Our database stores information of NyuWa resource. It is intregated and specialized for basic information of variant sites. You can input the position range of variant sites in genome, variant IDs or gene names, and then the website will return the results in a short time.
| Variant ID | dbSNP | Region | Gene ID | Exonic function | Consequence | Allele Count | Allele Number | Allele Frequency |
|---|---|---|---|---|---|---|---|---|
rs4986893 | exonic | CYP2C19 | stopgain | CYP2C19:NM_000769.4:exon4:c.G636A:p.W212X | 872 | 21622 | 0.0403 | |
- | intergenic | HLA-DQA1;HLA-DQB1 | - | - | 737 | 19320 | 0.0381 | |
- | intronic | CPNE1 | - | - | 1881 | 20896 | 0.0900 | |
- | intronic | NBEAL1 | - | - | 709 | 20914 | 0.0339 |