Variant #0000001547 (NC_000013.10:g.52532469C>A, ATP7B(NM_000053.3):c.2333G>T)

Individual ID 00001547
Chromosome 13
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52532469C>A
Reference Lee BH1, Kim JH, Lee SY, Jin HY, Kim KJ, Lee JJ, Park JY, Kim GH, Choi JH, Kim KM, Yoo HW.(2011)
DB-ID ATP7B_000004 See all 7 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00014 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
ATP7B NM_000053.3 ./. 8 c.2333G>T r.(?) p.(Arg778Leu) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001547 ? ? ATP7B 1 Y Yang