Variant #0000909550 (NC_000013.10:g.52586149T>C, NM_000053.3:- (ATP7B))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.52586149T>C
DNA change (hg38) g.52012013T>C
Published as c.-676A>G
ISCN -
DB-ID ATP7B_000245 See all 15 reported entries
Variant remarks HepG2 cell expression cloning luciferase reporter assay show 0.34 reduced expression
Reference PubMed: Chen 2018
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-01-04 13:31:30 +01:00 (CET)
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 +/. _1 - r.(=|red) p.(=|red)


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