Dear all, I am working on a database of several patients with relative variants (SNV and INDELS basically) VCF files. I know I can check for variant effect against VEP DB or similar, but for variants that are absent in such databases, how can I possibly categorize them in effect result? (e.g. missense vs nonsense etc)
Thanks a lot in advance for any help!
Pretty sure VEP will still tell you whether it's missense or nonsense even if it isn't a known variant. snpEff is another option that provides a wide breadth of output.
Thanks a lot for your reply! Do you know if they have downloadable DBs in to retrieve this information from? in order to automatized the annotation through a script?
http://snpeff.sourceforge.net/download.html#databases