Browse disease-related SNVs were mapped to modification sites/regions, extended by an additional 10 nt in both the 5′- and 3′-directions for each modification site.
Our research on analysis of RNA modifications and single-nucleotide variations (SNVs) discovered over 100 diseases may associated with RNA modifications.
1. Displays disease-related SNVs were mapped to modification sites/regions.
2. The user can also click on the title of the table to sort RNA modification sites according to various features, such as modId, modType, SNPid, disease, the gene names or the gene types.
3. The number in the relPos column represents the offset of SNP loci relative to the modification site.
4. A negative number means the SNP appears in the upstream of the modification site and positive means downstream.