NM_000492.3:c.254G>A

HGVS Expressions

  • NG_016465.4:g.48340G>A
  • NM_000492.3:c.254G>A
  • NP_000483.3:p.Gly85Glu
  • NC_000007.14:g.117509123G>A
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Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

7143

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
219700.G.6.15Tunisia4PathogenicCystic FibrosisMessaoud et al. 2005 2 patients from unrelated families
219700.G.6.16Tunisia2PathogenicCystic FibrosisMessaoud et al. 2005 2 patients from unrelated families
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