Variant #0001012662 (NC_000023.10:g.148564527C>T, NM_000202.5:c.1403G>A (IDS))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.148564527C>T
DNA change (hg38) g.149482996C>T
Published as -
ISCN -
DB-ID IDS_000014 See all 93 reported entries
Variant remarks in vitro cDNA expression COS7 cells no detectable enzyme activity
Reference PubMed: Lin 2019
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-10-27 14:25:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDS NM_000202.5 +/. - c.1403G>A - p.(Arg468Gln)


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