ZNF507
zinc finger protein 507
Summary
Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in positive regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants65 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs757455419 | 19:32,843,879 | T/C | — | uncertain significance |
| rs2513219189 | 19:32,843,884 | A/G | — | uncertain significance |
| rs756357175 | 19:32,843,924 | G/A | — | uncertain significance |
| rs779352306 | 19:32,843,944 | C/T | — | uncertain significance |
| rs766337650 | 19:32,844,095 | G/A | — | uncertain significance |
| rs745604662 | 19:32,844,151 | G/A | — | uncertain significance |
| rs980418746 | 19:32,844,197 | T/C | — | uncertain significance |
| rs143772508 | 19:32,844,200 | T/C | — | uncertain significance |
| rs1405990916 | 19:32,844,204 | G/C | — | uncertain significance |
| rs752274150 | 19:32,844,208 | T/C | — | uncertain significance |
| rs1345854821 | 19:32,844,215 | G/A | — | uncertain significance |
| rs78467561 | 19:32,844,256 | G/T | — | uncertain significance |
| rs574653667 | 19:32,844,259 | G/T | — | uncertain significance |
| rs749982749 | 19:32,844,349 | A/G | — | uncertain significance |
| rs144710516 | 19:32,844,376 | A/T | — | uncertain significance |
| rs145193065 | 19:32,844,471 | C/T | — | likely benign |
| rs768953538 | 19:32,844,475 | A/G | — | uncertain significance |
| rs148672781 | 19:32,844,597 | C/T | — | likely benign |
| rs373099843 | 19:32,844,632 | C/A | — | uncertain significance |
| rs748383603 | 19:32,844,634 | G/C | — | uncertain significance |
| rs73926019 | 19:32,844,642 | C/A | — | benign |
| rs199551804 | 19:32,844,643 | G/A | — | uncertain significance |
| rs1398005278 | 19:32,844,652 | G/A | — | uncertain significance |
| rs563598774 | 19:32,844,688 | A/G | — | uncertain significance |
| rs547129587 | 19:32,844,733 | T/C | — | uncertain significance |
| rs758919733 | 19:32,844,776 | A/G | — | uncertain significance |
| rs1021739395 | 19:32,844,782 | G/T | — | uncertain significance |
| rs1967209562 | 19:32,844,830 | T/C | — | uncertain significance |
| rs150068736 | 19:32,844,890 | T/G | missense variant | — |
| rs371157788 | 19:32,844,938 | G/A | — | uncertain significance |
| rs12327571 | 19:32,845,032 | G/A | — | benign |
| rs766773762 | 19:32,845,040 | G/A | — | uncertain significance |
| rs753257091 | 19:32,845,132 | G/A | — | uncertain significance |
| rs140268134 | 19:32,845,157 | C/A | — | uncertain significance |
| rs769948845 | 19:32,845,167 | T/G | — | uncertain significance |
| rs953034089 | 19:32,845,252 | A/G | — | uncertain significance |
| rs113433395 | 19:32,845,298 | T/C | — | uncertain significance |
| rs769043344 | 19:32,845,365 | G/T | — | uncertain significance |
| rs147393505 | 19:32,845,419 | C/A | — | uncertain significance |
| rs775293694 | 19:32,845,579 | G/T | — | uncertain significance |
| rs148516792 | 19:32,845,598 | G/A | — | uncertain significance |
| rs368622063 | 19:32,845,652 | G/A | — | uncertain significance |
| rs775247602 | 19:32,845,660 | C/T | — | uncertain significance |
| rs1178539155 | 19:32,845,663 | T/C | — | uncertain significance |
| rs747329123 | 19:32,845,676 | A/G | — | uncertain significance |
| rs2513221695 | 19:32,845,682 | C/G | — | uncertain significance |
| rs143809236 | 19:32,845,727 | G/A | — | uncertain significance |
| rs748761066 | 19:32,845,759 | G/A | — | uncertain significance |
| rs760670719 | 19:32,845,781 | A/G | — | uncertain significance |
| rs1967230988 | 19:32,845,804 | C/T | — | uncertain significance |
| rs61749472 | 19:32,845,848 | A/G | — | benign |
| rs747836526 | 19:32,845,849 | T/C | — | uncertain significance |
| rs1250944117 | 19:32,847,613 | C/G | — | uncertain significance |
| rs376442575 | 19:32,851,484 | A/G | — | uncertain significance |
| rs763392656 | 19:32,851,517 | C/T | — | uncertain significance |
| rs113427979 | 19:32,855,408 | C/A | intron variant | — |
| rs143612000 | 19:32,873,639 | C/G | — | uncertain significance |
| rs113222945 | 19:32,873,640 | C/G | — | uncertain significance |
| rs201200260 | 19:32,873,697 | C/T | — | uncertain significance |
| rs773339789 | 19:32,873,706 | C/T | — | uncertain significance |
| rs561810770 | 19:32,873,802 | G/A | — | uncertain significance |
| rs1967643273 | 19:32,873,834 | A/G | — | likely benign |
| rs769996410 | 19:32,873,849 | G/A | — | uncertain significance |
| rs375411912 | 19:32,873,926 | C/T | — | likely benign |
| rs7248160 | 19:32,874,722 | T/A | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.