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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLA NM_000169.2 ./. 01 c.41T>C - p.Leu14Pro