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 82536-4: SOS1 gene full mutation analysis Sequencing Doc (Bld/Tiss)

Name: LOINC Code 82536-4: SOS1 gene full mutation analysis Sequencing Doc (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T09:00:08.165Z

82536-4 is a LOINC code used to identify SOS1 gene full mutation analysis Sequencing Doc (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 SOS1 gene full 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 SOS1 gene full 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: Sequencing

What it does not mean

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

Key facts

SOS1 gene full mutation analysis in Blood or Tissue by Sequencing

SOS1 gene full mutation analysis

Full sequencing analysis of all 23 coding exons and intron/exon boundaries of the SOS1 gene is performed to aid in the diagnosis of SOS1-associated Noonan syndrome and hereditary gingival fibromatosis.[GHR geneSOS1]

Blood; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; GF1; GGF1; GINGF; Heredity; Heritable; HGF; high-throughput sequencing; HTS; Inherited; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; Next generation sequencing; NGS; NS4; Point in time; Random; sequencing of entire coding region; son of sevenless homolog 1 (Drosophila); SOS-1; Tissue; Tissue, unspecified; 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

SOS1 gene full mutation analysis Sequencing Doc (Bld/Tiss)SOS1 gene full mutation analysis in Blood or Tissue by SequencingSOS1 gene Full Mut Anl Bld/T SeqSOS1 gene full mutation analysisMOLPATH.MUTSOS1 gene variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code82536-4

SystemLOINC

Display nameSOS1 gene full mutation analysis Sequencing Doc (Bld/Tiss)

DescriptionSOS1 gene full mutation analysis

Short nameSOS1 gene Full Mut Anl Bld/T Seq

ComponentSOS1 gene full mutation analysis

PropertyFind

TimingPt

System (specimen)Bld/Tiss

ScaleDoc

MethodSequencing

ClassMOLPATH.MUT

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.58

Last changed2.65

Consumer names

SOS1 gene variant analysis, Blood or tissue specimen

Part names

SOS1 gene full mutation analysisFindPtBld/TissDocSequencingFindingPoint in time (spot)Blood or Tissue

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.