ZNF100
zinc finger protein 100
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 Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2512959635 | 19:21,909,495 | A/T | — | uncertain significance |
| rs188037372 | 19:21,909,496 | G/C | — | uncertain significance |
| rs1331615500 | 19:21,909,650 | C/G | — | uncertain significance |
| rs758169696 | 19:21,909,757 | C/T | — | uncertain significance |
| rs1466051835 | 19:21,909,810 | C/G | — | uncertain significance |
| rs368185825 | 19:21,909,817 | C/G | — | uncertain significance |
| rs755146922 | 19:21,909,857 | A/G | — | likely benign |
| rs772418956 | 19:21,909,866 | G/A | — | likely benign |
| rs115256934 | 19:21,909,875 | G/A | — | benign |
| rs200470015 | 19:21,910,084 | G/C | — | uncertain significance |
| rs138292237 | 19:21,910,125 | T/G | — | benign |
| rs565493584 | 19:21,910,228 | T/C | — | uncertain significance |
| rs773362638 | 19:21,910,252 | G/T | — | uncertain significance |
| rs2512962849 | 19:21,910,297 | A/G | — | uncertain significance |
| rs1306847225 | 19:21,910,301 | G/A | — | likely benign |
| rs776757503 | 19:21,910,307 | T/A | — | likely benign |
| rs751670362 | 19:21,910,313 | C/G | — | likely benign |
| rs753189982 | 19:21,910,324 | C/T | — | uncertain significance |
| rs778867351 | 19:21,910,374 | G/A | — | uncertain significance |
| rs376653120 | 19:21,910,434 | T/C | — | uncertain significance |
| rs202116657 | 19:21,910,465 | G/T | — | uncertain significance |
| rs546263430 | 19:21,910,606 | T/C | — | uncertain significance |
| rs370307902 | 19:21,910,623 | T/C | — | uncertain significance |
| rs762849244 | 19:21,910,656 | T/A | — | uncertain significance |
| rs369236200 | 19:21,910,665 | T/A | — | uncertain significance |
| rs199497783 | 19:21,910,683 | T/C | — | uncertain significance |
| rs111519833 | 19:21,910,725 | G/A | — | likely benign |
| rs201183512 | 19:21,910,774 | G/C | — | likely benign |
| rs35717293 | 19:21,912,755 | A/T | — | — |
| rs746401806 | 19:21,926,824 | G/A | — | uncertain significance |
| rs768738116 | 19:21,927,758 | T/G | — | uncertain significance |
| rs778568268 | 19:21,927,787 | T/C | — | uncertain significance |
| rs8102320 | 19:21,936,885 | A/T | — | — |
| rs550860903 | 19:21,948,511 | C/G | — | likely benign |
| rs530281593 | 19:21,948,514 | C/A | — | likely benign |
| rs548577744 | 19:21,948,517 | C/T | — | likely benign |
| rs201163370 | 19:21,948,524 | C/T | — | likely benign |
| rs116085361 | 19:21,948,526 | C/G | — | benign |
| rs6511291 | 19:21,950,402 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.