Variant #0000831663 (NC_000022.10:g.(?_21714498)_(24953112_?)dup)

Individual ID 00398062
Chromosome 22
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_21714498)_(24953112_?)dup
DNA change (hg38) g.(?_21360209)_(24598823_?)dup
Published as hg18 18640301-21928915dup
ISCN -
DB-ID chr22_003024
Variant remarks 3.2 Mb interstitial duplication
Reference PubMed: Hilhorst-Hofstee 2013
ClinVar ID -
dbSNP ID -
Origin Germline
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 2021-12-31 11:08:47 +01:00 (CET)
Date last edited 2021-12-31 11:09:48 +01:00 (CET)
Options




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000399305 DNA arraySNP - - SMAD3 2 Johan den Dunnen


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.