Variant #0000061653 (NC_000021.8:g.(21633033_22115159)_(23685731_24622562)del)

Individual ID 00034491
Chromosome 21
Allele Paternal (confirmed)
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.(21633033_22115159)_(23685731_24622562)del
DNA change (hg38) -
Published as g.(21633033_22115159)_(23685731_24622562)del
ISCN -
DB-ID chr21_000117
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation no
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Marta Sanchez Castro
Database submission license No license selected
Created by Marta Sanchez Castro
Date created 2015-03-19 16:04:44 +01:00 (CET)
Date last edited 2015-05-05 20:35:31 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000034562 DNA arrayCGH blood - - 1 Marta Sanchez Castro


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