العربية
About Us
News
Fellowships
العربية
Home
About Us
CTGA Database
CTGA Overview
Search Database
Submit to Database
Publications
Research Articles
Genetics Made Easy
Genetic Disorders in the Arab World
Reports
Conferences & Events
News
Gallery
Fellowships
Contact Us
NM_032856.3:c.129T>G
Home
NM_032856.3:c.129T>G
HGVS Expressions
NG_042034.1:g.6561T>G
NM_032856.3:c.129T>G
NP_116245.2:p.Tyr43Ter
Associated Genes
WD Repeat-Containing Protein 73
Back to search Result
Genomic Location
chr15: 84652783
Clinvar Clinical Significance
Pathogenic
CTGA Clinical Significance
Pathogenic
Variant Type
Substitution
dbSNP
727502863
Clinvar
162610
Epidemiology in the Arab World
View Map
Morocco
Subject ID
Country of Origin
Allele Count
Allele Frequency
CTGA Clinical Significance
Condition(s)
Reference
Remarks
251300.3.1
Morocco
2
Pathogenic
Galloway-Mowat Syndrome 1
Colin et al, 2014
251300.3.2
Morocco
2
Pathogenic
Galloway-Mowat Syndrome 1
Colin et al, 2014
Sibling of 251300.3.1
251300.3.3
Morocco
1
Pathogenic
Colin et al, 2014
Father of 251300.3.1
251300.3.4
Morocco
1
Pathogenic
Colin et al, 2014
Mother of 251300.3.1
Download Table
Contributors
Sami Bizzari: 28.07.2019
Edit History
Sami Bizzari: 07.05.2020
Sami Bizzari: 28.07.2019
Back to search Result
×
Algeria
Bahrain
Comoros
Country not specified
Djibouti
Egypt
Eritrea
Iraq
Jordan
Kuwait
Lebanon
Libya
Mauritania
Morocco
Oman
Palestine
Qatar
Saudi Arabia
Somalia
Sudan
Syria
Tunisia
United Arab Emirates
Yemen
Arab Countries with reported incidence
Arab Countries without reported incidence
Non-Arab Countries
© CAGS 2024. All rights reserved.