Variant #0000284738 (NC_000020.10:g.57428947G>A, NM_000516.4:c.-37835G>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.57428947G>A
DNA change (hg38) g.58853892G>A
Published as GNAS(NM_001077490.1):c.440G>A (p.(Arg147Lys)), GNAS(NM_001077490.2):c.440G>A (p.R147K), GNAS(NM_001077490.3):c.440G>A (p.R147K)
ISCN -
DB-ID GNAS_000354 See all 3 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) 0.008 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +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.-37835G>A r.(?) p.(=)
GNAS NM_016592.2 -/. - c.*42+13006G>A r.(=) p.(=)
GNAS NM_080425.2 -/. - c.627G>A r.(?) p.(Lys209=)


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