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
Back to search Result
Genomic Location

chr7:55181378

Clinvar Clinical Significance

Drug Response, Likely Pathogenic, Pathogenic

CTGA Clinical Significance

Drug Response, Likely Pathogenic, Pathogenic

Variant Type

Substitution

Clinvar

16613

Epidemiology in the Arab World

View Map
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...
© CAGS 2024. All rights reserved.