Variant #0000004003 (NC_000023.10:-, GLA(NM_000169.2):c.41T>C)
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
L14P |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
GLA_00024 See all 2 reported entries |
Frequency |
- |
Variant remarks |
Direct DNA sequencing showed single T-to-C transi-
tion in codon 14 of exon 1. This was a missense mutation predicting a leucine to proline substitution (L14P). |
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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