Variant #0000000732 (NC_000019.9:g.11222220G>A, NM_000527.4:c.1091G>A (LDLR))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.11222220G>A
Reference -
DB-ID LDLR_000008
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 2026-06-29 05:45:09 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
LDLR NM_000527.4 +/+ - c.1091G>A r.(?) p.(Cys364Tyr) pathogenic