Variant #0000001522 (NC_000013.10:g.52520549_52520557del9, ATP7B(NM_000053.3):c.2923_2931del9)

Individual ID 00001522
Chromosome 13
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52520549_52520557del9
Reference Okada T1, Morise T, Takeda Y, Mabuchi H.(2000)
DB-ID ATP7B_000058
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 ./. 13 c.2923_2931del9 r.(?) p.(Ser975_Thr977del) VariO:0141 DNA deletion VariO:0016 sequence retaining amino acid deletion



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001522 ? ? ATP7B 1 Y Yang