Variant #0000855882 (NC_000020.10:g.57415645C>A, NM_000516.4:c.-51137C>A (GNAS))

Chromosome 20
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.57415645C>A
DNA change (hg38) -
Published as GNAS(NM_016592.3):c.484C>A (p.R162S)
ISCN -
DB-ID GNAS-AS1_000015
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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.-51137C>A r.(?) p.(=)
GNAS NM_016592.2 ?/. - c.484C>A r.(?) p.(Arg162Ser)
GNAS NM_080425.2 ?/. - c.-12676C>A r.(?) p.(=)
GNAS-AS1 NR_002785.2 ?/. - n.819+1347G>T r.(?) -


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