Variant #0000000180 (NC_000013.10:g.52534410C>T, NM_000053.3:c.1995G>A (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.52534410C>T
Reference -
DB-ID ATP7B_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00146 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 11:54:18 +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     
ATP7B NM_000053.3 +?/+? 7 c.1995G>A r.(?) p.(Met665Ile)