Variant #0000015044 (NC_000023.10:-, TAZ(NM_000116.3):c.532T>A)

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID TAZ_00022 See all 2 reported entries
Frequency -
Variant remarks We suggest that males presenting

with cardiomyopathy, particularly during infancy, even in the absence of the typical signs of Barth syndrome, should be

evaluated for mutations in G4.5.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAZ NM_000116.3 ./. 06 c.532T>A - p.Phe178Ile