Variant #0000624177 (NC_000020.10:g.57429067C>A, NM_000516.4:c.-37715C>A (GNAS))

Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57429067C>A
DNA change (hg38) g.58854012C>A
Published as GNAS(NM_001077490.2):c.560C>A (p.S187*)
ISCN -
DB-ID GNAS_000461
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-16 18:49:03 +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.-37715C>A r.(?) p.(=)
GNAS NM_016592.2 +/. - c.*42+13126C>A r.(=) p.(=)
GNAS NM_080425.2 +/. - c.747C>A r.(?) p.(Val249=)


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