Variant #0000809293 (NC_000020.10:g.57428845T>C, NM_000516.4:c.-37937T>C (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.57428845T>C
DNA change (hg38) -
Published as GNAS(NM_001077490.1):c.338T>C (p.(Val113Ala)), GNAS(NM_001077490.3):c.338T>C (p.V113A)
ISCN -
DB-ID GNAS_000353 See all 2 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) 0.00175 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 2021-09-17 14:40:49 +02:00 (CEST)
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.-37937T>C r.(?) p.(=)
GNAS NM_016592.2 -/. - c.*42+12904T>C r.(=) p.(=)
GNAS NM_080425.2 -/. - c.525T>C r.(?) p.(Ser175=)


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