Variant #0000052884 (NC_000020.10:g.57478620_57478622del)

Individual ID 00029461
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.57478620_57478622del
DNA change (hg38) g.58903565_58903567del
Published as -
ISCN -
DB-ID GNAS_000073
Variant remarks loss of function
Reference J Clin Endocrinol Metab 92, 1073
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Francesca Marta Elli
Database submission license No license selected
Created by Francesca Marta Elli
Date created 2012-05-21 13:39:16 +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     
0000029504 DNA SEQ - - GNAS 1 Francesca Marta Elli


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