Variant #0000935776 (NC_000016.9:g.56226265G>T, NM_020988.2:c.118G>T (GNAO1))

Chromosome 16
Allele Unknown
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.56226265G>T
DNA change (hg38) g.56192353G>T
Published as -
ISCN -
DB-ID GNAO1_000067 See all 3 reported entries
Variant remarks -
Reference Journal: Saez Gonzalez 2023
ClinVar ID -
dbSNP ID rs886041715
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 2023-10-20 16:04:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAO1 NM_020988.2 +/. - c.118G>T r.(?) p.(Gly40Trp)
GNAO1 NM_138736.2 +/. - c.118G>T r.(?) p.(Gly40Trp)


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