Variant #0000052944 (NC_000020.10:g.57484251_57484254del)

Individual ID 00029521
Chromosome 20
Allele Maternal (inferred)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57484251_57484254del
DNA change (hg38) g.58909196_58909199del
Published as 565-568delGACT
ISCN -
DB-ID GNAS_000023 See all 26 reported entries
Variant remarks loss of function
Reference PubMed: Weinstein 1992
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation yes
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 2012-06-26 16:21:40 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000029564 DNA SEQ - - GNAS 1 Francesca Marta Elli


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