Variant #0000618221 (NC_000020.10:g.57415366C>A, NM_000516.4:c.-51416C>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.57415366C>A
DNA change (hg38) g.58840311C>A
Published as GNAS(NM_016592.2):c.205C>A (p.(His69Asn))
ISCN -
DB-ID GNAS_000457
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) 0.00037 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.-51416C>A r.(?) p.(=)
GNAS NM_016592.2 -?/. - c.205C>A r.(?) p.(His69Asn)
GNAS NM_080425.2 -?/. - c.-12955C>A r.(?) p.(=)
GNAS-AS1 NR_002785.2 -?/. - n.819+1626G>T r.(?) -


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