DCAF4
DDB1 and CUL4 associated factor 4
Summary
This gene encodes a WD repeat-containing protein that interacts with the Cul4-Ddb1 E3 ligase macromolecular complex. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2009]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17182090 | 14:73,392,096 | C/T | regulatory region variant | — |
| rs12587742 | 14:73,393,391 | G/A | regulatory region variant | — |
| rs76891117 | 14:73,399,837 | A/G | upstream gene variant | — |
| rs751470383 | 14:73,404,702 | T/C | — | uncertain significance |
| rs151012011 | 14:73,404,707 | G/C | — | uncertain significance |
| rs540271702 | 14:73,404,718 | G/A | — | uncertain significance |
| rs780835122 | 14:73,404,763 | G/A | — | likely benign |
| rs17122598 | 14:73,404,770 | T/C | — | benign |
| rs752065571 | 14:73,406,577 | T/G | — | uncertain significance |
| rs1567305296 | 14:73,407,000 | A/G | — | uncertain significance |
| rs750942030 | 14:73,407,024 | G/A | — | likely benign |
| rs149878526 | 14:73,407,032 | G/A | — | uncertain significance |
| rs373770788 | 14:73,407,053 | C/T | — | uncertain significance |
| rs145062084 | 14:73,407,054 | G/A | — | likely benign |
| rs1567305536 | 14:73,407,066 | A/G | — | uncertain significance |
| rs2504090239 | 14:73,408,461 | G/C | — | uncertain significance |
| rs2240980 | 14:73,409,683 | C/G | regulatory region variant | — |
| rs200407119 | 14:73,409,755 | G/A | — | likely benign |
| rs748595467 | 14:73,412,611 | G/A | — | uncertain significance |
| rs141191522 | 14:73,412,626 | A/C | — | uncertain significance |
| rs755541492 | 14:73,412,731 | G/A | — | uncertain significance |
| rs2246976 | 14:73,412,739 | C/A | splice region variant | — |
| rs2504144538 | 14:73,413,851 | T/C | — | uncertain significance |
| rs114910738 | 14:73,414,561 | G/T | intron variant | — |
| rs2806041 | 14:73,414,895 | G/T | intron variant | — |
| rs2535913 | 14:73,415,233 | G/A | — | uncertain significance |
| rs72734407 | 14:73,416,576 | C/G | intron variant | — |
| rs137901416 | 14:73,418,095 | G/A | intron variant | — |
| rs767937789 | 14:73,418,522 | C/T | — | uncertain significance |
| rs758181303 | 14:73,418,573 | A/C | — | uncertain significance |
| rs755032980 | 14:73,420,913 | G/A | — | uncertain significance |
| rs779012938 | 14:73,420,916 | G/T | — | uncertain significance |
| rs139579806 | 14:73,420,925 | T/G | — | uncertain significance |
| rs778257059 | 14:73,420,935 | C/G | — | uncertain significance |
| rs142503309 | 14:73,421,103 | G/A | — | uncertain significance |
| rs752860092 | 14:73,421,108 | G/A | — | uncertain significance |
| rs150517676 | 14:73,421,150 | G/A | — | uncertain significance |
| rs117449182 | 14:73,421,159 | A/G | — | likely benign |
| rs2504240644 | 14:73,422,277 | T/C | — | uncertain significance |
| rs535665448 | 14:73,422,286 | G/A | — | uncertain significance |
| rs141315052 | 14:73,422,322 | G/A | — | uncertain significance |
| rs140598805 | 14:73,423,127 | G/A | — | likely benign |
| rs776853264 | 14:73,423,134 | A/C | — | uncertain significance |
| rs373000336 | 14:73,423,139 | G/A | — | uncertain significance |
| rs1384431721 | 14:73,423,175 | C/T | — | uncertain significance |
| rs147302871 | 14:73,425,328 | G/A | — | uncertain significance |
| rs143869522 | 14:73,425,365 | G/A | — | benign |
| rs367672481 | 14:73,425,389 | C/T | — | uncertain significance |
| rs781639820 | 14:73,425,437 | G/C | — | uncertain significance |
| rs146493974 | 14:73,425,457 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.