DVA prediction scores

Here, we provide the DVA prediction scores of s missense variants that were extracted from ClinVar, Varibench, COSMIC, and VariSNP databases. (Genome assembly: GRCh37/hg19). You can download them using the following links:

Somatic cancer missense variants: Here

The missense variants in the ClinVar database: Here

The missense variants in the VariBench database: Here

License

If you are using DVA in your academic study, please cite our paper.
If you want to use DVA in a commercial application, you should contact us for permission.