NM_000492.3:c.3310G>T

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HGVS Expressions

  • NG_016465.4:g.150968G>T
  • NM_000492.3:c.3310G>T
  • NP_000483.3:p.Glu1104Ter
  • NC_000007.14:g.117611751G>T

Associated Genes

Cystic Fibrosis Transmembrane Conductance Regulator
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Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

dbSNP

397508538

Clinvar

53715

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
219700.G.6.13Tunisia4NAPathogenicCystic FibrosisMessaoud et al. 2005 2 patients from unrelated families
219700.G.6.14Tunisia5NAPathogenicCystic FibrosisMessaoud et al. 2005 5 patients from unrelated families
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Contributors

    Edit History

    • Asha Deepthi: 21.03.2021
    • Asha Deepthi: 30.04.2020
    • Asha Deepthi: 29.04.2020
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    © CAGS 2024. All rights reserved.