ZNF350
zinc finger protein 350
Summary
Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II intronic transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nuclear body. Part of transcription repressor complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2278414 | 19:52,467,822 | G/A | 3 prime UTR variant | — |
| rs2514219563 | 19:52,468,120 | G/C | — | uncertain significance |
| rs4988337 | 19:52,468,136 | C/T | — | likely benign |
| rs2278415 | 19:52,468,203 | T/A | missense variant | — |
| rs747308653 | 19:52,468,250 | G/A | — | uncertain significance |
| rs753952350 | 19:52,468,256 | C/T | — | likely benign |
| rs150255847 | 19:52,468,268 | C/T | — | uncertain significance |
| rs115151289 | 19:52,468,327 | G/A | — | benign |
| rs142789660 | 19:52,468,331 | C/T | — | uncertain significance |
| rs370849009 | 19:52,468,378 | C/G | — | uncertain significance |
| rs144263666 | 19:52,468,384 | C/T | — | uncertain significance |
| rs1286592688 | 19:52,468,479 | T/G | — | uncertain significance |
| rs768639393 | 19:52,468,493 | T/C | — | uncertain significance |
| rs150778438 | 19:52,468,501 | T/C | — | uncertain significance |
| rs4988335 | 19:52,468,527 | T/G | — | likely benign |
| rs569458587 | 19:52,468,561 | G/C | — | uncertain significance |
| rs113072853 | 19:52,468,562 | C/T | — | uncertain significance |
| rs3764538 | 19:52,468,587 | G/T | synonymous variant | — |
| rs769439995 | 19:52,468,622 | T/C | — | uncertain significance |
| rs761888276 | 19:52,468,675 | G/A | — | uncertain significance |
| rs2514224026 | 19:52,468,681 | C/T | — | uncertain significance |
| rs2514224088 | 19:52,468,690 | A/C | — | uncertain significance |
| rs781302955 | 19:52,468,777 | C/T | — | uncertain significance |
| rs143609000 | 19:52,468,879 | C/T | — | uncertain significance |
| rs141833873 | 19:52,469,003 | T/C | — | uncertain significance |
| rs757081169 | 19:52,469,062 | A/T | — | uncertain significance |
| rs200481670 | 19:52,469,110 | G/A | — | uncertain significance |
| rs751294011 | 19:52,469,366 | G/T | — | uncertain significance |
| rs754432503 | 19:52,469,371 | A/G | — | uncertain significance |
| rs368232610 | 19:52,469,411 | T/C | — | uncertain significance |
| rs749192272 | 19:52,471,858 | C/T | — | uncertain significance |
| rs1409600848 | 19:52,471,864 | T/C | — | uncertain significance |
| rs199891932 | 19:52,471,908 | G/A | — | uncertain significance |
| rs4987241 | 19:52,472,289 | C/T | missense variant | — |
| rs138898320 | 19:52,472,300 | G/A | missense variant | — |
| rs758411027 | 19:52,472,321 | C/T | — | uncertain significance |
| rs192424319 | 19:52,480,052 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.