Variant #0000288539 (NC_000020.10:g.57428998T>G, NM_000516.4:c.-37784T>G (GNAS))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57428998T>G
DNA change (hg38) g.58853943T>G
Published as GNAS(NM_001077490.2):c.491T>G (p.L164W), GNAS(NM_080425.4):c.678T>G (p.(Phe226Leu))
ISCN -
DB-ID GNAS_000356 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) 0.0001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.-37784T>G r.(?) p.(=)
GNAS NM_016592.2 ?/. - c.*42+13057T>G r.(=) p.(=)
GNAS NM_080425.2 ?/. - c.678T>G r.(?) p.(Phe226Leu)


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