Variant #0000004541 (NC_000023.10:-, GLA(NM_000169.2):c.214A>G)

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type A to G transversion in exon 02
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID GLA_00440 See all 2 reported entries
Frequency -
Variant remarks This raises the possibility that the degree of

their intracellular stabilities reflects their own residual

enzyme activities in cells and phenotypic expression

of this disease.
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     
GLA NM_000169.2 ./. 02 c.214A>G - p.Met72Val