{
  "variants": [
    "variant_idx",
    "gene_symbol",
    "chromosome",
    "position",
    "reference_allele",
    "alternate_allele",
    "genome_build",
    "rsid",
    "spliceai_max_score",
    "bayesdel_noaf_score",
    "bayesdel_noaf_pred",
    "bayesdel_addaf_score",
    "bayesdel_addaf_pred",
    "mpc_score",
    "consequence",
    "impact",
    "hgvs_protein",
    "hgvs_cdna",
    "acmg_class",
    "acmg_criteria",
    "confidence_score",
    "priority_score",
    "global_af",
    "clinical_significance",
    "genotype",
    "depth",
    "quality",
    "allelic_depth",
    "processing_notes",
    "classification_snapshot_id",
    "acmg_rule_evidence",
    "filter_status",
    "filter_status_is_original",
    "filters",
    "pass_quality_filter",
    "nuclear_pm1_evidence_source",
    "alphamissense_score",
    "sift_score",
    "pipeline_flagged",
    "pipeline_flag_reason",
    "nuclear_de_novo_candidate",
    "nuclear_de_novo_upgrade_class",
    "pli",
    "nuclear_erepo_assertion",
    "nuclear_erepo_panel",
    "nuclear_erepo_disease",
    "nuclear_erepo_summary",
    "nuclear_erepo_link",
    "classification_framework",
    "mmdwg_module_version",
    "mmdwg_heteroplasmy",
    "mmdwg_heteroplasmy_source",
    "mmdwg_predicted_haplogroup",
    "mmdwg_haplogroup_confidence",
    "mt_ps2_evidence",
    "mt_ps3_evidence",
    "mt_ps4_proband_count",
    "mt_ps4_haplogroup_diversity_count",
    "mt_pm6_evidence",
    "mt_pp1_maternal_member_count",
    "mt_pp1_heteroplasmy_correlation",
    "mt_pp1_homoplasmic_in_all",
    "mt_pp4_etc_deficiency",
    "mt_bs2_evidence",
    "mt_bs3_evidence",
    "mt_bs4_evidence",
    "mt_bp5_evidence",
    "mt_ps2_strength",
    "mt_pm6_strength",
    "mt_bs2_strength"
  ],
  "phenotype_matches": [
    "variant_idx",
    "gene_symbol",
    "phenotype_match_score",
    "matched_terms",
    "total_patient_terms",
    "total_variant_terms",
    "clinical_priority_score",
    "clinical_tier",
    "acmg_class",
    "impact",
    "global_af",
    "consequence",
    "individual_matches",
    "demotion_reason",
    "inheritance_note"
  ],
  "screening_results": [
    "variant_idx",
    "screening_tier",
    "total_score",
    "clinical_actionability",
    "acmg_boost",
    "phenotype_boost",
    "ethnicity_boost",
    "family_history_boost",
    "de_novo_boost",
    "constraint_score",
    "deleteriousness_score",
    "phenotype_score",
    "dosage_score",
    "consequence_score",
    "compound_het_score",
    "age_relevance_score",
    "age_group",
    "screening_mode",
    "justification",
    "screened_at",
    "disease_name_panel",
    "display_label",
    "clingen_status"
  ],
  "literature_results": [
    "pmid",
    "title",
    "abstract",
    "journal",
    "publication_date",
    "authors",
    "doi",
    "pmc_id",
    "relevance_score",
    "phenotype_score",
    "publication_type_score",
    "gene_centrality_score",
    "functional_data_score",
    "variant_score",
    "recency_score",
    "gene_mentions",
    "variant_matches",
    "phenotype_matches",
    "has_exact_variant",
    "has_functional_data",
    "publication_type",
    "max_gene_mentions",
    "evidence_strength",
    "searched_at"
  ]
}