NM_002524.5:c.38G>A

HGVS Expressions

  • NG_007572.1:g.5772G>A
  • NM_002524.5:c.38G>A
  • NP_002515.1:p.Gly13Asp
  • NC_000001.11:g.114716123C>T
Back to search Result
Clinvar Clinical Significance

Likely Pathogenic, Pathogenic

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Clinvar

13901

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
188550.G.1LebanonLikely PathogenicThyroid Carcinoma, PapillaryFakhruddin et al. 2017 253 cases of PTC
© CAGS 2024. All rights reserved.