Genomics Reporting Implementation Guide
3.0.0 - STU3 International flag

This page is part of the Genetic Reporting Implementation Guide (v3.0.0: STU3) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

Example Observation: molec-conseq2

Generated Narrative: Observation molec-conseq2

status: Final

category: Laboratory, Genetics

code: Molecular Consequence

subject: Alanine B. Everyone Unknown, DoB: 1951-01-20 ( Medical Record Number: m234 (use: usual, ))

effective: 2023-06-01

performer: Organization Some lab

interpretation: Low

derivedFrom: Observation Genetic variant assessment

component

code: coding HGVS

value: NM_001366781.1:c.90T>C

component

code: Transcript reference sequence [ID]

value: NM_001366781.1

component

code: Feature Consequence

value: synonymous_variant