LOINC Code 35291-4: UBE3A gene targeted mutation analysis Molgen Nom (Bld)

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 UBE3A gene targeted mutation analysis. It is commonly used with the system or sample type Bld.

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

• UBE3A gene mutations found [Identifier] in Blood by Molecular genetics method Nominal
• UBE3A gene targeted mutation analysis
• ANCR; Angelman syndrome; AS; Blood; CTCL tumor antigen se37-2; E6AP; E6-AP; EPVE6AP; Genetics; Heredity; Heritable; HPVE6A; human papilloma virus E6-associated protein; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; oncogenic protein-associated protein E6-AP; PCR; Point in time; Random; ubiquitin protein ligase E3A; Ubiquitin-protein ligase E3A; WB; Whole blood

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

Frequently asked questions