NM_002187.2:c.*159A>C

  1. Home
  2. NM_002187.2:c.*159A>C

HGVS Expressions

  • NG_009618.1:g.19532A>C
  • NM_002187.2:c.*159A>C
  • NP_002178.2:p.?
  • NC_000005.10:g.159315942T>G

Associated Genes

Interleukin 12A
Back to search Result
Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

3212227

Clinvar

352569

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
Lebanese CytokineLebanon0.25BenignMahfouz et al. 2009 Frequency of cytokine gene alleles in 10...
Download Table

Contributors

  • Sami Bizzari: 29.03.2021

Edit History

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