Variant #0001018235 (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 ACMG
Clinical classification pathogenic (recessive)
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 Three patients are siblings (Parkinson et al,.,2004) and two are female (Dvorakova et al., 2017; Sukegawa et al., 1997). In one patient the variant is described in cis with c.1394A>T (Amartino et al., 2014) and is reported in HGMD 2022.3 as a unique delins (CX149681)
Reference PubMed: Zanetti 2024
ClinVar ID SCV000929887.1
dbSNP ID rs113993946
Origin SUMMARY record
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 2024-12-06 15:50:52 +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 +/. 9 c.1403G>A r.(?) p.(Arg468Gln)


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