72520-0
FLT3 gene.p.Asp835+Ile836 mutations [Presence] in Blood or Tissue by Molecular genetics method
Active
Term Description
Point mutations and deletions of codons D835 and I836 within the second tyrosine kinase domain (protein activation loop) of the FLT3 gene are detected by molecular genetic methods (e.g. PCR-based assays). This code was created for, but not limited to Invivoscribe's LeukoStrat(tm) FLT3 Gel Detection Mutation Assay, which detects the presence or absence of either D835 or I836 mutations within the second TKD but does not identify specific TKD mutations. FLT3-TKD mutations occur in approximately 7% of patients with acute myelogenous leukemia (AML).
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- FLT3 gene.p.Asp835+Ile836 mutations
- Property
- PrThr
- Time
- Pt
- System
- Bld/Tiss
- Scale
- Ord
- Method
- Molgen
Additional Names
- Short Name
- FLT3 p.D835+I836 Bld/T Ql
- Display Name
- FLT3 gene.p.Asp835+Ile836 mutations Molgen Ql (Bld/Tiss)
- Consumer Name Alpha Get Info
- FLT3 gene.p.Asp835+Ile836 mutations, Blood or tissue specimen
Example Answer List: LL360-9
Source: Regenstrief InstituteAnswer | Code | Score | Answer ID |
---|---|---|---|
PositiveCopyright http://snomed.info/sct ID:10828004 Positive (qualifier value) | LA6576-8 | ||
NegativeCopyright http://snomed.info/sct ID:260385009 Negative (qualifier value) | LA6577-6 |
Basic Attributes
- Class
- MOLPATH.MUT
- Type
- Laboratory
- First Released
- Version 2.42
- Last Updated
- Version 2.73
- Change Reason
- Release 2.71: COMPONENT: Changed for nomenclature consistency.; Previous Releases: Changed Component name to align with the current HGVS recommendations to use the three letter codes for amnio acids. In the shortname, we kept the single letter codes.; The PrThr property is used for LOINC terms whose results are reported using an ordered categorical scale, regardless of whether or not an internal threshold was used to make that determination. This change was approved by the Laboratory LOINC Committee in June 2016.
- Order vs. Observation
- Both
- Common Test Rank Get Info
- 5547
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
de-AT | German (Austria) | Synonyms: FLT3 Genmutation (Asp835+Ile836) |
es-ES | Spanish (Spain) | Gen FLT3 pD835+I836: |
es-MX | Spanish (Mexico) | Gen FLT3 p. Asp835 + Ile836: |
fr-CA | French (Canada) | Gène FLT3.p.Asp835+Ile836, Mutations: |
fr-FR | French (France) | FLT3 gène p.Asp835+Ile836: |
it-IT | Italian (Italy) | FLT3, gene.p.Asp835+mutazioni Ile836: Synonyms: Gene FLT3 Gene FLT3 p.Asp835+mutazioni Ile836 Genetica molecolare Mutazione genica Patologia molecolare Presenza o Soglia Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
nl-NL | Dutch (Netherlands) | FLT3 gen.p.Asp835+Ile836 mutaties: Synonyms: FLT3 gen molgen |
pt-BR | Portuguese (Brazil) | FLT3 gene.p.D835+I836: |
ru-RU | Russian (Russian Federation) | FLT3 ген.p.D835+I836: Synonyms: Кровь Кровь или Ткань Порядковый Ткань и мазки Точка во времени; |
tr-TR | Turkish (Turkey) | FLT3 geni.p.D835+I836: Synonyms: Mevcut |
zh-CN | Chinese (China) | FLT3 基因.p.Asp835+Ile836 突变: Synonyms: FL 细胞因子受体前体; |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=72520-0
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LOINC Copyright
Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright