Simple variant name Nominal   81253-7

LOINC Code


LOINC code81253-7
nameSimple variant name Nominal
descriptionThis term is used to report the formal name of a simple variant, including the reference sequence and nucleotide change. For example, NM_014049.4(ACAD9):c.1249C>T (p.Arg417Cys) represents an ACAD9 gene variant with nucleotide change c.1249C>T and protein change p.Arg417Cys that has the NCBI reference sequence NM_014049.4. [http://www.ncbi.nlm.nih.gov/clinvar/variation/30880/]
statusTRIAL

Fully-Specified Name

componentSimple variant name
propertyFind  =  Finding
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
system^Patient
scaleNom  =  Nominal:  Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody.
method

Additional Names

short nameSimple var name

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationObservation

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

History/Usage

first released
last updated2.56
last change typeMIN  - change to field other than name

Related Names

Finding
Findings
Molecular pathology
MOLPATH
Nominal
Point in time
Random
Simp var name

Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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