NM_033360.4:c.34G>A

HGVS Expressions

  • NG_007524.1:g.10570G>A
  • NM_033360.4:c.34G>A
  • NP_203524.1:p.Gly12Ser
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Genomic Location

chr12:25245351

Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

12584

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
211980.2LebanonPathogenicLung CancerFakhruddin et al, 2014 One patient from a study that included 1...
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