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 "RepeatExpansion"
Profile: Variant
status: final
category: Laboratory (Observation Category Codes#laboratory), Genetics (diagnosticServiceSectionId#GE)
code: Genetic variant assessment (LOINC#69548-6)
subject: Patient/ExamplePatient
effective: 2023-06-01
performer: Organization/ExampleLab "Some lab"
value: Present (LOINC#LA9633-4)
component
code: Gene studied ID (LOINC#48018-6)
value: PABPN1 (HUGO Gene Nomenclature Committee Genes#HGNC:8565)
component
code: Cytogenetic (chromosome) location (LOINC#48001-2)
value: chr14 ()
component
code: Transcript reference sequence [ID] (LOINC#51958-7)
value: NM_004643.4 (Gene Reference Sequence Collection#NM_004643.4)
component
code: DNA change (c.HGVS) (LOINC#48004-6)
value: NM_004643.3:c.3GGC[14] (Human Genome Variation Society nomenclature#NM_004643.3:c.3GGC[14])
component
code: Genomic allele start-end (LOINC#81254-5)
value: 3-?
component
code: Discrete genetic variant (LOINC#81252-9)
value: NM_004643.3(PABPN1):c.3GGC[11] (p.Ala11_Gly12insAlaAlaAlaAla) (ClinVar Variant ID#503634)
component
Repeat Motif Order: 1
code: Repeat Expansion Motif (To Be Determined Codes#repeat-motif)
value: GGC
component
Repeat Motif Order: 1
code: Number of Repeat Expansions (To Be Determined Codes#repeat-number)
value: 11