{% extends "layout_bs4.html" %} {% from "variants/components.html" import gene_cell, frequency_cell %} {% from "variants/utils.html" import cancer_filters, tier_cell, cell_rank, pagination_footer, pagination_hidden_div %} {% from "variant/buttons.html" import dismiss_variant_table_button %} {% block title %} {{ variant_type|capitalize }} cancer variants {% endblock %} {% block css %} {{ super() }} {% endblock %} {% block top_nav %} {{ super() }}
Rank | Dismiss variant | Gene:Transcript:Exon:HGVS | Tier | Score | Gene | Chr pos | ExAC | Type | Consequence | Tumor | Normal |
---|---|---|---|---|---|---|---|---|---|---|---|
{{cell_rank(variant, institute, case, form, manual_rank_options)}} | {{ dismiss_variant_table_button(variant, institute, case, dismiss_variant_options) }} |
{% for annotation in variant.canonical_transcripts %}
{{ annotation }}
{% endfor %}
|
{{ tier_cell(variant, manual_rank_options, cancer_tier_options) }} | {{ score_cell(variant) }} | {{ gene_cell(variant) }} | {{ position_cell(variant) }} | {{ frequency_cell(variant) }} | {{ variant.sub_category }} |
{% for annotation in variant.functional_annotations %}
{{ annotation }}
{% endfor %}
|
{{ allele_cell(variant.tumor or {}) }} | {{ allele_cell(variant.normal or {}) }} |