NM_000660.4:c.74G>C

  1. Home
  2. NM_000660.4:c.74G>C

HGVS Expressions

  • NG_013364.1:g.5956G>C
  • NM_000660.4:c.74G>C
  • NP_000651.3:p.Arg25Pro
  • NC_000019.10:g.41352971C>G

Associated Genes

Transforming Growth Factor, Beta-1
Back to search Result
Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1800471

Clinvar

38902

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.1845BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
145500.G.10.1United Arab Emirates110.08BenignFrossard et al. 2002 70 hypertensives
145500.G.10.2United Arab Emirates100.07BenignFrossard et al. 2002 72 normotensives
Download Table

Contributors

  • Pratibha Nair: 05.09.2021
  • Sami Bizzari: 29.03.2021

Edit History

  • Pratibha Nair: 05.09.2021
  • Sami Bizzari: 29.03.2021
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.