Variant #0001021333 (NC_000003.11:g.(?_292646)_(1143424_?)dup)

Individual ID 00460303
Chromosome 3
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.(?_292646)_(1143424_?)dup
DNA change (hg38) -
Published as -
ISCN 3p26;3(292646_1143424)x3
DB-ID chr3_007388
Variant remarks -
Reference PubMed: Karimi 2025
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 2025-01-23 10:24:30 +01:00 (CET)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000461935 DNA arrayCGH;arrayMET;SEQ;SEQ-NG - WES - 2 Johan den Dunnen


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