Variant #0001049440 (NC_000020.10:g.57484420C>T, NM_000516.4:c.601C>T (GNAS))

Chromosome 20
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.57484420C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID GNAS_000026 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs11554273
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-21 11:37:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAS NM_000516.4 +/. - c.601C>T r.(?) p.(Arg201Cys)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.