Variant #0000052828 (NC_000020.10:g.57484421G>A)

Individual ID 00029405
Chromosome 20
Allele Parent #1
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.57484421G>A
DNA change (hg38) g.58909366G>A
Published as 602G>A
ISCN -
DB-ID GNAS_000027 See all 5 reported entries
Variant remarks gain of function
Reference PubMed: Lyons 1990
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 2008-07-18 14:34:57 +02:00 (CEST)
Date last edited 2011-01-07 15:11:16 +01:00 (CET)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000029448 DNA SEQ - - GNAS 1 Johan den Dunnen


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