Single nucleotide variant

Question

[heureuse]

Hello, I would like to know if there is a method/pipeline that help to retrieve all single nucleotide variant in human genome that lead to a loss of function . Thanks.

Answer 1

[Pierre Lindenbaum]

https://sites.google.com/site/jpopgen/dbNSFP

dbNSFP is a database developed for functional prediction and annotation of all potential non-synonymous single-nucleotide variants (nsSNVs) in the human genome. I

[heureuse]

Thanks a lot