Variant #0000015037 (NC_000023.10:-, TAZ(NM_000116.3):c.280C>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_00037
Frequency -
Variant remarks another patient with a missense mutation at the same position (R94C) has been previously reported

(Johnston et al. 1997). These data suggest that R94S is not

a common polymorphism, but a disease-causing mutation.
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 ./. 03 c.280C>A - p.Arg94Ser