Variant #0000001526 (NC_000013.10:g.52544696A>G, ATP7B(NM_000053.3):c.1475T>C)

Individual ID 00001526
Chromosome 13
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52544696A>G
Reference Battisti C1, Dotti MT, Loudianos G, Dessì V, Battistini S, Amato T, Rufa A, Federico A.(2004)
DB-ID ATP7B_000018
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
ATP7B NM_000053.3 ./. 3 c.1475T>C r.(?) p.(Leu492Ser) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001526 ? ? ATP7B 1 Y Yang