697b862c4a5e14cc41f03dfa5757209898c3d5b8
max
  Wed May 21 07:14:40 2025 -0700
triangle decorators for the clinvar track, #35750

diff --git src/hg/utils/otto/clinvar/clinvar.as src/hg/utils/otto/clinvar/clinvar.as
index 1cec731afb2..e16172a9a5b 100644
--- src/hg/utils/otto/clinvar/clinvar.as
+++ src/hg/utils/otto/clinvar/clinvar.as
@@ -26,24 +26,28 @@
     lstring phenotypeList;         "Phenotypes"
     lstring phenotype;         "Phenotype identifiers"
     string origin;         "Allele origin"
     string assembly;         "Genome assembly"
     string cytogenetic;         "Cytogenetic status"
     lstring _jsonHgvsTable;         "HGVS names"
     lstring _hgvsProt;         "Protein HGVS"
     string numSubmit;         "Number of submitters"
     string lastEval;         "Last evaluation"
     string guidelines;         "Guidelines"
     lstring otherIds;         "Other identifiers (ClinGen, OMIM, etc.)"
     lstring _mouseOver;        "Mouse over text"
     string vcfDesc;            "VCF position|Can differ from ClinVar position due to left/right shifting rules"
     string somImpactDesc;       "Somatic Impact"
     string oncogenDesc;       "Oncogen"
+    lstring aggrGermClass;      "Aggregrate Germline Classification"
+    string aggrSomClassImpact;      "Aggregrate Somatic Classification of Clinical Impact"
+    string aggrSomClassOnc;      "Aggregate Somatic Classification of Oncogenicity"
     string _clinSignCode;        "Clinical Significance"
     string _originCode;        "Allele Origin Code"
     string _allTypeCode;        "Variation Type"
     uint _varLen;            "Variant Length in base pairs"
     uint _starCount;         "Number of stars"
     int _variantId;           "ClinVar variant ID"
     string _dbVarSsvId;           "dbVar SSV ID"
     string vcvId;            "ClinVar VCV Accession"
+    string _vcvIdVersion;            "ClinVar VCV with version"
     )