Variant #0000935861 (NC_000016.9:g.56226205G>A, NM_020988.2:c.58G>A (GNAO1))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.56226205G>A
DNA change (hg38) g.56192293G>A
Published as -
ISCN -
DB-ID GNAO1_000056
Variant remarks -
Reference Journal: Saez Gonzalez 2023
ClinVar ID -
dbSNP ID rs2036182701
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.58G>A r.(?) p.(Glu20Lys)
GNAO1 NM_138736.2 ?/. - c.58G>A r.(?) p.(Glu20Lys)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.