Variant #0000000622 (NC_000003.11:g.38645490G>A, NM_000335.4:c.1603C>T (SCN5A))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.38645490G>A
Reference -
DB-ID SCN5A_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2024-09-09 09:47:16 +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     
SCN5A NM_000335.4 +/+ - c.1603C>T r.(?) p.(Arg535*)