Variant #0000866535 (NC_000020.10:g.57415536C>G, NM_000516.4:c.-51246C>G (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.57415536C>G
DNA change (hg38) -
Published as GNAS(NM_016592.3):c.375C>G (p.F125L)
ISCN -
DB-ID GNAS-AS1_000014
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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.-51246C>G r.(?) p.(=)
GNAS NM_016592.2 -?/. - c.375C>G r.(?) p.(Phe125Leu)
GNAS NM_080425.2 -?/. - c.-12785C>G r.(?) p.(=)
GNAS-AS1 NR_002785.2 -?/. - n.819+1456G>C r.(?) -


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