69487-7
LaboratoryTNFRSF13B gene full mutation analysis in Blood or Tissue by Sequencing
Definition
Sequencing of the entire coding region (full gene sequencing) within the TNFRSF13B gene (also known as TACI gene) is performed to identify mutations or variants in individuals with clinical features such as common variable immunodeficiency (CVID), selective IgA deficiency, lymphoproliferative disease associated with CVID, and autoimmune phenotypes with CVID. The TNFRSF13B gene, located on chromosome 17, consists of 5 exons spanning approximately 35 kb.
LOINC 6-Axis Classification
Component
TNFRSF13B gene full mutation analysis
Property
Find
Time Aspect
Pt
System
Bld/Tiss
Scale Type
Doc
Method Type
Sequencing
Details
Class
MOLPATH.MUT
Order/Observation
Both
Short Name
TNFRSF13B gene Full Mut Anl Bld/T Seq
Display Name
TNFRSF13B gene full mutation analysis Sequencing Doc (Bld/Tiss)
Related Names
Frequently Asked Questions
What is LOINC code 69487-7?
LOINC code 69487-7 identifies "TNFRSF13B gene full mutation analysis in Blood or Tissue by Sequencing". Sequencing of the entire coding region (full gene sequencing) within the TNFRSF13B gene (also known as TACI gene) is performed to identify mutations or variants in individuals with clinical features such as common variable immunodeficiency (CVID), selective IgA deficiency, lymphoproliferative disease associated with CVID, and autoimmune phenotypes with CVID. The TNFRSF13B gene, located on chromosome 17, consists of 5 exons spanning approximately 35 kb.
What does 69487-7 measure?
This code measures TNFRSF13B gene full mutation analysis in Bld/Tiss. It belongs to the MOLPATH.MUT class in the LOINC classification.
What is LOINC?
LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.