Variant #0000061595 (NC_000009.11:g.(3735202_3781683)_(4161396_4258380)dup)

Individual ID 00034435
Chromosome 9
Allele Paternal (inferred)
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.(3735202_3781683)_(4161396_4258380)dup
DNA change (hg38) -
Published as g.(3735202_3781683)_(4161396_4258380)dup
ISCN -
DB-ID chr9_000457
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 01:33:53 +01:00 (CET)
Date last edited 2015-05-05 14:19:05 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000034502 DNA arrayCGH blood - - 1 Marta Sanchez Castro


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