DPF3
double PHD fingers 3
Summary
This gene encodes a member of the D4 protein family. The encoded protein is a transcription regulator that binds acetylated histones and is a component of the BAF chromatin remodeling complex. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2526932 | 14:73,081,068 | A/C | — | — |
| rs2503240911 | 14:73,137,870 | T/C | — | uncertain significance |
| rs1886660226 | 14:73,137,928 | C/G | — | uncertain significance |
| rs762501809 | 14:73,137,989 | G/A | — | uncertain significance |
| rs2503241503 | 14:73,138,011 | C/A | — | uncertain significance |
| rs139401957 | 14:73,140,945 | C/A | splice region variant | — |
| rs368158261 | 14:73,140,966 | C/T | — | uncertain significance |
| rs771502693 | 14:73,140,990 | G/A | — | uncertain significance |
| rs1411834661 | 14:73,141,008 | T/A | — | uncertain significance |
| rs376577589 | 14:73,141,010 | T/C | — | uncertain significance |
| rs368974268 | 14:73,141,064 | G/A | — | uncertain significance |
| rs10129954 | 14:73,150,701 | C/T | intron variant | — |
| rs367710148 | 14:73,152,486 | T/A | — | — |
| rs1318429711 | 14:73,159,849 | T/A | — | uncertain significance |
| rs2503337985 | 14:73,181,146 | G/A | — | uncertain significance |
| rs200602274 | 14:73,181,153 | G/T | — | uncertain significance |
| rs369816936 | 14:73,181,203 | C/T | — | uncertain significance |
| rs762349851 | 14:73,181,206 | G/A | — | uncertain significance |
| rs1313292844 | 14:73,190,343 | G/A | — | uncertain significance |
| rs2503360016 | 14:73,190,433 | C/T | — | uncertain significance |
| rs752921327 | 14:73,198,518 | T/C | — | uncertain significance |
| rs11158975 | 14:73,203,918 | C/G | — | — |
| rs772716056 | 14:73,220,002 | G/C | — | uncertain significance |
| rs769634317 | 14:73,220,004 | T/A | — | uncertain significance |
| rs3742836 | 14:73,220,020 | A/G | — | benign |
| rs369823716 | 14:73,220,035 | G/A | — | uncertain significance |
| rs772329830 | 14:73,238,480 | T/C | — | uncertain significance |
| rs199742673 | 14:73,238,525 | C/T | — | uncertain significance |
| rs2503484692 | 14:73,238,558 | T/G | — | uncertain significance |
| rs2503484817 | 14:73,238,594 | C/T | — | uncertain significance |
| rs74884082 | 14:73,249,419 | C/T | intron variant | — |
| rs11621358 | 14:73,263,634 | G/A | intron variant | — |
| rs4606656 | 14:73,281,432 | C/T | intron variant | — |
| rs147478227 | 14:73,323,393 | C/T | upstream gene variant | — |
| rs35020117 | 14:73,341,655 | T/A | — | — |
| rs8007139 | 14:73,346,100 | A/G | intron variant | — |
| rs759283 | 14:73,356,307 | C/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.