Variant #0000000192 (NC_000002.11:g.21229160C>A, APOB(NM_000384.2):c.10580G>T)

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.21229160C>A
Reference -
DB-ID APOB_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOB NM_000384.2 +/+ - c.10580G>T r.(?) p.(Arg3527Leu)