CUL4A
cullin 4A
Summary
CUL4A is the ubiquitin ligase component of a multimeric complex involved in the degradation of DNA damage-response proteins (Liu et al., 2009 [PubMed 19481525]).[supplied by OMIM, Oct 2009]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2503851345 | 13:113,863,988 | G/A | — | uncertain significance |
| rs1163049031 | 13:113,864,044 | G/C | — | uncertain significance |
| rs953495267 | 13:113,864,054 | G/A | — | uncertain significance |
| rs866449815 | 13:113,864,087 | G/A | — | uncertain significance |
| rs1455037982 | 13:113,864,314 | C/G | — | uncertain significance |
| rs761690889 | 13:113,864,394 | C/G | — | uncertain significance |
| rs35306827 | 13:113,869,045 | G/A | intron variant | — |
| rs7985335 | 13:113,869,244 | G/A | — | — |
| rs35569628 | 13:113,872,712 | T/G | — | — |
| rs1379704929 | 13:113,873,353 | C/T | — | uncertain significance |
| rs9549698 | 13:113,877,701 | A/G | intron variant | — |
| rs7999579 | 13:113,879,357 | T/C | intron variant | — |
| rs767080315 | 13:113,883,767 | T/A | — | uncertain significance |
| rs147136485 | 13:113,887,517 | C/T | — | uncertain significance |
| rs761560555 | 13:113,887,540 | G/A | — | uncertain significance |
| rs376759372 | 13:113,887,544 | A/G | — | uncertain significance |
| rs369257799 | 13:113,887,594 | G/A | — | uncertain significance |
| rs2504084551 | 13:113,888,245 | A/G | — | uncertain significance |
| rs9549705 | 13:113,888,425 | T/C | intron variant | — |
| rs56119221 | 13:113,888,721 | C/G | intron variant | — |
| rs2041496661 | 13:113,889,452 | A/G | — | likely benign |
| rs766324333 | 13:113,897,283 | C/G | — | uncertain significance |
| rs375774505 | 13:113,897,303 | A/G | — | uncertain significance |
| rs1223000474 | 13:113,900,284 | G/T | — | uncertain significance |
| rs1481932865 | 13:113,900,300 | A/G | — | uncertain significance |
| rs138665383 | 13:113,900,349 | C/T | — | uncertain significance |
| rs114695232 | 13:113,904,818 | A/G | intron variant | — |
| rs779528054 | 13:113,909,098 | T/C | — | uncertain significance |
| rs182629653 | 13:113,912,420 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.