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_018136.5:c.7782_7783del
Home
NM_018136.5:c.7782_7783del
HGVS Expressions
NG_015867.1:g.50226_50227del
NM_018136.5:c.7782_7783del
NP_060606.3:p.Lys2595SerfsTer6
NC_000001.11:g.197101469_197101470del
Associated Genes
Abnormal Spindle-Like, Microcephaly-Associated
Back to search Result
Clinvar Clinical Significance
Pathogenic
CTGA Clinical Significance
Likely Pathogenic, Pathogenic
Variant Type
Deletion
dbSNP
199422173
Clinvar
21606
Epidemiology in the Arab World
View Map
All Countries
Algeria
United Arab Emirates
Subject ID
Country of Origin
Allele Count
Allele Frequency
CTGA Clinical Significance
Condition(s)
Reference
Remarks
608716.3.1
Algeria
2
Likely Pathogenic
Microcephaly 5, Primary, Autosomal Recessive
Passemard et al. 2009
Proband
608716.3.2
Algeria
2
Likely Pathogenic
Microcephaly 5, Primary, Autosomal Recessive
Passemard et al. 2009
Sibling of 608716.3.1
608716.7
United Arab Emirates
2
Pathogenic
Microcephaly 5, Primary, Autosomal Recessive
Saleh et al. 2021
Sibling with learning difficulty
Download Table
Contributors
Pratibha Nair: 08.07.2021
Edit History
Sayeeda Hana: 07.12.2022
Pratibha Nair: 10.10.2021
Pratibha Nair: 11.07.2021
Pratibha Nair: 08.07.2021
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.