Variant #0000570041 (NC_000020.10:g.57415548_57415571del, NM_000516.4:c.-51234_-51211del (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.57415548_57415571del
DNA change (hg38) g.58840493_58840516del
Published as GNAS(NM_016592.2):c.382_405del (p.(Ala132_Thr139del))
ISCN -
DB-ID GNAS_000402
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAS NM_000516.4 -?/. - c.-51234_-51211del r.(?) p.(=)
GNAS NM_016592.2 -?/. - c.387_410del r.(?) p.(Ala132_Thr139del)
GNAS NM_080425.2 -?/. - c.-12773_-12750del r.(?) p.(=)
GNAS-AS1 NR_002785.2 -?/. - n.819+1426_819+1449del r.(?) -


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