Variant #0000693009 (NC_000020.10:g.57428997T>C, NM_000516.4:c.-37785T>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.57428997T>C
DNA change (hg38) -
Published as GNAS(NM_001077490.2):c.490T>C (p.L164=), GNAS(NM_080425.3):c.677T>C (p.F226S)
ISCN -
DB-ID GNAS_000491
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) 3.0E-5 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAS NM_000516.4 ?/. - c.-37785T>C r.(?) p.(=)
GNAS NM_016592.2 ?/. - c.*42+13056T>C r.(=) p.(=)
GNAS NM_080425.2 ?/. - c.677T>C r.(?) p.(Phe226Ser)


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