Variant #0000015057 (NC_000023.10:-, TAZ(NM_000116.3):c.159dup)

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Duplication
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID TAZ_00041
Frequency -
Variant remarks LVNC, like other forms of inherited cardiomyopathy, is a genetically

heterogeneous disease, associated with variable clinical symptoms and can be inherited as an autosomal or X-linked recessive disorder.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAZ NM_000116.3 ./. 02 c.159dup - p.Ile54HisfsX80