NM_000583.4:c.1296T>G

  1. Home
  2. NM_000583.4:c.1296T>G

HGVS Expressions

  • NG_012837.3:g.57904T>G
  • NM_000583.4:c.1296T>G
  • NP_000574.2:p.Asp432Glu
  • NC_000004.12:g.71752617A>C

Associated Genes

Group-Specific Component
Back to search Result
Clinical Significance

Benign

Variant Type

Substitution

dbSNP

7041

Clinvar

15987

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountClinical SignificanceCondition(s)ReferenceRemarks
139200.G.1LebanonAssociation,Uncertain SignificanceMedlej-Hashim et al. 2015 Study subjects with GG genotype of rs704...
Download Table

Contributors

  • Asha Deepthi: 22.02.2021

Edit History

  • Asha Deepthi: 22.02.2021
Back to search Result
© CAGS 2021. All rights reserved.
© CAGS 2021. All rights reserved.