NM_006457.5:c.1141A>G

  1. Home
  2. NM_006457.5:c.1141A>G

HGVS Expressions

  • NM_006457.5:c.1141A>G
  • NP_006448.5:p.Thr381Ala
  • NC_000004.12:g.94640308A>G

Associated Genes

PDZ and LIM Domain Protein 5
Back to search Result
CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

7690296

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
181500.G.1United Arab Emirates1150.487BenignMoselhy et al. 2015 121 patients (71 males, 50 females) diag...
181500.G.2United Arab Emirates1690.488BenignMoselhy et al. 2015 174 control subjects
Download Table

Contributors

  • Pratibha Nair: 29.06.2022

Edit History

  • Pratibha Nair: 29.06.2022
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.