Variant #0000665695 (NC_000005.9:g.[NC_000008.10:(159900000_168500000)_qter]delins(176563032_176618884)_qter)

Individual ID 00101356
Chromosome 5
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.[NC_000008.10:(159900000_168500000)_qter]delins(176563032_176618884)_qter
DNA change (hg38) -
Published as -
ISCN 46,XX,t(5;8)(q35;q24.1)
DB-ID chr5_000000 See all 4 reported entries
Variant remarks translocation
Reference -
ClinVar ID -
dbSNP ID -
Origin DUPLICATE record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-05-13 12:08:02 +02:00 (CEST)
Date last edited N/A




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000101804 DNA FISH - - NSD1 4 Johan den Dunnen


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