Variant #0000811353 (NC_000012.11:g.(?_24692382)_(25353987_?)dup)

Individual ID 00383379
Chromosome 12
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.(?_24692382)_(25353987_?)dup
DNA change (hg38) -
Published as 12p12.1:24,692,382– 25,353,987
ISCN -
DB-ID chr12_007251
Variant remarks -
Reference PubMed: Marom 2021
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 2021-09-29 09:35:05 +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     
0000384608 DNA arrayCGH - - - 1 Johan den Dunnen


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