ZNF300
zinc finger protein 300
Summary
The protein encoded by this gene is a C2H2-type zinc finger DNA binding protein and likely transcriptional regulator. The function of this protein is not yet known. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs942904034 | 5:150,275,144 | C/T | — | uncertain significance |
| rs147702441 | 5:150,275,179 | C/T | — | uncertain significance |
| rs754022980 | 5:150,275,226 | T/G | — | uncertain significance |
| rs201176485 | 5:150,275,254 | G/A | — | uncertain significance |
| rs866282218 | 5:150,275,315 | T/G | — | uncertain significance |
| rs554976762 | 5:150,275,374 | C/T | — | uncertain significance |
| rs372607730 | 5:150,275,407 | T/A | — | uncertain significance |
| rs376308554 | 5:150,275,434 | T/A | — | uncertain significance |
| rs566492867 | 5:150,275,528 | T/C | — | uncertain significance |
| rs575599619 | 5:150,275,641 | C/T | — | uncertain significance |
| rs746103177 | 5:150,275,726 | C/T | — | uncertain significance |
| rs148013564 | 5:150,275,727 | G/A | — | benign |
| rs1378958213 | 5:150,275,743 | T/C | — | uncertain significance |
| rs576694189 | 5:150,275,854 | T/C | — | uncertain significance |
| rs1754776974 | 5:150,275,876 | T/G | — | uncertain significance |
| rs796140472 | 5:150,275,902 | C/T | — | uncertain significance |
| rs2531922272 | 5:150,275,963 | T/C | — | uncertain significance |
| rs1385237648 | 5:150,275,972 | C/T | — | uncertain significance |
| rs375500246 | 5:150,276,032 | T/G | — | uncertain significance |
| rs745625061 | 5:150,276,041 | G/T | — | uncertain significance |
| rs766855152 | 5:150,276,089 | C/T | — | uncertain significance |
| rs143725595 | 5:150,276,111 | A/G | — | benign |
| rs148132991 | 5:150,276,152 | C/T | — | benign |
| rs368888702 | 5:150,276,161 | G/C | — | likely benign |
| rs148747180 | 5:150,276,199 | G/A | — | uncertain significance |
| rs969362824 | 5:150,276,282 | C/G | — | uncertain significance |
| rs142975240 | 5:150,276,288 | A/C | — | benign |
| rs779916263 | 5:150,276,449 | C/T | — | uncertain significance |
| rs1367158911 | 5:150,276,452 | T/C | — | uncertain significance |
| rs372902064 | 5:150,276,502 | C/T | — | uncertain significance |
| rs11741861 | 5:150,277,909 | A/G | intron variant | — |
| rs2531931624 | 5:150,278,056 | C/G | — | uncertain significance |
| rs4958427 | 5:150,278,587 | C/T | intron variant | — |
| rs368281057 | 5:150,282,738 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.