Variant #0000989630 (NC_000010.10:g.(77700001_82000000)delN[(320000_460000)])

Individual ID 00453055
Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(77700001_82000000)delN[(320000_460000)]
DNA change (hg38) g.(75900001_80300000)delN[(320000_460000)]
Published as -
ISCN -
DB-ID chr10_005983
Variant remarks 0.32-0.46 Mb 10q22.3 duplication affecting SFPTD, PLAC9 and ANXA11
Reference PubMed: Rots 2024, Journal: Rots 2024
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
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 2024-08-15 20:40:59 +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     
0000454666 DNA SEQ-NG - - - 3 Johan den Dunnen


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