ZNF816
zinc finger protein 816
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 located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1808106 | 19:53,452,944 | T/C | — | — |
| rs138244668 | 19:53,453,091 | C/T | — | uncertain significance |
| rs1348565203 | 19:53,453,109 | T/G | — | uncertain significance |
| rs756641580 | 19:53,453,130 | T/C | — | uncertain significance |
| rs1568435007 | 19:53,453,232 | C/G | — | uncertain significance |
| rs1348042184 | 19:53,453,253 | G/C | — | uncertain significance |
| rs781192258 | 19:53,453,263 | C/T | — | uncertain significance |
| rs1177799321 | 19:53,453,265 | G/C | — | uncertain significance |
| rs878995040 | 19:53,453,295 | C/G | — | likely benign |
| rs777761909 | 19:53,453,414 | T/G | — | uncertain significance |
| rs2083443217 | 19:53,453,485 | C/G | — | uncertain significance |
| rs2514511245 | 19:53,453,491 | C/T | — | uncertain significance |
| rs777890637 | 19:53,453,509 | T/G | — | uncertain significance |
| rs1363419422 | 19:53,453,521 | G/A | — | uncertain significance |
| rs138196750 | 19:53,453,530 | G/C | — | likely benign |
| rs373941419 | 19:53,453,553 | C/T | — | uncertain significance |
| rs754539849 | 19:53,453,645 | A/G | — | likely benign |
| rs775871634 | 19:53,453,657 | T/C | — | likely benign |
| rs201507612 | 19:53,453,733 | T/C | — | uncertain significance |
| rs150225613 | 19:53,453,805 | C/T | — | uncertain significance |
| rs540708659 | 19:53,453,806 | G/A | — | uncertain significance |
| rs758965064 | 19:53,453,820 | T/G | — | uncertain significance |
| rs780618606 | 19:53,453,862 | A/G | — | uncertain significance |
| rs762936794 | 19:53,453,878 | G/C | — | uncertain significance |
| rs138017999 | 19:53,453,880 | G/A | missense variant | — |
| rs759357555 | 19:53,453,885 | T/C | — | likely benign |
| rs999358382 | 19:53,453,922 | T/C | — | uncertain significance |
| rs999157262 | 19:53,453,934 | C/T | — | uncertain significance |
| rs2514513075 | 19:53,453,992 | A/G | — | uncertain significance |
| rs771801043 | 19:53,453,996 | A/C | — | uncertain significance |
| rs775347581 | 19:53,454,000 | C/T | — | uncertain significance |
| rs143850515 | 19:53,454,034 | G/A | — | likely benign |
| rs753119579 | 19:53,454,039 | C/T | — | uncertain significance |
| rs140118973 | 19:53,454,087 | T/C | — | likely benign |
| rs367840821 | 19:53,454,225 | T/C | — | uncertain significance |
| rs147910359 | 19:53,454,321 | T/C | — | uncertain significance |
| rs79991347 | 19:53,454,370 | G/A | — | likely benign |
| rs752633968 | 19:53,454,447 | C/T | — | uncertain significance |
| rs138373839 | 19:53,454,499 | T/G | — | uncertain significance |
| rs572629673 | 19:53,454,529 | G/A | — | uncertain significance |
| rs561934343 | 19:53,454,618 | C/T | — | uncertain significance |
| rs529254404 | 19:53,454,623 | C/G | — | uncertain significance |
| rs139245005 | 19:53,454,654 | T/C | — | uncertain significance |
| rs770177847 | 19:53,454,677 | C/A | — | uncertain significance |
| rs8111196 | 19:53,457,223 | A/G | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.