Variant #0000570046 (NC_000020.10:g.57415812T>A, NM_000516.4:c.-50970T>A (GNAS))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57415812T>A
DNA change (hg38) g.58840757T>A
Published as GNAS(NM_016592.5):c.651T>A (p.R217=)
ISCN -
DB-ID GNAS_000407
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) 0.00627 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAS NM_000516.4 -/. - c.-50970T>A r.(?) p.(=)
GNAS NM_016592.2 -/. - c.651T>A r.(?) p.(Arg217=)
GNAS NM_080425.2 -/. - c.-12509T>A r.(?) p.(=)
GNAS-AS1 NR_002785.2 -/. - n.819+1180A>T r.(?) -


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