Variant #0000000452 (NC_000018.9:g.48581157C>G, NM_005359.5:c.461C>G (SMAD4))

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.48581157C>G
Reference -
DB-ID SMAD4_000003
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-10-02 11:43:18 +00:00 (UTC)
Date last edited 2025-11-17 10:50:59 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
SMAD4 NM_005359.5 +/+ - c.461C>G r.(?) p.(Ser154*) pathogenic