This page is part of the Genetic Reporting Implementation Guide (v3.0.0-ballot: STU 3 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. The current version which supersedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions
Generated Narrative: Observation
Resource Observation "MSH2-del-molc"
Profile: Molecular Consequence
status: final
category: Laboratory (Observation Category Codes#laboratory), Genetics (diagnosticServiceSectionId#GE)
code: Molecular Consequence (To Be Determined Codes#molecular-consequence)
subject: Patient/CGPatientExample01 " EVERYMAN"
effective: 2023-02-01
performer: Practitioner/pathologistPractitioner " DOLIN"
derivedFrom: Observation/MSH2-del-var
component
code: coding HGVS (LOINC#48004-6)
value: NM_000251.3:c.1832del (Human Genome Variation Society nomenclature#NM_000251.3:c.1832del)
component
code: Feature Consequence (To Be Determined Codes#feature-consequence)
value: frameshift_variant (sequenceontology.org#SO:0001589)