Variant #0000001600 (NC_000013.10:g.52532508T>C, ATP7B(NM_000053.3):c.2294A>G)

Individual ID 00001600
Chromosome 13
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52532508T>C
Reference Wei Z1, Huang Y, Liu A, Diao S, Yu Q, Peng Z, Hong M.(2014)
DB-ID ATP7B_000084
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 ./. 8 c.2294A>G r.(?) p.(Asp765Gly) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001600 ? ? ATP7B 1 Y Yang