ZNF311
zinc finger protein 311
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 active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2547140637 | 6:28,962,801 | C/T | — | uncertain significance |
| rs140167813 | 6:28,962,932 | C/A | — | uncertain significance |
| rs149909685 | 6:28,962,986 | A/T | — | uncertain significance |
| rs2547191979 | 6:28,963,078 | A/C | — | uncertain significance |
| rs753257964 | 6:28,963,097 | C/G | — | uncertain significance |
| rs369718686 | 6:28,963,142 | C/T | — | likely benign |
| rs1389329526 | 6:28,963,215 | T/G | — | uncertain significance |
| rs756226112 | 6:28,963,296 | C/T | — | uncertain significance |
| rs558888844 | 6:28,963,451 | T/C | — | uncertain significance |
| rs995154602 | 6:28,963,454 | T/C | — | uncertain significance |
| rs754948144 | 6:28,963,486 | G/C | — | uncertain significance |
| rs771754606 | 6:28,963,563 | T/C | — | uncertain significance |
| rs747682785 | 6:28,963,643 | C/T | — | uncertain significance |
| rs2547297644 | 6:28,963,697 | C/T | — | uncertain significance |
| rs539866239 | 6:28,963,716 | C/T | — | uncertain significance |
| rs150967731 | 6:28,963,730 | T/C | — | uncertain significance |
| rs371840973 | 6:28,963,776 | C/T | — | uncertain significance |
| rs2547312790 | 6:28,963,790 | G/C | — | uncertain significance |
| rs750626958 | 6:28,963,835 | C/T | — | uncertain significance |
| rs377545660 | 6:28,963,866 | A/G | — | uncertain significance |
| rs777896975 | 6:28,963,898 | C/A | — | uncertain significance |
| rs754567154 | 6:28,963,911 | G/A | — | uncertain significance |
| rs770152008 | 6:28,963,971 | A/C | — | uncertain significance |
| rs2547357214 | 6:28,964,035 | T/G | — | uncertain significance |
| rs962435173 | 6:28,964,079 | G/A | — | likely benign |
| rs553413861 | 6:28,964,088 | T/C | — | uncertain significance |
| rs1484735211 | 6:28,964,111 | A/C | — | uncertain significance |
| rs1779595323 | 6:28,964,175 | T/G | — | uncertain significance |
| rs1779604230 | 6:28,964,205 | C/G | — | uncertain significance |
| rs114357009 | 6:28,965,512 | G/A | intron variant | — |
| rs763161064 | 6:28,966,556 | C/T | — | uncertain significance |
| rs2150682780 | 6:28,966,565 | C/G | — | uncertain significance |
| rs1780129890 | 6:28,967,273 | C/G | — | uncertain significance |
| rs755196718 | 6:28,967,324 | C/T | — | uncertain significance |
| rs9257452 | 6:28,968,132 | G/A | intron variant | — |
| rs77514138 | 6:28,973,498 | G/T | regulatory region variant | — |
| rs3129794 | 6:28,974,265 | G/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.