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NM_006457.5:c.*1061T>C
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NM_006457.5:c.*1061T>C
HGVS Expressions
NM_006457.5:c.*1061T>C
NP_006448.5:p.?
NC_000004.12:g.94665128T>C
Associated Genes
PDZ and LIM Domain Protein 5
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CTGA Clinical Significance
Benign
Variant Type
Substitution
dbSNP
10590
Epidemiology in the Arab World
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United Arab Emirates
Subject ID
Country of Origin
Allele Count
Allele Frequency
CTGA Clinical Significance
Condition(s)
Reference
Remarks
181500.G.1
United Arab Emirates
79
0.341
Benign
Moselhy et al. 2015
121 patients (71 males, 50 females) diag...
181500.G.2
United Arab Emirates
113
0.336
Benign
Moselhy et al. 2015
174 control subjects
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Contributors
Pratibha Nair: 29.06.2022
Edit History
Asha Deepthi: 05.12.2022
Pratibha Nair: 29.06.2022
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