Variant #0000000222 (NC_000023.10:g.148564365A>G, NM_000202.5:c.1565T>C (IDS))

Individual ID 00000016
Chromosome X
Allele Maternal (inferred)
Affects function (as reported) Not classified
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.148564365A>G
Reference -
DB-ID IDS_000002
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Variome.ir
Date created 2020-12-17 21:13:24 +00:00 (UTC)
Date last edited 2020-12-31 05:48:04 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Clinical classification     
IDS NM_000202.5 ./+ - c.1565T>C r.(?) p.(Leu522Pro) likely pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000018 DNA SEQ-NG IDS 1 Variome.ir