Variant #0000015004 (NC_000023.10:-, TAZ(NM_000116.3):c.110-2A>G)

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_00054
Frequency -
Variant remarks The characterization of mutations of the

G4.5 gene will be useful for carrier detection, genetic

counseling, and the identification of patients with Barth

syndrome who do not manifest all of the cardinal

features of this disorder.

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 ./. 02 c.110-2A>G - -