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
Official URL: http://hl7.org/fhir/uv/genomics-reporting/ValueSet/molecular-consequence-vs | Version: 3.0.0-ballot | |||
Active as of 2023-12-18 | Computable Name: MolecularConsequenceVS |
The calculated or observed effect of a variant on its downstream transcript and, if applicable, ensuing protein sequence.
References
http://sequenceontology.org
where concept is-a SO:0001537
No Expansion for this valueset (Unknown Code System)
Explanation of the columns that may appear on this page:
Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
Code | The code (used as the code in the resource instance) |
Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
Definition | An explanation of the meaning of the concept |
Comments | Additional notes about how to use the code |