Variant #0000000451 (NC_000018.9:g.48575231G>A, NC_000018.9(NM_005359.5):c.424+1G>A (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.48575231G>A
Reference -
DB-ID SMAD4_000002
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 11:42:34 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
SMAD4 NM_005359.5 +/+ - c.424+1G>A r.spl? p.? -