NM_000388.3:c.2956G>T

  1. Home
  2. NM_000388.3:c.2956G>T

HGVS Expressions

  • NG_009058.1:g.106228G>T
  • NM_000388.3:c.2956G>T
  • NP_000379.2:p.Ala986Ser
  • NC_000003.12:g.122284910G>T

Associated Genes

Calcium-Sensing Receptor
Back to search Result
Clinvar Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1801725

Clinvar

8349

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
125853.G.40.4United Arab Emirates0.226Osman et al. 2018 328 patients with T2DM
Download Table

Contributors

  • Pratibha Nair: 01.06.2022

Edit History

  • Pratibha Nair: 11.01.2023
  • Pratibha Nair: 01.06.2022
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.