Variant #0000983859 (NC_000020.10:g.57415579G>C, NM_000516.4:c.-51203G>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.57415579G>C
DNA change (hg38) -
Published as GNAS(NM_016592.5):c.418G>C (p.E140Q)
ISCN -
DB-ID GNAS-AS1_000020
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +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.-51203G>C r.(?) p.(=)
GNAS NM_016592.2 ?/. - c.418G>C r.(?) p.(Glu140Gln)
GNAS NM_080425.2 ?/. - c.-12742G>C r.(?) p.(=)
GNAS-AS1 NR_002785.2 ?/. - n.819+1413C>G r.(?) -


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