Variant #0000927029 (NC_000020.10:g.57415876C>A, NM_000516.4:c.-50906C>A (GNAS))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57415876C>A
DNA change (hg38) -
Published as GNAS(NM_001309861.1):c.-1093C>A (p.(=)), GNAS(NM_016592.4):c.715C>A (p.P239T), GNAS(NM_016592.5):c.715C>A (p.P239T)
ISCN -
DB-ID GNAS_000408 See all 3 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) 0.00295 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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.-50906C>A r.(?) p.(=)
GNAS NM_016592.2 -/. - c.715C>A r.(?) p.(Pro239Thr)
GNAS NM_080425.2 -/. - c.-12445C>A r.(?) p.(=)
GNAS-AS1 NR_002785.2 -/. - n.819+1116G>T r.(?) -


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