NM_033360.4:c.35G>A

HGVS Expressions

  • NG_007524.1:g.10571G>A
  • NM_033360.4:c.35G>A
  • NP_203524.1:p.Gly12Asp
Back to search Result
Genomic Location

chr12:25245350

Clinvar Clinical Significance

Likely Pathogenic, Pathogenic

CTGA Clinical Significance

Likely Pathogenic, Pathogenic

Variant Type

Substitution

Clinvar

12582

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
211980.G.4.3LebanonLikely Pathogenic, PathogenicLung CancerFakhruddin et al, 2014 Five patients from a study that included...
© CAGS 2024. All rights reserved.