Variant #0000931189 (NC_000020.10:g.57428872T>C, NM_000516.4:c.-37910T>C (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.57428872T>C
DNA change (hg38) -
Published as GNAS(NM_001077490.1):c.365T>C (p.(Leu122Ser))
ISCN -
DB-ID GNAS_000553
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAS NM_000516.4 ?/. - c.-37910T>C r.(?) p.(=)
GNAS NM_016592.2 ?/. - c.*42+12931T>C r.(=) p.(=)
GNAS NM_080425.2 ?/. - c.552T>C r.(?) p.(=)


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