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. For a full list of available versions, see the Directory of published versions
Generated Narrative: Observation molec-conseq3
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: Modifier
derivedFrom: Observation Genetic variant assessment
component
code: coding HGVS
value: NM_001395543.1:c.-171T>C
component
code: Transcript reference sequence [ID]
value: NM_001395543.1
component
code: Feature Consequence
value: 5_prime_UTR_variant