Variant #0000000268 (NC_000017.10:g.40695718G>A, NAGLU(NM_000263.3):c.1694G>A)

Individual ID 00000056
Chromosome 17
Allele Both (homozygous)
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.40695718G>A
Reference -
DB-ID NAGLU_000003
Average frequency (gnomAD v.2.1.1) 5.0E-5 View details
Owner Variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Variome.ir
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Clinical classification     
NAGLU NM_000263.3 ./. - c.1694G>A r.(?) p.(Arg565Gln) pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000059 DNA SEQ-NG NAGLU 1 Variome.ir