Variant #0000000092 (NC_000021.8:g.27269956C>G, APP(NM_000484.3):c.1993G>C)

Individual ID 00000092
Chromosome 21
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.27269956C>G
Reference Peacock ML1, Murman DL, Sima AA, Warren JT Jr, Roses AD, Fink JK.(1994)
DB-ID APP_000001
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     
APP NM_000484.3 ./. 16 c.1993G>C r.(?) p.(Glu665Gln) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000092 ? ? APP 1 Y Yang