Variant #0000000450 (NC_000018.9:g.48575235G>A, NC_000018.9(NM_005359.5):c.424+5G>A (SMAD4))

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.48575235G>A
Reference -
DB-ID SMAD4_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00021 View details
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 11:42:06 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

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