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NM_000256.3:c.776delinsTT
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NM_000256.3:c.776delinsTT
HGVS Expressions
NG_007667.1:g.9801delinsTT
NM_000256.3:c.776delinsTT
NP_000247.2:p.Ala259ValfsTer27
NC_000011.10:g.47347902delinsAA
Associated Genes
Myosin-Binding Protein C, Cardiac
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CTGA Clinical Significance
Likely Pathogenic
Variant Type
Indel
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
615396.1
United Arab Emirates
1
Likely Pathogenic
Left Ventricular Noncompaction 10
Al-Shamsi et al. 2016
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Contributors
Pratibha Nair: 20.07.2020
Edit History
Pratibha Nair: 03.01.2023
Pratibha Nair: 29.11.2022
Pratibha Nair: 23.08.2022
Rahila Mir: 17.02.2022
Pratibha Nair: 20.07.2020
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