NM_000492.3:c.382T>C

HGVS Expressions

  • NG_016465.4:g.70224T>C
  • NM_000492.3:c.382T>C
  • NP_000483.3:p.Cys128Arg
  • NC_000007.14:g.117531007T>C
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
219700.G.2.7KuwaitNANAUncertain SignificanceCystic FibrosisSamilchuk, 2005 Unknown number of patients
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