NM_022168.3:c.1764del

  1. Home
  2. NM_022168.3:c.1764del

HGVS Expressions

  • NG_011495.1:g.45324del
  • NM_022168.3:c.1764del
  • NP_071451.2:p.Ala589LeufsTer16
  • NC_000002.12:g.162278213del

Associated Genes

Interferon-Induced Helicase C Domain-Containing Protein 1
Back to search Result
Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Deletion

dbSNP

553669430

Clinvar

987915

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
606951.1United Arab Emirates1Uncertain SignificanceIFIH1-Associated Viral Respiratory InfectionFathalla et al. 2021
Download Table

Contributors

  • Sami Bizzari: 27.01.2022

Edit History

  • Pratibha Nair: 12.09.2022
  • Sami Bizzari: 01.02.2022
  • Sami Bizzari: 27.01.2022
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.