ERBB2 NM_004448.3:c.929C>A

MedGen UID:: 1780846
•Concept ID:: C5445401
•: Cell or Molecular Dysfunction

Synonyms:

ERBB2 c.929C>A; HER-2 c.929C>A; HER-2/neu c.929C>A; HER2 c.929C>A; NEU c.929C>A; NM_004448.3:c.929C>A; v-erb-b2 Erythroblastic Leukemia Viral Oncogene Homolog 2, Neuro/Glioblastoma Derived Oncogene Homolog (Avian) c.929C>A

Definition

A nucleotide substitution at position 929 of the coding sequence of the ERBB2 gene where cytosine has been mutated to adenine. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVERBB2 NM_004448.3:c.929C>A

Molecular Genetic Variation
- Gene Abnormality
  - Receptor Tyrosine Kinase Gene Mutation
    - ERBB2 Gene Mutation
      - Activating ERBB2 Mutation
        Activating ERBB2 Point Mutation
        ERBB2 NM_004448.3:c.929C>A

Supplemental Content

Practice guidelines

Bookshelf
See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

Recent activity

Clear Turn Off Turn On

ERBB2 NM_004448.3:c.929C>A
ERBB2 NM_004448.3:c.929C>A

MedGen
ERBB2 NM_004448.3:c.2033G>A
ERBB2 NM_004448.3:c.2033G>A

MedGen
Urea Cycle Disorders, Inborn
Urea Cycle Disorders, Inborn
Rare congenital metabolism disorders of the urea cycle. The disorders are due to mutations that result in complete (neonatal onset) or partial (childhood or adult onset) inact...<br/>Year introduced: 2010

MeSH

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

MedGen

National Center for Biotechnology Information