Variant #0000002262 (NC_000023.10:g.77253982_77253983insTGCCA, ATP7A(NM_000052.6):c.1344_1345insTGCCA)

Individual ID 00002262
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.77253982_77253983insTGCCA
Reference Tümer Z1, Lund C, Tolshave J, Vural B, T?nnesen T, Horn N.(1997)
DB-ID ATP7A_000040
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     
ATP7A NM_000052.6 ./. 5 c.1344_1345insTGCCA r.? p.? VariO:0142 DNA insertion -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002262 ? ? ATP7A 1 Y Yang