Variant #0000935773 (NC_000016.9:g.56226258_56226260del, NM_020988.2:c.111_113del (GNAO1))

Chromosome 16
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.56226258_56226260del
DNA change (hg38) g.56192346_56192348del
Published as -
ISCN -
DB-ID GNAO1_000063 See all 2 reported entries
Variant remarks -
Reference Journal: Saez Gonzalez 2023
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Harald Mikkers
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-08-14 14:11:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAO1 NM_020988.2 +?/. - c.111_113del r.(?) p.(Leu39del)
GNAO1 NM_138736.2 +?/. - c.111_113del r.(?) p.(Leu39del)


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