Variant #0000222798 (NC_000023.10:g.148606691_148608805ins[148569718_148585611])

Individual ID 00114374
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.148606691_148608805ins[148569718_148585611]
DNA change (hg38) -
Published as KT724868:g.261_2375
ISCN -
DB-ID chrX_002904
Variant remarks copy inserted in IDS gene
Variant Error [ESYNTAX]: This genomic variant has an error (char 37: Syntax error). Please fix this entry and then remove this message.
Reference PubMed: Alcántara-Ortigoza 2016
ClinVar ID -
dbSNP ID -
Origin DUPLICATE 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 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-11-03 16:38:15 +01:00 (CET)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000114831 DNA PCR;SEQ - - IDS 2 Miguel Angel Alcántara-Ortigoza


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