EGFR gene c.2156G>C+2155G>A+2155G>T [Presence] in Blood or Tissue by Molecular genetics method 55765-2
LOINC Code
| LOINC code | 55765-2 | ||
|---|---|---|---|
| name | EGFR gene c.2156G>C+2155G>A+2155G>T [Presence] in Blood or Tissue by Molecular genetics method | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | EGFR gene.c.2156G>C+2155G>A+2155G>T | ||
| property | Arb = Arbitrary | ||
| time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
| system | Bld/Tiss Bld = Whole blood Tiss = Tissue, unspecified | ||
| scale | Ord = Ordinal: Ordered categorical responses, e.g., 1+, 2+, 3+; positive, negative; reactive, indeterminate, nonreactive. | ||
| method | Molgen = Molecular Genetics: General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods. | ||
Additional Names | |||
| short name | EGFR c.2156G>C+2155G>A+2155G>T Bld/T Ql | ||
Basic Attributes | |||
| class | MOLPATH.MUT | ||
| type | 1 Laboratory | ||
| order vs. observation | Both | ||
Associated Observations | |||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||
History/Usage | |||
| first released | |||
| last updated | 2.40 | ||
| last change type | MIN - change to field other than name | ||
| change reason | Changed Component part of 'p' to 'c' and variants to 2156G>C, 21155G>A, and 2155G>T since these variants are at the coding level (vs. protein level) and to model HGVS nomenclature guidelines. | ||
Related Names | |||
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