S2A. NoDupsNonFunc—de-duplicated set of mutations from all samples of the dataset; non-functional. S2B. NoDupsFunc—de-duplicated set of mutations from all samples of the dataset; aminoacid changes or
MaveDB is an open-access, community-curated repository that currently hosts > 7 million experimentally measured variant-effect scores from > 1 000 multiplexed assays of variant effect (MAVEs). It prov
a SNVs that were predicted by both dmax and rmin measures are highlighted with †. b The p-value corresponding to the rmin measure is highlighted with *. c The conserved RNA secondary structure predict
This file is the output file of Ensembl's Variant Effect Predictor run on genic variants observed in 107 wolves at a minimum call rate of 95%. See main text for more details.
