Variant #0000915409 (NC_000020.10:g.57428516G>A, NM_000516.4:c.-38266G>A (GNAS))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57428516G>A
DNA change (hg38) -
Published as GNAS(NM_001077490.1):c.9G>A (p.(=)), GNAS(NM_080425.3):c.196G>A (p.E66K), GNAS(NM_080425.4):c.196G>A (p.E66K)
ISCN -
DB-ID GNAS_000482 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00032 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.-38266G>A r.(?) p.(=)
GNAS NM_016592.2 -?/. - c.*42+12575G>A r.(=) p.(=)
GNAS NM_080425.2 -?/. - c.196G>A r.(?) p.(Glu66Lys)


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