Variant #0000693008 (NC_000020.10:g.57415698G>A, NM_000516.4:c.-51084G>A (GNAS))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57415698G>A
DNA change (hg38) -
Published as GNAS(NM_016592.3):c.537G>A (p.P179=), GNAS(NM_016592.5):c.537G>A (p.P179=)
ISCN -
DB-ID GNAS_000458 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) 0.00072 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 2023-01-11 15:44:22 +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.-51084G>A r.(?) p.(=)
GNAS NM_016592.2 -?/. - c.537G>A r.(?) p.(Pro179=)
GNAS NM_080425.2 -?/. - c.-12623G>A r.(?) p.(=)
GNAS-AS1 NR_002785.2 -?/. - n.819+1294C>T r.(?) -


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