NM_033360.4:c.37G>T

HGVS Expressions

  • NG_007524.1:g.10573G>T
  • NM_033360.4:c.37G>T
  • NP_203524.1:p.Gly13Cys
Back to search Result
Genomic Location

chr12:25245348

Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

45123

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
211980.G.4.5LebanonPathogenicLung CancerFakhruddin et al, 2014 Two patients from a study that included ...
© CAGS 2024. All rights reserved.