Variant #0000658783 (NC_000020.10:g.57415455C>T, NM_000516.4:c.-51327C>T (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.57415455C>T
DNA change (hg38) g.58840400C>T
Published as GNAS(NM_001309861.1):c.-1514C>T (p.(=)), GNAS(NM_016592.5):c.294C>T (p.P98=)
ISCN -
DB-ID GNAS_000401 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) 0.02989 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAS NM_000516.4 -?/. - c.-51327C>T r.(?) p.(=)
GNAS NM_016592.2 -?/. - c.294C>T r.(?) p.(Pro98=)
GNAS NM_080425.2 -?/. - c.-12866C>T r.(?) p.(=)
GNAS-AS1 NR_002785.2 -?/. - n.819+1537G>A r.(?) -


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