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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