Create classifications as follows:
Create from existing variant¶
When you click “New Classification” from the allele or variant details page, you are shown a form to pick the transcript and sample:
A number of fields are auto-populated from annotation and sample information (data from VCF record, patient phenotype etc).
Classifications made against a sample are linked from the bottom of the VCF and sample pages.
Variants created from the external API are not auto-populated from annotation.
See the Classification Form.
An administrator can add/remove EvidenceKeys which are used to create fields.
They can also hide visible fields on a per-lab basis.