{% extends "layout.html" %} {% from "clinvar/components.html" import condition_identifiers, hgvs_choices, observations %} {% block css %} {{ super() }} {% endblock %} {% block title %} {{ super() }} - {{ institute.display_name }} {% endblock %} {% block top_nav %} {{ super() }} {% endblock %} {% block content %} {% if variant_data.var_obj.category in ["snv", "cancer"]%} {% set var_category = 'snv' %} {% else %} {% set var_category = 'sv' %} {% endif %}
  • Start
  • Germline Classification
  • Variant Details
  • Inheritance Model
  • Associated conditions
  • Observation Data
ClinVar variant submission form

The form present on this page mirrors the fields on the ClinVar submission spreadsheets.
After collecting the required fields, this variant gets saved in an open ClinVar submission object.

Germline Classification {{ variant_data.var_form.csrf_token }} {{ variant_data.var_form.case_id() }} {{ variant_data.var_form.category() }} {{ variant_data.var_form.local_id() }} {{ variant_data.var_form.linking_id() }} {{ variant_data.var_form.ref() }} {{ variant_data.var_form.alt() }} {{ variant_data.var_form.assembly() }} {% if var_category == 'snv' %} {{ variant_data.var_form.chromosome() }} {{ variant_data.var_form.start() }} {{ variant_data.var_form.stop() }} {% endif %}

{% set scout_classif = variant_data.var_obj.classification|replace("_"," ") if variant_data.var_obj.classification else "n.a." %} {{variant_data.var_form.classification.label(class="fw-bold, text-dark")}} *


{{ variant_data.var_form.last_evaluated.label(class="fw-bold, text-dark") }} {{ variant_data.var_form.last_evaluated(class="bg-white") }}
{{ variant_data.var_form.clinsig_comment.label(class="fw-bold, text-dark") }} * {{ variant_data.var_form.clinsig_comment(rows=4, class="bg-white") }}


{{ variant_data.var_form.assertion_method_cit_db.label(class="fw-bold, text-dark") }} {{ variant_data.var_form.assertion_method_cit_db(class="form-control, btn-secondary") }} ? *
{{ variant_data.var_form.assertion_method_cit_id.label( class="fw-bold, text-dark", id="citation_tooltip", **{'data-bs-toggle': 'tooltip', 'title': 'Original tooltip text'} ) }} {{ variant_data.var_form.assertion_method_cit_id(class="bg-white") }}
Variant Details {{variant_data.var_form.gene_symbol.label(class="fw-bold, text-dark")}} ? {{variant_data.var_form.gene_symbol(class="bg-white")}}
{% if var_category == 'snv' %}

{{hgvs_choices(variant_data.var_form.tx_hgvs)}}

{{variant_data.var_form.variations_ids.label(class="fw-bold, text-dark")}} {{variant_data.var_form.variations_ids(class="bg-white")}}
{% else %} {{ variant_data.var_form.length() }}
{{ variant_data.var_form.var_type.label( class="fw-bold text-dark d-inline-block", style="width: 180px;" ) }} {{ variant_data.var_form.var_type( class="form-control d-inline-block btn-secondary", style="width: 200px;" ) }}

{{ variant_data.var_form.ref_copy.label( class="fw-bold text-dark d-inline-block", style="width: 180px;" ) }} {{ variant_data.var_form.ref_copy( size=5, class="bg-white w-auto", style="width: 100px;" ) }}

{{ variant_data.var_form.ncopy.label( class="fw-bold text-dark d-inline-block", style="width: 180px;" ) }} ? {{ variant_data.var_form.ncopy( size=5, class="bg-white w-auto", style="width: 100px;" ) }}

{{ variant_data.var_form.chromosome.label( class="fw-bold text-dark d-inline-block", style="width: 180px;" ) }} {{ variant_data.var_form.chromosome( size=5, class="bg-white d-inline-block", style="width: 100px;" ) }}

Coordinates
{{ variant_data.var_form.breakpoint1.label(class="fw-bold text-dark me-2") }} {{ variant_data.var_form.breakpoint1(class="bg-white", style="width: 300px;") }}

{{ variant_data.var_form.breakpoint2.label(class="fw-bold text-dark me-2") }} {{ variant_data.var_form.breakpoint2(class="bg-white", style="width: 300px;") }}
{{ variant_data.var_form.outer_start.label(class="fw-bold text-dark me-2") }} {{ variant_data.var_form.outer_start( size=20, class="bg-white", style="width: 300px;" ) }}

{{ variant_data.var_form.inner_start.label(class="fw-bold text-dark me-2") }} {{ variant_data.var_form.inner_start( size=20, class="bg-white", style="width: 300px;" ) }}

{{ variant_data.var_form.inner_stop.label(class="fw-bold text-dark me-2") }} {{ variant_data.var_form.inner_stop( size=20, class="bg-white", style="width: 300px;" ) }}

{{ variant_data.var_form.outer_stop.label(class="fw-bold text-dark me-2") }} {{ variant_data.var_form.outer_stop( size=20, class="bg-white", style="width: 300px;" ) }}
{% endif %}
Inheritance model

The mode of inheritance specific to the variant-disease pair, not generally for the disease

{{variant_data.var_form.inheritance_mode.label(class="fw-bold, text-dark")}} {{variant_data.var_form.inheritance_mode(class="form-control, btn-secondary")}}
Associated Conditions

The condition for which the variant is interpreted. Examples available at ClinVar

{{ condition_identifiers(variant_data.var_form) }}
Observation Data

Information provided by filling in these fields will be used to create the CaseData.csv file. Observations from at least one individuals are required.

{{ observations(variant_data.cdata_forms) }}
{% endblock %} {% block scripts %} {{ super() }} {% include "clinvar/scripts.html" %} {% endblock %}