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EGFR NM_005228.3:c.2156delG

MedGen UID:
475855
Concept ID:
C3274222
Cell or Molecular Dysfunction
Synonyms: EGFR c.2156delG; EGFR NM_005228.3:c.2156del; Epidermal Growth Factor Receptor Gene c.2156delG; ERBB c.2156delG; ERBB1 c.2156delG; HER1 c.2156delG; NM_005228.3:c.2156del; NM_005228.3:c.2156delG

Definition

A deletion of a guanine at position 2156 from the coding sequence of the EGFR gene. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVEGFR NM_005228.3:c.2156delG

Recent clinical studies

Diagnosis

Mohar B, Smojver Ježek S, Rajković Molek K, Štemberger C, Kurpis M, Kupanovac Ž, Samaržija M, Jonjić N, Grahovac B
Cytopathology 2016 Dec;27(6):444-451. Epub 2016 Mar 18 doi: 10.1111/cyt.12325. PMID: 26990359

Prognosis

Mohar B, Smojver Ježek S, Rajković Molek K, Štemberger C, Kurpis M, Kupanovac Ž, Samaržija M, Jonjić N, Grahovac B
Cytopathology 2016 Dec;27(6):444-451. Epub 2016 Mar 18 doi: 10.1111/cyt.12325. PMID: 26990359

Clinical prediction guides

Mohar B, Smojver Ježek S, Rajković Molek K, Štemberger C, Kurpis M, Kupanovac Ž, Samaržija M, Jonjić N, Grahovac B
Cytopathology 2016 Dec;27(6):444-451. Epub 2016 Mar 18 doi: 10.1111/cyt.12325. PMID: 26990359

Supplemental Content

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