ARCHETYPE Genetic substitution variant (openEHR-EHR-CLUSTER.substitution_variant.v0)

ARCHETYPE IDopenEHR-EHR-CLUSTER.substitution_variant.v0
ConceptGenetic substitution variant
DescriptionA genetic sequence change where, compared to a reference sequence, one nucleotide is replaced by one other nucleotide.
UseUse to record the findings for a substitution variant observed in a genetic sequence according to the HGVS nomenclature. This archetype has been specifically designed to be used in the 'Variant' SLOT within the CLUSTER.genetic_variant archetype, but can also be used within other ENTRY or CLUSTER archetypes, where clinically appropriate.
PurposeTo record the details about a substitution variant observed in a genetic sequence according to the HGVS nomenclature.
Referencesden Dunnen JT, Dalgleish R, Maglott DR, Hart RK, Greenblatt MS, McGowan-Jordan J, Roux AF, Smith T, Antonarakis SE, Taschner PE. HGVS Recommendations for the Description of Sequence Variants: 2016 Update. Hum Mutat. 2016 Jun;37(6):564-9. doi: 10.1002/humu.22981. Epub 2016 Mar 25. PubMed PMID: 26931183.
Copyright© openEHR Foundation
AuthorsAuthor name: Cecilia Mascia
Organisation: CRS4, Italy
Email: cecilia.mascia@crs4.it
Date originally authored: 2017-02-23
Other Details LanguageAuthor name: Cecilia Mascia
Organisation: CRS4, Italy
Email: cecilia.mascia@crs4.it
Date originally authored: 2017-02-23
Other Details (Language Independent)
  • Licence: This work is licensed under the Creative Commons Attribution-ShareAlike 4.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by-sa/4.0/.
  • Custodian Organisation: Ocean Informatics
  • References: den Dunnen JT, Dalgleish R, Maglott DR, Hart RK, Greenblatt MS, McGowan-Jordan J, Roux AF, Smith T, Antonarakis SE, Taschner PE. HGVS Recommendations for the Description of Sequence Variants: 2016 Update. Hum Mutat. 2016 Jun;37(6):564-9. doi: 10.1002/humu.22981. Epub 2016 Mar 25. PubMed PMID: 26931183.
  • Original Namespace: com.oceaninformatics
  • Original Publisher: Ocean Informatics
  • Custodian Namespace: com.oceaninformatics
  • MD5-CAM-1.0.1: CDA5DB1A18B9E9082228C170FD51911D
  • Build Uid: c4a6ffce-a1d1-4e95-9fc4-bc3dc5593ecf
  • Revision: 0.0.1-alpha
Keywordssubstitution, variation, genetic, genomic, variant
Lifecyclein_development
UID2d2a0dd1-0729-4468-98bb-a5935f01a33f
Language useden
Citeable Identifier1013.1.2349
Revision Number0.0.1-alpha
items
Position substitutedPosition substituted: The position of the sustituted nucleotide.
Reference nucleotideReference nucleotide: The nucleotide at reference position.
New nucleotideNew nucleotide: Substituted nucleotide.
Reference sequenceReference sequence: The sequence file that has been used as a reference to describe the variant.
Include:
openEHR-EHR-CLUSTER.reference_sequence.v1 and specialisations
Other contributorsChristina Jaeger-Schmidt, Heidelberg University Hospital, Germany
Florian Kaercher, Charité Berlin, Germany
Francesca Frexia, CRS4, Italy
Gianluigi Zanetti, CRS4, Italy
Heather Leslie, Atomica Informatics, Australia (openEHR Editor)
Gideon Giacomelli, Charité Berlin, Germany
Paolo Uva, CRS4, Italy
Silje Ljosland Bakke, Nasjonal IKT HF, Norway (openEHR Editor)
Simon Schumacher, HiGHmed, Germany
Translators
  • German: Aurelie Tomczak, Institute of Pathology, University Hospital Heidelberg, Germany, au.tomczak@yahoo.com