BE-FF Database

The BE-FF database contains analyzed data of human pathogenic SNVs from NCBI dbSNP. For each represented point mutation in the database, BE-FF found a possible base editing correction.

The positive results are indicated as ‘Precise’ or ‘Synonymous’ corrections under the relevant base editor. SNPs that do not appear in the database are not necessarily incompatible for base editing, they might not be included in the original dataset as well. Please check the “Original_dataset.csv” file to find whether your mutation of interest appears in it or not, in case it can’t be found in the BE-FF db.