What does this LOINC code represent?

This LOINC code identifies a lab observation, measurement, question, or clinical concept in a standardized format.

Is this enough to understand my test result?

No. The code identifies the test or observation, but the interpretation depends on the actual result, reference range, and clinical context.

LOINCActiveBoth

LOINC Code 35744-2: TP73L gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Name: LOINC Code 35744-2: TP73L gene targeted mutation analysis Molgen Nom (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T08:59:23.499Z

35744-2 is a LOINC code used to identify TP73L gene targeted mutation analysis Molgen Nom (Bld/Tiss) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component TP73L gene targeted mutation analysis. It is commonly used with the system or sample type Bld/Tiss.

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component TP73L gene targeted mutation analysis. It is commonly used with the system or sample type Bld/Tiss.

When is it used?

Used in lab systems, EHRs, and clinical data exchange.
May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
Status: ACTIVE
Order vs observation: Both
Method: Molgen

What it does not mean

The code identifies the observation or test, not the actual result.

Key facts

TP73L gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

TP73L gene targeted mutation analysis

AIS; B(p51A); B(p51B); Blood; Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome; EEC dysplasia; EEC3; Genetics; Heredity; Heritable; HGNC15979; Identity or presence; Inherited; KET; LMS; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; NBP; Nominal; OFC8; p40; p51; p53CP; p63; p73H; p73L; PCR; Point in time; Random; RHS; SHFM4; Tissue; Tissue, unspecified; TP53CP; TP53L; TP63; TP73L; Tumor protein 63 kDa with strong homology to p53 gene; tumor protein p63; Tumor protein p73-like gene; WB; Whole blood; Whole blood or Tissue

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

TP73L gene targeted mutation analysis Molgen Nom (Bld/Tiss)TP73L gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method NominalTP73L gene Mut Anl Bld/TTP73L gene targeted mutation analysisMOLPATH.MUTTP73L gene targeted mutation analysis, Blood or tissue specimenPrid

Frequently asked questions

Code details

Code35744-2

SystemLOINC

Display nameTP73L gene targeted mutation analysis Molgen Nom (Bld/Tiss)

DescriptionTP73L gene targeted mutation analysis

Short nameTP73L gene Mut Anl Bld/T

ComponentTP73L gene targeted mutation analysis

PropertyPrid

TimingPt

System (specimen)Bld/Tiss

ScaleNom

MethodMolgen

ClassMOLPATH.MUT

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.13

Last changed2.68

Consumer names

TP73L gene targeted mutation analysis, Blood or tissue specimen

Part names

TP73L gene targeted mutation analysisPridPtBld/TissNomMolgenPresence or IdentityPoint in time (spot)Blood or TissueMolecular genetics

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.