Variant #0000328507 (NC_000020.10:g.57415559C>T, NM_000516.4:c.-51223C>T (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.57415559C>T
DNA change (hg38) g.58840504C>T
Published as GNAS(NM_016592.3):c.398C>T (p.P133L), GNAS(NM_016592.5):c.398C>T (p.P133L, p.(Pro133Leu))
ISCN -
DB-ID GNAS-AS1_000001 See all 4 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) 6.0E-5 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 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.-51223C>T r.(?) p.(=)
GNAS NM_016592.2 ?/. - c.398C>T r.(?) p.(Pro133Leu)
GNAS NM_080425.2 ?/. - c.-12762C>T r.(?) p.(=)
GNAS-AS1 NR_002785.2 ?/. - n.819+1433G>A r.(?) -


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