Variant #0000050406 (NC_000020.10:g.57464811|bsrC)

Individual ID 00027197
Chromosome 20
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57464811|bsrC
DNA change (hg38) -
Published as GNAS-DMR CG8
ISCN -
DB-ID GNAS_000227
Variant remarks normal methylation GNAS-DMR
Reference PubMed: Kagami 2014
ClinVar ID -
dbSNP ID -
Origin Somatic
Segregation -
Frequency -
Re-site -
VIP -
Methylation 0.35 (controls 0.30-0.37)
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 2014-12-29 15:45:33 +01:00 (CET)
Date last edited 2017-05-05 13:19:20 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000027203 DNA SEQp leukocytes - GNAS, H19, KCNQ1, MEG3, MEST, PLAGL1, SNRPN 49 Johan den Dunnen


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