uncertain significance |
| rs201699711 | 8:7,217,774 | G/C | — | uncertain significance |
| rs2486583512 | 8:7,217,834 | A/G | — | uncertain significance |
| rs762616879 | 8:7,217,847 | C/G | — | uncertain significance |
| rs3989699 | 8:7,218,621 | C/G | — | benign |
| rs1806571122 | 8:7,218,671 | C/A | — | uncertain significance |
| rs766409346 | 8:7,218,734 | C/G | — | uncertain significance |
| rs183772362 | 8:7,243,016 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.