NM_003761.4:c.*143T>C

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  2. NM_003761.4:c.*143T>C

HGVS Expressions

  • NG_022887.1:g.9369T>C
  • NM_003761.4:c.*143T>C
  • NP_003752.2:p.?
  • NC_000002.12:g.85581859T>C

Associated Genes

Vesicle-Associated Membrane Protein 8
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

1010

Clinvar

1182311

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608320.G.2.3United Arab EmiratesNAAssociationCoronary Artery Disease, Autosomal Dominant, 1Osman et al. 2020 Study with 914 individuals. 22 SNPs show...
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Contributors

  • Asha Deepthi: 13.09.2021

Edit History

  • Pratibha Nair: 21.11.2022
  • Rahila Mir: 03.02.2022
  • Asha Deepthi: 11.10.2021
  • Asha Deepthi: 29.09.2021
  • Asha Deepthi: 13.09.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.