NM_005228.5:c.2369C>T

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  2. NM_005228.5:c.2369C>T

HGVS Expressions

  • NG_007726.3:g.167347C>T
  • NM_005228.5:c.2369C>T
  • NP_005219.2:p.Thr790Met

Associated Genes

Epidermal Growth Factor Receptor
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Genomic Location

chr7:55181378

Clinvar Clinical Significance

Drug Response, Likely Pathogenic, Pathogenic

CTGA Clinical Significance

Drug Response, Likely Pathogenic, Pathogenic

Variant Type

Substitution

dbSNP

121434569

Clinvar

16613

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
211980.4LebanonDrug Response, Likely Pathogenic, PathogenicLung CancerNaderi et al, 2015 EGFR mutation observed in one patient fr...
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Contributors

  • Asha Deepthi: 01.07.2020

Edit History

  • Asha Deepthi: 02.07.2020
  • Asha Deepthi: 01.07.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.