Variant #0000000672 (NC_000013.10:g.52511519A>G, NM_000053.3:c.3914T>C (ATP7B))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.52511519A>G
Reference -
DB-ID ATP7B_000021
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 2025-10-06 06:42:47 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
ATP7B NM_000053.3 +?/+? 19 c.3914T>C r.(?) p.(Leu1305Pro) likely pathogenic