Variant #0000234999 (NC_000004.11:g.(107700001_114100000)_qterdelins[NC_000008.10:(118811950_119123286)_qter])

Individual ID 00133224
Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(107700001_114100000)_qterdelins[NC_000008.10:(118811950_119123286)_qter]
DNA change (hg38) -
Published as -
ISCN t(4;8)(q25;q24.1)
DB-ID chr4_000576
Variant remarks -
Reference PubMed: Jennes, 2008
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Ivy Jennes
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-12-01 19:40:26 +01:00 (CET)
Date last edited 2020-05-12 19:21:26 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000134059 DNA FISH Blood - EXT1 4 Ivy Jennes


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