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 |

Variant on transcripts
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