Variant #0000000229 (NC_000017.10:g.40696008C>T, NM_000263.3:c.1984C>T (NAGLU))

Individual ID 00000020
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.40696008C>T
Reference -
DB-ID NAGLU_000002
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Variome.ir
Date created 2020-12-18 20:22:56 +00:00 (UTC)
Date last edited 2024-09-09 23:09:36 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Clinical classification     
NAGLU NM_000263.3 ./. - c.1984C>T r.(?) p.(Gln662*) pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000022 DNA SEQ-NG NAGLU 1 Variome.ir