NM_000492.4:c.869+11C>T

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HGVS Expressions

  • NG_016465.4:g.75901C>T
  • NM_000492.4:c.869+11C>T
  • NC_000007.14:g.117536684C>T

Associated Genes

Cystic Fibrosis Transmembrane Conductance Regulator
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

1800503

Clinvar

93159

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
219700.G.12Lebanon12NAUncertain SignificanceCystic FibrosisFarhat et al, 2015 Patients from 7 Lebanese families. c.390...
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Contributors

  • Asha Deepthi: 01.11.2020

Edit History

  • Asha Deepthi: 21.03.2021
  • Asha Deepthi: 17.03.2021
  • Asha Deepthi: 01.11.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.