Variant #0000693908 (NC_000017.10:g.(?_954760)_(1235739_?)dup)

Individual ID 00311169
Chromosome 17
Allele Unknown
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.(?_954760)_(1235739_?)dup
DNA change (hg38) -
Published as -
ISCN 17p13.3 (954,760-1,235,739)x3
DB-ID chr17_008082
Variant remarks -
Reference PubMed: Cristofoli 2020
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 2020-09-20 10:25:05 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000312323 DNA SEQ;SEQ-NG - WES LMNB1 2 Johan den Dunnen


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