Variant #0000787125 (NC_000008.10:g.(?_1496860)_(6728348_?)del)

Individual ID 00374580
Chromosome 8
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.(?_1496860)_(6728348_?)del
DNA change (hg38) -
Published as chr8:1496860-?_6728348+?del
ISCN -
DB-ID chr8_005229
Variant remarks del incl. DLGAP2, CLN8, ARHGEF10, CSMD1, MCPH1 and DEFB1
Reference PubMed: Ganapathy 2019
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 2021-05-24 20:06:48 +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     
0000375774 DNA SEQ-NG - TruSight One panel - 2 Johan den Dunnen


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