Variant #0000000194 (NC_000002.11:g.21229068G>A, NM_000384.2:c.10672C>T (APOB))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.21229068G>A
Reference -
DB-ID APOB_000005
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00034 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-27 12:19:31 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOB NM_000384.2 +/+ - c.10672C>T r.(?) p.(Arg3558Cys)