42780-7

LOINC 2.82

CCND1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

CCND1 gene Mut Anl Bld/T

Component

  • CCND1 gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • B-cell CLL; BCL1; BCL-1; Blood; Cyclin D1; D11S287E; Genetics; Heredity; Heritable; HGNC:988; Identity or presence; Inherited; Lymphoma 1; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; Parathyroid adenomatosis 1; PCR; Point in time; PRAD1; Random; Tissue; Tissue, unspecified; U21B31; WB; Whole blood; Whole blood or Tissue

Index terms

  • B-cell CLL
  • BCL-1
  • BCL1
  • Blood
  • CCND1 gene targeted mutation analysis
  • Cyclin D1
  • D11S287E
  • Genetics
  • Heredity
  • Heritable
  • HGNC:988
  • Identity or presence
  • Inherited
  • Lymphoma 1
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Anl
  • Mutations
  • Nominal
  • Parathyroid adenomatosis 1
  • PCR
  • Point in time
  • PRAD1
  • Random
  • Tissue
  • Tissue, unspecified
  • U21B31
  • WB
  • Whole blood
  • Whole blood or Tissue