81253-7

LOINC Code


LOINC code81253-7
name
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 nameFinding; Findings; Molecular pathology; MOLPATH; Nominal; Point in time; Random; Simp var name

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationSimple var name

History/Usage

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

Related Names



Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, 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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