Philips ISPM Aberration
The table onc_philips_mtb_aberrations contains genomic testing information from the Philips IntelliSpace Precision Medicine (ISPM) genomics database at Stanford. The fields in this table are related to genomic testing details about each sample, as well as the specimen accession number which can be used to link to the Philips ISPM Orders table.
Table Columns
| column name | type | phi | phi-scrubbing operation |
|---|---|---|---|
| aberration_class | STRING | ||
| aberration_type | STRING | ||
| accession_number | STRING | Yes | Hash |
| chrom | STRING | ||
| hgnc_gene | STRING | ||
| id | STRING | Yes | Stable Between Data Refreshes |
| is_selected_aberration_flag | INT64 | ||
| person_id | INT64 | Yes | Stable Between Data Refreshes |
| stanford_aa_change | STRING | ||
| stanford_break_1 | STRING | ||
| stanford_break_2 | STRING | ||
| stanford_gene | STRING | ||
| stanford_hgvs_coding | STRING | ||
| stanford_hgvs_genomic | STRING | ||
| stanford_hgvs_protein | STRING | ||
| stanford_interpretation | STRING | Yes | TiDE |
| stanford_minimum_copies | STRING | ||
| stanford_pathogenicity | STRING | ||
| stanford_patient_uid | STRING | Yes | Del |
| stanford_region_1 | STRING | ||
| stanford_transcript | STRING | ||
| stanford_vaf | STRING | ||
| stanford_variant | STRING |
Columns Description
aberration_class
Aberration class (No description available)
aberration_type
Aberration type (No description available)
accession_number
Identifier for the specimen. This field can be used to link to the pat_diag_orders table. Note that there can be multiple records with the same accession number.
chrom
The chromosome number that the gene impacted by the aberration is located on (No description available)
hgnc_gene
The HUGO Gene Nomenclature Committee (HGNC)-approved name for the gene impacted by the aberration (No description available)
id
Primary Key for aberrations table (No description available)
is_selected_aberration_flag
Flag indicating if the aberration record is a “selected aberration” (id is in the selected_aberrations staging table).
person_id
Person_id as corresponds to the OMOP dataset
stanford_aa_change
Amino acid (AA) change as reported in the Stanford STAMP results report. First letter indicates the amino acid impacted, indicated by its one-letter code, then a series of numbers which indicate the position of the amino acid within the protein sequence, then a string abbreviation which denotes the type of mutation (example - G646fs is a frameshift mutation occurring at the amino acid Glycine, position 646 within the protein sequence for the protein encoded by the impacted ASXL1 gene). (No description available)
stanford_break_1
No description available. This field is not well-populated.
stanford_break_2
No description available. This field is not well-populated.
stanford_gene
Gene impacted by the aberration, as reported in the Stanford STAMP results report. (No description available)
stanford_hgvs_coding
Standardized HGVS nomenclature representation for the variants in the coding DNA sequence of a gene, as reported in the Stanford STAMP results report (No description available)
stanford_hgvs_genomic
Standardized HGVS nomenclature representation for the variants in the genomic sequence of a chromosome, as reported in the Stanford STAMP results report (No description available)
stanford_hgvs_protein
Standardized HGVS nomenclature representation for the variants in the protein sequence, as reported in the Stanford STAMP results report (No description available)
stanford_interpretation
Text field containing interpretation of the aberration found, as reported in the Stanford STAMP results report (No description available)
stanford_minimum_copies
No description available. This field is not well-populated.
stanford_pathogenicity
Pathogenicity level of the aberration (No description available)
stanford_patient_uid
Internal Stanford tracking ID (this is the patient’s MRN | DOB)
stanford_region_1
No description available. This field is not well-populated.
stanford_transcript
No description available.
stanford_vaf
Variant allele frequency (VAF), as reported in the Stanford STAMP results report (No description available)
stanford_variant
Full variant the aberration causes, as reported in the Stanford STAMP results report (No description available)