Variant #0000001557 (NC_000013.10:g.52535985A>C, ATP7B(NM_000053.3):c.1934T>G)

Individual ID 00001557
Chromosome 13
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52535985A>C
Reference Usta J1, Abu Daya H, Halawi H, Al-Shareef I, El-Rifai O, Malli AH, Sharara AI, Habib RH, Barada K.(2012)
DB-ID ATP7B_000011 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00052 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 ./. 6 c.1934T>G r.(?) p.(Met645Arg) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001557 ? ? ATP7B 1 Y Yang