NM_033360.4:c.35G>C

HGVS Expressions

  • NG_007524.1:g.10571G>C
  • NM_033360.4:c.35G>C
  • NP_203524.1:p.Gly12Ala
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Genomic Location

chr12:25245350

Clinvar Clinical Significance

Likely Pathogenic, Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

45122

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
211980.G.4.2LebanonPathogenicLung CancerFakhruddin et al, 2014 11 patients from a study that included 1...
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