Variant #0000670373 (NC_000015.9:g.(?_22770421)_(23282799_?)del)

Individual ID 00305552
Chromosome 15
Allele Paternal (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.(?_22770421)_(23282799_?)del
DNA change (hg38) -
Published as chr15:22770421-23282799
ISCN 15q11.2del
DB-ID chr15_005419
Variant remarks -
Reference PubMed: Vissers 2020
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 2020-06-28 11:11:46 +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     
0000306681 DNA SEQ;SEQ-NG - WES CNOT1 3 Johan den Dunnen


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