Variant #0000561490 (NC_000017.10:g.40688460C>G, NM_000263.3:c.170C>G (NAGLU))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.40688460C>G
DNA change (hg38) g.42536442C>G
Published as NAGLU(NM_000263.3):c.170C>G (p.(Ala57Gly)), NAGLU(NM_000263.4):c.170C>G (p.A57G)
ISCN -
DB-ID NAGLU_000047 See all 3 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +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.170C>G r.(?) p.(Ala57Gly)


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