ZNF280D
zinc finger protein 280D
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 DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs199702171 | 15:56,923,700 | C/T | — | uncertain significance |
| rs2548651559 | 15:56,923,787 | A/G | — | uncertain significance |
| rs767680531 | 15:56,923,961 | C/T | — | uncertain significance |
| rs2548651791 | 15:56,923,989 | C/G | — | uncertain significance |
| rs199895235 | 15:56,924,196 | G/C | — | uncertain significance |
| rs201207260 | 15:56,924,219 | G/A | — | uncertain significance |
| rs372725817 | 15:56,924,320 | A/G | — | likely benign |
| rs11857706 | 15:56,939,848 | A/G | intron variant | — |
| rs1478303767 | 15:56,946,418 | G/A | — | uncertain significance |
| rs765723148 | 15:56,946,419 | G/C | — | uncertain significance |
| rs552965807 | 15:56,946,675 | C/T | — | uncertain significance |
| rs767677622 | 15:56,950,640 | T/C | — | uncertain significance |
| rs1274451624 | 15:56,958,626 | C/T | — | uncertain significance |
| rs751081566 | 15:56,958,662 | G/A | — | uncertain significance |
| rs373418547 | 15:56,958,695 | G/T | — | uncertain significance |
| rs772345135 | 15:56,958,707 | A/G | — | uncertain significance |
| rs147594571 | 15:56,958,726 | G/A | — | uncertain significance |
| rs1393265111 | 15:56,958,910 | T/C | — | uncertain significance |
| rs2548713289 | 15:56,959,090 | G/T | — | uncertain significance |
| rs763554281 | 15:56,959,106 | G/A | — | uncertain significance |
| rs2548713355 | 15:56,959,127 | T/C | — | uncertain significance |
| rs375461095 | 15:56,961,075 | G/C | — | uncertain significance |
| rs1257150471 | 15:56,961,104 | T/G | — | uncertain significance |
| rs376630653 | 15:56,968,900 | T/C | — | uncertain significance |
| rs2548734757 | 15:56,968,962 | G/A | — | uncertain significance |
| rs199781890 | 15:56,969,014 | C/T | — | uncertain significance |
| rs772049028 | 15:56,969,832 | A/T | — | uncertain significance |
| rs756056292 | 15:56,974,501 | T/C | — | uncertain significance |
| rs2548751177 | 15:56,974,571 | C/G | — | uncertain significance |
| rs1256387399 | 15:56,974,594 | T/C | — | likely benign |
| rs763234781 | 15:56,974,603 | T/C | — | uncertain significance |
| rs2548751218 | 15:56,974,627 | C/G | — | uncertain significance |
| rs1481650383 | 15:56,974,636 | C/G | — | uncertain significance |
| rs750538277 | 15:56,981,258 | G/A | — | uncertain significance |
| rs918322500 | 15:56,981,280 | T/A | — | uncertain significance |
| rs1195982505 | 15:56,981,310 | G/C | — | uncertain significance |
| rs2056257634 | 15:56,981,331 | T/C | — | uncertain significance |
| rs764235282 | 15:56,981,512 | G/C | — | uncertain significance |
| rs754678266 | 15:56,981,549 | G/T | — | uncertain significance |
| rs1202833147 | 15:56,981,555 | C/T | — | uncertain significance |
| rs2548780995 | 15:56,985,338 | C/T | — | uncertain significance |
| rs760152122 | 15:56,985,385 | A/G | — | uncertain significance |
| rs751032338 | 15:56,993,196 | T/C | — | likely benign |
| rs201400339 | 15:56,993,231 | G/A | — | uncertain significance |
| rs148827203 | 15:56,993,376 | C/T | — | uncertain significance |
| rs2548807904 | 15:56,996,358 | A/C | — | uncertain significance |
| rs201407256 | 15:56,996,429 | T/A | — | uncertain significance |
| rs12910459 | 15:56,998,196 | T/G | — | — |
| rs181694090 | 15:57,006,751 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.