NM_000492.3:c.3964-28G>A

HGVS Expressions

  • NG_016465.4:g.203877G>A
  • NM_000492.3:c.3964-28G>A
  • NC_000007.14:g.117664660G>A
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

53863

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
219700.9Lebanon1NAUncertain SignificanceCystic FibrosisDesgeorges et al. 1997 Compound heterozygous patient from famil...
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