Variant #0000667041 (NC_000002.11:g.pter_85474807delins[NC_000011.9:pter_16035758])

Individual ID 00302556
Chromosome 2
Allele Unknown
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.pter_85474807delins[NC_000011.9:pter_16035758]
DNA change (hg38) -
Published as -
ISCN 46,XY,t(2;11)(p11.2;p15.2)
DB-ID chr2_016758
Variant remarks -
Reference PubMed: Tolchin 2020
ClinVar ID -
dbSNP ID -
Origin De novo
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 2020-05-24 15:52:32 +02:00 (CEST)
Date last edited N/A




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000303677 DNA SEQ;SEQ-NG - WGS SOX6 4 Johan den Dunnen


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