Variant #0000003999 (NC_000023.10:-, GLA(NM_000169.2):c.3G>A)

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID GLA_00019 See all 2 reported entries
Frequency -
Variant remarks S.S., who was found to have a G>A transition at nucleotide position 3 (Fi. 2A), that is, the G of the initiating methionine codon. This converts the initiation codon into an isoleucine codon (MlI) and should result in the failure of correct initiation of translation. The next ATG codon is an in-frame methionine codon at amino acid position 42, which is 11 amino acids after the signal peptide cleavage site, so it is unlikely that this mutation would result in any residual a-gal

activity.
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 ./. 01 c.3G>A - p.Met1Ile