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
Generated Narrative: Observation STAG2-insertion-molc
status: Final
category: Laboratory, Genetics
code: Molecular Consequence
subject: Adam B. Everyman Male, DoB: 1951-01-20 ( Medical Record Number: m123 (use: usual, ))
effective: 2023-02-01
performer: Practitioner Test Dolin
derivedFrom: Observation Genetic variant assessment
component
code: coding HGVS
value: NM_006603.5:c.3530_3531insGTGACTATTAATAT
component
code: Transcript reference sequence [ID]
value: NM_006603.5
component
code: Feature Consequence
value: frameshift_variant
component
code: Amino acid change (pHGVS)
value: NP_006594.3:p.S1178*