1942abfbe86d5b3f5ed3ad0482a31a9354587e18 max Tue Mar 26 09:30:03 2024 -0700 preparing clinvar for somatic mutations, no ticket yet diff --git src/hg/utils/otto/clinvar/clinvarSub.sql src/hg/utils/otto/clinvar/clinvarSub.sql new file mode 100644 index 0000000..bb3aa5c --- /dev/null +++ src/hg/utils/otto/clinvar/clinvarSub.sql @@ -0,0 +1,25 @@ +# clinvarSub.sql was originally generated by the autoSql program, which also +# generated clinvarSub.c and clinvarSub.h. This creates the database representation of +# an object which can be loaded and saved from RAM in a fairly +# automatic way. + +#ClinVar variant submission info +CREATE TABLE clinvarSub ( + varId int not null, # the identifier assigned by ClinVar and used to build the URL, namely https://ncbi.nlm.nih.gov/clinvar/VariationID + clinSign varchar(255) not null, # interpretation of the variation-condition relationship + dateLastEval varchar(255) not null, # the last date the variation-condition relationship was evaluated by this submitter + description longblob not null, # an optional free text description of the basis of the interpretation + subPhenoInfo longblob not null, # the name(s) or identifier(s) submitted for the condition that was interpreted relative to the variant + repPhenoInfo longblob not null, # the MedGen identifier/name combinations ClinVar uses to report the condition that was interpreted. 'na' means there is no public identifer in MedGen for the condition. + revStatus varchar(255) not null, # the level of review for this submission, namely http//www.ncbi.nlm.nih.gov/clinvar/docs/variation_report/#review_status + collMethod varchar(255) not null, # the method by which the submitter obtained the information provided + originCounts varchar(255) not null, # origin and the number of observations for each origin + submitter varchar(255) not null, # the submitter of this record + scv varchar(255) not null, # the accession and current version assigned by ClinVar to the submitted interpretation of the variation-condition relationship + subGeneSymbol varchar(255) not null, # the gene symbol reported in this record + explOfInterp longblob not null, # more details if ClinicalSignificance is 'other' or 'drug response' + somClinImpact longblob not null, # the somatic classification of clinical impact on this submitted record + oncogenicity varchar(255) not null, # the somatic classification of oncogenicity on this submitted record + #Indices + INDEX(varId) +);