NM_000586.3:c.114G>T

  1. Home
  2. NM_000586.3:c.114G>T

HGVS Expressions

  • NG_016779.1:g.5169G>T
  • NP_000577.2:p.Leu38=
  • NC_000004.12:g.122456327C>A

Associated Genes

Interleukin 2
Back to search Result
CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

2069763

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.3168BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
Download Table

Contributors

  • Pratibha Nair: 29.03.2021

Edit History

  • Pratibha Nair: 30.03.2021
  • Pratibha Nair: 29.03.2021
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.