Variant #0000004776 (NC_000021.8:g.27284122T>C, APP(NM_000484.3):c.1840A>G)

Individual ID 00004776
Chromosome 21
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.27284122T>C
Reference Lee JH et al. (2014)
DB-ID APP_000025
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00103 View details
Owner XY Liu
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by XY Liu
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
APP NM_000484.3 ./. 14 c.1840A>G r.(?) p.(Ser614Gly) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000004776 ? ? APP 1 XY Liu