Variant #0000169460 (NC_000023.10:g.(pter_cen_qter)sup)

Individual ID 00103955
Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(pter_cen_qter)sup
DNA change (hg38) -
Published as 47,XXY
ISCN 47,XXY
DB-ID chrX_002751
Variant remarks -
Reference -
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 Le Gall
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-05-05 20:05:45 +02:00 (CEST)
Date last edited 2020-05-10 14:24:38 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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0000104414 DNA FISH - - ELN, LAT2 2 Le Gall


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