Variant #0000561491 (NC_000017.10:g.40688504_40688527dup, NM_000263.3:c.214_237dup (NAGLU))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.40688504_40688527dup
DNA change (hg38) g.42536486_42536509dup
Published as NAGLU(NM_000263.3):c.214_237dupGCGGCGCGCGTGCGGGTGCGCGGC (p.A72_G79dup)
ISCN -
DB-ID NAGLU_000048 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAGLU NM_000263.3 +/. - c.214_237dup r.(?) p.(Ala72_Gly79dup)


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