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LOINC Code 82535-6: KRAS gene full mutation analysis Sequencing Doc (Bld/Tiss)

82535-6 is a LOINC code used to identify KRAS 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 KRAS 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 KRAS 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

KRAS gene full mutation analysis in Blood or Tissue by Sequencing
KRAS gene full mutation analysis
Full sequencing analysis of all coding exons and intron/exon boundaries of the KRAS gene is performed to establish a diagnosis of KRAS-associated Noonan syndrome, cardiofaciocutaneous syndrome, Costello syndrome, and clinically related disorders.[OMIM190070][GHR gene: KRAS]
Blood; CFC2; C-K-RAS; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; KI-RAS; Kirsten ras 1; Kirsten rat sarcoma viral oncogene homolog; Kirsten rat sarcoma virus 2; KRAS1; KRAS1P; KRAS2; K-RAS2A; K-RAS2B; K-RAS4A; K-RAS4B; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; Next generation sequencing; NGS; NS; NS3; Oncogene KRAS1; Oncogene KRAS2; Point in time; Random; RASK1; RASK2; sequencing of entire coding region; Tissue; Tissue, unspecified; V-KI-RAS1 pseudogene; v-Ki-ras2 Kirsten rat sarcoma 2 viral oncogene homolog; 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

KRAS gene full mutation analysis Sequencing Doc (Bld/Tiss)KRAS gene full mutation analysis in Blood or Tissue by SequencingKRAS gene Full Mut Anl Bld/T SeqKRAS gene full mutation analysisMOLPATH.MUTKRAS gene variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code82535-6
SystemLOINC
Display nameKRAS gene full mutation analysis Sequencing Doc (Bld/Tiss)
DescriptionKRAS gene full mutation analysis
Short nameKRAS gene Full Mut Anl Bld/T Seq
ComponentKRAS 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

KRAS gene variant analysis, Blood or tissue specimen

Part names

KRAS 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.

LOINC Code 82535-6 | HealthAssure