Variant #0001018230 (NC_000023.10:g.148564536T>A, NM_000202.5:c.1394A>T (IDS))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.148564536T>A
DNA change (hg38) g.149483005T>A
Published as -
ISCN -
DB-ID IDS_000187 See all 2 reported entries
Variant remarks Reported in cis with c.1403G>A and reported in HGMD 2022.3 as a unique delins (CX149681)
Reference PubMed: Zanetti 2024
ClinVar ID SCV005089545
dbSNP ID rs113993951
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.1394A>T r.(?) p.(Gln465Leu)


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