Variant #0000184421 (NC_000023.10:g.148564603G>A, NM_000202.5:c.1327C>T (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.148564603G>A
DNA change (hg38) g.149483072G>A
Published as -
ISCN -
DB-ID IDS_000011 See all 60 reported entries
Variant remarks expression cloning shows reduced activity, instable protein
Reference PubMed: Sukegawa 1992
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site TaqI-
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 2009-11-28 19:57:45 +01:00 (CET)
Date last edited 2024-10-08 19:48:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDS NM_000202.5 +/. 9 c.1327C>T - p.Arg443*


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