NM_000660.4:c.29C>T

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HGVS Expressions

  • NG_013364.1:g.5911C>T
  • NM_000660.4:c.29C>T
  • NP_000651.3:p.Pro10Leu
  • NC_000019.10:g.41353016G>A

Associated Genes

Transforming Growth Factor, Beta-1
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1800470

Clinvar

12534

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.601BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
145500.G.10.1United Arab Emirates710.51BenignFrossard et al. 2002 70 hypertensives
145500.G.10.2United Arab Emirates780.54BenignFrossard et al. 2002 72 normotensives
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Contributors

  • Pratibha Nair: 05.09.2021
  • Sami Bizzari: 29.03.2021

Edit History

  • Sayeeda Hana: 13.01.2023
  • Pratibha Nair: 05.09.2021
  • Sami Bizzari: 29.03.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.