Genomics Reporting Implementation Guide
3.0.1-SNAPSHOT - Ballot International flag

Genomics Reporting Implementation Guide, published by HL7 International / Clinical Genomics. This guide is not an authorized publication; it is the continuous build for version 3.0.1-SNAPSHOT built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/genomics-reporting/ and changes regularly. See the Directory of published versions

Example Observation: ZFHX3-uncertain-var

Generated Narrative: Observation

ResourceObservation "ZFHX3-uncertain-var"

Profile: Variant

status: final

category: Laboratory (Observation Category Codes#laboratory), Genetics (diagnosticServiceSectionId#GE)

code: Genetic variant assessment (LOINC#69548-6)

subject: Patient/somaticPatient " HAMSBURG"

effective: 2023-02-01

performer: Practitioner/pathologistPractitioner " DOLIN"

value: Present (LOINC#LA9633-4)

method: Sequencing (LOINC#LA26398-0)

component

code: Amino acid change (pHGVS) (LOINC#48005-3)

value: NP_008816.3:p.G585S (Human Genome Variation Society nomenclature#NP_008816.3:p.G585S)

component

code: Transcript reference sequence [ID] (LOINC#51958-7)

value: NM_006885.4 (Gene Reference Sequence Collection#NM_006885.4)

component

code: Allelic read depth (LOINC#82121-5)

value: 212 reads per base pair (Details: UCUM code 1 = '1')

component

code: DNA change (c.HGVS) (LOINC#48004-6)

value: NM_006885.4:c.1753G>A (Human Genome Variation Society nomenclature#NM_006885.4:c.1753G>A)

component

code: Gene studied [ID] (LOINC#48018-6)

value: ZFHX3 (HUGO Gene Nomenclature Committee Genes#HGNC:777)

component

code: Genomic alt allele [ID] (LOINC#69551-0)

value: T

component

code: Chromosome [Identifier] in Blood or Tissue by Molecular genetics method (LOINC#48000-4)

value: Chromosome 16 (LOINC#LA21269-8)

component

code: Genomic allele start-end (LOINC#81254-5)

value: 72992292-72992292

component

code: Genomic reference sequence [ID] (LOINC#48013-7)

value: NC_000016.9 (Gene Reference Sequence Collection#NC_000016.9)

component

code: Genomic ref allele [ID] (LOINC#69547-8)

value: C

component

code: Genomic DNA change (gHGVS) (LOINC#81290-9)

value: NC_000016.9:g.72992292C>T (Human Genome Variation Society nomenclature#NC_000016.9:g.72992292C>T)

component

code: Genomic source class [Type] (LOINC#48002-0)

value: Somatic (LOINC#LA6684-0)

component

code: Sample variant allelic frequency [NFr] (LOINC#81258-6)

value: 0.1 decimal