Variant #0000570051 (NC_000020.10:g.57428804A>G, NM_000516.4:c.-37978A>G (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.57428804A>G
DNA change (hg38) g.58853749A>G
Published as GNAS(NM_001077490.1):c.297A>G (p.(=)), GNAS(NM_080425.3):c.484A>G (p.M162V), GNAS(NM_080425.4):c.484A>G (p.M162V)
ISCN -
DB-ID GNAS_000351 See all 4 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) 0.0026 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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAS NM_000516.4 -?/. - c.-37978A>G r.(?) p.(=)
GNAS NM_016592.2 -?/. - c.*42+12863A>G r.(=) p.(=)
GNAS NM_080425.2 -?/. - c.484A>G r.(?) p.(Met162Val)


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