Variant #0000931814 (NC_000008.10:g.(?_10066633)_(10780057_?)dup)

Individual ID 00435579
Chromosome 8
Allele Maternal (confirmed)
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.(?_10066633)_(10780057_?)dup
DNA change (hg38) -
Published as chr810,066,633–10,780,057x3
ISCN -
DB-ID chr8_005612
Variant remarks -
Reference PubMed: Bramswig 2017
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-08-04 19:08:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000437058 DNA arrayCGH;SEQ;SEQ-NG - WES - 3 Johan den Dunnen


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