NM_024876.4:c.1199dup

  1. Home
  2. NM_024876.4:c.1199dup

HGVS Expressions

  • NG_027800.1:g.25887dup
  • NM_024876.4:c.1199dup
  • NP_079152.3:p.His400GlnfsTer11
  • NC_000019.10:g.40695999dup

Associated Genes

Coenzyme Q8B
Back to search Result
Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Duplication

dbSNP

398122982

Clinvar

91850

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615573.6Arab2PathogenicNephrotic Syndrome, Type 9Korkmaz et al, 2016
Download Table

Contributors

  • Sayeeda Hana: 15.04.2020

Edit History

  • Pratibha Nair: 22.11.2022
  • Sayeeda Hana: 09.03.2021
  • Sayeeda Hana: 17.04.2020
  • Sayeeda Hana: 15.04.2020
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.