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. |
hg clone https://radegast.galaxyproject.org/repos/yusuf/annotate_hgvs
Name | Description | Version | Minimum Galaxy Version |
---|---|---|---|
with deleterious AA and splicing change predictions, protein domain disruptions, etc. | 1.0.0 | any |