Variant #0000002266 (NC_000023.10:g.77264625C>A, ATP7A(NM_000052.6):c.1734C>A)

Individual ID 00002266
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.77264625C>A
Reference Tümer Z1, Lund C, Tolshave J, Vural B, T?nnesen T, Horn N.(1997)
DB-ID ATP7A_000044
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
ATP7A NM_000052.6 ./. 7 c.1734C>A r.(?) p.(Cys578*) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0015 protein truncation



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002266 ? ? ATP7A 1 Y Yang