Variant #0000061589 (NC_000002.11:g.(20402987_20403619)_(20451508_20452240)dup)

Individual ID 00034429
Chromosome 2
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.(20402987_20403619)_(20451508_20452240)dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr2_000756
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 01:10:27 +01:00 (CET)
Date last edited 2015-05-05 13:35:34 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000034496 DNA arrayCGH blood - - 1 Marta Sanchez Castro


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