Variant #0000570112 (NC_000020.10:g.57484792C>T, NM_000516.4:c.772C>T (GNAS))

Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57484792C>T
DNA change (hg38) g.58909737C>T
Published as GNAS(NM_080425.3):c.2701C>T (p.R901W)
ISCN -
DB-ID GNAS_000034 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.772C>T r.(?) p.(Arg258Trp)
GNAS NM_016592.2 +/. - c.*678C>T r.(=) p.(=)
GNAS NM_080425.2 +/. - c.2701C>T r.(?) p.(Arg901Trp)


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