Variant #0000832395 (NC_000023.10:g.(?_52982784)_(53712951_?)dup, NM_001111125.1:c.-201_*1336{2} (IQSEC2))

Chromosome X
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_52982784)_(53712951_?)dup
DNA change (hg38) -
Published as hg19 52982784_53712951dup
ISCN -
DB-ID HUWE1_000176 See all 2 reported entries
Variant remarks 730kb duplication affecting TSPYL2, KDM5C, IQSEC2, SMC1A, HUWE1
Reference PubMed: Froyen 2012
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
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 2022-01-06 09:27:03 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IQSEC2 NM_001111125.1 +/. _1_15_ c.-201_*1336{2} r.? p.?


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.