Repository annotate_hgvs
Owner: yusuf
Synopsis: with deleterious AA and splicing change predictions, protein domain disruptions, etc.
This tool reports several functional attributes, and potential for functional disturbance, based on genes that have declared sequence variants. These results can be used to help find the genetic cause of a clinical phenotype.
Type: unrestricted
Revision: 0:9977d1935a07
This revision can be installed: True
Times cloned / installed: 145

Contents of this repository

Name Description Version Minimum Galaxy Version
with deleterious AA and splicing change predictions, protein domain disruptions, etc. 1.0.0 any