COSMIC simple variant:ID:Pt: Patient:Nom:

Preferred Label : COSMIC simple variant:ID:Pt: Patient:Nom:;

LOINC status : TRIAL;

LOINC display name : COSMIC simple variant Nom [ID];

LOINC long common name : COSMIC [ID];

LOINC short name : COSMIC simple var ID;

LOINC description : The COSMIC ID is used to report the variant ID for the COSMIC database, which collects information about somatic cancer-related, non-structural mutations. Information in the COSMIC database includes an ID for the tissue source of the submission, a gene name, a reference sequence from Ensembl, pathogenicity, and HGVS names. For example, the COSMIC Mutation ID COSM34090 is for a missense mutation in the IDH2 gene with HGVS nomenclature c.516G T and p.R172S. [http://cancer.sanger.ac.uk/cosmic/mutation/overview?id 34090];

Details

Origin ID

81256-0;

UMLS CUI

C4265556;

Has component
- COSMIC [LOINC component]
- COSMIC simple variant [LOINC component]
- Simple variant [LOINC component]
Has property
- Identifier [LOINC Property]
Has scale
- Nom [LOINC scale]
Has system
- Patient [LOINC System]
- ^Patient [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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