Variant #0000281099 (NC_000020.10:g.57429040G>A, NM_000516.4:c.-37742G>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.57429040G>A
DNA change (hg38) g.58853985G>A
Published as GNAS(NM_001077490.3):c.533G>A (p.R178Q)
ISCN -
DB-ID GNAS_000357
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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.-37742G>A r.(?) p.(=)
GNAS NM_016592.2 ?/. - c.*42+13099G>A r.(=) p.(=)
GNAS NM_080425.2 ?/. - c.720G>A r.(?) p.(Pro240=)


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